AKAP12 | APKFKFRAL | ENDOMETRIUM | 1407 | p.E1403fs | c.4209_4209delG | Frame_Shift_Del | 5 | 0.11 | EN | Y | 16 | 12 | 0 | N |
AKAP12 | CLGQERQYA | ENDOMETRIUM | 1399 | p.E1403fs | c.4209_4209delG | Frame_Shift_Del | 4 | 0.11 | EN | N | 2 | 0 | 0 | N |
AKAP12 | ERQYAPKFK | ENDOMETRIUM | 1403 | p.E1403fs | c.4209_4209delG | Frame_Shift_Del | 5 | 0.11 | EN | N | 1 | 0 | 0 | Y |
AKAP12 | FKFRALRHH | ENDOMETRIUM | 1410 | p.E1403fs | c.4209_4209delG | Frame_Shift_Del | 5 | 0.11 | EN | N | 3 | 0 | 17 | N |
AKAP12 | FRALRHHSL | ENDOMETRIUM | 1412 | p.E1403fs | c.4209_4209delG | Frame_Shift_Del | 5 | 0.11 | EN | Y | 9 | 10 | 17 | N |
AKAP12 | GQERQYAPK | ENDOMETRIUM | 1401 | p.E1403fs | c.4209_4209delG | Frame_Shift_Del | 5 | 0.11 | EN | N | 4 | 0 | 0 | N |
AKAP12 | KFKFRALRH | ENDOMETRIUM | 1409 | p.E1403fs | c.4209_4209delG | Frame_Shift_Del | 5 | 0.11 | EN | Y | 1 | 14 | 0 | N |
AKAP12 | KFRALRHHS | ENDOMETRIUM | 1411 | p.E1403fs | c.4209_4209delG | Frame_Shift_Del | 4 | 0.11 | EN | N | 1 | 0 | 0 | N |
AKAP12 | KNQSPSWKR | ENDOMETRIUM | 770 | p.R769fs | c.2307_2307delA | Frame_Shift_Del | 5 | 0.11 | HEC108 | N | 3 | 0 | 0 | N |
AKAP12 | KRLVTPRKN | ENDOMETRIUM | 763 | p.R769fs | c.2307_2307delA | Frame_Shift_Del | 1 | 0.11 | HEC108 | N | 2 | 0 | 0 | N |
AKAP12 | KVLSKPPKA | LARGE_INTESTINE | 487 | p.P492fs | c.1474_1474delC | Frame_Shift_Del | 2 | 0.11 | SNUC2A | N | 5 | 0 | 0 | N |
AKAP12 | LGQERQYAP | ENDOMETRIUM | 1400 | p.E1403fs | c.4209_4209delG | Frame_Shift_Del | 5 | 0.11 | EN | N | 1 | 0 | 0 | N |
AKAP12 | LVTPRKNQS | ENDOMETRIUM | 765 | p.R769fs | c.2307_2307delA | Frame_Shift_Del | 3 | 0.11 | HEC108 | N | 0 | 0 | 21 | N |
AKAP12 | NQSPSWKRK | ENDOMETRIUM | 771 | p.R769fs | c.2307_2307delA | Frame_Shift_Del | 5 | 0.11 | HEC108 | Y | 3 | 13 | 0 | N |
AKAP12 | PCLGQERQY | ENDOMETRIUM | 1398 | p.E1403fs | c.4209_4209delG | Frame_Shift_Del | 3 | 0.11 | EN | N | 0 | 0 | 0 | N |
AKAP12 | PKFKFRALR | ENDOMETRIUM | 1408 | p.E1403fs | c.4209_4209delG | Frame_Shift_Del | 5 | 0.11 | EN | N | 1 | 0 | 0 | N |
AKAP12 | PPCLGQERQ | ENDOMETRIUM | 1397 | p.E1403fs | c.4209_4209delG | Frame_Shift_Del | 2 | 0.11 | EN | N | 0 | 0 | 0 | N |
AKAP12 | PPPCLGQER | ENDOMETRIUM | 1396 | p.E1403fs | c.4209_4209delG | Frame_Shift_Del | 1 | 0.11 | EN | N | 0 | 0 | 0 | N |
AKAP12 | PRKNQSPSW | ENDOMETRIUM | 768 | p.R769fs | c.2307_2307delA | Frame_Shift_Del | 5 | 0.11 | HEC108 | N | 1 | 0 | 0 | N |
AKAP12 | PSWKRKAKT | ENDOMETRIUM | 774 | p.R769fs | c.2307_2307delA | Frame_Shift_Del | 5 | 0.11 | HEC108 | N | 0 | 0 | 0 | N |
AKAP12 | QERQYAPKF | ENDOMETRIUM | 1402 | p.E1403fs | c.4209_4209delG | Frame_Shift_Del | 5 | 0.11 | EN | N | 5 | 0 | 0 | N |
AKAP12 | QSPSWKRKA | ENDOMETRIUM | 772 | p.R769fs | c.2307_2307delA | Frame_Shift_Del | 5 | 0.11 | HEC108 | N | 1 | 0 | 0 | N |
AKAP12 | QYAPKFKFR | ENDOMETRIUM | 1405 | p.E1403fs | c.4209_4209delG | Frame_Shift_Del | 6 | 0.11 | EN | Y | 2 | 11 | 0 | N |
AKAP12 | RKNQSPSWK | ENDOMETRIUM | 769 | p.R769fs | c.2307_2307delA | Frame_Shift_Del | 5 | 0.11 | HEC108 | N | 1 | 0 | 0 | N |
AKAP12 | RLVTPRKNQ | ENDOMETRIUM | 764 | p.R769fs | c.2307_2307delA | Frame_Shift_Del | 2 | 0.11 | HEC108 | N | 0 | 0 | 0 | N |
AKAP12 | RQYAPKFKF | ENDOMETRIUM | 1404 | p.E1403fs | c.4209_4209delG | Frame_Shift_Del | 6 | 0.11 | EN | N | 12 | 0 | 0 | N |
AKAP12 | SPSWKRKAK | ENDOMETRIUM | 773 | p.R769fs | c.2307_2307delA | Frame_Shift_Del | 5 | 0.11 | HEC108 | Y | 1 | 10 | 0 | N |
AKAP12 | SWKRKAKTP | ENDOMETRIUM | 775 | p.R769fs | c.2307_2307delA | Frame_Shift_Del | 4 | 0.11 | HEC108 | N | 0 | 0 | 0 | N |
AKAP12 | TPRKNQSPS | ENDOMETRIUM | 767 | p.R769fs | c.2307_2307delA | Frame_Shift_Del | 5 | 0.11 | HEC108 | N | 5 | 0 | 0 | N |
AKAP12 | VLSKPPKAL | LARGE_INTESTINE | 488 | p.P492fs | c.1474_1474delC | Frame_Shift_Del | 3 | 0.11 | SNUC2A | N | 9 | 0 | 5 | N |
AKAP12 | VTPRKNQSP | ENDOMETRIUM | 766 | p.R769fs | c.2307_2307delA | Frame_Shift_Del | 4 | 0.11 | HEC108 | N | 0 | 0 | 1 | N |
AKAP12 | YAPKFKFRA | ENDOMETRIUM | 1406 | p.E1403fs | c.4209_4209delG | Frame_Shift_Del | 6 | 0.11 | EN | N | 8 | 0 | 12 | N |
AKAP12 | EKVLSKPPK | LARGE_INTESTINE | 486 | p.P492fs | c.1474_1474delC | Frame_Shift_Del | 1 | 0.22 | SNUC2A | N | 1 | 0 | 0 | N |
AKAP12 | ASGTQSGGH | LARGE_INTESTINE | 1201 | p.S1206fs | c.3618_3619insG | Frame_Shift_Ins | 1 | 0.11 | RKO | N | 0 | 0 | 0 | N |
AKAP12 | ASSTFQFCV | LARGE_INTESTINE | 1221 | p.S1206fs | c.3618_3619insG | Frame_Shift_Ins | 5 | 0.11 | RKO | N | 6 | 0 | 0 | Y |
AKAP12 | CTEREASST | LARGE_INTESTINE | 1216 | p.S1206fs | c.3618_3619insG | Frame_Shift_Ins | 4 | 0.11 | RKO | N | 1 | 0 | 0 | N |
AKAP12 | EASSTFQFC | LARGE_INTESTINE | 1220 | p.S1206fs | c.3618_3619insG | Frame_Shift_Ins | 5 | 0.11 | RKO | N | 2 | 0 | 0 | Y |
AKAP12 | EREASSTFQ | LARGE_INTESTINE | 1218 | p.S1206fs | c.3618_3619insG | Frame_Shift_Ins | 5 | 0.11 | RKO | N | 0 | 0 | 0 | N |
AKAP12 | FQFCVPGRN | LARGE_INTESTINE | 1225 | p.S1206fs | c.3618_3619insG | Frame_Shift_Ins | 6 | 0.11 | RKO | N | 4 | 0 | 5 | N |
AKAP12 | GGHRSRGSS | LARGE_INTESTINE | 1207 | p.S1206fs | c.3618_3619insG | Frame_Shift_Ins | 5 | 0.11 | RKO | N | 0 | 0 | 0 | N |
AKAP12 | GHRSRGSSC | LARGE_INTESTINE | 1208 | p.S1206fs | c.3618_3619insG | Frame_Shift_Ins | 5 | 0.11 | RKO | N | 0 | 0 | 0 | N |
AKAP12 | GSSCTEREA | LARGE_INTESTINE | 1213 | p.S1206fs | c.3618_3619insG | Frame_Shift_Ins | 4 | 0.11 | RKO | N | 1 | 0 | 0 | N |
AKAP12 | GTQSGGHRS | LARGE_INTESTINE | 1203 | p.S1206fs | c.3618_3619insG | Frame_Shift_Ins | 3 | 0.11 | RKO | N | 0 | 0 | 0 | N |
AKAP12 | HRSRGSSCT | LARGE_INTESTINE | 1209 | p.S1206fs | c.3618_3619insG | Frame_Shift_Ins | 5 | 0.11 | RKO | N | 2 | 0 | 0 | N |
AKAP12 | QSGGHRSRG | LARGE_INTESTINE | 1205 | p.S1206fs | c.3618_3619insG | Frame_Shift_Ins | 5 | 0.11 | RKO | N | 0 | 0 | 0 | N |
AKAP12 | REASSTFQF | LARGE_INTESTINE | 1219 | p.S1206fs | c.3618_3619insG | Frame_Shift_Ins | 5 | 0.11 | RKO | Y | 10 | 10 | 0 | Y |
AKAP12 | RGSSCTERE | LARGE_INTESTINE | 1212 | p.S1206fs | c.3618_3619insG | Frame_Shift_Ins | 4 | 0.11 | RKO | N | 0 | 0 | 0 | N |
AKAP12 | RSRGSSCTE | LARGE_INTESTINE | 1210 | p.S1206fs | c.3618_3619insG | Frame_Shift_Ins | 4 | 0.11 | RKO | N | 0 | 0 | 0 | N |
AKAP12 | SCTEREASS | LARGE_INTESTINE | 1215 | p.S1206fs | c.3618_3619insG | Frame_Shift_Ins | 4 | 0.11 | RKO | N | 1 | 0 | 0 | N |
AKAP12 | SGGHRSRGS | LARGE_INTESTINE | 1206 | p.S1206fs | c.3618_3619insG | Frame_Shift_Ins | 5 | 0.11 | RKO | N | 1 | 0 | 0 | N |
AKAP12 | SGTQSGGHR | LARGE_INTESTINE | 1202 | p.S1206fs | c.3618_3619insG | Frame_Shift_Ins | 2 | 0.11 | RKO | N | 1 | 0 | 0 | N |
AKAP12 | SRGSSCTER | LARGE_INTESTINE | 1211 | p.S1206fs | c.3618_3619insG | Frame_Shift_Ins | 4 | 0.11 | RKO | Y | 3 | 9 | 0 | N |
AKAP12 | SSCTEREAS | LARGE_INTESTINE | 1214 | p.S1206fs | c.3618_3619insG | Frame_Shift_Ins | 4 | 0.11 | RKO | N | 0 | 0 | 0 | N |
AKAP12 | SSTFQFCVP | LARGE_INTESTINE | 1222 | p.S1206fs | c.3618_3619insG | Frame_Shift_Ins | 5 | 0.11 | RKO | N | 0 | 0 | 0 | Y |
AKAP12 | STFQFCVPG | LARGE_INTESTINE | 1223 | p.S1206fs | c.3618_3619insG | Frame_Shift_Ins | 6 | 0.11 | RKO | N | 0 | 0 | 0 | N |
AKAP12 | TEREASSTF | LARGE_INTESTINE | 1217 | p.S1206fs | c.3618_3619insG | Frame_Shift_Ins | 4 | 0.11 | RKO | N | 6 | 0 | 0 | N |
AKAP12 | TFQFCVPGR | LARGE_INTESTINE | 1224 | p.S1206fs | c.3618_3619insG | Frame_Shift_Ins | 6 | 0.11 | RKO | N | 2 | 0 | 0 | N |
AKAP12 | TQSGGHRSR | LARGE_INTESTINE | 1204 | p.S1206fs | c.3618_3619insG | Frame_Shift_Ins | 4 | 0.11 | RKO | N | 4 | 0 | 0 | N |
AKAP12 | AASKESESK | PROSTATE | 225 | p.P232S | c.694C>T | Missense_Mutation | 1 | 0.11 | DU145 | N | 1 | 0 | 0 | N |
AKAP12 | AASKESKPK | LARGE_INTESTINE | 225 | p.E231K | c.691G>A | Missense_Mutation | 1 | 0.11 | SNU81 | N | 0 | 0 | 0 | N |
AKAP12 | ADFPDSQEE | ENDOMETRIUM | 552 | p.S554F | c.1661C>T | Missense_Mutation | 1 | 0.11 | JHUEM7 | N | 0 | 0 | 0 | N |
AKAP12 | ADLSPDEMV | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 480 | p.K487M | c.1460A>T | Missense_Mutation | 1 | 0.11 | KMS34 | N | 6 | 0 | 0 | N |
AKAP12 | ADVSPDEKV | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 480 | p.L482V | c.1444C>G | Missense_Mutation | 1 | 0.11 | HT | N | 5 | 0 | 0 | N |
AKAP12 | AEAQRPEEQ | LUNG | 1072 | p.E1075Q | c.3223G>C | Missense_Mutation | 1 | 0.11 | HCC78 | N | 2 | 0 | 0 | N |
AKAP12 | AEKGATSDG | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 592 | p.E594K | c.1780G>A | Missense_Mutation | 1 | 0.11 | MOLT13 | N | 1 | 0 | 0 | N |
AKAP12 | AEPTYVNEE | LARGE_INTESTINE | 1348 | p.H1352Y | c.4054C>T | Missense_Mutation | 1 | 0.11 | LS123 | N | 1 | 0 | 0 | N |
AKAP12 | AEVVSEKLT | ENDOMETRIUM | 343 | p.A346V | c.1037C>T | Missense_Mutation | 1 | 0.11 | MFE319 | N | 6 | 0 | 0 | N |
AKAP12 | AGSQEHDTG | ENDOMETRIUM | 730 | p.P737T | c.2209C>A | Missense_Mutation | 1 | 0.11 | HEC251 | N | 0 | 0 | 0 | N |
AKAP12 | AHSDISKDR | ENDOMETRIUM | 1626 | p.M1634R | c.4901T>G | Missense_Mutation | 1 | 0.11 | HEC6 | N | 1 | 0 | 0 | Y |
AKAP12 | AHVIKANSQ | LUNG | 1580 | p.D1586N | c.4756G>A | Missense_Mutation | 1 | 0.11 | NCIH23 | N | 0 | 0 | 0 | N |
AKAP12 | AIEDLEPQN | LUNG | 1529 | p.E1536Q | c.4606G>C | Missense_Mutation | 1 | 0.11 | NCIH23 | N | 1 | 0 | 0 | N |
AKAP12 | ALELHSHAK | LUNG | 1319 | p.Q1323H | c.3969G>T | Missense_Mutation | 1 | 0.11 | NCIH2106 | N | 5 | 0 | 0 | N |
AKAP12 | ALTDTDASG | PROSTATE | 1713 | p.A1715T | c.5143G>A | Missense_Mutation | 1 | 0.11 | 22RV1 | N | 0 | 0 | 0 | N |
AKAP12 | AMVPLSEYD | CENTRAL_NERVOUS_SYSTEM | 845 | p.V846M | c.2536G>A | Missense_Mutation | 1 | 0.11 | LN18 | N | 1 | 0 | 0 | N |
AKAP12 | ANSQDAGQE | LUNG | 1585 | p.D1586N | c.4756G>A | Missense_Mutation | 1 | 0.11 | NCIH23 | N | 0 | 0 | 0 | N |
AKAP12 | APQVTENIE | LARGE_INTESTINE | 1123 | p.S1129N | c.3386G>A | Missense_Mutation | 1 | 0.11 | KM12 | N | 0 | 0 | 0 | Y |
AKAP12 | AQLAQKSAE | LUNG | 862 | p.Q864L | c.2591A>T | Missense_Mutation | 1 | 0.11 | NCIH23 | N | 0 | 0 | 0 | N |
AKAP12 | AQRPEEQAE | LUNG | 1074 | p.E1075Q | c.3223G>C | Missense_Mutation | 1 | 0.11 | HCC78 | N | 0 | 0 | 0 | N |
AKAP12 | ARRWSSSDE | ENDOMETRIUM | 692 | p.G695W | c.2083G>T | Missense_Mutation | 1 | 0.11 | SNGM | N | 1 | 0 | 0 | N |
AKAP12 | ARSDISKDM | LARGE_INTESTINE | 1626 | p.H1627R | c.4880A>G | Missense_Mutation | 1 | 0.11 | CL11 | Y | 4 | 9 | 0 | N |
AKAP12 | ASGTQSGDT | ENDOMETRIUM | 1201 | p.G1208D | c.3623G>A | Missense_Mutation | 1 | 0.11 | HEC1B | N | 1 | 0 | 0 | N |
AKAP12 | ASKESESKQ | PROSTATE | 226 | p.P232S | c.694C>T | Missense_Mutation | 1 | 0.11 | DU145 | N | 0 | 0 | 0 | N |
AKAP12 | ASKESKPKQ | LARGE_INTESTINE | 226 | p.E231K | c.691G>A | Missense_Mutation | 1 | 0.11 | SNU81 | N | 0 | 0 | 0 | N |
AKAP12 | ATKSAVDHD | UPPER_AERODIGESTIVE_TRACT | 125 | p.V131D | c.392T>A | Missense_Mutation | 1 | 0.11 | SNU46 | N | 0 | 0 | 0 | N |
AKAP12 | ATTKKGLSF | SKIN | 1490 | p.S1498F | c.4493C>T | Missense_Mutation | 1 | 0.11 | MEWO | N | 4 | 0 | 0 | N |
AKAP12 | AVDHDITDD | UPPER_AERODIGESTIVE_TRACT | 129 | p.V131D | c.392T>A | Missense_Mutation | 1 | 0.11 | SNU46 | N | 0 | 0 | 0 | N |
AKAP12 | AVEMEKMEA | LARGE_INTESTINE | 854 | p.R857M | c.2570G>T | Missense_Mutation | 1 | 0.11 | CW2 | N | 1 | 0 | 0 | N |
AKAP12 | AVGQARSDI | LARGE_INTESTINE | 1622 | p.H1627R | c.4880A>G | Missense_Mutation | 1 | 0.11 | CL11 | N | 5 | 0 | 0 | N |
AKAP12 | AVVLLSEYD | UPPER_AERODIGESTIVE_TRACT | 845 | p.P848L | c.2543C>T | Missense_Mutation | 1 | 0.11 | HS840T | N | 0 | 0 | 0 | N |
AKAP12 | CLEKGLDEV | LUNG | 578 | p.A584D | c.1751C>A | Missense_Mutation | 1 | 0.11 | SW1271 | N | 2 | 0 | 0 | N |
AKAP12 | CVSREDPTQ | LIVER | 470 | p.G473R | c.1417G>A | Missense_Mutation | 1 | 0.11 | SNU449 | N | 0 | 0 | 0 | Y |
AKAP12 | DALELHSHA | LUNG | 1318 | p.Q1323H | c.3969G>T | Missense_Mutation | 1 | 0.11 | NCIH2106 | N | 4 | 0 | 0 | N |
AKAP12 | DAVEMEKME | LARGE_INTESTINE | 853 | p.R857M | c.2570G>T | Missense_Mutation | 1 | 0.11 | CW2 | N | 0 | 0 | 0 | N |
AKAP12 | DDALELHSH | LUNG | 1317 | p.Q1323H | c.3969G>T | Missense_Mutation | 1 | 0.11 | NCIH2106 | N | 0 | 0 | 0 | N |
AKAP12 | DDGQKETPE | SKIN | 136 | p.E140K | c.418G>A | Missense_Mutation | 1 | 0.11 | MEWO | N | 0 | 0 | 0 | N |
AKAP12 | DDSDVPAMV | CENTRAL_NERVOUS_SYSTEM | 839 | p.V846M | c.2536G>A | Missense_Mutation | 1 | 0.11 | LN18 | N | 4 | 0 | 0 | N |
AKAP12 | DEESGEHTR | STOMACH | 541 | p.Q549R | c.1646A>G | Missense_Mutation | 1 | 0.11 | 2313287 | Y | 2 | 9 | 0 | N |
AKAP12 | DEKIDVHQE | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 405 | p.E409D | c.1227A>T | Missense_Mutation | 1 | 0.11 | WSUDLCL2 | N | 1 | 0 | 0 | N |
AKAP12 | DEMVLSKPP | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 485 | p.K487M | c.1460A>T | Missense_Mutation | 1 | 0.11 | KMS34 | N | 1 | 0 | 0 | N |
AKAP12 | DEVQQDGEA | LUNG | 584 | p.A584D | c.1751C>A | Missense_Mutation | 1 | 0.11 | SW1271 | N | 5 | 0 | 0 | N |
AKAP12 | DFPDSQEEQ | ENDOMETRIUM | 553 | p.S554F | c.1661C>T | Missense_Mutation | 1 | 0.11 | JHUEM7 | N | 0 | 0 | 0 | N |
AKAP12 | DGEAEKGAT | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 589 | p.E594K | c.1780G>A | Missense_Mutation | 1 | 0.11 | MOLT13 | N | 0 | 0 | 0 | N |
AKAP12 | DGKAEVVSE | ENDOMETRIUM | 340 | p.A346V | c.1037C>T | Missense_Mutation | 1 | 0.11 | MFE319 | N | 0 | 0 | 0 | N |
AKAP12 | DGQKETPEI | SKIN | 137 | p.E140K | c.418G>A | Missense_Mutation | 1 | 0.11 | MEWO | N | 6 | 0 | 0 | N |
AKAP12 | DHDITDDGQ | UPPER_AERODIGESTIVE_TRACT | 131 | p.V131D | c.392T>A | Missense_Mutation | 1 | 0.11 | SNU46 | N | 0 | 0 | 0 | N |
AKAP12 | DISKDRSEA | ENDOMETRIUM | 1629 | p.M1634R | c.4901T>G | Missense_Mutation | 1 | 0.11 | HEC6 | N | 1 | 0 | 0 | N |
AKAP12 | DITDDGQKE | SKIN | 133 | p.E140K | c.418G>A | Missense_Mutation | 1 | 0.11 | MEWO | N | 0 | 0 | 0 | N |
AKAP12 | DLEPQNGIL | LUNG | 1532 | p.E1536Q | c.4606G>C | Missense_Mutation | 1 | 0.11 | NCIH23 | N | 7 | 0 | 0 | N |
AKAP12 | DLSPDEMVL | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 481 | p.K487M | c.1460A>T | Missense_Mutation | 1 | 0.11 | KMS34 | N | 4 | 0 | 0 | N |
AKAP12 | DPTQGADVS | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 475 | p.L482V | c.1444C>G | Missense_Mutation | 1 | 0.11 | HT | N | 3 | 0 | 0 | N |
AKAP12 | DRSEASEKT | ENDOMETRIUM | 1633 | p.M1634R | c.4901T>G | Missense_Mutation | 1 | 0.11 | HEC6 | N | 1 | 0 | 0 | N |
AKAP12 | DSDVPAMVP | CENTRAL_NERVOUS_SYSTEM | 840 | p.V846M | c.2536G>A | Missense_Mutation | 1 | 0.11 | LN18 | N | 0 | 0 | 0 | N |
AKAP12 | DSDVPAVVL | UPPER_AERODIGESTIVE_TRACT | 840 | p.P848L | c.2543C>T | Missense_Mutation | 1 | 0.11 | HS840T | Y | 7 | 9 | 0 | N |
AKAP12 | DSEDVSERD | STOMACH | 111 | p.K117E | c.348_349CA>TG | Missense_Mutation | 1 | 0.11 | SNU1 | N | 0 | 0 | 0 | N |
AKAP12 | DSVETPTNS | LUNG | 1161 | p.D1168N | c.3502G>A | Missense_Mutation | 1 | 0.11 | HCC366 | N | 1 | 0 | 0 | N |
AKAP12 | DTEAEAVPA | ENDOMETRIUM | 1208 | p.G1208D | c.3623G>A | Missense_Mutation | 1 | 0.11 | HEC1B | N | 1 | 0 | 0 | N |
AKAP12 | DTGQGSSSP | ENDOMETRIUM | 736 | p.P737T | c.2209C>A | Missense_Mutation | 1 | 0.11 | HEC251 | N | 0 | 0 | 0 | N |
AKAP12 | DTKEDGKAE | OESOPHAGUS | 336 | p.E338K | c.1012G>A | Missense_Mutation | 1 | 0.11 | KYSE410 | N | 0 | 0 | 0 | N |
AKAP12 | DVHQEEVVA | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 409 | p.E409D | c.1227A>T | Missense_Mutation | 1 | 0.11 | WSUDLCL2 | N | 2 | 0 | 0 | N |
AKAP12 | DVPAMVPLS | CENTRAL_NERVOUS_SYSTEM | 842 | p.V846M | c.2536G>A | Missense_Mutation | 1 | 0.11 | LN18 | N | 2 | 0 | 0 | N |
AKAP12 | DVPAVVLLS | UPPER_AERODIGESTIVE_TRACT | 842 | p.P848L | c.2543C>T | Missense_Mutation | 1 | 0.11 | HS840T | N | 2 | 0 | 0 | N |
AKAP12 | DVSERDSDK | STOMACH | 114 | p.K117E | c.348_349CA>TG | Missense_Mutation | 1 | 0.11 | SNU1 | N | 4 | 0 | 0 | N |
AKAP12 | DVSPDEKVL | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 481 | p.L482V | c.1444C>G | Missense_Mutation | 1 | 0.11 | HT | N | 4 | 0 | 0 | N |
AKAP12 | EAASKESES | PROSTATE | 224 | p.P232S | c.694C>T | Missense_Mutation | 1 | 0.11 | DU145 | N | 2 | 0 | 0 | N |
AKAP12 | EAASKESKP | LARGE_INTESTINE | 224 | p.E231K | c.691G>A | Missense_Mutation | 1 | 0.11 | SNU81 | N | 0 | 0 | 0 | N |
AKAP12 | EAEKGATSD | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 591 | p.E594K | c.1780G>A | Missense_Mutation | 1 | 0.11 | MOLT13 | N | 0 | 0 | 0 | N |
AKAP12 | EAEPTYVNE | LARGE_INTESTINE | 1347 | p.H1352Y | c.4054C>T | Missense_Mutation | 1 | 0.11 | LS123 | N | 1 | 0 | 0 | N |
AKAP12 | EAQLAQKSA | LUNG | 861 | p.Q864L | c.2591A>T | Missense_Mutation | 1 | 0.11 | NCIH23 | N | 2 | 0 | 0 | N |
AKAP12 | EAQRPEEQA | LUNG | 1073 | p.E1075Q | c.3223G>C | Missense_Mutation | 1 | 0.11 | HCC78 | N | 2 | 0 | 0 | N |
AKAP12 | EDDSDVPAM | CENTRAL_NERVOUS_SYSTEM | 838 | p.V846M | c.2536G>A | Missense_Mutation | 1 | 0.11 | LN18 | N | 2 | 0 | 0 | N |
AKAP12 | EDGKAEVVS | ENDOMETRIUM | 339 | p.A346V | c.1037C>T | Missense_Mutation | 1 | 0.11 | MFE319 | N | 2 | 0 | 0 | N |
AKAP12 | EDLEPQNGI | LUNG | 1531 | p.E1536Q | c.4606G>C | Missense_Mutation | 1 | 0.11 | NCIH23 | N | 5 | 0 | 0 | N |
AKAP12 | EDPTQGADV | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 474 | p.L482V | c.1444C>G | Missense_Mutation | 1 | 0.11 | HT | N | 4 | 0 | 0 | N |
AKAP12 | EDVSERDSD | STOMACH | 113 | p.K117E | c.348_349CA>TG | Missense_Mutation | 1 | 0.11 | SNU1 | N | 0 | 0 | 0 | N |
AKAP12 | EEDGKAEVV | ENDOMETRIUM | 338 | p.A346V | c.1037C>T | Missense_Mutation | 1 | 0.11 | MFE319 | N | 7 | 0 | 0 | N |
AKAP12 | EEKLEYETA | LUNG | 1355 | p.H1360Y | c.4078C>T | Missense_Mutation | 1 | 0.11 | NCIH2286 | N | 5 | 0 | 0 | N |
AKAP12 | EEMKGSMEE | LARGE_INTESTINE | 655 | p.V661M | c.1981G>A | Missense_Mutation | 1 | 0.11 | LS411N | N | 0 | 0 | 0 | N |
AKAP12 | EESGEHTRV | STOMACH | 542 | p.Q549R | c.1646A>G | Missense_Mutation | 1 | 0.11 | 2313287 | N | 6 | 0 | 0 | N |
AKAP12 | EETTTEMLT | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 1565 | p.A1568T | c.4702G>A | Missense_Mutation | 1 | 0.11 | HT | N | 6 | 0 | 0 | N |
AKAP12 | EGVTSWASF | UPPER_AERODIGESTIVE_TRACT | 605 | p.P609S | c.1825C>T | Missense_Mutation | 1 | 0.11 | PECAPJ49 | N | 4 | 0 | 0 | N |
AKAP12 | EHDTGQGSS | ENDOMETRIUM | 734 | p.P737T | c.2209C>A | Missense_Mutation | 1 | 0.11 | HEC251 | N | 2 | 0 | 0 | N |
AKAP12 | EHEKGDDVD | LUNG | 1697 | p.D1698H | c.5092G>C | Missense_Mutation | 1 | 0.11 | NCIH23 | N | 0 | 0 | 0 | N |
AKAP12 | EHTQVPADF | ENDOMETRIUM | 546 | p.S554F | c.1661C>T | Missense_Mutation | 1 | 0.11 | JHUEM7 | N | 2 | 0 | 0 | Y |
AKAP12 | EHTRVPADS | STOMACH | 546 | p.Q549R | c.1646A>G | Missense_Mutation | 1 | 0.11 | 2313287 | N | 1 | 0 | 0 | N |
AKAP12 | EKAPQVTEN | LARGE_INTESTINE | 1121 | p.S1129N | c.3386G>A | Missense_Mutation | 1 | 0.11 | KM12 | N | 1 | 0 | 0 | N |
AKAP12 | EKGATSDGE | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 593 | p.E594K | c.1780G>A | Missense_Mutation | 1 | 0.11 | MOLT13 | N | 0 | 0 | 0 | N |
AKAP12 | EKGLDEVQQ | LUNG | 580 | p.A584D | c.1751C>A | Missense_Mutation | 1 | 0.11 | SW1271 | N | 0 | 0 | 0 | N |
AKAP12 | EKIDVHQEE | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 406 | p.E409D | c.1227A>T | Missense_Mutation | 1 | 0.11 | WSUDLCL2 | N | 0 | 0 | 0 | N |
AKAP12 | EKKREGVTS | UPPER_AERODIGESTIVE_TRACT | 601 | p.P609S | c.1825C>T | Missense_Mutation | 1 | 0.11 | PECAPJ49 | N | 1 | 0 | 0 | N |
AKAP12 | EKLEYETAV | LUNG | 1356 | p.H1360Y | c.4078C>T | Missense_Mutation | 1 | 0.11 | NCIH2286 | N | 2 | 0 | 0 | N |
AKAP12 | EKMEAQLAQ | LUNG | 858 | p.Q864L | c.2591A>T | Missense_Mutation | 1 | 0.11 | NCIH23 | N | 0 | 0 | 0 | N |
AKAP12 | EKTEAEPTY | LARGE_INTESTINE | 1344 | p.H1352Y | c.4054C>T | Missense_Mutation | 1 | 0.11 | LS123 | N | 2 | 0 | 0 | N |
AKAP12 | EKVDTKEDG | OESOPHAGUS | 333 | p.E338K | c.1012G>A | Missense_Mutation | 1 | 0.11 | KYSE410 | N | 0 | 0 | 0 | N |
AKAP12 | ELHSHAKSP | LUNG | 1321 | p.Q1323H | c.3969G>T | Missense_Mutation | 1 | 0.11 | NCIH2106 | N | 0 | 0 | 0 | N |
AKAP12 | EMATKSAVD | UPPER_AERODIGESTIVE_TRACT | 123 | p.V131D | c.392T>A | Missense_Mutation | 1 | 0.11 | SNU46 | N | 0 | 0 | 0 | N |
AKAP12 | EMEKMEAQQ | LARGE_INTESTINE | 856 | p.R857M | c.2570G>T | Missense_Mutation | 1 | 0.11 | CW2 | N | 1 | 0 | 0 | N |
AKAP12 | EMKGSMEEP | LARGE_INTESTINE | 656 | p.V661M | c.1981G>A | Missense_Mutation | 1 | 0.11 | LS411N | N | 0 | 0 | 0 | N |
AKAP12 | EMVLSKPPE | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 486 | p.K487M | c.1460A>T | Missense_Mutation | 1 | 0.11 | KMS34 | N | 0 | 0 | 0 | N |
AKAP12 | ENIESSELV | LARGE_INTESTINE | 1128 | p.S1129N | c.3386G>A | Missense_Mutation | 1 | 0.11 | KM12 | N | 2 | 0 | 0 | N |
AKAP12 | ENQNSALTD | PROSTATE | 1708 | p.A1715T | c.5143G>A | Missense_Mutation | 1 | 0.11 | 22RV1 | N | 0 | 0 | 0 | N |
AKAP12 | EPEKVDTKE | OESOPHAGUS | 331 | p.E338K | c.1012G>A | Missense_Mutation | 1 | 0.11 | KYSE410 | N | 0 | 0 | 0 | N |
AKAP12 | EPKEHEKGD | LUNG | 1694 | p.D1698H | c.5092G>C | Missense_Mutation | 1 | 0.11 | NCIH23 | N | 0 | 0 | 0 | N |
AKAP12 | EPQNGILEL | LUNG | 1534 | p.E1536Q | c.4606G>C | Missense_Mutation | 1 | 0.11 | NCIH23 | Y | 20 | 11 | 0 | Y |
AKAP12 | EPTYVNEEK | LARGE_INTESTINE | 1349 | p.H1352Y | c.4054C>T | Missense_Mutation | 1 | 0.11 | LS123 | N | 1 | 0 | 0 | N |
AKAP12 | ERDSDKEMA | STOMACH | 117 | p.K117E | c.348_349CA>TG | Missense_Mutation | 1 | 0.11 | SNU1 | N | 1 | 0 | 0 | Y |
AKAP12 | EREKMEAQL | LUNG | 856 | p.Q864L | c.2591A>T | Missense_Mutation | 1 | 0.11 | NCIH23 | N | 6 | 0 | 0 | N |
AKAP12 | ESESKQSTE | PROSTATE | 229 | p.P232S | c.694C>T | Missense_Mutation | 1 | 0.11 | DU145 | N | 0 | 0 | 0 | N |
AKAP12 | ESGEHTRVP | STOMACH | 543 | p.Q549R | c.1646A>G | Missense_Mutation | 1 | 0.11 | 2313287 | N | 0 | 0 | 0 | N |
AKAP12 | ESKPKQSTE | LARGE_INTESTINE | 229 | p.E231K | c.691G>A | Missense_Mutation | 1 | 0.11 | SNU81 | N | 1 | 0 | 0 | N |
AKAP12 | ESKQSTEKP | PROSTATE | 231 | p.P232S | c.694C>T | Missense_Mutation | 1 | 0.11 | DU145 | N | 0 | 0 | 0 | N |
AKAP12 | ESTAVGQAR | LARGE_INTESTINE | 1619 | p.H1627R | c.4880A>G | Missense_Mutation | 1 | 0.11 | CL11 | N | 3 | 0 | 0 | N |
AKAP12 | ETCVSREDP | LIVER | 468 | p.G473R | c.1417G>A | Missense_Mutation | 1 | 0.11 | SNU449 | N | 0 | 0 | 0 | N |
AKAP12 | ETPTNSETD | LUNG | 1164 | p.D1168N | c.3502G>A | Missense_Mutation | 1 | 0.11 | HCC366 | N | 1 | 0 | 0 | N |
AKAP12 | ETTTEMLTS | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 1566 | p.A1568T | c.4702G>A | Missense_Mutation | 1 | 0.11 | HT | N | 0 | 0 | 0 | N |
AKAP12 | EVFDEKIDV | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 402 | p.E409D | c.1227A>T | Missense_Mutation | 1 | 0.11 | WSUDLCL2 | N | 9 | 0 | 0 | N |
AKAP12 | EVVSEKLTA | ENDOMETRIUM | 344 | p.A346V | c.1037C>T | Missense_Mutation | 1 | 0.11 | MFE319 | N | 2 | 0 | 0 | N |
AKAP12 | EYDAVEMEK | LARGE_INTESTINE | 851 | p.R857M | c.2570G>T | Missense_Mutation | 1 | 0.11 | CW2 | N | 3 | 0 | 0 | N |
AKAP12 | EYETAVTVS | LUNG | 1359 | p.H1360Y | c.4078C>T | Missense_Mutation | 1 | 0.11 | NCIH2286 | N | 2 | 0 | 0 | N |
AKAP12 | FDEKIDVHQ | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 404 | p.E409D | c.1227A>T | Missense_Mutation | 1 | 0.11 | WSUDLCL2 | N | 2 | 0 | 0 | N |
AKAP12 | FDLEGEKTT | SKIN | 1498 | p.S1498F | c.4493C>T | Missense_Mutation | 1 | 0.11 | MEWO | N | 5 | 0 | 0 | N |
AKAP12 | FKKFSTQGW | STOMACH | 296 | p.F300S | c.899T>C | Missense_Mutation | 1 | 0.11 | SNU1 | N | 4 | 0 | 8 | N |
AKAP12 | FPDSQEEQK | ENDOMETRIUM | 554 | p.S554F | c.1661C>T | Missense_Mutation | 1 | 0.11 | JHUEM7 | N | 5 | 0 | 0 | N |
AKAP12 | FSTQGWAGW | STOMACH | 299 | p.F300S | c.899T>C | Missense_Mutation | 1 | 0.11 | SNU1 | Y | 6 | 10 | 0 | N |
AKAP12 | FVRTEETTT | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 1561 | p.A1568T | c.4702G>A | Missense_Mutation | 1 | 0.11 | HT | N | 4 | 0 | 0 | N |
AKAP12 | GADLSPDEM | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 479 | p.K487M | c.1460A>T | Missense_Mutation | 1 | 0.11 | KMS34 | N | 4 | 0 | 0 | N |
AKAP12 | GADVSPDEK | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 479 | p.L482V | c.1444C>G | Missense_Mutation | 1 | 0.11 | HT | N | 3 | 0 | 0 | N |
AKAP12 | GDTEAEAVP | ENDOMETRIUM | 1207 | p.G1208D | c.3623G>A | Missense_Mutation | 1 | 0.11 | HEC1B | N | 0 | 0 | 0 | N |
AKAP12 | GEAASKESK | LARGE_INTESTINE | 223 | p.E231K | c.691G>A | Missense_Mutation | 1 | 0.11 | SNU81 | N | 3 | 0 | 0 | N |
AKAP12 | GEAEKGATS | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 590 | p.E594K | c.1780G>A | Missense_Mutation | 1 | 0.11 | MOLT13 | N | 4 | 0 | 0 | N |
AKAP12 | GEHTRVPAD | STOMACH | 545 | p.Q549R | c.1646A>G | Missense_Mutation | 1 | 0.11 | 2313287 | N | 0 | 0 | 0 | N |
AKAP12 | GKAEVVSEK | ENDOMETRIUM | 341 | p.A346V | c.1037C>T | Missense_Mutation | 1 | 0.11 | MFE319 | Y | 1 | 14 | 0 | Y |
AKAP12 | GKIGGGDEE | ENDOMETRIUM | 535 | p.R537I | c.1610G>T | Missense_Mutation | 1 | 0.11 | HEC251 | N | 0 | 0 | 0 | N |
AKAP12 | GKKQKGKIG | ENDOMETRIUM | 530 | p.R537I | c.1610G>T | Missense_Mutation | 1 | 0.11 | HEC251 | N | 0 | 0 | 0 | N |
AKAP12 | GLDEVQQDG | LUNG | 582 | p.A584D | c.1751C>A | Missense_Mutation | 1 | 0.11 | SW1271 | N | 0 | 0 | 0 | N |
AKAP12 | GLSFDLEGE | SKIN | 1495 | p.S1498F | c.4493C>T | Missense_Mutation | 1 | 0.11 | MEWO | N | 0 | 0 | 0 | N |
AKAP12 | GQARSDISK | LARGE_INTESTINE | 1624 | p.H1627R | c.4880A>G | Missense_Mutation | 1 | 0.11 | CL11 | Y | 5 | 12 | 0 | N |
AKAP12 | GQKETPEII | SKIN | 138 | p.E140K | c.418G>A | Missense_Mutation | 1 | 0.11 | MEWO | N | 9 | 0 | 0 | N |
AKAP12 | GQLSTINSV | LARGE_INTESTINE | 60 | p.G67S | c.199G>A | Missense_Mutation | 1 | 0.11 | C2BBE1 | Y | 10 | 10 | 0 | N |
AKAP12 | GSMEEPKPE | LARGE_INTESTINE | 659 | p.V661M | c.1981G>A | Missense_Mutation | 1 | 0.11 | LS411N | N | 0 | 0 | 0 | N |
AKAP12 | GSQEHDTGQ | ENDOMETRIUM | 731 | p.P737T | c.2209C>A | Missense_Mutation | 1 | 0.11 | HEC251 | N | 0 | 0 | 0 | N |
AKAP12 | GSTFKKFST | STOMACH | 293 | p.F300S | c.899T>C | Missense_Mutation | 1 | 0.11 | SNU1 | N | 1 | 0 | 0 | N |
AKAP12 | GTQSGDTEA | ENDOMETRIUM | 1203 | p.G1208D | c.3623G>A | Missense_Mutation | 1 | 0.11 | HEC1B | N | 1 | 0 | 0 | N |
AKAP12 | GVTSWASFK | UPPER_AERODIGESTIVE_TRACT | 606 | p.P609S | c.1825C>T | Missense_Mutation | 1 | 0.11 | PECAPJ49 | N | 3 | 0 | 0 | N |
AKAP12 | HDITDDGQK | SKIN | 132 | p.E140K | c.418G>A | Missense_Mutation | 1 | 0.11 | MEWO | N | 0 | 0 | 0 | N |
AKAP12 | HDTGQGSSS | ENDOMETRIUM | 735 | p.P737T | c.2209C>A | Missense_Mutation | 1 | 0.11 | HEC251 | N | 1 | 0 | 0 | N |
AKAP12 | HEKGDDVDD | LUNG | 1698 | p.D1698H | c.5092G>C | Missense_Mutation | 1 | 0.11 | NCIH23 | N | 0 | 0 | 0 | N |
AKAP12 | HSDISKDRS | ENDOMETRIUM | 1627 | p.M1634R | c.4901T>G | Missense_Mutation | 1 | 0.11 | HEC6 | N | 1 | 0 | 0 | Y |
AKAP12 | HSHAKSPPS | LUNG | 1323 | p.Q1323H | c.3969G>T | Missense_Mutation | 1 | 0.11 | NCIH2106 | N | 1 | 0 | 0 | N |
AKAP12 | HTQVPADFP | ENDOMETRIUM | 547 | p.S554F | c.1661C>T | Missense_Mutation | 1 | 0.11 | JHUEM7 | N | 0 | 0 | 0 | Y |
AKAP12 | HTRVPADSP | STOMACH | 547 | p.Q549R | c.1646A>G | Missense_Mutation | 1 | 0.11 | 2313287 | N | 0 | 0 | 0 | N |
AKAP12 | HVIKANSQD | LUNG | 1581 | p.D1586N | c.4756G>A | Missense_Mutation | 1 | 0.11 | NCIH23 | N | 0 | 0 | 0 | N |
AKAP12 | HVNEEKLEY | LUNG | 1352 | p.H1360Y | c.4078C>T | Missense_Mutation | 1 | 0.11 | NCIH2286 | N | 4 | 0 | 0 | N |
AKAP12 | IDVHQEEVV | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 408 | p.E409D | c.1227A>T | Missense_Mutation | 1 | 0.11 | WSUDLCL2 | N | 6 | 0 | 0 | Y |
AKAP12 | IEDLEPQNG | LUNG | 1530 | p.E1536Q | c.4606G>C | Missense_Mutation | 1 | 0.11 | NCIH23 | N | 0 | 0 | 0 | N |
AKAP12 | IGGGDEESG | ENDOMETRIUM | 537 | p.R537I | c.1610G>T | Missense_Mutation | 1 | 0.11 | HEC251 | N | 0 | 0 | 0 | N |
AKAP12 | IKANSQDAG | LUNG | 1583 | p.D1586N | c.4756G>A | Missense_Mutation | 1 | 0.11 | NCIH23 | N | 0 | 0 | 0 | N |
AKAP12 | INSVAEQDE | LARGE_INTESTINE | 65 | p.G67S | c.199G>A | Missense_Mutation | 1 | 0.11 | C2BBE1 | N | 0 | 0 | 0 | N |
AKAP12 | ISKDRSEAS | ENDOMETRIUM | 1630 | p.M1634R | c.4901T>G | Missense_Mutation | 1 | 0.11 | HEC6 | N | 2 | 0 | 8 | N |
AKAP12 | ITCLEKGLD | LUNG | 576 | p.A584D | c.1751C>A | Missense_Mutation | 1 | 0.11 | SW1271 | N | 0 | 0 | 1 | N |
AKAP12 | ITDDGQKET | SKIN | 134 | p.E140K | c.418G>A | Missense_Mutation | 1 | 0.11 | MEWO | N | 2 | 0 | 0 | N |
AKAP12 | KAEVVSEKL | ENDOMETRIUM | 342 | p.A346V | c.1037C>T | Missense_Mutation | 1 | 0.11 | MFE319 | N | 12 | 0 | 0 | N |
AKAP12 | KANSQDAGQ | LUNG | 1584 | p.D1586N | c.4756G>A | Missense_Mutation | 1 | 0.11 | NCIH23 | N | 0 | 0 | 0 | N |
AKAP12 | KAPQVTENI | LARGE_INTESTINE | 1122 | p.S1129N | c.3386G>A | Missense_Mutation | 1 | 0.11 | KM12 | Y | 11 | 10 | 0 | Y |
AKAP12 | KDDALELHS | LUNG | 1316 | p.Q1323H | c.3969G>T | Missense_Mutation | 1 | 0.11 | NCIH2106 | N | 1 | 0 | 0 | N |
AKAP12 | KDRSEASEK | ENDOMETRIUM | 1632 | p.M1634R | c.4901T>G | Missense_Mutation | 1 | 0.11 | HEC6 | N | 0 | 0 | 0 | N |
AKAP12 | KEDGKAEVA | OESOPHAGUS | 338 | p.E338K | c.1012G>A | Missense_Mutation | 1 | 0.11 | KYSE410 | N | 6 | 0 | 0 | N |
AKAP12 | KEHEKGDDV | LUNG | 1696 | p.D1698H | c.5092G>C | Missense_Mutation | 1 | 0.11 | NCIH23 | N | 11 | 0 | 0 | N |
AKAP12 | KESESKQST | PROSTATE | 228 | p.P232S | c.694C>T | Missense_Mutation | 1 | 0.11 | DU145 | N | 5 | 0 | 0 | N |
AKAP12 | KESKPKQST | LARGE_INTESTINE | 228 | p.E231K | c.691G>A | Missense_Mutation | 1 | 0.11 | SNU81 | N | 5 | 0 | 0 | N |
AKAP12 | KETCVSRED | LIVER | 467 | p.G473R | c.1417G>A | Missense_Mutation | 1 | 0.11 | SNU449 | N | 0 | 0 | 0 | N |
AKAP12 | KETPEIIEQ | SKIN | 140 | p.E140K | c.418G>A | Missense_Mutation | 1 | 0.11 | MEWO | N | 1 | 0 | 0 | N |
AKAP12 | KFSTQGWAG | STOMACH | 298 | p.F300S | c.899T>C | Missense_Mutation | 1 | 0.11 | SNU1 | N | 0 | 0 | 0 | N |
AKAP12 | KGATSDGEK | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 594 | p.E594K | c.1780G>A | Missense_Mutation | 1 | 0.11 | MOLT13 | N | 0 | 0 | 0 | N |
AKAP12 | KGKIGGGDE | ENDOMETRIUM | 534 | p.R537I | c.1610G>T | Missense_Mutation | 1 | 0.11 | HEC251 | N | 0 | 0 | 0 | N |
AKAP12 | KGLDEVQQD | LUNG | 581 | p.A584D | c.1751C>A | Missense_Mutation | 1 | 0.11 | SW1271 | N | 0 | 0 | 0 | N |
AKAP12 | KGLSFDLEG | SKIN | 1494 | p.S1498F | c.4493C>T | Missense_Mutation | 1 | 0.11 | MEWO | N | 0 | 0 | 0 | N |
AKAP12 | KGSMEEPKP | LARGE_INTESTINE | 658 | p.V661M | c.1981G>A | Missense_Mutation | 1 | 0.11 | LS411N | N | 0 | 0 | 0 | N |
AKAP12 | KGVVSEVEM | BREAST | 494 | p.E494K | c.1480G>A | Missense_Mutation | 1 | 0.11 | CAL148 | N | 7 | 0 | 0 | N |
AKAP12 | KIDVHQEEV | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 407 | p.E409D | c.1227A>T | Missense_Mutation | 1 | 0.11 | WSUDLCL2 | N | 4 | 0 | 0 | N |
AKAP12 | KIGGGDEES | ENDOMETRIUM | 536 | p.R537I | c.1610G>T | Missense_Mutation | 1 | 0.11 | HEC251 | N | 0 | 0 | 0 | N |
AKAP12 | KKDDALELH | LUNG | 1315 | p.Q1323H | c.3969G>T | Missense_Mutation | 1 | 0.11 | NCIH2106 | N | 1 | 0 | 0 | Y |
AKAP12 | KKFSTQGWA | STOMACH | 297 | p.F300S | c.899T>C | Missense_Mutation | 1 | 0.11 | SNU1 | N | 6 | 0 | 0 | N |
AKAP12 | KKGLSFDLE | SKIN | 1493 | p.S1498F | c.4493C>T | Missense_Mutation | 1 | 0.11 | MEWO | N | 0 | 0 | 0 | N |
AKAP12 | KKQKGKIGG | ENDOMETRIUM | 531 | p.R537I | c.1610G>T | Missense_Mutation | 1 | 0.11 | HEC251 | N | 0 | 0 | 0 | N |
AKAP12 | KKRARRWSS | ENDOMETRIUM | 689 | p.G695W | c.2083G>T | Missense_Mutation | 1 | 0.11 | SNGM | N | 2 | 0 | 0 | N |
AKAP12 | KKREGVTSW | UPPER_AERODIGESTIVE_TRACT | 602 | p.P609S | c.1825C>T | Missense_Mutation | 1 | 0.11 | PECAPJ49 | N | 3 | 0 | 0 | N |
AKAP12 | KLEYETAVT | LUNG | 1357 | p.H1360Y | c.4078C>T | Missense_Mutation | 1 | 0.11 | NCIH2286 | N | 1 | 0 | 0 | N |
AKAP12 | KLKETCVSR | LIVER | 465 | p.G473R | c.1417G>A | Missense_Mutation | 1 | 0.11 | SNU449 | Y | 7 | 10 | 0 | N |
AKAP12 | KMEAQLAQK | LUNG | 859 | p.Q864L | c.2591A>T | Missense_Mutation | 1 | 0.11 | NCIH23 | N | 6 | 0 | 0 | N |
AKAP12 | KPKQSTEKP | LARGE_INTESTINE | 231 | p.E231K | c.691G>A | Missense_Mutation | 1 | 0.11 | SNU81 | N | 1 | 0 | 0 | N |
AKAP12 | KPPKGVVSE | BREAST | 491 | p.E494K | c.1480G>A | Missense_Mutation | 1 | 0.11 | CAL148 | N | 1 | 0 | 0 | N |
AKAP12 | KQKGKIGGG | ENDOMETRIUM | 532 | p.R537I | c.1610G>T | Missense_Mutation | 1 | 0.11 | HEC251 | N | 1 | 0 | 0 | N |
AKAP12 | KRARRWSSS | ENDOMETRIUM | 690 | p.G695W | c.2083G>T | Missense_Mutation | 1 | 0.11 | SNGM | N | 3 | 0 | 0 | N |
AKAP12 | KREGVTSWA | UPPER_AERODIGESTIVE_TRACT | 603 | p.P609S | c.1825C>T | Missense_Mutation | 1 | 0.11 | PECAPJ49 | Y | 2 | 9 | 0 | N |
AKAP12 | KSAVDHDIT | UPPER_AERODIGESTIVE_TRACT | 127 | p.V131D | c.392T>A | Missense_Mutation | 1 | 0.11 | SNU46 | N | 1 | 0 | 0 | N |
AKAP12 | KSLVEPKEH | LUNG | 1690 | p.D1698H | c.5092G>C | Missense_Mutation | 1 | 0.11 | NCIH23 | N | 0 | 0 | 0 | N |
AKAP12 | KTEAEPTYV | LARGE_INTESTINE | 1345 | p.H1352Y | c.4054C>T | Missense_Mutation | 1 | 0.11 | LS123 | Y | 2 | 14 | 0 | N |
AKAP12 | KVDTKEDGK | OESOPHAGUS | 334 | p.E338K | c.1012G>A | Missense_Mutation | 1 | 0.11 | KYSE410 | N | 6 | 0 | 0 | N |
AKAP12 | KVLSKPPKG | BREAST | 487 | p.E494K | c.1480G>A | Missense_Mutation | 1 | 0.11 | CAL148 | N | 0 | 0 | 0 | N |
AKAP12 | LAGSQEHDT | ENDOMETRIUM | 729 | p.P737T | c.2209C>A | Missense_Mutation | 1 | 0.11 | HEC251 | N | 2 | 0 | 0 | N |
AKAP12 | LAQKSAEQP | LUNG | 864 | p.Q864L | c.2591A>T | Missense_Mutation | 1 | 0.11 | NCIH23 | N | 0 | 0 | 0 | N |
AKAP12 | LDEVQQDGE | LUNG | 583 | p.A584D | c.1751C>A | Missense_Mutation | 1 | 0.11 | SW1271 | N | 0 | 0 | 0 | N |
AKAP12 | LEKGLDEVQ | LUNG | 579 | p.A584D | c.1751C>A | Missense_Mutation | 1 | 0.11 | SW1271 | N | 0 | 0 | 0 | N |
AKAP12 | LELHSHAKS | LUNG | 1320 | p.Q1323H | c.3969G>T | Missense_Mutation | 1 | 0.11 | NCIH2106 | N | 4 | 0 | 11 | N |
AKAP12 | LEPQNGILE | LUNG | 1533 | p.E1536Q | c.4606G>C | Missense_Mutation | 1 | 0.11 | NCIH23 | N | 0 | 0 | 0 | N |
AKAP12 | LEYETAVTV | LUNG | 1358 | p.H1360Y | c.4078C>T | Missense_Mutation | 1 | 0.11 | NCIH2286 | Y | 15 | 12 | 2 | N |
AKAP12 | LHSHAKSPP | LUNG | 1322 | p.Q1323H | c.3969G>T | Missense_Mutation | 1 | 0.11 | NCIH2106 | N | 0 | 0 | 3 | N |
AKAP12 | LKETCVSRE | LIVER | 466 | p.G473R | c.1417G>A | Missense_Mutation | 1 | 0.11 | SNU449 | N | 0 | 0 | 0 | N |
AKAP12 | LLSEYDAVE | UPPER_AERODIGESTIVE_TRACT | 848 | p.P848L | c.2543C>T | Missense_Mutation | 1 | 0.11 | HS840T | N | 1 | 0 | 0 | N |
AKAP12 | LSEYDAVEM | LARGE_INTESTINE | 849 | p.R857M | c.2570G>T | Missense_Mutation | 1 | 0.11 | CW2 | N | 4 | 0 | 0 | N |
AKAP12 | LSFDLEGEK | SKIN | 1496 | p.S1498F | c.4493C>T | Missense_Mutation | 1 | 0.11 | MEWO | N | 2 | 0 | 0 | N |
AKAP12 | LSKPPKGVV | BREAST | 489 | p.E494K | c.1480G>A | Missense_Mutation | 1 | 0.11 | CAL148 | N | 6 | 0 | 0 | N |
AKAP12 | LSPDEMVLS | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 482 | p.K487M | c.1460A>T | Missense_Mutation | 1 | 0.11 | KMS34 | N | 1 | 0 | 5 | N |
AKAP12 | LSTINSVAE | LARGE_INTESTINE | 62 | p.G67S | c.199G>A | Missense_Mutation | 1 | 0.11 | C2BBE1 | N | 0 | 0 | 2 | N |
AKAP12 | LTDTDASGG | PROSTATE | 1714 | p.A1715T | c.5143G>A | Missense_Mutation | 1 | 0.11 | 22RV1 | N | 1 | 0 | 0 | N |
AKAP12 | LVEPKEHEK | LUNG | 1692 | p.D1698H | c.5092G>C | Missense_Mutation | 1 | 0.11 | NCIH23 | N | 4 | 0 | 0 | N |
AKAP12 | MATKSAVDH | UPPER_AERODIGESTIVE_TRACT | 124 | p.V131D | c.392T>A | Missense_Mutation | 1 | 0.11 | SNU46 | N | 0 | 0 | 1 | N |
AKAP12 | MEAQLAQKS | LUNG | 860 | p.Q864L | c.2591A>T | Missense_Mutation | 1 | 0.11 | NCIH23 | N | 4 | 0 | 0 | N |
AKAP12 | MEEPKPEEP | LARGE_INTESTINE | 661 | p.V661M | c.1981G>A | Missense_Mutation | 1 | 0.11 | LS411N | N | 0 | 0 | 0 | N |
AKAP12 | MEKMEAQQA | LARGE_INTESTINE | 857 | p.R857M | c.2570G>T | Missense_Mutation | 1 | 0.11 | CW2 | N | 6 | 0 | 3 | N |
AKAP12 | MKGSMEEPK | LARGE_INTESTINE | 657 | p.V661M | c.1981G>A | Missense_Mutation | 1 | 0.11 | LS411N | N | 1 | 0 | 0 | N |
AKAP12 | MQEEMKGSM | LARGE_INTESTINE | 653 | p.V661M | c.1981G>A | Missense_Mutation | 1 | 0.11 | LS411N | N | 5 | 0 | 0 | N |
AKAP12 | MVLSKPPEG | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 487 | p.K487M | c.1460A>T | Missense_Mutation | 1 | 0.11 | KMS34 | N | 0 | 0 | 17 | N |
AKAP12 | MVPLSEYDA | CENTRAL_NERVOUS_SYSTEM | 846 | p.V846M | c.2536G>A | Missense_Mutation | 1 | 0.11 | LN18 | N | 4 | 0 | 2 | N |
AKAP12 | NEEKLEYET | LUNG | 1354 | p.H1360Y | c.4078C>T | Missense_Mutation | 1 | 0.11 | NCIH2286 | N | 5 | 0 | 0 | N |
AKAP12 | NGQLSTINS | LARGE_INTESTINE | 59 | p.G67S | c.199G>A | Missense_Mutation | 1 | 0.11 | C2BBE1 | N | 1 | 0 | 0 | Y |
AKAP12 | NIESSELVT | LARGE_INTESTINE | 1129 | p.S1129N | c.3386G>A | Missense_Mutation | 1 | 0.11 | KM12 | N | 1 | 0 | 0 | N |
AKAP12 | NQNSALTDT | PROSTATE | 1709 | p.A1715T | c.5143G>A | Missense_Mutation | 1 | 0.11 | 22RV1 | N | 2 | 0 | 0 | N |
AKAP12 | NSALTDTDA | PROSTATE | 1711 | p.A1715T | c.5143G>A | Missense_Mutation | 1 | 0.11 | 22RV1 | N | 1 | 0 | 0 | N |
AKAP12 | NSETDGSTP | LUNG | 1168 | p.D1168N | c.3502G>A | Missense_Mutation | 1 | 0.11 | HCC366 | N | 0 | 0 | 0 | N |
AKAP12 | NSQDAGQET | LUNG | 1586 | p.D1586N | c.4756G>A | Missense_Mutation | 1 | 0.11 | NCIH23 | N | 1 | 0 | 0 | N |
AKAP12 | NSVAEQDEL | LARGE_INTESTINE | 66 | p.G67S | c.199G>A | Missense_Mutation | 1 | 0.11 | C2BBE1 | Y | 12 | 9 | 0 | N |
AKAP12 | PADFPDSQE | ENDOMETRIUM | 551 | p.S554F | c.1661C>T | Missense_Mutation | 1 | 0.11 | JHUEM7 | N | 0 | 0 | 0 | N |
AKAP12 | PAMVPLSEY | CENTRAL_NERVOUS_SYSTEM | 844 | p.V846M | c.2536G>A | Missense_Mutation | 1 | 0.11 | LN18 | N | 0 | 0 | 0 | N |
AKAP12 | PAVVLLSEY | UPPER_AERODIGESTIVE_TRACT | 844 | p.P848L | c.2543C>T | Missense_Mutation | 1 | 0.11 | HS840T | N | 0 | 0 | 0 | N |
AKAP12 | PDEMVLSKP | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 484 | p.K487M | c.1460A>T | Missense_Mutation | 1 | 0.11 | KMS34 | N | 0 | 0 | 0 | N |
AKAP12 | PDSVETPTN | LUNG | 1160 | p.D1168N | c.3502G>A | Missense_Mutation | 1 | 0.11 | HCC366 | N | 0 | 0 | 0 | N |
AKAP12 | PEKVDTKED | OESOPHAGUS | 332 | p.E338K | c.1012G>A | Missense_Mutation | 1 | 0.11 | KYSE410 | N | 0 | 0 | 0 | N |
AKAP12 | PENQNSALT | PROSTATE | 1707 | p.A1715T | c.5143G>A | Missense_Mutation | 1 | 0.11 | 22RV1 | N | 0 | 0 | 0 | N |
AKAP12 | PKEHEKGDD | LUNG | 1695 | p.D1698H | c.5092G>C | Missense_Mutation | 1 | 0.11 | NCIH23 | N | 0 | 0 | 0 | N |
AKAP12 | PKGVVSEVE | BREAST | 493 | p.E494K | c.1480G>A | Missense_Mutation | 1 | 0.11 | CAL148 | N | 0 | 0 | 0 | N |
AKAP12 | PPKGVVSEV | BREAST | 492 | p.E494K | c.1480G>A | Missense_Mutation | 1 | 0.11 | CAL148 | N | 7 | 0 | 0 | N |
AKAP12 | PQNGILELE | LUNG | 1535 | p.E1536Q | c.4606G>C | Missense_Mutation | 1 | 0.11 | NCIH23 | N | 0 | 0 | 0 | N |
AKAP12 | PQVTENIES | LARGE_INTESTINE | 1124 | p.S1129N | c.3386G>A | Missense_Mutation | 1 | 0.11 | KM12 | N | 0 | 0 | 0 | Y |
AKAP12 | PTNSETDGS | LUNG | 1166 | p.D1168N | c.3502G>A | Missense_Mutation | 1 | 0.11 | HCC366 | N | 0 | 0 | 0 | N |
AKAP12 | PTQGADVSP | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 476 | p.L482V | c.1444C>G | Missense_Mutation | 1 | 0.11 | HT | N | 0 | 0 | 0 | N |
AKAP12 | PTYVNEEKL | LARGE_INTESTINE | 1350 | p.H1352Y | c.4054C>T | Missense_Mutation | 1 | 0.11 | LS123 | N | 2 | 0 | 0 | Y |
AKAP12 | PVQRAEAQR | LUNG | 1068 | p.E1075Q | c.3223G>C | Missense_Mutation | 1 | 0.11 | HCC78 | N | 2 | 0 | 0 | N |
AKAP12 | QAHVIKANS | LUNG | 1579 | p.D1586N | c.4756G>A | Missense_Mutation | 1 | 0.11 | NCIH23 | N | 1 | 0 | 0 | N |
AKAP12 | QARSDISKD | LARGE_INTESTINE | 1625 | p.H1627R | c.4880A>G | Missense_Mutation | 1 | 0.11 | CL11 | N | 0 | 0 | 0 | N |
AKAP12 | QDGEAEKGA | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 588 | p.E594K | c.1780G>A | Missense_Mutation | 1 | 0.11 | MOLT13 | N | 3 | 0 | 0 | N |
AKAP12 | QEEMKGSME | LARGE_INTESTINE | 654 | p.V661M | c.1981G>A | Missense_Mutation | 1 | 0.11 | LS411N | N | 0 | 0 | 0 | N |
AKAP12 | QEHDTGQGS | ENDOMETRIUM | 733 | p.P737T | c.2209C>A | Missense_Mutation | 1 | 0.11 | HEC251 | N | 3 | 0 | 0 | N |
AKAP12 | QEPEKVDTK | OESOPHAGUS | 330 | p.E338K | c.1012G>A | Missense_Mutation | 1 | 0.11 | KYSE410 | N | 2 | 0 | 0 | N |
AKAP12 | QFVRTEETT | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 1560 | p.A1568T | c.4702G>A | Missense_Mutation | 1 | 0.11 | HT | N | 1 | 0 | 0 | N |
AKAP12 | QGADVSPDE | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 478 | p.L482V | c.1444C>G | Missense_Mutation | 1 | 0.11 | HT | N | 0 | 0 | 0 | N |
AKAP12 | QKETPEIIE | SKIN | 139 | p.E140K | c.418G>A | Missense_Mutation | 1 | 0.11 | MEWO | N | 0 | 0 | 0 | N |
AKAP12 | QKGKIGGGD | ENDOMETRIUM | 533 | p.R537I | c.1610G>T | Missense_Mutation | 1 | 0.11 | HEC251 | N | 0 | 0 | 0 | N |
AKAP12 | QLAQKSAEQ | LUNG | 863 | p.Q864L | c.2591A>T | Missense_Mutation | 1 | 0.11 | NCIH23 | N | 0 | 0 | 0 | N |
AKAP12 | QLSTINSVA | LARGE_INTESTINE | 61 | p.G67S | c.199G>A | Missense_Mutation | 1 | 0.11 | C2BBE1 | N | 1 | 0 | 0 | N |
AKAP12 | QNGILELET | LUNG | 1536 | p.E1536Q | c.4606G>C | Missense_Mutation | 1 | 0.11 | NCIH23 | N | 0 | 0 | 0 | N |
AKAP12 | QNSALTDTD | PROSTATE | 1710 | p.A1715T | c.5143G>A | Missense_Mutation | 1 | 0.11 | 22RV1 | N | 0 | 0 | 0 | N |
AKAP12 | QPVQRAEAQ | LUNG | 1067 | p.E1075Q | c.3223G>C | Missense_Mutation | 1 | 0.11 | HCC78 | N | 0 | 0 | 0 | N |
AKAP12 | QQDGEAEKG | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 587 | p.E594K | c.1780G>A | Missense_Mutation | 1 | 0.11 | MOLT13 | N | 0 | 0 | 0 | N |
AKAP12 | QRAEAQRPE | LUNG | 1070 | p.E1075Q | c.3223G>C | Missense_Mutation | 1 | 0.11 | HCC78 | N | 0 | 0 | 0 | N |
AKAP12 | QRDSEDVSE | STOMACH | 109 | p.K117E | c.348_349CA>TG | Missense_Mutation | 1 | 0.11 | SNU1 | N | 1 | 0 | 0 | N |
AKAP12 | QRPEEQAEA | LUNG | 1075 | p.E1075Q | c.3223G>C | Missense_Mutation | 1 | 0.11 | HCC78 | N | 3 | 0 | 0 | N |
AKAP12 | QSGDTEAEA | ENDOMETRIUM | 1205 | p.G1208D | c.3623G>A | Missense_Mutation | 1 | 0.11 | HEC1B | N | 1 | 0 | 0 | N |
AKAP12 | QVPADFPDS | ENDOMETRIUM | 549 | p.S554F | c.1661C>T | Missense_Mutation | 1 | 0.11 | JHUEM7 | N | 1 | 0 | 0 | Y |
AKAP12 | QVTENIESS | LARGE_INTESTINE | 1125 | p.S1129N | c.3386G>A | Missense_Mutation | 1 | 0.11 | KM12 | N | 1 | 0 | 0 | Y |
AKAP12 | RAEAQRPEE | LUNG | 1071 | p.E1075Q | c.3223G>C | Missense_Mutation | 1 | 0.11 | HCC78 | N | 0 | 0 | 0 | N |
AKAP12 | RARRWSSSD | ENDOMETRIUM | 691 | p.G695W | c.2083G>T | Missense_Mutation | 1 | 0.11 | SNGM | N | 0 | 0 | 0 | N |
AKAP12 | RDSEDVSER | STOMACH | 110 | p.K117E | c.348_349CA>TG | Missense_Mutation | 1 | 0.11 | SNU1 | N | 0 | 0 | 0 | N |
AKAP12 | REDPTQGAD | LIVER | 473 | p.G473R | c.1417G>A | Missense_Mutation | 1 | 0.11 | SNU449 | N | 0 | 0 | 0 | N |
AKAP12 | REGVTSWAS | UPPER_AERODIGESTIVE_TRACT | 604 | p.P609S | c.1825C>T | Missense_Mutation | 1 | 0.11 | PECAPJ49 | N | 3 | 0 | 0 | N |
AKAP12 | REKMEAQLA | LUNG | 857 | p.Q864L | c.2591A>T | Missense_Mutation | 1 | 0.11 | NCIH23 | N | 7 | 0 | 0 | N |
AKAP12 | RRWSSSDEE | ENDOMETRIUM | 693 | p.G695W | c.2083G>T | Missense_Mutation | 1 | 0.11 | SNGM | N | 2 | 0 | 0 | N |
AKAP12 | RSDISKDMS | LARGE_INTESTINE | 1627 | p.H1627R | c.4880A>G | Missense_Mutation | 1 | 0.11 | CL11 | N | 2 | 0 | 0 | N |
AKAP12 | RSEASEKTM | ENDOMETRIUM | 1634 | p.M1634R | c.4901T>G | Missense_Mutation | 1 | 0.11 | HEC6 | N | 4 | 0 | 0 | N |
AKAP12 | RTEETTTEM | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 1563 | p.A1568T | c.4702G>A | Missense_Mutation | 1 | 0.11 | HT | Y | 3 | 11 | 0 | N |
AKAP12 | RVPADSPDS | STOMACH | 549 | p.Q549R | c.1646A>G | Missense_Mutation | 1 | 0.11 | 2313287 | N | 0 | 0 | 0 | N |
AKAP12 | RWSSSDEEG | ENDOMETRIUM | 694 | p.G695W | c.2083G>T | Missense_Mutation | 1 | 0.11 | SNGM | N | 0 | 0 | 0 | N |
AKAP12 | SALTDTDAS | PROSTATE | 1712 | p.A1715T | c.5143G>A | Missense_Mutation | 1 | 0.11 | 22RV1 | N | 2 | 0 | 0 | N |
AKAP12 | SAVDHDITD | UPPER_AERODIGESTIVE_TRACT | 128 | p.V131D | c.392T>A | Missense_Mutation | 1 | 0.11 | SNU46 | N | 0 | 0 | 0 | N |
AKAP12 | SDISKDRSE | ENDOMETRIUM | 1628 | p.M1634R | c.4901T>G | Missense_Mutation | 1 | 0.11 | HEC6 | N | 0 | 0 | 0 | N |
AKAP12 | SDVPAMVPL | CENTRAL_NERVOUS_SYSTEM | 841 | p.V846M | c.2536G>A | Missense_Mutation | 1 | 0.11 | LN18 | N | 8 | 0 | 0 | N |
AKAP12 | SDVPAVVLL | UPPER_AERODIGESTIVE_TRACT | 841 | p.P848L | c.2543C>T | Missense_Mutation | 1 | 0.11 | HS840T | N | 7 | 0 | 0 | N |
AKAP12 | SEDVSERDS | STOMACH | 112 | p.K117E | c.348_349CA>TG | Missense_Mutation | 1 | 0.11 | SNU1 | N | 3 | 0 | 0 | N |
AKAP12 | SERDSDKEM | STOMACH | 116 | p.K117E | c.348_349CA>TG | Missense_Mutation | 1 | 0.11 | SNU1 | Y | 6 | 9 | 0 | N |
AKAP12 | SESKQSTEK | PROSTATE | 230 | p.P232S | c.694C>T | Missense_Mutation | 1 | 0.11 | DU145 | N | 1 | 0 | 0 | N |
AKAP12 | SEYDAVEME | LARGE_INTESTINE | 850 | p.R857M | c.2570G>T | Missense_Mutation | 1 | 0.11 | CW2 | N | 1 | 0 | 0 | N |
AKAP12 | SFDLEGEKT | SKIN | 1497 | p.S1498F | c.4493C>T | Missense_Mutation | 1 | 0.11 | MEWO | N | 1 | 0 | 0 | N |
AKAP12 | SGDTEAEAV | ENDOMETRIUM | 1206 | p.G1208D | c.3623G>A | Missense_Mutation | 1 | 0.11 | HEC1B | N | 5 | 0 | 0 | N |
AKAP12 | SGEHTRVPA | STOMACH | 544 | p.Q549R | c.1646A>G | Missense_Mutation | 1 | 0.11 | 2313287 | N | 1 | 0 | 0 | N |
AKAP12 | SGKKQKGKI | ENDOMETRIUM | 529 | p.R537I | c.1610G>T | Missense_Mutation | 1 | 0.11 | HEC251 | N | 6 | 0 | 0 | N |
AKAP12 | SGTQSGDTE | ENDOMETRIUM | 1202 | p.G1208D | c.3623G>A | Missense_Mutation | 1 | 0.11 | HEC1B | N | 0 | 0 | 0 | N |
AKAP12 | SKDRSEASE | ENDOMETRIUM | 1631 | p.M1634R | c.4901T>G | Missense_Mutation | 1 | 0.11 | HEC6 | N | 0 | 0 | 0 | N |
AKAP12 | SKESESKQS | PROSTATE | 227 | p.P232S | c.694C>T | Missense_Mutation | 1 | 0.11 | DU145 | N | 1 | 0 | 0 | N |
AKAP12 | SKESKPKQS | LARGE_INTESTINE | 227 | p.E231K | c.691G>A | Missense_Mutation | 1 | 0.11 | SNU81 | N | 1 | 0 | 0 | N |
AKAP12 | SKKRARRWS | ENDOMETRIUM | 688 | p.G695W | c.2083G>T | Missense_Mutation | 1 | 0.11 | SNGM | N | 1 | 0 | 0 | N |
AKAP12 | SKPKQSTEK | LARGE_INTESTINE | 230 | p.E231K | c.691G>A | Missense_Mutation | 1 | 0.11 | SNU81 | N | 1 | 0 | 0 | N |
AKAP12 | SKPPKGVVS | BREAST | 490 | p.E494K | c.1480G>A | Missense_Mutation | 1 | 0.11 | CAL148 | N | 2 | 0 | 0 | N |
AKAP12 | SKQSTEKPE | PROSTATE | 232 | p.P232S | c.694C>T | Missense_Mutation | 1 | 0.11 | DU145 | N | 0 | 0 | 0 | N |
AKAP12 | SLVEPKEHE | LUNG | 1691 | p.D1698H | c.5092G>C | Missense_Mutation | 1 | 0.11 | NCIH23 | N | 0 | 0 | 0 | N |
AKAP12 | SMEEPKPEE | LARGE_INTESTINE | 660 | p.V661M | c.1981G>A | Missense_Mutation | 1 | 0.11 | LS411N | N | 0 | 0 | 0 | N |
AKAP12 | SPDEMVLSK | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 483 | p.K487M | c.1460A>T | Missense_Mutation | 1 | 0.11 | KMS34 | N | 3 | 0 | 0 | N |
AKAP12 | SQEHDTGQG | ENDOMETRIUM | 732 | p.P737T | c.2209C>A | Missense_Mutation | 1 | 0.11 | HEC251 | N | 0 | 0 | 0 | N |
AKAP12 | SREDPTQGA | LIVER | 472 | p.G473R | c.1417G>A | Missense_Mutation | 1 | 0.11 | SNU449 | N | 2 | 0 | 0 | N |
AKAP12 | SSKKRARRW | ENDOMETRIUM | 687 | p.G695W | c.2083G>T | Missense_Mutation | 1 | 0.11 | SNGM | Y | 4 | 9 | 0 | Y |
AKAP12 | STAVGQARS | LARGE_INTESTINE | 1620 | p.H1627R | c.4880A>G | Missense_Mutation | 1 | 0.11 | CL11 | N | 0 | 0 | 0 | N |
AKAP12 | STFKKFSTQ | STOMACH | 294 | p.F300S | c.899T>C | Missense_Mutation | 1 | 0.11 | SNU1 | N | 0 | 0 | 0 | N |
AKAP12 | STINSVAEQ | LARGE_INTESTINE | 63 | p.G67S | c.199G>A | Missense_Mutation | 1 | 0.11 | C2BBE1 | N | 0 | 0 | 0 | N |
AKAP12 | STQGWAGWR | STOMACH | 300 | p.F300S | c.899T>C | Missense_Mutation | 1 | 0.11 | SNU1 | N | 4 | 0 | 0 | N |
AKAP12 | SVAEQDELS | LARGE_INTESTINE | 67 | p.G67S | c.199G>A | Missense_Mutation | 1 | 0.11 | C2BBE1 | N | 0 | 0 | 0 | N |
AKAP12 | SVETPTNSE | LUNG | 1162 | p.D1168N | c.3502G>A | Missense_Mutation | 1 | 0.11 | HCC366 | N | 0 | 0 | 0 | N |
AKAP12 | SWASFKKMV | UPPER_AERODIGESTIVE_TRACT | 609 | p.P609S | c.1825C>T | Missense_Mutation | 1 | 0.11 | PECAPJ49 | N | 3 | 0 | 0 | N |
AKAP12 | TAVGQARSD | LARGE_INTESTINE | 1621 | p.H1627R | c.4880A>G | Missense_Mutation | 1 | 0.11 | CL11 | N | 0 | 0 | 0 | N |
AKAP12 | TCLEKGLDE | LUNG | 577 | p.A584D | c.1751C>A | Missense_Mutation | 1 | 0.11 | SW1271 | N | 0 | 0 | 0 | N |
AKAP12 | TCVSREDPT | LIVER | 469 | p.G473R | c.1417G>A | Missense_Mutation | 1 | 0.11 | SNU449 | N | 1 | 0 | 0 | N |
AKAP12 | TDDGQKETP | SKIN | 135 | p.E140K | c.418G>A | Missense_Mutation | 1 | 0.11 | MEWO | N | 0 | 0 | 0 | N |
AKAP12 | TDTDASGGL | PROSTATE | 1715 | p.A1715T | c.5143G>A | Missense_Mutation | 1 | 0.11 | 22RV1 | N | 4 | 0 | 0 | N |
AKAP12 | TEAEPTYVN | LARGE_INTESTINE | 1346 | p.H1352Y | c.4054C>T | Missense_Mutation | 1 | 0.11 | LS123 | N | 5 | 0 | 0 | N |
AKAP12 | TEETTTEML | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 1564 | p.A1568T | c.4702G>A | Missense_Mutation | 1 | 0.11 | HT | N | 7 | 0 | 0 | N |
AKAP12 | TENIESSEL | LARGE_INTESTINE | 1127 | p.S1129N | c.3386G>A | Missense_Mutation | 1 | 0.11 | KM12 | Y | 7 | 10 | 0 | Y |
AKAP12 | TEVFDEKID | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 401 | p.E409D | c.1227A>T | Missense_Mutation | 1 | 0.11 | WSUDLCL2 | N | 1 | 0 | 0 | N |
AKAP12 | TFKKFSTQG | STOMACH | 295 | p.F300S | c.899T>C | Missense_Mutation | 1 | 0.11 | SNU1 | N | 0 | 0 | 0 | N |
AKAP12 | TGQGSSSPE | ENDOMETRIUM | 737 | p.P737T | c.2209C>A | Missense_Mutation | 1 | 0.11 | HEC251 | N | 0 | 0 | 0 | N |
AKAP12 | TGSTFKKFS | STOMACH | 292 | p.F300S | c.899T>C | Missense_Mutation | 1 | 0.11 | SNU1 | N | 0 | 0 | 0 | N |
AKAP12 | TINSVAEQD | LARGE_INTESTINE | 64 | p.G67S | c.199G>A | Missense_Mutation | 1 | 0.11 | C2BBE1 | N | 0 | 0 | 0 | N |
AKAP12 | TKEDGKAEV | OESOPHAGUS | 337 | p.E338K | c.1012G>A | Missense_Mutation | 1 | 0.11 | KYSE410 | N | 1 | 0 | 0 | N |
AKAP12 | TKKGLSFDL | SKIN | 1492 | p.S1498F | c.4493C>T | Missense_Mutation | 1 | 0.11 | MEWO | N | 3 | 0 | 0 | N |
AKAP12 | TKSAVDHDI | UPPER_AERODIGESTIVE_TRACT | 126 | p.V131D | c.392T>A | Missense_Mutation | 1 | 0.11 | SNU46 | N | 2 | 0 | 0 | N |
AKAP12 | TNSETDGST | LUNG | 1167 | p.D1168N | c.3502G>A | Missense_Mutation | 1 | 0.11 | HCC366 | N | 0 | 0 | 0 | N |
AKAP12 | TPTNSETDG | LUNG | 1165 | p.D1168N | c.3502G>A | Missense_Mutation | 1 | 0.11 | HCC366 | N | 0 | 0 | 0 | Y |
AKAP12 | TQAHVIKAN | LUNG | 1578 | p.D1586N | c.4756G>A | Missense_Mutation | 1 | 0.11 | NCIH23 | N | 0 | 0 | 0 | N |
AKAP12 | TQGADVSPD | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 477 | p.L482V | c.1444C>G | Missense_Mutation | 1 | 0.11 | HT | N | 0 | 0 | 0 | N |
AKAP12 | TQSGDTEAE | ENDOMETRIUM | 1204 | p.G1208D | c.3623G>A | Missense_Mutation | 1 | 0.11 | HEC1B | N | 0 | 0 | 0 | N |
AKAP12 | TQVPADFPD | ENDOMETRIUM | 548 | p.S554F | c.1661C>T | Missense_Mutation | 1 | 0.11 | JHUEM7 | N | 0 | 0 | 0 | Y |
AKAP12 | TRVPADSPD | STOMACH | 548 | p.Q549R | c.1646A>G | Missense_Mutation | 1 | 0.11 | 2313287 | N | 1 | 0 | 0 | N |
AKAP12 | TSWASFKKM | UPPER_AERODIGESTIVE_TRACT | 608 | p.P609S | c.1825C>T | Missense_Mutation | 1 | 0.11 | PECAPJ49 | N | 5 | 0 | 0 | N |
AKAP12 | TTEMLTSEL | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 1568 | p.A1568T | c.4702G>A | Missense_Mutation | 1 | 0.11 | HT | Y | 8 | 11 | 0 | N |
AKAP12 | TTKKGLSFD | SKIN | 1491 | p.S1498F | c.4493C>T | Missense_Mutation | 1 | 0.11 | MEWO | N | 0 | 0 | 0 | N |
AKAP12 | TTTEMLTSE | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 1567 | p.A1568T | c.4702G>A | Missense_Mutation | 1 | 0.11 | HT | N | 0 | 0 | 0 | N |
AKAP12 | TYVNEEKLE | LARGE_INTESTINE | 1351 | p.H1352Y | c.4054C>T | Missense_Mutation | 1 | 0.11 | LS123 | N | 0 | 0 | 0 | N |
AKAP12 | VAIEDLEPQ | LUNG | 1528 | p.E1536Q | c.4606G>C | Missense_Mutation | 1 | 0.11 | NCIH23 | N | 0 | 0 | 2 | N |
AKAP12 | VASGTQSGD | ENDOMETRIUM | 1200 | p.G1208D | c.3623G>A | Missense_Mutation | 1 | 0.11 | HEC1B | N | 0 | 0 | 0 | N |
AKAP12 | VDHDITDDG | UPPER_AERODIGESTIVE_TRACT | 130 | p.V131D | c.392T>A | Missense_Mutation | 1 | 0.11 | SNU46 | N | 0 | 0 | 0 | N |
AKAP12 | VDTKEDGKA | OESOPHAGUS | 335 | p.E338K | c.1012G>A | Missense_Mutation | 1 | 0.11 | KYSE410 | N | 4 | 0 | 0 | N |
AKAP12 | VEMEKMEAQ | LARGE_INTESTINE | 855 | p.R857M | c.2570G>T | Missense_Mutation | 1 | 0.11 | CW2 | N | 0 | 0 | 2 | N |
AKAP12 | VEPKEHEKG | LUNG | 1693 | p.D1698H | c.5092G>C | Missense_Mutation | 1 | 0.11 | NCIH23 | N | 0 | 0 | 0 | N |
AKAP12 | VETPTNSET | LUNG | 1163 | p.D1168N | c.3502G>A | Missense_Mutation | 1 | 0.11 | HCC366 | N | 5 | 0 | 0 | Y |
AKAP12 | VFDEKIDVH | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 403 | p.E409D | c.1227A>T | Missense_Mutation | 1 | 0.11 | WSUDLCL2 | N | 0 | 0 | 0 | N |
AKAP12 | VGQARSDIS | LARGE_INTESTINE | 1623 | p.H1627R | c.4880A>G | Missense_Mutation | 1 | 0.11 | CL11 | N | 1 | 0 | 0 | N |
AKAP12 | VIKANSQDA | LUNG | 1582 | p.D1586N | c.4756G>A | Missense_Mutation | 1 | 0.11 | NCIH23 | N | 1 | 0 | 4 | N |
AKAP12 | VLLSEYDAV | UPPER_AERODIGESTIVE_TRACT | 847 | p.P848L | c.2543C>T | Missense_Mutation | 1 | 0.11 | HS840T | Y | 9 | 11 | 0 | N |
AKAP12 | VLSKPPKGV | BREAST | 488 | p.E494K | c.1480G>A | Missense_Mutation | 1 | 0.11 | CAL148 | N | 6 | 0 | 10 | N |
AKAP12 | VNEEKLEYE | LUNG | 1353 | p.H1360Y | c.4078C>T | Missense_Mutation | 1 | 0.11 | NCIH2286 | N | 0 | 0 | 0 | N |
AKAP12 | VPADFPDSQ | ENDOMETRIUM | 550 | p.S554F | c.1661C>T | Missense_Mutation | 1 | 0.11 | JHUEM7 | N | 2 | 0 | 5 | Y |
AKAP12 | VPAMVPLSE | CENTRAL_NERVOUS_SYSTEM | 843 | p.V846M | c.2536G>A | Missense_Mutation | 1 | 0.11 | LN18 | N | 2 | 0 | 4 | N |
AKAP12 | VPAVVLLSE | UPPER_AERODIGESTIVE_TRACT | 843 | p.P848L | c.2543C>T | Missense_Mutation | 1 | 0.11 | HS840T | N | 2 | 0 | 0 | N |
AKAP12 | VQQDGEAEK | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 586 | p.E594K | c.1780G>A | Missense_Mutation | 1 | 0.11 | MOLT13 | N | 3 | 0 | 0 | N |
AKAP12 | VQRAEAQRP | LUNG | 1069 | p.E1075Q | c.3223G>C | Missense_Mutation | 1 | 0.11 | HCC78 | N | 0 | 0 | 1 | N |
AKAP12 | VRTEETTTE | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 1562 | p.A1568T | c.4702G>A | Missense_Mutation | 1 | 0.11 | HT | N | 1 | 0 | 6 | N |
AKAP12 | VSEKLTASE | ENDOMETRIUM | 346 | p.A346V | c.1037C>T | Missense_Mutation | 1 | 0.11 | MFE319 | N | 0 | 0 | 2 | N |
AKAP12 | VSERDSDKE | STOMACH | 115 | p.K117E | c.348_349CA>TG | Missense_Mutation | 1 | 0.11 | SNU1 | N | 0 | 0 | 0 | N |
AKAP12 | VSPDEKVLS | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 482 | p.L482V | c.1444C>G | Missense_Mutation | 1 | 0.11 | HT | N | 0 | 0 | 8 | N |
AKAP12 | VSREDPTQG | LIVER | 471 | p.G473R | c.1417G>A | Missense_Mutation | 1 | 0.11 | SNU449 | N | 0 | 0 | 0 | N |
AKAP12 | VTENIESSE | LARGE_INTESTINE | 1126 | p.S1129N | c.3386G>A | Missense_Mutation | 1 | 0.11 | KM12 | N | 0 | 0 | 0 | N |
AKAP12 | VTSWASFKK | UPPER_AERODIGESTIVE_TRACT | 607 | p.P609S | c.1825C>T | Missense_Mutation | 1 | 0.11 | PECAPJ49 | N | 5 | 0 | 1 | N |
AKAP12 | VVLLSEYDA | UPPER_AERODIGESTIVE_TRACT | 846 | p.P848L | c.2543C>T | Missense_Mutation | 1 | 0.11 | HS840T | N | 5 | 0 | 12 | N |
AKAP12 | VVSEKLTAS | ENDOMETRIUM | 345 | p.A346V | c.1037C>T | Missense_Mutation | 1 | 0.11 | MFE319 | N | 0 | 0 | 8 | N |
AKAP12 | WSSSDEEGG | ENDOMETRIUM | 695 | p.G695W | c.2083G>T | Missense_Mutation | 1 | 0.11 | SNGM | N | 1 | 0 | 0 | N |
AKAP12 | YDAVEMEKM | LARGE_INTESTINE | 852 | p.R857M | c.2570G>T | Missense_Mutation | 1 | 0.11 | CW2 | N | 8 | 0 | 0 | N |
AKAP12 | YETAVTVSE | LUNG | 1360 | p.H1360Y | c.4078C>T | Missense_Mutation | 1 | 0.11 | NCIH2286 | N | 2 | 0 | 1 | N |
AKAP12 | YVNEEKLEH | LARGE_INTESTINE | 1352 | p.H1352Y | c.4054C>T | Missense_Mutation | 1 | 0.11 | LS123 | N | 1 | 0 | 31 | N |
AKAP12 | AEQNELSLQ | BREAST | 69 | p.D72N | c.214G>A | Missense_Mutation | 1 | 0.22 | HCC1954 | N | 0 | 0 | 0 | Y |
AKAP12 | AEQNELSLQ | LARGE_INTESTINE | 69 | p.D72N | c.214G>A | Missense_Mutation | 1 | 0.22 | HS698T | N | 0 | 0 | 0 | Y |
AKAP12 | CIPGRRKKR | CENTRAL_NERVOUS_SYSTEM | 810 | p.F810C | c.2429T>G | Missense_Mutation | 1 | 0.22 | GMS10 | N | 3 | 0 | 0 | N |
AKAP12 | CIPGRRKKR | SKIN | 810 | p.F810C | c.2429T>G | Missense_Mutation | 1 | 0.22 | SKMEL24 | N | 3 | 0 | 0 | N |
AKAP12 | EKVLSKPPK | BREAST | 486 | p.E494K | c.1480G>A | Missense_Mutation | 1 | 0.22 | CAL148 | N | 1 | 0 | 0 | N |
AKAP12 | EQNELSLQE | BREAST | 70 | p.D72N | c.214G>A | Missense_Mutation | 1 | 0.22 | HCC1954 | N | 0 | 0 | 0 | N |
AKAP12 | EQNELSLQE | LARGE_INTESTINE | 70 | p.D72N | c.214G>A | Missense_Mutation | 1 | 0.22 | HS698T | N | 0 | 0 | 0 | N |
AKAP12 | ESWVSIKKC | CENTRAL_NERVOUS_SYSTEM | 802 | p.F810C | c.2429T>G | Missense_Mutation | 1 | 0.22 | GMS10 | N | 1 | 0 | 0 | N |
AKAP12 | ESWVSIKKC | SKIN | 802 | p.F810C | c.2429T>G | Missense_Mutation | 1 | 0.22 | SKMEL24 | N | 1 | 0 | 0 | N |
AKAP12 | GVAEQNELS | BREAST | 67 | p.D72N | c.214G>A | Missense_Mutation | 1 | 0.22 | HCC1954 | N | 0 | 0 | 0 | N |
AKAP12 | GVAEQNELS | LARGE_INTESTINE | 67 | p.D72N | c.214G>A | Missense_Mutation | 1 | 0.22 | HS698T | N | 0 | 0 | 0 | N |
AKAP12 | IKKCIPGRR | CENTRAL_NERVOUS_SYSTEM | 807 | p.F810C | c.2429T>G | Missense_Mutation | 1 | 0.22 | GMS10 | N | 1 | 0 | 2 | N |
AKAP12 | IKKCIPGRR | SKIN | 807 | p.F810C | c.2429T>G | Missense_Mutation | 1 | 0.22 | SKMEL24 | N | 1 | 0 | 2 | N |
AKAP12 | INGVAEQNE | BREAST | 65 | p.D72N | c.214G>A | Missense_Mutation | 1 | 0.22 | HCC1954 | N | 0 | 0 | 0 | N |
AKAP12 | INGVAEQNE | LARGE_INTESTINE | 65 | p.D72N | c.214G>A | Missense_Mutation | 1 | 0.22 | HS698T | N | 0 | 0 | 0 | N |
AKAP12 | KCIPGRRKK | CENTRAL_NERVOUS_SYSTEM | 809 | p.F810C | c.2429T>G | Missense_Mutation | 1 | 0.22 | GMS10 | Y | 2 | 13 | 0 | N |
AKAP12 | KCIPGRRKK | SKIN | 809 | p.F810C | c.2429T>G | Missense_Mutation | 1 | 0.22 | SKMEL24 | Y | 2 | 13 | 0 | N |
AKAP12 | KKCIPGRRK | CENTRAL_NERVOUS_SYSTEM | 808 | p.F810C | c.2429T>G | Missense_Mutation | 1 | 0.22 | GMS10 | N | 1 | 0 | 0 | N |
AKAP12 | KKCIPGRRK | SKIN | 808 | p.F810C | c.2429T>G | Missense_Mutation | 1 | 0.22 | SKMEL24 | N | 1 | 0 | 0 | N |
AKAP12 | KKRVRWPSE | PROSTATE | 620 | p.R625W | c.1873C>T | Missense_Mutation | 1 | 0.22 | NCIH660 | N | 1 | 0 | 0 | N |
AKAP12 | KKRVRWPSE | SOFT_TISSUE | 620 | p.R625W | c.1873C>T | Missense_Mutation | 1 | 0.22 | SJRH30 | N | 1 | 0 | 0 | N |
AKAP12 | KRVRWPSES | PROSTATE | 621 | p.R625W | c.1873C>T | Missense_Mutation | 1 | 0.22 | NCIH660 | N | 2 | 0 | 0 | N |
AKAP12 | KRVRWPSES | SOFT_TISSUE | 621 | p.R625W | c.1873C>T | Missense_Mutation | 1 | 0.22 | SJRH30 | N | 2 | 0 | 0 | N |
AKAP12 | NELSLQEGD | BREAST | 72 | p.D72N | c.214G>A | Missense_Mutation | 1 | 0.22 | HCC1954 | N | 0 | 0 | 0 | N |
AKAP12 | NELSLQEGD | LARGE_INTESTINE | 72 | p.D72N | c.214G>A | Missense_Mutation | 1 | 0.22 | HS698T | N | 0 | 0 | 0 | N |
AKAP12 | NGVAEQNEL | BREAST | 66 | p.D72N | c.214G>A | Missense_Mutation | 1 | 0.22 | HCC1954 | N | 13 | 0 | 0 | N |
AKAP12 | NGVAEQNEL | LARGE_INTESTINE | 66 | p.D72N | c.214G>A | Missense_Mutation | 1 | 0.22 | HS698T | N | 13 | 0 | 0 | N |
AKAP12 | PKKRVRWPS | PROSTATE | 619 | p.R625W | c.1873C>T | Missense_Mutation | 1 | 0.22 | NCIH660 | N | 0 | 0 | 0 | N |
AKAP12 | PKKRVRWPS | SOFT_TISSUE | 619 | p.R625W | c.1873C>T | Missense_Mutation | 1 | 0.22 | SJRH30 | N | 0 | 0 | 0 | N |
AKAP12 | QNELSLQEG | BREAST | 71 | p.D72N | c.214G>A | Missense_Mutation | 1 | 0.22 | HCC1954 | N | 0 | 0 | 0 | N |
AKAP12 | QNELSLQEG | LARGE_INTESTINE | 71 | p.D72N | c.214G>A | Missense_Mutation | 1 | 0.22 | HS698T | N | 0 | 0 | 0 | N |
AKAP12 | RVRWPSESD | PROSTATE | 622 | p.R625W | c.1873C>T | Missense_Mutation | 1 | 0.22 | NCIH660 | N | 0 | 0 | 0 | N |
AKAP12 | RVRWPSESD | SOFT_TISSUE | 622 | p.R625W | c.1873C>T | Missense_Mutation | 1 | 0.22 | SJRH30 | N | 0 | 0 | 0 | N |
AKAP12 | RWPSESDKE | PROSTATE | 624 | p.R625W | c.1873C>T | Missense_Mutation | 1 | 0.22 | NCIH660 | N | 0 | 0 | 0 | N |
AKAP12 | RWPSESDKE | SOFT_TISSUE | 624 | p.R625W | c.1873C>T | Missense_Mutation | 1 | 0.22 | SJRH30 | N | 0 | 0 | 0 | N |
AKAP12 | SIKKCIPGR | CENTRAL_NERVOUS_SYSTEM | 806 | p.F810C | c.2429T>G | Missense_Mutation | 1 | 0.22 | GMS10 | N | 5 | 0 | 0 | N |
AKAP12 | SIKKCIPGR | SKIN | 806 | p.F810C | c.2429T>G | Missense_Mutation | 1 | 0.22 | SKMEL24 | N | 5 | 0 | 0 | N |
AKAP12 | SWVSIKKCI | CENTRAL_NERVOUS_SYSTEM | 803 | p.F810C | c.2429T>G | Missense_Mutation | 1 | 0.22 | GMS10 | N | 7 | 0 | 0 | N |
AKAP12 | SWVSIKKCI | SKIN | 803 | p.F810C | c.2429T>G | Missense_Mutation | 1 | 0.22 | SKMEL24 | N | 7 | 0 | 0 | N |
AKAP12 | TINGVAEQN | BREAST | 64 | p.D72N | c.214G>A | Missense_Mutation | 1 | 0.22 | HCC1954 | N | 0 | 0 | 0 | N |
AKAP12 | TINGVAEQN | LARGE_INTESTINE | 64 | p.D72N | c.214G>A | Missense_Mutation | 1 | 0.22 | HS698T | N | 0 | 0 | 0 | N |
AKAP12 | TPKKRVRWP | PROSTATE | 618 | p.R625W | c.1873C>T | Missense_Mutation | 1 | 0.22 | NCIH660 | N | 2 | 0 | 0 | N |
AKAP12 | TPKKRVRWP | SOFT_TISSUE | 618 | p.R625W | c.1873C>T | Missense_Mutation | 1 | 0.22 | SJRH30 | N | 2 | 0 | 0 | N |
AKAP12 | VAEQNELSL | BREAST | 68 | p.D72N | c.214G>A | Missense_Mutation | 1 | 0.22 | HCC1954 | N | 12 | 0 | 0 | N |
AKAP12 | VAEQNELSL | LARGE_INTESTINE | 68 | p.D72N | c.214G>A | Missense_Mutation | 1 | 0.22 | HS698T | N | 12 | 0 | 0 | N |
AKAP12 | VRWPSESDK | PROSTATE | 623 | p.R625W | c.1873C>T | Missense_Mutation | 1 | 0.22 | NCIH660 | N | 2 | 0 | 0 | N |
AKAP12 | VRWPSESDK | SOFT_TISSUE | 623 | p.R625W | c.1873C>T | Missense_Mutation | 1 | 0.22 | SJRH30 | N | 2 | 0 | 0 | N |
AKAP12 | VSIKKCIPG | CENTRAL_NERVOUS_SYSTEM | 805 | p.F810C | c.2429T>G | Missense_Mutation | 1 | 0.22 | GMS10 | N | 0 | 0 | 4 | Y |
AKAP12 | VSIKKCIPG | SKIN | 805 | p.F810C | c.2429T>G | Missense_Mutation | 1 | 0.22 | SKMEL24 | N | 0 | 0 | 4 | Y |
AKAP12 | VTPKKRVRW | PROSTATE | 617 | p.R625W | c.1873C>T | Missense_Mutation | 1 | 0.22 | NCIH660 | N | 3 | 0 | 1 | N |
AKAP12 | VTPKKRVRW | SOFT_TISSUE | 617 | p.R625W | c.1873C>T | Missense_Mutation | 1 | 0.22 | SJRH30 | N | 3 | 0 | 1 | N |
AKAP12 | WPSESDKED | PROSTATE | 625 | p.R625W | c.1873C>T | Missense_Mutation | 1 | 0.22 | NCIH660 | N | 3 | 0 | 0 | N |
AKAP12 | WPSESDKED | SOFT_TISSUE | 625 | p.R625W | c.1873C>T | Missense_Mutation | 1 | 0.22 | SJRH30 | N | 3 | 0 | 0 | N |
AKAP12 | WVSIKKCIP | CENTRAL_NERVOUS_SYSTEM | 804 | p.F810C | c.2429T>G | Missense_Mutation | 1 | 0.22 | GMS10 | N | 2 | 0 | 19 | N |
AKAP12 | WVSIKKCIP | SKIN | 804 | p.F810C | c.2429T>G | Missense_Mutation | 1 | 0.22 | SKMEL24 | N | 2 | 0 | 19 | N |