RET | ACSQDGPAP | LUNG | 793 | p.G798fs | c.2393_2394insC | Frame_Shift_Ins | 2 | 0.11 | NCIH2347 | N | 0 | 0 | 0 | Y |
RET | AGLPPREPQ | LUNG | 813 | p.G798fs | c.2393_2394insC | Frame_Shift_Ins | 5 | 0.11 | NCIH2347 | N | 0 | 0 | 0 | Y |
RET | APPHRGVRQ | LUNG | 800 | p.G798fs | c.2393_2394insC | Frame_Shift_Ins | 6 | 0.11 | NCIH2347 | N | 0 | 0 | 0 | Y |
RET | APPPSSPPF | LARGE_INTESTINE | 1046 | p.A1046fs | c.3136_3137insC | Frame_Shift_Ins | 5 | 0.11 | LS411N | N | 13 | 0 | 0 | N |
RET | AWLPGQWRQ | LUNG | 824 | p.G798fs | c.2393_2394insC | Frame_Shift_Ins | 5 | 0.11 | NCIH2347 | N | 0 | 0 | 0 | N |
RET | CNNAPPPSS | LARGE_INTESTINE | 1043 | p.A1046fs | c.3136_3137insC | Frame_Shift_Ins | 3 | 0.11 | LS411N | N | 0 | 0 | 0 | N |
RET | CSQDGPAPP | LUNG | 794 | p.G798fs | c.2393_2394insC | Frame_Shift_Ins | 3 | 0.11 | NCIH2347 | N | 0 | 0 | 0 | Y |
RET | DCNNAPPPS | LARGE_INTESTINE | 1042 | p.A1046fs | c.3136_3137insC | Frame_Shift_Ins | 2 | 0.11 | LS411N | N | 0 | 0 | 0 | Y |
RET | DGPAPPHRG | LUNG | 797 | p.G798fs | c.2393_2394insC | Frame_Shift_Ins | 6 | 0.11 | NCIH2347 | N | 1 | 0 | 0 | Y |
RET | EPQSGAWLP | LUNG | 819 | p.G798fs | c.2393_2394insC | Frame_Shift_Ins | 5 | 0.11 | NCIH2347 | N | 1 | 0 | 0 | N |
RET | GACSQDGPA | LUNG | 792 | p.G798fs | c.2393_2394insC | Frame_Shift_Ins | 1 | 0.11 | NCIH2347 | N | 1 | 0 | 0 | N |
RET | GAWLPGQWR | LUNG | 823 | p.G798fs | c.2393_2394insC | Frame_Shift_Ins | 5 | 0.11 | NCIH2347 | N | 7 | 0 | 0 | N |
RET | GLPPREPQS | LUNG | 814 | p.G798fs | c.2393_2394insC | Frame_Shift_Ins | 5 | 0.11 | NCIH2347 | N | 1 | 0 | 0 | Y |
RET | GPAPPHRGV | LUNG | 798 | p.G798fs | c.2393_2394insC | Frame_Shift_Ins | 6 | 0.11 | NCIH2347 | Y | 13 | 12 | 0 | Y |
RET | GQWRQPQLQ | LUNG | 828 | p.G798fs | c.2393_2394insC | Frame_Shift_Ins | 5 | 0.11 | NCIH2347 | N | 0 | 0 | 0 | N |
RET | GVRQIRLPA | LUNG | 805 | p.G798fs | c.2393_2394insC | Frame_Shift_Ins | 6 | 0.11 | NCIH2347 | N | 2 | 0 | 0 | N |
RET | HRGVRQIRL | LUNG | 803 | p.G798fs | c.2393_2394insC | Frame_Shift_Ins | 6 | 0.11 | NCIH2347 | Y | 7 | 10 | 0 | N |
RET | IRLPAGLPP | LUNG | 809 | p.G798fs | c.2393_2394insC | Frame_Shift_Ins | 5 | 0.11 | NCIH2347 | N | 1 | 0 | 2 | N |
RET | LPAGLPPRE | LUNG | 811 | p.G798fs | c.2393_2394insC | Frame_Shift_Ins | 5 | 0.11 | NCIH2347 | N | 1 | 0 | 0 | N |
RET | LPGQWRQPQ | LUNG | 826 | p.G798fs | c.2393_2394insC | Frame_Shift_Ins | 5 | 0.11 | NCIH2347 | N | 2 | 0 | 0 | N |
RET | LPPREPQSG | LUNG | 815 | p.G798fs | c.2393_2394insC | Frame_Shift_Ins | 5 | 0.11 | NCIH2347 | N | 1 | 0 | 0 | Y |
RET | LVDCNNAPP | LARGE_INTESTINE | 1040 | p.A1046fs | c.3136_3137insC | Frame_Shift_Ins | 1 | 0.11 | LS411N | N | 0 | 0 | 0 | N |
RET | NAPPPSSPP | LARGE_INTESTINE | 1045 | p.A1046fs | c.3136_3137insC | Frame_Shift_Ins | 4 | 0.11 | LS411N | N | 0 | 0 | 0 | N |
RET | NNAPPPSSP | LARGE_INTESTINE | 1044 | p.A1046fs | c.3136_3137insC | Frame_Shift_Ins | 4 | 0.11 | LS411N | N | 0 | 0 | 0 | N |
RET | PAGLPPREP | LUNG | 812 | p.G798fs | c.2393_2394insC | Frame_Shift_Ins | 5 | 0.11 | NCIH2347 | N | 0 | 0 | 0 | N |
RET | PAPPHRGVR | LUNG | 799 | p.G798fs | c.2393_2394insC | Frame_Shift_Ins | 6 | 0.11 | NCIH2347 | N | 0 | 0 | 0 | Y |
RET | PGQWRQPQL | LUNG | 827 | p.G798fs | c.2393_2394insC | Frame_Shift_Ins | 5 | 0.11 | NCIH2347 | N | 1 | 0 | 0 | N |
RET | PHRGVRQIR | LUNG | 802 | p.G798fs | c.2393_2394insC | Frame_Shift_Ins | 6 | 0.11 | NCIH2347 | N | 0 | 0 | 0 | N |
RET | PPHRGVRQI | LUNG | 801 | p.G798fs | c.2393_2394insC | Frame_Shift_Ins | 6 | 0.11 | NCIH2347 | Y | 7 | 13 | 0 | N |
RET | PPPSSPPFH | LARGE_INTESTINE | 1047 | p.A1046fs | c.3136_3137insC | Frame_Shift_Ins | 5 | 0.11 | LS411N | N | 0 | 0 | 0 | N |
RET | PPREPQSGA | LUNG | 816 | p.G798fs | c.2393_2394insC | Frame_Shift_Ins | 5 | 0.11 | NCIH2347 | N | 4 | 0 | 0 | Y |
RET | PPSSPPFHM | LARGE_INTESTINE | 1048 | p.A1046fs | c.3136_3137insC | Frame_Shift_Ins | 6 | 0.11 | LS411N | N | 5 | 0 | 0 | N |
RET | PQLQLPGPP | LUNG | 833 | p.G798fs | c.2393_2394insC | Frame_Shift_Ins | 5 | 0.11 | NCIH2347 | N | 0 | 0 | 0 | N |
RET | PQSGAWLPG | LUNG | 820 | p.G798fs | c.2393_2394insC | Frame_Shift_Ins | 5 | 0.11 | NCIH2347 | N | 0 | 0 | 0 | N |
RET | PREPQSGAW | LUNG | 817 | p.G798fs | c.2393_2394insC | Frame_Shift_Ins | 6 | 0.11 | NCIH2347 | N | 1 | 0 | 0 | N |
RET | PSSPPFHMD | LARGE_INTESTINE | 1049 | p.A1046fs | c.3136_3137insC | Frame_Shift_Ins | 5 | 0.11 | LS411N | N | 0 | 0 | 0 | N |
RET | QDGPAPPHR | LUNG | 796 | p.G798fs | c.2393_2394insC | Frame_Shift_Ins | 5 | 0.11 | NCIH2347 | N | 0 | 0 | 0 | Y |
RET | QIRLPAGLP | LUNG | 808 | p.G798fs | c.2393_2394insC | Frame_Shift_Ins | 5 | 0.11 | NCIH2347 | N | 0 | 0 | 0 | N |
RET | QLQLPGPPG | LUNG | 834 | p.G798fs | c.2393_2394insC | Frame_Shift_Ins | 6 | 0.11 | NCIH2347 | N | 0 | 0 | 0 | N |
RET | QPQLQLPGP | LUNG | 832 | p.G798fs | c.2393_2394insC | Frame_Shift_Ins | 5 | 0.11 | NCIH2347 | N | 0 | 0 | 0 | N |
RET | QSGAWLPGQ | LUNG | 821 | p.G798fs | c.2393_2394insC | Frame_Shift_Ins | 5 | 0.11 | NCIH2347 | N | 0 | 0 | 0 | N |
RET | QWRQPQLQL | LUNG | 829 | p.G798fs | c.2393_2394insC | Frame_Shift_Ins | 4 | 0.11 | NCIH2347 | N | 3 | 0 | 0 | N |
RET | REPQSGAWL | LUNG | 818 | p.G798fs | c.2393_2394insC | Frame_Shift_Ins | 6 | 0.11 | NCIH2347 | Y | 12 | 10 | 0 | N |
RET | RGVRQIRLP | LUNG | 804 | p.G798fs | c.2393_2394insC | Frame_Shift_Ins | 6 | 0.11 | NCIH2347 | N | 0 | 0 | 0 | N |
RET | RLPAGLPPR | LUNG | 810 | p.G798fs | c.2393_2394insC | Frame_Shift_Ins | 5 | 0.11 | NCIH2347 | N | 7 | 0 | 0 | N |
RET | RQIRLPAGL | LUNG | 807 | p.G798fs | c.2393_2394insC | Frame_Shift_Ins | 6 | 0.11 | NCIH2347 | N | 16 | 0 | 0 | N |
RET | RQPQLQLPG | LUNG | 831 | p.G798fs | c.2393_2394insC | Frame_Shift_Ins | 4 | 0.11 | NCIH2347 | N | 0 | 0 | 0 | N |
RET | SGAWLPGQW | LUNG | 822 | p.G798fs | c.2393_2394insC | Frame_Shift_Ins | 5 | 0.11 | NCIH2347 | N | 2 | 0 | 0 | N |
RET | SQDGPAPPH | LUNG | 795 | p.G798fs | c.2393_2394insC | Frame_Shift_Ins | 4 | 0.11 | NCIH2347 | N | 1 | 0 | 0 | N |
RET | VDCNNAPPP | LARGE_INTESTINE | 1041 | p.A1046fs | c.3136_3137insC | Frame_Shift_Ins | 1 | 0.11 | LS411N | N | 0 | 0 | 0 | Y |
RET | VRQIRLPAG | LUNG | 806 | p.G798fs | c.2393_2394insC | Frame_Shift_Ins | 6 | 0.11 | NCIH2347 | N | 1 | 0 | 10 | N |
RET | WLPGQWRQP | LUNG | 825 | p.G798fs | c.2393_2394insC | Frame_Shift_Ins | 5 | 0.11 | NCIH2347 | N | 2 | 0 | 0 | N |
RET | WRQPQLQLP | LUNG | 830 | p.G798fs | c.2393_2394insC | Frame_Shift_Ins | 4 | 0.11 | NCIH2347 | N | 3 | 0 | 0 | N |
RET | AAKLMDTYD | URINARY_TRACT | 1105 | p.F1112Y | c.3335T>A | Missense_Mutation | 1 | 0.11 | J82 | N | 0 | 0 | 0 | N |
RET | AATVLFSFI | OVARY | 639 | p.A641T | c.1921G>A | Missense_Mutation | 1 | 0.11 | OVK18 | Y | 9 | 10 | 0 | N |
RET | ADINKDLEK | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 999 | p.S1002N | c.3005G>A | Missense_Mutation | 1 | 0.11 | DND41 | N | 0 | 0 | 0 | Y |
RET | AFHLKGRTG | OVARY | 743 | p.A750T | c.2248G>A | Missense_Mutation | 1 | 0.11 | IGROV1 | N | 0 | 0 | 0 | N |
RET | AFHMKGRAG | PROSTATE | 743 | p.L746M | c.2236C>A | Missense_Mutation | 1 | 0.11 | DU145 | N | 0 | 0 | 0 | N |
RET | AFPSELRDL | SKIN | 764 | p.S765F | c.2294C>T | Missense_Mutation | 1 | 0.11 | MELJUSO | Y | 8 | 10 | 0 | N |
RET | AFPVSYYSS | LUNG | 682 | p.S688Y | c.2063C>A | Missense_Mutation | 1 | 0.11 | HARA | N | 1 | 0 | 0 | N |
RET | AHRPSLDSM | OVARY | 692 | p.R693H | c.2078G>A | Missense_Mutation | 1 | 0.11 | JHOM2B | N | 2 | 0 | 0 | N |
RET | AKLHYMVVA | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 479 | p.E480K | c.1438G>A | Missense_Mutation | 1 | 0.11 | HS611T | N | 2 | 0 | 0 | N |
RET | AKLMDTYDS | URINARY_TRACT | 1106 | p.F1112Y | c.3335T>A | Missense_Mutation | 1 | 0.11 | J82 | N | 1 | 0 | 0 | N |
RET | ALRRPKCAK | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 472 | p.E480K | c.1438G>A | Missense_Mutation | 1 | 0.11 | HS611T | Y | 4 | 15 | 0 | N |
RET | ALTMGDLIT | LUNG | 845 | p.S853T | c.2557T>A | Missense_Mutation | 1 | 0.11 | NCIH2066 | N | 1 | 0 | 0 | N |
RET | ANWMLSPSV | LUNG | 1097 | p.A1105V | c.3314C>T | Missense_Mutation | 1 | 0.11 | NCIH1092 | N | 8 | 0 | 0 | N |
RET | APFPRALPS | ENDOMETRIUM | 1046 | p.L1048F | c.3142C>T | Missense_Mutation | 1 | 0.11 | TEN | N | 7 | 0 | 0 | N |
RET | APLVDCNNA | LARGE_INTESTINE | 1038 | p.T1038A | c.3112A>G | Missense_Mutation | 1 | 0.11 | SNU175 | N | 10 | 0 | 0 | N |
RET | AQAFPVSYY | LUNG | 680 | p.S688Y | c.2063C>A | Missense_Mutation | 1 | 0.11 | HARA | Y | 7 | 13 | 0 | N |
RET | AQIGKVCVK | LUNG | 420 | p.E428K | c.1282G>A | Missense_Mutation | 1 | 0.11 | NCIH1339 | Y | 5 | 15 | 0 | N |
RET | AQLLVTVEE | UPPER_AERODIGESTIVE_TRACT | 498 | p.G506E | c.1517G>A | Missense_Mutation | 1 | 0.11 | SNU1076 | N | 0 | 0 | 0 | N |
RET | ARRASLDSM | ENDOMETRIUM | 692 | p.P695A | c.2083C>G | Missense_Mutation | 1 | 0.11 | EN | Y | 2 | 9 | 0 | N |
RET | ASLDSMENQ | ENDOMETRIUM | 695 | p.P695A | c.2083C>G | Missense_Mutation | 1 | 0.11 | EN | N | 0 | 0 | 0 | N |
RET | ATAFHMKGR | PROSTATE | 741 | p.L746M | c.2236C>A | Missense_Mutation | 1 | 0.11 | DU145 | Y | 3 | 14 | 0 | N |
RET | ATVLFSFIV | OVARY | 640 | p.A641T | c.1921G>A | Missense_Mutation | 1 | 0.11 | OVK18 | Y | 6 | 9 | 0 | N |
RET | AVVLLLHFN | LUNG | 386 | p.G387V | c.1160G>T | Missense_Mutation | 1 | 0.11 | HARA | N | 0 | 0 | 0 | N |
RET | AWQTSQGMQ | PROSTATE | 855 | p.I858T | c.2573T>C | Missense_Mutation | 1 | 0.11 | LNCAPCLONEFGC | N | 0 | 0 | 0 | N |
RET | CAKLHYMVV | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 478 | p.E480K | c.1438G>A | Missense_Mutation | 1 | 0.11 | HS611T | N | 7 | 0 | 0 | N |
RET | CDELCRTMI | CENTRAL_NERVOUS_SYSTEM | 630 | p.V637M | c.1909G>A | Missense_Mutation | 1 | 0.11 | KNS42 | N | 2 | 0 | 0 | N |
RET | CDELWRTVI | THYROID | 630 | p.C634W | c.1902C>G | Missense_Mutation | 1 | 0.11 | TT | N | 3 | 0 | 0 | N |
RET | CLHLPSTYS | SKIN | 401 | p.S401C | c.1201A>T | Missense_Mutation | 1 | 0.11 | RPMI7951 | N | 0 | 0 | 0 | N |
RET | CNNAPFPRA | ENDOMETRIUM | 1043 | p.L1048F | c.3142C>T | Missense_Mutation | 1 | 0.11 | TEN | N | 0 | 0 | 0 | N |
RET | CRTMIAAAV | CENTRAL_NERVOUS_SYSTEM | 634 | p.V637M | c.1909G>A | Missense_Mutation | 1 | 0.11 | KNS42 | N | 3 | 0 | 0 | N |
RET | CRTVIAATV | OVARY | 634 | p.A641T | c.1921G>A | Missense_Mutation | 1 | 0.11 | OVK18 | Y | 3 | 10 | 0 | N |
RET | CSPITKTCP | LARGE_INTESTINE | 558 | p.S561I | c.1682G>T | Missense_Mutation | 1 | 0.11 | T84 | N | 0 | 0 | 0 | N |
RET | CVKNCQAFS | LUNG | 426 | p.E428K | c.1282G>A | Missense_Mutation | 1 | 0.11 | NCIH1339 | N | 0 | 0 | 0 | N |
RET | CWKQKPDKR | LARGE_INTESTINE | 987 | p.E991K | c.2971G>A | Missense_Mutation | 1 | 0.11 | SKCO1 | N | 1 | 0 | 0 | Y |
RET | DCNNAPFPR | ENDOMETRIUM | 1042 | p.L1048F | c.3142C>T | Missense_Mutation | 1 | 0.11 | TEN | N | 3 | 0 | 0 | N |
RET | DDGLSEEEA | LARGE_INTESTINE | 1030 | p.T1038A | c.3112A>G | Missense_Mutation | 1 | 0.11 | SNU175 | N | 5 | 0 | 0 | Y |
RET | DELCRTMIA | CENTRAL_NERVOUS_SYSTEM | 631 | p.V637M | c.1909G>A | Missense_Mutation | 1 | 0.11 | KNS42 | N | 5 | 0 | 0 | N |
RET | DELWRTVIA | THYROID | 631 | p.C634W | c.1902C>G | Missense_Mutation | 1 | 0.11 | TT | N | 5 | 0 | 0 | N |
RET | DEWALTMGD | LARGE_INTESTINE | 842 | p.R844W | c.2530C>T | Missense_Mutation | 1 | 0.11 | SNUC2A | N | 1 | 0 | 0 | Y |
RET | DFQGPGAVV | LUNG | 380 | p.G387V | c.1160G>T | Missense_Mutation | 1 | 0.11 | HARA | N | 3 | 0 | 0 | N |
RET | DGLSEEEAP | LARGE_INTESTINE | 1031 | p.T1038A | c.3112A>G | Missense_Mutation | 1 | 0.11 | SNU175 | N | 0 | 0 | 0 | Y |
RET | DHPDEWALT | LARGE_INTESTINE | 839 | p.R844W | c.2530C>T | Missense_Mutation | 1 | 0.11 | SNUC2A | N | 2 | 0 | 0 | N |
RET | DINKDLEKM | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 1000 | p.S1002N | c.3005G>A | Missense_Mutation | 1 | 0.11 | DND41 | N | 2 | 0 | 0 | Y |
RET | DLISFAWQT | PROSTATE | 850 | p.I858T | c.2573T>C | Missense_Mutation | 1 | 0.11 | LNCAPCLONEFGC | N | 3 | 0 | 0 | N |
RET | DLITFAWQI | LUNG | 850 | p.S853T | c.2557T>A | Missense_Mutation | 1 | 0.11 | NCIH2066 | N | 10 | 0 | 0 | N |
RET | DPLCDELWR | THYROID | 627 | p.C634W | c.1902C>G | Missense_Mutation | 1 | 0.11 | TT | N | 4 | 0 | 0 | N |
RET | DQTAGTPLL | LARGE_INTESTINE | 43 | p.A45T | c.133G>A | Missense_Mutation | 1 | 0.11 | CW2 | N | 6 | 0 | 0 | N |
RET | DYLELAAST | LUNG | 1014 | p.D1017E | c.3051C>G | Missense_Mutation | 1 | 0.11 | HARA | N | 4 | 0 | 0 | N |
RET | DYRLVLNWN | LARGE_INTESTINE | 353 | p.R360W | c.1078C>T | Missense_Mutation | 1 | 0.11 | SW48 | N | 2 | 0 | 0 | N |
RET | EAPLVDCNN | LARGE_INTESTINE | 1037 | p.T1038A | c.3112A>G | Missense_Mutation | 1 | 0.11 | SNU175 | N | 2 | 0 | 0 | N |
RET | EEAPLVDCN | LARGE_INTESTINE | 1036 | p.T1038A | c.3112A>G | Missense_Mutation | 1 | 0.11 | SNU175 | N | 4 | 0 | 0 | N |
RET | EEEAPLVDC | LARGE_INTESTINE | 1035 | p.T1038A | c.3112A>G | Missense_Mutation | 1 | 0.11 | SNU175 | N | 5 | 0 | 0 | N |
RET | EESYVAEEA | UPPER_AERODIGESTIVE_TRACT | 505 | p.G506E | c.1517G>A | Missense_Mutation | 1 | 0.11 | SNU1076 | Y | 6 | 11 | 0 | Y |
RET | EKLYVDQTA | LARGE_INTESTINE | 38 | p.A45T | c.133G>A | Missense_Mutation | 1 | 0.11 | CW2 | N | 2 | 0 | 0 | N |
RET | ELAASTPSD | LUNG | 1017 | p.D1017E | c.3051C>G | Missense_Mutation | 1 | 0.11 | HARA | N | 0 | 0 | 0 | N |
RET | ELCRTMIAA | CENTRAL_NERVOUS_SYSTEM | 632 | p.V637M | c.1909G>A | Missense_Mutation | 1 | 0.11 | KNS42 | Y | 2 | 11 | 0 | N |
RET | ELWRTVIAA | THYROID | 632 | p.C634W | c.1902C>G | Missense_Mutation | 1 | 0.11 | TT | Y | 5 | 12 | 0 | N |
RET | ENAFPSELR | SKIN | 762 | p.S765F | c.2294C>T | Missense_Mutation | 1 | 0.11 | MELJUSO | N | 3 | 0 | 0 | N |
RET | ESYVAEEAG | UPPER_AERODIGESTIVE_TRACT | 506 | p.G506E | c.1517G>A | Missense_Mutation | 1 | 0.11 | SNU1076 | N | 0 | 0 | 0 | N |
RET | EWALTMGDL | LARGE_INTESTINE | 843 | p.R844W | c.2530C>T | Missense_Mutation | 1 | 0.11 | SNUC2A | N | 4 | 0 | 0 | Y |
RET | FADINKDLE | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 998 | p.S1002N | c.3005G>A | Missense_Mutation | 1 | 0.11 | DND41 | N | 2 | 0 | 0 | Y |
RET | FAWQTSQGM | PROSTATE | 854 | p.I858T | c.2573T>C | Missense_Mutation | 1 | 0.11 | LNCAPCLONEFGC | Y | 8 | 9 | 1 | N |
RET | FHLKGRTGY | OVARY | 744 | p.A750T | c.2248G>A | Missense_Mutation | 1 | 0.11 | IGROV1 | N | 5 | 0 | 8 | N |
RET | FHLLPVQFL | LARGE_INTESTINE | 188 | p.R189H | c.566G>A | Missense_Mutation | 1 | 0.11 | T84 | Y | 14 | 11 | 25 | N |
RET | FHMKGRAGY | PROSTATE | 744 | p.L746M | c.2236C>A | Missense_Mutation | 1 | 0.11 | DU145 | N | 5 | 0 | 23 | N |
RET | FHQFHLLPV | LARGE_INTESTINE | 185 | p.R189H | c.566G>A | Missense_Mutation | 1 | 0.11 | T84 | N | 6 | 0 | 13 | N |
RET | FNVSVLPVC | SKIN | 393 | p.S401C | c.1201A>T | Missense_Mutation | 1 | 0.11 | RPMI7951 | N | 2 | 0 | 2 | N |
RET | FPRALPSTW | ENDOMETRIUM | 1048 | p.L1048F | c.3142C>T | Missense_Mutation | 1 | 0.11 | TEN | N | 8 | 0 | 0 | N |
RET | FPSELRDLL | SKIN | 765 | p.S765F | c.2294C>T | Missense_Mutation | 1 | 0.11 | MELJUSO | Y | 19 | 9 | 0 | N |
RET | FPVSYYSSG | LUNG | 683 | p.S688Y | c.2063C>A | Missense_Mutation | 1 | 0.11 | HARA | N | 3 | 0 | 0 | N |
RET | FQGPGAVVL | LUNG | 381 | p.G387V | c.1160G>T | Missense_Mutation | 1 | 0.11 | HARA | Y | 14 | 13 | 4 | N |
RET | FSTCSPITK | LARGE_INTESTINE | 555 | p.S561I | c.1682G>T | Missense_Mutation | 1 | 0.11 | T84 | N | 4 | 0 | 2 | N |
RET | GAHRPSLDS | OVARY | 691 | p.R693H | c.2078G>A | Missense_Mutation | 1 | 0.11 | JHOM2B | N | 1 | 0 | 0 | N |
RET | GARRASLDS | ENDOMETRIUM | 691 | p.P695A | c.2083C>G | Missense_Mutation | 1 | 0.11 | EN | N | 1 | 0 | 0 | N |
RET | GAVVLLLHF | LUNG | 385 | p.G387V | c.1160G>T | Missense_Mutation | 1 | 0.11 | HARA | N | 7 | 0 | 0 | N |
RET | GDLITFAWQ | LUNG | 849 | p.S853T | c.2557T>A | Missense_Mutation | 1 | 0.11 | NCIH2066 | N | 0 | 0 | 0 | N |
RET | GKVCVKNCQ | LUNG | 423 | p.E428K | c.1282G>A | Missense_Mutation | 1 | 0.11 | NCIH1339 | N | 0 | 0 | 0 | N |
RET | GLSEEEAPL | LARGE_INTESTINE | 1032 | p.T1038A | c.3112A>G | Missense_Mutation | 1 | 0.11 | SNU175 | N | 11 | 0 | 0 | N |
RET | GPGAVVLLL | LUNG | 383 | p.G387V | c.1160G>T | Missense_Mutation | 1 | 0.11 | HARA | Y | 17 | 11 | 0 | N |
RET | GPGYLRSGG | LUNG | 823 | p.G828R | c.2482G>C | Missense_Mutation | 1 | 0.11 | NCIH1105 | N | 0 | 0 | 0 | Y |
RET | GQHLYGTYL | LUNG | 69 | p.R77L | c.230G>T | Missense_Mutation | 1 | 0.11 | NCIH23 | Y | 11 | 11 | 0 | N |
RET | GRTGYTTVA | OVARY | 748 | p.A750T | c.2248G>A | Missense_Mutation | 1 | 0.11 | IGROV1 | N | 2 | 0 | 0 | N |
RET | GTFHQFHLL | LARGE_INTESTINE | 183 | p.R189H | c.566G>A | Missense_Mutation | 1 | 0.11 | T84 | Y | 15 | 10 | 0 | N |
RET | GTYLTRLHE | LUNG | 74 | p.R77L | c.230G>T | Missense_Mutation | 1 | 0.11 | NCIH23 | N | 0 | 0 | 0 | N |
RET | GYLRSGGSR | LUNG | 825 | p.G828R | c.2482G>C | Missense_Mutation | 1 | 0.11 | NCIH1105 | N | 3 | 0 | 0 | N |
RET | HDYRLVLNW | LARGE_INTESTINE | 352 | p.R360W | c.1078C>T | Missense_Mutation | 1 | 0.11 | SW48 | N | 6 | 0 | 0 | N |
RET | HLKGRTGYT | OVARY | 745 | p.A750T | c.2248G>A | Missense_Mutation | 1 | 0.11 | IGROV1 | N | 2 | 0 | 0 | N |
RET | HLLPVQFLC | LARGE_INTESTINE | 189 | p.R189H | c.566G>A | Missense_Mutation | 1 | 0.11 | T84 | Y | 4 | 11 | 0 | N |
RET | HLYGTYLTR | LUNG | 71 | p.R77L | c.230G>T | Missense_Mutation | 1 | 0.11 | NCIH23 | Y | 8 | 11 | 0 | N |
RET | HMKGRAGYT | PROSTATE | 745 | p.L746M | c.2236C>A | Missense_Mutation | 1 | 0.11 | DU145 | N | 1 | 0 | 0 | N |
RET | HPDEWALTM | LARGE_INTESTINE | 840 | p.R844W | c.2530C>T | Missense_Mutation | 1 | 0.11 | SNUC2A | Y | 13 | 9 | 0 | N |
RET | HPHVIKLNG | LUNG | 784 | p.Y791N | c.2371T>A | Missense_Mutation | 1 | 0.11 | NCIH1092 | N | 1 | 0 | 0 | Y |
RET | HQFHLLPVQ | LARGE_INTESTINE | 186 | p.R189H | c.566G>A | Missense_Mutation | 1 | 0.11 | T84 | N | 1 | 0 | 0 | N |
RET | HRPSLDSME | OVARY | 693 | p.R693H | c.2078G>A | Missense_Mutation | 1 | 0.11 | JHOM2B | N | 1 | 0 | 0 | N |
RET | HVIKLNGAC | LUNG | 786 | p.Y791N | c.2371T>A | Missense_Mutation | 1 | 0.11 | NCIH1092 | N | 0 | 0 | 0 | N |
RET | IAATVLFSF | OVARY | 638 | p.A641T | c.1921G>A | Missense_Mutation | 1 | 0.11 | OVK18 | N | 8 | 0 | 0 | N |
RET | IGKVCVKNC | LUNG | 422 | p.E428K | c.1282G>A | Missense_Mutation | 1 | 0.11 | NCIH1339 | N | 1 | 0 | 0 | N |
RET | IKLNGACSQ | LUNG | 788 | p.Y791N | c.2371T>A | Missense_Mutation | 1 | 0.11 | NCIH1092 | N | 0 | 0 | 28 | N |
RET | INKDLEKMM | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 1001 | p.S1002N | c.3005G>A | Missense_Mutation | 1 | 0.11 | DND41 | N | 3 | 0 | 0 | N |
RET | ISFAWQTSQ | PROSTATE | 852 | p.I858T | c.2573T>C | Missense_Mutation | 1 | 0.11 | LNCAPCLONEFGC | N | 0 | 0 | 0 | N |
RET | ITFAWQISQ | LUNG | 852 | p.S853T | c.2557T>A | Missense_Mutation | 1 | 0.11 | NCIH2066 | N | 0 | 0 | 0 | N |
RET | ITKTCPDGH | LARGE_INTESTINE | 561 | p.S561I | c.1682G>T | Missense_Mutation | 1 | 0.11 | T84 | N | 0 | 0 | 0 | N |
RET | KATAFHMKG | PROSTATE | 740 | p.L746M | c.2236C>A | Missense_Mutation | 1 | 0.11 | DU145 | N | 0 | 0 | 0 | N |
RET | KCAKLHYMV | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 477 | p.E480K | c.1438G>A | Missense_Mutation | 1 | 0.11 | HS611T | N | 4 | 0 | 0 | N |
RET | KENAFPSEL | SKIN | 761 | p.S765F | c.2294C>T | Missense_Mutation | 1 | 0.11 | MELJUSO | Y | 13 | 11 | 0 | N |
RET | KGRTGYTTV | OVARY | 747 | p.A750T | c.2248G>A | Missense_Mutation | 1 | 0.11 | IGROV1 | N | 5 | 0 | 0 | N |
RET | KLHYMVVAT | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 480 | p.E480K | c.1438G>A | Missense_Mutation | 1 | 0.11 | HS611T | N | 5 | 0 | 0 | N |
RET | KLNGACSQD | LUNG | 789 | p.Y791N | c.2371T>A | Missense_Mutation | 1 | 0.11 | NCIH1092 | N | 0 | 0 | 0 | N |
RET | KLYVDQTAG | LARGE_INTESTINE | 39 | p.A45T | c.133G>A | Missense_Mutation | 1 | 0.11 | CW2 | N | 0 | 0 | 0 | N |
RET | KMLKENAFP | SKIN | 758 | p.S765F | c.2294C>T | Missense_Mutation | 1 | 0.11 | MELJUSO | N | 1 | 0 | 0 | N |
RET | KNCQAFSGI | LUNG | 428 | p.E428K | c.1282G>A | Missense_Mutation | 1 | 0.11 | NCIH1339 | N | 3 | 0 | 0 | N |
RET | KPDKRPVFA | LARGE_INTESTINE | 991 | p.E991K | c.2971G>A | Missense_Mutation | 1 | 0.11 | SKCO1 | N | 7 | 0 | 0 | Y |
RET | KQKPDKRPV | LARGE_INTESTINE | 989 | p.E991K | c.2971G>A | Missense_Mutation | 1 | 0.11 | SKCO1 | N | 5 | 0 | 0 | Y |
RET | KRPVFADIN | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 994 | p.S1002N | c.3005G>A | Missense_Mutation | 1 | 0.11 | DND41 | N | 3 | 0 | 0 | N |
RET | KRRDYLELA | LUNG | 1011 | p.D1017E | c.3051C>G | Missense_Mutation | 1 | 0.11 | HARA | N | 3 | 0 | 0 | N |
RET | KVCVKNCQA | LUNG | 424 | p.E428K | c.1282G>A | Missense_Mutation | 1 | 0.11 | NCIH1339 | N | 3 | 0 | 0 | N |
RET | KVGPGYLRS | LUNG | 821 | p.G828R | c.2482G>C | Missense_Mutation | 1 | 0.11 | NCIH1105 | N | 1 | 0 | 0 | N |
RET | LCDELCRTM | CENTRAL_NERVOUS_SYSTEM | 629 | p.V637M | c.1909G>A | Missense_Mutation | 1 | 0.11 | KNS42 | N | 1 | 0 | 0 | N |
RET | LCDELWRTV | THYROID | 629 | p.C634W | c.1902C>G | Missense_Mutation | 1 | 0.11 | TT | N | 3 | 0 | 0 | N |
RET | LCRTMIAAA | CENTRAL_NERVOUS_SYSTEM | 633 | p.V637M | c.1909G>A | Missense_Mutation | 1 | 0.11 | KNS42 | N | 4 | 0 | 0 | N |
RET | LCRTVIAAT | OVARY | 633 | p.A641T | c.1921G>A | Missense_Mutation | 1 | 0.11 | OVK18 | N | 1 | 0 | 0 | N |
RET | LDHPDEWAL | LARGE_INTESTINE | 838 | p.R844W | c.2530C>T | Missense_Mutation | 1 | 0.11 | SNUC2A | N | 7 | 0 | 0 | Y |
RET | LELAASTPS | LUNG | 1016 | p.D1017E | c.3051C>G | Missense_Mutation | 1 | 0.11 | HARA | N | 4 | 0 | 8 | N |
RET | LISFAWQTS | PROSTATE | 851 | p.I858T | c.2573T>C | Missense_Mutation | 1 | 0.11 | LNCAPCLONEFGC | N | 0 | 0 | 3 | N |
RET | LITFAWQIS | LUNG | 851 | p.S853T | c.2557T>A | Missense_Mutation | 1 | 0.11 | NCIH2066 | N | 0 | 0 | 1 | N |
RET | LKENAFPSE | SKIN | 760 | p.S765F | c.2294C>T | Missense_Mutation | 1 | 0.11 | MELJUSO | N | 0 | 0 | 0 | N |
RET | LKGRTGYTT | OVARY | 746 | p.A750T | c.2248G>A | Missense_Mutation | 1 | 0.11 | IGROV1 | N | 1 | 0 | 0 | N |
RET | LLVTVEESY | UPPER_AERODIGESTIVE_TRACT | 500 | p.G506E | c.1517G>A | Missense_Mutation | 1 | 0.11 | SNU1076 | N | 7 | 0 | 0 | N |
RET | LMLQCWKQK | LARGE_INTESTINE | 983 | p.E991K | c.2971G>A | Missense_Mutation | 1 | 0.11 | SKCO1 | N | 4 | 0 | 2 | N |
RET | LNGACSQDG | LUNG | 790 | p.Y791N | c.2371T>A | Missense_Mutation | 1 | 0.11 | NCIH1092 | N | 0 | 0 | 1 | N |
RET | LNWNLSISE | LARGE_INTESTINE | 358 | p.R360W | c.1078C>T | Missense_Mutation | 1 | 0.11 | SW48 | N | 0 | 0 | 0 | N |
RET | LPVCLHLPS | SKIN | 398 | p.S401C | c.1201A>T | Missense_Mutation | 1 | 0.11 | RPMI7951 | N | 8 | 0 | 4 | N |
RET | LQCWKQKPD | LARGE_INTESTINE | 985 | p.E991K | c.2971G>A | Missense_Mutation | 1 | 0.11 | SKCO1 | N | 0 | 0 | 1 | N |
RET | LRRPKCAKL | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 473 | p.E480K | c.1438G>A | Missense_Mutation | 1 | 0.11 | HS611T | Y | 7 | 9 | 5 | N |
RET | LRSGGSRNS | LUNG | 827 | p.G828R | c.2482G>C | Missense_Mutation | 1 | 0.11 | NCIH1105 | N | 2 | 0 | 19 | N |
RET | LSEEEAPLV | LARGE_INTESTINE | 1033 | p.T1038A | c.3112A>G | Missense_Mutation | 1 | 0.11 | SNU175 | N | 3 | 0 | 0 | N |
RET | LSPSVAKLM | LUNG | 1101 | p.A1105V | c.3314C>T | Missense_Mutation | 1 | 0.11 | NCIH1092 | N | 10 | 0 | 0 | N |
RET | LTMGDLITF | LUNG | 846 | p.S853T | c.2557T>A | Missense_Mutation | 1 | 0.11 | NCIH2066 | N | 9 | 0 | 2 | N |
RET | LTRLHENNW | LUNG | 77 | p.R77L | c.230G>T | Missense_Mutation | 1 | 0.11 | NCIH23 | N | 2 | 0 | 0 | N |
RET | LVDCNNAPF | ENDOMETRIUM | 1040 | p.L1048F | c.3142C>T | Missense_Mutation | 1 | 0.11 | TEN | N | 4 | 0 | 0 | N |
RET | LVLNWNLSI | LARGE_INTESTINE | 356 | p.R360W | c.1078C>T | Missense_Mutation | 1 | 0.11 | SW48 | N | 13 | 0 | 44 | Y |
RET | LVRRYTSTV | LUNG | 310 | p.L318V | c.952C>G | Missense_Mutation | 1 | 0.11 | NCIH1563 | N | 5 | 0 | 20 | N |
RET | LVTVEESYV | UPPER_AERODIGESTIVE_TRACT | 501 | p.G506E | c.1517G>A | Missense_Mutation | 1 | 0.11 | SNU1076 | N | 5 | 0 | 0 | N |
RET | LWRTVIAAA | THYROID | 633 | p.C634W | c.1902C>G | Missense_Mutation | 1 | 0.11 | TT | N | 3 | 0 | 0 | N |
RET | LYGTYLTRL | LUNG | 72 | p.R77L | c.230G>T | Missense_Mutation | 1 | 0.11 | NCIH23 | Y | 9 | 10 | 2 | N |
RET | LYVDQTAGT | LARGE_INTESTINE | 40 | p.A45T | c.133G>A | Missense_Mutation | 1 | 0.11 | CW2 | N | 3 | 0 | 11 | N |
RET | MGDLITFAW | LUNG | 848 | p.S853T | c.2557T>A | Missense_Mutation | 1 | 0.11 | NCIH2066 | N | 4 | 0 | 0 | N |
RET | MIAAAVLFS | CENTRAL_NERVOUS_SYSTEM | 637 | p.V637M | c.1909G>A | Missense_Mutation | 1 | 0.11 | KNS42 | N | 0 | 0 | 41 | N |
RET | MKGRAGYTT | PROSTATE | 746 | p.L746M | c.2236C>A | Missense_Mutation | 1 | 0.11 | DU145 | N | 1 | 0 | 0 | N |
RET | MLKENAFPS | SKIN | 759 | p.S765F | c.2294C>T | Missense_Mutation | 1 | 0.11 | MELJUSO | N | 0 | 0 | 0 | N |
RET | MLQCWKQKP | LARGE_INTESTINE | 984 | p.E991K | c.2971G>A | Missense_Mutation | 1 | 0.11 | SKCO1 | N | 1 | 0 | 0 | N |
RET | MLSPSVAKL | LUNG | 1100 | p.A1105V | c.3314C>T | Missense_Mutation | 1 | 0.11 | NCIH1092 | Y | 12 | 12 | 0 | N |
RET | MVKRRDYLE | LUNG | 1009 | p.D1017E | c.3051C>G | Missense_Mutation | 1 | 0.11 | HARA | N | 0 | 0 | 0 | N |
RET | NAFPSELRD | SKIN | 763 | p.S765F | c.2294C>T | Missense_Mutation | 1 | 0.11 | MELJUSO | N | 0 | 0 | 0 | N |
RET | NAPFPRALP | ENDOMETRIUM | 1045 | p.L1048F | c.3142C>T | Missense_Mutation | 1 | 0.11 | TEN | N | 0 | 0 | 0 | N |
RET | NFSTCSPIT | LARGE_INTESTINE | 554 | p.S561I | c.1682G>T | Missense_Mutation | 1 | 0.11 | T84 | N | 1 | 0 | 0 | N |
RET | NGACSQDGP | LUNG | 791 | p.Y791N | c.2371T>A | Missense_Mutation | 1 | 0.11 | NCIH1092 | N | 0 | 0 | 0 | N |
RET | NHPHVIKLN | LUNG | 783 | p.Y791N | c.2371T>A | Missense_Mutation | 1 | 0.11 | NCIH1092 | N | 1 | 0 | 0 | N |
RET | NKDLEKMMV | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 1002 | p.S1002N | c.3005G>A | Missense_Mutation | 1 | 0.11 | DND41 | N | 1 | 0 | 0 | N |
RET | NNAPFPRAL | ENDOMETRIUM | 1044 | p.L1048F | c.3142C>T | Missense_Mutation | 1 | 0.11 | TEN | Y | 7 | 14 | 0 | N |
RET | NVSVLPVCL | SKIN | 394 | p.S401C | c.1201A>T | Missense_Mutation | 1 | 0.11 | RPMI7951 | N | 5 | 0 | 0 | N |
RET | NWMLSPSVA | LUNG | 1098 | p.A1105V | c.3314C>T | Missense_Mutation | 1 | 0.11 | NCIH1092 | N | 0 | 0 | 0 | N |
RET | NWNLSISEN | LARGE_INTESTINE | 359 | p.R360W | c.1078C>T | Missense_Mutation | 1 | 0.11 | SW48 | N | 0 | 0 | 0 | N |
RET | PDEWALTMG | LARGE_INTESTINE | 841 | p.R844W | c.2530C>T | Missense_Mutation | 1 | 0.11 | SNUC2A | N | 0 | 0 | 0 | N |
RET | PFPRALPST | ENDOMETRIUM | 1047 | p.L1048F | c.3142C>T | Missense_Mutation | 1 | 0.11 | TEN | N | 0 | 0 | 0 | N |
RET | PGAVVLLLH | LUNG | 384 | p.G387V | c.1160G>T | Missense_Mutation | 1 | 0.11 | HARA | N | 0 | 0 | 0 | N |
RET | PGTFHQFHL | LARGE_INTESTINE | 182 | p.R189H | c.566G>A | Missense_Mutation | 1 | 0.11 | T84 | N | 0 | 0 | 0 | N |
RET | PGYLRSGGS | LUNG | 824 | p.G828R | c.2482G>C | Missense_Mutation | 1 | 0.11 | NCIH1105 | N | 0 | 0 | 0 | Y |
RET | PHVIKLNGA | LUNG | 785 | p.Y791N | c.2371T>A | Missense_Mutation | 1 | 0.11 | NCIH1092 | N | 0 | 0 | 0 | N |
RET | PITKTCPDG | LARGE_INTESTINE | 560 | p.S561I | c.1682G>T | Missense_Mutation | 1 | 0.11 | T84 | N | 0 | 0 | 0 | N |
RET | PKCAKLHYM | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 476 | p.E480K | c.1438G>A | Missense_Mutation | 1 | 0.11 | HS611T | N | 2 | 0 | 0 | N |
RET | PLCDELWRT | THYROID | 628 | p.C634W | c.1902C>G | Missense_Mutation | 1 | 0.11 | TT | N | 1 | 0 | 0 | N |
RET | PPGTFHQFH | LARGE_INTESTINE | 181 | p.R189H | c.566G>A | Missense_Mutation | 1 | 0.11 | T84 | N | 0 | 0 | 0 | N |
RET | PSVAKLMDT | LUNG | 1103 | p.A1105V | c.3314C>T | Missense_Mutation | 1 | 0.11 | NCIH1092 | N | 0 | 0 | 0 | N |
RET | PVCLHLPST | SKIN | 399 | p.S401C | c.1201A>T | Missense_Mutation | 1 | 0.11 | RPMI7951 | N | 0 | 0 | 0 | N |
RET | PVFADINKD | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 996 | p.S1002N | c.3005G>A | Missense_Mutation | 1 | 0.11 | DND41 | N | 0 | 0 | 0 | Y |
RET | PVSYYSSGA | LUNG | 684 | p.S688Y | c.2063C>A | Missense_Mutation | 1 | 0.11 | HARA | N | 1 | 0 | 0 | N |
RET | QAFPVSYYS | LUNG | 681 | p.S688Y | c.2063C>A | Missense_Mutation | 1 | 0.11 | HARA | N | 3 | 0 | 0 | N |
RET | QCWKQKPDK | LARGE_INTESTINE | 986 | p.E991K | c.2971G>A | Missense_Mutation | 1 | 0.11 | SKCO1 | N | 2 | 0 | 0 | N |
RET | QDPLCDELW | THYROID | 626 | p.C634W | c.1902C>G | Missense_Mutation | 1 | 0.11 | TT | N | 3 | 0 | 0 | N |
RET | QFHLLPVQF | LARGE_INTESTINE | 187 | p.R189H | c.566G>A | Missense_Mutation | 1 | 0.11 | T84 | N | 4 | 0 | 0 | N |
RET | QGPGAVVLL | LUNG | 382 | p.G387V | c.1160G>T | Missense_Mutation | 1 | 0.11 | HARA | Y | 13 | 9 | 0 | N |
RET | QHLYGTYLT | LUNG | 70 | p.R77L | c.230G>T | Missense_Mutation | 1 | 0.11 | NCIH23 | N | 1 | 0 | 0 | N |
RET | QIGKVCVKN | LUNG | 421 | p.E428K | c.1282G>A | Missense_Mutation | 1 | 0.11 | NCIH1339 | N | 0 | 0 | 0 | N |
RET | QKPDKRPVF | LARGE_INTESTINE | 990 | p.E991K | c.2971G>A | Missense_Mutation | 1 | 0.11 | SKCO1 | N | 3 | 0 | 0 | N |
RET | QLLVTVEES | UPPER_AERODIGESTIVE_TRACT | 499 | p.G506E | c.1517G>A | Missense_Mutation | 1 | 0.11 | SNU1076 | N | 0 | 0 | 0 | N |
RET | QTAGTPLLY | LARGE_INTESTINE | 44 | p.A45T | c.133G>A | Missense_Mutation | 1 | 0.11 | CW2 | N | 7 | 0 | 0 | N |
RET | QTSQGMQYL | PROSTATE | 857 | p.I858T | c.2573T>C | Missense_Mutation | 1 | 0.11 | LNCAPCLONEFGC | Y | 5 | 9 | 0 | N |
RET | RASLDSMEN | ENDOMETRIUM | 694 | p.P695A | c.2083C>G | Missense_Mutation | 1 | 0.11 | EN | N | 1 | 0 | 0 | N |
RET | RDYLELAAS | LUNG | 1013 | p.D1017E | c.3051C>G | Missense_Mutation | 1 | 0.11 | HARA | N | 1 | 0 | 0 | N |
RET | RKVGPGYLR | LUNG | 820 | p.G828R | c.2482G>C | Missense_Mutation | 1 | 0.11 | NCIH1105 | N | 2 | 0 | 0 | N |
RET | RLVLNWNLS | LARGE_INTESTINE | 355 | p.R360W | c.1078C>T | Missense_Mutation | 1 | 0.11 | SW48 | N | 1 | 0 | 0 | Y |
RET | RNFSTCSPI | LARGE_INTESTINE | 553 | p.S561I | c.1682G>T | Missense_Mutation | 1 | 0.11 | T84 | N | 7 | 0 | 0 | N |
RET | RPKCAKLHY | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 475 | p.E480K | c.1438G>A | Missense_Mutation | 1 | 0.11 | HS611T | Y | 12 | 11 | 0 | N |
RET | RPVFADINK | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 995 | p.S1002N | c.3005G>A | Missense_Mutation | 1 | 0.11 | DND41 | Y | 6 | 11 | 0 | N |
RET | RRASLDSME | ENDOMETRIUM | 693 | p.P695A | c.2083C>G | Missense_Mutation | 1 | 0.11 | EN | N | 2 | 0 | 0 | N |
RET | RRDYLELAA | LUNG | 1012 | p.D1017E | c.3051C>G | Missense_Mutation | 1 | 0.11 | HARA | N | 3 | 0 | 0 | N |
RET | RRPKCAKLH | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 474 | p.E480K | c.1438G>A | Missense_Mutation | 1 | 0.11 | HS611T | N | 2 | 0 | 0 | N |
RET | RRYTSTVLP | LUNG | 312 | p.L318V | c.952C>G | Missense_Mutation | 1 | 0.11 | NCIH1563 | N | 2 | 0 | 0 | N |
RET | RSGGSRNSS | LUNG | 828 | p.G828R | c.2482G>C | Missense_Mutation | 1 | 0.11 | NCIH1105 | N | 1 | 0 | 0 | N |
RET | RTGYTTVAV | OVARY | 749 | p.A750T | c.2248G>A | Missense_Mutation | 1 | 0.11 | IGROV1 | Y | 3 | 13 | 0 | N |
RET | RTMIAAAVL | CENTRAL_NERVOUS_SYSTEM | 635 | p.V637M | c.1909G>A | Missense_Mutation | 1 | 0.11 | KNS42 | N | 13 | 0 | 0 | N |
RET | RTVIAATVL | OVARY | 635 | p.A641T | c.1921G>A | Missense_Mutation | 1 | 0.11 | OVK18 | N | 13 | 0 | 0 | N |
RET | RYTSTVLPG | LUNG | 313 | p.L318V | c.952C>G | Missense_Mutation | 1 | 0.11 | NCIH1563 | N | 1 | 0 | 0 | N |
RET | SAAKLMDTY | URINARY_TRACT | 1104 | p.F1112Y | c.3335T>A | Missense_Mutation | 1 | 0.11 | J82 | N | 5 | 0 | 0 | N |
RET | SDFQGPGAV | LUNG | 379 | p.G387V | c.1160G>T | Missense_Mutation | 1 | 0.11 | HARA | N | 6 | 0 | 0 | N |
RET | SEEEAPLVD | LARGE_INTESTINE | 1034 | p.T1038A | c.3112A>G | Missense_Mutation | 1 | 0.11 | SNU175 | N | 0 | 0 | 0 | N |
RET | SFAWQTSQG | PROSTATE | 853 | p.I858T | c.2573T>C | Missense_Mutation | 1 | 0.11 | LNCAPCLONEFGC | N | 0 | 0 | 0 | N |
RET | SGAHRPSLD | OVARY | 690 | p.R693H | c.2078G>A | Missense_Mutation | 1 | 0.11 | JHOM2B | N | 0 | 0 | 0 | N |
RET | SGARRASLD | ENDOMETRIUM | 690 | p.P695A | c.2083C>G | Missense_Mutation | 1 | 0.11 | EN | N | 0 | 0 | 0 | N |
RET | SLDHPDEWA | LARGE_INTESTINE | 837 | p.R844W | c.2530C>T | Missense_Mutation | 1 | 0.11 | SNUC2A | N | 2 | 0 | 0 | N |
RET | SPITKTCPD | LARGE_INTESTINE | 559 | p.S561I | c.1682G>T | Missense_Mutation | 1 | 0.11 | T84 | N | 1 | 0 | 0 | N |
RET | SPSVAKLMD | LUNG | 1102 | p.A1105V | c.3314C>T | Missense_Mutation | 1 | 0.11 | NCIH1092 | N | 0 | 0 | 0 | N |
RET | SSGAHRPSL | OVARY | 689 | p.R693H | c.2078G>A | Missense_Mutation | 1 | 0.11 | JHOM2B | N | 8 | 0 | 0 | Y |
RET | SSGARRASL | ENDOMETRIUM | 689 | p.P695A | c.2083C>G | Missense_Mutation | 1 | 0.11 | EN | Y | 10 | 12 | 0 | N |
RET | SSLDHPDEW | LARGE_INTESTINE | 836 | p.R844W | c.2530C>T | Missense_Mutation | 1 | 0.11 | SNUC2A | N | 3 | 0 | 0 | N |
RET | SSSGAHRPS | OVARY | 688 | p.R693H | c.2078G>A | Missense_Mutation | 1 | 0.11 | JHOM2B | N | 0 | 0 | 0 | Y |
RET | SSSGARRAS | ENDOMETRIUM | 688 | p.P695A | c.2083C>G | Missense_Mutation | 1 | 0.11 | EN | N | 0 | 0 | 0 | N |
RET | STCSPITKT | LARGE_INTESTINE | 556 | p.S561I | c.1682G>T | Missense_Mutation | 1 | 0.11 | T84 | N | 1 | 0 | 0 | N |
RET | STVLPGDTW | LUNG | 316 | p.L318V | c.952C>G | Missense_Mutation | 1 | 0.11 | NCIH1563 | N | 2 | 0 | 0 | N |
RET | SVAKLMDTF | LUNG | 1104 | p.A1105V | c.3314C>T | Missense_Mutation | 1 | 0.11 | NCIH1092 | N | 4 | 0 | 0 | N |
RET | SVLPVCLHL | SKIN | 396 | p.S401C | c.1201A>T | Missense_Mutation | 1 | 0.11 | RPMI7951 | Y | 14 | 9 | 0 | N |
RET | SYSSSGAHR | OVARY | 686 | p.R693H | c.2078G>A | Missense_Mutation | 1 | 0.11 | JHOM2B | Y | 2 | 10 | 0 | N |
RET | SYYSSGARR | LUNG | 686 | p.S688Y | c.2063C>A | Missense_Mutation | 1 | 0.11 | HARA | Y | 3 | 11 | 0 | N |
RET | TAFHLKGRT | OVARY | 742 | p.A750T | c.2248G>A | Missense_Mutation | 1 | 0.11 | IGROV1 | N | 4 | 0 | 0 | N |
RET | TAFHMKGRA | PROSTATE | 742 | p.L746M | c.2236C>A | Missense_Mutation | 1 | 0.11 | DU145 | N | 7 | 0 | 0 | N |
RET | TAGTPLLYV | LARGE_INTESTINE | 45 | p.A45T | c.133G>A | Missense_Mutation | 1 | 0.11 | CW2 | Y | 6 | 9 | 0 | N |
RET | TCSPITKTC | LARGE_INTESTINE | 557 | p.S561I | c.1682G>T | Missense_Mutation | 1 | 0.11 | T84 | N | 0 | 0 | 0 | N |
RET | TFAWQISQG | LUNG | 853 | p.S853T | c.2557T>A | Missense_Mutation | 1 | 0.11 | NCIH2066 | N | 0 | 0 | 0 | N |
RET | TFHQFHLLP | LARGE_INTESTINE | 184 | p.R189H | c.566G>A | Missense_Mutation | 1 | 0.11 | T84 | N | 0 | 0 | 0 | N |
RET | TGYTTVAVK | OVARY | 750 | p.A750T | c.2248G>A | Missense_Mutation | 1 | 0.11 | IGROV1 | N | 1 | 0 | 0 | N |
RET | TMGDLITFA | LUNG | 847 | p.S853T | c.2557T>A | Missense_Mutation | 1 | 0.11 | NCIH2066 | N | 2 | 0 | 0 | N |
RET | TMIAAAVLF | CENTRAL_NERVOUS_SYSTEM | 636 | p.V637M | c.1909G>A | Missense_Mutation | 1 | 0.11 | KNS42 | N | 5 | 0 | 0 | N |
RET | TSQGMQYLA | PROSTATE | 858 | p.I858T | c.2573T>C | Missense_Mutation | 1 | 0.11 | LNCAPCLONEFGC | N | 1 | 0 | 0 | N |
RET | TSTVLPGDT | LUNG | 315 | p.L318V | c.952C>G | Missense_Mutation | 1 | 0.11 | NCIH1563 | N | 1 | 0 | 0 | N |
RET | TVEESYVAE | UPPER_AERODIGESTIVE_TRACT | 503 | p.G506E | c.1517G>A | Missense_Mutation | 1 | 0.11 | SNU1076 | N | 0 | 0 | 0 | Y |
RET | TVIAATVLF | OVARY | 636 | p.A641T | c.1921G>A | Missense_Mutation | 1 | 0.11 | OVK18 | N | 2 | 0 | 0 | N |
RET | TVLFSFIVS | OVARY | 641 | p.A641T | c.1921G>A | Missense_Mutation | 1 | 0.11 | OVK18 | N | 0 | 0 | 0 | N |
RET | TVLPGDTWA | LUNG | 317 | p.L318V | c.952C>G | Missense_Mutation | 1 | 0.11 | NCIH1563 | N | 3 | 0 | 0 | N |
RET | TYLTRLHEN | LUNG | 75 | p.R77L | c.230G>T | Missense_Mutation | 1 | 0.11 | NCIH23 | N | 2 | 0 | 0 | N |
RET | VAKLMDTFD | LUNG | 1105 | p.A1105V | c.3314C>T | Missense_Mutation | 1 | 0.11 | NCIH1092 | N | 0 | 0 | 0 | N |
RET | VCLHLPSTY | SKIN | 400 | p.S401C | c.1201A>T | Missense_Mutation | 1 | 0.11 | RPMI7951 | N | 6 | 0 | 0 | N |
RET | VCVKNCQAF | LUNG | 425 | p.E428K | c.1282G>A | Missense_Mutation | 1 | 0.11 | NCIH1339 | N | 6 | 0 | 0 | N |
RET | VDCNNAPFP | ENDOMETRIUM | 1041 | p.L1048F | c.3142C>T | Missense_Mutation | 1 | 0.11 | TEN | N | 1 | 0 | 0 | N |
RET | VDQTAGTPL | LARGE_INTESTINE | 42 | p.A45T | c.133G>A | Missense_Mutation | 1 | 0.11 | CW2 | N | 8 | 0 | 0 | N |
RET | VEESYVAEE | UPPER_AERODIGESTIVE_TRACT | 504 | p.G506E | c.1517G>A | Missense_Mutation | 1 | 0.11 | SNU1076 | N | 0 | 0 | 0 | Y |
RET | VFADINKDL | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 997 | p.S1002N | c.3005G>A | Missense_Mutation | 1 | 0.11 | DND41 | N | 9 | 0 | 0 | Y |
RET | VGPGYLRSG | LUNG | 822 | p.G828R | c.2482G>C | Missense_Mutation | 1 | 0.11 | NCIH1105 | N | 1 | 0 | 0 | N |
RET | VIAATVLFS | OVARY | 637 | p.A641T | c.1921G>A | Missense_Mutation | 1 | 0.11 | OVK18 | N | 0 | 0 | 41 | N |
RET | VIKLNGACS | LUNG | 787 | p.Y791N | c.2371T>A | Missense_Mutation | 1 | 0.11 | NCIH1092 | N | 0 | 0 | 8 | N |
RET | VKATAFHMK | PROSTATE | 739 | p.L746M | c.2236C>A | Missense_Mutation | 1 | 0.11 | DU145 | N | 1 | 0 | 2 | N |
RET | VKMLKENAF | SKIN | 757 | p.S765F | c.2294C>T | Missense_Mutation | 1 | 0.11 | MELJUSO | N | 3 | 0 | 1 | N |
RET | VKNCQAFSG | LUNG | 427 | p.E428K | c.1282G>A | Missense_Mutation | 1 | 0.11 | NCIH1339 | N | 0 | 0 | 6 | N |
RET | VKRRDYLEL | LUNG | 1010 | p.D1017E | c.3051C>G | Missense_Mutation | 1 | 0.11 | HARA | N | 4 | 0 | 7 | Y |
RET | VLNWNLSIS | LARGE_INTESTINE | 357 | p.R360W | c.1078C>T | Missense_Mutation | 1 | 0.11 | SW48 | N | 0 | 0 | 8 | N |
RET | VLPGDTWAQ | LUNG | 318 | p.L318V | c.952C>G | Missense_Mutation | 1 | 0.11 | NCIH1563 | N | 0 | 0 | 2 | N |
RET | VLPVCLHLP | SKIN | 397 | p.S401C | c.1201A>T | Missense_Mutation | 1 | 0.11 | RPMI7951 | N | 0 | 0 | 0 | N |
RET | VRRYTSTVL | LUNG | 311 | p.L318V | c.952C>G | Missense_Mutation | 1 | 0.11 | NCIH1563 | N | 5 | 0 | 18 | N |
RET | VSVLPVCLH | SKIN | 395 | p.S401C | c.1201A>T | Missense_Mutation | 1 | 0.11 | RPMI7951 | N | 0 | 0 | 18 | N |
RET | VSYSSSGAH | OVARY | 685 | p.R693H | c.2078G>A | Missense_Mutation | 1 | 0.11 | JHOM2B | N | 0 | 0 | 0 | N |
RET | VSYYSSGAR | LUNG | 685 | p.S688Y | c.2063C>A | Missense_Mutation | 1 | 0.11 | HARA | N | 4 | 0 | 0 | N |
RET | VTVEESYVA | UPPER_AERODIGESTIVE_TRACT | 502 | p.G506E | c.1517G>A | Missense_Mutation | 1 | 0.11 | SNU1076 | N | 5 | 0 | 0 | N |
RET | VVKATAFHM | PROSTATE | 738 | p.L746M | c.2236C>A | Missense_Mutation | 1 | 0.11 | DU145 | Y | 5 | 10 | 24 | N |
RET | VVLLLHFNV | LUNG | 387 | p.G387V | c.1160G>T | Missense_Mutation | 1 | 0.11 | HARA | Y | 8 | 10 | 38 | N |
RET | WALTMGDLI | LARGE_INTESTINE | 844 | p.R844W | c.2530C>T | Missense_Mutation | 1 | 0.11 | SNUC2A | N | 14 | 0 | 0 | Y |
RET | WEKLYVDQT | LARGE_INTESTINE | 37 | p.A45T | c.133G>A | Missense_Mutation | 1 | 0.11 | CW2 | N | 7 | 0 | 0 | N |
RET | WKQKPDKRP | LARGE_INTESTINE | 988 | p.E991K | c.2971G>A | Missense_Mutation | 1 | 0.11 | SKCO1 | N | 1 | 0 | 0 | Y |
RET | WMLSPSVAK | LUNG | 1099 | p.A1105V | c.3314C>T | Missense_Mutation | 1 | 0.11 | NCIH1092 | N | 9 | 0 | 10 | N |
RET | WNLSISENR | LARGE_INTESTINE | 360 | p.R360W | c.1078C>T | Missense_Mutation | 1 | 0.11 | SW48 | N | 4 | 0 | 7 | N |
RET | WQTSQGMQY | PROSTATE | 856 | p.I858T | c.2573T>C | Missense_Mutation | 1 | 0.11 | LNCAPCLONEFGC | N | 9 | 0 | 3 | N |
RET | WRTVIAAAV | THYROID | 634 | p.C634W | c.1902C>G | Missense_Mutation | 1 | 0.11 | TT | Y | 7 | 10 | 16 | N |
RET | YGTYLTRLH | LUNG | 73 | p.R77L | c.230G>T | Missense_Mutation | 1 | 0.11 | NCIH23 | N | 2 | 0 | 16 | N |
RET | YLELAASTP | LUNG | 1015 | p.D1017E | c.3051C>G | Missense_Mutation | 1 | 0.11 | HARA | N | 2 | 0 | 0 | N |
RET | YLRSGGSRN | LUNG | 826 | p.G828R | c.2482G>C | Missense_Mutation | 1 | 0.11 | NCIH1105 | N | 4 | 0 | 0 | N |
RET | YLTRLHENN | LUNG | 76 | p.R77L | c.230G>T | Missense_Mutation | 1 | 0.11 | NCIH23 | N | 1 | 0 | 0 | N |
RET | YRLVLNWNL | LARGE_INTESTINE | 354 | p.R360W | c.1078C>T | Missense_Mutation | 1 | 0.11 | SW48 | Y | 11 | 10 | 20 | Y |
RET | YSSGARRPS | LUNG | 688 | p.S688Y | c.2063C>A | Missense_Mutation | 1 | 0.11 | HARA | N | 1 | 0 | 2 | Y |
RET | YSSSGAHRP | OVARY | 687 | p.R693H | c.2078G>A | Missense_Mutation | 1 | 0.11 | JHOM2B | N | 2 | 0 | 0 | N |
RET | YSSSGARRA | ENDOMETRIUM | 687 | p.P695A | c.2083C>G | Missense_Mutation | 1 | 0.11 | EN | Y | 4 | 9 | 0 | N |
RET | YTSTVLPGD | LUNG | 314 | p.L318V | c.952C>G | Missense_Mutation | 1 | 0.11 | NCIH1563 | N | 2 | 0 | 0 | N |
RET | YVDQTAGTP | LARGE_INTESTINE | 41 | p.A45T | c.133G>A | Missense_Mutation | 1 | 0.11 | CW2 | N | 2 | 0 | 0 | N |
RET | YYSSGARRP | LUNG | 687 | p.S688Y | c.2063C>A | Missense_Mutation | 1 | 0.11 | HARA | N | 2 | 0 | 0 | N |
RET | CPNGHCDVV | LIVER | 565 | p.D567N | c.1699G>A | Missense_Mutation | 1 | 0.22 | C3A | N | 12 | 0 | 0 | N |
RET | CPNGHCDVV | LIVER | 565 | p.D567N | c.1699G>A | Missense_Mutation | 1 | 0.22 | HEPG2 | N | 12 | 0 | 0 | N |
RET | CSEETYRLM | LARGE_INTESTINE | 976 | p.M980T | c.2939T>C | Missense_Mutation | 1 | 0.22 | HCT15 | Y | 4 | 9 | 0 | N |
RET | CSEETYRLM | LARGE_INTESTINE | 976 | p.M980T | c.2939T>C | Missense_Mutation | 1 | 0.22 | HRT18 | Y | 4 | 9 | 0 | N |
RET | DNCSEETYR | LARGE_INTESTINE | 974 | p.M980T | c.2939T>C | Missense_Mutation | 1 | 0.22 | HCT15 | N | 2 | 0 | 0 | N |
RET | DNCSEETYR | LARGE_INTESTINE | 974 | p.M980T | c.2939T>C | Missense_Mutation | 1 | 0.22 | HRT18 | N | 2 | 0 | 0 | N |
RET | EETYRLMLQ | LARGE_INTESTINE | 978 | p.M980T | c.2939T>C | Missense_Mutation | 1 | 0.22 | HCT15 | N | 0 | 0 | 0 | N |
RET | EETYRLMLQ | LARGE_INTESTINE | 978 | p.M980T | c.2939T>C | Missense_Mutation | 1 | 0.22 | HRT18 | N | 0 | 0 | 0 | N |
RET | ETYRLMLQC | LARGE_INTESTINE | 979 | p.M980T | c.2939T>C | Missense_Mutation | 1 | 0.22 | HCT15 | N | 1 | 0 | 0 | N |
RET | ETYRLMLQC | LARGE_INTESTINE | 979 | p.M980T | c.2939T>C | Missense_Mutation | 1 | 0.22 | HRT18 | N | 1 | 0 | 0 | N |
RET | KTCPNGHCD | LIVER | 563 | p.D567N | c.1699G>A | Missense_Mutation | 1 | 0.22 | C3A | N | 2 | 0 | 0 | N |
RET | KTCPNGHCD | LIVER | 563 | p.D567N | c.1699G>A | Missense_Mutation | 1 | 0.22 | HEPG2 | N | 2 | 0 | 0 | N |
RET | NCSEETYRL | LARGE_INTESTINE | 975 | p.M980T | c.2939T>C | Missense_Mutation | 1 | 0.22 | HCT15 | N | 6 | 0 | 0 | N |
RET | NCSEETYRL | LARGE_INTESTINE | 975 | p.M980T | c.2939T>C | Missense_Mutation | 1 | 0.22 | HRT18 | N | 6 | 0 | 0 | N |
RET | NGHCDVVET | LIVER | 567 | p.D567N | c.1699G>A | Missense_Mutation | 1 | 0.22 | C3A | N | 1 | 0 | 0 | N |
RET | NGHCDVVET | LIVER | 567 | p.D567N | c.1699G>A | Missense_Mutation | 1 | 0.22 | HEPG2 | N | 1 | 0 | 0 | N |
RET | PDNCSEETY | LARGE_INTESTINE | 973 | p.M980T | c.2939T>C | Missense_Mutation | 1 | 0.22 | HCT15 | N | 1 | 0 | 0 | N |
RET | PDNCSEETY | LARGE_INTESTINE | 973 | p.M980T | c.2939T>C | Missense_Mutation | 1 | 0.22 | HRT18 | N | 1 | 0 | 0 | N |
RET | PNGHCDVVE | LIVER | 566 | p.D567N | c.1699G>A | Missense_Mutation | 1 | 0.22 | C3A | N | 0 | 0 | 0 | Y |
RET | PNGHCDVVE | LIVER | 566 | p.D567N | c.1699G>A | Missense_Mutation | 1 | 0.22 | HEPG2 | N | 0 | 0 | 0 | Y |
RET | PSTKTCPNG | LIVER | 560 | p.D567N | c.1699G>A | Missense_Mutation | 1 | 0.22 | C3A | N | 0 | 0 | 0 | Y |
RET | PSTKTCPNG | LIVER | 560 | p.D567N | c.1699G>A | Missense_Mutation | 1 | 0.22 | HEPG2 | N | 0 | 0 | 0 | Y |
RET | RPDNCSEET | LARGE_INTESTINE | 972 | p.M980T | c.2939T>C | Missense_Mutation | 1 | 0.22 | HCT15 | N | 3 | 0 | 0 | N |
RET | RPDNCSEET | LARGE_INTESTINE | 972 | p.M980T | c.2939T>C | Missense_Mutation | 1 | 0.22 | HRT18 | N | 3 | 0 | 0 | N |
RET | SEETYRLML | LARGE_INTESTINE | 977 | p.M980T | c.2939T>C | Missense_Mutation | 1 | 0.22 | HCT15 | Y | 8 | 10 | 0 | N |
RET | SEETYRLML | LARGE_INTESTINE | 977 | p.M980T | c.2939T>C | Missense_Mutation | 1 | 0.22 | HRT18 | Y | 8 | 10 | 0 | N |
RET | SPSTKTCPN | LIVER | 559 | p.D567N | c.1699G>A | Missense_Mutation | 1 | 0.22 | C3A | N | 3 | 0 | 0 | N |
RET | SPSTKTCPN | LIVER | 559 | p.D567N | c.1699G>A | Missense_Mutation | 1 | 0.22 | HEPG2 | N | 3 | 0 | 0 | N |
RET | STKTCPNGH | LIVER | 561 | p.D567N | c.1699G>A | Missense_Mutation | 1 | 0.22 | C3A | N | 0 | 0 | 0 | N |
RET | STKTCPNGH | LIVER | 561 | p.D567N | c.1699G>A | Missense_Mutation | 1 | 0.22 | HEPG2 | N | 0 | 0 | 0 | N |
RET | TCPNGHCDV | LIVER | 564 | p.D567N | c.1699G>A | Missense_Mutation | 1 | 0.22 | C3A | N | 2 | 0 | 0 | N |
RET | TCPNGHCDV | LIVER | 564 | p.D567N | c.1699G>A | Missense_Mutation | 1 | 0.22 | HEPG2 | N | 2 | 0 | 0 | N |
RET | TKTCPNGHC | LIVER | 562 | p.D567N | c.1699G>A | Missense_Mutation | 1 | 0.22 | C3A | N | 1 | 0 | 0 | N |
RET | TKTCPNGHC | LIVER | 562 | p.D567N | c.1699G>A | Missense_Mutation | 1 | 0.22 | HEPG2 | N | 1 | 0 | 0 | N |
RET | TYRLMLQCW | LARGE_INTESTINE | 980 | p.M980T | c.2939T>C | Missense_Mutation | 1 | 0.22 | HCT15 | Y | 1 | 9 | 0 | N |
RET | TYRLMLQCW | LARGE_INTESTINE | 980 | p.M980T | c.2939T>C | Missense_Mutation | 1 | 0.22 | HRT18 | Y | 1 | 9 | 0 | N |