A Database of Epigenetic Modifiers
Protein: SIRT1 |
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# | Cell Line/Tumor sample | Tissue of Origin | cDNA change | Protein change | Source | FATHMM Prediction | PolyPhen2 Prediction |
---|---|---|---|---|---|---|---|
1 | AU565 | BREAST | c.530C>T | p.T177I | CCLE | PASSENGER/OTHER | Probably Damaging |
2 | DV90 | LUNG | c.760_760delA | p.K254fs | CCLE | NP | NP |
3 | HEC108 | ENDOMETRIUM | c.2017A>G | p.S673G | CCLE | PASSENGER/OTHER | Probably Damaging |
4 | HEC251 | ENDOMETRIUM | c.1466T>C | p.L489S | CCLE | PASSENGER/OTHER | Probably Damaging |
5 | HEC59 | ENDOMETRIUM | c.1986A>T | p.E662D | CCLE | PASSENGER/OTHER | Benign |
6 | HPBALL | HAEMATOPOIETIC AND LYMPHOID TISSUE | c.1874C>T | p.P625L | CCLE | PASSENGER/OTHER | Possibly Damaging |
7 | IM95 | STOMACH | c.703_703delA | p.K235fs | CCLE | NP | NP |
8 | JHUEM7 | ENDOMETRIUM | c.1547G>A | p.R516Q | CCLE | PASSENGER/OTHER | Probably Damaging |
9 | KM12 | LARGE INTESTINE | c.1220T>C | p.M407T | CCLE | PASSENGER/OTHER | Probably Damaging |
10 | LN18 | CENTRAL NERVOUS SYSTEM | c.1178C>G | p.P393R | CCLE | PASSENGER/OTHER | Probably Damaging |
11 | NCIH146 | LUNG | c.1896G>T | p.Q632H | CCLE | PASSENGER/OTHER | Probably Damaging |
12 | NCIH1836 | LUNG | c.1484G>A | p.G495D | CCLE | PASSENGER/OTHER | Benign |
13 | PF382 | HAEMATOPOIETIC AND LYMPHOID TISSUE | c.1949A>G | p.Y650C | CCLE | PASSENGER/OTHER | Benign |
14 | REH | HAEMATOPOIETIC AND LYMPHOID TISSUE | c.1946G>A | p.R649H | CCLE | PASSENGER/OTHER | Probably Damaging |
15 | SCC4 | UPPER AERODIGESTIVE TRACT | c.809T>A | p.I270K | CCLE | PASSENGER/OTHER | Probably Damaging |
16 | SNGM | ENDOMETRIUM | c.596G>A | p.R199Q | CCLE | PASSENGER/OTHER | Probably Damaging |
17 | SNU1079 | BILIARY TRACT | c.441G>T | p.L147L | CCLE | NP | NP |
18 | SNU1197 | LARGE INTESTINE | c.2134G>A | p.A712T | CCLE | PASSENGER/OTHER | Benign |
19 | SNU81 | LARGE INTESTINE | c.2174A>G | p.E725G | CCLE | PASSENGER/OTHER | Benign |
20 | SNU81 | LARGE INTESTINE | c.713A>C | p.K238T | CCLE | PASSENGER/OTHER | Benign |
21 | SW620 | LARGE INTESTINE | c.1147G>A | p.V383I | CCLE | PASSENGER/OTHER | Benign |
22 | T84 | LARGE INTESTINE | c.1135G>A | p.D379N | CCLE | PASSENGER/OTHER | Possibly Damaging |
23 | TF1 | HAEMATOPOIETIC AND LYMPHOID TISSUE | c.1439G>A | p.G480E | CCLE | PASSENGER/OTHER | Probably Damaging |
24 | YD15 | SALIVARY GLAND | c.1294G>A | p.E432K | CCLE | PASSENGER/OTHER | Benign |
25 | ZR7530 | BREAST | c.2215G>T | p.D739Y | CCLE | PASSENGER/OTHER | Possibly Damaging |
26 | 587342 | LARGE INTESTINE | c.760delA | p.I256fs*2 | COSMIC | NP | NP |
27 | 631084 | LUNG | c.770T>G | p.I257R | COSMIC | PASSENGER/OTHER | Probably Damaging |
28 | ESO-185 | OESOPHAGUS | c.963C>T | p.F321F | COSMIC | NP | NP |
29 | HCC2998 | LARGE INTESTINE | c.1558G>T | p.E520* | COSMIC | NP | NP |
30 | HCC2998 | LARGE INTESTINE | c.2059G>A | p.E687K | COSMIC | PASSENGER/OTHER | Probably Damaging |
31 | KM12 | LARGE INTESTINE | c.1220T>C | p.M407T | COSMIC | PASSENGER/OTHER | Probably Damaging |
32 | LUAD-RT-S01477 | LUNG | c.1646C>G | p.S549C | COSMIC | PASSENGER/OTHER | Probably Damaging |
33 | MB_Exm599 | CENTRAL NERVOUS SYSTEM | c.1945C>T | p.R649C | COSMIC | PASSENGER/OTHER | Probably Damaging |
34 | TCGA-30-1857-01 | OVARY | c.477C>T | p.S159S | COSMIC | NP | NP |
35 | TCGA-55-6968-01 | LUNG | c.1646C>T | p.S549F | COSMIC | PASSENGER/OTHER | Probably Damaging |
36 | TCGA-67-3771-01 | LUNG | c.892G>C | p.D298H | COSMIC | PASSENGER/OTHER | Probably Damaging |
37 | TCGA-85-6561-01 | LUNG | c.844C>A | p.R282S | COSMIC | PASSENGER/OTHER | Probably Damaging |
38 | TCGA-A6-6141-01 | LARGE INTESTINE | c.1021C>T | p.R341C | COSMIC | PASSENGER/OTHER | Probably Damaging |
39 | TCGA-AA-3672-01 | LARGE INTESTINE | c.1850C>T | p.A617V | COSMIC | PASSENGER/OTHER | Benign |
40 | TCGA-AA-3811-01 | LARGE INTESTINE | c.1105G>A | p.A369T | COSMIC | PASSENGER/OTHER | Probably Damaging |
41 | TCGA-AA-A00J-01 | LARGE INTESTINE | c.1282T>C | p.Y428H | COSMIC | PASSENGER/OTHER | Benign |
42 | TCGA-AA-A00N-01 | LARGE INTESTINE | c.1547G>A | p.R516Q | COSMIC | PASSENGER/OTHER | Probably Damaging |
43 | TCGA-AG-A002-01 | LARGE INTESTINE | c.444C>T | p.F148F | COSMIC | NP | NP |
44 | TCGA-AG-A002-01 | LARGE INTESTINE | c.943G>T | p.E315* | COSMIC | NP | NP |
45 | TCGA-AP-A0LM-01 | ENDOMETRIUM | c.1208C>T | p.P403L | COSMIC | PASSENGER/OTHER | Benign |
46 | TCGA-AP-A0LM-01 | ENDOMETRIUM | c.2188G>T | p.A730S | COSMIC | PASSENGER/OTHER | Benign |
47 | TCGA-AP-A0LM-01 | ENDOMETRIUM | c.845G>A | p.R282H | COSMIC | PASSENGER/OTHER | Probably Damaging |
48 | TCGA-AX-A05Z-01 | ENDOMETRIUM | c.1558G>T | p.E520* | COSMIC | NP | NP |
49 | TCGA-AZ-4315-01 | LARGE INTESTINE | c.2024G>A | p.S675N | COSMIC | PASSENGER/OTHER | Probably Damaging |
50 | TCGA-B0-5703-01 | KIDNEY | c.876T>A | p.D292E | COSMIC | PASSENGER/OTHER | Probably Damaging |
51 | TCGA-B0-5703-01 | KIDNEY | c.877C>T | p.P293S | COSMIC | PASSENGER/OTHER | Probably Damaging |
52 | TCGA-B5-A0JY-01 | ENDOMETRIUM | c.1399G>T | p.E467* | COSMIC | NP | NP |
53 | TCGA-B5-A11E-01 | ENDOMETRIUM | c.1945C>T | p.R649C | COSMIC | PASSENGER/OTHER | Probably Damaging |
54 | TCGA-B5-A11M-01 | ENDOMETRIUM | c.1423G>T | p.D475Y | COSMIC | PASSENGER/OTHER | Probably Damaging |
55 | TCGA-BH-A18U-01 | BREAST | c.1852G>A | p.G618R | COSMIC | PASSENGER/OTHER | Benign |
56 | TCGA-BS-A0UJ-01 | ENDOMETRIUM | c.1260A>G | p.E420E | COSMIC | NP | NP |
57 | TCGA-CK-6746-01 | LARGE INTESTINE | c.1236_1237insT | p.G415fs*2 | COSMIC | NP | NP |
58 | TCGA-D1-A15X-01 | ENDOMETRIUM | c.2094C>T | p.F698F | COSMIC | NP | NP |
59 | TCGA-E2-A1LG-01 | BREAST | c.2043G>C | p.Q681H | COSMIC | PASSENGER/OTHER | Benign |
60 | cSCCP7 | SKIN | c.1891G>A | p.E631K | COSMIC | PASSENGER/OTHER | Benign |
61 | pfg019T | STOMACH | c.1828delA | p.N611fs*10 | COSMIC | NP | NP |
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S. No. | Position | Amino acid | Type |
Proteomics DB | COSMIC | Gene Atlas | STRING | PIR |
SIRT1 | SIRT1 | SIRT1 | ENSP00000212015 | Q96EB6 |
QuickGO | HGNC | Ensembl Genome Browser | TreeFam | UniProt |
Q96EB6 | SIRT1 | ENSP00000212015 | SIRT1 | Q96EB6 |
Expression Atlas | Protein Atlas | OMIM | IntAct | PharmGKB |
SIRT1 | ENSP00000212015 | 604479 | Q96EB6 | PA37935 |