Primary Site >> Stomach Cancer
Gene >> EP400
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389562 |
| Start | 132029802:132029802(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5483G>A |
| AA Mutation | p.Gly1828Asp(p.G1828D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389562 |
| Start | 131960954:131960954(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs764793090 |
| CDS Mutation | c.335G>A |
| AA Mutation | p.Arg112Gln(p.R112Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389562 |
| Start | 132069501:132069501(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs189173886 |
| CDS Mutation | c.8881G>A |
| AA Mutation | p.Ala2961Thr(p.A2961T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389562 |
| Start | 131986536:131986536(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1952C>A |
| AA Mutation | p.Pro651His(p.P651H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389562 |
| Start | 132006844:132006844(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3271A>T |
| AA Mutation | p.Ile1091Phe(p.I1091F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000389562 |
| Start | 132062111:132062111(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.7886C>T |
| AA Mutation | p.Thr2629Met(p.T2629M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389562 |
| Start | 132062619:132062619(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs531098130 |
| CDS Mutation | c.8252C>T |
| AA Mutation | p.Thr2751Met(p.T2751M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389562 |
| Start | 132064789:132064789(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.8456C>A |
| AA Mutation | p.Pro2819Gln(p.P2819Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389562 |
| Start | 132066966:132066966(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.8746G>A |
| AA Mutation | p.Ala2916Thr(p.A2916T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389562 |
| Start | 131979770:131979770(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs111485547 |
| CDS Mutation | c.1412C>T |
| AA Mutation | p.Ala471Val(p.A471V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389562 |
| Start | 131982179:131982179(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs190189185 |
| CDS Mutation | c.1630G>A |
| AA Mutation | p.Val544Met(p.V544M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389562 |
| Start | 131979733:131979733(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1375A>C |
| AA Mutation | p.Ser459Arg(p.S459R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389562 |
| Start | 132021120:132021120(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4489G>A |
| AA Mutation | p.Ala1497Thr(p.A1497T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389562 |
| Start | 132023851:132023851(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4765C>T |
| AA Mutation | p.Pro1589Ser(p.P1589S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389562 |
| Start | 132050383:132050383(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.7261C>T |
| AA Mutation | p.His2421Tyr(p.H2421Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389562 |
| Start | 132020126:132020126(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs553207849 |
| CDS Mutation | c.4355C>T |
| AA Mutation | p.Thr1452Met(p.T1452M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389562 |
| Start | 132044204:132044204(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.6478T>C |
| AA Mutation | p.Trp2160Arg(p.W2160R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389562 |
| Start | 132053210:132053210(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs752491607 |
| CDS Mutation | c.7459G>A |
| AA Mutation | p.Ala2487Thr(p.A2487T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389562 |
| Start | 132028044:132028044(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs754032425 |
| CDS Mutation | c.5137C>T |
| AA Mutation | p.Arg1713Cys(p.R1713C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389562 |
| Start | 132013127:132013127(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs773523648 |
| CDS Mutation | c.3560G>A |
| AA Mutation | p.Arg1187His(p.R1187H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389562 |
| Start | 132020171:132020171(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4400G>A |
| AA Mutation | p.Arg1467Gln(p.R1467Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389562 |
| Start | 132020192:132020192(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201077052 |
| CDS Mutation | c.4421C>T |
| AA Mutation | p.Thr1474Met(p.T1474M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389562 |
| Start | 132077663:132077663(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs779770506 |
| CDS Mutation | c.9362C>T |
| AA Mutation | p.Pro3121Leu(p.P3121L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389562 |
| Start | 131979746:131979746(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs779183271 |
| CDS Mutation | c.1388C>T |
| AA Mutation | p.Thr463Met(p.T463M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389562 |
| Start | 132055134:132055134(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.7810G>A |
| AA Mutation | p.Ala2604Thr(p.A2604T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389562 |
| Start | 131990685:131990685(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2600C>T |
| AA Mutation | p.Ala867Val(p.A867V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 27 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389562 |
| Start | 132045411:132045411(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.6877C>T |
| AA Mutation | p.Arg2293Cys(p.R2293C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 28 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389562 |
| Start | 132062165:132062165(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.7940C>T |
| AA Mutation | p.Ala2647Val(p.A2647V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 29 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389562 |
| Start | 131961121:131961121(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.502G>T |
| AA Mutation | p.Gly168Trp(p.G168W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 30 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389562 |
| Start | 131990066:131990066(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2512G>A |
| AA Mutation | p.Ala838Thr(p.A838T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 31 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389562 |
| Start | 132030039:132030039(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5635C>T |
| AA Mutation | p.Arg1879Cys(p.R1879C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 32 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389562 |
| Start | 131987841:131987841(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2360C>A |
| AA Mutation | p.Ala787Asp(p.A787D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 33 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389562 |
| Start | 132028134:132028134(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5227A>G |
| AA Mutation | p.Ser1743Gly(p.S1743G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 34 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389562 |
| Start | 132045856:132045856(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.7156C>T |
| AA Mutation | p.Arg2386Trp(p.R2386W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 35 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389562 |
| Start | 132029721:132029721(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs545633950 |
| CDS Mutation | c.5402C>T |
| AA Mutation | p.Pro1801Leu(p.P1801L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 36 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389562 |
| Start | 132030048:132030048(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5644C>A |
| AA Mutation | p.Leu1882Met(p.L1882M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 37 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389562 |
| Start | 132006238:132006238(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs769700878 |
| CDS Mutation | c.3062T>C |
| AA Mutation | p.Ile1021Thr(p.I1021T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 38 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000389562 |
| Start | 132023832:132023832(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs756591889 |
| CDS Mutation | c.4746C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 39 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000389562 |
| Start | 132027441:132027441(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs762022153 |
| CDS Mutation | c.5019C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 40 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000389562 |
| Start | 132044272:132044272(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs537614857 |
| CDS Mutation | c.6546G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 41 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000389562 |
| Start | 132055196:132055196(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.7872T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 42 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000389562 |
| Start | 132020082:132020082(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs113843264 |
| CDS Mutation | c.4311C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 43 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000389562 |
| Start | 132025740:132025740(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4950G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 44 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000389562 |
| Start | 131960853:131960853(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs141965996 |
| CDS Mutation | c.234C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 45 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000389562 |
| Start | 132064742:132064742(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs368496363 |
| CDS Mutation | c.8409G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 46 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000389562 |
| Start | 131961888:131961888(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs753728916 |
| CDS Mutation | c.1269G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 47 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000389562 |
| Start | 132023853:132023853(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4767G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 48 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000389562 |
| Start | 132067369:132067369(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.8757C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 49 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000389562 |
| Start | 132006170:132006170(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs746911998 |
| CDS Mutation | c.2994G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 50 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000389562 |
| Start | 132021083:132021083(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4452A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 51 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000389562 |
| Start | 132062271:132062271(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.8046C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 52 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000389562 |
| Start | 132017538:132017538(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3927T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 53 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000389562 |
| Start | 132044829:132044829(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs147763834 |
| CDS Mutation | c.6660C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |