Primary Site >> Stomach Cancer
Gene >> ENPEP
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265162 |
| Start | 110476703:110476703(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs534876489 |
| CDS Mutation | c.289G>A |
| AA Mutation | p.Val97Ile(p.V97I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265162 |
| Start | 110553449:110553449(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2636T>C |
| AA Mutation | p.Val879Ala(p.V879A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265162 |
| Start | 110561545:110561545(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2861T>G |
| AA Mutation | p.Leu954Arg(p.L954R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265162 |
| Start | 110543034:110543034(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs142728357 |
| CDS Mutation | c.1964G>A |
| AA Mutation | p.Arg655His(p.R655H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265162 |
| Start | 110476914:110476914(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.500A>C |
| AA Mutation | p.Glu167Ala(p.E167A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265162 |
| Start | 110476979:110476979(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.565A>G |
| AA Mutation | p.Thr189Ala(p.T189A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265162 |
| Start | 110488546:110488546(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs773121479 |
| CDS Mutation | c.650T>C |
| AA Mutation | p.Ile217Thr(p.I217T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265162 |
| Start | 110476461:110476461(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.47C>T |
| AA Mutation | p.Thr16Met(p.T16M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265162 |
| Start | 110476485:110476485(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs770659499 |
| CDS Mutation | c.71C>T |
| AA Mutation | p.Ala24Val(p.A24V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265162 |
| Start | 110513440:110513440(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1334T>C |
| AA Mutation | p.Val445Ala(p.V445A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265162 |
| Start | 110549359:110549359(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2165G>A |
| AA Mutation | p.Gly722Asp(p.G722D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000265162 |
| Start | 110476729:110476729(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.315C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000265162 |
| Start | 110553354:110553354(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2541T>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000265162 |
| Start | 110476792:110476792(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.378C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000265162 |
| Start | 110476651:110476651(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.237G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000265162 |
| Start | 110477041:110477041(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.627G>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000265162 |
| Start | 110520355:110520355(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1716T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000265162 |
| Start | 110513441:110513441(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1335A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000265162 |
| Start | 110476688:110476688(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.274C>T |
| AA Mutation | p.Arg92Ter(p.R92*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000265162 |
| Start | 110520051:110520052(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.1558dupT |
| AA Mutation | p.Trp520LeufsTer9(p.W520Lfs*9) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000265162 |
| Start | 110491085:110491086(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.843dupC |
| AA Mutation | p.Met282HisfsTer14(p.M282Hfs*14) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000265162 |
| Start | 110561414:110561415(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | rs768719919 |
| CDS Mutation | c.2736dupT |
| AA Mutation | p.Ala913CysfsTer13(p.A913Cfs*13) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |