Primary Site >> Stomach Cancer
Gene >> VPS9D1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389386 |
| Start | 89710612:89710612(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs776117646 |
| CDS Mutation | c.1232C>T |
| AA Mutation | p.Ala411Val(p.A411V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389386 |
| Start | 89710613:89710613(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs761322702 |
| CDS Mutation | c.1231G>A |
| AA Mutation | p.Ala411Thr(p.A411T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389386 |
| Start | 89711376:89711376(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.784A>G |
| AA Mutation | p.Asn262Asp(p.N262D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389386 |
| Start | 89712651:89712651(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.497G>A |
| AA Mutation | p.Arg166Gln(p.R166Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389386 |
| Start | 89709874:89709874(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1291G>A |
| AA Mutation | p.Glu431Lys(p.E431K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389386 |
| Start | 89709844:89709844(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs747712289 |
| CDS Mutation | c.1321C>T |
| AA Mutation | p.Arg441Cys(p.R441C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389386 |
| Start | 89716616:89716616(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.277C>T |
| AA Mutation | p.Arg93Cys(p.R93C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389386 |
| Start | 89710589:89710589(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs769766323 |
| CDS Mutation | c.1255G>A |
| AA Mutation | p.Val419Ile(p.V419I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389386 |
| Start | 89709292:89709292(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201610914 |
| CDS Mutation | c.1532C>T |
| AA Mutation | p.Ala511Val(p.A511V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389386 |
| Start | 89708481:89708481(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1748G>A |
| AA Mutation | p.Gly583Asp(p.G583D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000389386 |
| Start | 89707864:89707864(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1893G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000389386 |
| Start | 89716743:89716743(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs778936154 |
| CDS Mutation | c.255G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000389386 |
| Start | 89709821:89709821(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs754254812 |
| CDS Mutation | c.1344A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000389386 |
| Start | 89716800:89716800(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.198delC |
| AA Mutation | p.Asp67ThrfsTer6(p.D67Tfs*6) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |