Primary Site >> Stomach Cancer
Gene >> AVP
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000380293 |
| Start | 3084562:3084562(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.113T>C |
| AA Mutation | p.Leu38Pro(p.L38P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000380293 |
| Start | 3084653:3084653(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs747008249 |
| CDS Mutation | c.22G>A |
| AA Mutation | p.Ala8Thr(p.A8T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000380293 |
| Start | 3084601:3084601(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.74G>A |
| AA Mutation | p.Cys25Tyr(p.C25Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000380293 |
| Start | 3084575:3084575(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.100T>G |
| AA Mutation | p.Ser34Ala(p.S34A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000380293 |
| Start | 3084591:3084591(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs764339248 |
| CDS Mutation | c.84C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000380293 |
| Start | 3084592:3084592(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.83delG |
| AA Mutation | p.Gly28AlafsTer11(p.G28Afs*11) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |