Primary Site >> Stomach Cancer
Gene >> VIM
| ID | 1 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000224237 |
| Start | 17234694:17234694(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs747735685 |
| CDS Mutation | c.884T>C |
| AA Mutation | p.Phe295Ser(p.F295S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000224237 |
| Start | 17235878:17235878(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1262T>C |
| AA Mutation | p.Leu421Pro(p.L421P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000224237 |
| Start | 17236321:17236321(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1301T>C |
| AA Mutation | p.Val434Ala(p.V434A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000224237 |
| Start | 17235207:17235207(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1047G>T |
| AA Mutation | p.Glu349Asp(p.E349D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000224237 |
| Start | 17235329:17235329(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1169A>C |
| AA Mutation | p.Lys390Thr(p.K390T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000224237 |
| Start | 17233858:17233858(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.809G>A |
| AA Mutation | p.Arg270His(p.R270H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000224237 |
| Start | 17234766:17234766(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.956A>G |
| AA Mutation | p.Tyr319Cys(p.Y319C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000224237 |
| Start | 17233846:17233846(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs150878383 |
| CDS Mutation | c.797C>T |
| AA Mutation | p.Thr266Met(p.T266M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000224237 |
| Start | 17235381:17235381(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1221G>T |
| AA Mutation | p.Glu407Asp(p.E407D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000224237 |
| Start | 17234731:17234731(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs770500248 |
| CDS Mutation | c.921C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |