Primary Site >> Stomach Cancer
Gene >> ACVR2B
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000352511 |
| Start | 38483289:38483289(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1496C>T |
| AA Mutation | p.Ser499Phe(p.S499F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000352511 |
| Start | 38482271:38482271(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1148G>A |
| AA Mutation | p.Arg383His(p.R383H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000352511 |
| Start | 38482559:38482559(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs761653104 |
| CDS Mutation | c.1343C>T |
| AA Mutation | p.Pro448Leu(p.P448L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000352511 |
| Start | 38483253:38483253(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1460G>A |
| AA Mutation | p.Gly487Asp(p.G487D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000352511 |
| Start | 38478159:38478159(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs539715843 |
| CDS Mutation | c.389C>T |
| AA Mutation | p.Pro130Leu(p.P130L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000352511 |
| Start | 38477366:38477366(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs756779787 |
| CDS Mutation | c.132C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000352511 |
| Start | 38478443:38478443(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.591T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000352511 |
| Start | 38483206:38483206(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs373661579 |
| CDS Mutation | c.1413G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000352511 |
| Start | 38477381:38477381(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201686292 |
| CDS Mutation | c.147C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000352511 |
| Start | 38482308:38482308(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1185G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000352511 |
| Start | 38483203:38483203(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs141985115 |
| CDS Mutation | c.1410C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000352511 |
| Start | 38478165:38478165(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.399delC |
| AA Mutation | p.Thr134ProfsTer54(p.T134Pfs*54) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |