Primary Site >> Stomach Cancer
Gene >> TRA2B
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000453386 |
| Start | 185923849:185923849(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.469C>T |
| AA Mutation | p.Arg157Cys(p.R157C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000453386 |
| Start | 185925603:185925603(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs777354455 |
| CDS Mutation | c.194G>A |
| AA Mutation | p.Arg65Gln(p.R65Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000453386 |
| Start | 185918409:185918409(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs564623776 |
| CDS Mutation | c.812G>A |
| AA Mutation | p.Arg271His(p.R271H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000453386 |
| Start | 185925481:185925481(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.316C>T |
| AA Mutation | p.Arg106Cys(p.R106C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000453386 |
| Start | 185925577:185925577(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs766786702 |
| CDS Mutation | c.220C>T |
| AA Mutation | p.Arg74Cys(p.R74C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000453386 |
| Start | 185923836:185923836(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.482T>C |
| AA Mutation | p.Phe161Ser(p.F161S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000453386 |
| Start | 185922046:185922046(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs375780205 |
| CDS Mutation | c.603G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |