Primary Site >> Stomach Cancer
Gene >> APOBEC3B
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333467 |
| Start | 38992136:38992136(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs747995529 |
| CDS Mutation | c.1121G>A |
| AA Mutation | p.Arg374Gln(p.R374Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333467 |
| Start | 38992067:38992067(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs1053813 |
| CDS Mutation | c.1052G>A |
| AA Mutation | p.Arg351His(p.R351H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333467 |
| Start | 38986067:38986067(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.430C>A |
| AA Mutation | p.Arg144Ser(p.R144S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333467 |
| Start | 38986378:38986378(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.535G>A |
| AA Mutation | p.Ala179Thr(p.A179T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333467 |
| Start | 38991620:38991620(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1012T>C |
| AA Mutation | p.Tyr338His(p.Y338H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333467 |
| Start | 38984098:38984098(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs551433639 |
| CDS Mutation | c.41G>A |
| AA Mutation | p.Arg14Gln(p.R14Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |