Primary Site >> Stomach Cancer
Gene >> PCYT1B
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379144 |
| Start | 24575233:24575233(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.794A>G |
| AA Mutation | p.Asn265Ser(p.N265S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379144 |
| Start | 24579353:24579353(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.671G>A |
| AA Mutation | p.Gly224Glu(p.G224E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379144 |
| Start | 24590112:24590112(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.397T>A |
| AA Mutation | p.Tyr133Asn(p.Y133N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379144 |
| Start | 24590034:24590034(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.475G>A |
| AA Mutation | p.Glu159Lys(p.E159K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379145 |
| Start | 24672575:24672575(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs191876455 |
| CDS Mutation | c.58C>T |
| AA Mutation | p.Arg20Cys(p.R20C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000379144 |
| Start | 24590134:24590134(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs757374830 |
| CDS Mutation | c.375C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |