Primary Site >> Stomach Cancer
Gene >> UGT1A6
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000305139 |
| Start | 233693854:233693854(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.850G>T |
| AA Mutation | p.Asp284Tyr(p.D284Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000305139 |
| Start | 233772515:233772515(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs553499095 |
| CDS Mutation | c.1555A>G |
| AA Mutation | p.Lys519Glu(p.K519E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000305139 |
| Start | 233693835:233693835(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs764583792 |
| CDS Mutation | c.831C>G |
| AA Mutation | p.Ile277Met(p.I277M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000305139 |
| Start | 233772500:233772500(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1540C>T |
| AA Mutation | p.Arg514Trp(p.R514W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000305139 |
| Start | 233772427:233772427(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs114123636 |
| CDS Mutation | c.1467C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000305139 |
| Start | 233693478:233693478(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.474C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000305139 |
| Start | 233772515:233772515(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.1560delA |
| AA Mutation | p.Arg522GlufsTer22(p.R522Efs*22) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000305139 |
| Start | 233693616:233693616(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs779391112 |
| CDS Mutation | c.616delT |
| AA Mutation | p.Ser206ProfsTer38(p.S206Pfs*38) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000305139 |
| Start | 233693308:233693308(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.304C>T |
| AA Mutation | p.Arg102Ter(p.R102*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |