Primary Site >> Stomach Cancer
Gene >> UGT8
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000310836 |
| Start | 114623472:114623472(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.592G>A |
| AA Mutation | p.Gly198Ser(p.G198S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000310836 |
| Start | 114675984:114675984(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1322T>A |
| AA Mutation | p.Val441Asp(p.V441D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000310836 |
| Start | 114676040:114676040(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1378C>A |
| AA Mutation | p.Leu460Ile(p.L460I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000310836 |
| Start | 114623067:114623067(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs114818124 |
| CDS Mutation | c.187G>A |
| AA Mutation | p.Ala63Thr(p.A63T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000310836 |
| Start | 114623440:114623440(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.560G>A |
| AA Mutation | p.Arg187His(p.R187H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000310836 |
| Start | 114676021:114676021(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1359T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000310836 |
| Start | 114623018:114623018(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs768880144 |
| CDS Mutation | c.138C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000310836 |
| Start | 114676078:114676078(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1421delT |
| AA Mutation | p.Leu474TyrfsTer22(p.L474Yfs*22) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000310836 |
| Start | 114665733:114665733(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1019G>A |
| AA Mutation | p.Trp340Ter(p.W340*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |