Primary Site >> Stomach Cancer
Gene >> B3GNT8
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000321702 |
| Start | 41425692:41425692(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1087A>G |
| AA Mutation | p.Thr363Ala(p.T363A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000321702 |
| Start | 41425769:41425769(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1010C>T |
| AA Mutation | p.Thr337Ile(p.T337I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000321702 |
| Start | 41426181:41426181(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.598G>A |
| AA Mutation | p.Ala200Thr(p.A200T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000321702 |
| Start | 41426612:41426612(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.167C>A |
| AA Mutation | p.Ala56Asp(p.A56D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000321702 |
| Start | 41426470:41426470(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs764666731 |
| CDS Mutation | c.309C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000321702 |
| Start | 41426501:41426501(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.278delG |
| AA Mutation | p.Gly93AlafsTer75(p.G93Afs*75) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |