Primary Site >> Liver Cancer
Gene >> ADGRB1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000323289 |
| Start | 142521975:142521975(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs761237409 |
| CDS Mutation | c.3035C>T |
| AA Mutation | p.Thr1012Met(p.T1012M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000323289 |
| Start | 142477272:142477272(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1216T>G |
| AA Mutation | p.Cys406Gly(p.C406G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000323289 |
| Start | 142542061:142542061(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3827T>C |
| AA Mutation | p.Phe1276Ser(p.F1276S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000323289 |
| Start | 142542353:142542353(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4119G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000323289 |
| Start | 142541987:142541987(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3753C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000323289 |
| Start | 142481705:142481705(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs376677183 |
| CDS Mutation | c.2124C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000323289 |
| Start | 142518188:142518188(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs770399870 |
| CDS Mutation | c.2868C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000323289 |
| Start | 142481555:142481555(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1974T>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000323289 |
| Start | 142464726:142464726(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.531delG |
| AA Mutation | p.Asn178ThrfsTer59(p.N178Tfs*59) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000323289 |
| Start | 142477136:142477136(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1080G>A |
| AA Mutation | p.Trp360Ter(p.W360*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | splice_acceptor_variant |
| Transcription ID | ENST00000323289 |
| Start | 142543599:142543599(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4450-2A>G |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |