Primary Site >> Liver Cancer
Gene >> INPP4B
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262992 |
| Start | 142305470:142305470(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs753433691 |
| CDS Mutation | c.491T>C |
| AA Mutation | p.Val164Ala(p.V164A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262992 |
| Start | 142028839:142028839(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2718G>T |
| AA Mutation | p.Met906Ile(p.M906I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262992 |
| Start | 142145908:142145908(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1652G>C |
| AA Mutation | p.Gly551Ala(p.G551A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000262992 |
| Start | 142086213:142086213(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs769799344 |
| CDS Mutation | c.2418A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000262992 |
| Start | 142405311:142405311(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.150C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | splice_acceptor_variant |
| Transcription ID | ENST00000262992 |
| Start | 142403056:142403056(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.256-2A>T |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |