Primary Site >> Liver Cancer
Gene >> IDH1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000345146 |
| Start | 208239964:208239964(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.890G>C |
| AA Mutation | p.Cys297Ser(p.C297S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000345146 |
| Start | 208248389:208248389(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.394C>G |
| AA Mutation | p.Arg132Gly(p.R132G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000345146 |
| Start | 208248389:208248389(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs121913499 |
| CDS Mutation | c.394C>T |
| AA Mutation | p.Arg132Cys(p.R132C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000345146 |
| Start | 208243581:208243581(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.544A>G |
| AA Mutation | p.Met182Val(p.M182V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000345146 |
| Start | 208245327:208245327(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.512A>C |
| AA Mutation | p.Asn171Thr(p.N171T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000345146 |
| Start | 208243532:208243532(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.593A>C |
| AA Mutation | p.Gln198Pro(p.Q198P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |