Primary Site >> Liver Cancer
Gene >> MECOM
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000494292 |
| Start | 169381419:169381419(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.143C>A |
| AA Mutation | p.Ser48Tyr(p.S48Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000468789 |
| Start | 169122656:169122656(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.338A>T |
| AA Mutation | p.Asn113Ile(p.N113I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000468789 |
| Start | 169115606:169115606(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1702C>G |
| AA Mutation | p.Pro568Ala(p.P568A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000468789 |
| Start | 169089139:169089139(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs779967808 |
| CDS Mutation | c.2882A>G |
| AA Mutation | p.His961Arg(p.H961R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000468789 |
| Start | 169122615:169122615(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.379A>T |
| AA Mutation | p.Ser127Cys(p.S127C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000468789 |
| Start | 169121108:169121108(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs185054275 |
| CDS Mutation | c.516G>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |