Primary Site >> Liver Cancer
Gene >> ABCC4
| ID | 1 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000376887 |
| Start | 95164379:95164379(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2174A>T |
| AA Mutation | p.Gln725Leu(p.Q725L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000376887 |
| Start | 95206699:95206699(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs377022090 |
| CDS Mutation | c.994G>A |
| AA Mutation | p.Val332Met(p.V332M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000376887 |
| Start | 95206656:95206656(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1037T>A |
| AA Mutation | p.Ile346Asn(p.I346N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000376887 |
| Start | 95234759:95234759(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.382T>G |
| AA Mutation | p.Ser128Ala(p.S128A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000376887 |
| Start | 95170571:95170571(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1785G>C |
| AA Mutation | p.Gln595His(p.Q595H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000376887 |
| Start | 95115946:95115946(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs148807118 |
| CDS Mutation | c.2511G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |