Primary Site >> Liver Cancer
Gene >> ASAP1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000518721 |
| Start | 130092025:130092025(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2520C>A |
| AA Mutation | p.Asp840Glu(p.D840E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000518721 |
| Start | 130159914:130159914(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.960T>A |
| AA Mutation | p.Asn320Lys(p.N320K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000518721 |
| Start | 130118563:130118563(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1720A>T |
| AA Mutation | p.Arg574Trp(p.R574W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000518721 |
| Start | 130169011:130169011(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.803T>G |
| AA Mutation | p.Leu268Arg(p.L268R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000518721 |
| Start | 130134330:130134330(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1183C>T |
| AA Mutation | p.His395Tyr(p.H395Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000518721 |
| Start | 130118642:130118642(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs749003615 |
| CDS Mutation | c.1641T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |