Primary Site >> Liver Cancer
Gene >> PAM
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000438793 |
| Start | 102990362:102990362(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1574T>C |
| AA Mutation | p.Leu525Pro(p.L525P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000438793 |
| Start | 103025287:103025287(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2642T>A |
| AA Mutation | p.Leu881Gln(p.L881Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000438793 |
| Start | 102901357:102901357(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.212C>A |
| AA Mutation | p.Ser71Tyr(p.S71Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000438793 |
| Start | 102867307:102867307(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.124T>A |
| AA Mutation | p.Cys42Ser(p.C42S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000438793 |
| Start | 102990342:102990342(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs756785296 |
| CDS Mutation | c.1554T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000438793 |
| Start | 103025237:103025237(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2592G>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000438793 |
| Start | 103007494:103007494(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2052T>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |