Primary Site >> Liver Cancer
Gene >> FANCD2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000383807 |
| Start | 10060379:10060379(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1742T>C |
| AA Mutation | p.Met581Thr(p.M581T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000383807 |
| Start | 10032919:10032919(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.152T>G |
| AA Mutation | p.Leu51Arg(p.L51R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000383807 |
| Start | 10095264:10095264(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4028G>A |
| AA Mutation | p.Gly1343Glu(p.G1343E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000383807 |
| Start | 10043128:10043128(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs370641659 |
| CDS Mutation | c.967T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000383807 |
| Start | 10041705:10041705(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs756621826 |
| CDS Mutation | c.778T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000383807 |
| Start | 10087149:10087149(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs566518051 |
| CDS Mutation | c.3351C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |