Primary Site >> Liver Cancer
Gene >> SCN5A
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333535 |
| Start | 38581308:38581308(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2851G>A |
| AA Mutation | p.Asp951Asn(p.D951N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333535 |
| Start | 38603851:38603851(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1751G>A |
| AA Mutation | p.Gly584Asp(p.G584D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333535 |
| Start | 38599029:38599029(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1912G>A |
| AA Mutation | p.Gly638Ser(p.G638S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333535 |
| Start | 38609921:38609921(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.747G>C |
| AA Mutation | p.Lys249Asn(p.K249N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333535 |
| Start | 38555753:38555753(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4445G>T |
| AA Mutation | p.Gly1482Val(p.G1482V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000333535 |
| Start | 38575317:38575317(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3646C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000333535 |
| Start | 38604051:38604051(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1551G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000333535 |
| Start | 38609795:38609795(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs376515775 |
| CDS Mutation | c.873C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000333535 |
| Start | 38603838:38603838(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs775985491 |
| CDS Mutation | c.1764T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |