Primary Site >> Liver Cancer
Gene >> ERC1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360905 |
| Start | 1083394:1083394(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.900G>C |
| AA Mutation | p.Gln300His(p.Q300H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360905 |
| Start | 1083282:1083282(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.788C>G |
| AA Mutation | p.Thr263Arg(p.T263R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360905 |
| Start | 1444731:1444731(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3194A>T |
| AA Mutation | p.Gln1065Leu(p.Q1065L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360905 |
| Start | 1083554:1083554(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1060G>A |
| AA Mutation | p.Glu354Lys(p.E354K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360905 |
| Start | 1408236:1408236(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3013T>A |
| AA Mutation | p.Ser1005Thr(p.S1005T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000360905 |
| Start | 1028098:1028098(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs745971025 |
| CDS Mutation | c.195C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |