Primary Site >> Liver Cancer
Gene >> CNTN6
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000350110 |
| Start | 1325947:1325947(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1079C>A |
| AA Mutation | p.Pro360Gln(p.P360Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000350110 |
| Start | 1329814:1329814(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs142802849 |
| CDS Mutation | c.1243G>A |
| AA Mutation | p.Val415Ile(p.V415I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000350110 |
| Start | 1383400:1383400(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2509G>T |
| AA Mutation | p.Gly837Cys(p.G837C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000350110 |
| Start | 1329847:1329847(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1276G>A |
| AA Mutation | p.Asp426Asn(p.D426N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000350110 |
| Start | 1329848:1329848(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1277A>T |
| AA Mutation | p.Asp426Val(p.D426V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000350110 |
| Start | 1402395:1402395(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs773206932 |
| CDS Mutation | c.2895A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |