Primary Site >> Liver Cancer
Gene >> CNTN1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000347616 |
| Start | 41029169:41029169(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2930G>A |
| AA Mutation | p.Arg977His(p.R977H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000347616 |
| Start | 40993238:40993238(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2082A>G |
| AA Mutation | p.Ile694Met(p.I694M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000347616 |
| Start | 40918663:40918663(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.119G>T |
| AA Mutation | p.Gly40Val(p.G40V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000347616 |
| Start | 40937658:40937658(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1199T>C |
| AA Mutation | p.Ile400Thr(p.I400T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000347616 |
| Start | 41027871:41027871(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2725C>G |
| AA Mutation | p.Pro909Ala(p.P909A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000347616 |
| Start | 41016781:41016781(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs566695601 |
| CDS Mutation | c.2284C>T |
| AA Mutation | p.Pro762Ser(p.P762S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000347616 |
| Start | 40980982:40980982(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1878T>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000347616 |
| Start | 40924636:40924636(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs771697105 |
| CDS Mutation | c.480C>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |