Primary Site >> Liver Cancer
Gene >> CNTN2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000331830 |
| Start | 205069517:205069517(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2152A>G |
| AA Mutation | p.Ser718Gly(p.S718G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000331830 |
| Start | 205071957:205071957(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2555G>T |
| AA Mutation | p.Trp852Leu(p.W852L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000331830 |
| Start | 205070450:205070450(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2456T>C |
| AA Mutation | p.Val819Ala(p.V819A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000331830 |
| Start | 205073719:205073719(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3077C>T |
| AA Mutation | p.Ser1026Phe(p.S1026F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000331830 |
| Start | 205067195:205067195(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2070T>G |
| AA Mutation | p.Ile690Met(p.I690M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000331830 |
| Start | 205057978:205057978(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.128C>T |
| AA Mutation | p.Pro43Leu(p.P43L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000331830 |
| Start | 205072502:205072502(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2751C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000331830 |
| Start | 205058045:205058045(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs750251767 |
| CDS Mutation | c.195C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000331830 |
| Start | 205058009:205058009(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.160delG |
| AA Mutation | p.Glu54ArgfsTer22(p.E54Rfs*22) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |