Primary Site >> Liver Cancer
Gene >> VCAN
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265077 |
| Start | 83520272:83520272(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1966T>C |
| AA Mutation | p.Phe656Leu(p.F656L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265077 |
| Start | 83520623:83520623(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2317A>T |
| AA Mutation | p.Thr773Ser(p.T773S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265077 |
| Start | 83539628:83539628(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.6625A>C |
| AA Mutation | p.Thr2209Pro(p.T2209P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265077 |
| Start | 83541198:83541198(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.8195C>A |
| AA Mutation | p.Ala2732Glu(p.A2732E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265077 |
| Start | 83520968:83520968(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2662T>A |
| AA Mutation | p.Ser888Thr(p.S888T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265077 |
| Start | 83540820:83540820(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.7817A>G |
| AA Mutation | p.His2606Arg(p.H2606R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265077 |
| Start | 83520918:83520918(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2612A>G |
| AA Mutation | p.Glu871Gly(p.E871G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265077 |
| Start | 83538854:83538854(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5851G>A |
| AA Mutation | p.Glu1951Lys(p.E1951K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000265077 |
| Start | 83541136:83541136(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.8133T>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000265077 |
| Start | 83539210:83539210(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs563628544 |
| CDS Mutation | c.6207G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |