Primary Site >> Esophagus Cancer
Gene >> VCAN
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265077 |
| Start | 83520686:83520686(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs772576243 |
| CDS Mutation | c.2380A>C |
| AA Mutation | p.Ser794Arg(p.S794R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265077 |
| Start | 83521217:83521217(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2911C>A |
| AA Mutation | p.His971Asn(p.H971N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265077 |
| Start | 83520850:83520850(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2544A>C |
| AA Mutation | p.Glu848Asp(p.E848D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265077 |
| Start | 83520759:83520759(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2453C>A |
| AA Mutation | p.Thr818Lys(p.T818K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265077 |
| Start | 83541986:83541986(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.8983A>T |
| AA Mutation | p.Ser2995Cys(p.S2995C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265077 |
| Start | 83512333:83512333(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.979C>T |
| AA Mutation | p.Arg327Cys(p.R327C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265077 |
| Start | 83541411:83541411(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.8408A>G |
| AA Mutation | p.Asn2803Ser(p.N2803S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000265077 |
| Start | 83542162:83542162(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.9159T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000265077 |
| Start | 83490402:83490402(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs762753715 |
| CDS Mutation | c.375G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000265077 |
| Start | 83522224:83522224(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs768841073 |
| CDS Mutation | c.3918G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000265077 |
| Start | 83519665:83519665(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1359A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000265077 |
| Start | 83545572:83545572(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.9301G>T |
| AA Mutation | p.Gly3101Ter(p.G3101*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |