Primary Site >> Pancreatic Cancer
Gene >> VCAN
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265077 |
| Start | 83522289:83522289(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3983A>G |
| AA Mutation | p.Glu1328Gly(p.E1328G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265077 |
| Start | 83483538:83483538(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.20G>T |
| AA Mutation | p.Ser7Ile(p.S7I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265077 |
| Start | 83490413:83490413(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs370476323 |
| CDS Mutation | c.386G>A |
| AA Mutation | p.Arg129His(p.R129H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265077 |
| Start | 83493881:83493881(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.698G>A |
| AA Mutation | p.Arg233His(p.R233H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265077 |
| Start | 83538887:83538887(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5884G>A |
| AA Mutation | p.Ala1962Thr(p.A1962T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265077 |
| Start | 83539592:83539592(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.6589C>A |
| AA Mutation | p.Pro2197Thr(p.P2197T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265077 |
| Start | 83541347:83541347(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.8344A>G |
| AA Mutation | p.Ile2782Val(p.I2782V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265077 |
| Start | 83540022:83540022(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.7019G>A |
| AA Mutation | p.Gly2340Glu(p.G2340E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265077 |
| Start | 83580355:83580355(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.10112C>T |
| AA Mutation | p.Ser3371Leu(p.S3371L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000265077 |
| Start | 83519587:83519587(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs144399722 |
| CDS Mutation | c.1281T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |