Primary Site >> Pancreatic Cancer
Gene >> VAV1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000602142 |
| Start | 6853977:6853977(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2363A>T |
| AA Mutation | p.Lys788Ile(p.K788I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000602142 |
| Start | 6820709:6820709(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.212G>A |
| AA Mutation | p.Cys71Tyr(p.C71Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000602142 |
| Start | 6828143:6828143(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.995G>A |
| AA Mutation | p.Arg332Gln(p.R332Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000602142 |
| Start | 6828881:6828881(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1246C>T |
| AA Mutation | p.Arg416Trp(p.R416W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000602142 |
| Start | 6836986:6836986(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1916G>A |
| AA Mutation | p.Gly639Asp(p.G639D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000602142 |
| Start | 6829840:6829840(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1320C>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000602142 |
| Start | 6828142:6828142(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.994C>T |
| AA Mutation | p.Arg332Ter(p.R332*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |