Primary Site >> Stomach Cancer
Gene >> VAV2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371850 |
| Start | 133939197:133939197(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.227G>A |
| AA Mutation | p.Arg76His(p.R76H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371850 |
| Start | 133795702:133795702(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1067G>T |
| AA Mutation | p.Arg356Met(p.R356M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371850 |
| Start | 133785876:133785876(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs186434110 |
| CDS Mutation | c.1432G>A |
| AA Mutation | p.Gly478Ser(p.G478S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371850 |
| Start | 133791839:133791839(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs142018797 |
| CDS Mutation | c.1132C>T |
| AA Mutation | p.Arg378Trp(p.R378W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371850 |
| Start | 133797723:133797723(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.923G>A |
| AA Mutation | p.Arg308Lys(p.R308K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371850 |
| Start | 133778806:133778806(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs747112648 |
| CDS Mutation | c.1846G>A |
| AA Mutation | p.Val616Met(p.V616M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371850 |
| Start | 133788362:133788362(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1399G>A |
| AA Mutation | p.Val467Ile(p.V467I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371850 |
| Start | 133770395:133770395(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2330C>T |
| AA Mutation | p.Ala777Val(p.A777V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371850 |
| Start | 133809065:133809065(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs754228976 |
| CDS Mutation | c.641A>G |
| AA Mutation | p.Tyr214Cys(p.Y214C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371850 |
| Start | 133778874:133778874(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1778C>T |
| AA Mutation | p.Ala593Val(p.A593V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000371850 |
| Start | 133771971:133771971(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs543238251 |
| CDS Mutation | c.2211C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000371850 |
| Start | 133812177:133812177(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs751379406 |
| CDS Mutation | c.489G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000371850 |
| Start | 133861421:133861421(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs550293191 |
| CDS Mutation | c.333G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000371850 |
| Start | 133812183:133812183(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs755564188 |
| CDS Mutation | c.483C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |