Primary Site >> Stomach Cancer
Gene >> VAV3
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000370056 |
| Start | 107609962:107609962(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1984C>T |
| AA Mutation | p.Pro662Ser(p.P662S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000370056 |
| Start | 107964842:107964842(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.28T>C |
| AA Mutation | p.Trp10Arg(p.W10R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000370056 |
| Start | 107642708:107642708(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1825C>T |
| AA Mutation | p.Pro609Ser(p.P609S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000370056 |
| Start | 107874946:107874946(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.276A>C |
| AA Mutation | p.Glu92Asp(p.E92D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000370056 |
| Start | 107760813:107760813(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs764254114 |
| CDS Mutation | c.988C>T |
| AA Mutation | p.Arg330Cys(p.R330C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000370056 |
| Start | 107574162:107574162(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs142668144 |
| CDS Mutation | c.2387G>A |
| AA Mutation | p.Arg796Gln(p.R796Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000370056 |
| Start | 107596331:107596331(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2231A>T |
| AA Mutation | p.Glu744Val(p.E744V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000370056 |
| Start | 107755450:107755450(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1150T>G |
| AA Mutation | p.Phe384Val(p.F384V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000370056 |
| Start | 107573351:107573351(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2524T>C |
| AA Mutation | p.Tyr842His(p.Y842H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000370056 |
| Start | 107704613:107704613(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1642G>A |
| AA Mutation | p.Gly548Arg(p.G548R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000370056 |
| Start | 107779458:107779458(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.356C>T |
| AA Mutation | p.Pro119Leu(p.P119L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000370056 |
| Start | 107875001:107875001(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.221A>G |
| AA Mutation | p.Asn74Ser(p.N74S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000370056 |
| Start | 107765163:107765163(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201515652 |
| CDS Mutation | c.834C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000370056 |
| Start | 107574167:107574167(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200778284 |
| CDS Mutation | c.2382C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |