Primary Site >> Stomach Cancer
Gene >> SYK
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000375746 |
| Start | 90877741:90877741(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1352C>T |
| AA Mutation | p.Ala451Val(p.A451V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000375746 |
| Start | 90844152:90844152(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.254C>A |
| AA Mutation | p.Pro85His(p.P85H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000375746 |
| Start | 90877753:90877753(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1364C>T |
| AA Mutation | p.Pro455Leu(p.P455L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000375746 |
| Start | 90844172:90844172(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.274C>T |
| AA Mutation | p.His92Tyr(p.H92Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000375746 |
| Start | 90874219:90874219(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.931G>A |
| AA Mutation | p.Gly311Arg(p.G311R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000375746 |
| Start | 90862282:90862282(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.655G>A |
| AA Mutation | p.Asp219Asn(p.D219N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000375746 |
| Start | 90877731:90877731(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1342A>T |
| AA Mutation | p.Met448Leu(p.M448L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000375746 |
| Start | 90888598:90888598(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs770904726 |
| CDS Mutation | c.1806C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000375746 |
| Start | 90887784:90887784(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201650753 |
| CDS Mutation | c.1617C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000375746 |
| Start | 90874712:90874712(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs142936514 |
| CDS Mutation | c.1044C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |