Primary Site >> Stomach Cancer
Gene >> KHDRBS3
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000355849 |
| Start | 135581931:135581931(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs150971318 |
| CDS Mutation | c.665C>T |
| AA Mutation | p.Thr222Met(p.T222M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000355849 |
| Start | 135542673:135542673(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.227T>C |
| AA Mutation | p.Leu76Pro(p.L76P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000355849 |
| Start | 135606996:135606996(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.849T>G |
| AA Mutation | p.Ser283Arg(p.S283R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000355849 |
| Start | 135645102:135645102(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.934A>G |
| AA Mutation | p.Thr312Ala(p.T312A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000355849 |
| Start | 135548840:135548840(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.411T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000355849 |
| Start | 135607011:135607011(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.864T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000355849 |
| Start | 135548885:135548885(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.456A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000355849 |
| Start | 135582061:135582061(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.795T>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000355849 |
| Start | 135557564:135557564(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.588T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000355849 |
| Start | 135645083:135645083(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.915A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000355849 |
| Start | 135582013:135582013(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs776179021 |
| CDS Mutation | c.752delC |
| AA Mutation | p.Pro251GlnfsTer101(p.P251Qfs*101) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |