Primary Site >> Stomach Cancer
Gene >> PADI4
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000375448 |
| Start | 17363662:17363662(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1899C>A |
| AA Mutation | p.Phe633Leu(p.F633L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000375448 |
| Start | 17339711:17339711(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.550A>G |
| AA Mutation | p.Thr184Ala(p.T184A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000375448 |
| Start | 17308274:17308274(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs371193672 |
| CDS Mutation | c.52G>A |
| AA Mutation | p.Val18Met(p.V18M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000375448 |
| Start | 17356119:17356119(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs142426054 |
| CDS Mutation | c.1447G>A |
| AA Mutation | p.Asp483Asn(p.D483N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000375448 |
| Start | 17363656:17363656(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs370827351 |
| CDS Mutation | c.1893C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000375448 |
| Start | 17308249:17308249(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.27G>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000375448 |
| Start | 17331005:17331005(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs138052968 |
| CDS Mutation | c.129C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000375448 |
| Start | 17339727:17339727(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.570delC |
| AA Mutation | p.Lys191ArgfsTer21(p.K191Rfs*21) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000375448 |
| Start | 17354572:17354572(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1199delG |
| AA Mutation | p.Gly400ValfsTer13(p.G400Vfs*13) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000375448 |
| Start | 17363556:17363557(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.1797dupC |
| AA Mutation | p.Lys600GlnfsTer113(p.K600Qfs*113) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |