Primary Site >> Stomach Cancer
Gene >> CASP4
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000444739 |
| Start | 104950965:104950965(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.506T>C |
| AA Mutation | p.Leu169Pro(p.L169P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000444739 |
| Start | 104949648:104949648(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs138280041 |
| CDS Mutation | c.676C>A |
| AA Mutation | p.Pro226Thr(p.P226T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000444739 |
| Start | 104951041:104951041(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.430A>G |
| AA Mutation | p.Thr144Ala(p.T144A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000444739 |
| Start | 104948533:104948533(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs745951817 |
| CDS Mutation | c.925C>T |
| AA Mutation | p.His309Tyr(p.H309Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000444739 |
| Start | 104947094:104947094(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1024G>T |
| AA Mutation | p.Val342Leu(p.V342L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000444739 |
| Start | 104949747:104949747(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs559503139 |
| CDS Mutation | c.577A>G |
| AA Mutation | p.Thr193Ala(p.T193A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000444739 |
| Start | 104954904:104954904(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.105G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000444739 |
| Start | 104954868:104954868(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.141T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000444739 |
| Start | 104954881:104954881(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs772291949 |
| CDS Mutation | c.128delA |
| AA Mutation | p.Lys43ArgfsTer37(p.K43Rfs*37) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000444739 |
| Start | 104954778:104954778(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs779092072 |
| CDS Mutation | c.231delT |
| AA Mutation | p.Phe77LeufsTer3(p.F77Lfs*3) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | splice_acceptor_variant |
| Transcription ID | ENST00000444739 |
| Start | 104955002:104955002(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200174319 |
| CDS Mutation | c.8-1G>A |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |