Primary Site >> Stomach Cancer
Gene >> CPA4
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000222482 |
| Start | 130306884:130306884(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.689A>G |
| AA Mutation | p.Tyr230Cys(p.Y230C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000222482 |
| Start | 130310837:130310837(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs570075096 |
| CDS Mutation | c.844G>A |
| AA Mutation | p.Ala282Thr(p.A282T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000222482 |
| Start | 130310980:130310980(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.987G>T |
| AA Mutation | p.Glu329Asp(p.E329D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000222482 |
| Start | 130322610:130322610(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1200C>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000222482 |
| Start | 130293236:130293236(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.60delA |
| AA Mutation | p.Lys20AsnfsTer8(p.K20Nfs*8) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000222482 |
| Start | 130310880:130310880(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs755208608 |
| CDS Mutation | c.891delA |
| AA Mutation | p.Lys297AsnfsTer18(p.K297Nfs*18) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000222482 |
| Start | 130308310:130308310(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs372059567 |
| CDS Mutation | c.706C>T |
| AA Mutation | p.Arg236Ter(p.R236*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |