Primary Site >> Stomach Cancer
Gene >> APIP
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000395787 |
| Start | 34883418:34883418(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.548A>G |
| AA Mutation | p.Glu183Gly(p.E183G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000395787 |
| Start | 34883467:34883467(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.499A>G |
| AA Mutation | p.Thr167Ala(p.T167A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000395787 |
| Start | 34895101:34895101(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.67C>T |
| AA Mutation | p.His23Tyr(p.H23Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000395787 |
| Start | 34895034:34895034(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.134G>A |
| AA Mutation | p.Gly45Glu(p.G45E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000395787 |
| Start | 34888794:34888794(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs768283418 |
| CDS Mutation | c.283delA |
| AA Mutation | p.Ser95AlafsTer8(p.S95Afs*8) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000395787 |
| Start | 34883362:34883362(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.604delG |
| AA Mutation | p.Glu202LysfsTer23(p.E202Kfs*23) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |