Primary Site >> Stomach Cancer
Gene >> APAF1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000551964 |
| Start | 98708696:98708696(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs774076296 |
| CDS Mutation | c.2833C>T |
| AA Mutation | p.Arg945Cys(p.R945C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000551964 |
| Start | 98686831:98686831(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2262T>G |
| AA Mutation | p.Asp754Glu(p.D754E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000551964 |
| Start | 98665778:98665778(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1181A>C |
| AA Mutation | p.Lys394Thr(p.K394T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000551964 |
| Start | 98683207:98683207(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2111G>A |
| AA Mutation | p.Cys704Tyr(p.C704Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000551964 |
| Start | 98648791:98648791(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.304T>G |
| AA Mutation | p.Ser102Ala(p.S102A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000551964 |
| Start | 98732492:98732492(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201029707 |
| CDS Mutation | c.3673G>A |
| AA Mutation | p.Val1225Met(p.V1225M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000551964 |
| Start | 98683251:98683251(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2155G>A |
| AA Mutation | p.Gly719Arg(p.G719R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000551964 |
| Start | 98712334:98712334(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs763464521 |
| CDS Mutation | c.2857A>G |
| AA Mutation | p.Thr953Ala(p.T953A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000551964 |
| Start | 98699419:98699419(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs368374940 |
| CDS Mutation | c.2316G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |