Primary Site >> Stomach Cancer
Gene >> APOA1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000236850 |
| Start | 116836358:116836358(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.254G>A |
| AA Mutation | p.Arg85His(p.R85H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000236850 |
| Start | 116836094:116836094(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.518G>A |
| AA Mutation | p.Arg173His(p.R173H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000236850 |
| Start | 116835846:116835846(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.766G>T |
| AA Mutation | p.Ala256Ser(p.A256S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000236850 |
| Start | 116836083:116836083(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.529C>T |
| AA Mutation | p.Arg177Cys(p.R177C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000236850 |
| Start | 116837011:116837011(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.190A>G |
| AA Mutation | p.Lys64Glu(p.K64E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000236850 |
| Start | 116837377:116837377(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.11C>T |
| AA Mutation | p.Ala4Val(p.A4V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000236850 |
| Start | 116835888:116835888(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.724C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000236850 |
| Start | 116836084:116836084(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.528G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000236850 |
| Start | 116836297:116836297(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs148950234 |
| CDS Mutation | c.315C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |