Primary Site >> Stomach Cancer
Gene >> BPIFA1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000354297 |
| Start | 33240366:33240366(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs115425643 |
| CDS Mutation | c.562C>A |
| AA Mutation | p.Gln188Lys(p.Q188K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000354297 |
| Start | 33238180:33238180(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.286A>G |
| AA Mutation | p.Thr96Ala(p.T96A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000354297 |
| Start | 33237720:33237720(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.9A>C |
| AA Mutation | p.Gln3His(p.Q3H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000354297 |
| Start | 33241455:33241455(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.652T>G |
| AA Mutation | p.Leu218Val(p.L218V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000354297 |
| Start | 33241460:33241460(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.657T>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000354297 |
| Start | 33237858:33237858(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.147A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000354297 |
| Start | 33238110:33238110(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs143582801 |
| CDS Mutation | c.216G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |