Primary Site >> Stomach Cancer
Gene >> SERPINF2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000324015 |
| Start | 1747053:1747053(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.402G>T |
| AA Mutation | p.Gln134His(p.Q134H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000324015 |
| Start | 1754242:1754242(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs752766333 |
| CDS Mutation | c.1184C>T |
| AA Mutation | p.Ala395Val(p.A395V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000324015 |
| Start | 1747368:1747368(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs767167105 |
| CDS Mutation | c.571G>A |
| AA Mutation | p.Val191Met(p.V191M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000324015 |
| Start | 1754170:1754170(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1112A>G |
| AA Mutation | p.Gln371Arg(p.Q371R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000324015 |
| Start | 1754271:1754271(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1213T>C |
| AA Mutation | p.Ser405Pro(p.S405P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000324015 |
| Start | 1747485:1747485(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.688C>T |
| AA Mutation | p.Leu230Phe(p.L230F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000324015 |
| Start | 1745819:1745819(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs747689438 |
| CDS Mutation | c.277C>A |
| AA Mutation | p.Leu93Met(p.L93M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000324015 |
| Start | 1754318:1754318(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs147941157 |
| CDS Mutation | c.1260C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |