Primary Site >> Stomach Cancer
Gene >> AFM
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000226355 |
| Start | 73486034:73486034(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.443G>A |
| AA Mutation | p.Cys148Tyr(p.C148Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000226355 |
| Start | 73491956:73491956(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs536766988 |
| CDS Mutation | c.928C>T |
| AA Mutation | p.Arg310Cys(p.R310C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000226355 |
| Start | 73488752:73488752(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs149021212 |
| CDS Mutation | c.836G>A |
| AA Mutation | p.Arg279His(p.R279H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000226355 |
| Start | 73499215:73499215(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1391T>C |
| AA Mutation | p.Leu464Pro(p.L464P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000226355 |
| Start | 73486014:73486014(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.423C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000226355 |
| Start | 73501805:73501805(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1665G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000226355 |
| Start | 73481814:73481815(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | rs561835861 |
| CDS Mutation | c.47dupT |
| AA Mutation | p.Leu16PhefsTer3(p.L16Ffs*3) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |