Primary Site >> Stomach Cancer
Gene >> MYD88
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000396334 |
| Start | 38140839:38140839(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.766C>T |
| AA Mutation | p.Leu256Phe(p.L256F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000396334 |
| Start | 38139899:38139899(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.403C>G |
| AA Mutation | p.Gln135Glu(p.Q135E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000396334 |
| Start | 38140493:38140493(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.608A>C |
| AA Mutation | p.Lys203Thr(p.K203T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000396334 |
| Start | 38139954:38139954(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs781329078 |
| CDS Mutation | c.458G>A |
| AA Mutation | p.Arg153Gln(p.R153Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000396334 |
| Start | 38140451:38140451(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs764428425 |
| CDS Mutation | c.566A>G |
| AA Mutation | p.Gln189Arg(p.Q189R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000396334 |
| Start | 38139970:38139970(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs745818810 |
| CDS Mutation | c.474G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |