Primary Site >> Stomach Cancer
Gene >> AMT
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000273588 |
| Start | 49422422:49422422(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs150649086 |
| CDS Mutation | c.29G>A |
| AA Mutation | p.Arg10His(p.R10H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000273588 |
| Start | 49422398:49422398(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.53T>C |
| AA Mutation | p.Phe18Ser(p.F18S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000273588 |
| Start | 49417681:49417681(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1071G>T |
| AA Mutation | p.Lys357Asn(p.K357N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000273588 |
| Start | 49422366:49422366(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.85G>A |
| AA Mutation | p.Ala29Thr(p.A29T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000273588 |
| Start | 49420319:49420319(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs367604855 |
| CDS Mutation | c.363C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000273588 |
| Start | 49419062:49419062(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.786delC |
| AA Mutation | p.Asp262GlufsTer51(p.D262Efs*51) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |