Primary Site >> Pancreatic Cancer
Gene >> MAML1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000292599 |
| Start | 179765578:179765578(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs766359390 |
| CDS Mutation | c.568C>T |
| AA Mutation | p.Arg190Cys(p.R190C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000292599 |
| Start | 179766166:179766166(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs769816363 |
| CDS Mutation | c.1156G>A |
| AA Mutation | p.Gly386Ser(p.G386S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000292599 |
| Start | 179766308:179766308(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs199501746 |
| CDS Mutation | c.1298C>T |
| AA Mutation | p.Thr433Met(p.T433M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000292599 |
| Start | 179766072:179766072(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1062C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000292599 |
| Start | 179774460:179774460(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2634C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000292599 |
| Start | 179774851:179774851(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3025T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |