Primary Site >> Pancreatic Cancer
Gene >> TRPM1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397795 |
| Start | 31031033:31031033(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3011A>G |
| AA Mutation | p.Tyr1004Cys(p.Y1004C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397795 |
| Start | 31042145:31042145(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1827G>T |
| AA Mutation | p.Gln609His(p.Q609H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397795 |
| Start | 31070096:31070096(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.148A>C |
| AA Mutation | p.Ser50Arg(p.S50R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397795 |
| Start | 31026924:31026924(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs763463725 |
| CDS Mutation | c.3421C>T |
| AA Mutation | p.Arg1141Cys(p.R1141C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397795 |
| Start | 31042155:31042155(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1817G>T |
| AA Mutation | p.Ser606Ile(p.S606I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000397795 |
| Start | 31050487:31050487(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1293delG |
| AA Mutation | p.Gly433AlafsTer7(p.G433Afs*7) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | splice_donor_variant |
| Transcription ID | ENST00000397795 |
| Start | 31037710:31037710(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2505+1G>T |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |