Primary Site >> Pancreatic Cancer
Gene >> TRPM6
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360774 |
| Start | 74762079:74762079(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs199963114 |
| CDS Mutation | c.4592G>A |
| AA Mutation | p.Arg1531His(p.R1531H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360774 |
| Start | 74808095:74808095(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1577G>A |
| AA Mutation | p.Arg526His(p.R526H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360774 |
| Start | 74802010:74802010(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1897G>A |
| AA Mutation | p.Glu633Lys(p.E633K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360774 |
| Start | 74808071:74808071(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1601T>G |
| AA Mutation | p.Phe534Cys(p.F534C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360774 |
| Start | 74816747:74816747(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1230G>T |
| AA Mutation | p.Glu410Asp(p.E410D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000360774 |
| Start | 74801984:74801984(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs372508531 |
| CDS Mutation | c.1923G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000360774 |
| Start | 74762306:74762306(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4365G>A |
| AA Mutation | p.Trp1455Ter(p.W1455*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000360774 |
| Start | 74812361:74812361(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1381G>T |
| AA Mutation | p.Glu461Ter(p.E461*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |