Primary Site >> Pancreatic Cancer
Gene >> MYH11
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000300036 |
| Start | 15748069:15748069(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs756408490 |
| CDS Mutation | c.2158G>A |
| AA Mutation | p.Val720Ile(p.V720I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000300036 |
| Start | 15720940:15720940(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs756121642 |
| CDS Mutation | c.4690C>T |
| AA Mutation | p.Arg1564Trp(p.R1564W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000300036 |
| Start | 15735577:15735577(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs757497342 |
| CDS Mutation | c.3295C>A |
| AA Mutation | p.Leu1099Ile(p.L1099I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000300036 |
| Start | 15747938:15747938(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2186A>C |
| AA Mutation | p.Glu729Ala(p.E729A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000300036 |
| Start | 15750292:15750292(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs745878375 |
| CDS Mutation | c.1904C>T |
| AA Mutation | p.Thr635Met(p.T635M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000300036 |
| Start | 15759659:15759659(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1318G>A |
| AA Mutation | p.Val440Met(p.V440M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000300036 |
| Start | 15732669:15732669(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3546C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000300036 |
| Start | 15837971:15837971(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs759914132 |
| CDS Mutation | c.282G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |