Primary Site >> Pancreatic Cancer
Gene >> MYH10
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000269243 |
| Start | 8476984:8476984(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs778680463 |
| CDS Mutation | c.5678C>T |
| AA Mutation | p.Ala1893Val(p.A1893V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000269243 |
| Start | 8542169:8542169(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1513G>A |
| AA Mutation | p.Glu505Lys(p.E505K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000269243 |
| Start | 8545533:8545533(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs768634600 |
| CDS Mutation | c.1316G>A |
| AA Mutation | p.Arg439His(p.R439H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000269243 |
| Start | 8495193:8495193(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3907G>T |
| AA Mutation | p.Gly1303Cys(p.G1303C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000269243 |
| Start | 8478362:8478362(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5589A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000269243 |
| Start | 8487487:8487487(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs375050384 |
| CDS Mutation | c.4899C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |