Primary Site >> Pancreatic Cancer
Gene >> TCF20
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359486 |
| Start | 42213318:42213318(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1988G>A |
| AA Mutation | p.Ser663Asn(p.S663N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359486 |
| Start | 42213748:42213748(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1558G>T |
| AA Mutation | p.Asp520Tyr(p.D520Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359486 |
| Start | 42209754:42209754(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5552A>G |
| AA Mutation | p.Glu1851Gly(p.E1851G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000359486 |
| Start | 42209780:42209780(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5526C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000359486 |
| Start | 42211433:42211433(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs369173064 |
| CDS Mutation | c.3873C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000359486 |
| Start | 42215240:42215240(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.66C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |