Primary Site >> Pancreatic Cancer
Gene >> EP400
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389562 |
| Start | 132043697:132043697(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.6419C>T |
| AA Mutation | p.Ser2140Phe(p.S2140F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389562 |
| Start | 131982198:131982198(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1649T>C |
| AA Mutation | p.Leu550Ser(p.L550S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000389562 |
| Start | 131991453:131991453(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2676T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000389562 |
| Start | 132013520:132013520(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs764523068 |
| CDS Mutation | c.3642G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000389562 |
| Start | 132017556:132017556(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs540244111 |
| CDS Mutation | c.3945C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000389562 |
| Start | 132064724:132064724(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs144085795 |
| CDS Mutation | c.8391G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000389562 |
| Start | 132069524:132069524(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs752684673 |
| CDS Mutation | c.8904C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000389562 |
| Start | 132077433:132077433(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.9132G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000389562 |
| Start | 132032108:132032108(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5910G>A |
| AA Mutation | p.Trp1970Ter(p.W1970*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |