Primary Site >> Pancreatic Cancer
Gene >> TJP1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000346128 |
| Start | 29710934:29710934(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4269G>T |
| AA Mutation | p.Gln1423His(p.Q1423H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000346128 |
| Start | 29718727:29718727(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs141258029 |
| CDS Mutation | c.3415T>C |
| AA Mutation | p.Ser1139Pro(p.S1139P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000346128 |
| Start | 29718815:29718815(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3327G>T |
| AA Mutation | p.Gln1109His(p.Q1109H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000346128 |
| Start | 29719804:29719804(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2976A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000346128 |
| Start | 29728008:29728008(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2029C>T |
| AA Mutation | p.Arg677Ter(p.R677*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | splice_acceptor_variant |
| Transcription ID | ENST00000346128 |
| Start | 29773358:29773358(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.85-1G>T |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |