Primary Site >> Pancreatic Cancer
Gene >> CTNNB1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000349496 |
| Start | 41224645:41224645(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs121913407 |
| CDS Mutation | c.133T>C |
| AA Mutation | p.Ser45Pro(p.S45P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000349496 |
| Start | 41236401:41236401(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1856G>A |
| AA Mutation | p.Cys619Tyr(p.C619Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000349496 |
| Start | 41225131:41225131(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.419T>A |
| AA Mutation | p.Ile140Asn(p.I140N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000349496 |
| Start | 41233531:41233531(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs751375496 |
| CDS Mutation | c.1188A>C |
| AA Mutation | p.Glu396Asp(p.E396D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000349496 |
| Start | 41233586:41233586(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1243A>C |
| AA Mutation | p.Asn415His(p.N415H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000349496 |
| Start | 41233605:41233605(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1262C>T |
| AA Mutation | p.Ala421Val(p.A421V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000349496 |
| Start | 41234239:41234239(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs551257843 |
| CDS Mutation | c.1625G>A |
| AA Mutation | p.Arg542His(p.R542H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000349496 |
| Start | 41224633:41224633(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs121913412 |
| CDS Mutation | c.121A>G |
| AA Mutation | p.Thr41Ala(p.T41A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |