Primary Site >> Pancreatic Cancer
Gene >> WWC1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265293 |
| Start | 168385297:168385297(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.316G>A |
| AA Mutation | p.Ala106Thr(p.A106T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265293 |
| Start | 168423792:168423792(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1534G>A |
| AA Mutation | p.Ala512Thr(p.A512T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265293 |
| Start | 168464802:168464802(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs527539467 |
| CDS Mutation | c.2990C>T |
| AA Mutation | p.Ala997Val(p.A997V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000265293 |
| Start | 168406201:168406201(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs767253675 |
| CDS Mutation | c.594C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000265293 |
| Start | 168455439:168455439(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2742C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000265293 |
| Start | 168454058:168454058(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs771813160 |
| CDS Mutation | c.2616C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |