Primary Site >> Pancreatic Cancer
Gene >> GLI1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000228682 |
| Start | 57465815:57465815(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.652C>T |
| AA Mutation | p.Arg218Trp(p.R218W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000228682 |
| Start | 57468087:57468087(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs764631331 |
| CDS Mutation | c.1171G>A |
| AA Mutation | p.Ala391Thr(p.A391T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000228682 |
| Start | 57465888:57465888(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.725G>A |
| AA Mutation | p.Cys242Tyr(p.C242Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000228682 |
| Start | 57466316:57466316(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.839G>T |
| AA Mutation | p.Arg280Met(p.R280M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000228682 |
| Start | 57470464:57470464(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1724C>T |
| AA Mutation | p.Ala575Val(p.A575V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000228682 |
| Start | 57470723:57470723(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1983C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |