Primary Site >> Pancreatic Cancer
Gene >> GLI3
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000395925 |
| Start | 41978706:41978706(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs148502119 |
| CDS Mutation | c.1540G>A |
| AA Mutation | p.Val514Met(p.V514M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000395925 |
| Start | 41966108:41966108(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2965C>T |
| AA Mutation | p.Arg989Trp(p.R989W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000395925 |
| Start | 41972596:41972596(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1844C>G |
| AA Mutation | p.Thr615Ser(p.T615S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000395925 |
| Start | 41965922:41965922(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs767681231 |
| CDS Mutation | c.3151C>T |
| AA Mutation | p.Arg1051Trp(p.R1051W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000395925 |
| Start | 41965328:41965328(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3745T>G |
| AA Mutation | p.Cys1249Gly(p.C1249G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000395925 |
| Start | 41965701:41965701(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs542238121 |
| CDS Mutation | c.3372C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000395925 |
| Start | 42040208:42040208(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.858C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000395925 |
| Start | 41965329:41965329(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs776336534 |
| CDS Mutation | c.3744C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000395925 |
| Start | 41965683:41965683(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs756608797 |
| CDS Mutation | c.3390C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000395925 |
| Start | 41978684:41978684(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1562C>A |
| AA Mutation | p.Ser521Ter(p.S521*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |