Primary Site >> Liver Cancer
Gene >> GLI3
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000395925 |
| Start | 41967661:41967661(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2366T>A |
| AA Mutation | p.Met789Lys(p.M789K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000395925 |
| Start | 41977602:41977602(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1768G>T |
| AA Mutation | p.Ala590Ser(p.A590S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000395925 |
| Start | 41964754:41964754(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4319C>A |
| AA Mutation | p.Ser1440Tyr(p.S1440Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000395925 |
| Start | 42026384:42026384(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs375277249 |
| CDS Mutation | c.1057G>A |
| AA Mutation | p.Ala353Thr(p.A353T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000395925 |
| Start | 41972357:41972357(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs199606102 |
| CDS Mutation | c.2083G>A |
| AA Mutation | p.Val695Ile(p.V695I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000395925 |
| Start | 41965432:41965432(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3641A>C |
| AA Mutation | p.Gln1214Pro(p.Q1214P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000395925 |
| Start | 41966111:41966111(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs765236732 |
| CDS Mutation | c.2962G>A |
| AA Mutation | p.Gly988Arg(p.G988R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000395925 |
| Start | 42048602:42048602(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.568T>A |
| AA Mutation | p.Phe190Ile(p.F190I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000395925 |
| Start | 42045506:42045506(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.704C>G |
| AA Mutation | p.Ala235Gly(p.A235G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000395925 |
| Start | 42076819:42076819(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.406C>A |
| AA Mutation | p.Pro136Thr(p.P136T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000395925 |
| Start | 42223149:42223149(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.105C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000395925 |
| Start | 41977711:41977711(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs532041527 |
| CDS Mutation | c.1659C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |