Primary Site >> Liver Cancer
Gene >> SREBF2
| ID | 1 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000361204 |
| Start | 41877942:41877942(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1580G>T |
| AA Mutation | p.Gly527Val(p.G527V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361204 |
| Start | 41877338:41877338(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1496C>G |
| AA Mutation | p.Ser499Cys(p.S499C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361204 |
| Start | 41875602:41875602(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs751254073 |
| CDS Mutation | c.1264G>A |
| AA Mutation | p.Glu422Lys(p.E422K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361204 |
| Start | 41873975:41873975(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1045A>G |
| AA Mutation | p.Lys349Glu(p.K349E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000361204 |
| Start | 41870954:41870954(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.786C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000361204 |
| Start | 41884870:41884870(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200493376 |
| CDS Mutation | c.2067C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |