Primary Site >> Liver Cancer
Gene >> SUPT20H
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000350612 |
| Start | 37031798:37031798(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.805A>G |
| AA Mutation | p.Lys269Glu(p.K269E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000350612 |
| Start | 37009677:37009677(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2335T>C |
| AA Mutation | p.Phe779Leu(p.F779L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000350612 |
| Start | 37045346:37045346(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.193G>A |
| AA Mutation | p.Glu65Lys(p.E65K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000350612 |
| Start | 37009767:37009767(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs766826291 |
| CDS Mutation | c.2245G>A |
| AA Mutation | p.Ala749Thr(p.A749T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000350612 |
| Start | 37025405:37025405(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs768205505 |
| CDS Mutation | c.1244A>G |
| AA Mutation | p.Asn415Ser(p.N415S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000350612 |
| Start | 37047576:37047576(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs530162287 |
| CDS Mutation | c.124G>T |
| AA Mutation | p.Asp42Tyr(p.D42Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |