Primary Site >> Liver Cancer
Gene >> RECQL4
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000617875 |
| Start | 144515334:144515334(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1382A>T |
| AA Mutation | p.Gln461Leu(p.Q461L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000617875 |
| Start | 144512948:144512948(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2654T>C |
| AA Mutation | p.Leu885Pro(p.L885P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000617875 |
| Start | 144516371:144516371(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.748G>C |
| AA Mutation | p.Gly250Arg(p.G250R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000617875 |
| Start | 144514100:144514100(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs761794554 |
| CDS Mutation | c.1886G>A |
| AA Mutation | p.Arg629Gln(p.R629Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000617875 |
| Start | 144511928:144511928(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs779826649 |
| CDS Mutation | c.3376G>A |
| AA Mutation | p.Glu1126Lys(p.E1126K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000617875 |
| Start | 144515042:144515042(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1514G>C |
| AA Mutation | p.Gly505Ala(p.G505A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000617875 |
| Start | 144514461:144514461(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs375562152 |
| CDS Mutation | c.1685G>A |
| AA Mutation | p.Arg562Gln(p.R562Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000617875 |
| Start | 144513329:144513329(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2352G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000617875 |
| Start | 144511736:144511736(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3447G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000617875 |
| Start | 144513395:144513395(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2286G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |