| Variant ID | 15877 |
|---|---|
| Entrez Gene ID | 65975 |
| Gene | STK33 (GeneCards) |
| Location | hg19 11:8596386-8596386
hg38 11:8574839-8574839 |
| Disease | Cockayne syndrome (view all the variants in this disease) |
| Method | HiSeq X Ten |
| Mutation(HGVS format) | NC_000011.9:g.8596386 G>A (Genome Assembly: GRCh37) |
| Exon or Intron | NA |
|---|---|
| Position in protein | NA |
| Amino acid changes in protein | NA > NA |
| Position in cDNA | NA |
| Changes in cDNA | NA > NA |
| mRNA accession | NA |
| mRNA length | NA |
| Reference length | 135006516 |
| MAF in gnomAD genome (version 2.0.1) | 0 |
|---|---|
| EIGEN score | -0.774 |
| CADD Raw score (version 1.3) | -0.708615 (Deleterious) |
| FATHMM raw prediction score | 0.08044 (Tolerated) |
| Deleterious probability by DeFine | 0.2016 (Neutral) |
| Entrez Gene ID | 65975 (NCBI Gene) |
|---|---|
| Official Gene Symbol | STK33 (GeneCards) |
| Number of variants in STK33 in this database | 4 (view all the variants) |
| Full name | serine/threonine kinase 33 |
| Band | 11p15.4 |
| Other IDs | Vega: OTTHUMG00000140275 OMIM: 607670 HGNC: HGNC:14568 Ensembl: ENSG00000130413 |
| Other names | None |
| Summary | None |
| Individual ID | 29217584.19 (view all the variants in this individual) |
|---|---|
| Pubmed ID | 29217584 |
| Whose mosaic mutation | Female Patient |
| Phenotype | 3 |
| Disease | Cockayne syndrome (view all the variants in this disease) |
| OMIM ID | 216400 |
| Pubmed ID | 29217584 |
|---|---|
| Title | Aging and neurodegeneration are associated with increased mutations in single human neurons. |
| Journal | Science |
| Publication date | 2018.02 |
| Disease | Cockayne syndrome Xeroderma Pigmentosum |
| Number of cases | Male cases: 3; Female cases: 6; cases of unknown sex: 15; |