| Variant ID | 18583 |
|---|---|
| Entrez Gene ID | 79820 |
| Gene | CATSPERB (GeneCards) |
| Location | hg19 14:92143637-92143637
hg38 14:91677293-91677293 |
| Disease | Cockayne syndrome (view all the variants in this disease) |
| Method | HiSeq X Ten |
| Mutation(HGVS format) | NC_000014.8:g.92143637 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 | 107349540 |
| MAF in gnomAD genome (version 2.0.1) | 0.0002 |
|---|---|
| EIGEN score | -0.3399 |
| CADD Raw score (version 1.3) | -0.2189 (Deleterious) |
| FATHMM raw prediction score | 0.07704 (Tolerated) |
| Deleterious probability by DeFine | 0.089 (Neutral) |
| Entrez Gene ID | 79820 (NCBI Gene) |
|---|---|
| Official Gene Symbol | CATSPERB (GeneCards) |
| Number of variants in CATSPERB in this database | 2 (view all the variants) |
| Full name | cation channel sperm associated auxiliary subunit beta |
| Band | 14q32.12 |
| Other IDs | Vega: OTTHUMG00000171118 OMIM: 611169 HGNC: HGNC:20500 Ensembl: ENSG00000133962 |
| Other names | C14orf161, CatSper(beta) |
| Summary | None |
| Individual ID | 29217584.16 (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; |