| Variant ID | 4680 |
|---|---|
| Entrez Gene ID | 53833 |
| Gene | IL20RB (GeneCards) |
| Location | hg19 3:136864166-136864166
hg38 3:137145324-137145324 |
| Disease | Asymptomatic |
| Method | HiSeq X Ten |
| Mutation(HGVS format) | NC_000003.11:g.136864166 C>T (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 | 198022430 |
| MAF in gnomAD genome (version 2.0.1) | 0 |
|---|---|
| EIGEN score | -0.2522 |
| CADD Raw score (version 1.3) | -0.024806 (Deleterious) |
| FATHMM raw prediction score | 0.10137 (Tolerated) |
| Deleterious probability by DeFine | 0.1989 (Neutral) |
| Entrez Gene ID | 53833 (NCBI Gene) |
|---|---|
| Official Gene Symbol | IL20RB (GeneCards) |
| Number of variants in IL20RB in this database | 9 (view all the variants) |
| Full name | interleukin 20 receptor subunit beta |
| Band | 3q22.3 |
| Other IDs | Vega: OTTHUMG00000159779 OMIM: 605621 HGNC: HGNC:6004 Ensembl: ENSG00000174564 |
| Other names | DIRS1, FNDC6, IL-20R2 |
| Summary | IL20RB and IL20RA (MIM 605620) form a heterodimeric receptor for interleukin-20 (IL20; MIM 605619) (Blumberg et al., 2001 [PubMed 11163236]).[supplied by OMIM, Feb 2009] |
| Individual ID | 29217584.03 (view all the variants in this individual) |
|---|---|
| Pubmed ID | 29217584 |
| Whose mosaic mutation | Normal |
| Phenotype | 1 |
| Disease | Asymptomatic |
| OMIM ID |
| 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; |