Variant ID | 14856 |
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Entrez Gene ID | 105 |
Gene | ADARB2 (GeneCards) |
Location | hg19 10:1360542-1360542
hg38 10:1318347-1318347 |
Disease | Xeroderma Pigmentosum (view all the variants in this disease) |
Method | HiSeq X Ten |
Mutation(HGVS format) | NC_000010.10:g.1360542 T>C (Genome Assembly: GRCh37) |
Exon or Intron | NA |
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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 | 135534747 |
MAF in gnomAD genome (version 2.0.1) | 0 |
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EIGEN score | 0.1458 |
CADD Raw score (version 1.3) | 0.119733 (Deleterious) |
FATHMM raw prediction score | 0.26571 (Tolerated) |
Deleterious probability by DeFine | 0.6291 (Deleterious) |
Entrez Gene ID | 105 (NCBI Gene) |
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Official Gene Symbol | ADARB2 (GeneCards) |
Number of variants in ADARB2 in this database | 19 (view all the variants) |
Full name | adenosine deaminase, RNA specific B2 (inactive) |
Band | 10p15.3 |
Other IDs | Vega: OTTHUMG00000017543 OMIM: 602065 HGNC: HGNC:227 Ensembl: ENSG00000185736 |
Other names | RED2, ADAR3 |
Summary | This gene encodes a member of the double-stranded RNA adenosine deaminase family of RNA-editing enzymes and may play a regulatory role in RNA editing. [provided by RefSeq, Jul 2008] |
Individual ID | 29217584.22 (view all the variants in this individual) |
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Pubmed ID | 29217584 |
Whose mosaic mutation | Female Patient |
Phenotype | 3 |
Disease | Xeroderma Pigmentosum (view all the variants in this disease) |
OMIM ID | 278700 |
Pubmed ID | 29217584 |
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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; |