Overview

Variant ID 13782
Entrez Gene ID 3293
Gene HSD17B3 (GeneCards)
Location hg19 9:99079352-99079352
hg38 9:96317070-96317070
Disease Xeroderma Pigmentosum (view all the variants in this disease)
Method HiSeq X Ten
Mutation(HGVS format) NC_000009.11:g.99079352 G>A (Genome Assembly: GRCh37)

Other information

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 141213431

Annotations and predictions

MAF in gnomAD genome (version 2.0.1) 0.00003259
EIGEN score -0.506
CADD Raw score (version 1.3) -0.388073 (Deleterious)
FATHMM raw prediction score 0.04561 (Tolerated)
Deleterious probability by DeFine 0.1324 (Neutral)
Entrez Gene ID 3293 (NCBI Gene)
Official Gene Symbol HSD17B3 (GeneCards)
Number of variants in HSD17B3 in this database 6 (view all the variants)
Full name hydroxysteroid 17-beta dehydrogenase 3
Band 9q22.32
Other IDs Vega: OTTHUMG00000020292
OMIM: 605573
HGNC: HGNC:5212
Ensembl: ENSG00000130948
Other names EDH17B3, SDR12C2
Summary This isoform of 17 beta-hydroxysteroid dehydrogenase is expressed predominantly in the testis and catalyzes the conversion of androstenedione to testosterone. It preferentially uses NADP as cofactor. Deficiency can result in male pseudohermaphroditism with gynecomastia. [provided by RefSeq, Jul 2008]

Individual #1

Individual ID 29217584.23 (view all the variants in this individual)
Pubmed ID 29217584
Whose mosaic mutation Female Patient  
Phenotype 3  
Disease Xeroderma Pigmentosum (view all the variants in this disease)
OMIM ID 278700

Publication #1: 29217584

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;