Overview

Variant ID 26222
Entrez Gene ID 51302
Gene CYP39A1 (GeneCards)
Location hg19 6:46548168-46548168
hg38 6:46580431-46580431
Disease Asymptomatic
Method Single cell Sequencing Cell cloning
Mutation(HGVS format) NC_000006.11:g.46548168 G>T (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 171115067

Annotations and predictions

MAF in gnomAD genome (version 2.0.1) 0
EIGEN score -0.299
CADD Raw score (version 1.3) -0.199416 (Deleterious)
FATHMM raw prediction score 0.07304 (Tolerated)
Deleterious probability by DeFine 0.051 (Neutral)
Entrez Gene ID 51302 (NCBI Gene)
Official Gene Symbol CYP39A1 (GeneCards)
Number of variants in CYP39A1 in this database 2 (view all the variants)
Full name cytochrome P450 family 39 subfamily A member 1
Band 6p12.3
Other IDs Vega: OTTHUMG00000014785
OMIM: 605994
HGNC: HGNC:17449
Ensembl: ENSG00000146233
Other names None
Summary This gene encodes a member of the cytochrome P450 superfamily of enzymes. The cytochrome P450 proteins are monooxygenases which catalyze many reactions involved in drug metabolism and synthesis of cholesterol, steroids and other lipids. This endoplasmic reticulum protein is involved in the conversion of cholesterol to bile acids. Its substrates include the oxysterols 25-hydroxycholesterol, 27-hydroxycholesterol and 24-hydroxycholesterol. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Jul 2013]

Individual #1

Individual ID 29217587.03 (view all the variants in this individual)
Pubmed ID 29217587
Whose mosaic mutation Normal  
Phenotype 1  
Disease Asymptomatic
OMIM ID