Overview

Variant ID 20827
Entrez Gene ID 8529
Gene CYP4F2 (GeneCards)
Location hg19 19:16008276-16008276
hg38 19:15897466-15897466
Disease Asymptomatic
Method HiSeq 2000
Mutation(HGVS format) NC_000019.9:g.16008276 C>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 59128983

Annotations and predictions

MAF in gnomAD genome (version 2.0.1) 0.0002
SNP ID (dbSNP ID version 137) rs201380574
EIGEN score -1.6292
CADD Raw score (version 1.3) -0.379613 (Deleterious)
FATHMM raw prediction score 0.00897 (Tolerated)
SIFT score 0.48 (Tolerated)
LRT score 0.063
MutationTaster score 1 (Tolerated)
MutatioinAssessor score 1.245 (Tolerated)
PROVEAN score -1.53 (Tolerated)
MetaSVM score -0.6 (Tolerated)
MetaLR score 0.462 (Tolerated)
MCAP score 0.055 (Deleterious)
FitCons score 0.554 (Highly Significant p < 0.003 )
Genomic Evolutionary Rate Profiling (GERP) score -2.22
PhyloP score based on multiple alignment of 100 vertebrates -1.706
PhastCons score based on multiple alignment of 100 vertebrates 0
SiPhy log transformed odds ratio on multiple alignment of 29 mammals 7.549
Deleterious probability by iFish2 0.0268 (Neutral)
Deleterious probability by DeFine 0.71 (Deleterious)
Entrez Gene ID 8529 (NCBI Gene)
Official Gene Symbol CYP4F2 (GeneCards)
Number of variants in CYP4F2 in this database 3 (view all the variants)
Full name cytochrome P450 family 4 subfamily F member 2
Band 19p13.12
Other IDs Vega: OTTHUMG00000185995
OMIM: 604426
HGNC: HGNC:2645
Ensembl: ENSG00000186115
Other names CPF2
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 protein localizes to the endoplasmic reticulum. The enzyme starts the process of inactivating and degrading leukotriene B4, a potent mediator of inflammation. This gene is part of a cluster of cytochrome P450 genes on chromosome 19. Another member of this family, CYP4F11, is approximately 16 kb away. [provided by RefSeq, Jul 2008]

Individual #1

Individual ID 29217584.04 (view all the variants in this individual)
Pubmed ID 29217584
Whose mosaic mutation Normal  
Phenotype 1  
Disease Asymptomatic
OMIM ID

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;