Overview

Variant ID 31368
Entrez Gene ID 9817
Gene KEAP1 (GeneCards)
Location hg19 19:10610687-10610687
hg38 19:10500011-10500011
Disease Asymptomatic
Method NGS gene panel
Mutation(HGVS format) NC_000019.9:g.10610687 C>T (Genome Assembly: hg19)

Other information

Exon or Intron Exon
Position in protein 8
Amino acid changes in protein S > N
Position in cDNA 23
Changes in cDNA G > A
mRNA accession NA
mRNA length NA
Reference length 59128983

Annotations and predictions

MAF in gnomAD genome (version 2.0.1) 0
EIGEN score 0.0513
CADD Raw score (version 1.3) 3.490641 (Deleterious)
FATHMM raw prediction score 0.85708 (Tolerated)
SIFT score 0 (Deleterious)
LRT score 0 (Deleterious)
MutationTaster score 0.934 (Tolerated)
MutatioinAssessor score 0 (Tolerated)
PROVEAN score -0.54 (Tolerated)
MetaSVM score -0.91 (Tolerated)
MetaLR score 0.18 (Tolerated)
MCAP score 0.026 (Deleterious)
FitCons score 0.731 (Highly Significant p < 0.003 )
Genomic Evolutionary Rate Profiling (GERP) score 3.89
PhyloP score based on multiple alignment of 100 vertebrates 0.563
PhastCons score based on multiple alignment of 100 vertebrates 0.013
SiPhy log transformed odds ratio on multiple alignment of 29 mammals 9.833
Deleterious probability by iFish2 0.2057 (Neutral)
Deleterious probability by DeFine 0.8991 (Deleterious)
Entrez Gene ID 9817 (NCBI Gene)
Official Gene Symbol KEAP1 (GeneCards)
Number of variants in KEAP1 in this database 11 (view all the variants)
Full name kelch like ECH associated protein 1
Band 19p13.2
Other IDs Vega: OTTHUMG00000180579
OMIM: 606016
HGNC: HGNC:23177
Ensembl: ENSG00000079999
Other names INrf2, KLHL19
Summary This gene encodes a protein containing KELCH-1 like domains, as well as a BTB/POZ domain. Kelch-like ECH-associated protein 1 interacts with NF-E2-related factor 2 in a redox-sensitive manner and the dissociation of the proteins in the cytoplasm is followed by transportation of NF-E2-related factor 2 to the nucleus. This interaction results in the expression of the catalytic subunit of gamma-glutamylcysteine synthetase. Two alternatively spliced transcript variants encoding the same isoform have been found for this gene. [provided by RefSeq, Jul 2008]

Individual #1

Individual ID 25999502.02 (view all the variants in this individual)
Pubmed ID 25999502
Whose mosaic mutation Normal  
Origin of mosaic mutation in patients de novo
Phenotype 1  
Disease Asymptomatic
OMIM ID

Publication #1: 25999502

Pubmed ID 25999502
Title High burden and pervasive positive selection of somatic mutations in normal human skin
Journal Science
Publication date 2015.05
Disease Asymptomatic
Number of cases Male cases: 1; Female cases: 3;