Overview

Variant ID 1666
Entrez Gene ID 55733
Gene HHAT (GeneCards)
Location hg19 1:210625900-210625900
hg38 1:210452556-210452556
Disease Asymptomatic
Method HiSeq X Ten
Mutation(HGVS format) NC_000001.10:g.210625900 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 249250621

Annotations and predictions

MAF in gnomAD genome (version 2.0.1) 0.00003228
EIGEN score 0.116
CADD Raw score (version 1.3) 0.135793 (Deleterious)
FATHMM raw prediction score 0.15425 (Tolerated)
Deleterious probability by DeFine 0.4267 (Neutral)
Entrez Gene ID 55733 (NCBI Gene)
Official Gene Symbol HHAT (GeneCards)
Number of variants in HHAT in this database 8 (view all the variants)
Full name hedgehog acyltransferase
Band 1q32.2
Other IDs Vega: OTTHUMG00000036447
OMIM: 605743
HGNC: HGNC:18270
Ensembl: ENSG00000054392
Other names Skn, SKI1, MART2
Summary 'Skinny hedgehog' (SKI1) encodes an enzyme that acts within the secretory pathway to catalyze amino-terminal palmitoylation of 'hedgehog' (see MIM 600725).[supplied by OMIM, Jul 2002]

Individual #1

Individual ID 29217584.03 (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;