Overview

Variant ID 26581
Entrez Gene ID 2131
Gene EXT1 (GeneCards)
Location hg19 8:119134332-119134332
hg38 8:118122093-118122093
Disease Asymptomatic
Method Single cell Sequencing Cell cloning
Mutation(HGVS format) NC_000008.10:g.119134332 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 146364022

Annotations and predictions

MAF in gnomAD genome (version 2.0.1) 0
EIGEN score -0.1762
CADD Raw score (version 1.3) -0.338409 (Deleterious)
FATHMM raw prediction score 0.12782 (Tolerated)
Deleterious probability by DeFine 0.6514 (Deleterious)
Entrez Gene ID 2131 (NCBI Gene)
Official Gene Symbol EXT1 (GeneCards)
Number of variants in EXT1 in this database 6 (view all the variants)
Full name exostosin glycosyltransferase 1
Band 8q24.11
Other IDs Vega: OTTHUMG00000059718
OMIM: 608177
HGNC: HGNC:3512
Ensembl: ENSG00000182197
Other names EXT, LGS, TTV, LGCR, TRPS2
Summary This gene encodes an endoplasmic reticulum-resident type II transmembrane glycosyltransferase involved in the chain elongation step of heparan sulfate biosynthesis. Mutations in this gene cause the type I form of multiple exostoses. [provided by RefSeq, Jul 2008]

Individual #1

Individual ID 29217587.02 (view all the variants in this individual)
Pubmed ID 29217587
Whose mosaic mutation Normal  
Phenotype 1  
Disease Asymptomatic
OMIM ID