Overview

Variant ID 24938
Entrez Gene ID 3667
Gene IRS1 (GeneCards)
Location hg19 2:227668049-227668049
hg38 2:226803333-226803333
Disease Asymptomatic
Method Single cell Sequencing Cell cloning
Mutation(HGVS format) NC_000002.11:g.227668049 T>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 243199373

Annotations and predictions

MAF in gnomAD genome (version 2.0.1) 0.0909
SNP ID (dbSNP ID version 137) rs62190996
EIGEN score -0.64
CADD Raw score (version 1.3) -0.457062 (Deleterious)
FATHMM raw prediction score 0.09104 (Tolerated)
Deleterious probability by DeFine 0.0557 (Neutral)
Entrez Gene ID 3667 (NCBI Gene)
Official Gene Symbol IRS1 (GeneCards)
Number of variants in IRS1 in this database 3 (view all the variants)
Full name insulin receptor substrate 1
Band 2q36.3
Other IDs Vega: OTTHUMG00000133179
OMIM: 147545
HGNC: HGNC:6125
Ensembl: ENSG00000169047
Other names HIRS-1
Summary This gene encodes a protein which is phosphorylated by insulin receptor tyrosine kinase. Mutations in this gene are associated with type II diabetes and susceptibility to insulin resistance. [provided by RefSeq, Nov 2009]

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