Overview

Variant ID 2961
Entrez Gene ID 2492
Gene FSHR (GeneCards)
Location hg19 2:49561529-49561529
hg38 2:49334390-49334390
Disease Asymptomatic
Method HiSeq X Ten
Mutation(HGVS format) NC_000002.11:g.49561529 A>C (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
EIGEN score -0.1426
CADD Raw score (version 1.3) -0.135042 (Deleterious)
FATHMM raw prediction score 0.11619 (Tolerated)
Deleterious probability by DeFine 0.5396 (Deleterious)
Entrez Gene ID 2492 (NCBI Gene)
Official Gene Symbol FSHR (GeneCards)
Number of variants in FSHR in this database 11 (view all the variants)
Full name follicle stimulating hormone receptor
Band 2p16.3
Other IDs Vega: OTTHUMG00000129259
OMIM: 136435
HGNC: HGNC:3969
Ensembl: ENSG00000170820
Other names LGR1, ODG1, FSHR1, FSHRO
Summary The protein encoded by this gene belongs to family 1 of G-protein coupled receptors. It is the receptor for follicle stimulating hormone and functions in gonad development. Mutations in this gene cause ovarian dysgenesis type 1, and also ovarian hyperstimulation syndrome. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2010]

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;