Variant #0000001471 (NC_000002.11:g.49210264G>A, NM_000145.3:c.566C>T (FSHR))

Chromosome 2
Allele Both (homozygous)
Affects function (as reported) Affects function
Affects function (by curator) Affects function
Classification method -
Clinical classification pathogenic (recessive)
DNA change (genomic) (Relative to hg19 / GRCh37) g.49210264G>A
DNA change (hg38) g.48983125G>A
Published as -
ISCN -
DB-ID FSHR_000002 See all 17 reported entries
Variant remarks in vitro functional analysis shows dramatic reduction of binding capacity and signal transduction of the variant receptor
Reference PubMed: Aittomaki 1995, OMIM:var0001
ClinVar ID -
dbSNP ID rs121909658
Origin SUMMARY record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00076 View details
Owner Anne Polvi
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Anne Polvi
Date created 2012-08-23 16:32:11 +02:00 (CEST)
Date last edited 2023-02-08 13:39:32 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FSHR NM_000145.3 +/+ 7 c.566C>T r.(566c>u) p.(Ala189Val)


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