Variant #0000814351 (NC_000009.11:g.127265389C>G, NM_004959.4:c.213G>C (NR5A1))

Chromosome 9
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.127265389C>G
DNA change (hg38) -
Published as -
ISCN -
DB-ID NR5A1_000113
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs865902758
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2021-10-12 10:25:02 +02:00 (CEST)
Date last edited 2022-09-26 12:22:42 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NR5A1 NM_004959.4 +?/. - c.213G>C r.(?) p.(Gln71His)


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