Variant #0000877057 (NC_000023.10:g.66905906G>A, NM_000044.3:c.1823G>A (AR))

Chromosome X
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.66905906G>A
DNA change (hg38) -
Published as -
ISCN -
DB-ID AR_000011 See all 9 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs137852573
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2022-08-23 11:06:01 +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)     

Haplotype     

RNA change     

Protein     

P-domain     

Enzyme activity     
AR NM_000044.3 +/. - c.1823G>A - r.(?) p.(Arg608Gln) - -


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