Variant #0000856734 (NC_000023.10:g.66766162C>T, NM_000044.3:c.1174C>T (AR))

Chromosome X
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.66766162C>T
DNA change (hg38) -
Published as AR(NM_000044.3):c.1174C>T (p.(Pro392Ser)), AR(NM_000044.4):c.1174C>T (p.P392S), AR(NM_000044.6):c.1174C>T (p.P392S)
ISCN -
DB-ID AR_000218 See all 15 reported entries
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00454 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2022-05-09 15:47:41 +02:00 (CEST)
Date last edited N/A
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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.1174C>T - r.(?) p.(Pro392Ser) - -


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