Variant #0001006913 (NC_000023.10:g.66766412C>T, NM_000044.3:c.1424C>T (AR))

Chromosome X
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.66766412C>T
DNA change (hg38) -
Published as AR(NM_000044.3):c.1424C>T (p.(Ala475Val)), AR(NM_000044.4):c.1424C>T (p.A475V), AR(NM_000044.6):c.1424C>T (p.A475V)
ISCN -
DB-ID AR_000321 See all 8 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) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited 2025-05-05 21:14:00 +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.1424C>T - r.(?) p.(Ala475Val) - -


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