Variant #0000262777 (NC_000023.10:g.66931295C>A, NM_000044.3:c.1937C>A (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.66931295C>A
DNA change (hg38) g.67711453C>A
Published as AR(NM_000044.3):c.1937C>A (p.(Ala646Asp)), AR(NM_000044.6):c.1937C>A (p.A646D), AR(NM_001011645.3):c.341C>A (p.A114D)
ISCN -
DB-ID AR_000006 See all 13 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) 0.00113 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2024-08-28 13:16:32 +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.1937C>A - r.(?) p.(Ala646Asp) - -


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