Variant #0000577037 (NC_000023.10:g.66941751C>G, NM_000044.3:c.2395C>G (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.66941751C>G
DNA change (hg38) g.67721909C>G
Published as AR(NM_000044.3):c.2395C>G (p.(Gln799Glu)), AR(NM_000044.4):c.2395C>G (p.Q799E), AR(NM_000044.6):c.2395C>G (p.Q799E), AR(NM_001011645.3):c.799C>G ...)
ISCN -
DB-ID AR_000019 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) 0.00143 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
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.2395C>G - r.(?) p.(Gln799Glu) - -


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