Variant #0000577012 (NC_000023.10:g.66765225_66765227del, NM_000044.3:c.237_239del (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.66765225_66765227del
DNA change (hg38) g.67545383_67545385del
Published as AR(NM_000044.4):c.237_239delGCA (p.Q80del), AR(NM_000044.6):c.237_239del (p.(Gln80del)), AR(NM_000044.6):c.237_239delGCA (p.Q80del)
ISCN -
DB-ID AR_000004 See all 25 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 2019-07-18 18:22:55 +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.237_239del - r.(?) p.(Gln80del) - -


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