Variant #0000577011 (NC_000023.10:g.66765222_66765227dup, NM_000044.3:c.234_239dup (AR))

Chromosome X
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.66765222_66765227dup
DNA change (hg38) g.67545380_67545385dup
Published as AR(NM_000044.3):c.173_174insGCAGCA (p.(Gln58_Gln59insGlnGln)), AR(NM_000044.4):c.234_239dupGCAGCA (p.Q79_Q80dup), AR(NM_000044.6):c.234_239dupGCAGC...
ISCN -
DB-ID AR_000619 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) Retrieve
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2024-02-26 20:06:56 +01:00 (CET)
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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.234_239dup - r.(?) p.(Gln79_Gln80dup) - -


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