Variant #0000619777 (NC_000023.10:g.66765219_66765227dup, NM_000044.3:c.231_239dup (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.66765219_66765227dup
DNA change (hg38) g.67545377_67545385dup
Published as AR(NM_000044.3):c.171_179dup (p.(Gln60_Gln61insGlnGlnGln)), AR(NM_000044.4):c.231_239dupGCAGCAGCA (p.Q78_Q80dup), AR(NM_000044.6):c.231_239dupGCAGC...
ISCN -
DB-ID AR_000622 See all 12 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 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2024-02-26 20:06:56 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Haplotype     

RNA change     

Protein     

P-domain     

Enzyme activity     
AR NM_000044.3 -?/. - c.231_239dup - r.(?) p.(Gln78_Gln80dup) - -


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.