Variant #0000577005 (NC_000023.10:g.66765219_66765227del, NM_000044.3:c.231_239del (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.66765219_66765227del
DNA change (hg38) g.67545377_67545385del
Published as AR(NM_000044.4):c.231_239delGCAGCAGCA (p.Q78_Q80del), AR(NM_000044.6):c.231_239delGCAGCAGCA (p.Q78_Q80del)
ISCN -
DB-ID AR_000581 See all 23 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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
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.231_239del - r.(?) p.(Gln78_Gln80del) - -


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