Variant #0000329544 (NC_000003.11:g.113003372_113003385del, NM_001164496.1:c.*7022_*7035del (WDR52))

Chromosome 3
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.113003372_113003385del
DNA change (hg38) g.113284525_113284538del
Published as BOC(NM_001378074.1):c.2847_2860del (p.(Gly950Alafs*12))
ISCN -
DB-ID BOC_000001
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 2018-01-15 20:58:59 +01:00 (CET)
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)     

RNA change     

Protein     
WDR52 NM_001164496.1 ?/. - c.*7022_*7035del r.(=) p.(=)
BOC NM_033254.2 ?/. - c.2844_2857del r.(?) p.(Gly949AlafsTer12)


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