Variant #0000608211 (NC_000003.11:g.113005589T>A, NM_001164496.1:c.*4815A>T (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.113005589T>A
DNA change (hg38) g.113286742T>A
Published as BOC(NM_033254.3):c.3225T>A (p.S1075R)
ISCN -
DB-ID BOC_000003
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) 0.0002 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-12-04 14:54:23 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
WDR52 NM_001164496.1 ?/. - c.*4815A>T r.(=) p.(=)
BOC NM_033254.2 ?/. - c.3225T>A r.(?) p.(Ser1075Arg)


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