Variant #0000608212 (NC_000003.11:g.113025123G>A, NM_001164496.1:c.4683C>T (WDR52))

Chromosome 3
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.113025123G>A
DNA change (hg38) g.113306276G>A
Published as CFAP44(NM_001164496.2):c.4683C>T (p.D1561=)
ISCN -
DB-ID BOC_000004
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 2019-12-04 14:54:23 +01:00 (CET)
Date last edited 2020-06-15 12:36:43 +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.4683C>T r.(?) p.(Asp1561=)
BOC NM_033254.2 -?/. - c.*19414G>A r.(=) p.(=)


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