Variant #0001034700 (NC_000004.11:g.85600239_85600256del, NM_014991.4:c.9965_9982del (WDFY3))

Chromosome 4
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.85600239_85600256del
DNA change (hg38) -
Published as WDFY3(NM_014991.6):c.9965_9982del (p.(Trp3322_Gly3327del))
ISCN -
DB-ID WDFY3_000063
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 2025-05-05 21:14:00 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
WDFY3 NM_014991.4 -?/. - c.9965_9982del r.(?) p.(Trp3322_Gly3327del)


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