Variant #0000321512 (NC_000010.10:g.50015901T>C, NC_000010.10(NM_020945.1):c.4739-3T>C (WDFY4))

Chromosome 10
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.50015901T>C
DNA change (hg38) g.48807856T>C
Published as WDFY4(NM_020945.1):c.4739-3T>C (p.?)
ISCN -
DB-ID WDFY4_000005
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) 0.00067 View details
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 2020-06-26 14:29:30 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LRRC18 NM_001006939.3 ?/. - c.*102381A>G r.(=) p.(=)
WDFY4 NM_020945.1 ?/. - c.4739-3T>C r.spl? p.?


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