Variant #0000321509 (NC_000010.10:g.49931602T>C, NM_020945.1:c.581T>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.49931602T>C
DNA change (hg38) g.48723557T>C
Published as WDFY4(NM_020945.1):c.581T>C (p.(Met194Thr))
ISCN -
DB-ID WDFY4_000002
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) 2.0E-5 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 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LRRC18 NM_001006939.3 ?/. - c.*186680A>G r.(=) p.(=)
WDFY4 NM_020945.1 ?/. - c.581T>C r.(?) p.(Met194Thr)


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