Variant #0000539958 (NC_000010.10:g.50018610A>C, NM_020945.1:c.4874A>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.50018610A>C
DNA change (hg38) g.48810565A>C
Published as WDFY4(NM_020945.1):c.4874A>C (p.D1625A)
ISCN -
DB-ID WDFY4_000008
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 2019-07-18 18:22:55 +02:00 (CEST)
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.*99672T>G r.(=) p.(=)
WDFY4 NM_020945.1 ?/. - c.4874A>C r.(?) p.(Asp1625Ala)


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