Variant #0000852493 (NC_000010.10:g.50178242A>G, NM_020945.1:c.8836A>G (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.50178242A>G
DNA change (hg38) -
Published as WDFY4(NM_020945.1):c.8836A>G (p.T2946A)
ISCN -
DB-ID WDFY4_000017
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) 1.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2022-05-09 15:40:45 +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     
LRRC18 NM_001006939.3 ?/. - c.-56042T>C r.(?) p.(=)
WDFY4 NM_020945.1 ?/. - c.8836A>G r.(?) p.(Thr2946Ala)


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