Variant #0000807970 (NC_000017.10:g.40946970C>A, NM_032387.4:c.2531C>A (WNK4))

Chromosome 17
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.40946970C>A
DNA change (hg38) -
Published as WNK4(NM_032387.5):c.2531C>A (p.S844Y)
ISCN -
DB-ID BECN1_000003
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2021-09-17 14:40:49 +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     
BECN1 NM_003766.3 ?/. - c.*15808G>T r.(=) p.(=)
WNK4 NM_032387.4 ?/. - c.2531C>A r.(?) p.(Ser844Tyr)
CNTD1 NM_173478.2 ?/. - c.-4116C>A r.(?) p.(=)


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