Variant #0000914822 (NC_000017.10:g.40948121T>C, NC_000017.10(NM_032387.4):c.3432-20T>C (WNK4))

Chromosome 17
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.40948121T>C
DNA change (hg38) -
Published as WNK4(NM_032387.5):c.3432-20T>C
ISCN -
DB-ID BECN1_000007
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) 0.00215 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2023-01-11 15:44:22 +01:00 (CET)
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.*14657A>G r.(=) p.(=)
WNK4 NM_032387.4 -?/. - c.3432-20T>C r.(=) p.(=)
CNTD1 NM_173478.2 -?/. - c.-2965T>C r.(?) p.(=)


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