Variant #0000247129 (NC_000012.11:g.970306del, NM_018979.3:c.1748del (WNK1))

Chromosome 12
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.970306del
DNA change (hg38) g.861140del
Published as WNK1(NM_001184985.2):c.1748delA (p.K583Sfs*11)
ISCN -
DB-ID WNK1_000066
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_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
WNK1 NM_018979.3 -/. - c.1748del r.(?) p.(Lys583SerfsTer11)
WNK1 NM_213655.4 -/. - c.1748del r.(?) p.(Lys583SerfsTer11)


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