Variant #0000311376 (NC_000012.11:g.1020266T>C, NM_018979.3:c.*2308T>C (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.1020266T>C
DNA change (hg38) g.911100T>C
Published as WNK1(NM_001184985.2):c.*2308T>C
ISCN -
DB-ID WNK1_000055
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.*2308T>C r.(=) p.(=)
RAD52 NM_134424.2 -/. - c.*2291A>G r.(=) p.(=)
WNK1 NM_213655.4 -/. - c.*2308T>C r.(=) p.(=)


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