Variant #0000890844 (NC_000012.11:g.987416A>C, NM_018979.3:c.2262A>C (WNK1))

Chromosome 12
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.987416A>C
DNA change (hg38) -
Published as WNK1(NM_001184985.1):c.3501A>C (p.T1167=)
ISCN -
DB-ID WNK1_000133
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_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2022-11-01 13:01:21 +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     
WNK1 NM_018979.3 -?/. - c.2262A>C r.(?) p.(Thr754=)
WNK1 NM_213655.4 -?/. - c.3756A>C r.(?) p.(Thr1252=)


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