Variant #0000863156 (NC_000012.11:g.922913T>C, NM_018979.3:c.865T>C (WNK1))

Chromosome 12
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.922913T>C
DNA change (hg38) -
Published as WNK1(NM_001184985.2):c.865T>C (p.S289P)
ISCN -
DB-ID WNK1_000125
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) 0.00011 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2022-05-09 15:51:19 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
WNK1 NM_018979.3 ?/. - c.865T>C r.(?) p.(Ser289Pro)
WNK1 NM_213655.4 ?/. - c.865T>C r.(?) p.(Ser289Pro)


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