Variant #0000853537 (NC_000012.11:g.863415C>T, NM_018979.3:c.684C>T (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.863415C>T
DNA change (hg38) -
Published as WNK1(NM_001184985.1):c.684C>T (p.G228=), WNK1(NM_001184985.2):c.684C>T (p.G228=)
ISCN -
DB-ID WNK1_000077 See all 2 reported entries
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) 0.00274 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 2022-05-09 15:40:45 +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.684C>T r.(?) p.(Gly228=)
WNK1 NM_213655.4 -/. - c.684C>T r.(?) p.(Gly228=)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.