Variant #0000313096 (NC_000012.11:g.1017197C>T, NM_018979.3:c.6828C>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.1017197C>T
DNA change (hg38) g.908031C>T
Published as WNK1(NM_001184985.2):c.7608C>T (p.Y2536=)
ISCN -
DB-ID WNK1_000005 See all 4 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) 0.997 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2018-01-15 20:58:59 +01:00 (CET)
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.6828C>T r.(?) p.(Tyr2276=)
RAD52 NM_134424.2 -/. - c.*5360G>A r.(=) p.(=)
WNK1 NM_213655.4 -/. - c.7584C>T r.(?) p.(Tyr2528=)


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