Variant #0000913729 (NC_000012.11:g.1017830G>A, NM_018979.3:c.7021G>A (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.1017830G>A
DNA change (hg38) -
Published as WNK1(NM_001184985.1):c.7801G>A (p.G2601S)
ISCN -
DB-ID RAD52_000006
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) 0.00045 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 2023-01-11 15:44:22 +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.7021G>A r.(?) p.(Gly2341Ser)
RAD52 NM_134424.2 -?/. - c.*4727C>T r.(=) p.(=)
WNK1 NM_213655.4 -?/. - c.7777G>A r.(?) p.(Gly2593Ser)


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