Variant #0000623003 (NC_000012.11:g.977296T>C, NC_000012.11(NM_018979.3):c.2140-3135T>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.977296T>C
DNA change (hg38) g.868130T>C
Published as WNK1(NM_001184985.2):c.2404T>C (p.L802=)
ISCN -
DB-ID WNK1_000109
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) 0.00035 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 2019-12-06 12:43:26 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
WNK1 NM_018979.3 -?/. - c.2140-3135T>C r.(=) p.(=)
WNK1 NM_213655.4 -?/. - c.2659T>C r.(?) p.(Leu887=)


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