Variant #0000549560 (NC_000012.11:g.974311dup, NC_000012.11(NM_018979.3):c.2139+2875dup (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.974311dup
DNA change (hg38) g.865145dup
Published as WNK1(NM_213655.4):c.2175dupC (p.I726Hfs*45), WNK1(NM_213655.5):c.2175dupC (p.I726Hfs*45)
ISCN -
DB-ID WNK1_000028 See all 3 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) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
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.2139+2875dup r.(=) p.(=)
WNK1 NM_213655.4 -/. - c.2175dup r.(?) p.(Ile726HisfsTer45)


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