Variant #0000334273 (NC_000023.10:g.54359884A>C, NM_020922.4:c.223T>G (WNK3))

Chromosome X
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.54359884A>C
DNA change (hg38) g.54333451A>C
Published as WNK3(NM_001002838.3):c.223T>G (p.(Ser75Ala)), WNK3(NM_020922.4):c.223T>G (p.S75A)
ISCN -
DB-ID WNK3_000033 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) 0.00046 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2019-12-04 15:24:38 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
WNK3 NM_020922.4 ?/. - c.223T>G r.(?) p.(Ser75Ala)


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