Variant #0000853230 (NC_000012.11:g.1023218G>T, NM_018979.3:c.*5260G>T (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.1023218G>T
DNA change (hg38) -
Published as RAD52(NM_134424.2):c.1037C>A (p.(Ser346*))
ISCN -
DB-ID RAD52_000005
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) 0.01651 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 2022-05-09 15:40:45 +02:00 (CEST)
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.*5260G>T r.(=) p.(=)
RAD52 NM_134424.2 -?/. - c.1037C>A r.(?) p.(Ser346*)
WNK1 NM_213655.4 -?/. - c.*5260G>T r.(=) p.(=)


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