Variant #0001031066 (NC_000001.10:g.113051966G>A, NM_024494.2:c.82G>A (WNT2B))

Chromosome 1
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.113051966G>A
DNA change (hg38) -
Published as WNT2B(NM_024494.3):c.82G>A (p.A28T, p.(Ala28Thr))
ISCN -
DB-ID WNT2B_000002 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) 0.00114 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 2025-05-05 21:14:00 +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     
WNT2B NM_004185.3 -?/. - c.126-5530G>A r.(=) p.(=)
WNT2B NM_024494.2 -?/. - c.82G>A r.(?) p.(Ala28Thr)


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