Variant #0001050672 (NC_000002.11:g.63587053A>G, NC_000002.11(NM_015910.5):c.1748+18468T>C (WDPCP))

Chromosome 2
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.63587053A>G
DNA change (hg38) -
Published as WDPCP(NM_001354045.2):c.1907T>C (p.(Phe636Ser))
ISCN -
DB-ID WDPCP_000066
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-11-01 13:22:20 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
WDPCP NM_015910.5 -?/. - c.1748+18468T>C r.(=) p.(=)


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