Variant #0000311330 (NC_000002.11:g.63720034G>T, NM_015910.5:c.116C>A (WDPCP))

Chromosome 2
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.63720034G>T
DNA change (hg38) g.63492900G>T
Published as WDPCP(NM_001354044.1):c.44C>A (p.T15N), WDPCP(NM_015910.7):c.116C>A (p.T39N)
ISCN -
DB-ID WDPCP_000024 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) Retrieve
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2018-01-15 20:58:59 +01:00 (CET)
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     
WDPCP NM_015910.5 -/. - c.116C>A r.(?) p.(Thr39Asn)


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