Variant #0000849983 (NC_000002.11:g.63720067T>A, NM_015910.5:c.83A>T (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.63720067T>A
DNA change (hg38) -
Published as WDPCP(NM_015910.6):c.83A>T (p.D28V), WDPCP(NM_015910.7):c.83A>T (p.D28V)
ISCN -
DB-ID WDPCP_000025 See all 3 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) 0.00158 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
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     
WDPCP NM_015910.5 -?/. - c.83A>T r.(?) p.(Asp28Val)


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