Variant #0000250802 (NC_000002.11:g.63714613A>T, NM_015910.5:c.176T>A (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.63714613A>T
DNA change (hg38) g.63487479A>T
Published as WDPCP(NM_015910.6):c.176T>A (p.I59N), WDPCP(NM_015910.7):c.176T>A (p.I59N)
ISCN -
DB-ID WDPCP_000020 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) 0.00131 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
WDPCP NM_015910.5 -?/. - c.176T>A r.(?) p.(Ile59Asn)


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