Variant #0000718918 (NC_000002.11:g.63631343A>C, NM_015910.5:c.1275T>G (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.63631343A>C
DNA change (hg38) -
Published as WDPCP(NM_001354044.1):c.1203T>G (p.T401=), WDPCP(NM_015910.7):c.1275T>G (p.T425=)
ISCN -
DB-ID WDPCP_000009 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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-02-08 18:36:18 +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.1275T>G r.(?) p.(Thr425=)


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