Variant #0001681333 (NC_000019.9:g.282266C>T, NM_003712.2:c.585G>A (PPAP2C))

Chromosome 19
DNA change (genomic) (Relative to hg19 / GRCh37) g.282266C>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID PPAP2C_000017
Frequency 2/13006
Freq. EA 2/8600
Freq. AA 0/4406
Average frequency (gnomAD v.2.1.1) -
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Ivo F.A.C. Fokkema
Date created 2013-05-03 16:45:39 +02:00 (CEST)
Date last edited 2014-05-02 14:20:55 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
PPAP2C NM_003712.2 ?/? c.585G>A r.(=) p.(=)