Variant #0001948374 (NC_000023.10:g.209797G>A, NM_018390.3:c.645G>A (PLCXD1))

Chromosome X
DNA change (genomic) (Relative to hg19 / GRCh37) g.209797G>A
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID PLCXD1_000097
Frequency 12/12998
Freq. EA 0/8592
Freq. AA 12/4406
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 16:50:35 +02:00 (CEST)
Date last edited 2014-04-28 05:41:42 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
PLCXD1 NM_018390.3 ?/? c.645G>A r.(?) p.(Trp215*)