Variant #0001948345 (NC_000023.10:g.208276C>T, NM_018390.3:c.504C>T (PLCXD1))

Chromosome X
DNA change (genomic) (Relative to hg19 / GRCh37) g.208276C>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID PLCXD1_000068
Frequency 4/12998
Freq. EA 4/8592
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 16:50:35 +02:00 (CEST)
Date last edited 2014-04-28 05:25:40 +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.504C>T r.(=) p.(=)