Variant #0001948331 (NC_000023.10:g.207471T>G, NC_000023.10(NM_018390.3):c.393+28T>G (PLCXD1))

Chromosome X
DNA change (genomic) (Relative to hg19 / GRCh37) g.207471T>G
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID PLCXD1_000054
Frequency 233/12998
Freq. EA 1/8592
Freq. AA 232/4406
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 2014-05-15 20:45:39 +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.393+28T>G r.(=) p.(=)