Variant #0001948280 (NC_000023.10:g.200860T>C, NM_018390.3:c.6T>C (PLCXD1))

Chromosome X
DNA change (genomic) (Relative to hg19 / GRCh37) g.200860T>C
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID PLCXD1_000003
Frequency 10384/12998
Freq. EA 6348/8592
Freq. AA 4036/4406
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 2014-06-07 18:20:23 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
PLCXD1 NM_018390.3 ?/? c.6T>C r.(=) p.(=)