Variant #0001948296 (NC_000023.10:g.205365_205367del, NC_000023.10(NM_018390.3):c.128-35_128-33del (PLCXD1))

Chromosome X
DNA change (genomic) (Relative to hg19 / GRCh37) g.205365_205367del
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID PLCXD1_000019
Frequency 3/12504
Freq. EA 0/8246
Freq. AA 3/4258
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 2014-05-04 14:55:28 +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.128-35_128-33del r.(=) p.(=)