Variant #0012817422 (NC_000023.10:g.200961T>G, NM_018390.3:c.107T>G (PLCXD1))

Chromosome X
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.200961T>G
DB-ID -
dbSNP ID rs369464388
gnomAD frequency 1/245538
gnomAD homozygote count 0/122768
Average frequency (gnomAD v.2.1.1) Retrieve
Database submission license No license selected
Created by LOVD
Date created 2017-02-27 00:00:00 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
PLCXD1 NM_018390.3 ./. c.107T>G r.(?) p.(Leu36Arg)