Variant #0012817364 (NC_000023.10:g.200816C>T, NC_000023.10(NM_018390.3):c.-21-18C>T (PLCXD1))

Chromosome X
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.200816C>T
DB-ID -
dbSNP ID rs367885899
gnomAD frequency 1/244874
gnomAD homozygote count 0/122436
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.-21-18C>T r.(=) p.(=)