Variant #0005857566 (NC_000009.11:g.14886C>T)

Chromosome 9
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.14886C>T
DB-ID -
dbSNP ID rs566352560
gnomAD frequency 8/179518
gnomAD homozygote count 0/89751
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
Options




Variant on transcripts

Stop! No variants on transcripts found!

  Powered by LOVD v.3.0 Build 30
LOVD software ©2004-2024 Leiden University Medical Center 		Checking for LOVD updates...