Variant #0009515936 (NC_000016.9:g.64473C>T)

Chromosome 16
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.64473C>T
DB-ID -
dbSNP ID rs565431032
gnomAD frequency 99/106828
gnomAD homozygote count 35/53350
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!