Variant #0009873397 (NC_000016.9:g.48278373C>T, NM_031490.2:c.74C>T (LONP2))
Chromosome |
16 |
Affects function (as reported) |
Not classified |
Affects function (by curator) |
Not classified |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.48278373C>T |
DB-ID |
- |
dbSNP ID |
rs764266328 |
gnomAD frequency |
2/226952 |
gnomAD homozygote count |
0/113474 |
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 |
Variant on transcripts
|
|