Variant #0012203097 (NC_000020.10:g.34832597T>G, NM_001271874.1:c.758-22delTinsG (AAR2))
Chromosome |
20 |
Affects function (as reported) |
Not classified |
Affects function (by curator) |
Not classified |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.34832597T>G |
DB-ID |
- |
dbSNP ID |
rs771074176 |
gnomAD frequency |
1/235824 |
gnomAD homozygote count |
0/117909 |
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
|
|