Variant #0009677627 (NC_000016.9:g.8839882C>T, NM_000663.4:c.95C>T (ABAT))
Chromosome |
16 |
Affects function (as reported) |
Not classified |
Affects function (by curator) |
Not classified |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.8839882C>T |
DB-ID |
- |
dbSNP ID |
rs758948605 |
gnomAD frequency |
2/246112 |
gnomAD homozygote count |
0/123054 |
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
|
|