Variant #0009677609 (NC_000016.9:g.8839811G>T, NC_000016.9(NM_000663.4):c.71-47G>T (ABAT))
Chromosome |
16 |
Affects function (as reported) |
Not classified |
Affects function (by curator) |
Not classified |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.8839811G>T |
DB-ID |
- |
dbSNP ID |
- |
gnomAD frequency |
1/243868 |
gnomAD homozygote count |
0/121933 |
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
|
|