Variant #0008574281 (NC_000013.10:g.95953546_95953547insCCT, NM_005845.3:c.22_23insAGG (ABCC4))
Chromosome |
13 |
Affects function (as reported) |
Not classified |
Affects function (by curator) |
Not classified |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.95953546_95953547insCCT |
DB-ID |
- |
dbSNP ID |
- |
gnomAD frequency |
1/221546 |
gnomAD homozygote count |
0/110771 |
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
|
|