Variant #0007859631 (NC_000012.11:g.22089451_22089452insT, NC_000012.11(NM_005691.2):c.142+15dupA (ABCC9))
Chromosome |
12 |
Affects function (as reported) |
Not classified |
Affects function (by curator) |
Not classified |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.22089451_22089452insT |
DB-ID |
- |
dbSNP ID |
rs571187142 |
gnomAD frequency |
225/243216 |
gnomAD homozygote count |
1/121384 |
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
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