Variant #0012461398 (NC_000021.8:g.43640127_43640128insCGG, NC_000021.8(NM_207628.1):c.-24-5654_-24-5653insCGG (ABCG1))
Chromosome |
21 |
Affects function (as reported) |
Not classified |
Affects function (by curator) |
Not classified |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.43640127_43640128insCGG |
DB-ID |
- |
dbSNP ID |
rs768217098 |
gnomAD frequency |
10/151568 |
gnomAD homozygote count |
0/75774 |
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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