Variant #0004852277 (NC_000007.13:g.20778662C>T, NM_001163941.1:c.2924delCinsT (ABCB5))
Chromosome |
7 |
Affects function (as reported) |
Not classified |
Affects function (by curator) |
Not classified |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.20778662C>T |
DB-ID |
- |
dbSNP ID |
rs764899745 |
gnomAD frequency |
0/243776 |
gnomAD homozygote count |
0/121887 |
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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