Variant #0001236351 (NC_000001.10:g.229693952C>A, NM_012089.2:c.448G>T (ABCB10))
Chromosome |
1 |
Affects function (as reported) |
Not classified |
Affects function (by curator) |
Not classified |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.229693952C>A |
DB-ID |
- |
dbSNP ID |
rs4148756 |
gnomAD frequency |
713/52900 |
gnomAD homozygote count |
26/25761 |
Average frequency (gnomAD v.2.1.1) |
0.01348 View details |
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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