Variant #0013079682 (NC_000023.10:g.152989046G>A, NC_000023.10(NM_001256447.1):c.-44-303C>T (BCAP31))
Chromosome |
X |
Affects function (as reported) |
Not classified |
Affects function (by curator) |
Not classified |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.152989046G>A |
DB-ID |
- |
dbSNP ID |
rs781974660 |
gnomAD frequency |
2/108782 |
gnomAD homozygote count |
0/74242 |
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
|
|