Variant #0013079630 (NC_000023.10:g.152988611T>C, NM_001256447.1:c.89A>G (BCAP31))
Chromosome |
X |
Affects function (as reported) |
Not classified |
Affects function (by curator) |
Not classified |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.152988611T>C |
DB-ID |
- |
dbSNP ID |
rs144781058 |
gnomAD frequency |
2/177525 |
gnomAD homozygote count |
0/121910 |
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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