Variant #0008892822 (NC_000014.8:g.74766999A>G, NC_000014.8(NM_005050.3):c.39-28T>C (ABCD4))
Chromosome |
14 |
Affects function (as reported) |
Not classified |
Affects function (by curator) |
Not classified |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.74766999A>G |
DB-ID |
- |
dbSNP ID |
rs751756131 |
gnomAD frequency |
4/244816 |
gnomAD homozygote count |
0/122404 |
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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