Variant #0008892832 (NC_000014.8:g.74769557C>T, NC_000014.8(NM_005050.3):c.38+21G>A (ABCD4))
Chromosome |
14 |
Affects function (as reported) |
Not classified |
Affects function (by curator) |
Not classified |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.74769557C>T |
DB-ID |
- |
dbSNP ID |
rs574228631 |
gnomAD frequency |
35/231934 |
gnomAD homozygote count |
1/115933 |
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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