Variant #0004955576 (NC_000007.13:g.48211138C>T, NM_152701.3:c.58C>T (ABCA13))
| Chromosome |
7 |
| Affects function (as reported) |
Not classified |
| Affects function (by curator) |
Not classified |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.48211138C>T |
| DB-ID |
- |
| dbSNP ID |
- |
| gnomAD frequency |
1/137360 |
| gnomAD homozygote count |
0/68679 |
| 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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