Variant #0008891906 (NC_000014.8:g.74753568G>A, NM_005050.3:c.1637-49delCinsT (ABCD4))
| Chromosome |
14 |
| Affects function (as reported) |
Not classified |
| Affects function (by curator) |
Not classified |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.74753568G>A |
| DB-ID |
- |
| dbSNP ID |
rs745991739 |
| gnomAD frequency |
4/219588 |
| gnomAD homozygote count |
0/109789 |
| 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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