Variant #0007642962 (NC_000011.9:g.119029687C>T, NM_001142505.1:c.1437+48delCinsT (ABCG4))
| Chromosome |
11 |
| Affects function (as reported) |
Not classified |
| Affects function (by curator) |
Not classified |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.119029687C>T |
| DB-ID |
- |
| dbSNP ID |
rs781323607 |
| gnomAD frequency |
1/244444 |
| gnomAD homozygote count |
0/122220 |
| 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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