Variant #0005363082 (NC_000007.13:g.150922107_150922108insTC, NC_000007.13(NM_007189.2):c.155-34_155-33insGA (ABCF2))
| Chromosome |
7 |
| Affects function (as reported) |
Not classified |
| Affects function (by curator) |
Not classified |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.150922107_150922108insTC |
| DB-ID |
- |
| dbSNP ID |
rs750381837 |
| gnomAD frequency |
6/243316 |
| gnomAD homozygote count |
0/121652 |
| 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
|
|