Variant #0000311179 (NC_000001.10:g.33790449C>T, NM_198040.2:c.*17G>A (PHC2))
| Chromosome |
1 |
| Affects function (as reported) |
Not classified |
| Affects function (by curator) |
Not classified |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.33790449C>T |
| DB-ID |
- |
| dbSNP ID |
rs141285527 |
| gnomAD frequency |
164/241110 |
| gnomAD homozygote count |
1/120392 |
| Average frequency (gnomAD v.2.1.1) |
0.00068 View details |
| 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
|
|