Variant #0000001035 (NC_000020.10:g.4680464G>A, PRNP(NM_000311.3):c.598G>A)
| Individual ID |
00001035 |
| Chromosome |
20 |
| Allele |
Unknown |
| Affects function (as reported) |
Not classified |
| Affects function (by curator) |
Not classified |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.4680464G>A |
| Reference |
Cohen OS1, Chapman J, Korczyn AD, Warman-Alaluf N, Orlev Y, Givaty G, Nitsan Z, Appel S, Rosenmann H, Kahana E, Shechter-Amir D.(2015) |
| DB-ID |
PRNP_000003 See all 10 reported entries |
| Frequency |
- |
| Average frequency (gnomAD v.2.1.1) |
0 View details |
| Owner |
Y Yang |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Y Yang |

Variant on transcripts
Screenings
|
|