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
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