Variant #0000000099 (NC_000021.8:g.27264108C>T, APP(NM_000484.3):c.2137G>A)
Individual ID |
00000099 |
Chromosome |
21 |
Allele |
Unknown |
Affects function (as reported) |
Not classified |
Affects function (by curator) |
Not classified |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.27264108C>T |
Reference |
Rossi G1, Giaccone G, Maletta R, Morbin M, Capobianco R, Mangieri M, Giovagnoli AR, Bizzi A, Tomaino C, Perri M, Di Natale M, Tagliavini F, Bugiani O, Bruni AC.(2004) |
DB-ID |
APP_000008 See all 2 reported entries |
Frequency |
XYZ19940216 |
Average frequency (gnomAD v.2.1.1) |
0.0001 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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