Variant #0000000105 (NC_000021.8:g.27264095A>C, APP(NM_000484.3):c.2150T>G)
Individual ID |
00000105 |
Chromosome |
21 |
Allele |
Unknown |
Affects function (as reported) |
Not classified |
Affects function (by curator) |
Not classified |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.27264095A>C |
Reference |
Chartier-Harlin MC1, Crawford F, Houlden H, Warren A, Hughes D, Fidani L, Goate A, Rossor M, Roques P, Hardy J, et al.(1991) |
DB-ID |
APP_000014 See all 4 reported entries |
Frequency |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
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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