Variant #0000000097 (NC_000021.8:g.27264167T>C, APP(NM_000484.3):c.2078A>G)
| Individual ID |
00000097 |
| Chromosome |
21 |
| Allele |
Unknown |
| Affects function (as reported) |
Not classified |
| Affects function (by curator) |
Not classified |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.27264167T>C |
| Reference |
Kamino K1, Orr HT, Payami H, Wijsman EM, Alonso ME, Pulst SM, Anderson L, O'dahl S, Nemens E, White JA, et al.(1992) |
| DB-ID |
APP_000006 See all 2 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
|