Variant #0000000199 (NC_000001.10:g.227071449G>A, PSEN2(NM_000447.2):c.185G>A)
Individual ID |
00000199 |
Chromosome |
1 |
Allele |
Unknown |
Affects function (as reported) |
Not classified |
Affects function (by curator) |
Not classified |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.227071449G>A |
Reference |
Cruts M1, van Duijn CM, Backhovens H, Van den Broeck M, Wehnert A, Serneels S, Sherrington R, Hutton M, Hardy J, St George-Hyslop PH, Hofman A, Van Broeckhoven C.(1998) |
DB-ID |
PSEN2_000001 See all 2 reported entries |
Frequency |
- |
Average frequency (gnomAD v.2.1.1) |
0.00856 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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