Variant #0000243963 (NC_000021.8:g.27264108C>T, NM_000484.3:c.2137G>A (APP))
Chromosome |
21 |
Allele |
Unknown |
Affects function (as reported) |
Affects function |
Affects function (by curator) |
Effect unknown |
Classification method |
- |
Clinical classification |
pathogenic |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.27264108C>T |
DNA change (hg38) |
g.25891796C>T |
Published as |
- |
ISCN |
- |
DB-ID |
APP_000019 See all 6 reported entries |
Variant remarks |
Detected in 1 AD patient and in 5 unaffected, aged relatives.. /r/Double point mutation in coding region. The first mutation at codon A713 causes an amino acid change. The second mutation at codon V715 is a silent mutation |
Reference |
- |
ClinVar ID |
- |
dbSNP ID |
rs63750066 |
Origin |
Unknown |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
0.0001 View details |
Owner |
Marc Cruts |
Database submission license |
Creative Commons Attribution 4.0 International |
Created by |
Julia Lopez |
Date created |
2013-05-01 13:44:57 +02:00 (CEST) |
Date last edited |
2020-07-16 21:58:29 +02:00 (CEST) |

Variant on transcripts
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