Variant #0000243967 (NC_000021.8:g.27269954C>G, NM_000484.3:c.1995G>C (APP))
Chromosome |
21 |
Allele |
Unknown |
Affects function (as reported) |
Does not affect function |
Affects function (by curator) |
Effect unknown |
Classification method |
- |
Clinical classification |
benign |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.27269954C>G |
DNA change (hg38) |
g.25897642C>G |
Published as |
- |
ISCN |
- |
DB-ID |
APP_000022 |
Variant remarks |
Not segregating with disease. Detected in 1 patient and 1 unaffected, aged, relative.. /r/Point mutation in coding region predicting an amino acid substitution |
Reference |
- |
ClinVar ID |
- |
dbSNP ID |
rs63750363 |
Origin |
Unknown |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
1.0E-5 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 21:58:31 +02:00 (CEST) |

Variant on transcripts
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