Variant #0001046792 (NC_000021.8:g.27423376G>A, NM_000484.3:c.602C>T (APP))
| Chromosome |
21 |
| Allele |
Unknown |
| Affects function (as reported) |
Probably does not affect function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
likely benign |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.27423376G>A |
| DNA change (hg38) |
- |
| Published as |
APP(NM_000484.3):c.602C>T (p.(Ala201Val)) |
| ISCN |
- |
| DB-ID |
APP_000090 |
| Variant remarks |
VKGL data sharing initiative Nederland |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
CLASSIFICATION record |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
0.00012 View details |
| Owner |
VKGL-NL_Leiden |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Leiden |
| Date created |
2025-07-08 13:22:38 +02:00 (CEST) |
| Date last edited |
N/A |

Variant on transcripts
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