Variant #0000243981 (NC_000017.10:g.44068924G>A, NM_001123066.3:c.1479G>A (MAPT))
| Chromosome |
17 |
| 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.44068924G>A |
| DNA change (hg38) |
g.45991558G>A |
| Published as |
- |
| ISCN |
- |
| DB-ID |
MAPT_000024 See all 5 reported entries |
| Variant remarks |
Silent point mutation in coding region |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
rs1052551 |
| Origin |
Unknown |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
0.14484 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 |
2020-07-13 16:30:10 +02:00 (CEST) |

Variant on transcripts
|
Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.
|