Variant #0000244052 (NC_000017.10:g.44039753C>T, NM_001123066.3:c.50C>T (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.44039753C>T |
| DNA change (hg38) |
g.45962387C>T |
| Published as |
- |
| ISCN |
- |
| DB-ID |
MAPT_000012 |
| Variant remarks |
Observed in 1 African individual of the <a href=\""http://www.cephb.fr/en/hgdp/diversity.php/"""" target=blank> Human Genome Diversity Panel</a>. /r/Point mutation in coding region predicting an amino acid substitution"" |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
Unknown |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
0.00018 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 16:29:40 +02:00 (CEST) |

Variant on transcripts
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