Variant #0000243977 (NC_000017.10:g.44061036T>C, NM_001123066.3:c.866T>C (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.44061036T>C |
DNA change (hg38) |
g.45983670T>C |
Published as |
- |
ISCN |
- |
DB-ID |
MAPT_000020 See all 3 reported entries |
Variant remarks |
Point mutation in coding region predicting an amino acid substitution |
Reference |
- |
ClinVar ID |
- |
dbSNP ID |
rs62063787 |
Origin |
Unknown |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
0.14545 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 16:29:54 +02:00 (CEST) |

Variant on transcripts
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