Variant #0000243979 (NC_000017.10:g.41423219T>C, NM_001123066.3:c.1321T>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.41423219T>C |
DNA change (hg38) |
g.43345851T>C |
Published as |
- |
ISCN |
- |
DB-ID |
MAPT_000022 See all 5 reported entries |
Variant remarks |
Point mutation in coding region predicting an amino acid substitution |
Reference |
- |
ClinVar ID |
- |
dbSNP ID |
rs2258689 |
Origin |
Unknown |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
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 |
N/A |

Variant on transcripts
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