Variant #0000243982 (NC_000017.10:g.44068928G>A, NM_001123066.3:c.1483G>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.44068928G>A
DNA change (hg38) g.45991562G>A
Published as -
ISCN -
DB-ID MAPT_000025 See all 3 reported entries
Variant remarks Not segregating with disease: Detected in 1 patient but not in 1 affected relative.. /r/Point mutation in coding region predicting an amino acid substitution
Reference -
ClinVar ID -
dbSNP ID rs63750612
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00355 View details
Owner Marc Cruts
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by Julia Lopez
Date created 2013-05-01 13:44:57 +02:00 (CEST)
Date last edited 2020-07-13 16:30:11 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MAPT NM_001123066.3 -/? 9 c.1483G>A r.(?) p.(Ala495Thr)


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