Variant #0001003338 (NC_000017.10:g.44073923G>A, NM_001123066.3:c.1720G>A (MAPT))

Chromosome 17
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.44073923G>A
DNA change (hg38) -
Published as MAPT(NM_001123066.3):c.1720G>A (p.A574T)
ISCN -
DB-ID MAPT_000007 See all 3 reported entries
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00063 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
STH NM_001007532.2 -/. - c.-2723G>A r.(?) p.(=)
MAPT NM_001123066.3 -/. - c.1720G>A r.(?) p.(Ala574Thr)
MAPT NM_016835.4 -/. - c.1666G>A r.(?) p.(Ala556Thr)


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