Variant #0000562033 (NC_000017.10:g.44068850G>A, NM_001123066.3:c.1405G>A (MAPT))

Chromosome 17
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.44068850G>A
DNA change (hg38) g.45991484G>A
Published as MAPT(NM_001123066.3):c.1405G>A (p.A469T, p.(Ala469Thr)), MAPT(NM_001123066.4):c.1405G>A (p.A469T), MAPT(NM_005910.5):c.454G>A (p.A152T)
ISCN -
DB-ID MAPT_000003 See all 5 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) 0.00145 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2024-08-28 13:16:32 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
STH NM_001007532.2 -?/. - c.-7796G>A r.(?) p.(=)
MAPT NM_001123066.3 -?/. - c.1405G>A r.(?) p.(Ala469Thr)
MAPT NM_016835.4 -?/. - c.1405G>A r.(?) p.(Ala469Thr)


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