Variant #0000279603 (NC_000017.10:g.44061023G>A, NM_001123066.3:c.853G>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.44061023G>A
DNA change (hg38) g.45983657G>A
Published as MAPT(NM_001123066.4):c.853G>A (p.D285N), MAPT(NM_001377265.1):c.1078G>A (p.D360N)
ISCN -
DB-ID MAPT_000018 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) 0.14544 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2025-05-05 21:14:00 +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.-15623G>A r.(?) p.(=)
MAPT NM_001123066.3 -/. - c.853G>A r.(?) p.(Asp285Asn)
MAPT NM_016835.4 -/. - c.853G>A r.(?) p.(Asp285Asn)


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