Variant #0000616641 (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) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.44068928G>A
DNA change (hg38) g.45991562G>A
Published as MAPT(NM_005910.5):c.532G>A (p.A178T), MAPT(NM_005910.6):c.532G>A (p.A178T)
ISCN -
DB-ID MAPT_000025 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) 0.00355 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
STH NM_001007532.2 -/. - c.-7718G>A r.(?) p.(=)
MAPT NM_001123066.3 -/. - c.1483G>A r.(?) p.(Ala495Thr)
MAPT NM_016835.4 -/. - c.1483G>A r.(?) p.(Ala495Thr)


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