Variant #0000291502 (NC_000017.10:g.44087741T>C, NM_001123066.3:c.1893T>C (MAPT))

Chromosome 17
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.44087741T>C
DNA change (hg38) g.46010375T>C
Published as MAPT(NM_005910.5):c.888T>C (p.N296=)
ISCN -
DB-ID MAPT_000052 See all 2 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) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-08-06 14:59:34 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
STH NM_001007532.2 +/. - c.*10709T>C r.(=) p.(=)
MAPT NM_001123066.3 +/. - c.1893T>C r.(?) p.(Asn631=)
MAPT NM_016835.4 +/. - c.1839T>C r.(?) p.(Asn613=)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.