Variant #0000616640 (NC_000017.10:g.44060834C>A, NM_001123066.3:c.664C>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.44060834C>A
DNA change (hg38) g.45983468C>A
Published as MAPT(NM_001123066.3):c.664C>A (p.R222S), MAPT(NM_001123066.4):c.664C>A (p.R222S)
ISCN -
DB-ID MAPT_000093 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) 0.00028 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
STH NM_001007532.2 -?/. - c.-15812C>A r.(?) p.(=)
MAPT NM_001123066.3 -?/. - c.664C>A r.(?) p.(Arg222Ser)
MAPT NM_016835.4 -?/. - c.664C>A r.(?) p.(Arg222Ser)


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