Variant #0000420139 (NC_000001.10:g.45798117C>T, NM_001128425.1:c.734G>A (MUTYH))

Chromosome 1
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.45798117C>T
DNA change (hg38) g.45332445C>T
Published as 18534194_binding_R231H
ISCN -
DB-ID MUTYH_000051 See all 37 reported entries
Variant remarks DNA binding assay; GST-tagged 535 amino acid human MUTYH; gel mobility shift assays for DNA binding; absent substrate binding
Reference PubMed: Ali 2008
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 8.0E-5 View details
Owner Astrid Out
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Astrid Out
Date created 2010-02-09 11:21:32 +01:00 (CET)
Date last edited 2020-07-14 21:57:48 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

P-domain     
MUTYH NM_001128425.1 +/. 9 c.734G>A r.(?) p.Arg245His -


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