Variant #0000420199 (NC_000001.10:g.45800156C>T, NM_001128425.1:c.64G>A (MUTYH))

Chromosome 1
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.45800156C>T
DNA change (hg38) g.45334484C>T
Published as 18534194_protein_V22M
ISCN -
DB-ID MUTYH_000005 See all 79 reported entries
Variant remarks Protein expression assay; GST-tagged 535 amino acid human MUTYH expressed from vector in E.Coli; Sodium dodecyl sulfateƱPAGE analysis for protein weight; Western blot; Molecular weight similar to the number of codons exprected to be expressed
Reference PubMed: Ali 2008
ClinVar ID -
dbSNP ID rs3219484
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.04874 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 21:54:44 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

P-domain     
MUTYH NM_001128425.1 ?/. 2 c.64G>A r.(?) p.Val22Met -


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