Variant #0000420168 (NC_000001.10:g.45797356A>G, NM_001128425.1:c.1163T>C (MUTYH))

Chromosome 1
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.45797356A>G
DNA change (hg38) g.45331684A>G
Published as 20848659_L360P
ISCN -
DB-ID MUTYH_000071 See all 5 reported entries
Variant remarks in vitro test of the DNA glycosylase activity on adenine mispaired with 8-hydroxyguanine; extremely severely defective
Reference PubMed: Goto 2010
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Carli Tops
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Carli Tops
Date created 2010-12-22 15:00:41 +01:00 (CET)
Date last edited 2020-07-14 21:56:45 +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 +?/. 12 c.1163T>C r.(?) p.Leu388Pro -


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