Variant #0000420170 (NC_000001.10:g.45797846G>A, NM_001128425.1:c.925C>T (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.45797846G>A
DNA change (hg38) g.45332174G>A
Published as 20848659_R281C
ISCN -
DB-ID MUTYH_000019 See all 24 reported entries
Variant remarks in vitro test of the DNA glycosylase activity on adenine mispaired with 8-hydroxyguanine; glycosylase activity as wildtype
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) 0.00046 View details
Owner Carli Tops
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Carli Tops
Date created 2010-10-07 20:19:43 +02:00 (CEST)
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 ?/. 10 c.925C>T r.(?) p.Arg309Cys -


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