Variant #0000420267 (NC_000001.10:g.45796895_45796897del, NM_001128425.1:c.1437_1439del (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.45796895_45796897del
DNA change (hg38) g.45331223_45331225del
Published as 20418187_c1437_1439_binding
ISCN -
DB-ID MUTYH_000086 See all 65 reported entries
Variant remarks In vitro DNA binding assay; Expression human proteins, bacteria, glycosylase assay 8-oxoG:A; Surface plasmon resonance (SPR) real-time recording association/dissociation; severe reduction in the binding affinity
Reference PubMed: D Agostino 2010
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Astrid Out
Database submission license No license selected
Created by Astrid Out
Date created 2010-04-29 22:05:02 +02:00 (CEST)
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 +?/. 14 c.1437_1439del r.(?) p.Glu480del -


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