Variant #0000420257 (NC_000001.10:g.45797374del, NM_001128425.1:c.1147del (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.45797374del
DNA change (hg38) g.45331702del
Published as 15987719_binding_G396D_1147del
ISCN -
DB-ID MUTYH_000069 See all 83 reported entries
Variant remarks DNA binding assay; Patient derived lymphoblastoid cell line; UV A:GO and AO:G binding assay (relatively specific for MUTYH); Reduction in substate binding (similar to reduction in protein expression), 40-50% of WT; residual binding probably from G396D allele
Reference PubMed: Parker 2005
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 2010-02-09 11:21:32 +01:00 (CET)
Date last edited 2020-07-14 21:57:48 +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.1147del r.(?) p.Ala385Profs*23 -


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