Variant #0000367928 (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 pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.45797374del
DNA change (hg38) g.45331702del
Published as 1105del; 1105delC (Ala371ProfsX23)
ISCN -
DB-ID MUTYH_000069 See all 83 reported entries
Variant remarks -
Reference DUPLICATE – to be removed
ClinVar ID -
dbSNP ID -
Origin Germline
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner InSiGHT - John-Paul Plazzer
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2018-04-06 17:05:13 +02:00 (CEST)
Date last edited 2020-06-04 13:26:31 +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.(1147del) p.(Ala385ProfsX23) -


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