All variants in the MUTYH gene


Information The variants shown are described using the NM_001128425.1 transcript reference sequence.

3 entries on 1 page. Showing entries 1 - 3.
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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

P-domain     

Classification method     

Clinical classification     

DNA change (genomic) (hg19)     

DNA change (hg38)     

Published as     

ISCN     

DB-ID     

Variant remarks     

Reference     

ClinVar ID     

dbSNP ID     

Origin     

Segregation     

Frequency     

Re-site     

VIP     

Methylation     

Owner     
?/. 1 c.20G>A r.(20g>a) p.(Arg7His) - - VUS g.45805907C>T g.45340235C>T 20G>A (Arg7His) - MUTYH_000256 - DUPLICATE – to be removed - - Germline - - - 0 - InSiGHT - John-Paul Plazzer
?/. 1 c.20G>A r.(20g>a) p.(Arg7His) - - VUS g.45805907C>T g.45340235C>T 20G>A (Arg7His) - MUTYH_000256 - Clinical Biochemistry, Hvidovre Hospital, Hvidovre, DK - - Unknown - - - 0 - Rikke Veggerby Groenlund
?/. - c.20G>A r.(?) p.(Arg7His) - - NA g.45805907C>T - chr1_45805907_C_T - MUTYH_000256 not in 60466 cases; the study was not designed to clinically classify individual variants but performed burden-type association analyses, grouping certain variant types PubMed: Dorling 2021, Journal: Dorling 2021 - - Germline - 1/53461 controls - 0 - BRIDGES consortium
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