Full data view for gene MUTYH


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

2 entries on 1 page. Showing entries 1 - 2.
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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

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P-domain     

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DNA change (genomic) (hg19)     

DNA change (hg38)     

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ISCN     

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Owner     
?/. 8i c.691-1G>A r.(691_788del) p.(Ala231GlyfsX65) - Unknown - VUS g.45798161C>T g.45332489C>T 649-1G>A (Ala217GlyfsX65) - MUTYH_000014 - DUPLICATE – to be removed - - Germline - - - - - - - - - - - - - - - - - - - - - - -
?/. 8i c.691-1G>A r.(691_788del) p.(Ala231GlyfsX65) - Parent #2 - VUS g.45798161C>T g.45332489C>T 649-1G>A (Ala217GlyfsX65) - MUTYH_000014 Alamut: acceptor splice site of intron 8 affected; skip exon 9 very likely (or retaining of intron 9 possible? Also strong acceptor at c.691-32 and new stong acceptor at c.692) PubMed: Nielsen 2005; PubMed: Nielsen 2007; PubMed: Nielsen 2009a; PubMed: Nielsen 2009b; PubMed: Vogt 2009 - - Germline - - - - - DNA DGGE, SEQ leukocyte screen MUTYH gene (index) ? - PubMed: Nielsen 2005, PubMed: Nielsen 2007, PubMed: Nielsen 2009a, PubMed: Nielsen 2009b, PubMed: Vogt 2009 Among 170 APC negative Dutch FAP patients F - Netherlands - - - - - 1 Carli Tops
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