ClinVar Miner

Submissions for variant NM_000257.4(MYH7):c.748A>T (p.Ile250Phe) (rs397516268)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000158762 SCV000208697 likely pathogenic not provided 2012-03-29 criteria provided, single submitter clinical testing p.Ile250Phe (ATT>TTT): c.748 A>T in exon 9 of the MYH7 gene. The Ile250Phe variant in the MYH7 gene has not been reported previously as a disease-causing mutation or as a benign polymorphism, to our knowledge. Ile250Phe results in a non-conservative amino acid substitution of a smaller hydrophobic Isoleucine with a larger hydrophobic Phenylalanine residue at a position that is highly conserved throughout evolution. Mutations in nearby codons (Phe247Leu, Arg249Gln, His251Asn) have been reported in association with HCM, further supporting the functional importance of this region of the protein. Furthermore, in silico analysis predicts Ile250Phe is probably damaging to the protein structure/function (Adzhubei et al., 2000; Schwarz et al., 2011). The NHLBI ESP Exome Variant Server reports Ile250Phe was not observed in approximately 5,000 samples from individuals of European and African American backgrounds, indicating it is not a common benign variant in these populations (NHLBI ESP). Therefore, while Ile250Phe is a good candidate for a disease-causing mutation, we cannot unequivocally determine the clinical significance of this variant with the clinical and molecular information available at this time. The variant is found in HCM panel(s).

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