ClinVar Miner

Submissions for variant NM_001197104.1(KMT2A):c.4367A>G (p.His1456Arg) (rs1131691433)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000493938 SCV000582112 likely pathogenic not provided 2015-09-05 criteria provided, single submitter clinical testing The H1456R variant in the KMT2A gene has not been published as a pathogenic variant, nor has it been reported as a benign polymorphism to our knowledge. The H1456R variant was not observed in approximately 6500 individuals of European and African American ancestry in the NHLBI Exome Sequencing Project, indicating it is not a common benign variant in these populations. The H1456R variant is a conservative amino acid substitution, which is not likely to impact secondary protein structure as these residues share similar properties. This substitution occurs at a position that is conserved across species. In silico analysis predicts this variant is probably damaging to the protein structure/function. One missense variant in a nearby residue (C1448R) has been reported in the Human Gene Mutation Database in association with atypical Wiedemann-Steiner syndrome (Stenson et al., 2014), supporting the functional importance of this region of the protein. The H1456R variant is a strong candidate for a disease-causing variant however the possibility it may be a rare benign variant cannot be excluded.
Mendelics RCV000988751 SCV001138602 likely pathogenic Wiedemann-Steiner syndrome 2019-05-28 criteria provided, single submitter clinical testing

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