ClinVar Miner

Submissions for variant NM_000255.4(MMUT):c.754C>T (p.His252Tyr) (rs796052010)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000186063 SCV000239027 uncertain significance not provided 2014-11-03 criteria provided, single submitter clinical testing p.His252Tyr (CAC>TAC): c.754 C>T in exon 4 of the MUT gene (NM_000255.3). The H252Y variant has not been published as a mutation, nor has it been reported as a benign polymorphism to our knowledge. The H252Y variant is a non-conservative amino acid substitution, which is likely to impact secondary protein structure as these residues differ in polarity, charge, size and/or other properties. This substitution occurs at a position that is moderately conserved across species. In silico analysis is inconsistent in its predictions as to whether or not the variant is damaging to the protein structure/function. Therefore, based on the currently available information, it is unclear whether this variant is a pathogenic mutation or a rare benign variant. The variant is found in MMA-MET panel(s).

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