ClinVar Miner

List of variants reported as likely benign for Methylmalonic aciduria due to methylmalonyl-CoA mutase deficiency by Genomic Medicine Center of Excellence, King Faisal Specialist Hospital and Research Centre

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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_000255.4(MMUT):c.1091A>C (p.Tyr364Ser)	rs563776413	0.00002
NM_000255.4(MMUT):c.1091A>G (p.Tyr364Cys)	rs563776413

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