"Baylor Genetics"[submitter] AND "MYO5B"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 740504	NM_001080467.3(MYO5B):c.3001A>T (p.Ile1001Phe)	MYO5B (I1001F)	Single nucleotide variant (missense variant)	Congenital microvillous atrophy +1 more	GConflicting classifications of pathogenicity
Select item 1031041	NM_001080467.3(MYO5B):c.2641C>T (p.Gln881Ter)	MYO5B (Q881*)	Single nucleotide variant (nonsense)	Congenital microvillous atrophy +1 more	GPathogenic