"Revvity Omics, Revvity"[submitter] AND "MYH10"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2689490	NM_001256012.3(MYH10):c.5777G>A (p.Arg1926His)	LOC125177414, MYH10 (R1895H +3 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2461427	NM_001256012.3(MYH10):c.5303G>A (p.Arg1768Gln)	MYH10 (R1768Q +3 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2391727	NM_001256012.3(MYH10):c.4981G>A (p.Glu1661Lys)	MYH10 (E1630K +3 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2689489	NM_001256012.3(MYH10):c.4412G>A (p.Arg1471His)	MYH10 (R1440H +3 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2689488	NM_001256012.3(MYH10):c.3250C>A (p.Leu1084Met)	MYH10 (L1053M +3 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2689487	NM_001256012.3(MYH10):c.784G>A (p.Val262Ile)	MYH10 (V252I +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance

ClinVar