"PreventionGenetics, part of Exact Sciences"[submitter] AND "MYO18A"[g - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3047824	NM_078471.4(MYO18A):c.6134_6135del (p.Thr2045fs)	MYO18A (T1572fs +5 more)	Microsatellite (frameshift variant)	MYO18A-related disorder	GLikely benign
Select item 2629676	NM_078471.4(MYO18A):c.5410G>T (p.Val1804Leu)	MYO18A (V1346L +4 more)	Single nucleotide variant (missense variant)	MYO18A-related disorder	GUncertain significance
Select item 3046335	NM_078471.4(MYO18A):c.5207G>A (p.Arg1736His)	MYO18A (R1278H +4 more)	Single nucleotide variant (missense variant)	MYO18A-related disorder	GLikely benign
Select item 790718	NM_078471.4(MYO18A):c.3770G>A (p.Arg1257Gln)	MYO18A (R1257Q +3 more)	Single nucleotide variant (missense variant)	not provided +1 more	GLikely benign
Select item 3040314	NM_078471.4(MYO18A):c.970G>A (p.Gly324Ser)	MYO18A (G324S)	Single nucleotide variant (missense variant)	MYO18A-related disorder	GLikely benign
Select item 3032007	NM_078471.4(MYO18A):c.39C>T (p.Gly13=)	MYO18A	Single nucleotide variant (synonymous variant)	MYO18A-related disorder	GLikely benign

ClinVar