List of variants in gene MYH14 reported by OMIM

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_001145809.2(MYH14):c.1150G>T (p.Gly384Cys)	rs119103280	0.00303
NM_001145809.2(MYH14):c.20C>A (p.Ser7Ter)	rs119103279
NM_001145809.2(MYH14):c.2299C>A (p.Arg767Ser)	rs28940307
NM_001145809.2(MYH14):c.2921G>T (p.Arg974Leu)	rs113993956
NM_001145809.2(MYH14):c.3049C>T (p.Leu1017Phe)	rs28940306
NM_001145809.2(MYH14):c.359C>T (p.Ser120Leu)	rs119103281

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