List of variants in gene MYH14 reported as uncertain significance by ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 20

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HGVS	dbSNP	gnomAD frequency
NM_001145809.2(MYH14):c.820A>G (p.Ile274Val)	rs200424400	0.00027
NM_001145809.2(MYH14):c.3098C>T (p.Thr1033Met)	rs201746408	0.00015
NM_001145809.2(MYH14):c.526G>A (p.Ala176Thr)	rs138001307	0.00014
NM_001145809.2(MYH14):c.1067C>T (p.Thr356Met)	rs151082668	0.00011
NM_001145809.2(MYH14):c.266T>C (p.Leu89Pro)	rs988356194	0.00011
NM_001145809.2(MYH14):c.2651A>G (p.Tyr884Cys)	rs373457292	0.00009
NM_001145809.2(MYH14):c.4156A>T (p.Thr1386Ser)	rs377462520	0.00009
NM_001145809.2(MYH14):c.3433C>T (p.Arg1145Trp)	rs773117828	0.00006
NM_001145809.2(MYH14):c.4219C>T (p.Arg1407Cys)	rs535145284	0.00006
NM_001145809.2(MYH14):c.2458C>T (p.Arg820Cys)	rs767984672	0.00005
NM_001145809.2(MYH14):c.1381C>T (p.Arg461Cys)	rs752732851	0.00003
NM_001145809.2(MYH14):c.1418G>A (p.Arg473His)	rs199812021	0.00003
NM_001145809.2(MYH14):c.5963G>A (p.Arg1988His)	rs376315069	0.00003
NM_001145809.2(MYH14):c.4615C>T (p.Arg1539Cys)	rs770767114	0.00002
NM_001145809.2(MYH14):c.4307G>A (p.Arg1436Gln)	rs773527189	0.00001
NM_001145809.2(MYH14):c.4921C>T (p.Arg1641Cys)	rs748898201	0.00001
NM_001145809.2(MYH14):c.5875C>T (p.Arg1959Trp)	rs758424787	0.00001
NM_001145809.2(MYH14):c.2988C>G (p.Ser996Arg)	rs368160641
NM_001145809.2(MYH14):c.5975C>T (p.Thr1992Ile)	rs1555779737
NM_001145809.2(MYH14):c.6074C>T (p.Pro2025Leu)	rs772690371

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