ClinVar Miner

List of variants in gene MYH14 reported as benign for not provided

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Total variants: 20
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HGVS dbSNP
NM_001145809.2(MYH14):c.1024C>G (p.Pro342Ala) rs34498817
NM_001145809.2(MYH14):c.1115-71G>A
NM_001145809.2(MYH14):c.1210+58C>T
NM_001145809.2(MYH14):c.1890C>T (p.Val630=) rs77895476
NM_001145809.2(MYH14):c.2232+86T>C
NM_001145809.2(MYH14):c.2354+47C>T
NM_001145809.2(MYH14):c.2359G>A (p.Glu787Lys) rs397516628
NM_001145809.2(MYH14):c.2695-90G>A
NM_001145809.2(MYH14):c.2763A>G (p.Lys921=) rs191788683
NM_001145809.2(MYH14):c.2841C>T (p.Arg947=) rs138987081
NM_001145809.2(MYH14):c.3034-85G>A
NM_001145809.2(MYH14):c.3537C>T (p.Ala1179=) rs559356437
NM_001145809.2(MYH14):c.3749C>A (p.Ala1250Glu) rs11669191
NM_001145809.2(MYH14):c.4032+52G>C
NM_001145809.2(MYH14):c.483G>A (p.Met161Ile) rs34773557
NM_001145809.2(MYH14):c.5281C>A (p.Arg1761=) rs116035034
NM_001145809.2(MYH14):c.5466G>A (p.Leu1822=) rs10419343
NM_001145809.2(MYH14):c.5529C>T (p.Ser1843=) rs12610591
NM_001145809.2(MYH14):c.5868C>T (p.Ala1956=) rs190695624
NM_024729.3:c.4629+16G>A

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