ClinVar Miner

List of variants in gene MYH14 reported as benign by Athena Diagnostics Inc

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Gene type:
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Total variants: 19
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HGVS dbSNP gnomAD frequency
NM_001145809.2(MYH14):c.1890C>T (p.Val630=) rs77895476 0.03277
NM_001145809.2(MYH14):c.474T>C (p.Ile158=) rs34796700 0.02809
NM_001145809.2(MYH14):c.5281C>A (p.Arg1761=) rs116035034 0.02785
NM_001145809.2(MYH14):c.2041G>C (p.Gly681Arg) rs75915336 0.02765
NM_001145809.2(MYH14):c.4753-9C>T rs45591233 0.02396
NM_001145809.2(MYH14):c.3749C>A (p.Ala1250Glu) rs11669191 0.01884
NM_001145809.2(MYH14):c.3468-3C>T rs78192108 0.01724
NM_001145809.2(MYH14):c.1024C>G (p.Pro342Ala) rs34498817 0.01645
NM_001145809.2(MYH14):c.483G>A (p.Met161Ile) rs34773557 0.01615
NM_001145809.2(MYH14):c.4596C>T (p.Ala1532=) rs35453633 0.01258
NM_001145809.2(MYH14):c.2841C>T (p.Arg947=) rs138987081 0.01050
NM_001145809.2(MYH14):c.5466G>A (p.Leu1822=) rs10419343 0.01020
NM_001145809.2(MYH14):c.4255C>T (p.Arg1419Trp) rs115019972 0.00553
NM_001145809.2(MYH14):c.2792G>A (p.Arg931His) rs200351672 0.00460
NM_001145809.2(MYH14):c.2763A>G (p.Lys921=) rs191788683 0.00404
NM_001145809.2(MYH14):c.1944C>T (p.Asp648=) rs189243324 0.00120
NM_001145809.2(MYH14):c.1224C>T (p.Leu408=) rs145163585 0.00037
NM_001145809.2(MYH14):c.192G>T (p.Gly64=) rs181055215
NM_001145809.2(MYH14):c.33G>C (p.Arg11=) rs8106196

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