ClinVar Miner

List of variants in gene MYH11 reported as uncertain significance by ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories

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Total variants: 22
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HGVS dbSNP gnomAD frequency
NM_002474.3(MYH11):c.2005C>T (p.Arg669Cys) rs111404182 0.00079
NM_002474.3(MYH11):c.2893G>T (p.Ala965Ser) rs113696032 0.00031
NM_002474.3(MYH11):c.1502G>A (p.Arg501His) rs144244239 0.00029
NM_002474.3(MYH11):c.2075C>T (p.Ala692Val) rs148893135 0.00028
NM_002474.3(MYH11):c.217A>C (p.Lys73Gln) rs147447269 0.00021
NM_002474.3(MYH11):c.3766A>C (p.Lys1256Gln) rs149241435 0.00015
NM_002474.3(MYH11):c.2724G>T (p.Glu908Asp) rs939496859 0.00004
NM_002474.3(MYH11):c.769G>A (p.Val257Met) rs112992497 0.00004
NM_002474.3(MYH11):c.935A>G (p.Asn312Ser) rs149964928 0.00004
NM_002474.3(MYH11):c.3808G>A (p.Asp1270Asn) rs770319821 0.00003
NM_002474.3(MYH11):c.3281C>T (p.Ala1094Val) rs534384552 0.00002
NM_002474.3(MYH11):c.1472T>C (p.Met491Thr) rs1236697376 0.00001
NM_002474.3(MYH11):c.1574C>T (p.Pro525Leu) rs750288554 0.00001
NM_002474.3(MYH11):c.2600G>A (p.Arg867Gln) rs773993037 0.00001
NM_002474.3(MYH11):c.3619G>A (p.Glu1207Lys) rs371831822 0.00001
NM_002474.3(MYH11):c.434A>G (p.Lys145Arg) rs755005682 0.00001
NM_002474.3(MYH11):c.534C>T (p.Gly178=) rs764984716 0.00001
NM_002474.3(MYH11):c.2057G>C (p.Arg686Thr) rs1567726588
NM_002474.3(MYH11):c.2665A>C (p.Lys889Gln) rs762308378
NM_002474.3(MYH11):c.3429C>A (p.Asp1143Glu) rs1466172600
NM_002474.3(MYH11):c.3805A>G (p.Ser1269Gly) rs200012419
NM_002474.3(MYH11):c.3839A>G (p.Asp1280Gly)

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