ClinVar Miner

List of variants in gene MYL2 reported as likely benign for Cardiomyopathy

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Total variants: 47
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HGVS dbSNP gnomAD frequency
NM_000432.4(MYL2):c.342G>A (p.Leu114=) rs199572927 0.00032
NM_000432.4(MYL2):c.275-14G>C rs375703502 0.00025
NM_000432.4(MYL2):c.243G>T (p.Val81=) rs368851472 0.00015
NM_000432.4(MYL2):c.275-7G>A rs373241541 0.00006
NM_000432.4(MYL2):c.387G>A (p.Arg129=) rs774686046 0.00006
NM_000432.4(MYL2):c.375G>A (p.Thr125=) rs190020833 0.00005
NM_000432.4(MYL2):c.216G>A (p.Glu72=) rs376506450 0.00002
NM_000432.4(MYL2):c.222G>A (p.Pro74=) rs372644111 0.00002
NM_000432.4(MYL2):c.402+6G>C rs749765328 0.00002
NM_000432.4(MYL2):c.468G>A (p.Val156=) rs137984206 0.00002
NM_000432.4(MYL2):c.474C>T (p.Ile158=) rs1423130699 0.00002
NM_000432.4(MYL2):c.147G>A (p.Leu49=) rs749936467 0.00001
NM_000432.4(MYL2):c.170-14G>C rs371431719 0.00001
NM_000432.4(MYL2):c.275-12G>A rs750937792 0.00001
NM_000432.4(MYL2):c.275-8C>T rs765328765 0.00001
NM_000432.4(MYL2):c.303C>T (p.Asn101=) rs1317472220 0.00001
NM_000432.4(MYL2):c.315G>C (p.Val105=) rs768415509 0.00001
NM_000432.4(MYL2):c.354C>T (p.Tyr118=) rs750193844 0.00001
NM_000432.4(MYL2):c.393C>G (p.Ser131=) rs778630692 0.00001
NM_000432.4(MYL2):c.403-11G>A rs1212140808 0.00001
NM_000432.4(MYL2):c.403-15G>C rs202105636 0.00001
NM_000432.4(MYL2):c.403-6T>C rs763332557 0.00001
NM_000432.4(MYL2):c.403-8C>T rs1440682502 0.00001
NM_000432.4(MYL2):c.408C>T (p.Asp136=) rs1356499130 0.00001
NM_000432.4(MYL2):c.435C>T (p.Asp145=) rs766907447 0.00001
NM_000432.4(MYL2):c.447C>T (p.Asn149=) rs397516405 0.00001
NM_000432.4(MYL2):c.450G>A (p.Leu150=) rs1379018063 0.00001
NM_000432.4(MYL2):c.483C>T (p.His161=) rs886039108 0.00001
NM_000432.4(MYL2):c.94-3C>T rs112865045 0.00001
NM_000432.4(MYL2):c.111C>T (p.Asp37=) rs1280758653
NM_000432.4(MYL2):c.135C>T (p.Asp45=) rs199474807
NM_000432.4(MYL2):c.141C>T (p.Asn47=) rs199474808
NM_000432.4(MYL2):c.156C>A (p.Thr52=) rs761358011
NM_000432.4(MYL2):c.170-20GT[3] rs764824483
NM_000432.4(MYL2):c.170-4C>T rs758237606
NM_000432.4(MYL2):c.172C>A (p.Arg58=) rs756671869
NM_000432.4(MYL2):c.174A>G (p.Arg58=) rs777225996
NM_000432.4(MYL2):c.308T>G (p.Phe103Cys) rs547860537
NM_000432.4(MYL2):c.354-8C>G rs767657562
NM_000432.4(MYL2):c.384G>A (p.Glu128=) rs1382853827
NM_000432.4(MYL2):c.417C>T (p.Phe139=) rs781107246
NM_000432.4(MYL2):c.420C>G (p.Ala140=) rs369489428
NM_000432.4(MYL2):c.420C>T (p.Ala140=) rs369489428
NM_000432.4(MYL2):c.426C>T (p.Phe142=) rs1592798603
NM_000432.4(MYL2):c.463C>T (p.Leu155=) rs1592798503
NM_000432.4(MYL2):c.480C>T (p.Thr160=) rs727505065
NM_000432.4(MYL2):c.94-10C>T rs2071684471

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