ClinVar Miner

List of variants in gene MYL2 reported as uncertain significance by Color Diagnostics, LLC DBA Color Health

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Total variants: 63
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HGVS dbSNP gnomAD frequency
NM_000432.4(MYL2):c.141C>A (p.Asn47Lys) rs199474808 0.00038
NM_000432.4(MYL2):c.401A>C (p.Glu134Ala) rs143139258 0.00029
NM_000432.4(MYL2):c.359G>A (p.Arg120Gln) rs192057022 0.00009
NM_000432.4(MYL2):c.374C>T (p.Thr125Met) rs375667565 0.00009
NM_000432.4(MYL2):c.433G>A (p.Asp145Asn) rs199567559 0.00005
NM_000432.4(MYL2):c.459G>C (p.Lys153Asn) rs149078011 0.00004
NM_000432.4(MYL2):c.97T>C (p.Phe33Leu) rs730880945 0.00004
NM_000432.4(MYL2):c.184A>T (p.Lys62Ter) rs201728041 0.00002
NM_000432.4(MYL2):c.256T>C (p.Phe86Leu) rs765287559 0.00002
NM_000432.4(MYL2):c.430C>G (p.Pro144Ala) rs777689913 0.00002
NM_000432.4(MYL2):c.436G>A (p.Val146Met) rs370075755 0.00002
NM_000432.4(MYL2):c.*3G>A rs530713211 0.00001
NM_000432.4(MYL2):c.101C>T (p.Thr34Ile) rs876657894 0.00001
NM_000432.4(MYL2):c.125G>A (p.Gly42Asp) rs863225117 0.00001
NM_000432.4(MYL2):c.142G>A (p.Asp48Asn) rs727504405 0.00001
NM_000432.4(MYL2):c.170G>A (p.Gly57Glu) rs199474809 0.00001
NM_000432.4(MYL2):c.206T>C (p.Met69Thr) rs2071674449 0.00001
NM_000432.4(MYL2):c.221C>T (p.Pro74Leu) rs942467544 0.00001
NM_000432.4(MYL2):c.257T>C (p.Phe86Ser) rs730880950 0.00001
NM_000432.4(MYL2):c.358C>G (p.Arg120Gly) rs397516404 0.00001
NM_000432.4(MYL2):c.413T>A (p.Met138Lys) rs748760581 0.00001
NM_000432.4(MYL2):c.422C>A (p.Ala141Asp) rs1024307408 0.00001
NM_000432.4(MYL2):c.472A>G (p.Ile158Val) rs2071648139 0.00001
NM_000432.4(MYL2):c.103A>G (p.Ile35Val) rs730880946
NM_000432.4(MYL2):c.110A>G (p.Asp37Gly) rs2136774114
NM_000432.4(MYL2):c.135C>A (p.Asp45Glu) rs199474807
NM_000432.4(MYL2):c.139A>T (p.Asn47Tyr) rs2136774049
NM_000432.4(MYL2):c.142G>C (p.Asp48His) rs727504405
NM_000432.4(MYL2):c.144T>A (p.Asp48Glu) rs2136774026
NM_000432.4(MYL2):c.151G>T (p.Asp51Tyr) rs2071683858
NM_000432.4(MYL2):c.161C>T (p.Ala54Val) rs2136773989
NM_000432.4(MYL2):c.176T>A (p.Val59Glu) rs2071674771
NM_000432.4(MYL2):c.181G>A (p.Val61Met) rs730880949
NM_000432.4(MYL2):c.188del (p.Asn63fs) rs1177936172
NM_000432.4(MYL2):c.216G>C (p.Glu72Asp) rs376506450
NM_000432.4(MYL2):c.241G>A (p.Val81Met) rs762872370
NM_000432.4(MYL2):c.275-1G>A rs764312941
NM_000432.4(MYL2):c.275-2A>G rs112557362
NM_000432.4(MYL2):c.298C>G (p.Leu100Val) rs573898913
NM_000432.4(MYL2):c.299_309del (p.Leu100fs) rs2071666850
NM_000432.4(MYL2):c.302A>G (p.Asn101Ser) rs886048960
NM_000432.4(MYL2):c.304G>T (p.Ala102Ser) rs369868176
NM_000432.4(MYL2):c.308T>G (p.Phe103Cys) rs547860537
NM_000432.4(MYL2):c.310A>C (p.Lys104Gln) rs199474811
NM_000432.4(MYL2):c.310A>G (p.Lys104Glu) rs199474811
NM_000432.4(MYL2):c.316_319del (p.Phe106fs) rs2071666714
NM_000432.4(MYL2):c.337dup (p.Val113fs)
NM_000432.4(MYL2):c.341T>G (p.Leu114Arg) rs2071666465
NM_000432.4(MYL2):c.347C>T (p.Ala116Val) rs1566148270
NM_000432.4(MYL2):c.353+6T>A rs372824804
NM_000432.4(MYL2):c.358C>T (p.Arg120Trp) rs397516404
NM_000432.4(MYL2):c.376C>G (p.Gln126Glu) rs1064796377
NM_000432.4(MYL2):c.391T>A (p.Ser131Thr)
NM_000432.4(MYL2):c.402+3A>G rs113740554
NM_000432.4(MYL2):c.424T>C (p.Phe142Leu) rs747192296
NM_000432.4(MYL2):c.430C>T (p.Pro144Ser) rs777689913
NM_000432.4(MYL2):c.431C>A (p.Pro144His) rs755993281
NM_000432.4(MYL2):c.431_432del (p.Pro144fs) rs1566147422
NM_000432.4(MYL2):c.433G>T (p.Asp145Tyr) rs199567559
NM_000432.4(MYL2):c.438dup (p.Thr147fs) rs2071649166
NM_000432.4(MYL2):c.441_442insTCACT (p.Gly148fs) rs2071649075
NM_000432.4(MYL2):c.449T>C (p.Leu150Ser) rs2071648869
NM_000432.4(MYL2):c.475A>G (p.Ile159Val) rs747098269

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