ClinVar Miner

List of variants in gene MYH3 reported by Ambry Genetics

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Total variants: 59
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HGVS dbSNP gnomAD frequency
NM_002470.4(MYH3):c.5390G>A (p.Arg1797His) rs138194008 0.00152
NM_002470.4(MYH3):c.166C>G (p.Gln56Glu) rs143973840 0.00058
NM_002470.4(MYH3):c.3137G>A (p.Arg1046Gln) rs142002449 0.00028
NM_002470.4(MYH3):c.4109C>T (p.Ala1370Val) rs200964415 0.00017
NM_002470.4(MYH3):c.4321G>A (p.Ala1441Thr) rs190551597 0.00017
NM_002470.4(MYH3):c.4925A>G (p.Lys1642Arg) rs143396252 0.00012
NM_002470.4(MYH3):c.1880C>T (p.Thr627Met) rs370119974 0.00007
NM_002470.4(MYH3):c.5233G>A (p.Ala1745Thr) rs754751938 0.00006
NM_002470.4(MYH3):c.2486C>T (p.Pro829Leu) rs200652175 0.00004
NM_002470.4(MYH3):c.3527G>T (p.Arg1176Leu) rs143550129 0.00004
NM_002470.4(MYH3):c.3593C>T (p.Ala1198Val) rs374929326 0.00004
NM_002470.4(MYH3):c.4543G>C (p.Glu1515Gln) rs370151413 0.00004
NM_002470.4(MYH3):c.892C>T (p.Leu298Phe) rs367711644 0.00004
NM_002470.4(MYH3):c.3344G>A (p.Arg1115Gln) rs748991696 0.00003
NM_002470.4(MYH3):c.256G>A (p.Asp86Asn) rs779714194 0.00001
NM_002470.4(MYH3):c.1077C>G (p.His359Gln)
NM_002470.4(MYH3):c.1211G>C (p.Arg404Thr) rs886052584
NM_002470.4(MYH3):c.1249A>T (p.Thr417Ser)
NM_002470.4(MYH3):c.173G>T (p.Gly58Val)
NM_002470.4(MYH3):c.1895G>A (p.Ser632Asn)
NM_002470.4(MYH3):c.2109C>G (p.Ile703Met)
NM_002470.4(MYH3):c.2300A>G (p.Lys767Arg)
NM_002470.4(MYH3):c.2342G>A (p.Arg781His)
NM_002470.4(MYH3):c.2555C>T (p.Thr852Ile)
NM_002470.4(MYH3):c.2867A>C (p.Asp956Ala)
NM_002470.4(MYH3):c.2867A>G (p.Asp956Gly)
NM_002470.4(MYH3):c.2868T>G (p.Asp956Glu)
NM_002470.4(MYH3):c.3017A>G (p.Gln1006Arg)
NM_002470.4(MYH3):c.3269A>C (p.Gln1090Pro) rs1555525941
NM_002470.4(MYH3):c.3391G>A (p.Ala1131Thr)
NM_002470.4(MYH3):c.3394A>G (p.Lys1132Glu)
NM_002470.4(MYH3):c.3486A>G (p.Ile1162Met)
NM_002470.4(MYH3):c.3502C>T (p.Arg1168Trp)
NM_002470.4(MYH3):c.353A>G (p.Tyr118Cys)
NM_002470.4(MYH3):c.3718T>A (p.Ser1240Thr) rs752510156
NM_002470.4(MYH3):c.3751C>T (p.Arg1251Ter)
NM_002470.4(MYH3):c.3830A>G (p.Gln1277Arg)
NM_002470.4(MYH3):c.3859G>A (p.Glu1287Lys)
NM_002470.4(MYH3):c.3935A>G (p.Gln1312Arg)
NM_002470.4(MYH3):c.4018G>A (p.Asp1340Asn)
NM_002470.4(MYH3):c.4030C>A (p.Leu1344Met)
NM_002470.4(MYH3):c.4430C>T (p.Ser1477Phe)
NM_002470.4(MYH3):c.4475C>T (p.Ala1492Val)
NM_002470.4(MYH3):c.4502G>A (p.Arg1501Gln)
NM_002470.4(MYH3):c.4760T>C (p.Leu1587Pro)
NM_002470.4(MYH3):c.4820G>A (p.Arg1607Gln)
NM_002470.4(MYH3):c.5021T>C (p.Ile1674Thr)
NM_002470.4(MYH3):c.5179A>G (p.Thr1727Ala)
NM_002470.4(MYH3):c.5279T>C (p.Ile1760Thr)
NM_002470.4(MYH3):c.5387A>G (p.His1796Arg)
NM_002470.4(MYH3):c.5404G>A (p.Glu1802Lys)
NM_002470.4(MYH3):c.5468T>G (p.Leu1823Arg)
NM_002470.4(MYH3):c.5536C>T (p.Arg1846Trp)
NM_002470.4(MYH3):c.5605_5659-47del rs1555524879
NM_002470.4(MYH3):c.5722G>C (p.Glu1908Gln)
NM_002470.4(MYH3):c.5774C>G (p.Thr1925Ser)
NM_002470.4(MYH3):c.706A>C (p.Thr236Pro) rs1555527172
NM_002470.4(MYH3):c.755A>T (p.His252Leu)
NM_002470.4(MYH3):c.856A>G (p.Ile286Val)

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