ClinVar Miner

List of variants in gene MYH3 reported as likely benign by PreventionGenetics, part of Exact Sciences

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Gene type:
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Total variants: 65
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HGVS dbSNP gnomAD frequency
NM_002470.4(MYH3):c.349-36A>G rs2285467 0.12931
NM_002470.4(MYH3):c.5160+30G>T rs73976871 0.03891
NM_002470.4(MYH3):c.3938C>T (p.Thr1313Ile) rs35230241 0.02138
NM_002470.4(MYH3):c.5796+29C>G rs570950857 0.01864
NM_002470.4(MYH3):c.4647+27G>A rs73281077 0.01783
NM_002470.4(MYH3):c.4356+11C>T rs150348272 0.00505
NM_002470.4(MYH3):c.690C>G (p.Ala230=) rs147148934 0.00421
NM_002470.4(MYH3):c.4910C>T (p.Ala1637Val) rs34165480 0.00311
NM_002470.4(MYH3):c.2926-8C>T rs188588330 0.00296
NM_002470.4(MYH3):c.3594G>A (p.Ala1198=) rs139978727 0.00252
NM_002470.4(MYH3):c.5109G>A (p.Ala1703=) rs114770362 0.00250
NM_002470.4(MYH3):c.3409C>T (p.Arg1137Cys) rs12941197 0.00245
NM_002470.4(MYH3):c.3078C>T (p.Ser1026=) rs146309217 0.00158
NM_002470.4(MYH3):c.252G>A (p.Lys84=) rs147410236 0.00156
NM_002470.4(MYH3):c.5390G>A (p.Arg1797His) rs138194008 0.00152
NM_002470.4(MYH3):c.3479C>T (p.Thr1160Met) rs145080512 0.00137
NM_002470.4(MYH3):c.2883C>A (p.Thr961=) rs144338240 0.00096
NM_002470.4(MYH3):c.4082C>T (p.Ala1361Val) rs140218185 0.00096
NM_002470.4(MYH3):c.642+10G>A rs183463746 0.00092
NM_002470.4(MYH3):c.875C>G (p.Ser292Cys) rs139480342 0.00068
NM_002470.4(MYH3):c.5658+49G>A rs138477550 0.00067
NM_002470.4(MYH3):c.736-6A>G rs372079063 0.00067
NM_002470.4(MYH3):c.3612T>C (p.Leu1204=) rs146773743 0.00063
NM_002470.4(MYH3):c.4647+6T>G rs375163919 0.00054
NM_002470.4(MYH3):c.3072C>G (p.Thr1024=) rs139544273 0.00050
NM_002470.4(MYH3):c.5301G>A (p.Ala1767=) rs151028057 0.00045
NM_002470.4(MYH3):c.1722C>T (p.Ala574=) rs149880049 0.00042
NM_002470.4(MYH3):c.2814G>A (p.Thr938=) rs147794576 0.00033
NM_002470.4(MYH3):c.3468C>T (p.Gly1156=) rs193224181 0.00023
NM_002470.4(MYH3):c.3390C>T (p.Arg1130=) rs368557407 0.00014
NM_002470.4(MYH3):c.208C>T (p.Leu70=) rs779700642 0.00012
NM_002470.4(MYH3):c.5074A>G (p.Thr1692Ala) rs140180067 0.00010
NM_002470.4(MYH3):c.505+7T>C rs779225215 0.00008
NM_002470.4(MYH3):c.5108C>T (p.Ala1703Val) rs546075871 0.00007
NM_002470.4(MYH3):c.3462G>A (p.Ala1154=) rs201553125 0.00006
NM_002470.4(MYH3):c.483C>T (p.Asn161=) rs202066674 0.00005
NM_002470.4(MYH3):c.2748C>T (p.Leu916=) rs201383580 0.00004
NM_002470.4(MYH3):c.543C>T (p.Ser181=) rs574573501 0.00004
NM_002470.4(MYH3):c.1446C>T (p.Thr482=) rs200087539 0.00002
NM_002470.4(MYH3):c.1638C>T (p.Asp546=) rs773536707 0.00002
NM_002470.4(MYH3):c.417G>C (p.Val139=) rs942862860 0.00002
NM_002470.4(MYH3):c.*5G>C
NM_002470.4(MYH3):c.1002C>T (p.Asp334=)
NM_002470.4(MYH3):c.1233C>T (p.Tyr411=)
NM_002470.4(MYH3):c.1411-243A>T
NM_002470.4(MYH3):c.1411-264A>C
NM_002470.4(MYH3):c.1411-378del
NM_002470.4(MYH3):c.1411-378dup
NM_002470.4(MYH3):c.1411-384A>T
NM_002470.4(MYH3):c.1411-389del
NM_002470.4(MYH3):c.1411-389dup
NM_002470.4(MYH3):c.1443C>T (p.Phe481=)
NM_002470.4(MYH3):c.1542C>T (p.Phe514=)
NM_002470.4(MYH3):c.1566C>T (p.Ile522=)
NM_002470.4(MYH3):c.1960-11T>A
NM_002470.4(MYH3):c.2466C>T (p.Phe822=)
NM_002470.4(MYH3):c.3445G>C (p.Glu1149Gln) rs145785711
NM_002470.4(MYH3):c.3576G>A (p.Ala1192=)
NM_002470.4(MYH3):c.3996C>T (p.His1332=)
NM_002470.4(MYH3):c.4092G>A (p.Lys1364=)
NM_002470.4(MYH3):c.4451A>G (p.Lys1484Arg) rs537656234
NM_002470.4(MYH3):c.4488T>G (p.Leu1496=) rs886038512
NM_002470.4(MYH3):c.5007G>A (p.Lys1669=)
NM_002470.4(MYH3):c.5796+32del rs147333978
NM_002470.4(MYH3):c.615G>A (p.Leu205=)

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