ClinVar Miner

List of variants in gene MYO3A reported as benign for not specified

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Gene type:
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Total variants: 46
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HGVS dbSNP gnomAD frequency
NM_017433.5(MYO3A):c.1105G>A (p.Val369Ile) rs3817420 0.69434
NM_017433.5(MYO3A):c.1042A>G (p.Ile348Val) rs3824699 0.68769
NM_017433.5(MYO3A):c.3937C>A (p.Arg1313Ser) rs1999240 0.60118
NM_017433.5(MYO3A):c.2867G>A (p.Ser956Asn) rs3758449 0.51636
NM_017433.5(MYO3A):c.1170+7C>T rs3817419 0.47630
NM_017433.5(MYO3A):c.956G>A (p.Arg319His) rs3824700 0.47622
NM_017433.5(MYO3A):c.1104C>T (p.Tyr368=) rs35379457 0.47540
NM_017433.5(MYO3A):c.1053+11C>T rs3824698 0.47508
NM_017433.5(MYO3A):c.1053+12A>G rs3824697 0.47492
NM_017433.5(MYO3A):c.3850A>T (p.Thr1284Ser) rs3740231 0.39847
NM_017433.5(MYO3A):c.3597G>A (p.Glu1199=) rs3740232 0.31670
NM_017433.5(MYO3A):c.3112-4T>C rs16926628 0.12937
NM_017433.5(MYO3A):c.1743G>A (p.Glu581=) rs41279908 0.10116
NM_017433.5(MYO3A):c.4438+18T>C rs17739680 0.10011
NM_017433.5(MYO3A):c.480G>T (p.Thr160=) rs12257119 0.09365
NM_017433.5(MYO3A):c.-15T>A rs11014875 0.08552
NM_017433.5(MYO3A):c.624C>T (p.Asp208=) rs35010955 0.08016
NM_017433.5(MYO3A):c.660C>T (p.Ala220=) rs34067308 0.06790
NM_017433.5(MYO3A):c.731+20G>A rs56210104 0.06778
NM_017433.5(MYO3A):c.2497G>T (p.Ala833Ser) rs33947968 0.06209
NM_017433.5(MYO3A):c.4848C>G (p.Ser1616=) rs56316209 0.02444
NM_017433.5(MYO3A):c.4335A>G (p.Lys1445=) rs34615182 0.01332
NM_017433.5(MYO3A):c.533C>T (p.Thr178Ile) rs33968748 0.01220
NM_017433.5(MYO3A):c.3028G>A (p.Glu1010Lys) rs61729833 0.00965
NM_017433.5(MYO3A):c.3094G>A (p.Ala1032Thr) rs34918608 0.00845
NM_017433.5(MYO3A):c.3859C>A (p.Pro1287Thr) rs35575696 0.00819
NM_017433.5(MYO3A):c.4250C>T (p.Thr1417Ile) rs34151474 0.00780
NM_017433.5(MYO3A):c.3408C>T (p.Phe1136=) rs61731629 0.00612
NM_017433.5(MYO3A):c.4465A>G (p.Ile1489Val) rs147376000 0.00541
NM_017433.5(MYO3A):c.1971T>C (p.Thr657=) rs112195128 0.00489
NM_017433.5(MYO3A):c.2169T>C (p.Asn723=) rs114982270 0.00462
NM_017433.5(MYO3A):c.3589G>A (p.Glu1197Lys) rs75801377 0.00414
NM_017433.5(MYO3A):c.1777-14G>T rs4592324 0.00409
NM_017433.5(MYO3A):c.949G>C (p.Ala317Pro) rs61731652 0.00334
NM_017433.5(MYO3A):c.4589A>T (p.Gln1530Leu) rs147749053 0.00236
NM_017433.5(MYO3A):c.1559C>T (p.Ala520Val) rs72787346 0.00218
NM_017433.5(MYO3A):c.2973G>T (p.Arg991=) rs146647767 0.00204
NM_017433.5(MYO3A):c.4462A>G (p.Lys1488Glu) rs34204285 0.00134
NM_017433.5(MYO3A):c.4439-12C>T rs201689300 0.00126
NM_017433.5(MYO3A):c.1242A>T (p.Gly414=) rs3758442 0.00083
NM_017433.5(MYO3A):c.2133G>A (p.Leu711=) rs56147819 0.00078
NM_017433.5(MYO3A):c.3584T>C (p.Val1195Ala) rs35675577 0.00039
NM_017433.5(MYO3A):c.3133G>A (p.Val1045Met) rs35447806 0.00005
NM_017433.5(MYO3A):c.1053+11_1053+12inv
NM_017433.5(MYO3A):c.1104_1105delinsTA (p.Val369Ile) rs386742102
NM_017433.5(MYO3A):c.409-21TA[2] rs112520797

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