ClinVar Miner

List of variants in gene MYO3A reported as benign for auditory system disease

Included ClinVar conditions (549):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 19
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HGVS dbSNP
NM_017433.5(MYO3A):c.-15T>A rs11014875
NM_017433.5(MYO3A):c.-18G>A rs10128298
NM_017433.5(MYO3A):c.1042A>G (p.Ile348Val) rs3824699
NM_017433.5(MYO3A):c.1053+11C>T rs3824698
NM_017433.5(MYO3A):c.1053+12A>G rs3824697
NM_017433.5(MYO3A):c.1104C>T (p.Tyr368=) rs35379457
NM_017433.5(MYO3A):c.1105G>A (p.Val369Ile) rs3817420
NM_017433.5(MYO3A):c.1170+7C>T rs3817419
NM_017433.5(MYO3A):c.2867G>A (p.Ser956Asn) rs3758449
NM_017433.5(MYO3A):c.3094G>A (p.Ala1032Thr) rs34918608
NM_017433.5(MYO3A):c.3112-4T>C rs16926628
NM_017433.5(MYO3A):c.3597G>A (p.Glu1199=) rs3740232
NM_017433.5(MYO3A):c.3850A>T (p.Thr1284Ser) rs3740231
NM_017433.5(MYO3A):c.3937C>A (p.Arg1313Ser) rs1999240
NM_017433.5(MYO3A):c.4462A>G (p.Lys1488Glu) rs34204285
NM_017433.5(MYO3A):c.480G>T (p.Thr160=) rs12257119
NM_017433.5(MYO3A):c.4848C>G (p.Ser1616=) rs56316209
NM_017433.5(MYO3A):c.533C>T (p.Thr178Ile) rs33968748
NM_017433.5(MYO3A):c.956G>A (p.Arg319His) rs3824700

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