ClinVar Miner

List of variants in gene MYO3A reported as uncertain significance for not specified

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Total variants: 44
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HGVS dbSNP gnomAD frequency
NM_017433.5(MYO3A):c.170A>C (p.Asp57Ala) rs146511800 0.00094
NM_017433.5(MYO3A):c.3037C>T (p.Arg1013Cys) rs140154015 0.00049
NM_017433.5(MYO3A):c.1174T>C (p.Ser392Pro) rs201323717 0.00034
NM_017433.5(MYO3A):c.2275A>T (p.Asn759Tyr) rs201033926 0.00030
NM_017433.5(MYO3A):c.426T>G (p.His142Gln) rs189595832 0.00029
NM_017433.5(MYO3A):c.2705A>C (p.Asn902Thr) rs142823078 0.00026
NM_017433.5(MYO3A):c.1052A>C (p.Glu351Ala) rs141612979 0.00024
NM_017433.5(MYO3A):c.4840C>T (p.Gln1614Ter) rs146106052 0.00022
NM_017433.5(MYO3A):c.1796G>T (p.Ser599Ile) rs142289318 0.00019
NM_017433.5(MYO3A):c.656C>T (p.Thr219Met) rs377660409 0.00017
NM_017433.5(MYO3A):c.1207A>G (p.Ser403Gly) rs375646552 0.00014
NM_017433.5(MYO3A):c.1525T>C (p.Tyr509His) rs150793986 0.00011
NM_017433.5(MYO3A):c.2918G>A (p.Arg973Gln) rs142974032 0.00007
NM_017433.5(MYO3A):c.2803A>C (p.Met935Leu) rs375958934 0.00006
NM_017433.5(MYO3A):c.3007C>T (p.Leu1003Phe) rs776675167 0.00006
NM_017433.5(MYO3A):c.230A>C (p.Asn77Thr) rs1232229010 0.00005
NM_017433.5(MYO3A):c.3086A>G (p.Asp1029Gly) rs374226960 0.00004
NM_017433.5(MYO3A):c.4094A>C (p.Gln1365Pro) rs528252728 0.00004
NM_017433.5(MYO3A):c.743C>G (p.Pro248Arg) rs780657075 0.00004
NM_017433.5(MYO3A):c.2115-10A>G rs200205050 0.00003
NM_017433.5(MYO3A):c.2719G>A (p.Asp907Asn) rs727503325 0.00003
NM_017433.5(MYO3A):c.568T>C (p.Phe190Leu) rs727504671 0.00003
NM_017433.5(MYO3A):c.823C>T (p.Arg275Cys) rs755478240 0.00003
NM_017433.5(MYO3A):c.168C>T (p.His56=) rs201668920 0.00002
NM_017433.5(MYO3A):c.2849G>A (p.Arg950His) rs143371522 0.00002
NM_017433.5(MYO3A):c.3747T>A (p.Asn1249Lys) rs201263014 0.00002
NM_017433.5(MYO3A):c.4438+4A>G rs756581092 0.00002
NM_017433.5(MYO3A):c.1A>G (p.Met1Val) rs727504593 0.00001
NM_017433.5(MYO3A):c.2168A>G (p.Asn723Ser) rs771154512 0.00001
NM_017433.5(MYO3A):c.285G>T (p.Lys95Asn) rs1282051090 0.00001
NM_017433.5(MYO3A):c.4474C>A (p.Pro1492Thr) rs368473860 0.00001
NM_017433.5(MYO3A):c.1359+1G>T rs756836048
NM_017433.5(MYO3A):c.1643C>T (p.Pro548Leu) rs143918373
NM_017433.5(MYO3A):c.168+3_168+4del rs2130551945
NM_017433.5(MYO3A):c.1716C>A (p.Phe572Leu) rs751693978
NM_017433.5(MYO3A):c.2039A>C (p.Lys680Thr) rs1589000062
NM_017433.5(MYO3A):c.2405A>G (p.Gln802Arg) rs727503324
NM_017433.5(MYO3A):c.2890G>A (p.Asp964Asn) rs1554836048
NM_017433.5(MYO3A):c.3040A>G (p.Met1014Val) rs1324018685
NM_017433.5(MYO3A):c.3253A>G (p.Ser1085Gly) rs1191332923
NM_017433.5(MYO3A):c.4567C>G (p.Arg1523Gly) rs727504688
NM_017433.5(MYO3A):c.585+3C>T rs200381660
NM_017433.5(MYO3A):c.731+4A>T rs1184463802
NM_017433.5(MYO3A):c.731+4_731+5insTA rs727505119

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