ClinVar Miner

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

Included ClinVar conditions (549):
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Gene type:
ClinVar version:
Total variants: 112
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HGVS dbSNP
NM_017433.5(MYO3A):c.*195C>T
NM_017433.5(MYO3A):c.*233C>T rs569425203
NM_017433.5(MYO3A):c.*239C>T
NM_017433.5(MYO3A):c.*270A>G rs115859827
NM_017433.5(MYO3A):c.*2C>G rs768182699
NM_017433.5(MYO3A):c.*327G>A rs886046928
NM_017433.5(MYO3A):c.*354A>G
NM_017433.5(MYO3A):c.*422C>G rs886046930
NM_017433.5(MYO3A):c.*435G>T rs886046931
NM_017433.5(MYO3A):c.*476G>A
NM_017433.5(MYO3A):c.*493G>A rs72787376
NM_017433.5(MYO3A):c.*538G>T
NM_017433.5(MYO3A):c.-109C>T
NM_017433.5(MYO3A):c.-146G>A
NM_017433.5(MYO3A):c.-30A>G
NM_017433.5(MYO3A):c.-37A>G rs564519092
NM_017433.5(MYO3A):c.-50A>G rs886046917
NM_017433.5(MYO3A):c.1111G>A (p.Val371Met)
NM_017433.5(MYO3A):c.1170+15G>A rs764976663
NM_017433.5(MYO3A):c.1207A>G (p.Ser403Gly) rs375646552
NM_017433.5(MYO3A):c.1242A>T (p.Gly414=) rs3758442
NM_017433.5(MYO3A):c.1276-5T>C rs142877629
NM_017433.5(MYO3A):c.152T>A (p.Ile51Asn) rs144008984
NM_017433.5(MYO3A):c.1559C>T (p.Ala520Val) rs72787346
NM_017433.5(MYO3A):c.1561A>C (p.Ile521Leu)
NM_017433.5(MYO3A):c.1562T>C (p.Ile521Thr) rs886046921
NM_017433.5(MYO3A):c.1583T>C (p.Ile528Thr) rs886046922
NM_017433.5(MYO3A):c.1588dup (p.Tyr530fs) rs1564543838
NM_017433.5(MYO3A):c.1643C>A (p.Pro548His) rs143918373
NM_017433.5(MYO3A):c.1662-9T>A rs200678745
NM_017433.5(MYO3A):c.170A>C (p.Asp57Ala) rs146511800
NM_017433.5(MYO3A):c.1746A>G (p.Gln582=) rs775168365
NM_017433.5(MYO3A):c.1777-14G>T rs4592324
NM_017433.5(MYO3A):c.177C>T (p.Asp59=) rs139958275
NM_017433.5(MYO3A):c.1792T>C (p.Tyr598His) rs886046923
NM_017433.5(MYO3A):c.1828A>G (p.Ile610Val) rs151254539
NM_017433.5(MYO3A):c.1899G>T (p.Glu633Asp)
NM_017433.5(MYO3A):c.1971T>C (p.Thr657=) rs112195128
NM_017433.5(MYO3A):c.1975G>A (p.Gly659Arg)
NM_017433.5(MYO3A):c.1991G>T (p.Arg664Leu) rs886042194
NM_017433.5(MYO3A):c.2016C>T (p.Thr672=) rs56207573
NM_017433.5(MYO3A):c.2115-10A>G rs200205050
NM_017433.5(MYO3A):c.2115-7C>A rs764917474
NM_017433.5(MYO3A):c.2133G>A (p.Leu711=) rs56147819
NM_017433.5(MYO3A):c.2169T>C (p.Asn723=) rs114982270
NM_017433.5(MYO3A):c.2188G>A (p.Glu730Lys)
NM_017433.5(MYO3A):c.2263-3T>G rs750600802
NM_017433.5(MYO3A):c.2275A>T (p.Asn759Tyr) rs201033926
NM_017433.5(MYO3A):c.233T>G (p.Val78Gly)
NM_017433.5(MYO3A):c.2625G>C (p.Leu875=) rs371741845
NM_017433.5(MYO3A):c.2701A>G (p.Ile901Val) rs1371951424
NM_017433.5(MYO3A):c.2705A>C (p.Asn902Thr) rs142823078
NM_017433.5(MYO3A):c.2774C>T (p.Thr925Met) rs149803315
NM_017433.5(MYO3A):c.2854A>C (p.Ile952Leu) rs767552680
NM_017433.5(MYO3A):c.2870A>G (p.Glu957Gly) rs764192576
NM_017433.5(MYO3A):c.2973G>T (p.Arg991=) rs146647767
NM_017433.5(MYO3A):c.2999G>A (p.Arg1000Gln)
NM_017433.5(MYO3A):c.3000-11T>C rs375346333
NM_017433.5(MYO3A):c.3028G>A (p.Glu1010Lys) rs61729833
NM_017433.5(MYO3A):c.3035C>T (p.Pro1012Leu) rs146852484
NM_017433.5(MYO3A):c.3037C>T (p.Arg1013Cys) rs140154015
NM_017433.5(MYO3A):c.3085G>A (p.Asp1029Asn)
NM_017433.5(MYO3A):c.3133G>A (p.Val1045Met) rs35447806
NM_017433.5(MYO3A):c.3155G>A (p.Arg1052Gln) rs267602452
NM_017433.5(MYO3A):c.3255C>T (p.Ser1085=) rs35541310
NM_017433.5(MYO3A):c.3256G>A (p.Ala1086Thr) rs568909391
NM_017433.5(MYO3A):c.332T>C (p.Leu111Pro) rs886046918
NM_017433.5(MYO3A):c.3337G>A (p.Val1113Ile) rs770255390
NM_017433.5(MYO3A):c.3352A>G (p.Thr1118Ala) rs138955440
NM_017433.5(MYO3A):c.3398+3A>G rs373758358
NM_017433.5(MYO3A):c.3408C>T (p.Phe1136=) rs61731629
NM_017433.5(MYO3A):c.3537G>A (p.Val1179=) rs774297046
NM_017433.5(MYO3A):c.3538G>A (p.Glu1180Lys) rs184043065
NM_017433.5(MYO3A):c.3584T>C (p.Val1195Ala) rs35675577
NM_017433.5(MYO3A):c.3661C>G (p.Leu1221Val) rs886046924
NM_017433.5(MYO3A):c.3729G>A (p.Arg1243=) rs146832858
NM_017433.5(MYO3A):c.3730T>C (p.Tyr1244His) rs148993025
NM_017433.5(MYO3A):c.3757T>C (p.Ser1253Pro) rs541189709
NM_017433.5(MYO3A):c.3763G>A (p.Ala1255Thr)
NM_017433.5(MYO3A):c.3774A>T (p.Leu1258=)
NM_017433.5(MYO3A):c.3859C>A (p.Pro1287Thr) rs35575696
NM_017433.5(MYO3A):c.3862A>G (p.Thr1288Ala) rs886046925
NM_017433.5(MYO3A):c.3880A>G (p.Ile1294Val) rs56261037
NM_017433.5(MYO3A):c.3932C>G (p.Thr1311Ser) rs146693681
NM_017433.5(MYO3A):c.3993C>T (p.Val1331=) rs373422750
NM_017433.5(MYO3A):c.4140C>T (p.Val1380=)
NM_017433.5(MYO3A):c.4250C>T (p.Thr1417Ile) rs34151474
NM_017433.5(MYO3A):c.4407T>C (p.Asn1469=) rs199843655
NM_017433.5(MYO3A):c.4465A>G (p.Ile1489Val) rs147376000
NM_017433.5(MYO3A):c.4489C>T (p.Arg1497Trp) rs886046926
NM_017433.5(MYO3A):c.4505T>G (p.Leu1502Ter) rs754217606
NM_017433.5(MYO3A):c.4530C>T (p.Tyr1510=) rs139504940
NM_017433.5(MYO3A):c.4567C>G (p.Arg1523Gly) rs727504688
NM_017433.5(MYO3A):c.4589A>T (p.Gln1530Leu) rs147749053
NM_017433.5(MYO3A):c.4681C>T (p.Arg1561Ter) rs138593211
NM_017433.5(MYO3A):c.4730+11A>C rs375717548
NM_017433.5(MYO3A):c.4743G>A (p.Ala1581=) rs886046927
NM_017433.5(MYO3A):c.4840C>T (p.Gln1614Ter) rs146106052
NM_017433.5(MYO3A):c.4849T>C (p.Ter1617Gln) rs141985215
NM_017433.5(MYO3A):c.509-15T>C
NM_017433.5(MYO3A):c.546G>T (p.Arg182=) rs148349532
NM_017433.5(MYO3A):c.555del (p.Ser185_Val186insTer) rs773432148
NM_017433.5(MYO3A):c.610G>A (p.Asp204Asn) rs3737274
NM_017433.5(MYO3A):c.656C>T (p.Thr219Met) rs377660409
NM_017433.5(MYO3A):c.706A>G (p.Met236Val) rs766118638
NM_017433.5(MYO3A):c.848A>C (p.Gln283Pro) rs199541460
NM_017433.5(MYO3A):c.859A>C (p.Ile287Leu) rs886046919
NM_017433.5(MYO3A):c.906G>A (p.Thr302=) rs139818474
NM_017433.5(MYO3A):c.912C>A (p.Phe304Leu)
NM_017433.5(MYO3A):c.938G>A (p.Gly313Asp) rs527881627
NM_017433.5(MYO3A):c.949G>C (p.Ala317Pro) rs61731652
NM_017433.5(MYO3A):c.991C>T (p.Arg331Ter) rs749269594

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