ClinVar Miner

List of variants in gene MYO7A reported as uncertain significance by Illumina Clinical Services Laboratory,Illumina

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Gene type:
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Total variants: 81
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HGVS dbSNP
NM_000260.3(MYO7A):c.*101G>A rs886048683
NM_000260.3(MYO7A):c.*142A>G rs369873505
NM_000260.3(MYO7A):c.*208C>G rs886048684
NM_000260.3(MYO7A):c.-154G>A rs545774605
NM_000260.3(MYO7A):c.-160G>A rs576789908
NM_000260.3(MYO7A):c.-170C>T rs886048667
NM_000260.3(MYO7A):c.-196C>T rs886048666
NM_000260.3(MYO7A):c.-20G>A rs886048668
NM_000260.3(MYO7A):c.-211A>G rs41298129
NM_000260.3(MYO7A):c.1242C>T (p.Ile414=) rs886048673
NM_000260.3(MYO7A):c.1288C>T (p.Arg430Cys) rs201839693
NM_000260.3(MYO7A):c.1344-7C>G rs886048674
NM_000260.3(MYO7A):c.1358G>A (p.Cys453Tyr) rs202080237
NM_000260.3(MYO7A):c.1554+7C>T rs150114658
NM_000260.3(MYO7A):c.1554G>A (p.Lys518=) rs886048675
NM_000260.3(MYO7A):c.156C>G (p.Asn52Lys) rs886048669
NM_000260.3(MYO7A):c.160A>G (p.Thr54Ala) rs369142107
NM_000260.3(MYO7A):c.1619C>A (p.Pro540His) rs782607566
NM_000260.3(MYO7A):c.1690+9G>T rs371146074
NM_000260.3(MYO7A):c.1801G>A (p.Ala601Thr) rs782481491
NM_000260.3(MYO7A):c.186G>A (p.Thr62=) rs368267301
NM_000260.3(MYO7A):c.2057G>A (p.Arg686His) rs781991817
NM_000260.3(MYO7A):c.2107G>A (p.Gly703Arg) rs572300575
NM_000260.3(MYO7A):c.2146C>G (p.His716Asp) rs886048676
NM_000260.3(MYO7A):c.215G>T (p.Arg72Leu) rs886048670
NM_000260.3(MYO7A):c.225C>A (p.Asp75Glu) rs782757893
NM_000260.3(MYO7A):c.2283G>A (p.Arg761=) rs111033229
NM_000260.3(MYO7A):c.2293C>A (p.Leu765Met) rs201203036
NM_000260.3(MYO7A):c.2372G>A (p.Arg791His) rs782693893
NM_000260.3(MYO7A):c.239G>A (p.Gly80Asp) rs376796087
NM_000260.3(MYO7A):c.2411G>A (p.Arg804Gln) rs561347333
NM_000260.3(MYO7A):c.2489G>A (p.Arg830His) rs371029653
NM_000260.3(MYO7A):c.2507G>A (p.Arg836His) rs782179888
NM_000260.3(MYO7A):c.2527G>A (p.Val843Met) rs140559111
NM_000260.3(MYO7A):c.2618G>A (p.Arg873Gln) rs1052032
NM_000260.3(MYO7A):c.2679C>T (p.Ala893=) rs782279442
NM_000260.3(MYO7A):c.2697G>A (p.Glu899=) rs782531164
NM_000260.3(MYO7A):c.2759G>A (p.Arg920Gln) rs565162134
NM_000260.3(MYO7A):c.2882G>A (p.Gly961Asp) rs199575418
NM_000260.3(MYO7A):c.288G>T (p.Thr96=) rs56023295
NM_000260.3(MYO7A):c.3014C>T (p.Ala1005Val) rs113326082
NM_000260.3(MYO7A):c.3283G>A (p.Glu1095Lys) rs199810429
NM_000260.3(MYO7A):c.3375+3G>A rs397516299
NM_000260.3(MYO7A):c.3415G>A (p.Gly1139Ser) rs200840044
NM_000260.3(MYO7A):c.351G>T (p.Glu117Asp) rs886048671
NM_000260.3(MYO7A):c.3662C>G (p.Pro1221Arg) rs780594308
NM_000260.3(MYO7A):c.380T>C (p.Ile127Thr) rs41298131
NM_000260.3(MYO7A):c.3858G>A (p.Ala1286=) rs372623270
NM_000260.3(MYO7A):c.4039C>T (p.Arg1347Cys) rs111534474
NM_000260.3(MYO7A):c.4118G>A (p.Arg1373Gln) rs886048677
NM_000260.3(MYO7A):c.4280C>T (p.Thr1427Met) rs547006116
NM_000260.3(MYO7A):c.4450C>T (p.Leu1484Phe) rs200416912
NM_000260.3(MYO7A):c.4630G>A (p.Gly1544Ser) rs886048678
NM_000260.3(MYO7A):c.4842C>A (p.Asn1614Lys) rs749146420
NM_000260.3(MYO7A):c.4851C>T (p.Pro1617=) rs372535399
NM_000260.3(MYO7A):c.5037G>A (p.Glu1679=) rs886048679
NM_000260.3(MYO7A):c.5088G>T (p.Arg1696=) rs886048680
NM_000260.3(MYO7A):c.5108C>T (p.Ala1703Val) rs199561332
NM_000260.3(MYO7A):c.5172C>G (p.Pro1724=) rs727505004
NM_000260.3(MYO7A):c.5214C>A (p.Ala1738=) rs886048681
NM_000260.3(MYO7A):c.5265G>A (p.Ala1755=) rs773557376
NM_000260.3(MYO7A):c.5380G>A (p.Glu1794Lys) rs762836180
NM_000260.3(MYO7A):c.549G>A (p.Ser183=) rs188198404
NM_000260.3(MYO7A):c.562C>G (p.Gln188Glu) rs572959359
NM_000260.3(MYO7A):c.5640C>T (p.Asn1880=) rs140664109
NM_000260.3(MYO7A):c.5661G>A (p.Pro1887=) rs375627342
NM_000260.3(MYO7A):c.5667G>C (p.Leu1889=) rs747516555
NM_000260.3(MYO7A):c.571G>C (p.Glu191Gln) rs886048672
NM_000260.3(MYO7A):c.5820A>G (p.Ser1940=) rs886048682
NM_000260.3(MYO7A):c.5851G>C (p.Asp1951His) rs767931313
NM_000260.3(MYO7A):c.5896G>A (p.Val1966Ile) rs371313080
NM_000260.3(MYO7A):c.5904C>T (p.His1968=) rs41298753
NM_000260.3(MYO7A):c.5930G>A (p.Arg1977Gln) rs762420918
NM_000260.3(MYO7A):c.5950G>A (p.Val1984Met) rs377517717
NM_000260.3(MYO7A):c.6247G>A (p.Ala2083Thr) rs41298759
NM_000260.3(MYO7A):c.6600G>C (p.Gln2200His) rs779431269
NM_000260.3(MYO7A):c.874C>T (p.Arg292Trp) rs782505601
NM_000260.3(MYO7A):c.895G>A (p.Ala299Thr) rs372344870
NM_000260.3(MYO7A):c.977T>A (p.Leu326Gln) rs797044491
NM_000260.4(MYO7A):c.2282+1G>C
NM_000260.4(MYO7A):c.4105C>T (p.Gln1369Ter)

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