ClinVar Miner

List of variants in gene MYO7A reported as benign for not provided

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Gene type:
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Total variants: 116
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HGVS dbSNP
GRCh37/hg19 11q13.5(chr11:76895772-76906312)x1
NM_000260.4(MYO7A):c.1003+298C>G rs4944144
NM_000260.4(MYO7A):c.1004-32T>C rs782322410
NM_000260.4(MYO7A):c.1004-35C>G rs2071151
NM_000260.4(MYO7A):c.1080+65T>C rs4944145
NM_000260.4(MYO7A):c.1299C>T (p.Ile433=) rs782163200
NM_000260.4(MYO7A):c.133-7C>T rs111033221
NM_000260.4(MYO7A):c.1343+253C>G rs11605022
NM_000260.4(MYO7A):c.1554+244T>C rs3740763
NM_000260.4(MYO7A):c.1554+8G>A rs111033227
NM_000260.4(MYO7A):c.1605C>T (p.Asn535=) rs111033228
NM_000260.4(MYO7A):c.1690+262A>G rs7937262
NM_000260.4(MYO7A):c.1691-126_1691-125insT rs11374303
NM_000260.4(MYO7A):c.1797+283T>C rs10736813
NM_000260.4(MYO7A):c.1854G>A (p.Leu618=) rs35429535
NM_000260.4(MYO7A):c.1935+191A>T rs948968
NM_000260.4(MYO7A):c.1936-23G>A rs2276283
NM_000260.4(MYO7A):c.2035G>A (p.Val679Ile) rs35641839
NM_000260.4(MYO7A):c.2106C>T (p.Arg702=) rs369787754
NM_000260.4(MYO7A):c.2181T>C (p.Phe727=) rs373656667
NM_000260.4(MYO7A):c.2187+208G>A rs11237106
NM_000260.4(MYO7A):c.2236G>A (p.Asp746Asn) rs36090425
NM_000260.4(MYO7A):c.2367+225T>C rs12577334
NM_000260.4(MYO7A):c.2367+269A>G rs10899356
NM_000260.4(MYO7A):c.2367+67T>C rs10793239
NM_000260.4(MYO7A):c.2447G>A (p.Arg816His) rs148343670
NM_000260.4(MYO7A):c.2694+134A>G rs1109162
NM_000260.4(MYO7A):c.2694+58G>A rs1109163
NM_000260.4(MYO7A):c.2695-58C>G rs3740762
NM_000260.4(MYO7A):c.2754C>T (p.Ala918=) rs78072361
NM_000260.4(MYO7A):c.286-5C>T rs111033471
NM_000260.4(MYO7A):c.288G>A (p.Thr96=) rs56023295
NM_000260.4(MYO7A):c.2905-54A>G rs7117606
NM_000260.4(MYO7A):c.3042G>T (p.Thr1014=) rs111033507
NM_000260.4(MYO7A):c.3109-68G>A rs2276287
NM_000260.4(MYO7A):c.3246G>A (p.Thr1082=) rs35963362
NM_000260.4(MYO7A):c.324C>T (p.Tyr108=) rs116892396
NM_000260.4(MYO7A):c.3375+33G>C rs948972
NM_000260.4(MYO7A):c.3404C>A (p.Ser1135Tyr) rs376688581
NM_000260.4(MYO7A):c.3474C>T (p.Ile1158=) rs201834743
NM_000260.4(MYO7A):c.3503+17G>A rs369969967
NM_000260.4(MYO7A):c.3504-122G>A rs12792197
NM_000260.4(MYO7A):c.3504-311G>A rs2186659
NM_000260.4(MYO7A):c.3750+89C>T rs2276286
NM_000260.4(MYO7A):c.3750+9G>A rs111033252
NM_000260.4(MYO7A):c.3751-119_3751-118insGCTGGGGCCTGGAGC rs55637648
NM_000260.4(MYO7A):c.3751-94C>G rs7947922
NM_000260.4(MYO7A):c.3828G>A (p.Ser1276=) rs78871677
NM_000260.4(MYO7A):c.3864C>T (p.Ala1288=) rs144657938
NM_000260.4(MYO7A):c.3924+109G>A rs4944148
NM_000260.4(MYO7A):c.3925-169C>T rs7952285
NM_000260.4(MYO7A):c.3925-243A>G rs7938356
NM_000260.4(MYO7A):c.3925-93C>G rs1944034
NM_000260.4(MYO7A):c.4023C>T (p.Pro1341=) rs73495790
NM_000260.4(MYO7A):c.4074C>T (p.Ser1358=) rs78996818
NM_000260.4(MYO7A):c.4323+156C>T rs948958
NM_000260.4(MYO7A):c.4323+35G>T rs1109977
NM_000260.4(MYO7A):c.4324-202A>G rs12421897
NM_000260.4(MYO7A):c.4324-207C>G rs12802853
NM_000260.4(MYO7A):c.4441+333C>A rs4945158
NM_000260.4(MYO7A):c.4441+7C>T rs372493678
NM_000260.4(MYO7A):c.4442-113A>G rs3781692
NM_000260.4(MYO7A):c.4442-7G>A rs372023062
NM_000260.4(MYO7A):c.4461C>T (p.Asn1487=) rs56174006
NM_000260.4(MYO7A):c.448C>A (p.Arg150=) rs121965079
NM_000260.4(MYO7A):c.4569-261C>T rs3781691
NM_000260.4(MYO7A):c.4589C>T (p.Ser1530Leu) rs111033183
NM_000260.4(MYO7A):c.4620G>A (p.Ala1540=) rs41298745
NM_000260.4(MYO7A):c.4668G>A (p.Pro1556=) rs376892582
NM_000260.4(MYO7A):c.468C>T (p.Ile156=) rs12420129
NM_000260.4(MYO7A):c.4697C>T (p.Thr1566Met) rs41298747
NM_000260.4(MYO7A):c.4698G>A (p.Thr1566=) rs200207753
NM_000260.4(MYO7A):c.470+96C>T rs55880704
NM_000260.4(MYO7A):c.4805G>A (p.Arg1602Gln) rs139889944
NM_000260.4(MYO7A):c.4845C>A (p.Pro1615=) rs61900036
NM_000260.4(MYO7A):c.486C>T (p.Ala162=) rs367687624
NM_000260.4(MYO7A):c.4950C>T (p.Asn1650=) rs80033599
NM_000260.4(MYO7A):c.4992C>T (p.Thr1664=) rs181573957
NM_000260.4(MYO7A):c.5005G>A (p.Val1669Ile) rs374655803
NM_000260.4(MYO7A):c.5044-247T>C rs11237118
NM_000260.4(MYO7A):c.510G>A (p.Leu170=) rs34477144
NM_000260.4(MYO7A):c.514C>T (p.Leu172=) rs368246776
NM_000260.4(MYO7A):c.5156A>G (p.Tyr1719Cys) rs77625410
NM_000260.4(MYO7A):c.5172C>G (p.Pro1724=) rs727505004
NM_000260.4(MYO7A):c.5215C>A (p.Arg1739=) rs111033477
NM_000260.4(MYO7A):c.5480+162C>G rs11237120
NM_000260.4(MYO7A):c.5481-83A>G rs11237121
NM_000260.4(MYO7A):c.5559C>T (p.His1853=) rs373612656
NM_000260.4(MYO7A):c.5598C>A (p.Leu1866=) rs111033504
NM_000260.4(MYO7A):c.5598C>T (p.Leu1866=) rs111033504
NM_000260.4(MYO7A):c.5637-175A>G rs4945160
NM_000260.4(MYO7A):c.5743-262G>C rs3819171
NM_000260.4(MYO7A):c.5835C>T (p.Leu1945=) rs111033476
NM_000260.4(MYO7A):c.5856+50G>A rs2276290
NM_000260.4(MYO7A):c.5866G>A (p.Val1956Ile) rs142293185
NM_000260.4(MYO7A):c.5904C>T (p.His1968=) rs41298753
NM_000260.4(MYO7A):c.593-5C>T rs762666
NM_000260.4(MYO7A):c.5944+57G>A rs948961
NM_000260.4(MYO7A):c.5944+67C>T rs948960
NM_000260.4(MYO7A):c.6051+155T>C rs11237122
NM_000260.4(MYO7A):c.6051+190T>G rs885442
NM_000260.4(MYO7A):c.6051+234C>G rs885441
NM_000260.4(MYO7A):c.6051+263G>A rs885440
NM_000260.4(MYO7A):c.6063G>A (p.Lys2021=) rs111033209
NM_000260.4(MYO7A):c.6240C>T (p.Ser2080=) rs41298757
NM_000260.4(MYO7A):c.639C>T (p.Phe213=) rs540197003
NM_000260.4(MYO7A):c.6438+50A>T rs2276289
NM_000260.4(MYO7A):c.6519C>T (p.Asn2173=) rs111033230
NM_000260.4(MYO7A):c.6558+51G>T rs948959
NM_000260.4(MYO7A):c.6559-257T>C rs869707
NM_000260.4(MYO7A):c.6614_6634dup (p.Met2205_Ser2211dup) rs111033388
NM_000260.4(MYO7A):c.6640G>A (p.Gly2214Ser) rs111033231
NM_000260.4(MYO7A):c.736-15_736-4dup rs111033503
NM_000260.4(MYO7A):c.736-47C>A rs3737454
NM_000260.4(MYO7A):c.905G>A (p.Arg302His) rs41298135
NM_000260.4(MYO7A):c.93C>T (p.Cys31=) rs35689081

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