ClinVar Miner

List of variants in gene MYO15A reported as pathogenic for auditory system disease

Included ClinVar conditions (549):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 79
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HGVS dbSNP
NC_000017.1:g.18054799_18058246delinsCTCCCCGGAACGGCTGCTGGTAC
NM_016239.3(MYO15A):c.419dup (p.Phe141Valfs) rs750130520
NM_016239.3(MYO15A):c.8183G>A rs184435771
NM_016239.3(MYO15A):c.[373_374delCG];[8183G>A]
NM_016239.4(MYO15A):c.10572dup (p.Ser3525fs) rs1057519607
NM_016239.4(MYO15A):c.10573del (p.Ser3525fs) rs1270302810
NM_016239.4(MYO15A):c.10585del (p.Leu3529fs)
NM_016239.4(MYO15A):c.1137del (p.Tyr380fs) rs769260536
NM_016239.4(MYO15A):c.1171_1177dup (p.Tyr393fs) rs1567620939
NM_016239.4(MYO15A):c.1185dup (p.Glu396fs) rs772536599
NM_016239.4(MYO15A):c.1223C>T (p.Ala408Val) rs191710555
NM_016239.4(MYO15A):c.1615C>T (p.Gln539Ter) rs1597752877
NM_016239.4(MYO15A):c.3311dup (p.Gly1104_Glu1105insTer) rs794729637
NM_016239.4(MYO15A):c.3313G>T (p.Glu1105Ter) rs121908971
NM_016239.4(MYO15A):c.3336del (p.Arg1113fs) rs769884586
NM_016239.4(MYO15A):c.3505C>T (p.Arg1169Ter) rs781546107
NM_016239.4(MYO15A):c.3524dup (p.Ser1176fs) rs766187994
NM_016239.4(MYO15A):c.3685C>T (p.Gln1229Ter) rs121908968
NM_016239.4(MYO15A):c.3756+1G>T rs748108031
NM_016239.4(MYO15A):c.3944G>A (p.Gly1315Glu) rs878854410
NM_016239.4(MYO15A):c.4108C>T (p.Arg1370Cys) rs878854411
NM_016239.4(MYO15A):c.4198G>A (p.Val1400Met) rs749136456
NM_016239.4(MYO15A):c.4240G>A (p.Glu1414Lys) rs1060499798
NM_016239.4(MYO15A):c.4351G>A (p.Asp1451Asn)
NM_016239.4(MYO15A):c.4522G>T (p.Glu1508Ter) rs1567638693
NM_016239.4(MYO15A):c.4528C>T (p.Gln1510Ter) rs779077039
NM_016239.4(MYO15A):c.4570C>T (p.Gln1524Ter) rs1209665716
NM_016239.4(MYO15A):c.4571dup (p.Lys1525fs)
NM_016239.4(MYO15A):c.4609G>T (p.Glu1537Ter) rs1555543432
NM_016239.4(MYO15A):c.4642G>A (p.Ala1548Thr) rs201067821
NM_016239.4(MYO15A):c.477G>A (p.Trp159Ter) rs1567618790
NM_016239.4(MYO15A):c.4780G>C (p.Asp1594His) rs878854412
NM_016239.4(MYO15A):c.4879G>T (p.Glu1627Ter) rs1597787868
NM_016239.4(MYO15A):c.488C>A (p.Ser163Ter) rs773729617
NM_016239.4(MYO15A):c.5005C>T (p.Gln1669Ter) rs1567641234
NM_016239.4(MYO15A):c.5335del (p.Leu1779fs) rs878854413
NM_016239.4(MYO15A):c.5492G>T (p.Gly1831Val) rs121908972
NM_016239.4(MYO15A):c.5531+1G>A rs727503309
NM_016239.4(MYO15A):c.5673C>G (p.Tyr1891Ter)
NM_016239.4(MYO15A):c.5809C>T (p.Arg1937Cys) rs749465098
NM_016239.4(MYO15A):c.5851del (p.Ser1951fs) rs727504995
NM_016239.4(MYO15A):c.5896C>T (p.Arg1966Ter) rs765468034
NM_016239.4(MYO15A):c.5925G>A (p.Trp1975Ter) rs375290498
NM_016239.4(MYO15A):c.5964+3G>C rs530975087
NM_016239.4(MYO15A):c.605C>A (p.Pro202His) rs1229200252
NM_016239.4(MYO15A):c.6146C>A (p.Pro2049His) rs878854414
NM_016239.4(MYO15A):c.6178-2A>G rs878854415
NM_016239.4(MYO15A):c.625G>T (p.Glu209Ter) rs571594379
NM_016239.4(MYO15A):c.6331A>T (p.Asn2111Tyr) rs121908966
NM_016239.4(MYO15A):c.6337A>T (p.Ile2113Phe) rs121908965
NM_016239.4(MYO15A):c.6340G>A (p.Val2114Met) rs377385081
NM_016239.4(MYO15A):c.6503T>G (p.Leu2168Arg) rs1567648703
NM_016239.4(MYO15A):c.6589C>T (p.Gln2197Ter) rs779445819
NM_016239.4(MYO15A):c.6638G>A (p.Trp2213Ter) rs1567649945
NM_016239.4(MYO15A):c.6944del (p.Gly2315fs) rs1057519604
NM_016239.4(MYO15A):c.7006C>T (p.Gln2336Ter)
NM_016239.4(MYO15A):c.7124_7127del (p.Asp2375fs) rs780170125
NM_016239.4(MYO15A):c.7207G>T (p.Asp2403Tyr) rs878853227
NM_016239.4(MYO15A):c.742C>G (p.Arg248Gly) rs878854409
NM_016239.4(MYO15A):c.7745_8224+177delinsCTCCCCGGAACGGCTGCTGGTAC
NM_016239.4(MYO15A):c.7801A>T (p.Lys2601Ter) rs121908967
NM_016239.4(MYO15A):c.8005dup (p.Thr2669fs) rs1221876133
NM_016239.4(MYO15A):c.8050T>C (p.Tyr2684His) rs376351191
NM_016239.4(MYO15A):c.8090T>C (p.Val2697Ala) rs200451098
NM_016239.4(MYO15A):c.8148G>T (p.Gln2716His) rs121908969
NM_016239.4(MYO15A):c.8340G>A (p.Thr2780=) rs878853228
NM_016239.4(MYO15A):c.8375T>C (p.Val2792Ala)
NM_016239.4(MYO15A):c.8467G>A (p.Asp2823Asn) rs878853238
NM_016239.4(MYO15A):c.8524G>T (p.Glu2842Ter) rs766250454
NM_016239.4(MYO15A):c.8714-1G>A rs377015931
NM_016239.4(MYO15A):c.8897_8900dup (p.Ala2968fs)
NM_016239.4(MYO15A):c.8968-1G>C rs746051220
NM_016239.4(MYO15A):c.9083+6T>A rs1555547112
NM_016239.4(MYO15A):c.9229+2T>C rs1057519606
NM_016239.4(MYO15A):c.9572G>A (p.Arg3191His) rs373520843
NM_016239.4(MYO15A):c.9861C>T (p.Gly3287=) rs372466080
NM_016239.4(MYO15A):c.9958_9961del (p.Asp3320fs) rs1567664131
NM_016239.4(MYO15A):c.996C>G (p.Tyr332Ter) rs759523751
NM_016239.4(MYO15A):c.[1185dup];[4879G>T]

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