ClinVar Miner

List of variants in gene MYO15A studied for Hearing impairment

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Total variants: 20
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HGVS dbSNP gnomAD frequency
NM_016239.4(MYO15A):c.7984C>G (p.Leu2662Val) rs200930743 0.00058
NM_016239.4(MYO15A):c.10181C>T (p.Ala3394Val) rs200249886 0.00024
NM_016239.4(MYO15A):c.8183G>A (p.Arg2728His) rs184435771 0.00011
NM_016239.4(MYO15A):c.8281G>A (p.Val2761Met) rs367717396 0.00004
NM_016239.4(MYO15A):c.9515A>G (p.Gln3172Arg) rs375465287 0.00002
NM_016239.4(MYO15A):c.2677C>T (p.Arg893Ter) rs763075073 0.00001
NM_016239.4(MYO15A):c.3646C>T (p.Arg1216Cys) rs547573001 0.00001
NM_016239.4(MYO15A):c.4039A>T (p.Ile1347Phe) rs375627187 0.00001
NM_016239.4(MYO15A):c.4351G>A (p.Asp1451Asn) rs767270134 0.00001
NM_016239.4(MYO15A):c.5491G>A (p.Gly1831Arg) rs1260018632 0.00001
NM_016239.3(MYO15A):c.419dup (p.Phe141Valfs) rs750130520
NM_016239.4(MYO15A):c.1137del (p.Tyr380fs) rs769260536
NM_016239.4(MYO15A):c.1238G>C (p.Trp413Ser) rs2142245203
NM_016239.4(MYO15A):c.266A>C (p.Gln89Pro) rs2142237084
NM_016239.4(MYO15A):c.2873del (p.Pro958fs) rs1217492313
NM_016239.4(MYO15A):c.4240G>A (p.Glu1414Lys) rs1060499798
NM_016239.4(MYO15A):c.8261C>T (p.Thr2754Met) rs766544188
NM_016239.4(MYO15A):c.9467T>C (p.Leu3156Pro) rs2046774616
NM_016239.4(MYO15A):c.9583C>T (p.Pro3195Ser) rs2142402540
NM_016239.4(MYO15A):c.9620G>T (p.Arg3207Leu) rs199621031

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