ClinVar Miner

List of variants in gene MYO7A reported as uncertain significance by GeneDx

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Total variants: 20
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HGVS dbSNP
NM_000260.4(MYO7A):c.1871C>A (p.Thr624Lys) rs953533173
NM_000260.4(MYO7A):c.1960C>T (p.Arg654Cys) rs201928014
NM_000260.4(MYO7A):c.2002C>T (p.Arg668Cys) rs397516292
NM_000260.4(MYO7A):c.2527G>A (p.Val843Met) rs140559111
NM_000260.4(MYO7A):c.2558G>T (p.Arg853Leu) rs111033437
NM_000260.4(MYO7A):c.3750+5G>A rs111033391
NM_000260.4(MYO7A):c.388A>G (p.Met130Val) rs782473441
NM_000260.4(MYO7A):c.4018G>A (p.Ala1340Thr) rs376291076
NM_000260.4(MYO7A):c.4757A>G (p.Asn1586Ser) rs201251963
NM_000260.4(MYO7A):c.4916C>T (p.Thr1639Met) rs200848641
NM_000260.4(MYO7A):c.5166C>T (p.Phe1722=) rs566614598
NM_000260.4(MYO7A):c.5197G>A (p.Val1733Ile) rs1555103433
NM_000260.4(MYO7A):c.54G>C (p.Gln18His) rs371849195
NM_000260.4(MYO7A):c.5536C>G (p.Pro1846Ala) rs763456971
NM_000260.4(MYO7A):c.6002C>T (p.Thr2001Met) rs532542968
NM_000260.4(MYO7A):c.6236G>A (p.Arg2079Gln) rs765083332
NM_000260.4(MYO7A):c.6509C>T (p.Thr2170Ile) rs544709413
NM_000260.4(MYO7A):c.676G>A (p.Ala226Thr) rs201753022
NM_000260.4(MYO7A):c.910G>A (p.Ala304Thr) rs782124327
NM_000260.4(MYO7A):c.977T>A (p.Leu326Gln) rs797044491

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