ClinVar Miner

List of variants in gene MYH3 reported as uncertain significance for not specified

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Total variants: 13
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HGVS dbSNP gnomAD frequency
NM_002470.4(MYH3):c.875C>G (p.Ser292Cys) rs139480342 0.00068
NM_002470.4(MYH3):c.376G>C (p.Val126Leu) rs201787435 0.00029
NM_002470.4(MYH3):c.3976-3C>T rs200078403 0.00009
NM_002470.4(MYH3):c.2668C>G (p.Leu890Val) rs879255375 0.00001
NM_002470.4(MYH3):c.1480A>G (p.Met494Val) rs797045726
NM_002470.4(MYH3):c.1625C>G (p.Pro542Arg) rs1057518378
NM_002470.4(MYH3):c.1802C>T (p.Pro601Leu) rs797045728
NM_002470.4(MYH3):c.1960-5C>T
NM_002470.4(MYH3):c.2389C>T (p.Leu797Phe) rs1057518547
NM_002470.4(MYH3):c.3413G>A (p.Ser1138Asn)
NM_002470.4(MYH3):c.3611T>C (p.Leu1204Pro) rs1057518008
NM_002470.4(MYH3):c.52C>T (p.Arg18Trp)
NM_002470.4(MYH3):c.62A>G (p.Glu21Gly) rs1358980010

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