ClinVar Miner

List of variants in gene MYH3 reported by CeGaT Center for Human Genetics Tuebingen

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Total variants: 33
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HGVS dbSNP gnomAD frequency
NM_002470.4(MYH3):c.3592G>A (p.Ala1198Thr) rs61735358 0.00641
NM_002470.4(MYH3):c.690C>G (p.Ala230=) rs147148934 0.00421
NM_002470.4(MYH3):c.4910C>T (p.Ala1637Val) rs34165480 0.00311
NM_002470.4(MYH3):c.2926-8C>T rs188588330 0.00296
NM_002470.4(MYH3):c.3594G>A (p.Ala1198=) rs139978727 0.00252
NM_002470.4(MYH3):c.3409C>T (p.Arg1137Cys) rs12941197 0.00245
NM_002470.4(MYH3):c.2289+4A>G rs111835858 0.00218
NM_002470.4(MYH3):c.5067G>T (p.Leu1689=) rs112858125 0.00205
NM_002470.4(MYH3):c.1932C>T (p.Ser644=) rs115612890 0.00194
NM_002470.4(MYH3):c.252G>A (p.Lys84=) rs147410236 0.00156
NM_002470.4(MYH3):c.3479C>T (p.Thr1160Met) rs145080512 0.00137
NM_002470.4(MYH3):c.-9+1G>A rs557849165 0.00117
NM_002470.4(MYH3):c.736-6A>G rs372079063 0.00067
NM_002470.4(MYH3):c.4647+6T>G rs375163919 0.00054
NM_002470.4(MYH3):c.5160+3G>A rs199942147 0.00017
NM_002470.4(MYH3):c.4752C>T (p.Ile1584=) rs189005323 0.00003
NM_002470.4(MYH3):c.3638G>A (p.Arg1213Gln) rs773055884 0.00001
NM_002470.4(MYH3):c.4801G>A (p.Ala1601Thr) rs764578014 0.00001
NM_002470.4(MYH3):c.5528A>G (p.Lys1843Arg) rs1180621599 0.00001
NM_002470.4(MYH3):c.1064G>A (p.Gly355Glu) rs1597489612
NM_002470.4(MYH3):c.1838C>T (p.Ser613Phe) rs2074282243
NM_002470.4(MYH3):c.2306G>A (p.Gly769Asp) rs2142400622
NM_002470.4(MYH3):c.2395C>T (p.Arg799Cys) rs146342659
NM_002470.4(MYH3):c.3062T>C (p.Leu1021Ser)
NM_002470.4(MYH3):c.3558C>T (p.His1186=) rs199527777
NM_002470.4(MYH3):c.3767A>C (p.Gln1256Pro)
NM_002470.4(MYH3):c.38C>T (p.Ala13Val)
NM_002470.4(MYH3):c.4018G>A (p.Asp1340Asn)
NM_002470.4(MYH3):c.4133C>T (p.Thr1378Met)
NM_002470.4(MYH3):c.4313C>T (p.Ser1438Phe) rs1447420349
NM_002470.4(MYH3):c.5254G>A (p.Ala1752Thr) rs34393601
NM_002470.4(MYH3):c.5695A>G (p.Lys1899Glu)
NM_002470.4(MYH3):c.82C>T (p.Gln28Ter) rs2142431278

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