ClinVar Miner

List of variants in gene MYH14 reported as uncertain significance for not specified

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Total variants: 57
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HGVS dbSNP
NM_001145809.1(MYH14):c.1095C>A (p.Phe365Leu) rs727505251
NM_001145809.1(MYH14):c.1174C>T (p.Arg392Trp) rs778312429
NM_001145809.1(MYH14):c.1265C>G (p.Ala422Gly) rs372324948
NM_001145809.1(MYH14):c.1381C>T (p.Arg461Cys) rs752732851
NM_001145809.1(MYH14):c.1382G>A (p.Arg461His) rs370353590
NM_001145809.1(MYH14):c.1655C>T (p.Pro552Leu) rs727505282
NM_001145809.1(MYH14):c.1918C>T (p.Arg640Trp) rs376267080
NM_001145809.1(MYH14):c.1919G>A (p.Arg640Gln) rs199696801
NM_001145809.1(MYH14):c.2458C>T (p.Arg820Cys) rs767984672
NM_001145809.1(MYH14):c.2667C>G (p.His889Gln) rs876657872
NM_001145809.1(MYH14):c.2839C>T (p.Arg947Cys) rs757658628
NM_001145809.1(MYH14):c.2840G>A (p.Arg947His) rs374883445
NM_001145809.1(MYH14):c.2900C>G (p.Thr967Arg) rs142134135
NM_001145809.1(MYH14):c.3304C>T (p.Arg1102Trp) rs397516629
NM_001145809.1(MYH14):c.3322C>T (p.Arg1108Cys) rs769702697
NM_001145809.1(MYH14):c.3433C>T (p.Arg1145Trp) rs773117828
NM_001145809.1(MYH14):c.3467+1G>A rs727503223
NM_001145809.1(MYH14):c.3475G>T (p.Asp1159Tyr) rs370256265
NM_001145809.1(MYH14):c.3571G>T (p.Ala1191Ser) rs776570317
NM_001145809.1(MYH14):c.3623C>T (p.Ala1208Val) rs758560911
NM_001145809.1(MYH14):c.3914G>A (p.Arg1305His) rs876657873
NM_001145809.1(MYH14):c.4088G>A (p.Arg1363His) rs727504915
NM_001145809.1(MYH14):c.4259C>T (p.Ala1420Val) rs727503225
NM_001145809.1(MYH14):c.4264C>T (p.Arg1422Cys) rs727503226
NM_001145809.1(MYH14):c.4297G>A (p.Glu1433Lys) rs771755654
NM_001145809.1(MYH14):c.4307G>A (p.Arg1436Gln) rs773527189
NM_001145809.1(MYH14):c.4370G>A (p.Arg1457Gln) rs727503224
NM_001145809.1(MYH14):c.4393C>T (p.Arg1465Cys) rs727505272
NM_001145809.1(MYH14):c.4439G>A (p.Arg1480His) rs187782753
NM_001145809.1(MYH14):c.4441C>T (p.Arg1481Cys) rs727503227
NM_001145809.1(MYH14):c.4486C>G (p.Gln1496Glu) rs141995460
NM_001145809.1(MYH14):c.4694G>A (p.Arg1565Gln) rs374911327
NM_001145809.1(MYH14):c.4705G>T (p.Ala1569Ser) rs145522874
NM_001145809.1(MYH14):c.4921C>T (p.Arg1641Cys) rs748898201
NM_001145809.1(MYH14):c.5271G>A (p.Ser1757=) rs397516630
NM_001145809.1(MYH14):c.5345+6T>C rs876657874
NM_001145809.1(MYH14):c.5369G>A (p.Arg1790His) rs747480201
NM_001145809.1(MYH14):c.5446C>T (p.Arg1816Cys) rs376798395
NM_001145809.1(MYH14):c.5530G>A (p.Gly1844Arg) rs375748088
NM_001145809.1(MYH14):c.5548C>T (p.Arg1850Trp) rs201474958
NM_001145809.1(MYH14):c.563-3C>G rs1555755418
NM_001145809.1(MYH14):c.5644G>A (p.Ala1882Thr) rs200566974
NM_001145809.1(MYH14):c.5683C>T (p.Arg1895Cys) rs200485394
NM_001145809.1(MYH14):c.5876G>A (p.Arg1959Gln) rs200878464
NM_001145809.1(MYH14):c.5959C>T (p.Arg1987Ter) rs727503230
NM_001145809.1(MYH14):c.5960+4T>C rs1555779636
NM_001145809.1(MYH14):c.5975C>T (p.Thr1992Ile) rs1555779737
NM_001145809.1(MYH14):c.6088T>A (p.Ser2030Thr) rs727503231
NM_001145809.1(MYH14):c.693C>T (p.Pro231=) rs373744231
NM_001145809.1(MYH14):c.949G>A (p.Gly317Arg) rs727503222
NM_024729.3(MYH14):c.2236G>A (p.Glu746Lys) rs397516628
NM_024729.3(MYH14):c.2975C>T (p.Thr992Met) rs201746408
NM_024729.3(MYH14):c.526G>A (p.Ala176Thr) rs138001307
NM_024729.3(MYH14):c.5476C>T (p.Arg1826Cys) rs187789045
NM_024729.3(MYH14):c.565C>T (p.Arg189Cys) rs200818171
NM_024729.3(MYH14):c.5867C>T (p.Thr1956Met) rs201986144
NM_024729.3(MYH14):c.796A>G (p.Ile266Val) rs200424400

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