ClinVar Miner

List of variants in gene combination MHRT, MYH7 reported as uncertain significance for not specified

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Total variants: 55
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HGVS dbSNP
NM_000257.4(MYH7):c.4276G>A (p.Glu1426Lys) rs397516208
NM_000257.4(MYH7):c.4283T>C (p.Leu1428Ser) rs727503244
NM_000257.4(MYH7):c.4330A>G (p.Lys1444Glu) rs397516210
NM_000257.4(MYH7):c.4348G>A (p.Asp1450Asn) rs397516211
NM_000257.4(MYH7):c.4354-2A>C rs727504734
NM_000257.4(MYH7):c.4354-7C>T rs370093487
NM_000257.4(MYH7):c.4363G>A (p.Glu1455Lys) rs876661373
NM_000257.4(MYH7):c.4388C>T (p.Ser1463Leu) rs890401818
NM_000257.4(MYH7):c.4399C>G (p.Leu1467Val) rs397516214
NM_000257.4(MYH7):c.4402G>A (p.Glu1468Lys) rs876657884
NM_000257.4(MYH7):c.4402G>C (p.Glu1468Gln) rs876657884
NM_000257.4(MYH7):c.4408T>C (p.Ser1470Pro) rs397516215
NM_000257.4(MYH7):c.4411C>T (p.Gln1471Ter) rs397516216
NM_000257.4(MYH7):c.4423C>T (p.Arg1475Cys) rs139646545
NM_000257.4(MYH7):c.4436C>T (p.Thr1479Ile) rs397516217
NM_000257.4(MYH7):c.4470G>C (p.Glu1490Asp) rs730880911
NM_000257.4(MYH7):c.4481A>T (p.His1494Leu) rs727505329
NM_000257.4(MYH7):c.4487A>C (p.Glu1496Ala) rs397516218
NM_000257.4(MYH7):c.4519+1G>C rs876661374
NM_000257.4(MYH7):c.4525A>C (p.Ile1509Leu) rs397516221
NM_000257.4(MYH7):c.4537A>T (p.Thr1513Ser) rs397516222
NM_000257.4(MYH7):c.4540G>A (p.Glu1514Lys) rs397516223
NM_000257.4(MYH7):c.4588C>T (p.Arg1530Ter) rs397516225
NM_000257.4(MYH7):c.4644+3G>A rs397516226
NM_000257.4(MYH7):c.4663G>C (p.Glu1555Gln) rs727505176
NM_000257.4(MYH7):c.4679G>A (p.Arg1560Gln) rs730880806
NM_000257.4(MYH7):c.4717G>A (p.Glu1573Lys) rs750987717
NM_000257.4(MYH7):c.4720C>T (p.Arg1574Trp) rs397516227
NM_000257.4(MYH7):c.4721G>A (p.Arg1574Gln) rs779715863
NM_000257.4(MYH7):c.4816C>T (p.Arg1606Cys) rs200530211
NM_000257.4(MYH7):c.4817G>A (p.Arg1606His) rs373514686
NM_000257.4(MYH7):c.4826_4828delinsGCCGCAACC (p.Asn1609_Glu1610delinsSerArgAsnGln) rs1555336439
NM_000257.4(MYH7):c.4832C>T (p.Ala1611Val) rs757090529
NM_000257.4(MYH7):c.4834C>G (p.Leu1612Val) rs397516229
NM_000257.4(MYH7):c.4838G>A (p.Arg1613Lys) rs397516230
NM_000257.4(MYH7):c.4864C>T (p.Leu1622Phe) rs397516231
NM_000257.4(MYH7):c.4900C>T (p.Arg1634Cys) rs397516232
NM_000257.4(MYH7):c.4909G>A (p.Ala1637Thr) rs141122361
NM_000257.4(MYH7):c.4915G>A (p.Ala1639Thr) rs864309553
NM_000257.4(MYH7):c.4954-14C>G rs727505070
NM_000257.4(MYH7):c.4954G>T (p.Asp1652Tyr) rs397516233
NM_000257.4(MYH7):c.4985G>A (p.Arg1662His) rs370328209
NM_000257.4(MYH7):c.4992C>T (p.Asn1664=) rs763538103
NM_000257.4(MYH7):c.5015_5020del (p.Ala1672_Ile1673del) rs397516234
NM_000257.4(MYH7):c.5020G>A (p.Val1674Met) rs397516235
NM_000257.4(MYH7):c.5065C>T (p.Arg1689Cys) rs730880915
NM_000257.4(MYH7):c.5067_5079delinsGGCCGTGGAAGAA (p.Val1692Glu) rs727505033
NM_000257.4(MYH7):c.5071G>A (p.Val1691Met) rs45464193
NM_000257.4(MYH7):c.5088G>C (p.Glu1696Asp) rs373219734
NM_000257.4(MYH7):c.5096G>A (p.Arg1699Gln) rs146778113
NM_000257.4(MYH7):c.5110C>T (p.Gln1704Ter) rs727504844
NM_000257.4(MYH7):c.5134C>T (p.Arg1712Trp) rs121913650
NM_000257.4(MYH7):c.5156A>G (p.Gln1719Arg) rs727504403
NM_000257.4(MYH7):c.5191G>A (p.Asp1731Asn) rs876657885
NM_000257.4(MYH7):c.5192A>T (p.Asp1731Val) rs397516240

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