ClinVar Miner

List of variants in gene combination LOC126861897, MYH7 reported by Labcorp Genetics (formerly Invitae), Labcorp

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Total variants: 64
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HGVS dbSNP gnomAD frequency
NM_000257.4(MYH7):c.5283+19C>T rs45582836 0.00020
NM_000257.4(MYH7):c.5287G>A (p.Ala1763Thr) rs727504355 0.00009
NM_000257.4(MYH7):c.5243G>A (p.Cys1748Tyr) rs200303340 0.00005
NM_000257.4(MYH7):c.5253T>C (p.Ala1751=) rs776282574 0.00004
NM_000257.4(MYH7):c.5305C>A (p.Leu1769Met) rs139222507 0.00004
NM_000257.4(MYH7):c.5280G>A (p.Thr1760=) rs374803185 0.00003
NM_000257.4(MYH7):c.5283+18C>G rs746278750 0.00002
NM_000257.4(MYH7):c.5283+20G>T rs771626451 0.00002
NM_000257.4(MYH7):c.5283+7C>T rs772148835 0.00002
NM_000257.4(MYH7):c.5286C>T (p.Ala1762=) rs771432461 0.00002
NM_000257.4(MYH7):c.5216C>T (p.Thr1739Ile) rs1469341108 0.00001
NM_000257.4(MYH7):c.5222T>C (p.Val1741Ala) rs531250955 0.00001
NM_000257.4(MYH7):c.5229G>T (p.Glu1743Asp) rs149509691 0.00001
NM_000257.4(MYH7):c.5245A>C (p.Arg1749=) rs562465062 0.00001
NM_000257.4(MYH7):c.5251G>A (p.Ala1751Thr) rs1892151210 0.00001
NM_000257.4(MYH7):c.5272G>T (p.Ala1758Ser) rs878853839 0.00001
NM_000257.4(MYH7):c.5279C>T (p.Thr1760Met) rs727505294 0.00001
NM_000257.4(MYH7):c.5283+20G>A rs771626451 0.00001
NM_000257.4(MYH7):c.5284-17C>T rs767904246 0.00001
NM_000257.4(MYH7):c.5284-3C>T rs759821521 0.00001
NM_000257.4(MYH7):c.5293A>G (p.Met1765Val) rs770165807 0.00001
NM_000257.4(MYH7):c.5221G>A (p.Val1741Met) rs1255832799
NM_000257.4(MYH7):c.5228A>G (p.Glu1743Gly) rs1892152784
NM_000257.4(MYH7):c.5234T>C (p.Val1745Ala) rs767027931
NM_000257.4(MYH7):c.5241G>T (p.Glu1747Asp)
NM_000257.4(MYH7):c.5245A>G (p.Arg1749Gly) rs562465062
NM_000257.4(MYH7):c.5248A>G (p.Asn1750Asp) rs2138639378
NM_000257.4(MYH7):c.5249A>G (p.Asn1750Ser)
NM_000257.4(MYH7):c.5252C>A (p.Ala1751Asp) rs893202710
NM_000257.4(MYH7):c.5254G>A (p.Glu1752Lys) rs730880916
NM_000257.4(MYH7):c.5254GAG[1] (p.Glu1753del) rs2138639303
NM_000257.4(MYH7):c.5255A>G (p.Glu1752Gly) rs730880813
NM_000257.4(MYH7):c.5257_5265dup (p.Ala1755_Lys1756insGluLysAla) rs2502240701
NM_000257.4(MYH7):c.5258AGAAGGCCA[1] (p.Lys1756_Ala1758del) rs1566522846
NM_000257.4(MYH7):c.5258AGAAGGCCA[3] (p.Lys1756_Ala1758dup) rs1566522846
NM_000257.4(MYH7):c.5261A>T (p.Lys1754Met) rs2138639298
NM_000257.4(MYH7):c.5262G>A (p.Lys1754=) rs2502240720
NM_000257.4(MYH7):c.5263G>T (p.Ala1755Ser) rs730880814
NM_000257.4(MYH7):c.5265C>A (p.Ala1755=) rs2138639281
NM_000257.4(MYH7):c.5267A>G (p.Lys1756Arg) rs1566522855
NM_000257.4(MYH7):c.5270A>G (p.Lys1757Arg) rs2138639265
NM_000257.4(MYH7):c.5272G>A (p.Ala1758Thr) rs878853839
NM_000257.4(MYH7):c.5279C>A (p.Thr1760Lys) rs727505294
NM_000257.4(MYH7):c.5281G>A (p.Asp1761Asn) rs1306082414
NM_000257.4(MYH7):c.5283+11del rs1356309919
NM_000257.4(MYH7):c.5283+13C>T rs2138639162
NM_000257.4(MYH7):c.5283+15C>T rs1052787042
NM_000257.4(MYH7):c.5283+1G>T
NM_000257.4(MYH7):c.5283+2T>C rs2138639201
NM_000257.4(MYH7):c.5283+4A>G rs1892148705
NM_000257.4(MYH7):c.5283+6_5283+11del rs2138639172
NM_000257.4(MYH7):c.5283+9C>G rs1595072148
NM_000257.4(MYH7):c.5284-16T>A rs2502240064
NM_000257.4(MYH7):c.5284-7C>A rs2502240020
NM_000257.4(MYH7):c.5284-9T>C
NM_000257.4(MYH7):c.5287G>T (p.Ala1763Ser) rs727504355
NM_000257.4(MYH7):c.5291T>C (p.Met1764Thr) rs1284464290
NM_000257.4(MYH7):c.5291T>G (p.Met1764Arg)
NM_000257.4(MYH7):c.5292G>A (p.Met1764Ile) rs2502239927
NM_000257.4(MYH7):c.5294T>A (p.Met1765Lys) rs1595072009
NM_000257.4(MYH7):c.5296G>A (p.Ala1766Thr) rs267606909
NM_000257.4(MYH7):c.5302G>A (p.Glu1768Lys) rs397516241
NM_000257.4(MYH7):c.5304G>A (p.Glu1768=) rs1231303625
NM_000257.4(MYH7):c.5306T>C (p.Leu1769Pro) rs1892140874

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