ClinVar Miner

List of variants in gene MYH9 reported as uncertain significance by Invitae

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Gene type:
ClinVar version:
Total variants: 179
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HGVS dbSNP gnomAD frequency
NM_002473.6(MYH9):c.4556G>A (p.Ser1519Asn) rs138193963 0.00016
NM_002473.6(MYH9):c.5081G>A (p.Arg1694His) rs538330756 0.00006
NM_002473.6(MYH9):c.4297C>T (p.Arg1433Cys) rs727503286 0.00005
NM_002473.6(MYH9):c.1057G>A (p.Val353Ile) rs375702969 0.00004
NM_002473.6(MYH9):c.2159+6C>T rs748916231 0.00004
NM_002473.6(MYH9):c.1519G>A (p.Asp507Asn) rs377410439 0.00003
NM_002473.6(MYH9):c.233C>T (p.Pro78Leu) rs150313549 0.00003
NM_002473.6(MYH9):c.3181A>T (p.Ser1061Cys) rs199971000 0.00003
NM_002473.6(MYH9):c.4897C>T (p.Arg1633Trp) rs757547632 0.00003
NM_002473.6(MYH9):c.5695G>A (p.Glu1899Lys) rs747131828 0.00003
NM_002473.6(MYH9):c.1380T>C (p.Asp460=) rs876657891 0.00002
NM_002473.6(MYH9):c.4025G>A (p.Arg1342Gln) rs758159686 0.00002
NM_002473.6(MYH9):c.4670G>A (p.Arg1557Gln) rs373393111 0.00002
NM_002473.6(MYH9):c.2077C>T (p.Arg693Cys) rs751852988 0.00001
NM_002473.6(MYH9):c.2405G>A (p.Arg802Gln) rs765414397 0.00001
NM_002473.6(MYH9):c.5308C>T (p.Arg1770Cys) rs1430793034 0.00001
NM_002473.6(MYH9):c.5833G>A (p.Glu1945Lys) rs1478233597 0.00001
NC_000022.10:g.(?_36744929)_(36745281_?)dup
NM_002473.6(MYH9):c.1072C>T (p.Arg358Trp)
NM_002473.6(MYH9):c.1093A>G (p.Met365Val)
NM_002473.6(MYH9):c.1096C>T (p.Pro366Ser)
NM_002473.6(MYH9):c.1102A>G (p.Asn368Asp)
NM_002473.6(MYH9):c.1120G>A (p.Val374Met)
NM_002473.6(MYH9):c.1136G>A (p.Gly379Asp)
NM_002473.6(MYH9):c.115A>G (p.Ser39Gly) rs2017727253
NM_002473.6(MYH9):c.1160G>A (p.Arg387Lys)
NM_002473.6(MYH9):c.1177C>T (p.Arg393Cys) rs1156464508
NM_002473.6(MYH9):c.121T>A (p.Phe41Ile)
NM_002473.6(MYH9):c.1273A>T (p.Met425Leu) rs961182177
NM_002473.6(MYH9):c.139A>G (p.Lys47Glu)
NM_002473.6(MYH9):c.139_141del (p.Lys47del)
NM_002473.6(MYH9):c.1481G>A (p.Arg494His)
NM_002473.6(MYH9):c.1615G>A (p.Asp539Asn)
NM_002473.6(MYH9):c.1617C>G (p.Asp539Glu)
NM_002473.6(MYH9):c.1651G>T (p.Gly551Cys)
NM_002473.6(MYH9):c.166G>A (p.Val56Met)
NM_002473.6(MYH9):c.1738A>G (p.Lys580Glu)
NM_002473.6(MYH9):c.173T>G (p.Leu58Arg)
NM_002473.6(MYH9):c.1786A>G (p.Ile596Val)
NM_002473.6(MYH9):c.1807T>G (p.Ser603Ala)
NM_002473.6(MYH9):c.1827G>A (p.Ser609=)
NM_002473.6(MYH9):c.1844T>C (p.Val615Ala)
NM_002473.6(MYH9):c.1850G>A (p.Arg617His)
NM_002473.6(MYH9):c.1864G>A (p.Asp622Asn)
NM_002473.6(MYH9):c.1883C>T (p.Ser628Leu)
NM_002473.6(MYH9):c.1891G>A (p.Ala631Thr)
NM_002473.6(MYH9):c.1913C>T (p.Thr638Met)
NM_002473.6(MYH9):c.1916G>A (p.Arg639Gln)
NM_002473.6(MYH9):c.1991C>T (p.Thr664Met)
NM_002473.6(MYH9):c.2000A>G (p.Asn667Ser) rs575821361
NM_002473.6(MYH9):c.2029G>C (p.Glu677Gln)
NM_002473.6(MYH9):c.2037+4C>T
NM_002473.6(MYH9):c.2038-3C>T
NM_002473.6(MYH9):c.2054C>T (p.Pro685Leu)
NM_002473.6(MYH9):c.2070C>A (p.Asp690Glu) rs2146348210
NM_002473.6(MYH9):c.2078G>A (p.Arg693His)
NM_002473.6(MYH9):c.2125C>T (p.Pro709Ser)
NM_002473.6(MYH9):c.2216C>T (p.Ala739Val)
NM_002473.6(MYH9):c.2221G>A (p.Val741Met)
NM_002473.6(MYH9):c.2288T>G (p.Phe763Cys)
NM_002473.6(MYH9):c.2309A>G (p.His770Arg) rs2146346627
NM_002473.6(MYH9):c.2398_2400delinsTTT (p.Ala800Phe)
NM_002473.6(MYH9):c.2441G>A (p.Arg814Gln)
NM_002473.6(MYH9):c.2449G>A (p.Ala817Thr)
NM_002473.6(MYH9):c.2462A>G (p.Lys821Arg)
NM_002473.6(MYH9):c.2468G>A (p.Arg823Gln)
NM_002473.6(MYH9):c.2499+4C>T
NM_002473.6(MYH9):c.2507C>T (p.Pro836Leu) rs1603483077
NM_002473.6(MYH9):c.2579A>G (p.Lys860Arg)
NM_002473.6(MYH9):c.257T>A (p.Met86Lys) rs774334908
NM_002473.6(MYH9):c.2626T>C (p.Ser876Pro)
NM_002473.6(MYH9):c.289G>T (p.Val97Leu)
NM_002473.6(MYH9):c.299A>T (p.Asn100Ile)
NM_002473.6(MYH9):c.3008A>C (p.Glu1003Ala)
NM_002473.6(MYH9):c.3046A>G (p.Lys1016Glu)
NM_002473.6(MYH9):c.3093C>G (p.Asp1031Glu) rs2146341663
NM_002473.6(MYH9):c.3122A>T (p.Lys1041Met)
NM_002473.6(MYH9):c.3124_3144dup (p.Lys1048_Thr1049insGlnArgGlnGluLeuGluLys)
NM_002473.6(MYH9):c.3128G>T (p.Arg1043Leu)
NM_002473.6(MYH9):c.3148C>T (p.Arg1050Cys)
NM_002473.6(MYH9):c.3177C>A (p.Asp1059Glu)
NM_002473.6(MYH9):c.3205_3225del (p.Ala1069_Lys1075del) rs2146339780
NM_002473.6(MYH9):c.3215C>A (p.Ala1072Glu)
NM_002473.6(MYH9):c.3230A>C (p.Gln1077Pro)
NM_002473.6(MYH9):c.3272+3G>T rs1238385506
NM_002473.6(MYH9):c.3289G>T (p.Ala1097Ser)
NM_002473.6(MYH9):c.3323A>C (p.Glu1108Ala)
NM_002473.6(MYH9):c.333+3A>G
NM_002473.6(MYH9):c.333C>T (p.Tyr111=)
NM_002473.6(MYH9):c.3404G>A (p.Arg1135Gln)
NM_002473.6(MYH9):c.3485+3G>T
NM_002473.6(MYH9):c.3485+6C>T
NM_002473.6(MYH9):c.3505G>T (p.Val1169Leu)
NM_002473.6(MYH9):c.3562C>G (p.Gln1188Glu) rs2016766439
NM_002473.6(MYH9):c.3608A>G (p.Glu1203Gly)
NM_002473.6(MYH9):c.3628C>T (p.Arg1210Trp)
NM_002473.6(MYH9):c.3630+5G>A
NM_002473.6(MYH9):c.3646G>A (p.Glu1216Lys)
NM_002473.6(MYH9):c.3673G>A (p.Glu1225Lys) rs770864107
NM_002473.6(MYH9):c.3679G>T (p.Gly1227Trp)
NM_002473.6(MYH9):c.3694G>A (p.Glu1232Lys) rs1569534975
NM_002473.6(MYH9):c.3700A>C (p.Lys1234Gln)
NM_002473.6(MYH9):c.3737A>G (p.Lys1246Arg)
NM_002473.6(MYH9):c.3838-7G>A
NM_002473.6(MYH9):c.3838G>A (p.Val1280Met) rs141582478
NM_002473.6(MYH9):c.3868A>G (p.Ser1290Gly)
NM_002473.6(MYH9):c.3886T>G (p.Ser1296Ala)
NM_002473.6(MYH9):c.3904G>T (p.Asp1302Tyr)
NM_002473.6(MYH9):c.3907T>C (p.Phe1303Leu)
NM_002473.6(MYH9):c.3940C>G (p.Gln1314Glu)
NM_002473.6(MYH9):c.3942+5G>A rs775695035
NM_002473.6(MYH9):c.3942+5G>C
NM_002473.6(MYH9):c.3968A>G (p.Gln1323Arg)
NM_002473.6(MYH9):c.406G>A (p.Glu136Lys)
NM_002473.6(MYH9):c.418G>T (p.Gly140Cys)
NM_002473.6(MYH9):c.4196A>G (p.Gln1399Arg) rs2146335439
NM_002473.6(MYH9):c.4222T>C (p.Tyr1408His)
NM_002473.6(MYH9):c.4250G>A (p.Arg1417Gln) rs2016714761
NM_002473.6(MYH9):c.4274_4294dup (p.His1431_Gln1432insLeuLeuValAspLeuAspHis)
NM_002473.6(MYH9):c.4307C>T (p.Ala1436Val)
NM_002473.6(MYH9):c.4310G>A (p.Cys1437Tyr)
NM_002473.6(MYH9):c.4337T>C (p.Phe1446Ser)
NM_002473.6(MYH9):c.4340A>G (p.Asp1447Gly) rs797044804
NM_002473.6(MYH9):c.4341C>A (p.Asp1447Glu)
NM_002473.6(MYH9):c.4354GAG[1] (p.Glu1453del)
NM_002473.6(MYH9):c.4357G>A (p.Glu1453Lys)
NM_002473.6(MYH9):c.4447C>T (p.Arg1483Trp) rs368105628
NM_002473.6(MYH9):c.4561C>G (p.His1521Asp)
NM_002473.6(MYH9):c.4660G>T (p.Ala1554Ser)
NM_002473.6(MYH9):c.4682A>G (p.Asn1561Ser)
NM_002473.6(MYH9):c.4688A>G (p.Gln1563Arg)
NM_002473.6(MYH9):c.4704G>C (p.Gln1568His)
NM_002473.6(MYH9):c.4708G>A (p.Glu1570Lys)
NM_002473.6(MYH9):c.4775G>A (p.Arg1592Gln)
NM_002473.6(MYH9):c.4953G>T (p.Met1651Ile)
NM_002473.6(MYH9):c.4963G>C (p.Asp1655His)
NM_002473.6(MYH9):c.4964A>G (p.Asp1655Gly)
NM_002473.6(MYH9):c.4975G>A (p.Ala1659Thr)
NM_002473.6(MYH9):c.5014G>A (p.Glu1672Lys)
NM_002473.6(MYH9):c.5048T>C (p.Ile1683Thr)
NM_002473.6(MYH9):c.5080C>T (p.Arg1694Cys)
NM_002473.6(MYH9):c.50T>C (p.Ile17Thr)
NM_002473.6(MYH9):c.5100G>C (p.Gln1700His) rs2016572846
NM_002473.6(MYH9):c.5174_5175delinsAA (p.Arg1725Gln)
NM_002473.6(MYH9):c.518+4A>G rs2017354123
NM_002473.6(MYH9):c.5245A>G (p.Asn1749Asp)
NM_002473.6(MYH9):c.5248G>A (p.Asp1750Asn)
NM_002473.6(MYH9):c.5275-7_5275-5del rs780656298
NM_002473.6(MYH9):c.5309G>T (p.Arg1770Leu) rs746118702
NM_002473.6(MYH9):c.5314C>T (p.His1772Tyr) rs1455355336
NM_002473.6(MYH9):c.5329G>A (p.Glu1777Lys)
NM_002473.6(MYH9):c.5339_5341del (p.Arg1780del) rs2146328050
NM_002473.6(MYH9):c.5360A>G (p.Asn1787Ser)
NM_002473.6(MYH9):c.5374G>A (p.Val1792Ile)
NM_002473.6(MYH9):c.544G>A (p.Glu182Lys)
NM_002473.6(MYH9):c.5483+4C>T rs56327920
NM_002473.6(MYH9):c.5483+5G>C
NM_002473.6(MYH9):c.5498C>T (p.Ala1833Val)
NM_002473.6(MYH9):c.54C>A (p.Asn18Lys)
NM_002473.6(MYH9):c.5592+7G>A
NM_002473.6(MYH9):c.5596G>C (p.Asp1866His)
NM_002473.6(MYH9):c.5597A>G (p.Asp1866Gly)
NM_002473.6(MYH9):c.5629C>T (p.Arg1877Trp)
NM_002473.6(MYH9):c.5644G>A (p.Ala1882Thr)
NM_002473.6(MYH9):c.5659C>G (p.Gln1887Glu)
NM_002473.6(MYH9):c.5706C>G (p.Asp1902Glu)
NM_002473.6(MYH9):c.5722G>A (p.Asp1908Asn)
NM_002473.6(MYH9):c.5765+4A>G
NM_002473.6(MYH9):c.5773G>A (p.Asp1925Asn)
NM_002473.6(MYH9):c.580G>A (p.Val194Met)
NM_002473.6(MYH9):c.719G>T (p.Arg240Leu)
NM_002473.6(MYH9):c.723C>T (p.Ile241=)
NM_002473.6(MYH9):c.729T>G (p.Phe243Leu)
NM_002473.6(MYH9):c.796C>T (p.Arg266Cys)
NM_002473.6(MYH9):c.815G>A (p.Arg272Gln)
NM_002473.6(MYH9):c.854G>C (p.Gly285Ala) rs1188816913
NM_002473.6(MYH9):c.871G>A (p.Asp291Asn)
NM_002473.6(MYH9):c.898T>C (p.Tyr300His)
NM_002473.6(MYH9):c.906C>G (p.Phe302Leu)

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