ClinVar Miner

List of variants in gene MYH6 reported by PreventionGenetics, part of Exact Sciences

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Gene type:
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Total variants: 117
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HGVS dbSNP gnomAD frequency
NM_002471.4(MYH6):c.800-11A>G rs434273 0.81807
NM_002471.4(MYH6):c.4526-34T>C rs178642 0.47911
NM_002471.4(MYH6):c.4359+13C>T rs8022522 0.46131
NM_002471.4(MYH6):c.3302T>C (p.Val1101Ala) rs365990 0.44987
NM_002471.4(MYH6):c.2292+18C>T rs452036 0.42619
NM_002471.4(MYH6):c.1962+39T>C rs412768 0.35458
NM_002471.4(MYH6):c.1582-39C>T rs439735 0.22818
NM_002471.4(MYH6):c.5565+22A>G rs8006357 0.22619
NM_002471.4(MYH6):c.3388G>A (p.Ala1130Thr) rs28730771 0.08821
NM_002471.4(MYH6):c.5598A>G (p.Leu1866=) rs17091278 0.08756
NM_002471.4(MYH6):c.4011G>A (p.Ser1337=) rs451794 0.07834
NM_002471.4(MYH6):c.5164-22A>G rs178637 0.07783
NM_002471.4(MYH6):c.5259C>T (p.Ala1753=) rs8004990 0.07782
NM_002471.4(MYH6):c.1335C>T (p.Asn445=) rs61731179 0.03984
NM_002471.4(MYH6):c.999C>T (p.Thr333=) rs78107039 0.03596
NM_002471.4(MYH6):c.4527G>A (p.Glu1509=) rs34855944 0.02632
NM_002471.4(MYH6):c.2151C>T (p.Tyr717=) rs76202964 0.01414
NM_002471.4(MYH6):c.1989C>T (p.Asn663=) rs28730774 0.00451
NM_002471.4(MYH6):c.4395G>A (p.Ser1465=) rs74039310 0.00368
NM_002471.4(MYH6):c.2071G>A (p.Val691Ile) rs148915045 0.00284
NM_002471.4(MYH6):c.1275C>T (p.Ile425=) rs61742470 0.00232
NM_002471.4(MYH6):c.1763A>C (p.Asp588Ala) rs142992009 0.00153
NM_002471.4(MYH6):c.3979-15C>A rs529249069 0.00146
NM_002471.4(MYH6):c.3979-7T>G rs535111647 0.00142
NM_002471.4(MYH6):c.5400C>T (p.Asp1800=) rs144329079 0.00141
NM_002471.4(MYH6):c.1122G>A (p.Ala374=) rs148091079 0.00116
NM_002471.4(MYH6):c.3010G>T (p.Ala1004Ser) rs143978652 0.00110
NM_002471.4(MYH6):c.2430-14C>T rs190342289 0.00108
NM_002471.4(MYH6):c.1083G>T (p.Gly361=) rs138928022 0.00092
NM_002471.4(MYH6):c.5601G>A (p.Gln1867=) rs148984154 0.00062
NM_002471.4(MYH6):c.5652C>T (p.Ala1884=) rs200662317 0.00062
NM_002471.4(MYH6):c.4193G>A (p.Arg1398Gln) rs150815925 0.00041
NM_002471.4(MYH6):c.643-5C>T rs199859986 0.00041
NM_002471.4(MYH6):c.4611G>A (p.Val1537=) rs142983918 0.00030
NM_002471.4(MYH6):c.4293G>A (p.Met1431Ile) rs201016285 0.00029
NM_002471.4(MYH6):c.5410C>A (p.Gln1804Lys) rs144571463 0.00029
NM_002471.4(MYH6):c.981C>T (p.Ser327=) rs148407931 0.00029
NM_002471.4(MYH6):c.2685+10C>T rs202155137 0.00024
NM_002471.4(MYH6):c.4359+10G>A rs368183862 0.00024
NM_002471.4(MYH6):c.4137G>A (p.Thr1379=) rs372158844 0.00022
NM_002471.4(MYH6):c.4505G>A (p.Arg1502Gln) rs199936506 0.00022
NM_002471.4(MYH6):c.3383G>A (p.Arg1128His) rs376002621 0.00021
NM_002471.4(MYH6):c.2841C>T (p.Asp947=) rs140305424 0.00019
NM_002471.4(MYH6):c.824T>A (p.Ile275Asn) rs201327273 0.00019
NM_002471.4(MYH6):c.3894G>A (p.Ala1298=) rs151135141 0.00016
NM_002471.4(MYH6):c.1410C>T (p.Asp470=) rs139886074 0.00011
NM_002471.4(MYH6):c.2973C>T (p.Ile991=) rs374807345 0.00011
NM_002471.4(MYH6):c.678C>T (p.Pro226=) rs768893926 0.00011
NM_002471.4(MYH6):c.1662C>T (p.Tyr554=) rs374114140 0.00010
NM_002471.4(MYH6):c.3988G>A (p.Ala1330Thr) rs757840030 0.00007
NM_002471.4(MYH6):c.1628A>G (p.Lys543Arg) rs367663906 0.00006
NM_002471.4(MYH6):c.3787G>A (p.Val1263Met) rs375819633 0.00006
NM_002471.4(MYH6):c.5458C>T (p.Arg1820Trp) rs111473291 0.00006
NM_002471.4(MYH6):c.1087A>T (p.Met363Leu) rs202196487 0.00005
NM_002471.4(MYH6):c.5427A>C (p.Gly1809=) rs149294569 0.00005
NM_002471.4(MYH6):c.5661+9A>G rs373908250 0.00005
NM_002471.4(MYH6):c.1381C>T (p.Leu461=) rs368609214 0.00004
NM_002471.4(MYH6):c.5594G>A (p.Arg1865Gln) rs138720701 0.00004
NM_002471.4(MYH6):c.2018G>A (p.Arg673His) rs1023327699 0.00003
NM_002471.4(MYH6):c.2127G>A (p.Lys709=) rs765316931 0.00003
NM_002471.4(MYH6):c.2141G>A (p.Arg714His) rs776602843 0.00003
NM_002471.4(MYH6):c.5780G>T (p.Arg1927Leu) rs730880152 0.00003
NM_002471.4(MYH6):c.1086C>T (p.Asn362=) rs375189593 0.00002
NM_002471.4(MYH6):c.1575C>T (p.Ile525=) rs756615422 0.00002
NM_002471.4(MYH6):c.2271G>A (p.Gln757=) rs777100730 0.00002
NM_002471.4(MYH6):c.2533G>A (p.Ala845Thr) rs989813600 0.00002
NM_002471.4(MYH6):c.4470C>T (p.Tyr1490=) rs727504964 0.00002
NM_002471.4(MYH6):c.5439G>A (p.Gln1813=) rs200854143 0.00002
NM_002471.4(MYH6):c.5660C>T (p.Ala1887Val) rs767096302 0.00002
NM_002471.4(MYH6):c.5695C>T (p.Arg1899Cys) rs371607892 0.00002
NM_002471.4(MYH6):c.1227C>T (p.Asn409=) rs752919716 0.00001
NM_002471.4(MYH6):c.1492G>A (p.Glu498Lys) rs375142167 0.00001
NM_002471.4(MYH6):c.1791A>T (p.Lys597Asn) rs1252826013 0.00001
NM_002471.4(MYH6):c.2336G>A (p.Arg779Gln) rs1486610243 0.00001
NM_002471.4(MYH6):c.2980C>A (p.Leu994Met) rs727503238 0.00001
NM_002471.4(MYH6):c.3140G>A (p.Arg1047His) rs775843647 0.00001
NM_002471.4(MYH6):c.3506G>A (p.Arg1169His) rs975923796 0.00001
NM_002471.4(MYH6):c.3758C>T (p.Thr1253Met) rs201051663 0.00001
NM_002471.4(MYH6):c.3836G>A (p.Arg1279Gln) rs200014711 0.00001
NM_002471.4(MYH6):c.4150C>T (p.Arg1384Trp) rs763926580 0.00001
NM_002471.4(MYH6):c.4279A>T (p.Ile1427Leu) rs1194099606 0.00001
NM_002471.4(MYH6):c.4465G>A (p.Ala1489Thr) rs761539900 0.00001
NM_002471.4(MYH6):c.5623C>T (p.Leu1875=) rs368604132 0.00001
NM_002471.3(MYH6):c.3979-8C>A rs555976716
NM_002471.4(MYH6):c.1003A>G (p.Ser335Gly)
NM_002471.4(MYH6):c.1034A>T (p.Glu345Val) rs561344265
NM_002471.4(MYH6):c.1138G>A (p.Glu380Lys) rs768924353
NM_002471.4(MYH6):c.1301A>C (p.Glu434Ala) rs758220970
NM_002471.4(MYH6):c.1425G>C (p.Glu475Asp) rs397516755
NM_002471.4(MYH6):c.1581+10del rs560271582
NM_002471.4(MYH6):c.1595T>C (p.Met532Thr)
NM_002471.4(MYH6):c.1946T>C (p.Val649Ala)
NM_002471.4(MYH6):c.2033A>G (p.Asn678Ser) rs515726230
NM_002471.4(MYH6):c.2736A>G (p.Lys912=)
NM_002471.4(MYH6):c.2891C>T (p.Ala964Val)
NM_002471.4(MYH6):c.3979-10C>G rs28730768
NM_002471.4(MYH6):c.3979-14C>A rs372226248
NM_002471.4(MYH6):c.3979-3dup rs770492637
NM_002471.4(MYH6):c.3979-7_3979-6del rs796313537
NM_002471.4(MYH6):c.3979-8del rs193922652
NM_002471.4(MYH6):c.3979-9C>A rs57660219
NM_002471.4(MYH6):c.3979-9C>G rs57660219
NM_002471.4(MYH6):c.4207G>A (p.Glu1403Lys) rs769398160
NM_002471.4(MYH6):c.4357A>C (p.Lys1453Gln)
NM_002471.4(MYH6):c.4360-7C>T rs58949384
NM_002471.4(MYH6):c.4504C>T (p.Arg1502Trp) rs773631723
NM_002471.4(MYH6):c.4595G>T (p.Arg1532Leu) rs34330111
NM_002471.4(MYH6):c.5290G>A (p.Ala1764Thr)
NM_002471.4(MYH6):c.5335G>T (p.Ala1779Ser)
NM_002471.4(MYH6):c.5404G>A (p.Ala1802Thr)
NM_002471.4(MYH6):c.5476_5477delinsAA (p.Gly1826Asn) rs878854502
NM_002471.4(MYH6):c.5731C>T (p.Arg1911Trp)
NM_002471.4(MYH6):c.5780G>A (p.Arg1927His) rs730880152
NM_002471.4(MYH6):c.644G>T (p.Gly215Val)
NM_002471.4(MYH6):c.694G>A (p.Gly232Ser) rs587782960
NM_002471.4(MYH6):c.843G>C (p.Glu281Asp)
NM_002471.4(MYH6):c.872T>C (p.Leu291Pro)

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