ClinVar Miner

List of variants in gene combination MYH8, MYHAS reported as likely benign

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Gene type:
ClinVar version:
Total variants: 80
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HGVS dbSNP gnomAD frequency
NM_002472.3(MYH8):c.*76G>C rs3744551 0.02944
NM_002472.3(MYH8):c.2171+82T>A rs148245264 0.02040
NM_002472.3(MYH8):c.1701G>A (p.Gln567=) rs73275411 0.01912
NM_002472.3(MYH8):c.4233C>T (p.Asn1411=) rs138992963 0.01251
NM_002472.3(MYH8):c.1416+215G>A rs9889712 0.00940
NM_002472.3(MYH8):c.3736-263C>T rs28653529 0.00885
NM_002472.3(MYH8):c.1147+147C>G rs9902705 0.00883
NM_002472.3(MYH8):c.1147+15T>G rs115518385 0.00809
NM_002472.3(MYH8):c.4178+120dup rs201916027 0.00730
NM_002472.3(MYH8):c.-30-104G>C rs79815072 0.00680
NM_002472.3(MYH8):c.3686T>C (p.Met1229Thr) rs35962914 0.00663
NM_002472.3(MYH8):c.3757C>T (p.Arg1253Cys) rs34953692 0.00448
NM_002472.3(MYH8):c.805+9C>T rs75468422 0.00426
NM_002472.3(MYH8):c.1632T>C (p.Pro544=) rs144596237 0.00409
NM_002472.3(MYH8):c.*72T>C rs184845947 0.00388
NM_002472.3(MYH8):c.2432+6A>C rs111692916 0.00351
NM_002472.3(MYH8):c.211-218C>T rs542389644 0.00350
NM_002472.3(MYH8):c.4740A>C (p.Ala1580=) rs61730806 0.00347
NM_002472.3(MYH8):c.540C>T (p.Thr180=) rs34613390 0.00340
NM_002472.3(MYH8):c.4499C>T (p.Thr1500Met) rs73977155 0.00334
NM_002472.3(MYH8):c.4179-194C>T rs149267669 0.00332
NM_002472.3(MYH8):c.4962+137T>C rs149761278 0.00316
NM_002472.3(MYH8):c.4179-137C>T rs138389156 0.00309
NC_000017.11:g.10390312del rs112236252 0.00300
NM_002472.3(MYH8):c.2174dup (p.Tyr725Ter) rs565515290 0.00261
NM_002472.3(MYH8):c.2147T>A (p.Ile716Asn) rs115483891 0.00218
NM_002472.3(MYH8):c.4813G>A (p.Asp1605Asn) rs139344968 0.00209
NM_002472.3(MYH8):c.1209C>A (p.Cys403Ter) rs144321381 0.00124
NM_002472.3(MYH8):c.143C>T (p.Ser48Phe) rs146669648 0.00101
NM_002472.3(MYH8):c.4042G>A (p.Glu1348Lys) rs140562514 0.00083
NM_002472.3(MYH8):c.954G>C (p.Gln318His) rs142606252 0.00081
NM_002472.3(MYH8):c.2274A>G (p.Gln758=) rs145901155 0.00080
NM_002472.3(MYH8):c.430G>C (p.Ala144Pro) rs138262102 0.00065
NM_002472.3(MYH8):c.4878T>C (p.Asn1626=) rs202123184 0.00055
NM_002472.3(MYH8):c.1731G>C (p.Glu577Asp) rs75160168 0.00053
NM_002472.3(MYH8):c.4786G>A (p.Val1596Ile) rs61730807 0.00052
NM_002472.3(MYH8):c.578G>A (p.Arg193His) rs145863180 0.00052
NM_002472.3(MYH8):c.1318C>T (p.Leu440=) rs141899271 0.00049
NM_002472.3(MYH8):c.4784G>C (p.Arg1595Thr) rs145711576 0.00048
NM_002472.3(MYH8):c.4147A>G (p.Ile1383Val) rs138607111 0.00045
NM_002472.3(MYH8):c.2117G>A (p.Arg706His) rs150351713 0.00020
NM_002472.3(MYH8):c.304C>G (p.Pro102Ala) rs149941951 0.00014
NM_002472.3(MYH8):c.676G>A (p.Ala226Thr) rs140408926 0.00013
NM_002472.3(MYH8):c.741+8T>C rs370684142 0.00013
NM_002472.3(MYH8):c.1815T>A (p.Asn605Lys) rs151091483 0.00012
NM_002472.3(MYH8):c.1905C>T (p.Ser635=) rs377372606 0.00011
NM_002472.3(MYH8):c.2055G>A (p.Gly685=) rs761674430 0.00011
NM_002472.3(MYH8):c.675C>T (p.Ser225=) rs146651214 0.00009
NM_002472.3(MYH8):c.1155C>T (p.Asp385=) rs140617211 0.00007
NM_002472.3(MYH8):c.4353C>T (p.Asn1451=) rs756865778 0.00007
NM_002472.3(MYH8):c.479T>A (p.Ile160Asn) rs760980150 0.00007
NM_002472.3(MYH8):c.539+1G>A rs149198713 0.00006
NM_002472.3(MYH8):c.417C>T (p.Pro139=) rs531526832 0.00005
NM_002472.3(MYH8):c.1380C>T (p.Ile460=) rs778977499 0.00004
NM_002472.3(MYH8):c.1734C>T (p.Ala578=) rs144464113 0.00004
NM_002472.3(MYH8):c.1833G>A (p.Leu611=) rs202061555 0.00003
NM_002472.3(MYH8):c.4235C>T (p.Ala1412Val) rs750806957 0.00002
NM_002472.3(MYH8):c.1663C>T (p.Leu555=) rs1481974689 0.00001
NM_002472.3(MYH8):c.1770C>T (p.Asp590=) rs1555557227 0.00001
NM_002472.3(MYH8):c.2432+8T>C rs761265244 0.00001
NM_002472.3(MYH8):c.351C>T (p.Ile117=) rs752219854 0.00001
NM_002472.3(MYH8):c.355-9T>C rs776667568 0.00001
NM_002472.3(MYH8):c.405G>A (p.Pro135=) rs775704195 0.00001
NM_002472.3(MYH8):c.4158A>C (p.Thr1386=) rs543637171 0.00001
NM_002472.3(MYH8):c.4962+7G>A rs770966811 0.00001
NM_002472.3(MYH8):c.105T>C (p.Asp35=)
NM_002472.3(MYH8):c.1408del (p.Ile470fs) rs1060499728
NM_002472.3(MYH8):c.1548T>C (p.Phe516=) rs2508071671
NM_002472.3(MYH8):c.1755T>C (p.Tyr585=) rs1597402818
NM_002472.3(MYH8):c.2433-167_2433-166insCGTGTG rs1555556565
NM_002472.3(MYH8):c.3862+276CA[10] rs59619326
NM_002472.3(MYH8):c.3863-108CA[6] rs746761681
NM_002472.3(MYH8):c.387C>T (p.Asn129=) rs754559937
NM_002472.3(MYH8):c.405G>T (p.Pro135=) rs775704195
NM_002472.3(MYH8):c.4789G>A (p.Val1597Met)
NM_002472.3(MYH8):c.4962+10T>C rs749401636
NM_002472.3(MYH8):c.5115C>A (p.Ala1705=) rs200890789
NM_002472.3(MYH8):c.5166+229_5166+230dup rs35512526
NM_002472.3(MYH8):c.5166+249_5166+257del rs35512526
NM_002472.3(MYH8):c.5800A>G (p.Ile1934Val)

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