ClinVar Miner

List of variants in gene MYH7 reported as likely benign by Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 91
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HGVS dbSNP gnomAD frequency
NM_000257.4(MYH7):c.2162+4G>A rs145738465 0.00276
NM_000257.4(MYH7):c.4239G>A (p.Ser1413=) rs3729821 0.00267
NM_000257.4(MYH7):c.1395C>T (p.Phe465=) rs45508293 0.00082
NM_000257.4(MYH7):c.261C>T (p.Ile87=) rs148560996 0.00078
NM_000257.4(MYH7):c.4005G>A (p.Ser1335=) rs144465613 0.00064
NM_000257.4(MYH7):c.3156G>A (p.Lys1052=) rs138294643 0.00063
NM_000257.4(MYH7):c.3777C>T (p.His1259=) rs149103761 0.00054
NM_000257.4(MYH7):c.3036C>T (p.Ala1012=) rs145379951 0.00050
NM_000257.4(MYH7):c.2907C>T (p.His969=) rs142573531 0.00049
NM_000257.4(MYH7):c.3960G>A (p.Glu1320=) rs147797612 0.00044
NM_000257.4(MYH7):c.4188G>A (p.Arg1396=) rs200852418 0.00032
NM_000257.4(MYH7):c.3918C>T (p.Leu1306=) rs144420313 0.00030
NM_000257.4(MYH7):c.5725C>A (p.Arg1909=) rs146796870 0.00029
NM_000257.4(MYH7):c.77C>T (p.Ala26Val) rs186964570 0.00021
NM_000257.4(MYH7):c.796+7G>A rs369286647 0.00019
NM_000257.4(MYH7):c.5718A>C (p.Ala1906=) rs45523233 0.00016
NM_000257.4(MYH7):c.5562G>A (p.Thr1854=) rs368706722 0.00015
NM_000257.4(MYH7):c.3861G>C (p.Leu1287=) rs150292548 0.00014
NM_000257.4(MYH7):c.957C>T (p.Thr319=) rs368699342 0.00014
NM_000257.4(MYH7):c.3726+6C>T rs377745688 0.00013
NM_000257.4(MYH7):c.240C>T (p.Asn80=) rs200493975 0.00012
NM_000257.4(MYH7):c.3382G>A (p.Ala1128Thr) rs199552354 0.00011
NM_000257.4(MYH7):c.345C>T (p.Tyr115=) rs149439730 0.00011
NM_000257.4(MYH7):c.1191G>A (p.Lys397=) rs139506719 0.00010
NM_000257.4(MYH7):c.2091T>C (p.Gly697=) rs140380523 0.00009
NM_000257.4(MYH7):c.327C>T (p.Tyr109=) rs36211408 0.00009
NM_000257.4(MYH7):c.114C>T (p.Phe38=) rs146210693 0.00007
NM_000257.4(MYH7):c.5397A>G (p.Glu1799=) rs200374977 0.00007
NM_000257.4(MYH7):c.5499C>T (p.Asn1833=) rs3729831 0.00007
NM_000257.4(MYH7):c.1000-7C>T rs200129563 0.00006
NM_000257.4(MYH7):c.115G>A (p.Val39Met) rs376160714 0.00006
NM_000257.4(MYH7):c.1322C>T (p.Thr441Met) rs121913653 0.00006
NM_000257.4(MYH7):c.1888+8G>T rs200668471 0.00006
NM_000257.4(MYH7):c.2922G>A (p.Lys974=) rs147727900 0.00006
NM_000257.4(MYH7):c.4053G>A (p.Thr1351=) rs397516200 0.00006
NM_000257.4(MYH7):c.4182C>T (p.Ala1394=) rs765895405 0.00006
NM_000257.4(MYH7):c.474C>T (p.Ser158=) rs200444892 0.00006
NM_000257.4(MYH7):c.5559+8G>A rs377473156 0.00006
NM_000257.4(MYH7):c.1251C>G (p.Val417=) rs370628924 0.00005
NM_000257.4(MYH7):c.1323G>A (p.Thr441=) rs397516096 0.00005
NM_000257.4(MYH7):c.3273C>T (p.Asn1091=) rs200664031 0.00005
NM_000257.4(MYH7):c.12G>A (p.Ser4=) rs45561941 0.00004
NM_000257.4(MYH7):c.1332T>C (p.Asn444=) rs397516099 0.00004
NM_000257.4(MYH7):c.28G>C (p.Gly10Arg) rs199577321 0.00004
NM_000257.4(MYH7):c.3771T>C (p.Asn1257=) rs375219617 0.00004
NM_000257.4(MYH7):c.3993C>T (p.His1331=) rs200288088 0.00004
NM_000257.4(MYH7):c.4077C>T (p.Arg1359=) rs45523835 0.00004
NM_000257.4(MYH7):c.1608G>A (p.Glu536=) rs397516115 0.00003
NM_000257.4(MYH7):c.1983C>T (p.Asn661=) rs146474860 0.00003
NM_000257.4(MYH7):c.3337-10G>A rs397516181 0.00003
NM_000257.4(MYH7):c.3666C>T (p.Ser1222=) rs397516191 0.00003
NM_000257.4(MYH7):c.5656-5C>T rs200231434 0.00003
NM_000257.4(MYH7):c.733-9T>C rs944780538 0.00003
NM_000257.4(MYH7):c.895+12C>T rs186276057 0.00003
NM_000257.4(MYH7):c.1518C>T (p.Ile506=) rs397516108 0.00002
NM_000257.4(MYH7):c.2976G>A (p.Leu992=) rs368728770 0.00002
NM_000257.4(MYH7):c.3462C>T (p.Gly1154=) rs397516185 0.00002
NM_000257.4(MYH7):c.354G>A (p.Ser118=) rs368925624 0.00002
NM_000257.4(MYH7):c.5559+11C>T rs565014760 0.00002
NM_000257.4(MYH7):c.5559+9G>A rs727503241 0.00002
NM_000257.4(MYH7):c.1083C>T (p.Asn361=) rs145091844 0.00001
NM_000257.4(MYH7):c.1888+13T>G rs727504516 0.00001
NM_000257.4(MYH7):c.1926G>A (p.Ser642=) rs397516126 0.00001
NM_000257.4(MYH7):c.2229G>A (p.Glu743=) rs397516139 0.00001
NM_000257.4(MYH7):c.2979C>T (p.Thr993=) rs397516176 0.00001
NM_000257.4(MYH7):c.4227C>G (p.Ala1409=) rs148788346 0.00001
NM_000257.4(MYH7):c.5703C>T (p.His1901=) rs45570635 0.00001
NM_000257.4(MYH7):c.5787G>A (p.Thr1929=) rs397516257 0.00001
NM_000257.4(MYH7):c.1269C>T (p.Ala423=) rs727503267
NM_000257.4(MYH7):c.1536C>T (p.Asp512=) rs1555338248
NM_000257.4(MYH7):c.156G>A (p.Val52=) rs397516112
NM_000257.4(MYH7):c.1653G>A (p.Lys551=) rs368160680
NM_000257.4(MYH7):c.1755C>A (p.Ile585=) rs201860580
NM_000257.4(MYH7):c.183C>G (p.Ala61=) rs370743876
NM_000257.4(MYH7):c.2052G>A (p.Met684Ile) rs727503262
NM_000257.4(MYH7):c.2799T>C (p.Asn933=) rs397516173
NM_000257.4(MYH7):c.2802T>G (p.Ala934=) rs397516174
NM_000257.4(MYH7):c.2823C>T (p.Arg941=) rs727503251
NM_000257.4(MYH7):c.3438C>T (p.Ile1146=) rs876657519
NM_000257.4(MYH7):c.3621C>A (p.Ile1207=) rs529700838
NM_000257.4(MYH7):c.3754T>C (p.Leu1252=) rs397516193
NM_000257.4(MYH7):c.3829C>A (p.Arg1277=) rs727503248
NM_000257.4(MYH7):c.396G>T (p.Pro132=) rs138932714
NM_000257.4(MYH7):c.3981C>A (p.Asn1327Lys) rs141764279
NM_000257.4(MYH7):c.4188G>T (p.Arg1396=) rs200852418
NM_000257.4(MYH7):c.4212G>T (p.Val1404=) rs397516205
NM_000257.4(MYH7):c.5421C>G (p.Gly1807=) rs142844109
NM_000257.4(MYH7):c.5421C>T (p.Gly1807=) rs142844109
NM_000257.4(MYH7):c.5656-4G>C rs397516250
NM_000257.4(MYH7):c.5739C>T (p.Ala1913=) rs200921000
NM_000257.4(MYH7):c.895+11G>A rs727504860

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