ClinVar Miner

List of variants in gene MYH7 reported as likely benign by Invitae

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 118
Download table as spreadsheet
HGVS dbSNP
NM_000257.4(MYH7):c.1000-7C>T rs200129563
NM_000257.4(MYH7):c.1020C>T (p.Gly340=) rs1301955127
NM_000257.4(MYH7):c.1083C>T (p.Asn361=) rs145091844
NM_000257.4(MYH7):c.1110G>A (p.Glu370=) rs1060504232
NM_000257.4(MYH7):c.1128C>A (p.Asp376Glu) rs2231126
NM_000257.4(MYH7):c.1191G>A (p.Lys397=) rs139506719
NM_000257.4(MYH7):c.1230C>T (p.Tyr410=) rs150885220
NM_000257.4(MYH7):c.1260G>A (p.Val420=) rs1555338342
NM_000257.4(MYH7):c.1266T>C (p.Tyr422=) rs141519877
NM_000257.4(MYH7):c.12G>A (p.Ser4=) rs45561941
NM_000257.4(MYH7):c.1322C>T (p.Thr441Met) rs121913653
NM_000257.4(MYH7):c.1323G>A (p.Thr441=) rs397516096
NM_000257.4(MYH7):c.1365C>T (p.Tyr455=) rs1025444130
NM_000257.4(MYH7):c.1408-8C>A rs764196309
NM_000257.4(MYH7):c.1482T>C (p.Phe494=) rs587781088
NM_000257.4(MYH7):c.1578+9T>G rs1339319984
NM_000257.4(MYH7):c.1579-4T>C rs1322757316
NM_000257.4(MYH7):c.1632C>T (p.Thr544=) rs587781089
NM_000257.4(MYH7):c.1668C>T (p.His556=) rs765643812
NM_000257.4(MYH7):c.1680C>T (p.Ser560=) rs763574368
NM_000257.4(MYH7):c.1749C>T (p.Ala583=) rs758665829
NM_000257.4(MYH7):c.1755C>A (p.Ile585=) rs201860580
NM_000257.4(MYH7):c.1755C>T (p.Ile585=) rs201860580
NM_000257.4(MYH7):c.183C>T (p.Ala61=) rs370743876
NM_000257.4(MYH7):c.1957-7G>A rs763943418
NM_000257.4(MYH7):c.2001C>G (p.Pro667=) rs748351798
NM_000257.4(MYH7):c.2028T>C (p.Asn676=) rs145564868
NM_000257.4(MYH7):c.2091T>C (p.Gly697=) rs140380523
NM_000257.4(MYH7):c.2162+9G>A rs765279420
NM_000257.4(MYH7):c.2184G>A (p.Ala728=) rs148650290
NM_000257.4(MYH7):c.2286+7A>G rs758365123
NM_000257.4(MYH7):c.2322G>A (p.Glu774=) rs1555337814
NM_000257.4(MYH7):c.2334C>T (p.Asp778=) rs2069544
NM_000257.4(MYH7):c.2349C>T (p.Arg783=) rs139882431
NM_000257.4(MYH7):c.2352C>T (p.Ile784=) rs397516143
NM_000257.4(MYH7):c.2360G>A (p.Arg787His) rs376754645
NM_000257.4(MYH7):c.240C>T (p.Asn80=) rs200493975
NM_000257.4(MYH7):c.2472C>T (p.Val824=) rs397516150
NM_000257.4(MYH7):c.2499C>T (p.Tyr833=) rs397516151
NM_000257.4(MYH7):c.2526T>C (p.Ser842=) rs554560162
NM_000257.4(MYH7):c.252C>T (p.Phe84=) rs267603955
NM_000257.4(MYH7):c.261C>T (p.Ile87=) rs148560996
NM_000257.4(MYH7):c.2679+7C>T rs368653983
NM_000257.4(MYH7):c.2859C>T (p.Asp953=) rs370800700
NM_000257.4(MYH7):c.2862C>T (p.Ile954=) rs982198020
NM_000257.4(MYH7):c.2868T>C (p.Asp956=) rs140718120
NM_000257.4(MYH7):c.28G>C (p.Gly10Arg) rs199577321
NM_000257.4(MYH7):c.2923-6C>T rs587781082
NM_000257.4(MYH7):c.2931C>T (p.Asn977=) rs757313728
NM_000257.4(MYH7):c.2945T>C (p.Met982Thr) rs145532615
NM_000257.4(MYH7):c.2988G>A (p.Lys996=) rs1176423898
NM_000257.4(MYH7):c.3245+7T>C rs995780485
NM_000257.4(MYH7):c.3246-8C>T rs1555337224
NM_000257.4(MYH7):c.3259C>T (p.Leu1087=) rs1299689855
NM_000257.4(MYH7):c.3273C>T (p.Asn1091=) rs200664031
NM_000257.4(MYH7):c.327C>T (p.Tyr109=) rs36211408
NM_000257.4(MYH7):c.3324C>T (p.Leu1108=) rs933857323
NM_000257.4(MYH7):c.3564T>C (p.Thr1188=) rs45587932
NM_000257.4(MYH7):c.3609G>T (p.Leu1203=) rs1555337108
NM_000257.4(MYH7):c.3618G>A (p.Gln1206=) rs1555337104
NM_000257.4(MYH7):c.3621C>T (p.Ile1207=) rs529700838
NM_000257.4(MYH7):c.3669G>A (p.Glu1223=) rs1023290989
NM_000257.4(MYH7):c.366T>C (p.Cys122=) rs1273010718
NM_000257.4(MYH7):c.3682C>T (p.Leu1228=) rs560995739
NM_000257.4(MYH7):c.36C>T (p.Ala12=) rs766884630
NM_000257.4(MYH7):c.3726+6C>T rs377745688
NM_000257.4(MYH7):c.3770A>G (p.Asn1257Ser) rs574005462
NM_000257.4(MYH7):c.3789G>A (p.Ala1263=) rs137918672
NM_000257.4(MYH7):c.3789G>T (p.Ala1263=) rs137918672
NM_000257.4(MYH7):c.3861G>C (p.Leu1287=) rs150292548
NM_000257.4(MYH7):c.3939G>A (p.Glu1313=) rs772128107
NM_000257.4(MYH7):c.3960G>A (p.Glu1320=) rs147797612
NM_000257.4(MYH7):c.396G>A (p.Pro132=) rs138932714
NM_000257.4(MYH7):c.3981C>A (p.Asn1327Lys) rs141764279
NM_000257.4(MYH7):c.4065C>T (p.Ala1355=) rs142469226
NM_000257.4(MYH7):c.4083T>G (p.Leu1361=) rs754295295
NM_000257.4(MYH7):c.4137C>T (p.Ala1379=) rs749048810
NM_000257.4(MYH7):c.4182C>T (p.Ala1394=) rs765895405
NM_000257.4(MYH7):c.4188G>A (p.Arg1396=) rs200852418
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.4239G>A (p.Ser1413=) rs3729821
NM_000257.4(MYH7):c.4251C>T (p.Thr1417=) rs763934978
NM_000257.4(MYH7):c.4257C>T (p.His1419=) rs1555336760
NM_000257.4(MYH7):c.474C>G (p.Ser158=) rs200444892
NM_000257.4(MYH7):c.503-4A>C rs376022200
NM_000257.4(MYH7):c.5253T>C (p.Ala1751=) rs776282574
NM_000257.4(MYH7):c.531C>T (p.Thr177=) rs200035152
NM_000257.4(MYH7):c.5361A>G (p.Glu1787=) rs201171029
NM_000257.4(MYH7):c.5400C>T (p.Ala1800=) rs556490774
NM_000257.4(MYH7):c.540C>A (p.Ser180=) rs369490861
NM_000257.4(MYH7):c.5412C>G (p.Ala1804=) rs147433856
NM_000257.4(MYH7):c.5421C>A (p.Gly1807=) rs142844109
NM_000257.4(MYH7):c.5421C>T (p.Gly1807=) rs142844109
NM_000257.4(MYH7):c.5451G>A (p.Ala1817=) rs138682220
NM_000257.4(MYH7):c.5481G>A (p.Glu1827=) rs368848344
NM_000257.4(MYH7):c.5541C>A (p.Ile1847=) rs770583523
NM_000257.4(MYH7):c.5560-7C>T rs778224065
NM_000257.4(MYH7):c.5562G>A (p.Thr1854=) rs368706722
NM_000257.4(MYH7):c.5574G>A (p.Arg1858=) rs529784690
NM_000257.4(MYH7):c.5601G>A (p.Leu1867=) rs1060504233
NM_000257.4(MYH7):c.5656-5C>T rs200231434
NM_000257.4(MYH7):c.5656-8dup rs886042307
NM_000257.4(MYH7):c.5661G>A (p.Glu1887=) rs730880727
NM_000257.4(MYH7):c.5664A>G (p.Gln1888=) rs540350007
NM_000257.4(MYH7):c.5704G>C (p.Glu1902Gln) rs187073962
NM_000257.4(MYH7):c.5718A>C (p.Ala1906=) rs45523233
NM_000257.4(MYH7):c.5730G>A (p.Ala1910=) rs776940948
NM_000257.4(MYH7):c.5761C>A (p.Arg1921=) rs539290591
NM_000257.4(MYH7):c.5790+9C>G rs1057521992
NM_000257.4(MYH7):c.633G>A (p.Pro211=) rs587781087
NM_000257.4(MYH7):c.639+9G>A rs373301620
NM_000257.4(MYH7):c.696T>C (p.Asn232=) rs1555338666
NM_000257.4(MYH7):c.78G>A (p.Ala26=) rs746119986
NM_000257.4(MYH7):c.796+7G>A rs369286647
NM_000257.4(MYH7):c.895+9G>C rs1555338571
NM_000257.4(MYH7):c.924C>T (p.Tyr308=) rs762065412
NM_000257.4(MYH7):c.957C>T (p.Thr319=) rs368699342

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.