ClinVar Miner

List of variants in gene MYH7 reported by Illumina Clinical Services Laboratory,Illumina

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 79
Download table as spreadsheet
HGVS dbSNP
NM_000257.2(MYH7):c.5482G>A (p.Ala1828Thr) rs886050415
NM_000257.2(MYH7):c.5726G>A (p.Arg1909Gln) rs397516253
NM_000257.3(MYH7):c.*105T>C rs200550717
NM_000257.3(MYH7):c.*20G>A rs45548631
NM_000257.3(MYH7):c.-36C>T rs45497293
NM_000257.3(MYH7):c.-39C>A rs886050424
NM_000257.3(MYH7):c.-47G>T rs886050425
NM_000257.3(MYH7):c.-62C>T rs45566639
NM_000257.3(MYH7):c.1000-13G>T rs772831757
NM_000257.3(MYH7):c.1000-7C>T rs200129563
NM_000257.3(MYH7):c.1138+7G>A rs886050423
NM_000257.3(MYH7):c.1139-4C>T rs886050422
NM_000257.3(MYH7):c.1179C>T (p.Ala393=) rs143293426
NM_000257.3(MYH7):c.1191G>A (p.Lys397=) rs139506719
NM_000257.3(MYH7):c.153C>T (p.Ile51=) rs373145667
NM_000257.3(MYH7):c.1671G>T (p.Leu557=) rs149386750
NM_000257.3(MYH7):c.1749C>T (p.Ala583=) rs758665829
NM_000257.3(MYH7):c.1755C>A (p.Ile585=) rs201860580
NM_000257.3(MYH7):c.1888+8G>T rs200668471
NM_000257.3(MYH7):c.1983C>T (p.Asn661=) rs146474860
NM_000257.3(MYH7):c.2028T>C (p.Asn676=) rs145564868
NM_000257.3(MYH7):c.2349C>T (p.Arg783=) rs139882431
NM_000257.3(MYH7):c.2526T>C (p.Ser842=) rs554560162
NM_000257.3(MYH7):c.2692C>T (p.Leu898=) rs727504407
NM_000257.3(MYH7):c.2727C>A (p.Ile909=) rs377722048
NM_000257.3(MYH7):c.2890G>C (p.Val964Leu) rs45496496
NM_000257.3(MYH7):c.2922+6G>C rs781192476
NM_000257.3(MYH7):c.2936C>G (p.Thr979Arg) rs886050421
NM_000257.3(MYH7):c.2955G>A (p.Leu985=) rs886050420
NM_000257.3(MYH7):c.2968G>A (p.Ala990Thr) rs753137666
NM_000257.3(MYH7):c.3148C>A (p.Arg1050=) rs730880767
NM_000257.3(MYH7):c.3235C>T (p.Arg1079Trp) rs192722540
NM_000257.3(MYH7):c.3564T>C (p.Thr1188=) rs45587932
NM_000257.3(MYH7):c.3621C>T (p.Ile1207=) rs529700838
NM_000257.3(MYH7):c.3934C>T (p.Leu1312=) rs886050419
NM_000257.3(MYH7):c.3972+15C>T rs3729820
NM_000257.3(MYH7):c.3974C>T (p.Ala1325Val) rs768393069
NM_000257.3(MYH7):c.4158C>T (p.Leu1386=) rs886050418
NM_000257.3(MYH7):c.4169+6T>G rs886050417
NM_000257.3(MYH7):c.4188G>A (p.Arg1396=) rs200852418
NM_000257.3(MYH7):c.4239G>A (p.Ser1413=) rs3729821
NM_000257.3(MYH7):c.449C>G (p.Ala150Gly) rs879196018
NM_000257.3(MYH7):c.540C>A (p.Ser180=) rs369490861
NM_000257.3(MYH7):c.5499C>T (p.Asn1833=) rs3729831
NM_000257.3(MYH7):c.5606A>G (p.Asp1869Gly) rs730880824
NM_000257.3(MYH7):c.5718A>C (p.Ala1906=) rs45523233
NM_000257.3(MYH7):c.658A>C (p.Ile220Leu) rs779190577
NM_000257.3(MYH7):c.733-3C>T rs765068619
NM_000257.3(MYH7):c.895+12C>A rs186276057
NM_000257.3(MYH7):c.976G>C (p.Ala326Pro) rs372731424
NM_000257.4(MYH7):c.1002C>T (p.Asn334=) rs34803781
NM_000257.4(MYH7):c.1062C>T (p.Gly354=) rs735712
NM_000257.4(MYH7):c.1095G>A (p.Lys365=) rs735711
NM_000257.4(MYH7):c.1119G>A (p.Ala373=) rs572672362
NM_000257.4(MYH7):c.1128C>T (p.Asp376=) rs2231126
NM_000257.4(MYH7):c.1605A>G (p.Glu535=) rs2069543
NM_000257.4(MYH7):c.1767C>T (p.Asn589=) rs3729816
NM_000257.4(MYH7):c.189C>T (p.Thr63=) rs2069540
NM_000257.4(MYH7):c.2360G>A (p.Arg787His) rs376754645
NM_000257.4(MYH7):c.2769C>T (p.Asn923=) rs36211716
NM_000257.4(MYH7):c.2945T>C (p.Met982Thr) rs145532615
NM_000257.4(MYH7):c.2967T>C (p.Ile989=) rs7157716
NM_000257.4(MYH7):c.297C>T (p.Pro99=) rs140245862
NM_000257.4(MYH7):c.3035C>A (p.Ala1012Asp) rs779973529
NM_000257.4(MYH7):c.3036C>T (p.Ala1012=) rs145379951
NM_000257.4(MYH7):c.3153G>A (p.Ala1051=) rs45540831
NM_000257.4(MYH7):c.3156G>A (p.Lys1052=) rs138294643
NM_000257.4(MYH7):c.3337-3dup rs45504498
NM_000257.4(MYH7):c.3351G>A (p.Glu1117=) rs45554236
NM_000257.4(MYH7):c.3770A>G (p.Asn1257Ser) rs574005462
NM_000257.4(MYH7):c.3853+7C>T rs45467397
NM_000257.4(MYH7):c.3918C>T (p.Leu1306=) rs144420313
NM_000257.4(MYH7):c.480C>T (p.Asn160=) rs45500700
NM_000257.4(MYH7):c.5394C>T (p.Asp1798=) rs777053791
NM_000257.4(MYH7):c.5704G>C (p.Glu1902Gln) rs187073962
NM_000257.4(MYH7):c.597A>G (p.Ala199=) rs2069541
NM_000257.4(MYH7):c.732C>T (p.Phe244=) rs2069542
NM_000257.4(MYH7):c.77C>T (p.Ala26Val) rs186964570
NM_000257.4(MYH7):c.975C>T (p.Asp325=) rs2231124

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.