ClinVar Miner

List of variants in gene MYH7 reported by Color

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 101
Download table as spreadsheet
HGVS dbSNP
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.1065C>T (p.Ala355=) rs778136999
NM_000257.4(MYH7):c.1095G>A (p.Lys365=) rs735711
NM_000257.4(MYH7):c.1128C>T (p.Asp376=) rs2231126
NM_000257.4(MYH7):c.1139-14C>T rs397516091
NM_000257.4(MYH7):c.1191G>A (p.Lys397=) rs139506719
NM_000257.4(MYH7):c.1322C>T (p.Thr441Met) rs121913653
NM_000257.4(MYH7):c.1534G>A (p.Asp512Asn) rs1566534648
NM_000257.4(MYH7):c.1605A>G (p.Glu535=) rs2069543
NM_000257.4(MYH7):c.1671G>A (p.Leu557=) rs149386750
NM_000257.4(MYH7):c.1755C>A (p.Ile585=) rs201860580
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.2041C>T (p.Pro681Ser) rs1566533236
NM_000257.4(MYH7):c.2162+4G>A rs145738465
NM_000257.4(MYH7):c.2301C>T (p.Ala767=) rs768380939
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.2360G>A (p.Arg787His) rs376754645
NM_000257.4(MYH7):c.240C>T (p.Asn80=) rs200493975
NM_000257.4(MYH7):c.2514G>A (p.Pro838=) rs45560638
NM_000257.4(MYH7):c.2525G>C (p.Ser842Thr) rs397516154
NM_000257.4(MYH7):c.2526T>C (p.Ser842=) rs554560162
NM_000257.4(MYH7):c.2553C>A (p.Ser851=) rs144291282
NM_000257.4(MYH7):c.2769C>T (p.Asn923=) rs36211716
NM_000257.4(MYH7):c.2890G>C (p.Val964Leu) rs45496496
NM_000257.4(MYH7):c.2923-6C>T rs587781082
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.300G>A (p.Ala100=) rs757141502
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.3068C>T (p.Ala1023Val) rs767004235
NM_000257.4(MYH7):c.3100-15C>T rs534114622
NM_000257.4(MYH7):c.3138G>A (p.Met1046Ile) rs201195256
NM_000257.4(MYH7):c.3153G>A (p.Ala1051=) rs45540831
NM_000257.4(MYH7):c.3235C>T (p.Arg1079Trp) rs192722540
NM_000257.4(MYH7):c.327C>T (p.Tyr109=) rs36211408
NM_000257.4(MYH7):c.3286G>T (p.Asp1096Tyr) rs45478699
NM_000257.4(MYH7):c.3337-4dup rs45504498
NM_000257.4(MYH7):c.3351G>A (p.Glu1117=) rs45554236
NM_000257.4(MYH7):c.3372C>T (p.Ala1124=) rs1372163543
NM_000257.4(MYH7):c.3382G>A (p.Ala1128Thr) rs199552354
NM_000257.4(MYH7):c.3387G>A (p.Arg1129=) rs1566528000
NM_000257.4(MYH7):c.3402G>A (p.Lys1134=) rs587781083
NM_000257.4(MYH7):c.3414C>T (p.Asp1138=) rs1566527962
NM_000257.4(MYH7):c.3422G>A (p.Arg1141Gln) rs1407919500
NM_000257.4(MYH7):c.3432G>A (p.Glu1144=) rs552605072
NM_000257.4(MYH7):c.3451G>C (p.Glu1151Gln) rs1370927693
NM_000257.4(MYH7):c.3460G>A (p.Gly1154Ser) rs1211784451
NM_000257.4(MYH7):c.3474C>T (p.Ser1158=) rs587780395
NM_000257.4(MYH7):c.3483C>G (p.Ile1161Met) rs778909719
NM_000257.4(MYH7):c.3502G>A (p.Glu1168Lys) rs1566527832
NM_000257.4(MYH7):c.354G>A (p.Ser118=) rs368925624
NM_000257.4(MYH7):c.3555C>T (p.His1185=) rs1387218063
NM_000257.4(MYH7):c.3563C>T (p.Thr1188Ile) rs1566527771
NM_000257.4(MYH7):c.3567C>T (p.Ala1189=) rs1165812799
NM_000257.4(MYH7):c.3592G>A (p.Asp1198Asn) rs730880778
NM_000257.4(MYH7):c.3598G>A (p.Val1200Met) rs375283149
NM_000257.4(MYH7):c.3603C>G (p.Ala1201=) rs201576345
NM_000257.4(MYH7):c.3609G>T (p.Leu1203=) rs1555337108
NM_000257.4(MYH7):c.3621C>T (p.Ile1207=) rs529700838
NM_000257.4(MYH7):c.3682C>T (p.Leu1228=) rs560995739
NM_000257.4(MYH7):c.372C>T (p.Thr124=) rs755855267
NM_000257.4(MYH7):c.3770A>G (p.Asn1257Ser) rs574005462
NM_000257.4(MYH7):c.3783C>G (p.Ser1261Arg) rs1566527289
NM_000257.4(MYH7):c.3803G>A (p.Arg1268His) rs397516194
NM_000257.4(MYH7):c.3861G>C (p.Leu1287=) rs150292548
NM_000257.4(MYH7):c.3918C>T (p.Leu1306=) rs144420313
NM_000257.4(MYH7):c.3960G>A (p.Glu1320=) rs147797612
NM_000257.4(MYH7):c.3981C>A (p.Asn1327Lys) rs141764279
NM_000257.4(MYH7):c.3993C>T (p.His1331=) rs200288088
NM_000257.4(MYH7):c.4010G>A (p.Arg1337Gln) rs368575559
NM_000257.4(MYH7):c.4041C>T (p.Tyr1347=) rs1199930760
NM_000257.4(MYH7):c.4063G>A (p.Ala1355Thr) rs755058300
NM_000257.4(MYH7):c.4066G>A (p.Glu1356Lys) rs727503246
NM_000257.4(MYH7):c.4210G>A (p.Val1404Met) rs371552806
NM_000257.4(MYH7):c.4239G>A (p.Ser1413=) rs3729821
NM_000257.4(MYH7):c.480C>T (p.Asn160=) rs45500700
NM_000257.4(MYH7):c.5253T>C (p.Ala1751=) rs776282574
NM_000257.4(MYH7):c.5361A>G (p.Glu1787=) rs201171029
NM_000257.4(MYH7):c.5394C>T (p.Asp1798=) rs777053791
NM_000257.4(MYH7):c.5400C>T (p.Ala1800=) rs556490774
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.5484C>T (p.Ala1828=) rs202175645
NM_000257.4(MYH7):c.5560-14C>A rs375621171
NM_000257.4(MYH7):c.5562G>A (p.Thr1854=) rs368706722
NM_000257.4(MYH7):c.5656-4G>A rs397516250
NM_000257.4(MYH7):c.5736C>T (p.Ile1912=) rs200728597
NM_000257.4(MYH7):c.5786C>T (p.Thr1929Met) rs730880918
NM_000257.4(MYH7):c.597A>G (p.Ala199=) rs2069541
NM_000257.4(MYH7):c.633G>A (p.Pro211=) rs587781087
NM_000257.4(MYH7):c.67C>T (p.Arg23Trp) rs730880828
NM_000257.4(MYH7):c.705C>T (p.Thr235=) rs552415639
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.957C>T (p.Thr319=) rs368699342
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.