ClinVar Miner

List of variants in gene MYH7 reported as uncertain significance for Myosin storage myopathy

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Gene type:
ClinVar version:
Total variants: 82
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HGVS dbSNP
NM_000257.4(MYH7):c.*81G>A
NM_000257.4(MYH7):c.-39C>A rs886050424
NM_000257.4(MYH7):c.-47G>T rs886050425
NM_000257.4(MYH7):c.-62C>T rs45566639
NM_000257.4(MYH7):c.1000-13G>T rs772831757
NM_000257.4(MYH7):c.1119G>A (p.Ala373=) rs572672362
NM_000257.4(MYH7):c.1138+7G>A rs886050423
NM_000257.4(MYH7):c.1139-4C>T rs886050422
NM_000257.4(MYH7):c.1179C>T (p.Ala393=) rs143293426
NM_000257.4(MYH7):c.1191G>A (p.Lys397=) rs139506719
NM_000257.4(MYH7):c.1334C>T (p.Ala445Val) rs752349938
NM_000257.4(MYH7):c.1368C>T (p.Phe456=) rs766216871
NM_000257.4(MYH7):c.1671G>T (p.Leu557=) rs149386750
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.1888+8G>T rs200668471
NM_000257.4(MYH7):c.1983C>T (p.Asn661=) rs146474860
NM_000257.4(MYH7):c.2028T>C (p.Asn676=) rs145564868
NM_000257.4(MYH7):c.2168G>A (p.Arg723His) rs397516135
NM_000257.4(MYH7):c.2334C>T (p.Asp778=) rs2069544
NM_000257.4(MYH7):c.240C>T (p.Asn80=) rs200493975
NM_000257.4(MYH7):c.2424-7C>T
NM_000257.4(MYH7):c.2526T>C (p.Ser842=) rs554560162
NM_000257.4(MYH7):c.2692C>T (p.Leu898=) rs727504407
NM_000257.4(MYH7):c.2765T>C (p.Met922Thr) rs771599539
NM_000257.4(MYH7):c.2868T>C (p.Asp956=) rs140718120
NM_000257.4(MYH7):c.2877G>A (p.Leu959=) rs886039162
NM_000257.4(MYH7):c.28G>C (p.Gly10Arg) rs199577321
NM_000257.4(MYH7):c.2922+6G>C rs781192476
NM_000257.4(MYH7):c.2936C>G (p.Thr979Arg) rs886050421
NM_000257.4(MYH7):c.2955G>A (p.Leu985=) rs886050420
NM_000257.4(MYH7):c.2968G>A (p.Ala990Thr) rs753137666
NM_000257.4(MYH7):c.2981A>G (p.Lys994Arg)
NM_000257.4(MYH7):c.3030T>G (p.Leu1010=)
NM_000257.4(MYH7):c.3035C>A (p.Ala1012Asp) rs779973529
NM_000257.4(MYH7):c.3110C>A (p.Ser1037Tyr)
NM_000257.4(MYH7):c.3148C>A (p.Arg1050=) rs730880767
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.350A>T (p.Tyr117Phe) rs201012865
NM_000257.4(MYH7):c.3558G>A (p.Glu1186=)
NM_000257.4(MYH7):c.3621C>T (p.Ile1207=) rs529700838
NM_000257.4(MYH7):c.3690C>T (p.Asp1230=) rs370750044
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>T (p.Ala1263=) rs137918672
NM_000257.4(MYH7):c.3801G>C (p.Gln1267His) rs200000290
NM_000257.4(MYH7):c.3934C>T (p.Leu1312=) rs886050419
NM_000257.4(MYH7):c.3960G>A (p.Glu1320=) rs147797612
NM_000257.4(MYH7):c.3974C>T (p.Ala1325Val) rs768393069
NM_000257.4(MYH7):c.3981C>A (p.Asn1327Lys) rs141764279
NM_000257.4(MYH7):c.4134C>T (p.Asp1378=) rs770630028
NM_000257.4(MYH7):c.4144C>T (p.Arg1382Trp) rs730880910
NM_000257.4(MYH7):c.4158C>T (p.Leu1386=) rs886050418
NM_000257.4(MYH7):c.4159G>A (p.Glu1387Lys) rs730880792
NM_000257.4(MYH7):c.4169+6T>G rs886050417
NM_000257.4(MYH7):c.4187G>A (p.Arg1396Gln) rs370069461
NM_000257.4(MYH7):c.4188G>A (p.Arg1396=) rs200852418
NM_000257.4(MYH7):c.4227C>G (p.Ala1409=) rs148788346
NM_000257.4(MYH7):c.449C>G (p.Ala150Gly) rs879196018
NM_000257.4(MYH7):c.5243G>A (p.Cys1748Tyr) rs200303340
NM_000257.4(MYH7):c.5279C>T (p.Thr1760Met) rs727505294
NM_000257.4(MYH7):c.5287G>A (p.Ala1763Thr) rs727504355
NM_000257.4(MYH7):c.5394C>T (p.Asp1798=) rs777053791
NM_000257.4(MYH7):c.540C>A (p.Ser180=) rs369490861
NM_000257.4(MYH7):c.5482G>A (p.Ala1828Thr) rs886050415
NM_000257.4(MYH7):c.5499C>T (p.Asn1833=) rs3729831
NM_000257.4(MYH7):c.5500G>A (p.Ala1834Thr) rs143362532
NM_000257.4(MYH7):c.5507C>T (p.Ser1836Leu) rs727503242
NM_000257.4(MYH7):c.5606A>G (p.Asp1869Gly) rs730880824
NM_000257.4(MYH7):c.5718A>C (p.Ala1906=) rs45523233
NM_000257.4(MYH7):c.5725C>T (p.Arg1909Trp)
NM_000257.4(MYH7):c.5726G>A (p.Arg1909Gln) rs397516253
NM_000257.4(MYH7):c.5787G>A (p.Thr1929=) rs397516257
NM_000257.4(MYH7):c.5793C>T (p.Gly1931=)
NM_000257.4(MYH7):c.639+13C>T
NM_000257.4(MYH7):c.658A>C (p.Ile220Leu) rs779190577
NM_000257.4(MYH7):c.733-3C>T rs765068619
NM_000257.4(MYH7):c.745C>G (p.Arg249Gly) rs730880852
NM_000257.4(MYH7):c.801T>C (p.Leu267=) rs1171861442
NM_000257.4(MYH7):c.895+12C>A rs186276057
NM_000257.4(MYH7):c.976G>C (p.Ala326Pro) rs372731424

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