ClinVar Miner

List of variants in gene MYH7 reported as uncertain significance for Myopathy, distal, 1

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Total variants: 43
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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.1000-13G>T rs772831757
NM_000257.4(MYH7):c.1138+7G>A rs886050423
NM_000257.4(MYH7):c.1139-4C>T rs886050422
NM_000257.4(MYH7):c.1334C>T (p.Ala445Val) rs752349938
NM_000257.4(MYH7):c.1749C>T (p.Ala583=) rs758665829
NM_000257.4(MYH7):c.1888+8G>T rs200668471
NM_000257.4(MYH7):c.1983C>T (p.Asn661=) rs146474860
NM_000257.4(MYH7):c.2080C>T (p.Arg694Cys) rs727504240
NM_000257.4(MYH7):c.2168G>A (p.Arg723His) rs397516135
NM_000257.4(MYH7):c.2424-7C>T
NM_000257.4(MYH7):c.2877G>A (p.Leu959=) rs886039162
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.3110C>A (p.Ser1037Tyr)
NM_000257.4(MYH7):c.3558G>A (p.Glu1186=)
NM_000257.4(MYH7):c.3934C>T (p.Leu1312=) rs886050419
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.449C>G (p.Ala150Gly) rs879196018
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.540C>A (p.Ser180=) rs369490861
NM_000257.4(MYH7):c.5482G>A (p.Ala1828Thr) rs886050415
NM_000257.4(MYH7):c.5606A>G (p.Asp1869Gly) rs730880824
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

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