List of variants reported as benign for Myopathy, distal, 1

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Total variants: 60

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HGVS	dbSNP
NM_000257.4(MYH7):c.*113G>A	rs17794387
NM_000257.4(MYH7):c.-36C>T	rs45497293
NM_000257.4(MYH7):c.-62C>T	rs45566639
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.1179C>T (p.Ala393=)	rs143293426
NM_000257.4(MYH7):c.1368C>T (p.Phe456=)	rs766216871
NM_000257.4(MYH7):c.1605A>G (p.Glu535=)	rs2069543
NM_000257.4(MYH7):c.1671G>T (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.2334C>T (p.Asp778=)	rs2069544
NM_000257.4(MYH7):c.240C>T (p.Asn80=)	rs200493975
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.2967T>C (p.Ile989=)	rs7157716
NM_000257.4(MYH7):c.297C>T (p.Pro99=)	rs140245862
NM_000257.4(MYH7):c.3036C>T (p.Ala1012=)	rs145379951
NM_000257.4(MYH7):c.3148C>A (p.Arg1050=)	rs730880767
NM_000257.4(MYH7):c.3153G>A (p.Ala1051=)	rs45540831
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.3351G>A (p.Glu1117=)	rs45554236
NM_000257.4(MYH7):c.350A>T (p.Tyr117Phe)	rs201012865
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.3853+7C>T	rs45467397
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.3972+15C>T	rs3729820
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.4188G>A (p.Arg1396=)	rs200852418
NM_000257.4(MYH7):c.4377G>T (p.Lys1459Asn)	rs201307101
NM_000257.4(MYH7):c.4410G>A (p.Ser1470=)	rs578166720
NM_000257.4(MYH7):c.4472C>G (p.Ser1491Cys)	rs3729823
NM_000257.4(MYH7):c.4557C>T (p.Ser1519=)	rs150552664
NM_000257.4(MYH7):c.4566T>C (p.Thr1522=)	rs2754155
NM_000257.4(MYH7):c.4659C>T (p.His1553=)	rs570079347
NM_000257.4(MYH7):c.4716C>T (p.Ile1572=)	rs7140196
NM_000257.4(MYH7):c.4806C>T (p.Asp1602=)	rs142034311
NM_000257.4(MYH7):c.480C>T (p.Asn160=)	rs45500700
NM_000257.4(MYH7):c.4872G>A (p.Glu1624=)
NM_000257.4(MYH7):c.5106G>A (p.Ala1702=)	rs3729830
NM_000257.4(MYH7):c.5243G>A (p.Cys1748Tyr)	rs200303340
NM_000257.4(MYH7):c.5394C>T (p.Asp1798=)	rs777053791
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.597A>G (p.Ala199=)	rs2069541
NM_000257.4(MYH7):c.732C>T (p.Phe244=)	rs2069542
NM_000257.4(MYH7):c.975C>T (p.Asp325=)	rs2231124
NM_000257.4(MYH7):c.976G>C (p.Ala326Pro)	rs372731424

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