ClinVar Miner

List of variants in gene MYH7 reported as likely benign for Myopathy, distal, 1

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Total variants: 28
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HGVS dbSNP
NM_000257.4(MYH7):c.*105T>C rs200550717
NM_000257.4(MYH7):c.*20G>A rs45548631
NM_000257.4(MYH7):c.1000-7C>T rs200129563
NM_000257.4(MYH7):c.1002C>T (p.Asn334=) rs34803781
NM_000257.4(MYH7):c.1191G>A (p.Lys397=) rs139506719
NM_000257.4(MYH7):c.153C>T (p.Ile51=) rs373145667
NM_000257.4(MYH7):c.2028T>C (p.Asn676=) rs145564868
NM_000257.4(MYH7):c.2349C>T (p.Arg783=) rs139882431
NM_000257.4(MYH7):c.2359C>T (p.Arg787Cys) rs145677314
NM_000257.4(MYH7):c.2360G>A (p.Arg787His) rs376754645
NM_000257.4(MYH7):c.2727C>A (p.Ile909=) rs377722048
NM_000257.4(MYH7):c.2765T>C (p.Met922Thr) rs771599539
NM_000257.4(MYH7):c.2769C>T (p.Asn923=) rs36211716
NM_000257.4(MYH7):c.2868T>C (p.Asp956=) rs140718120
NM_000257.4(MYH7):c.2890G>C (p.Val964Leu) rs45496496
NM_000257.4(MYH7):c.28G>C (p.Gly10Arg) rs199577321
NM_000257.4(MYH7):c.2945T>C (p.Met982Thr) rs145532615
NM_000257.4(MYH7):c.3035C>A (p.Ala1012Asp) rs779973529
NM_000257.4(MYH7):c.3156G>A (p.Lys1052=) rs138294643
NM_000257.4(MYH7):c.3235C>T (p.Arg1079Trp) rs192722540
NM_000257.4(MYH7):c.3337-4dup rs45504498
NM_000257.4(MYH7):c.3564T>C (p.Thr1188=) rs45587932
NM_000257.4(MYH7):c.3974C>T (p.Ala1325Val) rs768393069
NM_000257.4(MYH7):c.4227C>G (p.Ala1409=) rs148788346
NM_000257.4(MYH7):c.4239G>A (p.Ser1413=) rs3729821
NM_000257.4(MYH7):c.5704G>C (p.Glu1902Gln) rs187073962
NM_000257.4(MYH7):c.5718A>C (p.Ala1906=) rs45523233
NM_000257.4(MYH7):c.77C>T (p.Ala26Val) rs186964570

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