ClinVar Miner

List of variants in gene MYOM1 reported as likely benign for not specified

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Gene type:
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Total variants: 29
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HGVS dbSNP
NM_003803.3(MYOM1):c.1023-14G>A rs372359086
NM_003803.3(MYOM1):c.117C>T (p.Tyr39=) rs375113650
NM_003803.3(MYOM1):c.120C>G (p.Thr40=) rs876657535
NM_003803.3(MYOM1):c.1340-14delT rs554705715
NM_003803.3(MYOM1):c.1901-14T>C rs200115559
NM_003803.3(MYOM1):c.1917C>T (p.Gly639=) rs761762328
NM_003803.3(MYOM1):c.1952G>A (p.Arg651Gln) rs184721031
NM_003803.3(MYOM1):c.1978C>G (p.Pro660Ala) rs201104206
NM_003803.3(MYOM1):c.2062A>T (p.Thr688Ser) rs188677538
NM_003803.3(MYOM1):c.2064G>A (p.Thr688=) rs374462999
NM_003803.3(MYOM1):c.2350G>A (p.Glu784Lys) rs368949465
NM_003803.3(MYOM1):c.2385-13G>A rs116126674
NM_003803.3(MYOM1):c.2506+15C>G rs1272570164
NM_003803.3(MYOM1):c.2598G>A (p.Pro866=) rs778413922
NM_003803.3(MYOM1):c.2656A>G (p.Ser886Gly) rs199900004
NM_003803.3(MYOM1):c.2697A>C (p.Val899=) rs771666952
NM_003803.3(MYOM1):c.297A>G (p.Thr99=) rs369402806
NM_003803.3(MYOM1):c.3190C>T (p.His1064Tyr) rs755409090
NM_003803.3(MYOM1):c.3308G>A (p.Arg1103Gln) rs186972208
NM_003803.3(MYOM1):c.3539A>G (p.Asp1180Gly) rs188319622
NM_003803.3(MYOM1):c.3572A>G (p.Asn1191Ser) rs200480164
NM_003803.3(MYOM1):c.3683-9C>T rs1060504725
NM_003803.3(MYOM1):c.4648+7A>G rs555598943
NM_003803.3(MYOM1):c.4672T>C (p.Phe1558Leu) rs187108957
NM_003803.3(MYOM1):c.4776C>G (p.Leu1592=) rs1143658
NM_003803.3(MYOM1):c.5001G>A (p.Glu1667=) rs376007739
NM_003803.3(MYOM1):c.5045_5046insA (p.Lys1683Glufs) rs573184538
NM_003803.3(MYOM1):c.739G>A (p.Glu247Lys) rs139422575
NM_003803.3(MYOM1):c.93G>A (p.Arg31=) rs876657536

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