ClinVar Miner

List of variants in gene MYOM1 reported as benign by Ambry Genetics

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Gene type:
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Total variants: 32
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HGVS dbSNP
NM_003803.3(MYOM1):c.1022G>C (p.Gly341Ala) rs8099021
NM_003803.3(MYOM1):c.1146C>T (p.His382=) rs2230163
NM_003803.3(MYOM1):c.1338C>T (p.Asn446=) rs2230167
NM_003803.3(MYOM1):c.1392G>A (p.Arg464=) rs11659820
NM_003803.3(MYOM1):c.139A>G (p.Ser47Gly) rs202145133
NM_003803.3(MYOM1):c.1455G>C (p.Arg485=) rs193006519
NM_003803.3(MYOM1):c.1799A>T (p.Glu600Val) rs9807556
NM_003803.3(MYOM1):c.1878T>C (p.Ile626=) rs180916932
NM_003803.3(MYOM1):c.1890G>A (p.Glu630=) rs36098676
NM_003803.3(MYOM1):c.1900+3A>C rs77613865
NM_003803.3(MYOM1):c.192G>T (p.Ala64=) rs9964300
NM_003803.3(MYOM1):c.2110G>A (p.Glu704Lys) rs149528866
NM_003803.3(MYOM1):c.2179A>G (p.Thr727Ala) rs115382168
NM_003803.3(MYOM1):c.2210-4T>G rs143030509
NM_003803.3(MYOM1):c.2673G>C (p.Leu891=) rs115240600
NM_003803.3(MYOM1):c.2802A>G (p.Pro934=) rs79397275
NM_003803.3(MYOM1):c.2879T>C (p.Ile960Thr) rs1071600
NM_003803.3(MYOM1):c.3576-5C>T rs7232329
NM_003803.3(MYOM1):c.3945G>A (p.Thr1315=) rs75748615
NM_003803.3(MYOM1):c.4222G>A (p.Asp1408Asn) rs3765623
NM_003803.3(MYOM1):c.4358T>C (p.Met1453Thr) rs16944397
NM_003803.3(MYOM1):c.4662C>T (p.Ala1554=) rs1143657
NM_003803.3(MYOM1):c.4718G>A (p.Arg1573Gln) rs117342470
NM_003803.3(MYOM1):c.5040T>C (p.Gly1680=) rs2230164
NM_003803.3(MYOM1):c.539C>T (p.Thr180Ile) rs61735396
NM_003803.3(MYOM1):c.541T>C (p.Ser181Pro) rs1962519
NM_003803.3(MYOM1):c.644C>T (p.Thr215Met) rs2230165
NM_003803.3(MYOM1):c.64G>C (p.Val22Leu) rs1791085
NM_003803.3(MYOM1):c.660T>C (p.Ser220=) rs2230166
NM_003803.3(MYOM1):c.66G>C (p.Val22=) rs1662316
NM_003803.3(MYOM1):c.91C>A (p.Arg31=) rs76382984
NM_003803.3(MYOM1):c.999G>A (p.Gly333=) rs2230162

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