ClinVar Miner

List of variants in gene MYOM1 reported as benign by Invitae

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Gene type:
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Total variants: 51
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HGVS dbSNP
NM_003803.3(MYOM1):c.1160C>T (p.Thr387Ile) rs189973743
NM_003803.3(MYOM1):c.117C>T (p.Tyr39=) rs375113650
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.1803C>T (p.Pro601=) rs371861150
NM_003803.3(MYOM1):c.1843+10T>G rs116743447
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.2062A>T (p.Thr688Ser) rs188677538
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.2181G>A (p.Thr727=) rs180910875
NM_003803.3(MYOM1):c.2210-4T>G rs143030509
NM_003803.3(MYOM1):c.2384+4A>T rs73373171
NM_003803.3(MYOM1):c.2469C>G (p.Ser823=) rs370860519
NM_003803.3(MYOM1):c.2625T>C (p.Leu875=) rs79149418
NM_003803.3(MYOM1):c.2673G>C (p.Leu891=) rs115240600
NM_003803.3(MYOM1):c.2715A>G (p.Glu905=) rs200170795
NM_003803.3(MYOM1):c.2727G>A (p.Pro909=) rs72860212
NM_003803.3(MYOM1):c.2802A>G (p.Pro934=) rs79397275
NM_003803.3(MYOM1):c.290G>T (p.Gly97Val) rs568600892
NM_003803.3(MYOM1):c.2991+8C>A rs138916150
NM_003803.3(MYOM1):c.3038C>T (p.Ala1013Val) rs557671408
NM_003803.3(MYOM1):c.3195C>G (p.Ser1065=) rs185366609
NM_003803.3(MYOM1):c.3207G>A (p.Pro1069=) rs367633441
NM_003803.3(MYOM1):c.3412C>T (p.Arg1138Cys) rs200710899
NM_003803.3(MYOM1):c.3453T>A (p.Asp1151Glu) rs143879853
NM_003803.3(MYOM1):c.3501C>T (p.Ser1167=) rs374054654
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.3639A>G (p.Thr1213=) rs558779097
NM_003803.3(MYOM1):c.3819C>T (p.Ala1273=) rs187236790
NM_003803.3(MYOM1):c.3945G>A (p.Thr1315=) rs75748615
NM_003803.3(MYOM1):c.4069+4A>C rs80328493
NM_003803.3(MYOM1):c.432-10_432-8delTGT rs770159154
NM_003803.3(MYOM1):c.4358T>C (p.Met1453Thr) rs16944397
NM_003803.3(MYOM1):c.45C>T (p.Leu15=) rs150321474
NM_003803.3(MYOM1):c.461C>T (p.Thr154Met) rs140845661
NM_003803.3(MYOM1):c.4648+9A>T rs758050936
NM_003803.3(MYOM1):c.4718G>A (p.Arg1573Gln) rs117342470
NM_003803.3(MYOM1):c.4764+10A>G rs79745437
NM_003803.3(MYOM1):c.4776C>G (p.Leu1592=) rs1143658
NM_003803.3(MYOM1):c.4961C>T (p.Ser1654Leu) rs199531701
NM_003803.3(MYOM1):c.5019C>T (p.Ala1673=) rs199980922
NM_003803.3(MYOM1):c.539C>T (p.Thr180Ile) rs61735396
NM_003803.3(MYOM1):c.590C>T (p.Thr197Met) rs142735495
NM_003803.3(MYOM1):c.684C>T (p.Ser228=) rs188155898
NM_003803.3(MYOM1):c.739G>A (p.Glu247Lys) rs139422575
NM_003803.3(MYOM1):c.91C>A (p.Arg31=) rs76382984

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