ClinVar Miner

List of variants in gene MYOM1 reported as benign by Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 52
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_003803.4(MYOM1):c.4069+13C>A rs948298 0.82097
NM_003803.4(MYOM1):c.4685+11G>T rs2298539 0.58772
NM_003803.4(MYOM1):c.5040T>C (p.Gly1680=) rs2230164 0.57606
NM_003803.4(MYOM1):c.3576-5C>T rs7232329 0.36941
NM_003803.4(MYOM1):c.541T>C (p.Ser181Pro) rs1962519 0.36782
NM_003803.4(MYOM1):c.1146C>T (p.His382=) rs2230163 0.33709
NM_003803.4(MYOM1):c.290+14C>G rs7232679 0.30460
NM_003803.4(MYOM1):c.999G>A (p.Gly333=) rs2230162 0.29399
NM_003803.4(MYOM1):c.1338C>T (p.Asn446=) rs2230167 0.27728
NM_003803.4(MYOM1):c.-9G>A rs1662315 0.26044
NM_003803.4(MYOM1):c.1392G>A (p.Arg464=) rs11659820 0.21420
NM_003803.4(MYOM1):c.2879T>C (p.Ile960Thr) rs1071600 0.19218
NM_003803.4(MYOM1):c.4662C>T (p.Ala1554=) rs1143657 0.18160
NM_003803.4(MYOM1):c.66G>C (p.Val22=) rs1662316 0.10760
NM_003803.4(MYOM1):c.660T>C (p.Ser220=) rs2230166 0.09353
NM_003803.4(MYOM1):c.644C>T (p.Thr215Met) rs2230165 0.07696
NM_003803.4(MYOM1):c.192G>T (p.Ala64=) rs9964300 0.06307
NM_003803.4(MYOM1):c.4222G>A (p.Asp1408Asn) rs3765623 0.05400
NM_003803.4(MYOM1):c.4358T>C (p.Met1453Thr) rs16944397 0.05084
NM_003803.4(MYOM1):c.1799A>T (p.Glu600Val) rs9807556 0.01756
NM_003803.4(MYOM1):c.2673G>C (p.Leu891=) rs115240600 0.01425
NM_003803.4(MYOM1):c.91C>A (p.Arg31=) rs76382984 0.01227
NM_003803.4(MYOM1):c.2210-4T>G rs143030509 0.01023
NM_003803.4(MYOM1):c.3945G>A (p.Thr1315=) rs75748615 0.00981
NM_003803.4(MYOM1):c.4069+4A>C rs80328493 0.00858
NM_003803.4(MYOM1):c.4718G>A (p.Arg1573Gln) rs117342470 0.00758
NM_003803.4(MYOM1):c.139A>G (p.Ser47Gly) rs202145133 0.00695
NM_003803.4(MYOM1):c.2110G>A (p.Glu704Lys) rs149528866 0.00679
NM_003803.4(MYOM1):c.539C>T (p.Thr180Ile) rs61735396 0.00612
NM_003803.4(MYOM1):c.3453T>A (p.Asp1151Glu) rs143879853 0.00578
NM_003803.4(MYOM1):c.1900+3A>C rs77613865 0.00536
NM_003803.4(MYOM1):c.1890G>A (p.Glu630=) rs36098676 0.00535
NM_003803.4(MYOM1):c.2179A>G (p.Thr727Ala) rs115382168 0.00345
NM_003803.4(MYOM1):c.1878T>C (p.Ile626=) rs180916932 0.00334
NM_003803.4(MYOM1):c.1843+10T>G rs116743447 0.00332
NM_003803.4(MYOM1):c.1455G>C (p.Arg485=) rs193006519 0.00323
NM_003803.4(MYOM1):c.1160C>T (p.Thr387Ile) rs189973743 0.00298
NM_003803.4(MYOM1):c.2384+4A>T rs73373171 0.00286
NM_003803.4(MYOM1):c.2802A>G (p.Pro934=) rs79397275 0.00222
NM_003803.4(MYOM1):c.461C>T (p.Thr154Met) rs140845661 0.00197
NM_003803.4(MYOM1):c.2727G>A (p.Pro909=) rs72860212 0.00188
NM_003803.4(MYOM1):c.1803C>T (p.Pro601=) rs371861150 0.00153
NM_003803.4(MYOM1):c.1112-11T>C rs59555146 0.00097
NM_003803.4(MYOM1):c.590C>T (p.Thr197Met) rs142735495 0.00050
NM_003803.4(MYOM1):c.1502-12C>T rs201937304 0.00024
NM_003803.4(MYOM1):c.3038C>T (p.Ala1013Val) rs557671408 0.00003
NM_003803.4(MYOM1):c.290G>T (p.Gly97Val) rs568600892 0.00001
NM_003803.4(MYOM1):c.1022G>C (p.Gly341Ala) rs8099021
NM_003803.4(MYOM1):c.2507-22TGT[2] rs147985558
NM_003803.4(MYOM1):c.3195C>G (p.Ser1065=) rs185366609
NM_003803.4(MYOM1):c.64G>C (p.Val22Leu) rs1791085
NM_003803.4(MYOM1):c.924C>A (p.Val308=) rs536739408

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.