ClinVar Miner

List of variants in gene LMOD3 reported as likely benign for congenital myopathy

Included ClinVar conditions (289):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 84
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_198271.5(LMOD3):c.1190A>G (p.Gln397Arg) rs199592188 0.00163
NM_198271.5(LMOD3):c.1123T>C (p.Tyr375His) rs201506296 0.00057
NM_198271.5(LMOD3):c.927T>C (p.Asn309=) rs181434087 0.00056
NM_198271.5(LMOD3):c.416A>G (p.Asn139Ser) rs150380359 0.00053
NM_198271.5(LMOD3):c.1519G>A (p.Glu507Lys) rs149196259 0.00051
NM_198271.5(LMOD3):c.1667C>A (p.Pro556Gln) rs201205115 0.00023
NM_198271.5(LMOD3):c.1416A>G (p.Pro472=) rs563513367 0.00008
NM_198271.5(LMOD3):c.1585T>C (p.Leu529=) rs368819551 0.00008
NM_198271.5(LMOD3):c.1428G>A (p.Pro476=) rs367573665 0.00007
NM_198271.5(LMOD3):c.1518C>A (p.Pro506=) rs377380955 0.00007
NM_198271.5(LMOD3):c.1419G>A (p.Ser473=) rs373942606 0.00006
NM_198271.5(LMOD3):c.1492C>A (p.Arg498=) rs750486518 0.00006
NM_198271.5(LMOD3):c.1641C>G (p.Val547=) rs369854516 0.00006
NM_198271.5(LMOD3):c.375T>C (p.Asn125=) rs375595641 0.00006
NM_198271.5(LMOD3):c.438A>G (p.Glu146=) rs758216222 0.00006
NM_198271.5(LMOD3):c.1464G>A (p.Val488=) rs532434736 0.00005
NM_198271.5(LMOD3):c.1680G>A (p.Ala560=) rs377046368 0.00005
NM_198271.5(LMOD3):c.1335A>G (p.Glu445=) rs759597732 0.00004
NM_198271.5(LMOD3):c.1659G>T (p.Val553=) rs947092258 0.00004
NM_198271.5(LMOD3):c.608C>G (p.Pro203Arg) rs775919681 0.00004
NM_198271.5(LMOD3):c.1353A>G (p.Pro451=) rs756048205 0.00003
NM_198271.5(LMOD3):c.1500G>A (p.Pro500=) rs764693298 0.00003
NM_198271.5(LMOD3):c.744T>A (p.Val248=) rs1047754733 0.00003
NM_198271.5(LMOD3):c.778C>T (p.Leu260=) rs760458494 0.00003
NM_198271.5(LMOD3):c.819C>T (p.Asp273=) rs375767322 0.00003
NM_198271.5(LMOD3):c.987C>A (p.Ala329=) rs1367220865 0.00003
NM_198271.5(LMOD3):c.1350G>A (p.Pro450=) rs748774777 0.00002
NM_198271.5(LMOD3):c.1527C>T (p.Thr509=) rs746548821 0.00002
NM_198271.5(LMOD3):c.295-4G>A rs778291725 0.00002
NM_198271.5(LMOD3):c.906G>A (p.Leu302=) rs370070559 0.00002
NM_198271.5(LMOD3):c.1095G>A (p.Lys365=) rs185537696 0.00001
NM_198271.5(LMOD3):c.1246C>T (p.Leu416=) rs1440827868 0.00001
NM_198271.5(LMOD3):c.1377T>C (p.Asn459=) rs371736714 0.00001
NM_198271.5(LMOD3):c.1488A>G (p.Lys496=) rs756341632 0.00001
NM_198271.5(LMOD3):c.1579C>T (p.Pro527Ser) rs373480967 0.00001
NM_198271.5(LMOD3):c.295-5T>C rs747449404 0.00001
NM_198271.5(LMOD3):c.321A>G (p.Glu107=) rs754611563 0.00001
NM_198271.5(LMOD3):c.522A>G (p.Glu174=) rs777811015 0.00001
NM_198271.5(LMOD3):c.1011T>C (p.Asn337=)
NM_198271.5(LMOD3):c.1017G>A (p.Thr339=)
NM_198271.5(LMOD3):c.1056G>A (p.Leu352=)
NM_198271.5(LMOD3):c.1140G>A (p.Pro380=)
NM_198271.5(LMOD3):c.1158C>T (p.Val386=)
NM_198271.5(LMOD3):c.1200A>G (p.Lys400=) rs2107526132
NM_198271.5(LMOD3):c.1230C>G (p.Leu410=)
NM_198271.5(LMOD3):c.1230C>T (p.Leu410=)
NM_198271.5(LMOD3):c.1281C>G (p.Pro427=) rs1575879433
NM_198271.5(LMOD3):c.1296G>A (p.Glu432=)
NM_198271.5(LMOD3):c.1338C>T (p.Phe446=) rs771460251
NM_198271.5(LMOD3):c.1341C>T (p.Phe447=) rs747539477
NM_198271.5(LMOD3):c.1353A>C (p.Pro451=) rs756048205
NM_198271.5(LMOD3):c.1416A>T (p.Pro472=) rs563513367
NM_198271.5(LMOD3):c.1419G>T (p.Ser473=) rs373942606
NM_198271.5(LMOD3):c.1449C>T (p.Asp483=) rs2092390552
NM_198271.5(LMOD3):c.1455C>T (p.Phe485=) rs774967350
NM_198271.5(LMOD3):c.1533C>T (p.Leu511=)
NM_198271.5(LMOD3):c.1551G>T (p.Thr517=)
NM_198271.5(LMOD3):c.1566G>A (p.Pro522=)
NM_198271.5(LMOD3):c.1581C>T (p.Pro527=)
NM_198271.5(LMOD3):c.1641C>A (p.Val547=)
NM_198271.5(LMOD3):c.1656+9A>G
NM_198271.5(LMOD3):c.1680G>T (p.Ala560=)
NM_198271.5(LMOD3):c.295-14A>T
NM_198271.5(LMOD3):c.295-20C>G
NM_198271.5(LMOD3):c.312G>A (p.Glu104=)
NM_198271.5(LMOD3):c.369C>T (p.Leu123=) rs2092399816
NM_198271.5(LMOD3):c.417T>C (p.Asn139=) rs2107526866
NM_198271.5(LMOD3):c.435A>G (p.Glu145=) rs2107526854
NM_198271.5(LMOD3):c.444AGA[5] (p.Glu151dup) rs753459417
NM_198271.5(LMOD3):c.450A>G (p.Glu150=) rs1575881414
NM_198271.5(LMOD3):c.456TGA[3] (p.Asp157del) rs752238157
NM_198271.5(LMOD3):c.459T>C (p.Asp153=) rs557184030
NM_198271.5(LMOD3):c.465T>C (p.Asp155=)
NM_198271.5(LMOD3):c.468C>T (p.Asp156=)
NM_198271.5(LMOD3):c.471C>T (p.Asp157=) rs568706767
NM_198271.5(LMOD3):c.507G>A (p.Thr169=)
NM_198271.5(LMOD3):c.534G>A (p.Lys178=)
NM_198271.5(LMOD3):c.636A>G (p.Lys212=)
NM_198271.5(LMOD3):c.675C>G (p.Thr225=) rs1006337657
NM_198271.5(LMOD3):c.788T>C (p.Ile263Thr) rs9835034
NM_198271.5(LMOD3):c.843C>T (p.Asn281=) rs1268359340
NM_198271.5(LMOD3):c.861C>T (p.Phe287=)
NM_198271.5(LMOD3):c.870C>A (p.Ala290=)
NM_198271.5(LMOD3):c.990C>A (p.Ile330=)

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.