ClinVar Miner

List of variants in gene LMOD3 reported as likely benign for hereditary skeletal muscle disorder

Included ClinVar conditions (591):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 95
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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.1002C>T (p.Leu334=)
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.1155G>T (p.Val385=)
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.1410A>G (p.Lys470=)
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.1458G>C (p.Arg486=)
NM_198271.5(LMOD3):c.1533C>T (p.Leu511=)
NM_198271.5(LMOD3):c.1551G>A (p.Thr517=)
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+12G>T
NM_198271.5(LMOD3):c.1656+9A>G
NM_198271.5(LMOD3):c.1656+9_1656+11del
NM_198271.5(LMOD3):c.1662A>G (p.Gln554=)
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.543T>A (p.Ile181=)
NM_198271.5(LMOD3):c.636A>G (p.Lys212=)
NM_198271.5(LMOD3):c.642G>T (p.Ser214=)
NM_198271.5(LMOD3):c.675C>G (p.Thr225=) rs1006337657
NM_198271.5(LMOD3):c.720C>T (p.Asp240=)
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=)

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