ClinVar Miner

List of variants in gene DMD reported as likely benign by EGL Genetic Diagnostics,Eurofins Clinical Diagnostics

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Gene type:
ClinVar version:
Total variants: 49
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HGVS dbSNP
NM_004006.2(DMD):c.-188del rs886042325
NM_004006.2(DMD):c.1028G>A (p.Arg343His) rs61733589
NM_004006.2(DMD):c.1059G>A (p.Ser353=) rs760621626
NM_004006.2(DMD):c.10836C>T (p.Ser3612=) rs148590546
NM_004006.2(DMD):c.1184G>A (p.Arg395Gln) rs148511512
NM_004006.2(DMD):c.1252A>T (p.Thr418Ser) rs201341211
NM_004006.2(DMD):c.1813-3C>A rs181399181
NM_004006.2(DMD):c.1869C>G (p.Leu623=) rs1800267
NM_004006.2(DMD):c.1934A>G (p.Asp645Gly) rs147822019
NM_004006.2(DMD):c.2380+10C>T rs372330460
NM_004006.2(DMD):c.2569C>T (p.Pro857Ser) rs552275776
NM_004006.2(DMD):c.2575A>T (p.Thr859Ser) rs187926894
NM_004006.2(DMD):c.2745A>C (p.Thr915=) rs149922633
NM_004006.2(DMD):c.2884C>G (p.Leu962Val) rs150959827
NM_004006.2(DMD):c.2971G>C (p.Glu991Gln) rs72468667
NM_004006.2(DMD):c.3020C>T (p.Ser1007Leu) rs144732570
NM_004006.2(DMD):c.3432+2036A>C rs182575709
NM_004006.2(DMD):c.3603+15dupA rs5902031
NM_004006.2(DMD):c.3635C>T (p.Ala1212Val) rs142171890
NM_004006.2(DMD):c.3666T>C (p.Asn1222=) rs373281760
NM_004006.2(DMD):c.3794G>C (p.Trp1265Ser) rs200213555
NM_004006.2(DMD):c.3970C>T (p.Arg1324Cys) rs143184877
NM_004006.2(DMD):c.4093C>T (p.Leu1365Phe) rs148781346
NM_004006.2(DMD):c.4125T>C (p.Thr1375=) rs144329742
NM_004006.2(DMD):c.4233+2C>T rs147474070
NM_004006.2(DMD):c.4876G>A (p.Val1626Met) rs776998846
NM_004006.2(DMD):c.5182C>T (p.Arg1728Cys) rs34102501
NM_004006.2(DMD):c.5203C>T (p.Arg1735Cys) rs147904018
NM_004006.2(DMD):c.5265C>T (p.Pro1755=) rs145515413
NM_004006.2(DMD):c.5485C>G (p.Gln1829Glu) rs754765424
NM_004006.2(DMD):c.5586+9G>A rs200025478
NM_004006.2(DMD):c.5620G>A (p.Glu1874Lys) rs142441725
NM_004006.2(DMD):c.5701G>A (p.Ala1901Thr) rs201302282
NM_004006.2(DMD):c.5723A>T (p.Asp1908Val) rs145266970
NM_004006.2(DMD):c.6614+8G>A rs377508818
NM_004006.2(DMD):c.6732G>C (p.Gln2244His) rs142531761
NM_004006.2(DMD):c.696C>G (p.Ile232Met) rs145668843
NM_004006.2(DMD):c.7016A>G (p.His2339Arg) rs398124041
NM_004006.2(DMD):c.7310-7A>G rs373230021
NM_004006.2(DMD):c.7472A>G (p.Gln2491Arg) rs147694734
NM_004006.2(DMD):c.7571G>A (p.Arg2524His) rs151244052
NM_004006.2(DMD):c.7653G>A (p.Thr2551=) rs368803197
NM_004006.2(DMD):c.8027+7A>T rs72466580
NM_004006.2(DMD):c.8308G>A (p.Asp2770Asn) rs138399787
NM_004006.2(DMD):c.8757C>T (p.Asn2919=) rs753234741
NM_004006.2(DMD):c.8974G>A (p.Val2992Met) rs201691420
NM_004006.2(DMD):c.94-9T>A rs3764764
NM_004006.2(DMD):c.9486G>A (p.Glu3162=) rs370724251
NM_004006.2(DMD):c.9682T>C (p.Phe3228Leu) rs141392048

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