ClinVar Miner

List of variants in gene DMD reported as likely benign for Duchenne muscular dystrophy

Included ClinVar conditions (3):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 129
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HGVS dbSNP
NM_000109.3(DMD):c.7547G>A (p.Arg2516His) rs151244052
NM_000109.3(DMD):c.9658T>C (p.Phe3220Leu) rs141392048
NM_004006.2(DMD):c.10087-8C>A rs1261494456
NM_004006.2(DMD):c.1008G>A (p.Glu336=) rs1280118173
NM_004006.2(DMD):c.10122G>A (p.Lys3374=) rs1556037420
NM_004006.2(DMD):c.10224T>A (p.Thr3408=) rs774389538
NM_004006.2(DMD):c.10308C>T (p.Arg3436=) rs780389106
NM_004006.2(DMD):c.10362T>C (p.Tyr3454=) rs1556028072
NM_004006.2(DMD):c.10593C>T (p.His3531=) rs753460206
NM_004006.2(DMD):c.10620G>A (p.Pro3540=) rs72466538
NM_004006.2(DMD):c.10725G>A (p.Arg3575=) rs147346696
NM_004006.2(DMD):c.1084T>C (p.Leu362=) rs1556876311
NM_004006.2(DMD):c.10921+7G>T rs1060504677
NM_004006.2(DMD):c.1122G>C (p.Val374=) rs769001938
NM_004006.2(DMD):c.1382A>G (p.Asn461Ser) rs775115784
NM_004006.2(DMD):c.1383T>C (p.Asn461=) rs373729675
NM_004006.2(DMD):c.1473A>G (p.Gln491=) rs144303432
NM_004006.2(DMD):c.1503A>G (p.Glu501=) rs770464589
NM_004006.2(DMD):c.1513G>C (p.Val505Leu) rs140340626
NM_004006.2(DMD):c.1542G>C (p.Val514=) rs1556834846
NM_004006.2(DMD):c.1603-4C>A rs377223643
NM_004006.2(DMD):c.162C>T (p.Leu54=) rs904011265
NM_004006.2(DMD):c.1704+3G>A rs773123973
NM_004006.2(DMD):c.1704+8_1704+9delAT rs1556810175
NM_004006.2(DMD):c.1705-4G>A rs889499438
NM_004006.2(DMD):c.1707C>T (p.Cys569=) rs142029039
NM_004006.2(DMD):c.1812+4T>C rs777165271
NM_004006.2(DMD):c.1812C>T (p.Ala604=) rs140919039
NM_004006.2(DMD):c.1920G>A (p.Thr640=) rs766895256
NM_004006.2(DMD):c.1926A>G (p.Ala642=) rs1060504678
NM_004006.2(DMD):c.2076A>G (p.Glu692=) rs764950114
NM_004006.2(DMD):c.2166A>G (p.Lys722=) rs147580966
NM_004006.2(DMD):c.2352T>C (p.Ala784=) rs142006072
NM_004006.2(DMD):c.2400C>T (p.Ser800=) rs142115986
NM_004006.2(DMD):c.2422C>T (p.Leu808=) rs1289380956
NM_004006.2(DMD):c.2508T>C (p.Tyr836=) rs886044674
NM_004006.2(DMD):c.2523A>G (p.Gln841=) rs748655300
NM_004006.2(DMD):c.2575A>T (p.Thr859Ser) rs187926894
NM_004006.2(DMD):c.2612A>C (p.Lys871Thr) rs398123899
NM_004006.2(DMD):c.2682C>T (p.Ser894=) rs398123904
NM_004006.2(DMD):c.2745A>G (p.Thr915=) rs149922633
NM_004006.2(DMD):c.2804T>G (p.Ile935Ser) rs190247714
NM_004006.2(DMD):c.2858C>T (p.Thr953Ile) rs142133195
NM_004006.2(DMD):c.2910C>T (p.Thr970=) rs765442122
NM_004006.2(DMD):c.297C>T (p.Ile99=) rs1004456825
NM_004006.2(DMD):c.2988A>G (p.Leu996=) rs148835707
NM_004006.2(DMD):c.3096C>G (p.Leu1032=) rs770148717
NM_004006.2(DMD):c.3162+4A>G rs189048508
NM_004006.2(DMD):c.3177C>T (p.Thr1059=) rs755632126
NM_004006.2(DMD):c.3269A>T (p.Gln1090Leu) rs747239076
NM_004006.2(DMD):c.3375G>A (p.Ser1125=) rs191164314
NM_004006.2(DMD):c.3432+8C>A rs781003275
NM_004006.2(DMD):c.3445A>G (p.Lys1149Glu) rs144667422
NM_004006.2(DMD):c.3663A>G (p.Val1221=) rs750549006
NM_004006.2(DMD):c.3666T>C (p.Asn1222=) rs373281760
NM_004006.2(DMD):c.3924A>T (p.Ser1308=) rs1557357591
NM_004006.2(DMD):c.3988C>T (p.Leu1330=) rs1557357523
NM_004006.2(DMD):c.4093C>T (p.Leu1365Phe) rs148781346
NM_004006.2(DMD):c.4230C>G (p.Ala1410=) rs1375731794
NM_004006.2(DMD):c.4314A>G (p.Gln1438=) rs985982212
NM_004006.2(DMD):c.4497G>A (p.Gln1499=) rs1417062461
NM_004006.2(DMD):c.4698G>A (p.Leu1566=) rs1060504680
NM_004006.2(DMD):c.4744G>A (p.Val1582Ile) rs398123965
NM_004006.2(DMD):c.4747T>C (p.Leu1583=) rs1060504673
NM_004006.2(DMD):c.4845+7C>T rs764100658
NM_004006.2(DMD):c.4881C>T (p.His1627=) rs886043184
NM_004006.2(DMD):c.5040C>T (p.His1680=) rs72468632
NM_004006.2(DMD):c.5104T>C (p.Leu1702=) rs750664323
NM_004006.2(DMD):c.525T>C (p.Ser175=) rs113776167
NM_004006.2(DMD):c.530+7A>T rs72470523
NM_004006.2(DMD):c.5370A>C (p.Ile1790=) rs748336386
NM_004006.2(DMD):c.5418T>C (p.Asn1806=) rs149543306
NM_004006.2(DMD):c.5448+7T>C rs1557294172
NM_004006.2(DMD):c.5449-12_5449-10delGTT rs745728411
NM_004006.2(DMD):c.5449-7dup rs1557292841
NM_004006.2(DMD):c.5459A>G (p.Asn1820Ser) rs1800271
NM_004006.2(DMD):c.5476G>C (p.Glu1826Gln) rs140913030
NM_004006.2(DMD):c.5577T>C (p.Asn1859=) rs372707022
NM_004006.2(DMD):c.5583C>T (p.Leu1861=) rs775837149
NM_004006.2(DMD):c.5586+9G>A rs200025478
NM_004006.2(DMD):c.5688T>C (p.Ile1896=) rs1557291068
NM_004006.2(DMD):c.5739+8T>C rs1321625981
NM_004006.2(DMD):c.5933G>A (p.Arg1978His) rs148135406
NM_004006.2(DMD):c.5933G>T (p.Arg1978Leu) rs148135406
NM_004006.2(DMD):c.603C>T (p.Asn201=) rs750180929
NM_004006.2(DMD):c.6151C>T (p.Arg2051Trp) rs140791274
NM_004006.2(DMD):c.618A>G (p.Gln206=) rs727503865
NM_004006.2(DMD):c.624C>A (p.Gly208=) rs768761464
NM_004006.2(DMD):c.6320G>A (p.Arg2107Gln) rs142807436
NM_004006.2(DMD):c.6438+10T>C rs754382994
NM_004006.2(DMD):c.651T>C (p.Asp217=) rs1556930849
NM_004006.2(DMD):c.6614+7C>A rs180719577
NM_004006.2(DMD):c.6942A>G (p.Gly2314=) rs1556962536
NM_004006.2(DMD):c.7032A>G (p.Leu2344=) rs1556962392
NM_004006.2(DMD):c.7051T>C (p.Leu2351=) rs367747168
NM_004006.2(DMD):c.7183G>A (p.Ala2395Thr) rs72466590
NM_004006.2(DMD):c.7200+9G>A rs748786108
NM_004006.2(DMD):c.7281A>T (p.Leu2427=) rs886038872
NM_004006.2(DMD):c.7323T>C (p.Thr2441=) rs201919981
NM_004006.2(DMD):c.7578G>A (p.Gln2526=) rs142236825
NM_004006.2(DMD):c.7725G>A (p.Leu2575=) rs754604466
NM_004006.2(DMD):c.7781A>G (p.Gln2594Arg) rs777178221
NM_004006.2(DMD):c.7944C>T (p.Leu2648=) rs1060504675
NM_004006.2(DMD):c.831+10G>A rs756370588
NM_004006.2(DMD):c.832-3C>T rs777492476
NM_004006.2(DMD):c.8322G>A (p.Leu2774=) rs72466575
NM_004006.2(DMD):c.8355G>A (p.Lys2785=) rs772646759
NM_004006.2(DMD):c.8418G>A (p.Gln2806=) rs953271494
NM_004006.2(DMD):c.84A>G (p.Gln28=) rs1060504676
NM_004006.2(DMD):c.8532G>A (p.Gln2844=) rs887532907
NM_004006.2(DMD):c.861G>A (p.Glu287=) rs1284806719
NM_004006.2(DMD):c.8643A>G (p.Leu2881=) rs747605156
NM_004006.2(DMD):c.8712A>G (p.Leu2904=) rs764631900
NM_004006.2(DMD):c.8718G>A (p.Lys2906=) rs377178242
NM_004006.2(DMD):c.8767G>T (p.Ala2923Ser) rs116283249
NM_004006.2(DMD):c.8847G>A (p.Lys2949=) rs185664502
NM_004006.2(DMD):c.888C>T (p.Phe296=) rs977310228
NM_004006.2(DMD):c.8974G>A (p.Val2992Met) rs201691420
NM_004006.2(DMD):c.9033G>A (p.Pro3011=) rs774722438
NM_004006.2(DMD):c.9210G>T (p.Val3070=) rs147336953
NM_004006.2(DMD):c.9325G>T (p.Ala3109Ser) rs201718067
NM_004006.2(DMD):c.9564-5A>G rs201390145
NM_004006.2(DMD):c.960+9A>G rs886038537
NM_004006.2(DMD):c.9649+8G>A rs373703618
NM_004006.2(DMD):c.9651C>T (p.Tyr3217=) rs1313897024
NM_004006.2(DMD):c.9672T>C (p.Ser3224=) rs1060504679
NM_004006.2(DMD):c.9808-10G>A rs1060504674
NM_004006.2(DMD):c.9828C>T (p.Ile3276=) rs757899883
NM_004006.2(DMD):c.999A>G (p.Ser333=) rs748489730

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