ClinVar Miner

List of variants in gene DMD reported as likely benign by PreventionGenetics, part of Exact Sciences

Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 90
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HGVS dbSNP gnomAD frequency
NM_004006.3(DMD):c.6463C>T (p.Arg2155Trp) rs1800273 0.02767
NM_004006.3(DMD):c.31+36946C>T rs186833917 0.00211
NM_004006.3(DMD):c.8571T>C (p.Thr2857=) rs72466570 0.00153
NM_004006.3(DMD):c.5265C>T (p.Pro1755=) rs145515413 0.00124
NM_004006.3(DMD):c.1513G>C (p.Val505Leu) rs140340626 0.00113
NM_004006.3(DMD):c.2261G>T (p.Gly754Val) rs151242451 0.00098
NM_004006.3(DMD):c.1731A>T (p.Glu577Asp) rs150199251 0.00073
NM_004006.3(DMD):c.4093C>T (p.Leu1365Phe) rs148781346 0.00071
NM_004006.3(DMD):c.5476G>C (p.Glu1826Gln) rs140913030 0.00071
NM_004006.3(DMD):c.4233+2C>T rs147474070 0.00066
NM_004006.3(DMD):c.2199C>T (p.Ser733=) rs149882431 0.00064
NM_004006.3(DMD):c.5203C>T (p.Arg1735Cys) rs147904018 0.00054
NM_004006.3(DMD):c.4072-245C>T rs140237546 0.00046
NM_004006.3(DMD):c.5586+9G>A rs200025478 0.00044
NM_004006.3(DMD):c.6732G>C (p.Gln2244His) rs142531761 0.00043
NM_004006.3(DMD):c.6828C>T (p.Pro2276=) rs72466595 0.00039
NM_004006.3(DMD):c.1934A>G (p.Asp645Gly) rs147822019 0.00036
NM_004006.3(DMD):c.6320G>A (p.Arg2107Gln) rs142807436 0.00036
NM_004006.3(DMD):c.10836C>T (p.Ser3612=) rs148590546 0.00033
NM_004006.3(DMD):c.8767G>T (p.Ala2923Ser) rs116283249 0.00032
NM_004006.3(DMD):c.8076A>G (p.Gln2692=) rs144518527 0.00025
NM_004006.3(DMD):c.9165G>A (p.Thr3055=) rs137905486 0.00024
NM_004006.3(DMD):c.1337A>G (p.His446Arg) rs72468699 0.00023
NM_004006.3(DMD):c.8138A>G (p.Asn2713Ser) rs758633794 0.00022
NM_004006.3(DMD):c.6571C>T (p.Arg2191Trp) rs149322279 0.00020
NM_004006.3(DMD):c.7521C>T (p.Asn2507=) rs112516305 0.00020
NM_004006.3(DMD):c.94-3C>T rs373907950 0.00018
NM_004006.3(DMD):c.2858C>T (p.Thr953Ile) rs142133195 0.00017
NM_004006.3(DMD):c.4876G>A (p.Val1626Met) rs776998846 0.00014
NM_004006.3(DMD):c.357+5G>A rs778431187 0.00013
NM_004006.3(DMD):c.7244G>A (p.Arg2415His) rs373749120 0.00013
NM_004006.3(DMD):c.8706G>A (p.Arg2902=) rs899851642 0.00013
NM_004006.3(DMD):c.9563+4C>T rs753666498 0.00013
NM_004006.3(DMD):c.9479G>A (p.Arg3160His) rs771392678 0.00012
NM_004006.3(DMD):c.1318G>A (p.Glu440Lys) rs189143447 0.00010
NM_004006.3(DMD):c.4940C>T (p.Thr1647Met) rs148868095 0.00009
NM_004006.3(DMD):c.2988A>G (p.Leu996=) rs148835707 0.00007
NM_004006.3(DMD):c.9093C>T (p.Val3031=) rs72466563 0.00007
NM_004006.3(DMD):c.1824G>A (p.Ala608=) rs151013182 0.00006
NM_004006.3(DMD):c.2667A>T (p.Arg889=) rs759593799 0.00005
NM_004006.3(DMD):c.3432+8C>A rs781003275 0.00005
NM_004006.3(DMD):c.4456C>T (p.Pro1486Ser) rs762125605 0.00005
NM_004006.3(DMD):c.6132T>C (p.Ser2044=) rs761338933 0.00005
NM_004006.3(DMD):c.8886C>T (p.Pro2962=) rs371648038 0.00005
NM_004006.3(DMD):c.1503A>G (p.Glu501=) rs770464589 0.00004
NM_004006.3(DMD):c.1603-6C>T rs774626474 0.00004
NM_004006.3(DMD):c.2117C>A (p.Pro706Gln) rs781015830 0.00004
NM_004006.3(DMD):c.5104T>C (p.Leu1702=) rs750664323 0.00004
NM_004006.3(DMD):c.8926G>A (p.Glu2976Lys) rs142128738 0.00004
NM_004006.3(DMD):c.10203A>G (p.Leu3401=) rs371928525 0.00003
NM_004006.3(DMD):c.3814T>C (p.Leu1272=) rs746405191 0.00003
NM_004006.3(DMD):c.5869C>T (p.Arg1957Trp) rs755477994 0.00003
NM_004006.3(DMD):c.6614+7C>T rs180719577 0.00003
NM_004006.3(DMD):c.8958G>A (p.Ala2986=) rs755815057 0.00003
NM_004006.3(DMD):c.960+9A>G rs886038537 0.00003
NM_004006.3(DMD):c.*59C>A rs1057520501 0.00002
NM_004006.3(DMD):c.1299C>T (p.Cys433=) rs372135475 0.00002
NM_004006.3(DMD):c.2842A>G (p.Met948Val) rs186628781 0.00002
NM_004006.3(DMD):c.5235C>T (p.Arg1745=) rs766312119 0.00002
NM_004006.3(DMD):c.5827A>G (p.Met1943Val) rs181849614 0.00002
NM_004006.3(DMD):c.8226A>G (p.Gln2742=) rs746514008 0.00002
NM_004006.3(DMD):c.1464C>T (p.Arg488=) rs771891715 0.00001
NM_004006.3(DMD):c.3030G>A (p.Ala1010=) rs72468666 0.00001
NM_004006.3(DMD):c.3635C>T (p.Ala1212Val) rs142171890 0.00001
NM_004006.3(DMD):c.597A>C (p.Ala199=) rs918198867 0.00001
NM_004006.3(DMD):c.6896A>C (p.Asn2299Thr) rs747055774 0.00001
NM_004006.3(DMD):c.7016A>G (p.His2339Arg) rs398124041 0.00001
NM_004006.3(DMD):c.8847G>A (p.Lys2949=) rs185664502 0.00001
NM_004006.3(DMD):c.*23_*35del rs752332058
NM_004006.3(DMD):c.1482+314G>T
NM_004006.3(DMD):c.1584T>C (p.Ala528=)
NM_004006.3(DMD):c.1869C>G (p.Leu623=) rs1800267
NM_004006.3(DMD):c.1993-10C>T rs1226290209
NM_004006.3(DMD):c.2173G>T (p.Asp725Tyr) rs398123879
NM_004006.3(DMD):c.2273A>C (p.Asp758Ala) rs750526692
NM_004006.3(DMD):c.3433-20GTTT[2] rs771258264
NM_004006.3(DMD):c.3787-846G>A
NM_004006.3(DMD):c.4115C>T (p.Ala1372Val) rs759108067
NM_004006.3(DMD):c.5740-14G>A
NM_004006.3(DMD):c.650-39504C>T
NM_004006.3(DMD):c.7653G>A (p.Thr2551=) rs368803197
NM_004006.3(DMD):c.7661-1656G>A
NM_004006.3(DMD):c.8217+18042T>C
NM_004006.3(DMD):c.8217+32101G>A
NM_004006.3(DMD):c.9030A>T (p.Ser3010=)
NM_004006.3(DMD):c.9048T>C (p.Thr3016=)
NM_004006.3(DMD):c.932A>G (p.Asp311Gly) rs760932600
NM_004006.3(DMD):c.94-9del rs3834997
NM_004006.3(DMD):c.9564-437T>A
NM_004006.3(DMD):c.961-5922A>G

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