ClinVar Miner

List of variants reported as benign for Becker muscular dystrophy; Duchenne muscular dystrophy; Cardiomyopathy; Dystrophin deficiency

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Total variants: 66
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HGVS dbSNP gnomAD frequency
NM_004006.3(DMD):c.8810G>A (p.Arg2937Gln) rs1800280 0.95243
NM_004006.3(DMD):c.9649+15T>C rs2293668 0.84201
NM_004006.3(DMD):c.1993-37T>G rs115571 0.71699
NM_004006.3(DMD):c.2645A>G (p.Asp882Gly) rs228406 0.69509
NM_004006.3(DMD):c.9361+138T>C rs10127360 0.51217
NM_004006.3(DMD):c.5234G>A (p.Arg1745His) rs1801187 0.36912
NM_004006.3(DMD):c.8027+11C>T rs2270672 0.33026
NM_004006.3(DMD):c.2168+13T>C rs228373 0.32216
NM_004006.3(DMD):c.9563+1150A>G rs10482232 0.29944
NM_004006.3(DMD):c.6439-143G>A rs3761605 0.29636
NM_004006.3(DMD):c.9225-675A>G rs12015000 0.25497
NM_004006.3(DMD):c.7096A>C (p.Lys2366Gln) rs1800275 0.21153
NM_004006.3(DMD):c.6913-114A>T rs45618538 0.18012
NM_004006.3(DMD):c.7728T>C (p.Asn2576=) rs1801188 0.15883
NM_004006.3(DMD):c.9225-138A>G rs17338423 0.13760
NM_004006.3(DMD):c.837G>A (p.Thr279=) rs1800265 0.12849
NM_004006.3(DMD):c.1635A>G (p.Arg545=) rs5927083 0.12751
NM_004006.3(DMD):c.6614+3294G>A rs5972467 0.12147
NM_004006.3(DMD):c.6290+27T>A rs3788896 0.12062
NM_004006.3(DMD):c.93+5601G>T rs34892244 0.10143
NM_004006.3(DMD):c.93+5593T>A rs34352997 0.10114
NM_004006.3(DMD):c.1704+51T>C rs5927082 0.09293
NM_004006.3(DMD):c.9225-603T>G rs111482252 0.07490
NM_004006.3(DMD):c.1483-72T>C rs17309542 0.07230
NM_004006.3(DMD):c.8669-75C>G rs17338583 0.06936
NM_004006.3(DMD):c.4234-13A>G rs41303181 0.05327
NM_004006.3(DMD):c.3432+2089A>T rs147073545 0.03762
NM_004006.3(DMD):c.8734A>G (p.Asn2912Asp) rs1800278 0.02976
NM_004006.3(DMD):c.8729A>T (p.Glu2910Val) rs41305353 0.02876
NM_004006.3(DMD):c.4162T>G (p.Phe1388Val) rs28715870 0.02748
NM_004006.3(DMD):c.31+292A>C rs114046794 0.02592
NM_004006.3(DMD):c.2623-11C>G rs1028360 0.02567
NM_004006.3(DMD):c.-8T>A rs113726961 0.02450
NM_004006.3(DMD):c.4878G>T (p.Val1626=) rs61733574 0.02120
NM_004006.3(DMD):c.5016T>A (p.Asn1672Lys) rs16990264 0.02084
NM_004006.3(DMD):c.832-17C>A rs72470514 0.01678
NM_004006.3(DMD):c.3705C>T (p.Ala1235=) rs143628111 0.01510
NM_004006.3(DMD):c.832-18C>G rs72470515 0.01505
NM_004006.3(DMD):c.7310-36C>T rs72466586 0.01045
NM_004006.3(DMD):c.3734C>T (p.Thr1245Ile) rs1800269 0.01009
NM_004006.3(DMD):c.8668+19A>G rs148241865 0.01001
NM_004006.3(DMD):c.-419A>G rs150939177 0.00821
NM_004006.3(DMD):c.1332-18C>T rs193153078 0.00806
NM_004006.3(DMD):c.1997C>T (p.Ser666Leu) rs34563188 0.00460
NM_004006.3(DMD):c.1718C>T (p.Ala573Val) rs5972599 0.00436
NM_004006.3(DMD):c.7542+13A>G rs72466585 0.00407
NM_004006.3(DMD):c.3406A>T (p.Thr1136Ser) rs3827462 0.00356
NM_004006.3(DMD):c.3276+17A>T rs184220727 0.00329
NM_004006.3(DMD):c.8218-798G>A rs149479376 0.00299
NM_004006.3(DMD):c.3970C>T (p.Arg1324Cys) rs143184877 0.00208
NM_004006.3(DMD):c.5586+18A>G rs189522063 0.00031
NM_004006.3(DMD):c.5163G>C (p.Lys1721Asn) rs72468630 0.00021
NM_004006.3(DMD):c.5485C>G (p.Gln1829Glu) rs754765424 0.00018
NM_004006.3(DMD):c.4275A>G (p.Glu1425=) rs72468647 0.00004
NM_004006.3(DMD):c.1869C>T (p.Leu623=) rs1800267
NM_004006.3(DMD):c.2569C>T (p.Pro857Ser) rs552275776
NM_004006.3(DMD):c.3603+15del rs5902031
NM_004006.3(DMD):c.7200+53C>G rs1379871
NM_004006.3(DMD):c.8217+18141AC[9] rs74965499
NM_004006.3(DMD):c.9225-607C>A rs35710613
NM_004006.3(DMD):c.94-9dup rs3834997
NM_004006.3(DMD):c.9563+1245T>G rs1921709
NM_004006.3(DMD):c.9563+1301T>C rs5927706
NM_004006.3(DMD):c.961-5853C>T rs5972633
NM_004006.3(DMD):c.961-5978_961-5977insAGG rs200672281
NM_004006.3(DMD):c.961-5981A>T rs112213679

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