List of variants in gene DMD reported as benign by Ambry Genetics

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 95

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HGVS	dbSNP	gnomAD frequency
NM_004006.3(DMD):c.5234G>A (p.Arg1745His)	rs1801187	0.36912
NM_004006.3(DMD):c.7728T>C (p.Asn2576=)	rs1801188	0.15883
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.8734A>G (p.Asn2912Asp)	rs1800278	0.02976
NM_004006.3(DMD):c.8729A>T (p.Glu2910Val)	rs41305353	0.02876
NM_004006.3(DMD):c.6463C>T (p.Arg2155Trp)	rs1800273	0.02767
NM_004006.3(DMD):c.4162T>G (p.Phe1388Val)	rs28715870	0.02748
NM_004006.3(DMD):c.8762A>G (p.His2921Arg)	rs1800279	0.02191
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.5724T>C (p.Asp1908=)	rs143159113	0.01630
NM_004006.3(DMD):c.3705C>T (p.Ala1235=)	rs143628111	0.01510
NM_004006.3(DMD):c.3021G>A (p.Ser1007=)	rs1800268	0.01212
NM_004006.3(DMD):c.1554T>A (p.Asp518Glu)	rs61733587	0.01098
NM_004006.3(DMD):c.1225A>T (p.Thr409Ser)	rs34155804	0.01079
NM_004006.3(DMD):c.3734C>T (p.Thr1245Ile)	rs1800269	0.01009
NM_004006.3(DMD):c.6322C>T (p.Arg2108Cys)	rs16990169	0.00981
NM_004006.3(DMD):c.2391T>G (p.Asn797Lys)	rs72468681	0.00714
NM_004006.3(DMD):c.7476T>C (p.Val2492=)	rs142153424	0.00626
NM_004006.3(DMD):c.2143A>T (p.Thr715Ser)	rs16998350	0.00594
NM_004006.3(DMD):c.10789C>T (p.Leu3597=)	rs1800281	0.00486
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.3406A>T (p.Thr1136Ser)	rs3827462	0.00356
NM_004006.3(DMD):c.5182C>T (p.Arg1728Cys)	rs34102501	0.00327
NM_004006.3(DMD):c.4529A>G (p.Lys1510Arg)	rs72468638	0.00279
NM_004006.3(DMD):c.3970C>T (p.Arg1324Cys)	rs143184877	0.00208
NM_004006.3(DMD):c.9682T>C (p.Phe3228Leu)	rs141392048	0.00180
NM_004006.3(DMD):c.2971G>C (p.Glu991Gln)	rs72468667	0.00146
NM_004006.3(DMD):c.7472A>G (p.Gln2491Arg)	rs147694734	0.00143
NM_004006.3(DMD):c.1888A>G (p.Thr630Ala)	rs72468692	0.00124
NM_004006.3(DMD):c.5984A>T (p.Tyr1995Phe)	rs147927593	0.00113
NM_004006.3(DMD):c.7571G>A (p.Arg2524His)	rs151244052	0.00109
NM_004006.3(DMD):c.2261G>T (p.Gly754Val)	rs151242451	0.00098
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.3326A>T (p.Asn1109Ile)	rs200596739	0.00064
NM_004006.3(DMD):c.8308G>A (p.Asp2770Asn)	rs138399787	0.00063
NM_004006.3(DMD):c.1028G>A (p.Arg343His)	rs61733589	0.00062
NM_004006.3(DMD):c.5487A>G (p.Gln1829=)	rs150787752	0.00055
NM_004006.3(DMD):c.3020C>T (p.Ser1007Leu)	rs144732570	0.00054
NM_004006.3(DMD):c.2381-3T>C	rs147931243	0.00048
NM_004006.3(DMD):c.2490C>T (p.Asn830=)	rs72468679	0.00040
NM_004006.3(DMD):c.6828C>T (p.Pro2276=)	rs72466595	0.00039
NM_004006.3(DMD):c.5181A>T (p.Ile1727=)	rs200887855	0.00038
NM_004006.3(DMD):c.1934A>G (p.Asp645Gly)	rs147822019	0.00036
NM_004006.3(DMD):c.1252A>T (p.Thr418Ser)	rs201341211	0.00026
NM_004006.3(DMD):c.3433G>C (p.Val1145Leu)	rs767442827	0.00026
NM_004006.3(DMD):c.2386G>A (p.Val796Ile)	rs139726281	0.00023
NM_004006.3(DMD):c.8138A>G (p.Asn2713Ser)	rs758633794	0.00022
NM_004006.3(DMD):c.2827C>T (p.Arg943Cys)	rs199986217	0.00021
NM_004006.3(DMD):c.5163G>C (p.Lys1721Asn)	rs72468630	0.00021
NM_004006.3(DMD):c.1666G>A (p.Asp556Asn)	rs182708940	0.00020
NM_004006.3(DMD):c.6571C>T (p.Arg2191Trp)	rs149322279	0.00020
NM_004006.3(DMD):c.2096C>G (p.Ala699Gly)	rs202008454	0.00018
NM_004006.3(DMD):c.2291A>G (p.Asn764Ser)	rs199588981	0.00018
NM_004006.3(DMD):c.8974G>A (p.Val2992Met)	rs201691420	0.00016
NM_004006.3(DMD):c.5723A>T (p.Asp1908Val)	rs145266970	0.00014
NM_004006.3(DMD):c.7151C>A (p.Ser2384Tyr)	rs185706283	0.00014
NM_004006.3(DMD):c.7988C>G (p.Thr2663Arg)	rs144103124	0.00013
NM_004006.3(DMD):c.821A>G (p.Tyr274Cys)	rs745868830	0.00013
NM_004006.3(DMD):c.9033G>A (p.Pro3011=)	rs774722438	0.00012
NM_004006.3(DMD):c.7323T>C (p.Thr2441=)	rs201919981	0.00010
NM_004006.3(DMD):c.10224T>A (p.Thr3408=)	rs774389538	0.00005
NM_004006.3(DMD):c.10577G>A (p.Arg3526His)	rs139547504	0.00005
NM_004006.3(DMD):c.3959C>G (p.Pro1320Arg)	rs766977775	0.00005
NM_004006.3(DMD):c.3941G>A (p.Arg1314Gln)	rs752767880	0.00004
NM_004006.3(DMD):c.4275A>G (p.Glu1425=)	rs72468647	0.00004
NM_004006.3(DMD):c.1059G>A (p.Ser353=)	rs760621626	0.00003
NM_004006.3(DMD):c.3419A>G (p.His1140Arg)	rs201297190	0.00003
NM_004006.3(DMD):c.4373T>A (p.Phe1458Tyr)	rs777274879	0.00003
NM_004006.3(DMD):c.8226A>G (p.Gln2742=)	rs746514008	0.00002
NM_004006.3(DMD):c.6140A>G (p.Gln2047Arg)	rs773782786	0.00001
NM_004006.3(DMD):c.8945G>A (p.Arg2982Gln)	rs750579766	0.00001
NM_004006.2:c.2645A>G
NM_004006.2:c.7096A>C
NM_004006.2:c.8810G>A
NM_004006.3(DMD):c.1332-13088_1332-11865del
NM_004006.3(DMD):c.1869C>T (p.Leu623=)	rs1800267
NM_004006.3(DMD):c.2273A>C (p.Asp758Ala)	rs750526692
NM_004006.3(DMD):c.2569C>T (p.Pro857Ser)	rs552275776
NM_004006.3(DMD):c.3603+2162_3603+2379del
NM_004006.3(DMD):c.3603+2163_3603+2362del
NM_004006.3(DMD):c.3603+2163_3603+2363del
NM_004006.3(DMD):c.3603+2163_3603+2369del
NM_004006.3(DMD):c.3603+2168_3603+2362del
NM_004006.3(DMD):c.3603+2173_3603+2362del
NM_004006.3(DMD):c.3603+2178_3603+2362del
NM_004006.3(DMD):c.4115C>T (p.Ala1372Val)	rs759108067
NM_004006.3(DMD):c.7653G>A (p.Thr2551=)	rs368803197
NM_004006.3(DMD):c.8973C>T (p.Asn2991=)	rs772306909
NM_004006.3(DMD):c.932A>G (p.Asp311Gly)	rs760932600
NM_004006.3(DMD):c.9410A>G (p.Asn3137Ser)	rs779737146

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