"DMD-related disorder"[Disease/phenotype] AND "PreventionGenetics, par - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 379121	NM_004006.3(DMD):c.*59C>A	DMD	Single nucleotide variant (3 prime UTR variant +1 more)	DMD-related disorder +1 more	GLikely benign
Select item 201754	NM_004006.3(DMD):c.23_35del	DMD (D1223fs +4 more)	Deletion (3 prime UTR variant +1 more)	not specified +3 more	GConflicting classifications of pathogenicity
Select item 2632653	NM_004006.3(DMD):c.10981G>A (p.Glu3661Lys)	DMD (E1091K +11 more)	Single nucleotide variant (missense variant)	DMD-related disorder	GUncertain significance
Select item 518897	NM_004006.3(DMD):c.10836C>T (p.Ser3612=)	DMD	Single nucleotide variant (synonymous variant)	Duchenne muscular dystrophy +4 more	GBenign/Likely benign
Select item 1685700	NM_004006.3(DMD):c.10223+4A>G	DMD	Single nucleotide variant (stop lost +1 more)	DMD-related disorder +1 more	GConflicting classifications of pathogenicity
Select item 1141993	NM_004006.3(DMD):c.10203A>G (p.Leu3401=)	DMD	Single nucleotide variant (synonymous variant)	Duchenne muscular dystrophy +2 more	GLikely benign
Select item 94856	NM_004006.3(DMD):c.9682T>C (p.Phe3228Leu)	DMD (F3228L +8 more)	Single nucleotide variant (missense variant)	Duchenne muscular dystrophy +6 more	GBenign/Likely benign
Select item 3051416	NM_004006.3(DMD):c.9564-437T>A	DMD	Single nucleotide variant (intron variant)	DMD-related disorder	GLikely benign
Select item 511224	NM_004006.3(DMD):c.9563+4C>T	DMD	Single nucleotide variant (intron variant)	DMD-related disorder +3 more	GLikely benign
Select item 284712	NM_004006.3(DMD):c.9479G>A (p.Arg3160His)	DMD (R3160H +8 more)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +5 more	GConflicting classifications of pathogenicity
Select item 810544	NM_004006.3(DMD):c.9225-5795G>A	DMD (G7S)	Single nucleotide variant (missense variant +1 more)	DMD-related disorder +1 more	GBenign/Likely benign
Select item 286909	NM_004006.3(DMD):c.9165G>A (p.Thr3055=)	DMD	Single nucleotide variant (synonymous variant)	not specified +4 more	GConflicting classifications of pathogenicity
Select item 286182	NM_004006.3(DMD):c.9093C>T (p.Val3031=)	DMD	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype +3 more	GConflicting classifications of pathogenicity
Select item 2038464	NM_004006.3(DMD):c.9048T>C (p.Thr3016=)	DMD	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype +2 more	GLikely benign
Select item 3057679	NM_004006.3(DMD):c.9030A>T (p.Ser3010=)	DMD	Single nucleotide variant (synonymous variant)	DMD-related disorder	GLikely benign
Select item 497555	NM_004006.3(DMD):c.8958G>A (p.Ala2986=)	DMD	Single nucleotide variant (synonymous variant)	DMD-related disorder +3 more	GConflicting classifications of pathogenicity
Select item 389901	NM_004006.3(DMD):c.8886C>T (p.Pro2962=)	DMD	Single nucleotide variant (synonymous variant)	not provided +4 more	GConflicting classifications of pathogenicity
Select item 94816	NM_004006.3(DMD):c.8767G>T (p.Ala2923Ser)	DMD (A1579S +6 more)	Single nucleotide variant (missense variant)	Duchenne muscular dystrophy +4 more	GConflicting classifications of pathogenicity
Select item 11269	NM_004006.3(DMD):c.8762A>G (p.His2921Arg)	DMD (H2921R +7 more)	Single nucleotide variant (missense variant)	DMD-related disorder +5 more	GBenign/Likely benign
Select item 499297	NM_004006.3(DMD):c.8706G>A (p.Arg2902=)	DMD	Single nucleotide variant (synonymous variant)	DMD-related disorder +3 more	GConflicting classifications of pathogenicity
Select item 94810	NM_004006.3(DMD):c.8608C>T (p.Arg2870Ter)	DMD (R2870* +7 more)	Single nucleotide variant (nonsense)	Duchenne muscular dystrophy +2 more	GPathogenic
Select item 94809	NM_004006.3(DMD):c.8571T>C (p.Thr2857=)	DMD	Single nucleotide variant (synonymous variant)	Duchenne muscular dystrophy +4 more	GBenign/Likely benign
Select item 3056573	NM_004006.3(DMD):c.8217+32101G>A	DMD	Single nucleotide variant (intron variant)	DMD-related disorder	GLikely benign
Select item 3058256	NM_004006.3(DMD):c.8217+18042T>C	DMD	Single nucleotide variant (intron variant)	DMD-related disorder	GLikely benign
Select item 447266	NM_004006.3(DMD):c.8138A>G (p.Asn2713Ser)	DMD (N2713S +6 more)	Single nucleotide variant (missense variant)	not specified +4 more	GConflicting classifications of pathogenicity
Select item 197981	NM_004006.3(DMD):c.8076A>G (p.Gln2692=)	DMD	Single nucleotide variant (synonymous variant)	DMD-related disorder +4 more	GConflicting classifications of pathogenicity
Select item 3044946	NM_004006.3(DMD):c.7661-1656G>A	DMD	Single nucleotide variant (intron variant)	DMD-related disorder	GLikely benign
Select item 94771	NM_004006.3(DMD):c.7653G>A (p.Thr2551=)	DMD	Single nucleotide variant (synonymous variant)	Duchenne muscular dystrophy +5 more	GConflicting classifications of pathogenicity
Select item 284947	NM_004006.3(DMD):c.7521C>T (p.Asn2507=)	DMD	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype +5 more	GConflicting classifications of pathogenicity
Select item 227309	NM_004006.3(DMD):c.7244G>A (p.Arg2415His)	DMD (R2415H +5 more)	Single nucleotide variant (missense variant +1 more)	Duchenne muscular dystrophy +3 more	GBenign/Likely benign
Select item 287917	NM_004006.3(DMD):c.6896A>C (p.Asn2299Thr)	DMD (N2299T +5 more)	Single nucleotide variant (missense variant +1 more)	Cardiovascular phenotype +3 more	GConflicting classifications of pathogenicity
Select item 94747	NM_004006.3(DMD):c.6828C>T (p.Pro2276=)	DMD	Single nucleotide variant (synonymous variant +1 more)	Duchenne muscular dystrophy +5 more	GConflicting classifications of pathogenicity
Select item 197545	NM_004006.3(DMD):c.6732G>C (p.Gln2244His)	DMD (Q2244H +5 more)	Single nucleotide variant (missense variant +1 more)	DMD-related disorder +3 more	GBenign/Likely benign
Select item 290925	NM_004006.3(DMD):c.6614+7C>T	DMD	Single nucleotide variant (intron variant)	not provided +3 more	GConflicting classifications of pathogenicity
Select item 197522	NM_004006.3(DMD):c.6571C>T (p.Arg2191Trp)	DMD (R2191W +5 more)	Single nucleotide variant (missense variant +1 more)	Primary familial dilated cardiomyopathy +5 more	GConflicting classifications of pathogenicity
Select item 94702	NM_004006.3(DMD):c.6320G>A (p.Arg2107Gln)	DMD (R1984Q +4 more)	Single nucleotide variant (missense variant)	not specified +6 more	GConflicting classifications of pathogenicity
Select item 290206	NM_004006.3(DMD):c.6140A>G (p.Gln2047Arg)	DMD (Q2047R +5 more)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +4 more	GBenign/Likely benign
Select item 201753	NM_004006.3(DMD):c.5869C>T (p.Arg1957Trp)	DMD (R1957W +5 more)	Single nucleotide variant (missense variant)	DMD-related disorder +4 more	GConflicting classifications of pathogenicity
Select item 94683	NM_004006.3(DMD):c.5827A>G (p.Met1943Val)	DMD (M599V +4 more)	Single nucleotide variant (missense variant)	Duchenne muscular dystrophy +4 more	GConflicting classifications of pathogenicity
Select item 2720162	NM_004006.3(DMD):c.5740-14G>A	DMD	Single nucleotide variant (intron variant)	DMD-related disorder +1 more	GLikely benign
Select item 94674	NM_004006.3(DMD):c.5586+9G>A	DMD	Single nucleotide variant (intron variant)	Duchenne muscular dystrophy +4 more	GConflicting classifications of pathogenicity
Select item 228592	NM_004006.3(DMD):c.5476G>C (p.Glu1826Gln)	DMD (E1826Q +5 more)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +4 more	GConflicting classifications of pathogenicity
Select item 264304	NM_004006.3(DMD):c.5390T>C (p.Leu1797Pro)	DMD (L1797P +5 more)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +2 more	GUncertain significance
Select item 226567	NM_004006.3(DMD):c.5265C>T (p.Pro1755=)	DMD	Single nucleotide variant (synonymous variant)	not provided +4 more	GBenign/Likely benign
Select item 1646127	NM_004006.3(DMD):c.5235C>T (p.Arg1745=)	DMD	Single nucleotide variant (synonymous variant)	DMD-related disorder +2 more	GBenign/Likely benign
Select item 201749	NM_004006.3(DMD):c.5203C>T (p.Arg1735Cys)	DMD (R1735C +5 more)	Single nucleotide variant (missense variant)	DMD-related disorder +6 more	GConflicting classifications of pathogenicity
Select item 94656	NM_004006.3(DMD):c.5182C>T (p.Arg1728Cys)	DMD (R1728C +5 more)	Single nucleotide variant (missense variant)	Duchenne muscular dystrophy +5 more	GConflicting classifications of pathogenicity
Select item 455905	NM_004006.3(DMD):c.5163G>C (p.Lys1721Asn)	DMD (K1721N +5 more)	Single nucleotide variant (missense variant)	Duchenne muscular dystrophy +5 more	GBenign/Likely benign
Select item 526123	NM_004006.3(DMD):c.5104T>C (p.Leu1702=)	DMD	Single nucleotide variant (synonymous variant)	DMD-related disorder +2 more	GLikely benign
Select item 744957	NM_004006.3(DMD):c.4940C>T (p.Thr1647Met)	DMD (T1639M +5 more)	Single nucleotide variant (missense variant)	DMD-related disorder +2 more	GBenign/Likely benign
Select item 2637398	NM_004006.3(DMD):c.4876G>T (p.Val1626Leu)	DMD (V1503L +5 more)	Single nucleotide variant (missense variant)	DMD-related disorder	GUncertain significance
Select item 391221	NM_004006.3(DMD):c.4876G>A (p.Val1626Met)	DMD (V1626M +5 more)	Single nucleotide variant (missense variant)	not specified +3 more	GBenign/Likely benign
Select item 1743438	NM_004006.3(DMD):c.4831G>A (p.Val1611Ile)	DMD (V1488I +5 more)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +1 more	GUncertain significance
Select item 1106910	NM_004006.3(DMD):c.4456C>T (p.Pro1486Ser)	DMD (P1363S +5 more)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +3 more	GLikely benign
Select item 1368512	NM_004006.3(DMD):c.4328A>G (p.Gln1443Arg)	DMD (Q1320R +5 more)	Single nucleotide variant (missense variant)	DMD-related disorder +1 more	GUncertain significance
Select item 94616	NM_004006.3(DMD):c.4233+2C>T	DMD	Single nucleotide variant (splice donor variant)	not specified +6 more	GConflicting classifications of pathogenicity
Select item 522691	NM_004006.3(DMD):c.4115C>T (p.Ala1372Val)	DMD (A1372V +5 more)	Single nucleotide variant (missense variant)	DMD-related disorder +2 more	GBenign/Likely benign
Select item 94611	NM_004006.3(DMD):c.4093C>T (p.Leu1365Phe)	DMD (L1365F +5 more)	Single nucleotide variant (missense variant)	Duchenne muscular dystrophy +4 more	GConflicting classifications of pathogenicity
Select item 94610	NM_004006.3(DMD):c.4072-245C>T	DMD	Single nucleotide variant (intron variant +1 more)	not specified +2 more	GConflicting classifications of pathogenicity
Select item 285354	NM_004006.3(DMD):c.3814T>C (p.Leu1272=)	DMD	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype +3 more	GConflicting classifications of pathogenicity
Select item 3055023	NM_004006.3(DMD):c.3787-846G>A	DMD	Single nucleotide variant (intron variant)	DMD-related disorder	GLikely benign
Select item 3061386	NM_004006.3(DMD):c.3651dup (p.Thr1218fs)	DMD (T1095fs +3 more)	Duplication (frameshift variant)	DMD-related disorder	GPathogenic
Select item 498335	NM_004006.3(DMD):c.3635C>T (p.Ala1212Val)	DMD (A1212V +3 more)	Single nucleotide variant (missense variant)	not specified +2 more	GBenign/Likely benign
Select item 421901	NM_004006.3(DMD):c.3433-20GTTT[2]	DMD	Microsatellite (intron variant)	Duchenne muscular dystrophy +2 more	GConflicting classifications of pathogenicity
Select item 455893	NM_004006.3(DMD):c.3432+2036A>G	DMD	Single nucleotide variant (intron variant)	not provided +3 more	GPathogenic/Likely pathogenic
Select item 94590	NM_004006.3(DMD):c.3432+2036A>C	DMD	Single nucleotide variant (intron variant)	Duchenne muscular dystrophy +3 more	GBenign/Likely benign
Select item 526106	NM_004006.3(DMD):c.3432+8C>A	DMD	Single nucleotide variant (intron variant)	DMD-related disorder +2 more	GLikely benign
Select item 195818	NM_004006.3(DMD):c.3269A>T (p.Gln1090Leu)	DMD (Q1090L +3 more)	Single nucleotide variant (missense variant)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 518156	NM_004006.3(DMD):c.3030G>A (p.Ala1010=)	DMD	Single nucleotide variant (synonymous variant)	Duchenne muscular dystrophy +4 more	GConflicting classifications of pathogenicity
Select item 285127	NM_004006.3(DMD):c.2988A>G (p.Leu996=)	DMD	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype +3 more	GConflicting classifications of pathogenicity
Select item 226048	NM_004006.3(DMD):c.2972A>G (p.Glu991Gly)	DMD (E868G +3 more)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +2 more	GUncertain significance
Select item 1797745	NM_004006.3(DMD):c.2925G>A (p.Met975Ile)	DMD (M967I +3 more)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +1 more	GUncertain significance
Select item 388184	NM_004006.3(DMD):c.2858C>T (p.Thr953Ile)	DMD (T953I +3 more)	Single nucleotide variant (missense variant)	not specified +3 more	GConflicting classifications of pathogenicity
Select item 94541	NM_004006.3(DMD):c.2842A>G (p.Met948Val)	DMD (M948V +3 more)	Single nucleotide variant (missense variant)	Duchenne muscular dystrophy +4 more	GBenign/Likely benign
Select item 2631852	NM_004006.3(DMD):c.2788A>G (p.Lys930Glu)	DMD (K807E +3 more)	Single nucleotide variant (missense variant)	DMD-related disorder	GUncertain significance
Select item 455883	NM_004006.3(DMD):c.2667A>T (p.Arg889=)	DMD	Single nucleotide variant (synonymous variant)	Duchenne muscular dystrophy +2 more	GBenign/Likely benign
Select item 227307	NM_004006.3(DMD):c.2569C>T (p.Pro857Ser)	DMD (P857S +3 more)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +3 more	GBenign/Likely benign
Select item 2631358	NM_004006.3(DMD):c.2293-2A>G	DMD	Single nucleotide variant (splice acceptor variant)	DMD-related disorder	GPathogenic
Select item 2631017	NM_004006.3(DMD):c.2282_2287del (p.Glu761_Lys762del)	DMD	Deletion (inframe_deletion +1 more)	DMD-related disorder	GUncertain significance
Select item 201758	NM_004006.3(DMD):c.2273A>C (p.Asp758Ala)	DMD (D758A +3 more)	Single nucleotide variant (missense variant)	DMD-related disorder +5 more	GConflicting classifications of pathogenicity
Select item 194844	NM_004006.3(DMD):c.2261G>T (p.Gly754Val)	DMD (G754V +3 more)	Single nucleotide variant (missense variant)	Duchenne muscular dystrophy +5 more	GBenign/Likely benign
Select item 94498	NM_004006.3(DMD):c.2173G>T (p.Asp725Tyr)	DMD (D602Y +2 more)	Single nucleotide variant (missense variant)	Duchenne muscular dystrophy +2 more	GBenign/Likely benign
Select item 191244	NM_004006.3(DMD):c.2117C>A (p.Pro706Gln)	DMD (P706Q +3 more)	Single nucleotide variant (missense variant)	Dilated cardiomyopathy 3B +5 more	GConflicting classifications of pathogenicity
Select item 2630199	NM_004006.3(DMD):c.2114C>A (p.Pro705Gln)	DMD (P582Q +3 more)	Single nucleotide variant (missense variant)	DMD-related disorder	GUncertain significance
Select item 1158103	NM_004006.3(DMD):c.1993-10C>T	DMD	Single nucleotide variant (intron variant)	DMD-related disorder +1 more	GLikely benign
Select item 281435	NM_004006.3(DMD):c.1934A>G (p.Asp645Gly)	DMD (D645G +3 more)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +4 more	GConflicting classifications of pathogenicity
Select item 388592	NM_004006.3(DMD):c.1869C>G (p.Leu623=)	DMD	Single nucleotide variant (synonymous variant)	not specified +4 more	GBenign/Likely benign
Select item 377775	NM_004006.3(DMD):c.1824G>A (p.Ala608=)	DMD	Single nucleotide variant (synonymous variant)	not provided +3 more	GBenign/Likely benign
Select item 94478	NM_004006.3(DMD):c.1731A>T (p.Glu577Asp)	DMD (E569D +2 more)	Single nucleotide variant (missense variant)	Duchenne muscular dystrophy +4 more	GConflicting classifications of pathogenicity
Select item 499671	NM_004006.3(DMD):c.1603-6C>T	DMD	Single nucleotide variant (intron variant)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 3033871	NM_004006.3(DMD):c.1584T>C (p.Ala528=)	DMD	Single nucleotide variant (synonymous variant)	DMD-related disorder	GLikely benign
Select item 94471	NM_004006.3(DMD):c.1513G>C (p.Val505Leu)	DMD (V501L +2 more)	Single nucleotide variant (missense variant)	Duchenne muscular dystrophy +6 more	GBenign/Likely benign
Select item 227306	NM_004006.3(DMD):c.1503A>G (p.Glu501=)	DMD	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype +4 more	GBenign/Likely benign
Select item 3049514	NM_004006.3(DMD):c.1482+314G>T	DMD	Single nucleotide variant (intron variant)	DMD-related disorder	GLikely benign
Select item 1114758	NM_004006.3(DMD):c.1464C>T (p.Arg488=)	DMD	Single nucleotide variant (synonymous variant)	Duchenne muscular dystrophy +1 more	GLikely benign
Select item 94461	NM_004006.3(DMD):c.1337A>G (p.His446Arg)	DMD (H438R +2 more)	Single nucleotide variant (missense variant)	Duchenne muscular dystrophy +4 more	GConflicting classifications of pathogenicity
Select item 1128448	NM_004006.3(DMD):c.1299C>T (p.Cys433=)	DMD	Single nucleotide variant (synonymous variant)	Duchenne muscular dystrophy +2 more	GLikely benign
Select item 2632936	NM_004006.3(DMD):c.1259T>A (p.Val420Glu)	DMD (V297E +3 more)	Single nucleotide variant (missense variant)	DMD-related disorder	GUncertain significance
Select item 3045670	NM_004006.3(DMD):c.961-5922A>G	DMD	Single nucleotide variant (intron variant)	DMD-related disorder	GLikely benign
Select item 201743	NM_004006.3(DMD):c.932A>G (p.Asp311Gly)	DMD (D311G +3 more)	Single nucleotide variant (missense variant)	DMD-related disorder +3 more	GConflicting classifications of pathogenicity

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