DMD[gene] and "single gene"[properties] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 915100	NM_004006.3(DMD):c.*2585T>G	DMD	Single nucleotide variant (3 prime UTR variant)	Dilated cardiomyopathy 3B	GUncertain significance
Select item 915101	NM_004006.3(DMD):c.*2563G>A	DMD	Single nucleotide variant (3 prime UTR variant)	Dilated cardiomyopathy 3B	GLikely benign
Select item 915102	NM_004006.3(DMD):c.*2328G>A	DMD	Single nucleotide variant (3 prime UTR variant)	Dilated cardiomyopathy 3B	GUncertain significance
Select item 368199	NM_004006.3(DMD):c.*2314T>C	DMD	Single nucleotide variant (3 prime UTR variant)	Dilated cardiomyopathy 3B	GUncertain significance
Select item 915103	NM_004006.3(DMD):c.*2268C>T	DMD	Single nucleotide variant (3 prime UTR variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 368200	NM_004006.3(DMD):c.2234_2238dup	DMD	Duplication (3 prime UTR variant)	Dilated cardiomyopathy 3B	GUncertain significance
Select item 368201	NM_004006.3(DMD):c.*2226AAGT[4]	DMD	Microsatellite (3 prime UTR variant)	Dilated cardiomyopathy 3B	GUncertain significance
Select item 915104	NM_004006.3(DMD):c.*2103T>A	DMD	Single nucleotide variant (3 prime UTR variant)	Dilated cardiomyopathy 3B	GUncertain significance
Select item 368203	NM_004006.3(DMD):c.*2039C>A	DMD	Single nucleotide variant (3 prime UTR variant)	Dilated cardiomyopathy 3B	GLikely benign
Select item 368202	NM_004006.3(DMD):c.2037_2038dup	DMD	Duplication (3 prime UTR variant)	Dilated cardiomyopathy 3B	GLikely benign
Select item 368204	NM_004006.3(DMD):c.2031_2034dup	DMD	Duplication (3 prime UTR variant)	Dilated cardiomyopathy 3B	GUncertain significance
Select item 912397	NM_004006.3(DMD):c.*1917G>A	DMD	Single nucleotide variant (3 prime UTR variant)	Dilated cardiomyopathy 3B	GUncertain significance
Select item 912398	NM_004006.3(DMD):c.*1799G>T	DMD	Single nucleotide variant (3 prime UTR variant)	Dilated cardiomyopathy 3B	GBenign
Select item 368205	NM_004006.3(DMD):c.*1783A>G	DMD	Single nucleotide variant (3 prime UTR variant)	not provided +1 more	GBenign
Select item 368206	NM_004006.3(DMD):c.*1754TTCA[1]	DMD	Microsatellite (3 prime UTR variant)	Dilated cardiomyopathy 3B	GUncertain significance
Select item 368207	NM_004006.3(DMD):c.*1731A>C	DMD	Single nucleotide variant (3 prime UTR variant)	Dilated cardiomyopathy 3B	GBenign
Select item 912399	NM_004006.3(DMD):c.*1705A>G	DMD	Single nucleotide variant (3 prime UTR variant)	Dilated cardiomyopathy 3B	GLikely benign
Select item 368208	NM_004006.3(DMD):c.*1638A>G	DMD	Single nucleotide variant (3 prime UTR variant)	Dilated cardiomyopathy 3B +1 more	GBenign
Select item 368209	NM_004006.3(DMD):c.1588_1591dup	DMD	Duplication (3 prime UTR variant)	Dilated cardiomyopathy 3B	GUncertain significance
Select item 368210	NM_004006.3(DMD):c.*1554TAAG[4]	DMD	Microsatellite (3 prime UTR variant)	Dilated cardiomyopathy 3B	GLikely benign
Select item 368211	NM_004006.3(DMD):c.*1455C>A	DMD	Single nucleotide variant (3 prime UTR variant)	Dilated cardiomyopathy 3B	GLikely benign
Select item 368212	NM_004006.3(DMD):c.1448_1449insAAGA	DMD	Insertion (3 prime UTR variant)	Dilated cardiomyopathy 3B	GUncertain significance
Select item 368213	NM_004006.3(DMD):c.*1447A>G	DMD	Single nucleotide variant (3 prime UTR variant)	not provided +1 more	GBenign
Select item 368214	NM_004006.3(DMD):c.*1421TAAA[3]	DMD	Microsatellite (3 prime UTR variant)	Dilated cardiomyopathy 3B	GUncertain significance
Select item 368215	NM_004006.3(DMD):c.*1349T>G	DMD	Single nucleotide variant (3 prime UTR variant)	Dilated cardiomyopathy 3B	GUncertain significance
Select item 368216	NM_004006.3(DMD):c.*1339G>C	DMD	Single nucleotide variant (3 prime UTR variant)	Dilated cardiomyopathy 3B	GUncertain significance
Select item 368217	NM_004006.3(DMD):c.*1285C>A	DMD	Single nucleotide variant (3 prime UTR variant)	Dilated cardiomyopathy 3B	GBenign
Select item 368218	NM_004006.3(DMD):c.1161_1164dup	DMD	Duplication (3 prime UTR variant)	Dilated cardiomyopathy 3B	GUncertain significance
Select item 368219	NM_004006.3(DMD):c.*1033TGAT[6]	DMD	Microsatellite (3 prime UTR variant)	not provided +1 more	GUncertain significance
Select item 368220	NM_004006.3(DMD):c.*1033TGAT[4]	DMD	Microsatellite (3 prime UTR variant)	not provided +1 more	GUncertain significance
Select item 368221	NM_004006.3(DMD):c.*1049T>C	DMD	Single nucleotide variant (3 prime UTR variant)	Dilated cardiomyopathy 3B	GUncertain significance
Select item 2440859	NM_004006.3(DMD):c.*1023GTTG[4]	DMD	Microsatellite (3 prime UTR variant)	not provided	GUncertain significance
Select item 913517	NM_004006.3(DMD):c.*1035A>G	DMD	Single nucleotide variant (3 prime UTR variant)	Dilated cardiomyopathy 3B	GLikely benign
Select item 913518	NM_004006.3(DMD):c.*1031G>A	DMD	Single nucleotide variant (3 prime UTR variant)	Dilated cardiomyopathy 3B	GUncertain significance
Select item 913519	NM_004006.3(DMD):c.*1023G>A	DMD	Single nucleotide variant (3 prime UTR variant)	Dilated cardiomyopathy 3B	GUncertain significance
Select item 368222	NM_004006.3(DMD):c.*1005T>G	DMD	Single nucleotide variant (3 prime UTR variant)	Dilated cardiomyopathy 3B	GUncertain significance
Select item 368223	NM_004006.3(DMD):c.*942AAGTA[4]	DMD	Microsatellite (3 prime UTR variant)	Dilated cardiomyopathy 3B	GUncertain significance
Select item 913898	NM_004006.3(DMD):c.*855G>A	DMD	Single nucleotide variant (3 prime UTR variant)	Dilated cardiomyopathy 3B	GLikely benign
Select item 913899	NM_004006.3(DMD):c.*848C>T	DMD	Single nucleotide variant (3 prime UTR variant)	Dilated cardiomyopathy 3B	GUncertain significance
Select item 368224	NM_004006.3(DMD):c.*803GTCA[3]	DMD	Microsatellite (3 prime UTR variant)	Dilated cardiomyopathy 3B	GUncertain significance
Select item 913900	NM_004006.3(DMD):c.*809C>T	DMD	Single nucleotide variant (3 prime UTR variant)	Dilated cardiomyopathy 3B	GBenign
Select item 368225	NM_004006.3(DMD):c.*704C>T	DMD	Single nucleotide variant (3 prime UTR variant)	Dilated cardiomyopathy 3B	GUncertain significance
Select item 913901	NM_004006.3(DMD):c.*571A>G	DMD	Single nucleotide variant (3 prime UTR variant)	Dilated cardiomyopathy 3B	GLikely benign
Select item 913902	NM_004006.3(DMD):c.*505A>G	DMD	Single nucleotide variant (3 prime UTR variant)	Dilated cardiomyopathy 3B	GUncertain significance
Select item 368226	NM_004006.3(DMD):c.*479CA[9]	DMD	Microsatellite (3 prime UTR variant)	Dilated cardiomyopathy 3B	GUncertain significance
Select item 368227	NM_004006.3(DMD):c.*479CA[6]	DMD	Microsatellite (3 prime UTR variant)	Dilated cardiomyopathy 3B +1 more	GConflicting classifications of pathogenicity
Select item 913903	NM_004006.3(DMD):c.*489C>T	DMD	Single nucleotide variant (3 prime UTR variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 368230	NM_004006.3(DMD):c.*477T>C	DMD	Single nucleotide variant (3 prime UTR variant)	Dilated cardiomyopathy 3B	GLikely benign
Select item 368229	NM_004006.3(DMD):c.*461CA[10]	DMD	Microsatellite (3 prime UTR variant)	Dilated cardiomyopathy 3B	GUncertain significance
Select item 368228	NM_004006.3(DMD):c.*461CA[9]	DMD	Microsatellite (3 prime UTR variant)	Dilated cardiomyopathy 3B	GUncertain significance
Select item 368231	NM_004006.3(DMD):c.*237T>C	DMD	Single nucleotide variant (3 prime UTR variant)	Dilated cardiomyopathy 3B	GUncertain significance
Select item 915145	NM_004006.3(DMD):c.*218G>A	DMD	Single nucleotide variant (3 prime UTR variant)	Dilated cardiomyopathy 3B	GUncertain significance
Select item 368232	NM_004006.3(DMD):c.*192G>A	DMD	Single nucleotide variant (3 prime UTR variant)	Dilated cardiomyopathy 3B	GUncertain significance
Select item 583951	NC_000023.10:g.(?_31139930)_(31140067_?)dup	DMD	Duplication	Duchenne muscular dystrophy	GUncertain significance
Select item 1190376	NM_004006.3(DMD):c.57_60dup	DMD (M1126fs +4 more)	Duplication (frameshift variant +1 more)	not provided	GUncertain significance
Select item 379121	NM_004006.3(DMD):c.*59C>A	DMD	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GLikely benign
Select item 978757	NM_004006.3(DMD):c.*39A>T	DMD (M1119L +4 more)	Single nucleotide variant (3 prime UTR variant +1 more)	Primary dilated cardiomyopathy	GLikely benign
Select item 226569	NM_004006.3(DMD):c.*38G>A	DMD	Single nucleotide variant (3 prime UTR variant +1 more)	not specified +2 more	GBenign
Select item 201754	NM_004006.3(DMD):c.23_35del	DMD (D1223fs +4 more)	Deletion (3 prime UTR variant +1 more)	Primary familial dilated cardiomyopathy +3 more	GConflicting classifications of pathogenicity
Select item 504876	NM_004006.3(DMD):c.*24G>A	DMD (D1224N +4 more)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 377776	NM_004006.3(DMD):c.*15A>G	DMD (M613V +4 more)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GLikely benign
Select item 583255	NM_004006.3(DMD):c.11054T>C (p.Met3685Thr)	DMD (M3685T +10 more)	Single nucleotide variant (missense variant +1 more)	Duchenne muscular dystrophy +1 more	GUncertain significance
Select item 2769815	NM_004006.3(DMD):c.11052A>T (p.Thr3684=)	DMD (N593Y +4 more)	Single nucleotide variant (synonymous variant +1 more)	Duchenne muscular dystrophy	GLikely benign
Select item 2703886	NM_004006.3(DMD):c.11052A>C (p.Thr3684=)	DMD (N1201H +4 more)	Single nucleotide variant (synonymous variant +1 more)	Duchenne muscular dystrophy	GLikely benign
Select item 1160748	NM_004006.3(DMD):c.11052A>G (p.Thr3684=)	DMD (N1104D +4 more)	Single nucleotide variant (synonymous variant +1 more)	Duchenne muscular dystrophy	GLikely benign
Select item 2043166	NM_004006.3(DMD):c.11047-3dup	DMD	Duplication (intron variant)	Duchenne muscular dystrophy	GLikely benign
Select item 2909057	NM_004006.3(DMD):c.11047-3C>T	DMD	Single nucleotide variant (intron variant)	Duchenne muscular dystrophy	GUncertain significance
Select item 2154935	NM_004006.3(DMD):c.11047-5T>C	DMD	Single nucleotide variant (intron variant)	Duchenne muscular dystrophy	GLikely benign
Select item 2146848	NM_004006.3(DMD):c.11047-9_11047-6dup	DMD	Duplication (intron variant)	Duchenne muscular dystrophy	GLikely benign
Select item 1514671	NM_004006.3(DMD):c.11047-34_11047-7dup	DMD	Duplication (intron variant)	Duchenne muscular dystrophy	GLikely benign
Select item 2091568	NM_004006.3(DMD):c.11047-32_11047-8dup	DMD	Duplication (intron variant)	Duchenne muscular dystrophy	GLikely benign
Select item 2193036	NM_004006.3(DMD):c.11047-10T>C	DMD	Single nucleotide variant (intron variant)	Duchenne muscular dystrophy	GLikely benign
Select item 1926634	NM_004006.3(DMD):c.11047-13_11047-10del	DMD	Deletion (intron variant)	Duchenne muscular dystrophy	GLikely benign
Select item 1571382	NM_004006.3(DMD):c.11047-15_11047-10del	DMD	Deletion (intron variant)	Duchenne muscular dystrophy	GLikely benign
Select item 700670	NM_004006.3(DMD):c.11047-11_11047-10del	DMD	Deletion (intron variant)	Duchenne muscular dystrophy	GLikely benign
Select item 2992975	NM_004006.3(DMD):c.11047-15CT[4]	DMD	Microsatellite (intron variant)	Duchenne muscular dystrophy	GLikely benign
Select item 2838559	NM_004006.3(DMD):c.11047-12T>C	DMD	Single nucleotide variant (intron variant)	Duchenne muscular dystrophy	GLikely benign
Select item 2183930	NM_004006.3(DMD):c.11047-21TTCT[3]	DMD	Microsatellite (intron variant)	Duchenne muscular dystrophy	GLikely benign
Select item 2796898	NM_004006.3(DMD):c.11047-14T>G	DMD	Single nucleotide variant (intron variant)	Duchenne muscular dystrophy	GLikely benign
Select item 1603458	NM_004006.3(DMD):c.11047-17_11047-14del	DMD	Microsatellite (intron variant)	Duchenne muscular dystrophy	GBenign
Select item 421505	NM_004006.3(DMD):c.11047-20dup	DMD	Duplication (intron variant)	not specified	GLikely benign
Select item 672567	NM_004006.3(DMD):c.11047-150dup	DMD	Duplication (intron variant)	not provided	GBenign
Select item 681746	NM_004006.3(DMD):c.11047-249A>T	DMD	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 672565	NM_004006.3(DMD):c.11046+119A>G	DMD	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1269108	NM_004006.3(DMD):c.11046+40T>C	DMD	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1624882	NM_004006.3(DMD):c.11046+19C>A	DMD	Single nucleotide variant (intron variant)	Duchenne muscular dystrophy	GLikely benign
Select item 1615009	NM_004006.3(DMD):c.11046+18T>G	DMD	Single nucleotide variant (intron variant)	Duchenne muscular dystrophy	GLikely benign
Select item 2894946	NM_004006.3(DMD):c.11046+11T>A	DMD	Single nucleotide variant (intron variant)	Duchenne muscular dystrophy	GLikely benign
Select item 379297	NM_004006.3(DMD):c.11046+11T>C	DMD	Single nucleotide variant (intron variant)	Duchenne muscular dystrophy +1 more	GBenign/Likely benign
Select item 2027898	NM_004006.3(DMD):c.11046+10A>G	DMD	Single nucleotide variant (intron variant)	Duchenne muscular dystrophy	GLikely benign
Select item 1133846	NM_004006.3(DMD):c.11046+9G>A	DMD	Single nucleotide variant (intron variant)	Duchenne muscular dystrophy	GLikely benign
Select item 2674873	NM_004006.3(DMD):c.11046+2T>C	DMD	Single nucleotide variant (splice donor variant +1 more)	Becker muscular dystrophy	GLikely pathogenic
Select item 3251612	NM_004006.3(DMD):c.11046+1G>A	DMD	Single nucleotide variant (splice donor variant +1 more)	not specified	GUncertain significance
Select item 2440854	NM_004006.3(DMD):c.11045A>T (p.Glu3682Val)	DMD (E1112V +10 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2154885	NM_004006.3(DMD):c.11044G>C (p.Glu3682Gln)	DMD (E601Q +10 more)	Single nucleotide variant (missense variant +1 more)	Duchenne muscular dystrophy	GUncertain significance
Select item 641807	NM_004006.3(DMD):c.11041A>T (p.Arg3681Ter)	DMD (R613* +10 more)	Single nucleotide variant (nonsense +1 more)	not specified +3 more	GUncertain significance
Select item 1620472	NM_004006.3(DMD):c.11031A>G (p.Gly3677=)	DMD	Single nucleotide variant (synonymous variant +1 more)	Dilated cardiomyopathy 3B +2 more	GLikely benign
Select item 2440828	NM_004006.3(DMD):c.11030G>A (p.Gly3677Glu)	DMD (G1107E +10 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2061097	NM_004006.3(DMD):c.11027C>T (p.Pro3676Leu)	DMD (P2335L +10 more)	Single nucleotide variant (missense variant +1 more)	Duchenne muscular dystrophy	GUncertain significance
Select item 455858	NM_004006.3(DMD):c.11023A>G (p.Thr3675Ala)	DMD (T3675A +10 more)	Single nucleotide variant (missense variant +1 more)	Cardiovascular phenotype +3 more	GUncertain significance

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