"Clinical Genetics, Academic Medical Center"[submitter] AND "DMD"[gene - ClinVar - NCBI

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Items: 17

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 94854	NM_004006.3(DMD):c.9649+15T>C	DMD	Single nucleotide variant (intron variant)	Duchenne muscular dystrophy +3 more	GBenign
Select item 166667	NM_004006.3(DMD):c.8810G>A (p.Arg2937Gln)	DMD (R2937Q +5 more)	Single nucleotide variant (missense variant +1 more)	Dilated cardiomyopathy 3B +3 more	GBenign
Select item 11269	NM_004006.3(DMD):c.8762A>G (p.His2921Arg)	DMD (H2921R +7 more)	Single nucleotide variant (missense variant)	not specified +5 more	GBenign/Likely benign
Select item 94783	NM_004006.3(DMD):c.8027+11C>T	DMD	Single nucleotide variant (intron variant)	Duchenne muscular dystrophy +3 more	GBenign
Select item 94741	NM_004006.3(DMD):c.6463C>T (p.Arg2155Trp)	DMD (R2155W +5 more)	Single nucleotide variant (missense variant +1 more)	Duchenne muscular dystrophy +5 more	GBenign/Likely benign
Select item 94657	NM_004006.3(DMD):c.5234G>A (p.Arg1745His)	DMD (R1745H +5 more)	Single nucleotide variant (missense variant)	Duchenne muscular dystrophy +4 more	GBenign
Select item 94604	NM_004006.3(DMD):c.3734C>T (p.Thr1245Ile)	DMD (T1245I +3 more)	Single nucleotide variant (missense variant)	Dilated cardiomyopathy 3B +4 more	GBenign
Select item 1174745	NM_004006.3(DMD):c.3603+3_3603+4dup	DMD	Duplication (intron variant)	Duchenne muscular dystrophy	GLikely benign
Select item 195965	NM_004006.3(DMD):c.3603+3dup	DMD	Duplication (intron variant)	not specified +2 more	GBenign/Likely benign
Select item 94599	NM_004006.3(DMD):c.3603+15del	DMD	Deletion (intron variant)	not specified +1 more	GBenign
Select item 166842	NM_004006.3(DMD):c.2645A>G (p.Asp882Gly)	DMD (D882G +1 more)	Single nucleotide variant (missense variant +1 more)	not specified +3 more	GBenign
Select item 94510	NM_004006.3(DMD):c.2391T>G (p.Asn797Lys)	DMD (N797K +3 more)	Single nucleotide variant (missense variant)	not provided +5 more	GBenign/Likely benign
Select item 94495	NM_004006.3(DMD):c.2168+13T>C	DMD	Single nucleotide variant (intron variant)	Dilated cardiomyopathy 3B +3 more	GBenign
Select item 94476	NM_004006.3(DMD):c.1635A>G (p.Arg545=)	DMD	Single nucleotide variant (synonymous variant)	not provided +5 more	GBenign
Select item 94799	NM_004006.3(DMD):c.832-17C>A	DMD	Single nucleotide variant (intron variant)	Duchenne muscular dystrophy +4 more	GBenign/Likely benign
Select item 94800	NM_004006.3(DMD):c.832-18C>G	DMD	Single nucleotide variant (intron variant)	not specified +1 more	GBenign
Select item 94844	NM_004006.3(DMD):c.94-9dup	DMD	Duplication (intron variant)	Duchenne muscular dystrophy +4 more	GBenign/Likely benign