"Institute for Clinical Genetics, University Hospital TU Dresden, Univ - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1319136	NM_004006.3(DMD):c.7942C>T (p.Leu2648Phe)	DMD (L1304F +6 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 409909	NM_004006.3(DMD):c.7892G>A (p.Arg2631His)	DMD (R2631H +6 more)	Single nucleotide variant (missense variant)	Duchenne muscular dystrophy +2 more	GConflicting classifications of pathogenicity
Select item 1319138	NM_004006.3(DMD):c.6225G>A (p.Gln2075=)	DMD	Single nucleotide variant (synonymous variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 1319137	NM_004006.3(DMD):c.2984G>T (p.Gly995Val)	DMD (G872V +3 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1319139	NM_004006.3(DMD):c.2479G>A (p.Glu827Lys)	DMD (E704K +3 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1015076	NM_004006.3(DMD):c.881C>T (p.Pro294Leu)	DMD (P171L +3 more)	Single nucleotide variant (missense variant)	Duchenne muscular dystrophy +2 more	GUncertain significance
Select item 2575931	NM_004006.3(DMD):c.567del (p.Gln189fs)	DMD (Q181fs +3 more)	Deletion (frameshift variant)	not provided	GPathogenic

ClinVar