ClinVar (all) for Orgtrack (Select 506651) - ClinVar - NCBI

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Items: 5

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1342922	NM_004006.3(DMD):c.1402_1403del (p.Glu468fs)	DMD (E345fs +3 more)	Deletion (frameshift variant)	Duchenne muscular dystrophy	GLikely pathogenic
Select item 1342921	NM_004006.3(DMD):c.287del (p.Ser96fs)	DMD (S88fs +2 more)	Deletion (frameshift variant +1 more)	Duchenne muscular dystrophy	GLikely pathogenic
Select item 1342920	NM_004006.3(DMD):c.2416_2417del (p.Glu806fs)	DMD (E683fs +3 more)	Deletion (frameshift variant)	Duchenne muscular dystrophy	GLikely pathogenic
Select item 1342919	NM_004006.3(DMD):c.5114C>A (p.Ser1705Ter)	DMD (S1582* +5 more)	Single nucleotide variant (nonsense)	Duchenne muscular dystrophy	GLikely pathogenic
Select item 1342918	NM_004006.3(DMD):c.3210del (p.Phe1070_Leu1071insTer)	DMD	Deletion (frameshift variant)	Duchenne muscular dystrophy	GLikely pathogenic

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