DMD Arg1844* - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2996555	NM_004006.3(DMD):c.5901A>G (p.Arg1967=)	DMD	Single nucleotide variant (synonymous variant)	Duchenne muscular dystrophy	GLikely benign
Select item 1158720	NM_004006.3(DMD):c.5900G>A (p.Arg1967Gln)	DMD (R1844Q +5 more)	Single nucleotide variant (missense variant)	Duchenne muscular dystrophy	GLikely benign
Select item 11258	NM_004006.3(DMD):c.5899C>T (p.Arg1967Ter)	DMD (R1967* +5 more)	Single nucleotide variant (nonsense)	Cardiovascular phenotype +2 more	GPathogenic
Select item 409932	NM_004006.3(DMD):c.5531G>A (p.Arg1844Gln)	DMD (R1844Q +5 more)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +1 more	GConflicting classifications of pathogenicity
Select item 975989	NM_004006.3(DMD):c.5530del (p.Arg1844fs)	DMD (R1721fs +5 more)	Deletion (frameshift variant)	Duchenne muscular dystrophy	GLikely pathogenic
Select item 289167	NM_004006.3(DMD):c.5530C>A (p.Arg1844=)	DMD	Single nucleotide variant (synonymous variant)	not specified +3 more	GConflicting classifications of pathogenicity
Select item 94669	NM_004006.3(DMD):c.5530C>T (p.Arg1844Ter)	DMD (R1844* +5 more)	Single nucleotide variant (nonsense)	not provided +1 more	GPathogenic

ClinVar