DMD Trp2915* - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1071899	NM_004006.3(DMD):c.8745G>A (p.Trp2915Ter)	DMD (W1571* +7 more)	Single nucleotide variant (nonsense)	Duchenne muscular dystrophy	GPathogenic
Select item 946689	NM_004006.3(DMD):c.8745G>T (p.Trp2915Cys)	DMD (W2915C +7 more)	Single nucleotide variant (missense variant)	Duchenne muscular dystrophy +1 more	GUncertain significance
Select item 803815	NM_004006.3(DMD):c.8744G>A (p.Trp2915Ter)	DMD (W2792* +7 more)	Single nucleotide variant (nonsense)	Duchenne muscular dystrophy	GPathogenic

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ClinVar