ClinVar (all) for Orgtrack (Select 505498) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 208203	NM_013263.5(BRD7):c.1834C>T (p.Arg612Ter)	BRD7, LOC126862343 (R613* +1 more)	Single nucleotide variant (nonsense)	Granular cell cancer	GLikely pathogenic
Select item 208201	NM_001495.5(GFRA2):c.725C>T (p.Ser242Phe)	GFRA2 (S242F +2 more)	Single nucleotide variant (missense variant)	Pazopanib response	Gdrug response