ClinVar (all) for Orgtrack (Select 508417) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1335900	NM_000061.3(BTK):c.829G>T (p.Glu277Ter)	BTK (E277* +1 more)	Single nucleotide variant (nonsense)	X-linked agammaglobulinemia	GPathogenic
Select item 1334133	NM_000061.3(BTK):c.895-2del	BTK	Deletion (splice acceptor variant)	X-linked agammaglobulinemia	GPathogenic