"ITMI"[submitter] AND "CD79A"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 133831	NM_001783.4(CD79A):c.28G>A (p.Ala10Thr)	CD79A (A10T)	Single nucleotide variant (missense variant)	not specified +1 more	GConflicting classifications of pathogenicity
Select item 133832	NM_001783.4(CD79A):c.258C>A (p.Asp86Glu)	CD79A (D86E)	Single nucleotide variant (missense variant)	Agammaglobulinemia 3, autosomal recessive	GUncertain significance
Select item 133833	NM_001783.4(CD79A):c.320G>A (p.Arg107Gln)	CD79A (R107Q)	Single nucleotide variant (missense variant +1 more)	Agammaglobulinemia 3, autosomal recessive	GUncertain significance
Select item 133834	NM_001783.4(CD79A):c.371G>A (p.Arg124His)	CD79A (R124H)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GUncertain significance
Select item 133835	NM_001783.4(CD79A):c.419C>A (p.Thr140Asn)	CD79A (T140N +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 133837	NM_001783.4(CD79A):c.593T>C (p.Met198Thr)	CD79A (M198T +1 more)	Single nucleotide variant (missense variant)	Agammaglobulinemia 3, autosomal recessive	GUncertain significance
Select item 133836	NM_001783.4(CD79A):c.643A>G (p.Ser215Gly)	CD79A (S215G +1 more)	Single nucleotide variant (missense variant)	Agammaglobulinemia 3, autosomal recessive	GUncertain significance

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