"GeneDx"[submitter] AND "CD79B"[gene] - ClinVar - NCBI

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Items: 11

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1231409	NM_000626.4(CD79B):c.*154C>T	CD79B, GH-LCR	Single nucleotide variant (3 prime UTR variant)	not provided	GBenign
Select item 1272184	NM_000626.4(CD79B):c.*153C>G	CD79B, GH-LCR	Single nucleotide variant (3 prime UTR variant)	not provided	GBenign
Select item 1287682	NM_000626.4(CD79B):c.*89T>C	CD79B, GH-LCR	Single nucleotide variant (3 prime UTR variant)	not specified +1 more	GBenign
Select item 1279839	NM_000626.4(CD79B):c.549+133A>G	CD79B, GH-LCR	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 402520	NM_000626.4(CD79B):c.366T>C (p.Cys122=)	CD79B, GH-LCR	Single nucleotide variant (synonymous variant +1 more)	not specified +2 more	GBenign
Select item 1291751	NM_000626.4(CD79B):c.118+258G>A	CD79B, GH-LCR	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 513622	NM_000626.4(CD79B):c.90A>G (p.Arg30=)	CD79B, GH-LCR	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 1225594	NM_000626.4(CD79B):c.68-140G>A	CD79B, GH-LCR	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1231551	NM_000626.4(CD79B):c.68-220A>C	CD79B, GH-LCR	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1269874	NC_000017.11:g.63932631A>G	CD79B, GH-LCR	Single nucleotide variant	not provided	GBenign
Select item 253549	GRCh37/hg19 17q22-23.3(chr17:56321134-62080001)x3	TANC2, DDX42 +66 more	Copy number gain	See cases	GPathogenic