"Ambry Genetics"[submitter] AND "CD58"[gene] - ClinVar - NCBI

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Items: 12

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2620637	NM_001779.3(CD58):c.745T>G (p.Ser249Ala)	CD58 (S249A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2474344	NM_001779.3(CD58):c.736A>G (p.Arg246Gly)	CD58 (R246G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2405583	NM_001779.3(CD58):c.680C>T (p.Thr227Ile)	CD58 (T227I)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2294879	NM_001779.3(CD58):c.642C>G (p.His214Gln)	CD58 (H214Q)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3140623	NM_001779.3(CD58):c.626G>A (p.Ser209Asn)	CD58 (S209N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2337377	NM_001779.3(CD58):c.616A>G (p.Ile206Val)	CD58 (I206V)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2615172	NM_001779.3(CD58):c.487A>G (p.Met163Val)	CD58 (M163V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3264855	NM_001779.3(CD58):c.404A>C (p.Asn135Thr)	CD58 (N135T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2299242	NM_001779.3(CD58):c.328A>G (p.Ile110Val)	CD58 (I110V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3140622	NM_001779.3(CD58):c.320C>T (p.Ser107Leu)	CD58 (S107L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2282325	NM_001779.3(CD58):c.101A>G (p.Tyr34Cys)	CD58 (Y34C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3264856	NM_001779.3(CD58):c.71G>T (p.Gly24Val)	CD58 (G24V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance