"Ambry Genetics"[submitter] AND "CD28"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3140493	NM_006139.4(CD28):c.44A>G (p.Gln15Arg)	CD28 (Q15R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2208444	NM_006139.4(CD28):c.116G>C (p.Ser39Thr)	CD28 (S39T +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3140491	NM_006139.4(CD28):c.277G>A (p.Glu93Lys)	CD28 (E93K +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2392428	NM_006139.4(CD28):c.307T>G (p.Tyr103Asp)	CD28 (Y103D +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2530704	NM_006139.4(CD28):c.445C>T (p.Pro149Ser)	CD28 (P30S +3 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2556924	NM_006139.4(CD28):c.505C>A (p.Leu169Ile)	CD28 (L169I +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2454950	NM_006139.4(CD28):c.607C>T (p.Arg203Cys)	CD28 (R217C +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

ClinVar