"Ambry Genetics"[submitter] AND "CD3G"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 572829	NM_000073.3(CD3G):c.187G>A (p.Gly63Ser)	LOC126861358, CD3G (G63S)	Single nucleotide variant (missense variant)	not specified +1 more	GConflicting classifications of pathogenicity
Select item 2612612	NM_000073.3(CD3G):c.199G>A (p.Glu67Lys)	CD3G, LOC126861358 (E67K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 640654	NM_000073.3(CD3G):c.273G>C (p.Gln91His)	CD3G, LOC126861358 (Q91H)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 2338859	NM_000073.3(CD3G):c.334G>A (p.Ala112Thr)	CD3G, LOC126861358 (A112T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3140585	NM_000073.3(CD3G):c.409G>T (p.Ala137Ser)	CD3G, LOC126861358 (A137S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2620636	NM_000073.3(CD3G):c.515G>T (p.Ser172Ile)	CD3G (S172I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

ClinVar