CD274[gene] and "single gene"[properties] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1274128	NC_000009.12:g.5450497G>C	CD274	Single nucleotide variant	not provided	GBenign
Select item 792122	NM_014143.4(CD274):c.198A>G (p.Gln66=)	CD274	Single nucleotide variant (synonymous variant +2 more)	not provided	GBenign
Select item 738348	NM_014143.4(CD274):c.363C>A (p.Ala121=)	CD274	Single nucleotide variant (synonymous variant +2 more)	not provided	GBenign
Select item 2659049	NM_014143.4(CD274):c.437C>G (p.Pro146Arg)	CD274 (P146R +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 2208831	NM_014143.4(CD274):c.548A>C (p.Asn183Thr)	CD274 (N69T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3140479	NM_014143.4(CD274):c.649G>A (p.Glu217Lys)	CD274 (E103K +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2307554	NM_014143.4(CD274):c.829A>G (p.Thr277Ala)	CD274 (T163A +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 1251725	NM_014143.4(CD274):c.*93G>A	CD274	Single nucleotide variant (3 prime UTR variant +1 more)	not provided	GBenign
Select item 1251890	NM_014143.4(CD274):c.*2635A>G	CD274	Single nucleotide variant (3 prime UTR variant +1 more)	not provided	GBenign

ClinVar