"Ambry Genetics"[submitter] AND "ETS1"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2485991	NM_001143820.2(ETS1):c.1423G>A (p.Ala475Thr)	ETS1 (A215T +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2273561	NM_001143820.2(ETS1):c.1013C>T (p.Ala338Val)	ETS1 (A294V +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2397936	NM_001143820.2(ETS1):c.859C>T (p.Arg287Cys)	ETS1 (R243C +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2305026	NM_001143820.2(ETS1):c.808A>G (p.Ile270Val)	ETS1 (I226V +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2523581	NM_001143820.2(ETS1):c.665C>T (p.Pro222Leu)	ETS1 (P178L +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2607365	NM_001143820.2(ETS1):c.650C>T (p.Ser217Leu)	ETS1 (S173L +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance

ClinVar