"Ambry Genetics"[submitter] AND "ETS2"[gene] - ClinVar

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Items: 31

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2213533	NM_005239.6(ETS2):c.73C>T (p.Arg25Cys)	ETS2 (R165C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2466717	NM_005239.6(ETS2):c.74G>A (p.Arg25His)	ETS2 (R165H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2248234	NM_005239.6(ETS2):c.196T>C (p.Cys66Arg)	ETS2, LOC126653370 (C206R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2601519	NM_005239.6(ETS2):c.237G>A (p.Met79Ile)	ETS2, LOC126653370 (M219I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3090719	NM_005239.6(ETS2):c.283C>T (p.Arg95Trp)	ETS2, LOC126653370 (R235W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2353264	NM_005239.6(ETS2):c.284G>A (p.Arg95Gln)	ETS2, LOC126653370 (R95Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3090720	NM_005239.6(ETS2):c.335G>A (p.Cys112Tyr)	ETS2, LOC126653370 (C252Y +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3276597	NM_005239.6(ETS2):c.397G>A (p.Gly133Ser)	ETS2, LOC126653370 (G133S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2468772	NM_005239.6(ETS2):c.566A>G (p.His189Arg)	ETS2 (H189R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2219789	NM_005239.6(ETS2):c.614A>T (p.Tyr205Phe)	ETS2 (Y345F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2220263	NM_005239.6(ETS2):c.621G>A (p.Met207Ile)	ETS2 (M347I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2623070	NM_005239.6(ETS2):c.655G>A (p.Asp219Asn)	ETS2 (D219N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3090721	NM_005239.6(ETS2):c.668C>T (p.Pro223Leu)	ETS2 (P223L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2395645	NM_005239.6(ETS2):c.685G>A (p.Val229Ile)	ETS2 (V229I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3276601	NM_005239.6(ETS2):c.691A>C (p.Ser231Arg)	ETS2 (S371R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3276599	NM_005239.6(ETS2):c.697G>C (p.Glu233Gln)	ETS2 (E233Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3090722	NM_005239.6(ETS2):c.700C>G (p.Gln234Glu)	ETS2 (Q234E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2240240	NM_005239.6(ETS2):c.718C>T (p.Pro240Ser)	ETS2 (P240S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3276600	NM_005239.6(ETS2):c.728G>A (p.Arg243Gln)	ETS2 (R383Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2408031	NM_005239.6(ETS2):c.739G>A (p.Val247Ile)	ETS2 (V247I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3090723	NM_005239.6(ETS2):c.847G>A (p.Ala283Thr)	ETS2 (A283T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2280120	NM_005239.6(ETS2):c.848C>T (p.Ala283Val)	ETS2 (A283V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2265649	NM_005239.6(ETS2):c.859G>C (p.Glu287Gln)	ETS2 (E427Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2293042	NM_005239.6(ETS2):c.979C>T (p.Pro327Ser)	ETS2 (P327S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3276596	NM_005239.6(ETS2):c.985A>G (p.Met329Val)	ETS2 (M329V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3090724	NM_005239.6(ETS2):c.986T>A (p.Met329Lys)	ETS2 (M469K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2466668	NM_005239.6(ETS2):c.1057G>A (p.Val353Met)	ETS2 (V353M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2369888	NM_005239.6(ETS2):c.1066G>A (p.Gly356Ser)	ETS2 (G496S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3090717	NM_005239.6(ETS2):c.1072A>G (p.Thr358Ala)	ETS2 (T358A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3090718	NM_005239.6(ETS2):c.1127A>G (p.Lys376Arg)	ETS2 (K376R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2478530	NM_005239.6(ETS2):c.1301C>T (p.Ser434Leu)	ETS2 (S574L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 31