Related gene-specific medical variations for Gene (Select 2114) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
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 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 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 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 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 786688	NM_005239.6(ETS2):c.190G>A (p.Ala64Thr)	ETS2, LOC126653370 (A204T +1 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 771783	NM_005239.6(ETS2):c.243A>G (p.Gln81=)	ETS2, LOC126653370	Single nucleotide variant (synonymous variant)	not provided	GBenign/Likely benign

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