Related gene-specific medical variations for Gene (Select 126805658) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3274283	NM_004091.4(E2F2):c.616A>G (p.Lys206Glu)	E2F2, LOC126805658 (K206E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3086738	NM_004091.4(E2F2):c.736A>G (p.Arg246Gly)	E2F2, LOC126805658 (R246G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3086737	NM_004091.4(E2F2):c.460G>A (p.Asp154Asn)	E2F2, LOC101928163 +1 more (D154N)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2561310	NM_004091.4(E2F2):c.668C>T (p.Ala223Val)	E2F2, LOC126805658 (A223V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2526057	NM_004091.4(E2F2):c.439G>A (p.Glu147Lys)	E2F2, LOC101928163 +1 more (E147K)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 713748	NM_004091.4(E2F2):c.605C>T (p.Thr202Ile)	E2F2, LOC126805658 (T202I)	Single nucleotide variant (missense variant)	not provided	GLikely benign

ClinVar