"Ambry Genetics"[submitter] AND "EIF4E"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2618462	NM_001968.5(EIF4E):c.581T>C (p.Val194Ala)	EIF4E (V225A +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2555665	NM_001968.5(EIF4E):c.502A>T (p.Thr168Ser)	EIF4E (T168S +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2519517	NM_001968.5(EIF4E):c.326G>T (p.Arg109Leu)	EIF4E (R109L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2325901	NM_001968.5(EIF4E):c.187A>G (p.Ile63Val)	EIF4E (I83V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3087993	NM_001968.5(EIF4E):c.98A>G (p.His33Arg)	EIF4E (H33R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2273284	NM_001968.5(EIF4E):c.85G>A (p.Ala29Thr)	EIF4E (A29T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2490772	NM_001968.5(EIF4E):c.13G>A (p.Glu5Lys)	EIF4E (E5K)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance

ClinVar