EIF4E1B[gene] and "single gene"[properties] - ClinVar - NCBI

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Items: 19

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3275037	NM_001099408.2(EIF4E1B):c.16G>T (p.Val6Leu)	EIF4E1B (V6L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2377924	NM_001099408.2(EIF4E1B):c.55G>A (p.Glu19Lys)	EIF4E1B (E19K)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2608270	NM_001099408.2(EIF4E1B):c.152C>T (p.Thr51Met)	EIF4E1B (T51M)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2467822	NM_001099408.2(EIF4E1B):c.201G>C (p.Arg67Ser)	EIF4E1B (R67S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2209829	NM_001099408.2(EIF4E1B):c.201G>T (p.Arg67Ser)	EIF4E1B (R67S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2245721	NM_001099408.2(EIF4E1B):c.457C>T (p.Arg153Trp)	EIF4E1B (R153W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2250897	NM_001099408.2(EIF4E1B):c.473C>T (p.Thr158Met)	EIF4E1B (T158M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2350156	NM_001099408.2(EIF4E1B):c.482G>A (p.Cys161Tyr)	EIF4E1B (C161Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2218732	NM_001099408.2(EIF4E1B):c.490G>C (p.Gly164Arg)	EIF4E1B (G164R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2363268	NM_001099408.2(EIF4E1B):c.509A>C (p.His170Pro)	EIF4E1B (H170P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2316235	NM_001099408.2(EIF4E1B):c.514A>G (p.Arg172Gly)	EIF4E1B (R172G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2407157	NM_001099408.2(EIF4E1B):c.584C>T (p.Ala195Val)	EIF4E1B (A195V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2327010	NM_001099408.2(EIF4E1B):c.616C>G (p.Arg206Gly)	EIF4E1B (R206G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3275035	NM_001099408.2(EIF4E1B):c.617G>T (p.Arg206Leu)	EIF4E1B (R206L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2615989	NM_001099408.2(EIF4E1B):c.637G>A (p.Gly213Ser)	EIF4E1B (G213S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2288724	NM_001099408.2(EIF4E1B):c.646C>T (p.Pro216Ser)	EIF4E1B (P216S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3275036	NM_001099408.2(EIF4E1B):c.659T>C (p.Ile220Thr)	EIF4E1B (I220T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2297164	NM_001099408.2(EIF4E1B):c.677C>T (p.Ala226Val)	EIF4E1B (A226V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2618678	NM_001099408.2(EIF4E1B):c.719T>C (p.Phe240Ser)	EIF4E1B (F240S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance