FBP2[gene] and "single gene"[properties] - ClinVar - NCBI

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Items: 14

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2335438	NM_003837.4(FBP2):c.397A>G (p.Ile133Val)	FBP2 (I133V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1809604	NM_003837.4(FBP2):c.343G>A (p.Val115Met)	FBP2 (V115M)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2616522	NM_003837.4(FBP2):c.341A>G (p.Tyr114Cys)	FBP2 (Y114C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3093418	NM_003837.4(FBP2):c.310A>G (p.Ile104Val)	FBP2 (I104V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2673178	NM_003837.4(FBP2):c.257T>C (p.Val86Ala)	FBP2 (V86A)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 3278006	NM_003837.4(FBP2):c.211G>C (p.Val71Leu)	FBP2 (V71L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3278011	NM_003837.4(FBP2):c.88G>A (p.Glu30Lys)	FBP2 (E30K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3252056	NM_003837.4(FBP2):c.68G>A (p.Arg23His)	FBP2 (R23H)	Single nucleotide variant (missense variant)	Neurodevelopmental disorder	GUncertain significance
Select item 2256066	NM_003837.4(FBP2):c.47G>A (p.Arg16His)	FBP2 (R16H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2387282	NM_003837.4(FBP2):c.46C>T (p.Arg16Cys)	FBP2 (R16C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2618352	NM_003837.4(FBP2):c.41T>C (p.Leu14Pro)	FBP2 (L14P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2529005	NM_003837.4(FBP2):c.29A>G (p.Asp10Gly)	FBP2 (D10G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2549448	NM_003837.4(FBP2):c.19T>G (p.Phe7Val)	FBP2 (F7V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2343953	NM_003837.4(FBP2):c.5C>T (p.Thr2Met)	FBP2 (T2M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance