Related gene-specific medical variations for Gene (Select 8789) - ClinVar - NCBI

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Items: 10

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2659318	NM_003837.4(FBP2):c.504C>T (p.Tyr168=)	FBP2, PCAT7	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2620356	NM_003837.4(FBP2):c.635T>C (p.Leu212Pro)	PCAT7, FBP2 (L212P)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2524357	NM_003837.4(FBP2):c.544G>A (p.Val182Met)	FBP2, PCAT7 (V182M)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2494351	NM_003837.4(FBP2):c.779G>C (p.Gly260Ala)	FBP2, PCAT7 (G260A)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2486325	NM_003837.4(FBP2):c.509G>T (p.Ser170Ile)	FBP2, PCAT7 (S170I)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2316951	NM_003837.4(FBP2):c.545T>A (p.Val182Glu)	FBP2, PCAT7 (V182E)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2247909	NM_003837.4(FBP2):c.916G>T (p.Val306Leu)	FBP2, PCAT7 (V306L)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 1301656	NM_003837.4(FBP2):c.632G>A (p.Ser211Asn)	FBP2, PCAT7 (S211N)	Single nucleotide variant (missense variant)	not specified	GBenign
Select item 786143	NM_003837.4(FBP2):c.1019A>G (p.Ter340Trp)	FBP2, PCAT7	Single nucleotide variant (stop lost)	not provided	GBenign
Select item 776436	NM_003837.4(FBP2):c.675T>C (p.Thr225=)	FBP2, PCAT7	Single nucleotide variant (synonymous variant)	not provided	GBenign