FABP5[gene] and "single gene"[properties] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2595828	NM_001444.3(FABP5):c.86G>A (p.Gly29Glu)	FABP5 (G29E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3091551	NM_001444.3(FABP5):c.98G>A (p.Arg33Gln)	FABP5 (R33Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3091548	NM_001444.3(FABP5):c.130A>G (p.Ile44Val)	FABP5 (I44V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 97083	NM_001444.3(FABP5):c.279A>G (p.Ala93=)	FABP5	Single nucleotide variant (synonymous variant)	not provided	Gnot provided
Select item 718925	NM_001444.3(FABP5):c.289C>T (p.His97Tyr)	FABP5 (H97Y)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 97084	NM_001444.3(FABP5):c.331T>C (p.Leu111=)	FABP5	Single nucleotide variant (synonymous variant)	not provided	Gnot provided
Select item 97085	NM_001444.3(FABP5):c.371A>G (p.Asn124Ser)	FABP5 (N124S)	Single nucleotide variant (missense variant)	not provided	Gnot provided
Select item 3091550	NM_001444.3(FABP5):c.392A>G (p.Tyr131Cys)	FABP5 (Y131C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

ClinVar