Related gene-specific medical variations for Gene (Select 8857) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3278312	NM_003890.3(FCGBP):c.15676C>T (p.Arg5226Trp)	FCGBP, LOC126862906 (R5226W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3093997	NM_003890.3(FCGBP):c.15713C>T (p.Ser5238Phe)	FCGBP, LOC126862906 (S5238F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3093996	NM_003890.3(FCGBP):c.15586G>A (p.Glu5196Lys)	FCGBP, LOC126862906 (E5196K)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2649839	NM_003890.3(FCGBP):c.15702C>T (p.Leu5234=)	FCGBP, LOC126862906	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2543625	NM_003890.3(FCGBP):c.15718G>A (p.Gly5240Ser)	FCGBP, LOC126862906 (G5240S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2247255	NM_003890.3(FCGBP):c.15874G>A (p.Gly5292Ser)	FCGBP, LOC126862906 (G5292S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2226217	NM_003890.3(FCGBP):c.15619A>G (p.Thr5207Ala)	FCGBP, LOC126862906 (T5207A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2216004	NM_003890.3(FCGBP):c.15631G>A (p.Ala5211Thr)	FCGBP, LOC126862906 (A5211T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

ClinVar