Related gene-specific medical variations for Gene (Select 80233) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3091527	NM_025161.6(FAAP100):c.278C>T (p.Pro93Leu)	FAAP100, LOC130061951 (P93L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3091516	NM_025161.6(FAAP100):c.147G>C (p.Gln49His)	FAAP100, LOC130061952 (Q49H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2511335	NM_025161.6(FAAP100):c.61C>G (p.Leu21Val)	FAAP100, LOC130061952 (L21V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2403205	NM_025161.6(FAAP100):c.52C>T (p.Leu18Phe)	FAAP100, LOC130061952 (L18F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2323870	NM_025161.6(FAAP100):c.245G>A (p.Arg82Gln)	FAAP100, LOC130061951 (R82Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2262433	NM_025161.6(FAAP100):c.154G>T (p.Gly52Trp)	FAAP100, LOC130061952 (G52W)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

ClinVar