Related gene-specific medical variations for Gene (Select 25790) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3143502	NM_012337.3(CFAP45):c.250C>T (p.Arg84Trp)	CFAP45, LOC126805888 (R84W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2512588	NM_012337.3(CFAP45):c.170T>G (p.Leu57Arg)	CFAP45, LOC126805888 (L57R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2284854	NM_012337.3(CFAP45):c.205G>A (p.Ala69Thr)	CFAP45, LOC126805888 (A69T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2284853	NM_012337.3(CFAP45):c.181C>A (p.His61Asn)	CFAP45, LOC126805888 (H61N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2265474	NM_012337.3(CFAP45):c.221G>A (p.Arg74His)	CFAP45, LOC126805888 (R74H)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2210955	NM_012337.3(CFAP45):c.169C>T (p.Leu57Phe)	CFAP45, LOC126805888 (L57F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

ClinVar