Related gene-specific medical variations for Gene (Select 200316) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2527491	NM_145298.6(APOBEC3F):c.697T>C (p.Trp233Arg)	APOBEC3F, LOC126863152 (W233R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2527489	NM_145298.6(APOBEC3F):c.695C>T (p.Ser232Phe)	APOBEC3F, LOC126863152 (S232F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2525139	NM_145298.6(APOBEC3F):c.688C>G (p.Pro230Ala)	APOBEC3F, LOC126863152 (P230A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2335140	NM_145298.6(APOBEC3F):c.695C>G (p.Ser232Cys)	APOBEC3F, LOC126863152 (S232C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2274716	NM_145298.6(APOBEC3F):c.622C>T (p.Arg208Cys)	APOBEC3F, LOC126863152 (R208C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 781619	NM_145298.6(APOBEC3F):c.573G>A (p.Pro191=)	APOBEC3F, LOC126863152	Single nucleotide variant (synonymous variant)	not provided	GBenign

ClinVar