Related gene-specific medical variations for Gene (Select 7392) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3331265	NM_003367.4(USF2):c.349G>C (p.Val117Leu)	LOC130064218, USF2 (V117L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3187021	NM_003367.4(USF2):c.87G>T (p.Glu29Asp)	LOC130064217, USF2 (E29D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3187020	NM_003367.4(USF2):c.64C>A (p.His22Asn)	LOC130064217, USF2 (H22N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3187016	NM_003367.4(USF2):c.271G>C (p.Gly91Arg)	LOC130064218, USF2 (G91R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2604201	NM_003367.4(USF2):c.271G>A (p.Gly91Ser)	LOC130064218, USF2 (G91S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2380317	NM_003367.4(USF2):c.374G>A (p.Arg125His)	LOC130064218, USF2 (R125H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2340966	NM_003367.4(USF2):c.403C>T (p.Pro135Ser)	LOC130064218, USF2 (P135S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 161613	NM_003367.4(USF2):c.497G>A (p.Arg166Gln)	USF2 (R166Q +1 more)	Single nucleotide variant (missense variant +1 more)	Malignant tumor of prostate	GUncertain significance

ClinVar