Related gene-specific medical variations for Gene (Select 3627) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3270399	NM_001565.4(CXCL10):c.244A>G (p.Ile82Val)	ART3, CXCL10 (I82V)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3079166	NM_001565.4(CXCL10):c.83T>C (p.Val28Ala)	ART3, CXCL10 (V28A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2517570	NM_001565.4(CXCL10):c.202A>G (p.Lys68Glu)	ART3, CXCL10 (K68E)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2327969	NM_001565.4(CXCL10):c.158C>T (p.Ala53Val)	ART3, CXCL10 (A53V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2214856	NM_001565.4(CXCL10):c.89G>A (p.Cys30Tyr)	ART3, CXCL10 (C30Y)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 773454	NM_001565.4(CXCL10):c.85C>T (p.Arg29Cys)	ART3, CXCL10 (R29C)	Single nucleotide variant (missense variant +1 more)	not provided	GBenign
Select item 731714	NM_001565.4(CXCL10):c.243C>A (p.Ala81=)	ART3, CXCL10	Single nucleotide variant (synonymous variant +2 more)	not provided	GBenign

ClinVar