Related gene-specific medical variations for Gene (Select 6373) - ClinVar - NCBI

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Items: 5

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2591156	NM_005409.5(CXCL11):c.190A>G (p.Ile64Val)	ART3, CXCL11 (I64V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2528238	NM_005409.5(CXCL11):c.234A>C (p.Lys78Asn)	ART3, CXCL11 (K78N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2494248	NM_005409.5(CXCL11):c.263A>C (p.Lys88Thr)	ART3, CXCL11 (K88T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2409509	NM_005409.5(CXCL11):c.59A>C (p.Gln20Pro)	ART3, CXCL11 (Q20P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2229108	NM_005409.5(CXCL11):c.242A>T (p.Gln81Leu)	ART3, CXCL11 (Q81L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

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