Related gene-specific medical variations for Gene (Select 10663) - ClinVar - NCBI

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Items: 12

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3270429	NM_006564.2(CXCR6):c.85T>A (p.Phe29Ile)	CXCR6, FYCO1 (F29I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3079221	NM_006564.2(CXCR6):c.938G>A (p.Gly313Glu)	CXCR6, FYCO1 (G313E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3079220	NM_006564.2(CXCR6):c.625G>A (p.Val209Ile)	CXCR6, FYCO1 (V209I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3079219	NM_006564.2(CXCR6):c.281A>G (p.Glu94Gly)	CXCR6, FYCO1 (E94G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2619529	NM_006564.2(CXCR6):c.760C>T (p.Arg254Cys)	CXCR6, FYCO1 (R254C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2377362	NM_006564.2(CXCR6):c.197C>T (p.Thr66Met)	CXCR6, FYCO1 (T66M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2354599	NM_006564.2(CXCR6):c.320G>A (p.Gly107Asp)	CXCR6, FYCO1 (G107D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2321431	NM_006564.2(CXCR6):c.847C>T (p.Leu283Phe)	CXCR6, FYCO1 (L283F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2307387	NM_006564.2(CXCR6):c.1009A>C (p.Thr337Pro)	CXCR6, FYCO1 (T337P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 771134	NM_006564.2(CXCR6):c.552C>T (p.Asp184=)	CXCR6, FYCO1	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 756060	NM_006564.2(CXCR6):c.231C>T (p.Asp77=)	CXCR6, FYCO1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 716101	NM_006564.2(CXCR6):c.702C>T (p.Phe234=)	CXCR6, FYCO1	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign