"Ambry Genetics"[submitter] AND "CXCL6"[gene] - ClinVar - NCBI

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Items: 9

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2252680	NM_002993.4(CXCL6):c.32T>C (p.Val11Ala)	CXCL6, LOC123477759 (V11A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2248884	NM_002993.4(CXCL6):c.62T>A (p.Leu21Gln)	CXCL6, LOC123477759 (L21Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3079186	NM_002993.4(CXCL6):c.86C>T (p.Thr29Met)	CXCL6, LOC123477759 (T29M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3270408	NM_002993.4(CXCL6):c.181A>G (p.Lys61Glu)	CXCL6 (K61E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2217943	NM_002993.4(CXCL6):c.182A>G (p.Lys61Arg)	CXCL6 (K61R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3079185	NM_002993.4(CXCL6):c.223T>C (p.Cys75Arg)	CXCL6 (C75R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2558188	NM_002993.4(CXCL6):c.239T>G (p.Val80Gly)	CXCL6 (V80G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2231198	NM_002993.4(CXCL6):c.295C>G (p.Leu99Val)	CXCL6 (L99V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3270407	NM_002993.4(CXCL6):c.340A>G (p.Asn114Asp)	CXCL6 (N114D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance