Related gene-specific medical variations for Gene (Select 284340) - ClinVar - NCBI

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Items: 5

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3079177	NM_198477.3(CXCL17):c.85G>A (p.Ala29Thr)	CXCL17, LIPE-AS1 (A29T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3079176	NM_198477.3(CXCL17):c.65G>C (p.Ser22Thr)	CXCL17, LIPE-AS1 (S22T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2404158	NM_198477.3(CXCL17):c.149G>C (p.Cys50Ser)	CXCL17, LIPE-AS1 (C50S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2289173	NM_198477.3(CXCL17):c.263G>A (p.Arg88Lys)	CXCL17, LIPE-AS1 (R88K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 719830	NM_198477.3(CXCL17):c.54C>T (p.Ser18=)	CXCL17, LIPE-AS1	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign

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