CCL28[gene] and "single gene"[properties] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2353839	NM_148672.3(CCL28):c.341A>G (p.His114Arg)	CCL28 (H114R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2216565	NM_148672.3(CCL28):c.317G>T (p.Gly106Val)	CCL28 (G106V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2525172	NM_148672.3(CCL28):c.206G>T (p.Arg69Leu)	CCL28 (R22L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3139747	NM_148672.3(CCL28):c.175G>A (p.Asp59Asn)	CCL28 (D12N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2229576	NM_148672.3(CCL28):c.143T>A (p.Met48Lys)	CCL28 (M1K +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2334009	NM_148672.3(CCL28):c.136G>C (p.Val46Leu)	CCL28 (V46L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3139748	NM_148672.3(CCL28):c.38T>A (p.Val13Asp)	CCL28 (V13D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

ClinVar