"Ambry Genetics"[submitter] AND "CCL5"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2380266	NM_002985.3(CCL5):c.119G>A (p.Arg40His)	CCL5 (R40H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3139752	NM_002985.3(CCL5):c.88A>G (p.Thr30Ala)	CCL5 (T30A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2379782	NM_002985.3(CCL5):c.14C>T (p.Ala5Val)	CCL5 (A5V)	Single nucleotide variant (missense variant)	not specified	GLikely benign

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