CCL5[gene] and "single gene"[properties] - ClinVar

	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 12740	NM_002985.3(CCL5):c.76+231T>C	CCL5	Single nucleotide variant (intron variant)	Human immunodeficiency virus type 1, rapid disease progression with infection by	GPathogenic
Select item 2379782	NM_002985.3(CCL5):c.14C>T (p.Ala5Val)	CCL5 (A5V)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 12739	NC_000017.11:g.35880401G>C	CCL5	Single nucleotide variant	Human immunodeficiency virus type 1, delayed disease progression with infection by	GPathogenic
Select item 395394	GRCh37/hg19 17q12(chr17:34205640-34245061)x3	CCL5	Copy number gain	See cases	GBenign

ClinVar