ClinVar for Gene (Select 348249) - ClinVar - NCBI

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Links from Gene

Items: 14

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3264463	NM_032963.4(CCL14):c.172C>A (p.Gln58Lys)	CCL14, CCL15-CCL14 (Q74K +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3139713	NM_032965.6(CCL15):c.98T>C (p.Met33Thr)	CCL15, CCL15-CCL14 (M33T)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3139712	NM_032963.4(CCL14):c.187G>A (p.Gly63Arg)	CCL14, CCL15-CCL14 (G63R +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3139711	NM_032963.4(CCL14):c.176G>A (p.Cys59Tyr)	CCL14, CCL15-CCL14 (C75Y +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3139710	NM_032963.4(CCL14):c.13G>A (p.Val5Met)	CCL14, CCL15-CCL14 (V5M)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GLikely benign
Select item 2359035	NM_032963.4(CCL14):c.83G>A (p.Gly28Glu)	CCL14, CCL15-CCL14 (G28E +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2335190	NM_032965.6(CCL15):c.337A>G (p.Ile113Val)	CCL15, CCL15-CCL14 (I113V)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2327723	NM_032965.6(CCL15):c.13G>A (p.Val5Met)	CCL15, CCL15-CCL14 (V5M)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2324454	NM_032965.6(CCL15):c.316A>C (p.Lys106Gln)	CCL15, CCL15-CCL14 (K106Q)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2318233	NM_032965.6(CCL15):c.268C>T (p.Arg90Trp)	CCL15, CCL15-CCL14 (R90W)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2295803	NM_032965.6(CCL15):c.338T>C (p.Ile113Thr)	CCL15, CCL15-CCL14 (I113T)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2254496	NM_032965.6(CCL15):c.203A>G (p.Lys68Arg)	CCL15, CCL15-CCL14 (K68R)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2250969	NM_032965.6(CCL15):c.269G>A (p.Arg90Gln)	CCL15, CCL15-CCL14 (R90Q)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GLikely benign
Select item 58166	GRCh37/hg19 17q12(chr17:34310998-36297053)x3	AATF, ACACA +48 more	Copy number gain	See cases	GPathogenic