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

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 376558	NM_005648.4(ELOC):c.236A>T (p.Tyr79Phe)	ELOC (Y63F +1 more)	Single nucleotide variant (missense variant)	Papillary renal cell carcinoma type 1	GLikely pathogenic
Select item 376556	NM_005648.4(ELOC):c.236A>C (p.Tyr79Ser)	ELOC (Y63S +1 more)	Single nucleotide variant (missense variant)	Papillary renal cell carcinoma type 1	GLikely pathogenic
Select item 376557	NM_005648.4(ELOC):c.235T>A (p.Tyr79Asn)	ELOC (Y63N +1 more)	Single nucleotide variant (missense variant)	Papillary renal cell carcinoma type 1	GLikely pathogenic
Select item 3088460	NM_005648.4(ELOC):c.64A>C (p.Ile22Leu)	ELOC (I22L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3275216	NM_005648.4(ELOC):c.61T>G (p.Leu21Val)	ELOC (L21V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3088459	NM_005648.4(ELOC):c.10G>A (p.Glu4Lys)	ELOC (E4K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

ClinVar