CN263289[trait identifier] AND "Fulgent Genetics, Fulgent Genetics"[su - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 956988	NM_000127.3(EXT1):c.1873A>G (p.Ile625Val)	EXT1 (I625V)	Single nucleotide variant (missense variant)	Chondrosarcoma +2 more	GUncertain significance
Select item 716284	NM_000127.3(EXT1):c.1839G>A (p.Thr613=)	EXT1	Single nucleotide variant (synonymous variant)	Exostoses, multiple, type 1 +2 more	GLikely benign
Select item 279804	NM_000127.3(EXT1):c.1468dup (p.Leu490fs)	EXT1 (L490fs)	Duplication (frameshift variant)	Exostoses, multiple, type 1 +3 more	GPathogenic
Select item 265339	NM_000127.3(EXT1):c.538_539del (p.Leu181fs)	EXT1 (L181fs)	Microsatellite (frameshift variant)	not provided +3 more	GPathogenic
Select item 304577	NM_207122.2(EXT2):c.519G>C (p.Ala173=)	EXT2	Single nucleotide variant (synonymous variant)	Exostoses, multiple, type 2 +3 more	GBenign/Likely benign
Select item 304585	NM_207122.2(EXT2):c.1017T>C (p.Cys339=)	EXT2	Single nucleotide variant (synonymous variant)	Exostoses, multiple, type 2 +3 more	GBenign/Likely benign

ClinVar