"Labcorp Genetics (formerly Invitae), Labcorp"[submitter] AND "PTK2"[g - ClinVar - NCBI

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Items: 17

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 731408	NM_001352702.2(PTK2):c.2967C>T (p.Ala989=)	PTK2	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 742240	NM_001352702.2(PTK2):c.2923C>T (p.Leu975=)	PTK2	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 714382	NM_001352702.2(PTK2):c.2907C>T (p.Tyr969=)	PTK2	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 787622	NM_001352702.2(PTK2):c.2610G>A (p.Glu870=)	PTK2	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign/Likely benign
Select item 786128	NM_001352702.2(PTK2):c.2467G>A (p.Ala823Thr)	PTK2 (A661T +27 more)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 709439	NM_001352702.2(PTK2):c.2322A>C (p.Pro774=)	PTK2	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 785268	NM_001352702.2(PTK2):c.2109C>T (p.Asp703=)	PTK2	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 717392	NM_001352702.2(PTK2):c.2070T>C (p.Pro690=)	PTK2	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 751734	NM_001352702.2(PTK2):c.1584T>A (p.Ile528=)	PTK2	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 760994	NM_001352702.2(PTK2):c.1302T>A (p.Ile434=)	PTK2	Single nucleotide variant (synonymous variant +2 more)	not provided	GLikely benign
Select item 754438	NM_001352702.2(PTK2):c.1161C>T (p.His387=)	PTK2	Single nucleotide variant (synonymous variant +2 more)	not provided	GLikely benign
Select item 785269	NM_001352702.2(PTK2):c.1065G>A (p.Ser355=)	PTK2	Single nucleotide variant (synonymous variant +2 more)	not provided	GBenign
Select item 789195	NM_001352702.2(PTK2):c.1047G>T (p.Arg349=)	PTK2	Single nucleotide variant (synonymous variant +2 more)	not provided	GBenign
Select item 784075	NM_001352702.2(PTK2):c.915A>C (p.Ser305=)	PTK2	Single nucleotide variant (synonymous variant +3 more)	not provided	GLikely benign
Select item 769746	NM_001352702.2(PTK2):c.645C>T (p.Val215=)	PTK2	Single nucleotide variant (synonymous variant +2 more)	not provided	GBenign
Select item 739087	NM_001352702.2(PTK2):c.309C>T (p.Gly103=)	PTK2	Single nucleotide variant (synonymous variant +3 more)	not provided	GLikely benign
Select item 716661	NM_001352702.2(PTK2):c.-18C>T	PTK2	Single nucleotide variant (5 prime UTR variant +3 more)	not provided	GBenign