"Labcorp Genetics (formerly Invitae), Labcorp"[submitter] AND "TPR"[ge - ClinVar - NCBI

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Items: 16

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2127928	NM_005807.6(PRG4):c.3850del (p.Arg1284fs)	PRG4, TPR (R1241fs +4 more)	Deletion (frameshift variant +1 more)	not provided	GPathogenic
Select item 781667	NM_003292.3(TPR):c.*1711A>G	PRG4, TPR	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign/Likely benign
Select item 732422	NM_003292.3(TPR):c.*1087G>T	PRG4, TPR	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign/Likely benign
Select item 782687	NM_003292.3(TPR):c.6502C>T (p.Pro2168Ser)	TPR (P2168S)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 748541	NM_003292.3(TPR):c.5586C>T (p.Val1862=)	TPR	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 770682	NM_003292.3(TPR):c.5495G>A (p.Arg1832His)	TPR (R1832H)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 778239	NM_003292.3(TPR):c.3942G>A (p.Leu1314=)	TPR	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 755180	NM_003292.3(TPR):c.3720T>C (p.Asp1240=)	TPR	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 727199	NM_003292.3(TPR):c.3675A>G (p.Arg1225=)	TPR	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 708065	NM_003292.3(TPR):c.3443G>A (p.Arg1148His)	LOC126805954, TPR (R1148H)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 715995	NM_003292.3(TPR):c.3116C>T (p.Thr1039Ile)	TPR (T1039I)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 787755	NM_003292.3(TPR):c.2286G>A (p.Thr762=)	TPR	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 748542	NM_003292.3(TPR):c.1941A>G (p.Thr647=)	LOC126805955, TPR	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 770683	NM_003292.3(TPR):c.1399C>A (p.Arg467=)	TPR	Single nucleotide variant (synonymous variant)	not provided	GBenign/Likely benign
Select item 2426819	NC_000001.10:g.(?_185703912)_(186957640_?)dup	HMCN1, OCLM +6 more	Duplication	not provided	GUncertain significance
Select item 1003645	NC_000001.10:g.(?_130980840)_(248900000_?)dup	ARL8A, CNIH4 +956 more	Duplication	Gastrointestinal stromal tumor +2 more	GUncertain significance