"Labcorp Genetics (formerly Invitae), Labcorp"[submitter] AND "LOC1300 - ClinVar - NCBI

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Items: 11

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1367995	NM_016292.3(TRAP1):c.88+1G>A	LOC130058352, TRAP1	Single nucleotide variant (splice donor variant)	not provided	GUncertain significance
Select item 1899064	NM_016292.3(TRAP1):c.65C>G (p.Pro22Arg)	TRAP1, LOC130058352 (P22R)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2961036	NM_016292.3(TRAP1):c.55C>T (p.Leu19=)	LOC130058352, TRAP1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2957041	NM_016292.3(TRAP1):c.48G>A (p.Arg16=)	LOC130058352, TRAP1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 559158	NM_016292.3(TRAP1):c.37C>T (p.Arg13Cys)	LOC130058352, TRAP1 (R13C)	Single nucleotide variant (missense variant)	not specified +1 more	GBenign
Select item 1637502	NM_016292.3(TRAP1):c.28C>T (p.Leu10=)	LOC130058352, TRAP1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1909805	NM_016292.3(TRAP1):c.20C>T (p.Ala7Val)	LOC130058352, TRAP1 (A7V)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1491037	NM_016292.3(TRAP1):c.9C>T (p.Arg3=)	LOC130058352, TRAP1	Single nucleotide variant (synonymous variant)	not provided	GUncertain significance
Select item 1638607	NM_016292.3(TRAP1):c.6G>C (p.Ala2=)	LOC130058352, TRAP1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1518112	NM_016292.3(TRAP1):c.4G>T (p.Ala2Ser)	LOC130058352, TRAP1 (A2S)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 2985801	NM_016292.3(TRAP1):c.3G>A (p.Met1Ile)	LOC130058352, TRAP1 (M1I)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance