"Labcorp Genetics (formerly Invitae), Labcorp"[submitter] AND "GARIN4" - ClinVar - NCBI

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Items: 5

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 767746	NM_153606.4(GARIN4):c.873C>G (p.Thr291=)	GARIN4	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 767747	NM_153606.4(GARIN4):c.1071C>T (p.Ser357=)	GARIN4	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 710838	NM_153606.4(GARIN4):c.1663A>T (p.Lys555Ter)	GARIN4 (K555*)	Single nucleotide variant (nonsense)	not provided	GLikely benign
Select item 3248093	NC_000001.10:g.(?_190829412)_(216061974_?)del	RPS6KC1, SERTAD4 +185 more	Deletion	not provided	GPathogenic
Select item 1003645	NC_000001.10:g.(?_130980840)_(248900000_?)dup	ARL8A, CNIH4 +956 more	Duplication	Gastrointestinal stromal tumor +2 more	GUncertain significance

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