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

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Items: 16

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 713115	NM_001831.4(CLU):c.1314G>T (p.Ala438=)	CLU	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 734907	NM_001831.4(CLU):c.1191C>T (p.Asp397=)	CLU	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 716148	NM_001831.4(CLU):c.1187C>T (p.Ser396Leu)	CLU (S396L)	Single nucleotide variant (missense variant +1 more)	not provided	GBenign
Select item 739758	NM_001831.4(CLU):c.999C>T (p.Val333=)	CLU	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 788866	NM_001831.4(CLU):c.984C>T (p.Asp328=)	CLU	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 776303	NM_001831.4(CLU):c.982G>A (p.Asp328Asn)	CLU (D328N)	Single nucleotide variant (missense variant +1 more)	not provided	GBenign
Select item 776304	NM_001831.4(CLU):c.954C>G (p.Pro318=)	CLU	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 729718	NM_001831.4(CLU):c.756C>T (p.His252=)	CLU	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 799508	NM_001831.4(CLU):c.705C>T (p.Tyr235=)	CLU	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 428612	NM_001831.4(CLU):c.608C>T (p.Thr203Ile)	CLU (T203I)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 745644	NM_001831.4(CLU):c.564C>T (p.Asp188=)	CLU	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 748692	NM_001831.4(CLU):c.417+8G>C	CLU	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 726773	NM_001831.4(CLU):c.382G>A (p.Val128Ile)	CLU (V128I)	Single nucleotide variant (missense variant +1 more)	not provided	GBenign
Select item 715615	NM_001831.4(CLU):c.123C>T (p.Tyr41=)	CLU	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 791273	NM_001831.4(CLU):c.75G>A (p.Thr25=)	CLU	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 1511682	NC_000008.10:g.(?_27319146)_(28608383_?)dup	CCDC25, CHRNA2 +13 more	Duplication	Autosomal dominant nocturnal frontal lobe epilepsy	GUncertain significance