"Labcorp Genetics (formerly Invitae), Labcorp"[submitter] AND "NRP2"[g - ClinVar

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Items: 29

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 789973	NM_003872.3(NRP2):c.123C>T (p.Thr41=)	NRP2	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 791470	NM_003872.3(NRP2):c.180C>T (p.Tyr60=)	NRP2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 769578	NM_003872.3(NRP2):c.368A>G (p.Lys123Arg)	NRP2 (K123R)	Single nucleotide variant (missense variant)	not specified +1 more	GBenign
Select item 761015	NM_003872.3(NRP2):c.387C>A (p.Ala129=)	NRP2	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 744147	NM_003872.3(NRP2):c.420G>A (p.Glu140=)	NRP2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 721609	NM_003872.3(NRP2):c.559A>G (p.Ile187Val)	NRP2 (I187V)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 775807	NM_003872.3(NRP2):c.726G>A (p.Thr242=)	NRP2	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 792930	NM_003872.3(NRP2):c.762G>A (p.Ala254=)	NRP2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 717718	NM_003872.3(NRP2):c.838C>T (p.Pro280Ser)	NRP2 (P280S)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 791885	NM_003872.3(NRP2):c.860G>A (p.Arg287Gln)	NRP2 (R287Q)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 729740	NM_003872.3(NRP2):c.962A>T (p.Asn321Ile)	NRP2 (N321I)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 756039	NM_003872.3(NRP2):c.996C>T (p.Asp332=)	NRP2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 781825	NM_003872.3(NRP2):c.1146+7C>T	NRP2	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 782419	NM_003872.3(NRP2):c.1149A>G (p.Val383=)	NRP2	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 717896	NM_003872.3(NRP2):c.1333A>C (p.Ile445Leu)	NRP2 (I445L)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 777569	NM_003872.3(NRP2):c.1404= (p.Val468=)	NRP2	Variation (no sequence alteration)	not provided	GBenign
Select item 737189	NM_003872.3(NRP2):c.1416G>A (p.Ser472=)	NRP2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 724326	NM_003872.3(NRP2):c.1449C>T (p.Pro483=)	NRP2	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 794116	NM_003872.3(NRP2):c.1719A>G (p.Val573=)	NRP2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 789562	NM_003872.3(NRP2):c.1737G>A (p.Ser579=)	NRP2	Single nucleotide variant (synonymous variant)	not provided	GBenign/Likely benign
Select item 789563	NM_003872.3(NRP2):c.1800G>A (p.Thr600=)	NRP2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 738629	NM_003872.3(NRP2):c.1831G>A (p.Glu611Lys)	NRP2 (E611K)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 741818	NM_003872.3(NRP2):c.1953C>T (p.Leu651=)	LOC126806481, NRP2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 761746	NM_003872.3(NRP2):c.2316C>T (p.Phe772=)	NRP2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 750432	NM_003872.3(NRP2):c.2425+24A>T	NRP2	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 69499	NM_003872.3(NRP2):c.2568C>T (p.Thr856=)	NRP2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 744614	NM_003872.3(NRP2):c.2649C>T (p.Leu883=)	NRP2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 719903	NM_003872.3(NRP2):c.2679C>T (p.Ser893=)	NRP2	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 1511552	NC_000002.11:g.(?_203420070)_(211811277_?)del	ABI2, ACADL +44 more	Deletion	Primary pulmonary hypertension	GUncertain significance

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Items: 29