"Labcorp Genetics (formerly Invitae), Labcorp"[submitter] AND "SNAP91" - ClinVar - NCBI

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Items: 10

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 778343	NM_001242792.2(SNAP91):c.2508T>C (p.Pro836=)	SNAP91	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign/Likely benign
Select item 713594	NM_001242792.2(SNAP91):c.2496G>A (p.Ser832=)	SNAP91	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 737562	NM_001242792.2(SNAP91):c.2113C>T (p.Pro705Ser)	SNAP91 (P614S +20 more)	Single nucleotide variant (missense variant +1 more)	not provided	GBenign
Select item 787305	NM_001242792.2(SNAP91):c.2058T>G (p.Thr686=)	SNAP91	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 730681	NM_001242792.2(SNAP91):c.1446G>A (p.Pro482=)	SNAP91	Single nucleotide variant (synonymous variant +2 more)	not provided	GBenign
Select item 792043	NM_001242792.2(SNAP91):c.1157-3T>C	SNAP91	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 720306	NM_001242792.2(SNAP91):c.1142-6C>G	SNAP91	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 735398	NM_001242792.2(SNAP91):c.495A>G (p.Leu165=)	SNAP91	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 780642	NM_001242792.2(SNAP91):c.18C>G (p.Leu6=)	SNAP91	Single nucleotide variant (synonymous variant +2 more)	not provided	GBenign
Select item 1003195	NC_000006.11:g.(?_83878953)_(84567108_?)dup	ME1, PGM3 +4 more	Duplication	not provided	GUncertain significance