"Invitae"[submitter] AND "RASAL2"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 721721	NM_170692.4(RASAL2):c.83C>A (p.Pro28Gln)	RASAL2 (P28Q)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 719624	NM_170692.4(RASAL2):c.834C>T (p.Thr278=)	RASAL2	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 723880	NM_170692.4(RASAL2):c.1107T>C (p.Leu369=)	RASAL2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 709358	NM_170692.4(RASAL2):c.1299G>A (p.Arg433=)	RASAL2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 723881	NM_170692.4(RASAL2):c.2541C>T (p.Ser847=)	RASAL2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 769545	NM_170692.4(RASAL2):c.3132G>C (p.Val1044=)	RASAL2	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 1003645	NC_000001.10:g.(?_130980840)_(248900000_?)dup	KLHL12, LNCATV +956 more	Duplication	Paragangliomas 3 +2 more	GUncertain significance

ClinVar