"CeGaT Center for Human Genetics Tuebingen"[submitter] AND "SYTL2"[gen - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2642240	NM_206927.4(SYTL2):c.6006C>T (p.Asn2002=)	SYTL2	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2642241	NM_206927.4(SYTL2):c.5746-7C>T	SYTL2	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2642242	NM_206927.4(SYTL2):c.4641A>G (p.Leu1547=)	SYTL2	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2642243	NM_206927.4(SYTL2):c.2535C>A (p.Asp845Glu)	SYTL2 (D817E +3 more)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 2642244	NM_206927.4(SYTL2):c.2213G>C (p.Gly738Ala)	SYTL2 (G710A +3 more)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 2642245	NM_206927.4(SYTL2):c.2130A>G (p.Ser710=)	SYTL2	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2642246	NM_206927.4(SYTL2):c.1960A>G (p.Lys654Glu)	SYTL2 (K626E +3 more)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign

ClinVar