"PreventionGenetics, part of Exact Sciences"[submitter] AND "SYT14"[ge - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2592327	NM_001146262.4(SYT14):c.8T>C (p.Ile3Thr)	SYT14 (I3T)	Single nucleotide variant (synonymous variant +3 more)	not specified +1 more	GLikely benign
Select item 3047989	NM_001146262.4(SYT14):c.61+13133_61+13134dup	SYT14	Duplication (intron variant)	SYT14-related disorder	GLikely benign
Select item 586694	NM_001146262.4(SYT14):c.285G>A (p.Ala95=)	SYT14	Single nucleotide variant (synonymous variant +1 more)	SYT14-related disorder +1 more	GLikely benign
Select item 586691	NM_001146262.4(SYT14):c.1055G>A (p.Arg352His)	SYT14 (R397H +3 more)	Single nucleotide variant (missense variant)	SYT14-related disorder +1 more	GLikely benign
Select item 716187	NM_001146262.4(SYT14):c.1068A>G (p.Glu356=)	SYT14	Single nucleotide variant (synonymous variant)	SYT14-related disorder +1 more	GBenign/Likely benign
Select item 3035754	NM_001146262.4(SYT14):c.1536A>G (p.Leu512=)	SYT14	Single nucleotide variant (synonymous variant +1 more)	SYT14-related disorder	GLikely benign

ClinVar