SYT15[gene] and "single gene"[properties] - ClinVar - NCBI

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Items: 9

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2370533	NM_031912.5(SYT15):c.22G>A (p.Val8Met)	SYT15 (V8M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2293370	NM_031912.5(SYT15):c.26T>C (p.Ile9Thr)	SYT15 (I9T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2222034	NM_031912.5(SYT15):c.169C>T (p.Arg57Trp)	SYT15 (R57W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3172977	NM_031912.5(SYT15):c.245C>G (p.Thr82Ser)	SYT15 (T82S)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2534010	NM_031912.5(SYT15):c.283G>C (p.Glu95Gln)	SYT15 (E95Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3172978	NM_031912.5(SYT15):c.314C>T (p.Pro105Leu)	SYT15 (P105L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2315315	NM_031912.5(SYT15):c.401T>C (p.Phe134Ser)	SYT15 (F134S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2392072	NM_031912.5(SYT15):c.571C>A (p.Pro191Thr)	SYT15 (P191T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2566519	NM_031912.5(SYT15):c.607C>T (p.Arg203Cys)	SYT15 (R203C)	Single nucleotide variant (missense variant)	not specified	GLikely benign