"Ambry Genetics"[submitter] AND "SYT6"[gene] - ClinVar

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Items: 28

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3324058	NM_001253772.2(SYT6):c.1526G>A (p.Arg509Gln)	SYT6 (R509Q +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2613569	NM_001253772.2(SYT6):c.1469T>C (p.Ile490Thr)	SYT6 (I490T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2349488	NM_001253772.2(SYT6):c.1421T>C (p.Leu474Pro)	SYT6 (L389P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2340196	NM_001253772.2(SYT6):c.1385T>C (p.Ile462Thr)	SYT6 (I377T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3173025	NM_001253772.2(SYT6):c.1339C>T (p.Leu447Phe)	SYT6 (L362F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3173027	NM_001253772.2(SYT6):c.1229G>T (p.Arg410Leu)	SYT6 (R325L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2387862	NM_001253772.2(SYT6):c.1228C>T (p.Arg410Trp)	SYT6 (R325W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2223340	NM_001253772.2(SYT6):c.1052A>T (p.Asp351Val)	SYT6 (D351V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2616834	NM_001253772.2(SYT6):c.962G>T (p.Arg321Leu)	SYT6 (R236L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2338325	NM_001253772.2(SYT6):c.962G>A (p.Arg321His)	SYT6 (R321H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3324057	NM_001253772.2(SYT6):c.928C>T (p.Arg310Cys)	SYT6 (R225C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2325936	NM_001253772.2(SYT6):c.889A>G (p.Asn297Asp)	SYT6 (N297D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3324056	NM_001253772.2(SYT6):c.830G>A (p.Arg277His)	SYT6 (R277H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2368560	NM_001253772.2(SYT6):c.829C>T (p.Arg277Cys)	SYT6 (R192C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3324053	NM_001253772.2(SYT6):c.792C>A (p.Ser264Arg)	SYT6 (S179R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2485267	NM_001253772.2(SYT6):c.788G>A (p.Gly263Glu)	SYT6 (G263E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2513808	NM_001253772.2(SYT6):c.758C>T (p.Ala253Val)	SYT6 (A253V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2227076	NM_001253772.2(SYT6):c.665C>A (p.Ala222Asp)	SYT6 (A137D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2406490	NM_001253772.2(SYT6):c.608G>A (p.Ser203Asn)	SYT6 (S203N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2207721	NM_001253772.2(SYT6):c.529C>T (p.Arg177Cys)	SYT6 (R177C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3173026	NM_001253772.2(SYT6):c.521C>A (p.Ser174Tyr)	SYT6 (S89Y +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2508550	NM_001253772.2(SYT6):c.481C>T (p.Arg161Trp)	SYT6 (R76W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3324055	NM_001253772.2(SYT6):c.472C>T (p.Arg158Trp)	SYT6 (R158W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2217765	NM_001253772.2(SYT6):c.464G>A (p.Arg155His)	SYT6 (R155H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3324054	NM_001253772.2(SYT6):c.457A>T (p.Ile153Phe)	SYT6 (I68F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3324052	NM_001253772.2(SYT6):c.440T>C (p.Met147Thr)	SYT6 (M62T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2223448	NM_001253772.2(SYT6):c.440T>A (p.Met147Lys)	SYT6 (M62K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2454459	NM_001253772.2(SYT6):c.304C>T (p.Pro102Ser)	SYT6 (P102S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 28