ClinVar Miner

List of variants in gene SZT2 reported as benign for Seizures

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Total variants: 20
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HGVS dbSNP
NM_001365999.1(SZT2):c.1336C>T (p.Pro446Ser) rs2782643
NM_001365999.1(SZT2):c.2550+5G>A rs41270349
NM_001365999.1(SZT2):c.2550+5G>T rs41270349
NM_001365999.1(SZT2):c.2578G>A (p.Glu860Lys) rs143992266
NM_001365999.1(SZT2):c.3469C>T (p.Pro1157Ser) rs150966402
NM_001365999.1(SZT2):c.348C>A (p.Ile116=) rs41312024
NM_001365999.1(SZT2):c.3582T>C (p.Ser1194=) rs140788949
NM_001365999.1(SZT2):c.4051T>C (p.Trp1351Arg) rs72883814
NM_001365999.1(SZT2):c.4898C>T (p.Ser1633Leu)
NM_001365999.1(SZT2):c.5198G>A (p.Arg1733His) rs147797700
NM_001365999.1(SZT2):c.5385T>G (p.Ser1795=) rs12129487
NM_001365999.1(SZT2):c.5535T>G (p.Ser1845Arg) rs114759137
NM_001365999.1(SZT2):c.6573C>T (p.Asp2191=)
NM_001365999.1(SZT2):c.6888C>T (p.Cys2296=) rs72671125
NM_001365999.1(SZT2):c.7356A>G (p.Glu2452=) rs2027130
NM_001365999.1(SZT2):c.8136C>T (p.Pro2712=) rs2275098
NM_001365999.1(SZT2):c.8177C>G (p.Thr2726Ser) rs145882968
NM_001365999.1(SZT2):c.8626-3T>C rs2255632
NM_001365999.1(SZT2):c.8910C>T (p.Ser2970=) rs116536134
NM_001365999.1(SZT2):c.9782G>A (p.Arg3261Gln)

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