ClinVar Miner

List of variants in gene SZT2 reported as uncertain significance for Seizures

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Total variants: 56
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HGVS dbSNP
NM_001365999.1(SZT2):c.-4T>C
NM_001365999.1(SZT2):c.10288C>T (p.Arg3430Cys)
NM_001365999.1(SZT2):c.1060G>T (p.Gly354Trp) rs1557539813
NM_001365999.1(SZT2):c.137C>T (p.Thr46Ile)
NM_001365999.1(SZT2):c.1385C>T (p.Thr462Met)
NM_001365999.1(SZT2):c.2014A>T (p.Thr672Ser)
NM_001365999.1(SZT2):c.2228A>G (p.His743Arg)
NM_001365999.1(SZT2):c.2282G>A (p.Arg761Gln)
NM_001365999.1(SZT2):c.2315G>A (p.Gly772Asp) rs1557550662
NM_001365999.1(SZT2):c.2545A>G (p.Ile849Val)
NM_001365999.1(SZT2):c.2646-3T>C
NM_001365999.1(SZT2):c.2747G>A (p.Arg916Gln)
NM_001365999.1(SZT2):c.2787C>G (p.Asp929Glu)
NM_001365999.1(SZT2):c.2824C>T (p.Arg942Trp)
NM_001365999.1(SZT2):c.2825G>A (p.Arg942Gln)
NM_001365999.1(SZT2):c.2887A>G (p.Lys963Glu)
NM_001365999.1(SZT2):c.2930-5C>T
NM_001365999.1(SZT2):c.3916C>T (p.Arg1306Cys)
NM_001365999.1(SZT2):c.4049C>T (p.Thr1350Ile)
NM_001365999.1(SZT2):c.4064A>G (p.His1355Arg) rs149741610
NM_001365999.1(SZT2):c.4343G>A (p.Arg1448His)
NM_001365999.1(SZT2):c.4480+4T>C
NM_001365999.1(SZT2):c.4721G>A (p.Arg1574Gln) rs532357677
NM_001365999.1(SZT2):c.4765A>C (p.Thr1589Pro) rs1348292126
NM_001365999.1(SZT2):c.4814G>T (p.Gly1605Val)
NM_001365999.1(SZT2):c.4972T>A (p.Leu1658Ile)
NM_001365999.1(SZT2):c.5072A>C (p.Glu1691Ala)
NM_001365999.1(SZT2):c.5284C>T (p.Arg1762Cys)
NM_001365999.1(SZT2):c.5515C>T (p.Arg1839Cys) rs147748994
NM_001365999.1(SZT2):c.5551C>T (p.Arg1851Trp)
NM_001365999.1(SZT2):c.5552G>A (p.Arg1851Gln)
NM_001365999.1(SZT2):c.559T>C (p.Tyr187His)
NM_001365999.1(SZT2):c.5876T>C (p.Val1959Ala)
NM_001365999.1(SZT2):c.6008G>A (p.Arg2003His)
NM_001365999.1(SZT2):c.6038A>G (p.Tyr2013Cys)
NM_001365999.1(SZT2):c.6077C>A (p.Ala2026Glu)
NM_001365999.1(SZT2):c.6185G>A (p.Arg2062Gln)
NM_001365999.1(SZT2):c.6335C>T (p.Ala2112Val)
NM_001365999.1(SZT2):c.670C>G (p.Arg224Gly)
NM_001365999.1(SZT2):c.6977G>A (p.Arg2326Gln)
NM_001365999.1(SZT2):c.7474C>T (p.Arg2492Trp)
NM_001365999.1(SZT2):c.7513C>T (p.Arg2505Cys)
NM_001365999.1(SZT2):c.7816C>T (p.Arg2606Trp)
NM_001365999.1(SZT2):c.7873+5G>A
NM_001365999.1(SZT2):c.8137G>A (p.Val2713Met)
NM_001365999.1(SZT2):c.8255G>A (p.Arg2752His) rs150591561
NM_001365999.1(SZT2):c.847C>T (p.Arg283Cys) rs1557534581
NM_001365999.1(SZT2):c.8702C>T (p.Pro2901Leu) rs139027171
NM_001365999.1(SZT2):c.8930C>T (p.Pro2977Leu)
NM_001365999.1(SZT2):c.9049A>G (p.Met3017Val)
NM_001365999.1(SZT2):c.9072+4T>C
NM_001365999.1(SZT2):c.9460T>C (p.Ser3154Pro) rs1271549438
NM_001365999.1(SZT2):c.9665C>T (p.Pro3222Leu)
NM_001365999.1(SZT2):c.9781C>T (p.Arg3261Trp)
NM_001365999.1(SZT2):c.9880C>T (p.Arg3294Trp)
NM_001365999.1(SZT2):c.9931G>T (p.Val3311Phe) rs1557606189

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