ClinVar Miner

List of variants in gene SZT2 reported by Ambry Genetics

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 133
Download table as spreadsheet
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.1272A>G (p.Gln424=) rs780157180
NM_001365999.1(SZT2):c.1296G>A (p.Leu432=)
NM_001365999.1(SZT2):c.1335A>T (p.Ala445=)
NM_001365999.1(SZT2):c.1336C>T (p.Pro446Ser) rs2782643
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.2034C>T (p.His678=)
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.2427G>A (p.Ala809=)
NM_001365999.1(SZT2):c.2499C>T (p.Phe833=)
NM_001365999.1(SZT2):c.2545A>G (p.Ile849Val)
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.2631C>T (p.Thr877=) rs140831372
NM_001365999.1(SZT2):c.2646-3T>C
NM_001365999.1(SZT2):c.2747G>A (p.Arg916Gln)
NM_001365999.1(SZT2):c.2775G>A (p.Lys925=)
NM_001365999.1(SZT2):c.2787C>G (p.Asp929Glu)
NM_001365999.1(SZT2):c.2788C>T (p.Leu930=)
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.2955C>T (p.Cys985=) rs151189395
NM_001365999.1(SZT2):c.297G>A (p.Glu99=)
NM_001365999.1(SZT2):c.3251C>T (p.Pro1084Leu)
NM_001365999.1(SZT2):c.3267C>T (p.Val1089=) rs147008168
NM_001365999.1(SZT2):c.3297T>C (p.Ala1099=) rs1557557255
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.3690G>A (p.Ala1230=)
NM_001365999.1(SZT2):c.3782C>T (p.Ala1261Val)
NM_001365999.1(SZT2):c.3916C>T (p.Arg1306Cys)
NM_001365999.1(SZT2):c.4049C>T (p.Thr1350Ile)
NM_001365999.1(SZT2):c.4051T>C (p.Trp1351Arg) rs72883814
NM_001365999.1(SZT2):c.4064A>G (p.His1355Arg) rs149741610
NM_001365999.1(SZT2):c.4176C>T (p.Thr1392=) rs373047934
NM_001365999.1(SZT2):c.4343G>A (p.Arg1448His)
NM_001365999.1(SZT2):c.4480+4T>C
NM_001365999.1(SZT2):c.4524G>A (p.Glu1508=)
NM_001365999.1(SZT2):c.4525C>T (p.Leu1509=) rs1557566670
NM_001365999.1(SZT2):c.4531G>A (p.Val1511Ile) rs76675748
NM_001365999.1(SZT2):c.4599C>T (p.Asp1533=)
NM_001365999.1(SZT2):c.4701G>A (p.Leu1567=)
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.4898C>T (p.Ser1633Leu)
NM_001365999.1(SZT2):c.4972T>A (p.Leu1658Ile)
NM_001365999.1(SZT2):c.4983T>C (p.Asp1661=) rs139810154
NM_001365999.1(SZT2):c.5072A>C (p.Glu1691Ala)
NM_001365999.1(SZT2):c.5075C>T (p.Thr1692Ile) rs149831634
NM_001365999.1(SZT2):c.5198G>A (p.Arg1733His) rs147797700
NM_001365999.1(SZT2):c.5284C>T (p.Arg1762Cys)
NM_001365999.1(SZT2):c.5385T>G (p.Ser1795=) rs12129487
NM_001365999.1(SZT2):c.5515C>T (p.Arg1839Cys) rs147748994
NM_001365999.1(SZT2):c.5516G>A (p.Arg1839His) rs760427137
NM_001365999.1(SZT2):c.5517C>T (p.Arg1839=) rs147753139
NM_001365999.1(SZT2):c.5535T>G (p.Ser1845Arg) rs114759137
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.603G>A (p.Leu201=) rs1557531678
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.6380A>T (p.Tyr2127Phe) rs149812437
NM_001365999.1(SZT2):c.6541C>T (p.Leu2181=)
NM_001365999.1(SZT2):c.6543A>G (p.Leu2181=) rs112461557
NM_001365999.1(SZT2):c.6573C>T (p.Asp2191=)
NM_001365999.1(SZT2):c.670C>G (p.Arg224Gly)
NM_001365999.1(SZT2):c.675G>A (p.Lys225=)
NM_001365999.1(SZT2):c.6888C>T (p.Cys2296=) rs72671125
NM_001365999.1(SZT2):c.6977G>A (p.Arg2326Gln)
NM_001365999.1(SZT2):c.7069T>C (p.Leu2357=)
NM_001365999.1(SZT2):c.7149C>T (p.Ala2383=)
NM_001365999.1(SZT2):c.7224C>T (p.Asn2408=)
NM_001365999.1(SZT2):c.7256G>A (p.Arg2419Gln) rs72637949
NM_001365999.1(SZT2):c.7356A>G (p.Glu2452=) rs2027130
NM_001365999.1(SZT2):c.7395T>C (p.Ile2465=) rs78858677
NM_001365999.1(SZT2):c.7446G>A (p.Glu2482=)
NM_001365999.1(SZT2):c.7474C>T (p.Arg2492Trp)
NM_001365999.1(SZT2):c.7512-3C>T rs117106532
NM_001365999.1(SZT2):c.7513C>T (p.Arg2505Cys)
NM_001365999.1(SZT2):c.7562T>C (p.Val2521Ala) rs150113647
NM_001365999.1(SZT2):c.7573G>A (p.Val2525Ile) rs139486476
NM_001365999.1(SZT2):c.759G>A (p.Ser253=) rs1889586
NM_001365999.1(SZT2):c.7641C>T (p.His2547=)
NM_001365999.1(SZT2):c.7816C>T (p.Arg2606Trp)
NM_001365999.1(SZT2):c.7831C>T (p.Leu2611=)
NM_001365999.1(SZT2):c.7873+5G>A
NM_001365999.1(SZT2):c.7896C>T (p.Phe2632=)
NM_001365999.1(SZT2):c.8020T>C (p.Leu2674=) rs187106999
NM_001365999.1(SZT2):c.8136C>T (p.Pro2712=) rs2275098
NM_001365999.1(SZT2):c.8137G>A (p.Val2713Met)
NM_001365999.1(SZT2):c.8177C>G (p.Thr2726Ser) rs145882968
NM_001365999.1(SZT2):c.8255G>A (p.Arg2752His) rs150591561
NM_001365999.1(SZT2):c.8295C>T (p.Asp2765=)
NM_001365999.1(SZT2):c.8459C>T (p.Thr2820Ile) rs776178283
NM_001365999.1(SZT2):c.847C>T (p.Arg283Cys) rs1557534581
NM_001365999.1(SZT2):c.8568C>T (p.Phe2856=)
NM_001365999.1(SZT2):c.8626-3T>C rs2255632
NM_001365999.1(SZT2):c.8702C>T (p.Pro2901Leu) rs139027171
NM_001365999.1(SZT2):c.8782G>A (p.Gly2928Ser) rs765828066
NM_001365999.1(SZT2):c.8910C>T (p.Ser2970=) rs116536134
NM_001365999.1(SZT2):c.8930C>T (p.Pro2977Leu)
NM_001365999.1(SZT2):c.8947C>T (p.Leu2983=)
NM_001365999.1(SZT2):c.9049A>G (p.Met3017Val)
NM_001365999.1(SZT2):c.9072+4T>C
NM_001365999.1(SZT2):c.9292T>C (p.Leu3098=)
NM_001365999.1(SZT2):c.9426G>A (p.Val3142=) rs1328052292
NM_001365999.1(SZT2):c.9460T>C (p.Ser3154Pro) rs1271549438
NM_001365999.1(SZT2):c.9576C>T (p.Phe3192=)
NM_001365999.1(SZT2):c.9665C>T (p.Pro3222Leu)
NM_001365999.1(SZT2):c.9723G>A (p.Ala3241=) rs146635122
NM_001365999.1(SZT2):c.9732G>A (p.Pro3244=)
NM_001365999.1(SZT2):c.9781C>T (p.Arg3261Trp)
NM_001365999.1(SZT2):c.9782G>A (p.Arg3261Gln)
NM_001365999.1(SZT2):c.9828C>T (p.Asp3276=)
NM_001365999.1(SZT2):c.9880C>T (p.Arg3294Trp)
NM_001365999.1(SZT2):c.9883C>T (p.Leu3295=)
NM_001365999.1(SZT2):c.9931G>T (p.Val3311Phe) rs1557606189

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.