ClinVar Miner

List of variants in gene SZT2 reported as likely benign by Ambry Genetics

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Gene type:
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Total variants: 54
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HGVS dbSNP
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.2034C>T (p.His678=)
NM_001365999.1(SZT2):c.2427G>A (p.Ala809=)
NM_001365999.1(SZT2):c.2499C>T (p.Phe833=)
NM_001365999.1(SZT2):c.2631C>T (p.Thr877=) rs140831372
NM_001365999.1(SZT2):c.2775G>A (p.Lys925=)
NM_001365999.1(SZT2):c.2788C>T (p.Leu930=)
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.3690G>A (p.Ala1230=)
NM_001365999.1(SZT2):c.3782C>T (p.Ala1261Val)
NM_001365999.1(SZT2):c.4176C>T (p.Thr1392=) rs373047934
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.4983T>C (p.Asp1661=) rs139810154
NM_001365999.1(SZT2):c.5075C>T (p.Thr1692Ile) rs149831634
NM_001365999.1(SZT2):c.5517C>T (p.Arg1839=) rs147753139
NM_001365999.1(SZT2):c.603G>A (p.Leu201=) rs1557531678
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.675G>A (p.Lys225=)
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.7395T>C (p.Ile2465=) rs78858677
NM_001365999.1(SZT2):c.7446G>A (p.Glu2482=)
NM_001365999.1(SZT2):c.7512-3C>T rs117106532
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.7831C>T (p.Leu2611=)
NM_001365999.1(SZT2):c.7896C>T (p.Phe2632=)
NM_001365999.1(SZT2):c.8020T>C (p.Leu2674=) rs187106999
NM_001365999.1(SZT2):c.8295C>T (p.Asp2765=)
NM_001365999.1(SZT2):c.8568C>T (p.Phe2856=)
NM_001365999.1(SZT2):c.8947C>T (p.Leu2983=)
NM_001365999.1(SZT2):c.9292T>C (p.Leu3098=)
NM_001365999.1(SZT2):c.9426G>A (p.Val3142=) rs1328052292
NM_001365999.1(SZT2):c.9576C>T (p.Phe3192=)
NM_001365999.1(SZT2):c.9723G>A (p.Ala3241=) rs146635122
NM_001365999.1(SZT2):c.9732G>A (p.Pro3244=)
NM_001365999.1(SZT2):c.9828C>T (p.Asp3276=)
NM_001365999.1(SZT2):c.9883C>T (p.Leu3295=)

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