ClinVar Miner

List of variants in gene SZT2 reported by Athena Diagnostics Inc

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Gene type:
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Total variants: 37
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HGVS dbSNP
NM_001365999.1(SZT2):c.1000G>T (p.Gly334Cys) rs918688605
NM_001365999.1(SZT2):c.1336C>T (p.Pro446Ser) rs2782643
NM_001365999.1(SZT2):c.2631C>T (p.Thr877=) rs140831372
NM_001365999.1(SZT2):c.2888A>G (p.Lys963Arg) rs144176855
NM_001365999.1(SZT2):c.2916G>T (p.Pro972=) rs758017419
NM_001365999.1(SZT2):c.2929+9G>A rs114863461
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.368A>G (p.His123Arg) rs147519875
NM_001365999.1(SZT2):c.4051T>C (p.Trp1351Arg) rs72883814
NM_001365999.1(SZT2):c.4187G>A (p.Ser1396Asn) rs1557564323
NM_001365999.1(SZT2):c.4701G>A (p.Leu1567=) rs111932993
NM_001365999.1(SZT2):c.4710G>A (p.Thr1570=) rs375889333
NM_001365999.1(SZT2):c.4898C>T (p.Ser1633Leu) rs138762270
NM_001365999.1(SZT2):c.4983T>C (p.Asp1661=) rs139810154
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.6077C>A (p.Ala2026Glu) rs140427193
NM_001365999.1(SZT2):c.629A>G (p.Gln210Arg) rs1557531808
NM_001365999.1(SZT2):c.6573C>T (p.Asp2191=) rs114046098
NM_001365999.1(SZT2):c.6888C>T (p.Cys2296=) rs72671125
NM_001365999.1(SZT2):c.6977G>A (p.Arg2326Gln) rs146140125
NM_001365999.1(SZT2):c.7149C>T (p.Ala2383=) rs60480887
NM_001365999.1(SZT2):c.7245C>T (p.Ser2415=) rs142822908
NM_001365999.1(SZT2):c.7356A>G (p.Glu2452=) rs2027130
NM_001365999.1(SZT2):c.7513C>T (p.Arg2505Cys) rs199830565
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.7692_7694del (p.Val2565del) rs1557591600
NM_001365999.1(SZT2):c.7718G>C (p.Ser2573Thr) rs755325371
NM_001365999.1(SZT2):c.7743-4A>G rs368440874
NM_001365999.1(SZT2):c.8216C>T (p.Pro2739Leu) rs774032264
NM_001365999.1(SZT2):c.8330G>C (p.Ser2777Thr) rs1570720687
NM_001365999.1(SZT2):c.8626-3T>C rs2255632
NM_001365999.1(SZT2):c.8910C>T (p.Ser2970=) rs116536134
NM_001365999.1(SZT2):c.9439A>G (p.Ser3147Gly) rs754468503

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