ClinVar Miner

List of variants in gene SZT2 reported as benign by Invitae

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Gene type:
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Total variants: 32
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HGVS dbSNP
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.2929+9G>A rs114863461
NM_001365999.1(SZT2):c.3267C>T (p.Val1089=) rs147008168
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.3570C>T (p.Val1190=) rs147644619
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.4531G>A (p.Val1511Ile) rs76675748
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.5198G>A (p.Arg1733His) rs147797700
NM_001365999.1(SZT2):c.5385T>G (p.Ser1795=) rs12129487
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.6543A>G (p.Leu2181=) rs112461557
NM_001365999.1(SZT2):c.6888C>T (p.Cys2296=) rs72671125
NM_001365999.1(SZT2):c.7245C>T (p.Ser2415=) rs142822908
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.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.7975-10C>T rs181831231
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.8910C>T (p.Ser2970=) rs116536134
NM_001365999.1(SZT2):c.9723G>A (p.Ala3241=) rs146635122

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