ClinVar Miner

List of variants in gene SZT2 reported as likely benign by PreventionGenetics, part of Exact Sciences

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Total variants: 49
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HGVS dbSNP gnomAD frequency
NM_001365999.1(SZT2):c.2631C>T (p.Thr877=) rs140831372 0.00717
NM_001365999.1(SZT2):c.6543A>G (p.Leu2181=) rs112461557 0.00596
NM_001365999.1(SZT2):c.4531G>A (p.Val1511Ile) rs76675748 0.00361
NM_001365999.1(SZT2):c.9782G>A (p.Arg3261Gln) rs190363418 0.00207
NM_001365999.1(SZT2):c.6380A>T (p.Tyr2127Phe) rs149812437 0.00200
NM_001365999.1(SZT2):c.4898C>T (p.Ser1633Leu) rs138762270 0.00197
NM_001365999.1(SZT2):c.7344+9A>G rs184417929 0.00181
NM_001365999.1(SZT2):c.2955C>T (p.Cys985=) rs151189395 0.00113
NM_001365999.1(SZT2):c.8702C>T (p.Pro2901Leu) rs139027171 0.00093
NM_001365999.1(SZT2):c.9576C>T (p.Phe3192=) rs138585463 0.00085
NM_001365999.1(SZT2):c.6343C>G (p.Pro2115Ala) rs147309177 0.00073
NM_001365999.1(SZT2):c.6977G>A (p.Arg2326Gln) rs146140125 0.00068
NM_001365999.1(SZT2):c.7641C>T (p.His2547=) rs144699351 0.00063
NM_001365999.1(SZT2):c.4342C>T (p.Arg1448Cys) rs140004653 0.00061
NM_001365999.1(SZT2):c.9887G>T (p.Gly3296Val) rs368272173 0.00061
NM_001365999.1(SZT2):c.8944C>T (p.His2982Tyr) rs754779853 0.00045
NM_001365999.1(SZT2):c.5937C>T (p.His1979=) rs149717460 0.00038
NM_001365999.1(SZT2):c.8148A>G (p.Glu2716=) rs199826167 0.00023
NM_001365999.1(SZT2):c.1458T>C (p.Arg486=) rs376484331 0.00021
NM_001365999.1(SZT2):c.528T>C (p.Pro176=) rs780340130 0.00021
NM_001365999.1(SZT2):c.328-6C>T rs771488309 0.00016
NM_001365999.1(SZT2):c.9795G>C (p.Leu3265=) rs569613488 0.00015
NM_001365999.1(SZT2):c.2652G>A (p.Ser884=) rs138653257 0.00013
NM_001365999.1(SZT2):c.8255G>A (p.Arg2752His) rs150591561 0.00013
NM_001365999.1(SZT2):c.7671C>T (p.Ile2557=) rs201311847 0.00012
NM_001365999.1(SZT2):c.9630C>T (p.Arg3210=) rs773985024 0.00012
NM_001365999.1(SZT2):c.5772G>T (p.Leu1924=) rs187188981 0.00011
NM_001365999.1(SZT2):c.5910G>C (p.Leu1970=) rs151260299 0.00011
NM_001365999.1(SZT2):c.3251C>T (p.Pro1084Leu) rs373408367 0.00009
NM_001365999.1(SZT2):c.4892C>T (p.Thr1631Met) rs201312287 0.00009
NM_001365999.1(SZT2):c.5665G>T (p.Ala1889Ser) rs370230435 0.00009
NM_001365999.1(SZT2):c.2256-10C>T rs747740233 0.00007
NM_001365999.1(SZT2):c.28-5C>T rs372519036 0.00007
NM_001365999.1(SZT2):c.3306C>T (p.Ser1102=) rs370803181 0.00006
NM_001365999.1(SZT2):c.9938C>T (p.Ala3313Val) rs201695619 0.00006
NM_001365999.1(SZT2):c.2256-4C>G rs373433199 0.00005
NM_001365999.1(SZT2):c.3355C>G (p.Pro1119Ala) rs137956992 0.00004
NM_001365999.1(SZT2):c.9360T>C (p.Ser3120=) rs367855839 0.00004
NM_001365999.1(SZT2):c.1107A>G (p.Leu369=) rs533632273 0.00003
NM_001365999.1(SZT2):c.531C>T (p.Ser177=) rs1056702956 0.00002
NM_001365999.1(SZT2):c.7708G>A (p.Gly2570Arg) rs563782968 0.00002
NM_001365999.1(SZT2):c.3782C>T (p.Ala1261Val) rs200635457 0.00001
NM_001365999.1(SZT2):c.4401+7G>C rs937666303 0.00001
NM_001365999.1(SZT2):c.4590G>A (p.Ser1530=) rs771463235 0.00001
NM_001365999.1(SZT2):c.3044-7C>T
NM_001365999.1(SZT2):c.3058C>T (p.Pro1020Ser)
NM_001365999.1(SZT2):c.5089-10C>G
NM_001365999.1(SZT2):c.7707T>G (p.Ala2569=)
NM_001365999.1(SZT2):c.9867G>A (p.Gly3289=)

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