ClinVar Miner

List of variants in gene SZT2 reported as uncertain significance for not specified

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Total variants: 33
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HGVS dbSNP
NM_001365999.1(SZT2):c.1272A>G (p.Gln424=) rs780157180
NM_001365999.1(SZT2):c.2138G>T (p.Gly713Val) rs766656735
NM_001365999.1(SZT2):c.2477G>A (p.Arg826Gln) rs752495437
NM_001365999.1(SZT2):c.3511G>T (p.Gly1171Trp) rs201767217
NM_001365999.1(SZT2):c.4069C>A (p.Pro1357Thr) rs748826670
NM_001365999.1(SZT2):c.4225C>T (p.Pro1409Ser) rs377512674
NM_001365999.1(SZT2):c.4342C>T (p.Arg1448Cys) rs140004653
NM_001365999.1(SZT2):c.4457A>C (p.Glu1486Ala) rs1060503546
NM_001365999.1(SZT2):c.4503G>A (p.Val1501=) rs367690658
NM_001365999.1(SZT2):c.4647C>T (p.Gly1549=) rs149192929
NM_001365999.1(SZT2):c.4721G>A (p.Arg1574Gln) rs532357677
NM_001365999.1(SZT2):c.4727G>A (p.Arg1576His) rs143935839
NM_001365999.1(SZT2):c.4892C>T (p.Thr1631Met) rs201312287
NM_001365999.1(SZT2):c.5167G>A (p.Ala1723Thr) rs774902064
NM_001365999.1(SZT2):c.5316A>G (p.Glu1772=) rs797046032
NM_001365999.1(SZT2):c.5345C>T (p.Ala1782Val) rs138028425
NM_001365999.1(SZT2):c.5377G>A (p.Glu1793Lys) rs143185010
NM_001365999.1(SZT2):c.5645A>G (p.Asn1882Ser) rs573213368
NM_001365999.1(SZT2):c.5665G>T (p.Ala1889Ser) rs370230435
NM_001365999.1(SZT2):c.5772G>T (p.Leu1924=) rs187188981
NM_001365999.1(SZT2):c.5780G>T (p.Arg1927Leu) rs375009349
NM_001365999.1(SZT2):c.6290+3A>T rs878855009
NM_001365999.1(SZT2):c.6380A>T (p.Tyr2127Phe) rs149812437
NM_001365999.1(SZT2):c.7012C>G (p.Arg2338Gly) rs752242169
NM_001365999.1(SZT2):c.7613G>A (p.Cys2538Tyr) rs1553153691
NM_001365999.1(SZT2):c.8039G>A (p.Arg2680His) rs144218947
NM_001365999.1(SZT2):c.8177C>G (p.Thr2726Ser) rs145882968
NM_001365999.1(SZT2):c.8182G>C (p.Glu2728Gln) rs1553154186
NM_001365999.1(SZT2):c.8201G>A (p.Arg2734Gln) rs370164213
NM_001365999.1(SZT2):c.8479C>T (p.Pro2827Ser) rs762098815
NM_001365999.1(SZT2):c.8594C>T (p.Pro2865Leu) rs374031590
NM_001365999.1(SZT2):c.8916+8G>A rs147419780
NM_001365999.1(SZT2):c.92G>A (p.Arg31His) rs772662249

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