ClinVar Miner

List of variants in gene STAG2 reported as uncertain significance by GeneDx

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Gene type:
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Total variants: 74
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HGVS dbSNP gnomAD frequency
NM_001042750.2(STAG2):c.862A>G (p.Ile288Val) rs745329478 0.00006
NM_001042750.2(STAG2):c.2314T>A (p.Cys772Ser) rs762388218 0.00003
NM_001042750.2(STAG2):c.2924+5T>A rs1230977778 0.00003
NM_001042750.2(STAG2):c.2176C>T (p.Pro726Ser) rs138155911 0.00002
NM_001042750.2(STAG2):c.1298A>G (p.Tyr433Cys) rs764885530 0.00001
NM_001042750.2(STAG2):c.1999C>T (p.Arg667Trp) rs776905490 0.00001
NM_001042750.2(STAG2):c.3016T>C (p.Phe1006Leu) rs987552896 0.00001
NM_001042750.2(STAG2):c.3584G>A (p.Arg1195His) rs1430304708 0.00001
NM_001042750.2(STAG2):c.386-12T>G rs1293835583 0.00001
NM_001042750.2(STAG2):c.-97-3A>G rs2523544751
NM_001042750.2(STAG2):c.1024G>A (p.Glu342Lys)
NM_001042750.2(STAG2):c.1151A>T (p.Tyr384Phe)
NM_001042750.2(STAG2):c.1237G>T (p.Val413Phe) rs2521586906
NM_001042750.2(STAG2):c.1241A>T (p.Tyr414Phe)
NM_001042750.2(STAG2):c.1264C>T (p.Arg422Trp) rs2058189918
NM_001042750.2(STAG2):c.1283C>G (p.Ala428Gly)
NM_001042750.2(STAG2):c.1315C>T (p.Arg439Cys) rs2058254106
NM_001042750.2(STAG2):c.1394T>C (p.Val465Ala)
NM_001042750.2(STAG2):c.1415A>G (p.Glu472Gly)
NM_001042750.2(STAG2):c.1570A>G (p.Ile524Val) rs144820719
NM_001042750.2(STAG2):c.1595C>T (p.Ala532Val) rs2148312064
NM_001042750.2(STAG2):c.1651A>G (p.Lys551Glu) rs2148319624
NM_001042750.2(STAG2):c.166G>A (p.Gly56Ser) rs761786663
NM_001042750.2(STAG2):c.1678A>G (p.Arg560Gly)
NM_001042750.2(STAG2):c.1720T>G (p.Leu574Val)
NM_001042750.2(STAG2):c.1822-16TAT[2] rs1356736514
NM_001042750.2(STAG2):c.1923T>A (p.Asn641Lys) rs1447770328
NM_001042750.2(STAG2):c.1933A>G (p.Thr645Ala) rs747288424
NM_001042750.2(STAG2):c.1960A>G (p.Arg654Gly) rs2521834723
NM_001042750.2(STAG2):c.2026-8dup
NM_001042750.2(STAG2):c.2075A>G (p.Lys692Arg)
NM_001042750.2(STAG2):c.2171A>G (p.Asp724Gly)
NM_001042750.2(STAG2):c.2175G>A (p.Met725Ile) rs2148343231
NM_001042750.2(STAG2):c.2176C>A (p.Pro726Thr) rs138155911
NM_001042750.2(STAG2):c.2206T>C (p.Cys736Arg) rs2521911073
NM_001042750.2(STAG2):c.2207G>C (p.Cys736Ser)
NM_001042750.2(STAG2):c.2222T>A (p.Ile741Asn)
NM_001042750.2(STAG2):c.2227T>A (p.Trp743Arg) rs2148344352
NM_001042750.2(STAG2):c.2278C>T (p.Arg760Cys) rs2058595620
NM_001042750.2(STAG2):c.2294T>C (p.Met765Thr)
NM_001042750.2(STAG2):c.2309A>G (p.Gln770Arg) rs2148357605
NM_001042750.2(STAG2):c.2332A>G (p.Asn778Asp)
NM_001042750.2(STAG2):c.2495A>G (p.His832Arg)
NM_001042750.2(STAG2):c.2504T>C (p.Ile835Thr)
NM_001042750.2(STAG2):c.2518G>A (p.Asp840Asn) rs2058657386
NM_001042750.2(STAG2):c.2536G>A (p.Gly846Ser) rs1208998954
NM_001042750.2(STAG2):c.2537G>T (p.Gly846Val) rs2148406190
NM_001042750.2(STAG2):c.2575C>T (p.His859Tyr)
NM_001042750.2(STAG2):c.2623A>C (p.Thr875Pro)
NM_001042750.2(STAG2):c.2674-13A>G rs1392293594
NM_001042750.2(STAG2):c.2771A>G (p.Gln924Arg) rs2522195750
NM_001042750.2(STAG2):c.2783A>T (p.Asn928Ile)
NM_001042750.2(STAG2):c.2803G>T (p.Gly935Cys)
NM_001042750.2(STAG2):c.2837G>T (p.Ser946Ile) rs2148434622
NM_001042750.2(STAG2):c.284T>C (p.Met95Thr) rs2148062729
NM_001042750.2(STAG2):c.2897C>G (p.Thr966Arg) rs1603150691
NM_001042750.2(STAG2):c.2930G>A (p.Gly977Asp)
NM_001042750.2(STAG2):c.295G>A (p.Val99Ile)
NM_001042750.2(STAG2):c.316T>A (p.Tyr106Asn)
NM_001042750.2(STAG2):c.3211C>T (p.Arg1071Trp) rs2059116377
NM_001042750.2(STAG2):c.3232T>G (p.Ser1078Ala) rs373076855
NM_001042750.2(STAG2):c.329G>A (p.Arg110Gln)
NM_001042750.2(STAG2):c.3306G>A (p.Met1102Ile)
NM_001042750.2(STAG2):c.3415A>G (p.Met1139Val)
NM_001042750.2(STAG2):c.3533C>G (p.Ala1178Gly)
NM_001042750.2(STAG2):c.3613G>A (p.Glu1205Lys) rs927258952
NM_001042750.2(STAG2):c.3665T>C (p.Leu1222Pro) rs2148504213
NM_001042750.2(STAG2):c.457G>A (p.Asp153Asn)
NM_001042750.2(STAG2):c.461A>G (p.Glu154Gly) rs2148158754
NM_001042750.2(STAG2):c.551G>A (p.Arg184Gln) rs1239781217
NM_001042750.2(STAG2):c.721A>G (p.Met241Val)
NM_001042750.2(STAG2):c.797_798delinsAA (p.Leu266Gln) rs2148196105
NM_001042750.2(STAG2):c.826G>A (p.Glu276Lys)
NM_001042750.2(STAG2):c.893+5G>T rs2148209871

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