ClinVar Miner

List of variants in gene combination LOC114803478, TRAF3IP2 reported as uncertain significance for immune system disorder

Included ClinVar conditions (908):
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Total variants: 54
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HGVS dbSNP gnomAD frequency
NM_147686.4(TRAF3IP2):c.232C>G (p.Arg78Gly) rs73764462 0.00229
NM_147686.4(TRAF3IP2):c.819C>G (p.His273Gln) rs144405088 0.00172
NM_147686.4(TRAF3IP2):c.641G>A (p.Arg214Lys) rs181942095 0.00020
NM_147686.4(TRAF3IP2):c.566G>A (p.Gly189Asp) rs138401155 0.00014
NM_147686.4(TRAF3IP2):c.691C>T (p.Leu231Phe) rs149860754 0.00010
NM_147686.4(TRAF3IP2):c.758C>G (p.Pro253Arg) rs146627823 0.00010
NM_147686.4(TRAF3IP2):c.497C>T (p.Ala166Val) rs371756748 0.00008
NM_147686.4(TRAF3IP2):c.704A>C (p.Glu235Ala) rs771255680 0.00006
NM_147686.4(TRAF3IP2):c.343G>A (p.Glu115Lys) rs747398904 0.00004
NM_147686.4(TRAF3IP2):c.560G>A (p.Arg187Gln) rs769293100 0.00004
NM_147686.4(TRAF3IP2):c.822G>C (p.Gln274His) rs535612529 0.00004
NM_147686.4(TRAF3IP2):c.625A>C (p.Ile209Leu) rs997754649 0.00003
NM_147686.4(TRAF3IP2):c.233G>A (p.Arg78Gln) rs973361796 0.00002
NM_147686.4(TRAF3IP2):c.661G>A (p.Val221Met) rs145697646 0.00002
NM_147686.4(TRAF3IP2):c.749T>A (p.Met250Lys) rs754775237 0.00002
NM_147686.4(TRAF3IP2):c.409C>T (p.Arg137Cys) rs755092394 0.00001
NM_147686.4(TRAF3IP2):c.410G>A (p.Arg137His) rs1243216801 0.00001
NM_147686.4(TRAF3IP2):c.454A>T (p.Thr152Ser) rs1796521013 0.00001
NM_147686.4(TRAF3IP2):c.515G>A (p.Gly172Asp) rs755391775 0.00001
NM_147686.4(TRAF3IP2):c.542C>T (p.Pro181Leu) rs376991338 0.00001
NM_147686.4(TRAF3IP2):c.580A>G (p.Thr194Ala) rs147059564 0.00001
NM_147686.4(TRAF3IP2):c.701G>C (p.Arg234Thr) rs774269212 0.00001
NM_147686.4(TRAF3IP2):c.736G>A (p.Ala246Thr) rs1364602237 0.00001
NM_147686.4(TRAF3IP2):c.761A>G (p.Asn254Ser) rs1463029619 0.00001
NM_147686.4(TRAF3IP2):c.764T>C (p.Leu255Pro) rs1002090925 0.00001
NM_147686.4(TRAF3IP2):c.766T>C (p.Ser256Pro) rs779990190 0.00001
NM_147686.4(TRAF3IP2):c.773A>G (p.His258Arg) rs1456391791 0.00001
NM_147686.4(TRAF3IP2):c.221G>A (p.Arg74Gln) rs149247775
NM_147686.4(TRAF3IP2):c.233G>T (p.Arg78Leu) rs973361796
NM_147686.4(TRAF3IP2):c.250C>T (p.Arg84Cys)
NM_147686.4(TRAF3IP2):c.251G>A (p.Arg84His)
NM_147686.4(TRAF3IP2):c.259G>A (p.Val87Ile)
NM_147686.4(TRAF3IP2):c.299C>G (p.Pro100Arg)
NM_147686.4(TRAF3IP2):c.373C>T (p.Leu125Phe) rs1796525340
NM_147686.4(TRAF3IP2):c.377C>A (p.Pro126His)
NM_147686.4(TRAF3IP2):c.385C>T (p.His129Tyr) rs927235073
NM_147686.4(TRAF3IP2):c.440C>T (p.Ala147Val)
NM_147686.4(TRAF3IP2):c.461A>G (p.His154Arg)
NM_147686.4(TRAF3IP2):c.476C>T (p.Ser159Leu) rs372064320
NM_147686.4(TRAF3IP2):c.517G>A (p.Gly173Ser) rs750659136
NM_147686.4(TRAF3IP2):c.518G>A (p.Gly173Asp) rs1796516657
NM_147686.4(TRAF3IP2):c.521G>A (p.Ser174Asn) rs1562433434
NM_147686.4(TRAF3IP2):c.531G>A (p.Met177Ile) rs1325874110
NM_147686.4(TRAF3IP2):c.560_561delinsAT (p.Arg187His) rs2128382170
NM_147686.4(TRAF3IP2):c.563C>T (p.Ala188Val)
NM_147686.4(TRAF3IP2):c.583A>G (p.Ile195Val) rs1796512488
NM_147686.4(TRAF3IP2):c.640A>G (p.Arg214Gly)
NM_147686.4(TRAF3IP2):c.676G>C (p.Asp226His) rs2128382106
NM_147686.4(TRAF3IP2):c.691C>G (p.Leu231Val) rs149860754
NM_147686.4(TRAF3IP2):c.760A>G (p.Asn254Asp) rs1562433144
NM_147686.4(TRAF3IP2):c.767C>G (p.Ser256Cys) rs1562433128
NM_147686.4(TRAF3IP2):c.811C>T (p.Pro271Ser)
NM_147686.4(TRAF3IP2):c.814G>T (p.Asp272Tyr) rs757470698
NM_147686.4(TRAF3IP2):c.826C>A (p.Pro276Thr)

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