ClinVar Miner

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

Included ClinVar conditions (908):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 67
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HGVS dbSNP gnomAD frequency
NM_147686.4(TRAF3IP2):c.1058G>A (p.Gly353Asp) rs148619849 0.00031
NM_147686.4(TRAF3IP2):c.109C>T (p.Pro37Ser) rs748095541 0.00010
NM_147686.4(TRAF3IP2):c.1345C>T (p.Arg449Cys) rs200246882 0.00010
NM_147686.4(TRAF3IP2):c.1435G>A (p.Glu479Lys) rs149504543 0.00009
NM_147686.4(TRAF3IP2):c.1378G>A (p.Val460Ile) rs775776262 0.00005
NM_147686.4(TRAF3IP2):c.167C>T (p.Ser56Phe) rs368757476 0.00003
NM_147686.4(TRAF3IP2):c.1440T>G (p.Asp480Glu) rs141459820 0.00002
NM_147686.4(TRAF3IP2):c.154A>G (p.Met52Val) rs779302845 0.00002
NM_147686.4(TRAF3IP2):c.172G>A (p.Gly58Arg) rs201280730 0.00002
NM_147686.4(TRAF3IP2):c.1063C>G (p.Pro355Ala) rs760916707 0.00001
NM_147686.4(TRAF3IP2):c.107C>T (p.Ala36Val) rs769663442 0.00001
NM_147686.4(TRAF3IP2):c.1082G>A (p.Cys361Tyr) rs773316350 0.00001
NM_147686.4(TRAF3IP2):c.1193A>C (p.Glu398Ala) rs764227946 0.00001
NM_147686.4(TRAF3IP2):c.1328T>C (p.Ile443Thr) rs1197932494 0.00001
NM_147686.4(TRAF3IP2):c.1408G>A (p.Val470Met) rs1237812708 0.00001
NM_147686.4(TRAF3IP2):c.1457C>T (p.Thr486Ile) rs1419847496 0.00001
NM_147686.4(TRAF3IP2):c.1472G>A (p.Arg491Gln) rs764736740 0.00001
NM_147686.4(TRAF3IP2):c.1507A>G (p.Met503Val) rs1053340006 0.00001
NM_147686.4(TRAF3IP2):c.54G>T (p.Gln18His) rs901070290 0.00001
NM_147686.4(TRAF3IP2):c.868A>G (p.Ile290Val) rs773319517 0.00001
NM_147686.4(TRAF3IP2):c.869T>G (p.Ile290Ser) rs200074354 0.00001
NM_147686.4(TRAF3IP2):c.878C>G (p.Ala293Gly) rs1262799162 0.00001
NM_147686.4(TRAF3IP2):c.982G>A (p.Ala328Thr) rs751906100 0.00001
NC_000006.11:g.(?_111901380)_(111913289_?)dup
NC_000006.12:g.(?_111559385)_(111592106_?)dup
NM_147686.4(TRAF3IP2):c.1004C>T (p.Pro335Leu)
NM_147686.4(TRAF3IP2):c.1006G>C (p.Gly336Arg)
NM_147686.4(TRAF3IP2):c.1021C>G (p.Gln341Glu) rs1239436121
NM_147686.4(TRAF3IP2):c.1022+3A>G rs1562427078
NM_147686.4(TRAF3IP2):c.1023-3T>C rs2128375807
NM_147686.4(TRAF3IP2):c.1049A>G (p.Asn350Ser) rs2128375781
NM_147686.4(TRAF3IP2):c.1058G>C (p.Gly353Ala) rs148619849
NM_147686.4(TRAF3IP2):c.1064C>T (p.Pro355Leu)
NM_147686.4(TRAF3IP2):c.1121C>A (p.Ser374Tyr) rs1795962978
NM_147686.4(TRAF3IP2):c.1126G>A (p.Ala376Thr) rs2128375712
NM_147686.4(TRAF3IP2):c.1201C>T (p.Arg401Trp) rs767596361
NM_147686.4(TRAF3IP2):c.1249A>G (p.Lys417Glu) rs1253864619
NM_147686.4(TRAF3IP2):c.124A>G (p.Met42Val)
NM_147686.4(TRAF3IP2):c.133A>G (p.Asn45Asp)
NM_147686.4(TRAF3IP2):c.1345C>A (p.Arg449Ser)
NM_147686.4(TRAF3IP2):c.1346G>A (p.Arg449His)
NM_147686.4(TRAF3IP2):c.135C>G (p.Asn45Lys)
NM_147686.4(TRAF3IP2):c.1360-9C>G rs1795644367
NM_147686.4(TRAF3IP2):c.1370T>C (p.Met457Thr)
NM_147686.4(TRAF3IP2):c.1396T>A (p.Tyr466Asn) rs1795641126
NM_147686.4(TRAF3IP2):c.1417G>A (p.Ala473Thr) rs111815306
NM_147686.4(TRAF3IP2):c.1477-13T>A
NM_147686.4(TRAF3IP2):c.152C>T (p.Thr51Ile)
NM_147686.4(TRAF3IP2):c.1552G>T (p.Glu518Ter) rs1562415808
NM_147686.4(TRAF3IP2):c.1564A>G (p.Thr522Ala) rs2128368098
NM_147686.4(TRAF3IP2):c.1574A>G (p.Gln525Arg) rs2128368087
NM_147686.4(TRAF3IP2):c.1597C>T (p.Pro533Ser)
NM_147686.4(TRAF3IP2):c.1613dup (p.Asn538fs) rs777439425
NM_147686.4(TRAF3IP2):c.1636G>A (p.Glu546Lys)
NM_147686.4(TRAF3IP2):c.1681C>T (p.Gln561Ter) rs1562415669
NM_147686.4(TRAF3IP2):c.169T>C (p.Ser57Pro)
NM_147686.4(TRAF3IP2):c.16C>G (p.Pro6Ala) rs1471659672
NM_147686.4(TRAF3IP2):c.43T>G (p.Tyr15Asp)
NM_147686.4(TRAF3IP2):c.6C>A (p.Asn2Lys) rs1796544834
NM_147686.4(TRAF3IP2):c.83C>T (p.Pro28Leu) rs369345925
NM_147686.4(TRAF3IP2):c.854C>A (p.Ala285Asp)
NM_147686.4(TRAF3IP2):c.874C>A (p.Pro292Thr) rs1402886359
NM_147686.4(TRAF3IP2):c.88G>A (p.Glu30Lys) rs762683742
NM_147686.4(TRAF3IP2):c.893C>A (p.Pro298His)
NM_147686.4(TRAF3IP2):c.934_936del (p.Lys312del)
NM_147686.4(TRAF3IP2):c.959C>T (p.Pro320Leu)
NM_147686.4(TRAF3IP2):c.989G>C (p.Arg330Thr)

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