ClinVar Miner

List of variants in gene TRAF3IP2 reported as likely benign for immune system disorder

Included ClinVar conditions (908):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 56
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HGVS dbSNP gnomAD frequency
NM_147686.4(TRAF3IP2):c.1184A>G (p.Asn395Ser) rs139767840 0.00174
NM_147686.4(TRAF3IP2):c.1119G>A (p.Pro373=) rs370011231 0.00027
NM_147686.4(TRAF3IP2):c.8G>A (p.Arg3Gln) rs148778036 0.00015
NM_147686.4(TRAF3IP2):c.1089A>G (p.Ala363=) rs904037371 0.00012
NM_147686.4(TRAF3IP2):c.1552-6C>A rs202020640 0.00009
NM_147686.4(TRAF3IP2):c.1377C>T (p.Ile459=) rs371382152 0.00008
NM_147686.4(TRAF3IP2):c.171C>T (p.Ser57=) rs144366791 0.00006
NM_147686.4(TRAF3IP2):c.1290+15C>T rs778369631 0.00005
NM_147686.4(TRAF3IP2):c.1185T>C (p.Asn395=) rs753954583 0.00004
NM_147686.4(TRAF3IP2):c.1551+14G>C rs201855498 0.00004
NM_147686.4(TRAF3IP2):c.981C>T (p.Pro327=) rs112036127 0.00004
NM_147686.4(TRAF3IP2):c.1275T>C (p.Asn425=) rs571096374 0.00003
NM_147686.4(TRAF3IP2):c.1674C>A (p.Pro558=) rs769958417 0.00003
NM_147686.4(TRAF3IP2):c.1022+7A>G rs759269153 0.00002
NM_147686.4(TRAF3IP2):c.830-14G>A rs753149212 0.00002
NM_147686.4(TRAF3IP2):c.1008G>A (p.Gly336=) rs761822683 0.00001
NM_147686.4(TRAF3IP2):c.1023-4C>G rs1795968896 0.00001
NM_147686.4(TRAF3IP2):c.1224G>A (p.Ser408=) rs761644425 0.00001
NM_147686.4(TRAF3IP2):c.1266G>A (p.Leu422=) rs894860257 0.00001
NM_147686.4(TRAF3IP2):c.1344G>A (p.Glu448=) rs200991285 0.00001
NM_147686.4(TRAF3IP2):c.1524C>T (p.Ile508=) rs905169151 0.00001
NM_147686.4(TRAF3IP2):c.1692C>G (p.Pro564=) rs143248990 0.00001
NM_147686.4(TRAF3IP2):c.936G>A (p.Lys312=) rs1221925762 0.00001
NM_147686.4(TRAF3IP2):c.993C>T (p.Asp331=) rs562058180 0.00001
NM_147686.4(TRAF3IP2):c.1022+16C>A
NM_147686.4(TRAF3IP2):c.1032A>G (p.Pro344=)
NM_147686.4(TRAF3IP2):c.1071G>A (p.Glu357=)
NM_147686.4(TRAF3IP2):c.1201+12G>C rs1388493620
NM_147686.4(TRAF3IP2):c.1202-16A>G rs2128374377
NM_147686.4(TRAF3IP2):c.1236T>C (p.Ala412=)
NM_147686.4(TRAF3IP2):c.1254C>T (p.Phe418=)
NM_147686.4(TRAF3IP2):c.1291-14C>G rs2128372070
NM_147686.4(TRAF3IP2):c.1291-8T>G rs2128372058
NM_147686.4(TRAF3IP2):c.1360-13C>G rs2128371456
NM_147686.4(TRAF3IP2):c.1360-15C>G
NM_147686.4(TRAF3IP2):c.1407C>T (p.Asp469=)
NM_147686.4(TRAF3IP2):c.1416C>T (p.Gly472=)
NM_147686.4(TRAF3IP2):c.1434C>T (p.Asp478=)
NM_147686.4(TRAF3IP2):c.144T>G (p.Ser48=)
NM_147686.4(TRAF3IP2):c.1477-15T>C
NM_147686.4(TRAF3IP2):c.1530G>A (p.Val510=)
NM_147686.4(TRAF3IP2):c.1551+10_1551+13del rs749643257
NM_147686.4(TRAF3IP2):c.1551+14_1551+17del rs576438307
NM_147686.4(TRAF3IP2):c.1551+17del rs1477878905
NM_147686.4(TRAF3IP2):c.1575G>A (p.Gln525=) rs2128368085
NM_147686.4(TRAF3IP2):c.1677C>G (p.Thr559=)
NM_147686.4(TRAF3IP2):c.1680T>C (p.Leu560=)
NM_147686.4(TRAF3IP2):c.1686G>T (p.Val562=)
NM_147686.4(TRAF3IP2):c.72A>G (p.Pro24=)
NM_147686.4(TRAF3IP2):c.830-7C>T
NM_147686.4(TRAF3IP2):c.83C>G (p.Pro28Arg) rs369345925
NM_147686.4(TRAF3IP2):c.840C>T (p.Asp280=)
NM_147686.4(TRAF3IP2):c.876G>A (p.Pro292=)
NM_147686.4(TRAF3IP2):c.906C>T (p.Ala302=) rs2128377807
NM_147686.4(TRAF3IP2):c.969C>T (p.His323=)
NM_147686.4(TRAF3IP2):c.984A>G (p.Ala328=)

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