ClinVar Miner

List of variants in gene TNFAIP3 reported as uncertain significance for autoinflammatory syndrome

Included ClinVar conditions (114):
Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 27
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HGVS dbSNP gnomAD frequency
NM_001270508.2(TNFAIP3):c.374C>T (p.Ala125Val) rs5029941 0.00569
NM_001270508.2(TNFAIP3):c.1939A>C (p.Thr647Pro) rs142253225 0.00189
NM_001270508.2(TNFAIP3):c.1634C>T (p.Ala545Val) rs142752989 0.00067
NM_001270508.2(TNFAIP3):c.2231G>A (p.Gly744Asp) rs150355046 0.00043
NM_001270508.2(TNFAIP3):c.2090G>A (p.Arg697Lys) rs201429571 0.00034
NM_001270508.2(TNFAIP3):c.1193T>C (p.Val398Ala) rs140616865 0.00018
NM_001270508.2(TNFAIP3):c.839G>A (p.Arg280Gln) rs200840068 0.00012
NM_001270508.2(TNFAIP3):c.1182C>A (p.Phe394Leu) rs762710607 0.00004
NM_001270508.2(TNFAIP3):c.1757C>T (p.Ala586Val) rs756832433 0.00002
NM_001270508.2(TNFAIP3):c.929T>C (p.Ile310Thr) rs530310566 0.00002
NM_001270508.2(TNFAIP3):c.1294G>A (p.Gly432Ser) rs1453719653 0.00001
NM_001270508.2(TNFAIP3):c.1306G>A (p.Gly436Arg) rs766691413 0.00001
NM_001270508.2(TNFAIP3):c.1828G>A (p.Ala610Thr) rs1776363649 0.00001
NM_001270508.2(TNFAIP3):c.1102C>T (p.His368Tyr)
NM_001270508.2(TNFAIP3):c.113A>G (p.His38Arg)
NM_001270508.2(TNFAIP3):c.1474A>C (p.Asn492His)
NM_001270508.2(TNFAIP3):c.1555G>A (p.Gly519Arg) rs762149390
NM_001270508.2(TNFAIP3):c.1809G>T (p.Gly603=) rs201052251
NM_001270508.2(TNFAIP3):c.181C>T (p.Arg61Trp)
NM_001270508.2(TNFAIP3):c.1993C>G (p.Leu665Val)
NM_001270508.2(TNFAIP3):c.2137A>G (p.Arg713Gly)
NM_001270508.2(TNFAIP3):c.2149G>A (p.Ala717Thr)
NM_001270508.2(TNFAIP3):c.227C>T (p.Thr76Ile) rs1776060477
NM_001270508.2(TNFAIP3):c.260G>A (p.Arg87Gln)
NM_001270508.2(TNFAIP3):c.872T>G (p.Leu291Trp)
NM_001270508.2(TNFAIP3):c.881C>T (p.Pro294Leu) rs756723486
NM_001270508.2(TNFAIP3):c.980C>T (p.Ala327Val) rs1210641937

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