ClinVar Miner

List of variants in gene TNFAIP3 reported as not provided

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 19
Download table as spreadsheet
HGVS dbSNP
NM_001270508.2(TNFAIP3):c.1634C>T (p.Ala545Val) rs142752989
NM_001270508.2(TNFAIP3):c.1939A>C (p.Thr647Pro) rs142253225
NM_001270508.2(TNFAIP3):c.2036T>C (p.Ile679Thr) rs140610274
NM_001270508.2(TNFAIP3):c.2231G>A (p.Gly744Asp) rs150355046
NM_001270508.2(TNFAIP3):c.305A>G (p.Asn102Ser) rs146534657
NM_001270508.2(TNFAIP3):c.322A>G (p.Thr108Ala) rs376205580
NM_001270508.2(TNFAIP3):c.374C>T (p.Ala125Val) rs5029941
NM_001270508.2(TNFAIP3):c.380T>G (p.Phe127Cys) rs2230926
NM_001270508.2(TNFAIP3):c.619A>C (p.Ile207Leu) rs141807543
NM_001270508.2(TNFAIP3):c.742A>G (p.Ile248Val) rs587778711
NM_001270508.2(TNFAIP3):c.839G>A (p.Arg280Gln) rs200840068
NM_006290.4(TNFAIP3):c.1208T>C (p.Leu403Ser) rs587778715
NM_006290.4(TNFAIP3):c.1232G>A (p.Arg411Gln) rs587778713
NM_006290.4(TNFAIP3):c.1364G>A (p.Gly455Glu) rs587778714
NM_006290.4(TNFAIP3):c.1651C>T (p.Leu551Phe) rs587778712
NM_006290.4(TNFAIP3):c.1771C>G (p.Leu591Val) rs145392420
NM_006290.4(TNFAIP3):c.1811C>G (p.Thr604Arg) rs564646155
NM_006290.4(TNFAIP3):c.2140C>G (p.Pro714Ala) rs369155845
NM_006290.4(TNFAIP3):c.484C>T (p.Arg162Trp) rs587778710

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.