ClinVar Miner

List of variants in gene TRIM2 reported as uncertain significance for Charcot-Marie-Tooth disease

Included ClinVar conditions (137):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 76
Download table as spreadsheet
HGVS dbSNP
NM_015271.5(TRIM2):c.1028G>C (p.Gly343Ala)
NM_015271.5(TRIM2):c.1043C>G (p.Thr348Ser) rs752113810
NM_015271.5(TRIM2):c.1073C>T (p.Thr358Met) rs756377335
NM_015271.5(TRIM2):c.1083G>T (p.Gly361=) rs779795369
NM_015271.5(TRIM2):c.1087C>T (p.Arg363Trp) rs768541205
NM_015271.5(TRIM2):c.1093A>C (p.Thr365Pro)
NM_015271.5(TRIM2):c.1094C>G (p.Thr365Ser) rs146686472
NM_015271.5(TRIM2):c.1144G>T (p.Gly382Cys) rs760086023
NM_015271.5(TRIM2):c.1166A>G (p.Asn389Ser)
NM_015271.5(TRIM2):c.1180G>A (p.Ala394Thr)
NM_015271.5(TRIM2):c.121C>T (p.Arg41Cys)
NM_015271.5(TRIM2):c.1232A>G (p.Asn411Ser)
NM_015271.5(TRIM2):c.1243A>G (p.Thr415Ala)
NM_015271.5(TRIM2):c.1319G>A (p.Arg440Gln)
NM_015271.5(TRIM2):c.1330T>C (p.Phe444Leu) rs1579436975
NM_015271.5(TRIM2):c.1349G>A (p.Arg450Gln) rs777541972
NM_015271.5(TRIM2):c.1381G>C (p.Val461Leu) rs147859999
NM_015271.5(TRIM2):c.1411G>A (p.Gly471Ser)
NM_015271.5(TRIM2):c.1445C>G (p.Ala482Gly)
NM_015271.5(TRIM2):c.1451T>A (p.Met484Lys)
NM_015271.5(TRIM2):c.1615A>T (p.Ile539Leu)
NM_015271.5(TRIM2):c.1625A>G (p.Asn542Ser) rs374300347
NM_015271.5(TRIM2):c.1646G>A (p.Arg549His) rs1579646798
NM_015271.5(TRIM2):c.1664G>A (p.Arg555His) rs755651013
NM_015271.5(TRIM2):c.1670C>T (p.Pro557Leu)
NM_015271.5(TRIM2):c.1671G>A (p.Pro557=) rs150231451
NM_015271.5(TRIM2):c.1673G>A (p.Gly558Glu) rs1305793582
NM_015271.5(TRIM2):c.167G>A (p.Arg56Gln) rs1418080739
NM_015271.5(TRIM2):c.1746A>G (p.Lys582=)
NM_015271.5(TRIM2):c.1793G>T (p.Gly598Val) rs780090814
NM_015271.5(TRIM2):c.1834C>T (p.Arg612Cys)
NM_015271.5(TRIM2):c.1835G>A (p.Arg612His) rs114415780
NM_015271.5(TRIM2):c.1838A>G (p.Asn613Ser) rs1579720652
NM_015271.5(TRIM2):c.1846A>G (p.Ile616Val) rs1561013892
NM_015271.5(TRIM2):c.1876G>A (p.Val626Met) rs759524701
NM_015271.5(TRIM2):c.1964C>A (p.Ala655Glu) rs1554002777
NM_015271.5(TRIM2):c.1990A>G (p.Ile664Val) rs140853898
NM_015271.5(TRIM2):c.2049G>A (p.Met683Ile) rs1579783522
NM_015271.5(TRIM2):c.210C>T (p.Cys70=) rs750120043
NM_015271.5(TRIM2):c.2197A>G (p.Ile733Val) rs201921014
NM_015271.5(TRIM2):c.2215C>T (p.Pro739Ser) rs199912457
NM_015271.5(TRIM2):c.2220C>G (p.Leu740=) rs763024851
NM_015271.5(TRIM2):c.2265G>A (p.Val755=)
NM_015271.5(TRIM2):c.251C>T (p.Thr84Ile) rs745985238
NM_015271.5(TRIM2):c.305C>T (p.Ala102Val) rs1579254686
NM_015271.5(TRIM2):c.320A>G (p.Asn107Ser)
NM_015271.5(TRIM2):c.328A>G (p.Ile110Val) rs1435917917
NM_015271.5(TRIM2):c.346G>A (p.Val116Met) rs763365056
NM_015271.5(TRIM2):c.367A>T (p.Ser123Cys)
NM_015271.5(TRIM2):c.388A>G (p.Ile130Val)
NM_015271.5(TRIM2):c.415G>C (p.Ala139Pro)
NM_015271.5(TRIM2):c.417G>A (p.Ala139=)
NM_015271.5(TRIM2):c.461A>G (p.Glu154Gly)
NM_015271.5(TRIM2):c.485C>A (p.Thr162Asn) rs1579407719
NM_015271.5(TRIM2):c.497G>A (p.Arg166Gln) rs146252965
NM_015271.5(TRIM2):c.512G>C (p.Gly171Ala) rs1553992552
NM_015271.5(TRIM2):c.520G>A (p.Ala174Thr) rs200706275
NM_015271.5(TRIM2):c.520G>T (p.Ala174Ser)
NM_015271.5(TRIM2):c.541C>T (p.Leu181Phe) rs754986666
NM_015271.5(TRIM2):c.550G>A (p.Val184Met) rs1579408437
NM_015271.5(TRIM2):c.560A>G (p.Gln187Arg) rs1579408472
NM_015271.5(TRIM2):c.561G>T (p.Gln187His)
NM_015271.5(TRIM2):c.568G>A (p.Ala190Thr)
NM_015271.5(TRIM2):c.605+6G>A
NM_015271.5(TRIM2):c.653A>G (p.His218Arg)
NM_015271.5(TRIM2):c.659T>C (p.Leu220Ser) rs759938444
NM_015271.5(TRIM2):c.673G>T (p.Ala225Ser)
NM_015271.5(TRIM2):c.677G>A (p.Ser226Asn) rs143032564
NM_015271.5(TRIM2):c.688G>T (p.Asp230Tyr) rs1560963959
NM_015271.5(TRIM2):c.756A>C (p.Glu252Asp) rs138228404
NM_015271.5(TRIM2):c.822G>T (p.Gly274=)
NM_015271.5(TRIM2):c.830G>A (p.Ser277Asn)
NM_015271.5(TRIM2):c.914G>A (p.Ser305Asn) rs1579432032
NM_015271.5(TRIM2):c.916G>C (p.Glu306Gln) rs750001904
NM_015271.5(TRIM2):c.928G>A (p.Glu310Lys)
NM_015271.5(TRIM2):c.959C>T (p.Pro320Leu) rs1279083060

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.