ClinVar Miner

List of variants in gene TRAF3 reported as likely benign for central nervous system infectious disorder

Included ClinVar conditions (16):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 151
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_145725.3(TRAF3):c.352C>T (p.Arg118Trp) rs143813189 0.00147
NM_145725.3(TRAF3):c.819+4G>A rs200177742 0.00136
NM_145725.3(TRAF3):c.1194C>T (p.Arg398=) rs151258452 0.00036
NM_145725.3(TRAF3):c.1227G>A (p.Leu409=) rs150483724 0.00011
NM_145725.3(TRAF3):c.933T>C (p.Asn311=) rs780127114 0.00011
NM_145725.3(TRAF3):c.1251G>T (p.Val417=) rs781327389 0.00010
NM_145725.3(TRAF3):c.402+18A>C rs369040491 0.00009
NM_145725.3(TRAF3):c.403-14G>A rs371219336 0.00008
NM_145725.3(TRAF3):c.652-7G>A rs756741999 0.00006
NM_145725.3(TRAF3):c.729G>A (p.Gly243=) rs755678092 0.00006
NM_145725.3(TRAF3):c.1383C>T (p.Asn461=) rs141356642 0.00005
NM_145725.3(TRAF3):c.36G>A (p.Ala12=) rs199639339 0.00005
NM_145725.3(TRAF3):c.1254C>T (p.Leu418=) rs201486992 0.00004
NM_145725.3(TRAF3):c.1389C>T (p.Asp463=) rs752675828 0.00004
NM_145725.3(TRAF3):c.1407G>A (p.Thr469=) rs200974693 0.00004
NM_145725.3(TRAF3):c.1590C>T (p.Ile530=) rs767522694 0.00004
NM_145725.3(TRAF3):c.297+11G>T rs945150600 0.00004
NM_145725.3(TRAF3):c.402+11A>G rs775340536 0.00004
NM_145725.3(TRAF3):c.402+7A>G rs142069424 0.00004
NM_145725.3(TRAF3):c.483C>T (p.Asp161=) rs374166578 0.00004
NM_145725.3(TRAF3):c.652-18G>A rs763625789 0.00004
NM_145725.3(TRAF3):c.652-8C>T rs751024987 0.00004
NM_145725.3(TRAF3):c.727-16A>G rs560306318 0.00004
NM_145725.3(TRAF3):c.777C>T (p.His259=) rs746133902 0.00004
NM_145725.3(TRAF3):c.1245T>C (p.Asn415=) rs1364339851 0.00003
NM_145725.3(TRAF3):c.245+7G>A rs549971853 0.00003
NM_145725.3(TRAF3):c.297+10G>A rs749532785 0.00003
NM_145725.3(TRAF3):c.1113G>A (p.Ala371=) rs761877084 0.00002
NM_145725.3(TRAF3):c.1242C>T (p.Tyr414=) rs747125046 0.00002
NM_145725.3(TRAF3):c.57A>G (p.Leu19=) rs762827715 0.00002
NM_145725.3(TRAF3):c.960+19C>T rs773647944 0.00002
NM_145725.3(TRAF3):c.996G>A (p.Glu332=) rs1217760239 0.00002
NM_145725.3(TRAF3):c.1098C>T (p.Ser366=) rs772951409 0.00001
NM_145725.3(TRAF3):c.1136-15C>T rs746286210 0.00001
NM_145725.3(TRAF3):c.1185C>T (p.His395=) rs376141594 0.00001
NM_145725.3(TRAF3):c.1239C>T (p.Ser413=) rs111762207 0.00001
NM_145725.3(TRAF3):c.1431C>A (p.Ile477=) rs1235902845 0.00001
NM_145725.3(TRAF3):c.1644T>C (p.Tyr548=) rs370725073 0.00001
NM_145725.3(TRAF3):c.210C>T (p.His70=) rs776782540 0.00001
NM_145725.3(TRAF3):c.219C>T (p.Cys73=) rs759871810 0.00001
NM_145725.3(TRAF3):c.245+12C>T rs935055991 0.00001
NM_145725.3(TRAF3):c.315C>T (p.Cys105=) rs1202527418 0.00001
NM_145725.3(TRAF3):c.375A>C (p.Ala125=) rs1327573442 0.00001
NM_145725.3(TRAF3):c.51G>A (p.Pro17=) rs1166121049 0.00001
NM_145725.3(TRAF3):c.564G>C (p.Ala188=) rs1266755441 0.00001
NM_145725.3(TRAF3):c.726+11G>A rs1302799078 0.00001
NM_145725.3(TRAF3):c.727-7C>T rs376963322 0.00001
NM_145725.3(TRAF3):c.765C>T (p.Ser255=) rs779058785 0.00001
NM_145725.3(TRAF3):c.987A>G (p.Lys329=) rs372134660 0.00001
NM_145725.3(TRAF3):c.1086C>T (p.Thr362=)
NM_145725.3(TRAF3):c.111A>G (p.Gly37=)
NM_145725.3(TRAF3):c.1135+12G>C
NM_145725.3(TRAF3):c.1135+15G>A
NM_145725.3(TRAF3):c.1135+17G>T
NM_145725.3(TRAF3):c.1135+20C>T
NM_145725.3(TRAF3):c.1135+4_1135+9dup
NM_145725.3(TRAF3):c.1135+9GGGGCC[3] rs770010784
NM_145725.3(TRAF3):c.1136-10C>T rs2140010162
NM_145725.3(TRAF3):c.1136-17del rs1387336059
NM_145725.3(TRAF3):c.1136-4G>A
NM_145725.3(TRAF3):c.1143G>A (p.Leu381=) rs878904361
NM_145725.3(TRAF3):c.1161G>T (p.Arg387=)
NM_145725.3(TRAF3):c.1200C>T (p.Ala400=) rs370697221
NM_145725.3(TRAF3):c.1233C>G (p.Thr411=)
NM_145725.3(TRAF3):c.1233C>T (p.Thr411=) rs754913006
NM_145725.3(TRAF3):c.1308G>A (p.Lys436=)
NM_145725.3(TRAF3):c.1314G>A (p.Leu438=)
NM_145725.3(TRAF3):c.1317C>G (p.Ser439=) rs1890539980
NM_145725.3(TRAF3):c.1323C>T (p.Tyr441=) rs1159024547
NM_145725.3(TRAF3):c.1377C>T (p.Tyr459=)
NM_145725.3(TRAF3):c.138C>A (p.Thr46=)
NM_145725.3(TRAF3):c.138C>G (p.Thr46=) rs201415483
NM_145725.3(TRAF3):c.138C>T (p.Thr46=) rs201415483
NM_145725.3(TRAF3):c.1398G>T (p.Gly466=)
NM_145725.3(TRAF3):c.1413G>A (p.Leu471=) rs934114383
NM_145725.3(TRAF3):c.1467G>A (p.Pro489=)
NM_145725.3(TRAF3):c.153C>T (p.Tyr51=) rs1165346141
NM_145725.3(TRAF3):c.1551C>T (p.Asn517=)
NM_145725.3(TRAF3):c.1575T>C (p.Thr525=)
NM_145725.3(TRAF3):c.1581G>A (p.Glu527=)
NM_145725.3(TRAF3):c.1599C>G (p.Gly533=)
NM_145725.3(TRAF3):c.1611T>C (p.Phe537=)
NM_145725.3(TRAF3):c.1626T>C (p.Val542=) rs756160197
NM_145725.3(TRAF3):c.165G>A (p.Lys55=) rs1555373885
NM_145725.3(TRAF3):c.1665T>C (p.Phe555=)
NM_145725.3(TRAF3):c.198C>G (p.Thr66=) rs1275435989
NM_145725.3(TRAF3):c.245+11T>A
NM_145725.3(TRAF3):c.245+14C>T
NM_145725.3(TRAF3):c.245+17G>A
NM_145725.3(TRAF3):c.245+17G>T
NM_145725.3(TRAF3):c.245+22_245+33del rs750157259
NM_145725.3(TRAF3):c.246-12_246-11del
NM_145725.3(TRAF3):c.246-14G>T
NM_145725.3(TRAF3):c.246-17C>T rs1888362225
NM_145725.3(TRAF3):c.246-18A>G
NM_145725.3(TRAF3):c.267A>C (p.Thr89=) rs147871145
NM_145725.3(TRAF3):c.270G>A (p.Ala90=) rs149018928
NM_145725.3(TRAF3):c.270G>T (p.Ala90=) rs149018928
NM_145725.3(TRAF3):c.285C>T (p.Ile95=) rs1888365637
NM_145725.3(TRAF3):c.297+21dup rs754443563
NM_145725.3(TRAF3):c.300G>A (p.Val100=)
NM_145725.3(TRAF3):c.318C>T (p.Cys106=)
NM_145725.3(TRAF3):c.345C>A (p.Ile115=)
NM_145725.3(TRAF3):c.386_387inv (p.Met129Thr)
NM_145725.3(TRAF3):c.390G>A (p.Leu130=)
NM_145725.3(TRAF3):c.402+17C>G
NM_145725.3(TRAF3):c.402+17C>T
NM_145725.3(TRAF3):c.402+20T>C
NM_145725.3(TRAF3):c.402+20dup
NM_145725.3(TRAF3):c.486G>T (p.Leu162=) rs1203713349
NM_145725.3(TRAF3):c.501G>A (p.Glu167=) rs1395205435
NM_145725.3(TRAF3):c.507G>A (p.Ala169=)
NM_145725.3(TRAF3):c.507G>C (p.Ala169=) rs145367471
NM_145725.3(TRAF3):c.507G>T (p.Ala169=)
NM_145725.3(TRAF3):c.528A>G (p.Thr176=) rs1440495241
NM_145725.3(TRAF3):c.543G>A (p.Lys181=) rs2139857949
NM_145725.3(TRAF3):c.549G>A (p.Gln183=)
NM_145725.3(TRAF3):c.54G>A (p.Pro18=)
NM_145725.3(TRAF3):c.561C>T (p.Ile187=)
NM_145725.3(TRAF3):c.564G>A (p.Ala188=) rs1266755441
NM_145725.3(TRAF3):c.567G>C (p.Leu189=)
NM_145725.3(TRAF3):c.570+12C>A
NM_145725.3(TRAF3):c.570+18C>G
NM_145725.3(TRAF3):c.570+31_570+66del
NM_145725.3(TRAF3):c.570+9C>T rs1888661155
NM_145725.3(TRAF3):c.652-18G>T rs763625789
NM_145725.3(TRAF3):c.652-19C>T
NM_145725.3(TRAF3):c.711T>C (p.Tyr237=)
NM_145725.3(TRAF3):c.726+16T>G
NM_145725.3(TRAF3):c.727-15T>C
NM_145725.3(TRAF3):c.727-4G>A
NM_145725.3(TRAF3):c.727-4G>T rs750091557
NM_145725.3(TRAF3):c.747G>A (p.Lys249=) rs2139944193
NM_145725.3(TRAF3):c.768C>T (p.Ala256=) rs757652604
NM_145725.3(TRAF3):c.774G>A (p.Gln258=)
NM_145725.3(TRAF3):c.807G>A (p.Ser269=)
NM_145725.3(TRAF3):c.810C>G (p.Leu270=)
NM_145725.3(TRAF3):c.819+16T>C
NM_145725.3(TRAF3):c.819+16dup
NM_145725.3(TRAF3):c.820-12T>C rs2139974257
NM_145725.3(TRAF3):c.825C>T (p.Ser275=)
NM_145725.3(TRAF3):c.840A>G (p.Glu280=)
NM_145725.3(TRAF3):c.858G>A (p.Lys286=)
NM_145725.3(TRAF3):c.87G>A (p.Thr29=)
NM_145725.3(TRAF3):c.90A>G (p.Pro30=)
NM_145725.3(TRAF3):c.957A>G (p.Leu319=)
NM_145725.3(TRAF3):c.960+20G>A rs747491445
NM_145725.3(TRAF3):c.961-11T>G
NM_145725.3(TRAF3):c.961-12T>G
NM_145725.3(TRAF3):c.961-13T>C
NM_145725.3(TRAF3):c.9G>C (p.Ser3=) rs377427517

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.