ClinVar Miner

List of variants in gene TNFSF12, TNFSF12-TNFSF13 studied for Common variable immunodeficiency

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 187
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_003809.3(TNFSF12):c.600G>C (p.Ala200=) rs3803798 0.50487
NM_003809.3(TNFSF12):c.276C>A (p.Arg92=) rs62059804 0.20757
NM_003809.3(TNFSF12):c.642G>T (p.Gly214=) rs4968189 0.01736
NM_003809.3(TNFSF12):c.338-9A>G rs114577645 0.01655
NM_003809.3(TNFSF12):c.597G>A (p.Ala199=) rs143039184 0.00141
NM_003809.3(TNFSF12):c.609C>T (p.Leu203=) rs140608168 0.00140
NM_003809.3(TNFSF12):c.357G>A (p.Gln119=) rs147826685 0.00113
NM_003809.3(TNFSF12):c.160-19G>A rs137994694 0.00069
NM_003809.3(TNFSF12):c.157C>A (p.Gln53Lys) rs532271559 0.00026
NM_003809.3(TNFSF12):c.353G>A (p.Gly118Glu) rs144468031 0.00019
NM_003809.3(TNFSF12):c.443G>A (p.Arg148His) rs200059075 0.00016
NM_003809.3(TNFSF12):c.429T>G (p.Pro143=) rs770924960 0.00012
NM_003809.3(TNFSF12):c.623G>A (p.Arg208His) rs376560567 0.00011
NM_003809.3(TNFSF12):c.450C>T (p.Ile150=) rs147597489 0.00009
NM_003809.3(TNFSF12):c.690C>G (p.Pro230=) rs1237382978 0.00009
NM_003809.3(TNFSF12):c.109C>T (p.Leu37Phe) rs756671729 0.00007
NM_003809.3(TNFSF12):c.729C>T (p.Phe243=) rs200770110 0.00007
NM_003809.3(TNFSF12):c.143C>T (p.Ala48Val) rs1411564411 0.00006
NM_003809.3(TNFSF12):c.365C>T (p.Ala122Val) rs145233196 0.00006
NM_003809.3(TNFSF12):c.374-9C>T rs367612596 0.00006
NM_003809.3(TNFSF12):c.655C>T (p.Arg219Trp) rs764236967 0.00006
NM_003809.3(TNFSF12):c.204G>A (p.Pro68=) rs751381442 0.00005
NM_003809.3(TNFSF12):c.373+18G>A rs370242260 0.00005
NM_003809.3(TNFSF12):c.304C>T (p.Arg102Trp) rs150816164 0.00004
NM_003809.3(TNFSF12):c.374-8G>A rs551460083 0.00004
NM_003809.3(TNFSF12):c.386C>A (p.Thr129Lys) rs746536507 0.00004
NM_003809.3(TNFSF12):c.662G>C (p.Gly221Ala) rs764630895 0.00004
NM_003809.3(TNFSF12):c.142G>C (p.Ala48Pro) rs1368698594 0.00003
NM_003809.3(TNFSF12):c.159+15C>T rs1274339400 0.00003
NM_003809.3(TNFSF12):c.245C>T (p.Ala82Val) rs370085069 0.00003
NM_003809.3(TNFSF12):c.295C>T (p.Arg99Trp) rs748479475 0.00003
NM_003809.3(TNFSF12):c.622C>T (p.Arg208Cys) rs777759037 0.00003
NM_003809.3(TNFSF12):c.679C>T (p.Arg227Cys) rs1414804824 0.00003
NM_003809.3(TNFSF12):c.141G>T (p.Arg47=) rs1167726401 0.00002
NM_003809.3(TNFSF12):c.159+11G>T rs1051286778 0.00002
NM_003809.3(TNFSF12):c.197A>G (p.Gln66Arg) rs1390303105 0.00002
NM_003809.3(TNFSF12):c.321C>T (p.Ile107=) rs139642600 0.00002
NM_003809.3(TNFSF12):c.381C>T (p.Asp127=) rs576803878 0.00002
NM_003809.3(TNFSF12):c.469C>T (p.Arg157Trp) rs763175605 0.00002
NM_003809.3(TNFSF12):c.674G>A (p.Arg225Gln) rs576689580 0.00002
NM_003809.3(TNFSF12):c.716T>C (p.Phe239Ser) rs761947704 0.00002
NM_003809.3(TNFSF12):c.105C>G (p.Leu35=) rs908438555 0.00001
NM_003809.3(TNFSF12):c.134G>A (p.Gly45Glu) rs2070971132 0.00001
NM_003809.3(TNFSF12):c.137G>C (p.Ser46Thr) rs1386396522 0.00001
NM_003809.3(TNFSF12):c.159+7C>A rs535840017 0.00001
NM_003809.3(TNFSF12):c.194A>C (p.Asp65Ala) rs747019973 0.00001
NM_003809.3(TNFSF12):c.208-7C>G rs2070983662 0.00001
NM_003809.3(TNFSF12):c.284C>A (p.Ala95Glu) rs1187061850 0.00001
NM_003809.3(TNFSF12):c.296G>A (p.Arg99Gln) rs770131727 0.00001
NM_003809.3(TNFSF12):c.305G>A (p.Arg102Gln) rs749853561 0.00001
NM_003809.3(TNFSF12):c.310C>T (p.Arg104Ter) rs1432703775 0.00001
NM_003809.3(TNFSF12):c.318G>A (p.Ala106=) rs764045774 0.00001
NM_003809.3(TNFSF12):c.326C>T (p.Ala109Val) rs1207281513 0.00001
NM_003809.3(TNFSF12):c.337+12G>A rs1367179093 0.00001
NM_003809.3(TNFSF12):c.337+14G>A rs751618286 0.00001
NM_003809.3(TNFSF12):c.337+5G>A rs1196455086 0.00001
NM_003809.3(TNFSF12):c.374G>A (p.Gly125Asp) rs765689290 0.00001
NM_003809.3(TNFSF12):c.433C>T (p.Arg145Cys) rs540997935 0.00001
NM_003809.3(TNFSF12):c.442C>T (p.Arg148Cys) rs764223156 0.00001
NM_003809.3(TNFSF12):c.499-10C>T rs1323154572 0.00001
NM_003809.3(TNFSF12):c.529C>T (p.Leu177=) rs1239258225 0.00001
NM_003809.3(TNFSF12):c.554G>A (p.Gly185Asp) rs149050050 0.00001
NM_003809.3(TNFSF12):c.569G>A (p.Arg190His) rs1191670290 0.00001
NM_003809.3(TNFSF12):c.596C>T (p.Ala199Val) rs753366720 0.00001
NM_003809.3(TNFSF12):c.663G>T (p.Gly221=) rs776034989 0.00001
NC_000017.10:g.(?_7452471)_(7454315_?)dup
NM_003809.3(TNFSF12):c.105C>T (p.Leu35=) rs908438555
NM_003809.3(TNFSF12):c.106G>A (p.Gly36Ser) rs2070970743
NM_003809.3(TNFSF12):c.108C>T (p.Gly36=) rs2150904074
NM_003809.3(TNFSF12):c.109del (p.Leu37fs)
NM_003809.3(TNFSF12):c.11G>C (p.Arg4Pro)
NM_003809.3(TNFSF12):c.120C>T (p.Ala40=)
NM_003809.3(TNFSF12):c.128G>A (p.Ser43Asn) rs2150904090
NM_003809.3(TNFSF12):c.139C>G (p.Arg47Gly)
NM_003809.3(TNFSF12):c.139C>T (p.Arg47Trp)
NM_003809.3(TNFSF12):c.147G>A (p.Ser49=) rs1036232885
NM_003809.3(TNFSF12):c.154G>A (p.Ala52Thr) rs2070971587
NM_003809.3(TNFSF12):c.159+3G>A
NM_003809.3(TNFSF12):c.159+5G>C rs200575102
NM_003809.3(TNFSF12):c.159+7C>T rs535840017
NM_003809.3(TNFSF12):c.160-14C>T
NM_003809.3(TNFSF12):c.160-16C>T
NM_003809.3(TNFSF12):c.160-21_160-17del
NM_003809.3(TNFSF12):c.164C>T (p.Pro55Leu) rs764718533
NM_003809.3(TNFSF12):c.177G>C (p.Glu59Asp) rs868687352
NM_003809.3(TNFSF12):c.186A>G (p.Ala62=) rs2150904254
NM_003809.3(TNFSF12):c.187G>A (p.Glu63Lys)
NM_003809.3(TNFSF12):c.189GGA[1] (p.Glu64del) rs2150904255
NM_003809.3(TNFSF12):c.190G>A (p.Glu64Lys)
NM_003809.3(TNFSF12):c.196C>T (p.Gln66Ter)
NM_003809.3(TNFSF12):c.201C>A (p.Asp67Glu)
NM_003809.3(TNFSF12):c.205_207dup (p.Ser69dup) rs753259588
NM_003809.3(TNFSF12):c.207+10C>T
NM_003809.3(TNFSF12):c.207+11G>A rs1266540123
NM_003809.3(TNFSF12):c.207+14G>A
NM_003809.3(TNFSF12):c.207+17G>A
NM_003809.3(TNFSF12):c.207+18C>T
NM_003809.3(TNFSF12):c.207+19G>A
NM_003809.3(TNFSF12):c.207+3G>C
NM_003809.3(TNFSF12):c.208-15C>T
NM_003809.3(TNFSF12):c.208-19C>G
NM_003809.3(TNFSF12):c.208-3T>C
NM_003809.3(TNFSF12):c.208-8T>A rs2150904642
NM_003809.3(TNFSF12):c.219C>G (p.Pro73=) rs2150904657
NM_003809.3(TNFSF12):c.222G>C (p.Gln74His) rs2070984006
NM_003809.3(TNFSF12):c.242C>T (p.Pro81Leu)
NM_003809.3(TNFSF12):c.243T>C (p.Pro81=)
NM_003809.3(TNFSF12):c.246G>A (p.Ala82=)
NM_003809.3(TNFSF12):c.247C>A (p.Pro83Thr)
NM_003809.3(TNFSF12):c.249T>C (p.Pro83=)
NM_003809.3(TNFSF12):c.258C>T (p.Asn86=)
NM_003809.3(TNFSF12):c.259C>T (p.Arg87Ter)
NM_003809.3(TNFSF12):c.266T>C (p.Val89Ala) rs2070984742
NM_003809.3(TNFSF12):c.269G>A (p.Arg90Gln) rs745967426
NM_003809.3(TNFSF12):c.274C>G (p.Arg92Gly)
NM_003809.3(TNFSF12):c.274C>T (p.Arg92Cys) rs758492571
NM_003809.3(TNFSF12):c.275_276delinsAA (p.Arg92Gln) rs2070984989
NM_003809.3(TNFSF12):c.284-3C>T
NM_003809.3(TNFSF12):c.288T>G (p.Pro96=)
NM_003809.3(TNFSF12):c.295C>G (p.Arg99Gly)
NM_003809.3(TNFSF12):c.310C>G (p.Arg104Gly)
NM_003809.3(TNFSF12):c.312A>G (p.Arg104=) rs1326993093
NM_003809.3(TNFSF12):c.316G>A (p.Ala106Thr)
NM_003809.3(TNFSF12):c.317C>T (p.Ala106Val) rs369851985
NM_003809.3(TNFSF12):c.323C>T (p.Ala108Val)
NM_003809.3(TNFSF12):c.337+16G>A
NM_003809.3(TNFSF12):c.337+7G>A
NM_003809.3(TNFSF12):c.347G>A (p.Arg116Gln) rs771459468
NM_003809.3(TNFSF12):c.350C>A (p.Pro117His)
NM_003809.3(TNFSF12):c.358G>A (p.Asp120Asn)
NM_003809.3(TNFSF12):c.360C>T (p.Asp120=)
NM_003809.3(TNFSF12):c.361G>A (p.Gly121Arg)
NM_003809.3(TNFSF12):c.364G>A (p.Ala122Thr) rs2070995050
NM_003809.3(TNFSF12):c.366G>A (p.Ala122=) rs529570679
NM_003809.3(TNFSF12):c.373+17C>T
NM_003809.3(TNFSF12):c.373+18G>T
NM_003809.3(TNFSF12):c.375T>G (p.Gly125=)
NM_003809.3(TNFSF12):c.376G>A (p.Val126Met)
NM_003809.3(TNFSF12):c.384G>A (p.Gly128=) rs1486694236
NM_003809.3(TNFSF12):c.393T>C (p.Ser131=)
NM_003809.3(TNFSF12):c.398G>A (p.Trp133Ter) rs2150909054
NM_003809.3(TNFSF12):c.402G>A (p.Glu134=)
NM_003809.3(TNFSF12):c.412A>C (p.Ile138Leu)
NM_003809.3(TNFSF12):c.417C>T (p.Asn139=)
NM_003809.3(TNFSF12):c.434G>A (p.Arg145His) rs1295184449
NM_003809.3(TNFSF12):c.438C>T (p.Tyr146=)
NM_003809.3(TNFSF12):c.440A>T (p.Asn147Ile) rs371762842
NM_003809.3(TNFSF12):c.441C>T (p.Asn147=) rs2150909109
NM_003809.3(TNFSF12):c.451G>A (p.Gly151Arg)
NM_003809.3(TNFSF12):c.454G>A (p.Glu152Lys)
NM_003809.3(TNFSF12):c.465C>T (p.Val155=)
NM_003809.3(TNFSF12):c.470G>A (p.Arg157Gln)
NM_003809.3(TNFSF12):c.498+12C>G
NM_003809.3(TNFSF12):c.498+7C>T
NM_003809.3(TNFSF12):c.498+9del rs1356188583
NM_003809.3(TNFSF12):c.499-4C>T rs993444940
NM_003809.3(TNFSF12):c.499-8del
NM_003809.3(TNFSF12):c.503A>C (p.His168Pro)
NM_003809.3(TNFSF12):c.506T>C (p.Phe169Ser)
NM_003809.3(TNFSF12):c.528C>A (p.Tyr176Ter)
NM_003809.3(TNFSF12):c.535C>T (p.Leu179=) rs2150909482
NM_003809.3(TNFSF12):c.563C>T (p.Ala188Val) rs2071082084
NM_003809.3(TNFSF12):c.569G>C (p.Arg190Pro) rs1191670290
NM_003809.3(TNFSF12):c.573C>T (p.Cys191=)
NM_003809.3(TNFSF12):c.576GGA[1] (p.Glu194del) rs2150909548
NM_003809.3(TNFSF12):c.600G>A (p.Ala200=)
NM_003809.3(TNFSF12):c.607C>T (p.Leu203Phe)
NM_003809.3(TNFSF12):c.609C>G (p.Leu203=) rs140608168
NM_003809.3(TNFSF12):c.610G>A (p.Gly204Arg) rs746979506
NM_003809.3(TNFSF12):c.610G>C (p.Gly204Arg)
NM_003809.3(TNFSF12):c.624C>A (p.Arg208=)
NM_003809.3(TNFSF12):c.629G>T (p.Cys210Phe)
NM_003809.3(TNFSF12):c.642= (p.Gly214=)
NM_003809.3(TNFSF12):c.651C>T (p.Ala217=)
NM_003809.3(TNFSF12):c.655C>G (p.Arg219Gly)
NM_003809.3(TNFSF12):c.657G>A (p.Arg219=)
NM_003809.3(TNFSF12):c.657G>T (p.Arg219=) rs1363429844
NM_003809.3(TNFSF12):c.673C>A (p.Arg225=) rs761260715
NM_003809.3(TNFSF12):c.673C>T (p.Arg225Trp) rs761260715
NM_003809.3(TNFSF12):c.680G>A (p.Arg227His)
NM_003809.3(TNFSF12):c.687C>T (p.Leu229=)
NM_003809.3(TNFSF12):c.691T>C (p.Trp231Arg) rs2071085086
NM_003809.3(TNFSF12):c.707C>T (p.Ala236Val) rs2071085410
NM_003809.3(TNFSF12):c.713C>G (p.Pro238Arg)
NM_003809.3(TNFSF12):c.718C>T (p.Leu240Phe)
NM_003809.3(TNFSF12):c.730G>A (p.Gly244Arg)
NM_003809.3(TNFSF12):c.739C>A (p.Gln247Lys)

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.