ClinVar Miner

List of variants in gene TNFRSF1A reported as likely benign for immune system disorder

Included ClinVar conditions (908):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 170
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_001065.4(TNFRSF1A):c.*387A>G rs115682467 0.00805
NM_001065.4(TNFRSF1A):c.224C>T (p.Pro75Leu) rs4149637 0.00574
NM_001065.4(TNFRSF1A):c.1110C>T (p.Arg370=) rs201683984 0.00236
NM_001065.4(TNFRSF1A):c.935G>A (p.Arg312Lys) rs200900510 0.00113
NM_001065.4(TNFRSF1A):c.789T>C (p.Thr263=) rs201290189 0.00069
NM_001065.4(TNFRSF1A):c.769-3C>T rs199743143 0.00054
NM_001065.4(TNFRSF1A):c.839C>A (p.Thr280Asn) rs201399382 0.00041
NM_001065.4(TNFRSF1A):c.193+6G>A rs147111217 0.00037
NM_001065.4(TNFRSF1A):c.369C>T (p.Thr123=) rs104895260 0.00036
NM_001065.4(TNFRSF1A):c.1058-4G>A rs369451569 0.00026
NM_001065.4(TNFRSF1A):c.988G>A (p.Ala330Thr) rs200029309 0.00026
NM_001065.4(TNFRSF1A):c.645C>T (p.Pro215=) rs147075345 0.00020
NM_001065.4(TNFRSF1A):c.1206C>T (p.Ser402=) rs148334665 0.00018
NM_001065.4(TNFRSF1A):c.452A>G (p.Asn151Ser) rs369875050 0.00015
NM_001065.4(TNFRSF1A):c.551+18C>A rs368670172 0.00015
NM_001065.4(TNFRSF1A):c.147T>C (p.Tyr49=) rs150511666 0.00014
NM_001065.4(TNFRSF1A):c.1058-6C>G rs761155688 0.00011
NM_001065.4(TNFRSF1A):c.1328G>T (p.Gly443Val) rs201062001 0.00011
NM_001065.4(TNFRSF1A):c.459C>T (p.Thr153=) rs199792034 0.00011
NM_001065.4(TNFRSF1A):c.596T>C (p.Ile199Thr) rs104895247 0.00011
NM_001065.4(TNFRSF1A):c.249G>A (p.Glu83=) rs104895265 0.00010
NM_001065.4(TNFRSF1A):c.887G>C (p.Ser296Thr) rs770324989 0.00009
NM_001065.4(TNFRSF1A):c.473-16G>A rs104895251 0.00008
NM_001065.4(TNFRSF1A):c.1312G>A (p.Glu438Lys) rs745814061 0.00007
NM_001065.4(TNFRSF1A):c.1197G>T (p.Ala399=) rs140486890 0.00006
NM_001065.4(TNFRSF1A):c.255G>C (p.Glu85Asp) rs770439546 0.00006
NM_001065.4(TNFRSF1A):c.531C>T (p.Asn177=) rs138918985 0.00006
NM_001065.4(TNFRSF1A):c.672T>C (p.Leu224=) rs202150552 0.00006
NM_001065.4(TNFRSF1A):c.784A>G (p.Thr262Ala) rs200728879 0.00006
NM_001065.4(TNFRSF1A):c.168G>A (p.Ser56=) rs104895280 0.00005
NM_001065.4(TNFRSF1A):c.434A>G (p.Asn145Ser) rs104895288 0.00005
NM_001065.4(TNFRSF1A):c.194-15C>T rs104895259 0.00003
NM_001065.4(TNFRSF1A):c.339G>A (p.Glu113=) rs587780965 0.00003
NM_001065.4(TNFRSF1A):c.492C>T (p.Thr164=) rs373422284 0.00003
NM_001065.4(TNFRSF1A):c.1002C>T (p.Ile334=) rs748720159 0.00002
NM_001065.4(TNFRSF1A):c.1083C>G (p.Ala361=) rs746923911 0.00002
NM_001065.4(TNFRSF1A):c.1233G>A (p.Thr411=) rs1176222642 0.00002
NM_001065.4(TNFRSF1A):c.1257G>A (p.Glu419=) rs199636425 0.00002
NM_001065.4(TNFRSF1A):c.1343C>T (p.Pro448Leu) rs1289887403 0.00002
NM_001065.4(TNFRSF1A):c.193+18C>T rs757177584 0.00002
NM_001065.4(TNFRSF1A):c.228G>A (p.Gly76=) rs104895274 0.00002
NM_001065.4(TNFRSF1A):c.243C>T (p.Cys81=) rs56002980 0.00002
NM_001065.4(TNFRSF1A):c.549T>C (p.Ser183=) rs200963205 0.00002
NM_001065.4(TNFRSF1A):c.558G>A (p.Lys186=) rs104895275 0.00002
NM_001065.4(TNFRSF1A):c.1005C>T (p.Pro335=) rs1399868027 0.00001
NM_001065.4(TNFRSF1A):c.1008C>A (p.Asn336Lys) rs745458338 0.00001
NM_001065.4(TNFRSF1A):c.1012C>T (p.Leu338Phe) rs1251500082 0.00001
NM_001065.4(TNFRSF1A):c.1035C>T (p.Ala345=) rs1323382829 0.00001
NM_001065.4(TNFRSF1A):c.1037A>G (p.His346Arg) rs1399104304 0.00001
NM_001065.4(TNFRSF1A):c.1058-12G>A rs776610155 0.00001
NM_001065.4(TNFRSF1A):c.1058-8C>G rs764636915 0.00001
NM_001065.4(TNFRSF1A):c.12C>T (p.Ser4=) rs199780452 0.00001
NM_001065.4(TNFRSF1A):c.1323T>C (p.Leu441=) rs1565465505 0.00001
NM_001065.4(TNFRSF1A):c.1329C>A (p.Gly443=) rs756455040 0.00001
NM_001065.4(TNFRSF1A):c.1363A>C (p.Arg455=) rs1236501292 0.00001
NM_001065.4(TNFRSF1A):c.225G>A (p.Pro75=) rs771721939 0.00001
NM_001065.4(TNFRSF1A):c.258C>T (p.Ser86=) rs201798720 0.00001
NM_001065.4(TNFRSF1A):c.269C>T (p.Thr90Ile) rs34751757 0.00001
NM_001065.4(TNFRSF1A):c.270C>T (p.Thr90=) rs200837112 0.00001
NM_001065.4(TNFRSF1A):c.31C>T (p.Leu11=) rs1195086731 0.00001
NM_001065.4(TNFRSF1A):c.384G>A (p.Arg128=) rs747164054 0.00001
NM_001065.4(TNFRSF1A):c.414A>G (p.Glu138=) rs201862823 0.00001
NM_001065.4(TNFRSF1A):c.473-17C>T rs202031171 0.00001
NM_001065.4(TNFRSF1A):c.482A>G (p.Lys161Arg) rs578112440 0.00001
NM_001065.4(TNFRSF1A):c.51G>A (p.Glu17=) rs201015273 0.00001
NM_001065.4(TNFRSF1A):c.552-12C>A rs1208890021 0.00001
NM_001065.4(TNFRSF1A):c.552-14G>A rs200381667 0.00001
NM_001065.4(TNFRSF1A):c.570G>A (p.Glu190=) rs772273430 0.00001
NM_001065.4(TNFRSF1A):c.696A>G (p.Leu232=) rs1433705996 0.00001
NM_001065.4(TNFRSF1A):c.792T>C (p.Thr264=) rs113540488 0.00001
NM_001065.4(TNFRSF1A):c.1018A>G (p.Lys340Glu) rs778653907
NM_001065.4(TNFRSF1A):c.102A>G (p.Leu34=)
NM_001065.4(TNFRSF1A):c.1057+14G>A
NM_001065.4(TNFRSF1A):c.1057+16G>A rs1478588008
NM_001065.4(TNFRSF1A):c.1057+16_1057+18dup
NM_001065.4(TNFRSF1A):c.1057+18C>T rs1948011690
NM_001065.4(TNFRSF1A):c.1058-13C>T rs1358132747
NM_001065.4(TNFRSF1A):c.1058-15C>T
NM_001065.4(TNFRSF1A):c.1058-17G>A
NM_001065.4(TNFRSF1A):c.1058-4G>C rs369451569
NM_001065.4(TNFRSF1A):c.1058-5C>G rs1948006524
NM_001065.4(TNFRSF1A):c.1058-5C>T rs1948006524
NM_001065.4(TNFRSF1A):c.1058-8C>T
NM_001065.4(TNFRSF1A):c.1058-9T>C rs899753301
NM_001065.4(TNFRSF1A):c.1083C>T (p.Ala361=) rs746923911
NM_001065.4(TNFRSF1A):c.1126C>A (p.Arg376=)
NM_001065.4(TNFRSF1A):c.1140G>A (p.Leu380=)
NM_001065.4(TNFRSF1A):c.1170G>T (p.Leu390=)
NM_001065.4(TNFRSF1A):c.1191C>G (p.Arg397=)
NM_001065.4(TNFRSF1A):c.1197G>A (p.Ala399=)
NM_001065.4(TNFRSF1A):c.1233G>C (p.Thr411=)
NM_001065.4(TNFRSF1A):c.123T>C (p.Asp41=) rs104895271
NM_001065.4(TNFRSF1A):c.1251G>T (p.Thr417=) rs200473080
NM_001065.4(TNFRSF1A):c.1254G>A (p.Leu418=)
NM_001065.4(TNFRSF1A):c.1287C>T (p.Asp429=) rs1592043048
NM_001065.4(TNFRSF1A):c.1320G>A (p.Ala440=) rs980022194
NM_001065.4(TNFRSF1A):c.1341C>T (p.Leu447=) rs2136811931
NM_001065.4(TNFRSF1A):c.1344G>A (p.Pro448=) rs201538598
NM_001065.4(TNFRSF1A):c.1344G>T (p.Pro448=) rs201538598
NM_001065.4(TNFRSF1A):c.1359T>G (p.Leu453=)
NM_001065.4(TNFRSF1A):c.1367G>A (p.Ter456=)
NM_001065.4(TNFRSF1A):c.150C>T (p.Ile50=)
NM_001065.4(TNFRSF1A):c.193+20G>A
NM_001065.4(TNFRSF1A):c.193+7G>A
NM_001065.4(TNFRSF1A):c.193+9A>C rs2136823017
NM_001065.4(TNFRSF1A):c.194-8A>G
NM_001065.4(TNFRSF1A):c.213C>T (p.Asp71=)
NM_001065.4(TNFRSF1A):c.237G>A (p.Thr79=)
NM_001065.4(TNFRSF1A):c.237G>C (p.Thr79=)
NM_001065.4(TNFRSF1A):c.24C>T (p.Asp8=)
NM_001065.4(TNFRSF1A):c.318A>G (p.Arg106=) rs1948082518
NM_001065.4(TNFRSF1A):c.322+15G>T
NM_001065.4(TNFRSF1A):c.322+19G>A
NM_001065.4(TNFRSF1A):c.323-17T>C rs2136822053
NM_001065.4(TNFRSF1A):c.323-18A>G
NM_001065.4(TNFRSF1A):c.369C>G (p.Thr123=)
NM_001065.4(TNFRSF1A):c.397C>A (p.Arg133=)
NM_001065.4(TNFRSF1A):c.40-13G>T
NM_001065.4(TNFRSF1A):c.40-19C>A rs200226574
NM_001065.4(TNFRSF1A):c.40-19C>T
NM_001065.4(TNFRSF1A):c.40-6C>T
NM_001065.4(TNFRSF1A):c.40-9C>A rs371080583
NM_001065.4(TNFRSF1A):c.462G>A (p.Val154=) rs768460687
NM_001065.4(TNFRSF1A):c.472+7G>A
NM_001065.4(TNFRSF1A):c.472+7G>T rs200194581
NM_001065.4(TNFRSF1A):c.473-4A>G rs2136821321
NM_001065.4(TNFRSF1A):c.473-5T>A
NM_001065.4(TNFRSF1A):c.473-7C>T
NM_001065.4(TNFRSF1A):c.546T>C (p.Cys182=)
NM_001065.4(TNFRSF1A):c.54G>C (p.Leu18=) rs1454940336
NM_001065.4(TNFRSF1A):c.552-16C>T
NM_001065.4(TNFRSF1A):c.576G>C (p.Thr192=)
NM_001065.4(TNFRSF1A):c.57G>A (p.Leu19=) rs1948090257
NM_001065.4(TNFRSF1A):c.580T>C (p.Leu194=) rs2136817802
NM_001065.4(TNFRSF1A):c.60G>A (p.Val20=) rs778929455
NM_001065.4(TNFRSF1A):c.625+10del
NM_001065.4(TNFRSF1A):c.625+18G>A
NM_001065.4(TNFRSF1A):c.626-13G>A
NM_001065.4(TNFRSF1A):c.626-18C>T
NM_001065.4(TNFRSF1A):c.627C>T (p.Gly209=)
NM_001065.4(TNFRSF1A):c.630C>A (p.Thr210=) rs1948038905
NM_001065.4(TNFRSF1A):c.639G>A (p.Leu213=)
NM_001065.4(TNFRSF1A):c.646C>T (p.Leu216=) rs2136817386
NM_001065.4(TNFRSF1A):c.660T>C (p.Phe220=)
NM_001065.4(TNFRSF1A):c.684C>T (p.Leu228=)
NM_001065.4(TNFRSF1A):c.713G>A (p.Arg238Gln)
NM_001065.4(TNFRSF1A):c.714G>A (p.Arg238=) rs200376188
NM_001065.4(TNFRSF1A):c.732C>T (p.Tyr244=)
NM_001065.4(TNFRSF1A):c.739+10G>A
NM_001065.4(TNFRSF1A):c.769-11C>G
NM_001065.4(TNFRSF1A):c.769-11C>T rs765062522
NM_001065.4(TNFRSF1A):c.769-12T>A rs1948022499
NM_001065.4(TNFRSF1A):c.769-19G>A
NM_001065.4(TNFRSF1A):c.769-19G>T
NM_001065.4(TNFRSF1A):c.769-9C>G
NM_001065.4(TNFRSF1A):c.771G>A (p.Gly257=) rs2136815511
NM_001065.4(TNFRSF1A):c.783A>T (p.Gly261=) rs747167733
NM_001065.4(TNFRSF1A):c.78G>A (p.Gly26=)
NM_001065.4(TNFRSF1A):c.828T>C (p.Thr276=)
NM_001065.4(TNFRSF1A):c.834C>T (p.Gly278=)
NM_001065.4(TNFRSF1A):c.843C>A (p.Pro281=)
NM_001065.4(TNFRSF1A):c.847C>T (p.Leu283=)
NM_001065.4(TNFRSF1A):c.861C>G (p.Pro287=)
NM_001065.4(TNFRSF1A):c.903C>G (p.Pro301=) rs1338450773
NM_001065.4(TNFRSF1A):c.924G>A (p.Ala308=) rs2136814745
NM_001065.4(TNFRSF1A):c.927T>G (p.Ala309=)
NM_001065.4(TNFRSF1A):c.943G>A (p.Ala315Thr)
NM_001065.4(TNFRSF1A):c.960G>A (p.Gly320=) rs868081847
NM_001065.4(TNFRSF1A):c.993C>G (p.Ser331=) rs1352725854
NM_001065.4(TNFRSF1A):c.9C>T (p.Leu3=)

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.