ClinVar Miner

List of variants in gene TNFRSF13B reported as uncertain significance for immune system disorder

Included ClinVar conditions (908):
Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 171
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HGVS dbSNP gnomAD frequency
NM_012452.3(TNFRSF13B):c.310T>C (p.Cys104Arg) rs34557412 0.00403
NM_012452.3(TNFRSF13B):c.604C>T (p.Arg202Cys) rs143562358 0.00036
NM_012452.3(TNFRSF13B):c.468T>G (p.Ser156Arg) rs148758686 0.00035
NM_012452.3(TNFRSF13B):c.260T>A (p.Ile87Asn) rs72553877 0.00034
NM_012452.3(TNFRSF13B):c.754G>A (p.Asp252Asn) rs111439115 0.00031
NM_012452.3(TNFRSF13B):c.641T>C (p.Met214Thr) rs144560464 0.00027
NM_012452.3(TNFRSF13B):c.145T>C (p.Ser49Pro) rs374547688 0.00023
NM_012452.3(TNFRSF13B):c.828C>G (p.Asp276Glu) rs144383122 0.00023
NM_012452.3(TNFRSF13B):c.41G>A (p.Arg14His) rs200309474 0.00022
NM_012452.3(TNFRSF13B):c.236A>G (p.Tyr79Cys) rs72553876 0.00021
NM_012452.3(TNFRSF13B):c.515G>A (p.Cys172Tyr) rs751216929 0.00020
NM_012452.3(TNFRSF13B):c.171G>C (p.Gln57His) rs149084717 0.00018
NM_012452.3(TNFRSF13B):c.592C>T (p.Arg198Cys) rs140781824 0.00016
NM_012452.3(TNFRSF13B):c.512T>G (p.Leu171Arg) rs143027621 0.00012
NM_012452.3(TNFRSF13B):c.58C>T (p.Arg20Cys) rs200013015 0.00012
NM_012452.3(TNFRSF13B):c.797C>T (p.Thr266Ile) rs752825527 0.00011
NM_012452.3(TNFRSF13B):c.706G>T (p.Glu236Ter) rs201021960 0.00010
NM_012452.3(TNFRSF13B):c.577T>C (p.Cys193Arg) rs764125338 0.00009
NM_012452.3(TNFRSF13B):c.823C>T (p.Pro275Ser) rs540918755 0.00008
NM_012452.3(TNFRSF13B):c.118T>C (p.Trp40Arg) rs72553874 0.00007
NM_012452.3(TNFRSF13B):c.34C>T (p.Arg12Trp) rs779924436 0.00006
NM_012452.3(TNFRSF13B):c.364C>T (p.Arg122Trp) rs201124889 0.00006
NM_012452.3(TNFRSF13B):c.452C>T (p.Pro151Leu) rs200037919 0.00006
NM_012452.3(TNFRSF13B):c.593G>A (p.Arg198His) rs150974807 0.00006
NM_012452.3(TNFRSF13B):c.637G>A (p.Ala213Thr) rs140914723 0.00006
NM_012452.3(TNFRSF13B):c.740C>T (p.Thr247Met) rs149635611 0.00006
NM_012452.3(TNFRSF13B):c.779G>A (p.Gly260Glu) rs150660451 0.00006
NM_012452.3(TNFRSF13B):c.59G>A (p.Arg20His) rs768682333 0.00005
NM_012452.3(TNFRSF13B):c.61+5G>A rs374249932 0.00005
NM_012452.3(TNFRSF13B):c.716C>T (p.Ala239Val) rs375891337 0.00005
NM_012452.3(TNFRSF13B):c.17G>A (p.Arg6Gln) rs747078163 0.00004
NM_012452.3(TNFRSF13B):c.214C>T (p.Arg72Cys) rs375514495 0.00004
NM_012452.3(TNFRSF13B):c.35G>A (p.Arg12Gln) rs754315707 0.00004
NM_012452.3(TNFRSF13B):c.704_705del (p.Pro235fs) rs749017984 0.00004
NM_012452.3(TNFRSF13B):c.122A>G (p.Asp41Gly) rs763197017 0.00003
NM_012452.3(TNFRSF13B):c.251G>C (p.Arg84Thr) rs747863360 0.00003
NM_012452.3(TNFRSF13B):c.26G>A (p.Arg9Gln) rs772399974 0.00003
NM_012452.3(TNFRSF13B):c.453G>C (p.Pro151=) rs768819413 0.00003
NM_012452.3(TNFRSF13B):c.566G>T (p.Arg189Met) rs199777698 0.00003
NM_012452.3(TNFRSF13B):c.693C>G (p.Ser231Arg) rs145711865 0.00003
NM_012452.3(TNFRSF13B):c.785A>T (p.His262Leu) rs753296393 0.00003
NM_012452.3(TNFRSF13B):c.179G>A (p.Arg60His) rs373134429 0.00002
NM_012452.3(TNFRSF13B):c.283C>G (p.Gln95Glu) rs549493928 0.00002
NM_012452.3(TNFRSF13B):c.346C>A (p.Pro116Thr) rs757399024 0.00002
NM_012452.3(TNFRSF13B):c.443C>T (p.Pro148Leu) rs200173159 0.00002
NM_012452.3(TNFRSF13B):c.572dup (p.Asp191fs) rs769165409 0.00002
NM_012452.3(TNFRSF13B):c.692G>T (p.Ser231Ile) rs1416340010 0.00002
NM_012452.3(TNFRSF13B):c.76T>C (p.Trp26Arg) rs773591883 0.00002
NM_012452.3(TNFRSF13B):c.787A>G (p.Thr263Ala) rs768133177 0.00002
NM_012452.3(TNFRSF13B):c.132G>A (p.Leu44=) rs200936104 0.00001
NM_012452.3(TNFRSF13B):c.178C>T (p.Arg60Cys) rs777555444 0.00001
NM_012452.3(TNFRSF13B):c.182C>T (p.Thr61Ile) rs752511316 0.00001
NM_012452.3(TNFRSF13B):c.199+4A>G rs370453774 0.00001
NM_012452.3(TNFRSF13B):c.241C>A (p.His81Asn) rs769360883 0.00001
NM_012452.3(TNFRSF13B):c.266G>A (p.Cys89Tyr) rs746779126 0.00001
NM_012452.3(TNFRSF13B):c.275T>A (p.Ile92Asn) rs368250378 0.00001
NM_012452.3(TNFRSF13B):c.290C>G (p.Pro97Arg) rs754139414 0.00001
NM_012452.3(TNFRSF13B):c.350A>G (p.Glu117Gly) rs1159836375 0.00001
NM_012452.3(TNFRSF13B):c.356G>A (p.Arg119Lys) rs1432445886 0.00001
NM_012452.3(TNFRSF13B):c.357G>C (p.Arg119Ser) rs374322117 0.00001
NM_012452.3(TNFRSF13B):c.365G>A (p.Arg122Gln) rs755343222 0.00001
NM_012452.3(TNFRSF13B):c.377T>C (p.Val126Ala) rs1330415205 0.00001
NM_012452.3(TNFRSF13B):c.40C>T (p.Arg14Cys) rs370503383 0.00001
NM_012452.3(TNFRSF13B):c.418G>A (p.Glu140Lys) rs199578237 0.00001
NM_012452.3(TNFRSF13B):c.467G>A (p.Ser156Asn) rs772365135 0.00001
NM_012452.3(TNFRSF13B):c.545T>G (p.Val182Gly) rs774782734 0.00001
NM_012452.3(TNFRSF13B):c.554T>G (p.Phe185Cys) rs778227535 0.00001
NM_012452.3(TNFRSF13B):c.564G>C (p.Lys188Asn) rs2087500993 0.00001
NM_012452.3(TNFRSF13B):c.567G>C (p.Arg189Ser) rs370856157 0.00001
NM_012452.3(TNFRSF13B):c.584G>T (p.Cys195Phe) rs771332658 0.00001
NM_012452.3(TNFRSF13B):c.612T>G (p.Ser204Arg) rs2087500053 0.00001
NM_012452.3(TNFRSF13B):c.631G>C (p.Asp211His) rs955888263 0.00001
NM_012452.3(TNFRSF13B):c.638C>T (p.Ala213Val) rs763164041 0.00001
NM_012452.3(TNFRSF13B):c.639del (p.Met214fs) rs964576531 0.00001
NM_012452.3(TNFRSF13B):c.649G>A (p.Gly217Ser) rs567602037 0.00001
NM_012452.3(TNFRSF13B):c.722C>T (p.Thr241Met) rs370250196 0.00001
NM_012452.3(TNFRSF13B):c.776G>A (p.Trp259Ter) rs764387835 0.00001
NM_012452.3(TNFRSF13B):c.838G>C (p.Gly280Arg) rs374957601 0.00001
NM_012452.3(TNFRSF13B):c.83G>A (p.Gly28Glu) rs1364325591 0.00001
NC_000017.10:g.(?_16842841)_(16875409_?)dup
NC_000017.10:g.(?_16842861)_(16843845_?)dup
NC_000017.10:g.(?_16842861)_(16875389_?)dup
NC_000017.10:g.(?_16855740)_(16855917_?)dup
NC_000017.10:g.(?_16875309)_(16875389_?)dup
NM_012452.3(TNFRSF13B):c.106G>A (p.Glu36Lys)
NM_012452.3(TNFRSF13B):c.109G>C (p.Glu37Gln)
NM_012452.3(TNFRSF13B):c.121G>A (p.Asp41Asn) rs67951770
NM_012452.3(TNFRSF13B):c.121G>C (p.Asp41His) rs67951770
NM_012452.3(TNFRSF13B):c.131T>C (p.Leu44Pro)
NM_012452.3(TNFRSF13B):c.141C>T (p.Cys47=)
NM_012452.3(TNFRSF13B):c.146C>T (p.Ser49Phe)
NM_012452.3(TNFRSF13B):c.149G>C (p.Cys50Ser)
NM_012452.3(TNFRSF13B):c.155C>T (p.Thr52Ile) rs1294881198
NM_012452.3(TNFRSF13B):c.16C>T (p.Arg6Trp) rs768911609
NM_012452.3(TNFRSF13B):c.199+5G>C
NM_012452.3(TNFRSF13B):c.201G>C (p.Arg67Ser) rs886052653
NM_012452.3(TNFRSF13B):c.215G>T (p.Arg72Leu) rs55916807
NM_012452.3(TNFRSF13B):c.21C>G (p.Ser7Arg) rs780461208
NM_012452.3(TNFRSF13B):c.21C>T (p.Ser7=) rs780461208
NM_012452.3(TNFRSF13B):c.226G>T (p.Gly76Cys) rs146436713
NM_012452.3(TNFRSF13B):c.227G>A (p.Gly76Asp) rs772701872
NM_012452.3(TNFRSF13B):c.263G>A (p.Ser88Asn) rs759002769
NM_012452.3(TNFRSF13B):c.288C>T (p.His96=) rs778997868
NM_012452.3(TNFRSF13B):c.304T>C (p.Tyr102His) rs767933010
NM_012452.3(TNFRSF13B):c.309C>G (p.Phe103Leu)
NM_012452.3(TNFRSF13B):c.317A>G (p.Asn106Ser) rs2087567988
NM_012452.3(TNFRSF13B):c.350_356del (p.Glu117fs) rs1293048695
NM_012452.3(TNFRSF13B):c.391G>A (p.Asp131Asn)
NM_012452.3(TNFRSF13B):c.395A>G (p.Asn132Ser)
NM_012452.3(TNFRSF13B):c.3G>T (p.Met1Ile) rs772864862
NM_012452.3(TNFRSF13B):c.40C>G (p.Arg14Gly)
NM_012452.3(TNFRSF13B):c.41G>T (p.Arg14Leu) rs200309474
NM_012452.3(TNFRSF13B):c.425G>C (p.Arg142Thr)
NM_012452.3(TNFRSF13B):c.428G>A (p.Gly143Asp)
NM_012452.3(TNFRSF13B):c.431C>T (p.Ser144Leu) rs104894650
NM_012452.3(TNFRSF13B):c.433G>A (p.Glu145Lys)
NM_012452.3(TNFRSF13B):c.437C>T (p.Ala146Val)
NM_012452.3(TNFRSF13B):c.445+4A>C rs2087566426
NM_012452.3(TNFRSF13B):c.446-3C>A
NM_012452.3(TNFRSF13B):c.446-5T>C rs769761979
NM_012452.3(TNFRSF13B):c.472G>A (p.Asp158Asn) rs1206383760
NM_012452.3(TNFRSF13B):c.476A>T (p.Gln159Leu) rs2143642404
NM_012452.3(TNFRSF13B):c.477G>C (p.Gln159His) rs2087502189
NM_012452.3(TNFRSF13B):c.481G>A (p.Ala161Thr) rs2087502124
NM_012452.3(TNFRSF13B):c.493A>G (p.Ser165Gly)
NM_012452.3(TNFRSF13B):c.532T>C (p.Phe178Leu) rs764319738
NM_012452.3(TNFRSF13B):c.53A>G (p.Glu18Gly) rs1597672265
NM_012452.3(TNFRSF13B):c.542C>T (p.Ala181Val)
NM_012452.3(TNFRSF13B):c.548C>G (p.Ala183Gly)
NM_012452.3(TNFRSF13B):c.55G>A (p.Glu19Lys)
NM_012452.3(TNFRSF13B):c.561G>C (p.Lys187Asn)
NM_012452.3(TNFRSF13B):c.565A>G (p.Arg189Gly) rs2087500977
NM_012452.3(TNFRSF13B):c.566G>A (p.Arg189Lys) rs199777698
NM_012452.3(TNFRSF13B):c.567_568delinsTT (p.Arg189_Gly190delinsSerTrp) rs1597656815
NM_012452.3(TNFRSF13B):c.568G>A (p.Gly190Arg) rs150101848
NM_012452.3(TNFRSF13B):c.571G>A (p.Asp191Asn) rs753867822
NM_012452.3(TNFRSF13B):c.571G>C (p.Asp191His)
NM_012452.3(TNFRSF13B):c.571del (p.Asp191fs)
NM_012452.3(TNFRSF13B):c.587_598del (p.Gln196_Ser199del) rs2087500281
NM_012452.3(TNFRSF13B):c.5G>A (p.Ser2Asn) rs2087749412
NM_012452.3(TNFRSF13B):c.60C>G (p.Arg20=) rs2143696693
NM_012452.3(TNFRSF13B):c.631+8C>T rs1210149250
NM_012452.3(TNFRSF13B):c.631G>A (p.Asp211Asn)
NM_012452.3(TNFRSF13B):c.635A>C (p.His212Pro)
NM_012452.3(TNFRSF13B):c.662G>A (p.Ser221Asn) rs1201167195
NM_012452.3(TNFRSF13B):c.667T>A (p.Ser223Thr)
NM_012452.3(TNFRSF13B):c.674A>G (p.Glu225Gly) rs2087494088
NM_012452.3(TNFRSF13B):c.677C>G (p.Pro226Arg)
NM_012452.3(TNFRSF13B):c.689G>A (p.Cys230Tyr) rs1457538261
NM_012452.3(TNFRSF13B):c.722C>A (p.Thr241Lys)
NM_012452.3(TNFRSF13B):c.732C>G (p.Ser244Arg)
NM_012452.3(TNFRSF13B):c.733G>A (p.Ala245Thr)
NM_012452.3(TNFRSF13B):c.745G>C (p.Gly249Arg) rs2143640077
NM_012452.3(TNFRSF13B):c.751C>T (p.Pro251Ser)
NM_012452.3(TNFRSF13B):c.753del (p.Asp252fs) rs755752100
NM_012452.3(TNFRSF13B):c.764G>A (p.Cys255Tyr)
NM_012452.3(TNFRSF13B):c.777G>A (p.Trp259Ter) rs1473965551
NM_012452.3(TNFRSF13B):c.778G>A (p.Gly260Arg)
NM_012452.3(TNFRSF13B):c.788C>T (p.Thr263Ile) rs986325158
NM_012452.3(TNFRSF13B):c.811T>C (p.Cys271Arg)
NM_012452.3(TNFRSF13B):c.840del (p.Ile281fs)
NM_012452.3(TNFRSF13B):c.842T>C (p.Ile281Thr)
NM_012452.3(TNFRSF13B):c.842_857del (p.Ile281fs) rs2087491615
NM_012452.3(TNFRSF13B):c.856G>A (p.Ala286Thr)
NM_012452.3(TNFRSF13B):c.857C>A (p.Ala286Asp) rs886052652
NM_012452.3(TNFRSF13B):c.857C>T (p.Ala286Val) rs886052652
NM_012452.3(TNFRSF13B):c.865G>A (p.Gly289Arg)
NM_012452.3(TNFRSF13B):c.869G>T (p.Gly290Val)
NM_012452.3(TNFRSF13B):c.872del (p.Pro291fs)
NM_012452.3(TNFRSF13B):c.91A>G (p.Met31Val)
NM_012452.3(TNFRSF13B):c.96A>T (p.Arg32Ser)

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