ClinVar Miner

List of variants reported as uncertain significance for Common variable immunodeficiency 2

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Total variants: 53
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HGVS dbSNP
NM_012452.2(TNFRSF13B):c.*86_*88del rs150068036
NM_012452.2(TNFRSF13B):c.145T>C (p.Ser49Pro) rs374547688
NM_012452.2(TNFRSF13B):c.178C>T (p.Arg60Cys) rs777555444
NM_012452.2(TNFRSF13B):c.17G>A (p.Arg6Gln) rs747078163
NM_012452.2(TNFRSF13B):c.21C>T (p.Ser7=) rs780461208
NM_012452.2(TNFRSF13B):c.227G>A (p.Gly76Asp) rs772701872
NM_012452.2(TNFRSF13B):c.236A>G (p.Tyr79Cys) rs72553876
NM_012452.2(TNFRSF13B):c.260T>A (p.Ile87Asn) rs72553877
NM_012452.2(TNFRSF13B):c.290C>G (p.Pro97Arg) rs754139414
NM_012452.2(TNFRSF13B):c.346C>A (p.Pro116Thr) rs757399024
NM_012452.2(TNFRSF13B):c.364C>T (p.Arg122Trp) rs201124889
NM_012452.2(TNFRSF13B):c.452C>T (p.Pro151Leu) rs200037919
NM_012452.2(TNFRSF13B):c.453G>C (p.Pro151=) rs768819413
NM_012452.2(TNFRSF13B):c.468T>G (p.Ser156Arg) rs148758686
NM_012452.2(TNFRSF13B):c.512T>G (p.Leu171Arg) rs143027621
NM_012452.2(TNFRSF13B):c.515G>A (p.Cys172Tyr) rs751216929
NM_012452.2(TNFRSF13B):c.532T>C (p.Phe178Leu) rs764319738
NM_012452.2(TNFRSF13B):c.543G>A (p.Ala181=) rs746018705
NM_012452.2(TNFRSF13B):c.566G>T (p.Arg189Met) rs199777698
NM_012452.2(TNFRSF13B):c.567G>C (p.Arg189Ser) rs370856157
NM_012452.2(TNFRSF13B):c.567_568delinsTT (p.Arg189_Gly190delinsSerTrp) rs1597656815
NM_012452.2(TNFRSF13B):c.568G>A (p.Gly190Arg) rs150101848
NM_012452.2(TNFRSF13B):c.577T>C (p.Cys193Arg) rs764125338
NM_012452.2(TNFRSF13B):c.58C>T (p.Arg20Cys) rs200013015
NM_012452.2(TNFRSF13B):c.592C>T (p.Arg198Cys) rs140781824
NM_012452.2(TNFRSF13B):c.604C>T (p.Arg202Cys) rs143562358
NM_012452.2(TNFRSF13B):c.631+8C>T rs1210149250
NM_012452.2(TNFRSF13B):c.638C>T (p.Ala213Val) rs763164041
NM_012452.2(TNFRSF13B):c.641T>C (p.Met214Thr) rs144560464
NM_012452.2(TNFRSF13B):c.706G>T (p.Glu236Ter) rs201021960
NM_012452.2(TNFRSF13B):c.716C>T (p.Ala239Val) rs375891337
NM_012452.2(TNFRSF13B):c.722C>T (p.Thr241Met) rs370250196
NM_012452.2(TNFRSF13B):c.740C>T (p.Thr247Met) rs149635611
NM_012452.2(TNFRSF13B):c.754G>A (p.Asp252Asn) rs111439115
NM_012452.2(TNFRSF13B):c.76T>C (p.Trp26Arg) rs773591883
NM_012452.2(TNFRSF13B):c.776G>A (p.Trp259Ter) rs764387835
NM_012452.2(TNFRSF13B):c.797C>T (p.Thr266Ile) rs752825527
NM_012452.2(TNFRSF13B):c.823C>T (p.Pro275Ser) rs540918755
NM_012452.2(TNFRSF13B):c.828C>G (p.Asp276Glu) rs144383122
NM_012452.2(TNFRSF13B):c.838G>C (p.Gly280Arg) rs374957601
NM_012452.2(TNFRSF13B):c.857C>A (p.Ala286Asp) rs886052652
NM_012452.2(TNFRSF13B):c.857C>T (p.Ala286Val) rs886052652
NM_012452.3(TNFRSF13B):c.118T>C (p.Trp40Arg) rs72553874
NM_012452.3(TNFRSF13B):c.16C>T (p.Arg6Trp)
NM_012452.3(TNFRSF13B):c.171G>C (p.Gln57His)
NM_012452.3(TNFRSF13B):c.214C>T (p.Arg72Cys)
NM_012452.3(TNFRSF13B):c.317A>G (p.Asn106Ser)
NM_012452.3(TNFRSF13B):c.365G>A (p.Arg122Gln)
NM_012452.3(TNFRSF13B):c.418G>A (p.Glu140Lys)
NM_012452.3(TNFRSF13B):c.571G>A (p.Asp191Asn)
NM_012452.3(TNFRSF13B):c.61+5G>A
NM_012452.3(TNFRSF13B):c.612T>G (p.Ser204Arg)
NM_012452.3(TNFRSF13B):c.631G>C (p.Asp211His)

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