ClinVar Miner

List of variants in gene TNFRSF13B studied for agammaglobulinemia

Included ClinVar conditions (31):
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Gene type:
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Total variants: 66
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HGVS dbSNP
NM_012452.2(TNFRSF13B):c.*86_*88delTGA rs150068036
NM_012452.2(TNFRSF13B):c.145T>C (p.Ser49Pro) rs374547688
NM_012452.2(TNFRSF13B):c.165C>T (p.Asn55=) rs756655390
NM_012452.2(TNFRSF13B):c.178C>T (p.Arg60Cys)
NM_012452.2(TNFRSF13B):c.17G>A (p.Arg6Gln) rs747078163
NM_012452.2(TNFRSF13B):c.204dup (p.Leu69fs) rs72553875
NM_012452.2(TNFRSF13B):c.215G>A (p.Arg72His) rs55916807
NM_012452.2(TNFRSF13B):c.21C>T (p.Ser7=)
NM_012452.2(TNFRSF13B):c.222_226GCAAG[1] (p.Gly76fs)
NM_012452.2(TNFRSF13B):c.227G>A (p.Gly76Asp)
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.291T>G (p.Pro97=) rs35062843
NM_012452.2(TNFRSF13B):c.310T>C (p.Cys104Arg) rs34557412
NM_012452.2(TNFRSF13B):c.311G>A (p.Cys104Tyr)
NM_012452.2(TNFRSF13B):c.346C>A (p.Pro116Thr)
NM_012452.2(TNFRSF13B):c.364C>T (p.Arg122Trp)
NM_012452.2(TNFRSF13B):c.431C>A (p.Ser144Ter) rs104894650
NM_012452.2(TNFRSF13B):c.431C>G (p.Ser144Ter) rs104894650
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)
NM_012452.2(TNFRSF13B):c.492C>G (p.Tyr164Ter) rs72553882
NM_012452.2(TNFRSF13B):c.49del (p.Gln17fs) rs1555550717
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.519C>T (p.Ala173=) rs151139237
NM_012452.2(TNFRSF13B):c.532T>C (p.Phe178Leu) rs764319738
NM_012452.2(TNFRSF13B):c.542C>A (p.Ala181Glu) rs72553883
NM_012452.2(TNFRSF13B):c.543G>A (p.Ala181=)
NM_012452.2(TNFRSF13B):c.560_562AGA[1] (p.Lys188del) rs376630110
NM_012452.2(TNFRSF13B):c.563A>T (p.Lys188Met) rs74811083
NM_012452.2(TNFRSF13B):c.566G>T (p.Arg189Met) rs199777698
NM_012452.2(TNFRSF13B):c.567G>C (p.Arg189Ser)
NM_012452.2(TNFRSF13B):c.567_568delinsTT (p.Arg189_Gly190delinsSerTrp)
NM_012452.2(TNFRSF13B):c.568G>A (p.Gly190Arg)
NM_012452.2(TNFRSF13B):c.572dup (p.Asp191fs) rs769165409
NM_012452.2(TNFRSF13B):c.577T>C (p.Cys193Arg) rs764125338
NM_012452.2(TNFRSF13B):c.579C>A (p.Cys193Ter)
NM_012452.2(TNFRSF13B):c.581_582delCCinsAA (p.Ser194Ter) rs121908379
NM_012452.2(TNFRSF13B):c.58C>T (p.Arg20Cys)
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.605G>A (p.Arg202His) rs104894649
NM_012452.2(TNFRSF13B):c.61+10C>T rs148297590
NM_012452.2(TNFRSF13B):c.61+1G>T
NM_012452.2(TNFRSF13B):c.631+8C>T rs1210149250
NM_012452.2(TNFRSF13B):c.638C>T (p.Ala213Val)
NM_012452.2(TNFRSF13B):c.641T>C (p.Met214Thr) rs144560464
NM_012452.2(TNFRSF13B):c.659T>C (p.Val220Ala) rs56063729
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)
NM_012452.2(TNFRSF13B):c.740C>T (p.Thr247Met)
NM_012452.2(TNFRSF13B):c.754G>A (p.Asp252Asn) rs111439115
NM_012452.2(TNFRSF13B):c.76T>C (p.Trp26Arg)
NM_012452.2(TNFRSF13B):c.776G>A (p.Trp259Ter)
NM_012452.2(TNFRSF13B):c.797C>T (p.Thr266Ile) rs752825527
NM_012452.2(TNFRSF13B):c.81G>A (p.Thr27=) rs8072293
NM_012452.2(TNFRSF13B):c.823C>T (p.Pro275Ser)
NM_012452.2(TNFRSF13B):c.828C>G (p.Asp276Glu) rs144383122
NM_012452.2(TNFRSF13B):c.838G>C (p.Gly280Arg)
NM_012452.2(TNFRSF13B):c.857C>T (p.Ala286Val)
NM_012452.2(TNFRSF13B):c.93_94GA[3] (p.Ser33fs)
TNFRSF13B, 1-BP INS, 204A

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