ClinVar Miner

List of variants in gene TNFRSF13B reported as likely benign for Immunodeficiency, common variable, 2

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Gene type:
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Total variants: 86
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HGVS dbSNP gnomAD frequency
NM_012452.3(TNFRSF13B):c.659T>C (p.Val220Ala) rs56063729 0.01586
NM_012452.3(TNFRSF13B):c.215G>A (p.Arg72His) rs55916807 0.00261
NM_012452.3(TNFRSF13B):c.568G>C (p.Gly190Arg) rs150101848 0.00083
NM_012452.3(TNFRSF13B):c.519C>T (p.Ala173=) rs151139237 0.00061
NM_012452.3(TNFRSF13B):c.446-19G>T rs751183621 0.00015
NM_012452.3(TNFRSF13B):c.445+7C>T rs768915966 0.00008
NM_012452.3(TNFRSF13B):c.561G>A (p.Lys187=) rs373469090 0.00008
NM_012452.3(TNFRSF13B):c.593G>A (p.Arg198His) rs150974807 0.00006
NM_012452.3(TNFRSF13B):c.105C>T (p.Pro35=) rs200868537 0.00005
NM_012452.3(TNFRSF13B):c.543G>A (p.Ala181=) rs746018705 0.00005
NM_012452.3(TNFRSF13B):c.531C>T (p.Cys177=) rs34088818 0.00004
NM_012452.3(TNFRSF13B):c.632-10G>A rs748883051 0.00004
NM_012452.3(TNFRSF13B):c.774G>A (p.Arg258=) rs757425278 0.00004
NM_012452.3(TNFRSF13B):c.446-6T>C rs773058896 0.00003
NM_012452.3(TNFRSF13B):c.648C>T (p.Ala216=) rs777265646 0.00003
NM_012452.3(TNFRSF13B):c.717G>A (p.Ala239=) rs199603343 0.00003
NM_012452.3(TNFRSF13B):c.231G>A (p.Lys77=) rs371317735 0.00002
NM_012452.3(TNFRSF13B):c.446-20G>A rs759191629 0.00002
NM_012452.3(TNFRSF13B):c.631+10T>C rs367988346 0.00002
NM_012452.3(TNFRSF13B):c.690C>T (p.Cys230=) rs746878754 0.00002
NM_012452.3(TNFRSF13B):c.75G>A (p.Leu25=) rs749666239 0.00002
NM_012452.3(TNFRSF13B):c.165C>T (p.Asn55=) rs756655390 0.00001
NM_012452.3(TNFRSF13B):c.200-4C>G rs779828195 0.00001
NM_012452.3(TNFRSF13B):c.327G>A (p.Arg109=) rs746618447 0.00001
NM_012452.3(TNFRSF13B):c.399G>A (p.Ser133=) rs371292644 0.00001
NM_012452.3(TNFRSF13B):c.62-9G>A rs1325092488 0.00001
NM_012452.3(TNFRSF13B):c.633T>C (p.Asp211=) rs199592890 0.00001
NM_012452.3(TNFRSF13B):c.639G>A (p.Ala213=) rs750598581 0.00001
NM_012452.3(TNFRSF13B):c.672C>T (p.Pro224=) rs769670646 0.00001
NM_012452.3(TNFRSF13B):c.102C>T (p.Cys34=)
NM_012452.3(TNFRSF13B):c.18G>C (p.Arg6=)
NM_012452.3(TNFRSF13B):c.199+15C>T
NM_012452.3(TNFRSF13B):c.199+8C>T
NM_012452.3(TNFRSF13B):c.200-16A>C rs2087569971
NM_012452.3(TNFRSF13B):c.200-7C>A
NM_012452.3(TNFRSF13B):c.200-7C>G rs1229410555
NM_012452.3(TNFRSF13B):c.201G>A (p.Arg67=)
NM_012452.3(TNFRSF13B):c.207C>A (p.Leu69=) rs765245909
NM_012452.3(TNFRSF13B):c.226G>A (p.Gly76Ser) rs146436713
NM_012452.3(TNFRSF13B):c.252G>A (p.Arg84=)
NM_012452.3(TNFRSF13B):c.303A>C (p.Ala101=)
NM_012452.3(TNFRSF13B):c.303A>T (p.Ala101=)
NM_012452.3(TNFRSF13B):c.318C>T (p.Asn106=) rs2143656561
NM_012452.3(TNFRSF13B):c.354C>G (p.Leu118=)
NM_012452.3(TNFRSF13B):c.357G>A (p.Arg119=)
NM_012452.3(TNFRSF13B):c.36G>C (p.Arg12=)
NM_012452.3(TNFRSF13B):c.384C>T (p.Asn128=)
NM_012452.3(TNFRSF13B):c.393C>T (p.Asp131=)
NM_012452.3(TNFRSF13B):c.42T>C (p.Arg14=)
NM_012452.3(TNFRSF13B):c.445+10C>T
NM_012452.3(TNFRSF13B):c.453G>A (p.Pro151=)
NM_012452.3(TNFRSF13B):c.465G>A (p.Leu155=) rs2143642450
NM_012452.3(TNFRSF13B):c.484C>T (p.Leu162=) rs2087502054
NM_012452.3(TNFRSF13B):c.489C>A (p.Val163=) rs2143642351
NM_012452.3(TNFRSF13B):c.498G>A (p.Thr166=)
NM_012452.3(TNFRSF13B):c.513G>A (p.Leu171=)
NM_012452.3(TNFRSF13B):c.555C>T (p.Phe185=)
NM_012452.3(TNFRSF13B):c.567G>A (p.Arg189=) rs370856157
NM_012452.3(TNFRSF13B):c.61+10_61+11del
NM_012452.3(TNFRSF13B):c.61+11G>A rs201483236
NM_012452.3(TNFRSF13B):c.61+11G>C rs201483236
NM_012452.3(TNFRSF13B):c.61+16G>A
NM_012452.3(TNFRSF13B):c.61+7A>C
NM_012452.3(TNFRSF13B):c.615G>A (p.Pro205=)
NM_012452.3(TNFRSF13B):c.62-11T>C
NM_012452.3(TNFRSF13B):c.632-11C>T rs375314767
NM_012452.3(TNFRSF13B):c.632-13C>A
NM_012452.3(TNFRSF13B):c.632-13C>T
NM_012452.3(TNFRSF13B):c.632-5T>C
NM_012452.3(TNFRSF13B):c.663C>T (p.Ser221=) rs533796529
NM_012452.3(TNFRSF13B):c.684G>A (p.Glu228=)
NM_012452.3(TNFRSF13B):c.702C>T (p.Phe234=)
NM_012452.3(TNFRSF13B):c.705T>C (p.Pro235=)
NM_012452.3(TNFRSF13B):c.723G>A (p.Thr241=) rs766034334
NM_012452.3(TNFRSF13B):c.723G>T (p.Thr241=) rs766034334
NM_012452.3(TNFRSF13B):c.72C>A (p.Gly24=)
NM_012452.3(TNFRSF13B):c.732C>T (p.Ser244=)
NM_012452.3(TNFRSF13B):c.73C>T (p.Leu25=) rs1166959410
NM_012452.3(TNFRSF13B):c.744T>G (p.Pro248=) rs2143640084
NM_012452.3(TNFRSF13B):c.753C>T (p.Pro251=)
NM_012452.3(TNFRSF13B):c.765T>C (p.Cys255=) rs2143640004
NM_012452.3(TNFRSF13B):c.780G>A (p.Gly260=) rs922685521
NM_012452.3(TNFRSF13B):c.813C>T (p.Cys271=)
NM_012452.3(TNFRSF13B):c.843T>C (p.Ile281=) rs1597656219
NM_012452.3(TNFRSF13B):c.870C>A (p.Gly290=) rs2087491333
NM_012452.3(TNFRSF13B):c.870C>T (p.Gly290=) rs2087491333

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