ClinVar Miner

List of variants in gene TNFRSF13C studied for immune system disorder

Included ClinVar conditions (908):
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Gene type:
ClinVar version:
Total variants: 49
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HGVS dbSNP gnomAD frequency
NM_052945.4(TNFRSF13C):c.*120T>C rs7290134 0.41881
NM_052945.4(TNFRSF13C):c.475C>T (p.His159Tyr) rs61756766 0.00573
NM_052945.4(TNFRSF13C):c.367+18G>A rs200206184 0.00114
NM_052945.4(TNFRSF13C):c.368-15C>A rs372331667 0.00073
NM_052945.4(TNFRSF13C):c.436C>T (p.Pro146Ser) rs151243201 0.00073
NM_052945.4(TNFRSF13C):c.375G>A (p.Glu125=) rs371805226 0.00017
NM_052945.4(TNFRSF13C):c.405G>A (p.Pro135=) rs140406834 0.00008
NM_052945.4(TNFRSF13C):c.*113G>A rs550105406 0.00004
NM_052945.4(TNFRSF13C):c.424G>A (p.Ala142Thr) rs367567995 0.00002
NM_052945.4(TNFRSF13C):c.347C>T (p.Ala116Val) rs886057588 0.00001
NM_052945.4(TNFRSF13C):c.360C>T (p.Asp120=) rs756643677 0.00001
NM_052945.4(TNFRSF13C):c.367+14G>C rs781263826 0.00001
NM_052945.4(TNFRSF13C):c.367+16A>G rs755181593 0.00001
NM_052945.4(TNFRSF13C):c.367G>A (p.Ala123Thr) rs1303897969 0.00001
NM_052945.4(TNFRSF13C):c.368-10C>G rs374836008 0.00001
NM_052945.4(TNFRSF13C):c.392T>C (p.Ile131Thr) rs1013387691 0.00001
NM_052945.4(TNFRSF13C):c.433T>A (p.Trp145Arg) rs1180513439 0.00001
NM_052945.4(TNFRSF13C):c.447G>A (p.Gly149=) rs746050423 0.00001
NM_052945.4(TNFRSF13C):c.538G>A (p.Gly180Ser) rs772090919 0.00001
NC_000022.11:g.(?_41925347)_(41926793_?)dup
NM_052945.4(TNFRSF13C):c.*107G>C rs2077623255
NM_052945.4(TNFRSF13C):c.*253C>T rs2077622673
NM_052945.4(TNFRSF13C):c.344A>T (p.Glu115Val) rs2077628213
NM_052945.4(TNFRSF13C):c.351C>G (p.Pro117=) rs577781803
NM_052945.4(TNFRSF13C):c.357A>G (p.Gly119=)
NM_052945.4(TNFRSF13C):c.367+10G>T rs1052448266
NM_052945.4(TNFRSF13C):c.367+1del
NM_052945.4(TNFRSF13C):c.368-13C>G rs201892760
NM_052945.4(TNFRSF13C):c.368-13C>T rs201892760
NM_052945.4(TNFRSF13C):c.370C>T (p.Pro124Ser)
NM_052945.4(TNFRSF13C):c.375G>T (p.Glu125Asp)
NM_052945.4(TNFRSF13C):c.403C>T (p.Pro135Ser) rs1385697615
NM_052945.4(TNFRSF13C):c.431C>T (p.Ala144Val) rs1000961266
NM_052945.4(TNFRSF13C):c.445G>A (p.Gly149Arg)
NM_052945.4(TNFRSF13C):c.452A>T (p.Asp151Val) rs942451212
NM_052945.4(TNFRSF13C):c.478A>G (p.Ser160Gly) rs1569421592
NM_052945.4(TNFRSF13C):c.479G>T (p.Ser160Ile) rs2146588362
NM_052945.4(TNFRSF13C):c.485C>T (p.Pro162Leu) rs1602373110
NM_052945.4(TNFRSF13C):c.497C>T (p.Thr166Ile) rs1185675031
NM_052945.4(TNFRSF13C):c.504G>A (p.Leu168=)
NM_052945.4(TNFRSF13C):c.507C>T (p.Gly169=) rs1200767252
NM_052945.4(TNFRSF13C):c.508T>C (p.Ser170Pro)
NM_052945.4(TNFRSF13C):c.511A>T (p.Thr171Ser)
NM_052945.4(TNFRSF13C):c.512C>G (p.Thr171Ser)
NM_052945.4(TNFRSF13C):c.522G>A (p.Val174=)
NM_052945.4(TNFRSF13C):c.534_543delinsAATAGCAGG (p.Ala179fs) rs1602373048
NM_052945.4(TNFRSF13C):c.537C>G (p.Ala179=) rs146580897
NM_052945.4(TNFRSF13C):c.537C>T (p.Ala179=) rs146580897
NM_052945.4(TNFRSF13C):c.538G>C (p.Gly180Arg)

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