ClinVar Miner

List of variants in gene TNFRSF13C studied for agammaglobulinemia

Included ClinVar conditions (31):
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Gene type:
ClinVar version:
Total variants: 20
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HGVS dbSNP
NM_052945.3(TNFRSF13C):c.122C>T (p.Pro41Leu) rs1556159000
NM_052945.3(TNFRSF13C):c.132A>G (p.Lys44=) rs920471641
NM_052945.3(TNFRSF13C):c.137-7delG rs1299671576
NM_052945.3(TNFRSF13C):c.173A>T (p.Gln58Leu)
NM_052945.3(TNFRSF13C):c.181G>A (p.Glu61Lys) rs1052712048
NM_052945.3(TNFRSF13C):c.191_192delinsTT (p.Gly64Val) rs1556157858
NM_052945.3(TNFRSF13C):c.213G>A (p.Ala71=) rs767759337
NM_052945.3(TNFRSF13C):c.229C>T (p.Leu77=) rs140820836
NM_052945.3(TNFRSF13C):c.264A>G (p.Ala88=) rs778024793
NM_052945.3(TNFRSF13C):c.282C>T (p.Val94=) rs190252814
NM_052945.3(TNFRSF13C):c.317G>A (p.Arg106Gln) rs150374940
NM_052945.3(TNFRSF13C):c.325C>T (p.Arg109Cys)
NM_052945.3(TNFRSF13C):c.367+10G>T rs1052448266
NM_052945.3(TNFRSF13C):c.475C>T (p.His159Tyr) rs61756766
NM_052945.3(TNFRSF13C):c.478A>G (p.Ser160Gly) rs1569421592
NM_052945.3(TNFRSF13C):c.485C>T (p.Pro162Leu)
NM_052945.3(TNFRSF13C):c.534_543delinsAATAGCAGG (p.Ala179fs)
NM_052945.3(TNFRSF13C):c.60C>T (p.Val20=) rs373828157
NM_052945.3(TNFRSF13C):c.62C>G (p.Pro21Arg) rs77874543
TNFRSF13C, 24-BP DEL, NT89

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