ClinVar Miner

List of variants in gene TNFRSF13B reported as uncertain significance by CeGaT Center for Human Genetics Tuebingen

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Gene type:
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Total variants: 18
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HGVS dbSNP gnomAD frequency
NM_012452.3(TNFRSF13B):c.605G>A (p.Arg202His) rs104894649 0.00076
NM_012452.3(TNFRSF13B):c.260T>A (p.Ile87Asn) rs72553877 0.00034
NM_012452.3(TNFRSF13B):c.515G>A (p.Cys172Tyr) rs751216929 0.00020
NM_012452.3(TNFRSF13B):c.171G>C (p.Gln57His) rs149084717 0.00018
NM_012452.3(TNFRSF13B):c.512T>G (p.Leu171Arg) rs143027621 0.00012
NM_012452.3(TNFRSF13B):c.58C>T (p.Arg20Cys) rs200013015 0.00012
NM_012452.3(TNFRSF13B):c.706G>T (p.Glu236Ter) rs201021960 0.00010
NM_012452.3(TNFRSF13B):c.577T>C (p.Cys193Arg) rs764125338 0.00009
NM_012452.3(TNFRSF13B):c.445+7C>T rs768915966 0.00008
NM_012452.3(TNFRSF13B):c.452C>T (p.Pro151Leu) rs200037919 0.00006
NM_012452.3(TNFRSF13B):c.779G>A (p.Gly260Glu) rs150660451 0.00006
NM_012452.3(TNFRSF13B):c.214C>T (p.Arg72Cys) rs375514495 0.00004
NM_012452.3(TNFRSF13B):c.693C>G (p.Ser231Arg) rs145711865 0.00003
NM_012452.3(TNFRSF13B):c.266G>A (p.Cys89Tyr) rs746779126 0.00001
NM_012452.3(TNFRSF13B):c.290C>G (p.Pro97Arg) rs754139414 0.00001
NM_012452.3(TNFRSF13B):c.529T>C (p.Cys177Arg) rs761877520 0.00001
NM_012452.3(TNFRSF13B):c.554T>G (p.Phe185Cys) rs778227535 0.00001
NM_012452.3(TNFRSF13B):c.257G>C (p.Cys86Ser) rs1597661284

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