ClinVar Miner

List of variants in gene TNFRSF11B studied for bone Paget disease

Included ClinVar conditions (10):
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Gene type:
ClinVar version:
Total variants: 64
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HGVS dbSNP gnomAD frequency
NM_002546.4(TNFRSF11B):c.401-5T>C rs3134046 0.93049
NM_002546.4(TNFRSF11B):c.9C>G (p.Asn3Lys) rs2073618 0.60108
NM_002546.3(TNFRSF11B):c.-223C>T rs2073617 0.57443
NM_002546.4(TNFRSF11B):c.768A>G (p.Leu256=) rs2228568 0.09806
NM_002546.4(TNFRSF11B):c.400+4C>T rs1564858 0.09777
NM_002546.4(TNFRSF11B):c.817+8A>C rs7844539 0.09748
NM_002546.4(TNFRSF11B):c.30+15C>T rs3102734 0.09631
NM_002546.4(TNFRSF11B):c.*367G>A rs7815884 0.08889
NM_002546.4(TNFRSF11B):c.1150T>C (p.Leu384=) rs1804854 0.08839
NM_002546.4(TNFRSF11B):c.31-7C>T rs10505344 0.05640
NM_002546.4(TNFRSF11B):c.*583T>A rs7815440 0.03482
NM_002546.4(TNFRSF11B):c.714G>A (p.Glu238=) rs11573930 0.02453
NM_002546.4(TNFRSF11B):c.*545T>C rs11573947 0.00754
NM_002546.4(TNFRSF11B):c.558C>T (p.Ser186=) rs11573923 0.00484
NM_002546.3(TNFRSF11B):c.-284C>T rs11575929 0.00457
NM_002546.4(TNFRSF11B):c.885T>A (p.Leu295=) rs11573942 0.00387
NM_002546.4(TNFRSF11B):c.*67C>T rs11573944 0.00356
NM_002546.3(TNFRSF11B):c.-257G>T rs368831724 0.00255
NM_002546.4(TNFRSF11B):c.*682T>C rs189721016 0.00227
NM_002546.4(TNFRSF11B):c.234C>T (p.Asp78=) rs144654126 0.00081
NM_002546.4(TNFRSF11B):c.841G>A (p.Val281Met) rs140782326 0.00076
NM_002546.4(TNFRSF11B):c.*609G>A rs529941362 0.00052
NM_002546.4(TNFRSF11B):c.700G>A (p.Ala234Thr) rs201393730 0.00047
NM_002546.4(TNFRSF11B):c.96C>T (p.Asp32=) rs4876870 0.00022
NM_002546.4(TNFRSF11B):c.310G>A (p.Val104Met) rs11573906 0.00021
NM_002546.4(TNFRSF11B):c.840C>T (p.Ser280=) rs143414212 0.00021
NM_002546.4(TNFRSF11B):c.104C>A (p.Thr35Asn) rs150777320 0.00014
NM_002546.4(TNFRSF11B):c.21C>T (p.Cys7=) rs373330021 0.00014
NM_002546.4(TNFRSF11B):c.332G>A (p.Arg111His) rs200629343 0.00009
NM_002546.4(TNFRSF11B):c.853A>G (p.Ile285Val) rs373848556 0.00009
NM_002546.3(TNFRSF11B):c.-311G>T rs779000439 0.00008
NM_002546.4(TNFRSF11B):c.621C>T (p.Phe207=) rs376708982 0.00008
NM_002546.4(TNFRSF11B):c.277G>A (p.Val93Ile) rs369646136 0.00007
NM_002546.4(TNFRSF11B):c.729A>T (p.Gln243His) rs374594601 0.00006
NM_002546.4(TNFRSF11B):c.*213C>T rs569762226 0.00004
NM_002546.4(TNFRSF11B):c.*349T>A rs888097904 0.00004
NM_002546.4(TNFRSF11B):c.-10G>A rs752426445 0.00004
NM_002546.4(TNFRSF11B):c.308G>A (p.Arg103His) rs375274060 0.00004
NM_002546.4(TNFRSF11B):c.349T>C (p.Phe117Leu) rs104894092 0.00003
NM_002546.4(TNFRSF11B):c.400+5G>A rs372860364 0.00003
NM_002546.4(TNFRSF11B):c.400+15G>A rs757467378 0.00002
NM_002546.3(TNFRSF11B):c.-191C>G rs886062648 0.00001
NM_002546.3(TNFRSF11B):c.-99G>A rs886062647 0.00001
NM_002546.4(TNFRSF11B):c.*487T>C rs1421622252 0.00001
NM_002546.4(TNFRSF11B):c.*505A>G rs1812213517 0.00001
NM_002546.4(TNFRSF11B):c.*799G>A rs1397220907 0.00001
NM_002546.4(TNFRSF11B):c.720A>G (p.Ile240Met) rs767927201 0.00001
NM_002546.4(TNFRSF11B):c.997C>T (p.Arg333Ter) rs1307942060 0.00001
NM_002546.3(TNFRSF11B):c.-204C>T rs570347828
NM_002546.3(TNFRSF11B):c.-215C>T rs886062649
NM_002546.4(TNFRSF11B):c.*166C>G rs1812218708
NM_002546.4(TNFRSF11B):c.*207C>G rs886062646
NM_002546.4(TNFRSF11B):c.*412A>G rs1379870216
NM_002546.4(TNFRSF11B):c.*463T>A rs574050965
NM_002546.4(TNFRSF11B):c.139G>A (p.Gly47Ser) rs1812353362
NM_002546.4(TNFRSF11B):c.226A>C (p.Thr76Pro) rs200071478
NM_002546.4(TNFRSF11B):c.260G>A (p.Cys87Tyr) rs104894091
NM_002546.4(TNFRSF11B):c.419_420del (p.Thr140fs)
NM_002546.4(TNFRSF11B):c.544_546del (p.Asp182del) rs796051868
NM_002546.4(TNFRSF11B):c.699C>A (p.Asn233Lys) rs150457771
NM_002546.4(TNFRSF11B):c.841G>T (p.Val281Leu) rs140782326
NM_002546.4(TNFRSF11B):c.884T>C (p.Leu295Pro) rs1586952570
NM_002546.4(TNFRSF11B):c.966_969delinsCTT (p.Asp323fs) rs2129878039
NM_002546.4(TNFRSF11B):c.97G>A (p.Glu33Lys) rs202090603

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