ClinVar Miner

List of variants in gene CD40 reported as benign for not provided

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Total variants: 24
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HGVS dbSNP gnomAD frequency
NM_001250.6(CD40):c.676-114G>A rs3765459 0.18322
NM_001250.6(CD40):c.646+28G>A rs3765456 0.11904
NM_001250.6(CD40):c.675+216A>G rs3765457 0.11404
NM_001250.6(CD40):c.131-22C>G rs11569317 0.05959
NM_001250.6(CD40):c.371C>T (p.Ser124Leu) rs11569321 0.04146
NM_001250.6(CD40):c.606C>T (p.Phe202=) rs7273698 0.04009
NM_001250.6(CD40):c.*135C>G rs11569343 0.03655
NM_001250.6(CD40):c.403+20A>G rs11699100 0.02132
NM_001250.6(CD40):c.646+45A>C rs4813000 0.01674
NM_001250.6(CD40):c.*316G>C rs11569344 0.01661
NM_001250.6(CD40):c.679C>G (p.Pro227Ala) rs11086998 0.01507
NM_001250.6(CD40):c.256+109G>A rs11569319 0.01407
NM_001250.6(CD40):c.559+36G>C rs41282788 0.01183
NM_001250.6(CD40):c.52-15C>T rs187683423 0.00235
NM_001250.6(CD40):c.681C>T (p.Pro227=) rs148342289 0.00198
NM_001250.6(CD40):c.717C>T (p.Pro239=) rs144466131 0.00160
NM_001250.6(CD40):c.147T>C (p.Ser49=) rs541686651 0.00004
NM_001250.6(CD40):c.621C>T (p.Ala207=) rs535886332 0.00002
NM_001250.6(CD40):c.498-168G>T rs3746821
NM_001250.6(CD40):c.647-3del rs749590513
NM_001250.6(CD40):c.647-3dup rs749590513
NM_001250.6(CD40):c.647-4_647-3del rs749590513
NM_001250.6(CD40):c.647-4_647-3dup rs749590513
NM_001250.6(CD40):c.675+12del rs2515726938

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