ClinVar Miner

List of variants in gene CD4 studied for not specified

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Total variants: 22
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HGVS dbSNP gnomAD frequency
NM_000616.5(CD4):c.*91C>A rs7136817 0.99999
NM_000616.5(CD4):c.*92A>G rs7307451 0.99999
NM_000616.5(CD4):c.49+35A>G rs2365568 0.94173
NM_000616.5(CD4):c.1341T>C (p.Cys447=) rs12821756 0.65245
NM_000616.5(CD4):c.1023T>C (p.Ser341=) rs1055141 0.63742
NM_000616.5(CD4):c.50-31T>C rs2255301 0.61362
NM_000616.5(CD4):c.49+28del rs3216776 0.56473
NM_000616.5(CD4):c.1157-117C>T rs12226953 0.47083
NM_000616.5(CD4):c.608-73C>T rs10744715 0.28847
NM_000616.5(CD4):c.793C>T (p.Arg265Trp) rs28919570 0.06389
NM_000616.5(CD4):c.1330A>G (p.Thr444Ala) rs145973129 0.00019
NM_000616.5(CD4):c.1219G>A (p.Gly407Ser) rs782745228 0.00002
NM_000616.5(CD4):c.1082T>C (p.Leu361Pro) rs1555118104 0.00001
NM_000616.5(CD4):c.982T>C (p.Cys328Arg) rs1366978901 0.00001
NM_000616.5(CD4):c.1055C>G (p.Ser352Trp) rs201791740
NM_000616.5(CD4):c.1183C>A (p.Gln395Lys) rs2542289591
NM_000616.5(CD4):c.1202T>C (p.Val401Ala)
NM_000616.5(CD4):c.1347C>T (p.His449=) rs2542294674
NM_000616.5(CD4):c.1348C>T (p.Arg450Trp) rs782208003
NM_000616.5(CD4):c.369C>A (p.Phe123Leu) rs11064416
NM_000616.5(CD4):c.557T>C (p.Val186Ala) rs2542272271
NM_000616.5(CD4):c.676G>A (p.Ala226Thr) rs150742570

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