ClinVar Miner

List of variants reported as benign for Immunodeficiency 51

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Total variants: 51
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HGVS dbSNP gnomAD frequency
NM_014339.7(IL17RA):c.-8G>C rs917865 0.84062
NM_014339.7(IL17RA):c.932-10C>T rs2241046 0.81871
NM_014339.7(IL17RA):c.1100C>T (p.Ala367Val) rs879577 0.29184
NM_014339.7(IL17RA):c.2160C>T (p.Pro720=) rs4819555 0.25992
NM_014339.7(IL17RA):c.1458C>T (p.Ile486=) rs879575 0.20567
NM_014339.7(IL17RA):c.1137G>A (p.Lys379=) rs879576 0.15008
NM_014339.7(IL17RA):c.2071G>A (p.Ala691Thr) rs41323645 0.13701
NM_014339.7(IL17RA):c.*249A>C rs5994164 0.02803
NM_014339.7(IL17RA):c.2295G>A (p.Gln765=) rs41482444 0.02725
NM_014339.7(IL17RA):c.*3060A>G rs12157837 0.02397
NM_014339.7(IL17RA):c.1685C>A (p.Pro562Gln) rs12484684 0.02190
NM_014339.7(IL17RA):c.1188G>A (p.Leu396=) rs2229151 0.02175
NM_014339.7(IL17RA):c.*5256C>T rs1003944 0.01864
NM_014339.7(IL17RA):c.*5270C>T rs1003943 0.01714
NM_014339.7(IL17RA):c.*5659G>A rs7289055 0.01147
NM_014339.7(IL17RA):c.*5036C>T rs1003945 0.01136
NM_014339.7(IL17RA):c.551-9G>T rs17205308 0.00859
NM_014339.7(IL17RA):c.1819G>A (p.Glu607Lys) rs28376631 0.00845
NM_014339.7(IL17RA):c.2490C>T (p.Pro830=) rs3804060 0.00761
NM_014339.7(IL17RA):c.*238G>C rs143922111 0.00671
NM_014339.7(IL17RA):c.*2112C>T rs12159073 0.00663
NM_014339.7(IL17RA):c.*1379A>T rs5992627 0.00655
NM_014339.7(IL17RA):c.*2111C>T rs114684847 0.00510
NM_014339.7(IL17RA):c.1116C>T (p.Pro372=) rs138584265 0.00421
NM_014339.7(IL17RA):c.873C>T (p.Leu291=) rs2228077 0.00411
NM_014339.7(IL17RA):c.1747G>C (p.Asp583His) rs41432148 0.00389
NM_014339.7(IL17RA):c.855C>G (p.Pro285=) rs41339945 0.00245
NM_014339.7(IL17RA):c.1530C>T (p.Asp510=) rs148319877 0.00227
NM_014339.7(IL17RA):c.30T>A (p.Ala10=) rs577217331 0.00204
NM_014339.7(IL17RA):c.1689C>T (p.Gly563=) rs146292661 0.00185
NM_014339.7(IL17RA):c.1407C>T (p.Cys469=) rs41396346 0.00122
NM_014339.7(IL17RA):c.944-16G>A rs201595468 0.00098
NM_014339.7(IL17RA):c.2406G>A (p.Pro802=) rs41356751 0.00078
NM_014339.7(IL17RA):c.833G>A (p.Arg278His) rs141467790 0.00070
NM_014339.7(IL17RA):c.2389A>G (p.Ile797Val) rs74827998 0.00018
NM_014339.7(IL17RA):c.*2163G>C rs543545127 0.00013
NM_014339.7(IL17RA):c.*3976G>A rs576803215 0.00009
NM_014339.7(IL17RA):c.889C>T (p.His297Tyr) rs180787596 0.00006
NM_014339.7(IL17RA):c.*2066G>C rs375958748 0.00005
NM_014339.7(IL17RA):c.*3624G>A rs563135481 0.00005
NM_014339.6(IL17RA):c.-126C>G rs562165706
NM_014339.7(IL17RA):c.*803G>A rs12158721
NM_014339.7(IL17RA):c.-33C>G rs41525344
NM_014339.7(IL17RA):c.1046-10dup rs1348186101
NM_014339.7(IL17RA):c.138+12C>T rs534287611
NM_014339.7(IL17RA):c.163+19TTC[2] rs373435632
NM_014339.7(IL17RA):c.424-12C>T rs531208196
NM_014339.7(IL17RA):c.599-17G>A rs41444249
NM_014339.7(IL17RA):c.762+20C>T rs145541428
NM_014339.7(IL17RA):c.765C>T (p.Pro255=)
NM_014339.7(IL17RA):c.931+7del rs531944007

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