Chr Mutation (hg38) CAid Gene Transcript Linkouts
18g.62358240_62358241insTTTTTTTTTTTTTTTTTTTTGTTTTTTTTTTTTTTTCA920001986TNFRSF11Ac.428-8_428-7insTTTTTTTTTTTTTTTTTTTTGTTTTTTTTTTTTTTT (n.428-8_428-7insTTTTTTTTTTTTTTTTTTTTGTTTTTTTTTTTTTTT)
n.338_339insTTTTTTTTTTTTTTTTTTTTGTTTTTTTTTTTTTTT
c.428-50_428-49insTTTTTTTTTTTTTTTTTTTTGTTTTTTTTTTTTTTT (n.428-50_428-49insTTTTTTTTTTTTTTTTTTTTGTTTTTTTTTTTTTTT)
c.443-8_443-7insTTTTTTTTTTTTTTTTTTTTGTTTTTTTTTTTTTTT (n.443-8_443-7insTTTTTTTTTTTTTTTTTTTTGTTTTTTTTTTTTTTT)
c.325-13_325-12insTTTTTTTTTTTTTTTTTTTTGTTTTTTTTTTTTTTT (n.325-13_325-12insTTTTTTTTTTTTTTTTTTTTGTTTTTTTTTTTTTTT)
n.458-8_458-7insTTTTTTTTTTTTTTTTTTTTGTTTTTTTTTTTTTTT
c.278-8_278-7insTTTTTTTTTTTTTTTTTTTTGTTTTTTTTTTTTTTT (n.278-8_278-7insTTTTTTTTTTTTTTTTTTTTGTTTTTTTTTTTTTTT)
c.223-13_223-12insTTTTTTTTTTTTTTTTTTTTGTTTTTTTTTTTTTTT (n.223-13_223-12insTTTTTTTTTTTTTTTTTTTTGTTTTTTTTTTTTTTT)
 dbSNP
18g.62358240dupCA8983749TNFRSF11Ac.428-8dup (n.428-8dup)
n.338dup
c.428-50dup (n.428-50dup)
c.443-8dup (n.443-8dup)
c.325-13dup (n.325-13dup)
n.458-8dup
c.278-8dup (n.278-8dup)
c.223-13dup (n.223-13dup)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
18g.62358239_62358240dupCA8983750TNFRSF11Ac.428-9_428-8dup (n.428-9_428-8dup)
n.337_338dup
c.428-51_428-50dup (n.428-51_428-50dup)
c.443-9_443-8dup (n.443-9_443-8dup)
c.325-14_325-13dup (n.325-14_325-13dup)
n.458-9_458-8dup
c.278-9_278-8dup (n.278-9_278-8dup)
c.223-14_223-13dup (n.223-14_223-13dup)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
18g.62358238_62358240dupCA8983754TNFRSF11Ac.428-10_428-8dup (n.428-10_428-8dup)
n.336_338dup
c.428-52_428-50dup (n.428-52_428-50dup)
c.443-10_443-8dup (n.443-10_443-8dup)
c.325-15_325-13dup (n.325-15_325-13dup)
n.458-10_458-8dup
c.278-10_278-8dup (n.278-10_278-8dup)
c.223-15_223-13dup (n.223-15_223-13dup)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
18g.62358237_62358240dupCA991036091TNFRSF11Ac.428-11_428-8dup (n.428-11_428-8dup)
n.335_338dup
c.428-53_428-50dup (n.428-53_428-50dup)
c.443-11_443-8dup (n.443-11_443-8dup)
c.325-16_325-13dup (n.325-16_325-13dup)
n.458-11_458-8dup
c.278-11_278-8dup (n.278-11_278-8dup)
c.223-16_223-13dup (n.223-16_223-13dup)
 gnomAD v3 gnomAD v4
18g.62358236_62358240dupCA991036090TNFRSF11Ac.428-12_428-8dup (n.428-12_428-8dup)
n.334_338dup
c.428-54_428-50dup (n.428-54_428-50dup)
c.443-12_443-8dup (n.443-12_443-8dup)
c.325-17_325-13dup (n.325-17_325-13dup)
n.458-12_458-8dup
c.278-12_278-8dup (n.278-12_278-8dup)
c.223-17_223-13dup (n.223-17_223-13dup)
 dbSNP gnomAD v3 gnomAD v4
18g.62358235_62358240dupCA2642068175TNFRSF11Ac.428-13_428-8dup (n.428-13_428-8dup)
n.333_338dup
c.428-55_428-50dup (n.428-55_428-50dup)
c.443-13_443-8dup (n.443-13_443-8dup)
c.325-18_325-13dup (n.325-18_325-13dup)
n.458-13_458-8dup
c.278-13_278-8dup (n.278-13_278-8dup)
c.223-18_223-13dup (n.223-18_223-13dup)
 gnomAD v4
18g.62358234_62358240dupCA2642068173TNFRSF11Ac.428-14_428-8dup (n.428-14_428-8dup)
n.332_338dup
c.428-56_428-50dup (n.428-56_428-50dup)
c.443-14_443-8dup (n.443-14_443-8dup)
c.325-19_325-13dup (n.325-19_325-13dup)
n.458-14_458-8dup
c.278-14_278-8dup (n.278-14_278-8dup)
c.223-19_223-13dup (n.223-19_223-13dup)
 gnomAD v4
18g.62358233_62358240dupCA2642068174TNFRSF11Ac.428-15_428-8dup (n.428-15_428-8dup)
n.331_338dup
c.428-57_428-50dup (n.428-57_428-50dup)
c.443-15_443-8dup (n.443-15_443-8dup)
c.325-20_325-13dup (n.325-20_325-13dup)
n.458-15_458-8dup
c.278-15_278-8dup (n.278-15_278-8dup)
c.223-20_223-13dup (n.223-20_223-13dup)
 gnomAD v4
18g.62358231_62358240dupCA920001988TNFRSF11Ac.428-17_428-8dup (n.428-17_428-8dup)
n.329_338dup
c.428-59_428-50dup (n.428-59_428-50dup)
c.443-17_443-8dup (n.443-17_443-8dup)
c.325-22_325-13dup (n.325-22_325-13dup)
n.458-17_458-8dup
c.278-17_278-8dup (n.278-17_278-8dup)
c.223-22_223-13dup (n.223-22_223-13dup)
 dbSNP
18g.62358229_62358240dupCA991036092TNFRSF11Ac.428-19_428-8dup (n.428-19_428-8dup)
n.327_338dup
c.428-61_428-50dup (n.428-61_428-50dup)
c.443-19_443-8dup (n.443-19_443-8dup)
c.325-24_325-13dup (n.325-24_325-13dup)
n.458-19_458-8dup
c.278-19_278-8dup (n.278-19_278-8dup)
c.223-24_223-13dup (n.223-24_223-13dup)
 gnomAD v3 gnomAD v4
18g.62358240delCA8983753TNFRSF11Ac.428-8del (n.428-8del)
n.338del
c.428-50del (n.428-50del)
c.443-8del (n.443-8del)
c.325-13del (n.325-13del)
n.458-8del
c.278-8del (n.278-8del)
c.223-13del (n.223-13del)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
18g.62358239_62358240delCA8983752TNFRSF11Ac.428-9_428-8del (n.428-9_428-8del)
n.337_338del
c.428-51_428-50del (n.428-51_428-50del)
c.443-9_443-8del (n.443-9_443-8del)
c.325-14_325-13del (n.325-14_325-13del)
n.458-9_458-8del
c.278-9_278-8del (n.278-9_278-8del)
c.223-14_223-13del (n.223-14_223-13del)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
18g.62358238_62358240delCA8983751TNFRSF11Ac.428-10_428-8del (n.428-10_428-8del)
n.336_338del
c.428-52_428-50del (n.428-52_428-50del)
c.443-10_443-8del (n.443-10_443-8del)
c.325-15_325-13del (n.325-15_325-13del)
n.458-10_458-8del
c.278-10_278-8del (n.278-10_278-8del)
c.223-15_223-13del (n.223-15_223-13del)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
18g.62358237_62358240delCA2573029451TNFRSF11Ac.428-11_428-8del (n.428-11_428-8del)
n.335_338del
c.428-53_428-50del (n.428-53_428-50del)
c.443-11_443-8del (n.443-11_443-8del)
c.325-16_325-13del (n.325-16_325-13del)
n.458-11_458-8del
c.278-11_278-8del (n.278-11_278-8del)
c.223-16_223-13del (n.223-16_223-13del)
 gnomAD v4
18g.62358236_62358240delCA2642068171TNFRSF11Ac.428-12_428-8del (n.428-12_428-8del)
n.334_338del
c.428-54_428-50del (n.428-54_428-50del)
c.443-12_443-8del (n.443-12_443-8del)
c.325-17_325-13del (n.325-17_325-13del)
n.458-12_458-8del
c.278-12_278-8del (n.278-12_278-8del)
c.223-17_223-13del (n.223-17_223-13del)
 dbSNP gnomAD v4
18g.62358235_62358240delCA2642068172TNFRSF11Ac.428-13_428-8del (n.428-13_428-8del)
n.333_338del
c.428-55_428-50del (n.428-55_428-50del)
c.443-13_443-8del (n.443-13_443-8del)
c.325-18_325-13del (n.325-18_325-13del)
n.458-13_458-8del
c.278-13_278-8del (n.278-13_278-8del)
c.223-18_223-13del (n.223-18_223-13del)
 gnomAD v4
18g.62358231T>CCA2642068179TNFRSF11Ac.428-17T>C (n.428-17T>C)
n.329T>C
c.428-59T>C (n.428-59T>C)
c.443-17T>C (n.443-17T>C)
c.325-22T>C (n.325-22T>C)
n.458-17T>C
c.278-17T>C (n.278-17T>C)
c.223-22T>C (n.223-22T>C)
 gnomAD v4
18g.62358231T>GCA2576518620TNFRSF11Ac.428-17T>G (n.428-17T>G)
n.329T>G
c.428-59T>G (n.428-59T>G)
c.443-17T>G (n.443-17T>G)
c.325-22T>G (n.325-22T>G)
n.458-17T>G
c.278-17T>G (n.278-17T>G)
c.223-22T>G (n.223-22T>G)
18g.62358231T=CA2308284500TNFRSF11Ac.428-17T= (n.428-17T=)
n.329T=
c.428-59T= (n.428-59T=)
c.443-17T= (n.443-17T=)
c.325-22T= (n.325-22T=)
n.458-17T=
c.278-17T= (n.278-17T=)
c.223-22T= (n.223-22T=)
18g.62358231_62358232insGCA630114090TNFRSF11Ac.428-17_428-16insG (n.428-17_428-16insG)
n.329_330insG
c.428-59_428-58insG (n.428-59_428-58insG)
c.443-17_443-16insG (n.443-17_443-16insG)
c.325-22_325-21insG (n.325-22_325-21insG)
n.458-17_458-16insG
c.278-17_278-16insG (n.278-17_278-16insG)
c.223-22_223-21insG (n.223-22_223-21insG)
 dbSNP gnomAD v2 gnomAD v4
18g.62358232T>ACA2740091821TNFRSF11Ac.428-16T>A (n.428-16T>A)
n.330T>A
c.428-58T>A (n.428-58T>A)
c.443-16T>A (n.443-16T>A)
c.325-21T>A (n.325-21T>A)
n.458-16T>A
c.278-16T>A (n.278-16T>A)
c.223-21T>A (n.223-21T>A)
 ClinVar
18g.62358232T>CCA2642068180TNFRSF11Ac.428-16T>C (n.428-16T>C)
n.330T>C
c.428-58T>C (n.428-58T>C)
c.443-16T>C (n.443-16T>C)
c.325-21T>C (n.325-21T>C)
n.458-16T>C
c.278-16T>C (n.278-16T>C)
c.223-21T>C (n.223-21T>C)
 dbSNP gnomAD v4
18g.62358232_62358233insGCA2576518621TNFRSF11Ac.428-16_428-15insG (n.428-16_428-15insG)
n.330_331insG
c.428-58_428-57insG (n.428-58_428-57insG)
c.443-16_443-15insG (n.443-16_443-15insG)
c.325-21_325-20insG (n.325-21_325-20insG)
n.458-16_458-15insG
c.278-16_278-15insG (n.278-16_278-15insG)
c.223-21_223-20insG (n.223-21_223-20insG)
18g.62358233T>ACA2642068182TNFRSF11Ac.428-15T>A (n.428-15T>A)
n.331T>A
c.428-57T>A (n.428-57T>A)
c.443-15T>A (n.443-15T>A)
c.325-20T>A (n.325-20T>A)
n.458-15T>A
c.278-15T>A (n.278-15T>A)
c.223-20T>A (n.223-20T>A)
 gnomAD v4
18g.62358233T>CCA2576518622TNFRSF11Ac.428-15T>C (n.428-15T>C)
n.331T>C
c.428-57T>C (n.428-57T>C)
c.443-15T>C (n.443-15T>C)
c.325-20T>C (n.325-20T>C)
n.458-15T>C
c.278-15T>C (n.278-15T>C)
c.223-20T>C (n.223-20T>C)
 gnomAD v4
18g.62358233_62358234insCTCA2642068181TNFRSF11Ac.428-15_428-14insCT (n.428-15_428-14insCT)
n.331_332insCT
c.428-57_428-56insCT (n.428-57_428-56insCT)
c.443-15_443-14insCT (n.443-15_443-14insCT)
c.325-20_325-19insCT (n.325-20_325-19insCT)
n.458-15_458-14insCT
c.278-15_278-14insCT (n.278-15_278-14insCT)
c.223-20_223-19insCT (n.223-20_223-19insCT)
 gnomAD v4
18g.62358234T>ACA2642068183TNFRSF11Ac.428-14T>A (n.428-14T>A)
n.332T>A
c.428-56T>A (n.428-56T>A)
c.443-14T>A (n.443-14T>A)
c.325-19T>A (n.325-19T>A)
n.458-14T>A
c.278-14T>A (n.278-14T>A)
c.223-19T>A (n.223-19T>A)
 gnomAD v4
18g.62358234T>GCA301696738TNFRSF11Ac.428-14T>G (n.428-14T>G)
n.332T>G
c.428-56T>G (n.428-56T>G)
c.443-14T>G (n.443-14T>G)
c.325-19T>G (n.325-19T>G)
n.458-14T>G
c.278-14T>G (n.278-14T>G)
c.223-19T>G (n.223-19T>G)
 dbSNP gnomAD v3 gnomAD v4
18g.62358234T=CA2308284501TNFRSF11Ac.428-14T= (n.428-14T=)
n.332T=
c.428-56T= (n.428-56T=)
c.443-14T= (n.443-14T=)
c.325-19T= (n.325-19T=)
n.458-14T=
c.278-14T= (n.278-14T=)
c.223-19T= (n.223-19T=)
18g.62358235T>ACA2642068184TNFRSF11Ac.428-13T>A (n.428-13T>A)
n.333T>A
c.428-55T>A (n.428-55T>A)
c.443-13T>A (n.443-13T>A)
c.325-18T>A (n.325-18T>A)
n.458-13T>A
c.278-13T>A (n.278-13T>A)
c.223-18T>A (n.223-18T>A)
 gnomAD v4
18g.62358235T>CCA2642068185TNFRSF11Ac.428-13T>C (n.428-13T>C)
n.333T>C
c.428-55T>C (n.428-55T>C)
c.443-13T>C (n.443-13T>C)
c.325-18T>C (n.325-18T>C)
n.458-13T>C
c.278-13T>C (n.278-13T>C)
c.223-18T>C (n.223-18T>C)
 gnomAD v4
18g.62358236T>ACA2642068186TNFRSF11Ac.428-12T>A (n.428-12T>A)
n.334T>A
c.428-54T>A (n.428-54T>A)
c.443-12T>A (n.443-12T>A)
c.325-17T>A (n.325-17T>A)
n.458-12T>A
c.278-12T>A (n.278-12T>A)
c.223-17T>A (n.223-17T>A)
 gnomAD v4
18g.62358236T>CCA2642068187TNFRSF11Ac.428-12T>C (n.428-12T>C)
n.334T>C
c.428-54T>C (n.428-54T>C)
c.443-12T>C (n.443-12T>C)
c.325-17T>C (n.325-17T>C)
n.458-12T>C
c.278-12T>C (n.278-12T>C)
c.223-17T>C (n.223-17T>C)
 gnomAD v4
18g.62358237T>CCA2642068189TNFRSF11Ac.428-11T>C (n.428-11T>C)
n.335T>C
c.428-53T>C (n.428-53T>C)
c.443-11T>C (n.443-11T>C)
c.325-16T>C (n.325-16T>C)
n.458-11T>C
c.278-11T>C (n.278-11T>C)
c.223-16T>C (n.223-16T>C)
 ClinVar gnomAD v4
18g.62358240_62358241insTTTTTCTTTTCA2642068188TNFRSF11Ac.428-8_428-7insTTTTTCTTTT (n.428-8_428-7insTTTTTCTTTT)
n.338_339insTTTTTCTTTT
c.428-50_428-49insTTTTTCTTTT (n.428-50_428-49insTTTTTCTTTT)
c.443-8_443-7insTTTTTCTTTT (n.443-8_443-7insTTTTTCTTTT)
c.325-13_325-12insTTTTTCTTTT (n.325-13_325-12insTTTTTCTTTT)
n.458-8_458-7insTTTTTCTTTT
c.278-8_278-7insTTTTTCTTTT (n.278-8_278-7insTTTTTCTTTT)
c.223-13_223-12insTTTTTCTTTT (n.223-13_223-12insTTTTTCTTTT)
 gnomAD v4
18g.62358238T>CCA781258322TNFRSF11Ac.428-10T>C (n.428-10T>C)
n.336T>C
c.428-52T>C (n.428-52T>C)
c.443-10T>C (n.443-10T>C)
c.325-15T>C (n.325-15T>C)
n.458-10T>C
c.278-10T>C (n.278-10T>C)
c.223-15T>C (n.223-15T>C)
 dbSNP gnomAD v4
18g.62358238T=CA2308284502TNFRSF11Ac.428-10T= (n.428-10T=)
n.336T=
c.428-52T= (n.428-52T=)
c.443-10T= (n.443-10T=)
c.325-15T= (n.325-15T=)
n.458-10T=
c.278-10T= (n.278-10T=)
c.223-15T= (n.223-15T=)
18g.62358239_62358240insCTTCA2812750064TNFRSF11Ac.428-9_428-8insCTT (n.428-9_428-8insCTT)
n.337_338insCTT
c.428-51_428-50insCTT (n.428-51_428-50insCTT)
c.443-9_443-8insCTT (n.443-9_443-8insCTT)
c.325-14_325-13insCTT (n.325-14_325-13insCTT)
n.458-9_458-8insCTT
c.278-9_278-8insCTT (n.278-9_278-8insCTT)
c.223-14_223-13insCTT (n.223-14_223-13insCTT)
18g.62358239_62358242delCA2642068190TNFRSF11Ac.428-9_428-6del (n.428-9_428-6del)
n.337_340del
c.428-51_428-48del (n.428-51_428-48del)
c.443-9_443-6del (n.443-9_443-6del)
c.325-14_325-11del (n.325-14_325-11del)
n.458-9_458-6del
c.278-9_278-6del (n.278-9_278-6del)
c.223-14_223-11del (n.223-14_223-11del)
 gnomAD v4
18g.62358239T>CCA301696739TNFRSF11Ac.428-9T>C (n.428-9T>C)
n.337T>C
c.428-51T>C (n.428-51T>C)
c.443-9T>C (n.443-9T>C)
c.325-14T>C (n.325-14T>C)
n.458-9T>C
c.278-9T>C (n.278-9T>C)
c.223-14T>C (n.223-14T>C)
 ClinVar dbSNP gnomAD v3 gnomAD v4
18g.62358239T=CA2308284503TNFRSF11Ac.428-9T= (n.428-9T=)
n.337T=
c.428-51T= (n.428-51T=)
c.443-9T= (n.443-9T=)
c.325-14T= (n.325-14T=)
n.458-9T=
c.278-9T= (n.278-9T=)
c.223-14T= (n.223-14T=)
18g.62358239_62358241delinsTTCCA2308284504TNFRSF11Ac.428-9_428-7delinsTTC (n.428-9_428-7delinsTTC)
n.337_339delinsTTC
c.428-51_428-49delinsTTC (n.428-51_428-49delinsTTC)
c.443-9_443-7delinsTTC (n.443-9_443-7delinsTTC)
c.325-14_325-12delinsTTC (n.325-14_325-12delinsTTC)
n.458-9_458-7delinsTTC
c.278-9_278-7delinsTTC (n.278-9_278-7delinsTTC)
c.223-14_223-12delinsTTC (n.223-14_223-12delinsTTC)
18g.62358240_62358242delCA2642068191TNFRSF11Ac.428-8_428-6del (n.428-8_428-6del)
n.338_340del
c.428-50_428-48del (n.428-50_428-48del)
c.443-8_443-6del (n.443-8_443-6del)
c.325-13_325-11del (n.325-13_325-11del)
n.458-8_458-6del
c.278-8_278-6del (n.278-8_278-6del)
c.223-13_223-11del (n.223-13_223-11del)
 gnomAD v4
18g.62358239_62358240insCCA2576518623TNFRSF11Ac.428-9_428-8insC (n.428-9_428-8insC)
n.337_338insC
c.428-51_428-50insC (n.428-51_428-50insC)
c.443-9_443-8insC (n.443-9_443-8insC)
c.325-14_325-13insC (n.325-14_325-13insC)
n.458-9_458-8insC
c.278-9_278-8insC (n.278-9_278-8insC)
c.223-14_223-13insC (n.223-14_223-13insC)
 gnomAD v4
18g.62358240T>ACA2642068192TNFRSF11Ac.428-8T>A (n.428-8T>A)
n.338T>A
c.428-50T>A (n.428-50T>A)
c.443-8T>A (n.443-8T>A)
c.325-13T>A (n.325-13T>A)
n.458-8T>A
c.278-8T>A (n.278-8T>A)
c.223-13T>A (n.223-13T>A)
 gnomAD v4
18g.62358240T>CCA8983763TNFRSF11Ac.428-8T>C (n.428-8T>C)
n.338T>C
c.428-50T>C (n.428-50T>C)
c.443-8T>C (n.443-8T>C)
c.325-13T>C (n.325-13T>C)
n.458-8T>C
c.278-8T>C (n.278-8T>C)
c.223-13T>C (n.223-13T>C)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
18g.62358240T=CA2308284505TNFRSF11Ac.428-8T= (n.428-8T=)
n.338T=
c.428-50T= (n.428-50T=)
c.443-8T= (n.443-8T=)
c.325-13T= (n.325-13T=)
n.458-8T=
c.278-8T= (n.278-8T=)
c.223-13T= (n.223-13T=)
18g.62358240_62358241delinsTCCA2308284506TNFRSF11Ac.428-8_428-7delinsTC (n.428-8_428-7delinsTC)
n.338_339delinsTC
c.428-50_428-49delinsTC (n.428-50_428-49delinsTC)
c.443-8_443-7delinsTC (n.443-8_443-7delinsTC)
c.325-13_325-12delinsTC (n.325-13_325-12delinsTC)
n.458-8_458-7delinsTC
c.278-8_278-7delinsTC (n.278-8_278-7delinsTC)
c.223-13_223-12delinsTC (n.223-13_223-12delinsTC)
18g.62358242_62358243delCA2308284507TNFRSF11Ac.428-6_428-5del (n.428-6_428-5del)
n.340_341del
c.428-48_428-47del (n.428-48_428-47del)
c.443-6_443-5del (n.443-6_443-5del)
c.325-11_325-10del (n.325-11_325-10del)
n.458-6_458-5del
c.278-6_278-5del (n.278-6_278-5del)
c.223-11_223-10del (n.223-11_223-10del)
 dbSNP gnomAD v4
18g.62358240_62358241insTTTTCCA2642068193TNFRSF11Ac.428-8_428-7insTTTTC (n.428-8_428-7insTTTTC)
n.338_339insTTTTC
c.428-50_428-49insTTTTC (n.428-50_428-49insTTTTC)
c.443-8_443-7insTTTTC (n.443-8_443-7insTTTTC)
c.325-13_325-12insTTTTC (n.325-13_325-12insTTTTC)
n.458-8_458-7insTTTTC
c.278-8_278-7insTTTTC (n.278-8_278-7insTTTTC)
c.223-13_223-12insTTTTC (n.223-13_223-12insTTTTC)
 gnomAD v4
18g.62358240_62358241insTTTTTCCA2642068194TNFRSF11Ac.428-8_428-7insTTTTTC (n.428-8_428-7insTTTTTC)
n.338_339insTTTTTC
c.428-50_428-49insTTTTTC (n.428-50_428-49insTTTTTC)
c.443-8_443-7insTTTTTC (n.443-8_443-7insTTTTTC)
c.325-13_325-12insTTTTTC (n.325-13_325-12insTTTTTC)
n.458-8_458-7insTTTTTC
c.278-8_278-7insTTTTTC (n.278-8_278-7insTTTTTC)
c.223-13_223-12insTTTTTC (n.223-13_223-12insTTTTTC)
 gnomAD v4
18g.62358241delCA8983762TNFRSF11Ac.428-7del (n.428-7del)
n.339del
c.428-49del (n.428-49del)
c.443-7del (n.443-7del)
c.325-12del (n.325-12del)
n.458-7del
c.278-7del (n.278-7del)
c.223-12del (n.223-12del)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
18g.62358241C>ACA301696747TNFRSF11Ac.428-7C>A (n.428-7C>A)
n.339C>A
c.428-49C>A (n.428-49C>A)
c.443-7C>A (n.443-7C>A)
c.325-12C>A (n.325-12C>A)
n.458-7C>A
c.278-7C>A (n.278-7C>A)
c.223-12C>A (n.223-12C>A)
 dbSNP gnomAD v4
18g.62358241C=CA2308284508TNFRSF11Ac.428-7C= (n.428-7C=)
n.339C=
c.428-49C= (n.428-49C=)
c.443-7C= (n.443-7C=)
c.325-12C= (n.325-12C=)
n.458-7C=
c.278-7C= (n.278-7C=)
c.223-12C= (n.223-12C=)
18g.62358241C>GCA2642068195TNFRSF11Ac.428-7C>G (n.428-7C>G)
n.339C>G
c.428-49C>G (n.428-49C>G)
c.443-7C>G (n.443-7C>G)
c.325-12C>G (n.325-12C>G)
n.458-7C>G
c.278-7C>G (n.278-7C>G)
c.223-12C>G (n.223-12C>G)
 gnomAD v4
18g.62358241C>TCA8983764TNFRSF11Ac.428-7C>T (n.428-7C>T)
n.339C>T
c.428-49C>T (n.428-49C>T)
c.443-7C>T (n.443-7C>T)
c.325-12C>T (n.325-12C>T)
n.458-7C>T
c.278-7C>T (n.278-7C>T)
c.223-12C>T (n.223-12C>T)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
18g.62358241dupCA630114096TNFRSF11Ac.428-7dup (n.428-7dup)
n.339dup
c.428-49dup (n.428-49dup)
c.443-7dup (n.443-7dup)
c.325-12dup (n.325-12dup)
n.458-7dup
c.278-7dup (n.278-7dup)
c.223-12dup (n.223-12dup)
 dbSNP gnomAD v2
18g.62358242T>ACA2642068196TNFRSF11Ac.428-6T>A (n.428-6T>A)
n.340T>A
c.428-48T>A (n.428-48T>A)
c.443-6T>A (n.443-6T>A)
c.325-11T>A (n.325-11T>A)
n.458-6T>A
c.278-6T>A (n.278-6T>A)
c.223-11T>A (n.223-11T>A)
 gnomAD v4
18g.62358242T>CCA2642068197TNFRSF11Ac.428-6T>C (n.428-6T>C)
n.340T>C
c.428-48T>C (n.428-48T>C)
c.443-6T>C (n.443-6T>C)
c.325-11T>C (n.325-11T>C)
n.458-6T>C
c.278-6T>C (n.278-6T>C)
c.223-11T>C (n.223-11T>C)
 gnomAD v4
18g.62358242_62358244delinsTCACA2308284509TNFRSF11Ac.428-6_428-4delinsTCA (n.428-6_428-4delinsTCA)
n.340_342delinsTCA
c.428-48_428-46delinsTCA (n.428-48_428-46delinsTCA)
c.443-6_443-4delinsTCA (n.443-6_443-4delinsTCA)
c.325-11_325-9delinsTCA (n.325-11_325-9delinsTCA)
n.458-6_458-4delinsTCA
c.278-6_278-4delinsTCA (n.278-6_278-4delinsTCA)
c.223-11_223-9delinsTCA (n.223-11_223-9delinsTCA)
18g.62358242_62358243insAACA2576518624TNFRSF11Ac.428-6_428-5insAA (n.428-6_428-5insAA)
n.340_341insAA
c.428-48_428-47insAA (n.428-48_428-47insAA)
c.443-6_443-5insAA (n.443-6_443-5insAA)
c.325-11_325-10insAA (n.325-11_325-10insAA)
n.458-6_458-5insAA
c.278-6_278-5insAA (n.278-6_278-5insAA)
c.223-11_223-10insAA (n.223-11_223-10insAA)
 gnomAD v4
18g.62358243C>ACA2564664270TNFRSF11Ac.428-5C>A (n.428-5C>A)
n.341C>A
c.428-47C>A (n.428-47C>A)
c.443-5C>A (n.443-5C>A)
c.325-10C>A (n.325-10C>A)
n.458-5C>A
c.278-5C>A (n.278-5C>A)
c.223-10C>A (n.223-10C>A)
 dbSNP gnomAD v4
18g.62358243C=CA2308284510TNFRSF11Ac.428-5C= (n.428-5C=)
n.341C=
c.428-47C= (n.428-47C=)
c.443-5C= (n.443-5C=)
c.325-10C= (n.325-10C=)
n.458-5C=
c.278-5C= (n.278-5C=)
c.223-10C= (n.223-10C=)
18g.62358243C>GCA2642068198TNFRSF11Ac.428-5C>G (n.428-5C>G)
n.341C>G
c.428-47C>G (n.428-47C>G)
c.443-5C>G (n.443-5C>G)
c.325-10C>G (n.325-10C>G)
n.458-5C>G
c.278-5C>G (n.278-5C>G)
c.223-10C>G (n.223-10C>G)
 gnomAD v4
18g.62358243C>TCA630114100TNFRSF11Ac.428-5C>T (n.428-5C>T)
n.341C>T
c.428-47C>T (n.428-47C>T)
c.443-5C>T (n.443-5C>T)
c.325-10C>T (n.325-10C>T)
n.458-5C>T
c.278-5C>T (n.278-5C>T)
c.223-10C>T (n.223-10C>T)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
18g.62358243_62358245delCA991036107TNFRSF11Ac.428-5_428-3del (n.428-5_428-3del)
n.341_343del
c.428-47_428-45del (n.428-47_428-45del)
c.443-5_443-3del (n.443-5_443-3del)
c.325-10_325-8del (n.325-10_325-8del)
n.458-5_458-3del
c.278-5_278-3del (n.278-5_278-3del)
c.223-10_223-8del (n.223-10_223-8del)
 gnomAD v3 gnomAD v4
18g.62358243_62358246delCA991036110TNFRSF11Ac.428-5_428-2del (n.428-5_428-2del)
n.341_344del
c.428-47_428-44del (n.428-47_428-44del)
c.443-5_443-2del (n.443-5_443-2del)
c.325-10_325-7del (n.325-10_325-7del)
n.458-5_458-2del
c.278-5_278-2del (n.278-5_278-2del)
c.223-10_223-7del (n.223-10_223-7del)
 gnomAD v3 gnomAD v4
18g.62358245_62358246delCA630114099TNFRSF11Ac.428-3_428-2del (n.428-3_428-2del)
n.343_344del
c.428-45_428-44del (n.428-45_428-44del)
c.443-3_443-2del (n.443-3_443-2del)
c.325-8_325-7del (n.325-8_325-7del)
n.458-3_458-2del
c.278-3_278-2del (n.278-3_278-2del)
c.223-8_223-7del (n.223-8_223-7del)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
18g.62358243_62358247delCA991036113TNFRSF11Ac.428-5_428-1del (n.428-5_428-1del)
n.341_345del
c.428-47_428-43del (n.428-47_428-43del)
c.443-5_443-1del (n.443-5_443-1del)
c.325-10_325-6del (n.325-10_325-6del)
n.458-5_458-1del
c.278-5_278-1del (n.278-5_278-1del)
c.223-10_223-6del (n.223-10_223-6del)
 gnomAD v3 gnomAD v4
18g.62358243_62358253delCA2642068199TNFRSF11Ac.428-5_433del
n.341_351del
c.428-47_428-37del (n.428-47_428-37del)
c.443-5_448del
c.325-10_325del
n.458-5_463del
c.278-5_283del
c.223-10_223del
 gnomAD v4
18g.62358244_62358253delCA2812750065TNFRSF11Ac.428-4_433del
n.342_351del
c.428-46_428-37del (n.428-46_428-37del)
c.443-4_448del
c.325-9_325del
n.458-4_463del
c.278-4_283del
c.223-9_223del
18g.62358244delCA2576518625TNFRSF11Ac.428-4del (n.428-4del)
n.342del
c.428-46del (n.428-46del)
c.443-4del (n.443-4del)
c.325-9del (n.325-9del)
n.458-4del
c.278-4del (n.278-4del)
c.223-9del (n.223-9del)
18g.62358244A=CA2308284511TNFRSF11Ac.428-4A= (n.428-4A=)
n.342A=
c.428-46A= (n.428-46A=)
c.443-4A= (n.443-4A=)
c.325-9A= (n.325-9A=)
n.458-4A=
c.278-4A= (n.278-4A=)
c.223-9A= (n.223-9A=)
18g.62358244A>CCA991036119TNFRSF11Ac.428-4A>C (n.428-4A>C)
n.342A>C
c.428-46A>C (n.428-46A>C)
c.443-4A>C (n.443-4A>C)
c.325-9A>C (n.325-9A>C)
n.458-4A>C
c.278-4A>C (n.278-4A>C)
c.223-9A>C (n.223-9A>C)
 gnomAD v3 gnomAD v4
18g.62358244A>GCA2642068201TNFRSF11Ac.428-4A>G (n.428-4A>G)
n.342A>G
c.428-46A>G (n.428-46A>G)
c.443-4A>G (n.443-4A>G)
c.325-9A>G (n.325-9A>G)
n.458-4A>G
c.278-4A>G (n.278-4A>G)
c.223-9A>G (n.223-9A>G)
 gnomAD v4
18g.62358244A>TCA630114102TNFRSF11Ac.428-4A>T (n.428-4A>T)
n.342A>T
c.428-46A>T (n.428-46A>T)
c.443-4A>T (n.443-4A>T)
c.325-9A>T (n.325-9A>T)
n.458-4A>T
c.278-4A>T (n.278-4A>T)
c.223-9A>T (n.223-9A>T)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
18g.62358244_62358245insAACA2642068200TNFRSF11Ac.428-4_428-3insAA (n.428-4_428-3insAA)
n.342_343insAA
c.428-46_428-45insAA (n.428-46_428-45insAA)
c.443-4_443-3insAA (n.443-4_443-3insAA)
c.325-9_325-8insAA (n.325-9_325-8insAA)
n.458-4_458-3insAA
c.278-4_278-3insAA (n.278-4_278-3insAA)
c.223-9_223-8insAA (n.223-9_223-8insAA)
 gnomAD v4
18g.62358244_62358245insTTTCA630114103TNFRSF11Ac.428-4_428-3insTTT (n.428-4_428-3insTTT)
n.342_343insTTT
c.428-46_428-45insTTT (n.428-46_428-45insTTT)
c.443-4_443-3insTTT (n.443-4_443-3insTTT)
c.325-9_325-8insTTT (n.325-9_325-8insTTT)
n.458-4_458-3insTTT
c.278-4_278-3insTTT (n.278-4_278-3insTTT)
c.223-9_223-8insTTT (n.223-9_223-8insTTT)
 dbSNP gnomAD v2
18g.62358245C>ACA991036129TNFRSF11Ac.428-3C>A (n.428-3C>A)
n.343C>A
c.428-45C>A (n.428-45C>A)
c.443-3C>A (n.443-3C>A)
c.325-8C>A (n.325-8C>A)
n.458-3C>A
c.278-3C>A (n.278-3C>A)
c.223-8C>A (n.223-8C>A)
 gnomAD v3 gnomAD v4
18g.62358245C>TCA991036131TNFRSF11Ac.428-3C>T (n.428-3C>T)
n.343C>T
c.428-45C>T (n.428-45C>T)
c.443-3C>T (n.443-3C>T)
c.325-8C>T (n.325-8C>T)
n.458-3C>T
c.278-3C>T (n.278-3C>T)
c.223-8C>T (n.223-8C>T)
 gnomAD v3 gnomAD v4
18g.62358246A>CCA402612842TNFRSF11Ac.428-2A>C (n.428-2A>C)
n.344A>C
c.428-44A>C (n.428-44A>C)
c.443-2A>C (n.443-2A>C)
c.325-7A>C (n.325-7A>C)
n.458-2A>C
c.278-2A>C (n.278-2A>C)
c.223-7A>C (n.223-7A>C)
 gnomAD v4
18g.62358246A>GCA402612844TNFRSF11Ac.428-2A>G (n.428-2A>G)
n.344A>G
c.428-44A>G (n.428-44A>G)
c.443-2A>G (n.443-2A>G)
c.325-7A>G (n.325-7A>G)
n.458-2A>G
c.278-2A>G (n.278-2A>G)
c.223-7A>G (n.223-7A>G)
 gnomAD v3 gnomAD v4
18g.62358246A>TCA402612848TNFRSF11Ac.428-2A>T (n.428-2A>T)
n.344A>T
c.428-44A>T (n.428-44A>T)
c.443-2A>T (n.443-2A>T)
c.325-7A>T (n.325-7A>T)
n.458-2A>T
c.278-2A>T (n.278-2A>T)
c.223-7A>T (n.223-7A>T)
 gnomAD v3 gnomAD v4
18g.62358247G>ACA402612852TNFRSF11Ac.428-1G>A (n.428-1G>A)
n.345G>A
c.428-43G>A (n.428-43G>A)
c.443-1G>A (n.443-1G>A)
c.325-6G>A (n.325-6G>A)
n.458-1G>A
c.278-1G>A (n.278-1G>A)
c.223-6G>A (n.223-6G>A)
 gnomAD v4
18g.62358247G>CCA402612855TNFRSF11Ac.428-1G>C (n.428-1G>C)
n.345G>C
c.428-43G>C (n.428-43G>C)
c.443-1G>C (n.443-1G>C)
c.325-6G>C (n.325-6G>C)
n.458-1G>C
c.278-1G>C (n.278-1G>C)
c.223-6G>C (n.223-6G>C)
 gnomAD v4
18g.62358247G>TCA402612856TNFRSF11Ac.428-1G>T (n.428-1G>T)
n.345G>T
c.428-43G>T (n.428-43G>T)
c.443-1G>T (n.443-1G>T)
c.325-6G>T (n.325-6G>T)
n.458-1G>T
c.278-1G>T (n.278-1G>T)
c.223-6G>T (n.223-6G>T)
 gnomAD v3 gnomAD v4
18g.62358248T>ACA402612859TNFRSF11Ac.428T>A (p.Leu143Ter)
n.346T>A
c.428-42T>A (n.428-42T>A)
c.443T>A (p.Leu148Ter)
c.325-5T>A (n.325-5T>A)
n.458T>A
c.278T>A (p.Leu93Ter)
c.223-5T>A (n.223-5T>A)
18g.62358248T>CCA8983765TNFRSF11Ac.428T>C (p.Leu143Ser)
n.346T>C
c.428-42T>C (n.428-42T>C)
c.443T>C (p.Leu148Ser)
c.325-5T>C (n.325-5T>C)
n.458T>C
c.278T>C (p.Leu93Ser)
c.223-5T>C (n.223-5T>C)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
18g.62358248T>GCA402612869TNFRSF11Ac.428T>G (p.Leu143Trp)
n.346T>G
c.428-42T>G (n.428-42T>G)
c.443T>G (p.Leu148Trp)
c.325-5T>G (n.325-5T>G)
n.458T>G
c.278T>G (p.Leu93Trp)
c.223-5T>G (n.223-5T>G)
 gnomAD v4
18g.62358248T=CA2308284512TNFRSF11Ac.428T= (p.Leu143=)
n.346T=
c.428-42T= (n.428-42T=)
c.443T= (p.Leu148=)
c.325-5T= (n.325-5T=)
n.458T=
c.278T= (p.Leu93=)
c.223-5T= (n.223-5T=)
18g.62358249G>ACA504077836TNFRSF11Ac.429G>A (p.Leu143=)
n.347G>A
c.428-41G>A (n.428-41G>A)
c.444G>A (p.Leu148=)
c.325-4G>A (n.325-4G>A)
n.459G>A
c.279G>A (p.Leu93=)
c.223-4G>A (n.223-4G>A)
 gnomAD v4
18g.62358249G>CCA402612872TNFRSF11Ac.429G>C (p.Leu143Phe)
n.347G>C
c.428-41G>C (n.428-41G>C)
c.444G>C (p.Leu148Phe)
c.325-4G>C (n.325-4G>C)
n.459G>C
c.279G>C (p.Leu93Phe)
c.223-4G>C (n.223-4G>C)
18g.62358249G>TCA402612874TNFRSF11Ac.429G>T (p.Leu143Phe)
n.347G>T
c.428-41G>T (n.428-41G>T)
c.444G>T (p.Leu148Phe)
c.325-4G>T (n.325-4G>T)
n.459G>T
c.279G>T (p.Leu93Phe)
c.223-4G>T (n.223-4G>T)
 gnomAD v3 gnomAD v4 COSMIC
18g.62358249_62358253delCA991036139TNFRSF11Ac.429_433del (p.Leu143PhefsTer17)
n.347_351del
c.428-41_428-37del (n.428-41_428-37del)
c.444_448del (p.Leu148PhefsTer17)
c.325-4_325del
n.459_463del
c.279_283del (p.Leu93PhefsTer17)
c.223-4_223del
 gnomAD v3 gnomAD v4
18g.62358250C>ACA402612876TNFRSF11Ac.430C>A (p.Gln144Lys)
n.348C>A
c.428-40C>A (n.428-40C>A)
c.445C>A (p.Gln149Lys)
c.325-3C>A (n.325-3C>A)
n.460C>A
c.280C>A (p.Gln94Lys)
c.223-3C>A (n.223-3C>A)
 dbSNP gnomAD v4
18g.62358250C=CA2308284513TNFRSF11Ac.430C= (p.Gln144=)
n.348C=
c.428-40C= (n.428-40C=)
c.445C= (p.Gln149=)
c.325-3C= (n.325-3C=)
n.460C=
c.280C= (p.Gln94=)
c.223-3C= (n.223-3C=)
18g.62358250C>GCA402612878TNFRSF11Ac.430C>G (p.Gln144Glu)
n.348C>G
c.428-40C>G (n.428-40C>G)
c.445C>G (p.Gln149Glu)
c.325-3C>G (n.325-3C>G)
n.460C>G
c.280C>G (p.Gln94Glu)
c.223-3C>G (n.223-3C>G)
18g.62358250C>TCA402612881TNFRSF11Ac.430C>T (p.Gln144Ter)
n.348C>T
c.428-40C>T (n.428-40C>T)
c.445C>T (p.Gln149Ter)
c.325-3C>T (n.325-3C>T)
n.460C>T
c.280C>T (p.Gln94Ter)
c.223-3C>T (n.223-3C>T)
 gnomAD v3 gnomAD v4
18g.62358250_62358251insTTTTTCA991036146TNFRSF11Ac.430_431insTTTTT (p.Gln144LeufsTer?)
n.348_349insTTTTT
c.428-40_428-39insTTTTT (n.428-40_428-39insTTTTT)
c.445_446insTTTTT (p.Gln149LeufsTer?)
c.325-3_325-2insTTTTT (n.325-3_325-2insTTTTT)
n.460_461insTTTTT
c.280_281insTTTTT (p.Gln94LeufsTer?)
c.223-3_223-2insTTTTT (n.223-3_223-2insTTTTT)
18g.62358251A>CCA402612883TNFRSF11Ac.431A>C (p.Gln144Pro)
n.349A>C
c.428-39A>C (n.428-39A>C)
c.446A>C (p.Gln149Pro)
c.325-2A>C (n.325-2A>C)
n.461A>C
c.281A>C (p.Gln94Pro)
c.223-2A>C (n.223-2A>C)
 gnomAD v3 gnomAD v4
18g.62358251A>GCA402612886TNFRSF11Ac.431A>G (p.Gln144Arg)
n.349A>G
c.428-39A>G (n.428-39A>G)
c.446A>G (p.Gln149Arg)
c.325-2A>G (n.325-2A>G)
n.461A>G
c.281A>G (p.Gln94Arg)
c.223-2A>G (n.223-2A>G)
 gnomAD v4
18g.62358251A>TCA402612892TNFRSF11Ac.431A>T (p.Gln144Leu)
n.349A>T
c.428-39A>T (n.428-39A>T)
c.446A>T (p.Gln149Leu)
c.325-2A>T (n.325-2A>T)
n.461A>T
c.281A>T (p.Gln94Leu)
c.223-2A>T (n.223-2A>T)
 gnomAD v3 gnomAD v4
18g.62358252G>ACA504077847TNFRSF11Ac.432G>A (p.Gln144=)
n.350G>A
c.428-38G>A (n.428-38G>A)
c.447G>A (p.Gln149=)
c.325-1G>A (n.325-1G>A)
n.462G>A
c.282G>A (p.Gln94=)
c.223-1G>A (n.223-1G>A)
 gnomAD v4
18g.62358252G>CCA402612898TNFRSF11Ac.432G>C (p.Gln144His)
n.350G>C
c.428-38G>C (n.428-38G>C)
c.447G>C (p.Gln149His)
c.325-1G>C (n.325-1G>C)
n.462G>C
c.282G>C (p.Gln94His)
c.223-1G>C (n.223-1G>C)
18g.62358252G>TCA402612899TNFRSF11Ac.432G>T (p.Gln144His)
n.350G>T
c.428-38G>T (n.428-38G>T)
c.447G>T (p.Gln149His)
c.325-1G>T (n.325-1G>T)
n.462G>T
c.282G>T (p.Gln94His)
c.223-1G>T (n.223-1G>T)
 gnomAD v3 gnomAD v4
18g.62358252_62358253insTTTTTTCA2812750066TNFRSF11Ac.432_433insTTTTTT (p.Gln144_Leu145insPhePhe)
n.350_351insTTTTTT
c.428-38_428-37insTTTTTT (n.428-38_428-37insTTTTTT)
c.447_448insTTTTTT (p.Gln149_Leu150insPhePhe)
c.325-1_325insTTTTTT (n.325-1_325insTTTTTT)
n.462_463insTTTTTT
c.282_283insTTTTTT (p.Gln94_Leu95insPhePhe)
c.223-1_223insTTTTTT (n.223-1_223insTTTTTT)
18g.62358253C>ACA402612900TNFRSF11Ac.433C>A (p.Leu145Ile)
n.351C>A
c.428-37C>A (n.428-37C>A)
c.448C>A (p.Leu150Ile)
c.325C>A (p.Leu109Ile)
n.463C>A
c.283C>A (p.Leu95Ile)
c.223C>A (p.Leu75Ile)
18g.62358253C>GCA402612901TNFRSF11Ac.433C>G (p.Leu145Val)
n.351C>G
c.428-37C>G (n.428-37C>G)
c.448C>G (p.Leu150Val)
c.325C>G (p.Leu109Val)
n.463C>G
c.283C>G (p.Leu95Val)
c.223C>G (p.Leu75Val)
 gnomAD v4
18g.62358253C>TCA402612902TNFRSF11Ac.433C>T (p.Leu145Phe)
n.351C>T
c.428-37C>T (n.428-37C>T)
c.448C>T (p.Leu150Phe)
c.325C>T (p.Leu109Phe)
n.463C>T
c.283C>T (p.Leu95Phe)
c.223C>T (p.Leu75Phe)
 gnomAD v3 gnomAD v4
18g.62358254T>ACA402612915TNFRSF11Ac.434T>A (p.Leu145His)
n.352T>A
c.428-36T>A (n.428-36T>A)
c.449T>A (p.Leu150His)
c.326T>A (p.Leu109His)
n.464T>A
c.284T>A (p.Leu95His)
c.224T>A (p.Leu75His)
 gnomAD v4
18g.62358254T>CCA402612912TNFRSF11Ac.434T>C (p.Leu145Pro)
n.352T>C
c.428-36T>C (n.428-36T>C)
c.449T>C (p.Leu150Pro)
c.326T>C (p.Leu109Pro)
n.464T>C
c.284T>C (p.Leu95Pro)
c.224T>C (p.Leu75Pro)
 gnomAD v4
18g.62358254T>GCA402612906TNFRSF11Ac.434T>G (p.Leu145Arg)
n.352T>G
c.428-36T>G (n.428-36T>G)
c.449T>G (p.Leu150Arg)
c.326T>G (p.Leu109Arg)
n.464T>G
c.284T>G (p.Leu95Arg)
c.224T>G (p.Leu75Arg)
18g.62358254_62358255insTTTTTTTTCA2812750067TNFRSF11Ac.434_435insTTTTTTTT (p.Asn146PhefsTer?)
n.352_353insTTTTTTTT
c.428-36_428-35insTTTTTTTT (n.428-36_428-35insTTTTTTTT)
c.449_450insTTTTTTTT (p.Asn151PhefsTer?)
c.326_327insTTTTTTTT (p.Asn110PhefsTer?)
n.464_465insTTTTTTTT
c.284_285insTTTTTTTT (p.Asn96PhefsTer?)
c.224_225insTTTTTTTT (p.Asn76PhefsTer?)
18g.62358255C>ACA504077860TNFRSF11Ac.435C>A (p.Leu145=)
n.353C>A
c.428-35C>A (n.428-35C>A)
c.450C>A (p.Leu150=)
c.327C>A (p.Leu109=)
n.465C>A
c.285C>A (p.Leu95=)
c.225C>A (p.Leu75=)
 dbSNP gnomAD v4
18g.62358255C>GCA504077862TNFRSF11Ac.435C>G (p.Leu145=)
n.353C>G
c.428-35C>G (n.428-35C>G)
c.450C>G (p.Leu150=)
c.327C>G (p.Leu109=)
n.465C>G
c.285C>G (p.Leu95=)
c.225C>G (p.Leu75=)
18g.62358255C>TCA504077864TNFRSF11Ac.435C>T (p.Leu145=)
n.353C>T
c.428-35C>T (n.428-35C>T)
c.450C>T (p.Leu150=)
c.327C>T (p.Leu109=)
n.465C>T
c.285C>T (p.Leu95=)
c.225C>T (p.Leu75=)
 gnomAD v3 gnomAD v4
18g.62358256A>CCA402612919TNFRSF11Ac.436A>C (p.Asn146His)
n.354A>C
c.428-34A>C (n.428-34A>C)
c.451A>C (p.Asn151His)
c.328A>C (p.Asn110His)
n.466A>C
c.286A>C (p.Asn96His)
c.226A>C (p.Asn76His)
18g.62358256A>GCA402612924TNFRSF11Ac.436A>G (p.Asn146Asp)
n.354A>G
c.428-34A>G (n.428-34A>G)
c.451A>G (p.Asn151Asp)
c.328A>G (p.Asn110Asp)
n.466A>G
c.286A>G (p.Asn96Asp)
c.226A>G (p.Asn76Asp)
18g.62358256A>TCA402612920TNFRSF11Ac.436A>T (p.Asn146Tyr)
n.354A>T
c.428-34A>T (n.428-34A>T)
c.451A>T (p.Asn151Tyr)
c.328A>T (p.Asn110Tyr)
n.466A>T
c.286A>T (p.Asn96Tyr)
c.226A>T (p.Asn76Tyr)
 gnomAD v3 gnomAD v4
18g.62358257A>CCA402612931TNFRSF11Ac.437A>C (p.Asn146Thr)
n.355A>C
c.428-33A>C (n.428-33A>C)
c.452A>C (p.Asn151Thr)
c.329A>C (p.Asn110Thr)
n.467A>C
c.287A>C (p.Asn96Thr)
c.227A>C (p.Asn76Thr)
18g.62358257A>GCA402612934TNFRSF11Ac.437A>G (p.Asn146Ser)
n.355A>G
c.428-33A>G (n.428-33A>G)
c.452A>G (p.Asn151Ser)
c.329A>G (p.Asn110Ser)
n.467A>G
c.287A>G (p.Asn96Ser)
c.227A>G (p.Asn76Ser)
 gnomAD v4
18g.62358257A>TCA402612936TNFRSF11Ac.437A>T (p.Asn146Ile)
n.355A>T
c.428-33A>T (n.428-33A>T)
c.452A>T (p.Asn151Ile)
c.329A>T (p.Asn110Ile)
n.467A>T
c.287A>T (p.Asn96Ile)
c.227A>T (p.Asn76Ile)
18g.62358258C>ACA402612939TNFRSF11Ac.438C>A (p.Asn146Lys)
n.356C>A
c.428-32C>A (n.428-32C>A)
c.453C>A (p.Asn151Lys)
c.330C>A (p.Asn110Lys)
n.468C>A
c.288C>A (p.Asn96Lys)
c.228C>A (p.Asn76Lys)
 dbSNP gnomAD v4
18g.62358258C>GCA402612942TNFRSF11Ac.438C>G (p.Asn146Lys)
n.356C>G
c.428-32C>G (n.428-32C>G)
c.453C>G (p.Asn151Lys)
c.330C>G (p.Asn110Lys)
n.468C>G
c.288C>G (p.Asn96Lys)
c.228C>G (p.Asn76Lys)
18g.62358258C>TCA504077878TNFRSF11Ac.438C>T (p.Asn146=)
n.356C>T
c.428-32C>T (n.428-32C>T)
c.453C>T (p.Asn151=)
c.330C>T (p.Asn110=)
n.468C>T
c.288C>T (p.Asn96=)
c.228C>T (p.Asn76=)
 gnomAD v3 gnomAD v4
18g.62358259A>CCA402612945TNFRSF11Ac.439A>C (p.Lys147Gln)
n.357A>C
c.428-31A>C (n.428-31A>C)
c.454A>C (p.Lys152Gln)
c.331A>C (p.Lys111Gln)
n.469A>C
c.289A>C (p.Lys97Gln)
c.229A>C (p.Lys77Gln)
18g.62358259A>GCA402612947TNFRSF11Ac.439A>G (p.Lys147Glu)
n.357A>G
c.428-31A>G (n.428-31A>G)
c.454A>G (p.Lys152Glu)
c.331A>G (p.Lys111Glu)
n.469A>G
c.289A>G (p.Lys97Glu)
c.229A>G (p.Lys77Glu)
 COSMIC
18g.62358259A>TCA402612950TNFRSF11Ac.439A>T (p.Lys147Ter)
n.357A>T
c.428-31A>T (n.428-31A>T)
c.454A>T (p.Lys152Ter)
c.331A>T (p.Lys111Ter)
n.469A>T
c.289A>T (p.Lys97Ter)
c.229A>T (p.Lys77Ter)
 gnomAD v3 gnomAD v4
18g.62358260A>CCA402612954TNFRSF11Ac.440A>C (p.Lys147Thr)
n.358A>C
c.428-30A>C (n.428-30A>C)
c.455A>C (p.Lys152Thr)
c.332A>C (p.Lys111Thr)
n.470A>C
c.290A>C (p.Lys97Thr)
c.230A>C (p.Lys77Thr)
18g.62358260A>GCA402612957TNFRSF11Ac.440A>G (p.Lys147Arg)
n.358A>G
c.428-30A>G (n.428-30A>G)
c.455A>G (p.Lys152Arg)
c.332A>G (p.Lys111Arg)
n.470A>G
c.290A>G (p.Lys97Arg)
c.230A>G (p.Lys77Arg)
18g.62358260A>TCA402612961TNFRSF11Ac.440A>T (p.Lys147Met)
n.358A>T
c.428-30A>T (n.428-30A>T)
c.455A>T (p.Lys152Met)
c.332A>T (p.Lys111Met)
n.470A>T
c.290A>T (p.Lys97Met)
c.230A>T (p.Lys77Met)
 gnomAD v3 gnomAD v4
18g.62358261G>ACA504077891TNFRSF11Ac.441G>A (p.Lys147=)
n.359G>A
c.428-29G>A (n.428-29G>A)
c.456G>A (p.Lys152=)
c.333G>A (p.Lys111=)
n.471G>A
c.291G>A (p.Lys97=)
c.231G>A (p.Lys77=)
18g.62358261G>CCA402612969TNFRSF11Ac.441G>C (p.Lys147Asn)
n.359G>C
c.428-29G>C (n.428-29G>C)
c.456G>C (p.Lys152Asn)
c.333G>C (p.Lys111Asn)
n.471G>C
c.291G>C (p.Lys97Asn)
c.231G>C (p.Lys77Asn)
18g.62358261G>TCA402612967TNFRSF11Ac.441G>T (p.Lys147Asn)
n.359G>T
c.428-29G>T (n.428-29G>T)
c.456G>T (p.Lys152Asn)
c.333G>T (p.Lys111Asn)
n.471G>T
c.291G>T (p.Lys97Asn)
c.231G>T (p.Lys77Asn)
 gnomAD v3 gnomAD v4
18g.62358262G>ACA402612972TNFRSF11Ac.442G>A (p.Asp148Asn)
n.360G>A
c.428-28G>A (n.428-28G>A)
c.457G>A (p.Asp153Asn)
c.334G>A (p.Asp112Asn)
n.472G>A
c.292G>A (p.Asp98Asn)
c.232G>A (p.Asp78Asn)
18g.62358262G>CCA402612973TNFRSF11Ac.442G>C (p.Asp148His)
n.360G>C
c.428-28G>C (n.428-28G>C)
c.457G>C (p.Asp153His)
c.334G>C (p.Asp112His)
n.472G>C
c.292G>C (p.Asp98His)
c.232G>C (p.Asp78His)
18g.62358262G>TCA402612974TNFRSF11Ac.442G>T (p.Asp148Tyr)
n.360G>T
c.428-28G>T (n.428-28G>T)
c.457G>T (p.Asp153Tyr)
c.334G>T (p.Asp112Tyr)
n.472G>T
c.292G>T (p.Asp98Tyr)
c.232G>T (p.Asp78Tyr)
 gnomAD v3 gnomAD v4
18g.62358263A>CCA402612978TNFRSF11Ac.443A>C (p.Asp148Ala)
n.361A>C
c.428-27A>C (n.428-27A>C)
c.458A>C (p.Asp153Ala)
c.335A>C (p.Asp112Ala)
n.473A>C
c.293A>C (p.Asp98Ala)
c.233A>C (p.Asp78Ala)
18g.62358263A>GCA402612981TNFRSF11Ac.443A>G (p.Asp148Gly)
n.361A>G
c.428-27A>G (n.428-27A>G)
c.458A>G (p.Asp153Gly)
c.335A>G (p.Asp112Gly)
n.473A>G
c.293A>G (p.Asp98Gly)
c.233A>G (p.Asp78Gly)
18g.62358263A>TCA402612986TNFRSF11Ac.443A>T (p.Asp148Val)
n.361A>T
c.428-27A>T (n.428-27A>T)
c.458A>T (p.Asp153Val)
c.335A>T (p.Asp112Val)
n.473A>T
c.293A>T (p.Asp98Val)
c.233A>T (p.Asp78Val)
 ClinVar gnomAD v3 gnomAD v4
18g.62358264C>ACA402612991TNFRSF11Ac.444C>A (p.Asp148Glu)
n.362C>A
c.428-26C>A (n.428-26C>A)
c.459C>A (p.Asp153Glu)
c.336C>A (p.Asp112Glu)
n.474C>A
c.294C>A (p.Asp98Glu)
c.234C>A (p.Asp78Glu)
 gnomAD v4
18g.62358264C>GCA402612994TNFRSF11Ac.444C>G (p.Asp148Glu)
n.362C>G
c.428-26C>G (n.428-26C>G)
c.459C>G (p.Asp153Glu)
c.336C>G (p.Asp112Glu)
n.474C>G
c.294C>G (p.Asp98Glu)
c.234C>G (p.Asp78Glu)
18g.62358264C>TCA504077904TNFRSF11Ac.444C>T (p.Asp148=)
n.362C>T
c.428-26C>T (n.428-26C>T)
c.459C>T (p.Asp153=)
c.336C>T (p.Asp112=)
n.474C>T
c.294C>T (p.Asp98=)
c.234C>T (p.Asp78=)
 gnomAD v3 gnomAD v4
18g.62358265A=CA2308284514TNFRSF11Ac.445A= (p.Thr149=)
n.363A=
c.428-25A= (n.428-25A=)
c.460A= (p.Thr154=)
c.337A= (p.Thr113=)
n.475A=
c.295A= (p.Thr99=)
c.235A= (p.Thr79=)
18g.62358265A>CCA402612996TNFRSF11Ac.445A>C (p.Thr149Pro)
n.363A>C
c.428-25A>C (n.428-25A>C)
c.460A>C (p.Thr154Pro)
c.337A>C (p.Thr113Pro)
n.475A>C
c.295A>C (p.Thr99Pro)
c.235A>C (p.Thr79Pro)
 gnomAD v3 gnomAD v4
18g.62358265A>GCA402612997TNFRSF11Ac.445A>G (p.Thr149Ala)
n.363A>G
c.428-25A>G (n.428-25A>G)
c.460A>G (p.Thr154Ala)
c.337A>G (p.Thr113Ala)
n.475A>G
c.295A>G (p.Thr99Ala)
c.235A>G (p.Thr79Ala)
 ClinVar dbSNP gnomAD v2 gnomAD v4
18g.62358265A>TCA402612998TNFRSF11Ac.445A>T (p.Thr149Ser)
n.363A>T
c.428-25A>T (n.428-25A>T)
c.460A>T (p.Thr154Ser)
c.337A>T (p.Thr113Ser)
n.475A>T
c.295A>T (p.Thr99Ser)
c.235A>T (p.Thr79Ser)
 gnomAD v4
18g.62358266C>ACA402613010TNFRSF11Ac.446C>A (p.Thr149Lys)
n.364C>A
c.428-24C>A (n.428-24C>A)
c.461C>A (p.Thr154Lys)
c.338C>A (p.Thr113Lys)
n.476C>A
c.296C>A (p.Thr99Lys)
c.236C>A (p.Thr79Lys)
18g.62358266C>GCA402613013TNFRSF11Ac.446C>G (p.Thr149Arg)
n.364C>G
c.428-24C>G (n.428-24C>G)
c.461C>G (p.Thr154Arg)
c.338C>G (p.Thr113Arg)
n.476C>G
c.296C>G (p.Thr99Arg)
c.236C>G (p.Thr79Arg)
18g.62358266C>TCA402613001TNFRSF11Ac.446C>T (p.Thr149Ile)
n.364C>T
c.428-24C>T (n.428-24C>T)
c.461C>T (p.Thr154Ile)
c.338C>T (p.Thr113Ile)
n.476C>T
c.296C>T (p.Thr99Ile)
c.236C>T (p.Thr79Ile)
 gnomAD v4
18g.62358266_62358268delinsCAGCA2308284515TNFRSF11Ac.446_448delinsCAG (p.Thr149=)
n.364_366delinsCAG
c.428-24_428-22delinsCAG (n.428-24_428-22delinsCAG)
c.461_463delinsCAG (p.Thr154=)
c.338_340delinsCAG (p.Thr113=)
n.476_478delinsCAG
c.296_298delinsCAG (p.Thr99=)
c.236_238delinsCAG (p.Thr79=)
18g.62358267A=CA2308284516TNFRSF11Ac.447A= (p.Thr149=)
n.365A=
c.428-23A= (n.428-23A=)
c.462A= (p.Thr154=)
c.339A= (p.Thr113=)
n.477A=
c.297A= (p.Thr99=)
c.237A= (p.Thr79=)
18g.62358267A>CCA504077911TNFRSF11Ac.447A>C (p.Thr149=)
n.365A>C
c.428-23A>C (n.428-23A>C)
c.462A>C (p.Thr154=)
c.339A>C (p.Thr113=)
n.477A>C
c.297A>C (p.Thr99=)
c.237A>C (p.Thr79=)
18g.62358267A>GCA8983766TNFRSF11Ac.447A>G (p.Thr149=)
n.365A>G
c.428-23A>G (n.428-23A>G)
c.462A>G (p.Thr154=)
c.339A>G (p.Thr113=)
n.477A>G
c.297A>G (p.Thr99=)
c.237A>G (p.Thr79=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
18g.62358267A>TCA8983767TNFRSF11Ac.447A>T (p.Thr149=)
n.365A>T
c.428-23A>T (n.428-23A>T)
c.462A>T (p.Thr154=)
c.339A>T (p.Thr113=)
n.477A>T
c.297A>T (p.Thr99=)
c.237A>T (p.Thr79=)
 dbSNP ExAC
18g.62358267_62358268delCA301696763TNFRSF11Ac.447_448del (p.Cys151GlnfsTer10)
n.365_366del
c.428-23_428-22del (n.428-23_428-22del)
c.462_463del (p.Cys156GlnfsTer10)
c.339_340del (p.Cys115GlnfsTer10)
n.477_478del
c.297_298del (p.Cys101GlnfsTer10)
c.237_238del (p.Cys81GlnfsTer10)
 ClinVar dbSNP gnomAD v3 gnomAD v4
18g.62358268G>ACA402613019TNFRSF11Ac.448G>A (p.Val150Met)
n.366G>A
c.428-22G>A (n.428-22G>A)
c.463G>A (p.Val155Met)
c.340G>A (p.Val114Met)
n.478G>A
c.298G>A (p.Val100Met)
c.238G>A (p.Val80Met)
18g.62358268G>CCA402613022TNFRSF11Ac.448G>C (p.Val150Leu)
n.366G>C
c.428-22G>C (n.428-22G>C)
c.463G>C (p.Val155Leu)
c.340G>C (p.Val114Leu)
n.478G>C
c.298G>C (p.Val100Leu)
c.238G>C (p.Val80Leu)
18g.62358268G>TCA402613028TNFRSF11Ac.448G>T (p.Val150Leu)
n.366G>T
c.428-22G>T (n.428-22G>T)
c.463G>T (p.Val155Leu)
c.340G>T (p.Val114Leu)
n.478G>T
c.298G>T (p.Val100Leu)
c.238G>T (p.Val80Leu)
 gnomAD v3 gnomAD v4
18g.62358269T>ACA402613031TNFRSF11Ac.449T>A (p.Val150Glu)
n.367T>A
c.428-21T>A (n.428-21T>A)
c.464T>A (p.Val155Glu)
c.341T>A (p.Val114Glu)
n.479T>A
c.299T>A (p.Val100Glu)
c.239T>A (p.Val80Glu)
18g.62358269T>CCA402613039TNFRSF11Ac.449T>C (p.Val150Ala)
n.367T>C
c.428-21T>C (n.428-21T>C)
c.464T>C (p.Val155Ala)
c.341T>C (p.Val114Ala)
n.479T>C
c.299T>C (p.Val100Ala)
c.239T>C (p.Val80Ala)
18g.62358269T>GCA402613040TNFRSF11Ac.449T>G (p.Val150Gly)
n.367T>G
c.428-21T>G (n.428-21T>G)
c.464T>G (p.Val155Gly)
c.341T>G (p.Val114Gly)
n.479T>G
c.299T>G (p.Val100Gly)
c.239T>G (p.Val80Gly)
18g.62358270G>ACA10604301TNFRSF11Ac.450G>A (p.Val150=)
n.368G>A
c.428-20G>A (n.428-20G>A)
c.465G>A (p.Val155=)
c.342G>A (p.Val114=)
n.480G>A
c.300G>A (p.Val100=)
c.240G>A (p.Val80=)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
18g.62358270G>CCA504077925TNFRSF11Ac.450G>C (p.Val150=)
n.368G>C
c.428-20G>C (n.428-20G>C)
c.465G>C (p.Val155=)
c.342G>C (p.Val114=)
n.480G>C
c.300G>C (p.Val100=)
c.240G>C (p.Val80=)
18g.62358270G=CA2308284517TNFRSF11Ac.450G= (p.Val150=)
n.368G=
c.428-20G= (n.428-20G=)
c.465G= (p.Val155=)
c.342G= (p.Val114=)
n.480G=
c.300G= (p.Val100=)
c.240G= (p.Val80=)
18g.62358270G>TCA504077928TNFRSF11Ac.450G>T (p.Val150=)
n.368G>T
c.428-20G>T (n.428-20G>T)
c.465G>T (p.Val155=)
c.342G>T (p.Val114=)
n.480G>T
c.300G>T (p.Val100=)
c.240G>T (p.Val80=)
 gnomAD v3 gnomAD v4
18g.62358271T>ACA402613041TNFRSF11Ac.451T>A (p.Cys151Ser)
n.369T>A
c.428-19T>A (n.428-19T>A)
c.466T>A (p.Cys156Ser)
c.343T>A (p.Cys115Ser)
n.481T>A
c.301T>A (p.Cys101Ser)
c.241T>A (p.Cys81Ser)
18g.62358271T>CCA402613042TNFRSF11Ac.451T>C (p.Cys151Arg)
n.369T>C
c.428-19T>C (n.428-19T>C)
c.466T>C (p.Cys156Arg)
c.343T>C (p.Cys115Arg)
n.481T>C
c.301T>C (p.Cys101Arg)
c.241T>C (p.Cys81Arg)
18g.62358271T>GCA402613044TNFRSF11Ac.451T>G (p.Cys151Gly)
n.369T>G
c.428-19T>G (n.428-19T>G)
c.466T>G (p.Cys156Gly)
c.343T>G (p.Cys115Gly)
n.481T>G
c.301T>G (p.Cys101Gly)
c.241T>G (p.Cys81Gly)
18g.62358272G>ACA402613050TNFRSF11Ac.452G>A (p.Cys151Tyr)
n.370G>A
c.428-18G>A (n.428-18G>A)
c.467G>A (p.Cys156Tyr)
c.344G>A (p.Cys115Tyr)
n.482G>A
c.302G>A (p.Cys101Tyr)
c.242G>A (p.Cys81Tyr)
 dbSNP gnomAD v3 gnomAD v4
18g.62358272G>CCA402613052TNFRSF11Ac.452G>C (p.Cys151Ser)
n.370G>C
c.428-18G>C (n.428-18G>C)
c.467G>C (p.Cys156Ser)
c.344G>C (p.Cys115Ser)
n.482G>C
c.302G>C (p.Cys101Ser)
c.242G>C (p.Cys81Ser)
18g.62358272G=CA2308284518TNFRSF11Ac.452G= (p.Cys151=)
n.370G=
c.428-18G= (n.428-18G=)
c.467G= (p.Cys156=)
c.344G= (p.Cys115=)
n.482G=
c.302G= (p.Cys101=)
c.242G= (p.Cys81=)
18g.62358272G>TCA402613048TNFRSF11Ac.452G>T (p.Cys151Phe)
n.370G>T
c.428-18G>T (n.428-18G>T)
c.467G>T (p.Cys156Phe)
c.344G>T (p.Cys115Phe)
n.482G>T
c.302G>T (p.Cys101Phe)
c.242G>T (p.Cys81Phe)
 gnomAD v3 gnomAD v4
18g.62358273C>ACA402613055TNFRSF11Ac.453C>A (p.Cys151Ter)
n.371C>A
c.428-17C>A (n.428-17C>A)
c.468C>A (p.Cys156Ter)
c.345C>A (p.Cys115Ter)
n.483C>A
c.303C>A (p.Cys101Ter)
c.243C>A (p.Cys81Ter)
18g.62358273C>GCA402613066TNFRSF11Ac.453C>G (p.Cys151Trp)
n.371C>G
c.428-17C>G (n.428-17C>G)
c.468C>G (p.Cys156Trp)
c.345C>G (p.Cys115Trp)
n.483C>G
c.303C>G (p.Cys101Trp)
c.243C>G (p.Cys81Trp)
 ClinVar
18g.62358273C>TCA504077940TNFRSF11Ac.453C>T (p.Cys151=)
n.371C>T
c.428-17C>T (n.428-17C>T)
c.468C>T (p.Cys156=)
c.345C>T (p.Cys115=)
n.483C>T
c.303C>T (p.Cys101=)
c.243C>T (p.Cys81=)
 gnomAD v3 gnomAD v4
18g.62358274A>CCA402613070TNFRSF11Ac.454A>C (p.Lys152Gln)
n.372A>C
c.428-16A>C (n.428-16A>C)
c.469A>C (p.Lys157Gln)
c.346A>C (p.Lys116Gln)
n.484A>C
c.304A>C (p.Lys102Gln)
c.244A>C (p.Lys82Gln)
18g.62358274A>GCA402613072TNFRSF11Ac.454A>G (p.Lys152Glu)
n.372A>G
c.428-16A>G (n.428-16A>G)
c.469A>G (p.Lys157Glu)
c.346A>G (p.Lys116Glu)
n.484A>G
c.304A>G (p.Lys102Glu)
c.244A>G (p.Lys82Glu)
18g.62358274A>TCA402613074TNFRSF11Ac.454A>T (p.Lys152Ter)
n.372A>T
c.428-16A>T (n.428-16A>T)
c.469A>T (p.Lys157Ter)
c.346A>T (p.Lys116Ter)
n.484A>T
c.304A>T (p.Lys102Ter)
c.244A>T (p.Lys82Ter)
18g.62358275A>CCA402613082TNFRSF11Ac.455A>C (p.Lys152Thr)
n.373A>C
c.428-15A>C (n.428-15A>C)
c.470A>C (p.Lys157Thr)
c.347A>C (p.Lys116Thr)
n.485A>C
c.305A>C (p.Lys102Thr)
c.245A>C (p.Lys82Thr)
18g.62358275A>GCA402613078TNFRSF11Ac.455A>G (p.Lys152Arg)
n.373A>G
c.428-15A>G (n.428-15A>G)
c.470A>G (p.Lys157Arg)
c.347A>G (p.Lys116Arg)
n.485A>G
c.305A>G (p.Lys102Arg)
c.245A>G (p.Lys82Arg)
18g.62358275A>TCA402613080TNFRSF11Ac.455A>T (p.Lys152Ile)
n.373A>T
c.428-15A>T (n.428-15A>T)
c.470A>T (p.Lys157Ile)
c.347A>T (p.Lys116Ile)
n.485A>T
c.305A>T (p.Lys102Ile)
c.245A>T (p.Lys82Ile)
 gnomAD v3 gnomAD v4
18g.62358276A>CCA402613085TNFRSF11Ac.456A>C (p.Lys152Asn)
n.374A>C
c.428-14A>C (n.428-14A>C)
c.471A>C (p.Lys157Asn)
c.348A>C (p.Lys116Asn)
n.486A>C
c.306A>C (p.Lys102Asn)
c.246A>C (p.Lys82Asn)
 gnomAD v4
18g.62358276A>GCA504077948TNFRSF11Ac.456A>G (p.Lys152=)
n.374A>G
c.428-14A>G (n.428-14A>G)
c.471A>G (p.Lys157=)
c.348A>G (p.Lys116=)
n.486A>G
c.306A>G (p.Lys102=)
c.246A>G (p.Lys82=)
18g.62358276A>TCA402613086TNFRSF11Ac.456A>T (p.Lys152Asn)
n.374A>T
c.428-14A>T (n.428-14A>T)
c.471A>T (p.Lys157Asn)
c.348A>T (p.Lys116Asn)
n.486A>T
c.306A>T (p.Lys102Asn)
c.246A>T (p.Lys82Asn)
 gnomAD v4
18g.62358277C>ACA402613087TNFRSF11Ac.457C>A (p.Pro153Thr)
n.375C>A
c.428-13C>A (n.428-13C>A)
c.472C>A (p.Pro158Thr)
c.349C>A (p.Pro117Thr)
n.487C>A
c.307C>A (p.Pro103Thr)
c.247C>A (p.Pro83Thr)
18g.62358277C=CA2308284519TNFRSF11Ac.457C= (p.Pro153=)
n.375C=
c.428-13C= (n.428-13C=)
c.472C= (p.Pro158=)
c.349C= (p.Pro117=)
n.487C=
c.307C= (p.Pro103=)
c.247C= (p.Pro83=)
18g.62358277C>GCA402613088TNFRSF11Ac.457C>G (p.Pro153Ala)
n.375C>G
c.428-13C>G (n.428-13C>G)
c.472C>G (p.Pro158Ala)
c.349C>G (p.Pro117Ala)
n.487C>G
c.307C>G (p.Pro103Ala)
c.247C>G (p.Pro83Ala)
18g.62358277C>TCA8983768TNFRSF11Ac.457C>T (p.Pro153Ser)
n.375C>T
c.428-13C>T (n.428-13C>T)
c.472C>T (p.Pro158Ser)
c.349C>T (p.Pro117Ser)
n.487C>T
c.307C>T (p.Pro103Ser)
c.247C>T (p.Pro83Ser)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
18g.62358278C>ACA402613103TNFRSF11Ac.458C>A (p.Pro153His)
n.376C>A
c.428-12C>A (n.428-12C>A)
c.473C>A (p.Pro158His)
c.350C>A (p.Pro117His)
n.488C>A
c.308C>A (p.Pro103His)
c.248C>A (p.Pro83His)
18g.62358278C>GCA402613100TNFRSF11Ac.458C>G (p.Pro153Arg)
n.376C>G
c.428-12C>G (n.428-12C>G)
c.473C>G (p.Pro158Arg)
c.350C>G (p.Pro117Arg)
n.488C>G
c.308C>G (p.Pro103Arg)
c.248C>G (p.Pro83Arg)
18g.62358278C>TCA402613093TNFRSF11Ac.458C>T (p.Pro153Leu)
n.376C>T
c.428-12C>T (n.428-12C>T)
c.473C>T (p.Pro158Leu)
c.350C>T (p.Pro117Leu)
n.488C>T
c.308C>T (p.Pro103Leu)
c.248C>T (p.Pro83Leu)
18g.62358279T>ACA504077956TNFRSF11Ac.459T>A (p.Pro153=)
n.377T>A
c.428-11T>A (n.428-11T>A)
c.474T>A (p.Pro158=)
c.351T>A (p.Pro117=)
n.489T>A
c.309T>A (p.Pro103=)
c.249T>A (p.Pro83=)
18g.62358279T>CCA504077958TNFRSF11Ac.459T>C (p.Pro153=)
n.377T>C
c.428-11T>C (n.428-11T>C)
c.474T>C (p.Pro158=)
c.351T>C (p.Pro117=)
n.489T>C
c.309T>C (p.Pro103=)
c.249T>C (p.Pro83=)
18g.62358279T>GCA504077959TNFRSF11Ac.459T>G (p.Pro153=)
n.377T>G
c.428-11T>G (n.428-11T>G)
c.474T>G (p.Pro158=)
c.351T>G (p.Pro117=)
n.489T>G
c.309T>G (p.Pro103=)
c.249T>G (p.Pro83=)
18g.62358280T>ACA402613107TNFRSF11Ac.460T>A (p.Cys154Ser)
n.378T>A
c.428-10T>A (n.428-10T>A)
c.475T>A (p.Cys159Ser)
c.352T>A (p.Cys118Ser)
n.490T>A
c.310T>A (p.Cys104Ser)
c.250T>A (p.Cys84Ser)
18g.62358280T>CCA402613111TNFRSF11Ac.460T>C (p.Cys154Arg)
n.378T>C
c.428-10T>C (n.428-10T>C)
c.475T>C (p.Cys159Arg)
c.352T>C (p.Cys118Arg)
n.490T>C
c.310T>C (p.Cys104Arg)
c.250T>C (p.Cys84Arg)
18g.62358280T>GCA402613110TNFRSF11Ac.460T>G (p.Cys154Gly)
n.378T>G
c.428-10T>G (n.428-10T>G)
c.475T>G (p.Cys159Gly)
c.352T>G (p.Cys118Gly)
n.490T>G
c.310T>G (p.Cys104Gly)
c.250T>G (p.Cys84Gly)
18g.62358281G>ACA402613114TNFRSF11Ac.461G>A (p.Cys154Tyr)
n.379G>A
c.428-9G>A (n.428-9G>A)
c.476G>A (p.Cys159Tyr)
c.353G>A (p.Cys118Tyr)
n.491G>A
c.311G>A (p.Cys104Tyr)
c.251G>A (p.Cys84Tyr)
18g.62358281G>CCA402613119TNFRSF11Ac.461G>C (p.Cys154Ser)
n.379G>C
c.428-9G>C (n.428-9G>C)
c.476G>C (p.Cys159Ser)
c.353G>C (p.Cys118Ser)
n.491G>C
c.311G>C (p.Cys104Ser)
c.251G>C (p.Cys84Ser)
18g.62358281G>TCA402613116TNFRSF11Ac.461G>T (p.Cys154Phe)
n.379G>T
c.428-9G>T (n.428-9G>T)
c.476G>T (p.Cys159Phe)
c.353G>T (p.Cys118Phe)
n.491G>T
c.311G>T (p.Cys104Phe)
c.251G>T (p.Cys84Phe)
 gnomAD v4
18g.62358282C>ACA402613122TNFRSF11Ac.462C>A (p.Cys154Ter)
n.380C>A
c.428-8C>A (n.428-8C>A)
c.477C>A (p.Cys159Ter)
c.354C>A (p.Cys118Ter)
n.492C>A
c.312C>A (p.Cys104Ter)
c.252C>A (p.Cys84Ter)
18g.62358282C=CA2308284520TNFRSF11Ac.462C= (p.Cys154=)
n.380C=
c.428-8C= (n.428-8C=)
c.477C= (p.Cys159=)
c.354C= (p.Cys118=)
n.492C=
c.312C= (p.Cys104=)
c.252C= (p.Cys84=)
18g.62358282C>GCA402613125TNFRSF11Ac.462C>G (p.Cys154Trp)
n.380C>G
c.428-8C>G (n.428-8C>G)
c.477C>G (p.Cys159Trp)
c.354C>G (p.Cys118Trp)
n.492C>G
c.312C>G (p.Cys104Trp)
c.252C>G (p.Cys84Trp)
18g.62358282C>TCA504077970TNFRSF11Ac.462C>T (p.Cys154=)
n.380C>T
c.428-8C>T (n.428-8C>T)
c.477C>T (p.Cys159=)
c.354C>T (p.Cys118=)
n.492C>T
c.312C>T (p.Cys104=)
c.252C>T (p.Cys84=)
 dbSNP gnomAD v4
18g.62358283C>ACA402613127TNFRSF11Ac.463C>A (p.Leu155Ile)
n.381C>A
c.428-7C>A (n.428-7C>A)
c.478C>A (p.Leu160Ile)
c.355C>A (p.Leu119Ile)
n.493C>A
c.313C>A (p.Leu105Ile)
c.253C>A (p.Leu85Ile)
18g.62358283C=CA2308284521TNFRSF11Ac.463C= (p.Leu155=)
n.381C=
c.428-7C= (n.428-7C=)
c.478C= (p.Leu160=)
c.355C= (p.Leu119=)
n.493C=
c.313C= (p.Leu105=)
c.253C= (p.Leu85=)
18g.62358283C>GCA402613130TNFRSF11Ac.463C>G (p.Leu155Val)
n.381C>G
c.428-7C>G (n.428-7C>G)
c.478C>G (p.Leu160Val)
c.355C>G (p.Leu119Val)
n.493C>G
c.313C>G (p.Leu105Val)
c.253C>G (p.Leu85Val)
18g.62358283C>TCA8983769TNFRSF11Ac.463C>T (p.Leu155Phe)
n.381C>T
c.428-7C>T (n.428-7C>T)
c.478C>T (p.Leu160Phe)
c.355C>T (p.Leu119Phe)
n.493C>T
c.313C>T (p.Leu105Phe)
c.253C>T (p.Leu85Phe)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
18g.62358284T>ACA402613136TNFRSF11Ac.464T>A (p.Leu155His)
n.382T>A
c.428-6T>A (n.428-6T>A)
c.479T>A (p.Leu160His)
c.356T>A (p.Leu119His)
n.494T>A
c.314T>A (p.Leu105His)
c.254T>A (p.Leu85His)
18g.62358284T>CCA402613138TNFRSF11Ac.464T>C (p.Leu155Pro)
n.382T>C
c.428-6T>C (n.428-6T>C)
c.479T>C (p.Leu160Pro)
c.356T>C (p.Leu119Pro)
n.494T>C
c.314T>C (p.Leu105Pro)
c.254T>C (p.Leu85Pro)
 dbSNP gnomAD v3 gnomAD v4
18g.62358284T>GCA8983770TNFRSF11Ac.464T>G (p.Leu155Arg)
n.382T>G
c.428-6T>G (n.428-6T>G)
c.479T>G (p.Leu160Arg)
c.356T>G (p.Leu119Arg)
n.494T>G
c.314T>G (p.Leu105Arg)
c.254T>G (p.Leu85Arg)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
18g.62358284T=CA2308284522TNFRSF11Ac.464T= (p.Leu155=)
n.382T=
c.428-6T= (n.428-6T=)
c.479T= (p.Leu160=)
c.356T= (p.Leu119=)
n.494T=
c.314T= (p.Leu105=)
c.254T= (p.Leu85=)
18g.62358285T>ACA504077980TNFRSF11Ac.465T>A (p.Leu155=)
n.383T>A
c.428-5T>A (n.428-5T>A)
c.480T>A (p.Leu160=)
c.357T>A (p.Leu119=)
n.495T>A
c.315T>A (p.Leu105=)
c.255T>A (p.Leu85=)
18g.62358285T>CCA504077982TNFRSF11Ac.465T>C (p.Leu155=)
n.383T>C
c.428-5T>C (n.428-5T>C)
c.480T>C (p.Leu160=)
c.357T>C (p.Leu119=)
n.495T>C
c.315T>C (p.Leu105=)
c.255T>C (p.Leu85=)
18g.62358285T>GCA504077984TNFRSF11Ac.465T>G (p.Leu155=)
n.383T>G
c.428-5T>G (n.428-5T>G)
c.480T>G (p.Leu160=)
c.357T>G (p.Leu119=)
n.495T>G
c.315T>G (p.Leu105=)
c.255T>G (p.Leu85=)
18g.62358286G>ACA402613143TNFRSF11Ac.466G>A (p.Ala156Thr)
n.384G>A
c.428-4G>A (n.428-4G>A)
c.481G>A (p.Ala161Thr)
c.358G>A (p.Ala120Thr)
n.496G>A
c.316G>A (p.Ala106Thr)
c.256G>A (p.Ala86Thr)
18g.62358286G>CCA402613145TNFRSF11Ac.466G>C (p.Ala156Pro)
n.384G>C
c.428-4G>C (n.428-4G>C)
c.481G>C (p.Ala161Pro)
c.358G>C (p.Ala120Pro)
n.496G>C
c.316G>C (p.Ala106Pro)
c.256G>C (p.Ala86Pro)
18g.62358286G>TCA402613149TNFRSF11Ac.466G>T (p.Ala156Ser)
n.384G>T
c.428-4G>T (n.428-4G>T)
c.481G>T (p.Ala161Ser)
c.358G>T (p.Ala120Ser)
n.496G>T
c.316G>T (p.Ala106Ser)
c.256G>T (p.Ala86Ser)
 dbSNP gnomAD v3 gnomAD v4
18g.62358287C>ACA402613157TNFRSF11Ac.467C>A (p.Ala156Glu)
n.385C>A
c.428-3C>A (n.428-3C>A)
c.482C>A (p.Ala161Glu)
c.359C>A (p.Ala120Glu)
n.497C>A
c.317C>A (p.Ala106Glu)
c.257C>A (p.Ala86Glu)
18g.62358287C>GCA402613152TNFRSF11Ac.467C>G (p.Ala156Gly)
n.385C>G
c.428-3C>G (n.428-3C>G)
c.482C>G (p.Ala161Gly)
c.359C>G (p.Ala120Gly)
n.497C>G
c.317C>G (p.Ala106Gly)
c.257C>G (p.Ala86Gly)
18g.62358287C>TCA402613155TNFRSF11Ac.467C>T (p.Ala156Val)
n.385C>T
c.428-3C>T (n.428-3C>T)
c.482C>T (p.Ala161Val)
c.359C>T (p.Ala120Val)
n.497C>T
c.317C>T (p.Ala106Val)
c.257C>T (p.Ala86Val)
 dbSNP
18g.62358288A=CA2308284523TNFRSF11Ac.468A= (p.Ala156=)
n.386A=
c.428-2A= (n.428-2A=)
c.483A= (p.Ala161=)
c.360A= (p.Ala120=)
n.498A=
c.318A= (p.Ala106=)
c.258A= (p.Ala86=)
18g.62358288A>CCA8983771TNFRSF11Ac.468A>C (p.Ala156=)
n.386A>C
c.428-2A>C (n.428-2A>C)
c.483A>C (p.Ala161=)
c.360A>C (p.Ala120=)
n.498A>C
c.318A>C (p.Ala106=)
c.258A>C (p.Ala86=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
18g.62358288A>GCA504078000TNFRSF11Ac.468A>G (p.Ala156=)
n.386A>G
c.428-2A>G (n.428-2A>G)
c.483A>G (p.Ala161=)
c.360A>G (p.Ala120=)
n.498A>G
c.318A>G (p.Ala106=)
c.258A>G (p.Ala86=)
 ClinVar
18g.62358288A>TCA504077998TNFRSF11Ac.468A>T (p.Ala156=)
n.386A>T
c.428-2A>T (n.428-2A>T)
c.483A>T (p.Ala161=)
c.360A>T (p.Ala120=)
n.498A>T
c.318A>T (p.Ala106=)
c.258A>T (p.Ala86=)
18g.62358289G>ACA402613160TNFRSF11Ac.469G>A (p.Gly157Ser)
n.387G>A
c.428-1G>A (n.428-1G>A)
c.484G>A (p.Gly162Ser)
c.361G>A (p.Gly121Ser)
n.499G>A
c.319G>A (p.Gly107Ser)
c.259G>A (p.Gly87Ser)
18g.62358289G>CCA402613161TNFRSF11Ac.469G>C (p.Gly157Arg)
n.387G>C
c.428-1G>C (n.428-1G>C)
c.484G>C (p.Gly162Arg)
c.361G>C (p.Gly121Arg)
n.499G>C
c.319G>C (p.Gly107Arg)
c.259G>C (p.Gly87Arg)
18g.62358289G>TCA402613164TNFRSF11Ac.469G>T (p.Gly157Cys)
n.387G>T
c.428-1G>T (n.428-1G>T)
c.484G>T (p.Gly162Cys)
c.361G>T (p.Gly121Cys)
n.499G>T
c.319G>T (p.Gly107Cys)
c.259G>T (p.Gly87Cys)
 gnomAD v4
18g.62358290G>ACA402613166TNFRSF11Ac.470G>A (p.Gly157Asp)
n.388G>A
c.428G>A (p.Cys143Tyr)
c.485G>A (p.Gly162Asp)
c.362G>A (p.Gly121Asp)
n.500G>A
c.320G>A (p.Gly107Asp)
c.260G>A (p.Gly87Asp)
 dbSNP gnomAD v3 gnomAD v4
18g.62358290G>CCA402613170TNFRSF11Ac.470G>C (p.Gly157Ala)
n.388G>C
c.428G>C (p.Cys143Ser)
c.485G>C (p.Gly162Ala)
c.362G>C (p.Gly121Ala)
n.500G>C
c.320G>C (p.Gly107Ala)
c.260G>C (p.Gly87Ala)
18g.62358290G=CA2308284524TNFRSF11Ac.470G= (p.Gly157=)
n.388G=
c.428G= (p.Cys143=)
c.485G= (p.Gly162=)
c.362G= (p.Gly121=)
n.500G=
c.320G= (p.Gly107=)
c.260G= (p.Gly87=)
18g.62358290G>TCA402613172TNFRSF11Ac.470G>T (p.Gly157Val)
n.388G>T
c.428G>T (p.Cys143Phe)
c.485G>T (p.Gly162Val)
c.362G>T (p.Gly121Val)
n.500G>T
c.320G>T (p.Gly107Val)
c.260G>T (p.Gly87Val)
 gnomAD v4
18g.62358291C>ACA504078011TNFRSF11Ac.471C>A (p.Gly157=)
n.389C>A
c.429C>A (p.Cys143Ter)
c.486C>A (p.Gly162=)
c.363C>A (p.Gly121=)
n.501C>A
c.321C>A (p.Gly107=)
c.261C>A (p.Gly87=)
18g.62358291C>GCA504078015TNFRSF11Ac.471C>G (p.Gly157=)
n.389C>G
c.429C>G (p.Cys143Trp)
c.486C>G (p.Gly162=)
c.363C>G (p.Gly121=)
n.501C>G
c.321C>G (p.Gly107=)
c.261C>G (p.Gly87=)
18g.62358291C>TCA504078017TNFRSF11Ac.471C>T (p.Gly157=)
n.389C>T
c.429C>T (p.Cys143=)
c.486C>T (p.Gly162=)
c.363C>T (p.Gly121=)
n.501C>T
c.321C>T (p.Gly107=)
c.261C>T (p.Gly87=)
18g.62358292T>ACA402613176TNFRSF11Ac.472T>A (p.Tyr158Asn)
n.390T>A
c.430T>A (p.Tyr144Asn)
c.487T>A (p.Tyr163Asn)
c.364T>A (p.Tyr122Asn)
n.502T>A
c.322T>A (p.Tyr108Asn)
c.262T>A (p.Tyr88Asn)
18g.62358292T>CCA402613178TNFRSF11Ac.472T>C (p.Tyr158His)
n.390T>C
c.430T>C (p.Tyr144His)
c.487T>C (p.Tyr163His)
c.364T>C (p.Tyr122His)
n.502T>C
c.322T>C (p.Tyr108His)
c.262T>C (p.Tyr88His)
 gnomAD v4
18g.62358292T>GCA402613180TNFRSF11Ac.472T>G (p.Tyr158Asp)
n.390T>G
c.430T>G (p.Tyr144Asp)
c.487T>G (p.Tyr163Asp)
c.364T>G (p.Tyr122Asp)
n.502T>G
c.322T>G (p.Tyr108Asp)
c.262T>G (p.Tyr88Asp)
18g.62358293A>CCA402613188TNFRSF11Ac.473A>C (p.Tyr158Ser)
n.391A>C
c.431A>C (p.Tyr144Ser)
c.488A>C (p.Tyr163Ser)
c.365A>C (p.Tyr122Ser)
n.503A>C
c.323A>C (p.Tyr108Ser)
c.263A>C (p.Tyr88Ser)
18g.62358293A>GCA402613190TNFRSF11Ac.473A>G (p.Tyr158Cys)
n.391A>G
c.431A>G (p.Tyr144Cys)
c.488A>G (p.Tyr163Cys)
c.365A>G (p.Tyr122Cys)
n.503A>G
c.323A>G (p.Tyr108Cys)
c.263A>G (p.Tyr88Cys)
18g.62358293A>TCA402613186TNFRSF11Ac.473A>T (p.Tyr158Phe)
n.391A>T
c.431A>T (p.Tyr144Phe)
c.488A>T (p.Tyr163Phe)
c.365A>T (p.Tyr122Phe)
n.503A>T
c.323A>T (p.Tyr108Phe)
c.263A>T (p.Tyr88Phe)
18g.62358294C>ACA402613192TNFRSF11Ac.474C>A (p.Tyr158Ter)
n.392C>A
c.432C>A (p.Tyr144Ter)
c.489C>A (p.Tyr163Ter)
c.366C>A (p.Tyr122Ter)
n.504C>A
c.324C>A (p.Tyr108Ter)
c.264C>A (p.Tyr88Ter)
18g.62358294C>GCA402613195TNFRSF11Ac.474C>G (p.Tyr158Ter)
n.392C>G
c.432C>G (p.Tyr144Ter)
c.489C>G (p.Tyr163Ter)
c.366C>G (p.Tyr122Ter)
n.504C>G
c.324C>G (p.Tyr108Ter)
c.264C>G (p.Tyr88Ter)
18g.62358294C>TCA504078030TNFRSF11Ac.474C>T (p.Tyr158=)
n.392C>T
c.432C>T (p.Tyr144=)
c.489C>T (p.Tyr163=)
c.366C>T (p.Tyr122=)
n.504C>T
c.324C>T (p.Tyr108=)
c.264C>T (p.Tyr88=)
18g.62358295T>ACA402613198TNFRSF11Ac.475T>A (p.Phe159Ile)
n.393T>A
c.433T>A (p.Phe145Ile)
c.490T>A (p.Phe164Ile)
c.367T>A (p.Phe123Ile)
n.505T>A
c.325T>A (p.Phe109Ile)
c.265T>A (p.Phe89Ile)
18g.62358295T>CCA402613200TNFRSF11Ac.475T>C (p.Phe159Leu)
n.393T>C
c.433T>C (p.Phe145Leu)
c.490T>C (p.Phe164Leu)
c.367T>C (p.Phe123Leu)
n.505T>C
c.325T>C (p.Phe109Leu)
c.265T>C (p.Phe89Leu)
18g.62358295T>GCA402613213TNFRSF11Ac.475T>G (p.Phe159Val)
n.393T>G
c.433T>G (p.Phe145Val)
c.490T>G (p.Phe164Val)
c.367T>G (p.Phe123Val)
n.505T>G
c.325T>G (p.Phe109Val)
c.265T>G (p.Phe89Val)
18g.62358296T>ACA402613216TNFRSF11Ac.476T>A (p.Phe159Tyr)
n.394T>A
c.434T>A (p.Phe145Tyr)
c.491T>A (p.Phe164Tyr)
c.368T>A (p.Phe123Tyr)
n.506T>A
c.326T>A (p.Phe109Tyr)
c.266T>A (p.Phe89Tyr)
18g.62358296T>CCA402613214TNFRSF11Ac.476T>C (p.Phe159Ser)
n.394T>C
c.434T>C (p.Phe145Ser)
c.491T>C (p.Phe164Ser)
c.368T>C (p.Phe123Ser)
n.506T>C
c.326T>C (p.Phe109Ser)
c.266T>C (p.Phe89Ser)
18g.62358296T>GCA402613215TNFRSF11Ac.476T>G (p.Phe159Cys)
n.394T>G
c.434T>G (p.Phe145Cys)
c.491T>G (p.Phe164Cys)
c.368T>G (p.Phe123Cys)
n.506T>G
c.326T>G (p.Phe109Cys)
c.266T>G (p.Phe89Cys)
18g.62358297C>ACA402613218TNFRSF11Ac.477C>A (p.Phe159Leu)
n.395C>A
c.435C>A (p.Phe145Leu)
c.492C>A (p.Phe164Leu)
c.369C>A (p.Phe123Leu)
n.507C>A
c.327C>A (p.Phe109Leu)
c.267C>A (p.Phe89Leu)
18g.62358297C>GCA402613227TNFRSF11Ac.477C>G (p.Phe159Leu)
n.395C>G
c.435C>G (p.Phe145Leu)
c.492C>G (p.Phe164Leu)
c.369C>G (p.Phe123Leu)
n.507C>G
c.327C>G (p.Phe109Leu)
c.267C>G (p.Phe89Leu)
18g.62358297C>TCA504078047TNFRSF11Ac.477C>T (p.Phe159=)
n.395C>T
c.435C>T (p.Phe145=)
c.492C>T (p.Phe164=)
c.369C>T (p.Phe123=)
n.507C>T
c.327C>T (p.Phe109=)
c.267C>T (p.Phe89=)
18g.62358298T>ACA402613231TNFRSF11Ac.478T>A (p.Ser160Thr)
n.396T>A
c.436T>A (p.Ser146Thr)
c.493T>A (p.Ser165Thr)
c.370T>A (p.Ser124Thr)
n.508T>A
c.328T>A (p.Ser110Thr)
c.268T>A (p.Ser90Thr)
18g.62358298T>CCA402613233TNFRSF11Ac.478T>C (p.Ser160Pro)
n.396T>C
c.436T>C (p.Ser146Pro)
c.493T>C (p.Ser165Pro)
c.370T>C (p.Ser124Pro)
n.508T>C
c.328T>C (p.Ser110Pro)
c.268T>C (p.Ser90Pro)
18g.62358298T>GCA402613240TNFRSF11Ac.478T>G (p.Ser160Ala)
n.396T>G
c.436T>G (p.Ser146Ala)
c.493T>G (p.Ser165Ala)
c.370T>G (p.Ser124Ala)
n.508T>G
c.328T>G (p.Ser110Ala)
c.268T>G (p.Ser90Ala)
18g.62358299C>ACA402613242TNFRSF11Ac.479C>A (p.Ser160Tyr)
n.397C>A
c.437C>A (p.Ser146Tyr)
c.494C>A (p.Ser165Tyr)
c.371C>A (p.Ser124Tyr)
n.509C>A
c.329C>A (p.Ser110Tyr)
c.269C>A (p.Ser90Tyr)
18g.62358299C>GCA402613249TNFRSF11Ac.479C>G (p.Ser160Cys)
n.397C>G
c.437C>G (p.Ser146Cys)
c.494C>G (p.Ser165Cys)
c.371C>G (p.Ser124Cys)
n.509C>G
c.329C>G (p.Ser110Cys)
c.269C>G (p.Ser90Cys)
 gnomAD v4
18g.62358299C>TCA402613246TNFRSF11Ac.479C>T (p.Ser160Phe)
n.397C>T
c.437C>T (p.Ser146Phe)
c.494C>T (p.Ser165Phe)
c.371C>T (p.Ser124Phe)
n.509C>T
c.329C>T (p.Ser110Phe)
c.269C>T (p.Ser90Phe)
18g.62358300T>ACA504078060TNFRSF11Ac.480T>A (p.Ser160=)
n.398T>A
c.438T>A (p.Ser146=)
c.495T>A (p.Ser165=)
c.372T>A (p.Ser124=)
n.510T>A
c.330T>A (p.Ser110=)
c.270T>A (p.Ser90=)
18g.62358300T>CCA504078061TNFRSF11Ac.480T>C (p.Ser160=)
n.398T>C
c.438T>C (p.Ser146=)
c.495T>C (p.Ser165=)
c.372T>C (p.Ser124=)
n.510T>C
c.330T>C (p.Ser110=)
c.270T>C (p.Ser90=)
18g.62358300T>GCA504078062TNFRSF11Ac.480T>G (p.Ser160=)
n.398T>G
c.438T>G (p.Ser146=)
c.495T>G (p.Ser165=)
c.372T>G (p.Ser124=)
n.510T>G
c.330T>G (p.Ser110=)
c.270T>G (p.Ser90=)
18g.62358301G>ACA402613252TNFRSF11Ac.481G>A (p.Asp161Asn)
n.399G>A
c.439G>A (p.Asp147Asn)
c.496G>A (p.Asp166Asn)
c.373G>A (p.Asp125Asn)
n.511G>A
c.331G>A (p.Asp111Asn)
c.271G>A (p.Asp91Asn)
 ClinVar gnomAD v4
18g.62358301G>CCA402613254TNFRSF11Ac.481G>C (p.Asp161His)
n.399G>C
c.439G>C (p.Asp147His)
c.496G>C (p.Asp166His)
c.373G>C (p.Asp125His)
n.511G>C
c.331G>C (p.Asp111His)
c.271G>C (p.Asp91His)
18g.62358301G>TCA402613258TNFRSF11Ac.481G>T (p.Asp161Tyr)
n.399G>T
c.439G>T (p.Asp147Tyr)
c.496G>T (p.Asp166Tyr)
c.373G>T (p.Asp125Tyr)
n.511G>T
c.331G>T (p.Asp111Tyr)
c.271G>T (p.Asp91Tyr)
 gnomAD v4
18g.62358302A>CCA402613260TNFRSF11Ac.482A>C (p.Asp161Ala)
n.400A>C
c.440A>C (p.Asp147Ala)
c.497A>C (p.Asp166Ala)
c.374A>C (p.Asp125Ala)
n.512A>C
c.332A>C (p.Asp111Ala)
c.272A>C (p.Asp91Ala)
18g.62358302A>GCA402613263TNFRSF11Ac.482A>G (p.Asp161Gly)
n.400A>G
c.440A>G (p.Asp147Gly)
c.497A>G (p.Asp166Gly)
c.374A>G (p.Asp125Gly)
n.512A>G
c.332A>G (p.Asp111Gly)
c.272A>G (p.Asp91Gly)
18g.62358302A>TCA402613267TNFRSF11Ac.482A>T (p.Asp161Val)
n.400A>T
c.440A>T (p.Asp147Val)
c.497A>T (p.Asp166Val)
c.374A>T (p.Asp125Val)
n.512A>T
c.332A>T (p.Asp111Val)
c.272A>T (p.Asp91Val)
18g.62358303T>ACA402613269TNFRSF11Ac.483T>A (p.Asp161Glu)
n.401T>A
c.441T>A (p.Asp147Glu)
c.498T>A (p.Asp166Glu)
c.375T>A (p.Asp125Glu)
n.513T>A
c.333T>A (p.Asp111Glu)
c.273T>A (p.Asp91Glu)
18g.62358303T>CCA504078074TNFRSF11Ac.483T>C (p.Asp161=)
n.401T>C
c.441T>C (p.Asp147=)
c.498T>C (p.Asp166=)
c.375T>C (p.Asp125=)
n.513T>C
c.333T>C (p.Asp111=)
c.273T>C (p.Asp91=)
18g.62358303T>GCA402613270TNFRSF11Ac.483T>G (p.Asp161Glu)
n.401T>G
c.441T>G (p.Asp147Glu)
c.498T>G (p.Asp166Glu)
c.375T>G (p.Asp125Glu)
n.513T>G
c.333T>G (p.Asp111Glu)
c.273T>G (p.Asp91Glu)
 ClinVar
18g.62358304G>ACA402613277TNFRSF11Ac.484G>A (p.Ala162Thr)
n.402G>A
c.442G>A (p.Ala148Thr)
c.499G>A (p.Ala167Thr)
c.376G>A (p.Ala126Thr)
n.514G>A
c.334G>A (p.Ala112Thr)
c.274G>A (p.Ala92Thr)
18g.62358304G>CCA402613278TNFRSF11Ac.484G>C (p.Ala162Pro)
n.402G>C
c.442G>C (p.Ala148Pro)
c.499G>C (p.Ala167Pro)
c.376G>C (p.Ala126Pro)
n.514G>C
c.334G>C (p.Ala112Pro)
c.274G>C (p.Ala92Pro)
18g.62358304G>TCA402613279TNFRSF11Ac.484G>T (p.Ala162Ser)
n.402G>T
c.442G>T (p.Ala148Ser)
c.499G>T (p.Ala167Ser)
c.376G>T (p.Ala126Ser)
n.514G>T
c.334G>T (p.Ala112Ser)
c.274G>T (p.Ala92Ser)
 gnomAD v4
18g.62358305C>ACA402613284TNFRSF11Ac.485C>A (p.Ala162Asp)
n.403C>A
c.443C>A (p.Ala148Asp)
c.500C>A (p.Ala167Asp)
c.377C>A (p.Ala126Asp)
n.515C>A
c.335C>A (p.Ala112Asp)
c.275C>A (p.Ala92Asp)
 gnomAD v4
18g.62358305C>GCA402613281TNFRSF11Ac.485C>G (p.Ala162Gly)
n.403C>G
c.443C>G (p.Ala148Gly)
c.500C>G (p.Ala167Gly)
c.377C>G (p.Ala126Gly)
n.515C>G
c.335C>G (p.Ala112Gly)
c.275C>G (p.Ala92Gly)
18g.62358305C>TCA402613280TNFRSF11Ac.485C>T (p.Ala162Val)
n.403C>T
c.443C>T (p.Ala148Val)
c.500C>T (p.Ala167Val)
c.377C>T (p.Ala126Val)
n.515C>T
c.335C>T (p.Ala112Val)
c.275C>T (p.Ala92Val)
 gnomAD v4
18g.62358306C>ACA504078087TNFRSF11Ac.486C>A (p.Ala162=)
n.404C>A
c.444C>A (p.Ala148=)
c.501C>A (p.Ala167=)
c.378C>A (p.Ala126=)
n.516C>A
c.336C>A (p.Ala112=)
c.276C>A (p.Ala92=)
18g.62358306C=CA2308284525TNFRSF11Ac.486C= (p.Ala162=)
n.404C=
c.444C= (p.Ala148=)
c.501C= (p.Ala167=)
c.378C= (p.Ala126=)
n.516C=
c.336C= (p.Ala112=)
c.276C= (p.Ala92=)
18g.62358306C>GCA504078089TNFRSF11Ac.486C>G (p.Ala162=)
n.404C>G
c.444C>G (p.Ala148=)
c.501C>G (p.Ala167=)
c.378C>G (p.Ala126=)
n.516C>G
c.336C>G (p.Ala112=)
c.276C>G (p.Ala92=)
 gnomAD v4
18g.62358306C>TCA8983772TNFRSF11Ac.486C>T (p.Ala162=)
n.404C>T
c.444C>T (p.Ala148=)
c.501C>T (p.Ala167=)
c.378C>T (p.Ala126=)
n.516C>T
c.336C>T (p.Ala112=)
c.276C>T (p.Ala92=)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
18g.62358307T>ACA402613292TNFRSF11Ac.487T>A (p.Phe163Ile)
n.405T>A
c.445T>A (p.Phe149Ile)
c.502T>A (p.Phe168Ile)
c.379T>A (p.Phe127Ile)
n.517T>A
c.337T>A (p.Phe113Ile)
c.277T>A (p.Phe93Ile)
18g.62358307T>CCA402613288TNFRSF11Ac.487T>C (p.Phe163Leu)
n.405T>C
c.445T>C (p.Phe149Leu)
c.502T>C (p.Phe168Leu)
c.379T>C (p.Phe127Leu)
n.517T>C
c.337T>C (p.Phe113Leu)
c.277T>C (p.Phe93Leu)
18g.62358307T>GCA402613290TNFRSF11Ac.487T>G (p.Phe163Val)
n.405T>G
c.445T>G (p.Phe149Val)
c.502T>G (p.Phe168Val)
c.379T>G (p.Phe127Val)
n.517T>G
c.337T>G (p.Phe113Val)
c.277T>G (p.Phe93Val)
18g.62358310delCA2642068203TNFRSF11Ac.490del (p.Ser164ProfsTer19)
n.408del
c.448del (p.Ser150ProfsTer19)
c.505del (p.Ser169ProfsTer19)
c.382del (p.Ser128ProfsTer19)
n.520del
c.340del (p.Ser114ProfsTer19)
c.280del (p.Ser94ProfsTer19)
 gnomAD v4
18g.62358308T>ACA402613297TNFRSF11Ac.488T>A (p.Phe163Tyr)
n.406T>A
c.446T>A (p.Phe149Tyr)
c.503T>A (p.Phe168Tyr)
c.380T>A (p.Phe127Tyr)
n.518T>A
c.338T>A (p.Phe113Tyr)
c.278T>A (p.Phe93Tyr)
18g.62358308T>CCA402613300TNFRSF11Ac.488T>C (p.Phe163Ser)
n.406T>C
c.446T>C (p.Phe149Ser)
c.503T>C (p.Phe168Ser)
c.380T>C (p.Phe127Ser)
n.518T>C
c.338T>C (p.Phe113Ser)
c.278T>C (p.Phe93Ser)
18g.62358308T>GCA8983773TNFRSF11Ac.488T>G (p.Phe163Cys)
n.406T>G
c.446T>G (p.Phe149Cys)
c.503T>G (p.Phe168Cys)
c.380T>G (p.Phe127Cys)
n.518T>G
c.338T>G (p.Phe113Cys)
c.278T>G (p.Phe93Cys)
 dbSNP ExAC gnomAD v2 gnomAD v4
18g.62358308T=CA2308284526TNFRSF11Ac.488T= (p.Phe163=)
n.406T=
c.446T= (p.Phe149=)
c.503T= (p.Phe168=)
c.380T= (p.Phe127=)
n.518T=
c.338T= (p.Phe113=)
c.278T= (p.Phe93=)
18g.62358309T>ACA402613306TNFRSF11Ac.489T>A (p.Phe163Leu)
n.407T>A
c.447T>A (p.Phe149Leu)
c.504T>A (p.Phe168Leu)
c.381T>A (p.Phe127Leu)
n.519T>A
c.339T>A (p.Phe113Leu)
c.279T>A (p.Phe93Leu)
18g.62358309T>CCA504078103TNFRSF11Ac.489T>C (p.Phe163=)
n.407T>C
c.447T>C (p.Phe149=)
c.504T>C (p.Phe168=)
c.381T>C (p.Phe127=)
n.519T>C
c.339T>C (p.Phe113=)
c.279T>C (p.Phe93=)
18g.62358309T>GCA402613307TNFRSF11Ac.489T>G (p.Phe163Leu)
n.407T>G
c.447T>G (p.Phe149Leu)
c.504T>G (p.Phe168Leu)
c.381T>G (p.Phe127Leu)
n.519T>G
c.339T>G (p.Phe113Leu)
c.279T>G (p.Phe93Leu)
18g.62358310T>ACA402613308TNFRSF11Ac.490T>A (p.Ser164Thr)
n.408T>A
c.448T>A (p.Ser150Thr)
c.505T>A (p.Ser169Thr)
c.382T>A (p.Ser128Thr)
n.520T>A
c.340T>A (p.Ser114Thr)
c.280T>A (p.Ser94Thr)
18g.62358310T>CCA402613309TNFRSF11Ac.490T>C (p.Ser164Pro)
n.408T>C
c.448T>C (p.Ser150Pro)
c.505T>C (p.Ser169Pro)
c.382T>C (p.Ser128Pro)
n.520T>C
c.340T>C (p.Ser114Pro)
c.280T>C (p.Ser94Pro)
18g.62358310T>GCA402613310TNFRSF11Ac.490T>G (p.Ser164Ala)
n.408T>G
c.448T>G (p.Ser150Ala)
c.505T>G (p.Ser169Ala)
c.382T>G (p.Ser128Ala)
n.520T>G
c.340T>G (p.Ser114Ala)
c.280T>G (p.Ser94Ala)
18g.62358311C>ACA402613312TNFRSF11Ac.491C>A (p.Ser164Tyr)
n.409C>A
c.449C>A (p.Ser150Tyr)
c.506C>A (p.Ser169Tyr)
c.383C>A (p.Ser128Tyr)
n.521C>A
c.341C>A (p.Ser114Tyr)
c.281C>A (p.Ser94Tyr)
18g.62358311C>GCA402613313TNFRSF11Ac.491C>G (p.Ser164Cys)
n.409C>G
c.449C>G (p.Ser150Cys)
c.506C>G (p.Ser169Cys)
c.383C>G (p.Ser128Cys)
n.521C>G
c.341C>G (p.Ser114Cys)
c.281C>G (p.Ser94Cys)
18g.62358311C>TCA402613315TNFRSF11Ac.491C>T (p.Ser164Phe)
n.409C>T
c.449C>T (p.Ser150Phe)
c.506C>T (p.Ser169Phe)
c.383C>T (p.Ser128Phe)
n.521C>T
c.341C>T (p.Ser114Phe)
c.281C>T (p.Ser94Phe)
 gnomAD v4 COSMIC
18g.62358312C>ACA504078117TNFRSF11Ac.492C>A (p.Ser164=)
n.410C>A
c.450C>A (p.Ser150=)
c.507C>A (p.Ser169=)
c.384C>A (p.Ser128=)
n.522C>A
c.342C>A (p.Ser114=)
c.282C>A (p.Ser94=)
18g.62358312C=CA2308284527TNFRSF11Ac.492C= (p.Ser164=)
n.410C=
c.450C= (p.Ser150=)
c.507C= (p.Ser169=)
c.384C= (p.Ser128=)
n.522C=
c.342C= (p.Ser114=)
c.282C= (p.Ser94=)
18g.62358312C>GCA504078114TNFRSF11Ac.492C>G (p.Ser164=)
n.410C>G
c.450C>G (p.Ser150=)
c.507C>G (p.Ser169=)
c.384C>G (p.Ser128=)
n.522C>G
c.342C>G (p.Ser114=)
c.282C>G (p.Ser94=)
18g.62358312C>TCA504078112TNFRSF11Ac.492C>T (p.Ser164=)
n.410C>T
c.450C>T (p.Ser150=)
c.507C>T (p.Ser169=)
c.384C>T (p.Ser128=)
n.522C>T
c.342C>T (p.Ser114=)
c.282C>T (p.Ser94=)
 dbSNP gnomAD v4
18g.62358313T>ACA402613323TNFRSF11Ac.493T>A (p.Ser165Thr)
n.411T>A
c.451T>A (p.Ser151Thr)
c.508T>A (p.Ser170Thr)
c.385T>A (p.Ser129Thr)
n.523T>A
c.343T>A (p.Ser115Thr)
c.283T>A (p.Ser95Thr)
18g.62358313T>CCA402613317TNFRSF11Ac.493T>C (p.Ser165Pro)
n.411T>C
c.451T>C (p.Ser151Pro)
c.508T>C (p.Ser170Pro)
c.385T>C (p.Ser129Pro)
n.523T>C
c.343T>C (p.Ser115Pro)
c.283T>C (p.Ser95Pro)
 dbSNP gnomAD v4
18g.62358313T>GCA402613319TNFRSF11Ac.493T>G (p.Ser165Ala)
n.411T>G
c.451T>G (p.Ser151Ala)
c.508T>G (p.Ser170Ala)
c.385T>G (p.Ser129Ala)
n.523T>G
c.343T>G (p.Ser115Ala)
c.283T>G (p.Ser95Ala)
 dbSNP gnomAD v2 gnomAD v4
18g.62358313T=CA2308284528TNFRSF11Ac.493T= (p.Ser165=)
n.411T=
c.451T= (p.Ser151=)
c.508T= (p.Ser170=)
c.385T= (p.Ser129=)
n.523T=
c.343T= (p.Ser115=)
c.283T= (p.Ser95=)
18g.62358314C>ACA402613326TNFRSF11Ac.494C>A (p.Ser165Tyr)
n.412C>A
c.452C>A (p.Ser151Tyr)
c.509C>A (p.Ser170Tyr)
c.386C>A (p.Ser129Tyr)
n.524C>A
c.344C>A (p.Ser115Tyr)
c.284C>A (p.Ser95Tyr)
18g.62358314C>GCA402613329TNFRSF11Ac.494C>G (p.Ser165Cys)
n.412C>G
c.452C>G (p.Ser151Cys)
c.509C>G (p.Ser170Cys)
c.386C>G (p.Ser129Cys)
n.524C>G
c.344C>G (p.Ser115Cys)
c.284C>G (p.Ser95Cys)
18g.62358314C>TCA402613331TNFRSF11Ac.494C>T (p.Ser165Phe)
n.412C>T
c.452C>T (p.Ser151Phe)
c.509C>T (p.Ser170Phe)
c.386C>T (p.Ser129Phe)
n.524C>T
c.344C>T (p.Ser115Phe)
c.284C>T (p.Ser95Phe)
 COSMIC
18g.62358315C>ACA8983774TNFRSF11Ac.495C>A (p.Ser165=)
n.413C>A
c.453C>A (p.Ser151=)
c.510C>A (p.Ser170=)
c.387C>A (p.Ser129=)
n.525C>A
c.345C>A (p.Ser115=)
c.285C>A (p.Ser95=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
18g.62358315C=CA2308284529TNFRSF11Ac.495C= (p.Ser165=)
n.413C=
c.453C= (p.Ser151=)
c.510C= (p.Ser170=)
c.387C= (p.Ser129=)
n.525C=
c.345C= (p.Ser115=)
c.285C= (p.Ser95=)
18g.62358315C>GCA504078130TNFRSF11Ac.495C>G (p.Ser165=)
n.413C>G
c.453C>G (p.Ser151=)
c.510C>G (p.Ser170=)
c.387C>G (p.Ser129=)
n.525C>G
c.345C>G (p.Ser115=)
c.285C>G (p.Ser95=)
18g.62358315C>TCA504078128TNFRSF11Ac.495C>T (p.Ser165=)
n.413C>T
c.453C>T (p.Ser151=)
c.510C>T (p.Ser170=)
c.387C>T (p.Ser129=)
n.525C>T
c.345C>T (p.Ser115=)
c.285C>T (p.Ser95=)
18g.62358316A>CCA402613337TNFRSF11Ac.496A>C (p.Thr166Pro)
n.414A>C
c.454A>C (p.Thr152Pro)
c.511A>C (p.Thr171Pro)
c.388A>C (p.Thr130Pro)
n.526A>C
c.346A>C (p.Thr116Pro)
c.286A>C (p.Thr96Pro)
18g.62358316A>GCA402613339TNFRSF11Ac.496A>G (p.Thr166Ala)
n.414A>G
c.454A>G (p.Thr152Ala)
c.511A>G (p.Thr171Ala)
c.388A>G (p.Thr130Ala)
n.526A>G
c.346A>G (p.Thr116Ala)
c.286A>G (p.Thr96Ala)
18g.62358316A>TCA402613342TNFRSF11Ac.496A>T (p.Thr166Ser)
n.414A>T
c.454A>T (p.Thr152Ser)
c.511A>T (p.Thr171Ser)
c.388A>T (p.Thr130Ser)
n.526A>T
c.346A>T (p.Thr116Ser)
c.286A>T (p.Thr96Ser)
18g.62358317C>ACA402613345TNFRSF11Ac.497C>A (p.Thr166Lys)
n.415C>A
c.455C>A (p.Thr152Lys)
c.512C>A (p.Thr171Lys)
c.389C>A (p.Thr130Lys)
n.527C>A
c.347C>A (p.Thr116Lys)
c.287C>A (p.Thr96Lys)
 gnomAD v4
18g.62358317C=CA2308284530TNFRSF11Ac.497C= (p.Thr166=)
n.415C=
c.455C= (p.Thr152=)
c.512C= (p.Thr171=)
c.389C= (p.Thr130=)
n.527C=
c.347C= (p.Thr116=)
c.287C= (p.Thr96=)
18g.62358317C>GCA402613346TNFRSF11Ac.497C>G (p.Thr166Arg)
n.415C>G
c.455C>G (p.Thr152Arg)
c.512C>G (p.Thr171Arg)
c.389C>G (p.Thr130Arg)
n.527C>G
c.347C>G (p.Thr116Arg)
c.287C>G (p.Thr96Arg)
18g.62358317C>TCA8983775TNFRSF11Ac.497C>T (p.Thr166Met)
n.415C>T
c.455C>T (p.Thr152Met)
c.512C>T (p.Thr171Met)
c.389C>T (p.Thr130Met)
n.527C>T
c.347C>T (p.Thr116Met)
c.287C>T (p.Thr96Met)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
18g.62358318G>ACA8983776TNFRSF11Ac.498G>A (p.Thr166=)
n.416G>A
c.456G>A (p.Thr152=)
c.513G>A (p.Thr171=)
c.390G>A (p.Thr130=)
n.528G>A
c.348G>A (p.Thr116=)
c.288G>A (p.Thr96=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
18g.62358318G>CCA504078145TNFRSF11Ac.498G>C (p.Thr166=)
n.416G>C
c.456G>C (p.Thr152=)
c.513G>C (p.Thr171=)
c.390G>C (p.Thr130=)
n.528G>C
c.348G>C (p.Thr116=)
c.288G>C (p.Thr96=)
 ClinVar dbSNP
18g.62358318G=CA2308284531TNFRSF11Ac.498G= (p.Thr166=)
n.416G=
c.456G= (p.Thr152=)
c.513G= (p.Thr171=)
c.390G= (p.Thr130=)
n.528G=
c.348G= (p.Thr116=)
c.288G= (p.Thr96=)
18g.62358318G>TCA504078147TNFRSF11Ac.498G>T (p.Thr166=)
n.416G>T
c.456G>T (p.Thr152=)
c.513G>T (p.Thr171=)
c.390G>T (p.Thr130=)
n.528G>T
c.348G>T (p.Thr116=)
c.288G>T (p.Thr96=)
18g.62358319G>ACA301696818TNFRSF11Ac.499G>A (p.Asp167Asn)
n.417G>A
c.457G>A (p.Asp153Asn)
c.514G>A (p.Asp172Asn)
c.391G>A (p.Asp131Asn)
n.529G>A
c.349G>A (p.Asp117Asn)
c.289G>A (p.Asp97Asn)
 dbSNP gnomAD v2 gnomAD v4
18g.62358319G>CCA402613355TNFRSF11Ac.499G>C (p.Asp167His)
n.417G>C
c.457G>C (p.Asp153His)
c.514G>C (p.Asp172His)
c.391G>C (p.Asp131His)
n.529G>C
c.349G>C (p.Asp117His)
c.289G>C (p.Asp97His)
18g.62358319G=CA2308284532TNFRSF11Ac.499G= (p.Asp167=)
n.417G=
c.457G= (p.Asp153=)
c.514G= (p.Asp172=)
c.391G= (p.Asp131=)
n.529G=
c.349G= (p.Asp117=)
c.289G= (p.Asp97=)
18g.62358319G>TCA402613353TNFRSF11Ac.499G>T (p.Asp167Tyr)
n.417G>T
c.457G>T (p.Asp153Tyr)
c.514G>T (p.Asp172Tyr)
c.391G>T (p.Asp131Tyr)
n.529G>T
c.349G>T (p.Asp117Tyr)
c.289G>T (p.Asp97Tyr)
18g.62358320A=CA2308284533TNFRSF11Ac.500A= (p.Asp167=)
n.418A=
c.458A= (p.Asp153=)
c.515A= (p.Asp172=)
c.392A= (p.Asp131=)
n.530A=
c.350A= (p.Asp117=)
c.290A= (p.Asp97=)
18g.62358320A>CCA402613358TNFRSF11Ac.500A>C (p.Asp167Ala)
n.418A>C
c.458A>C (p.Asp153Ala)
c.515A>C (p.Asp172Ala)
c.392A>C (p.Asp131Ala)
n.530A>C
c.350A>C (p.Asp117Ala)
c.290A>C (p.Asp97Ala)
18g.62358320A>GCA301696830TNFRSF11Ac.500A>G (p.Asp167Gly)
n.418A>G
c.458A>G (p.Asp153Gly)
c.515A>G (p.Asp172Gly)
c.392A>G (p.Asp131Gly)
n.530A>G
c.350A>G (p.Asp117Gly)
c.290A>G (p.Asp97Gly)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
18g.62358320A>TCA402613361TNFRSF11Ac.500A>T (p.Asp167Val)
n.418A>T
c.458A>T (p.Asp153Val)
c.515A>T (p.Asp172Val)
c.392A>T (p.Asp131Val)
n.530A>T
c.350A>T (p.Asp117Val)
c.290A>T (p.Asp97Val)
18g.62358321C>ACA402613363TNFRSF11Ac.501C>A (p.Asp167Glu)
n.419C>A
c.459C>A (p.Asp153Glu)
c.516C>A (p.Asp172Glu)
c.393C>A (p.Asp131Glu)
n.531C>A
c.351C>A (p.Asp117Glu)
c.291C>A (p.Asp97Glu)
18g.62358321C>GCA402613365TNFRSF11Ac.501C>G (p.Asp167Glu)
n.419C>G
c.459C>G (p.Asp153Glu)
c.516C>G (p.Asp172Glu)
c.393C>G (p.Asp131Glu)
n.531C>G
c.351C>G (p.Asp117Glu)
c.291C>G (p.Asp97Glu)
18g.62358321C>TCA504078156TNFRSF11Ac.501C>T (p.Asp167=)
n.419C>T
c.459C>T (p.Asp153=)
c.516C>T (p.Asp172=)
c.393C>T (p.Asp131=)
n.531C>T
c.351C>T (p.Asp117=)
c.291C>T (p.Asp97=)
18g.62358322A>CCA402613367TNFRSF11Ac.502A>C (p.Lys168Gln)
n.420A>C
c.460A>C (p.Lys154Gln)
c.517A>C (p.Lys173Gln)
c.394A>C (p.Lys132Gln)
n.532A>C
c.352A>C (p.Lys118Gln)
c.292A>C (p.Lys98Gln)
18g.62358322A>GCA402613368TNFRSF11Ac.502A>G (p.Lys168Glu)
n.420A>G
c.460A>G (p.Lys154Glu)
c.517A>G (p.Lys173Glu)
c.394A>G (p.Lys132Glu)
n.532A>G
c.352A>G (p.Lys118Glu)
c.292A>G (p.Lys98Glu)
 gnomAD v4
18g.62358322A>TCA402613370TNFRSF11Ac.502A>T (p.Lys168Ter)
n.420A>T
c.460A>T (p.Lys154Ter)
c.517A>T (p.Lys173Ter)
c.394A>T (p.Lys132Ter)
n.532A>T
c.352A>T (p.Lys118Ter)
c.292A>T (p.Lys98Ter)
18g.62358323A>CCA402613373TNFRSF11Ac.503A>C (p.Lys168Thr)
n.421A>C
c.461A>C (p.Lys154Thr)
c.518A>C (p.Lys173Thr)
c.395A>C (p.Lys132Thr)
n.533A>C
c.353A>C (p.Lys118Thr)
c.293A>C (p.Lys98Thr)
18g.62358323A>GCA402613374TNFRSF11Ac.503A>G (p.Lys168Arg)
n.421A>G
c.461A>G (p.Lys154Arg)
c.518A>G (p.Lys173Arg)
c.395A>G (p.Lys132Arg)
n.533A>G
c.353A>G (p.Lys118Arg)
c.293A>G (p.Lys98Arg)
18g.62358323A>TCA402613376TNFRSF11Ac.503A>T (p.Lys168Ile)
n.421A>T
c.461A>T (p.Lys154Ile)
c.518A>T (p.Lys173Ile)
c.395A>T (p.Lys132Ile)
n.533A>T
c.353A>T (p.Lys118Ile)
c.293A>T (p.Lys98Ile)
18g.62358324A>CCA402613379TNFRSF11Ac.504A>C (p.Lys168Asn)
n.422A>C
c.462A>C (p.Lys154Asn)
c.519A>C (p.Lys173Asn)
c.396A>C (p.Lys132Asn)
n.534A>C
c.354A>C (p.Lys118Asn)
c.294A>C (p.Lys98Asn)
18g.62358324A>GCA504078168TNFRSF11Ac.504A>G (p.Lys168=)
n.422A>G
c.462A>G (p.Lys154=)
c.519A>G (p.Lys173=)
c.396A>G (p.Lys132=)
n.534A>G
c.354A>G (p.Lys118=)
c.294A>G (p.Lys98=)
18g.62358324A>TCA402613381TNFRSF11Ac.504A>T (p.Lys168Asn)
n.422A>T
c.462A>T (p.Lys154Asn)
c.519A>T (p.Lys173Asn)
c.396A>T (p.Lys132Asn)
n.534A>T
c.354A>T (p.Lys118Asn)
c.294A>T (p.Lys98Asn)
18g.62358325T>ACA402613389TNFRSF11Ac.505T>A (p.Cys169Ser)
n.423T>A
c.463T>A (p.Cys155Ser)
c.520T>A (p.Cys174Ser)
c.397T>A (p.Cys133Ser)
n.535T>A
c.355T>A (p.Cys119Ser)
c.295T>A (p.Cys99Ser)
18g.62358325T>CCA402613384TNFRSF11Ac.505T>C (p.Cys169Arg)
n.423T>C
c.463T>C (p.Cys155Arg)
c.520T>C (p.Cys174Arg)
c.397T>C (p.Cys133Arg)
n.535T>C
c.355T>C (p.Cys119Arg)
c.295T>C (p.Cys99Arg)
18g.62358325T>GCA402613386TNFRSF11Ac.505T>G (p.Cys169Gly)
n.423T>G
c.463T>G (p.Cys155Gly)
c.520T>G (p.Cys174Gly)
c.397T>G (p.Cys133Gly)
n.535T>G
c.355T>G (p.Cys119Gly)
c.295T>G (p.Cys99Gly)
18g.62358326G>ACA402613391TNFRSF11Ac.506G>A (p.Cys169Tyr)
n.424G>A
c.464G>A (p.Cys155Tyr)
c.521G>A (p.Cys174Tyr)
c.398G>A (p.Cys133Tyr)
n.536G>A
c.356G>A (p.Cys119Tyr)
c.296G>A (p.Cys99Tyr)
18g.62358326G>CCA402613395TNFRSF11Ac.506G>C (p.Cys169Ser)
n.424G>C
c.464G>C (p.Cys155Ser)
c.521G>C (p.Cys174Ser)
c.398G>C (p.Cys133Ser)
n.536G>C
c.356G>C (p.Cys119Ser)
c.296G>C (p.Cys99Ser)
18g.62358326G>TCA402613397TNFRSF11Ac.506G>T (p.Cys169Phe)
n.424G>T
c.464G>T (p.Cys155Phe)
c.521G>T (p.Cys174Phe)
c.398G>T (p.Cys133Phe)
n.536G>T
c.356G>T (p.Cys119Phe)
c.296G>T (p.Cys99Phe)
 gnomAD v4
18g.62358327C>ACA402613400TNFRSF11Ac.507C>A (p.Cys169Ter)
n.425C>A
c.465C>A (p.Cys155Ter)
c.522C>A (p.Cys174Ter)
c.399C>A (p.Cys133Ter)
n.537C>A
c.357C>A (p.Cys119Ter)
c.297C>A (p.Cys99Ter)
18g.62358327C>GCA402613403TNFRSF11Ac.507C>G (p.Cys169Trp)
n.425C>G
c.465C>G (p.Cys155Trp)
c.522C>G (p.Cys174Trp)
c.399C>G (p.Cys133Trp)
n.537C>G
c.357C>G (p.Cys119Trp)
c.297C>G (p.Cys99Trp)
18g.62358327C>TCA504078183TNFRSF11Ac.507C>T (p.Cys169=)
n.425C>T
c.465C>T (p.Cys155=)
c.522C>T (p.Cys174=)
c.399C>T (p.Cys133=)
n.537C>T
c.357C>T (p.Cys119=)
c.297C>T (p.Cys99=)
18g.62358328A=CA2308284534TNFRSF11Ac.508A= (p.Arg170=)
n.426A=
c.466A= (p.Arg156=)
c.523A= (p.Arg175=)
c.400A= (p.Arg134=)
n.538A=
c.358A= (p.Arg120=)
c.298A= (p.Arg100=)
18g.62358328A>CCA504078186TNFRSF11Ac.508A>C (p.Arg170=)
n.426A>C
c.466A>C (p.Arg156=)
c.523A>C (p.Arg175=)
c.400A>C (p.Arg134=)
n.538A>C
c.358A>C (p.Arg120=)
c.298A>C (p.Arg100=)
18g.62358328A>GCA118112TNFRSF11Ac.508A>G (p.Arg170Gly)
n.426A>G
c.466A>G (p.Arg156Gly)
c.523A>G (p.Arg175Gly)
c.400A>G (p.Arg134Gly)
n.538A>G
c.358A>G (p.Arg120Gly)
c.298A>G (p.Arg100Gly)
 ClinVar dbSNP gnomAD v4
18g.62358328A>TCA402613406TNFRSF11Ac.508A>T (p.Arg170Ter)
n.426A>T
c.466A>T (p.Arg156Ter)
c.523A>T (p.Arg175Ter)
c.400A>T (p.Arg134Ter)
n.538A>T
c.358A>T (p.Arg120Ter)
c.298A>T (p.Arg100Ter)
18g.62358329G>ACA402613409TNFRSF11Ac.509G>A (p.Arg170Lys)
n.427G>A
c.467G>A (p.Arg156Lys)
c.524G>A (p.Arg175Lys)
c.401G>A (p.Arg134Lys)
n.539G>A
c.359G>A (p.Arg120Lys)
c.299G>A (p.Arg100Lys)
18g.62358329G>CCA402613410TNFRSF11Ac.509G>C (p.Arg170Thr)
n.427G>C
c.467G>C (p.Arg156Thr)
c.524G>C (p.Arg175Thr)
c.401G>C (p.Arg134Thr)
n.539G>C
c.359G>C (p.Arg120Thr)
c.299G>C (p.Arg100Thr)
18g.62358329G>TCA402613413TNFRSF11Ac.509G>T (p.Arg170Ile)
n.427G>T
c.467G>T (p.Arg156Ile)
c.524G>T (p.Arg175Ile)
c.401G>T (p.Arg134Ile)
n.539G>T
c.359G>T (p.Arg120Ile)
c.299G>T (p.Arg100Ile)
 gnomAD v4
18g.62358330A>CCA402613417TNFRSF11Ac.510A>C (p.Arg170Ser)
n.428A>C
c.468A>C (p.Arg156Ser)
c.525A>C (p.Arg175Ser)
c.402A>C (p.Arg134Ser)
n.540A>C
c.360A>C (p.Arg120Ser)
c.300A>C (p.Arg100Ser)
18g.62358330A>GCA504078196TNFRSF11Ac.510A>G (p.Arg170=)
n.428A>G
c.468A>G (p.Arg156=)
c.525A>G (p.Arg175=)
c.402A>G (p.Arg134=)
n.540A>G
c.360A>G (p.Arg120=)
c.300A>G (p.Arg100=)
18g.62358330A>TCA402613420TNFRSF11Ac.510A>T (p.Arg170Ser)
n.428A>T
c.468A>T (p.Arg156Ser)
c.525A>T (p.Arg175Ser)
c.402A>T (p.Arg134Ser)
n.540A>T
c.360A>T (p.Arg120Ser)
c.300A>T (p.Arg100Ser)
18g.62358331C>ACA402613426TNFRSF11Ac.511C>A (p.Pro171Thr)
n.429C>A
c.469C>A (p.Pro157Thr)
c.526C>A (p.Pro176Thr)
c.403C>A (p.Pro135Thr)
n.541C>A
c.361C>A (p.Pro121Thr)
c.301C>A (p.Pro101Thr)
18g.62358331C>GCA402613427TNFRSF11Ac.511C>G (p.Pro171Ala)
n.429C>G
c.469C>G (p.Pro157Ala)
c.526C>G (p.Pro176Ala)
c.403C>G (p.Pro135Ala)
n.541C>G
c.361C>G (p.Pro121Ala)
c.301C>G (p.Pro101Ala)
18g.62358331C>TCA402613422TNFRSF11Ac.511C>T (p.Pro171Ser)
n.429C>T
c.469C>T (p.Pro157Ser)
c.526C>T (p.Pro176Ser)
c.403C>T (p.Pro135Ser)
n.541C>T
c.361C>T (p.Pro121Ser)
c.301C>T (p.Pro101Ser)

Number of alleles fetched