Chr Mutation (hg38) CAid Gene Transcript Linkouts
13g.42606466C>TCA2622837726TNFSF11c.533-31C>T (n.533-31C>T)
c.392-31C>T (n.392-31C>T)
c.314-31C>T (n.314-31C>T)
c.371-31C>T (n.371-31C>T)
 gnomAD v4
13g.42606467T>GCA2544857782TNFSF11c.533-30T>G (n.533-30T>G)
c.392-30T>G (n.392-30T>G)
c.314-30T>G (n.314-30T>G)
c.371-30T>G (n.371-30T>G)
13g.42606471_42606475dupCA2622837727TNFSF11c.533-26_533-22dup (n.533-26_533-22dup)
c.392-26_392-22dup (n.392-26_392-22dup)
c.314-26_314-22dup (n.314-26_314-22dup)
c.371-26_371-22dup (n.371-26_371-22dup)
 gnomAD v4
13g.42606473A>CCA2622837728TNFSF11c.533-24A>C (n.533-24A>C)
c.392-24A>C (n.392-24A>C)
c.314-24A>C (n.314-24A>C)
c.371-24A>C (n.371-24A>C)
 gnomAD v4
13g.42606473A>GCA2622837729TNFSF11c.533-24A>G (n.533-24A>G)
c.392-24A>G (n.392-24A>G)
c.314-24A>G (n.314-24A>G)
c.371-24A>G (n.371-24A>G)
 gnomAD v4
13g.42606475C=CA2087395029TNFSF11c.533-22C= (n.533-22C=)
c.392-22C= (n.392-22C=)
c.314-22C= (n.314-22C=)
c.371-22C= (n.371-22C=)
13g.42606475C>TCA249053390TNFSF11c.533-22C>T (n.533-22C>T)
c.392-22C>T (n.392-22C>T)
c.314-22C>T (n.314-22C>T)
c.371-22C>T (n.371-22C>T)
 dbSNP gnomAD v4
13g.42606476T>ACA2727969257TNFSF11c.533-21T>A (n.533-21T>A)
c.392-21T>A (n.392-21T>A)
c.314-21T>A (n.314-21T>A)
c.371-21T>A (n.371-21T>A)
 dbSNP
13g.42606477T>CCA2575404248TNFSF11c.533-20T>C (n.533-20T>C)
c.392-20T>C (n.392-20T>C)
c.314-20T>C (n.314-20T>C)
c.371-20T>C (n.371-20T>C)
13g.42606479T>ACA2622837730TNFSF11c.533-18T>A (n.533-18T>A)
c.392-18T>A (n.392-18T>A)
c.314-18T>A (n.314-18T>A)
c.371-18T>A (n.371-18T>A)
 gnomAD v4
13g.42606479T>CCA2739277590TNFSF11c.533-18T>C (n.533-18T>C)
c.392-18T>C (n.392-18T>C)
c.314-18T>C (n.314-18T>C)
c.371-18T>C (n.371-18T>C)
 ClinVar
13g.42606480G>CCA698179489TNFSF11c.533-17G>C (n.533-17G>C)
c.392-17G>C (n.392-17G>C)
c.314-17G>C (n.314-17G>C)
c.371-17G>C (n.371-17G>C)
 dbSNP gnomAD v3 gnomAD v4
13g.42606480G=CA2087395030TNFSF11c.533-17G= (n.533-17G=)
c.392-17G= (n.392-17G=)
c.314-17G= (n.314-17G=)
c.371-17G= (n.371-17G=)
13g.42606481C=CA2087395031TNFSF11c.533-16C= (n.533-16C=)
c.392-16C= (n.392-16C=)
c.314-16C= (n.314-16C=)
c.371-16C= (n.371-16C=)
13g.42606481C>TCA249053391TNFSF11c.533-16C>T (n.533-16C>T)
c.392-16C>T (n.392-16C>T)
c.314-16C>T (n.314-16C>T)
c.371-16C>T (n.371-16C>T)
 dbSNP gnomAD v4
13g.42606482C=CA2087395032TNFSF11c.533-15C= (n.533-15C=)
c.392-15C= (n.392-15C=)
c.314-15C= (n.314-15C=)
c.371-15C= (n.371-15C=)
13g.42606482C>TCA6967266TNFSF11c.533-15C>T (n.533-15C>T)
c.392-15C>T (n.392-15C>T)
c.314-15C>T (n.314-15C>T)
c.371-15C>T (n.371-15C>T)
 dbSNP ExAC gnomAD v2 gnomAD v4
13g.42606483T>CCA698179495TNFSF11c.533-14T>C (n.533-14T>C)
c.392-14T>C (n.392-14T>C)
c.314-14T>C (n.314-14T>C)
c.371-14T>C (n.371-14T>C)
 dbSNP gnomAD v4
13g.42606483T=CA2087395033TNFSF11c.533-14T= (n.533-14T=)
c.392-14T= (n.392-14T=)
c.314-14T= (n.314-14T=)
c.371-14T= (n.371-14T=)
13g.42606484C>GCA2622837731TNFSF11c.533-13C>G (n.533-13C>G)
c.392-13C>G (n.392-13C>G)
c.314-13C>G (n.314-13C>G)
c.371-13C>G (n.371-13C>G)
 dbSNP gnomAD v4
13g.42606485T>ACA698179497TNFSF11c.533-12T>A (n.533-12T>A)
c.392-12T>A (n.392-12T>A)
c.314-12T>A (n.314-12T>A)
c.371-12T>A (n.371-12T>A)
 dbSNP gnomAD v3 gnomAD v4
13g.42606485T>CCA2622837732TNFSF11c.533-12T>C (n.533-12T>C)
c.392-12T>C (n.392-12T>C)
c.314-12T>C (n.314-12T>C)
c.371-12T>C (n.371-12T>C)
 gnomAD v4
13g.42606485T=CA2087395034TNFSF11c.533-12T= (n.533-12T=)
c.392-12T= (n.392-12T=)
c.314-12T= (n.314-12T=)
c.371-12T= (n.371-12T=)
13g.42606486C>GCA2622837733TNFSF11c.533-11C>G (n.533-11C>G)
c.392-11C>G (n.392-11C>G)
c.314-11C>G (n.314-11C>G)
c.371-11C>G (n.371-11C>G)
 gnomAD v4
13g.42606488_42606491delinsTCTCCA2087395035TNFSF11c.533-9_533-6delinsTCTC (n.533-9_533-6delinsTCTC)
c.392-9_392-6delinsTCTC (n.392-9_392-6delinsTCTC)
c.314-9_314-6delinsTCTC (n.314-9_314-6delinsTCTC)
c.371-9_371-6delinsTCTC (n.371-9_371-6delinsTCTC)
13g.42606489C>ACA2580087527TNFSF11c.533-8C>A (n.533-8C>A)
c.392-8C>A (n.392-8C>A)
c.314-8C>A (n.314-8C>A)
c.371-8C>A (n.371-8C>A)
 ClinVar
13g.42606489C=CA2087395036TNFSF11c.533-8C= (n.533-8C=)
c.392-8C= (n.392-8C=)
c.314-8C= (n.314-8C=)
c.371-8C= (n.371-8C=)
13g.42606489C>TCA955380252TNFSF11c.533-8C>T (n.533-8C>T)
c.392-8C>T (n.392-8C>T)
c.314-8C>T (n.314-8C>T)
c.371-8C>T (n.371-8C>T)
 ClinVar dbSNP gnomAD v3 gnomAD v4
13g.42606490_42606492delCA609930840TNFSF11c.533-7_533-5del (n.533-7_533-5del)
c.392-7_392-5del (n.392-7_392-5del)
c.314-7_314-5del (n.314-7_314-5del)
c.371-7_371-5del (n.371-7_371-5del)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
13g.42606491C=CA2087395037TNFSF11c.533-6C= (n.533-6C=)
c.392-6C= (n.392-6C=)
c.314-6C= (n.314-6C=)
c.371-6C= (n.371-6C=)
13g.42606491C>GCA609930841TNFSF11c.533-6C>G (n.533-6C>G)
c.392-6C>G (n.392-6C>G)
c.314-6C>G (n.314-6C>G)
c.371-6C>G (n.371-6C>G)
 dbSNP gnomAD v2
13g.42606492C=CA2087395038TNFSF11c.533-5C= (n.533-5C=)
c.392-5C= (n.392-5C=)
c.314-5C= (n.314-5C=)
c.371-5C= (n.371-5C=)
13g.42606492C>TCA2087395039TNFSF11c.533-5C>T (n.533-5C>T)
c.392-5C>T (n.392-5C>T)
c.314-5C>T (n.314-5C>T)
c.371-5C>T (n.371-5C>T)
 dbSNP gnomAD v4
13g.42606494C=CA2087395040TNFSF11c.533-3C= (n.533-3C=)
c.392-3C= (n.392-3C=)
c.314-3C= (n.314-3C=)
c.371-3C= (n.371-3C=)
13g.42606494C>TCA955380255TNFSF11c.533-3C>T (n.533-3C>T)
c.392-3C>T (n.392-3C>T)
c.314-3C>T (n.314-3C>T)
c.371-3C>T (n.371-3C>T)
 dbSNP gnomAD v3 gnomAD v4
13g.42606495A>CCA388220737TNFSF11c.533-2A>C (n.533-2A>C)
c.392-2A>C (n.392-2A>C)
c.314-2A>C (n.314-2A>C)
c.371-2A>C (n.371-2A>C)
13g.42606495A>GCA388220735TNFSF11c.533-2A>G (n.533-2A>G)
c.392-2A>G (n.392-2A>G)
c.314-2A>G (n.314-2A>G)
c.371-2A>G (n.371-2A>G)
13g.42606495A>TCA388220736TNFSF11c.533-2A>T (n.533-2A>T)
c.392-2A>T (n.392-2A>T)
c.314-2A>T (n.314-2A>T)
c.371-2A>T (n.371-2A>T)
13g.42606496G>ACA388220738TNFSF11c.533-1G>A (n.533-1G>A)
c.392-1G>A (n.392-1G>A)
c.314-1G>A (n.314-1G>A)
c.371-1G>A (n.371-1G>A)
13g.42606496G>CCA388220739TNFSF11c.533-1G>C (n.533-1G>C)
c.392-1G>C (n.392-1G>C)
c.314-1G>C (n.314-1G>C)
c.371-1G>C (n.371-1G>C)
 dbSNP gnomAD v2
13g.42606496G=CA2087395041TNFSF11c.533-1G= (n.533-1G=)
c.392-1G= (n.392-1G=)
c.314-1G= (n.314-1G=)
c.371-1G= (n.371-1G=)
13g.42606496G>TCA388220740TNFSF11c.533-1G>T (n.533-1G>T)
c.392-1G>T (n.392-1G>T)
c.314-1G>T (n.314-1G>T)
c.371-1G>T (n.371-1G>T)
 gnomAD v4
13g.42606497G>ACA388220741TNFSF11c.533G>A (p.Gly178Asp)
c.392G>A (p.Gly131Asp)
c.314G>A (p.Gly105Asp)
c.371G>A (p.Gly124Asp)
 gnomAD v4
13g.42606497G>CCA388220742TNFSF11c.533G>C (p.Gly178Ala)
c.392G>C (p.Gly131Ala)
c.314G>C (p.Gly105Ala)
c.371G>C (p.Gly124Ala)
13g.42606497G=CA2087395042TNFSF11c.533G= (p.Gly178=)
c.392G= (p.Gly131=)
c.314G= (p.Gly105=)
c.371G= (p.Gly124=)
13g.42606497G>TCA249053392TNFSF11c.533G>T (p.Gly178Val)
c.392G>T (p.Gly131Val)
c.314G>T (p.Gly105Val)
c.371G>T (p.Gly124Val)
 ClinVar dbSNP gnomAD v2 gnomAD v4
13g.42606498T>ACA483604978TNFSF11c.534T>A (p.Gly178=)
c.393T>A (p.Gly131=)
c.315T>A (p.Gly105=)
c.372T>A (p.Gly124=)
13g.42606498T>CCA6967267TNFSF11c.534T>C (p.Gly178=)
c.393T>C (p.Gly131=)
c.315T>C (p.Gly105=)
c.372T>C (p.Gly124=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
13g.42606498T>GCA483604977TNFSF11c.534T>G (p.Gly178=)
c.393T>G (p.Gly131=)
c.315T>G (p.Gly105=)
c.372T>G (p.Gly124=)
13g.42606498T=CA2087395043TNFSF11c.534T= (p.Gly178=)
c.393T= (p.Gly131=)
c.315T= (p.Gly105=)
c.372T= (p.Gly124=)
13g.42606499T>ACA388220743TNFSF11c.535T>A (p.Ser179Thr)
c.394T>A (p.Ser132Thr)
c.316T>A (p.Ser106Thr)
c.373T>A (p.Ser125Thr)
13g.42606499T>CCA388220744TNFSF11c.535T>C (p.Ser179Pro)
c.394T>C (p.Ser132Pro)
c.316T>C (p.Ser106Pro)
c.373T>C (p.Ser125Pro)
13g.42606499T>GCA388220745TNFSF11c.535T>G (p.Ser179Ala)
c.394T>G (p.Ser132Ala)
c.316T>G (p.Ser106Ala)
c.373T>G (p.Ser125Ala)
13g.42606500C>ACA388220746TNFSF11c.536C>A (p.Ser179Tyr)
c.395C>A (p.Ser132Tyr)
c.317C>A (p.Ser106Tyr)
c.374C>A (p.Ser125Tyr)
13g.42606500C>GCA388220747TNFSF11c.536C>G (p.Ser179Cys)
c.395C>G (p.Ser132Cys)
c.317C>G (p.Ser106Cys)
c.374C>G (p.Ser125Cys)
13g.42606500C>TCA388220748TNFSF11c.536C>T (p.Ser179Phe)
c.395C>T (p.Ser132Phe)
c.317C>T (p.Ser106Phe)
c.374C>T (p.Ser125Phe)
 gnomAD v4 COSMIC
13g.42606501C>ACA483604979TNFSF11c.537C>A (p.Ser179=)
c.396C>A (p.Ser132=)
c.318C>A (p.Ser106=)
c.375C>A (p.Ser125=)
13g.42606501C>GCA483604981TNFSF11c.537C>G (p.Ser179=)
c.396C>G (p.Ser132=)
c.318C>G (p.Ser106=)
c.375C>G (p.Ser125=)
13g.42606501C>TCA483604980TNFSF11c.537C>T (p.Ser179=)
c.396C>T (p.Ser132=)
c.318C>T (p.Ser106=)
c.375C>T (p.Ser125=)
13g.42606502C>ACA388220749TNFSF11c.538C>A (p.His180Asn)
c.397C>A (p.His133Asn)
c.319C>A (p.His107Asn)
c.376C>A (p.His126Asn)
13g.42606502C>GCA388220751TNFSF11c.538C>G (p.His180Asp)
c.397C>G (p.His133Asp)
c.319C>G (p.His107Asp)
c.376C>G (p.His126Asp)
13g.42606502C>TCA388220750TNFSF11c.538C>T (p.His180Tyr)
c.397C>T (p.His133Tyr)
c.319C>T (p.His107Tyr)
c.376C>T (p.His126Tyr)
13g.42606503A=CA2087395044TNFSF11c.539A= (p.His180=)
c.398A= (p.His133=)
c.320A= (p.His107=)
c.377A= (p.His126=)
13g.42606503A>CCA388220752TNFSF11c.539A>C (p.His180Pro)
c.398A>C (p.His133Pro)
c.320A>C (p.His107Pro)
c.377A>C (p.His126Pro)
13g.42606503A>GCA6967268TNFSF11c.539A>G (p.His180Arg)
c.398A>G (p.His133Arg)
c.320A>G (p.His107Arg)
c.377A>G (p.His126Arg)
 dbSNP ExAC gnomAD v2 gnomAD v4
13g.42606503A>TCA388220753TNFSF11c.539A>T (p.His180Leu)
c.398A>T (p.His133Leu)
c.320A>T (p.His107Leu)
c.377A>T (p.His126Leu)
13g.42606504T>ACA388220754TNFSF11c.540T>A (p.His180Gln)
c.399T>A (p.His133Gln)
c.321T>A (p.His107Gln)
c.378T>A (p.His126Gln)
13g.42606504T>CCA483604982TNFSF11c.540T>C (p.His180=)
c.399T>C (p.His133=)
c.321T>C (p.His107=)
c.378T>C (p.His126=)
13g.42606504T>GCA388220755TNFSF11c.540T>G (p.His180Gln)
c.399T>G (p.His133Gln)
c.321T>G (p.His107Gln)
c.378T>G (p.His126Gln)
 ClinVar
13g.42606505A>CCA388220756TNFSF11c.541A>C (p.Lys181Gln)
c.400A>C (p.Lys134Gln)
c.322A>C (p.Lys108Gln)
c.379A>C (p.Lys127Gln)
13g.42606505A>GCA388220757TNFSF11c.541A>G (p.Lys181Glu)
c.400A>G (p.Lys134Glu)
c.322A>G (p.Lys108Glu)
c.379A>G (p.Lys127Glu)
13g.42606505A>TCA388220758TNFSF11c.541A>T (p.Lys181Ter)
c.400A>T (p.Lys134Ter)
c.322A>T (p.Lys108Ter)
c.379A>T (p.Lys127Ter)
13g.42606506A>CCA388220759TNFSF11c.542A>C (p.Lys181Thr)
c.401A>C (p.Lys134Thr)
c.323A>C (p.Lys108Thr)
c.380A>C (p.Lys127Thr)
13g.42606506A>GCA388220760TNFSF11c.542A>G (p.Lys181Arg)
c.401A>G (p.Lys134Arg)
c.323A>G (p.Lys108Arg)
c.380A>G (p.Lys127Arg)
13g.42606506A>TCA388220761TNFSF11c.542A>T (p.Lys181Ile)
c.401A>T (p.Lys134Ile)
c.323A>T (p.Lys108Ile)
c.380A>T (p.Lys127Ile)
13g.42606507A>CCA388220762TNFSF11c.543A>C (p.Lys181Asn)
c.402A>C (p.Lys134Asn)
c.324A>C (p.Lys108Asn)
c.381A>C (p.Lys127Asn)
13g.42606507A>GCA483604983TNFSF11c.543A>G (p.Lys181=)
c.402A>G (p.Lys134=)
c.324A>G (p.Lys108=)
c.381A>G (p.Lys127=)
 gnomAD v4
13g.42606507A>TCA388220763TNFSF11c.543A>T (p.Lys181Asn)
c.402A>T (p.Lys134Asn)
c.324A>T (p.Lys108Asn)
c.381A>T (p.Lys127Asn)
13g.42606508G>ACA6967269TNFSF11c.544G>A (p.Val182Met)
c.403G>A (p.Val135Met)
c.325G>A (p.Val109Met)
c.382G>A (p.Val128Met)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
13g.42606508G>CCA388220765TNFSF11c.544G>C (p.Val182Leu)
c.403G>C (p.Val135Leu)
c.325G>C (p.Val109Leu)
c.382G>C (p.Val128Leu)
13g.42606508G=CA2087395045TNFSF11c.544G= (p.Val182=)
c.403G= (p.Val135=)
c.325G= (p.Val109=)
c.382G= (p.Val128=)
13g.42606508G>TCA388220764TNFSF11c.544G>T (p.Val182Leu)
c.403G>T (p.Val135Leu)
c.325G>T (p.Val109Leu)
c.382G>T (p.Val128Leu)
13g.42606509T>ACA388220766TNFSF11c.545T>A (p.Val182Glu)
c.404T>A (p.Val135Glu)
c.326T>A (p.Val109Glu)
c.383T>A (p.Val128Glu)
13g.42606509T>CCA388220767TNFSF11c.545T>C (p.Val182Ala)
c.404T>C (p.Val135Ala)
c.326T>C (p.Val109Ala)
c.383T>C (p.Val128Ala)
13g.42606509T>GCA388220768TNFSF11c.545T>G (p.Val182Gly)
c.404T>G (p.Val135Gly)
c.326T>G (p.Val109Gly)
c.383T>G (p.Val128Gly)
13g.42606510G>ACA483604984TNFSF11c.546G>A (p.Val182=)
c.405G>A (p.Val135=)
c.327G>A (p.Val109=)
c.384G>A (p.Val128=)
13g.42606510G>CCA483604985TNFSF11c.546G>C (p.Val182=)
c.405G>C (p.Val135=)
c.327G>C (p.Val109=)
c.384G>C (p.Val128=)
13g.42606510G>TCA483604986TNFSF11c.546G>T (p.Val182=)
c.405G>T (p.Val135=)
c.327G>T (p.Val109=)
c.384G>T (p.Val128=)
13g.42606511A>CCA388220769TNFSF11c.547A>C (p.Ser183Arg)
c.406A>C (p.Ser136Arg)
c.328A>C (p.Ser110Arg)
c.385A>C (p.Ser129Arg)
13g.42606511A>GCA388220770TNFSF11c.547A>G (p.Ser183Gly)
c.406A>G (p.Ser136Gly)
c.328A>G (p.Ser110Gly)
c.385A>G (p.Ser129Gly)
13g.42606511A>TCA388220771TNFSF11c.547A>T (p.Ser183Cys)
c.406A>T (p.Ser136Cys)
c.328A>T (p.Ser110Cys)
c.385A>T (p.Ser129Cys)
13g.42606512G>ACA388220772TNFSF11c.548G>A (p.Ser183Asn)
c.407G>A (p.Ser136Asn)
c.329G>A (p.Ser110Asn)
c.386G>A (p.Ser129Asn)
 gnomAD v4
13g.42606512G>CCA388220773TNFSF11c.548G>C (p.Ser183Thr)
c.407G>C (p.Ser136Thr)
c.329G>C (p.Ser110Thr)
c.386G>C (p.Ser129Thr)
13g.42606512G>TCA388220774TNFSF11c.548G>T (p.Ser183Ile)
c.407G>T (p.Ser136Ile)
c.329G>T (p.Ser110Ile)
c.386G>T (p.Ser129Ile)
 COSMIC
13g.42606513T>ACA388220776TNFSF11c.549T>A (p.Ser183Arg)
c.408T>A (p.Ser136Arg)
c.330T>A (p.Ser110Arg)
c.387T>A (p.Ser129Arg)
13g.42606513T>CCA483604987TNFSF11c.549T>C (p.Ser183=)
c.408T>C (p.Ser136=)
c.330T>C (p.Ser110=)
c.387T>C (p.Ser129=)
 dbSNP gnomAD v2 gnomAD v4
13g.42606513T>GCA388220778TNFSF11c.549T>G (p.Ser183Arg)
c.408T>G (p.Ser136Arg)
c.330T>G (p.Ser110Arg)
c.387T>G (p.Ser129Arg)
 dbSNP
13g.42606513T=CA2087395046TNFSF11c.549T= (p.Ser183=)
c.408T= (p.Ser136=)
c.330T= (p.Ser110=)
c.387T= (p.Ser129=)
13g.42606514C>ACA249053393TNFSF11c.550C>A (p.Leu184Met)
c.409C>A (p.Leu137Met)
c.331C>A (p.Leu111Met)
c.388C>A (p.Leu130Met)
 dbSNP gnomAD v4
13g.42606514C=CA2087395047TNFSF11c.550C= (p.Leu184=)
c.409C= (p.Leu137=)
c.331C= (p.Leu111=)
c.388C= (p.Leu130=)
13g.42606514C>GCA388220780TNFSF11c.550C>G (p.Leu184Val)
c.409C>G (p.Leu137Val)
c.331C>G (p.Leu111Val)
c.388C>G (p.Leu130Val)
13g.42606514C>TCA483604988TNFSF11c.550C>T (p.Leu184=)
c.409C>T (p.Leu137=)
c.331C>T (p.Leu111=)
c.388C>T (p.Leu130=)
13g.42606515T>ACA388220783TNFSF11c.551T>A (p.Leu184Gln)
c.410T>A (p.Leu137Gln)
c.332T>A (p.Leu111Gln)
c.389T>A (p.Leu130Gln)
13g.42606515T>CCA388220787TNFSF11c.551T>C (p.Leu184Pro)
c.410T>C (p.Leu137Pro)
c.332T>C (p.Leu111Pro)
c.389T>C (p.Leu130Pro)
13g.42606515T>GCA388220785TNFSF11c.551T>G (p.Leu184Arg)
c.410T>G (p.Leu137Arg)
c.332T>G (p.Leu111Arg)
c.389T>G (p.Leu130Arg)
13g.42606516G>ACA483604989TNFSF11c.552G>A (p.Leu184=)
c.411G>A (p.Leu137=)
c.333G>A (p.Leu111=)
c.390G>A (p.Leu130=)
 ClinVar gnomAD v4
13g.42606516G>CCA483604990TNFSF11c.552G>C (p.Leu184=)
c.411G>C (p.Leu137=)
c.333G>C (p.Leu111=)
c.390G>C (p.Leu130=)
13g.42606516G>TCA483604991TNFSF11c.552G>T (p.Leu184=)
c.411G>T (p.Leu137=)
c.333G>T (p.Leu111=)
c.390G>T (p.Leu130=)
13g.42606517T>ACA388220789TNFSF11c.553T>A (p.Ser185Thr)
c.412T>A (p.Ser138Thr)
c.334T>A (p.Ser112Thr)
c.391T>A (p.Ser131Thr)
13g.42606517T>CCA388220793TNFSF11c.553T>C (p.Ser185Pro)
c.412T>C (p.Ser138Pro)
c.334T>C (p.Ser112Pro)
c.391T>C (p.Ser131Pro)
13g.42606517T>GCA388220791TNFSF11c.553T>G (p.Ser185Ala)
c.412T>G (p.Ser138Ala)
c.334T>G (p.Ser112Ala)
c.391T>G (p.Ser131Ala)
13g.42606518C>ACA388220795TNFSF11c.554C>A (p.Ser185Tyr)
c.413C>A (p.Ser138Tyr)
c.335C>A (p.Ser112Tyr)
c.392C>A (p.Ser131Tyr)
13g.42606518C>GCA388220797TNFSF11c.554C>G (p.Ser185Cys)
c.413C>G (p.Ser138Cys)
c.335C>G (p.Ser112Cys)
c.392C>G (p.Ser131Cys)
13g.42606518C>TCA388220799TNFSF11c.554C>T (p.Ser185Phe)
c.413C>T (p.Ser138Phe)
c.335C>T (p.Ser112Phe)
c.392C>T (p.Ser131Phe)
13g.42606519C>ACA483604992TNFSF11c.555C>A (p.Ser185=)
c.414C>A (p.Ser138=)
c.336C>A (p.Ser112=)
c.393C>A (p.Ser131=)
13g.42606519C>GCA483604993TNFSF11c.555C>G (p.Ser185=)
c.414C>G (p.Ser138=)
c.336C>G (p.Ser112=)
c.393C>G (p.Ser131=)
13g.42606519C>TCA483604994TNFSF11c.555C>T (p.Ser185=)
c.414C>T (p.Ser138=)
c.336C>T (p.Ser112=)
c.393C>T (p.Ser131=)
13g.42606520T>ACA388220801TNFSF11c.556T>A (p.Ser186Thr)
c.415T>A (p.Ser139Thr)
c.337T>A (p.Ser113Thr)
c.394T>A (p.Ser132Thr)
13g.42606520T>CCA388220803TNFSF11c.556T>C (p.Ser186Pro)
c.415T>C (p.Ser139Pro)
c.337T>C (p.Ser113Pro)
c.394T>C (p.Ser132Pro)
13g.42606520T>GCA388220805TNFSF11c.556T>G (p.Ser186Ala)
c.415T>G (p.Ser139Ala)
c.337T>G (p.Ser113Ala)
c.394T>G (p.Ser132Ala)
13g.42606521C>ACA388220811TNFSF11c.557C>A (p.Ser186Tyr)
c.416C>A (p.Ser139Tyr)
c.338C>A (p.Ser113Tyr)
c.395C>A (p.Ser132Tyr)
13g.42606521C>GCA388220809TNFSF11c.557C>G (p.Ser186Cys)
c.416C>G (p.Ser139Cys)
c.338C>G (p.Ser113Cys)
c.395C>G (p.Ser132Cys)
13g.42606521C>TCA388220808TNFSF11c.557C>T (p.Ser186Phe)
c.416C>T (p.Ser139Phe)
c.338C>T (p.Ser113Phe)
c.395C>T (p.Ser132Phe)
13g.42606522T>ACA483604995TNFSF11c.558T>A (p.Ser186=)
c.417T>A (p.Ser139=)
c.339T>A (p.Ser113=)
c.396T>A (p.Ser132=)
13g.42606522T>CCA483604996TNFSF11c.558T>C (p.Ser186=)
c.417T>C (p.Ser139=)
c.339T>C (p.Ser113=)
c.396T>C (p.Ser132=)
13g.42606522T>GCA483604997TNFSF11c.558T>G (p.Ser186=)
c.417T>G (p.Ser139=)
c.339T>G (p.Ser113=)
c.396T>G (p.Ser132=)
13g.42606523T>ACA388220814TNFSF11c.559T>A (p.Trp187Arg)
c.418T>A (p.Trp140Arg)
c.340T>A (p.Trp114Arg)
c.397T>A (p.Trp133Arg)
13g.42606523T>CCA388220815TNFSF11c.559T>C (p.Trp187Arg)
c.418T>C (p.Trp140Arg)
c.340T>C (p.Trp114Arg)
c.397T>C (p.Trp133Arg)
13g.42606523T>GCA388220816TNFSF11c.559T>G (p.Trp187Gly)
c.418T>G (p.Trp140Gly)
c.340T>G (p.Trp114Gly)
c.397T>G (p.Trp133Gly)
13g.42606524G>ACA388220818TNFSF11c.560G>A (p.Trp187Ter)
c.419G>A (p.Trp140Ter)
c.341G>A (p.Trp114Ter)
c.398G>A (p.Trp133Ter)
13g.42606524G>CCA388220820TNFSF11c.560G>C (p.Trp187Ser)
c.419G>C (p.Trp140Ser)
c.341G>C (p.Trp114Ser)
c.398G>C (p.Trp133Ser)
13g.42606524G>TCA388220822TNFSF11c.560G>T (p.Trp187Leu)
c.419G>T (p.Trp140Leu)
c.341G>T (p.Trp114Leu)
c.398G>T (p.Trp133Leu)
13g.42606525G>ACA388220824TNFSF11c.561G>A (p.Trp187Ter)
c.420G>A (p.Trp140Ter)
c.342G>A (p.Trp114Ter)
c.399G>A (p.Trp133Ter)
13g.42606525G>CCA388220828TNFSF11c.561G>C (p.Trp187Cys)
c.420G>C (p.Trp140Cys)
c.342G>C (p.Trp114Cys)
c.399G>C (p.Trp133Cys)
13g.42606525G>TCA388220827TNFSF11c.561G>T (p.Trp187Cys)
c.420G>T (p.Trp140Cys)
c.342G>T (p.Trp114Cys)
c.399G>T (p.Trp133Cys)
13g.42606526T>ACA388220831TNFSF11c.562T>A (p.Tyr188Asn)
c.421T>A (p.Tyr141Asn)
c.343T>A (p.Tyr115Asn)
c.400T>A (p.Tyr134Asn)
13g.42606526T>CCA388220833TNFSF11c.562T>C (p.Tyr188His)
c.421T>C (p.Tyr141His)
c.343T>C (p.Tyr115His)
c.400T>C (p.Tyr134His)
13g.42606526T>GCA388220835TNFSF11c.562T>G (p.Tyr188Asp)
c.421T>G (p.Tyr141Asp)
c.343T>G (p.Tyr115Asp)
c.400T>G (p.Tyr134Asp)
13g.42606527A=CA2087395048TNFSF11c.563A= (p.Tyr188=)
c.422A= (p.Tyr141=)
c.344A= (p.Tyr115=)
c.401A= (p.Tyr134=)
13g.42606527A>CCA388220837TNFSF11c.563A>C (p.Tyr188Ser)
c.422A>C (p.Tyr141Ser)
c.344A>C (p.Tyr115Ser)
c.401A>C (p.Tyr134Ser)
13g.42606527A>GCA6967270TNFSF11c.563A>G (p.Tyr188Cys)
c.422A>G (p.Tyr141Cys)
c.344A>G (p.Tyr115Cys)
c.401A>G (p.Tyr134Cys)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
13g.42606527A>TCA388220839TNFSF11c.563A>T (p.Tyr188Phe)
c.422A>T (p.Tyr141Phe)
c.344A>T (p.Tyr115Phe)
c.401A>T (p.Tyr134Phe)
13g.42606528C>ACA388220841TNFSF11c.564C>A (p.Tyr188Ter)
c.423C>A (p.Tyr141Ter)
c.345C>A (p.Tyr115Ter)
c.402C>A (p.Tyr134Ter)
13g.42606528C=CA2087395049TNFSF11c.564C= (p.Tyr188=)
c.423C= (p.Tyr141=)
c.345C= (p.Tyr115=)
c.402C= (p.Tyr134=)
13g.42606528C>GCA388220843TNFSF11c.564C>G (p.Tyr188Ter)
c.423C>G (p.Tyr141Ter)
c.345C>G (p.Tyr115Ter)
c.402C>G (p.Tyr134Ter)
13g.42606528C>TCA483604998TNFSF11c.564C>T (p.Tyr188=)
c.423C>T (p.Tyr141=)
c.345C>T (p.Tyr115=)
c.402C>T (p.Tyr134=)
 dbSNP gnomAD v2 gnomAD v4
13g.42606529C>ACA388220845TNFSF11c.565C>A (p.His189Asn)
c.424C>A (p.His142Asn)
c.346C>A (p.His116Asn)
c.403C>A (p.His135Asn)
13g.42606529C=CA2087395050TNFSF11c.565C= (p.His189=)
c.424C= (p.His142=)
c.346C= (p.His116=)
c.403C= (p.His135=)
13g.42606529C>GCA388220848TNFSF11c.565C>G (p.His189Asp)
c.424C>G (p.His142Asp)
c.346C>G (p.His116Asp)
c.403C>G (p.His135Asp)
13g.42606529C>TCA388220850TNFSF11c.565C>T (p.His189Tyr)
c.424C>T (p.His142Tyr)
c.346C>T (p.His116Tyr)
c.403C>T (p.His135Tyr)
 dbSNP gnomAD v3 gnomAD v4
13g.42606530A>CCA388220851TNFSF11c.566A>C (p.His189Pro)
c.425A>C (p.His142Pro)
c.347A>C (p.His116Pro)
c.404A>C (p.His135Pro)
13g.42606530A>GCA388220856TNFSF11c.566A>G (p.His189Arg)
c.425A>G (p.His142Arg)
c.347A>G (p.His116Arg)
c.404A>G (p.His135Arg)
13g.42606530A>TCA388220853TNFSF11c.566A>T (p.His189Leu)
c.425A>T (p.His142Leu)
c.347A>T (p.His116Leu)
c.404A>T (p.His135Leu)
13g.42606531T>ACA388220858TNFSF11c.567T>A (p.His189Gln)
c.426T>A (p.His142Gln)
c.348T>A (p.His116Gln)
c.405T>A (p.His135Gln)
13g.42606531T>CCA6967271TNFSF11c.567T>C (p.His189=)
c.426T>C (p.His142=)
c.348T>C (p.His116=)
c.405T>C (p.His135=)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
13g.42606531T>GCA388220861TNFSF11c.567T>G (p.His189Gln)
c.426T>G (p.His142Gln)
c.348T>G (p.His116Gln)
c.405T>G (p.His135Gln)
13g.42606531T=CA2087395051TNFSF11c.567T= (p.His189=)
c.426T= (p.His142=)
c.348T= (p.His116=)
c.405T= (p.His135=)
13g.42606532G>ACA388220864TNFSF11c.568G>A (p.Asp190Asn)
c.427G>A (p.Asp143Asn)
c.349G>A (p.Asp117Asn)
c.406G>A (p.Asp136Asn)
13g.42606532G>CCA388220866TNFSF11c.568G>C (p.Asp190His)
c.427G>C (p.Asp143His)
c.349G>C (p.Asp117His)
c.406G>C (p.Asp136His)
13g.42606532G>TCA388220868TNFSF11c.568G>T (p.Asp190Tyr)
c.427G>T (p.Asp143Tyr)
c.349G>T (p.Asp117Tyr)
c.406G>T (p.Asp136Tyr)
13g.42606533A=CA2087395052TNFSF11c.569A= (p.Asp190=)
c.428A= (p.Asp143=)
c.350A= (p.Asp117=)
c.407A= (p.Asp136=)
13g.42606533A>CCA388220871TNFSF11c.569A>C (p.Asp190Ala)
c.428A>C (p.Asp143Ala)
c.350A>C (p.Asp117Ala)
c.407A>C (p.Asp136Ala)
13g.42606533A>GCA388220873TNFSF11c.569A>G (p.Asp190Gly)
c.428A>G (p.Asp143Gly)
c.350A>G (p.Asp117Gly)
c.407A>G (p.Asp136Gly)
13g.42606533A>TCA6967272TNFSF11c.569A>T (p.Asp190Val)
c.428A>T (p.Asp143Val)
c.350A>T (p.Asp117Val)
c.407A>T (p.Asp136Val)
 dbSNP ExAC gnomAD v2
13g.42606534T>ACA388220876TNFSF11c.570T>A (p.Asp190Glu)
c.429T>A (p.Asp143Glu)
c.351T>A (p.Asp117Glu)
c.408T>A (p.Asp136Glu)
13g.42606534T>CCA483604999TNFSF11c.570T>C (p.Asp190=)
c.429T>C (p.Asp143=)
c.351T>C (p.Asp117=)
c.408T>C (p.Asp136=)
13g.42606534T>GCA249053394TNFSF11c.570T>G (p.Asp190Glu)
c.429T>G (p.Asp143Glu)
c.351T>G (p.Asp117Glu)
c.408T>G (p.Asp136Glu)
 dbSNP
13g.42606534T=CA2087395053TNFSF11c.570T= (p.Asp190=)
c.429T= (p.Asp143=)
c.351T= (p.Asp117=)
c.408T= (p.Asp136=)
13g.42606535C>ACA6967273TNFSF11c.571C>A (p.Arg191=)
c.430C>A (p.Arg144=)
c.352C>A (p.Arg118=)
c.409C>A (p.Arg137=)
 dbSNP ExAC gnomAD v2 gnomAD v4
13g.42606535C=CA2087395054TNFSF11c.571C= (p.Arg191=)
c.430C= (p.Arg144=)
c.352C= (p.Arg118=)
c.409C= (p.Arg137=)
13g.42606535C>GCA388220882TNFSF11c.571C>G (p.Arg191Gly)
c.430C>G (p.Arg144Gly)
c.352C>G (p.Arg118Gly)
c.409C>G (p.Arg137Gly)
 dbSNP
13g.42606535C>TCA6967274TNFSF11c.571C>T (p.Arg191Trp)
c.430C>T (p.Arg144Trp)
c.352C>T (p.Arg118Trp)
c.409C>T (p.Arg137Trp)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
13g.42606536G>ACA249053395TNFSF11c.572G>A (p.Arg191Gln)
c.431G>A (p.Arg144Gln)
c.353G>A (p.Arg118Gln)
c.410G>A (p.Arg137Gln)
 dbSNP gnomAD v4 COSMIC
13g.42606536G>CCA388220886TNFSF11c.572G>C (p.Arg191Pro)
c.431G>C (p.Arg144Pro)
c.353G>C (p.Arg118Pro)
c.410G>C (p.Arg137Pro)
13g.42606536G=CA2087395055TNFSF11c.572G= (p.Arg191=)
c.431G= (p.Arg144=)
c.353G= (p.Arg118=)
c.410G= (p.Arg137=)
13g.42606536G>TCA388220888TNFSF11c.572G>T (p.Arg191Leu)
c.431G>T (p.Arg144Leu)
c.353G>T (p.Arg118Leu)
c.410G>T (p.Arg137Leu)
13g.42606537G>ACA483605000TNFSF11c.573G>A (p.Arg191=)
c.432G>A (p.Arg144=)
c.354G>A (p.Arg118=)
c.411G>A (p.Arg137=)
 dbSNP gnomAD v2 gnomAD v4
13g.42606537G>CCA483605001TNFSF11c.573G>C (p.Arg191=)
c.432G>C (p.Arg144=)
c.354G>C (p.Arg118=)
c.411G>C (p.Arg137=)
13g.42606537G=CA2087395056TNFSF11c.573G= (p.Arg191=)
c.432G= (p.Arg144=)
c.354G= (p.Arg118=)
c.411G= (p.Arg137=)
13g.42606537G>TCA483605002TNFSF11c.573G>T (p.Arg191=)
c.432G>T (p.Arg144=)
c.354G>T (p.Arg118=)
c.411G>T (p.Arg137=)
13g.42606538G>ACA388220890TNFSF11c.574G>A (p.Gly192Ser)
c.433G>A (p.Gly145Ser)
c.355G>A (p.Gly119Ser)
c.412G>A (p.Gly138Ser)
13g.42606538G>CCA388220892TNFSF11c.574G>C (p.Gly192Arg)
c.433G>C (p.Gly145Arg)
c.355G>C (p.Gly119Arg)
c.412G>C (p.Gly138Arg)
13g.42606538G>TCA388220894TNFSF11c.574G>T (p.Gly192Cys)
c.433G>T (p.Gly145Cys)
c.355G>T (p.Gly119Cys)
c.412G>T (p.Gly138Cys)
13g.42606539G>ACA388220897TNFSF11c.575G>A (p.Gly192Asp)
c.434G>A (p.Gly145Asp)
c.356G>A (p.Gly119Asp)
c.413G>A (p.Gly138Asp)
13g.42606539G>CCA388220899TNFSF11c.575G>C (p.Gly192Ala)
c.434G>C (p.Gly145Ala)
c.356G>C (p.Gly119Ala)
c.413G>C (p.Gly138Ala)
13g.42606539G=CA2087395057TNFSF11c.575G= (p.Gly192=)
c.434G= (p.Gly145=)
c.356G= (p.Gly119=)
c.413G= (p.Gly138=)
13g.42606539G>TCA249053396TNFSF11c.575G>T (p.Gly192Val)
c.434G>T (p.Gly145Val)
c.356G>T (p.Gly119Val)
c.413G>T (p.Gly138Val)
 dbSNP
13g.42606540T>ACA483605003TNFSF11c.576T>A (p.Gly192=)
c.435T>A (p.Gly145=)
c.357T>A (p.Gly119=)
c.414T>A (p.Gly138=)
 gnomAD v4
13g.42606540T>CCA483605005TNFSF11c.576T>C (p.Gly192=)
c.435T>C (p.Gly145=)
c.357T>C (p.Gly119=)
c.414T>C (p.Gly138=)
 gnomAD v4
13g.42606540T>GCA483605004TNFSF11c.576T>G (p.Gly192=)
c.435T>G (p.Gly145=)
c.357T>G (p.Gly119=)
c.414T>G (p.Gly138=)
13g.42606541T>ACA388220903TNFSF11c.577T>A (p.Trp193Arg)
c.436T>A (p.Trp146Arg)
c.358T>A (p.Trp120Arg)
c.415T>A (p.Trp139Arg)
13g.42606541T>CCA388220904TNFSF11c.577T>C (p.Trp193Arg)
c.436T>C (p.Trp146Arg)
c.358T>C (p.Trp120Arg)
c.415T>C (p.Trp139Arg)
13g.42606541T>GCA388220906TNFSF11c.577T>G (p.Trp193Gly)
c.436T>G (p.Trp146Gly)
c.358T>G (p.Trp120Gly)
c.415T>G (p.Trp139Gly)
13g.42606542G>ACA388220913TNFSF11c.578G>A (p.Trp193Ter)
c.437G>A (p.Trp146Ter)
c.359G>A (p.Trp120Ter)
c.416G>A (p.Trp139Ter)
13g.42606542G>CCA388220910TNFSF11c.578G>C (p.Trp193Ser)
c.437G>C (p.Trp146Ser)
c.359G>C (p.Trp120Ser)
c.416G>C (p.Trp139Ser)
13g.42606542G>TCA388220909TNFSF11c.578G>T (p.Trp193Leu)
c.437G>T (p.Trp146Leu)
c.359G>T (p.Trp120Leu)
c.416G>T (p.Trp139Leu)
13g.42606544delCA2622837734TNFSF11c.580del (p.Ala194ProfsTer6)
c.439del (p.Ala147ProfsTer6)
c.361del (p.Ala121ProfsTer6)
c.418del (p.Ala140ProfsTer6)
 gnomAD v4
13g.42606543G>ACA388220915TNFSF11c.579G>A (p.Trp193Ter)
c.438G>A (p.Trp146Ter)
c.360G>A (p.Trp120Ter)
c.417G>A (p.Trp139Ter)
13g.42606543G>CCA388220919TNFSF11c.579G>C (p.Trp193Cys)
c.438G>C (p.Trp146Cys)
c.360G>C (p.Trp120Cys)
c.417G>C (p.Trp139Cys)
13g.42606543G>TCA388220917TNFSF11c.579G>T (p.Trp193Cys)
c.438G>T (p.Trp146Cys)
c.360G>T (p.Trp120Cys)
c.417G>T (p.Trp139Cys)
13g.42606544G>ACA388220921TNFSF11c.580G>A (p.Ala194Thr)
c.439G>A (p.Ala147Thr)
c.361G>A (p.Ala121Thr)
c.418G>A (p.Ala140Thr)
 dbSNP gnomAD v2 gnomAD v4
13g.42606544G>CCA388220923TNFSF11c.580G>C (p.Ala194Pro)
c.439G>C (p.Ala147Pro)
c.361G>C (p.Ala121Pro)
c.418G>C (p.Ala140Pro)
13g.42606544G=CA2087395058TNFSF11c.580G= (p.Ala194=)
c.439G= (p.Ala147=)
c.361G= (p.Ala121=)
c.418G= (p.Ala140=)
13g.42606544G>TCA388220926TNFSF11c.580G>T (p.Ala194Ser)
c.439G>T (p.Ala147Ser)
c.361G>T (p.Ala121Ser)
c.418G>T (p.Ala140Ser)
13g.42606545C>ACA388220928TNFSF11c.581C>A (p.Ala194Asp)
c.440C>A (p.Ala147Asp)
c.362C>A (p.Ala121Asp)
c.419C>A (p.Ala140Asp)
13g.42606545C>GCA388220930TNFSF11c.581C>G (p.Ala194Gly)
c.440C>G (p.Ala147Gly)
c.362C>G (p.Ala121Gly)
c.419C>G (p.Ala140Gly)
13g.42606545C>TCA388220932TNFSF11c.581C>T (p.Ala194Val)
c.440C>T (p.Ala147Val)
c.362C>T (p.Ala121Val)
c.419C>T (p.Ala140Val)
13g.42606546C>ACA483605008TNFSF11c.582C>A (p.Ala194=)
c.441C>A (p.Ala147=)
c.363C>A (p.Ala121=)
c.420C>A (p.Ala140=)
13g.42606546C>GCA483605009TNFSF11c.582C>G (p.Ala194=)
c.441C>G (p.Ala147=)
c.363C>G (p.Ala121=)
c.420C>G (p.Ala140=)
13g.42606546C>TCA483605010TNFSF11c.582C>T (p.Ala194=)
c.441C>T (p.Ala147=)
c.363C>T (p.Ala121=)
c.420C>T (p.Ala140=)
 gnomAD v4
13g.42606547A>CCA388220935TNFSF11c.583A>C (p.Lys195Gln)
c.442A>C (p.Lys148Gln)
c.364A>C (p.Lys122Gln)
c.421A>C (p.Lys141Gln)
13g.42606547A>GCA388220937TNFSF11c.583A>G (p.Lys195Glu)
c.442A>G (p.Lys148Glu)
c.364A>G (p.Lys122Glu)
c.421A>G (p.Lys141Glu)
13g.42606547A>TCA388220938TNFSF11c.583A>T (p.Lys195Ter)
c.442A>T (p.Lys148Ter)
c.364A>T (p.Lys122Ter)
c.421A>T (p.Lys141Ter)
13g.42606548A>CCA388220942TNFSF11c.584A>C (p.Lys195Thr)
c.443A>C (p.Lys148Thr)
c.365A>C (p.Lys122Thr)
c.422A>C (p.Lys141Thr)
13g.42606548A>GCA388220943TNFSF11c.584A>G (p.Lys195Arg)
c.443A>G (p.Lys148Arg)
c.365A>G (p.Lys122Arg)
c.422A>G (p.Lys141Arg)
13g.42606548A>TCA388220945TNFSF11c.584A>T (p.Lys195Met)
c.443A>T (p.Lys148Met)
c.365A>T (p.Lys122Met)
c.422A>T (p.Lys141Met)
13g.42606549G>ACA483605011TNFSF11c.585G>A (p.Lys195=)
c.444G>A (p.Lys148=)
c.366G>A (p.Lys122=)
c.423G>A (p.Lys141=)
13g.42606549G>CCA388220949TNFSF11c.585G>C (p.Lys195Asn)
c.444G>C (p.Lys148Asn)
c.366G>C (p.Lys122Asn)
c.423G>C (p.Lys141Asn)
 gnomAD v4
13g.42606549G>TCA388220948TNFSF11c.585G>T (p.Lys195Asn)
c.444G>T (p.Lys148Asn)
c.366G>T (p.Lys122Asn)
c.423G>T (p.Lys141Asn)
 COSMIC
13g.42606550A=CA2087395059TNFSF11c.586A= (p.Ile196=)
c.445A= (p.Ile149=)
c.367A= (p.Ile123=)
c.424A= (p.Ile142=)
13g.42606550A>CCA388220952TNFSF11c.586A>C (p.Ile196Leu)
c.445A>C (p.Ile149Leu)
c.367A>C (p.Ile123Leu)
c.424A>C (p.Ile142Leu)
13g.42606550A>GCA388220954TNFSF11c.586A>G (p.Ile196Val)
c.445A>G (p.Ile149Val)
c.367A>G (p.Ile123Val)
c.424A>G (p.Ile142Val)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
13g.42606550A>TCA388220956TNFSF11c.586A>T (p.Ile196Phe)
c.445A>T (p.Ile149Phe)
c.367A>T (p.Ile123Phe)
c.424A>T (p.Ile142Phe)
13g.42606551T>ACA388220958TNFSF11c.587T>A (p.Ile196Asn)
c.446T>A (p.Ile149Asn)
c.368T>A (p.Ile123Asn)
c.425T>A (p.Ile142Asn)
13g.42606551T>CCA388220960TNFSF11c.587T>C (p.Ile196Thr)
c.446T>C (p.Ile149Thr)
c.368T>C (p.Ile123Thr)
c.425T>C (p.Ile142Thr)
13g.42606551T>GCA388220961TNFSF11c.587T>G (p.Ile196Ser)
c.446T>G (p.Ile149Ser)
c.368T>G (p.Ile123Ser)
c.425T>G (p.Ile142Ser)
13g.42606552C>ACA483605012TNFSF11c.588C>A (p.Ile196=)
c.447C>A (p.Ile149=)
c.369C>A (p.Ile123=)
c.426C>A (p.Ile142=)
 gnomAD v4
13g.42606552C>GCA388220963TNFSF11c.588C>G (p.Ile196Met)
c.447C>G (p.Ile149Met)
c.369C>G (p.Ile123Met)
c.426C>G (p.Ile142Met)
13g.42606552C>TCA483605013TNFSF11c.588C>T (p.Ile196=)
c.447C>T (p.Ile149=)
c.369C>T (p.Ile123=)
c.426C>T (p.Ile142=)
 COSMIC
13g.42606553T>ACA388220966TNFSF11c.589T>A (p.Ser197Thr)
c.448T>A (p.Ser150Thr)
c.370T>A (p.Ser124Thr)
c.427T>A (p.Ser143Thr)
13g.42606553T>CCA388220967TNFSF11c.589T>C (p.Ser197Pro)
c.448T>C (p.Ser150Pro)
c.370T>C (p.Ser124Pro)
c.427T>C (p.Ser143Pro)
13g.42606553T>GCA388220970TNFSF11c.589T>G (p.Ser197Ala)
c.448T>G (p.Ser150Ala)
c.370T>G (p.Ser124Ala)
c.427T>G (p.Ser143Ala)
13g.42606554C>ACA388220972TNFSF11c.590C>A (p.Ser197Tyr)
c.449C>A (p.Ser150Tyr)
c.371C>A (p.Ser124Tyr)
c.428C>A (p.Ser143Tyr)
 gnomAD v4
13g.42606554C>GCA388220974TNFSF11c.590C>G (p.Ser197Cys)
c.449C>G (p.Ser150Cys)
c.371C>G (p.Ser124Cys)
c.428C>G (p.Ser143Cys)
 gnomAD v4
13g.42606554C>TCA388220976TNFSF11c.590C>T (p.Ser197Phe)
c.449C>T (p.Ser150Phe)
c.371C>T (p.Ser124Phe)
c.428C>T (p.Ser143Phe)
13g.42606555C>ACA246073TNFSF11c.591C>A (p.Ser197=)
c.450C>A (p.Ser150=)
c.372C>A (p.Ser124=)
c.429C>A (p.Ser143=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
13g.42606555C=CA2087395060TNFSF11c.591C= (p.Ser197=)
c.450C= (p.Ser150=)
c.372C= (p.Ser124=)
c.429C= (p.Ser143=)
13g.42606555C>GCA483605014TNFSF11c.591C>G (p.Ser197=)
c.450C>G (p.Ser150=)
c.372C>G (p.Ser124=)
c.429C>G (p.Ser143=)
13g.42606555C>TCA483605015TNFSF11c.591C>T (p.Ser197=)
c.450C>T (p.Ser150=)
c.372C>T (p.Ser124=)
c.429C>T (p.Ser143=)
13g.42606556A>CCA388220984TNFSF11c.592A>C (p.Asn198His)
c.451A>C (p.Asn151His)
c.373A>C (p.Asn125His)
c.430A>C (p.Asn144His)
13g.42606556A>GCA388220980TNFSF11c.592A>G (p.Asn198Asp)
c.451A>G (p.Asn151Asp)
c.373A>G (p.Asn125Asp)
c.430A>G (p.Asn144Asp)
13g.42606556A>TCA388220982TNFSF11c.592A>T (p.Asn198Tyr)
c.451A>T (p.Asn151Tyr)
c.373A>T (p.Asn125Tyr)
c.430A>T (p.Asn144Tyr)
13g.42606557A=CA2087395061TNFSF11c.593A= (p.Asn198=)
c.452A= (p.Asn151=)
c.374A= (p.Asn125=)
c.431A= (p.Asn144=)
13g.42606557A>CCA388220986TNFSF11c.593A>C (p.Asn198Thr)
c.452A>C (p.Asn151Thr)
c.374A>C (p.Asn125Thr)
c.431A>C (p.Asn144Thr)
13g.42606557A>GCA388220988TNFSF11c.593A>G (p.Asn198Ser)
c.452A>G (p.Asn151Ser)
c.374A>G (p.Asn125Ser)
c.431A>G (p.Asn144Ser)
 dbSNP gnomAD v3 gnomAD v4
13g.42606557A>TCA388220990TNFSF11c.593A>T (p.Asn198Ile)
c.452A>T (p.Asn151Ile)
c.374A>T (p.Asn125Ile)
c.431A>T (p.Asn144Ile)
13g.42606558C>ACA388220992TNFSF11c.594C>A (p.Asn198Lys)
c.453C>A (p.Asn151Lys)
c.375C>A (p.Asn125Lys)
c.432C>A (p.Asn144Lys)
13g.42606558C>GCA388220994TNFSF11c.594C>G (p.Asn198Lys)
c.453C>G (p.Asn151Lys)
c.375C>G (p.Asn125Lys)
c.432C>G (p.Asn144Lys)
13g.42606558C>TCA483605016TNFSF11c.594C>T (p.Asn198=)
c.453C>T (p.Asn151=)
c.375C>T (p.Asn125=)
c.432C>T (p.Asn144=)
13g.42606559A>CCA388220996TNFSF11c.595A>C (p.Met199Leu)
c.454A>C (p.Met152Leu)
c.376A>C (p.Met126Leu)
c.433A>C (p.Met145Leu)
13g.42606559A>GCA388220998TNFSF11c.595A>G (p.Met199Val)
c.454A>G (p.Met152Val)
c.376A>G (p.Met126Val)
c.433A>G (p.Met145Val)
 gnomAD v4
13g.42606559A>TCA388221001TNFSF11c.595A>T (p.Met199Leu)
c.454A>T (p.Met152Leu)
c.376A>T (p.Met126Leu)
c.433A>T (p.Met145Leu)
13g.42606560T>ACA118571TNFSF11c.596T>A (p.Met199Lys)
c.455T>A (p.Met152Lys)
c.377T>A (p.Met126Lys)
c.434T>A (p.Met145Lys)
 ClinVar dbSNP
13g.42606560T>CCA388221007TNFSF11c.596T>C (p.Met199Thr)
c.455T>C (p.Met152Thr)
c.377T>C (p.Met126Thr)
c.434T>C (p.Met145Thr)
13g.42606560T>GCA388221009TNFSF11c.596T>G (p.Met199Arg)
c.455T>G (p.Met152Arg)
c.377T>G (p.Met126Arg)
c.434T>G (p.Met145Arg)
13g.42606560T=CA2087395062TNFSF11c.596T= (p.Met199=)
c.455T= (p.Met152=)
c.377T= (p.Met126=)
c.434T= (p.Met145=)
13g.42606561G>ACA388221015TNFSF11c.597G>A (p.Met199Ile)
c.456G>A (p.Met152Ile)
c.378G>A (p.Met126Ile)
c.435G>A (p.Met145Ile)
13g.42606561G>CCA388221012TNFSF11c.597G>C (p.Met199Ile)
c.456G>C (p.Met152Ile)
c.378G>C (p.Met126Ile)
c.435G>C (p.Met145Ile)
13g.42606561G>TCA388221013TNFSF11c.597G>T (p.Met199Ile)
c.456G>T (p.Met152Ile)
c.378G>T (p.Met126Ile)
c.435G>T (p.Met145Ile)
13g.42606562A>CCA388221017TNFSF11c.598A>C (p.Thr200Pro)
c.457A>C (p.Thr153Pro)
c.379A>C (p.Thr127Pro)
c.436A>C (p.Thr146Pro)
13g.42606562A>GCA388221019TNFSF11c.598A>G (p.Thr200Ala)
c.457A>G (p.Thr153Ala)
c.379A>G (p.Thr127Ala)
c.436A>G (p.Thr146Ala)
13g.42606562A>TCA388221021TNFSF11c.598A>T (p.Thr200Ser)
c.457A>T (p.Thr153Ser)
c.379A>T (p.Thr127Ser)
c.436A>T (p.Thr146Ser)
13g.42606563C>ACA388221023TNFSF11c.599C>A (p.Thr200Asn)
c.458C>A (p.Thr153Asn)
c.380C>A (p.Thr127Asn)
c.437C>A (p.Thr146Asn)
13g.42606563C=CA2087395063TNFSF11c.599C= (p.Thr200=)
c.458C= (p.Thr153=)
c.380C= (p.Thr127=)
c.437C= (p.Thr146=)
13g.42606563C>GCA388221026TNFSF11c.599C>G (p.Thr200Ser)
c.458C>G (p.Thr153Ser)
c.380C>G (p.Thr127Ser)
c.437C>G (p.Thr146Ser)
13g.42606563C>TCA388221028TNFSF11c.599C>T (p.Thr200Ile)
c.458C>T (p.Thr153Ile)
c.380C>T (p.Thr127Ile)
c.437C>T (p.Thr146Ile)
 dbSNP gnomAD v3 gnomAD v4
13g.42606564T>ACA6967275TNFSF11c.600T>A (p.Thr200=)
c.459T>A (p.Thr153=)
c.381T>A (p.Thr127=)
c.438T>A (p.Thr146=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
13g.42606564T>CCA483605017TNFSF11c.600T>C (p.Thr200=)
c.459T>C (p.Thr153=)
c.381T>C (p.Thr127=)
c.438T>C (p.Thr146=)
13g.42606564T>GCA483605018TNFSF11c.600T>G (p.Thr200=)
c.459T>G (p.Thr153=)
c.381T>G (p.Thr127=)
c.438T>G (p.Thr146=)
13g.42606564T=CA2087395064TNFSF11c.600T= (p.Thr200=)
c.459T= (p.Thr153=)
c.381T= (p.Thr127=)
c.438T= (p.Thr146=)
13g.42606566_42606567delCA2622837735TNFSF11c.602_603del (p.Phe201Ter)
c.461_462del (p.Phe154Ter)
c.383_384del (p.Phe128Ter)
c.440_441del (p.Phe147Ter)
 gnomAD v4
13g.42606565T>ACA388221032TNFSF11c.601T>A (p.Phe201Ile)
c.460T>A (p.Phe154Ile)
c.382T>A (p.Phe128Ile)
c.439T>A (p.Phe147Ile)
13g.42606565T>CCA388221034TNFSF11c.601T>C (p.Phe201Leu)
c.460T>C (p.Phe154Leu)
c.382T>C (p.Phe128Leu)
c.439T>C (p.Phe147Leu)
13g.42606565T>GCA388221036TNFSF11c.601T>G (p.Phe201Val)
c.460T>G (p.Phe154Val)
c.382T>G (p.Phe128Val)
c.439T>G (p.Phe147Val)

Number of alleles fetched