| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 18 | g.62359956T>A | CA402613503 | TNFRSF11A | c.523T>A (p.Cys175Ser) n.441T>A c.481T>A (p.Cys161Ser) c.538T>A (p.Cys180Ser) c.415T>A (p.Cys139Ser) n.553T>A c.373T>A (p.Cys125Ser) c.313T>A (p.Cys105Ser) | |
| 18 | g.62359956T>C | CA118114 | TNFRSF11A | c.523T>C (p.Cys175Arg) n.441T>C c.481T>C (p.Cys161Arg) c.538T>C (p.Cys180Arg) c.415T>C (p.Cys139Arg) n.553T>C c.373T>C (p.Cys125Arg) c.313T>C (p.Cys105Arg) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 18 | g.62359956T>G | CA402613500 | TNFRSF11A | c.523T>G (p.Cys175Gly) n.441T>G c.481T>G (p.Cys161Gly) c.538T>G (p.Cys180Gly) c.415T>G (p.Cys139Gly) n.553T>G c.373T>G (p.Cys125Gly) c.313T>G (p.Cys105Gly) | |
| 18 | g.62359956T= | CA2308285215 | TNFRSF11A | c.523T= (p.Cys175=) n.441T= c.481T= (p.Cys161=) c.538T= (p.Cys180=) c.415T= (p.Cys139=) n.553T= c.373T= (p.Cys125=) c.313T= (p.Cys105=) | |
| 18 | g.62359957G>A | CA402613505 | TNFRSF11A | c.524G>A (p.Cys175Tyr) n.442G>A c.482G>A (p.Cys161Tyr) c.539G>A (p.Cys180Tyr) c.416G>A (p.Cys139Tyr) n.554G>A c.374G>A (p.Cys125Tyr) c.314G>A (p.Cys105Tyr) | gnomAD v4 |
| 18 | g.62359957G>C | CA402613506 | TNFRSF11A | c.524G>C (p.Cys175Ser) n.442G>C c.482G>C (p.Cys161Ser) c.539G>C (p.Cys180Ser) c.416G>C (p.Cys139Ser) n.554G>C c.374G>C (p.Cys125Ser) c.314G>C (p.Cys105Ser) | |
| 18 | g.62359957G>T | CA402613508 | TNFRSF11A | c.524G>T (p.Cys175Phe) n.442G>T c.482G>T (p.Cys161Phe) c.539G>T (p.Cys180Phe) c.416G>T (p.Cys139Phe) n.554G>T c.374G>T (p.Cys125Phe) c.314G>T (p.Cys105Phe) | |
| 18 | g.62359958T>A | CA402613510 | TNFRSF11A | c.525T>A (p.Cys175Ter) n.443T>A c.483T>A (p.Cys161Ter) c.540T>A (p.Cys180Ter) c.417T>A (p.Cys139Ter) n.555T>A c.375T>A (p.Cys125Ter) c.315T>A (p.Cys105Ter) | |
| 18 | g.62359958T>C | CA8983794 | TNFRSF11A | c.525T>C (p.Cys175=) n.443T>C c.483T>C (p.Cys161=) c.540T>C (p.Cys180=) c.417T>C (p.Cys139=) n.555T>C c.375T>C (p.Cys125=) c.315T>C (p.Cys105=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 18 | g.62359958T>G | CA402613511 | TNFRSF11A | c.525T>G (p.Cys175Trp) n.443T>G c.483T>G (p.Cys161Trp) c.540T>G (p.Cys180Trp) c.417T>G (p.Cys139Trp) n.555T>G c.375T>G (p.Cys125Trp) c.315T>G (p.Cys105Trp) | gnomAD v4 |
| 18 | g.62359958T= | CA2308285216 | TNFRSF11A | c.525T= (p.Cys175=) n.443T= c.483T= (p.Cys161=) c.540T= (p.Cys180=) c.417T= (p.Cys139=) n.555T= c.375T= (p.Cys125=) c.315T= (p.Cys105=) | |
| 18 | g.62359959A>C | CA402613517 | TNFRSF11A | c.526A>C (p.Thr176Pro) n.444A>C c.484A>C (p.Thr162Pro) c.541A>C (p.Thr181Pro) c.418A>C (p.Thr140Pro) n.556A>C c.376A>C (p.Thr126Pro) c.316A>C (p.Thr106Pro) | |
| 18 | g.62359959A>G | CA402613513 | TNFRSF11A | c.526A>G (p.Thr176Ala) n.444A>G c.484A>G (p.Thr162Ala) c.541A>G (p.Thr181Ala) c.418A>G (p.Thr140Ala) n.556A>G c.376A>G (p.Thr126Ala) c.316A>G (p.Thr106Ala) | |
| 18 | g.62359959A>T | CA402613515 | TNFRSF11A | c.526A>T (p.Thr176Ser) n.444A>T c.484A>T (p.Thr162Ser) c.541A>T (p.Thr181Ser) c.418A>T (p.Thr140Ser) n.556A>T c.376A>T (p.Thr126Ser) c.316A>T (p.Thr106Ser) | |
| 18 | g.62359960C>A | CA402613518 | TNFRSF11A | c.527C>A (p.Thr176Asn) n.445C>A c.485C>A (p.Thr162Asn) c.542C>A (p.Thr181Asn) c.419C>A (p.Thr140Asn) n.557C>A c.377C>A (p.Thr126Asn) c.317C>A (p.Thr106Asn) | |
| 18 | g.62359960C>G | CA402613519 | TNFRSF11A | c.527C>G (p.Thr176Ser) n.445C>G c.485C>G (p.Thr162Ser) c.542C>G (p.Thr181Ser) c.419C>G (p.Thr140Ser) n.557C>G c.377C>G (p.Thr126Ser) c.317C>G (p.Thr106Ser) | |
| 18 | g.62359960C>T | CA402613521 | TNFRSF11A | c.527C>T (p.Thr176Ile) n.445C>T c.485C>T (p.Thr162Ile) c.542C>T (p.Thr181Ile) c.419C>T (p.Thr140Ile) n.557C>T c.377C>T (p.Thr126Ile) c.317C>T (p.Thr106Ile) | gnomAD v4 |
| 18 | g.62359961C>A | CA504078914 | TNFRSF11A | c.528C>A (p.Thr176=) n.446C>A c.486C>A (p.Thr162=) c.543C>A (p.Thr181=) c.420C>A (p.Thr140=) n.558C>A c.378C>A (p.Thr126=) c.318C>A (p.Thr106=) | |
| 18 | g.62359961C>G | CA504078910 | TNFRSF11A | c.528C>G (p.Thr176=) n.446C>G c.486C>G (p.Thr162=) c.543C>G (p.Thr181=) c.420C>G (p.Thr140=) n.558C>G c.378C>G (p.Thr126=) c.318C>G (p.Thr106=) | |
| 18 | g.62359961C>T | CA504078911 | TNFRSF11A | c.528C>T (p.Thr176=) n.446C>T c.486C>T (p.Thr162=) c.543C>T (p.Thr181=) c.420C>T (p.Thr140=) n.558C>T c.378C>T (p.Thr126=) c.318C>T (p.Thr106=) | |
| 18 | g.62359962T>A | CA402613523 | TNFRSF11A | c.529T>A (p.Phe177Ile) n.447T>A c.487T>A (p.Phe163Ile) c.544T>A (p.Phe182Ile) c.421T>A (p.Phe141Ile) n.559T>A c.379T>A (p.Phe127Ile) c.319T>A (p.Phe107Ile) | |
| 18 | g.62359962T>C | CA402613525 | TNFRSF11A | c.529T>C (p.Phe177Leu) n.447T>C c.487T>C (p.Phe163Leu) c.544T>C (p.Phe182Leu) c.421T>C (p.Phe141Leu) n.559T>C c.379T>C (p.Phe127Leu) c.319T>C (p.Phe107Leu) | |
| 18 | g.62359962T>G | CA402613526 | TNFRSF11A | c.529T>G (p.Phe177Val) n.447T>G c.487T>G (p.Phe163Val) c.544T>G (p.Phe182Val) c.421T>G (p.Phe141Val) n.559T>G c.379T>G (p.Phe127Val) c.319T>G (p.Phe107Val) | |
| 18 | g.62359963T>A | CA402613531 | TNFRSF11A | c.530T>A (p.Phe177Tyr) n.448T>A c.488T>A (p.Phe163Tyr) c.545T>A (p.Phe182Tyr) c.422T>A (p.Phe141Tyr) n.560T>A c.380T>A (p.Phe127Tyr) c.320T>A (p.Phe107Tyr) | |
| 18 | g.62359963T>C | CA402613528 | TNFRSF11A | c.530T>C (p.Phe177Ser) n.448T>C c.488T>C (p.Phe163Ser) c.545T>C (p.Phe182Ser) c.422T>C (p.Phe141Ser) n.560T>C c.380T>C (p.Phe127Ser) c.320T>C (p.Phe107Ser) | ClinVar dbSNP gnomAD v4 |
| 18 | g.62359963T>G | CA402613530 | TNFRSF11A | c.530T>G (p.Phe177Cys) n.448T>G c.488T>G (p.Phe163Cys) c.545T>G (p.Phe182Cys) c.422T>G (p.Phe141Cys) n.560T>G c.380T>G (p.Phe127Cys) c.320T>G (p.Phe107Cys) | |
| 18 | g.62359963T= | CA2308285217 | TNFRSF11A | c.530T= (p.Phe177=) n.448T= c.488T= (p.Phe163=) c.545T= (p.Phe182=) c.422T= (p.Phe141=) n.560T= c.380T= (p.Phe127=) c.320T= (p.Phe107=) | |
| 18 | g.62359964C>A | CA402613533 | TNFRSF11A | c.531C>A (p.Phe177Leu) n.449C>A c.489C>A (p.Phe163Leu) c.546C>A (p.Phe182Leu) c.423C>A (p.Phe141Leu) n.561C>A c.381C>A (p.Phe127Leu) c.321C>A (p.Phe107Leu) | |
| 18 | g.62359964C>G | CA402613534 | TNFRSF11A | c.531C>G (p.Phe177Leu) n.449C>G c.489C>G (p.Phe163Leu) c.546C>G (p.Phe182Leu) c.423C>G (p.Phe141Leu) n.561C>G c.381C>G (p.Phe127Leu) c.321C>G (p.Phe107Leu) | |
| 18 | g.62359964C>T | CA504078923 | TNFRSF11A | c.531C>T (p.Phe177=) n.449C>T c.489C>T (p.Phe163=) c.546C>T (p.Phe182=) c.423C>T (p.Phe141=) n.561C>T c.381C>T (p.Phe127=) c.321C>T (p.Phe107=) | |
| 18 | g.62359965C>A | CA402613536 | TNFRSF11A | c.532C>A (p.Leu178Ile) n.450C>A c.490C>A (p.Leu164Ile) c.547C>A (p.Leu183Ile) c.424C>A (p.Leu142Ile) n.562C>A c.382C>A (p.Leu128Ile) c.322C>A (p.Leu108Ile) | |
| 18 | g.62359965C>G | CA402613538 | TNFRSF11A | c.532C>G (p.Leu178Val) n.450C>G c.490C>G (p.Leu164Val) c.547C>G (p.Leu183Val) c.424C>G (p.Leu142Val) n.562C>G c.382C>G (p.Leu128Val) c.322C>G (p.Leu108Val) | |
| 18 | g.62359965C>T | CA402613540 | TNFRSF11A | c.532C>T (p.Leu178Phe) n.450C>T c.490C>T (p.Leu164Phe) c.547C>T (p.Leu183Phe) c.424C>T (p.Leu142Phe) n.562C>T c.382C>T (p.Leu128Phe) c.322C>T (p.Leu108Phe) | |
| 18 | g.62359966T>A | CA402613541 | TNFRSF11A | c.533T>A (p.Leu178His) n.451T>A c.491T>A (p.Leu164His) c.548T>A (p.Leu183His) c.425T>A (p.Leu142His) n.563T>A c.383T>A (p.Leu128His) c.323T>A (p.Leu108His) | |
| 18 | g.62359966T>C | CA402613544 | TNFRSF11A | c.533T>C (p.Leu178Pro) n.451T>C c.491T>C (p.Leu164Pro) c.548T>C (p.Leu183Pro) c.425T>C (p.Leu142Pro) n.563T>C c.383T>C (p.Leu128Pro) c.323T>C (p.Leu108Pro) | |
| 18 | g.62359966T>G | CA402613543 | TNFRSF11A | c.533T>G (p.Leu178Arg) n.451T>G c.491T>G (p.Leu164Arg) c.548T>G (p.Leu183Arg) c.425T>G (p.Leu142Arg) n.563T>G c.383T>G (p.Leu128Arg) c.323T>G (p.Leu108Arg) | |
| 18 | g.62359967T>A | CA504078932 | TNFRSF11A | c.534T>A (p.Leu178=) n.452T>A c.492T>A (p.Leu164=) c.549T>A (p.Leu183=) c.426T>A (p.Leu142=) n.564T>A c.384T>A (p.Leu128=) c.324T>A (p.Leu108=) | |
| 18 | g.62359967T>C | CA504078934 | TNFRSF11A | c.534T>C (p.Leu178=) n.452T>C c.492T>C (p.Leu164=) c.549T>C (p.Leu183=) c.426T>C (p.Leu142=) n.564T>C c.384T>C (p.Leu128=) c.324T>C (p.Leu108=) | |
| 18 | g.62359967T>G | CA504078935 | TNFRSF11A | c.534T>G (p.Leu178=) n.452T>G c.492T>G (p.Leu164=) c.549T>G (p.Leu183=) c.426T>G (p.Leu142=) n.564T>G c.384T>G (p.Leu128=) c.324T>G (p.Leu108=) | |
| 18 | g.62359968G>A | CA10651299 | TNFRSF11A | c.535G>A (p.Gly179Arg) n.453G>A c.493G>A (p.Gly165Arg) c.550G>A (p.Gly184Arg) c.427G>A (p.Gly143Arg) n.565G>A c.385G>A (p.Gly129Arg) c.325G>A (p.Gly109Arg) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 18 | g.62359968G>C | CA402613546 | TNFRSF11A | c.535G>C (p.Gly179Arg) n.453G>C c.493G>C (p.Gly165Arg) c.550G>C (p.Gly184Arg) c.427G>C (p.Gly143Arg) n.565G>C c.385G>C (p.Gly129Arg) c.325G>C (p.Gly109Arg) | |
| 18 | g.62359968G= | CA2308285218 | TNFRSF11A | c.535G= (p.Gly179=) n.453G= c.493G= (p.Gly165=) c.550G= (p.Gly184=) c.427G= (p.Gly143=) n.565G= c.385G= (p.Gly129=) c.325G= (p.Gly109=) | |
| 18 | g.62359968G>T | CA402613547 | TNFRSF11A | c.535G>T (p.Gly179Ter) n.453G>T c.493G>T (p.Gly165Ter) c.550G>T (p.Gly184Ter) c.427G>T (p.Gly143Ter) n.565G>T c.385G>T (p.Gly129Ter) c.325G>T (p.Gly109Ter) | |
| 18 | g.62359969G>A | CA402613548 | TNFRSF11A | c.536G>A (p.Gly179Glu) n.454G>A c.494G>A (p.Gly165Glu) c.551G>A (p.Gly184Glu) c.428G>A (p.Gly143Glu) n.566G>A c.386G>A (p.Gly129Glu) c.326G>A (p.Gly109Glu) | |
| 18 | g.62359969G>C | CA402613550 | TNFRSF11A | c.536G>C (p.Gly179Ala) n.454G>C c.494G>C (p.Gly165Ala) c.551G>C (p.Gly184Ala) c.428G>C (p.Gly143Ala) n.566G>C c.386G>C (p.Gly129Ala) c.326G>C (p.Gly109Ala) | |
| 18 | g.62359969G>T | CA402613552 | TNFRSF11A | c.536G>T (p.Gly179Val) n.454G>T c.494G>T (p.Gly165Val) c.551G>T (p.Gly184Val) c.428G>T (p.Gly143Val) n.566G>T c.386G>T (p.Gly129Val) c.326G>T (p.Gly109Val) | |
| 18 | g.62359970A= | CA2308285219 | TNFRSF11A | c.537A= (p.Gly179=) n.455A= c.495A= (p.Gly165=) c.552A= (p.Gly184=) c.429A= (p.Gly143=) n.567A= c.387A= (p.Gly129=) c.327A= (p.Gly109=) | |
| 18 | g.62359970A>C | CA504078942 | TNFRSF11A | c.537A>C (p.Gly179=) n.455A>C c.495A>C (p.Gly165=) c.552A>C (p.Gly184=) c.429A>C (p.Gly143=) n.567A>C c.387A>C (p.Gly129=) c.327A>C (p.Gly109=) | |
| 18 | g.62359970A>G | CA504078944 | TNFRSF11A | c.537A>G (p.Gly179=) n.455A>G c.495A>G (p.Gly165=) c.552A>G (p.Gly184=) c.429A>G (p.Gly143=) n.567A>G c.387A>G (p.Gly129=) c.327A>G (p.Gly109=) | |
| 18 | g.62359970A>T | CA8983795 | TNFRSF11A | c.537A>T (p.Gly179=) n.455A>T c.495A>T (p.Gly165=) c.552A>T (p.Gly184=) c.429A>T (p.Gly143=) n.567A>T c.387A>T (p.Gly129=) c.327A>T (p.Gly109=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 18 | g.62359971A>C | CA402613554 | TNFRSF11A | c.538A>C (p.Lys180Gln) n.456A>C c.496A>C (p.Lys166Gln) c.553A>C (p.Lys185Gln) c.430A>C (p.Lys144Gln) n.568A>C c.388A>C (p.Lys130Gln) c.328A>C (p.Lys110Gln) | |
| 18 | g.62359971A>G | CA402613556 | TNFRSF11A | c.538A>G (p.Lys180Glu) n.456A>G c.496A>G (p.Lys166Glu) c.553A>G (p.Lys185Glu) c.430A>G (p.Lys144Glu) n.568A>G c.388A>G (p.Lys130Glu) c.328A>G (p.Lys110Glu) | |
| 18 | g.62359971A>T | CA402613558 | TNFRSF11A | c.538A>T (p.Lys180Ter) n.456A>T c.496A>T (p.Lys166Ter) c.553A>T (p.Lys185Ter) c.430A>T (p.Lys144Ter) n.568A>T c.388A>T (p.Lys130Ter) c.328A>T (p.Lys110Ter) | |
| 18 | g.62359972A>C | CA402613559 | TNFRSF11A | c.539A>C (p.Lys180Thr) n.457A>C c.497A>C (p.Lys166Thr) c.554A>C (p.Lys185Thr) c.431A>C (p.Lys144Thr) n.569A>C c.389A>C (p.Lys130Thr) c.329A>C (p.Lys110Thr) | |
| 18 | g.62359972A>G | CA402613561 | TNFRSF11A | c.539A>G (p.Lys180Arg) n.457A>G c.497A>G (p.Lys166Arg) c.554A>G (p.Lys185Arg) c.431A>G (p.Lys144Arg) n.569A>G c.389A>G (p.Lys130Arg) c.329A>G (p.Lys110Arg) | gnomAD v4 |
| 18 | g.62359972A>T | CA402613563 | TNFRSF11A | c.539A>T (p.Lys180Met) n.457A>T c.497A>T (p.Lys166Met) c.554A>T (p.Lys185Met) c.431A>T (p.Lys144Met) n.569A>T c.389A>T (p.Lys130Met) c.329A>T (p.Lys110Met) | |
| 18 | g.62359973G>A | CA504078952 | TNFRSF11A | c.540G>A (p.Lys180=) n.458G>A c.498G>A (p.Lys166=) c.555G>A (p.Lys185=) c.432G>A (p.Lys144=) n.570G>A c.390G>A (p.Lys130=) c.330G>A (p.Lys110=) | |
| 18 | g.62359973G>C | CA402613566 | TNFRSF11A | c.540G>C (p.Lys180Asn) n.458G>C c.498G>C (p.Lys166Asn) c.555G>C (p.Lys185Asn) c.432G>C (p.Lys144Asn) n.570G>C c.390G>C (p.Lys130Asn) c.330G>C (p.Lys110Asn) | |
| 18 | g.62359973G>T | CA402613565 | TNFRSF11A | c.540G>T (p.Lys180Asn) n.458G>T c.498G>T (p.Lys166Asn) c.555G>T (p.Lys185Asn) c.432G>T (p.Lys144Asn) n.570G>T c.390G>T (p.Lys130Asn) c.330G>T (p.Lys110Asn) | |
| 18 | g.62359974A>C | CA504078957 | TNFRSF11A | c.541A>C (p.Arg181=) n.459A>C c.499A>C (p.Arg167=) c.556A>C (p.Arg186=) c.433A>C (p.Arg145=) n.571A>C c.391A>C (p.Arg131=) c.331A>C (p.Arg111=) | |
| 18 | g.62359974A>G | CA402613567 | TNFRSF11A | c.541A>G (p.Arg181Gly) n.459A>G c.499A>G (p.Arg167Gly) c.556A>G (p.Arg186Gly) c.433A>G (p.Arg145Gly) n.571A>G c.391A>G (p.Arg131Gly) c.331A>G (p.Arg111Gly) | |
| 18 | g.62359974A>T | CA402613569 | TNFRSF11A | c.541A>T (p.Arg181Ter) n.459A>T c.499A>T (p.Arg167Ter) c.556A>T (p.Arg186Ter) c.433A>T (p.Arg145Ter) n.571A>T c.391A>T (p.Arg131Ter) c.331A>T (p.Arg111Ter) | |
| 18 | g.62359975G>A | CA402613571 | TNFRSF11A | c.542G>A (p.Arg181Lys) n.460G>A c.500G>A (p.Arg167Lys) c.557G>A (p.Arg186Lys) c.434G>A (p.Arg145Lys) n.572G>A c.392G>A (p.Arg131Lys) c.332G>A (p.Arg111Lys) | dbSNP |
| 18 | g.62359975G>C | CA402613572 | TNFRSF11A | c.542G>C (p.Arg181Thr) n.460G>C c.500G>C (p.Arg167Thr) c.557G>C (p.Arg186Thr) c.434G>C (p.Arg145Thr) n.572G>C c.392G>C (p.Arg131Thr) c.332G>C (p.Arg111Thr) | |
| 18 | g.62359975G= | CA2308285220 | TNFRSF11A | c.542G= (p.Arg181=) n.460G= c.500G= (p.Arg167=) c.557G= (p.Arg186=) c.434G= (p.Arg145=) n.572G= c.392G= (p.Arg131=) c.332G= (p.Arg111=) | |
| 18 | g.62359975G>T | CA402613574 | TNFRSF11A | c.542G>T (p.Arg181Ile) n.460G>T c.500G>T (p.Arg167Ile) c.557G>T (p.Arg186Ile) c.434G>T (p.Arg145Ile) n.572G>T c.392G>T (p.Arg131Ile) c.332G>T (p.Arg111Ile) | |
| 18 | g.62359976A= | CA2308285221 | TNFRSF11A | c.543A= (p.Arg181=) n.461A= c.501A= (p.Arg167=) c.558A= (p.Arg186=) c.435A= (p.Arg145=) n.573A= c.393A= (p.Arg131=) c.333A= (p.Arg111=) | |
| 18 | g.62359976A>C | CA402613576 | TNFRSF11A | c.543A>C (p.Arg181Ser) n.461A>C c.501A>C (p.Arg167Ser) c.558A>C (p.Arg186Ser) c.435A>C (p.Arg145Ser) n.573A>C c.393A>C (p.Arg131Ser) c.333A>C (p.Arg111Ser) | dbSNP gnomAD v3 gnomAD v4 |
| 18 | g.62359976A>G | CA504078963 | TNFRSF11A | c.543A>G (p.Arg181=) n.461A>G c.501A>G (p.Arg167=) c.558A>G (p.Arg186=) c.435A>G (p.Arg145=) n.573A>G c.393A>G (p.Arg131=) c.333A>G (p.Arg111=) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 18 | g.62359976A>T | CA8983796 | TNFRSF11A | c.543A>T (p.Arg181Ser) n.461A>T c.501A>T (p.Arg167Ser) c.558A>T (p.Arg186Ser) c.435A>T (p.Arg145Ser) n.573A>T c.393A>T (p.Arg131Ser) c.333A>T (p.Arg111Ser) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 18 | g.62359977G>A | CA402613579 | TNFRSF11A | c.544G>A (p.Val182Ile) n.462G>A c.502G>A (p.Val168Ile) c.559G>A (p.Val187Ile) c.436G>A (p.Val146Ile) n.574G>A c.394G>A (p.Val132Ile) c.334G>A (p.Val112Ile) | |
| 18 | g.62359977G>C | CA402613581 | TNFRSF11A | c.544G>C (p.Val182Leu) n.462G>C c.502G>C (p.Val168Leu) c.559G>C (p.Val187Leu) c.436G>C (p.Val146Leu) n.574G>C c.394G>C (p.Val132Leu) c.334G>C (p.Val112Leu) | |
| 18 | g.62359977G>T | CA402613582 | TNFRSF11A | c.544G>T (p.Val182Leu) n.462G>T c.502G>T (p.Val168Leu) c.559G>T (p.Val187Leu) c.436G>T (p.Val146Leu) n.574G>T c.394G>T (p.Val132Leu) c.334G>T (p.Val112Leu) | |
| 18 | g.62359978T>A | CA402613584 | TNFRSF11A | c.545T>A (p.Val182Glu) n.463T>A c.503T>A (p.Val168Glu) c.560T>A (p.Val187Glu) c.437T>A (p.Val146Glu) n.575T>A c.395T>A (p.Val132Glu) c.335T>A (p.Val112Glu) | |
| 18 | g.62359978T>C | CA402613586 | TNFRSF11A | c.545T>C (p.Val182Ala) n.463T>C c.503T>C (p.Val168Ala) c.560T>C (p.Val187Ala) c.437T>C (p.Val146Ala) n.575T>C c.395T>C (p.Val132Ala) c.335T>C (p.Val112Ala) | COSMIC |
| 18 | g.62359978T>G | CA402613588 | TNFRSF11A | c.545T>G (p.Val182Gly) n.463T>G c.503T>G (p.Val168Gly) c.560T>G (p.Val187Gly) c.437T>G (p.Val146Gly) n.575T>G c.395T>G (p.Val132Gly) c.335T>G (p.Val112Gly) | |
| 18 | g.62359979A>C | CA504078973 | TNFRSF11A | c.546A>C (p.Val182=) n.464A>C c.504A>C (p.Val168=) c.561A>C (p.Val187=) c.438A>C (p.Val146=) n.576A>C c.396A>C (p.Val132=) c.336A>C (p.Val112=) | |
| 18 | g.62359979A>G | CA504078974 | TNFRSF11A | c.546A>G (p.Val182=) n.464A>G c.504A>G (p.Val168=) c.561A>G (p.Val187=) c.438A>G (p.Val146=) n.576A>G c.396A>G (p.Val132=) c.336A>G (p.Val112=) | |
| 18 | g.62359979A>T | CA504078976 | TNFRSF11A | c.546A>T (p.Val182=) n.464A>T c.504A>T (p.Val168=) c.561A>T (p.Val187=) c.438A>T (p.Val146=) n.576A>T c.396A>T (p.Val132=) c.336A>T (p.Val112=) | |
| 18 | g.62359980G>A | CA402613590 | TNFRSF11A | c.547G>A (p.Glu183Lys) n.465G>A c.505G>A (p.Glu169Lys) c.562G>A (p.Glu188Lys) c.439G>A (p.Glu147Lys) n.577G>A c.397G>A (p.Glu133Lys) c.337G>A (p.Glu113Lys) | |
| 18 | g.62359980G>C | CA402613594 | TNFRSF11A | c.547G>C (p.Glu183Gln) n.465G>C c.505G>C (p.Glu169Gln) c.562G>C (p.Glu188Gln) c.439G>C (p.Glu147Gln) n.577G>C c.397G>C (p.Glu133Gln) c.337G>C (p.Glu113Gln) | gnomAD v4 COSMIC |
| 18 | g.62359980G>T | CA402613592 | TNFRSF11A | c.547G>T (p.Glu183Ter) n.465G>T c.505G>T (p.Glu169Ter) c.562G>T (p.Glu188Ter) c.439G>T (p.Glu147Ter) n.577G>T c.397G>T (p.Glu133Ter) c.337G>T (p.Glu113Ter) | |
| 18 | g.62359981A>C | CA402613596 | TNFRSF11A | c.548A>C (p.Glu183Ala) n.466A>C c.506A>C (p.Glu169Ala) c.563A>C (p.Glu188Ala) c.440A>C (p.Glu147Ala) n.578A>C c.398A>C (p.Glu133Ala) c.338A>C (p.Glu113Ala) | |
| 18 | g.62359981A>G | CA402613599 | TNFRSF11A | c.548A>G (p.Glu183Gly) n.466A>G c.506A>G (p.Glu169Gly) c.563A>G (p.Glu188Gly) c.440A>G (p.Glu147Gly) n.578A>G c.398A>G (p.Glu133Gly) c.338A>G (p.Glu113Gly) | |
| 18 | g.62359981A>T | CA402613597 | TNFRSF11A | c.548A>T (p.Glu183Val) n.466A>T c.506A>T (p.Glu169Val) c.563A>T (p.Glu188Val) c.440A>T (p.Glu147Val) n.578A>T c.398A>T (p.Glu133Val) c.338A>T (p.Glu113Val) | |
| 18 | g.62359982A>C | CA402613600 | TNFRSF11A | c.549A>C (p.Glu183Asp) n.467A>C c.507A>C (p.Glu169Asp) c.564A>C (p.Glu188Asp) c.441A>C (p.Glu147Asp) n.579A>C c.399A>C (p.Glu133Asp) c.339A>C (p.Glu113Asp) | |
| 18 | g.62359982A>G | CA504078986 | TNFRSF11A | c.549A>G (p.Glu183=) n.467A>G c.507A>G (p.Glu169=) c.564A>G (p.Glu188=) c.441A>G (p.Glu147=) n.579A>G c.399A>G (p.Glu133=) c.339A>G (p.Glu113=) | gnomAD v4 |
| 18 | g.62359982A>T | CA402613601 | TNFRSF11A | c.549A>T (p.Glu183Asp) n.467A>T c.507A>T (p.Glu169Asp) c.564A>T (p.Glu188Asp) c.441A>T (p.Glu147Asp) n.579A>T c.399A>T (p.Glu133Asp) c.339A>T (p.Glu113Asp) | |
| 18 | g.62359983C>A | CA402613603 | TNFRSF11A | c.550C>A (p.His184Asn) n.468C>A c.508C>A (p.His170Asn) c.565C>A (p.His189Asn) c.442C>A (p.His148Asn) n.580C>A c.400C>A (p.His134Asn) c.340C>A (p.His114Asn) | |
| 18 | g.62359983C= | CA2308285222 | TNFRSF11A | c.550C= (p.His184=) n.468C= c.508C= (p.His170=) c.565C= (p.His189=) c.442C= (p.His148=) n.580C= c.400C= (p.His134=) c.340C= (p.His114=) | |
| 18 | g.62359983C>G | CA402613605 | TNFRSF11A | c.550C>G (p.His184Asp) n.468C>G c.508C>G (p.His170Asp) c.565C>G (p.His189Asp) c.442C>G (p.His148Asp) n.580C>G c.400C>G (p.His134Asp) c.340C>G (p.His114Asp) | |
| 18 | g.62359983C>T | CA8983797 | TNFRSF11A | c.550C>T (p.His184Tyr) n.468C>T c.508C>T (p.His170Tyr) c.565C>T (p.His189Tyr) c.442C>T (p.His148Tyr) n.580C>T c.400C>T (p.His134Tyr) c.340C>T (p.His114Tyr) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 18 | g.62359984A= | CA2308285223 | TNFRSF11A | c.551A= (p.His184=) n.469A= c.509A= (p.His170=) c.566A= (p.His189=) c.443A= (p.His148=) n.581A= c.401A= (p.His134=) c.341A= (p.His114=) | |
| 18 | g.62359984A>C | CA402613607 | TNFRSF11A | c.551A>C (p.His184Pro) n.469A>C c.509A>C (p.His170Pro) c.566A>C (p.His189Pro) c.443A>C (p.His148Pro) n.581A>C c.401A>C (p.His134Pro) c.341A>C (p.His114Pro) | |
| 18 | g.62359984A>G | CA402613608 | TNFRSF11A | c.551A>G (p.His184Arg) n.469A>G c.509A>G (p.His170Arg) c.566A>G (p.His189Arg) c.443A>G (p.His148Arg) n.581A>G c.401A>G (p.His134Arg) c.341A>G (p.His114Arg) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 18 | g.62359984A>T | CA402613609 | TNFRSF11A | c.551A>T (p.His184Leu) n.469A>T c.509A>T (p.His170Leu) c.566A>T (p.His189Leu) c.443A>T (p.His148Leu) n.581A>T c.401A>T (p.His134Leu) c.341A>T (p.His114Leu) | |
| 18 | g.62359985T>A | CA402613612 | TNFRSF11A | c.552T>A (p.His184Gln) n.470T>A c.510T>A (p.His170Gln) c.567T>A (p.His189Gln) c.444T>A (p.His148Gln) n.582T>A c.402T>A (p.His134Gln) c.342T>A (p.His114Gln) | |
| 18 | g.62359985T>C | CA504078995 | TNFRSF11A | c.552T>C (p.His184=) n.470T>C c.510T>C (p.His170=) c.567T>C (p.His189=) c.444T>C (p.His148=) n.582T>C c.402T>C (p.His134=) c.342T>C (p.His114=) | |
| 18 | g.62359985T>G | CA402613613 | TNFRSF11A | c.552T>G (p.His184Gln) n.470T>G c.510T>G (p.His170Gln) c.567T>G (p.His189Gln) c.444T>G (p.His148Gln) n.582T>G c.402T>G (p.His134Gln) c.342T>G (p.His114Gln) | |
| 18 | g.62359986C>A | CA402613618 | TNFRSF11A | c.553C>A (p.His185Asn) n.471C>A c.511C>A (p.His171Asn) c.568C>A (p.His190Asn) c.445C>A (p.His149Asn) n.583C>A c.403C>A (p.His135Asn) c.343C>A (p.His115Asn) | |
| 18 | g.62359986C>G | CA402613616 | TNFRSF11A | c.553C>G (p.His185Asp) n.471C>G c.511C>G (p.His171Asp) c.568C>G (p.His190Asp) c.445C>G (p.His149Asp) n.583C>G c.403C>G (p.His135Asp) c.343C>G (p.His115Asp) | |
| 18 | g.62359986C>T | CA402613615 | TNFRSF11A | c.553C>T (p.His185Tyr) n.471C>T c.511C>T (p.His171Tyr) c.568C>T (p.His190Tyr) c.445C>T (p.His149Tyr) n.583C>T c.403C>T (p.His135Tyr) c.343C>T (p.His115Tyr) | |
| 18 | g.62359987A= | CA2308285224 | TNFRSF11A | c.554A= (p.His185=) n.472A= c.512A= (p.His171=) c.569A= (p.His190=) c.446A= (p.His149=) n.584A= c.404A= (p.His135=) c.344A= (p.His115=) | |
| 18 | g.62359987A>C | CA402613620 | TNFRSF11A | c.554A>C (p.His185Pro) n.472A>C c.512A>C (p.His171Pro) c.569A>C (p.His190Pro) c.446A>C (p.His149Pro) n.584A>C c.404A>C (p.His135Pro) c.344A>C (p.His115Pro) | |
| 18 | g.62359987A>G | CA402613622 | TNFRSF11A | c.554A>G (p.His185Arg) n.472A>G c.512A>G (p.His171Arg) c.569A>G (p.His190Arg) c.446A>G (p.His149Arg) n.584A>G c.404A>G (p.His135Arg) c.344A>G (p.His115Arg) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 18 | g.62359987A>T | CA402613624 | TNFRSF11A | c.554A>T (p.His185Leu) n.472A>T c.512A>T (p.His171Leu) c.569A>T (p.His190Leu) c.446A>T (p.His149Leu) n.584A>T c.404A>T (p.His135Leu) c.344A>T (p.His115Leu) | |
| 18 | g.62359988T>A | CA402613625 | TNFRSF11A | c.555T>A (p.His185Gln) n.473T>A c.513T>A (p.His171Gln) c.570T>A (p.His190Gln) c.447T>A (p.His149Gln) n.585T>A c.405T>A (p.His135Gln) c.345T>A (p.His115Gln) | |
| 18 | g.62359988T>C | CA8983798 | TNFRSF11A | c.555T>C (p.His185=) n.473T>C c.513T>C (p.His171=) c.570T>C (p.His190=) c.447T>C (p.His149=) n.585T>C c.405T>C (p.His135=) c.345T>C (p.His115=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 18 | g.62359988T>G | CA402613627 | TNFRSF11A | c.555T>G (p.His185Gln) n.473T>G c.513T>G (p.His171Gln) c.570T>G (p.His190Gln) c.447T>G (p.His149Gln) n.585T>G c.405T>G (p.His135Gln) c.345T>G (p.His115Gln) | |
| 18 | g.62359988T= | CA2308285225 | TNFRSF11A | c.555T= (p.His185=) n.473T= c.513T= (p.His171=) c.570T= (p.His190=) c.447T= (p.His149=) n.585T= c.405T= (p.His135=) c.345T= (p.His115=) | |
| 18 | g.62359989G>A | CA402613630 | TNFRSF11A | c.556G>A (p.Gly186Arg) n.474G>A c.514G>A (p.Gly172Arg) c.571G>A (p.Gly191Arg) c.448G>A (p.Gly150Arg) n.586G>A c.406G>A (p.Gly136Arg) c.346G>A (p.Gly116Arg) | |
| 18 | g.62359989G>C | CA402613633 | TNFRSF11A | c.556G>C (p.Gly186Arg) n.474G>C c.514G>C (p.Gly172Arg) c.571G>C (p.Gly191Arg) c.448G>C (p.Gly150Arg) n.586G>C c.406G>C (p.Gly136Arg) c.346G>C (p.Gly116Arg) | |
| 18 | g.62359989G>T | CA402613634 | TNFRSF11A | c.556G>T (p.Gly186Trp) n.474G>T c.514G>T (p.Gly172Trp) c.571G>T (p.Gly191Trp) c.448G>T (p.Gly150Trp) n.586G>T c.406G>T (p.Gly136Trp) c.346G>T (p.Gly116Trp) | |
| 18 | g.62359990_62359991del | CA2812750092 | TNFRSF11A | c.557_558del (p.Gly186AspfsTer15) n.475_476del c.515_516del (p.Gly172AspfsTer15) c.572_573del (p.Gly191AspfsTer15) c.449_450del (p.Gly150AspfsTer15) n.587_588del c.407_408del (p.Gly136AspfsTer15) c.347_348del (p.Gly116AspfsTer15) | |
| 18 | g.62359990G>A | CA402613635 | TNFRSF11A | c.557G>A (p.Gly186Glu) n.475G>A c.515G>A (p.Gly172Glu) c.572G>A (p.Gly191Glu) c.449G>A (p.Gly150Glu) n.587G>A c.407G>A (p.Gly136Glu) c.347G>A (p.Gly116Glu) | |
| 18 | g.62359990G>C | CA402613637 | TNFRSF11A | c.557G>C (p.Gly186Ala) n.475G>C c.515G>C (p.Gly172Ala) c.572G>C (p.Gly191Ala) c.449G>C (p.Gly150Ala) n.587G>C c.407G>C (p.Gly136Ala) c.347G>C (p.Gly116Ala) | |
| 18 | g.62359990G>T | CA402613638 | TNFRSF11A | c.557G>T (p.Gly186Val) n.475G>T c.515G>T (p.Gly172Val) c.572G>T (p.Gly191Val) c.449G>T (p.Gly150Val) n.587G>T c.407G>T (p.Gly136Val) c.347G>T (p.Gly116Val) | |
| 18 | g.62359991G>A | CA504079011 | TNFRSF11A | c.558G>A (p.Gly186=) n.476G>A c.516G>A (p.Gly172=) c.573G>A (p.Gly191=) c.450G>A (p.Gly150=) n.588G>A c.408G>A (p.Gly136=) c.348G>A (p.Gly116=) | |
| 18 | g.62359991G>C | CA504079013 | TNFRSF11A | c.558G>C (p.Gly186=) n.476G>C c.516G>C (p.Gly172=) c.573G>C (p.Gly191=) c.450G>C (p.Gly150=) n.588G>C c.408G>C (p.Gly136=) c.348G>C (p.Gly116=) | |
| 18 | g.62359991G>T | CA504079014 | TNFRSF11A | c.558G>T (p.Gly186=) n.476G>T c.516G>T (p.Gly172=) c.573G>T (p.Gly191=) c.450G>T (p.Gly150=) n.588G>T c.408G>T (p.Gly136=) c.348G>T (p.Gly116=) | dbSNP |
| 18 | g.62359992A>C | CA402613642 | TNFRSF11A | c.559A>C (p.Thr187Pro) n.477A>C c.517A>C (p.Thr173Pro) c.574A>C (p.Thr192Pro) c.451A>C (p.Thr151Pro) n.589A>C c.409A>C (p.Thr137Pro) c.349A>C (p.Thr117Pro) | |
| 18 | g.62359992A>G | CA402613644 | TNFRSF11A | c.559A>G (p.Thr187Ala) n.477A>G c.517A>G (p.Thr173Ala) c.574A>G (p.Thr192Ala) c.451A>G (p.Thr151Ala) n.589A>G c.409A>G (p.Thr137Ala) c.349A>G (p.Thr117Ala) | COSMIC |
| 18 | g.62359992A>T | CA402613640 | TNFRSF11A | c.559A>T (p.Thr187Ser) n.477A>T c.517A>T (p.Thr173Ser) c.574A>T (p.Thr192Ser) c.451A>T (p.Thr151Ser) n.589A>T c.409A>T (p.Thr137Ser) c.349A>T (p.Thr117Ser) | |
| 18 | g.62359993C>A | CA402613645 | TNFRSF11A | c.560C>A (p.Thr187Lys) n.478C>A c.518C>A (p.Thr173Lys) c.575C>A (p.Thr192Lys) c.452C>A (p.Thr151Lys) n.590C>A c.410C>A (p.Thr137Lys) c.350C>A (p.Thr117Lys) | |
| 18 | g.62359993C= | CA2308285226 | TNFRSF11A | c.560C= (p.Thr187=) n.478C= c.518C= (p.Thr173=) c.575C= (p.Thr192=) c.452C= (p.Thr151=) n.590C= c.410C= (p.Thr137=) c.350C= (p.Thr117=) | |
| 18 | g.62359993C>G | CA402613646 | TNFRSF11A | c.560C>G (p.Thr187Arg) n.478C>G c.518C>G (p.Thr173Arg) c.575C>G (p.Thr192Arg) c.452C>G (p.Thr151Arg) n.590C>G c.410C>G (p.Thr137Arg) c.350C>G (p.Thr117Arg) | dbSNP gnomAD v2 gnomAD v4 |
| 18 | g.62359993C>T | CA402613648 | TNFRSF11A | c.560C>T (p.Thr187Ile) n.478C>T c.518C>T (p.Thr173Ile) c.575C>T (p.Thr192Ile) c.452C>T (p.Thr151Ile) n.590C>T c.410C>T (p.Thr137Ile) c.350C>T (p.Thr117Ile) | dbSNP |
| 18 | g.62359994A= | CA2308285227 | TNFRSF11A | c.561A= (p.Thr187=) n.479A= c.519A= (p.Thr173=) c.576A= (p.Thr192=) c.453A= (p.Thr151=) n.591A= c.411A= (p.Thr137=) c.351A= (p.Thr117=) | |
| 18 | g.62359994A>C | CA504079023 | TNFRSF11A | c.561A>C (p.Thr187=) n.479A>C c.519A>C (p.Thr173=) c.576A>C (p.Thr192=) c.453A>C (p.Thr151=) n.591A>C c.411A>C (p.Thr137=) c.351A>C (p.Thr117=) | dbSNP gnomAD v3 gnomAD v4 |
| 18 | g.62359994A>G | CA504079026 | TNFRSF11A | c.561A>G (p.Thr187=) n.479A>G c.519A>G (p.Thr173=) c.576A>G (p.Thr192=) c.453A>G (p.Thr151=) n.591A>G c.411A>G (p.Thr137=) c.351A>G (p.Thr117=) | |
| 18 | g.62359994A>T | CA504079024 | TNFRSF11A | c.561A>T (p.Thr187=) n.479A>T c.519A>T (p.Thr173=) c.576A>T (p.Thr192=) c.453A>T (p.Thr151=) n.591A>T c.411A>T (p.Thr137=) c.351A>T (p.Thr117=) | |
| 18 | g.62359995G>A | CA402613651 | TNFRSF11A | c.562G>A (p.Glu188Lys) n.480G>A c.520G>A (p.Glu174Lys) c.577G>A (p.Glu193Lys) c.454G>A (p.Glu152Lys) n.592G>A c.412G>A (p.Glu138Lys) c.352G>A (p.Glu118Lys) | COSMIC |
| 18 | g.62359995G>C | CA402613652 | TNFRSF11A | c.562G>C (p.Glu188Gln) n.480G>C c.520G>C (p.Glu174Gln) c.577G>C (p.Glu193Gln) c.454G>C (p.Glu152Gln) n.592G>C c.412G>C (p.Glu138Gln) c.352G>C (p.Glu118Gln) | |
| 18 | g.62359995G>T | CA402613654 | TNFRSF11A | c.562G>T (p.Glu188Ter) n.480G>T c.520G>T (p.Glu174Ter) c.577G>T (p.Glu193Ter) c.454G>T (p.Glu152Ter) n.592G>T c.412G>T (p.Glu138Ter) c.352G>T (p.Glu118Ter) | |
| 18 | g.62359996A>C | CA402613660 | TNFRSF11A | c.563A>C (p.Glu188Ala) n.481A>C c.521A>C (p.Glu174Ala) c.578A>C (p.Glu193Ala) c.455A>C (p.Glu152Ala) n.593A>C c.413A>C (p.Glu138Ala) c.353A>C (p.Glu118Ala) | |
| 18 | g.62359996A>G | CA402613657 | TNFRSF11A | c.563A>G (p.Glu188Gly) n.481A>G c.521A>G (p.Glu174Gly) c.578A>G (p.Glu193Gly) c.455A>G (p.Glu152Gly) n.593A>G c.413A>G (p.Glu138Gly) c.353A>G (p.Glu118Gly) | gnomAD v4 |
| 18 | g.62359996A>T | CA402613658 | TNFRSF11A | c.563A>T (p.Glu188Val) n.481A>T c.521A>T (p.Glu174Val) c.578A>T (p.Glu193Val) c.455A>T (p.Glu152Val) n.593A>T c.413A>T (p.Glu138Val) c.353A>T (p.Glu118Val) | |
| 18 | g.62359997G>A | CA504079034 | TNFRSF11A | c.564G>A (p.Glu188=) n.482G>A c.522G>A (p.Glu174=) c.579G>A (p.Glu193=) c.456G>A (p.Glu152=) n.594G>A c.414G>A (p.Glu138=) c.354G>A (p.Glu118=) | |
| 18 | g.62359997G>C | CA402613661 | TNFRSF11A | c.564G>C (p.Glu188Asp) n.482G>C c.522G>C (p.Glu174Asp) c.579G>C (p.Glu193Asp) c.456G>C (p.Glu152Asp) n.594G>C c.414G>C (p.Glu138Asp) c.354G>C (p.Glu118Asp) | |
| 18 | g.62359997G>T | CA402613663 | TNFRSF11A | c.564G>T (p.Glu188Asp) n.482G>T c.522G>T (p.Glu174Asp) c.579G>T (p.Glu193Asp) c.456G>T (p.Glu152Asp) n.594G>T c.414G>T (p.Glu138Asp) c.354G>T (p.Glu118Asp) | |
| 18 | g.62359998A>C | CA402613665 | TNFRSF11A | c.565A>C (p.Lys189Gln) n.483A>C c.523A>C (p.Lys175Gln) c.580A>C (p.Lys194Gln) c.457A>C (p.Lys153Gln) n.595A>C c.415A>C (p.Lys139Gln) c.355A>C (p.Lys119Gln) | |
| 18 | g.62359998A>G | CA402613667 | TNFRSF11A | c.565A>G (p.Lys189Glu) n.483A>G c.523A>G (p.Lys175Glu) c.580A>G (p.Lys194Glu) c.457A>G (p.Lys153Glu) n.595A>G c.415A>G (p.Lys139Glu) c.355A>G (p.Lys119Glu) | |
| 18 | g.62359998A>T | CA402613669 | TNFRSF11A | c.565A>T (p.Lys189Ter) n.483A>T c.523A>T (p.Lys175Ter) c.580A>T (p.Lys194Ter) c.457A>T (p.Lys153Ter) n.595A>T c.415A>T (p.Lys139Ter) c.355A>T (p.Lys119Ter) | |
| 18 | g.62359999A>C | CA402613671 | TNFRSF11A | c.566A>C (p.Lys189Thr) n.484A>C c.524A>C (p.Lys175Thr) c.581A>C (p.Lys194Thr) c.458A>C (p.Lys153Thr) n.596A>C c.416A>C (p.Lys139Thr) c.356A>C (p.Lys119Thr) | |
| 18 | g.62359999A>G | CA402613674 | TNFRSF11A | c.566A>G (p.Lys189Arg) n.484A>G c.524A>G (p.Lys175Arg) c.581A>G (p.Lys194Arg) c.458A>G (p.Lys153Arg) n.596A>G c.416A>G (p.Lys139Arg) c.356A>G (p.Lys119Arg) | |
| 18 | g.62359999A>T | CA402613672 | TNFRSF11A | c.566A>T (p.Lys189Ile) n.484A>T c.524A>T (p.Lys175Ile) c.581A>T (p.Lys194Ile) c.458A>T (p.Lys153Ile) n.596A>T c.416A>T (p.Lys139Ile) c.356A>T (p.Lys119Ile) | gnomAD v4 |
| 18 | g.62360000A= | CA2308285228 | TNFRSF11A | c.567A= (p.Lys189=) n.485A= c.525A= (p.Lys175=) c.582A= (p.Lys194=) c.459A= (p.Lys153=) n.597A= c.417A= (p.Lys139=) c.357A= (p.Lys119=) | |
| 18 | g.62360000A>C | CA402613675 | TNFRSF11A | c.567A>C (p.Lys189Asn) n.485A>C c.525A>C (p.Lys175Asn) c.582A>C (p.Lys194Asn) c.459A>C (p.Lys153Asn) n.597A>C c.417A>C (p.Lys139Asn) c.357A>C (p.Lys119Asn) | |
| 18 | g.62360000A>G | CA301697937 | TNFRSF11A | c.567A>G (p.Lys189=) n.485A>G c.525A>G (p.Lys175=) c.582A>G (p.Lys194=) c.459A>G (p.Lys153=) n.597A>G c.417A>G (p.Lys139=) c.357A>G (p.Lys119=) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 18 | g.62360000A>T | CA402613676 | TNFRSF11A | c.567A>T (p.Lys189Asn) n.485A>T c.525A>T (p.Lys175Asn) c.582A>T (p.Lys194Asn) c.459A>T (p.Lys153Asn) n.597A>T c.417A>T (p.Lys139Asn) c.357A>T (p.Lys119Asn) | |
| 18 | g.62360001T>A | CA402613678 | TNFRSF11A | c.568T>A (p.Ser190Thr) n.486T>A c.526T>A (p.Ser176Thr) c.583T>A (p.Ser195Thr) c.460T>A (p.Ser154Thr) n.598T>A c.418T>A (p.Ser140Thr) c.358T>A (p.Ser120Thr) | gnomAD v4 |
| 18 | g.62360001T>C | CA402613680 | TNFRSF11A | c.568T>C (p.Ser190Pro) n.486T>C c.526T>C (p.Ser176Pro) c.583T>C (p.Ser195Pro) c.460T>C (p.Ser154Pro) n.598T>C c.418T>C (p.Ser140Pro) c.358T>C (p.Ser120Pro) | gnomAD v4 |
| 18 | g.62360001T>G | CA402613681 | TNFRSF11A | c.568T>G (p.Ser190Ala) n.486T>G c.526T>G (p.Ser176Ala) c.583T>G (p.Ser195Ala) c.460T>G (p.Ser154Ala) n.598T>G c.418T>G (p.Ser140Ala) c.358T>G (p.Ser120Ala) | |
| 18 | g.62360002C>A | CA402613684 | TNFRSF11A | c.569C>A (p.Ser190Tyr) n.487C>A c.527C>A (p.Ser176Tyr) c.584C>A (p.Ser195Tyr) c.461C>A (p.Ser154Tyr) n.599C>A c.419C>A (p.Ser140Tyr) c.359C>A (p.Ser120Tyr) | |
| 18 | g.62360002C= | CA2308285229 | TNFRSF11A | c.569C= (p.Ser190=) n.487C= c.527C= (p.Ser176=) c.584C= (p.Ser195=) c.461C= (p.Ser154=) n.599C= c.419C= (p.Ser140=) c.359C= (p.Ser120=) | |
| 18 | g.62360002C>G | CA402613685 | TNFRSF11A | c.569C>G (p.Ser190Cys) n.487C>G c.527C>G (p.Ser176Cys) c.584C>G (p.Ser195Cys) c.461C>G (p.Ser154Cys) n.599C>G c.419C>G (p.Ser140Cys) c.359C>G (p.Ser120Cys) | |
| 18 | g.62360002C>T | CA8983799 | TNFRSF11A | c.569C>T (p.Ser190Phe) n.487C>T c.527C>T (p.Ser176Phe) c.584C>T (p.Ser195Phe) c.461C>T (p.Ser154Phe) n.599C>T c.419C>T (p.Ser140Phe) c.359C>T (p.Ser120Phe) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 18 | g.62360003C>A | CA504079055 | TNFRSF11A | c.570C>A (p.Ser190=) n.488C>A c.528C>A (p.Ser176=) c.585C>A (p.Ser195=) c.462C>A (p.Ser154=) n.600C>A c.420C>A (p.Ser140=) c.360C>A (p.Ser120=) | |
| 18 | g.62360003C= | CA2308285230 | TNFRSF11A | c.570C= (p.Ser190=) n.488C= c.528C= (p.Ser176=) c.585C= (p.Ser195=) c.462C= (p.Ser154=) n.600C= c.420C= (p.Ser140=) c.360C= (p.Ser120=) | |
| 18 | g.62360003C>G | CA504079053 | TNFRSF11A | c.570C>G (p.Ser190=) n.488C>G c.528C>G (p.Ser176=) c.585C>G (p.Ser195=) c.462C>G (p.Ser154=) n.600C>G c.420C>G (p.Ser140=) c.360C>G (p.Ser120=) | |
| 18 | g.62360003C>T | CA8983800 | TNFRSF11A | c.570C>T (p.Ser190=) n.488C>T c.528C>T (p.Ser176=) c.585C>T (p.Ser195=) c.462C>T (p.Ser154=) n.600C>T c.420C>T (p.Ser140=) c.360C>T (p.Ser120=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 18 | g.62360004G>A | CA8983801 | TNFRSF11A | c.571G>A (p.Asp191Asn) n.489G>A c.529G>A (p.Asp177Asn) c.586G>A (p.Asp196Asn) c.463G>A (p.Asp155Asn) n.601G>A c.421G>A (p.Asp141Asn) c.361G>A (p.Asp121Asn) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 18 | g.62360004G>C | CA402613690 | TNFRSF11A | c.571G>C (p.Asp191His) n.489G>C c.529G>C (p.Asp177His) c.586G>C (p.Asp196His) c.463G>C (p.Asp155His) n.601G>C c.421G>C (p.Asp141His) c.361G>C (p.Asp121His) | |
| 18 | g.62360004G= | CA2308285231 | TNFRSF11A | c.571G= (p.Asp191=) n.489G= c.529G= (p.Asp177=) c.586G= (p.Asp196=) c.463G= (p.Asp155=) n.601G= c.421G= (p.Asp141=) c.361G= (p.Asp121=) | |
| 18 | g.62360004G>T | CA402613692 | TNFRSF11A | c.571G>T (p.Asp191Tyr) n.489G>T c.529G>T (p.Asp177Tyr) c.586G>T (p.Asp196Tyr) c.463G>T (p.Asp155Tyr) n.601G>T c.421G>T (p.Asp141Tyr) c.361G>T (p.Asp121Tyr) | gnomAD v4 |
| 18 | g.62360005A>C | CA402613696 | TNFRSF11A | c.572A>C (p.Asp191Ala) n.490A>C c.530A>C (p.Asp177Ala) c.587A>C (p.Asp196Ala) c.464A>C (p.Asp155Ala) n.602A>C c.422A>C (p.Asp141Ala) c.362A>C (p.Asp121Ala) | |
| 18 | g.62360005A>G | CA402613695 | TNFRSF11A | c.572A>G (p.Asp191Gly) n.490A>G c.530A>G (p.Asp177Gly) c.587A>G (p.Asp196Gly) c.464A>G (p.Asp155Gly) n.602A>G c.422A>G (p.Asp141Gly) c.362A>G (p.Asp121Gly) | |
| 18 | g.62360005A>T | CA402613693 | TNFRSF11A | c.572A>T (p.Asp191Val) n.490A>T c.530A>T (p.Asp177Val) c.587A>T (p.Asp196Val) c.464A>T (p.Asp155Val) n.602A>T c.422A>T (p.Asp141Val) c.362A>T (p.Asp121Val) | |
| 18 | g.62360006T>A | CA402613697 | TNFRSF11A | c.573T>A (p.Asp191Glu) n.491T>A c.531T>A (p.Asp177Glu) c.588T>A (p.Asp196Glu) c.465T>A (p.Asp155Glu) n.603T>A c.423T>A (p.Asp141Glu) c.363T>A (p.Asp121Glu) | |
| 18 | g.62360006T>C | CA301697956 | TNFRSF11A | c.573T>C (p.Asp191=) n.491T>C c.531T>C (p.Asp177=) c.588T>C (p.Asp196=) c.465T>C (p.Asp155=) n.603T>C c.423T>C (p.Asp141=) c.363T>C (p.Asp121=) | ClinVar dbSNP gnomAD v4 |
| 18 | g.62360006T>G | CA402613698 | TNFRSF11A | c.573T>G (p.Asp191Glu) n.491T>G c.531T>G (p.Asp177Glu) c.588T>G (p.Asp196Glu) c.465T>G (p.Asp155Glu) n.603T>G c.423T>G (p.Asp141Glu) c.363T>G (p.Asp121Glu) | |
| 18 | g.62360006T= | CA2308285232 | TNFRSF11A | c.573T= (p.Asp191=) n.491T= c.531T= (p.Asp177=) c.588T= (p.Asp196=) c.465T= (p.Asp155=) n.603T= c.423T= (p.Asp141=) c.363T= (p.Asp121=) | |
| 18 | g.62360007G>A | CA301697960 | TNFRSF11A | c.574G>A (p.Ala192Thr) n.492G>A c.532G>A (p.Ala178Thr) c.589G>A (p.Ala197Thr) c.466G>A (p.Ala156Thr) n.604G>A c.424G>A (p.Ala142Thr) c.364G>A (p.Ala122Thr) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 18 | g.62360007G>C | CA402613704 | TNFRSF11A | c.574G>C (p.Ala192Pro) n.492G>C c.532G>C (p.Ala178Pro) c.589G>C (p.Ala197Pro) c.466G>C (p.Ala156Pro) n.604G>C c.424G>C (p.Ala142Pro) c.364G>C (p.Ala122Pro) | |
| 18 | g.62360007G= | CA2308285233 | TNFRSF11A | c.574G= (p.Ala192=) n.492G= c.532G= (p.Ala178=) c.589G= (p.Ala197=) c.466G= (p.Ala156=) n.604G= c.424G= (p.Ala142=) c.364G= (p.Ala122=) | |
| 18 | g.62360007G>T | CA402613702 | TNFRSF11A | c.574G>T (p.Ala192Ser) n.492G>T c.532G>T (p.Ala178Ser) c.589G>T (p.Ala197Ser) c.466G>T (p.Ala156Ser) n.604G>T c.424G>T (p.Ala142Ser) c.364G>T (p.Ala122Ser) | |
| 18 | g.62360008C>A | CA402613705 | TNFRSF11A | c.575C>A (p.Ala192Glu) n.493C>A c.533C>A (p.Ala178Glu) c.590C>A (p.Ala197Glu) c.467C>A (p.Ala156Glu) n.605C>A c.425C>A (p.Ala142Glu) c.365C>A (p.Ala122Glu) | dbSNP |
| 18 | g.62360008C= | CA2308285234 | TNFRSF11A | c.575C= (p.Ala192=) n.493C= c.533C= (p.Ala178=) c.590C= (p.Ala197=) c.467C= (p.Ala156=) n.605C= c.425C= (p.Ala142=) c.365C= (p.Ala122=) | |
| 18 | g.62360008C>G | CA402613707 | TNFRSF11A | c.575C>G (p.Ala192Gly) n.493C>G c.533C>G (p.Ala178Gly) c.590C>G (p.Ala197Gly) c.467C>G (p.Ala156Gly) n.605C>G c.425C>G (p.Ala142Gly) c.365C>G (p.Ala122Gly) | gnomAD v3 gnomAD v4 |
| 18 | g.62360008C>T | CA8983802 | TNFRSF11A | c.575C>T (p.Ala192Val) n.493C>T c.533C>T (p.Ala178Val) c.590C>T (p.Ala197Val) c.467C>T (p.Ala156Val) n.605C>T c.425C>T (p.Ala142Val) c.365C>T (p.Ala122Val) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 18 | g.62360009G>A | CA8983803 | TNFRSF11A | c.576G>A (p.Ala192=) n.494G>A c.534G>A (p.Ala178=) c.591G>A (p.Ala197=) c.468G>A (p.Ala156=) n.606G>A c.426G>A (p.Ala142=) c.366G>A (p.Ala122=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 18 | g.62360009G>C | CA504079071 | TNFRSF11A | c.576G>C (p.Ala192=) n.494G>C c.534G>C (p.Ala178=) c.591G>C (p.Ala197=) c.468G>C (p.Ala156=) n.606G>C c.426G>C (p.Ala142=) c.366G>C (p.Ala122=) | |
| 18 | g.62360009G= | CA2308285235 | TNFRSF11A | c.576G= (p.Ala192=) n.494G= c.534G= (p.Ala178=) c.591G= (p.Ala197=) c.468G= (p.Ala156=) n.606G= c.426G= (p.Ala142=) c.366G= (p.Ala122=) | |
| 18 | g.62360009G>T | CA504079073 | TNFRSF11A | c.576G>T (p.Ala192=) n.494G>T c.534G>T (p.Ala178=) c.591G>T (p.Ala197=) c.468G>T (p.Ala156=) n.606G>T c.426G>T (p.Ala142=) c.366G>T (p.Ala122=) | |
| 18 | g.62360010G>A | CA402613710 | TNFRSF11A | c.577G>A (p.Val193Ile) n.495G>A c.535G>A (p.Val179Ile) c.592G>A (p.Val198Ile) c.469G>A (p.Val157Ile) n.607G>A c.427G>A (p.Val143Ile) c.367G>A (p.Val123Ile) | dbSNP gnomAD v2 gnomAD v4 |
| 18 | g.62360010G>C | CA402613712 | TNFRSF11A | c.577G>C (p.Val193Leu) n.495G>C c.535G>C (p.Val179Leu) c.592G>C (p.Val198Leu) c.469G>C (p.Val157Leu) n.607G>C c.427G>C (p.Val143Leu) c.367G>C (p.Val123Leu) | |
| 18 | g.62360010G= | CA2308285236 | TNFRSF11A | c.577G= (p.Val193=) n.495G= c.535G= (p.Val179=) c.592G= (p.Val198=) c.469G= (p.Val157=) n.607G= c.427G= (p.Val143=) c.367G= (p.Val123=) | |
| 18 | g.62360010G>T | CA402613713 | TNFRSF11A | c.577G>T (p.Val193Phe) n.495G>T c.535G>T (p.Val179Phe) c.592G>T (p.Val198Phe) c.469G>T (p.Val157Phe) n.607G>T c.427G>T (p.Val143Phe) c.367G>T (p.Val123Phe) | COSMIC |
| 18 | g.62360011T>A | CA402613716 | TNFRSF11A | c.578T>A (p.Val193Asp) n.496T>A c.536T>A (p.Val179Asp) c.593T>A (p.Val198Asp) c.470T>A (p.Val157Asp) n.608T>A c.428T>A (p.Val143Asp) c.368T>A (p.Val123Asp) | |
| 18 | g.62360011T>C | CA402613717 | TNFRSF11A | c.578T>C (p.Val193Ala) n.496T>C c.536T>C (p.Val179Ala) c.593T>C (p.Val198Ala) c.470T>C (p.Val157Ala) n.608T>C c.428T>C (p.Val143Ala) c.368T>C (p.Val123Ala) | |
| 18 | g.62360011T>G | CA402613719 | TNFRSF11A | c.578T>G (p.Val193Gly) n.496T>G c.536T>G (p.Val179Gly) c.593T>G (p.Val198Gly) c.470T>G (p.Val157Gly) n.608T>G c.428T>G (p.Val143Gly) c.368T>G (p.Val123Gly) | |
| 18 | g.62360012T>A | CA504079082 | TNFRSF11A | c.579T>A (p.Val193=) n.497T>A c.537T>A (p.Val179=) c.594T>A (p.Val198=) c.471T>A (p.Val157=) n.609T>A c.429T>A (p.Val143=) c.369T>A (p.Val123=) | |
| 18 | g.62360012T>C | CA504079083 | TNFRSF11A | c.579T>C (p.Val193=) n.497T>C c.537T>C (p.Val179=) c.594T>C (p.Val198=) c.471T>C (p.Val157=) n.609T>C c.429T>C (p.Val143=) c.369T>C (p.Val123=) | gnomAD v4 |
| 18 | g.62360012T>G | CA504079084 | TNFRSF11A | c.579T>G (p.Val193=) n.497T>G c.537T>G (p.Val179=) c.594T>G (p.Val198=) c.471T>G (p.Val157=) n.609T>G c.429T>G (p.Val143=) c.369T>G (p.Val123=) | gnomAD v4 |
| 18 | g.62360013T>A | CA402613720 | TNFRSF11A | c.580T>A (p.Cys194Ser) n.498T>A c.538T>A (p.Cys180Ser) c.595T>A (p.Cys199Ser) c.472T>A (p.Cys158Ser) n.610T>A c.430T>A (p.Cys144Ser) c.370T>A (p.Cys124Ser) | |
| 18 | g.62360013T>C | CA402613722 | TNFRSF11A | c.580T>C (p.Cys194Arg) n.498T>C c.538T>C (p.Cys180Arg) c.595T>C (p.Cys199Arg) c.472T>C (p.Cys158Arg) n.610T>C c.430T>C (p.Cys144Arg) c.370T>C (p.Cys124Arg) | |
| 18 | g.62360013T>G | CA402613724 | TNFRSF11A | c.580T>G (p.Cys194Gly) n.498T>G c.538T>G (p.Cys180Gly) c.595T>G (p.Cys199Gly) c.472T>G (p.Cys158Gly) n.610T>G c.430T>G (p.Cys144Gly) c.370T>G (p.Cys124Gly) | |
| 18 | g.62360014G>A | CA402613726 | TNFRSF11A | c.581G>A (p.Cys194Tyr) n.499G>A c.539G>A (p.Cys180Tyr) c.596G>A (p.Cys199Tyr) c.473G>A (p.Cys158Tyr) n.611G>A c.431G>A (p.Cys144Tyr) c.371G>A (p.Cys124Tyr) | |
| 18 | g.62360014G>C | CA402613728 | TNFRSF11A | c.581G>C (p.Cys194Ser) n.499G>C c.539G>C (p.Cys180Ser) c.596G>C (p.Cys199Ser) c.473G>C (p.Cys158Ser) n.611G>C c.431G>C (p.Cys144Ser) c.371G>C (p.Cys124Ser) | |
| 18 | g.62360014G>T | CA402613729 | TNFRSF11A | c.581G>T (p.Cys194Phe) n.499G>T c.539G>T (p.Cys180Phe) c.596G>T (p.Cys199Phe) c.473G>T (p.Cys158Phe) n.611G>T c.431G>T (p.Cys144Phe) c.371G>T (p.Cys124Phe) | |
| 18 | g.62360015C>A | CA402613731 | TNFRSF11A | c.582C>A (p.Cys194Ter) n.500C>A c.540C>A (p.Cys180Ter) c.597C>A (p.Cys199Ter) c.474C>A (p.Cys158Ter) n.612C>A c.432C>A (p.Cys144Ter) c.372C>A (p.Cys124Ter) | |
| 18 | g.62360015C= | CA2308285237 | TNFRSF11A | c.582C= (p.Cys194=) n.500C= c.540C= (p.Cys180=) c.597C= (p.Cys199=) c.474C= (p.Cys158=) n.612C= c.432C= (p.Cys144=) c.372C= (p.Cys124=) | |
| 18 | g.62360015C>G | CA402613732 | TNFRSF11A | c.582C>G (p.Cys194Trp) n.500C>G c.540C>G (p.Cys180Trp) c.597C>G (p.Cys199Trp) c.474C>G (p.Cys158Trp) n.612C>G c.432C>G (p.Cys144Trp) c.372C>G (p.Cys124Trp) | |
| 18 | g.62360015C>T | CA504079095 | TNFRSF11A | c.582C>T (p.Cys194=) n.500C>T c.540C>T (p.Cys180=) c.597C>T (p.Cys199=) c.474C>T (p.Cys158=) n.612C>T c.432C>T (p.Cys144=) c.372C>T (p.Cys124=) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 18 | g.62360016A>C | CA402613734 | TNFRSF11A | c.583A>C (p.Ser195Arg) n.501A>C c.541A>C (p.Ser181Arg) c.598A>C (p.Ser200Arg) c.475A>C (p.Ser159Arg) n.613A>C c.433A>C (p.Ser145Arg) c.373A>C (p.Ser125Arg) | |
| 18 | g.62360016A>G | CA402613736 | TNFRSF11A | c.583A>G (p.Ser195Gly) n.501A>G c.541A>G (p.Ser181Gly) c.598A>G (p.Ser200Gly) c.475A>G (p.Ser159Gly) n.613A>G c.433A>G (p.Ser145Gly) c.373A>G (p.Ser125Gly) | |
| 18 | g.62360016A>T | CA402613738 | TNFRSF11A | c.583A>T (p.Ser195Cys) n.501A>T c.541A>T (p.Ser181Cys) c.598A>T (p.Ser200Cys) c.475A>T (p.Ser159Cys) n.613A>T c.433A>T (p.Ser145Cys) c.373A>T (p.Ser125Cys) | |
| 18 | g.62360017G>A | CA402613740 | TNFRSF11A | c.584G>A (p.Ser195Asn) n.502G>A c.542G>A (p.Ser181Asn) c.599G>A (p.Ser200Asn) c.476G>A (p.Ser159Asn) n.614G>A c.434G>A (p.Ser145Asn) c.374G>A (p.Ser125Asn) | COSMIC |
| 18 | g.62360017G>C | CA402613741 | TNFRSF11A | c.584G>C (p.Ser195Thr) n.502G>C c.542G>C (p.Ser181Thr) c.599G>C (p.Ser200Thr) c.476G>C (p.Ser159Thr) n.614G>C c.434G>C (p.Ser145Thr) c.374G>C (p.Ser125Thr) | gnomAD v4 |
| 18 | g.62360017G>T | CA402613743 | TNFRSF11A | c.584G>T (p.Ser195Ile) n.502G>T c.542G>T (p.Ser181Ile) c.599G>T (p.Ser200Ile) c.476G>T (p.Ser159Ile) n.614G>T c.434G>T (p.Ser145Ile) c.374G>T (p.Ser125Ile) | |
| 18 | g.62360018T>A | CA402613744 | TNFRSF11A | c.585T>A (p.Ser195Arg) n.503T>A c.543T>A (p.Ser181Arg) c.600T>A (p.Ser200Arg) c.477T>A (p.Ser159Arg) n.615T>A c.435T>A (p.Ser145Arg) c.375T>A (p.Ser125Arg) | |
| 18 | g.62360018T>C | CA504079102 | TNFRSF11A | c.585T>C (p.Ser195=) n.503T>C c.543T>C (p.Ser181=) c.600T>C (p.Ser200=) c.477T>C (p.Ser159=) n.615T>C c.435T>C (p.Ser145=) c.375T>C (p.Ser125=) | |
| 18 | g.62360018T>G | CA402613745 | TNFRSF11A | c.585T>G (p.Ser195Arg) n.503T>G c.543T>G (p.Ser181Arg) c.600T>G (p.Ser200Arg) c.477T>G (p.Ser159Arg) n.615T>G c.435T>G (p.Ser145Arg) c.375T>G (p.Ser125Arg) | |
| 18 | g.62360019T>A | CA402613747 | TNFRSF11A | c.586T>A (p.Ser196Thr) n.504T>A c.544T>A (p.Ser182Thr) c.601T>A (p.Ser201Thr) c.478T>A (p.Ser160Thr) n.616T>A c.436T>A (p.Ser146Thr) c.376T>A (p.Ser126Thr) | |
| 18 | g.62360019T>C | CA402613749 | TNFRSF11A | c.586T>C (p.Ser196Pro) n.504T>C c.544T>C (p.Ser182Pro) c.601T>C (p.Ser201Pro) c.478T>C (p.Ser160Pro) n.616T>C c.436T>C (p.Ser146Pro) c.376T>C (p.Ser126Pro) | |
| 18 | g.62360019T>G | CA402613751 | TNFRSF11A | c.586T>G (p.Ser196Ala) n.504T>G c.544T>G (p.Ser182Ala) c.601T>G (p.Ser201Ala) c.478T>G (p.Ser160Ala) n.616T>G c.436T>G (p.Ser146Ala) c.376T>G (p.Ser126Ala) | |
| 18 | g.62360020C>A | CA402613756 | TNFRSF11A | c.587C>A (p.Ser196Tyr) n.505C>A c.545C>A (p.Ser182Tyr) c.602C>A (p.Ser201Tyr) c.479C>A (p.Ser160Tyr) n.617C>A c.437C>A (p.Ser146Tyr) c.377C>A (p.Ser126Tyr) | |
| 18 | g.62360020C>G | CA402613754 | TNFRSF11A | c.587C>G (p.Ser196Cys) n.505C>G c.545C>G (p.Ser182Cys) c.602C>G (p.Ser201Cys) c.479C>G (p.Ser160Cys) n.617C>G c.437C>G (p.Ser146Cys) c.377C>G (p.Ser126Cys) | |
| 18 | g.62360020C>T | CA402613752 | TNFRSF11A | c.587C>T (p.Ser196Phe) n.505C>T c.545C>T (p.Ser182Phe) c.602C>T (p.Ser201Phe) c.479C>T (p.Ser160Phe) n.617C>T c.437C>T (p.Ser146Phe) c.377C>T (p.Ser126Phe) | |
| 18 | g.62360021T>A | CA504079114 | TNFRSF11A | c.588T>A (p.Ser196=) n.506T>A c.546T>A (p.Ser182=) c.603T>A (p.Ser201=) c.480T>A (p.Ser160=) n.618T>A c.438T>A (p.Ser146=) c.378T>A (p.Ser126=) | |
| 18 | g.62360021T>C | CA504079115 | TNFRSF11A | c.588T>C (p.Ser196=) n.506T>C c.546T>C (p.Ser182=) c.603T>C (p.Ser201=) c.480T>C (p.Ser160=) n.618T>C c.438T>C (p.Ser146=) c.378T>C (p.Ser126=) | |
| 18 | g.62360021T>G | CA504079118 | TNFRSF11A | c.588T>G (p.Ser196=) n.506T>G c.546T>G (p.Ser182=) c.603T>G (p.Ser201=) c.480T>G (p.Ser160=) n.618T>G c.438T>G (p.Ser146=) c.378T>G (p.Ser126=) | |
| 18 | g.62360022T>A | CA402613760 | TNFRSF11A | c.589T>A (p.Ser197Thr) n.507T>A c.547T>A (p.Ser183Thr) c.604T>A (p.Ser202Thr) c.481T>A (p.Ser161Thr) n.619T>A c.439T>A (p.Ser147Thr) c.379T>A (p.Ser127Thr) | |
| 18 | g.62360022T>C | CA402613758 | TNFRSF11A | c.589T>C (p.Ser197Pro) n.507T>C c.547T>C (p.Ser183Pro) c.604T>C (p.Ser202Pro) c.481T>C (p.Ser161Pro) n.619T>C c.439T>C (p.Ser147Pro) c.379T>C (p.Ser127Pro) | |
| 18 | g.62360022T>G | CA402613759 | TNFRSF11A | c.589T>G (p.Ser197Ala) n.507T>G c.547T>G (p.Ser183Ala) c.604T>G (p.Ser202Ala) c.481T>G (p.Ser161Ala) n.619T>G c.439T>G (p.Ser147Ala) c.379T>G (p.Ser127Ala) | |
| 18 | g.62360023C>A | CA402613762 | TNFRSF11A | c.590C>A (p.Ser197Tyr) n.508C>A c.548C>A (p.Ser183Tyr) c.605C>A (p.Ser202Tyr) c.482C>A (p.Ser161Tyr) n.620C>A c.440C>A (p.Ser147Tyr) c.380C>A (p.Ser127Tyr) | |
| 18 | g.62360023C>G | CA402613764 | TNFRSF11A | c.590C>G (p.Ser197Cys) n.508C>G c.548C>G (p.Ser183Cys) c.605C>G (p.Ser202Cys) c.482C>G (p.Ser161Cys) n.620C>G c.440C>G (p.Ser147Cys) c.380C>G (p.Ser127Cys) | |
| 18 | g.62360023C>T | CA402613766 | TNFRSF11A | c.590C>T (p.Ser197Phe) n.508C>T c.548C>T (p.Ser183Phe) c.605C>T (p.Ser202Phe) c.482C>T (p.Ser161Phe) n.620C>T c.440C>T (p.Ser147Phe) c.380C>T (p.Ser127Phe) | gnomAD v4 |
| 18 | g.62360024T>A | CA504079128 | TNFRSF11A | c.591T>A (p.Ser197=) n.509T>A c.549T>A (p.Ser183=) c.606T>A (p.Ser202=) c.483T>A (p.Ser161=) n.621T>A c.441T>A (p.Ser147=) c.381T>A (p.Ser127=) | |
| 18 | g.62360024T>C | CA504079132 | TNFRSF11A | c.591T>C (p.Ser197=) n.509T>C c.549T>C (p.Ser183=) c.606T>C (p.Ser202=) c.483T>C (p.Ser161=) n.621T>C c.441T>C (p.Ser147=) c.381T>C (p.Ser127=) | |
| 18 | g.62360024T>G | CA504079130 | TNFRSF11A | c.591T>G (p.Ser197=) n.509T>G c.549T>G (p.Ser183=) c.606T>G (p.Ser202=) c.483T>G (p.Ser161=) n.621T>G c.441T>G (p.Ser147=) c.381T>G (p.Ser127=) | |
| 18 | g.62360025C>A | CA402613768 | TNFRSF11A | c.592C>A (p.Leu198Met) n.510C>A c.550C>A (p.Leu184Met) c.607C>A (p.Leu203Met) c.484C>A (p.Leu162Met) n.622C>A c.442C>A (p.Leu148Met) c.382C>A (p.Leu128Met) | |
| 18 | g.62360025C>G | CA402613770 | TNFRSF11A | c.592C>G (p.Leu198Val) n.510C>G c.550C>G (p.Leu184Val) c.607C>G (p.Leu203Val) c.484C>G (p.Leu162Val) n.622C>G c.442C>G (p.Leu148Val) c.382C>G (p.Leu128Val) | |
| 18 | g.62360025C>T | CA504079136 | TNFRSF11A | c.592C>T (p.Leu198=) n.510C>T c.550C>T (p.Leu184=) c.607C>T (p.Leu203=) c.484C>T (p.Leu162=) n.622C>T c.442C>T (p.Leu148=) c.382C>T (p.Leu128=) | |
| 18 | g.62360026T>A | CA402613772 | TNFRSF11A | c.593T>A (p.Leu198Gln) n.511T>A c.551T>A (p.Leu184Gln) c.608T>A (p.Leu203Gln) c.485T>A (p.Leu162Gln) n.623T>A c.443T>A (p.Leu148Gln) c.383T>A (p.Leu128Gln) | |
| 18 | g.62360026T>C | CA402613773 | TNFRSF11A | c.593T>C (p.Leu198Pro) n.511T>C c.551T>C (p.Leu184Pro) c.608T>C (p.Leu203Pro) c.485T>C (p.Leu162Pro) n.623T>C c.443T>C (p.Leu148Pro) c.383T>C (p.Leu128Pro) | gnomAD v4 |
| 18 | g.62360026T>G | CA402613774 | TNFRSF11A | c.593T>G (p.Leu198Arg) n.511T>G c.551T>G (p.Leu184Arg) c.608T>G (p.Leu203Arg) c.485T>G (p.Leu162Arg) n.623T>G c.443T>G (p.Leu148Arg) c.383T>G (p.Leu128Arg) | |
| 18 | g.62360027G>A | CA504079143 | TNFRSF11A | c.594G>A (p.Leu198=) n.512G>A c.552G>A (p.Leu184=) c.609G>A (p.Leu203=) c.486G>A (p.Leu162=) n.624G>A c.444G>A (p.Leu148=) c.384G>A (p.Leu128=) | ClinVar |
| 18 | g.62360027G>C | CA504079145 | TNFRSF11A | c.594G>C (p.Leu198=) n.512G>C c.552G>C (p.Leu184=) c.609G>C (p.Leu203=) c.486G>C (p.Leu162=) n.624G>C c.444G>C (p.Leu148=) c.384G>C (p.Leu128=) | |
| 18 | g.62360027G>T | CA504079147 | TNFRSF11A | c.594G>T (p.Leu198=) n.512G>T c.552G>T (p.Leu184=) c.609G>T (p.Leu203=) c.486G>T (p.Leu162=) n.624G>T c.444G>T (p.Leu148=) c.384G>T (p.Leu128=) | |
| 18 | g.62360028C>A | CA402613777 | TNFRSF11A | c.595C>A (p.Pro199Thr) n.513C>A c.553C>A (p.Pro185Thr) c.610C>A (p.Pro204Thr) c.487C>A (p.Pro163Thr) n.625C>A c.445C>A (p.Pro149Thr) c.385C>A (p.Pro129Thr) | |
| 18 | g.62360028C>G | CA402613779 | TNFRSF11A | c.595C>G (p.Pro199Ala) n.513C>G c.553C>G (p.Pro185Ala) c.610C>G (p.Pro204Ala) c.487C>G (p.Pro163Ala) n.625C>G c.445C>G (p.Pro149Ala) c.385C>G (p.Pro129Ala) | |
| 18 | g.62360028C>T | CA402613780 | TNFRSF11A | c.595C>T (p.Pro199Ser) n.513C>T c.553C>T (p.Pro185Ser) c.610C>T (p.Pro204Ser) c.487C>T (p.Pro163Ser) n.625C>T c.445C>T (p.Pro149Ser) c.385C>T (p.Pro129Ser) | |
| 18 | g.62360029C>A | CA402613786 | TNFRSF11A | c.596C>A (p.Pro199Gln) n.514C>A c.554C>A (p.Pro185Gln) c.611C>A (p.Pro204Gln) c.488C>A (p.Pro163Gln) n.626C>A c.446C>A (p.Pro149Gln) c.386C>A (p.Pro129Gln) | |
| 18 | g.62360029C>G | CA402613782 | TNFRSF11A | c.596C>G (p.Pro199Arg) n.514C>G c.554C>G (p.Pro185Arg) c.611C>G (p.Pro204Arg) c.488C>G (p.Pro163Arg) n.626C>G c.446C>G (p.Pro149Arg) c.386C>G (p.Pro129Arg) | |
| 18 | g.62360029C>T | CA402613784 | TNFRSF11A | c.596C>T (p.Pro199Leu) n.514C>T c.554C>T (p.Pro185Leu) c.611C>T (p.Pro204Leu) c.488C>T (p.Pro163Leu) n.626C>T c.446C>T (p.Pro149Leu) c.386C>T (p.Pro129Leu) | |
| 18 | g.62360030A= | CA2308285238 | TNFRSF11A | c.597A= (p.Pro199=) n.515A= c.555A= (p.Pro185=) c.612A= (p.Pro204=) c.489A= (p.Pro163=) n.627A= c.447A= (p.Pro149=) c.387A= (p.Pro129=) | |
| 18 | g.62360030A>C | CA504079156 | TNFRSF11A | c.597A>C (p.Pro199=) n.515A>C c.555A>C (p.Pro185=) c.612A>C (p.Pro204=) c.489A>C (p.Pro163=) n.627A>C c.447A>C (p.Pro149=) c.387A>C (p.Pro129=) | |
| 18 | g.62360030A>G | CA504079160 | TNFRSF11A | c.597A>G (p.Pro199=) n.515A>G c.555A>G (p.Pro185=) c.612A>G (p.Pro204=) c.489A>G (p.Pro163=) n.627A>G c.447A>G (p.Pro149=) c.387A>G (p.Pro129=) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 18 | g.62360030A>T | CA504079163 | TNFRSF11A | c.597A>T (p.Pro199=) n.515A>T c.555A>T (p.Pro185=) c.612A>T (p.Pro204=) c.489A>T (p.Pro163=) n.627A>T c.447A>T (p.Pro149=) c.387A>T (p.Pro129=) | |
| 18 | g.62360031G>A | CA402613787 | TNFRSF11A | c.598G>A (p.Ala200Thr) n.516G>A c.556G>A (p.Ala186Thr) c.613G>A (p.Ala205Thr) c.490G>A (p.Ala164Thr) n.628G>A c.448G>A (p.Ala150Thr) c.388G>A (p.Ala130Thr) | ClinVar gnomAD v4 |
| 18 | g.62360031G>C | CA402613789 | TNFRSF11A | c.598G>C (p.Ala200Pro) n.516G>C c.556G>C (p.Ala186Pro) c.613G>C (p.Ala205Pro) c.490G>C (p.Ala164Pro) n.628G>C c.448G>C (p.Ala150Pro) c.388G>C (p.Ala130Pro) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 18 | g.62360031G= | CA2308285239 | TNFRSF11A | c.598G= (p.Ala200=) n.516G= c.556G= (p.Ala186=) c.613G= (p.Ala205=) c.490G= (p.Ala164=) n.628G= c.448G= (p.Ala150=) c.388G= (p.Ala130=) | |
| 18 | g.62360031G>T | CA402613791 | TNFRSF11A | c.598G>T (p.Ala200Ser) n.516G>T c.556G>T (p.Ala186Ser) c.613G>T (p.Ala205Ser) c.490G>T (p.Ala164Ser) n.628G>T c.448G>T (p.Ala150Ser) c.388G>T (p.Ala130Ser) | |
| 18 | g.62360032C>A | CA402613793 | TNFRSF11A | c.599C>A (p.Ala200Asp) n.517C>A c.557C>A (p.Ala186Asp) c.614C>A (p.Ala205Asp) c.491C>A (p.Ala164Asp) n.629C>A c.449C>A (p.Ala150Asp) c.389C>A (p.Ala130Asp) | |
| 18 | g.62360032C>G | CA402613794 | TNFRSF11A | c.599C>G (p.Ala200Gly) n.517C>G c.557C>G (p.Ala186Gly) c.614C>G (p.Ala205Gly) c.491C>G (p.Ala164Gly) n.629C>G c.449C>G (p.Ala150Gly) c.389C>G (p.Ala130Gly) | |
| 18 | g.62360032C>T | CA402613795 | TNFRSF11A | c.599C>T (p.Ala200Val) n.517C>T c.557C>T (p.Ala186Val) c.614C>T (p.Ala205Val) c.491C>T (p.Ala164Val) n.629C>T c.449C>T (p.Ala150Val) c.389C>T (p.Ala130Val) | |
| 18 | g.62360033T>A | CA504079175 | TNFRSF11A | c.600T>A (p.Ala200=) n.518T>A c.558T>A (p.Ala186=) c.615T>A (p.Ala205=) c.492T>A (p.Ala164=) n.630T>A c.450T>A (p.Ala150=) c.390T>A (p.Ala130=) | |
| 18 | g.62360033T>C | CA504079177 | TNFRSF11A | c.600T>C (p.Ala200=) n.518T>C c.558T>C (p.Ala186=) c.615T>C (p.Ala205=) c.492T>C (p.Ala164=) n.630T>C c.450T>C (p.Ala150=) c.390T>C (p.Ala130=) | gnomAD v4 |
| 18 | g.62360033T>G | CA504079178 | TNFRSF11A | c.600T>G (p.Ala200=) n.518T>G c.558T>G (p.Ala186=) c.615T>G (p.Ala205=) c.492T>G (p.Ala164=) n.630T>G c.450T>G (p.Ala150=) c.390T>G (p.Ala130=) | |
| 18 | g.62360034A= | CA2308285240 | TNFRSF11A | c.601A= (p.Arg201=) n.519A= c.559A= (p.Arg187=) c.616A= (p.Arg206=) c.493A= (p.Arg165=) n.631A= c.451A= (p.Arg151=) c.391A= (p.Arg131=) | |
| 18 | g.62360034A>C | CA504079179 | TNFRSF11A | c.601A>C (p.Arg201=) n.519A>C c.559A>C (p.Arg187=) c.616A>C (p.Arg206=) c.493A>C (p.Arg165=) n.631A>C c.451A>C (p.Arg151=) c.391A>C (p.Arg131=) | |
| 18 | g.62360034A>G | CA402613797 | TNFRSF11A | c.601A>G (p.Arg201Gly) n.519A>G c.559A>G (p.Arg187Gly) c.616A>G (p.Arg206Gly) c.493A>G (p.Arg165Gly) n.631A>G c.451A>G (p.Arg151Gly) c.391A>G (p.Arg131Gly) | dbSNP gnomAD v4 |
| 18 | g.62360034A>T | CA402613799 | TNFRSF11A | c.601A>T (p.Arg201Ter) n.519A>T c.559A>T (p.Arg187Ter) c.616A>T (p.Arg206Ter) c.493A>T (p.Arg165Ter) n.631A>T c.451A>T (p.Arg151Ter) c.391A>T (p.Arg131Ter) | |
| 18 | g.62360035G>A | CA402613801 | TNFRSF11A | c.602G>A (p.Arg201Lys) n.520G>A c.560G>A (p.Arg187Lys) c.617G>A (p.Arg206Lys) c.494G>A (p.Arg165Lys) n.632G>A c.452G>A (p.Arg151Lys) c.392G>A (p.Arg131Lys) | |
| 18 | g.62360035G>C | CA402613803 | TNFRSF11A | c.602G>C (p.Arg201Thr) n.520G>C c.560G>C (p.Arg187Thr) c.617G>C (p.Arg206Thr) c.494G>C (p.Arg165Thr) n.632G>C c.452G>C (p.Arg151Thr) c.392G>C (p.Arg131Thr) | gnomAD v4 |
| 18 | g.62360035G>T | CA402613804 | TNFRSF11A | c.602G>T (p.Arg201Ile) n.520G>T c.560G>T (p.Arg187Ile) c.617G>T (p.Arg206Ile) c.494G>T (p.Arg165Ile) n.632G>T c.452G>T (p.Arg151Ile) c.392G>T (p.Arg131Ile) | |
| 18 | g.62360036A>C | CA402613806 | TNFRSF11A | c.603A>C (p.Arg201Ser) n.521A>C c.561A>C (p.Arg187Ser) c.618A>C (p.Arg206Ser) c.495A>C (p.Arg165Ser) n.633A>C c.453A>C (p.Arg151Ser) c.393A>C (p.Arg131Ser) | |
| 18 | g.62360036A>G | CA504079195 | TNFRSF11A | c.603A>G (p.Arg201=) n.521A>G c.561A>G (p.Arg187=) c.618A>G (p.Arg206=) c.495A>G (p.Arg165=) n.633A>G c.453A>G (p.Arg151=) c.393A>G (p.Arg131=) | gnomAD v4 |
| 18 | g.62360036A>T | CA402613808 | TNFRSF11A | c.603A>T (p.Arg201Ser) n.521A>T c.561A>T (p.Arg187Ser) c.618A>T (p.Arg206Ser) c.495A>T (p.Arg165Ser) n.633A>T c.453A>T (p.Arg151Ser) c.393A>T (p.Arg131Ser) | |
| 18 | g.62360039dup | CA2642068405 | TNFRSF11A | c.606dup (p.Pro203ThrfsTer4) c.606dup (p.Pro203ThrfsTer11) n.524dup c.564dup (p.Pro189ThrfsTer4) c.621dup (p.Pro208ThrfsTer4) c.498dup (p.Pro167ThrfsTer4) n.636dup c.456dup (p.Pro153ThrfsTer4) c.396dup (p.Pro133ThrfsTer4) | gnomAD v4 |
| 18 | g.62360037A>C | CA402613812 | TNFRSF11A | c.604A>C (p.Lys202Gln) n.522A>C c.562A>C (p.Lys188Gln) c.619A>C (p.Lys207Gln) c.496A>C (p.Lys166Gln) n.634A>C c.454A>C (p.Lys152Gln) c.394A>C (p.Lys132Gln) | |
| 18 | g.62360037A>G | CA402613813 | TNFRSF11A | c.604A>G (p.Lys202Glu) n.522A>G c.562A>G (p.Lys188Glu) c.619A>G (p.Lys207Glu) c.496A>G (p.Lys166Glu) n.634A>G c.454A>G (p.Lys152Glu) c.394A>G (p.Lys132Glu) | |
| 18 | g.62360037A>T | CA402613810 | TNFRSF11A | c.604A>T (p.Lys202Ter) n.522A>T c.562A>T (p.Lys188Ter) c.619A>T (p.Lys207Ter) c.496A>T (p.Lys166Ter) n.634A>T c.454A>T (p.Lys152Ter) c.394A>T (p.Lys132Ter) | |
| 18 | g.62360038A>C | CA402613816 | TNFRSF11A | c.605A>C (p.Lys202Thr) n.523A>C c.563A>C (p.Lys188Thr) c.620A>C (p.Lys207Thr) c.497A>C (p.Lys166Thr) n.635A>C c.455A>C (p.Lys152Thr) c.395A>C (p.Lys132Thr) | |
| 18 | g.62360038A>G | CA402613818 | TNFRSF11A | c.605A>G (p.Lys202Arg) n.523A>G c.563A>G (p.Lys188Arg) c.620A>G (p.Lys207Arg) c.497A>G (p.Lys166Arg) n.635A>G c.455A>G (p.Lys152Arg) c.395A>G (p.Lys132Arg) | |
| 18 | g.62360038A>T | CA402613817 | TNFRSF11A | c.605A>T (p.Lys202Ile) n.523A>T c.563A>T (p.Lys188Ile) c.620A>T (p.Lys207Ile) c.497A>T (p.Lys166Ile) n.635A>T c.455A>T (p.Lys152Ile) c.395A>T (p.Lys132Ile) | |
| 18 | g.62360039A>C | CA402613820 | TNFRSF11A | c.606A>C (p.Lys202Asn) n.524A>C c.564A>C (p.Lys188Asn) c.621A>C (p.Lys207Asn) c.498A>C (p.Lys166Asn) n.636A>C c.456A>C (p.Lys152Asn) c.396A>C (p.Lys132Asn) | |
| 18 | g.62360039A>G | CA504079204 | TNFRSF11A | c.606A>G (p.Lys202=) n.524A>G c.564A>G (p.Lys188=) c.621A>G (p.Lys207=) c.498A>G (p.Lys166=) n.636A>G c.456A>G (p.Lys152=) c.396A>G (p.Lys132=) | |
| 18 | g.62360039A>T | CA402613822 | TNFRSF11A | c.606A>T (p.Lys202Asn) n.524A>T c.564A>T (p.Lys188Asn) c.621A>T (p.Lys207Asn) c.498A>T (p.Lys166Asn) n.636A>T c.456A>T (p.Lys152Asn) c.396A>T (p.Lys132Asn) | |
| 18 | g.62360040C>A | CA402613824 | TNFRSF11A | c.607C>A (p.Pro203Thr) n.525C>A c.565C>A (p.Pro189Thr) c.622C>A (p.Pro208Thr) c.499C>A (p.Pro167Thr) n.637C>A c.457C>A (p.Pro153Thr) c.397C>A (p.Pro133Thr) | dbSNP gnomAD v3 gnomAD v4 |
| 18 | g.62360040C= | CA2308285241 | TNFRSF11A | c.607C= (p.Pro203=) n.525C= c.565C= (p.Pro189=) c.622C= (p.Pro208=) c.499C= (p.Pro167=) n.637C= c.457C= (p.Pro153=) c.397C= (p.Pro133=) | |
| 18 | g.62360040C>G | CA402613825 | TNFRSF11A | c.607C>G (p.Pro203Ala) n.525C>G c.565C>G (p.Pro189Ala) c.622C>G (p.Pro208Ala) c.499C>G (p.Pro167Ala) n.637C>G c.457C>G (p.Pro153Ala) c.397C>G (p.Pro133Ala) | |
| 18 | g.62360040C>T | CA402613827 | TNFRSF11A | c.607C>T (p.Pro203Ser) n.525C>T c.565C>T (p.Pro189Ser) c.622C>T (p.Pro208Ser) c.499C>T (p.Pro167Ser) n.637C>T c.457C>T (p.Pro153Ser) c.397C>T (p.Pro133Ser) | |
| 18 | g.62360041C>A | CA402613829 | TNFRSF11A | c.608C>A (p.Pro203Gln) n.526C>A c.566C>A (p.Pro189Gln) c.623C>A (p.Pro208Gln) c.500C>A (p.Pro167Gln) n.638C>A c.458C>A (p.Pro153Gln) c.398C>A (p.Pro133Gln) | gnomAD v4 |
| 18 | g.62360041C= | CA2308285242 | TNFRSF11A | c.608C= (p.Pro203=) n.526C= c.566C= (p.Pro189=) c.623C= (p.Pro208=) c.500C= (p.Pro167=) n.638C= c.458C= (p.Pro153=) c.398C= (p.Pro133=) | |
| 18 | g.62360041C>G | CA402613831 | TNFRSF11A | c.608C>G (p.Pro203Arg) n.526C>G c.566C>G (p.Pro189Arg) c.623C>G (p.Pro208Arg) c.500C>G (p.Pro167Arg) n.638C>G c.458C>G (p.Pro153Arg) c.398C>G (p.Pro133Arg) | |
| 18 | g.62360041C>T | CA402613832 | TNFRSF11A | c.608C>T (p.Pro203Leu) n.526C>T c.566C>T (p.Pro189Leu) c.623C>T (p.Pro208Leu) c.500C>T (p.Pro167Leu) n.638C>T c.458C>T (p.Pro153Leu) c.398C>T (p.Pro133Leu) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 18 | g.62360042A>C | CA504079216 | TNFRSF11A | c.609A>C (p.Pro203=) n.527A>C c.567A>C (p.Pro189=) c.624A>C (p.Pro208=) c.501A>C (p.Pro167=) n.639A>C c.459A>C (p.Pro153=) c.399A>C (p.Pro133=) | |
| 18 | g.62360042A>G | CA504079219 | TNFRSF11A | c.609A>G (p.Pro203=) n.527A>G c.567A>G (p.Pro189=) c.624A>G (p.Pro208=) c.501A>G (p.Pro167=) n.639A>G c.459A>G (p.Pro153=) c.399A>G (p.Pro133=) | |
| 18 | g.62360042A>T | CA504079217 | TNFRSF11A | c.609A>T (p.Pro203=) n.527A>T c.567A>T (p.Pro189=) c.624A>T (p.Pro208=) c.501A>T (p.Pro167=) n.639A>T c.459A>T (p.Pro153=) c.399A>T (p.Pro133=) | |
| 18 | g.62360043C>A | CA402613834 | TNFRSF11A | c.610C>A (p.Pro204Thr) n.528C>A c.568C>A (p.Pro190Thr) c.625C>A (p.Pro209Thr) c.502C>A (p.Pro168Thr) n.640C>A c.460C>A (p.Pro154Thr) c.400C>A (p.Pro134Thr) | |
| 18 | g.62360043C= | CA2308285243 | TNFRSF11A | c.610C= (p.Pro204=) n.528C= c.568C= (p.Pro190=) c.625C= (p.Pro209=) c.502C= (p.Pro168=) n.640C= c.460C= (p.Pro154=) c.400C= (p.Pro134=) | |
| 18 | g.62360043C>G | CA402613835 | TNFRSF11A | c.610C>G (p.Pro204Ala) n.528C>G c.568C>G (p.Pro190Ala) c.625C>G (p.Pro209Ala) c.502C>G (p.Pro168Ala) n.640C>G c.460C>G (p.Pro154Ala) c.400C>G (p.Pro134Ala) | |
| 18 | g.62360043C>T | CA402613837 | TNFRSF11A | c.610C>T (p.Pro204Ser) n.528C>T c.568C>T (p.Pro190Ser) c.625C>T (p.Pro209Ser) c.502C>T (p.Pro168Ser) n.640C>T c.460C>T (p.Pro154Ser) c.400C>T (p.Pro134Ser) | gnomAD v4 |
| 18 | g.62360043_62360044insTAAATGGT | CA630114347 | TNFRSF11A | c.610_611insTAAATGGT (p.Pro204LeufsTer14) c.610_611insTAAATGGT (p.Pro204LeufsTer8) c.568_569insTAAATGGT (p.Pro190LeufsTer14) c.625_626insTAAATGGT (p.Pro209LeufsTer14) c.502_503insTAAATGGT (p.Pro168LeufsTer14) n.640_641insTAAATGGT c.460_461insTAAATGGT (p.Pro154LeufsTer14) c.400_401insTAAATGGT (p.Pro134LeufsTer14) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 18 | g.62360044C>A | CA402613842 | TNFRSF11A | c.611C>A (p.Pro204Gln) c.569C>A (p.Pro190Gln) c.626C>A (p.Pro209Gln) c.503C>A (p.Pro168Gln) n.641C>A c.461C>A (p.Pro154Gln) c.401C>A (p.Pro134Gln) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 18 | g.62360044C= | CA2308285244 | TNFRSF11A | c.611C= (p.Pro204=) c.569C= (p.Pro190=) c.626C= (p.Pro209=) c.503C= (p.Pro168=) n.641C= c.461C= (p.Pro154=) c.401C= (p.Pro134=) | |
| 18 | g.62360044C>G | CA402613840 | TNFRSF11A | c.611C>G (p.Pro204Arg) c.569C>G (p.Pro190Arg) c.626C>G (p.Pro209Arg) c.503C>G (p.Pro168Arg) n.641C>G c.461C>G (p.Pro154Arg) c.401C>G (p.Pro134Arg) | |
| 18 | g.62360044C>T | CA402613839 | TNFRSF11A | c.611C>T (p.Pro204Leu) c.569C>T (p.Pro190Leu) c.626C>T (p.Pro209Leu) c.503C>T (p.Pro168Leu) n.641C>T c.461C>T (p.Pro154Leu) c.401C>T (p.Pro134Leu) | dbSNP |
| 18 | g.62360045A>C | CA504079228 | TNFRSF11A | c.612A>C (p.Pro204=) c.570A>C (p.Pro190=) c.627A>C (p.Pro209=) c.504A>C (p.Pro168=) n.642A>C c.462A>C (p.Pro154=) c.402A>C (p.Pro134=) | |
| 18 | g.62360045A>G | CA504079230 | TNFRSF11A | c.612A>G (p.Pro204=) c.570A>G (p.Pro190=) c.627A>G (p.Pro209=) c.504A>G (p.Pro168=) n.642A>G c.462A>G (p.Pro154=) c.402A>G (p.Pro134=) | |
| 18 | g.62360045A>T | CA504079232 | TNFRSF11A | c.612A>T (p.Pro204=) c.570A>T (p.Pro190=) c.627A>T (p.Pro209=) c.504A>T (p.Pro168=) n.642A>T c.462A>T (p.Pro154=) c.402A>T (p.Pro134=) | |
| 18 | g.62360046A>C | CA402613844 | TNFRSF11A | c.613A>C (p.Asn205His) c.571A>C (p.Asn191His) c.628A>C (p.Asn210His) c.505A>C (p.Asn169His) n.643A>C c.463A>C (p.Asn155His) c.403A>C (p.Asn135His) | |
| 18 | g.62360046A>G | CA402613845 | TNFRSF11A | c.613A>G (p.Asn205Asp) c.571A>G (p.Asn191Asp) c.628A>G (p.Asn210Asp) c.505A>G (p.Asn169Asp) n.643A>G c.463A>G (p.Asn155Asp) c.403A>G (p.Asn135Asp) | |
| 18 | g.62360046A>T | CA402613846 | TNFRSF11A | c.613A>T (p.Asn205Tyr) c.571A>T (p.Asn191Tyr) c.628A>T (p.Asn210Tyr) c.505A>T (p.Asn169Tyr) n.643A>T c.463A>T (p.Asn155Tyr) c.403A>T (p.Asn135Tyr) | |
| 18 | g.62360047A>C | CA402613848 | TNFRSF11A | c.614A>C (p.Asn205Thr) c.572A>C (p.Asn191Thr) c.629A>C (p.Asn210Thr) c.506A>C (p.Asn169Thr) n.644A>C c.464A>C (p.Asn155Thr) c.404A>C (p.Asn135Thr) | |
| 18 | g.62360047A>G | CA402613850 | TNFRSF11A | c.614A>G (p.Asn205Ser) c.572A>G (p.Asn191Ser) c.629A>G (p.Asn210Ser) c.506A>G (p.Asn169Ser) n.644A>G c.464A>G (p.Asn155Ser) c.404A>G (p.Asn135Ser) | |
| 18 | g.62360047A>T | CA402613852 | TNFRSF11A | c.614A>T (p.Asn205Ile) c.572A>T (p.Asn191Ile) c.629A>T (p.Asn210Ile) c.506A>T (p.Asn169Ile) n.644A>T c.464A>T (p.Asn155Ile) c.404A>T (p.Asn135Ile) | |
| 18 | g.62360048T>A | CA402613853 | TNFRSF11A | c.615T>A (p.Asn205Lys) c.573T>A (p.Asn191Lys) c.630T>A (p.Asn210Lys) c.507T>A (p.Asn169Lys) n.645T>A c.465T>A (p.Asn155Lys) c.405T>A (p.Asn135Lys) | |
| 18 | g.62360048T>C | CA504079244 | TNFRSF11A | c.615T>C (p.Asn205=) c.573T>C (p.Asn191=) c.630T>C (p.Asn210=) c.507T>C (p.Asn169=) n.645T>C c.465T>C (p.Asn155=) c.405T>C (p.Asn135=) | gnomAD v4 |
| 18 | g.62360048T>G | CA402613855 | TNFRSF11A | c.615T>G (p.Asn205Lys) c.573T>G (p.Asn191Lys) c.630T>G (p.Asn210Lys) c.507T>G (p.Asn169Lys) n.645T>G c.465T>G (p.Asn155Lys) c.405T>G (p.Asn135Lys) | |
| 18 | g.62360049G>A | CA402613857 | TNFRSF11A | c.616G>A (p.Glu206Lys) c.616G>A (p.Gly206Arg) c.574G>A (p.Glu192Lys) c.631G>A (p.Glu211Lys) c.508G>A (p.Glu170Lys) n.646G>A c.466G>A (p.Glu156Lys) c.406G>A (p.Glu136Lys) | |
| 18 | g.62360049G>C | CA402613859 | TNFRSF11A | c.616G>C (p.Glu206Gln) c.616G>C (p.Gly206Arg) c.574G>C (p.Glu192Gln) c.631G>C (p.Glu211Gln) c.508G>C (p.Glu170Gln) n.646G>C c.466G>C (p.Glu156Gln) c.406G>C (p.Glu136Gln) | |
| 18 | g.62360049G>T | CA402613861 | TNFRSF11A | c.616G>T (p.Glu206Ter) c.616G>T (p.Gly206Ter) c.574G>T (p.Glu192Ter) c.631G>T (p.Glu211Ter) c.508G>T (p.Glu170Ter) n.646G>T c.466G>T (p.Glu156Ter) c.406G>T (p.Glu136Ter) | |
| 18 | g.62360050G>A | CA402613866 | TNFRSF11A | c.616+1G>A (n.616+1G>A) c.574+1G>A (n.574+1G>A) c.631+1G>A (n.631+1G>A) c.508+1G>A (n.508+1G>A) n.646+1G>A c.466+1G>A (n.466+1G>A) c.406+1G>A (n.406+1G>A) | |
| 18 | g.62360050G>C | CA402613865 | TNFRSF11A | c.616+1G>C (n.616+1G>C) c.574+1G>C (n.574+1G>C) c.631+1G>C (n.631+1G>C) c.508+1G>C (n.508+1G>C) n.646+1G>C c.466+1G>C (n.466+1G>C) c.406+1G>C (n.406+1G>C) | dbSNP |
| 18 | g.62360050G= | CA2308285245 | TNFRSF11A | c.616+1G= (n.616+1G=) c.574+1G= (n.574+1G=) c.631+1G= (n.631+1G=) c.508+1G= (n.508+1G=) n.646+1G= c.466+1G= (n.466+1G=) c.406+1G= (n.406+1G=) | |
| 18 | g.62360050G>T | CA402613863 | TNFRSF11A | c.616+1G>T (n.616+1G>T) c.574+1G>T (n.574+1G>T) c.631+1G>T (n.631+1G>T) c.508+1G>T (n.508+1G>T) n.646+1G>T c.466+1G>T (n.466+1G>T) c.406+1G>T (n.406+1G>T) | |
| 18 | g.62360051T>A | CA402613868 | TNFRSF11A | c.616+2T>A (n.616+2T>A) c.574+2T>A (n.574+2T>A) c.631+2T>A (n.631+2T>A) c.508+2T>A (n.508+2T>A) n.646+2T>A c.466+2T>A (n.466+2T>A) c.406+2T>A (n.406+2T>A) | |
| 18 | g.62360051T>C | CA402613869 | TNFRSF11A | c.616+2T>C (n.616+2T>C) c.574+2T>C (n.574+2T>C) c.631+2T>C (n.631+2T>C) c.508+2T>C (n.508+2T>C) n.646+2T>C c.466+2T>C (n.466+2T>C) c.406+2T>C (n.406+2T>C) | |
| 18 | g.62360051T>G | CA402613871 | TNFRSF11A | c.616+2T>G (n.616+2T>G) c.574+2T>G (n.574+2T>G) c.631+2T>G (n.631+2T>G) c.508+2T>G (n.508+2T>G) n.646+2T>G c.466+2T>G (n.466+2T>G) c.406+2T>G (n.406+2T>G) | |
| 18 | g.62360052A>G | CA2695227696 | TNFRSF11A | c.616+3A>G (n.616+3A>G) c.574+3A>G (n.574+3A>G) c.631+3A>G (n.631+3A>G) c.508+3A>G (n.508+3A>G) n.646+3A>G c.466+3A>G (n.466+3A>G) c.406+3A>G (n.406+3A>G) | |
| 18 | g.62360053T>A | CA8983805 | TNFRSF11A | c.616+4T>A (n.616+4T>A) c.574+4T>A (n.574+4T>A) c.631+4T>A (n.631+4T>A) c.508+4T>A (n.508+4T>A) n.646+4T>A c.466+4T>A (n.466+4T>A) c.406+4T>A (n.406+4T>A) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 18 | g.62360053T>C | CA8983804 | TNFRSF11A | c.616+4T>C (n.616+4T>C) c.574+4T>C (n.574+4T>C) c.631+4T>C (n.631+4T>C) c.508+4T>C (n.508+4T>C) n.646+4T>C c.466+4T>C (n.466+4T>C) c.406+4T>C (n.406+4T>C) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 18 | g.62360053T>G | CA630114348 | TNFRSF11A | c.616+4T>G (n.616+4T>G) c.574+4T>G (n.574+4T>G) c.631+4T>G (n.631+4T>G) c.508+4T>G (n.508+4T>G) n.646+4T>G c.466+4T>G (n.466+4T>G) c.406+4T>G (n.406+4T>G) | dbSNP gnomAD v2 |
| 18 | g.62360053T= | CA2308285246 | TNFRSF11A | c.616+4T= (n.616+4T=) c.574+4T= (n.574+4T=) c.631+4T= (n.631+4T=) c.508+4T= (n.508+4T=) n.646+4T= c.466+4T= (n.466+4T=) c.406+4T= (n.406+4T=) | |
| 18 | g.62360055T= | CA2308285247 | TNFRSF11A | c.616+6T= (n.616+6T=) c.574+6T= (n.574+6T=) c.631+6T= (n.631+6T=) c.508+6T= (n.508+6T=) n.646+6T= c.466+6T= (n.466+6T=) c.406+6T= (n.406+6T=) | |
| 18 | g.62360055_62360056insGCGAATTTCGACGATCGTTGCATTAACTCGCGAACAAACGGA | CA630114349 | TNFRSF11A | c.616+6_616+7insGCGAATTTCGACGATCGTTGCATTAACTCGCGAACAAACGGA (n.616+6_616+7insGCGAATTTCGACGATCGTTGCATTAACTCGCGAACAAACGGA) c.574+6_574+7insGCGAATTTCGACGATCGTTGCATTAACTCGCGAACAAACGGA (n.574+6_574+7insGCGAATTTCGACGATCGTTGCATTAACTCGCGAACAAACGGA) c.631+6_631+7insGCGAATTTCGACGATCGTTGCATTAACTCGCGAACAAACGGA (n.631+6_631+7insGCGAATTTCGACGATCGTTGCATTAACTCGCGAACAAACGGA) c.508+6_508+7insGCGAATTTCGACGATCGTTGCATTAACTCGCGAACAAACGGA (n.508+6_508+7insGCGAATTTCGACGATCGTTGCATTAACTCGCGAACAAACGGA) n.646+6_646+7insGCGAATTTCGACGATCGTTGCATTAACTCGCGAACAAACGGA c.466+6_466+7insGCGAATTTCGACGATCGTTGCATTAACTCGCGAACAAACGGA (n.466+6_466+7insGCGAATTTCGACGATCGTTGCATTAACTCGCGAACAAACGGA) c.406+6_406+7insGCGAATTTCGACGATCGTTGCATTAACTCGCGAACAAACGGA (n.406+6_406+7insGCGAATTTCGACGATCGTTGCATTAACTCGCGAACAAACGGA) | dbSNP gnomAD v2 |