| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 18 | g.62358328A= | CA2308284534 | TNFRSF11A | c.508A= (p.Arg170=) n.426A= c.466A= (p.Arg156=) c.523A= (p.Arg175=) c.400A= (p.Arg134=) n.538A= c.358A= (p.Arg120=) c.298A= (p.Arg100=) | |
| 18 | g.62358328A>C | CA504078186 | TNFRSF11A | c.508A>C (p.Arg170=) n.426A>C c.466A>C (p.Arg156=) c.523A>C (p.Arg175=) c.400A>C (p.Arg134=) n.538A>C c.358A>C (p.Arg120=) c.298A>C (p.Arg100=) | |
| 18 | g.62358328A>G | CA118112 | TNFRSF11A | c.508A>G (p.Arg170Gly) n.426A>G c.466A>G (p.Arg156Gly) c.523A>G (p.Arg175Gly) c.400A>G (p.Arg134Gly) n.538A>G c.358A>G (p.Arg120Gly) c.298A>G (p.Arg100Gly) | ClinVar dbSNP gnomAD v4 |
| 18 | g.62358328A>T | CA402613406 | TNFRSF11A | c.508A>T (p.Arg170Ter) n.426A>T c.466A>T (p.Arg156Ter) c.523A>T (p.Arg175Ter) c.400A>T (p.Arg134Ter) n.538A>T c.358A>T (p.Arg120Ter) c.298A>T (p.Arg100Ter) | |
| 18 | g.62358329G>A | CA402613409 | TNFRSF11A | c.509G>A (p.Arg170Lys) n.427G>A c.467G>A (p.Arg156Lys) c.524G>A (p.Arg175Lys) c.401G>A (p.Arg134Lys) n.539G>A c.359G>A (p.Arg120Lys) c.299G>A (p.Arg100Lys) | |
| 18 | g.62358329G>C | CA402613410 | TNFRSF11A | c.509G>C (p.Arg170Thr) n.427G>C c.467G>C (p.Arg156Thr) c.524G>C (p.Arg175Thr) c.401G>C (p.Arg134Thr) n.539G>C c.359G>C (p.Arg120Thr) c.299G>C (p.Arg100Thr) | |
| 18 | g.62358329G>T | CA402613413 | TNFRSF11A | c.509G>T (p.Arg170Ile) n.427G>T c.467G>T (p.Arg156Ile) c.524G>T (p.Arg175Ile) c.401G>T (p.Arg134Ile) n.539G>T c.359G>T (p.Arg120Ile) c.299G>T (p.Arg100Ile) | gnomAD v4 |
| 18 | g.62358330A>C | CA402613417 | TNFRSF11A | c.510A>C (p.Arg170Ser) n.428A>C c.468A>C (p.Arg156Ser) c.525A>C (p.Arg175Ser) c.402A>C (p.Arg134Ser) n.540A>C c.360A>C (p.Arg120Ser) c.300A>C (p.Arg100Ser) | |
| 18 | g.62358330A>G | CA504078196 | TNFRSF11A | c.510A>G (p.Arg170=) n.428A>G c.468A>G (p.Arg156=) c.525A>G (p.Arg175=) c.402A>G (p.Arg134=) n.540A>G c.360A>G (p.Arg120=) c.300A>G (p.Arg100=) | |
| 18 | g.62358330A>T | CA402613420 | TNFRSF11A | c.510A>T (p.Arg170Ser) n.428A>T c.468A>T (p.Arg156Ser) c.525A>T (p.Arg175Ser) c.402A>T (p.Arg134Ser) n.540A>T c.360A>T (p.Arg120Ser) c.300A>T (p.Arg100Ser) | |
| 18 | g.62358331C>A | CA402613426 | TNFRSF11A | c.511C>A (p.Pro171Thr) n.429C>A c.469C>A (p.Pro157Thr) c.526C>A (p.Pro176Thr) c.403C>A (p.Pro135Thr) n.541C>A c.361C>A (p.Pro121Thr) c.301C>A (p.Pro101Thr) | |
| 18 | g.62358331C>G | CA402613427 | TNFRSF11A | c.511C>G (p.Pro171Ala) n.429C>G c.469C>G (p.Pro157Ala) c.526C>G (p.Pro176Ala) c.403C>G (p.Pro135Ala) n.541C>G c.361C>G (p.Pro121Ala) c.301C>G (p.Pro101Ala) | |
| 18 | g.62358331C>T | CA402613422 | TNFRSF11A | c.511C>T (p.Pro171Ser) n.429C>T c.469C>T (p.Pro157Ser) c.526C>T (p.Pro176Ser) c.403C>T (p.Pro135Ser) n.541C>T c.361C>T (p.Pro121Ser) c.301C>T (p.Pro101Ser) | |
| 18 | g.62358332C>A | CA402613433 | TNFRSF11A | c.512C>A (p.Pro171His) n.430C>A c.470C>A (p.Pro157His) c.527C>A (p.Pro176His) c.404C>A (p.Pro135His) n.542C>A c.362C>A (p.Pro121His) c.302C>A (p.Pro101His) | |
| 18 | g.62358332C>G | CA402613430 | TNFRSF11A | c.512C>G (p.Pro171Arg) n.430C>G c.470C>G (p.Pro157Arg) c.527C>G (p.Pro176Arg) c.404C>G (p.Pro135Arg) n.542C>G c.362C>G (p.Pro121Arg) c.302C>G (p.Pro101Arg) | |
| 18 | g.62358332C>T | CA402613436 | TNFRSF11A | c.512C>T (p.Pro171Leu) n.430C>T c.470C>T (p.Pro157Leu) c.527C>T (p.Pro176Leu) c.404C>T (p.Pro135Leu) n.542C>T c.362C>T (p.Pro121Leu) c.302C>T (p.Pro101Leu) | gnomAD v4 |
| 18 | g.62358333C>A | CA504078206 | TNFRSF11A | c.513C>A (p.Pro171=) n.431C>A c.471C>A (p.Pro157=) c.528C>A (p.Pro176=) c.405C>A (p.Pro135=) n.543C>A c.363C>A (p.Pro121=) c.303C>A (p.Pro101=) | |
| 18 | g.62358333C= | CA2308284535 | TNFRSF11A | c.513C= (p.Pro171=) n.431C= c.471C= (p.Pro157=) c.528C= (p.Pro176=) c.405C= (p.Pro135=) n.543C= c.363C= (p.Pro121=) c.303C= (p.Pro101=) | |
| 18 | g.62358333C>G | CA504078208 | TNFRSF11A | c.513C>G (p.Pro171=) n.431C>G c.471C>G (p.Pro157=) c.528C>G (p.Pro176=) c.405C>G (p.Pro135=) n.543C>G c.363C>G (p.Pro121=) c.303C>G (p.Pro101=) | |
| 18 | g.62358333C>T | CA504078210 | TNFRSF11A | c.513C>T (p.Pro171=) n.431C>T c.471C>T (p.Pro157=) c.528C>T (p.Pro176=) c.405C>T (p.Pro135=) n.543C>T c.363C>T (p.Pro121=) c.303C>T (p.Pro101=) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 18 | g.62358334T>A | CA402613441 | TNFRSF11A | c.514T>A (p.Trp172Arg) n.432T>A c.472T>A (p.Trp158Arg) c.529T>A (p.Trp177Arg) c.406T>A (p.Trp136Arg) n.544T>A c.364T>A (p.Trp122Arg) c.304T>A (p.Trp102Arg) | |
| 18 | g.62358334T>C | CA402613445 | TNFRSF11A | c.514T>C (p.Trp172Arg) n.432T>C c.472T>C (p.Trp158Arg) c.529T>C (p.Trp177Arg) c.406T>C (p.Trp136Arg) n.544T>C c.364T>C (p.Trp122Arg) c.304T>C (p.Trp102Arg) | gnomAD v4 |
| 18 | g.62358334T>G | CA402613442 | TNFRSF11A | c.514T>G (p.Trp172Gly) n.432T>G c.472T>G (p.Trp158Gly) c.529T>G (p.Trp177Gly) c.406T>G (p.Trp136Gly) n.544T>G c.364T>G (p.Trp122Gly) c.304T>G (p.Trp102Gly) | |
| 18 | g.62358335G>A | CA402613449 | TNFRSF11A | c.515G>A (p.Trp172Ter) n.433G>A c.473G>A (p.Trp158Ter) c.530G>A (p.Trp177Ter) c.407G>A (p.Trp136Ter) n.545G>A c.365G>A (p.Trp122Ter) c.305G>A (p.Trp102Ter) | |
| 18 | g.62358335G>C | CA402613450 | TNFRSF11A | c.515G>C (p.Trp172Ser) n.433G>C c.473G>C (p.Trp158Ser) c.530G>C (p.Trp177Ser) c.407G>C (p.Trp136Ser) n.545G>C c.365G>C (p.Trp122Ser) c.305G>C (p.Trp102Ser) | |
| 18 | g.62358335G>T | CA402613452 | TNFRSF11A | c.515G>T (p.Trp172Leu) n.433G>T c.473G>T (p.Trp158Leu) c.530G>T (p.Trp177Leu) c.407G>T (p.Trp136Leu) n.545G>T c.365G>T (p.Trp122Leu) c.305G>T (p.Trp102Leu) | gnomAD v4 |
| 18 | g.62358336G>A | CA402613454 | TNFRSF11A | c.516G>A (p.Trp172Ter) n.434G>A c.474G>A (p.Trp158Ter) c.531G>A (p.Trp177Ter) c.408G>A (p.Trp136Ter) n.546G>A c.366G>A (p.Trp122Ter) c.306G>A (p.Trp102Ter) | |
| 18 | g.62358336G>C | CA402613456 | TNFRSF11A | c.516G>C (p.Trp172Cys) n.434G>C c.474G>C (p.Trp158Cys) c.531G>C (p.Trp177Cys) c.408G>C (p.Trp136Cys) n.546G>C c.366G>C (p.Trp122Cys) c.306G>C (p.Trp102Cys) | |
| 18 | g.62358336G>T | CA402613457 | TNFRSF11A | c.516G>T (p.Trp172Cys) n.434G>T c.474G>T (p.Trp158Cys) c.531G>T (p.Trp177Cys) c.408G>T (p.Trp136Cys) n.546G>T c.366G>T (p.Trp122Cys) c.306G>T (p.Trp102Cys) | gnomAD v4 |
| 18 | g.62358337A>C | CA402613459 | TNFRSF11A | c.517A>C (p.Thr173Pro) n.435A>C c.475A>C (p.Thr159Pro) c.532A>C (p.Thr178Pro) c.409A>C (p.Thr137Pro) n.547A>C c.367A>C (p.Thr123Pro) c.307A>C (p.Thr103Pro) | |
| 18 | g.62358337A>G | CA402613460 | TNFRSF11A | c.517A>G (p.Thr173Ala) n.435A>G c.475A>G (p.Thr159Ala) c.532A>G (p.Thr178Ala) c.409A>G (p.Thr137Ala) n.547A>G c.367A>G (p.Thr123Ala) c.307A>G (p.Thr103Ala) | COSMIC |
| 18 | g.62358337A>T | CA402613462 | TNFRSF11A | c.517A>T (p.Thr173Ser) n.435A>T c.475A>T (p.Thr159Ser) c.532A>T (p.Thr178Ser) c.409A>T (p.Thr137Ser) n.547A>T c.367A>T (p.Thr123Ser) c.307A>T (p.Thr103Ser) | |
| 18 | g.62358338C>A | CA402613463 | TNFRSF11A | c.518C>A (p.Thr173Asn) n.436C>A c.476C>A (p.Thr159Asn) c.533C>A (p.Thr178Asn) c.410C>A (p.Thr137Asn) n.548C>A c.368C>A (p.Thr123Asn) c.308C>A (p.Thr103Asn) | |
| 18 | g.62358338C= | CA2308284536 | TNFRSF11A | c.518C= (p.Thr173=) n.436C= c.476C= (p.Thr159=) c.533C= (p.Thr178=) c.410C= (p.Thr137=) n.548C= c.368C= (p.Thr123=) c.308C= (p.Thr103=) | |
| 18 | g.62358338C>G | CA402613464 | TNFRSF11A | c.518C>G (p.Thr173Ser) n.436C>G c.476C>G (p.Thr159Ser) c.533C>G (p.Thr178Ser) c.410C>G (p.Thr137Ser) n.548C>G c.368C>G (p.Thr123Ser) c.308C>G (p.Thr103Ser) | |
| 18 | g.62358338C>T | CA402613465 | TNFRSF11A | c.518C>T (p.Thr173Ile) n.436C>T c.476C>T (p.Thr159Ile) c.533C>T (p.Thr178Ile) c.410C>T (p.Thr137Ile) n.548C>T c.368C>T (p.Thr123Ile) c.308C>T (p.Thr103Ile) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 18 | g.62358339C>A | CA504078226 | TNFRSF11A | c.519C>A (p.Thr173=) n.437C>A c.477C>A (p.Thr159=) c.534C>A (p.Thr178=) c.411C>A (p.Thr137=) n.549C>A c.369C>A (p.Thr123=) c.309C>A (p.Thr103=) | |
| 18 | g.62358339C>G | CA504078228 | TNFRSF11A | c.519C>G (p.Thr173=) n.437C>G c.477C>G (p.Thr159=) c.534C>G (p.Thr178=) c.411C>G (p.Thr137=) n.549C>G c.369C>G (p.Thr123=) c.309C>G (p.Thr103=) | |
| 18 | g.62358339C>T | CA504078231 | TNFRSF11A | c.519C>T (p.Thr173=) n.437C>T c.477C>T (p.Thr159=) c.534C>T (p.Thr178=) c.411C>T (p.Thr137=) n.549C>T c.369C>T (p.Thr123=) c.309C>T (p.Thr103=) | |
| 18 | g.62358340A>C | CA402613471 | TNFRSF11A | c.520A>C (p.Asn174His) n.438A>C c.478A>C (p.Asn160His) c.535A>C (p.Asn179His) c.412A>C (p.Asn138His) n.550A>C c.370A>C (p.Asn124His) c.310A>C (p.Asn104His) | |
| 18 | g.62358340A>G | CA402613468 | TNFRSF11A | c.520A>G (p.Asn174Asp) n.438A>G c.478A>G (p.Asn160Asp) c.535A>G (p.Asn179Asp) c.412A>G (p.Asn138Asp) n.550A>G c.370A>G (p.Asn124Asp) c.310A>G (p.Asn104Asp) | |
| 18 | g.62358340A>T | CA402613470 | TNFRSF11A | c.520A>T (p.Asn174Tyr) n.438A>T c.478A>T (p.Asn160Tyr) c.535A>T (p.Asn179Tyr) c.412A>T (p.Asn138Tyr) n.550A>T c.370A>T (p.Asn124Tyr) c.310A>T (p.Asn104Tyr) | |
| 18 | g.62358341A>C | CA402613473 | TNFRSF11A | c.521A>C (p.Asn174Thr) n.439A>C c.479A>C (p.Asn160Thr) c.536A>C (p.Asn179Thr) c.413A>C (p.Asn138Thr) n.551A>C c.371A>C (p.Asn124Thr) c.311A>C (p.Asn104Thr) | |
| 18 | g.62358341A>G | CA402613475 | TNFRSF11A | c.521A>G (p.Asn174Ser) n.439A>G c.479A>G (p.Asn160Ser) c.536A>G (p.Asn179Ser) c.413A>G (p.Asn138Ser) n.551A>G c.371A>G (p.Asn124Ser) c.311A>G (p.Asn104Ser) | |
| 18 | g.62358341A>T | CA402613477 | TNFRSF11A | c.521A>T (p.Asn174Ile) n.439A>T c.479A>T (p.Asn160Ile) c.536A>T (p.Asn179Ile) c.413A>T (p.Asn138Ile) n.551A>T c.371A>T (p.Asn124Ile) c.311A>T (p.Asn104Ile) | |
| 18 | g.62358342G>A | CA402613478 | TNFRSF11A | c.521+1G>A (n.521+1G>A) n.439+1G>A c.479+1G>A (n.479+1G>A) c.536+1G>A (n.536+1G>A) c.413+1G>A (n.413+1G>A) n.551+1G>A c.371+1G>A (n.371+1G>A) c.311+1G>A (n.311+1G>A) | |
| 18 | g.62358342G>C | CA402613479 | TNFRSF11A | c.521+1G>C (n.521+1G>C) n.439+1G>C c.479+1G>C (n.479+1G>C) c.536+1G>C (n.536+1G>C) c.413+1G>C (n.413+1G>C) n.551+1G>C c.371+1G>C (n.371+1G>C) c.311+1G>C (n.311+1G>C) | |
| 18 | g.62358342G>T | CA402613481 | TNFRSF11A | c.521+1G>T (n.521+1G>T) n.439+1G>T c.479+1G>T (n.479+1G>T) c.536+1G>T (n.536+1G>T) c.413+1G>T (n.413+1G>T) n.551+1G>T c.371+1G>T (n.371+1G>T) c.311+1G>T (n.311+1G>T) | |
| 18 | g.62358343T>A | CA402613483 | TNFRSF11A | c.521+2T>A (n.521+2T>A) n.439+2T>A c.479+2T>A (n.479+2T>A) c.536+2T>A (n.536+2T>A) c.413+2T>A (n.413+2T>A) n.551+2T>A c.371+2T>A (n.371+2T>A) c.311+2T>A (n.311+2T>A) | |
| 18 | g.62358343T>C | CA402613484 | TNFRSF11A | c.521+2T>C (n.521+2T>C) n.439+2T>C c.479+2T>C (n.479+2T>C) c.536+2T>C (n.536+2T>C) c.413+2T>C (n.413+2T>C) n.551+2T>C c.371+2T>C (n.371+2T>C) c.311+2T>C (n.311+2T>C) |