| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 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 |
| 18 | g.62360057_62360058delinsTA | CA2308285248 | TNFRSF11A | c.616+8_616+9delinsTA (n.616+8_616+9delinsTA) c.574+8_574+9delinsTA (n.574+8_574+9delinsTA) c.631+8_631+9delinsTA (n.631+8_631+9delinsTA) c.508+8_508+9delinsTA (n.508+8_508+9delinsTA) n.646+8_646+9delinsTA c.466+8_466+9delinsTA (n.466+8_466+9delinsTA) c.406+8_406+9delinsTA (n.406+8_406+9delinsTA) | |
| 18 | g.62360058A= | CA2308285249 | TNFRSF11A | c.616+9A= (n.616+9A=) c.574+9A= (n.574+9A=) c.631+9A= (n.631+9A=) c.508+9A= (n.508+9A=) n.646+9A= c.466+9A= (n.466+9A=) c.406+9A= (n.406+9A=) | |
| 18 | g.62360058A>G | CA8983807 | TNFRSF11A | c.616+9A>G (n.616+9A>G) c.574+9A>G (n.574+9A>G) c.631+9A>G (n.631+9A>G) c.508+9A>G (n.508+9A>G) n.646+9A>G c.466+9A>G (n.466+9A>G) c.406+9A>G (n.406+9A>G) | dbSNP ExAC gnomAD v2 |
| 18 | g.62360058A>T | CA2642068406 | TNFRSF11A | c.616+9A>T (n.616+9A>T) c.574+9A>T (n.574+9A>T) c.631+9A>T (n.631+9A>T) c.508+9A>T (n.508+9A>T) n.646+9A>T c.466+9A>T (n.466+9A>T) c.406+9A>T (n.406+9A>T) | gnomAD v4 |
| 18 | g.62360062del | CA8983806 | TNFRSF11A | c.616+13del (n.616+13del) c.574+13del (n.574+13del) c.631+13del (n.631+13del) c.508+13del (n.508+13del) n.646+13del c.466+13del (n.466+13del) c.406+13del (n.406+13del) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 18 | g.62360064A>G | CA2642068407 | TNFRSF11A | c.616+15A>G (n.616+15A>G) c.574+15A>G (n.574+15A>G) c.631+15A>G (n.631+15A>G) c.508+15A>G (n.508+15A>G) n.646+15A>G c.466+15A>G (n.466+15A>G) c.406+15A>G (n.406+15A>G) | gnomAD v4 |
| 18 | g.62360066C>A | CA2642068408 | TNFRSF11A | c.616+17C>A (n.616+17C>A) c.574+17C>A (n.574+17C>A) c.631+17C>A (n.631+17C>A) c.508+17C>A (n.508+17C>A) n.646+17C>A c.466+17C>A (n.466+17C>A) c.406+17C>A (n.406+17C>A) | gnomAD v4 |
| 18 | g.62360066C= | CA2308285250 | TNFRSF11A | c.616+17C= (n.616+17C=) c.574+17C= (n.574+17C=) c.631+17C= (n.631+17C=) c.508+17C= (n.508+17C=) n.646+17C= c.466+17C= (n.466+17C=) c.406+17C= (n.406+17C=) | |
| 18 | g.62360066C>T | CA301697976 | TNFRSF11A | c.616+17C>T (n.616+17C>T) c.574+17C>T (n.574+17C>T) c.631+17C>T (n.631+17C>T) c.508+17C>T (n.508+17C>T) n.646+17C>T c.466+17C>T (n.466+17C>T) c.406+17C>T (n.406+17C>T) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 18 | g.62360067C>A | CA2642068409 | TNFRSF11A | c.616+18C>A (n.616+18C>A) c.574+18C>A (n.574+18C>A) c.631+18C>A (n.631+18C>A) c.508+18C>A (n.508+18C>A) n.646+18C>A c.466+18C>A (n.466+18C>A) c.406+18C>A (n.406+18C>A) | gnomAD v4 |
| 18 | g.62360067C>G | CA2642068410 | TNFRSF11A | c.616+18C>G (n.616+18C>G) c.574+18C>G (n.574+18C>G) c.631+18C>G (n.631+18C>G) c.508+18C>G (n.508+18C>G) n.646+18C>G c.466+18C>G (n.466+18C>G) c.406+18C>G (n.406+18C>G) | gnomAD v4 |
| 18 | g.62360068T>A | CA2642068411 | TNFRSF11A | c.616+19T>A (n.616+19T>A) c.574+19T>A (n.574+19T>A) c.631+19T>A (n.631+19T>A) c.508+19T>A (n.508+19T>A) n.646+19T>A c.466+19T>A (n.466+19T>A) c.406+19T>A (n.406+19T>A) | gnomAD v4 |
| 18 | g.62360068T>C | CA991036669 | TNFRSF11A | c.616+19T>C (n.616+19T>C) c.574+19T>C (n.574+19T>C) c.631+19T>C (n.631+19T>C) c.508+19T>C (n.508+19T>C) n.646+19T>C c.466+19T>C (n.466+19T>C) c.406+19T>C (n.406+19T>C) | dbSNP gnomAD v3 gnomAD v4 |
| 18 | g.62360068T= | CA2308285251 | TNFRSF11A | c.616+19T= (n.616+19T=) c.574+19T= (n.574+19T=) c.631+19T= (n.631+19T=) c.508+19T= (n.508+19T=) n.646+19T= c.466+19T= (n.466+19T=) c.406+19T= (n.406+19T=) | |
| 18 | g.62360069G>A | CA991036672 | TNFRSF11A | c.616+20G>A (n.616+20G>A) c.574+20G>A (n.574+20G>A) c.631+20G>A (n.631+20G>A) c.508+20G>A (n.508+20G>A) n.646+20G>A c.466+20G>A (n.466+20G>A) c.406+20G>A (n.406+20G>A) | dbSNP gnomAD v3 gnomAD v4 |
| 18 | g.62360069G= | CA2308285252 | TNFRSF11A | c.616+20G= (n.616+20G=) c.574+20G= (n.574+20G=) c.631+20G= (n.631+20G=) c.508+20G= (n.508+20G=) n.646+20G= c.466+20G= (n.466+20G=) c.406+20G= (n.406+20G=) | |
| 18 | g.62360069G>T | CA630114350 | TNFRSF11A | c.616+20G>T (n.616+20G>T) c.574+20G>T (n.574+20G>T) c.631+20G>T (n.631+20G>T) c.508+20G>T (n.508+20G>T) n.646+20G>T c.466+20G>T (n.466+20G>T) c.406+20G>T (n.406+20G>T) | dbSNP gnomAD v2 gnomAD v4 |
| 18 | g.62360070T>C | CA630114351 | TNFRSF11A | c.616+21T>C (n.616+21T>C) c.574+21T>C (n.574+21T>C) c.631+21T>C (n.631+21T>C) c.508+21T>C (n.508+21T>C) n.646+21T>C c.466+21T>C (n.466+21T>C) c.406+21T>C (n.406+21T>C) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 18 | g.62360070T= | CA2308285253 | TNFRSF11A | c.616+21T= (n.616+21T=) c.574+21T= (n.574+21T=) c.631+21T= (n.631+21T=) c.508+21T= (n.508+21T=) n.646+21T= c.466+21T= (n.466+21T=) c.406+21T= (n.406+21T=) | |
| 18 | g.62360071T>G | CA781259622 | TNFRSF11A | c.616+22T>G (n.616+22T>G) c.574+22T>G (n.574+22T>G) c.631+22T>G (n.631+22T>G) c.508+22T>G (n.508+22T>G) n.646+22T>G c.466+22T>G (n.466+22T>G) c.406+22T>G (n.406+22T>G) | dbSNP gnomAD v4 |
| 18 | g.62360071T= | CA2308285254 | TNFRSF11A | c.616+22T= (n.616+22T=) c.574+22T= (n.574+22T=) c.631+22T= (n.631+22T=) c.508+22T= (n.508+22T=) n.646+22T= c.466+22T= (n.466+22T=) c.406+22T= (n.406+22T=) | |
| 18 | g.62360072G>A | CA630114352 | TNFRSF11A | c.616+23G>A (n.616+23G>A) c.574+23G>A (n.574+23G>A) c.631+23G>A (n.631+23G>A) c.508+23G>A (n.508+23G>A) n.646+23G>A c.466+23G>A (n.466+23G>A) c.406+23G>A (n.406+23G>A) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 18 | g.62360072G= | CA2308285255 | TNFRSF11A | c.616+23G= (n.616+23G=) c.574+23G= (n.574+23G=) c.631+23G= (n.631+23G=) c.508+23G= (n.508+23G=) n.646+23G= c.466+23G= (n.466+23G=) c.406+23G= (n.406+23G=) | |
| 18 | g.62360072G>T | CA2642068412 | TNFRSF11A | c.616+23G>T (n.616+23G>T) c.574+23G>T (n.574+23G>T) c.631+23G>T (n.631+23G>T) c.508+23G>T (n.508+23G>T) n.646+23G>T c.466+23G>T (n.466+23G>T) c.406+23G>T (n.406+23G>T) | gnomAD v4 |
| 18 | g.62360073G>A | CA8983808 | TNFRSF11A | c.616+24G>A (n.616+24G>A) c.574+24G>A (n.574+24G>A) c.631+24G>A (n.631+24G>A) c.508+24G>A (n.508+24G>A) n.646+24G>A c.466+24G>A (n.466+24G>A) c.406+24G>A (n.406+24G>A) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 18 | g.62360073G= | CA2308285256 | TNFRSF11A | c.616+24G= (n.616+24G=) c.574+24G= (n.574+24G=) c.631+24G= (n.631+24G=) c.508+24G= (n.508+24G=) n.646+24G= c.466+24G= (n.466+24G=) c.406+24G= (n.406+24G=) | |
| 18 | g.62360074T>C | CA2642068413 | TNFRSF11A | c.616+25T>C (n.616+25T>C) c.574+25T>C (n.574+25T>C) c.631+25T>C (n.631+25T>C) c.508+25T>C (n.508+25T>C) n.646+25T>C c.466+25T>C (n.466+25T>C) c.406+25T>C (n.406+25T>C) | gnomAD v4 |
| 18 | g.62360075T>G | CA2642068414 | TNFRSF11A | c.616+26T>G (n.616+26T>G) c.574+26T>G (n.574+26T>G) c.631+26T>G (n.631+26T>G) c.508+26T>G (n.508+26T>G) n.646+26T>G c.466+26T>G (n.466+26T>G) c.406+26T>G (n.406+26T>G) | gnomAD v4 |
| 18 | g.62360076G>C | CA2642068415 | TNFRSF11A | c.616+27G>C (n.616+27G>C) c.574+27G>C (n.574+27G>C) c.631+27G>C (n.631+27G>C) c.508+27G>C (n.508+27G>C) n.646+27G>C c.466+27G>C (n.466+27G>C) c.406+27G>C (n.406+27G>C) | gnomAD v4 |
| 18 | g.62360078T>C | CA2642068416 | TNFRSF11A | c.616+29T>C (n.616+29T>C) c.574+29T>C (n.574+29T>C) c.631+29T>C (n.631+29T>C) c.508+29T>C (n.508+29T>C) n.646+29T>C c.466+29T>C (n.466+29T>C) c.406+29T>C (n.406+29T>C) | gnomAD v4 |
| 18 | g.62360081A= | CA2308285257 | TNFRSF11A | c.616+32A= (n.616+32A=) c.574+32A= (n.574+32A=) c.631+32A= (n.631+32A=) c.508+32A= (n.508+32A=) n.646+32A= c.466+32A= (n.466+32A=) c.406+32A= (n.406+32A=) | |
| 18 | g.62360081A>G | CA301697993 | TNFRSF11A | c.616+32A>G (n.616+32A>G) c.574+32A>G (n.574+32A>G) c.631+32A>G (n.631+32A>G) c.508+32A>G (n.508+32A>G) n.646+32A>G c.466+32A>G (n.466+32A>G) c.406+32A>G (n.406+32A>G) | dbSNP gnomAD v2 gnomAD v4 |
| 18 | g.62360085G>A | CA630114353 | TNFRSF11A | c.616+36G>A (n.616+36G>A) c.574+36G>A (n.574+36G>A) c.631+36G>A (n.631+36G>A) c.508+36G>A (n.508+36G>A) n.646+36G>A c.466+36G>A (n.466+36G>A) c.406+36G>A (n.406+36G>A) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 18 | g.62360085G>C | CA2642068417 | TNFRSF11A | c.616+36G>C (n.616+36G>C) c.574+36G>C (n.574+36G>C) c.631+36G>C (n.631+36G>C) c.508+36G>C (n.508+36G>C) n.646+36G>C c.466+36G>C (n.466+36G>C) c.406+36G>C (n.406+36G>C) | gnomAD v4 |
| 18 | g.62360085G= | CA2308285258 | TNFRSF11A | c.616+36G= (n.616+36G=) c.574+36G= (n.574+36G=) c.631+36G= (n.631+36G=) c.508+36G= (n.508+36G=) n.646+36G= c.466+36G= (n.466+36G=) c.406+36G= (n.406+36G=) | |
| 18 | g.62360085G>T | CA657410094 | TNFRSF11A | c.616+36G>T (n.616+36G>T) c.574+36G>T (n.574+36G>T) c.631+36G>T (n.631+36G>T) c.508+36G>T (n.508+36G>T) n.646+36G>T c.466+36G>T (n.466+36G>T) c.406+36G>T (n.406+36G>T) | COSMIC |
| 18 | g.62360086C= | CA2308285259 | TNFRSF11A | c.616+37C= (n.616+37C=) c.574+37C= (n.574+37C=) c.631+37C= (n.631+37C=) c.508+37C= (n.508+37C=) n.646+37C= c.466+37C= (n.466+37C=) c.406+37C= (n.406+37C=) | |
| 18 | g.62360086C>T | CA630114354 | TNFRSF11A | c.616+37C>T (n.616+37C>T) c.574+37C>T (n.574+37C>T) c.631+37C>T (n.631+37C>T) c.508+37C>T (n.508+37C>T) n.646+37C>T c.466+37C>T (n.466+37C>T) c.406+37C>T (n.406+37C>T) | dbSNP gnomAD v2 gnomAD v4 |
| 18 | g.62360087C>A | CA2642068418 | TNFRSF11A | c.616+38C>A (n.616+38C>A) c.574+38C>A (n.574+38C>A) c.631+38C>A (n.631+38C>A) c.508+38C>A (n.508+38C>A) n.646+38C>A c.466+38C>A (n.466+38C>A) c.406+38C>A (n.406+38C>A) | gnomAD v4 |
| 18 | g.62360087C>T | CA2642068419 | TNFRSF11A | c.616+38C>T (n.616+38C>T) c.574+38C>T (n.574+38C>T) c.631+38C>T (n.631+38C>T) c.508+38C>T (n.508+38C>T) n.646+38C>T c.466+38C>T (n.466+38C>T) c.406+38C>T (n.406+38C>T) | gnomAD v4 |
| 18 | g.62360089C>A | CA2642068420 | TNFRSF11A | c.616+40C>A (n.616+40C>A) c.574+40C>A (n.574+40C>A) c.631+40C>A (n.631+40C>A) c.508+40C>A (n.508+40C>A) n.646+40C>A c.466+40C>A (n.466+40C>A) c.406+40C>A (n.406+40C>A) | gnomAD v4 |
| 18 | g.62360090A>G | CA2576518653 | TNFRSF11A | c.616+41A>G (n.616+41A>G) c.574+41A>G (n.574+41A>G) c.631+41A>G (n.631+41A>G) c.508+41A>G (n.508+41A>G) n.646+41A>G c.466+41A>G (n.466+41A>G) c.406+41A>G (n.406+41A>G) | |
| 18 | g.62360091G>A | CA2642068424 | TNFRSF11A | c.616+42G>A (n.616+42G>A) c.574+42G>A (n.574+42G>A) c.631+42G>A (n.631+42G>A) c.508+42G>A (n.508+42G>A) n.646+42G>A c.466+42G>A (n.466+42G>A) c.406+42G>A (n.406+42G>A) | gnomAD v4 |
| 18 | g.62360091G>T | CA2642068422 | TNFRSF11A | c.616+42G>T (n.616+42G>T) c.574+42G>T (n.574+42G>T) c.631+42G>T (n.631+42G>T) c.508+42G>T (n.508+42G>T) n.646+42G>T c.466+42G>T (n.466+42G>T) c.406+42G>T (n.406+42G>T) | gnomAD v4 |
| 18 | g.62360093del | CA2642068421 | TNFRSF11A | c.616+44del (n.616+44del) c.574+44del (n.574+44del) c.631+44del (n.631+44del) c.508+44del (n.508+44del) n.646+44del c.466+44del (n.466+44del) c.406+44del (n.406+44del) | gnomAD v4 |
| 18 | g.62360092G>A | CA2308285261 | TNFRSF11A | c.616+43G>A (n.616+43G>A) c.574+43G>A (n.574+43G>A) c.631+43G>A (n.631+43G>A) c.508+43G>A (n.508+43G>A) n.646+43G>A c.466+43G>A (n.466+43G>A) c.406+43G>A (n.406+43G>A) | dbSNP gnomAD v4 |
| 18 | g.62360092G>C | CA2308285260 | TNFRSF11A | c.616+43G>C (n.616+43G>C) c.574+43G>C (n.574+43G>C) c.631+43G>C (n.631+43G>C) c.508+43G>C (n.508+43G>C) n.646+43G>C c.466+43G>C (n.466+43G>C) c.406+43G>C (n.406+43G>C) | dbSNP |
| 18 | g.62360092G= | CA2308285262 | TNFRSF11A | c.616+43G= (n.616+43G=) c.574+43G= (n.574+43G=) c.631+43G= (n.631+43G=) c.508+43G= (n.508+43G=) n.646+43G= c.466+43G= (n.466+43G=) c.406+43G= (n.406+43G=) | |
| 18 | g.62360092G>T | CA630114355 | TNFRSF11A | c.616+43G>T (n.616+43G>T) c.574+43G>T (n.574+43G>T) c.631+43G>T (n.631+43G>T) c.508+43G>T (n.508+43G>T) n.646+43G>T c.466+43G>T (n.466+43G>T) c.406+43G>T (n.406+43G>T) | dbSNP gnomAD v2 gnomAD v4 |
| 18 | g.62360093G>A | CA2642068426 | TNFRSF11A | c.616+44G>A (n.616+44G>A) c.574+44G>A (n.574+44G>A) c.631+44G>A (n.631+44G>A) c.508+44G>A (n.508+44G>A) n.646+44G>A c.466+44G>A (n.466+44G>A) c.406+44G>A (n.406+44G>A) | gnomAD v4 |