UPDATE - Protein Allele ID & Protein Sequence HGVS Requests Partially Restored
Protein allele requests are no longer disabled.
Currently, hypothetical explanatory transcript generation is not part of the response and is being investigated.
Protein allele requests are no longer disabled.
Currently, hypothetical explanatory transcript generation is not part of the response and is being investigated.
| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 13 | g.42606566_42606567del | CA2622837735 | TNFSF11 | c.602_603del (p.Phe201Ter) c.461_462del (p.Phe154Ter) c.383_384del (p.Phe128Ter) c.440_441del (p.Phe147Ter) | gnomAD v4 |
| 13 | g.42606565T>A | CA388221032 | TNFSF11 | c.601T>A (p.Phe201Ile) c.460T>A (p.Phe154Ile) c.382T>A (p.Phe128Ile) c.439T>A (p.Phe147Ile) | |
| 13 | g.42606565T>C | CA388221034 | TNFSF11 | c.601T>C (p.Phe201Leu) c.460T>C (p.Phe154Leu) c.382T>C (p.Phe128Leu) c.439T>C (p.Phe147Leu) | |
| 13 | g.42606565T>G | CA388221036 | TNFSF11 | c.601T>G (p.Phe201Val) c.460T>G (p.Phe154Val) c.382T>G (p.Phe128Val) c.439T>G (p.Phe147Val) | |
| 13 | g.42606566T>A | CA388221037 | TNFSF11 | c.602T>A (p.Phe201Tyr) c.461T>A (p.Phe154Tyr) c.383T>A (p.Phe128Tyr) c.440T>A (p.Phe147Tyr) | |
| 13 | g.42606566T>C | CA388221038 | TNFSF11 | c.602T>C (p.Phe201Ser) c.461T>C (p.Phe154Ser) c.383T>C (p.Phe128Ser) c.440T>C (p.Phe147Ser) | |
| 13 | g.42606566T>G | CA388221040 | TNFSF11 | c.602T>G (p.Phe201Cys) c.461T>G (p.Phe154Cys) c.383T>G (p.Phe128Cys) c.440T>G (p.Phe147Cys) | |
| 13 | g.42606567T>A | CA388221042 | TNFSF11 | c.603T>A (p.Phe201Leu) c.462T>A (p.Phe154Leu) c.384T>A (p.Phe128Leu) c.441T>A (p.Phe147Leu) | |
| 13 | g.42606567T>C | CA249053397 | TNFSF11 | c.603T>C (p.Phe201=) c.462T>C (p.Phe154=) c.384T>C (p.Phe128=) c.441T>C (p.Phe147=) | dbSNP gnomAD v4 |
| 13 | g.42606567T>G | CA388221044 | TNFSF11 | c.603T>G (p.Phe201Leu) c.462T>G (p.Phe154Leu) c.384T>G (p.Phe128Leu) c.441T>G (p.Phe147Leu) | |
| 13 | g.42606567T= | CA2087395065 | TNFSF11 | c.603T= (p.Phe201=) c.462T= (p.Phe154=) c.384T= (p.Phe128=) c.441T= (p.Phe147=) | |
| 13 | g.42606568A>C | CA388221047 | TNFSF11 | c.604A>C (p.Ser202Arg) c.463A>C (p.Ser155Arg) c.385A>C (p.Ser129Arg) c.442A>C (p.Ser148Arg) | |
| 13 | g.42606568A>G | CA388221050 | TNFSF11 | c.604A>G (p.Ser202Gly) c.463A>G (p.Ser155Gly) c.385A>G (p.Ser129Gly) c.442A>G (p.Ser148Gly) | |
| 13 | g.42606568A>T | CA388221049 | TNFSF11 | c.604A>T (p.Ser202Cys) c.463A>T (p.Ser155Cys) c.385A>T (p.Ser129Cys) c.442A>T (p.Ser148Cys) | |
| 13 | g.42606569G>A | CA388221053 | TNFSF11 | c.605G>A (p.Ser202Asn) c.464G>A (p.Ser155Asn) c.386G>A (p.Ser129Asn) c.443G>A (p.Ser148Asn) | |
| 13 | g.42606569G>C | CA388221057 | TNFSF11 | c.605G>C (p.Ser202Thr) c.464G>C (p.Ser155Thr) c.386G>C (p.Ser129Thr) c.443G>C (p.Ser148Thr) | |
| 13 | g.42606569G>T | CA388221055 | TNFSF11 | c.605G>T (p.Ser202Ile) c.464G>T (p.Ser155Ile) c.386G>T (p.Ser129Ile) c.443G>T (p.Ser148Ile) | |
| 13 | g.42606570C>A | CA388221060 | TNFSF11 | c.606C>A (p.Ser202Arg) c.465C>A (p.Ser155Arg) c.387C>A (p.Ser129Arg) c.444C>A (p.Ser148Arg) | |
| 13 | g.42606570C= | CA2087395066 | TNFSF11 | c.606C= (p.Ser202=) c.465C= (p.Ser155=) c.387C= (p.Ser129=) c.444C= (p.Ser148=) | |
| 13 | g.42606570C>G | CA388221061 | TNFSF11 | c.606C>G (p.Ser202Arg) c.465C>G (p.Ser155Arg) c.387C>G (p.Ser129Arg) c.444C>G (p.Ser148Arg) | |
| 13 | g.42606570C>T | CA483605019 | TNFSF11 | c.606C>T (p.Ser202=) c.465C>T (p.Ser155=) c.387C>T (p.Ser129=) c.444C>T (p.Ser148=) | ClinVar dbSNP gnomAD v4 |
| 13 | g.42606571A>C | CA388221069 | TNFSF11 | c.607A>C (p.Asn203His) c.466A>C (p.Asn156His) c.388A>C (p.Asn130His) c.445A>C (p.Asn149His) | gnomAD v4 |
| 13 | g.42606571A>G | CA388221071 | TNFSF11 | c.607A>G (p.Asn203Asp) c.466A>G (p.Asn156Asp) c.388A>G (p.Asn130Asp) c.445A>G (p.Asn149Asp) | |
| 13 | g.42606571A>T | CA388221072 | TNFSF11 | c.607A>T (p.Asn203Tyr) c.466A>T (p.Asn156Tyr) c.388A>T (p.Asn130Tyr) c.445A>T (p.Asn149Tyr) | |
| 13 | g.42606572A= | CA2087395067 | TNFSF11 | c.608A= (p.Asn203=) c.467A= (p.Asn156=) c.389A= (p.Asn130=) c.446A= (p.Asn149=) | |
| 13 | g.42606572A>C | CA388221075 | TNFSF11 | c.608A>C (p.Asn203Thr) c.467A>C (p.Asn156Thr) c.389A>C (p.Asn130Thr) c.446A>C (p.Asn149Thr) | |
| 13 | g.42606572A>G | CA6967276 | TNFSF11 | c.608A>G (p.Asn203Ser) c.467A>G (p.Asn156Ser) c.389A>G (p.Asn130Ser) c.446A>G (p.Asn149Ser) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.42606572A>T | CA388221077 | TNFSF11 | c.608A>T (p.Asn203Ile) c.467A>T (p.Asn156Ile) c.389A>T (p.Asn130Ile) c.446A>T (p.Asn149Ile) | |
| 13 | g.42606573T>A | CA388221080 | TNFSF11 | c.609T>A (p.Asn203Lys) c.468T>A (p.Asn156Lys) c.390T>A (p.Asn130Lys) c.447T>A (p.Asn149Lys) | |
| 13 | g.42606573T>C | CA483605020 | TNFSF11 | c.609T>C (p.Asn203=) c.468T>C (p.Asn156=) c.390T>C (p.Asn130=) c.447T>C (p.Asn149=) | |
| 13 | g.42606573T>G | CA388221082 | TNFSF11 | c.609T>G (p.Asn203Lys) c.468T>G (p.Asn156Lys) c.390T>G (p.Asn130Lys) c.447T>G (p.Asn149Lys) | |
| 13 | g.42606574G>A | CA388221085 | TNFSF11 | c.610G>A (p.Gly204Arg) c.469G>A (p.Gly157Arg) c.391G>A (p.Gly131Arg) c.448G>A (p.Gly150Arg) | |
| 13 | g.42606574G>C | CA388221086 | TNFSF11 | c.610G>C (p.Gly204Arg) c.469G>C (p.Gly157Arg) c.391G>C (p.Gly131Arg) c.448G>C (p.Gly150Arg) | |
| 13 | g.42606574G>T | CA388221088 | TNFSF11 | c.610G>T (p.Gly204Ter) c.469G>T (p.Gly157Ter) c.391G>T (p.Gly131Ter) c.448G>T (p.Gly150Ter) | COSMIC |
| 13 | g.42606575G>A | CA388221091 | TNFSF11 | c.611G>A (p.Gly204Glu) c.470G>A (p.Gly157Glu) c.392G>A (p.Gly131Glu) c.449G>A (p.Gly150Glu) | COSMIC |
| 13 | g.42606575G>C | CA388221097 | TNFSF11 | c.611G>C (p.Gly204Ala) c.470G>C (p.Gly157Ala) c.392G>C (p.Gly131Ala) c.449G>C (p.Gly150Ala) | |
| 13 | g.42606575G>T | CA388221092 | TNFSF11 | c.611G>T (p.Gly204Val) c.470G>T (p.Gly157Val) c.392G>T (p.Gly131Val) c.449G>T (p.Gly150Val) | |
| 13 | g.42606576A>C | CA483605021 | TNFSF11 | c.612A>C (p.Gly204=) c.471A>C (p.Gly157=) c.393A>C (p.Gly131=) c.450A>C (p.Gly150=) | |
| 13 | g.42606576A>G | CA483605022 | TNFSF11 | c.612A>G (p.Gly204=) c.471A>G (p.Gly157=) c.393A>G (p.Gly131=) c.450A>G (p.Gly150=) | gnomAD v4 |
| 13 | g.42606576A>T | CA483605023 | TNFSF11 | c.612A>T (p.Gly204=) c.471A>T (p.Gly157=) c.393A>T (p.Gly131=) c.450A>T (p.Gly150=) | |
| 13 | g.42606577A>C | CA388221102 | TNFSF11 | c.613A>C (p.Lys205Gln) c.472A>C (p.Lys158Gln) c.394A>C (p.Lys132Gln) c.451A>C (p.Lys151Gln) | |
| 13 | g.42606577A>G | CA388221104 | TNFSF11 | c.613A>G (p.Lys205Glu) c.472A>G (p.Lys158Glu) c.394A>G (p.Lys132Glu) c.451A>G (p.Lys151Glu) | |
| 13 | g.42606577A>T | CA388221106 | TNFSF11 | c.613A>T (p.Lys205Ter) c.472A>T (p.Lys158Ter) c.394A>T (p.Lys132Ter) c.451A>T (p.Lys151Ter) | |
| 13 | g.42606578A>C | CA388221107 | TNFSF11 | c.614A>C (p.Lys205Thr) c.473A>C (p.Lys158Thr) c.395A>C (p.Lys132Thr) c.452A>C (p.Lys151Thr) | |
| 13 | g.42606578A>G | CA388221108 | TNFSF11 | c.614A>G (p.Lys205Arg) c.473A>G (p.Lys158Arg) c.395A>G (p.Lys132Arg) c.452A>G (p.Lys151Arg) | |
| 13 | g.42606578A>T | CA388221109 | TNFSF11 | c.614A>T (p.Lys205Ile) c.473A>T (p.Lys158Ile) c.395A>T (p.Lys132Ile) c.452A>T (p.Lys151Ile) | |
| 13 | g.42606579A>C | CA388221111 | TNFSF11 | c.615A>C (p.Lys205Asn) c.474A>C (p.Lys158Asn) c.396A>C (p.Lys132Asn) c.453A>C (p.Lys151Asn) | |
| 13 | g.42606579A>G | CA483605024 | TNFSF11 | c.615A>G (p.Lys205=) c.474A>G (p.Lys158=) c.396A>G (p.Lys132=) c.453A>G (p.Lys151=) | |
| 13 | g.42606579A>T | CA388221113 | TNFSF11 | c.615A>T (p.Lys205Asn) c.474A>T (p.Lys158Asn) c.396A>T (p.Lys132Asn) c.453A>T (p.Lys151Asn) | |
| 13 | g.42606580C>A | CA388221116 | TNFSF11 | c.616C>A (p.Leu206Ile) c.475C>A (p.Leu159Ile) c.397C>A (p.Leu133Ile) c.454C>A (p.Leu152Ile) | |
| 13 | g.42606580C>G | CA388221118 | TNFSF11 | c.616C>G (p.Leu206Val) c.475C>G (p.Leu159Val) c.397C>G (p.Leu133Val) c.454C>G (p.Leu152Val) | |
| 13 | g.42606580C>T | CA483605025 | TNFSF11 | c.616C>T (p.Leu206=) c.475C>T (p.Leu159=) c.397C>T (p.Leu133=) c.454C>T (p.Leu152=) | |
| 13 | g.42606581T>A | CA388221124 | TNFSF11 | c.617T>A (p.Leu206Gln) c.476T>A (p.Leu159Gln) c.398T>A (p.Leu133Gln) c.455T>A (p.Leu152Gln) | |
| 13 | g.42606581T>C | CA388221122 | TNFSF11 | c.617T>C (p.Leu206Pro) c.476T>C (p.Leu159Pro) c.398T>C (p.Leu133Pro) c.455T>C (p.Leu152Pro) | |
| 13 | g.42606581T>G | CA388221119 | TNFSF11 | c.617T>G (p.Leu206Arg) c.476T>G (p.Leu159Arg) c.398T>G (p.Leu133Arg) c.455T>G (p.Leu152Arg) | |
| 13 | g.42606582A= | CA2087395068 | TNFSF11 | c.618A= (p.Leu206=) c.477A= (p.Leu159=) c.399A= (p.Leu133=) c.456A= (p.Leu152=) | |
| 13 | g.42606582A>C | CA483605026 | TNFSF11 | c.618A>C (p.Leu206=) c.477A>C (p.Leu159=) c.399A>C (p.Leu133=) c.456A>C (p.Leu152=) | |
| 13 | g.42606582A>G | CA6967277 | TNFSF11 | c.618A>G (p.Leu206=) c.477A>G (p.Leu159=) c.399A>G (p.Leu133=) c.456A>G (p.Leu152=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 13 | g.42606582A>T | CA483605027 | TNFSF11 | c.618A>T (p.Leu206=) c.477A>T (p.Leu159=) c.399A>T (p.Leu133=) c.456A>T (p.Leu152=) | |
| 13 | g.42606583del | CA2622837736 | TNFSF11 | c.619del (p.Ile207Ter) c.478del (p.Ile160Ter) c.400del (p.Ile134Ter) c.457del (p.Ile153Ter) | gnomAD v4 |
| 13 | g.42606583A= | CA2087395069 | TNFSF11 | c.619A= (p.Ile207=) c.478A= (p.Ile160=) c.400A= (p.Ile134=) c.457A= (p.Ile153=) | |
| 13 | g.42606583A>C | CA388221129 | TNFSF11 | c.619A>C (p.Ile207Leu) c.478A>C (p.Ile160Leu) c.400A>C (p.Ile134Leu) c.457A>C (p.Ile153Leu) | |
| 13 | g.42606583A>G | CA388221132 | TNFSF11 | c.619A>G (p.Ile207Val) c.478A>G (p.Ile160Val) c.400A>G (p.Ile134Val) c.457A>G (p.Ile153Val) | dbSNP gnomAD v2 gnomAD v4 |
| 13 | g.42606583A>T | CA388221134 | TNFSF11 | c.619A>T (p.Ile207Leu) c.478A>T (p.Ile160Leu) c.400A>T (p.Ile134Leu) c.457A>T (p.Ile153Leu) | |
| 13 | g.42606584T>A | CA388221136 | TNFSF11 | c.620T>A (p.Ile207Lys) c.479T>A (p.Ile160Lys) c.401T>A (p.Ile134Lys) c.458T>A (p.Ile153Lys) | |
| 13 | g.42606584T>C | CA249053398 | TNFSF11 | c.620T>C (p.Ile207Thr) c.479T>C (p.Ile160Thr) c.401T>C (p.Ile134Thr) c.458T>C (p.Ile153Thr) | ClinVar dbSNP gnomAD v4 |
| 13 | g.42606584T>G | CA388221140 | TNFSF11 | c.620T>G (p.Ile207Arg) c.479T>G (p.Ile160Arg) c.401T>G (p.Ile134Arg) c.458T>G (p.Ile153Arg) | |
| 13 | g.42606584T= | CA2087395070 | TNFSF11 | c.620T= (p.Ile207=) c.479T= (p.Ile160=) c.401T= (p.Ile134=) c.458T= (p.Ile153=) | |
| 13 | g.42606585A= | CA2087395071 | TNFSF11 | c.621A= (p.Ile207=) c.480A= (p.Ile160=) c.402A= (p.Ile134=) c.459A= (p.Ile153=) | |
| 13 | g.42606585A>C | CA483605028 | TNFSF11 | c.621A>C (p.Ile207=) c.480A>C (p.Ile160=) c.402A>C (p.Ile134=) c.459A>C (p.Ile153=) | |
| 13 | g.42606585A>G | CA6967278 | TNFSF11 | c.621A>G (p.Ile207Met) c.480A>G (p.Ile160Met) c.402A>G (p.Ile134Met) c.459A>G (p.Ile153Met) | dbSNP ExAC gnomAD v2 |
| 13 | g.42606585A>T | CA483605029 | TNFSF11 | c.621A>T (p.Ile207=) c.480A>T (p.Ile160=) c.402A>T (p.Ile134=) c.459A>T (p.Ile153=) | |
| 13 | g.42606586G>A | CA388221143 | TNFSF11 | c.622G>A (p.Val208Ile) c.481G>A (p.Val161Ile) c.403G>A (p.Val135Ile) c.460G>A (p.Val154Ile) | gnomAD v4 |
| 13 | g.42606586G>C | CA388221145 | TNFSF11 | c.622G>C (p.Val208Leu) c.481G>C (p.Val161Leu) c.403G>C (p.Val135Leu) c.460G>C (p.Val154Leu) | |
| 13 | g.42606586G>T | CA388221147 | TNFSF11 | c.622G>T (p.Val208Phe) c.481G>T (p.Val161Phe) c.403G>T (p.Val135Phe) c.460G>T (p.Val154Phe) | |
| 13 | g.42606587T>A | CA388221150 | TNFSF11 | c.623T>A (p.Val208Asp) c.482T>A (p.Val161Asp) c.404T>A (p.Val135Asp) c.461T>A (p.Val154Asp) | |
| 13 | g.42606587T>C | CA388221152 | TNFSF11 | c.623T>C (p.Val208Ala) c.482T>C (p.Val161Ala) c.404T>C (p.Val135Ala) c.461T>C (p.Val154Ala) | gnomAD v4 |
| 13 | g.42606587T>G | CA388221155 | TNFSF11 | c.623T>G (p.Val208Gly) c.482T>G (p.Val161Gly) c.404T>G (p.Val135Gly) c.461T>G (p.Val154Gly) | |
| 13 | g.42606588T>A | CA483605030 | TNFSF11 | c.624T>A (p.Val208=) c.483T>A (p.Val161=) c.405T>A (p.Val135=) c.462T>A (p.Val154=) | |
| 13 | g.42606588T>C | CA483605031 | TNFSF11 | c.624T>C (p.Val208=) c.483T>C (p.Val161=) c.405T>C (p.Val135=) c.462T>C (p.Val154=) | |
| 13 | g.42606588T>G | CA483605032 | TNFSF11 | c.624T>G (p.Val208=) c.483T>G (p.Val161=) c.405T>G (p.Val135=) c.462T>G (p.Val154=) | |
| 13 | g.42606589A>C | CA388221157 | TNFSF11 | c.625A>C (p.Asn209His) c.484A>C (p.Asn162His) c.406A>C (p.Asn136His) c.463A>C (p.Asn155His) | |
| 13 | g.42606589A>G | CA388221161 | TNFSF11 | c.625A>G (p.Asn209Asp) c.484A>G (p.Asn162Asp) c.406A>G (p.Asn136Asp) c.463A>G (p.Asn155Asp) | |
| 13 | g.42606589A>T | CA388221159 | TNFSF11 | c.625A>T (p.Asn209Tyr) c.484A>T (p.Asn162Tyr) c.406A>T (p.Asn136Tyr) c.463A>T (p.Asn155Tyr) | |
| 13 | g.42606590A>C | CA388221164 | TNFSF11 | c.626A>C (p.Asn209Thr) c.485A>C (p.Asn162Thr) c.407A>C (p.Asn136Thr) c.464A>C (p.Asn155Thr) | |
| 13 | g.42606590A>G | CA388221165 | TNFSF11 | c.626A>G (p.Asn209Ser) c.485A>G (p.Asn162Ser) c.407A>G (p.Asn136Ser) c.464A>G (p.Asn155Ser) | |
| 13 | g.42606590A>T | CA388221168 | TNFSF11 | c.626A>T (p.Asn209Ile) c.485A>T (p.Asn162Ile) c.407A>T (p.Asn136Ile) c.464A>T (p.Asn155Ile) | |
| 13 | g.42606591T>A | CA388221170 | TNFSF11 | c.627T>A (p.Asn209Lys) c.486T>A (p.Asn162Lys) c.408T>A (p.Asn136Lys) c.465T>A (p.Asn155Lys) | |
| 13 | g.42606591T>C | CA483605033 | TNFSF11 | c.627T>C (p.Asn209=) c.486T>C (p.Asn162=) c.408T>C (p.Asn136=) c.465T>C (p.Asn155=) | dbSNP |
| 13 | g.42606591T>G | CA388221172 | TNFSF11 | c.627T>G (p.Asn209Lys) c.486T>G (p.Asn162Lys) c.408T>G (p.Asn136Lys) c.465T>G (p.Asn155Lys) | |
| 13 | g.42606591T= | CA2087395072 | TNFSF11 | c.627T= (p.Asn209=) c.486T= (p.Asn162=) c.408T= (p.Asn136=) c.465T= (p.Asn155=) | |
| 13 | g.42606592C>A | CA388221175 | TNFSF11 | c.628C>A (p.Gln210Lys) c.487C>A (p.Gln163Lys) c.409C>A (p.Gln137Lys) c.466C>A (p.Gln156Lys) | |
| 13 | g.42606592C>G | CA388221176 | TNFSF11 | c.628C>G (p.Gln210Glu) c.487C>G (p.Gln163Glu) c.409C>G (p.Gln137Glu) c.466C>G (p.Gln156Glu) | |
| 13 | g.42606592C>T | CA388221179 | TNFSF11 | c.628C>T (p.Gln210Ter) c.487C>T (p.Gln163Ter) c.409C>T (p.Gln137Ter) c.466C>T (p.Gln156Ter) | |
| 13 | g.42606593A>C | CA388221181 | TNFSF11 | c.629A>C (p.Gln210Pro) c.488A>C (p.Gln163Pro) c.410A>C (p.Gln137Pro) c.467A>C (p.Gln156Pro) | |
| 13 | g.42606593A>G | CA388221182 | TNFSF11 | c.629A>G (p.Gln210Arg) c.488A>G (p.Gln163Arg) c.410A>G (p.Gln137Arg) c.467A>G (p.Gln156Arg) | |
| 13 | g.42606593A>T | CA388221184 | TNFSF11 | c.629A>T (p.Gln210Leu) c.488A>T (p.Gln163Leu) c.410A>T (p.Gln137Leu) c.467A>T (p.Gln156Leu) | |
| 13 | g.42606594G>A | CA483605034 | TNFSF11 | c.630G>A (p.Gln210=) c.489G>A (p.Gln163=) c.411G>A (p.Gln137=) c.468G>A (p.Gln156=) | |
| 13 | g.42606594G>C | CA388221187 | TNFSF11 | c.630G>C (p.Gln210His) c.489G>C (p.Gln163His) c.411G>C (p.Gln137His) c.468G>C (p.Gln156His) | |
| 13 | g.42606594G>T | CA388221188 | TNFSF11 | c.630G>T (p.Gln210His) c.489G>T (p.Gln163His) c.411G>T (p.Gln137His) c.468G>T (p.Gln156His) | |
| 13 | g.42606595G>A | CA388221191 | TNFSF11 | c.631G>A (p.Asp211Asn) c.490G>A (p.Asp164Asn) c.412G>A (p.Asp138Asn) c.469G>A (p.Asp157Asn) | |
| 13 | g.42606595G>C | CA388221193 | TNFSF11 | c.631G>C (p.Asp211His) c.490G>C (p.Asp164His) c.412G>C (p.Asp138His) c.469G>C (p.Asp157His) | |
| 13 | g.42606595G>T | CA388221196 | TNFSF11 | c.631G>T (p.Asp211Tyr) c.490G>T (p.Asp164Tyr) c.412G>T (p.Asp138Tyr) c.469G>T (p.Asp157Tyr) | |
| 13 | g.42606596A>C | CA388221198 | TNFSF11 | c.632A>C (p.Asp211Ala) c.491A>C (p.Asp164Ala) c.413A>C (p.Asp138Ala) c.470A>C (p.Asp157Ala) | |
| 13 | g.42606596A>G | CA388221200 | TNFSF11 | c.632A>G (p.Asp211Gly) c.491A>G (p.Asp164Gly) c.413A>G (p.Asp138Gly) c.470A>G (p.Asp157Gly) | ClinVar gnomAD v4 |
| 13 | g.42606596A>T | CA388221202 | TNFSF11 | c.632A>T (p.Asp211Val) c.491A>T (p.Asp164Val) c.413A>T (p.Asp138Val) c.470A>T (p.Asp157Val) | |
| 13 | g.42606597T>A | CA388221207 | TNFSF11 | c.633T>A (p.Asp211Glu) c.492T>A (p.Asp164Glu) c.414T>A (p.Asp138Glu) c.471T>A (p.Asp157Glu) | |
| 13 | g.42606597T>C | CA483605035 | TNFSF11 | c.633T>C (p.Asp211=) c.492T>C (p.Asp164=) c.414T>C (p.Asp138=) c.471T>C (p.Asp157=) | |
| 13 | g.42606597T>G | CA388221205 | TNFSF11 | c.633T>G (p.Asp211Glu) c.492T>G (p.Asp164Glu) c.414T>G (p.Asp138Glu) c.471T>G (p.Asp157Glu) | |
| 13 | g.42606598G>A | CA388221209 | TNFSF11 | c.634G>A (p.Gly212Ser) c.493G>A (p.Gly165Ser) c.415G>A (p.Gly139Ser) c.472G>A (p.Gly158Ser) | |
| 13 | g.42606598G>C | CA388221211 | TNFSF11 | c.634G>C (p.Gly212Arg) c.493G>C (p.Gly165Arg) c.415G>C (p.Gly139Arg) c.472G>C (p.Gly158Arg) | |
| 13 | g.42606598G>T | CA388221213 | TNFSF11 | c.634G>T (p.Gly212Cys) c.493G>T (p.Gly165Cys) c.415G>T (p.Gly139Cys) c.472G>T (p.Gly158Cys) | |
| 13 | g.42606599G>A | CA388221216 | TNFSF11 | c.635G>A (p.Gly212Asp) c.494G>A (p.Gly165Asp) c.416G>A (p.Gly139Asp) c.473G>A (p.Gly158Asp) | |
| 13 | g.42606599G>C | CA388221217 | TNFSF11 | c.635G>C (p.Gly212Ala) c.494G>C (p.Gly165Ala) c.416G>C (p.Gly139Ala) c.473G>C (p.Gly158Ala) | |
| 13 | g.42606599G>T | CA388221220 | TNFSF11 | c.635G>T (p.Gly212Val) c.494G>T (p.Gly165Val) c.416G>T (p.Gly139Val) c.473G>T (p.Gly158Val) | |
| 13 | g.42606600C>A | CA483605036 | TNFSF11 | c.636C>A (p.Gly212=) c.495C>A (p.Gly165=) c.417C>A (p.Gly139=) c.474C>A (p.Gly158=) | gnomAD v4 COSMIC |
| 13 | g.42606600C= | CA2087395073 | TNFSF11 | c.636C= (p.Gly212=) c.495C= (p.Gly165=) c.417C= (p.Gly139=) c.474C= (p.Gly158=) | |
| 13 | g.42606600C>G | CA483605037 | TNFSF11 | c.636C>G (p.Gly212=) c.495C>G (p.Gly165=) c.417C>G (p.Gly139=) c.474C>G (p.Gly158=) | dbSNP |
| 13 | g.42606600C>T | CA483605038 | TNFSF11 | c.636C>T (p.Gly212=) c.495C>T (p.Gly165=) c.417C>T (p.Gly139=) c.474C>T (p.Gly158=) | |
| 13 | g.42606601T>A | CA388221226 | TNFSF11 | c.637T>A (p.Phe213Ile) c.496T>A (p.Phe166Ile) c.418T>A (p.Phe140Ile) c.475T>A (p.Phe159Ile) | |
| 13 | g.42606601T>C | CA388221222 | TNFSF11 | c.637T>C (p.Phe213Leu) c.496T>C (p.Phe166Leu) c.418T>C (p.Phe140Leu) c.475T>C (p.Phe159Leu) | |
| 13 | g.42606601T>G | CA388221224 | TNFSF11 | c.637T>G (p.Phe213Val) c.496T>G (p.Phe166Val) c.418T>G (p.Phe140Val) c.475T>G (p.Phe159Val) | |
| 13 | g.42606602T>A | CA388221229 | TNFSF11 | c.638T>A (p.Phe213Tyr) c.497T>A (p.Phe166Tyr) c.419T>A (p.Phe140Tyr) c.476T>A (p.Phe159Tyr) | |
| 13 | g.42606602T>C | CA388221231 | TNFSF11 | c.638T>C (p.Phe213Ser) c.497T>C (p.Phe166Ser) c.419T>C (p.Phe140Ser) c.476T>C (p.Phe159Ser) | |
| 13 | g.42606602T>G | CA388221232 | TNFSF11 | c.638T>G (p.Phe213Cys) c.497T>G (p.Phe166Cys) c.419T>G (p.Phe140Cys) c.476T>G (p.Phe159Cys) | |
| 13 | g.42606603T>A | CA388221234 | TNFSF11 | c.639T>A (p.Phe213Leu) c.498T>A (p.Phe166Leu) c.420T>A (p.Phe140Leu) c.477T>A (p.Phe159Leu) | |
| 13 | g.42606603T>C | CA483605039 | TNFSF11 | c.639T>C (p.Phe213=) c.498T>C (p.Phe166=) c.420T>C (p.Phe140=) c.477T>C (p.Phe159=) | dbSNP gnomAD v4 |
| 13 | g.42606603T>G | CA388221236 | TNFSF11 | c.639T>G (p.Phe213Leu) c.498T>G (p.Phe166Leu) c.420T>G (p.Phe140Leu) c.477T>G (p.Phe159Leu) | gnomAD v4 |
| 13 | g.42606603T= | CA2087395074 | TNFSF11 | c.639T= (p.Phe213=) c.498T= (p.Phe166=) c.420T= (p.Phe140=) c.477T= (p.Phe159=) | |
| 13 | g.42606604T>A | CA388221238 | TNFSF11 | c.640T>A (p.Tyr214Asn) c.499T>A (p.Tyr167Asn) c.421T>A (p.Tyr141Asn) c.478T>A (p.Tyr160Asn) | |
| 13 | g.42606604T>C | CA388221239 | TNFSF11 | c.640T>C (p.Tyr214His) c.499T>C (p.Tyr167His) c.421T>C (p.Tyr141His) c.478T>C (p.Tyr160His) | |
| 13 | g.42606604T>G | CA388221241 | TNFSF11 | c.640T>G (p.Tyr214Asp) c.499T>G (p.Tyr167Asp) c.421T>G (p.Tyr141Asp) c.478T>G (p.Tyr160Asp) | |
| 13 | g.42606605A>C | CA388221243 | TNFSF11 | c.641A>C (p.Tyr214Ser) c.500A>C (p.Tyr167Ser) c.422A>C (p.Tyr141Ser) c.479A>C (p.Tyr160Ser) | |
| 13 | g.42606605A>G | CA388221245 | TNFSF11 | c.641A>G (p.Tyr214Cys) c.500A>G (p.Tyr167Cys) c.422A>G (p.Tyr141Cys) c.479A>G (p.Tyr160Cys) | |
| 13 | g.42606605A>T | CA388221247 | TNFSF11 | c.641A>T (p.Tyr214Phe) c.500A>T (p.Tyr167Phe) c.422A>T (p.Tyr141Phe) c.479A>T (p.Tyr160Phe) | |
| 13 | g.42606606T>A | CA388221249 | TNFSF11 | c.642T>A (p.Tyr214Ter) c.501T>A (p.Tyr167Ter) c.423T>A (p.Tyr141Ter) c.480T>A (p.Tyr160Ter) | |
| 13 | g.42606606T>C | CA483605041 | TNFSF11 | c.642T>C (p.Tyr214=) c.501T>C (p.Tyr167=) c.423T>C (p.Tyr141=) c.480T>C (p.Tyr160=) | |
| 13 | g.42606606T>G | CA388221251 | TNFSF11 | c.642T>G (p.Tyr214Ter) c.501T>G (p.Tyr167Ter) c.423T>G (p.Tyr141Ter) c.480T>G (p.Tyr160Ter) | |
| 13 | g.42606607T>A | CA388221253 | TNFSF11 | c.643T>A (p.Tyr215Asn) c.502T>A (p.Tyr168Asn) c.424T>A (p.Tyr142Asn) c.481T>A (p.Tyr161Asn) | |
| 13 | g.42606607T>C | CA388221258 | TNFSF11 | c.643T>C (p.Tyr215His) c.502T>C (p.Tyr168His) c.424T>C (p.Tyr142His) c.481T>C (p.Tyr161His) | |
| 13 | g.42606607T>G | CA388221256 | TNFSF11 | c.643T>G (p.Tyr215Asp) c.502T>G (p.Tyr168Asp) c.424T>G (p.Tyr142Asp) c.481T>G (p.Tyr161Asp) | |
| 13 | g.42606608A>C | CA388221260 | TNFSF11 | c.644A>C (p.Tyr215Ser) c.503A>C (p.Tyr168Ser) c.425A>C (p.Tyr142Ser) c.482A>C (p.Tyr161Ser) | |
| 13 | g.42606608A>G | CA388221261 | TNFSF11 | c.644A>G (p.Tyr215Cys) c.503A>G (p.Tyr168Cys) c.425A>G (p.Tyr142Cys) c.482A>G (p.Tyr161Cys) | |
| 13 | g.42606608A>T | CA388221263 | TNFSF11 | c.644A>T (p.Tyr215Phe) c.503A>T (p.Tyr168Phe) c.425A>T (p.Tyr142Phe) c.482A>T (p.Tyr161Phe) | |
| 13 | g.42606609C>A | CA388221264 | TNFSF11 | c.645C>A (p.Tyr215Ter) c.504C>A (p.Tyr168Ter) c.426C>A (p.Tyr142Ter) c.483C>A (p.Tyr161Ter) | |
| 13 | g.42606609C= | CA2087395075 | TNFSF11 | c.645C= (p.Tyr215=) c.504C= (p.Tyr168=) c.426C= (p.Tyr142=) c.483C= (p.Tyr161=) | |
| 13 | g.42606609C>G | CA6967279 | TNFSF11 | c.645C>G (p.Tyr215Ter) c.504C>G (p.Tyr168Ter) c.426C>G (p.Tyr142Ter) c.483C>G (p.Tyr161Ter) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.42606609C>T | CA483605042 | TNFSF11 | c.645C>T (p.Tyr215=) c.504C>T (p.Tyr168=) c.426C>T (p.Tyr142=) c.483C>T (p.Tyr161=) | dbSNP |
| 13 | g.42606610C>A | CA388221266 | TNFSF11 | c.646C>A (p.Leu216Met) c.505C>A (p.Leu169Met) c.427C>A (p.Leu143Met) c.484C>A (p.Leu162Met) | |
| 13 | g.42606610C>G | CA388221268 | TNFSF11 | c.646C>G (p.Leu216Val) c.505C>G (p.Leu169Val) c.427C>G (p.Leu143Val) c.484C>G (p.Leu162Val) | |
| 13 | g.42606610C>T | CA483605044 | TNFSF11 | c.646C>T (p.Leu216=) c.505C>T (p.Leu169=) c.427C>T (p.Leu143=) c.484C>T (p.Leu162=) | COSMIC |
| 13 | g.42606611T>A | CA388221271 | TNFSF11 | c.647T>A (p.Leu216Gln) c.506T>A (p.Leu169Gln) c.428T>A (p.Leu143Gln) c.485T>A (p.Leu162Gln) | |
| 13 | g.42606611T>C | CA388221272 | TNFSF11 | c.647T>C (p.Leu216Pro) c.506T>C (p.Leu169Pro) c.428T>C (p.Leu143Pro) c.485T>C (p.Leu162Pro) | |
| 13 | g.42606611T>G | CA388221274 | TNFSF11 | c.647T>G (p.Leu216Arg) c.506T>G (p.Leu169Arg) c.428T>G (p.Leu143Arg) c.485T>G (p.Leu162Arg) | |
| 13 | g.42606612G>A | CA483605045 | TNFSF11 | c.648G>A (p.Leu216=) c.507G>A (p.Leu169=) c.429G>A (p.Leu143=) c.486G>A (p.Leu162=) | |
| 13 | g.42606612G>C | CA483605046 | TNFSF11 | c.648G>C (p.Leu216=) c.507G>C (p.Leu169=) c.429G>C (p.Leu143=) c.486G>C (p.Leu162=) | gnomAD v4 |
| 13 | g.42606612G>T | CA483605047 | TNFSF11 | c.648G>T (p.Leu216=) c.507G>T (p.Leu169=) c.429G>T (p.Leu143=) c.486G>T (p.Leu162=) | |
| 13 | g.42606613T>A | CA388221277 | TNFSF11 | c.649T>A (p.Tyr217Asn) c.508T>A (p.Tyr170Asn) c.430T>A (p.Tyr144Asn) c.487T>A (p.Tyr163Asn) | |
| 13 | g.42606613T>C | CA388221278 | TNFSF11 | c.649T>C (p.Tyr217His) c.508T>C (p.Tyr170His) c.430T>C (p.Tyr144His) c.487T>C (p.Tyr163His) | gnomAD v4 |
| 13 | g.42606613T>G | CA388221281 | TNFSF11 | c.649T>G (p.Tyr217Asp) c.508T>G (p.Tyr170Asp) c.430T>G (p.Tyr144Asp) c.487T>G (p.Tyr163Asp) | |
| 13 | g.42606614A>C | CA388221287 | TNFSF11 | c.650A>C (p.Tyr217Ser) c.509A>C (p.Tyr170Ser) c.431A>C (p.Tyr144Ser) c.488A>C (p.Tyr163Ser) | |
| 13 | g.42606614A>G | CA388221283 | TNFSF11 | c.650A>G (p.Tyr217Cys) c.509A>G (p.Tyr170Cys) c.431A>G (p.Tyr144Cys) c.488A>G (p.Tyr163Cys) | gnomAD v4 |
| 13 | g.42606614A>T | CA388221285 | TNFSF11 | c.650A>T (p.Tyr217Phe) c.509A>T (p.Tyr170Phe) c.431A>T (p.Tyr144Phe) c.488A>T (p.Tyr163Phe) | |
| 13 | g.42606615T>A | CA388221289 | TNFSF11 | c.651T>A (p.Tyr217Ter) c.510T>A (p.Tyr170Ter) c.432T>A (p.Tyr144Ter) c.489T>A (p.Tyr163Ter) | |
| 13 | g.42606615T>C | CA483605048 | TNFSF11 | c.651T>C (p.Tyr217=) c.510T>C (p.Tyr170=) c.432T>C (p.Tyr144=) c.489T>C (p.Tyr163=) | |
| 13 | g.42606615T>G | CA388221291 | TNFSF11 | c.651T>G (p.Tyr217Ter) c.510T>G (p.Tyr170Ter) c.432T>G (p.Tyr144Ter) c.489T>G (p.Tyr163Ter) | |
| 13 | g.42606616G>A | CA388221293 | TNFSF11 | c.652G>A (p.Ala218Thr) c.511G>A (p.Ala171Thr) c.433G>A (p.Ala145Thr) c.490G>A (p.Ala164Thr) | |
| 13 | g.42606616G>C | CA388221295 | TNFSF11 | c.652G>C (p.Ala218Pro) c.511G>C (p.Ala171Pro) c.433G>C (p.Ala145Pro) c.490G>C (p.Ala164Pro) | |
| 13 | g.42606616G>T | CA388221297 | TNFSF11 | c.652G>T (p.Ala218Ser) c.511G>T (p.Ala171Ser) c.433G>T (p.Ala145Ser) c.490G>T (p.Ala164Ser) | |
| 13 | g.42606617C>A | CA388221300 | TNFSF11 | c.653C>A (p.Ala218Asp) c.512C>A (p.Ala171Asp) c.434C>A (p.Ala145Asp) c.491C>A (p.Ala164Asp) | |
| 13 | g.42606617C>G | CA388221301 | TNFSF11 | c.653C>G (p.Ala218Gly) c.512C>G (p.Ala171Gly) c.434C>G (p.Ala145Gly) c.491C>G (p.Ala164Gly) | |
| 13 | g.42606617C>T | CA388221302 | TNFSF11 | c.653C>T (p.Ala218Val) c.512C>T (p.Ala171Val) c.434C>T (p.Ala145Val) c.491C>T (p.Ala164Val) | |
| 13 | g.42606618C>A | CA483605049 | TNFSF11 | c.654C>A (p.Ala218=) c.513C>A (p.Ala171=) c.435C>A (p.Ala145=) c.492C>A (p.Ala164=) | |
| 13 | g.42606618C>G | CA483605050 | TNFSF11 | c.654C>G (p.Ala218=) c.513C>G (p.Ala171=) c.435C>G (p.Ala145=) c.492C>G (p.Ala164=) | |
| 13 | g.42606618C>T | CA483605051 | TNFSF11 | c.654C>T (p.Ala218=) c.513C>T (p.Ala171=) c.435C>T (p.Ala145=) c.492C>T (p.Ala164=) | |
| 13 | g.42606619A>C | CA388221305 | TNFSF11 | c.655A>C (p.Asn219His) c.514A>C (p.Asn172His) c.436A>C (p.Asn146His) c.493A>C (p.Asn165His) | |
| 13 | g.42606619A>G | CA388221307 | TNFSF11 | c.655A>G (p.Asn219Asp) c.514A>G (p.Asn172Asp) c.436A>G (p.Asn146Asp) c.493A>G (p.Asn165Asp) | |
| 13 | g.42606619A>T | CA388221309 | TNFSF11 | c.655A>T (p.Asn219Tyr) c.514A>T (p.Asn172Tyr) c.436A>T (p.Asn146Tyr) c.493A>T (p.Asn165Tyr) | |
| 13 | g.42606620A>C | CA388221312 | TNFSF11 | c.656A>C (p.Asn219Thr) c.515A>C (p.Asn172Thr) c.437A>C (p.Asn146Thr) c.494A>C (p.Asn165Thr) | |
| 13 | g.42606620A>G | CA388221315 | TNFSF11 | c.656A>G (p.Asn219Ser) c.515A>G (p.Asn172Ser) c.437A>G (p.Asn146Ser) c.494A>G (p.Asn165Ser) | gnomAD v4 |
| 13 | g.42606620A>T | CA388221313 | TNFSF11 | c.656A>T (p.Asn219Ile) c.515A>T (p.Asn172Ile) c.437A>T (p.Asn146Ile) c.494A>T (p.Asn165Ile) | |
| 13 | g.42606620_42606621insG | CA645580105 | TNFSF11 | c.656_657insG (p.Asn219LysfsTer8) c.515_516insG (p.Asn172LysfsTer8) c.437_438insG (p.Asn146LysfsTer8) c.494_495insG (p.Asn165LysfsTer8) | COSMIC |
| 13 | g.42606621C>A | CA388221317 | TNFSF11 | c.657C>A (p.Asn219Lys) c.516C>A (p.Asn172Lys) c.438C>A (p.Asn146Lys) c.495C>A (p.Asn165Lys) | |
| 13 | g.42606621C= | CA2087395076 | TNFSF11 | c.657C= (p.Asn219=) c.516C= (p.Asn172=) c.438C= (p.Asn146=) c.495C= (p.Asn165=) | |
| 13 | g.42606621C>G | CA388221319 | TNFSF11 | c.657C>G (p.Asn219Lys) c.516C>G (p.Asn172Lys) c.438C>G (p.Asn146Lys) c.495C>G (p.Asn165Lys) | |
| 13 | g.42606621C>T | CA483605052 | TNFSF11 | c.657C>T (p.Asn219=) c.516C>T (p.Asn172=) c.438C>T (p.Asn146=) c.495C>T (p.Asn165=) | dbSNP |
| 13 | g.42606621_42606622insG | CA483605053 | TNFSF11 | c.657_658insG (p.Ile220AspfsTer7) c.516_517insG (p.Ile173AspfsTer7) c.438_439insG (p.Ile147AspfsTer7) c.495_496insG (p.Ile166AspfsTer7) | COSMIC |
| 13 | g.42606622A= | CA2087395077 | TNFSF11 | c.658A= (p.Ile220=) c.517A= (p.Ile173=) c.439A= (p.Ile147=) c.496A= (p.Ile166=) | |
| 13 | g.42606622A>C | CA388221321 | TNFSF11 | c.658A>C (p.Ile220Leu) c.517A>C (p.Ile173Leu) c.439A>C (p.Ile147Leu) c.496A>C (p.Ile166Leu) | |
| 13 | g.42606622A>G | CA6967280 | TNFSF11 | c.658A>G (p.Ile220Val) c.517A>G (p.Ile173Val) c.439A>G (p.Ile147Val) c.496A>G (p.Ile166Val) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 13 | g.42606622A>T | CA388221323 | TNFSF11 | c.658A>T (p.Ile220Phe) c.517A>T (p.Ile173Phe) c.439A>T (p.Ile147Phe) c.496A>T (p.Ile166Phe) | |
| 13 | g.42606623T>A | CA388221326 | TNFSF11 | c.659T>A (p.Ile220Asn) c.518T>A (p.Ile173Asn) c.440T>A (p.Ile147Asn) c.497T>A (p.Ile166Asn) | |
| 13 | g.42606623T>C | CA388221328 | TNFSF11 | c.659T>C (p.Ile220Thr) c.518T>C (p.Ile173Thr) c.440T>C (p.Ile147Thr) c.497T>C (p.Ile166Thr) | |
| 13 | g.42606623T>G | CA388221330 | TNFSF11 | c.659T>G (p.Ile220Ser) c.518T>G (p.Ile173Ser) c.440T>G (p.Ile147Ser) c.497T>G (p.Ile166Ser) | |
| 13 | g.42606624T>A | CA483605054 | TNFSF11 | c.660T>A (p.Ile220=) c.519T>A (p.Ile173=) c.441T>A (p.Ile147=) c.498T>A (p.Ile166=) | |
| 13 | g.42606624T>C | CA483605055 | TNFSF11 | c.660T>C (p.Ile220=) c.519T>C (p.Ile173=) c.441T>C (p.Ile147=) c.498T>C (p.Ile166=) | |
| 13 | g.42606624T>G | CA388221333 | TNFSF11 | c.660T>G (p.Ile220Met) c.519T>G (p.Ile173Met) c.441T>G (p.Ile147Met) c.498T>G (p.Ile166Met) | dbSNP gnomAD v2 gnomAD v4 |
| 13 | g.42606624T= | CA2087395078 | TNFSF11 | c.660T= (p.Ile220=) c.519T= (p.Ile173=) c.441T= (p.Ile147=) c.498T= (p.Ile166=) | |
| 13 | g.42606625T>A | CA388221339 | TNFSF11 | c.661T>A (p.Cys221Ser) c.520T>A (p.Cys174Ser) c.442T>A (p.Cys148Ser) c.499T>A (p.Cys167Ser) | |
| 13 | g.42606625T>C | CA388221334 | TNFSF11 | c.661T>C (p.Cys221Arg) c.520T>C (p.Cys174Arg) c.442T>C (p.Cys148Arg) c.499T>C (p.Cys167Arg) | |
| 13 | g.42606625T>G | CA388221336 | TNFSF11 | c.661T>G (p.Cys221Gly) c.520T>G (p.Cys174Gly) c.442T>G (p.Cys148Gly) c.499T>G (p.Cys167Gly) | |
| 13 | g.42606626G>A | CA388221341 | TNFSF11 | c.662G>A (p.Cys221Tyr) c.521G>A (p.Cys174Tyr) c.443G>A (p.Cys148Tyr) c.500G>A (p.Cys167Tyr) | |
| 13 | g.42606626G>C | CA388221343 | TNFSF11 | c.662G>C (p.Cys221Ser) c.521G>C (p.Cys174Ser) c.443G>C (p.Cys148Ser) c.500G>C (p.Cys167Ser) | |
| 13 | g.42606626G= | CA2087395079 | TNFSF11 | c.662G= (p.Cys221=) c.521G= (p.Cys174=) c.443G= (p.Cys148=) c.500G= (p.Cys167=) | |
| 13 | g.42606626G>T | CA388221345 | TNFSF11 | c.662G>T (p.Cys221Phe) c.521G>T (p.Cys174Phe) c.443G>T (p.Cys148Phe) c.500G>T (p.Cys167Phe) | dbSNP |
| 13 | g.42606627C>A | CA388221347 | TNFSF11 | c.663C>A (p.Cys221Ter) c.522C>A (p.Cys174Ter) c.444C>A (p.Cys148Ter) c.501C>A (p.Cys167Ter) | |
| 13 | g.42606627C>G | CA388221349 | TNFSF11 | c.663C>G (p.Cys221Trp) c.522C>G (p.Cys174Trp) c.444C>G (p.Cys148Trp) c.501C>G (p.Cys167Trp) | |
| 13 | g.42606627C>T | CA483605056 | TNFSF11 | c.663C>T (p.Cys221=) c.522C>T (p.Cys174=) c.444C>T (p.Cys148=) c.501C>T (p.Cys167=) | ClinVar gnomAD v4 |
| 13 | g.42606628T>A | CA388221356 | TNFSF11 | c.664T>A (p.Phe222Ile) c.523T>A (p.Phe175Ile) c.445T>A (p.Phe149Ile) c.502T>A (p.Phe168Ile) | |
| 13 | g.42606628T>C | CA388221351 | TNFSF11 | c.664T>C (p.Phe222Leu) c.523T>C (p.Phe175Leu) c.445T>C (p.Phe149Leu) c.502T>C (p.Phe168Leu) | |
| 13 | g.42606628T>G | CA388221355 | TNFSF11 | c.664T>G (p.Phe222Val) c.523T>G (p.Phe175Val) c.445T>G (p.Phe149Val) c.502T>G (p.Phe168Val) | |
| 13 | g.42606629T>A | CA388221357 | TNFSF11 | c.665T>A (p.Phe222Tyr) c.524T>A (p.Phe175Tyr) c.446T>A (p.Phe149Tyr) c.503T>A (p.Phe168Tyr) | |
| 13 | g.42606629T>C | CA388221358 | TNFSF11 | c.665T>C (p.Phe222Ser) c.524T>C (p.Phe175Ser) c.446T>C (p.Phe149Ser) c.503T>C (p.Phe168Ser) | |
| 13 | g.42606629T>G | CA388221359 | TNFSF11 | c.665T>G (p.Phe222Cys) c.524T>G (p.Phe175Cys) c.446T>G (p.Phe149Cys) c.503T>G (p.Phe168Cys) | |
| 13 | g.42606630T>A | CA388221360 | TNFSF11 | c.666T>A (p.Phe222Leu) c.525T>A (p.Phe175Leu) c.447T>A (p.Phe149Leu) c.504T>A (p.Phe168Leu) | |
| 13 | g.42606630T>C | CA483605057 | TNFSF11 | c.666T>C (p.Phe222=) c.525T>C (p.Phe175=) c.447T>C (p.Phe149=) c.504T>C (p.Phe168=) | |
| 13 | g.42606630T>G | CA388221361 | TNFSF11 | c.666T>G (p.Phe222Leu) c.525T>G (p.Phe175Leu) c.447T>G (p.Phe149Leu) c.504T>G (p.Phe168Leu) | |
| 13 | g.42606631C>A | CA483605058 | TNFSF11 | c.667C>A (p.Arg223=) c.526C>A (p.Arg176=) c.448C>A (p.Arg150=) c.505C>A (p.Arg169=) | |
| 13 | g.42606631C= | CA2087395080 | TNFSF11 | c.667C= (p.Arg223=) c.526C= (p.Arg176=) c.448C= (p.Arg150=) c.505C= (p.Arg169=) | |
| 13 | g.42606631C>G | CA388221362 | TNFSF11 | c.667C>G (p.Arg223Gly) c.526C>G (p.Arg176Gly) c.448C>G (p.Arg150Gly) c.505C>G (p.Arg169Gly) | |
| 13 | g.42606631C>T | CA249053399 | TNFSF11 | c.667C>T (p.Arg223Ter) c.526C>T (p.Arg176Ter) c.448C>T (p.Arg150Ter) c.505C>T (p.Arg169Ter) | ClinVar dbSNP gnomAD v4 COSMIC |
| 13 | g.42606632G>A | CA6967281 | TNFSF11 | c.668G>A (p.Arg223Gln) c.527G>A (p.Arg176Gln) c.449G>A (p.Arg150Gln) c.506G>A (p.Arg169Gln) | dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC |
| 13 | g.42606632G>C | CA388221363 | TNFSF11 | c.668G>C (p.Arg223Pro) c.527G>C (p.Arg176Pro) c.449G>C (p.Arg150Pro) c.506G>C (p.Arg169Pro) | |
| 13 | g.42606632G= | CA2087395081 | TNFSF11 | c.668G= (p.Arg223=) c.527G= (p.Arg176=) c.449G= (p.Arg150=) c.506G= (p.Arg169=) | |
| 13 | g.42606632G>T | CA388221364 | TNFSF11 | c.668G>T (p.Arg223Leu) c.527G>T (p.Arg176Leu) c.449G>T (p.Arg150Leu) c.506G>T (p.Arg169Leu) | |
| 13 | g.42606633A>C | CA483605059 | TNFSF11 | c.669A>C (p.Arg223=) c.528A>C (p.Arg176=) c.450A>C (p.Arg150=) c.507A>C (p.Arg169=) | |
| 13 | g.42606633A>G | CA483605060 | TNFSF11 | c.669A>G (p.Arg223=) c.528A>G (p.Arg176=) c.450A>G (p.Arg150=) c.507A>G (p.Arg169=) | |
| 13 | g.42606633A>T | CA483605061 | TNFSF11 | c.669A>T (p.Arg223=) c.528A>T (p.Arg176=) c.450A>T (p.Arg150=) c.507A>T (p.Arg169=) | |
| 13 | g.42606634C>A | CA388221367 | TNFSF11 | c.670C>A (p.His224Asn) c.529C>A (p.His177Asn) c.451C>A (p.His151Asn) c.508C>A (p.His170Asn) | |
| 13 | g.42606634C>G | CA388221369 | TNFSF11 | c.670C>G (p.His224Asp) c.529C>G (p.His177Asp) c.451C>G (p.His151Asp) c.508C>G (p.His170Asp) | |
| 13 | g.42606634C>T | CA388221370 | TNFSF11 | c.670C>T (p.His224Tyr) c.529C>T (p.His177Tyr) c.451C>T (p.His151Tyr) c.508C>T (p.His170Tyr) | |
| 13 | g.42606635A= | CA2087395082 | TNFSF11 | c.671A= (p.His224=) c.530A= (p.His177=) c.452A= (p.His151=) c.509A= (p.His170=) | |
| 13 | g.42606635A>C | CA388221374 | TNFSF11 | c.671A>C (p.His224Pro) c.530A>C (p.His177Pro) c.452A>C (p.His151Pro) c.509A>C (p.His170Pro) | |
| 13 | g.42606635A>G | CA6967282 | TNFSF11 | c.671A>G (p.His224Arg) c.530A>G (p.His177Arg) c.452A>G (p.His151Arg) c.509A>G (p.His170Arg) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.42606635A>T | CA388221375 | TNFSF11 | c.671A>T (p.His224Leu) c.530A>T (p.His177Leu) c.452A>T (p.His151Leu) c.509A>T (p.His170Leu) | |
| 13 | g.42606636T>A | CA388221376 | TNFSF11 | c.672T>A (p.His224Gln) c.531T>A (p.His177Gln) c.453T>A (p.His151Gln) c.510T>A (p.His170Gln) | |
| 13 | g.42606636T>C | CA483605062 | TNFSF11 | c.672T>C (p.His224=) c.531T>C (p.His177=) c.453T>C (p.His151=) c.510T>C (p.His170=) | |
| 13 | g.42606636T>G | CA388221378 | TNFSF11 | c.672T>G (p.His224Gln) c.531T>G (p.His177Gln) c.453T>G (p.His151Gln) c.510T>G (p.His170Gln) | |
| 13 | g.42606637C>A | CA388221380 | TNFSF11 | c.673C>A (p.His225Asn) c.532C>A (p.His178Asn) c.454C>A (p.His152Asn) c.511C>A (p.His171Asn) | COSMIC |
| 13 | g.42606637C>G | CA388221381 | TNFSF11 | c.673C>G (p.His225Asp) c.532C>G (p.His178Asp) c.454C>G (p.His152Asp) c.511C>G (p.His171Asp) | |
| 13 | g.42606637C>T | CA388221384 | TNFSF11 | c.673C>T (p.His225Tyr) c.532C>T (p.His178Tyr) c.454C>T (p.His152Tyr) c.511C>T (p.His171Tyr) | |
| 13 | g.42606638A>C | CA388221386 | TNFSF11 | c.674A>C (p.His225Pro) c.533A>C (p.His178Pro) c.455A>C (p.His152Pro) c.512A>C (p.His171Pro) | |
| 13 | g.42606638A>G | CA388221388 | TNFSF11 | c.674A>G (p.His225Arg) c.533A>G (p.His178Arg) c.455A>G (p.His152Arg) c.512A>G (p.His171Arg) | |
| 13 | g.42606638A>T | CA388221390 | TNFSF11 | c.674A>T (p.His225Leu) c.533A>T (p.His178Leu) c.455A>T (p.His152Leu) c.512A>T (p.His171Leu) | |
| 13 | g.42606639T>A | CA388221392 | TNFSF11 | c.675T>A (p.His225Gln) c.534T>A (p.His178Gln) c.456T>A (p.His152Gln) c.513T>A (p.His171Gln) | |
| 13 | g.42606639T>C | CA483605063 | TNFSF11 | c.675T>C (p.His225=) c.534T>C (p.His178=) c.456T>C (p.His152=) c.513T>C (p.His171=) | gnomAD v4 |
| 13 | g.42606639T>G | CA388221394 | TNFSF11 | c.675T>G (p.His225Gln) c.534T>G (p.His178Gln) c.456T>G (p.His152Gln) c.513T>G (p.His171Gln) | |
| 13 | g.42606640G>A | CA388221397 | TNFSF11 | c.676G>A (p.Glu226Lys) c.535G>A (p.Glu179Lys) c.457G>A (p.Glu153Lys) c.514G>A (p.Glu172Lys) | COSMIC |
| 13 | g.42606640G>C | CA388221398 | TNFSF11 | c.676G>C (p.Glu226Gln) c.535G>C (p.Glu179Gln) c.457G>C (p.Glu153Gln) c.514G>C (p.Glu172Gln) | |
| 13 | g.42606640G>T | CA388221400 | TNFSF11 | c.676G>T (p.Glu226Ter) c.535G>T (p.Glu179Ter) c.457G>T (p.Glu153Ter) c.514G>T (p.Glu172Ter) | COSMIC |
| 13 | g.42606641A>C | CA388221405 | TNFSF11 | c.677A>C (p.Glu226Ala) c.536A>C (p.Glu179Ala) c.458A>C (p.Glu153Ala) c.515A>C (p.Glu172Ala) | |
| 13 | g.42606641A>G | CA388221402 | TNFSF11 | c.677A>G (p.Glu226Gly) c.536A>G (p.Glu179Gly) c.458A>G (p.Glu153Gly) c.515A>G (p.Glu172Gly) | |
| 13 | g.42606641A>T | CA388221404 | TNFSF11 | c.677A>T (p.Glu226Val) c.536A>T (p.Glu179Val) c.458A>T (p.Glu153Val) c.515A>T (p.Glu172Val) | |
| 13 | g.42606642A>C | CA388221406 | TNFSF11 | c.678A>C (p.Glu226Asp) c.537A>C (p.Glu179Asp) c.459A>C (p.Glu153Asp) c.516A>C (p.Glu172Asp) | |
| 13 | g.42606642A>G | CA483605064 | TNFSF11 | c.678A>G (p.Glu226=) c.537A>G (p.Glu179=) c.459A>G (p.Glu153=) c.516A>G (p.Glu172=) | |
| 13 | g.42606642A>T | CA388221408 | TNFSF11 | c.678A>T (p.Glu226Asp) c.537A>T (p.Glu179Asp) c.459A>T (p.Glu153Asp) c.516A>T (p.Glu172Asp) | |
| 13 | g.42606643A= | CA2087395083 | TNFSF11 | c.679A= (p.Thr227=) c.538A= (p.Thr180=) c.460A= (p.Thr154=) c.517A= (p.Thr173=) | |
| 13 | g.42606643A>C | CA388221411 | TNFSF11 | c.679A>C (p.Thr227Pro) c.538A>C (p.Thr180Pro) c.460A>C (p.Thr154Pro) c.517A>C (p.Thr173Pro) | |
| 13 | g.42606643A>G | CA6967283 | TNFSF11 | c.679A>G (p.Thr227Ala) c.538A>G (p.Thr180Ala) c.460A>G (p.Thr154Ala) c.517A>G (p.Thr173Ala) | dbSNP ExAC |
| 13 | g.42606643A>T | CA388221414 | TNFSF11 | c.679A>T (p.Thr227Ser) c.538A>T (p.Thr180Ser) c.460A>T (p.Thr154Ser) c.517A>T (p.Thr173Ser) | |
| 13 | g.42606644C>A | CA388221417 | TNFSF11 | c.680C>A (p.Thr227Asn) c.539C>A (p.Thr180Asn) c.461C>A (p.Thr154Asn) c.518C>A (p.Thr173Asn) | |
| 13 | g.42606644C>G | CA388221419 | TNFSF11 | c.680C>G (p.Thr227Ser) c.539C>G (p.Thr180Ser) c.461C>G (p.Thr154Ser) c.518C>G (p.Thr173Ser) | |
| 13 | g.42606644C>T | CA388221421 | TNFSF11 | c.680C>T (p.Thr227Ile) c.539C>T (p.Thr180Ile) c.461C>T (p.Thr154Ile) c.518C>T (p.Thr173Ile) | |
| 13 | g.42606645T>A | CA483605066 | TNFSF11 | c.681T>A (p.Thr227=) c.540T>A (p.Thr180=) c.462T>A (p.Thr154=) c.519T>A (p.Thr173=) | |
| 13 | g.42606645T>C | CA483605067 | TNFSF11 | c.681T>C (p.Thr227=) c.540T>C (p.Thr180=) c.462T>C (p.Thr154=) c.519T>C (p.Thr173=) | |
| 13 | g.42606645T>G | CA483605065 | TNFSF11 | c.681T>G (p.Thr227=) c.540T>G (p.Thr180=) c.462T>G (p.Thr154=) c.519T>G (p.Thr173=) | dbSNP gnomAD v2 gnomAD v4 |
| 13 | g.42606645T= | CA2087395084 | TNFSF11 | c.681T= (p.Thr227=) c.540T= (p.Thr180=) c.462T= (p.Thr154=) c.519T= (p.Thr173=) | |
| 13 | g.42606646T>A | CA388221424 | TNFSF11 | c.682T>A (p.Ser228Thr) c.541T>A (p.Ser181Thr) c.463T>A (p.Ser155Thr) c.520T>A (p.Ser174Thr) | |
| 13 | g.42606646T>C | CA388221425 | TNFSF11 | c.682T>C (p.Ser228Pro) c.541T>C (p.Ser181Pro) c.463T>C (p.Ser155Pro) c.520T>C (p.Ser174Pro) | |
| 13 | g.42606646T>G | CA388221426 | TNFSF11 | c.682T>G (p.Ser228Ala) c.541T>G (p.Ser181Ala) c.463T>G (p.Ser155Ala) c.520T>G (p.Ser174Ala) | |
| 13 | g.42606647C>A | CA388221428 | TNFSF11 | c.683C>A (p.Ser228Ter) c.542C>A (p.Ser181Ter) c.464C>A (p.Ser155Ter) c.521C>A (p.Ser174Ter) | |
| 13 | g.42606647C= | CA2087395085 | TNFSF11 | c.683C= (p.Ser228=) c.542C= (p.Ser181=) c.464C= (p.Ser155=) c.521C= (p.Ser174=) | |
| 13 | g.42606647C>G | CA388221432 | TNFSF11 | c.683C>G (p.Ser228Ter) c.542C>G (p.Ser181Ter) c.464C>G (p.Ser155Ter) c.521C>G (p.Ser174Ter) | |
| 13 | g.42606647C>T | CA388221430 | TNFSF11 | c.683C>T (p.Ser228Leu) c.542C>T (p.Ser181Leu) c.464C>T (p.Ser155Leu) c.521C>T (p.Ser174Leu) | dbSNP gnomAD v4 |
| 13 | g.42606648A= | CA2087395086 | TNFSF11 | c.684A= (p.Ser228=) c.543A= (p.Ser181=) c.465A= (p.Ser155=) c.522A= (p.Ser174=) | |
| 13 | g.42606648A>C | CA6967284 | TNFSF11 | c.684A>C (p.Ser228=) c.543A>C (p.Ser181=) c.465A>C (p.Ser155=) c.522A>C (p.Ser174=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.42606648A>G | CA483605068 | TNFSF11 | c.684A>G (p.Ser228=) c.543A>G (p.Ser181=) c.465A>G (p.Ser155=) c.522A>G (p.Ser174=) | |
| 13 | g.42606648A>T | CA483605069 | TNFSF11 | c.684A>T (p.Ser228=) c.543A>T (p.Ser181=) c.465A>T (p.Ser155=) c.522A>T (p.Ser174=) | |
| 13 | g.42606649G>A | CA388221440 | TNFSF11 | c.685G>A (p.Gly229Arg) c.544G>A (p.Gly182Arg) c.466G>A (p.Gly156Arg) c.523G>A (p.Gly175Arg) | dbSNP gnomAD v4 |
| 13 | g.42606649G>C | CA388221436 | TNFSF11 | c.685G>C (p.Gly229Arg) c.544G>C (p.Gly182Arg) c.466G>C (p.Gly156Arg) c.523G>C (p.Gly175Arg) | |
| 13 | g.42606649G= | CA2087395087 | TNFSF11 | c.685G= (p.Gly229=) c.544G= (p.Gly182=) c.466G= (p.Gly156=) c.523G= (p.Gly175=) | |
| 13 | g.42606649G>T | CA388221438 | TNFSF11 | c.685G>T (p.Gly229Ter) c.544G>T (p.Gly182Ter) c.466G>T (p.Gly156Ter) c.523G>T (p.Gly175Ter) | |
| 13 | g.42606650G>A | CA388221442 | TNFSF11 | c.686G>A (p.Gly229Glu) c.545G>A (p.Gly182Glu) c.467G>A (p.Gly156Glu) c.524G>A (p.Gly175Glu) | |
| 13 | g.42606650G>C | CA388221445 | TNFSF11 | c.686G>C (p.Gly229Ala) c.545G>C (p.Gly182Ala) c.467G>C (p.Gly156Ala) c.524G>C (p.Gly175Ala) | |
| 13 | g.42606650G>T | CA388221446 | TNFSF11 | c.686G>T (p.Gly229Val) c.545G>T (p.Gly182Val) c.467G>T (p.Gly156Val) c.524G>T (p.Gly175Val) | |
| 13 | g.42606651A>C | CA483605070 | TNFSF11 | c.687A>C (p.Gly229=) c.546A>C (p.Gly182=) c.468A>C (p.Gly156=) c.525A>C (p.Gly175=) | |
| 13 | g.42606651A>G | CA483605072 | TNFSF11 | c.687A>G (p.Gly229=) c.546A>G (p.Gly182=) c.468A>G (p.Gly156=) c.525A>G (p.Gly175=) | gnomAD v4 |
| 13 | g.42606651A>T | CA483605071 | TNFSF11 | c.687A>T (p.Gly229=) c.546A>T (p.Gly182=) c.468A>T (p.Gly156=) c.525A>T (p.Gly175=) | |
| 13 | g.42606652G>A | CA388221449 | TNFSF11 | c.688G>A (p.Asp230Asn) c.547G>A (p.Asp183Asn) c.469G>A (p.Asp157Asn) c.526G>A (p.Asp176Asn) | |
| 13 | g.42606652G>C | CA388221451 | TNFSF11 | c.688G>C (p.Asp230His) c.547G>C (p.Asp183His) c.469G>C (p.Asp157His) c.526G>C (p.Asp176His) | |
| 13 | g.42606652G>T | CA388221452 | TNFSF11 | c.688G>T (p.Asp230Tyr) c.547G>T (p.Asp183Tyr) c.469G>T (p.Asp157Tyr) c.526G>T (p.Asp176Tyr) | |
| 13 | g.42606653A>C | CA388221456 | TNFSF11 | c.689A>C (p.Asp230Ala) c.548A>C (p.Asp183Ala) c.470A>C (p.Asp157Ala) c.527A>C (p.Asp176Ala) | |
| 13 | g.42606653A>G | CA388221457 | TNFSF11 | c.689A>G (p.Asp230Gly) c.548A>G (p.Asp183Gly) c.470A>G (p.Asp157Gly) c.527A>G (p.Asp176Gly) | |
| 13 | g.42606653A>T | CA388221460 | TNFSF11 | c.689A>T (p.Asp230Val) c.548A>T (p.Asp183Val) c.470A>T (p.Asp157Val) c.527A>T (p.Asp176Val) | |
| 13 | g.42606654C>A | CA388221464 | TNFSF11 | c.690C>A (p.Asp230Glu) c.549C>A (p.Asp183Glu) c.471C>A (p.Asp157Glu) c.528C>A (p.Asp176Glu) | |
| 13 | g.42606654C>G | CA388221462 | TNFSF11 | c.690C>G (p.Asp230Glu) c.549C>G (p.Asp183Glu) c.471C>G (p.Asp157Glu) c.528C>G (p.Asp176Glu) | |
| 13 | g.42606654C>T | CA483605073 | TNFSF11 | c.690C>T (p.Asp230=) c.549C>T (p.Asp183=) c.471C>T (p.Asp157=) c.528C>T (p.Asp176=) | |
| 13 | g.42606655del | CA2622837737 | TNFSF11 | c.691del (p.Leu231Ter) c.550del (p.Leu184Ter) c.472del (p.Leu158Ter) c.529del (p.Leu177Ter) | gnomAD v4 |
| 13 | g.42606655C>A | CA388221467 | TNFSF11 | c.691C>A (p.Leu231Ile) c.550C>A (p.Leu184Ile) c.472C>A (p.Leu158Ile) c.529C>A (p.Leu177Ile) | gnomAD v4 |
| 13 | g.42606655C>G | CA388221468 | TNFSF11 | c.691C>G (p.Leu231Val) c.550C>G (p.Leu184Val) c.472C>G (p.Leu158Val) c.529C>G (p.Leu177Val) | |
| 13 | g.42606655C>T | CA483605074 | TNFSF11 | c.691C>T (p.Leu231=) c.550C>T (p.Leu184=) c.472C>T (p.Leu158=) c.529C>T (p.Leu177=) | |
| 13 | g.42606656T>A | CA388221471 | TNFSF11 | c.692T>A (p.Leu231Gln) c.551T>A (p.Leu184Gln) c.473T>A (p.Leu158Gln) c.530T>A (p.Leu177Gln) | |
| 13 | g.42606656T>C | CA388221473 | TNFSF11 | c.692T>C (p.Leu231Pro) c.551T>C (p.Leu184Pro) c.473T>C (p.Leu158Pro) c.530T>C (p.Leu177Pro) | |
| 13 | g.42606656T>G | CA388221475 | TNFSF11 | c.692T>G (p.Leu231Arg) c.551T>G (p.Leu184Arg) c.473T>G (p.Leu158Arg) c.530T>G (p.Leu177Arg) | |
| 13 | g.42606657A>C | CA483605075 | TNFSF11 | c.693A>C (p.Leu231=) c.552A>C (p.Leu184=) c.474A>C (p.Leu158=) c.531A>C (p.Leu177=) | |
| 13 | g.42606657A>G | CA483605076 | TNFSF11 | c.693A>G (p.Leu231=) c.552A>G (p.Leu184=) c.474A>G (p.Leu158=) c.531A>G (p.Leu177=) | |
| 13 | g.42606657A>T | CA483605077 | TNFSF11 | c.693A>T (p.Leu231=) c.552A>T (p.Leu184=) c.474A>T (p.Leu158=) c.531A>T (p.Leu177=) | |
| 13 | g.42606658G>A | CA388221477 | TNFSF11 | c.694G>A (p.Ala232Thr) c.553G>A (p.Ala185Thr) c.475G>A (p.Ala159Thr) c.532G>A (p.Ala178Thr) | gnomAD v4 |
| 13 | g.42606658G>C | CA388221479 | TNFSF11 | c.694G>C (p.Ala232Pro) c.553G>C (p.Ala185Pro) c.475G>C (p.Ala159Pro) c.532G>C (p.Ala178Pro) | |
| 13 | g.42606658G>T | CA388221481 | TNFSF11 | c.694G>T (p.Ala232Ser) c.553G>T (p.Ala185Ser) c.475G>T (p.Ala159Ser) c.532G>T (p.Ala178Ser) | |
| 13 | g.42606659C>A | CA388221483 | TNFSF11 | c.695C>A (p.Ala232Asp) c.554C>A (p.Ala185Asp) c.476C>A (p.Ala159Asp) c.533C>A (p.Ala178Asp) | |
| 13 | g.42606659C>G | CA388221485 | TNFSF11 | c.695C>G (p.Ala232Gly) c.554C>G (p.Ala185Gly) c.476C>G (p.Ala159Gly) c.533C>G (p.Ala178Gly) | |
| 13 | g.42606659C>T | CA388221488 | TNFSF11 | c.695C>T (p.Ala232Val) c.554C>T (p.Ala185Val) c.476C>T (p.Ala159Val) c.533C>T (p.Ala178Val) | |
| 13 | g.42606660T>A | CA6967285 | TNFSF11 | c.696T>A (p.Ala232=) c.555T>A (p.Ala185=) c.477T>A (p.Ala159=) c.534T>A (p.Ala178=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.42606660T>C | CA483741646 | TNFSF11 | c.696T>C (p.Ala232=) c.555T>C (p.Ala185=) c.477T>C (p.Ala159=) c.534T>C (p.Ala178=) | |
| 13 | g.42606660T>G | CA483741647 | TNFSF11 | c.696T>G (p.Ala232=) c.555T>G (p.Ala185=) c.477T>G (p.Ala159=) c.534T>G (p.Ala178=) | |
| 13 | g.42606660T= | CA2087395088 | TNFSF11 | c.696T= (p.Ala232=) c.555T= (p.Ala185=) c.477T= (p.Ala159=) c.534T= (p.Ala178=) | |
| 13 | g.42606661A>C | CA388221493 | TNFSF11 | c.697A>C (p.Thr233Pro) c.556A>C (p.Thr186Pro) c.478A>C (p.Thr160Pro) c.535A>C (p.Thr179Pro) | |
| 13 | g.42606661A>G | CA388221495 | TNFSF11 | c.697A>G (p.Thr233Ala) c.556A>G (p.Thr186Ala) c.478A>G (p.Thr160Ala) c.535A>G (p.Thr179Ala) | |
| 13 | g.42606661A>T | CA388221491 | TNFSF11 | c.697A>T (p.Thr233Ser) c.556A>T (p.Thr186Ser) c.478A>T (p.Thr160Ser) c.535A>T (p.Thr179Ser) | |
| 13 | g.42606661_42606662insAAAGT | CA2516453911 | TNFSF11 | c.697_698insAAAGT (p.Thr233LysfsTer8) c.556_557insAAAGT (p.Thr186LysfsTer8) c.478_479insAAAGT (p.Thr160LysfsTer8) c.535_536insAAAGT (p.Thr179LysfsTer8) | |
| 13 | g.42606662C>A | CA388221497 | TNFSF11 | c.698C>A (p.Thr233Lys) c.557C>A (p.Thr186Lys) c.479C>A (p.Thr160Lys) c.536C>A (p.Thr179Lys) | gnomAD v4 |
| 13 | g.42606662C>G | CA388221499 | TNFSF11 | c.698C>G (p.Thr233Arg) c.557C>G (p.Thr186Arg) c.479C>G (p.Thr160Arg) c.536C>G (p.Thr179Arg) | |
| 13 | g.42606662C>T | CA388221501 | TNFSF11 | c.698C>T (p.Thr233Ile) c.557C>T (p.Thr186Ile) c.479C>T (p.Thr160Ile) c.536C>T (p.Thr179Ile) | |
| 13 | g.42606663A= | CA2087395089 | TNFSF11 | c.699A= (p.Thr233=) c.558A= (p.Thr186=) c.480A= (p.Thr160=) c.537A= (p.Thr179=) | |
| 13 | g.42606663A>C | CA483741648 | TNFSF11 | c.699A>C (p.Thr233=) c.558A>C (p.Thr186=) c.480A>C (p.Thr160=) c.537A>C (p.Thr179=) | dbSNP gnomAD v2 gnomAD v4 |
| 13 | g.42606663A>G | CA483741649 | TNFSF11 | c.699A>G (p.Thr233=) c.558A>G (p.Thr186=) c.480A>G (p.Thr160=) c.537A>G (p.Thr179=) | gnomAD v4 |
| 13 | g.42606663A>T | CA483741650 | TNFSF11 | c.699A>T (p.Thr233=) c.558A>T (p.Thr186=) c.480A>T (p.Thr160=) c.537A>T (p.Thr179=) | |
| 13 | g.42606663_42606664insTGTTGGA | CA2554309887 | TNFSF11 | c.699_700insTGTTGGA (p.Glu234CysfsTer13) c.558_559insTGTTGGA (p.Glu187CysfsTer13) c.480_481insTGTTGGA (p.Glu161CysfsTer13) c.537_538insTGTTGGA (p.Glu180CysfsTer13) | |
| 13 | g.42606664G>A | CA249053400 | TNFSF11 | c.700G>A (p.Glu234Lys) c.559G>A (p.Glu187Lys) c.481G>A (p.Glu161Lys) c.538G>A (p.Glu180Lys) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.42606664G>C | CA388221505 | TNFSF11 | c.700G>C (p.Glu234Gln) c.559G>C (p.Glu187Gln) c.481G>C (p.Glu161Gln) c.538G>C (p.Glu180Gln) | dbSNP gnomAD v4 |
| 13 | g.42606664G= | CA2087395090 | TNFSF11 | c.700G= (p.Glu234=) c.559G= (p.Glu187=) c.481G= (p.Glu161=) c.538G= (p.Glu180=) | |
| 13 | g.42606664G>T | CA388221507 | TNFSF11 | c.700G>T (p.Glu234Ter) c.559G>T (p.Glu187Ter) c.481G>T (p.Glu161Ter) c.538G>T (p.Glu180Ter) | |
| 13 | g.42606665A>C | CA388221509 | TNFSF11 | c.701A>C (p.Glu234Ala) c.560A>C (p.Glu187Ala) c.482A>C (p.Glu161Ala) c.539A>C (p.Glu180Ala) | |
| 13 | g.42606665A>G | CA388221512 | TNFSF11 | c.701A>G (p.Glu234Gly) c.560A>G (p.Glu187Gly) c.482A>G (p.Glu161Gly) c.539A>G (p.Glu180Gly) | |
| 13 | g.42606665A>T | CA388221514 | TNFSF11 | c.701A>T (p.Glu234Val) c.560A>T (p.Glu187Val) c.482A>T (p.Glu161Val) c.539A>T (p.Glu180Val) |