| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 9 | g.91724805T>A | CA373797772 | ROR2 | c.1689A>T (p.Glu563Asp) c.1269A>T (p.Glu423Asp) n.2157A>T c.486A>T (p.Glu162Asp) c.1680A>T (p.Glu560Asp) | dbSNP gnomAD v4 |
| 9 | g.91724805T>C | CA466339211 | ROR2 | c.1689A>G (p.Glu563=) c.1269A>G (p.Glu423=) n.2157A>G c.486A>G (p.Glu162=) c.1680A>G (p.Glu560=) | dbSNP gnomAD v2 gnomAD v4 |
| 9 | g.91724805T>G | CA373797773 | ROR2 | c.1689A>C (p.Glu563Asp) c.1269A>C (p.Glu423Asp) n.2157A>C c.486A>C (p.Glu162Asp) c.1680A>C (p.Glu560Asp) | |
| 9 | g.91724805T= | CA1863923306 | ROR2 | c.1689A= (p.Glu563=) c.1269A= (p.Glu423=) n.2157A= c.486A= (p.Glu162=) c.1680A= (p.Glu560=) | |
| 9 | g.91724806T>A | CA373797775 | ROR2 | c.1688A>T (p.Glu563Val) c.1268A>T (p.Glu423Val) n.2156A>T c.485A>T (p.Glu162Val) c.1679A>T (p.Glu560Val) | |
| 9 | g.91724806T>C | CA5120609 | ROR2 | c.1688A>G (p.Glu563Gly) c.1268A>G (p.Glu423Gly) n.2156A>G c.485A>G (p.Glu162Gly) c.1679A>G (p.Glu560Gly) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 9 | g.91724806T>G | CA373797774 | ROR2 | c.1688A>C (p.Glu563Ala) c.1268A>C (p.Glu423Ala) n.2156A>C c.485A>C (p.Glu162Ala) c.1679A>C (p.Glu560Ala) | |
| 9 | g.91724806T= | CA1863923307 | ROR2 | c.1688A= (p.Glu563=) c.1268A= (p.Glu423=) n.2156A= c.485A= (p.Glu162=) c.1679A= (p.Glu560=) | |
| 9 | g.91724807C>A | CA373797776 | ROR2 | c.1687G>T (p.Glu563Ter) c.1267G>T (p.Glu423Ter) n.2155G>T c.484G>T (p.Glu162Ter) c.1678G>T (p.Glu560Ter) | |
| 9 | g.91724807C= | CA1863923309 | ROR2 | c.1687G= (p.Glu563=) c.1267G= (p.Glu423=) n.2155G= c.484G= (p.Glu162=) c.1678G= (p.Glu560=) | |
| 9 | g.91724807C>G | CA373797777 | ROR2 | c.1687G>C (p.Glu563Gln) c.1267G>C (p.Glu423Gln) n.2155G>C c.484G>C (p.Glu162Gln) c.1678G>C (p.Glu560Gln) | |
| 9 | g.91724807C>T | CA5120610 | ROR2 | c.1687G>A (p.Glu563Lys) c.1267G>A (p.Glu423Lys) n.2155G>A c.484G>A (p.Glu162Lys) c.1678G>A (p.Glu560Lys) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 9 | g.91724808G>A | CA5120611 | ROR2 | c.1686C>T (p.His562=) c.1266C>T (p.His422=) n.2154C>T c.483C>T (p.His161=) c.1677C>T (p.His559=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 9 | g.91724808G>C | CA373797778 | ROR2 | c.1686C>G (p.His562Gln) c.1266C>G (p.His422Gln) n.2154C>G c.483C>G (p.His161Gln) c.1677C>G (p.His559Gln) | gnomAD v4 |
| 9 | g.91724808G= | CA1863923311 | ROR2 | c.1686C= (p.His562=) c.1266C= (p.His422=) n.2154C= c.483C= (p.His161=) c.1677C= (p.His559=) | |
| 9 | g.91724808G>T | CA373797779 | ROR2 | c.1686C>A (p.His562Gln) c.1266C>A (p.His422Gln) n.2154C>A c.483C>A (p.His161Gln) c.1677C>A (p.His559Gln) | |
| 9 | g.91724809T>A | CA373797780 | ROR2 | c.1685A>T (p.His562Leu) c.1265A>T (p.His422Leu) n.2153A>T c.482A>T (p.His161Leu) c.1676A>T (p.His559Leu) | gnomAD v4 |
| 9 | g.91724809T>C | CA373797781 | ROR2 | c.1685A>G (p.His562Arg) c.1265A>G (p.His422Arg) n.2153A>G c.482A>G (p.His161Arg) c.1676A>G (p.His559Arg) | |
| 9 | g.91724809T>G | CA373797782 | ROR2 | c.1685A>C (p.His562Pro) c.1265A>C (p.His422Pro) n.2153A>C c.482A>C (p.His161Pro) c.1676A>C (p.His559Pro) | |
| 9 | g.91724810G>A | CA373797783 | ROR2 | c.1684C>T (p.His562Tyr) c.1264C>T (p.His422Tyr) n.2152C>T c.481C>T (p.His161Tyr) c.1675C>T (p.His559Tyr) | |
| 9 | g.91724810G>C | CA373797784 | ROR2 | c.1684C>G (p.His562Asp) c.1264C>G (p.His422Asp) n.2152C>G c.481C>G (p.His161Asp) c.1675C>G (p.His559Asp) | |
| 9 | g.91724810G>T | CA373797785 | ROR2 | c.1684C>A (p.His562Asn) c.1264C>A (p.His422Asn) n.2152C>A c.481C>A (p.His161Asn) c.1675C>A (p.His559Asn) | |
| 9 | g.91724811G>A | CA466339215 | ROR2 | c.1683C>T (p.Leu561=) c.1263C>T (p.Leu421=) n.2151C>T c.480C>T (p.Leu160=) c.1674C>T (p.Leu558=) | |
| 9 | g.91724811G>C | CA466339216 | ROR2 | c.1683C>G (p.Leu561=) c.1263C>G (p.Leu421=) n.2151C>G c.480C>G (p.Leu160=) c.1674C>G (p.Leu558=) | |
| 9 | g.91724811G>T | CA466339217 | ROR2 | c.1683C>A (p.Leu561=) c.1263C>A (p.Leu421=) n.2151C>A c.480C>A (p.Leu160=) c.1674C>A (p.Leu558=) | |
| 9 | g.91724812A>C | CA373797786 | ROR2 | c.1682T>G (p.Leu561Arg) c.1262T>G (p.Leu421Arg) n.2150T>G c.479T>G (p.Leu160Arg) c.1673T>G (p.Leu558Arg) | |
| 9 | g.91724812A>G | CA373797788 | ROR2 | c.1682T>C (p.Leu561Pro) c.1262T>C (p.Leu421Pro) n.2150T>C c.479T>C (p.Leu160Pro) c.1673T>C (p.Leu558Pro) | |
| 9 | g.91724812A>T | CA373797787 | ROR2 | c.1682T>A (p.Leu561His) c.1262T>A (p.Leu421His) n.2150T>A c.479T>A (p.Leu160His) c.1673T>A (p.Leu558His) | |
| 9 | g.91724813G>A | CA373797789 | ROR2 | c.1681C>T (p.Leu561Phe) c.1261C>T (p.Leu421Phe) n.2149C>T c.478C>T (p.Leu160Phe) c.1672C>T (p.Leu558Phe) | ClinVar dbSNP gnomAD v4 |
| 9 | g.91724813G>C | CA373797791 | ROR2 | c.1681C>G (p.Leu561Val) c.1261C>G (p.Leu421Val) n.2149C>G c.478C>G (p.Leu160Val) c.1672C>G (p.Leu558Val) | gnomAD v4 |
| 9 | g.91724813G= | CA1863923314 | ROR2 | c.1681C= (p.Leu561=) c.1261C= (p.Leu421=) n.2149C= c.478C= (p.Leu160=) c.1672C= (p.Leu558=) | |
| 9 | g.91724813G>T | CA373797790 | ROR2 | c.1681C>A (p.Leu561Ile) c.1261C>A (p.Leu421Ile) n.2149C>A c.478C>A (p.Leu160Ile) c.1672C>A (p.Leu558Ile) | |
| 9 | g.91724814G>A | CA466339220 | ROR2 | c.1680C>T (p.Asp560=) c.1260C>T (p.Asp420=) n.2148C>T c.477C>T (p.Asp159=) c.1671C>T (p.Asp557=) | |
| 9 | g.91724814G>C | CA373797792 | ROR2 | c.1680C>G (p.Asp560Glu) c.1260C>G (p.Asp420Glu) n.2148C>G c.477C>G (p.Asp159Glu) c.1671C>G (p.Asp557Glu) | |
| 9 | g.91724814G>T | CA373797793 | ROR2 | c.1680C>A (p.Asp560Glu) c.1260C>A (p.Asp420Glu) n.2148C>A c.477C>A (p.Asp159Glu) c.1671C>A (p.Asp557Glu) | |
| 9 | g.91724815T>A | CA373797794 | ROR2 | c.1679A>T (p.Asp560Val) c.1259A>T (p.Asp420Val) n.2147A>T c.476A>T (p.Asp159Val) c.1670A>T (p.Asp557Val) | |
| 9 | g.91724815T>C | CA373797795 | ROR2 | c.1679A>G (p.Asp560Gly) c.1259A>G (p.Asp420Gly) n.2147A>G c.476A>G (p.Asp159Gly) c.1670A>G (p.Asp557Gly) | |
| 9 | g.91724815T>G | CA373797796 | ROR2 | c.1679A>C (p.Asp560Ala) c.1259A>C (p.Asp420Ala) n.2147A>C c.476A>C (p.Asp159Ala) c.1670A>C (p.Asp557Ala) | |
| 9 | g.91724816C>A | CA373797797 | ROR2 | c.1678G>T (p.Asp560Tyr) c.1258G>T (p.Asp420Tyr) n.2146G>T c.475G>T (p.Asp159Tyr) c.1669G>T (p.Asp557Tyr) | gnomAD v4 |
| 9 | g.91724816C= | CA1863923316 | ROR2 | c.1678G= (p.Asp560=) c.1258G= (p.Asp420=) n.2146G= c.475G= (p.Asp159=) c.1669G= (p.Asp557=) | |
| 9 | g.91724816C>G | CA373797798 | ROR2 | c.1678G>C (p.Asp560His) c.1258G>C (p.Asp420His) n.2146G>C c.475G>C (p.Asp159His) c.1669G>C (p.Asp557His) | |
| 9 | g.91724816C>T | CA195323705 | ROR2 | c.1678G>A (p.Asp560Asn) c.1258G>A (p.Asp420Asn) n.2146G>A c.475G>A (p.Asp159Asn) c.1669G>A (p.Asp557Asn) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 9 | g.91724817G>A | CA5120612 | ROR2 | c.1677C>T (p.Gly559=) c.1257C>T (p.Gly419=) n.2145C>T c.474C>T (p.Gly158=) c.1668C>T (p.Gly556=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 9 | g.91724817G>C | CA466339224 | ROR2 | c.1677C>G (p.Gly559=) c.1257C>G (p.Gly419=) n.2145C>G c.474C>G (p.Gly158=) c.1668C>G (p.Gly556=) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 9 | g.91724817G= | CA1863923318 | ROR2 | c.1677C= (p.Gly559=) c.1257C= (p.Gly419=) n.2145C= c.474C= (p.Gly158=) c.1668C= (p.Gly556=) | |
| 9 | g.91724817G>T | CA466339225 | ROR2 | c.1677C>A (p.Gly559=) c.1257C>A (p.Gly419=) n.2145C>A c.474C>A (p.Gly158=) c.1668C>A (p.Gly556=) | |
| 9 | g.91724818_91724856dup | CA2573144756 | ROR2 | c.1639_1677dup (p.Gly559_Asp560insGlnProLeuSerMetIlePheSerTyrCysSerHisGly) c.1219_1257dup (p.Gly419_Asp420insGlnProLeuSerMetIlePheSerTyrCysSerHisGly) n.2107_2145dup c.436_474dup (p.Gly158_Asp159insGlnProLeuSerMetIlePheSerTyrCysSerHisGly) c.1630_1668dup (p.Gly556_Asp557insGlnProLeuSerMetIlePheSerTyrCysSerHisGly) | ClinVar dbSNP |
| 9 | g.91724818C>A | CA373797799 | ROR2 | c.1676G>T (p.Gly559Val) c.1256G>T (p.Gly419Val) n.2144G>T c.473G>T (p.Gly158Val) c.1667G>T (p.Gly556Val) | |
| 9 | g.91724818C>G | CA373797800 | ROR2 | c.1676G>C (p.Gly559Ala) c.1256G>C (p.Gly419Ala) n.2144G>C c.473G>C (p.Gly158Ala) c.1667G>C (p.Gly556Ala) | |
| 9 | g.91724818C>T | CA373797801 | ROR2 | c.1676G>A (p.Gly559Asp) c.1256G>A (p.Gly419Asp) n.2144G>A c.473G>A (p.Gly158Asp) c.1667G>A (p.Gly556Asp) | gnomAD v4 |
| 9 | g.91724819C>A | CA373797803 | ROR2 | c.1675G>T (p.Gly559Cys) c.1255G>T (p.Gly419Cys) n.2143G>T c.472G>T (p.Gly158Cys) c.1666G>T (p.Gly556Cys) | |
| 9 | g.91724819C= | CA1863923320 | ROR2 | c.1675G= (p.Gly559=) c.1255G= (p.Gly419=) n.2143G= c.472G= (p.Gly158=) c.1666G= (p.Gly556=) | |
| 9 | g.91724819C>G | CA373797802 | ROR2 | c.1675G>C (p.Gly559Arg) c.1255G>C (p.Gly419Arg) n.2143G>C c.472G>C (p.Gly158Arg) c.1666G>C (p.Gly556Arg) | dbSNP gnomAD v2 gnomAD v4 |
| 9 | g.91724819C>T | CA5120613 | ROR2 | c.1675G>A (p.Gly559Ser) c.1255G>A (p.Gly419Ser) n.2143G>A c.472G>A (p.Gly158Ser) c.1666G>A (p.Gly556Ser) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 9 | g.91724820G>A | CA5120614 | ROR2 | c.1674C>T (p.His558=) c.1254C>T (p.His418=) n.2142C>T c.471C>T (p.His157=) c.1665C>T (p.His555=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 9 | g.91724820G>C | CA373797804 | ROR2 | c.1674C>G (p.His558Gln) c.1254C>G (p.His418Gln) n.2142C>G c.471C>G (p.His157Gln) c.1665C>G (p.His555Gln) | |
| 9 | g.91724820G= | CA1863923323 | ROR2 | c.1674C= (p.His558=) c.1254C= (p.His418=) n.2142C= c.471C= (p.His157=) c.1665C= (p.His555=) | |
| 9 | g.91724820G>T | CA373797805 | ROR2 | c.1674C>A (p.His558Gln) c.1254C>A (p.His418Gln) n.2142C>A c.471C>A (p.His157Gln) c.1665C>A (p.His555Gln) | |
| 9 | g.91724821T>A | CA373797806 | ROR2 | c.1673A>T (p.His558Leu) c.1253A>T (p.His418Leu) n.2141A>T c.470A>T (p.His157Leu) c.1664A>T (p.His555Leu) | gnomAD v4 |
| 9 | g.91724821T>C | CA373797807 | ROR2 | c.1673A>G (p.His558Arg) c.1253A>G (p.His418Arg) n.2141A>G c.470A>G (p.His157Arg) c.1664A>G (p.His555Arg) | |
| 9 | g.91724821T>G | CA373797808 | ROR2 | c.1673A>C (p.His558Pro) c.1253A>C (p.His418Pro) n.2141A>C c.470A>C (p.His157Pro) c.1664A>C (p.His555Pro) | |
| 9 | g.91724822G>A | CA373797809 | ROR2 | c.1672C>T (p.His558Tyr) c.1252C>T (p.His418Tyr) n.2140C>T c.469C>T (p.His157Tyr) c.1663C>T (p.His555Tyr) | |
| 9 | g.91724822G>C | CA373797810 | ROR2 | c.1672C>G (p.His558Asp) c.1252C>G (p.His418Asp) n.2140C>G c.469C>G (p.His157Asp) c.1663C>G (p.His555Asp) | |
| 9 | g.91724822G>T | CA373797811 | ROR2 | c.1672C>A (p.His558Asn) c.1252C>A (p.His418Asn) n.2140C>A c.469C>A (p.His157Asn) c.1663C>A (p.His555Asn) | |
| 9 | g.91724823C>A | CA466339229 | ROR2 | c.1671G>T (p.Ser557=) c.1251G>T (p.Ser417=) n.2139G>T c.468G>T (p.Ser156=) c.1662G>T (p.Ser554=) | dbSNP |
| 9 | g.91724823C= | CA1863923325 | ROR2 | c.1671G= (p.Ser557=) c.1251G= (p.Ser417=) n.2139G= c.468G= (p.Ser156=) c.1662G= (p.Ser554=) | |
| 9 | g.91724823C>G | CA466339230 | ROR2 | c.1671G>C (p.Ser557=) c.1251G>C (p.Ser417=) n.2139G>C c.468G>C (p.Ser156=) c.1662G>C (p.Ser554=) | |
| 9 | g.91724823C>T | CA5120615 | ROR2 | c.1671G>A (p.Ser557=) c.1251G>A (p.Ser417=) n.2139G>A c.468G>A (p.Ser156=) c.1662G>A (p.Ser554=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 9 | g.91724824G>A | CA5120616 | ROR2 | c.1670C>T (p.Ser557Leu) c.1250C>T (p.Ser417Leu) n.2138C>T c.467C>T (p.Ser156Leu) c.1661C>T (p.Ser554Leu) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 9 | g.91724824G>C | CA373797812 | ROR2 | c.1670C>G (p.Ser557Trp) c.1250C>G (p.Ser417Trp) n.2138C>G c.467C>G (p.Ser156Trp) c.1661C>G (p.Ser554Trp) | gnomAD v4 |
| 9 | g.91724824G= | CA1863923329 | ROR2 | c.1670C= (p.Ser557=) c.1250C= (p.Ser417=) n.2138C= c.467C= (p.Ser156=) c.1661C= (p.Ser554=) | |
| 9 | g.91724824G>T | CA195323747 | ROR2 | c.1670C>A (p.Ser557Ter) c.1250C>A (p.Ser417Ter) n.2138C>A c.467C>A (p.Ser156Ter) c.1661C>A (p.Ser554Ter) | dbSNP |
| 9 | g.91724825A>C | CA373797813 | ROR2 | c.1669T>G (p.Ser557Ala) c.1249T>G (p.Ser417Ala) n.2137T>G c.466T>G (p.Ser156Ala) c.1660T>G (p.Ser554Ala) | |
| 9 | g.91724825A>G | CA373797814 | ROR2 | c.1669T>C (p.Ser557Pro) c.1249T>C (p.Ser417Pro) n.2137T>C c.466T>C (p.Ser156Pro) c.1660T>C (p.Ser554Pro) | |
| 9 | g.91724825A>T | CA373797815 | ROR2 | c.1669T>A (p.Ser557Thr) c.1249T>A (p.Ser417Thr) n.2137T>A c.466T>A (p.Ser156Thr) c.1660T>A (p.Ser554Thr) | |
| 9 | g.91724826A>C | CA373797816 | ROR2 | c.1668T>G (p.Cys556Trp) c.1248T>G (p.Cys416Trp) n.2136T>G c.465T>G (p.Cys155Trp) c.1659T>G (p.Cys553Trp) | |
| 9 | g.91724826A>G | CA466339233 | ROR2 | c.1668T>C (p.Cys556=) c.1248T>C (p.Cys416=) n.2136T>C c.465T>C (p.Cys155=) c.1659T>C (p.Cys553=) | |
| 9 | g.91724826A>T | CA373797817 | ROR2 | c.1668T>A (p.Cys556Ter) c.1248T>A (p.Cys416Ter) n.2136T>A c.465T>A (p.Cys155Ter) c.1659T>A (p.Cys553Ter) | |
| 9 | g.91724827C>A | CA373797818 | ROR2 | c.1667G>T (p.Cys556Phe) c.1247G>T (p.Cys416Phe) n.2135G>T c.464G>T (p.Cys155Phe) c.1658G>T (p.Cys553Phe) | |
| 9 | g.91724827C= | CA1863923332 | ROR2 | c.1667G= (p.Cys556=) c.1247G= (p.Cys416=) n.2135G= c.464G= (p.Cys155=) c.1658G= (p.Cys553=) | |
| 9 | g.91724827C>G | CA5120617 | ROR2 | c.1667G>C (p.Cys556Ser) c.1247G>C (p.Cys416Ser) n.2135G>C c.464G>C (p.Cys155Ser) c.1658G>C (p.Cys553Ser) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 9 | g.91724827C>T | CA373797819 | ROR2 | c.1667G>A (p.Cys556Tyr) c.1247G>A (p.Cys416Tyr) n.2135G>A c.464G>A (p.Cys155Tyr) c.1658G>A (p.Cys553Tyr) | |
| 9 | g.91724828A>C | CA373797820 | ROR2 | c.1666T>G (p.Cys556Gly) c.1246T>G (p.Cys416Gly) n.2134T>G c.463T>G (p.Cys155Gly) c.1657T>G (p.Cys553Gly) | |
| 9 | g.91724828A>G | CA373797821 | ROR2 | c.1666T>C (p.Cys556Arg) c.1246T>C (p.Cys416Arg) n.2134T>C c.463T>C (p.Cys155Arg) c.1657T>C (p.Cys553Arg) | gnomAD v4 |
| 9 | g.91724828A>T | CA373797822 | ROR2 | c.1666T>A (p.Cys556Ser) c.1246T>A (p.Cys416Ser) n.2134T>A c.463T>A (p.Cys155Ser) c.1657T>A (p.Cys553Ser) | |
| 9 | g.91724829G>A | CA466339237 | ROR2 | c.1665C>T (p.Tyr555=) c.1245C>T (p.Tyr415=) n.2133C>T c.462C>T (p.Tyr154=) c.1656C>T (p.Tyr552=) | gnomAD v4 |
| 9 | g.91724829G>C | CA373797823 | ROR2 | c.1665C>G (p.Tyr555Ter) c.1245C>G (p.Tyr415Ter) n.2133C>G c.462C>G (p.Tyr154Ter) c.1656C>G (p.Tyr552Ter) | |
| 9 | g.91724829G>T | CA373797824 | ROR2 | c.1665C>A (p.Tyr555Ter) c.1245C>A (p.Tyr415Ter) n.2133C>A c.462C>A (p.Tyr154Ter) c.1656C>A (p.Tyr552Ter) | |
| 9 | g.91724830T>A | CA373797826 | ROR2 | c.1664A>T (p.Tyr555Phe) c.1244A>T (p.Tyr415Phe) n.2132A>T c.461A>T (p.Tyr154Phe) c.1655A>T (p.Tyr552Phe) | |
| 9 | g.91724830T>C | CA5120618 | ROR2 | c.1664A>G (p.Tyr555Cys) c.1244A>G (p.Tyr415Cys) n.2132A>G c.461A>G (p.Tyr154Cys) c.1655A>G (p.Tyr552Cys) | dbSNP ExAC gnomAD v2 |
| 9 | g.91724830T>G | CA373797825 | ROR2 | c.1664A>C (p.Tyr555Ser) c.1244A>C (p.Tyr415Ser) n.2132A>C c.461A>C (p.Tyr154Ser) c.1655A>C (p.Tyr552Ser) | |
| 9 | g.91724830T= | CA1863923333 | ROR2 | c.1664A= (p.Tyr555=) c.1244A= (p.Tyr415=) n.2132A= c.461A= (p.Tyr154=) c.1655A= (p.Tyr552=) | |
| 9 | g.91724831A>C | CA373797827 | ROR2 | c.1663T>G (p.Tyr555Asp) c.1243T>G (p.Tyr415Asp) n.2131T>G c.460T>G (p.Tyr154Asp) c.1654T>G (p.Tyr552Asp) | |
| 9 | g.91724831A>G | CA373797828 | ROR2 | c.1663T>C (p.Tyr555His) c.1243T>C (p.Tyr415His) n.2131T>C c.460T>C (p.Tyr154His) c.1654T>C (p.Tyr552His) | |
| 9 | g.91724831A>T | CA373797829 | ROR2 | c.1663T>A (p.Tyr555Asn) c.1243T>A (p.Tyr415Asn) n.2131T>A c.460T>A (p.Tyr154Asn) c.1654T>A (p.Tyr552Asn) | |
| 9 | g.91724832G>A | CA5120619 | ROR2 | c.1662C>T (p.Ser554=) c.1242C>T (p.Ser414=) n.2130C>T c.459C>T (p.Ser153=) c.1653C>T (p.Ser551=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 9 | g.91724832G>C | CA373797830 | ROR2 | c.1662C>G (p.Ser554Arg) c.1242C>G (p.Ser414Arg) n.2130C>G c.459C>G (p.Ser153Arg) c.1653C>G (p.Ser551Arg) | |
| 9 | g.91724832G= | CA1863923335 | ROR2 | c.1662C= (p.Ser554=) c.1242C= (p.Ser414=) n.2130C= c.459C= (p.Ser153=) c.1653C= (p.Ser551=) | |
| 9 | g.91724832G>T | CA373797831 | ROR2 | c.1662C>A (p.Ser554Arg) c.1242C>A (p.Ser414Arg) n.2130C>A c.459C>A (p.Ser153Arg) c.1653C>A (p.Ser551Arg) | |
| 9 | g.91724833C>A | CA373797832 | ROR2 | c.1661G>T (p.Ser554Ile) c.1241G>T (p.Ser414Ile) n.2129G>T c.458G>T (p.Ser153Ile) c.1652G>T (p.Ser551Ile) | |
| 9 | g.91724833C>G | CA373797833 | ROR2 | c.1661G>C (p.Ser554Thr) c.1241G>C (p.Ser414Thr) n.2129G>C c.458G>C (p.Ser153Thr) c.1652G>C (p.Ser551Thr) | |
| 9 | g.91724833C>T | CA373797834 | ROR2 | c.1661G>A (p.Ser554Asn) c.1241G>A (p.Ser414Asn) n.2129G>A c.458G>A (p.Ser153Asn) c.1652G>A (p.Ser551Asn) | |
| 9 | g.91724834T>A | CA373797835 | ROR2 | c.1660A>T (p.Ser554Cys) c.1240A>T (p.Ser414Cys) n.2128A>T c.457A>T (p.Ser153Cys) c.1651A>T (p.Ser551Cys) | |
| 9 | g.91724834T>C | CA373797836 | ROR2 | c.1660A>G (p.Ser554Gly) c.1240A>G (p.Ser414Gly) n.2128A>G c.457A>G (p.Ser153Gly) c.1651A>G (p.Ser551Gly) | |
| 9 | g.91724834T>G | CA373797837 | ROR2 | c.1660A>C (p.Ser554Arg) c.1240A>C (p.Ser414Arg) n.2128A>C c.457A>C (p.Ser153Arg) c.1651A>C (p.Ser551Arg) | dbSNP gnomAD v3 gnomAD v4 |
| 9 | g.91724834T= | CA1863923337 | ROR2 | c.1660A= (p.Ser554=) c.1240A= (p.Ser414=) n.2128A= c.457A= (p.Ser153=) c.1651A= (p.Ser551=) | |
| 9 | g.91724835G>A | CA466339242 | ROR2 | c.1659C>T (p.Phe553=) c.1239C>T (p.Phe413=) n.2127C>T c.456C>T (p.Phe152=) c.1650C>T (p.Phe550=) | COSMIC |
| 9 | g.91724835G>C | CA373797838 | ROR2 | c.1659C>G (p.Phe553Leu) c.1239C>G (p.Phe413Leu) n.2127C>G c.456C>G (p.Phe152Leu) c.1650C>G (p.Phe550Leu) | |
| 9 | g.91724835G= | CA1863923339 | ROR2 | c.1659C= (p.Phe553=) c.1239C= (p.Phe413=) n.2127C= c.456C= (p.Phe152=) c.1650C= (p.Phe550=) | |
| 9 | g.91724835G>T | CA195323829 | ROR2 | c.1659C>A (p.Phe553Leu) c.1239C>A (p.Phe413Leu) n.2127C>A c.456C>A (p.Phe152Leu) c.1650C>A (p.Phe550Leu) | dbSNP |
| 9 | g.91724836A>C | CA373797839 | ROR2 | c.1658T>G (p.Phe553Cys) c.1238T>G (p.Phe413Cys) n.2126T>G c.455T>G (p.Phe152Cys) c.1649T>G (p.Phe550Cys) | |
| 9 | g.91724836A>G | CA373797841 | ROR2 | c.1658T>C (p.Phe553Ser) c.1238T>C (p.Phe413Ser) n.2126T>C c.455T>C (p.Phe152Ser) c.1649T>C (p.Phe550Ser) | |
| 9 | g.91724836A>T | CA373797840 | ROR2 | c.1658T>A (p.Phe553Tyr) c.1238T>A (p.Phe413Tyr) n.2126T>A c.455T>A (p.Phe152Tyr) c.1649T>A (p.Phe550Tyr) | |
| 9 | g.91724837A>C | CA373797842 | ROR2 | c.1657T>G (p.Phe553Val) c.1237T>G (p.Phe413Val) n.2125T>G c.454T>G (p.Phe152Val) c.1648T>G (p.Phe550Val) | |
| 9 | g.91724837A>G | CA373797844 | ROR2 | c.1657T>C (p.Phe553Leu) c.1237T>C (p.Phe413Leu) n.2125T>C c.454T>C (p.Phe152Leu) c.1648T>C (p.Phe550Leu) | |
| 9 | g.91724837A>T | CA373797843 | ROR2 | c.1657T>A (p.Phe553Ile) c.1237T>A (p.Phe413Ile) n.2125T>A c.454T>A (p.Phe152Ile) c.1648T>A (p.Phe550Ile) | |
| 9 | g.91724838G>A | CA466339244 | ROR2 | c.1656C>T (p.Ile552=) c.1236C>T (p.Ile412=) n.2124C>T c.453C>T (p.Ile151=) c.1647C>T (p.Ile549=) | gnomAD v4 |
| 9 | g.91724838G>C | CA373797845 | ROR2 | c.1656C>G (p.Ile552Met) c.1236C>G (p.Ile412Met) n.2124C>G c.453C>G (p.Ile151Met) c.1647C>G (p.Ile549Met) | |
| 9 | g.91724838G>T | CA466339245 | ROR2 | c.1656C>A (p.Ile552=) c.1236C>A (p.Ile412=) n.2124C>A c.453C>A (p.Ile151=) c.1647C>A (p.Ile549=) | |
| 9 | g.91724839A>C | CA373797846 | ROR2 | c.1655T>G (p.Ile552Ser) c.1235T>G (p.Ile412Ser) n.2123T>G c.452T>G (p.Ile151Ser) c.1646T>G (p.Ile549Ser) | |
| 9 | g.91724839A>G | CA373797847 | ROR2 | c.1655T>C (p.Ile552Thr) c.1235T>C (p.Ile412Thr) n.2123T>C c.452T>C (p.Ile151Thr) c.1646T>C (p.Ile549Thr) | |
| 9 | g.91724839A>T | CA373797848 | ROR2 | c.1655T>A (p.Ile552Asn) c.1235T>A (p.Ile412Asn) n.2123T>A c.452T>A (p.Ile151Asn) c.1646T>A (p.Ile549Asn) | |
| 9 | g.91724840T>A | CA373797849 | ROR2 | c.1654A>T (p.Ile552Phe) c.1234A>T (p.Ile412Phe) n.2122A>T c.451A>T (p.Ile151Phe) c.1645A>T (p.Ile549Phe) | |
| 9 | g.91724840T>C | CA5120620 | ROR2 | c.1654A>G (p.Ile552Val) c.1234A>G (p.Ile412Val) n.2122A>G c.451A>G (p.Ile151Val) c.1645A>G (p.Ile549Val) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 9 | g.91724840T>G | CA373797850 | ROR2 | c.1654A>C (p.Ile552Leu) c.1234A>C (p.Ile412Leu) n.2122A>C c.451A>C (p.Ile151Leu) c.1645A>C (p.Ile549Leu) | |
| 9 | g.91724840T= | CA1863923341 | ROR2 | c.1654A= (p.Ile552=) c.1234A= (p.Ile412=) n.2122A= c.451A= (p.Ile151=) c.1645A= (p.Ile549=) | |
| 9 | g.91724841C>A | CA373797851 | ROR2 | c.1653G>T (p.Met551Ile) c.1233G>T (p.Met411Ile) n.2121G>T c.450G>T (p.Met150Ile) c.1644G>T (p.Met548Ile) | |
| 9 | g.91724841C= | CA1863923343 | ROR2 | c.1653G= (p.Met551=) c.1233G= (p.Met411=) n.2121G= c.450G= (p.Met150=) c.1644G= (p.Met548=) | |
| 9 | g.91724841C>G | CA5120621 | ROR2 | c.1653G>C (p.Met551Ile) c.1233G>C (p.Met411Ile) n.2121G>C c.450G>C (p.Met150Ile) c.1644G>C (p.Met548Ile) | dbSNP ExAC gnomAD v3 gnomAD v4 |
| 9 | g.91724841C>T | CA373797852 | ROR2 | c.1653G>A (p.Met551Ile) c.1233G>A (p.Met411Ile) n.2121G>A c.450G>A (p.Met150Ile) c.1644G>A (p.Met548Ile) | |
| 9 | g.91724842A>C | CA373797853 | ROR2 | c.1652T>G (p.Met551Arg) c.1232T>G (p.Met411Arg) n.2120T>G c.449T>G (p.Met150Arg) c.1643T>G (p.Met548Arg) | gnomAD v4 |
| 9 | g.91724842A>G | CA373797854 | ROR2 | c.1652T>C (p.Met551Thr) c.1232T>C (p.Met411Thr) n.2120T>C c.449T>C (p.Met150Thr) c.1643T>C (p.Met548Thr) | gnomAD v4 |
| 9 | g.91724842A>T | CA373797855 | ROR2 | c.1652T>A (p.Met551Lys) c.1232T>A (p.Met411Lys) n.2120T>A c.449T>A (p.Met150Lys) c.1643T>A (p.Met548Lys) | |
| 9 | g.91724843T>A | CA373797858 | ROR2 | c.1651A>T (p.Met551Leu) c.1231A>T (p.Met411Leu) n.2119A>T c.448A>T (p.Met150Leu) c.1642A>T (p.Met548Leu) | |
| 9 | g.91724843T>C | CA373797856 | ROR2 | c.1651A>G (p.Met551Val) c.1231A>G (p.Met411Val) n.2119A>G c.448A>G (p.Met150Val) c.1642A>G (p.Met548Val) | |
| 9 | g.91724843T>G | CA373797857 | ROR2 | c.1651A>C (p.Met551Leu) c.1231A>C (p.Met411Leu) n.2119A>C c.448A>C (p.Met150Leu) c.1642A>C (p.Met548Leu) | |
| 9 | g.91724844G>A | CA466339248 | ROR2 | c.1650C>T (p.Ser550=) c.1230C>T (p.Ser410=) n.2118C>T c.447C>T (p.Ser149=) c.1641C>T (p.Ser547=) | |
| 9 | g.91724844G>C | CA373797859 | ROR2 | c.1650C>G (p.Ser550Arg) c.1230C>G (p.Ser410Arg) n.2118C>G c.447C>G (p.Ser149Arg) c.1641C>G (p.Ser547Arg) | |
| 9 | g.91724844G>T | CA373797860 | ROR2 | c.1650C>A (p.Ser550Arg) c.1230C>A (p.Ser410Arg) n.2118C>A c.447C>A (p.Ser149Arg) c.1641C>A (p.Ser547Arg) | |
| 9 | g.91724845C>A | CA373797861 | ROR2 | c.1649G>T (p.Ser550Ile) c.1229G>T (p.Ser410Ile) n.2117G>T c.446G>T (p.Ser149Ile) c.1640G>T (p.Ser547Ile) | gnomAD v4 |
| 9 | g.91724845C= | CA1863923345 | ROR2 | c.1649G= (p.Ser550=) c.1229G= (p.Ser410=) n.2117G= c.446G= (p.Ser149=) c.1640G= (p.Ser547=) | |
| 9 | g.91724845C>G | CA373797862 | ROR2 | c.1649G>C (p.Ser550Thr) c.1229G>C (p.Ser410Thr) n.2117G>C c.446G>C (p.Ser149Thr) c.1640G>C (p.Ser547Thr) | |
| 9 | g.91724845C>T | CA373797863 | ROR2 | c.1649G>A (p.Ser550Asn) c.1229G>A (p.Ser410Asn) n.2117G>A c.446G>A (p.Ser149Asn) c.1640G>A (p.Ser547Asn) | dbSNP gnomAD v2 gnomAD v4 |
| 9 | g.91724846T>A | CA373797864 | ROR2 | c.1648A>T (p.Ser550Cys) c.1228A>T (p.Ser410Cys) n.2116A>T c.445A>T (p.Ser149Cys) c.1639A>T (p.Ser547Cys) | gnomAD v4 |
| 9 | g.91724846T>C | CA373797865 | ROR2 | c.1648A>G (p.Ser550Gly) c.1228A>G (p.Ser410Gly) n.2116A>G c.445A>G (p.Ser149Gly) c.1639A>G (p.Ser547Gly) | |
| 9 | g.91724846T>G | CA373797866 | ROR2 | c.1648A>C (p.Ser550Arg) c.1228A>C (p.Ser410Arg) n.2116A>C c.445A>C (p.Ser149Arg) c.1639A>C (p.Ser547Arg) | |
| 9 | g.91724847C>A | CA466339251 | ROR2 | c.1647G>T (p.Leu549=) c.1227G>T (p.Leu409=) n.2115G>T c.444G>T (p.Leu148=) c.1638G>T (p.Leu546=) | gnomAD v4 |
| 9 | g.91724847C= | CA1863923347 | ROR2 | c.1647G= (p.Leu549=) c.1227G= (p.Leu409=) n.2115G= c.444G= (p.Leu148=) c.1638G= (p.Leu546=) | |
| 9 | g.91724847C>G | CA466339252 | ROR2 | c.1647G>C (p.Leu549=) c.1227G>C (p.Leu409=) n.2115G>C c.444G>C (p.Leu148=) c.1638G>C (p.Leu546=) | dbSNP gnomAD v4 |
| 9 | g.91724847C>T | CA5120622 | ROR2 | c.1647G>A (p.Leu549=) c.1227G>A (p.Leu409=) n.2115G>A c.444G>A (p.Leu148=) c.1638G>A (p.Leu546=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 9 | g.91724848del | CA2690633157 | ROR2 | c.1646del (p.Leu549ArgfsTer3) c.1226del (p.Leu409ArgfsTer3) n.2114del c.443del (p.Leu148ArgfsTer3) c.1637del (p.Leu546ArgfsTer3) | gnomAD v4 |
| 9 | g.91724848A= | CA1863923348 | ROR2 | c.1646T= (p.Leu549=) c.1226T= (p.Leu409=) n.2114T= c.443T= (p.Leu148=) c.1637T= (p.Leu546=) | |
| 9 | g.91724848A>C | CA373797867 | ROR2 | c.1646T>G (p.Leu549Arg) c.1226T>G (p.Leu409Arg) n.2114T>G c.443T>G (p.Leu148Arg) c.1637T>G (p.Leu546Arg) | |
| 9 | g.91724848A>G | CA5120623 | ROR2 | c.1646T>C (p.Leu549Pro) c.1226T>C (p.Leu409Pro) n.2114T>C c.443T>C (p.Leu148Pro) c.1637T>C (p.Leu546Pro) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 9 | g.91724848A>T | CA373797868 | ROR2 | c.1646T>A (p.Leu549Gln) c.1226T>A (p.Leu409Gln) n.2114T>A c.443T>A (p.Leu148Gln) c.1637T>A (p.Leu546Gln) | |
| 9 | g.91724849G>A | CA466339254 | ROR2 | c.1645C>T (p.Leu549=) c.1225C>T (p.Leu409=) n.2113C>T c.442C>T (p.Leu148=) c.1636C>T (p.Leu546=) | |
| 9 | g.91724849G>C | CA373797870 | ROR2 | c.1645C>G (p.Leu549Val) c.1225C>G (p.Leu409Val) n.2113C>G c.442C>G (p.Leu148Val) c.1636C>G (p.Leu546Val) | |
| 9 | g.91724849G>T | CA373797869 | ROR2 | c.1645C>A (p.Leu549Met) c.1225C>A (p.Leu409Met) n.2113C>A c.442C>A (p.Leu148Met) c.1636C>A (p.Leu546Met) | |
| 9 | g.91724850G>A | CA466339256 | ROR2 | c.1644C>T (p.Pro548=) c.1224C>T (p.Pro408=) n.2112C>T c.441C>T (p.Pro147=) c.1635C>T (p.Pro545=) | |
| 9 | g.91724850G>C | CA466339257 | ROR2 | c.1644C>G (p.Pro548=) c.1224C>G (p.Pro408=) n.2112C>G c.441C>G (p.Pro147=) c.1635C>G (p.Pro545=) | |
| 9 | g.91724850G= | CA1863923350 | ROR2 | c.1644C= (p.Pro548=) c.1224C= (p.Pro408=) n.2112C= c.441C= (p.Pro147=) c.1635C= (p.Pro545=) | |
| 9 | g.91724850G>T | CA466339258 | ROR2 | c.1644C>A (p.Pro548=) c.1224C>A (p.Pro408=) n.2112C>A c.441C>A (p.Pro147=) c.1635C>A (p.Pro545=) | ClinVar dbSNP |
| 9 | g.91724851G>A | CA373797871 | ROR2 | c.1643C>T (p.Pro548Leu) c.1223C>T (p.Pro408Leu) n.2111C>T c.440C>T (p.Pro147Leu) c.1634C>T (p.Pro545Leu) | dbSNP gnomAD v4 |
| 9 | g.91724851G>C | CA373797872 | ROR2 | c.1643C>G (p.Pro548Arg) c.1223C>G (p.Pro408Arg) n.2111C>G c.440C>G (p.Pro147Arg) c.1634C>G (p.Pro545Arg) | dbSNP |
| 9 | g.91724851G= | CA1863923351 | ROR2 | c.1643C= (p.Pro548=) c.1223C= (p.Pro408=) n.2111C= c.440C= (p.Pro147=) c.1634C= (p.Pro545=) | |
| 9 | g.91724851G>T | CA373797873 | ROR2 | c.1643C>A (p.Pro548His) c.1223C>A (p.Pro408His) n.2111C>A c.440C>A (p.Pro147His) c.1634C>A (p.Pro545His) | |
| 9 | g.91724852G>A | CA5120624 | ROR2 | c.1642C>T (p.Pro548Ser) c.1222C>T (p.Pro408Ser) n.2110C>T c.439C>T (p.Pro147Ser) c.1633C>T (p.Pro545Ser) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 9 | g.91724852G>C | CA373797874 | ROR2 | c.1642C>G (p.Pro548Ala) c.1222C>G (p.Pro408Ala) n.2110C>G c.439C>G (p.Pro147Ala) c.1633C>G (p.Pro545Ala) | |
| 9 | g.91724852G= | CA1863923354 | ROR2 | c.1642C= (p.Pro548=) c.1222C= (p.Pro408=) n.2110C= c.439C= (p.Pro147=) c.1633C= (p.Pro545=) | |
| 9 | g.91724852G>T | CA373797875 | ROR2 | c.1642C>A (p.Pro548Thr) c.1222C>A (p.Pro408Thr) n.2110C>A c.439C>A (p.Pro147Thr) c.1633C>A (p.Pro545Thr) | dbSNP gnomAD v2 gnomAD v4 |
| 9 | g.91724853C>A | CA373797876 | ROR2 | c.1641G>T (p.Gln547His) c.1221G>T (p.Gln407His) n.2109G>T c.438G>T (p.Gln146His) c.1632G>T (p.Gln544His) | |
| 9 | g.91724853C>G | CA373797877 | ROR2 | c.1641G>C (p.Gln547His) c.1221G>C (p.Gln407His) n.2109G>C c.438G>C (p.Gln146His) c.1632G>C (p.Gln544His) | |
| 9 | g.91724853C>T | CA466339260 | ROR2 | c.1641G>A (p.Gln547=) c.1221G>A (p.Gln407=) n.2109G>A c.438G>A (p.Gln146=) c.1632G>A (p.Gln544=) | |
| 9 | g.91724854T>A | CA373797878 | ROR2 | c.1640A>T (p.Gln547Leu) c.1220A>T (p.Gln407Leu) n.2108A>T c.437A>T (p.Gln146Leu) c.1631A>T (p.Gln544Leu) | |
| 9 | g.91724854T>C | CA373797879 | ROR2 | c.1640A>G (p.Gln547Arg) c.1220A>G (p.Gln407Arg) n.2108A>G c.437A>G (p.Gln146Arg) c.1631A>G (p.Gln544Arg) | |
| 9 | g.91724854T>G | CA373797880 | ROR2 | c.1640A>C (p.Gln547Pro) c.1220A>C (p.Gln407Pro) n.2108A>C c.437A>C (p.Gln146Pro) c.1631A>C (p.Gln544Pro) | |
| 9 | g.91724855G>A | CA373797881 | ROR2 | c.1639C>T (p.Gln547Ter) c.1219C>T (p.Gln407Ter) n.2107C>T c.436C>T (p.Gln146Ter) c.1630C>T (p.Gln544Ter) | dbSNP |
| 9 | g.91724855G>C | CA373797882 | ROR2 | c.1639C>G (p.Gln547Glu) c.1219C>G (p.Gln407Glu) n.2107C>G c.436C>G (p.Gln146Glu) c.1630C>G (p.Gln544Glu) | |
| 9 | g.91724855G= | CA1863923356 | ROR2 | c.1639C= (p.Gln547=) c.1219C= (p.Gln407=) n.2107C= c.436C= (p.Gln146=) c.1630C= (p.Gln544=) | |
| 9 | g.91724855G>T | CA373797883 | ROR2 | c.1639C>A (p.Gln547Lys) c.1219C>A (p.Gln407Lys) n.2107C>A c.436C>A (p.Gln146Lys) c.1630C>A (p.Gln544Lys) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 9 | g.91724856G>A | CA466339264 | ROR2 | c.1638C>T (p.Asp546=) c.1218C>T (p.Asp406=) n.2106C>T c.435C>T (p.Asp145=) c.1629C>T (p.Asp543=) | gnomAD v4 |
| 9 | g.91724856G>C | CA373797885 | ROR2 | c.1638C>G (p.Asp546Glu) c.1218C>G (p.Asp406Glu) n.2106C>G c.435C>G (p.Asp145Glu) c.1629C>G (p.Asp543Glu) | |
| 9 | g.91724856G>T | CA373797884 | ROR2 | c.1638C>A (p.Asp546Glu) c.1218C>A (p.Asp406Glu) n.2106C>A c.435C>A (p.Asp145Glu) c.1629C>A (p.Asp543Glu) | |
| 9 | g.91724857T>A | CA373797886 | ROR2 | c.1637A>T (p.Asp546Val) c.1217A>T (p.Asp406Val) n.2105A>T c.434A>T (p.Asp145Val) c.1628A>T (p.Asp543Val) | |
| 9 | g.91724857T>C | CA373797887 | ROR2 | c.1637A>G (p.Asp546Gly) c.1217A>G (p.Asp406Gly) n.2105A>G c.434A>G (p.Asp145Gly) c.1628A>G (p.Asp543Gly) | COSMIC |
| 9 | g.91724857T>G | CA373797888 | ROR2 | c.1637A>C (p.Asp546Ala) c.1217A>C (p.Asp406Ala) n.2105A>C c.434A>C (p.Asp145Ala) c.1628A>C (p.Asp543Ala) | |
| 9 | g.91724858C>A | CA373797889 | ROR2 | c.1636G>T (p.Asp546Tyr) c.1216G>T (p.Asp406Tyr) n.2104G>T c.433G>T (p.Asp145Tyr) c.1627G>T (p.Asp543Tyr) | |
| 9 | g.91724858C= | CA1863923359 | ROR2 | c.1636G= (p.Asp546=) c.1216G= (p.Asp406=) n.2104G= c.433G= (p.Asp145=) c.1627G= (p.Asp543=) | |
| 9 | g.91724858C>G | CA373797890 | ROR2 | c.1636G>C (p.Asp546His) c.1216G>C (p.Asp406His) n.2104G>C c.433G>C (p.Asp145His) c.1627G>C (p.Asp543His) | |
| 9 | g.91724858C>T | CA373797891 | ROR2 | c.1636G>A (p.Asp546Asn) c.1216G>A (p.Asp406Asn) n.2104G>A c.433G>A (p.Asp145Asn) c.1627G>A (p.Asp543Asn) | dbSNP gnomAD v4 |
| 9 | g.91724859C>A | CA373797893 | ROR2 | c.1635G>T (p.Lys545Asn) c.1215G>T (p.Lys405Asn) n.2103G>T c.432G>T (p.Lys144Asn) c.1626G>T (p.Lys542Asn) | COSMIC |
| 9 | g.91724859C= | CA1863923360 | ROR2 | c.1635G= (p.Lys545=) c.1215G= (p.Lys405=) n.2103G= c.432G= (p.Lys144=) c.1626G= (p.Lys542=) | |
| 9 | g.91724859C>G | CA373797892 | ROR2 | c.1635G>C (p.Lys545Asn) c.1215G>C (p.Lys405Asn) n.2103G>C c.432G>C (p.Lys144Asn) c.1626G>C (p.Lys542Asn) | |
| 9 | g.91724859C>T | CA466339266 | ROR2 | c.1635G>A (p.Lys545=) c.1215G>A (p.Lys405=) n.2103G>A c.432G>A (p.Lys144=) c.1626G>A (p.Lys542=) | dbSNP |
| 9 | g.91724860T>A | CA373797894 | ROR2 | c.1634A>T (p.Lys545Met) c.1214A>T (p.Lys405Met) n.2102A>T c.431A>T (p.Lys144Met) c.1625A>T (p.Lys542Met) | |
| 9 | g.91724860T>C | CA373797895 | ROR2 | c.1634A>G (p.Lys545Arg) c.1214A>G (p.Lys405Arg) n.2102A>G c.431A>G (p.Lys144Arg) c.1625A>G (p.Lys542Arg) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 9 | g.91724860T>G | CA373797896 | ROR2 | c.1634A>C (p.Lys545Thr) c.1214A>C (p.Lys405Thr) n.2102A>C c.431A>C (p.Lys144Thr) c.1625A>C (p.Lys542Thr) | |
| 9 | g.91724860T= | CA1863923362 | ROR2 | c.1634A= (p.Lys545=) c.1214A= (p.Lys405=) n.2102A= c.431A= (p.Lys144=) c.1625A= (p.Lys542=) | |
| 9 | g.91724861T>A | CA373797897 | ROR2 | c.1633A>T (p.Lys545Ter) c.1213A>T (p.Lys405Ter) n.2101A>T c.430A>T (p.Lys144Ter) c.1624A>T (p.Lys542Ter) | |
| 9 | g.91724861T>C | CA373797898 | ROR2 | c.1633A>G (p.Lys545Glu) c.1213A>G (p.Lys405Glu) n.2101A>G c.430A>G (p.Lys144Glu) c.1624A>G (p.Lys542Glu) | |
| 9 | g.91724861T>G | CA373797899 | ROR2 | c.1633A>C (p.Lys545Gln) c.1213A>C (p.Lys405Gln) n.2101A>C c.430A>C (p.Lys144Gln) c.1624A>C (p.Lys542Gln) | |
| 9 | g.91724862G>A | CA466339270 | ROR2 | c.1632C>T (p.Thr544=) c.1212C>T (p.Thr404=) n.2100C>T c.429C>T (p.Thr143=) c.1623C>T (p.Thr541=) | |
| 9 | g.91724862G>C | CA466339271 | ROR2 | c.1632C>G (p.Thr544=) c.1212C>G (p.Thr404=) n.2100C>G c.429C>G (p.Thr143=) c.1623C>G (p.Thr541=) | |
| 9 | g.91724862G>T | CA466339272 | ROR2 | c.1632C>A (p.Thr544=) c.1212C>A (p.Thr404=) n.2100C>A c.429C>A (p.Thr143=) c.1623C>A (p.Thr541=) | gnomAD v4 |
| 9 | g.91724863G>A | CA373797901 | ROR2 | c.1631C>T (p.Thr544Ile) c.1211C>T (p.Thr404Ile) n.2099C>T c.428C>T (p.Thr143Ile) c.1622C>T (p.Thr541Ile) | gnomAD v4 |
| 9 | g.91724863G>C | CA373797905 | ROR2 | c.1631C>G (p.Thr544Ser) c.1211C>G (p.Thr404Ser) n.2099C>G c.428C>G (p.Thr143Ser) c.1622C>G (p.Thr541Ser) | |
| 9 | g.91724863G>T | CA373797903 | ROR2 | c.1631C>A (p.Thr544Asn) c.1211C>A (p.Thr404Asn) n.2099C>A c.428C>A (p.Thr143Asn) c.1622C>A (p.Thr541Asn) | |
| 9 | g.91724864T>A | CA373797907 | ROR2 | c.1630A>T (p.Thr544Ser) c.1210A>T (p.Thr404Ser) n.2098A>T c.427A>T (p.Thr143Ser) c.1621A>T (p.Thr541Ser) | |
| 9 | g.91724864T>C | CA5120625 | ROR2 | c.1630A>G (p.Thr544Ala) c.1210A>G (p.Thr404Ala) n.2098A>G c.427A>G (p.Thr143Ala) c.1621A>G (p.Thr541Ala) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 9 | g.91724864T>G | CA373797908 | ROR2 | c.1630A>C (p.Thr544Pro) c.1210A>C (p.Thr404Pro) n.2098A>C c.427A>C (p.Thr143Pro) c.1621A>C (p.Thr541Pro) | dbSNP |
| 9 | g.91724864T= | CA1863923364 | ROR2 | c.1630A= (p.Thr544=) c.1210A= (p.Thr404=) n.2098A= c.427A= (p.Thr143=) c.1621A= (p.Thr541=) | |
| 9 | g.91724865C>A | CA466339275 | ROR2 | c.1629G>T (p.Val543=) c.1209G>T (p.Val403=) n.2097G>T c.426G>T (p.Val142=) c.1620G>T (p.Val540=) | |
| 9 | g.91724865C>G | CA466339277 | ROR2 | c.1629G>C (p.Val543=) c.1209G>C (p.Val403=) n.2097G>C c.426G>C (p.Val142=) c.1620G>C (p.Val540=) | |
| 9 | g.91724865C>T | CA466339276 | ROR2 | c.1629G>A (p.Val543=) c.1209G>A (p.Val403=) n.2097G>A c.426G>A (p.Val142=) c.1620G>A (p.Val540=) | |
| 9 | g.91724866A= | CA1863923367 | ROR2 | c.1628T= (p.Val543=) c.1208T= (p.Val403=) n.2096T= c.425T= (p.Val142=) c.1619T= (p.Val540=) | |
| 9 | g.91724866A>C | CA373797911 | ROR2 | c.1628T>G (p.Val543Gly) c.1208T>G (p.Val403Gly) n.2096T>G c.425T>G (p.Val142Gly) c.1619T>G (p.Val540Gly) | |
| 9 | g.91724866A>G | CA373797912 | ROR2 | c.1628T>C (p.Val543Ala) c.1208T>C (p.Val403Ala) n.2096T>C c.425T>C (p.Val142Ala) c.1619T>C (p.Val540Ala) | dbSNP gnomAD v2 gnomAD v4 |
| 9 | g.91724866A>T | CA373797914 | ROR2 | c.1628T>A (p.Val543Glu) c.1208T>A (p.Val403Glu) n.2096T>A c.425T>A (p.Val142Glu) c.1619T>A (p.Val540Glu) | |
| 9 | g.91724867C>A | CA373797916 | ROR2 | c.1627G>T (p.Val543Leu) c.1207G>T (p.Val403Leu) n.2095G>T c.424G>T (p.Val142Leu) c.1618G>T (p.Val540Leu) | |
| 9 | g.91724867C>G | CA373797918 | ROR2 | c.1627G>C (p.Val543Leu) c.1207G>C (p.Val403Leu) n.2095G>C c.424G>C (p.Val142Leu) c.1618G>C (p.Val540Leu) | |
| 9 | g.91724867C>T | CA373797919 | ROR2 | c.1627G>A (p.Val543Met) c.1207G>A (p.Val403Met) n.2095G>A c.424G>A (p.Val142Met) c.1618G>A (p.Val540Met) | |
| 9 | g.91724868C>A | CA466339281 | ROR2 | c.1626G>T (p.Val542=) c.1206G>T (p.Val402=) n.2094G>T c.423G>T (p.Val141=) c.1617G>T (p.Val539=) | |
| 9 | g.91724868C>G | CA466339282 | ROR2 | c.1626G>C (p.Val542=) c.1206G>C (p.Val402=) n.2094G>C c.423G>C (p.Val141=) c.1617G>C (p.Val539=) | |
| 9 | g.91724868C>T | CA466339283 | ROR2 | c.1626G>A (p.Val542=) c.1206G>A (p.Val402=) n.2094G>A c.423G>A (p.Val141=) c.1617G>A (p.Val539=) | |
| 9 | g.91724869A= | CA1863923369 | ROR2 | c.1625T= (p.Val542=) c.1205T= (p.Val402=) n.2093T= c.422T= (p.Val141=) c.1616T= (p.Val539=) | |
| 9 | g.91724869A>C | CA373797921 | ROR2 | c.1625T>G (p.Val542Gly) c.1205T>G (p.Val402Gly) n.2093T>G c.422T>G (p.Val141Gly) c.1616T>G (p.Val539Gly) | |
| 9 | g.91724869A>G | CA373797923 | ROR2 | c.1625T>C (p.Val542Ala) c.1205T>C (p.Val402Ala) n.2093T>C c.422T>C (p.Val141Ala) c.1616T>C (p.Val539Ala) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 9 | g.91724869A>T | CA373797924 | ROR2 | c.1625T>A (p.Val542Glu) c.1205T>A (p.Val402Glu) n.2093T>A c.422T>A (p.Val141Glu) c.1616T>A (p.Val539Glu) | |
| 9 | g.91724870C>A | CA5120627 | ROR2 | c.1624G>T (p.Val542Leu) c.1204G>T (p.Val402Leu) n.2092G>T c.421G>T (p.Val141Leu) c.1615G>T (p.Val539Leu) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 9 | g.91724870C= | CA1863923371 | ROR2 | c.1624G= (p.Val542=) c.1204G= (p.Val402=) n.2092G= c.421G= (p.Val141=) c.1615G= (p.Val539=) | |
| 9 | g.91724870C>G | CA373797926 | ROR2 | c.1624G>C (p.Val542Leu) c.1204G>C (p.Val402Leu) n.2092G>C c.421G>C (p.Val141Leu) c.1615G>C (p.Val539Leu) | |
| 9 | g.91724870C>T | CA5120626 | ROR2 | c.1624G>A (p.Val542Met) c.1204G>A (p.Val402Met) n.2092G>A c.421G>A (p.Val141Met) c.1615G>A (p.Val539Met) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 9 | g.91724871G>A | CA5120628 | ROR2 | c.1623C>T (p.Gly541=) c.1203C>T (p.Gly401=) n.2091C>T c.420C>T (p.Gly140=) c.1614C>T (p.Gly538=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 9 | g.91724871G>C | CA466339288 | ROR2 | c.1623C>G (p.Gly541=) c.1203C>G (p.Gly401=) n.2091C>G c.420C>G (p.Gly140=) c.1614C>G (p.Gly538=) | |
| 9 | g.91724871G= | CA1863923374 | ROR2 | c.1623C= (p.Gly541=) c.1203C= (p.Gly401=) n.2091C= c.420C= (p.Gly140=) c.1614C= (p.Gly538=) | |
| 9 | g.91724871G>T | CA466339289 | ROR2 | c.1623C>A (p.Gly541=) c.1203C>A (p.Gly401=) n.2091C>A c.420C>A (p.Gly140=) c.1614C>A (p.Gly538=) | gnomAD v4 |
| 9 | g.91724872C>A | CA373797929 | ROR2 | c.1622G>T (p.Gly541Val) c.1202G>T (p.Gly401Val) n.2090G>T c.419G>T (p.Gly140Val) c.1613G>T (p.Gly538Val) | |
| 9 | g.91724872C>G | CA373797932 | ROR2 | c.1622G>C (p.Gly541Ala) c.1202G>C (p.Gly401Ala) n.2090G>C c.419G>C (p.Gly140Ala) c.1613G>C (p.Gly538Ala) | |
| 9 | g.91724872C>T | CA373797931 | ROR2 | c.1622G>A (p.Gly541Asp) c.1202G>A (p.Gly401Asp) n.2090G>A c.419G>A (p.Gly140Asp) c.1613G>A (p.Gly538Asp) | |
| 9 | g.91724873C>A | CA373797934 | ROR2 | c.1621G>T (p.Gly541Cys) c.1201G>T (p.Gly401Cys) n.2089G>T c.418G>T (p.Gly140Cys) c.1612G>T (p.Gly538Cys) | |
| 9 | g.91724873C= | CA1863923376 | ROR2 | c.1621G= (p.Gly541=) c.1201G= (p.Gly401=) n.2089G= c.418G= (p.Gly140=) c.1612G= (p.Gly538=) | |
| 9 | g.91724873C>G | CA373797935 | ROR2 | c.1621G>C (p.Gly541Arg) c.1201G>C (p.Gly401Arg) n.2089G>C c.418G>C (p.Gly140Arg) c.1612G>C (p.Gly538Arg) | |
| 9 | g.91724873C>T | CA373797937 | ROR2 | c.1621G>A (p.Gly541Ser) c.1201G>A (p.Gly401Ser) n.2089G>A c.418G>A (p.Gly140Ser) c.1612G>A (p.Gly538Ser) | dbSNP |
| 9 | g.91724874C>A | CA466339294 | ROR2 | c.1620G>T (p.Leu540=) c.1200G>T (p.Leu400=) n.2088G>T c.417G>T (p.Leu139=) c.1611G>T (p.Leu537=) | |
| 9 | g.91724874C>G | CA466339292 | ROR2 | c.1620G>C (p.Leu540=) c.1200G>C (p.Leu400=) n.2088G>C c.417G>C (p.Leu139=) c.1611G>C (p.Leu537=) | |
| 9 | g.91724874C>T | CA466339293 | ROR2 | c.1620G>A (p.Leu540=) c.1200G>A (p.Leu400=) n.2088G>A c.417G>A (p.Leu139=) c.1611G>A (p.Leu537=) | |
| 9 | g.91724875A>C | CA373797939 | ROR2 | c.1619T>G (p.Leu540Arg) c.1199T>G (p.Leu400Arg) n.2087T>G c.416T>G (p.Leu139Arg) c.1610T>G (p.Leu537Arg) | |
| 9 | g.91724875A>G | CA373797940 | ROR2 | c.1619T>C (p.Leu540Pro) c.1199T>C (p.Leu400Pro) n.2087T>C c.416T>C (p.Leu139Pro) c.1610T>C (p.Leu537Pro) | |
| 9 | g.91724875A>T | CA373797941 | ROR2 | c.1619T>A (p.Leu540Gln) c.1199T>A (p.Leu400Gln) n.2087T>A c.416T>A (p.Leu139Gln) c.1610T>A (p.Leu537Gln) | |
| 9 | g.91724876G>A | CA466339297 | ROR2 | c.1618C>T (p.Leu540=) c.1198C>T (p.Leu400=) n.2086C>T c.415C>T (p.Leu139=) c.1609C>T (p.Leu537=) | |
| 9 | g.91724876G>C | CA373797943 | ROR2 | c.1618C>G (p.Leu540Val) c.1198C>G (p.Leu400Val) n.2086C>G c.415C>G (p.Leu139Val) c.1609C>G (p.Leu537Val) | |
| 9 | g.91724876G>T | CA373797945 | ROR2 | c.1618C>A (p.Leu540Met) c.1198C>A (p.Leu400Met) n.2086C>A c.415C>A (p.Leu139Met) c.1609C>A (p.Leu537Met) | |
| 9 | g.91724876_91724877insA | CA2785076922 | ROR2 | c.1617_1618insT (p.Leu540SerfsTer?) c.1197_1198insT (p.Leu400SerfsTer?) n.2085_2086insT c.414_415insT (p.Leu139SerfsTer?) c.1608_1609insT (p.Leu537SerfsTer?) | |
| 9 | g.91724877C>A | CA466339299 | ROR2 | c.1617G>T (p.Leu539=) c.1197G>T (p.Leu399=) n.2085G>T c.414G>T (p.Leu138=) c.1608G>T (p.Leu536=) | gnomAD v4 |
| 9 | g.91724877C= | CA1863923378 | ROR2 | c.1617G= (p.Leu539=) c.1197G= (p.Leu399=) n.2085G= c.414G= (p.Leu138=) c.1608G= (p.Leu536=) | |
| 9 | g.91724877C>G | CA466339300 | ROR2 | c.1617G>C (p.Leu539=) c.1197G>C (p.Leu399=) n.2085G>C c.414G>C (p.Leu138=) c.1608G>C (p.Leu536=) | gnomAD v4 |
| 9 | g.91724877C>T | CA466339302 | ROR2 | c.1617G>A (p.Leu539=) c.1197G>A (p.Leu399=) n.2085G>A c.414G>A (p.Leu138=) c.1608G>A (p.Leu536=) | dbSNP gnomAD v3 gnomAD v4 |
| 9 | g.91724878A>C | CA373797947 | ROR2 | c.1616T>G (p.Leu539Arg) c.1196T>G (p.Leu399Arg) n.2084T>G c.413T>G (p.Leu138Arg) c.1607T>G (p.Leu536Arg) | |
| 9 | g.91724878A>G | CA373797948 | ROR2 | c.1616T>C (p.Leu539Pro) c.1196T>C (p.Leu399Pro) n.2084T>C c.413T>C (p.Leu138Pro) c.1607T>C (p.Leu536Pro) | |
| 9 | g.91724878A>T | CA373797950 | ROR2 | c.1616T>A (p.Leu539Gln) c.1196T>A (p.Leu399Gln) n.2084T>A c.413T>A (p.Leu138Gln) c.1607T>A (p.Leu536Gln) | |
| 9 | g.91724879G>A | CA466339304 | ROR2 | c.1615C>T (p.Leu539=) c.1195C>T (p.Leu399=) n.2083C>T c.412C>T (p.Leu138=) c.1606C>T (p.Leu536=) | |
| 9 | g.91724879G>C | CA373797952 | ROR2 | c.1615C>G (p.Leu539Val) c.1195C>G (p.Leu399Val) n.2083C>G c.412C>G (p.Leu138Val) c.1606C>G (p.Leu536Val) | |
| 9 | g.91724879G>T | CA373797953 | ROR2 | c.1615C>A (p.Leu539Met) c.1195C>A (p.Leu399Met) n.2083C>A c.412C>A (p.Leu138Met) c.1606C>A (p.Leu536Met) | |
| 9 | g.91724880G>A | CA466339305 | ROR2 | c.1614C>T (p.Cys538=) c.1194C>T (p.Cys398=) n.2082C>T c.411C>T (p.Cys137=) c.1605C>T (p.Cys535=) | gnomAD v4 COSMIC |
| 9 | g.91724880G>C | CA373797955 | ROR2 | c.1614C>G (p.Cys538Trp) c.1194C>G (p.Cys398Trp) n.2082C>G c.411C>G (p.Cys137Trp) c.1605C>G (p.Cys535Trp) | |
| 9 | g.91724880G>T | CA373797956 | ROR2 | c.1614C>A (p.Cys538Ter) c.1194C>A (p.Cys398Ter) n.2082C>A c.411C>A (p.Cys137Ter) c.1605C>A (p.Cys535Ter) | gnomAD v4 |
| 9 | g.91724881C>A | CA373797959 | ROR2 | c.1613G>T (p.Cys538Phe) c.1193G>T (p.Cys398Phe) n.2081G>T c.410G>T (p.Cys137Phe) c.1604G>T (p.Cys535Phe) | dbSNP gnomAD v4 |
| 9 | g.91724881C= | CA1863923380 | ROR2 | c.1613G= (p.Cys538=) c.1193G= (p.Cys398=) n.2081G= c.410G= (p.Cys137=) c.1604G= (p.Cys535=) | |
| 9 | g.91724881C>G | CA373797960 | ROR2 | c.1613G>C (p.Cys538Ser) c.1193G>C (p.Cys398Ser) n.2081G>C c.410G>C (p.Cys137Ser) c.1604G>C (p.Cys535Ser) | |
| 9 | g.91724881C>T | CA373797961 | ROR2 | c.1613G>A (p.Cys538Tyr) c.1193G>A (p.Cys398Tyr) n.2081G>A c.410G>A (p.Cys137Tyr) c.1604G>A (p.Cys535Tyr) | |
| 9 | g.91724882A= | CA1863923382 | ROR2 | c.1612T= (p.Cys538=) c.1192T= (p.Cys398=) n.2080T= c.409T= (p.Cys137=) c.1603T= (p.Cys535=) | |
| 9 | g.91724882A>C | CA373797963 | ROR2 | c.1612T>G (p.Cys538Gly) c.1192T>G (p.Cys398Gly) n.2080T>G c.409T>G (p.Cys137Gly) c.1603T>G (p.Cys535Gly) | |
| 9 | g.91724882A>G | CA373797964 | ROR2 | c.1612T>C (p.Cys538Arg) c.1192T>C (p.Cys398Arg) n.2080T>C c.409T>C (p.Cys137Arg) c.1603T>C (p.Cys535Arg) | dbSNP |
| 9 | g.91724882A>T | CA373797966 | ROR2 | c.1612T>A (p.Cys538Ser) c.1192T>A (p.Cys398Ser) n.2080T>A c.409T>A (p.Cys137Ser) c.1603T>A (p.Cys535Ser) | |
| 9 | g.91724883G>A | CA466339309 | ROR2 | c.1611C>T (p.Val537=) c.1191C>T (p.Val397=) n.2079C>T c.408C>T (p.Val136=) c.1602C>T (p.Val534=) | gnomAD v4 |
| 9 | g.91724883G>C | CA466339310 | ROR2 | c.1611C>G (p.Val537=) c.1191C>G (p.Val397=) n.2079C>G c.408C>G (p.Val136=) c.1602C>G (p.Val534=) | |
| 9 | g.91724883G>T | CA466339311 | ROR2 | c.1611C>A (p.Val537=) c.1191C>A (p.Val397=) n.2079C>A c.408C>A (p.Val136=) c.1602C>A (p.Val534=) | gnomAD v4 |
| 9 | g.91724884A>C | CA373797967 | ROR2 | c.1610T>G (p.Val537Gly) c.1190T>G (p.Val397Gly) n.2078T>G c.407T>G (p.Val136Gly) c.1601T>G (p.Val534Gly) | |
| 9 | g.91724884A>G | CA373797968 | ROR2 | c.1610T>C (p.Val537Ala) c.1190T>C (p.Val397Ala) n.2078T>C c.407T>C (p.Val136Ala) c.1601T>C (p.Val534Ala) | |
| 9 | g.91724884A>T | CA373797970 | ROR2 | c.1610T>A (p.Val537Asp) c.1190T>A (p.Val397Asp) n.2078T>A c.407T>A (p.Val136Asp) c.1601T>A (p.Val534Asp) | |
| 9 | g.91724885C>A | CA373797972 | ROR2 | c.1609G>T (p.Val537Phe) c.1189G>T (p.Val397Phe) n.2077G>T c.406G>T (p.Val136Phe) c.1600G>T (p.Val534Phe) | gnomAD v4 |
| 9 | g.91724885C= | CA1863923384 | ROR2 | c.1609G= (p.Val537=) c.1189G= (p.Val397=) n.2077G= c.406G= (p.Val136=) c.1600G= (p.Val534=) | |
| 9 | g.91724885C>G | CA5120629 | ROR2 | c.1609G>C (p.Val537Leu) c.1189G>C (p.Val397Leu) n.2077G>C c.406G>C (p.Val136Leu) c.1600G>C (p.Val534Leu) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 9 | g.91724885C>T | CA5120630 | ROR2 | c.1609G>A (p.Val537Ile) c.1189G>A (p.Val397Ile) n.2077G>A c.406G>A (p.Val136Ile) c.1600G>A (p.Val534Ile) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 9 | g.91724886G>A | CA5120631 | ROR2 | c.1608C>T (p.Val536=) c.1188C>T (p.Val396=) n.2076C>T c.405C>T (p.Val135=) c.1599C>T (p.Val533=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 9 | g.91724886G>C | CA466339314 | ROR2 | c.1608C>G (p.Val536=) c.1188C>G (p.Val396=) n.2076C>G c.405C>G (p.Val135=) c.1599C>G (p.Val533=) | |
| 9 | g.91724886G= | CA1863923387 | ROR2 | c.1608C= (p.Val536=) c.1188C= (p.Val396=) n.2076C= c.405C= (p.Val135=) c.1599C= (p.Val533=) | |
| 9 | g.91724886G>T | CA466339316 | ROR2 | c.1608C>A (p.Val536=) c.1188C>A (p.Val396=) n.2076C>A c.405C>A (p.Val135=) c.1599C>A (p.Val533=) | |
| 9 | g.91724887A>C | CA373797976 | ROR2 | c.1607T>G (p.Val536Gly) c.1187T>G (p.Val396Gly) n.2075T>G c.404T>G (p.Val135Gly) c.1598T>G (p.Val533Gly) | |
| 9 | g.91724887A>G | CA373797978 | ROR2 | c.1607T>C (p.Val536Ala) c.1187T>C (p.Val396Ala) n.2075T>C c.404T>C (p.Val135Ala) c.1598T>C (p.Val533Ala) | |
| 9 | g.91724887A>T | CA373797979 | ROR2 | c.1607T>A (p.Val536Asp) c.1187T>A (p.Val396Asp) n.2075T>A c.404T>A (p.Val135Asp) c.1598T>A (p.Val533Asp) | |
| 9 | g.91724888C>A | CA373797980 | ROR2 | c.1606G>T (p.Val536Phe) c.1186G>T (p.Val396Phe) n.2074G>T c.403G>T (p.Val135Phe) c.1597G>T (p.Val533Phe) | |
| 9 | g.91724888C= | CA1863923388 | ROR2 | c.1606G= (p.Val536=) c.1186G= (p.Val396=) n.2074G= c.403G= (p.Val135=) c.1597G= (p.Val533=) | |
| 9 | g.91724888C>G | CA373797981 | ROR2 | c.1606G>C (p.Val536Leu) c.1186G>C (p.Val396Leu) n.2074G>C c.403G>C (p.Val135Leu) c.1597G>C (p.Val533Leu) | |
| 9 | g.91724888C>T | CA5120632 | ROR2 | c.1606G>A (p.Val536Ile) c.1186G>A (p.Val396Ile) n.2074G>A c.403G>A (p.Val135Ile) c.1597G>A (p.Val533Ile) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 9 | g.91724888_91724891delinsCGTT | CA1863923389 | ROR2 | c.1603_1606delinsAACG (p.Asn535=) c.1183_1186delinsAACG (p.Asn395=) n.2071_2074delinsAACG c.400_403delinsAACG (p.Asn134=) c.1594_1597delinsAACG (p.Asn532=) | |
| 9 | g.91724889G>A | CA5120634 | ROR2 | c.1605C>T (p.Asn535=) c.1185C>T (p.Asn395=) n.2073C>T c.402C>T (p.Asn134=) c.1596C>T (p.Asn532=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 9 | g.91724889G>C | CA373797985 | ROR2 | c.1605C>G (p.Asn535Lys) c.1185C>G (p.Asn395Lys) n.2073C>G c.402C>G (p.Asn134Lys) c.1596C>G (p.Asn532Lys) | |
| 9 | g.91724889G= | CA1863923392 | ROR2 | c.1605C= (p.Asn535=) c.1185C= (p.Asn395=) n.2073C= c.402C= (p.Asn134=) c.1596C= (p.Asn532=) | |
| 9 | g.91724889G>T | CA373797986 | ROR2 | c.1605C>A (p.Asn535Lys) c.1185C>A (p.Asn395Lys) n.2073C>A c.402C>A (p.Asn134Lys) c.1596C>A (p.Asn532Lys) | |
| 9 | g.91724890_91724892del | CA5120633 | ROR2 | c.1603_1605del (p.Asn535del) c.1183_1185del (p.Asn395del) n.2071_2073del c.400_402del (p.Asn134del) c.1594_1596del (p.Asn532del) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 9 | g.91724890T>A | CA373797990 | ROR2 | c.1604A>T (p.Asn535Ile) c.1184A>T (p.Asn395Ile) n.2072A>T c.401A>T (p.Asn134Ile) c.1595A>T (p.Asn532Ile) | |
| 9 | g.91724890T>C | CA5120635 | ROR2 | c.1604A>G (p.Asn535Ser) c.1184A>G (p.Asn395Ser) n.2072A>G c.401A>G (p.Asn134Ser) c.1595A>G (p.Asn532Ser) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 9 | g.91724890T>G | CA373797991 | ROR2 | c.1604A>C (p.Asn535Thr) c.1184A>C (p.Asn395Thr) n.2072A>C c.401A>C (p.Asn134Thr) c.1595A>C (p.Asn532Thr) | dbSNP |
| 9 | g.91724890T= | CA1863923394 | ROR2 | c.1604A= (p.Asn535=) c.1184A= (p.Asn395=) n.2072A= c.401A= (p.Asn134=) c.1595A= (p.Asn532=) | |
| 9 | g.91724891T>A | CA373797992 | ROR2 | c.1603A>T (p.Asn535Tyr) c.1183A>T (p.Asn395Tyr) n.2071A>T c.400A>T (p.Asn134Tyr) c.1594A>T (p.Asn532Tyr) | |
| 9 | g.91724891T>C | CA373797994 | ROR2 | c.1603A>G (p.Asn535Asp) c.1183A>G (p.Asn395Asp) n.2071A>G c.400A>G (p.Asn134Asp) c.1594A>G (p.Asn532Asp) | gnomAD v4 |
| 9 | g.91724891T>G | CA373797993 | ROR2 | c.1603A>C (p.Asn535His) c.1183A>C (p.Asn395His) n.2071A>C c.400A>C (p.Asn134His) c.1594A>C (p.Asn532His) | |
| 9 | g.91724892G>A | CA466339320 | ROR2 | c.1602C>T (p.Pro534=) c.1182C>T (p.Pro394=) n.2070C>T c.399C>T (p.Pro133=) c.1593C>T (p.Pro531=) | |
| 9 | g.91724892G>C | CA466339321 | ROR2 | c.1602C>G (p.Pro534=) c.1182C>G (p.Pro394=) n.2070C>G c.399C>G (p.Pro133=) c.1593C>G (p.Pro531=) | |
| 9 | g.91724892G= | CA1863923396 | ROR2 | c.1602C= (p.Pro534=) c.1182C= (p.Pro394=) n.2070C= c.399C= (p.Pro133=) c.1593C= (p.Pro531=) | |
| 9 | g.91724892G>T | CA466339322 | ROR2 | c.1602C>A (p.Pro534=) c.1182C>A (p.Pro394=) n.2070C>A c.399C>A (p.Pro133=) c.1593C>A (p.Pro531=) | dbSNP |
| 9 | g.91724893G>A | CA373797996 | ROR2 | c.1601C>T (p.Pro534Leu) c.1181C>T (p.Pro394Leu) n.2069C>T c.398C>T (p.Pro133Leu) c.1592C>T (p.Pro531Leu) | dbSNP gnomAD v4 |
| 9 | g.91724893G>C | CA373797998 | ROR2 | c.1601C>G (p.Pro534Arg) c.1181C>G (p.Pro394Arg) n.2069C>G c.398C>G (p.Pro133Arg) c.1592C>G (p.Pro531Arg) | |
| 9 | g.91724893G= | CA1863923401 | ROR2 | c.1601C= (p.Pro534=) c.1181C= (p.Pro394=) n.2069C= c.398C= (p.Pro133=) c.1592C= (p.Pro531=) | |
| 9 | g.91724893G>T | CA5120636 | ROR2 | c.1601C>A (p.Pro534His) c.1181C>A (p.Pro394His) n.2069C>A c.398C>A (p.Pro133His) c.1592C>A (p.Pro531His) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 9 | g.91724894G>A | CA373798000 | ROR2 | c.1600C>T (p.Pro534Ser) c.1180C>T (p.Pro394Ser) n.2068C>T c.397C>T (p.Pro133Ser) c.1591C>T (p.Pro531Ser) | |
| 9 | g.91724894G>C | CA373798004 | ROR2 | c.1600C>G (p.Pro534Ala) c.1180C>G (p.Pro394Ala) n.2068C>G c.397C>G (p.Pro133Ala) c.1591C>G (p.Pro531Ala) | |
| 9 | g.91724894G>T | CA373798002 | ROR2 | c.1600C>A (p.Pro534Thr) c.1180C>A (p.Pro394Thr) n.2068C>A c.397C>A (p.Pro133Thr) c.1591C>A (p.Pro531Thr) | |
| 9 | g.91724895G>A | CA5120637 | ROR2 | c.1599C>T (p.His533=) c.1179C>T (p.His393=) n.2067C>T c.396C>T (p.His132=) c.1590C>T (p.His530=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 9 | g.91724895G>C | CA373798006 | ROR2 | c.1599C>G (p.His533Gln) c.1179C>G (p.His393Gln) n.2067C>G c.396C>G (p.His132Gln) c.1590C>G (p.His530Gln) | |
| 9 | g.91724895G= | CA1863923403 | ROR2 | c.1599C= (p.His533=) c.1179C= (p.His393=) n.2067C= c.396C= (p.His132=) c.1590C= (p.His530=) | |
| 9 | g.91724895G>T | CA373798007 | ROR2 | c.1599C>A (p.His533Gln) c.1179C>A (p.His393Gln) n.2067C>A c.396C>A (p.His132Gln) c.1590C>A (p.His530Gln) | gnomAD v4 COSMIC |
| 9 | g.91724896T>A | CA373798009 | ROR2 | c.1598A>T (p.His533Leu) c.1178A>T (p.His393Leu) n.2066A>T c.395A>T (p.His132Leu) c.1589A>T (p.His530Leu) | |
| 9 | g.91724896T>C | CA373798011 | ROR2 | c.1598A>G (p.His533Arg) c.1178A>G (p.His393Arg) n.2066A>G c.395A>G (p.His132Arg) c.1589A>G (p.His530Arg) | |
| 9 | g.91724896T>G | CA373798013 | ROR2 | c.1598A>C (p.His533Pro) c.1178A>C (p.His393Pro) n.2066A>C c.395A>C (p.His132Pro) c.1589A>C (p.His530Pro) | dbSNP |
| 9 | g.91724896T= | CA1863923407 | ROR2 | c.1598A= (p.His533=) c.1178A= (p.His393=) n.2066A= c.395A= (p.His132=) c.1589A= (p.His530=) | |
| 9 | g.91724897G>A | CA373798014 | ROR2 | c.1597C>T (p.His533Tyr) c.1177C>T (p.His393Tyr) n.2065C>T c.394C>T (p.His132Tyr) c.1588C>T (p.His530Tyr) | gnomAD v4 |
| 9 | g.91724897G>C | CA373798015 | ROR2 | c.1597C>G (p.His533Asp) c.1177C>G (p.His393Asp) n.2065C>G c.394C>G (p.His132Asp) c.1588C>G (p.His530Asp) | dbSNP gnomAD v2 gnomAD v4 |
| 9 | g.91724897G= | CA1863923409 | ROR2 | c.1597C= (p.His533=) c.1177C= (p.His393=) n.2065C= c.394C= (p.His132=) c.1588C= (p.His530=) | |
| 9 | g.91724897G>T | CA373798017 | ROR2 | c.1597C>A (p.His533Asn) c.1177C>A (p.His393Asn) n.2065C>A c.394C>A (p.His132Asn) c.1588C>A (p.His530Asn) | |
| 9 | g.91724898T>A | CA373798019 | ROR2 | c.1596A>T (p.Gln532His) c.1176A>T (p.Gln392His) n.2064A>T c.393A>T (p.Gln131His) c.1587A>T (p.Gln529His) | |
| 9 | g.91724898T>C | CA5120638 | ROR2 | c.1596A>G (p.Gln532=) c.1176A>G (p.Gln392=) n.2064A>G c.393A>G (p.Gln131=) c.1587A>G (p.Gln529=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 9 | g.91724898T>G | CA373798021 | ROR2 | c.1596A>C (p.Gln532His) c.1176A>C (p.Gln392His) n.2064A>C c.393A>C (p.Gln131His) c.1587A>C (p.Gln529His) | |
| 9 | g.91724898T= | CA1863923411 | ROR2 | c.1596A= (p.Gln532=) c.1176A= (p.Gln392=) n.2064A= c.393A= (p.Gln131=) c.1587A= (p.Gln529=) | |
| 9 | g.91724899T>A | CA373798026 | ROR2 | c.1595A>T (p.Gln532Leu) c.1175A>T (p.Gln392Leu) n.2063A>T c.392A>T (p.Gln131Leu) c.1586A>T (p.Gln529Leu) | |
| 9 | g.91724899T>C | CA5120639 | ROR2 | c.1595A>G (p.Gln532Arg) c.1175A>G (p.Gln392Arg) n.2063A>G c.392A>G (p.Gln131Arg) c.1586A>G (p.Gln529Arg) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 9 | g.91724899T>G | CA373798025 | ROR2 | c.1595A>C (p.Gln532Pro) c.1175A>C (p.Gln392Pro) n.2063A>C c.392A>C (p.Gln131Pro) c.1586A>C (p.Gln529Pro) | dbSNP |
| 9 | g.91724899T= | CA1863923414 | ROR2 | c.1595A= (p.Gln532=) c.1175A= (p.Gln392=) n.2063A= c.392A= (p.Gln131=) c.1586A= (p.Gln529=) | |
| 9 | g.91724900G>A | CA373798028 | ROR2 | c.1594C>T (p.Gln532Ter) c.1174C>T (p.Gln392Ter) n.2062C>T c.391C>T (p.Gln131Ter) c.1585C>T (p.Gln529Ter) | gnomAD v4 |
| 9 | g.91724900G>C | CA373798030 | ROR2 | c.1594C>G (p.Gln532Glu) c.1174C>G (p.Gln392Glu) n.2062C>G c.391C>G (p.Gln131Glu) c.1585C>G (p.Gln529Glu) | |
| 9 | g.91724900G>T | CA373798031 | ROR2 | c.1594C>A (p.Gln532Lys) c.1174C>A (p.Gln392Lys) n.2062C>A c.391C>A (p.Gln131Lys) c.1585C>A (p.Gln529Lys) | |
| 9 | g.91724901C>A | CA466339329 | ROR2 | c.1593G>T (p.Leu531=) c.1173G>T (p.Leu391=) n.2061G>T c.390G>T (p.Leu130=) c.1584G>T (p.Leu528=) | dbSNP gnomAD v2 gnomAD v4 |
| 9 | g.91724901C= | CA1863923416 | ROR2 | c.1593G= (p.Leu531=) c.1173G= (p.Leu391=) n.2061G= c.390G= (p.Leu130=) c.1584G= (p.Leu528=) | |
| 9 | g.91724901C>G | CA466339330 | ROR2 | c.1593G>C (p.Leu531=) c.1173G>C (p.Leu391=) n.2061G>C c.390G>C (p.Leu130=) c.1584G>C (p.Leu528=) | |
| 9 | g.91724901C>T | CA466339331 | ROR2 | c.1593G>A (p.Leu531=) c.1173G>A (p.Leu391=) n.2061G>A c.390G>A (p.Leu130=) c.1584G>A (p.Leu528=) | dbSNP gnomAD v3 gnomAD v4 |
| 9 | g.91724902A>C | CA373798033 | ROR2 | c.1592T>G (p.Leu531Arg) c.1172T>G (p.Leu391Arg) n.2060T>G c.389T>G (p.Leu130Arg) c.1583T>G (p.Leu528Arg) | |
| 9 | g.91724902A>G | CA373798035 | ROR2 | c.1592T>C (p.Leu531Pro) c.1172T>C (p.Leu391Pro) n.2060T>C c.389T>C (p.Leu130Pro) c.1583T>C (p.Leu528Pro) | |
| 9 | g.91724902A>T | CA373798036 | ROR2 | c.1592T>A (p.Leu531Gln) c.1172T>A (p.Leu391Gln) n.2060T>A c.389T>A (p.Leu130Gln) c.1583T>A (p.Leu528Gln) | |
| 9 | g.91724903G>A | CA466339334 | ROR2 | c.1591C>T (p.Leu531=) c.1171C>T (p.Leu391=) n.2059C>T c.388C>T (p.Leu130=) c.1582C>T (p.Leu528=) | |
| 9 | g.91724903G>C | CA373798038 | ROR2 | c.1591C>G (p.Leu531Val) c.1171C>G (p.Leu391Val) n.2059C>G c.388C>G (p.Leu130Val) c.1582C>G (p.Leu528Val) | |
| 9 | g.91724903G>T | CA373798039 | ROR2 | c.1591C>A (p.Leu531Met) c.1171C>A (p.Leu391Met) n.2059C>A c.388C>A (p.Leu130Met) c.1582C>A (p.Leu528Met) | |
| 9 | g.91724904C>A | CA466339335 | ROR2 | c.1590G>T (p.Arg530=) c.1170G>T (p.Arg390=) n.2058G>T c.387G>T (p.Arg129=) c.1581G>T (p.Arg527=) | gnomAD v4 |
| 9 | g.91724904C= | CA1863923418 | ROR2 | c.1590G= (p.Arg530=) c.1170G= (p.Arg390=) n.2058G= c.387G= (p.Arg129=) c.1581G= (p.Arg527=) | |
| 9 | g.91724904C>G | CA466339336 | ROR2 | c.1590G>C (p.Arg530=) c.1170G>C (p.Arg390=) n.2058G>C c.387G>C (p.Arg129=) c.1581G>C (p.Arg527=) | dbSNP |
| 9 | g.91724904C>T | CA466339337 | ROR2 | c.1590G>A (p.Arg530=) c.1170G>A (p.Arg390=) n.2058G>A c.387G>A (p.Arg129=) c.1581G>A (p.Arg527=) | |
| 9 | g.91724905C>A | CA373798041 | ROR2 | c.1589G>T (p.Arg530Leu) c.1169G>T (p.Arg390Leu) n.2057G>T c.386G>T (p.Arg129Leu) c.1580G>T (p.Arg527Leu) | |
| 9 | g.91724905C= | CA1863923420 | ROR2 | c.1589G= (p.Arg530=) c.1169G= (p.Arg390=) n.2057G= c.386G= (p.Arg129=) c.1580G= (p.Arg527=) | |
| 9 | g.91724905C>G | CA373798043 | ROR2 | c.1589G>C (p.Arg530Pro) c.1169G>C (p.Arg390Pro) n.2057G>C c.386G>C (p.Arg129Pro) c.1580G>C (p.Arg527Pro) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 9 | g.91724905C>T | CA5120640 | ROR2 | c.1589G>A (p.Arg530Gln) c.1169G>A (p.Arg390Gln) n.2057G>A c.386G>A (p.Arg129Gln) c.1580G>A (p.Arg527Gln) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |