Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
9 | g.91724425A>C | CA373796271 | ROR2 | c.2069T>G (p.Leu690Arg) c.1649T>G (p.Leu550Arg) n.2537T>G c.866T>G (p.Leu289Arg) c.2060T>G (p.Leu687Arg) | |
9 | g.91724425A>G | CA373796267 | ROR2 | c.2069T>C (p.Leu690Pro) c.1649T>C (p.Leu550Pro) n.2537T>C c.866T>C (p.Leu289Pro) c.2060T>C (p.Leu687Pro) | gnomAD v4 |
9 | g.91724425A>T | CA373796269 | ROR2 | c.2069T>A (p.Leu690Gln) c.1649T>A (p.Leu550Gln) n.2537T>A c.866T>A (p.Leu289Gln) c.2060T>A (p.Leu687Gln) | gnomAD v4 |
9 | g.91724426G>A | CA466339027 | ROR2 | c.2068C>T (p.Leu690=) c.1648C>T (p.Leu550=) n.2536C>T c.865C>T (p.Leu289=) c.2059C>T (p.Leu687=) | gnomAD v4 |
9 | g.91724426G>C | CA373796273 | ROR2 | c.2068C>G (p.Leu690Val) c.1648C>G (p.Leu550Val) n.2536C>G c.865C>G (p.Leu289Val) c.2059C>G (p.Leu687Val) | |
9 | g.91724426G>T | CA373796275 | ROR2 | c.2068C>A (p.Leu690Met) c.1648C>A (p.Leu550Met) n.2536C>A c.865C>A (p.Leu289Met) c.2059C>A (p.Leu687Met) | COSMIC |
9 | g.91724427G>A | CA466339030 | ROR2 | c.2067C>T (p.Gly689=) c.1647C>T (p.Gly549=) n.2535C>T c.864C>T (p.Gly288=) c.2058C>T (p.Gly686=) | ClinVar |
9 | g.91724427G>C | CA466339029 | ROR2 | c.2067C>G (p.Gly689=) c.1647C>G (p.Gly549=) n.2535C>G c.864C>G (p.Gly288=) c.2058C>G (p.Gly686=) | |
9 | g.91724427G>T | CA466339028 | ROR2 | c.2067C>A (p.Gly689=) c.1647C>A (p.Gly549=) n.2535C>A c.864C>A (p.Gly288=) c.2058C>A (p.Gly686=) | |
9 | g.91724428C>A | CA373796276 | ROR2 | c.2066G>T (p.Gly689Val) c.1646G>T (p.Gly549Val) n.2534G>T c.863G>T (p.Gly288Val) c.2057G>T (p.Gly686Val) | |
9 | g.91724428C>G | CA373796278 | ROR2 | c.2066G>C (p.Gly689Ala) c.1646G>C (p.Gly549Ala) n.2534G>C c.863G>C (p.Gly288Ala) c.2057G>C (p.Gly686Ala) | |
9 | g.91724428C>T | CA373796283 | ROR2 | c.2066G>A (p.Gly689Asp) c.1646G>A (p.Gly549Asp) n.2534G>A c.863G>A (p.Gly288Asp) c.2057G>A (p.Gly686Asp) | gnomAD v4 |
9 | g.91724429C>A | CA373796285 | ROR2 | c.2065G>T (p.Gly689Cys) c.1645G>T (p.Gly549Cys) n.2533G>T c.862G>T (p.Gly288Cys) c.2056G>T (p.Gly686Cys) | |
9 | g.91724429C= | CA1863922762 | ROR2 | c.2065G= (p.Gly689=) c.1645G= (p.Gly549=) n.2533G= c.862G= (p.Gly288=) c.2056G= (p.Gly686=) | |
9 | g.91724429C>G | CA373796288 | ROR2 | c.2065G>C (p.Gly689Arg) c.1645G>C (p.Gly549Arg) n.2533G>C c.862G>C (p.Gly288Arg) c.2056G>C (p.Gly686Arg) | |
9 | g.91724429C>T | CA5120497 | ROR2 | c.2065G>A (p.Gly689Ser) c.1645G>A (p.Gly549Ser) n.2533G>A c.862G>A (p.Gly288Ser) c.2056G>A (p.Gly686Ser) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC |
9 | g.91724430G>A | CA5120498 | ROR2 | c.2064C>T (p.Tyr688=) c.1644C>T (p.Tyr548=) n.2532C>T c.861C>T (p.Tyr287=) c.2055C>T (p.Tyr685=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
9 | g.91724430G>C | CA373796289 | ROR2 | c.2064C>G (p.Tyr688Ter) c.1644C>G (p.Tyr548Ter) n.2532C>G c.861C>G (p.Tyr287Ter) c.2055C>G (p.Tyr685Ter) | |
9 | g.91724430G= | CA1863922769 | ROR2 | c.2064C= (p.Tyr688=) c.1644C= (p.Tyr548=) n.2532C= c.861C= (p.Tyr287=) c.2055C= (p.Tyr685=) | |
9 | g.91724430G>T | CA373796290 | ROR2 | c.2064C>A (p.Tyr688Ter) c.1644C>A (p.Tyr548Ter) n.2532C>A c.861C>A (p.Tyr287Ter) c.2055C>A (p.Tyr685Ter) | dbSNP |
9 | g.91724431T>A | CA373796291 | ROR2 | c.2063A>T (p.Tyr688Phe) c.1643A>T (p.Tyr548Phe) n.2531A>T c.860A>T (p.Tyr287Phe) c.2054A>T (p.Tyr685Phe) | |
9 | g.91724431T>C | CA373796292 | ROR2 | c.2063A>G (p.Tyr688Cys) c.1643A>G (p.Tyr548Cys) n.2531A>G c.860A>G (p.Tyr287Cys) c.2054A>G (p.Tyr685Cys) | |
9 | g.91724431T>G | CA373796293 | ROR2 | c.2063A>C (p.Tyr688Ser) c.1643A>C (p.Tyr548Ser) n.2531A>C c.860A>C (p.Tyr287Ser) c.2054A>C (p.Tyr685Ser) | |
9 | g.91724432A= | CA1863922774 | ROR2 | c.2062T= (p.Tyr688=) c.1642T= (p.Tyr548=) n.2530T= c.859T= (p.Tyr287=) c.2053T= (p.Tyr685=) | |
9 | g.91724432A>C | CA5120499 | ROR2 | c.2062T>G (p.Tyr688Asp) c.1642T>G (p.Tyr548Asp) n.2530T>G c.859T>G (p.Tyr287Asp) c.2053T>G (p.Tyr685Asp) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.91724432A>G | CA373796298 | ROR2 | c.2062T>C (p.Tyr688His) c.1642T>C (p.Tyr548His) n.2530T>C c.859T>C (p.Tyr287His) c.2053T>C (p.Tyr685His) | |
9 | g.91724432A>T | CA195322938 | ROR2 | c.2062T>A (p.Tyr688Asn) c.1642T>A (p.Tyr548Asn) n.2530T>A c.859T>A (p.Tyr287Asn) c.2053T>A (p.Tyr685Asn) | dbSNP gnomAD v4 |
9 | g.91724433G>A | CA466339031 | ROR2 | c.2061C>T (p.Ser687=) c.1641C>T (p.Ser547=) n.2529C>T c.858C>T (p.Ser286=) c.2052C>T (p.Ser684=) | |
9 | g.91724433G>C | CA373796303 | ROR2 | c.2061C>G (p.Ser687Arg) c.1641C>G (p.Ser547Arg) n.2529C>G c.858C>G (p.Ser286Arg) c.2052C>G (p.Ser684Arg) | |
9 | g.91724433G>T | CA373796305 | ROR2 | c.2061C>A (p.Ser687Arg) c.1641C>A (p.Ser547Arg) n.2529C>A c.858C>A (p.Ser286Arg) c.2052C>A (p.Ser684Arg) | |
9 | g.91724434C>A | CA373796307 | ROR2 | c.2060G>T (p.Ser687Ile) c.1640G>T (p.Ser547Ile) n.2528G>T c.857G>T (p.Ser286Ile) c.2051G>T (p.Ser684Ile) | gnomAD v4 |
9 | g.91724434C>G | CA373796310 | ROR2 | c.2060G>C (p.Ser687Thr) c.1640G>C (p.Ser547Thr) n.2528G>C c.857G>C (p.Ser286Thr) c.2051G>C (p.Ser684Thr) | |
9 | g.91724434C>T | CA373796311 | ROR2 | c.2060G>A (p.Ser687Asn) c.1640G>A (p.Ser547Asn) n.2528G>A c.857G>A (p.Ser286Asn) c.2051G>A (p.Ser684Asn) | gnomAD v4 |
9 | g.91724435T>A | CA373796313 | ROR2 | c.2059A>T (p.Ser687Cys) c.1639A>T (p.Ser547Cys) n.2527A>T c.856A>T (p.Ser286Cys) c.2050A>T (p.Ser684Cys) | |
9 | g.91724435T>C | CA373796318 | ROR2 | c.2059A>G (p.Ser687Gly) c.1639A>G (p.Ser547Gly) n.2527A>G c.856A>G (p.Ser286Gly) c.2050A>G (p.Ser684Gly) | gnomAD v4 |
9 | g.91724435T>G | CA373796315 | ROR2 | c.2059A>C (p.Ser687Arg) c.1639A>C (p.Ser547Arg) n.2527A>C c.856A>C (p.Ser286Arg) c.2050A>C (p.Ser684Arg) | |
9 | g.91724436G>A | CA466339032 | ROR2 | c.2058C>T (p.Phe686=) c.1638C>T (p.Phe546=) n.2526C>T c.855C>T (p.Phe285=) c.2049C>T (p.Phe683=) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.91724436G>C | CA5120500 | ROR2 | c.2058C>G (p.Phe686Leu) c.1638C>G (p.Phe546Leu) n.2526C>G c.855C>G (p.Phe285Leu) c.2049C>G (p.Phe683Leu) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.91724436G= | CA1863922776 | ROR2 | c.2058C= (p.Phe686=) c.1638C= (p.Phe546=) n.2526C= c.855C= (p.Phe285=) c.2049C= (p.Phe683=) | |
9 | g.91724436G>T | CA5120501 | ROR2 | c.2058C>A (p.Phe686Leu) c.1638C>A (p.Phe546Leu) n.2526C>A c.855C>A (p.Phe285Leu) c.2049C>A (p.Phe683Leu) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.91724437A>C | CA373796322 | ROR2 | c.2057T>G (p.Phe686Cys) c.1637T>G (p.Phe546Cys) n.2525T>G c.854T>G (p.Phe285Cys) c.2048T>G (p.Phe683Cys) | |
9 | g.91724437A>G | CA373796324 | ROR2 | c.2057T>C (p.Phe686Ser) c.1637T>C (p.Phe546Ser) n.2525T>C c.854T>C (p.Phe285Ser) c.2048T>C (p.Phe683Ser) | |
9 | g.91724437A>T | CA373796326 | ROR2 | c.2057T>A (p.Phe686Tyr) c.1637T>A (p.Phe546Tyr) n.2525T>A c.854T>A (p.Phe285Tyr) c.2048T>A (p.Phe683Tyr) | |
9 | g.91724438A= | CA1863922779 | ROR2 | c.2056T= (p.Phe686=) c.1636T= (p.Phe546=) n.2524T= c.853T= (p.Phe285=) c.2047T= (p.Phe683=) | |
9 | g.91724438A>C | CA373796328 | ROR2 | c.2056T>G (p.Phe686Val) c.1636T>G (p.Phe546Val) n.2524T>G c.853T>G (p.Phe285Val) c.2047T>G (p.Phe683Val) | |
9 | g.91724438A>G | CA373796330 | ROR2 | c.2056T>C (p.Phe686Leu) c.1636T>C (p.Phe546Leu) n.2524T>C c.853T>C (p.Phe285Leu) c.2047T>C (p.Phe683Leu) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.91724438A>T | CA373796334 | ROR2 | c.2056T>A (p.Phe686Ile) c.1636T>A (p.Phe546Ile) n.2524T>A c.853T>A (p.Phe285Ile) c.2047T>A (p.Phe683Ile) | |
9 | g.91724439G>A | CA466339033 | ROR2 | c.2055C>T (p.Val685=) c.1635C>T (p.Val545=) n.2523C>T c.852C>T (p.Val284=) c.2046C>T (p.Val682=) | dbSNP gnomAD v4 |
9 | g.91724439G>C | CA466339036 | ROR2 | c.2055C>G (p.Val685=) c.1635C>G (p.Val545=) n.2523C>G c.852C>G (p.Val284=) c.2046C>G (p.Val682=) | |
9 | g.91724439G= | CA1863922781 | ROR2 | c.2055C= (p.Val685=) c.1635C= (p.Val545=) n.2523C= c.852C= (p.Val284=) c.2046C= (p.Val682=) | |
9 | g.91724439G>T | CA466339035 | ROR2 | c.2055C>A (p.Val685=) c.1635C>A (p.Val545=) n.2523C>A c.852C>A (p.Val284=) c.2046C>A (p.Val682=) | |
9 | g.91724440A>C | CA373796336 | ROR2 | c.2054T>G (p.Val685Gly) c.1634T>G (p.Val545Gly) n.2522T>G c.851T>G (p.Val284Gly) c.2045T>G (p.Val682Gly) | |
9 | g.91724440A>G | CA373796337 | ROR2 | c.2054T>C (p.Val685Ala) c.1634T>C (p.Val545Ala) n.2522T>C c.851T>C (p.Val284Ala) c.2045T>C (p.Val682Ala) | |
9 | g.91724440A>T | CA373796338 | ROR2 | c.2054T>A (p.Val685Asp) c.1634T>A (p.Val545Asp) n.2522T>A c.851T>A (p.Val284Asp) c.2045T>A (p.Val682Asp) | |
9 | g.91724441C>A | CA373796340 | ROR2 | c.2053G>T (p.Val685Phe) c.1633G>T (p.Val545Phe) n.2521G>T c.850G>T (p.Val284Phe) c.2044G>T (p.Val682Phe) | |
9 | g.91724441C= | CA1863922785 | ROR2 | c.2053G= (p.Val685=) c.1633G= (p.Val545=) n.2521G= c.850G= (p.Val284=) c.2044G= (p.Val682=) | |
9 | g.91724441C>G | CA373796347 | ROR2 | c.2053G>C (p.Val685Leu) c.1633G>C (p.Val545Leu) n.2521G>C c.850G>C (p.Val284Leu) c.2044G>C (p.Val682Leu) | |
9 | g.91724441C>T | CA373796343 | ROR2 | c.2053G>A (p.Val685Ile) c.1633G>A (p.Val545Ile) n.2521G>A c.850G>A (p.Val284Ile) c.2044G>A (p.Val682Ile) | dbSNP gnomAD v2 gnomAD v4 |
9 | g.91724442C>A | CA373796350 | ROR2 | c.2052G>T (p.Glu684Asp) c.1632G>T (p.Glu544Asp) n.2520G>T c.849G>T (p.Glu283Asp) c.2043G>T (p.Glu681Asp) | |
9 | g.91724442C= | CA1863922786 | ROR2 | c.2052G= (p.Glu684=) c.1632G= (p.Glu544=) n.2520G= c.849G= (p.Glu283=) c.2043G= (p.Glu681=) | |
9 | g.91724442C>G | CA373796354 | ROR2 | c.2052G>C (p.Glu684Asp) c.1632G>C (p.Glu544Asp) n.2520G>C c.849G>C (p.Glu283Asp) c.2043G>C (p.Glu681Asp) | |
9 | g.91724442C>T | CA5120502 | ROR2 | c.2052G>A (p.Glu684=) c.1632G>A (p.Glu544=) n.2520G>A c.849G>A (p.Glu283=) c.2043G>A (p.Glu681=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
9 | g.91724443T>A | CA373796362 | ROR2 | c.2051A>T (p.Glu684Val) c.1631A>T (p.Glu544Val) n.2519A>T c.848A>T (p.Glu283Val) c.2042A>T (p.Glu681Val) | |
9 | g.91724443T>C | CA373796363 | ROR2 | c.2051A>G (p.Glu684Gly) c.1631A>G (p.Glu544Gly) n.2519A>G c.848A>G (p.Glu283Gly) c.2042A>G (p.Glu681Gly) | |
9 | g.91724443T>G | CA373796366 | ROR2 | c.2051A>C (p.Glu684Ala) c.1631A>C (p.Glu544Ala) n.2519A>C c.848A>C (p.Glu283Ala) c.2042A>C (p.Glu681Ala) | dbSNP gnomAD v2 gnomAD v4 |
9 | g.91724443T= | CA1863922787 | ROR2 | c.2051A= (p.Glu684=) c.1631A= (p.Glu544=) n.2519A= c.848A= (p.Glu283=) c.2042A= (p.Glu681=) | |
9 | g.91724444C>A | CA373796370 | ROR2 | c.2050G>T (p.Glu684Ter) c.1630G>T (p.Glu544Ter) n.2518G>T c.847G>T (p.Glu283Ter) c.2041G>T (p.Glu681Ter) | |
9 | g.91724444C>G | CA373796369 | ROR2 | c.2050G>C (p.Glu684Gln) c.1630G>C (p.Glu544Gln) n.2518G>C c.847G>C (p.Glu283Gln) c.2041G>C (p.Glu681Gln) | |
9 | g.91724444C>T | CA373796368 | ROR2 | c.2050G>A (p.Glu684Lys) c.1630G>A (p.Glu544Lys) n.2518G>A c.847G>A (p.Glu283Lys) c.2041G>A (p.Glu681Lys) | |
9 | g.91724445C>A | CA373796371 | ROR2 | c.2049G>T (p.Trp683Cys) c.1629G>T (p.Trp543Cys) n.2517G>T c.846G>T (p.Trp282Cys) c.2040G>T (p.Trp680Cys) | |
9 | g.91724445C= | CA1863922791 | ROR2 | c.2049G= (p.Trp683=) c.1629G= (p.Trp543=) n.2517G= c.846G= (p.Trp282=) c.2040G= (p.Trp680=) | |
9 | g.91724445C>G | CA373796372 | ROR2 | c.2049G>C (p.Trp683Cys) c.1629G>C (p.Trp543Cys) n.2517G>C c.846G>C (p.Trp282Cys) c.2040G>C (p.Trp680Cys) | |
9 | g.91724445C>T | CA195322979 | ROR2 | c.2049G>A (p.Trp683Ter) c.1629G>A (p.Trp543Ter) n.2517G>A c.846G>A (p.Trp282Ter) c.2040G>A (p.Trp680Ter) | dbSNP |
9 | g.91724446C>A | CA373796373 | ROR2 | c.2048G>T (p.Trp683Leu) c.1628G>T (p.Trp543Leu) n.2516G>T c.845G>T (p.Trp282Leu) c.2039G>T (p.Trp680Leu) | |
9 | g.91724446C>G | CA373796374 | ROR2 | c.2048G>C (p.Trp683Ser) c.1628G>C (p.Trp543Ser) n.2516G>C c.845G>C (p.Trp282Ser) c.2039G>C (p.Trp680Ser) | |
9 | g.91724446C>T | CA373796376 | ROR2 | c.2048G>A (p.Trp683Ter) c.1628G>A (p.Trp543Ter) n.2516G>A c.845G>A (p.Trp282Ter) c.2039G>A (p.Trp680Ter) | |
9 | g.91724447A>C | CA373796379 | ROR2 | c.2047T>G (p.Trp683Gly) c.1627T>G (p.Trp543Gly) n.2515T>G c.844T>G (p.Trp282Gly) c.2038T>G (p.Trp680Gly) | |
9 | g.91724447A>G | CA373796382 | ROR2 | c.2047T>C (p.Trp683Arg) c.1627T>C (p.Trp543Arg) n.2515T>C c.844T>C (p.Trp282Arg) c.2038T>C (p.Trp680Arg) | |
9 | g.91724447A>T | CA373796380 | ROR2 | c.2047T>A (p.Trp683Arg) c.1627T>A (p.Trp543Arg) n.2515T>A c.844T>A (p.Trp282Arg) c.2038T>A (p.Trp680Arg) | |
9 | g.91724448C>A | CA466339042 | ROR2 | c.2046G>T (p.Leu682=) c.1626G>T (p.Leu542=) n.2514G>T c.843G>T (p.Leu281=) c.2037G>T (p.Leu679=) | |
9 | g.91724448C>G | CA466339043 | ROR2 | c.2046G>C (p.Leu682=) c.1626G>C (p.Leu542=) n.2514G>C c.843G>C (p.Leu281=) c.2037G>C (p.Leu679=) | |
9 | g.91724448C>T | CA466339044 | ROR2 | c.2046G>A (p.Leu682=) c.1626G>A (p.Leu542=) n.2514G>A c.843G>A (p.Leu281=) c.2037G>A (p.Leu679=) | |
9 | g.91724449A>C | CA373796385 | ROR2 | c.2045T>G (p.Leu682Arg) c.1625T>G (p.Leu542Arg) n.2513T>G c.842T>G (p.Leu281Arg) c.2036T>G (p.Leu679Arg) | |
9 | g.91724449A>G | CA373796387 | ROR2 | c.2045T>C (p.Leu682Pro) c.1625T>C (p.Leu542Pro) n.2513T>C c.842T>C (p.Leu281Pro) c.2036T>C (p.Leu679Pro) | |
9 | g.91724449A>T | CA373796388 | ROR2 | c.2045T>A (p.Leu682Gln) c.1625T>A (p.Leu542Gln) n.2513T>A c.842T>A (p.Leu281Gln) c.2036T>A (p.Leu679Gln) | |
9 | g.91724450G>A | CA466339045 | ROR2 | c.2044C>T (p.Leu682=) c.1624C>T (p.Leu542=) n.2512C>T c.841C>T (p.Leu281=) c.2035C>T (p.Leu679=) | |
9 | g.91724450G>C | CA373796390 | ROR2 | c.2044C>G (p.Leu682Val) c.1624C>G (p.Leu542Val) n.2512C>G c.841C>G (p.Leu281Val) c.2035C>G (p.Leu679Val) | |
9 | g.91724450G>T | CA373796393 | ROR2 | c.2044C>A (p.Leu682Met) c.1624C>A (p.Leu542Met) n.2512C>A c.841C>A (p.Leu281Met) c.2035C>A (p.Leu679Met) | |
9 | g.91724451G>A | CA5120503 | ROR2 | c.2043C>T (p.Val681=) c.1623C>T (p.Val541=) n.2511C>T c.840C>T (p.Val280=) c.2034C>T (p.Val678=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
9 | g.91724451G>C | CA466339049 | ROR2 | c.2043C>G (p.Val681=) c.1623C>G (p.Val541=) n.2511C>G c.840C>G (p.Val280=) c.2034C>G (p.Val678=) | |
9 | g.91724451G= | CA1863922792 | ROR2 | c.2043C= (p.Val681=) c.1623C= (p.Val541=) n.2511C= c.840C= (p.Val280=) c.2034C= (p.Val678=) | |
9 | g.91724451G>T | CA466339050 | ROR2 | c.2043C>A (p.Val681=) c.1623C>A (p.Val541=) n.2511C>A c.840C>A (p.Val280=) c.2034C>A (p.Val678=) | |
9 | g.91724452A>C | CA373796397 | ROR2 | c.2042T>G (p.Val681Gly) c.1622T>G (p.Val541Gly) n.2510T>G c.839T>G (p.Val280Gly) c.2033T>G (p.Val678Gly) | gnomAD v4 |
9 | g.91724452A>G | CA373796399 | ROR2 | c.2042T>C (p.Val681Ala) c.1622T>C (p.Val541Ala) n.2510T>C c.839T>C (p.Val280Ala) c.2033T>C (p.Val678Ala) | |
9 | g.91724452A>T | CA373796401 | ROR2 | c.2042T>A (p.Val681Asp) c.1622T>A (p.Val541Asp) n.2510T>A c.839T>A (p.Val280Asp) c.2033T>A (p.Val678Asp) | |
9 | g.91724453C>A | CA373796402 | ROR2 | c.2041G>T (p.Val681Phe) c.1621G>T (p.Val541Phe) n.2509G>T c.838G>T (p.Val280Phe) c.2032G>T (p.Val678Phe) | COSMIC |
9 | g.91724453C>G | CA373796403 | ROR2 | c.2041G>C (p.Val681Leu) c.1621G>C (p.Val541Leu) n.2509G>C c.838G>C (p.Val280Leu) c.2032G>C (p.Val678Leu) | gnomAD v4 |
9 | g.91724453C>T | CA373796404 | ROR2 | c.2041G>A (p.Val681Ile) c.1621G>A (p.Val541Ile) n.2509G>A c.838G>A (p.Val280Ile) c.2032G>A (p.Val678Ile) | |
9 | g.91724454C>A | CA466339052 | ROR2 | c.2040G>T (p.Val680=) c.1620G>T (p.Val540=) n.2508G>T c.837G>T (p.Val279=) c.2031G>T (p.Val677=) | |
9 | g.91724454C>G | CA466339056 | ROR2 | c.2040G>C (p.Val680=) c.1620G>C (p.Val540=) n.2508G>C c.837G>C (p.Val279=) c.2031G>C (p.Val677=) | |
9 | g.91724454C>T | CA466339054 | ROR2 | c.2040G>A (p.Val680=) c.1620G>A (p.Val540=) n.2508G>A c.837G>A (p.Val279=) c.2031G>A (p.Val677=) | |
9 | g.91724455A= | CA1863922793 | ROR2 | c.2039T= (p.Val680=) c.1619T= (p.Val540=) n.2507T= c.836T= (p.Val279=) c.2030T= (p.Val677=) | |
9 | g.91724455A>C | CA373796405 | ROR2 | c.2039T>G (p.Val680Gly) c.1619T>G (p.Val540Gly) n.2507T>G c.836T>G (p.Val279Gly) c.2030T>G (p.Val677Gly) | |
9 | g.91724455A>G | CA373796409 | ROR2 | c.2039T>C (p.Val680Ala) c.1619T>C (p.Val540Ala) n.2507T>C c.836T>C (p.Val279Ala) c.2030T>C (p.Val677Ala) | dbSNP |
9 | g.91724455A>T | CA373796407 | ROR2 | c.2039T>A (p.Val680Glu) c.1619T>A (p.Val540Glu) n.2507T>A c.836T>A (p.Val279Glu) c.2030T>A (p.Val677Glu) | |
9 | g.91724456C>A | CA373796413 | ROR2 | c.2038G>T (p.Val680Leu) c.1618G>T (p.Val540Leu) n.2506G>T c.835G>T (p.Val279Leu) c.2029G>T (p.Val677Leu) | |
9 | g.91724456C>G | CA373796414 | ROR2 | c.2038G>C (p.Val680Leu) c.1618G>C (p.Val540Leu) n.2506G>C c.835G>C (p.Val279Leu) c.2029G>C (p.Val677Leu) | |
9 | g.91724456C>T | CA373796416 | ROR2 | c.2038G>A (p.Val680Met) c.1618G>A (p.Val540Met) n.2506G>A c.835G>A (p.Val279Met) c.2029G>A (p.Val677Met) | |
9 | g.91724457A>C | CA466339057 | ROR2 | c.2037T>G (p.Gly679=) c.1617T>G (p.Gly539=) n.2505T>G c.834T>G (p.Gly278=) c.2028T>G (p.Gly676=) | |
9 | g.91724457A>G | CA466339058 | ROR2 | c.2037T>C (p.Gly679=) c.1617T>C (p.Gly539=) n.2505T>C c.834T>C (p.Gly278=) c.2028T>C (p.Gly676=) | |
9 | g.91724457A>T | CA466339059 | ROR2 | c.2037T>A (p.Gly679=) c.1617T>A (p.Gly539=) n.2505T>A c.834T>A (p.Gly278=) c.2028T>A (p.Gly676=) | |
9 | g.91724458C>A | CA373796417 | ROR2 | c.2036G>T (p.Gly679Val) c.1616G>T (p.Gly539Val) n.2504G>T c.833G>T (p.Gly278Val) c.2027G>T (p.Gly676Val) | |
9 | g.91724458C>G | CA373796418 | ROR2 | c.2036G>C (p.Gly679Ala) c.1616G>C (p.Gly539Ala) n.2504G>C c.833G>C (p.Gly278Ala) c.2027G>C (p.Gly676Ala) | |
9 | g.91724458C>T | CA373796419 | ROR2 | c.2036G>A (p.Gly679Asp) c.1616G>A (p.Gly539Asp) n.2504G>A c.833G>A (p.Gly278Asp) c.2027G>A (p.Gly676Asp) | COSMIC |
9 | g.91724459C>A | CA373796420 | ROR2 | c.2035G>T (p.Gly679Cys) c.1615G>T (p.Gly539Cys) n.2503G>T c.832G>T (p.Gly278Cys) c.2026G>T (p.Gly676Cys) | |
9 | g.91724459C= | CA1863922795 | ROR2 | c.2035G= (p.Gly679=) c.1615G= (p.Gly539=) n.2503G= c.832G= (p.Gly278=) c.2026G= (p.Gly676=) | |
9 | g.91724459C>G | CA373796422 | ROR2 | c.2035G>C (p.Gly679Arg) c.1615G>C (p.Gly539Arg) n.2503G>C c.832G>C (p.Gly278Arg) c.2026G>C (p.Gly676Arg) | |
9 | g.91724459C>T | CA373796423 | ROR2 | c.2035G>A (p.Gly679Ser) c.1615G>A (p.Gly539Ser) n.2503G>A c.832G>A (p.Gly278Ser) c.2026G>A (p.Gly676Ser) | dbSNP gnomAD v4 COSMIC |
9 | g.91724460G>A | CA5120504 | ROR2 | c.2034C>T (p.Tyr678=) c.1614C>T (p.Tyr538=) n.2502C>T c.831C>T (p.Tyr277=) c.2025C>T (p.Tyr675=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.91724460G>C | CA373796426 | ROR2 | c.2034C>G (p.Tyr678Ter) c.1614C>G (p.Tyr538Ter) n.2502C>G c.831C>G (p.Tyr277Ter) c.2025C>G (p.Tyr675Ter) | |
9 | g.91724460G= | CA1863922798 | ROR2 | c.2034C= (p.Tyr678=) c.1614C= (p.Tyr538=) n.2502C= c.831C= (p.Tyr277=) c.2025C= (p.Tyr675=) | |
9 | g.91724460G>T | CA373796427 | ROR2 | c.2034C>A (p.Tyr678Ter) c.1614C>A (p.Tyr538Ter) n.2502C>A c.831C>A (p.Tyr277Ter) c.2025C>A (p.Tyr675Ter) | dbSNP gnomAD v2 gnomAD v4 |
9 | g.91724461T>A | CA373796434 | ROR2 | c.2033A>T (p.Tyr678Phe) c.1613A>T (p.Tyr538Phe) n.2501A>T c.830A>T (p.Tyr277Phe) c.2024A>T (p.Tyr675Phe) | |
9 | g.91724461T>C | CA373796430 | ROR2 | c.2033A>G (p.Tyr678Cys) c.1613A>G (p.Tyr538Cys) n.2501A>G c.830A>G (p.Tyr277Cys) c.2024A>G (p.Tyr675Cys) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
9 | g.91724461T>G | CA373796429 | ROR2 | c.2033A>C (p.Tyr678Ser) c.1613A>C (p.Tyr538Ser) n.2501A>C c.830A>C (p.Tyr277Ser) c.2024A>C (p.Tyr675Ser) | |
9 | g.91724461T= | CA1863922800 | ROR2 | c.2033A= (p.Tyr678=) c.1613A= (p.Tyr538=) n.2501A= c.830A= (p.Tyr277=) c.2024A= (p.Tyr675=) | |
9 | g.91724462A>C | CA373796435 | ROR2 | c.2032T>G (p.Tyr678Asp) c.1612T>G (p.Tyr538Asp) n.2500T>G c.829T>G (p.Tyr277Asp) c.2023T>G (p.Tyr675Asp) | |
9 | g.91724462A>G | CA373796437 | ROR2 | c.2032T>C (p.Tyr678His) c.1612T>C (p.Tyr538His) n.2500T>C c.829T>C (p.Tyr277His) c.2023T>C (p.Tyr675His) | |
9 | g.91724462A>T | CA373796440 | ROR2 | c.2032T>A (p.Tyr678Asn) c.1612T>A (p.Tyr538Asn) n.2500T>A c.829T>A (p.Tyr277Asn) c.2023T>A (p.Tyr675Asn) | |
9 | g.91724463G>A | CA466339063 | ROR2 | c.2031C>T (p.Ser677=) c.1611C>T (p.Ser537=) n.2499C>T c.828C>T (p.Ser276=) c.2022C>T (p.Ser674=) | |
9 | g.91724463G>C | CA466339064 | ROR2 | c.2031C>G (p.Ser677=) c.1611C>G (p.Ser537=) n.2499C>G c.828C>G (p.Ser276=) c.2022C>G (p.Ser674=) | dbSNP gnomAD v2 gnomAD v4 |
9 | g.91724463G= | CA1863922802 | ROR2 | c.2031C= (p.Ser677=) c.1611C= (p.Ser537=) n.2499C= c.828C= (p.Ser276=) c.2022C= (p.Ser674=) | |
9 | g.91724463G>T | CA466339065 | ROR2 | c.2031C>A (p.Ser677=) c.1611C>A (p.Ser537=) n.2499C>A c.828C>A (p.Ser276=) c.2022C>A (p.Ser674=) | |
9 | g.91724464G>A | CA373796443 | ROR2 | c.2030C>T (p.Ser677Phe) c.1610C>T (p.Ser537Phe) n.2498C>T c.827C>T (p.Ser276Phe) c.2021C>T (p.Ser674Phe) | ClinVar dbSNP |
9 | g.91724464G>C | CA373796446 | ROR2 | c.2030C>G (p.Ser677Cys) c.1610C>G (p.Ser537Cys) n.2498C>G c.827C>G (p.Ser276Cys) c.2021C>G (p.Ser674Cys) | |
9 | g.91724464G>T | CA373796448 | ROR2 | c.2030C>A (p.Ser677Tyr) c.1610C>A (p.Ser537Tyr) n.2498C>A c.827C>A (p.Ser276Tyr) c.2021C>A (p.Ser674Tyr) | |
9 | g.91724465A>C | CA373796449 | ROR2 | c.2029T>G (p.Ser677Ala) c.1609T>G (p.Ser537Ala) n.2497T>G c.826T>G (p.Ser276Ala) c.2020T>G (p.Ser674Ala) | |
9 | g.91724465A>G | CA373796451 | ROR2 | c.2029T>C (p.Ser677Pro) c.1609T>C (p.Ser537Pro) n.2497T>C c.826T>C (p.Ser276Pro) c.2020T>C (p.Ser674Pro) | COSMIC |
9 | g.91724465A>T | CA373796454 | ROR2 | c.2029T>A (p.Ser677Thr) c.1609T>A (p.Ser537Thr) n.2497T>A c.826T>A (p.Ser276Thr) c.2020T>A (p.Ser674Thr) | |
9 | g.91724466C>A | CA373796455 | ROR2 | c.2028G>T (p.Trp676Cys) c.1608G>T (p.Trp536Cys) n.2496G>T c.825G>T (p.Trp275Cys) c.2019G>T (p.Trp673Cys) | |
9 | g.91724466C>G | CA373796460 | ROR2 | c.2028G>C (p.Trp676Cys) c.1608G>C (p.Trp536Cys) n.2496G>C c.825G>C (p.Trp275Cys) c.2019G>C (p.Trp673Cys) | |
9 | g.91724466C>T | CA373796462 | ROR2 | c.2028G>A (p.Trp676Ter) c.1608G>A (p.Trp536Ter) n.2496G>A c.825G>A (p.Trp275Ter) c.2019G>A (p.Trp673Ter) | |
9 | g.91724467C>A | CA373796466 | ROR2 | c.2027G>T (p.Trp676Leu) c.1607G>T (p.Trp536Leu) n.2495G>T c.824G>T (p.Trp275Leu) c.2018G>T (p.Trp673Leu) | |
9 | g.91724467C>G | CA373796463 | ROR2 | c.2027G>C (p.Trp676Ser) c.1607G>C (p.Trp536Ser) n.2495G>C c.824G>C (p.Trp275Ser) c.2018G>C (p.Trp673Ser) | |
9 | g.91724467C>T | CA373796465 | ROR2 | c.2027G>A (p.Trp676Ter) c.1607G>A (p.Trp536Ter) n.2495G>A c.824G>A (p.Trp275Ter) c.2018G>A (p.Trp673Ter) | gnomAD v4 |
9 | g.91724468A>C | CA373796470 | ROR2 | c.2026T>G (p.Trp676Gly) c.1606T>G (p.Trp536Gly) n.2494T>G c.823T>G (p.Trp275Gly) c.2017T>G (p.Trp673Gly) | |
9 | g.91724468A>G | CA373796475 | ROR2 | c.2026T>C (p.Trp676Arg) c.1606T>C (p.Trp536Arg) n.2494T>C c.823T>C (p.Trp275Arg) c.2017T>C (p.Trp673Arg) | |
9 | g.91724468A>T | CA373796476 | ROR2 | c.2026T>A (p.Trp676Arg) c.1606T>A (p.Trp536Arg) n.2494T>A c.823T>A (p.Trp275Arg) c.2017T>A (p.Trp673Arg) | |
9 | g.91724469G>A | CA466339074 | ROR2 | c.2025C>T (p.Ile675=) c.1605C>T (p.Ile535=) n.2493C>T c.822C>T (p.Ile274=) c.2016C>T (p.Ile672=) | |
9 | g.91724469G>C | CA373796478 | ROR2 | c.2025C>G (p.Ile675Met) c.1605C>G (p.Ile535Met) n.2493C>G c.822C>G (p.Ile274Met) c.2016C>G (p.Ile672Met) | |
9 | g.91724469G>T | CA466339072 | ROR2 | c.2025C>A (p.Ile675=) c.1605C>A (p.Ile535=) n.2493C>A c.822C>A (p.Ile274=) c.2016C>A (p.Ile672=) | |
9 | g.91724470A>C | CA373796479 | ROR2 | c.2024T>G (p.Ile675Ser) c.1604T>G (p.Ile535Ser) n.2492T>G c.821T>G (p.Ile274Ser) c.2015T>G (p.Ile672Ser) | |
9 | g.91724470A>G | CA373796480 | ROR2 | c.2024T>C (p.Ile675Thr) c.1604T>C (p.Ile535Thr) n.2492T>C c.821T>C (p.Ile274Thr) c.2015T>C (p.Ile672Thr) | |
9 | g.91724470A>T | CA373796483 | ROR2 | c.2024T>A (p.Ile675Asn) c.1604T>A (p.Ile535Asn) n.2492T>A c.821T>A (p.Ile274Asn) c.2015T>A (p.Ile672Asn) | |
9 | g.91724471T>A | CA373796485 | ROR2 | c.2023A>T (p.Ile675Phe) c.1603A>T (p.Ile535Phe) n.2491A>T c.820A>T (p.Ile274Phe) c.2014A>T (p.Ile672Phe) | |
9 | g.91724471T>C | CA373796488 | ROR2 | c.2023A>G (p.Ile675Val) c.1603A>G (p.Ile535Val) n.2491A>G c.820A>G (p.Ile274Val) c.2014A>G (p.Ile672Val) | dbSNP gnomAD v3 gnomAD v4 |
9 | g.91724471T>G | CA373796493 | ROR2 | c.2023A>C (p.Ile675Leu) c.1603A>C (p.Ile535Leu) n.2491A>C c.820A>C (p.Ile274Leu) c.2014A>C (p.Ile672Leu) | |
9 | g.91724471T= | CA1863922805 | ROR2 | c.2023A= (p.Ile675=) c.1603A= (p.Ile535=) n.2491A= c.820A= (p.Ile274=) c.2014A= (p.Ile672=) | |
9 | g.91724472G>A | CA5120505 | ROR2 | c.2022C>T (p.Asp674=) c.1602C>T (p.Asp534=) n.2490C>T c.819C>T (p.Asp273=) c.2013C>T (p.Asp671=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
9 | g.91724472G>C | CA373796496 | ROR2 | c.2022C>G (p.Asp674Glu) c.1602C>G (p.Asp534Glu) n.2490C>G c.819C>G (p.Asp273Glu) c.2013C>G (p.Asp671Glu) | |
9 | g.91724472G= | CA1863922808 | ROR2 | c.2022C= (p.Asp674=) c.1602C= (p.Asp534=) n.2490C= c.819C= (p.Asp273=) c.2013C= (p.Asp671=) | |
9 | g.91724472G>T | CA373796499 | ROR2 | c.2022C>A (p.Asp674Glu) c.1602C>A (p.Asp534Glu) n.2490C>A c.819C>A (p.Asp273Glu) c.2013C>A (p.Asp671Glu) | COSMIC |
9 | g.91724473T>A | CA373796504 | ROR2 | c.2021A>T (p.Asp674Val) c.1601A>T (p.Asp534Val) n.2489A>T c.818A>T (p.Asp273Val) c.2012A>T (p.Asp671Val) | |
9 | g.91724473T>C | CA373796503 | ROR2 | c.2021A>G (p.Asp674Gly) c.1601A>G (p.Asp534Gly) n.2489A>G c.818A>G (p.Asp273Gly) c.2012A>G (p.Asp671Gly) | |
9 | g.91724473T>G | CA373796501 | ROR2 | c.2021A>C (p.Asp674Ala) c.1601A>C (p.Asp534Ala) n.2489A>C c.818A>C (p.Asp273Ala) c.2012A>C (p.Asp671Ala) | |
9 | g.91724474C>A | CA373796505 | ROR2 | c.2020G>T (p.Asp674Tyr) c.1600G>T (p.Asp534Tyr) n.2488G>T c.817G>T (p.Asp273Tyr) c.2011G>T (p.Asp671Tyr) | |
9 | g.91724474C>G | CA373796507 | ROR2 | c.2020G>C (p.Asp674His) c.1600G>C (p.Asp534His) n.2488G>C c.817G>C (p.Asp273His) c.2011G>C (p.Asp671His) | |
9 | g.91724474C>T | CA373796510 | ROR2 | c.2020G>A (p.Asp674Asn) c.1600G>A (p.Asp534Asn) n.2488G>A c.817G>A (p.Asp273Asn) c.2011G>A (p.Asp671Asn) | |
9 | g.91724475T>A | CA466339076 | ROR2 | c.2019A>T (p.Ser673=) c.1599A>T (p.Ser533=) n.2487A>T c.816A>T (p.Ser272=) c.2010A>T (p.Ser670=) | |
9 | g.91724475T>C | CA466339080 | ROR2 | c.2019A>G (p.Ser673=) c.1599A>G (p.Ser533=) n.2487A>G c.816A>G (p.Ser272=) c.2010A>G (p.Ser670=) | |
9 | g.91724475T>G | CA466339078 | ROR2 | c.2019A>C (p.Ser673=) c.1599A>C (p.Ser533=) n.2487A>C c.816A>C (p.Ser272=) c.2010A>C (p.Ser670=) | |
9 | g.91724476G>A | CA373796513 | ROR2 | c.2018C>T (p.Ser673Leu) c.1598C>T (p.Ser533Leu) n.2486C>T c.815C>T (p.Ser272Leu) c.2009C>T (p.Ser670Leu) | |
9 | g.91724476G>C | CA373796515 | ROR2 | c.2018C>G (p.Ser673Ter) c.1598C>G (p.Ser533Ter) n.2486C>G c.815C>G (p.Ser272Ter) c.2009C>G (p.Ser670Ter) | COSMIC |
9 | g.91724476G>T | CA373796517 | ROR2 | c.2018C>A (p.Ser673Ter) c.1598C>A (p.Ser533Ter) n.2486C>A c.815C>A (p.Ser272Ter) c.2009C>A (p.Ser670Ter) | |
9 | g.91724477A>C | CA373796520 | ROR2 | c.2017T>G (p.Ser673Ala) c.1597T>G (p.Ser533Ala) n.2485T>G c.814T>G (p.Ser272Ala) c.2008T>G (p.Ser670Ala) | |
9 | g.91724477A>G | CA373796521 | ROR2 | c.2017T>C (p.Ser673Pro) c.1597T>C (p.Ser533Pro) n.2485T>C c.814T>C (p.Ser272Pro) c.2008T>C (p.Ser670Pro) | |
9 | g.91724477A>T | CA373796524 | ROR2 | c.2017T>A (p.Ser673Thr) c.1597T>A (p.Ser533Thr) n.2485T>A c.814T>A (p.Ser272Thr) c.2008T>A (p.Ser670Thr) | |
9 | g.91724478G>A | CA466339082 | ROR2 | c.2016C>T (p.Asp672=) c.1596C>T (p.Asp532=) n.2484C>T c.813C>T (p.Asp271=) c.2007C>T (p.Asp669=) | gnomAD v4 |
9 | g.91724478G>C | CA373796526 | ROR2 | c.2016C>G (p.Asp672Glu) c.1596C>G (p.Asp532Glu) n.2484C>G c.813C>G (p.Asp271Glu) c.2007C>G (p.Asp669Glu) | |
9 | g.91724478G>T | CA373796529 | ROR2 | c.2016C>A (p.Asp672Glu) c.1596C>A (p.Asp532Glu) n.2484C>A c.813C>A (p.Asp271Glu) c.2007C>A (p.Asp669Glu) | |
9 | g.91724479T>A | CA373796531 | ROR2 | c.2015A>T (p.Asp672Val) c.1595A>T (p.Asp532Val) n.2483A>T c.812A>T (p.Asp271Val) c.2006A>T (p.Asp669Val) | |
9 | g.91724479T>C | CA373796533 | ROR2 | c.2015A>G (p.Asp672Gly) c.1595A>G (p.Asp532Gly) n.2483A>G c.812A>G (p.Asp271Gly) c.2006A>G (p.Asp669Gly) | dbSNP |
9 | g.91724479T>G | CA373796535 | ROR2 | c.2015A>C (p.Asp672Ala) c.1595A>C (p.Asp532Ala) n.2483A>C c.812A>C (p.Asp271Ala) c.2006A>C (p.Asp669Ala) | |
9 | g.91724479T= | CA1863922812 | ROR2 | c.2015A= (p.Asp672=) c.1595A= (p.Asp532=) n.2483A= c.812A= (p.Asp271=) c.2006A= (p.Asp669=) | |
9 | g.91724480C>A | CA373796540 | ROR2 | c.2014G>T (p.Asp672Tyr) c.1594G>T (p.Asp532Tyr) n.2482G>T c.811G>T (p.Asp271Tyr) c.2005G>T (p.Asp669Tyr) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
9 | g.91724480C= | CA1863922815 | ROR2 | c.2014G= (p.Asp672=) c.1594G= (p.Asp532=) n.2482G= c.811G= (p.Asp271=) c.2005G= (p.Asp669=) | |
9 | g.91724480C>G | CA5120507 | ROR2 | c.2014G>C (p.Asp672His) c.1594G>C (p.Asp532His) n.2482G>C c.811G>C (p.Asp271His) c.2005G>C (p.Asp669His) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.91724480C>T | CA5120506 | ROR2 | c.2014G>A (p.Asp672Asn) c.1594G>A (p.Asp532Asn) n.2482G>A c.811G>A (p.Asp271Asn) c.2005G>A (p.Asp669Asn) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
9 | g.91724481G>A | CA195323033 | ROR2 | c.2013C>T (p.Ile671=) c.1593C>T (p.Ile531=) n.2481C>T c.810C>T (p.Ile270=) c.2004C>T (p.Ile668=) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.91724481G>C | CA373796542 | ROR2 | c.2013C>G (p.Ile671Met) c.1593C>G (p.Ile531Met) n.2481C>G c.810C>G (p.Ile270Met) c.2004C>G (p.Ile668Met) | |
9 | g.91724481G= | CA1863922821 | ROR2 | c.2013C= (p.Ile671=) c.1593C= (p.Ile531=) n.2481C= c.810C= (p.Ile270=) c.2004C= (p.Ile668=) | |
9 | g.91724481G>T | CA466339085 | ROR2 | c.2013C>A (p.Ile671=) c.1593C>A (p.Ile531=) n.2481C>A c.810C>A (p.Ile270=) c.2004C>A (p.Ile668=) | |
9 | g.91724482A>C | CA373796545 | ROR2 | c.2012T>G (p.Ile671Ser) c.1592T>G (p.Ile531Ser) n.2480T>G c.809T>G (p.Ile270Ser) c.2003T>G (p.Ile668Ser) | |
9 | g.91724482A>G | CA373796549 | ROR2 | c.2012T>C (p.Ile671Thr) c.1592T>C (p.Ile531Thr) n.2480T>C c.809T>C (p.Ile270Thr) c.2003T>C (p.Ile668Thr) | |
9 | g.91724482A>T | CA373796550 | ROR2 | c.2012T>A (p.Ile671Asn) c.1592T>A (p.Ile531Asn) n.2480T>A c.809T>A (p.Ile270Asn) c.2003T>A (p.Ile668Asn) | |
9 | g.91724483T>A | CA373796552 | ROR2 | c.2011A>T (p.Ile671Phe) c.1591A>T (p.Ile531Phe) n.2479A>T c.808A>T (p.Ile270Phe) c.2002A>T (p.Ile668Phe) | |
9 | g.91724483T>C | CA373796554 | ROR2 | c.2011A>G (p.Ile671Val) c.1591A>G (p.Ile531Val) n.2479A>G c.808A>G (p.Ile270Val) c.2002A>G (p.Ile668Val) | gnomAD v4 |
9 | g.91724483T>G | CA373796557 | ROR2 | c.2011A>C (p.Ile671Leu) c.1591A>C (p.Ile531Leu) n.2479A>C c.808A>C (p.Ile270Leu) c.2002A>C (p.Ile668Leu) | |
9 | g.91724484G>A | CA466339087 | ROR2 | c.2010C>T (p.Ser670=) c.1590C>T (p.Ser530=) n.2478C>T c.807C>T (p.Ser269=) c.2001C>T (p.Ser667=) | gnomAD v4 |
9 | g.91724484G>C | CA466339088 | ROR2 | c.2010C>G (p.Ser670=) c.1590C>G (p.Ser530=) n.2478C>G c.807C>G (p.Ser269=) c.2001C>G (p.Ser667=) | |
9 | g.91724484G>T | CA466339089 | ROR2 | c.2010C>A (p.Ser670=) c.1590C>A (p.Ser530=) n.2478C>A c.807C>A (p.Ser269=) c.2001C>A (p.Ser667=) | |
9 | g.91724485G>A | CA373796564 | ROR2 | c.2009C>T (p.Ser670Phe) c.1589C>T (p.Ser530Phe) n.2477C>T c.806C>T (p.Ser269Phe) c.2000C>T (p.Ser667Phe) | |
9 | g.91724485G>C | CA373796561 | ROR2 | c.2009C>G (p.Ser670Cys) c.1589C>G (p.Ser530Cys) n.2477C>G c.806C>G (p.Ser269Cys) c.2000C>G (p.Ser667Cys) | |
9 | g.91724485G>T | CA373796562 | ROR2 | c.2009C>A (p.Ser670Tyr) c.1589C>A (p.Ser530Tyr) n.2477C>A c.806C>A (p.Ser269Tyr) c.2000C>A (p.Ser667Tyr) | |
9 | g.91724486A= | CA1863922827 | ROR2 | c.2008T= (p.Ser670=) c.1588T= (p.Ser530=) n.2476T= c.805T= (p.Ser269=) c.1999T= (p.Ser667=) | |
9 | g.91724486A>C | CA373796568 | ROR2 | c.2008T>G (p.Ser670Ala) c.1588T>G (p.Ser530Ala) n.2476T>G c.805T>G (p.Ser269Ala) c.1999T>G (p.Ser667Ala) | |
9 | g.91724486A>G | CA5120508 | ROR2 | c.2008T>C (p.Ser670Pro) c.1588T>C (p.Ser530Pro) n.2476T>C c.805T>C (p.Ser269Pro) c.1999T>C (p.Ser667Pro) | dbSNP ExAC gnomAD v2 |
9 | g.91724486A>T | CA373796570 | ROR2 | c.2008T>A (p.Ser670Thr) c.1588T>A (p.Ser530Thr) n.2476T>A c.805T>A (p.Ser269Thr) c.1999T>A (p.Ser667Thr) | |
9 | g.91724487G>A | CA466339092 | ROR2 | c.2007C>T (p.Phe669=) c.1587C>T (p.Phe529=) n.2475C>T c.804C>T (p.Phe268=) c.1998C>T (p.Phe666=) | |
9 | g.91724487G>C | CA373796573 | ROR2 | c.2007C>G (p.Phe669Leu) c.1587C>G (p.Phe529Leu) n.2475C>G c.804C>G (p.Phe268Leu) c.1998C>G (p.Phe666Leu) | dbSNP gnomAD v4 |
9 | g.91724487G= | CA1863922830 | ROR2 | c.2007C= (p.Phe669=) c.1587C= (p.Phe529=) n.2475C= c.804C= (p.Phe268=) c.1998C= (p.Phe666=) | |
9 | g.91724487G>T | CA373796577 | ROR2 | c.2007C>A (p.Phe669Leu) c.1587C>A (p.Phe529Leu) n.2475C>A c.804C>A (p.Phe268Leu) c.1998C>A (p.Phe666Leu) | |
9 | g.91724488A= | CA1863922834 | ROR2 | c.2006T= (p.Phe669=) c.1586T= (p.Phe529=) n.2474T= c.803T= (p.Phe268=) c.1997T= (p.Phe666=) | |
9 | g.91724488A>C | CA373796579 | ROR2 | c.2006T>G (p.Phe669Cys) c.1586T>G (p.Phe529Cys) n.2474T>G c.803T>G (p.Phe268Cys) c.1997T>G (p.Phe666Cys) | |
9 | g.91724488A>G | CA5120509 | ROR2 | c.2006T>C (p.Phe669Ser) c.1586T>C (p.Phe529Ser) n.2474T>C c.803T>C (p.Phe268Ser) c.1997T>C (p.Phe666Ser) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.91724488A>T | CA373796580 | ROR2 | c.2006T>A (p.Phe669Tyr) c.1586T>A (p.Phe529Tyr) n.2474T>A c.803T>A (p.Phe268Tyr) c.1997T>A (p.Phe666Tyr) | |
9 | g.91724488_91724489insCATGT | CA2690632332 | ROR2 | c.2005_2006insACATG (p.Phe669TyrfsTer?) c.1585_1586insACATG (p.Phe529TyrfsTer?) n.2473_2474insACATG c.802_803insACATG (p.Phe268TyrfsTer?) c.1996_1997insACATG (p.Phe666TyrfsTer?) | gnomAD v4 |
9 | g.91724489A>C | CA373796583 | ROR2 | c.2005T>G (p.Phe669Val) c.1585T>G (p.Phe529Val) n.2473T>G c.802T>G (p.Phe268Val) c.1996T>G (p.Phe666Val) | |
9 | g.91724489A>G | CA373796586 | ROR2 | c.2005T>C (p.Phe669Leu) c.1585T>C (p.Phe529Leu) n.2473T>C c.802T>C (p.Phe268Leu) c.1996T>C (p.Phe666Leu) | |
9 | g.91724489A>T | CA373796587 | ROR2 | c.2005T>A (p.Phe669Ile) c.1585T>A (p.Phe529Ile) n.2473T>A c.802T>A (p.Phe268Ile) c.1996T>A (p.Phe666Ile) | |
9 | g.91724490C>A | CA373796588 | ROR2 | c.2004G>T (p.Lys668Asn) c.1584G>T (p.Lys528Asn) n.2472G>T c.801G>T (p.Lys267Asn) c.1995G>T (p.Lys665Asn) | |
9 | g.91724490C= | CA1863922837 | ROR2 | c.2004G= (p.Lys668=) c.1584G= (p.Lys528=) n.2472G= c.801G= (p.Lys267=) c.1995G= (p.Lys665=) | |
9 | g.91724490C>G | CA195323040 | ROR2 | c.2004G>C (p.Lys668Asn) c.1584G>C (p.Lys528Asn) n.2472G>C c.801G>C (p.Lys267Asn) c.1995G>C (p.Lys665Asn) | dbSNP gnomAD v4 |
9 | g.91724490C>T | CA466339094 | ROR2 | c.2004G>A (p.Lys668=) c.1584G>A (p.Lys528=) n.2472G>A c.801G>A (p.Lys267=) c.1995G>A (p.Lys665=) | gnomAD v4 COSMIC |
9 | g.91724490_91724491insG | CA2690632339 | ROR2 | c.2003_2004insC (p.Lys668AsnfsTer?) c.1583_1584insC (p.Lys528AsnfsTer?) n.2471_2472insC c.800_801insC (p.Lys267AsnfsTer?) c.1994_1995insC (p.Lys665AsnfsTer?) | gnomAD v4 |
9 | g.91724491T>A | CA373796593 | ROR2 | c.2003A>T (p.Lys668Met) c.1583A>T (p.Lys528Met) n.2471A>T c.800A>T (p.Lys267Met) c.1994A>T (p.Lys665Met) | gnomAD v4 |
9 | g.91724491T>C | CA373796594 | ROR2 | c.2003A>G (p.Lys668Arg) c.1583A>G (p.Lys528Arg) n.2471A>G c.800A>G (p.Lys267Arg) c.1994A>G (p.Lys665Arg) | gnomAD v4 |
9 | g.91724491T>G | CA5120510 | ROR2 | c.2003A>C (p.Lys668Thr) c.1583A>C (p.Lys528Thr) n.2471A>C c.800A>C (p.Lys267Thr) c.1994A>C (p.Lys665Thr) | dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC |
9 | g.91724491T= | CA1863922841 | ROR2 | c.2003A= (p.Lys668=) c.1583A= (p.Lys528=) n.2471A= c.800A= (p.Lys267=) c.1994A= (p.Lys665=) | |
9 | g.91724492T>A | CA373796597 | ROR2 | c.2002A>T (p.Lys668Ter) c.1582A>T (p.Lys528Ter) n.2470A>T c.799A>T (p.Lys267Ter) c.1993A>T (p.Lys665Ter) | |
9 | g.91724492T>C | CA373796599 | ROR2 | c.2002A>G (p.Lys668Glu) c.1582A>G (p.Lys528Glu) n.2470A>G c.799A>G (p.Lys267Glu) c.1993A>G (p.Lys665Glu) | COSMIC |
9 | g.91724492T>G | CA373796601 | ROR2 | c.2002A>C (p.Lys668Gln) c.1582A>C (p.Lys528Gln) n.2470A>C c.799A>C (p.Lys267Gln) c.1993A>C (p.Lys665Gln) | |
9 | g.91724493G>A | CA466339095 | ROR2 | c.2001C>T (p.Gly667=) c.1581C>T (p.Gly527=) n.2469C>T c.798C>T (p.Gly266=) c.1992C>T (p.Gly664=) | |
9 | g.91724493G>C | CA466339096 | ROR2 | c.2001C>G (p.Gly667=) c.1581C>G (p.Gly527=) n.2469C>G c.798C>G (p.Gly266=) c.1992C>G (p.Gly664=) | |
9 | g.91724493G>T | CA466339099 | ROR2 | c.2001C>A (p.Gly667=) c.1581C>A (p.Gly527=) n.2469C>A c.798C>A (p.Gly266=) c.1992C>A (p.Gly664=) | |
9 | g.91724494C>A | CA373796608 | ROR2 | c.2000G>T (p.Gly667Val) c.1580G>T (p.Gly527Val) n.2468G>T c.797G>T (p.Gly266Val) c.1991G>T (p.Gly664Val) | |
9 | g.91724494C= | CA1863922844 | ROR2 | c.2000G= (p.Gly667=) c.1580G= (p.Gly527=) n.2468G= c.797G= (p.Gly266=) c.1991G= (p.Gly664=) | |
9 | g.91724494C>G | CA373796604 | ROR2 | c.2000G>C (p.Gly667Ala) c.1580G>C (p.Gly527Ala) n.2468G>C c.797G>C (p.Gly266Ala) c.1991G>C (p.Gly664Ala) | |
9 | g.91724494C>T | CA373796606 | ROR2 | c.2000G>A (p.Gly667Asp) c.1580G>A (p.Gly527Asp) n.2468G>A c.797G>A (p.Gly266Asp) c.1991G>A (p.Gly664Asp) | dbSNP gnomAD v2 gnomAD v4 |
9 | g.91724495C>A | CA373796611 | ROR2 | c.1999G>T (p.Gly667Cys) c.1579G>T (p.Gly527Cys) n.2467G>T c.796G>T (p.Gly266Cys) c.1990G>T (p.Gly664Cys) | |
9 | g.91724495C= | CA1863922846 | ROR2 | c.1999G= (p.Gly667=) c.1579G= (p.Gly527=) n.2467G= c.796G= (p.Gly266=) c.1990G= (p.Gly664=) | |
9 | g.91724495C>G | CA373796613 | ROR2 | c.1999G>C (p.Gly667Arg) c.1579G>C (p.Gly527Arg) n.2467G>C c.796G>C (p.Gly266Arg) c.1990G>C (p.Gly664Arg) | dbSNP gnomAD v4 |
9 | g.91724495C>T | CA5120511 | ROR2 | c.1999G>A (p.Gly667Ser) c.1579G>A (p.Gly527Ser) n.2467G>A c.796G>A (p.Gly266Ser) c.1990G>A (p.Gly664Ser) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
9 | g.91724496G>A | CA5120512 | ROR2 | c.1998C>T (p.Tyr666=) c.1578C>T (p.Tyr526=) n.2466C>T c.795C>T (p.Tyr265=) c.1989C>T (p.Tyr663=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.91724496G>C | CA373796617 | ROR2 | c.1998C>G (p.Tyr666Ter) c.1578C>G (p.Tyr526Ter) n.2466C>G c.795C>G (p.Tyr265Ter) c.1989C>G (p.Tyr663Ter) | |
9 | g.91724496G= | CA1863922848 | ROR2 | c.1998C= (p.Tyr666=) c.1578C= (p.Tyr526=) n.2466C= c.795C= (p.Tyr265=) c.1989C= (p.Tyr663=) | |
9 | g.91724496G>T | CA373796620 | ROR2 | c.1998C>A (p.Tyr666Ter) c.1578C>A (p.Tyr526Ter) n.2466C>A c.795C>A (p.Tyr265Ter) c.1989C>A (p.Tyr663Ter) | |
9 | g.91724497T>A | CA373796622 | ROR2 | c.1997A>T (p.Tyr666Phe) c.1577A>T (p.Tyr526Phe) n.2465A>T c.794A>T (p.Tyr265Phe) c.1988A>T (p.Tyr663Phe) | |
9 | g.91724497T>C | CA373796623 | ROR2 | c.1997A>G (p.Tyr666Cys) c.1577A>G (p.Tyr526Cys) n.2465A>G c.794A>G (p.Tyr265Cys) c.1988A>G (p.Tyr663Cys) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.91724497T>G | CA373796625 | ROR2 | c.1997A>C (p.Tyr666Ser) c.1577A>C (p.Tyr526Ser) n.2465A>C c.794A>C (p.Tyr265Ser) c.1988A>C (p.Tyr663Ser) | gnomAD v4 |
9 | g.91724497T= | CA1863922854 | ROR2 | c.1997A= (p.Tyr666=) c.1577A= (p.Tyr526=) n.2465A= c.794A= (p.Tyr265=) c.1988A= (p.Tyr663=) | |
9 | g.91724498A>C | CA373796626 | ROR2 | c.1996T>G (p.Tyr666Asp) c.1576T>G (p.Tyr526Asp) n.2464T>G c.793T>G (p.Tyr265Asp) c.1987T>G (p.Tyr663Asp) | |
9 | g.91724498A>G | CA373796627 | ROR2 | c.1996T>C (p.Tyr666His) c.1576T>C (p.Tyr526His) n.2464T>C c.793T>C (p.Tyr265His) c.1987T>C (p.Tyr663His) | |
9 | g.91724498A>T | CA373796629 | ROR2 | c.1996T>A (p.Tyr666Asn) c.1576T>A (p.Tyr526Asn) n.2464T>A c.793T>A (p.Tyr265Asn) c.1987T>A (p.Tyr663Asn) | |
9 | g.91724499C>A | CA5120513 | ROR2 | c.1995G>T (p.Met665Ile) c.1575G>T (p.Met525Ile) n.2463G>T c.792G>T (p.Met264Ile) c.1986G>T (p.Met662Ile) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.91724499C= | CA1863922864 | ROR2 | c.1995G= (p.Met665=) c.1575G= (p.Met525=) n.2463G= c.792G= (p.Met264=) c.1986G= (p.Met662=) | |
9 | g.91724499C>G | CA5120515 | ROR2 | c.1995G>C (p.Met665Ile) c.1575G>C (p.Met525Ile) n.2463G>C c.792G>C (p.Met264Ile) c.1986G>C (p.Met662Ile) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
9 | g.91724499C>T | CA5120514 | ROR2 | c.1995G>A (p.Met665Ile) c.1575G>A (p.Met525Ile) n.2463G>A c.792G>A (p.Met264Ile) c.1986G>A (p.Met662Ile) | dbSNP ExAC gnomAD v2 gnomAD v4 |
9 | g.91724500A= | CA1863922870 | ROR2 | c.1994T= (p.Met665=) c.1574T= (p.Met525=) n.2462T= c.791T= (p.Met264=) c.1985T= (p.Met662=) | |
9 | g.91724500A>C | CA373796634 | ROR2 | c.1994T>G (p.Met665Arg) c.1574T>G (p.Met525Arg) n.2462T>G c.791T>G (p.Met264Arg) c.1985T>G (p.Met662Arg) | |
9 | g.91724500A>G | CA5120516 | ROR2 | c.1994T>C (p.Met665Thr) c.1574T>C (p.Met525Thr) n.2462T>C c.791T>C (p.Met264Thr) c.1985T>C (p.Met662Thr) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.91724500A>T | CA373796636 | ROR2 | c.1994T>A (p.Met665Lys) c.1574T>A (p.Met525Lys) n.2462T>A c.791T>A (p.Met264Lys) c.1985T>A (p.Met662Lys) | |
9 | g.91724501T>A | CA373796639 | ROR2 | c.1993A>T (p.Met665Leu) c.1573A>T (p.Met525Leu) n.2461A>T c.790A>T (p.Met264Leu) c.1984A>T (p.Met662Leu) | |
9 | g.91724501T>C | CA373796641 | ROR2 | c.1993A>G (p.Met665Val) c.1573A>G (p.Met525Val) n.2461A>G c.790A>G (p.Met264Val) c.1984A>G (p.Met662Val) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.91724501T>G | CA373796642 | ROR2 | c.1993A>C (p.Met665Leu) c.1573A>C (p.Met525Leu) n.2461A>C c.790A>C (p.Met264Leu) c.1984A>C (p.Met662Leu) | |
9 | g.91724501T= | CA1863922876 | ROR2 | c.1993A= (p.Met665=) c.1573A= (p.Met525=) n.2461A= c.790A= (p.Met264=) c.1984A= (p.Met662=) | |
9 | g.91724502G>A | CA466339106 | ROR2 | c.1992C>T (p.Ile664=) c.1572C>T (p.Ile524=) n.2460C>T c.789C>T (p.Ile263=) c.1983C>T (p.Ile661=) | ClinVar dbSNP gnomAD v4 COSMIC |
9 | g.91724502G>C | CA373796645 | ROR2 | c.1992C>G (p.Ile664Met) c.1572C>G (p.Ile524Met) n.2460C>G c.789C>G (p.Ile263Met) c.1983C>G (p.Ile661Met) | |
9 | g.91724502G>T | CA466339108 | ROR2 | c.1992C>A (p.Ile664=) c.1572C>A (p.Ile524=) n.2460C>A c.789C>A (p.Ile263=) c.1983C>A (p.Ile661=) | |
9 | g.91724503A>C | CA373796652 | ROR2 | c.1991T>G (p.Ile664Ser) c.1571T>G (p.Ile524Ser) n.2459T>G c.788T>G (p.Ile263Ser) c.1982T>G (p.Ile661Ser) | |
9 | g.91724503A>G | CA373796654 | ROR2 | c.1991T>C (p.Ile664Thr) c.1571T>C (p.Ile524Thr) n.2459T>C c.788T>C (p.Ile263Thr) c.1982T>C (p.Ile661Thr) | COSMIC |
9 | g.91724503A>T | CA373796656 | ROR2 | c.1991T>A (p.Ile664Asn) c.1571T>A (p.Ile524Asn) n.2459T>A c.788T>A (p.Ile263Asn) c.1982T>A (p.Ile661Asn) | |
9 | g.91724504T>A | CA373796659 | ROR2 | c.1990A>T (p.Ile664Phe) c.1570A>T (p.Ile524Phe) n.2458A>T c.787A>T (p.Ile263Phe) c.1981A>T (p.Ile661Phe) | gnomAD v4 |
9 | g.91724504T>C | CA373796660 | ROR2 | c.1990A>G (p.Ile664Val) c.1570A>G (p.Ile524Val) n.2458A>G c.787A>G (p.Ile263Val) c.1981A>G (p.Ile661Val) | |
9 | g.91724504T>G | CA373796662 | ROR2 | c.1990A>C (p.Ile664Leu) c.1570A>C (p.Ile524Leu) n.2458A>C c.787A>C (p.Ile263Leu) c.1981A>C (p.Ile661Leu) | |
9 | g.91724505G>A | CA466339110 | ROR2 | c.1989C>T (p.Ala663=) c.1569C>T (p.Ala523=) n.2457C>T c.786C>T (p.Ala262=) c.1980C>T (p.Ala660=) | dbSNP gnomAD v4 |
9 | g.91724505G>C | CA466339111 | ROR2 | c.1989C>G (p.Ala663=) c.1569C>G (p.Ala523=) n.2457C>G c.786C>G (p.Ala262=) c.1980C>G (p.Ala660=) | |
9 | g.91724505G>T | CA466339112 | ROR2 | c.1989C>A (p.Ala663=) c.1569C>A (p.Ala523=) n.2457C>A c.786C>A (p.Ala262=) c.1980C>A (p.Ala660=) | |
9 | g.91724506G>A | CA373796668 | ROR2 | c.1988C>T (p.Ala663Val) c.1568C>T (p.Ala523Val) n.2456C>T c.785C>T (p.Ala262Val) c.1979C>T (p.Ala660Val) | |
9 | g.91724506G>C | CA373796666 | ROR2 | c.1988C>G (p.Ala663Gly) c.1568C>G (p.Ala523Gly) n.2456C>G c.785C>G (p.Ala262Gly) c.1979C>G (p.Ala660Gly) | |
9 | g.91724506G>T | CA373796665 | ROR2 | c.1988C>A (p.Ala663Asp) c.1568C>A (p.Ala523Asp) n.2456C>A c.785C>A (p.Ala262Asp) c.1979C>A (p.Ala660Asp) | |
9 | g.91724507C>A | CA373796674 | ROR2 | c.1987G>T (p.Ala663Ser) c.1567G>T (p.Ala523Ser) n.2455G>T c.784G>T (p.Ala262Ser) c.1978G>T (p.Ala660Ser) | |
9 | g.91724507C>G | CA373796671 | ROR2 | c.1987G>C (p.Ala663Pro) c.1567G>C (p.Ala523Pro) n.2455G>C c.784G>C (p.Ala262Pro) c.1978G>C (p.Ala660Pro) | |
9 | g.91724507C>T | CA373796672 | ROR2 | c.1987G>A (p.Ala663Thr) c.1567G>A (p.Ala523Thr) n.2455G>A c.784G>A (p.Ala262Thr) c.1978G>A (p.Ala660Thr) | |
9 | g.91724508C>A | CA373796676 | ROR2 | c.1986G>T (p.Glu662Asp) c.1566G>T (p.Glu522Asp) n.2454G>T c.783G>T (p.Glu261Asp) c.1977G>T (p.Glu659Asp) | gnomAD v4 |
9 | g.91724508C= | CA1863922878 | ROR2 | c.1986G= (p.Glu662=) c.1566G= (p.Glu522=) n.2454G= c.783G= (p.Glu261=) c.1977G= (p.Glu659=) | |
9 | g.91724508C>G | CA373796679 | ROR2 | c.1986G>C (p.Glu662Asp) c.1566G>C (p.Glu522Asp) n.2454G>C c.783G>C (p.Glu261Asp) c.1977G>C (p.Glu659Asp) | |
9 | g.91724508C>T | CA466339116 | ROR2 | c.1986G>A (p.Glu662=) c.1566G>A (p.Glu522=) n.2454G>A c.783G>A (p.Glu261=) c.1977G>A (p.Glu659=) | dbSNP gnomAD v3 gnomAD v4 |
9 | g.91724509T>A | CA373796682 | ROR2 | c.1985A>T (p.Glu662Val) c.1565A>T (p.Glu522Val) n.2453A>T c.782A>T (p.Glu261Val) c.1976A>T (p.Glu659Val) | |
9 | g.91724509T>C | CA373796683 | ROR2 | c.1985A>G (p.Glu662Gly) c.1565A>G (p.Glu522Gly) n.2453A>G c.782A>G (p.Glu261Gly) c.1976A>G (p.Glu659Gly) | |
9 | g.91724509T>G | CA373796684 | ROR2 | c.1985A>C (p.Glu662Ala) c.1565A>C (p.Glu522Ala) n.2453A>C c.782A>C (p.Glu261Ala) c.1976A>C (p.Glu659Ala) | |
9 | g.91724510C>A | CA373796686 | ROR2 | c.1984G>T (p.Glu662Ter) c.1564G>T (p.Glu522Ter) n.2452G>T c.781G>T (p.Glu261Ter) c.1975G>T (p.Glu659Ter) | |
9 | g.91724510C>G | CA373796690 | ROR2 | c.1984G>C (p.Glu662Gln) c.1564G>C (p.Glu522Gln) n.2452G>C c.781G>C (p.Glu261Gln) c.1975G>C (p.Glu659Gln) | |
9 | g.91724510C>T | CA373796691 | ROR2 | c.1984G>A (p.Glu662Lys) c.1564G>A (p.Glu522Lys) n.2452G>A c.781G>A (p.Glu261Lys) c.1975G>A (p.Glu659Lys) | |
9 | g.91724511T>A | CA466339119 | ROR2 | c.1983A>T (p.Pro661=) c.1563A>T (p.Pro521=) n.2451A>T c.780A>T (p.Pro260=) c.1974A>T (p.Pro658=) | |
9 | g.91724511T>C | CA466339117 | ROR2 | c.1983A>G (p.Pro661=) c.1563A>G (p.Pro521=) n.2451A>G c.780A>G (p.Pro260=) c.1974A>G (p.Pro658=) | |
9 | g.91724511T>G | CA466339118 | ROR2 | c.1983A>C (p.Pro661=) c.1563A>C (p.Pro521=) n.2451A>C c.780A>C (p.Pro260=) c.1974A>C (p.Pro658=) | dbSNP |
9 | g.91724511T= | CA1863922881 | ROR2 | c.1983A= (p.Pro661=) c.1563A= (p.Pro521=) n.2451A= c.780A= (p.Pro260=) c.1974A= (p.Pro658=) | |
9 | g.91724512G>A | CA373796694 | ROR2 | c.1982C>T (p.Pro661Leu) c.1562C>T (p.Pro521Leu) n.2450C>T c.779C>T (p.Pro260Leu) c.1973C>T (p.Pro658Leu) | |
9 | g.91724512G>C | CA373796696 | ROR2 | c.1982C>G (p.Pro661Arg) c.1562C>G (p.Pro521Arg) n.2450C>G c.779C>G (p.Pro260Arg) c.1973C>G (p.Pro658Arg) | |
9 | g.91724512G>T | CA373796699 | ROR2 | c.1982C>A (p.Pro661Gln) c.1562C>A (p.Pro521Gln) n.2450C>A c.779C>A (p.Pro260Gln) c.1973C>A (p.Pro658Gln) | |
9 | g.91724515del | CA2839081194 | ROR2 | c.1982del (p.Pro661GlnfsTer?) c.1562del (p.Pro521GlnfsTer?) n.2450del c.779del (p.Pro260GlnfsTer?) c.1973del (p.Pro658GlnfsTer?) | |
9 | g.91724513G>A | CA373796706 | ROR2 | c.1981C>T (p.Pro661Ser) c.1561C>T (p.Pro521Ser) n.2449C>T c.778C>T (p.Pro260Ser) c.1972C>T (p.Pro658Ser) | |
9 | g.91724513G>C | CA373796702 | ROR2 | c.1981C>G (p.Pro661Ala) c.1561C>G (p.Pro521Ala) n.2449C>G c.778C>G (p.Pro260Ala) c.1972C>G (p.Pro658Ala) | |
9 | g.91724513G>T | CA373796705 | ROR2 | c.1981C>A (p.Pro661Thr) c.1561C>A (p.Pro521Thr) n.2449C>A c.778C>A (p.Pro260Thr) c.1972C>A (p.Pro658Thr) | |
9 | g.91724514G>A | CA466339121 | ROR2 | c.1980C>T (p.Ala660=) c.1560C>T (p.Ala520=) n.2448C>T c.777C>T (p.Ala259=) c.1971C>T (p.Ala657=) | dbSNP |
9 | g.91724514G>C | CA466339122 | ROR2 | c.1980C>G (p.Ala660=) c.1560C>G (p.Ala520=) n.2448C>G c.777C>G (p.Ala259=) c.1971C>G (p.Ala657=) | |
9 | g.91724514G= | CA1863922886 | ROR2 | c.1980C= (p.Ala660=) c.1560C= (p.Ala520=) n.2448C= c.777C= (p.Ala259=) c.1971C= (p.Ala657=) | |
9 | g.91724514G>T | CA466339123 | ROR2 | c.1980C>A (p.Ala660=) c.1560C>A (p.Ala520=) n.2448C>A c.777C>A (p.Ala259=) c.1971C>A (p.Ala657=) | |
9 | g.91724515G>A | CA373796709 | ROR2 | c.1979C>T (p.Ala660Val) c.1559C>T (p.Ala520Val) n.2447C>T c.776C>T (p.Ala259Val) c.1970C>T (p.Ala657Val) | |
9 | g.91724515G>C | CA373796710 | ROR2 | c.1979C>G (p.Ala660Gly) c.1559C>G (p.Ala520Gly) n.2447C>G c.776C>G (p.Ala259Gly) c.1970C>G (p.Ala657Gly) | |
9 | g.91724515G>T | CA373796711 | ROR2 | c.1979C>A (p.Ala660Asp) c.1559C>A (p.Ala520Asp) n.2447C>A c.776C>A (p.Ala259Asp) c.1970C>A (p.Ala657Asp) | |
9 | g.91724516C>A | CA373796712 | ROR2 | c.1978G>T (p.Ala660Ser) c.1558G>T (p.Ala520Ser) n.2446G>T c.775G>T (p.Ala259Ser) c.1969G>T (p.Ala657Ser) | |
9 | g.91724516C>G | CA373796715 | ROR2 | c.1978G>C (p.Ala660Pro) c.1558G>C (p.Ala520Pro) n.2446G>C c.775G>C (p.Ala259Pro) c.1969G>C (p.Ala657Pro) | |
9 | g.91724516C>T | CA373796717 | ROR2 | c.1978G>A (p.Ala660Thr) c.1558G>A (p.Ala520Thr) n.2446G>A c.775G>A (p.Ala259Thr) c.1969G>A (p.Ala657Thr) | |
9 | g.91724517C>A | CA373796720 | ROR2 | c.1977G>T (p.Met659Ile) c.1557G>T (p.Met519Ile) n.2445G>T c.774G>T (p.Met258Ile) c.1968G>T (p.Met656Ile) | |
9 | g.91724517C>G | CA373796721 | ROR2 | c.1977G>C (p.Met659Ile) c.1557G>C (p.Met519Ile) n.2445G>C c.774G>C (p.Met258Ile) c.1968G>C (p.Met656Ile) | |
9 | g.91724517C>T | CA373796723 | ROR2 | c.1977G>A (p.Met659Ile) c.1557G>A (p.Met519Ile) n.2445G>A c.774G>A (p.Met258Ile) c.1968G>A (p.Met656Ile) | |
9 | g.91724518A>C | CA373796727 | ROR2 | c.1976T>G (p.Met659Arg) c.1556T>G (p.Met519Arg) n.2444T>G c.773T>G (p.Met258Arg) c.1967T>G (p.Met656Arg) | |
9 | g.91724518A>G | CA373796729 | ROR2 | c.1976T>C (p.Met659Thr) c.1556T>C (p.Met519Thr) n.2444T>C c.773T>C (p.Met258Thr) c.1967T>C (p.Met656Thr) | |
9 | g.91724518A>T | CA373796731 | ROR2 | c.1976T>A (p.Met659Lys) c.1556T>A (p.Met519Lys) n.2444T>A c.773T>A (p.Met258Lys) c.1967T>A (p.Met656Lys) | |
9 | g.91724519T>A | CA373796735 | ROR2 | c.1975A>T (p.Met659Leu) c.1555A>T (p.Met519Leu) n.2443A>T c.772A>T (p.Met258Leu) c.1966A>T (p.Met656Leu) | |
9 | g.91724519T>C | CA373796743 | ROR2 | c.1975A>G (p.Met659Val) c.1555A>G (p.Met519Val) n.2443A>G c.772A>G (p.Met258Val) c.1966A>G (p.Met656Val) | gnomAD v4 COSMIC |
9 | g.91724519T>G | CA373796734 | ROR2 | c.1975A>C (p.Met659Leu) c.1555A>C (p.Met519Leu) n.2443A>C c.772A>C (p.Met258Leu) c.1966A>C (p.Met656Leu) | |
9 | g.91724520C>A | CA373796745 | ROR2 | c.1974G>T (p.Trp658Cys) c.1554G>T (p.Trp518Cys) n.2442G>T c.771G>T (p.Trp257Cys) c.1965G>T (p.Trp655Cys) | |
9 | g.91724520C>G | CA373796751 | ROR2 | c.1974G>C (p.Trp658Cys) c.1554G>C (p.Trp518Cys) n.2442G>C c.771G>C (p.Trp257Cys) c.1965G>C (p.Trp655Cys) | |
9 | g.91724520C>T | CA373796749 | ROR2 | c.1974G>A (p.Trp658Ter) c.1554G>A (p.Trp518Ter) n.2442G>A c.771G>A (p.Trp257Ter) c.1965G>A (p.Trp655Ter) | |
9 | g.91724521C>A | CA373796753 | ROR2 | c.1973G>T (p.Trp658Leu) c.1553G>T (p.Trp518Leu) n.2441G>T c.770G>T (p.Trp257Leu) c.1964G>T (p.Trp655Leu) | |
9 | g.91724521C>G | CA373796758 | ROR2 | c.1973G>C (p.Trp658Ser) c.1553G>C (p.Trp518Ser) n.2441G>C c.770G>C (p.Trp257Ser) c.1964G>C (p.Trp655Ser) | |
9 | g.91724521C>T | CA373796755 | ROR2 | c.1973G>A (p.Trp658Ter) c.1553G>A (p.Trp518Ter) n.2441G>A c.770G>A (p.Trp257Ter) c.1964G>A (p.Trp655Ter) | gnomAD v4 |
9 | g.91724522A>C | CA373796761 | ROR2 | c.1972T>G (p.Trp658Gly) c.1552T>G (p.Trp518Gly) n.2440T>G c.769T>G (p.Trp257Gly) c.1963T>G (p.Trp655Gly) | |
9 | g.91724522A>G | CA373796763 | ROR2 | c.1972T>C (p.Trp658Arg) c.1552T>C (p.Trp518Arg) n.2440T>C c.769T>C (p.Trp257Arg) c.1963T>C (p.Trp655Arg) | |
9 | g.91724522A>T | CA373796766 | ROR2 | c.1972T>A (p.Trp658Arg) c.1552T>A (p.Trp518Arg) n.2440T>A c.769T>A (p.Trp257Arg) c.1963T>A (p.Trp655Arg) | |
9 | g.91724523G>A | CA466339126 | ROR2 | c.1971C>T (p.Arg657=) c.1551C>T (p.Arg517=) n.2439C>T c.768C>T (p.Arg256=) c.1962C>T (p.Arg654=) | COSMIC |
9 | g.91724523G>C | CA466339127 | ROR2 | c.1971C>G (p.Arg657=) c.1551C>G (p.Arg517=) n.2439C>G c.768C>G (p.Arg256=) c.1962C>G (p.Arg654=) | |
9 | g.91724523G>T | CA466339128 | ROR2 | c.1971C>A (p.Arg657=) c.1551C>A (p.Arg517=) n.2439C>A c.768C>A (p.Arg256=) c.1962C>A (p.Arg654=) | |
9 | g.91724524C>A | CA373796769 | ROR2 | c.1970G>T (p.Arg657Leu) c.1550G>T (p.Arg517Leu) n.2438G>T c.767G>T (p.Arg256Leu) c.1961G>T (p.Arg654Leu) | gnomAD v4 |
9 | g.91724524C= | CA1863922889 | ROR2 | c.1970G= (p.Arg657=) c.1550G= (p.Arg517=) n.2438G= c.767G= (p.Arg256=) c.1961G= (p.Arg654=) | |
9 | g.91724524C>G | CA373796771 | ROR2 | c.1970G>C (p.Arg657Pro) c.1550G>C (p.Arg517Pro) n.2438G>C c.767G>C (p.Arg256Pro) c.1961G>C (p.Arg654Pro) | |
9 | g.91724524C>T | CA173318 | ROR2 | c.1970G>A (p.Arg657His) c.1550G>A (p.Arg517His) n.2438G>A c.767G>A (p.Arg256His) c.1961G>A (p.Arg654His) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.91724524_91724525insCT | CA1863922894 | ROR2 | c.1969_1970insAG (p.Arg657GlnfsTer?) c.1549_1550insAG (p.Arg517GlnfsTer?) n.2437_2438insAG c.766_767insAG (p.Arg256GlnfsTer?) c.1960_1961insAG (p.Arg654GlnfsTer?) | dbSNP |
9 | g.91724525G>A | CA5120517 | ROR2 | c.1969C>T (p.Arg657Cys) c.1549C>T (p.Arg517Cys) n.2437C>T c.766C>T (p.Arg256Cys) c.1960C>T (p.Arg654Cys) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC |
9 | g.91724525G>C | CA373796777 | ROR2 | c.1969C>G (p.Arg657Gly) c.1549C>G (p.Arg517Gly) n.2437C>G c.766C>G (p.Arg256Gly) c.1960C>G (p.Arg654Gly) | |
9 | g.91724525G= | CA1863922895 | ROR2 | c.1969C= (p.Arg657=) c.1549C= (p.Arg517=) n.2437C= c.766C= (p.Arg256=) c.1960C= (p.Arg654=) | |
9 | g.91724525G>T | CA373796779 | ROR2 | c.1969C>A (p.Arg657Ser) c.1549C>A (p.Arg517Ser) n.2437C>A c.766C>A (p.Arg256Ser) c.1960C>A (p.Arg654Ser) |