| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 9 | g.91724424C>A | CA466339025 | ROR2 | c.2070G>T (p.Leu690=) c.1650G>T (p.Leu550=) n.2538G>T c.867G>T (p.Leu289=) c.2061G>T (p.Leu687=) | |
| 9 | g.91724424C= | CA1863922758 | ROR2 | c.2070G= (p.Leu690=) c.1650G= (p.Leu550=) n.2538G= c.867G= (p.Leu289=) c.2061G= (p.Leu687=) | |
| 9 | g.91724424C>G | CA466339026 | ROR2 | c.2070G>C (p.Leu690=) c.1650G>C (p.Leu550=) n.2538G>C c.867G>C (p.Leu289=) c.2061G>C (p.Leu687=) | |
| 9 | g.91724424C>T | CA195322902 | ROR2 | c.2070G>A (p.Leu690=) c.1650G>A (p.Leu550=) n.2538G>A c.867G>A (p.Leu289=) c.2061G>A (p.Leu687=) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 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 |