Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
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) | |
9 | g.91724526G>A | CA466339130 | ROR2 | c.1968C>T (p.Ile656=) c.1548C>T (p.Ile516=) n.2436C>T c.765C>T (p.Ile255=) c.1959C>T (p.Ile653=) | gnomAD v4 |
9 | g.91724526G>C | CA373796782 | ROR2 | c.1968C>G (p.Ile656Met) c.1548C>G (p.Ile516Met) n.2436C>G c.765C>G (p.Ile255Met) c.1959C>G (p.Ile653Met) | |
9 | g.91724526G= | CA1863922898 | ROR2 | c.1968C= (p.Ile656=) c.1548C= (p.Ile516=) n.2436C= c.765C= (p.Ile255=) c.1959C= (p.Ile653=) | |
9 | g.91724526G>T | CA466339131 | ROR2 | c.1968C>A (p.Ile656=) c.1548C>A (p.Ile516=) n.2436C>A c.765C>A (p.Ile255=) c.1959C>A (p.Ile653=) | dbSNP gnomAD v4 |
9 | g.91724527A>C | CA373796785 | ROR2 | c.1967T>G (p.Ile656Ser) c.1547T>G (p.Ile516Ser) n.2435T>G c.764T>G (p.Ile255Ser) c.1958T>G (p.Ile653Ser) | |
9 | g.91724527A>G | CA373796786 | ROR2 | c.1967T>C (p.Ile656Thr) c.1547T>C (p.Ile516Thr) n.2435T>C c.764T>C (p.Ile255Thr) c.1958T>C (p.Ile653Thr) | |
9 | g.91724527A>T | CA373796789 | ROR2 | c.1967T>A (p.Ile656Asn) c.1547T>A (p.Ile516Asn) n.2435T>A c.764T>A (p.Ile255Asn) c.1958T>A (p.Ile653Asn) | |
9 | g.91724528T>A | CA373796796 | ROR2 | c.1966A>T (p.Ile656Phe) c.1546A>T (p.Ile516Phe) n.2434A>T c.763A>T (p.Ile255Phe) c.1957A>T (p.Ile653Phe) | |
9 | g.91724528T>C | CA373796794 | ROR2 | c.1966A>G (p.Ile656Val) c.1546A>G (p.Ile516Val) n.2434A>G c.763A>G (p.Ile255Val) c.1957A>G (p.Ile653Val) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
9 | g.91724528T>G | CA373796792 | ROR2 | c.1966A>C (p.Ile656Leu) c.1546A>C (p.Ile516Leu) n.2434A>C c.763A>C (p.Ile255Leu) c.1957A>C (p.Ile653Leu) | |
9 | g.91724528T= | CA1863922900 | ROR2 | c.1966A= (p.Ile656=) c.1546A= (p.Ile516=) n.2434A= c.763A= (p.Ile255=) c.1957A= (p.Ile653=) | |
9 | g.91724529A>C | CA466339212 | ROR2 | c.1965T>G (p.Pro655=) c.1545T>G (p.Pro515=) n.2433T>G c.762T>G (p.Pro254=) c.1956T>G (p.Pro652=) | |
9 | g.91724529A>G | CA466339213 | ROR2 | c.1965T>C (p.Pro655=) c.1545T>C (p.Pro515=) n.2433T>C c.762T>C (p.Pro254=) c.1956T>C (p.Pro652=) | |
9 | g.91724529A>T | CA466339214 | ROR2 | c.1965T>A (p.Pro655=) c.1545T>A (p.Pro515=) n.2433T>A c.762T>A (p.Pro254=) c.1956T>A (p.Pro652=) | |
9 | g.91724530G>A | CA5120518 | ROR2 | c.1964C>T (p.Pro655Leu) c.1544C>T (p.Pro515Leu) n.2432C>T c.761C>T (p.Pro254Leu) c.1955C>T (p.Pro652Leu) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
9 | g.91724530G>C | CA373796798 | ROR2 | c.1964C>G (p.Pro655Arg) c.1544C>G (p.Pro515Arg) n.2432C>G c.761C>G (p.Pro254Arg) c.1955C>G (p.Pro652Arg) | |
9 | g.91724530G= | CA1863922904 | ROR2 | c.1964C= (p.Pro655=) c.1544C= (p.Pro515=) n.2432C= c.761C= (p.Pro254=) c.1955C= (p.Pro652=) | |
9 | g.91724530G>T | CA373796801 | ROR2 | c.1964C>A (p.Pro655His) c.1544C>A (p.Pro515His) n.2432C>A c.761C>A (p.Pro254His) c.1955C>A (p.Pro652His) | |
9 | g.91724531G>A | CA5120519 | ROR2 | c.1963C>T (p.Pro655Ser) c.1543C>T (p.Pro515Ser) n.2431C>T c.760C>T (p.Pro254Ser) c.1954C>T (p.Pro652Ser) | dbSNP ExAC gnomAD v2 gnomAD v4 |
9 | g.91724531G>C | CA373796804 | ROR2 | c.1963C>G (p.Pro655Ala) c.1543C>G (p.Pro515Ala) n.2431C>G c.760C>G (p.Pro254Ala) c.1954C>G (p.Pro652Ala) | |
9 | g.91724531G= | CA1863922906 | ROR2 | c.1963C= (p.Pro655=) c.1543C= (p.Pro515=) n.2431C= c.760C= (p.Pro254=) c.1954C= (p.Pro652=) | |
9 | g.91724531G>T | CA373796806 | ROR2 | c.1963C>A (p.Pro655Thr) c.1543C>A (p.Pro515Thr) n.2431C>A c.760C>A (p.Pro254Thr) c.1954C>A (p.Pro652Thr) | |
9 | g.91724531_91724545dup | CA2690632374 | ROR2 | c.1949_1963dup (p.Leu654_Pro655insArgAsnSerLeuLeu) c.1529_1543dup (p.Leu514_Pro515insArgAsnSerLeuLeu) n.2417_2431dup c.746_760dup (p.Leu253_Pro254insArgAsnSerLeuLeu) c.1940_1954dup (p.Leu651_Pro652insArgAsnSerLeuLeu) | gnomAD v4 |
9 | g.91724532C>A | CA466339218 | ROR2 | c.1962G>T (p.Leu654=) c.1542G>T (p.Leu514=) n.2430G>T c.759G>T (p.Leu253=) c.1953G>T (p.Leu651=) | |
9 | g.91724532C= | CA1863922908 | ROR2 | c.1962G= (p.Leu654=) c.1542G= (p.Leu514=) n.2430G= c.759G= (p.Leu253=) c.1953G= (p.Leu651=) | |
9 | g.91724532C>G | CA466339219 | ROR2 | c.1962G>C (p.Leu654=) c.1542G>C (p.Leu514=) n.2430G>C c.759G>C (p.Leu253=) c.1953G>C (p.Leu651=) | |
9 | g.91724532C>T | CA5120520 | ROR2 | c.1962G>A (p.Leu654=) c.1542G>A (p.Leu514=) n.2430G>A c.759G>A (p.Leu253=) c.1953G>A (p.Leu651=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.91724539_91724553del | CA2690632375 | ROR2 | c.1948_1962del (p.Gly650_Leu654del) c.1528_1542del (p.Gly510_Leu514del) n.2416_2430del c.745_759del (p.Gly249_Leu253del) c.1939_1953del (p.Gly647_Leu651del) | gnomAD v4 |
9 | g.91724533A>C | CA373796810 | ROR2 | c.1961T>G (p.Leu654Arg) c.1541T>G (p.Leu514Arg) n.2429T>G c.758T>G (p.Leu253Arg) c.1952T>G (p.Leu651Arg) | |
9 | g.91724533A>G | CA373796813 | ROR2 | c.1961T>C (p.Leu654Pro) c.1541T>C (p.Leu514Pro) n.2429T>C c.758T>C (p.Leu253Pro) c.1952T>C (p.Leu651Pro) | |
9 | g.91724533A>T | CA373796816 | ROR2 | c.1961T>A (p.Leu654Gln) c.1541T>A (p.Leu514Gln) n.2429T>A c.758T>A (p.Leu253Gln) c.1952T>A (p.Leu651Gln) | |
9 | g.91724534G>A | CA466339221 | ROR2 | c.1960C>T (p.Leu654=) c.1540C>T (p.Leu514=) n.2428C>T c.757C>T (p.Leu253=) c.1951C>T (p.Leu651=) | |
9 | g.91724534G>C | CA373796818 | ROR2 | c.1960C>G (p.Leu654Val) c.1540C>G (p.Leu514Val) n.2428C>G c.757C>G (p.Leu253Val) c.1951C>G (p.Leu651Val) | |
9 | g.91724534G>T | CA373796819 | ROR2 | c.1960C>A (p.Leu654Met) c.1540C>A (p.Leu514Met) n.2428C>A c.757C>A (p.Leu253Met) c.1951C>A (p.Leu651Met) | |
9 | g.91724535C>A | CA466339222 | ROR2 | c.1959G>T (p.Leu653=) c.1539G>T (p.Leu513=) n.2427G>T c.756G>T (p.Leu252=) c.1950G>T (p.Leu650=) | |
9 | g.91724535C= | CA1863922914 | ROR2 | c.1959G= (p.Leu653=) c.1539G= (p.Leu513=) n.2427G= c.756G= (p.Leu252=) c.1950G= (p.Leu650=) | |
9 | g.91724535C>G | CA466339223 | ROR2 | c.1959G>C (p.Leu653=) c.1539G>C (p.Leu513=) n.2427G>C c.756G>C (p.Leu252=) c.1950G>C (p.Leu650=) | |
9 | g.91724535C>T | CA272467 | ROR2 | c.1959G>A (p.Leu653=) c.1539G>A (p.Leu513=) n.2427G>A c.756G>A (p.Leu252=) c.1950G>A (p.Leu650=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.91724536A>C | CA373796823 | ROR2 | c.1958T>G (p.Leu653Arg) c.1538T>G (p.Leu513Arg) n.2426T>G c.755T>G (p.Leu252Arg) c.1949T>G (p.Leu650Arg) | |
9 | g.91724536A>G | CA373796825 | ROR2 | c.1958T>C (p.Leu653Pro) c.1538T>C (p.Leu513Pro) n.2426T>C c.755T>C (p.Leu252Pro) c.1949T>C (p.Leu650Pro) | |
9 | g.91724536A>T | CA373796822 | ROR2 | c.1958T>A (p.Leu653Gln) c.1538T>A (p.Leu513Gln) n.2426T>A c.755T>A (p.Leu252Gln) c.1949T>A (p.Leu650Gln) |