Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
9 | g.91724328A= | CA1863922625 | ROR2 | c.2166T= (p.Tyr722=) c.1746T= (p.Tyr582=) n.2634T= c.963T= (p.Tyr321=) c.2157T= (p.Tyr719=) | |
9 | g.91724328A>C | CA373795684 | ROR2 | c.2166T>G (p.Tyr722Ter) c.1746T>G (p.Tyr582Ter) n.2634T>G c.963T>G (p.Tyr321Ter) c.2157T>G (p.Tyr719Ter) | |
9 | g.91724328A>G | CA5120470 | ROR2 | c.2166T>C (p.Tyr722=) c.1746T>C (p.Tyr582=) n.2634T>C c.963T>C (p.Tyr321=) c.2157T>C (p.Tyr719=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.91724328A>T | CA373795693 | ROR2 | c.2166T>A (p.Tyr722Ter) c.1746T>A (p.Tyr582Ter) n.2634T>A c.963T>A (p.Tyr321Ter) c.2157T>A (p.Tyr719Ter) | |
9 | g.91724329T>A | CA373795700 | ROR2 | c.2165A>T (p.Tyr722Phe) c.1745A>T (p.Tyr582Phe) n.2633A>T c.962A>T (p.Tyr321Phe) c.2156A>T (p.Tyr719Phe) | |
9 | g.91724329T>C | CA195322666 | ROR2 | c.2165A>G (p.Tyr722Cys) c.1745A>G (p.Tyr582Cys) n.2633A>G c.962A>G (p.Tyr321Cys) c.2156A>G (p.Tyr719Cys) | dbSNP gnomAD v4 |
9 | g.91724329T>G | CA373795702 | ROR2 | c.2165A>C (p.Tyr722Ser) c.1745A>C (p.Tyr582Ser) n.2633A>C c.962A>C (p.Tyr321Ser) c.2156A>C (p.Tyr719Ser) | |
9 | g.91724329T= | CA1863922628 | ROR2 | c.2165A= (p.Tyr722=) c.1745A= (p.Tyr582=) n.2633A= c.962A= (p.Tyr321=) c.2156A= (p.Tyr719=) | |
9 | g.91724330A>C | CA373795705 | ROR2 | c.2164T>G (p.Tyr722Asp) c.1744T>G (p.Tyr582Asp) n.2632T>G c.961T>G (p.Tyr321Asp) c.2155T>G (p.Tyr719Asp) | |
9 | g.91724330A>G | CA373795707 | ROR2 | c.2164T>C (p.Tyr722His) c.1744T>C (p.Tyr582His) n.2632T>C c.961T>C (p.Tyr321His) c.2155T>C (p.Tyr719His) | gnomAD v4 |
9 | g.91724330A>T | CA373795706 | ROR2 | c.2164T>A (p.Tyr722Asn) c.1744T>A (p.Tyr582Asn) n.2632T>A c.961T>A (p.Tyr321Asn) c.2155T>A (p.Tyr719Asn) | |
9 | g.91724331C>A | CA466338929 | ROR2 | c.2163G>T (p.Val721=) c.1743G>T (p.Val581=) n.2631G>T c.960G>T (p.Val320=) c.2154G>T (p.Val718=) | gnomAD v4 |
9 | g.91724331C= | CA1863922634 | ROR2 | c.2163G= (p.Val721=) c.1743G= (p.Val581=) n.2631G= c.960G= (p.Val320=) c.2154G= (p.Val718=) | |
9 | g.91724331C>G | CA466338931 | ROR2 | c.2163G>C (p.Val721=) c.1743G>C (p.Val581=) n.2631G>C c.960G>C (p.Val320=) c.2154G>C (p.Val718=) | |
9 | g.91724331C>T | CA466338930 | ROR2 | c.2163G>A (p.Val721=) c.1743G>A (p.Val581=) n.2631G>A c.960G>A (p.Val320=) c.2154G>A (p.Val718=) | dbSNP gnomAD v2 |
9 | g.91724332A= | CA1863922636 | ROR2 | c.2162T= (p.Val721=) c.1742T= (p.Val581=) n.2630T= c.959T= (p.Val320=) c.2153T= (p.Val718=) | |
9 | g.91724332A>C | CA195322706 | ROR2 | c.2162T>G (p.Val721Gly) c.1742T>G (p.Val581Gly) n.2630T>G c.959T>G (p.Val320Gly) c.2153T>G (p.Val718Gly) | dbSNP |
9 | g.91724332A>G | CA373795708 | ROR2 | c.2162T>C (p.Val721Ala) c.1742T>C (p.Val581Ala) n.2630T>C c.959T>C (p.Val320Ala) c.2153T>C (p.Val718Ala) | gnomAD v4 |
9 | g.91724332A>T | CA373795710 | ROR2 | c.2162T>A (p.Val721Glu) c.1742T>A (p.Val581Glu) n.2630T>A c.959T>A (p.Val320Glu) c.2153T>A (p.Val718Glu) | |
9 | g.91724333C>A | CA373795712 | ROR2 | c.2161G>T (p.Val721Leu) c.1741G>T (p.Val581Leu) n.2629G>T c.958G>T (p.Val320Leu) c.2152G>T (p.Val718Leu) | dbSNP |
9 | g.91724333C= | CA1863922638 | ROR2 | c.2161G= (p.Val721=) c.1741G= (p.Val581=) n.2629G= c.958G= (p.Val320=) c.2152G= (p.Val718=) | |
9 | g.91724333C>G | CA373795713 | ROR2 | c.2161G>C (p.Val721Leu) c.1741G>C (p.Val581Leu) n.2629G>C c.958G>C (p.Val320Leu) c.2152G>C (p.Val718Leu) | |
9 | g.91724333C>T | CA373795719 | ROR2 | c.2161G>A (p.Val721Met) c.1741G>A (p.Val581Met) n.2629G>A c.958G>A (p.Val320Met) c.2152G>A (p.Val718Met) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.91724334C>A | CA373795722 | ROR2 | c.2160G>T (p.Trp720Cys) c.1740G>T (p.Trp580Cys) n.2628G>T c.957G>T (p.Trp319Cys) c.2151G>T (p.Trp717Cys) | |
9 | g.91724334C= | CA1863922643 | ROR2 | c.2160G= (p.Trp720=) c.1740G= (p.Trp580=) n.2628G= c.957G= (p.Trp319=) c.2151G= (p.Trp717=) | |
9 | g.91724334C>G | CA373795724 | ROR2 | c.2160G>C (p.Trp720Cys) c.1740G>C (p.Trp580Cys) n.2628G>C c.957G>C (p.Trp319Cys) c.2151G>C (p.Trp717Cys) | |
9 | g.91724334C>T | CA254145 | ROR2 | c.2160G>A (p.Trp720Ter) c.1740G>A (p.Trp580Ter) n.2628G>A c.957G>A (p.Trp319Ter) c.2151G>A (p.Trp717Ter) | ClinVar dbSNP gnomAD v4 |
9 | g.91724335C>A | CA373795726 | ROR2 | c.2159G>T (p.Trp720Leu) c.1739G>T (p.Trp580Leu) n.2627G>T c.956G>T (p.Trp319Leu) c.2150G>T (p.Trp717Leu) | |
9 | g.91724335C>G | CA373795735 | ROR2 | c.2159G>C (p.Trp720Ser) c.1739G>C (p.Trp580Ser) n.2627G>C c.956G>C (p.Trp319Ser) c.2150G>C (p.Trp717Ser) | |
9 | g.91724335C>T | CA373795736 | ROR2 | c.2159G>A (p.Trp720Ter) c.1739G>A (p.Trp580Ter) n.2627G>A c.956G>A (p.Trp319Ter) c.2150G>A (p.Trp717Ter) | |
9 | g.91724336A= | CA1863922646 | ROR2 | c.2158T= (p.Trp720=) c.1738T= (p.Trp580=) n.2626T= c.955T= (p.Trp319=) c.2149T= (p.Trp717=) | |
9 | g.91724336A>C | CA373795740 | ROR2 | c.2158T>G (p.Trp720Gly) c.1738T>G (p.Trp580Gly) n.2626T>G c.955T>G (p.Trp319Gly) c.2149T>G (p.Trp717Gly) | dbSNP gnomAD v2 gnomAD v4 |
9 | g.91724336A>G | CA373795742 | ROR2 | c.2158T>C (p.Trp720Arg) c.1738T>C (p.Trp580Arg) n.2626T>C c.955T>C (p.Trp319Arg) c.2149T>C (p.Trp717Arg) | gnomAD v4 |
9 | g.91724336A>T | CA373795739 | ROR2 | c.2158T>A (p.Trp720Arg) c.1738T>A (p.Trp580Arg) n.2626T>A c.955T>A (p.Trp319Arg) c.2149T>A (p.Trp717Arg) | |
9 | g.91724337G>A | CA466338935 | ROR2 | c.2157C>T (p.Ala719=) c.1737C>T (p.Ala579=) n.2625C>T c.954C>T (p.Ala318=) c.2148C>T (p.Ala716=) | |
9 | g.91724337G>C | CA466338936 | ROR2 | c.2157C>G (p.Ala719=) c.1737C>G (p.Ala579=) n.2625C>G c.954C>G (p.Ala318=) c.2148C>G (p.Ala716=) | |
9 | g.91724337G>T | CA466338937 | ROR2 | c.2157C>A (p.Ala719=) c.1737C>A (p.Ala579=) n.2625C>A c.954C>A (p.Ala318=) c.2148C>A (p.Ala716=) | gnomAD v4 |
9 | g.91724338G>A | CA373795746 | ROR2 | c.2156C>T (p.Ala719Val) c.1736C>T (p.Ala579Val) n.2624C>T c.953C>T (p.Ala318Val) c.2147C>T (p.Ala716Val) | gnomAD v4 COSMIC |
9 | g.91724338G>C | CA373795743 | ROR2 | c.2156C>G (p.Ala719Gly) c.1736C>G (p.Ala579Gly) n.2624C>G c.953C>G (p.Ala318Gly) c.2147C>G (p.Ala716Gly) | |
9 | g.91724338G>T | CA373795744 | ROR2 | c.2156C>A (p.Ala719Asp) c.1736C>A (p.Ala579Asp) n.2624C>A c.953C>A (p.Ala318Asp) c.2147C>A (p.Ala716Asp) | gnomAD v4 |
9 | g.91724339C>A | CA373795748 | ROR2 | c.2155G>T (p.Ala719Ser) c.1735G>T (p.Ala579Ser) n.2623G>T c.952G>T (p.Ala318Ser) c.2146G>T (p.Ala716Ser) | gnomAD v4 |
9 | g.91724339C= | CA1863922651 | ROR2 | c.2155G= (p.Ala719=) c.1735G= (p.Ala579=) n.2623G= c.952G= (p.Ala318=) c.2146G= (p.Ala716=) | |
9 | g.91724339C>G | CA5120472 | ROR2 | c.2155G>C (p.Ala719Pro) c.1735G>C (p.Ala579Pro) n.2623G>C c.952G>C (p.Ala318Pro) c.2146G>C (p.Ala716Pro) | dbSNP ExAC gnomAD v2 gnomAD v4 |
9 | g.91724339C>T | CA5120471 | ROR2 | c.2155G>A (p.Ala719Thr) c.1735G>A (p.Ala579Thr) n.2623G>A c.952G>A (p.Ala318Thr) c.2146G>A (p.Ala716Thr) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
9 | g.91724340G>A | CA173324 | ROR2 | c.2154C>T (p.Pro718=) c.1734C>T (p.Pro578=) n.2622C>T c.951C>T (p.Pro317=) c.2145C>T (p.Pro715=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.91724340G>C | CA466338939 | ROR2 | c.2154C>G (p.Pro718=) c.1734C>G (p.Pro578=) n.2622C>G c.951C>G (p.Pro317=) c.2145C>G (p.Pro715=) | gnomAD v4 |
9 | g.91724340G= | CA1863922657 | ROR2 | c.2154C= (p.Pro718=) c.1734C= (p.Pro578=) n.2622C= c.951C= (p.Pro317=) c.2145C= (p.Pro715=) | |
9 | g.91724340G>T | CA466338940 | ROR2 | c.2154C>A (p.Pro718=) c.1734C>A (p.Pro578=) n.2622C>A c.951C>A (p.Pro317=) c.2145C>A (p.Pro715=) | |
9 | g.91724341G>A | CA373795752 | ROR2 | c.2153C>T (p.Pro718Leu) c.1733C>T (p.Pro578Leu) n.2621C>T c.950C>T (p.Pro317Leu) c.2144C>T (p.Pro715Leu) | COSMIC |
9 | g.91724341G>C | CA373795754 | ROR2 | c.2153C>G (p.Pro718Arg) c.1733C>G (p.Pro578Arg) n.2621C>G c.950C>G (p.Pro317Arg) c.2144C>G (p.Pro715Arg) | |
9 | g.91724341G>T | CA373795756 | ROR2 | c.2153C>A (p.Pro718His) c.1733C>A (p.Pro578His) n.2621C>A c.950C>A (p.Pro317His) c.2144C>A (p.Pro715His) | |
9 | g.91724342G>A | CA5120473 | ROR2 | c.2152C>T (p.Pro718Ser) c.1732C>T (p.Pro578Ser) n.2620C>T c.949C>T (p.Pro317Ser) c.2143C>T (p.Pro715Ser) | dbSNP ExAC gnomAD v2 gnomAD v4 |
9 | g.91724342G>C | CA373795760 | ROR2 | c.2152C>G (p.Pro718Ala) c.1732C>G (p.Pro578Ala) n.2620C>G c.949C>G (p.Pro317Ala) c.2143C>G (p.Pro715Ala) | |
9 | g.91724342G= | CA1863922663 | ROR2 | c.2152C= (p.Pro718=) c.1732C= (p.Pro578=) n.2620C= c.949C= (p.Pro317=) c.2143C= (p.Pro715=) | |
9 | g.91724342G>T | CA373795762 | ROR2 | c.2152C>A (p.Pro718Thr) c.1732C>A (p.Pro578Thr) n.2620C>A c.949C>A (p.Pro317Thr) c.2143C>A (p.Pro715Thr) | |
9 | g.91724343A= | CA1863922671 | ROR2 | c.2151T= (p.Cys717=) c.1731T= (p.Cys577=) n.2619T= c.948T= (p.Cys316=) c.2142T= (p.Cys714=) | |
9 | g.91724343A>C | CA373795772 | ROR2 | c.2151T>G (p.Cys717Trp) c.1731T>G (p.Cys577Trp) n.2619T>G c.948T>G (p.Cys316Trp) c.2142T>G (p.Cys714Trp) | |
9 | g.91724343A>G | CA5120474 | ROR2 | c.2151T>C (p.Cys717=) c.1731T>C (p.Cys577=) n.2619T>C c.948T>C (p.Cys316=) c.2142T>C (p.Cys714=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
9 | g.91724343A>T | CA373795777 | ROR2 | c.2151T>A (p.Cys717Ter) c.1731T>A (p.Cys577Ter) n.2619T>A c.948T>A (p.Cys316Ter) c.2142T>A (p.Cys714Ter) | |
9 | g.91724345_91724366dup | CA10604225 | ROR2 | c.2130_2151dup (p.Pro718AlafsTer6) c.1710_1731dup (p.Pro578AlafsTer6) n.2598_2619dup c.927_948dup (p.Pro317AlafsTer6) c.2121_2142dup (p.Pro715AlafsTer6) | ClinVar dbSNP |
9 | g.91724344C>A | CA373795781 | ROR2 | c.2150G>T (p.Cys717Phe) c.1730G>T (p.Cys577Phe) n.2618G>T c.947G>T (p.Cys316Phe) c.2141G>T (p.Cys714Phe) | |
9 | g.91724344C= | CA1863922674 | ROR2 | c.2150G= (p.Cys717=) c.1730G= (p.Cys577=) n.2618G= c.947G= (p.Cys316=) c.2141G= (p.Cys714=) | |
9 | g.91724344C>G | CA5120475 | ROR2 | c.2150G>C (p.Cys717Ser) c.1730G>C (p.Cys577Ser) n.2618G>C c.947G>C (p.Cys316Ser) c.2141G>C (p.Cys714Ser) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.91724344C>T | CA373795782 | ROR2 | c.2150G>A (p.Cys717Tyr) c.1730G>A (p.Cys577Tyr) n.2618G>A c.947G>A (p.Cys316Tyr) c.2141G>A (p.Cys714Tyr) | |
9 | g.91724345A>C | CA373795783 | ROR2 | c.2149T>G (p.Cys717Gly) c.1729T>G (p.Cys577Gly) n.2617T>G c.946T>G (p.Cys316Gly) c.2140T>G (p.Cys714Gly) | |
9 | g.91724345A>G | CA373795785 | ROR2 | c.2149T>C (p.Cys717Arg) c.1729T>C (p.Cys577Arg) n.2617T>C c.946T>C (p.Cys316Arg) c.2140T>C (p.Cys714Arg) | gnomAD v4 |
9 | g.91724345A>T | CA373795786 | ROR2 | c.2149T>A (p.Cys717Ser) c.1729T>A (p.Cys577Ser) n.2617T>A c.946T>A (p.Cys316Ser) c.2140T>A (p.Cys714Ser) | |
9 | g.91724346G>A | CA466338943 | ROR2 | c.2148C>T (p.Asp716=) c.1728C>T (p.Asp576=) n.2616C>T c.945C>T (p.Asp315=) c.2139C>T (p.Asp713=) | |
9 | g.91724346G>C | CA373795790 | ROR2 | c.2148C>G (p.Asp716Glu) c.1728C>G (p.Asp576Glu) n.2616C>G c.945C>G (p.Asp315Glu) c.2139C>G (p.Asp713Glu) | |
9 | g.91724346G>T | CA373795798 | ROR2 | c.2148C>A (p.Asp716Glu) c.1728C>A (p.Asp576Glu) n.2616C>A c.945C>A (p.Asp315Glu) c.2139C>A (p.Asp713Glu) | gnomAD v4 |
9 | g.91724347T>A | CA373795800 | ROR2 | c.2147A>T (p.Asp716Val) c.1727A>T (p.Asp576Val) n.2615A>T c.944A>T (p.Asp315Val) c.2138A>T (p.Asp713Val) | |
9 | g.91724347T>C | CA373795802 | ROR2 | c.2147A>G (p.Asp716Gly) c.1727A>G (p.Asp576Gly) n.2615A>G c.944A>G (p.Asp315Gly) c.2138A>G (p.Asp713Gly) | |
9 | g.91724347T>G | CA373795811 | ROR2 | c.2147A>C (p.Asp716Ala) c.1727A>C (p.Asp576Ala) n.2615A>C c.944A>C (p.Asp315Ala) c.2138A>C (p.Asp713Ala) | |
9 | g.91724348C>A | CA373795819 | ROR2 | c.2146G>T (p.Asp716Tyr) c.1726G>T (p.Asp576Tyr) n.2614G>T c.943G>T (p.Asp315Tyr) c.2137G>T (p.Asp713Tyr) | |
9 | g.91724348C>G | CA373795820 | ROR2 | c.2146G>C (p.Asp716His) c.1726G>C (p.Asp576His) n.2614G>C c.943G>C (p.Asp315His) c.2137G>C (p.Asp713His) | |
9 | g.91724348C>T | CA373795818 | ROR2 | c.2146G>A (p.Asp716Asn) c.1726G>A (p.Asp576Asn) n.2614G>A c.943G>A (p.Asp315Asn) c.2137G>A (p.Asp713Asn) | |
9 | g.91724349A= | CA1863922679 | ROR2 | c.2145T= (p.Asp715=) c.1725T= (p.Asp575=) n.2613T= c.942T= (p.Asp314=) c.2136T= (p.Asp712=) | |
9 | g.91724349A>C | CA373795821 | ROR2 | c.2145T>G (p.Asp715Glu) c.1725T>G (p.Asp575Glu) n.2613T>G c.942T>G (p.Asp314Glu) c.2136T>G (p.Asp712Glu) | |
9 | g.91724349A>G | CA466338946 | ROR2 | c.2145T>C (p.Asp715=) c.1725T>C (p.Asp575=) n.2613T>C c.942T>C (p.Asp314=) c.2136T>C (p.Asp712=) | dbSNP gnomAD v2 gnomAD v4 |
9 | g.91724349A>T | CA373795822 | ROR2 | c.2145T>A (p.Asp715Glu) c.1725T>A (p.Asp575Glu) n.2613T>A c.942T>A (p.Asp314Glu) c.2136T>A (p.Asp712Glu) | |
9 | g.91724350T>A | CA373795823 | ROR2 | c.2144A>T (p.Asp715Val) c.1724A>T (p.Asp575Val) n.2612A>T c.941A>T (p.Asp314Val) c.2135A>T (p.Asp712Val) | |
9 | g.91724350T>C | CA373795824 | ROR2 | c.2144A>G (p.Asp715Gly) c.1724A>G (p.Asp575Gly) n.2612A>G c.941A>G (p.Asp314Gly) c.2135A>G (p.Asp712Gly) | dbSNP gnomAD v2 gnomAD v4 |
9 | g.91724350T>G | CA373795827 | ROR2 | c.2144A>C (p.Asp715Ala) c.1724A>C (p.Asp575Ala) n.2612A>C c.941A>C (p.Asp314Ala) c.2135A>C (p.Asp712Ala) | |
9 | g.91724350T= | CA1863922682 | ROR2 | c.2144A= (p.Asp715=) c.1724A= (p.Asp575=) n.2612A= c.941A= (p.Asp314=) c.2135A= (p.Asp712=) | |
9 | g.91724351C>A | CA373795829 | ROR2 | c.2143G>T (p.Asp715Tyr) c.1723G>T (p.Asp575Tyr) n.2611G>T c.940G>T (p.Asp314Tyr) c.2134G>T (p.Asp712Tyr) | |
9 | g.91724351C= | CA1863922685 | ROR2 | c.2143G= (p.Asp715=) c.1723G= (p.Asp575=) n.2611G= c.940G= (p.Asp314=) c.2134G= (p.Asp712=) | |
9 | g.91724351C>G | CA373795831 | ROR2 | c.2143G>C (p.Asp715His) c.1723G>C (p.Asp575His) n.2611G>C c.940G>C (p.Asp314His) c.2134G>C (p.Asp712His) | dbSNP gnomAD v4 |
9 | g.91724351C>T | CA5120476 | ROR2 | c.2143G>A (p.Asp715Asn) c.1723G>A (p.Asp575Asn) n.2611G>A c.940G>A (p.Asp314Asn) c.2134G>A (p.Asp712Asn) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.91724352G>A | CA5120477 | ROR2 | c.2142C>T (p.Pro714=) c.1722C>T (p.Pro574=) n.2610C>T c.939C>T (p.Pro313=) c.2133C>T (p.Pro711=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
9 | g.91724352G>C | CA5120478 | ROR2 | c.2142C>G (p.Pro714=) c.1722C>G (p.Pro574=) n.2610C>G c.939C>G (p.Pro313=) c.2133C>G (p.Pro711=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
9 | g.91724352G= | CA1863922689 | ROR2 | c.2142C= (p.Pro714=) c.1722C= (p.Pro574=) n.2610C= c.939C= (p.Pro313=) c.2133C= (p.Pro711=) | |
9 | g.91724352G>T | CA466338948 | ROR2 | c.2142C>A (p.Pro714=) c.1722C>A (p.Pro574=) n.2610C>A c.939C>A (p.Pro313=) c.2133C>A (p.Pro711=) | gnomAD v4 |
9 | g.91724353G>A | CA373795852 | ROR2 | c.2141C>T (p.Pro714Leu) c.1721C>T (p.Pro574Leu) n.2609C>T c.938C>T (p.Pro313Leu) c.2132C>T (p.Pro711Leu) | |
9 | g.91724353G>C | CA373795858 | ROR2 | c.2141C>G (p.Pro714Arg) c.1721C>G (p.Pro574Arg) n.2609C>G c.938C>G (p.Pro313Arg) c.2132C>G (p.Pro711Arg) | |
9 | g.91724353G>T | CA373795859 | ROR2 | c.2141C>A (p.Pro714His) c.1721C>A (p.Pro574His) n.2609C>A c.938C>A (p.Pro313His) c.2132C>A (p.Pro711His) | gnomAD v4 |
9 | g.91724354G>A | CA373795868 | ROR2 | c.2140C>T (p.Pro714Ser) c.1720C>T (p.Pro574Ser) n.2608C>T c.937C>T (p.Pro313Ser) c.2131C>T (p.Pro711Ser) | |
9 | g.91724354G>C | CA373795871 | ROR2 | c.2140C>G (p.Pro714Ala) c.1720C>G (p.Pro574Ala) n.2608C>G c.937C>G (p.Pro313Ala) c.2131C>G (p.Pro711Ala) | |
9 | g.91724354G>T | CA373795864 | ROR2 | c.2140C>A (p.Pro714Thr) c.1720C>A (p.Pro574Thr) n.2608C>A c.937C>A (p.Pro313Thr) c.2131C>A (p.Pro711Thr) | |
9 | g.91724355G>A | CA466338949 | ROR2 | c.2139C>T (p.Cys713=) c.1719C>T (p.Cys573=) n.2607C>T c.936C>T (p.Cys312=) c.2130C>T (p.Cys710=) | dbSNP gnomAD v3 gnomAD v4 |
9 | g.91724355G>C | CA373795875 | ROR2 | c.2139C>G (p.Cys713Trp) c.1719C>G (p.Cys573Trp) n.2607C>G c.936C>G (p.Cys312Trp) c.2130C>G (p.Cys710Trp) | |
9 | g.91724355G= | CA1863922695 | ROR2 | c.2139C= (p.Cys713=) c.1719C= (p.Cys573=) n.2607C= c.936C= (p.Cys312=) c.2130C= (p.Cys710=) | |
9 | g.91724355G>T | CA373795877 | ROR2 | c.2139C>A (p.Cys713Ter) c.1719C>A (p.Cys573Ter) n.2607C>A c.936C>A (p.Cys312Ter) c.2130C>A (p.Cys710Ter) | |
9 | g.91724356C>A | CA373795879 | ROR2 | c.2138G>T (p.Cys713Phe) c.1718G>T (p.Cys573Phe) n.2606G>T c.935G>T (p.Cys312Phe) c.2129G>T (p.Cys710Phe) | |
9 | g.91724356C= | CA1863922699 | ROR2 | c.2138G= (p.Cys713=) c.1718G= (p.Cys573=) n.2606G= c.935G= (p.Cys312=) c.2129G= (p.Cys710=) | |
9 | g.91724356C>G | CA373795880 | ROR2 | c.2138G>C (p.Cys713Ser) c.1718G>C (p.Cys573Ser) n.2606G>C c.935G>C (p.Cys312Ser) c.2129G>C (p.Cys710Ser) | |
9 | g.91724356C>T | CA5120479 | ROR2 | c.2138G>A (p.Cys713Tyr) c.1718G>A (p.Cys573Tyr) n.2606G>A c.935G>A (p.Cys312Tyr) c.2129G>A (p.Cys710Tyr) | dbSNP ExAC gnomAD v2 gnomAD v4 |
9 | g.91724357A>C | CA373795885 | ROR2 | c.2137T>G (p.Cys713Gly) c.1717T>G (p.Cys573Gly) n.2605T>G c.934T>G (p.Cys312Gly) c.2128T>G (p.Cys710Gly) | |
9 | g.91724357A>G | CA373795882 | ROR2 | c.2137T>C (p.Cys713Arg) c.1717T>C (p.Cys573Arg) n.2605T>C c.934T>C (p.Cys312Arg) c.2128T>C (p.Cys710Arg) | |
9 | g.91724357A>T | CA373795881 | ROR2 | c.2137T>A (p.Cys713Ser) c.1717T>A (p.Cys573Ser) n.2605T>A c.934T>A (p.Cys312Ser) c.2128T>A (p.Cys710Ser) | |
9 | g.91724358A>C | CA466338955 | ROR2 | c.2136T>G (p.Pro712=) c.1716T>G (p.Pro572=) n.2604T>G c.933T>G (p.Pro311=) c.2127T>G (p.Pro709=) | gnomAD v4 |
9 | g.91724358A>G | CA466338954 | ROR2 | c.2136T>C (p.Pro712=) c.1716T>C (p.Pro572=) n.2604T>C c.933T>C (p.Pro311=) c.2127T>C (p.Pro709=) | |
9 | g.91724358A>T | CA466338953 | ROR2 | c.2136T>A (p.Pro712=) c.1716T>A (p.Pro572=) n.2604T>A c.933T>A (p.Pro311=) c.2127T>A (p.Pro709=) | |
9 | g.91724359G>A | CA373795887 | ROR2 | c.2135C>T (p.Pro712Leu) c.1715C>T (p.Pro572Leu) n.2603C>T c.932C>T (p.Pro311Leu) c.2126C>T (p.Pro709Leu) | ClinVar gnomAD v4 |
9 | g.91724359G>C | CA373795888 | ROR2 | c.2135C>G (p.Pro712Arg) c.1715C>G (p.Pro572Arg) n.2603C>G c.932C>G (p.Pro311Arg) c.2126C>G (p.Pro709Arg) | gnomAD v4 |
9 | g.91724359G>T | CA373795889 | ROR2 | c.2135C>A (p.Pro712His) c.1715C>A (p.Pro572His) n.2603C>A c.932C>A (p.Pro311His) c.2126C>A (p.Pro709His) | |
9 | g.91724360G>A | CA5120480 | ROR2 | c.2134C>T (p.Pro712Ser) c.1714C>T (p.Pro572Ser) n.2602C>T c.931C>T (p.Pro311Ser) c.2125C>T (p.Pro709Ser) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
9 | g.91724360G>C | CA373795892 | ROR2 | c.2134C>G (p.Pro712Ala) c.1714C>G (p.Pro572Ala) n.2602C>G c.931C>G (p.Pro311Ala) c.2125C>G (p.Pro709Ala) | |
9 | g.91724360G= | CA1863922701 | ROR2 | c.2134C= (p.Pro712=) c.1714C= (p.Pro572=) n.2602C= c.931C= (p.Pro311=) c.2125C= (p.Pro709=) | |
9 | g.91724360G>T | CA373795894 | ROR2 | c.2134C>A (p.Pro712Thr) c.1714C>A (p.Pro572Thr) n.2602C>A c.931C>A (p.Pro311Thr) c.2125C>A (p.Pro709Thr) | |
9 | g.91724361C>A | CA466338960 | ROR2 | c.2133G>T (p.Leu711=) c.1713G>T (p.Leu571=) n.2601G>T c.930G>T (p.Leu310=) c.2124G>T (p.Leu708=) | |
9 | g.91724361C= | CA1863922703 | ROR2 | c.2133G= (p.Leu711=) c.1713G= (p.Leu571=) n.2601G= c.930G= (p.Leu310=) c.2124G= (p.Leu708=) | |
9 | g.91724361C>G | CA466338959 | ROR2 | c.2133G>C (p.Leu711=) c.1713G>C (p.Leu571=) n.2601G>C c.930G>C (p.Leu310=) c.2124G>C (p.Leu708=) | |
9 | g.91724361C>T | CA466338958 | ROR2 | c.2133G>A (p.Leu711=) c.1713G>A (p.Leu571=) n.2601G>A c.930G>A (p.Leu310=) c.2124G>A (p.Leu708=) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
9 | g.91724362A= | CA1863922707 | ROR2 | c.2132T= (p.Leu711=) c.1712T= (p.Leu571=) n.2600T= c.929T= (p.Leu310=) c.2123T= (p.Leu708=) | |
9 | g.91724362A>C | CA373795912 | ROR2 | c.2132T>G (p.Leu711Arg) c.1712T>G (p.Leu571Arg) n.2600T>G c.929T>G (p.Leu310Arg) c.2123T>G (p.Leu708Arg) | |
9 | g.91724362A>G | CA373795908 | ROR2 | c.2132T>C (p.Leu711Pro) c.1712T>C (p.Leu571Pro) n.2600T>C c.929T>C (p.Leu310Pro) c.2123T>C (p.Leu708Pro) | |
9 | g.91724362A>T | CA373795904 | ROR2 | c.2132T>A (p.Leu711Gln) c.1712T>A (p.Leu571Gln) n.2600T>A c.929T>A (p.Leu310Gln) c.2123T>A (p.Leu708Gln) | dbSNP |
9 | g.91724363G>A | CA466338961 | ROR2 | c.2131C>T (p.Leu711=) c.1711C>T (p.Leu571=) n.2599C>T c.928C>T (p.Leu310=) c.2122C>T (p.Leu708=) | |
9 | g.91724363G>C | CA373795913 | ROR2 | c.2131C>G (p.Leu711Val) c.1711C>G (p.Leu571Val) n.2599C>G c.928C>G (p.Leu310Val) c.2122C>G (p.Leu708Val) | |
9 | g.91724363G>T | CA373795915 | ROR2 | c.2131C>A (p.Leu711Met) c.1711C>A (p.Leu571Met) n.2599C>A c.928C>A (p.Leu310Met) c.2122C>A (p.Leu708Met) | gnomAD v4 |
9 | g.91724364C>A | CA466338962 | ROR2 | c.2130G>T (p.Val710=) c.1710G>T (p.Val570=) n.2598G>T c.927G>T (p.Val309=) c.2121G>T (p.Val707=) | |
9 | g.91724364C>G | CA466338964 | ROR2 | c.2130G>C (p.Val710=) c.1710G>C (p.Val570=) n.2598G>C c.927G>C (p.Val309=) c.2121G>C (p.Val707=) | |
9 | g.91724364C>T | CA466338963 | ROR2 | c.2130G>A (p.Val710=) c.1710G>A (p.Val570=) n.2598G>A c.927G>A (p.Val309=) c.2121G>A (p.Val707=) | |
9 | g.91724365A= | CA1863922708 | ROR2 | c.2129T= (p.Val710=) c.1709T= (p.Val570=) n.2597T= c.926T= (p.Val309=) c.2120T= (p.Val707=) | |
9 | g.91724365A>C | CA5120481 | ROR2 | c.2129T>G (p.Val710Gly) c.1709T>G (p.Val570Gly) n.2597T>G c.926T>G (p.Val309Gly) c.2120T>G (p.Val707Gly) | dbSNP ExAC gnomAD v2 gnomAD v4 |
9 | g.91724365A>G | CA5120482 | ROR2 | c.2129T>C (p.Val710Ala) c.1709T>C (p.Val570Ala) n.2597T>C c.926T>C (p.Val309Ala) c.2120T>C (p.Val707Ala) | dbSNP ExAC gnomAD v2 gnomAD v4 |
9 | g.91724365A>T | CA373795927 | ROR2 | c.2129T>A (p.Val710Glu) c.1709T>A (p.Val570Glu) n.2597T>A c.926T>A (p.Val309Glu) c.2120T>A (p.Val707Glu) | |
9 | g.91724366C>A | CA373795929 | ROR2 | c.2128G>T (p.Val710Leu) c.1708G>T (p.Val570Leu) n.2596G>T c.925G>T (p.Val309Leu) c.2119G>T (p.Val707Leu) | |
9 | g.91724366C= | CA1863922712 | ROR2 | c.2128G= (p.Val710=) c.1708G= (p.Val570=) n.2596G= c.925G= (p.Val309=) c.2119G= (p.Val707=) | |
9 | g.91724366C>G | CA373795932 | ROR2 | c.2128G>C (p.Val710Leu) c.1708G>C (p.Val570Leu) n.2596G>C c.925G>C (p.Val309Leu) c.2119G>C (p.Val707Leu) | |
9 | g.91724366C>T | CA373795935 | ROR2 | c.2128G>A (p.Val710Met) c.1708G>A (p.Val570Met) n.2596G>A c.925G>A (p.Val309Met) c.2119G>A (p.Val707Met) | dbSNP gnomAD v3 gnomAD v4 |
9 | g.91724367C>A | CA373795939 | ROR2 | c.2127G>T (p.Gln709His) c.1707G>T (p.Gln569His) n.2595G>T c.924G>T (p.Gln308His) c.2118G>T (p.Gln706His) | |
9 | g.91724367C>G | CA373795943 | ROR2 | c.2127G>C (p.Gln709His) c.1707G>C (p.Gln569His) n.2595G>C c.924G>C (p.Gln308His) c.2118G>C (p.Gln706His) | |
9 | g.91724367C>T | CA466338966 | ROR2 | c.2127G>A (p.Gln709=) c.1707G>A (p.Gln569=) n.2595G>A c.924G>A (p.Gln308=) c.2118G>A (p.Gln706=) | |
9 | g.91724368T>A | CA373795946 | ROR2 | c.2126A>T (p.Gln709Leu) c.1706A>T (p.Gln569Leu) n.2594A>T c.923A>T (p.Gln308Leu) c.2117A>T (p.Gln706Leu) | |
9 | g.91724368T>C | CA373795950 | ROR2 | c.2126A>G (p.Gln709Arg) c.1706A>G (p.Gln569Arg) n.2594A>G c.923A>G (p.Gln308Arg) c.2117A>G (p.Gln706Arg) | |
9 | g.91724368T>G | CA373795952 | ROR2 | c.2126A>C (p.Gln709Pro) c.1706A>C (p.Gln569Pro) n.2594A>C c.923A>C (p.Gln308Pro) c.2117A>C (p.Gln706Pro) | |
9 | g.91724369G>A | CA373795962 | ROR2 | c.2125C>T (p.Gln709Ter) c.1705C>T (p.Gln569Ter) n.2593C>T c.922C>T (p.Gln308Ter) c.2116C>T (p.Gln706Ter) | |
9 | g.91724369G>C | CA373795958 | ROR2 | c.2125C>G (p.Gln709Glu) c.1705C>G (p.Gln569Glu) n.2593C>G c.922C>G (p.Gln308Glu) c.2116C>G (p.Gln706Glu) | |
9 | g.91724369G>T | CA373795955 | ROR2 | c.2125C>A (p.Gln709Lys) c.1705C>A (p.Gln569Lys) n.2593C>A c.922C>A (p.Gln308Lys) c.2116C>A (p.Gln706Lys) | |
9 | g.91724370C>A | CA466338969 | ROR2 | c.2124G>T (p.Arg708=) c.1704G>T (p.Arg568=) n.2592G>T c.921G>T (p.Arg307=) c.2115G>T (p.Arg705=) | gnomAD v4 |
9 | g.91724370C>G | CA466338970 | ROR2 | c.2124G>C (p.Arg708=) c.1704G>C (p.Arg568=) n.2592G>C c.921G>C (p.Arg307=) c.2115G>C (p.Arg705=) | |
9 | g.91724370C>T | CA466338971 | ROR2 | c.2124G>A (p.Arg708=) c.1704G>A (p.Arg568=) n.2592G>A c.921G>A (p.Arg307=) c.2115G>A (p.Arg705=) | COSMIC |
9 | g.91724371C>A | CA373795965 | ROR2 | c.2123G>T (p.Arg708Leu) c.1703G>T (p.Arg568Leu) n.2591G>T c.920G>T (p.Arg307Leu) c.2114G>T (p.Arg705Leu) | |
9 | g.91724371C= | CA1863922715 | ROR2 | c.2123G= (p.Arg708=) c.1703G= (p.Arg568=) n.2591G= c.920G= (p.Arg307=) c.2114G= (p.Arg705=) | |
9 | g.91724371C>G | CA373795973 | ROR2 | c.2123G>C (p.Arg708Pro) c.1703G>C (p.Arg568Pro) n.2591G>C c.920G>C (p.Arg307Pro) c.2114G>C (p.Arg705Pro) | gnomAD v4 |
9 | g.91724371C>T | CA5120483 | ROR2 | c.2123G>A (p.Arg708Gln) c.1703G>A (p.Arg568Gln) n.2591G>A c.920G>A (p.Arg307Gln) c.2114G>A (p.Arg705Gln) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.91724372G>A | CA5120484 | ROR2 | c.2122C>T (p.Arg708Trp) c.1702C>T (p.Arg568Trp) n.2590C>T c.919C>T (p.Arg307Trp) c.2113C>T (p.Arg705Trp) | dbSNP ExAC gnomAD v2 gnomAD v4 |
9 | g.91724372G>C | CA373795974 | ROR2 | c.2122C>G (p.Arg708Gly) c.1702C>G (p.Arg568Gly) n.2590C>G c.919C>G (p.Arg307Gly) c.2113C>G (p.Arg705Gly) | |
9 | g.91724372G= | CA1863922718 | ROR2 | c.2122C= (p.Arg708=) c.1702C= (p.Arg568=) n.2590C= c.919C= (p.Arg307=) c.2113C= (p.Arg705=) | |
9 | g.91724372G>T | CA466338973 | ROR2 | c.2122C>A (p.Arg708=) c.1702C>A (p.Arg568=) n.2590C>A c.919C>A (p.Arg307=) c.2113C>A (p.Arg705=) | COSMIC |
9 | g.91724373G>A | CA466338974 | ROR2 | c.2121C>T (p.Asn707=) c.1701C>T (p.Asn567=) n.2589C>T c.918C>T (p.Asn306=) c.2112C>T (p.Asn704=) | |
9 | g.91724373G>C | CA373795978 | ROR2 | c.2121C>G (p.Asn707Lys) c.1701C>G (p.Asn567Lys) n.2589C>G c.918C>G (p.Asn306Lys) c.2112C>G (p.Asn704Lys) | |
9 | g.91724373G= | CA1863922719 | ROR2 | c.2121C= (p.Asn707=) c.1701C= (p.Asn567=) n.2589C= c.918C= (p.Asn306=) c.2112C= (p.Asn704=) | |
9 | g.91724373G>T | CA373795979 | ROR2 | c.2121C>A (p.Asn707Lys) c.1701C>A (p.Asn567Lys) n.2589C>A c.918C>A (p.Asn306Lys) c.2112C>A (p.Asn704Lys) | dbSNP gnomAD v4 |
9 | g.91724374T>A | CA373795983 | ROR2 | c.2120A>T (p.Asn707Ile) c.1700A>T (p.Asn567Ile) n.2588A>T c.917A>T (p.Asn306Ile) c.2111A>T (p.Asn704Ile) | |
9 | g.91724374T>C | CA373795986 | ROR2 | c.2120A>G (p.Asn707Ser) c.1700A>G (p.Asn567Ser) n.2588A>G c.917A>G (p.Asn306Ser) c.2111A>G (p.Asn704Ser) | |
9 | g.91724374T>G | CA373795995 | ROR2 | c.2120A>C (p.Asn707Thr) c.1700A>C (p.Asn567Thr) n.2588A>C c.917A>C (p.Asn306Thr) c.2111A>C (p.Asn704Thr) | dbSNP |
9 | g.91724374T= | CA1863922720 | ROR2 | c.2120A= (p.Asn707=) c.1700A= (p.Asn567=) n.2588A= c.917A= (p.Asn306=) c.2111A= (p.Asn704=) | |
9 | g.91724375T>A | CA373795996 | ROR2 | c.2119A>T (p.Asn707Tyr) c.1699A>T (p.Asn567Tyr) n.2587A>T c.916A>T (p.Asn306Tyr) c.2110A>T (p.Asn704Tyr) | |
9 | g.91724375T>C | CA373795997 | ROR2 | c.2119A>G (p.Asn707Asp) c.1699A>G (p.Asn567Asp) n.2587A>G c.916A>G (p.Asn306Asp) c.2110A>G (p.Asn704Asp) | |
9 | g.91724375T>G | CA373795998 | ROR2 | c.2119A>C (p.Asn707His) c.1699A>C (p.Asn567His) n.2587A>C c.916A>C (p.Asn306His) c.2110A>C (p.Asn704His) | |
9 | g.91724376C>A | CA466338978 | ROR2 | c.2118G>T (p.Arg706=) c.1698G>T (p.Arg566=) n.2586G>T c.915G>T (p.Arg305=) c.2109G>T (p.Arg703=) | |
9 | g.91724376C>G | CA466338979 | ROR2 | c.2118G>C (p.Arg706=) c.1698G>C (p.Arg566=) n.2586G>C c.915G>C (p.Arg305=) c.2109G>C (p.Arg703=) | |
9 | g.91724376C>T | CA466338980 | ROR2 | c.2118G>A (p.Arg706=) c.1698G>A (p.Arg566=) n.2586G>A c.915G>A (p.Arg305=) c.2109G>A (p.Arg703=) | |
9 | g.91724377C>A | CA373796000 | ROR2 | c.2117G>T (p.Arg706Leu) c.1697G>T (p.Arg566Leu) n.2585G>T c.914G>T (p.Arg305Leu) c.2108G>T (p.Arg703Leu) | |
9 | g.91724377C= | CA1863922721 | ROR2 | c.2117G= (p.Arg706=) c.1697G= (p.Arg566=) n.2585G= c.914G= (p.Arg305=) c.2108G= (p.Arg703=) | |
9 | g.91724377C>G | CA373795999 | ROR2 | c.2117G>C (p.Arg706Pro) c.1697G>C (p.Arg566Pro) n.2585G>C c.914G>C (p.Arg305Pro) c.2108G>C (p.Arg703Pro) | |
9 | g.91724377C>T | CA5120485 | ROR2 | c.2117G>A (p.Arg706Gln) c.1697G>A (p.Arg566Gln) n.2585G>A c.914G>A (p.Arg305Gln) c.2108G>A (p.Arg703Gln) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
9 | g.91724378G>A | CA5120486 | ROR2 | c.2116C>T (p.Arg706Trp) c.1696C>T (p.Arg566Trp) n.2584C>T c.913C>T (p.Arg305Trp) c.2107C>T (p.Arg703Trp) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.91724378G>C | CA373796002 | ROR2 | c.2116C>G (p.Arg706Gly) c.1696C>G (p.Arg566Gly) n.2584C>G c.913C>G (p.Arg305Gly) c.2107C>G (p.Arg703Gly) | gnomAD v4 |
9 | g.91724378G= | CA1863922722 | ROR2 | c.2116C= (p.Arg706=) c.1696C= (p.Arg566=) n.2584C= c.913C= (p.Arg305=) c.2107C= (p.Arg703=) | |
9 | g.91724378G>T | CA466338982 | ROR2 | c.2116C>A (p.Arg706=) c.1696C>A (p.Arg566=) n.2584C>A c.913C>A (p.Arg305=) c.2107C>A (p.Arg703=) | |
9 | g.91724379G>A | CA466338983 | ROR2 | c.2115C>T (p.Ile705=) c.1695C>T (p.Ile565=) n.2583C>T c.912C>T (p.Ile304=) c.2106C>T (p.Ile702=) | |
9 | g.91724379G>C | CA373796008 | ROR2 | c.2115C>G (p.Ile705Met) c.1695C>G (p.Ile565Met) n.2583C>G c.912C>G (p.Ile304Met) c.2106C>G (p.Ile702Met) | |
9 | g.91724379G>T | CA466338984 | ROR2 | c.2115C>A (p.Ile705=) c.1695C>A (p.Ile565=) n.2583C>A c.912C>A (p.Ile304=) c.2106C>A (p.Ile702=) | |
9 | g.91724380A>C | CA373796011 | ROR2 | c.2114T>G (p.Ile705Ser) c.1694T>G (p.Ile565Ser) n.2582T>G c.911T>G (p.Ile304Ser) c.2105T>G (p.Ile702Ser) | |
9 | g.91724380A>G | CA373796012 | ROR2 | c.2114T>C (p.Ile705Thr) c.1694T>C (p.Ile565Thr) n.2582T>C c.911T>C (p.Ile304Thr) c.2105T>C (p.Ile702Thr) | |
9 | g.91724380A>T | CA373796013 | ROR2 | c.2114T>A (p.Ile705Asn) c.1694T>A (p.Ile565Asn) n.2582T>A c.911T>A (p.Ile304Asn) c.2105T>A (p.Ile702Asn) | |
9 | g.91724381T>A | CA373796025 | ROR2 | c.2113A>T (p.Ile705Phe) c.1693A>T (p.Ile565Phe) n.2581A>T c.910A>T (p.Ile304Phe) c.2104A>T (p.Ile702Phe) | |
9 | g.91724381T>C | CA373796022 | ROR2 | c.2113A>G (p.Ile705Val) c.1693A>G (p.Ile565Val) n.2581A>G c.910A>G (p.Ile304Val) c.2104A>G (p.Ile702Val) | gnomAD v4 |
9 | g.91724381T>G | CA373796020 | ROR2 | c.2113A>C (p.Ile705Leu) c.1693A>C (p.Ile565Leu) n.2581A>C c.910A>C (p.Ile304Leu) c.2104A>C (p.Ile702Leu) | |
9 | g.91724382C>A | CA373796026 | ROR2 | c.2112G>T (p.Met704Ile) c.1692G>T (p.Met564Ile) n.2580G>T c.909G>T (p.Met303Ile) c.2103G>T (p.Met701Ile) | |
9 | g.91724382C= | CA1863922723 | ROR2 | c.2112G= (p.Met704=) c.1692G= (p.Met564=) n.2580G= c.909G= (p.Met303=) c.2103G= (p.Met701=) | |
9 | g.91724382C>G | CA373796027 | ROR2 | c.2112G>C (p.Met704Ile) c.1692G>C (p.Met564Ile) n.2580G>C c.909G>C (p.Met303Ile) c.2103G>C (p.Met701Ile) | |
9 | g.91724382C>T | CA5120487 | ROR2 | c.2112G>A (p.Met704Ile) c.1692G>A (p.Met564Ile) n.2580G>A c.909G>A (p.Met303Ile) c.2103G>A (p.Met701Ile) | dbSNP ExAC gnomAD v2 gnomAD v4 |
9 | g.91724383A>C | CA373796028 | ROR2 | c.2111T>G (p.Met704Arg) c.1691T>G (p.Met564Arg) n.2579T>G c.908T>G (p.Met303Arg) c.2102T>G (p.Met701Arg) | |
9 | g.91724383A>G | CA373796031 | ROR2 | c.2111T>C (p.Met704Thr) c.1691T>C (p.Met564Thr) n.2579T>C c.908T>C (p.Met303Thr) c.2102T>C (p.Met701Thr) | gnomAD v4 |
9 | g.91724383A>T | CA373796033 | ROR2 | c.2111T>A (p.Met704Lys) c.1691T>A (p.Met564Lys) n.2579T>A c.908T>A (p.Met303Lys) c.2102T>A (p.Met701Lys) | |
9 | g.91724384T>A | CA373796036 | ROR2 | c.2110A>T (p.Met704Leu) c.1690A>T (p.Met564Leu) n.2578A>T c.907A>T (p.Met303Leu) c.2101A>T (p.Met701Leu) | |
9 | g.91724384T>C | CA5120488 | ROR2 | c.2110A>G (p.Met704Val) c.1690A>G (p.Met564Val) n.2578A>G c.907A>G (p.Met303Val) c.2101A>G (p.Met701Val) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.91724384T>G | CA373796039 | ROR2 | c.2110A>C (p.Met704Leu) c.1690A>C (p.Met564Leu) n.2578A>C c.907A>C (p.Met303Leu) c.2101A>C (p.Met701Leu) | |
9 | g.91724384T= | CA1863922724 | ROR2 | c.2110A= (p.Met704=) c.1690A= (p.Met564=) n.2578A= c.907A= (p.Met303=) c.2101A= (p.Met701=) | |
9 | g.91724385C>A | CA5120489 | ROR2 | c.2109G>T (p.Glu703Asp) c.1689G>T (p.Glu563Asp) n.2577G>T c.906G>T (p.Glu302Asp) c.2100G>T (p.Glu700Asp) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.91724385C= | CA1863922725 | ROR2 | c.2109G= (p.Glu703=) c.1689G= (p.Glu563=) n.2577G= c.906G= (p.Glu302=) c.2100G= (p.Glu700=) | |
9 | g.91724385C>G | CA373796041 | ROR2 | c.2109G>C (p.Glu703Asp) c.1689G>C (p.Glu563Asp) n.2577G>C c.906G>C (p.Glu302Asp) c.2100G>C (p.Glu700Asp) | |
9 | g.91724385C>T | CA466338989 | ROR2 | c.2109G>A (p.Glu703=) c.1689G>A (p.Glu563=) n.2577G>A c.906G>A (p.Glu302=) c.2100G>A (p.Glu700=) | |
9 | g.91724386T>A | CA373796043 | ROR2 | c.2108A>T (p.Glu703Val) c.1688A>T (p.Glu563Val) n.2576A>T c.905A>T (p.Glu302Val) c.2099A>T (p.Glu700Val) | |
9 | g.91724386T>C | CA373796046 | ROR2 | c.2108A>G (p.Glu703Gly) c.1688A>G (p.Glu563Gly) n.2576A>G c.905A>G (p.Glu302Gly) c.2099A>G (p.Glu700Gly) | gnomAD v4 |
9 | g.91724386T>G | CA373796050 | ROR2 | c.2108A>C (p.Glu703Ala) c.1688A>C (p.Glu563Ala) n.2576A>C c.905A>C (p.Glu302Ala) c.2099A>C (p.Glu700Ala) | |
9 | g.91724387C>A | CA373796051 | ROR2 | c.2107G>T (p.Glu703Ter) c.1687G>T (p.Glu563Ter) n.2575G>T c.904G>T (p.Glu302Ter) c.2098G>T (p.Glu700Ter) | |
9 | g.91724387C>G | CA373796053 | ROR2 | c.2107G>C (p.Glu703Gln) c.1687G>C (p.Glu563Gln) n.2575G>C c.904G>C (p.Glu302Gln) c.2098G>C (p.Glu700Gln) | |
9 | g.91724387C>T | CA373796060 | ROR2 | c.2107G>A (p.Glu703Lys) c.1687G>A (p.Glu563Lys) n.2575G>A c.904G>A (p.Glu302Lys) c.2098G>A (p.Glu700Lys) | ClinVar gnomAD v4 |
9 | g.91724388C>A | CA466338993 | ROR2 | c.2106G>T (p.Val702=) c.1686G>T (p.Val562=) n.2574G>T c.903G>T (p.Val301=) c.2097G>T (p.Val699=) | |
9 | g.91724388C= | CA1863922726 | ROR2 | c.2106G= (p.Val702=) c.1686G= (p.Val562=) n.2574G= c.903G= (p.Val301=) c.2097G= (p.Val699=) | |
9 | g.91724388C>G | CA466338994 | ROR2 | c.2106G>C (p.Val702=) c.1686G>C (p.Val562=) n.2574G>C c.903G>C (p.Val301=) c.2097G>C (p.Val699=) | |
9 | g.91724388C>T | CA5120490 | ROR2 | c.2106G>A (p.Val702=) c.1686G>A (p.Val562=) n.2574G>A c.903G>A (p.Val301=) c.2097G>A (p.Val699=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
9 | g.91724389A>C | CA373796061 | ROR2 | c.2105T>G (p.Val702Gly) c.1685T>G (p.Val562Gly) n.2573T>G c.902T>G (p.Val301Gly) c.2096T>G (p.Val699Gly) | |
9 | g.91724389A>G | CA373796062 | ROR2 | c.2105T>C (p.Val702Ala) c.1685T>C (p.Val562Ala) n.2573T>C c.902T>C (p.Val301Ala) c.2096T>C (p.Val699Ala) | |
9 | g.91724389A>T | CA373796064 | ROR2 | c.2105T>A (p.Val702Glu) c.1685T>A (p.Val562Glu) n.2573T>A c.902T>A (p.Val301Glu) c.2096T>A (p.Val699Glu) | |
9 | g.91724390C>A | CA373796068 | ROR2 | c.2104G>T (p.Val702Leu) c.1684G>T (p.Val562Leu) n.2572G>T c.901G>T (p.Val301Leu) c.2095G>T (p.Val699Leu) | |
9 | g.91724390C>G | CA373796069 | ROR2 | c.2104G>C (p.Val702Leu) c.1684G>C (p.Val562Leu) n.2572G>C c.901G>C (p.Val301Leu) c.2095G>C (p.Val699Leu) | |
9 | g.91724390C>T | CA373796067 | ROR2 | c.2104G>A (p.Val702Met) c.1684G>A (p.Val562Met) n.2572G>A c.901G>A (p.Val301Met) c.2095G>A (p.Val699Met) | |
9 | g.91724391C>A | CA466338995 | ROR2 | c.2103G>T (p.Val701=) c.1683G>T (p.Val561=) n.2571G>T c.900G>T (p.Val300=) c.2094G>T (p.Val698=) | |
9 | g.91724391C>G | CA466338997 | ROR2 | c.2103G>C (p.Val701=) c.1683G>C (p.Val561=) n.2571G>C c.900G>C (p.Val300=) c.2094G>C (p.Val698=) | |
9 | g.91724391C>T | CA466338996 | ROR2 | c.2103G>A (p.Val701=) c.1683G>A (p.Val561=) n.2571G>A c.900G>A (p.Val300=) c.2094G>A (p.Val698=) | |
9 | g.91724392A>C | CA373796070 | ROR2 | c.2102T>G (p.Val701Gly) c.1682T>G (p.Val561Gly) n.2570T>G c.899T>G (p.Val300Gly) c.2093T>G (p.Val698Gly) | |
9 | g.91724392A>G | CA373796071 | ROR2 | c.2102T>C (p.Val701Ala) c.1682T>C (p.Val561Ala) n.2570T>C c.899T>C (p.Val300Ala) c.2093T>C (p.Val698Ala) | |
9 | g.91724392A>T | CA373796072 | ROR2 | c.2102T>A (p.Val701Glu) c.1682T>A (p.Val561Glu) n.2570T>A c.899T>A (p.Val300Glu) c.2093T>A (p.Val698Glu) | |
9 | g.91724393C>A | CA373796073 | ROR2 | c.2101G>T (p.Val701Leu) c.1681G>T (p.Val561Leu) n.2569G>T c.898G>T (p.Val300Leu) c.2092G>T (p.Val698Leu) | gnomAD v4 |
9 | g.91724393C>G | CA373796074 | ROR2 | c.2101G>C (p.Val701Leu) c.1681G>C (p.Val561Leu) n.2569G>C c.898G>C (p.Val300Leu) c.2092G>C (p.Val698Leu) | |
9 | g.91724393C>T | CA373796075 | ROR2 | c.2101G>A (p.Val701Met) c.1681G>A (p.Val561Met) n.2569G>A c.898G>A (p.Val300Met) c.2092G>A (p.Val698Met) | |
9 | g.91724394A>C | CA373796077 | ROR2 | c.2100T>G (p.Asp700Glu) c.1680T>G (p.Asp560Glu) n.2568T>G c.897T>G (p.Asp299Glu) c.2091T>G (p.Asp697Glu) | |
9 | g.91724394A>G | CA466338999 | ROR2 | c.2100T>C (p.Asp700=) c.1680T>C (p.Asp560=) n.2568T>C c.897T>C (p.Asp299=) c.2091T>C (p.Asp697=) | |
9 | g.91724394A>T | CA373796079 | ROR2 | c.2100T>A (p.Asp700Glu) c.1680T>A (p.Asp560Glu) n.2568T>A c.897T>A (p.Asp299Glu) c.2091T>A (p.Asp697Glu) | |
9 | g.91724395T>A | CA373796081 | ROR2 | c.2099A>T (p.Asp700Val) c.1679A>T (p.Asp560Val) n.2567A>T c.896A>T (p.Asp299Val) c.2090A>T (p.Asp697Val) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.91724395T>C | CA5120491 | ROR2 | c.2099A>G (p.Asp700Gly) c.1679A>G (p.Asp560Gly) n.2567A>G c.896A>G (p.Asp299Gly) c.2090A>G (p.Asp697Gly) | dbSNP ExAC gnomAD v2 gnomAD v4 |
9 | g.91724395T>G | CA373796089 | ROR2 | c.2099A>C (p.Asp700Ala) c.1679A>C (p.Asp560Ala) n.2567A>C c.896A>C (p.Asp299Ala) c.2090A>C (p.Asp697Ala) | |
9 | g.91724395T= | CA1863922727 | ROR2 | c.2099A= (p.Asp700=) c.1679A= (p.Asp560=) n.2567A= c.896A= (p.Asp299=) c.2090A= (p.Asp697=) | |
9 | g.91724396C>A | CA373796091 | ROR2 | c.2098G>T (p.Asp700Tyr) c.1678G>T (p.Asp560Tyr) n.2566G>T c.895G>T (p.Asp299Tyr) c.2089G>T (p.Asp697Tyr) | |
9 | g.91724396C= | CA1863922728 | ROR2 | c.2098G= (p.Asp700=) c.1678G= (p.Asp560=) n.2566G= c.895G= (p.Asp299=) c.2089G= (p.Asp697=) | |
9 | g.91724396C>G | CA5120492 | ROR2 | c.2098G>C (p.Asp700His) c.1678G>C (p.Asp560His) n.2566G>C c.895G>C (p.Asp299His) c.2089G>C (p.Asp697His) | dbSNP ExAC gnomAD v2 gnomAD v4 |
9 | g.91724396C>T | CA373796095 | ROR2 | c.2098G>A (p.Asp700Asn) c.1678G>A (p.Asp560Asn) n.2566G>A c.895G>A (p.Asp299Asn) c.2089G>A (p.Asp697Asn) | dbSNP gnomAD v3 gnomAD v4 |
9 | g.91724397del | CA2579378013 | ROR2 | c.2098del (p.Asp700MetfsTer5) c.1678del (p.Asp560MetfsTer5) n.2566del c.895del (p.Asp299MetfsTer5) c.2089del (p.Asp697MetfsTer5) | |
9 | g.91724397C>A | CA373796099 | ROR2 | c.2097G>T (p.Gln699His) c.1677G>T (p.Gln559His) n.2565G>T c.894G>T (p.Gln298His) c.2088G>T (p.Gln696His) | |
9 | g.91724397C>G | CA373796097 | ROR2 | c.2097G>C (p.Gln699His) c.1677G>C (p.Gln559His) n.2565G>C c.894G>C (p.Gln298His) c.2088G>C (p.Gln696His) | |
9 | g.91724397C>T | CA466339003 | ROR2 | c.2097G>A (p.Gln699=) c.1677G>A (p.Gln559=) n.2565G>A c.894G>A (p.Gln298=) c.2088G>A (p.Gln696=) | |
9 | g.91724398T>A | CA373796101 | ROR2 | c.2096A>T (p.Gln699Leu) c.1676A>T (p.Gln559Leu) n.2564A>T c.893A>T (p.Gln298Leu) c.2087A>T (p.Gln696Leu) | |
9 | g.91724398T>C | CA373796105 | ROR2 | c.2096A>G (p.Gln699Arg) c.1676A>G (p.Gln559Arg) n.2564A>G c.893A>G (p.Gln298Arg) c.2087A>G (p.Gln696Arg) | |
9 | g.91724398T>G | CA373796108 | ROR2 | c.2096A>C (p.Gln699Pro) c.1676A>C (p.Gln559Pro) n.2564A>C c.893A>C (p.Gln298Pro) c.2087A>C (p.Gln696Pro) | |
9 | g.91724399G>A | CA373796110 | ROR2 | c.2095C>T (p.Gln699Ter) c.1675C>T (p.Gln559Ter) n.2563C>T c.892C>T (p.Gln298Ter) c.2086C>T (p.Gln696Ter) | |
9 | g.91724399G>C | CA373796113 | ROR2 | c.2095C>G (p.Gln699Glu) c.1675C>G (p.Gln559Glu) n.2563C>G c.892C>G (p.Gln298Glu) c.2086C>G (p.Gln696Glu) | |
9 | g.91724399G>T | CA373796119 | ROR2 | c.2095C>A (p.Gln699Lys) c.1675C>A (p.Gln559Lys) n.2563C>A c.892C>A (p.Gln298Lys) c.2086C>A (p.Gln696Lys) | |
9 | g.91724400G>A | CA466339017 | ROR2 | c.2094C>T (p.Asn698=) c.1674C>T (p.Asn558=) n.2562C>T c.891C>T (p.Asn297=) c.2085C>T (p.Asn695=) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.91724400G>C | CA373796121 | ROR2 | c.2094C>G (p.Asn698Lys) c.1674C>G (p.Asn558Lys) n.2562C>G c.891C>G (p.Asn297Lys) c.2085C>G (p.Asn695Lys) | |
9 | g.91724400G= | CA1863922729 | ROR2 | c.2094C= (p.Asn698=) c.1674C= (p.Asn558=) n.2562C= c.891C= (p.Asn297=) c.2085C= (p.Asn695=) | |
9 | g.91724400G>T | CA373796120 | ROR2 | c.2094C>A (p.Asn698Lys) c.1674C>A (p.Asn558Lys) n.2562C>A c.891C>A (p.Asn297Lys) c.2085C>A (p.Asn695Lys) | |
9 | g.91724401T>A | CA373796122 | ROR2 | c.2093A>T (p.Asn698Ile) c.1673A>T (p.Asn558Ile) n.2561A>T c.890A>T (p.Asn297Ile) c.2084A>T (p.Asn695Ile) | |
9 | g.91724401T>C | CA373796124 | ROR2 | c.2093A>G (p.Asn698Ser) c.1673A>G (p.Asn558Ser) n.2561A>G c.890A>G (p.Asn297Ser) c.2084A>G (p.Asn695Ser) | dbSNP gnomAD v3 gnomAD v4 |
9 | g.91724401T>G | CA373796127 | ROR2 | c.2093A>C (p.Asn698Thr) c.1673A>C (p.Asn558Thr) n.2561A>C c.890A>C (p.Asn297Thr) c.2084A>C (p.Asn695Thr) | |
9 | g.91724401T= | CA1863922730 | ROR2 | c.2093A= (p.Asn698=) c.1673A= (p.Asn558=) n.2561A= c.890A= (p.Asn297=) c.2084A= (p.Asn695=) | |
9 | g.91724402T>A | CA373796131 | ROR2 | c.2092A>T (p.Asn698Tyr) c.1672A>T (p.Asn558Tyr) n.2560A>T c.889A>T (p.Asn297Tyr) c.2083A>T (p.Asn695Tyr) | |
9 | g.91724402T>C | CA373796133 | ROR2 | c.2092A>G (p.Asn698Asp) c.1672A>G (p.Asn558Asp) n.2560A>G c.889A>G (p.Asn297Asp) c.2083A>G (p.Asn695Asp) | gnomAD v4 |
9 | g.91724402T>G | CA373796136 | ROR2 | c.2092A>C (p.Asn698His) c.1672A>C (p.Asn558His) n.2560A>C c.889A>C (p.Asn297His) c.2083A>C (p.Asn695His) | |
9 | g.91724403G>A | CA466339018 | ROR2 | c.2091C>T (p.Ser697=) c.1671C>T (p.Ser557=) n.2559C>T c.888C>T (p.Ser296=) c.2082C>T (p.Ser694=) | dbSNP gnomAD v3 gnomAD v4 COSMIC |
9 | g.91724403G>C | CA466339019 | ROR2 | c.2091C>G (p.Ser697=) c.1671C>G (p.Ser557=) n.2559C>G c.888C>G (p.Ser296=) c.2082C>G (p.Ser694=) | |
9 | g.91724403G= | CA1863922731 | ROR2 | c.2091C= (p.Ser697=) c.1671C= (p.Ser557=) n.2559C= c.888C= (p.Ser296=) c.2082C= (p.Ser694=) | |
9 | g.91724403G>T | CA466339020 | ROR2 | c.2091C>A (p.Ser697=) c.1671C>A (p.Ser557=) n.2559C>A c.888C>A (p.Ser296=) c.2082C>A (p.Ser694=) | |
9 | g.91724404G>A | CA373796138 | ROR2 | c.2090C>T (p.Ser697Phe) c.1670C>T (p.Ser557Phe) n.2558C>T c.887C>T (p.Ser296Phe) c.2081C>T (p.Ser694Phe) | |
9 | g.91724404G>C | CA373796147 | ROR2 | c.2090C>G (p.Ser697Cys) c.1670C>G (p.Ser557Cys) n.2558C>G c.887C>G (p.Ser296Cys) c.2081C>G (p.Ser694Cys) | |
9 | g.91724404G>T | CA373796141 | ROR2 | c.2090C>A (p.Ser697Tyr) c.1670C>A (p.Ser557Tyr) n.2558C>A c.887C>A (p.Ser296Tyr) c.2081C>A (p.Ser694Tyr) | |
9 | g.91724405A= | CA1863922732 | ROR2 | c.2089T= (p.Ser697=) c.1669T= (p.Ser557=) n.2557T= c.886T= (p.Ser296=) c.2080T= (p.Ser694=) | |
9 | g.91724405A>C | CA373796151 | ROR2 | c.2089T>G (p.Ser697Ala) c.1669T>G (p.Ser557Ala) n.2557T>G c.886T>G (p.Ser296Ala) c.2080T>G (p.Ser694Ala) | |
9 | g.91724405A>G | CA5120493 | ROR2 | c.2089T>C (p.Ser697Pro) c.1669T>C (p.Ser557Pro) n.2557T>C c.886T>C (p.Ser296Pro) c.2080T>C (p.Ser694Pro) | dbSNP ExAC gnomAD v2 |
9 | g.91724405A>T | CA373796154 | ROR2 | c.2089T>A (p.Ser697Thr) c.1669T>A (p.Ser557Thr) n.2557T>A c.886T>A (p.Ser296Thr) c.2080T>A (p.Ser694Thr) | |
9 | g.91724406G>A | CA173322 | ROR2 | c.2088C>T (p.Tyr696=) c.1668C>T (p.Tyr556=) n.2556C>T c.885C>T (p.Tyr295=) c.2079C>T (p.Tyr693=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
9 | g.91724406G>C | CA373796157 | ROR2 | c.2088C>G (p.Tyr696Ter) c.1668C>G (p.Tyr556Ter) n.2556C>G c.885C>G (p.Tyr295Ter) c.2079C>G (p.Tyr693Ter) | |
9 | g.91724406G= | CA1863922733 | ROR2 | c.2088C= (p.Tyr696=) c.1668C= (p.Tyr556=) n.2556C= c.885C= (p.Tyr295=) c.2079C= (p.Tyr693=) | |
9 | g.91724406G>T | CA373796160 | ROR2 | c.2088C>A (p.Tyr696Ter) c.1668C>A (p.Tyr556Ter) n.2556C>A c.885C>A (p.Tyr295Ter) c.2079C>A (p.Tyr693Ter) | |
9 | g.91724407T>A | CA373796163 | ROR2 | c.2087A>T (p.Tyr696Phe) c.1667A>T (p.Tyr556Phe) n.2555A>T c.884A>T (p.Tyr295Phe) c.2078A>T (p.Tyr693Phe) | |
9 | g.91724407T>C | CA373796164 | ROR2 | c.2087A>G (p.Tyr696Cys) c.1667A>G (p.Tyr556Cys) n.2555A>G c.884A>G (p.Tyr295Cys) c.2078A>G (p.Tyr693Cys) | dbSNP gnomAD v3 gnomAD v4 |
9 | g.91724407T>G | CA373796167 | ROR2 | c.2087A>C (p.Tyr696Ser) c.1667A>C (p.Tyr556Ser) n.2555A>C c.884A>C (p.Tyr295Ser) c.2078A>C (p.Tyr693Ser) | |
9 | g.91724407T= | CA1863922734 | ROR2 | c.2087A= (p.Tyr696=) c.1667A= (p.Tyr556=) n.2555A= c.884A= (p.Tyr295=) c.2078A= (p.Tyr693=) | |
9 | g.91724408A= | CA1863922736 | ROR2 | c.2086T= (p.Tyr696=) c.1666T= (p.Tyr556=) n.2554T= c.883T= (p.Tyr295=) c.2077T= (p.Tyr693=) | |
9 | g.91724408A>C | CA373796170 | ROR2 | c.2086T>G (p.Tyr696Asp) c.1666T>G (p.Tyr556Asp) n.2554T>G c.883T>G (p.Tyr295Asp) c.2077T>G (p.Tyr693Asp) | |
9 | g.91724408A>G | CA373796173 | ROR2 | c.2086T>C (p.Tyr696His) c.1666T>C (p.Tyr556His) n.2554T>C c.883T>C (p.Tyr295His) c.2077T>C (p.Tyr693His) | dbSNP gnomAD v2 gnomAD v4 |
9 | g.91724408A>T | CA373796176 | ROR2 | c.2086T>A (p.Tyr696Asn) c.1666T>A (p.Tyr556Asn) n.2554T>A c.883T>A (p.Tyr295Asn) c.2077T>A (p.Tyr693Asn) | |
9 | g.91724409C>A | CA5120495 | ROR2 | c.2085G>T (p.Gly695=) c.1665G>T (p.Gly555=) n.2553G>T c.882G>T (p.Gly294=) c.2076G>T (p.Gly692=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
9 | g.91724409C= | CA1863922738 | ROR2 | c.2085G= (p.Gly695=) c.1665G= (p.Gly555=) n.2553G= c.882G= (p.Gly294=) c.2076G= (p.Gly692=) | |
9 | g.91724409C>G | CA466339021 | ROR2 | c.2085G>C (p.Gly695=) c.1665G>C (p.Gly555=) n.2553G>C c.882G>C (p.Gly294=) c.2076G>C (p.Gly692=) | |
9 | g.91724409C>T | CA5120494 | ROR2 | c.2085G>A (p.Gly695=) c.1665G>A (p.Gly555=) n.2553G>A c.882G>A (p.Gly294=) c.2076G>A (p.Gly692=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
9 | g.91724410C>A | CA373796183 | ROR2 | c.2084G>T (p.Gly695Val) c.1664G>T (p.Gly555Val) n.2552G>T c.881G>T (p.Gly294Val) c.2075G>T (p.Gly692Val) | |
9 | g.91724410C= | CA1863922740 | ROR2 | c.2084G= (p.Gly695=) c.1664G= (p.Gly555=) n.2552G= c.881G= (p.Gly294=) c.2075G= (p.Gly692=) | |
9 | g.91724410C>G | CA373796185 | ROR2 | c.2084G>C (p.Gly695Ala) c.1664G>C (p.Gly555Ala) n.2552G>C c.881G>C (p.Gly294Ala) c.2075G>C (p.Gly692Ala) | gnomAD v4 |
9 | g.91724410C>T | CA373796188 | ROR2 | c.2084G>A (p.Gly695Glu) c.1664G>A (p.Gly555Glu) n.2552G>A c.881G>A (p.Gly294Glu) c.2075G>A (p.Gly692Glu) | dbSNP gnomAD v2 gnomAD v4 |
9 | g.91724411C>A | CA373796191 | ROR2 | c.2083G>T (p.Gly695Trp) c.1663G>T (p.Gly555Trp) n.2551G>T c.880G>T (p.Gly294Trp) c.2074G>T (p.Gly692Trp) | |
9 | g.91724411C= | CA1863922741 | ROR2 | c.2083G= (p.Gly695=) c.1663G= (p.Gly555=) n.2551G= c.880G= (p.Gly294=) c.2074G= (p.Gly692=) | |
9 | g.91724411C>G | CA373796192 | ROR2 | c.2083G>C (p.Gly695Arg) c.1663G>C (p.Gly555Arg) n.2551G>C c.880G>C (p.Gly294Arg) c.2074G>C (p.Gly692Arg) | |
9 | g.91724411C>T | CA173320 | ROR2 | c.2083G>A (p.Gly695Arg) c.1663G>A (p.Gly555Arg) n.2551G>A c.880G>A (p.Gly294Arg) c.2074G>A (p.Gly692Arg) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.91724412G>A | CA5120496 | ROR2 | c.2082C>T (p.Cys694=) c.1662C>T (p.Cys554=) n.2550C>T c.879C>T (p.Cys293=) c.2073C>T (p.Cys691=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
9 | g.91724412G>C | CA373796198 | ROR2 | c.2082C>G (p.Cys694Trp) c.1662C>G (p.Cys554Trp) n.2550C>G c.879C>G (p.Cys293Trp) c.2073C>G (p.Cys691Trp) | |
9 | g.91724412G= | CA1863922742 | ROR2 | c.2082C= (p.Cys694=) c.1662C= (p.Cys554=) n.2550C= c.879C= (p.Cys293=) c.2073C= (p.Cys691=) | |
9 | g.91724412G>T | CA373796199 | ROR2 | c.2082C>A (p.Cys694Ter) c.1662C>A (p.Cys554Ter) n.2550C>A c.879C>A (p.Cys293Ter) c.2073C>A (p.Cys691Ter) | |
9 | g.91724413C>A | CA373796201 | ROR2 | c.2081G>T (p.Cys694Phe) c.1661G>T (p.Cys554Phe) n.2549G>T c.878G>T (p.Cys293Phe) c.2072G>T (p.Cys691Phe) | |
9 | g.91724413C>G | CA373796204 | ROR2 | c.2081G>C (p.Cys694Ser) c.1661G>C (p.Cys554Ser) n.2549G>C c.878G>C (p.Cys293Ser) c.2072G>C (p.Cys691Ser) | |
9 | g.91724413C>T | CA373796206 | ROR2 | c.2081G>A (p.Cys694Tyr) c.1661G>A (p.Cys554Tyr) n.2549G>A c.878G>A (p.Cys293Tyr) c.2072G>A (p.Cys691Tyr) | |
9 | g.91724414A= | CA1863922743 | ROR2 | c.2080T= (p.Cys694=) c.1660T= (p.Cys554=) n.2548T= c.877T= (p.Cys293=) c.2071T= (p.Cys691=) | |
9 | g.91724414A>C | CA373796214 | ROR2 | c.2080T>G (p.Cys694Gly) c.1660T>G (p.Cys554Gly) n.2548T>G c.877T>G (p.Cys293Gly) c.2071T>G (p.Cys691Gly) | |
9 | g.91724414A>G | CA248108 | ROR2 | c.2080T>C (p.Cys694Arg) c.1660T>C (p.Cys554Arg) n.2548T>C c.877T>C (p.Cys293Arg) c.2071T>C (p.Cys691Arg) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.91724414A>T | CA373796210 | ROR2 | c.2080T>A (p.Cys694Ser) c.1660T>A (p.Cys554Ser) n.2548T>A c.877T>A (p.Cys293Ser) c.2071T>A (p.Cys691Ser) | |
9 | g.91724415G>A | CA466339022 | ROR2 | c.2079C>T (p.Tyr693=) c.1659C>T (p.Tyr553=) n.2547C>T c.876C>T (p.Tyr292=) c.2070C>T (p.Tyr690=) | |
9 | g.91724415G>C | CA373796216 | ROR2 | c.2079C>G (p.Tyr693Ter) c.1659C>G (p.Tyr553Ter) n.2547C>G c.876C>G (p.Tyr292Ter) c.2070C>G (p.Tyr690Ter) | |
9 | g.91724415G>T | CA373796218 | ROR2 | c.2079C>A (p.Tyr693Ter) c.1659C>A (p.Tyr553Ter) n.2547C>A c.876C>A (p.Tyr292Ter) c.2070C>A (p.Tyr690Ter) | |
9 | g.91724416T>A | CA195322879 | ROR2 | c.2078A>T (p.Tyr693Phe) c.1658A>T (p.Tyr553Phe) n.2546A>T c.875A>T (p.Tyr292Phe) c.2069A>T (p.Tyr690Phe) | dbSNP gnomAD v4 |
9 | g.91724416T>C | CA373796220 | ROR2 | c.2078A>G (p.Tyr693Cys) c.1658A>G (p.Tyr553Cys) n.2546A>G c.875A>G (p.Tyr292Cys) c.2069A>G (p.Tyr690Cys) | gnomAD v4 |
9 | g.91724416T>G | CA373796223 | ROR2 | c.2078A>C (p.Tyr693Ser) c.1658A>C (p.Tyr553Ser) n.2546A>C c.875A>C (p.Tyr292Ser) c.2069A>C (p.Tyr690Ser) | |
9 | g.91724416T= | CA1863922745 | ROR2 | c.2078A= (p.Tyr693=) c.1658A= (p.Tyr553=) n.2546A= c.875A= (p.Tyr292=) c.2069A= (p.Tyr690=) | |
9 | g.91724417A>C | CA373796226 | ROR2 | c.2077T>G (p.Tyr693Asp) c.1657T>G (p.Tyr553Asp) n.2545T>G c.874T>G (p.Tyr292Asp) c.2068T>G (p.Tyr690Asp) | |
9 | g.91724417A>G | CA373796227 | ROR2 | c.2077T>C (p.Tyr693His) c.1657T>C (p.Tyr553His) n.2545T>C c.874T>C (p.Tyr292His) c.2068T>C (p.Tyr690His) | |
9 | g.91724417A>T | CA373796229 | ROR2 | c.2077T>A (p.Tyr693Asn) c.1657T>A (p.Tyr553Asn) n.2545T>A c.874T>A (p.Tyr292Asn) c.2068T>A (p.Tyr690Asn) | |
9 | g.91724418G>A | CA195322884 | ROR2 | c.2076C>T (p.Pro692=) c.1656C>T (p.Pro552=) n.2544C>T c.873C>T (p.Pro291=) c.2067C>T (p.Pro689=) | dbSNP |
9 | g.91724418G>C | CA195322892 | ROR2 | c.2076C>G (p.Pro692=) c.1656C>G (p.Pro552=) n.2544C>G c.873C>G (p.Pro291=) c.2067C>G (p.Pro689=) | ClinVar dbSNP gnomAD v4 |
9 | g.91724418G= | CA1863922749 | ROR2 | c.2076C= (p.Pro692=) c.1656C= (p.Pro552=) n.2544C= c.873C= (p.Pro291=) c.2067C= (p.Pro689=) | |
9 | g.91724418G>T | CA466339023 | ROR2 | c.2076C>A (p.Pro692=) c.1656C>A (p.Pro552=) n.2544C>A c.873C>A (p.Pro291=) c.2067C>A (p.Pro689=) | |
9 | g.91724419G>A | CA373796236 | ROR2 | c.2075C>T (p.Pro692Leu) c.1655C>T (p.Pro552Leu) n.2543C>T c.872C>T (p.Pro291Leu) c.2066C>T (p.Pro689Leu) | dbSNP gnomAD v2 |
9 | g.91724419G>C | CA373796239 | ROR2 | c.2075C>G (p.Pro692Arg) c.1655C>G (p.Pro552Arg) n.2543C>G c.872C>G (p.Pro291Arg) c.2066C>G (p.Pro689Arg) | |
9 | g.91724419G= | CA1863922754 | ROR2 | c.2075C= (p.Pro692=) c.1655C= (p.Pro552=) n.2543C= c.872C= (p.Pro291=) c.2066C= (p.Pro689=) | |
9 | g.91724419G>T | CA373796240 | ROR2 | c.2075C>A (p.Pro692His) c.1655C>A (p.Pro552His) n.2543C>A c.872C>A (p.Pro291His) c.2066C>A (p.Pro689His) | |
9 | g.91724420G>A | CA373796242 | ROR2 | c.2074C>T (p.Pro692Ser) c.1654C>T (p.Pro552Ser) n.2542C>T c.871C>T (p.Pro291Ser) c.2065C>T (p.Pro689Ser) | |
9 | g.91724420G>C | CA373796243 | ROR2 | c.2074C>G (p.Pro692Ala) c.1654C>G (p.Pro552Ala) n.2542C>G c.871C>G (p.Pro291Ala) c.2065C>G (p.Pro689Ala) | |
9 | g.91724420G>T | CA373796245 | ROR2 | c.2074C>A (p.Pro692Thr) c.1654C>A (p.Pro552Thr) n.2542C>A c.871C>A (p.Pro291Thr) c.2065C>A (p.Pro689Thr) | ClinVar dbSNP |
9 | g.91724421C>A | CA373796246 | ROR2 | c.2073G>T (p.Gln691His) c.1653G>T (p.Gln551His) n.2541G>T c.870G>T (p.Gln290His) c.2064G>T (p.Gln688His) | |
9 | g.91724421C>G | CA373796249 | ROR2 | c.2073G>C (p.Gln691His) c.1653G>C (p.Gln551His) n.2541G>C c.870G>C (p.Gln290His) c.2064G>C (p.Gln688His) | |
9 | g.91724421C>T | CA466339024 | ROR2 | c.2073G>A (p.Gln691=) c.1653G>A (p.Gln551=) n.2541G>A c.870G>A (p.Gln290=) c.2064G>A (p.Gln688=) | |
9 | g.91724422T>A | CA373796252 | ROR2 | c.2072A>T (p.Gln691Leu) c.1652A>T (p.Gln551Leu) n.2540A>T c.869A>T (p.Gln290Leu) c.2063A>T (p.Gln688Leu) | |
9 | g.91724422T>C | CA373796254 | ROR2 | c.2072A>G (p.Gln691Arg) c.1652A>G (p.Gln551Arg) n.2540A>G c.869A>G (p.Gln290Arg) c.2063A>G (p.Gln688Arg) | |
9 | g.91724422T>G | CA373796257 | ROR2 | c.2072A>C (p.Gln691Pro) c.1652A>C (p.Gln551Pro) n.2540A>C c.869A>C (p.Gln290Pro) c.2063A>C (p.Gln688Pro) | |
9 | g.91724423G>A | CA373796259 | ROR2 | c.2071C>T (p.Gln691Ter) c.1651C>T (p.Gln551Ter) n.2539C>T c.868C>T (p.Gln290Ter) c.2062C>T (p.Gln688Ter) | dbSNP gnomAD v2 gnomAD v4 |
9 | g.91724423G>C | CA373796261 | ROR2 | c.2071C>G (p.Gln691Glu) c.1651C>G (p.Gln551Glu) n.2539C>G c.868C>G (p.Gln290Glu) c.2062C>G (p.Gln688Glu) | |
9 | g.91724423G= | CA1863922757 | ROR2 | c.2071C= (p.Gln691=) c.1651C= (p.Gln551=) n.2539C= c.868C= (p.Gln290=) c.2062C= (p.Gln688=) | |
9 | g.91724423G>T | CA373796264 | ROR2 | c.2071C>A (p.Gln691Lys) c.1651C>A (p.Gln551Lys) n.2539C>A c.868C>A (p.Gln290Lys) c.2062C>A (p.Gln688Lys) | |
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 |