| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 9 | g.91723935_91723961del | CA2690632285 | ROR2 | c.2540_2566del (p.Ala847_Met855del) c.1920+200_1920+226del (n.1920+200_1920+226del) n.3008_3034del c.2120_2146del (p.Ala707_Met715del) c.1337_1363del (p.Ala446_Met454del) c.2531_2557del (p.Ala844_Met852del) | gnomAD v4 |
| 9 | g.91723938_91723940del | CA5120360 | ROR2 | c.2558_2560del (p.Pro853del) c.1920+218_1920+220del (n.1920+218_1920+220del) n.3026_3028del c.2138_2140del (p.Pro713del) c.1355_1357del (p.Pro452del) c.2549_2551del (p.Pro850del) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 9 | g.91723939G>A | CA373793815 | ROR2 | c.2555C>T (p.Pro852Leu) c.1920+215C>T (n.1920+215C>T) n.3023C>T c.2135C>T (p.Pro712Leu) c.1352C>T (p.Pro451Leu) c.2546C>T (p.Pro849Leu) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 9 | g.91723939G>C | CA373793820 | ROR2 | c.2555C>G (p.Pro852Arg) c.1920+215C>G (n.1920+215C>G) n.3023C>G c.2135C>G (p.Pro712Arg) c.1352C>G (p.Pro451Arg) c.2546C>G (p.Pro849Arg) | |
| 9 | g.91723939G= | CA1863921779 | ROR2 | c.2555C= (p.Pro852=) c.1920+215C= (n.1920+215C=) n.3023C= c.2135C= (p.Pro712=) c.1352C= (p.Pro451=) c.2546C= (p.Pro849=) | |
| 9 | g.91723939G>T | CA373793822 | ROR2 | c.2555C>A (p.Pro852His) c.1920+215C>A (n.1920+215C>A) n.3023C>A c.2135C>A (p.Pro712His) c.1352C>A (p.Pro451His) c.2546C>A (p.Pro849His) | |
| 9 | g.91723940G>A | CA373793828 | ROR2 | c.2554C>T (p.Pro852Ser) c.1920+214C>T (n.1920+214C>T) n.3022C>T c.2134C>T (p.Pro712Ser) c.1351C>T (p.Pro451Ser) c.2545C>T (p.Pro849Ser) | |
| 9 | g.91723940G>C | CA373793830 | ROR2 | c.2554C>G (p.Pro852Ala) c.1920+214C>G (n.1920+214C>G) n.3022C>G c.2134C>G (p.Pro712Ala) c.1351C>G (p.Pro451Ala) c.2545C>G (p.Pro849Ala) | |
| 9 | g.91723940G>T | CA373793825 | ROR2 | c.2554C>A (p.Pro852Thr) c.1920+214C>A (n.1920+214C>A) n.3022C>A c.2134C>A (p.Pro712Thr) c.1351C>A (p.Pro451Thr) c.2545C>A (p.Pro849Thr) | |
| 9 | g.91723941C>A | CA466334551 | ROR2 | c.2553G>T (p.Val851=) c.1920+213G>T (n.1920+213G>T) n.3021G>T c.2133G>T (p.Val711=) c.1350G>T (p.Val450=) c.2544G>T (p.Val848=) | |
| 9 | g.91723941C= | CA1863921780 | ROR2 | c.2553G= (p.Val851=) c.1920+213G= (n.1920+213G=) n.3021G= c.2133G= (p.Val711=) c.1350G= (p.Val450=) c.2544G= (p.Val848=) | |
| 9 | g.91723941C>G | CA466334552 | ROR2 | c.2553G>C (p.Val851=) c.1920+213G>C (n.1920+213G>C) n.3021G>C c.2133G>C (p.Val711=) c.1350G>C (p.Val450=) c.2544G>C (p.Val848=) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 9 | g.91723941C>T | CA195321747 | ROR2 | c.2553G>A (p.Val851=) c.1920+213G>A (n.1920+213G>A) n.3021G>A c.2133G>A (p.Val711=) c.1350G>A (p.Val450=) c.2544G>A (p.Val848=) | dbSNP gnomAD v2 gnomAD v4 |
| 9 | g.91723942A>C | CA373793841 | ROR2 | c.2552T>G (p.Val851Gly) c.1920+212T>G (n.1920+212T>G) n.3020T>G c.2132T>G (p.Val711Gly) c.1349T>G (p.Val450Gly) c.2543T>G (p.Val848Gly) | |
| 9 | g.91723942A>G | CA373793844 | ROR2 | c.2552T>C (p.Val851Ala) c.1920+212T>C (n.1920+212T>C) n.3020T>C c.2132T>C (p.Val711Ala) c.1349T>C (p.Val450Ala) c.2543T>C (p.Val848Ala) | |
| 9 | g.91723942A>T | CA373793843 | ROR2 | c.2552T>A (p.Val851Glu) c.1920+212T>A (n.1920+212T>A) n.3020T>A c.2132T>A (p.Val711Glu) c.1349T>A (p.Val450Glu) c.2543T>A (p.Val848Glu) | |
| 9 | g.91723943C>A | CA373793846 | ROR2 | c.2551G>T (p.Val851Leu) c.1920+211G>T (n.1920+211G>T) n.3019G>T c.2131G>T (p.Val711Leu) c.1348G>T (p.Val450Leu) c.2542G>T (p.Val848Leu) | dbSNP gnomAD v3 gnomAD v4 |
| 9 | g.91723943C= | CA1863921781 | ROR2 | c.2551G= (p.Val851=) c.1920+211G= (n.1920+211G=) n.3019G= c.2131G= (p.Val711=) c.1348G= (p.Val450=) c.2542G= (p.Val848=) | |
| 9 | g.91723943C>G | CA373793848 | ROR2 | c.2551G>C (p.Val851Leu) c.1920+211G>C (n.1920+211G>C) n.3019G>C c.2131G>C (p.Val711Leu) c.1348G>C (p.Val450Leu) c.2542G>C (p.Val848Leu) | |
| 9 | g.91723943C>T | CA373793850 | ROR2 | c.2551G>A (p.Val851Met) c.1920+211G>A (n.1920+211G>A) n.3019G>A c.2131G>A (p.Val711Met) c.1348G>A (p.Val450Met) c.2542G>A (p.Val848Met) | |
| 9 | g.91723944C>A | CA373793854 | ROR2 | c.2550G>T (p.Gln850His) c.1920+210G>T (n.1920+210G>T) n.3018G>T c.2130G>T (p.Gln710His) c.1347G>T (p.Gln449His) c.2541G>T (p.Gln847His) | |
| 9 | g.91723944C= | CA1863921782 | ROR2 | c.2550G= (p.Gln850=) c.1920+210G= (n.1920+210G=) n.3018G= c.2130G= (p.Gln710=) c.1347G= (p.Gln449=) c.2541G= (p.Gln847=) | |
| 9 | g.91723944C>G | CA373793857 | ROR2 | c.2550G>C (p.Gln850His) c.1920+210G>C (n.1920+210G>C) n.3018G>C c.2130G>C (p.Gln710His) c.1347G>C (p.Gln449His) c.2541G>C (p.Gln847His) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 9 | g.91723944C>T | CA466334553 | ROR2 | c.2550G>A (p.Gln850=) c.1920+210G>A (n.1920+210G>A) n.3018G>A c.2130G>A (p.Gln710=) c.1347G>A (p.Gln449=) c.2541G>A (p.Gln847=) | |
| 9 | g.91723945T>A | CA373793859 | ROR2 | c.2549A>T (p.Gln850Leu) c.1920+209A>T (n.1920+209A>T) n.3017A>T c.2129A>T (p.Gln710Leu) c.1346A>T (p.Gln449Leu) c.2540A>T (p.Gln847Leu) | ClinVar |
| 9 | g.91723945T>C | CA373793861 | ROR2 | c.2549A>G (p.Gln850Arg) c.1920+209A>G (n.1920+209A>G) n.3017A>G c.2129A>G (p.Gln710Arg) c.1346A>G (p.Gln449Arg) c.2540A>G (p.Gln847Arg) | dbSNP gnomAD v3 gnomAD v4 |
| 9 | g.91723945T>G | CA373793865 | ROR2 | c.2549A>C (p.Gln850Pro) c.1920+209A>C (n.1920+209A>C) n.3017A>C c.2129A>C (p.Gln710Pro) c.1346A>C (p.Gln449Pro) c.2540A>C (p.Gln847Pro) | gnomAD v4 |
| 9 | g.91723945T= | CA1863921783 | ROR2 | c.2549A= (p.Gln850=) c.1920+209A= (n.1920+209A=) n.3017A= c.2129A= (p.Gln710=) c.1346A= (p.Gln449=) c.2540A= (p.Gln847=) | |
| 9 | g.91723946G>A | CA373793869 | ROR2 | c.2548C>T (p.Gln850Ter) c.1920+208C>T (n.1920+208C>T) n.3016C>T c.2128C>T (p.Gln710Ter) c.1345C>T (p.Gln449Ter) c.2539C>T (p.Gln847Ter) | |
| 9 | g.91723946G>C | CA373793872 | ROR2 | c.2548C>G (p.Gln850Glu) c.1920+208C>G (n.1920+208C>G) n.3016C>G c.2128C>G (p.Gln710Glu) c.1345C>G (p.Gln449Glu) c.2539C>G (p.Gln847Glu) | |
| 9 | g.91723946G= | CA1863921784 | ROR2 | c.2548C= (p.Gln850=) c.1920+208C= (n.1920+208C=) n.3016C= c.2128C= (p.Gln710=) c.1345C= (p.Gln449=) c.2539C= (p.Gln847=) | |
| 9 | g.91723946G>T | CA5120362 | ROR2 | c.2548C>A (p.Gln850Lys) c.1920+208C>A (n.1920+208C>A) n.3016C>A c.2128C>A (p.Gln710Lys) c.1345C>A (p.Gln449Lys) c.2539C>A (p.Gln847Lys) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 9 | g.91723947C>A | CA373793876 | ROR2 | c.2547G>T (p.Gln849His) c.1920+207G>T (n.1920+207G>T) n.3015G>T c.2127G>T (p.Gln709His) c.1344G>T (p.Gln448His) c.2538G>T (p.Gln846His) | |
| 9 | g.91723947C>G | CA373793878 | ROR2 | c.2547G>C (p.Gln849His) c.1920+207G>C (n.1920+207G>C) n.3015G>C c.2127G>C (p.Gln709His) c.1344G>C (p.Gln448His) c.2538G>C (p.Gln846His) | |
| 9 | g.91723947C>T | CA466334554 | ROR2 | c.2547G>A (p.Gln849=) c.1920+207G>A (n.1920+207G>A) n.3015G>A c.2127G>A (p.Gln709=) c.1344G>A (p.Gln448=) c.2538G>A (p.Gln846=) | |
| 9 | g.91723948T>A | CA373793881 | ROR2 | c.2546A>T (p.Gln849Leu) c.1920+206A>T (n.1920+206A>T) n.3014A>T c.2126A>T (p.Gln709Leu) c.1343A>T (p.Gln448Leu) c.2537A>T (p.Gln846Leu) | |
| 9 | g.91723948T>C | CA373793884 | ROR2 | c.2546A>G (p.Gln849Arg) c.1920+206A>G (n.1920+206A>G) n.3014A>G c.2126A>G (p.Gln709Arg) c.1343A>G (p.Gln448Arg) c.2537A>G (p.Gln846Arg) | |
| 9 | g.91723948T>G | CA373793882 | ROR2 | c.2546A>C (p.Gln849Pro) c.1920+206A>C (n.1920+206A>C) n.3014A>C c.2126A>C (p.Gln709Pro) c.1343A>C (p.Gln448Pro) c.2537A>C (p.Gln846Pro) | |
| 9 | g.91723949G>A | CA373793887 | ROR2 | c.2545C>T (p.Gln849Ter) c.1920+205C>T (n.1920+205C>T) n.3013C>T c.2125C>T (p.Gln709Ter) c.1342C>T (p.Gln448Ter) c.2536C>T (p.Gln846Ter) | |
| 9 | g.91723949G>C | CA373793891 | ROR2 | c.2545C>G (p.Gln849Glu) c.1920+205C>G (n.1920+205C>G) n.3013C>G c.2125C>G (p.Gln709Glu) c.1342C>G (p.Gln448Glu) c.2536C>G (p.Gln846Glu) | |
| 9 | g.91723949G>T | CA373793893 | ROR2 | c.2545C>A (p.Gln849Lys) c.1920+205C>A (n.1920+205C>A) n.3013C>A c.2125C>A (p.Gln709Lys) c.1342C>A (p.Gln448Lys) c.2536C>A (p.Gln846Lys) | |
| 9 | g.91723950C>A | CA466334555 | ROR2 | c.2544G>T (p.Pro848=) c.1920+204G>T (n.1920+204G>T) n.3012G>T c.2124G>T (p.Pro708=) c.1341G>T (p.Pro447=) c.2535G>T (p.Pro845=) | |
| 9 | g.91723950C= | CA1863921788 | ROR2 | c.2544G= (p.Pro848=) c.1920+204G= (n.1920+204G=) n.3012G= c.2124G= (p.Pro708=) c.1341G= (p.Pro447=) c.2535G= (p.Pro845=) | |
| 9 | g.91723950C>G | CA466334556 | ROR2 | c.2544G>C (p.Pro848=) c.1920+204G>C (n.1920+204G>C) n.3012G>C c.2124G>C (p.Pro708=) c.1341G>C (p.Pro447=) c.2535G>C (p.Pro845=) | |
| 9 | g.91723950C>T | CA5120363 | ROR2 | c.2544G>A (p.Pro848=) c.1920+204G>A (n.1920+204G>A) n.3012G>A c.2124G>A (p.Pro708=) c.1341G>A (p.Pro447=) c.2535G>A (p.Pro845=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 9 | g.91723951G>A | CA5120364 | ROR2 | c.2543C>T (p.Pro848Leu) c.1920+203C>T (n.1920+203C>T) n.3011C>T c.2123C>T (p.Pro708Leu) c.1340C>T (p.Pro447Leu) c.2534C>T (p.Pro845Leu) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 9 | g.91723951G>C | CA373793907 | ROR2 | c.2543C>G (p.Pro848Arg) c.1920+203C>G (n.1920+203C>G) n.3011C>G c.2123C>G (p.Pro708Arg) c.1340C>G (p.Pro447Arg) c.2534C>G (p.Pro845Arg) | |
| 9 | g.91723951G= | CA1863921797 | ROR2 | c.2543C= (p.Pro848=) c.1920+203C= (n.1920+203C=) n.3011C= c.2123C= (p.Pro708=) c.1340C= (p.Pro447=) c.2534C= (p.Pro845=) | |
| 9 | g.91723951G>T | CA373793911 | ROR2 | c.2543C>A (p.Pro848Gln) c.1920+203C>A (n.1920+203C>A) n.3011C>A c.2123C>A (p.Pro708Gln) c.1340C>A (p.Pro447Gln) c.2534C>A (p.Pro845Gln) | |
| 9 | g.91723952G>A | CA373793916 | ROR2 | c.2542C>T (p.Pro848Ser) c.1920+202C>T (n.1920+202C>T) n.3010C>T c.2122C>T (p.Pro708Ser) c.1339C>T (p.Pro447Ser) c.2533C>T (p.Pro845Ser) | dbSNP |