| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 2 | g.29222332_29222333del | CA1241090499 | ALK | c.3515+16_3515+17del (n.3515+16_3515+17del) c.742+16_742+17del n.392+16_392+17del c.311+16_311+17del (n.311+16_311+17del) c.395+16_395+17del (n.395+16_395+17del) c.209+16_209+17del (n.209+16_209+17del) c.2384+16_2384+17del (n.2384+16_2384+17del) c.668+16_668+17del (n.668+16_668+17del) | ClinVar dbSNP gnomAD v4 |
| 2 | g.29222332C>A | CA2698999543 | ALK | c.3515+12G>T (n.3515+12G>T) c.742+12G>T n.392+12G>T c.311+12G>T (n.311+12G>T) c.395+12G>T (n.395+12G>T) c.209+12G>T (n.209+12G>T) c.2384+12G>T (n.2384+12G>T) c.668+12G>T (n.668+12G>T) | dbSNP |
| 2 | g.29222332C>G | CA2698999542 | ALK | c.3515+12G>C (n.3515+12G>C) c.742+12G>C n.392+12G>C c.311+12G>C (n.311+12G>C) c.395+12G>C (n.395+12G>C) c.209+12G>C (n.209+12G>C) c.2384+12G>C (n.2384+12G>C) c.668+12G>C (n.668+12G>C) | dbSNP |
| 2 | g.29222332C>T | CA2580066292 | ALK | c.3515+12G>A (n.3515+12G>A) c.742+12G>A n.392+12G>A c.311+12G>A (n.311+12G>A) c.395+12G>A (n.395+12G>A) c.209+12G>A (n.209+12G>A) c.2384+12G>A (n.2384+12G>A) c.668+12G>A (n.668+12G>A) | ClinVar dbSNP |
| 2 | g.29222333T>A | CA1241090505 | ALK | c.3515+11A>T (n.3515+11A>T) c.742+11A>T n.392+11A>T c.311+11A>T (n.311+11A>T) c.395+11A>T (n.395+11A>T) c.209+11A>T (n.209+11A>T) c.2384+11A>T (n.2384+11A>T) c.668+11A>T (n.668+11A>T) | dbSNP |
| 2 | g.29222333T>C | CA2698823703 | ALK | c.3515+11A>G (n.3515+11A>G) c.742+11A>G n.392+11A>G c.311+11A>G (n.311+11A>G) c.395+11A>G (n.395+11A>G) c.209+11A>G (n.209+11A>G) c.2384+11A>G (n.2384+11A>G) c.668+11A>G (n.668+11A>G) | dbSNP |
| 2 | g.29222333T= | CA1241090504 | ALK | c.3515+11A= (n.3515+11A=) c.742+11A= n.392+11A= c.311+11A= (n.311+11A=) c.395+11A= (n.395+11A=) c.209+11A= (n.209+11A=) c.2384+11A= (n.2384+11A=) c.668+11A= (n.668+11A=) | |
| 2 | g.29222334G>A | CA2698999545 | ALK | c.3515+10C>T (n.3515+10C>T) c.742+10C>T n.392+10C>T c.311+10C>T (n.311+10C>T) c.395+10C>T (n.395+10C>T) c.209+10C>T (n.209+10C>T) c.2384+10C>T (n.2384+10C>T) c.668+10C>T (n.668+10C>T) | dbSNP |
| 2 | g.29222334G>C | CA2698999546 | ALK | c.3515+10C>G (n.3515+10C>G) c.742+10C>G n.392+10C>G c.311+10C>G (n.311+10C>G) c.395+10C>G (n.395+10C>G) c.209+10C>G (n.209+10C>G) c.2384+10C>G (n.2384+10C>G) c.668+10C>G (n.668+10C>G) | dbSNP |
| 2 | g.29222335T>A | CA2698999549 | ALK | c.3515+9A>T (n.3515+9A>T) c.742+9A>T n.392+9A>T c.311+9A>T (n.311+9A>T) c.395+9A>T (n.395+9A>T) c.209+9A>T (n.209+9A>T) c.2384+9A>T (n.2384+9A>T) c.668+9A>T (n.668+9A>T) | dbSNP |
| 2 | g.29222335T>C | CA2658458271 | ALK | c.3515+9A>G (n.3515+9A>G) c.742+9A>G n.392+9A>G c.311+9A>G (n.311+9A>G) c.395+9A>G (n.395+9A>G) c.209+9A>G (n.209+9A>G) c.2384+9A>G (n.2384+9A>G) c.668+9A>G (n.668+9A>G) | gnomAD v4 |
| 2 | g.29222335T>G | CA2658458272 | ALK | c.3515+9A>C (n.3515+9A>C) c.742+9A>C n.392+9A>C c.311+9A>C (n.311+9A>C) c.395+9A>C (n.395+9A>C) c.209+9A>C (n.209+9A>C) c.2384+9A>C (n.2384+9A>C) c.668+9A>C (n.668+9A>C) | gnomAD v4 |
| 2 | g.29222336G>A | CA2698999551 | ALK | c.3515+8C>T (n.3515+8C>T) c.742+8C>T n.392+8C>T c.311+8C>T (n.311+8C>T) c.395+8C>T (n.395+8C>T) c.209+8C>T (n.209+8C>T) c.2384+8C>T (n.2384+8C>T) c.668+8C>T (n.668+8C>T) | dbSNP |
| 2 | g.29222336G>C | CA2576925294 | ALK | c.3515+8C>G (n.3515+8C>G) c.742+8C>G n.392+8C>G c.311+8C>G (n.311+8C>G) c.395+8C>G (n.395+8C>G) c.209+8C>G (n.209+8C>G) c.2384+8C>G (n.2384+8C>G) c.668+8C>G (n.668+8C>G) | dbSNP |
| 2 | g.29222336G>T | CA2698999552 | ALK | c.3515+8C>A (n.3515+8C>A) c.742+8C>A n.392+8C>A c.311+8C>A (n.311+8C>A) c.395+8C>A (n.395+8C>A) c.209+8C>A (n.209+8C>A) c.2384+8C>A (n.2384+8C>A) c.668+8C>A (n.668+8C>A) | dbSNP |
| 2 | g.29222337G>A | CA2698999556 | ALK | c.3515+7C>T (n.3515+7C>T) c.742+7C>T n.392+7C>T c.311+7C>T (n.311+7C>T) c.395+7C>T (n.395+7C>T) c.209+7C>T (n.209+7C>T) c.2384+7C>T (n.2384+7C>T) c.668+7C>T (n.668+7C>T) | dbSNP |
| 2 | g.29222337G>C | CA2698999554 | ALK | c.3515+7C>G (n.3515+7C>G) c.742+7C>G n.392+7C>G c.311+7C>G (n.311+7C>G) c.395+7C>G (n.395+7C>G) c.209+7C>G (n.209+7C>G) c.2384+7C>G (n.2384+7C>G) c.668+7C>G (n.668+7C>G) | dbSNP |
| 2 | g.29222337G>T | CA2697547995 | ALK | c.3515+7C>A (n.3515+7C>A) c.742+7C>A n.392+7C>A c.311+7C>A (n.311+7C>A) c.395+7C>A (n.395+7C>A) c.209+7C>A (n.209+7C>A) c.2384+7C>A (n.2384+7C>A) c.668+7C>A (n.668+7C>A) | ClinVar dbSNP |
| 2 | g.29222339T>A | CA2698999557 | ALK | c.3515+5A>T (n.3515+5A>T) c.742+5A>T n.392+5A>T c.311+5A>T (n.311+5A>T) c.395+5A>T (n.395+5A>T) c.209+5A>T (n.209+5A>T) c.2384+5A>T (n.2384+5A>T) c.668+5A>T (n.668+5A>T) | dbSNP |
| 2 | g.29222340T>A | CA2658458273 | ALK | c.3515+4A>T (n.3515+4A>T) c.742+4A>T n.392+4A>T c.311+4A>T (n.311+4A>T) c.395+4A>T (n.395+4A>T) c.209+4A>T (n.209+4A>T) c.2384+4A>T (n.2384+4A>T) c.668+4A>T (n.668+4A>T) | dbSNP gnomAD v4 |
| 2 | g.29222340T>C | CA2698999559 | ALK | c.3515+4A>G (n.3515+4A>G) c.742+4A>G n.392+4A>G c.311+4A>G (n.311+4A>G) c.395+4A>G (n.395+4A>G) c.209+4A>G (n.209+4A>G) c.2384+4A>G (n.2384+4A>G) c.668+4A>G (n.668+4A>G) | dbSNP |
| 2 | g.29222341T>A | CA2698999561 | ALK | c.3515+3A>T (n.3515+3A>T) c.742+3A>T n.392+3A>T c.311+3A>T (n.311+3A>T) c.395+3A>T (n.395+3A>T) c.209+3A>T (n.209+3A>T) c.2384+3A>T (n.2384+3A>T) c.668+3A>T (n.668+3A>T) | dbSNP |
| 2 | g.29222341T>G | CA2698999563 | ALK | c.3515+3A>C (n.3515+3A>C) c.742+3A>C n.392+3A>C c.311+3A>C (n.311+3A>C) c.395+3A>C (n.395+3A>C) c.209+3A>C (n.209+3A>C) c.2384+3A>C (n.2384+3A>C) c.668+3A>C (n.668+3A>C) | dbSNP |
| 2 | g.29222342A>C | CA346462845 | ALK | c.3515+2T>G (n.3515+2T>G) c.742+2T>G n.392+2T>G c.311+2T>G (n.311+2T>G) c.395+2T>G (n.395+2T>G) c.209+2T>G (n.209+2T>G) c.2384+2T>G (n.2384+2T>G) c.668+2T>G (n.668+2T>G) | dbSNP |
| 2 | g.29222342A>G | CA346462837 | ALK | c.3515+2T>C (n.3515+2T>C) c.742+2T>C n.392+2T>C c.311+2T>C (n.311+2T>C) c.395+2T>C (n.395+2T>C) c.209+2T>C (n.209+2T>C) c.2384+2T>C (n.2384+2T>C) c.668+2T>C (n.668+2T>C) | ClinVar dbSNP |
| 2 | g.29222342A>T | CA346462841 | ALK | c.3515+2T>A (n.3515+2T>A) c.742+2T>A n.392+2T>A c.311+2T>A (n.311+2T>A) c.395+2T>A (n.395+2T>A) c.209+2T>A (n.209+2T>A) c.2384+2T>A (n.2384+2T>A) c.668+2T>A (n.668+2T>A) | dbSNP |
| 2 | g.29222343C>A | CA346462849 | ALK | c.3515+1G>T (n.3515+1G>T) c.742+1G>T n.392+1G>T c.311+1G>T (n.311+1G>T) c.395+1G>T (n.395+1G>T) c.209+1G>T (n.209+1G>T) c.2384+1G>T (n.2384+1G>T) c.668+1G>T (n.668+1G>T) | |
| 2 | g.29222343C>G | CA346462851 | ALK | c.3515+1G>C (n.3515+1G>C) c.742+1G>C n.392+1G>C c.311+1G>C (n.311+1G>C) c.395+1G>C (n.395+1G>C) c.209+1G>C (n.209+1G>C) c.2384+1G>C (n.2384+1G>C) c.668+1G>C (n.668+1G>C) | |
| 2 | g.29222343C>T | CA346462858 | ALK | c.3515+1G>A (n.3515+1G>A) c.742+1G>A n.392+1G>A c.311+1G>A (n.311+1G>A) c.395+1G>A (n.395+1G>A) c.209+1G>A (n.209+1G>A) c.2384+1G>A (n.2384+1G>A) c.668+1G>A (n.668+1G>A) | COSMIC |
| 2 | g.29222344C>A | CA346462861 | ALK | c.3515G>T (p.Ser1172Ile) c.742G>T n.392G>T c.311G>T (p.Ser104Ile) c.395G>T (p.Ser132Ile) c.209G>T (p.Ser70Ile) c.2384G>T (p.Ser795Ile) c.668G>T (p.Ser223Ile) | dbSNP |
| 2 | g.29222344C>G | CA346462863 | ALK | c.3515G>C (p.Ser1172Thr) c.742G>C n.392G>C c.311G>C (p.Ser104Thr) c.395G>C (p.Ser132Thr) c.209G>C (p.Ser70Thr) c.2384G>C (p.Ser795Thr) c.668G>C (p.Ser223Thr) | dbSNP |
| 2 | g.29222344C>T | CA346462867 | ALK | c.3515G>A (p.Ser1172Asn) c.742G>A n.392G>A c.311G>A (p.Ser104Asn) c.395G>A (p.Ser132Asn) c.209G>A (p.Ser70Asn) c.2384G>A (p.Ser795Asn) c.668G>A (p.Ser223Asn) | dbSNP gnomAD v4 |
| 2 | g.29222345T>A | CA346462870 | ALK | c.3514A>T (p.Ser1172Cys) c.741A>T n.391A>T c.310A>T (p.Ser104Cys) c.394A>T (p.Ser132Cys) c.208A>T (p.Ser70Cys) c.2383A>T (p.Ser795Cys) c.667A>T (p.Ser223Cys) | ClinVar dbSNP gnomAD v4 |
| 2 | g.29222345T>C | CA346462871 | ALK | c.3514A>G (p.Ser1172Gly) c.741A>G n.391A>G c.310A>G (p.Ser104Gly) c.394A>G (p.Ser132Gly) c.208A>G (p.Ser70Gly) c.2383A>G (p.Ser795Gly) c.667A>G (p.Ser223Gly) | dbSNP |
| 2 | g.29222345T>G | CA346462875 | ALK | c.3514A>C (p.Ser1172Arg) c.741A>C n.391A>C c.310A>C (p.Ser104Arg) c.394A>C (p.Ser132Arg) c.208A>C (p.Ser70Arg) c.2383A>C (p.Ser795Arg) c.667A>C (p.Ser223Arg) | ClinVar dbSNP |
| 2 | g.29222345T= | CA1241090506 | ALK | c.3514A= (p.Ser1172=) c.741A= n.391A= c.310A= (p.Ser104=) c.394A= (p.Ser132=) c.208A= (p.Ser70=) c.2383A= (p.Ser795=) c.667A= (p.Ser223=) | |
| 2 | g.29222346G>A | CA425434554 | ALK | c.3513C>T (p.Ile1171=) c.740C>T n.390C>T c.309C>T (p.Ile103=) c.393C>T (p.Ile131=) c.207C>T (p.Ile69=) c.2382C>T (p.Ile794=) c.666C>T (p.Ile222=) | ClinVar dbSNP |
| 2 | g.29222346G>C | CA1593919 | ALK | c.3513C>G (p.Ile1171Met) c.740C>G n.390C>G c.309C>G (p.Ile103Met) c.393C>G (p.Ile131Met) c.207C>G (p.Ile69Met) c.2382C>G (p.Ile794Met) c.666C>G (p.Ile222Met) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 2 | g.29222346G= | CA1241090507 | ALK | c.3513C= (p.Ile1171=) c.740C= n.390C= c.309C= (p.Ile103=) c.393C= (p.Ile131=) c.207C= (p.Ile69=) c.2382C= (p.Ile794=) c.666C= (p.Ile222=) | |
| 2 | g.29222346G>T | CA425434555 | ALK | c.3513C>A (p.Ile1171=) c.740C>A n.390C>A c.309C>A (p.Ile103=) c.393C>A (p.Ile131=) c.207C>A (p.Ile69=) c.2382C>A (p.Ile794=) c.666C>A (p.Ile222=) | dbSNP COSMIC |
| 2 | g.29222346_29222347delinsAT | CA645528800 | ALK | c.3512_3513delinsAT (p.Ile1171Asn) c.739_740delinsAT n.389_390delinsAT c.308_309delinsAT (p.Ile103Asn) c.392_393delinsAT (p.Ile131Asn) c.206_207delinsAT (p.Ile69Asn) c.2381_2382delinsAT (p.Ile794Asn) c.665_666delinsAT (p.Ile222Asn) | dbSNP COSMIC |
| 2 | g.29222347A= | CA1241090508 | ALK | c.3512T= (p.Ile1171=) c.739T= n.389T= c.308T= (p.Ile103=) c.392T= (p.Ile131=) c.206T= (p.Ile69=) c.2381T= (p.Ile794=) c.665T= (p.Ile222=) | |
| 2 | g.29222347A>C | CA346462883 | ALK | c.3512T>G (p.Ile1171Ser) c.739T>G n.389T>G c.308T>G (p.Ile103Ser) c.392T>G (p.Ile131Ser) c.206T>G (p.Ile69Ser) c.2381T>G (p.Ile794Ser) c.665T>G (p.Ile222Ser) | dbSNP COSMIC |
| 2 | g.29222347A>G | CA346462880 | ALK | c.3512T>C (p.Ile1171Thr) c.739T>C n.389T>C c.308T>C (p.Ile103Thr) c.392T>C (p.Ile131Thr) c.206T>C (p.Ile69Thr) c.2381T>C (p.Ile794Thr) c.665T>C (p.Ile222Thr) | ClinVar dbSNP COSMIC |
| 2 | g.29222347A>T | CA16602371 | ALK | c.3512T>A (p.Ile1171Asn) c.739T>A n.389T>A c.308T>A (p.Ile103Asn) c.392T>A (p.Ile131Asn) c.206T>A (p.Ile69Asn) c.2381T>A (p.Ile794Asn) c.665T>A (p.Ile222Asn) | ClinVar dbSNP COSMIC |
| 2 | g.29222347_29222348delinsTG | CA2698999587 | ALK | c.3511_3512delinsCA (p.Ile1171His) c.738_739delinsCA n.388_389delinsCA c.307_308delinsCA (p.Ile103His) c.391_392delinsCA (p.Ile131His) c.205_206delinsCA (p.Ile69His) c.2380_2381delinsCA (p.Ile794His) c.664_665delinsCA (p.Ile222His) | dbSNP |
| 2 | g.29222348T>A | CA346462885 | ALK | c.3511A>T (p.Ile1171Phe) c.738A>T n.388A>T c.307A>T (p.Ile103Phe) c.391A>T (p.Ile131Phe) c.205A>T (p.Ile69Phe) c.2380A>T (p.Ile794Phe) c.664A>T (p.Ile222Phe) | dbSNP |
| 2 | g.29222348T>C | CA346462887 | ALK | c.3511A>G (p.Ile1171Val) c.738A>G n.388A>G c.307A>G (p.Ile103Val) c.391A>G (p.Ile131Val) c.205A>G (p.Ile69Val) c.2380A>G (p.Ile794Val) c.664A>G (p.Ile222Val) | dbSNP gnomAD v4 |
| 2 | g.29222348T>G | CA346462891 | ALK | c.3511A>C (p.Ile1171Leu) c.738A>C n.388A>C c.307A>C (p.Ile103Leu) c.391A>C (p.Ile131Leu) c.205A>C (p.Ile69Leu) c.2380A>C (p.Ile794Leu) c.664A>C (p.Ile222Leu) | dbSNP |
| 2 | g.29222349G>A | CA425434556 | ALK | c.3510C>T (p.Ile1170=) c.737C>T n.387C>T c.306C>T (p.Ile102=) c.390C>T (p.Ile130=) c.204C>T (p.Ile68=) c.2379C>T (p.Ile793=) c.663C>T (p.Ile221=) | dbSNP |
| 2 | g.29222349G>C | CA44631173 | ALK | c.3510C>G (p.Ile1170Met) c.737C>G n.387C>G c.306C>G (p.Ile102Met) c.390C>G (p.Ile130Met) c.204C>G (p.Ile68Met) c.2379C>G (p.Ile793Met) c.663C>G (p.Ile221Met) | dbSNP gnomAD v3 gnomAD v4 |
| 2 | g.29222349G= | CA1241090509 | ALK | c.3510C= (p.Ile1170=) c.737C= n.387C= c.306C= (p.Ile102=) c.390C= (p.Ile130=) c.204C= (p.Ile68=) c.2379C= (p.Ile793=) c.663C= (p.Ile221=) | |
| 2 | g.29222349G>T | CA425434557 | ALK | c.3510C>A (p.Ile1170=) c.737C>A n.387C>A c.306C>A (p.Ile102=) c.390C>A (p.Ile130=) c.204C>A (p.Ile68=) c.2379C>A (p.Ile793=) c.663C>A (p.Ile221=) | |
| 2 | g.29222349_29222352delinsGATC | CA1241090510 | ALK | c.3507_3510delinsGATC (p.Leu1169=) c.734_737delinsGATC n.384_387delinsGATC c.303_306delinsGATC (p.Leu101=) c.387_390delinsGATC (p.Leu129=) c.201_204delinsGATC (p.Leu67=) c.2376_2379delinsGATC (p.Leu792=) c.660_663delinsGATC (p.Leu220=) | |
| 2 | g.29222350A= | CA1241090511 | ALK | c.3509T= (p.Ile1170=) c.736T= n.386T= c.305T= (p.Ile102=) c.389T= (p.Ile130=) c.203T= (p.Ile68=) c.2378T= (p.Ile793=) c.662T= (p.Ile221=) | |
| 2 | g.29222350A>C | CA346462896 | ALK | c.3509T>G (p.Ile1170Ser) c.736T>G n.386T>G c.305T>G (p.Ile102Ser) c.389T>G (p.Ile130Ser) c.203T>G (p.Ile68Ser) c.2378T>G (p.Ile793Ser) c.662T>G (p.Ile221Ser) | COSMIC |
| 2 | g.29222350A>G | CA346462900 | ALK | c.3509T>C (p.Ile1170Thr) c.736T>C n.386T>C c.305T>C (p.Ile102Thr) c.389T>C (p.Ile130Thr) c.203T>C (p.Ile68Thr) c.2378T>C (p.Ile793Thr) c.662T>C (p.Ile221Thr) | COSMIC |
| 2 | g.29222350A>T | CA346462902 | ALK | c.3509T>A (p.Ile1170Asn) c.736T>A n.386T>A c.305T>A (p.Ile102Asn) c.389T>A (p.Ile130Asn) c.203T>A (p.Ile68Asn) c.2378T>A (p.Ile793Asn) c.662T>A (p.Ile221Asn) | ClinVar dbSNP COSMIC |
| 2 | g.29222351_29222353del | CA1593920 | ALK | c.3507_3509del (p.Ile1170del) c.734_736del n.384_386del c.303_305del (p.Ile102del) c.387_389del (p.Ile130del) c.201_203del (p.Ile68del) c.2376_2378del (p.Ile793del) c.660_662del (p.Ile221del) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 2 | g.29222351T>A | CA346462905 | ALK | c.3508A>T (p.Ile1170Phe) c.735A>T n.385A>T c.304A>T (p.Ile102Phe) c.388A>T (p.Ile130Phe) c.202A>T (p.Ile68Phe) c.2377A>T (p.Ile793Phe) c.661A>T (p.Ile221Phe) | dbSNP |
| 2 | g.29222351T>C | CA346462908 | ALK | c.3508A>G (p.Ile1170Val) c.735A>G n.385A>G c.304A>G (p.Ile102Val) c.388A>G (p.Ile130Val) c.202A>G (p.Ile68Val) c.2377A>G (p.Ile793Val) c.661A>G (p.Ile221Val) | |
| 2 | g.29222351T>G | CA346462911 | ALK | c.3508A>C (p.Ile1170Leu) c.735A>C n.385A>C c.304A>C (p.Ile102Leu) c.388A>C (p.Ile130Leu) c.202A>C (p.Ile68Leu) c.2377A>C (p.Ile793Leu) c.661A>C (p.Ile221Leu) | dbSNP |
| 2 | g.29222352C>A | CA425434560 | ALK | c.3507G>T (p.Leu1169=) c.734G>T n.384G>T c.303G>T (p.Leu101=) c.387G>T (p.Leu129=) c.201G>T (p.Leu67=) c.2376G>T (p.Leu792=) c.660G>T (p.Leu220=) | |
| 2 | g.29222352C>G | CA425434559 | ALK | c.3507G>C (p.Leu1169=) c.734G>C n.384G>C c.303G>C (p.Leu101=) c.387G>C (p.Leu129=) c.201G>C (p.Leu67=) c.2376G>C (p.Leu792=) c.660G>C (p.Leu220=) | dbSNP |
| 2 | g.29222352C>T | CA425434558 | ALK | c.3507G>A (p.Leu1169=) c.734G>A n.384G>A c.303G>A (p.Leu101=) c.387G>A (p.Leu129=) c.201G>A (p.Leu67=) c.2376G>A (p.Leu792=) c.660G>A (p.Leu220=) | ClinVar dbSNP |
| 2 | g.29222353A>C | CA346462919 | ALK | c.3506T>G (p.Leu1169Arg) c.733T>G n.383T>G c.302T>G (p.Leu101Arg) c.386T>G (p.Leu129Arg) c.200T>G (p.Leu67Arg) c.2375T>G (p.Leu792Arg) c.659T>G (p.Leu220Arg) | |
| 2 | g.29222353A>G | CA346462921 | ALK | c.3506T>C (p.Leu1169Pro) c.733T>C n.383T>C c.302T>C (p.Leu101Pro) c.386T>C (p.Leu129Pro) c.200T>C (p.Leu67Pro) c.2375T>C (p.Leu792Pro) c.659T>C (p.Leu220Pro) | dbSNP gnomAD v4 |
| 2 | g.29222353A>T | CA346462915 | ALK | c.3506T>A (p.Leu1169Gln) c.733T>A n.383T>A c.302T>A (p.Leu101Gln) c.386T>A (p.Leu129Gln) c.200T>A (p.Leu67Gln) c.2375T>A (p.Leu792Gln) c.659T>A (p.Leu220Gln) | dbSNP |
| 2 | g.29222354G>A | CA425434561 | ALK | c.3505C>T (p.Leu1169=) c.732C>T n.382C>T c.301C>T (p.Leu101=) c.385C>T (p.Leu129=) c.199C>T (p.Leu67=) c.2374C>T (p.Leu792=) c.658C>T (p.Leu220=) | dbSNP |
| 2 | g.29222354G>C | CA346462924 | ALK | c.3505C>G (p.Leu1169Val) c.732C>G n.382C>G c.301C>G (p.Leu101Val) c.385C>G (p.Leu129Val) c.199C>G (p.Leu67Val) c.2374C>G (p.Leu792Val) c.658C>G (p.Leu220Val) | dbSNP |
| 2 | g.29222354G>T | CA346462929 | ALK | c.3505C>A (p.Leu1169Met) c.732C>A n.382C>A c.301C>A (p.Leu101Met) c.385C>A (p.Leu129Met) c.199C>A (p.Leu67Met) c.2374C>A (p.Leu792Met) c.658C>A (p.Leu220Met) | |
| 2 | g.29222355G>A | CA425434562 | ALK | c.3504C>T (p.Ala1168=) c.731C>T n.381C>T c.300C>T (p.Ala100=) c.384C>T (p.Ala128=) c.198C>T (p.Ala66=) c.2373C>T (p.Ala791=) c.657C>T (p.Ala219=) | dbSNP |
| 2 | g.29222355G>C | CA425434563 | ALK | c.3504C>G (p.Ala1168=) c.731C>G n.381C>G c.300C>G (p.Ala100=) c.384C>G (p.Ala128=) c.198C>G (p.Ala66=) c.2373C>G (p.Ala791=) c.657C>G (p.Ala219=) | ClinVar dbSNP |
| 2 | g.29222355G= | CA1241090512 | ALK | c.3504C= (p.Ala1168=) c.731C= n.381C= c.300C= (p.Ala100=) c.384C= (p.Ala128=) c.198C= (p.Ala66=) c.2373C= (p.Ala791=) c.657C= (p.Ala219=) | |
| 2 | g.29222355G>T | CA425434564 | ALK | c.3504C>A (p.Ala1168=) c.731C>A n.381C>A c.300C>A (p.Ala100=) c.384C>A (p.Ala128=) c.198C>A (p.Ala66=) c.2373C>A (p.Ala791=) c.657C>A (p.Ala219=) | dbSNP gnomAD v4 |
| 2 | g.29222356G>A | CA346462932 | ALK | c.3503C>T (p.Ala1168Val) c.730C>T n.380C>T c.299C>T (p.Ala100Val) c.383C>T (p.Ala128Val) c.197C>T (p.Ala66Val) c.2372C>T (p.Ala791Val) c.656C>T (p.Ala219Val) | dbSNP |
| 2 | g.29222356G>C | CA346462940 | ALK | c.3503C>G (p.Ala1168Gly) c.730C>G n.380C>G c.299C>G (p.Ala100Gly) c.383C>G (p.Ala128Gly) c.197C>G (p.Ala66Gly) c.2372C>G (p.Ala791Gly) c.656C>G (p.Ala219Gly) | dbSNP |
| 2 | g.29222356G>T | CA346462945 | ALK | c.3503C>A (p.Ala1168Asp) c.730C>A n.380C>A c.299C>A (p.Ala100Asp) c.383C>A (p.Ala128Asp) c.197C>A (p.Ala66Asp) c.2372C>A (p.Ala791Asp) c.656C>A (p.Ala219Asp) | dbSNP |
| 2 | g.29222357C>A | CA346462949 | ALK | c.3502G>T (p.Ala1168Ser) c.729G>T n.379G>T c.298G>T (p.Ala100Ser) c.382G>T (p.Ala128Ser) c.196G>T (p.Ala66Ser) c.2371G>T (p.Ala791Ser) c.655G>T (p.Ala219Ser) | |
| 2 | g.29222357C>G | CA346462952 | ALK | c.3502G>C (p.Ala1168Pro) c.729G>C n.379G>C c.298G>C (p.Ala100Pro) c.382G>C (p.Ala128Pro) c.196G>C (p.Ala66Pro) c.2371G>C (p.Ala791Pro) c.655G>C (p.Ala219Pro) | dbSNP COSMIC |
| 2 | g.29222357C>T | CA346462953 | ALK | c.3502G>A (p.Ala1168Thr) c.729G>A n.379G>A c.298G>A (p.Ala100Thr) c.382G>A (p.Ala128Thr) c.196G>A (p.Ala66Thr) c.2371G>A (p.Ala791Thr) c.655G>A (p.Ala219Thr) | dbSNP |
| 2 | g.29222358T>A | CA346462958 | ALK | c.3501A>T (p.Glu1167Asp) c.728A>T n.378A>T c.297A>T (p.Glu99Asp) c.381A>T (p.Glu127Asp) c.195A>T (p.Glu65Asp) c.2370A>T (p.Glu790Asp) c.654A>T (p.Glu218Asp) | dbSNP |
| 2 | g.29222358T>C | CA425434565 | ALK | c.3501A>G (p.Glu1167=) c.728A>G n.378A>G c.297A>G (p.Glu99=) c.381A>G (p.Glu127=) c.195A>G (p.Glu65=) c.2370A>G (p.Glu790=) c.654A>G (p.Glu218=) | dbSNP |
| 2 | g.29222358T>G | CA346462966 | ALK | c.3501A>C (p.Glu1167Asp) c.728A>C n.378A>C c.297A>C (p.Glu99Asp) c.381A>C (p.Glu127Asp) c.195A>C (p.Glu65Asp) c.2370A>C (p.Glu790Asp) c.654A>C (p.Glu218Asp) | |
| 2 | g.29222359T>A | CA346462970 | ALK | c.3500A>T (p.Glu1167Val) c.727A>T n.377A>T c.296A>T (p.Glu99Val) c.380A>T (p.Glu127Val) c.194A>T (p.Glu65Val) c.2369A>T (p.Glu790Val) c.653A>T (p.Glu218Val) | |
| 2 | g.29222359T>C | CA346462972 | ALK | c.3500A>G (p.Glu1167Gly) c.727A>G n.377A>G c.296A>G (p.Glu99Gly) c.380A>G (p.Glu127Gly) c.194A>G (p.Glu65Gly) c.2369A>G (p.Glu790Gly) c.653A>G (p.Glu218Gly) | |
| 2 | g.29222359T>G | CA346462976 | ALK | c.3500A>C (p.Glu1167Ala) c.727A>C n.377A>C c.296A>C (p.Glu99Ala) c.380A>C (p.Glu127Ala) c.194A>C (p.Glu65Ala) c.2369A>C (p.Glu790Ala) c.653A>C (p.Glu218Ala) | |
| 2 | g.29222360C>A | CA346462984 | ALK | c.3499G>T (p.Glu1167Ter) c.726G>T n.376G>T c.295G>T (p.Glu99Ter) c.379G>T (p.Glu127Ter) c.193G>T (p.Glu65Ter) c.2368G>T (p.Glu790Ter) c.652G>T (p.Glu218Ter) | |
| 2 | g.29222360C>G | CA346462982 | ALK | c.3499G>C (p.Glu1167Gln) c.726G>C n.376G>C c.295G>C (p.Glu99Gln) c.379G>C (p.Glu127Gln) c.193G>C (p.Glu65Gln) c.2368G>C (p.Glu790Gln) c.652G>C (p.Glu218Gln) | |
| 2 | g.29222360C>T | CA346462978 | ALK | c.3499G>A (p.Glu1167Lys) c.726G>A n.376G>A c.295G>A (p.Glu99Lys) c.379G>A (p.Glu127Lys) c.193G>A (p.Glu65Lys) c.2368G>A (p.Glu790Lys) c.652G>A (p.Glu218Lys) | ClinVar COSMIC |
| 2 | g.29222361C>A | CA346462988 | ALK | c.3498G>T (p.Met1166Ile) c.725G>T n.375G>T c.294G>T (p.Met98Ile) c.378G>T (p.Met126Ile) c.192G>T (p.Met64Ile) c.2367G>T (p.Met789Ile) c.651G>T (p.Met217Ile) | |
| 2 | g.29222361C= | CA1241090513 | ALK | c.3498G= (p.Met1166=) c.725G= n.375G= c.294G= (p.Met98=) c.378G= (p.Met126=) c.192G= (p.Met64=) c.2367G= (p.Met789=) c.651G= (p.Met217=) | |
| 2 | g.29222361C>G | CA346462991 | ALK | c.3498G>C (p.Met1166Ile) c.725G>C n.375G>C c.294G>C (p.Met98Ile) c.378G>C (p.Met126Ile) c.192G>C (p.Met64Ile) c.2367G>C (p.Met789Ile) c.651G>C (p.Met217Ile) | dbSNP |
| 2 | g.29222361C>T | CA346462993 | ALK | c.3498G>A (p.Met1166Ile) c.725G>A n.375G>A c.294G>A (p.Met98Ile) c.378G>A (p.Met126Ile) c.192G>A (p.Met64Ile) c.2367G>A (p.Met789Ile) c.651G>A (p.Met217Ile) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 2 | g.29222361_29222362delinsAT | CA645528801 | ALK | c.3497_3498delinsAT (p.Met1166Asn) c.724_725delinsAT n.374_375delinsAT c.293_294delinsAT (p.Met98Asn) c.377_378delinsAT (p.Met126Asn) c.191_192delinsAT (p.Met64Asn) c.2366_2367delinsAT (p.Met789Asn) c.650_651delinsAT (p.Met217Asn) | COSMIC |
| 2 | g.29222362A= | CA1241090514 | ALK | c.3497T= (p.Met1166=) c.724T= n.374T= c.293T= (p.Met98=) c.377T= (p.Met126=) c.191T= (p.Met64=) c.2366T= (p.Met789=) c.650T= (p.Met217=) | |
| 2 | g.29222362A>C | CA16603123 | ALK | c.3497T>G (p.Met1166Arg) c.724T>G n.374T>G c.293T>G (p.Met98Arg) c.377T>G (p.Met126Arg) c.191T>G (p.Met64Arg) c.2366T>G (p.Met789Arg) c.650T>G (p.Met217Arg) | ClinVar dbSNP COSMIC |
| 2 | g.29222362A>G | CA346462997 | ALK | c.3497T>C (p.Met1166Thr) c.724T>C n.374T>C c.293T>C (p.Met98Thr) c.377T>C (p.Met126Thr) c.191T>C (p.Met64Thr) c.2366T>C (p.Met789Thr) c.650T>C (p.Met217Thr) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 2 | g.29222362A>T | CA346463000 | ALK | c.3497T>A (p.Met1166Lys) c.724T>A n.374T>A c.293T>A (p.Met98Lys) c.377T>A (p.Met126Lys) c.191T>A (p.Met64Lys) c.2366T>A (p.Met789Lys) c.650T>A (p.Met217Lys) | dbSNP |
| 2 | g.29222363T>A | CA346463005 | ALK | c.3496A>T (p.Met1166Leu) c.723A>T n.373A>T c.292A>T (p.Met98Leu) c.376A>T (p.Met126Leu) c.190A>T (p.Met64Leu) c.2365A>T (p.Met789Leu) c.649A>T (p.Met217Leu) | dbSNP |
| 2 | g.29222363T>C | CA346463007 | ALK | c.3496A>G (p.Met1166Val) c.723A>G n.373A>G c.292A>G (p.Met98Val) c.376A>G (p.Met126Val) c.190A>G (p.Met64Val) c.2365A>G (p.Met789Val) c.649A>G (p.Met217Val) | |
| 2 | g.29222363T>G | CA346463010 | ALK | c.3496A>C (p.Met1166Leu) c.723A>C n.373A>C c.292A>C (p.Met98Leu) c.376A>C (p.Met126Leu) c.190A>C (p.Met64Leu) c.2365A>C (p.Met789Leu) c.649A>C (p.Met217Leu) | dbSNP |
| 2 | g.29222364G>A | CA1593921 | ALK | c.3495C>T (p.Leu1165=) c.722C>T n.372C>T c.291C>T (p.Leu97=) c.375C>T (p.Leu125=) c.189C>T (p.Leu63=) c.2364C>T (p.Leu788=) c.648C>T (p.Leu216=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 2 | g.29222364G>C | CA425434567 | ALK | c.3495C>G (p.Leu1165=) c.722C>G n.372C>G c.291C>G (p.Leu97=) c.375C>G (p.Leu125=) c.189C>G (p.Leu63=) c.2364C>G (p.Leu788=) c.648C>G (p.Leu216=) | dbSNP |
| 2 | g.29222364G= | CA1241090515 | ALK | c.3495C= (p.Leu1165=) c.722C= n.372C= c.291C= (p.Leu97=) c.375C= (p.Leu125=) c.189C= (p.Leu63=) c.2364C= (p.Leu788=) c.648C= (p.Leu216=) | |
| 2 | g.29222364G>T | CA425434566 | ALK | c.3495C>A (p.Leu1165=) c.722C>A n.372C>A c.291C>A (p.Leu97=) c.375C>A (p.Leu125=) c.189C>A (p.Leu63=) c.2364C>A (p.Leu788=) c.648C>A (p.Leu216=) | |
| 2 | g.29222365A>C | CA346463016 | ALK | c.3494T>G (p.Leu1165Arg) c.721T>G n.371T>G c.290T>G (p.Leu97Arg) c.374T>G (p.Leu125Arg) c.188T>G (p.Leu63Arg) c.2363T>G (p.Leu788Arg) c.647T>G (p.Leu216Arg) | |
| 2 | g.29222365A>G | CA346463019 | ALK | c.3494T>C (p.Leu1165Pro) c.721T>C n.371T>C c.290T>C (p.Leu97Pro) c.374T>C (p.Leu125Pro) c.188T>C (p.Leu63Pro) c.2363T>C (p.Leu788Pro) c.647T>C (p.Leu216Pro) | |
| 2 | g.29222365A>T | CA346463020 | ALK | c.3494T>A (p.Leu1165His) c.721T>A n.371T>A c.290T>A (p.Leu97His) c.374T>A (p.Leu125His) c.188T>A (p.Leu63His) c.2363T>A (p.Leu788His) c.647T>A (p.Leu216His) | dbSNP |
| 2 | g.29222366G>A | CA346463026 | ALK | c.3493C>T (p.Leu1165Phe) c.720C>T n.370C>T c.289C>T (p.Leu97Phe) c.373C>T (p.Leu125Phe) c.187C>T (p.Leu63Phe) c.2362C>T (p.Leu788Phe) c.646C>T (p.Leu216Phe) | ClinVar dbSNP |
| 2 | g.29222366G>C | CA346463027 | ALK | c.3493C>G (p.Leu1165Val) c.720C>G n.370C>G c.289C>G (p.Leu97Val) c.373C>G (p.Leu125Val) c.187C>G (p.Leu63Val) c.2362C>G (p.Leu788Val) c.646C>G (p.Leu216Val) | |
| 2 | g.29222366G>T | CA346463024 | ALK | c.3493C>A (p.Leu1165Ile) c.720C>A n.370C>A c.289C>A (p.Leu97Ile) c.373C>A (p.Leu125Ile) c.187C>A (p.Leu63Ile) c.2362C>A (p.Leu788Ile) c.646C>A (p.Leu216Ile) | |
| 2 | g.29222367G>A | CA425434569 | ALK | c.3492C>T (p.Phe1164=) c.719C>T n.369C>T c.288C>T (p.Phe96=) c.372C>T (p.Phe124=) c.186C>T (p.Phe62=) c.2361C>T (p.Phe787=) c.645C>T (p.Phe215=) | ClinVar dbSNP COSMIC |
| 2 | g.29222367G>C | CA346463034 | ALK | c.3492C>G (p.Phe1164Leu) c.719C>G n.369C>G c.288C>G (p.Phe96Leu) c.372C>G (p.Phe124Leu) c.186C>G (p.Phe62Leu) c.2361C>G (p.Phe787Leu) c.645C>G (p.Phe215Leu) | dbSNP |
| 2 | g.29222367G>T | CA346463032 | ALK | c.3492C>A (p.Phe1164Leu) c.719C>A n.369C>A c.288C>A (p.Phe96Leu) c.372C>A (p.Phe124Leu) c.186C>A (p.Phe62Leu) c.2361C>A (p.Phe787Leu) c.645C>A (p.Phe215Leu) | |
| 2 | g.29222368A>C | CA346463043 | ALK | c.3491T>G (p.Phe1164Cys) c.718T>G n.368T>G c.287T>G (p.Phe96Cys) c.371T>G (p.Phe124Cys) c.185T>G (p.Phe62Cys) c.2360T>G (p.Phe787Cys) c.644T>G (p.Phe215Cys) | |
| 2 | g.29222368A>G | CA346463039 | ALK | c.3491T>C (p.Phe1164Ser) c.718T>C n.368T>C c.287T>C (p.Phe96Ser) c.371T>C (p.Phe124Ser) c.185T>C (p.Phe62Ser) c.2360T>C (p.Phe787Ser) c.644T>C (p.Phe215Ser) | |
| 2 | g.29222368A>T | CA346463045 | ALK | c.3491T>A (p.Phe1164Tyr) c.718T>A n.368T>A c.287T>A (p.Phe96Tyr) c.371T>A (p.Phe124Tyr) c.185T>A (p.Phe62Tyr) c.2360T>A (p.Phe787Tyr) c.644T>A (p.Phe215Tyr) | |
| 2 | g.29222369A>C | CA346463048 | ALK | c.3490T>G (p.Phe1164Val) c.717T>G n.367T>G c.286T>G (p.Phe96Val) c.370T>G (p.Phe124Val) c.184T>G (p.Phe62Val) c.2359T>G (p.Phe787Val) c.643T>G (p.Phe215Val) | |
| 2 | g.29222369A>G | CA346463051 | ALK | c.3490T>C (p.Phe1164Leu) c.717T>C n.367T>C c.286T>C (p.Phe96Leu) c.370T>C (p.Phe124Leu) c.184T>C (p.Phe62Leu) c.2359T>C (p.Phe787Leu) c.643T>C (p.Phe215Leu) | dbSNP |
| 2 | g.29222369A>T | CA346463055 | ALK | c.3490T>A (p.Phe1164Ile) c.717T>A n.367T>A c.286T>A (p.Phe96Ile) c.370T>A (p.Phe124Ile) c.184T>A (p.Phe62Ile) c.2359T>A (p.Phe787Ile) c.643T>A (p.Phe215Ile) | dbSNP |
| 2 | g.29222370A= | CA1241090516 | ALK | c.3489T= (p.Asp1163=) c.716T= n.366T= c.285T= (p.Asp95=) c.369T= (p.Asp123=) c.183T= (p.Asp61=) c.2358T= (p.Asp786=) c.642T= (p.Asp214=) | |
| 2 | g.29222370A>C | CA346463059 | ALK | c.3489T>G (p.Asp1163Glu) c.716T>G n.366T>G c.285T>G (p.Asp95Glu) c.369T>G (p.Asp123Glu) c.183T>G (p.Asp61Glu) c.2358T>G (p.Asp786Glu) c.642T>G (p.Asp214Glu) | |
| 2 | g.29222370A>G | CA425434570 | ALK | c.3489T>C (p.Asp1163=) c.716T>C n.366T>C c.285T>C (p.Asp95=) c.369T>C (p.Asp123=) c.183T>C (p.Asp61=) c.2358T>C (p.Asp786=) c.642T>C (p.Asp214=) | dbSNP |
| 2 | g.29222370A>T | CA346463061 | ALK | c.3489T>A (p.Asp1163Glu) c.716T>A n.366T>A c.285T>A (p.Asp95Glu) c.369T>A (p.Asp123Glu) c.183T>A (p.Asp61Glu) c.2358T>A (p.Asp786Glu) c.642T>A (p.Asp214Glu) | dbSNP |
| 2 | g.29222371T>A | CA346463063 | ALK | c.3488A>T (p.Asp1163Val) c.715A>T n.365A>T c.284A>T (p.Asp95Val) c.368A>T (p.Asp123Val) c.182A>T (p.Asp61Val) c.2357A>T (p.Asp786Val) c.641A>T (p.Asp214Val) | |
| 2 | g.29222371T>C | CA346463065 | ALK | c.3488A>G (p.Asp1163Gly) c.715A>G n.365A>G c.284A>G (p.Asp95Gly) c.368A>G (p.Asp123Gly) c.182A>G (p.Asp61Gly) c.2357A>G (p.Asp786Gly) c.641A>G (p.Asp214Gly) | |
| 2 | g.29222371T>G | CA346463067 | ALK | c.3488A>C (p.Asp1163Ala) c.715A>C n.365A>C c.284A>C (p.Asp95Ala) c.368A>C (p.Asp123Ala) c.182A>C (p.Asp61Ala) c.2357A>C (p.Asp786Ala) c.641A>C (p.Asp214Ala) | |
| 2 | g.29222372C>A | CA346463072 | ALK | c.3487G>T (p.Asp1163Tyr) c.714G>T n.364G>T c.283G>T (p.Asp95Tyr) c.367G>T (p.Asp123Tyr) c.181G>T (p.Asp61Tyr) c.2356G>T (p.Asp786Tyr) c.640G>T (p.Asp214Tyr) | dbSNP |
| 2 | g.29222372C= | CA1241090517 | ALK | c.3487G= (p.Asp1163=) c.714G= n.364G= c.283G= (p.Asp95=) c.367G= (p.Asp123=) c.181G= (p.Asp61=) c.2356G= (p.Asp786=) c.640G= (p.Asp214=) | |
| 2 | g.29222372C>G | CA346463074 | ALK | c.3487G>C (p.Asp1163His) c.714G>C n.364G>C c.283G>C (p.Asp95His) c.367G>C (p.Asp123His) c.181G>C (p.Asp61His) c.2356G>C (p.Asp786His) c.640G>C (p.Asp214His) | ClinVar dbSNP |
| 2 | g.29222372C>T | CA1593922 | ALK | c.3487G>A (p.Asp1163Asn) c.714G>A n.364G>A c.283G>A (p.Asp95Asn) c.367G>A (p.Asp123Asn) c.181G>A (p.Asp61Asn) c.2356G>A (p.Asp786Asn) c.640G>A (p.Asp214Asn) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 2 | g.29222373C>A | CA425434573 | ALK | c.3486G>T (p.Leu1162=) c.713G>T n.363G>T c.282G>T (p.Leu94=) c.366G>T (p.Leu122=) c.180G>T (p.Leu60=) c.2355G>T (p.Leu785=) c.639G>T (p.Leu213=) | dbSNP |
| 2 | g.29222373C= | CA1241090518 | ALK | c.3486G= (p.Leu1162=) c.713G= n.363G= c.282G= (p.Leu94=) c.366G= (p.Leu122=) c.180G= (p.Leu60=) c.2355G= (p.Leu785=) c.639G= (p.Leu213=) | |
| 2 | g.29222373C>G | CA425434571 | ALK | c.3486G>C (p.Leu1162=) c.713G>C n.363G>C c.282G>C (p.Leu94=) c.366G>C (p.Leu122=) c.180G>C (p.Leu60=) c.2355G>C (p.Leu785=) c.639G>C (p.Leu213=) | ClinVar dbSNP |
| 2 | g.29222373C>T | CA425434572 | ALK | c.3486G>A (p.Leu1162=) c.713G>A n.363G>A c.282G>A (p.Leu94=) c.366G>A (p.Leu122=) c.180G>A (p.Leu60=) c.2355G>A (p.Leu785=) c.639G>A (p.Leu213=) | dbSNP |
| 2 | g.29222374A= | CA1241090519 | ALK | c.3485T= (p.Leu1162=) c.712T= n.362T= c.281T= (p.Leu94=) c.365T= (p.Leu122=) c.179T= (p.Leu60=) c.2354T= (p.Leu785=) c.638T= (p.Leu213=) | |
| 2 | g.29222374A>C | CA346463084 | ALK | c.3485T>G (p.Leu1162Arg) c.712T>G n.362T>G c.281T>G (p.Leu94Arg) c.365T>G (p.Leu122Arg) c.179T>G (p.Leu60Arg) c.2354T>G (p.Leu785Arg) c.638T>G (p.Leu213Arg) | |
| 2 | g.29222374A>G | CA1593923 | ALK | c.3485T>C (p.Leu1162Pro) c.712T>C n.362T>C c.281T>C (p.Leu94Pro) c.365T>C (p.Leu122Pro) c.179T>C (p.Leu60Pro) c.2354T>C (p.Leu785Pro) c.638T>C (p.Leu213Pro) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 2 | g.29222374A>T | CA346463078 | ALK | c.3485T>A (p.Leu1162Gln) c.712T>A n.362T>A c.281T>A (p.Leu94Gln) c.365T>A (p.Leu122Gln) c.179T>A (p.Leu60Gln) c.2354T>A (p.Leu785Gln) c.638T>A (p.Leu213Gln) | ClinVar dbSNP |
| 2 | g.29222375G>A | CA425434574 | ALK | c.3484C>T (p.Leu1162=) c.711C>T n.361C>T c.280C>T (p.Leu94=) c.364C>T (p.Leu122=) c.178C>T (p.Leu60=) c.2353C>T (p.Leu785=) c.637C>T (p.Leu213=) | ClinVar dbSNP gnomAD v4 |
| 2 | g.29222375G>C | CA346463088 | ALK | c.3484C>G (p.Leu1162Val) c.711C>G n.361C>G c.280C>G (p.Leu94Val) c.364C>G (p.Leu122Val) c.178C>G (p.Leu60Val) c.2353C>G (p.Leu785Val) c.637C>G (p.Leu213Val) | dbSNP |
| 2 | g.29222375G>T | CA346463090 | ALK | c.3484C>A (p.Leu1162Met) c.711C>A n.361C>A c.280C>A (p.Leu94Met) c.364C>A (p.Leu122Met) c.178C>A (p.Leu60Met) c.2353C>A (p.Leu785Met) c.637C>A (p.Leu213Met) | |
| 2 | g.29222376T>A | CA346463094 | ALK | c.3483A>T (p.Glu1161Asp) c.710A>T n.360A>T c.279A>T (p.Glu93Asp) c.363A>T (p.Glu121Asp) c.177A>T (p.Glu59Asp) c.2352A>T (p.Glu784Asp) c.636A>T (p.Glu212Asp) | dbSNP |
| 2 | g.29222376T>C | CA425434575 | ALK | c.3483A>G (p.Glu1161=) c.710A>G n.360A>G c.279A>G (p.Glu93=) c.363A>G (p.Glu121=) c.177A>G (p.Glu59=) c.2352A>G (p.Glu784=) c.636A>G (p.Glu212=) | gnomAD v4 |
| 2 | g.29222376T>G | CA346463096 | ALK | c.3483A>C (p.Glu1161Asp) c.710A>C n.360A>C c.279A>C (p.Glu93Asp) c.363A>C (p.Glu121Asp) c.177A>C (p.Glu59Asp) c.2352A>C (p.Glu784Asp) c.636A>C (p.Glu212Asp) | dbSNP |
| 2 | g.29222377T>A | CA346463099 | ALK | c.3482A>T (p.Glu1161Val) c.709A>T n.359A>T c.278A>T (p.Glu93Val) c.362A>T (p.Glu121Val) c.176A>T (p.Glu59Val) c.2351A>T (p.Glu784Val) c.635A>T (p.Glu212Val) | dbSNP |
| 2 | g.29222377T>C | CA346463102 | ALK | c.3482A>G (p.Glu1161Gly) c.709A>G n.359A>G c.278A>G (p.Glu93Gly) c.362A>G (p.Glu121Gly) c.176A>G (p.Glu59Gly) c.2351A>G (p.Glu784Gly) c.635A>G (p.Glu212Gly) | |
| 2 | g.29222377T>G | CA346463104 | ALK | c.3482A>C (p.Glu1161Ala) c.709A>C n.359A>C c.278A>C (p.Glu93Ala) c.362A>C (p.Glu121Ala) c.176A>C (p.Glu59Ala) c.2351A>C (p.Glu784Ala) c.635A>C (p.Glu212Ala) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 2 | g.29222377T= | CA1241090521 | ALK | c.3482A= (p.Glu1161=) c.709A= n.359A= c.278A= (p.Glu93=) c.362A= (p.Glu121=) c.176A= (p.Glu59=) c.2351A= (p.Glu784=) c.635A= (p.Glu212=) | |
| 2 | g.29222377_29222378delinsGT | CA658655647 | ALK | c.3481_3482delinsAC (p.Glu1161Thr) c.708_709delinsAC n.358_359delinsAC c.277_278delinsAC (p.Glu93Thr) c.361_362delinsAC (p.Glu121Thr) c.175_176delinsAC (p.Glu59Thr) c.2350_2351delinsAC (p.Glu784Thr) c.634_635delinsAC (p.Glu212Thr) | ClinVar dbSNP |
| 2 | g.29222377_29222378delinsTC | CA1241090520 | ALK | c.3481_3482delinsGA (p.Glu1161=) c.708_709delinsGA n.358_359delinsGA c.277_278delinsGA (p.Glu93=) c.361_362delinsGA (p.Glu121=) c.175_176delinsGA (p.Glu59=) c.2350_2351delinsGA (p.Glu784=) c.634_635delinsGA (p.Glu212=) | |
| 2 | g.29222378C>A | CA346463107 | ALK | c.3481G>T (p.Glu1161Ter) c.708G>T n.358G>T c.277G>T (p.Glu93Ter) c.361G>T (p.Glu121Ter) c.175G>T (p.Glu59Ter) c.2350G>T (p.Glu784Ter) c.634G>T (p.Glu212Ter) | dbSNP |
| 2 | g.29222378C= | CA1241090522 | ALK | c.3481G= (p.Glu1161=) c.708G= n.358G= c.277G= (p.Glu93=) c.361G= (p.Glu121=) c.175G= (p.Glu59=) c.2350G= (p.Glu784=) c.634G= (p.Glu212=) | |
| 2 | g.29222378C>G | CA346463121 | ALK | c.3481G>C (p.Glu1161Gln) c.708G>C n.358G>C c.277G>C (p.Glu93Gln) c.361G>C (p.Glu121Gln) c.175G>C (p.Glu59Gln) c.2350G>C (p.Glu784Gln) c.634G>C (p.Glu212Gln) | dbSNP |
| 2 | g.29222378C>T | CA1593924 | ALK | c.3481G>A (p.Glu1161Lys) c.708G>A n.358G>A c.277G>A (p.Glu93Lys) c.361G>A (p.Glu121Lys) c.175G>A (p.Glu59Lys) c.2350G>A (p.Glu784Lys) c.634G>A (p.Glu212Lys) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 2 | g.29222379G>A | CA44631202 | ALK | c.3480C>T (p.Asp1160=) c.707C>T n.357C>T c.276C>T (p.Asp92=) c.360C>T (p.Asp120=) c.174C>T (p.Asp58=) c.2349C>T (p.Asp783=) c.633C>T (p.Asp211=) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 2 | g.29222379G>C | CA346463127 | ALK | c.3480C>G (p.Asp1160Glu) c.707C>G n.357C>G c.276C>G (p.Asp92Glu) c.360C>G (p.Asp120Glu) c.174C>G (p.Asp58Glu) c.2349C>G (p.Asp783Glu) c.633C>G (p.Asp211Glu) | dbSNP |
| 2 | g.29222379G= | CA1241090523 | ALK | c.3480C= (p.Asp1160=) c.707C= n.357C= c.276C= (p.Asp92=) c.360C= (p.Asp120=) c.174C= (p.Asp58=) c.2349C= (p.Asp783=) c.633C= (p.Asp211=) | |
| 2 | g.29222379G>T | CA346463129 | ALK | c.3480C>A (p.Asp1160Glu) c.707C>A n.357C>A c.276C>A (p.Asp92Glu) c.360C>A (p.Asp120Glu) c.174C>A (p.Asp58Glu) c.2349C>A (p.Asp783Glu) c.633C>A (p.Asp211Glu) | dbSNP |
| 2 | g.29222380T>A | CA346463136 | ALK | c.3479A>T (p.Asp1160Val) c.706A>T n.356A>T c.275A>T (p.Asp92Val) c.359A>T (p.Asp120Val) c.173A>T (p.Asp58Val) c.2348A>T (p.Asp783Val) c.632A>T (p.Asp211Val) | dbSNP |
| 2 | g.29222380T>C | CA346463157 | ALK | c.3479A>G (p.Asp1160Gly) c.706A>G n.356A>G c.275A>G (p.Asp92Gly) c.359A>G (p.Asp120Gly) c.173A>G (p.Asp58Gly) c.2348A>G (p.Asp783Gly) c.632A>G (p.Asp211Gly) | ClinVar dbSNP gnomAD v4 |
| 2 | g.29222380T>G | CA346463132 | ALK | c.3479A>C (p.Asp1160Ala) c.706A>C n.356A>C c.275A>C (p.Asp92Ala) c.359A>C (p.Asp120Ala) c.173A>C (p.Asp58Ala) c.2348A>C (p.Asp783Ala) c.632A>C (p.Asp211Ala) | |
| 2 | g.29222381C>A | CA346463163 | ALK | c.3478G>T (p.Asp1160Tyr) c.705G>T n.355G>T c.274G>T (p.Asp92Tyr) c.358G>T (p.Asp120Tyr) c.172G>T (p.Asp58Tyr) c.2347G>T (p.Asp783Tyr) c.631G>T (p.Asp211Tyr) | dbSNP |
| 2 | g.29222381C>G | CA346463164 | ALK | c.3478G>C (p.Asp1160His) c.705G>C n.355G>C c.274G>C (p.Asp92His) c.358G>C (p.Asp120His) c.172G>C (p.Asp58His) c.2347G>C (p.Asp783His) c.631G>C (p.Asp211His) | dbSNP |
| 2 | g.29222381C>T | CA346463167 | ALK | c.3478G>A (p.Asp1160Asn) c.705G>A n.355G>A c.274G>A (p.Asp92Asn) c.358G>A (p.Asp120Asn) c.172G>A (p.Asp58Asn) c.2347G>A (p.Asp783Asn) c.631G>A (p.Asp211Asn) | dbSNP |
| 2 | g.29222382C>A | CA346463168 | ALK | c.3477G>T (p.Gln1159His) c.704G>T n.354G>T c.273G>T (p.Gln91His) c.357G>T (p.Gln119His) c.171G>T (p.Gln57His) c.2346G>T (p.Gln782His) c.630G>T (p.Gln210His) | dbSNP |
| 2 | g.29222382C>G | CA346463169 | ALK | c.3477G>C (p.Gln1159His) c.704G>C n.354G>C c.273G>C (p.Gln91His) c.357G>C (p.Gln119His) c.171G>C (p.Gln57His) c.2346G>C (p.Gln782His) c.630G>C (p.Gln210His) | |
| 2 | g.29222382C>T | CA425434579 | ALK | c.3477G>A (p.Gln1159=) c.704G>A n.354G>A c.273G>A (p.Gln91=) c.357G>A (p.Gln119=) c.171G>A (p.Gln57=) c.2346G>A (p.Gln782=) c.630G>A (p.Gln210=) | dbSNP |
| 2 | g.29222383T>A | CA346463174 | ALK | c.3476A>T (p.Gln1159Leu) c.703A>T n.353A>T c.272A>T (p.Gln91Leu) c.356A>T (p.Gln119Leu) c.170A>T (p.Gln57Leu) c.2345A>T (p.Gln782Leu) c.629A>T (p.Gln210Leu) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 2 | g.29222383T>C | CA346463178 | ALK | c.3476A>G (p.Gln1159Arg) c.703A>G n.353A>G c.272A>G (p.Gln91Arg) c.356A>G (p.Gln119Arg) c.170A>G (p.Gln57Arg) c.2345A>G (p.Gln782Arg) c.629A>G (p.Gln210Arg) | dbSNP |
| 2 | g.29222383T>G | CA346463179 | ALK | c.3476A>C (p.Gln1159Pro) c.703A>C n.353A>C c.272A>C (p.Gln91Pro) c.356A>C (p.Gln119Pro) c.170A>C (p.Gln57Pro) c.2345A>C (p.Gln782Pro) c.629A>C (p.Gln210Pro) | |
| 2 | g.29222383T= | CA1241090524 | ALK | c.3476A= (p.Gln1159=) c.703A= n.353A= c.272A= (p.Gln91=) c.356A= (p.Gln119=) c.170A= (p.Gln57=) c.2345A= (p.Gln782=) c.629A= (p.Gln210=) | |
| 2 | g.29222384G>A | CA346463181 | ALK | c.3475C>T (p.Gln1159Ter) c.702C>T n.352C>T c.271C>T (p.Gln91Ter) c.355C>T (p.Gln119Ter) c.169C>T (p.Gln57Ter) c.2344C>T (p.Gln782Ter) c.628C>T (p.Gln210Ter) | dbSNP |
| 2 | g.29222384G>C | CA346463184 | ALK | c.3475C>G (p.Gln1159Glu) c.702C>G n.352C>G c.271C>G (p.Gln91Glu) c.355C>G (p.Gln119Glu) c.169C>G (p.Gln57Glu) c.2344C>G (p.Gln782Glu) c.628C>G (p.Gln210Glu) | dbSNP |
| 2 | g.29222384G>T | CA346463188 | ALK | c.3475C>A (p.Gln1159Lys) c.702C>A n.352C>A c.271C>A (p.Gln91Lys) c.355C>A (p.Gln119Lys) c.169C>A (p.Gln57Lys) c.2344C>A (p.Gln782Lys) c.628C>A (p.Gln210Lys) | dbSNP |
| 2 | g.29222385T>A | CA346463190 | ALK | c.3474A>T (p.Glu1158Asp) c.701A>T n.351A>T c.270A>T (p.Glu90Asp) c.354A>T (p.Glu118Asp) c.168A>T (p.Glu56Asp) c.2343A>T (p.Glu781Asp) c.627A>T (p.Glu209Asp) | dbSNP |
| 2 | g.29222385T>C | CA425434580 | ALK | c.3474A>G (p.Glu1158=) c.701A>G n.351A>G c.270A>G (p.Glu90=) c.354A>G (p.Glu118=) c.168A>G (p.Glu56=) c.2343A>G (p.Glu781=) c.627A>G (p.Glu209=) | dbSNP |
| 2 | g.29222385T>G | CA346463191 | ALK | c.3474A>C (p.Glu1158Asp) c.701A>C n.351A>C c.270A>C (p.Glu90Asp) c.354A>C (p.Glu118Asp) c.168A>C (p.Glu56Asp) c.2343A>C (p.Glu781Asp) c.627A>C (p.Glu209Asp) | dbSNP |
| 2 | g.29222385T= | CA1241090525 | ALK | c.3474A= (p.Glu1158=) c.701A= n.351A= c.270A= (p.Glu90=) c.354A= (p.Glu118=) c.168A= (p.Glu56=) c.2343A= (p.Glu781=) c.627A= (p.Glu209=) | |
| 2 | g.29222386T>A | CA346463198 | ALK | c.3473A>T (p.Glu1158Val) c.700A>T n.350A>T c.269A>T (p.Glu90Val) c.353A>T (p.Glu118Val) c.167A>T (p.Glu56Val) c.2342A>T (p.Glu781Val) c.626A>T (p.Glu209Val) | |
| 2 | g.29222386T>C | CA346463196 | ALK | c.3473A>G (p.Glu1158Gly) c.700A>G n.350A>G c.269A>G (p.Glu90Gly) c.353A>G (p.Glu118Gly) c.167A>G (p.Glu56Gly) c.2342A>G (p.Glu781Gly) c.626A>G (p.Glu209Gly) | dbSNP |
| 2 | g.29222386T>G | CA346463194 | ALK | c.3473A>C (p.Glu1158Ala) c.700A>C n.350A>C c.269A>C (p.Glu90Ala) c.353A>C (p.Glu118Ala) c.167A>C (p.Glu56Ala) c.2342A>C (p.Glu781Ala) c.626A>C (p.Glu209Ala) | |
| 2 | g.29222387C>A | CA346463200 | ALK | c.3472G>T (p.Glu1158Ter) c.699G>T n.349G>T c.268G>T (p.Glu90Ter) c.352G>T (p.Glu118Ter) c.166G>T (p.Glu56Ter) c.2341G>T (p.Glu781Ter) c.625G>T (p.Glu209Ter) | dbSNP |
| 2 | g.29222387C= | CA1241090526 | ALK | c.3472G= (p.Glu1158=) c.699G= n.349G= c.268G= (p.Glu90=) c.352G= (p.Glu118=) c.166G= (p.Glu56=) c.2341G= (p.Glu781=) c.625G= (p.Glu209=) | |
| 2 | g.29222387C>G | CA1593925 | ALK | c.3472G>C (p.Glu1158Gln) c.699G>C n.349G>C c.268G>C (p.Glu90Gln) c.352G>C (p.Glu118Gln) c.166G>C (p.Glu56Gln) c.2341G>C (p.Glu781Gln) c.625G>C (p.Glu209Gln) | dbSNP ExAC gnomAD v2 |
| 2 | g.29222387C>T | CA346463205 | ALK | c.3472G>A (p.Glu1158Lys) c.699G>A n.349G>A c.268G>A (p.Glu90Lys) c.352G>A (p.Glu118Lys) c.166G>A (p.Glu56Lys) c.2341G>A (p.Glu781Lys) c.625G>A (p.Glu209Lys) | ClinVar dbSNP |
| 2 | g.29222388A= | CA1241090527 | ALK | c.3471T= (p.Ser1157=) c.698T= n.348T= c.267T= (p.Ser89=) c.351T= (p.Ser117=) c.165T= (p.Ser55=) c.2340T= (p.Ser780=) c.624T= (p.Ser208=) | |
| 2 | g.29222388A>C | CA1593926 | ALK | c.3471T>G (p.Ser1157=) c.698T>G n.348T>G c.267T>G (p.Ser89=) c.351T>G (p.Ser117=) c.165T>G (p.Ser55=) c.2340T>G (p.Ser780=) c.624T>G (p.Ser208=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 2 | g.29222388A>G | CA425434581 | ALK | c.3471T>C (p.Ser1157=) c.698T>C n.348T>C c.267T>C (p.Ser89=) c.351T>C (p.Ser117=) c.165T>C (p.Ser55=) c.2340T>C (p.Ser780=) c.624T>C (p.Ser208=) | ClinVar dbSNP gnomAD v4 |
| 2 | g.29222388A>T | CA425434582 | ALK | c.3471T>A (p.Ser1157=) c.698T>A n.348T>A c.267T>A (p.Ser89=) c.351T>A (p.Ser117=) c.165T>A (p.Ser55=) c.2340T>A (p.Ser780=) c.624T>A (p.Ser208=) | dbSNP |
| 2 | g.29222389G>A | CA346463209 | ALK | c.3470C>T (p.Ser1157Phe) c.697C>T n.347C>T c.266C>T (p.Ser89Phe) c.350C>T (p.Ser117Phe) c.164C>T (p.Ser55Phe) c.2339C>T (p.Ser780Phe) c.623C>T (p.Ser208Phe) | dbSNP |
| 2 | g.29222389G>C | CA346463210 | ALK | c.3470C>G (p.Ser1157Cys) c.697C>G n.347C>G c.266C>G (p.Ser89Cys) c.350C>G (p.Ser117Cys) c.164C>G (p.Ser55Cys) c.2339C>G (p.Ser780Cys) c.623C>G (p.Ser208Cys) | dbSNP |
| 2 | g.29222389G>T | CA346463211 | ALK | c.3470C>A (p.Ser1157Tyr) c.697C>A n.347C>A c.266C>A (p.Ser89Tyr) c.350C>A (p.Ser117Tyr) c.164C>A (p.Ser55Tyr) c.2339C>A (p.Ser780Tyr) c.623C>A (p.Ser208Tyr) | |
| 2 | g.29222390A= | CA1241090528 | ALK | c.3469T= (p.Ser1157=) c.696T= n.346T= c.265T= (p.Ser89=) c.349T= (p.Ser117=) c.163T= (p.Ser55=) c.2338T= (p.Ser780=) c.622T= (p.Ser208=) | |
| 2 | g.29222390A>C | CA346463214 | ALK | c.3469T>G (p.Ser1157Ala) c.696T>G n.346T>G c.265T>G (p.Ser89Ala) c.349T>G (p.Ser117Ala) c.163T>G (p.Ser55Ala) c.2338T>G (p.Ser780Ala) c.622T>G (p.Ser208Ala) | |
| 2 | g.29222390A>G | CA346463218 | ALK | c.3469T>C (p.Ser1157Pro) c.696T>C n.346T>C c.265T>C (p.Ser89Pro) c.349T>C (p.Ser117Pro) c.163T>C (p.Ser55Pro) c.2338T>C (p.Ser780Pro) c.622T>C (p.Ser208Pro) | ClinVar dbSNP |
| 2 | g.29222390A>T | CA346463224 | ALK | c.3469T>A (p.Ser1157Thr) c.696T>A n.346T>A c.265T>A (p.Ser89Thr) c.349T>A (p.Ser117Thr) c.163T>A (p.Ser55Thr) c.2338T>A (p.Ser780Thr) c.622T>A (p.Ser208Thr) | dbSNP COSMIC |
| 2 | g.29222391G>A | CA425434583 | ALK | c.3468C>T (p.Cys1156=) c.695C>T n.345C>T c.264C>T (p.Cys88=) c.348C>T (p.Cys116=) c.162C>T (p.Cys54=) c.2337C>T (p.Cys779=) c.621C>T (p.Cys207=) | dbSNP |
| 2 | g.29222391G>C | CA346463229 | ALK | c.3468C>G (p.Cys1156Trp) c.695C>G n.345C>G c.264C>G (p.Cys88Trp) c.348C>G (p.Cys116Trp) c.162C>G (p.Cys54Trp) c.2337C>G (p.Cys779Trp) c.621C>G (p.Cys207Trp) | dbSNP |
| 2 | g.29222391G>T | CA346463231 | ALK | c.3468C>A (p.Cys1156Ter) c.695C>A n.345C>A c.264C>A (p.Cys88Ter) c.348C>A (p.Cys116Ter) c.162C>A (p.Cys54Ter) c.2337C>A (p.Cys779Ter) c.621C>A (p.Cys207Ter) | |
| 2 | g.29222392C>A | CA346463242 | ALK | c.3467G>T (p.Cys1156Phe) c.694G>T n.344G>T c.263G>T (p.Cys88Phe) c.347G>T (p.Cys116Phe) c.161G>T (p.Cys54Phe) c.2336G>T (p.Cys779Phe) c.620G>T (p.Cys207Phe) | dbSNP |
| 2 | g.29222392C= | CA1241090529 | ALK | c.3467G= (p.Cys1156=) c.694G= n.344G= c.263G= (p.Cys88=) c.347G= (p.Cys116=) c.161G= (p.Cys54=) c.2336G= (p.Cys779=) c.620G= (p.Cys207=) | |
| 2 | g.29222392C>G | CA346463239 | ALK | c.3467G>C (p.Cys1156Ser) c.694G>C n.344G>C c.263G>C (p.Cys88Ser) c.347G>C (p.Cys116Ser) c.161G>C (p.Cys54Ser) c.2336G>C (p.Cys779Ser) c.620G>C (p.Cys207Ser) | dbSNP |
| 2 | g.29222392C>T | CA16602783 | ALK | c.3467G>A (p.Cys1156Tyr) c.694G>A n.344G>A c.263G>A (p.Cys88Tyr) c.347G>A (p.Cys116Tyr) c.161G>A (p.Cys54Tyr) c.2336G>A (p.Cys779Tyr) c.620G>A (p.Cys207Tyr) | ClinVar dbSNP COSMIC |
| 2 | g.29222393A>C | CA346463245 | ALK | c.3466T>G (p.Cys1156Gly) c.693T>G n.343T>G c.262T>G (p.Cys88Gly) c.346T>G (p.Cys116Gly) c.160T>G (p.Cys54Gly) c.2335T>G (p.Cys779Gly) c.619T>G (p.Cys207Gly) | ClinVar |
| 2 | g.29222393A>G | CA346463248 | ALK | c.3466T>C (p.Cys1156Arg) c.693T>C n.343T>C c.262T>C (p.Cys88Arg) c.346T>C (p.Cys116Arg) c.160T>C (p.Cys54Arg) c.2335T>C (p.Cys779Arg) c.619T>C (p.Cys207Arg) | ClinVar dbSNP |
| 2 | g.29222393A>T | CA346463247 | ALK | c.3466T>A (p.Cys1156Ser) c.693T>A n.343T>A c.262T>A (p.Cys88Ser) c.346T>A (p.Cys116Ser) c.160T>A (p.Cys54Ser) c.2335T>A (p.Cys779Ser) c.619T>A (p.Cys207Ser) | |
| 2 | g.29222394C>A | CA425434586 | ALK | c.3465G>T (p.Val1155=) c.692G>T n.342G>T c.261G>T (p.Val87=) c.345G>T (p.Val115=) c.159G>T (p.Val53=) c.2334G>T (p.Val778=) c.618G>T (p.Val206=) | |
| 2 | g.29222394C>G | CA425434584 | ALK | c.3465G>C (p.Val1155=) c.692G>C n.342G>C c.261G>C (p.Val87=) c.345G>C (p.Val115=) c.159G>C (p.Val53=) c.2334G>C (p.Val778=) c.618G>C (p.Val206=) | dbSNP |
| 2 | g.29222394C>T | CA425434585 | ALK | c.3465G>A (p.Val1155=) c.692G>A n.342G>A c.261G>A (p.Val87=) c.345G>A (p.Val115=) c.159G>A (p.Val53=) c.2334G>A (p.Val778=) c.618G>A (p.Val206=) | ClinVar dbSNP |
| 2 | g.29222395A= | CA1241090530 | ALK | c.3464T= (p.Val1155=) c.691T= n.341T= c.260T= (p.Val87=) c.344T= (p.Val115=) c.158T= (p.Val53=) c.2333T= (p.Val778=) c.617T= (p.Val206=) | |
| 2 | g.29222395A>C | CA346463250 | ALK | c.3464T>G (p.Val1155Gly) c.691T>G n.341T>G c.260T>G (p.Val87Gly) c.344T>G (p.Val115Gly) c.158T>G (p.Val53Gly) c.2333T>G (p.Val778Gly) c.617T>G (p.Val206Gly) | dbSNP |
| 2 | g.29222395A>G | CA346463253 | ALK | c.3464T>C (p.Val1155Ala) c.691T>C n.341T>C c.260T>C (p.Val87Ala) c.344T>C (p.Val115Ala) c.158T>C (p.Val53Ala) c.2333T>C (p.Val778Ala) c.617T>C (p.Val206Ala) | ClinVar dbSNP gnomAD v4 |
| 2 | g.29222395A>T | CA346463257 | ALK | c.3464T>A (p.Val1155Glu) c.691T>A n.341T>A c.260T>A (p.Val87Glu) c.344T>A (p.Val115Glu) c.158T>A (p.Val53Glu) c.2333T>A (p.Val778Glu) c.617T>A (p.Val206Glu) | dbSNP |
| 2 | g.29222396C>A | CA346463262 | ALK | c.3463G>T (p.Val1155Leu) c.690G>T n.340G>T c.259G>T (p.Val87Leu) c.343G>T (p.Val115Leu) c.157G>T (p.Val53Leu) c.2332G>T (p.Val778Leu) c.616G>T (p.Val206Leu) | dbSNP |
| 2 | g.29222396C= | CA1241090531 | ALK | c.3463G= (p.Val1155=) c.690G= n.340G= c.259G= (p.Val87=) c.343G= (p.Val115=) c.157G= (p.Val53=) c.2332G= (p.Val778=) c.616G= (p.Val206=) | |
| 2 | g.29222396C>G | CA346463264 | ALK | c.3463G>C (p.Val1155Leu) c.690G>C n.340G>C c.259G>C (p.Val87Leu) c.343G>C (p.Val115Leu) c.157G>C (p.Val53Leu) c.2332G>C (p.Val778Leu) c.616G>C (p.Val206Leu) | dbSNP |
| 2 | g.29222396C>T | CA44631223 | ALK | c.3463G>A (p.Val1155Met) c.690G>A n.340G>A c.259G>A (p.Val87Met) c.343G>A (p.Val115Met) c.157G>A (p.Val53Met) c.2332G>A (p.Val778Met) c.616G>A (p.Val206Met) | dbSNP gnomAD v4 |
| 2 | g.29222397T>A | CA346463266 | ALK | c.3462A>T (p.Glu1154Asp) c.689A>T n.339A>T c.258A>T (p.Glu86Asp) c.342A>T (p.Glu114Asp) c.156A>T (p.Glu52Asp) c.2331A>T (p.Glu777Asp) c.615A>T (p.Glu205Asp) | |
| 2 | g.29222397T>C | CA425434587 | ALK | c.3462A>G (p.Glu1154=) c.689A>G n.339A>G c.258A>G (p.Glu86=) c.342A>G (p.Glu114=) c.156A>G (p.Glu52=) c.2331A>G (p.Glu777=) c.615A>G (p.Glu205=) | |
| 2 | g.29222397T>G | CA346463269 | ALK | c.3462A>C (p.Glu1154Asp) c.689A>C n.339A>C c.258A>C (p.Glu86Asp) c.342A>C (p.Glu114Asp) c.156A>C (p.Glu52Asp) c.2331A>C (p.Glu777Asp) c.615A>C (p.Glu205Asp) | |
| 2 | g.29222398T>A | CA346463271 | ALK | c.3461A>T (p.Glu1154Val) c.688A>T n.338A>T c.257A>T (p.Glu86Val) c.341A>T (p.Glu114Val) c.155A>T (p.Glu52Val) c.2330A>T (p.Glu777Val) c.614A>T (p.Glu205Val) | dbSNP |
| 2 | g.29222398T>C | CA346463274 | ALK | c.3461A>G (p.Glu1154Gly) c.688A>G n.338A>G c.257A>G (p.Glu86Gly) c.341A>G (p.Glu114Gly) c.155A>G (p.Glu52Gly) c.2330A>G (p.Glu777Gly) c.614A>G (p.Glu205Gly) | dbSNP |
| 2 | g.29222398T>G | CA346463287 | ALK | c.3461A>C (p.Glu1154Ala) c.688A>C n.338A>C c.257A>C (p.Glu86Ala) c.341A>C (p.Glu114Ala) c.155A>C (p.Glu52Ala) c.2330A>C (p.Glu777Ala) c.614A>C (p.Glu205Ala) | ClinVar dbSNP gnomAD v4 |
| 2 | g.29222398T= | CA1241090532 | ALK | c.3461A= (p.Glu1154=) c.688A= n.338A= c.257A= (p.Glu86=) c.341A= (p.Glu114=) c.155A= (p.Glu52=) c.2330A= (p.Glu777=) c.614A= (p.Glu205=) | |
| 2 | g.29222399C>A | CA346463294 | ALK | c.3460G>T (p.Glu1154Ter) c.687G>T n.337G>T c.256G>T (p.Glu86Ter) c.340G>T (p.Glu114Ter) c.154G>T (p.Glu52Ter) c.2329G>T (p.Glu777Ter) c.613G>T (p.Glu205Ter) | dbSNP |
| 2 | g.29222399C= | CA1241090533 | ALK | c.3460G= (p.Glu1154=) c.687G= n.337G= c.256G= (p.Glu86=) c.340G= (p.Glu114=) c.154G= (p.Glu52=) c.2329G= (p.Glu777=) c.613G= (p.Glu205=) | |
| 2 | g.29222399C>G | CA44631230 | ALK | c.3460G>C (p.Glu1154Gln) c.687G>C n.337G>C c.256G>C (p.Glu86Gln) c.340G>C (p.Glu114Gln) c.154G>C (p.Glu52Gln) c.2329G>C (p.Glu777Gln) c.613G>C (p.Glu205Gln) | ClinVar dbSNP gnomAD v4 |
| 2 | g.29222399C>T | CA346463289 | ALK | c.3460G>A (p.Glu1154Lys) c.687G>A n.337G>A c.256G>A (p.Glu86Lys) c.340G>A (p.Glu114Lys) c.154G>A (p.Glu52Lys) c.2329G>A (p.Glu777Lys) c.613G>A (p.Glu205Lys) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 2 | g.29222400A= | CA1241090534 | ALK | c.3459T= (p.Pro1153=) c.686T= n.336T= c.255T= (p.Pro85=) c.339T= (p.Pro113=) c.153T= (p.Pro51=) c.2328T= (p.Pro776=) c.612T= (p.Pro204=) | |
| 2 | g.29222400A>C | CA425434589 | ALK | c.3459T>G (p.Pro1153=) c.686T>G n.336T>G c.255T>G (p.Pro85=) c.339T>G (p.Pro113=) c.153T>G (p.Pro51=) c.2328T>G (p.Pro776=) c.612T>G (p.Pro204=) | |
| 2 | g.29222400A>G | CA425434588 | ALK | c.3459T>C (p.Pro1153=) c.686T>C n.336T>C c.255T>C (p.Pro85=) c.339T>C (p.Pro113=) c.153T>C (p.Pro51=) c.2328T>C (p.Pro776=) c.612T>C (p.Pro204=) | dbSNP |
| 2 | g.29222400A>T | CA425434590 | ALK | c.3459T>A (p.Pro1153=) c.686T>A n.336T>A c.255T>A (p.Pro85=) c.339T>A (p.Pro113=) c.153T>A (p.Pro51=) c.2328T>A (p.Pro776=) c.612T>A (p.Pro204=) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 2 | g.29222401G>A | CA346463303 | ALK | c.3458C>T (p.Pro1153Leu) c.685C>T n.335C>T c.254C>T (p.Pro85Leu) c.338C>T (p.Pro113Leu) c.152C>T (p.Pro51Leu) c.2327C>T (p.Pro776Leu) c.611C>T (p.Pro204Leu) | dbSNP |
| 2 | g.29222401G>C | CA44631234 | ALK | c.3458C>G (p.Pro1153Arg) c.685C>G n.335C>G c.254C>G (p.Pro85Arg) c.338C>G (p.Pro113Arg) c.152C>G (p.Pro51Arg) c.2327C>G (p.Pro776Arg) c.611C>G (p.Pro204Arg) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 2 | g.29222401G= | CA1241090535 | ALK | c.3458C= (p.Pro1153=) c.685C= n.335C= c.254C= (p.Pro85=) c.338C= (p.Pro113=) c.152C= (p.Pro51=) c.2327C= (p.Pro776=) c.611C= (p.Pro204=) | |
| 2 | g.29222401G>T | CA346463309 | ALK | c.3458C>A (p.Pro1153His) c.685C>A n.335C>A c.254C>A (p.Pro85His) c.338C>A (p.Pro113His) c.152C>A (p.Pro51His) c.2327C>A (p.Pro776His) c.611C>A (p.Pro204His) | dbSNP |
| 2 | g.29222402G>A | CA346463314 | ALK | c.3457C>T (p.Pro1153Ser) c.684C>T n.334C>T c.253C>T (p.Pro85Ser) c.337C>T (p.Pro113Ser) c.151C>T (p.Pro51Ser) c.2326C>T (p.Pro776Ser) c.610C>T (p.Pro204Ser) | dbSNP |
| 2 | g.29222402G>C | CA346463317 | ALK | c.3457C>G (p.Pro1153Ala) c.684C>G n.334C>G c.253C>G (p.Pro85Ala) c.337C>G (p.Pro113Ala) c.151C>G (p.Pro51Ala) c.2326C>G (p.Pro776Ala) c.610C>G (p.Pro204Ala) | dbSNP |
| 2 | g.29222402G>T | CA346463322 | ALK | c.3457C>A (p.Pro1153Thr) c.684C>A n.334C>A c.253C>A (p.Pro85Thr) c.337C>A (p.Pro113Thr) c.151C>A (p.Pro51Thr) c.2326C>A (p.Pro776Thr) c.610C>A (p.Pro204Thr) | dbSNP |
| 2 | g.29222403C>A | CA425434592 | ALK | c.3456G>T (p.Leu1152=) c.683G>T n.333G>T c.252G>T (p.Leu84=) c.336G>T (p.Leu112=) c.150G>T (p.Leu50=) c.2325G>T (p.Leu775=) c.609G>T (p.Leu203=) | dbSNP |
| 2 | g.29222403C>G | CA425434593 | ALK | c.3456G>C (p.Leu1152=) c.683G>C n.333G>C c.252G>C (p.Leu84=) c.336G>C (p.Leu112=) c.150G>C (p.Leu50=) c.2325G>C (p.Leu775=) c.609G>C (p.Leu203=) | dbSNP |
| 2 | g.29222403C>T | CA425434594 | ALK | c.3456G>A (p.Leu1152=) c.683G>A n.333G>A c.252G>A (p.Leu84=) c.336G>A (p.Leu112=) c.150G>A (p.Leu50=) c.2325G>A (p.Leu775=) c.609G>A (p.Leu203=) | dbSNP gnomAD v4 |
| 2 | g.29222404A= | CA1241090536 | ALK | c.3455T= (p.Leu1152=) c.682T= n.332T= c.251T= (p.Leu84=) c.335T= (p.Leu112=) c.149T= (p.Leu50=) c.2324T= (p.Leu775=) c.608T= (p.Leu203=) | |
| 2 | g.29222404A>C | CA16602594 | ALK | c.3455T>G (p.Leu1152Arg) c.682T>G n.332T>G c.251T>G (p.Leu84Arg) c.335T>G (p.Leu112Arg) c.149T>G (p.Leu50Arg) c.2324T>G (p.Leu775Arg) c.608T>G (p.Leu203Arg) | ClinVar dbSNP COSMIC |
| 2 | g.29222404A>G | CA346463323 | ALK | c.3455T>C (p.Leu1152Pro) c.682T>C n.332T>C c.251T>C (p.Leu84Pro) c.335T>C (p.Leu112Pro) c.149T>C (p.Leu50Pro) c.2324T>C (p.Leu775Pro) c.608T>C (p.Leu203Pro) | dbSNP |
| 2 | g.29222404A>T | CA346463324 | ALK | c.3455T>A (p.Leu1152Gln) c.682T>A n.332T>A c.251T>A (p.Leu84Gln) c.335T>A (p.Leu112Gln) c.149T>A (p.Leu50Gln) c.2324T>A (p.Leu775Gln) c.608T>A (p.Leu203Gln) | dbSNP |
| 2 | g.29222405G>A | CA425434596 | ALK | c.3454C>T (p.Leu1152=) c.681C>T n.331C>T c.250C>T (p.Leu84=) c.334C>T (p.Leu112=) c.148C>T (p.Leu50=) c.2323C>T (p.Leu775=) c.607C>T (p.Leu203=) | dbSNP gnomAD v4 |
| 2 | g.29222405G>C | CA346463325 | ALK | c.3454C>G (p.Leu1152Val) c.681C>G n.331C>G c.250C>G (p.Leu84Val) c.334C>G (p.Leu112Val) c.148C>G (p.Leu50Val) c.2323C>G (p.Leu775Val) c.607C>G (p.Leu203Val) | |
| 2 | g.29222405G>T | CA346463344 | ALK | c.3454C>A (p.Leu1152Met) c.681C>A n.331C>A c.250C>A (p.Leu84Met) c.334C>A (p.Leu112Met) c.148C>A (p.Leu50Met) c.2323C>A (p.Leu775Met) c.607C>A (p.Leu203Met) | |
| 2 | g.29222406C>A | CA425434599 | ALK | c.3453G>T (p.Thr1151=) c.680G>T n.330G>T c.249G>T (p.Thr83=) c.333G>T (p.Thr111=) c.147G>T (p.Thr49=) c.2322G>T (p.Thr774=) c.606G>T (p.Thr202=) | dbSNP |
| 2 | g.29222406C= | CA1241090537 | ALK | c.3453G= (p.Thr1151=) c.680G= n.330G= c.249G= (p.Thr83=) c.333G= (p.Thr111=) c.147G= (p.Thr49=) c.2322G= (p.Thr774=) c.606G= (p.Thr202=) | |
| 2 | g.29222406C>G | CA425434601 | ALK | c.3453G>C (p.Thr1151=) c.680G>C n.330G>C c.249G>C (p.Thr83=) c.333G>C (p.Thr111=) c.147G>C (p.Thr49=) c.2322G>C (p.Thr774=) c.606G>C (p.Thr202=) | dbSNP |
| 2 | g.29222406C>T | CA1593927 | ALK | c.3453G>A (p.Thr1151=) c.680G>A n.330G>A c.249G>A (p.Thr83=) c.333G>A (p.Thr111=) c.147G>A (p.Thr49=) c.2322G>A (p.Thr774=) c.606G>A (p.Thr202=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 2 | g.29222407_29222409dup | CA645528802 | ALK | c.3451_3453dup c.678_680dup n.328_330dup c.247_249dup c.331_333dup c.145_147dup c.2320_2322dup c.604_606dup | dbSNP COSMIC |
| 2 | g.29222407del | CA2658458347 | ALK | c.3452del (p.Thr1151SerfsTer19) c.679del n.329del c.248del (p.Thr83SerfsTer19) c.332del (p.Thr111SerfsTer19) c.146del (p.Thr49SerfsTer19) c.2321del (p.Thr774SerfsTer19) c.605del (p.Thr202SerfsTer19) | gnomAD v4 |
| 2 | g.29222407G>A | CA341488 | ALK | c.3452C>T (p.Thr1151Met) c.679C>T n.329C>T c.248C>T (p.Thr83Met) c.332C>T (p.Thr111Met) c.146C>T (p.Thr49Met) c.2321C>T (p.Thr774Met) c.605C>T (p.Thr202Met) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 2 | g.29222407G>C | CA1593928 | ALK | c.3452C>G (p.Thr1151Arg) c.679C>G n.329C>G c.248C>G (p.Thr83Arg) c.332C>G (p.Thr111Arg) c.146C>G (p.Thr49Arg) c.2321C>G (p.Thr774Arg) c.605C>G (p.Thr202Arg) | dbSNP ExAC gnomAD v2 |
| 2 | g.29222407G= | CA1241090538 | ALK | c.3452C= (p.Thr1151=) c.679C= n.329C= c.248C= (p.Thr83=) c.332C= (p.Thr111=) c.146C= (p.Thr49=) c.2321C= (p.Thr774=) c.605C= (p.Thr202=) | |
| 2 | g.29222407G>T | CA346463347 | ALK | c.3452C>A (p.Thr1151Lys) c.679C>A n.329C>A c.248C>A (p.Thr83Lys) c.332C>A (p.Thr111Lys) c.146C>A (p.Thr49Lys) c.2321C>A (p.Thr774Lys) c.605C>A (p.Thr202Lys) | dbSNP |
| 2 | g.29222408T>A | CA346463352 | ALK | c.3451A>T (p.Thr1151Ser) c.678A>T n.328A>T c.247A>T (p.Thr83Ser) c.331A>T (p.Thr111Ser) c.145A>T (p.Thr49Ser) c.2320A>T (p.Thr774Ser) c.604A>T (p.Thr202Ser) | dbSNP |
| 2 | g.29222408T>C | CA346463356 | ALK | c.3451A>G (p.Thr1151Ala) c.678A>G n.328A>G c.247A>G (p.Thr83Ala) c.331A>G (p.Thr111Ala) c.145A>G (p.Thr49Ala) c.2320A>G (p.Thr774Ala) c.604A>G (p.Thr202Ala) | dbSNP |
| 2 | g.29222408T>G | CA346463359 | ALK | c.3451A>C (p.Thr1151Pro) c.678A>C n.328A>C c.247A>C (p.Thr83Pro) c.331A>C (p.Thr111Pro) c.145A>C (p.Thr49Pro) c.2320A>C (p.Thr774Pro) c.604A>C (p.Thr202Pro) | ClinVar dbSNP gnomAD v4 |
| 2 | g.29222408T= | CA1241090539 | ALK | c.3451A= (p.Thr1151=) c.678A= n.328A= c.247A= (p.Thr83=) c.331A= (p.Thr111=) c.145A= (p.Thr49=) c.2320A= (p.Thr774=) c.604A= (p.Thr202=) | |
| 2 | g.29222409C>A | CA346463361 | ALK | c.3451-1G>T (n.3451-1G>T) c.678-1G>T n.328-1G>T c.247-1G>T (n.247-1G>T) c.331-1G>T (n.331-1G>T) c.145-1G>T (n.145-1G>T) c.2320-1G>T (n.2320-1G>T) c.604-1G>T (n.604-1G>T) | |
| 2 | g.29222409C>G | CA346463371 | ALK | c.3451-1G>C (n.3451-1G>C) c.678-1G>C n.328-1G>C c.247-1G>C (n.247-1G>C) c.331-1G>C (n.331-1G>C) c.145-1G>C (n.145-1G>C) c.2320-1G>C (n.2320-1G>C) c.604-1G>C (n.604-1G>C) | dbSNP |
| 2 | g.29222409C>T | CA346463373 | ALK | c.3451-1G>A (n.3451-1G>A) c.678-1G>A n.328-1G>A c.247-1G>A (n.247-1G>A) c.331-1G>A (n.331-1G>A) c.145-1G>A (n.145-1G>A) c.2320-1G>A (n.2320-1G>A) c.604-1G>A (n.604-1G>A) | dbSNP |
| 2 | g.29222410T>A | CA346463376 | ALK | c.3451-2A>T (n.3451-2A>T) c.678-2A>T n.328-2A>T c.247-2A>T (n.247-2A>T) c.331-2A>T (n.331-2A>T) c.145-2A>T (n.145-2A>T) c.2320-2A>T (n.2320-2A>T) c.604-2A>T (n.604-2A>T) | |
| 2 | g.29222410T>C | CA346463377 | ALK | c.3451-2A>G (n.3451-2A>G) c.678-2A>G n.328-2A>G c.247-2A>G (n.247-2A>G) c.331-2A>G (n.331-2A>G) c.145-2A>G (n.145-2A>G) c.2320-2A>G (n.2320-2A>G) c.604-2A>G (n.604-2A>G) | |
| 2 | g.29222410T>G | CA346463380 | ALK | c.3451-2A>C (n.3451-2A>C) c.678-2A>C n.328-2A>C c.247-2A>C (n.247-2A>C) c.331-2A>C (n.331-2A>C) c.145-2A>C (n.145-2A>C) c.2320-2A>C (n.2320-2A>C) c.604-2A>C (n.604-2A>C) | |
| 2 | g.29222411G>A | CA2580066298 | ALK | c.3451-3C>T (n.3451-3C>T) c.678-3C>T n.328-3C>T c.247-3C>T (n.247-3C>T) c.331-3C>T (n.331-3C>T) c.145-3C>T (n.145-3C>T) c.2320-3C>T (n.2320-3C>T) c.604-3C>T (n.604-3C>T) | ClinVar dbSNP |
| 2 | g.29222411G>C | CA2580066299 | ALK | c.3451-3C>G (n.3451-3C>G) c.678-3C>G n.328-3C>G c.247-3C>G (n.247-3C>G) c.331-3C>G (n.331-3C>G) c.145-3C>G (n.145-3C>G) c.2320-3C>G (n.2320-3C>G) c.604-3C>G (n.604-3C>G) | ClinVar dbSNP |
| 2 | g.29222411G>T | CA2698973241 | ALK | c.3451-3C>A (n.3451-3C>A) c.678-3C>A n.328-3C>A c.247-3C>A (n.247-3C>A) c.331-3C>A (n.331-3C>A) c.145-3C>A (n.145-3C>A) c.2320-3C>A (n.2320-3C>A) c.604-3C>A (n.604-3C>A) | dbSNP |
| 2 | g.29222412G>A | CA2698973247 | ALK | c.3451-4C>T (n.3451-4C>T) c.678-4C>T n.328-4C>T c.247-4C>T (n.247-4C>T) c.331-4C>T (n.331-4C>T) c.145-4C>T (n.145-4C>T) c.2320-4C>T (n.2320-4C>T) c.604-4C>T (n.604-4C>T) | dbSNP |
| 2 | g.29222412G>C | CA2698973246 | ALK | c.3451-4C>G (n.3451-4C>G) c.678-4C>G n.328-4C>G c.247-4C>G (n.247-4C>G) c.331-4C>G (n.331-4C>G) c.145-4C>G (n.145-4C>G) c.2320-4C>G (n.2320-4C>G) c.604-4C>G (n.604-4C>G) | dbSNP |
| 2 | g.29222412G>T | CA2698973245 | ALK | c.3451-4C>A (n.3451-4C>A) c.678-4C>A n.328-4C>A c.247-4C>A (n.247-4C>A) c.331-4C>A (n.331-4C>A) c.145-4C>A (n.145-4C>A) c.2320-4C>A (n.2320-4C>A) c.604-4C>A (n.604-4C>A) | dbSNP |
| 2 | g.29222413G>A | CA2580066300 | ALK | c.3451-5C>T (n.3451-5C>T) c.678-5C>T n.328-5C>T c.247-5C>T (n.247-5C>T) c.331-5C>T (n.331-5C>T) c.145-5C>T (n.145-5C>T) c.2320-5C>T (n.2320-5C>T) c.604-5C>T (n.604-5C>T) | ClinVar dbSNP |
| 2 | g.29222413G>C | CA2698973252 | ALK | c.3451-5C>G (n.3451-5C>G) c.678-5C>G n.328-5C>G c.247-5C>G (n.247-5C>G) c.331-5C>G (n.331-5C>G) c.145-5C>G (n.145-5C>G) c.2320-5C>G (n.2320-5C>G) c.604-5C>G (n.604-5C>G) | dbSNP |
| 2 | g.29222413G>T | CA2698973249 | ALK | c.3451-5C>A (n.3451-5C>A) c.678-5C>A n.328-5C>A c.247-5C>A (n.247-5C>A) c.331-5C>A (n.331-5C>A) c.145-5C>A (n.145-5C>A) c.2320-5C>A (n.2320-5C>A) c.604-5C>A (n.604-5C>A) | dbSNP |
| 2 | g.29222414C>A | CA2698973258 | ALK | c.3451-6G>T (n.3451-6G>T) c.678-6G>T n.328-6G>T c.247-6G>T (n.247-6G>T) c.331-6G>T (n.331-6G>T) c.145-6G>T (n.145-6G>T) c.2320-6G>T (n.2320-6G>T) c.604-6G>T (n.604-6G>T) | dbSNP |
| 2 | g.29222414C>G | CA2698973344 | ALK | c.3451-6G>C (n.3451-6G>C) c.678-6G>C n.328-6G>C c.247-6G>C (n.247-6G>C) c.331-6G>C (n.331-6G>C) c.145-6G>C (n.145-6G>C) c.2320-6G>C (n.2320-6G>C) c.604-6G>C (n.604-6G>C) | dbSNP |
| 2 | g.29222414C>T | CA2580066301 | ALK | c.3451-6G>A (n.3451-6G>A) c.678-6G>A n.328-6G>A c.247-6G>A (n.247-6G>A) c.331-6G>A (n.331-6G>A) c.145-6G>A (n.145-6G>A) c.2320-6G>A (n.2320-6G>A) c.604-6G>A (n.604-6G>A) | ClinVar dbSNP |
| 2 | g.29222415A>T | CA2698973388 | ALK | c.3451-7T>A (n.3451-7T>A) c.678-7T>A n.328-7T>A c.247-7T>A (n.247-7T>A) c.331-7T>A (n.331-7T>A) c.145-7T>A (n.145-7T>A) c.2320-7T>A (n.2320-7T>A) c.604-7T>A (n.604-7T>A) | dbSNP |
| 2 | g.29222416G>A | CA531766914 | ALK | c.3451-8C>T (n.3451-8C>T) c.678-8C>T n.328-8C>T c.247-8C>T (n.247-8C>T) c.331-8C>T (n.331-8C>T) c.145-8C>T (n.145-8C>T) c.2320-8C>T (n.2320-8C>T) c.604-8C>T (n.604-8C>T) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 2 | g.29222416G>C | CA2658458348 | ALK | c.3451-8C>G (n.3451-8C>G) c.678-8C>G n.328-8C>G c.247-8C>G (n.247-8C>G) c.331-8C>G (n.331-8C>G) c.145-8C>G (n.145-8C>G) c.2320-8C>G (n.2320-8C>G) c.604-8C>G (n.604-8C>G) | gnomAD v4 |
| 2 | g.29222416G= | CA1241090540 | ALK | c.3451-8C= (n.3451-8C=) c.678-8C= n.328-8C= c.247-8C= (n.247-8C=) c.331-8C= (n.331-8C=) c.145-8C= (n.145-8C=) c.2320-8C= (n.2320-8C=) c.604-8C= (n.604-8C=) | |
| 2 | g.29222416G>T | CA2698795493 | ALK | c.3451-8C>A (n.3451-8C>A) c.678-8C>A n.328-8C>A c.247-8C>A (n.247-8C>A) c.331-8C>A (n.331-8C>A) c.145-8C>A (n.145-8C>A) c.2320-8C>A (n.2320-8C>A) c.604-8C>A (n.604-8C>A) | dbSNP |
| 2 | g.29222418G>T | CA2698973402 | ALK | c.3451-10C>A (n.3451-10C>A) c.678-10C>A n.328-10C>A c.247-10C>A (n.247-10C>A) c.331-10C>A (n.331-10C>A) c.145-10C>A (n.145-10C>A) c.2320-10C>A (n.2320-10C>A) c.604-10C>A (n.604-10C>A) | dbSNP |
| 2 | g.29222419A= | CA1241090541 | ALK | c.3451-11T= (n.3451-11T=) c.678-11T= n.328-11T= c.247-11T= (n.247-11T=) c.331-11T= (n.331-11T=) c.145-11T= (n.145-11T=) c.2320-11T= (n.2320-11T=) c.604-11T= (n.604-11T=) | |
| 2 | g.29222419A>G | CA1593929 | ALK | c.3451-11T>C (n.3451-11T>C) c.678-11T>C n.328-11T>C c.247-11T>C (n.247-11T>C) c.331-11T>C (n.331-11T>C) c.145-11T>C (n.145-11T>C) c.2320-11T>C (n.2320-11T>C) c.604-11T>C (n.604-11T>C) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 2 | g.29222420A= | CA1241090542 | ALK | c.3451-12T= (n.3451-12T=) c.678-12T= n.328-12T= c.247-12T= (n.247-12T=) c.331-12T= (n.331-12T=) c.145-12T= (n.145-12T=) c.2320-12T= (n.2320-12T=) c.604-12T= (n.604-12T=) | |
| 2 | g.29222420A>G | CA2658458349 | ALK | c.3451-12T>C (n.3451-12T>C) c.678-12T>C n.328-12T>C c.247-12T>C (n.247-12T>C) c.331-12T>C (n.331-12T>C) c.145-12T>C (n.145-12T>C) c.2320-12T>C (n.2320-12T>C) c.604-12T>C (n.604-12T>C) | gnomAD v4 |
| 2 | g.29222420A>T | CA2576925295 | ALK | c.3451-12T>A (n.3451-12T>A) c.678-12T>A n.328-12T>A c.247-12T>A (n.247-12T>A) c.331-12T>A (n.331-12T>A) c.145-12T>A (n.145-12T>A) c.2320-12T>A (n.2320-12T>A) c.604-12T>A (n.604-12T>A) | dbSNP |
| 2 | g.29222421G>A | CA767513310 | ALK | c.3451-13C>T (n.3451-13C>T) c.678-13C>T n.328-13C>T c.247-13C>T (n.247-13C>T) c.331-13C>T (n.331-13C>T) c.145-13C>T (n.145-13C>T) c.2320-13C>T (n.2320-13C>T) c.604-13C>T (n.604-13C>T) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 2 | g.29222421G>C | CA2698796405 | ALK | c.3451-13C>G (n.3451-13C>G) c.678-13C>G n.328-13C>G c.247-13C>G (n.247-13C>G) c.331-13C>G (n.331-13C>G) c.145-13C>G (n.145-13C>G) c.2320-13C>G (n.2320-13C>G) c.604-13C>G (n.604-13C>G) | dbSNP |
| 2 | g.29222421G= | CA1241090543 | ALK | c.3451-13C= (n.3451-13C=) c.678-13C= n.328-13C= c.247-13C= (n.247-13C=) c.331-13C= (n.331-13C=) c.145-13C= (n.145-13C=) c.2320-13C= (n.2320-13C=) c.604-13C= (n.604-13C=) | |
| 2 | g.29222421G>T | CA2698796404 | ALK | c.3451-13C>A (n.3451-13C>A) c.678-13C>A n.328-13C>A c.247-13C>A (n.247-13C>A) c.331-13C>A (n.331-13C>A) c.145-13C>A (n.145-13C>A) c.2320-13C>A (n.2320-13C>A) c.604-13C>A (n.604-13C>A) | dbSNP |
| 2 | g.29222424dup | CA1593930 | ALK | c.3451-13dup (n.3451-13dup) c.678-13dup n.328-13dup c.247-13dup (n.247-13dup) c.331-13dup (n.331-13dup) c.145-13dup (n.145-13dup) c.2320-13dup (n.2320-13dup) c.604-13dup (n.604-13dup) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 2 | g.29222422G>A | CA2698973576 | ALK | c.3451-14C>T (n.3451-14C>T) c.678-14C>T n.328-14C>T c.247-14C>T (n.247-14C>T) c.331-14C>T (n.331-14C>T) c.145-14C>T (n.145-14C>T) c.2320-14C>T (n.2320-14C>T) c.604-14C>T (n.604-14C>T) | dbSNP |
| 2 | g.29222422G>C | CA2573134534 | ALK | c.3451-14C>G (n.3451-14C>G) c.678-14C>G n.328-14C>G c.247-14C>G (n.247-14C>G) c.331-14C>G (n.331-14C>G) c.145-14C>G (n.145-14C>G) c.2320-14C>G (n.2320-14C>G) c.604-14C>G (n.604-14C>G) | ClinVar dbSNP |
| 2 | g.29222422G>T | CA2698973601 | ALK | c.3451-14C>A (n.3451-14C>A) c.678-14C>A n.328-14C>A c.247-14C>A (n.247-14C>A) c.331-14C>A (n.331-14C>A) c.145-14C>A (n.145-14C>A) c.2320-14C>A (n.2320-14C>A) c.604-14C>A (n.604-14C>A) | dbSNP |
| 2 | g.29222423G>A | CA2698973693 | ALK | c.3451-15C>T (n.3451-15C>T) c.678-15C>T n.328-15C>T c.247-15C>T (n.247-15C>T) c.331-15C>T (n.331-15C>T) c.145-15C>T (n.145-15C>T) c.2320-15C>T (n.2320-15C>T) c.604-15C>T (n.604-15C>T) | dbSNP |
| 2 | g.29222423G>C | CA2698973663 | ALK | c.3451-15C>G (n.3451-15C>G) c.678-15C>G n.328-15C>G c.247-15C>G (n.247-15C>G) c.331-15C>G (n.331-15C>G) c.145-15C>G (n.145-15C>G) c.2320-15C>G (n.2320-15C>G) c.604-15C>G (n.604-15C>G) | dbSNP |
| 2 | g.29222423G>T | CA2698973657 | ALK | c.3451-15C>A (n.3451-15C>A) c.678-15C>A n.328-15C>A c.247-15C>A (n.247-15C>A) c.331-15C>A (n.331-15C>A) c.145-15C>A (n.145-15C>A) c.2320-15C>A (n.2320-15C>A) c.604-15C>A (n.604-15C>A) | dbSNP |
| 2 | g.29222424G>A | CA2658458354 | ALK | c.3451-16C>T (n.3451-16C>T) c.678-16C>T n.328-16C>T c.247-16C>T (n.247-16C>T) c.331-16C>T (n.331-16C>T) c.145-16C>T (n.145-16C>T) c.2320-16C>T (n.2320-16C>T) c.604-16C>T (n.604-16C>T) | gnomAD v4 |
| 2 | g.29222424G>C | CA1593931 | ALK | c.3451-16C>G (n.3451-16C>G) c.678-16C>G n.328-16C>G c.247-16C>G (n.247-16C>G) c.331-16C>G (n.331-16C>G) c.145-16C>G (n.145-16C>G) c.2320-16C>G (n.2320-16C>G) c.604-16C>G (n.604-16C>G) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 2 | g.29222424G= | CA1241090544 | ALK | c.3451-16C= (n.3451-16C=) c.678-16C= n.328-16C= c.247-16C= (n.247-16C=) c.331-16C= (n.331-16C=) c.145-16C= (n.145-16C=) c.2320-16C= (n.2320-16C=) c.604-16C= (n.604-16C=) | |
| 2 | g.29222425A= | CA1241090545 | ALK | c.3451-17T= (n.3451-17T=) c.678-17T= n.328-17T= c.247-17T= (n.247-17T=) c.331-17T= (n.331-17T=) c.145-17T= (n.145-17T=) c.2320-17T= (n.2320-17T=) c.604-17T= (n.604-17T=) | |
| 2 | g.29222425A>C | CA1593932 | ALK | c.3451-17T>G (n.3451-17T>G) c.678-17T>G n.328-17T>G c.247-17T>G (n.247-17T>G) c.331-17T>G (n.331-17T>G) c.145-17T>G (n.145-17T>G) c.2320-17T>G (n.2320-17T>G) c.604-17T>G (n.604-17T>G) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 2 | g.29222425A>T | CA2576925296 | ALK | c.3451-17T>A (n.3451-17T>A) c.678-17T>A n.328-17T>A c.247-17T>A (n.247-17T>A) c.331-17T>A (n.331-17T>A) c.145-17T>A (n.145-17T>A) c.2320-17T>A (n.2320-17T>A) c.604-17T>A (n.604-17T>A) | dbSNP gnomAD v4 |
| 2 | g.29222426G>A | CA1241090547 | ALK | c.3451-18C>T (n.3451-18C>T) c.678-18C>T n.328-18C>T c.247-18C>T (n.247-18C>T) c.331-18C>T (n.331-18C>T) c.145-18C>T (n.145-18C>T) c.2320-18C>T (n.2320-18C>T) c.604-18C>T (n.604-18C>T) | dbSNP |
| 2 | g.29222426G>C | CA2698823713 | ALK | c.3451-18C>G (n.3451-18C>G) c.678-18C>G n.328-18C>G c.247-18C>G (n.247-18C>G) c.331-18C>G (n.331-18C>G) c.145-18C>G (n.145-18C>G) c.2320-18C>G (n.2320-18C>G) c.604-18C>G (n.604-18C>G) | dbSNP |
| 2 | g.29222426G= | CA1241090546 | ALK | c.3451-18C= (n.3451-18C=) c.678-18C= n.328-18C= c.247-18C= (n.247-18C=) c.331-18C= (n.331-18C=) c.145-18C= (n.145-18C=) c.2320-18C= (n.2320-18C=) c.604-18C= (n.604-18C=) | |
| 2 | g.29222426G>T | CA2698823712 | ALK | c.3451-18C>A (n.3451-18C>A) c.678-18C>A n.328-18C>A c.247-18C>A (n.247-18C>A) c.331-18C>A (n.331-18C>A) c.145-18C>A (n.145-18C>A) c.2320-18C>A (n.2320-18C>A) c.604-18C>A (n.604-18C>A) | dbSNP |
| 2 | g.29222428del | CA2658458363 | ALK | c.3451-18del (n.3451-18del) c.678-18del n.328-18del c.247-18del (n.247-18del) c.331-18del (n.331-18del) c.145-18del (n.145-18del) c.2320-18del (n.2320-18del) c.604-18del (n.604-18del) | ClinVar gnomAD v4 |
| 2 | g.29222427G>A | CA2580066304 | ALK | c.3451-19C>T (n.3451-19C>T) c.678-19C>T n.328-19C>T c.247-19C>T (n.247-19C>T) c.331-19C>T (n.331-19C>T) c.145-19C>T (n.145-19C>T) c.2320-19C>T (n.2320-19C>T) c.604-19C>T (n.604-19C>T) | ClinVar dbSNP |
| 2 | g.29222427G>C | CA2698973757 | ALK | c.3451-19C>G (n.3451-19C>G) c.678-19C>G n.328-19C>G c.247-19C>G (n.247-19C>G) c.331-19C>G (n.331-19C>G) c.145-19C>G (n.145-19C>G) c.2320-19C>G (n.2320-19C>G) c.604-19C>G (n.604-19C>G) | dbSNP |
| 2 | g.29222428G>A | CA531766915 | ALK | c.3451-20C>T (n.3451-20C>T) c.678-20C>T n.328-20C>T c.247-20C>T (n.247-20C>T) c.331-20C>T (n.331-20C>T) c.145-20C>T (n.145-20C>T) c.2320-20C>T (n.2320-20C>T) c.604-20C>T (n.604-20C>T) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 2 | g.29222428G= | CA1241090548 | ALK | c.3451-20C= (n.3451-20C=) c.678-20C= n.328-20C= c.247-20C= (n.247-20C=) c.331-20C= (n.331-20C=) c.145-20C= (n.145-20C=) c.2320-20C= (n.2320-20C=) c.604-20C= (n.604-20C=) | |
| 2 | g.29222429T>A | CA2698809517 | ALK | c.3451-21A>T (n.3451-21A>T) c.678-21A>T n.328-21A>T c.247-21A>T (n.247-21A>T) c.331-21A>T (n.331-21A>T) c.145-21A>T (n.145-21A>T) c.2320-21A>T (n.2320-21A>T) c.604-21A>T (n.604-21A>T) | dbSNP |
| 2 | g.29222429T>G | CA1241090550 | ALK | c.3451-21A>C (n.3451-21A>C) c.678-21A>C n.328-21A>C c.247-21A>C (n.247-21A>C) c.331-21A>C (n.331-21A>C) c.145-21A>C (n.145-21A>C) c.2320-21A>C (n.2320-21A>C) c.604-21A>C (n.604-21A>C) | dbSNP gnomAD v4 |
| 2 | g.29222429T= | CA1241090549 | ALK | c.3451-21A= (n.3451-21A=) c.678-21A= n.328-21A= c.247-21A= (n.247-21A=) c.331-21A= (n.331-21A=) c.145-21A= (n.145-21A=) c.2320-21A= (n.2320-21A=) c.604-21A= (n.604-21A=) | |
| 2 | g.29222430G>A | CA1593933 | ALK | c.3451-22C>T (n.3451-22C>T) c.678-22C>T n.328-22C>T c.247-22C>T (n.247-22C>T) c.331-22C>T (n.331-22C>T) c.145-22C>T (n.145-22C>T) c.2320-22C>T (n.2320-22C>T) c.604-22C>T (n.604-22C>T) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 2 | g.29222430G= | CA1241090551 | ALK | c.3451-22C= (n.3451-22C=) c.678-22C= n.328-22C= c.247-22C= (n.247-22C=) c.331-22C= (n.331-22C=) c.145-22C= (n.145-22C=) c.2320-22C= (n.2320-22C=) c.604-22C= (n.604-22C=) | |
| 2 | g.29222431_29222436del | CA2658458369 | ALK | c.3451-27_3451-22del (n.3451-27_3451-22del) c.678-27_678-22del n.328-27_328-22del c.247-27_247-22del (n.247-27_247-22del) c.331-27_331-22del (n.331-27_331-22del) c.145-27_145-22del (n.145-27_145-22del) c.2320-27_2320-22del (n.2320-27_2320-22del) c.604-27_604-22del (n.604-27_604-22del) | gnomAD v4 |
| 2 | g.29222431G>T | CA2576925297 | ALK | c.3451-23C>A (n.3451-23C>A) c.678-23C>A n.328-23C>A c.247-23C>A (n.247-23C>A) c.331-23C>A (n.331-23C>A) c.145-23C>A (n.145-23C>A) c.2320-23C>A (n.2320-23C>A) c.604-23C>A (n.604-23C>A) | |
| 2 | g.29222431_29222434delinsGGGA | CA1241090552 | ALK | c.3451-26_3451-23delinsTCCC (n.3451-26_3451-23delinsTCCC) c.678-26_678-23delinsTCCC n.328-26_328-23delinsTCCC c.247-26_247-23delinsTCCC (n.247-26_247-23delinsTCCC) c.331-26_331-23delinsTCCC (n.331-26_331-23delinsTCCC) c.145-26_145-23delinsTCCC (n.145-26_145-23delinsTCCC) c.2320-26_2320-23delinsTCCC (n.2320-26_2320-23delinsTCCC) c.604-26_604-23delinsTCCC (n.604-26_604-23delinsTCCC) | |
| 2 | g.29222432G>A | CA2576925298 | ALK | c.3451-24C>T (n.3451-24C>T) c.678-24C>T n.328-24C>T c.247-24C>T (n.247-24C>T) c.331-24C>T (n.331-24C>T) c.145-24C>T (n.145-24C>T) c.2320-24C>T (n.2320-24C>T) c.604-24C>T (n.604-24C>T) | dbSNP gnomAD v4 |
| 2 | g.29222432G>C | CA2698809518 | ALK | c.3451-24C>G (n.3451-24C>G) c.678-24C>G n.328-24C>G c.247-24C>G (n.247-24C>G) c.331-24C>G (n.331-24C>G) c.145-24C>G (n.145-24C>G) c.2320-24C>G (n.2320-24C>G) c.604-24C>G (n.604-24C>G) | dbSNP |
| 2 | g.29222432G= | CA1241090554 | ALK | c.3451-24C= (n.3451-24C=) c.678-24C= n.328-24C= c.247-24C= (n.247-24C=) c.331-24C= (n.331-24C=) c.145-24C= (n.145-24C=) c.2320-24C= (n.2320-24C=) c.604-24C= (n.604-24C=) | |
| 2 | g.29222432G>T | CA1241090553 | ALK | c.3451-24C>A (n.3451-24C>A) c.678-24C>A n.328-24C>A c.247-24C>A (n.247-24C>A) c.331-24C>A (n.331-24C>A) c.145-24C>A (n.145-24C>A) c.2320-24C>A (n.2320-24C>A) c.604-24C>A (n.604-24C>A) | dbSNP |
| 2 | g.29222443_29222445dup | CA44631260 | ALK | c.3451-26_3451-24dup (n.3451-26_3451-24dup) c.678-26_678-24dup n.328-26_328-24dup c.247-26_247-24dup (n.247-26_247-24dup) c.331-26_331-24dup (n.331-26_331-24dup) c.145-26_145-24dup (n.145-26_145-24dup) c.2320-26_2320-24dup (n.2320-26_2320-24dup) c.604-26_604-24dup (n.604-26_604-24dup) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 2 | g.29222443_29222445del | CA1593934 | ALK | c.3451-26_3451-24del (n.3451-26_3451-24del) c.678-26_678-24del n.328-26_328-24del c.247-26_247-24del (n.247-26_247-24del) c.331-26_331-24del (n.331-26_331-24del) c.145-26_145-24del (n.145-26_145-24del) c.2320-26_2320-24del (n.2320-26_2320-24del) c.604-26_604-24del (n.604-26_604-24del) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |