| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 2 | g.29220735A>C | CA346472999 | ALK | c.3616T>G (p.Ser1206Ala) c.843T>G n.493T>G c.412T>G (p.Ser138Ala) c.496T>G (p.Ser166Ala) c.2485T>G (p.Ser829Ala) c.769T>G (p.Ser257Ala) | ClinVar |
| 2 | g.29220735A>G | CA346473000 | ALK | c.3616T>C (p.Ser1206Pro) c.843T>C n.493T>C c.412T>C (p.Ser138Pro) c.496T>C (p.Ser166Pro) c.2485T>C (p.Ser829Pro) c.769T>C (p.Ser257Pro) | gnomAD v4 |
| 2 | g.29220735A>T | CA346473001 | ALK | c.3616T>A (p.Ser1206Thr) c.843T>A n.493T>A c.412T>A (p.Ser138Thr) c.496T>A (p.Ser166Thr) c.2485T>A (p.Ser829Thr) c.769T>A (p.Ser257Thr) | |
| 2 | g.29220736C>A | CA346473002 | ALK | c.3615G>T (p.Lys1205Asn) c.842G>T n.492G>T c.411G>T (p.Lys137Asn) c.495G>T (p.Lys165Asn) c.2484G>T (p.Lys828Asn) c.768G>T (p.Lys256Asn) | |
| 2 | g.29220736C>G | CA346473003 | ALK | c.3615G>C (p.Lys1205Asn) c.842G>C n.492G>C c.411G>C (p.Lys137Asn) c.495G>C (p.Lys165Asn) c.2484G>C (p.Lys828Asn) c.768G>C (p.Lys256Asn) | dbSNP |
| 2 | g.29220736C>T | CA425435441 | ALK | c.3615G>A (p.Lys1205=) c.842G>A n.492G>A c.411G>A (p.Lys137=) c.495G>A (p.Lys165=) c.2484G>A (p.Lys828=) c.768G>A (p.Lys256=) | dbSNP |
| 2 | g.29220737T>A | CA346473004 | ALK | c.3614A>T (p.Lys1205Met) c.841A>T n.491A>T c.410A>T (p.Lys137Met) c.494A>T (p.Lys165Met) c.2483A>T (p.Lys828Met) c.767A>T (p.Lys256Met) | dbSNP |
| 2 | g.29220737T>C | CA346473006 | ALK | c.3614A>G (p.Lys1205Arg) c.841A>G n.491A>G c.410A>G (p.Lys137Arg) c.494A>G (p.Lys165Arg) c.2483A>G (p.Lys828Arg) c.767A>G (p.Lys256Arg) | ClinVar dbSNP |
| 2 | g.29220737T>G | CA346473005 | ALK | c.3614A>C (p.Lys1205Thr) c.841A>C n.491A>C c.410A>C (p.Lys137Thr) c.494A>C (p.Lys165Thr) c.2483A>C (p.Lys828Thr) c.767A>C (p.Lys256Thr) | |
| 2 | g.29220738T>A | CA346473007 | ALK | c.3613A>T (p.Lys1205Ter) c.840A>T n.490A>T c.409A>T (p.Lys137Ter) c.493A>T (p.Lys165Ter) c.2482A>T (p.Lys828Ter) c.766A>T (p.Lys256Ter) | |
| 2 | g.29220738T>C | CA346473008 | ALK | c.3613A>G (p.Lys1205Glu) c.840A>G n.490A>G c.409A>G (p.Lys137Glu) c.493A>G (p.Lys165Glu) c.2482A>G (p.Lys828Glu) c.766A>G (p.Lys256Glu) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 2 | g.29220738T>G | CA346473009 | ALK | c.3613A>C (p.Lys1205Gln) c.840A>C n.490A>C c.409A>C (p.Lys137Gln) c.493A>C (p.Lys165Gln) c.2482A>C (p.Lys828Gln) c.766A>C (p.Lys256Gln) | |
| 2 | g.29220738T= | CA1241089758 | ALK | c.3613A= (p.Lys1205=) c.840A= n.490A= c.409A= (p.Lys137=) c.493A= (p.Lys165=) c.2482A= (p.Lys828=) c.766A= (p.Lys256=) | |
| 2 | g.29220739G>A | CA425619389 | ALK | c.3612C>T (p.Leu1204=) c.839C>T n.489C>T c.408C>T (p.Leu136=) c.492C>T (p.Leu164=) c.2481C>T (p.Leu827=) c.765C>T (p.Leu255=) | dbSNP |
| 2 | g.29220739G>C | CA425619387 | ALK | c.3612C>G (p.Leu1204=) c.839C>G n.489C>G c.408C>G (p.Leu136=) c.492C>G (p.Leu164=) c.2481C>G (p.Leu827=) c.765C>G (p.Leu255=) | ClinVar dbSNP COSMIC |
| 2 | g.29220739G>T | CA425619388 | ALK | c.3612C>A (p.Leu1204=) c.839C>A n.489C>A c.408C>A (p.Leu136=) c.492C>A (p.Leu164=) c.2481C>A (p.Leu827=) c.765C>A (p.Leu255=) | dbSNP |
| 2 | g.29220740A= | CA1241089759 | ALK | c.3611T= (p.Leu1204=) c.838T= n.488T= c.407T= (p.Leu136=) c.491T= (p.Leu164=) c.2480T= (p.Leu827=) c.764T= (p.Leu255=) | |
| 2 | g.29220740A>C | CA346473010 | ALK | c.3611T>G (p.Leu1204Arg) c.838T>G n.488T>G c.407T>G (p.Leu136Arg) c.491T>G (p.Leu164Arg) c.2480T>G (p.Leu827Arg) c.764T>G (p.Leu255Arg) | |
| 2 | g.29220740A>G | CA346473011 | ALK | c.3611T>C (p.Leu1204Pro) c.838T>C n.488T>C c.407T>C (p.Leu136Pro) c.491T>C (p.Leu164Pro) c.2480T>C (p.Leu827Pro) c.764T>C (p.Leu255Pro) | dbSNP |
| 2 | g.29220740A>T | CA346473012 | ALK | c.3611T>A (p.Leu1204His) c.838T>A n.488T>A c.407T>A (p.Leu136His) c.491T>A (p.Leu164His) c.2480T>A (p.Leu827His) c.764T>A (p.Leu255His) | dbSNP |
| 2 | g.29220741G>A | CA346473013 | ALK | c.3610C>T (p.Leu1204Phe) c.837C>T n.487C>T c.406C>T (p.Leu136Phe) c.490C>T (p.Leu164Phe) c.2479C>T (p.Leu827Phe) c.763C>T (p.Leu255Phe) | ClinVar dbSNP |
| 2 | g.29220741G>C | CA346473014 | ALK | c.3610C>G (p.Leu1204Val) c.837C>G n.487C>G c.406C>G (p.Leu136Val) c.490C>G (p.Leu164Val) c.2479C>G (p.Leu827Val) c.763C>G (p.Leu255Val) | ClinVar dbSNP gnomAD v4 |
| 2 | g.29220741G= | CA1241089760 | ALK | c.3610C= (p.Leu1204=) c.837C= n.487C= c.406C= (p.Leu136=) c.490C= (p.Leu164=) c.2479C= (p.Leu827=) c.763C= (p.Leu255=) | |
| 2 | g.29220741G>T | CA346473015 | ALK | c.3610C>A (p.Leu1204Ile) c.837C>A n.487C>A c.406C>A (p.Leu136Ile) c.490C>A (p.Leu164Ile) c.2479C>A (p.Leu827Ile) c.763C>A (p.Leu255Ile) | dbSNP |
| 2 | g.29220742G>A | CA425619390 | ALK | c.3609C>T (p.Asp1203=) c.836C>T n.486C>T c.405C>T (p.Asp135=) c.489C>T (p.Asp163=) c.2478C>T (p.Asp826=) c.762C>T (p.Asp254=) | dbSNP |
| 2 | g.29220742G>C | CA346473016 | ALK | c.3609C>G (p.Asp1203Glu) c.836C>G n.486C>G c.405C>G (p.Asp135Glu) c.489C>G (p.Asp163Glu) c.2478C>G (p.Asp826Glu) c.762C>G (p.Asp254Glu) | dbSNP |
| 2 | g.29220742G>T | CA346473017 | ALK | c.3609C>A (p.Asp1203Glu) c.836C>A n.486C>A c.405C>A (p.Asp135Glu) c.489C>A (p.Asp163Glu) c.2478C>A (p.Asp826Glu) c.762C>A (p.Asp254Glu) | ClinVar dbSNP |
| 2 | g.29220743T>A | CA346473020 | ALK | c.3608A>T (p.Asp1203Val) c.835A>T n.485A>T c.404A>T (p.Asp135Val) c.488A>T (p.Asp163Val) c.2477A>T (p.Asp826Val) c.761A>T (p.Asp254Val) | dbSNP |
| 2 | g.29220743T>C | CA346473018 | ALK | c.3608A>G (p.Asp1203Gly) c.835A>G n.485A>G c.404A>G (p.Asp135Gly) c.488A>G (p.Asp163Gly) c.2477A>G (p.Asp826Gly) c.761A>G (p.Asp254Gly) | ClinVar dbSNP |
| 2 | g.29220743T>G | CA346473019 | ALK | c.3608A>C (p.Asp1203Ala) c.835A>C n.485A>C c.404A>C (p.Asp135Ala) c.488A>C (p.Asp163Ala) c.2477A>C (p.Asp826Ala) c.761A>C (p.Asp254Ala) | ClinVar dbSNP |
| 2 | g.29220744C>A | CA346473021 | ALK | c.3607G>T (p.Asp1203Tyr) c.834G>T n.484G>T c.403G>T (p.Asp135Tyr) c.487G>T (p.Asp163Tyr) c.2476G>T (p.Asp826Tyr) c.760G>T (p.Asp254Tyr) | |
| 2 | g.29220744C= | CA1241089761 | ALK | c.3607G= (p.Asp1203=) c.834G= n.484G= c.403G= (p.Asp135=) c.487G= (p.Asp163=) c.2476G= (p.Asp826=) c.760G= (p.Asp254=) | |
| 2 | g.29220744C>G | CA346473022 | ALK | c.3607G>C (p.Asp1203His) c.834G>C n.484G>C c.403G>C (p.Asp135His) c.487G>C (p.Asp163His) c.2476G>C (p.Asp826His) c.760G>C (p.Asp254His) | ClinVar dbSNP gnomAD v4 |
| 2 | g.29220744C>T | CA1593847 | ALK | c.3607G>A (p.Asp1203Asn) c.834G>A n.484G>A c.403G>A (p.Asp135Asn) c.487G>A (p.Asp163Asn) c.2476G>A (p.Asp826Asn) c.760G>A (p.Asp254Asn) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 2 | g.29220745T>A | CA425619391 | ALK | c.3606A>T (p.Gly1202=) c.833A>T n.483A>T c.402A>T (p.Gly134=) c.486A>T (p.Gly162=) c.2475A>T (p.Gly825=) c.759A>T (p.Gly253=) | |
| 2 | g.29220745T>C | CA1593848 | ALK | c.3606A>G (p.Gly1202=) c.833A>G n.483A>G c.402A>G (p.Gly134=) c.486A>G (p.Gly162=) c.2475A>G (p.Gly825=) c.759A>G (p.Gly253=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 2 | g.29220745T>G | CA425619392 | ALK | c.3606A>C (p.Gly1202=) c.833A>C n.483A>C c.402A>C (p.Gly134=) c.486A>C (p.Gly162=) c.2475A>C (p.Gly825=) c.759A>C (p.Gly253=) | |
| 2 | g.29220745T= | CA1241089762 | ALK | c.3606A= (p.Gly1202=) c.833A= n.483A= c.402A= (p.Gly134=) c.486A= (p.Gly162=) c.2475A= (p.Gly825=) c.759A= (p.Gly253=) | |
| 2 | g.29220745dup | CA531766851 | ALK | c.3606dup (p.Asp1203ArgfsTer?) c.833dup n.483dup c.402dup (p.Asp135ArgfsTer?) c.486dup (p.Asp163ArgfsTer?) c.2475dup (p.Asp826ArgfsTer?) c.759dup (p.Asp254ArgfsTer?) | dbSNP gnomAD v2 gnomAD v4 |
| 2 | g.29220746C>A | CA346473023 | ALK | c.3605G>T (p.Gly1202Val) c.832G>T n.482G>T c.401G>T (p.Gly134Val) c.485G>T (p.Gly162Val) c.2474G>T (p.Gly825Val) c.758G>T (p.Gly253Val) | dbSNP |
| 2 | g.29220746C= | CA1241089763 | ALK | c.3605G= (p.Gly1202=) c.832G= n.482G= c.401G= (p.Gly134=) c.485G= (p.Gly162=) c.2474G= (p.Gly825=) c.758G= (p.Gly253=) | |
| 2 | g.29220746C>G | CA346473024 | ALK | c.3605G>C (p.Gly1202Ala) c.832G>C n.482G>C c.401G>C (p.Gly134Ala) c.485G>C (p.Gly162Ala) c.2474G>C (p.Gly825Ala) c.758G>C (p.Gly253Ala) | gnomAD v4 |
| 2 | g.29220746C>T | CA346473025 | ALK | c.3605G>A (p.Gly1202Glu) c.832G>A n.482G>A c.401G>A (p.Gly134Glu) c.485G>A (p.Gly162Glu) c.2474G>A (p.Gly825Glu) c.758G>A (p.Gly253Glu) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 2 | g.29220751dup | CA531766852 | ALK | c.3605dup (p.Asp1203ArgfsTer?) c.832dup n.482dup c.401dup (p.Asp135ArgfsTer?) c.485dup (p.Asp163ArgfsTer?) c.2474dup (p.Asp826ArgfsTer?) c.758dup (p.Asp254ArgfsTer?) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 2 | g.29220751del | CA2586968911 | ALK | c.3605del (p.Gly1202GlufsTer?) c.832del n.482del c.401del (p.Gly134GlufsTer?) c.485del (p.Gly162GlufsTer?) c.2474del (p.Gly825GlufsTer?) c.758del (p.Gly253GlufsTer?) | gnomAD v4 |
| 2 | g.29220749_29220751del | CA2698809495 | ALK | c.3603_3605del (p.Gly1202del) c.830_832del n.480_482del c.399_401del (p.Gly134del) c.483_485del (p.Gly162del) c.2472_2474del (p.Gly825del) c.756_758del (p.Gly253del) | dbSNP |
| 2 | g.29220747C>A | CA346473026 | ALK | c.3604G>T (p.Gly1202Ter) c.831G>T n.481G>T c.400G>T (p.Gly134Ter) c.484G>T (p.Gly162Ter) c.2473G>T (p.Gly825Ter) c.757G>T (p.Gly253Ter) | dbSNP |
| 2 | g.29220747C= | CA1241089764 | ALK | c.3604G= (p.Gly1202=) c.831G= n.481G= c.400G= (p.Gly134=) c.484G= (p.Gly162=) c.2473G= (p.Gly825=) c.757G= (p.Gly253=) | |
| 2 | g.29220747C>G | CA346473027 | ALK | c.3604G>C (p.Gly1202Arg) c.831G>C n.481G>C c.400G>C (p.Gly134Arg) c.484G>C (p.Gly162Arg) c.2473G>C (p.Gly825Arg) c.757G>C (p.Gly253Arg) | ClinVar dbSNP |
| 2 | g.29220747C>T | CA16602592 | ALK | c.3604G>A (p.Gly1202Arg) c.831G>A n.481G>A c.400G>A (p.Gly134Arg) c.484G>A (p.Gly162Arg) c.2473G>A (p.Gly825Arg) c.757G>A (p.Gly253Arg) | ClinVar dbSNP gnomAD v4 COSMIC |
| 2 | g.29220748C>A | CA425619394 | ALK | c.3603G>T (p.Gly1201=) c.830G>T n.480G>T c.399G>T (p.Gly133=) c.483G>T (p.Gly161=) c.2472G>T (p.Gly824=) c.756G>T (p.Gly252=) | dbSNP gnomAD v4 |
| 2 | g.29220748C= | CA1241089765 | ALK | c.3603G= (p.Gly1201=) c.830G= n.480G= c.399G= (p.Gly133=) c.483G= (p.Gly161=) c.2472G= (p.Gly824=) c.756G= (p.Gly252=) | |
| 2 | g.29220748C>G | CA425619393 | ALK | c.3603G>C (p.Gly1201=) c.830G>C n.480G>C c.399G>C (p.Gly133=) c.483G>C (p.Gly161=) c.2472G>C (p.Gly824=) c.756G>C (p.Gly252=) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 2 | g.29220748C>T | CA1593849 | ALK | c.3603G>A (p.Gly1201=) c.830G>A n.480G>A c.399G>A (p.Gly133=) c.483G>A (p.Gly161=) c.2472G>A (p.Gly824=) c.756G>A (p.Gly252=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 2 | g.29220748_29220749delinsTT | CA645528799 | ALK | c.3602_3603delinsAA (p.Gly1201Glu) c.829_830delinsAA n.479_480delinsAA c.398_399delinsAA (p.Gly133Glu) c.482_483delinsAA (p.Gly161Glu) c.2471_2472delinsAA (p.Gly824Glu) c.755_756delinsAA (p.Gly252Glu) | COSMIC |
| 2 | g.29220749C>A | CA346473029 | ALK | c.3602G>T (p.Gly1201Val) c.829G>T n.479G>T c.398G>T (p.Gly133Val) c.482G>T (p.Gly161Val) c.2471G>T (p.Gly824Val) c.755G>T (p.Gly252Val) | dbSNP gnomAD v2 gnomAD v4 |
| 2 | g.29220749C= | CA1241089766 | ALK | c.3602G= (p.Gly1201=) c.829G= n.479G= c.398G= (p.Gly133=) c.482G= (p.Gly161=) c.2471G= (p.Gly824=) c.755G= (p.Gly252=) | |
| 2 | g.29220749C>G | CA346473030 | ALK | c.3602G>C (p.Gly1201Ala) c.829G>C n.479G>C c.398G>C (p.Gly133Ala) c.482G>C (p.Gly161Ala) c.2471G>C (p.Gly824Ala) c.755G>C (p.Gly252Ala) | ClinVar dbSNP |
| 2 | g.29220749C>T | CA346473028 | ALK | c.3602G>A (p.Gly1201Glu) c.829G>A n.479G>A c.398G>A (p.Gly133Glu) c.482G>A (p.Gly161Glu) c.2471G>A (p.Gly824Glu) c.755G>A (p.Gly252Glu) | ClinVar dbSNP COSMIC |
| 2 | g.29220750C>A | CA346473032 | ALK | c.3601G>T (p.Gly1201Trp) c.828G>T n.478G>T c.397G>T (p.Gly133Trp) c.481G>T (p.Gly161Trp) c.2470G>T (p.Gly824Trp) c.754G>T (p.Gly252Trp) | ClinVar dbSNP gnomAD v4 |
| 2 | g.29220750C= | CA1241089767 | ALK | c.3601G= (p.Gly1201=) c.828G= n.478G= c.397G= (p.Gly133=) c.481G= (p.Gly161=) c.2470G= (p.Gly824=) c.754G= (p.Gly252=) | |
| 2 | g.29220750C>G | CA1593850 | ALK | c.3601G>C (p.Gly1201Arg) c.828G>C n.478G>C c.397G>C (p.Gly133Arg) c.481G>C (p.Gly161Arg) c.2470G>C (p.Gly824Arg) c.754G>C (p.Gly252Arg) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 2 | g.29220750C>T | CA346473031 | ALK | c.3601G>A (p.Gly1201Arg) c.828G>A n.478G>A c.397G>A (p.Gly133Arg) c.481G>A (p.Gly161Arg) c.2470G>A (p.Gly824Arg) c.754G>A (p.Gly252Arg) | ClinVar |
| 2 | g.29220751C>A | CA1593853 | ALK | c.3600G>T (p.Ala1200=) c.827G>T n.477G>T c.396G>T (p.Ala132=) c.480G>T (p.Ala160=) c.2469G>T (p.Ala823=) c.753G>T (p.Ala251=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 2 | g.29220751C= | CA1241089768 | ALK | c.3600G= (p.Ala1200=) c.827G= n.477G= c.396G= (p.Ala132=) c.480G= (p.Ala160=) c.2469G= (p.Ala823=) c.753G= (p.Ala251=) | |
| 2 | g.29220751C>G | CA1593851 | ALK | c.3600G>C (p.Ala1200=) c.827G>C n.477G>C c.396G>C (p.Ala132=) c.480G>C (p.Ala160=) c.2469G>C (p.Ala823=) c.753G>C (p.Ala251=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 2 | g.29220751C>T | CA1593852 | ALK | c.3600G>A (p.Ala1200=) c.827G>A n.477G>A c.396G>A (p.Ala132=) c.480G>A (p.Ala160=) c.2469G>A (p.Ala823=) c.753G>A (p.Ala251=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 2 | g.29220752G>A | CA1593854 | ALK | c.3599C>T (p.Ala1200Val) c.826C>T n.476C>T c.395C>T (p.Ala132Val) c.479C>T (p.Ala160Val) c.2468C>T (p.Ala823Val) c.752C>T (p.Ala251Val) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 2 | g.29220752G>C | CA1593855 | ALK | c.3599C>G (p.Ala1200Gly) c.826C>G n.476C>G c.395C>G (p.Ala132Gly) c.479C>G (p.Ala160Gly) c.2468C>G (p.Ala823Gly) c.752C>G (p.Ala251Gly) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 2 | g.29220752G= | CA1241089769 | ALK | c.3599C= (p.Ala1200=) c.826C= n.476C= c.395C= (p.Ala132=) c.479C= (p.Ala160=) c.2468C= (p.Ala823=) c.752C= (p.Ala251=) | |
| 2 | g.29220752G>T | CA346473033 | ALK | c.3599C>A (p.Ala1200Glu) c.826C>A n.476C>A c.395C>A (p.Ala132Glu) c.479C>A (p.Ala160Glu) c.2468C>A (p.Ala823Glu) c.752C>A (p.Ala251Glu) | |
| 2 | g.29220753C>A | CA346473034 | ALK | c.3598G>T (p.Ala1200Ser) c.825G>T n.475G>T c.394G>T (p.Ala132Ser) c.478G>T (p.Ala160Ser) c.2467G>T (p.Ala823Ser) c.751G>T (p.Ala251Ser) | |
| 2 | g.29220753C>G | CA346473035 | ALK | c.3598G>C (p.Ala1200Pro) c.825G>C n.475G>C c.394G>C (p.Ala132Pro) c.478G>C (p.Ala160Pro) c.2467G>C (p.Ala823Pro) c.751G>C (p.Ala251Pro) | dbSNP |
| 2 | g.29220753C>T | CA346473036 | ALK | c.3598G>A (p.Ala1200Thr) c.825G>A n.475G>A c.394G>A (p.Ala132Thr) c.478G>A (p.Ala160Thr) c.2467G>A (p.Ala823Thr) c.751G>A (p.Ala251Thr) | ClinVar dbSNP |
| 2 | g.29220754C>A | CA346473037 | ALK | c.3597G>T (p.Met1199Ile) c.824G>T n.474G>T c.393G>T (p.Met131Ile) c.477G>T (p.Met159Ile) c.2466G>T (p.Met822Ile) c.750G>T (p.Met250Ile) | ClinVar dbSNP |
| 2 | g.29220754C= | CA1241089770 | ALK | c.3597G= (p.Met1199=) c.824G= n.474G= c.393G= (p.Met131=) c.477G= (p.Met159=) c.2466G= (p.Met822=) c.750G= (p.Met250=) | |
| 2 | g.29220754C>G | CA346473038 | ALK | c.3597G>C (p.Met1199Ile) c.824G>C n.474G>C c.393G>C (p.Met131Ile) c.477G>C (p.Met159Ile) c.2466G>C (p.Met822Ile) c.750G>C (p.Met250Ile) | dbSNP |
| 2 | g.29220754C>T | CA346473039 | ALK | c.3597G>A (p.Met1199Ile) c.824G>A n.474G>A c.393G>A (p.Met131Ile) c.477G>A (p.Met159Ile) c.2466G>A (p.Met822Ile) c.750G>A (p.Met250Ile) | ClinVar dbSNP COSMIC |
| 2 | g.29220755A>C | CA346473040 | ALK | c.3596T>G (p.Met1199Arg) c.823T>G n.473T>G c.392T>G (p.Met131Arg) c.476T>G (p.Met159Arg) c.2465T>G (p.Met822Arg) c.749T>G (p.Met250Arg) | dbSNP |
| 2 | g.29220755A>G | CA346473042 | ALK | c.3596T>C (p.Met1199Thr) c.823T>C n.473T>C c.392T>C (p.Met131Thr) c.476T>C (p.Met159Thr) c.2465T>C (p.Met822Thr) c.749T>C (p.Met250Thr) | ClinVar dbSNP gnomAD v4 |
| 2 | g.29220755A>T | CA346473041 | ALK | c.3596T>A (p.Met1199Lys) c.823T>A n.473T>A c.392T>A (p.Met131Lys) c.476T>A (p.Met159Lys) c.2465T>A (p.Met822Lys) c.749T>A (p.Met250Lys) | dbSNP |
| 2 | g.29220756T>A | CA346473043 | ALK | c.3595A>T (p.Met1199Leu) c.822A>T n.472A>T c.391A>T (p.Met131Leu) c.475A>T (p.Met159Leu) c.2464A>T (p.Met822Leu) c.748A>T (p.Met250Leu) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 2 | g.29220756T>C | CA346473044 | ALK | c.3595A>G (p.Met1199Val) c.822A>G n.472A>G c.391A>G (p.Met131Val) c.475A>G (p.Met159Val) c.2464A>G (p.Met822Val) c.748A>G (p.Met250Val) | gnomAD v4 |
| 2 | g.29220756T>G | CA346473045 | ALK | c.3595A>C (p.Met1199Leu) c.822A>C n.472A>C c.391A>C (p.Met131Leu) c.475A>C (p.Met159Leu) c.2464A>C (p.Met822Leu) c.748A>C (p.Met250Leu) | ClinVar dbSNP gnomAD v4 |
| 2 | g.29220756T= | CA1241089771 | ALK | c.3595A= (p.Met1199=) c.822A= n.472A= c.391A= (p.Met131=) c.475A= (p.Met159=) c.2464A= (p.Met822=) c.748A= (p.Met250=) | |
| 2 | g.29220757G>A | CA1593856 | ALK | c.3594C>T (p.Leu1198=) c.821C>T n.471C>T c.390C>T (p.Leu130=) c.474C>T (p.Leu158=) c.2463C>T (p.Leu821=) c.747C>T (p.Leu249=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 2 | g.29220757G>C | CA425619395 | ALK | c.3594C>G (p.Leu1198=) c.821C>G n.471C>G c.390C>G (p.Leu130=) c.474C>G (p.Leu158=) c.2463C>G (p.Leu821=) c.747C>G (p.Leu249=) | dbSNP |
| 2 | g.29220757G= | CA1241089772 | ALK | c.3594C= (p.Leu1198=) c.821C= n.471C= c.390C= (p.Leu130=) c.474C= (p.Leu158=) c.2463C= (p.Leu821=) c.747C= (p.Leu249=) | |
| 2 | g.29220757G>T | CA425619396 | ALK | c.3594C>A (p.Leu1198=) c.821C>A n.471C>A c.390C>A (p.Leu130=) c.474C>A (p.Leu158=) c.2463C>A (p.Leu821=) c.747C>A (p.Leu249=) | dbSNP |
| 2 | g.29220758A= | CA1241089773 | ALK | c.3593T= (p.Leu1198=) c.820T= n.470T= c.389T= (p.Leu130=) c.473T= (p.Leu158=) c.2462T= (p.Leu821=) c.746T= (p.Leu249=) | |
| 2 | g.29220758A>C | CA346473046 | ALK | c.3593T>G (p.Leu1198Arg) c.820T>G n.470T>G c.389T>G (p.Leu130Arg) c.473T>G (p.Leu158Arg) c.2462T>G (p.Leu821Arg) c.746T>G (p.Leu249Arg) | |
| 2 | g.29220758A>G | CA346473047 | ALK | c.3593T>C (p.Leu1198Pro) c.820T>C n.470T>C c.389T>C (p.Leu130Pro) c.473T>C (p.Leu158Pro) c.2462T>C (p.Leu821Pro) c.746T>C (p.Leu249Pro) | dbSNP gnomAD v4 |
| 2 | g.29220758A>T | CA1593857 | ALK | c.3593T>A (p.Leu1198His) c.820T>A n.470T>A c.389T>A (p.Leu130His) c.473T>A (p.Leu158His) c.2462T>A (p.Leu821His) c.746T>A (p.Leu249His) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 2 | g.29220759G>A | CA346473048 | ALK | c.3592C>T (p.Leu1198Phe) c.819C>T n.469C>T c.388C>T (p.Leu130Phe) c.472C>T (p.Leu158Phe) c.2461C>T (p.Leu821Phe) c.745C>T (p.Leu249Phe) | dbSNP gnomAD v3 gnomAD v4 COSMIC |
| 2 | g.29220759G>C | CA346473049 | ALK | c.3592C>G (p.Leu1198Val) c.819C>G n.469C>G c.388C>G (p.Leu130Val) c.472C>G (p.Leu158Val) c.2461C>G (p.Leu821Val) c.745C>G (p.Leu249Val) | dbSNP |
| 2 | g.29220759G= | CA1241089774 | ALK | c.3592C= (p.Leu1198=) c.819C= n.469C= c.388C= (p.Leu130=) c.472C= (p.Leu158=) c.2461C= (p.Leu821=) c.745C= (p.Leu249=) | |
| 2 | g.29220759G>T | CA1593858 | ALK | c.3592C>A (p.Leu1198Ile) c.819C>A n.469C>A c.388C>A (p.Leu130Ile) c.472C>A (p.Leu158Ile) c.2461C>A (p.Leu821Ile) c.745C>A (p.Leu249Ile) | ClinVar dbSNP ExAC gnomAD v2 |
| 2 | g.29220760C>A | CA346473051 | ALK | c.3591G>T (p.Glu1197Asp) c.818G>T n.468G>T c.387G>T (p.Glu129Asp) c.471G>T (p.Glu157Asp) c.2460G>T (p.Glu820Asp) c.744G>T (p.Glu248Asp) | dbSNP |
| 2 | g.29220760C= | CA1241089775 | ALK | c.3591G= (p.Glu1197=) c.818G= n.468G= c.387G= (p.Glu129=) c.471G= (p.Glu157=) c.2460G= (p.Glu820=) c.744G= (p.Glu248=) | |
| 2 | g.29220760C>G | CA346473050 | ALK | c.3591G>C (p.Glu1197Asp) c.818G>C n.468G>C c.387G>C (p.Glu129Asp) c.471G>C (p.Glu157Asp) c.2460G>C (p.Glu820Asp) c.744G>C (p.Glu248Asp) | dbSNP |
| 2 | g.29220760C>T | CA1593859 | ALK | c.3591G>A (p.Glu1197=) c.818G>A n.468G>A c.387G>A (p.Glu129=) c.471G>A (p.Glu157=) c.2460G>A (p.Glu820=) c.744G>A (p.Glu248=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 2 | g.29220761T>A | CA346473052 | ALK | c.3590A>T (p.Glu1197Val) c.817A>T n.467A>T c.386A>T (p.Glu129Val) c.470A>T (p.Glu157Val) c.2459A>T (p.Glu820Val) c.743A>T (p.Glu248Val) | |
| 2 | g.29220761T>C | CA346473053 | ALK | c.3590A>G (p.Glu1197Gly) c.817A>G n.467A>G c.386A>G (p.Glu129Gly) c.470A>G (p.Glu157Gly) c.2459A>G (p.Glu820Gly) c.743A>G (p.Glu248Gly) | |
| 2 | g.29220761T>G | CA346473054 | ALK | c.3590A>C (p.Glu1197Ala) c.817A>C n.467A>C c.386A>C (p.Glu129Ala) c.470A>C (p.Glu157Ala) c.2459A>C (p.Glu820Ala) c.743A>C (p.Glu248Ala) | |
| 2 | g.29220762C>A | CA346473055 | ALK | c.3589G>T (p.Glu1197Ter) c.816G>T n.466G>T c.385G>T (p.Glu129Ter) c.469G>T (p.Glu157Ter) c.2458G>T (p.Glu820Ter) c.742G>T (p.Glu248Ter) | |
| 2 | g.29220762C= | CA1241089776 | ALK | c.3589G= (p.Glu1197=) c.816G= n.466G= c.385G= (p.Glu129=) c.469G= (p.Glu157=) c.2458G= (p.Glu820=) c.742G= (p.Glu248=) | |
| 2 | g.29220762C>G | CA346473056 | ALK | c.3589G>C (p.Glu1197Gln) c.816G>C n.466G>C c.385G>C (p.Glu129Gln) c.469G>C (p.Glu157Gln) c.2458G>C (p.Glu820Gln) c.742G>C (p.Glu248Gln) | |
| 2 | g.29220762C>T | CA346473057 | ALK | c.3589G>A (p.Glu1197Lys) c.816G>A n.466G>A c.385G>A (p.Glu129Lys) c.469G>A (p.Glu157Lys) c.2458G>A (p.Glu820Lys) c.742G>A (p.Glu248Lys) | dbSNP gnomAD v2 gnomAD v4 COSMIC |
| 2 | g.29220763C>A | CA425619399 | ALK | c.3588G>T (p.Leu1196=) c.815G>T n.465G>T c.384G>T (p.Leu128=) c.468G>T (p.Leu156=) c.2457G>T (p.Leu819=) c.741G>T (p.Leu247=) | |
| 2 | g.29220763C= | CA1241089777 | ALK | c.3588G= (p.Leu1196=) c.815G= n.465G= c.384G= (p.Leu128=) c.468G= (p.Leu156=) c.2457G= (p.Leu819=) c.741G= (p.Leu247=) | |
| 2 | g.29220763C>G | CA425619398 | ALK | c.3588G>C (p.Leu1196=) c.815G>C n.465G>C c.384G>C (p.Leu128=) c.468G>C (p.Leu156=) c.2457G>C (p.Leu819=) c.741G>C (p.Leu247=) | dbSNP |
| 2 | g.29220763C>T | CA425619397 | ALK | c.3588G>A (p.Leu1196=) c.815G>A n.465G>A c.384G>A (p.Leu128=) c.468G>A (p.Leu156=) c.2457G>A (p.Leu819=) c.741G>A (p.Leu247=) | ClinVar dbSNP |
| 2 | g.29220764A= | CA1241089778 | ALK | c.3587T= (p.Leu1196=) c.814T= n.464T= c.383T= (p.Leu128=) c.467T= (p.Leu156=) c.2456T= (p.Leu819=) c.740T= (p.Leu247=) | |
| 2 | g.29220764A>C | CA346473058 | ALK | c.3587T>G (p.Leu1196Arg) c.814T>G n.464T>G c.383T>G (p.Leu128Arg) c.467T>G (p.Leu156Arg) c.2456T>G (p.Leu819Arg) c.740T>G (p.Leu247Arg) | |
| 2 | g.29220764A>G | CA346473059 | ALK | c.3587T>C (p.Leu1196Pro) c.814T>C n.464T>C c.383T>C (p.Leu128Pro) c.467T>C (p.Leu156Pro) c.2456T>C (p.Leu819Pro) c.740T>C (p.Leu247Pro) | ClinVar dbSNP |
| 2 | g.29220764A>T | CA346473060 | ALK | c.3587T>A (p.Leu1196Gln) c.814T>A n.464T>A c.383T>A (p.Leu128Gln) c.467T>A (p.Leu156Gln) c.2456T>A (p.Leu819Gln) c.740T>A (p.Leu247Gln) | dbSNP COSMIC |
| 2 | g.29220765G>A | CA425619400 | ALK | c.3586C>T (p.Leu1196=) c.813C>T n.463C>T c.382C>T (p.Leu128=) c.466C>T (p.Leu156=) c.2455C>T (p.Leu819=) c.739C>T (p.Leu247=) | ClinVar dbSNP gnomAD v4 |
| 2 | g.29220765G>C | CA346473061 | ALK | c.3586C>G (p.Leu1196Val) c.813C>G n.463C>G c.382C>G (p.Leu128Val) c.466C>G (p.Leu156Val) c.2455C>G (p.Leu819Val) c.739C>G (p.Leu247Val) | dbSNP |
| 2 | g.29220765G= | CA1241089779 | ALK | c.3586C= (p.Leu1196=) c.813C= n.463C= c.382C= (p.Leu128=) c.466C= (p.Leu156=) c.2455C= (p.Leu819=) c.739C= (p.Leu247=) | |
| 2 | g.29220765G>T | CA16602593 | ALK | c.3586C>A (p.Leu1196Met) c.813C>A n.463C>A c.382C>A (p.Leu128Met) c.466C>A (p.Leu156Met) c.2455C>A (p.Leu819Met) c.739C>A (p.Leu247Met) | ClinVar dbSNP COSMIC |
| 2 | g.29220766C>A | CA425619403 | ALK | c.3585G>T (p.Leu1195=) c.812G>T n.462G>T c.381G>T (p.Leu127=) c.465G>T (p.Leu155=) c.2454G>T (p.Leu818=) c.738G>T (p.Leu246=) | ClinVar dbSNP |
| 2 | g.29220766C>G | CA425619402 | ALK | c.3585G>C (p.Leu1195=) c.812G>C n.462G>C c.381G>C (p.Leu127=) c.465G>C (p.Leu155=) c.2454G>C (p.Leu818=) c.738G>C (p.Leu246=) | ClinVar dbSNP |
| 2 | g.29220766C>T | CA425619401 | ALK | c.3585G>A (p.Leu1195=) c.812G>A n.462G>A c.381G>A (p.Leu127=) c.465G>A (p.Leu155=) c.2454G>A (p.Leu818=) c.738G>A (p.Leu246=) | ClinVar dbSNP |
| 2 | g.29220767A>C | CA346473062 | ALK | c.3584T>G (p.Leu1195Arg) c.811T>G n.461T>G c.380T>G (p.Leu127Arg) c.464T>G (p.Leu155Arg) c.2453T>G (p.Leu818Arg) c.737T>G (p.Leu246Arg) | ClinVar gnomAD v4 |
| 2 | g.29220767A>G | CA346473063 | ALK | c.3584T>C (p.Leu1195Pro) c.811T>C n.461T>C c.380T>C (p.Leu127Pro) c.464T>C (p.Leu155Pro) c.2453T>C (p.Leu818Pro) c.737T>C (p.Leu246Pro) | dbSNP |
| 2 | g.29220767A>T | CA346473064 | ALK | c.3584T>A (p.Leu1195Gln) c.811T>A n.461T>A c.380T>A (p.Leu127Gln) c.464T>A (p.Leu155Gln) c.2453T>A (p.Leu818Gln) c.737T>A (p.Leu246Gln) | |
| 2 | g.29220768G>A | CA425619404 | ALK | c.3583C>T (p.Leu1195=) c.810C>T n.460C>T c.379C>T (p.Leu127=) c.463C>T (p.Leu155=) c.2452C>T (p.Leu818=) c.736C>T (p.Leu246=) | dbSNP |
| 2 | g.29220768G>C | CA346473065 | ALK | c.3583C>G (p.Leu1195Val) c.810C>G n.460C>G c.379C>G (p.Leu127Val) c.463C>G (p.Leu155Val) c.2452C>G (p.Leu818Val) c.736C>G (p.Leu246Val) | dbSNP gnomAD v4 |
| 2 | g.29220768G>T | CA346473066 | ALK | c.3583C>A (p.Leu1195Met) c.810C>A n.460C>A c.379C>A (p.Leu127Met) c.463C>A (p.Leu155Met) c.2452C>A (p.Leu818Met) c.736C>A (p.Leu246Met) | |
| 2 | g.29220769G>A | CA425619405 | ALK | c.3582C>T (p.Ile1194=) c.809C>T n.459C>T c.378C>T (p.Ile126=) c.462C>T (p.Ile154=) c.2451C>T (p.Ile817=) c.735C>T (p.Ile245=) | ClinVar dbSNP gnomAD v4 COSMIC |
| 2 | g.29220769G>C | CA346473067 | ALK | c.3582C>G (p.Ile1194Met) c.809C>G n.459C>G c.378C>G (p.Ile126Met) c.462C>G (p.Ile154Met) c.2451C>G (p.Ile817Met) c.735C>G (p.Ile245Met) | dbSNP |
| 2 | g.29220769G= | CA1241089780 | ALK | c.3582C= (p.Ile1194=) c.809C= n.459C= c.378C= (p.Ile126=) c.462C= (p.Ile154=) c.2451C= (p.Ile817=) c.735C= (p.Ile245=) | |
| 2 | g.29220769G>T | CA425619406 | ALK | c.3582C>A (p.Ile1194=) c.809C>A n.459C>A c.378C>A (p.Ile126=) c.462C>A (p.Ile154=) c.2451C>A (p.Ile817=) c.735C>A (p.Ile245=) | dbSNP |
| 2 | g.29220770A>C | CA346473068 | ALK | c.3581T>G (p.Ile1194Ser) c.808T>G n.458T>G c.377T>G (p.Ile126Ser) c.461T>G (p.Ile154Ser) c.2450T>G (p.Ile817Ser) c.734T>G (p.Ile245Ser) | |
| 2 | g.29220770A>G | CA346473069 | ALK | c.3581T>C (p.Ile1194Thr) c.808T>C n.458T>C c.377T>C (p.Ile126Thr) c.461T>C (p.Ile154Thr) c.2450T>C (p.Ile817Thr) c.734T>C (p.Ile245Thr) | dbSNP |
| 2 | g.29220770A>T | CA346473070 | ALK | c.3581T>A (p.Ile1194Asn) c.808T>A n.458T>A c.377T>A (p.Ile126Asn) c.461T>A (p.Ile154Asn) c.2450T>A (p.Ile817Asn) c.734T>A (p.Ile245Asn) | dbSNP |
| 2 | g.29220771T>A | CA346473071 | ALK | c.3580A>T (p.Ile1194Phe) c.807A>T n.457A>T c.376A>T (p.Ile126Phe) c.460A>T (p.Ile154Phe) c.2449A>T (p.Ile817Phe) c.733A>T (p.Ile245Phe) | dbSNP |
| 2 | g.29220771T>C | CA346473072 | ALK | c.3580A>G (p.Ile1194Val) c.807A>G n.457A>G c.376A>G (p.Ile126Val) c.460A>G (p.Ile154Val) c.2449A>G (p.Ile817Val) c.733A>G (p.Ile245Val) | |
| 2 | g.29220771T>G | CA346473073 | ALK | c.3580A>C (p.Ile1194Leu) c.807A>C n.457A>C c.376A>C (p.Ile126Leu) c.460A>C (p.Ile154Leu) c.2449A>C (p.Ile817Leu) c.733A>C (p.Ile245Leu) | |
| 2 | g.29220772G>A | CA425619407 | ALK | c.3579C>T (p.Phe1193=) c.806C>T n.456C>T c.375C>T (p.Phe125=) c.459C>T (p.Phe153=) c.2448C>T (p.Phe816=) c.732C>T (p.Phe244=) | dbSNP |
| 2 | g.29220772G>C | CA346473074 | ALK | c.3579C>G (p.Phe1193Leu) c.806C>G n.456C>G c.375C>G (p.Phe125Leu) c.459C>G (p.Phe153Leu) c.2448C>G (p.Phe816Leu) c.732C>G (p.Phe244Leu) | ClinVar dbSNP |
| 2 | g.29220772G>T | CA346473075 | ALK | c.3579C>A (p.Phe1193Leu) c.806C>A n.456C>A c.375C>A (p.Phe125Leu) c.459C>A (p.Phe153Leu) c.2448C>A (p.Phe816Leu) c.732C>A (p.Phe244Leu) | dbSNP |
| 2 | g.29220773A>C | CA346473076 | ALK | c.3578T>G (p.Phe1193Cys) c.805T>G n.455T>G c.374T>G (p.Phe125Cys) c.458T>G (p.Phe153Cys) c.2447T>G (p.Phe816Cys) c.731T>G (p.Phe244Cys) | dbSNP |
| 2 | g.29220773A>G | CA346473077 | ALK | c.3578T>C (p.Phe1193Ser) c.805T>C n.455T>C c.374T>C (p.Phe125Ser) c.458T>C (p.Phe153Ser) c.2447T>C (p.Phe816Ser) c.731T>C (p.Phe244Ser) | ClinVar dbSNP |
| 2 | g.29220773A>T | CA346473078 | ALK | c.3578T>A (p.Phe1193Tyr) c.805T>A n.455T>A c.374T>A (p.Phe125Tyr) c.458T>A (p.Phe153Tyr) c.2447T>A (p.Phe816Tyr) c.731T>A (p.Phe244Tyr) | dbSNP |
| 2 | g.29220774A>C | CA346473080 | ALK | c.3577T>G (p.Phe1193Val) c.804T>G n.454T>G c.373T>G (p.Phe125Val) c.457T>G (p.Phe153Val) c.2446T>G (p.Phe816Val) c.730T>G (p.Phe244Val) | dbSNP |
| 2 | g.29220774A>G | CA346473081 | ALK | c.3577T>C (p.Phe1193Leu) c.804T>C n.454T>C c.373T>C (p.Phe125Leu) c.457T>C (p.Phe153Leu) c.2446T>C (p.Phe816Leu) c.730T>C (p.Phe244Leu) | dbSNP |
| 2 | g.29220774A>T | CA346473079 | ALK | c.3577T>A (p.Phe1193Ile) c.804T>A n.454T>A c.373T>A (p.Phe125Ile) c.457T>A (p.Phe153Ile) c.2446T>A (p.Phe816Ile) c.730T>A (p.Phe244Ile) | dbSNP |
| 2 | g.29220775C>A | CA425619408 | ALK | c.3576G>T (p.Arg1192=) c.803G>T n.453G>T c.372G>T (p.Arg124=) c.456G>T (p.Arg152=) c.2445G>T (p.Arg815=) c.729G>T (p.Arg243=) | ClinVar dbSNP |
| 2 | g.29220775C= | CA1241089781 | ALK | c.3576G= (p.Arg1192=) c.803G= n.453G= c.372G= (p.Arg124=) c.456G= (p.Arg152=) c.2445G= (p.Arg815=) c.729G= (p.Arg243=) | |
| 2 | g.29220775C>G | CA425619409 | ALK | c.3576G>C (p.Arg1192=) c.803G>C n.453G>C c.372G>C (p.Arg124=) c.456G>C (p.Arg152=) c.2445G>C (p.Arg815=) c.729G>C (p.Arg243=) | dbSNP |
| 2 | g.29220775C>T | CA425619410 | ALK | c.3576G>A (p.Arg1192=) c.803G>A n.453G>A c.372G>A (p.Arg124=) c.456G>A (p.Arg152=) c.2445G>A (p.Arg815=) c.729G>A (p.Arg243=) | ClinVar dbSNP |
| 2 | g.29220776del | CA2658461731 | ALK | c.3576del (p.Phe1193SerfsTer?) c.803del n.453del c.372del (p.Phe125SerfsTer?) c.456del (p.Phe153SerfsTer?) c.2445del (p.Phe816SerfsTer?) c.729del (p.Phe244SerfsTer?) | gnomAD v4 |
| 2 | g.29220776C>A | CA346473082 | ALK | c.3575G>T (p.Arg1192Leu) c.802G>T n.452G>T c.371G>T (p.Arg124Leu) c.455G>T (p.Arg152Leu) c.2444G>T (p.Arg815Leu) c.728G>T (p.Arg243Leu) | gnomAD v4 |
| 2 | g.29220776C= | CA1241089782 | ALK | c.3575G= (p.Arg1192=) c.802G= n.452G= c.371G= (p.Arg124=) c.455G= (p.Arg152=) c.2444G= (p.Arg815=) c.728G= (p.Arg243=) | |
| 2 | g.29220776C>G | CA341486 | ALK | c.3575G>C (p.Arg1192Pro) c.802G>C n.452G>C c.371G>C (p.Arg124Pro) c.455G>C (p.Arg152Pro) c.2444G>C (p.Arg815Pro) c.728G>C (p.Arg243Pro) | ClinVar dbSNP |
| 2 | g.29220776C>T | CA346473083 | ALK | c.3575G>A (p.Arg1192Gln) c.802G>A n.452G>A c.371G>A (p.Arg124Gln) c.455G>A (p.Arg152Gln) c.2444G>A (p.Arg815Gln) c.728G>A (p.Arg243Gln) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 2 | g.29220777G>A | CA1593860 | ALK | c.3574C>T (p.Arg1192Trp) c.801C>T n.451C>T c.370C>T (p.Arg124Trp) c.454C>T (p.Arg152Trp) c.2443C>T (p.Arg815Trp) c.727C>T (p.Arg243Trp) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 2 | g.29220777G>C | CA44655555 | ALK | c.3574C>G (p.Arg1192Gly) c.801C>G n.451C>G c.370C>G (p.Arg124Gly) c.454C>G (p.Arg152Gly) c.2443C>G (p.Arg815Gly) c.727C>G (p.Arg243Gly) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 2 | g.29220777G= | CA1241089783 | ALK | c.3574C= (p.Arg1192=) c.801C= n.451C= c.370C= (p.Arg124=) c.454C= (p.Arg152=) c.2443C= (p.Arg815=) c.727C= (p.Arg243=) | |
| 2 | g.29220777G>T | CA425619411 | ALK | c.3574C>A (p.Arg1192=) c.801C>A n.451C>A c.370C>A (p.Arg124=) c.454C>A (p.Arg152=) c.2443C>A (p.Arg815=) c.727C>A (p.Arg243=) | ClinVar dbSNP gnomAD v4 |
| 2 | g.29220778G>A | CA425619412 | ALK | c.3573C>T (p.Pro1191=) c.800C>T n.450C>T c.369C>T (p.Pro123=) c.453C>T (p.Pro151=) c.2442C>T (p.Pro814=) c.726C>T (p.Pro242=) | ClinVar dbSNP gnomAD v4 |
| 2 | g.29220778G>C | CA425619413 | ALK | c.3573C>G (p.Pro1191=) c.800C>G n.450C>G c.369C>G (p.Pro123=) c.453C>G (p.Pro151=) c.2442C>G (p.Pro814=) c.726C>G (p.Pro242=) | dbSNP |
| 2 | g.29220778G>T | CA425619414 | ALK | c.3573C>A (p.Pro1191=) c.800C>A n.450C>A c.369C>A (p.Pro123=) c.453C>A (p.Pro151=) c.2442C>A (p.Pro814=) c.726C>A (p.Pro242=) | dbSNP COSMIC |
| 2 | g.29220779G>A | CA346473084 | ALK | c.3572C>T (p.Pro1191Leu) c.799C>T n.449C>T c.368C>T (p.Pro123Leu) c.452C>T (p.Pro151Leu) c.2441C>T (p.Pro814Leu) c.725C>T (p.Pro242Leu) | dbSNP COSMIC |
| 2 | g.29220779G>C | CA346473085 | ALK | c.3572C>G (p.Pro1191Arg) c.799C>G n.449C>G c.368C>G (p.Pro123Arg) c.452C>G (p.Pro151Arg) c.2441C>G (p.Pro814Arg) c.725C>G (p.Pro242Arg) | dbSNP |
| 2 | g.29220779G= | CA1241089784 | ALK | c.3572C= (p.Pro1191=) c.799C= n.449C= c.368C= (p.Pro123=) c.452C= (p.Pro151=) c.2441C= (p.Pro814=) c.725C= (p.Pro242=) | |
| 2 | g.29220779G>T | CA16610701 | ALK | c.3572C>A (p.Pro1191His) c.799C>A n.449C>A c.368C>A (p.Pro123His) c.452C>A (p.Pro151His) c.2441C>A (p.Pro814His) c.725C>A (p.Pro242His) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 2 | g.29220780G>A | CA346473086 | ALK | c.3571C>T (p.Pro1191Ser) c.798C>T n.448C>T c.367C>T (p.Pro123Ser) c.451C>T (p.Pro151Ser) c.2440C>T (p.Pro814Ser) c.724C>T (p.Pro242Ser) | dbSNP gnomAD v4 COSMIC |
| 2 | g.29220780G>C | CA346473087 | ALK | c.3571C>G (p.Pro1191Ala) c.798C>G n.448C>G c.367C>G (p.Pro123Ala) c.451C>G (p.Pro151Ala) c.2440C>G (p.Pro814Ala) c.724C>G (p.Pro242Ala) | dbSNP |
| 2 | g.29220780G>T | CA346473088 | ALK | c.3571C>A (p.Pro1191Thr) c.798C>A n.448C>A c.367C>A (p.Pro123Thr) c.451C>A (p.Pro151Thr) c.2440C>A (p.Pro814Thr) c.724C>A (p.Pro242Thr) | ClinVar dbSNP |
| 2 | g.29220781C>A | CA425619415 | ALK | c.3570G>T (p.Leu1190=) c.797G>T n.447G>T c.366G>T (p.Leu122=) c.450G>T (p.Leu150=) c.2439G>T (p.Leu813=) c.723G>T (p.Leu241=) | ClinVar |
| 2 | g.29220781C= | CA1241089785 | ALK | c.3570G= (p.Leu1190=) c.797G= n.447G= c.366G= (p.Leu122=) c.450G= (p.Leu150=) c.2439G= (p.Leu813=) c.723G= (p.Leu241=) | |
| 2 | g.29220781C>G | CA425619416 | ALK | c.3570G>C (p.Leu1190=) c.797G>C n.447G>C c.366G>C (p.Leu122=) c.450G>C (p.Leu150=) c.2439G>C (p.Leu813=) c.723G>C (p.Leu241=) | dbSNP |
| 2 | g.29220781C>T | CA425619417 | ALK | c.3570G>A (p.Leu1190=) c.797G>A n.447G>A c.366G>A (p.Leu122=) c.450G>A (p.Leu150=) c.2439G>A (p.Leu813=) c.723G>A (p.Leu241=) | dbSNP |
| 2 | g.29220782A= | CA1241089786 | ALK | c.3569T= (p.Leu1190=) c.796T= n.446T= c.365T= (p.Leu122=) c.449T= (p.Leu150=) c.2438T= (p.Leu813=) c.722T= (p.Leu241=) | |
| 2 | g.29220782A>C | CA346473089 | ALK | c.3569T>G (p.Leu1190Arg) c.796T>G n.446T>G c.365T>G (p.Leu122Arg) c.449T>G (p.Leu150Arg) c.2438T>G (p.Leu813Arg) c.722T>G (p.Leu241Arg) | |
| 2 | g.29220782A>G | CA346473090 | ALK | c.3569T>C (p.Leu1190Pro) c.796T>C n.446T>C c.365T>C (p.Leu122Pro) c.449T>C (p.Leu150Pro) c.2438T>C (p.Leu813Pro) c.722T>C (p.Leu241Pro) | ClinVar dbSNP |
| 2 | g.29220782A>T | CA346473091 | ALK | c.3569T>A (p.Leu1190Gln) c.796T>A n.446T>A c.365T>A (p.Leu122Gln) c.449T>A (p.Leu150Gln) c.2438T>A (p.Leu813Gln) c.722T>A (p.Leu241Gln) | |
| 2 | g.29220783G>A | CA425619418 | ALK | c.3568C>T (p.Leu1190=) c.795C>T n.445C>T c.364C>T (p.Leu122=) c.448C>T (p.Leu150=) c.2437C>T (p.Leu813=) c.721C>T (p.Leu241=) | dbSNP |
| 2 | g.29220783G>C | CA346473092 | ALK | c.3568C>G (p.Leu1190Val) c.795C>G n.445C>G c.364C>G (p.Leu122Val) c.448C>G (p.Leu150Val) c.2437C>G (p.Leu813Val) c.721C>G (p.Leu241Val) | dbSNP gnomAD v4 |
| 2 | g.29220783G= | CA1241089787 | ALK | c.3568C= (p.Leu1190=) c.795C= n.445C= c.364C= (p.Leu122=) c.448C= (p.Leu150=) c.2437C= (p.Leu813=) c.721C= (p.Leu241=) | |
| 2 | g.29220783G>T | CA1593861 | ALK | c.3568C>A (p.Leu1190Met) c.795C>A n.445C>A c.364C>A (p.Leu122Met) c.448C>A (p.Leu150Met) c.2437C>A (p.Leu813Met) c.721C>A (p.Leu241Met) | dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC |
| 2 | g.29220784G>A | CA425619421 | ALK | c.3567C>T (p.Ser1189=) c.794C>T n.444C>T c.363C>T (p.Ser121=) c.447C>T (p.Ser149=) c.2436C>T (p.Ser812=) c.720C>T (p.Ser240=) | ClinVar gnomAD v4 |
| 2 | g.29220784G>C | CA425619420 | ALK | c.3567C>G (p.Ser1189=) c.794C>G n.444C>G c.363C>G (p.Ser121=) c.447C>G (p.Ser149=) c.2436C>G (p.Ser812=) c.720C>G (p.Ser240=) | ClinVar |
| 2 | g.29220784G>T | CA425619419 | ALK | c.3567C>A (p.Ser1189=) c.794C>A n.444C>A c.363C>A (p.Ser121=) c.447C>A (p.Ser149=) c.2436C>A (p.Ser812=) c.720C>A (p.Ser240=) | dbSNP |
| 2 | g.29220785G>A | CA346473094 | ALK | c.3566C>T (p.Ser1189Phe) c.793C>T n.443C>T c.362C>T (p.Ser121Phe) c.446C>T (p.Ser149Phe) c.2435C>T (p.Ser812Phe) c.719C>T (p.Ser240Phe) | dbSNP COSMIC |
| 2 | g.29220785G>C | CA346473093 | ALK | c.3566C>G (p.Ser1189Cys) c.793C>G n.443C>G c.362C>G (p.Ser121Cys) c.446C>G (p.Ser149Cys) c.2435C>G (p.Ser812Cys) c.719C>G (p.Ser240Cys) | dbSNP gnomAD v4 |
| 2 | g.29220785G= | CA1241089788 | ALK | c.3566C= (p.Ser1189=) c.793C= n.443C= c.362C= (p.Ser121=) c.446C= (p.Ser149=) c.2435C= (p.Ser812=) c.719C= (p.Ser240=) | |
| 2 | g.29220785G>T | CA44655575 | ALK | c.3566C>A (p.Ser1189Tyr) c.793C>A n.443C>A c.362C>A (p.Ser121Tyr) c.446C>A (p.Ser149Tyr) c.2435C>A (p.Ser812Tyr) c.719C>A (p.Ser240Tyr) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 2 | g.29220786A>C | CA346473095 | ALK | c.3565T>G (p.Ser1189Ala) c.792T>G n.442T>G c.361T>G (p.Ser121Ala) c.445T>G (p.Ser149Ala) c.2434T>G (p.Ser812Ala) c.718T>G (p.Ser240Ala) | dbSNP |
| 2 | g.29220786A>G | CA346473096 | ALK | c.3565T>C (p.Ser1189Pro) c.792T>C n.442T>C c.361T>C (p.Ser121Pro) c.445T>C (p.Ser149Pro) c.2434T>C (p.Ser812Pro) c.718T>C (p.Ser240Pro) | |
| 2 | g.29220786A>T | CA346473097 | ALK | c.3565T>A (p.Ser1189Thr) c.792T>A n.442T>A c.361T>A (p.Ser121Thr) c.445T>A (p.Ser149Thr) c.2434T>A (p.Ser812Thr) c.718T>A (p.Ser240Thr) | dbSNP |
| 2 | g.29220787T>A | CA346473098 | ALK | c.3564A>T (p.Gln1188His) c.791A>T n.441A>T c.360A>T (p.Gln120His) c.444A>T (p.Gln148His) c.2433A>T (p.Gln811His) c.717A>T (p.Gln239His) | dbSNP gnomAD v4 |
| 2 | g.29220787T>C | CA425619422 | ALK | c.3564A>G (p.Gln1188=) c.791A>G n.441A>G c.360A>G (p.Gln120=) c.444A>G (p.Gln148=) c.2433A>G (p.Gln811=) c.717A>G (p.Gln239=) | ClinVar dbSNP |
| 2 | g.29220787T>G | CA346473099 | ALK | c.3564A>C (p.Gln1188His) c.791A>C n.441A>C c.360A>C (p.Gln120His) c.444A>C (p.Gln148His) c.2433A>C (p.Gln811His) c.717A>C (p.Gln239His) | dbSNP |
| 2 | g.29220788T>A | CA346473100 | ALK | c.3563A>T (p.Gln1188Leu) c.790A>T n.440A>T c.359A>T (p.Gln120Leu) c.443A>T (p.Gln148Leu) c.2432A>T (p.Gln811Leu) c.716A>T (p.Gln239Leu) | |
| 2 | g.29220788T>C | CA346473101 | ALK | c.3563A>G (p.Gln1188Arg) c.790A>G n.440A>G c.359A>G (p.Gln120Arg) c.443A>G (p.Gln148Arg) c.2432A>G (p.Gln811Arg) c.716A>G (p.Gln239Arg) | ClinVar dbSNP gnomAD v4 |
| 2 | g.29220788T>G | CA346473102 | ALK | c.3563A>C (p.Gln1188Pro) c.790A>C n.440A>C c.359A>C (p.Gln120Pro) c.443A>C (p.Gln148Pro) c.2432A>C (p.Gln811Pro) c.716A>C (p.Gln239Pro) | |
| 2 | g.29220788T= | CA1241089789 | ALK | c.3563A= (p.Gln1188=) c.790A= n.440A= c.359A= (p.Gln120=) c.443A= (p.Gln148=) c.2432A= (p.Gln811=) c.716A= (p.Gln239=) | |
| 2 | g.29220789G>A | CA346473103 | ALK | c.3562C>T (p.Gln1188Ter) c.789C>T n.439C>T c.358C>T (p.Gln120Ter) c.442C>T (p.Gln148Ter) c.2431C>T (p.Gln811Ter) c.715C>T (p.Gln239Ter) | ClinVar dbSNP |
| 2 | g.29220789G>C | CA346473104 | ALK | c.3562C>G (p.Gln1188Glu) c.789C>G n.439C>G c.358C>G (p.Gln120Glu) c.442C>G (p.Gln148Glu) c.2431C>G (p.Gln811Glu) c.715C>G (p.Gln239Glu) | dbSNP |
| 2 | g.29220789G= | CA1241089790 | ALK | c.3562C= (p.Gln1188=) c.789C= n.439C= c.358C= (p.Gln120=) c.442C= (p.Gln148=) c.2431C= (p.Gln811=) c.715C= (p.Gln239=) | |
| 2 | g.29220789G>T | CA346473105 | ALK | c.3562C>A (p.Gln1188Lys) c.789C>A n.439C>A c.358C>A (p.Gln120Lys) c.442C>A (p.Gln148Lys) c.2431C>A (p.Gln811Lys) c.715C>A (p.Gln239Lys) | dbSNP |
| 2 | g.29220790C>A | CA425619423 | ALK | c.3561G>T (p.Leu1187=) c.788G>T n.438G>T c.357G>T (p.Leu119=) c.441G>T (p.Leu147=) c.2430G>T (p.Leu810=) c.714G>T (p.Leu238=) | dbSNP |
| 2 | g.29220790C>G | CA425619424 | ALK | c.3561G>C (p.Leu1187=) c.788G>C n.438G>C c.357G>C (p.Leu119=) c.441G>C (p.Leu147=) c.2430G>C (p.Leu810=) c.714G>C (p.Leu238=) | dbSNP |
| 2 | g.29220790C>T | CA425619425 | ALK | c.3561G>A (p.Leu1187=) c.788G>A n.438G>A c.357G>A (p.Leu119=) c.441G>A (p.Leu147=) c.2430G>A (p.Leu810=) c.714G>A (p.Leu238=) | dbSNP |
| 2 | g.29220791A>C | CA346473108 | ALK | c.3560T>G (p.Leu1187Arg) c.787T>G n.437T>G c.356T>G (p.Leu119Arg) c.440T>G (p.Leu147Arg) c.2429T>G (p.Leu810Arg) c.713T>G (p.Leu238Arg) | |
| 2 | g.29220791A>G | CA346473107 | ALK | c.3560T>C (p.Leu1187Pro) c.787T>C n.437T>C c.356T>C (p.Leu119Pro) c.440T>C (p.Leu147Pro) c.2429T>C (p.Leu810Pro) c.713T>C (p.Leu238Pro) | dbSNP |
| 2 | g.29220791A>T | CA346473106 | ALK | c.3560T>A (p.Leu1187Gln) c.787T>A n.437T>A c.356T>A (p.Leu119Gln) c.440T>A (p.Leu147Gln) c.2429T>A (p.Leu810Gln) c.713T>A (p.Leu238Gln) | dbSNP |
| 2 | g.29220792G>A | CA425619426 | ALK | c.3559C>T (p.Leu1187=) c.786C>T n.436C>T c.355C>T (p.Leu119=) c.439C>T (p.Leu147=) c.2428C>T (p.Leu810=) c.712C>T (p.Leu238=) | gnomAD v4 |
| 2 | g.29220792G>C | CA346473109 | ALK | c.3559C>G (p.Leu1187Val) c.786C>G n.436C>G c.355C>G (p.Leu119Val) c.439C>G (p.Leu147Val) c.2428C>G (p.Leu810Val) c.712C>G (p.Leu238Val) | |
| 2 | g.29220792G>T | CA346473110 | ALK | c.3559C>A (p.Leu1187Met) c.786C>A n.436C>A c.355C>A (p.Leu119Met) c.439C>A (p.Leu147Met) c.2428C>A (p.Leu810Met) c.712C>A (p.Leu238Met) | |
| 2 | g.29220793G>A | CA425619427 | ALK | c.3558C>T (p.Ser1186=) c.785C>T n.435C>T c.354C>T (p.Ser118=) c.438C>T (p.Ser146=) c.2427C>T (p.Ser809=) c.711C>T (p.Ser237=) | dbSNP |
| 2 | g.29220793G>C | CA346473111 | ALK | c.3558C>G (p.Ser1186Arg) c.785C>G n.435C>G c.354C>G (p.Ser118Arg) c.438C>G (p.Ser146Arg) c.2427C>G (p.Ser809Arg) c.711C>G (p.Ser237Arg) | dbSNP |
| 2 | g.29220793G>T | CA346473112 | ALK | c.3558C>A (p.Ser1186Arg) c.785C>A n.435C>A c.354C>A (p.Ser118Arg) c.438C>A (p.Ser146Arg) c.2427C>A (p.Ser809Arg) c.711C>A (p.Ser237Arg) | |
| 2 | g.29220794C>A | CA346473113 | ALK | c.3557G>T (p.Ser1186Ile) c.784G>T n.434G>T c.353G>T (p.Ser118Ile) c.437G>T (p.Ser146Ile) c.2426G>T (p.Ser809Ile) c.710G>T (p.Ser237Ile) | dbSNP |
| 2 | g.29220794C= | CA1241089791 | ALK | c.3557G= (p.Ser1186=) c.784G= n.434G= c.353G= (p.Ser118=) c.437G= (p.Ser146=) c.2426G= (p.Ser809=) c.710G= (p.Ser237=) | |
| 2 | g.29220794C>G | CA346473114 | ALK | c.3557G>C (p.Ser1186Thr) c.784G>C n.434G>C c.353G>C (p.Ser118Thr) c.437G>C (p.Ser146Thr) c.2426G>C (p.Ser809Thr) c.710G>C (p.Ser237Thr) | dbSNP |
| 2 | g.29220794C>T | CA1593862 | ALK | c.3557G>A (p.Ser1186Asn) c.784G>A n.434G>A c.353G>A (p.Ser118Asn) c.437G>A (p.Ser146Asn) c.2426G>A (p.Ser809Asn) c.710G>A (p.Ser237Asn) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 2 | g.29220795T>A | CA346473115 | ALK | c.3556A>T (p.Ser1186Cys) c.783A>T n.433A>T c.352A>T (p.Ser118Cys) c.436A>T (p.Ser146Cys) c.2425A>T (p.Ser809Cys) c.709A>T (p.Ser237Cys) | dbSNP |
| 2 | g.29220795T>C | CA346473117 | ALK | c.3556A>G (p.Ser1186Gly) c.783A>G n.433A>G c.352A>G (p.Ser118Gly) c.436A>G (p.Ser146Gly) c.2425A>G (p.Ser809Gly) c.709A>G (p.Ser237Gly) | dbSNP |
| 2 | g.29220795T>G | CA346473116 | ALK | c.3556A>C (p.Ser1186Arg) c.783A>C n.433A>C c.352A>C (p.Ser118Arg) c.436A>C (p.Ser146Arg) c.2425A>C (p.Ser809Arg) c.709A>C (p.Ser237Arg) | |
| 2 | g.29220796C>A | CA425619428 | ALK | c.3555G>T (p.Val1185=) c.782G>T n.432G>T c.351G>T (p.Val117=) c.435G>T (p.Val145=) c.2424G>T (p.Val808=) c.708G>T (p.Val236=) | ClinVar dbSNP gnomAD v4 |
| 2 | g.29220796C= | CA1241089792 | ALK | c.3555G= (p.Val1185=) c.782G= n.432G= c.351G= (p.Val117=) c.435G= (p.Val145=) c.2424G= (p.Val808=) c.708G= (p.Val236=) | |
| 2 | g.29220796C>G | CA425619429 | ALK | c.3555G>C (p.Val1185=) c.782G>C n.432G>C c.351G>C (p.Val117=) c.435G>C (p.Val145=) c.2424G>C (p.Val808=) c.708G>C (p.Val236=) | dbSNP gnomAD v2 gnomAD v4 |
| 2 | g.29220796C>T | CA1593863 | ALK | c.3555G>A (p.Val1185=) c.782G>A n.432G>A c.351G>A (p.Val117=) c.435G>A (p.Val145=) c.2424G>A (p.Val808=) c.708G>A (p.Val236=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 2 | g.29220797A>C | CA346473118 | ALK | c.3554T>G (p.Val1185Gly) c.781T>G n.431T>G c.350T>G (p.Val117Gly) c.434T>G (p.Val145Gly) c.2423T>G (p.Val808Gly) c.707T>G (p.Val236Gly) | |
| 2 | g.29220797A>G | CA346473119 | ALK | c.3554T>C (p.Val1185Ala) c.781T>C n.431T>C c.350T>C (p.Val117Ala) c.434T>C (p.Val145Ala) c.2423T>C (p.Val808Ala) c.707T>C (p.Val236Ala) | gnomAD v4 |
| 2 | g.29220797A>T | CA346473120 | ALK | c.3554T>A (p.Val1185Glu) c.781T>A n.431T>A c.350T>A (p.Val117Glu) c.434T>A (p.Val145Glu) c.2423T>A (p.Val808Glu) c.707T>A (p.Val236Glu) | |
| 2 | g.29220798C>A | CA1593864 | ALK | c.3553G>T (p.Val1185Leu) c.780G>T n.430G>T c.349G>T (p.Val117Leu) c.433G>T (p.Val145Leu) c.2422G>T (p.Val808Leu) c.706G>T (p.Val236Leu) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 2 | g.29220798C= | CA1241089793 | ALK | c.3553G= (p.Val1185=) c.780G= n.430G= c.349G= (p.Val117=) c.433G= (p.Val145=) c.2422G= (p.Val808=) c.706G= (p.Val236=) | |
| 2 | g.29220798C>G | CA346473122 | ALK | c.3553G>C (p.Val1185Leu) c.780G>C n.430G>C c.349G>C (p.Val117Leu) c.433G>C (p.Val145Leu) c.2422G>C (p.Val808Leu) c.706G>C (p.Val236Leu) | dbSNP |
| 2 | g.29220798C>T | CA346473121 | ALK | c.3553G>A (p.Val1185Met) c.780G>A n.430G>A c.349G>A (p.Val117Met) c.433G>A (p.Val145Met) c.2422G>A (p.Val808Met) c.706G>A (p.Val236Met) | dbSNP |
| 2 | g.29220801del | CA2580066338 | ALK | c.3553del (p.Val1185Ter) c.780del n.430del c.349del (p.Val117Ter) c.433del (p.Val145Ter) c.2422del (p.Val808Ter) c.706del (p.Val236Ter) | ClinVar |
| 2 | g.29220799C>A | CA425619430 | ALK | c.3552G>T (p.Gly1184=) c.779G>T n.429G>T c.348G>T (p.Gly116=) c.432G>T (p.Gly144=) c.2421G>T (p.Gly807=) c.705G>T (p.Gly235=) | dbSNP |
| 2 | g.29220799C= | CA1241089794 | ALK | c.3552G= (p.Gly1184=) c.779G= n.429G= c.348G= (p.Gly116=) c.432G= (p.Gly144=) c.2421G= (p.Gly807=) c.705G= (p.Gly235=) | |
| 2 | g.29220799C>G | CA10581962 | ALK | c.3552G>C (p.Gly1184=) c.779G>C n.429G>C c.348G>C (p.Gly116=) c.432G>C (p.Gly144=) c.2421G>C (p.Gly807=) c.705G>C (p.Gly235=) | ClinVar dbSNP gnomAD v4 |
| 2 | g.29220799C>T | CA425619431 | ALK | c.3552G>A (p.Gly1184=) c.779G>A n.429G>A c.348G>A (p.Gly116=) c.432G>A (p.Gly144=) c.2421G>A (p.Gly807=) c.705G>A (p.Gly235=) | ClinVar dbSNP |
| 2 | g.29220800C>A | CA346473123 | ALK | c.3551G>T (p.Gly1184Val) c.778G>T n.428G>T c.347G>T (p.Gly116Val) c.431G>T (p.Gly144Val) c.2420G>T (p.Gly807Val) c.704G>T (p.Gly235Val) | dbSNP COSMIC |
| 2 | g.29220800C>G | CA346473124 | ALK | c.3551G>C (p.Gly1184Ala) c.778G>C n.428G>C c.347G>C (p.Gly116Ala) c.431G>C (p.Gly144Ala) c.2420G>C (p.Gly807Ala) c.704G>C (p.Gly235Ala) | dbSNP |
| 2 | g.29220800C>T | CA346473125 | ALK | c.3551G>A (p.Gly1184Glu) c.778G>A n.428G>A c.347G>A (p.Gly116Glu) c.431G>A (p.Gly144Glu) c.2420G>A (p.Gly807Glu) c.704G>A (p.Gly235Glu) | dbSNP COSMIC |
| 2 | g.29220801C>A | CA346473126 | ALK | c.3550G>T (p.Gly1184Trp) c.777G>T n.427G>T c.346G>T (p.Gly116Trp) c.430G>T (p.Gly144Trp) c.2419G>T (p.Gly807Trp) c.703G>T (p.Gly235Trp) | dbSNP |
| 2 | g.29220801C>G | CA346473127 | ALK | c.3550G>C (p.Gly1184Arg) c.777G>C n.427G>C c.346G>C (p.Gly116Arg) c.430G>C (p.Gly144Arg) c.2419G>C (p.Gly807Arg) c.703G>C (p.Gly235Arg) | dbSNP |
| 2 | g.29220801C>T | CA346473128 | ALK | c.3550G>A (p.Gly1184Arg) c.777G>A n.427G>A c.346G>A (p.Gly116Arg) c.430G>A (p.Gly144Arg) c.2419G>A (p.Gly807Arg) c.703G>A (p.Gly235Arg) | dbSNP |
| 2 | g.29220802A= | CA1241089795 | ALK | c.3549T= (p.Ile1183=) c.776T= n.426T= c.345T= (p.Ile115=) c.429T= (p.Ile143=) c.2418T= (p.Ile806=) c.702T= (p.Ile234=) | |
| 2 | g.29220802A>C | CA346473129 | ALK | c.3549T>G (p.Ile1183Met) c.776T>G n.426T>G c.345T>G (p.Ile115Met) c.429T>G (p.Ile143Met) c.2418T>G (p.Ile806Met) c.702T>G (p.Ile234Met) | ClinVar dbSNP gnomAD v4 |
| 2 | g.29220802A>G | CA425619432 | ALK | c.3549T>C (p.Ile1183=) c.776T>C n.426T>C c.345T>C (p.Ile115=) c.429T>C (p.Ile143=) c.2418T>C (p.Ile806=) c.702T>C (p.Ile234=) | |
| 2 | g.29220802A>T | CA425619433 | ALK | c.3549T>A (p.Ile1183=) c.776T>A n.426T>A c.345T>A (p.Ile115=) c.429T>A (p.Ile143=) c.2418T>A (p.Ile806=) c.702T>A (p.Ile234=) | dbSNP |
| 2 | g.29220803A= | CA1241089796 | ALK | c.3548T= (p.Ile1183=) c.775T= n.425T= c.344T= (p.Ile115=) c.428T= (p.Ile143=) c.2417T= (p.Ile806=) c.701T= (p.Ile234=) | |
| 2 | g.29220803A>C | CA346473130 | ALK | c.3548T>G (p.Ile1183Ser) c.775T>G n.425T>G c.344T>G (p.Ile115Ser) c.428T>G (p.Ile143Ser) c.2417T>G (p.Ile806Ser) c.701T>G (p.Ile234Ser) | dbSNP |
| 2 | g.29220803A>G | CA44655597 | ALK | c.3548T>C (p.Ile1183Thr) c.775T>C n.425T>C c.344T>C (p.Ile115Thr) c.428T>C (p.Ile143Thr) c.2417T>C (p.Ile806Thr) c.701T>C (p.Ile234Thr) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 2 | g.29220803A>T | CA346473131 | ALK | c.3548T>A (p.Ile1183Asn) c.775T>A n.425T>A c.344T>A (p.Ile115Asn) c.428T>A (p.Ile143Asn) c.2417T>A (p.Ile806Asn) c.701T>A (p.Ile234Asn) | dbSNP |
| 2 | g.29220804T>A | CA346473133 | ALK | c.3547A>T (p.Ile1183Phe) c.774A>T n.424A>T c.343A>T (p.Ile115Phe) c.427A>T (p.Ile143Phe) c.2416A>T (p.Ile806Phe) c.700A>T (p.Ile234Phe) | dbSNP |
| 2 | g.29220804T>C | CA1593865 | ALK | c.3547A>G (p.Ile1183Val) c.774A>G n.424A>G c.343A>G (p.Ile115Val) c.427A>G (p.Ile143Val) c.2416A>G (p.Ile806Val) c.700A>G (p.Ile234Val) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 2 | g.29220804T>G | CA346473132 | ALK | c.3547A>C (p.Ile1183Leu) c.774A>C n.424A>C c.343A>C (p.Ile115Leu) c.427A>C (p.Ile143Leu) c.2416A>C (p.Ile806Leu) c.700A>C (p.Ile234Leu) | |
| 2 | g.29220804T= | CA1241089797 | ALK | c.3547A= (p.Ile1183=) c.774A= n.424A= c.343A= (p.Ile115=) c.427A= (p.Ile143=) c.2416A= (p.Ile806=) c.700A= (p.Ile234=) | |
| 2 | g.29220805G>A | CA425619434 | ALK | c.3546C>T (p.Cys1182=) c.773C>T n.423C>T c.342C>T (p.Cys114=) c.426C>T (p.Cys142=) c.2415C>T (p.Cys805=) c.699C>T (p.Cys233=) | dbSNP gnomAD v4 |
| 2 | g.29220805G>C | CA346473134 | ALK | c.3546C>G (p.Cys1182Trp) c.773C>G n.423C>G c.342C>G (p.Cys114Trp) c.426C>G (p.Cys142Trp) c.2415C>G (p.Cys805Trp) c.699C>G (p.Cys233Trp) | dbSNP |
| 2 | g.29220805G>T | CA346473135 | ALK | c.3546C>A (p.Cys1182Ter) c.773C>A n.423C>A c.342C>A (p.Cys114Ter) c.426C>A (p.Cys142Ter) c.2415C>A (p.Cys805Ter) c.699C>A (p.Cys233Ter) | dbSNP COSMIC |
| 2 | g.29220806C>A | CA346473136 | ALK | c.3545G>T (p.Cys1182Phe) c.772G>T n.422G>T c.341G>T (p.Cys114Phe) c.425G>T (p.Cys142Phe) c.2414G>T (p.Cys805Phe) c.698G>T (p.Cys233Phe) | dbSNP |
| 2 | g.29220806C>G | CA346473137 | ALK | c.3545G>C (p.Cys1182Ser) c.772G>C n.422G>C c.341G>C (p.Cys114Ser) c.425G>C (p.Cys142Ser) c.2414G>C (p.Cys805Ser) c.698G>C (p.Cys233Ser) | dbSNP |
| 2 | g.29220806C>T | CA346473138 | ALK | c.3545G>A (p.Cys1182Tyr) c.772G>A n.422G>A c.341G>A (p.Cys114Tyr) c.425G>A (p.Cys142Tyr) c.2414G>A (p.Cys805Tyr) c.698G>A (p.Cys233Tyr) | ClinVar dbSNP |
| 2 | g.29220807A>C | CA346473139 | ALK | c.3544T>G (p.Cys1182Gly) c.771T>G n.421T>G c.340T>G (p.Cys114Gly) c.424T>G (p.Cys142Gly) c.2413T>G (p.Cys805Gly) c.697T>G (p.Cys233Gly) | gnomAD v4 |
| 2 | g.29220807A>G | CA346473140 | ALK | c.3544T>C (p.Cys1182Arg) c.771T>C n.421T>C c.340T>C (p.Cys114Arg) c.424T>C (p.Cys142Arg) c.2413T>C (p.Cys805Arg) c.697T>C (p.Cys233Arg) | dbSNP |
| 2 | g.29220807A>T | CA346473141 | ALK | c.3544T>A (p.Cys1182Ser) c.771T>A n.421T>A c.340T>A (p.Cys114Ser) c.424T>A (p.Cys142Ser) c.2413T>A (p.Cys805Ser) c.697T>A (p.Cys233Ser) | dbSNP |
| 2 | g.29220808G>A | CA425619435 | ALK | c.3543C>T (p.Arg1181=) c.770C>T n.420C>T c.339C>T (p.Arg113=) c.423C>T (p.Arg141=) c.2412C>T (p.Arg804=) c.696C>T (p.Arg232=) | dbSNP |
| 2 | g.29220808G>C | CA425619436 | ALK | c.3543C>G (p.Arg1181=) c.770C>G n.420C>G c.339C>G (p.Arg113=) c.423C>G (p.Arg141=) c.2412C>G (p.Arg804=) c.696C>G (p.Arg232=) | dbSNP |
| 2 | g.29220808G>T | CA425619437 | ALK | c.3543C>A (p.Arg1181=) c.770C>A n.420C>A c.339C>A (p.Arg113=) c.423C>A (p.Arg141=) c.2412C>A (p.Arg804=) c.696C>A (p.Arg232=) | dbSNP |
| 2 | g.29220809C>A | CA346473142 | ALK | c.3542G>T (p.Arg1181Leu) c.769G>T n.419G>T c.338G>T (p.Arg113Leu) c.422G>T (p.Arg141Leu) c.2411G>T (p.Arg804Leu) c.695G>T (p.Arg232Leu) | dbSNP |
| 2 | g.29220809C= | CA1241089798 | ALK | c.3542G= (p.Arg1181=) c.769G= n.419G= c.338G= (p.Arg113=) c.422G= (p.Arg141=) c.2411G= (p.Arg804=) c.695G= (p.Arg232=) | |
| 2 | g.29220809C>G | CA346473143 | ALK | c.3542G>C (p.Arg1181Pro) c.769G>C n.419G>C c.338G>C (p.Arg113Pro) c.422G>C (p.Arg141Pro) c.2411G>C (p.Arg804Pro) c.695G>C (p.Arg232Pro) | dbSNP gnomAD v2 |
| 2 | g.29220809C>T | CA44655607 | ALK | c.3542G>A (p.Arg1181His) c.769G>A n.419G>A c.338G>A (p.Arg113His) c.422G>A (p.Arg141His) c.2411G>A (p.Arg804His) c.695G>A (p.Arg232His) | ClinVar dbSNP gnomAD v2 gnomAD v4 COSMIC |
| 2 | g.29220810G>A | CA1593866 | ALK | c.3541C>T (p.Arg1181Cys) c.768C>T n.418C>T c.337C>T (p.Arg113Cys) c.421C>T (p.Arg141Cys) c.2410C>T (p.Arg804Cys) c.694C>T (p.Arg232Cys) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 2 | g.29220810G>C | CA346473144 | ALK | c.3541C>G (p.Arg1181Gly) c.768C>G n.418C>G c.337C>G (p.Arg113Gly) c.421C>G (p.Arg141Gly) c.2410C>G (p.Arg804Gly) c.694C>G (p.Arg232Gly) | dbSNP |
| 2 | g.29220810G= | CA1241089799 | ALK | c.3541C= (p.Arg1181=) c.768C= n.418C= c.337C= (p.Arg113=) c.421C= (p.Arg141=) c.2410C= (p.Arg804=) c.694C= (p.Arg232=) | |
| 2 | g.29220810G>T | CA346473145 | ALK | c.3541C>A (p.Arg1181Ser) c.768C>A n.418C>A c.337C>A (p.Arg113Ser) c.421C>A (p.Arg141Ser) c.2410C>A (p.Arg804Ser) c.694C>A (p.Arg232Ser) | gnomAD v4 |
| 2 | g.29220811A>C | CA425619438 | ALK | c.3540T>G (p.Val1180=) c.767T>G n.417T>G c.336T>G (p.Val112=) c.420T>G (p.Val140=) c.2409T>G (p.Val803=) c.693T>G (p.Val231=) | ClinVar dbSNP |
| 2 | g.29220811A>G | CA425619439 | ALK | c.3540T>C (p.Val1180=) c.767T>C n.417T>C c.336T>C (p.Val112=) c.420T>C (p.Val140=) c.2409T>C (p.Val803=) c.693T>C (p.Val231=) | ClinVar dbSNP |
| 2 | g.29220811A>T | CA425619440 | ALK | c.3540T>A (p.Val1180=) c.767T>A n.417T>A c.336T>A (p.Val112=) c.420T>A (p.Val140=) c.2409T>A (p.Val803=) c.693T>A (p.Val231=) | dbSNP |
| 2 | g.29220812A>C | CA346473148 | ALK | c.3539T>G (p.Val1180Gly) c.766T>G n.416T>G c.335T>G (p.Val112Gly) c.419T>G (p.Val140Gly) c.2408T>G (p.Val803Gly) c.692T>G (p.Val231Gly) | dbSNP |
| 2 | g.29220812A>G | CA346473147 | ALK | c.3539T>C (p.Val1180Ala) c.766T>C n.416T>C c.335T>C (p.Val112Ala) c.419T>C (p.Val140Ala) c.2408T>C (p.Val803Ala) c.692T>C (p.Val231Ala) | dbSNP |
| 2 | g.29220812A>T | CA346473146 | ALK | c.3539T>A (p.Val1180Asp) c.766T>A n.416T>A c.335T>A (p.Val112Asp) c.419T>A (p.Val140Asp) c.2408T>A (p.Val803Asp) c.692T>A (p.Val231Asp) | dbSNP |
| 2 | g.29220813C>A | CA346473149 | ALK | c.3538G>T (p.Val1180Phe) c.765G>T n.415G>T c.334G>T (p.Val112Phe) c.418G>T (p.Val140Phe) c.2407G>T (p.Val803Phe) c.691G>T (p.Val231Phe) | dbSNP |
| 2 | g.29220813C>G | CA346473150 | ALK | c.3538G>C (p.Val1180Leu) c.765G>C n.415G>C c.334G>C (p.Val112Leu) c.418G>C (p.Val140Leu) c.2407G>C (p.Val803Leu) c.691G>C (p.Val231Leu) | ClinVar dbSNP gnomAD v4 COSMIC |
| 2 | g.29220813C>T | CA346473151 | ALK | c.3538G>A (p.Val1180Ile) c.765G>A n.415G>A c.334G>A (p.Val112Ile) c.418G>A (p.Val140Ile) c.2407G>A (p.Val803Ile) c.691G>A (p.Val231Ile) | ClinVar dbSNP |
| 2 | g.29220814A>C | CA346473152 | ALK | c.3537T>G (p.Ile1179Met) c.764T>G n.414T>G c.333T>G (p.Ile111Met) c.417T>G (p.Ile139Met) c.2406T>G (p.Ile802Met) c.690T>G (p.Ile230Met) | |
| 2 | g.29220814A>G | CA425619441 | ALK | c.3537T>C (p.Ile1179=) c.764T>C n.414T>C c.333T>C (p.Ile111=) c.417T>C (p.Ile139=) c.2406T>C (p.Ile802=) c.690T>C (p.Ile230=) | ClinVar dbSNP |
| 2 | g.29220814A>T | CA425619442 | ALK | c.3537T>A (p.Ile1179=) c.764T>A n.414T>A c.333T>A (p.Ile111=) c.417T>A (p.Ile139=) c.2406T>A (p.Ile802=) c.690T>A (p.Ile230=) | dbSNP |
| 2 | g.29220815dup | CA2573134529 | ALK | c.3537dup (p.Val1180CysfsTer?) c.764dup n.414dup c.333dup (p.Val112CysfsTer?) c.417dup (p.Val140CysfsTer?) c.2406dup (p.Val803CysfsTer?) c.690dup (p.Val231CysfsTer?) | ClinVar dbSNP |
| 2 | g.29220815A>C | CA346473153 | ALK | c.3536T>G (p.Ile1179Ser) c.763T>G n.413T>G c.332T>G (p.Ile111Ser) c.416T>G (p.Ile139Ser) c.2405T>G (p.Ile802Ser) c.689T>G (p.Ile230Ser) | dbSNP |
| 2 | g.29220815A>G | CA346473154 | ALK | c.3536T>C (p.Ile1179Thr) c.763T>C n.413T>C c.332T>C (p.Ile111Thr) c.416T>C (p.Ile139Thr) c.2405T>C (p.Ile802Thr) c.689T>C (p.Ile230Thr) | ClinVar dbSNP gnomAD v4 |
| 2 | g.29220815A>T | CA346473155 | ALK | c.3536T>A (p.Ile1179Asn) c.763T>A n.413T>A c.332T>A (p.Ile111Asn) c.416T>A (p.Ile139Asn) c.2405T>A (p.Ile802Asn) c.689T>A (p.Ile230Asn) | dbSNP |
| 2 | g.29220816T>A | CA346473156 | ALK | c.3535A>T (p.Ile1179Phe) c.762A>T n.412A>T c.331A>T (p.Ile111Phe) c.415A>T (p.Ile139Phe) c.2404A>T (p.Ile802Phe) c.688A>T (p.Ile230Phe) | dbSNP |
| 2 | g.29220816T>C | CA346473157 | ALK | c.3535A>G (p.Ile1179Val) c.762A>G n.412A>G c.331A>G (p.Ile111Val) c.415A>G (p.Ile139Val) c.2404A>G (p.Ile802Val) c.688A>G (p.Ile230Val) | dbSNP gnomAD v2 gnomAD v4 |
| 2 | g.29220816T>G | CA346473158 | ALK | c.3535A>C (p.Ile1179Leu) c.762A>C n.412A>C c.331A>C (p.Ile111Leu) c.415A>C (p.Ile139Leu) c.2404A>C (p.Ile802Leu) c.688A>C (p.Ile230Leu) | |
| 2 | g.29220816T= | CA1241089800 | ALK | c.3535A= (p.Ile1179=) c.762A= n.412A= c.331A= (p.Ile111=) c.415A= (p.Ile139=) c.2404A= (p.Ile802=) c.688A= (p.Ile230=) | |
| 2 | g.29220817G>A | CA425619443 | ALK | c.3534C>T (p.Asn1178=) c.761C>T n.411C>T c.330C>T (p.Asn110=) c.414C>T (p.Asn138=) c.2403C>T (p.Asn801=) c.687C>T (p.Asn229=) | ClinVar dbSNP |
| 2 | g.29220817G>C | CA346473159 | ALK | c.3534C>G (p.Asn1178Lys) c.761C>G n.411C>G c.330C>G (p.Asn110Lys) c.414C>G (p.Asn138Lys) c.2403C>G (p.Asn801Lys) c.687C>G (p.Asn229Lys) | dbSNP |
| 2 | g.29220817G= | CA1241089801 | ALK | c.3534C= (p.Asn1178=) c.761C= n.411C= c.330C= (p.Asn110=) c.414C= (p.Asn138=) c.2403C= (p.Asn801=) c.687C= (p.Asn229=) | |
| 2 | g.29220817G>T | CA346473160 | ALK | c.3534C>A (p.Asn1178Lys) c.761C>A n.411C>A c.330C>A (p.Asn110Lys) c.414C>A (p.Asn138Lys) c.2403C>A (p.Asn801Lys) c.687C>A (p.Asn229Lys) | dbSNP |
| 2 | g.29220818T>A | CA346473163 | ALK | c.3533A>T (p.Asn1178Ile) c.760A>T n.410A>T c.329A>T (p.Asn110Ile) c.413A>T (p.Asn138Ile) c.2402A>T (p.Asn801Ile) c.686A>T (p.Asn229Ile) | dbSNP |
| 2 | g.29220818T>C | CA346473162 | ALK | c.3533A>G (p.Asn1178Ser) c.760A>G n.410A>G c.329A>G (p.Asn110Ser) c.413A>G (p.Asn138Ser) c.2402A>G (p.Asn801Ser) c.686A>G (p.Asn229Ser) | dbSNP |
| 2 | g.29220818T>G | CA346473161 | ALK | c.3533A>C (p.Asn1178Thr) c.760A>C n.410A>C c.329A>C (p.Asn110Thr) c.413A>C (p.Asn138Thr) c.2402A>C (p.Asn801Thr) c.686A>C (p.Asn229Thr) | dbSNP |
| 2 | g.29220820_29220834del | CA2576925231 | ALK | c.3519_3533del (p.Lys1173_Gln1177del) c.746_760del n.396_410del c.315_329del (p.Lys105_Gln109del) c.399_413del (p.Lys133_Gln137del) c.2388_2402del (p.Lys796_Gln800del) c.672_686del (p.Lys224_Gln228del) | |
| 2 | g.29220819T>A | CA346473164 | ALK | c.3532A>T (p.Asn1178Tyr) c.759A>T n.409A>T c.328A>T (p.Asn110Tyr) c.412A>T (p.Asn138Tyr) c.2401A>T (p.Asn801Tyr) c.685A>T (p.Asn229Tyr) | dbSNP |
| 2 | g.29220819T>C | CA346473165 | ALK | c.3532A>G (p.Asn1178Asp) c.759A>G n.409A>G c.328A>G (p.Asn110Asp) c.412A>G (p.Asn138Asp) c.2401A>G (p.Asn801Asp) c.685A>G (p.Asn229Asp) | |
| 2 | g.29220819T>G | CA346473166 | ALK | c.3532A>C (p.Asn1178His) c.759A>C n.409A>C c.328A>C (p.Asn110His) c.412A>C (p.Asn138His) c.2401A>C (p.Asn801His) c.685A>C (p.Asn229His) | |
| 2 | g.29220820C>A | CA346473167 | ALK | c.3531G>T (p.Gln1177His) c.758G>T n.408G>T c.327G>T (p.Gln109His) c.411G>T (p.Gln137His) c.2400G>T (p.Gln800His) c.684G>T (p.Gln228His) | dbSNP |
| 2 | g.29220820C>G | CA346473168 | ALK | c.3531G>C (p.Gln1177His) c.758G>C n.408G>C c.327G>C (p.Gln109His) c.411G>C (p.Gln137His) c.2400G>C (p.Gln800His) c.684G>C (p.Gln228His) | dbSNP |
| 2 | g.29220820C>T | CA425619444 | ALK | c.3531G>A (p.Gln1177=) c.758G>A n.408G>A c.327G>A (p.Gln109=) c.411G>A (p.Gln137=) c.2400G>A (p.Gln800=) c.684G>A (p.Gln228=) | dbSNP |
| 2 | g.29220821T>A | CA346473169 | ALK | c.3530A>T (p.Gln1177Leu) c.757A>T n.407A>T c.326A>T (p.Gln109Leu) c.410A>T (p.Gln137Leu) c.2399A>T (p.Gln800Leu) c.683A>T (p.Gln228Leu) | |
| 2 | g.29220821T>C | CA346473170 | ALK | c.3530A>G (p.Gln1177Arg) c.757A>G n.407A>G c.326A>G (p.Gln109Arg) c.410A>G (p.Gln137Arg) c.2399A>G (p.Gln800Arg) c.683A>G (p.Gln228Arg) | |
| 2 | g.29220821T>G | CA16610895 | ALK | c.3530A>C (p.Gln1177Pro) c.757A>C n.407A>C c.326A>C (p.Gln109Pro) c.410A>C (p.Gln137Pro) c.2399A>C (p.Gln800Pro) c.683A>C (p.Gln228Pro) | ClinVar dbSNP |
| 2 | g.29220821T= | CA1241089802 | ALK | c.3530A= (p.Gln1177=) c.757A= n.407A= c.326A= (p.Gln109=) c.410A= (p.Gln137=) c.2399A= (p.Gln800=) c.683A= (p.Gln228=) | |
| 2 | g.29220822G>A | CA346473171 | ALK | c.3529C>T (p.Gln1177Ter) c.756C>T n.406C>T c.325C>T (p.Gln109Ter) c.409C>T (p.Gln137Ter) c.2398C>T (p.Gln800Ter) c.682C>T (p.Gln228Ter) | dbSNP |
| 2 | g.29220822G>C | CA346473172 | ALK | c.3529C>G (p.Gln1177Glu) c.756C>G n.406C>G c.325C>G (p.Gln109Glu) c.409C>G (p.Gln137Glu) c.2398C>G (p.Gln800Glu) c.682C>G (p.Gln228Glu) | ClinVar dbSNP |
| 2 | g.29220822G>T | CA346473173 | ALK | c.3529C>A (p.Gln1177Lys) c.756C>A n.406C>A c.325C>A (p.Gln109Lys) c.409C>A (p.Gln137Lys) c.2398C>A (p.Gln800Lys) c.682C>A (p.Gln228Lys) | |
| 2 | g.29220823G>A | CA425619445 | ALK | c.3528C>T (p.His1176=) c.755C>T n.405C>T c.324C>T (p.His108=) c.408C>T (p.His136=) c.2397C>T (p.His799=) c.681C>T (p.His227=) | ClinVar dbSNP gnomAD v4 |
| 2 | g.29220823G>C | CA346473174 | ALK | c.3528C>G (p.His1176Gln) c.755C>G n.405C>G c.324C>G (p.His108Gln) c.408C>G (p.His136Gln) c.2397C>G (p.His799Gln) c.681C>G (p.His227Gln) | dbSNP |
| 2 | g.29220823G>T | CA346473175 | ALK | c.3528C>A (p.His1176Gln) c.755C>A n.405C>A c.324C>A (p.His108Gln) c.408C>A (p.His136Gln) c.2397C>A (p.His799Gln) c.681C>A (p.His227Gln) | dbSNP |
| 2 | g.29220824T>A | CA346473178 | ALK | c.3527A>T (p.His1176Leu) c.754A>T n.404A>T c.323A>T (p.His108Leu) c.407A>T (p.His136Leu) c.2396A>T (p.His799Leu) c.680A>T (p.His227Leu) | |
| 2 | g.29220824T>C | CA346473176 | ALK | c.3527A>G (p.His1176Arg) c.754A>G n.404A>G c.323A>G (p.His108Arg) c.407A>G (p.His136Arg) c.2396A>G (p.His799Arg) c.680A>G (p.His227Arg) | |
| 2 | g.29220824T>G | CA346473177 | ALK | c.3527A>C (p.His1176Pro) c.754A>C n.404A>C c.323A>C (p.His108Pro) c.407A>C (p.His136Pro) c.2396A>C (p.His799Pro) c.680A>C (p.His227Pro) | |
| 2 | g.29220825G>A | CA346473179 | ALK | c.3526C>T (p.His1176Tyr) c.753C>T n.403C>T c.322C>T (p.His108Tyr) c.406C>T (p.His136Tyr) c.2395C>T (p.His799Tyr) c.679C>T (p.His227Tyr) | dbSNP |
| 2 | g.29220825G>C | CA346473180 | ALK | c.3526C>G (p.His1176Asp) c.753C>G n.403C>G c.322C>G (p.His108Asp) c.406C>G (p.His136Asp) c.2395C>G (p.His799Asp) c.679C>G (p.His227Asp) | dbSNP |
| 2 | g.29220825G= | CA1241089803 | ALK | c.3526C= (p.His1176=) c.753C= n.403C= c.322C= (p.His108=) c.406C= (p.His136=) c.2395C= (p.His799=) c.679C= (p.His227=) | |
| 2 | g.29220825G>T | CA346473181 | ALK | c.3526C>A (p.His1176Asn) c.753C>A n.403C>A c.322C>A (p.His108Asn) c.406C>A (p.His136Asn) c.2395C>A (p.His799Asn) c.679C>A (p.His227Asn) | ClinVar dbSNP |
| 2 | g.29220826G>A | CA425619446 | ALK | c.3525C>T (p.Asn1175=) c.752C>T n.402C>T c.321C>T (p.Asn107=) c.405C>T (p.Asn135=) c.2394C>T (p.Asn798=) c.678C>T (p.Asn226=) | dbSNP |
| 2 | g.29220826G>C | CA346473182 | ALK | c.3525C>G (p.Asn1175Lys) c.752C>G n.402C>G c.321C>G (p.Asn107Lys) c.405C>G (p.Asn135Lys) c.2394C>G (p.Asn798Lys) c.678C>G (p.Asn226Lys) | dbSNP |
| 2 | g.29220826G>T | CA346473183 | ALK | c.3525C>A (p.Asn1175Lys) c.752C>A n.402C>A c.321C>A (p.Asn107Lys) c.405C>A (p.Asn135Lys) c.2394C>A (p.Asn798Lys) c.678C>A (p.Asn226Lys) | dbSNP |
| 2 | g.29220827T>A | CA346473184 | ALK | c.3524A>T (p.Asn1175Ile) c.751A>T n.401A>T c.320A>T (p.Asn107Ile) c.404A>T (p.Asn135Ile) c.2393A>T (p.Asn798Ile) c.677A>T (p.Asn226Ile) | dbSNP |
| 2 | g.29220827T>C | CA1593867 | ALK | c.3524A>G (p.Asn1175Ser) c.751A>G n.401A>G c.320A>G (p.Asn107Ser) c.404A>G (p.Asn135Ser) c.2393A>G (p.Asn798Ser) c.677A>G (p.Asn226Ser) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 2 | g.29220827T>G | CA346473185 | ALK | c.3524A>C (p.Asn1175Thr) c.751A>C n.401A>C c.320A>C (p.Asn107Thr) c.404A>C (p.Asn135Thr) c.2393A>C (p.Asn798Thr) c.677A>C (p.Asn226Thr) | dbSNP |
| 2 | g.29220827T= | CA1241089804 | ALK | c.3524A= (p.Asn1175=) c.751A= n.401A= c.320A= (p.Asn107=) c.404A= (p.Asn135=) c.2393A= (p.Asn798=) c.677A= (p.Asn226=) | |
| 2 | g.29220828T>A | CA346473186 | ALK | c.3523A>T (p.Asn1175Tyr) c.750A>T n.400A>T c.319A>T (p.Asn107Tyr) c.403A>T (p.Asn135Tyr) c.2392A>T (p.Asn798Tyr) c.676A>T (p.Asn226Tyr) | dbSNP |
| 2 | g.29220828T>C | CA346473187 | ALK | c.3523A>G (p.Asn1175Asp) c.750A>G n.400A>G c.319A>G (p.Asn107Asp) c.403A>G (p.Asn135Asp) c.2392A>G (p.Asn798Asp) c.676A>G (p.Asn226Asp) | dbSNP |
| 2 | g.29220828T>G | CA346473188 | ALK | c.3523A>C (p.Asn1175His) c.750A>C n.400A>C c.319A>C (p.Asn107His) c.403A>C (p.Asn135His) c.2392A>C (p.Asn798His) c.676A>C (p.Asn226His) | |
| 2 | g.29220829G>A | CA425619447 | ALK | c.3522C>T (p.Phe1174=) c.749C>T n.399C>T c.318C>T (p.Phe106=) c.402C>T (p.Phe134=) c.2391C>T (p.Phe797=) c.675C>T (p.Phe225=) | ClinVar dbSNP |
| 2 | g.29220829G>C | CA279616 | ALK | c.3522C>G (p.Phe1174Leu) c.749C>G n.399C>G c.318C>G (p.Phe106Leu) c.402C>G (p.Phe134Leu) c.2391C>G (p.Phe797Leu) c.675C>G (p.Phe225Leu) | ClinVar dbSNP COSMIC |
| 2 | g.29220829G= | CA1241089805 | ALK | c.3522C= (p.Phe1174=) c.749C= n.399C= c.318C= (p.Phe106=) c.402C= (p.Phe134=) c.2391C= (p.Phe797=) c.675C= (p.Phe225=) | |
| 2 | g.29220829G>T | CA279586 | ALK | c.3522C>A (p.Phe1174Leu) c.749C>A n.399C>A c.318C>A (p.Phe106Leu) c.402C>A (p.Phe134Leu) c.2391C>A (p.Phe797Leu) c.675C>A (p.Phe225Leu) | ClinVar dbSNP COSMIC |
| 2 | g.29220830A= | CA1241089806 | ALK | c.3521T= (p.Phe1174=) c.748T= n.398T= c.317T= (p.Phe106=) c.401T= (p.Phe134=) c.2390T= (p.Phe797=) c.674T= (p.Phe225=) | |
| 2 | g.29220830A>C | CA16602370 | ALK | c.3521T>G (p.Phe1174Cys) c.748T>G n.398T>G c.317T>G (p.Phe106Cys) c.401T>G (p.Phe134Cys) c.2390T>G (p.Phe797Cys) c.674T>G (p.Phe225Cys) | ClinVar dbSNP COSMIC |
| 2 | g.29220830A>G | CA346473190 | ALK | c.3521T>C (p.Phe1174Ser) c.748T>C n.398T>C c.317T>C (p.Phe106Ser) c.401T>C (p.Phe134Ser) c.2390T>C (p.Phe797Ser) c.674T>C (p.Phe225Ser) | dbSNP COSMIC |
| 2 | g.29220830A>T | CA346473189 | ALK | c.3521T>A (p.Phe1174Tyr) c.748T>A n.398T>A c.317T>A (p.Phe106Tyr) c.401T>A (p.Phe134Tyr) c.2390T>A (p.Phe797Tyr) c.674T>A (p.Phe225Tyr) | dbSNP |
| 2 | g.29220831A= | CA1241089807 | ALK | c.3520T= (p.Phe1174=) c.747T= n.397T= c.316T= (p.Phe106=) c.400T= (p.Phe134=) c.2389T= (p.Phe797=) c.673T= (p.Phe225=) | |
| 2 | g.29220831A>C | CA345001 | ALK | c.3520T>G (p.Phe1174Val) c.747T>G n.397T>G c.316T>G (p.Phe106Val) c.400T>G (p.Phe134Val) c.2389T>G (p.Phe797Val) c.673T>G (p.Phe225Val) | ClinVar dbSNP COSMIC |
| 2 | g.29220831A>G | CA277829 | ALK | c.3520T>C (p.Phe1174Leu) c.747T>C n.397T>C c.316T>C (p.Phe106Leu) c.400T>C (p.Phe134Leu) c.2389T>C (p.Phe797Leu) c.673T>C (p.Phe225Leu) | ClinVar dbSNP COSMIC |
| 2 | g.29220831A>T | CA277834 | ALK | c.3520T>A (p.Phe1174Ile) c.747T>A n.397T>A c.316T>A (p.Phe106Ile) c.400T>A (p.Phe134Ile) c.2389T>A (p.Phe797Ile) c.673T>A (p.Phe225Ile) | ClinVar dbSNP COSMIC |
| 2 | g.29220832T>A | CA346473191 | ALK | c.3519A>T (p.Lys1173Asn) c.746A>T n.396A>T c.315A>T (p.Lys105Asn) c.399A>T (p.Lys133Asn) c.2388A>T (p.Lys796Asn) c.672A>T (p.Lys224Asn) | dbSNP |
| 2 | g.29220832T>C | CA425619448 | ALK | c.3519A>G (p.Lys1173=) c.746A>G n.396A>G c.315A>G (p.Lys105=) c.399A>G (p.Lys133=) c.2388A>G (p.Lys796=) c.672A>G (p.Lys224=) | dbSNP COSMIC |
| 2 | g.29220832T>G | CA346473192 | ALK | c.3519A>C (p.Lys1173Asn) c.746A>C n.396A>C c.315A>C (p.Lys105Asn) c.399A>C (p.Lys133Asn) c.2388A>C (p.Lys796Asn) c.672A>C (p.Lys224Asn) | dbSNP |
| 2 | g.29220833T>A | CA346473193 | ALK | c.3518A>T (p.Lys1173Ile) c.745A>T n.395A>T c.314A>T (p.Lys105Ile) c.398A>T (p.Lys133Ile) c.2387A>T (p.Lys796Ile) c.671A>T (p.Lys224Ile) | |
| 2 | g.29220833T>C | CA346473195 | ALK | c.3518A>G (p.Lys1173Arg) c.745A>G n.395A>G c.314A>G (p.Lys105Arg) c.398A>G (p.Lys133Arg) c.2387A>G (p.Lys796Arg) c.671A>G (p.Lys224Arg) | |
| 2 | g.29220833T>G | CA346473194 | ALK | c.3518A>C (p.Lys1173Thr) c.745A>C n.395A>C c.314A>C (p.Lys105Thr) c.398A>C (p.Lys133Thr) c.2387A>C (p.Lys796Thr) c.671A>C (p.Lys224Thr) | dbSNP |
| 2 | g.29220834T>A | CA346473196 | ALK | c.3517A>T (p.Lys1173Ter) c.744A>T n.394A>T c.313A>T (p.Lys105Ter) c.397A>T (p.Lys133Ter) c.2386A>T (p.Lys796Ter) c.670A>T (p.Lys224Ter) | dbSNP |
| 2 | g.29220834T>C | CA346473197 | ALK | c.3517A>G (p.Lys1173Glu) c.744A>G n.394A>G c.313A>G (p.Lys105Glu) c.397A>G (p.Lys133Glu) c.2386A>G (p.Lys796Glu) c.670A>G (p.Lys224Glu) | |
| 2 | g.29220834T>G | CA346473198 | ALK | c.3517A>C (p.Lys1173Gln) c.744A>C n.394A>C c.313A>C (p.Lys105Gln) c.397A>C (p.Lys133Gln) c.2386A>C (p.Lys796Gln) c.670A>C (p.Lys224Gln) | |
| 2 | g.29220835G>A | CA425619449 | ALK | c.3516C>T (p.Ser1172=) c.743C>T n.393C>T c.312C>T (p.Ser104=) c.396C>T (p.Ser132=) c.2385C>T (p.Ser795=) c.669C>T (p.Ser223=) | dbSNP |
| 2 | g.29220835G>C | CA346473199 | ALK | c.3516C>G (p.Ser1172Arg) c.743C>G n.393C>G c.312C>G (p.Ser104Arg) c.396C>G (p.Ser132Arg) c.2385C>G (p.Ser795Arg) c.669C>G (p.Ser223Arg) | ClinVar dbSNP gnomAD v4 |
| 2 | g.29220835G>T | CA346473200 | ALK | c.3516C>A (p.Ser1172Arg) c.743C>A n.393C>A c.312C>A (p.Ser104Arg) c.396C>A (p.Ser132Arg) c.2385C>A (p.Ser795Arg) c.669C>A (p.Ser223Arg) |