UPDATE - Protein Allele ID & Protein Sequence HGVS Requests Partially Restored
Protein allele requests are no longer disabled.
Currently, hypothetical explanatory transcript generation is not part of the response and is being investigated.
Protein allele requests are no longer disabled.
Currently, hypothetical explanatory transcript generation is not part of the response and is being investigated.
| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 2 | g.29222490C>A | CA2698771831 | ALK | c.3450+27G>T (n.3450+27G>T) c.677+27G>T n.327+27G>T c.246+27G>T (n.246+27G>T) c.330+27G>T (n.330+27G>T) c.144+27G>T (n.144+27G>T) c.2319+27G>T (n.2319+27G>T) c.603+27G>T (n.603+27G>T) | dbSNP |
| 2 | g.29222490C= | CA1241090585 | ALK | c.3450+27G= (n.3450+27G=) c.677+27G= n.327+27G= c.246+27G= (n.246+27G=) c.330+27G= (n.330+27G=) c.144+27G= (n.144+27G=) c.2319+27G= (n.2319+27G=) c.603+27G= (n.603+27G=) | |
| 2 | g.29222490C>G | CA1593950 | ALK | c.3450+27G>C (n.3450+27G>C) c.677+27G>C n.327+27G>C c.246+27G>C (n.246+27G>C) c.330+27G>C (n.330+27G>C) c.144+27G>C (n.144+27G>C) c.2319+27G>C (n.2319+27G>C) c.603+27G>C (n.603+27G>C) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 2 | g.29222490C>T | CA2658458447 | ALK | c.3450+27G>A (n.3450+27G>A) c.677+27G>A n.327+27G>A c.246+27G>A (n.246+27G>A) c.330+27G>A (n.330+27G>A) c.144+27G>A (n.144+27G>A) c.2319+27G>A (n.2319+27G>A) c.603+27G>A (n.603+27G>A) | dbSNP gnomAD v4 |
| 2 | g.29222491A>G | CA2698975247 | ALK | c.3450+26T>C (n.3450+26T>C) c.677+26T>C n.327+26T>C c.246+26T>C (n.246+26T>C) c.330+26T>C (n.330+26T>C) c.144+26T>C (n.144+26T>C) c.2319+26T>C (n.2319+26T>C) c.603+26T>C (n.603+26T>C) | dbSNP |
| 2 | g.29222491A>T | CA2698975222 | ALK | c.3450+26T>A (n.3450+26T>A) c.677+26T>A n.327+26T>A c.246+26T>A (n.246+26T>A) c.330+26T>A (n.330+26T>A) c.144+26T>A (n.144+26T>A) c.2319+26T>A (n.2319+26T>A) c.603+26T>A (n.603+26T>A) | dbSNP |
| 2 | g.29222491_29222492delinsAG | CA1241090586 | ALK | c.3450+25_3450+26delinsCT (n.3450+25_3450+26delinsCT) c.677+25_677+26delinsCT n.327+25_327+26delinsCT c.246+25_246+26delinsCT (n.246+25_246+26delinsCT) c.330+25_330+26delinsCT (n.330+25_330+26delinsCT) c.144+25_144+26delinsCT (n.144+25_144+26delinsCT) c.2319+25_2319+26delinsCT (n.2319+25_2319+26delinsCT) c.603+25_603+26delinsCT (n.603+25_603+26delinsCT) | |
| 2 | g.29222492G>A | CA1241090587 | ALK | c.3450+25C>T (n.3450+25C>T) c.677+25C>T n.327+25C>T c.246+25C>T (n.246+25C>T) c.330+25C>T (n.330+25C>T) c.144+25C>T (n.144+25C>T) c.2319+25C>T (n.2319+25C>T) c.603+25C>T (n.603+25C>T) | dbSNP |
| 2 | g.29222492G>C | CA1593951 | ALK | c.3450+25C>G (n.3450+25C>G) c.677+25C>G n.327+25C>G c.246+25C>G (n.246+25C>G) c.330+25C>G (n.330+25C>G) c.144+25C>G (n.144+25C>G) c.2319+25C>G (n.2319+25C>G) c.603+25C>G (n.603+25C>G) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 2 | g.29222492G= | CA1241090588 | ALK | c.3450+25C= (n.3450+25C=) c.677+25C= n.327+25C= c.246+25C= (n.246+25C=) c.330+25C= (n.330+25C=) c.144+25C= (n.144+25C=) c.2319+25C= (n.2319+25C=) c.603+25C= (n.603+25C=) | |
| 2 | g.29222492G>T | CA2698773080 | ALK | c.3450+25C>A (n.3450+25C>A) c.677+25C>A n.327+25C>A c.246+25C>A (n.246+25C>A) c.330+25C>A (n.330+25C>A) c.144+25C>A (n.144+25C>A) c.2319+25C>A (n.2319+25C>A) c.603+25C>A (n.603+25C>A) | dbSNP |
| 2 | g.29222493del | CA1028815019 | ALK | c.3450+25del (n.3450+25del) c.677+25del n.327+25del c.246+25del (n.246+25del) c.330+25del (n.330+25del) c.144+25del (n.144+25del) c.2319+25del (n.2319+25del) c.603+25del (n.603+25del) | dbSNP gnomAD v3 gnomAD v4 |
| 2 | g.29222493G>A | CA2698975324 | ALK | c.3450+24C>T (n.3450+24C>T) c.677+24C>T n.327+24C>T c.246+24C>T (n.246+24C>T) c.330+24C>T (n.330+24C>T) c.144+24C>T (n.144+24C>T) c.2319+24C>T (n.2319+24C>T) c.603+24C>T (n.603+24C>T) | dbSNP |
| 2 | g.29222493G>C | CA2698975318 | ALK | c.3450+24C>G (n.3450+24C>G) c.677+24C>G n.327+24C>G c.246+24C>G (n.246+24C>G) c.330+24C>G (n.330+24C>G) c.144+24C>G (n.144+24C>G) c.2319+24C>G (n.2319+24C>G) c.603+24C>G (n.603+24C>G) | dbSNP |
| 2 | g.29222493G>T | CA2698975321 | ALK | c.3450+24C>A (n.3450+24C>A) c.677+24C>A n.327+24C>A c.246+24C>A (n.246+24C>A) c.330+24C>A (n.330+24C>A) c.144+24C>A (n.144+24C>A) c.2319+24C>A (n.2319+24C>A) c.603+24C>A (n.603+24C>A) | dbSNP |
| 2 | g.29222494C>A | CA2698975341 | ALK | c.3450+23G>T (n.3450+23G>T) c.677+23G>T n.327+23G>T c.246+23G>T (n.246+23G>T) c.330+23G>T (n.330+23G>T) c.144+23G>T (n.144+23G>T) c.2319+23G>T (n.2319+23G>T) c.603+23G>T (n.603+23G>T) | dbSNP |
| 2 | g.29222494C>G | CA2698975345 | ALK | c.3450+23G>C (n.3450+23G>C) c.677+23G>C n.327+23G>C c.246+23G>C (n.246+23G>C) c.330+23G>C (n.330+23G>C) c.144+23G>C (n.144+23G>C) c.2319+23G>C (n.2319+23G>C) c.603+23G>C (n.603+23G>C) | dbSNP |
| 2 | g.29222495T>A | CA2698785791 | ALK | c.3450+22A>T (n.3450+22A>T) c.677+22A>T n.327+22A>T c.246+22A>T (n.246+22A>T) c.330+22A>T (n.330+22A>T) c.144+22A>T (n.144+22A>T) c.2319+22A>T (n.2319+22A>T) c.603+22A>T (n.603+22A>T) | dbSNP |
| 2 | g.29222495T>C | CA2698785790 | ALK | c.3450+22A>G (n.3450+22A>G) c.677+22A>G n.327+22A>G c.246+22A>G (n.246+22A>G) c.330+22A>G (n.330+22A>G) c.144+22A>G (n.144+22A>G) c.2319+22A>G (n.2319+22A>G) c.603+22A>G (n.603+22A>G) | dbSNP |
| 2 | g.29222495T>G | CA44631315 | ALK | c.3450+22A>C (n.3450+22A>C) c.677+22A>C n.327+22A>C c.246+22A>C (n.246+22A>C) c.330+22A>C (n.330+22A>C) c.144+22A>C (n.144+22A>C) c.2319+22A>C (n.2319+22A>C) c.603+22A>C (n.603+22A>C) | dbSNP |
| 2 | g.29222495T= | CA1241090589 | ALK | c.3450+22A= (n.3450+22A=) c.677+22A= n.327+22A= c.246+22A= (n.246+22A=) c.330+22A= (n.330+22A=) c.144+22A= (n.144+22A=) c.2319+22A= (n.2319+22A=) c.603+22A= (n.603+22A=) | |
| 2 | g.29222496C>A | CA2698790337 | ALK | c.3450+21G>T (n.3450+21G>T) c.677+21G>T n.327+21G>T c.246+21G>T (n.246+21G>T) c.330+21G>T (n.330+21G>T) c.144+21G>T (n.144+21G>T) c.2319+21G>T (n.2319+21G>T) c.603+21G>T (n.603+21G>T) | dbSNP |
| 2 | g.29222496C= | CA1241090591 | ALK | c.3450+21G= (n.3450+21G=) c.677+21G= n.327+21G= c.246+21G= (n.246+21G=) c.330+21G= (n.330+21G=) c.144+21G= (n.144+21G=) c.2319+21G= (n.2319+21G=) c.603+21G= (n.603+21G=) | |
| 2 | g.29222496C>G | CA2658458454 | ALK | c.3450+21G>C (n.3450+21G>C) c.677+21G>C n.327+21G>C c.246+21G>C (n.246+21G>C) c.330+21G>C (n.330+21G>C) c.144+21G>C (n.144+21G>C) c.2319+21G>C (n.2319+21G>C) c.603+21G>C (n.603+21G>C) | dbSNP gnomAD v4 |
| 2 | g.29222496C>T | CA531766922 | ALK | c.3450+21G>A (n.3450+21G>A) c.677+21G>A n.327+21G>A c.246+21G>A (n.246+21G>A) c.330+21G>A (n.330+21G>A) c.144+21G>A (n.144+21G>A) c.2319+21G>A (n.2319+21G>A) c.603+21G>A (n.603+21G>A) | dbSNP gnomAD v2 gnomAD v4 |
| 2 | g.29222496_29222498delinsCAA | CA1241090590 | ALK | c.3450+19_3450+21delinsTTG (n.3450+19_3450+21delinsTTG) c.677+19_677+21delinsTTG n.327+19_327+21delinsTTG c.246+19_246+21delinsTTG (n.246+19_246+21delinsTTG) c.330+19_330+21delinsTTG (n.330+19_330+21delinsTTG) c.144+19_144+21delinsTTG (n.144+19_144+21delinsTTG) c.2319+19_2319+21delinsTTG (n.2319+19_2319+21delinsTTG) c.603+19_603+21delinsTTG (n.603+19_603+21delinsTTG) | |
| 2 | g.29222497A>C | CA2658458455 | ALK | c.3450+20T>G (n.3450+20T>G) c.677+20T>G n.327+20T>G c.246+20T>G (n.246+20T>G) c.330+20T>G (n.330+20T>G) c.144+20T>G (n.144+20T>G) c.2319+20T>G (n.2319+20T>G) c.603+20T>G (n.603+20T>G) | gnomAD v4 |
| 2 | g.29222497A>G | CA2698975364 | ALK | c.3450+20T>C (n.3450+20T>C) c.677+20T>C n.327+20T>C c.246+20T>C (n.246+20T>C) c.330+20T>C (n.330+20T>C) c.144+20T>C (n.144+20T>C) c.2319+20T>C (n.2319+20T>C) c.603+20T>C (n.603+20T>C) | dbSNP |
| 2 | g.29222497_29222498del | CA1593952 | ALK | c.3450+19_3450+20del (n.3450+19_3450+20del) c.677+19_677+20del n.327+19_327+20del c.246+19_246+20del (n.246+19_246+20del) c.330+19_330+20del (n.330+19_330+20del) c.144+19_144+20del (n.144+19_144+20del) c.2319+19_2319+20del (n.2319+19_2319+20del) c.603+19_603+20del (n.603+19_603+20del) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 2 | g.29222498A>C | CA2698975411 | ALK | c.3450+19T>G (n.3450+19T>G) c.677+19T>G n.327+19T>G c.246+19T>G (n.246+19T>G) c.330+19T>G (n.330+19T>G) c.144+19T>G (n.144+19T>G) c.2319+19T>G (n.2319+19T>G) c.603+19T>G (n.603+19T>G) | dbSNP |
| 2 | g.29222498A>G | CA2526966341 | ALK | c.3450+19T>C (n.3450+19T>C) c.677+19T>C n.327+19T>C c.246+19T>C (n.246+19T>C) c.330+19T>C (n.330+19T>C) c.144+19T>C (n.144+19T>C) c.2319+19T>C (n.2319+19T>C) c.603+19T>C (n.603+19T>C) | dbSNP |
| 2 | g.29222498A>T | CA2698975438 | ALK | c.3450+19T>A (n.3450+19T>A) c.677+19T>A n.327+19T>A c.246+19T>A (n.246+19T>A) c.330+19T>A (n.330+19T>A) c.144+19T>A (n.144+19T>A) c.2319+19T>A (n.2319+19T>A) c.603+19T>A (n.603+19T>A) | dbSNP |
| 2 | g.29222499G>A | CA2698975441 | ALK | c.3450+18C>T (n.3450+18C>T) c.677+18C>T n.327+18C>T c.246+18C>T (n.246+18C>T) c.330+18C>T (n.330+18C>T) c.144+18C>T (n.144+18C>T) c.2319+18C>T (n.2319+18C>T) c.603+18C>T (n.603+18C>T) | dbSNP |
| 2 | g.29222499G>C | CA2698975443 | ALK | c.3450+18C>G (n.3450+18C>G) c.677+18C>G n.327+18C>G c.246+18C>G (n.246+18C>G) c.330+18C>G (n.330+18C>G) c.144+18C>G (n.144+18C>G) c.2319+18C>G (n.2319+18C>G) c.603+18C>G (n.603+18C>G) | dbSNP |
| 2 | g.29222499G>T | CA2698975445 | ALK | c.3450+18C>A (n.3450+18C>A) c.677+18C>A n.327+18C>A c.246+18C>A (n.246+18C>A) c.330+18C>A (n.330+18C>A) c.144+18C>A (n.144+18C>A) c.2319+18C>A (n.2319+18C>A) c.603+18C>A (n.603+18C>A) | dbSNP |
| 2 | g.29222500A>G | CA2698975447 | ALK | c.3450+17T>C (n.3450+17T>C) c.677+17T>C n.327+17T>C c.246+17T>C (n.246+17T>C) c.330+17T>C (n.330+17T>C) c.144+17T>C (n.144+17T>C) c.2319+17T>C (n.2319+17T>C) c.603+17T>C (n.603+17T>C) | dbSNP |
| 2 | g.29222500A>T | CA2698975455 | ALK | c.3450+17T>A (n.3450+17T>A) c.677+17T>A n.327+17T>A c.246+17T>A (n.246+17T>A) c.330+17T>A (n.330+17T>A) c.144+17T>A (n.144+17T>A) c.2319+17T>A (n.2319+17T>A) c.603+17T>A (n.603+17T>A) | dbSNP |
| 2 | g.29222501G>A | CA1241090593 | ALK | c.3450+16C>T (n.3450+16C>T) c.677+16C>T n.327+16C>T c.246+16C>T (n.246+16C>T) c.330+16C>T (n.330+16C>T) c.144+16C>T (n.144+16C>T) c.2319+16C>T (n.2319+16C>T) c.603+16C>T (n.603+16C>T) | ClinVar dbSNP |
| 2 | g.29222501G>C | CA2698823725 | ALK | c.3450+16C>G (n.3450+16C>G) c.677+16C>G n.327+16C>G c.246+16C>G (n.246+16C>G) c.330+16C>G (n.330+16C>G) c.144+16C>G (n.144+16C>G) c.2319+16C>G (n.2319+16C>G) c.603+16C>G (n.603+16C>G) | dbSNP |
| 2 | g.29222501G= | CA1241090592 | ALK | c.3450+16C= (n.3450+16C=) c.677+16C= n.327+16C= c.246+16C= (n.246+16C=) c.330+16C= (n.330+16C=) c.144+16C= (n.144+16C=) c.2319+16C= (n.2319+16C=) c.603+16C= (n.603+16C=) | |
| 2 | g.29222502T>A | CA2698809523 | ALK | c.3450+15A>T (n.3450+15A>T) c.677+15A>T n.327+15A>T c.246+15A>T (n.246+15A>T) c.330+15A>T (n.330+15A>T) c.144+15A>T (n.144+15A>T) c.2319+15A>T (n.2319+15A>T) c.603+15A>T (n.603+15A>T) | dbSNP |
| 2 | g.29222502T>C | CA2698809520 | ALK | c.3450+15A>G (n.3450+15A>G) c.677+15A>G n.327+15A>G c.246+15A>G (n.246+15A>G) c.330+15A>G (n.330+15A>G) c.144+15A>G (n.144+15A>G) c.2319+15A>G (n.2319+15A>G) c.603+15A>G (n.603+15A>G) | dbSNP |
| 2 | g.29222502T>G | CA1241090595 | ALK | c.3450+15A>C (n.3450+15A>C) c.677+15A>C n.327+15A>C c.246+15A>C (n.246+15A>C) c.330+15A>C (n.330+15A>C) c.144+15A>C (n.144+15A>C) c.2319+15A>C (n.2319+15A>C) c.603+15A>C (n.603+15A>C) | dbSNP |
| 2 | g.29222502T= | CA1241090594 | ALK | c.3450+15A= (n.3450+15A=) c.677+15A= n.327+15A= c.246+15A= (n.246+15A=) c.330+15A= (n.330+15A=) c.144+15A= (n.144+15A=) c.2319+15A= (n.2319+15A=) c.603+15A= (n.603+15A=) | |
| 2 | g.29222503G>A | CA2580066308 | ALK | c.3450+14C>T (n.3450+14C>T) c.677+14C>T n.327+14C>T c.246+14C>T (n.246+14C>T) c.330+14C>T (n.330+14C>T) c.144+14C>T (n.144+14C>T) c.2319+14C>T (n.2319+14C>T) c.603+14C>T (n.603+14C>T) | ClinVar dbSNP gnomAD v4 |
| 2 | g.29222503G>C | CA2698975621 | ALK | c.3450+14C>G (n.3450+14C>G) c.677+14C>G n.327+14C>G c.246+14C>G (n.246+14C>G) c.330+14C>G (n.330+14C>G) c.144+14C>G (n.144+14C>G) c.2319+14C>G (n.2319+14C>G) c.603+14C>G (n.603+14C>G) | ClinVar dbSNP |
| 2 | g.29222503G>T | CA2698975643 | ALK | c.3450+14C>A (n.3450+14C>A) c.677+14C>A n.327+14C>A c.246+14C>A (n.246+14C>A) c.330+14C>A (n.330+14C>A) c.144+14C>A (n.144+14C>A) c.2319+14C>A (n.2319+14C>A) c.603+14C>A (n.603+14C>A) | dbSNP |
| 2 | g.29222504A>G | CA2698975705 | ALK | c.3450+13T>C (n.3450+13T>C) c.677+13T>C n.327+13T>C c.246+13T>C (n.246+13T>C) c.330+13T>C (n.330+13T>C) c.144+13T>C (n.144+13T>C) c.2319+13T>C (n.2319+13T>C) c.603+13T>C (n.603+13T>C) | dbSNP |
| 2 | g.29222504A>T | CA2698975702 | ALK | c.3450+13T>A (n.3450+13T>A) c.677+13T>A n.327+13T>A c.246+13T>A (n.246+13T>A) c.330+13T>A (n.330+13T>A) c.144+13T>A (n.144+13T>A) c.2319+13T>A (n.2319+13T>A) c.603+13T>A (n.603+13T>A) | dbSNP |
| 2 | g.29222512_29222530dup | CA2580066309 | ALK | c.3445_3450+13dup c.672_677+13dup n.322_327+13dup c.241_246+13dup c.325_330+13dup c.139_144+13dup c.2314_2319+13dup c.598_603+13dup | ClinVar |
| 2 | g.29222505G>A | CA1241090597 | ALK | c.3450+12C>T (n.3450+12C>T) c.677+12C>T n.327+12C>T c.246+12C>T (n.246+12C>T) c.330+12C>T (n.330+12C>T) c.144+12C>T (n.144+12C>T) c.2319+12C>T (n.2319+12C>T) c.603+12C>T (n.603+12C>T) | ClinVar dbSNP gnomAD v4 |
| 2 | g.29222505G= | CA1241090596 | ALK | c.3450+12C= (n.3450+12C=) c.677+12C= n.327+12C= c.246+12C= (n.246+12C=) c.330+12C= (n.330+12C=) c.144+12C= (n.144+12C=) c.2319+12C= (n.2319+12C=) c.603+12C= (n.603+12C=) | |
| 2 | g.29222506C>A | CA2573134536 | ALK | c.3450+11G>T (n.3450+11G>T) c.677+11G>T n.327+11G>T c.246+11G>T (n.246+11G>T) c.330+11G>T (n.330+11G>T) c.144+11G>T (n.144+11G>T) c.2319+11G>T (n.2319+11G>T) c.603+11G>T (n.603+11G>T) | ClinVar dbSNP gnomAD v4 |
| 2 | g.29222506C>G | CA2698975707 | ALK | c.3450+11G>C (n.3450+11G>C) c.677+11G>C n.327+11G>C c.246+11G>C (n.246+11G>C) c.330+11G>C (n.330+11G>C) c.144+11G>C (n.144+11G>C) c.2319+11G>C (n.2319+11G>C) c.603+11G>C (n.603+11G>C) | dbSNP |
| 2 | g.29222506C>T | CA2698975747 | ALK | c.3450+11G>A (n.3450+11G>A) c.677+11G>A n.327+11G>A c.246+11G>A (n.246+11G>A) c.330+11G>A (n.330+11G>A) c.144+11G>A (n.144+11G>A) c.2319+11G>A (n.2319+11G>A) c.603+11G>A (n.603+11G>A) | dbSNP |
| 2 | g.29222507C>A | CA2698975780 | ALK | c.3450+10G>T (n.3450+10G>T) c.677+10G>T n.327+10G>T c.246+10G>T (n.246+10G>T) c.330+10G>T (n.330+10G>T) c.144+10G>T (n.144+10G>T) c.2319+10G>T (n.2319+10G>T) c.603+10G>T (n.603+10G>T) | dbSNP |
| 2 | g.29222507C>G | CA2698975787 | ALK | c.3450+10G>C (n.3450+10G>C) c.677+10G>C n.327+10G>C c.246+10G>C (n.246+10G>C) c.330+10G>C (n.330+10G>C) c.144+10G>C (n.144+10G>C) c.2319+10G>C (n.2319+10G>C) c.603+10G>C (n.603+10G>C) | dbSNP |
| 2 | g.29222507C>T | CA2499215868 | ALK | c.3450+10G>A (n.3450+10G>A) c.677+10G>A n.327+10G>A c.246+10G>A (n.246+10G>A) c.330+10G>A (n.330+10G>A) c.144+10G>A (n.144+10G>A) c.2319+10G>A (n.2319+10G>A) c.603+10G>A (n.603+10G>A) | ClinVar dbSNP gnomAD v4 |
| 2 | g.29222508A>C | CA2698975864 | ALK | c.3450+9T>G (n.3450+9T>G) c.677+9T>G n.327+9T>G c.246+9T>G (n.246+9T>G) c.330+9T>G (n.330+9T>G) c.144+9T>G (n.144+9T>G) c.2319+9T>G (n.2319+9T>G) c.603+9T>G (n.603+9T>G) | dbSNP |
| 2 | g.29222508A>G | CA2698975861 | ALK | c.3450+9T>C (n.3450+9T>C) c.677+9T>C n.327+9T>C c.246+9T>C (n.246+9T>C) c.330+9T>C (n.330+9T>C) c.144+9T>C (n.144+9T>C) c.2319+9T>C (n.2319+9T>C) c.603+9T>C (n.603+9T>C) | dbSNP |
| 2 | g.29222508A>T | CA2658458463 | ALK | c.3450+9T>A (n.3450+9T>A) c.677+9T>A n.327+9T>A c.246+9T>A (n.246+9T>A) c.330+9T>A (n.330+9T>A) c.144+9T>A (n.144+9T>A) c.2319+9T>A (n.2319+9T>A) c.603+9T>A (n.603+9T>A) | dbSNP gnomAD v4 |
| 2 | g.29222509C>G | CA2698975934 | ALK | c.3450+8G>C (n.3450+8G>C) c.677+8G>C n.327+8G>C c.246+8G>C (n.246+8G>C) c.330+8G>C (n.330+8G>C) c.144+8G>C (n.144+8G>C) c.2319+8G>C (n.2319+8G>C) c.603+8G>C (n.603+8G>C) | dbSNP |
| 2 | g.29222512_29222514del | CA2580611259 | ALK | c.3450+6_3450+8del (n.3450+6_3450+8del) c.677+6_677+8del n.327+6_327+8del c.246+6_246+8del (n.246+6_246+8del) c.330+6_330+8del (n.330+6_330+8del) c.144+6_144+8del (n.144+6_144+8del) c.2319+6_2319+8del (n.2319+6_2319+8del) c.603+6_603+8del (n.603+6_603+8del) | ClinVar dbSNP |
| 2 | g.29222510T>A | CA2698806460 | ALK | c.3450+7A>T (n.3450+7A>T) c.677+7A>T n.327+7A>T c.246+7A>T (n.246+7A>T) c.330+7A>T (n.330+7A>T) c.144+7A>T (n.144+7A>T) c.2319+7A>T (n.2319+7A>T) c.603+7A>T (n.603+7A>T) | dbSNP |
| 2 | g.29222510T>C | CA658795691 | ALK | c.3450+7A>G (n.3450+7A>G) c.677+7A>G n.327+7A>G c.246+7A>G (n.246+7A>G) c.330+7A>G (n.330+7A>G) c.144+7A>G (n.144+7A>G) c.2319+7A>G (n.2319+7A>G) c.603+7A>G (n.603+7A>G) | ClinVar dbSNP |
| 2 | g.29222510T= | CA1241090598 | ALK | c.3450+7A= (n.3450+7A=) c.677+7A= n.327+7A= c.246+7A= (n.246+7A=) c.330+7A= (n.330+7A=) c.144+7A= (n.144+7A=) c.2319+7A= (n.2319+7A=) c.603+7A= (n.603+7A=) | |
| 2 | g.29222510_29222511delinsCA | CA2573134538 | ALK | c.3450+6_3450+7delinsTG (n.3450+6_3450+7delinsTG) c.677+6_677+7delinsTG n.327+6_327+7delinsTG c.246+6_246+7delinsTG (n.246+6_246+7delinsTG) c.330+6_330+7delinsTG (n.330+6_330+7delinsTG) c.144+6_144+7delinsTG (n.144+6_144+7delinsTG) c.2319+6_2319+7delinsTG (n.2319+6_2319+7delinsTG) c.603+6_603+7delinsTG (n.603+6_603+7delinsTG) | ClinVar dbSNP |
| 2 | g.29222511T>A | CA2698771024 | ALK | c.3450+6A>T (n.3450+6A>T) c.677+6A>T n.327+6A>T c.246+6A>T (n.246+6A>T) c.330+6A>T (n.330+6A>T) c.144+6A>T (n.144+6A>T) c.2319+6A>T (n.2319+6A>T) c.603+6A>T (n.603+6A>T) | dbSNP |
| 2 | g.29222511T>C | CA1593953 | ALK | c.3450+6A>G (n.3450+6A>G) c.677+6A>G n.327+6A>G c.246+6A>G (n.246+6A>G) c.330+6A>G (n.330+6A>G) c.144+6A>G (n.144+6A>G) c.2319+6A>G (n.2319+6A>G) c.603+6A>G (n.603+6A>G) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 2 | g.29222511T>G | CA2658458468 | ALK | c.3450+6A>C (n.3450+6A>C) c.677+6A>C n.327+6A>C c.246+6A>C (n.246+6A>C) c.330+6A>C (n.330+6A>C) c.144+6A>C (n.144+6A>C) c.2319+6A>C (n.2319+6A>C) c.603+6A>C (n.603+6A>C) | gnomAD v4 |
| 2 | g.29222511T= | CA1241090599 | ALK | c.3450+6A= (n.3450+6A=) c.677+6A= n.327+6A= c.246+6A= (n.246+6A=) c.330+6A= (n.330+6A=) c.144+6A= (n.144+6A=) c.2319+6A= (n.2319+6A=) c.603+6A= (n.603+6A=) | |
| 2 | g.29222512C= | CA1241090600 | ALK | c.3450+5G= (n.3450+5G=) c.677+5G= n.327+5G= c.246+5G= (n.246+5G=) c.330+5G= (n.330+5G=) c.144+5G= (n.144+5G=) c.2319+5G= (n.2319+5G=) c.603+5G= (n.603+5G=) | |
| 2 | g.29222512C>G | CA2698768306 | ALK | c.3450+5G>C (n.3450+5G>C) c.677+5G>C n.327+5G>C c.246+5G>C (n.246+5G>C) c.330+5G>C (n.330+5G>C) c.144+5G>C (n.144+5G>C) c.2319+5G>C (n.2319+5G>C) c.603+5G>C (n.603+5G>C) | dbSNP |
| 2 | g.29222512C>T | CA44631326 | ALK | c.3450+5G>A (n.3450+5G>A) c.677+5G>A n.327+5G>A c.246+5G>A (n.246+5G>A) c.330+5G>A (n.330+5G>A) c.144+5G>A (n.144+5G>A) c.2319+5G>A (n.2319+5G>A) c.603+5G>A (n.603+5G>A) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 2 | g.29222515_29222541del | CA2658458498 | ALK | c.3429_3450+5del c.656_677+5del n.306_327+5del c.225_246+5del c.309_330+5del c.123_144+5del c.2298_2319+5del c.582_603+5del | gnomAD v4 |
| 2 | g.29222513T>A | CA2698823726 | ALK | c.3450+4A>T (n.3450+4A>T) c.677+4A>T n.327+4A>T c.246+4A>T (n.246+4A>T) c.330+4A>T (n.330+4A>T) c.144+4A>T (n.144+4A>T) c.2319+4A>T (n.2319+4A>T) c.603+4A>T (n.603+4A>T) | dbSNP |
| 2 | g.29222513T>C | CA1241090602 | ALK | c.3450+4A>G (n.3450+4A>G) c.677+4A>G n.327+4A>G c.246+4A>G (n.246+4A>G) c.330+4A>G (n.330+4A>G) c.144+4A>G (n.144+4A>G) c.2319+4A>G (n.2319+4A>G) c.603+4A>G (n.603+4A>G) | ClinVar dbSNP |
| 2 | g.29222513T= | CA1241090601 | ALK | c.3450+4A= (n.3450+4A=) c.677+4A= n.327+4A= c.246+4A= (n.246+4A=) c.330+4A= (n.330+4A=) c.144+4A= (n.144+4A=) c.2319+4A= (n.2319+4A=) c.603+4A= (n.603+4A=) | |
| 2 | g.29222514T>C | CA2580066311 | ALK | c.3450+3A>G (n.3450+3A>G) c.677+3A>G n.327+3A>G c.246+3A>G (n.246+3A>G) c.330+3A>G (n.330+3A>G) c.144+3A>G (n.144+3A>G) c.2319+3A>G (n.2319+3A>G) c.603+3A>G (n.603+3A>G) | ClinVar |
| 2 | g.29222515A= | CA1241090603 | ALK | c.3450+2T= (n.3450+2T=) c.677+2T= n.327+2T= c.246+2T= (n.246+2T=) c.330+2T= (n.330+2T=) c.144+2T= (n.144+2T=) c.2319+2T= (n.2319+2T=) c.603+2T= (n.603+2T=) | |
| 2 | g.29222515A>C | CA346463478 | ALK | c.3450+2T>G (n.3450+2T>G) c.677+2T>G n.327+2T>G c.246+2T>G (n.246+2T>G) c.330+2T>G (n.330+2T>G) c.144+2T>G (n.144+2T>G) c.2319+2T>G (n.2319+2T>G) c.603+2T>G (n.603+2T>G) | dbSNP |
| 2 | g.29222515A>G | CA346463484 | ALK | c.3450+2T>C (n.3450+2T>C) c.677+2T>C n.327+2T>C c.246+2T>C (n.246+2T>C) c.330+2T>C (n.330+2T>C) c.144+2T>C (n.144+2T>C) c.2319+2T>C (n.2319+2T>C) c.603+2T>C (n.603+2T>C) | ClinVar dbSNP |
| 2 | g.29222515A>T | CA346463488 | ALK | c.3450+2T>A (n.3450+2T>A) c.677+2T>A n.327+2T>A c.246+2T>A (n.246+2T>A) c.330+2T>A (n.330+2T>A) c.144+2T>A (n.144+2T>A) c.2319+2T>A (n.2319+2T>A) c.603+2T>A (n.603+2T>A) | dbSNP |
| 2 | g.29222516C>A | CA346463492 | ALK | c.3450+1G>T (n.3450+1G>T) c.677+1G>T n.327+1G>T c.246+1G>T (n.246+1G>T) c.330+1G>T (n.330+1G>T) c.144+1G>T (n.144+1G>T) c.2319+1G>T (n.2319+1G>T) c.603+1G>T (n.603+1G>T) | dbSNP gnomAD v4 |
| 2 | g.29222516C= | CA1241090605 | ALK | c.3450+1G= (n.3450+1G=) c.677+1G= n.327+1G= c.246+1G= (n.246+1G=) c.330+1G= (n.330+1G=) c.144+1G= (n.144+1G=) c.2319+1G= (n.2319+1G=) c.603+1G= (n.603+1G=) | |
| 2 | g.29222516C>G | CA346463496 | ALK | c.3450+1G>C (n.3450+1G>C) c.677+1G>C n.327+1G>C c.246+1G>C (n.246+1G>C) c.330+1G>C (n.330+1G>C) c.144+1G>C (n.144+1G>C) c.2319+1G>C (n.2319+1G>C) c.603+1G>C (n.603+1G>C) | dbSNP |
| 2 | g.29222516C>T | CA346463510 | ALK | c.3450+1G>A (n.3450+1G>A) c.677+1G>A n.327+1G>A c.246+1G>A (n.246+1G>A) c.330+1G>A (n.330+1G>A) c.144+1G>A (n.144+1G>A) c.2319+1G>A (n.2319+1G>A) c.603+1G>A (n.603+1G>A) | dbSNP gnomAD v3 gnomAD v4 |
| 2 | g.29222516_29222517delinsAA | CA658795692 | ALK | c.3450_3450+1delinsTT c.677_677+1delinsTT n.327_327+1delinsTT c.246_246+1delinsTT c.330_330+1delinsTT c.144_144+1delinsTT c.2319_2319+1delinsTT c.603_603+1delinsTT | ClinVar dbSNP |
| 2 | g.29222516_29222517delinsCC | CA1241090604 | ALK | c.3450_3450+1delinsGG c.677_677+1delinsGG n.327_327+1delinsGG c.246_246+1delinsGG c.330_330+1delinsGG c.144_144+1delinsGG c.2319_2319+1delinsGG c.603_603+1delinsGG | |
| 2 | g.29222517C>A | CA346463514 | ALK | c.3450G>T (p.Lys1150Asn) c.677G>T n.327G>T c.246G>T (p.Lys82Asn) c.330G>T (p.Lys110Asn) c.144G>T (p.Lys48Asn) c.2319G>T (p.Lys773Asn) c.603G>T (p.Lys201Asn) | dbSNP gnomAD v4 |
| 2 | g.29222517C= | CA1241090606 | ALK | c.3450G= (p.Lys1150=) c.677G= n.327G= c.246G= (p.Lys82=) c.330G= (p.Lys110=) c.144G= (p.Lys48=) c.2319G= (p.Lys773=) c.603G= (p.Lys201=) | |
| 2 | g.29222517C>G | CA346463520 | ALK | c.3450G>C (p.Lys1150Asn) c.677G>C n.327G>C c.246G>C (p.Lys82Asn) c.330G>C (p.Lys110Asn) c.144G>C (p.Lys48Asn) c.2319G>C (p.Lys773Asn) c.603G>C (p.Lys201Asn) | dbSNP |
| 2 | g.29222517C>T | CA425434603 | ALK | c.3450G>A (p.Lys1150=) c.677G>A n.327G>A c.246G>A (p.Lys82=) c.330G>A (p.Lys110=) c.144G>A (p.Lys48=) c.2319G>A (p.Lys773=) c.603G>A (p.Lys201=) | ClinVar dbSNP |
| 2 | g.29222518T>A | CA346463538 | ALK | c.3449A>T (p.Lys1150Met) c.676A>T n.326A>T c.245A>T (p.Lys82Met) c.329A>T (p.Lys110Met) c.143A>T (p.Lys48Met) c.2318A>T (p.Lys773Met) c.602A>T (p.Lys201Met) | dbSNP |
| 2 | g.29222518T>C | CA346463543 | ALK | c.3449A>G (p.Lys1150Arg) c.676A>G n.326A>G c.245A>G (p.Lys82Arg) c.329A>G (p.Lys110Arg) c.143A>G (p.Lys48Arg) c.2318A>G (p.Lys773Arg) c.602A>G (p.Lys201Arg) | dbSNP |
| 2 | g.29222518T>G | CA346463544 | ALK | c.3449A>C (p.Lys1150Thr) c.676A>C n.326A>C c.245A>C (p.Lys82Thr) c.329A>C (p.Lys110Thr) c.143A>C (p.Lys48Thr) c.2318A>C (p.Lys773Thr) c.602A>C (p.Lys201Thr) | ClinVar dbSNP |
| 2 | g.29222519T>A | CA346463546 | ALK | c.3448A>T (p.Lys1150Ter) c.675A>T n.325A>T c.244A>T (p.Lys82Ter) c.328A>T (p.Lys110Ter) c.142A>T (p.Lys48Ter) c.2317A>T (p.Lys773Ter) c.601A>T (p.Lys201Ter) | |
| 2 | g.29222519T>C | CA44631328 | ALK | c.3448A>G (p.Lys1150Glu) c.675A>G n.325A>G c.244A>G (p.Lys82Glu) c.328A>G (p.Lys110Glu) c.142A>G (p.Lys48Glu) c.2317A>G (p.Lys773Glu) c.601A>G (p.Lys201Glu) | dbSNP |
| 2 | g.29222519T>G | CA346463545 | ALK | c.3448A>C (p.Lys1150Gln) c.675A>C n.325A>C c.244A>C (p.Lys82Gln) c.328A>C (p.Lys110Gln) c.142A>C (p.Lys48Gln) c.2317A>C (p.Lys773Gln) c.601A>C (p.Lys201Gln) | |
| 2 | g.29222519T= | CA1241090607 | ALK | c.3448A= (p.Lys1150=) c.675A= n.325A= c.244A= (p.Lys82=) c.328A= (p.Lys110=) c.142A= (p.Lys48=) c.2317A= (p.Lys773=) c.601A= (p.Lys201=) | |
| 2 | g.29222520C>A | CA425434604 | ALK | c.3447G>T (p.Val1149=) c.674G>T n.324G>T c.243G>T (p.Val81=) c.327G>T (p.Val109=) c.141G>T (p.Val47=) c.2316G>T (p.Val772=) c.600G>T (p.Val200=) | dbSNP gnomAD v4 |
| 2 | g.29222520C>G | CA425434605 | ALK | c.3447G>C (p.Val1149=) c.674G>C n.324G>C c.243G>C (p.Val81=) c.327G>C (p.Val109=) c.141G>C (p.Val47=) c.2316G>C (p.Val772=) c.600G>C (p.Val200=) | dbSNP |
| 2 | g.29222520C>T | CA425434606 | ALK | c.3447G>A (p.Val1149=) c.674G>A n.324G>A c.243G>A (p.Val81=) c.327G>A (p.Val109=) c.141G>A (p.Val47=) c.2316G>A (p.Val772=) c.600G>A (p.Val200=) | ClinVar dbSNP gnomAD v4 |
| 2 | g.29222522_29222523del | CA2698976548 | ALK | c.3446_3447del (p.Val1149GlufsTer5) c.673_674del n.323_324del c.242_243del (p.Val81GlufsTer5) c.326_327del (p.Val109GlufsTer5) c.140_141del (p.Val47GlufsTer5) c.2315_2316del (p.Val772GlufsTer5) c.599_600del (p.Val200GlufsTer5) | dbSNP |
| 2 | g.29222521A= | CA1241090608 | ALK | c.3446T= (p.Val1149=) c.673T= n.323T= c.242T= (p.Val81=) c.326T= (p.Val109=) c.140T= (p.Val47=) c.2315T= (p.Val772=) c.599T= (p.Val200=) | |
| 2 | g.29222521A>C | CA44631330 | ALK | c.3446T>G (p.Val1149Gly) c.673T>G n.323T>G c.242T>G (p.Val81Gly) c.326T>G (p.Val109Gly) c.140T>G (p.Val47Gly) c.2315T>G (p.Val772Gly) c.599T>G (p.Val200Gly) | dbSNP |
| 2 | g.29222521A>G | CA346463558 | ALK | c.3446T>C (p.Val1149Ala) c.673T>C n.323T>C c.242T>C (p.Val81Ala) c.326T>C (p.Val109Ala) c.140T>C (p.Val47Ala) c.2315T>C (p.Val772Ala) c.599T>C (p.Val200Ala) | ClinVar |
| 2 | g.29222521A>T | CA346463566 | ALK | c.3446T>A (p.Val1149Glu) c.673T>A n.323T>A c.242T>A (p.Val81Glu) c.326T>A (p.Val109Glu) c.140T>A (p.Val47Glu) c.2315T>A (p.Val772Glu) c.599T>A (p.Val200Glu) | |
| 2 | g.29222522C>A | CA346463574 | ALK | c.3445G>T (p.Val1149Leu) c.672G>T n.322G>T c.241G>T (p.Val81Leu) c.325G>T (p.Val109Leu) c.139G>T (p.Val47Leu) c.2314G>T (p.Val772Leu) c.598G>T (p.Val200Leu) | dbSNP |
| 2 | g.29222522C= | CA1241090609 | ALK | c.3445G= (p.Val1149=) c.672G= n.322G= c.241G= (p.Val81=) c.325G= (p.Val109=) c.139G= (p.Val47=) c.2314G= (p.Val772=) c.598G= (p.Val200=) | |
| 2 | g.29222522C>G | CA346463577 | ALK | c.3445G>C (p.Val1149Leu) c.672G>C n.322G>C c.241G>C (p.Val81Leu) c.325G>C (p.Val109Leu) c.139G>C (p.Val47Leu) c.2314G>C (p.Val772Leu) c.598G>C (p.Val200Leu) | ClinVar dbSNP |
| 2 | g.29222522C>T | CA346463586 | ALK | c.3445G>A (p.Val1149Met) c.672G>A n.322G>A c.241G>A (p.Val81Met) c.325G>A (p.Val109Met) c.139G>A (p.Val47Met) c.2314G>A (p.Val772Met) c.598G>A (p.Val200Met) | ClinVar dbSNP |
| 2 | g.29222523A>C | CA425434607 | ALK | c.3444T>G (p.Ala1148=) c.671T>G n.321T>G c.240T>G (p.Ala80=) c.324T>G (p.Ala108=) c.138T>G (p.Ala46=) c.2313T>G (p.Ala771=) c.597T>G (p.Ala199=) | |
| 2 | g.29222523A>G | CA425434608 | ALK | c.3444T>C (p.Ala1148=) c.671T>C n.321T>C c.240T>C (p.Ala80=) c.324T>C (p.Ala108=) c.138T>C (p.Ala46=) c.2313T>C (p.Ala771=) c.597T>C (p.Ala199=) | dbSNP |
| 2 | g.29222523A>T | CA425434609 | ALK | c.3444T>A (p.Ala1148=) c.671T>A n.321T>A c.240T>A (p.Ala80=) c.324T>A (p.Ala108=) c.138T>A (p.Ala46=) c.2313T>A (p.Ala771=) c.597T>A (p.Ala199=) | dbSNP |
| 2 | g.29222524G>A | CA1593954 | ALK | c.3443C>T (p.Ala1148Val) c.670C>T n.320C>T c.239C>T (p.Ala80Val) c.323C>T (p.Ala108Val) c.137C>T (p.Ala46Val) c.2312C>T (p.Ala771Val) c.596C>T (p.Ala199Val) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 2 | g.29222524G>C | CA346463589 | ALK | c.3443C>G (p.Ala1148Gly) c.670C>G n.320C>G c.239C>G (p.Ala80Gly) c.323C>G (p.Ala108Gly) c.137C>G (p.Ala46Gly) c.2312C>G (p.Ala771Gly) c.596C>G (p.Ala199Gly) | |
| 2 | g.29222524G= | CA1241090610 | ALK | c.3443C= (p.Ala1148=) c.670C= n.320C= c.239C= (p.Ala80=) c.323C= (p.Ala108=) c.137C= (p.Ala46=) c.2312C= (p.Ala771=) c.596C= (p.Ala199=) | |
| 2 | g.29222524G>T | CA346463590 | ALK | c.3443C>A (p.Ala1148Asp) c.670C>A n.320C>A c.239C>A (p.Ala80Asp) c.323C>A (p.Ala108Asp) c.137C>A (p.Ala46Asp) c.2312C>A (p.Ala771Asp) c.596C>A (p.Ala199Asp) | |
| 2 | g.29222525C>A | CA346463591 | ALK | c.3442G>T (p.Ala1148Ser) c.669G>T n.319G>T c.238G>T (p.Ala80Ser) c.322G>T (p.Ala108Ser) c.136G>T (p.Ala46Ser) c.2311G>T (p.Ala771Ser) c.595G>T (p.Ala199Ser) | dbSNP |
| 2 | g.29222525C= | CA1241090611 | ALK | c.3442G= (p.Ala1148=) c.669G= n.319G= c.238G= (p.Ala80=) c.322G= (p.Ala108=) c.136G= (p.Ala46=) c.2311G= (p.Ala771=) c.595G= (p.Ala199=) | |
| 2 | g.29222525C>G | CA346463592 | ALK | c.3442G>C (p.Ala1148Pro) c.669G>C n.319G>C c.238G>C (p.Ala80Pro) c.322G>C (p.Ala108Pro) c.136G>C (p.Ala46Pro) c.2311G>C (p.Ala771Pro) c.595G>C (p.Ala199Pro) | dbSNP |
| 2 | g.29222525C>T | CA346463594 | ALK | c.3442G>A (p.Ala1148Thr) c.669G>A n.319G>A c.238G>A (p.Ala80Thr) c.322G>A (p.Ala108Thr) c.136G>A (p.Ala46Thr) c.2311G>A (p.Ala771Thr) c.595G>A (p.Ala199Thr) | ClinVar dbSNP gnomAD v4 |
| 2 | g.29222526C>A | CA425434612 | ALK | c.3441G>T (p.Val1147=) c.668G>T n.318G>T c.237G>T (p.Val79=) c.321G>T (p.Val107=) c.135G>T (p.Val45=) c.2310G>T (p.Val770=) c.594G>T (p.Val198=) | ClinVar dbSNP gnomAD v4 |
| 2 | g.29222526C= | CA1241090612 | ALK | c.3441G= (p.Val1147=) c.668G= n.318G= c.237G= (p.Val79=) c.321G= (p.Val107=) c.135G= (p.Val45=) c.2310G= (p.Val770=) c.594G= (p.Val198=) | |
| 2 | g.29222526C>G | CA425434613 | ALK | c.3441G>C (p.Val1147=) c.668G>C n.318G>C c.237G>C (p.Val79=) c.321G>C (p.Val107=) c.135G>C (p.Val45=) c.2310G>C (p.Val770=) c.594G>C (p.Val198=) | dbSNP |
| 2 | g.29222526C>T | CA425434611 | ALK | c.3441G>A (p.Val1147=) c.668G>A n.318G>A c.237G>A (p.Val79=) c.321G>A (p.Val107=) c.135G>A (p.Val45=) c.2310G>A (p.Val770=) c.594G>A (p.Val198=) | dbSNP |
| 2 | g.29222527A= | CA1241090613 | ALK | c.3440T= (p.Val1147=) c.667T= n.317T= c.236T= (p.Val79=) c.320T= (p.Val107=) c.134T= (p.Val45=) c.2309T= (p.Val770=) c.593T= (p.Val198=) | |
| 2 | g.29222527A>C | CA346463606 | ALK | c.3440T>G (p.Val1147Gly) c.667T>G n.317T>G c.236T>G (p.Val79Gly) c.320T>G (p.Val107Gly) c.134T>G (p.Val45Gly) c.2309T>G (p.Val770Gly) c.593T>G (p.Val198Gly) | dbSNP |
| 2 | g.29222527A>G | CA346463609 | ALK | c.3440T>C (p.Val1147Ala) c.667T>C n.317T>C c.236T>C (p.Val79Ala) c.320T>C (p.Val107Ala) c.134T>C (p.Val45Ala) c.2309T>C (p.Val770Ala) c.593T>C (p.Val198Ala) | ClinVar dbSNP |
| 2 | g.29222527A>T | CA346463600 | ALK | c.3440T>A (p.Val1147Glu) c.667T>A n.317T>A c.236T>A (p.Val79Glu) c.320T>A (p.Val107Glu) c.134T>A (p.Val45Glu) c.2309T>A (p.Val770Glu) c.593T>A (p.Val198Glu) | dbSNP |
| 2 | g.29222528C>A | CA346463611 | ALK | c.3439G>T (p.Val1147Leu) c.666G>T n.316G>T c.235G>T (p.Val79Leu) c.319G>T (p.Val107Leu) c.133G>T (p.Val45Leu) c.2308G>T (p.Val770Leu) c.592G>T (p.Val198Leu) | |
| 2 | g.29222528C= | CA1241090614 | ALK | c.3439G= (p.Val1147=) c.666G= n.316G= c.235G= (p.Val79=) c.319G= (p.Val107=) c.133G= (p.Val45=) c.2308G= (p.Val770=) c.592G= (p.Val198=) | |
| 2 | g.29222528C>G | CA346463612 | ALK | c.3439G>C (p.Val1147Leu) c.666G>C n.316G>C c.235G>C (p.Val79Leu) c.319G>C (p.Val107Leu) c.133G>C (p.Val45Leu) c.2308G>C (p.Val770Leu) c.592G>C (p.Val198Leu) | ClinVar dbSNP gnomAD v4 |
| 2 | g.29222528C>T | CA346463613 | ALK | c.3439G>A (p.Val1147Met) c.666G>A n.316G>A c.235G>A (p.Val79Met) c.319G>A (p.Val107Met) c.133G>A (p.Val45Met) c.2308G>A (p.Val770Met) c.592G>A (p.Val198Met) | dbSNP gnomAD v2 gnomAD v4 |
| 2 | g.29222529T>A | CA346463616 | ALK | c.3438A>T (p.Gln1146His) c.665A>T n.315A>T c.234A>T (p.Gln78His) c.318A>T (p.Gln106His) c.132A>T (p.Gln44His) c.2307A>T (p.Gln769His) c.591A>T (p.Gln197His) | dbSNP |
| 2 | g.29222529T>C | CA1593955 | ALK | c.3438A>G (p.Gln1146=) c.665A>G n.315A>G c.234A>G (p.Gln78=) c.318A>G (p.Gln106=) c.132A>G (p.Gln44=) c.2307A>G (p.Gln769=) c.591A>G (p.Gln197=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 2 | g.29222529T>G | CA346463620 | ALK | c.3438A>C (p.Gln1146His) c.665A>C n.315A>C c.234A>C (p.Gln78His) c.318A>C (p.Gln106His) c.132A>C (p.Gln44His) c.2307A>C (p.Gln769His) c.591A>C (p.Gln197His) | dbSNP gnomAD v2 gnomAD v4 |
| 2 | g.29222529T= | CA1241090615 | ALK | c.3438A= (p.Gln1146=) c.665A= n.315A= c.234A= (p.Gln78=) c.318A= (p.Gln106=) c.132A= (p.Gln44=) c.2307A= (p.Gln769=) c.591A= (p.Gln197=) | |
| 2 | g.29222530T>A | CA346463625 | ALK | c.3437A>T (p.Gln1146Leu) c.664A>T n.314A>T c.233A>T (p.Gln78Leu) c.317A>T (p.Gln106Leu) c.131A>T (p.Gln44Leu) c.2306A>T (p.Gln769Leu) c.590A>T (p.Gln197Leu) | ClinVar dbSNP |
| 2 | g.29222530T>C | CA346463626 | ALK | c.3437A>G (p.Gln1146Arg) c.664A>G n.314A>G c.233A>G (p.Gln78Arg) c.317A>G (p.Gln106Arg) c.131A>G (p.Gln44Arg) c.2306A>G (p.Gln769Arg) c.590A>G (p.Gln197Arg) | |
| 2 | g.29222530T>G | CA346463627 | ALK | c.3437A>C (p.Gln1146Pro) c.664A>C n.314A>C c.233A>C (p.Gln78Pro) c.317A>C (p.Gln106Pro) c.131A>C (p.Gln44Pro) c.2306A>C (p.Gln769Pro) c.590A>C (p.Gln197Pro) | |
| 2 | g.29222531G>A | CA346463628 | ALK | c.3436C>T (p.Gln1146Ter) c.663C>T n.313C>T c.232C>T (p.Gln78Ter) c.316C>T (p.Gln106Ter) c.130C>T (p.Gln44Ter) c.2305C>T (p.Gln769Ter) c.589C>T (p.Gln197Ter) | gnomAD v4 |
| 2 | g.29222531G>C | CA346463629 | ALK | c.3436C>G (p.Gln1146Glu) c.663C>G n.313C>G c.232C>G (p.Gln78Glu) c.316C>G (p.Gln106Glu) c.130C>G (p.Gln44Glu) c.2305C>G (p.Gln769Glu) c.589C>G (p.Gln197Glu) | |
| 2 | g.29222531G>T | CA346463633 | ALK | c.3436C>A (p.Gln1146Lys) c.663C>A n.313C>A c.232C>A (p.Gln78Lys) c.316C>A (p.Gln106Lys) c.130C>A (p.Gln44Lys) c.2305C>A (p.Gln769Lys) c.589C>A (p.Gln197Lys) | ClinVar dbSNP gnomAD v4 |
| 2 | g.29222532C>A | CA425434616 | ALK | c.3435G>T (p.Leu1145=) c.662G>T n.312G>T c.231G>T (p.Leu77=) c.315G>T (p.Leu105=) c.129G>T (p.Leu43=) c.2304G>T (p.Leu768=) c.588G>T (p.Leu196=) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 2 | g.29222532C= | CA1241090616 | ALK | c.3435G= (p.Leu1145=) c.662G= n.312G= c.231G= (p.Leu77=) c.315G= (p.Leu105=) c.129G= (p.Leu43=) c.2304G= (p.Leu768=) c.588G= (p.Leu196=) | |
| 2 | g.29222532C>G | CA425434617 | ALK | c.3435G>C (p.Leu1145=) c.662G>C n.312G>C c.231G>C (p.Leu77=) c.315G>C (p.Leu105=) c.129G>C (p.Leu43=) c.2304G>C (p.Leu768=) c.588G>C (p.Leu196=) | dbSNP |
| 2 | g.29222532C>T | CA425434619 | ALK | c.3435G>A (p.Leu1145=) c.662G>A n.312G>A c.231G>A (p.Leu77=) c.315G>A (p.Leu105=) c.129G>A (p.Leu43=) c.2304G>A (p.Leu768=) c.588G>A (p.Leu196=) | ClinVar dbSNP gnomAD v4 |
| 2 | g.29222533A>C | CA346463641 | ALK | c.3434T>G (p.Leu1145Arg) c.661T>G n.311T>G c.230T>G (p.Leu77Arg) c.314T>G (p.Leu105Arg) c.128T>G (p.Leu43Arg) c.2303T>G (p.Leu768Arg) c.587T>G (p.Leu196Arg) | |
| 2 | g.29222533A>G | CA346463649 | ALK | c.3434T>C (p.Leu1145Pro) c.661T>C n.311T>C c.230T>C (p.Leu77Pro) c.314T>C (p.Leu105Pro) c.128T>C (p.Leu43Pro) c.2303T>C (p.Leu768Pro) c.587T>C (p.Leu196Pro) | |
| 2 | g.29222533A>T | CA346463637 | ALK | c.3434T>A (p.Leu1145Gln) c.661T>A n.311T>A c.230T>A (p.Leu77Gln) c.314T>A (p.Leu105Gln) c.128T>A (p.Leu43Gln) c.2303T>A (p.Leu768Gln) c.587T>A (p.Leu196Gln) | |
| 2 | g.29222534G>A | CA425434621 | ALK | c.3433C>T (p.Leu1145=) c.660C>T n.310C>T c.229C>T (p.Leu77=) c.313C>T (p.Leu105=) c.127C>T (p.Leu43=) c.2302C>T (p.Leu768=) c.586C>T (p.Leu196=) | ClinVar dbSNP |
| 2 | g.29222534G>C | CA346463653 | ALK | c.3433C>G (p.Leu1145Val) c.660C>G n.310C>G c.229C>G (p.Leu77Val) c.313C>G (p.Leu105Val) c.127C>G (p.Leu43Val) c.2302C>G (p.Leu768Val) c.586C>G (p.Leu196Val) | dbSNP |
| 2 | g.29222534G>T | CA346463654 | ALK | c.3433C>A (p.Leu1145Met) c.660C>A n.310C>A c.229C>A (p.Leu77Met) c.313C>A (p.Leu105Met) c.127C>A (p.Leu43Met) c.2302C>A (p.Leu768Met) c.586C>A (p.Leu196Met) | dbSNP |
| 2 | g.29222538dup | CA2749317736 | ALK | c.3433dup (p.Leu1145ProfsTer10) c.660dup n.310dup c.229dup (p.Leu77ProfsTer10) c.313dup (p.Leu105ProfsTer10) c.127dup (p.Leu43ProfsTer10) c.2302dup (p.Leu768ProfsTer10) c.586dup (p.Leu196ProfsTer10) | |
| 2 | g.29222538del | CA425434622 | ALK | c.3433del (p.Leu1145CysfsTer5) c.660del n.310del c.229del (p.Leu77CysfsTer5) c.313del (p.Leu105CysfsTer5) c.127del (p.Leu43CysfsTer5) c.2302del (p.Leu768CysfsTer5) c.586del (p.Leu196CysfsTer5) | COSMIC |
| 2 | g.29222535G>A | CA44631341 | ALK | c.3432C>T (p.Pro1144=) c.659C>T n.309C>T c.228C>T (p.Pro76=) c.312C>T (p.Pro104=) c.126C>T (p.Pro42=) c.2301C>T (p.Pro767=) c.585C>T (p.Pro195=) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 2 | g.29222535G>C | CA425434623 | ALK | c.3432C>G (p.Pro1144=) c.659C>G n.309C>G c.228C>G (p.Pro76=) c.312C>G (p.Pro104=) c.126C>G (p.Pro42=) c.2301C>G (p.Pro767=) c.585C>G (p.Pro195=) | dbSNP |
| 2 | g.29222535G= | CA1241090617 | ALK | c.3432C= (p.Pro1144=) c.659C= n.309C= c.228C= (p.Pro76=) c.312C= (p.Pro104=) c.126C= (p.Pro42=) c.2301C= (p.Pro767=) c.585C= (p.Pro195=) | |
| 2 | g.29222535G>T | CA425434624 | ALK | c.3432C>A (p.Pro1144=) c.659C>A n.309C>A c.228C>A (p.Pro76=) c.312C>A (p.Pro104=) c.126C>A (p.Pro42=) c.2301C>A (p.Pro767=) c.585C>A (p.Pro195=) | dbSNP |
| 2 | g.29222536G>A | CA346463665 | ALK | c.3431C>T (p.Pro1144Leu) c.658C>T n.308C>T c.227C>T (p.Pro76Leu) c.311C>T (p.Pro104Leu) c.125C>T (p.Pro42Leu) c.2300C>T (p.Pro767Leu) c.584C>T (p.Pro195Leu) | ClinVar dbSNP |
| 2 | g.29222536G>C | CA346463670 | ALK | c.3431C>G (p.Pro1144Arg) c.658C>G n.308C>G c.227C>G (p.Pro76Arg) c.311C>G (p.Pro104Arg) c.125C>G (p.Pro42Arg) c.2300C>G (p.Pro767Arg) c.584C>G (p.Pro195Arg) | ClinVar dbSNP |
| 2 | g.29222536G= | CA1241090618 | ALK | c.3431C= (p.Pro1144=) c.658C= n.308C= c.227C= (p.Pro76=) c.311C= (p.Pro104=) c.125C= (p.Pro42=) c.2300C= (p.Pro767=) c.584C= (p.Pro195=) | |
| 2 | g.29222536G>T | CA346463671 | ALK | c.3431C>A (p.Pro1144His) c.658C>A n.308C>A c.227C>A (p.Pro76His) c.311C>A (p.Pro104His) c.125C>A (p.Pro42His) c.2300C>A (p.Pro767His) c.584C>A (p.Pro195His) | dbSNP |
| 2 | g.29222537G>A | CA346463678 | ALK | c.3430C>T (p.Pro1144Ser) c.657C>T n.307C>T c.226C>T (p.Pro76Ser) c.310C>T (p.Pro104Ser) c.124C>T (p.Pro42Ser) c.2299C>T (p.Pro767Ser) c.583C>T (p.Pro195Ser) | ClinVar dbSNP |
| 2 | g.29222537G>C | CA346463672 | ALK | c.3430C>G (p.Pro1144Ala) c.657C>G n.307C>G c.226C>G (p.Pro76Ala) c.310C>G (p.Pro104Ala) c.124C>G (p.Pro42Ala) c.2299C>G (p.Pro767Ala) c.583C>G (p.Pro195Ala) | dbSNP |
| 2 | g.29222537G>T | CA346463676 | ALK | c.3430C>A (p.Pro1144Thr) c.657C>A n.307C>A c.226C>A (p.Pro76Thr) c.310C>A (p.Pro104Thr) c.124C>A (p.Pro42Thr) c.2299C>A (p.Pro767Thr) c.583C>A (p.Pro195Thr) | |
| 2 | g.29222538G>A | CA425434627 | ALK | c.3429C>T (p.Ser1143=) c.656C>T n.306C>T c.225C>T (p.Ser75=) c.309C>T (p.Ser103=) c.123C>T (p.Ser41=) c.2298C>T (p.Ser766=) c.582C>T (p.Ser194=) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 2 | g.29222538G>C | CA346463681 | ALK | c.3429C>G (p.Ser1143Arg) c.656C>G n.306C>G c.225C>G (p.Ser75Arg) c.309C>G (p.Ser103Arg) c.123C>G (p.Ser41Arg) c.2298C>G (p.Ser766Arg) c.582C>G (p.Ser194Arg) | dbSNP |
| 2 | g.29222538G= | CA1241090619 | ALK | c.3429C= (p.Ser1143=) c.656C= n.306C= c.225C= (p.Ser75=) c.309C= (p.Ser103=) c.123C= (p.Ser41=) c.2298C= (p.Ser766=) c.582C= (p.Ser194=) | |
| 2 | g.29222538G>T | CA346463683 | ALK | c.3429C>A (p.Ser1143Arg) c.656C>A n.306C>A c.225C>A (p.Ser75Arg) c.309C>A (p.Ser103Arg) c.123C>A (p.Ser41Arg) c.2298C>A (p.Ser766Arg) c.582C>A (p.Ser194Arg) | |
| 2 | g.29222539C>A | CA346463685 | ALK | c.3428G>T (p.Ser1143Ile) c.655G>T n.305G>T c.224G>T (p.Ser75Ile) c.308G>T (p.Ser103Ile) c.122G>T (p.Ser41Ile) c.2297G>T (p.Ser766Ile) c.581G>T (p.Ser194Ile) | ClinVar dbSNP |
| 2 | g.29222539C= | CA1241090620 | ALK | c.3428G= (p.Ser1143=) c.655G= n.305G= c.224G= (p.Ser75=) c.308G= (p.Ser103=) c.122G= (p.Ser41=) c.2297G= (p.Ser766=) c.581G= (p.Ser194=) | |
| 2 | g.29222539C>G | CA346463690 | ALK | c.3428G>C (p.Ser1143Thr) c.655G>C n.305G>C c.224G>C (p.Ser75Thr) c.308G>C (p.Ser103Thr) c.122G>C (p.Ser41Thr) c.2297G>C (p.Ser766Thr) c.581G>C (p.Ser194Thr) | dbSNP |
| 2 | g.29222539C>T | CA346463700 | ALK | c.3428G>A (p.Ser1143Asn) c.655G>A n.305G>A c.224G>A (p.Ser75Asn) c.308G>A (p.Ser103Asn) c.122G>A (p.Ser41Asn) c.2297G>A (p.Ser766Asn) c.581G>A (p.Ser194Asn) | dbSNP |
| 2 | g.29222540T>A | CA346463708 | ALK | c.3427A>T (p.Ser1143Cys) c.654A>T n.304A>T c.223A>T (p.Ser75Cys) c.307A>T (p.Ser103Cys) c.121A>T (p.Ser41Cys) c.2296A>T (p.Ser766Cys) c.580A>T (p.Ser194Cys) | dbSNP |
| 2 | g.29222540T>C | CA346463707 | ALK | c.3427A>G (p.Ser1143Gly) c.654A>G n.304A>G c.223A>G (p.Ser75Gly) c.307A>G (p.Ser103Gly) c.121A>G (p.Ser41Gly) c.2296A>G (p.Ser766Gly) c.580A>G (p.Ser194Gly) | dbSNP |
| 2 | g.29222540T>G | CA346463706 | ALK | c.3427A>C (p.Ser1143Arg) c.654A>C n.304A>C c.223A>C (p.Ser75Arg) c.307A>C (p.Ser103Arg) c.121A>C (p.Ser41Arg) c.2296A>C (p.Ser766Arg) c.580A>C (p.Ser194Arg) | |
| 2 | g.29222541T>A | CA425434630 | ALK | c.3426A>T (p.Pro1142=) c.653A>T n.303A>T c.222A>T (p.Pro74=) c.306A>T (p.Pro102=) c.120A>T (p.Pro40=) c.2295A>T (p.Pro765=) c.579A>T (p.Pro193=) | |
| 2 | g.29222541T>C | CA425434632 | ALK | c.3426A>G (p.Pro1142=) c.653A>G n.303A>G c.222A>G (p.Pro74=) c.306A>G (p.Pro102=) c.120A>G (p.Pro40=) c.2295A>G (p.Pro765=) c.579A>G (p.Pro193=) | |
| 2 | g.29222541T>G | CA425434635 | ALK | c.3426A>C (p.Pro1142=) c.653A>C n.303A>C c.222A>C (p.Pro74=) c.306A>C (p.Pro102=) c.120A>C (p.Pro40=) c.2295A>C (p.Pro765=) c.579A>C (p.Pro193=) | COSMIC |
| 2 | g.29222542G>A | CA346463709 | ALK | c.3425C>T (p.Pro1142Leu) c.652C>T n.302C>T c.221C>T (p.Pro74Leu) c.305C>T (p.Pro102Leu) c.119C>T (p.Pro40Leu) c.2294C>T (p.Pro765Leu) c.578C>T (p.Pro193Leu) | ClinVar dbSNP |
| 2 | g.29222542G>C | CA346463710 | ALK | c.3425C>G (p.Pro1142Arg) c.652C>G n.302C>G c.221C>G (p.Pro74Arg) c.305C>G (p.Pro102Arg) c.119C>G (p.Pro40Arg) c.2294C>G (p.Pro765Arg) c.578C>G (p.Pro193Arg) | |
| 2 | g.29222542G>T | CA346463714 | ALK | c.3425C>A (p.Pro1142Gln) c.652C>A n.302C>A c.221C>A (p.Pro74Gln) c.305C>A (p.Pro102Gln) c.119C>A (p.Pro40Gln) c.2294C>A (p.Pro765Gln) c.578C>A (p.Pro193Gln) | dbSNP gnomAD v4 |
| 2 | g.29222543G>A | CA346463716 | ALK | c.3424C>T (p.Pro1142Ser) c.651C>T n.301C>T c.220C>T (p.Pro74Ser) c.304C>T (p.Pro102Ser) c.118C>T (p.Pro40Ser) c.2293C>T (p.Pro765Ser) c.577C>T (p.Pro193Ser) | dbSNP |
| 2 | g.29222543G>C | CA346463717 | ALK | c.3424C>G (p.Pro1142Ala) c.651C>G n.301C>G c.220C>G (p.Pro74Ala) c.304C>G (p.Pro102Ala) c.118C>G (p.Pro40Ala) c.2293C>G (p.Pro765Ala) c.577C>G (p.Pro193Ala) | dbSNP |
| 2 | g.29222543G= | CA1241090621 | ALK | c.3424C= (p.Pro1142=) c.651C= n.301C= c.220C= (p.Pro74=) c.304C= (p.Pro102=) c.118C= (p.Pro40=) c.2293C= (p.Pro765=) c.577C= (p.Pro193=) | |
| 2 | g.29222543G>T | CA346463718 | ALK | c.3424C>A (p.Pro1142Thr) c.651C>A n.301C>A c.220C>A (p.Pro74Thr) c.304C>A (p.Pro102Thr) c.118C>A (p.Pro40Thr) c.2293C>A (p.Pro765Thr) c.577C>A (p.Pro193Thr) | dbSNP gnomAD v3 gnomAD v4 |
| 2 | g.29222544G>A | CA1593956 | ALK | c.3423C>T (p.Asp1141=) c.650C>T n.300C>T c.219C>T (p.Asp73=) c.303C>T (p.Asp101=) c.117C>T (p.Asp39=) c.2292C>T (p.Asp764=) c.576C>T (p.Asp192=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 2 | g.29222544G>C | CA346463732 | ALK | c.3423C>G (p.Asp1141Glu) c.650C>G n.300C>G c.219C>G (p.Asp73Glu) c.303C>G (p.Asp101Glu) c.117C>G (p.Asp39Glu) c.2292C>G (p.Asp764Glu) c.576C>G (p.Asp192Glu) | dbSNP |
| 2 | g.29222544G= | CA1241090622 | ALK | c.3423C= (p.Asp1141=) c.650C= n.300C= c.219C= (p.Asp73=) c.303C= (p.Asp101=) c.117C= (p.Asp39=) c.2292C= (p.Asp764=) c.576C= (p.Asp192=) | |
| 2 | g.29222544G>T | CA346463719 | ALK | c.3423C>A (p.Asp1141Glu) c.650C>A n.300C>A c.219C>A (p.Asp73Glu) c.303C>A (p.Asp101Glu) c.117C>A (p.Asp39Glu) c.2292C>A (p.Asp764Glu) c.576C>A (p.Asp192Glu) | |
| 2 | g.29222545T>A | CA346463746 | ALK | c.3422A>T (p.Asp1141Val) c.649A>T n.299A>T c.218A>T (p.Asp73Val) c.302A>T (p.Asp101Val) c.116A>T (p.Asp39Val) c.2291A>T (p.Asp764Val) c.575A>T (p.Asp192Val) | dbSNP |
| 2 | g.29222545T>C | CA346463757 | ALK | c.3422A>G (p.Asp1141Gly) c.649A>G n.299A>G c.218A>G (p.Asp73Gly) c.302A>G (p.Asp101Gly) c.116A>G (p.Asp39Gly) c.2291A>G (p.Asp764Gly) c.575A>G (p.Asp192Gly) | |
| 2 | g.29222545T>G | CA346463760 | ALK | c.3422A>C (p.Asp1141Ala) c.649A>C n.299A>C c.218A>C (p.Asp73Ala) c.302A>C (p.Asp101Ala) c.116A>C (p.Asp39Ala) c.2291A>C (p.Asp764Ala) c.575A>C (p.Asp192Ala) | dbSNP |
| 2 | g.29222546C>A | CA346463763 | ALK | c.3421G>T (p.Asp1141Tyr) c.648G>T n.298G>T c.217G>T (p.Asp73Tyr) c.301G>T (p.Asp101Tyr) c.115G>T (p.Asp39Tyr) c.2290G>T (p.Asp764Tyr) c.574G>T (p.Asp192Tyr) | dbSNP |
| 2 | g.29222546C= | CA1241090623 | ALK | c.3421G= (p.Asp1141=) c.648G= n.298G= c.217G= (p.Asp73=) c.301G= (p.Asp101=) c.115G= (p.Asp39=) c.2290G= (p.Asp764=) c.574G= (p.Asp192=) | |
| 2 | g.29222546C>G | CA346463770 | ALK | c.3421G>C (p.Asp1141His) c.648G>C n.298G>C c.217G>C (p.Asp73His) c.301G>C (p.Asp101His) c.115G>C (p.Asp39His) c.2290G>C (p.Asp764His) c.574G>C (p.Asp192His) | dbSNP |
| 2 | g.29222546C>T | CA1593957 | ALK | c.3421G>A (p.Asp1141Asn) c.648G>A n.298G>A c.217G>A (p.Asp73Asn) c.301G>A (p.Asp101Asn) c.115G>A (p.Asp39Asn) c.2290G>A (p.Asp764Asn) c.574G>A (p.Asp192Asn) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 2 | g.29222547G>A | CA1593958 | ALK | c.3420C>T (p.Asn1140=) c.647C>T n.297C>T c.216C>T (p.Asn72=) c.300C>T (p.Asn100=) c.114C>T (p.Asn38=) c.2289C>T (p.Asn763=) c.573C>T (p.Asn191=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 2 | g.29222547G>C | CA1593959 | ALK | c.3420C>G (p.Asn1140Lys) c.647C>G n.297C>G c.216C>G (p.Asn72Lys) c.300C>G (p.Asn100Lys) c.114C>G (p.Asn38Lys) c.2289C>G (p.Asn763Lys) c.573C>G (p.Asn191Lys) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 2 | g.29222547G= | CA1241090624 | ALK | c.3420C= (p.Asn1140=) c.647C= n.297C= c.216C= (p.Asn72=) c.300C= (p.Asn100=) c.114C= (p.Asn38=) c.2289C= (p.Asn763=) c.573C= (p.Asn191=) | |
| 2 | g.29222547G>T | CA346463783 | ALK | c.3420C>A (p.Asn1140Lys) c.647C>A n.297C>A c.216C>A (p.Asn72Lys) c.300C>A (p.Asn100Lys) c.114C>A (p.Asn38Lys) c.2289C>A (p.Asn763Lys) c.573C>A (p.Asn191Lys) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 2 | g.29222548T>A | CA346463805 | ALK | c.3419A>T (p.Asn1140Ile) c.646A>T n.296A>T c.215A>T (p.Asn72Ile) c.299A>T (p.Asn100Ile) c.113A>T (p.Asn38Ile) c.2288A>T (p.Asn763Ile) c.572A>T (p.Asn191Ile) | dbSNP |
| 2 | g.29222548T>C | CA346463807 | ALK | c.3419A>G (p.Asn1140Ser) c.646A>G n.296A>G c.215A>G (p.Asn72Ser) c.299A>G (p.Asn100Ser) c.113A>G (p.Asn38Ser) c.2288A>G (p.Asn763Ser) c.572A>G (p.Asn191Ser) | ClinVar dbSNP |
| 2 | g.29222548T>G | CA346463810 | ALK | c.3419A>C (p.Asn1140Thr) c.646A>C n.296A>C c.215A>C (p.Asn72Thr) c.299A>C (p.Asn100Thr) c.113A>C (p.Asn38Thr) c.2288A>C (p.Asn763Thr) c.572A>C (p.Asn191Thr) | dbSNP |
| 2 | g.29222549T>A | CA346463818 | ALK | c.3418A>T (p.Asn1140Tyr) c.645A>T n.295A>T c.214A>T (p.Asn72Tyr) c.298A>T (p.Asn100Tyr) c.112A>T (p.Asn38Tyr) c.2287A>T (p.Asn763Tyr) c.571A>T (p.Asn191Tyr) | |
| 2 | g.29222549T>C | CA346463821 | ALK | c.3418A>G (p.Asn1140Asp) c.645A>G n.295A>G c.214A>G (p.Asn72Asp) c.298A>G (p.Asn100Asp) c.112A>G (p.Asn38Asp) c.2287A>G (p.Asn763Asp) c.571A>G (p.Asn191Asp) | |
| 2 | g.29222549T>G | CA346463824 | ALK | c.3418A>C (p.Asn1140His) c.645A>C n.295A>C c.214A>C (p.Asn72His) c.298A>C (p.Asn100His) c.112A>C (p.Asn38His) c.2287A>C (p.Asn763His) c.571A>C (p.Asn191His) | |
| 2 | g.29222550G>A | CA425434642 | ALK | c.3417C>T (p.Pro1139=) c.644C>T n.294C>T c.213C>T (p.Pro71=) c.297C>T (p.Pro99=) c.111C>T (p.Pro37=) c.2286C>T (p.Pro762=) c.570C>T (p.Pro190=) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 2 | g.29222550G>C | CA425434643 | ALK | c.3417C>G (p.Pro1139=) c.644C>G n.294C>G c.213C>G (p.Pro71=) c.297C>G (p.Pro99=) c.111C>G (p.Pro37=) c.2286C>G (p.Pro762=) c.570C>G (p.Pro190=) | dbSNP |
| 2 | g.29222550G= | CA1241090625 | ALK | c.3417C= (p.Pro1139=) c.644C= n.294C= c.213C= (p.Pro71=) c.297C= (p.Pro99=) c.111C= (p.Pro37=) c.2286C= (p.Pro762=) c.570C= (p.Pro190=) | |
| 2 | g.29222550G>T | CA425434644 | ALK | c.3417C>A (p.Pro1139=) c.644C>A n.294C>A c.213C>A (p.Pro71=) c.297C>A (p.Pro99=) c.111C>A (p.Pro37=) c.2286C>A (p.Pro762=) c.570C>A (p.Pro190=) | dbSNP |
| 2 | g.29222551G>A | CA1593960 | ALK | c.3416C>T (p.Pro1139Leu) c.643C>T n.293C>T c.212C>T (p.Pro71Leu) c.296C>T (p.Pro99Leu) c.110C>T (p.Pro37Leu) c.2285C>T (p.Pro762Leu) c.569C>T (p.Pro190Leu) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 2 | g.29222551G>C | CA346463830 | ALK | c.3416C>G (p.Pro1139Arg) c.643C>G n.293C>G c.212C>G (p.Pro71Arg) c.296C>G (p.Pro99Arg) c.110C>G (p.Pro37Arg) c.2285C>G (p.Pro762Arg) c.569C>G (p.Pro190Arg) | dbSNP |
| 2 | g.29222551G= | CA1241090626 | ALK | c.3416C= (p.Pro1139=) c.643C= n.293C= c.212C= (p.Pro71=) c.296C= (p.Pro99=) c.110C= (p.Pro37=) c.2285C= (p.Pro762=) c.569C= (p.Pro190=) | |
| 2 | g.29222551G>T | CA346463832 | ALK | c.3416C>A (p.Pro1139His) c.643C>A n.293C>A c.212C>A (p.Pro71His) c.296C>A (p.Pro99His) c.110C>A (p.Pro37His) c.2285C>A (p.Pro762His) c.569C>A (p.Pro190His) | dbSNP gnomAD v4 |
| 2 | g.29222552G>A | CA346463835 | ALK | c.3415C>T (p.Pro1139Ser) c.642C>T n.292C>T c.211C>T (p.Pro71Ser) c.295C>T (p.Pro99Ser) c.109C>T (p.Pro37Ser) c.2284C>T (p.Pro762Ser) c.568C>T (p.Pro190Ser) | dbSNP |
| 2 | g.29222552G>C | CA346463837 | ALK | c.3415C>G (p.Pro1139Ala) c.642C>G n.292C>G c.211C>G (p.Pro71Ala) c.295C>G (p.Pro99Ala) c.109C>G (p.Pro37Ala) c.2284C>G (p.Pro762Ala) c.568C>G (p.Pro190Ala) | dbSNP |
| 2 | g.29222552G>T | CA346463841 | ALK | c.3415C>A (p.Pro1139Thr) c.642C>A n.292C>A c.211C>A (p.Pro71Thr) c.295C>A (p.Pro99Thr) c.109C>A (p.Pro37Thr) c.2284C>A (p.Pro762Thr) c.568C>A (p.Pro190Thr) | dbSNP |
| 2 | g.29222553C>A | CA346463844 | ALK | c.3414G>T (p.Met1138Ile) c.641G>T n.291G>T c.210G>T (p.Met70Ile) c.294G>T (p.Met98Ile) c.108G>T (p.Met36Ile) c.2283G>T (p.Met761Ile) c.567G>T (p.Met189Ile) | dbSNP |
| 2 | g.29222553C= | CA1241090627 | ALK | c.3414G= (p.Met1138=) c.641G= n.291G= c.210G= (p.Met70=) c.294G= (p.Met98=) c.108G= (p.Met36=) c.2283G= (p.Met761=) c.567G= (p.Met189=) | |
| 2 | g.29222553C>G | CA346463846 | ALK | c.3414G>C (p.Met1138Ile) c.641G>C n.291G>C c.210G>C (p.Met70Ile) c.294G>C (p.Met98Ile) c.108G>C (p.Met36Ile) c.2283G>C (p.Met761Ile) c.567G>C (p.Met189Ile) | dbSNP |
| 2 | g.29222553C>T | CA1593961 | ALK | c.3414G>A (p.Met1138Ile) c.641G>A n.291G>A c.210G>A (p.Met70Ile) c.294G>A (p.Met98Ile) c.108G>A (p.Met36Ile) c.2283G>A (p.Met761Ile) c.567G>A (p.Met189Ile) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 2 | g.29222554A>C | CA346463850 | ALK | c.3413T>G (p.Met1138Arg) c.640T>G n.290T>G c.209T>G (p.Met70Arg) c.293T>G (p.Met98Arg) c.107T>G (p.Met36Arg) c.2282T>G (p.Met761Arg) c.566T>G (p.Met189Arg) | dbSNP |
| 2 | g.29222554A>G | CA346463851 | ALK | c.3413T>C (p.Met1138Thr) c.640T>C n.290T>C c.209T>C (p.Met70Thr) c.293T>C (p.Met98Thr) c.107T>C (p.Met36Thr) c.2282T>C (p.Met761Thr) c.566T>C (p.Met189Thr) | ClinVar dbSNP |
| 2 | g.29222554A>T | CA346463859 | ALK | c.3413T>A (p.Met1138Lys) c.640T>A n.290T>A c.209T>A (p.Met70Lys) c.293T>A (p.Met98Lys) c.107T>A (p.Met36Lys) c.2282T>A (p.Met761Lys) c.566T>A (p.Met189Lys) | dbSNP COSMIC |
| 2 | g.29222555T>A | CA346463863 | ALK | c.3412A>T (p.Met1138Leu) c.639A>T n.289A>T c.208A>T (p.Met70Leu) c.292A>T (p.Met98Leu) c.106A>T (p.Met36Leu) c.2281A>T (p.Met761Leu) c.565A>T (p.Met189Leu) | dbSNP |
| 2 | g.29222555T>C | CA346463877 | ALK | c.3412A>G (p.Met1138Val) c.639A>G n.289A>G c.208A>G (p.Met70Val) c.292A>G (p.Met98Val) c.106A>G (p.Met36Val) c.2281A>G (p.Met761Val) c.565A>G (p.Met189Val) | dbSNP |
| 2 | g.29222555T>G | CA346463883 | ALK | c.3412A>C (p.Met1138Leu) c.639A>C n.289A>C c.208A>C (p.Met70Leu) c.292A>C (p.Met98Leu) c.106A>C (p.Met36Leu) c.2281A>C (p.Met761Leu) c.565A>C (p.Met189Leu) | dbSNP |
| 2 | g.29222556T>A | CA425434646 | ALK | c.3411A>T (p.Gly1137=) c.638A>T n.288A>T c.207A>T (p.Gly69=) c.291A>T (p.Gly97=) c.105A>T (p.Gly35=) c.2280A>T (p.Gly760=) c.564A>T (p.Gly188=) | |
| 2 | g.29222556T>C | CA425434648 | ALK | c.3411A>G (p.Gly1137=) c.638A>G n.288A>G c.207A>G (p.Gly69=) c.291A>G (p.Gly97=) c.105A>G (p.Gly35=) c.2280A>G (p.Gly760=) c.564A>G (p.Gly188=) | |
| 2 | g.29222556T>G | CA425434649 | ALK | c.3411A>C (p.Gly1137=) c.638A>C n.288A>C c.207A>C (p.Gly69=) c.291A>C (p.Gly97=) c.105A>C (p.Gly35=) c.2280A>C (p.Gly760=) c.564A>C (p.Gly188=) | |
| 2 | g.29222556_29222564delinsTCCGGACAC | CA1241090628 | ALK | c.3403_3411delinsGTGTCCGGA (p.Val1135=) c.630_638delinsGTGTCCGGA n.280_288delinsGTGTCCGGA c.199_207delinsGTGTCCGGA (p.Val67=) c.283_291delinsGTGTCCGGA (p.Val95=) c.97_105delinsGTGTCCGGA (p.Val33=) c.2272_2280delinsGTGTCCGGA (p.Val758=) c.556_564delinsGTGTCCGGA (p.Val186=) | |
| 2 | g.29222557C>A | CA346463885 | ALK | c.3410G>T (p.Gly1137Val) c.637G>T n.287G>T c.206G>T (p.Gly69Val) c.290G>T (p.Gly97Val) c.104G>T (p.Gly35Val) c.2279G>T (p.Gly760Val) c.563G>T (p.Gly188Val) | dbSNP |
| 2 | g.29222557C= | CA1241090629 | ALK | c.3410G= (p.Gly1137=) c.637G= n.287G= c.206G= (p.Gly69=) c.290G= (p.Gly97=) c.104G= (p.Gly35=) c.2279G= (p.Gly760=) c.563G= (p.Gly188=) | |
| 2 | g.29222557C>G | CA346463892 | ALK | c.3410G>C (p.Gly1137Ala) c.637G>C n.287G>C c.206G>C (p.Gly69Ala) c.290G>C (p.Gly97Ala) c.104G>C (p.Gly35Ala) c.2279G>C (p.Gly760Ala) c.563G>C (p.Gly188Ala) | dbSNP |
| 2 | g.29222557C>T | CA346463894 | ALK | c.3410G>A (p.Gly1137Glu) c.637G>A n.287G>A c.206G>A (p.Gly69Glu) c.290G>A (p.Gly97Glu) c.104G>A (p.Gly35Glu) c.2279G>A (p.Gly760Glu) c.563G>A (p.Gly188Glu) | ClinVar dbSNP |
| 2 | g.29222557_29222558delinsTT | CA645528803 | ALK | c.3409_3410delinsAA (p.Gly1137Lys) c.636_637delinsAA n.286_287delinsAA c.205_206delinsAA (p.Gly69Lys) c.289_290delinsAA (p.Gly97Lys) c.103_104delinsAA (p.Gly35Lys) c.2278_2279delinsAA (p.Gly760Lys) c.562_563delinsAA (p.Gly188Lys) | COSMIC |
| 2 | g.29222558_29222565del | CA531766937 | ALK | c.3403_3410del (p.Val1135AsnfsTer17) c.630_637del n.280_287del c.199_206del (p.Val67AsnfsTer17) c.283_290del (p.Val95AsnfsTer17) c.97_104del (p.Val33AsnfsTer17) c.2272_2279del (p.Val758AsnfsTer17) c.556_563del (p.Val186AsnfsTer17) | dbSNP gnomAD v2 gnomAD v4 |
| 2 | g.29222558C>A | CA346463898 | ALK | c.3409G>T (p.Gly1137Ter) c.636G>T n.286G>T c.205G>T (p.Gly69Ter) c.289G>T (p.Gly97Ter) c.103G>T (p.Gly35Ter) c.2278G>T (p.Gly760Ter) c.562G>T (p.Gly188Ter) | dbSNP |
| 2 | g.29222558C= | CA1241090630 | ALK | c.3409G= (p.Gly1137=) c.636G= n.286G= c.205G= (p.Gly69=) c.289G= (p.Gly97=) c.103G= (p.Gly35=) c.2278G= (p.Gly760=) c.562G= (p.Gly188=) | |
| 2 | g.29222558C>G | CA346463901 | ALK | c.3409G>C (p.Gly1137Arg) c.636G>C n.286G>C c.205G>C (p.Gly69Arg) c.289G>C (p.Gly97Arg) c.103G>C (p.Gly35Arg) c.2278G>C (p.Gly760Arg) c.562G>C (p.Gly188Arg) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 2 | g.29222558C>T | CA1593962 | ALK | c.3409G>A (p.Gly1137Arg) c.636G>A n.286G>A c.205G>A (p.Gly69Arg) c.289G>A (p.Gly97Arg) c.103G>A (p.Gly35Arg) c.2278G>A (p.Gly760Arg) c.562G>A (p.Gly188Arg) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 2 | g.29222559G>A | CA1593963 | ALK | c.3408C>T (p.Ser1136=) c.635C>T n.285C>T c.204C>T (p.Ser68=) c.288C>T (p.Ser96=) c.102C>T (p.Ser34=) c.2277C>T (p.Ser759=) c.561C>T (p.Ser187=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 2 | g.29222559G>C | CA425434653 | ALK | c.3408C>G (p.Ser1136=) c.635C>G n.285C>G c.204C>G (p.Ser68=) c.288C>G (p.Ser96=) c.102C>G (p.Ser34=) c.2277C>G (p.Ser759=) c.561C>G (p.Ser187=) | dbSNP |
| 2 | g.29222559G= | CA1241090631 | ALK | c.3408C= (p.Ser1136=) c.635C= n.285C= c.204C= (p.Ser68=) c.288C= (p.Ser96=) c.102C= (p.Ser34=) c.2277C= (p.Ser759=) c.561C= (p.Ser187=) | |
| 2 | g.29222559G>T | CA425434655 | ALK | c.3408C>A (p.Ser1136=) c.635C>A n.285C>A c.204C>A (p.Ser68=) c.288C>A (p.Ser96=) c.102C>A (p.Ser34=) c.2277C>A (p.Ser759=) c.561C>A (p.Ser187=) | dbSNP |
| 2 | g.29222560G>A | CA346463925 | ALK | c.3407C>T (p.Ser1136Phe) c.634C>T n.284C>T c.203C>T (p.Ser68Phe) c.287C>T (p.Ser96Phe) c.101C>T (p.Ser34Phe) c.2276C>T (p.Ser759Phe) c.560C>T (p.Ser187Phe) | dbSNP |
| 2 | g.29222560G>C | CA346463919 | ALK | c.3407C>G (p.Ser1136Cys) c.634C>G n.284C>G c.203C>G (p.Ser68Cys) c.287C>G (p.Ser96Cys) c.101C>G (p.Ser34Cys) c.2276C>G (p.Ser759Cys) c.560C>G (p.Ser187Cys) | dbSNP |
| 2 | g.29222560G>T | CA346463922 | ALK | c.3407C>A (p.Ser1136Tyr) c.634C>A n.284C>A c.203C>A (p.Ser68Tyr) c.287C>A (p.Ser96Tyr) c.101C>A (p.Ser34Tyr) c.2276C>A (p.Ser759Tyr) c.560C>A (p.Ser187Tyr) | dbSNP gnomAD v4 |
| 2 | g.29222561A= | CA1241090632 | ALK | c.3406T= (p.Ser1136=) c.633T= n.283T= c.202T= (p.Ser68=) c.286T= (p.Ser96=) c.100T= (p.Ser34=) c.2275T= (p.Ser759=) c.559T= (p.Ser187=) | |
| 2 | g.29222561A>C | CA346463927 | ALK | c.3406T>G (p.Ser1136Ala) c.633T>G n.283T>G c.202T>G (p.Ser68Ala) c.286T>G (p.Ser96Ala) c.100T>G (p.Ser34Ala) c.2275T>G (p.Ser759Ala) c.559T>G (p.Ser187Ala) | ClinVar dbSNP gnomAD v4 |
| 2 | g.29222561A>G | CA346463928 | ALK | c.3406T>C (p.Ser1136Pro) c.633T>C n.283T>C c.202T>C (p.Ser68Pro) c.286T>C (p.Ser96Pro) c.100T>C (p.Ser34Pro) c.2275T>C (p.Ser759Pro) c.559T>C (p.Ser187Pro) | dbSNP |
| 2 | g.29222561A>T | CA346463930 | ALK | c.3406T>A (p.Ser1136Thr) c.633T>A n.283T>A c.202T>A (p.Ser68Thr) c.286T>A (p.Ser96Thr) c.100T>A (p.Ser34Thr) c.2275T>A (p.Ser759Thr) c.559T>A (p.Ser187Thr) | dbSNP |
| 2 | g.29222567_29222581del | CA2573134539 | ALK | c.3392_3406del (p.Tyr1131_Val1135del) c.619_633del n.269_283del c.188_202del (p.Tyr63_Val67del) c.272_286del (p.Tyr91_Val95del) c.86_100del (p.Tyr29_Val33del) c.2261_2275del (p.Tyr754_Val758del) c.545_559del (p.Tyr182_Val186del) | ClinVar dbSNP |
| 2 | g.29222562C>A | CA425434657 | ALK | c.3405G>T (p.Val1135=) c.632G>T n.282G>T c.201G>T (p.Val67=) c.285G>T (p.Val95=) c.99G>T (p.Val33=) c.2274G>T (p.Val758=) c.558G>T (p.Val186=) | dbSNP |
| 2 | g.29222562C= | CA1241090633 | ALK | c.3405G= (p.Val1135=) c.632G= n.282G= c.201G= (p.Val67=) c.285G= (p.Val95=) c.99G= (p.Val33=) c.2274G= (p.Val758=) c.558G= (p.Val186=) | |
| 2 | g.29222562C>G | CA425434658 | ALK | c.3405G>C (p.Val1135=) c.632G>C n.282G>C c.201G>C (p.Val67=) c.285G>C (p.Val95=) c.99G>C (p.Val33=) c.2274G>C (p.Val758=) c.558G>C (p.Val186=) | dbSNP |
| 2 | g.29222562C>T | CA44631363 | ALK | c.3405G>A (p.Val1135=) c.632G>A n.282G>A c.201G>A (p.Val67=) c.285G>A (p.Val95=) c.99G>A (p.Val33=) c.2274G>A (p.Val758=) c.558G>A (p.Val186=) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 2 | g.29222563A>C | CA346463937 | ALK | c.3404T>G (p.Val1135Gly) c.631T>G n.281T>G c.200T>G (p.Val67Gly) c.284T>G (p.Val95Gly) c.98T>G (p.Val33Gly) c.2273T>G (p.Val758Gly) c.557T>G (p.Val186Gly) | |
| 2 | g.29222563A>G | CA346463941 | ALK | c.3404T>C (p.Val1135Ala) c.631T>C n.281T>C c.200T>C (p.Val67Ala) c.284T>C (p.Val95Ala) c.98T>C (p.Val33Ala) c.2273T>C (p.Val758Ala) c.557T>C (p.Val186Ala) | ClinVar dbSNP gnomAD v4 |
| 2 | g.29222563A>T | CA346463943 | ALK | c.3404T>A (p.Val1135Glu) c.631T>A n.281T>A c.200T>A (p.Val67Glu) c.284T>A (p.Val95Glu) c.98T>A (p.Val33Glu) c.2273T>A (p.Val758Glu) c.557T>A (p.Val186Glu) | dbSNP COSMIC |
| 2 | g.29222564C>A | CA346463944 | ALK | c.3403G>T (p.Val1135Leu) c.630G>T n.280G>T c.199G>T (p.Val67Leu) c.283G>T (p.Val95Leu) c.97G>T (p.Val33Leu) c.2272G>T (p.Val758Leu) c.556G>T (p.Val186Leu) | ClinVar dbSNP gnomAD v4 |
| 2 | g.29222564C>G | CA346463945 | ALK | c.3403G>C (p.Val1135Leu) c.630G>C n.280G>C c.199G>C (p.Val67Leu) c.283G>C (p.Val95Leu) c.97G>C (p.Val33Leu) c.2272G>C (p.Val758Leu) c.556G>C (p.Val186Leu) | dbSNP |
| 2 | g.29222564C>T | CA346463947 | ALK | c.3403G>A (p.Val1135Met) c.630G>A n.280G>A c.199G>A (p.Val67Met) c.283G>A (p.Val95Met) c.97G>A (p.Val33Met) c.2272G>A (p.Val758Met) c.556G>A (p.Val186Met) | dbSNP gnomAD v4 |
| 2 | g.29222565C>A | CA346463949 | ALK | c.3402G>T (p.Gln1134His) c.629G>T n.279G>T c.198G>T (p.Gln66His) c.282G>T (p.Gln94His) c.96G>T (p.Gln32His) c.2271G>T (p.Gln757His) c.555G>T (p.Gln185His) | dbSNP |
| 2 | g.29222565C>G | CA346463953 | ALK | c.3402G>C (p.Gln1134His) c.629G>C n.279G>C c.198G>C (p.Gln66His) c.282G>C (p.Gln94His) c.96G>C (p.Gln32His) c.2271G>C (p.Gln757His) c.555G>C (p.Gln185His) | dbSNP |
| 2 | g.29222565C>T | CA425434663 | ALK | c.3402G>A (p.Gln1134=) c.629G>A n.279G>A c.198G>A (p.Gln66=) c.282G>A (p.Gln94=) c.96G>A (p.Gln32=) c.2271G>A (p.Gln757=) c.555G>A (p.Gln185=) | ClinVar dbSNP |
| 2 | g.29222566T>A | CA346463956 | ALK | c.3401A>T (p.Gln1134Leu) c.628A>T n.278A>T c.197A>T (p.Gln66Leu) c.281A>T (p.Gln94Leu) c.95A>T (p.Gln32Leu) c.2270A>T (p.Gln757Leu) c.554A>T (p.Gln185Leu) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 2 | g.29222566T>C | CA346463957 | ALK | c.3401A>G (p.Gln1134Arg) c.628A>G n.278A>G c.197A>G (p.Gln66Arg) c.281A>G (p.Gln94Arg) c.95A>G (p.Gln32Arg) c.2270A>G (p.Gln757Arg) c.554A>G (p.Gln185Arg) | ClinVar dbSNP gnomAD v4 |
| 2 | g.29222566T>G | CA346463955 | ALK | c.3401A>C (p.Gln1134Pro) c.628A>C n.278A>C c.197A>C (p.Gln66Pro) c.281A>C (p.Gln94Pro) c.95A>C (p.Gln32Pro) c.2270A>C (p.Gln757Pro) c.554A>C (p.Gln185Pro) | |
| 2 | g.29222566T= | CA1241090634 | ALK | c.3401A= (p.Gln1134=) c.628A= n.278A= c.197A= (p.Gln66=) c.281A= (p.Gln94=) c.95A= (p.Gln32=) c.2270A= (p.Gln757=) c.554A= (p.Gln185=) | |
| 2 | g.29222567G>A | CA346463960 | ALK | c.3400C>T (p.Gln1134Ter) c.627C>T n.277C>T c.196C>T (p.Gln66Ter) c.280C>T (p.Gln94Ter) c.94C>T (p.Gln32Ter) c.2269C>T (p.Gln757Ter) c.553C>T (p.Gln185Ter) | dbSNP |
| 2 | g.29222567G>C | CA346463958 | ALK | c.3400C>G (p.Gln1134Glu) c.627C>G n.277C>G c.196C>G (p.Gln66Glu) c.280C>G (p.Gln94Glu) c.94C>G (p.Gln32Glu) c.2269C>G (p.Gln757Glu) c.553C>G (p.Gln185Glu) | dbSNP |
| 2 | g.29222567G>T | CA346463962 | ALK | c.3400C>A (p.Gln1134Lys) c.627C>A n.277C>A c.196C>A (p.Gln66Lys) c.280C>A (p.Gln94Lys) c.94C>A (p.Gln32Lys) c.2269C>A (p.Gln757Lys) c.553C>A (p.Gln185Lys) | dbSNP |
| 2 | g.29222567_29222568delinsAA | CA645528804 | ALK | c.3399_3400delinsTT (p.Gly1134Ter) c.626_627delinsTT n.276_277delinsTT c.195_196delinsTT (p.Gly66Ter) c.279_280delinsTT (p.Gly94Ter) c.93_94delinsTT (p.Gly32Ter) c.2268_2269delinsTT (p.Gly757Ter) c.552_553delinsTT (p.Gly185Ter) | COSMIC |
| 2 | g.29222568G>A | CA425434669 | ALK | c.3399C>T (p.Gly1133=) c.626C>T n.276C>T c.195C>T (p.Gly65=) c.279C>T (p.Gly93=) c.93C>T (p.Gly31=) c.2268C>T (p.Gly756=) c.552C>T (p.Gly184=) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 2 | g.29222568G>C | CA425434668 | ALK | c.3399C>G (p.Gly1133=) c.626C>G n.276C>G c.195C>G (p.Gly65=) c.279C>G (p.Gly93=) c.93C>G (p.Gly31=) c.2268C>G (p.Gly756=) c.552C>G (p.Gly184=) | dbSNP |
| 2 | g.29222568G= | CA1241090635 | ALK | c.3399C= (p.Gly1133=) c.626C= n.276C= c.195C= (p.Gly65=) c.279C= (p.Gly93=) c.93C= (p.Gly31=) c.2268C= (p.Gly756=) c.552C= (p.Gly184=) | |
| 2 | g.29222568G>T | CA425434667 | ALK | c.3399C>A (p.Gly1133=) c.626C>A n.276C>A c.195C>A (p.Gly65=) c.279C>A (p.Gly93=) c.93C>A (p.Gly31=) c.2268C>A (p.Gly756=) c.552C>A (p.Gly184=) | dbSNP |
| 2 | g.29222569C>A | CA1593964 | ALK | c.3398G>T (p.Gly1133Val) c.625G>T n.275G>T c.194G>T (p.Gly65Val) c.278G>T (p.Gly93Val) c.92G>T (p.Gly31Val) c.2267G>T (p.Gly756Val) c.551G>T (p.Gly184Val) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 2 | g.29222569C= | CA1241090636 | ALK | c.3398G= (p.Gly1133=) c.625G= n.275G= c.194G= (p.Gly65=) c.278G= (p.Gly93=) c.92G= (p.Gly31=) c.2267G= (p.Gly756=) c.551G= (p.Gly184=) | |
| 2 | g.29222569C>G | CA346463966 | ALK | c.3398G>C (p.Gly1133Ala) c.625G>C n.275G>C c.194G>C (p.Gly65Ala) c.278G>C (p.Gly93Ala) c.92G>C (p.Gly31Ala) c.2267G>C (p.Gly756Ala) c.551G>C (p.Gly184Ala) | dbSNP gnomAD v3 gnomAD v4 |
| 2 | g.29222569C>T | CA346463965 | ALK | c.3398G>A (p.Gly1133Asp) c.625G>A n.275G>A c.194G>A (p.Gly65Asp) c.278G>A (p.Gly93Asp) c.92G>A (p.Gly31Asp) c.2267G>A (p.Gly756Asp) c.551G>A (p.Gly184Asp) | dbSNP gnomAD v4 |
| 2 | g.29222570C>A | CA346463969 | ALK | c.3397G>T (p.Gly1133Cys) c.624G>T n.274G>T c.193G>T (p.Gly65Cys) c.277G>T (p.Gly93Cys) c.91G>T (p.Gly31Cys) c.2266G>T (p.Gly756Cys) c.550G>T (p.Gly184Cys) | |
| 2 | g.29222570C>G | CA346463984 | ALK | c.3397G>C (p.Gly1133Arg) c.624G>C n.274G>C c.193G>C (p.Gly65Arg) c.277G>C (p.Gly93Arg) c.91G>C (p.Gly31Arg) c.2266G>C (p.Gly756Arg) c.550G>C (p.Gly184Arg) | dbSNP |
| 2 | g.29222570C>T | CA346463972 | ALK | c.3397G>A (p.Gly1133Ser) c.624G>A n.274G>A c.193G>A (p.Gly65Ser) c.277G>A (p.Gly93Ser) c.91G>A (p.Gly31Ser) c.2266G>A (p.Gly756Ser) c.550G>A (p.Gly184Ser) | dbSNP |
| 2 | g.29222571T>A | CA346463987 | ALK | c.3396A>T (p.Glu1132Asp) c.623A>T n.273A>T c.192A>T (p.Glu64Asp) c.276A>T (p.Glu92Asp) c.90A>T (p.Glu30Asp) c.2265A>T (p.Glu755Asp) c.549A>T (p.Glu183Asp) | dbSNP |
| 2 | g.29222571T>C | CA425434674 | ALK | c.3396A>G (p.Glu1132=) c.623A>G n.273A>G c.192A>G (p.Glu64=) c.276A>G (p.Glu92=) c.90A>G (p.Glu30=) c.2265A>G (p.Glu755=) c.549A>G (p.Glu183=) | dbSNP |
| 2 | g.29222571T>G | CA346463998 | ALK | c.3396A>C (p.Glu1132Asp) c.623A>C n.273A>C c.192A>C (p.Glu64Asp) c.276A>C (p.Glu92Asp) c.90A>C (p.Glu30Asp) c.2265A>C (p.Glu755Asp) c.549A>C (p.Glu183Asp) | |
| 2 | g.29222572T>A | CA346463999 | ALK | c.3395A>T (p.Glu1132Val) c.622A>T n.272A>T c.191A>T (p.Glu64Val) c.275A>T (p.Glu92Val) c.89A>T (p.Glu30Val) c.2264A>T (p.Glu755Val) c.548A>T (p.Glu183Val) | dbSNP |
| 2 | g.29222572T>C | CA346464002 | ALK | c.3395A>G (p.Glu1132Gly) c.622A>G n.272A>G c.191A>G (p.Glu64Gly) c.275A>G (p.Glu92Gly) c.89A>G (p.Glu30Gly) c.2264A>G (p.Glu755Gly) c.548A>G (p.Glu183Gly) | dbSNP |
| 2 | g.29222572T>G | CA346464016 | ALK | c.3395A>C (p.Glu1132Ala) c.622A>C n.272A>C c.191A>C (p.Glu64Ala) c.275A>C (p.Glu92Ala) c.89A>C (p.Glu30Ala) c.2264A>C (p.Glu755Ala) c.548A>C (p.Glu183Ala) | |
| 2 | g.29222572_29222573delinsTC | CA1241090637 | ALK | c.3394_3395delinsGA (p.Glu1132=) c.621_622delinsGA n.271_272delinsGA c.190_191delinsGA (p.Glu64=) c.274_275delinsGA (p.Glu92=) c.88_89delinsGA (p.Glu30=) c.2263_2264delinsGA (p.Glu755=) c.547_548delinsGA (p.Glu183=) | |
| 2 | g.29222573del | CA916500685 | ALK | c.3394del (p.Glu1132LysfsTer18) c.621del n.271del c.190del (p.Glu64LysfsTer18) c.274del (p.Glu92LysfsTer18) c.88del (p.Glu30LysfsTer18) c.2263del (p.Glu755LysfsTer18) c.547del (p.Glu183LysfsTer18) | dbSNP gnomAD v4 |
| 2 | g.29222573C>A | CA346464020 | ALK | c.3394G>T (p.Glu1132Ter) c.621G>T n.271G>T c.190G>T (p.Glu64Ter) c.274G>T (p.Glu92Ter) c.88G>T (p.Glu30Ter) c.2263G>T (p.Glu755Ter) c.547G>T (p.Glu183Ter) | gnomAD v4 |
| 2 | g.29222573C>G | CA346464024 | ALK | c.3394G>C (p.Glu1132Gln) c.621G>C n.271G>C c.190G>C (p.Glu64Gln) c.274G>C (p.Glu92Gln) c.88G>C (p.Glu30Gln) c.2263G>C (p.Glu755Gln) c.547G>C (p.Glu183Gln) | |
| 2 | g.29222573C>T | CA346464027 | ALK | c.3394G>A (p.Glu1132Lys) c.621G>A n.271G>A c.190G>A (p.Glu64Lys) c.274G>A (p.Glu92Lys) c.88G>A (p.Glu30Lys) c.2263G>A (p.Glu755Lys) c.547G>A (p.Glu183Lys) | ClinVar dbSNP gnomAD v4 COSMIC |
| 2 | g.29222574A>C | CA346464030 | ALK | c.3393T>G (p.Tyr1131Ter) c.620T>G n.270T>G c.189T>G (p.Tyr63Ter) c.273T>G (p.Tyr91Ter) c.87T>G (p.Tyr29Ter) c.2262T>G (p.Tyr754Ter) c.546T>G (p.Tyr182Ter) | dbSNP |
| 2 | g.29222574A>G | CA425434681 | ALK | c.3393T>C (p.Tyr1131=) c.620T>C n.270T>C c.189T>C (p.Tyr63=) c.273T>C (p.Tyr91=) c.87T>C (p.Tyr29=) c.2262T>C (p.Tyr754=) c.546T>C (p.Tyr182=) | ClinVar dbSNP |
| 2 | g.29222574A>T | CA346464035 | ALK | c.3393T>A (p.Tyr1131Ter) c.620T>A n.270T>A c.189T>A (p.Tyr63Ter) c.273T>A (p.Tyr91Ter) c.87T>A (p.Tyr29Ter) c.2262T>A (p.Tyr754Ter) c.546T>A (p.Tyr182Ter) | dbSNP |
| 2 | g.29222575T>A | CA346464038 | ALK | c.3392A>T (p.Tyr1131Phe) c.619A>T n.269A>T c.188A>T (p.Tyr63Phe) c.272A>T (p.Tyr91Phe) c.86A>T (p.Tyr29Phe) c.2261A>T (p.Tyr754Phe) c.545A>T (p.Tyr182Phe) | dbSNP |
| 2 | g.29222575T>C | CA346464043 | ALK | c.3392A>G (p.Tyr1131Cys) c.619A>G n.269A>G c.188A>G (p.Tyr63Cys) c.272A>G (p.Tyr91Cys) c.86A>G (p.Tyr29Cys) c.2261A>G (p.Tyr754Cys) c.545A>G (p.Tyr182Cys) | dbSNP |
| 2 | g.29222575T>G | CA346464046 | ALK | c.3392A>C (p.Tyr1131Ser) c.619A>C n.269A>C c.188A>C (p.Tyr63Ser) c.272A>C (p.Tyr91Ser) c.86A>C (p.Tyr29Ser) c.2261A>C (p.Tyr754Ser) c.545A>C (p.Tyr182Ser) | |
| 2 | g.29222576A= | CA1241090638 | ALK | c.3391T= (p.Tyr1131=) c.618T= n.268T= c.187T= (p.Tyr63=) c.271T= (p.Tyr91=) c.85T= (p.Tyr29=) c.2260T= (p.Tyr754=) c.544T= (p.Tyr182=) | |
| 2 | g.29222576A>C | CA346464050 | ALK | c.3391T>G (p.Tyr1131Asp) c.618T>G n.268T>G c.187T>G (p.Tyr63Asp) c.271T>G (p.Tyr91Asp) c.85T>G (p.Tyr29Asp) c.2260T>G (p.Tyr754Asp) c.544T>G (p.Tyr182Asp) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 2 | g.29222576A>G | CA346464051 | ALK | c.3391T>C (p.Tyr1131His) c.618T>C n.268T>C c.187T>C (p.Tyr63His) c.271T>C (p.Tyr91His) c.85T>C (p.Tyr29His) c.2260T>C (p.Tyr754His) c.544T>C (p.Tyr182His) | dbSNP |
| 2 | g.29222576A>T | CA346464053 | ALK | c.3391T>A (p.Tyr1131Asn) c.618T>A n.268T>A c.187T>A (p.Tyr63Asn) c.271T>A (p.Tyr91Asn) c.85T>A (p.Tyr29Asn) c.2260T>A (p.Tyr754Asn) c.544T>A (p.Tyr182Asn) | dbSNP |
| 2 | g.29222577C>A | CA425434685 | ALK | c.3390G>T (p.Val1130=) c.617G>T n.267G>T c.186G>T (p.Val62=) c.270G>T (p.Val90=) c.84G>T (p.Val28=) c.2259G>T (p.Val753=) c.543G>T (p.Val181=) | dbSNP |
| 2 | g.29222577C= | CA1241090639 | ALK | c.3390G= (p.Val1130=) c.617G= n.267G= c.186G= (p.Val62=) c.270G= (p.Val90=) c.84G= (p.Val28=) c.2259G= (p.Val753=) c.543G= (p.Val181=) | |
| 2 | g.29222577C>G | CA425434686 | ALK | c.3390G>C (p.Val1130=) c.617G>C n.267G>C c.186G>C (p.Val62=) c.270G>C (p.Val90=) c.84G>C (p.Val28=) c.2259G>C (p.Val753=) c.543G>C (p.Val181=) | dbSNP |
| 2 | g.29222577C>T | CA425434687 | ALK | c.3390G>A (p.Val1130=) c.617G>A n.267G>A c.186G>A (p.Val62=) c.270G>A (p.Val90=) c.84G>A (p.Val28=) c.2259G>A (p.Val753=) c.543G>A (p.Val181=) | ClinVar dbSNP gnomAD v4 |
| 2 | g.29222578A>C | CA346464057 | ALK | c.3389T>G (p.Val1130Gly) c.616T>G n.266T>G c.185T>G (p.Val62Gly) c.269T>G (p.Val90Gly) c.83T>G (p.Val28Gly) c.2258T>G (p.Val753Gly) c.542T>G (p.Val181Gly) | dbSNP |
| 2 | g.29222578A>G | CA346464065 | ALK | c.3389T>C (p.Val1130Ala) c.616T>C n.266T>C c.185T>C (p.Val62Ala) c.269T>C (p.Val90Ala) c.83T>C (p.Val28Ala) c.2258T>C (p.Val753Ala) c.542T>C (p.Val181Ala) | |
| 2 | g.29222578A>T | CA346464060 | ALK | c.3389T>A (p.Val1130Glu) c.616T>A n.266T>A c.185T>A (p.Val62Glu) c.269T>A (p.Val90Glu) c.83T>A (p.Val28Glu) c.2258T>A (p.Val753Glu) c.542T>A (p.Val181Glu) | dbSNP |
| 2 | g.29222579C>A | CA16610897 | ALK | c.3388G>T (p.Val1130Leu) c.615G>T n.265G>T c.184G>T (p.Val62Leu) c.268G>T (p.Val90Leu) c.82G>T (p.Val28Leu) c.2257G>T (p.Val753Leu) c.541G>T (p.Val181Leu) | ClinVar dbSNP gnomAD v4 |
| 2 | g.29222579C= | CA1241090640 | ALK | c.3388G= (p.Val1130=) c.615G= n.265G= c.184G= (p.Val62=) c.268G= (p.Val90=) c.82G= (p.Val28=) c.2257G= (p.Val753=) c.541G= (p.Val181=) | |
| 2 | g.29222579C>G | CA346464070 | ALK | c.3388G>C (p.Val1130Leu) c.615G>C n.265G>C c.184G>C (p.Val62Leu) c.268G>C (p.Val90Leu) c.82G>C (p.Val28Leu) c.2257G>C (p.Val753Leu) c.541G>C (p.Val181Leu) | dbSNP |
| 2 | g.29222579C>T | CA346464075 | ALK | c.3388G>A (p.Val1130Met) c.615G>A n.265G>A c.184G>A (p.Val62Met) c.268G>A (p.Val90Met) c.82G>A (p.Val28Met) c.2257G>A (p.Val753Met) c.541G>A (p.Val181Met) | ClinVar dbSNP |
| 2 | g.29222580C>A | CA346464080 | ALK | c.3387G>T (p.Glu1129Asp) c.614G>T n.264G>T c.183G>T (p.Glu61Asp) c.267G>T (p.Glu89Asp) c.81G>T (p.Glu27Asp) c.2256G>T (p.Glu752Asp) c.540G>T (p.Glu180Asp) | ClinVar dbSNP |
| 2 | g.29222580C= | CA1241090641 | ALK | c.3387G= (p.Glu1129=) c.614G= n.264G= c.183G= (p.Glu61=) c.267G= (p.Glu89=) c.81G= (p.Glu27=) c.2256G= (p.Glu752=) c.540G= (p.Glu180=) | |
| 2 | g.29222580C>G | CA346464082 | ALK | c.3387G>C (p.Glu1129Asp) c.614G>C n.264G>C c.183G>C (p.Glu61Asp) c.267G>C (p.Glu89Asp) c.81G>C (p.Glu27Asp) c.2256G>C (p.Glu752Asp) c.540G>C (p.Glu180Asp) | |
| 2 | g.29222580C>T | CA1593965 | ALK | c.3387G>A (p.Glu1129=) c.614G>A n.264G>A c.183G>A (p.Glu61=) c.267G>A (p.Glu89=) c.81G>A (p.Glu27=) c.2256G>A (p.Glu752=) c.540G>A (p.Glu180=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 2 | g.29222581T>A | CA346464097 | ALK | c.3386A>T (p.Glu1129Val) c.613A>T n.263A>T c.182A>T (p.Glu61Val) c.266A>T (p.Glu89Val) c.80A>T (p.Glu27Val) c.2255A>T (p.Glu752Val) c.539A>T (p.Glu180Val) | dbSNP |
| 2 | g.29222581T>C | CA346464103 | ALK | c.3386A>G (p.Glu1129Gly) c.613A>G n.263A>G c.182A>G (p.Glu61Gly) c.266A>G (p.Glu89Gly) c.80A>G (p.Glu27Gly) c.2255A>G (p.Glu752Gly) c.539A>G (p.Glu180Gly) | |
| 2 | g.29222581T>G | CA346464107 | ALK | c.3386A>C (p.Glu1129Ala) c.613A>C n.263A>C c.182A>C (p.Glu61Ala) c.266A>C (p.Glu89Ala) c.80A>C (p.Glu27Ala) c.2255A>C (p.Glu752Ala) c.539A>C (p.Glu180Ala) | |
| 2 | g.29222581T= | CA1241090642 | ALK | c.3386A= (p.Glu1129=) c.613A= n.263A= c.182A= (p.Glu61=) c.266A= (p.Glu89=) c.80A= (p.Glu27=) c.2255A= (p.Glu752=) c.539A= (p.Glu180=) | |
| 2 | g.29222582C>A | CA346464110 | ALK | c.3385G>T (p.Glu1129Ter) c.612G>T n.262G>T c.181G>T (p.Glu61Ter) c.265G>T (p.Glu89Ter) c.79G>T (p.Glu27Ter) c.2254G>T (p.Glu752Ter) c.538G>T (p.Glu180Ter) | dbSNP |
| 2 | g.29222582C= | CA1241090643 | ALK | c.3385G= (p.Glu1129=) c.612G= n.262G= c.181G= (p.Glu61=) c.265G= (p.Glu89=) c.79G= (p.Glu27=) c.2254G= (p.Glu752=) c.538G= (p.Glu180=) | |
| 2 | g.29222582C>G | CA346464114 | ALK | c.3385G>C (p.Glu1129Gln) c.612G>C n.262G>C c.181G>C (p.Glu61Gln) c.265G>C (p.Glu89Gln) c.79G>C (p.Glu27Gln) c.2254G>C (p.Glu752Gln) c.538G>C (p.Glu180Gln) | dbSNP |
| 2 | g.29222582C>T | CA346464117 | ALK | c.3385G>A (p.Glu1129Lys) c.612G>A n.262G>A c.181G>A (p.Glu61Lys) c.265G>A (p.Glu89Lys) c.79G>A (p.Glu27Lys) c.2254G>A (p.Glu752Lys) c.538G>A (p.Glu180Lys) | ClinVar dbSNP COSMIC |
| 2 | g.29222585dup | CA44631364 | ALK | c.3385dup (p.Glu1129GlyfsTer4) c.612dup n.262dup c.181dup (p.Glu61GlyfsTer4) c.265dup (p.Glu89GlyfsTer4) c.79dup (p.Glu27GlyfsTer4) c.2254dup (p.Glu752GlyfsTer4) c.538dup (p.Glu180GlyfsTer4) | dbSNP |
| 2 | g.29222585del | CA645528805 | ALK | c.3385del (p.Glu1129ArgfsTer21) c.612del n.262del c.181del (p.Glu61ArgfsTer21) c.265del (p.Glu89ArgfsTer21) c.79del (p.Glu27ArgfsTer21) c.2254del (p.Glu752ArgfsTer21) c.538del (p.Glu180ArgfsTer21) | dbSNP COSMIC |
| 2 | g.29222583C>A | CA425434696 | ALK | c.3384G>T (p.Gly1128=) c.611G>T n.261G>T c.180G>T (p.Gly60=) c.264G>T (p.Gly88=) c.78G>T (p.Gly26=) c.2253G>T (p.Gly751=) c.537G>T (p.Gly179=) | dbSNP |
| 2 | g.29222583C>G | CA425434697 | ALK | c.3384G>C (p.Gly1128=) c.611G>C n.261G>C c.180G>C (p.Gly60=) c.264G>C (p.Gly88=) c.78G>C (p.Gly26=) c.2253G>C (p.Gly751=) c.537G>C (p.Gly179=) | dbSNP |
| 2 | g.29222583C>T | CA425434698 | ALK | c.3384G>A (p.Gly1128=) c.611G>A n.261G>A c.180G>A (p.Gly60=) c.264G>A (p.Gly88=) c.78G>A (p.Gly26=) c.2253G>A (p.Gly751=) c.537G>A (p.Gly179=) | dbSNP |
| 2 | g.29222584C>A | CA346464120 | ALK | c.3383G>T (p.Gly1128Val) c.610G>T n.260G>T c.179G>T (p.Gly60Val) c.263G>T (p.Gly88Val) c.77G>T (p.Gly26Val) c.2252G>T (p.Gly751Val) c.536G>T (p.Gly179Val) | |
| 2 | g.29222584C= | CA1241090644 | ALK | c.3383G= (p.Gly1128=) c.610G= n.260G= c.179G= (p.Gly60=) c.263G= (p.Gly88=) c.77G= (p.Gly26=) c.2252G= (p.Gly751=) c.536G= (p.Gly179=) | |
| 2 | g.29222584C>G | CA341484 | ALK | c.3383G>C (p.Gly1128Ala) c.610G>C n.260G>C c.179G>C (p.Gly60Ala) c.263G>C (p.Gly88Ala) c.77G>C (p.Gly26Ala) c.2252G>C (p.Gly751Ala) c.536G>C (p.Gly179Ala) | ClinVar dbSNP COSMIC |
| 2 | g.29222584C>T | CA346464122 | ALK | c.3383G>A (p.Gly1128Glu) c.610G>A n.260G>A c.179G>A (p.Gly60Glu) c.263G>A (p.Gly88Glu) c.77G>A (p.Gly26Glu) c.2252G>A (p.Gly751Glu) c.536G>A (p.Gly179Glu) | ClinVar |
| 2 | g.29222585C>A | CA346464137 | ALK | c.3382G>T (p.Gly1128Trp) c.609G>T n.259G>T c.178G>T (p.Gly60Trp) c.262G>T (p.Gly88Trp) c.76G>T (p.Gly26Trp) c.2251G>T (p.Gly751Trp) c.535G>T (p.Gly179Trp) | |
| 2 | g.29222585C= | CA1241090645 | ALK | c.3382G= (p.Gly1128=) c.609G= n.259G= c.178G= (p.Gly60=) c.262G= (p.Gly88=) c.76G= (p.Gly26=) c.2251G= (p.Gly751=) c.535G= (p.Gly179=) | |
| 2 | g.29222585C>G | CA346464142 | ALK | c.3382G>C (p.Gly1128Arg) c.609G>C n.259G>C c.178G>C (p.Gly60Arg) c.262G>C (p.Gly88Arg) c.76G>C (p.Gly26Arg) c.2251G>C (p.Gly751Arg) c.535G>C (p.Gly179Arg) | |
| 2 | g.29222585C>T | CA346464146 | ALK | c.3382G>A (p.Gly1128Arg) c.609G>A n.259G>A c.178G>A (p.Gly60Arg) c.262G>A (p.Gly88Arg) c.76G>A (p.Gly26Arg) c.2251G>A (p.Gly751Arg) c.535G>A (p.Gly179Arg) | dbSNP gnomAD v2 |
| 2 | g.29222586A>C | CA346464148 | ALK | c.3381T>G (p.Phe1127Leu) c.608T>G n.258T>G c.177T>G (p.Phe59Leu) c.261T>G (p.Phe87Leu) c.75T>G (p.Phe25Leu) c.2250T>G (p.Phe750Leu) c.534T>G (p.Phe178Leu) | dbSNP |
| 2 | g.29222586A>G | CA425434701 | ALK | c.3381T>C (p.Phe1127=) c.608T>C n.258T>C c.177T>C (p.Phe59=) c.261T>C (p.Phe87=) c.75T>C (p.Phe25=) c.2250T>C (p.Phe750=) c.534T>C (p.Phe178=) | |
| 2 | g.29222586A>T | CA346464151 | ALK | c.3381T>A (p.Phe1127Leu) c.608T>A n.258T>A c.177T>A (p.Phe59Leu) c.261T>A (p.Phe87Leu) c.75T>A (p.Phe25Leu) c.2250T>A (p.Phe750Leu) c.534T>A (p.Phe178Leu) | dbSNP |
| 2 | g.29222587A= | CA1241090646 | ALK | c.3380T= (p.Phe1127=) c.607T= n.257T= c.176T= (p.Phe59=) c.260T= (p.Phe87=) c.74T= (p.Phe25=) c.2249T= (p.Phe750=) c.533T= (p.Phe178=) | |
| 2 | g.29222587A>C | CA346464153 | ALK | c.3380T>G (p.Phe1127Cys) c.607T>G n.257T>G c.176T>G (p.Phe59Cys) c.260T>G (p.Phe87Cys) c.74T>G (p.Phe25Cys) c.2249T>G (p.Phe750Cys) c.533T>G (p.Phe178Cys) | |
| 2 | g.29222587A>G | CA346464156 | ALK | c.3380T>C (p.Phe1127Ser) c.607T>C n.257T>C c.176T>C (p.Phe59Ser) c.260T>C (p.Phe87Ser) c.74T>C (p.Phe25Ser) c.2249T>C (p.Phe750Ser) c.533T>C (p.Phe178Ser) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 2 | g.29222587A>T | CA346464160 | ALK | c.3380T>A (p.Phe1127Tyr) c.607T>A n.257T>A c.176T>A (p.Phe59Tyr) c.260T>A (p.Phe87Tyr) c.74T>A (p.Phe25Tyr) c.2249T>A (p.Phe750Tyr) c.533T>A (p.Phe178Tyr) | dbSNP |
| 2 | g.29222588A= | CA1241090647 | ALK | c.3379T= (p.Phe1127=) c.606T= n.256T= c.175T= (p.Phe59=) c.259T= (p.Phe87=) c.73T= (p.Phe25=) c.2248T= (p.Phe750=) c.532T= (p.Phe178=) | |
| 2 | g.29222588A>C | CA346464167 | ALK | c.3379T>G (p.Phe1127Val) c.606T>G n.256T>G c.175T>G (p.Phe59Val) c.259T>G (p.Phe87Val) c.73T>G (p.Phe25Val) c.2248T>G (p.Phe750Val) c.532T>G (p.Phe178Val) | dbSNP |
| 2 | g.29222588A>G | CA1593966 | ALK | c.3379T>C (p.Phe1127Leu) c.606T>C n.256T>C c.175T>C (p.Phe59Leu) c.259T>C (p.Phe87Leu) c.73T>C (p.Phe25Leu) c.2248T>C (p.Phe750Leu) c.532T>C (p.Phe178Leu) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 2 | g.29222588A>T | CA346464190 | ALK | c.3379T>A (p.Phe1127Ile) c.606T>A n.256T>A c.175T>A (p.Phe59Ile) c.259T>A (p.Phe87Ile) c.73T>A (p.Phe25Ile) c.2248T>A (p.Phe750Ile) c.532T>A (p.Phe178Ile) | dbSNP |
| 2 | g.29222589G>A | CA425434705 | ALK | c.3378C>T (p.Ala1126=) c.605C>T n.255C>T c.174C>T (p.Ala58=) c.258C>T (p.Ala86=) c.72C>T (p.Ala24=) c.2247C>T (p.Ala749=) c.531C>T (p.Ala177=) | dbSNP |
| 2 | g.29222589G>C | CA1593967 | ALK | c.3378C>G (p.Ala1126=) c.605C>G n.255C>G c.174C>G (p.Ala58=) c.258C>G (p.Ala86=) c.72C>G (p.Ala24=) c.2247C>G (p.Ala749=) c.531C>G (p.Ala177=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 2 | g.29222589G= | CA1241090648 | ALK | c.3378C= (p.Ala1126=) c.605C= n.255C= c.174C= (p.Ala58=) c.258C= (p.Ala86=) c.72C= (p.Ala24=) c.2247C= (p.Ala749=) c.531C= (p.Ala177=) | |
| 2 | g.29222589G>T | CA425434707 | ALK | c.3378C>A (p.Ala1126=) c.605C>A n.255C>A c.174C>A (p.Ala58=) c.258C>A (p.Ala86=) c.72C>A (p.Ala24=) c.2247C>A (p.Ala749=) c.531C>A (p.Ala177=) | dbSNP |
| 2 | g.29222590G>A | CA346464204 | ALK | c.3377C>T (p.Ala1126Val) c.604C>T n.254C>T c.173C>T (p.Ala58Val) c.257C>T (p.Ala86Val) c.71C>T (p.Ala24Val) c.2246C>T (p.Ala749Val) c.530C>T (p.Ala177Val) | |
| 2 | g.29222590G>C | CA346464203 | ALK | c.3377C>G (p.Ala1126Gly) c.604C>G n.254C>G c.173C>G (p.Ala58Gly) c.257C>G (p.Ala86Gly) c.71C>G (p.Ala24Gly) c.2246C>G (p.Ala749Gly) c.530C>G (p.Ala177Gly) | gnomAD v4 |
| 2 | g.29222590G>T | CA346464202 | ALK | c.3377C>A (p.Ala1126Asp) c.604C>A n.254C>A c.173C>A (p.Ala58Asp) c.257C>A (p.Ala86Asp) c.71C>A (p.Ala24Asp) c.2246C>A (p.Ala749Asp) c.530C>A (p.Ala177Asp) | ClinVar |