Primary Site >> Esophagus Cancer
Gene >> ALK
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389048 |
| Start | 29532039:29532039(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1030C>T |
| AA Mutation | p.His344Tyr(p.H344Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389048 |
| Start | 29222359:29222359(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3500A>C |
| AA Mutation | p.Glu1167Ala(p.E1167A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389048 |
| Start | 29920032:29920032(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs755697363 |
| CDS Mutation | c.628G>A |
| AA Mutation | p.Ala210Thr(p.A210T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389048 |
| Start | 29228977:29228977(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2722C>A |
| AA Mutation | p.Gln908Lys(p.Q908K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389048 |
| Start | 29694961:29694961(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.841C>A |
| AA Mutation | p.His281Asn(p.H281N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389048 |
| Start | 29193760:29193760(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4327C>G |
| AA Mutation | p.Pro1443Ala(p.P1443A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389048 |
| Start | 29228967:29228967(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2732A>G |
| AA Mutation | p.Lys911Arg(p.K911R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |