Primary Site >> Esophagus Cancer
Gene >> DCLK1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360631 |
| Start | 36125813:36125813(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.325T>C |
| AA Mutation | p.Tyr109His(p.Y109H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360631 |
| Start | 35836128:35836128(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1134A>C |
| AA Mutation | p.Glu378Asp(p.E378D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000360631 |
| Start | 35808319:35808319(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1768A>C |
| AA Mutation | p.Ser590Arg(p.S590R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000360631 |
| Start | 35836134:35836134(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1128G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000360631 |
| Start | 35854544:35854544(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200783749 |
| CDS Mutation | c.990G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000360631 |
| Start | 35774664:35774664(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2094A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000360631 |
| Start | 35871283:35871284(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.880dupA |
| AA Mutation | p.Ser294LysfsTer12(p.S294Kfs*12) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |