Primary Site >> Esophagus Cancer
Gene >> DAPK1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358077 |
| Start | 87706412:87706412(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs375598719 |
| CDS Mutation | c.3341G>A |
| AA Mutation | p.Arg1114His(p.R1114H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358077 |
| Start | 87707150:87707150(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4079C>T |
| AA Mutation | p.Ala1360Val(p.A1360V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358077 |
| Start | 87681600:87681600(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2198C>A |
| AA Mutation | p.Pro733His(p.P733H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358077 |
| Start | 87637956:87637956(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.298G>A |
| AA Mutation | p.Glu100Lys(p.E100K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358077 |
| Start | 87707071:87707071(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4000T>G |
| AA Mutation | p.Leu1334Val(p.L1334V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000358077 |
| Start | 87697059:87697059(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2466C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000358077 |
| Start | 87706266:87706266(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3195C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000358077 |
| Start | 87706886:87706887(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | rs779681511 |
| CDS Mutation | c.3822dupG |
| AA Mutation | p.Tyr1275ValfsTer64(p.Y1275Vfs*64) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |