Primary Site >> Esophagus Cancer
Gene >> PTPN14
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366956 |
| Start | 214384328:214384328(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1527A>C |
| AA Mutation | p.Lys509Asn(p.K509N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366956 |
| Start | 214451888:214451888(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.261C>A |
| AA Mutation | p.Asp87Glu(p.D87E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000366956 |
| Start | 214386848:214386848(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs377258229 |
| CDS Mutation | c.1062G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000366956 |
| Start | 214386893:214386893(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs138976528 |
| CDS Mutation | c.1017C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000366956 |
| Start | 214369574:214369575(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.3153dupT |
| AA Mutation | p.Ala1052CysfsTer25(p.A1052Cfs*25) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000366956 |
| Start | 214383787:214383788(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.2067_2068insT |
| AA Mutation | p.Pro690SerfsTer11(p.P690Sfs*11) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |