Primary Site >> Esophagus Cancer
Gene >> PTPN21
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000328736 |
| Start | 88485129:88485129(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1025C>A |
| AA Mutation | p.Pro342Gln(p.P342Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000328736 |
| Start | 88479345:88479345(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2086G>A |
| AA Mutation | p.Gly696Ser(p.G696S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000328736 |
| Start | 88479617:88479617(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1814C>T |
| AA Mutation | p.Thr605Met(p.T605M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000328736 |
| Start | 88480075:88480075(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1356G>C |
| AA Mutation | p.Glu452Asp(p.E452D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000328736 |
| Start | 88472258:88472258(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs112928496 |
| CDS Mutation | c.2857G>A |
| AA Mutation | p.Ala953Thr(p.A953T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000328736 |
| Start | 88479239:88479239(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2192G>A |
| AA Mutation | p.Arg731His(p.R731H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |