Primary Site >> Esophagus Cancer
Gene >> TNC
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000350763 |
| Start | 115062923:115062923(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs145446426 |
| CDS Mutation | c.4027G>A |
| AA Mutation | p.Val1343Ile(p.V1343I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000350763 |
| Start | 115023992:115023992(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.6476G>T |
| AA Mutation | p.Gly2159Val(p.G2159V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000350763 |
| Start | 115086182:115086182(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs765997924 |
| CDS Mutation | c.1549G>A |
| AA Mutation | p.Val517Ile(p.V517I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000350763 |
| Start | 115090895:115090895(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.124C>G |
| AA Mutation | p.Pro42Ala(p.P42A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000350763 |
| Start | 115063076:115063076(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3874G>A |
| AA Mutation | p.Glu1292Lys(p.E1292K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000350763 |
| Start | 115076041:115076041(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs139800185 |
| CDS Mutation | c.2941G>A |
| AA Mutation | p.Ala981Thr(p.A981T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000350763 |
| Start | 115087062:115087062(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs766404514 |
| CDS Mutation | c.669C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |