Primary Site >> Esophagus Cancer
Gene >> COL14A1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000297848 |
| Start | 120280740:120280740(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3676G>C |
| AA Mutation | p.Asp1226His(p.D1226H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000297848 |
| Start | 120226631:120226631(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1869A>C |
| AA Mutation | p.Glu623Asp(p.E623D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000297848 |
| Start | 120279977:120279977(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs369127166 |
| CDS Mutation | c.3524C>T |
| AA Mutation | p.Ser1175Leu(p.S1175L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000297848 |
| Start | 120280996:120280996(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3761G>C |
| AA Mutation | p.Gly1254Ala(p.G1254A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000297848 |
| Start | 120369427:120369427(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5253T>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000297848 |
| Start | 120289631:120289631(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4101T>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000297848 |
| Start | 120244001:120244001(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2472A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |