Primary Site >> Esophagus Cancer
Gene >> LCT
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264162 |
| Start | 135822068:135822068(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.938G>A |
| AA Mutation | p.Gly313Glu(p.G313E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264162 |
| Start | 135808530:135808530(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs751898984 |
| CDS Mutation | c.3817G>A |
| AA Mutation | p.Glu1273Lys(p.E1273K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264162 |
| Start | 135804901:135804901(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs757039689 |
| CDS Mutation | c.4330G>A |
| AA Mutation | p.Val1444Met(p.V1444M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000264162 |
| Start | 135808999:135808999(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3348G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000264162 |
| Start | 135812642:135812642(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2022G>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000264162 |
| Start | 135809734:135809734(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2613T>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |