Primary Site >> Esophagus Cancer
Gene >> JAG2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000331782 |
| Start | 105143571:105143571(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3152C>T |
| AA Mutation | p.Ala1051Val(p.A1051V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000331782 |
| Start | 105151378:105151378(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1172C>G |
| AA Mutation | p.Ser391Trp(p.S391W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000331782 |
| Start | 105143527:105143527(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3196A>G |
| AA Mutation | p.Thr1066Ala(p.T1066A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000331782 |
| Start | 105155882:105155882(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.583C>T |
| AA Mutation | p.Arg195Cys(p.R195C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000331782 |
| Start | 105150909:105150909(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1384G>A |
| AA Mutation | p.Val462Ile(p.V462I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000331782 |
| Start | 105152180:105152180(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs138120492 |
| CDS Mutation | c.900C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |