Primary Site >> Esophagus Cancer
Gene >> EPHB1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000398015 |
| Start | 134951534:134951534(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.287G>A |
| AA Mutation | p.Cys96Tyr(p.C96Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000398015 |
| Start | 135248490:135248490(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2671G>T |
| AA Mutation | p.Val891Leu(p.V891L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000398015 |
| Start | 135192788:135192788(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2095T>G |
| AA Mutation | p.Phe699Val(p.F699V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000398015 |
| Start | 135201487:135201487(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs775383394 |
| CDS Mutation | c.2144A>G |
| AA Mutation | p.Gln715Arg(p.Q715R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000398015 |
| Start | 135162027:135162027(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1432G>C |
| AA Mutation | p.Glu478Gln(p.E478Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000398015 |
| Start | 134951391:134951391(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs371726436 |
| CDS Mutation | c.144C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000398015 |
| Start | 135259054:135259054(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2889G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000398015 |
| Start | 135179912:135179912(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs55993015 |
| CDS Mutation | c.1812C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000398015 |
| Start | 135241210:135241210(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2409A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000398015 |
| Start | 135106584:135106584(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.942T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000398015 |
| Start | 135132907:135132907(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1155C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |