Primary Site >> Esophagus Cancer
Gene >> STAB1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000321725 |
| Start | 52512855:52512855(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs748986896 |
| CDS Mutation | c.3055C>T |
| AA Mutation | p.Arg1019Cys(p.R1019C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000321725 |
| Start | 52522162:52522162(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs750412596 |
| CDS Mutation | c.6397C>T |
| AA Mutation | p.Arg2133Cys(p.R2133C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000321725 |
| Start | 52504060:52504060(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1055G>A |
| AA Mutation | p.Gly352Glu(p.G352E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000321725 |
| Start | 52516216:52516216(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4122C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000321725 |
| Start | 52516746:52516746(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs150942889 |
| CDS Mutation | c.4341C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000321725 |
| Start | 52520857:52520857(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200924394 |
| CDS Mutation | c.5760G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000321725 |
| Start | 52517949:52517949(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4707C>A |
| AA Mutation | p.Cys1569Ter(p.C1569*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | splice_donor_variant |
| Transcription ID | ENST00000321725 |
| Start | 52510237:52510237(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2628+2T>C |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | splice_acceptor_variant |
| Transcription ID | ENST00000321725 |
| Start | 52517549:52517549(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4564-1G>T |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |