Primary Site >> Stomach Cancer
Gene >> RBPJL
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000343694 |
| Start | 45312378:45312378(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.602C>T |
| AA Mutation | p.Ser201Leu(p.S201L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000343694 |
| Start | 45309607:45309607(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.172C>T |
| AA Mutation | p.Arg58Cys(p.R58C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000343694 |
| Start | 45309659:45309659(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.224A>C |
| AA Mutation | p.Lys75Thr(p.K75T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000343694 |
| Start | 45316777:45316777(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1372A>C |
| AA Mutation | p.Ser458Arg(p.S458R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000343694 |
| Start | 45314043:45314043(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.766C>T |
| AA Mutation | p.His256Tyr(p.H256Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000343694 |
| Start | 45316293:45316293(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1127C>T |
| AA Mutation | p.Ala376Val(p.A376V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000343694 |
| Start | 45312233:45312233(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.457G>A |
| AA Mutation | p.Ala153Thr(p.A153T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000343694 |
| Start | 45312226:45312226(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs751507015 |
| CDS Mutation | c.450C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |