Primary Site >> Stomach Cancer
Gene >> RORB
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000396204 |
| Start | 74685556:74685556(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1351A>G |
| AA Mutation | p.Thr451Ala(p.T451A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000396204 |
| Start | 74642584:74642584(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs199713370 |
| CDS Mutation | c.439G>A |
| AA Mutation | p.Glu147Lys(p.E147K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000396204 |
| Start | 74662531:74662531(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.850G>A |
| AA Mutation | p.Val284Met(p.V284M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000396204 |
| Start | 74642614:74642614(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.469G>A |
| AA Mutation | p.Val157Ile(p.V157I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000396204 |
| Start | 74634646:74634646(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.142A>C |
| AA Mutation | p.Ser48Arg(p.S48R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000396204 |
| Start | 74642572:74642572(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.427A>G |
| AA Mutation | p.Asn143Asp(p.N143D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000396204 |
| Start | 74660714:74660714(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.768A>C |
| AA Mutation | p.Glu256Asp(p.E256D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000396204 |
| Start | 74671794:74671794(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1150G>A |
| AA Mutation | p.Ala384Thr(p.A384T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000396204 |
| Start | 74685529:74685529(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1324A>G |
| AA Mutation | p.Lys442Glu(p.K442E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000396204 |
| Start | 74662518:74662518(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.837C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000396204 |
| Start | 74667795:74667795(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs764322019 |
| CDS Mutation | c.1038T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |