Primary Site >> Stomach Cancer
Gene >> ESRRB
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000380887 |
| Start | 76462577:76462577(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs376901347 |
| CDS Mutation | c.430G>A |
| AA Mutation | p.Glu144Lys(p.E144K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000380887 |
| Start | 76439655:76439655(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs755315466 |
| CDS Mutation | c.302G>A |
| AA Mutation | p.Arg101His(p.R101H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000380887 |
| Start | 76439654:76439654(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.301C>T |
| AA Mutation | p.Arg101Cys(p.R101C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000380887 |
| Start | 76439422:76439422(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs1064436 |
| CDS Mutation | c.69G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000380887 |
| Start | 76439596:76439596(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs371102435 |
| CDS Mutation | c.243C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000380887 |
| Start | 76498392:76498392(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs754937579 |
| CDS Mutation | c.1236C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000380887 |
| Start | 76498326:76498326(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1170C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000380887 |
| Start | 76462576:76462576(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs370878277 |
| CDS Mutation | c.429C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000380887 |
| Start | 76439413:76439413(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs1064434 |
| CDS Mutation | c.60G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000380887 |
| Start | 76439419:76439419(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.68delC |
| AA Mutation | p.Pro23ArgfsTer139(p.P23Rfs*139) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000380887 |
| Start | 76439536:76439555(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.184_203delTTTGCAGGCGCCGGGCTGGG |
| AA Mutation | p.Phe62ArgfsTer68(p.F62Rfs*68) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |