Primary Site >> Stomach Cancer
Gene >> RPL22
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000234875 |
| Start | 6197668:6197668(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.101T>G |
| AA Mutation | p.Met34Arg(p.M34R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000234875 |
| Start | 6186730:6186730(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.329A>G |
| AA Mutation | p.Tyr110Cys(p.Y110C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000234875 |
| Start | 6186698:6186698(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.361G>A |
| AA Mutation | p.Glu121Lys(p.E121K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000234875 |
| Start | 6193021:6193021(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.151G>A |
| AA Mutation | p.Gly51Arg(p.G51R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000234875 |
| Start | 6186722:6186722(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs751690139 |
| CDS Mutation | c.337C>T |
| AA Mutation | p.Arg113Cys(p.R113C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000234875 |
| Start | 6186758:6186758(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 | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000234875 |
| Start | 6186681:6186681(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs376743120 |
| CDS Mutation | c.378C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000234875 |
| Start | 6197725:6197725(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs759765382 |
| CDS Mutation | c.44delA |
| AA Mutation | p.Lys15ArgfsTer5(p.K15Rfs*5) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |