Primary Site >> Stomach Cancer
Gene >> IL1RL1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000233954 |
| Start | 102339005:102339005(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.230C>T |
| AA Mutation | p.Ala77Val(p.A77V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000233954 |
| Start | 102351781:102351781(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1531A>G |
| AA Mutation | p.Lys511Glu(p.K511E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000233954 |
| Start | 102340124:102340124(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs141061248 |
| CDS Mutation | c.299C>T |
| AA Mutation | p.Ala100Val(p.A100V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000233954 |
| Start | 102343366:102343366(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.921T>G |
| AA Mutation | p.Asn307Lys(p.N307K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000233954 |
| Start | 102338979:102338979(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.204A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000233954 |
| Start | 102349203:102349203(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1242C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000233954 |
| Start | 102351579:102351579(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs111942110 |
| CDS Mutation | c.1329G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | frameshift_variant;splice_region_variant |
| Transcription ID | ENST00000233954 |
| Start | 102343036:102343037(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.689dupA |
| AA Mutation | p.Asn230LysfsTer25(p.N230Kfs*25) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | splice_acceptor_variant |
| Transcription ID | ENST00000233954 |
| Start | 102338836:102338836(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.62-1G>A |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |