Primary Site >> Stomach Cancer
Gene >> IL13RA1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371666 |
| Start | 118773935:118773935(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs775001455 |
| CDS Mutation | c.1066G>A |
| AA Mutation | p.Val356Ile(p.V356I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000371666 |
| Start | 118776509:118776509(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1189C>G |
| AA Mutation | p.Leu397Val(p.L397V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371666 |
| Start | 118761155:118761155(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.694C>T |
| AA Mutation | p.His232Tyr(p.H232Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371666 |
| Start | 118749753:118749753(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs762448978 |
| CDS Mutation | c.463G>A |
| AA Mutation | p.Asp155Asn(p.D155N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371666 |
| Start | 118791790:118791790(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1220A>G |
| AA Mutation | p.Lys407Arg(p.K407R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000371666 |
| Start | 118761277:118761277(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs754924035 |
| CDS Mutation | c.816T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |