Primary Site >> Stomach Cancer
Gene >> IL4I1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000391826 |
| Start | 49896039:49896039(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.28G>A |
| AA Mutation | p.Val10Ile(p.V10I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000391826 |
| Start | 49894371:49894371(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs765006946 |
| CDS Mutation | c.464G>A |
| AA Mutation | p.Arg155His(p.R155H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000391826 |
| Start | 49890987:49890987(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.757C>A |
| AA Mutation | p.Leu253Ile(p.L253I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000391826 |
| Start | 49895903:49895903(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.164G>T |
| AA Mutation | p.Arg55Leu(p.R55L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000391826 |
| Start | 49895967:49895967(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs367674358 |
| CDS Mutation | c.100G>A |
| AA Mutation | p.Glu34Lys(p.E34K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000391826 |
| Start | 49894413:49894413(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.422A>G |
| AA Mutation | p.Tyr141Cys(p.Y141C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000391826 |
| Start | 49895972:49895972(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.95C>T |
| AA Mutation | p.Pro32Leu(p.P32L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000391826 |
| Start | 49894307:49894307(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.528C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000391826 |
| Start | 49889676:49889676(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1698G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000391826 |
| Start | 49890545:49890545(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.829C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000391826 |
| Start | 49889760:49889760(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1614G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000391826 |
| Start | 49894301:49894301(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs144771028 |
| CDS Mutation | c.534G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |