Primary Site >> Stomach Cancer
Gene >> LILRB4
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000391736 |
| Start | 54664381:54664381(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.551C>A |
| AA Mutation | p.Pro184His(p.P184H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000391736 |
| Start | 54666433:54666433(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.985T>G |
| AA Mutation | p.Phe329Val(p.F329V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000391736 |
| Start | 54666433:54666433(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.985T>C |
| AA Mutation | p.Phe329Leu(p.F329L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000391736 |
| Start | 54666298:54666298(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs372467569 |
| CDS Mutation | c.933C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000391736 |
| Start | 54667743:54667743(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1150C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000391736 |
| Start | 54663039:54663039(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.6C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000391736 |
| Start | 54663809:54663809(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs775831330 |
| CDS Mutation | c.126G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |