Primary Site >> Stomach Cancer
Gene >> LPAR3
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000370611 |
| Start | 84813993:84813993(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.915G>T |
| AA Mutation | p.Lys305Asn(p.K305N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000370611 |
| Start | 84814057:84814057(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.851T>G |
| AA Mutation | p.Leu284Arg(p.L284R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000370611 |
| Start | 84866023:84866023(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.98T>G |
| AA Mutation | p.Val33Gly(p.V33G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000370611 |
| Start | 84865572:84865572(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs144051702 |
| CDS Mutation | c.549C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000370611 |
| Start | 84814155:84814155(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.753C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000370611 |
| Start | 84865455:84865455(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs140283678 |
| CDS Mutation | c.666G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |