Primary Site >> Stomach Cancer
Gene >> LPAR1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358883 |
| Start | 110941516:110941516(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs779129771 |
| CDS Mutation | c.698G>A |
| AA Mutation | p.Arg233His(p.R233H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358883 |
| Start | 110941781:110941781(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.433G>A |
| AA Mutation | p.Glu145Lys(p.E145K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358883 |
| Start | 110875437:110875437(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1079A>T |
| AA Mutation | p.Asp360Val(p.D360V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358883 |
| Start | 110941805:110941805(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.409G>A |
| AA Mutation | p.Ala137Thr(p.A137T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358883 |
| Start | 110941981:110941981(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.233G>A |
| AA Mutation | p.Arg78His(p.R78H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358883 |
| Start | 110942145:110942145(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.69G>T |
| AA Mutation | p.Gln23His(p.Q23H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000358883 |
| Start | 110875496:110875496(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1020C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000358883 |
| Start | 110875559:110875559(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs61753623 |
| CDS Mutation | c.957C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |