Primary Site >> Stomach Cancer
Gene >> LPAR2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000407877 |
| Start | 19627043:19627043(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.242C>T |
| AA Mutation | p.Ala81Val(p.A81V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000407877 |
| Start | 19624306:19624306(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs775564995 |
| CDS Mutation | c.1006C>T |
| AA Mutation | p.Arg336Cys(p.R336C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000407877 |
| Start | 19624429:19624429(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.883T>C |
| AA Mutation | p.Tyr295His(p.Y295H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000407877 |
| Start | 19626900:19626900(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.385C>T |
| AA Mutation | p.Arg129Trp(p.R129W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000407877 |
| Start | 19624376:19624376(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs144833106 |
| CDS Mutation | c.936C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000407877 |
| Start | 19626921:19626921(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.364C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |