Primary Site >> Stomach Cancer
Gene >> LPCAT1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000283415 |
| Start | 1501476:1501476(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs771913207 |
| CDS Mutation | c.263C>T |
| AA Mutation | p.Pro88Leu(p.P88L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000283415 |
| Start | 1463821:1463821(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1435T>C |
| AA Mutation | p.Phe479Leu(p.F479L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000283415 |
| Start | 1474606:1474606(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs138573338 |
| CDS Mutation | c.979G>A |
| AA Mutation | p.Ala327Thr(p.A327T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000283415 |
| Start | 1463722:1463722(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1534G>A |
| AA Mutation | p.Gly512Ser(p.G512S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000283415 |
| Start | 1489766:1489766(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.586T>C |
| AA Mutation | p.Ser196Pro(p.S196P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000283415 |
| Start | 1466886:1466886(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1283A>G |
| AA Mutation | p.Tyr428Cys(p.Y428C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000283415 |
| Start | 1477434:1477434(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.869A>G |
| AA Mutation | p.Tyr290Cys(p.Y290C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000283415 |
| Start | 1501569:1501569(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.170G>A |
| AA Mutation | p.Arg57Gln(p.R57Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000283415 |
| Start | 1501583:1501583(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs139981388 |
| CDS Mutation | c.156G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000283415 |
| Start | 1466885:1466885(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs372740293 |
| CDS Mutation | c.1284C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000283415 |
| Start | 1501475:1501475(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs745632669 |
| CDS Mutation | c.264G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |