Primary Site >> Stomach Cancer
Gene >> LTA
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000454783 |
| Start | 31573325:31573325(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.250G>A |
| AA Mutation | p.Asp84Asn(p.D84N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000454783 |
| Start | 31573302:31573302(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs780069099 |
| CDS Mutation | c.227C>T |
| AA Mutation | p.Ser76Leu(p.S76L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000454783 |
| Start | 31572974:31572974(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs368539892 |
| CDS Mutation | c.146G>A |
| AA Mutation | p.Arg49His(p.R49H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000454783 |
| Start | 31573301:31573301(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.226T>C |
| AA Mutation | p.Ser76Pro(p.S76P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000454783 |
| Start | 31573688:31573688(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.613C>A |
| AA Mutation | p.Leu205Met(p.L205M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000454783 |
| Start | 31573573:31573573(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs766877367 |
| CDS Mutation | c.498G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |