Primary Site >> Stomach Cancer
Gene >> ACSL4
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000340800 |
| Start | 109659464:109659464(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1868T>C |
| AA Mutation | p.Leu623Ser(p.L623S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000340800 |
| Start | 109661580:109661580(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1771G>A |
| AA Mutation | p.Ala591Thr(p.A591T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000340800 |
| Start | 109644145:109644145(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2020A>G |
| AA Mutation | p.Ser674Gly(p.S674G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000340800 |
| Start | 109644070:109644070(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2095C>A |
| AA Mutation | p.His699Asn(p.H699N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000340800 |
| Start | 109668122:109668122(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1417G>A |
| AA Mutation | p.Gly473Ser(p.G473S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000340800 |
| Start | 109644174:109644174(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs187046661 |
| CDS Mutation | c.1991G>A |
| AA Mutation | p.Arg664Gln(p.R664Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |