Primary Site >> Stomach Cancer
Gene >> APOA4
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000357780 |
| Start | 116821478:116821478(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs532465339 |
| CDS Mutation | c.580G>A |
| AA Mutation | p.Val194Met(p.V194M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000357780 |
| Start | 116821184:116821184(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.874C>A |
| AA Mutation | p.Leu292Met(p.L292M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000357780 |
| Start | 116821819:116821819(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.239T>G |
| AA Mutation | p.Leu80Arg(p.L80R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000357780 |
| Start | 116821535:116821535(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.523C>A |
| AA Mutation | p.Leu175Met(p.L175M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000357780 |
| Start | 116820956:116820956(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1102C>T |
| AA Mutation | p.Leu368Phe(p.L368F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000357780 |
| Start | 116821541:116821541(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs754506873 |
| CDS Mutation | c.517G>A |
| AA Mutation | p.Asp173Asn(p.D173N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000357780 |
| Start | 116821245:116821245(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.813C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000357780 |
| Start | 116821314:116821314(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.744C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000357780 |
| Start | 116821578:116821578(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs538954345 |
| CDS Mutation | c.480C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000357780 |
| Start | 116821668:116821668(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs771961939 |
| CDS Mutation | c.390G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000357780 |
| Start | 116821254:116821254(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.804G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000357780 |
| Start | 116821265:116821265(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs772319887 |
| CDS Mutation | c.793C>T |
| AA Mutation | p.Gln265Ter(p.Q265*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |