Primary Site >> Stomach Cancer
Gene >> FOXO4
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000374259 |
| Start | 71096864:71096864(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.336G>T |
| AA Mutation | p.Gln112His(p.Q112H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000374259 |
| Start | 71100853:71100853(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs766209807 |
| CDS Mutation | c.623G>A |
| AA Mutation | p.Arg208His(p.R208H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000374259 |
| Start | 71100745:71100745(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.515C>T |
| AA Mutation | p.Thr172Ile(p.T172I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000374259 |
| Start | 71101701:71101701(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs759518671 |
| CDS Mutation | c.1471A>G |
| AA Mutation | p.Met491Val(p.M491V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000374259 |
| Start | 71100969:71100969(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs749755171 |
| CDS Mutation | c.739C>T |
| AA Mutation | p.Arg247Cys(p.R247C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000374259 |
| Start | 71100805:71100805(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.575G>A |
| AA Mutation | p.Arg192His(p.R192H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000374259 |
| Start | 71101463:71101463(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs766396272 |
| CDS Mutation | c.1233C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000374259 |
| Start | 71101460:71101460(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs760792736 |
| CDS Mutation | c.1230G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000374259 |
| Start | 71096760:71096760(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.236delG |
| AA Mutation | p.Gly79AlafsTer10(p.G79Afs*10) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000374259 |
| Start | 71101427:71101427(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1203delG |
| AA Mutation | p.Leu402PhefsTer18(p.L402Ffs*18) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |