Primary Site >> Stomach Cancer
Gene >> EIF2AK4
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263791 |
| Start | 40001111:40001111(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3046C>T |
| AA Mutation | p.His1016Tyr(p.H1016Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263791 |
| Start | 40026013:40026013(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4426C>T |
| AA Mutation | p.Arg1476Cys(p.R1476C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263791 |
| Start | 40016665:40016665(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3923A>G |
| AA Mutation | p.Lys1308Arg(p.K1308R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263791 |
| Start | 39967534:39967534(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs765950157 |
| CDS Mutation | c.1208G>A |
| AA Mutation | p.Arg403His(p.R403H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263791 |
| Start | 39973670:39973670(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1739A>G |
| AA Mutation | p.Gln580Arg(p.Q580R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263791 |
| Start | 40025989:40025989(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4402G>A |
| AA Mutation | p.Glu1468Lys(p.E1468K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263791 |
| Start | 39992178:39992178(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2635G>C |
| AA Mutation | p.Asp879His(p.D879H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263791 |
| Start | 39961861:39961861(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.821G>T |
| AA Mutation | p.Ser274Ile(p.S274I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263791 |
| Start | 40030395:40030395(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs559599794 |
| CDS Mutation | c.4598T>C |
| AA Mutation | p.Ile1533Thr(p.I1533T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000263791 |
| Start | 39965822:39965822(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.996G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000263791 |
| Start | 40008039:40008039(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3420A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000263791 |
| Start | 40017215:40017215(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs771324436 |
| CDS Mutation | c.4038C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000263791 |
| Start | 39976554:39976554(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1959C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000263791 |
| Start | 40026021:40026021(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4434G>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000263791 |
| Start | 39967853:39967853(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1527A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000263791 |
| Start | 39953958:39953958(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.574delA |
| AA Mutation | p.Arg192GlyfsTer43(p.R192Gfs*43) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000263791 |
| Start | 40034438:40034438(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.4892delA |
| AA Mutation | p.Lys1631ArgfsTer48(p.K1631Rfs*48) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000263791 |
| Start | 39990307:39990307(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.2567delT |
| AA Mutation | p.Leu856TrpfsTer7(p.L856Wfs*7) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000263791 |
| Start | 39988067:39988067(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs370269120 |
| CDS Mutation | c.2488C>T |
| AA Mutation | p.Arg830Ter(p.R830*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |