Primary Site >> Stomach Cancer
Gene >> EIF2AK3
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000303236 |
| Start | 88557909:88557909(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3178C>A |
| AA Mutation | p.Pro1060Thr(p.P1060T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000303236 |
| Start | 88588777:88588777(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1290A>C |
| AA Mutation | p.Lys430Asn(p.K430N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000303236 |
| Start | 88585881:88585881(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1610C>T |
| AA Mutation | p.Thr537Met(p.T537M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000303236 |
| Start | 88576660:88576660(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1930G>A |
| AA Mutation | p.Ala644Thr(p.A644T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000303236 |
| Start | 88591005:88591005(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.815T>C |
| AA Mutation | p.Met272Thr(p.M272T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000303236 |
| Start | 88627055:88627055(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.220G>T |
| AA Mutation | p.Asp74Tyr(p.D74Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000303236 |
| Start | 88585950:88585950(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1541A>T |
| AA Mutation | p.Asp514Val(p.D514V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000303236 |
| Start | 88590541:88590541(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1067T>A |
| AA Mutation | p.Phe356Tyr(p.F356Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000303236 |
| Start | 88575175:88575175(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2308G>A |
| AA Mutation | p.Asp770Asn(p.D770N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000303236 |
| Start | 88590593:88590593(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs779996738 |
| CDS Mutation | c.1015A>G |
| AA Mutation | p.Ile339Val(p.I339V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000303236 |
| Start | 88585939:88585939(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1552C>G |
| AA Mutation | p.Leu518Val(p.L518V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000303236 |
| Start | 88575357:88575357(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs374554600 |
| CDS Mutation | c.2126T>C |
| AA Mutation | p.Ile709Thr(p.I709T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000303236 |
| Start | 88590586:88590586(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1022C>G |
| AA Mutation | p.Ser341Cys(p.S341C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000303236 |
| Start | 88590891:88590891(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.929T>G |
| AA Mutation | p.Ile310Arg(p.I310R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000303236 |
| Start | 88579531:88579531(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs770192517 |
| CDS Mutation | c.1873C>T |
| AA Mutation | p.Arg625Cys(p.R625C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000303236 |
| Start | 88570950:88570950(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs751166753 |
| CDS Mutation | c.2909C>T |
| AA Mutation | p.Thr970Met(p.T970M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000303236 |
| Start | 88575369:88575369(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2114C>A |
| AA Mutation | p.Thr705Lys(p.T705K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000303236 |
| Start | 88585885:88585885(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1606A>G |
| AA Mutation | p.Thr536Ala(p.T536A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000303236 |
| Start | 88588016:88588016(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1395T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000303236 |
| Start | 88590447:88590447(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1161C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000303236 |
| Start | 88575011:88575011(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2472T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000303236 |
| Start | 88590971:88590971(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.849delT |
| AA Mutation | p.Phe283LeufsTer23(p.F283Lfs*23) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000303236 |
| Start | 88579569:88579569(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1835delA |
| AA Mutation | p.Asn612ThrfsTer3(p.N612Tfs*3) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000303236 |
| Start | 88583515:88583515(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1678C>T |
| AA Mutation | p.Gln560Ter(p.Q560*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000303236 |
| Start | 88575438:88575439(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.2044dupT |
| AA Mutation | p.Trp682LeufsTer7(p.W682Lfs*7) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000303236 |
| Start | 88583447:88583448(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | rs776056726 |
| CDS Mutation | c.1745dupA |
| AA Mutation | p.Asn582LysfsTer11(p.N582Kfs*11) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 27 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000303236 |
| Start | 88588849:88588850(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.1217dupA |
| AA Mutation | p.Phe407ValfsTer13(p.F407Vfs*13) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |