Primary Site >> Stomach Cancer
Gene >> EEF2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000309311 |
| Start | 3976715:3976715(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2416G>A |
| AA Mutation | p.Gly806Ser(p.G806S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000309311 |
| Start | 3979816:3979816(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1597A>G |
| AA Mutation | p.Met533Val(p.M533V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000309311 |
| Start | 3977946:3977946(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1940G>A |
| AA Mutation | p.Arg647His(p.R647H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000309311 |
| Start | 3982024:3982024(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.820A>G |
| AA Mutation | p.Ser274Gly(p.S274G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000309311 |
| Start | 3982991:3982991(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.428T>C |
| AA Mutation | p.Leu143Pro(p.L143P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000309311 |
| Start | 3980527:3980527(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1333A>C |
| AA Mutation | p.Lys445Gln(p.K445Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000309311 |
| Start | 3977577:3977577(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2101C>T |
| AA Mutation | p.Arg701Cys(p.R701C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000309311 |
| Start | 3980046:3980046(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1367G>A |
| AA Mutation | p.Arg456His(p.R456H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000309311 |
| Start | 3976717:3976717(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2414G>A |
| AA Mutation | p.Gly805Asp(p.G805D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000309311 |
| Start | 3977230:3977230(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2368G>A |
| AA Mutation | p.Val790Ile(p.V790I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000309311 |
| Start | 3978016:3978016(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs757356247 |
| CDS Mutation | c.1870G>A |
| AA Mutation | p.Ala624Thr(p.A624T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000309311 |
| Start | 3977947:3977947(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1939C>T |
| AA Mutation | p.Arg647Cys(p.R647C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000309311 |
| Start | 3979346:3979346(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs749851802 |
| CDS Mutation | c.1696G>A |
| AA Mutation | p.Ala566Thr(p.A566T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000309311 |
| Start | 3982371:3982371(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.666C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000309311 |
| Start | 3980627:3980627(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs79533804 |
| CDS Mutation | c.1233C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |