Primary Site >> Stomach Cancer
Gene >> EEF1A2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000217182 |
| Start | 63489119:63489119(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs770611931 |
| CDS Mutation | c.1063G>A |
| AA Mutation | p.Ala355Thr(p.A355T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000217182 |
| Start | 63494972:63494972(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.454G>A |
| AA Mutation | p.Val152Met(p.V152M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000217182 |
| Start | 63488953:63488953(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1229T>C |
| AA Mutation | p.Met410Thr(p.M410T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000217182 |
| Start | 63495992:63495992(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.188T>C |
| AA Mutation | p.Leu63Pro(p.L63P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000217182 |
| Start | 63494978:63494978(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.448G>A |
| AA Mutation | p.Val150Met(p.V150M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000217182 |
| Start | 63490546:63490546(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs779441972 |
| CDS Mutation | c.962G>A |
| AA Mutation | p.Arg321Gln(p.R321Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000217182 |
| Start | 63494992:63494992(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.434T>C |
| AA Mutation | p.Val145Ala(p.V145A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000217182 |
| Start | 63495039:63495039(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs754118857 |
| CDS Mutation | c.387G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000217182 |
| Start | 63494979:63494979(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs772964838 |
| CDS Mutation | c.447C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |