Primary Site >> Stomach Cancer
Gene >> EIF2AK2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000233057 |
| Start | 37138285:37138285(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.672T>G |
| AA Mutation | p.Ser224Arg(p.S224R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000233057 |
| Start | 37120117:37120117(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1090A>G |
| AA Mutation | p.Ile364Val(p.I364V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000233057 |
| Start | 37135509:37135509(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs758776026 |
| CDS Mutation | c.760G>A |
| AA Mutation | p.Glu254Lys(p.E254K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000233057 |
| Start | 37119993:37119993(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs765483661 |
| CDS Mutation | c.1214T>C |
| AA Mutation | p.Ile405Thr(p.I405T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000233057 |
| Start | 37126409:37126409(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.788T>C |
| AA Mutation | p.Phe263Ser(p.F263S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000233057 |
| Start | 37122658:37122658(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs771182529 |
| CDS Mutation | c.915G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000233057 |
| Start | 37136997:37136997(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.708A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000233057 |
| Start | 37107287:37107287(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs191011347 |
| CDS Mutation | c.1642C>T |
| AA Mutation | p.Arg548Ter(p.R548*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |