Primary Site >> Stomach Cancer
Gene >> CTLA4
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000302823 |
| Start | 203870644:203870644(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.168T>A |
| AA Mutation | p.Phe56Leu(p.F56L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000302823 |
| Start | 203870856:203870856(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.380A>G |
| AA Mutation | p.Tyr127Cys(p.Y127C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000302823 |
| Start | 203870898:203870898(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.422T>C |
| AA Mutation | p.Leu141Pro(p.L141P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000302823 |
| Start | 203870733:203870733(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs376038796 |
| CDS Mutation | c.257C>T |
| AA Mutation | p.Ala86Val(p.A86V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000302823 |
| Start | 203870843:203870843(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.367G>A |
| AA Mutation | p.Asp123Asn(p.D123N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000302823 |
| Start | 203870748:203870748(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs1065442 |
| CDS Mutation | c.272T>C |
| AA Mutation | p.Met91Thr(p.M91T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000302823 |
| Start | 203870887:203870887(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs188862082 |
| CDS Mutation | c.411G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |