Primary Site >> Stomach Cancer
Gene >> COG8
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000306875 |
| Start | 69334730:69334730(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1204G>A |
| AA Mutation | p.Ala402Thr(p.A402T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000306875 |
| Start | 69339227:69339227(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.326C>A |
| AA Mutation | p.Ala109Glu(p.A109E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000306875 |
| Start | 69334742:69334742(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1192A>C |
| AA Mutation | p.Met398Leu(p.M398L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000306875 |
| Start | 69334954:69334954(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.980T>C |
| AA Mutation | p.Leu327Pro(p.L327P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000306875 |
| Start | 69332780:69332780(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1516C>T |
| AA Mutation | p.Leu506Phe(p.L506F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000306875 |
| Start | 69339257:69339257(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.296G>A |
| AA Mutation | p.Arg99His(p.R99H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000306875 |
| Start | 69334666:69334666(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1268T>C |
| AA Mutation | p.Leu423Pro(p.L423P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000306875 |
| Start | 69335098:69335098(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.836G>A |
| AA Mutation | p.Arg279His(p.R279H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000306875 |
| Start | 69335037:69335037(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs757333246 |
| CDS Mutation | c.897G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000306875 |
| Start | 69331070:69331071(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.1607dupA |
| AA Mutation | p.Tyr537ValfsTer3(p.Y537Vfs*3) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |