Primary Site >> Stomach Cancer
Gene >> OLFM4
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000219022 |
| Start | 53041973:53041973(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.421A>G |
| AA Mutation | p.Ile141Val(p.I141V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000219022 |
| Start | 53043190:53043190(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.656T>C |
| AA Mutation | p.Leu219Pro(p.L219P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000219022 |
| Start | 53028849:53028849(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.13C>A |
| AA Mutation | p.Leu5Ile(p.L5I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000219022 |
| Start | 53050677:53050677(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs775118318 |
| CDS Mutation | c.1439G>A |
| AA Mutation | p.Ser480Asn(p.S480N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000219022 |
| Start | 53050534:53050534(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201233926 |
| CDS Mutation | c.1296C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000219022 |
| Start | 53050024:53050024(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs757133174 |
| CDS Mutation | c.786C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000219022 |
| Start | 53050138:53050138(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs750289863 |
| CDS Mutation | c.900G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000219022 |
| Start | 53028848:53028848(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs377394719 |
| CDS Mutation | c.12C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | inframe_deletion |
| Transcription ID | ENST00000219022 |
| Start | 53050073:53050075(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.835_837delTCT |
| AA Mutation | p.Ser279del(p.S279del) |
| Mutation Classification | In_Frame_Del |
| Feature Type | Transcript |