Primary Site >> Stomach Cancer
Gene >> SHISA2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000319420 |
| Start | 26046598:26046598(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.803G>A |
| AA Mutation | p.Gly268Asp(p.G268D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000319420 |
| Start | 26046647:26046647(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.754G>A |
| AA Mutation | p.Val252Met(p.V252M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000319420 |
| Start | 26047055:26047055(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs113091428 |
| CDS Mutation | c.346G>A |
| AA Mutation | p.Val116Met(p.V116M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000319420 |
| Start | 26046901:26046901(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.500T>A |
| AA Mutation | p.Ile167Asn(p.I167N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000319420 |
| Start | 26046773:26046773(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.628G>A |
| AA Mutation | p.Glu210Lys(p.E210K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000319420 |
| Start | 26046874:26046874(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs769814800 |
| CDS Mutation | c.527C>T |
| AA Mutation | p.Ser176Leu(p.S176L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |