Primary Site >> Stomach Cancer
Gene >> ANXA4
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394295 |
| Start | 69806440:69806440(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.248T>A |
| AA Mutation | p.Val83Glu(p.V83E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394295 |
| Start | 69806488:69806488(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.296G>T |
| AA Mutation | p.Arg99Met(p.R99M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394295 |
| Start | 69804547:69804547(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs376382183 |
| CDS Mutation | c.112G>A |
| AA Mutation | p.Ala38Thr(p.A38T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394295 |
| Start | 69810603:69810603(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.407G>T |
| AA Mutation | p.Arg136Leu(p.R136L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000394295 |
| Start | 69812691:69812691(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs141776547 |
| CDS Mutation | c.516C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000394295 |
| Start | 69806396:69806396(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs148077345 |
| CDS Mutation | c.204C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |