Primary Site >> Stomach Cancer
Gene >> NELFB
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000343053 |
| Start | 137265900:137265900(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.920A>G |
| AA Mutation | p.Asp307Gly(p.D307G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000343053 |
| Start | 137256884:137256884(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs773180260 |
| CDS Mutation | c.427G>A |
| AA Mutation | p.Val143Met(p.V143M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000343053 |
| Start | 137267055:137267055(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1207T>C |
| AA Mutation | p.Tyr403His(p.Y403H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000343053 |
| Start | 137272132:137272132(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs752643955 |
| CDS Mutation | c.1397C>T |
| AA Mutation | p.Thr466Met(p.T466M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000343053 |
| Start | 137272532:137272532(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1513C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000343053 |
| Start | 137267072:137267072(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs552363247 |
| CDS Mutation | c.1224C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000343053 |
| Start | 137256928:137256928(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs182592368 |
| CDS Mutation | c.471C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |