Primary Site >> Esophagus Cancer
Gene >> GRIN2B
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000609686 |
| Start | 13616560:13616560(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1223T>C |
| AA Mutation | p.Ile408Thr(p.I408T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000609686 |
| Start | 13866129:13866129(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200727145 |
| CDS Mutation | c.80G>A |
| AA Mutation | p.Arg27His(p.R27H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000609686 |
| Start | 13608632:13608632(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1981G>C |
| AA Mutation | p.Asp661His(p.D661H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000609686 |
| Start | 13611735:13611735(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1770T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000609686 |
| Start | 13563460:13563460(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3778C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000609686 |
| Start | 13615160:13615160(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1608C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |