Primary Site >> Liver Cancer
Gene >> NRXN3
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000554719 |
| Start | 78803635:78803635(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.941G>A |
| AA Mutation | p.Ser314Asn(p.S314N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000557594 |
| Start | 79663785:79663785(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.437G>T |
| AA Mutation | p.Gly146Val(p.G146V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000554719 |
| Start | 78968247:78968247(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1924T>A |
| AA Mutation | p.Phe642Ile(p.F642I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000554719 |
| Start | 78968235:78968235(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1912T>A |
| AA Mutation | p.Ser638Thr(p.S638T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000557594 |
| Start | 79467226:79467226(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs373319691 |
| CDS Mutation | c.253G>A |
| AA Mutation | p.Ala85Thr(p.A85T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |