Primary Site >> Stomach Cancer
Gene >> NFIB
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000380959 |
| Start | 14307198:14307198(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.353T>C |
| AA Mutation | p.Ile118Thr(p.I118T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000380959 |
| Start | 14125656:14125656(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1036G>A |
| AA Mutation | p.Gly346Arg(p.G346R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000380959 |
| Start | 14120525:14120525(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1160T>A |
| AA Mutation | p.Ile387Asn(p.I387N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000380959 |
| Start | 14120447:14120447(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1238C>T |
| AA Mutation | p.Thr413Ile(p.T413I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000380959 |
| Start | 14307162:14307162(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.389T>G |
| AA Mutation | p.Leu130Arg(p.L130R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000380959 |
| Start | 14307393:14307393(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.158A>T |
| AA Mutation | p.Glu53Val(p.E53V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000380959 |
| Start | 14120532:14120532(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1153C>T |
| AA Mutation | p.Pro385Ser(p.P385S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000380959 |
| Start | 14307365:14307365(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs770325375 |
| CDS Mutation | c.186C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000380959 |
| Start | 14307442:14307442(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.109C>T |
| AA Mutation | p.Arg37Ter(p.R37*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000380959 |
| Start | 14307409:14307409(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.142C>T |
| AA Mutation | p.Arg48Ter(p.R48*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |