Primary Site >> Stomach Cancer
Gene >> NCL
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000322723 |
| Start | 231456124:231456124(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1718C>A |
| AA Mutation | p.Thr573Asn(p.T573N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000322723 |
| Start | 231460843:231460843(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.637A>T |
| AA Mutation | p.Thr213Ser(p.T213S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000322723 |
| Start | 231460276:231460276(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.916G>A |
| AA Mutation | p.Ala306Thr(p.A306T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000322723 |
| Start | 231460499:231460499(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.877G>A |
| AA Mutation | p.Ala293Thr(p.A293T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000322723 |
| Start | 231463282:231463282(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.53C>A |
| AA Mutation | p.Ala18Asp(p.A18D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000322723 |
| Start | 231461673:231461673(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.480C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000322723 |
| Start | 231460548:231460548(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.828A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000322723 |
| Start | 231461553:231461553(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs548571678 |
| CDS Mutation | c.600C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |