Primary Site >> Stomach Cancer
Gene >> GTF2B
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000370500 |
| Start | 88887344:88887344(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.41C>T |
| AA Mutation | p.Thr14Ile(p.T14I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000370500 |
| Start | 88857371:88857371(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.652T>C |
| AA Mutation | p.Phe218Leu(p.F218L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000370500 |
| Start | 88864049:88864049(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.190C>G |
| AA Mutation | p.Pro64Ala(p.P64A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000370500 |
| Start | 88860253:88860253(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.292A>G |
| AA Mutation | p.Asn98Asp(p.N98D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000370500 |
| Start | 88857421:88857421(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.602C>T |
| AA Mutation | p.Ala201Val(p.A201V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000370500 |
| Start | 88860263:88860263(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs202161057 |
| CDS Mutation | c.282C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |