Primary Site >> Esophagus Cancer
Gene >> MKI67
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368654 |
| Start | 128107858:128107858(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201476882 |
| CDS Mutation | c.3982G>A |
| AA Mutation | p.Gly1328Ser(p.G1328S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368654 |
| Start | 128105358:128105358(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.6482G>A |
| AA Mutation | p.Arg2161Lys(p.R2161K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368654 |
| Start | 128103138:128103138(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.8702G>A |
| AA Mutation | p.Ser2901Asn(p.S2901N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368654 |
| Start | 128105718:128105718(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs772060315 |
| CDS Mutation | c.6122C>T |
| AA Mutation | p.Ala2041Val(p.A2041V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368654 |
| Start | 128115156:128115156(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1252C>G |
| AA Mutation | p.Leu418Val(p.L418V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368654 |
| Start | 128103972:128103972(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs368793936 |
| CDS Mutation | c.7868C>T |
| AA Mutation | p.Thr2623Met(p.T2623M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000368654 |
| Start | 128109344:128109344(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs754452741 |
| CDS Mutation | c.2496G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000368654 |
| Start | 128112149:128112149(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs142241283 |
| CDS Mutation | c.1953G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000368654 |
| Start | 128106122:128106122(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5718G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000368654 |
| Start | 128106206:128106206(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5634G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |