Primary Site >> Esophagus Cancer
Gene >> PROX1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261454 |
| Start | 213997470:213997470(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.935G>C |
| AA Mutation | p.Arg312Pro(p.R312P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261454 |
| Start | 213997664:213997664(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs368029419 |
| CDS Mutation | c.1129C>T |
| AA Mutation | p.Arg377Cys(p.R377C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261454 |
| Start | 213997889:213997889(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1354G>T |
| AA Mutation | p.Ala452Ser(p.A452S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261454 |
| Start | 213998208:213998208(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1673A>C |
| AA Mutation | p.Glu558Ala(p.E558A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261454 |
| Start | 213997302:213997302(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.767A>C |
| AA Mutation | p.Lys256Thr(p.K256T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261454 |
| Start | 213997919:213997919(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1384C>A |
| AA Mutation | p.Gln462Lys(p.Q462K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261454 |
| Start | 213997665:213997665(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1130G>A |
| AA Mutation | p.Arg377His(p.R377H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261454 |
| Start | 213996650:213996650(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs765586199 |
| CDS Mutation | c.115G>A |
| AA Mutation | p.Ala39Thr(p.A39T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261454 |
| Start | 213998124:213998124(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs148478012 |
| CDS Mutation | c.1589C>G |
| AA Mutation | p.Ser530Cys(p.S530C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000261454 |
| Start | 213996632:213996632(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.102delT |
| AA Mutation | p.Phe34LeufsTer12(p.F34Lfs*12) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |