Primary Site >> Esophagus Cancer
Gene >> ZEB2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000409487 |
| Start | 144398900:144398900(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2287C>T |
| AA Mutation | p.Pro763Ser(p.P763S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000409487 |
| Start | 144389546:144389546(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3550G>C |
| AA Mutation | p.Glu1184Gln(p.E1184Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000409487 |
| Start | 144424825:144424825(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs727504227 |
| CDS Mutation | c.374C>T |
| AA Mutation | p.Thr125Met(p.T125M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000409487 |
| Start | 144400216:144400216(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.971C>T |
| AA Mutation | p.Ser324Phe(p.S324F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000409487 |
| Start | 144399146:144399146(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2041G>C |
| AA Mutation | p.Val681Leu(p.V681L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000409487 |
| Start | 144424815:144424815(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs573552493 |
| CDS Mutation | c.384C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000409487 |
| Start | 144398442:144398442(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2745C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |