Primary Site >> Esophagus Cancer
Gene >> IGF2R
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356956 |
| Start | 160050576:160050576(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs199514599 |
| CDS Mutation | c.2618C>T |
| AA Mutation | p.Ser873Leu(p.S873L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356956 |
| Start | 160073950:160073950(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5141A>T |
| AA Mutation | p.Lys1714Ile(p.K1714I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356956 |
| Start | 160075952:160075952(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5272T>C |
| AA Mutation | p.Tyr1758His(p.Y1758H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356956 |
| Start | 160073764:160073764(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4955G>A |
| AA Mutation | p.Cys1652Tyr(p.C1652Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356956 |
| Start | 160050618:160050618(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs752875889 |
| CDS Mutation | c.2660C>T |
| AA Mutation | p.Thr887Met(p.T887M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000356956 |
| Start | 160102543:160102543(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs149900660 |
| CDS Mutation | c.6867C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000356956 |
| Start | 160080154:160080154(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5712C>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000356956 |
| Start | 160060648:160060648(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3193C>T |
| AA Mutation | p.Arg1065Ter(p.R1065*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |