Primary Site >> Esophagus Cancer
Gene >> ADAM12
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368679 |
| Start | 126094017:126094017(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1122G>T |
| AA Mutation | p.Glu374Asp(p.E374D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368679 |
| Start | 126019753:126019753(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2611C>G |
| AA Mutation | p.His871Asp(p.H871D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368679 |
| Start | 126064836:126064836(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs750526567 |
| CDS Mutation | c.1588G>A |
| AA Mutation | p.Glu530Lys(p.E530K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368679 |
| Start | 126019804:126019804(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2560C>G |
| AA Mutation | p.Pro854Ala(p.P854A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368679 |
| Start | 126019818:126019818(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2546G>A |
| AA Mutation | p.Cys849Tyr(p.C849Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000368679 |
| Start | 126038244:126038244(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs375026997 |
| CDS Mutation | c.2355G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000368679 |
| Start | 126046084:126046084(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1975G>T |
| AA Mutation | p.Glu659Ter(p.E659*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |