Primary Site >> Stomach Cancer
Gene >> CD5
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000347785 |
| Start | 61121653:61121653(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.848G>A |
| AA Mutation | p.Ser283Asn(p.S283N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000347785 |
| Start | 61121679:61121679(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs759626085 |
| CDS Mutation | c.874C>T |
| AA Mutation | p.Arg292Cys(p.R292C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000347785 |
| Start | 61118312:61118312(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.232T>C |
| AA Mutation | p.Ser78Pro(p.S78P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000347785 |
| Start | 61118404:61118404(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs758833606 |
| CDS Mutation | c.324C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000347785 |
| Start | 61125093:61125093(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1341C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000347785 |
| Start | 61118952:61118952(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs753011554 |
| CDS Mutation | c.438G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |