Primary Site >> Liver Cancer
Gene >> CDH8
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000577390 |
| Start | 61653824:61653824(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2184G>C |
| AA Mutation | p.Arg728Ser(p.R728S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000577390 |
| Start | 61655652:61655652(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1724C>A |
| AA Mutation | p.Pro575Gln(p.P575Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000577390 |
| Start | 61653646:61653646(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2362G>A |
| AA Mutation | p.Glu788Lys(p.E788K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000577390 |
| Start | 61653915:61653915(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2093A>G |
| AA Mutation | p.Lys698Arg(p.K698R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000577390 |
| Start | 61825153:61825153(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs376133486 |
| CDS Mutation | c.694A>G |
| AA Mutation | p.Met232Val(p.M232V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000577390 |
| Start | 61901309:61901309(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.417G>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |