Primary Site >> Liver Cancer
Gene >> EEA1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000322349 |
| Start | 92819405:92819405(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1631A>G |
| AA Mutation | p.Lys544Arg(p.K544R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000322349 |
| Start | 92842538:92842538(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.842A>T |
| AA Mutation | p.Gln281Leu(p.Q281L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000322349 |
| Start | 92776857:92776857(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs757264285 |
| CDS Mutation | c.4100T>C |
| AA Mutation | p.Val1367Ala(p.V1367A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000322349 |
| Start | 92811369:92811369(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2109T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000322349 |
| Start | 92811429:92811429(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs751045550 |
| CDS Mutation | c.2049A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000322349 |
| Start | 92776918:92776918(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4039A>T |
| AA Mutation | p.Arg1347Ter(p.R1347*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |