Primary Site >> Liver Cancer
Gene >> PLEC
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000322810 |
| Start | 143930207:143930207(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2960C>A |
| AA Mutation | p.Ala987Asp(p.A987D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000322810 |
| Start | 143919511:143919511(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.10721G>A |
| AA Mutation | p.Arg3574Lys(p.R3574K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000322810 |
| Start | 143927559:143927559(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4018G>A |
| AA Mutation | p.Glu1340Lys(p.E1340K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000322810 |
| Start | 143919997:143919997(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs782481395 |
| CDS Mutation | c.10235G>A |
| AA Mutation | p.Arg3412His(p.R3412H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000322810 |
| Start | 143924163:143924163(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.6177G>C |
| AA Mutation | p.Gln2059His(p.Q2059H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000322810 |
| Start | 143917193:143917193(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs199941693 |
| CDS Mutation | c.13039G>A |
| AA Mutation | p.Ala4347Thr(p.A4347T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000322810 |
| Start | 143917430:143917430(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.12802T>G |
| AA Mutation | p.Ser4268Ala(p.S4268A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000322810 |
| Start | 143929200:143929200(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3574G>C |
| AA Mutation | p.Glu1192Gln(p.E1192Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000322810 |
| Start | 143927722:143927722(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs782313733 |
| CDS Mutation | c.3855C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |