Primary Site >> Liver Cancer
Gene >> LPA
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000316300 |
| Start | 160545454:160545454(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs776342497 |
| CDS Mutation | c.5384A>G |
| AA Mutation | p.Asp1795Gly(p.D1795G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000316300 |
| Start | 160595476:160595476(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3347C>A |
| AA Mutation | p.Thr1116Asn(p.T1116N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000316300 |
| Start | 160589688:160589688(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3812T>A |
| AA Mutation | p.Val1271Asp(p.V1271D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000316300 |
| Start | 160545492:160545492(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5346C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000316300 |
| Start | 160585102:160585102(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4233T>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000316300 |
| Start | 160595430:160595430(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs758509383 |
| CDS Mutation | c.3393C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000316300 |
| Start | 160532578:160532579(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.5913dupT |
| AA Mutation | p.Lys1972Ter(p.K1972*) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |