Primary Site >> Liver Cancer
Gene >> PLA2G4A
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367466 |
| Start | 186911325:186911325(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.494T>A |
| AA Mutation | p.Ile165Lys(p.I165K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367466 |
| Start | 186939149:186939149(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.837A>T |
| AA Mutation | p.Leu279Phe(p.L279F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367466 |
| Start | 186911384:186911384(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs374028240 |
| CDS Mutation | c.553C>T |
| AA Mutation | p.Arg185Cys(p.R185C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367466 |
| Start | 186894140:186894140(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs28395828 |
| CDS Mutation | c.307G>A |
| AA Mutation | p.Gly103Arg(p.G103R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367466 |
| Start | 186911345:186911345(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.514C>T |
| AA Mutation | p.Leu172Phe(p.L172F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367466 |
| Start | 186979359:186979359(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2005G>T |
| AA Mutation | p.Asp669Tyr(p.D669Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000367466 |
| Start | 186870515:186870515(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.114G>A |
| AA Mutation | p.Met38Ile(p.M38I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000367466 |
| Start | 186870516:186870516(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs758024598 |
| CDS Mutation | c.115C>A |
| AA Mutation | p.Leu39Ile(p.L39I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367466 |
| Start | 186946688:186946688(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1085T>G |
| AA Mutation | p.Phe362Cys(p.F362C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000367466 |
| Start | 186979376:186979376(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2022A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000367466 |
| Start | 186911264:186911264(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs774762374 |
| CDS Mutation | c.433C>T |
| AA Mutation | p.Arg145Ter(p.R145*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |