Primary Site >> Liver Cancer
Gene >> ATP2A2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000539276 |
| Start | 110281808:110281808(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.19A>C |
| AA Mutation | p.Lys7Gln(p.K7Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000539276 |
| Start | 110340911:110340911(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2014G>T |
| AA Mutation | p.Ala672Ser(p.A672S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000539276 |
| Start | 110327856:110327856(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.934C>T |
| AA Mutation | p.Pro312Ser(p.P312S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000539276 |
| Start | 110340968:110340968(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2071C>T |
| AA Mutation | p.Gln691Ter(p.Q691*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | inframe_deletion |
| Transcription ID | ENST00000539276 |
| Start | 110344897:110344911(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.2539_2553delACCGTGGGTGCTGCT |
| AA Mutation | p.Thr847_Ala851del(p.T847_A851del) |
| Mutation Classification | In_Frame_Del |
| Feature Type | Transcript |