Primary Site >> Liver Cancer
Gene >> MCM7
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000303887 |
| Start | 100099686:100099686(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.179C>G |
| AA Mutation | p.Pro60Arg(p.P60R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000303887 |
| Start | 100097379:100097379(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1123A>G |
| AA Mutation | p.Ile375Val(p.I375V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000303887 |
| Start | 100096078:100096078(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1291G>T |
| AA Mutation | p.Gly431Cys(p.G431C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000303887 |
| Start | 100097743:100097743(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.988G>C |
| AA Mutation | p.Glu330Gln(p.E330Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000303887 |
| Start | 100095986:100095986(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1383C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000303887 |
| Start | 100094313:100094313(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1708C>T |
| AA Mutation | p.Gln570Ter(p.Q570*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | splice_acceptor_variant |
| Transcription ID | ENST00000303887 |
| Start | 100100095:100100095(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs762955038 |
| CDS Mutation | c.32-2A>G |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |