Primary Site >> Liver Cancer
Gene >> MMRN1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264790 |
| Start | 89936654:89936654(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2974G>T |
| AA Mutation | p.Gly992Cys(p.G992C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264790 |
| Start | 89935419:89935419(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1739C>A |
| AA Mutation | p.Ser580Tyr(p.S580Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264790 |
| Start | 89935194:89935194(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1514C>A |
| AA Mutation | p.Ser505Tyr(p.S505Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264790 |
| Start | 89895104:89895104(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.133C>A |
| AA Mutation | p.Pro45Thr(p.P45T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264790 |
| Start | 89895105:89895105(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.134C>A |
| AA Mutation | p.Pro45His(p.P45H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264790 |
| Start | 89895089:89895089(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs764060846 |
| CDS Mutation | c.118C>T |
| AA Mutation | p.Pro40Ser(p.P40S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000264790 |
| Start | 89935327:89935327(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1647A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000264790 |
| Start | 89935069:89935069(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1389T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000264790 |
| Start | 89936497:89936497(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2817A>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000264790 |
| Start | 89936647:89936647(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs762745325 |
| CDS Mutation | c.2967G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |