Primary Site >> Liver Cancer
Gene >> MRC1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000569591 |
| Start | 17823283:17823283(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.271T>G |
| AA Mutation | p.Cys91Gly(p.C91G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000569591 |
| Start | 17885308:17885308(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3020C>A |
| AA Mutation | p.Ala1007Asp(p.A1007D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000569591 |
| Start | 17863623:17863623(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1724C>T |
| AA Mutation | p.Thr575Ile(p.T575I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000569591 |
| Start | 17909339:17909339(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4112C>T |
| AA Mutation | p.Thr1371Ile(p.T1371I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000569591 |
| Start | 17910304:17910304(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4210G>T |
| AA Mutation | p.Gly1404Cys(p.G1404C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000569591 |
| Start | 17833790:17833790(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs138394788 |
| CDS Mutation | c.753C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000569591 |
| Start | 17906977:17906977(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3891A>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000569591 |
| Start | 17823414:17823414(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.402T>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000569591 |
| Start | 17906953:17906953(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3867T>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000569591 |
| Start | 17902083:17902083(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3760A>T |
| AA Mutation | p.Arg1254Ter(p.R1254*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000569591 |
| Start | 17823416:17823416(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.404T>A |
| AA Mutation | p.Leu135Ter(p.L135*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |