Primary Site >> Pancreatic Cancer
Gene >> MRC1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000569591 |
| Start | 17898139:17898139(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3356C>T |
| AA Mutation | p.Ala1119Val(p.A1119V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000569591 |
| Start | 17907684:17907684(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4064G>C |
| AA Mutation | p.Cys1355Ser(p.C1355S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000569591 |
| Start | 17861415:17861415(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1547A>G |
| AA Mutation | p.Tyr516Cys(p.Y516C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000569591 |
| Start | 17881169:17881169(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2968G>A |
| AA Mutation | p.Glu990Lys(p.E990K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000569591 |
| Start | 17910335:17910335(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4241G>T |
| AA Mutation | p.Arg1414Ile(p.R1414I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000569591 |
| Start | 17907625:17907625(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4005A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000569591 |
| Start | 17809472:17809472(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.7C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |