Primary Site >> Pancreatic Cancer
Gene >> MCM6
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264156 |
| Start | 135844562:135844562(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2332C>T |
| AA Mutation | p.His778Tyr(p.H778Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264156 |
| Start | 135852891:135852891(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs564036914 |
| CDS Mutation | c.1651C>T |
| AA Mutation | p.Arg551Cys(p.R551C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264156 |
| Start | 135852899:135852899(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1643T>C |
| AA Mutation | p.Ile548Thr(p.I548T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000264156 |
| Start | 135870360:135870360(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.256G>A |
| AA Mutation | p.Val86Ile(p.V86I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264156 |
| Start | 135848134:135848134(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs142938887 |
| CDS Mutation | c.1972C>T |
| AA Mutation | p.Arg658Cys(p.R658C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000264156 |
| Start | 135856764:135856764(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs372757156 |
| CDS Mutation | c.1590C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000264156 |
| Start | 135844638:135844638(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2256C>A |
| AA Mutation | p.Tyr752Ter(p.Y752*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |