Primary Site >> Pancreatic Cancer
Gene >> CUL7
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265348 |
| Start | 43038366:43038366(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4674G>T |
| AA Mutation | p.Gln1558His(p.Q1558H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265348 |
| Start | 43038416:43038416(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs202082916 |
| CDS Mutation | c.4624C>T |
| AA Mutation | p.Arg1542Trp(p.R1542W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265348 |
| Start | 43048192:43048192(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2125G>A |
| AA Mutation | p.Asp709Asn(p.D709N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265348 |
| Start | 43048414:43048414(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs199607543 |
| CDS Mutation | c.1981C>T |
| AA Mutation | p.Arg661Trp(p.R661W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265348 |
| Start | 43052709:43052709(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.80G>A |
| AA Mutation | p.Arg27His(p.R27H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000265348 |
| Start | 43050398:43050398(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs747949153 |
| CDS Mutation | c.1234G>A |
| AA Mutation | p.Val412Ile(p.V412I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000265348 |
| Start | 43037886:43037886(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs762865099 |
| CDS Mutation | c.4899G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000265348 |
| Start | 43050140:43050140(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1392G>A |
| AA Mutation | p.Trp464Ter(p.W464*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |