Primary Site >> Pancreatic Cancer
Gene >> CSPG4
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000308508 |
| Start | 75685493:75685493(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs767886749 |
| CDS Mutation | c.3998C>T |
| AA Mutation | p.Ser1333Leu(p.S1333L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000308508 |
| Start | 75676631:75676631(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5888A>T |
| AA Mutation | p.Gln1963Leu(p.Q1963L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000308508 |
| Start | 75676698:75676698(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5821G>A |
| AA Mutation | p.Ala1941Thr(p.A1941T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000308508 |
| Start | 75688409:75688409(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2656C>T |
| AA Mutation | p.Leu886Phe(p.L886F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000308508 |
| Start | 75689651:75689651(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs753912977 |
| CDS Mutation | c.1414G>A |
| AA Mutation | p.Val472Met(p.V472M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000308508 |
| Start | 75690628:75690628(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.437T>C |
| AA Mutation | p.Leu146Pro(p.L146P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000308508 |
| Start | 75682949:75682949(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4542G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000308508 |
| Start | 75689226:75689226(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs567486526 |
| CDS Mutation | c.1839G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000308508 |
| Start | 75688943:75688943(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2122C>T |
| AA Mutation | p.Gln708Ter(p.Q708*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |