Primary Site >> Pancreatic Cancer
Gene >> CFH
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367429 |
| Start | 196672993:196672993(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.74C>A |
| AA Mutation | p.Pro25His(p.P25H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367429 |
| Start | 196690177:196690177(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs748387954 |
| CDS Mutation | c.1274C>T |
| AA Mutation | p.Ala425Val(p.A425V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367429 |
| Start | 196715671:196715671(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1598A>T |
| AA Mutation | p.Asp533Val(p.D533V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367429 |
| Start | 196726832:196726832(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2128T>C |
| AA Mutation | p.Tyr710His(p.Y710H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000367429 |
| Start | 196745827:196745827(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3321A>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000367429 |
| Start | 196736886:196736886(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.2476delA |
| AA Mutation | p.Thr826HisfsTer2(p.T826Hfs*2) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000367429 |
| Start | 196736888:196736892(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.2479_2483delCTGAA |
| AA Mutation | p.Asn828SerfsTer37(p.N828Sfs*37) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |