Primary Site >> Pancreatic Cancer
Gene >> C3
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000245907 |
| Start | 6694590:6694590(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2995C>T |
| AA Mutation | p.Arg999Trp(p.R999W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000245907 |
| Start | 6684587:6684587(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4093G>T |
| AA Mutation | p.Val1365Phe(p.V1365F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000245907 |
| Start | 6694455:6694455(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3130G>A |
| AA Mutation | p.Gly1044Arg(p.G1044R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000245907 |
| Start | 6694465:6694465(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3120G>T |
| AA Mutation | p.Glu1040Asp(p.E1040D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000245907 |
| Start | 6712554:6712554(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1073C>T |
| AA Mutation | p.Thr358Ile(p.T358I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000245907 |
| Start | 6710812:6710812(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs748352684 |
| CDS Mutation | c.1513C>T |
| AA Mutation | p.Arg505Cys(p.R505C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000245907 |
| Start | 6684405:6684405(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4155C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000245907 |
| Start | 6686208:6686208(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs773963253 |
| CDS Mutation | c.3726G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000245907 |
| Start | 6696624:6696624(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2832T>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000245907 |
| Start | 6718387:6718387(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.293C>G |
| AA Mutation | p.Ser98Ter(p.S98*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |