Primary Site >> Pancreatic Cancer
Gene >> FN1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359671 |
| Start | 215382260:215382260(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4843C>G |
| AA Mutation | p.Gln1615Glu(p.Q1615E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000359671 |
| Start | 215424148:215424148(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1214C>T |
| AA Mutation | p.Thr405Ile(p.T405I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359671 |
| Start | 215375303:215375303(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5795G>A |
| AA Mutation | p.Gly1932Asp(p.G1932D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359671 |
| Start | 215407133:215407133(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2707C>T |
| AA Mutation | p.Arg903Cys(p.R903C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359671 |
| Start | 215410056:215410056(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2000C>T |
| AA Mutation | p.Thr667Ile(p.T667I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359671 |
| Start | 215423496:215423496(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs181283286 |
| CDS Mutation | c.1247A>G |
| AA Mutation | p.Asn416Ser(p.N416S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000359671 |
| Start | 215384870:215384870(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs147150819 |
| CDS Mutation | c.4446C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000359671 |
| Start | 215386723:215386723(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs754043219 |
| CDS Mutation | c.4305G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000359671 |
| Start | 215428228:215428228(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.796G>T |
| AA Mutation | p.Gly266Ter(p.G266*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |