Primary Site >> Pancreatic Cancer
Gene >> FASN
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000306749 |
| Start | 82091332:82091332(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1382C>T |
| AA Mutation | p.Pro461Leu(p.P461L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000306749 |
| Start | 82079518:82079518(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs765469966 |
| CDS Mutation | c.7237C>T |
| AA Mutation | p.Arg2413Cys(p.R2413C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000306749 |
| Start | 82080821:82080821(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs769486658 |
| CDS Mutation | c.6697C>T |
| AA Mutation | p.Arg2233Trp(p.R2233W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000306749 |
| Start | 82081170:82081170(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.6589G>A |
| AA Mutation | p.Ala2197Thr(p.A2197T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000306749 |
| Start | 82082027:82082027(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs774467499 |
| CDS Mutation | c.6145C>T |
| AA Mutation | p.Arg2049Trp(p.R2049W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000306749 |
| Start | 82084635:82084635(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4646C>T |
| AA Mutation | p.Ser1549Phe(p.S1549F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000306749 |
| Start | 82087227:82087227(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3250C>A |
| AA Mutation | p.Leu1084Met(p.L1084M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000306749 |
| Start | 82089383:82089383(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1967C>T |
| AA Mutation | p.Ala656Val(p.A656V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000306749 |
| Start | 82082016:82082016(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.6156C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000306749 |
| Start | 82087997:82087997(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs539431759 |
| CDS Mutation | c.2823C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |