Primary Site >> Pancreatic Cancer
Gene >> FAT1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000441802 |
| Start | 186621706:186621706(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs767331775 |
| CDS Mutation | c.4880G>A |
| AA Mutation | p.Arg1627Gln(p.R1627Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000441802 |
| Start | 186588999:186588999(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs367799188 |
| CDS Mutation | c.13360G>A |
| AA Mutation | p.Glu4454Lys(p.E4454K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000441802 |
| Start | 186600143:186600143(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.11858G>T |
| AA Mutation | p.Gly3953Val(p.G3953V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000441802 |
| Start | 186617986:186617986(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.8600G>A |
| AA Mutation | p.Gly2867Asp(p.G2867D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000441802 |
| Start | 186619177:186619177(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.7409G>T |
| AA Mutation | p.Gly2470Val(p.G2470V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000441802 |
| Start | 186619253:186619253(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.7333G>T |
| AA Mutation | p.Gly2445Trp(p.G2445W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000441802 |
| Start | 186619541:186619541(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.7045G>T |
| AA Mutation | p.Asp2349Tyr(p.D2349Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000441802 |
| Start | 186706934:186706934(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2894G>A |
| AA Mutation | p.Ser965Asn(p.S965N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000441802 |
| Start | 186709256:186709256(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs758938184 |
| CDS Mutation | c.572G>A |
| AA Mutation | p.Arg191Gln(p.R191Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000441802 |
| Start | 186614285:186614285(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.9135C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000441802 |
| Start | 186603510:186603510(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.11016T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000441802 |
| Start | 186613265:186613265(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.9307G>T |
| AA Mutation | p.Gly3103Ter(p.G3103*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | splice_acceptor_variant |
| Transcription ID | ENST00000441802 |
| Start | 186617202:186617202(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.8879-1G>T |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |