Primary Site >> Pancreatic Cancer
Gene >> FAT4
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394329 |
| Start | 125490707:125490707(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs748276944 |
| CDS Mutation | c.13885G>A |
| AA Mutation | p.Ala4629Thr(p.A4629T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394329 |
| Start | 125452505:125452505(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs539061913 |
| CDS Mutation | c.11489G>A |
| AA Mutation | p.Arg3830His(p.R3830H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394329 |
| Start | 125451674:125451674(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.10658C>T |
| AA Mutation | p.Pro3553Leu(p.P3553L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394329 |
| Start | 125491178:125491178(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs138173652 |
| CDS Mutation | c.14356G>A |
| AA Mutation | p.Gly4786Arg(p.G4786R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394329 |
| Start | 125317102:125317102(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.691C>T |
| AA Mutation | p.Arg231Trp(p.R231W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394329 |
| Start | 125317850:125317850(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1439A>G |
| AA Mutation | p.Tyr480Cys(p.Y480C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394329 |
| Start | 125318501:125318501(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs758608981 |
| CDS Mutation | c.2090A>G |
| AA Mutation | p.His697Arg(p.H697R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394329 |
| Start | 125319203:125319203(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2792G>T |
| AA Mutation | p.Ser931Ile(p.S931I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394329 |
| Start | 125320720:125320720(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4309A>G |
| AA Mutation | p.Thr1437Ala(p.T1437A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394329 |
| Start | 125321398:125321398(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4987G>A |
| AA Mutation | p.Val1663Met(p.V1663M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394329 |
| Start | 125450372:125450372(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.9356C>T |
| AA Mutation | p.Ala3119Val(p.A3119V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394329 |
| Start | 125491239:125491239(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.14417G>A |
| AA Mutation | p.Cys4806Tyr(p.C4806Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394329 |
| Start | 125491583:125491583(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.14761C>A |
| AA Mutation | p.Leu4921Ile(p.L4921I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000394329 |
| Start | 125319738:125319738(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs763960674 |
| CDS Mutation | c.3327C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000394329 |
| Start | 125448477:125448477(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs746567486 |
| CDS Mutation | c.7461G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000394329 |
| Start | 125320341:125320347(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.3931_3937delAATACCC |
| AA Mutation | p.Asn1311LeufsTer16(p.N1311Lfs*16) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000394329 |
| Start | 125449888:125449888(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.8872C>T |
| AA Mutation | p.Arg2958Ter(p.R2958*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |