Primary Site >> Pancreatic Cancer
Gene >> FAT3
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000525166 |
| Start | 92790067:92790067(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4010G>A |
| AA Mutation | p.Arg1337Lys(p.R1337K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000525166 |
| Start | 92798211:92798211(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs150673105 |
| CDS Mutation | c.4748G>A |
| AA Mutation | p.Arg1583His(p.R1583H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000525166 |
| Start | 92867045:92867045(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs780289899 |
| CDS Mutation | c.11513C>T |
| AA Mutation | p.Ser3838Leu(p.S3838L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000525166 |
| Start | 92883300:92883300(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.12394G>A |
| AA Mutation | p.Val4132Met(p.V4132M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000525166 |
| Start | 92799377:92799377(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5914G>A |
| AA Mutation | p.Val1972Ile(p.V1972I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000525166 |
| Start | 92352648:92352648(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.86A>G |
| AA Mutation | p.Gln29Arg(p.Q29R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000525166 |
| Start | 92524912:92524912(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3121A>G |
| AA Mutation | p.Asn1041Asp(p.N1041D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000525166 |
| Start | 92798271:92798271(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4808C>A |
| AA Mutation | p.Ala1603Asp(p.A1603D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000525166 |
| Start | 92800637:92800637(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.7174G>A |
| AA Mutation | p.Asp2392Asn(p.D2392N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000525166 |
| Start | 92866811:92866811(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs376837097 |
| CDS Mutation | c.11279G>A |
| AA Mutation | p.Arg3760His(p.R3760H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000525166 |
| Start | 92843963:92843963(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.10146T>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000525166 |
| Start | 92805310:92805310(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs764868689 |
| CDS Mutation | c.8604C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |