Primary Site >> Pancreatic Cancer
Gene >> FLG
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368799 |
| Start | 152314320:152314320(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.566A>T |
| AA Mutation | p.Glu189Val(p.E189V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368799 |
| Start | 152307592:152307592(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs775285976 |
| CDS Mutation | c.7294G>A |
| AA Mutation | p.Gly2432Arg(p.G2432R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368799 |
| Start | 152304768:152304768(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs550252644 |
| CDS Mutation | c.10118G>A |
| AA Mutation | p.Arg3373His(p.R3373H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368799 |
| Start | 152306535:152306535(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.8351A>G |
| AA Mutation | p.Asp2784Gly(p.D2784G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368799 |
| Start | 152313337:152313337(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1549C>T |
| AA Mutation | p.Arg517Cys(p.R517C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368799 |
| Start | 152305111:152305111(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs780813233 |
| CDS Mutation | c.9775G>A |
| AA Mutation | p.Glu3259Lys(p.E3259K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368799 |
| Start | 152305293:152305293(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs143183339 |
| CDS Mutation | c.9593T>G |
| AA Mutation | p.Val3198Gly(p.V3198G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368799 |
| Start | 152303166:152303166(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs554551056 |
| CDS Mutation | c.11720G>A |
| AA Mutation | p.Arg3907His(p.R3907H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368799 |
| Start | 152309702:152309702(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5184G>T |
| AA Mutation | p.Glu1728Asp(p.E1728D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000368799 |
| Start | 152310212:152310212(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4674G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000368799 |
| Start | 152303564:152303564(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs544796549 |
| CDS Mutation | c.11322C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000368799 |
| Start | 152311438:152311438(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs755996559 |
| CDS Mutation | c.3448C>T |
| AA Mutation | p.Arg1150Ter(p.R1150*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000368799 |
| Start | 152309752:152309752(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs188394023 |
| CDS Mutation | c.5134C>T |
| AA Mutation | p.Arg1712Ter(p.R1712*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | inframe_deletion |
| Transcription ID | ENST00000368799 |
| Start | 152304498:152304509(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.10377_10388delCTCAGGGTCCCA |
| AA Mutation | p.Ser3460_His3463del(p.S3460_H3463del) |
| Mutation Classification | In_Frame_Del |
| Feature Type | Transcript |