Primary Site >> Liver Cancer
Gene >> FLNC
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000325888 |
| Start | 128852744:128852744(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5996G>A |
| AA Mutation | p.Arg1999Gln(p.R1999Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000325888 |
| Start | 128857130:128857130(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.7574A>T |
| AA Mutation | p.Glu2525Val(p.E2525V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000325888 |
| Start | 128844979:128844979(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3514G>A |
| AA Mutation | p.Glu1172Lys(p.E1172K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000325888 |
| Start | 128842605:128842605(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200215340 |
| CDS Mutation | c.2296C>T |
| AA Mutation | p.Arg766Trp(p.R766W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000325888 |
| Start | 128842268:128842268(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2159C>T |
| AA Mutation | p.Pro720Leu(p.P720L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000325888 |
| Start | 128846889:128846889(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs759650097 |
| CDS Mutation | c.4272G>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000325888 |
| Start | 128838031:128838031(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1014C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000325888 |
| Start | 128845158:128845158(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs765922145 |
| CDS Mutation | c.3693C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000325888 |
| Start | 128848009:128848009(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4521A>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000325888 |
| Start | 128854803:128854803(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.7026T>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000325888 |
| Start | 128849440:128849440(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5061G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000325888 |
| Start | 128830850:128830850(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.213C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000325888 |
| Start | 128854816:128854816(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs769053602 |
| CDS Mutation | c.7039C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000325888 |
| Start | 128846326:128846326(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3990T>A |
| AA Mutation | p.Tyr1330Ter(p.Y1330*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | inframe_deletion |
| Transcription ID | ENST00000325888 |
| Start | 128854452:128854460(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.6769_6777delCCATCGGGC |
| AA Mutation | p.Pro2257_Gly2259del(p.P2257_G2259del) |
| Mutation Classification | In_Frame_Del |
| Feature Type | Transcript |