Primary Site >> Esophagus Cancer
Gene >> FLNC
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000325888 |
| Start | 128858149:128858149(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs760857362 |
| CDS Mutation | c.7922G>A |
| AA Mutation | p.Arg2641Gln(p.R2641Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000325888 |
| Start | 128850807:128850807(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5403G>C |
| AA Mutation | p.Glu1801Asp(p.E1801D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000325888 |
| Start | 128856844:128856844(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.7484G>C |
| AA Mutation | p.Arg2495Pro(p.R2495P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000325888 |
| Start | 128847734:128847734(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4326C>A |
| AA Mutation | p.Asp1442Glu(p.D1442E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000325888 |
| Start | 128851592:128851592(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5806C>A |
| AA Mutation | p.His1936Asn(p.H1936N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000325888 |
| Start | 128852956:128852956(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs762748670 |
| CDS Mutation | c.6133C>T |
| AA Mutation | p.Arg2045Trp(p.R2045W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000325888 |
| Start | 128830889:128830889(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.252C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000325888 |
| Start | 128846377:128846377(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4041C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |