Primary Site >> Stomach Cancer
Gene >> CTCFL
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000243914 |
| Start | 57523681:57523681(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.525A>T |
| AA Mutation | p.Glu175Asp(p.E175D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000243914 |
| Start | 57524138:57524138(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.68C>T |
| AA Mutation | p.Pro23Leu(p.P23L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000243914 |
| Start | 57523991:57523991(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs762680387 |
| CDS Mutation | c.215C>T |
| AA Mutation | p.Ser72Leu(p.S72L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000243914 |
| Start | 57524071:57524071(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.135T>G |
| AA Mutation | p.Ser45Arg(p.S45R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000243914 |
| Start | 57523779:57523779(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.427T>C |
| AA Mutation | p.Tyr143His(p.Y143H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000243914 |
| Start | 57519231:57519231(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs753318139 |
| CDS Mutation | c.901C>T |
| AA Mutation | p.Arg301Trp(p.R301W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000243914 |
| Start | 57523955:57523955(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs144712440 |
| CDS Mutation | c.251C>T |
| AA Mutation | p.Thr84Met(p.T84M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000243914 |
| Start | 57523803:57523803(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.403G>A |
| AA Mutation | p.Ala135Thr(p.A135T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000243914 |
| Start | 57503438:57503438(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1838A>G |
| AA Mutation | p.Asp613Gly(p.D613G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000243914 |
| Start | 57503570:57503570(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1706G>A |
| AA Mutation | p.Gly569Glu(p.G569E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000243914 |
| Start | 57503449:57503449(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs146134532 |
| CDS Mutation | c.1827C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |