Primary Site >> Esophagus Cancer
Gene >> FCGBP
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000616721 |
| Start | 39877783:39877783(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.9322C>G |
| AA Mutation | p.Leu3108Val(p.L3108V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000616721 |
| Start | 39894120:39894120(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5641C>G |
| AA Mutation | p.Leu1881Val(p.L1881V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000616721 |
| Start | 39894151:39894151(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5610G>T |
| AA Mutation | p.Glu1870Asp(p.E1870D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000616721 |
| Start | 39891955:39891955(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.6688G>T |
| AA Mutation | p.Ala2230Ser(p.A2230S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000616721 |
| Start | 39878062:39878062(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.9043C>T |
| AA Mutation | p.Leu3015Phe(p.L3015F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000616721 |
| Start | 39899609:39899609(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4874A>G |
| AA Mutation | p.Lys1625Arg(p.K1625R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000616721 |
| Start | 39866978:39866978(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs753812720 |
| CDS Mutation | c.12092G>A |
| AA Mutation | p.Arg4031His(p.R4031H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000616721 |
| Start | 39915292:39915292(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2722G>A |
| AA Mutation | p.Glu908Lys(p.E908K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000616721 |
| Start | 39902538:39902538(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs781896995 |
| CDS Mutation | c.4290G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000616721 |
| Start | 39892037:39892037(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.6606G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000616721 |
| Start | 39915188:39915188(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2826G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000616721 |
| Start | 39873701:39873701(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs143346927 |
| CDS Mutation | c.10698G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000616721 |
| Start | 39927915:39927915(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.447delC |
| AA Mutation | p.Gly150AlafsTer25(p.G150Afs*25) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000616721 |
| Start | 39894150:39894150(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5611C>T |
| AA Mutation | p.Gln1871Ter(p.Q1871*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |