Primary Site >> Stomach Cancer
Gene >> CTBP2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000337195 |
| Start | 125003486:125003486(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs755005723 |
| CDS Mutation | c.65G>A |
| AA Mutation | p.Arg22His(p.R22H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000337195 |
| Start | 124994614:124994614(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.635A>G |
| AA Mutation | p.Tyr212Cys(p.Y212C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000337195 |
| Start | 124994525:124994525(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.724C>T |
| AA Mutation | p.His242Tyr(p.H242Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000337195 |
| Start | 125003002:125003002(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.316A>C |
| AA Mutation | p.Ser106Arg(p.S106R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000337195 |
| Start | 125003083:125003083(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.235G>A |
| AA Mutation | p.Ala79Thr(p.A79T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000337195 |
| Start | 125003103:125003103(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.215T>C |
| AA Mutation | p.Val72Ala(p.V72A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000337195 |
| Start | 124994585:124994585(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.664G>T |
| AA Mutation | p.Gly222Cys(p.G222C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000337195 |
| Start | 124993935:124993935(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs148275243 |
| CDS Mutation | c.831C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000337195 |
| Start | 125003344:125003344(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.207C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000337195 |
| Start | 125003015:125003015(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs145557678 |
| CDS Mutation | c.303C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000337195 |
| Start | 125003425:125003425(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs202167377 |
| CDS Mutation | c.126C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |