Primary Site >> Stomach Cancer
Gene >> CTBP1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000290921 |
| Start | 1213534:1213534(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.965A>G |
| AA Mutation | p.Gln322Arg(p.Q322R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000290921 |
| Start | 1216179:1216179(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs776693173 |
| CDS Mutation | c.574C>T |
| AA Mutation | p.Arg192Trp(p.R192W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000290921 |
| Start | 1214383:1214383(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.853C>T |
| AA Mutation | p.Arg285Cys(p.R285C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000290921 |
| Start | 1228330:1228330(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.209C>T |
| AA Mutation | p.Ala70Val(p.A70V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000290921 |
| Start | 1213502:1213502(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.997C>T |
| AA Mutation | p.Arg333Trp(p.R333W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000290921 |
| Start | 1238201:1238201(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs772691300 |
| CDS Mutation | c.177G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000290921 |
| Start | 1214378:1214378(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs557237647 |
| CDS Mutation | c.858C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000290921 |
| Start | 1213539:1213539(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201553288 |
| CDS Mutation | c.960C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000290921 |
| Start | 1216183:1216183(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs186090455 |
| CDS Mutation | c.570G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |