Primary Site >> Stomach Cancer
Gene >> ZBTB2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000325144 |
| Start | 151366756:151366756(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.310G>A |
| AA Mutation | p.Ala104Thr(p.A104T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000325144 |
| Start | 151366600:151366600(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs755267853 |
| CDS Mutation | c.466G>A |
| AA Mutation | p.Gly156Arg(p.G156R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000325144 |
| Start | 151366282:151366282(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.784C>T |
| AA Mutation | p.Arg262Cys(p.R262C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000325144 |
| Start | 151366023:151366023(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1043A>G |
| AA Mutation | p.Asn348Ser(p.N348S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000325144 |
| Start | 151366513:151366513(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs768964428 |
| CDS Mutation | c.553G>A |
| AA Mutation | p.Ala185Thr(p.A185T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000325144 |
| Start | 151366285:151366285(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.781C>T |
| AA Mutation | p.Arg261Trp(p.R261W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000325144 |
| Start | 151366785:151366785(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs376506691 |
| CDS Mutation | c.281G>A |
| AA Mutation | p.Arg94Gln(p.R94Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000325144 |
| Start | 151365629:151365629(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs549133340 |
| CDS Mutation | c.1437C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |