Primary Site >> Stomach Cancer
Gene >> ZBTB22
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000431845 |
| Start | 33316538:33316538(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs766099210 |
| CDS Mutation | c.379T>C |
| AA Mutation | p.Phe127Leu(p.F127L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000431845 |
| Start | 33315965:33315965(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.952G>T |
| AA Mutation | p.Asp318Tyr(p.D318Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000431845 |
| Start | 33316121:33316121(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.796G>A |
| AA Mutation | p.Asp266Asn(p.D266N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000431845 |
| Start | 33315844:33315844(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1073T>C |
| AA Mutation | p.Ile358Thr(p.I358T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000431845 |
| Start | 33316723:33316723(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.194G>A |
| AA Mutation | p.Gly65Asp(p.G65D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000431845 |
| Start | 33315564:33315564(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs760427428 |
| CDS Mutation | c.1353C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |