Primary Site >> Stomach Cancer
Gene >> ZBTB7A
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000322357 |
| Start | 4055214:4055214(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.19G>A |
| AA Mutation | p.Gly7Ser(p.G7S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000322357 |
| Start | 4054932:4054932(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.301A>G |
| AA Mutation | p.Thr101Ala(p.T101A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000322357 |
| Start | 4048236:4048236(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1271A>C |
| AA Mutation | p.Lys424Thr(p.K424T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000322357 |
| Start | 4054899:4054899(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.334C>T |
| AA Mutation | p.Arg112Cys(p.R112C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000322357 |
| Start | 4047781:4047781(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1726G>A |
| AA Mutation | p.Asp576Asn(p.D576N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000322357 |
| Start | 4047805:4047805(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1702G>A |
| AA Mutation | p.Gly568Arg(p.G568R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000322357 |
| Start | 4047796:4047796(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs773321856 |
| CDS Mutation | c.1711C>T |
| AA Mutation | p.Pro571Ser(p.P571S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000322357 |
| Start | 4055067:4055067(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.166A>G |
| AA Mutation | p.Ser56Gly(p.S56G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | inframe_deletion |
| Transcription ID | ENST00000322357 |
| Start | 4054066:4054068(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1165_1167delAAG |
| AA Mutation | p.Lys389del(p.K389del) |
| Mutation Classification | In_Frame_Del |
| Feature Type | Transcript |