Primary Site >> Stomach Cancer
Gene >> PFKFB3
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379775 |
| Start | 6224006:6224006(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs747166742 |
| CDS Mutation | c.1262C>T |
| AA Mutation | p.Thr421Met(p.T421M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379775 |
| Start | 6213655:6213655(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200349885 |
| CDS Mutation | c.109G>A |
| AA Mutation | p.Val37Ile(p.V37I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379775 |
| Start | 6224199:6224199(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs144329353 |
| CDS Mutation | c.1327C>T |
| AA Mutation | p.Arg443Trp(p.R443W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379775 |
| Start | 6232907:6232907(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1528T>C |
| AA Mutation | p.Ser510Pro(p.S510P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379775 |
| Start | 6215313:6215313(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201889586 |
| CDS Mutation | c.295C>T |
| AA Mutation | p.Arg99Trp(p.R99W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379775 |
| Start | 6213715:6213715(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.169C>T |
| AA Mutation | p.Arg57Cys(p.R57C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000379775 |
| Start | 6219589:6219589(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.519G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000379775 |
| Start | 6221479:6221479(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs138134300 |
| CDS Mutation | c.930G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000379775 |
| Start | 6220830:6220830(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.800delG |
| AA Mutation | p.Gly267AlafsTer16(p.G267Afs*16) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |