Primary Site >> Stomach Cancer
Gene >> HSF4
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264009 |
| Start | 67167523:67167523(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs781742797 |
| CDS Mutation | c.778C>T |
| AA Mutation | p.Pro260Ser(p.P260S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264009 |
| Start | 67166589:67166589(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs374589300 |
| CDS Mutation | c.593C>T |
| AA Mutation | p.Ala198Val(p.A198V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264009 |
| Start | 67165817:67165817(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.331G>A |
| AA Mutation | p.Glu111Lys(p.E111K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264009 |
| Start | 67165821:67165821(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.335A>G |
| AA Mutation | p.Gln112Arg(p.Q112R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264009 |
| Start | 67165833:67165833(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs79121622 |
| CDS Mutation | c.347G>A |
| AA Mutation | p.Arg116His(p.R116H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264009 |
| Start | 67165616:67165616(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.218G>A |
| AA Mutation | p.Arg73His(p.R73H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264009 |
| Start | 67165745:67165745(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs367654370 |
| CDS Mutation | c.259G>A |
| AA Mutation | p.Glu87Lys(p.E87K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264009 |
| Start | 67166340:67166340(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.506G>A |
| AA Mutation | p.Arg169Gln(p.R169Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000264009 |
| Start | 67167763:67167763(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs760309963 |
| CDS Mutation | c.904delG |
| AA Mutation | p.Asp302MetfsTer17(p.D302Mfs*17) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |