Primary Site >> Stomach Cancer
Gene >> HSF1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000528838 |
| Start | 144312052:144312052(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs369608182 |
| CDS Mutation | c.950G>A |
| AA Mutation | p.Arg317His(p.R317H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000528838 |
| Start | 144311819:144311819(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs556226235 |
| CDS Mutation | c.843C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000528838 |
| Start | 144312086:144312086(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs782678571 |
| CDS Mutation | c.984C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000528838 |
| Start | 144311517:144311517(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.639G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000528838 |
| Start | 144314012:144314012(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1347delC |
| AA Mutation | p.Arg450GlyfsTer66(p.R450Gfs*66) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | inframe_deletion |
| Transcription ID | ENST00000528838 |
| Start | 144308962:144308976(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.177_191delGTACTTCAAGCACAA |
| AA Mutation | p.Lys59_His63del(p.K59_H63del) |
| Mutation Classification | In_Frame_Del |
| Feature Type | Transcript |