Primary Site >> Stomach Cancer
Gene >> HLTF
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000310053 |
| Start | 149071434:149071434(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.712A>C |
| AA Mutation | p.Thr238Pro(p.T238P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000310053 |
| Start | 149046092:149046092(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2060C>G |
| AA Mutation | p.Ala687Gly(p.A687G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000310053 |
| Start | 149046170:149046170(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1982G>A |
| AA Mutation | p.Arg661His(p.R661H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000310053 |
| Start | 149084738:149084738(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.172G>A |
| AA Mutation | p.Val58Ile(p.V58I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000310053 |
| Start | 149063440:149063440(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs773811328 |
| CDS Mutation | c.1151G>A |
| AA Mutation | p.Arg384His(p.R384H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000310053 |
| Start | 149071347:149071347(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs770061848 |
| CDS Mutation | c.799C>T |
| AA Mutation | p.Arg267Ter(p.R267*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000310053 |
| Start | 149071601:149071602(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.683dupA |
| AA Mutation | p.His228GlnfsTer2(p.H228Qfs*2) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | splice_donor_variant |
| Transcription ID | ENST00000310053 |
| Start | 149068239:149068239(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.990+1G>A |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |