Primary Site >> Stomach Cancer
Gene >> THPO
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000204615 |
| Start | 184372634:184372634(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.941C>A |
| AA Mutation | p.Pro314His(p.P314H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000204615 |
| Start | 184372583:184372583(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs372984771 |
| CDS Mutation | c.992C>T |
| AA Mutation | p.Thr331Met(p.T331M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000204615 |
| Start | 184372891:184372891(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.684G>T |
| AA Mutation | p.Lys228Asn(p.K228N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000204615 |
| Start | 184372749:184372749(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.826T>C |
| AA Mutation | p.Ser276Pro(p.S276P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000204615 |
| Start | 184375973:184375973(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.56C>T |
| AA Mutation | p.Thr19Met(p.T19M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000204615 |
| Start | 184375916:184375916(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs377412493 |
| CDS Mutation | c.113G>A |
| AA Mutation | p.Arg38His(p.R38H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000204615 |
| Start | 184373516:184373516(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.295delC |
| AA Mutation | p.Arg99GlyfsTer52(p.R99Gfs*52) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |