Primary Site >> Stomach Cancer
Gene >> PRKCH
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000332981 |
| Start | 61529133:61529133(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1492T>G |
| AA Mutation | p.Phe498Val(p.F498V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000332981 |
| Start | 61549759:61549759(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1980G>T |
| AA Mutation | p.Glu660Asp(p.E660D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000332981 |
| Start | 61450969:61450969(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.830A>G |
| AA Mutation | p.Lys277Arg(p.K277R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000332981 |
| Start | 61530476:61530476(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1642C>T |
| AA Mutation | p.Leu548Phe(p.L548F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000332981 |
| Start | 61530488:61530488(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs746996721 |
| CDS Mutation | c.1654G>A |
| AA Mutation | p.Ala552Thr(p.A552T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000332981 |
| Start | 61457181:61457181(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.966C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000332981 |
| Start | 61457271:61457271(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs149356076 |
| CDS Mutation | c.1056C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000332981 |
| Start | 61530487:61530487(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs758220032 |
| CDS Mutation | c.1653C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000332981 |
| Start | 61391284:61391284(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.423T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000332981 |
| Start | 61391272:61391272(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs375154013 |
| CDS Mutation | c.411C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000332981 |
| Start | 61547793:61547793(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1812C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000332981 |
| Start | 61322314:61322315(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.217dupT |
| AA Mutation | p.Cys73LeufsTer3(p.C73Lfs*3) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |