Primary Site >> Stomach Cancer
Gene >> STK33
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000315204 |
| Start | 8474839:8474839(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.67G>T |
| AA Mutation | p.Asp23Tyr(p.D23Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000315204 |
| Start | 8474857:8474857(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.49T>C |
| AA Mutation | p.Ser17Pro(p.S17P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000315204 |
| Start | 8392647:8392647(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs776825659 |
| CDS Mutation | c.1408A>G |
| AA Mutation | p.Ser470Gly(p.S470G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000315204 |
| Start | 8457371:8457371(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs537936728 |
| CDS Mutation | c.667G>A |
| AA Mutation | p.Ala223Thr(p.A223T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000315204 |
| Start | 8436076:8436076(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1011delA |
| AA Mutation | p.Gly338GlufsTer13(p.G338Efs*13) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000315204 |
| Start | 8474715:8474715(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.191delA |
| AA Mutation | p.Asn64IlefsTer6(p.N64Ifs*6) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000315204 |
| Start | 8474723:8474723(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.183delA |
| AA Mutation | p.Glu62LysfsTer8(p.E62Kfs*8) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000315204 |
| Start | 8473270:8473270(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.232A>T |
| AA Mutation | p.Arg78Ter(p.R78*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000315204 |
| Start | 8474714:8474715(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | rs757255639 |
| CDS Mutation | c.191dupA |
| AA Mutation | p.Asn64LysfsTer44(p.N64Kfs*44) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | inframe_insertion |
| Transcription ID | ENST00000315204 |
| Start | 8392538:8392539(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.1514_1516dupGCG |
| AA Mutation | p.Gly505dup(p.G505dup) |
| Mutation Classification | In_Frame_Ins |
| Feature Type | Transcript |