Primary Site >> Stomach Cancer
Gene >> PRKCI
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000295797 |
| Start | 170293493:170293493(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1402G>T |
| AA Mutation | p.Asp468Tyr(p.D468Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000295797 |
| Start | 170295935:170295935(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1442T>A |
| AA Mutation | p.Ile481Lys(p.I481K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000295797 |
| Start | 170267938:170267938(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs56154494 |
| CDS Mutation | c.388C>T |
| AA Mutation | p.Arg130Cys(p.R130C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000295797 |
| Start | 170280353:170280353(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.832C>T |
| AA Mutation | p.Arg278Cys(p.R278C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000295797 |
| Start | 170295931:170295931(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1438C>A |
| AA Mutation | p.Arg480Ser(p.R480S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000295797 |
| Start | 170280311:170280311(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.790A>C |
| AA Mutation | p.Ser264Arg(p.S264R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000295797 |
| Start | 170281909:170281909(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1008T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000295797 |
| Start | 170280340:170280340(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs753143066 |
| CDS Mutation | c.826delA |
| AA Mutation | p.Thr276GlnfsTer7(p.T276Qfs*7) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000295797 |
| Start | 170273305:170273311(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.614_620delAGTCATC |
| AA Mutation | p.Gln205ProfsTer10(p.Q205Pfs*10) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000295797 |
| Start | 170280376:170280377(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.861dupA |
| AA Mutation | p.Glu288ArgfsTer4(p.E288Rfs*4) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000295797 |
| Start | 170280339:170280340(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | rs756514123 |
| CDS Mutation | c.826dupA |
| AA Mutation | p.Thr276AsnfsTer16(p.T276Nfs*16) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | inframe_deletion |
| Transcription ID | ENST00000295797 |
| Start | 170280393:170280398(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.876_881delTGATGA |
| AA Mutation | p.Asp292_Asp293del(p.D292_D293del) |
| Mutation Classification | In_Frame_Del |
| Feature Type | Transcript |