Primary Site >> Stomach Cancer
Gene >> PKP3
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000331563 |
| Start | 404544:404544(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs754533171 |
| CDS Mutation | c.2369G>A |
| AA Mutation | p.Arg790Gln(p.R790Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000331563 |
| Start | 397114:397114(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs762556650 |
| CDS Mutation | c.613G>A |
| AA Mutation | p.Ala205Thr(p.A205T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000331563 |
| Start | 403637:403637(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs757603200 |
| CDS Mutation | c.1943G>A |
| AA Mutation | p.Arg648His(p.R648H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000331563 |
| Start | 400009:400009(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs144679997 |
| CDS Mutation | c.1316G>A |
| AA Mutation | p.Arg439His(p.R439H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000331563 |
| Start | 399100:399100(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs756559215 |
| CDS Mutation | c.1177G>A |
| AA Mutation | p.Ala393Thr(p.A393T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000331563 |
| Start | 397169:397169(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.668C>G |
| AA Mutation | p.Ser223Cys(p.S223C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000331563 |
| Start | 396663:396663(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs773017368 |
| CDS Mutation | c.288G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000331563 |
| Start | 397311:397311(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.810C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000331563 |
| Start | 400055:400055(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1366delC |
| AA Mutation | p.Leu456CysfsTer191(p.L456Cfs*191) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000331563 |
| Start | 404061:404061(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.2199delC |
| AA Mutation | p.Ile734SerfsTer66(p.I734Sfs*66) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000331563 |
| Start | 399184:399184(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1265delA |
| AA Mutation | p.Asn422MetfsTer15(p.N422Mfs*15) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000331563 |
| Start | 400071:400071(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs751960573 |
| CDS Mutation | c.1382delG |
| AA Mutation | p.Gly461ValfsTer186(p.G461Vfs*186) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000331563 |
| Start | 400076:400077(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | rs781609202 |
| CDS Mutation | c.1390dupC |
| AA Mutation | p.Leu464ProfsTer224(p.L464Pfs*224) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |