Primary Site >> Stomach Cancer
Gene >> PKP1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263946 |
| Start | 201283742:201283742(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.40T>C |
| AA Mutation | p.Cys14Arg(p.C14R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263946 |
| Start | 201313463:201313463(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs144063217 |
| CDS Mutation | c.604C>T |
| AA Mutation | p.Arg202Cys(p.R202C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263946 |
| Start | 201317678:201317678(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.953G>T |
| AA Mutation | p.Ser318Ile(p.S318I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263946 |
| Start | 201320292:201320292(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs146785756 |
| CDS Mutation | c.1321C>T |
| AA Mutation | p.Arg441Cys(p.R441C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263946 |
| Start | 201325060:201325060(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2017C>T |
| AA Mutation | p.Pro673Ser(p.P673S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263946 |
| Start | 201322045:201322045(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs776324521 |
| CDS Mutation | c.1478G>A |
| AA Mutation | p.Arg493His(p.R493H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263946 |
| Start | 201317629:201317629(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.904A>T |
| AA Mutation | p.Asn302Tyr(p.N302Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000263946 |
| Start | 201283902:201283902(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.200G>A |
| AA Mutation | p.Arg67Gln(p.R67Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263946 |
| Start | 201323136:201323136(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1690A>G |
| AA Mutation | p.Thr564Ala(p.T564A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263946 |
| Start | 201320334:201320334(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1363A>G |
| AA Mutation | p.Met455Val(p.M455V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000263946 |
| Start | 201313468:201313468(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs148914791 |
| CDS Mutation | c.609G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000263946 |
| Start | 201322067:201322067(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs776031745 |
| CDS Mutation | c.1500C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |