Primary Site >> Stomach Cancer
Gene >> PKP2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000070846 |
| Start | 32878192:32878192(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs543281875 |
| CDS Mutation | c.688G>A |
| AA Mutation | p.Val230Ile(p.V230I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000070846 |
| Start | 32878327:32878327(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs571569344 |
| CDS Mutation | c.553C>T |
| AA Mutation | p.Arg185Trp(p.R185W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000070846 |
| Start | 32877955:32877955(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs761677945 |
| CDS Mutation | c.925G>A |
| AA Mutation | p.Ala309Thr(p.A309T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000070846 |
| Start | 32878092:32878092(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs543758984 |
| CDS Mutation | c.788C>T |
| AA Mutation | p.Thr263Met(p.T263M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000070846 |
| Start | 32821481:32821481(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs143038626 |
| CDS Mutation | c.2020G>A |
| AA Mutation | p.Val674Met(p.V674M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000070846 |
| Start | 32843273:32843273(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs377424658 |
| CDS Mutation | c.1419C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000070846 |
| Start | 32821482:32821482(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs368325383 |
| CDS Mutation | c.2019C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000070846 |
| Start | 32824144:32824144(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs780049494 |
| CDS Mutation | c.1707C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000070846 |
| Start | 32792698:32792698(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs772225819 |
| CDS Mutation | c.2523C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000070846 |
| Start | 32877980:32877980(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs140235564 |
| CDS Mutation | c.900G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000070846 |
| Start | 32796114:32796114(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs727504509 |
| CDS Mutation | c.2484C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000070846 |
| Start | 32878166:32878166(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs727503372 |
| CDS Mutation | c.714G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000070846 |
| Start | 32877905:32877905(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs369921166 |
| CDS Mutation | c.975C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | inframe_deletion |
| Transcription ID | ENST00000070846 |
| Start | 32878103:32878105(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.775_777delGAG |
| AA Mutation | p.Glu259del(p.E259del) |
| Mutation Classification | In_Frame_Del |
| Feature Type | Transcript |