Primary Site >> Stomach Cancer
Gene >> PRKCA
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000413366 |
| Start | 66687228:66687228(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs532000022 |
| CDS Mutation | c.647G>A |
| AA Mutation | p.Arg216His(p.R216H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000413366 |
| Start | 66645436:66645436(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs781720378 |
| CDS Mutation | c.454G>A |
| AA Mutation | p.Gly152Arg(p.G152R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000413366 |
| Start | 66302901:66302901(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.50C>A |
| AA Mutation | p.Ala17Asp(p.A17D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000413366 |
| Start | 66496281:66496281(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.286G>A |
| AA Mutation | p.Asp96Asn(p.D96N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000413366 |
| Start | 66689011:66689011(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs369357061 |
| CDS Mutation | c.882C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000413366 |
| Start | 66774037:66774037(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs770139126 |
| CDS Mutation | c.1575C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000413366 |
| Start | 66687121:66687121(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs773101122 |
| CDS Mutation | c.545delA |
| AA Mutation | p.Asn182IlefsTer2(p.N182Ifs*2) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | splice_acceptor_variant;coding_sequence_variant;intron_variant |
| Transcription ID | ENST00000413366 |
| Start | 66688946:66688969(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.822-2_843delAGGTACAAGTTGCTTAACCAAGAA |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | splice_donor_variant;coding_sequence_variant;intron_variant |
| Transcription ID | ENST00000413366 |
| Start | 66687262:66687279(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.682_686+13delACATTGTAAGTGGTCTCT |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | stop_lost |
| Transcription ID | ENST00000413366 |
| Start | 66804037:66804037(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2019A>G |
| AA Mutation | p.Ter673TrpextTer20(p.*673Wext*20) |
| Mutation Classification | Nonstop_Mutation |
| Feature Type | Transcript |