Primary Site >> Stomach Cancer
Gene >> CKAP2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000378037 |
| Start | 52475062:52475062(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1973T>C |
| AA Mutation | p.Leu658Ser(p.L658S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000378037 |
| Start | 52468294:52468294(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs750005059 |
| CDS Mutation | c.1496G>A |
| AA Mutation | p.Arg499Gln(p.R499Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000378037 |
| Start | 52461726:52461726(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.903A>C |
| AA Mutation | p.Lys301Asn(p.K301N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000378037 |
| Start | 52474978:52474978(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs73186408 |
| CDS Mutation | c.1889G>A |
| AA Mutation | p.Arg630His(p.R630H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000378037 |
| Start | 52473900:52473900(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1621G>C |
| AA Mutation | p.Asp541His(p.D541H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000378037 |
| Start | 52461548:52461548(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.725T>C |
| AA Mutation | p.Phe242Ser(p.F242S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000378037 |
| Start | 52474899:52474899(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs752250702 |
| CDS Mutation | c.1817delA |
| AA Mutation | p.Lys606ArgfsTer14(p.K606Rfs*14) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | frameshift_variant;splice_region_variant |
| Transcription ID | ENST00000378037 |
| Start | 52461925:52461926(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.1103_1103+1insAGCTCGTCTGA |
| AA Mutation | p.Ser372LysfsTer4(p.S372Kfs*4) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | splice_donor_variant;splice_acceptor_variant;coding_sequence_variant;intron_variant |
| Transcription ID | ENST00000378037 |
| Start | 52460974:52461056(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.235_234+2delTAAGATGTGGACATAGCACTCTTAAACTGTCCCCTTTTCCATTTTGCCTTTCCTAAACACTTTTCTTAAATAATTCTTTCAGG |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |