Primary Site >> Stomach Cancer
Gene >> CASK
| ID | 1 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000378163 |
| Start | 41531008:41531008(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2519A>G |
| AA Mutation | p.Gln840Arg(p.Q840R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000378163 |
| Start | 41520467:41520467(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs777220099 |
| CDS Mutation | c.2734C>T |
| AA Mutation | p.Leu912Phe(p.L912F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000378163 |
| Start | 41853186:41853186(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.101C>T |
| AA Mutation | p.Thr34Ile(p.T34I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000378163 |
| Start | 41534927:41534927(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2202G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000378163 |
| Start | 41665370:41665370(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs776821824 |
| CDS Mutation | c.615C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000378163 |
| Start | 41561564:41561564(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1663delA |
| AA Mutation | p.Met555CysfsTer63(p.M555Cfs*63) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000378163 |
| Start | 41534752:41534753(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.2270dupA |
| AA Mutation | p.Asn757LysfsTer38(p.N757Kfs*38) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | splice_donor_variant;coding_sequence_variant;intron_variant |
| Transcription ID | ENST00000378163 |
| Start | 41609901:41609906(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1153_1155+3delGATGTA |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |