Primary Site >> Stomach Cancer
Gene >> COPS5
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000357849 |
| Start | 67061963:67061963(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.34A>G |
| AA Mutation | p.Thr12Ala(p.T12A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000357849 |
| Start | 67059338:67059338(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.251A>T |
| AA Mutation | p.Lys84Met(p.K84M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000357849 |
| Start | 67043297:67043297(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.941C>A |
| AA Mutation | p.Ala314Asp(p.A314D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000357849 |
| Start | 67058171:67058171(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.419A>G |
| AA Mutation | p.His140Arg(p.H140R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000357849 |
| Start | 67057401:67057401(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs570152372 |
| CDS Mutation | c.552C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000357849 |
| Start | 67051254:67051254(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs751941822 |
| CDS Mutation | c.747G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | inframe_insertion;splice_region_variant |
| Transcription ID | ENST00000357849 |
| Start | 67045960:67045961(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.772-1_772insGTGAATACGTTGAGTTCTTCTAGCTTGCTTACT |
| AA Mutation | p.Val247_Thr257dup(p.V247_T257dup) |
| Mutation Classification | In_Frame_Ins |
| Feature Type | Transcript |