Primary Site >> Stomach Cancer
Gene >> CDC25C
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000323760 |
| Start | 138325895:138325895(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.379C>G |
| AA Mutation | p.Leu127Val(p.L127V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000323760 |
| Start | 138292094:138292094(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs148887677 |
| CDS Mutation | c.638G>A |
| AA Mutation | p.Arg213His(p.R213H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000323760 |
| Start | 138329625:138329625(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs753207415 |
| CDS Mutation | c.217G>A |
| AA Mutation | p.Asp73Asn(p.D73N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000323760 |
| Start | 138287245:138287245(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.950A>C |
| AA Mutation | p.Lys317Thr(p.K317T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000323760 |
| Start | 138286120:138286120(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs776347990 |
| CDS Mutation | c.1174C>T |
| AA Mutation | p.Arg392Cys(p.R392C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000323760 |
| Start | 138325881:138325881(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs777224883 |
| CDS Mutation | c.393G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000323760 |
| Start | 138292001:138292001(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs775927964 |
| CDS Mutation | c.731delA |
| AA Mutation | p.Lys244SerfsTer15(p.K244Sfs*15) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |