Primary Site >> Stomach Cancer
Gene >> CLU
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000316403 |
| Start | 27605107:27605107(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.646C>A |
| AA Mutation | p.Pro216Thr(p.P216T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000316403 |
| Start | 27604381:27604381(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs755878741 |
| CDS Mutation | c.844C>T |
| AA Mutation | p.Arg282Trp(p.R282W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000316403 |
| Start | 27605113:27605113(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs368909826 |
| CDS Mutation | c.640C>T |
| AA Mutation | p.Arg214Trp(p.R214W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000316403 |
| Start | 27599973:27599973(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.971G>A |
| AA Mutation | p.Arg324Gln(p.R324Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000316403 |
| Start | 27605085:27605085(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.668C>T |
| AA Mutation | p.Ser223Phe(p.S223F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000316403 |
| Start | 27605207:27605207(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs371632446 |
| CDS Mutation | c.546C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000316403 |
| Start | 27604346:27604346(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs543116935 |
| CDS Mutation | c.879G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000316403 |
| Start | 27608996:27608997(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | rs771199651 |
| CDS Mutation | c.187dupA |
| AA Mutation | p.Thr63AsnfsTer25(p.T63Nfs*25) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |