Primary Site >> Stomach Cancer
Gene >> CAP2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000229922 |
| Start | 17551592:17551592(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1338G>T |
| AA Mutation | p.Gln446His(p.Q446H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000229922 |
| Start | 17421604:17421604(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs367682004 |
| CDS Mutation | c.49C>T |
| AA Mutation | p.Arg17Cys(p.R17C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000229922 |
| Start | 17539294:17539294(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.662C>T |
| AA Mutation | p.Ala221Val(p.A221V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000229922 |
| Start | 17507242:17507242(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.374G>A |
| AA Mutation | p.Arg125Gln(p.R125Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000229922 |
| Start | 17556364:17556364(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1356A>C |
| AA Mutation | p.Glu452Asp(p.E452D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000229922 |
| Start | 17421605:17421605(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs141863829 |
| CDS Mutation | c.50G>A |
| AA Mutation | p.Arg17His(p.R17H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |