Primary Site >> Stomach Cancer
Gene >> CHAMP1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361283 |
| Start | 114325770:114325770(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs782149634 |
| CDS Mutation | c.1928C>T |
| AA Mutation | p.Ala643Val(p.A643V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361283 |
| Start | 114325134:114325134(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs547434000 |
| CDS Mutation | c.1292G>A |
| AA Mutation | p.Arg431His(p.R431H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361283 |
| Start | 114325857:114325857(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2015A>G |
| AA Mutation | p.Asp672Gly(p.D672G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361283 |
| Start | 114325833:114325833(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs782385979 |
| CDS Mutation | c.1991A>T |
| AA Mutation | p.Asp664Val(p.D664V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361283 |
| Start | 114325913:114325913(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2071G>A |
| AA Mutation | p.Ala691Thr(p.A691T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000361283 |
| Start | 114324127:114324127(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.290delA |
| AA Mutation | p.Asn97IlefsTer3(p.N97Ifs*3) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | inframe_deletion |
| Transcription ID | ENST00000361283 |
| Start | 114324393:114324395(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.553_555delCCT |
| AA Mutation | p.Pro185del(p.P185del) |
| Mutation Classification | In_Frame_Del |
| Feature Type | Transcript |