Primary Site >> Stomach Cancer
Gene >> REC8
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000611366 |
| Start | 24178121:24178121(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs370302536 |
| CDS Mutation | c.895C>T |
| AA Mutation | p.Arg299Cys(p.R299C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000611366 |
| Start | 24177150:24177150(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.634G>A |
| AA Mutation | p.Glu212Lys(p.E212K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000611366 |
| Start | 24177192:24177192(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs559059143 |
| CDS Mutation | c.676G>A |
| AA Mutation | p.Ala226Thr(p.A226T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000611366 |
| Start | 24172749:24172749(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs779322213 |
| CDS Mutation | c.93C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000611366 |
| Start | 24173010:24173010(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.237C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000611366 |
| Start | 24172936:24172936(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.167delC |
| AA Mutation | p.Pro56ArgfsTer22(p.P56Rfs*22) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000611366 |
| Start | 24173355:24173355(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.411delT |
| AA Mutation | p.Phe137LeufsTer3(p.F137Lfs*3) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000611366 |
| Start | 24180052:24180053(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.1602_1605dupATAT |
| AA Mutation | p.Gly536IlefsTer?(p.G536Ifs*?) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |