Primary Site >> Stomach Cancer
Gene >> FOXM1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359843 |
| Start | 2874463:2874463(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs141301985 |
| CDS Mutation | c.16C>T |
| AA Mutation | p.Arg6Cys(p.R6C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359843 |
| Start | 2859416:2859416(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs149215740 |
| CDS Mutation | c.1514C>T |
| AA Mutation | p.Ser505Leu(p.S505L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359843 |
| Start | 2858873:2858873(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2057C>T |
| AA Mutation | p.Ser686Phe(p.S686F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359843 |
| Start | 2859174:2859174(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1756T>A |
| AA Mutation | p.Ser586Thr(p.S586T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359843 |
| Start | 2868643:2868643(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs137928577 |
| CDS Mutation | c.766C>T |
| AA Mutation | p.Arg256Cys(p.R256C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359843 |
| Start | 2864405:2864405(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs552947229 |
| CDS Mutation | c.1181C>T |
| AA Mutation | p.Ser394Leu(p.S394L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359843 |
| Start | 2864492:2864492(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs759317474 |
| CDS Mutation | c.1094G>A |
| AA Mutation | p.Arg365Gln(p.R365Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359843 |
| Start | 2858954:2858954(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1976T>C |
| AA Mutation | p.Leu659Pro(p.L659P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000359843 |
| Start | 2874434:2874434(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.45G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000359843 |
| Start | 2874113:2874113(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.366G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000359843 |
| Start | 2858922:2858922(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.2008delC |
| AA Mutation | p.Glu671AsnfsTer12(p.E671Nfs*12) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000359843 |
| Start | 2859136:2859136(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1794delT |
| AA Mutation | p.Phe598LeufsTer35(p.F598Lfs*35) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000359843 |
| Start | 2858970:2858970(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs780209186 |
| CDS Mutation | c.1960delC |
| AA Mutation | p.Leu654TrpfsTer3(p.L654Wfs*3) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |