Primary Site >> Stomach Cancer
Gene >> ARHGEF7
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000375741 |
| Start | 111292196:111292196(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs750569242 |
| CDS Mutation | c.2276G>A |
| AA Mutation | p.Arg759His(p.R759H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000375741 |
| Start | 111283238:111283238(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1888G>A |
| AA Mutation | p.Gly630Ser(p.G630S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000375741 |
| Start | 111280565:111280565(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs755073581 |
| CDS Mutation | c.1676C>T |
| AA Mutation | p.Ser559Leu(p.S559L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000375741 |
| Start | 111286163:111286163(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2030C>A |
| AA Mutation | p.Pro677His(p.P677H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000218789 |
| Start | 111303044:111303044(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2049C>G |
| AA Mutation | p.Asp683Glu(p.D683E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000375741 |
| Start | 111275626:111275626(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1430T>C |
| AA Mutation | p.Leu477Pro(p.L477P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000218789 |
| Start | 111300769:111300769(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1862C>T |
| AA Mutation | p.Pro621Leu(p.P621L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000375741 |
| Start | 111280657:111280657(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1768C>T |
| AA Mutation | p.His590Tyr(p.H590Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000375741 |
| Start | 111209911:111209911(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs750993031 |
| CDS Mutation | c.440C>T |
| AA Mutation | p.Ser147Leu(p.S147L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000375741 |
| Start | 111115594:111115594(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.68C>A |
| AA Mutation | p.Thr23Asn(p.T23N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000375741 |
| Start | 111283192:111283192(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200514835 |
| CDS Mutation | c.1842G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000375741 |
| Start | 111273919:111273919(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1242T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000375741 |
| Start | 111275633:111275633(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs769870955 |
| CDS Mutation | c.1437C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000375741 |
| Start | 111115587:111115587(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs754827718 |
| CDS Mutation | c.67delA |
| AA Mutation | p.Thr23ProfsTer13(p.T23Pfs*13) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |