Primary Site >> Stomach Cancer
Gene >> RANBP9
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000011619 |
| Start | 13634496:13634496(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1730C>T |
| AA Mutation | p.Ser577Phe(p.S577F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000011619 |
| Start | 13622417:13622417(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2135C>T |
| AA Mutation | p.Ala712Val(p.A712V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000011619 |
| Start | 13622489:13622489(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs112516735 |
| CDS Mutation | c.2063C>T |
| AA Mutation | p.Thr688Ile(p.T688I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000011619 |
| Start | 13644594:13644594(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1063C>G |
| AA Mutation | p.Arg355Gly(p.R355G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000011619 |
| Start | 13639575:13639575(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs780793088 |
| CDS Mutation | c.1513G>A |
| AA Mutation | p.Ala505Thr(p.A505T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000011619 |
| Start | 13710964:13710964(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.542C>G |
| AA Mutation | p.Ser181Cys(p.S181C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000011619 |
| Start | 13641270:13641270(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1263A>C |
| AA Mutation | p.Glu421Asp(p.E421D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000011619 |
| Start | 13637901:13637901(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1580G>A |
| AA Mutation | p.Cys527Tyr(p.C527Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000011619 |
| Start | 13644667:13644667(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.990G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000011619 |
| Start | 13634474:13634474(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs749249260 |
| CDS Mutation | c.1752C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000011619 |
| Start | 13644682:13644682(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs199849680 |
| CDS Mutation | c.975C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | inframe_deletion |
| Transcription ID | ENST00000011619 |
| Start | 13644690:13644692(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.965_967delGAG |
| AA Mutation | p.Gly322del(p.G322del) |
| Mutation Classification | In_Frame_Del |
| Feature Type | Transcript |