Primary Site >> Stomach Cancer
Gene >> XPR1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367590 |
| Start | 180863837:180863837(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1631A>G |
| AA Mutation | p.Asn544Ser(p.N544S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367590 |
| Start | 180880258:180880258(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1991A>G |
| AA Mutation | p.Asn664Ser(p.N664S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367590 |
| Start | 180825198:180825198(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.988A>C |
| AA Mutation | p.Ser330Arg(p.S330R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367590 |
| Start | 180806517:180806517(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.641C>A |
| AA Mutation | p.Ala214Asp(p.A214D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367590 |
| Start | 180825274:180825274(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1064T>A |
| AA Mutation | p.Met355Lys(p.M355K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367590 |
| Start | 180825297:180825297(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1087A>G |
| AA Mutation | p.Thr363Ala(p.T363A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367590 |
| Start | 180880146:180880146(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1879C>T |
| AA Mutation | p.Arg627Trp(p.R627W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367590 |
| Start | 180811421:180811421(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.696G>T |
| AA Mutation | p.Trp232Cys(p.W232C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367590 |
| Start | 180880275:180880275(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs761854990 |
| CDS Mutation | c.2008C>T |
| AA Mutation | p.Arg670Cys(p.R670C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000367590 |
| Start | 180803521:180803521(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.357T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000367590 |
| Start | 180880091:180880091(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs199985269 |
| CDS Mutation | c.1824C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |