Primary Site >> Stomach Cancer
Gene >> XPO1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000401558 |
| Start | 61483038:61483038(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2731G>A |
| AA Mutation | p.Ala911Thr(p.A911T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000401558 |
| Start | 61495588:61495588(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.914G>A |
| AA Mutation | p.Arg305Gln(p.R305Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000401558 |
| Start | 61478851:61478851(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3185C>T |
| AA Mutation | p.Pro1062Leu(p.P1062L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000401558 |
| Start | 61492598:61492598(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1535A>G |
| AA Mutation | p.Asp512Gly(p.D512G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000401558 |
| Start | 61495582:61495582(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.920C>T |
| AA Mutation | p.Ala307Val(p.A307V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000401558 |
| Start | 61484102:61484102(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2512T>G |
| AA Mutation | p.Phe838Val(p.F838V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000401558 |
| Start | 61485959:61485959(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2317G>A |
| AA Mutation | p.Ala773Thr(p.A773T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000401558 |
| Start | 61497004:61497004(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.763C>A |
| AA Mutation | p.Leu255Met(p.L255M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000401558 |
| Start | 61485863:61485863(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2413G>A |
| AA Mutation | p.Ala805Thr(p.A805T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000401558 |
| Start | 61502286:61502286(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.326T>A |
| AA Mutation | p.Leu109His(p.L109H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000401558 |
| Start | 61493928:61493928(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1211C>A |
| AA Mutation | p.Pro404His(p.P404H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000401558 |
| Start | 61482448:61482448(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2904T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000401558 |
| Start | 61478901:61478901(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs749378477 |
| CDS Mutation | c.3135T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000401558 |
| Start | 61492338:61492338(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs150009195 |
| CDS Mutation | c.1710C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |