Primary Site >> Stomach Cancer
Gene >> XPO5
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265351 |
| Start | 43524477:43524477(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3471C>G |
| AA Mutation | p.Cys1157Trp(p.C1157W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265351 |
| Start | 43548334:43548334(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs764867205 |
| CDS Mutation | c.1987G>A |
| AA Mutation | p.Glu663Lys(p.E663K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000265351 |
| Start | 43573601:43573601(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.106T>A |
| AA Mutation | p.Phe36Ile(p.F36I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265351 |
| Start | 43575802:43575802(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.63G>A |
| AA Mutation | p.Met21Ile(p.M21I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000265351 |
| Start | 43526710:43526710(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2958T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000265351 |
| Start | 43547677:43547677(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs774272076 |
| CDS Mutation | c.2091G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000265351 |
| Start | 43523895:43523896(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.3587dupG |
| AA Mutation | p.Gly1197TrpfsTer7(p.G1197Wfs*7) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |