Primary Site >> Stomach Cancer
Gene >> ITGA4
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397033 |
| Start | 181475217:181475217(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.485C>T |
| AA Mutation | p.Thr162Ile(p.T162I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000397033 |
| Start | 181494722:181494722(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1249A>G |
| AA Mutation | p.Arg417Gly(p.R417G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397033 |
| Start | 181509667:181509667(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201476802 |
| CDS Mutation | c.1705C>T |
| AA Mutation | p.Arg569Trp(p.R569W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397033 |
| Start | 181457703:181457703(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs762176587 |
| CDS Mutation | c.49C>T |
| AA Mutation | p.Arg17Trp(p.R17W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397033 |
| Start | 181457749:181457749(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.95G>A |
| AA Mutation | p.Arg32His(p.R32H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397033 |
| Start | 181474986:181474986(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.346A>G |
| AA Mutation | p.Lys116Glu(p.K116E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397033 |
| Start | 181457812:181457812(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.158G>T |
| AA Mutation | p.Gly53Val(p.G53V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397033 |
| Start | 181529544:181529544(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2434A>G |
| AA Mutation | p.Ile812Val(p.I812V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397033 |
| Start | 181478771:181478771(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs775360380 |
| CDS Mutation | c.571T>A |
| AA Mutation | p.Phe191Ile(p.F191I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397033 |
| Start | 181457776:181457776(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.122C>T |
| AA Mutation | p.Ala41Val(p.A41V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000397033 |
| Start | 181495937:181495937(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1540G>T |
| AA Mutation | p.Val514Phe(p.V514F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397033 |
| Start | 181481642:181481642(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.799G>A |
| AA Mutation | p.Glu267Lys(p.E267K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397033 |
| Start | 181493382:181493382(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1211A>G |
| AA Mutation | p.Asn404Ser(p.N404S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000397033 |
| Start | 181509699:181509699(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1737T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000397033 |
| Start | 181458301:181458301(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs772834562 |
| CDS Mutation | c.303C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000397033 |
| Start | 181534830:181534830(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs774520116 |
| CDS Mutation | c.2898A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000397033 |
| Start | 181529625:181529625(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2515C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000397033 |
| Start | 181495807:181495807(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs183217259 |
| CDS Mutation | c.1410C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000397033 |
| Start | 181458271:181458271(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.273C>A |
| AA Mutation | p.Cys91Ter(p.C91*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | splice_donor_variant |
| Transcription ID | ENST00000397033 |
| Start | 181534371:181534371(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs188628120 |
| CDS Mutation | c.2883+1G>A |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |