Primary Site >> Stomach Cancer
Gene >> ITGB2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000302347 |
| Start | 44890022:44890022(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1613C>T |
| AA Mutation | p.Thr538Ile(p.T538I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000302347 |
| Start | 44888870:44888870(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs758504990 |
| CDS Mutation | c.1903G>A |
| AA Mutation | p.Glu635Lys(p.E635K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000302347 |
| Start | 44891932:44891932(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs769736820 |
| CDS Mutation | c.1289C>T |
| AA Mutation | p.Ala430Val(p.A430V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000302347 |
| Start | 44910770:44910770(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs61737078 |
| CDS Mutation | c.13C>T |
| AA Mutation | p.Arg5Cys(p.R5C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000302347 |
| Start | 44891819:44891819(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs754683051 |
| CDS Mutation | c.1402G>A |
| AA Mutation | p.Gly468Ser(p.G468S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000302347 |
| Start | 44893491:44893491(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1137A>C |
| AA Mutation | p.Lys379Asn(p.K379N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000302347 |
| Start | 44888810:44888810(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1963A>C |
| AA Mutation | p.Asn655His(p.N655H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000302347 |
| Start | 44900409:44900409(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs148775158 |
| CDS Mutation | c.808G>A |
| AA Mutation | p.Ala270Thr(p.A270T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000302347 |
| Start | 44906990:44906990(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs548099370 |
| CDS Mutation | c.253G>A |
| AA Mutation | p.Ala85Thr(p.A85T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000302347 |
| Start | 44900388:44900388(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs752291593 |
| CDS Mutation | c.829G>A |
| AA Mutation | p.Ala277Thr(p.A277T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000302347 |
| Start | 44901704:44901704(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs373005167 |
| CDS Mutation | c.529C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000302347 |
| Start | 44889365:44889365(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs374307028 |
| CDS Mutation | c.1788C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000302347 |
| Start | 44901570:44901570(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs552709121 |
| CDS Mutation | c.663C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000302347 |
| Start | 44901501:44901501(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs146557638 |
| CDS Mutation | c.732C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000302347 |
| Start | 44900371:44900371(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs767870813 |
| CDS Mutation | c.846C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |