Primary Site >> Stomach Cancer
Gene >> ITGA1
| ID | 1 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000282588 |
| Start | 52932136:52932136(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2861G>T |
| AA Mutation | p.Ser954Ile(p.S954I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000282588 |
| Start | 52933953:52933953(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2921A>G |
| AA Mutation | p.Asn974Ser(p.N974S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000282588 |
| Start | 52861464:52861464(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200592092 |
| CDS Mutation | c.200C>T |
| AA Mutation | p.Pro67Leu(p.P67L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000282588 |
| Start | 52909005:52909005(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1563G>T |
| AA Mutation | p.Glu521Asp(p.E521D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000282588 |
| Start | 52910203:52910203(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1641G>C |
| AA Mutation | p.Gln547His(p.Q547H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000282588 |
| Start | 52932104:52932104(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs373095255 |
| CDS Mutation | c.2829G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000282588 |
| Start | 52887866:52887866(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs748796950 |
| CDS Mutation | c.825C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000282588 |
| Start | 52909026:52909026(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1584G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000282588 |
| Start | 52918846:52918846(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs764233284 |
| CDS Mutation | c.2103A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000282588 |
| Start | 52881899:52881899(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs762276627 |
| CDS Mutation | c.651C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000282588 |
| Start | 52849429:52849429(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201009495 |
| CDS Mutation | c.126G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000282588 |
| Start | 52887858:52887858(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.822delA |
| AA Mutation | p.Val275SerfsTer5(p.V275Sfs*5) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |