Primary Site >> Stomach Cancer
Gene >> ITGA2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000296585 |
| Start | 53048712:53048712(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.572T>A |
| AA Mutation | p.Val191Glu(p.V191E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000296585 |
| Start | 53061018:53061018(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs370400754 |
| CDS Mutation | c.1430C>T |
| AA Mutation | p.Thr477Met(p.T477M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000296585 |
| Start | 53065845:53065845(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs199827065 |
| CDS Mutation | c.1811T>C |
| AA Mutation | p.Ile604Thr(p.I604T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000296585 |
| Start | 53083388:53083388(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs370695156 |
| CDS Mutation | c.3193G>A |
| AA Mutation | p.Val1065Ile(p.V1065I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000296585 |
| Start | 53048679:53048679(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.539A>G |
| AA Mutation | p.Asp180Gly(p.D180G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000296585 |
| Start | 53058058:53058058(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1130A>G |
| AA Mutation | p.Glu377Gly(p.E377G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000296585 |
| Start | 53070226:53070226(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs148414859 |
| CDS Mutation | c.2201C>T |
| AA Mutation | p.Ala734Val(p.A734V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000296585 |
| Start | 53070239:53070239(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs142557473 |
| CDS Mutation | c.2214C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000296585 |
| Start | 53073235:53073236(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.2553dupT |
| AA Mutation | p.Ala852CysfsTer8(p.A852Cfs*8) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000296585 |
| Start | 53067164:53067165(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | rs754302389 |
| CDS Mutation | c.1996dupA |
| AA Mutation | p.Ile666AsnfsTer24(p.I666Nfs*24) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |