Primary Site >> Stomach Cancer
Gene >> ITGA3
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000320031 |
| Start | 50071417:50071417(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.858G>T |
| AA Mutation | p.Gln286His(p.Q286H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000320031 |
| Start | 50077382:50077382(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2074G>A |
| AA Mutation | p.Gly692Arg(p.G692R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000320031 |
| Start | 50080329:50080329(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2774C>T |
| AA Mutation | p.Thr925Ile(p.T925I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000320031 |
| Start | 50074261:50074261(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1363G>T |
| AA Mutation | p.Asp455Tyr(p.D455Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000320031 |
| Start | 50068222:50068222(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs766240466 |
| CDS Mutation | c.581C>T |
| AA Mutation | p.Thr194Met(p.T194M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000320031 |
| Start | 50075674:50075674(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1613T>G |
| AA Mutation | p.Val538Gly(p.V538G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000320031 |
| Start | 50071396:50071396(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs145459787 |
| CDS Mutation | c.837C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000320031 |
| Start | 50079165:50079165(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2490G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000320031 |
| Start | 50077058:50077058(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2007C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000320031 |
| Start | 50081405:50081405(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2916G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000320031 |
| Start | 50068134:50068134(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs756398910 |
| CDS Mutation | c.493C>T |
| AA Mutation | p.Arg165Ter(p.R165*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | frameshift_variant;splice_region_variant |
| Transcription ID | ENST00000320031 |
| Start | 50077378:50077379(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.2073dupC |
| AA Mutation | p.Gly692ArgfsTer6(p.G692Rfs*6) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000320031 |
| Start | 50080285:50080286(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.2737_2738dupTG |
| AA Mutation | p.Trp913CysfsTer3(p.W913Cfs*3) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | splice_donor_variant |
| Transcription ID | ENST00000320031 |
| Start | 50078126:50078126(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200623247 |
| CDS Mutation | c.2219+1G>A |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |