Primary Site >> Stomach Cancer
Gene >> VIL1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000248444 |
| Start | 218437298:218437298(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2146C>A |
| AA Mutation | p.Pro716Thr(p.P716T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000248444 |
| Start | 218430797:218430797(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs150670051 |
| CDS Mutation | c.1021G>A |
| AA Mutation | p.Val341Ile(p.V341I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000248444 |
| Start | 218437218:218437218(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs145276026 |
| CDS Mutation | c.2066G>A |
| AA Mutation | p.Arg689His(p.R689H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000248444 |
| Start | 218427970:218427970(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.353G>A |
| AA Mutation | p.Arg118Gln(p.R118Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000248444 |
| Start | 218429432:218429432(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.715G>A |
| AA Mutation | p.Ala239Thr(p.A239T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000248444 |
| Start | 218425791:218425791(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.327C>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000248444 |
| Start | 218432840:218432840(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs139447471 |
| CDS Mutation | c.1389C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000248444 |
| Start | 218430874:218430874(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs376351268 |
| CDS Mutation | c.1098C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |