Primary Site >> Stomach Cancer
Gene >> VANGL2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368061 |
| Start | 160415898:160415898(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs765036390 |
| CDS Mutation | c.61C>T |
| AA Mutation | p.Arg21Cys(p.R21C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000368061 |
| Start | 160421054:160421054(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs778018773 |
| CDS Mutation | c.940A>C |
| AA Mutation | p.Asn314His(p.N314H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368061 |
| Start | 160425256:160425256(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs757893266 |
| CDS Mutation | c.1444C>T |
| AA Mutation | p.Arg482Cys(p.R482C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368061 |
| Start | 160419509:160419509(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.700G>A |
| AA Mutation | p.Val234Met(p.V234M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368061 |
| Start | 160416067:160416067(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs751467341 |
| CDS Mutation | c.77G>A |
| AA Mutation | p.Arg26His(p.R26H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368061 |
| Start | 160416109:160416109(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs141931627 |
| CDS Mutation | c.119G>A |
| AA Mutation | p.Gly40Glu(p.G40E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368061 |
| Start | 160419315:160419315(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.506G>A |
| AA Mutation | p.Arg169His(p.R169H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368061 |
| Start | 160419339:160419339(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.530G>A |
| AA Mutation | p.Arg177His(p.R177H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368061 |
| Start | 160424177:160424177(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1199G>A |
| AA Mutation | p.Arg400His(p.R400H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368061 |
| Start | 160419417:160419417(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs766519016 |
| CDS Mutation | c.608G>A |
| AA Mutation | p.Arg203His(p.R203H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000368061 |
| Start | 160419238:160419238(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs769374648 |
| CDS Mutation | c.429G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000368061 |
| Start | 160419472:160419472(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs374653941 |
| CDS Mutation | c.663G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |