Primary Site >> Stomach Cancer
Gene >> VPS33A
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000267199 |
| Start | 122251027:122251027(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.556T>C |
| AA Mutation | p.Tyr186His(p.Y186H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000267199 |
| Start | 122263660:122263660(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs150472752 |
| CDS Mutation | c.208C>T |
| AA Mutation | p.Arg70Cys(p.R70C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000267199 |
| Start | 122266389:122266389(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.20A>G |
| AA Mutation | p.Tyr7Cys(p.Y7C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000267199 |
| Start | 122261325:122261325(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.419A>G |
| AA Mutation | p.Tyr140Cys(p.Y140C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000267199 |
| Start | 122266401:122266401(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs765189927 |
| CDS Mutation | c.8C>T |
| AA Mutation | p.Ala3Val(p.A3V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000267199 |
| Start | 122235861:122235861(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs752623476 |
| CDS Mutation | c.1365G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |