Primary Site >> Stomach Cancer
Gene >> ALDH2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261733 |
| Start | 111798169:111798169(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200738174 |
| CDS Mutation | c.1175C>T |
| AA Mutation | p.Ala392Val(p.A392V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261733 |
| Start | 111781969:111781969(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.166A>G |
| AA Mutation | p.Thr56Ala(p.T56A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261733 |
| Start | 111783221:111783221(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs140919090 |
| CDS Mutation | c.283C>T |
| AA Mutation | p.Arg95Cys(p.R95C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000261733 |
| Start | 111783297:111783297(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.359C>T |
| AA Mutation | p.Ala120Val(p.A120V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261733 |
| Start | 111800051:111800051(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs757893333 |
| CDS Mutation | c.1394C>T |
| AA Mutation | p.Ala465Val(p.A465V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000261733 |
| Start | 111792114:111792114(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.849C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000261733 |
| Start | 111781971:111781971(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.168C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000261733 |
| Start | 111791365:111791365(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs111277749 |
| CDS Mutation | c.741C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000261733 |
| Start | 111792123:111792123(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs775259976 |
| CDS Mutation | c.864delG |
| AA Mutation | p.Lys289ArgfsTer122(p.K289Rfs*122) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |