Primary Site >> Stomach Cancer
Gene >> ALDH1A2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000249750 |
| Start | 57992769:57992769(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs781766424 |
| CDS Mutation | c.734C>T |
| AA Mutation | p.Thr245Met(p.T245M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000249750 |
| Start | 57963932:57963932(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs778997757 |
| CDS Mutation | c.1039C>T |
| AA Mutation | p.Arg347Cys(p.R347C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000249750 |
| Start | 58065569:58065569(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.82T>C |
| AA Mutation | p.Ser28Pro(p.S28P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000249750 |
| Start | 57995086:57995086(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.547A>T |
| AA Mutation | p.Ile183Phe(p.I183F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000249750 |
| Start | 57993019:57993019(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.610G>T |
| AA Mutation | p.Gly204Cys(p.G204C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000249750 |
| Start | 58065588:58065588(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.63G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000249750 |
| Start | 58014240:58014240(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.159A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000249750 |
| Start | 57961211:57961211(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs768636227 |
| CDS Mutation | c.1335C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |