Primary Site >> Stomach Cancer
Gene >> ALOX12
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000251535 |
| Start | 7001741:7001741(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs143493293 |
| CDS Mutation | c.1091C>T |
| AA Mutation | p.Thr364Ile(p.T364I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000251535 |
| Start | 7000429:7000429(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs779986334 |
| CDS Mutation | c.901G>A |
| AA Mutation | p.Val301Ile(p.V301I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000251535 |
| Start | 7009984:7009984(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1670C>A |
| AA Mutation | p.Ala557Asp(p.A557D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000251535 |
| Start | 6999335:6999335(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.676G>A |
| AA Mutation | p.Glu226Lys(p.E226K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000251535 |
| Start | 7009998:7009998(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs768496365 |
| CDS Mutation | c.1684C>T |
| AA Mutation | p.Arg562Trp(p.R562W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000251535 |
| Start | 6998800:6998800(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs776908949 |
| CDS Mutation | c.505G>A |
| AA Mutation | p.Glu169Lys(p.E169K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000251535 |
| Start | 7005992:7005992(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1383C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |