Primary Site >> Stomach Cancer
Gene >> ALKBH1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000216489 |
| Start | 77674185:77674185(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs370283555 |
| CDS Mutation | c.797C>T |
| AA Mutation | p.Thr266Met(p.T266M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000216489 |
| Start | 77673882:77673882(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1100C>T |
| AA Mutation | p.Thr367Ile(p.T367I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000216489 |
| Start | 77707985:77707985(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.20C>T |
| AA Mutation | p.Ala7Val(p.A7V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000216489 |
| Start | 77679951:77679951(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.475C>T |
| AA Mutation | p.Arg159Trp(p.R159W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000216489 |
| Start | 77674053:77674053(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.929C>A |
| AA Mutation | p.Pro310His(p.P310H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000216489 |
| Start | 77694825:77694825(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.368C>G |
| AA Mutation | p.Ser123Cys(p.S123C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000216489 |
| Start | 77707882:77707882(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs780661069 |
| CDS Mutation | c.123A>C |
| AA Mutation | p.Glu41Asp(p.E41D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000216489 |
| Start | 77679921:77679921(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs764694107 |
| CDS Mutation | c.505C>T |
| AA Mutation | p.Arg169Cys(p.R169C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |