Primary Site >> Stomach Cancer
Gene >> ATG14
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000247178 |
| Start | 55369702:55369702(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs144919020 |
| CDS Mutation | c.1396G>A |
| AA Mutation | p.Ala466Thr(p.A466T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000247178 |
| Start | 55369905:55369905(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs761765075 |
| CDS Mutation | c.1193G>A |
| AA Mutation | p.Arg398Gln(p.R398Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000247178 |
| Start | 55382185:55382185(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs767328468 |
| CDS Mutation | c.654C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000247178 |
| Start | 55369658:55369658(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs377499505 |
| CDS Mutation | c.1440G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000247178 |
| Start | 55380590:55380590(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.978C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000247178 |
| Start | 55369892:55369892(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs764423857 |
| CDS Mutation | c.1206G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |