Primary Site >> Stomach Cancer
Gene >> CRY1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000008527 |
| Start | 106999753:106999753(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.935A>C |
| AA Mutation | p.Asn312Thr(p.N312T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000008527 |
| Start | 107022121:107022121(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200714794 |
| CDS Mutation | c.230G>A |
| AA Mutation | p.Arg77His(p.R77H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000008527 |
| Start | 107001918:107001918(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.441T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000008527 |
| Start | 106992823:106992823(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1725T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000008527 |
| Start | 106997343:106997343(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1536C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000008527 |
| Start | 107000001:107000001(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs767156491 |
| CDS Mutation | c.766C>T |
| AA Mutation | p.Arg256Ter(p.R256*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | stop_gained;splice_region_variant |
| Transcription ID | ENST00000008527 |
| Start | 107092805:107092805(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.157C>T |
| AA Mutation | p.Arg53Ter(p.R53*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000008527 |
| Start | 106999589:106999589(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs753452380 |
| CDS Mutation | c.1099C>T |
| AA Mutation | p.Arg367Ter(p.R367*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |