Primary Site >> Stomach Cancer
Gene >> PER1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000317276 |
| Start | 8143843:8143843(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs753761027 |
| CDS Mutation | c.2495G>A |
| AA Mutation | p.Arg832Gln(p.R832Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000317276 |
| Start | 8146983:8146983(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1649G>C |
| AA Mutation | p.Cys550Ser(p.C550S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000317276 |
| Start | 8143810:8143810(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs370403552 |
| CDS Mutation | c.2528G>A |
| AA Mutation | p.Arg843His(p.R843H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000317276 |
| Start | 8150008:8150008(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs372671656 |
| CDS Mutation | c.492G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000317276 |
| Start | 8143782:8143782(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs770790365 |
| CDS Mutation | c.2556G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000317276 |
| Start | 8143454:8143454(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.2884delG |
| AA Mutation | p.Ala962ProfsTer160(p.A962Pfs*160) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |