Primary Site >> Stomach Cancer
Gene >> PER2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000254657 |
| Start | 238258519:238258519(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1753A>G |
| AA Mutation | p.Ser585Gly(p.S585G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000254657 |
| Start | 238268091:238268091(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.932T>G |
| AA Mutation | p.Leu311Arg(p.L311R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000254657 |
| Start | 238258515:238258515(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1757G>T |
| AA Mutation | p.Cys586Phe(p.C586F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000254657 |
| Start | 238253568:238253568(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs199933426 |
| CDS Mutation | c.2455G>A |
| AA Mutation | p.Ala819Thr(p.A819T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000254657 |
| Start | 238253574:238253574(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2449G>A |
| AA Mutation | p.Val817Met(p.V817M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000254657 |
| Start | 238253025:238253025(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2998C>T |
| AA Mutation | p.Pro1000Ser(p.P1000S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000254657 |
| Start | 238253205:238253205(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2818G>C |
| AA Mutation | p.Glu940Gln(p.E940Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000254657 |
| Start | 238253686:238253686(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2337A>T |
| AA Mutation | p.Arg779Ser(p.R779S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000254657 |
| Start | 238253687:238253687(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2336G>A |
| AA Mutation | p.Arg779Lys(p.R779K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000254657 |
| Start | 238262294:238262294(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs775687700 |
| CDS Mutation | c.1204G>T |
| AA Mutation | p.Ala402Ser(p.A402S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000254657 |
| Start | 238255725:238255725(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2252T>C |
| AA Mutation | p.Leu751Pro(p.L751P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000254657 |
| Start | 238253385:238253385(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2638G>A |
| AA Mutation | p.Ala880Thr(p.A880T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000254657 |
| Start | 238250636:238250636(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3382A>G |
| AA Mutation | p.Ile1128Val(p.I1128V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000254657 |
| Start | 238273071:238273071(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.569C>T |
| AA Mutation | p.Ala190Val(p.A190V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000254657 |
| Start | 238253062:238253062(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs768386498 |
| CDS Mutation | c.2961G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000254657 |
| Start | 238277853:238277853(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.84G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000254657 |
| Start | 238253575:238253575(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs146565410 |
| CDS Mutation | c.2448C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000254657 |
| Start | 238251717:238251717(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs771960253 |
| CDS Mutation | c.3156G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |