Primary Site >> Stomach Cancer
Gene >> CPEB4
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265085 |
| Start | 173956106:173956106(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2159G>A |
| AA Mutation | p.Arg720His(p.R720H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265085 |
| Start | 173890791:173890791(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1058C>T |
| AA Mutation | p.Ser353Phe(p.S353F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265085 |
| Start | 173949541:173949541(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1490C>A |
| AA Mutation | p.Pro497His(p.P497H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265085 |
| Start | 173951841:173951841(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1683G>T |
| AA Mutation | p.Trp561Cys(p.W561C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265085 |
| Start | 173932453:173932453(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs142106976 |
| CDS Mutation | c.1211G>A |
| AA Mutation | p.Arg404His(p.R404H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265085 |
| Start | 173953256:173953256(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1946G>A |
| AA Mutation | p.Gly649Glu(p.G649E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265085 |
| Start | 173949577:173949577(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1526A>G |
| AA Mutation | p.Lys509Arg(p.K509R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265085 |
| Start | 173890431:173890431(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.698A>G |
| AA Mutation | p.His233Arg(p.H233R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265085 |
| Start | 173890323:173890323(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs760479707 |
| CDS Mutation | c.590C>T |
| AA Mutation | p.Ala197Val(p.A197V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000265085 |
| Start | 173890678:173890678(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.945A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000265085 |
| Start | 173890504:173890504(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.771T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000265085 |
| Start | 173951880:173951880(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1722G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000265085 |
| Start | 173953101:173953101(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs770312805 |
| CDS Mutation | c.1791G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000265085 |
| Start | 173890105:173890105(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.372G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000265085 |
| Start | 173956098:173956098(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs746507891 |
| CDS Mutation | c.2151C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |