Primary Site >> Stomach Cancer
Gene >> CPEB1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000615198 |
| Start | 82553481:82553481(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1049G>A |
| AA Mutation | p.Arg350Gln(p.R350Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000615198 |
| Start | 82627359:82627359(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.24A>C |
| AA Mutation | p.Glu8Asp(p.E8D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000615198 |
| Start | 82571478:82571478(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs374422926 |
| CDS Mutation | c.245C>T |
| AA Mutation | p.Ala82Val(p.A82V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000615198 |
| Start | 82549522:82549522(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1337A>C |
| AA Mutation | p.Asn446Thr(p.N446T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000615198 |
| Start | 82549595:82549595(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1264G>T |
| AA Mutation | p.Asp422Tyr(p.D422Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000615198 |
| Start | 82549487:82549487(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1372G>T |
| AA Mutation | p.Asp458Tyr(p.D458Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000615198 |
| Start | 82549571:82549571(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1288G>A |
| AA Mutation | p.Gly430Ser(p.G430S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000615198 |
| Start | 82549635:82549635(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1224A>C |
| AA Mutation | p.Leu408Phe(p.L408F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000615198 |
| Start | 82547185:82547185(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs374011661 |
| CDS Mutation | c.1452C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000615198 |
| Start | 82627338:82627338(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.45C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000615198 |
| Start | 82552597:82552597(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs754255400 |
| CDS Mutation | c.1083C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000615198 |
| Start | 82549590:82549590(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1269C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000615198 |
| Start | 82544627:82544627(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1651delC |
| AA Mutation | p.Leu551Ter(p.L551*) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |