Primary Site >> Stomach Cancer
Gene >> ZEB1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000320985 |
| Start | 31520885:31520885(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1550A>C |
| AA Mutation | p.Glu517Ala(p.E517A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000320985 |
| Start | 31520833:31520833(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1498A>G |
| AA Mutation | p.Thr500Ala(p.T500A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000320985 |
| Start | 31521583:31521583(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2248T>C |
| AA Mutation | p.Ser750Pro(p.S750P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000320985 |
| Start | 31520848:31520848(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1513A>G |
| AA Mutation | p.Ser505Gly(p.S505G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000320985 |
| Start | 31520759:31520759(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1424T>A |
| AA Mutation | p.Ile475Asn(p.I475N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000320985 |
| Start | 31523983:31523983(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2652G>C |
| AA Mutation | p.Gln884His(p.Q884H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000320985 |
| Start | 31527094:31527094(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3205G>A |
| AA Mutation | p.Glu1069Lys(p.E1069K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000320985 |
| Start | 31520891:31520891(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1556A>G |
| AA Mutation | p.Asp519Gly(p.D519G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000320985 |
| Start | 31510869:31510869(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.678A>C |
| AA Mutation | p.Arg226Ser(p.R226S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000320985 |
| Start | 31521897:31521897(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2562A>C |
| AA Mutation | p.Gln854His(p.Q854H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000320985 |
| Start | 31521713:31521713(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2378T>A |
| AA Mutation | p.Ile793Asn(p.I793N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000320985 |
| Start | 31526959:31526959(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3070G>A |
| AA Mutation | p.Glu1024Lys(p.E1024K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000320985 |
| Start | 31502393:31502393(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs749371907 |
| CDS Mutation | c.365A>G |
| AA Mutation | p.His122Arg(p.H122R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000320985 |
| Start | 31527133:31527133(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3244A>G |
| AA Mutation | p.Asn1082Asp(p.N1082D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000320985 |
| Start | 31319289:31319289(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.55A>G |
| AA Mutation | p.Asn19Asp(p.N19D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000320985 |
| Start | 31520838:31520838(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1503C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000320985 |
| Start | 31526994:31526994(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3105C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000320985 |
| Start | 31526880:31526880(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2991G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000320985 |
| Start | 31520130:31520130(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs746581968 |
| CDS Mutation | c.795G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000320985 |
| Start | 31527039:31527039(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3150G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000320985 |
| Start | 31521897:31521897(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs755654045 |
| CDS Mutation | c.2562A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |