Primary Site >> Stomach Cancer
Gene >> ZNF135
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000313434 |
| Start | 58067719:58067719(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1235G>A |
| AA Mutation | p.Cys412Tyr(p.C412Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000313434 |
| Start | 58066945:58066945(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs746765542 |
| CDS Mutation | c.461C>T |
| AA Mutation | p.Thr154Met(p.T154M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000313434 |
| Start | 58068016:58068016(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1532A>G |
| AA Mutation | p.Lys511Arg(p.K511R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000313434 |
| Start | 58066992:58066992(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.508A>C |
| AA Mutation | p.Ser170Arg(p.S170R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000313434 |
| Start | 58067580:58067580(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1096A>C |
| AA Mutation | p.Ser366Arg(p.S366R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000313434 |
| Start | 58063458:58063458(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs371178818 |
| CDS Mutation | c.173C>T |
| AA Mutation | p.Pro58Leu(p.P58L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000313434 |
| Start | 58067145:58067145(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.661A>G |
| AA Mutation | p.Lys221Glu(p.K221E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000313434 |
| Start | 58067524:58067524(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1040T>A |
| AA Mutation | p.Ile347Asn(p.I347N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000313434 |
| Start | 58067239:58067239(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs769862321 |
| CDS Mutation | c.755G>A |
| AA Mutation | p.Arg252Gln(p.R252Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000313434 |
| Start | 58068015:58068015(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1531A>G |
| AA Mutation | p.Lys511Glu(p.K511E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000313434 |
| Start | 58061696:58061696(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.150G>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000313434 |
| Start | 58063531:58063531(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs750077100 |
| CDS Mutation | c.246C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |