Primary Site >> Stomach Cancer
Gene >> ZNF569
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000316950 |
| Start | 37413481:37413481(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1177C>G |
| AA Mutation | p.Gln393Glu(p.Q393E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000316950 |
| Start | 37412804:37412804(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1854C>A |
| AA Mutation | p.Ser618Arg(p.S618R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000316950 |
| Start | 37412796:37412796(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1862T>G |
| AA Mutation | p.Leu621Arg(p.L621R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000316950 |
| Start | 37412755:37412755(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs199656641 |
| CDS Mutation | c.1903G>A |
| AA Mutation | p.Asp635Asn(p.D635N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000316950 |
| Start | 37413643:37413643(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1015G>A |
| AA Mutation | p.Ala339Thr(p.A339T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000316950 |
| Start | 37413025:37413025(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1633A>G |
| AA Mutation | p.Thr545Ala(p.T545A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000316950 |
| Start | 37412770:37412770(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1888G>A |
| AA Mutation | p.Gly630Ser(p.G630S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000316950 |
| Start | 37413875:37413875(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.783A>C |
| AA Mutation | p.Gln261His(p.Q261H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000316950 |
| Start | 37413597:37413597(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1061A>T |
| AA Mutation | p.Tyr354Phe(p.Y354F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000316950 |
| Start | 37413262:37413262(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1396T>C |
| AA Mutation | p.Tyr466His(p.Y466H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000316950 |
| Start | 37412771:37412771(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1887A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000316950 |
| Start | 37426331:37426331(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.63G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000316950 |
| Start | 37412885:37412885(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1773T>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000316950 |
| Start | 37414237:37414237(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.421T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000316950 |
| Start | 37413083:37413083(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1575T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000316950 |
| Start | 37413015:37413015(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1643delA |
| AA Mutation | p.Lys548SerfsTer22(p.K548Sfs*22) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000316950 |
| Start | 37414269:37414269(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.389delT |
| AA Mutation | p.Phe130SerfsTer17(p.F130Sfs*17) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000316950 |
| Start | 37414051:37414051(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.607A>T |
| AA Mutation | p.Arg203Ter(p.R203*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000316950 |
| Start | 37413596:37413596(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1062T>A |
| AA Mutation | p.Tyr354Ter(p.Y354*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000316950 |
| Start | 37414268:37414269(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | rs752923644 |
| CDS Mutation | c.389dupT |
| AA Mutation | p.Ser132PhefsTer7(p.S132Ffs*7) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |