Primary Site >> Stomach Cancer
Gene >> ZNF160
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000418871 |
| Start | 53068417:53068417(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201073674 |
| CDS Mutation | c.2117G>A |
| AA Mutation | p.Arg706Gln(p.R706Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000418871 |
| Start | 53068721:53068721(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs757182149 |
| CDS Mutation | c.1813C>T |
| AA Mutation | p.Arg605Cys(p.R605C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000418871 |
| Start | 53069644:53069644(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs145414197 |
| CDS Mutation | c.890G>A |
| AA Mutation | p.Arg297His(p.R297H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000418871 |
| Start | 53069290:53069290(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1244A>G |
| AA Mutation | p.His415Arg(p.H415R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000418871 |
| Start | 53069327:53069327(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs367570319 |
| CDS Mutation | c.1207G>A |
| AA Mutation | p.Gly403Ser(p.G403S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000418871 |
| Start | 53068165:53068165(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2369A>C |
| AA Mutation | p.Lys790Thr(p.K790T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000418871 |
| Start | 53068385:53068385(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs747988442 |
| CDS Mutation | c.2149C>T |
| AA Mutation | p.Arg717Cys(p.R717C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000418871 |
| Start | 53069633:53069633(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs375230703 |
| CDS Mutation | c.901A>G |
| AA Mutation | p.Thr301Ala(p.T301A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000418871 |
| Start | 53069295:53069295(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1239A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000418871 |
| Start | 53068098:53068098(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs774506668 |
| CDS Mutation | c.2436C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000418871 |
| Start | 53074168:53074168(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs374134545 |
| CDS Mutation | c.243G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000418871 |
| Start | 53068887:53068887(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1647delA |
| AA Mutation | p.Lys549AsnfsTer60(p.K549Nfs*60) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000418871 |
| Start | 53068340:53068341(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | rs745909467 |
| CDS Mutation | c.2193dupA |
| AA Mutation | p.Pro732ThrfsTer5(p.P732Tfs*5) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |