Primary Site >> Stomach Cancer
Gene >> ZNF148
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360647 |
| Start | 125313574:125313574(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.67T>C |
| AA Mutation | p.Ser23Pro(p.S23P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360647 |
| Start | 125233632:125233632(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1094C>T |
| AA Mutation | p.Ala365Val(p.A365V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360647 |
| Start | 125313628:125313628(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.13G>A |
| AA Mutation | p.Asp5Asn(p.D5N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360647 |
| Start | 125234275:125234275(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.722A>C |
| AA Mutation | p.His241Pro(p.H241P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360647 |
| Start | 125233109:125233109(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1617G>T |
| AA Mutation | p.Glu539Asp(p.E539D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360647 |
| Start | 125232526:125232526(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2200C>T |
| AA Mutation | p.Arg734Cys(p.R734C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360647 |
| Start | 125233312:125233312(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1414A>G |
| AA Mutation | p.Lys472Glu(p.K472E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360647 |
| Start | 125232814:125232814(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1912C>T |
| AA Mutation | p.Pro638Ser(p.P638S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000360647 |
| Start | 125288223:125288223(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs529285699 |
| CDS Mutation | c.339C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000360647 |
| Start | 125233517:125233517(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1209G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000360647 |
| Start | 125313375:125313375(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.266delA |
| AA Mutation | p.Asn89MetfsTer24(p.N89Mfs*24) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000360647 |
| Start | 125233904:125233904(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.822delA |
| AA Mutation | p.Lys274AsnfsTer12(p.K274Nfs*12) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000360647 |
| Start | 125233873:125233874(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.852dupA |
| AA Mutation | p.Leu285ThrfsTer3(p.L285Tfs*3) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |