Primary Site >> Stomach Cancer
Gene >> RNF168
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000318037 |
| Start | 196503064:196503064(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.110A>G |
| AA Mutation | p.Lys37Arg(p.K37R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000318037 |
| Start | 196488641:196488641(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.344A>G |
| AA Mutation | p.Glu115Gly(p.E115G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000318037 |
| Start | 196483851:196483851(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.599A>G |
| AA Mutation | p.Asn200Ser(p.N200S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000318037 |
| Start | 196472104:196472104(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs143993777 |
| CDS Mutation | c.1431C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000318037 |
| Start | 196472353:196472353(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1182C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000318037 |
| Start | 196471894:196471894(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1641C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000318037 |
| Start | 196472139:196472139(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1396C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000318037 |
| Start | 196472617:196472617(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs781641742 |
| CDS Mutation | c.918C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000318037 |
| Start | 196487477:196487480(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs771720993 |
| CDS Mutation | c.477_480delACAG |
| AA Mutation | p.Ala161LysfsTer11(p.A161Kfs*11) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000318037 |
| Start | 196487545:196487545(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs375915880 |
| CDS Mutation | c.412G>T |
| AA Mutation | p.Glu138Ter(p.E138*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000318037 |
| Start | 196472365:196472366(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.1169dupA |
| AA Mutation | p.Asn390LysfsTer7(p.N390Kfs*7) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000318037 |
| Start | 196471853:196471854(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.1681dupA |
| AA Mutation | p.Ser561LysfsTer21(p.S561Kfs*21) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |