Primary Site >> Stomach Cancer
Gene >> RPS6KA3
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379565 |
| Start | 20177031:20177031(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.899G>A |
| AA Mutation | p.Arg300Gln(p.R300Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379565 |
| Start | 20234806:20234806(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.78G>T |
| AA Mutation | p.Gln26His(p.Q26H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379565 |
| Start | 20177020:20177020(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.910A>G |
| AA Mutation | p.Lys304Glu(p.K304E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379565 |
| Start | 20172859:20172859(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1240A>G |
| AA Mutation | p.Asn414Asp(p.N414D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379565 |
| Start | 20155487:20155487(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2134C>T |
| AA Mutation | p.Arg712Cys(p.R712C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000379565 |
| Start | 20187852:20187852(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.750C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000379565 |
| Start | 20204043:20204043(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs757971865 |
| CDS Mutation | c.304T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000379565 |
| Start | 20155417:20155418(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.2203dupA |
| AA Mutation | p.Ile735AsnfsTer9(p.I735Nfs*9) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |