Primary Site >> Stomach Cancer
Gene >> RPS6KA2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265678 |
| Start | 166419930:166419930(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs766805003 |
| CDS Mutation | c.1772C>T |
| AA Mutation | p.Ala591Val(p.A591V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265678 |
| Start | 166418338:166418338(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1825A>G |
| AA Mutation | p.Thr609Ala(p.T609A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265678 |
| Start | 166469854:166469854(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.959C>T |
| AA Mutation | p.Thr320Ile(p.T320I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265678 |
| Start | 166469872:166469872(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs759240466 |
| CDS Mutation | c.941G>A |
| AA Mutation | p.Arg314His(p.R314H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265678 |
| Start | 166531243:166531243(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.287C>A |
| AA Mutation | p.Ala96Asp(p.A96D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265678 |
| Start | 166423314:166423314(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1685G>A |
| AA Mutation | p.Arg562His(p.R562H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265678 |
| Start | 166488838:166488838(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.902G>A |
| AA Mutation | p.Arg301Gln(p.R301Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265678 |
| Start | 166430566:166430566(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs779109340 |
| CDS Mutation | c.1468C>T |
| AA Mutation | p.Arg490Cys(p.R490C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265678 |
| Start | 166430520:166430520(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs145694057 |
| CDS Mutation | c.1514C>T |
| AA Mutation | p.Ser505Leu(p.S505L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265678 |
| Start | 166451206:166451206(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1103A>G |
| AA Mutation | p.Asn368Ser(p.N368S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000265678 |
| Start | 166413860:166413860(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2010G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000265678 |
| Start | 166498619:166498619(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200188704 |
| CDS Mutation | c.636C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000265678 |
| Start | 166430519:166430519(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs140163975 |
| CDS Mutation | c.1515G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |