Primary Site >> Stomach Cancer
Gene >> RPS6KA1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000374168 |
| Start | 26557011:26557011(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs779820707 |
| CDS Mutation | c.995G>A |
| AA Mutation | p.Arg332His(p.R332H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000374168 |
| Start | 26555164:26555164(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs766775987 |
| CDS Mutation | c.770C>T |
| AA Mutation | p.Thr257Met(p.T257M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000374168 |
| Start | 26561661:26561661(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs760553222 |
| CDS Mutation | c.1588G>C |
| AA Mutation | p.Gly530Arg(p.G530R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000374168 |
| Start | 26561632:26561632(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1559G>A |
| AA Mutation | p.Gly520Asp(p.G520D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000374168 |
| Start | 26551698:26551698(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.443A>T |
| AA Mutation | p.Asp148Val(p.D148V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000374168 |
| Start | 26561581:26561581(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs748782890 |
| CDS Mutation | c.1508G>A |
| AA Mutation | p.Arg503Gln(p.R503Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000374168 |
| Start | 26555167:26555167(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.773G>A |
| AA Mutation | p.Gly258Asp(p.G258D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000374168 |
| Start | 26557009:26557009(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs749911377 |
| CDS Mutation | c.993T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000374168 |
| Start | 26551648:26551648(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.393C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000374168 |
| Start | 26571905:26571905(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1809G>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000374168 |
| Start | 26572194:26572194(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs371025431 |
| CDS Mutation | c.1848C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |