Primary Site >> Stomach Cancer
Gene >> RPSA
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000301821 |
| Start | 39410897:39410897(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.396G>T |
| AA Mutation | p.Gln132His(p.Q132H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000301821 |
| Start | 39411721:39411721(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.571C>T |
| AA Mutation | p.Arg191Cys(p.R191C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000301821 |
| Start | 39411722:39411722(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.572G>A |
| AA Mutation | p.Arg191His(p.R191H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000301821 |
| Start | 39411710:39411710(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.560G>A |
| AA Mutation | p.Gly187Asp(p.G187D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000301821 |
| Start | 39410830:39410830(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.329A>T |
| AA Mutation | p.Asn110Ile(p.N110I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000301821 |
| Start | 39407762:39407762(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.109T>C |
| AA Mutation | p.Tyr37His(p.Y37H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000301821 |
| Start | 39411707:39411707(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.557G>A |
| AA Mutation | p.Arg186His(p.R186H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000301821 |
| Start | 39410939:39410939(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200785492 |
| CDS Mutation | c.438G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |