Primary Site >> Stomach Cancer
Gene >> RGS5
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000313961 |
| Start | 163161947:163161947(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs754717880 |
| CDS Mutation | c.185G>A |
| AA Mutation | p.Arg62His(p.R62H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000313961 |
| Start | 163161960:163161960(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.172G>A |
| AA Mutation | p.Ala58Thr(p.A58T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000313961 |
| Start | 163147374:163147374(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs112323155 |
| CDS Mutation | c.514C>T |
| AA Mutation | p.Arg172Cys(p.R172C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000313961 |
| Start | 163147457:163147457(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.431T>G |
| AA Mutation | p.Val144Gly(p.V144G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000313961 |
| Start | 163147428:163147428(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.460G>A |
| AA Mutation | p.Ala154Thr(p.A154T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000313961 |
| Start | 163161964:163161964(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs777324995 |
| CDS Mutation | c.168C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000313961 |
| Start | 163161971:163161971(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.161C>A |
| AA Mutation | p.Ser54Ter(p.S54*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |