Primary Site >> Stomach Cancer
Gene >> RHO
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000296271 |
| Start | 129533696:129533696(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs183318466 |
| CDS Mutation | c.1025C>T |
| AA Mutation | p.Thr342Met(p.T342M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000296271 |
| Start | 129529028:129529028(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.295C>A |
| AA Mutation | p.Leu99Met(p.L99M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000296271 |
| Start | 129532742:129532742(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.906C>A |
| AA Mutation | p.Asn302Lys(p.N302K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000296271 |
| Start | 129528938:129528938(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs761101263 |
| CDS Mutation | c.205C>T |
| AA Mutation | p.Arg69Cys(p.R69C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000296271 |
| Start | 129531031:129531031(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs139731264 |
| CDS Mutation | c.517G>A |
| AA Mutation | p.Ala173Thr(p.A173T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000296271 |
| Start | 129532661:129532661(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.825C>G |
| AA Mutation | p.Ile275Met(p.I275M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000296271 |
| Start | 129532695:129532695(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.859T>G |
| AA Mutation | p.Phe287Val(p.F287V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000296271 |
| Start | 129532602:129532602(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.766A>C |
| AA Mutation | p.Ile256Leu(p.I256L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000296271 |
| Start | 129532615:129532615(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.779C>T |
| AA Mutation | p.Ala260Val(p.A260V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000296271 |
| Start | 129533612:129533612(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs753609310 |
| CDS Mutation | c.941G>A |
| AA Mutation | p.Arg314Gln(p.R314Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |