Primary Site >> Stomach Cancer
Gene >> RORC
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000318247 |
| Start | 151813039:151813039(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1193G>A |
| AA Mutation | p.Ser398Asn(p.S398N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000318247 |
| Start | 151815263:151815263(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.461C>T |
| AA Mutation | p.Pro154Leu(p.P154L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000318247 |
| Start | 151813596:151813596(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.958T>C |
| AA Mutation | p.Cys320Arg(p.C320R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000318247 |
| Start | 151813314:151813314(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1099C>T |
| AA Mutation | p.Arg367Trp(p.R367W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000318247 |
| Start | 151813265:151813265(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1148G>A |
| AA Mutation | p.Gly383Asp(p.G383D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000318247 |
| Start | 151815352:151815352(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.372G>C |
| AA Mutation | p.Gln124His(p.Q124H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000318247 |
| Start | 151813293:151813293(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs750446790 |
| CDS Mutation | c.1120C>T |
| AA Mutation | p.Arg374Cys(p.R374C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |