Primary Site >> Stomach Cancer
Gene >> NR4A1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000243050 |
| Start | 52054380:52054380(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs377043577 |
| CDS Mutation | c.52C>T |
| AA Mutation | p.Arg18Cys(p.R18C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000243050 |
| Start | 52054931:52054931(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.603C>A |
| AA Mutation | p.Ser201Arg(p.S201R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000243050 |
| Start | 52058709:52058709(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1562C>T |
| AA Mutation | p.Pro521Leu(p.P521L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000243050 |
| Start | 52054765:52054765(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.437T>G |
| AA Mutation | p.Phe146Cys(p.F146C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000243050 |
| Start | 52056030:52056030(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.877C>T |
| AA Mutation | p.Arg293Cys(p.R293C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000243050 |
| Start | 52056083:52056083(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.930T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000243050 |
| Start | 52057212:52057212(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1314G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000243050 |
| Start | 52056501:52056501(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1014A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000243050 |
| Start | 52057364:52057364(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs768492255 |
| CDS Mutation | c.1374C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |