Primary Site >> Stomach Cancer
Gene >> NR4A3
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000395097 |
| Start | 99828095:99828095(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.53C>T |
| AA Mutation | p.Ala18Val(p.A18V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000395097 |
| Start | 99828937:99828937(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.895G>A |
| AA Mutation | p.Ala299Thr(p.A299T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000395097 |
| Start | 99828197:99828197(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.155C>A |
| AA Mutation | p.Thr52Asn(p.T52N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000395097 |
| Start | 99828200:99828200(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.158C>T |
| AA Mutation | p.Thr53Met(p.T53M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000395097 |
| Start | 99828375:99828375(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.333G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000395097 |
| Start | 99828504:99828504(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs775860896 |
| CDS Mutation | c.462G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |