Primary Site >> Stomach Cancer
Gene >> RARA
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000254066 |
| Start | 40352349:40352349(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.649C>G |
| AA Mutation | p.Arg217Gly(p.R217G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000254066 |
| Start | 40349824:40349824(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.368C>T |
| AA Mutation | p.Thr123Met(p.T123M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000254066 |
| Start | 40352350:40352350(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.650G>C |
| AA Mutation | p.Arg217Pro(p.R217P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000254066 |
| Start | 40354401:40354401(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.907G>A |
| AA Mutation | p.Gly303Ser(p.G303S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000254066 |
| Start | 40355311:40355311(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1061C>A |
| AA Mutation | p.Pro354Gln(p.P354Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000254066 |
| Start | 40349871:40349871(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.415C>A |
| AA Mutation | p.Arg139Ser(p.R139S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000254066 |
| Start | 40331329:40331329(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs376736940 |
| CDS Mutation | c.111G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |