Primary Site >> Stomach Cancer
Gene >> RARG
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000425354 |
| Start | 53215705:53215705(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.274G>A |
| AA Mutation | p.Val92Met(p.V92M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000425354 |
| Start | 53213102:53213102(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs776186919 |
| CDS Mutation | c.1160G>A |
| AA Mutation | p.Arg387Gln(p.R387Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000425354 |
| Start | 53227447:53227447(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.99C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000425354 |
| Start | 53213641:53213641(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.873G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000425354 |
| Start | 53214131:53214131(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.741G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000425354 |
| Start | 53227435:53227435(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs779645994 |
| CDS Mutation | c.111G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000425354 |
| Start | 53227501:53227501(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.45delG |
| AA Mutation | p.Pro16LeufsTer27(p.P16Lfs*27) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |