Primary Site >> Stomach Cancer
Gene >> DECR2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000219481 |
| Start | 407459:407459(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs141623402 |
| CDS Mutation | c.236G>A |
| AA Mutation | p.Arg79His(p.R79H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000219481 |
| Start | 407533:407533(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.310T>C |
| AA Mutation | p.Phe104Leu(p.F104L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000219481 |
| Start | 411481:411481(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs367552533 |
| CDS Mutation | c.782C>T |
| AA Mutation | p.Thr261Met(p.T261M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000219481 |
| Start | 411435:411435(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs777162278 |
| CDS Mutation | c.736G>A |
| AA Mutation | p.Ala246Thr(p.A246T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000219481 |
| Start | 411554:411554(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.855C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000219481 |
| Start | 411404:411404(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs553093118 |
| CDS Mutation | c.705G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |