Primary Site >> Stomach Cancer
Gene >> FDXR
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000293195 |
| Start | 74864254:74864254(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.896C>T |
| AA Mutation | p.Ala299Val(p.A299V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000293195 |
| Start | 74864048:74864048(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs376509346 |
| CDS Mutation | c.1022G>A |
| AA Mutation | p.Arg341His(p.R341H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000293195 |
| Start | 74863109:74863109(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1312T>C |
| AA Mutation | p.Tyr438His(p.Y438H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000293195 |
| Start | 74866821:74866821(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.233T>C |
| AA Mutation | p.Val78Ala(p.V78A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000293195 |
| Start | 74865754:74865754(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.574G>A |
| AA Mutation | p.Ala192Thr(p.A192T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000293195 |
| Start | 74863959:74863959(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs375884169 |
| CDS Mutation | c.1111G>A |
| AA Mutation | p.Val371Met(p.V371M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000293195 |
| Start | 74864224:74864224(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.926G>A |
| AA Mutation | p.Arg309Gln(p.R309Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000293195 |
| Start | 74865758:74865758(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200642785 |
| CDS Mutation | c.570C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |