Primary Site >> Stomach Cancer
Gene >> FOLR3
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000611028 |
| Start | 72136032:72136032(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.80C>T |
| AA Mutation | p.Ala27Val(p.A27V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000611028 |
| Start | 72139812:72139812(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs374758856 |
| CDS Mutation | c.719G>A |
| AA Mutation | p.Arg240His(p.R240H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000611028 |
| Start | 72135957:72135957(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5A>G |
| AA Mutation | p.Asp2Gly(p.D2G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000611028 |
| Start | 72136044:72136044(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs371010355 |
| CDS Mutation | c.92C>T |
| AA Mutation | p.Thr31Met(p.T31M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000611028 |
| Start | 72139775:72139775(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.682T>G |
| AA Mutation | p.Phe228Val(p.F228V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000611028 |
| Start | 72138992:72138992(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs371900505 |
| CDS Mutation | c.200C>T |
| AA Mutation | p.Thr67Met(p.T67M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000611028 |
| Start | 72138987:72138987(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.195C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000611028 |
| Start | 72139786:72139786(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs189330558 |
| CDS Mutation | c.693G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |