Primary Site >> Stomach Cancer
Gene >> FOXL2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000330315 |
| Start | 138946376:138946376(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.347C>A |
| AA Mutation | p.Pro116Gln(p.P116Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000330315 |
| Start | 138946611:138946611(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.112G>A |
| AA Mutation | p.Gly38Ser(p.G38S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000330315 |
| Start | 138945704:138945704(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1019C>T |
| AA Mutation | p.Ala340Val(p.A340V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000330315 |
| Start | 138945669:138945669(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1054G>A |
| AA Mutation | p.Glu352Lys(p.E352K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000330315 |
| Start | 138946596:138946596(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.127G>A |
| AA Mutation | p.Gly43Arg(p.G43R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000330315 |
| Start | 138946308:138946308(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.415G>A |
| AA Mutation | p.Glu139Lys(p.E139K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000330315 |
| Start | 138946397:138946397(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.326A>G |
| AA Mutation | p.Asn109Ser(p.N109S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000330315 |
| Start | 138946254:138946254(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs758370933 |
| CDS Mutation | c.469C>G |
| AA Mutation | p.Pro157Ala(p.P157A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000330315 |
| Start | 138946285:138946285(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs781285704 |
| CDS Mutation | c.438C>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |