Primary Site >> Stomach Cancer
Gene >> FOXA3
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000302177 |
| Start | 45872144:45872144(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.139A>G |
| AA Mutation | p.Ser47Gly(p.S47G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000302177 |
| Start | 45872264:45872264(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs752761784 |
| CDS Mutation | c.259A>G |
| AA Mutation | p.Ser87Gly(p.S87G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000302177 |
| Start | 45872843:45872843(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.838A>G |
| AA Mutation | p.Thr280Ala(p.T280A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000302177 |
| Start | 45872082:45872082(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs779323164 |
| CDS Mutation | c.77C>T |
| AA Mutation | p.Ser26Leu(p.S26L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000302177 |
| Start | 45872874:45872874(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.869G>A |
| AA Mutation | p.Gly290Glu(p.G290E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000302177 |
| Start | 45872258:45872258(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs543169864 |
| CDS Mutation | c.253G>A |
| AA Mutation | p.Gly85Ser(p.G85S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000302177 |
| Start | 45872281:45872281(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.276C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000302177 |
| Start | 45872730:45872730(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.729delC |
| AA Mutation | p.Ala244ArgfsTer49(p.A244Rfs*49) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000302177 |
| Start | 45872109:45872109(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.109delC |
| AA Mutation | p.Leu37SerfsTer5(p.L37Sfs*5) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000302177 |
| Start | 45872162:45872162(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.162delG |
| AA Mutation | p.Leu55SerfsTer84(p.L55Sfs*84) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000302177 |
| Start | 45872437:45872437(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.432C>G |
| AA Mutation | p.Tyr144Ter(p.Y144*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |