Primary Site >> Stomach Cancer
Gene >> FOXI1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000306268 |
| Start | 170106354:170106354(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.397G>A |
| AA Mutation | p.Ala133Thr(p.A133T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000306268 |
| Start | 170106333:170106333(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.376T>C |
| AA Mutation | p.Tyr126His(p.Y126H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000306268 |
| Start | 170108087:170108087(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.613A>C |
| AA Mutation | p.Lys205Gln(p.K205Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000306268 |
| Start | 170106304:170106304(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.347A>C |
| AA Mutation | p.Glu116Ala(p.E116A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000306268 |
| Start | 170108255:170108255(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.781A>G |
| AA Mutation | p.Thr261Ala(p.T261A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000306268 |
| Start | 170108490:170108490(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1016A>C |
| AA Mutation | p.Asn339Thr(p.N339T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000306268 |
| Start | 170108491:170108491(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1017C>A |
| AA Mutation | p.Asn339Lys(p.N339K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000306268 |
| Start | 170106036:170106036(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs781004930 |
| CDS Mutation | c.79G>A |
| AA Mutation | p.Glu27Lys(p.E27K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000306268 |
| Start | 170108049:170108049(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.575G>A |
| AA Mutation | p.Gly192Asp(p.G192D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000306268 |
| Start | 170108152:170108152(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.678A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000306268 |
| Start | 170106113:170106113(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.156C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000306268 |
| Start | 170106107:170106107(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.155delG |
| AA Mutation | p.Gly52AlafsTer19(p.G52Afs*19) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000306268 |
| Start | 170106030:170106030(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.78delC |
| AA Mutation | p.Glu27ArgfsTer2(p.E27Rfs*2) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000306268 |
| Start | 170108345:170108345(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs767090333 |
| CDS Mutation | c.876delG |
| AA Mutation | p.Ser293AlafsTer12(p.S293Afs*12) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000306268 |
| Start | 170106380:170106381(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.425dupA |
| AA Mutation | p.Arg143AlafsTer62(p.R143Afs*62) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |