Primary Site >> Stomach Cancer
Gene >> FILIP1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000237172 |
| Start | 75314681:75314681(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs147080592 |
| CDS Mutation | c.1151G>A |
| AA Mutation | p.Arg384Gln(p.R384Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000237172 |
| Start | 75314832:75314832(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1000A>G |
| AA Mutation | p.Lys334Glu(p.K334E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000237172 |
| Start | 75308695:75308695(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3638G>A |
| AA Mutation | p.Gly1213Asp(p.G1213D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000237172 |
| Start | 75414843:75414843(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.130A>G |
| AA Mutation | p.Arg44Gly(p.R44G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000237172 |
| Start | 75353678:75353678(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs770696243 |
| CDS Mutation | c.490C>T |
| AA Mutation | p.Arg164Cys(p.R164C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000237172 |
| Start | 75313946:75313946(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1886T>C |
| AA Mutation | p.Ile629Thr(p.I629T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000237172 |
| Start | 75314136:75314136(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1696T>C |
| AA Mutation | p.Tyr566His(p.Y566H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000237172 |
| Start | 75312737:75312737(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs766680260 |
| CDS Mutation | c.3095T>A |
| AA Mutation | p.Met1032Lys(p.M1032K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000237172 |
| Start | 75362874:75362874(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.320A>C |
| AA Mutation | p.Lys107Thr(p.K107T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000237172 |
| Start | 75312809:75312809(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3023A>G |
| AA Mutation | p.Gln1008Arg(p.Q1008R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000237172 |
| Start | 75313359:75313359(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs755925479 |
| CDS Mutation | c.2473C>T |
| AA Mutation | p.Arg825Trp(p.R825W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000237172 |
| Start | 75313088:75313088(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs554789463 |
| CDS Mutation | c.2744C>T |
| AA Mutation | p.Thr915Ile(p.T915I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000237172 |
| Start | 75313413:75313413(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2419A>T |
| AA Mutation | p.Thr807Ser(p.T807S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000237172 |
| Start | 75353605:75353605(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.563A>T |
| AA Mutation | p.His188Leu(p.H188L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000237172 |
| Start | 75313342:75313342(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2490A>T |
| AA Mutation | p.Glu830Asp(p.E830D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000237172 |
| Start | 75315018:75315018(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.814A>G |
| AA Mutation | p.Thr272Ala(p.T272A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000237172 |
| Start | 75312433:75312433(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3399G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000237172 |
| Start | 75315126:75315126(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs373722500 |
| CDS Mutation | c.706C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000237172 |
| Start | 75308877:75308877(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3456C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000237172 |
| Start | 75314764:75314764(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1068G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000237172 |
| Start | 75353631:75353631(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.537C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000237172 |
| Start | 75315145:75315145(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.687T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000237172 |
| Start | 75313198:75313198(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2634C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000237172 |
| Start | 75313441:75313441(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs368729229 |
| CDS Mutation | c.2391T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000237172 |
| Start | 75414860:75414860(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.113delA |
| AA Mutation | p.Lys38ArgfsTer22(p.K38Rfs*22) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000237172 |
| Start | 75315194:75315194(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.638delA |
| AA Mutation | p.Lys213SerfsTer24(p.K213Sfs*24) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 27 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000237172 |
| Start | 75314277:75314277(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1555delA |
| AA Mutation | p.Ile519Ter(p.I519*) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 28 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000237172 |
| Start | 75414792:75414792(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.181delA |
| AA Mutation | p.Thr61HisfsTer26(p.T61Hfs*26) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 29 |
| Mutation Consequence | inframe_deletion |
| Transcription ID | ENST00000237172 |
| Start | 75312504:75312506(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs776863722 |
| CDS Mutation | c.3326_3328delTTC |
| AA Mutation | p.Leu1109del(p.L1109del) |
| Mutation Classification | In_Frame_Del |
| Feature Type | Transcript |
| ID | 30 |
| Mutation Consequence | inframe_deletion |
| Transcription ID | ENST00000237172 |
| Start | 75353655:75353660(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.508_513delTTGCTG |
| AA Mutation | p.Leu170_Leu171del(p.L170_L171del) |
| Mutation Classification | In_Frame_Del |
| Feature Type | Transcript |