Primary Site >> Stomach Cancer
Gene >> FBXL7
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000504595 |
| Start | 15936834:15936834(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1124G>A |
| AA Mutation | p.Cys375Tyr(p.C375Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000504595 |
| Start | 15936795:15936795(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1085G>A |
| AA Mutation | p.Arg362Gln(p.R362Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000504595 |
| Start | 15928342:15928342(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.580A>G |
| AA Mutation | p.Ser194Gly(p.S194G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000504595 |
| Start | 15936738:15936738(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1028G>A |
| AA Mutation | p.Arg343Gln(p.R343Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000504595 |
| Start | 15928333:15928333(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.571G>A |
| AA Mutation | p.Val191Ile(p.V191I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000504595 |
| Start | 15616006:15616006(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.61T>C |
| AA Mutation | p.Ser21Pro(p.S21P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000504595 |
| Start | 15928013:15928013(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.251C>T |
| AA Mutation | p.Thr84Met(p.T84M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000504595 |
| Start | 15937148:15937148(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs576303242 |
| CDS Mutation | c.1438C>T |
| AA Mutation | p.Arg480Cys(p.R480C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000504595 |
| Start | 15928217:15928217(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs548322966 |
| CDS Mutation | c.455G>A |
| AA Mutation | p.Arg152Gln(p.R152Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000504595 |
| Start | 15937017:15937017(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1307A>G |
| AA Mutation | p.Lys436Arg(p.K436R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000504595 |
| Start | 15616034:15616034(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs376437263 |
| CDS Mutation | c.89C>T |
| AA Mutation | p.Thr30Met(p.T30M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000504595 |
| Start | 15936483:15936483(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs189208873 |
| CDS Mutation | c.773G>A |
| AA Mutation | p.Arg258Gln(p.R258Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000504595 |
| Start | 15937154:15937154(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1444G>A |
| AA Mutation | p.Val482Ile(p.V482I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000504595 |
| Start | 15928312:15928312(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.550G>A |
| AA Mutation | p.Val184Met(p.V184M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000504595 |
| Start | 15936647:15936647(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.937G>A |
| AA Mutation | p.Asp313Asn(p.D313N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000504595 |
| Start | 15936560:15936560(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.850G>A |
| AA Mutation | p.Val284Met(p.V284M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000504595 |
| Start | 15936815:15936815(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1105C>T |
| AA Mutation | p.Arg369Cys(p.R369C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000504595 |
| Start | 15928021:15928021(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.259A>G |
| AA Mutation | p.Met87Val(p.M87V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000504595 |
| Start | 15928268:15928268(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.506C>T |
| AA Mutation | p.Ala169Val(p.A169V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000504595 |
| Start | 15936642:15936642(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.932T>C |
| AA Mutation | p.Leu311Pro(p.L311P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000504595 |
| Start | 15936700:15936700(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.990C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000504595 |
| Start | 15936856:15936856(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs746695934 |
| CDS Mutation | c.1146C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000504595 |
| Start | 15936712:15936712(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs559305174 |
| CDS Mutation | c.1002C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000504595 |
| Start | 15936724:15936724(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs759822107 |
| CDS Mutation | c.1014C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000504595 |
| Start | 15936958:15936958(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1248C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000504595 |
| Start | 15936802:15936802(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1092C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 27 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000504595 |
| Start | 15937138:15937138(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1428C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 28 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000504595 |
| Start | 15928005:15928005(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs770680382 |
| CDS Mutation | c.243C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 29 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000504595 |
| Start | 15936595:15936595(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs773852697 |
| CDS Mutation | c.885G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |