SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs718089 | snp | C/T | 0.494442 | 0.0524218 | intron-variant, upstream-variant-2KB | FBXW7, MIR3140 | GRCh38.p7 | 4:152491242 | TTCTATTACTGCTTA[C/T]GTTGTAAGGTCAGTA | 55294 |
rs900977 | snp | C/G | 0.0267878 | 0.112589 | intron-variant | FBXW7 | GRCh38.p7 | 4:152460170 | TAAGTTTTTTAGAAA[C/G]CTATTATACATTACT | 55294 |
rs938633 | snp | C/T | 0 | 0 | intron-variant | FBXW7 | GRCh38.p7 | 4:152402661 | ACATATTTCTCATCT[C/T]CATTATGGGGTTAAA | 55294 |
rs952794 | snp | G/T | 0 | 0 | intron-variant | FBXW7 | GRCh38.p7 | 4:152392203 | ggcctctccctctta[G/T]tgaaaggagtctcag | 55294 |
rs964475 | snp | C/T | 0.4944 | 0.0526182 | intron-variant | FBXW7 | GRCh38.p7 | 4:152431643 | GTCCCATAATTTTTA[C/T]TGAACAATACTTACC | 55294 |
rs972185 | snp | G/T | 0 | 0 | intron-variant | FBXW7 | GRCh38.p7 | 4:152508678 | TTTAACTTCCTTGCt[G/T]ttttttttttctttt | 55294 |
rs1023962 | snp | G/T | 0.495291 | 0.0482933 | intron-variant | FBXW7 | GRCh38.p7 | 4:152530204 | TAAGTGATTTGTTAA[G/T]ATACACTAGTACTTG | 55294 |
rs1351903 | snp | A/G | 0.493523 | 0.0565391 | utr-variant-5-prime, upstream-variant-2KB, intron-variant | FBXW7, DKFZP434I0714, MIR4453 | GRCh38.p7 | 4:152534950 | ACTCACACTTTTAGA[A/G]AAGAGCCGCGGCGCC | 55294 |
rs1356300 | snp | G/T | 0.492966 | 0.0588865 | intron-variant | FBXW7 | GRCh38.p7 | 4:152464317 | TACTATTTTTCTTCC[G/T]CTTAATGCTCCATGC | 55294 |
rs1400407 | snp | C/T | 0 | 0 | intron-variant | FBXW7 | GRCh38.p7 | 4:152485269 | AATTTGAAACTTTTT[C/T]TAATAGGAAGGTTAA | 55294 |
rs1400408 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | FBXW7 | GRCh38.p7 | 4:152421744 | CTGTAGGGTTATTAA[C/T]TGGCAAAATTTCAAT | 55294 |
rs1484879 | snp | A/G | 0.495095 | 0.0492773 | intron-variant, upstream-variant-2KB | FBXW7, DKFZP434I0714, MIR4453 | GRCh38.p7 | 4:152534476 | ATGAACCTCTCTCAA[A/G]ACAGGTTTGTTGTTG | 55294 |
rs1516819 | snp | A/C | 0.494896 | 0.0502606 | intron-variant | FBXW7 | GRCh38.p7 | 4:152512299 | ACACAGTAAACAACA[A/C]CAAGATGGAAAATAA | 55294 |
rs1516820 | snp | A/G | 0.494013 | 0.0543839 | intron-variant | FBXW7 | GRCh38.p7 | 4:152459649 | tggtttcaagcatcc[A/G]ctggggggtctggaa | 55294 |
rs1516822 | snp | C/T | 0.48818 | 0.0759629 | intron-variant | FBXW7 | GRCh38.p7 | 4:152409149 | GGATGATGGGTAAAA[C/T]TCAGTCTAGCTGTCC | 55294 |
rs1516823 | snp | C/T | 0.204189 | 0.245767 | intron-variant | FBXW7 | GRCh38.p7 | 4:152435720 | gactgcagtttactg[C/T]acttcacaaatagta | 55294 |
rs1533467 | snp | A/G | 0 | 0 | intron-variant | FBXW7 | GRCh38.p7 | 4:152464223 | AGGTTGTTATAGTCC[A/G]TTCTAGGTGTCTCCA | 55294 |
rs1607107 | snp | C/T | 0.019266 | 0.0962384 | intron-variant | FBXW7 | GRCh38.p7 | 4:152436495 | GCTGCAGCAAGTTAC[C/T]TAAAAGGTCTAGCTA | 55294 |
rs1607108 | snp | C/T | 0.00583085 | 0.0536789 | intron-variant | FBXW7 | GRCh38.p7 | 4:152436791 | ATGGAATAACAGAGC[C/T]TAGATGGCAGCACAT | 55294 |
rs1850328 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | FBXW7 | GRCh38.p7 | 4:152443081 | CAGCTTGACCAACAC[A/G]GAGAAGCCCTGTCTC | 55294 |
rs1878342 | snp | A/C | 0.0271762 | 0.113356 | intron-variant | FBXW7 | GRCh38.p7 | 4:152416860 | TGGCTAAATTTAATC[A/C]CTGTGTGATACGCCA | 55294 |
rs1961679 | snp | C/T | 0.492582 | 0.0604491 | intron-variant | FBXW7 | GRCh38.p7 | 4:152500182 | TGACCATTCACTTAC[C/T]TCCCCTATTCCCTCT | 55294 |
rs1967047 | snp | G/T | | | intron-variant | FBXW7 | GRCh38.p7 | 4:152463180 | taatcccagctactc[G/T]ggaggctgacgcatg | 55294 |
rs1994242 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | FBXW7 | GRCh38.p7 | 4:152524817 | AAAGTTTAGTATTTA[C/T]CCGCAGGGGGGAAAA | 55294 |
rs2035535 | snp | A/T | 0.487113 | 0.0792303 | intron-variant | FBXW7 | GRCh38.p7 | 4:152423870 | AGGAGTCACTAGAGG[A/T]GGTTCTGGAATAGAA | 55294 |
rs2037210 | snp | C/G | | | intron-variant | FBXW7 | GRCh38.p7 | 4:152424416 | TTAAACAGAAATATA[C/G]CTAGAGACACTAAAC | 55294 |
rs2054758 | snp | G/T | 0.0475351 | 0.146656 | intron-variant | FBXW7 | GRCh38.p7 | 4:152484060 | GAATAGAGTCTACAT[G/T]CAACACTATTTGGTT | 55294 |
rs2176326 | snp | C/T | 0 | 0 | intron-variant | FBXW7 | GRCh38.p7 | 4:152397851 | AGAAAAAAATTATTT[C/T]TCCAAAAAAGCTACT | 55294 |
rs2176327 | snp | A/C | 0 | 0 | intron-variant | FBXW7 | GRCh38.p7 | 4:152397805 | TCATCTTGTATTAGC[A/C]CAGACAGTAATATTG | 55294 |
rs2176328 | snp | A/C | | | intron-variant | FBXW7 | GRCh38.p7 | 4:152397777 | TTGTGGGGTATAACC[A/C]CCTAATCATCGTGGA | 55294 |
rs2203644 | snp | A/G | 0.496105 | 0.0439572 | intron-variant, upstream-variant-2KB | FBXW7 | GRCh38.p7 | 4:152354549 | ATTTCAGTTGAAGCC[A/G]AAGTATATACTATTA | 55294 |
rs2255137 | snp | A/G | 0.44858 | 0.151875 | intron-variant | FBXW7 | GRCh38.p7 | 4:152388386 | AGGCATGTACATGCA[A/G]TGCTTTTATTTTGCA | 55294 |
rs2292743 | snp | A/T | 0.499997 | 0.00119808 | intron-variant | FBXW7 | GRCh38.p7 | 4:152411948 | ATGTTATATGTCTAC[A/T]TTCTAAATATCATTA | 55294 |
rs2406375 | snp | A/G | 0.49423 | 0.0534032 | intron-variant | FBXW7 | GRCh38.p7 | 4:152446105 | AGGATATTTTTTAGT[A/G]AACACGTTTTAAGAA | 55294 |
rs2406600 | snp | C/T | 0.492037 | 0.0625946 | intron-variant | FBXW7 | GRCh38.p7 | 4:152389254 | tgctggatcaaatga[C/T]agttctattattagt | 55294 |
rs2459506 | snp | C/T | | | intron-variant | FBXW7 | GRCh38.p7 | 4:152340489 | cgggttaaccccttt[C/T]tcctacataagcctc | 55294 |
rs2465522 | snp | G/T | | | intron-variant | FBXW7 | GRCh38.p7 | 4:152340498 | gtaggagaatggcgt[G/T]aacccgggaggagct | 55294 |
rs2628570 | snp | A/C | 0.495483 | 0.0473088 | intron-variant | FBXW7 | GRCh38.p7 | 4:152452528 | GTATTGAACACTATT[A/C]TGAGACACAGCTGAT | 55294 |
rs2628571 | snp | A/T | | | intron-variant | FBXW7 | GRCh38.p7 | 4:152437381 | cagactccatctcaa[A/T]aaaaaaaaaaattca | 55294 |
rs2676329 | snp | A/G | 0.490398 | 0.0686206 | intron-variant, upstream-variant-2KB | FBXW7 | GRCh38.p7 | 4:152354243 | TAATTTAAGAGCCAG[A/G]TAGGAGATTTTTTTT | 55294 |
rs2676330 | snp | A/G | 0.495963 | 0.0447464 | intron-variant | FBXW7 | GRCh38.p7 | 4:152344355 | GAAATCTGTAGCAAC[A/G]AAAGGTCAACTGGAC | 55294 |
rs2676331 | snp | G/T | | | intron-variant | FBXW7 | GRCh38.p7 | 4:152340536 | caacctggagggcag[G/T]ggtacaattttggtt | 55294 |
rs2676332 | snp | C/T | 0.0803491 | 0.183626 | intron-variant | FBXW7 | GRCh38.p7 | 4:152446983 | GTATTTGTAATCTTT[C/T]ATTATTCAACAGGTA | 55294 |
rs2676333 | snp | G/T | 0.0437281 | 0.141251 | intron-variant | FBXW7 | GRCh38.p7 | 4:152408631 | CTATAGGGTAGCTCT[G/T]ATCACTTCAAATGGG | 55294 |
rs2676334 | snp | A/C | 0.490184 | 0.0693654 | intron-variant | FBXW7 | GRCh38.p7 | 4:152419496 | ctaggataaggtaaa[A/C]acacacacacacaca | 55294 |
rs2676336 | snp | C/T | 0.079617 | 0.182947 | intron-variant | FBXW7 | GRCh38.p7 | 4:152431976 | CTCATTGTGATTGTG[C/T]AGAGGCTCCCTGTAA | 55294 |
rs2676337 | snp | C/T | 0.494733 | 0.0510469 | intron-variant | FBXW7 | GRCh38.p7 | 4:152437154 | taccattaagaatat[C/T]tgtgtttcacagaag | 55294 |
rs2676338 | snp | C/T | | | intron-variant | FBXW7 | GRCh38.p7 | 4:152397946 | GCTTTTAGAAAATTT[C/T]TCAAGTATTTGAACA | 55294 |
rs2676339 | snp | C/T | 0 | 0 | intron-variant | FBXW7 | GRCh38.p7 | 4:152397937 | AAATTTTTCAAGTAT[C/T]TGAACATATACGTGT | 55294 |
rs2676341 | snp | C/T | 0 | 0 | intron-variant | FBXW7 | GRCh38.p7 | 4:152397827 | AGCTACTTCCCTTGT[C/T]TAAATGTCATCTTGT | 55294 |
rs2676343 | snp | A/G | 0.499035 | 0.0219437 | intron-variant | FBXW7 | GRCh38.p7 | 4:152389475 | GAAGAATCACCTCCA[A/G]TTCCATCCATGTTGC | 55294 |
rs2676344 | snp | C/T | 0.495782 | 0.0457324 | intron-variant | FBXW7 | GRCh38.p7 | 4:152384729 | CCATTTTCAATCATT[C/T]ACTTTTTTGTTTAAA | 55294 |
rs2676345 | snp | A/G | 0.0803491 | 0.183626 | intron-variant | FBXW7 | GRCh38.p7 | 4:152374060 | ACTTGGAAAATATAA[A/G]CATTTCCAGATCCTT | 55294 |
rs2714798 | snp | G/T | 0.325327 | 0.238382 | intron-variant | FBXW7 | GRCh38.p7 | 4:152416110 | TGATGAAAAACAAAA[G/T]TCCCTTTTCCTTATA | 55294 |
rs2714799 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | FBXW7 | GRCh38.p7 | 4:152407797 | GGATCATTTGGGCCC[A/T]GGAGGTTGAGGCTGC | 55294 |
rs2714801 | snp | A/G | 0 | 0 | intron-variant | FBXW7 | GRCh38.p7 | 4:152340630 | AGACGAGTAGCAATA[A/G]AAAATGAGACTGTTT | 55294 |
rs2714802 | snp | A/G | 0 | 0 | intron-variant | FBXW7 | GRCh38.p7 | 4:152340638 | AGCAATAGAAAATGA[A/G]ACTGTTTCCACTGAC | 55294 |
rs2714803 | snp | A/G | 0.0803491 | 0.183626 | intron-variant | FBXW7 | GRCh38.p7 | 4:152346816 | CAGAATGATTTCAAA[A/G]TTCATCCACAGTATA | 55294 |
rs2714804 | snp | A/G | 0.193028 | 0.243422 | intron-variant | FBXW7 | GRCh38.p7 | 4:152349812 | ATTTTTGTTCACAAG[A/G]TAATTTCTGCTTGTG | 55294 |
rs2714805 | snp | C/T | 0.492775 | 0.059668 | intron-variant | FBXW7 | GRCh38.p7 | 4:152373723 | TGCCTCCTCATACTC[C/T]GACAGTACTTTGTAC | 55294 |
rs2859690 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXW7 | GRCh38.p7 | 4:152340680 | AACTGTCCTATCGTT[A/T]AAAATCACATCTCTT | 55294 |
rs2897393 | snp | A/G | 0 | 0 | intron-variant | FBXW7 | GRCh38.p7 | 4:152520672 | GTTGGAAAGATGAAT[A/G]TGTAGTATCATTTTT | 55294 |
rs3047829 | in-del | -/TTC | 0.494733 | 0.0510469 | intron-variant | FBXW7 | GRCh38.p7 | 4:152485511 | TTCATATTCCTCTTC[-/TTC]CATAATGAAGATCCA | 55294 |
rs3047865 | in-del | -/TG | | | intron-variant | FBXW7 | GRCh38.p7 | 4:152418127 | gtgtgtgtgtgtgtg[-/TG]gtAAGAGCTGTTCTT | 55294 |
rs3083257 | in-del | -/TGTC | | | intron-variant | FBXW7 | GRCh38.p7 | 4:152510092 | TGCAGTGAACATCTT[-/TGTC]TGTGTGCTACCCAGT | 55294 |
rs3733263 | snp | A/G | 0.111928 | 0.208413 | upstream-variant-2KB, nc-transcript-variant | FBXW7, DKFZP434I0714, MIR4453 | GRCh38.p7 | 4:152536305 | TGCGCCTCGGGCCGC[A/G]GGACTCGCAGCCGCC | 55294 |
rs3841114 | in-del | -/T | 0 | 0 | utr-variant-3-prime | FBXW7 | GRCh38.p7 | 4:152322325 | TTTTTTTTTTTTTTT[-/T]GCCAACCATTGCCAA | 55294 |
rs4146039 | snp | C/G | 0.493477 | 0.0567349 | intron-variant | FBXW7 | GRCh38.p7 | 4:152449955 | AGCACCCTTTTTGGG[C/G]AAGATAGTCTAAAAC | 55294 |
rs4315757 | snp | C/T | 0.0799831 | 0.183287 | intron-variant | FBXW7 | GRCh38.p7 | 4:152326991 | CATTTGGTTCAACAT[C/T]AGCGCTATACTCTTC | 55294 |
rs4399968 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | FBXW7 | GRCh38.p7 | 4:152322172 | CTACTTCTAGCACCA[C/G]CATCAAGAATTAAAT | 55294 |
rs4419460 | snp | C/T | 0.0803491 | 0.183626 | intron-variant | FBXW7 | GRCh38.p7 | 4:152327994 | TTTCAAACAGGAAGC[C/T]GACAACACTAGCAAA | 55294 |
rs4443256 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | FBXW7 | GRCh38.p7 | 4:152403635 | caccacgcattagac[C/T]ctcggaaggagcata | 55294 |
rs4558853 | snp | C/T | 0.0143671 | 0.0835292 | intron-variant | FBXW7 | GRCh38.p7 | 4:152526439 | GAAGAAAAGGTATTT[C/T]TGAAAACCAATCTTG | 55294 |
rs4696318 | snp | A/G | 0.492435 | 0.0610346 | intron-variant | FBXW7 | GRCh38.p7 | 4:152381454 | CATAAACCTATGTTA[A/G]ATCTAAAAATATATC | 55294 |
rs4696319 | snp | C/T | 0.0633504 | 0.166319 | intron-variant | FBXW7 | GRCh38.p7 | 4:152381679 | CCACACAATAGCATG[C/T]TATTTTTATTTTATA | 55294 |
rs4696321 | snp | C/T | 0.493925 | 0.054776 | intron-variant | FBXW7 | GRCh38.p7 | 4:152421493 | gcttgaggtcaggag[C/T]tcaagaacagcctga | 55294 |
rs4696322 | snp | C/T | 0.207253 | 0.246318 | intron-variant | FBXW7 | GRCh38.p7 | 4:152438452 | GGAGGCCAAGCCAGG[C/T]GGATCACTTGAGGTC | 55294 |
rs4696323 | snp | G/T | 0.00865784 | 0.0652224 | upstream-variant-2KB, nc-transcript-variant, downstream-variant-500B | FBXW7, DKFZP434I0714, MIR4453 | GRCh38.p7 | 4:152536889 | GAGTCACAACCTGAG[G/T]CTTTAGTGGAAAAGG | 55294 |
rs4986777 | snp | A/C/T | | | intron-variant | FBXW7 | GRCh38.p7 | 4:152530070 | CAAAAAAAAAAAAAA[A/C/T]ACACACACACACACA | 55294 |
rs5019288 | snp | A/C | | | intron-variant | FBXW7 | GRCh38.p7 | 4:152530072 | aaaaaaaaaaaaaTa[A/C]acacacacacacaca | 55294 |
rs5863003 | in-del | -/A | 0.495745 | 0.0459295 | intron-variant | FBXW7 | GRCh38.p7 | 4:152349314 | AGACCAAAAAAAAAA[-/A]GCTCTAAGATACTTC | 55294 |
rs5863005 | in-del | -/T | 0.121022 | 0.21416 | intron-variant | FBXW7 | GRCh38.p7 | 4:152410533 | ACACATTTTAGAAAG[-/T]TAAGGTTTTACAAGC | 55294 |
rs5863008 | in-del | -/A | | | intron-variant | FBXW7 | GRCh38.p7 | 4:152446713 | CTAACTTTTATAAAA[-/A]GTAGTCAACACTCTG | 55294 |
rs5863009 | in-del | -/A | | | intron-variant | FBXW7 | GRCh38.p7 | 4:152484978 | AAAAAAAAAAAAAAA[-/A]GTATAAAGCCCAATT | 55294 |
rs6535846 | snp | C/T | 0.0788843 | 0.182262 | intron-variant | FBXW7 | GRCh38.p7 | 4:152334981 | AGTAGAGCACAAATA[C/T]GCTGTCAACAAGGTT | 55294 |
rs6535847 | snp | C/T | 0.496382 | 0.0423778 | intron-variant, upstream-variant-2KB | FBXW7, DEAR | GRCh38.p7 | 4:152335693 | TTTCTCTATAACCTA[C/T]ATAAAAGACAACCAC | 55294 |
rs6535848 | snp | C/T | 0.210909 | 0.246925 | intron-variant | FBXW7 | GRCh38.p7 | 4:152378721 | AACATACACTTATTA[C/T]GCCGGGCATGGTGGT | 55294 |
rs6535849 | snp | A/G | 0.493432 | 0.0569306 | intron-variant | FBXW7 | GRCh38.p7 | 4:152378963 | GTAAGCCAAGATGGC[A/G]CCACTACACTCCAGC | 55294 |
rs6535851 | snp | C/T | 0.495634 | 0.0465208 | intron-variant | FBXW7 | GRCh38.p7 | 4:152504297 | ttttcataacacaaa[C/T]caataaaaaagattt | 55294 |
rs6535852 | snp | C/T | 0.49607 | 0.0441545 | intron-variant | FBXW7 | GRCh38.p7 | 4:152504734 | aagatcaattacttc[C/T]ggtaaaaagttagtg | 55294 |
rs6816935 | snp | C/T | 0.00246609 | 0.035028 | missense, synonymous-codon, intron-variant | FBXW7 | GRCh38.p7 | 4:152411461 | GGTCCATCTCCTCCT[C/T]CTCCTCATCCTCCTC | 55294 |
rs6816962 | snp | G/T | 0.492582 | 0.0604491 | intron-variant | FBXW7 | GRCh38.p7 | 4:152529208 | CATCCTTAGGCTTGG[G/T]ACAATGATAAAATTA | 55294 |
rs6817854 | snp | A/G | 0.0799831 | 0.183287 | upstream-variant-2KB, nc-transcript-variant | FBXW7, DKFZP434I0714 | GRCh38.p7 | 4:152537152 | CCTGTTTCAGGTCTG[A/G]CTCAAAGGTTATTTT | 55294 |
rs6820601 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | FBXW7 | GRCh38.p7 | 4:152454261 | tctaagccccccccc[C/G]ctttttttttttttt | 55294 |
rs6826158 | snp | C/T | 0 | 0 | intron-variant | FBXW7 | GRCh38.p7 | 4:152342754 | ACTTAATGCCAAAAT[C/T]TGACTCAAAGAACAT | 55294 |
rs6826200 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | FBXW7 | GRCh38.p7 | 4:152407771 | ggtcttgctctgtgg[C/G]ccagatcactgcagc | 55294 |
rs6835854 | snp | C/G | 0 | 0 | intron-variant | FBXW7 | GRCh38.p7 | 4:152339075 | ATCTACAATGAACTT[C/G]TTCTCTTCTTTCTTA | 55294 |
rs6842544 | snp | C/T | 0.00362381 | 0.0424119 | FBXW7 | 4 | allele_origin=T(germline)/C(germline) | 4:152411407 | TATGTTCATCTTCTC[C/T]GCTACTATCATCAGA | 55294 |
rs6843927 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | FBXW7 | GRCh38.p7 | 4:152516113 | cttaatttcagccta[C/G]tgagaacctgaggaa | 55294 |
rs6852336 | snp | C/G | 0.495596 | 0.0467178 | intron-variant | FBXW7 | GRCh38.p7 | 4:152439603 | GTCCACGGTGGCTCA[C/G]GCCTGTAATCCCAGC | 55294 |