SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs201437404 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101655651 | CAGGTTTCTCTAGGA[C/T]AGCTAAAGCTGCAGC | 6468 |
rs201467007 | in-del | -/A | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101634691 | CTGAATACACATTTG[-/A]AAAAAAAAAATTAGA | 6468 |
rs201521707 | in-del | -/A | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101613148 | CAGCCTGCTCCCCCC[-/A]CCCTCACCCCACCCG | 6468 |
rs201585955 | snp | A/G | 0.000543454 | 0.0164752 | intron-variant | FBXW4 | GRCh38.p7 | 10:101612494 | TGGGAAGGGAAGGAC[A/G]GAGTGAGAGGCTGCT | 6468 |
rs201649310 | snp | A/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101642397 | CTCTATTTTTTTTTT[A/T]AATTAAAAAAAAAAC | 6468 |
rs201658274 | snp | A/C | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101677794 | CCCTCTCTAAAAAAA[A/C]AAAAAGAGAAAAGAA | 6468 |
rs201711223 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101681245 | ATACAAAAATTAGCC[A/G]GGCGTTGTAGTGGGC | 6468 |
rs201774923 | snp | A/C | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101636410 | CGGAAAAAAAAAAAA[A/C]AAAAAAGAATTGCAA | 6468 |
rs202020612 | in-del | -/A | 0.0337553 | 0.125452 | intron-variant | FBXW4 | GRCh38.p7 | 10:101674774 | TCCCTCTGCAATCTG[-/A]CAGGAGGAAGAAAGG | 6468 |
rs202042320 | in-del | -/GTACC | 0.0146672 | 0.084371 | intron-variant | FBXW4 | GRCh38.p7 | 10:101641740 | AGACATTTGAAGTTG[-/GTACC]TAAATCAGAAATTAG | 6468 |
rs202127189 | in-del | -/A | 0.357451 | 0.225731 | intron-variant | FBXW4 | GRCh38.p7 | 10:101624271 | CAAAATTAGAAAGTT[-/A]AAAAAAAAAAAAAAA | 6468 |
rs367580076 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101650556 | GGGGTAGAACTAACC[A/G]CCCCCCTCAAGGGGT | 6468 |
rs367635620 | snp | A/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101679907 | TTCCTCCCTTCTGAA[A/T]CTCCAATGTCCATTA | 6468 |
rs367644540 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101653643 | GCTTTCCTCTGATTT[C/T]CTGTCAATAACCCCA | 6468 |
rs367659610 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | FBXW4 | GRCh38.p7 | 10:101640977 | CTGGGATTACTGGCA[C/T]CCGCCACCACACCCA | 6468 |
rs367664173 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101654080 | GAGCCGAGATTGCAC[C/T]ACTGCACTCCAGACC | 6468 |
rs367690512 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101634950 | AACAAGCTGAAAGGA[A/G]TTACCATATACAGCA | 6468 |
rs367757549 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101667223 | GTGACAGAGCGAGAC[C/T]CCGTCTCAAAAAAAA | 6468 |
rs367863289 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | FBXW4 | GRCh38.p7 | 10:101624731 | AAGCCAGCATGGGCT[C/T]ATGAATCTCTTACCT | 6468 |
rs368015804 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101650526 | GTTTAACTCACTTCA[A/G]GCTGGCAGCCCTATG | 6468 |
rs368083209 | snp | G/T | | | upstream-variant-2KB | FBXW4 | GRCh38.p7 | 10:101696016 | TATTTTGGATACGCT[G/T]TATTGGGCTAAATAC | 6468 |
rs368115198 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101618746 | GCTTAGGGCTGTGAC[C/T]GTGGCTGGACCTACT | 6468 |
rs368117036 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101655913 | TTGGACCCAGGGCAA[A/G]AATCAAGCTAATTTC | 6468 |
rs368185192 | snp | A/G | 1.66004e-05 | 0.00288096 | synonymous-codon, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101611375 | ACGCAGGCAGTACAC[A/G]GGGCTGCTGAGGGGA | 6468 |
rs368202747 | snp | C/G | 1.68829e-05 | 0.00290537 | intron-variant | FBXW4 | GRCh38.p7 | 10:101673064 | TAGGAGAGAAATAAG[C/G]AGCCGACCCCCAAGA | 6468 |
rs368224962 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101677356 | AAAAAGGAAAGAAGT[A/G]CTGATACACAACATA | 6468 |
rs368247049 | in-del | -/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101618889 | TCAAATGCCCCTTGG[-/G]CAGAAAAAAAAAACC | 6468 |
rs368262003 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | FBXW4 | GRCh38.p7 | 10:101641392 | CATCCACAATCAAAA[A/C]CAATTGACTGTGATC | 6468 |
rs368317323 | snp | C/G | 4.94295e-05 | 0.00497115 | missense, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101673623 | GCCAGGATGAAATTA[C/G]CCTGGGATATGTACA | 6468 |
rs368317611 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101638367 | AGAACAAATGTATAA[C/T]GTGAGCCTAAAACAA | 6468 |
rs368343324 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101623913 | ACATAAGAAGTTGCC[A/G]GGAATCAGGGACAAT | 6468 |
rs368388670 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101682822 | ACTTGGCTGTAGTCC[C/T]TCAAATTTAGACTTT | 6468 |
rs368440221 | snp | A/C | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101657639 | AGCGAGACTCTGTCT[A/C]AAAAAAAAAAAAAAA | 6468 |
rs368487891 | multinucleotide-polymorphism | AA/GC | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101655656 | TTCTCTAGGACAGCT[AA/GC]AGCTGCAGCTGCAAC | 6468 |
rs368491758 | snp | A/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101631077 | TTTTTTTTATCAAAC[A/T]AAAGCCGAATAAGAA | 6468 |
rs368764209 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101650489 | ACAATCTGTGCTCCT[A/G]CCAGACCCAGTCACA | 6468 |
rs368769258 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | FBXW4 | GRCh38.p7 | 10:101669977 | AGCCAGGATGGTCTC[A/G]ATCTCCTGACCTCAT | 6468 |
rs368779727 | snp | A/G | 1.67192e-05 | 0.00289125 | synonymous-codon, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101612378 | GCGAACATAGGTGTC[A/G]TAGCCACAGGACAGC | 6468 |
rs368922465 | snp | C/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101658374 | ACATGGTGAAACCCC[C/G]TCTCTACTAAAAATA | 6468 |
rs368925861 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101640932 | ACCTCCCAGGTTCAA[A/G]CAATTCTTCTGCCTC | 6468 |
rs368965299 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | FBXW4 | GRCh38.p7 | 10:101681604 | CGCCTGTAGTCCCAG[A/C]TACTCGGAAGGCTGA | 6468 |
rs369006293 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101620193 | ACCCCAAGTCCTGCC[A/G]GCAATGCTGCTCCAC | 6468 |
rs369066487 | in-del | -/TTAAGAGAT | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101641167 | CATAATGCCAGGCAT[-/TTAAGAGAT]AGATAATTTAAATAT | 6468 |
rs369081403 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101628062 | GGCTCCTGTGCTAGG[C/T]GTGTCAAAGGCTCTC | 6468 |
rs369143598 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101692526 | TTTGGGAGGCCGAGG[G/T]GGGCAGATAACCTGA | 6468 |
rs369153808 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101682943 | GTCTAACCATCTTGG[A/G]TGGTTACAGTTTCCC | 6468 |
rs369168511 | in-del | -/C | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101620537 | TGGTGCCCAGGGCAA[-/C]CCCTGCCACAAGCAG | 6468 |
rs369336513 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101683748 | ATTTCCCTCTCTGTC[C/T]CATCTCACAGCTTGA | 6468 |
rs369342554 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101618095 | AGCCTGTGTGCAGGA[C/T]ACGGCTTCCTTCTCC | 6468 |
rs369398066 | in-del | -/AG | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101618406 | TTTCATTAGGCACAG[-/AG]GGGGTATTCTGGGCA | 6468 |
rs369413233 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101653877 | ACTGTAATCCCAGCA[C/T]TTTAGGAGGCCAAGG | 6468 |
rs369417049 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FBXW4 | GRCh38.p7 | 10:101657803 | ATTCATTGATCTGCT[A/G]ATGCATGTATTCTTT | 6468 |
rs369425688 | snp | G/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101639973 | TAAATGTGTCCTGAG[G/T]AATATAGAGCCTCTG | 6468 |
rs369462709 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101630333 | CTGCAAGTGGGCTCC[C/T]GAACCGCCCTGCTTG | 6468 |
rs369489484 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101688895 | GGAGCCTGGTCTCAA[C/T]AAGAATCTGCCTAAA | 6468 |
rs369600539 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101643525 | GCAGGCATATGCACG[C/T]TTTGCATTACATCTC | 6468 |
rs369608923 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101621192 | CAGCAGGTTCACCTC[C/T]GCCTCCACTAGTCAC | 6468 |
rs369639920 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101653014 | ACCCCACGTGTGAGT[C/T]CCAGGCAACCATTCC | 6468 |
rs369640712 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101626849 | TAAATTAGCATCAAG[G/T]TAAATCAATAGAGAG | 6468 |
rs369647099 | snp | A/G | 1.75536e-05 | 0.00296251 | intron-variant | FBXW4 | GRCh38.p7 | 10:101611440 | ACAGGAAGTGGTAAG[A/G]GCTTTCCAAGTGGGA | 6468 |
rs369648383 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101633770 | ATATATCAGCAATAA[C/T]AAACTGTTATTATAT | 6468 |
rs369649315 | snp | G/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101641144 | CCAACCCTTCCATTT[G/T]CAACAACCATAATGC | 6468 |
rs369800083 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101663668 | GTCTGCCCTTCTGTG[C/T]TACTCTTGGGAAGTT | 6468 |
rs370127073 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101647648 | CAAAAAGTCATTTCA[C/T]TGGAAGCTTCCTTTC | 6468 |
rs370172283 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101670054 | GCCACCGCGCCCGGC[C/T]GGGAGTGGACATTTA | 6468 |
rs370266402 | snp | A/C | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101641631 | TGTAAGATTTTTTCT[A/C]AAAAAAAAACAAAAC | 6468 |
rs370310236 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101637585 | TGGTGGTGCATGCCT[A/G]TAATCCCATCTACTT | 6468 |
rs370390474 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101672164 | CATAACAAGACACTA[C/T]TGGGCCTCCTGCACC | 6468 |
rs370392619 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101637874 | CTGCAAAGTCGACCC[C/T]GTAATCACTATTTTA | 6468 |
rs370436773 | snp | A/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101693630 | AAAAAATGGGTGGAA[A/T]AGGGGGCAATCTGAA | 6468 |
rs370508180 | snp | A/C | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101675436 | ACTGCTTGAAACTAG[A/C]CCCAAAAGGCAAATG | 6468 |
rs370562580 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101622523 | ACGAGGTCAGGAGAT[C/T]GAGACCATCCTGGCT | 6468 |
rs370573808 | snp | C/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101631034 | ACCAAAGCTGCAAGA[C/G]CAGGCAGGGGAAGAT | 6468 |
rs370753810 | snp | A/C | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101664429 | ACCAGGAGTACCTGC[A/C]CTAGGGCCAGTACAC | 6468 |
rs370764431 | snp | A/G | 1.65116e-05 | 0.00287324 | synonymous-codon, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101611724 | ATCTGTCTGCAGGCA[A/G]TACAGGGTGCTGTCG | 6468 |
rs370804592 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | FBXW4 | GRCh38.p7 | 10:101612313 | GGGCCCCCACCACCT[A/G]TCCTCCCTGCCCAGC | 6468 |
rs370920435 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101653440 | AAATTTCCCCTCCAG[C/T]GAGCCAGACTTGTCC | 6468 |
rs371025846 | snp | C/T | 1.66527e-05 | 0.00288549 | missense, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101612414 | GAAAGGGGACTCATA[C/T]ATGACATCCAGCACC | 6468 |
rs371115156 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101694294 | GGTGCGACACGACCC[C/T]GGGCCGACCAGGCCG | 6468 |
rs371128064 | snp | A/C | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101672859 | CTCAGGGATCTATCC[A/C]CCCCCTCCCTATAGA | 6468 |
rs371197433 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101645411 | TTCTGTCTTCCCATC[C/T]TCCTGTGCCCCTGTG | 6468 |
rs371243446 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101675046 | TTTCTTCCCCAGACT[C/T]GTACAAGTGTCATGG | 6468 |
rs371350391 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101691397 | CAATCCAGAAAACCC[A/G]AGCAGTGACCCTGCT | 6468 |
rs371351509 | snp | G/T | 0.00318978 | 0.0398085 | upstream-variant-2KB | FBXW4 | GRCh38.p7 | 10:101695332 | GGTGGAAGCACAGGA[G/T]TTCGCGCTGCAAACA | 6468 |
rs371354165 | snp | C/T | 3.31098e-05 | 0.00406864 | synonymous-codon, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101611309 | TGGGTTTTGAAAATC[C/T]AGGACGTGGAGGTTG | 6468 |
rs371405228 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101666403 | AATGACGTGGCTAAT[C/T]GGCTCTAATTCTTAG | 6468 |
rs371412465 | snp | A/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101647287 | CCCCATCAGCTCTTT[A/T]CCACCAGGCCTCAGA | 6468 |
rs371516584 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101636082 | AGGCCAGGCGTGGTG[A/G]TTCACACCTGTAATC | 6468 |
rs371569418 | snp | A/C | 1.72039e-05 | 0.00293285 | intron-variant | FBXW4 | GRCh38.p7 | 10:101611420 | GAAGGCCTGGAAGGG[A/C]GGGCACAGGAAGTGG | 6468 |
rs371693826 | snp | A/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101662953 | TCAACTCTGGCCTTC[A/T]GGAAGAGAGAATGTT | 6468 |
rs371698322 | snp | A/G | 5.28723e-05 | 0.00514134 | intron-variant | FBXW4 | GRCh38.p7 | 10:101612503 | AAGGACGGAGTGAGA[A/G]GCTGCTCCACGTGGG | 6468 |
rs371732460 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101635006 | ACCTGTACCAGTCCA[C/T]GGCCTGTTAGCAACC | 6468 |
rs371741411 | in-del | -/CA | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101643449 | CCTTTGCTGAGAAGG[-/CA]CACACACACATACAT | 6468 |
rs371803376 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101690450 | GACTGACTCCAACTA[C/T]CTTTGTGTCCCTTTA | 6468 |
rs371910507 | in-del | -/AA/AAA/AAAA | 0.161596 | 0.233848 | intron-variant | FBXW4 | GRCh38.p7 | 10:101654119 | GCGAGACTCCGTCTT[-/AA/AAA/AAAA]AAAAAAAAAAAAAAA | 6468 |
rs371982569 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101617735 | AACATCTGTTGCCAT[A/G]AAGGGATAAGGAGAA | 6468 |
rs372059824 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101658662 | CACCTAATTGCAGGA[A/G]GATGGAGTGATCCTT | 6468 |
rs372079263 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101631753 | CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGAATAT | 6468 |
rs372092528 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101664521 | CTGACAACCATACTC[A/G]ACAGGAATGGTGGCA | 6468 |
rs372112497 | snp | G/T | 0.000809268 | 0.0200992 | intron-variant | FBXW4 | GRCh38.p7 | 10:101624838 | AGGAGAACAAAGTCA[G/T]ATCTGGCTTGTCAGA | 6468 |
rs372126329 | snp | G/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101670651 | CCTTACTTCTGAAGA[G/T]CCCAGGTGCCTCTGT | 6468 |
rs372240528 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101633840 | TCCAGGCTGGGCGTG[A/G]TGGCTTACACCTGTA | 6468 |
rs372240649 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | FBXW4 | GRCh38.p7 | 10:101656760 | AAACACAAGTACATG[A/G]AAAACATGGGGGTGG | 6468 |
rs372245303 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101667007 | GAGGCCGAGGCAGGC[A/G]GATCACGAGGTCAGG | 6468 |
rs372441911 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101634712 | AAAAATTAGAAGCCT[A/G]CCTCCCAGCAGATAT | 6468 |
rs372492389 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | FBXW4 | GRCh38.p7 | 10:101692695 | AGGAGGTGGTGAGCC[A/G]AGTGCACACCACTGC | 6468 |
rs372509135 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101660888 | CTATTTTACTTGTCG[A/G]TCTCTCCCATCAGAC | 6468 |
rs372526656 | in-del | -/A | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101631459 | AACTACTAAAAAAAA[-/A]GAGCCTATGCAGAGA | 6468 |
rs372564361 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101675586 | AACCAGTGCAAACTG[C/G]ATGCAAGCAGGAAAG | 6468 |
rs372669984 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101614067 | GATTCAGCCACCCTG[A/G]GCAGGCCAGAGCCCT | 6468 |
rs372688348 | snp | A/C/G | 1.64746e-05 | 0.00287002 | intron-variant | FBXW4 | GRCh38.p7 | 10:101667879 | CATCCAAATATGTCT[A/C/G]CCTTACCTGAGTAAT | 6468 |
rs372689468 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101687361 | ATTCCCCCTTCCAAC[C/T]CACACAGCCAGTGAG | 6468 |
rs372705732 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101674659 | AGTAAGTGTGGCAAT[A/G]GAAAAACACAGCCCC | 6468 |
rs372857514 | in-del | -/A | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101622727 | GTGAGACTTCATCTC[-/A]AAAAAAAAAAAAAAA | 6468 |
rs372892289 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101660333 | AAGTTGGGTTGGGAG[C/G/T]GGGGGTGGGTGCTGC | 6468 |
rs372894379 | snp | C/T | | | upstream-variant-2KB | FBXW4 | GRCh38.p7 | 10:101695656 | TAGATCCTGAGTCCA[C/T]AACTTCAAAAACAGT | 6468 |
rs372905244 | snp | A/G | 6.61583e-05 | 0.00575107 | synonymous-codon, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101611736 | GCAGTACAGGGTGCT[A/G]TCGTGGGGCTCCTCC | 6468 |
rs372938274 | snp | A/G | 3.30158e-05 | 0.00406286 | intron-variant | FBXW4 | GRCh38.p7 | 10:101668007 | AGAGGAGATGCTCTC[A/G]TTGGCATTGCCTGGG | 6468 |
rs372974913 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101620588 | GAGCGGGCAGGGCTG[C/T]TTCTTCTCAGGCTCC | 6468 |
rs373068345 | in-del | -/GA | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101616169 | CAACAATGGCTTTTG[-/GA]GAGAGAGAGAGGAGG | 6468 |
rs373162979 | snp | A/C | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101620799 | TGTCTCATACCTATT[A/C]TCATTAGAGTCCATT | 6468 |
rs373176948 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101685512 | TATTGCCCATGATAC[A/G]ATTTGCTGAAAATAA | 6468 |
rs373360560 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101626724 | CGATTTCTTGACCTC[A/G]TGATCCGCCCACCTT | 6468 |
rs373437570 | snp | C/G | | | missense, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101611699 | AACCTGTGGCCAGCA[C/G]GTGGTTGCCATCTGT | 6468 |
rs373454801 | snp | C/G | 3.29609e-05 | 0.00405948 | missense, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101611672 | ACAGCCGTACAACAC[C/G]GTAGTAGGAGGAACC | 6468 |
rs373561732 | snp | A/G | 1.78144e-05 | 0.00298444 | intron-variant | FBXW4 | GRCh38.p7 | 10:101611452 | AAGAGCTTTCCAAGT[A/G]GGACATGGGTGTGCC | 6468 |
rs373680065 | in-del | -/AA/AAA | 0.493432 | 0.0569306 | intron-variant | FBXW4 | GRCh38.p7 | 10:101676711 | GATGTCCAGATTGGG[-/AA/AAA]AAAAAAAAAAAAAAA | 6468 |
rs373692258 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101657361 | TATCTGGCCAGGCAC[A/G]GTGGCTCATGCCTGT | 6468 |
rs373757651 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101679706 | CCTTTATGCTTTTAC[A/G]TATTTTCTAATTTTT | 6468 |
rs373764985 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | FBXW4 | GRCh38.p7 | 10:101696416 | TACTTTTTGATCTTA[C/G]CAAAACAACAACAAA | 6468 |
rs373820445 | snp | A/G | 1.66496e-05 | 0.00288522 | missense, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101612415 | AAAGGGGACTCATAC[A/G]TGACATCCAGCACCC | 6468 |
rs373879191 | snp | C/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101651317 | AGAAAACAGAGGCCA[C/G]TGGGGTGGAGAGGGT | 6468 |
rs373881158 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101637360 | TCGTGCCACTGCACT[C/T]CAGCCTGGGCGACAG | 6468 |
rs373939687 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101657277 | AGGCAGAGGGATTTC[A/G]TCTGAGGCACACAAG | 6468 |
rs373941029 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101644178 | GCTTTTCAGCCTTTC[C/T]AGTGAATGGTGGGGA | 6468 |
rs373958028 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101641617 | ATTCACATAGTGCAT[A/G]TAAGATTTTTTCTCA | 6468 |
rs373975364 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101613437 | TTAGCTTCCTTTACC[C/T]GTGAGACGCTGGGCT | 6468 |
rs374153202 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | FBXW4 | GRCh38.p7 | 10:101635613 | GCCAAGGCAGGCAGA[C/T]TGCTTGAGCCCAGGA | 6468 |
rs374162563 | snp | A/G | 3.29799e-05 | 0.00406065 | missense, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101672922 | CACCTCACCTTGGCC[A/G]TCCTGTCCCTGGAGC | 6468 |
rs374292375 | in-del | -/AAAAC | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101641637 | TTTTTTCTCAAAAAA[-/AAAAC]AAACAAAACAATACA | 6468 |
rs374334071 | snp | A/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101640917 | CTCACTGCAACCTCC[A/T]CCTCCCAGGTTCAAG | 6468 |
rs374348313 | snp | A/G | 1.69123e-05 | 0.0029079 | missense, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101612365 | GGAGGTCCCAGTAGC[A/G]AACATAGGTGTCATA | 6468 |
rs374423339 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101628250 | AAAGAAAATTCAAAC[A/G]GCTTTTGCCCTCAGT | 6468 |
rs374429861 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101622792 | TTTGCAAATCACATA[C/T]TTGACAAAGGACTAA | 6468 |
rs374517094 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101678518 | GCAAGCTCCGCCTCT[C/T]GGGTTCACATCACTC | 6468 |
rs374619458 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | FBXW4 | GRCh38.p7 | 10:101689834 | CACTGAAATAGATAC[C/T]CCAGGCCCCCAGCCT | 6468 |
rs374659023 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101662685 | AGCACCTTTTTTTTC[C/T]TGGAGGGCAATACAT | 6468 |
rs374663611 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FBXW4 | GRCh38.p7 | 10:101631826 | TAGAGATGGGGTTTC[A/G]CCGTGTTAGCCAGGA | 6468 |
rs374774495 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101642220 | TGTGTTTAGGATATA[C/T]GTCTATGAATATATA | 6468 |
rs374798244 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101619519 | AAAAAATTAGCCAGG[C/T]GCGGTGGCAGGCACC | 6468 |
rs374802329 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101643064 | AATAGGAGAAGGCAG[A/G]GCTTTGCCAACAGGA | 6468 |
rs374849676 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101628223 | TGAAAAACCCAGCTC[A/G]GCTCAGAAAAGAAAG | 6468 |
rs374934048 | snp | A/C | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101627313 | AGGGAGAGAAAGCAG[A/C]GTGTCTTCCTGGCAC | 6468 |
rs375003948 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101687743 | ACAAAAGTCTAGGAA[A/C]AAATTCATCAATGGC | 6468 |
rs375010282 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101654053 | TTGAACCCTGGAGGC[A/G]GAAGTTGCAGTGAGC | 6468 |
rs375027816 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101645449 | TGTGTCTCACTTGTA[C/T]AGGACACCCTCTCCC | 6468 |
rs375141183 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101635898 | CATCCTGCCTTGGAG[C/T]CCACTTCCTCCCTAC | 6468 |
rs375205512 | in-del | -/A | 0.126219 | 0.217206 | intron-variant | FBXW4 | GRCh38.p7 | 10:101634234 | AATGAACAAATAAAC[-/A]AAAATCACTAGAAAA | 6468 |
rs375328628 | snp | A/G | 1.64751e-05 | 0.00287007 | intron-variant | FBXW4 | GRCh38.p7 | 10:101624724 | GGACTGGAAGCCAGC[A/G]TGGGCTCATGAATCT | 6468 |
rs375354562 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101688575 | AAGCTCAAATATTTA[C/T]ATGATTCAGGGTACA | 6468 |
rs375380017 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101660735 | TCCTGATGAGCAGAG[C/T]GGAAGAAAGAGTGGT | 6468 |
rs375415984 | in-del | -/TTCT | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101640480 | CTTTTCTTTCTTTCT[-/TTCT]CTTTTTTTTTTTTTT | 6468 |
rs375530355 | snp | A/G | | | intron-variant, upstream-variant-2KB | FBXW4 | GRCh38.p7 | 10:101695155 | GCCCGAGCCGCCACC[A/G]CCGCCGCCCCGGGAG | 6468 |
rs375576997 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101684204 | TCTCGGCTCACTGCA[A/G]CCTCCGCCTCCCAGG | 6468 |
rs375644082 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101612734 | TCACACCTGCGTGCC[A/G]GCTGCCACCCACCCA | 6468 |
rs375680273 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101648806 | CTCCCAGAAAGTCAG[A/G]TTTTCTGATCAGTAT | 6468 |
rs375692444 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101663780 | AGACATATGCCCCTC[C/T]ACCCCAGGCACGCCT | 6468 |
rs375715602 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101629038 | TGCCAGGGAGTTAGA[A/G]TTTGTGTATTCAAGT | 6468 |
rs375794766 | snp | A/C/T | 1.64887e-05 | 0.00287125 | intron-variant | FBXW4 | GRCh38.p7 | 10:101673478 | GGAAGGAGAAACCTA[A/C/T]AGCACTTACCCTCCT | 6468 |
rs375830463 | snp | A/C | 0.0429648 | 0.14013 | intron-variant | FBXW4 | GRCh38.p7 | 10:101612680 | CCAGTCCCAGGCCCC[A/C]CCCCTCCCCCAGCAT | 6468 |
rs375847291 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101668399 | GAGAGGGAAGAAGAT[C/T]AAGGCATAGTATAGG | 6468 |
rs375917849 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101652822 | ATTTGTCCACCATCT[A/G]CTCTGGCTGGCTGAT | 6468 |
rs375986749 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101614668 | TTCTCTAAAATGGCC[A/G]CACACACTTTAAATG | 6468 |
rs376076143 | snp | C/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101660732 | CCTTCCTGATGAGCA[C/G]AGTGGAAGAAAGAGT | 6468 |
rs376127302 | in-del | -/A/AA | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101692746 | GTGAAACTCCGTCTC[-/A/AA]AAAAAAAAAAAAAAA | 6468 |
rs376130002 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101644725 | CCAGGCACTCTCCAA[C/T]GCTACTCTGCTAATA | 6468 |
rs376131644 | snp | G/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101694189 | GGAGGCTGCCTCAGA[G/T]GGAGGCCTTGGGGAG | 6468 |
rs376145695 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101630224 | CCGAGGAAGGCTTTT[C/T]ATCTGAGCCTTATTA | 6468 |
rs376147845 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FBXW4 | GRCh38.p7 | 10:101678618 | TGTTTTTAGTAGAGA[C/T]GGGGTTTCACCGTGT | 6468 |
rs376178360 | snp | C/T | 8.31483e-05 | 0.00644727 | intron-variant | FBXW4 | GRCh38.p7 | 10:101672888 | GACAGGAGGGAGTAA[C/T]AGTATGTAAGGGGGA | 6468 |
rs376213119 | snp | A/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101641649 | AAAAAAACAAAACAA[A/T]ACACATACACCTTAA | 6468 |
rs376243805 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101693065 | CCAGGTGAAACAAAC[A/G]CATGGGAATATATTT | 6468 |
rs376288847 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101639503 | TCATTTGGCCTTTAT[C/T]CAACTAGTAGACACC | 6468 |
rs376294544 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FBXW4 | GRCh38.p7 | 10:101678584 | GTGCCCACCACCACA[C/T]CCAGCTAATTTTTTT | 6468 |
rs376329921 | snp | A/G | 0.000100319 | 0.00708164 | utr-variant-3-prime, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101611289 | AGGGGTGGCCCTGAC[A/G]GTCATGGGTTTTGAA | 6468 |
rs376335461 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101618001 | GGCCAGGCCCCTGCA[C/T]AAGGTGGGGGCAGAG | 6468 |
rs376472671 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101688287 | TGTCTCCAAGCCCTG[C/T]CTTCATTTCACAGTT | 6468 |
rs376507145 | snp | C/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101639859 | GGGTGTATTTCAGTT[C/G]TGCCTTTGGCTTGGT | 6468 |
rs376594302 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101643188 | ACCTCATCCAAACAA[C/T]ATGGGAGCAAGATTG | 6468 |
rs376707565 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101631697 | CAGTGGCGCAATCTC[A/G]GCTCACTGCAACTTC | 6468 |
rs376825442 | snp | A/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101692382 | AAAAGAGAATTACTT[A/T]ACAAAGTTGTAGACA | 6468 |
rs376892890 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101630545 | CATCTGCTAACCTCC[A/G]CCACTGACATCATTA | 6468 |
rs376910027 | snp | A/C/T | 0.000182134 | 0.0095413 | intron-variant | FBXW4 | GRCh38.p7 | 10:101673719 | CATCAAGATACAGTA[A/C/T]GAAAACTCAACTCCA | 6468 |
rs376993275 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101683704 | ACAACATAATCTCTG[A/G]GATCAGAAAACTCCT | 6468 |
rs377038129 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101668949 | GGTCCCAGCAGTGCT[A/G]TAAGGGGAACACACA | 6468 |
rs377068216 | in-del | -/C | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101641653 | AAACAAAACAATACA[-/C]ATACACCTTAAGTGT | 6468 |
rs377079260 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101683155 | CAGGAGCAGGTACCC[C/T]TTGGAATTCACCAGG | 6468 |
rs377096120 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101668443 | AATTAGGGAGAGAAG[C/T]AAAAAGAAACATGCA | 6468 |
rs377127804 | snp | A/C/G/T | 5.59879e-05 | 0.00529071 | intron-variant | FBXW4 | GRCh38.p7 | 10:101612307 | GGTGCAGGGCCCCCA[A/C/G/T]CACCTGTCCTCCCTG | 6468 |
rs377129637 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101616239 | TGCCTAGGGGACAGA[C/T]GGCTTGAAGGTATAA | 6468 |
rs377180481 | snp | C/T | 1.64743e-05 | 0.00287 | missense, intron-variant | FBXW4 | GRCh38.p7 | 10:101667935 | GGTCTTCAGTCTGGA[C/T]GGTGTGTAAGCACTG | 6468 |
rs377213279 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101617698 | AAGGGGCAGCCGCGT[A/G]GATAAAAGGATACAA | 6468 |
rs377225202 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101653949 | AACATGGTCAAACCC[C/T]ATCTCTACTAAAAAT | 6468 |
rs377324335 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FBXW4 | GRCh38.p7 | 10:101652370 | AGTCTCTCTTGCTTC[A/G]CCCTGGATACCAGTA | 6468 |
rs377352364 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101694228 | AAGGGGTCCCCGAGA[A/G]TGCTCGGGAAAGGGT | 6468 |
rs377362266 | snp | A/C | 1.6483e-05 | 0.00287076 | missense, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101611681 | CAACACCGTAGTAGG[A/C]GGAACCTGTGGCCAG | 6468 |
rs377428719 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101676978 | AATACACAAGCCGTC[A/G]TCTGGGAGAAAAGAT | 6468 |
rs377442671 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | FBXW4 | GRCh38.p7 | 10:101640049 | GAGATGAGCAAAGGG[C/T]TTTGCCAGGCCTCTA | 6468 |
rs377613888 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101638070 | AAAAACTTTTTGGTG[C/T]GCTTCCTCCTCAATC | 6468 |
rs377628371 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101626928 | GATGAGGGTGGTGTG[A/G]GGATGTAAATCCCCT | 6468 |
rs377638888 | snp | A/C | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101676464 | AGAACAGATAATCCA[A/C]TCACTACAACTTATT | 6468 |
rs377655126 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FBXW4 | GRCh38.p7 | 10:101622261 | GAGAAGAGCATCTTC[A/G]CCAGTGCTGTCAAAT | 6468 |
rs377753883 | snp | A/C | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101664244 | ATACATAAGAAGATA[A/C]GGTAGAAAAGTCCCA | 6468 |
rs377755004 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101645068 | GTGCTACCCCAGCCT[A/G]CTCCTTCAATGGCCT | 6468 |
rs386372272 | in-del | -/TT | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101640485 | TTTCTTTCTTTCTCT[-/TT]TTTTTTTTTTTTTTT | 6468 |
rs386372273 | in-del | -/TT | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101640506 | TTTTTTTTTTTTTTT[-/TT]TGAGAGAGAGAGTCT | 6468 |
rs386372275 | in-del | -/AA | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101676712 | ATGTCCAGATTGGGA[-/AA]AAAAAAAAAAAAAAA | 6468 |
rs386747079 | multinucleotide-polymorphism | GTCCATAAATGTAC/TTCCATAAATGTAT | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101654710 | TATGACATCTTTTGG[GTCCATAAATGTAC/TTCCATAAATGTAT]ATCTGTGTCATCCTT | 6468 |
rs386747080 | multinucleotide-polymorphism | AGC/GGT | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101678587 | CCCACCACCACACCC[AGC/GGT]TAATTTTTTTTACTG | 6468 |
rs397689204 | in-del | -/A | 0 | 0 | intron-variant | FBXW4 | GRCh38.p7 | 10:101689146 | TGCAAAAAAAAAAAA[-/A]TGAAAGTATGGAGTA | 6468 |
rs397705226 | in-del | -/AACAA | 0 | 0 | intron-variant | FBXW4 | GRCh38.p7 | 10:101641648 | AAAAAAACAAAACAA[-/AACAA]TACACATACACCTTA | 6468 |
rs397744866 | in-del | -/A | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101674340 | CAAAAAAAAAAAAAA[-/A]GAAAGAAAGAAATCT | 6468 |
rs398014629 | in-del | -/A | 0 | 0 | intron-variant | FBXW4 | GRCh38.p7 | 10:101642397 | GTTTTTTTTTTAATT[-/A]AAAAAAAAAATAGAG | 6468 |
rs527417767 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101668150 | AGCTTCTGGCTCACC[C/T]ACCCCCGCAGATAGG | 6468 |
rs527477459 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101651082 | TAATGCATGCGCCTC[C/T]GCACATTCCTTCGAG | 6468 |
rs527511537 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101688961 | AAACTAATCCAGTGC[C/G]AGGGTCAACCCAGAG | 6468 |
rs527513048 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101677319 | TAGGGTAGGTTCATA[C/T]AATGGAATACTACTC | 6468 |
rs527529856 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101651606 | GCCCTTCTCTGCCCC[C/T]CTCCTTCCCTCCCTC | 6468 |
rs527533274 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101642329 | GCCGAGGCAGGAGGA[C/T]TGCTTGAGGCCAAGA | 6468 |
rs527563653 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101667013 | GAGGCAGGCGGATCA[C/T]GAGGTCAGGTGATCG | 6468 |
rs527585741 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101688067 | AATATAATGTAAGGA[A/C]TGATTTGAAATCAGG | 6468 |
rs527593198 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101665257 | TAAAGACAGAATCTC[A/G]AACACAAACTATTTT | 6468 |
rs527632033 | snp | A/G | | | upstream-variant-2KB | FBXW4 | GRCh38.p7 | 10:101695578 | TAGGTTCTCACACAG[A/G]CCCGGAAGCACGGTC | 6468 |
rs527668417 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101644232 | AGCTGGAGCTGCTCT[A/G]TGCAAGCCAAACAAA | 6468 |
rs527731481 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101645083 | GCTCCTTCAATGGCC[A/T]GGGCTGGCTGCTAAG | 6468 |
rs527799086 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | FBXW4 | GRCh38.p7 | 10:101636990 | AAAATAATATGGGAC[A/G]GGAAAGTGTGTAGGG | 6468 |
rs527838982 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101690180 | TTTCAGTATCAGAAT[C/T]TGCAGATAGCGCTCC | 6468 |
rs527845867 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101619893 | GTTCTGTGAGAAGCA[G/T]CATTGGCTGTCTGAG | 6468 |
rs527874216 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101668867 | AAATCTCAGACGTAC[A/C]GGACTATCCCAAGAC | 6468 |
rs527905158 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101629441 | GGTGCGCACCACCAC[A/G]CCTGGCTAATTTTTG | 6468 |
rs527908384 | snp | C/T | 0.00279162 | 0.0372561 | utr-variant-3-prime, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101610809 | AGCAAAACCAGGCCA[C/T]AGTGCCCCAGGAATG | 6468 |
rs527995383 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101652928 | CTGTCTTTATTTCTG[A/C]ATTGTCCTTTGGTGC | 6468 |
rs528004992 | in-del | -/A | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101668641 | TATCTCCTACAGGTT[-/A]AAAATATTGCTTGGA | 6468 |
rs528062516 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FBXW4 | GRCh38.p7 | 10:101656767 | AGTACATGGAAAACA[C/T]GGGGGTGGGAAGGTC | 6468 |
rs528141948 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101649089 | GCAGCCCAGGGAATC[C/T]CCAAAGAGGCTGCTG | 6468 |
rs528186281 | snp | G/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101678103 | AAAACATTGGAGGGC[G/T]AGTGTCAATAGTACT | 6468 |
rs528201986 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101640620 | TCTTAGCCTCCCAAA[C/T]AGATGGGATTACAGG | 6468 |
rs528246546 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | FBXW4 | GRCh38.p7 | 10:101693997 | GGAACCTGAGTCCTA[C/G]ACCTGGACTCAAGGA | 6468 |
rs528264021 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101624020 | CAGTTCTGTACCTCA[A/G]TTGTGGTGATGGTTA | 6468 |
rs528272228 | snp | G/T | 0.000798403 | 0.0199641 | downstream-variant-500B | FBXW4 | GRCh38.p7 | 10:101610391 | GGGTGTGTGTTGGGG[G/T]AGGGGTCACCACAGG | 6468 |
rs528324999 | snp | A/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101643915 | AAAATGATTTTCTTT[A/T]ATTGCTTGGTGGGAA | 6468 |
rs528325527 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101614904 | GGGCCCTTCTCGGCC[C/T]CCACCCCAAGACCTA | 6468 |
rs528349327 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101664825 | AAACCCTGTCTCAAT[A/T]TGCATAACACATATA | 6468 |
rs528399262 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | FBXW4 | GRCh38.p7 | 10:101665544 | CACATCGAGACCTTA[C/G]CAGAGGGTCTGGCAC | 6468 |
rs528411189 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101656057 | ATGCATGTCACCTGC[A/G]CACTGAAACCCCACA | 6468 |
rs528426771 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | FBXW4 | GRCh38.p7 | 10:101616787 | CTCACCTGGCACAAA[C/T]TCCGTGAGTGGCAGA | 6468 |
rs528457632 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | FBXW4 | GRCh38.p7 | 10:101664746 | TCTGGTTGACATTAC[A/C]TTATAGCCCTTTTTG | 6468 |
rs528469828 | snp | A/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101616290 | AAAGAGAATGGGAGG[A/T]TTTTCCTCCCTTCTA | 6468 |
rs528505553 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101685470 | TCCACAATTTTACAG[A/G]GATTTCTATCAGACA | 6468 |
rs528544987 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101657889 | CCTTTATGATTCATA[G/T]GGTCTCTATAGCCAG | 6468 |
rs528553835 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101667006 | GGAGGCCGAGGCAGG[C/T]GGATCACGAGGTCAG | 6468 |
rs528597483 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101658869 | GATCCCTCTTTTGAC[G/T]GATCTGAGTGTTACA | 6468 |
rs528667458 | snp | A/C/T | 0.00358779 | 0.0422022 | intron-variant | FBXW4 | GRCh38.p7 | 10:101641231 | AATTAAAAGCATGCA[A/C/T]AATTGGATAGGAGAA | 6468 |
rs528667650 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101648414 | ACCAGATGATTTGAT[C/T]GACTAGACAGAACTT | 6468 |
rs528712952 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101633004 | CTGGCATGTTGCATA[C/T]AACAGTAGAAAGGGG | 6468 |
rs528727033 | in-del | -/G | 0.00199481 | 0.0315187 | utr-variant-3-prime, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101610764 | TCACTCAGAACTGCT[-/G]GGGTTCCCTTTGCTC | 6468 |
rs528734248 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101652123 | CGCTTCTCCTCACTC[C/T]GCCCTCCTCACCACC | 6468 |
rs528775945 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101625882 | AGCCCATCTGCTGTG[C/G]CCCAGCCCAGCACCT | 6468 |
rs528885849 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101621344 | CCAGCCTGGGCAACA[G/T]AGCGAGACCTTGTCT | 6468 |
rs528887828 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101611827 | TCCACCTCTACCCCA[A/G]CTTTCTTGGGCCTAG | 6468 |
rs528924768 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | FBXW4 | GRCh38.p7 | 10:101689847 | ACCCCAGGCCCCCAG[A/C]CTCAAAGAGCTCCAA | 6468 |
rs528941708 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101662320 | TGCTTTCCTTCCAGA[C/T]GCTCCCTCACCTCTG | 6468 |
rs528948104 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FBXW4 | GRCh38.p7 | 10:101612679 | ACCAGTCCCAGGCCC[C/T]ACCCCTCCCCCAGCA | 6468 |
rs528951865 | snp | A/C | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101673862 | ACTAGAGTAACTGAG[A/C]CTTGTGGTGATCTAA | 6468 |
rs529057113 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | FBXW4 | GRCh38.p7 | 10:101636417 | AAAAAAAACAAAAAA[A/G]AATTGCAAATTAGAG | 6468 |
rs529094105 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101641083 | TGATCCACCCACCTC[A/G]GCCTCCCAAAGTGCT | 6468 |
rs529129000 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101636930 | ATCTTTTAGAGTACA[C/G]ACTGAAATATTTATA | 6468 |
rs529191866 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101629751 | TTCTCATGTGGGCTA[C/T]ACTTCAAGAGTTAGT | 6468 |
rs529259414 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FBXW4 | GRCh38.p7 | 10:101638754 | TATTGCACAAACCAC[A/G]TGATATCTTGGCTCC | 6468 |
rs529320583 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101631399 | GCAAGAGACTTATGA[C/T]ATACTATTATAAGAG | 6468 |
rs529412680 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101683104 | GTCAAAGGGGGTCAG[C/G]AGAACAAGGCAGCAG | 6468 |
rs529473655 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | FBXW4 | GRCh38.p7 | 10:101682197 | TTTAGTTATAACTAT[C/T]AGAAATTGTTCCTCC | 6468 |
rs529490529 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101692554 | TGAGGTCGGCAGTTC[A/G]AGACCAACCTGACCA | 6468 |
rs529492956 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101654940 | GCAGTCCCCCCACCT[A/C]AGCCTCTTGAGTAGC | 6468 |
rs529515754 | snp | C/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101645271 | AGCCTCTTCTTTTTG[C/G]GGGGAAGCCCAGTCC | 6468 |
rs529634053 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101642276 | TGACAAGTGGCCAGG[C/G]ACAGTGGCTCACATC | 6468 |
rs529675263 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101647522 | CACTTGCTTTGGAAT[C/T]GATTTTTTTTCCCCC | 6468 |
rs529698102 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101619344 | GGCCTAACCCCATGG[G/T]ACCCAGTTCCAGAAG | 6468 |
rs529797865 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101658654 | CTGAGAGCCACCTAA[C/T]TGCAGGAGGATGGAG | 6468 |
rs529802357 | snp | A/C/T | 3.30968e-05 | 0.00406786 | missense, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101676420 | TCACTCGTTCCTTCA[A/C/T]TGGGACACTGGTCAT | 6468 |
rs529802634 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101635333 | GTTGTATAATTATTT[A/C]ATTATATATTACAAT | 6468 |
rs529804030 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101687927 | TCCATGAATGTCAAC[C/T]GGGGGCACAGGCAAT | 6468 |
rs529864908 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101687071 | GAACTCATTACAGGG[C/T]TAGTGAGCAGGGGAA | 6468 |
rs529891003 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101650328 | CAGACACTCTGCCTC[A/T]TTTCTGTCTGGTCTC | 6468 |
rs529935777 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | FBXW4 | GRCh38.p7 | 10:101695472 | GCCCCTCTAGAAGCC[A/C]TCCTCTTCCTCGAGT | 6468 |
rs529950573 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101650994 | CTCCCGCCTGGGCCC[A/T]GAGTTCGGCAGCCTT | 6468 |
rs530056684 | snp | G/T | 0.000399281 | 0.0141238 | downstream-variant-500B | FBXW4 | GRCh38.p7 | 10:101610575 | GAGGCTGGTCTTGTC[G/T]TTTCAGCAGCACATA | 6468 |
rs530088075 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101690907 | CTTTTGCTATATACA[A/G]ACTAACTAGAGGAGA | 6468 |
rs530101749 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101651889 | AAGTGAGATGAAAGG[A/G]GGCCGCGGCCCTCTC | 6468 |
rs530182050 | in-del | -/GTGGTG | 0.00159617 | 0.0282053 | intron-variant | FBXW4 | GRCh38.p7 | 10:101656261 | GCCAACATAATCAAA[-/GTGGTG]GTCACCCCATGCTTA | 6468 |
rs530222440 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FBXW4 | GRCh38.p7 | 10:101692720 | CACTGCACTCCAGCC[C/T]GGGCAACAAGAGTGA | 6468 |
rs530264493 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101658996 | TCCGCTCTACCATCA[A/G]GTTCCTCTTTAGCCT | 6468 |
rs530347780 | snp | A/C | 0.00914312 | 0.0669923 | intron-variant | FBXW4 | GRCh38.p7 | 10:101618903 | GGCAGAAAAAAAAAA[A/C]CCACAGCAAGAGGAA | 6468 |
rs530350558 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101660118 | GATTGAAGTGTGTGT[C/G]CCTTGAAGAGCTGAG | 6468 |
rs530352163 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101624691 | GAGGCTGGCTCAGCA[A/G]GCTTTCCCTCACCTC | 6468 |
rs530415975 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101644803 | GAGCTGCCCATAGCA[C/T]AGGCCACTGCTCTAC | 6468 |
rs530449150 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101668657 | AAAATATTGCTTGGA[A/G]CACATTATCTGGTCT | 6468 |
rs530453083 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101682308 | ATTATTCTGTTGGGT[A/G]AATGTAGTCCCTGGT | 6468 |
rs530475231 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101647109 | TGTCTGGCTTTCCCA[A/G]TGGAGGCTGCCAGAA | 6468 |
rs530506931 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101655162 | TGTAAGTCTTTGTAC[A/G]TATATCTTGCAGAAT | 6468 |
rs530549334 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101664290 | AAGATTAATATATCT[C/G]ACAAATTATTTTAAA | 6468 |
rs530572581 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101655897 | GACCAGGCACCACAG[A/C]TTGGACCCAGGGCAA | 6468 |
rs530619818 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101671281 | CTGCAAACCAGCTGA[A/C]CAGCTTGCAGGACCA | 6468 |
rs530645622 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101612832 | GCACATGCACACACA[C/G]ACACACACTTGGTTA | 6468 |
rs530751156 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101622466 | GGTGCGGTGGCTCAC[A/G]CCTGTAATCCCAGCA | 6468 |
rs530778770 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101625088 | CTCTGCACACCATAA[A/T]AACAGATCTCTAGAC | 6468 |
rs530878487 | snp | A/G | 5.29694e-05 | 0.00514606 | synonymous-codon, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101612339 | CCAGCACACTCACCG[A/G]ACGCTGGTGCGGAGG | 6468 |
rs530901406 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101616682 | CCAGGCTGTTTTGGC[A/G]GCAGCTGGCAATCTG | 6468 |
rs530934540 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101674069 | GCACAGTGGCTCACA[C/T]CTGTAATCCTAGCAC | 6468 |
rs530954414 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101683409 | TCTCTCTCAGCTTTC[C/T]GGCACTTAGTAACCA | 6468 |
rs531030385 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101686399 | ATTTGATTACAGAAT[C/T]AGTTTTTCAAGAATC | 6468 |
rs531118968 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101655952 | AATTCCCCAATCAAT[A/G]AAGAAGCGAGGAAGG | 6468 |
rs531159540 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101652558 | ATAATAATAACGACA[C/G]GGTAGAACAATAGAA | 6468 |
rs531173489 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101628580 | AAAGCTAGTCATGTG[C/T]ACTGTGAAGTTGGTC | 6468 |
rs531189581 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FBXW4 | GRCh38.p7 | 10:101624184 | TGGTTTGATTATTAC[A/G]TATTATGTAAGATGT | 6468 |
rs531230966 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101685146 | GCTACTTCTGGGGAC[C/T]AGTCAAATTCATCCA | 6468 |
rs531234494 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101620004 | CTTTGAATGTGTCCC[A/G]GCCCCCACCATCATC | 6468 |
rs531236854 | in-del | -/CA | 0.00119737 | 0.0244387 | intron-variant | FBXW4 | GRCh38.p7 | 10:101614603 | CCCCTGCTCTGCCCG[-/CA]CAGCCTGGCAGGGGC | 6468 |
rs531273465 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101669090 | CTCTTCCCTATAAAA[C/G]GAGAAAGTGTTTTTT | 6468 |
rs531293689 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101689089 | GTCAGTTGGGGATTT[C/T]AGCAGCTCAAGCACA | 6468 |
rs531332028 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101661271 | GGCCAGCCAGGGCTC[A/G]GAGAGTGCTGGTCTC | 6468 |
rs531385187 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101643280 | GTGGCTGCTGGCCAT[C/T]GAGCCTTCAGTTGCC | 6468 |
rs531421276 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | FBXW4 | GRCh38.p7 | 10:101696710 | AATGCGGCCAAAGAA[C/T]TTAAGCCATGTTTTA | 6468 |
rs531434351 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | FBXW4 | GRCh38.p7 | 10:101620345 | AAAGACAGCTCTAGA[C/G]AGTCATCCTGTCCAT | 6468 |
rs531471329 | snp | C/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101660334 | AGTTGGGTTGGGAGG[C/G]GGGGTGGGTGCTGCA | 6468 |
rs531504082 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101627981 | AATGCTGTGCTCTGA[C/T]AACCTGTTCGATTTG | 6468 |
rs531505666 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101636379 | AGAACCAAAAAACAA[A/T]AACAAAACAAAACAA | 6468 |
rs531590281 | snp | A/C | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101632368 | TCCAACAAATAAGGG[A/C]CAGCAAAGCAGGGTT | 6468 |
rs531625692 | snp | C/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101664924 | ATTCTAGTAAGGTCT[C/G]TAAAGGAAATAGTAT | 6468 |
rs531649005 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101635007 | CCTGTACCAGTCCAT[A/G]GCCTGTTAGCAACCA | 6468 |
rs531712583 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101646097 | TCACTGGCCAGGCCA[C/T]AGAGCATCAATTGGG | 6468 |
rs531713881 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101638679 | CAAAATACTCATTTT[A/G]AAGTTACCTGAAAGA | 6468 |
rs531720642 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101630090 | AGTTCTCTTCAACCC[A/G]CATTGGCATTTTAAT | 6468 |
rs531770907 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101637679 | TACTCCAGCCTGGGT[A/G]ACAAAGCAAGATCCT | 6468 |
rs531773773 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101680985 | TGACAAATGTGAGGA[C/T]TGCAAAACATTTTGG | 6468 |
rs531780371 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101662234 | CAACACACAGTAAAC[C/T]CTGTAGCTACTGGGA | 6468 |
rs531805993 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101638942 | GCGTCATGAATTATA[C/T]ACAGTAGGACTACAG | 6468 |
rs531841344 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101630592 | AGCATGAATACAGTG[C/T]GAAGGTCACAAAAAC | 6468 |
rs531930075 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101645273 | CCTCTTCTTTTTGGG[A/G]GGAAGCCCAGTCCAA | 6468 |
rs531996379 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101650150 | TGCAGCAAGGTGAGT[A/G]GTAAAGACAGAAGAC | 6468 |
rs532058138 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101641365 | TTTTCAGAATTAAAG[C/T]TTAAAAATACACATC | 6468 |
rs532122726 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101640829 | CCTAGACTCTTCCTT[C/T]CCCCACCCCCGCCTT | 6468 |
rs532168463 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101665763 | TATTGACACCATCTT[A/C]AATAGTTGTTGTGCC | 6468 |
rs532171105 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101619972 | TGGGAGCGCTGGTGC[C/T]CAGTGGGTGGCTACA | 6468 |
rs532195262 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-5-prime, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101694753 | CATTCCTCCTTCTTC[C/T]CATACTCTCTTCCTT | 6468 |
rs532293816 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101657692 | AACTTCTAAAGAGTC[C/T]TGTTCAAGAAACTGC | 6468 |
rs532354187 | snp | A/C | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101690573 | AAAGTGGCCAGAATG[A/C]CTTCAAGCACAAGTA | 6468 |
rs532390045 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101656967 | ATTTGCATTGAAAAC[C/G]ATGAAAAGGAAAGCT | 6468 |
rs532428805 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101656670 | ATTGTTCTAAAAGCT[A/G]GATTATGGCTTTGCT | 6468 |
rs532434785 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101676182 | TCTTTAAAATGTGAA[A/G]AAGTTGTCCTTCTGA | 6468 |
rs532452383 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101649267 | TAAAGGTTATGATGT[A/G]CCATTGCCCTCCCAG | 6468 |
rs532514582 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101651780 | AGACCCCAATCAAGA[C/T]CCCCATGTCACAGGT | 6468 |
rs532541802 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101658997 | CCGCTCTACCATCAG[A/G]TTCCTCTTTAGCCTT | 6468 |
rs532590170 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101629650 | ATTTGCTCTAGCTCA[C/T]ACAGGTAGCAACTAG | 6468 |
rs532666960 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FBXW4 | GRCh38.p7 | 10:101668380 | TTTACTTTGGAGAAG[C/T]AGGGAGAGGGAAGAA | 6468 |
rs532693425 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101617539 | GGTGAGAAGGAAGGG[C/G]CTTCTCAAGCATACA | 6468 |
rs532713418 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101625996 | GGTGGGGAGGTTGGC[C/G]TGCCAGTTGCTGATG | 6468 |
rs532778601 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101616884 | CAAGAGTCACAGACA[A/G]AAAGTGACAATGTCG | 6468 |
rs532786519 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101613572 | TTTTGGCCCAAGTAG[A/C]ATGTCAGCAAAGGGC | 6468 |
rs532787716 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | FBXW4 | GRCh38.p7 | 10:101626754 | TGGCCTCCGAAAGTG[C/G]TGGAATTACAGGCGT | 6468 |
rs532846252 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101654510 | TGCCTGATATTAAAA[G/T]AGACATTTAAATGTA | 6468 |
rs532880068 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101679817 | ATGATGAAGTCTGGA[C/T]TTTTAGTATGCCAGT | 6468 |
rs532885139 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101667059 | ACACAGTGAAACTCC[A/G]TCTCTACTAAAAATA | 6468 |
rs532944409 | in-del | -/C | 0.00358779 | 0.0422022 | intron-variant | FBXW4 | GRCh38.p7 | 10:101685919 | GCTCCAAAGGCCCTT[-/C]CTTAAAATGTGTAAC | 6468 |
rs532952120 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101663042 | AAGGCACAGCAATGA[A/C]AAAAGGCCTGCTTGT | 6468 |
rs533015723 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101620715 | ACTCCTGAGCTCAAG[C/T]GATCCTACTGCCTCA | 6468 |
rs533016720 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101664112 | AGAACTCAAAGTAAA[A/G]TAAGAAAGGAAAGAA | 6468 |
rs533030302 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101637869 | GTGGTCTGCAAAGTC[A/G]ACCCCGTAATCACTA | 6468 |
rs533041532 | snp | C/T | 0 | 0 | intron-variant | FBXW4 | GRCh38.p7 | 10:101690944 | ACAATTAAAAAGTTC[C/T]GTTTTACAATTTATT | 6468 |
rs533069807 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101655105 | AAAGTGCTGGGATGA[C/T]AGGTGTGTGCCACCA | 6468 |
rs533131721 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101631848 | TAGCCAGGATGGTCT[C/T]GATCTCCTGACCTTG | 6468 |
rs533152085 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101672842 | CTCAGCCAATCCTGA[A/G]ACTCAGGGATCTATC | 6468 |
rs533189227 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101630505 | GGAGTCATTAGAACA[C/T]GTCAGGTCTCATTGC | 6468 |
rs533189937 | snp | A/C | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101668641 | TATCTCCTACAGGTT[A/C]AAAATATTGCTTGGA | 6468 |
rs533192877 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101692218 | AAAATAGTATGGAAA[C/T]GGAAAACTGTATCAG | 6468 |
rs533221685 | snp | A/G | 0.000102077 | 0.0071434 | intron-variant | FBXW4 | GRCh38.p7 | 10:101673069 | GAGAAATAAGGAGCC[A/G]ACCCCCAAGAACCAA | 6468 |
rs533251886 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101621433 | CTTGGGAGGCTGAGG[C/T]AGAAGGACCATTTGA | 6468 |
rs533263874 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101625012 | CCCCCAGTGGTGCCT[G/T]GCCAGAAGACCCACG | 6468 |
rs533295875 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101673785 | AGGATAACCAACAAG[A/G]CTTATTATCTATACT | 6468 |
rs533315277 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101692641 | ATGCCTGTAATCCCA[G/T]CTACGCAAGAGGCTG | 6468 |
rs533395592 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101638897 | CCAAACTTCTGCTTC[A/G]TAACCACTCTGTTTG | 6468 |
rs533412957 | snp | A/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101678760 | CGAGCCTCTACTTAT[A/T]CCGTCACATTTGCCA | 6468 |
rs533457286 | snp | A/G | 0 | 0 | intron-variant | FBXW4 | GRCh38.p7 | 10:101639629 | TTAATCAAGAGATGC[A/G]CAGCTGACCCAAAAC | 6468 |
rs533464113 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101614990 | AATAGCCCCAAACTT[A/T]GGGGGAAAAGGGGAC | 6468 |
rs533553118 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101646925 | AGTCCCAGTGGAGCC[A/G]GAGTTGGTCTCAAGA | 6468 |
rs533683513 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101659388 | GACTCGTGCAGTAAA[A/G]TCCAGGCTCCAAGGG | 6468 |
rs533742325 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101617177 | TAATCCTCACAACAG[A/G]CTTTGGAGGTAAGTT | 6468 |
rs533803968 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101617993 | TGACTGTGGGCCAGG[C/G]CCCTGCACAAGGTGG | 6468 |
rs533811896 | in-del | -/T | 0.0023933 | 0.0345097 | intron-variant | FBXW4 | GRCh38.p7 | 10:101682898 | CTTTGTTAAAAACAA[-/T]TTTAACAACTCAGCT | 6468 |
rs533828971 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101676638 | TTAAACTATCAAAAA[C/T]GTTCACAGTGATGCC | 6468 |
rs533934270 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, missense, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101694429 | AGCGAGGCCCGGGCT[A/C]TCCGGCGCCAGAGCA | 6468 |
rs533976208 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101632650 | AGTGGAATAACATAA[G/T]TTCATTCATCCTATT | 6468 |
rs533985541 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101628252 | AGAAAATTCAAACGG[C/T]TTTTGCCCTCAGTCC | 6468 |
rs534013801 | snp | G/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101670888 | AAGGAAGAGGGTTCT[G/T]TGGACAGTCCCTAGC | 6468 |
rs534063550 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101691410 | CCGAGCAGTGACCCT[A/G]CTCTTTATCAAGTGC | 6468 |
rs534125985 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101651334 | GGGGTGGAGAGGGTG[A/G]GAAATGGGTGGGGGG | 6468 |
rs534170214 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101635876 | AGATGGAGGGGCACC[C/T]CTCCAGCATCCTGCC | 6468 |
rs534189734 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101670101 | AGCAGACTGGTGATA[C/T]GCATCACAACTTTTA | 6468 |
rs534234588 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101636576 | GTATGATAATGGTAT[A/T]ATGATTACTATCTTT | 6468 |
rs534264777 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | FBXW4 | GRCh38.p7 | 10:101696915 | TTCCTGCATTTTGTG[A/T]TTAGATTTGTGTTAG | 6468 |
rs534312464 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101629078 | AAAAATAACAAGACA[C/T]AGAAAAGAGGAAAGC | 6468 |
rs534423822 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101689419 | TGTCCTGCTTCCACA[A/G]GTGTACTGTTTTATT | 6468 |
rs534426210 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101631891 | CTTGGCCTCCCAAAG[G/T]GCTGGGATTATAGGC | 6468 |
rs534465365 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101652018 | CCGAATGGGGAGGAG[A/G]GGAGAGATTCCCTCC | 6468 |
rs534576921 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101688056 | CTGGGGGAGAAAATA[C/T]AATGTAAGGAATGAT | 6468 |
rs534581279 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101639221 | GGGTGCTAGGCCACT[G/T]CTCATTCATACAACC | 6468 |
rs534658400 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101631682 | GCCTAGGCTGGAGTG[C/T]AGTGGCGCAATCTCG | 6468 |
rs534702320 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101657256 | CATTTTACTAGGGCA[C/G]CCCAGAGGCAGAGGG | 6468 |
rs534724595 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101623348 | AGGCCAGAAGTTCAA[A/G]ACCAGCCTTGGCAAT | 6468 |
rs534753095 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101649539 | GGGAGTGCCTATTTC[C/T]CAATGAAAGAAATGT | 6468 |
rs534810926 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | FBXW4 | GRCh38.p7 | 10:101680235 | AATTTAAAAGTTTAA[A/C]TAGAAGAAAACAAAA | 6468 |
rs534815654 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | FBXW4 | GRCh38.p7 | 10:101640982 | ATTACTGGCACCCGC[C/T]ACCACACCCAGCTAA | 6468 |
rs534875727 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101612940 | GGGGCTCAAACCTCA[C/T]TGGGGATAAAGACCA | 6468 |
rs534877040 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101624283 | GTTAAAAAAAAAAAA[A/C]AAACCAGAATGGCAG | 6468 |
rs534940449 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FBXW4 | GRCh38.p7 | 10:101647275 | AGGTCGTTCTGCCCC[C/T]ATCAGCTCTTTTCCA | 6468 |
rs535051082 | snp | A/C | 0.00318978 | 0.0398085 | utr-variant-3-prime, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101611058 | CCGGGTTCAGCCGCA[A/C]TCTAAAGCAGCAGGT | 6468 |
rs535084255 | snp | A/C | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101682641 | AGACAGCACTTCTCT[A/C]ACCTCCCTGGTCACT | 6468 |
rs535140568 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101653152 | CCCTCTCTCCCTGAT[A/G]TGCAGTCATGTCTGA | 6468 |
rs535196340 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101653819 | CAGCAGCATTCAATA[C/T]ATCCATAAGACAGGC | 6468 |
rs535197871 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101644653 | GGAAGCTTCAGGGAA[A/G]AAGATTCTCCCAGAA | 6468 |
rs535238794 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | FBXW4 | GRCh38.p7 | 10:101673370 | CTGCTTTAAATGGAA[A/C]ACCCTTCTGGTCTCC | 6468 |
rs535246625 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101646107 | GGCCATAGAGCATCA[A/G]TTGGGATTCTTGATC | 6468 |
rs535251102 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, synonymous-codon | FBXW4 | GRCh38.p7 | 10:101628026 | CTTCAACCAGATTCT[C/G]GTCACATCCCTCACG | 6468 |
rs535362772 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101656423 | TCACATTCTACTTCA[A/T]CAAGCCTACCCGCTG | 6468 |
rs535366540 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101620049 | GCTTAGGGCAAACTG[C/T]CCCTCCAGTACTCCC | 6468 |
rs535390715 | snp | C/G | 0.000399281 | 0.0141238 | downstream-variant-500B | FBXW4 | GRCh38.p7 | 10:101610300 | ACAAAAAACAAAACA[C/G]AAACCTTGGAAGTAG | 6468 |
rs535403109 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101671781 | AGCCTGAAGTAAGTA[C/T]GAAGTAGGGTAATAG | 6468 |
rs535412538 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101680030 | TTTAGGATAATGGCC[C/T]CCAATTCCATCCAAG | 6468 |
rs535420091 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FBXW4 | GRCh38.p7 | 10:101660630 | TATCTGTTGGCAGAA[C/T]GGTGATCAAAGGTGG | 6468 |
rs535429635 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101661576 | CCACCTAGAATTACC[C/T]GGAGCTTCCATCTTT | 6468 |
rs535436884 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101691111 | CAAGTTTTGTGTAAT[A/G]CTGATAAAAACTCAT | 6468 |
rs535465395 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101670448 | GCAGGTATCAGGCAA[A/G]CAATAATGGTGATTC | 6468 |
rs535513249 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101636471 | ACACATAGTATTTAA[C/T]GTGTGCCCAAGTGCT | 6468 |
rs535527768 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101671640 | AGGAAGATGGCTAGA[A/T]TAAGACAGGAGTACC | 6468 |
rs535535464 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101677590 | TTTAAGTCTTGAGGG[G/T]GTTTGGGTTATACAA | 6468 |
rs535553828 | snp | A/C | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101669382 | TCCCTGACACAAACT[A/C]CCTGGGAGGCAGATT | 6468 |
rs535655106 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101636666 | AATCTCGGCTCTCTG[A/C]AACCTCTGCCTCCCG | 6468 |
rs535698205 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101639628 | ATTAATCAAGAGATG[C/T]GCAGCTGACCCAAAA | 6468 |
rs535777213 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101669304 | AGTCCTCTTTGGCAA[C/T]AACTAGATACATTTC | 6468 |
rs535797326 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FBXW4 | GRCh38.p7 | 10:101684590 | TTTATATTAACACTA[C/T]CTCTTGATTTCTCTT | 6468 |
rs535857775 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101694336 | CCTTTCCCGGGACGC[A/G/T]GGGCCGGCTCGGGGC | 6468 |
rs535947423 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | FBXW4 | GRCh38.p7 | 10:101613087 | GCTGGCCCCCAGCCC[C/G]GGGCTAGCACGCCTC | 6468 |
rs536000104 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101666687 | TATGTACTCTGCTGG[A/G]GAGGAGAGGGATTCT | 6468 |
rs536012418 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101661146 | TCCACAGTATTCAGC[C/T]GTCTGCAGGAGCCTC | 6468 |
rs536028867 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101649325 | AGTCACAGTGCTTTC[C/T]ACAATCCGGGAGCCC | 6468 |
rs536083950 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101675574 | TGATGCCAGTGAAAC[C/T]AGTGCAAACTGGATG | 6468 |
rs536091264 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | FBXW4 | GRCh38.p7 | 10:101679888 | TATCACTTACCCCCC[C/T]ACCTTCCTCCCTTCT | 6468 |
rs536092889 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101637155 | TTGGGAGGCTGAGGC[A/G]GGCGGATCACGAGGT | 6468 |
rs536110628 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101640890 | GGCTGGAGTACAATG[C/G]TGTGATCTTGGCTCA | 6468 |
rs536131758 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101685690 | ATTTTCTGAAACTTG[C/T]TTTTTTAAAAAAAAA | 6468 |
rs536155176 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101630041 | GCCACCAGAGCTGTC[A/G]CATCATTCACCAACA | 6468 |
rs536171757 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101632506 | AGAGCCTAGCCCAGG[C/T]TAGACAAAAGGAAGC | 6468 |
rs536194461 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101694760 | CCTTCTTCCCATACT[C/G]TCTTCCTTGTGCCTC | 6468 |
rs536237512 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101642647 | CAGTCTGTAGGCACC[A/C]AATTCTACCTCTGAA | 6468 |
rs536255048 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101674366 | AATCTTCTAGCCAAG[C/T]GAAATAACTTTCTTT | 6468 |
rs536295142 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FBXW4 | GRCh38.p7 | 10:101616192 | GAGAGGAGGGAAGGG[C/T]GACAAAAGAGTTGAC | 6468 |
rs536357550 | snp | C/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101653195 | TCCTACATAGTTTTC[C/G]TGAATGAAAGTTGTC | 6468 |
rs536437114 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101640034 | GAATGTCCTCACTGA[C/G]AGATGAGCAAAGGGC | 6468 |
rs536501718 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101631994 | CAGGGCCAAGGGCAG[A/G]CAGACCTGAAGGTGA | 6468 |
rs536597117 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101655439 | CTCAACCACAGCTCA[C/T]CCTGGATACTAGTAA | 6468 |
rs536692399 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101643343 | CAACTCCCAGGTGCT[A/G]GGATTTGGCCCCTGG | 6468 |
rs536697747 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101648875 | AAGGGAGGTTCCCAT[C/T]CCCACCAGAGCTTTT | 6468 |
rs536715540 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101627886 | AGTGCTTTGAAAAGG[A/G]GCTGGTGGGGTGGGA | 6468 |
rs536716601 | snp | C/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101621123 | ACTTTCATCAGAATG[C/G]CCATCTTTGTGACCC | 6468 |
rs536767721 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101630972 | TGCTTGTGGAACCTA[C/T]CATCCACAGTGGCAT | 6468 |
rs536838199 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101658331 | GCAGGTGGATCATAA[A/G]GTCAGGAGTTCAAGA | 6468 |
rs536851584 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101667217 | GGCTGGGTGACAGAG[C/T]GAGACTCCGTCTCAA | 6468 |
rs536857812 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101677137 | CCATTTTGGGAAAAG[G/T]TCTGGCAGTTTATTA | 6468 |
rs536906227 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101650833 | TAAAATCAACACTCC[A/G]TGAACACACAAAACT | 6468 |
rs536973452 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101645659 | TTGTGATAGACGCTG[A/C/G]GGTGTTCAAGAAAAA | 6468 |
rs537017365 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101615107 | TTTGTATAACGTGGT[A/G]ACCCCCCAAATTCAG | 6468 |
rs537112466 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101656230 | GTCTGAAGCTTCTCA[C/T]CTGATCACTTGCTAT | 6468 |
rs537193844 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101692254 | CACAATGAAGAGTTC[A/G]GATATAGATCCAATA | 6468 |
rs537216050 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101612229 | CTTCCTTCCCAGCCC[G/T]GACATGGAGTCTCTG | 6468 |
rs537228610 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101631658 | TTTGAGACAGAGTCT[C/T]GCTCTGTCGCCTAGG | 6468 |
rs537288573 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101623054 | AAATAAACACATGAC[A/C]ATATATTAACATAAT | 6468 |
rs537307324 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101653952 | ATGGTCAAACCCCAT[C/G]TCTACTAAAAATGCA | 6468 |
rs537324320 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101680741 | ATTCAGCAGGTACAG[C/T]CTTTCAGAAAGGAAT | 6468 |
rs537382127 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101673138 | AGCCCAAGTCTCCAG[C/T]GACATCCAAATTTGC | 6468 |
rs537513123 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | FBXW4 | GRCh38.p7 | 10:101660504 | TGGCTCCCCTTCACC[C/T]TCCCGCCTCCCTCTC | 6468 |
rs537627568 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101626431 | AAATCATTCGAGCAG[A/G]CAATTGGACTCTCCA | 6468 |
rs537681922 | snp | A/C | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101616847 | TTGTCCTAGTCCAGG[A/C]CCCGATTGTAGATAA | 6468 |
rs537692756 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101654508 | GCTGCCTGATATTAA[A/G]ATAGACATTTAAATG | 6468 |
rs537716277 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, downstream-variant-500B | FBXW4 | GRCh38.p7 | 10:101625423 | TCCCCAGAAGCCAGG[C/T]AGCCAGGGCTTCTGG | 6468 |
rs537723440 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101672499 | AACACATTTTAATTA[C/T]CAGCCTGATTGCTTA | 6468 |
rs537752787 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | FBXW4 | GRCh38.p7 | 10:101618319 | GAAAGGGCCACCAAC[C/T]CCAGCCACAGGGGTC | 6468 |
rs537755619 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101622509 | GAGGCAGGCTGATCA[C/T]GAGGTCAGGAGATCG | 6468 |
rs537784633 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101664496 | CCAGGGTCATATCAT[A/G]TTAGTGACACTGACA | 6468 |
rs537788465 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FBXW4 | GRCh38.p7 | 10:101651409 | CTAGCAATTTGGGGG[C/T]GGGAAAAGAAAGCCT | 6468 |
rs537798583 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101689438 | TACTGTTTTATTTTG[A/G]ACCTGTAAACTAAAC | 6468 |
rs537811170 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101619411 | CACCTGTAATCCCAG[C/T]ACTTTGGGAGGCCGA | 6468 |
rs537849859 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101668191 | CCATCCTAACTACCC[C/T]CTTTTACTTCCACTG | 6468 |
rs537880949 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101630635 | GGGAAGCCAGGAGCA[C/T]AGCTGCAGTGACAGC | 6468 |
rs537891919 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101620185 | ACCGCCCAACCCCAA[A/G]TCCTGCCGGCAATGC | 6468 |
rs537929894 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101691615 | GATTCATTCCCAATA[C/T]CTCTCTTTTAGAGCA | 6468 |
rs537956623 | snp | A/C/G | 3.33646e-05 | 0.00408429 | missense, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101611388 | ACAGGGCTGCTGAGG[A/C/G]GAGTCGACGTCAGCG | 6468 |
rs538044417 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101643494 | CTCCCTTCGGTAAGA[A/G]GGCACCCAGGATGCC | 6468 |
rs538136035 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101690311 | GTTTGTCCTCTTACT[C/T]TTTAGGGAAAATTTG | 6468 |
rs538143914 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101678717 | ACAGGCATGAGCCAC[C/T]GCGCCCGGCGAGATA | 6468 |
rs538281163 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101629987 | TGGCCCAGGCCCCAG[C/T]AGCCTCTGAGCCTGG | 6468 |
rs538344546 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101620952 | CCCTTCACCAAGGCA[A/T]CCATAGGCAGAAGAG | 6468 |
rs538356058 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | FBXW4 | GRCh38.p7 | 10:101625349 | TGAGAAAAGGAAAAA[A/C]TATGAAAGATGAGTG | 6468 |
rs538374625 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101670099 | AAAGCAGACTGGTGA[A/T]ACGCATCACAACTTT | 6468 |
rs538446342 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101656198 | TCTTGTCTAGCTCAG[A/C]AGCTAGAAAGAAACC | 6468 |
rs538481977 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101644482 | TTATGAAGCAAGGAA[C/T]AGGAAAAAGATGGCA | 6468 |
rs538497207 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101636075 | GCAAATTAGGCCAGG[C/T]GTGGTGGTTCACACC | 6468 |
rs538511704 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101648458 | CCTTGAGCAAGCACC[C/T]TGGATCAGAGTTTTC | 6468 |
rs538515803 | snp | C/G | | | intron-variant, missense, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101694433 | AGGCCCGGGCTATCC[C/G]GCGCCAGAGCAGATC | 6468 |
rs538530752 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FBXW4 | GRCh38.p7 | 10:101694078 | GGCAGCTAAACCTCT[A/G]CAAAAACACACAATC | 6468 |
rs538548202 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101636637 | TTGTTGCCCAGGCTG[G/T]AGTGTAATGGTGCAA | 6468 |
rs538560747 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101649062 | TACAATTATATTTTT[A/G]AAGGAAAAAAGGCAG | 6468 |
rs538610737 | in-del | -/TCCT | 0.00199481 | 0.0315187 | intron-variant | FBXW4 | GRCh38.p7 | 10:101615932 | CCTGTACTAGAGCAC[-/TCCT]TCCTGAGTCACCACC | 6468 |
rs538616397 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FBXW4 | GRCh38.p7 | 10:101631917 | TAGGCGTGAGCCACC[A/G]TGCCCAGCCATTATT | 6468 |
rs538648686 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101650599 | AGCAAGTGTGTGCTC[C/G]AGCATCCCAAGGTGC | 6468 |
rs538666070 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101624620 | GGCACCACAGCAGAG[A/G]CCTCCTACTAGACCA | 6468 |
rs538704349 | snp | C/G | 1.65362e-05 | 0.00287538 | intron-variant | FBXW4 | GRCh38.p7 | 10:101673459 | GTATAAGATGGAAAA[C/G]GGTGGAAGGAGAAAC | 6468 |
rs538728750 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FBXW4 | GRCh38.p7 | 10:101615265 | AGCCCCAGGCCAAGA[C/T]GGGAGCAAGGGCCAG | 6468 |
rs538775234 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | FBXW4 | GRCh38.p7 | 10:101642448 | AGGTTCCTCTGAAGT[C/T]CCATCTCCTTACAGG | 6468 |
rs538826780 | in-del | -/G | 0.00199481 | 0.0315187 | intron-variant | FBXW4 | GRCh38.p7 | 10:101689383 | CAGTTCGCATTTGGA[-/G]GTAGTGATTGCACTA | 6468 |
rs538833903 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101622952 | TGCAAATACATGAAG[C/T]GTTCCATTAAAAGAA | 6468 |
rs538949492 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101639955 | GGTTTCTGTCACTTA[A/C]AATAAATGTGTCCTG | 6468 |
rs539050875 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101621657 | GGGAAACTCTTTCAC[A/G]ATAATTTTGTTCATA | 6468 |
rs539141128 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101642500 | CACAGTGAGCTGCCC[C/G]TTCCTGCTCCTCTCC | 6468 |
rs539162474 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101637274 | GTGGGCACCTGTAGT[C/T]CCAGCTACTTGGGAG | 6468 |
rs539245919 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | FBXW4 | GRCh38.p7 | 10:101695094 | GGGCCCCGAGCGGCC[C/T]TGGCTGCCCATGAGC | 6468 |
rs539282974 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101611122 | CATCTCTGGTAAGCT[C/G]CAAAGTCCCAGGAGT | 6468 |
rs539283336 | snp | A/C/T | 0.00119737 | 0.0244387 | intron-variant | FBXW4 | GRCh38.p7 | 10:101633058 | GCCACCTAGTAATCA[A/C/T]GTGATCCAGAGTGAG | 6468 |
rs539304863 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101666537 | GGACCAAGTCTCTTA[C/T]AAAATAAGCAACTGA | 6468 |
rs539314135 | in-del | -/TG | 0.00199481 | 0.0315187 | intron-variant | FBXW4 | GRCh38.p7 | 10:101647818 | TTTCTCCACAGTACC[-/TG]TGCCAGGTGCTAGAC | 6468 |
rs539322307 | in-del | -/CAGCTACAC | 0.00755907 | 0.0610114 | intron-variant | FBXW4 | GRCh38.p7 | 10:101660465 | CGGCTGCTCAGAGAA[-/CAGCTACAC]CAGCCACAGAATTTA | 6468 |
rs539330157 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101678251 | GTACGCCTTTGAAGA[G/T]AATTTTGAAATCATG | 6468 |
rs539345022 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101649633 | GGCCCCTCAAAGACC[C/T]TGGAGCTCCAGCTTC | 6468 |
rs539346089 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101612103 | TGACAGTACCCTGAC[A/G]GCTCCAGAGGCTCTG | 6468 |
rs539380282 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FBXW4 | GRCh38.p7 | 10:101653227 | TCCCACTGTCCCTAC[A/G]AGTCTGGTCCCTTCC | 6468 |
rs539390401 | snp | A/G | | | intron-variant, downstream-variant-500B | FBXW4 | GRCh38.p7 | 10:101625504 | GCCGAGAGGCACACG[A/G]GAAGGAGCAGGCTGA | 6468 |
rs539425283 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101622812 | CAAAGGACTAATATC[C/T]AGAATACAGAAAGAA | 6468 |
rs539452474 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101672459 | GCTGCTTACTGACCA[C/T]ATCACTCTCCAGAGA | 6468 |
rs539473670 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101645568 | AAGATTTTGCCTGGG[C/T]AATCCCTGAGCGGGG | 6468 |
rs539486264 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101631838 | TTCGCCGTGTTAGCC[A/G]GGATGGTCTTGATCT | 6468 |
rs539513828 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101664413 | AGAAATTGGCAGGTA[A/C]ACCAGGAGTACCTGC | 6468 |
rs539542397 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101662068 | AAGGACTGCAGCACC[A/G]CTGGCAACCAAAAGA | 6468 |
rs539592322 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101620088 | GCCCAAGCCCCAGCA[C/T]ATACATAAAAGAGAA | 6468 |
rs539631215 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101638128 | TGGAAAGATACCTGA[A/C]CATATGTAAAAATAG | 6468 |
rs539649564 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101669375 | TGCCTTTTCCCTGAC[A/G]CAAACTCCCTGGGAG | 6468 |
rs539712897 | in-del | -/CT | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101639401 | ACAGTTCCTATCAGA[-/CT]CTTCACTTTGTTTAA | 6468 |
rs539713335 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101661739 | GGGACACCAAGCCAC[G/T]CTTTGACTAGCTCTT | 6468 |
rs539795752 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101613147 | CCAGCCTGCTCCCCC[C/G/T]ACCCTCACCCCACCC | 6468 |
rs539851144 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101657407 | GGAGGCCAAGGTGGA[C/T]GGCATCACCTGAGGT | 6468 |
rs539904442 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101623228 | GGACTAGCCTGGGCA[C/T]GATGGCAAACCCATC | 6468 |
rs539906025 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101691304 | TCAGTGGCTTATTAA[C/G]TCTCTGCAGCTGTCC | 6468 |
rs539914089 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101649981 | GAAGTTTTGCTCTCC[C/T]CAGAAGCAGAGCAGA | 6468 |
rs539940505 | snp | C/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101619558 | CAGCTACTCGGGAGG[C/G]TGAGGCAGGAGGATG | 6468 |
rs539954078 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101655395 | TTTGAATAATTTGTG[G/T]TTTTTTTTCCTATTA | 6468 |
rs540000082 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101684065 | ACCTCCCAGACTCAA[A/G]TGATTCTCCTGCCTC | 6468 |
rs540042009 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101624881 | AATGGCTAACAATGG[C/G]AAATGCCGTGCTCAT | 6468 |
rs540055383 | snp | A/G | 0.000120697 | 0.00776749 | intron-variant | FBXW4 | GRCh38.p7 | 10:101673684 | TCTGACTGAAATGAT[A/G]GAAAAGAAAATTTAA | 6468 |
rs540117603 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FBXW4 | GRCh38.p7 | 10:101674426 | AAGTGGGAAGTTTCA[A/G]GGTTCTAGGATTCCC | 6468 |
rs540136726 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101621919 | TCAACTTGCTTGTCT[C/T]TTGTCTAGGATCACA | 6468 |
rs540261316 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101651497 | GTGGTGAATCAGGGA[C/T]GGTTTATCAAACAAT | 6468 |
rs540325782 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101673733 | ATGAAAACTCAACTC[C/T]AATCTTTGAAGAAGC | 6468 |
rs540352693 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101650882 | CACACATCGGATACA[A/G]AGATCGGGCTCTCGA | 6468 |
rs540393874 | snp | C/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101626452 | GGACTCTCCAGATTT[C/G]AGGAGTGGGGGCCAG | 6468 |
rs540469085 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | FBXW4 | GRCh38.p7 | 10:101625508 | AGAGGCACACGAGAA[A/G]GAGCAGGCTGACCCT | 6468 |
rs540480640 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101615404 | TCCGCCGAGTCAAGT[C/T]CAGCAATTCTCTCTC | 6468 |
rs540510666 | snp | A/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101663242 | TTAAGGCACTTAGTA[A/T]AATCTGGCAATCATT | 6468 |
rs540593944 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101626662 | ACCCAGCTAATTTTT[A/G]TATATTTAGTAGAGA | 6468 |
rs540597313 | in-del | -/A | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101619658 | GCAAGACTCTGTCTC[-/A]AAAAAAAAAAAAAAA | 6468 |
rs540607248 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101627271 | CCTTTTCTCTCACCT[A/G]ACCACTATGAATCAA | 6468 |
rs540609885 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101621390 | AAAGTTAGCCAAGCA[C/T]GGTGGGGCATGTCTA | 6468 |
rs540629649 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | FBXW4 | GRCh38.p7 | 10:101696022 | GGATACGCTGTATTG[A/G]GCTAAATACAATATA | 6468 |
rs540656762 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | FBXW4 | GRCh38.p7 | 10:101631149 | AAATAAAAAGAAGTT[C/T]CATTTCACACAGCAA | 6468 |
rs540674135 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101622392 | TTTAGATTCCATCAA[A/C]ATTTTAAACATTTGC | 6468 |
rs540877261 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | FBXW4 | GRCh38.p7 | 10:101693710 | GTTTAAGTGGTTCAG[-/A]AAAGTTTTTCATTCA | 6468 |
rs540889683 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101633932 | CCAACATGGTGAAAC[C/T]CTGTCTCTACTAAAA | 6468 |
rs540936410 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101663122 | ACTCCTCTTCTGCCC[C/T]ATTCCACATGTGGCC | 6468 |
rs540944231 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101672411 | GCAATTTGGCAAAGA[C/T]GCAACAAACAACACC | 6468 |
rs540967814 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101687738 | GAACAACAAAAGTCT[A/G]GGAACAAATTCATCA | 6468 |
rs540973830 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101676146 | AAAGTCATTTGTTAA[A/C]GTACATTTCTTGTAT | 6468 |
rs541022390 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101648596 | CATGGACAGAACCAG[C/T]GCCTTGCCTGGACAG | 6468 |
rs541027546 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101690841 | CAGTGCGTGTGTGTG[A/C]GTGTTCTTCCCTTTG | 6468 |
rs541076060 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FBXW4 | GRCh38.p7 | 10:101631370 | CTTTTAAATGATGTT[C/T]CCAAATAATACAAGC | 6468 |
rs541087669 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101640203 | GTTCTCTTATACCAA[A/T]GCCTAAGAACAGTGC | 6468 |
rs541107394 | snp | A/C | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101637668 | TCATGGCACTGTACT[A/C]CAGCCTGGGTGACAA | 6468 |
rs541108556 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | FBXW4 | GRCh38.p7 | 10:101672176 | CTATTGGGCCTCCTG[A/C]ACCACCAACTGAATT | 6468 |
rs541162489 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101663997 | TGCCACTTTCCTTTG[A/G]AGCCTGCTGGTTCTC | 6468 |
rs541171919 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101672712 | TCCCAGCCACTGTCC[A/C]CTCCTTTCCCAGTCC | 6468 |
rs541189221 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101632182 | AGGTCTGGGACACCT[C/G]TCCCAGTACACATAC | 6468 |
rs541199323 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101614073 | GCCACCCTGGGCAGG[C/G]CAGAGCCCTGTAGGG | 6468 |
rs541222841 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101645966 | CCTTTTGTAAACTGA[G/T]GATGATGATGGTACC | 6468 |
rs541240203 | snp | A/C | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101653657 | TCCTGTCAATAACCC[A/C]AGTAGTTGCTAGCAC | 6468 |
rs541274662 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101693414 | AATAGTAGAGGGATG[G/T]TCTTTAATCTCATTA | 6468 |
rs541281340 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101637561 | AAAAATACAAAAATT[A/T]GCCAGGTGTGGTGGT | 6468 |
rs541314207 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101681450 | AGGCTGGGCGCGGTG[A/G]CTCACGCCTGTAATC | 6468 |
rs541333903 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101655737 | TGGGAGAAAGAGACA[A/G]TGAGTCTCGTGCTCT | 6468 |
rs541359460 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101647920 | CCAATATTCTGCTAT[C/T]CCTCTGTGGAAAAGC | 6468 |
rs541423088 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101652323 | CAAATGGCAACATCC[A/G]TGGTCAGTAGCTTTT | 6468 |
rs541517535 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101639953 | TTGGTTTCTGTCACT[C/T]ACAATAAATGTGTCC | 6468 |
rs541522109 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FBXW4 | GRCh38.p7 | 10:101635345 | TTTCATTATATATTA[C/T]AATATAATAATAATA | 6468 |
rs541583398 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101627629 | GGGCGTGCGCACATG[A/C]AATCTCAGGGTACAA | 6468 |
rs541621555 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101655042 | ACTCTGTTGCCCAAG[C/G]TGGTCTTGAGCTCTT | 6468 |
rs541630387 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101687945 | GGGCACAGGCAATAT[C/T]TCTCTTTGCTGAGGA | 6468 |
rs541667295 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101658769 | TTTTACTCATTCTCA[A/T]TAGAAACCCCTACCC | 6468 |
rs541682150 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101692621 | TTAGCTGGGTGTGGT[A/G]GTGCATGCCTGTAAT | 6468 |
rs541729793 | snp | A/C | 0.00119737 | 0.0244387 | upstream-variant-2KB | FBXW4 | GRCh38.p7 | 10:101696464 | GCCTTTTAGTGTTCT[A/C]AATCTGTAGTGGAGA | 6468 |
rs541754861 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101651570 | TCTGCAGATGTGCTT[C/G]ATGAGTTAGGGACAA | 6468 |
rs541902081 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101678168 | GAGAGCACACAAGCT[A/C]CAGGAATGGCACTGT | 6468 |
rs541927388 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FBXW4 | GRCh38.p7 | 10:101636108 | TAATCCCAGCATTTT[A/G]GGAGGCTGAGGTGGG | 6468 |
rs542017000 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101667650 | ATATAGTACTCTTTC[C/G]TTAACATTTCTGAGG | 6468 |
rs542034941 | in-del | -/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101660332 | GAAGTTGGGTTGGGA[-/G]GGGGGGTGGGTGCTG | 6468 |
rs542078358 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101659741 | GCTTTATCAAATTCA[A/G]TCAGTAAGCTATTTC | 6468 |
rs542101976 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101629443 | TGCGCACCACCACGC[C/G]TGGCTAATTTTTGTA | 6468 |
rs542139526 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101668789 | AGCACAGGGCTCCCC[C/G]CTCACTTCACCCTAC | 6468 |
rs542215742 | snp | C/T | 6.75402e-05 | 0.00581081 | synonymous-codon, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101611402 | GGGAGTCGACGTCAG[C/T]GGGAAGGCCTGGAAG | 6468 |
rs542268223 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101665529 | TCACCAAAGATGAGA[C/T]ACATCGAGACCTTAG | 6468 |
rs542299035 | in-del | -/T | 0.00398564 | 0.0444627 | intron-variant | FBXW4 | GRCh38.p7 | 10:101630566 | ACATCATTACAGCAG[-/T]TAAGTCCCAAAGCAT | 6468 |
rs542315366 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101653431 | CTAGACTCCAAATTT[C/T]CCCTCCAGCGAGCCA | 6468 |
rs542355163 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101692522 | GCACTTTGGGAGGCC[A/G]AGGTGGGCAGATAAC | 6468 |
rs542375047 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101644968 | GGAGCAGTTTGGCAC[A/G]TGGTTTGTAGGTGGT | 6468 |
rs542385013 | snp | A/C | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101657598 | GAGATCATCATCACG[A/C]CACTGTAGTCCAGCC | 6468 |
rs542392008 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101628429 | CTTCCCATCTCCCCT[C/T]TGAGATCAGAATCCT | 6468 |
rs542441712 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101631817 | TATTTTTAGTAGAGA[C/T]GGGGTTTCGCCGTGT | 6468 |
rs542487271 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | FBXW4 | GRCh38.p7 | 10:101619855 | GGGCTGAGGGAACAA[A/T]GGTGACCCTGAAAGG | 6468 |
rs542548217 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | FBXW4 | GRCh38.p7 | 10:101610593 | TCAGCAGCACATACA[A/G]CCCTGAGCTTGGGTC | 6468 |
rs542548222 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101620221 | CACCTCTCGGATTGG[C/T]CTGTCAGTCAGGCTT | 6468 |
rs542656058 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101626544 | CACCAGGCTGGAGTG[C/G]AGTGGTGCAATCTTG | 6468 |
rs542708078 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101661979 | GCCAGAAAAAGAAAA[A/C]CTCAGAGGCACAATC | 6468 |
rs542718696 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | FBXW4 | GRCh38.p7 | 10:101656756 | GCCTAAACACAAGTA[C/T]ATGGAAAACATGGGG | 6468 |
rs542719511 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101617315 | AATGCAGCCACTCCA[C/T]CACTGGCCCCTCAAC | 6468 |
rs542768761 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101681366 | GCACTCCAGCCTGGG[C/T]GACAAGAGCGAAACT | 6468 |
rs542781972 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | FBXW4 | GRCh38.p7 | 10:101649004 | TCCCTGGGTGCTCCA[A/C]AAAGTTACCAAGAGC | 6468 |
rs542799921 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FBXW4 | GRCh38.p7 | 10:101666977 | TGGCTCACAACTGTA[A/G]TCCCAGCACTTTGGG | 6468 |
rs542888478 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101623985 | GGGTAAATGAGGAAT[C/T]TTTGTGCTGATGGAA | 6468 |
rs542907454 | snp | C/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101693053 | AGAGACAGTCTCCCA[C/G]GTGAAACAAACACAT | 6468 |
rs542910224 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101641122 | AGGCATGAGCCACCG[C/T]GCCCAGCCAACCCTT | 6468 |
rs542954677 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101664767 | GCCCTTTTTGAGGAT[A/C]ACTTGAGGCCAGGAG | 6468 |
rs542960122 | snp | A/G | 4.94328e-05 | 0.00497131 | missense, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101624793 | TGCCCGCAACAAGCC[A/G]TCCCTGTCACAAAAG | 6468 |
rs542968188 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101643425 | TCTGGGTTGTCCTGA[C/T]CTTGCCATCCTTTGC | 6468 |
rs542991739 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101633837 | AAATCCAGGCTGGGC[A/G]TGGTGGCTTACACCT | 6468 |
rs543005539 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101629627 | ACTGAGGCTTTGGGA[A/G]GTAATTAATTTGCTC | 6468 |
rs543068804 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101620422 | CTCAATCGCTGTACC[A/G]CTTGGTCCTCCAAGC | 6468 |
rs543070333 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101613820 | TGCTGCTGCCAGGGG[A/G/T]GAATTAATCCCCAAG | 6468 |
rs543132259 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101621280 | ACCTATAATCCCACA[A/G]CTTTGGGAGGCCAAG | 6468 |
rs543200999 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | FBXW4 | GRCh38.p7 | 10:101640594 | CTTCCTGGGTTCAAG[A/C]GATTCTTGTGTCTTA | 6468 |
rs543242866 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101649774 | GCCTCCCCAGGGCCA[C/T]CTCATCTCAGCGGCC | 6468 |
rs543259591 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101675874 | AACCTTTAGATCCTA[C/T]CCTGCCTTTTAATAA | 6468 |
rs543283430 | snp | A/C | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101689395 | GGAGGTAGTGATTGC[A/C]CTAGACCATGTCCTG | 6468 |
rs543322855 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101674985 | TCATCCCCAAGAACA[A/G]CCACCATCTCCTATT | 6468 |
rs543348855 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | FBXW4 | GRCh38.p7 | 10:101695213 | CATGGGGCGGCGCGG[G/T]CCGAGCCCTGGGCAC | 6468 |
rs543553020 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | FBXW4 | GRCh38.p7 | 10:101670942 | TTTTACTTCCCTTTA[C/G]CCCATAAAATAAATC | 6468 |
rs543601350 | snp | A/C | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101672860 | TCAGGGATCTATCCA[A/C]CCCCTCCCTATAGAC | 6468 |
rs543613775 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101691994 | TAAAAACGAAATGCA[C/T]AACATTTTCGGAAAT | 6468 |
rs543616823 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101680443 | ATTTTAACTAACACT[A/G]TAGATATAAGTTTTC | 6468 |
rs543643854 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101653304 | CCAAAGAATCCTATA[C/T]GCTGTAGCACAACAT | 6468 |
rs543665657 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101672024 | CAGTCAGAGAAGTTA[A/C]TGAGTAAAGATTGCA | 6468 |
rs543683076 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | FBXW4 | GRCh38.p7 | 10:101654263 | AAGGGAAGATCTTCT[C/G]AAAGTGTTAGAAATG | 6468 |
rs543732204 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101663799 | CCAGGCACGCCTCCA[C/G]CATCTCATTCCTGGG | 6468 |
rs543741341 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | FBXW4 | GRCh38.p7 | 10:101654874 | TGTCACCAAGGCTAG[A/G]GTGCAGTGGCACGAT | 6468 |
rs543856809 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101638713 | GTTGCATATTAGTAG[C/T]ACACTGAATTAAATG | 6468 |
rs543868244 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | FBXW4 | GRCh38.p7 | 10:101650972 | TAACGCCACTATGCC[A/G]GCAAATCTCCCGCCT | 6468 |
rs543937289 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101642245 | TATATACACATTTAA[A/C]AATTGAAGCAAAACA | 6468 |
rs543975803 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101612675 | TGCAACCAGTCCCAG[A/G]CCCCACCCCTCCCCC | 6468 |
rs544016470 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101666413 | CTAATCGGCTCTAAT[G/T]CTTAGAAAGAAAAAA | 6468 |
rs544054887 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101616679 | CAACCAGGCTGTTTT[A/G]GCGGCAGCTGGCAAT | 6468 |
rs544213003 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101688614 | TTCTTAATTACCATA[A/G]CCATTTTGATTCAAT | 6468 |
rs544274935 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101687886 | GTTATCCTTCAGCCT[C/T]TCAGCTGAGACCACC | 6468 |
rs544281942 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101675741 | GAGTCAAATAATAAC[C/T]ATGAAATCATTTAGC | 6468 |
rs544293738 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101677150 | AGGTCTGGCAGTTTA[C/T]TATAAATCTAAACAT | 6468 |
rs544320340 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101642916 | GTGATCTGGGGGTAC[A/G]CACATACATACATAC | 6468 |
rs544340200 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | FBXW4 | GRCh38.p7 | 10:101696209 | AGGAAGGATTGGAGA[C/G]TTTTCTTTTGTACTT | 6468 |
rs544353293 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101634226 | AAGAGAAAAATGAAC[A/G]AATAAACAAAAATCA | 6468 |
rs544546023 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101678065 | GTACAATTCATTCAA[C/G]TTTTCTGAGTTTTAA | 6468 |
rs544574502 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101619663 | GACTCTGTCTCAAAA[A/C]AAAAAAAAAAGAAGA | 6468 |
rs544594625 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101618751 | GGGCTGTGACTGTGG[C/T]TGGACCTACTATGAC | 6468 |
rs544607220 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101668618 | AGCTTAACTCTTTTA[A/G]GCTTCCATATCTCCT | 6468 |
rs544616685 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101692466 | TTAACTATTAAAAAA[A/T]TAAATTAGGCCAGGC | 6468 |
rs544635829 | snp | A/T | 0.000399281 | 0.0141238 | downstream-variant-500B | FBXW4 | GRCh38.p7 | 10:101610506 | AGGGATAGGTCATCA[A/T]TGGGAACTCTTCCTG | 6468 |
rs544653889 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101623761 | AAGAGGAATGCACTA[C/T]TGATACATGCAGCAA | 6468 |
rs544692745 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101672840 | CTCTCAGCCAATCCT[C/G]AGACTCAGGGATCTA | 6468 |
rs544693041 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101692516 | ATCCCAGCACTTTGG[A/G]AGGCCGAGGTGGGCA | 6468 |
rs544753047 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101652553 | AAAAAATAATAATAA[C/T]GACAGGGTAGAACAA | 6468 |
rs544756986 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101661989 | GAAAAACTCAGAGGC[A/G]CAATCTTTACTTTTG | 6468 |
rs544757491 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101644213 | TTGGCATGTGGGAAC[A/G]GTGAGCTGGAGCTGC | 6468 |
rs544765586 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FBXW4 | GRCh38.p7 | 10:101636809 | GGTCAGGCTGGTCCC[A/G]AACTCCTGACCTCAG | 6468 |
rs544776444 | snp | C/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101656013 | TACATTTCACTTTAC[C/G]TCACACATCTCAGCT | 6468 |
rs544875298 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101627618 | AAGATTAGAAAGGGC[A/G]TGCGCACATGCAATC | 6468 |
rs544939473 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101628282 | CCATCTCTTCCCTCA[A/G]GGGTATTCCAGGGAC | 6468 |
rs544940233 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | FBXW4 | GRCh38.p7 | 10:101618381 | TGTTTATATTGAAGA[C/G]CGAGCAGGGTTTCAT | 6468 |
rs544972244 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101672263 | GGGCTGTTGGGCACA[A/C]GCCTGGAGAAAGACT | 6468 |
rs544999874 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101682022 | TAATATTTCACACAA[C/T]TGTTTTTTAAAATGA | 6468 |
rs545021539 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101682817 | AAAACACTTGGCTGT[A/C]GTCCTTCAAATTTAG | 6468 |
rs545050983 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101632726 | CTGGATTTCCATCTA[C/T]ATGGCCCCTTAAACA | 6468 |
rs545102207 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101664688 | TACAGACTTGACAGC[A/C]GTTGAAGCCACTAAG | 6468 |
rs545113570 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | FBXW4 | GRCh38.p7 | 10:101625640 | CAGTGGGCCAGGCTG[C/G]CTGTAGTGCTGGCCT | 6468 |
rs545161471 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101655790 | GAAGGGCCATGATGC[C/T]GTAAGTCTGGGATGA | 6468 |
rs545163410 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101665306 | TCAATTCTGGAGTTA[A/G]GGGAAGACCATCTTA | 6468 |
rs545212433 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FBXW4 | GRCh38.p7 | 10:101638607 | TTAGAACATATTTAT[A/G]TATCACTTATGTATA | 6468 |
rs545284324 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101684958 | AGCTGACTGAACTGA[C/G]CCACAGCTCCCTTGA | 6468 |
rs545303383 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101622455 | ACAAGCAGCCGGGTG[C/T]GGTGGCTCACGCCTG | 6468 |
rs545307450 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FBXW4 | GRCh38.p7 | 10:101652094 | TCCTTCTTTGCTTCC[C/T]ATCTCCACCCCCTCG | 6468 |
rs545309548 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101614344 | CACCCTGGTCCCTGG[A/G]TTCAGAGGGAAGGAG | 6468 |
rs545337578 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101631729 | GTCTCCCAGGTTCAA[A/G]CAATTCTTCTGCCTC | 6468 |
rs545373025 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101641053 | CCAGGCTGGTGTCGA[A/T]CTCCTGACCTCAGGT | 6468 |
rs545384034 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101636167 | CCAGCCTGGCCAACA[C/T]GGTGAAACCCCATCT | 6468 |
rs545386011 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101644796 | CACAGCTGAGCTGCC[C/T]ATAGCACAGGCCACT | 6468 |
rs545533006 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101628460 | TTAGAGGCTCTTGGG[C/T]ACTGTACTGTCTAGC | 6468 |
rs545686004 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101651667 | CCTCCACTGCCTCCC[A/G]GGCCCTCCCCTCCCT | 6468 |
rs545689445 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, synonymous-codon, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101694521 | CATGTCCAGGTAGGA[A/G]CAGATGAGCAGCAGC | 6468 |
rs545721477 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101643714 | CAGTTTTCTCCCCCT[C/T]AGGCCAGTCTCTGTC | 6468 |
rs545751636 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101689000 | AAGTTGTCACACACA[C/T]GTAATTCTTTTCTAA | 6468 |
rs545826578 | snp | C/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101623923 | TTGCCAGGAATCAGG[C/G]ACAATGGGAAGAGGA | 6468 |
rs545856233 | snp | A/C | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101658273 | GGTTTGAGGCCGGGC[A/C]TGGTGGCGCACATCT | 6468 |
rs545898155 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101629561 | AGTTCTGGGATTAGA[C/T]GCATGAGCCACCGCA | 6468 |
rs545989656 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101689641 | TGTTTTCTGAAGATC[A/T]CAGTTTAGGCCTTAA | 6468 |
rs546002494 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101669850 | AGCTCCGCCTCCTGG[A/G]TTCATGCCATTCTCC | 6468 |
rs546011086 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101646737 | ACCCAGCAAATAAAG[A/C]CACAGGGAGAGGGAG | 6468 |
rs546029527 | in-del | -/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101627047 | CCCTGTACAGGGCCT[-/T]TTTTTTTTTTTTTTT | 6468 |
rs546065713 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101662178 | TTCACTAAAGAAAGA[C/T]GTATTTCAACAGGCC | 6468 |
rs546119802 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101621200 | TCACCTCCGCCTCCA[C/T]TAGTCACTAAGACAC | 6468 |
rs546177619 | in-del | -/A | 0.00318978 | 0.0398085 | intron-variant | FBXW4 | GRCh38.p7 | 10:101628747 | CACCTAAAAATTAAC[-/A]TCAAAACACACACAG | 6468 |
rs546183827 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101654115 | ACAGAGCGAGACTCC[A/G]TCTTAAAAAAAAAAA | 6468 |
rs546224947 | snp | C/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101615266 | GCCCCAGGCCAAGAC[C/G]GGAGCAAGGGCCAGC | 6468 |
rs546246900 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101646019 | TATAAAGTGGTCAGC[A/C]TAGTGCCTGGCACTT | 6468 |
rs546326252 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101678996 | ACACACACACACAGA[C/T]AGTATGAAAGGTTAA | 6468 |
rs546354937 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101620279 | CCTGCCTGTTCATTA[C/T]CTTAATCCTATTTTC | 6468 |
rs546475135 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101694020 | CTCAAGGAATCGTCC[A/G]AAGCACCGTACCAGA | 6468 |
rs546493594 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101664863 | CCTTTTAGCTTTTCA[G/T]AGTATTAATATTTTC | 6468 |
rs546558985 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101656104 | GCCCCCACAGTTCCA[C/T]AGTATTCTCTACTAC | 6468 |
rs546623607 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101649098 | GGAATCCCCAAAGAG[G/T]CTGCTGTACTCTTCC | 6468 |
rs546625275 | snp | G/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101666807 | AGGTGCAGTGGCTCA[G/T]GCACTTTGGGAGGCC | 6468 |
rs546683044 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101640703 | GGTTTTGCTGTATTG[A/G]TCTCAAATGGTCTCA | 6468 |
rs546691880 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FBXW4 | GRCh38.p7 | 10:101657947 | TCTACTAGTGTACAA[C/T]ATGGTGCCTATTCTC | 6468 |
rs546729126 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101664385 | AACTGCATAAGGGAG[A/C]AACAAAGGGTTGAGA | 6468 |
rs546793856 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101656332 | AACACAGACATAAGT[A/G/T]TCTCCAGCCTGGAAC | 6468 |
rs546803165 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101614969 | AGAGGGAGAGATTGG[C/T]CCGACAATAGCCCCA | 6468 |
rs546814363 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FBXW4 | GRCh38.p7 | 10:101684417 | AGGCGTGAGCCACTG[C/T]GCCTGGCCTACCCAG | 6468 |
rs546841483 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101615782 | AAACCTGGATAGCCC[G/T]CCAGGGACAGGCCCT | 6468 |
rs546886231 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | FBXW4 | GRCh38.p7 | 10:101620254 | GTGTTACTGAAAGAT[A/C]AAACTTTGTCCTGCC | 6468 |
rs546968776 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101666520 | CCTAAACGAAGTGGG[C/T]AGGACCAAGTCTCTT | 6468 |
rs546974525 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101611876 | TAAGGAGCCATTCCG[G/T]GATGGAAGAGAAAGA | 6468 |
rs547032633 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101667028 | CGAGGTCAGGTGATC[A/G]AGACCATCCTGGCTA | 6468 |
rs547050153 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101658916 | ATCTTCTTAAATATA[C/T]GAGTATTATCATGAC | 6468 |
rs547093516 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101624888 | AACAATGGGAAATGC[C/T]GTGCTCATTCCCTAG | 6468 |
rs547132556 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101645427 | TCCTGTGCCCCTGTG[A/T]CAGTCCTGTGTCTCA | 6468 |
rs547145643 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101690012 | TCAAAGGCTATTTAA[A/G]ATAAAATTCCTATTT | 6468 |
rs547155893 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101663006 | TATGGGCCACAGCTA[A/C]CATCCAAGATGCTGG | 6468 |
rs547217558 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101654389 | ATTTTATGATATATA[A/G]ATTCTACTTCAATAA | 6468 |
rs547228049 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101665478 | GGACAGGAAGACCCT[A/G]AAGATGAATGGGAAG | 6468 |
rs547242626 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101674252 | GAGAATCGCTTGAAC[C/T]TGGGAGGCGGAGGTT | 6468 |
rs547251367 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101620059 | AACTGCCCCTCCAGT[A/G]CTCCCCGCTCTCTGC | 6468 |
rs547254855 | snp | C/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101629049 | TAGAGTTTGTGTATT[C/G]AAGTTGAGAGATTAA | 6468 |
rs547274107 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101636977 | TGATATTTGCTTCAA[A/T]ATAATATGGGACGGG | 6468 |
rs547310822 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101620577 | CAGGCTGGCCAGAGC[A/G]GGCAGGGCTGTTTCT | 6468 |
rs547312618 | snp | A/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101611076 | TAAAGCAGCAGGTCC[A/T]GCCTCTCCAACAGGT | 6468 |
rs547359139 | in-del | -/A | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101677880 | ATATATTTTTTTCTT[-/A]AAAAAAAAAACCCAT | 6468 |
rs547372491 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101670001 | ACCTCATGATCCACC[C/T]GCCTCAGCCTCCCAA | 6468 |
rs547435048 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101671089 | TGTAGAATTTCAGAT[G/T]CCACTGAAAAGAAAT | 6468 |
rs547446698 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101653848 | GCACTCGGGGCCAGG[C/T]GCAGTGGCTCACGAC | 6468 |
rs547472266 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | FBXW4 | GRCh38.p7 | 10:101631520 | TAAAAGTGATTGTGT[C/G]TGGGCAGTAGAATGA | 6468 |
rs547566793 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101628871 | CTTACCAGAAGCCAG[C/G]CTTCTATAATTTCTC | 6468 |
rs547588144 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FBXW4 | GRCh38.p7 | 10:101646320 | GGGGCCTTAAAGGGG[C/T]AGACTGGAATTTGAG | 6468 |
rs547592349 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101683107 | AAAGGGGGTCAGGAG[A/T]ACAAGGCAGCAGAAG | 6468 |
rs547649533 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101638073 | AACTTTTTGGTGCGC[C/T]TCCTCCTCAATCCAG | 6468 |
rs547686280 | snp | A/C | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101667419 | CCAGCTGGATCTGGG[A/C]CCCAAGCCTCTCCTG | 6468 |
rs547705214 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101669344 | CTTTTAGGCAGCCCA[C/G]CTAAAAAGACAGCTT | 6468 |
rs547719656 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101638799 | AGAGACCCTTTACCT[C/T]GATGGCTTTCTGAGT | 6468 |
rs547719798 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101681057 | AATTTATAAAGGTAG[A/G]GGTGGGGAGACACTA | 6468 |
rs547873697 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101694820 | CCTTGACGATGCCTC[A/T]CGCCCCTTCCTCCAC | 6468 |
rs547883465 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101658658 | GAGCCACCTAATTGC[A/G]GGAGGATGGAGTGAT | 6468 |
rs547936247 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FBXW4 | GRCh38.p7 | 10:101613714 | ATCTTCCCGAAGGCC[A/G]AAGGAATCAAAGGAG | 6468 |
rs548051839 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101687196 | CCCATCCTCATCCCC[A/C]CTACAAAACCCACAG | 6468 |
rs548096105 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101630750 | AGTGTGAGACAACCA[G/T]TTCCTAAGATCCAGC | 6468 |
rs548115740 | snp | C/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101660546 | CCACTGAAATTTAAA[C/G]ACAGAAAAAAAAGAA | 6468 |
rs548205366 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101626119 | AGGCCATACGAGCTA[C/T]CCTGGGGCTTTCATG | 6468 |
rs548224337 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101633318 | GACATCAATGAAGCT[G/T]GAAACCATCATTCTC | 6468 |
rs548230662 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101626858 | ATCAAGGTAAATCAA[C/T]AGAGAGGGGAGCAAC | 6468 |
rs548257074 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101693729 | GTTTTTCATTCACAG[A/G]TCTCAGACCCTACCA | 6468 |
rs548328112 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FBXW4 | GRCh38.p7 | 10:101617919 | GAAAAAAAGCTATCA[A/G]TAATGCTTTCAAAGG | 6468 |
rs548450111 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101667225 | GACAGAGCGAGACTC[A/C]GTCTCAAAAAAAAAA | 6468 |
rs548497259 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | FBXW4 | GRCh38.p7 | 10:101695522 | CCACATGTGAGGGCC[C/G]AACGAATCTGCAGCC | 6468 |
rs548515087 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101659333 | AGATAAGTCATGGAT[A/G]GTTTGAGTGGCTTAG | 6468 |
rs548556099 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | FBXW4 | GRCh38.p7 | 10:101696792 | ACTACTAAGGCAGGA[A/G]TACTTCACATTTAGG | 6468 |
rs548611652 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101643359 | GGATTTGGCCCCTGG[A/G]AAGAGAGAGAACATG | 6468 |
rs548672881 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101644062 | GGGCTCTCCCCACAG[A/G]GGGCCTTTGTTCCCC | 6468 |
rs548783414 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101668051 | AGAGGTGCTCCGGGA[A/G]AGGTGACTGTTGGAG | 6468 |
rs548784660 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101618905 | CAGAAAAAAAAAACC[C/T]ACAGCAAGAGGAAGC | 6468 |
rs548804151 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FBXW4 | GRCh38.p7 | 10:101678448 | GTTTGTTTTTTGAGA[C/T]GGAGTCTCGCTCTGT | 6468 |
rs548836893 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101639792 | AAGAGATGAGCACCC[C/T]AGAAGGATAAAGCCA | 6468 |
rs548926784 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | FBXW4 | GRCh38.p7 | 10:101672376 | TTTCTTTTATGCCTT[C/G]GTGGATATCTGTGGA | 6468 |
rs548945698 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101651891 | GTGAGATGAAAGGGG[C/G]CCGCGGCCCTCTCCC | 6468 |
rs548948435 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101615561 | GGAACCCCACTACCT[A/G]GACAAGAAGAAGCAA | 6468 |
rs548951384 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101613697 | TCCCCAACAGAGCTG[C/T]CATCTTCCCGAAGGC | 6468 |
rs549007121 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101655950 | AAAATTCCCCAATCA[A/G]TGAAGAAGCGAGGAA | 6468 |
rs549036814 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101639115 | CCCAAATCATGCAGC[C/T]TGCTAATCATTTTCC | 6468 |
rs549050342 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101657195 | TGTCCTGGCCCAAGA[A/G]AGGAGTAAGAACAAG | 6468 |
rs549074577 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101638773 | TATCTTGGCTCCATC[C/T]GGGACTTGACAGAGA | 6468 |
rs549111844 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101649333 | TGCTTTCTACAATCC[C/G]GGAGCCCCAGCCTAA | 6468 |
rs549113246 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101636618 | TAAAGATGGAGTCTC[A/G]CTCTTGTTGCCCAGG | 6468 |
rs549128560 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101665849 | AATGTTGGGTAGGGA[C/T]GCAGGGCAGAGCCTG | 6468 |
rs549160643 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101641108 | AGTGCTGGGATTACA[A/G]GCATGAGCCACCGCG | 6468 |
rs549182236 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | FBXW4 | GRCh38.p7 | 10:101663316 | TGGGGAAGCTGACAC[A/G]TATCAAGTGTTCAGT | 6468 |
rs549224109 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101624218 | ACAAACACCTTTCCA[C/T]CTTATTTTTGTAACT | 6468 |
rs549287625 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101615169 | TAAGAATGCTTCTCG[A/G]CCTCTCACTGTGGGG | 6468 |
rs549342466 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101655202 | ATTGCCTTACAATGA[A/G]TTCCTAGAAGTGGAA | 6468 |
rs549348809 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101620024 | CCACCATCATCCAGG[A/G]TATAGCAATGCTTAG | 6468 |
rs549402370 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101684347 | TAGCCAGGATAGTCT[C/T]GATCTCCTGACCTTG | 6468 |
rs549425559 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101693963 | GAAAGTCCACAAAAA[C/T]TTATGATAGACCACT | 6468 |
rs549427210 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FBXW4 | GRCh38.p7 | 10:101685591 | GATATAAGAGAACAA[A/G]GTCAGGGCTGCAAAC | 6468 |
rs549439708 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FBXW4 | GRCh38.p7 | 10:101666438 | AAAAAAAATTGAAAG[A/G]GAGTTGTGGAAGGGA | 6468 |
rs549467856 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101683445 | GTTTGCATTCCTGGG[A/C]ATATGACCTATTTTA | 6468 |
rs549470823 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | FBXW4 | GRCh38.p7 | 10:101613599 | GGGCTTGAGGCAGAC[A/G]AGGCAGCCAGCCACA | 6468 |
rs549513825 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FBXW4 | GRCh38.p7 | 10:101662287 | AACCCACCCGCTTAC[C/T]GAACAGTACACAGTG | 6468 |
rs549514042 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101653065 | CCACCTGACTGTCCC[A/G]TAAAACAAAATTCAG | 6468 |
rs549622595 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, synonymous-codon | FBXW4 | GRCh38.p7 | 10:101628002 | GTTCGATTTGAATCC[A/G]CGAGATGTCTTCAAC | 6468 |
rs549767003 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101636388 | AAACAAAAACAAAAC[A/C]AAACAACGGAAAAAA | 6468 |
rs549851824 | snp | A/C | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101630359 | GCTTGTGAAACACTG[A/C]TATTATAGCAGCAAA | 6468 |
rs549901596 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101637929 | ATTTTTTACCTATCA[C/G]AGTGGCAAAATTTTT | 6468 |
rs549933030 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | FBXW4 | GRCh38.p7 | 10:101696740 | AGAGATCATTATAAA[G/T]AAATTTACTTATTCA | 6468 |
rs549935168 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101665733 | ATGAGGGCAGACTCT[A/G]TCCTCAACCTCTTTT | 6468 |
rs549944546 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101635625 | AGATTGCTTGAGCCC[A/G]GGAGTTCAAGACAAG | 6468 |
rs549974241 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101653770 | AAAAACAAACAGTCT[C/T]TTGTGTTTCATACTT | 6468 |
rs550027167 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101691078 | GGGCCAGTGAGGTTA[C/T]GTGGCTTCTGGTCAA | 6468 |
rs550090721 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101678461 | GACGGAGTCTCGCTC[G/T]GTCACCCAGGCTGGA | 6468 |
rs550092313 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101690391 | ATATTTCTATTCCAA[C/T]AGGCTTCATAAAATC | 6468 |
rs550096547 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101679068 | CTCCCTCTCTAGAGG[C/T]AACTATGTATTCACT | 6468 |
rs550120184 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | FBXW4 | GRCh38.p7 | 10:101638201 | AGACACTGGAAATAA[A/C]CTACGTGTCCATCAG | 6468 |
rs550193616 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101630022 | ACACACTTTGGCAAG[A/G]GAGGCCACCAGAGCT | 6468 |
rs550217795 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | FBXW4 | GRCh38.p7 | 10:101682351 | AGAGCCACCTACACT[-/A]ACCAGACTACTGCTG | 6468 |
rs550257235 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101630614 | CACAAAAACTCACTC[A/G]GTGAGGGGAAGCCAG | 6468 |
rs550423798 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101694754 | ATTCCTCCTTCTTCC[A/C]ATACTCTCTTCCTTG | 6468 |
rs550482857 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FBXW4 | GRCh38.p7 | 10:101637111 | ACCATGGGCCGGGCA[C/T]GGTGGCTCACATTTG | 6468 |
rs550487659 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101694092 | TGCAAAAACACACAA[G/T]CGAAAGCTGTAGGGA | 6468 |
rs550573868 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | FBXW4 | GRCh38.p7 | 10:101649272 | GTTATGATGTGCCAT[A/T]GCCCTCCCAGCCAGG | 6468 |
rs550598964 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101632466 | TTTTAACGAAGGGTA[C/G]AAGGTCAGCCTAACC | 6468 |
rs550653937 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101611151 | GTCAGAAGCCTCTAG[G/T]GCAAGGTGCCTGAGC | 6468 |
rs550701143 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101686832 | CTTCTAGGCCATTAT[A/G]ATAAAGTCAAACTGC | 6468 |
rs550725651 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101626029 | GGAGATGTTAGGGCA[A/G]GCACTGGCCAAACCA | 6468 |
rs550771005 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101642548 | TGGGACTTCCAAATT[C/T]CAAGCAGCTCTTACT | 6468 |
rs550830305 | snp | C/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101690364 | TCTTTGATTTTTATT[C/G]TTATATTCAGGATAT | 6468 |
rs550893047 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101650151 | GCAGCAAGGTGAGTG[A/G]TAAAGACAGAAGACA | 6468 |
rs550925665 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101686481 | ATGGCAAGAAAGATG[C/T]GGATTTTTGGGGGGC | 6468 |
rs551005040 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101651126 | CCAGTCTCTGAGCCC[C/G]CAGCTCTGTCCCCCA | 6468 |
rs551007102 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101659963 | TCAAAAGGAGGAAGA[C/T]AAGCATGGAAATCTG | 6468 |
rs551030189 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | FBXW4 | GRCh38.p7 | 10:101676200 | GTTGTCCTTCTGATG[A/C]CCCCTTTGTGTTATT | 6468 |
rs551066516 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101651851 | AAGGAAAATCGGCTG[A/G]CCCATTGTCTCTCCT | 6468 |
rs551089428 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101643285 | TGCTGGCCATTGAGC[C/T]TTCAGTTGCCAACTG | 6468 |
rs551092905 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101652670 | AAGGAAAAGAAAATG[C/T]TTATAAATCTCCATG | 6468 |
rs551131985 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101648597 | ATGGACAGAACCAGC[A/G]CCTTGCCTGGACAGA | 6468 |
rs551165440 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101680865 | TTTTACAAAGATATT[C/T]ATAGCTGCAGCTATA | 6468 |
rs551187413 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101626804 | GGCATCTCTTAAGGC[A/C]TATGGCAGGCCTCTG | 6468 |
rs551211085 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101617588 | TCTGTGTGCACACAC[A/C]CCCAGCACCCACCCA | 6468 |
rs551222978 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101690945 | CAATTAAAAAGTTCC[A/G]TTTTACAATTTATTG | 6468 |
rs551227017 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101646986 | GGGTGGGTGGTGGTG[A/G]TTAGGAATGGGGTGC | 6468 |
rs551241623 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101667090 | CAAAAAATTAGCTGG[G/T]CGTGGTGGCAGGTGC | 6468 |
rs551274517 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101670332 | AACTTCTTAGCTTCC[A/G]TGTCCACATGTGTTA | 6468 |
rs551318509 | snp | A/C | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101624279 | GAAAGTTAAAAAAAA[A/C]AAAAAAACCAGAATG | 6468 |
rs551337519 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101621455 | ACCATTTGAGCCCAG[G/T]AGTTCAAGGCTGCGG | 6468 |
rs551342923 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101659039 | CCCCAAGCCGAAGCA[C/G]GCTATAGAGATCAGT | 6468 |
rs551347156 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101663098 | AGGCTAGGGAACTGG[A/G]TACAAACTACTCCTC | 6468 |
rs551434020 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101646501 | TGGGCTCCAGAAAGC[A/G]TTTCCCCCACAGGAG | 6468 |
rs551476268 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101624125 | ACACACACACAGAGT[G/T]CAATCTGAATAAAGG | 6468 |
rs551492879 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101679831 | ACTTTTAGTATGCCA[A/G]TCACCTGAATAGCGT | 6468 |
rs551494729 | in-del | -/TA | 0.00874735 | 0.0655527 | intron-variant | FBXW4 | GRCh38.p7 | 10:101663715 | GACCTCAGGAGGTTG[-/TA]TCTCTGAGGCCTGTG | 6468 |
rs551508286 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101656204 | CTAGCTCAGCAGCTA[A/G]AAAGAAACCAGTCTG | 6468 |
rs551508882 | snp | C/T | 1.70641e-05 | 0.00292092 | intron-variant | FBXW4 | GRCh38.p7 | 10:101673073 | AATAAGGAGCCGACC[C/T]CCAAGAACCAATTAT | 6468 |
rs551539482 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101615079 | TGTTCTTATAAAAAC[A/G]ATTAGATTGCAATTT | 6468 |
rs551563609 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101638934 | GATGCTATGCGTCAT[A/G]AATTATACACAGTAG | 6468 |
rs551606334 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101612177 | CACTGGGACCAGGGC[G/T]GCCCAAATGTAGGAA | 6468 |
rs551624810 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101631551 | TAAGCAATTCTTTCT[C/T]CTTTTAAATTTTCTT | 6468 |
rs551626571 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101670046 | AGGTGTGAGCCACCG[C/T]GCCCGGCCGGGAGTG | 6468 |
rs551626778 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101639632 | ATCAAGAGATGCGCA[A/G]CTGACCCAAAACTGG | 6468 |
rs551720418 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101690778 | AAGTCCACAGGTTCT[C/G]CTGTCATGTTTCCAA | 6468 |
rs551800157 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101692670 | TGAGGCAGGAGAACC[A/G]CTTGAACCCAGGAGG | 6468 |
rs551805619 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101652412 | ACAACTGGGATCCAC[A/G]ATATTCCCTCACTTT | 6468 |
rs551840071 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101673979 | ACTGGCTACCTAGAC[A/T]TCTCATGGGTACGCA | 6468 |
rs551869247 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101615489 | GACACAGGCTGAGGA[A/G]GGGCAACCTGGGGGA | 6468 |
rs551884834 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | FBXW4 | GRCh38.p7 | 10:101687272 | TAATACCCCCTTCGG[A/T]CTGCTCCCAACAGCT | 6468 |
rs551900850 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | FBXW4 | GRCh38.p7 | 10:101685983 | TAAATTCTTATTCTA[G/T]AGAGGCTCAAGGGAA | 6468 |
rs551959564 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FBXW4 | GRCh38.p7 | 10:101642381 | CATAGCGGGACCCTA[C/T]CTCTATTTTTTTTTT | 6468 |
rs552011746 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | FBXW4 | GRCh38.p7 | 10:101617955 | GGAGGTACTTTAAAG[-/A]GGGGCAGTTCCCGTA | 6468 |
rs552016663 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101634544 | ATATTCATGCTGAAA[C/T]AGGTGAATAGATCAG | 6468 |
rs552020984 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101643263 | TAGCCCAGGCCCAGT[A/T]GGTGGCTGCTGGCCA | 6468 |
rs552049199 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | FBXW4 | GRCh38.p7 | 10:101622585 | TACAAAAAATTAGCC[A/T]GGTGTGGTGGCAGGT | 6468 |
rs552049523 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101656697 | TGCTGTGGGAAGGAG[C/T]GGAGGAAGAGGCAGC | 6468 |
rs552082420 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101622985 | CAATCCAGCAGGCAA[A/C]AGACATGAACAGACG | 6468 |
rs552084079 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101693490 | CAGTAAGATAGCAAT[C/T]ATATGTGCAACTGAA | 6468 |
rs552108613 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101659710 | TTTCTTCTGAATACA[C/T]AGATCTGGGAGAATA | 6468 |
rs552137701 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101627920 | GTGCATCACAGGCAG[C/T]CTCACTGGCCTCAGT | 6468 |
rs552199451 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | FBXW4 | GRCh38.p7 | 10:101696671 | AAGGCAGTGGTTTAT[C/T]GAAAGCACTATTTTA | 6468 |
rs552262710 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | FBXW4 | GRCh38.p7 | 10:101695736 | AGTGCAAGTGGATTC[C/T]CCAAGGACTCAGCAT | 6468 |
rs552289612 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101645245 | GCCCTGACACCCCTG[C/T]GGCATGGAACAGCCT | 6468 |
rs552302711 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101660264 | TCCCTTTGAACCTCC[A/G]ACTGCAACACAGATT | 6468 |
rs552368129 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101661208 | GCTCTTGACAAGTGG[A/G]CCAATCGTGCTGGCC | 6468 |
rs552410374 | in-del | -/TGAA | 0.0023933 | 0.0345097 | intron-variant | FBXW4 | GRCh38.p7 | 10:101629832 | CAAATGCTTATTGAT[-/TGAA]TGAATGAATGAATGA | 6468 |
rs552421503 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101677327 | GTTCATATAATGGAA[A/T]ACTACTCAGCAAAAA | 6468 |
rs552501885 | snp | A/G | | | intron-variant, downstream-variant-500B | FBXW4 | GRCh38.p7 | 10:101625140 | GAGAGCGAGCCTGTC[A/G]GGCTCCTGTTTAGGA | 6468 |
rs552609671 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101636608 | TTTTTTTTTTTAAAG[A/G]TGGAGTCTCGCTCTT | 6468 |
rs552633325 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | FBXW4 | GRCh38.p7 | 10:101653654 | ATTTCCTGTCAATAA[C/T]CCCAGTAGTTGCTAG | 6468 |
rs552672337 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101637012 | TGTGTAGGGATTAAT[A/G]GAGCAAGGTTAGCCA | 6468 |
rs552677504 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101614084 | CAGGCCAGAGCCCTG[C/T]AGGGGAGTCATTCTC | 6468 |
rs552694734 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101631688 | GCTGGAGTGCAGTGG[C/T]GCAATCTCGGCTCAC | 6468 |
rs552739040 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101690187 | ATCAGAATTTGCAGA[C/T]AGCGCTCCTGTTCTT | 6468 |
rs552780826 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101610837 | ATGAACCCCCAGCCC[C/T]GAGAGGTTGGTCAAG | 6468 |
rs552810541 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101653006 | ACATCTCAACCCCAC[A/G]TGTGAGTTCCAGGCA | 6468 |
rs552920225 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101691651 | AAATAAACATCAATT[C/T]TTTCATTCATTCACT | 6468 |
rs552953935 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101682720 | TTTGATCATAGCACC[A/G]AGAAACTTTCAAAGT | 6468 |
rs552973100 | snp | A/C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101688725 | CTCAACCTTGACTCA[A/C/T]GGTTGACACACCTGA | 6468 |
rs552982806 | snp | A/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101648978 | TACCATGCTCCAAAC[A/T]CTGCTTTAAATCCCT | 6468 |
rs553031015 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101640989 | GCACCCGCCACCACA[C/T]CCAGCTAATTTTTGT | 6468 |
rs553059571 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101624321 | GATGGGAATATGTCA[A/G]GCCTGCCAAGGCAGA | 6468 |
rs553094594 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101641708 | TTTTTTTTTAATGAA[A/C]CTGGCCCCAGATCAG | 6468 |
rs553100478 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | FBXW4 | GRCh38.p7 | 10:101684268 | AGCTGGGACTACAGG[C/T]GCCCGCCACCATGCC | 6468 |
rs553104052 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101672799 | GTCCTTTATTGTGTC[A/G]TTTTCTCCCCTGTCC | 6468 |
rs553131094 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101683578 | AATGACCTTTCATTT[C/T]CCCTCTCCTTGCTCA | 6468 |
rs553141385 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | FBXW4 | GRCh38.p7 | 10:101615197 | GGGGGCGAGAGGGGG[G/T]TGCAGAGCCTTGGCT | 6468 |
rs553151122 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101655347 | CAAAGAAGGATTTTC[C/T]GGACCAAAGACTTCT | 6468 |
rs553232317 | in-del | -/T | 0.212425 | 0.24716 | intron-variant | FBXW4 | GRCh38.p7 | 10:101629291 | AGGTACCACTTTCCC[-/T]TTTTTTTTTTTGAGA | 6468 |
rs553271691 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101631150 | AATAAAAAGAAGTTT[C/T]ATTTCACACAGCAAC | 6468 |
rs553279557 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101638516 | AAAAGAGTAGGATAA[C/T]GGGAGGGGACACAGG | 6468 |
rs553281120 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, synonymous-codon, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101694431 | CGAGGCCCGGGCTAT[C/G]CGGCGCCAGAGCAGA | 6468 |
rs553285856 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | FBXW4 | GRCh38.p7 | 10:101637347 | CAGTGAGCCGAGATC[A/G]TGCCACTGCACTCCA | 6468 |
rs553307131 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101652352 | TTTTCTTGATTCTAA[A/G]TCAGTCTCTCTTGCT | 6468 |
rs553341144 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101639222 | GGTGCTAGGCCACTG[C/T]TCATTCATACAACCT | 6468 |
rs553345670 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101649564 | AAATGTCCTCTGAAA[C/G]AGAGTGACCCAAAGC | 6468 |
rs553356860 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101618187 | TGATACTCACTCATA[C/T]CCTGTGCTCAGTTCA | 6468 |
rs553377843 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101656649 | TATGCCATGACTACC[A/G]TGGCCATTGTTCTAA | 6468 |
rs553506462 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101653187 | TGATTTTTTCCTACA[C/T]AGTTTTCCTGAATGA | 6468 |
rs553550205 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101619531 | AGGCGCGGTGGCAGG[C/G]ACCTGTAGTCCCAGC | 6468 |
rs553631442 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101665274 | ACACAAACTATTTTT[C/T]AAAAGACTCCAAGAC | 6468 |
rs553693097 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101666098 | TTTTAAAAGGGCAGC[A/T]TTAGGAAGAAACTGA | 6468 |
rs553714565 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101670495 | TCCCTTCTAAGCCAG[A/T]TGTGATCTGATCTCT | 6468 |
rs553747401 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101680130 | TAATAAATGCTGTTG[A/G]TAAAACTTGTTGAAT | 6468 |
rs553810494 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101678931 | ACTTATTTATTCATA[C/T]AGAATAATTATTTTT | 6468 |
rs553825169 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101661927 | CCTCGAGTTATCAAG[A/G]TCAAGCATCCCCTTT | 6468 |
rs553911024 | in-del | -/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101620648 | TTGTTCTGTTTTTAA[-/T]TTTTTTTTGATAAGA | 6468 |
rs553964343 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101663547 | CTGTAATCTCAGAAC[C/T]TCAGAAGGCCAAGGT | 6468 |
rs554042173 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101666512 | CTGAAGGGCCTAAAC[A/G]AAGTGGGTAGGACCA | 6468 |
rs554125153 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101621876 | AAGGTTTTCAGATAT[A/T]TAAAAGTCTGTTCTT | 6468 |
rs554164168 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101662688 | ACCTTTTTTTTCTTG[A/G]AGGGCAATACATATG | 6468 |
rs554193808 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101621168 | AGAGCCTTCCCTGTG[C/T]CAGGAGTTCAGCAGG | 6468 |
rs554229289 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101654104 | CCAGACCGGCGACAG[A/T]GCGAGACTCCGTCTT | 6468 |
rs554231249 | snp | A/C | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101655071 | TTGGGTTCAAGTGAA[A/C]CTCCTACCTCAGCCT | 6468 |
rs554258612 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101613097 | AGCCCGGGGCTAGCA[C/T]GCCTCCGTGATCACA | 6468 |
rs554346257 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101629472 | TATTTTTAGTAGAGA[A/G]AGGGTTTCCCCAGGT | 6468 |
rs554351642 | in-del | -/AAA | 0.0023933 | 0.0345097 | intron-variant | FBXW4 | GRCh38.p7 | 10:101619659 | GCAAGACTCTGTCTC[-/AAA]AAAAAAAAAAAAGAA | 6468 |
rs554361492 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | FBXW4 | GRCh38.p7 | 10:101657387 | CCTGTAATCCCAACA[C/T]TTTGGGAGGCCAAGG | 6468 |
rs554413102 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101675577 | TGCCAGTGAAACCAG[C/T]GCAAACTGGATGCAA | 6468 |
rs554440118 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101636841 | TGATCCACCTGCTTC[A/G]GCCTCCCAAAGTGCT | 6468 |
rs554455897 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101625724 | AGAGGGGAAGCCTTC[A/G]GGAAACCTGGGCTTG | 6468 |
rs554481037 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101670533 | CTACACTTTCTGGCT[C/T]TTGCCCTAGAGCTTT | 6468 |
rs554604097 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101616262 | AGGTATAAGCTGGGC[C/T]CAACATGGCTGCAAA | 6468 |
rs554605788 | snp | G/T | 0.00199253 | 0.0315007 | intron-variant, synonymous-codon, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101694397 | GGTCGGTGCCGAGCC[G/T]CGTGAAGCCGGAGTT | 6468 |
rs554653170 | snp | A/C | 0.00119737 | 0.0244387 | utr-variant-5-prime, upstream-variant-2KB | FBXW4 | GRCh38.p7 | 10:101695247 | CCTCACACCTGCAGC[A/C]TTGGAGCCACTTCGG | 6468 |
rs554759169 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101640948 | CAATTCTTCTGCCTC[A/G]GCCTCCCGAGTAGCT | 6468 |
rs554800453 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, missense | FBXW4 | GRCh38.p7 | 10:101628027 | TTCAACCAGATTCTC[G/T]TCACATCCCTCACGG | 6468 |
rs554820476 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101632539 | GAGGTTTCTGATTCA[C/T]TCAAGAATCAGAAAC | 6468 |
rs554856441 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101644454 | ACTTGTACTTAGCAC[C/T]ACAGCCCTGCATTTA | 6468 |
rs554859664 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101688482 | ATGAAGAAATGACTC[A/G]AAATTGAGACAAGGC | 6468 |
rs554878449 | snp | C/G | 3.29821e-05 | 0.00406078 | intron-variant | FBXW4 | GRCh38.p7 | 10:101624819 | AAAAGAGCTGCCAAA[C/G]AAAAGGAGAACAAAG | 6468 |
rs554951859 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101634864 | AAAATTCTGAAGCCA[C/T]GAAGGTAGTGATCAG | 6468 |
rs554990034 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101662737 | GGAGCTGTGGGCGCC[C/T]CTCCCTTCCCCTCCC | 6468 |
rs555080291 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101638283 | CAGTCAAAAAGAACA[C/T]GGTAGGATGGGGTGC | 6468 |
rs555227523 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101662629 | CACACTCTCTCACAC[A/G]ATAGCAAGTGTCCTT | 6468 |
rs555261477 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101687537 | CTATTTCTCCCCTAA[C/T]ATGTAACTATTAAAA | 6468 |
rs555266897 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | FBXW4 | GRCh38.p7 | 10:101695933 | CACCAGATTTTGAAG[C/T]CATACAAAAAAAAGA | 6468 |
rs555281471 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | FBXW4 | GRCh38.p7 | 10:101641996 | ACATGGTGAAACCCC[A/G]TCTCTACTAAAATTA | 6468 |
rs555281532 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101651247 | AACACCCTGGCTTCA[C/T]TGTGCCCCAGAAAGA | 6468 |
rs555296937 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101655599 | CACCCTAATCACTCA[C/T]TTGTTCTCTTCTCAT | 6468 |
rs555342988 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FBXW4 | GRCh38.p7 | 10:101642655 | AGGCACCAAATTCTA[C/T]CTCTGAAGCCTCCTT | 6468 |
rs555353384 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101633258 | CTAGCAATCCCATTA[C/T]TGGGTATATACCCAA | 6468 |
rs555358112 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101647782 | TAATGGCTGGGTGAC[C/T]CATCTTACTTCAGGC | 6468 |
rs555425700 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101648571 | TTCATTATCTCAGTC[A/G]ATAATCTTTCATGGA | 6468 |
rs555432025 | snp | G/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101639847 | AGCTAGTCCCAAGGG[G/T]GTATTTCAGTTCTGC | 6468 |
rs555452749 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101629965 | GGCTGGCCTAGAGCC[A/G]CCCAGCTGGCCCAGG | 6468 |
rs555474880 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101631659 | TTGAGACAGAGTCTC[A/G]CTCTGTCGCCTAGGC | 6468 |
rs555493700 | snp | C/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101642803 | ACTGGGGCCAGGGCA[C/G]TGCCTGAATCAATGC | 6468 |
rs555600628 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101613861 | TGCTACCAGCCTCCT[C/T]AGGGAAGTTCTGGTC | 6468 |
rs555622344 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101654007 | GCATCTGTAATCCCA[G/T]CTACTTGGGAGGCTG | 6468 |
rs555657331 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | FBXW4 | GRCh38.p7 | 10:101691600 | TTGCTACAGAATGTA[G/T]ATTCATTCCCAATAT | 6468 |
rs555663424 | in-del | -/CA | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101612823 | ATTCACATGCACATG[-/CA]CACACACACACACAC | 6468 |
rs555681797 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101637350 | TGAGCCGAGATCGTG[C/T]CACTGCACTCCAGCC | 6468 |
rs555683223 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | FBXW4 | GRCh38.p7 | 10:101645749 | GAATTCATTTTTTTT[A/T]AAGTTGGAAACAATT | 6468 |
rs555690190 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101665218 | GGCAGAGATAACACC[A/G]GCATACACTCTGGTC | 6468 |
rs555699173 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101659520 | ACTAAGCCCTCAGAG[C/G]TTATGAAGCAATGAG | 6468 |
rs555714886 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101672646 | AGGGAGGAAAGGCTG[C/T]CAGGTCCTCTGTTTT | 6468 |
rs555823618 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101652206 | GGACTTGAAAGTTTT[C/T]AGTTATATCTCTTTA | 6468 |
rs555859926 | snp | G/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101676265 | CCCCATTAGCCTCTA[G/T]GTAGGACCAGATTTT | 6468 |
rs555867843 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | FBXW4 | GRCh38.p7 | 10:101610182 | AGAATCGCTTCAACC[C/T]GGGAGGCGGAGGTTG | 6468 |
rs555896834 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101672125 | TTTCCTGTTAGCACT[A/G]TGGAACCTAGATGCT | 6468 |
rs556008620 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101636255 | TACTCAGGAGGCTGA[A/G]ACAGGAGAATTGCTT | 6468 |
rs556014986 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101675790 | TTGGTAGCATTAGCA[C/G]TGCCACAGGCATTTT | 6468 |
rs556169612 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101662199 | TCAACAGGCCGCTGA[A/G]TATGCATCTACCACA | 6468 |
rs556171330 | snp | A/C/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101685780 | TGTCTTTAACACAAA[A/C/G]AGTGAGAACCATGGT | 6468 |
rs556210078 | in-del | -/GACCA | 0.00279162 | 0.0372561 | intron-variant | FBXW4 | GRCh38.p7 | 10:101686721 | GTTCTCAACCCAAGT[-/GACCA]GACTTCAAAATCCCT | 6468 |
rs556267949 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101643514 | CCCAGGATGCCGCAG[A/G]CATATGCACGCTTTG | 6468 |
rs556350666 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101671059 | TCAGGTGTATTAGAA[A/G]CCTGGAGAAGCAGCT | 6468 |
rs556470536 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101678727 | GCCACCGCGCCCGGC[A/G]AGATACACTCATTTA | 6468 |
rs556489203 | in-del | -/AC | 0.00119737 | 0.0244387 | intron-variant | FBXW4 | GRCh38.p7 | 10:101667384 | GTTACTACTTCACAT[-/AC]ATGTCTTTGTTTGAG | 6468 |
rs556492331 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101644516 | TGAACCTGAGCAGCC[A/G]TGGGCCAAGGGAGGT | 6468 |
rs556530245 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101693069 | GTGAAACAAACACAT[G/T]GGAATATATTTATCC | 6468 |
rs556578828 | snp | C/T | 8.38314e-05 | 0.00647369 | synonymous-codon, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101611393 | GCTGCTGAGGGGAGT[C/T]GACGTCAGCGGGAAG | 6468 |
rs556593251 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101692468 | AACTATTAAAAAATT[A/T]AATTAGGCCAGGCGC | 6468 |
rs556654598 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101620958 | ACCAAGGCAACCATA[A/G]GCAGAAGAGGCCATT | 6468 |
rs556689553 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101662035 | GAAGTACTCAGCGAG[C/T]TATGAAGTCCAGGGC | 6468 |
rs556737249 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101615329 | TTCCCTTCCAACTCC[C/T]GTGGACAAAGCCCAG | 6468 |
rs556862102 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101617037 | TTTGTGTCTGCTGGA[A/G]CCAGATGAGACGGCT | 6468 |
rs556928706 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101629370 | GCTCATGCAACCTCT[A/C]TCTCCCAGGTTCATG | 6468 |
rs556991320 | snp | A/C | 1.64746e-05 | 0.00287002 | intron-variant | FBXW4 | GRCh38.p7 | 10:101624732 | AGCCAGCATGGGCTC[A/C]TGAATCTCTTACCTG | 6468 |
rs557005127 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101633744 | TATACCAGCAATAAC[A/C]AAGTGTTATTATATA | 6468 |
rs557021025 | in-del | -/G | 0.00636936 | 0.0560724 | intron-variant | FBXW4 | GRCh38.p7 | 10:101642141 | ATTGCACTCCAGCTT[-/G]GGCAACAGAGTGAGA | 6468 |
rs557066741 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101626498 | ACAGACACAGGCATC[C/T]CTTTTTTTTTTGAGA | 6468 |
rs557089394 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101665503 | GGGAAGAAAACATAA[G/T]GCCTAGGTCTTCACC | 6468 |
rs557192707 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101639980 | GTCCTGAGTAATATA[C/G]AGCCTCTGTTCAGTA | 6468 |
rs557225276 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, utr-variant-5-prime, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101694972 | CCTTGCCCCGCTCTC[A/G]CTTTTCCCTTCCCCT | 6468 |
rs557265260 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101631772 | AGCTGGGAATATAGG[C/T]GCATGCCACCACGCC | 6468 |
rs557281678 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101643167 | ACTGCTGAGTCTCCA[C/T]ACCTCACCTCATCCA | 6468 |
rs557300473 | snp | C/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101627638 | CACATGCAATCTCAG[C/G]GTACAACAGATACAA | 6468 |
rs557358288 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101649701 | ATTCCCAAGACAGTC[C/T]GAAGGATGCCAACAG | 6468 |
rs557367509 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FBXW4 | GRCh38.p7 | 10:101646485 | TCTCAGAGGAGATCC[C/T]TGGGCTCCAGAAAGC | 6468 |
rs557403635 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | FBXW4 | GRCh38.p7 | 10:101683671 | AGGGGAAGTGTAGGT[A/C]TATCGAAGAGGTCTT | 6468 |
rs557410525 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101637302 | GAGGCTGAGGCAGGA[A/G]AATGGTGTGAACCTG | 6468 |
rs557413118 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101641082 | GTGATCCACCCACCT[C/T]GGCCTCCCAAAGTGC | 6468 |
rs557452832 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101657813 | CTGCTGATGCATGTA[C/T]TCTTTATTGTCATCA | 6468 |
rs557466773 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101613689 | CTCCCTTCTCCCCAA[C/T]AGAGCTGCCATCTTC | 6468 |
rs557470054 | in-del | -/TTGTTTGA | 0.00159617 | 0.0282053 | intron-variant | FBXW4 | GRCh38.p7 | 10:101667392 | TTCACATACATGTCT[-/TTGTTTGA]GGACCCAGCTGGATC | 6468 |
rs557471982 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101630193 | TGACAGGCACTGACA[C/T]GAGATACAAAGGCAG | 6468 |
rs557504107 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FBXW4 | GRCh38.p7 | 10:101661174 | CTCTGCTTCTACTTG[C/T]AGGGTTTCATGTAAG | 6468 |
rs557550430 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101666239 | TTTGTTTTGAACAGC[A/G]ACAGGTTTATAGGTT | 6468 |
rs557581417 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101686200 | AGTATGTGTGTTCTG[C/T]AAGATGTTAAAGAGA | 6468 |
rs557583063 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | FBXW4 | GRCh38.p7 | 10:101695883 | TTTGAAATGTGGCTA[A/G]TACAAATTGAAATGA | 6468 |
rs557642249 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | FBXW4 | GRCh38.p7 | 10:101695146 | CGGAGCCCAGCCCGA[A/G]CCGCCACCGCCGCCG | 6468 |
rs557649776 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101672821 | CCCCTGTCCCCAGAC[A/G]ATACTCTCAGCCAAT | 6468 |
rs557690018 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101663657 | AAAAAAAAAGAGTCT[G/T]CCCTTCTGTGTTACT | 6468 |
rs557935393 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101681274 | GCGTCTGCAATCCCA[C/G]CTACTCGGGAGGCTA | 6468 |
rs557965914 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101646159 | GAACCTATACTGTTC[C/T]CCTGCAGTATGGGGT | 6468 |
rs558008189 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101661954 | CTTTACACCCAGCTG[C/T]CCACAGCCAGCCAGA | 6468 |
rs558018614 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | FBXW4 | GRCh38.p7 | 10:101653234 | GTCCCTACGAGTCTG[G/T]TCCCTTCCTGCTAAC | 6468 |
rs558036636 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101613421 | CTCCAGGCCTGATGC[C/T]TTAGCTTCCTTTACC | 6468 |
rs558070267 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101662565 | TCCCTAATGACAGAA[C/G]CGGGAGAGAAGGGAT | 6468 |
rs558079978 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FBXW4 | GRCh38.p7 | 10:101644801 | CTGAGCTGCCCATAG[C/T]ACAGGCCACTGCTCT | 6468 |
rs558094115 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101672479 | CTCTCCAGAGAAGCA[A/G]TGAAAACACATTTTA | 6468 |
rs558124826 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101613740 | AGGAGGAGACTGGGG[A/G]TTCCTTTCTGCCCCT | 6468 |
rs558154717 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101667383 | TGTTACTACTTCACA[C/T]ACATGTCTTTGTTTG | 6468 |
rs558197880 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101613170 | CCCCACCCGGGGGCC[A/G]AGAGCAGATTACTGA | 6468 |
rs558257223 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101618028 | AGAGGGCCAGGGCAG[A/G]CAAAGCCACACCTGG | 6468 |
rs558263807 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101643001 | CATCCTCCCCAAATA[A/G]TATAAAATAAGGTCA | 6468 |
rs558299779 | snp | C/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101691318 | AGTCTCTGCAGCTGT[C/G]CAGAAACGGACCACA | 6468 |
rs558336008 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101621214 | ACTAGTCACTAAGAC[A/G]CGGATATTTTAAGAA | 6468 |
rs558336365 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FBXW4 | GRCh38.p7 | 10:101633702 | AACCAAGTGTTATTA[C/T]ATACCAGCAATAACC | 6468 |
rs558338434 | snp | G/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101688133 | CAAATGTCTTTTCCA[G/T]CTCTAACTCCTATGA | 6468 |
rs558459936 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101676675 | ATCTAATGGAGAATG[C/T]ATGACAATCCTGGAA | 6468 |
rs558477269 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | FBXW4 | GRCh38.p7 | 10:101625514 | ACACGAGAAGGAGCA[C/G]GCTGACCCTGTTGCC | 6468 |
rs558519219 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | FBXW4 | GRCh38.p7 | 10:101696930 | TTTAGATTTGTGTTA[A/G]AGATGTTTGTAATTT | 6468 |
rs558570763 | snp | A/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101622089 | GAAAAAAACCATGAT[A/T]CATTGATTAAAACAT | 6468 |
rs558621775 | in-del | -/AC | 0.00199481 | 0.0315187 | intron-variant | FBXW4 | GRCh38.p7 | 10:101692128 | AGAAGTGTAGAAGTG[-/AC]ACACACACATAAATC | 6468 |
rs558645635 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101694911 | CCCGGCTGCCTCCTT[C/T]GCCGTCTGCGGCCCG | 6468 |
rs558655377 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | FBXW4 | GRCh38.p7 | 10:101610488 | TCCATACCCCAAAGG[A/G]TAAGGGATAGGTCAT | 6468 |
rs558688746 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FBXW4 | GRCh38.p7 | 10:101649786 | CCACCTCATCTCAGC[A/G]GCCAGCCTGCATCTC | 6468 |
rs558780147 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101626365 | TTAGGGTAATCCATT[A/T]ATAACTGGTAAAGCC | 6468 |
rs558884908 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101678649 | TAGCCAGGATGGTCT[C/T]GATCTCCTGACCTCG | 6468 |
rs558917002 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101628254 | AAAATTCAAACGGCT[C/T]TTGCCCTCAGTCCCA | 6468 |
rs558976552 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101619608 | AGTTTGCAGTGAGCC[A/G]AGATAGCACCACTGT | 6468 |
rs558989759 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101613534 | CTGGCATGGAGTGAG[A/G]GGACTTCATGGCTCA | 6468 |
rs559071989 | snp | G/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101659131 | TCGGCCCGTGTCCCA[G/T]ATTAATCACCACCAG | 6468 |
rs559093192 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101668519 | GGTGGTGTGTTGTTG[C/T]TTGTTTGTTGATAAT | 6468 |
rs559135700 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101690842 | AGTGCGTGTGTGTGC[A/G]TGTTCTTCCCTTTGT | 6468 |
rs559168868 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101677864 | AATATAAATTCACTG[A/T]ATATATTTTTTTCTT | 6468 |
rs559183854 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101664005 | TCCTTTGGAGCCTGC[C/T]GGTTCTCCTTCTGTG | 6468 |
rs559226183 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101655656 | TTCTCTAGGACAGCT[A/G]AAGCTGCAGCTGCAA | 6468 |
rs559270248 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101643451 | TTTGCTGAGAAGGCA[C/T]ACACACACATACATG | 6468 |
rs559335075 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101635928 | CCCTGGGGGGGCGGG[C/T]GGAGGGAAGAGCGAT | 6468 |
rs559337358 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101663022 | CATCCAAGATGCTGG[C/T]GAATAAGGCACAGCA | 6468 |
rs559366694 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101630461 | ACCTCTGTCCCTCCA[C/T]TGGCTCAGCCAGCAA | 6468 |
rs559367005 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101671145 | TGAATACAATAGTAA[C/T]GTAGAAATGGCTCAG | 6468 |
rs559402289 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101632216 | ACATATTCTCTACAC[A/C]CACACACACACACGC | 6468 |
rs559429568 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101621405 | TGGTGGGGCATGTCT[A/G]TAGTCCTAACTACTT | 6468 |
rs559440933 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101678016 | GCCAAATATTAATTG[C/T]AGAACCTAGGTGGTG | 6468 |
rs559504863 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101631834 | GGGTTTCGCCGTGTT[A/G]GCCAGGATGGTCTTG | 6468 |
rs559549430 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101646912 | TTCTGAGATTTAAAG[C/T]CCCAGTGGAGCCGGA | 6468 |
rs559573728 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101624075 | GCAAAGGACTAGACA[C/T]ACATAGACACAGACA | 6468 |
rs559606373 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101637569 | AAAAATTAGCCAGGT[A/G]TGGTGGTGCATGCCT | 6468 |
rs559610658 | snp | A/G | 0 | 0 | intron-variant | FBXW4 | GRCh38.p7 | 10:101638859 | GAATTCCAGTTTTCC[A/G]GCAGCTCTGACAGTG | 6468 |
rs559747523 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101683121 | GAACAAGGCAGCAGA[A/G]GAAAAGTACCTGAGA | 6468 |
rs559838328 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101624992 | GAGCACTGTGAGGGG[C/T]GTAGCCCCCAGTGGT | 6468 |
rs559840851 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | FBXW4 | GRCh38.p7 | 10:101689431 | ACAGGTGTACTGTTT[C/T]ATTTTGAACCTGTAA | 6468 |
rs559885899 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101684192 | GCAATGGCACAATCT[C/T]GGCTCACTGCAACCT | 6468 |
rs559902651 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101677312 | AACACACTAGGGTAG[G/T]TTCATATAATGGAAT | 6468 |
rs559924505 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101655745 | AGAGACAGTGAGTCT[C/T]GTGCTCTGGACTGGA | 6468 |
rs559928447 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101614988 | ACAATAGCCCCAAAC[C/T]TTGGGGGAAAAGGGG | 6468 |
rs559984859 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101647936 | CCTCTGTGGAAAAGC[C/T]AAAGAGCTTAGACCC | 6468 |
rs560002477 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101642321 | TTTGGGAAGCCGAGG[C/T]AGGAGGATTGCTTGA | 6468 |
rs560008345 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FBXW4 | GRCh38.p7 | 10:101651580 | TGCTTGATGAGTTAG[A/G]GACAAAAATGGCCCT | 6468 |
rs560061722 | snp | A/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101655239 | TGTCAAAAGGTTTTC[A/T]TGTTTTAATTTTGAT | 6468 |
rs560077306 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101688952 | CAGGACCAGAAACTA[A/G]TCCAGTGCCAGGGTC | 6468 |
rs560106260 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101635406 | TTGAATCATCCCAAA[C/T]CCTGACTCACCCCCC | 6468 |
rs560118798 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101659769 | TTCCAACAAGGTACA[C/T]GCAGAGCTAGTATGT | 6468 |
rs560259206 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101658802 | CCCCTAGTCTACTTA[C/T]AAGAGTAAGCTCCAT | 6468 |
rs560311374 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101653536 | CCCTTGCTTGAAGTT[C/G]CCTTATGCAATTTCA | 6468 |
rs560353388 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101668856 | AAACAGAAAGGAAAT[C/T]TCAGACGTACAGGAC | 6468 |
rs560414905 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101669828 | GGCGCAATATCAGCT[C/T]ACTGCAAGCTCCGCC | 6468 |
rs560638637 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | FBXW4 | GRCh38.p7 | 10:101619135 | CATAGTTCCTCAGGG[A/C]CTGATGGGATCACAG | 6468 |
rs560670340 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101619869 | ATGGTGACCCTGAAA[A/G]GGGTCCAGGTTCTGT | 6468 |
rs560671144 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FBXW4 | GRCh38.p7 | 10:101683053 | TTTCTCTGAAAACAG[A/G]TATCCCTCCATCCCT | 6468 |
rs560677325 | snp | C/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101651308 | CGCCCAGAGAGAAAA[C/G]AGAGGCCAGTGGGGT | 6468 |
rs560731693 | snp | G/T | 0.000399281 | 0.0141238 | downstream-variant-500B | FBXW4 | GRCh38.p7 | 10:101610647 | TGCTAGGACTACTCA[G/T]CCAGTGAGGAACCAG | 6468 |
rs560791694 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | FBXW4 | GRCh38.p7 | 10:101628458 | CTTTAGAGGCTCTTG[A/G]GTACTGTACTGTCTA | 6468 |
rs560793000 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FBXW4 | GRCh38.p7 | 10:101611503 | CCAGGGGAAGAGGGA[C/T]GTGTGCCATTGTAGG | 6468 |
rs560834448 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101655960 | AATCAATGAAGAAGC[A/G]AGGAAGGAACACTCA | 6468 |
rs560839044 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101661191 | GGGTTTCATGTAAGT[C/T]GGCTCTTGACAAGTG | 6468 |
rs560853473 | snp | A/C | 1.64836e-05 | 0.0028708 | synonymous-codon, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101673637 | AGCCTGGGATATGTA[A/C]AGAGAATCATCCTCT | 6468 |
rs560903814 | in-del | -/TACAA | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101682052 | ACACCTAAAACGAAG[-/TACAA]TACATGTTATAAATC | 6468 |
rs560957096 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101649012 | TGCTCCACAAAGTTA[A/C]CAAGAGCAATTCCTG | 6468 |
rs560966094 | in-del | -/CCT/CCTCCT | 0.0155373 | 0.0867598 | intron-variant, cds-indel, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101694600 | CCGACTCCCGAGCCG[-/CCT/CCTCCT]CCTCCTCCTCCTCCT | 6468 |
rs561092112 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101663711 | ATGTGACCTCAGGAG[A/G]TTGTATCTCTGAGGC | 6468 |
rs561126582 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101626599 | GGTTCAAGCAGTTCC[C/T]CTGCCTCAGCCTCCC | 6468 |
rs561165287 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101666468 | AGTAGGAGGAGGGGT[C/G]CAGGCTCCATGGGGT | 6468 |
rs561198339 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101638043 | TAACTGGAAGGCAAT[A/G]TGGTGGTGTCTAAAA | 6468 |
rs561203537 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101615391 | CCACACCCTAGCCTC[C/T]GCCGAGTCAAGTCCA | 6468 |
rs561238680 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101693990 | CACTTAAGGAACCTG[A/C]GTCCTAGACCTGGAC | 6468 |
rs561357246 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101630280 | CTCCAGTGCTCCTAA[C/T]TGGAGGAAAAATTGC | 6468 |
rs561359373 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101620452 | CTTCTCTGGGGACAG[A/G]ACAGATGTTTAAACA | 6468 |
rs561420895 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101621324 | TTGAGCCAACGAGTT[C/T]GAGACCAGCCTGGGC | 6468 |
rs561433647 | snp | A/C | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101624395 | ATTCTTTTTATAGGT[A/C]CGTAGGCCACCTTCA | 6468 |
rs561471290 | snp | A/C | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101656134 | CTTGGGTATATTTAC[A/C]CTGGAAAAGCTCACC | 6468 |
rs561481447 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101641171 | ATGCCAGGCATTTAA[A/G]AGATAGATAATTTAA | 6468 |
rs561595658 | snp | G/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101628561 | CAAAGCCTACACAGC[G/T]GGGAAAGCTAGTCAT | 6468 |
rs561667998 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101612678 | AACCAGTCCCAGGCC[C/T]CACCCCTCCCCCAGC | 6468 |
rs561694337 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101629727 | ATTATACCACCCCTC[A/G]CCCAGAAGTTCTCAT | 6468 |
rs561780811 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101626630 | GAGTTGCTGGGACTA[C/T]GGGCATGCACCACCA | 6468 |
rs561820085 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101636917 | AAAAAGTATCACTAT[A/C]TTTTAGAGTACAGAC | 6468 |
rs561823119 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101653362 | CAAAACGGTCCAAAG[C/T]TCCCTATTTTCCTCA | 6468 |
rs561875093 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101637371 | CACTCCAGCCTGGGC[A/G]ACAGAGTGAGACTCC | 6468 |
rs561880720 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101644036 | ATTCCCCCCATCCCA[C/T]ATTCGTACCTGGGCT | 6468 |
rs561922611 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101680513 | ATAACACCCTGTCTC[C/T]AATACCATATCATCC | 6468 |
rs561929953 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101682165 | CTCTAATAATCATTC[A/G]TTTTTCTTCTAATTA | 6468 |
rs561941249 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FBXW4 | GRCh38.p7 | 10:101636396 | ACAAAACAAAACAAC[A/G]GAAAAAAAAAAAACA | 6468 |
rs561953445 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101638727 | GCACACTGAATTAAA[C/T]GTGATTCTGATTATT | 6468 |
rs561973623 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101654277 | TGAAAGTGTTAGAAA[G/T]GTTCTCAAATGGAAT | 6468 |
rs561984300 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101679377 | CATAAAGAGCAATTA[C/T]AATTCTTATATTTCT | 6468 |
rs561984486 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101690812 | CATTCAGGACAGGTG[A/T]GAGAAACGAAGCACA | 6468 |
rs562016716 | in-del | -/A | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101663636 | GCAAGACCCTGTCTC[-/A]AAAAAAAAAAAAAAG | 6468 |
rs562018185 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101631380 | ATGTTCCCAAATAAT[A/G]CAAGCAAGAGACTTA | 6468 |
rs562036903 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101654930 | CTGGGCTCAAGCAGT[A/C]CCCCCACCTCAGCCT | 6468 |
rs562110178 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101662923 | ATATGCTGCCTTCTC[C/T]CACCACTCCCTGTCT | 6468 |
rs562190208 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101639409 | TATCAGACTCTTCAC[A/T]TTGTTTAAGAGTTGG | 6468 |
rs562226127 | in-del | -/AATA | 0.00199481 | 0.0315187 | utr-variant-3-prime, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101610976 | GGCTGTCATGGCTCT[-/AATA]AATAAGGGGTATAGG | 6468 |
rs562256981 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101631825 | GTAGAGATGGGGTTT[C/T]GCCGTGTTAGCCAGG | 6468 |
rs562324436 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | FBXW4 | GRCh38.p7 | 10:101686863 | ATCCAAGATAAGGGA[A/T]GAAGTTCTCCCTTAG | 6468 |
rs562330195 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101682040 | TTTTTTAAAATGACA[C/T]CTAAAACGAAGTACA | 6468 |
rs562338102 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101663866 | CTCCAGGTGAGACCT[A/C]CTCTACAGGAGAAGG | 6468 |
rs562437832 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101650255 | TTAGGCCCTAGTTCC[C/T]AGGGACATTCCCCTT | 6468 |
rs562451508 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101620620 | GGAAGAACTGAGGCC[A/G]TAGTTGTTTGTTTTG | 6468 |
rs562477193 | snp | A/C | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101627568 | TCATTAGGAAGAATG[A/C]GCAAAAGCTACAGAC | 6468 |
rs562492457 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101635291 | GAAAACAAGCTCAAG[C/G]CTCCCACTGATTCTA | 6468 |
rs562647937 | in-del | -/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101631059 | GAAGATAAACACAAC[-/T]TTTTTTTTTTATCAA | 6468 |
rs562661950 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101687901 | CTCAGCTGAGACCAC[C/T]AACAAAGAAGTCCAT | 6468 |
rs562690407 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101666766 | ACTTGTCCATAGGTA[A/G]AGTTAGAGATATAAC | 6468 |
rs562736316 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | FBXW4 | GRCh38.p7 | 10:101610573 | ATGAGGCTGGTCTTG[C/T]CGTTTCAGCAGCACA | 6468 |
rs562900187 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101660872 | TACCACACTCTACTA[C/G]CTATTTTACTTGTCG | 6468 |
rs563085288 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101627622 | TTAGAAAGGGCGTGC[A/G]CACATGCAATCTCAG | 6468 |
rs563148679 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101618789 | GGTCTGGGATTAAAG[G/T]GCTCTCCATCCTGAA | 6468 |
rs563192293 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101682061 | ACGAAGTACAATACA[C/T]GTTATAAATCACTAC | 6468 |
rs563209573 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101619723 | TGCCATTTAGGCAAC[A/G]GCTGTGTGCCTGTGG | 6468 |
rs563265585 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101672857 | GACTCAGGGATCTAT[C/T]CACCCCCTCCCTATA | 6468 |
rs563301924 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101653226 | TTCCCACTGTCCCTA[C/T]GAGTCTGGTCCCTTC | 6468 |
rs563306974 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101664736 | AAGAAAGGATTCTGG[C/T]TGACATTACATTATA | 6468 |
rs563407686 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101622456 | CAAGCAGCCGGGTGC[A/G]GTGGCTCACGCCTGT | 6468 |
rs563411898 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101625752 | TTGAAACTTAAACAG[C/T]AAGCAAGCAAGTTGA | 6468 |
rs563473096 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101673358 | GGTAAAATCTCTCTG[C/T]TTTAAATGGAAAACC | 6468 |
rs563479852 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101631344 | TCTACTTAATGGAAT[A/G]TTATACAGTCCTTTT | 6468 |
rs563688326 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101648050 | AGGTCACCCAATCAT[C/T]AGGGAGGTCCCTGTC | 6468 |
rs563723209 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101654046 | GAATCACTTGAACCC[C/T]GGAGGCGGAAGTTGC | 6468 |
rs563748274 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | FBXW4 | GRCh38.p7 | 10:101628489 | GCACAGTGCCTGGCC[C/G]AGAGAAGGCACTCAA | 6468 |
rs563748425 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101636837 | CAGGTGATCCACCTG[C/G]TTCGGCCTCCCAAAG | 6468 |
rs563755375 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101639640 | ATGCGCAGCTGACCC[A/C]AAACTGGCCTGGGAT | 6468 |
rs563777776 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101611504 | CAGGGGAAGAGGGAC[A/G]TGTGCCATTGTAGGC | 6468 |
rs563839442 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101616681 | ACCAGGCTGTTTTGG[C/T]GGCAGCTGGCAATCT | 6468 |
rs563900134 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101674771 | GATTCCCTCTGCAAT[A/C]TGACAGGAGGAAGAA | 6468 |
rs563970863 | in-del | -/ATTTT | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101683950 | TGCTTGGGGCTTGGA[-/ATTTT]ATTTTATTTTAATTA | 6468 |
rs563988838 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101684285 | CCCGCCACCATGCCC[A/G]GCTACTTTATTTTTG | 6468 |
rs563995770 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101640537 | CACTCTGTTGCCCAG[C/G]CTGGAGTGCAGTGGC | 6468 |
rs564176815 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101619947 | TAGACGTGGGTGATG[G/T]CTCCCCTGATGGGAG | 6468 |
rs564179765 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101689678 | CCAGTTAGCAATACC[A/G]TCTCCATTCAGGGTT | 6468 |
rs564235563 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101660747 | GAGTGGAAGAAAGAG[C/T]GGTGCAGGTAGGGAC | 6468 |
rs564285813 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101654224 | CAAGCATGAAACCAT[C/G]TTTAATGATACAAAA | 6468 |
rs564319945 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101690947 | ATTAAAAAGTTCCGT[C/T]TTACAATTTATTGTG | 6468 |
rs564330222 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101643264 | AGCCCAGGCCCAGTA[G/T]GTGGCTGCTGGCCAT | 6468 |
rs564347568 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101646073 | TCACTCTTGTCATTA[C/T]TGTGATCATCACTGG | 6468 |
rs564360894 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101678416 | CAGGGAGAGATACAC[G/T]AATTTCTTTTTTGTT | 6468 |
rs564422272 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FBXW4 | GRCh38.p7 | 10:101689030 | AGTCACACATTCAAA[A/G]ATAATTTTTTAAAAA | 6468 |
rs564437950 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101662753 | CTCCCTTCCCCTCCC[A/C]GGCAAACAGGGTATG | 6468 |
rs564514600 | snp | C/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101637790 | GGAAGATGAGGAATA[C/G]AGAGGTAACTCACCA | 6468 |
rs564519374 | snp | A/C | 0.000149456 | 0.00864324 | intron-variant | FBXW4 | GRCh38.p7 | 10:101611607 | CTGGCATGCTGGAGA[A/C]GAGGTGGGCAGGACA | 6468 |
rs564524473 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101682162 | TGACTCTAATAATCA[C/T]TCGTTTTTCTTCTAA | 6468 |
rs564591201 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101646743 | CAAATAAAGCCACAG[A/G]GAGAGGGAGAAGGAT | 6468 |
rs564615971 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101638613 | CATATTTATGTATCA[C/T]TTATGTATAAAACAA | 6468 |
rs564687512 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FBXW4 | GRCh38.p7 | 10:101649238 | TCATCTCTCTCCTCC[A/G]TCAAGTTTGCATTTA | 6468 |
rs564711402 | snp | C/T | 1.87173e-05 | 0.00305913 | intron-variant | FBXW4 | GRCh38.p7 | 10:101673704 | AGAAAATTTAAAAGT[C/T]ATCAAGATACAGTAT | 6468 |
rs564717447 | snp | C/T | 0.00111297 | 0.0235636 | intron-variant, utr-variant-5-prime, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101694682 | CCCAAGCCTGACCCC[C/T]TCGTCCCTGTGCTCT | 6468 |
rs564769485 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101612531 | GGGTCATACACATTC[A/G]TTCCACCTTCAGAAG | 6468 |
rs564819850 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101650902 | CGGGCTCTCGAGAGA[C/T]GCGGCCTGTTGGTCT | 6468 |
rs564836156 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101666394 | TGAAGAATTAATGAC[A/G]TGGCTAATCGGCTCT | 6468 |
rs564858431 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101657525 | TGTAGTACCAGCTAC[C/T]TGGGGGGCTGAGGCA | 6468 |
rs564917269 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101650020 | AGGCTGAGGCTCCCC[A/G]GAGTCTCCTTCTCCT | 6468 |
rs564957816 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101641327 | GGGGTTAATTTTACT[A/G]TTTTTCTCTTTATCT | 6468 |
rs564998950 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101616419 | CCCTGCCTTCAAGGA[A/G]TATTCAATCCAGGGA | 6468 |
rs565040201 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101644665 | GAAAAAGATTCTCCC[A/T]GAAATGCCACAGACC | 6468 |
rs565094325 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101615420 | CAGCAATTCTCTCTC[C/T]ACCCAGGGAAACATA | 6468 |
rs565215754 | snp | C/T | 0.00165 | 0.0286754 | intron-variant | FBXW4 | GRCh38.p7 | 10:101668014 | ATGCTCTCGTTGGCA[C/T]TGCCTGGGATCAGTG | 6468 |
rs565273072 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101676176 | TTCCCTTCTTTAAAA[G/T]GTGAAAAAGTTGTCC | 6468 |
rs565314214 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101658975 | AGTCAGACAGGGCTA[A/C]AAGTTTCCGCTCTAC | 6468 |
rs565314270 | snp | C/T | 3.29598e-05 | 0.00405941 | intron-variant | FBXW4 | GRCh38.p7 | 10:101667861 | TTATACAGGACAAAA[C/T]CACATCCAAATATGT | 6468 |
rs565332131 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101686500 | TTTTTGGGGGGCAGG[A/G]AGCGGTGAACAGGCC | 6468 |
rs565345395 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101625953 | TTTCCACAGAGAGGG[C/T]CCTGGAGAAGCCAGT | 6468 |
rs565375501 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101659820 | CATGTTAGAATACAC[G/T]TTTTAGGACCAAAGG | 6468 |
rs565431278 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101642149 | CCAGCTTGGGCAACA[C/G]AGTGAGACTCTATCT | 6468 |
rs565434326 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101645466 | GGACACCCTCTCCCC[A/G]TCACCTTTTCCTCAG | 6468 |
rs565465955 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101652422 | TCCACGATATTCCCT[C/T]ACTTTGTCACTTACC | 6468 |
rs565481269 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101627322 | AAGCAGAGTGTCTTC[C/T]TGGCACTTAGGAGGA | 6468 |
rs565495493 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101633948 | CTGTCTCTACTAAAA[A/T]ATATATATATATAAA | 6468 |
rs565501737 | snp | A/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101689817 | CTCTGGACGTTAATC[A/T]TCACTGAAATAGATA | 6468 |
rs565513687 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101662442 | AGACTTGGACTAATC[C/T]CCTCAAAAACAAACA | 6468 |
rs565519239 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101646221 | TTCTATTCTGTAGAC[C/T]ACTTTAGAAAGCTAC | 6468 |
rs565521819 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101674159 | ACATGATAAAACCCC[A/G]TCTCTACTAAAAATA | 6468 |
rs565553273 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101626737 | TCGTGATCCGCCCAC[C/T]TTGGCCTCCGAAAGT | 6468 |
rs565575320 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101653858 | CCAGGCGCAGTGGCT[C/G]ACGACTGTAATCCCA | 6468 |
rs565614751 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101617510 | TGGAAGCTTCACTTG[C/T]CTCAGCCCCATCAGG | 6468 |
rs565661154 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101636675 | TCTCTGCAACCTCTG[C/T]CTCCCGGAATCAAGC | 6468 |
rs565678709 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101611951 | AAGCATCTTCTGTAG[A/G]GGGCTCTCGCCATGG | 6468 |
rs565690450 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101628878 | GAAGCCAGCCTTCTA[C/T]AATTTCTCACCCTGT | 6468 |
rs565721407 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101671774 | AATCAGAAGCCTGAA[A/G/T]TAAGTATGAAGTAGG | 6468 |
rs565753063 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101620080 | CGCTCTCTGCCCAAG[C/T]CCCAGCACATACATA | 6468 |
rs565761985 | in-del | -/AG | 0.00318978 | 0.0398085 | intron-variant | FBXW4 | GRCh38.p7 | 10:101618404 | GGTTTCATTAGGCAC[-/AG]AGGGGGTATTCTGGG | 6468 |
rs565795333 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101678589 | CACCACCACACCCAG[C/T]TAATTTTTTTTACTG | 6468 |
rs565824279 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101638974 | AGTAGGATCCATGAC[A/G]ATAAGAGCTACTGTA | 6468 |
rs565891021 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101621917 | GTTCAACTTGCTTGT[C/T]TCTTGTCTAGGATCA | 6468 |
rs565895009 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101637218 | GAAACCCCATCTCTA[C/G]TAAAAATACAAAAAA | 6468 |
rs565895179 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101646484 | TTCTCAGAGGAGATC[C/G]CTGGGCTCCAGAAAG | 6468 |
rs565913144 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101681064 | AAAGGTAGAGGTGGG[A/G]AGACACTACATAAAA | 6468 |
rs565931004 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101669348 | TAGGCAGCCCAGCTA[A/T]AAAGACAGCTTTGCC | 6468 |
rs565943213 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101620580 | GCTGGCCAGAGCGGG[A/C]AGGGCTGTTTCTTCT | 6468 |
rs565979126 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101691170 | CCCAAAGCAATGAAC[G/T]ACAGCCCTGCCACTA | 6468 |
rs565992029 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101670002 | CCTCATGATCCACCC[A/G]CCTCAGCCTCCCAAA | 6468 |
rs566019342 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101631543 | TAGAATGATAAGCAA[C/T]TCTTTCTTCTTTTAA | 6468 |
rs566041897 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101692197 | TATCAAAAAGTAACA[A/G]TATTTAAAATAGTAT | 6468 |
rs566082729 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101622793 | TTGCAAATCACATAT[C/T]TGACAAAGGACTAAT | 6468 |
rs566097611 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101613104 | GGCTAGCACGCCTCC[A/G]TGATCACAGCCCCCA | 6468 |
rs566125194 | snp | G/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101645787 | ATCAACAAGTTCTAA[G/T]TCCAAATGAGAGAGC | 6468 |
rs566158802 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101613725 | GGCCGAAGGAATCAA[A/G]GGAGGAGACTGGGGG | 6468 |
rs566233641 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101630820 | GATGTGATGGGAAGG[A/G]GAAAAAAACAGGCAA | 6468 |
rs566294764 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101650380 | GATTGCAGAGTAGTC[C/T]CTGCAGCTGACCTGT | 6468 |
rs566300352 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101634493 | AAGAACAATAAGAAA[A/G]AAGTTGTTCTACCGG | 6468 |
rs566320949 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | FBXW4 | GRCh38.p7 | 10:101695525 | CATGTGAGGGCCCAA[C/G]GAATCTGCAGCCCTA | 6468 |
rs566329449 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101687451 | TACCCTAATCCAAAA[C/T]ACTTGCTTCCGGCCC | 6468 |
rs566362189 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101626879 | GGGGAGCAACTTTAA[A/T]CCTGCTGGAGATCAG | 6468 |
rs566490383 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FBXW4 | GRCh38.p7 | 10:101617131 | TGTGTACCAGGCAAC[A/G]TGCTGAGTGTTTTAC | 6468 |
rs566503072 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-5-prime, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101694880 | GGCATGCCCTCGCTC[C/G]CGCGTCAGCCCCCGG | 6468 |
rs566552590 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101617951 | GAAGGGAGGTACTTT[A/G]AAGAGGGGCAGTTCC | 6468 |
rs566574192 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101667274 | TTCTAAATATAAAAT[A/G]AAATAAATAATAATA | 6468 |
rs566667171 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101687251 | GCAGAGTTACCAGAA[A/G]AAATATAATACCCCC | 6468 |
rs566752325 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101633466 | GTAGTGGGTTAGGGG[A/C]GGGATAGCATTAGGA | 6468 |
rs566841064 | snp | G/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101656342 | TAAGTGTCTCCAGCC[G/T]GGAACCAGAAAGTCA | 6468 |
rs566888345 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101635856 | AGAAAAAAAAAAAAA[A/G]AGAGAGATGGAGGGG | 6468 |
rs566925465 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101645111 | AAGAACTACTGTCCA[C/T]ACCCTCACCCCCACC | 6468 |
rs566962697 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101636562 | TAATATTTTTCTAGG[G/T]ATGATAATGGTATTA | 6468 |
rs567031573 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101659377 | AAAGATGCAGTGACT[C/T]GTGCAGTAAAGTCCA | 6468 |
rs567153912 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | FBXW4 | GRCh38.p7 | 10:101696811 | TTCACATTTAGGTGA[C/T]GTCATGAGTTCAATA | 6468 |
rs567180949 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | FBXW4 | GRCh38.p7 | 10:101639166 | GCCAGACCTGTGCCA[A/T]CCCAGGACTTGGTTC | 6468 |
rs567234815 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101647264 | CTCTCACCCACAGGT[C/T]GTTCTGCCCCCATCA | 6468 |
rs567342521 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101639800 | AGCACCCCAGAAGGA[G/T]AAAGCCATGGCAGCA | 6468 |
rs567401891 | snp | A/C | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101681389 | GCGAAACTCCGTCTC[A/C]AAAAAAAAAAATAAT | 6468 |
rs567423214 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101649415 | TGTTTCTCTCAGGCT[C/T]TTTATGAGCTGTCCA | 6468 |
rs567428299 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | FBXW4 | GRCh38.p7 | 10:101692886 | ACTGGCAGAGCCTAA[A/T]AAAGTGTAAAACAGT | 6468 |
rs567493059 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101664364 | CTAACTGTCCAGGTT[C/G]CTCCTAACTGCATAA | 6468 |
rs567507515 | snp | G/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101630057 | CATCATTCACCAACA[G/T]GCCCATCAAGTGTAT | 6468 |
rs567567847 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101655246 | AGGTTTTCATGTTTT[A/G]ATTTTGATACTCATT | 6468 |
rs567568045 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101686884 | TCTCCCTTAGCAACT[C/T]ACTTCTGGAGGGGAC | 6468 |
rs567596919 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FBXW4 | GRCh38.p7 | 10:101625093 | CACACCATAAAAACA[A/G]ATCTCTAGACGTGAC | 6468 |
rs567596934 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | FBXW4 | GRCh38.p7 | 10:101615192 | CTGTGGGGGGCGAGA[G/T]GGGGGTGCAGAGCCT | 6468 |
rs567626549 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FBXW4 | GRCh38.p7 | 10:101665898 | AATCCATATGAAGGA[A/G]GCGCACAGACCATCT | 6468 |
rs567632502 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FBXW4 | GRCh38.p7 | 10:101690451 | ACTGACTCCAACTAT[C/T]TTTGTGTCCCTTTAA | 6468 |
rs567654653 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101657822 | CATGTATTCTTTATT[A/G]TCATCATGTGTAAAA | 6468 |
rs567657777 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101615614 | AGAGGTCAGGGCCCC[C/G]TGGCCCAAACCATCC | 6468 |
rs567692359 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101657204 | CCAAGAGAGGAGTAA[A/G]AACAAGCTTGGAAAT | 6468 |
rs567864003 | snp | C/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101620449 | AAGCTTCTCTGGGGA[C/G]AGGACAGATGTTTAA | 6468 |
rs567990632 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101619441 | AGGCAGGTGGATCAC[A/G]AGGTCAGGAGATCGA | 6468 |
rs568000733 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101628795 | AGTACACATATCCCC[G/T]CTTAGCTAGAGGGTC | 6468 |
rs568004799 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101661364 | CCAGGGTCTTGAGGA[A/G]TTGAAACCCACCCCT | 6468 |
rs568022729 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101694049 | GACTGGCTCCTCTGG[A/G]GCGAAGGAACCGGGG | 6468 |
rs568057186 | snp | G/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101631049 | CCAGGCAGGGGAAGA[G/T]AAACACAACTTTTTT | 6468 |
rs568063181 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101620035 | CAGGGTATAGCAATG[C/T]TTAGGGCAAACTGCC | 6468 |
rs568109076 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101689237 | CAGACTGTGAAGACA[C/T]TGGGTTTCTCCATGT | 6468 |
rs568181555 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101657477 | CATCTCTATTAAAAA[C/T]ACAAAAATTAGCTGG | 6468 |
rs568282687 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101644544 | GGTGGCTATGCAGCA[A/G]GGTGGCCACAGTGCT | 6468 |
rs568282769 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101653804 | ATGTGATCTTGCACA[C/G]AGCAGCATTCAATAC | 6468 |
rs568313770 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101630036 | GGGAGGCCACCAGAG[C/T]TGTCACATCATTCAC | 6468 |
rs568359571 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101668299 | GAAGTGGGTGGGTGG[G/T]GCTTGCCTCTTTTGA | 6468 |
rs568362880 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101681018 | ACAACTATAGCAAGT[A/T]ATGGTATTTTTAAAA | 6468 |
rs568395746 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101638005 | TGTACACACTGTTTG[C/T]GGGTATAGAACCTGA | 6468 |
rs568456000 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101630618 | AAAACTCACTCGGTG[A/G]GGGGAAGCCAGGAGC | 6468 |
rs568475869 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101671620 | AGTAAGCCTGAAGCC[A/G]TGACAGGAAGATGGC | 6468 |
rs568484333 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101694181 | TGCTCTCGGGAGGCT[A/G]CCTCAGATGGAGGCC | 6468 |
rs568542097 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101621651 | CTGTATGGGAAACTC[G/T]TTCACGATAATTTTG | 6468 |
rs568606629 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101612983 | AGGGGAGTCCCAGGA[G/T]ATGTTAAAACAAGTA | 6468 |
rs568719573 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101641419 | GATCTTTCTTTGTAA[A/C]CCCAAGCAACTCCTT | 6468 |
rs568723273 | snp | C/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101691470 | GGACACCTTACCCTA[C/G]GACATGGGCGAGAAA | 6468 |
rs568820976 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101684522 | TGATCCACCTGCCTC[A/G]GCCTCCCAAAGTGCT | 6468 |
rs568831849 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | FBXW4 | GRCh38.p7 | 10:101632504 | GGAGAGCCTAGCCCA[C/G]GCTAGACAAAAGGAA | 6468 |
rs568850343 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101656716 | GGAAGAGGCAGCAGG[A/G]CAAGCTAAGCAGGCC | 6468 |
rs568893120 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101633244 | AAATACCATTTGACC[C/T]AGCAATCCCATTACT | 6468 |
rs568895648 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | FBXW4 | GRCh38.p7 | 10:101625404 | CTACATAGGTGGGGC[A/G]GAGTCCCCAGAAGCC | 6468 |
rs568913031 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101660186 | ACAGCACCTTCATTT[A/G]AGGAGTAACACCGAC | 6468 |
rs568924541 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101648513 | TGAGCTCCGGGGCTG[C/T]AGCAGTGGCAACAGG | 6468 |
rs568982624 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101616958 | GCTCCTGGAAATCCC[A/G]TCTGGTAGCAGCTTT | 6468 |
rs569017251 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101675510 | TCTCTCCTGTAGTTT[A/C]TTTACCATCATCACC | 6468 |
rs569068234 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101649304 | CTTGGCAGGGCAGCC[C/T]AGGGAAGTCACAGTG | 6468 |
rs569129965 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101640882 | GTCGCTCAGGCTGGA[C/G]TACAATGGTGTGATC | 6468 |
rs569158956 | snp | C/T | | | intron-variant, downstream-variant-500B | FBXW4 | GRCh38.p7 | 10:101625309 | AATGTGGTATAAGCA[C/T]AGGGCAGGTATAAAG | 6468 |
rs569197128 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FBXW4 | GRCh38.p7 | 10:101630409 | ACCTGGGGGCCCCCC[A/G]ATTTCCCTTGGCCCC | 6468 |
rs569241996 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101651138 | CCCCCAGCTCTGTCC[A/C]CCAGGGATTGTACAG | 6468 |
rs569242950 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101643315 | GTCCAAGGTGGAAAG[C/T]TGTGCTATGGCTCAA | 6468 |
rs569273181 | snp | C/T | 8.26932e-05 | 0.0064296 | missense, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101676414 | ACACCTTCACTCGTT[C/T]CTTCACTGGGACACT | 6468 |
rs569303120 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101651864 | TGGCCCATTGTCTCT[C/G]CTCTGTGCTAAGTGA | 6468 |
rs569314378 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FBXW4 | GRCh38.p7 | 10:101674291 | CCGAGATCGCACCAC[C/T]GCACTCCAGCCTGGG | 6468 |
rs569318081 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FBXW4 | GRCh38.p7 | 10:101655403 | ATTTGTGGTTTTTTT[C/T]CCTATTAATTTTTGT | 6468 |
rs569326541 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | FBXW4 | GRCh38.p7 | 10:101696746 | CATTATAAAGAAATT[G/T]ACTTATTCACAGGTA | 6468 |
rs569393808 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101667123 | GTAGTCCCAGCTACT[C/T]GGGAGGCTGAGGCAG | 6468 |
rs569457161 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101627832 | CACAGGACCTGTTAC[C/T]CCCACACTCAGACTC | 6468 |
rs569483825 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101617672 | GCTAACAAGGGGGCC[A/C]TAATTACAGGAAGGG | 6468 |
rs569542807 | snp | A/G | 0.000798403 | 0.0199641 | downstream-variant-500B | FBXW4 | GRCh38.p7 | 10:101610321 | TTGGAAGTAGAACAC[A/G]GGATGTTAAGGCATT | 6468 |
rs569568670 | in-del | -/GTG | 0.00120676 | 0.0245341 | intron-variant | FBXW4 | GRCh38.p7 | 10:101615102 | TGCAATTTGTATAAC[-/GTG]GTGACCCCCCAAATT | 6468 |
rs569583068 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101646527 | AGGAGCAACAAAGCC[A/G]GGGCTTGTTGCTGGT | 6468 |
rs569623832 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101658952 | CACTGGAACGGATCA[A/G]TGCCATAAGTCAGAC | 6468 |
rs569640937 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101654643 | AACCCTGAAGAGATA[G/T]TTAAATAAACTGTCA | 6468 |
rs569649140 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101638206 | CTGGAAATAACCTAC[A/G]TGTCCATCAGTAGAA | 6468 |
rs569750948 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101680980 | AGAAATGACAAATGT[A/G]AGGATTGCAAAACAT | 6468 |
rs569806978 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101669244 | TAAACACCACAACTT[C/T]TCCTGAGTGCCATGA | 6468 |
rs569820021 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101656207 | GCTCAGCAGCTAGAA[A/C]GAAACCAGTCTGAAG | 6468 |
rs569866878 | snp | G/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101635864 | AAAAAAAAAGAGAGA[G/T]GGAGGGGCACCCCTC | 6468 |
rs569911620 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101662591 | GGGATTAAAACCCAA[A/G]TGTCATGGGAAGCCT | 6468 |
rs569932313 | snp | C/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101675352 | AGGACAAGAAACCAG[C/G]TTCATGCCAGGTGAA | 6468 |
rs569972887 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101663266 | AATCATTACAGCCAT[A/G]TGCCTATCATCTCCC | 6468 |
rs570013444 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101673126 | CTCTCCAGAAACAGC[C/G]CAAGTCTCCAGTGAC | 6468 |
rs570015104 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101683356 | ATTTTCCCAGCCCTC[C/T]TTCTCTTGCCTCAGG | 6468 |
rs570095754 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101667426 | GATCTGGGCCCCAAG[C/G]CTCTCCTGATGACTT | 6468 |
rs570157598 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101668183 | CTAGCTCTCCATCCT[A/G]ACTACCCTCTTTTAC | 6468 |
rs570170128 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101692248 | GTGACACACAATGAA[C/G]AGTTCAGATATAGAT | 6468 |
rs570193134 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101638957 | CACAGTAGGACTACA[A/G]AAGTAGGATCCATGA | 6468 |
rs570269795 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FBXW4 | GRCh38.p7 | 10:101633733 | AAGTGTTATTATATA[C/T]CAGCAATAACCAAGT | 6468 |
rs570330808 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101688124 | GGCTGACCCCAAATG[C/T]CTTTTCCATCTCTAA | 6468 |
rs570333449 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101634727 | ACCTCCCAGCAGATA[C/T]CAATCTCAGATGGAT | 6468 |
rs570407786 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101676780 | CCATACAGGAAAAGT[A/G]ATTCAAAACAGATCA | 6468 |
rs570459928 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101627950 | TTCTCTAACCCAGGT[A/G]ATTTAACCCAAACAA | 6468 |
rs570503663 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | FBXW4 | GRCh38.p7 | 10:101696705 | ATTTCAATGCGGCCA[A/G]AGAATTTAAGCCATG | 6468 |
rs570558261 | snp | A/G | 0.0023933 | 0.0345097 | utr-variant-3-prime, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101610838 | TGAACCCCCAGCCCC[A/G]AGAGGTTGGTCAAGG | 6468 |
rs570565390 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | FBXW4 | GRCh38.p7 | 10:101695769 | ATTCTTCATACCACC[C/T]ATTCGATTCACATGG | 6468 |
rs570672818 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FBXW4 | GRCh38.p7 | 10:101677332 | TATAATGGAATACTA[C/T]TCAGCAAAAAAAAGG | 6468 |
rs570683110 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101661267 | TCTGGGCCAGCCAGG[A/G]CTCGGAGAGTGCTGG | 6468 |
rs570707608 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | FBXW4 | GRCh38.p7 | 10:101626985 | TCTGGCCCACCCACA[A/T]CTGGCCCTGATCATC | 6468 |
rs570752874 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | FBXW4 | GRCh38.p7 | 10:101690250 | TCTACATTATCAAGT[A/G]ACAGCTGAATTCCAC | 6468 |
rs570771225 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101618031 | GGGCCAGGGCAGACA[A/G]AGCCACACCTGGGCA | 6468 |
rs570817653 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101689436 | TGTACTGTTTTATTT[C/T]GAACCTGTAAACTAA | 6468 |
rs570877598 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101637066 | TGTATATTTTGAAAA[C/T]TTCCGTTATAAAAAC | 6468 |
rs570883364 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101629324 | GAGTCTTGCTCTGTC[A/G]CCCAGGCTGGAGTGC | 6468 |
rs570902869 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101620824 | TCCATTCTGGTTTCA[A/G]TAAAGACCCAGTGTT | 6468 |
rs570937701 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101679845 | AGTCACCTGAATAGC[A/G]TACACTGTACCCAGT | 6468 |
rs571023365 | snp | A/C | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101655657 | TCTCTAGGACAGCTA[A/C]AGCTGCAGCTGCAAC | 6468 |
rs571051567 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101644396 | CAAACAGGGTCAGTA[A/G]GCCAAATAGCTTTCT | 6468 |
rs571069476 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101678697 | CCTCCCAAAGTGCTG[A/G]GATTACAGGCATGAG | 6468 |
rs571082228 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101664947 | AATAGTATTCATATT[C/T]AATATGACGAAACTG | 6468 |
rs571284655 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FBXW4 | GRCh38.p7 | 10:101631911 | GGATTATAGGCGTGA[A/G]CCACCGTGCCCAGCC | 6468 |
rs571328281 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101655348 | AAAGAAGGATTTTCC[A/G]GACCAAAGACTTCTA | 6468 |
rs571348020 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101632434 | CCTACAGAGAAACAC[A/G]AAATGATTATTCTCT | 6468 |
rs571364609 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | FBXW4 | GRCh38.p7 | 10:101625230 | TGGAAGGTGCTGCCC[A/G]TGGTCAGAAGTAGGA | 6468 |
rs571388047 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101647390 | TTCTTTGAAGTAGGA[C/G]AGTTTTACACATAGG | 6468 |
rs571401974 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101641729 | CCCAGATCAGAAAGA[C/T]ATTTGAAGTTGTAAA | 6468 |
rs571454355 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101693019 | GAAGACCCCAGTAAT[A/G]AATGGGCAAAGAGTG | 6468 |
rs571590265 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101658189 | ATGTACTGCCGCTTG[C/G]AAGTCCTGGGGACCA | 6468 |
rs571603263 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FBXW4 | GRCh38.p7 | 10:101675310 | AATTTTTGTGTTTAG[A/G]GCCATCTGGTAAACA | 6468 |
rs571649022 | snp | A/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101621624 | AGTTGAATGCCTCCA[A/T]GGTGACAGGCACTGT | 6468 |
rs571650134 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | FBXW4 | GRCh38.p7 | 10:101651095 | TCTGCACATTCCTTC[A/G]AGAAACAGGAGCACA | 6468 |
rs571652395 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101650567 | AACCGCCCCCCTCAA[A/G]GGGTGGTGGGGTGCC | 6468 |
rs571681629 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101643637 | CTGTGCCCACAGGGG[A/T]CTCTTTACCTAAACT | 6468 |
rs571736357 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101616417 | GTCCCTGCCTTCAAG[A/G]AGTATTCAATCCAGG | 6468 |
rs571741357 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101636148 | TGAGGTCAGGAGTTC[A/G]AGACCAGCCTGGCCA | 6468 |
rs571743744 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101644764 | ATCCAGCAGAACCCA[A/G]GACTGATGAAAAGGT | 6468 |
rs571804742 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | FBXW4 | GRCh38.p7 | 10:101636782 | TTAGTAGAGACGGGG[G/T]TTCACCATGTTGGTC | 6468 |
rs571818051 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101616853 | TAGTCCAGGCCCCGA[C/T]TGTAGATAAGGAAAC | 6468 |
rs571853446 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101674256 | ATCGCTTGAACCTGG[C/G]AGGCGGAGGTTGCAG | 6468 |
rs571854504 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101657325 | AGACAAGAAATAAAA[C/T]GCCTACTTCCAAAAG | 6468 |
rs571865240 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FBXW4 | GRCh38.p7 | 10:101619584 | GGATGGCGTGAACCC[A/G]GGAGGCGGAGTTTGC | 6468 |
rs571914469 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101666130 | GAGGAGACAAAGCTC[A/T]ATGGCTCCATTTTCC | 6468 |
rs571956315 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101620173 | CCAGCACCGCTCACC[A/G]CCCAACCCCAAGTCC | 6468 |
rs572021169 | in-del | -/AT | 0.00159617 | 0.0282053 | intron-variant | FBXW4 | GRCh38.p7 | 10:101692316 | TGTATATTATATATA[-/AT]ATATATATATAAACT | 6468 |
rs572112486 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101689589 | CCTGGGTAAGGCAGA[A/T]AACTGGAGAAAGCCT | 6468 |
rs572190754 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101659782 | CATGCAGAGCTAGTA[C/T]GTATGGTATGCATAC | 6468 |
rs572195082 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101660653 | AAAGGTGGAAAAACA[C/T]AGGCACGTTGCACAC | 6468 |
rs572255952 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101668397 | GGGAGAGGGAAGAAG[A/G]TCAAGGCATAGTATA | 6468 |
rs572262712 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101652365 | AAATCAGTCTCTCTT[C/G]CTTCGCCCTGGATAC | 6468 |
rs572333565 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101662734 | CGAGGAGCTGTGGGC[A/G]CCTCTCCCTTCCCCT | 6468 |
rs572361476 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101669840 | GCTCACTGCAAGCTC[C/T]GCCTCCTGGGTTCAT | 6468 |
rs572389460 | in-del | -/TGAC | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101613375 | GGAGTTTCCACAGAA[-/TGAC]TGGGGGAAATGAAGG | 6468 |
rs572401799 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | FBXW4 | GRCh38.p7 | 10:101637582 | GTGTGGTGGTGCATG[C/T]CTGTAATCCCATCTA | 6468 |
rs572426669 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101670688 | CCTCACACACAGTAG[A/G]CACTCATAAGAAAGA | 6468 |
rs572439481 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101672346 | AGCCAGTGTCATGCT[A/G]TTTATCAGCCTTACT | 6468 |
rs572443780 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101680180 | GATTTAGATTGCCAT[C/T]TCATACCACAATATA | 6468 |
rs572505641 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101629504 | GGCCAGGCTGGTCTC[A/G]AACTCCTGACCTCAA | 6468 |
rs572506131 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101690514 | TAGTGTTCACTGTTC[A/G]GGCAAGAGGCCTAAA | 6468 |
rs572513943 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101654780 | GGGAACATAGTATAA[A/G]ATATTTTATCAGAAC | 6468 |
rs572543377 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101684704 | AAGTATTTAAGCAGC[C/T]AAAGATAAGAACCTT | 6468 |
rs572682169 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FBXW4 | GRCh38.p7 | 10:101621193 | AGCAGGTTCACCTCC[A/G]CCTCCACTAGTCACT | 6468 |
rs572758550 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101611536 | TCTTCCAACCCTTTC[G/T]AGGCACGTCCTTGGC | 6468 |
rs572762750 | snp | A/G | 0.000288216 | 0.012001 | intron-variant | FBXW4 | GRCh38.p7 | 10:101673676 | CCAGGGCATCTGACT[A/G]AAATGATGGAAAAGA | 6468 |
rs572784443 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101666372 | CCTGCTATATCAGCC[A/G]TCAAATTGAAGAATT | 6468 |
rs572800829 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101666723 | GGTTCCAGAGAGCCT[C/T]GAAAGCAGAAGTCGG | 6468 |
rs572819854 | snp | A/C/G | 0.000133017 | 0.00815429 | missense, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101612403 | GACAGCAGTGTGAAA[A/C/G]GGGACTCATACATGA | 6468 |
rs572843163 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101657404 | TTGGGAGGCCAAGGT[G/T]GATGGCATCACCTGA | 6468 |
rs572854136 | snp | G/T | 0.000122377 | 0.00782134 | intron-variant, synonymous-codon, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101694425 | GTTGAGCGAGGCCCG[G/T]GCTATCCGGCGCCAG | 6468 |
rs572863916 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101658373 | AACATGGTGAAACCC[C/T]GTCTCTACTAAAAAT | 6468 |
rs572869817 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101682076 | TGTTATAAATCACTA[C/T]AAAAAAAGTTAATTA | 6468 |
rs572950554 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101646606 | GGGAAGGCCAGGGGA[C/T]GCAGAGCTGGGAGGG | 6468 |
rs572983904 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FBXW4 | GRCh38.p7 | 10:101632590 | AGCACAGAATTAATA[A/G]AGAGGGGAAAAAATA | 6468 |
rs573140400 | snp | A/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101614165 | CACAGTTCTCCTCCC[A/T]CTTCCAGATTTGGGG | 6468 |
rs573148473 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101626614 | CCTGCCTCAGCCTCC[C/T]GAGTTGCTGGGACTA | 6468 |
rs573158359 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101686390 | TCCCCACTCATTTGA[C/T]TACAGAATTAGTTTT | 6468 |
rs573186503 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101627254 | TTCTTTCCAAAAGCT[G/T]CCCTTTTCTCTCACC | 6468 |
rs573392787 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101622308 | AGACCACATGTGGGG[C/T]CTAGGGCAAGGTGAA | 6468 |
rs573459700 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101687697 | ACTTCATACAAATAC[A/G]AATCCCCCTCCAGGT | 6468 |
rs573477517 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101633879 | ACTTTAGGAGGCTGA[A/G/T]GGGGGTGGATCACCC | 6468 |
rs573516828 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101677054 | TCCTCTTTGTATTTG[A/T]TCATATATTTTTAGA | 6468 |
rs573525498 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101630338 | AGTGGGCTCCCGAAC[C/T]GCCCTGCTTGTGAAA | 6468 |
rs573610948 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101631058 | GGAAGATAAACACAA[A/C]TTTTTTTTTTTATCA | 6468 |
rs573633977 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | FBXW4 | GRCh38.p7 | 10:101630589 | CAAAGCATGAATACA[A/G]TGCGAAGGTCACAAA | 6468 |
rs573641976 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | FBXW4 | GRCh38.p7 | 10:101690819 | GACAGGTGAGAGAAA[C/T]GAAGCACAGTGCGTG | 6468 |
rs573736889 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101648582 | AGTCGATAATCTTTC[A/G]TGGACAGAACCAGCG | 6468 |
rs573804460 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FBXW4 | GRCh38.p7 | 10:101672171 | AGACACTATTGGGCC[C/T]CCTGCACCACCAACT | 6468 |
rs573835491 | snp | A/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101683680 | GTAGGTATATCGAAG[A/T]GGTCTTAAACAACAT | 6468 |
rs573848744 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101623251 | AACCCATCTCCAAAA[A/G]ACACACAAAAAATTA | 6468 |
rs573858151 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101637479 | TTGGGAGACCAAGGC[A/G]GGCAGATCACTTGAG | 6468 |
rs573880943 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101691645 | ATTTGAAAATAAACA[C/T]CAATTCTTTCATTCA | 6468 |
rs573910931 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101614068 | ATTCAGCCACCCTGG[A/G]CAGGCCAGAGCCCTG | 6468 |
rs573920122 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101645814 | GAGCTCAGCACAGGA[C/T]AGGCAAGCAGACAGA | 6468 |
rs573938625 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101643215 | ATTGTAATGATTAGC[A/G]TATCTACCCTTCAAT | 6468 |
rs574071576 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101651541 | TGAAACCAGGAGGCA[A/G]CAGCTTGGACAATTC | 6468 |
rs574099968 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101646526 | CAGGAGCAACAAAGC[C/T]GGGGCTTGTTGCTGG | 6468 |
rs574133550 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101652245 | AAAGTTTTCAGACAG[C/T]CATAGCTGCCCAAGC | 6468 |
rs574138517 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101663956 | GGTAGAAGGGTATGC[A/G]AGAGGCAGAAGAAAA | 6468 |
rs574143108 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101693252 | TTTGCTATAATGCCA[C/T]CTTGAGACTTTATCC | 6468 |
rs574152107 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101655123 | GTGTGTGCCACCATG[C/T]CTGGCCTATTTATGT | 6468 |
rs574226776 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101664573 | CATTGAGGGCAGGAA[C/T]ACTACAGGGGGAAGA | 6468 |
rs574245090 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101627183 | GTGTGAACCACTGGC[A/G]CTCAGCCTCCTGTGA | 6468 |
rs574273678 | snp | A/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101625744 | ACCTGGGCTTGAAAC[A/T]TAAACAGCAAGCAAG | 6468 |
rs574305474 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101618353 | ATCAAGGAGAGCTTC[A/G]TGGTGGAGGTGCTGT | 6468 |
rs574314118 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101663827 | GGGCCATCTTAACCT[A/G]TCCTTCTATCAATCA | 6468 |
rs574370914 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101691911 | ATTCAAAATTTACAA[A/G]AGTAGAGTAATCTTC | 6468 |
rs574380438 | in-del | -/A | 0.00398564 | 0.0444627 | downstream-variant-500B | FBXW4 | GRCh38.p7 | 10:101610272 | AAAACAAAACAAAAC[-/A]AAAAAAACAAAAACA | 6468 |
rs574411631 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101642947 | CTGTAAACTACCAAA[C/T]TATAGACTACTGATG | 6468 |
rs574529382 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101689502 | TAAGGCCTTTCCAAA[C/T]GCCGAAGACAATAAA | 6468 |
rs574591013 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FBXW4 | GRCh38.p7 | 10:101688836 | CCCAATTTTCTCCTC[C/T]TTTTTTCAAACAGTT | 6468 |
rs574598475 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101667603 | CAGAAGGGACACTTC[C/T]GGCTAACAGCTGGAC | 6468 |
rs574754923 | snp | C/T | 5.03884e-05 | 0.00501913 | synonymous-codon, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101611396 | GCTGAGGGGAGTCGA[C/T]GTCAGCGGGAAGGCC | 6468 |
rs574807730 | snp | G/T | | | upstream-variant-2KB | FBXW4 | GRCh38.p7 | 10:101696127 | GCATTGGGCTAGGCA[G/T]TAAAACTTGGAGGAG | 6468 |
rs574827837 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101670247 | GCAGAGAAAGCATGC[A/G]TAGGCTTTGGCATCT | 6468 |
rs574866333 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101683721 | ATCAGAAAACTCCTG[C/G]AACACAGATCAATTT | 6468 |
rs574882721 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101684496 | GCTGGTCTTGAACTT[C/T]TGACCTCAAATGATC | 6468 |
rs574891388 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101662679 | TTGCTAAGCACCTTT[A/T]TTTTCTTGGAGGGCA | 6468 |
rs574928255 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101682921 | ACTCAGCTTTTTCAT[A/C]TCTTTTGTCTAACCA | 6468 |
rs574930110 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101693121 | CAAAATAACACAACT[C/T]TGGTACCTTAAATGA | 6468 |
rs574963392 | snp | A/G | 0.000175562 | 0.0093675 | synonymous-codon, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101612342 | GCACACTCACCGGAC[A/G]CTGGTGCGGAGGTCC | 6468 |
rs574992154 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101692489 | GGCCAGGCGCCATGG[C/T]TCATGCCTGTAATCC | 6468 |
rs575001715 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101653404 | AACTCTGCTCTTCAA[A/C]ACCCTCCAAAACTAG | 6468 |
rs575003021 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101636657 | TAATGGTGCAATCTC[A/G]GCTCTCTGCAACCTC | 6468 |
rs575022036 | snp | C/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101653742 | GCAATTGCACTATAA[C/G]CTCCTACACGGTAAA | 6468 |
rs575111113 | snp | A/C | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101649884 | CCCCAGCCCCAGGAC[A/C]ACATGGATGCCAGAG | 6468 |
rs575145539 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FBXW4 | GRCh38.p7 | 10:101631902 | AAAGTGCTGGGATTA[C/T]AGGCGTGAGCCACCG | 6468 |
rs575200275 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101619838 | GGTCTTGATGGAATG[A/G]GGGGCTGAGGGAACA | 6468 |
rs575203543 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101674299 | GCACCACTGCACTCC[A/C]GCCTGGGCGACAGAG | 6468 |
rs575253310 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101665508 | GAAAACATAAGGCCT[A/G]GGTCTTCACCAAAGA | 6468 |
rs575261114 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101666249 | ACAGCGACAGGTTTA[C/T]AGGTTAGCCGACACC | 6468 |
rs575322120 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101626503 | CACAGGCATCTCTTT[A/T]TTTTTTGAGAGGAAT | 6468 |
rs575360901 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101639319 | ACACCATCAACAGCT[C/T]ACAAAGGAGGAATCC | 6468 |
rs575405638 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | FBXW4 | GRCh38.p7 | 10:101660136 | TTGAAGAGCTGAGAA[A/G]GCACAGGTCAGATAA | 6468 |
rs575536736 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101631788 | GCATGCCACCACGCC[C/T]GGCTAATTTTTTGTA | 6468 |
rs575575935 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101633747 | ACCAGCAATAACCAA[C/G]TGTTATTATATATCA | 6468 |
rs575599990 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101631920 | GCGTGAGCCACCGTG[C/T]CCAGCCATTATTTAC | 6468 |
rs575629547 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101650981 | TATGCCGGCAAATCT[C/T]CCGCCTGGGCCCTGA | 6468 |
rs575669609 | snp | G/T | 0.00216216 | 0.0328086 | intron-variant, missense, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101694603 | GACTCCCGAGCCGCC[G/T]CCTCCTCCTCCTCCT | 6468 |
rs575878735 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101687462 | AAAATACTTGCTTCC[A/G]GCCCATCTGTTCTCC | 6468 |
rs575894623 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101641096 | TCGGCCTCCCAAAGT[A/G]CTGGGATTACAGGCA | 6468 |
rs575934939 | in-del | -/AAGG | 0.00119737 | 0.0244387 | intron-variant | FBXW4 | GRCh38.p7 | 10:101660071 | CTGCCCCATGGCCCA[-/AAGG]AAGGAAGGAAGGGCG | 6468 |
rs575944967 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101686231 | TATTTAGCAGTGAAA[A/C]AAAGAATTTTATGGT | 6468 |
rs575951357 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101649708 | AGACAGTCTGAAGGA[C/T]GCCAACAGCAGCACA | 6468 |
rs575963006 | snp | G/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101658412 | TAGCCAGGCGTGGTG[G/T]CATGCGCCTGTAATC | 6468 |
rs575963617 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FBXW4 | GRCh38.p7 | 10:101645621 | TTCCTTCAATAAGTA[C/T]CCAGGGGTTCCCCAA | 6468 |
rs575964431 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101627711 | AAGGGTGCTTCACAT[C/T]TCACAATGAGCCCAC | 6468 |
rs576005773 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | FBXW4 | GRCh38.p7 | 10:101695158 | CGAGCCGCCACCGCC[G/T]CCGCCCCGGGAGGAG | 6468 |
rs576010185 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101654847 | TTACTTTTTTGAGAC[A/G]GACTCTTGCTCTGTC | 6468 |
rs576014015 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101650832 | TTAAAATCAACACTC[C/T]GTGAACACACAAAAC | 6468 |
rs576023074 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101637323 | TGTGAACCTGGGAGG[C/T]GGAGCTTGCAGTGAG | 6468 |
rs576081450 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101671214 | AGGAGGGAAACCCAG[A/G]CAGCATCCGGAAAGC | 6468 |
rs576128436 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101680401 | CAGGAAGGGAAAAAA[G/T]ATTAAAAGCAACAGA | 6468 |
rs576165705 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101652479 | AAATCCCACTGCCTG[G/T]TTTTGTGAGCTGAGG | 6468 |
rs576191437 | in-del | -/AC | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101632211 | CCACACATATTCTCT[-/AC]ACACACACACACACA | 6468 |
rs576246032 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101637220 | AACCCCATCTCTACT[A/G]AAAATACAAAAAAAA | 6468 |
rs576338417 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101690749 | GAGGCTCTTCGTCCC[A/G]GAGTGCAGGCCATAA | 6468 |
rs576343769 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101663694 | AAGTTGCTCAGAATT[C/T]CATGTGACCTCAGGA | 6468 |
rs576400788 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101646757 | GGGAGAGGGAGAAGG[A/C]TGAAAGGTTTGGGGG | 6468 |
rs576411775 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | FBXW4 | GRCh38.p7 | 10:101653907 | GCAGGTGGATCACGA[G/T]GTCAAGAGATCGAGA | 6468 |
rs576473590 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101659491 | AAAGCTACCTAGAGA[A/C/T]CAGCAGTGGGAAAAC | 6468 |
rs576489404 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101681384 | CAAGAGCGAAACTCC[A/G]TCTCAAAAAAAAAAA | 6468 |
rs576584891 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101612574 | GGGGAAATGTTCTCT[C/T]TCCTCAGCTAGAATG | 6468 |
rs576660466 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101613224 | AATTCCCTCCGTGAC[C/T]GCGGCAGTGGGCAGA | 6468 |
rs576747049 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101666834 | GGCCAAGATGGGAGG[A/G]TCACTTGAGGCCAGG | 6468 |
rs576762884 | snp | A/C | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101623519 | AAAGATACTCCAAAA[A/C]ATAGCTTGGCAGGTA | 6468 |
rs576772705 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101658031 | GCCAAATGGCACTAC[C/T]GTAATGATGAAACTC | 6468 |
rs576800697 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101655289 | CAATTTAAAAACTCT[A/G]ACTTTTCCTCTTTTT | 6468 |
rs576817791 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101650944 | TCCAAGTGACTAAGC[A/G]CAGGGTGGGAAATAA | 6468 |
rs576873647 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101651390 | GATACATTTCAAAGT[G/T]TCTCTAGCAATTTGG | 6468 |
rs576880577 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101642211 | ACATGTGTATGTGTT[C/T]AGGATATATGTCTAT | 6468 |
rs576920877 | snp | C/G | 0.00119737 | 0.0244387 | upstream-variant-2KB | FBXW4 | GRCh38.p7 | 10:101696117 | TTTTCTATTAGCATT[C/G]GGCTAGGCAGTAAAA | 6468 |
rs576929372 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | FBXW4 | GRCh38.p7 | 10:101625623 | GGTATAAAGGATCCA[C/T]GCAGTGGGCCAGGCT | 6468 |
rs576985671 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101626404 | TGGGCTGGAAACATA[A/G]TAGCCACTTGGAAAT | 6468 |
rs576990202 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101616518 | CAACGGAAAGTTCTA[C/T]AAGGGGGCAGCTAAG | 6468 |
rs577202820 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101687826 | CTAAATGCTCTTCAA[C/T]TCTGTCTAAAAACAC | 6468 |
rs577260845 | in-del | -/AC | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101624094 | TAGACACAGACAGAC[-/AC]ACACACACACACACA | 6468 |
rs577271692 | snp | C/T | 0 | 0 | intron-variant | FBXW4 | GRCh38.p7 | 10:101628275 | CTCAGTCCCATCTCT[C/T]CCCTCAGGGGTATTC | 6468 |
rs577286664 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101669622 | TTGGCCCAGCAGCAC[A/G]TCACCCTCCAGAAAC | 6468 |
rs577315355 | snp | A/G/T | 6.62969e-05 | 0.00575714 | missense, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101611371 | TGAGACGCAGGCAGT[A/G/T]CACAGGGCTGCTGAG | 6468 |
rs577367421 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101668593 | CTAGTGTCACCAAAA[A/G]TAGCAGAAAAGCTTA | 6468 |
rs577433105 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101660794 | AGGCAGTGGGAGGAA[C/G]AGAAAGATGACTGAT | 6468 |
rs577533911 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101681879 | AGAGCAGATTAAATA[A/C]AACTGAAAAAGCACA | 6468 |
rs577588400 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101623511 | AAAATGATAAAGATA[A/C]TCCAAAAAATAGCTT | 6468 |
rs577609277 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FBXW4 | GRCh38.p7 | 10:101627382 | GTAAAAAACCATCAA[C/T]AGTCAAGCAGATTTT | 6468 |
rs577611273 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101635929 | CCTGGGGGGGCGGGC[A/G]GAGGGAAGAGCGATC | 6468 |
rs577651505 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101614430 | TGGGCTGCCAAGCTG[G/T]GCCCCTACCCCAGCA | 6468 |
rs577668573 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101631691 | GGAGTGCAGTGGCGC[A/T]ATCTCGGCTCACTGC | 6468 |
rs577726167 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101692721 | ACTGCACTCCAGCCC[A/G]GGCAACAAGAGTGAA | 6468 |
rs577742184 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101646736 | TACCCAGCAAATAAA[C/G]CCACAGGGAGAGGGA | 6468 |
rs577831302 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101664637 | TGCAAAAGAGCAGGG[A/T]AACTTCCTGGGGCCA | 6468 |
rs577833175 | snp | A/G/T | 0.000132631 | 0.00814245 | intron-variant | FBXW4 | GRCh38.p7 | 10:101673441 | AGGCAGAATGTCCCC[A/G/T]AAGTATAAGATGGAA | 6468 |
rs577873699 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101682745 | CAAAGTTGAACTTTA[A/G]AAGCTGCTACCAAAC | 6468 |
rs577927702 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101649620 | CCTTTGGGATTTAGG[C/T]CCCTCAAAGACCTTG | 6468 |
rs577935610 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | FBXW4 | GRCh38.p7 | 10:101643131 | AGAAAGCATGTGTCC[A/G]CCCAGGCCACTGATT | 6468 |
rs577950504 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | FBXW4 | GRCh38.p7 | 10:101625456 | AGTGGGATGGGAGTC[C/T]GCCAGAGTCCTCTGA | 6468 |
rs577981852 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101640260 | AGTAGGGGGTGAGGA[A/G]ATGGTCTGGACAACA | 6468 |
rs577995051 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101639262 | GCAACCAGGTTCTTT[C/G]TCTGTGCATGTCACA | 6468 |
rs578018343 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | FBXW4 | GRCh38.p7 | 10:101646800 | GTTCTGGGGTATTTA[A/G]TTGGTTTGAAAAAAT | 6468 |
rs578098920 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FBXW4 | GRCh38.p7 | 10:101655756 | GTCTCGTGCTCTGGA[C/T]TGGACCCTCTCCAGC | 6468 |
rs578142536 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FBXW4 | GRCh38.p7 | 10:101613487 | AGAAACAAGGCCGTG[A/G]ACACTTCACAGGGAT | 6468 |
rs578156188 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101656685 | GGATTATGGCTTTGC[C/T]GTGGGAAGGAGCGGA | 6468 |
rs578205602 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101665294 | GACTCCAAGACCTCA[A/G]TTCTGGAGTTAGGGG | 6468 |
rs578233191 | snp | A/G | 0.000848986 | 0.0205857 | intron-variant, synonymous-codon, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101694455 | GAGCAGATCGCAGCT[A/G]GTGAAGCGCCGCAGC | 6468 |
rs578248715 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101693484 | TAGGATCAGTAAGAT[A/G]GCAATTATATGTGCA | 6468 |
rs745429228 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101613324 | AACATCAAGTGCACC[C/T]GCTAATCCCTGCAGC | 6468 |
rs745489846 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101635918 | TTCCTCCCTACCCTG[A/G]GGGGGCGGGCGGAGG | 6468 |
rs745500210 | snp | G/T | 1.65633e-05 | 0.00287774 | missense, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101611743 | AGGGTGCTGTCGTGG[G/T]GCTCCTCCCACTCCA | 6468 |
rs745510225 | snp | C/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101650896 | AAAGATCGGGCTCTC[C/G]AGAGACGCGGCCTGT | 6468 |
rs745513230 | snp | A/C | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101653028 | TTCCAGGCAACCATT[A/C]CTGGGCTGTCTCTGG | 6468 |
rs745521092 | snp | A/G | 4.9769e-05 | 0.00498819 | intron-variant | FBXW4 | GRCh38.p7 | 10:101676441 | CACTGGTCATCCTAT[A/G]TCCAGACAGAACAGA | 6468 |
rs745534799 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101613959 | CCTGAGAGGGATCAG[A/G]CAGAAGGCCTTCTCC | 6468 |
rs745582373 | snp | C/T | 1.77558e-05 | 0.00297953 | missense, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101612337 | GCCCAGCACACTCAC[C/T]GGACGCTGGTGCGGA | 6468 |
rs745600384 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101668985 | CAGGCAGGACCTTAG[A/G]TGGAAGAACTTTAAA | 6468 |
rs745633412 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101673884 | GTGATCTAAACTTCC[C/T]TGGACTTTGTAAAAG | 6468 |
rs745806337 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101674992 | CAAGAACAGCCACCA[C/T]CTCCTATTCCCAAGC | 6468 |
rs745827540 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101659186 | ATCTGAGCCCAAGCA[A/G]CACCTGCAGAGGGGT | 6468 |
rs745856020 | in-del | -/AAT | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101652542 | CCTCAAGAAGAAAAA[-/AAT]AATAATAACGACAGG | 6468 |
rs745872245 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101682340 | TTAAATCACTATAGA[A/G]CCACCTACACTACCA | 6468 |
rs745883767 | in-del | -/GGCA | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101618634 | TTGCCACACACACAG[-/GGCA]GGCAGCACAGGACCT | 6468 |
rs745989702 | snp | A/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101645858 | GAAAAAGCATGACCT[A/T]TGGAGTCAGATGCCA | 6468 |
rs746013245 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101636617 | TTAAAGATGGAGTCT[C/T]GCTCTTGTTGCCCAG | 6468 |
rs746056518 | snp | C/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101668635 | CTTCCATATCTCCTA[C/G]AGGTTAAAAATATTG | 6468 |
rs746069662 | in-del | -/AG | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101692101 | ATTTTTTTTTTTGAC[-/AG]AGAGTTGAACAGAAG | 6468 |
rs746084961 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101651633 | CCTCTATAAGGGCTC[C/T]CATCGGGGGTTGCTT | 6468 |
rs746085418 | snp | C/T | 5.68489e-05 | 0.00533115 | intron-variant, missense, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101694622 | CCTCCTCCTCCTCCT[C/T]CCCGGCCGCCGCCGC | 6468 |
rs746120994 | snp | C/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101631770 | GTAGCTGGGAATATA[C/G]GCGCATGCCACCACG | 6468 |
rs746121050 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101646700 | AGTAACCCAAAGGAG[A/G]CTGGAGAGAGCACTT | 6468 |
rs746179406 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101654740 | TCTGTGTCATCCTTT[C/T]AATGGCTACATAGCA | 6468 |
rs746189867 | snp | C/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101619900 | GAGAAGCAGCATTGG[C/G]TGTCTGAGGGTGAGT | 6468 |
rs746230056 | in-del | -/AAG | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101678955 | TATTTTTGGTTAATA[-/AAG]TAGTAAATGCACAGG | 6468 |
rs746243183 | snp | G/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101615412 | GTCAAGTCCAGCAAT[G/T]CTCTCTCCACCCAGG | 6468 |
rs746280362 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101617697 | GAAGGGGCAGCCGCG[C/T]AGATAAAAGGATACA | 6468 |
rs746357841 | snp | A/C | 0.000281692 | 0.0118645 | intron-variant | FBXW4 | GRCh38.p7 | 10:101673443 | GCAGAATGTCCCCGA[A/C]GTATAAGATGGAAAA | 6468 |
rs746360264 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101677296 | AACAGGAAAGTGGAT[A/G]AACACACTAGGGTAG | 6468 |
rs746377979 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101655826 | ATGTGCTAAGCAGTG[A/G]CTGATTACATCTGGA | 6468 |
rs746440331 | snp | A/C | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101691406 | AAACCCGAGCAGTGA[A/C]CCTGCTCTTTATCAA | 6468 |
rs746466632 | snp | G/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101681571 | AAATACAAAAAATTA[G/T]CCAGGCGTGGTGGCG | 6468 |
rs746474750 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101678532 | TCGGGTTCACATCAC[C/T]CTCCTGCCTCAGTCT | 6468 |
rs746538131 | snp | C/T | 1.65482e-05 | 0.00287643 | missense, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101611738 | AGTACAGGGTGCTGT[C/T]GTGGGGCTCCTCCCA | 6468 |
rs746567423 | snp | A/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101626517 | TTTTTTTTGAGAGGA[A/T]TCTCCCTCTGTCACC | 6468 |
rs746640817 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101644358 | CTATTACCTACATTG[C/T]CATCCTCCCAATCTG | 6468 |
rs746642677 | snp | C/T | 3.29457e-05 | 0.00405854 | missense, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101673585 | GACGATTCAAGCTGG[C/T]ACCATCTGGACGGAA | 6468 |
rs746693690 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101611594 | ATAATCATGAGTCCT[A/G]GCATGCTGGAGAAGA | 6468 |
rs746698346 | in-del | -/C | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101653957 | CAAACCCCATCTCTA[-/C]TAAAAATGCAAAAAT | 6468 |
rs746747365 | snp | A/C | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101686327 | AGTGCCTTTAATCCC[A/C]AATGGACATTGTGAT | 6468 |
rs746884691 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101621279 | CACCTATAATCCCAC[A/G]ACTTTGGGAGGCCAA | 6468 |
rs746885390 | snp | A/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101673446 | GAATGTCCCCGAAGT[A/T]TAAGATGGAAAAGGG | 6468 |
rs746958482 | snp | C/T | 1.64768e-05 | 0.00287021 | missense, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101624782 | GGGGTGAGAAGTGCC[C/T]GCAACAAGCCGTCCC | 6468 |
rs746978430 | snp | C/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101635594 | AATCTCAGCATTTTG[C/G]GAGGCCAAGGCAGGC | 6468 |
rs747029554 | snp | C/T | | | upstream-variant-2KB | FBXW4 | GRCh38.p7 | 10:101695531 | AGGGCCCAACGAATC[C/T]GCAGCCCTAGAAGTT | 6468 |
rs747039293 | snp | A/G | 0.000108231 | 0.00735553 | intron-variant, missense, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101694441 | GCTATCCGGCGCCAG[A/G]GCAGATCGCAGCTGG | 6468 |
rs747092369 | snp | C/G | 2.69764e-05 | 0.00367253 | intron-variant, missense, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101694597 | GCAGCCGACTCCCGA[C/G]CCGCCTCCTCCTCCT | 6468 |
rs747143620 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101631084 | TATCAAACTAAAGCC[A/G]AATAAGAACAAGATG | 6468 |
rs747156094 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101622918 | AGAAGACTGGCATGG[C/T]TCTTATGCAAGAATG | 6468 |
rs747166203 | snp | G/T | 1.737e-05 | 0.00294698 | intron-variant | FBXW4 | GRCh38.p7 | 10:101611429 | GAAGGGAGGGCACAG[G/T]AAGTGGTAAGAGCTT | 6468 |
rs747231796 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101685866 | TTCCAAAAACATGGT[C/T]CTCCCTTTGGCAAGT | 6468 |
rs747237251 | snp | C/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101644495 | AATAGGAAAAAGATG[C/G]CAAACTGAACCTGAG | 6468 |
rs747242246 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101630139 | TTTGTACAAATGAAG[A/G]CCAGGCTGCCTAATA | 6468 |
rs747329891 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101683353 | GCCATTTTCCCAGCC[C/T]TCCTTCTCTTGCCTC | 6468 |
rs747349183 | in-del | -/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101648150 | TGGGTTTTTTTGTTT[-/G]TTTGTTTTTTCCTGT | 6468 |
rs747361074 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101651294 | CCTACACTCTGGAGC[A/G]CCCAGAGAGAAAACA | 6468 |
rs747395437 | snp | C/T | 1.6554e-05 | 0.00287693 | synonymous-codon, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101611363 | CTTGGTGGTGAGACG[C/T]AGGCAGTACACAGGG | 6468 |
rs747450969 | snp | A/C | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101614499 | CTGCAGTCAGAAATA[A/C]AGGACAGCCCAAGGG | 6468 |
rs747499790 | snp | A/G | 0.000198626 | 0.00996362 | intron-variant | FBXW4 | GRCh38.p7 | 10:101668031 | GCCTGGGATCAGTGG[A/G]GAGGAGAGGTGCTCC | 6468 |
rs747502682 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101615991 | ATGTCCGTGGCTCCC[A/G]CACCATTTTTCAGTC | 6468 |
rs747530899 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101668386 | TTGGAGAAGTAGGGA[A/G]AGGGAAGAAGATCAA | 6468 |
rs747541668 | snp | G/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101691359 | TTCTCTCCACCTGCT[G/T]TAACACGCATAACTT | 6468 |
rs747630215 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101675384 | AGTGGAGAATCCCAG[A/G]GCAGCCTGGTAACTG | 6468 |
rs747668405 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101619474 | CCATCCTGGCTAAGA[C/T]GGTGTAAACCCTGTC | 6468 |
rs747686570 | snp | C/T | 8.23608e-05 | 0.00641667 | missense, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101673569 | AAGACTCCCAGAGGC[C/T]GACGATTCAAGCTGG | 6468 |
rs747689411 | in-del | -/A | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101678004 | AAAGCAAATACAGCC[-/A]AATATTAATTGTAGA | 6468 |
rs747713986 | in-del | -/C | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101651197 | GTCCTTCCCCCCAGG[-/C]CCCAGCTCTGTGAGC | 6468 |
rs747719817 | snp | A/C/G | 3.55443e-05 | 0.00421558 | intron-variant | FBXW4 | GRCh38.p7 | 10:101611450 | GTAAGAGCTTTCCAA[A/C/G]TGGGACATGGGTGTG | 6468 |
rs747744001 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101626282 | GGAAGCAGCCAGTGG[A/G]TACTGAAGAACCAAA | 6468 |
rs747744363 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101639365 | TAATAATGTGAGGGG[A/G]AGGAGGTCAAAGGCT | 6468 |
rs747771519 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101662577 | GAAGCGGGAGAGAAG[A/G]GATTAAAACCCAAGT | 6468 |
rs747784365 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101641132 | CACCGCGCCCAGCCA[A/G]CCCTTCCATTTTCAA | 6468 |
rs747809520 | snp | A/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101677309 | ATAAACACACTAGGG[A/T]AGGTTCATATAATGG | 6468 |
rs747815064 | snp | C/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101677143 | TGGGAAAAGGTCTGG[C/G]AGTTTATTATAAATC | 6468 |
rs747833753 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101624908 | TCATTCCCTAGGGGA[C/T]TGTGGGTTAAGCCAG | 6468 |
rs747849137 | in-del | -/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101671453 | ATGAAATTAACCCAG[-/T]TATCTCAAACAAACT | 6468 |
rs747890003 | snp | C/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101647321 | CTGACCCTGTACCTT[C/G]CTTGGGTGACTACCA | 6468 |
rs747891974 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101664093 | CATGACTCTTTACAA[A/G]TCAAGAACTCAAAGT | 6468 |
rs747955894 | snp | A/T | 1.64743e-05 | 0.00287 | missense, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101624754 | TCTTACCTGTTGAGG[A/T]CCCAGATTCTCAGGG | 6468 |
rs748023579 | snp | A/C | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101633690 | TATACCAGCAATAAC[A/C]AAGTGTTATTATATA | 6468 |
rs748075263 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101686166 | TTGGTTAGGTTCTGT[A/G]TTTGCACGGCACTTG | 6468 |
rs748077674 | snp | C/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101670410 | ATAAGTATAAGGCAT[C/G]TAGCACAGCAGCAAA | 6468 |
rs748093980 | in-del | -/A | | | upstream-variant-2KB | FBXW4 | GRCh38.p7 | 10:101695938 | ATTTTGAAGCCATAC[-/A]AAAAAAAAGAATGCA | 6468 |
rs748115362 | in-del | -/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101687636 | CCTATCAAACTCCTA[-/T]TTCACTATAATTTCC | 6468 |
rs748122954 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101632942 | AGAAAATCCAAAAGA[C/T]TCAACCAAAAAACTA | 6468 |
rs748135879 | snp | A/G | 1.73688e-05 | 0.00294688 | intron-variant | FBXW4 | GRCh38.p7 | 10:101612480 | CATCAGCTGCCCACT[A/G]GGAAGGGAAGGACGG | 6468 |
rs748146938 | snp | C/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101692949 | GGATCAAAGATGACA[C/G]ACTAGATTCTAACAT | 6468 |
rs748161418 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101685210 | TGACTCTTCCAAACA[C/T]GCCATCTGAACTGTT | 6468 |
rs748178921 | snp | C/T | 6.66778e-05 | 0.0057736 | intron-variant | FBXW4 | GRCh38.p7 | 10:101676478 | AATCACTACAACTTA[C/T]TGCCAACCACAGAAA | 6468 |
rs748221128 | snp | C/T | | | intron-variant, downstream-variant-500B | FBXW4 | GRCh38.p7 | 10:101625498 | AACAACGCCGAGAGG[C/T]ACACGAGAAGGAGCA | 6468 |
rs748297658 | snp | A/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101630241 | TCTGAGCCTTATTAC[A/T]CTCTATTACTCCAAT | 6468 |
rs748310097 | snp | A/G | 3.29538e-05 | 0.00405904 | synonymous-codon, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101672960 | AATGATGCCCCCTTT[A/G]CAATCCACACAGTTC | 6468 |
rs748318237 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101658797 | CCCAGCCCCTAGTCT[A/G]CTTACAAGAGTAAGC | 6468 |
rs748393838 | snp | C/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101680041 | GGCCTCCAATTCCAT[C/G]CAAGTTGCACAAAAG | 6468 |
rs748394831 | snp | A/G | 1.7119e-05 | 0.00292562 | utr-variant-3-prime, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101611248 | AAGAGAAGTCCCTGA[A/G]TAGCTGGTTTCCCTG | 6468 |
rs748419417 | snp | A/C | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101657741 | AGCAGATGTCCAATC[A/C]GTAGTCAGAGACCTT | 6468 |
rs748433815 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101620907 | GTGCCTTAGAACTCC[A/G]TCCTGACCATAAATC | 6468 |
rs748510511 | snp | G/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101644311 | GGGCAGCTGGGACTG[G/T]GGCCTGGGCAAGGGA | 6468 |
rs748556071 | snp | C/T | 1.65222e-05 | 0.00287417 | intron-variant | FBXW4 | GRCh38.p7 | 10:101668017 | CTCTCGTTGGCATTG[C/T]CTGGGATCAGTGGGG | 6468 |
rs748587409 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101614474 | TGGAAAATGTCATGG[C/T]CGTAAGTATCTGCAG | 6468 |
rs748635608 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101651141 | CCAGCTCTGTCCCCC[A/G]GGGATTGTACAGGCC | 6468 |
rs748660299 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101666765 | CACTTGTCCATAGGT[A/G]AAGTTAGAGATATAA | 6468 |
rs748661579 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101665812 | GCCTAACACATTCCA[A/G]AGGAGGAGGCTGGAA | 6468 |
rs748715809 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101672841 | TCTCAGCCAATCCTG[A/G]GACTCAGGGATCTAT | 6468 |
rs748746239 | snp | A/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101682074 | CATGTTATAAATCAC[A/T]ACAAAAAAAGTTAAT | 6468 |
rs748810766 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101650875 | GGGGGAGCACACATC[A/G]GATACAAAGATCGGG | 6468 |
rs748844314 | snp | A/G | 1.64825e-05 | 0.00287071 | synonymous-codon, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101672996 | CTGTTCATGAGCCGA[A/G]TACTTGACAGTGAAG | 6468 |
rs748855047 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101615795 | CCGCCAGGGACAGGC[C/T]CTGAGTGCTAAGCTG | 6468 |
rs748875807 | snp | C/G | 1.67008e-05 | 0.00288965 | missense, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101612425 | CATACATGACATCCA[C/G]CACCCCAGCCCCTGG | 6468 |
rs748882229 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101623374 | GCAATATAATGAGAA[C/T]CTGTATCTCTAAAAA | 6468 |
rs748932721 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101669549 | TTGGTCTCCAGGAGC[A/G]GCTGAGGAAGCATGC | 6468 |
rs748936006 | snp | A/C | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101639330 | AGCTTACAAAGGAGG[A/C]ATCCTTATTTGCTGA | 6468 |
rs749032202 | in-del | -/C | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101649868 | GATTCCAGATGATGG[-/C]CCCCAGCCCCAGGAC | 6468 |
rs749043483 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101660812 | AAAGATGACTGATCC[A/G]TCCAGCGTGCTCCCA | 6468 |
rs749117558 | in-del | -/AAACA | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101634230 | GAAAAATGAACAAAT[-/AAACA]AAAATCACTAGAAAA | 6468 |
rs749161084 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101683921 | CAAGGAGGGGAAAAC[A/G]GGGTTACACAAAATG | 6468 |
rs749218179 | snp | C/G | 1.6636e-05 | 0.00288405 | intron-variant | FBXW4 | GRCh38.p7 | 10:101676313 | TTTATGTCCCAAGTA[C/G]CTTTTAAAAAGTCAA | 6468 |
rs749264085 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101646108 | GCCATAGAGCATCAA[C/T]TGGGATTCTTGATCA | 6468 |
rs749271242 | snp | A/C | 9.97589e-05 | 0.00706183 | intron-variant | FBXW4 | GRCh38.p7 | 10:101676463 | CAGAACAGATAATCC[A/C]ATCACTACAACTTAT | 6468 |
rs749276911 | snp | A/T | | | upstream-variant-2KB | FBXW4 | GRCh38.p7 | 10:101695302 | GACACCACCCCCGCA[A/T]CCCCGAGAGCGCTTG | 6468 |
rs749379807 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101632788 | GGCAAGGTGTCCCTG[C/T]ACTAAAGCAAAAACT | 6468 |
rs749437242 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101659901 | CTTCTCCAAGAGTCA[A/G]TGGGGTAGGTGGAAG | 6468 |
rs749452231 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101619159 | ATCACAGGGCCTAGC[C/T]AGGGATACTTCAGTG | 6468 |
rs749537088 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101670092 | CTTTTAAAAAGCAGA[C/T]TGGTGATACGCATCA | 6468 |
rs749540043 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101617903 | AAAGAAAAAAGAGAA[C/T]GAAAAAAAGCTATCA | 6468 |
rs749549777 | snp | A/C | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101693229 | CAGCACCTCTGCAAA[A/C]CATAACCTTTGCTAT | 6468 |
rs749559265 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101633398 | TGGGAGCTGAACAAT[A/G]AGAACACATGGACAC | 6468 |
rs749692949 | snp | C/T | 8.24341e-05 | 0.00641952 | missense, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101611650 | CAGGCCCTTTGACGC[C/T]GGTCCCACAGCCGTA | 6468 |
rs749706270 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101624038 | GTGGTGATGGTTATC[C/T]GAATCTACACGTGAT | 6468 |
rs749731095 | snp | C/T | 0.000416844 | 0.0144308 | intron-variant | FBXW4 | GRCh38.p7 | 10:101676294 | TTTTACTTTCCATTA[C/T]GCTTTTATGTCCCAA | 6468 |
rs749785786 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101628063 | GCTCCTGTGCTAGGC[A/G]TGTCAAAGGCTCTCA | 6468 |
rs749786757 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101626696 | GGTTTCACCATGCTC[A/G]CCAGTCTGGTCTCGA | 6468 |
rs749802232 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101642742 | TAATTTCACCTCTTT[A/G]GAACATTGGAATAAA | 6468 |
rs749803824 | in-del | -/A | 1.65206e-05 | 0.00287403 | frameshift-variant, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101611344 | CAGGGCAGCATAGAG[-/A]ATGCTTGGTGGTGAG | 6468 |
rs749808655 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101682214 | GAAATTGTTCCTCCA[A/G]TATCAAACATTTGTT | 6468 |
rs749842767 | in-del | -/TGTT | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101614257 | ATAGAAGTAATTTCA[-/TGTT]TGTTTGAAATAGAAG | 6468 |
rs749866092 | snp | A/C | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101678795 | TTACTAAAAGCCAGC[A/C]AGCAAGTCCAGCTTT | 6468 |
rs749932996 | snp | A/G | 1.66324e-05 | 0.00288374 | synonymous-codon, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101612405 | CAGCAGTGTGAAAGG[A/G]GACTCATACATGACA | 6468 |
rs749970497 | snp | A/G | 1.88532e-05 | 0.00307022 | intron-variant, missense, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101694517 | CCCGCATGTCCAGGT[A/G]GGAGCAGATGAGCAG | 6468 |
rs750012338 | snp | G/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101632008 | GGCAGACCTGAAGGT[G/T]AGCGACCTGGTACAG | 6468 |
rs750032196 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101615425 | ATTCTCTCTCCACCC[A/G]GGGAAACATAAAGAC | 6468 |
rs750083482 | snp | C/G | 0.000165851 | 0.00910484 | intron-variant, missense, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101694410 | CCGCGTGAAGCCGGA[C/G]TTGAGCGAGGCCCGG | 6468 |
rs750103459 | snp | A/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101682568 | AAGGGAGTACTCTGG[A/T]TCATAGCAGGAAGAA | 6468 |
rs750179110 | in-del | -/A | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101675952 | TAGAGTAGAAGATTT[-/A]AATAAAAATATTTGT | 6468 |
rs750179123 | snp | A/C | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101617317 | TGCAGCCACTCCATC[A/C]CTGGCCCCTCAACAT | 6468 |
rs750201843 | snp | C/T | 3.30803e-05 | 0.00406682 | missense, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101611314 | TTTGAAAATCCAGGA[C/T]GTGGAGGTTGTAAGA | 6468 |
rs750273757 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101624451 | TCTCTGGGGATAGAT[A/G]GGATTTTATATAGCC | 6468 |
rs750319766 | snp | A/G | 8.24722e-05 | 0.006421 | intron-variant | FBXW4 | GRCh38.p7 | 10:101667998 | AGAAACAGGAGAGGA[A/G]ATGCTCTCGTTGGCA | 6468 |
rs750342773 | snp | C/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101672503 | CATTTTAATTATCAG[C/G]CTGATTGCTTATAAA | 6468 |
rs750361559 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101639121 | TCATGCAGCTTGCTA[A/G]TCATTTTCCTTTGGA | 6468 |
rs750444653 | snp | C/T | 1.64912e-05 | 0.00287147 | synonymous-codon, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101672921 | CCACCTCACCTTGGC[C/T]GTCCTGTCCCTGGAG | 6468 |
rs750454044 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101677910 | TAAACTAATATACTC[C/T]AGTCAATGATATGTA | 6468 |
rs750467921 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101611106 | TTCCTGGGAGGGACT[A/G]CATCTCTGGTAAGCT | 6468 |
rs750557282 | snp | A/G | 1.64874e-05 | 0.00287113 | synonymous-codon, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101611700 | ACCTGTGGCCAGCAG[A/G]TGGTTGCCATCTGTC | 6468 |
rs750564258 | snp | A/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101662038 | GTACTCAGCGAGTTA[A/T]GAAGTCCAGGGCCAA | 6468 |
rs750585091 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101625698 | TCTTGTTAGAGGATT[C/T]GGTAGGGTGGAGAGG | 6468 |
rs750616504 | snp | A/C | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101663749 | CTGAAGGTATTCCTG[A/C]CCCATAATTATACTC | 6468 |
rs750682859 | in-del | -/TAATAAT | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101681401 | CTCAAAAAAAAAAAA[-/TAATAAT]AATAATAATAATAAT | 6468 |
rs750729340 | snp | C/T | 1.7849e-05 | 0.00298734 | intron-variant | FBXW4 | GRCh38.p7 | 10:101611809 | GGGAGGTTTAGGGTA[C/T]CCTCCACCTCTACCC | 6468 |
rs750752100 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101685840 | TGCTTAGGAACTGCT[C/T]AAGCAAGAGTTTCCA | 6468 |
rs750783891 | in-del | -/AAA | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101637702 | AAGATCCTGTCTCAA[-/AAA]AAAAAAAAAAAAAAA | 6468 |
rs750843834 | snp | C/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101649286 | TTGCCCTCCCAGCCA[C/G]GCCTTGGCAGGGCAG | 6468 |
rs750902994 | in-del | -/TGTT | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101638907 | GCTTCATAACCACTC[-/TGTT]TGTAAAGAGATGCTA | 6468 |
rs750916921 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101672404 | GGACCGGGCAATTTG[A/G]CAAAGATGCAACAAA | 6468 |
rs750933234 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101670989 | GTACATATTTGGGAA[A/G]CTCCCCAAAAATAGA | 6468 |
rs750966814 | snp | A/C | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101619082 | ACAAGATGAGCCTTG[A/C]TTCCTCCAAACTCCA | 6468 |
rs750991422 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101634756 | ATTAAGGAGATAAAC[A/G]TTTTTAAACTGTATG | 6468 |
rs751067976 | snp | C/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101642518 | CCTGCTCCTCTCCAA[C/G]CTACAACACCCCTCT | 6468 |
rs751078437 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101694227 | AAAGGGGTCCCCGAG[A/G]GTGCTCGGGAAAGGG | 6468 |
rs751132324 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101628929 | TCAACCTGCCTTACT[C/T]GTCCCCTGGCCCTAG | 6468 |
rs751153139 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101629403 | ATTCTCCTGCCTCAG[C/T]ACCCCCAGTAGCTGA | 6468 |
rs751239309 | snp | C/T | 3.32674e-05 | 0.0040783 | synonymous-codon, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101611294 | TGGCCCTGACGGTCA[C/T]GGGTTTTGAAAATCC | 6468 |
rs751244951 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101643748 | CCCTCTTCCCTCCCA[C/T]GGTAAGTGCTTTCAG | 6468 |
rs751266824 | in-del | -/C | 2.86742e-05 | 0.00378633 | intron-variant, frameshift-variant, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101694637 | CCCCGGCCGCCGCCG[-/C]CATGGCCACCCCTGT | 6468 |
rs751270875 | snp | A/C | | | upstream-variant-2KB | FBXW4 | GRCh38.p7 | 10:101696083 | TATACATGGGACTTG[A/C]ATTTGTGGCTCGGGT | 6468 |
rs751272852 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101679608 | GGAATAAGAATATGC[A/G]TGGCTAGAAAGAACA | 6468 |
rs751296485 | in-del | -/AATGA | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101649541 | GAGTGCCTATTTCCC[-/AATGA]AAGAAATGTCCTCTG | 6468 |
rs751313675 | in-del | -/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101615179 | CTCGGCCTCTCACTG[-/T]TGGGGGGCGAGAGGG | 6468 |
rs751358219 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101666431 | TAGAAAGAAAAAAAA[C/T]TGAAAGGGAGTTGTG | 6468 |
rs751400544 | snp | A/C | 8.23961e-05 | 0.00641804 | synonymous-codon, intron-variant | FBXW4 | GRCh38.p7 | 10:101667972 | CCGGCCTGAGGCCAA[A/C]GGCCACACCTAGAAA | 6468 |
rs751436784 | snp | A/C | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101637037 | TAGCCAAGAGTTGGT[A/C]ATTATTCTACTTTTG | 6468 |
rs751488170 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101689422 | CCTGCTTCCACAGGT[A/G]TACTGTTTTATTTTG | 6468 |
rs751547465 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101667671 | ATTTCTGAGGTTAGA[C/T]GCTTAGGAAATTCGC | 6468 |
rs751547982 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101690668 | TTAGGAACAGCCAAA[C/T]TGAATGGGACTTGCC | 6468 |
rs751550164 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101671988 | TTTCTATATGGAGGT[A/G]TAATCACCAGAGGGT | 6468 |
rs751609130 | snp | A/G | 0.000115385 | 0.00759468 | synonymous-codon, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101611691 | GTAGGAGGAACCTGT[A/G]GCCAGCAGGTGGTTG | 6468 |
rs751671001 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101668863 | AAGGAAATCTCAGAC[A/G]TACAGGACTATCCCA | 6468 |
rs751713400 | snp | C/T | 1.64743e-05 | 0.00287 | missense, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101673512 | CTAACAATATGCGAG[C/T]TGGCCAGCACAAAGT | 6468 |
rs751719127 | snp | A/G | | | intron-variant, downstream-variant-500B | FBXW4 | GRCh38.p7 | 10:101625457 | GTGGGATGGGAGTCC[A/G]CCAGAGTCCTCTGAG | 6468 |
rs751732677 | snp | A/C | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101676659 | CAGTGATGCCAAAGC[A/C]ATCTAATGGAGAATG | 6468 |
rs751808894 | snp | A/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101635903 | TGCCTTGGAGCCCAC[A/T]TCCTCCCTACCCTGG | 6468 |
rs751814880 | snp | A/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101661791 | AGACCCAGAAGAAAC[A/T]ACCCACTCTGCCCCT | 6468 |
rs751837994 | snp | C/G | 3.29707e-05 | 0.00406008 | missense, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101673639 | CCTGGGATATGTACA[C/G]AGAATCATCCTCTAG | 6468 |
rs751911139 | in-del | -/A | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101616158 | ACCTTGAAATGCAAC[-/A]ATGGCTTTTGGAGAG | 6468 |
rs751942251 | snp | A/C | 1.65869e-05 | 0.00287979 | intron-variant | FBXW4 | GRCh38.p7 | 10:101673439 | GCAGGCAGAATGTCC[A/C]CGAAGTATAAGATGG | 6468 |
rs751990461 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101655177 | ATATATCTTGCAGAA[C/T]TGTCTGGTTATTGCC | 6468 |
rs752024010 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101610966 | CTCACTCTGTAGGCT[C/G]TCATGGCTCTAATAA | 6468 |
rs752028410 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101694128 | TAAGATGGCTAATTG[C/T]GAGGAGCGGCCCACC | 6468 |
rs752048620 | snp | C/G | 1.6476e-05 | 0.00287014 | intron-variant | FBXW4 | GRCh38.p7 | 10:101624719 | CTCCTGGACTGGAAG[C/G]CAGCATGGGCTCATG | 6468 |
rs752052989 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101669383 | CCCTGACACAAACTC[C/T]CTGGGAGGCAGATTC | 6468 |
rs752077820 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101684415 | ACAGGCGTGAGCCAC[C/T]GCGCCTGGCCTACCC | 6468 |
rs752128865 | in-del | -/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101643324 | GGAAAGCTGTGCTAT[-/G]GCTCAACTCCCAGGT | 6468 |
rs752131168 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101647968 | GATGATAACTTGCTC[A/G]GAATCTGCAGGGAGG | 6468 |
rs752232668 | snp | C/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101620099 | AGCACATACATAAAA[C/G]AGAAAATCCAGGCGC | 6468 |
rs752261498 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101658558 | TGGGTGGCAGGGGGG[A/G]ATGGTTTGAAATGAA | 6468 |
rs752277792 | snp | C/T | 1.64776e-05 | 0.00287028 | intron-variant | FBXW4 | GRCh38.p7 | 10:101667866 | CAGGACAAAACCACA[C/T]CCAAATATGTCTCCC | 6468 |
rs752364041 | snp | C/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101694048 | AGACTGGCTCCTCTG[C/G]GGCGAAGGAACCGGG | 6468 |
rs752367287 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101678331 | TCCTTAGCTTGCTCC[A/G]CTGCCCATACAAGGT | 6468 |
rs752381201 | snp | C/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101679357 | TACGCATATCAGTAA[C/G]TGCTCATAAAGAGCA | 6468 |
rs752402476 | snp | C/T | 1.6477e-05 | 0.00287024 | missense, intron-variant | FBXW4 | GRCh38.p7 | 10:101667962 | ACTGCCCCAGCCGGC[C/T]TGAGGCCAAAGGCCA | 6468 |
rs752422382 | snp | C/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101656849 | GTTACTTGAAATTCT[C/G]TTCTGCAAATTAAGA | 6468 |
rs752447256 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101692400 | AAAGTTGTAGACAAC[A/G]ATAGTAAGTTGAATT | 6468 |
rs752450889 | in-del | -/AAAAA | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101637700 | GCAAGATCCTGTCTC[-/AAAAA]AAAAAAAAAAAAAAA | 6468 |
rs752511220 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101613077 | TCCTGGTCTAGCTGG[C/T]CCCCAGCCCGGGGCT | 6468 |
rs752571607 | snp | A/C | 2.98851e-05 | 0.00386544 | intron-variant, utr-variant-5-prime, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101694670 | CCGCGATGTCGGCCC[A/C]AGCCTGACCCCCTCG | 6468 |
rs752577582 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101664974 | ACTGAGGCTGGGAGC[A/G]GGAATGACTTGCCTG | 6468 |
rs752615238 | snp | A/C | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101650175 | GAAGACAGCCTGCTC[A/C]TTGGTCCTTGGTGGC | 6468 |
rs752630394 | snp | C/G | 2.6236e-05 | 0.00362179 | intron-variant, missense, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101694576 | GCAGGCCCCGCGGCC[C/G]GGCGGGCAGCCGACT | 6468 |
rs752661901 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101666300 | TTAACTTCTCTCATC[A/G]TCAATATGCTAAGGA | 6468 |
rs752688245 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101680933 | TCTGTGGAGGAGAAT[A/G]GTATACTAATGCAAT | 6468 |
rs752715072 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101613402 | ATGAAGGAAAAGGGG[C/T]GCCCTCCAGGCCTGA | 6468 |
rs752742889 | in-del | -/A | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101647725 | GATAAGAAAGGTCAC[-/A]AAATTTGCAAATACA | 6468 |
rs752794076 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101622606 | GGTGGCAGGTACCTG[C/T]AGTCCCAGCTACTTG | 6468 |
rs752803295 | snp | C/T | 1.64751e-05 | 0.00287007 | missense, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101673506 | CCTGCACTAACAATA[C/T]GCGAGTTGGCCAGCA | 6468 |
rs752938308 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101636777 | TGTTTTTAGTAGAGA[C/T]GGGGTTTCACCATGT | 6468 |
rs752977404 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101689052 | TTTTAAAAAACCTGT[A/G]TACTTCCTCAGTGAC | 6468 |
rs752983821 | snp | A/G | 1.64776e-05 | 0.00287028 | synonymous-codon, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101672963 | GATGCCCCCTTTGCA[A/G]TCCACACAGTTCACC | 6468 |
rs753110940 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101683157 | GGAGCAGGTACCCCT[C/T]GGAATTCACCAGGGA | 6468 |
rs753146387 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101631083 | TTATCAAACTAAAGC[C/T]GAATAAGAACAAGAT | 6468 |
rs753158188 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101659765 | CTATTTCCAACAAGG[C/T]ACATGCAGAGCTAGT | 6468 |
rs753181940 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101671199 | AAGACAACAACAGAA[A/G]GGAGGGAAACCCAGG | 6468 |
rs753284187 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101661466 | CAGGGTGGAGGGCAC[C/T]GTACTGAGATTTAGC | 6468 |
rs753318722 | snp | G/T | 1.6486e-05 | 0.00287102 | intron-variant | FBXW4 | GRCh38.p7 | 10:101667844 | GTAAAATAAAAGCAT[G/T]ATTATACAGGACAAA | 6468 |
rs753323688 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101654241 | TTAATGATACAAAAG[C/T]AAATGTAAGGGAAGA | 6468 |
rs753336353 | snp | A/C | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101684326 | AGAGACAGAGTTTCA[A/C]CATGTTAGCCAGGAT | 6468 |
rs753427358 | snp | C/T | 0.000393623 | 0.0140234 | intron-variant, missense, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101694567 | CGCCAGAGCGCAGGC[C/T]CCGCGGCCGGGCGGG | 6468 |
rs753456420 | snp | A/C | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101658400 | AAATACAAAAATTAG[A/C]CAGGCGTGGTGGCAT | 6468 |
rs753536334 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101669116 | TTTTTAGAGTTTGTG[C/T]GTATGATGGGGGTGG | 6468 |
rs753539939 | in-del | -/G | 1.64727e-05 | 0.00286986 | frameshift-variant, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101673564 | CAGCAAAGACTCCCA[-/G]AGGCCGACGATTCAA | 6468 |
rs753591173 | snp | A/C | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101677017 | TGTATATCTGACAGG[A/C]ATTTGTACCGTGATG | 6468 |
rs753647701 | snp | C/T | 5.09014e-05 | 0.00504461 | intron-variant | FBXW4 | GRCh38.p7 | 10:101673068 | AGAGAAATAAGGAGC[C/T]GACCCCCAAGAACCA | 6468 |
rs753726212 | snp | C/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101622363 | GCACAGTCAATAAAA[C/G]AAAAAGTCAATAATT | 6468 |
rs753728282 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101656739 | AGCAGGCCCAGAGAC[A/G]AGCCTAAACACAAGT | 6468 |
rs753753563 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101680392 | GAAATGCTACAGGAA[A/G]GGAAAAAAGATTAAA | 6468 |
rs753771935 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101663922 | AAAAACAGGATTACC[A/G]GTGTTGAACAATAAG | 6468 |
rs753773093 | snp | C/T | 3.3036e-05 | 0.0040641 | missense, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101611322 | TCCAGGACGTGGAGG[C/T]TGTAAGACAGGGCAG | 6468 |
rs753773921 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101679138 | AACACCTGGCCTCAA[A/G]CAATCCTCCTGCCTT | 6468 |
rs753840521 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101613585 | AGCATGTCAGCAAAG[A/G]GCTTGAGGCAGACAA | 6468 |
rs753851128 | snp | A/C | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101641905 | GGCACAGTGGTTCAC[A/C]CTAGTAATCTCAGCA | 6468 |
rs753881830 | snp | A/G | 1.67764e-05 | 0.00289619 | missense, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101611394 | CTGCTGAGGGGAGTC[A/G]ACGTCAGCGGGAAGG | 6468 |
rs753934481 | in-del | -/TGAA | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101629836 | TGCTTATTGATTGAA[-/TGAA]TGAATGAATGAATGG | 6468 |
rs753951297 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101634915 | ACAAAAACTTCTACA[C/T]AACAGAAGACATCAA | 6468 |
rs753985811 | snp | G/T | 1.64781e-05 | 0.00287033 | synonymous-codon, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101672948 | GGAGCCACTCACAAT[G/T]ATGCCCCCTTTGCAA | 6468 |
rs754039642 | snp | A/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101649776 | CTCCCCAGGGCCACC[A/T]CATCTCAGCGGCCAG | 6468 |
rs754081012 | snp | C/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101687508 | ACTGAAGCTTCTGTA[C/G]AGTAACCACCACTCT | 6468 |
rs754088707 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101667539 | CTGTCACCTCCGAGA[A/G]GTGGTGAGAGGCCTC | 6468 |
rs754089137 | in-del | -/CAAA | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101675278 | CACTCAAGTAGGCAG[-/CAAA]CAGAGAGGGTGGGAA | 6468 |
rs754171049 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101685933 | TCCTTAAAATGTGTA[A/G]CATACCACATCTTCA | 6468 |
rs754181002 | snp | C/T | 1.89529e-05 | 0.00307832 | intron-variant | FBXW4 | GRCh38.p7 | 10:101612296 | GGACCAGGATTGGTG[C/T]AGGGCCCCCACCACC | 6468 |
rs754184210 | snp | A/C | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101672427 | GCAACAAACAACACC[A/C]CTCTCTCATCGTCTC | 6468 |
rs754232676 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101622465 | GGGTGCGGTGGCTCA[C/T]GCCTGTAATCCCAGC | 6468 |
rs754270681 | snp | A/T | | | upstream-variant-2KB | FBXW4 | GRCh38.p7 | 10:101696410 | TAGAATTACTTTTTG[A/T]TCTTAGCAAAACAAC | 6468 |
rs754291175 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101659604 | CTGATGGGAAGGAGA[C/T]CAGAGCAGGGATGTC | 6468 |
rs754297007 | snp | A/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101636542 | AGACATTCCTACATA[A/T]TTGATAATATTTTTC | 6468 |
rs754311941 | snp | A/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101620285 | TGTTCATTACCTTAA[A/T]CCTATTTTCTACATG | 6468 |
rs754326204 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101632630 | AAAACAAAAACTCTC[A/G]GTACAGTGGAATAAC | 6468 |
rs754333215 | snp | G/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101644022 | GAGAGACTGCAATTA[G/T]TCCCCCCATCCCACA | 6468 |
rs754429820 | snp | C/T | 3.29859e-05 | 0.00406102 | synonymous-codon, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101611712 | CAGGTGGTTGCCATC[C/T]GTCTGCAGGCAGTAC | 6468 |
rs754445770 | snp | C/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101617066 | CTGCTTAGGTTACCT[C/G]GTGGCAGAGTAGCCA | 6468 |
rs754456313 | snp | G/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101654332 | TAAATTTTCTAAAAA[G/T]CATGGAATTGTACAC | 6468 |
rs754463987 | in-del | -/GGGA | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101677692 | TTGGGAGGCCAAGAT[-/GGGA]GGATCACTTGAGCCC | 6468 |
rs754549994 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101668266 | TTCCACATTCCTCAG[C/T]GGAGACTTGACTGAG | 6468 |
rs754637281 | in-del | -/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101622123 | ATGTTGTTTTAAAAA[-/T]TTTGAAAAGACTGAC | 6468 |
rs754655810 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101641121 | CAGGCATGAGCCACC[A/G]CGCCCAGCCAACCCT | 6468 |
rs754656893 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101655557 | TGCCCAGCTGACCCT[C/T]CTCTTAGGTCATTTA | 6468 |
rs754699416 | snp | C/G | 0.000121706 | 0.00779989 | intron-variant, missense, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101694426 | TTGAGCGAGGCCCGG[C/G]CTATCCGGCGCCAGA | 6468 |
rs754729005 | snp | A/C | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101618626 | GTGCAGGGCTTGCCA[A/C]ACACACAGGGCAGCA | 6468 |
rs754756837 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101678239 | GCCCCTTACAGAGTA[C/T]GCCTTTGAAGAGAAT | 6468 |
rs754780390 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101626102 | GCCCTAGGCTGATAA[A/G]AAGGCCATACGAGCT | 6468 |
rs754822071 | snp | A/C | 5.20129e-05 | 0.00509939 | intron-variant, synonymous-codon, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101694569 | CCAGAGCGCAGGCCC[A/C]GCGGCCGGGCGGGCA | 6468 |
rs754836602 | snp | A/T | 1.69473e-05 | 0.0029109 | missense, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101612448 | GCCCCTGGGGGAAAG[A/T]CACTGCCCAAGTGTG | 6468 |
rs754871374 | in-del | -/A | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101682369 | AGACTACTGCTGAGG[-/A]ACAGTAAAAGATACT | 6468 |
rs754897658 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101642910 | CTACCTGTGATCTGG[A/G]GGTACGCACATACAT | 6468 |
rs754948263 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101633428 | CAGGGAGGGGAACAT[C/T]ACACACCAGGGCCTG | 6468 |
rs754952054 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101663933 | TACCGGTGTTGAACA[A/G]TAAGATGGGTAGAAG | 6468 |
rs754952097 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101680440 | AAAATTTTAACTAAC[A/G]CTGTAGATATAAGTT | 6468 |
rs754983244 | in-del | -/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101644412 | GCCAAATAGCTTTCT[-/G]GGAAGTGGAGACACT | 6468 |
rs755036155 | snp | A/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101648405 | ACACTAAATACCAGA[A/T]GATTTGATTGACTAG | 6468 |
rs755087990 | snp | A/T | | | upstream-variant-2KB | FBXW4 | GRCh38.p7 | 10:101695416 | CAGGAAGCGGCCATT[A/T]GGAGCACCTGCCCTC | 6468 |
rs755101614 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101664648 | AGGGAAACTTCCTGG[A/G]GCCAGAAGGAGCCCA | 6468 |
rs755116504 | snp | C/T | 1.65149e-05 | 0.00287353 | missense, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101611335 | GGTTGTAAGACAGGG[C/T]AGCATAGAGATGCTT | 6468 |
rs755228781 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101620625 | AACTGAGGCCATAGT[C/T]GTTTGTTTTGTTCTG | 6468 |
rs755248935 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101622470 | CGGTGGCTCACGCCT[A/G]TAATCCCAGCACTTT | 6468 |
rs755278239 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101671064 | TGTATTAGAAGCCTG[A/G]AGAAGCAGCTGTAGA | 6468 |
rs755296872 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101660155 | CAGGTCAGATAAGAG[A/G]AGAAAGAGCTCCTAC | 6468 |
rs755401365 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101657558 | AGAATCACTTGAACC[A/G]GGGAGGTGGAAGTTG | 6468 |
rs755456772 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101645331 | AAGATGAGAGGCCCA[C/T]GAAGATTCATGAAAC | 6468 |
rs755462524 | snp | C/T | | | upstream-variant-2KB | FBXW4 | GRCh38.p7 | 10:101696581 | TTACAGGTCAAATCC[C/T]GTTACAAAAAAATGC | 6468 |
rs755522422 | snp | C/T | 3.30721e-05 | 0.00406632 | missense, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101676410 | TGAGACACCTTCACT[C/T]GTTCCTTCACTGGGA | 6468 |
rs755550306 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101644041 | CCCCATCCCACATTC[A/G]TACCTGGGCTCTCCC | 6468 |
rs755561480 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101632659 | ACATAAGTTCATTCA[C/T]CCTATTGAATTTAAT | 6468 |
rs755583141 | snp | G/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101630860 | TCTGTCCAGCAAACA[G/T]CCCACCTTGCAGGTG | 6468 |
rs755584804 | snp | C/G | 3.29516e-05 | 0.00405891 | intron-variant | FBXW4 | GRCh38.p7 | 10:101624722 | CTGGACTGGAAGCCA[C/G]CATGGGCTCATGAAT | 6468 |
rs755604789 | snp | G/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101687952 | GGCAATATCTCTCTT[G/T]GCTGAGGAGAAACTG | 6468 |
rs755653241 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101681261 | GGCGTTGTAGTGGGC[A/G]TCTGCAATCCCAGCT | 6468 |
rs755672609 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101666724 | GTTCCAGAGAGCCTC[A/G]AAAGCAGAAGTCGGG | 6468 |
rs755725099 | snp | A/C | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101615620 | CAGGGCCCCCTGGCC[A/C]AAACCATCCTGCTGC | 6468 |
rs755740500 | snp | G/T | 0.00015722 | 0.00886484 | intron-variant, synonymous-codon, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101694413 | CGTGAAGCCGGAGTT[G/T]AGCGAGGCCCGGGCT | 6468 |
rs755777794 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101616860 | GGCCCCGATTGTAGA[C/T]AAGGAAACCAAGAGT | 6468 |
rs755873337 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101668045 | GGGAGGAGAGGTGCT[C/T]CGGGAGAGGTGACTG | 6468 |
rs755873375 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101649818 | GCCTTCCGATCCATA[C/T]GGAAAGTGAAGACAC | 6468 |
rs755875051 | snp | C/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101639174 | TGTGCCATCCCAGGA[C/G]TTGGTTCCAGTCTCT | 6468 |
rs755889975 | snp | A/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101675043 | GTGTTTCTTCCCCAG[A/T]CTCGTACAAGTGTCA | 6468 |
rs755891979 | snp | A/C | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101690831 | AAACGAAGCACAGTG[A/C]GTGTGTGTGCGTGTT | 6468 |
rs755910383 | snp | C/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101689566 | AGAACAAATAAGTGA[C/G]TGTCCTCCCTGGGTA | 6468 |
rs755936627 | snp | A/G | 0.000446063 | 0.0149276 | synonymous-codon, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101611318 | AAAATCCAGGACGTG[A/G]AGGTTGTAAGACAGG | 6468 |
rs755969920 | snp | A/C | 0.000249018 | 0.0111556 | intron-variant | FBXW4 | GRCh38.p7 | 10:101676448 | CATCCTATGTCCAGA[A/C]AGAACAGATAATCCA | 6468 |
rs755979659 | in-del | -/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101617649 | GGCCAGGCAGCCCAC[-/T]TTGTACTGCTAACAA | 6468 |
rs755986108 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101676952 | ATCCAAAACATCTGC[C/T]CACCAAAATGAATAC | 6468 |
rs756085311 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101676919 | AAAATAAAAATCCAG[C/T]AAATCAGACTTCATC | 6468 |
rs756091988 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101646718 | GGAGAGAGCACTTTT[C/T]ACTACCCAGCAAATA | 6468 |
rs756109076 | snp | A/G | | | synonymous-codon, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101673544 | GCAAACGTCCTCATC[A/G]TGCCCAGCAAAGACT | 6468 |
rs756138293 | snp | G/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101624728 | TGGAAGCCAGCATGG[G/T]CTCATGAATCTCTTA | 6468 |
rs756145527 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101611124 | TCTCTGGTAAGCTCC[A/G]AAGTCCCAGGAGTCA | 6468 |
rs756161285 | in-del | -/ATA | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101656251 | ACTTGCTATGCCAAC[-/ATA]ATAATCAAAGTGGTG | 6468 |
rs756162964 | snp | A/C | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101663798 | CCCAGGCACGCCTCC[A/C]GCATCTCATTCCTGG | 6468 |
rs756320301 | in-del | -/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101649618 | TTCCTTTGGGATTTA[-/G]GCCCCTCAAAGACCT | 6468 |
rs756331921 | snp | G/T | 1.64982e-05 | 0.00287208 | intron-variant | FBXW4 | GRCh38.p7 | 10:101668000 | AAACAGGAGAGGAGA[G/T]GCTCTCGTTGGCATT | 6468 |
rs756376007 | snp | A/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101671002 | AAACTCCCCAAAAAT[A/T]GATGGTTACAGGCAA | 6468 |
rs756387245 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101633310 | ATAAAGGGGACATCA[A/G]TGAAGCTGGAAACCA | 6468 |
rs756388426 | snp | C/T | 3.29815e-05 | 0.00406075 | missense, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101611647 | AGGCAGGCCCTTTGA[C/T]GCCGGTCCCACAGCC | 6468 |
rs756428751 | snp | G/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101648140 | TCCTGCGATTTGGGT[G/T]TTTTTGTTTGTTTGT | 6468 |
rs756489272 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101659334 | GATAAGTCATGGATG[A/G]TTTGAGTGGCTTAGT | 6468 |
rs756493872 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101619103 | CCAAACTCCAGGCTC[A/G]GGCAGGATGGCTTTG | 6468 |
rs756510419 | snp | C/T | 1.64904e-05 | 0.00287139 | missense, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101611707 | GCCAGCAGGTGGTTG[C/T]CATCTGTCTGCAGGC | 6468 |
rs756524324 | in-del | -/AGAA | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101617849 | AAAAGTTAAGGGGGG[-/AGAA]AGAAAGAAAGAAATT | 6468 |
rs756549857 | snp | C/T | 3.29451e-05 | 0.00405851 | missense, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101673549 | CGTCCTCATCATGCC[C/T]AGCAAAGACTCCCAG | 6468 |
rs756587405 | snp | A/C | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101642636 | CTCCCCACTGCCAGT[A/C]TGTAGGCACCAAATT | 6468 |
rs756597159 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101629541 | CACCTACCTTGGCCT[C/T]GCAAAGTTCTGGGAT | 6468 |
rs756682581 | snp | C/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101663687 | TCTTGGGAAGTTGCT[C/G]AGAATTCCATGTGAC | 6468 |
rs756691609 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101643972 | CCCCGCAAAGCCTAA[C/T]TGACTTACTGAAGTT | 6468 |
rs756708882 | snp | G/T | | | upstream-variant-2KB | FBXW4 | GRCh38.p7 | 10:101696241 | TCTACATCTTAACAC[G/T]CATTTTCAGGGAGCA | 6468 |
rs756746754 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101627958 | CCCAGGTGATTTAAC[C/T]CAAACAAAATGCTGT | 6468 |
rs756783062 | snp | G/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101658472 | ATTGCTTGAACCCAG[G/T]AGGCGGAAGTTGCAG | 6468 |
rs756816617 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101679715 | TTTTACATATTTTCT[A/G]ATTTTTCTTTTTCCT | 6468 |
rs756892344 | snp | C/T | 0.000147091 | 0.00857461 | intron-variant | FBXW4 | GRCh38.p7 | 10:101612315 | GCCCCCACCACCTGT[C/T]CTCCCTGCCCAGCAC | 6468 |
rs756898860 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101665552 | GACCTTAGCAGAGGG[C/T]CTGGCACAGAGCAGA | 6468 |
rs756953810 | snp | C/T | 1.64827e-05 | 0.00287073 | splice-acceptor-variant, intron-variant | FBXW4 | GRCh38.p7 | 10:101667982 | GCCAAAGGCCACACC[C/T]AGAAACAGGAGAGGA | 6468 |
rs757008464 | snp | A/C | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101652858 | CTTCTCCAGGCTCCT[A/C]GTTTTCCTTCTGCCT | 6468 |
rs757031643 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101649599 | GCTGCTTCTTACTGA[C/T]GGGTTCCTTTGGGAT | 6468 |
rs757074354 | snp | A/C | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101688148 | TCTCTAACTCCTATG[A/C]TTCTTTGACCTCCAA | 6468 |
rs757074661 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101668885 | ACTATCCCAAGACAG[C/T]AGCAACAGAGGGATC | 6468 |
rs757084025 | in-del | -/A | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101665350 | GGAGCTGACAGAGTG[-/A]AAAGAATCATCCCAA | 6468 |
rs757107522 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101639003 | TATCTATGTACACAA[C/T]AGGTAAAGCCTATCC | 6468 |
rs757138834 | snp | C/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101666486 | GGCTCCATGGGGTGA[C/G]GAGAAAGAAGCTGAA | 6468 |
rs757273683 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101624221 | AACACCTTTCCATCT[C/T]ATTTTTGTAACTTCC | 6468 |
rs757274564 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101637045 | AGTTGGTAATTATTC[C/T]ACTTTTGTATATTTT | 6468 |
rs757302919 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101676838 | TGTCAGAAGAAAATA[C/T]ATAAAAACATCTCTC | 6468 |
rs757311059 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101674533 | CCCTTATTCTGTTAG[A/G]GCTAAGGGGTCATTT | 6468 |
rs757513556 | in-del | -/AT | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101681398 | GTCTCAAAAAAAAAA[-/AT]AATAATAATAATAAT | 6468 |
rs757520320 | snp | A/C | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101632343 | TTGCTCCCTGCCCCC[A/C]AACTGCAACTCCAAC | 6468 |
rs757527176 | snp | C/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101646642 | GGCCAGCCCTTTTGG[C/G]ACCAGCTTCCTTCTT | 6468 |
rs757592792 | snp | G/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101636488 | TGTGCCCAAGTGCTG[G/T]TCTAAGCACTTTCTA | 6468 |
rs757619353 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101661916 | CCTGAGTTTTTCCTC[A/G]AGTTATCAAGGTCAA | 6468 |
rs757619485 | snp | C/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101645734 | AGAGAATCAAGTCTT[C/G]AATTCATTTTTTTTA | 6468 |
rs757627045 | snp | G/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101683407 | CTTCTCTCTCAGCTT[G/T]CCGGCACTTAGTAAC | 6468 |
rs757647101 | in-del | -/GACT | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101622906 | AAATGATACAGAGAA[-/GACT]GACTGGCATGGCTCT | 6468 |
rs757773525 | snp | C/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101618859 | CTGTGCTCAGGGCAC[C/G]AGTGCTAGGTCCATC | 6468 |
rs757777028 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101656920 | ACCCCACCTGTCCCC[C/T]CTACACTTTTCTGTG | 6468 |
rs757798790 | snp | G/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101669727 | CAAATTCAAAACAGA[G/T]CCATCCCTGGAAAAG | 6468 |
rs757825418 | snp | C/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101655268 | ATACTCATTGACAAC[C/G]TAATGCAATTTAAAA | 6468 |
rs757857596 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101641229 | TTAATTAAAAGCATG[C/T]ACAATTGGATAGGAG | 6468 |
rs757875441 | snp | C/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101622929 | ATGGCTCTTATGCAA[C/G]AATGACATGCAAATA | 6468 |
rs757945220 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101655678 | CAGCTGCAACAAGGC[A/G]GAAAATAGCAGGAGA | 6468 |
rs758040854 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101642354 | CCAAGAGTTCAAGAC[C/T]AACCTGGCCAACATA | 6468 |
rs758052781 | snp | C/T | 3.86795e-05 | 0.00439753 | intron-variant | FBXW4 | GRCh38.p7 | 10:101673712 | TAAAAGTCATCAAGA[C/T]ACAGTATGAAAACTC | 6468 |
rs758089683 | snp | A/C | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101627791 | GGCCAAGCTTCCATG[A/C]ATGGACTTAAAATAC | 6468 |
rs758149976 | snp | C/G | 1.64749e-05 | 0.00287005 | missense, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101624770 | CCCAGATTCTCAGGG[C/G]TGAGAAGTGCCCGCA | 6468 |
rs758190393 | snp | A/C | 3.29549e-05 | 0.00405911 | intron-variant | FBXW4 | GRCh38.p7 | 10:101667867 | AGGACAAAACCACAT[A/C]CAAATATGTCTCCCT | 6468 |
rs758230499 | snp | C/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101613121 | GATCACAGCCCCCAG[C/G]CTGTGGGGCTCCAGC | 6468 |
rs758248012 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101679376 | TCATAAAGAGCAATT[A/G]TAATTCTTATATTTC | 6468 |
rs758306463 | snp | C/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101646593 | CTGTGAGGCAGCCGG[C/G]AAGGCCAGGGGACGC | 6468 |
rs758309669 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101635520 | TATATAGTCAAAAGA[C/T]TAATACTGAGAATAT | 6468 |
rs758311392 | in-del | -/AG | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101668859 | CAGAAAGGAAATCTC[-/AG]ACGTACAGGACTATC | 6468 |
rs758359860 | snp | A/G | 3.38713e-05 | 0.00411516 | missense, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101611403 | GGAGTCGACGTCAGC[A/G]GGAAGGCCTGGAAGG | 6468 |
rs758361929 | snp | A/C | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101620975 | CAGAAGAGGCCATTC[A/C]AAGATTACCCAACAT | 6468 |
rs758387288 | snp | C/G | 8.06961e-05 | 0.0063515 | intron-variant, missense, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101694585 | GCGGCCGGGCGGGCA[C/G]CCGACTCCCGAGCCG | 6468 |
rs758396006 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101650246 | TGCCTCCACTTAGGC[C/T]CTAGTTCCTAGGGAC | 6468 |
rs758409178 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101687967 | TGCTGAGGAGAAACT[A/G]GAGACAACCTCCAGC | 6468 |
rs758455137 | in-del | -/A | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101626226 | TAGAGTGGGAGTGCC[-/A]AAACAGTCACTGTGC | 6468 |
rs758487683 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101689228 | CTCATCTCACAGACT[A/G]TGAAGACATTGGGTT | 6468 |
rs758509943 | snp | A/G | 1.65916e-05 | 0.00288019 | intron-variant | FBXW4 | GRCh38.p7 | 10:101611611 | CATGCTGGAGAAGAG[A/G]TGGGCAGGACACTTA | 6468 |
rs758543533 | snp | A/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101673291 | CCAGCTTCACTTTTC[A/T]TTAGAAGCTCTTCCT | 6468 |
rs758585336 | snp | C/G | 1.724e-05 | 0.00293594 | intron-variant | FBXW4 | GRCh38.p7 | 10:101673082 | CCGACCCCCAAGAAC[C/G]AATTATTCTTTCTGT | 6468 |
rs758736780 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101658917 | TCTTCTTAAATATAC[A/G]AGTATTATCATGACA | 6468 |
rs758755054 | snp | C/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101682108 | CTTTACATAAGTATA[C/G]GTAGTAGATAATATC | 6468 |
rs758777023 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101691612 | GTAGATTCATTCCCA[A/G]TATCTCTCTTTTAGA | 6468 |
rs758881399 | snp | A/C | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101615799 | CAGGGACAGGCCCTG[A/C]GTGCTAAGCTGGACT | 6468 |
rs758882720 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101650984 | GCCGGCAAATCTCCC[A/G]CCTGGGCCCTGAGTT | 6468 |
rs758950847 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101683231 | CCATATGGTTACTAA[C/T]GTAAAGTGAGGGTGC | 6468 |
rs758993950 | snp | A/G | 6.59424e-05 | 0.00574168 | intron-variant | FBXW4 | GRCh38.p7 | 10:101667845 | TAAAATAAAAGCATT[A/G]TTATACAGGACAAAA | 6468 |
rs759047291 | snp | C/T | 6.59033e-05 | 0.00573997 | missense, intron-variant | FBXW4 | GRCh38.p7 | 10:101667958 | AAGCACTGCCCCAGC[C/T]GGCCTGAGGCCAAAG | 6468 |
rs759169990 | snp | C/G | 6.01323e-05 | 0.00548293 | intron-variant, utr-variant-5-prime, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101694665 | TGTCCCCGCGATGTC[C/G]GCCCAAGCCTGACCC | 6468 |
rs759201620 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101656742 | AGGCCCAGAGACGAG[C/T]CTAAACACAAGTACA | 6468 |
rs759208092 | snp | A/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101657986 | TGGTATGAGGAAAAT[A/T]CCCTAGCTCTTAATC | 6468 |
rs759234599 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101693832 | CCCCCTTTTTCGTGT[C/T]GCTCTGCCTATATGA | 6468 |
rs759295712 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101670760 | GCCCAGGCTCATTAA[A/G]AACATAAGCTACCAG | 6468 |
rs759324277 | snp | A/C | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101631449 | AGCACTGTTACAACT[A/C]CTAAAAAAAAGAGCC | 6468 |
rs759364273 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101641995 | AACATGGTGAAACCC[C/T]GTCTCTACTAAAATT | 6468 |
rs759367323 | snp | A/G | 3.29511e-05 | 0.00405887 | synonymous-codon, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101673499 | TTACCCTCCTGCACT[A/G]ACAATATGCGAGTTG | 6468 |
rs759434998 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101679211 | TGCATCTGGCCAGCT[A/G]AATACTATTTTTAAA | 6468 |
rs759540334 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101628600 | TGAAGTTGGTCCCTC[C/T]GCTTCCTAAAGGAAT | 6468 |
rs759542065 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101644800 | GCTGAGCTGCCCATA[A/G]CACAGGCCACTGCTC | 6468 |
rs759542987 | in-del | -/CAG | 1.95353e-05 | 0.00312526 | intron-variant | FBXW4 | GRCh38.p7 | 10:101673714 | AAAGTCATCAAGATA[-/CAG]TATGAAAACTCAACT | 6468 |
rs759555185 | snp | C/T | | | upstream-variant-2KB | FBXW4 | GRCh38.p7 | 10:101696012 | TTAATATTTTGGATA[C/T]GCTGTATTGGGCTAA | 6468 |
rs759564443 | in-del | -/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101648925 | AAGGAATGAGGCTTC[-/T]TAAGTGCCCTCTCAC | 6468 |
rs759679770 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101680594 | GGAGGAAACATCCCC[C/T]AAGAATAGTTTACAG | 6468 |
rs759702607 | snp | A/C | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101614700 | GCCAATGAAAAGATA[A/C]AATTTCTTTTGCCCC | 6468 |
rs759704117 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101613640 | CAGATGTCAGCTCTC[A/G]TCCTTCCACCTCACT | 6468 |
rs759721444 | snp | A/C | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101653649 | CTCTGATTTCCTGTC[A/C]ATAACCCCAGTAGTT | 6468 |
rs759735596 | snp | A/C | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101630322 | TTTTTGATGGGCTGC[A/C]AGTGGGCTCCCGAAC | 6468 |
rs759750051 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101613227 | TCCCTCCGTGACCGC[A/G]GCAGTGGGCAGACCC | 6468 |
rs759792558 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101665594 | TGTTAGCTGCTAGTA[A/G]TAGTGGCAGTCATGT | 6468 |
rs759813864 | snp | A/C | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101652200 | ATCCGAGGACTTGAA[A/C]GTTTTTAGTTATATC | 6468 |
rs759817124 | snp | A/G | 1.78182e-05 | 0.00298476 | intron-variant | FBXW4 | GRCh38.p7 | 10:101612514 | GAGAGGCTGCTCCAC[A/G]TGGGTCATACACATT | 6468 |
rs759893936 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101638272 | CTAGAATGCTGCAGT[C/T]AAAAAGAACATGGTA | 6468 |
rs759940015 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101661124 | GTCTGGACACATCAA[C/T]TCTGTATCCACAGTA | 6468 |
rs759941552 | snp | A/C | 0.00033151 | 0.0128703 | intron-variant, missense, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101694391 | CTTACAGGTCGGTGC[A/C]GAGCCGCGTGAAGCC | 6468 |
rs759945810 | snp | C/T | | | intron-variant, downstream-variant-500B | FBXW4 | GRCh38.p7 | 10:101625214 | AACAGGTTGCTGGGG[C/T]TGGAAGGTGCTGCCC | 6468 |
rs759958216 | snp | C/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101635425 | GACTCACCCCCCTCC[C/G]ACCCCCGAGGCTATG | 6468 |
rs759980303 | snp | A/G | 0.000116522 | 0.007632 | synonymous-codon, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101612392 | CATAGCCACAGGACA[A/G]CAGTGTGAAAGGGGA | 6468 |
rs759994322 | snp | A/G | 0.000112771 | 0.00750819 | intron-variant, missense, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101694466 | AGCTGGTGAAGCGCC[A/G]CAGCCAGCGGCACAC | 6468 |
rs760092127 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101624007 | CTGATGGAACAAACA[A/G]TTCTGTACCTCAATT | 6468 |
rs760190880 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101675714 | ATCAACAAGGAGCAA[C/T]TTTTTGGTAGAGAGT | 6468 |
rs760234375 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101693106 | GTGGTAAAAGAGATG[C/T]AAAATAACACAACTT | 6468 |
rs760247558 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101637657 | GTGAGCCAAGATCAT[A/G]GCACTGTACTCCAGC | 6468 |
rs760311577 | snp | G/T | | | downstream-variant-500B | FBXW4 | GRCh38.p7 | 10:101610473 | ACCCACAGGTGACCC[G/T]CCATACCCCAAAGGG | 6468 |
rs760311745 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101641109 | GTGCTGGGATTACAG[A/G]CATGAGCCACCGCGC | 6468 |
rs760403162 | snp | G/T | 5.36092e-05 | 0.00517704 | intron-variant | FBXW4 | GRCh38.p7 | 10:101611454 | GAGCTTTCCAAGTGG[G/T]ACATGGGTGTGCCCT | 6468 |
rs760405993 | snp | C/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101685490 | TCTATCAGACACTAA[C/G]CCAAAATATTGCCCA | 6468 |
rs760414823 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101684273 | GGACTACAGGCGCCC[A/G]CCACCATGCCCGGCT | 6468 |
rs760461720 | in-del | -/C | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101611978 | ATGGCCCAGACGACA[-/C]AGCAGATTATGCCTG | 6468 |
rs760482820 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101670595 | CTCCCTGGCCAGGTA[C/T]GCACATCTCTTCTCA | 6468 |
rs760562724 | snp | G/T | 1.6691e-05 | 0.00288881 | missense, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101611389 | CAGGGCTGCTGAGGG[G/T]AGTCGACGTCAGCGG | 6468 |
rs760564679 | snp | A/T | 3.2962e-05 | 0.00405954 | intron-variant | FBXW4 | GRCh38.p7 | 10:101673484 | AGAAACCTATAGCAC[A/T]TACCCTCCTGCACTA | 6468 |
rs760570800 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101669045 | TGATGGAGTAGGGGT[A/G]GTCCTGCCTTCTTAA | 6468 |
rs760629299 | snp | A/C | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101619834 | TAGTGGTCTTGATGG[A/C]ATGAGGGGCTGAGGG | 6468 |
rs760629811 | snp | A/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101641833 | AGATGTTACATAAGA[A/T]CTCTATAAACATATC | 6468 |
rs760653899 | snp | C/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101692181 | ACAGATTACTAGACT[C/G]TATCAAAAAGTAACA | 6468 |
rs760658097 | in-del | -/AAT | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101681721 | ACTCCGTCTCAAAAT[-/AAT]AATAATAATAATAAT | 6468 |
rs760756788 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101656664 | ATGGCCATTGTTCTA[A/G]AAGCTGGATTATGGC | 6468 |
rs760759634 | snp | C/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101627176 | ATTACAGGTGTGAAC[C/G]ACTGGCGCTCAGCCT | 6468 |
rs760765362 | snp | C/T | 1.66701e-05 | 0.002887 | missense, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101612385 | TAGGTGTCATAGCCA[C/T]AGGACAGCAGTGTGA | 6468 |
rs760774073 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101693669 | TTCCCCCAATTCCCT[A/G]CATGTTTTTTCCTTC | 6468 |
rs760789323 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101649513 | AGGAAAAAGGAGGGG[C/T]GGGTATTGCTGGGAG | 6468 |
rs760799090 | snp | A/C | 1.81803e-05 | 0.00301494 | intron-variant | FBXW4 | GRCh38.p7 | 10:101611815 | TTTAGGGTACCCTCC[A/C]CCTCTACCCCAGCTT | 6468 |
rs760811775 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101628466 | GCTCTTGGGTACTGT[A/G]CTGTCTAGCACAGTG | 6468 |
rs760831308 | in-del | -/TAA | 0.000133187 | 0.00815939 | intron-variant | FBXW4 | GRCh38.p7 | 10:101672884 | ATAGACAGGAGGGAG[-/TAA]TAATAGTATGTAAGG | 6468 |
rs760873101 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101664793 | AGGAGTTCATAATCA[A/G]CATGGGTGATAAAGT | 6468 |
rs760882447 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101613503 | ACACTTCACAGGGAT[A/G]TCCAGGTAAGAGGCC | 6468 |
rs760900810 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101612566 | CAGACCTTGGGGAAA[C/T]GTTCTCTTTCCTCAG | 6468 |
rs760937584 | snp | A/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101683056 | CTCTGAAAACAGGTA[A/T]CCCTCCATCCCTGTG | 6468 |
rs760952045 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101680285 | AGAGCAGAGATAATT[C/T]CCCAATTGAAATGGG | 6468 |
rs760956768 | snp | C/T | 1.65217e-05 | 0.00287412 | stop-gained, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101676388 | GCAGCGCCCCAGTCT[C/T]CAGTTCTGAGACACC | 6468 |
rs761075863 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101667405 | CTTTGTTTGAGGACC[C/T]AGCTGGATCTGGGCC | 6468 |
rs761126667 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101688560 | ACTCATTTTTAGAGA[A/G]AGCTCAAATATTTAC | 6468 |
rs761207534 | snp | G/T | 0.000646094 | 0.0179619 | utr-variant-3-prime, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101611279 | GCCCAGAGGCAGGGG[G/T]GGCCCTGACGGTCAT | 6468 |
rs761262125 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101638006 | GTACACACTGTTTGC[A/G]GGTATAGAACCTGAT | 6468 |
rs761278553 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101636311 | GAGCCAAGATTGAGA[C/T]TGAGCCACTGCACTC | 6468 |
rs761288374 | snp | G/T | 0.000226014 | 0.0106281 | intron-variant, missense, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101694399 | TCGGTGCCGAGCCGC[G/T]TGAAGCCGGAGTTGA | 6468 |
rs761394223 | snp | C/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101670734 | AGGAAATGAAGGAAT[C/G]GTTAGTACCAGCCCA | 6468 |
rs761413112 | snp | A/G | 6.67234e-05 | 0.00577557 | synonymous-codon, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101611387 | CACAGGGCTGCTGAG[A/G]GGAGTCGACGTCAGC | 6468 |
rs761427909 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101646271 | CAGGACAAATTTAAC[C/T]TGGCCAGGGCCTCAG | 6468 |
rs761458976 | snp | C/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101623750 | ACTCAGCAATAAAGA[C/G]GAATGCACTATTGAT | 6468 |
rs761498351 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101630613 | TCACAAAAACTCACT[C/T]GGTGAGGGGAAGCCA | 6468 |
rs761499239 | snp | A/C | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101687425 | AAGGGGAGACCACAA[A/C]ATCAACAGCGTACCC | 6468 |
rs761512194 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101661001 | AGTGGAAGGTGGGTA[C/T]TGAGGAGGAAGGGAG | 6468 |
rs761514890 | snp | A/G | 1.65798e-05 | 0.00287917 | synonymous-codon, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101611303 | CGGTCATGGGTTTTG[A/G]AAATCCAGGACGTGG | 6468 |
rs761516117 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101645201 | TGGCTAGTCTCAATA[C/T]CCACAGTTCAGATGT | 6468 |
rs761611464 | in-del | -/CC | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101613851 | GCAGCACCCCTGCTA[-/CC]AGCCTCCTCAGGGAA | 6468 |
rs761634050 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101667712 | TTATCTCAATCCCAC[A/G]CATATATGAAGTGGC | 6468 |
rs761642562 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101684090 | TGCCTCAGCCTCCCA[A/G]GTAGCTGGGATTACA | 6468 |
rs761668355 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101616671 | CACTAGGGCAACCAG[A/G]CTGTTTTGGCGGCAG | 6468 |
rs761678330 | in-del | -/C | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101619881 | AAAGGGGTCCAGGTT[-/C]TGTGAGAAGCAGCAT | 6468 |
rs761705961 | snp | C/T | 3.30218e-05 | 0.00406323 | intron-variant | FBXW4 | GRCh38.p7 | 10:101672910 | TAAGGGGGAGACCAC[C/T]TCACCTTGGCCGTCC | 6468 |
rs761730326 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101690238 | TCTTGCATTCAGTCT[A/G]CATTATCAAGTGACA | 6468 |
rs761804866 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101618194 | CACTCATATCCTGTG[C/T]TCAGTTCAGGATACC | 6468 |
rs761815951 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101620617 | CCAGGAAGAACTGAG[A/G]CCATAGTTGTTTGTT | 6468 |
rs761825104 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101691921 | TACAAGAGTAGAGTA[A/G]TCTTCTACATTCAGT | 6468 |
rs761840833 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101657257 | ATTTTACTAGGGCAC[C/T]CCAGAGGCAGAGGGA | 6468 |
rs761887989 | snp | A/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101653328 | ACAACATAAACCATT[A/T]AACTGCTTCAATCTG | 6468 |
rs761898409 | snp | A/G | 1.69198e-05 | 0.00290854 | intron-variant | FBXW4 | GRCh38.p7 | 10:101611777 | CACATTTCCTGTCCA[A/G]GAAGAGGAGAAGCAG | 6468 |
rs761901213 | snp | A/G | 1.65269e-05 | 0.00287457 | stop-gained, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101676372 | GCAGAATCCCCTCTC[A/G]GCAGCGCCCCAGTCT | 6468 |
rs761914589 | snp | C/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101690727 | AGTTTGTGTTTCTGA[C/G]AATCAAGAGGCTCTT | 6468 |
rs761929220 | in-del | -/AG | 3.29489e-05 | 0.00405874 | frameshift-variant, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101624766 | AGGTCCCAGATTCTC[-/AG]GGGTGAGAAGTGCCC | 6468 |
rs761958895 | snp | A/C | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101641680 | GTGTGTCCCCCCAAA[A/C]CCTCTCACTCTCTTT | 6468 |
rs761981226 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101675981 | GTAAAATAAGATGAA[C/T]TGAAACCTTGATTTA | 6468 |
rs762007625 | snp | A/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101677814 | AGAGAAAAGAAATAC[A/T]TCAAATGATACACAA | 6468 |
rs762028531 | in-del | -/C | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101664610 | CCTACTGAGTCCCCA[-/C]CTCAAGAAGACTGCA | 6468 |
rs762039666 | snp | A/G | | | intron-variant, downstream-variant-500B | FBXW4 | GRCh38.p7 | 10:101625515 | CACGAGAAGGAGCAG[A/G]CTGACCCTGTTGCCC | 6468 |
rs762072851 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101678866 | CAGGCAGAAAGAAGA[C/T]ACCTAATTCACTTTT | 6468 |
rs762080895 | snp | C/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101680101 | TAATATTCAAATACT[C/G]ATTAAAATAGTAATA | 6468 |
rs762196847 | snp | C/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101664671 | GGAGCCCAGGAAAAG[C/G]GTACAGACTTGACAG | 6468 |
rs762201748 | snp | C/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101612292 | GGAAGGACCAGGATT[C/G]GTGCAGGGCCCCCAC | 6468 |
rs762271297 | snp | C/T | 1.64757e-05 | 0.00287012 | missense, intron-variant | FBXW4 | GRCh38.p7 | 10:101667946 | TGGATGGTGTGTAAG[C/T]ACTGCCCCAGCCGGC | 6468 |
rs762350589 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101685735 | AATTCTTTAATGTAC[C/T]ATCAAAAATTCTAAC | 6468 |
rs762381477 | snp | A/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101672320 | TGATCCAGATGTGGA[A/T]GAGTCCATGAAGCCA | 6468 |
rs762393958 | snp | C/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101687271 | ATAATACCCCCTTCG[C/G]ACTGCTCCCAACAGC | 6468 |
rs762470344 | snp | C/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101649197 | TGAACACCCCCTATA[C/G]ATACATCTAATTTGT | 6468 |
rs762481470 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101663079 | GCACACAGGACATGG[A/G]AACAGGCTAGGGAAC | 6468 |
rs762505301 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101636124 | GGAGGCTGAGGTGGG[C/T]GGATCAGTTGAGGTC | 6468 |
rs762537720 | in-del | -/AAAT | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101620883 | AAGAGAATAACAGTC[-/AAAT]AAATGGTGCCTTAGA | 6468 |
rs762559377 | snp | G/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101659308 | AACACTCAGCCATCT[G/T]GAACCCTGCAGATAA | 6468 |
rs762563151 | in-del | -/TCTC | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101652067 | TCCCTCAATAAAATT[-/TCTC]TCTCTGATTCCTTCT | 6468 |
rs762600287 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101680968 | TATACTGCCACTAGA[A/G]ATGACAAATGTGAGG | 6468 |
rs762632036 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101643604 | ACAAGGAAACTCCAC[A/G]CAGATCCTGTAGACA | 6468 |
rs762642521 | snp | G/T | 1.64776e-05 | 0.00287028 | synonymous-codon, intron-variant | FBXW4 | GRCh38.p7 | 10:101667963 | CTGCCCCAGCCGGCC[G/T]GAGGCCAAAGGCCAC | 6468 |
rs762650396 | snp | G/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101673957 | GAGAATATTTAATAT[G/T]TCAATTACTGGCTAC | 6468 |
rs762675680 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101683850 | ATTTGGAAGGAAACT[C/T]AGGAAAGGAAAGTGT | 6468 |
rs762712140 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101627864 | TCCCTTGAGACTCAC[A/G]GGATAAAGTGCTTTG | 6468 |
rs762724257 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101658204 | GAAGTCCTGGGGACC[A/G]GGACTCTGGTACATA | 6468 |
rs762785895 | snp | C/G | 1.64844e-05 | 0.00287087 | missense, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101611687 | CGTAGTAGGAGGAAC[C/G]TGTGGCCAGCAGGTG | 6468 |
rs762876951 | snp | A/C | | | upstream-variant-2KB | FBXW4 | GRCh38.p7 | 10:101696063 | ACTACTAGAAAATTT[A/C]AAATTATACATGGGA | 6468 |
rs762924902 | snp | A/C | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101667431 | GGGCCCCAAGCCTCT[A/C]CTGATGACTTAAGAC | 6468 |
rs762935120 | snp | A/C | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101649224 | TTGTTTCTATGATTT[A/C]ATCTCTCTCCTCCAT | 6468 |
rs762971344 | snp | C/G/T | 3.29507e-05 | 0.00405887 | synonymous-codon, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101673508 | TGCACTAACAATATG[C/G/T]GAGTTGGCCAGCACA | 6468 |
rs762984470 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101686534 | CTCTAAGTGAGTCAT[A/G]AATTAGGCACTAGCA | 6468 |
rs762984636 | snp | A/C | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101614971 | AGGGAGAGATTGGCC[A/C]GACAATAGCCCCAAA | 6468 |
rs762988460 | snp | A/T | 3.32618e-05 | 0.00407797 | missense, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101611758 | GGCTCCTCCCACTCC[A/T]TGACACATTTCCTGT | 6468 |
rs763079350 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101624142 | AATCTGAATAAAGGT[C/T]CATGGATGGTACCAG | 6468 |
rs763128561 | snp | A/C | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101690528 | CGGGCAAGAGGCCTA[A/C]AGGGAAGCAAATTAT | 6468 |
rs763172317 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101638671 | ATGGTAATCAAAATA[C/T]TCATTTTGAAGTTAC | 6468 |
rs763174575 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101655087 | CTCCTACCTCAGCCT[C/T]CCAAAGTGCTGGGAT | 6468 |
rs763207718 | snp | C/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101671377 | AATTTTAGAAGGAAG[C/G]ACTTATTTTAGATCT | 6468 |
rs763337447 | snp | C/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101647801 | CTTACTTCAGGCTTT[C/G]ATTTCTCCACAGTAC | 6468 |
rs763340084 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101677614 | TATACAAGTTTATAT[A/G]CATTTGTCAGAAATG | 6468 |
rs763361856 | snp | C/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101611884 | CATTCCGGGATGGAA[C/G]AGAAAGAAGCCTAAA | 6468 |
rs763370651 | snp | C/T | 4.94466e-05 | 0.00497201 | intron-variant | FBXW4 | GRCh38.p7 | 10:101624700 | TCAGCAAGCTTTCCC[C/T]CACCTCCTGGACTGG | 6468 |
rs763430299 | snp | C/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101676051 | GTGGTGGAGTTACAG[C/G]TTAGTTTTATTTTCT | 6468 |
rs763438771 | in-del | -/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101674589 | AGGAAAGGATGCTAA[-/T]GTACTGATTAGATAC | 6468 |
rs763443631 | snp | G/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101621736 | AACTGAAGCTCAGAG[G/T]GCCCCAGATCACAGC | 6468 |
rs763485940 | snp | C/T | 1.87682e-05 | 0.00306329 | intron-variant, synonymous-codon, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101694512 | GAGGGCCCGCATGTC[C/T]AGGTAGGAGCAGATG | 6468 |
rs763543234 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101610843 | CCCCAGCCCCGAGAG[A/G]TTGGTCAAGGGTGAG | 6468 |
rs763560747 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101666794 | AACAGTCAGGGCCAG[A/G]TGCAGTGGCTCATGC | 6468 |
rs763588718 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101658259 | AAAATAAAAAAAATG[A/G]TTTGAGGCCGGGCAT | 6468 |
rs763592228 | snp | G/T | 1.66991e-05 | 0.00288951 | utr-variant-3-prime, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101611290 | GGGGTGGCCCTGACG[G/T]TCATGGGTTTTGAAA | 6468 |
rs763601691 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101638091 | CTCCTCAATCCAGCA[C/T]GATCTTTCTAAGTGT | 6468 |
rs763607223 | snp | C/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101672387 | CCTTGGTGGATATCT[C/G]TGGACCGGGCAATTT | 6468 |
rs763607382 | snp | C/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101656961 | TTTTCAATTTGCATT[C/G]AAAACCATGAAAAGG | 6468 |
rs763700405 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101643746 | CTCCCTCTTCCCTCC[C/T]ACGGTAAGTGCTTTC | 6468 |
rs763777219 | snp | C/T | | | upstream-variant-2KB | FBXW4 | GRCh38.p7 | 10:101696079 | AAATTATACATGGGA[C/T]TTGCATTTGTGGCTC | 6468 |
rs763788238 | snp | C/G/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101686544 | GTCATGAATTAGGCA[C/G/T]TAGCAGACTAAGAGG | 6468 |
rs763789444 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101632219 | TATTCTCTACACACA[C/T]ACACACACACGCAAC | 6468 |
rs763823391 | snp | A/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101629257 | CATTATCCTATGTAA[A/T]CCTCATAACACTATG | 6468 |
rs763830333 | snp | A/G | 3.31978e-05 | 0.00407404 | intron-variant | FBXW4 | GRCh38.p7 | 10:101672894 | AGGGAGTAATAGTAT[A/G]TAAGGGGGAGACCAC | 6468 |
rs763833728 | snp | A/G | 3.29554e-05 | 0.00405914 | missense, intron-variant | FBXW4 | GRCh38.p7 | 10:101667964 | TGCCCCAGCCGGCCT[A/G]AGGCCAAAGGCCACA | 6468 |
rs763863824 | snp | A/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101694161 | GGAGGGTGCCTACTG[A/T]GGGATGCTCTCGGGA | 6468 |
rs763940753 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101630582 | TAAGTCCCAAAGCAT[A/G]AATACAGTGCGAAGG | 6468 |
rs763951750 | snp | A/C | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101682504 | TGTTTACAGTTATAT[A/C]TCTTCTCTTGAATTA | 6468 |
rs763951947 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101649404 | CACATAAACTCTGTT[C/T]CTCTCAGGCTTTTTA | 6468 |
rs763957239 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101644962 | GCTGTAGGAGCAGTT[C/T]GGCACATGGTTTGTA | 6468 |
rs763994294 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101683863 | CTCAGGAAAGGAAAG[C/T]GTCTCCAAGTGTACA | 6468 |
rs764039151 | snp | C/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101652669 | CAAGGAAAAGAAAAT[C/G]CTTATAAATCTCCAT | 6468 |
rs764085032 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101653849 | CACTCGGGGCCAGGC[A/G]CAGTGGCTCACGACT | 6468 |
rs764141285 | snp | C/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101638813 | TCGATGGCTTTCTGA[C/G]TGGTGAAAGCCTGGG | 6468 |
rs764153458 | snp | A/G | 3.31713e-05 | 0.00407242 | intron-variant | FBXW4 | GRCh38.p7 | 10:101611613 | TGCTGGAGAAGAGGT[A/G]GGCAGGACACTTACG | 6468 |
rs764172312 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101615078 | GTGTTCTTATAAAAA[C/T]GATTAGATTGCAATT | 6468 |
rs764208849 | snp | C/T | 1.64846e-05 | 0.0028709 | synonymous-codon, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101611688 | GTAGTAGGAGGAACC[C/T]GTGGCCAGCAGGTGG | 6468 |
rs764209641 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101616957 | AGCTCCTGGAAATCC[C/T]GTCTGGTAGCAGCTT | 6468 |
rs764213939 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101690632 | AAAGCAGTTCATCTT[A/G]CTCAACAAAGCTATG | 6468 |
rs764297313 | snp | G/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101616558 | CATTTCTGGCTGGGG[G/T]TGTTGACTGATTCTT | 6468 |
rs764337388 | snp | C/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101624175 | TCTATTTCCTGGTTT[C/G]ATTATTACATATTAT | 6468 |
rs764361435 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101646614 | CAGGGGACGCAGAGC[C/T]GGGAGGGGCAGCGGC | 6468 |
rs764377881 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101677739 | TACAGTGAGCAGTGA[C/T]TCCACCACTGCACTC | 6468 |
rs764397130 | in-del | -/CCT | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101663863 | CAACTCCAGGTGAGA[-/CCT]CCTCTACAGGAGAAG | 6468 |
rs764413511 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101671876 | CTTCCTGTGCTGGTG[C/T]GAGTACAAAGTAAGG | 6468 |
rs764437277 | in-del | -/A | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101635842 | AAGACCCGGTCTCAG[-/A]AAAAAAAAAAAAAAA | 6468 |
rs764531313 | snp | C/T | 3.2962e-05 | 0.00405954 | intron-variant | FBXW4 | GRCh38.p7 | 10:101624701 | CAGCAAGCTTTCCCT[C/T]ACCTCCTGGACTGGA | 6468 |
rs764562816 | snp | C/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101661772 | GGTCTTCTTTCCCTA[C/G]ACAAGACCCAGAAGA | 6468 |
rs764567673 | in-del | -/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101690761 | CCGGAGTGCAGGCCA[-/T]TAAGTCCACAGGTTC | 6468 |
rs764590220 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101634208 | AAATCTAACAAAAAA[A/G]ACAAGAGAAAAATGA | 6468 |
rs764591166 | in-del | -/TC | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101691615 | GATTCATTCCCAATA[-/TC]TCTCTTTTAGAGCAT | 6468 |
rs764592550 | in-del | -/TTTCTCTCCTGT | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101675492 | TCATAAAAATCCGTC[-/TTTCTCTCCTGT]TTTCTCTCCTGTAGT | 6468 |
rs764647625 | snp | A/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101658510 | AGATCGCGCCACTGC[A/T]CTCCAGCCTGGGCAA | 6468 |
rs764740242 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101618413 | AGGCACAGAGGGGGT[A/G]TTCTGGGCATGGGGT | 6468 |
rs764772574 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101693896 | GGCTTCTCTTAAGGT[C/T]CGAGCCCTGAAGCTT | 6468 |
rs764789245 | snp | C/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101685620 | ACAATACTGTTCAAA[C/G]AGTAACACACCAGAG | 6468 |
rs764831578 | snp | A/C | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101633124 | TAAGACAGAAATAGT[A/C]ATAGTACCTAGGCAT | 6468 |
rs764856271 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101669187 | GAAAAGAAAATAAAC[A/G]TACTAAGAGGATCCT | 6468 |
rs764859775 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101620066 | CCTCCAGTACTCCCC[A/G]CTCTCTGCCCAAGCC | 6468 |
rs764954386 | snp | A/C | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101662530 | AAGTCAAGTTTCTAC[A/C]CCTATACCACTCATA | 6468 |
rs765110393 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101627652 | GGGTACAACAGATAC[A/G]AGGAGCAGAGGAAGA | 6468 |
rs765121615 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101664960 | TTTAATATGACGAAA[C/T]TGAGGCTGGGAGCGG | 6468 |
rs765140285 | in-del | -/CGC | 0.000105613 | 0.00726605 | intron-variant, cds-indel, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101694447 | GGCGCCAGAGCAGAT[-/CGC]CGCAGCTGGTGAAGC | 6468 |
rs765144676 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101693887 | GGGACCGAGGGCTTC[C/T]CTTAAGGTCCGAGCC | 6468 |
rs765215709 | snp | A/C | 1.70536e-05 | 0.00292002 | intron-variant | FBXW4 | GRCh38.p7 | 10:101673071 | GAAATAAGGAGCCGA[A/C]CCCCAAGAACCAATT | 6468 |
rs765238970 | snp | G/T | 1.66255e-05 | 0.00288314 | intron-variant | FBXW4 | GRCh38.p7 | 10:101611598 | TCATGAGTCCTGGCA[G/T]GCTGGAGAAGAGGTG | 6468 |
rs765268934 | snp | A/G | 1.68021e-05 | 0.0028984 | missense, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101611397 | CTGAGGGGAGTCGAC[A/G]TCAGCGGGAAGGCCT | 6468 |
rs765304613 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101628707 | TCATAAGCACCACAA[C/T]CAGGTAAGAGATGAG | 6468 |
rs765396299 | snp | C/T | 1.64749e-05 | 0.00287005 | missense, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101673504 | CTCCTGCACTAACAA[C/T]ATGCGAGTTGGCCAG | 6468 |
rs765439061 | in-del | -/CCT | | | intron-variant, cds-indel, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101694604 | ACTCCCGAGCCGCCT[-/CCT]CCTCCTCCTCCTCCT | 6468 |
rs765485420 | snp | A/C | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101688979 | GGTCAACCCAGAGCT[A/C]AGGTTAAGTTGTCAC | 6468 |
rs765500045 | in-del | -/A | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101613394 | TGGGGGAAATGAAGG[-/A]AAAGGGGCGCCCTCC | 6468 |
rs765507652 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101667711 | GTTATCTCAATCCCA[C/T]GCATATATGAAGTGG | 6468 |
rs765543426 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101636692 | TCCCGGAATCAAGCA[A/G]TTCTTCTGCCCCAGC | 6468 |
rs765575353 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101687609 | TTAATCTACCAATCT[C/T]CAAGTTAGGGTTCCT | 6468 |
rs765667895 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101671041 | GCAAATTCTTATGAA[A/G]GTTCAGGTGTATTAG | 6468 |
rs765670207 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101675832 | TATACTTGCTCTAAG[C/T]TCTAACTCCTGTAAC | 6468 |
rs765670779 | in-del | -/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101638271 | ACTAGAATGCTGCAG[-/T]CAAAAAGAACATGGT | 6468 |
rs765690760 | snp | C/T | 4.99114e-05 | 0.00499532 | synonymous-codon, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101612396 | GCCACAGGACAGCAG[C/T]GTGAAAGGGGACTCA | 6468 |
rs765745732 | snp | G/T | 3.56837e-05 | 0.00422381 | intron-variant | FBXW4 | GRCh38.p7 | 10:101612518 | GGCTGCTCCACGTGG[G/T]TCATACACATTCGTT | 6468 |
rs765758015 | snp | A/C | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101674450 | GATTCCCATACATAC[A/C]TCTTCCGCAATAGAT | 6468 |
rs765767100 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101629772 | AAGAGTTAGTCTTGT[C/T]TGAATCTCCAGCATC | 6468 |
rs765792909 | snp | A/G | 1.65373e-05 | 0.00287548 | stop-gained, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101676411 | GAGACACCTTCACTC[A/G]TTCCTTCACTGGGAC | 6468 |
rs765803908 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101691589 | TGTTGTTATTATTGC[C/T]ACAGAATGTAGATTC | 6468 |
rs765845910 | snp | C/T | 0.000284051 | 0.0119141 | intron-variant, synonymous-codon, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101694395 | CAGGTCGGTGCCGAG[C/T]CGCGTGAAGCCGGAG | 6468 |
rs765859487 | snp | C/T | 1.64876e-05 | 0.00287116 | intron-variant | FBXW4 | GRCh38.p7 | 10:101667841 | CTAGTAAAATAAAAG[C/T]ATTATTATACAGGAC | 6468 |
rs765859592 | snp | A/C | 2.99585e-05 | 0.00387019 | intron-variant, utr-variant-5-prime, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101694654 | ATGGCCACCCCTGTC[A/C]CCGCGATGTCGGCCC | 6468 |
rs765861153 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101632196 | TCTCCCAGTACACAT[A/G]CCACACATATTCTCT | 6468 |
rs765910605 | snp | A/C | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101669077 | AGTCACATGATAACT[A/C]TTCCCTATAAAAGGA | 6468 |
rs765974904 | in-del | -/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101680627 | TGTACATTAAAACAA[-/T]TTTTTAAAGTACACC | 6468 |
rs766018933 | in-del | -/AAT | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101681718 | GAGACTCCGTCTCAA[-/AAT]AATAATAATAATAAT | 6468 |
rs766021845 | snp | G/T | 2.2659e-05 | 0.00336586 | intron-variant, missense, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101694547 | GCAGCAGCTCCTCCG[G/T]CAGGCGCCAGAGCGC | 6468 |
rs766034650 | in-del | -/CTCA | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101621976 | TAAAGGGTGGGCATT[-/CTCA]CTCACAGAGCTACCA | 6468 |
rs766068960 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101616899 | AAAAGTGACAATGTC[A/G]TATAGCAAGGAAAGG | 6468 |
rs766072549 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101693290 | CTGATTTTTAAAAAA[C/T]ATGTATGGTAATGAC | 6468 |
rs766091939 | snp | G/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101618122 | CTCCAGACAGAAGGG[G/T]CTCCAGCCAAATGTC | 6468 |
rs766116373 | in-del | -/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101688457 | GGGCAATGTGGACAG[-/T]TTGGATAAAATGAAG | 6468 |
rs766146955 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101654169 | TATCCTTTTAAAAAA[C/T]TCTAGTATGTTTACT | 6468 |
rs766203565 | in-del | -/CC | 3.41082e-05 | 0.00412952 | intron-variant | FBXW4 | GRCh38.p7 | 10:101673071 | GAAATAAGGAGCCGA[-/CC]CCCAAGAACCAATTA | 6468 |
rs766213959 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101670616 | TCTCTTCTCATCCTA[A/G]GGATAAGAGGCTTTA | 6468 |
rs766256417 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101622104 | TCATTGATTAAAACA[C/T]CTCATGTTGTTTTAA | 6468 |
rs766293320 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101655362 | CGGACCAAAGACTTC[C/T]AACAACTGGAAGAAT | 6468 |
rs766302639 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101612607 | ACTCAAGGAAGGGGG[C/T]TCAGGGAGGAGATGC | 6468 |
rs766310340 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101676958 | AACATCTGCTCACCA[A/G]AATGAATACACAAGC | 6468 |
rs766323576 | snp | C/T | 1.66713e-05 | 0.0028871 | intron-variant | FBXW4 | GRCh38.p7 | 10:101611577 | TCTCCCAAATGCAGC[C/T]CATAATCATGAGTCC | 6468 |
rs766400946 | snp | A/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101627510 | CTACTCCCCACTACC[A/T]GCAGCCATTCTTGCC | 6468 |
rs766416719 | snp | A/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101664940 | TAAAGGAAATAGTAT[A/T]CATATTTAATATGAC | 6468 |
rs766424276 | snp | A/C | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101628487 | TAGCACAGTGCCTGG[A/C]CCAGAGAAGGCACTC | 6468 |
rs766503327 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101663920 | TTAAAAACAGGATTA[C/T]CGGTGTTGAACAATA | 6468 |
rs766505338 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101679097 | CTGTAGATAAGTATA[C/T]ATGCATGTTGCCCAG | 6468 |
rs766528179 | snp | A/G | 4.99896e-05 | 0.00499923 | missense, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101612386 | AGGTGTCATAGCCAC[A/G]GGACAGCAGTGTGAA | 6468 |
rs766609007 | snp | C/G | 1.64798e-05 | 0.00287047 | missense, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101672937 | GTCCTGTCCCTGGAG[C/G]CACTCACAATGATGC | 6468 |
rs766640333 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101636326 | TTGAGCCACTGCACT[C/T]CAGCCTGGGTGAGAG | 6468 |
rs766682177 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101613509 | CACAGGGATGTCCAG[A/G]TAAGAGGCCCTGGCA | 6468 |
rs766720364 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101687444 | AACAGCGTACCCTAA[C/T]CCAAAATACTTGCTT | 6468 |
rs766772022 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101634913 | TAACAAAAACTTCTA[C/T]ACAACAGAAGACATC | 6468 |
rs766772671 | in-del | -/AAG | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101655334 | CCTTATCAGCCTGCA[-/AAG]AAGGATTTTCCGGAC | 6468 |
rs766802705 | snp | C/T | 1.83189e-05 | 0.0030264 | intron-variant | FBXW4 | GRCh38.p7 | 10:101611817 | TAGGGTACCCTCCAC[C/T]TCTACCCCAGCTTTC | 6468 |
rs766850913 | snp | G/T | 4.95798e-05 | 0.0049787 | missense, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101676395 | CCCAGTCTCCAGTTC[G/T]GAGACACCTTCACTC | 6468 |
rs766902317 | snp | A/C | 4.87983e-05 | 0.00493931 | intron-variant | FBXW4 | GRCh38.p7 | 10:101694340 | TCCCGGGACGCGGGG[A/C]CGGCTCGGGGCGGGG | 6468 |
rs766984798 | snp | A/G | 1.8745e-05 | 0.0030614 | intron-variant, synonymous-codon, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101694515 | GGCCCGCATGTCCAG[A/G]TAGGAGCAGATGAGC | 6468 |
rs766994168 | snp | A/C | 1.78159e-05 | 0.00298457 | intron-variant | FBXW4 | GRCh38.p7 | 10:101673693 | AATGATGGAAAAGAA[A/C]ATTTAAAAGTCATCA | 6468 |
rs766995517 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101635036 | CAGGACGCACAGTAG[A/G]AGGTAAGTGGTGGGC | 6468 |
rs767014232 | snp | G/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101645270 | CAGCCTCTTCTTTTT[G/T]GGGGGAAGCCCAGTC | 6468 |
rs767028517 | snp | C/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101659602 | TGCTGATGGGAAGGA[C/G]ACCAGAGCAGGGATG | 6468 |
rs767034899 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101622342 | TTCTTAGACTTGACA[C/T]CAAAGGCACAGTCAA | 6468 |
rs767049873 | snp | A/C | 1.74695e-05 | 0.00295541 | intron-variant, missense, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101694405 | CCGAGCCGCGTGAAG[A/C]CGGAGTTGAGCGAGG | 6468 |
rs767114753 | snp | A/C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101681194 | GGAGTTTGAGACCAG[A/C/T]CTGGCCAACATGGTG | 6468 |
rs767221791 | in-del | -/AC | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101622289 | AATGTGGCATTTAAG[-/AC]ACAGACCACATGTGG | 6468 |
rs767227069 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101649754 | TTGGTGAACCTTGGC[A/G]GGATGCCTCCCCAGG | 6468 |
rs767304438 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101615027 | AGCTGTCTGTCTCCT[C/T]ATCCCCTCCTCCTGG | 6468 |
rs767306986 | snp | A/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101634227 | AGAGAAAAATGAACA[A/T]ATAAACAAAAATCAC | 6468 |
rs767309881 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101655192 | TTGTCTGGTTATTGC[C/T]TTACAATGAATTCCT | 6468 |
rs767313788 | snp | A/C | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101653946 | GCCAACATGGTCAAA[A/C]CCCATCTCTACTAAA | 6468 |
rs767332950 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101631986 | CCATGACTCAGGGCC[A/G]AGGGCAGGCAGACCT | 6468 |
rs767335263 | in-del | -/CA | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101612825 | TCACATGCACATGCA[-/CA]CACACACACACACAC | 6468 |
rs767390557 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101669011 | TTAAAGGAAACATTC[C/T]TTGAGTTTAAAGGGT | 6468 |
rs767417362 | snp | C/G | 3.29859e-05 | 0.00406102 | missense, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101672920 | ACCACCTCACCTTGG[C/G]CGTCCTGTCCCTGGA | 6468 |
rs767424144 | snp | G/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101620670 | TTGATAAGAAACAAG[G/T]TCTCACCATATTGCC | 6468 |
rs767472289 | snp | A/G | 3.32757e-05 | 0.00407881 | intron-variant | FBXW4 | GRCh38.p7 | 10:101673051 | ATCTTCCCATCCCTA[A/G]GAGAGAAATAAGGAG | 6468 |
rs767476804 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101684210 | CTCACTGCAACCTCC[A/G]CCTCCCAGGTTCACG | 6468 |
rs767478755 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101667821 | GATTTTCTAGCTCAC[C/T]TGATCTAGTAAAATA | 6468 |
rs767503924 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101640074 | CCTCTACTGGACACC[C/T]TGGGGCCTAAGAAGA | 6468 |
rs767521128 | snp | A/G | 1.69861e-05 | 0.00291424 | intron-variant | FBXW4 | GRCh38.p7 | 10:101611780 | ATTTCCTGTCCAGGA[A/G]GAGGAGAAGCAGAGG | 6468 |
rs767531361 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101650527 | TTTAACTCACTTCAA[A/G]CTGGCAGCCCTATGG | 6468 |
rs767550994 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101676872 | CTAAGAAGGTAGACA[C/T]AGATTTCTTAGGACA | 6468 |
rs767574286 | snp | A/C | | | intron-variant, missense | FBXW4 | GRCh38.p7 | 10:101625660 | AGTGCTGGCCTAGAA[A/C]TTGAACCTATGAGCC | 6468 |
rs767641841 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101691985 | TATTTGCAATAAAAA[C/T]GAAATGCATAACATT | 6468 |
rs767645171 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101680109 | AAATACTGATTAAAA[C/T]AGTAATAATAAATGC | 6468 |
rs767728466 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101663674 | CCTTCTGTGTTACTC[C/T]TGGGAAGTTGCTCAG | 6468 |
rs767749976 | snp | A/G | 1.64852e-05 | 0.00287094 | missense, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101611695 | GAGGAACCTGTGGCC[A/G]GCAGGTGGTTGCCAT | 6468 |
rs767788302 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101664727 | ACACCAGGCAAGAAA[A/G]GATTCTGGTTGACAT | 6468 |
rs767940274 | in-del | -/GAGTC | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101655710 | GGAAACACCCTGCAT[-/GAGTC]GAGTCCTTGGGAGAA | 6468 |
rs767959018 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101663431 | CATTTCCTCATACTT[C/T]AGTATTTACTGTATT | 6468 |
rs767966331 | snp | G/T | 1.71261e-05 | 0.00292622 | intron-variant | FBXW4 | GRCh38.p7 | 10:101673681 | GCATCTGACTGAAAT[G/T]ATGGAAAAGAAAATT | 6468 |
rs767971103 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101670974 | CTTTCCTAAAATACA[A/G]TACATATTTGGGAAA | 6468 |
rs767977679 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101633185 | TAAATTAGTTCAACC[A/G]TTGTGGAAGACAGTG | 6468 |
rs767992268 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101649218 | TCTAATTTGTTTCTA[C/T]GATTTCATCTCTCTC | 6468 |
rs767996297 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101648054 | CACCCAATCATCAGG[A/G]AGGTCCCTGTCCACT | 6468 |
rs768180878 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101689655 | CACAGTTTAGGCCTT[A/G]AATGTAACCAGTTAG | 6468 |
rs768227529 | in-del | -/GCC | | | intron-variant, cds-indel, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101694596 | GCAGCCGACTCCCGA[-/GCC]GCCGCCTCCTCCTCC | 6468 |
rs768249358 | snp | G/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101675271 | TGTGGCACACTCAAG[G/T]AGGCAGCAAACAGAG | 6468 |
rs768272459 | snp | A/G | 3.31214e-05 | 0.00406935 | intron-variant | FBXW4 | GRCh38.p7 | 10:101673450 | GTCCCCGAAGTATAA[A/G]ATGGAAAAGGGTGGA | 6468 |
rs768317150 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101636226 | GCTGGGGGTGGTGGC[A/G]TGCACCACCTAACTA | 6468 |
rs768317235 | snp | A/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101653228 | CCCACTGTCCCTACG[A/T]GTCTGGTCCCTTCCT | 6468 |
rs768357561 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101670423 | ATCTAGCACAGCAGC[A/G]AAGTATTTGGCAGGT | 6468 |
rs768402822 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101624885 | GCTAACAATGGGAAA[C/T]GCCGTGCTCATTCCC | 6468 |
rs768447244 | snp | A/C | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101660939 | TGTCTCTCTAGTGAC[A/C]AGAACATGGTAATGC | 6468 |
rs768464022 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101637071 | ATTTTGAAAATTTCC[A/G]TTATAAAAACATTTT | 6468 |
rs768593857 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101652612 | GAACTAGAAAAAAAA[A/G]GCAAATTTATTATAG | 6468 |
rs768594090 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101656457 | TTAAGAGAGAACACA[C/T]AAATGAGCCTTGGCT | 6468 |
rs768601295 | snp | C/T | 1.66369e-05 | 0.00288412 | intron-variant | FBXW4 | GRCh38.p7 | 10:101676466 | AACAGATAATCCAAT[C/T]ACTACAACTTATTGC | 6468 |
rs768613666 | snp | G/T | 3.32834e-05 | 0.00407929 | missense, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101611759 | GCTCCTCCCACTCCA[G/T]GACACATTTCCTGTC | 6468 |
rs768700162 | in-del | -/TGAA | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101629833 | CAAATGCTTATTGAT[-/TGAA]TGAATGAATGAATGG | 6468 |
rs768727635 | snp | G/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101690098 | ATAAGACTGGCAATA[G/T]AATCTTTTAAAAATA | 6468 |
rs768762737 | snp | A/T | 1.65419e-05 | 0.00287588 | missense, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101676345 | AGGCTACTTGCCTGC[A/T]TCTCCACTTCAGCAG | 6468 |
rs768795128 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101617914 | AGAATGAAAAAAAGC[C/T]ATCAGTAATGCTTTC | 6468 |
rs768806186 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101632834 | CCTGAGAAATGATGA[C/T]ACAATATTCACAAAA | 6468 |
rs768810975 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101656083 | CCACACAAAGGAAGC[A/G]AAGAAGCCCCCACAG | 6468 |
rs768870430 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101685113 | ACTGCCAGCCCCAGC[C/T]TACCTTTGCCCCTGA | 6468 |
rs768893492 | in-del | -/AGG | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101619805 | CCAGCCCAGCCTGCA[-/AGG]AGAACAGTCTCTAGT | 6468 |
rs768955049 | snp | A/C | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101626742 | ATCCGCCCACCTTGG[A/C]CTCCGAAAGTGCTGG | 6468 |
rs768962263 | snp | A/G | 4.94214e-05 | 0.00497074 | missense, intron-variant | FBXW4 | GRCh38.p7 | 10:101667937 | TCTTCAGTCTGGATG[A/G]TGTGTAAGCACTGCC | 6468 |
rs769000141 | snp | A/C | 1.65512e-05 | 0.00287669 | intron-variant | FBXW4 | GRCh38.p7 | 10:101624854 | ATCTGGCTTGTCAGA[A/C]CCTGTGGTGGAAATG | 6468 |
rs769002818 | in-del | -/TTTAGGGTACCCTCCACCTCTACCCCAGCTTTCTTGGGCCTA | 1.74208e-05 | 0.00295129 | intron-variant | FBXW4 | GRCh38.p7 | 10:101612485 | CTGCCCACTGGGAAG[lengthTooLong]GGAAGGACGGAGTGA | 6468 |
rs769043866 | in-del | -/TT/TTT | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101640489 | TTTCTTTCTCTTTTT[-/TT/TTT]TTTTTTTTTTTTTTT | 6468 |
rs769059563 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101678848 | TAGAAAGAATGGTTT[C/T]GGCAGGCAGAAAGAA | 6468 |
rs769100895 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101682452 | CCCTGTCTGCTCCTC[A/G]TATCTGCAAATCCCT | 6468 |
rs769214158 | in-del | -/AAG | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101687015 | CAGGGAAAAAAGGAA[-/AAG]AAGTACTCAAAGACT | 6468 |
rs769220826 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101628249 | GAAAGAAAATTCAAA[C/T]GGCTTTTGCCCTCAG | 6468 |
rs769235550 | snp | A/G | 5.83448e-05 | 0.00540083 | intron-variant, utr-variant-5-prime, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101694642 | GCCGCCGCCGCCATG[A/G]CCACCCCTGTCCCCG | 6468 |
rs769259928 | snp | G/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101611908 | GCCTAAATCATCAGA[G/T]TCATCAAAAACCGAA | 6468 |
rs769265501 | snp | A/C | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101686872 | AAGGGATGAAGTTCT[A/C]CCTTAGCAACTCACT | 6468 |
rs769301181 | snp | A/G | 1.76852e-05 | 0.0029736 | missense, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101612338 | CCCAGCACACTCACC[A/G]GACGCTGGTGCGGAG | 6468 |
rs769305940 | in-del | -/AA/AAA | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101681388 | GCGAAACTCCGTCTC[-/AA/AAA]AAAAAAAAAAAATAA | 6468 |
rs769341173 | snp | C/T | 3.34353e-05 | 0.00408859 | intron-variant | FBXW4 | GRCh38.p7 | 10:101672865 | GATCTATCCACCCCC[C/T]CCCTATAGACAGGAG | 6468 |
rs769369320 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101651059 | TGCAAGCATTGTGTG[A/G]GGACCATTAATGCAT | 6468 |
rs769386031 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101672209 | CAGCAAAGTTCCCAC[A/G]GCAACCCTAAAGGAC | 6468 |
rs769390052 | snp | C/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101688430 | CCATTGGGTGGCCCA[C/G]ACTTCCAGGGAGGGC | 6468 |
rs769411936 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101623202 | CTAGGCAGACAGATC[A/G]CTTGAGCCCAGGACT | 6468 |
rs769457129 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101649056 | CATAAATACAATTAT[A/G]TTTTTAAAGGAAAAA | 6468 |
rs769459293 | snp | A/C | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101665741 | AGACTCTGTCCTCAA[A/C]CTCTTTTATTGACAC | 6468 |
rs769460507 | snp | C/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101621561 | TCCACAAACTCCGAG[C/G]TACTAGTTTGGGTGG | 6468 |
rs769552458 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101635923 | CCCTACCCTGGGGGG[A/G]CGGGCGGAGGGAAGA | 6468 |
rs769574767 | snp | A/C/T | 3.33785e-05 | 0.00408514 | intron-variant | FBXW4 | GRCh38.p7 | 10:101676296 | TTACTTTCCATTATG[A/C/T]TTTTATGTCCCAAGT | 6468 |
rs769579400 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101673885 | TGATCTAAACTTCCC[C/T]GGACTTTGTAAAAGA | 6468 |
rs769699293 | in-del | -/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101632122 | CCAGATCAGAAGGGA[-/G]GTGCCCCACTGGCCT | 6468 |
rs769720708 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101686048 | CCCACATGTCAAAAA[C/T]GTCTAAACAGTTTCA | 6468 |
rs769727408 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101689831 | CATCACTGAAATAGA[C/T]ACCCCAGGCCCCCAG | 6468 |
rs769857019 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101667338 | AGTAAAGCCATCATC[A/G]AAATTTCACACTTTT | 6468 |
rs769933630 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101682434 | GAAAAAAAAAATAGA[C/T]TTCCCTGTCTGCTCC | 6468 |
rs769935720 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101645892 | CTCCAACACTGGCTG[C/T]GTTGGCTATGAGAGA | 6468 |
rs769937106 | snp | A/G | 1.64738e-05 | 0.00286995 | stop-gained, intron-variant | FBXW4 | GRCh38.p7 | 10:101667920 | CAATGGACCAGACTC[A/G]GTCTTCAGTCTGGAT | 6468 |
rs770014511 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101630405 | TGGCACCTGGGGGCC[C/T]CCCGATTTCCCTTGG | 6468 |
rs770047650 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101668664 | TGCTTGGAGCACATT[A/G]TCTGGTCTCTATCAG | 6468 |
rs770085668 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101656018 | TTCACTTTACCTCAC[A/G]CATCTCAGCTTTTTC | 6468 |
rs770105716 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101617767 | TGAAACGCAAAGTAT[C/T]AGTTTGGTGTCAGCA | 6468 |
rs770134007 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101639524 | AGTAGACACCTATTG[C/T]TCTGTGTGCCCACAT | 6468 |
rs770163435 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101620060 | ACTGCCCCTCCAGTA[C/T]TCCCCGCTCTCTGCC | 6468 |
rs770171079 | snp | A/G | 1.64789e-05 | 0.0028704 | missense, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101624799 | CAACAAGCCGTCCCT[A/G]TCACAAAAGAGCTGC | 6468 |
rs770171502 | snp | C/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101654873 | CTGTCACCAAGGCTA[C/G]AGTGCAGTGGCACGA | 6468 |
rs770211902 | snp | C/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101616333 | AGTCGAGCATCTTCT[C/G]TATACAAAGCATTGT | 6468 |
rs770256684 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101691480 | CCCTAGGACATGGGC[A/G]AGAAATCAAAACACA | 6468 |
rs770271071 | snp | A/G | 0.000561246 | 0.0167424 | intron-variant, synonymous-codon, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101694497 | CTGGGCCAGGCGGCC[A/G]AGGGCCCGCATGTCC | 6468 |
rs770305226 | snp | C/T | 1.6476e-05 | 0.00287014 | intron-variant | FBXW4 | GRCh38.p7 | 10:101611444 | GAAGTGGTAAGAGCT[C/T]TCCAAGTGGGACATG | 6468 |
rs770336653 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101690449 | TGACTGACTCCAACT[A/G]TCTTTGTGTCCCTTT | 6468 |
rs770349219 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101641560 | ATCCCTCTGAGTGAC[A/G]TGTGCACACAAACAC | 6468 |
rs770366648 | snp | A/C | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101629674 | CAACTAGTGGACTGG[A/C]ATTGGAACCCAGTCA | 6468 |
rs770381711 | snp | G/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101677940 | ATGCACACTGAAGCC[G/T]TTAGGGATAAATGTA | 6468 |
rs770397279 | snp | G/T | | | intron-variant, downstream-variant-500B | FBXW4 | GRCh38.p7 | 10:101625283 | GGTTTTAAGAGCTGG[G/T]GGAATCTGGTAATGT | 6468 |
rs770450679 | snp | G/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101641177 | GGCATTTAAGAGATA[G/T]ATAATTTAAATATAT | 6468 |
rs770456923 | snp | A/C | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101664229 | CAAGTGCCTGAGTAC[A/C]TACATAAGAAGATAA | 6468 |
rs770483782 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101674519 | AGGGAAGCCCCATTC[C/T]CTTATTCTGTTAGAG | 6468 |
rs770518721 | snp | C/T | 0.000116056 | 0.00761674 | missense, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101611747 | TGCTGTCGTGGGGCT[C/T]CTCCCACTCCATGAC | 6468 |
rs770521797 | snp | A/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101647315 | AGAGTGCTGACCCTG[A/T]ACCTTCCTTGGGTGA | 6468 |
rs770573355 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101685509 | AAATATTGCCCATGA[C/T]ACAATTTGCTGAAAA | 6468 |
rs770623829 | snp | C/T | 3.29614e-05 | 0.00405951 | intron-variant | FBXW4 | GRCh38.p7 | 10:101673485 | GAAACCTATAGCACT[C/T]ACCCTCCTGCACTAA | 6468 |
rs770623845 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101671882 | GTGCTGGTGTGAGTA[C/T]AAAGTAAGGCAGAAA | 6468 |
rs770624485 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101613150 | GCCTGCTCCCCCCAC[C/T]CTCACCCCACCCGGG | 6468 |
rs770650338 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101650874 | AGGGGGAGCACACAT[C/T]GGATACAAAGATCGG | 6468 |
rs770656179 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101619890 | CAGGTTCTGTGAGAA[A/G]CAGCATTGGCTGTCT | 6468 |
rs770656903 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101648813 | AAAGTCAGGTTTTCT[A/G]ATCAGTATTGTTCCT | 6468 |
rs770733611 | snp | A/C | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101634006 | TAATCTCAGCTACTC[A/C]GGAGGCTGAGGCAGG | 6468 |
rs770779462 | in-del | -/GTG | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101639591 | TGTTCTTACATGACT[-/GTG]TTCCCTCCCTGGCCA | 6468 |
rs770806032 | snp | C/T | 0.000181191 | 0.00951644 | missense, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101673596 | CTGGCACCATCTGGA[C/T]GGAACTGGTAGGCCA | 6468 |
rs770906762 | in-del | -/C | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101651602 | AATGGCCCTTCTCTG[-/C]CCCCCTCCTTCCCTC | 6468 |
rs770924022 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101621319 | ATCACTTGAGCCAAC[A/G]AGTTCGAGACCAGCC | 6468 |
rs770947117 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101673452 | CCCCGAAGTATAAGA[C/T]GGAAAAGGGTGGAAG | 6468 |
rs771028699 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101614574 | GCCCTGGAGGCCAGC[A/G]CAAGTCCTGAGAGCC | 6468 |
rs771078614 | snp | A/G | | | intron-variant, missense, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101694600 | GCCGACTCCCGAGCC[A/G]CCTCCTCCTCCTCCT | 6468 |
rs771096575 | snp | A/G | | | upstream-variant-2KB | FBXW4 | GRCh38.p7 | 10:101695565 | AGGTTCCATAGCTTA[A/G]GTTCTCACACAGGCC | 6468 |
rs771161681 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101631467 | AAAAAAAAGAGCCTA[C/T]GCAGAGAAAAGGAAA | 6468 |
rs771164226 | snp | G/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101659040 | CCCAAGCCGAAGCAG[G/T]CTATAGAGATCAGTT | 6468 |
rs771164514 | snp | A/C | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101643352 | GGTGCTGGGATTTGG[A/C]CCCTGGGAAGAGAGA | 6468 |
rs771226213 | snp | A/C | 1.65611e-05 | 0.00287755 | missense, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101611367 | GTGGTGAGACGCAGG[A/C]AGTACACAGGGCTGC | 6468 |
rs771269021 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101668485 | GAATGGAAGAAGAAG[A/G]GAGACTTCCAAGTGG | 6468 |
rs771280307 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101616049 | TGTTCTCTGGAGACC[C/T]TATGCTCCAGAGACC | 6468 |
rs771306543 | snp | A/C | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101670763 | CAGGCTCATTAAGAA[A/C]ATAAGCTACCAGCTG | 6468 |
rs771315422 | snp | C/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101653341 | TTTAACTGCTTCAAT[C/G]TGGCCCAAAACGGTC | 6468 |
rs771457386 | snp | C/T | 4.94425e-05 | 0.0049718 | synonymous-codon, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101672993 | CTCCTGTTCATGAGC[C/T]GAGTACTTGACAGTG | 6468 |
rs771482161 | snp | C/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101661012 | GGTATTGAGGAGGAA[C/G]GGAGAGAGAAAGAAA | 6468 |
rs771498699 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101675559 | ATTATTCACAGTATC[C/T]GATGCCAGTGAAACC | 6468 |
rs771502918 | snp | C/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101639389 | AAAGGCTGTACAACA[C/G]TTCCTATCAGACTCT | 6468 |
rs771511218 | snp | A/C | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101638036 | TACGGTCTAACTGGA[A/C]GGCAATGTGGTGGTG | 6468 |
rs771521057 | in-del | -/A | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101667230 | GCGAGACTCCGTCTC[-/A]AAAAAAAAAAAAAAA | 6468 |
rs771609733 | snp | C/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101677251 | TTCAGTCATAATAGC[C/G]AAAAGTGGTAAACAG | 6468 |
rs771654851 | snp | C/T | 6.58892e-05 | 0.00573936 | missense, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101673572 | ACTCCCAGAGGCCGA[C/T]GATTCAAGCTGGCAC | 6468 |
rs771682989 | snp | C/T | 1.64857e-05 | 0.00287099 | stop-gained, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101611655 | CCTTTGACGCCGGTC[C/T]CACAGCCGTACAACA | 6468 |
rs771718599 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101691361 | CTCTCCACCTGCTGT[A/G]ACACGCATAACTTCT | 6468 |
rs771730611 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101623864 | TCCATTTATGTAACA[C/T]TTGCAAAATGACAAA | 6468 |
rs771731504 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101685307 | AATTTAGTCATAAAT[C/T]CCACAGGATCAAGTC | 6468 |
rs771796650 | snp | G/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101632981 | AATACCAGGGTCAGA[G/T]GAGGTAGCTGGCATG | 6468 |
rs771808057 | snp | A/C | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101662628 | CCACACTCTCTCACA[A/C]GATAGCAAGTGTCCT | 6468 |
rs771908241 | snp | C/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101626407 | GCTGGAAACATAATA[C/G]CCACTTGGAAATCAT | 6468 |
rs771930157 | snp | A/G | 1.74263e-05 | 0.00295175 | intron-variant | FBXW4 | GRCh38.p7 | 10:101612486 | CTGCCCACTGGGAAG[A/G]GAAGGACGGAGTGAG | 6468 |
rs771960602 | snp | C/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101618274 | GCTGACCAGGTGGCC[C/G]TTATCAGTGTTCCAA | 6468 |
rs771963669 | snp | A/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101693029 | GTAATAAATGGGCAA[A/T]GAGTGGGAAGAGACA | 6468 |
rs771993990 | snp | A/C | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101686173 | GGTTCTGTATTTGCA[A/C]GGCACTTGACCAGTA | 6468 |
rs772070739 | snp | A/G | | | intron-variant, downstream-variant-500B | FBXW4 | GRCh38.p7 | 10:101625509 | GAGGCACACGAGAAG[A/G]AGCAGGCTGACCCTG | 6468 |
rs772072053 | snp | A/G/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101661608 | TCCGGGTGTCATGAC[A/G/T]CCCCTTCTAGCCATG | 6468 |
rs772086554 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101670462 | AACAATAATGGTGAT[C/T]CTTATTACAATAAAT | 6468 |
rs772089125 | snp | A/G | 0.000108196 | 0.00735433 | intron-variant, missense, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101694436 | CCCGGGCTATCCGGC[A/G]CCAGAGCAGATCGCA | 6468 |
rs772128782 | snp | A/G | 3.33606e-05 | 0.00408401 | intron-variant | FBXW4 | GRCh38.p7 | 10:101676480 | TCACTACAACTTATT[A/G]CCAACCACAGAAAAT | 6468 |
rs772135623 | in-del | -/C | 1.64912e-05 | 0.00287147 | intron-variant | FBXW4 | GRCh38.p7 | 10:101624819 | AAAAGAGCTGCCAAA[-/C]AAAAGGAGAACAAAG | 6468 |
rs772144782 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101679033 | AAAGTGAGTCTTTCT[C/T]GAAACCCCTAGCCAA | 6468 |
rs772198484 | in-del | -/A | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101657684 | CTATCTGAAACTTCT[-/A]AAGAGTCTTGTTCAA | 6468 |
rs772209511 | in-del | -/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101618887 | TCTCAAATGCCCCTT[-/G]GGCAGAAAAAAAAAA | 6468 |
rs772224076 | snp | G/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101643069 | GAGAAGGCAGGGCTT[G/T]GCCAACAGGAGACTC | 6468 |
rs772286484 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101671327 | TCACTGACCTAAAAG[A/G]AATCCTCAGAAGGAA | 6468 |
rs772352684 | snp | A/G | 1.65299e-05 | 0.00287483 | intron-variant | FBXW4 | GRCh38.p7 | 10:101668023 | TTGGCATTGCCTGGG[A/G]TCAGTGGGGAGGAGA | 6468 |
rs772376608 | snp | C/G | 1.697e-05 | 0.00291285 | utr-variant-3-prime, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101611272 | TTCCCTGGCCCAGAG[C/G]CAGGGGTGGCCCTGA | 6468 |
rs772380433 | snp | A/C | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101630242 | CTGAGCCTTATTACT[A/C]TCTATTACTCCAATT | 6468 |
rs772384082 | in-del | -/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101679398 | TTATATTTCTAGAAA[-/G]TATATTCTTTTCAAT | 6468 |
rs772414999 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101629924 | GCAGGGCAGCACAAG[C/T]GGCGTGCTCAGCAGC | 6468 |
rs772463678 | in-del | -/CAGA | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101645822 | CACAGGACAGGCAAG[-/CAGA]CAGAGTAGCACGGAA | 6468 |
rs772482029 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101665816 | AACACATTCCAGAGG[A/G]GGAGGCTGGAATAGA | 6468 |
rs772498170 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101680053 | CATCCAAGTTGCACA[A/G]AAGTCATTATTTCAT | 6468 |
rs772510393 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101644369 | ATTGTCATCCTCCCA[A/G]TCTGCATCTTCCAAA | 6468 |
rs772525751 | snp | A/G/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101648131 | AAGAAGATATCCTGC[A/G/T]ATTTGGGTTTTTTTG | 6468 |
rs772591522 | snp | A/C | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101642976 | TGCACAGGTCAACTT[A/C]CCTCCCTGCCATCCT | 6468 |
rs772602863 | snp | C/T | 3.29511e-05 | 0.00405887 | missense, intron-variant | FBXW4 | GRCh38.p7 | 10:101667949 | ATGGTGTGTAAGCAC[C/T]GCCCCAGCCGGCCTG | 6468 |
rs772633641 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101614475 | GGAAAATGTCATGGC[C/T]GTAAGTATCTGCAGT | 6468 |
rs772642057 | snp | A/C | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101674440 | AAGGTTCTAGGATTC[A/C]CATACATACCTCTTC | 6468 |
rs772764964 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101662733 | ACGAGGAGCTGTGGG[C/T]GCCTCTCCCTTCCCC | 6468 |
rs772786841 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101647559 | ATGTTTTTGTCTTGC[A/G]TTTCTGAAATCCCAA | 6468 |
rs772823052 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101661086 | TGAGGGATAGAAATG[C/T]ATCCCTGTTAGCAGG | 6468 |
rs772837107 | snp | G/T | | | downstream-variant-500B | FBXW4 | GRCh38.p7 | 10:101610396 | TGTGTTGGGGTAGGG[G/T]TCACCACAGGCAACA | 6468 |
rs772874688 | snp | A/C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101646453 | GGCTAGGCAGGAGGC[A/C/T]GAGAGGCACAGGTGG | 6468 |
rs772959678 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101633771 | TATATCAGCAATAAC[A/G]AACTGTTATTATATA | 6468 |
rs773036998 | snp | C/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101618320 | AAAGGGCCACCAACT[C/G]CAGCCACAGGGGTCA | 6468 |
rs773049562 | snp | A/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101633002 | AGCTGGCATGTTGCA[A/T]ACAACAGTAGAAAGG | 6468 |
rs773113504 | snp | C/G | 1.67343e-05 | 0.00289255 | intron-variant | FBXW4 | GRCh38.p7 | 10:101673054 | TTCCCATCCCTAGGA[C/G]AGAAATAAGGAGCCG | 6468 |
rs773126582 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101693094 | TTATCCCAGCCAGTG[A/G]TAAAAGAGATGCAAA | 6468 |
rs773192887 | snp | G/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101669013 | AAAGGAAACATTCCT[G/T]GAGTTTAAAGGGTAG | 6468 |
rs773227356 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101693583 | AAACGTTATTTAATG[C/T]TGTCATAATGTACTA | 6468 |
rs773230070 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101656434 | TTCATCAAGCCTACC[C/T]GCTGATCTTAAGAGA | 6468 |
rs773278829 | snp | G/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101680229 | AGGGTGAATTTAAAA[G/T]TTTAACTAGAAGAAA | 6468 |
rs773314124 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101661924 | TTTCCTCGAGTTATC[A/G]AGGTCAAGCATCCCC | 6468 |
rs773359787 | snp | C/T | 1.67139e-05 | 0.00289079 | intron-variant | FBXW4 | GRCh38.p7 | 10:101676488 | ACTTATTGCCAACCA[C/T]AGAAAATTTCATGGG | 6468 |
rs773413422 | snp | A/G | 0.00018176 | 0.00953136 | missense, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101676378 | TCCCCTCTCGGCAGC[A/G]CCCCAGTCTCCAGTT | 6468 |
rs773483123 | in-del | -/A | 1.64853e-05 | 0.00287096 | intron-variant | FBXW4 | GRCh38.p7 | 10:101667850 | TAAAAGCATTATTAT[-/A]CAGGACAAAACCACA | 6468 |
rs773494391 | snp | G/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101646115 | AGCATCAATTGGGAT[G/T]CTTGATCAAGGAAAT | 6468 |
rs773495981 | snp | G/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101657810 | GATCTGCTGATGCAT[G/T]TATTCTTTATTGTCA | 6468 |
rs773598680 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101687434 | CCACAAAATCAACAG[C/T]GTACCCTAATCCAAA | 6468 |
rs773599578 | snp | C/G | 1.6921e-05 | 0.00290865 | utr-variant-3-prime, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101611275 | CCTGGCCCAGAGGCA[C/G]GGGTGGCCCTGACGG | 6468 |
rs773615966 | in-del | -/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101648146 | GATTTGGGTTTTTTT[-/G]TTTGTTTGTTTTTTC | 6468 |
rs773646951 | snp | C/T | 1.64762e-05 | 0.00287016 | synonymous-codon, intron-variant | FBXW4 | GRCh38.p7 | 10:101667954 | GTGTAAGCACTGCCC[C/T]AGCCGGCCTGAGGCC | 6468 |
rs773705714 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101653270 | GTATTCCTGGAAAAG[A/G]ACAGCCTGTCTCTCT | 6468 |
rs773771803 | snp | A/G | 1.6552e-05 | 0.00287676 | intron-variant | FBXW4 | GRCh38.p7 | 10:101668029 | TTGCCTGGGATCAGT[A/G]GGGAGGAGAGGTGCT | 6468 |
rs773777020 | snp | A/C | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101611995 | GCAGATTATGCCTGC[A/C]CTTCTGTTTTCACAT | 6468 |
rs773792397 | snp | A/C | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101636308 | GGTGAGCCAAGATTG[A/C]GATTGAGCCACTGCA | 6468 |
rs773796040 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101670454 | ATCAGGCAAACAATA[A/G]TGGTGATTCTTATTA | 6468 |
rs773821455 | snp | C/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101645174 | CTATAGCAGAATCTA[C/G]AAAGAAAAGGGTGGC | 6468 |
rs773889798 | snp | C/T | 1.66322e-05 | 0.00288371 | missense, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101611383 | AGTACACAGGGCTGC[C/T]GAGGGGAGTCGACGT | 6468 |
rs773907681 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101675348 | GCCTAGGACAAGAAA[C/T]CAGGTTCATGCCAGG | 6468 |
rs773935292 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101660968 | GCTTAAGGAGTATCT[A/G]AAGAGAGAAAGACAG | 6468 |
rs773955516 | in-del | -/C | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101655891 | GTTCTGACCAGGCAC[-/C]CACAGCTTGGACCCA | 6468 |
rs773961103 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101674082 | CACCTGTAATCCTAG[C/T]ACTTTGGGAGGCCAA | 6468 |
rs773968510 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101623642 | CTGTACGTGTTGTAA[C/T]AGCTTTAGTTGCAAT | 6468 |
rs774028377 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101634825 | AGTTTTATAATCTTG[A/G]AAAGACATTCTTAAG | 6468 |
rs774063674 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101637953 | AATTTTTCAAAAAAC[A/G]GATATTACCCAGTAC | 6468 |
rs774069901 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101621874 | CCAAGGTTTTCAGAT[A/G]TTTAAAAGTCTGTTC | 6468 |
rs774097575 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101668974 | CACACAAAACTCAGG[C/T]AGGACCTTAGATGGA | 6468 |
rs774121423 | snp | A/C/T | 3.32029e-05 | 0.00407438 | splice-acceptor-variant | FBXW4 | GRCh38.p7 | 10:101673048 | CCAATCTTCCCATCC[A/C/T]TAGGAGAGAAATAAG | 6468 |
rs774202270 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101646169 | TGTTCCCCTGCAGTA[C/T]GGGGTAAGAAGTGAG | 6468 |
rs774221255 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101690190 | AGAATTTGCAGATAG[C/T]GCTCCTGTTCTTCCC | 6468 |
rs774225350 | snp | A/G | 1.69169e-05 | 0.00290829 | intron-variant | FBXW4 | GRCh38.p7 | 10:101611776 | ACACATTTCCTGTCC[A/G]GGAAGAGGAGAAGCA | 6468 |
rs774229163 | snp | C/T | 1.66527e-05 | 0.00288549 | intron-variant | FBXW4 | GRCh38.p7 | 10:101676471 | ATAATCCAATCACTA[C/T]AACTTATTGCCAACC | 6468 |
rs774279870 | snp | A/G | 1.73297e-05 | 0.00294356 | missense, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101612350 | ACCGGACGCTGGTGC[A/G]GAGGTCCCAGTAGCG | 6468 |
rs774292992 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101616627 | GGGAGATGGCCCAGG[C/T]GGCAGGAGCAGCAAC | 6468 |
rs774297710 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101618098 | CTGTGTGCAGGACAC[A/G]GCTTCCTTCTCCAGA | 6468 |
rs774390490 | snp | C/T | 1.65272e-05 | 0.0028746 | missense, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101676371 | AGCAGAATCCCCTCT[C/T]GGCAGCGCCCCAGTC | 6468 |
rs774422824 | snp | C/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101693465 | TACTATGTACCTATT[C/G]TGTTAGGATCAGTAA | 6468 |
rs774492232 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101641676 | TTAAGTGTGTCCCCC[C/T]AAACCCTCTCACTCT | 6468 |
rs774510981 | in-del | -/ATGA | 1.64747e-05 | 0.00287003 | intron-variant | FBXW4 | GRCh38.p7 | 10:101624732 | AGCCAGCATGGGCTC[-/ATGA]ATCTCTTACCTGTTG | 6468 |
rs774533280 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101656931 | CCCCCCTACACTTTT[C/T]TGTGCCCATTTATGT | 6468 |
rs774554504 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101611974 | CGCCATGGCCCAGAC[A/G]ACACAGCAGATTATG | 6468 |
rs774581928 | snp | G/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101639934 | TATTTATGTGAATTT[G/T]AATTTGGTTTCTGTC | 6468 |
rs774605249 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101675736 | GTAGAGAGTCAAATA[A/G]TAACTATGAAATCAT | 6468 |
rs774613988 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101670305 | CTACTTATTATCTTT[A/G]ATCTTAATGGTAACT | 6468 |
rs774617473 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101677798 | CTCTAAAAAAAAAAA[A/G]AGAGAAAAGAAATAC | 6468 |
rs774617899 | snp | G/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101678864 | GGCAGGCAGAAAGAA[G/T]ATACCTAATTCACTT | 6468 |
rs774657972 | snp | A/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101656322 | ATCCAGAGGCAACAC[A/T]GACATAAGTGTCTCC | 6468 |
rs774669831 | snp | A/G/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101628315 | GGACATCAAATCTGT[A/G/T]CTGAACAGACAGAGG | 6468 |
rs774717645 | snp | G/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101682539 | TAAAATTAATGAGTG[G/T]TGATGAAACTAAAAA | 6468 |
rs774738078 | in-del | -/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101673864 | TAGAGTAACTGAGCC[-/T]TGTGGTGATCTAAAC | 6468 |
rs774759645 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101626772 | GAATTACAGGCGTGA[A/G]CCAACGCGCCCGGCC | 6468 |
rs774789668 | snp | A/C | 1.65542e-05 | 0.00287695 | intron-variant | FBXW4 | GRCh38.p7 | 10:101624855 | TCTGGCTTGTCAGAA[A/C]CTGTGGTGGAAATGG | 6468 |
rs774796719 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101613380 | TTCCACAGAATGACT[A/G]GGGGAAATGAAGGAA | 6468 |
rs774896213 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101663352 | CACAAGGAGTGAGGT[A/G]AAAGGGTGAGAAGGG | 6468 |
rs774929118 | snp | C/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101649139 | AAGCTAATAATGAAG[C/G]ATGCTGAACTCCAAT | 6468 |
rs774947022 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101658102 | GAATTCCTATTCTTG[A/G]GCCTTAAGCCCATTA | 6468 |
rs774952969 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101621575 | GGTACTAGTTTGGGT[A/G]GGAAGGAAGAGCAGG | 6468 |
rs775026975 | snp | A/C | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101645360 | ACGGTTTGCTCAGAA[A/C]AACTGGCTTGGCTCC | 6468 |
rs775032387 | snp | A/G | 1.66946e-05 | 0.00288912 | intron-variant | FBXW4 | GRCh38.p7 | 10:101672876 | CCCCTCCCTATAGAC[A/G]GGAGGGAGTAATAGT | 6468 |
rs775033563 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101686916 | AACACACATACCACC[C/T]ATATCTGAACCTTGA | 6468 |
rs775064382 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101673920 | CAAAATTAAAAGACC[A/G]ACTAAATACCACTTT | 6468 |
rs775126719 | snp | C/G | 1.65976e-05 | 0.00288072 | missense, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101611751 | GTCGTGGGGCTCCTC[C/G]CACTCCATGACACAT | 6468 |
rs775141954 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101666475 | GGAGGGGTGCAGGCT[C/T]CATGGGGTGAGGAGA | 6468 |
rs775152529 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101672267 | TGTTGGGCACAAGCC[C/T]GGAGAAAGACTTCTC | 6468 |
rs775264328 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101686244 | AAAAAAGAATTTTAT[A/G]GTCAAAACATTTTGC | 6468 |
rs775347207 | snp | C/G/T | 3.29648e-05 | 0.00405974 | missense, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101673635 | TTAGCCTGGGATATG[C/G/T]ACAGAGAATCATCCT | 6468 |
rs775421302 | snp | A/C | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101659245 | GGCAAGACCCCAGGG[A/C]ATGAGGGTGTCCACC | 6468 |
rs775524382 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101630544 | CCATCTGCTAACCTC[C/T]GCCACTGACATCATT | 6468 |
rs775562242 | snp | A/G | 1.6483e-05 | 0.00287076 | synonymous-codon, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101611682 | AACACCGTAGTAGGA[A/G]GAACCTGTGGCCAGC | 6468 |
rs775582398 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101651898 | GAAAGGGGGCCGCGG[C/T]CCTCTCCCTGCAGCC | 6468 |
rs775612555 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101649188 | TTCTCCAGTTGAACA[C/T]CCCCTATAGATACAT | 6468 |
rs775622869 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101654931 | TGGGCTCAAGCAGTC[C/T]CCCCACCTCAGCCTC | 6468 |
rs775680902 | snp | C/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101683710 | TAATCTCTGAGATCA[C/G]AAAACTCCTGGAACA | 6468 |
rs775683351 | snp | A/T | | | intron-variant, downstream-variant-500B | FBXW4 | GRCh38.p7 | 10:101625339 | GGCACCAAAATGAGA[A/T]AAGGAAAAAATATGA | 6468 |
rs775685821 | in-del | -/CTT | | | cds-indel, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101672999 | TTCATGAGCCGAGTA[-/CTT]GACAGTGAAGGTGCT | 6468 |
rs775702283 | snp | A/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101616336 | CGAGCATCTTCTGTA[A/T]ACAAAGCATTGTGCT | 6468 |
rs775702999 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101689940 | CTCCCTAAACACCTA[C/T]TGTTAATTCCAGGCA | 6468 |
rs775708538 | snp | A/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101653794 | CATACTTCCCATGTG[A/T]TCTTGCACACAGCAG | 6468 |
rs775720465 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101614936 | TTAACTAGAAAACTC[C/T]AGCTCAACTGCTCTG | 6468 |
rs775798670 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101641569 | AGTGACATGTGCACA[C/T]AAACACAAAACACAA | 6468 |
rs775803134 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101668683 | GGTCTCTATCAGTCA[A/G]GAATGTACATTAGCA | 6468 |
rs775822100 | snp | G/T | 1.76571e-05 | 0.00297123 | intron-variant | FBXW4 | GRCh38.p7 | 10:101611445 | AAGTGGTAAGAGCTT[G/T]CCAAGTGGGACATGG | 6468 |
rs775824051 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101610764 | CTCACTCAGAACTGC[C/T]GGGTTCCCTTTGCTC | 6468 |
rs775833416 | in-del | -/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101681397 | CGTCTCAAAAAAAAA[-/T]AAATAATAATAATAA | 6468 |
rs775886637 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101639609 | CCCTCCCTGGCCACA[A/G]TTAATTAATCAAGAG | 6468 |
rs775901446 | snp | A/C/T | 0.00133422 | 0.025794 | intron-variant, synonymous-codon, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101694635 | CTCCCCGGCCGCCGC[A/C/T]GCCATGGCCACCCCT | 6468 |
rs775927111 | in-del | -/AGGAAAGGA | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101674574 | GGAATGAAGCCATTT[-/AGGAAAGGA]TGCTAATGTACTGAT | 6468 |
rs775928431 | snp | C/G | 5.54985e-05 | 0.00526746 | intron-variant, missense, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101694509 | GCCGAGGGCCCGCAT[C/G]TCCAGGTAGGAGCAG | 6468 |
rs775938973 | in-del | -/A | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101693372 | ATTATCTATAATAAC[-/A]AAAAGCTGAACACTA | 6468 |
rs775965586 | snp | C/T | 3.57795e-05 | 0.00422947 | intron-variant | FBXW4 | GRCh38.p7 | 10:101612522 | GCTCCACGTGGGTCA[C/T]ACACATTCGTTCCAC | 6468 |
rs776041684 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101675937 | GAAGAAGTAACTCCA[C/T]AGAGTAGAAGATTTA | 6468 |
rs776078193 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101663023 | ATCCAAGATGCTGGT[A/G]AATAAGGCACAGCAA | 6468 |
rs776104299 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101634068 | TAGTGAGCCAAGATC[A/G]CACCACTGCACTCCA | 6468 |
rs776159963 | snp | A/C | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101678058 | GTTCATGGTACAATT[A/C]ATTCAACTTTTCTGA | 6468 |
rs776182371 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101633086 | GAGTTATTCAACCTC[C/T]CTACAGCCCTGTTTC | 6468 |
rs776222446 | snp | C/T | | | synonymous-codon, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101611766 | CCACTCCATGACACA[C/T]TTCCTGTCCAGGAAG | 6468 |
rs776229555 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101666238 | ATTTGTTTTGAACAG[C/T]GACAGGTTTATAGGT | 6468 |
rs776237340 | in-del | -/A | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101671434 | GCTAAATCAGTACTT[-/A]AAACATGAAATTAAC | 6468 |
rs776255677 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101686363 | AGAGAGGGAATGTGG[C/T]GCACAGCATTTTCCC | 6468 |
rs776256121 | snp | A/G | 1.64738e-05 | 0.00286995 | missense, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101673597 | TGGCACCATCTGGAC[A/G]GAACTGGTAGGCCAG | 6468 |
rs776329149 | snp | A/C | 5.95788e-05 | 0.00545764 | intron-variant, utr-variant-5-prime, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101694655 | TGGCCACCCCTGTCC[A/C]CGCGATGTCGGCCCA | 6468 |
rs776370078 | snp | A/G/T | 0.00014833 | 0.00861078 | missense, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101611677 | CGTACAACACCGTAG[A/G/T]AGGAGGAACCTGTGG | 6468 |
rs776417928 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101619915 | CTGTCTGAGGGTGAG[C/T]AGCTGAGAGACACAC | 6468 |
rs776426637 | snp | C/G | | | upstream-variant-2KB | FBXW4 | GRCh38.p7 | 10:101695624 | GTGTTAGACGTATTT[C/G]GGGATTTGCAGTCTT | 6468 |
rs776531120 | snp | A/C | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101662274 | CTCCTTTCCCCAAAA[A/C]CCACCCGCTTACCGA | 6468 |
rs776533536 | snp | A/G | 1.66382e-05 | 0.00288424 | intron-variant | FBXW4 | GRCh38.p7 | 10:101611595 | TAATCATGAGTCCTG[A/G]CATGCTGGAGAAGAG | 6468 |
rs776555807 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101626615 | CTGCCTCAGCCTCCC[A/G]AGTTGCTGGGACTAC | 6468 |
rs776634290 | snp | A/C | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101646420 | TGAAATGCAGGGGTC[A/C]CTGTGCCAGAAGGCC | 6468 |
rs776638129 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101685920 | CTCCAAAGGCCCTTC[C/T]TTAAAATGTGTAACA | 6468 |
rs776641318 | snp | C/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101693795 | CATCCTGGACAGACT[C/G]CAGCCTCCTGCCTCA | 6468 |
rs776649576 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101657971 | TATTCTCTTTCTCCA[C/T]GGTATGAGGAAAATT | 6468 |
rs776684889 | snp | A/C | 1.64765e-05 | 0.00287019 | missense, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101673497 | ACTTACCCTCCTGCA[A/C]TAACAATATGCGAGT | 6468 |
rs776736646 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101680517 | CACCCTGTCTCCAAT[A/G]CCATATCATCCATGT | 6468 |
rs776748267 | in-del | -/ATTTT | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101683954 | GGGGCTTGGAATTTT[-/ATTTT]ATTTTATTTTAATTA | 6468 |
rs776762760 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101683143 | TACCTGAGAAGACAG[A/G]AGCAGGTACCCCTTG | 6468 |
rs776783841 | snp | C/T | 7.10896e-05 | 0.00596152 | intron-variant | FBXW4 | GRCh38.p7 | 10:101612510 | GAGTGAGAGGCTGCT[C/T]CACGTGGGTCATACA | 6468 |
rs776820994 | snp | A/C | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101630232 | GGCTTTTTATCTGAG[A/C]CTTATTACTCTCTAT | 6468 |
rs776852772 | snp | A/G | 1.66549e-05 | 0.00288568 | missense, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101612389 | TGTCATAGCCACAGG[A/G]CAGCAGTGTGAAAGG | 6468 |
rs776858803 | snp | A/C | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101652141 | CCTCCTCACCACCAG[A/C]TTCAAACACAAATGA | 6468 |
rs776873853 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101666057 | CTTCTATTCAGCCCA[C/T]GGATACCCAGGTCTG | 6468 |
rs776875252 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101614602 | GCCCCTGCTCTGCCC[A/G]CACAGCCTGGCAGGG | 6468 |
rs776907619 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101644799 | AGCTGAGCTGCCCAT[A/G]GCACAGGCCACTGCT | 6468 |
rs776909222 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101613225 | ATTCCCTCCGTGACC[A/G]CGGCAGTGGGCAGAC | 6468 |
rs776914093 | in-del | -/C | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101631462 | TACTAAAAAAAAGAG[-/C]CCTATGCAGAGAAAA | 6468 |
rs776925362 | snp | A/C | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101653388 | CCTCAAGTTAAAGTC[A/C]AACTCTGCTCTTCAA | 6468 |
rs776928234 | snp | C/T | 0.000108419 | 0.0073619 | intron-variant, missense, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101694462 | TCGCAGCTGGTGAAG[C/T]GCCGCAGCCAGCGGC | 6468 |
rs776953957 | snp | A/G | 9.88924e-05 | 0.0070311 | missense, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101672994 | TCCTGTTCATGAGCC[A/G]AGTACTTGACAGTGA | 6468 |
rs777040832 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101615330 | TCCCTTCCAACTCCC[A/G]TGGACAAAGCCCAGG | 6468 |
rs777074009 | snp | C/T | 0.000117277 | 0.0076567 | utr-variant-3-prime, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101611288 | CAGGGGTGGCCCTGA[C/T]GGTCATGGGTTTTGA | 6468 |
rs777142059 | snp | C/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101626444 | AGGCAATTGGACTCT[C/G]CAGATTTGAGGAGTG | 6468 |
rs777153585 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101639406 | TCCTATCAGACTCTT[C/T]ACTTTGTTTAAGAGT | 6468 |
rs777161038 | snp | A/G | 0.00053749 | 0.0163846 | intron-variant, synonymous-codon, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101694382 | GAGCGGACGCTTACA[A/G]GTCGGTGCCGAGCCG | 6468 |
rs777279656 | snp | G/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101690197 | GCAGATAGCGCTCCT[G/T]TTCTTCCCCTGTCAT | 6468 |
rs777319921 | snp | C/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101681125 | GGGCTTGGTGGCTCA[C/G]AACTGTGATCCCAGC | 6468 |
rs777339014 | in-del | -/CCCTTGCCCAATAT | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101687774 | TACCCTACACCCCAG[-/CCCTTGCCCAATAT]CCCTTGCCCAATATC | 6468 |
rs777390488 | snp | A/G | 5.94949e-05 | 0.0054538 | intron-variant | FBXW4 | GRCh38.p7 | 10:101673716 | AGTCATCAAGATACA[A/G]TATGAAAACTCAACT | 6468 |
rs777413725 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101664151 | AACACAGACAGATAC[C/T]TGCTTTCTCTCAGTC | 6468 |
rs777499790 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101678519 | CAAGCTCCGCCTCTC[A/G]GGTTCACATCACTCT | 6468 |
rs777504400 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101679551 | AATTAGTGCTATTGG[A/G]TTTGTATAGCAAGTT | 6468 |
rs777512916 | snp | G/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101650666 | GACACATGGATGGGG[G/T]AATCCTTTGCCAGCC | 6468 |
rs777528197 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101627845 | ACCCCCACACTCAGA[C/T]TCCTCCCTTGAGACT | 6468 |
rs777535899 | snp | A/G | 8.07852e-05 | 0.00635501 | intron-variant, missense, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101694595 | GGGCAGCCGACTCCC[A/G]AGCCGCCTCCTCCTC | 6468 |
rs777574714 | snp | A/G | 1.64751e-05 | 0.00287007 | missense, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101624772 | CAGATTCTCAGGGGT[A/G]AGAAGTGCCCGCAAC | 6468 |
rs777589630 | in-del | -/GA | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101638126 | CCTGGAAAGATACCT[-/GA]CCATATGTAAAAATA | 6468 |
rs777599588 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101686174 | GTTCTGTATTTGCAC[A/G]GCACTTGACCAGTAT | 6468 |
rs777610022 | snp | A/G | 3.29511e-05 | 0.00405887 | intron-variant | FBXW4 | GRCh38.p7 | 10:101667871 | CAAAACCACATCCAA[A/G]TATGTCTCCCTTACC | 6468 |
rs777610624 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101611545 | CCTTTCTAGGCACGT[C/T]CTTGGCTACCTCACC | 6468 |
rs777631130 | snp | A/G | 8.23621e-05 | 0.00641672 | missense, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101673573 | CTCCCAGAGGCCGAC[A/G]ATTCAAGCTGGCACC | 6468 |
rs777704352 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101687983 | GAGACAACCTCCAGC[A/G]TCATTCCCCAAAGGT | 6468 |
rs777820165 | snp | A/C | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101644421 | CTTTCTGGGAAGTGG[A/C]GACACTCAAGACAAT | 6468 |
rs777889376 | snp | C/G | 0.000105669 | 0.00726797 | intron-variant, synonymous-codon, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101694440 | GGCTATCCGGCGCCA[C/G]AGCAGATCGCAGCTG | 6468 |
rs777923927 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101621035 | CCCAGCCCGCCACCC[A/G]GCTTGTGTGTCATCC | 6468 |
rs777930539 | snp | C/T | 1.75323e-05 | 0.00296072 | intron-variant | FBXW4 | GRCh38.p7 | 10:101673092 | AGAACCAATTATTCT[C/T]TCTGTAGAAAGAGAA | 6468 |
rs777974573 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101674457 | ATACATACCTCTTCC[A/G]CAATAGATCAGTTAA | 6468 |
rs777980721 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101658936 | ATTATCATGACAAGG[C/T]CACTGGAACGGATCA | 6468 |
rs777998835 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101668558 | TCCAATACTATTCAC[A/G]TCAGCAGGGAATTTA | 6468 |
rs778049282 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101665778 | CAATAGTTGTTGTGC[C/T]CTATTCTGTTAAGAG | 6468 |
rs778069739 | snp | A/C | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101673296 | TTCACTTTTCATTAG[A/C]AGCTCTTCCTGTTTT | 6468 |
rs778086462 | snp | A/C | 1.64773e-05 | 0.00287026 | synonymous-codon, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101672975 | GCAATCCACACAGTT[A/C]ACCTCCTGTTCATGA | 6468 |
rs778191235 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101632247 | AACCCTCTCTCAACC[C/T]AAGTGCATCAGGGCA | 6468 |
rs778195616 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101631228 | TCAAAAGCTTAGCCA[A/G]CTTCACGGATGACTG | 6468 |
rs778212133 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101645430 | TGTGCCCCTGTGTCA[A/G]TCCTGTGTCTCACTT | 6468 |
rs778272272 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101683287 | CTGTAAATAAATCTC[C/T]CCGTGGATGTTAATG | 6468 |
rs778348447 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101654391 | TTTATGATATATAAA[C/T]TCTACTTCAATAAGG | 6468 |
rs778369101 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101692259 | TGAAGAGTTCAGATA[C/T]AGATCCAATATACAC | 6468 |
rs778369539 | snp | G/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101666876 | AGCCTGGTCAATATA[G/T]AAACACCCCATTTCT | 6468 |
rs778453218 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101655636 | ACAGGAGGAAAGACC[C/T]AGGTTTCTCTAGGAC | 6468 |
rs778537514 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101639361 | CTAGTAATAATGTGA[A/G]GGGGAGGAGGTCAAA | 6468 |
rs778569309 | snp | A/G | 8.27438e-05 | 0.00643157 | missense, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101611362 | GCTTGGTGGTGAGAC[A/G]CAGGCAGTACACAGG | 6468 |
rs778572035 | snp | A/C | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101677089 | CAATAAGAAACTCGC[A/C]TACATTGTTGGTGGG | 6468 |
rs778642988 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101678277 | TCATGAGCAAGAATT[C/T]GAAAATTCCACTTTA | 6468 |
rs778657797 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101691206 | GCAGCCATACTCTTG[C/T]TGTACTTTGGGCCCG | 6468 |
rs778660981 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101664060 | CTAAGCACATAACCA[A/G]TACTAAATATGATCC | 6468 |
rs778670881 | snp | C/G | 6.79844e-05 | 0.00582989 | missense, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101612451 | CCTGGGGGAAAGTCA[C/G]TGCCCAAGTGTGTCA | 6468 |
rs778676945 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101639861 | GTGTATTTCAGTTCT[A/G]CCTTTGGCTTGGTTT | 6468 |
rs778724143 | snp | C/T | 1.64743e-05 | 0.00287 | | | GRCh38.p7 | 10:101624739 | ATGGGCTCATGAATC[C/T]CTTACCTGTTGAGGT | 6468 |
rs778726647 | snp | A/C | 0.00023872 | 0.0109226 | | | GRCh38.p7 | 10:101694427 | TGAGCGAGGCCCGGG[A/C]TATCCGGCGCCAGAG | 6468 |
rs778847560 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101660595 | CTCCATGCTTCCACT[C/T]TGGGATGTGATTGCT | 6468 |
rs778897448 | in-del | -/TTGT | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101668516 | GAAGGTGGTGTGTTG[-/TTGT]TTGTTTGTTGATAAT | 6468 |
rs778935402 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101657596 | CTGAGATCATCATCA[C/T]GCCACTGTAGTCCAG | 6468 |
rs778951344 | in-del | -/C | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101678733 | GCGCCCGGCGAGATA[-/C]ACTCATTTATTCGAG | 6468 |
rs778960248 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101612900 | AGCTGCCTGAGTCCA[A/G]TGCCTTAATTCCTGC | 6468 |
rs778979679 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101649816 | CTGCCTTCCGATCCA[C/T]ATGGAAAGTGAAGAC | 6468 |
rs779019249 | snp | A/G | 1.71237e-05 | 0.00292602 | utr-variant-3-prime, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101611246 | GCAAGAGAAGTCCCT[A/G]AGTAGCTGGTTTCCC | 6468 |
rs779036004 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101619440 | GAGGCAGGTGGATCA[C/T]GAGGTCAGGAGATCG | 6468 |
rs779043597 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101620869 | TCTAGGGGTTTCATA[A/G]GAGAATAACAGTCAA | 6468 |
rs779066307 | snp | C/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101633462 | GGGGGTAGTGGGTTA[C/G]GGGAGGGATAGCATT | 6468 |
rs779149563 | snp | A/C | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101630181 | CTCTCTGACCTCTGA[A/C]AGGCACTGACACGAG | 6468 |
rs779173226 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101686081 | AGCACTAAGCATAAC[C/T]CTGGGTCCTTTATGT | 6468 |
rs779175625 | snp | A/G | | | upstream-variant-2KB | FBXW4 | GRCh38.p7 | 10:101695491 | TCTTCCTCGAGTGAT[A/G]CCTCCTTTCCACGGG | 6468 |
rs779196296 | snp | C/T | 0.000131811 | 0.00811715 | missense, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101672956 | TCACAATGATGCCCC[C/T]TTTGCAATCCACACA | 6468 |
rs779204544 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101664699 | CAGCAGTTGAAGCCA[C/T]TAAGCAAATGCTACA | 6468 |
rs779212344 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101672820 | TCCCCTGTCCCCAGA[C/T]GATACTCTCAGCCAA | 6468 |
rs779287067 | in-del | -/ACAC | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101624092 | CATAGACACAGACAG[-/ACAC]ACACACACACACACA | 6468 |
rs779302155 | snp | C/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101671093 | GAATTTCAGATGCCA[C/G]TGAAAAGAAATGATG | 6468 |
rs779304887 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101644221 | TGGGAACGGTGAGCT[A/G]GAGCTGCTCTGTGCA | 6468 |
rs779321854 | snp | A/C | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101685212 | ACTCTTCCAAACATG[A/C]CATCTGAACTGTTAG | 6468 |
rs779326459 | in-del | -/AC | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101632213 | ACACATATTCTCTAC[-/AC]ACACACACACACACA | 6468 |
rs779376271 | snp | A/G | | | upstream-variant-2KB | FBXW4 | GRCh38.p7 | 10:101695322 | GAGAGCGCTTGGTGG[A/G]AGCACAGGAGTTCGC | 6468 |
rs779393331 | in-del | -/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101691839 | AGACTGCATGCCCAA[-/G]AAGTCCCAAGGAACC | 6468 |
rs779425385 | snp | A/T | | | upstream-variant-2KB | FBXW4 | GRCh38.p7 | 10:101696627 | CCAAATGCAACAAAG[A/T]CTTTGTGTAGAAAAC | 6468 |
rs779544066 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101630897 | CATCCACCTGAATGC[C/T]CTCTAGAGCGCAGCT | 6468 |
rs779551762 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101614268 | TTCATGTTTGTTTGA[A/G]ATAGAAGATGAAAGG | 6468 |
rs779595877 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101668048 | AGGAGAGGTGCTCCG[A/G]GAGAGGTGACTGTTG | 6468 |
rs779625496 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101689625 | ACTTTGAGTTGTTAA[C/T]TGTTTTCTGAAGATC | 6468 |
rs779631751 | snp | A/C/T | 0.000266276 | 0.0115355 | intron-variant, missense, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101694421 | CGGAGTTGAGCGAGG[A/C/T]CCGGGCTATCCGGCG | 6468 |
rs779763429 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101647265 | TCTCACCCACAGGTC[A/G]TTCTGCCCCCATCAG | 6468 |
rs779809603 | snp | C/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101639495 | TCATGGAGTCATTTG[C/G]CCTTTATCCAACTAG | 6468 |
rs779869653 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101613885 | TCTGGTCTTCCTCTC[A/G]GTAGCCCAGAGCTGG | 6468 |
rs779873105 | in-del | -/C | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101669190 | AAGAAAATAAACATA[-/C]TAAGAGGATCCTAAA | 6468 |
rs779970926 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101648249 | AGCAAAGGACAGGTT[A/G]GGAGGAAAAAAGCAA | 6468 |
rs780090144 | snp | C/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101625975 | GAAGCCAGTGGCTTT[C/G]GCTGGGGTGGGGAGG | 6468 |
rs780152779 | in-del | -/C | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101629289 | AGTAGGTACCACTTT[-/C]CCTTTTTTTTTTTGA | 6468 |
rs780162323 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101684695 | TTTAGTGTAAAGTAT[C/T]TAAGCAGCCAAAGAT | 6468 |
rs780166282 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101656030 | CACACATCTCAGCTT[C/T]TTCTTCAGCCAATGC | 6468 |
rs780222598 | in-del | -/GGGT | 1.6921e-05 | 0.00290865 | utr-variant-3-prime, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101611275 | CTGGCCCAGAGGCAG[-/GGGT]GGGTGGCCCTGACGG | 6468 |
rs780270910 | snp | C/T | 1.65037e-05 | 0.00287256 | intron-variant | FBXW4 | GRCh38.p7 | 10:101668005 | GGAGAGGAGATGCTC[C/T]CGTTGGCATTGCCTG | 6468 |
rs780279849 | snp | C/T | 1.64925e-05 | 0.00287158 | missense, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101611711 | GCAGGTGGTTGCCAT[C/T]TGTCTGCAGGCAGTA | 6468 |
rs780365225 | in-del | -/CCT | 0.0155373 | 0.0867598 | intron-variant, cds-indel, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101694601 | CCGACTCCCGAGCCG[-/CCT]CCTCCTCCTCCTCCT | 6468 |
rs780377242 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101633375 | CAAACACTGCATGTT[C/T]TCATAACTGGGAGCT | 6468 |
rs780379493 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101617811 | TTTCAAAGAGTTCAG[A/G]GGGACAGAGGAGACA | 6468 |
rs780388856 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101623931 | AATCAGGGACAATGG[A/G]AAGAGGAGGAGGGGA | 6468 |
rs780430348 | snp | C/T | 1.64741e-05 | 0.00286998 | synonymous-codon, intron-variant | FBXW4 | GRCh38.p7 | 10:101667930 | GACTCGGTCTTCAGT[C/T]TGGATGGTGTGTAAG | 6468 |
rs780452583 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101656056 | AATGCATGTCACCTG[C/T]GCACTGAAACCCCAC | 6468 |
rs780525366 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101671011 | AAAAATAGATGGTTA[C/T]AGGCAAATATCACTG | 6468 |
rs780546659 | in-del | -/TTTTT | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101640485 | CTTTCTTTCTTTCTC[-/TTTTT]TTTTTTTTTTTTTTT | 6468 |
rs780553686 | snp | C/T | 1.79065e-05 | 0.00299215 | intron-variant | FBXW4 | GRCh38.p7 | 10:101612330 | CCTCCCTGCCCAGCA[C/T]ACTCACCGGACGCTG | 6468 |
rs780572665 | snp | C/T | 3.29457e-05 | 0.00405854 | missense, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101673561 | GCCCAGCAAAGACTC[C/T]CAGAGGCCGACGATT | 6468 |
rs780584430 | snp | C/T | | | intron-variant, missense | FBXW4 | GRCh38.p7 | 10:101628001 | TGTTCGATTTGAATC[C/T]GCGAGATGTCTTCAA | 6468 |
rs780587721 | in-del | -/AA | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101637703 | AGATCCTGTCTCAAA[-/AA]AAAAAAAAAAAAAAA | 6468 |
rs780627881 | snp | C/G | 6.59533e-05 | 0.00574215 | synonymous-codon, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101611649 | GCAGGCCCTTTGACG[C/G]CGGTCCCACAGCCGT | 6468 |
rs780697478 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101643977 | CAAAGCCTAATTGAC[C/T]TACTGAAGTTTAACA | 6468 |
rs780841859 | snp | A/C | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101637063 | TTTTGTATATTTTGA[A/C]AATTTCCGTTATAAA | 6468 |
rs780854428 | snp | C/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101650895 | CAAAGATCGGGCTCT[C/G]GAGAGACGCGGCCTG | 6468 |
rs780858814 | snp | C/T | 1.66885e-05 | 0.00288859 | intron-variant | FBXW4 | GRCh38.p7 | 10:101676287 | CCAGATTTTTTACTT[C/T]CCATTATGCTTTTAT | 6468 |
rs780918703 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101679844 | CAGTCACCTGAATAG[C/T]GTACACTGTACCCAG | 6468 |
rs780992506 | snp | C/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101647017 | AAGCATGGCTTCAGT[C/G]AGCGATACCACAAAA | 6468 |
rs781004014 | in-del | -/CCTCCT | | | intron-variant, cds-indel, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101694601 | CCGACTCCCGAGCCG[-/CCTCCT]CCTCCTCCTCCTCCT | 6468 |
rs781008235 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101688381 | TGTGCTGGCAATTAA[C/T]TGTGGGCTAAAGAGG | 6468 |
rs781116078 | snp | G/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101674780 | TGCAATCTGACAGGA[G/T]GAAGAAAGGCTAGAA | 6468 |
rs781123938 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101636582 | TAATGGTATTATGAT[C/T]ACTATCTTTTTTTTT | 6468 |
rs781133068 | snp | A/C | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101689485 | ATAGAAACCATTAAA[A/C]ATAAGGCCTTTCCAA | 6468 |
rs781153285 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101622982 | AAACAATCCAGCAGG[C/T]AAAAGACATGAACAG | 6468 |
rs781177654 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101672185 | CTCCTGCACCACCAA[C/T]TGAATTGTCAGCAAA | 6468 |
rs781216538 | snp | A/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101683417 | AGCTTTCCGGCACTT[A/T]GTAACCATTAGAGTT | 6468 |
rs781234377 | snp | C/G/T | 3.2948e-05 | 0.00405871 | missense, intron-variant | FBXW4 | GRCh38.p7 | 10:101667919 | GCAATGGACCAGACT[C/G/T]GGTCTTCAGTCTGGA | 6468 |
rs781269292 | in-del | -/AAAA/AAAAA/AAAAAA | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101641631 | GTAAGATTTTTTCTC[-/AAAA/AAAAA/AAAAAA]AAAAAAAAACAAAAC | 6468 |
rs781292781 | snp | A/G | 1.64901e-05 | 0.00287137 | intron-variant | FBXW4 | GRCh38.p7 | 10:101667994 | ACCTAGAAACAGGAG[A/G]GGAGATGCTCTCGTT | 6468 |
rs781303866 | in-del | -/A | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101638489 | TACTGGATGTCCTGC[-/A]AAAAAAAAAAAAAAA | 6468 |
rs781385184 | snp | G/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101645811 | AGAGAGCTCAGCACA[G/T]GACAGGCAAGCAGAC | 6468 |
rs781389783 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101660148 | GAAAGCACAGGTCAG[A/G]TAAGAGGAGAAAGAG | 6468 |
rs781398724 | snp | A/G | 4.94173e-05 | 0.00497053 | synonymous-codon, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101673535 | CACAAAGTGGCAAAC[A/G]TCCTCATCATGCCCA | 6468 |
rs781525062 | snp | A/C/G | 5.26758e-05 | 0.00513182 | intron-variant | FBXW4 | GRCh38.p7 | 10:101611441 | CAGGAAGTGGTAAGA[A/C/G]CTTTCCAAGTGGGAC | 6468 |
rs781576285 | snp | A/G | 1.65121e-05 | 0.00287329 | synonymous-codon, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101611634 | GACACTTACGTGCAG[A/G]CAGGCCCTTTGACGC | 6468 |
rs781598737 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101668534 | TTTGTTTGTTGATAA[C/T]GCCCAGGATCCAATA | 6468 |
rs781603074 | snp | A/C | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101619037 | CCCTGGGGCCTAGCC[A/C]AGGAAGGGTCCTGCT | 6468 |
rs781619892 | snp | A/C | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101617360 | CCCCAAGAGTTACCC[A/C]GGGTCACCTCCAGCC | 6468 |
rs781631375 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101655715 | CACCCTGCATGAGTC[A/G]AGTCCTTGGGAGAAA | 6468 |
rs781666632 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101658734 | TGTTACTAATCCAGC[C/T]ACAACCTCATTATTG | 6468 |
rs781670851 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101684452 | TTTTTGTATGTTTAA[C/T]AGAGATGGGGTTTCA | 6468 |
rs781687538 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101623099 | ATTCAAATTAAAACA[C/T]GATGAAATATAACAC | 6468 |
rs796094706 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101679795 | GGTTACATGGATGAA[C/T]TGTACAATGATGAAG | 6468 |
rs796124613 | snp | A/C | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101683004 | TATTGGCTTCAGCAC[A/C]TGAAAAATCCAAAGA | 6468 |
rs796132910 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101644980 | CACATGGTTTGTAGG[C/T]GGTGGTCAGGTCACA | 6468 |
rs796176903 | in-del | -/AT | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101681400 | TCTCAAAAAAAAAAA[-/AT]AATAATAATAATAAT | 6468 |
rs796178456 | snp | C/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101618408 | TCATTAGGCACAGAG[C/G]GGGTATTCTGGGCAT | 6468 |
rs796185716 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101632040 | TAGTGTTAGCAACCA[C/T]GGCCCTGGTACACCT | 6468 |
rs796223454 | in-del | -/A | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101686674 | TTGTTTTTAATCATG[-/A]AAACTGTGTTCTATA | 6468 |
rs796244141 | snp | C/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101651374 | GGAGAGAAAGCCACA[C/G]GATACATTTCAAAGT | 6468 |
rs796282917 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101642990 | TCCCTCCCTGCCATC[C/T]TCCCCAAATAATATA | 6468 |
rs796365673 | snp | A/C | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101688525 | AACAGGAGATAAATT[A/C]TTTCTCCAGATAGTC | 6468 |
rs796433194 | snp | C/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101624659 | CCTTCTCCTGGACCA[C/G]TCAGCCAACTGAGGC | 6468 |
rs796447684 | in-del | -/AATAATAATAAC | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101681757 | AATAATAATAATAAT[-/AATAATAATAAC]AACAGGTCTAAAGAT | 6468 |
rs796460507 | in-del | -/AG | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101685982 | CTAAATTCTTATTCT[-/AG]AGAGGCTCAAGGGAA | 6468 |
rs796571941 | snp | A/G | | | missense, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101673509 | GCACTAACAATATGC[A/G]AGTTGGCCAGCACAA | 6468 |
rs796596394 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101675805 | GTGCCACAGGCATTT[C/T]CTAAATTTCCTTATA | 6468 |
rs796599540 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101662358 | TGAAGCAAGAAGGGG[C/T]AGCTCCTCCATCAAA | 6468 |
rs796603245 | snp | G/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101668919 | AGGCAGCCAGATGGA[G/T]CAGTGACCTCTTAAG | 6468 |
rs796752957 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101671019 | ATGGTTACAGGCAAA[C/T]ATCACTGCAAATTCT | 6468 |
rs796763635 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101633170 | ATTATATGGGAAGTA[C/T]AAATTAGTTCAACCA | 6468 |
rs796774198 | in-del | -/AA | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101636003 | AACAAGTAATTTATG[-/AA]AAAAAATATACATGG | 6468 |
rs796801069 | snp | C/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101684908 | GTAGGAAACATGCCA[C/G]CATGAGGACAAGACC | 6468 |
rs796815270 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101683675 | GAAGTGTAGGTATAT[C/T]GAAGAGGTCTTAAAC | 6468 |
rs796893297 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101620729 | GCGATCCTACTGCCT[C/T]AGTCTCTCAAAGTGC | 6468 |