SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs14279 | snp | C/T | 0 | 0 | utr-variant-3-prime | CUL4B | GRCh38.p7 | X:120524806 | AAACTTGATGCTGTT[C/T]CAGCTGAAAAATTAG | 8450 |
rs1057116 | snp | A/G | 0.150308 | 0.229263 | utr-variant-3-prime | CUL4B | GRCh38.p7 | X:120526086 | GAGTATGGGATGTGT[A/G]TATATGGCTTAGCCC | 8450 |
rs1801846 | snp | A/G | | | utr-variant-3-prime | CUL4B | GRCh38.p7 | X:120525756 | ATTTTCTCTACCAAA[A/G]TTTTTTTTAGAAGCA | 8450 |
rs2106543 | snp | C/G | 0.490329 | 0.0688607 | intron-variant | CUL4B | GRCh38.p7 | X:120570228 | GTGAGAATCACAAAG[C/G]GGGAGAATAGGGTTT | 8450 |
rs2285549 | snp | C/T | 0.0555816 | 0.157167 | intron-variant | CUL4B | GRCh38.p7 | X:120544033 | TGTTGGGAAGATAAA[C/T]GCAAAGGGAAGCTTA | 8450 |
rs2285550 | snp | A/G | 0.362309 | 0.223353 | upstream-variant-2KB, intron-variant | CUL4B | GRCh38.p7 | X:120561769 | GGAGTAACCCTAAAT[A/G]GAGGAAAACATAATC | 8450 |
rs2285551 | snp | A/G | 0.000529661 | 0.016265 | upstream-variant-2KB, intron-variant | CUL4B | GRCh38.p7 | X:120562546 | AATTTCCATAACAAT[A/G]ATATGACATATATAC | 8450 |
rs2301636 | snp | C/T | 0.451229 | 0.148347 | intron-variant, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120557736 | AAGCACAACTTATAC[C/T]GGTATGACTGTACCC | 8450 |
rs3214123 | in-del | -/AT | | | intron-variant | CUL4B | GRCh38.p7 | X:120543702 | CGACAGTTTAAGACT[-/AT]TAAATTCAGCATGTG | 8450 |
rs3747434 | snp | A/G | 0 | 0 | synonymous-codon | CUL4B | GRCh38.p7 | X:120537005 | CACAGTTAACTCAAT[A/G]TTTCCCGGAACATTC | 8450 |
rs4360414 | snp | C/T | 0.499734 | 0.0115201 | intron-variant | CUL4B | GRCh38.p7 | X:120528232 | GCTAACATGGCAAAA[C/T]CCCATCTGTACTAAA | 8450 |
rs4495565 | snp | A/C | 0 | 0 | intron-variant | CUL4B | GRCh38.p7 | X:120570732 | ATAATGAAATACTAT[A/C]CAGCATTGAACAATG | 8450 |
rs5909729 | snp | C/T | 0.0168099 | 0.0901243 | upstream-variant-2KB, intron-variant | CUL4B | GRCh38.p7 | X:120563436 | GAGTCAGGGTTTTGC[C/T]ATGTTGGCCAGGCTG | 8450 |
rs5909731 | snp | A/T | 0.245924 | 0.249967 | upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120576347 | TTTCTGCATGTTTGA[A/T]CATTTTTATAACAAA | 8450 |
rs5909732 | snp | A/C | 0.254536 | 0.249959 | upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120577657 | TCTATACTCATTGCA[A/C]TCATTTATAAGGAAT | 8450 |
rs5910904 | snp | C/T | 0.441884 | 0.160251 | intron-variant | CUL4B | GRCh38.p7 | X:120548748 | CTGAGGCAGGAGAAT[C/T]GCTTGAACCCAGGAG | 8450 |
rs5910908 | snp | C/T | 0.420529 | 0.182811 | upstream-variant-2KB, intron-variant | CUL4B | GRCh38.p7 | X:120563169 | CGCTGAGAAGGGAGA[C/T]GGGGGCCTGAAAGGA | 8450 |
rs5910909 | snp | C/T | 0.286116 | 0.247378 | intron-variant | CUL4B | GRCh38.p7 | X:120564353 | gctcaggcttgtaat[C/T]ccaaaactttgggag | 8450 |
rs5910915 | snp | C/T | 0.254536 | 0.249959 | upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120577355 | tgtctgtaattccag[C/T]gctttgggaggccga | 8450 |
rs5910916 | snp | A/G | 0.078261 | 0.181675 | upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120577369 | gcgctttgggaggcc[A/G]aggtaggtggattga | 8450 |
rs5956224 | snp | A/C | 0.109764 | 0.206963 | intron-variant | CUL4B | GRCh38.p7 | X:120535123 | tagcttgagcccatg[A/C]gtttgaggttacagt | 8450 |
rs5956225 | snp | A/G | 0.132653 | 0.220748 | intron-variant | CUL4B | GRCh38.p7 | X:120552127 | catattatgcattac[A/G]tatttattatttaCA | 8450 |
rs5956226 | snp | C/T | 0.440613 | 0.161761 | intron-variant, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120558779 | AAGTTTTAATTAGAA[C/T]ATCCAAATGCCTTAA | 8450 |
rs5957406 | snp | C/T | 0.110699 | 0.207594 | intron-variant | CUL4B | GRCh38.p7 | X:120526946 | AAAAGACAACAGTTT[C/T]GGCTCATGAATTTAA | 8450 |
rs5957407 | snp | C/T | 0.0768 | 0.180282 | intron-variant | CUL4B | GRCh38.p7 | X:120540702 | aagatggaatcttgc[C/T]atgttgcccaggcta | 8450 |
rs5957408 | snp | C/T | 0.0983752 | 0.198771 | intron-variant | CUL4B | GRCh38.p7 | X:120543829 | AAAGATAGTTTTTTA[C/T]ATTATTGTTTTCCTC | 8450 |
rs5957411 | snp | A/G | 0.0560809 | 0.157783 | upstream-variant-2KB, intron-variant | CUL4B | GRCh38.p7 | X:120563164 | AGAACCGCTGAGAAG[A/G]GAGATGGGGGCCTGA | 8450 |
rs5957412 | snp | A/G | 0.0831127 | 0.186141 | upstream-variant-2KB, intron-variant | CUL4B | GRCh38.p7 | X:120563186 | GGGGCCTGAAAGGAG[A/G]CAGATGGAAGCACTC | 8450 |
rs6603633 | snp | A/C | 0.110232 | 0.207279 | intron-variant | CUL4B | GRCh38.p7 | X:120530932 | CATAAATGTTTTAAA[A/C]GTAAGGACATGGTAA | 8450 |
rs6645657 | snp | C/T | 0.139594 | 0.2243 | intron-variant | CUL4B | GRCh38.p7 | X:120546951 | TACATGAATACCACA[C/T]GTAGTCCTGGACACG | 8450 |
rs6646682 | snp | A/C | 0.0550819 | 0.156547 | intron-variant | CUL4B | GRCh38.p7 | X:120544963 | TCTAAGACATAAAAC[A/C]GTTTTCACTGTACTG | 8450 |
rs6646683 | snp | C/T | 0 | 0 | intron-variant | CUL4B | GRCh38.p7 | X:120553451 | TTCACAAAAAGGTAA[C/T]TACAGTTCCCattat | 8450 |
rs6655533 | snp | A/G | 0.112567 | 0.208835 | intron-variant, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120559365 | TAATACTCTCCTCAC[A/G]TATCTCAAACACGGT | 8450 |
rs7049515 | snp | C/T | 0.405517 | 0.195741 | intron-variant | CUL4B | GRCh38.p7 | X:120569383 | TTTTTTTTTTTGAGA[C/T]GGAGTCTCGCTCTGT | 8450 |
rs7057136 | snp | C/T | 0.0328205 | 0.123827 | intron-variant | CUL4B | GRCh38.p7 | X:120536509 | CCTATGGGTGAAATA[C/T]GTGCAAGAATTCTTA | 8450 |
rs7879339 | snp | A/G | 0.0699487 | 0.17344 | intron-variant | CUL4B | GRCh38.p7 | X:120566369 | TATATATATATATAT[A/G]TATATATATATATAT | 8450 |
rs7879694 | snp | A/G | 0.485039 | 0.0851863 | intron-variant | CUL4B | GRCh38.p7 | X:120573857 | ttgagacggagtccc[A/G]ctgttgcccaggctg | 8450 |
rs7881300 | snp | A/G | 0 | 0 | intron-variant | CUL4B | GRCh38.p7 | X:120549634 | CACCACACCTCATCA[A/G]GAAACAGCAGGCCAA | 8450 |
rs11549411 | snp | G/T | 0.0116955 | 0.0755709 | utr-variant-3-prime | CUL4B | GRCh38.p7 | X:120524709 | GAACAACAACTGAAA[G/T]TCACAATTATCCAAT | 8450 |
rs11796393 | snp | C/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120536521 | ATATGTGCAAGAATT[C/T]TTAATAGCTAGGTAG | 8450 |
rs11796939 | snp | A/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120538437 | AAAATAAATGGGAAA[A/T]TTTTATACAAATAAT | 8450 |
rs12011507 | snp | G/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120569563 | gacggggtttcaccg[G/T]gttagccaggatggt | 8450 |
rs12387747 | snp | C/T | 0.0879364 | 0.190356 | intron-variant | CUL4B | GRCh38.p7 | X:120530961 | AATCCTTTAAGAAAA[C/T]ATCCTGTCTTTGATG | 8450 |
rs12392620 | snp | A/C | 0.108827 | 0.206325 | intron-variant | CUL4B | GRCh38.p7 | X:120574106 | ccatcacctgccccc[A/C]tctgccccagcctcc | 8450 |
rs12393998 | snp | A/C | 0.491747 | 0.063706 | intron-variant | CUL4B | GRCh38.p7 | X:120566227 | CAATGTGAATTCATC[A/C]GTTTCCCATCCTGAG | 8450 |
rs12396563 | snp | C/G | 0.149865 | 0.22907 | intron-variant | CUL4B | GRCh38.p7 | X:120552013 | TGAAAAGCACTttta[C/G]aaatatattctttta | 8450 |
rs12688345 | snp | C/T | 0.49952 | 0.0154892 | intron-variant | CUL4B | GRCh38.p7 | X:120530690 | CATGGTATTAACTGG[C/T]TAAGCAAACTAGTTA | 8450 |
rs12837257 | snp | A/T | 0 | 0 | upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120577152 | CTTTTCTCTTTCTTT[A/T]AGATTTATACAGCTT | 8450 |
rs12839503 | snp | A/G | 0.0912962 | 0.193166 | intron-variant | CUL4B | GRCh38.p7 | X:120571097 | tgctctaggggaagt[A/G]tgggaggaaaattta | 8450 |
rs12842985 | snp | C/T | 0.0490645 | 0.148745 | intron-variant | CUL4B | GRCh38.p7 | X:120575365 | TTCCTAAACAAGATC[C/T]TCCCCACATTCCGAA | 8450 |
rs12858999 | snp | C/T | 0 | 0 | upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120576112 | ttgctagattgctcc[C/T]ttttgggttctttgt | 8450 |
rs17853573 | snp | G/T | 0.0110494 | 0.0735024 | missense | CUL4B | GRCh38.p7 | X:120535865 | ACACACAGTGTCCTA[G/T]GGTTGACTGCCACTG | 8450 |
rs28460170 | snp | A/C | 0.108827 | 0.206325 | intron-variant | CUL4B | GRCh38.p7 | X:120572622 | ATTAAAGATCTTTTT[A/C]TATACACTTAACCAA | 8450 |
rs28528673 | snp | A/T | 0.108827 | 0.206325 | intron-variant | CUL4B | GRCh38.p7 | X:120573129 | GTTAAATTTGGTGCA[A/T]CACCTTCCTCAGCAT | 8450 |
rs28590057 | snp | A/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120548339 | GCTTCATTTTGGGTT[A/T]AAAAAAGAATTTCAC | 8450 |
rs34111189 | snp | A/G | 0.0505727 | 0.150761 | intron-variant | CUL4B | GRCh38.p7 | X:120566020 | GGCGTGAGCCACCGC[A/G]CCCGGCCCAGGCAGT | 8450 |
rs34722195 | in-del | -/A | | | intron-variant | CUL4B | GRCh38.p7 | X:120543052 | AAGGAAAAAAAAAAA[-/A]GGTTAGTATTATTGA | 8450 |
rs34777683 | in-del | -/G | | | intron-variant | CUL4B | GRCh38.p7 | X:120536115 | ACCAAATCAAATGGG[-/G]ATTTATTAGGATTTA | 8450 |
rs34930174 | in-del | -/C | | | intron-variant | CUL4B | GRCh38.p7 | X:120570907 | AAGTATAGAAGGAAA[-/C]ATAGCTGGGTGATAT | 8450 |
rs35048954 | snp | C/T | 0.00202198 | 0.0317317 | intron-variant | CUL4B | GRCh38.p7 | X:120546638 | CATATGTTAAGGATA[C/T]TTTAAAGCGTTTGGT | 8450 |
rs35267132 | in-del | -/C | | | utr-variant-3-prime | CUL4B | GRCh38.p7 | X:120526446 | AAGAACCCTCCCCCC[-/C]TTTTTAATAGCCACA | 8450 |
rs35644958 | in-del | -/G | | | intron-variant | CUL4B | GRCh38.p7 | X:120555666 | TGGGGATAGGCCAGG[-/G]CGCGGTGGCTCACAC | 8450 |
rs35746806 | in-del | -/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120543704 | ACAGTTTAAGACTAT[-/T]AAATTCAGCATGTGG | 8450 |
rs35976026 | in-del | -/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120543999 | AAGGAGCACCTAAGT[-/T]GAGAGAAGAGCATCA | 8450 |
rs45437794 | snp | C/T | 0.0317957 | 0.122012 | utr-variant-5-prime | CUL4B | GRCh38.p7 | X:120575712 | CCAAAGCCTGGGTTA[C/T]TCTCTAATAATACTA | 8450 |
rs45524842 | snp | A/G | 0.0204488 | 0.0990265 | utr-variant-5-prime | CUL4B | GRCh38.p7 | X:120575744 | CTATGGGACTTAAAC[A/G]GATAAGCCTAGGTTG | 8450 |
rs45549338 | snp | A/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120540703 | AGATGGAATCTTGCT[A/T]TGTTGCCCAGGCTAG | 8450 |
rs55848212 | snp | C/T | | | utr-variant-3-prime | CUL4B | GRCh38.p7 | X:120524970 | CATCTCACAGACCAT[C/T]AGGGATGAGTTAGAA | 8450 |
rs56016419 | snp | A/G | 0.00581083 | 0.0535878 | intron-variant | CUL4B | GRCh38.p7 | X:120534350 | ACAGAGTGAGACCCT[A/G]TCTCATTAAAAAAAA | 8450 |
rs56144145 | snp | G/T | 0.255278 | 0.249944 | intron-variant | CUL4B | GRCh38.p7 | X:120570738 | AAATACTATACAGCA[G/T]TGAACAATGAATAAA | 8450 |
rs56241821 | snp | A/G | 0.39608 | 0.202881 | intron-variant | CUL4B | GRCh38.p7 | X:120554724 | TCAGAGAAAGAGGGT[A/G]GGACAGGGGTTTGGA | 8450 |
rs57119187 | snp | C/G | | | intron-variant | CUL4B | GRCh38.p7 | X:120539056 | TATTTAAGAGATTAA[C/G]CCAAGTAGCAAAAAT | 8450 |
rs58096878 | snp | A/C | 0.0261392 | 0.111294 | utr-variant-3-prime | CUL4B | GRCh38.p7 | X:120525918 | TTACAAAACACGTTC[A/C]TTTTGGTCTCTTTTG | 8450 |
rs58242779 | snp | C/T | | | intron-variant, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120557845 | AGTCTACTTAAGAAC[C/T]TATTTCAGAAAGCAA | 8450 |
rs58763492 | in-del | -/GT | | | intron-variant | CUL4B | GRCh38.p7 | X:120566346 | TGTGTGTGTATAGGT[-/GT]ATATATATATATATA | 8450 |
rs59022882 | in-del | -/A | 0.00949095 | 0.0682305 | intron-variant | CUL4B | GRCh38.p7 | X:120556913 | CTGAAGTATATATAT[-/A]TTTTTTTTTTTTTTT | 8450 |
rs59133588 | snp | A/G | | | intron-variant | CUL4B | GRCh38.p7 | X:120565451 | CACTTTGGGAGGCCA[A/G]AGTGGGTGGATCACT | 8450 |
rs60058698 | in-del | -/ACAC | | | intron-variant | CUL4B | GRCh38.p7 | X:120543530 | CACACACACACACAC[-/ACAC]CCCTAATAATCGAAT | 8450 |
rs60471809 | in-del | -/ATATAT | | | intron-variant | CUL4B | GRCh38.p7 | X:120566390 | TATATATATATATAT[-/ATATAT]GTATATATATTTGGG | 8450 |
rs61390830 | in-del | -/ACACACAC | | | intron-variant | CUL4B | GRCh38.p7 | X:120543526 | CACACACACACACAC[-/ACACACAC]CCCTAATAATCGAAT | 8450 |
rs61752964 | snp | C/T | | | synonymous-codon | CUL4B | GRCh38.p7 | X:120535887 | CTGCCACTGAAGTTT[C/T]CTGCCACTATGTTTG | 8450 |
rs61752965 | snp | A/C/T | | | missense | CUL4B | GRCh38.p7 | X:120535891 | CACTGAAGTTTCCTG[A/C/T]CACTATGTTTGCCTA | 8450 |
rs61754550 | snp | A/G | 2.33926e-05 | 0.00341991 | missense | CUL4B | GRCh38.p7 | X:120544638 | AATAACTCCAGTCCC[A/G]TGTCCCTAAAATAAA | 8450 |
rs61757196 | snp | C/T | | | synonymous-codon | CUL4B | GRCh38.p7 | X:120547234 | AGAACAGAGATTTTC[C/T]ACAGCCTGCAAGGTT | 8450 |
rs61759504 | snp | A/G | | | missense, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120560385 | GCCACTGAAACCCCC[A/G]GGCAGAAGGACGAGG | 8450 |
rs62616188 | snp | A/G | 0.0142023 | 0.083063 | intron-variant | CUL4B | GRCh38.p7 | X:120566994 | ATGTGCCATGGCATG[A/G]GCCTATTTTTAACAT | 8450 |
rs62616189 | snp | C/T | 0.492017 | 0.0626724 | intron-variant | CUL4B | GRCh38.p7 | X:120567323 | GTAGAAATGGGGTTT[C/T]GCCATGTTGGCCAGG | 8450 |
rs62616190 | snp | C/T | 0.381341 | 0.212719 | intron-variant | CUL4B | GRCh38.p7 | X:120568269 | ATTTTGCTGACCTCA[C/T]AGTATTGCCTAGGGC | 8450 |
rs66749436 | in-del | -/A | | | intron-variant | CUL4B | GRCh38.p7 | X:120572483 | AAAAAAAAAAAAAAA[-/A]GAAAAAGAAAAGAAA | 8450 |
rs67116649 | in-del | -/TA | | | intron-variant | CUL4B | GRCh38.p7 | X:120556904 | TATTGTACTCTGAAG[-/TA]TATATATATTTTTTT | 8450 |
rs71820203 | in-del | -/A | | | intron-variant | CUL4B | GRCh38.p7 | X:120535705 | TGAGACTCTGTCTCA[-/A]AAAAAAAAAAAAAAA | 8450 |
rs71840531 | in-del | -/TA | 0.145386 | 0.227059 | intron-variant | CUL4B | GRCh38.p7 | X:120543701 | ACGACAGTTTAAGAC[-/TA]TTAAATTCAGCATGT | 8450 |
rs72098040 | in-del | -/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120556914 | TGAAGTATATATATA[-/T]TTTTTTTTTTTTTTG | 8450 |
rs72483160 | in-del | -/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120567141 | TTTTTTTTTTTTTTT[-/T]GAGACAGAGTTTGGC | 8450 |
rs73219157 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | CUL4B | GRCh38.p7 | X:120533301 | TTGATCCTTCCAGTT[A/G]CCCTGTAGATTGATT | 8450 |
rs73219159 | snp | A/G/T | 0.0550819 | 0.156547 | intron-variant | CUL4B | GRCh38.p7 | X:120546249 | GAGTGGGAGGGGGGC[A/G/T]AGGGATAAAAGACTA | 8450 |
rs73620006 | snp | C/G | 0.0131573 | 0.0800346 | intron-variant | CUL4B | GRCh38.p7 | X:120550648 | TGGAGGGTGGTTTAA[C/G]AACTTTAAGGCAAGA | 8450 |
rs73639317 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120540945 | TTATTAGAAGCCTCT[A/G]GGATCTTTTCCTTAT | 8450 |
rs73639318 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120549647 | CAGGAAACAGCAGGC[C/T]AATTAGATTGAGCAG | 8450 |
rs73639319 | snp | A/G | 0.0772873 | 0.180749 | intron-variant | CUL4B | GRCh38.p7 | X:120554758 | CTTTTGTATAACTAC[A/G]TATTTCCACATTATT | 8450 |
rs74700846 | snp | C/T | 0.5 | 0 | intron-variant | CUL4B | GRCh38.p7 | X:120541333 | GGTGAAACCCCGTCT[C/T]TACTAAAAATACAAA | 8450 |
rs75843245 | snp | A/G | 0.5 | 0 | intron-variant | CUL4B | GRCh38.p7 | X:120549263 | AATCAGCAAATGAAA[A/G]GAAAGCTTGGCAGAG | 8450 |
rs75966720 | snp | A/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120569234 | GAACCCTGCCGGCAG[A/T]CCCATCATGTTCTAC | 8450 |
rs76254851 | in-del | -/T/TT | 0.529357 | 0.0793548 | intron-variant | CUL4B | GRCh38.p7 | X:120529942 | AAAGTTTTTTTTTTT[-/T/TT]GGAAATCATATGCAT | 8450 |
rs77682015 | snp | A/G | 0.5 | 0 | intron-variant | CUL4B | GRCh38.p7 | X:120546035 | ATAATCATCAAGAGA[A/G]AAAAAAAAATAAGAG | 8450 |
rs78810044 | snp | G/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120546105 | ACATTTTTGGTAAGT[G/T]TGACAAAAATAAAAA | 8450 |
rs79448556 | snp | A/T | 0 | 0 | intron-variant | CUL4B | GRCh38.p7 | X:120556913 | CTGAAGTATATATAT[A/T]TTTTTTTTTTTTTTT | 8450 |
rs80123791 | snp | C/T | 0.5 | 0 | intron-variant | CUL4B | GRCh38.p7 | X:120574889 | ATTTGTTAAGATTCT[C/T]TTAAATTGGAAGCCT | 8450 |
rs111274026 | snp | C/G | | | intron-variant | CUL4B | GRCh38.p7 | X:120567360 | TTGAACTCCTGACCT[C/G]AGGTGATCCGCCCAC | 8450 |
rs111294164 | snp | C/T | 0.5 | 0 | intron-variant | CUL4B | GRCh38.p7 | X:120545567 | TGTATGTTGTGAAGC[C/T]GAAATATTTGCTTTC | 8450 |
rs111328778 | snp | G/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120572764 | GATCTACCTCACTAT[G/T]TTTAAGGGCAACATA | 8450 |
rs111414969 | snp | C/T | 0 | 0 | intron-variant | CUL4B | GRCh38.p7 | X:120532327 | AAAATATTAATGGTA[C/T]TGGCAGTATTACAGG | 8450 |
rs111463977 | snp | C/G | 0.5 | 0 | intron-variant | CUL4B | GRCh38.p7 | X:120545078 | TAGGTACATGGGAGG[C/G]GGAAGAGTTCATGAT | 8450 |
rs111551052 | snp | A/G | 0 | 0 | intron-variant, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120557710 | AATTTCTTATCAGGA[A/G]GGTCAAATATAAGCA | 8450 |
rs111604949 | snp | A/C | | | intron-variant | CUL4B | GRCh38.p7 | X:120549542 | TGTGAGACTCTGTCT[A/C]GAGAAGAGAAGAAAA | 8450 |
rs111777764 | snp | G/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120572763 | AGATCTACCTCACTA[G/T]TTTTAAGGGCAACAT | 8450 |
rs111794840 | snp | C/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120572651 | AACGTGCAGTTTTTG[C/T]TTTTTTTAAAAAAAG | 8450 |
rs111897905 | snp | C/T | 0.5 | 0 | intron-variant | CUL4B | GRCh38.p7 | X:120538410 | TAGTAACCTTATCTA[C/T]TATTTAGGTATAAAA | 8450 |
rs112085497 | snp | A/C/T | 7.62273e-05 | 0.00617315 | intron-variant | CUL4B | GRCh38.p7 | X:120547124 | CACGATTTTTTGTTT[A/C/T]AAAAAGGATATTCTC | 8450 |
rs112174090 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120533834 | GCACTTTGGTAGGCC[A/G]AGGCAGGCGGATCAC | 8450 |
rs112179164 | snp | A/G | | | intron-variant | CUL4B | GRCh38.p7 | X:120573165 | TACATATATACTTGT[A/G]TATATACAAATAGGA | 8450 |
rs112199597 | snp | A/C | 0.097024 | 0.197733 | intron-variant | CUL4B | GRCh38.p7 | X:120566897 | GTGGGGAGCCAGAGC[A/C]GCCACAGATGACTTC | 8450 |
rs112225382 | snp | C/T | 0 | 0 | intron-variant | CUL4B | GRCh38.p7 | X:120545332 | AAGGAAAGTCTAGAA[C/T]CAAATGTGAATTTTT | 8450 |
rs112294904 | snp | A/G | 0.113033 | 0.209141 | intron-variant | CUL4B | GRCh38.p7 | X:120535431 | TTAAACTGGCCAGAT[A/G]CGGTGGTTCACACCT | 8450 |
rs112347202 | snp | A/C | | | intron-variant | CUL4B | GRCh38.p7 | X:120565878 | CTACAGGCGCCTACC[A/C]CCACGCCCAGCTAAT | 8450 |
rs112414111 | snp | C/T | 0.256758 | 0.249909 | intron-variant | CUL4B | GRCh38.p7 | X:120574206 | CAAGCTTCCTAGACA[C/T]GTTGTTAACAATATT | 8450 |
rs112435073 | snp | C/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120527073 | GATTCTTTTTTTTTT[C/T]TTTTGAGACGGAGTC | 8450 |
rs112463857 | snp | A/G | 0.00211696 | 0.0324653 | intron-variant | CUL4B | GRCh38.p7 | X:120548419 | AAAATTTACTTAAAC[A/G]TTCTTGGATTTTCCT | 8450 |
rs112641571 | snp | A/C | 0.0879364 | 0.190356 | intron-variant | CUL4B | GRCh38.p7 | X:120544733 | ACATGTTCCCATGCT[A/C]ATTAGGGCTCCAGGG | 8450 |
rs112685907 | snp | C/T | 0 | 0 | intron-variant | CUL4B | GRCh38.p7 | X:120542664 | TGCCCAGGCTGACCT[C/T]AAACTCCTGGGCTGA | 8450 |
rs112775410 | snp | C/G | 0.00158814 | 0.0281345 | intron-variant, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120558840 | AAAAATCTCTGAAAC[C/G]AATTTGAAAATGCAA | 8450 |
rs112799744 | snp | C/G | 0.139144 | 0.224078 | intron-variant | CUL4B | GRCh38.p7 | X:120548001 | CTTGTGATCGTGTAA[C/G]TTAACACTTAATAAA | 8450 |
rs112906706 | snp | G/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120545105 | TGATACTATTCTATT[G/T]TCGTGTATACATGGA | 8450 |
rs113073926 | snp | A/G | 0.113499 | 0.209446 | intron-variant | CUL4B | GRCh38.p7 | X:120531923 | GCCTTTCCGGAACAC[A/G]ATATGACATTATGTA | 8450 |
rs113213082 | snp | C/T | 0.0456269 | 0.143985 | intron-variant, missense | CUL4B | GRCh38.p7 | X:120559782 | CAAATTTCTCACCTG[C/T]AAAATCCGGATCAAT | 8450 |
rs113251042 | snp | C/T | 0.00844089 | 0.0644143 | intron-variant | CUL4B | GRCh38.p7 | X:120535475 | TTTAGGAGGCCGAGG[C/T]GCGTGGATCACAAGG | 8450 |
rs113321588 | in-del | -/A | 0 | 0 | intron-variant | CUL4B | GRCh38.p7 | X:120536777 | GAGGCGGGGGGGATC[-/A]CTTGAGCCCAAGAGT | 8450 |
rs113467361 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120534383 | AAAAAAAAAACTCAA[A/G]ACAGTTCTGAGGCAA | 8450 |
rs113484736 | snp | C/T | 0 | 0 | intron-variant | CUL4B | GRCh38.p7 | X:120540903 | AGTAAGCAATGATCA[C/T]TGGGCATATGATATC | 8450 |
rs113530931 | snp | A/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120528352 | GTGGAGGTTGTAGTG[A/T]AACGTGATCGCGCCA | 8450 |
rs113536773 | snp | G/T | 0.0026455 | 0.0362733 | intron-variant | CUL4B | GRCh38.p7 | X:120574343 | AGCCTCCTGAGTAGC[G/T]GGGACTACAGGCGCC | 8450 |
rs113566433 | snp | C/T | 0.5 | 0 | synonymous-codon | CUL4B | GRCh38.p7 | X:120546610 | AAGAACGCTATCCAA[C/T]GAATCCCTGAAACAT | 8450 |
rs113751799 | snp | C/T | 0.0271702 | 0.113344 | intron-variant | CUL4B | GRCh38.p7 | X:120552126 | ACATATTATGCATTA[C/T]GTATTTATTATTTAC | 8450 |
rs113866666 | snp | A/G | 0.5 | 0 | intron-variant | CUL4B | GRCh38.p7 | X:120535413 | CAATTATAAAACAAC[A/G]GCTTAAACTGGCCAG | 8450 |
rs113876547 | snp | A/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120531332 | CCTCAAAAAAAAAAT[A/T]TTTTTTTTTTCAAAT | 8450 |
rs113902030 | snp | A/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120542207 | TAAATATACATTATA[A/T]ATACCTCATATATGT | 8450 |
rs114378992 | snp | A/C | 0.00158814 | 0.0281345 | intron-variant | CUL4B | GRCh38.p7 | X:120554451 | TTAATCACTGCCTCA[A/C]ACCCACAGGATCTCA | 8450 |
rs116331606 | snp | C/T | 0.097024 | 0.197733 | upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120577252 | CTGAATTTCAGGGGA[C/T]GTGACTTGATTATGA | 8450 |
rs121434615 | snp | C/T | | | missense | CUL4B | GRCh38.p7 | X:120539349 | GTAGATTCAAAACTT[C/T]GTGCAGGCAACAAAG | 8450 |
rs121434616 | snp | C/T | | | stop-gained | CUL4B | GRCh38.p7 | X:120544179 | GATTCTTTTGAACAA[C/T]GATTTTTGGAAGAAA | 8450 |
rs137964422 | snp | C/T | 0.00844089 | 0.0644143 | intron-variant, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120557653 | TGCTATAGGATTACA[C/T]TATAGGTAGAACTTC | 8450 |
rs138049865 | snp | A/C | 0.00528398 | 0.051128 | intron-variant | CUL4B | GRCh38.p7 | X:120554040 | TTTATCAGACAGCTG[A/C]TCTGGCCCAGTGTAG | 8450 |
rs138091083 | snp | A/G | 0.0209675 | 0.10022 | intron-variant | CUL4B | GRCh38.p7 | X:120549409 | ATACAAAAATTAGCC[A/G]GGTGTGGTGGTGTGC | 8450 |
rs138110657 | snp | A/T | 0.0874553 | 0.189945 | intron-variant | CUL4B | GRCh38.p7 | X:120534190 | GGCTAAGCAACATAG[A/T]GAGACCCTGTCTCTA | 8450 |
rs138140079 | snp | A/G | 0.00211696 | 0.0324653 | downstream-variant-500B | CUL4B | GRCh38.p7 | X:120524104 | ACACTCACATACACA[A/G]CAAAAATTTCAAGAG | 8450 |
rs138353119 | snp | C/T | 0.00528398 | 0.051128 | intron-variant | CUL4B | GRCh38.p7 | X:120542220 | TAAATACCTCATATA[C/T]GTAGTAGCCATATTA | 8450 |
rs138458541 | snp | A/C | 0.0126344 | 0.0784702 | intron-variant | CUL4B | GRCh38.p7 | X:120573197 | GCTTTAGTATTTTTT[A/C]AAATGGCATAATTAC | 8450 |
rs138604687 | snp | G/T | 0.00105904 | 0.0229869 | intron-variant | CUL4B | GRCh38.p7 | X:120543313 | ACCTTGCTGTAGTCG[G/T]CTTTTTCCAAGTTTT | 8450 |
rs138631097 | snp | G/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120545873 | TTGGCAGGGGGTGGG[G/T]GTGGGGAGGGGTGAT | 8450 |
rs138702339 | snp | C/T | 0.00633741 | 0.0559334 | intron-variant | CUL4B | GRCh38.p7 | X:120568905 | GCCATAAAATAGTCT[C/T]AAGTAGTAGACATGT | 8450 |
rs138733508 | snp | A/G | 0.0276852 | 0.114351 | intron-variant | CUL4B | GRCh38.p7 | X:120533169 | TTCATCCTCAACATA[A/G]TAGCTAGCCGCTGCT | 8450 |
rs139093029 | snp | A/C | 2.28718e-05 | 0.00338162 | intron-variant | CUL4B | GRCh38.p7 | X:120543705 | CAGTTTAAGACTATT[A/C]AATTCAGCATGTGGT | 8450 |
rs139132647 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120535385 | CACTGTCATCATGCG[G/T]ATATCTAGGATACAA | 8450 |
rs139239689 | snp | C/T | 0.000342332 | 0.0130786 | synonymous-codon | CUL4B | GRCh38.p7 | X:120544123 | AAATACCTCTCTTTC[C/T]TGCATTAATTTTTGG | 8450 |
rs139252360 | snp | C/T | 0.00633741 | 0.0559334 | intron-variant | CUL4B | GRCh38.p7 | X:120570101 | AGCACCAAATCTTAC[C/T]CAAATACCCTACTTG | 8450 |
rs139622722 | snp | A/T | 0.0261392 | 0.111294 | intron-variant | CUL4B | GRCh38.p7 | X:120528248 | CCCATCTGTACTAAA[A/T]ATACAAGAATTAGCC | 8450 |
rs139699873 | snp | A/G | 0.00791544 | 0.0624105 | intron-variant | CUL4B | GRCh38.p7 | X:120527348 | CAGGGATGAGCCACC[A/G]TGCCCAGGTATGTTG | 8450 |
rs139827867 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | CUL4B | GRCh38.p7 | X:120549941 | ACATTGTGCACTTCC[A/G]GTACTTCTCTAAGTC | 8450 |
rs140061107 | snp | A/G | 0.0115877 | 0.0752302 | intron-variant | CUL4B | GRCh38.p7 | X:120570515 | TCTAAAATAGTTCCT[A/G]CTAGTTCCTTAACAG | 8450 |
rs140116576 | snp | C/T | 0.000529661 | 0.016265 | intron-variant, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120558413 | AAAGTACTGTCTATG[C/T]GCAAGGTACTTTATA | 8450 |
rs140159218 | snp | C/T | 0.0068637 | 0.0581785 | intron-variant | CUL4B | GRCh38.p7 | X:120551472 | TCCCAAAGTGCTGGA[C/T]TACATGCATGAGCCA | 8450 |
rs140279360 | snp | A/G | 0.0214859 | 0.101397 | intron-variant | CUL4B | GRCh38.p7 | X:120528550 | ATATGGTAAAACCCC[A/G]TCTCTACTAAAAACA | 8450 |
rs140377755 | snp | A/G | 0.00211696 | 0.0324653 | intron-variant | CUL4B | GRCh38.p7 | X:120567993 | AAGCACTTGTATTCC[A/G]TTTAATGCCTGAAAT | 8450 |
rs140582079 | snp | A/G | 0.00158814 | 0.0281345 | upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120576576 | AGAACCAACTAGATC[A/G]AGGGACTCAAATGGT | 8450 |
rs140908460 | snp | A/G | 0.00370173 | 0.0428621 | intron-variant | CUL4B | GRCh38.p7 | X:120536852 | TTTTTCTAAGTATCT[A/G]TTTTTAAATGACAAG | 8450 |
rs141053217 | snp | C/G | 0.0831127 | 0.186141 | upstream-variant-2KB, intron-variant | CUL4B | GRCh38.p7 | X:120563045 | CACTTGTTTTTGTGT[C/G]TTGAAAAGTCCCTGA | 8450 |
rs141093192 | snp | A/C | 0.0100156 | 0.0700533 | intron-variant | CUL4B | GRCh38.p7 | X:120554416 | AGCACGCAAACAAAC[A/C]AAACAGTCAAATGAA | 8450 |
rs141125777 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | CUL4B | GRCh38.p7 | X:120556313 | ATTTGAGTATTTTGC[A/G]TGTACTAATTTTCAC | 8450 |
rs141209231 | snp | C/T | 0.00738971 | 0.0603345 | intron-variant | CUL4B | GRCh38.p7 | X:120572333 | AGCCGGGTGTGGTGG[C/T]GCATGCCTATAATCC | 8450 |
rs141353300 | snp | A/C/G | 4.56181e-05 | 0.0047757 | synonymous-codon, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120560273 | AGATGAGGAGGAGGA[A/C/G]GAGGAGGATTCCTCA | 8450 |
rs142005526 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120568584 | CATTCAACAAAAATA[C/T]ATTGAGCAAATACTC | 8450 |
rs142029145 | snp | C/T | 0.0126344 | 0.0784702 | intron-variant | CUL4B | GRCh38.p7 | X:120574828 | TGCTATTCTTTTACT[C/T]GTTTTTTTCTTCTGT | 8450 |
rs142211300 | snp | A/G | 4.93267e-05 | 0.00496598 | synonymous-codon | CUL4B | GRCh38.p7 | X:120539287 | GATAAATCTAAATAT[A/G]ATCATAATTTTATCC | 8450 |
rs142230816 | snp | C/T | 0.0131573 | 0.0800346 | intron-variant | CUL4B | GRCh38.p7 | X:120534975 | AGATTAGATATTGCA[C/T]ACTGTTTCCCTTAAC | 8450 |
rs142286481 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120571734 | GTGATGGTCCATTTA[C/T]ACACATATTTTTTCA | 8450 |
rs142381957 | snp | C/T | 0.0235569 | 0.105941 | intron-variant | CUL4B | GRCh38.p7 | X:120550702 | TTTTGAGGTCAAGTT[C/T]GGAGGGAACATTCTG | 8450 |
rs142680078 | snp | A/G | 0.0173306 | 0.0914601 | intron-variant | CUL4B | GRCh38.p7 | X:120549492 | AGGTTGCAGTGAGCC[A/G]AGAATGTGCCATTGC | 8450 |
rs142684736 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120571466 | AAATTACTCAAGGGC[A/G]GGGGATGCACCCTCC | 8450 |
rs142761265 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120568946 | CGTTCAGAGCCCCAC[C/T]CACCAAGAGAAAAAA | 8450 |
rs143082577 | snp | A/C | 0.0126344 | 0.0784702 | intron-variant | CUL4B | GRCh38.p7 | X:120573606 | CCCCATATCCTTAGC[A/C]ACACTAAATTTTATC | 8450 |
rs143093777 | snp | A/C | 0.00370173 | 0.0428621 | intron-variant | CUL4B | GRCh38.p7 | X:120533448 | TAATTTTTTAACTCA[A/C]TATTCTATGTTACAA | 8450 |
rs143306049 | snp | A/G | 0.00422943 | 0.0457911 | intron-variant | CUL4B | GRCh38.p7 | X:120548536 | AGAATAGTTAAATAT[A/G]GATTTTAAAATCTGT | 8450 |
rs143339072 | snp | C/G | 0.00317376 | 0.039709 | intron-variant | CUL4B | GRCh38.p7 | X:120567712 | AGCGAGACCCTGTCT[C/G]TATCGAAAAAAAAAA | 8450 |
rs143407679 | snp | C/T | 0.00422943 | 0.0457911 | intron-variant | CUL4B | GRCh38.p7 | X:120539121 | GACAATCAGGTAACA[C/T]TCCTCACGTATCCCC | 8450 |
rs143430595 | snp | A/C | 0.00738971 | 0.0603345 | upstream-variant-2KB, intron-variant | CUL4B | GRCh38.p7 | X:120563206 | TGGAAGCACTCCTAT[A/C]TGTTTTGAATATACC | 8450 |
rs143533281 | snp | A/G | 0.0126344 | 0.0784702 | intron-variant | CUL4B | GRCh38.p7 | X:120553985 | TATTTTTTCAATTTC[A/G]CTAATGGTGTCTACT | 8450 |
rs143580749 | snp | C/T | 0.00248554 | 0.0351652 | synonymous-codon | CUL4B | GRCh38.p7 | X:120526815 | TCTTTCCATGTAGTC[C/T]CGGTCAATTAAAGAT | 8450 |
rs143725877 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120570545 | GAAAAAAAAATTGCC[A/G]GTCCTTGCATTTGAA | 8450 |
rs143768157 | snp | A/G | 0.0312828 | 0.12109 | intron-variant | CUL4B | GRCh38.p7 | X:120573159 | TTTATGTACATATAT[A/G]CTTGTATATATACAA | 8450 |
rs143921252 | snp | C/T | 0.0426578 | 0.139675 | intron-variant | CUL4B | GRCh38.p7 | X:120542951 | GCAATCTCTTATTTA[C/T]AAATTGCCAATTACC | 8450 |
rs143946589 | snp | C/T | 0.00896606 | 0.0663524 | intron-variant | CUL4B | GRCh38.p7 | X:120564498 | GTAATCCCAACTACT[C/T]GGGAGGATAAGGCAG | 8450 |
rs144046487 | snp | A/G | 0.0147244 | 0.0845304 | intron-variant | CUL4B | GRCh38.p7 | X:120534723 | GCAAAGCCACTTGAC[A/G]TGGTAATACAGTATT | 8450 |
rs144057361 | snp | C/T | 0.00633741 | 0.0559334 | intron-variant | CUL4B | GRCh38.p7 | X:120529485 | AACTCTATCAATGTT[C/T]ATCATCCAAGGGTTT | 8450 |
rs144312827 | snp | A/G | 4.61649e-05 | 0.0048042 | synonymous-codon | CUL4B | GRCh38.p7 | X:120544610 | TTTCTGATCACTTAT[A/G]ATATGAGCCCTAAAT | 8450 |
rs144326802 | snp | A/G | 0.0152462 | 0.0859689 | upstream-variant-2KB, intron-variant | CUL4B | GRCh38.p7 | X:120562048 | AAGTGTGTATTCTAA[A/G]GCGAAGAAATGGAAA | 8450 |
rs144359681 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | CUL4B | GRCh38.p7 | X:120537323 | CGTTATAGGATCTCT[C/T]CTCCATTCTTTTCCC | 8450 |
rs144519604 | snp | A/G | | | intron-variant | CUL4B | GRCh38.p7 | X:120550417 | AAAACGTGTAATTAC[A/G]ATTGAGTGTGCTAGA | 8450 |
rs144648119 | snp | A/C/G | 0.00399815 | 0.0445326 | intron-variant | CUL4B | GRCh38.p7 | X:120543680 | TAAAGTGCTGCAAGT[A/C/G]ATTTAACGACAGTTT | 8450 |
rs144667410 | snp | A/T | 0.00633741 | 0.0559334 | intron-variant | CUL4B | GRCh38.p7 | X:120566833 | CATCTGGAAAGCAGA[A/T]TTAAGGACTAAAAGT | 8450 |
rs145134351 | snp | C/T | 4.94419e-05 | 0.00497177 | missense, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120560500 | TACTGTTACTGCTGC[C/T]ACTGCTGCTGCTGTT | 8450 |
rs145291707 | snp | C/T | 0.00211696 | 0.0324653 | intron-variant | CUL4B | GRCh38.p7 | X:120527450 | AGGGTCTTGCTATGT[C/T]GCCCAGGCTGACCTT | 8450 |
rs145361675 | snp | G/T | 0.0068637 | 0.0581785 | intron-variant | CUL4B | GRCh38.p7 | X:120537392 | GTGGCTTAAACACCT[G/T]GCAGCAACCCCCATT | 8450 |
rs145734746 | snp | C/T | 0.0126344 | 0.0784702 | intron-variant | CUL4B | GRCh38.p7 | X:120571751 | CACATATTTTTTCAA[C/T]AAATACAGTCGGCCC | 8450 |
rs145738307 | snp | A/G | 0.00949095 | 0.0682305 | intron-variant | CUL4B | GRCh38.p7 | X:120552704 | AAAATATATATAAAC[A/G]TGTAGCAAATGACAT | 8450 |
rs145773709 | snp | A/T | 0.00949095 | 0.0682305 | intron-variant | CUL4B | GRCh38.p7 | X:120568875 | CCCATAGTTTACAAT[A/T]TCGTAAGGAGACTTG | 8450 |
rs145808703 | snp | C/T | 0.00104793 | 0.0228663 | missense | CUL4B | GRCh38.p7 | X:120574553 | TTCATTTACTCACCA[C/T]CGTCTTTAGAGGTAG | 8450 |
rs145841074 | snp | A/G | 0.00211696 | 0.0324653 | intron-variant | CUL4B | GRCh38.p7 | X:120546875 | TTCCCTTAGGAGATT[A/G]TTTTTCCTCAAGTGG | 8450 |
rs145931683 | snp | A/G | 0.00844089 | 0.0644143 | intron-variant | CUL4B | GRCh38.p7 | X:120549753 | CTTAAGGGAATTTAC[A/G]TTTATTTCATGTGCC | 8450 |
rs146064671 | snp | A/G | 0.00422943 | 0.0457911 | intron-variant | CUL4B | GRCh38.p7 | X:120570476 | GCCATACGGTCTCTG[A/G]CAAAACTCTAAACTC | 8450 |
rs146481846 | snp | C/T | 0.0425 | 0.139441 | upstream-variant-2KB, intron-variant | CUL4B | GRCh38.p7 | X:120562413 | ACACAATATCAAAAA[C/T]TAAATTTGCCAACCT | 8450 |
rs146563437 | snp | A/G | 0.0168099 | 0.0901243 | intron-variant | CUL4B | GRCh38.p7 | X:120567273 | GGATTACAGGTGTGC[A/G]CCACCATGCCCAGCT | 8450 |
rs147026736 | snp | C/T | 0.0126344 | 0.0784702 | intron-variant | CUL4B | GRCh38.p7 | X:120547663 | GGTTACTACTGAGTG[C/T]CAACTTGATTGGATT | 8450 |
rs147036781 | snp | C/T | 0.0276852 | 0.114351 | intron-variant | CUL4B | GRCh38.p7 | X:120542012 | GGCAGGAGGATCAAT[C/T]GAAGCCAGGAGGTCA | 8450 |
rs147176324 | snp | A/G | 0.00317376 | 0.039709 | intron-variant | CUL4B | GRCh38.p7 | X:120564160 | ATACAAAAATGAGCC[A/G]GACATGGTGGTGTTC | 8450 |
rs147191224 | snp | A/G | 0.000189982 | 0.00974449 | synonymous-codon | CUL4B | GRCh38.p7 | X:120532509 | CTTGTCACCATCTTC[A/G]ATGTCTTTGCCCTTT | 8450 |
rs147302377 | snp | A/G | 0.00633741 | 0.0559334 | intron-variant | CUL4B | GRCh38.p7 | X:120565930 | AGATGAGGTTTCACT[A/G]TGTTAGCCAGGATGG | 8450 |
rs147339235 | snp | C/G | 0.0173306 | 0.0914601 | intron-variant, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120559306 | AATTCAGCTCAAATA[C/G]ATTTTTAAAAATTGC | 8450 |
rs147493910 | snp | A/C | 0.0261392 | 0.111294 | intron-variant | CUL4B | GRCh38.p7 | X:120534052 | GCCTGGGTGACAGAG[A/C]AAGATTCCGTCTTGA | 8450 |
rs147503620 | snp | C/T | 0.0147244 | 0.0845304 | intron-variant, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120557770 | GTTTATGTGAGAATA[C/T]GTGGTCTAATTATAG | 8450 |
rs147767603 | snp | C/T | 0.0317957 | 0.122012 | upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120576927 | GGACTATTGTGATTG[C/T]CTGTCCTACCAGGAC | 8450 |
rs147777719 | snp | C/T | 0.00633741 | 0.0559334 | intron-variant | CUL4B | GRCh38.p7 | X:120572012 | AGGCCTGTGGAGGAA[C/T]GATGAGAGATGAAGA | 8450 |
rs147934039 | snp | G/T | 0.00422943 | 0.0457911 | intron-variant | CUL4B | GRCh38.p7 | X:120551465 | CTCAGCCTCCCAAAG[G/T]GCTGGATTACATGCA | 8450 |
rs147988164 | snp | C/T | 0.0115877 | 0.0752302 | upstream-variant-2KB, intron-variant | CUL4B | GRCh38.p7 | X:120563391 | AGGCATGTATCACTA[C/T]GCCTGCTAATTTTTT | 8450 |
rs148154758 | snp | A/G | 0.0126344 | 0.0784702 | intron-variant | CUL4B | GRCh38.p7 | X:120530955 | CATGGTAATCCTTTA[A/G]GAAAATATCCTGTCT | 8450 |
rs148244845 | snp | A/G | 0.0772873 | 0.180749 | intron-variant | CUL4B | GRCh38.p7 | X:120548653 | AGCCTGGCCAACATA[A/G]TGAAACCCCGTCTCC | 8450 |
rs148314701 | snp | C/T | 0.00422943 | 0.0457911 | utr-variant-3-prime | CUL4B | GRCh38.p7 | X:120526034 | TTTCTACTTTAGCTA[C/T]TTTTATAAGTACTTG | 8450 |
rs148358426 | snp | C/T | 0.0131573 | 0.0800346 | intron-variant | CUL4B | GRCh38.p7 | X:120569279 | AAGACAACCCTTGCC[C/T]TCCATTCTCAATTGG | 8450 |
rs148517066 | snp | A/G | 0.00211696 | 0.0324653 | intron-variant | CUL4B | GRCh38.p7 | X:120566857 | TAAAAGTTAGAGATA[A/G]GCTGTTTTCCCTGAG | 8450 |
rs148681084 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120534949 | TAGTCATGAAAAGCT[A/G]AAGTTTTTTGAGATT | 8450 |
rs148700620 | snp | A/G | 0.00418379 | 0.0455455 | synonymous-codon | CUL4B | GRCh38.p7 | X:120538205 | GGTGAAAGCAGCTCC[A/G]CATTCTATTAAAGAT | 8450 |
rs148842414 | snp | A/G | 0.017851 | 0.0927731 | intron-variant | CUL4B | GRCh38.p7 | X:120529219 | AGGGTGGTAATGAGG[A/G]GTGCGATATTAGGTT | 8450 |
rs149016283 | snp | C/T | 0.000387367 | 0.0139116 | missense | CUL4B | GRCh38.p7 | X:120574592 | TCATCATTCCCATCT[C/T]CTGATCCAGATGACT | 8450 |
rs149267293 | snp | A/G | 0.018891 | 0.0953342 | intron-variant | CUL4B | GRCh38.p7 | X:120550385 | GAAAGGGCTTCTAGT[A/G]TGAGAAAAGTTGCCA | 8450 |
rs149574322 | snp | A/G | 0.00158814 | 0.0281345 | downstream-variant-500B | CUL4B | GRCh38.p7 | X:120524123 | AAATTTCAAGAGTAT[A/G]GCTAGACATCATATT | 8450 |
rs149655449 | snp | C/G | 0.01368 | 0.0815649 | intron-variant | CUL4B | GRCh38.p7 | X:120528383 | CTGCACTCCAACCTG[C/G]GTGACAGAGCAAGAA | 8450 |
rs149798485 | snp | A/G | 0.0199298 | 0.0978146 | intron-variant | CUL4B | GRCh38.p7 | X:120552282 | CCTTCCCAGTAGCTC[A/G]GATTACAGACACGTG | 8450 |
rs150132567 | snp | G/T | 0.00633741 | 0.0559334 | intron-variant | CUL4B | GRCh38.p7 | X:120543180 | ATTTATTGGTGCTCA[G/T]AGTTACTATACTTTA | 8450 |
rs150332939 | snp | A/G | 0.0317957 | 0.122012 | intron-variant | CUL4B | GRCh38.p7 | X:120572397 | TTGAACCCAGGAGAC[A/G]GAGGTTGCAGTGAGC | 8450 |
rs150351316 | snp | A/G | 0.0100156 | 0.0700533 | intron-variant | CUL4B | GRCh38.p7 | X:120549032 | AAATTTAAAACAACA[A/G]GCATGCTAAAACTCT | 8450 |
rs150721026 | snp | A/G | 0.0768 | 0.180282 | intron-variant | CUL4B | GRCh38.p7 | X:120556989 | CAATCTCGGCTCACC[A/G]CAACCTCTACCTCCT | 8450 |
rs150915713 | snp | C/G | 0.0440191 | 0.141675 | intron-variant | CUL4B | GRCh38.p7 | X:120569424 | GGAGTGCAGTGGTGC[C/G]ATCTTGGCTCACTGC | 8450 |
rs150997041 | snp | C/G | 0.00528398 | 0.051128 | intron-variant | CUL4B | GRCh38.p7 | X:120571624 | ATTACTTGAAAAGGG[C/G]AACAGTGTGTGCAAA | 8450 |
rs151201128 | snp | A/G | 0.0131573 | 0.0800346 | intron-variant | CUL4B | GRCh38.p7 | X:120567816 | GGAGTTCCAGCTGCA[A/G]TGAGCTATGATGGTG | 8450 |
rs151245556 | snp | C/T | 0.00475684 | 0.0485365 | intron-variant | CUL4B | GRCh38.p7 | X:120539826 | AAAATTTGCTACATG[C/T]TTACGGATACATAGT | 8450 |
rs151254898 | snp | A/G | 0.000377928 | 0.0137412 | missense | CUL4B | GRCh38.p7 | X:120543794 | GTTTGTTAACATGAT[A/G]TAGATATTCAGGAAC | 8450 |
rs180820384 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120572837 | CTAATTATCACACGT[G/T]ATTGTTGTTGCTTTT | 8450 |
rs180826807 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120555352 | TAAATATGCTGTATA[C/G]CAGCATATCCAAATA | 8450 |
rs180959877 | snp | C/T | 0.00105904 | 0.0229869 | upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120577095 | GTTACATTTCTTGGA[C/T]TCTCAATGTGTATAA | 8450 |
rs180965104 | snp | A/C | 0.00370173 | 0.0428621 | intron-variant | CUL4B | GRCh38.p7 | X:120534345 | GGGTGACAGAGTGAG[A/C]CCCTGTCTCATTAAA | 8450 |
rs180977347 | snp | A/C | 0.0126344 | 0.0784702 | intron-variant, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120557623 | CATGTCACCAGAAAT[A/C]ATCTTTGGGATTCAT | 8450 |
rs180986112 | snp | A/C | 0.00105904 | 0.0229869 | intron-variant | CUL4B | GRCh38.p7 | X:120568824 | AAAGCACACAGACCT[A/C]AGTCCAGTTCTTCAC | 8450 |
rs180996085 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120542443 | CTTTTACCTATTTGC[A/G]GCATTCTCAAAGTAA | 8450 |
rs181026623 | snp | G/T | 0.00105904 | 0.0229869 | intron-variant | CUL4B | GRCh38.p7 | X:120550616 | CTTTACAGCACAGAG[G/T]CTCACCTGTGTTTGG | 8450 |
rs181089125 | snp | C/T | 0.0173306 | 0.0914601 | intron-variant | CUL4B | GRCh38.p7 | X:120537703 | ACATTTCAAAACTAC[C/T]TTCTACCTACATCTT | 8450 |
rs181090615 | snp | A/T | 0.00422943 | 0.0457911 | intron-variant | CUL4B | GRCh38.p7 | X:120554690 | GTTCTAAGCAGATAT[A/T]TGCCAGTAAGTGTTT | 8450 |
rs181139558 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120548138 | AATTAGCTGGGCCCA[C/G]TGGTGTGTACCTGTA | 8450 |
rs181147215 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | CUL4B | GRCh38.p7 | X:120565520 | TACCCTGTCTCTACT[A/G]AAAATACAAAAATTA | 8450 |
rs181163627 | snp | A/G | 0.00370173 | 0.0428621 | intron-variant | CUL4B | GRCh38.p7 | X:120572582 | TAAAACCAGCCCCCA[A/G]AGGTAACCTCAGTTA | 8450 |
rs181164324 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120530655 | CTATAAGGTGACTCT[C/G]TCTGATCTCTGACTC | 8450 |
rs181280879 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120550173 | TTGAGTCAACACTAT[C/T]TATCTCCCAACCACT | 8450 |
rs181283715 | snp | A/G | 0.000529661 | 0.016265 | utr-variant-3-prime | CUL4B | GRCh38.p7 | X:120526039 | ACTTTAGCTATTTTT[A/G]TAAGTACTTGTTAAT | 8450 |
rs181386008 | snp | C/T | 0.0026455 | 0.0362733 | intron-variant | CUL4B | GRCh38.p7 | X:120533698 | CTCTTACCACACTTA[C/T]AGTCAGTACCACAAG | 8450 |
rs181581551 | snp | A/C | 0.00158814 | 0.0281345 | intron-variant | CUL4B | GRCh38.p7 | X:120559663 | ACTATTGCTACCTGC[A/C]TTTCTAGGCATTGGA | 8450 |
rs181598882 | snp | A/C | 0.0869739 | 0.189532 | intron-variant | CUL4B | GRCh38.p7 | X:120543532 | CACACACACACACAC[A/C]CCCCTAATAATCGAA | 8450 |
rs181700085 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | CUL4B | GRCh38.p7 | X:120564764 | TAAAATACATTTTCA[A/G]GGTTGAACTCACGGG | 8450 |
rs181713732 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | CUL4B | GRCh38.p7 | X:120529010 | GAGGGGAAAAGAGGG[A/G]AAGTAGTCTGATACA | 8450 |
rs181713837 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120547629 | GATGCCAGGCTAGAA[C/T]AGCCTAGGCAACTGT | 8450 |
rs181824081 | snp | A/G/T | 0.0126344 | 0.0784702 | intron-variant | CUL4B | GRCh38.p7 | X:120572973 | TTTCAGTTCTGTTTA[A/G/T]TTATGCAAATGATAT | 8450 |
rs181874595 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120568335 | TAATCAAGTTTGACA[A/G]CTTATCTAAGCTGCC | 8450 |
rs181887874 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120538226 | TATTAAAGATGTTTG[C/T]ACATGTATAATATTT | 8450 |
rs181974679 | snp | C/T | 0.000529661 | 0.016265 | intron-variant, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120558901 | GCTACAAAATCCATA[C/T]ATTTTTAAGTGAAAT | 8450 |
rs181978416 | snp | A/C | 0.00581083 | 0.0535878 | utr-variant-3-prime | CUL4B | GRCh38.p7 | X:120524901 | CTCCTCCTAACAGGA[A/C]CAACTCTATCTAAAA | 8450 |
rs182138492 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120546812 | CTAAAAAACACCTTT[A/C]AAAACAAGTCTTAGA | 8450 |
rs182198427 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120530964 | CCTTTAAGAAAATAT[A/C]CTGTCTTTGATGTGT | 8450 |
rs182238767 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | CUL4B | GRCh38.p7 | X:120575345 | CCAGGTCCACCTTCA[A/G]TAAGTTCCTAAACAA | 8450 |
rs182252335 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | CUL4B | GRCh38.p7 | X:120556658 | CAGCCTGGGCAACAT[A/G]GCAAGACCCCTATCT | 8450 |
rs182256032 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | CUL4B | GRCh38.p7 | X:120542556 | TTAGTGTAAAAAGGA[A/G]TACCTTTCCTTACTG | 8450 |
rs182370361 | snp | A/G | 0.00370173 | 0.0428621 | intron-variant | CUL4B | GRCh38.p7 | X:120571047 | GGTGGGGTGGGGTGG[A/G]GGGAATAATTAATGT | 8450 |
rs182376520 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120552803 | GTCACTGGTCTAAGG[A/G]GTGGAGTCTTAGTTT | 8450 |
rs182378086 | snp | A/G | 0.00211696 | 0.0324653 | intron-variant | CUL4B | GRCh38.p7 | X:120535433 | AAACTGGCCAGATGC[A/G]GTGGTTCACACCTGT | 8450 |
rs182400362 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120564382 | AGGCTGAGGCGGGCC[A/G]ATCACCTGAGGTCAG | 8450 |
rs182421109 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120528320 | ACTGAGGCAGGAGAA[C/T]TGCTTGAACCCGGGA | 8450 |
rs182521266 | snp | A/C | | | intron-variant | CUL4B | GRCh38.p7 | X:120556199 | TGAAATGGGCTTATT[A/C]TTAAGTAATAGCTTA | 8450 |
rs182524611 | snp | A/C | 0.0168099 | 0.0901243 | intron-variant | CUL4B | GRCh38.p7 | X:120574086 | CCCCGCCAACCCCTC[A/C]TCCCCCATCACCTGC | 8450 |
rs182530263 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120539425 | GAATACACGAGGTAC[C/T]GGGCACTATATATAC | 8450 |
rs182560460 | snp | A/G | 0.00317376 | 0.039709 | intron-variant | CUL4B | GRCh38.p7 | X:120548705 | CGGACATGGTGGTGC[A/G]CGCCTGTAATCCCAG | 8450 |
rs182690643 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | CUL4B | GRCh38.p7 | X:120545321 | AAACTGCTACAAAGG[A/G]AAGTCTAGAACCAAA | 8450 |
rs182805889 | snp | A/G | 0.0115877 | 0.0752302 | intron-variant | CUL4B | GRCh38.p7 | X:120565910 | TTTTTTTGTATTTTT[A/G]GTAGAGATGAGGTTT | 8450 |
rs182821660 | snp | C/G | 0.0026455 | 0.0362733 | intron-variant | CUL4B | GRCh38.p7 | X:120540311 | TAAAAATTTCAGATT[C/G]AGATTTTATGACTCA | 8450 |
rs182960631 | snp | A/G | 0.00738971 | 0.0603345 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | CUL4B | GRCh38.p7 | X:120561453 | GAGTGGGGGGGGGAA[A/G]GGGGGAGGGAGAAAT | 8450 |
rs182970346 | snp | C/G | 0.0131573 | 0.0800346 | intron-variant | CUL4B | GRCh38.p7 | X:120566480 | TTGGCTCACCACAAC[C/G]TCCACCTCCCGGGTT | 8450 |
rs182976569 | snp | A/C/T | 0.00422943 | 0.0457911 | intron-variant | CUL4B | GRCh38.p7 | X:120548981 | TGACCTTCAGATTTC[A/C/T]GTAAGTTTCCTGTTA | 8450 |
rs182978680 | snp | C/T | 0.00475684 | 0.0485365 | intron-variant | CUL4B | GRCh38.p7 | X:120531639 | TGATTTTTGTATTTT[C/T]AGTAGAGACAGGGTA | 8450 |
rs183078048 | snp | C/T | 0.00844089 | 0.0644143 | intron-variant | CUL4B | GRCh38.p7 | X:120549359 | GAGTTCGAGACCACT[C/T]TGACCAACATAGTGA | 8450 |
rs183097025 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120551852 | TTCCATAACCCCAAG[G/T]TATCAGTCCAGTTTT | 8450 |
rs183099650 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120569251 | CCATCATGTTCTACT[A/C]CCTTAGTATACAAAG | 8450 |
rs183114462 | snp | A/C | 0.00197367 | 0.0313519 | intron-variant | CUL4B | GRCh38.p7 | X:120534601 | CCTGTTGAAGAAATA[A/C]AAGTGTTTAGTCATC | 8450 |
rs183407878 | snp | G/T | 0.00422943 | 0.0457911 | intron-variant | CUL4B | GRCh38.p7 | X:120552073 | TTACATATTATGCAT[G/T]GTTTTATTTAAATAT | 8450 |
rs183546136 | snp | A/C | 0.000529661 | 0.016265 | upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120577128 | ATATCTATAAATATA[A/C]TTTTTCCTCTTTTCT | 8450 |
rs183560146 | snp | A/T | 0.00188317 | 0.0306274 | intron-variant | CUL4B | GRCh38.p7 | X:120538238 | TTGTACATGTATAAT[A/T]TTTTAAAGTGGTAAA | 8450 |
rs183617052 | snp | C/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120570635 | AAGGATTTTCTATTC[C/T]TATTCTGCATGCAGA | 8450 |
rs183650902 | snp | A/G | 0.00422943 | 0.0457911 | intron-variant | CUL4B | GRCh38.p7 | X:120535097 | CACTTTAGGAAGCGG[A/G]GGCAGGGGGATAGCT | 8450 |
rs183652073 | snp | A/G | 0.000529661 | 0.016265 | upstream-variant-2KB, intron-variant | CUL4B | GRCh38.p7 | X:120563027 | ACTTTGTTTAAACAG[A/G]CCCACTTGTTTTTGT | 8450 |
rs183674741 | snp | C/T | 0.00475684 | 0.0485365 | intron-variant | CUL4B | GRCh38.p7 | X:120527082 | TTTTTTTTTTTGAGA[C/T]GGAGTCTCGCTCTGT | 8450 |
rs183730526 | snp | C/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120532735 | AACTTTTCTTTGTTC[C/T]AGCCAATGGCTTTTT | 8450 |
rs183735092 | snp | A/C | 0.00105904 | 0.0229869 | intron-variant | CUL4B | GRCh38.p7 | X:120549566 | AAGAAAAAAGAAGAG[A/C]AGAGCAGAGCAGAGC | 8450 |
rs183790829 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120555670 | GGATAGGCCAGGCGC[A/G]GTGGCTCACACCTGT | 8450 |
rs183811289 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | CUL4B | GRCh38.p7 | X:120541421 | GGAGAATCACTTGAA[C/T]CTGGGAGGCAGAGGT | 8450 |
rs183884823 | snp | A/G | 0.00422943 | 0.0457911 | intron-variant | CUL4B | GRCh38.p7 | X:120545754 | GCCCTCTGATTTACT[A/G]CTTGAGAAGTAACTG | 8450 |
rs184152911 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120557128 | GTTGGTCAGGCTGGT[C/T]TCGAACTCCTGACCT | 8450 |
rs184165694 | snp | C/T | 0.000529661 | 0.016265 | upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120576435 | TGATGGGATTCTATA[C/T]ATTTATTTTGCATCT | 8450 |
rs184244822 | snp | C/T | 6.47417e-05 | 0.00568917 | intron-variant, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120557917 | GGTTATGCATATTAA[C/T]ACATACCTGGTAGAG | 8450 |
rs184281977 | snp | A/G | 0.000529661 | 0.016265 | upstream-variant-2KB, intron-variant | CUL4B | GRCh38.p7 | X:120563480 | GGCCTCAAGTGATCC[A/G]CCTGCCTCAGCCTCC | 8450 |
rs184295959 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120527611 | GATACCATGGAGATG[C/G]GACCCAAGTCTAAAC | 8450 |
rs184297076 | snp | C/T | 0.0026455 | 0.0362733 | intron-variant | CUL4B | GRCh38.p7 | X:120546491 | CTGTATTTGAAGAAA[C/T]GTTTTTAACTATTAA | 8450 |
rs184395972 | snp | A/T | 0.00528398 | 0.051128 | intron-variant | CUL4B | GRCh38.p7 | X:120567443 | CAATTTAGATTTAAA[A/T]CCAGGGTTCCCAACT | 8450 |
rs184399717 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120542488 | TCTAAATTCACTTGG[A/G]ATTAGAAGTGCTTGG | 8450 |
rs184415297 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120546678 | ATGTGCCATGTGACA[C/G]AGAGCATATTAGTCT | 8450 |
rs184544059 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120563925 | AGTCCTGTTAATATT[C/T]AACTACATTCTAGTA | 8450 |
rs184566956 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120527958 | TGGTTAAATACAAAA[A/G]ACTACATTTATTGTA | 8450 |
rs184575385 | snp | A/G | | | intron-variant | CUL4B | GRCh38.p7 | X:120532080 | GTCATGAATTTAATT[A/G]CCCCAAAATGAACAG | 8450 |
rs184587238 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | CUL4B | GRCh38.p7 | X:120549877 | CTCAGCATTTCTTAT[C/T]GCTTTGCTTAGATTC | 8450 |
rs184589457 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120568107 | AGTCTTAGTTCCTAA[A/C]CCTTTAAGGTGAATG | 8450 |
rs184606036 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | CUL4B | GRCh38.p7 | X:120533458 | ACTCACTATTCTATG[C/T]TACAATTAAGCTCTT | 8450 |
rs184724672 | snp | C/T | 0.00896606 | 0.0663524 | intron-variant | CUL4B | GRCh38.p7 | X:120553492 | TAAAATTATTTTCAT[C/T]AGAATTGAAGTATGG | 8450 |
rs184725708 | snp | A/C | 0.00422943 | 0.0457911 | intron-variant | CUL4B | GRCh38.p7 | X:120528446 | TTAAAAGAATACTGG[A/C]CAGGTGCAGTGGCTC | 8450 |
rs184979699 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120569045 | TTGCATGCAGTTCAG[A/G]CCACCATCAAGCAGG | 8450 |
rs184987834 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | CUL4B | GRCh38.p7 | X:120550730 | CTGTTTTTCTAATTT[A/G]GCCTTGACTGCTTAA | 8450 |
rs185104475 | snp | C/G | 0.00475684 | 0.0485365 | intron-variant | CUL4B | GRCh38.p7 | X:120553619 | ATCTTAAACACTGTA[C/G]TAGGCCAGACATGGT | 8450 |
rs185105648 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120571358 | TATTGAAGGCAGACC[A/G]TGACAGTATGCAGAA | 8450 |
rs185114250 | snp | C/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120546946 | TTATTTACATGAATA[C/T]CACACGTAGTCCTGG | 8450 |
rs185121104 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120554710 | AGTAAGTGTTTACCT[C/T]AGAGAAAGAGGGTGG | 8450 |
rs185121325 | snp | G/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120572584 | AAACCAGCCCCCAAA[G/T]GTAACCTCAGTTAAG | 8450 |
rs185128848 | snp | A/G | 0.00422943 | 0.0457911 | intron-variant | CUL4B | GRCh38.p7 | X:120537772 | AAAGGCTTTTATACA[A/G]CTGCATTATCACTTC | 8450 |
rs185198412 | snp | A/G | 0.0317957 | 0.122012 | intron-variant | CUL4B | GRCh38.p7 | X:120571924 | ATTTTGGTATCTGCA[A/G]GGTTCCTGGAGCCAG | 8450 |
rs185227687 | snp | C/T | 0.00422943 | 0.0457911 | intron-variant | CUL4B | GRCh38.p7 | X:120537509 | AAGAGGGGAAAAGGG[C/T]AAAGCAGATAAGCCC | 8450 |
rs185240575 | snp | A/G | 0.00105904 | 0.0229869 | upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120576268 | TGGAATATAACAAAA[A/G]AATGTTAATTTTAAA | 8450 |
rs185248308 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120540890 | TAATCACAAAAATAG[C/T]AAGCAATGATCACTG | 8450 |
rs185368040 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120556857 | ACCAACATAATTTCT[C/T]ACAAGGTACTCATCA | 8450 |
rs185389157 | snp | C/T | 0.000205583 | 0.0101365 | synonymous-codon | CUL4B | GRCh38.p7 | X:120537011 | TAACTCAATATTTCC[C/T]GGAACATTCTGATTC | 8450 |
rs185733003 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120564476 | CTGGGCACGTTGGCA[A/G]GTGCCTGTAATCCCA | 8450 |
rs185848535 | snp | A/G | 0.000529661 | 0.016265 | intron-variant, utr-variant-5-prime | CUL4B | GRCh38.p7 | X:120559821 | TTGTCAGTGTTATAA[A/G]GAATAACAGATTAAA | 8450 |
rs185867059 | snp | C/T | 0.00211696 | 0.0324653 | utr-variant-3-prime | CUL4B | GRCh38.p7 | X:120526597 | TATTACTCTTTAAAA[C/T]GGGCATGTTAACCAC | 8450 |
rs185869258 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120544723 | ACTTCTTACCACATG[C/T]TCCCATGCTAATTAG | 8450 |
rs185880914 | snp | A/C | 0.0126344 | 0.0784702 | intron-variant | CUL4B | GRCh38.p7 | X:120551919 | ACTGTTTACTAAGTA[A/C]TCTTCATCCTATTAC | 8450 |
rs185887313 | snp | A/G/T | 0.00105904 | 0.0229869 | intron-variant | CUL4B | GRCh38.p7 | X:120569454 | CAAGCTCCGACTCCC[A/G/T]GGTTCACGCCATTCT | 8450 |
rs185983004 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | CUL4B | GRCh38.p7 | X:120548154 | TGGTGTGTACCTGTA[A/G]TTCCAGCTATTTAGG | 8450 |
rs186006625 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | CUL4B | GRCh38.p7 | X:120565021 | AAAGGAAGAAATACA[A/G]ACAAAGACAGGGAGC | 8450 |
rs186015001 | snp | C/T | 0.00422943 | 0.0457911 | intron-variant | CUL4B | GRCh38.p7 | X:120547772 | GGGAAGGCAGATCCA[C/T]CCTTAACCTGGTGGG | 8450 |
rs186017134 | snp | C/T | 0.0026455 | 0.0362733 | intron-variant | CUL4B | GRCh38.p7 | X:120529922 | CCCTTTTGTCACTGC[C/T]GCCCACATATGCCAA | 8450 |
rs186102606 | snp | C/T | 0.0105399 | 0.0718252 | intron-variant | CUL4B | GRCh38.p7 | X:120565813 | TCACTGCAAGCTCCG[C/T]CTCCCGGGTTCATGC | 8450 |
rs186122841 | snp | C/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120530870 | TCTTTAGTAATTAAA[C/T]CAAAAAAACAGTTTG | 8450 |
rs186145345 | snp | A/G | 0.000529661 | 0.016265 | utr-variant-3-prime | CUL4B | GRCh38.p7 | X:120525223 | GTCTTTGAGAACTCA[A/G]GCAAACAATCAACAG | 8450 |
rs186407582 | snp | A/G | 0.00370173 | 0.0428621 | intron-variant | CUL4B | GRCh38.p7 | X:120566127 | GAGATAGTAAAGATT[A/G]TATCATAATAAGGGC | 8450 |
rs186420543 | snp | C/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120572894 | ACAATTTCCTTTGTT[C/T]CTTTTTTCAACTATT | 8450 |
rs186515200 | snp | A/C | 0.00211696 | 0.0324653 | intron-variant | CUL4B | GRCh38.p7 | X:120568534 | TGTCCTTTATTCCCA[A/C]CAACAGCATTATTTC | 8450 |
rs186643274 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120555803 | AAAAACTAGCAGGGC[A/G]TGGTGGCAGGCGCCT | 8450 |
rs186653843 | snp | A/G | 0.00211696 | 0.0324653 | intron-variant | CUL4B | GRCh38.p7 | X:120553140 | AAGAGTAGAATTTTA[A/G]TTGTACATTTTAAAA | 8450 |
rs186659661 | snp | A/C | 0.00105904 | 0.0229869 | intron-variant | CUL4B | GRCh38.p7 | X:120571167 | GTTCTAGTTCTTACA[A/C]ACAGATGATAGATTC | 8450 |
rs186739824 | snp | A/G | 0.00317376 | 0.039709 | intron-variant | CUL4B | GRCh38.p7 | X:120550330 | CCAAGTGAATACATG[A/G]AGTATTCAAAAAAAA | 8450 |
rs186795599 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | CUL4B | GRCh38.p7 | X:120543354 | TTAGGAAGGTAAAGA[A/G]GTACTACATACAGAG | 8450 |
rs186799569 | snp | C/T | 0.00370173 | 0.0428621 | intron-variant | CUL4B | GRCh38.p7 | X:120556232 | ACTACAACTACTAGC[C/T]GACATTTGCATAGCA | 8450 |
rs186816190 | snp | C/G | 0.00105904 | 0.0229869 | intron-variant | CUL4B | GRCh38.p7 | X:120539796 | ATAAACCAGATACAT[C/G]GTAGAGTAGAAGGTA | 8450 |
rs186854136 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120573564 | GTGCCAACATATGAT[C/G]CCCACCTTCTGAATG | 8450 |
rs186860428 | snp | A/G | 0.00624608 | 0.055534 | intron-variant | CUL4B | GRCh38.p7 | X:120538246 | GTATAATATTTTAAA[A/G]TGGTAAAAACAAAAG | 8450 |
rs186992623 | snp | C/G | 0.0026455 | 0.0362733 | intron-variant | CUL4B | GRCh38.p7 | X:120535008 | CCACTCTATTCGTAG[C/G]TCCCAGCAACAAGAT | 8450 |
rs186998020 | snp | A/G | 0.000529661 | 0.016265 | intron-variant, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120559066 | TCTGCTTGAGACAAA[A/G]TAGAGCATACTCCTG | 8450 |
rs187136715 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120563595 | TGAACTTTCCTTTAT[C/T]GTGTCTCACAGTTCA | 8450 |
rs187143311 | snp | A/C/T | 0.00145554 | 0.0269379 | intron-variant | CUL4B | GRCh38.p7 | X:120546520 | AATACAATGTTTAGC[A/C/T]GAAATACAATACTTT | 8450 |
rs187144891 | snp | C/T | 0.0026455 | 0.0362733 | intron-variant | CUL4B | GRCh38.p7 | X:120527680 | CTGAAGATAATTTTA[C/T]ACCTTTTGTGCATGA | 8450 |
rs187248153 | snp | A/C | | | intron-variant | CUL4B | GRCh38.p7 | X:120540935 | TAACAGGGTATTATT[A/C]GAAGCCTCTGGGATC | 8450 |
rs187261886 | snp | C/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120549279 | GAAAGCTTGGCAGAG[C/T]GCGGTGGCTCACGCC | 8450 |
rs187263024 | snp | C/T | 0.00422943 | 0.0457911 | intron-variant | CUL4B | GRCh38.p7 | X:120566489 | CACAACGTCCACCTC[C/T]CGGGTTCAAGCGATT | 8450 |
rs187372732 | snp | A/T | 0.00422943 | 0.0457911 | intron-variant | CUL4B | GRCh38.p7 | X:120546030 | ACAGGATAATCATCA[A/T]GAGAGAAAAAAAAAT | 8450 |
rs187393119 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120527451 | GGGTCTTGCTATGTC[A/G]CCCAGGCTGACCTTA | 8450 |
rs187407491 | snp | G/T | 4.93815e-05 | 0.00496873 | intron-variant | CUL4B | GRCh38.p7 | X:120538234 | ATGTTTGTACATGTA[G/T]AATATTTTAAAGTGG | 8450 |
rs187503993 | snp | G/T | | | upstream-variant-2KB, intron-variant | CUL4B | GRCh38.p7 | X:120561587 | GAGGAGCGGGAAGGA[G/T]CCTCGGGGGAGGGAA | 8450 |
rs187647902 | snp | C/T | 0.00581083 | 0.0535878 | intron-variant | CUL4B | GRCh38.p7 | X:120555542 | ACAGGAGTAAAAGTG[C/T]AATGAACTAGAAATC | 8450 |
rs187753627 | snp | C/T | 0.000118154 | 0.00768526 | intron-variant | CUL4B | GRCh38.p7 | X:120545561 | AAGTTTTGTATGTTG[C/T]GAAGCTGAAATATTT | 8450 |
rs187869423 | snp | C/T | 0.0131573 | 0.0800346 | intron-variant | CUL4B | GRCh38.p7 | X:120532120 | AAACTATAAGAGCCA[C/T]GTAAAAATATTACAC | 8450 |
rs187915795 | snp | C/G | 0.0105399 | 0.0718252 | intron-variant | CUL4B | GRCh38.p7 | X:120548770 | ACCCAGGAGGTGGAG[C/G]GTGCAGTGAGCCGAG | 8450 |
rs187923296 | snp | C/T | 0.00422943 | 0.0457911 | intron-variant | CUL4B | GRCh38.p7 | X:120531236 | CTGAGGCAGGATAAT[C/T]GCTTGAACCTGGAAG | 8450 |
rs187969085 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | CUL4B | GRCh38.p7 | X:120549406 | AAAATACAAAAATTA[A/G]CCGGGTGTGGTGGTG | 8450 |
rs187969288 | snp | G/T | 0.00158814 | 0.0281345 | intron-variant | CUL4B | GRCh38.p7 | X:120554721 | ACCTCAGAGAAAGAG[G/T]GTGGGACAGGGGTTT | 8450 |
rs187971713 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | CUL4B | GRCh38.p7 | X:120572741 | ATCTTTCCTTGTCAC[C/T]ACACACAGATCTACC | 8450 |
rs187988102 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120537832 | TGCAAATTACCAAAC[G/T]ATAAGATGCTGAGGA | 8450 |
rs188105113 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120570638 | GATTTTCTATTCCTA[G/T]TCTGCATGCAGACTT | 8450 |
rs188134883 | snp | A/G | 0.00422943 | 0.0457911 | intron-variant | CUL4B | GRCh38.p7 | X:120535182 | CCTGGGTGACAGAGT[A/G]GGACCCTATCTCTAA | 8450 |
rs188216946 | snp | A/G | 0 | 0 | intron-variant | CUL4B | GRCh38.p7 | X:120556981 | CAATGGTGCAATCTC[A/G]GCTCACCGCAACCTC | 8450 |
rs188243380 | snp | G/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120567009 | GGCCTATTTTTAACA[G/T]TCTGTTTACTTTATC | 8450 |
rs188263653 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120531990 | AAAAATCTACTTCCA[C/T]AAATTTATCATATAT | 8450 |
rs188410911 | snp | A/G | | | intron-variant | CUL4B | GRCh38.p7 | X:120552438 | CAGGCGTCAGCCACC[A/G]CACCCAGCCTTACAA | 8450 |
rs188498305 | snp | A/G | 0.0152462 | 0.0859689 | upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120577080 | TTTTAATGTTTTTAA[A/G]TTACATTTCTTGGAT | 8450 |
rs188507391 | snp | A/G | 0.0126344 | 0.0784702 | upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120576400 | ATTTAATAATACTTT[A/G]AAAAGGAAAAAAATG | 8450 |
rs188512462 | snp | A/G | 0.00211696 | 0.0324653 | intron-variant | CUL4B | GRCh38.p7 | X:120557201 | CAGGTGTGAGCCACC[A/G]TGCCCGGCCTGAAGT | 8450 |
rs188531002 | snp | C/T | 2.27949e-05 | 0.00337593 | missense | CUL4B | GRCh38.p7 | X:120541654 | ACTCCACCTCGAACT[C/T]TACTGAAGAGCTGAT | 8450 |
rs188894175 | snp | A/T | 0.000529661 | 0.016265 | utr-variant-5-prime | CUL4B | GRCh38.p7 | X:120575753 | TTAAACAGATAAGCC[A/T]AGGTTGTTCTATACC | 8450 |
rs188907663 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120568178 | CTGGAGGTAAACAGA[A/T]CTAGAAGAAGCCACT | 8450 |
rs188921315 | snp | A/G | 0.000847358 | 0.020566 | intron-variant | CUL4B | GRCh38.p7 | X:120540359 | ACTGGAAAAAGGACT[A/G]GAAAACATACCTATA | 8450 |
rs189020846 | snp | A/G | 0.00528398 | 0.051128 | intron-variant | CUL4B | GRCh38.p7 | X:120564045 | TGGTGGCTCATGCCT[A/G]TAATCCCAGCACTTT | 8450 |
rs189025375 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | CUL4B | GRCh38.p7 | X:120528252 | TCTGTACTAAAAATA[C/T]AAGAATTAGCCAGGT | 8450 |
rs189047887 | snp | A/G | 0.000529661 | 0.016265 | upstream-variant-2KB, intron-variant | CUL4B | GRCh38.p7 | X:120563117 | TTGCTATTTGATGAC[A/G]GCCTGCTGAAAGCAA | 8450 |
rs189190850 | snp | C/T | 0.0168099 | 0.0901243 | intron-variant | CUL4B | GRCh38.p7 | X:120556734 | CCAAGATTATGAGGG[C/T]AACAGCAGTCAAAAC | 8450 |
rs189298127 | snp | G/T | 0.00105904 | 0.0229869 | intron-variant | CUL4B | GRCh38.p7 | X:120546708 | TTAAACATGAATACC[G/T]TGCACACTAAGTGAA | 8450 |
rs189417376 | snp | A/G | 0.0026455 | 0.0362733 | intron-variant | CUL4B | GRCh38.p7 | X:120564499 | TAATCCCAACTACTC[A/G]GGAGGATAAGGCAGA | 8450 |
rs189433189 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120571512 | TGGACTCTCTATGGT[C/T]CACAATATGGGGGCT | 8450 |
rs189448311 | snp | C/G | 0.0026455 | 0.0362733 | intron-variant | CUL4B | GRCh38.p7 | X:120528548 | CAATATGGTAAAACC[C/G]CGTCTCTACTAAAAA | 8450 |
rs189531374 | snp | A/G | 0.0100156 | 0.0700533 | intron-variant | CUL4B | GRCh38.p7 | X:120550387 | AAGGGCTTCTAGTAT[A/G]AGAAAAGTTGCCAGA | 8450 |
rs189572526 | snp | A/G | 0.00370173 | 0.0428621 | intron-variant | CUL4B | GRCh38.p7 | X:120567615 | CGGTGGCTCATGCCT[A/G]TGCCTGTAATCCCAG | 8450 |
rs189583376 | snp | A/G | | | intron-variant | CUL4B | GRCh38.p7 | X:120533029 | TTTACTATCAACTGT[A/G]GTTACGTCCAAAATT | 8450 |
rs189584637 | snp | A/C | 0.00158814 | 0.0281345 | intron-variant | CUL4B | GRCh38.p7 | X:120549571 | AAAAGAAGAGAAGAG[A/C]AGAGCAGAGCAGAGC | 8450 |
rs189679202 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120572549 | GGTGAAATCTCCACT[C/T]AGTCCCTGTTCCCCA | 8450 |
rs189694420 | snp | C/T | 0.00791544 | 0.0624105 | intron-variant | CUL4B | GRCh38.p7 | X:120537672 | AATTTGCCATCATTA[C/T]CACCTATGATCTTAA | 8450 |
rs189785474 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120568607 | AAATACTCTCAGCAA[C/T]GCATGGTGCTAGATG | 8450 |
rs189813581 | snp | C/T | 0.00475684 | 0.0485365 | intron-variant | CUL4B | GRCh38.p7 | X:120534236 | AAAATTAGCCAGGCA[C/T]GGTGGCATGCACTTG | 8450 |
rs189829130 | snp | A/C | 0.00422943 | 0.0457911 | intron-variant | CUL4B | GRCh38.p7 | X:120533544 | CCCATTCCTACCTCC[A/C]AACCTCATCTCAAAA | 8450 |
rs189953716 | snp | C/T | 0.00528398 | 0.051128 | intron-variant | CUL4B | GRCh38.p7 | X:120554074 | TAGAATTTAAAATCG[C/T]GTGGCTTCAGAGCTC | 8450 |
rs190012893 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120574764 | AAGGAAATTATCAAA[A/G]TTTTGGTCTGCTAAT | 8450 |
rs190021180 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | CUL4B | GRCh38.p7 | X:120556558 | TAAATTGAGAGTGAC[A/G]GCTGGGTTTGGTAGC | 8450 |
rs190071845 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | CUL4B | GRCh38.p7 | X:120549879 | CAGCATTTCTTATCG[C/T]TTTGCTTAGATTCTG | 8450 |
rs190182456 | snp | A/C | 0.000113947 | 0.00754722 | synonymous-codon, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120560120 | CTTCTTAGCAGAGCC[A/C]GGTTTGCTGTTAGCA | 8450 |
rs190193203 | snp | C/T | 0.00370173 | 0.0428621 | intron-variant | CUL4B | GRCh38.p7 | X:120544868 | GAAGCTAAATTCCTA[C/T]TTTCCTCCATAACTA | 8450 |
rs190309436 | snp | A/G | 0.00738971 | 0.0603345 | intron-variant | CUL4B | GRCh38.p7 | X:120538591 | AAGAGGAAATCGATT[A/G]AAAGGGTAAAAAGCT | 8450 |
rs190324236 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120547851 | AAAAGGAGAGAAGGG[C/T]CTAGCCTCCCAGCCT | 8450 |
rs190330514 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120565054 | GCTTTTACAATGTCA[A/G]TTCCTTTATTTCTGT | 8450 |
rs190361436 | snp | G/T | 0.00738971 | 0.0603345 | intron-variant | CUL4B | GRCh38.p7 | X:120553506 | TCAGAATTGAAGTAT[G/T]GCCTAGGCTTGACTT | 8450 |
rs190448731 | snp | A/G | 0.000529661 | 0.016265 | intron-variant, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120559297 | ATAAAAATTAATTCA[A/G]CTCAAATACATTTTT | 8450 |
rs190456792 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120543408 | ACTTAGGAAAGCACA[A/G]AAATAGGGGAATCCA | 8450 |
rs190469409 | snp | A/G | 0.000529661 | 0.016265 | utr-variant-3-prime | CUL4B | GRCh38.p7 | X:120525381 | TAAACAAAATTTTCT[A/G]CTTCTCCTCCCTTCA | 8450 |
rs190477542 | snp | G/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120542538 | CAAAAAACCCTCACC[G/T]CTTTAGTGTAAAAAG | 8450 |
rs190599298 | snp | C/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120530914 | AGTTTCTTCCTGGTA[C/T]AGCATAAATGTTTTA | 8450 |
rs190634692 | snp | A/C | 0.00370173 | 0.0428621 | intron-variant | CUL4B | GRCh38.p7 | X:120537436 | CCAGCCCAAGTCTCC[A/C]GTTTTTCACTTGCTC | 8450 |
rs190730293 | snp | C/T | | | intron-variant, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120558444 | AGCCTCTTAATCTTC[C/T]CAACAATACCCTGAG | 8450 |
rs190747316 | snp | A/T | 0.000529661 | 0.016265 | downstream-variant-500B | CUL4B | GRCh38.p7 | X:120524204 | TCTTACTCTGAGAGT[A/T]TCTGGCCCAGAACTC | 8450 |
rs190825497 | snp | A/G | 0.0173306 | 0.0914601 | intron-variant | CUL4B | GRCh38.p7 | X:120531521 | CTGCAGTGCAGTGGC[A/G]CGATCTCAGCTCACT | 8450 |
rs190827523 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | CUL4B | GRCh38.p7 | X:120548812 | GCACTCCAGCCTGGG[C/T]AACAGAGAGAGACTC | 8450 |
rs190836538 | snp | C/G | | | intron-variant | CUL4B | GRCh38.p7 | X:120548201 | ATCACTTGAGCCCAA[C/G]AGTTCAAGGTTGAAG | 8450 |
rs190960382 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120550944 | ATATAAAACATCTCT[A/G]GAAAGATACCCAAAA | 8450 |
rs190965812 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120569223 | AAACAGTGAAGGAAC[C/T]CTGCCGGCAGACCCA | 8450 |
rs190973509 | snp | C/T | 0.00528398 | 0.051128 | intron-variant | CUL4B | GRCh38.p7 | X:120565835 | GGTTCATGCCATTCT[C/T]CTGCCTCAGCCTCCC | 8450 |
rs190974499 | snp | C/G | 0.00295878 | 0.0383488 | intron-variant | CUL4B | GRCh38.p7 | X:120534448 | TTAACATAGTGGTGT[C/G]CACATAGTGAACAAT | 8450 |
rs191126833 | snp | C/T | 0.000529661 | 0.016265 | utr-variant-3-prime | CUL4B | GRCh38.p7 | X:120526666 | TGCTTCATTTGGTCA[C/T]CGGTAGTAAAAAAGG | 8450 |
rs191245076 | snp | A/G | 0.00370173 | 0.0428621 | intron-variant | CUL4B | GRCh38.p7 | X:120574027 | AGACGGGGTTTCACA[A/G]TGTTGGCCAGGCTGC | 8450 |
rs191383673 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120535025 | CCCAGCAACAAGATT[A/T]CTGTCAAGAAGTGGC | 8450 |
rs191490370 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120556156 | TACATTTTAAGAGAC[A/G]CATATATAATACGCC | 8450 |
rs191519056 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | CUL4B | GRCh38.p7 | X:120530003 | TTTTCTCTCTCTAAA[C/T]GGTCATGACGCTTTA | 8450 |
rs191576561 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120563639 | CACTGTAAATGCAGG[A/G]TAAATGCTTATTGAA | 8450 |
rs191612966 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120540258 | ATACCAGCTAAGCAA[A/C]CTCAAACAAATCAGG | 8450 |
rs191699628 | snp | C/T | 0.0142023 | 0.083063 | intron-variant | CUL4B | GRCh38.p7 | X:120556988 | GCAATCTCGGCTCAC[C/T]GCAACCTCTACCTCC | 8450 |
rs191704047 | snp | A/G | 0.000529661 | 0.016265 | upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120576402 | TTAATAATACTTTGA[A/G]AAGGAAAAAAATGGA | 8450 |
rs191705957 | snp | A/C | 0.00158814 | 0.0281345 | intron-variant | CUL4B | GRCh38.p7 | X:120541082 | TGCTTTAAGTGGTAG[A/C]GACAGAAATTATGTC | 8450 |
rs191729349 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | CUL4B | GRCh38.p7 | X:120566642 | CCTCAGGTGATCTGC[C/T]TGCCTCAGCTTCCCA | 8450 |
rs191765651 | snp | C/T | 0.0026455 | 0.0362733 | intron-variant | CUL4B | GRCh38.p7 | X:120570036 | AGCTAATGAAGGAAA[C/T]GAAGGCAGCATCCCA | 8450 |
rs191921254 | snp | G/T | 0.00211696 | 0.0324653 | intron-variant | CUL4B | GRCh38.p7 | X:120555652 | TCCTCATCAATAAAG[G/T]GGGGATAGGCCAGGC | 8450 |
rs192007257 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120545640 | TTACTAAGATCAAAC[A/T]TGCAGATAAACACAT | 8450 |
rs192075390 | snp | G/T | 0.0168099 | 0.0901243 | intron-variant | CUL4B | GRCh38.p7 | X:120552059 | TTATTTATGTATTTT[G/T]ACATATTATGCATTG | 8450 |
rs192211056 | snp | A/T | 0.00105904 | 0.0229869 | intron-variant | CUL4B | GRCh38.p7 | X:120572929 | TTTTGGAAGTTCTAC[A/T]TACTATTTACATTCT | 8450 |
rs192247022 | snp | A/G | 7.41409e-05 | 0.0060881 | intron-variant | CUL4B | GRCh38.p7 | X:120538235 | TGTTTGTACATGTAT[A/G]ATATTTTAAAGTGGT | 8450 |
rs192261231 | snp | A/C | 0.00105904 | 0.0229869 | upstream-variant-2KB, intron-variant | CUL4B | GRCh38.p7 | X:120563426 | ATTTTTAGTAGAGTC[A/C]GGGTTTTGCTATGTT | 8450 |
rs192284668 | snp | A/G | 0.00422943 | 0.0457911 | intron-variant | CUL4B | GRCh38.p7 | X:120546219 | TTCCAATTCAGAAAA[A/G]GAACTTGGGAGGAAG | 8450 |
rs192290446 | snp | A/G | 0.00422943 | 0.0457911 | intron-variant | CUL4B | GRCh38.p7 | X:120527484 | CTCTTGTTCTGGAGT[A/G]ATCCCCCCAGCCTCA | 8450 |
rs192355705 | snp | C/G | 0.000529661 | 0.016265 | upstream-variant-2KB, intron-variant | CUL4B | GRCh38.p7 | X:120561929 | CAAGGCACCACAGAC[C/G]CAAGGCTGAATAAGG | 8450 |
rs192359681 | snp | A/G | | | intron-variant | CUL4B | GRCh38.p7 | X:120527041 | ACCAGGTTAAAAAAT[A/G]TTTTATACACGTTGA | 8450 |
rs192428804 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120567796 | GGGAGGATTGCTTGA[A/G]CCCAGGAGTTCCAGC | 8450 |
rs192472163 | snp | A/C | 0.0068637 | 0.0581785 | intron-variant | CUL4B | GRCh38.p7 | X:120567398 | TCCCAAAGTGGTAGG[A/C]TTACAGGCATGAGCC | 8450 |
rs192503933 | snp | A/T | 0.00422943 | 0.0457911 | intron-variant | CUL4B | GRCh38.p7 | X:120532322 | CACAAAAAATATTAA[A/T]GGTATTGGCAGTATT | 8450 |
rs192542859 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120553344 | AACCAGATTTTACAA[C/T]TGATAATAACCTATA | 8450 |
rs192544694 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | CUL4B | GRCh38.p7 | X:120571297 | TTAAAATTAAAAAAA[C/T]TAAAAGGTTTTTTTA | 8450 |
rs192558088 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | CUL4B | GRCh38.p7 | X:120536766 | TTCGGAAGGCTGAGG[C/T]GGGGGGGATCACTTG | 8450 |
rs192636960 | snp | C/G | 0.00422943 | 0.0457911 | intron-variant | CUL4B | GRCh38.p7 | X:120527715 | AAGTTTTGACTGCAA[C/G]CTGTCAAATGAGGTA | 8450 |
rs192643572 | snp | A/T | 0.0276852 | 0.114351 | intron-variant | CUL4B | GRCh38.p7 | X:120552693 | AACACAGTCAAAAAA[A/T]ATATATAAACGTGTA | 8450 |
rs192730180 | snp | C/G | 0.00422943 | 0.0457911 | intron-variant | CUL4B | GRCh38.p7 | X:120549357 | TGGAGTTCGAGACCA[C/G]TCTGACCAACATAGT | 8450 |
rs192802101 | snp | A/G | 0.0126344 | 0.0784702 | intron-variant | CUL4B | GRCh38.p7 | X:120549418 | TTAGCCGGGTGTGGT[A/G]GTGTGCACCAGCTAC | 8450 |
rs192860595 | snp | A/G | 0.00291242 | 0.038049 | intron-variant | CUL4B | GRCh38.p7 | X:120546628 | ATCCCTGAAACATAT[A/G]TTAAGGATATTTTAA | 8450 |
rs192864986 | snp | A/G | 0.0115877 | 0.0752302 | intron-variant | CUL4B | GRCh38.p7 | X:120570644 | CTATTCCTATTCTGC[A/G]TGCAGACTTCAAAGG | 8450 |
rs192937702 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120532032 | ATTTAGTTTCAAAGA[A/G]GTTTCTTGCAATCTT | 8450 |
rs192971560 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | CUL4B | GRCh38.p7 | X:120571662 | AGGCATGAGAAAGAT[C/T]ATGGCCCATTTAGGC | 8450 |
rs192987297 | snp | A/G | 0.00370173 | 0.0428621 | intron-variant | CUL4B | GRCh38.p7 | X:120537473 | CTGTCTGCAGGGAGT[A/G]ACCTGGAGTAGGGAA | 8450 |
rs193056401 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | CUL4B | GRCh38.p7 | X:120556824 | TGCAACTAAAATATA[C/T]AAATACTGATAAATA | 8450 |
rs193194790 | snp | A/G | | | intron-variant | CUL4B | GRCh38.p7 | X:120553563 | AGATAAATGTTACAC[A/G]CTCCTGTACAAACTT | 8450 |
rs193226676 | snp | A/G | 0.00105904 | 0.0229869 | upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120576145 | TGAGAGACAAGTTTT[A/G]TTAAGGCTTTAGTCT | 8450 |
rs193230251 | snp | A/G | 0.00322169 | 0.0400058 | intron-variant | CUL4B | GRCh38.p7 | X:120540597 | CTTTTTACTGTAATC[A/G]AATTGTCTACAATGA | 8450 |
rs199575215 | snp | A/C | 9.51e-05 | 0.00689499 | synonymous-codon | CUL4B | GRCh38.p7 | X:120544144 | TAATTTTTGGCCTTC[A/C]GCTGCATAGAGCCGG | 8450 |
rs199626491 | snp | C/G | | | intron-variant, utr-variant-5-prime | CUL4B | GRCh38.p7 | X:120559844 | AGATTAAATACAATA[C/G]GTTGAAAAAGACCTC | 8450 |
rs199796372 | snp | A/G | 4.10593e-05 | 0.00453078 | intron-variant | CUL4B | GRCh38.p7 | X:120539384 | TTAGCTAAAATGGGG[A/G]AAAAGTTTGTTGTTT | 8450 |
rs199865454 | in-del | -/GTGT | 0.0199298 | 0.0978146 | utr-variant-3-prime | CUL4B | GRCh38.p7 | X:120526426 | GCTTCATAATTAATG[-/GTGT]GTAAGAACCCTCCCC | 8450 |
rs199927369 | snp | C/T | 0.000529661 | 0.016265 | synonymous-codon | CUL4B | GRCh38.p7 | X:120545461 | AATGGAGGGTAGCAT[C/T]GAATTCTGAAGAACG | 8450 |
rs200034623 | snp | C/T | 2.27912e-05 | 0.00337566 | missense | CUL4B | GRCh38.p7 | X:120574566 | CACCGTCTTTAGAGG[C/T]AGTAGCCTCATCATC | 8450 |
rs200063914 | snp | A/G | 0.00528398 | 0.051128 | intron-variant | CUL4B | GRCh38.p7 | X:120570964 | TGGGAGGCTGAGGCA[A/G]GAGGATCGCTTGAGC | 8450 |
rs200250781 | snp | A/C | | | upstream-variant-2KB, intron-variant | CUL4B | GRCh38.p7 | X:120563085 | AAATCAACCTTTGGC[A/C]TTATTAGACAATATC | 8450 |
rs200296520 | snp | A/C | 3.61454e-05 | 0.00425105 | synonymous-codon | CUL4B | GRCh38.p7 | X:120539314 | ATCCAACATTTTCTC[A/C]AGTTCTTCATCTGTA | 8450 |
rs200413217 | snp | A/G | 6.99056e-05 | 0.00591168 | synonymous-codon | CUL4B | GRCh38.p7 | X:120547168 | CTGTGCTTTGATGTG[A/G]TCTTCGCAGATCTGT | 8450 |
rs200449582 | snp | A/T | | | intron-variant, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120557873 | CAAAATCCATATACA[A/T]CCCACCTCAATTTAT | 8450 |
rs200461872 | in-del | -/A | 0.0421602 | 0.138934 | intron-variant | CUL4B | GRCh38.p7 | X:120547124 | ACGATTTTTTGTTTT[-/A]AAAAAGGATATTCTC | 8450 |
rs200768115 | snp | C/T | 4.59195e-05 | 0.00479141 | intron-variant | CUL4B | GRCh38.p7 | X:120544455 | TAGCAATCAGCTCTG[C/T]ATAGTAGGTGTAGTA | 8450 |
rs200786671 | in-del | -/C | 0.0068637 | 0.0581785 | intron-variant | CUL4B | GRCh38.p7 | X:120537388 | TATGTGGCTTAAACA[-/C]CCTTGCAGCAACCCC | 8450 |
rs200896776 | in-del | -/TTCAACCGATT | 0.32505 | 0.238469 | intron-variant | CUL4B | GRCh38.p7 | X:120552244 | CCTCTGCCTCCTGGG[-/TTCAACCGATT]CTCATGCCTTAGCCT | 8450 |
rs201325911 | snp | A/G | 0.000235448 | 0.0108475 | intron-variant | CUL4B | GRCh38.p7 | X:120547112 | GACAAAACTATTCAC[A/G]ATTTTTTGTTTTAAA | 8450 |
rs201491482 | in-del | -/TTAG | 0.0816601 | 0.184829 | intron-variant | CUL4B | GRCh38.p7 | X:120572970 | ACGTTTCAGTTCTGT[-/TTAG]TTATGCAAATGATAT | 8450 |
rs201566181 | snp | A/G | 0.000313014 | 0.0125063 | synonymous-codon | CUL4B | GRCh38.p7 | X:120546601 | CTTTAAAAAAAGAAC[A/G]CTATCCAATGAATCC | 8450 |
rs201582033 | snp | A/G | | | intron-variant | CUL4B | GRCh38.p7 | X:120573888 | GAGTGCAATGGCACA[A/G]TCTCTGCTCACTGCA | 8450 |
rs201629851 | snp | A/G | 0.00160454 | 0.0282789 | intron-variant | CUL4B | GRCh38.p7 | X:120543052 | CAAGGAAAAAAAAAA[A/G]GGTTAGTATTATTGA | 8450 |
rs202209674 | snp | A/G | | | synonymous-codon | CUL4B | GRCh38.p7 | X:120534550 | ACATTAGCAGCACCA[A/G]TGTTTGAAAAAGAGA | 8450 |
rs202223692 | in-del | -/ACACACAC | | | intron-variant | CUL4B | GRCh38.p7 | X:120543496 | TAAATTACCTTCTAA[-/ACACACAC]ACACACACACACACA | 8450 |
rs267606335 | snp | A/G | | | missense | CUL4B | GRCh38.p7 | X:120541631 | TCCACTGCTGCAAAA[A/G]AACCTGAACTCCACC | 8450 |
rs367642288 | snp | A/T | 0.00211696 | 0.0324653 | intron-variant | CUL4B | GRCh38.p7 | X:120534252 | GGTGGCATGCACTTG[A/T]AGTCCCATCTGCTTG | 8450 |
rs367660624 | snp | C/T | 7.72171e-05 | 0.0062131 | missense | CUL4B | GRCh38.p7 | X:120545475 | TTGAATTCTGAAGAA[C/T]GTAAGTTCTATCCAG | 8450 |
rs367675981 | snp | C/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120553188 | TGATTAACGATTCAG[C/T]AAAAAGAGAAATACA | 8450 |
rs367762561 | snp | A/C/G/T | 0.00183508 | 0.0302474 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | CUL4B | GRCh38.p7 | X:120561442 | CCGCAGGACTTGAGT[A/C/G/T]GGGGGGGGAAGGGGG | 8450 |
rs367802852 | snp | C/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120541542 | AAATGCTTGCCAATA[C/T]GCACTCTTGATGTGT | 8450 |
rs367822733 | snp | A/G | 0.000529661 | 0.016265 | upstream-variant-2KB, intron-variant | CUL4B | GRCh38.p7 | X:120562799 | GTAGGATGTCTGGCT[A/G]GGAGTAAGGAAGATG | 8450 |
rs367874506 | snp | C/T | 2.55392e-05 | 0.00357337 | synonymous-codon | CUL4B | GRCh38.p7 | X:120546589 | TCTATCAATCTTCTT[C/T]AAAAAAAGAACGCTA | 8450 |
rs368184327 | snp | C/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120570979 | GGAGGATCGCTTGAG[C/T]CCAGGAGTTCGAGAC | 8450 |
rs368304478 | snp | A/G | 0.000189982 | 0.00974448 | synonymous-codon | CUL4B | GRCh38.p7 | X:120538145 | GAACTGAATCATGAT[A/G]TCTTTAGAAAGTTCC | 8450 |
rs368424714 | snp | A/G | 0.00633741 | 0.0559334 | intron-variant | CUL4B | GRCh38.p7 | X:120569522 | CCCGCCACCACGCCC[A/G]GCTAACTTTTTATAT | 8450 |
rs368451213 | snp | C/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120565178 | AGGACGCCATACAGT[C/T]ATAGCCATCTGGGGT | 8450 |
rs368517538 | snp | A/G | 0.000189982 | 0.00974449 | intron-variant | CUL4B | GRCh38.p7 | X:120544471 | ATAGTAGGTGTAGTA[A/G]TTAACTTACTTGCAA | 8450 |
rs368566396 | snp | C/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120536753 | GTAATCCCAGCACTT[C/T]GGAAGGCTGAGGCGG | 8450 |
rs368585828 | in-del | -/CT | 0.00422943 | 0.0457911 | intron-variant | CUL4B | GRCh38.p7 | X:120574705 | ATGAATTCATTGACT[-/CT]GGTTTCCCAGCCAAT | 8450 |
rs368671351 | snp | A/G | | | intron-variant | CUL4B | GRCh38.p7 | X:120527625 | GGGACCCAAGTCTAA[A/G]CACAAAATTCATCTA | 8450 |
rs368698473 | snp | C/G | | | intron-variant | CUL4B | GRCh38.p7 | X:120552250 | CCTCCTGGGTTCAAC[C/G]GATTCTCATGCCTTA | 8450 |
rs368789502 | snp | A/G | | | intron-variant | CUL4B | GRCh38.p7 | X:120531179 | ATACAAAAATTAGCC[A/G]GGCATGGTCGCTCAC | 8450 |
rs368919276 | snp | A/G | 0.00011396 | 0.00754765 | intron-variant | CUL4B | GRCh38.p7 | X:120534446 | TCTTAACATAGTGGT[A/G]TGCACATAGTGAACA | 8450 |
rs368960674 | snp | C/G | 2.392e-05 | 0.00345824 | missense, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120560480 | AAAGTCTTCTCTCTC[C/G]TTACTACTGTTACTG | 8450 |
rs368996955 | snp | C/T | 3.78158e-05 | 0.00434815 | intron-variant, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120557878 | TCCATATACATCCCA[C/T]CTCAATTTATGTTAA | 8450 |
rs369001194 | snp | A/G | | | intron-variant | CUL4B | GRCh38.p7 | X:120545213 | AACTTTAGTCCCCTC[A/G]GCTAACAAAAAACTT | 8450 |
rs369022718 | snp | A/G | | | intron-variant | CUL4B | GRCh38.p7 | X:120566246 | TCCCATCCTGAGATT[A/G]CTATATAAAAGCAAG | 8450 |
rs369046958 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | CUL4B | GRCh38.p7 | X:120539514 | TAAAAGTCTCCAAAG[C/T]CAGGAAGATCAACTG | 8450 |
rs369062636 | in-del | -/G | | | intron-variant | CUL4B | GRCh38.p7 | X:120541273 | GGAGGCCAAGGCGGG[-/G]TGGATCATTTGAGTT | 8450 |
rs369071353 | snp | C/T | | | intron-variant, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120558389 | ACATGAATTTTTAAC[C/T]TGAGATTTAAAGTAC | 8450 |
rs369160780 | snp | A/G | | | intron-variant | CUL4B | GRCh38.p7 | X:120557042 | TCAGCCTCCTGAGTA[A/G]CTGGGATTACAGGCA | 8450 |
rs369196487 | snp | A/C | | | intron-variant | CUL4B | GRCh38.p7 | X:120543617 | TGAAAACAACTGTTA[A/C]CACTTCAAATCACAC | 8450 |
rs369210448 | snp | A/G | 6.92241e-05 | 0.00588279 | synonymous-codon | CUL4B | GRCh38.p7 | X:120540461 | CTCATTCTTCAGAAA[A/G]CAGATATCAATTATA | 8450 |
rs369224624 | in-del | -/C | | | intron-variant | CUL4B | GRCh38.p7 | X:120535737 | AAAAAAAGAAGAAAA[-/C]AAAAAACAATAGCCT | 8450 |
rs369315556 | snp | C/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120565245 | TTGCCACTAGACAGA[C/T]ACTCCTGGAAGCCTT | 8450 |
rs369335804 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120552931 | TAAATATGGCTAAGA[C/T]ACTCTAAGTATTCAA | 8450 |
rs369379005 | snp | C/G | | | intron-variant | CUL4B | GRCh38.p7 | X:120572038 | GAAGACAGAGAGGTG[C/G]GGTGGGTTCAGATCA | 8450 |
rs369544628 | snp | A/T | 4.56142e-05 | 0.00477546 | intron-variant | CUL4B | GRCh38.p7 | X:120541563 | CTTGATGTGTAGATA[A/T]GCCATAAGAGAGAAA | 8450 |
rs369616947 | snp | C/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120574425 | CCGTGGTCTCGATCT[C/T]CTGACCTCGTGATCT | 8450 |
rs369619657 | in-del | -/A | | | intron-variant | CUL4B | GRCh38.p7 | X:120552679 | TGTCTGAAAAAAAAA[-/A]CACAGTCAAAAAATA | 8450 |
rs369641249 | snp | C/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120555017 | AAAAGAGCTAAAAAC[C/T]AATGCTTTTGAATTC | 8450 |
rs369645869 | snp | C/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120555889 | GGAGGTTGCAGTGAG[C/T]CGAGATCACGCCACT | 8450 |
rs369673689 | snp | A/G | 9.31966e-05 | 0.00682566 | intron-variant | CUL4B | GRCh38.p7 | X:120536892 | AATGCTATGATTTCT[A/G]TGCCTATAACTCAGT | 8450 |
rs369832790 | snp | A/C | | | intron-variant | CUL4B | GRCh38.p7 | X:120532679 | GCTTCCACTCCATCC[A/C]CCTATTAAAACTATT | 8450 |
rs369845412 | snp | A/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120573115 | AGTGTCTTTTACCTG[A/T]TAAATTTGGTGCATC | 8450 |
rs369861461 | in-del | -/AAG | | | intron-variant | CUL4B | GRCh38.p7 | X:120552799 | TCTGGTCACTGGTCT[-/AAG]GAGTGGAGTCTTAGT | 8450 |
rs370087735 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120536124 | AAATGGGATTTATTA[A/G]GATTTATACCTTTTG | 8450 |
rs370123375 | snp | A/C | 0.0110639 | 0.0735497 | upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120576824 | TACCACTTGGAGCTA[A/C]CACTGAGTCCAATGG | 8450 |
rs370280597 | snp | A/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120570487 | TTTGACAGAGACCGT[A/T]TGGCCCACAGAGTCT | 8450 |
rs370341614 | snp | A/G | 0.000189982 | 0.00974449 | intron-variant, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120560038 | CACGTGACCCCTCGA[A/G]TGTCAAATCCTTATT | 8450 |
rs370414632 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120548982 | GACCTTCAGATTTCC[C/G]TAAGTTTCCTGTTAT | 8450 |
rs370421802 | snp | C/G | 0.000139273 | 0.00834367 | intron-variant | CUL4B | GRCh38.p7 | X:120538072 | AAATCATAGCAAGCA[C/G]ATAACTAAATACAAC | 8450 |
rs370454387 | snp | C/T | 5.51739e-05 | 0.00525204 | intron-variant | CUL4B | GRCh38.p7 | X:120544089 | GAGAGACAGTGAGAA[C/T]TTATTAGTCATGATT | 8450 |
rs370557463 | snp | C/T | 0.00105904 | 0.0229869 | upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120576003 | TCTAGGCTCCTGTTC[C/T]GCCATTGCTGGCTTG | 8450 |
rs370664225 | in-del | -/A | 0.441884 | 0.160251 | upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120577598 | AGCGAGACCATGGCC[-/A]AAAAAAAAAAAAAAA | 8450 |
rs371003649 | snp | C/G | 9.74279e-05 | 0.00697886 | intron-variant | CUL4B | GRCh38.p7 | X:120545393 | CATTAGTGTAATTAA[C/G]ATTTGAGTATGATTT | 8450 |
rs371108039 | snp | C/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120571773 | AGTCGGCCCTCTGCA[C/T]GGGCGGGTTCCACAT | 8450 |
rs371143168 | snp | C/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120527939 | GAAGCAGCTACCCTT[C/T]GCGTGGTTAAATACA | 8450 |
rs371199111 | snp | C/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120537400 | AACACCTTGCAGCAA[C/T]CCCCATTCCTCACCC | 8450 |
rs371291880 | snp | A/T | 2.75843e-05 | 0.00371368 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120560670 | ACAGGCAGAGGAGCA[A/T]CAAAAACCTACGTTT | 8450 |
rs371296547 | snp | A/G | | | intron-variant | CUL4B | GRCh38.p7 | X:120542158 | TAGCATGATAGATTA[A/G]AGGCAAAAACAAACT | 8450 |
rs371312556 | snp | A/G | 0.000189982 | 0.00974449 | synonymous-codon, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120560369 | TACGTGGCTGGAAGC[A/G]GCCACTGAAACCCCC | 8450 |
rs371516079 | snp | C/T | 2.32132e-05 | 0.00340676 | intron-variant | CUL4B | GRCh38.p7 | X:120537059 | GATCAAAACACACAC[C/T]GAGATCTTAAAACTG | 8450 |
rs371556949 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | CUL4B | GRCh38.p7 | X:120552375 | CTGGTCTTGAATGCC[C/T]GACCTCAGGTGATCC | 8450 |
rs371637573 | snp | A/C | 2.82155e-05 | 0.00375592 | intron-variant | CUL4B | GRCh38.p7 | X:120540589 | AATTACCACTTTTTA[A/C]TGTAATCGAATTGTC | 8450 |
rs371699560 | snp | G/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120574075 | CAGGTGATCCTCCCC[G/T]CCAACCCCTCCTCCC | 8450 |
rs371753721 | in-del | -/G | | | intron-variant | CUL4B | GRCh38.p7 | X:120535729 | AAAAAAAAAAAAAAA[-/G]AAGAAAACAAAAAAC | 8450 |
rs371783408 | snp | A/G | 0.00211696 | 0.0324653 | intron-variant | CUL4B | GRCh38.p7 | X:120565616 | GAACCCGGGAGGCAG[A/G]GGTTGCAGTGAGCCG | 8450 |
rs371834066 | snp | A/G | | | intron-variant | CUL4B | GRCh38.p7 | X:120556028 | CTTATATGAGATAAT[A/G]CGAGATGAATCCCCT | 8450 |
rs371888106 | snp | C/G | | | intron-variant | CUL4B | GRCh38.p7 | X:120529507 | CAAGGGTTTGGCTAT[C/G]TACCTCCTAAAACTT | 8450 |
rs371931315 | snp | C/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120535162 | ATTGTGCCACTGTAC[C/T]CCTGCCTGGGTGACA | 8450 |
rs371942980 | snp | A/G | | | intron-variant | CUL4B | GRCh38.p7 | X:120564348 | AGGTGGCTCAGGCTT[A/G]TAATCCCAAAACTTT | 8450 |
rs371983788 | snp | G/T | 6.84221e-05 | 0.00584862 | intron-variant | CUL4B | GRCh38.p7 | X:120574501 | CCGCGCCCGGCCTGT[G/T]AACAATTATTTAGAC | 8450 |
rs372030366 | snp | A/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120574422 | TCACCGTGGTCTCGA[A/T]CTCCTGACCTCGTGA | 8450 |
rs372169750 | snp | A/G | 2.28475e-05 | 0.00337983 | utr-variant-3-prime | CUL4B | GRCh38.p7 | X:120526732 | CACTGGCTACTGCAT[A/G]TGACACCAAATGCTG | 8450 |
rs372205600 | snp | C/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120538965 | CTTTATTGTAAAACT[C/T]TTTTGCATGTAACTG | 8450 |
rs372394678 | snp | C/T | 6.73786e-05 | 0.00580386 | intron-variant, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120557911 | AAATCTGGTTATGCA[C/T]ATTAATACATACCTG | 8450 |
rs372453386 | snp | C/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120545956 | AATGGAAAAGGTTGT[C/T]ATCTGAATAAACTAA | 8450 |
rs372609218 | snp | A/T | 0.000273707 | 0.0116952 | intron-variant | CUL4B | GRCh38.p7 | X:120574645 | TCTACGATAGAAAAC[A/T]GAGAATTCACTTTTC | 8450 |
rs372653264 | snp | A/G | | | intron-variant | CUL4B | GRCh38.p7 | X:120575174 | CGAGCTTTTCCCTAA[A/G]TTATCCGCATCACAG | 8450 |
rs372778240 | snp | A/T | | | upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120576071 | GCATTTGGCTTGACT[A/T]GATTAGCTATCTAAA | 8450 |
rs372816351 | snp | A/T | 2.29331e-05 | 0.00338616 | missense | CUL4B | GRCh38.p7 | X:120538746 | GCTAAATCTTTCTTA[A/T]AGAAGGCCTCAAAAA | 8450 |
rs372899130 | snp | C/T | 2.2791e-05 | 0.00337564 | missense, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120560118 | AACTTCTTAGCAGAG[C/T]CAGGTTTGCTGTTAG | 8450 |
rs372966245 | snp | C/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120541139 | TATGCCACACAGCTA[C/T]CATTCTCAGGTTGAC | 8450 |
rs373274627 | snp | C/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120565401 | ACAAAACAGAAAAAA[C/T]GGCTGGGCACAGTGG | 8450 |
rs373321184 | snp | A/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120557500 | GAAATGGCAAAGTCT[A/T]CTATTAAGAAGGAGG | 8450 |
rs373326442 | snp | C/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120546899 | CAAGTGGAAATCTGA[C/T]AGGGCAAAAAGGATA | 8450 |
rs373387518 | snp | A/G | 4.58647e-05 | 0.00478855 | intron-variant | CUL4B | GRCh38.p7 | X:120535958 | TCTAAAGTAAATAAA[A/G]TAAGGCTTTATTTAA | 8450 |
rs373390962 | snp | A/G | 0.000514696 | 0.0160338 | intron-variant | CUL4B | GRCh38.p7 | X:120547088 | GTGAGGGGTAGGGAC[A/G]GAGAGGAAGACAAAA | 8450 |
rs373446197 | snp | C/G | | | downstream-variant-500B | CUL4B | GRCh38.p7 | X:120524295 | CCCCTGAACTCAAAT[C/G]TAGACTCATTTCATA | 8450 |
rs373488892 | snp | A/G | | | intron-variant | CUL4B | GRCh38.p7 | X:120575128 | CCACTTTGCTGGGTA[A/G]GATCTTCACCACAAA | 8450 |
rs373531498 | in-del | -/TTAAAA | | | intron-variant | CUL4B | GRCh38.p7 | X:120542095 | AAAAAGTTAAAAAAA[-/TTAAAA]AGAAAAAGAAAAATG | 8450 |
rs373580069 | snp | A/G | 0.000189982 | 0.00974449 | intron-variant | CUL4B | GRCh38.p7 | X:120537074 | TGAGATCTTAAAACT[A/G]CATACATTTCATATC | 8450 |
rs373582001 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120552262 | AACCGATTCTCATGC[C/T]TTAGCCTTCCCAGTA | 8450 |
rs373992272 | snp | C/T | 0.00111138 | 0.0235469 | intron-variant | CUL4B | GRCh38.p7 | X:120543867 | ATCATTCAGAAAATG[C/T]CAAGTCCAAAAGATC | 8450 |
rs373993537 | snp | G/T | 4.59021e-05 | 0.0047905 | intron-variant | CUL4B | GRCh38.p7 | X:120541755 | GGCATTAAAATATAG[G/T]GAACAAAAAAGTGAA | 8450 |
rs374060375 | snp | C/T | 0.000529661 | 0.016265 | intron-variant, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120559962 | CTCCCCTCCACCTCA[C/T]TGATTATGCATAAAA | 8450 |
rs374157027 | snp | C/T | 0.000189982 | 0.00974449 | intron-variant | CUL4B | GRCh38.p7 | X:120544453 | GATAGCAATCAGCTC[C/T]GTATAGTAGGTGTAG | 8450 |
rs374157710 | snp | C/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120537562 | CCATAATCTTACTGA[C/T]CCTGATTTTTTCTTA | 8450 |
rs374278264 | in-del | -/A | | | intron-variant | CUL4B | GRCh38.p7 | X:120547438 | CACTGTATCAAAAAA[-/A]GAACAAATTACAGGT | 8450 |
rs374381916 | snp | A/G | | | intron-variant | CUL4B | GRCh38.p7 | X:120567718 | ACCCTGTCTCTATCG[A/G]AAAAAAAAAAAAAAA | 8450 |
rs374402463 | snp | C/T | 0.000116424 | 0.00762879 | intron-variant | CUL4B | GRCh38.p7 | X:120536895 | GCTATGATTTCTATG[C/T]CTATAACTCAGTTCT | 8450 |
rs374469889 | snp | A/G | | | intron-variant | CUL4B | GRCh38.p7 | X:120534224 | AAAAAAATTTTAAAA[A/G]TTAGCCAGGCACGGT | 8450 |
rs374556865 | snp | C/G | 6.99358e-05 | 0.00591295 | missense, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120560382 | GCAGCCACTGAAACC[C/G]CCAGGCAGAAGGACG | 8450 |
rs374572926 | snp | A/G | 0.000529661 | 0.016265 | upstream-variant-2KB, intron-variant | CUL4B | GRCh38.p7 | X:120563337 | CTCCCGGGTTCAAGC[A/G]ATTCTTGTGCGTCAG | 8450 |
rs374574968 | snp | C/T | 0.018891 | 0.0953342 | intron-variant | CUL4B | GRCh38.p7 | X:120531606 | CTGGGACTACAAGCA[C/T]GCACCACCACGCCCA | 8450 |
rs374721965 | snp | C/T | 0.000542276 | 0.0164573 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120560689 | AAACCTACGTTTATA[C/T]GCCTGCGTGCGTGTA | 8450 |
rs374749433 | snp | C/T | | | upstream-variant-2KB, intron-variant | CUL4B | GRCh38.p7 | X:120562375 | GTTTTTACTTAACCT[C/T]GGGGCATTCTCAGAG | 8450 |
rs374813318 | snp | C/T | 0.000216538 | 0.010403 | intron-variant | CUL4B | GRCh38.p7 | X:120539417 | TAACCGGGGAATACA[C/T]GAGGTACTGGGCACT | 8450 |
rs374891698 | snp | C/T | 6.95491e-05 | 0.00589658 | intron-variant | CUL4B | GRCh38.p7 | X:120538082 | AAGCAGATAACTAAA[C/T]ACAACTAAGTTTGAG | 8450 |
rs374949988 | snp | A/G | | | intron-variant | CUL4B | GRCh38.p7 | X:120556176 | TATAATACGCCAAAA[A/G]AGCCATATGAAATGG | 8450 |
rs375038820 | in-del | -/G | | | intron-variant | CUL4B | GRCh38.p7 | X:120535732 | AAAAAAAAAAAAGAA[-/G]AAAACAAAAAACAAT | 8450 |
rs375313585 | snp | C/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120550674 | CAAGAAAGGCAGGAG[C/T]ATCTAAGGTGAGTTT | 8450 |
rs375364351 | snp | G/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120555601 | CTGCCAATATGTGAC[G/T]CTGGGCAGGTTATTC | 8450 |
rs375437194 | snp | A/C | | | intron-variant | CUL4B | GRCh38.p7 | X:120574105 | CCCATCACCTGCCCC[A/C]CTCTGCCCCAGCCTC | 8450 |
rs375476231 | snp | C/T | | | upstream-variant-2KB, intron-variant | CUL4B | GRCh38.p7 | X:120561360 | GGAAGCTTCGCGCCG[C/T]AGCGCCCTTACCGGA | 8450 |
rs375482997 | snp | G/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120531230 | AGGAGGCTGAGGCAG[G/T]ATAATCGCTTGAACC | 8450 |
rs375531342 | snp | C/T | 9.13638e-05 | 0.00675822 | intron-variant | CUL4B | GRCh38.p7 | X:120530275 | AAAAAAGTTTTAAAC[C/T]TAGGAATTATACCAG | 8450 |
rs375563822 | snp | A/G | | | intron-variant | CUL4B | GRCh38.p7 | X:120536456 | TTTACCAGGAGTCAG[A/G]ATAGATTTAATCAAG | 8450 |
rs375607970 | snp | C/T | 8.81679e-05 | 0.00663899 | intron-variant | CUL4B | GRCh38.p7 | X:120545435 | TTCATATTTTTCTGG[C/T]ATCCTTACCAAATGG | 8450 |
rs375681052 | snp | A/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120544301 | TGAATTTGGTTTTTA[A/T]ACATCAAGCTAGGAT | 8450 |
rs375713516 | snp | C/T | 6.29059e-05 | 0.00560794 | intron-variant, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120557921 | ATGCATATTAATACA[C/T]ACCTGGTAGAGTTCT | 8450 |
rs375822509 | snp | A/C | | | intron-variant | CUL4B | GRCh38.p7 | X:120535531 | AACATGGTGAAACCC[A/C]GTCTCCACTAAAAAT | 8450 |
rs375855167 | snp | C/T | 2.27928e-05 | 0.00337578 | intron-variant | CUL4B | GRCh38.p7 | X:120534453 | ATAGTGGTGTGCACA[C/T]AGTGAACAATTAATG | 8450 |
rs375935656 | snp | C/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120545021 | CAACTGGTTTCAATA[C/T]TGAAGAATCAGTGAA | 8450 |
rs376104143 | snp | C/G | 5.70459e-05 | 0.00534038 | intron-variant | CUL4B | GRCh38.p7 | X:120544065 | ATTCTACAAAGTAAG[C/G]TCTATTGTGAGAGAC | 8450 |
rs376135733 | snp | C/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120528613 | GTGGTCCCAGCTACT[C/T]GAGAGGCTGAGGCAA | 8450 |
rs376186212 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | CUL4B | GRCh38.p7 | X:120569517 | AGGCGCCCGCCACCA[C/T]GCCCGGCTAACTTTT | 8450 |
rs376443183 | snp | A/G | 0.00370173 | 0.0428621 | intron-variant | CUL4B | GRCh38.p7 | X:120565812 | CTCACTGCAAGCTCC[A/G]CCTCCCGGGTTCATG | 8450 |
rs376527896 | in-del | -/ATA | | | intron-variant | CUL4B | GRCh38.p7 | X:120556911 | CTCTGAAGTATATAT[-/ATA]TTTTTTTTTTTTTTT | 8450 |
rs376562806 | snp | C/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120575383 | CCCACATTCCGAAAT[C/T]TCAAAAGGGCATTTT | 8450 |
rs376566357 | snp | C/T | | | utr-variant-3-prime | CUL4B | GRCh38.p7 | X:120525325 | GGCAAGGAAATATGC[C/T]GTGGCAAAAAGCATT | 8450 |
rs376597680 | in-del | -/A | | | intron-variant | CUL4B | GRCh38.p7 | X:120556683 | TATCTCTTAAAAAAA[-/A]CAGGAAAAAAAACTG | 8450 |
rs376680956 | snp | C/G | 0.00475684 | 0.0485365 | intron-variant | CUL4B | GRCh38.p7 | X:120531083 | AATTCCAGCACTTTG[C/G]GAGGCCGAGATGGGC | 8450 |
rs376690955 | snp | A/T | 2.30468e-05 | 0.00339453 | missense, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120560330 | CTCCAGGGTGTCTTC[A/T]AAACGCAGCTTCTTC | 8450 |
rs376724471 | in-del | -/G | | | intron-variant | CUL4B | GRCh38.p7 | X:120537508 | AAAGAGGGGAAAAGG[-/G]CAAAGCAGATAAGCC | 8450 |
rs376781456 | snp | C/G | | | intron-variant | CUL4B | GRCh38.p7 | X:120540354 | AAACAACTGGAAAAA[C/G]GACTGGAAAACATAC | 8450 |
rs376833926 | snp | C/T | 0.000189982 | 0.00974449 | missense | CUL4B | GRCh38.p7 | X:120547193 | ATCTGTCTCAGCTGT[C/T]TGTACAAGTTTGCAG | 8450 |
rs376931943 | snp | A/C/G | 0.000159638 | 0.00893287 | intron-variant | CUL4B | GRCh38.p7 | X:120574505 | GCCCGGCCTGTTAAC[A/C/G]ATTATTTAGACTTAA | 8450 |
rs376966475 | snp | C/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120557303 | GTAGGGAAAAATTTC[C/T]TGGTAGCAAGGGATT | 8450 |
rs377021317 | snp | C/T | 4.77173e-05 | 0.0048843 | intron-variant | CUL4B | GRCh38.p7 | X:120537084 | AAACTGCATACATTT[C/T]ATATCATAATAACCT | 8450 |
rs377105937 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | CUL4B | GRCh38.p7 | X:120570333 | ATAAACTACAGCAGG[A/G]TTTGGAAACCACAGC | 8450 |
rs377183003 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | CUL4B | GRCh38.p7 | X:120533420 | TCCACAATCAGGCCC[C/T]ACTCATCTTACCTAA | 8450 |
rs377510489 | snp | A/G | 5.57935e-05 | 0.00528144 | intron-variant | CUL4B | GRCh38.p7 | X:120546521 | ATACAATGTTTAGCC[A/G]AAATACAATACTTTT | 8450 |
rs377572979 | snp | G/T | | | upstream-variant-2KB, utr-variant-5-prime, intron-variant | CUL4B | GRCh38.p7 | X:120561530 | ACCTTCGGAGCTCCT[G/T]ATTGGAGCTTTCTGA | 8450 |
rs377624741 | snp | C/T | 4.60299e-05 | 0.00479717 | intron-variant | CUL4B | GRCh38.p7 | X:120535975 | AAGGCTTTATTTAAG[C/T]TCTGTATCCAATACC | 8450 |
rs377668970 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | CUL4B | GRCh38.p7 | X:120548662 | AACATAGTGAAACCC[C/T]GTCTCCACTAAAAAT | 8450 |
rs377758630 | snp | A/G | 0.000347295 | 0.013173 | intron-variant | CUL4B | GRCh38.p7 | X:120537053 | TAAGAAGATCAAAAC[A/G]CACACTGAGATCTTA | 8450 |
rs398087898 | in-del | -/TT | | | intron-variant | CUL4B | GRCh38.p7 | X:120529952 | CAAAGTTTTTTTTTT[-/TT]TGGAAATCATATGCA | 8450 |
rs398122223 | in-del | -/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120529953 | AAAGTTTTTTTTTTT[-/T]GGAAATCATATGCAT | 8450 |
rs527573273 | snp | C/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120537188 | AGACTTTAAATGAAA[C/T]CTACACAAAATGCAC | 8450 |
rs528132849 | snp | A/G | | | intron-variant | CUL4B | GRCh38.p7 | X:120537309 | ACATACAGCTGGGCC[A/G]TTATAGGATCTCTTC | 8450 |
rs529033681 | snp | A/G | 0.00949095 | 0.0682305 | intron-variant | CUL4B | GRCh38.p7 | X:120557207 | TGAGCCACCGTGCCC[A/G]GCCTGAAGTATCTTT | 8450 |
rs529204224 | snp | G/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120564044 | GTGGTGGCTCATGCC[G/T]GTAATCCCAGCACTT | 8450 |
rs530346256 | snp | A/C | | | downstream-variant-500B | CUL4B | GRCh38.p7 | X:120524107 | CTCACATACACAGCA[A/C]AAATTTCAAGAGTAT | 8450 |
rs530593902 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120535011 | CTCTATTCGTAGCTC[A/C]CAGCAACAAGATTTC | 8450 |
rs530642915 | snp | A/G | 0.0026455 | 0.0362733 | intron-variant | CUL4B | GRCh38.p7 | X:120529197 | TTAAGCAGAGCATGA[A/G]GGTGAGAGGGTGGTA | 8450 |
rs531290634 | snp | C/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120529899 | ATCCAGGCTTTTCTG[C/T]TATTTTTCCCTTTTG | 8450 |
rs533223541 | snp | A/G | | | intron-variant | CUL4B | GRCh38.p7 | X:120529127 | AATATTAACTACAGC[A/G]ATCCCCTAATTTCCC | 8450 |
rs533285341 | snp | C/G | 0.00370173 | 0.0428621 | intron-variant | CUL4B | GRCh38.p7 | X:120534014 | GAGGTTGCAGTGAGC[C/G]GAGATCGCGCCACTG | 8450 |
rs533301778 | snp | C/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120548158 | GTGTACCTGTAGTTC[C/T]AGCTATTTAGGAGGC | 8450 |
rs533904228 | snp | G/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120551825 | TATGCTCTCTTACTA[G/T]TACTAAGTGCTTTCC | 8450 |
rs537274243 | in-del | -/TATATATATATATATATATATATATATATA | | | intron-variant | CUL4B | GRCh38.p7 | X:120566346 | GTGTGTGTGTATAGG[lengthTooLong]TATATATATATATAT | 8450 |
rs538289002 | snp | A/G | | | intron-variant | CUL4B | GRCh38.p7 | X:120565827 | GCCTCCCGGGTTCAT[A/G]CCATTCTCCTGCCTC | 8450 |
rs538981007 | snp | C/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120537390 | ATGTGGCTTAAACAC[C/T]TTGCAGCAACCCCCA | 8450 |
rs539651708 | snp | C/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120531320 | AGTGAGACTCCACCT[C/T]AAAAAAAAAATTTTT | 8450 |
rs539829014 | snp | C/G | | | intron-variant, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120559485 | TAGACTAGTGGTACA[C/G]AGAGTTACTACTTCT | 8450 |
rs539986416 | snp | A/G | | | intron-variant | CUL4B | GRCh38.p7 | X:120554532 | AATTACTTTAAAAAG[A/G]CAATGTTTGCTTACT | 8450 |
rs540414941 | snp | C/T | 0.0142023 | 0.083063 | utr-variant-3-prime | CUL4B | GRCh38.p7 | X:120524853 | CTCGGGGAGGGGACC[C/T]GCTTTCAAGATACTG | 8450 |
rs541008653 | snp | C/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120556047 | GATGAATCCCCTTTG[C/T]AGGCTGTCATGGACA | 8450 |
rs544263482 | snp | A/G | | | upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120577012 | CTAGAAGCAGAGAGG[A/G]AGGAATGCTGGGCAA | 8450 |
rs547444008 | snp | C/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120567024 | TTCTGTTTACTTTAT[C/T]GATGTCTCTCAAAGT | 8450 |
rs547671560 | snp | C/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120537356 | ATACCACCTGCAGTC[C/T]CCACCTTTGAATACC | 8450 |
rs547892242 | snp | A/G | | | intron-variant | CUL4B | GRCh38.p7 | X:120530472 | AATGAAGTAATGCTA[A/G]TATTAGTTAATAGAA | 8450 |
rs548846676 | snp | C/T | | | upstream-variant-2KB, utr-variant-5-prime, intron-variant | CUL4B | GRCh38.p7 | X:120561468 | GGGGGGAGGGAGAAA[C/T]TGGGGGGAAGAAAAG | 8450 |
rs549182428 | snp | A/C | | | intron-variant | CUL4B | GRCh38.p7 | X:120557411 | AAGCTGCTGGACTAC[A/C]AACTGCTACTCATTT | 8450 |
rs549850118 | snp | A/G | | | intron-variant | CUL4B | GRCh38.p7 | X:120557131 | GGTCAGGCTGGTCTC[A/G]AACTCCTGACCTCAG | 8450 |
rs549882889 | snp | A/G | | | upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120576609 | CTAGGCTCTCACTCC[A/G]TCTCATCTTTCATCT | 8450 |
rs550310351 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120555052 | TAGCAAAAGCAGTAA[A/G]GTATTATGAAAAATG | 8450 |
rs552744238 | snp | A/G | 0.0168099 | 0.0901243 | intron-variant | CUL4B | GRCh38.p7 | X:120564492 | GTGCCTGTAATCCCA[A/G]CTACTCGGGAGGATA | 8450 |
rs554439784 | snp | A/G | | | intron-variant | CUL4B | GRCh38.p7 | X:120569545 | TTTTATATTTTTAGT[A/G]GAGACGGGGTTTCAC | 8450 |
rs554702347 | snp | A/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120533665 | TGCCAGTCCACGGTG[A/T]TCTCTTGCTTTGTTG | 8450 |
rs554947816 | snp | A/G | | | intron-variant | CUL4B | GRCh38.p7 | X:120541507 | TCTGTCTCAAAAAAA[A/G]AAAAATTGGATCAAA | 8450 |
rs556028573 | snp | A/G | | | upstream-variant-2KB, intron-variant | CUL4B | GRCh38.p7 | X:120562680 | CAAAAAGAGAAGAGG[A/G]AACAGGATGAAAGGC | 8450 |
rs556531012 | snp | C/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120559627 | ATCTAATTATAAATC[C/T]TATTTGAGCATAAAA | 8450 |
rs557842677 | snp | G/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120571510 | AATGGACTCTCTATG[G/T]TCCACAATATGGGGG | 8450 |
rs558287234 | snp | C/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120572261 | TTGAAGTCAGGAGTT[C/T]AAGACCAGCCTGACC | 8450 |
rs558960054 | snp | A/G | 0.00422943 | 0.0457911 | intron-variant | CUL4B | GRCh38.p7 | X:120531553 | CAACCTCCACATCCC[A/G]GGTTCAGGTGATTCT | 8450 |
rs559169390 | snp | A/G | | | intron-variant | CUL4B | GRCh38.p7 | X:120564671 | AAGAACCAACTAATT[A/G]AGGCTAGTTGAAGAA | 8450 |
rs560714983 | in-del | -/AT | | | intron-variant | CUL4B | GRCh38.p7 | X:120556913 | CTGAAGTATATATAT[-/AT]TTTTTTTTTTTTTTG | 8450 |
rs560784961 | snp | G/T | 0.0194105 | 0.0965841 | intron-variant | CUL4B | GRCh38.p7 | X:120554121 | TTTAAAATAAAGATT[G/T]CTTTTCTAAAGACTC | 8450 |
rs561089327 | snp | A/G | | | intron-variant | CUL4B | GRCh38.p7 | X:120540153 | TAAATAGTGTCCAAC[A/G]TACTGTCTTTGAAAG | 8450 |
rs563431672 | snp | A/G | 0.00211696 | 0.0324653 | intron-variant | CUL4B | GRCh38.p7 | X:120539040 | GTAGCTTTGGTGCCA[A/G]TATTTAAGAGATTAA | 8450 |
rs563610680 | snp | A/C | | | intron-variant | CUL4B | GRCh38.p7 | X:120557142 | TCTCGAACTCCTGAC[A/C]TCAGGTGATCTGCCA | 8450 |
rs564101127 | snp | C/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120556762 | AACTAGATCCCAAAC[C/T]CATCTTCTGACTCCT | 8450 |
rs564389017 | snp | A/G | | | intron-variant | CUL4B | GRCh38.p7 | X:120575203 | AGGTGAATAAAGGCT[A/G]TAACTTTTAACATAC | 8450 |
rs564567505 | snp | A/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120540725 | CCAGGCTAGTCTGAA[A/T]CTCCTAGGCTGAAAG | 8450 |
rs567034114 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120545256 | ATATATGCCCAGGGA[A/C]TGTTAGCTATCTTCA | 8450 |
rs567282410 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120529372 | GGTAAGTACTATTAT[C/T]ATCTCAGTTTTACAA | 8450 |
rs568008885 | snp | A/G | | | intron-variant | CUL4B | GRCh38.p7 | X:120536764 | ACTTCGGAAGGCTGA[A/G]GCGGGGGGGATCACT | 8450 |
rs569462458 | snp | C/T | 0.00791544 | 0.0624105 | intron-variant | CUL4B | GRCh38.p7 | X:120542501 | GGGATTAGAAGTGCT[C/T]GGTTTGACATGCCAT | 8450 |
rs569743213 | snp | A/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120526991 | ATTTTTATTTATTTA[A/T]ATCTCTTTTTTAGAG | 8450 |
rs570082579 | snp | A/G | | | upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120576954 | GGACTATATTGAAAG[A/G]ATAAAGTAGGAGCAG | 8450 |
rs571616116 | snp | C/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120529383 | TTATTATCTCAGTTT[C/T]ACAAAAGAGGAAACA | 8450 |
rs573232206 | snp | C/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120531441 | CAAAAACAAACAAAA[C/T]ATTCACCTTCCCTGT | 8450 |
rs573519491 | snp | A/T | 0.00422943 | 0.0457911 | intron-variant | CUL4B | GRCh38.p7 | X:120527695 | TACCTTTTGTGCATG[A/T]AACAAAGTTTTGACT | 8450 |
rs574535531 | snp | C/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120541810 | AATTTGAGTTATAAT[C/T]ATTATTGTGATACTG | 8450 |
rs574761512 | snp | G/T | 0.00475684 | 0.0485365 | intron-variant | CUL4B | GRCh38.p7 | X:120567297 | CCCAGCTAAATTTTT[G/T]GGTATTTTTAGTAGA | 8450 |
rs575452220 | snp | C/T | 0.00422943 | 0.0457911 | intron-variant | CUL4B | GRCh38.p7 | X:120550919 | AAAAACATACACAGT[C/T]GTTTTACGTATATAA | 8450 |
rs575733603 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120530542 | GCTGATGTGGAATTT[A/T]CCATTTTGTTTTTTT | 8450 |
rs577098918 | snp | C/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120552390 | TGACCTCAGGTGATC[C/T]GCCCACCTTGGCCTC | 8450 |
rs577140757 | snp | C/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120543422 | AGAAATAGGGGAATC[C/T]ACTGAATTTTAATTG | 8450 |
rs577291875 | snp | A/C | | | intron-variant | CUL4B | GRCh38.p7 | X:120538260 | AGTGGTAAAAACAAA[A/C]GAGGTTTAAAAGTGG | 8450 |
rs577354048 | snp | A/G | | | intron-variant | CUL4B | GRCh38.p7 | X:120546113 | GGTAAGTGTGACAAA[A/G]ATAAAAATGAACCTA | 8450 |
rs577690680 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120571808 | AATCAAGCAGGAATG[A/G]AAAATACAGGATTTG | 8450 |
rs577862688 | snp | A/G | | | intron-variant | CUL4B | GRCh38.p7 | X:120528646 | GAATTGCTTGAACCC[A/G]GGAGGCAGACGCTGC | 8450 |
rs745311111 | snp | C/T | 1.75971e-05 | 0.00296618 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | CUL4B | GRCh38.p7 | X:120561436 | CCAGGTCCGCAGGAC[C/T]TGAGTGGGGGGGGGA | 8450 |
rs745313145 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120528934 | CTAGTCTGTAAATAT[A/G]ATATAATCTTGTTTG | 8450 |
rs745332228 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | CUL4B | GRCh38.p7 | X:120539140 | TCACGTATCCCCCCA[A/G]TGAATTAAACACAAT | 8450 |
rs745373947 | in-del | -/AAAAAAAAAAAA | | | intron-variant | CUL4B | GRCh38.p7 | X:120535704 | GTGAGACTCTGTCTC[-/AAAAAAAAAAAA]AAAAAAAAAAAAAAA | 8450 |
rs745386257 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120572656 | GCAGTTTTTGCTTTT[C/T]TTAAAAAAAGGATCA | 8450 |
rs745410440 | snp | A/C | | | downstream-variant-500B | CUL4B | GRCh38.p7 | X:120524091 | TTTTCTGAACTGTAC[A/C]CTCACATACACAGCA | 8450 |
rs745426768 | snp | A/C | 2.30843e-05 | 0.0033973 | intron-variant | CUL4B | GRCh38.p7 | X:120538100 | AACTAAGTTTGAGGA[A/C]TTAAGAGTTTAACTC | 8450 |
rs745447566 | snp | G/T | | | intron-variant, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120558224 | TTTGAAATGCCATAA[G/T]ACTGTTTAAGTCATT | 8450 |
rs745489781 | in-del | -/AA | | | intron-variant | CUL4B | GRCh38.p7 | X:120555160 | CAAGAAAACAAAAAC[-/AA]GAGATGCAAGCTCTA | 8450 |
rs745496294 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120571688 | TAGGCAACTGTTTAC[A/T]GGTGACCCTTGAACA | 8450 |
rs745525325 | snp | C/T | 0.000529661 | 0.016265 | downstream-variant-500B | CUL4B | GRCh38.p7 | X:120524098 | AACTGTACACTCACA[C/T]ACACAGCAAAAATTT | 8450 |
rs745527214 | snp | C/T | 0.000205196 | 0.010127 | intron-variant | CUL4B | GRCh38.p7 | X:120574524 | ATTTAGACTTAACTC[C/T]TGAGTTTTACTAGTT | 8450 |
rs745587992 | snp | A/T | 0.00370173 | 0.0428621 | intron-variant | CUL4B | GRCh38.p7 | X:120545701 | TTACTCAACAGTCAA[A/T]CCTTTTTGTGTTTTC | 8450 |
rs745615241 | snp | C/G | 2.28297e-05 | 0.00337851 | utr-variant-3-prime | CUL4B | GRCh38.p7 | X:120526747 | ATGACACCAAATGCT[C/G]CAAGGCCAACATTCT | 8450 |
rs745714536 | snp | A/G | | | upstream-variant-2KB, intron-variant | CUL4B | GRCh38.p7 | X:120562409 | GGTAACACAATATCA[A/G]AAACTAAATTTGCCA | 8450 |
rs745717317 | snp | A/G | | | intron-variant | CUL4B | GRCh38.p7 | X:120537080 | CTTAAAACTGCATAC[A/G]TTTCATATCATAATA | 8450 |
rs745795724 | in-del | -/G | 7.83853e-05 | 0.00625991 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | CUL4B | GRCh38.p7 | X:120561439 | GTCCGCAGGACTTGA[-/G]GTGGGGGGGGGAAGG | 8450 |
rs745809804 | snp | A/C | 2.28217e-05 | 0.00337792 | intron-variant | CUL4B | GRCh38.p7 | X:120530264 | TTCAACCTAACAAAA[A/C]AGTTTTAAACCTAGG | 8450 |
rs745846568 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120554405 | AATTAAAAACAAGCA[C/T]GCAAACAAACAAAAC | 8450 |
rs745852631 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120565631 | AGGTTGCAGTGAGCC[A/G]AGATTGCACCACTGC | 8450 |
rs745878053 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120552495 | TTTAAGCTCCCACTA[A/G]TTACCAGTAAATATG | 8450 |
rs745906391 | snp | C/G | 2.28074e-05 | 0.00337686 | intron-variant | CUL4B | GRCh38.p7 | X:120541571 | GTAGATAAGCCATAA[C/G]AGAGAAAAATCACAG | 8450 |
rs745916925 | snp | C/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120573041 | TAGAAGAATATAGGA[C/T]AAAAAGTGTAAGTGT | 8450 |
rs745930328 | snp | G/T | 0.000529661 | 0.016265 | upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120576421 | GAAAAAAATGGAAAT[G/T]ATGGGATTCTATATA | 8450 |
rs745995079 | snp | A/G | 2.389e-05 | 0.00345607 | intron-variant | CUL4B | GRCh38.p7 | X:120540349 | TCATTAAACAACTGG[A/G]AAAAGGACTGGAAAA | 8450 |
rs746008855 | snp | A/G | 2.71109e-05 | 0.00368167 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120560645 | TGGAAACATGAAAAT[A/G]GCGGGGTCAACAGGC | 8450 |
rs746031320 | snp | C/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120575147 | CTTCACCACAAATAA[C/T]TATGACTCTAACGAG | 8450 |
rs746123594 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | CUL4B | GRCh38.p7 | X:120550462 | TAAGCAGAGAGATGA[A/G]GCCCCTAACCCAGCA | 8450 |
rs746126820 | snp | A/G | | | intron-variant | CUL4B | GRCh38.p7 | X:120530603 | TGTATCAGTTTCAAT[A/G]GATTGTTAACCAGAT | 8450 |
rs746140557 | snp | C/T | 0.000529661 | 0.016265 | upstream-variant-2KB, intron-variant | CUL4B | GRCh38.p7 | X:120562632 | GAGTTCTACAGAGAT[C/T]ATGTTTATGCTGTGT | 8450 |
rs746161299 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | CUL4B | GRCh38.p7 | X:120547638 | CTAGAACAGCCTAGG[C/T]AACTGTGATGGTTAC | 8450 |
rs746179024 | snp | A/T | 0.000529661 | 0.016265 | intron-variant, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120559206 | CTTCTCTATTTAATA[A/T]ACACTGTAGCACTGA | 8450 |
rs746243519 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120557729 | CAAATATAAGCACAA[C/T]TTATACTGGTATGAC | 8450 |
rs746267103 | snp | A/G | 0.00211696 | 0.0324653 | intron-variant | CUL4B | GRCh38.p7 | X:120567763 | CTGGCATATCCCAGC[A/G]CTTTGGGATGCTGAG | 8450 |
rs746272874 | snp | A/G | | | intron-variant | CUL4B | GRCh38.p7 | X:120532061 | TTATTTATAATACTA[A/G]TAAGTCATGAATTTA | 8450 |
rs746406855 | in-del | -/T | 0.499962 | 0.00437069 | intron-variant | CUL4B | GRCh38.p7 | X:120567119 | CAAGGCCAATTTAGA[-/T]TTTTTTTTTTTTTTT | 8450 |
rs746427421 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120543159 | AGATTCCTATCCTAT[A/G]TATAAATTTATTGGT | 8450 |
rs746547887 | snp | C/T | 2.34176e-05 | 0.00342173 | synonymous-codon | CUL4B | GRCh38.p7 | X:120547153 | TCTGAATTGATGAAT[C/T]TGTGCTTTGATGTGA | 8450 |
rs746635504 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120530049 | TGTCTGAAAATCTAA[C/T]GTACTTTCTTTTATT | 8450 |
rs746682739 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120573890 | GTGCAATGGCACAAT[A/C]TCTGCTCACTGCAAG | 8450 |
rs746690704 | in-del | -/AGC | 5.47241e-05 | 0.00523059 | cds-indel, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120560588 | AGATCTGACCTCCTG[-/AGC]AGCAGCAGCAGCTGA | 8450 |
rs746716788 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120564961 | GAAGTGTAGTTATTA[C/T]TGGCCACCTTTAACC | 8450 |
rs746726033 | snp | C/T | 6.84221e-05 | 0.00584862 | intron-variant | CUL4B | GRCh38.p7 | X:120535782 | GAAGGATGACCTAAA[C/T]ATTAAAGATAAAGAT | 8450 |
rs746763400 | snp | A/G | 3.24438e-05 | 0.00402751 | intron-variant | CUL4B | GRCh38.p7 | X:120543069 | GTTAGTATTATTGAC[A/G]TTTGACTTCCAGAAA | 8450 |
rs746823585 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120569639 | TGCTGGGATTACAGG[C/T]GTGAGCCACCGCGCC | 8450 |
rs746853290 | snp | C/G | 6.94011e-05 | 0.00589031 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | CUL4B | GRCh38.p7 | X:120561422 | AGATCCCGAAGCCCC[C/G]AGGTCCGCAGGACTT | 8450 |
rs746854249 | in-del | -/AA | 0.0107579 | 0.0725481 | intron-variant | CUL4B | GRCh38.p7 | X:120543042 | TGACTTCCTACAAGG[-/AA]AAAAAAAAAGGTTAG | 8450 |
rs746867066 | snp | G/T | | | intron-variant, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120559487 | GACTAGTGGTACACA[G/T]AGTTACTACTTCTGT | 8450 |
rs746888483 | snp | C/T | | | intron-variant, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120557760 | TGTACCCATGGTTTA[C/T]GTGAGAATACGTGGT | 8450 |
rs746895126 | snp | G/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120534724 | CAAAGCCACTTGACG[G/T]GGTAATACAGTATTT | 8450 |
rs746945066 | snp | C/G | 2.81061e-05 | 0.00374863 | intron-variant | CUL4B | GRCh38.p7 | X:120544080 | GTCTATTGTGAGAGA[C/G]AGTGAGAATTTATTA | 8450 |
rs746980344 | snp | A/G | | | synonymous-codon | CUL4B | GRCh38.p7 | X:120536957 | AACTTCCATAGGCAC[A/G]TATGTCGGCCAATAG | 8450 |
rs746992171 | snp | C/G | 0.00370173 | 0.0428621 | intron-variant | CUL4B | GRCh38.p7 | X:120556598 | TAATCTCAGCACCTT[C/G]GGAGGTTGAGGTGAC | 8450 |
rs746998481 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120545804 | ATATAATTCTTCCTG[A/C]GCCACAGTGCTAGGG | 8450 |
rs747009331 | in-del | -/ATT | | | intron-variant | CUL4B | GRCh38.p7 | X:120556913 | CTGAAGTATATATAT[-/ATT]TTTTTTTTTTTTTGA | 8450 |
rs747039580 | snp | A/G | 4.95866e-05 | 0.00497904 | intron-variant | CUL4B | GRCh38.p7 | X:120538807 | ATTTATAATATTCCA[A/G]TAAAAAGTACTGACA | 8450 |
rs747056505 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120533326 | TTGATTTCAGTAAGT[A/G]GTCCAAATAATTACT | 8450 |
rs747100648 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120567176 | TCGCCCAGGCTGGAG[G/T]GCAGTGGTGCAATGT | 8450 |
rs747113710 | snp | A/G | | | intron-variant | CUL4B | GRCh38.p7 | X:120546033 | GGATAATCATCAAGA[A/G]AGAAAAAAAAATAAG | 8450 |
rs747127577 | snp | C/G | 2.27988e-05 | 0.00337622 | missense, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120560236 | TAAGTTGCTGCTGCT[C/G]AGATGTTGCAGCAGT | 8450 |
rs747128099 | snp | G/T | 0.00158814 | 0.0281345 | upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120577341 | GGTGTGGTGGCTCAT[G/T]TCTGTAATTCCAGCG | 8450 |
rs747198401 | snp | A/G | 0.000529661 | 0.016265 | upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120576481 | TCTTGTTTGCAAGTG[A/G]CAGAAACCCAACTTG | 8450 |
rs747220282 | snp | C/G | | | intron-variant | CUL4B | GRCh38.p7 | X:120549986 | TCCTTCTGCTATGTT[C/G]CCTTCTCAAATAAAA | 8450 |
rs747233628 | snp | A/C | 1.69117e-05 | 0.00290785 | intron-variant | CUL4B | GRCh38.p7 | X:120539424 | GGAATACACGAGGTA[A/C]TGGGCACTATATATA | 8450 |
rs747241249 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120528614 | TGGTCCCAGCTACTC[A/G]AGAGGCTGAGGCAAA | 8450 |
rs747332350 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | CUL4B | GRCh38.p7 | X:120549291 | GAGCGCGGTGGCTCA[C/T]GCCTGTAATCCCAGC | 8450 |
rs747377842 | snp | A/G | | | intron-variant | CUL4B | GRCh38.p7 | X:120527881 | TTGTCATATTGTTAC[A/G]GAATACTTTCTATTA | 8450 |
rs747399004 | snp | A/C | 2.72331e-05 | 0.00368996 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120560655 | AAAATAGCGGGGTCA[A/C]CAGGCAGAGGAGCAT | 8450 |
rs747451755 | snp | C/T | 0.000529661 | 0.016265 | downstream-variant-500B | CUL4B | GRCh38.p7 | X:120524130 | AAGAGTATGGCTAGA[C/T]ATCATATTAAGACCA | 8450 |
rs747462675 | in-del | -/A | | | intron-variant | CUL4B | GRCh38.p7 | X:120567872 | AGTAAGACTCTGAAG[-/A]AAAAAAAAAAAAAAC | 8450 |
rs747542233 | snp | A/G | | | intron-variant | CUL4B | GRCh38.p7 | X:120529812 | GTAAATAACCAACCA[A/G]GAAGTTCAAAAGAAA | 8450 |
rs747542578 | snp | C/G | 2.58742e-05 | 0.00359673 | missense | CUL4B | GRCh38.p7 | X:120546597 | TCTTCTTTAAAAAAA[C/G]AACGCTATCCAATGA | 8450 |
rs747556464 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120568661 | CAAAATTCAATTTGT[A/G]GTTGATTTCACAGTT | 8450 |
rs747620437 | snp | A/G | 2.53065e-05 | 0.00355705 | synonymous-codon | CUL4B | GRCh38.p7 | X:120546580 | TTGCCAGCATCTATC[A/G]ATCTTCTTTAAAAAA | 8450 |
rs747620876 | snp | A/C | 3.29462e-05 | 0.00405857 | synonymous-codon | CUL4B | GRCh38.p7 | X:120532461 | GATCTTTATCCTGAA[A/C]AGTTTATGTTTGAAA | 8450 |
rs747635585 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | CUL4B | GRCh38.p7 | X:120556705 | AAAAAACTGAGAGGG[C/T]TTTAGTACCTGGCCC | 8450 |
rs747671064 | snp | C/T | | | upstream-variant-2KB, intron-variant | CUL4B | GRCh38.p7 | X:120562767 | TGGAAACATGGAAAG[C/T]GCAGTGAGGCTGGGA | 8450 |
rs747680906 | snp | C/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120564028 | ACAGATCTGGCCACG[C/T]GTGGTGGCTCATGCC | 8450 |
rs747725215 | snp | C/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120539849 | TACATAGTAGATAGG[C/T]TGCAACAAAATTTCA | 8450 |
rs747747919 | snp | C/G | | | intron-variant | CUL4B | GRCh38.p7 | X:120542415 | GAAAATATTATTGGG[C/G]AGAAAGGTAAGGCTT | 8450 |
rs747816205 | snp | A/T | 0.000159522 | 0.00892949 | intron-variant | CUL4B | GRCh38.p7 | X:120534477 | ATTAATGTTTGCTAC[A/T]AACCTATTCCAGTTG | 8450 |
rs747821941 | in-del | -/CAT | 4.84754e-05 | 0.00492294 | intron-variant | CUL4B | GRCh38.p7 | X:120540332 | TTATGACTCAAAGAA[-/CAT]CATTAAACAACTGGA | 8450 |
rs747875273 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120555864 | AGAGGATCACTTGAG[C/G]CCGGGAGGTGGAGGT | 8450 |
rs747903258 | snp | A/G | 0.00422943 | 0.0457911 | intron-variant | CUL4B | GRCh38.p7 | X:120527868 | AACTGTCACATCCTT[A/G]TCATATTGTTACGGA | 8450 |
rs747903593 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120531066 | CAGTGGCTCACACCT[A/G]TAATTCCAGCACTTT | 8450 |
rs747908722 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120571483 | GGGATGCACCCTCCA[A/G]CCTGGTGGAAGAATG | 8450 |
rs747933190 | in-del | -/TATG | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120552034 | TATTCTTTTAAATAT[-/TATG]TATTTATTATTTATG | 8450 |
rs747988009 | snp | C/T | 0.000529661 | 0.016265 | upstream-variant-2KB, intron-variant | CUL4B | GRCh38.p7 | X:120562869 | AGTCTACTCTGTAGG[C/T]GATCATAGATAGCAG | 8450 |
rs747997744 | snp | A/G | 2.33084e-05 | 0.00341374 | missense, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120560415 | GTTGAAGGGGATGCC[A/G]AATCCCTGGGTTGTA | 8450 |
rs748010886 | snp | C/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120556228 | TAGTACTACAACTAC[C/T]AGCCGACATTTGCAT | 8450 |
rs748040218 | snp | C/T | 2.27951e-05 | 0.00337595 | missense | CUL4B | GRCh38.p7 | X:120541669 | CTACTGAAGAGCTGA[C/T]ACAGAAGAGACAAAT | 8450 |
rs748079956 | snp | C/T | | | synonymous-codon | CUL4B | GRCh38.p7 | X:120530207 | AGCATCAATTTGATA[C/T]TGTCTGTCTTGAAAT | 8450 |
rs748103861 | snp | C/T | 3.47881e-05 | 0.00417047 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | CUL4B | GRCh38.p7 | X:120561413 | ATAGCGCCCAGATCC[C/T]GAAGCCCCCAGGTCC | 8450 |
rs748104983 | snp | C/G | | | intron-variant | CUL4B | GRCh38.p7 | X:120557461 | GTAGCCCAGGTATTA[C/G]AAAAATGTAAAGAGC | 8450 |
rs748174699 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120534877 | CATTCTAGATATTCA[C/T]CACAAGCAGCAAGAA | 8450 |
rs748210847 | snp | C/G | 0.000529661 | 0.016265 | downstream-variant-500B | CUL4B | GRCh38.p7 | X:120524259 | GAGCAAATGCCATAA[C/G]TAAGAGTAATCTTTT | 8450 |
rs748212974 | snp | C/G | 1.65941e-05 | 0.00288041 | intron-variant, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120558087 | ACCATGTCAGATACA[C/G]TAACCAAAGATTCAT | 8450 |
rs748231013 | in-del | -/A | 0.00105904 | 0.0229869 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120560760 | AGAGAGGAGAAACAC[-/A]AGAGGACGAGAAGGA | 8450 |
rs748277464 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120567992 | TAAGCACTTGTATTC[C/T]GTTTAATGCCTGAAA | 8450 |
rs748316891 | snp | A/G | 2.28561e-05 | 0.00338046 | utr-variant-3-prime | CUL4B | GRCh38.p7 | X:120526721 | GTTAGTTTATCCACT[A/G]GCTACTGCATATGAC | 8450 |
rs748328122 | snp | A/G | 4.55814e-05 | 0.00477375 | missense, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120560143 | TGTTAGCAAAGCTAG[A/G]GACGGTGGTAGAAGA | 8450 |
rs748410967 | snp | C/T | 0.000146265 | 0.0085505 | intron-variant | CUL4B | GRCh38.p7 | X:120538228 | TTAAAGATGTTTGTA[C/T]ATGTATAATATTTTA | 8450 |
rs748430150 | in-del | -/ATCAGCTCTGT | 0.00112526 | 0.0236931 | intron-variant | CUL4B | GRCh38.p7 | X:120544444 | AAAACTAGGATAGCA[-/ATCAGCTCTGT]ATCAGCTCTGTATAG | 8450 |
rs748441588 | in-del | -/T | | | utr-variant-3-prime | CUL4B | GRCh38.p7 | X:120525369 | TTTAACAAACATAAA[-/T]CAAAATTTTCTGCTT | 8450 |
rs748497791 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120539635 | TGATGTTTATGAAAA[C/T]AGGATACGGATATCC | 8450 |
rs748499378 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120565848 | CTCCTGCCTCAGCCT[C/T]CCAAGTAGCTGGGAC | 8450 |
rs748515783 | snp | C/G | 0 | 0 | intron-variant | CUL4B | GRCh38.p7 | X:120574104 | CCCCATCACCTGCCC[C/G]CCTCTGCCCCAGCCT | 8450 |
rs748522493 | snp | A/T | 1.64857e-05 | 0.00287099 | intron-variant | CUL4B | GRCh38.p7 | X:120538781 | CTTGCCTATGTAAAA[A/T]GAAATGCAAAATTTA | 8450 |
rs748526849 | snp | C/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120548535 | AAGAATAGTTAAATA[C/T]AGATTTTAAAATCTG | 8450 |
rs748558022 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120550299 | ATAAGTTCTTTAATA[C/T]TTTTTGAGCTTTGAA | 8450 |
rs748591748 | snp | C/T | | | downstream-variant-500B | CUL4B | GRCh38.p7 | X:120524462 | ATACTCTTATAGCAT[C/T]ACCACAAAACCATTA | 8450 |
rs748606537 | snp | A/T | 0.000529661 | 0.016265 | utr-variant-3-prime | CUL4B | GRCh38.p7 | X:120525844 | AAAACTGTCCAAACA[A/T]CATTTAAAGTCTAAA | 8450 |
rs748629805 | snp | A/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120549856 | TTCCTTCTGAATGAC[A/T]GTTTTCTCAGCATTT | 8450 |
rs748686097 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120537455 | TTTCACTTGCTCCAC[A/T]GCCTGTCTGCAGGGA | 8450 |
rs748696316 | snp | C/G | 2.41949e-05 | 0.00347806 | missense | CUL4B | GRCh38.p7 | X:120544182 | CTTCCAAAAATCGTT[C/G]TTCAAAAGAATCTTG | 8450 |
rs748711131 | in-del | -/CTCC | 0.0017685 | 0.0296837 | upstream-variant-2KB, intron-variant | CUL4B | GRCh38.p7 | X:120561323 | CACCGGGAACTCCCA[-/CTCC]CTCCTTAACGGTCCC | 8450 |
rs748717294 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120549381 | ACATAGTGAAACCCT[C/G]TCTCTACTAAAAATA | 8450 |
rs748734468 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120548386 | AGATGGGTTGGGCAG[C/T]CCTACTACAATTGAA | 8450 |
rs748776087 | in-del | -/A | 0.00105904 | 0.0229869 | intron-variant | CUL4B | GRCh38.p7 | X:120547432 | CCAATGCACTGTATC[-/A]AAAAAAGAACAAATT | 8450 |
rs748785719 | in-del | -/ACACACA | | | intron-variant | CUL4B | GRCh38.p7 | X:120543524 | CACACACACACACAC[-/ACACACA]CACCCCTAATAATCG | 8450 |
rs748790733 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120571601 | CAGTGAGATCTAGAG[A/C]TCTATGGATTACTTG | 8450 |
rs748811295 | snp | G/T | 0.00475684 | 0.0485365 | intron-variant | CUL4B | GRCh38.p7 | X:120571043 | AGGGGGTGGGGTGGG[G/T]TGGGGGGAATAATTA | 8450 |
rs748862119 | snp | C/T | | | intron-variant, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120560027 | CATAAATAGAGCACG[C/T]GACCCCTCGAGTGTC | 8450 |
rs748882631 | snp | A/G | | | upstream-variant-2KB, intron-variant | CUL4B | GRCh38.p7 | X:120562658 | TGTGTCTCAAAGTGG[A/G]AGTTGCCAAAAAGAG | 8450 |
rs748894655 | snp | A/G | 2.28172e-05 | 0.00337759 | synonymous-codon | CUL4B | GRCh38.p7 | X:120526767 | GCCAACATTCTATGC[A/G]ATATAGTTGTACTGG | 8450 |
rs748966670 | snp | C/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120539702 | ATGTAATCCAAGCCA[C/T]GAAAAGACATGAGGA | 8450 |
rs748972529 | in-del | -/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120567485 | AGAATGACCTAGGAG[-/T]TTTTTTTGTTTTTTA | 8450 |
rs749011098 | in-del | -/A | 0.0152462 | 0.0859689 | upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120577444 | CTCTACAAAGAATAC[-/A]AAAAATTAGCTGGGT | 8450 |
rs749131350 | snp | C/T | | | synonymous-codon | CUL4B | GRCh38.p7 | X:120541653 | AACTCCACCTCGAAC[C/T]CTACTGAAGAGCTGA | 8450 |
rs749133630 | in-del | -/A | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120552913 | CTCTCTTTTTATGTC[-/A]AGTAAATATGGCTAA | 8450 |
rs749167962 | snp | C/G | 2.28574e-05 | 0.00338056 | intron-variant | CUL4B | GRCh38.p7 | X:120530290 | CTAGGAATTATACCA[C/G]AAGCAAAACCTGACT | 8450 |
rs749176803 | snp | A/G | 0.000209834 | 0.0102408 | missense, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120560391 | GAAACCCCCAGGCAG[A/G]AGGACGAGGTTGAAG | 8450 |
rs749216323 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120528707 | GCCTGGATGACAGAG[C/T]GAGACTCCATCTCAA | 8450 |
rs749303244 | snp | A/C | | | intron-variant | CUL4B | GRCh38.p7 | X:120552856 | AAGTAAAGCACATAA[A/C]AAAAAATTCAACAAC | 8450 |
rs749304213 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120528055 | AAGCACACCTTTACT[G/T]TGGGCAAGAGTTAGT | 8450 |
rs749311084 | snp | G/T | 0.000529661 | 0.016265 | missense | CUL4B | GRCh38.p7 | X:120538126 | AACTCACTTTTACCT[G/T]TTTGAACTGAATCAT | 8450 |
rs749324294 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120526954 | ACAGTTTCGGCTCAT[G/T]AATTTAATCTCCTTT | 8450 |
rs749346111 | snp | A/G | | | upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120577329 | CTTTTCTAGCTGGGT[A/G]TGGTGGCTCATGTCT | 8450 |
rs749412282 | snp | G/T | 0.00855599 | 0.0648444 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | CUL4B | GRCh38.p7 | X:120561441 | TCCGCAGGACTTGAG[G/T]GGGGGGGGGAAGGGG | 8450 |
rs749443971 | snp | C/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120531098 | GGAGGCCGAGATGGG[C/T]GGATCATGAGGTCAG | 8450 |
rs749446807 | snp | A/G | 2.61534e-05 | 0.00361607 | intron-variant | CUL4B | GRCh38.p7 | X:120543039 | TAATGACTTCCTACA[A/G]GGAAAAAAAAAAAGG | 8450 |
rs749448843 | snp | A/C | | | intron-variant | CUL4B | GRCh38.p7 | X:120556025 | ATGCTTATATGAGAT[A/C]ATACGAGATGAATCC | 8450 |
rs749467601 | snp | A/C | | | intron-variant | CUL4B | GRCh38.p7 | X:120532206 | AATACTAAATAAACA[A/C]AGTAAGATATGAAAC | 8450 |
rs749492263 | in-del | -/AAAAAAAAAAAAAAAAAAAAAAAAAAAAACCCAAAAAAAAA | | | intron-variant | CUL4B | GRCh38.p7 | X:120572472 | ACTCCTCAAAAAAAA[lengthTooLong]AAAAAAAAAAAGAAA | 8450 |
rs749500198 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | CUL4B | GRCh38.p7 | X:120535646 | AGGAGGCAGAGGTTG[C/T]GGTGAGCCAAGATAG | 8450 |
rs749508691 | snp | G/T | 0.000529661 | 0.016265 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120560789 | GAAAGTGAAGGGGGG[G/T]GCTACACCGGGGGAA | 8450 |
rs749512243 | in-del | -/CCTTCTAAACAC | | | intron-variant | CUL4B | GRCh38.p7 | X:120543488 | ATTATTTCTAAATTA[-/CCTTCTAAACAC]ACACACACACACACA | 8450 |
rs749522507 | snp | A/T | 2.93975e-05 | 0.00383378 | intron-variant | CUL4B | GRCh38.p7 | X:120547279 | AGGAGAGGATGAAGG[A/T]TTTCTCAACTATTTA | 8450 |
rs749620514 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120531849 | ATATAATCTTTAGTG[C/T]TGGGGGACATAGTAA | 8450 |
rs749631148 | snp | A/G | 6.87892e-05 | 0.00586429 | synonymous-codon | CUL4B | GRCh38.p7 | X:120538163 | TTTAGAAAGTTCCAT[A/G]TCTTTAAACATTCCT | 8450 |
rs749661317 | snp | A/T | 0.00370173 | 0.0428621 | intron-variant | CUL4B | GRCh38.p7 | X:120566380 | ATATATATATATATA[A/T]ATATATATATGTATA | 8450 |
rs749664158 | snp | C/T | 0.000310781 | 0.0124617 | intron-variant, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120558076 | GGCATCAGAATACCA[C/T]GTCAGATACAGTAAC | 8450 |
rs749716931 | in-del | -/TTCAACCGATT | | | intron-variant | CUL4B | GRCh38.p7 | X:120552243 | CCTCTGCCTCCTGGG[-/TTCAACCGATT]TTCAACCGATTCTCA | 8450 |
rs749717302 | in-del | -/T | 0.00317376 | 0.039709 | intron-variant | CUL4B | GRCh38.p7 | X:120575023 | AAAGTACTATCTCAC[-/T]TATGATCTGAATCAG | 8450 |
rs749725544 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120531127 | AGGAGTTCAAGACCT[C/G]CCTGGTCAATATGGT | 8450 |
rs749726413 | snp | C/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120570248 | GAATAGGGTTTGACA[C/T]GTGCAAAGTAAGACA | 8450 |
rs749827061 | snp | A/G | 2.33803e-05 | 0.00341901 | intron-variant | CUL4B | GRCh38.p7 | X:120538773 | AAAACATCCTTGCCT[A/G]TGTAAAAAGAAATGC | 8450 |
rs749835337 | in-del | -/TACCACATT | 2.30979e-05 | 0.0033983 | intron-variant | CUL4B | GRCh38.p7 | X:120535987 | AAGCTCTGTATCCAA[-/TACCACATT]TACCATTTTTATACT | 8450 |
rs749885489 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120549878 | TCAGCATTTCTTATC[A/G]CTTTGCTTAGATTCT | 8450 |
rs749923093 | snp | A/G | 9.17642e-05 | 0.00677301 | synonymous-codon, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120560312 | CGCATCAAACCCTAC[A/G]AACTCCAGGGTGTCT | 8450 |
rs749948361 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | CUL4B | GRCh38.p7 | X:120573739 | ATCCCAGTTTTCTCT[A/G]GGAAAATTTGTTTCT | 8450 |
rs749971401 | snp | C/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120549474 | CATCAACCCGGGCGG[C/T]GGAGGTTGCAGTGAG | 8450 |
rs749994745 | snp | C/T | 0.00158814 | 0.0281345 | utr-variant-3-prime | CUL4B | GRCh38.p7 | X:120526334 | TTTGATAAATACATC[C/T]AGAACTCTGTACAGT | 8450 |
rs750012942 | snp | C/T | 2.27951e-05 | 0.00337595 | intron-variant, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120560076 | TATGGATTTTGGCCT[C/T]GGTTACCTTTAAAGT | 8450 |
rs750046695 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | CUL4B | GRCh38.p7 | X:120549000 | AGTTTCCTGTTATGC[A/G]TATATAAAAGACTTT | 8450 |
rs750060927 | snp | A/C | 0.00105904 | 0.0229869 | upstream-variant-2KB, intron-variant | CUL4B | GRCh38.p7 | X:120561071 | GTTATTGTCAATAGC[A/C]CAAGAGGCTAAAGAT | 8450 |
rs750062247 | snp | A/G | | | intron-variant | CUL4B | GRCh38.p7 | X:120551347 | GGATTACAAGCATGC[A/G]CCGCCACACTCAGCT | 8450 |
rs750062298 | snp | A/G | | | intron-variant | CUL4B | GRCh38.p7 | X:120527410 | TTTTGATTTTTTTTT[A/G]GAGCTTTTAATTTTT | 8450 |
rs750076219 | snp | A/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120528990 | TAAAATGACCACTTG[A/T]TCAAGAGGGGAAAAG | 8450 |
rs750109050 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120534696 | ATTTAGAAACATGAT[C/T]AGCATTATCCAGCAA | 8450 |
rs750123719 | snp | A/G | 3.56379e-05 | 0.0042211 | synonymous-codon | CUL4B | GRCh38.p7 | X:120539359 | TGCACGAAGTTTTGA[A/G]TCTACATACTTAGCT | 8450 |
rs750144966 | snp | A/G | 6.92985e-05 | 0.00588595 | missense | CUL4B | GRCh38.p7 | X:120544615 | GATCACTTATAATAT[A/G]AGCCCTAAATAACTC | 8450 |
rs750182963 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120556509 | GACAGGTAGGGCAAA[C/T]TATTATTTCCTCTAC | 8450 |
rs750186931 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120566586 | GTTTTTAGTAGAGAC[A/G]GGGTTTCTCCATGTT | 8450 |
rs750276715 | in-del | -/TA | 0.00581083 | 0.0535878 | intron-variant | CUL4B | GRCh38.p7 | X:120566328 | AACAGATTTCATATG[-/TA]TGTGTGTGTGTATAG | 8450 |
rs750308553 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120530942 | TTAAAAGTAAGGACA[C/T]GGTAATCCTTTAAGA | 8450 |
rs750312282 | snp | A/C | | | upstream-variant-2KB, intron-variant | CUL4B | GRCh38.p7 | X:120563479 | TGGCCTCAAGTGATC[A/C]GCCTGCCTCAGCCTC | 8450 |
rs750377789 | snp | A/G | 2.2791e-05 | 0.00337564 | synonymous-codon | CUL4B | GRCh38.p7 | X:120574567 | ACCGTCTTTAGAGGT[A/G]GTAGCCTCATCATCA | 8450 |
rs750387622 | snp | C/T | 2.88189e-05 | 0.00379587 | intron-variant | CUL4B | GRCh38.p7 | X:120546497 | TTGAAGAAATGTTTT[C/T]AACTATTAATACAAT | 8450 |
rs750405937 | snp | A/G | | | intron-variant | CUL4B | GRCh38.p7 | X:120541424 | GAATCACTTGAACCT[A/G]GGAGGCAGAGGTTGC | 8450 |
rs750407098 | in-del | -/AA | | | intron-variant | CUL4B | GRCh38.p7 | X:120534949 | TAGTCATGAAAAGCT[-/AA]AGTTTTTTGAGATTA | 8450 |
rs750415949 | snp | C/G | | | intron-variant | CUL4B | GRCh38.p7 | X:120564908 | GAGTTCAACTCATAC[C/G]TTAGAAACATTAATT | 8450 |
rs750429458 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120540215 | AGTACTTACATCCAG[A/G]TTTTTAGAAACACTC | 8450 |
rs750431108 | snp | C/T | 3.46669e-05 | 0.0041632 | upstream-variant-2KB, intron-variant | CUL4B | GRCh38.p7 | X:120561365 | CTTCGCGCCGCAGCG[C/T]CCTTACCGGAAGTGA | 8450 |
rs750433295 | in-del | -/TAAT | 0.00211696 | 0.0324653 | intron-variant | CUL4B | GRCh38.p7 | X:120528468 | AGTGGCTCATGCCTG[-/TAAT]TAATCCCAGCACTTT | 8450 |
rs750435583 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | CUL4B | GRCh38.p7 | X:120564376 | TTTGGGAGGCTGAGG[C/T]GGGCCGATCACCTGA | 8450 |
rs750518304 | snp | C/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120543251 | ATTTTAAAAAAACAC[C/T]GCATATTTTAGAATT | 8450 |
rs750522987 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120572315 | CTTAAAAAATATAAA[A/T]TTAGCCGGGTGTGGT | 8450 |
rs750535134 | snp | C/T | 0.00105904 | 0.0229869 | upstream-variant-2KB, intron-variant | CUL4B | GRCh38.p7 | X:120563395 | ATGTATCACTACGCC[C/T]GCTAATTTTTTTTGT | 8450 |
rs750626614 | snp | A/G | 2.51073e-05 | 0.00354303 | synonymous-codon | CUL4B | GRCh38.p7 | X:120542988 | AAGAATTGCTGTTAA[A/G]TGTTCACCTAGAAGT | 8450 |
rs750652680 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | CUL4B | GRCh38.p7 | X:120537969 | GGTCAAATATACTTA[C/T]ATTTCACCAATTTTT | 8450 |
rs750672501 | snp | G/T | 4.1266e-05 | 0.00454217 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | CUL4B | GRCh38.p7 | X:120561444 | GCAGGACTTGAGTGG[G/T]GGGGGGAAGGGGGGA | 8450 |
rs750693828 | snp | C/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120555224 | ATGTATCAGGAAAAG[C/T]ATTTTCAAATCAAAA | 8450 |
rs750694336 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120571394 | AGCTGGCAGAGATAA[C/G]AAATGACAACTAGGA | 8450 |
rs750725474 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120537270 | TGACCTCATTACAGG[C/T]GTTATCAACTTAAAT | 8450 |
rs750771460 | snp | C/T | 0.00370173 | 0.0428621 | intron-variant | CUL4B | GRCh38.p7 | X:120533979 | GCAGAGGCAGGAGAA[C/T]TGCTTGAACACAGGA | 8450 |
rs750824070 | in-del | -/T | 0.000250701 | 0.0111932 | intron-variant | CUL4B | GRCh38.p7 | X:120534433 | TGTCCCCCAGACCTC[-/T]TAACATAGTGGTGTG | 8450 |
rs750866615 | snp | G/T | 2.29085e-05 | 0.00338433 | missense | CUL4B | GRCh38.p7 | X:120543782 | CTTCTTCTAGACGTT[G/T]GTTAACATGATGTAG | 8450 |
rs750950939 | snp | A/G | | | intron-variant | CUL4B | GRCh38.p7 | X:120533895 | ACATGGTGAAACCCC[A/G]TCTCTACTAAAAATA | 8450 |
rs750954285 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120529621 | TCAGTTTACCAGAAC[C/T]ATCACTACACTTTTC | 8450 |
rs750971013 | snp | C/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120536244 | ACTGTTGCTTCTGCA[C/T]TGGTTTCCTTCACAG | 8450 |
rs750996894 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120553770 | AAAACAAAACACTGC[A/G]GCTACTCATACAAAA | 8450 |
rs751011702 | snp | C/T | 0.000529661 | 0.016265 | upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120577167 | TAGATTTATACAGCT[C/T]ATTTTGTTTTCTTGT | 8450 |
rs751036464 | snp | C/T | 0.00211696 | 0.0324653 | intron-variant | CUL4B | GRCh38.p7 | X:120541491 | GTGACGAGAGCAAAA[C/T]TCTGTCTCAAAAAAA | 8450 |
rs751062532 | snp | C/T | 0.0026455 | 0.0362733 | upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120575959 | GTGGGGGATGGGAGA[C/T]GGGAACTGGAGCCTT | 8450 |
rs751075437 | snp | A/G | 0.0199387 | 0.0978356 | intron-variant | CUL4B | GRCh38.p7 | X:120566365 | TATATATATATATAT[A/G]TATATATATATATAT | 8450 |
rs751113869 | snp | C/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120570053 | AAGGCAGCATCCCAA[C/T]CTCAAGTCTGGTACA | 8450 |
rs751150824 | snp | C/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120571907 | GAGTTGAATATGCAC[C/T]GATTTTGGTATCTGC | 8450 |
rs751182436 | snp | C/G | 4.56069e-05 | 0.00477508 | intron-variant, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120560056 | TCAAATCCTTATTAG[C/G]TGATTATGGATTTTG | 8450 |
rs751198914 | snp | A/G | | | intron-variant | CUL4B | GRCh38.p7 | X:120549327 | GGGAGGCCGAGGCGG[A/G]CAGATCATGAGGTCT | 8450 |
rs751214291 | snp | C/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120547523 | TTTTGAGTGCCAACA[C/T]GCTGCTCAAAGAAAA | 8450 |
rs751231161 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120550024 | CGGCACATCTACTTA[C/T]CTTCTCACACAAGAT | 8450 |
rs751259899 | snp | C/T | 2.28053e-05 | 0.0033767 | intron-variant | CUL4B | GRCh38.p7 | X:120574510 | GCCTGTTAACAATTA[C/T]TTAGACTTAACTCTT | 8450 |
rs751341660 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120557216 | GTGCCCGGCCTGAAG[C/T]ATCTTTTAACACCAA | 8450 |
rs751344215 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120547051 | CAAAATACAGGCATT[C/T]TACTTCAAGCTGGGT | 8450 |
rs751358214 | snp | C/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120526925 | CATTTAGTTAATACC[C/T]CATTAAAAAGACAAC | 8450 |
rs751376524 | snp | A/T | 2.2946e-05 | 0.00338711 | intron-variant | CUL4B | GRCh38.p7 | X:120538623 | ACATTCTCCTTCAGG[A/T]ATCAAAGAAAAGGAA | 8450 |
rs751458452 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | CUL4B | GRCh38.p7 | X:120542636 | ATTTAAAGAGACGAG[A/G]GTCTCACTATGTTGC | 8450 |
rs751464618 | snp | A/G | | | downstream-variant-500B | CUL4B | GRCh38.p7 | X:120524193 | TTTGAGGAACATCTT[A/G]CTCTGAGAGTATCTG | 8450 |
rs751498976 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120566686 | ACAGGTGTGAGCCAC[C/T]GCACCCAGCCAAATT | 8450 |
rs751504082 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120531595 | CTCCCAAGTAGCTGG[G/T]ACTACAAGCACGCAC | 8450 |
rs751516894 | snp | A/C | 2.28011e-05 | 0.00337639 | splice-acceptor-variant | CUL4B | GRCh38.p7 | X:120574631 | ATCCGTCCTTTGGGT[A/C]TACGATAGAAAACAG | 8450 |
rs751549630 | snp | A/G | | | upstream-variant-2KB, intron-variant | CUL4B | GRCh38.p7 | X:120562054 | GTATTCTAAGGCGAA[A/G]AAATGGAAAGGTAAC | 8450 |
rs751584306 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120555139 | GCAGGTAAAACTTAC[A/G]AAGTACAAGAAAACA | 8450 |
rs751620032 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | CUL4B | GRCh38.p7 | X:120565216 | GTCCTCTCCAGATAT[C/T]TCATACCAGTGGCTT | 8450 |
rs751642753 | snp | C/G | | | upstream-variant-2KB, intron-variant | CUL4B | GRCh38.p7 | X:120563309 | TGTAATCTTGGCTCA[C/G]TGCAACCTCTGCCTC | 8450 |
rs751669743 | snp | C/T | 2.27951e-05 | 0.00337595 | synonymous-codon | CUL4B | GRCh38.p7 | X:120535860 | TTTTAACACACAGTG[C/T]CCTAGGGTTGACTGC | 8450 |
rs751729066 | in-del | -/TG | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120530584 | GATATATCTTCTAAA[-/TG]TGTGTATCAGTTTCA | 8450 |
rs751734223 | in-del | -/C | 9.13576e-05 | 0.00675799 | utr-variant-3-prime | CUL4B | GRCh38.p7 | X:120526737 | CTACTGCATATGACA[-/C]CCAAATGCTGCAAGG | 8450 |
rs751753785 | snp | A/G | 2.3084e-05 | 0.00339728 | intron-variant | CUL4B | GRCh38.p7 | X:120532645 | AGCATGAACAACTAC[A/G]ACATTCTACCTCAAT | 8450 |
rs751775348 | snp | A/C | 0.00105904 | 0.0229869 | intron-variant | CUL4B | GRCh38.p7 | X:120573282 | TCCATGACAGTATAT[A/C]GAGATCTACCTCATT | 8450 |
rs751778492 | snp | C/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120541117 | ATCAATCAGGTTTTA[C/T]AGCTGATATGCCACA | 8450 |
rs751816892 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120529787 | CCATGGTATTTCAAG[A/T]GGAAAAGAAGTAAAT | 8450 |
rs751833365 | snp | A/G | 0.000822537 | 0.0202631 | synonymous-codon | CUL4B | GRCh38.p7 | X:120538715 | AGATGCACTCTTTCC[A/G]ACTAACAGGCGCTTG | 8450 |
rs751855056 | snp | C/G | | | intron-variant | CUL4B | GRCh38.p7 | X:120574682 | TCCTCTCCCATATCT[C/G]TATAGTGTTATGAAT | 8450 |
rs751888920 | snp | G/T | 2.64743e-05 | 0.00363819 | intron-variant | CUL4B | GRCh38.p7 | X:120542957 | TCTTATTTACAAATT[G/T]CCAATTACCTTTCTG | 8450 |
rs751902328 | snp | A/T | 0.00105904 | 0.0229869 | intron-variant | CUL4B | GRCh38.p7 | X:120570207 | GCTCACTCTTAGATA[A/T]AGGAGGTGAGAATCA | 8450 |
rs751904516 | snp | A/T | 0.000529661 | 0.016265 | upstream-variant-2KB, intron-variant | CUL4B | GRCh38.p7 | X:120561284 | CGCGATCCCCTTTCC[A/T]GGCAGCGCCTTCCTT | 8450 |
rs751912130 | snp | G/T | 0.000529661 | 0.016265 | utr-variant-3-prime | CUL4B | GRCh38.p7 | X:120525688 | AGGGTTTTAGCAAGT[G/T]AAAATGAAGATGACA | 8450 |
rs751977121 | snp | A/G | 2.28097e-05 | 0.00337703 | intron-variant | CUL4B | GRCh38.p7 | X:120541554 | ATATGCACTCTTGAT[A/G]TGTAGATAAGCCATA | 8450 |
rs751977170 | snp | A/G | 0.000168965 | 0.00918987 | upstream-variant-2KB, intron-variant | CUL4B | GRCh38.p7 | X:120561348 | AACGGTCCCGCGGGA[A/G]GCTTCGCGCCGCAGC | 8450 |
rs752013506 | snp | A/C | | | intron-variant | CUL4B | GRCh38.p7 | X:120531942 | TGACATTATGTACTA[A/C]GACTCCTAAAATGTT | 8450 |
rs752042728 | snp | C/G | 0.00528398 | 0.051128 | intron-variant | CUL4B | GRCh38.p7 | X:120546243 | GAGGAAGAGTGGGAG[C/G]GGGGCGAGGGATAAA | 8450 |
rs752085197 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | CUL4B | GRCh38.p7 | X:120534857 | AATTAATCAGCCTTA[C/T]GTGTCATTCTAGATA | 8450 |
rs752102639 | snp | C/G | | | intron-variant | CUL4B | GRCh38.p7 | X:120554566 | AGTGTACTTAGAACA[C/G]CATGTTCTTTTATAG | 8450 |
rs752119011 | snp | C/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120556668 | AACATAGCAAGACCC[C/T]TATCTCTTAAAAAAA | 8450 |
rs752130919 | snp | C/T | 8.11293e-05 | 0.00636852 | missense | CUL4B | GRCh38.p7 | X:120545508 | ACAAAAAAATGCTCC[C/T]GATCATGATCTGCCA | 8450 |
rs752181556 | in-del | -/AAG | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120557506 | GCAAAGTCTACTATT[-/AAG]AAGGAGGTAGAATAA | 8450 |
rs752188871 | in-del | -/GCTTCTTCTGTATC | 4.61659e-05 | 0.00480425 | frameshift-variant, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120560338 | TGTCTTCAAAACGCA[-/GCTTCTTCTGTATC]GGTACGTGGCTGGAA | 8450 |
rs752209980 | snp | A/G | 2.70223e-05 | 0.00367565 | intron-variant | CUL4B | GRCh38.p7 | X:120532403 | GTGTGTTAGGACTAA[A/G]AGAAAGTGAAAGAAA | 8450 |
rs752222658 | snp | A/T | 0.00370173 | 0.0428621 | intron-variant | CUL4B | GRCh38.p7 | X:120566794 | TTCCTTAGCTCAGAG[A/T]TTTTATCTGTCATAC | 8450 |
rs752224830 | snp | C/T | 0.000529661 | 0.016265 | upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120576885 | TAGTCCATCCTGGGT[C/T]AGGTGCCCAGCCACA | 8450 |
rs752338782 | snp | A/G | | | intron-variant | CUL4B | GRCh38.p7 | X:120566269 | AAAGCAAGGAAAGTA[A/G]TAACATGTGCTGAAC | 8450 |
rs752362511 | snp | A/C | 0.00105904 | 0.0229869 | intron-variant | CUL4B | GRCh38.p7 | X:120541925 | AAATATAGAGACTTT[A/C]GTCGCTATAAAAATA | 8450 |
rs752363861 | snp | A/C/G/T | 0.000375718 | 0.0137015 | missense | CUL4B | GRCh38.p7 | X:120547149 | ATTCTCTGAATTGAT[A/C/G/T]AATCTGTGCTTTGAT | 8450 |
rs752369582 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120542774 | GGATCCCTCTCTTCT[A/T]GTTCCTGTATCTTTC | 8450 |
rs752386358 | snp | C/T | 0.000529661 | 0.016265 | upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120576075 | TTGGCTTGACTAGAT[C/T]AGCTATCTAAAATTT | 8450 |
rs752429684 | snp | C/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120545019 | ATCAACTGGTTTCAA[C/T]ACTGAAGAATCAGTG | 8450 |
rs752455768 | snp | C/T | 2.37767e-05 | 0.00344787 | intron-variant | CUL4B | GRCh38.p7 | X:120537079 | TCTTAAAACTGCATA[C/T]ATTTCATATCATAAT | 8450 |
rs752494924 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120537993 | AATTTTTTTTTCTAC[C/T]GTGAATATCACCTCA | 8450 |
rs752543393 | snp | C/G | 2.7105e-05 | 0.00368128 | missense, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120557948 | TTCTTCTAAATTGTA[C/G]TTAATTGAAGTACTA | 8450 |
rs752550547 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120548230 | AGTGAACCATGACTA[C/T]GCCACTGCACTCTAG | 8450 |
rs752557937 | snp | G/T | 4.61643e-05 | 0.00480417 | intron-variant | CUL4B | GRCh38.p7 | X:120535979 | CTTTATTTAAGCTCT[G/T]TATCCAATACCACAT | 8450 |
rs752630655 | snp | A/G | 0.000529661 | 0.016265 | intron-variant, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120558760 | GCAATGAGTGTGGGG[A/G]AAAAAGTTTTAATTA | 8450 |
rs752667077 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120546335 | CCACTAAGGAACTTA[C/T]TCATGTAACCAAATG | 8450 |
rs752710403 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120569474 | CACGCCATTCTCCTG[C/T]CTCAGCCTCCGGAGT | 8450 |
rs752732655 | snp | C/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120574493 | GTGAGCCACCGCGCC[C/T]GGCCTGTTAACAATT | 8450 |
rs752791681 | snp | G/T | 0.000112784 | 0.00750862 | intron-variant | CUL4B | GRCh38.p7 | X:120545553 | AATCAAACAAGTTTT[G/T]TATGTTGTGAAGCTG | 8450 |
rs752793334 | snp | C/T | 2.2805e-05 | 0.00337668 | missense | CUL4B | GRCh38.p7 | X:120530242 | TTTCTGTAGTGCTTG[C/T]TTGTTCTTCAACCTA | 8450 |
rs752853055 | snp | C/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120536607 | CCCAGAAATTTGGCA[C/T]TATTAGCTATGTGCT | 8450 |
rs752877528 | snp | C/T | 2.30258e-05 | 0.00339299 | synonymous-codon | CUL4B | GRCh38.p7 | X:120544592 | AATTGTCTTATTCTG[C/T]ACTTTCTGATCACTT | 8450 |
rs752944156 | in-del | -/A | | | intron-variant | CUL4B | GRCh38.p7 | X:120555942 | GCAAGACTCCATCTC[-/A]AAAAAAAAAAAAAAA | 8450 |
rs752972392 | snp | A/C | | | intron-variant | CUL4B | GRCh38.p7 | X:120538027 | GCCATGAATTACAAC[A/C]AACACGTTTCTATTT | 8450 |
rs752972512 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120530713 | ACTAGTTAAGAGTCA[A/G]CCTCTTTGAAAATTA | 8450 |