SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs15677 | snp | A/G | 0.366266 | 0.221319 | utr-variant-3-prime | CUL5 | GRCh38.p7 | 11:108106762 | GGTCTCTTCTCTCCA[A/G]CGTACACTTAAAATT | 8065 |
rs1052608 | snp | A/C | | | utr-variant-3-prime, intron-variant | CUL5 | GRCh38.p7 | 11:108104497 | ATTACATAAATATTA[A/C]AATCTCTGCCTTACC | 8065 |
rs1052609 | snp | A/C | | | utr-variant-3-prime, intron-variant | CUL5 | GRCh38.p7 | 11:108104498 | TTACATAAATATTAA[A/C]ATCTCTGCCTTACCT | 8065 |
rs1052612 | snp | C/G | | | utr-variant-3-prime | CUL5 | GRCh38.p7 | 11:108106703 | aaaaaaatCTTACCA[C/G]CAGTTTGTAAAGGTC | 8065 |
rs2037312 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | CUL5 | GRCh38.p7 | 11:108099252 | tcaagcaatatgcct[C/G]cctcggcctcccaaa | 8065 |
rs2056268 | snp | C/T | 0.0614824 | 0.164198 | intron-variant | CUL5 | GRCh38.p7 | 11:108091040 | ttagaattaaatttt[C/T]tttctttctttcttt | 8065 |
rs2271852 | snp | A/G | 0.454182 | 0.144256 | intron-variant | CUL5 | GRCh38.p7 | 11:108054576 | GACTCCTCAATATTT[A/G]TTTCATTTATTATAC | 8065 |
rs2271853 | snp | C/T | 0.309 | 0.242938 | intron-variant | CUL5 | GRCh38.p7 | 11:108054830 | TGATAATTTGAGCAA[C/T]TCCCTTGATATTCTT | 8065 |
rs2290294 | snp | A/G | 0.122064 | 0.214785 | intron-variant, upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108033653 | CTACAGGCTTAATCC[A/G]TTATTGAGGAATCAC | 8065 |
rs3736509 | snp | C/T | 0.34659 | 0.230587 | intron-variant | CUL5 | GRCh38.p7 | 11:108098057 | TGTGTTGTTTTGTTT[C/T]GTTTTTGTTTTTGTT | 8065 |
rs3781870 | snp | A/G | 0.167484 | 0.23599 | utr-variant-3-prime, intron-variant | CUL5 | GRCh38.p7 | 11:108105723 | ATAAAAATCCACGTT[A/G]AGCCATTCTTTCCTC | 8065 |
rs3781871 | snp | C/G | 0.246485 | 0.249975 | intron-variant | CUL5 | GRCh38.p7 | 11:108029981 | AAAAAAGAATACCTT[C/G]TTAACAAGAGGATAC | 8065 |
rs3847562 | snp | C/T | 0.0166427 | 0.0896904 | intron-variant | CUL5 | GRCh38.p7 | 11:108054600 | ATTATACTCAAAATA[C/T]TGATTTTGATCATAA | 8065 |
rs3847563 | snp | A/G | 0.0569829 | 0.158885 | intron-variant | CUL5 | GRCh38.p7 | 11:108066584 | TCACCTTGTAATAAA[A/G]TTGTAATAAAGTAGC | 8065 |
rs3858391 | snp | C/T | 0.0832709 | 0.186283 | intron-variant | CUL5 | GRCh38.p7 | 11:108020075 | tacatgagggatcca[C/T]caccatgacccaaca | 8065 |
rs3858392 | snp | C/T | 0.348574 | 0.229746 | intron-variant | CUL5 | GRCh38.p7 | 11:108021730 | ccacgagtttgaaac[C/T]agcctgggcaacatg | 8065 |
rs3858393 | snp | A/T | 0.0618563 | 0.164627 | intron-variant | CUL5 | GRCh38.p7 | 11:108027751 | ccactctaatctggt[A/T]tttgtccttactact | 8065 |
rs3858394 | snp | C/T | 0.355525 | 0.226637 | intron-variant | CUL5 | GRCh38.p7 | 11:108041323 | GCCACTGCACTCCAG[C/T]CTGGGCAACAGAGAC | 8065 |
rs3858395 | snp | A/G | 0.455621 | 0.142197 | intron-variant | CUL5 | GRCh38.p7 | 11:108059036 | AGGCAGAGTCTCGCT[A/G]TGTTGCCCAGGCTGG | 8065 |
rs3858396 | snp | A/C | 0.478768 | 0.100824 | intron-variant | CUL5 | GRCh38.p7 | 11:108061665 | ATATAGGAATGCAGG[A/C]GGGAAGGGAGGCAAA | 8065 |
rs3858397 | snp | A/G | 0.0919752 | 0.193722 | intron-variant | CUL5 | GRCh38.p7 | 11:108078734 | CAATAAAGGTTAGTT[A/G]AAAAAAGTCTTTTGA | 8065 |
rs3908130 | snp | C/T | 0.0573587 | 0.15934 | intron-variant | CUL5 | GRCh38.p7 | 11:108017040 | ATGAACAAACCACAG[C/T]TACACAGATCAATTA | 8065 |
rs3908131 | snp | A/G | 0.332337 | 0.236052 | intron-variant | CUL5 | GRCh38.p7 | 11:108016928 | tatgctgcccaatct[A/G]gtctccaactcctgg | 8065 |
rs3911815 | snp | A/G | 0.453939 | 0.144598 | intron-variant | CUL5 | GRCh38.p7 | 11:108061999 | ggaggtgattggatc[A/G]gcaaggtttccccca | 8065 |
rs3950984 | snp | C/T | 0.459118 | 0.137002 | intron-variant | CUL5 | GRCh38.p7 | 11:108012876 | TGTTGGGATTACAGG[C/T]GTGAGCCACTGCACT | 8065 |
rs4027717 | in-del | -/T/TT | 0 | 0 | intron-variant | CUL5 | GRCh38.p7 | 11:108099022 | ttttttttttttttt[-/T/TT]ngagacagggtctca | 8065 |
rs4028252 | snp | C/T | 0.0573587 | 0.15934 | intron-variant | CUL5 | GRCh38.p7 | 11:108013519 | TGTGTGCGTACACAC[C/T]CCTACTTAGCTGGTT | 8065 |
rs4109081 | snp | A/G | 0.477175 | 0.104362 | intron-variant | CUL5 | GRCh38.p7 | 11:108097147 | CTGAGCCCCCCAAGT[A/G]GCTGGGACTACAGGT | 8065 |
rs4430476 | snp | C/T | 0.465473 | 0.126772 | intron-variant | CUL5 | GRCh38.p7 | 11:108091874 | CTCAACATGTTGGCT[C/T]CTGCTTATCCCAAAT | 8065 |
rs4453201 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | CUL5 | GRCh38.p7 | 11:108053031 | ATTTCTTGGCAAGTC[G/T]TTTTAGTGAACTAAA | 8065 |
rs4503496 | snp | C/T | 0.463989 | 0.129263 | intron-variant | CUL5 | GRCh38.p7 | 11:108062360 | TAAATACCAAACTGA[C/T]TTTCAGGAATGTAGT | 8065 |
rs4508171 | snp | C/G | 0.456095 | 0.141508 | intron-variant | CUL5 | GRCh38.p7 | 11:108063860 | cccaccatcattata[C/G]gagggttcctttttc | 8065 |
rs4565865 | snp | C/G | 0.198324 | 0.244601 | intron-variant | CUL5 | GRCh38.p7 | 11:108035540 | ccaggagttcaagac[C/G]agcctgggcaacata | 8065 |
rs4568970 | snp | C/G | 0.448963 | 0.151372 | intron-variant | CUL5 | GRCh38.p7 | 11:108025929 | TTTGGACATTTGTAG[C/G]GCTCACCTCATTTGT | 8065 |
rs4568971 | snp | C/T | 0.449218 | 0.151037 | intron-variant | CUL5 | GRCh38.p7 | 11:108026159 | ctttttgcttccttg[C/T]ccctgtcttgttctg | 8065 |
rs4575229 | snp | A/G | 0.455621 | 0.142197 | intron-variant | CUL5 | GRCh38.p7 | 11:108069315 | CTTCCTTCCCTACCT[A/G]TGAAATAAAACCCCA | 8065 |
rs4753827 | snp | G/T | 0.365024 | 0.221967 | intron-variant | CUL5 | GRCh38.p7 | 11:108016603 | TGAACCCAGTTGTCA[G/T]TAAGAGCCATTTGCC | 8065 |
rs4754286 | snp | A/G | 0.44638 | 0.154709 | intron-variant | CUL5 | GRCh38.p7 | 11:108019967 | gtggggagaggtacc[A/G]ggctctttttaacaa | 8065 |
rs4754287 | snp | A/G | 0.482083 | 0.0929373 | intron-variant | CUL5 | GRCh38.p7 | 11:108020327 | cccattcaggttagc[A/G]ttcccgaagactttc | 8065 |
rs4754288 | snp | C/T | 0.0807149 | 0.183963 | intron-variant | CUL5 | GRCh38.p7 | 11:108043156 | TAGCTCATTGTAACC[C/T]TGAACTTCTGAGTTC | 8065 |
rs4754289 | snp | G/T | 0.0566069 | 0.158427 | intron-variant | CUL5 | GRCh38.p7 | 11:108053849 | ACACCTGGCTAATTT[G/T]TTTCTTTTTTTTTCT | 8065 |
rs4754291 | snp | A/G | 0.0581099 | 0.160244 | intron-variant | CUL5 | GRCh38.p7 | 11:108075675 | TGAGTTTCTGGGACT[A/G]TGAGCACATACCACC | 8065 |
rs4754292 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | CUL5 | GRCh38.p7 | 11:108075720 | TTTTAAAGTTTTTCT[A/G]TAGAGACAACATCTA | 8065 |
rs6144502 | snp | A/C | | | intron-variant | CUL5 | GRCh38.p7 | 11:108022094 | aagtgatcctcccac[A/C]gtgctggaattatag | 8065 |
rs6588997 | snp | C/G | 0.093417 | 0.194889 | intron-variant | CUL5 | GRCh38.p7 | 11:108029925 | TAATTTTATAAATTA[C/G]CAAAAGTGCTTGTGG | 8065 |
rs6588998 | snp | A/G | 0.198324 | 0.244601 | intron-variant | CUL5 | GRCh38.p7 | 11:108034683 | tgaaaagcaaaaatc[A/G]ttaatgtcctcctcc | 8065 |
rs7101529 | snp | C/T | 0.0360663 | 0.129354 | intron-variant | CUL5 | GRCh38.p7 | 11:108082660 | tttctgtttcttttt[C/T]ttcagacagggtttc | 8065 |
rs7103534 | snp | C/T | 0.195837 | 0.244062 | intron-variant | CUL5 | GRCh38.p7 | 11:108040925 | ATTTCTAGGGAATTA[C/T]CTAACTCCACCCCCT | 8065 |
rs7104710 | snp | A/T | 0.0150606 | 0.0854603 | intron-variant | CUL5 | GRCh38.p7 | 11:108067903 | TCTTAACCATTTTAT[A/T]TGTGTAGTCTTTTCt | 8065 |
rs7104942 | snp | A/G | 0.361894 | 0.223562 | intron-variant | CUL5 | GRCh38.p7 | 11:108067851 | TAAGATTACTCAGCA[A/G]TTGGGGCAGAGATTT | 8065 |
rs7105163 | snp | G/T | 0.364401 | 0.222289 | intron-variant | CUL5 | GRCh38.p7 | 11:108075244 | AATGCAGGGACGATA[G/T]CGTGGCGTATTAGTA | 8065 |
rs7105261 | snp | C/G | 0.0509478 | 0.151255 | intron-variant | CUL5 | GRCh38.p7 | 11:108103104 | cccggcATATACATG[C/G]CTTTTGTTGGGTAAA | 8065 |
rs7106586 | snp | C/T | 0.0368353 | 0.130617 | intron-variant | CUL5 | GRCh38.p7 | 11:108077036 | ctggaaaaatatgtt[C/T]ggcagcttcagcata | 8065 |
rs7106930 | snp | C/T | 0.256061 | 0.249927 | intron-variant | CUL5 | GRCh38.p7 | 11:108091293 | tggtcttaagtgatc[C/T]gcctgcctcggcctc | 8065 |
rs7106986 | snp | C/G | 0.0558544 | 0.157504 | intron-variant | CUL5 | GRCh38.p7 | 11:108091101 | gtgttacccaggctg[C/G]attgcagtggtgcaa | 8065 |
rs7107097 | snp | A/T | 0.200182 | 0.244986 | intron-variant | CUL5 | GRCh38.p7 | 11:108077460 | catgatgaaaccctg[A/T]ctctattaaaaatac | 8065 |
rs7109537 | snp | G/T | 0.0839998 | 0.186933 | intron-variant | CUL5 | GRCh38.p7 | 11:108069037 | TGACAGGGGGATCAT[G/T]TGAGACCAGGAGTTT | 8065 |
rs7111660 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | CUL5 | GRCh38.p7 | 11:108092320 | cttaaaatgttgaac[A/G]tagagctgacccagc | 8065 |
rs7112974 | snp | A/G | 0.0154538 | 0.0865337 | utr-variant-3-prime, intron-variant | CUL5 | GRCh38.p7 | 11:108104538 | AACTATATTTTGCCA[A/G]TCACATTAGTTAGCA | 8065 |
rs7114631 | snp | C/G | 0.0368353 | 0.130617 | intron-variant | CUL5 | GRCh38.p7 | 11:108034541 | tcaggggtgctGGta[C/G]ttggtgctgttaggt | 8065 |
rs7117027 | snp | C/T | 0.0584853 | 0.160693 | intron-variant | CUL5 | GRCh38.p7 | 11:108102082 | gctggggtgcaatgg[C/T]gtgatcttggctcac | 8065 |
rs7117111 | snp | A/G | 0.442709 | 0.159259 | synonymous-codon, utr-variant-5-prime | CUL5 | GRCh38.p7 | 11:108046360 | TGAGTTTATTAAGCA[A/G]GCACAGGCAGTAAGT | 8065 |
rs7118335 | snp | C/T | 0.198014 | 0.244535 | intron-variant | CUL5 | GRCh38.p7 | 11:108041228 | TCCTTCACAGGTGTT[C/T]CCTTAGTAAATCTCT | 8065 |
rs7118566 | snp | C/G | 0.0573587 | 0.15934 | intron-variant | CUL5 | GRCh38.p7 | 11:108011175 | AGGTCTTTTTCTCCC[C/G]AAAAATAACTCTCAG | 8065 |
rs7120705 | snp | G/T | 0.377187 | 0.215229 | intron-variant | CUL5 | GRCh38.p7 | 11:108067790 | TCTGGTTTCACTGCT[G/T]AAGGTGGAAGTGTTT | 8065 |
rs7120711 | snp | A/G | 0.375996 | 0.215928 | intron-variant | CUL5 | GRCh38.p7 | 11:108076730 | ttgggtatatgccta[A/G]aagagggattgctgg | 8065 |
rs7121079 | snp | C/T | 0.0618563 | 0.164627 | intron-variant | CUL5 | GRCh38.p7 | 11:108024201 | CTGCCCTGCCACTTA[C/T]TGCCTATAATTTTTG | 8065 |
rs7121568 | snp | A/T | 0.331874 | 0.236213 | intron-variant | CUL5 | GRCh38.p7 | 11:108015428 | TAACCAGAGAATTCT[A/T]TTTAATATGTCTAGT | 8065 |
rs7122356 | snp | C/G | 0.331874 | 0.236213 | intron-variant | CUL5 | GRCh38.p7 | 11:108011819 | TTTTAGTAGAGACAG[C/G]GTTTCACCATGTTGG | 8065 |
rs7124758 | snp | A/C | | | intron-variant | CUL5 | GRCh38.p7 | 11:108077631 | tgaaactctgtctcc[A/C]aaaaaaaaaaaagaa | 8065 |
rs7125285 | snp | A/G | 0.21915 | 0.248089 | intron-variant | CUL5 | GRCh38.p7 | 11:108055002 | GATTATTTGAAATAC[A/G]GAAGCATAGGAATGG | 8065 |
rs7125329 | snp | C/G | 0.0182019 | 0.0936463 | intron-variant | CUL5 | GRCh38.p7 | 11:108025110 | ttccaattatgtgta[C/G]gttaggtcatttgat | 8065 |
rs7125351 | snp | G/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108017747 | ctcagctacatggga[G/T]gctgaggcaggagga | 8065 |
rs7128487 | snp | A/G | 0 | 0 | intron-variant | CUL5 | GRCh38.p7 | 11:108061443 | ATAGAAATCTATACC[A/G]TAATTGTTCTCTTCA | 8065 |
rs7130999 | snp | C/T | 0.44638 | 0.154709 | intron-variant | CUL5 | GRCh38.p7 | 11:108035015 | ggggacagctgcatt[C/T]aataaccagactgac | 8065 |
rs7480645 | snp | A/C | | | intron-variant | CUL5 | GRCh38.p7 | 11:108022093 | caagtgatcctccca[A/C]cgtgctggaattata | 8065 |
rs7925170 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | CUL5 | GRCh38.p7 | 11:108089947 | TGGGAGGCTGAGGCA[A/G]GAGAATCACTTGAAC | 8065 |
rs7927717 | snp | G/T | 0.198014 | 0.244535 | intron-variant | CUL5 | GRCh38.p7 | 11:108044919 | GGTGCACACCACCAC[G/T]CCTGGCTAATTTTTG | 8065 |
rs7930830 | snp | G/T | 0.456803 | 0.140473 | intron-variant | CUL5 | GRCh38.p7 | 11:108012097 | CTGAAAACCTTTCCA[G/T]GTAACTACTTTATCT | 8065 |
rs7931789 | snp | C/T | 0.0807149 | 0.183963 | intron-variant | CUL5 | GRCh38.p7 | 11:108059940 | GAATTAAATGAAATA[C/T]GTTACATTAAGCATT | 8065 |
rs7931791 | snp | A/T | 0.0569829 | 0.158885 | intron-variant | CUL5 | GRCh38.p7 | 11:108059942 | ATTAAATGAAATATG[A/T]TACATTAAGCATTTG | 8065 |
rs7934496 | snp | A/G | 0.078151 | 0.181571 | intron-variant | CUL5 | GRCh38.p7 | 11:108052252 | ttgggattaGACCAC[A/G]CGCAGTCGACCCTTC | 8065 |
rs7935031 | snp | C/T | 0.0584853 | 0.160693 | intron-variant | CUL5 | GRCh38.p7 | 11:108101203 | CTACTCCATTCATCC[C/T]CATTCATTGCTATTT | 8065 |
rs7935911 | snp | C/T | 0.448963 | 0.151372 | intron-variant | CUL5 | GRCh38.p7 | 11:108040164 | TTTTAAAAAGATTTA[C/T]CTTATAGCATGTTCC | 8065 |
rs7936826 | snp | A/G | 0.198944 | 0.244731 | intron-variant | CUL5 | GRCh38.p7 | 11:108027795 | tgtggacaaagtttc[A/G]gtaacttccatattg | 8065 |
rs7938410 | snp | A/T | 0.0970103 | 0.197722 | intron-variant | CUL5 | GRCh38.p7 | 11:108023094 | cctctactaaaaaaa[A/T]tagccgggcatggtg | 8065 |
rs7947012 | snp | A/C | 0.0150606 | 0.0854603 | intron-variant | CUL5 | GRCh38.p7 | 11:108048367 | ttgggctggtctcag[A/C]tgaatttgcctaagc | 8065 |
rs7947408 | snp | A/G | 0.198944 | 0.244731 | intron-variant | CUL5 | GRCh38.p7 | 11:108065593 | gtggtggtgagttca[A/G]tgcagtatctcacag | 8065 |
rs7947410 | snp | A/G | 0.449091 | 0.151204 | intron-variant | CUL5 | GRCh38.p7 | 11:108048397 | CTTATTAATGCAGCA[A/G]CAGTGGGCTGTTGGA | 8065 |
rs7948421 | snp | G/T | 0.269208 | 0.261944 | intron-variant | CUL5 | GRCh38.p7 | 11:108066157 | catcctggctaacac[G/T]gtgaaaccctgtttc | 8065 |
rs7949655 | snp | A/G | 0.256061 | 0.249927 | intron-variant | CUL5 | GRCh38.p7 | 11:108061495 | TGAAAGTTTTAAAAT[A/G]TTTACACAAGTAGAG | 8065 |
rs7951499 | snp | A/G | 0.0509478 | 0.151255 | intron-variant | CUL5 | GRCh38.p7 | 11:108043566 | TTTAATAGATTGGAG[A/G]GTTTCAAGAGTAGAT | 8065 |
rs9667757 | snp | C/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108009538 | GAACGCGGGTCTGTG[C/G]CCTTGGGGTCGACAG | 8065 |
rs9734272 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108077644 | CCAAAAAAAAAAAAA[A/G]AAAAAAAATCTCACT | 8065 |
rs9736047 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108077646 | aaaaaaaaaaaaaga[A/G]aaaaaaTCTCACTTG | 8065 |
rs9737019 | snp | A/C | | | intron-variant | CUL5 | GRCh38.p7 | 11:108039184 | caccaccacacctgg[A/C]taattttttgtattt | 8065 |
rs9888206 | snp | A/C | 0 | 0 | intron-variant | CUL5 | GRCh38.p7 | 11:108058548 | CCACTGCACCCGGCC[A/C]AAAGTGATTTTTTTT | 8065 |
rs10450616 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | CUL5 | GRCh38.p7 | 11:108028597 | taatcacagcacttt[C/G]ggaggccgaagcggg | 8065 |
rs10502101 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | CUL5 | GRCh38.p7 | 11:108060229 | TGTTCAAAAAGACAA[A/G]GTGATCCAGACTTTT | 8065 |
rs10691695 | in-del | -/TTTGT | | | intron-variant | CUL5 | GRCh38.p7 | 11:108068340 | TTTGTTTTGTTTTGT[-/TTTGT]GACAGTCTTGCTCTG | 8065 |
rs10736442 | snp | C/G | 0 | 0 | utr-variant-5-prime, upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108009161 | TGACCATGTAGGGGA[C/G]AAGAGTGAGGAAGCT | 8065 |
rs10736443 | snp | C/T | 0.0792508 | 0.182605 | intron-variant | CUL5 | GRCh38.p7 | 11:108071249 | AAATATTCCTTTGCA[C/T]TGAAAACCAAATGAC | 8065 |
rs10749913 | snp | A/C | 0 | 0 | intron-variant | CUL5 | GRCh38.p7 | 11:108070597 | GTCATCTCTGTCCCC[A/C]AAAATACTTTATAAG | 8065 |
rs10789650 | snp | G/T | 0.0599851 | 0.162463 | intron-variant | CUL5 | GRCh38.p7 | 11:108018566 | agtagtcccagctac[G/T]caggaggctgaggca | 8065 |
rs10789651 | snp | C/T | 0.449726 | 0.150364 | intron-variant | CUL5 | GRCh38.p7 | 11:108028255 | ATAAGCCTGTCAAAT[C/T]TTCTTTTATTCTAGT | 8065 |
rs10789652 | snp | C/T | 0.349013 | 0.229557 | intron-variant | CUL5 | GRCh38.p7 | 11:108042886 | CCTTGCCTTAGCCTC[C/T]TGAGTACCTGGGACT | 8065 |
rs10890795 | snp | C/T | 0.474091 | 0.11083 | intron-variant | CUL5 | GRCh38.p7 | 11:108010154 | AGACTTAGAACTAGT[C/T]TGTTCTGTGTATGTG | 8065 |
rs10890796 | snp | A/G | 0 | 0 | intron-variant | CUL5 | GRCh38.p7 | 11:108012571 | CTCCTATGCCTATAA[A/G]AAAGTTCATATGTCG | 8065 |
rs10890797 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | CUL5 | GRCh38.p7 | 11:108015814 | AAGTGGCAGCTCAGG[A/G]TAAATTTTGATCAGT | 8065 |
rs10890798 | snp | A/G | 0.469544 | 0.119585 | intron-variant | CUL5 | GRCh38.p7 | 11:108031291 | AATCACCTGACCCTG[A/G]GAGGTAGAGGCTATA | 8065 |
rs10890799 | snp | C/T | 0.0807149 | 0.183963 | intron-variant, upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108032204 | TTTTGTTGAAATTTA[C/T]TGGCCAAAACAAACC | 8065 |
rs10890800 | snp | C/T | 0.444229 | 0.157401 | intron-variant | CUL5 | GRCh38.p7 | 11:108033920 | TGTTTTCGTAAGTAC[C/T]CCACTAATTCTGTTT | 8065 |
rs10890802 | snp | A/T | 0.454544 | 0.143743 | intron-variant | CUL5 | GRCh38.p7 | 11:108056342 | TGAATGGGATTTAAA[A/T]TTTTTTTTTACTTTT | 8065 |
rs10890803 | snp | A/G | 0.452965 | 0.145963 | intron-variant | CUL5 | GRCh38.p7 | 11:108056426 | TTGTTCAGAAATCAC[A/G]CCGAGTTGGATGTCT | 8065 |
rs10890804 | snp | A/G | 0.463989 | 0.129263 | intron-variant | CUL5 | GRCh38.p7 | 11:108070476 | TGCTTTTAAAGGCCA[A/G]TTTAAACTGGAAACA | 8065 |
rs10890805 | snp | A/G | 0.465368 | 0.126951 | intron-variant | CUL5 | GRCh38.p7 | 11:108071324 | GGAATTCGATGGCAC[A/G]ATCACAATTCACTGT | 8065 |
rs10890806 | snp | G/T | 0.455977 | 0.141681 | intron-variant, downstream-variant-500B | CUL5 | GRCh38.p7 | 11:108074370 | CGGCTAATTTTTGTA[G/T]TTTTACTACAGACGG | 8065 |
rs10890807 | snp | A/T | 0.49543 | 0.0475834 | intron-variant | CUL5 | GRCh38.p7 | 11:108078131 | AAAAATTTATCTGTA[A/T]ATTTTCAATATTAAA | 8065 |
rs10890808 | snp | C/T | 0.45574 | 0.142025 | intron-variant | CUL5 | GRCh38.p7 | 11:108083284 | TCTGTCTGGTAGATA[C/T]ACTATAGCTTATTTA | 8065 |
rs10890809 | snp | C/T | 0.47614 | 0.106587 | intron-variant | CUL5 | GRCh38.p7 | 11:108086750 | tacccattcccagtt[C/T]gcaaagaaaggcata | 8065 |
rs10890810 | snp | A/G | 0.348574 | 0.229746 | intron-variant | CUL5 | GRCh38.p7 | 11:108103327 | GCACTTTGGGAGACC[A/G]GGGCAGGGGAGTATT | 8065 |
rs10890811 | snp | A/G | 0.433382 | 0.169915 | intron-variant | CUL5 | GRCh38.p7 | 11:108103415 | TAAAGAGAAGAAGGG[A/G]AAAAAAAAAACCTTA | 8065 |
rs11212484 | snp | A/C | 0.350982 | 0.228698 | intron-variant | CUL5 | GRCh38.p7 | 11:108013664 | AGTATATAACCGAAC[A/C]ACAAGATAAATCAAA | 8065 |
rs11212485 | snp | A/G | 0 | 0 | intron-variant | CUL5 | GRCh38.p7 | 11:108017107 | CCATTTTAAATTTCA[A/G]GCTGGGCACAGTGGC | 8065 |
rs11212486 | snp | A/G | 0.333261 | 0.235728 | intron-variant | CUL5 | GRCh38.p7 | 11:108017756 | ATGGGAGGCTGAGGC[A/G]GGAGGATTGCTTGAG | 8065 |
rs11212487 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | CUL5 | GRCh38.p7 | 11:108020141 | AATTTCAACATGAGG[C/G]TTGGTGGACAAACAT | 8065 |
rs11212488 | snp | A/G | 0.470521 | 0.117772 | intron-variant | CUL5 | GRCh38.p7 | 11:108023655 | TCATTTATGTGCCCC[A/G]ATGCACAGTAGAGTC | 8065 |
rs11212489 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | CUL5 | GRCh38.p7 | 11:108023932 | CAGTGTCCTCTTCCT[C/T]CTCCTCCACCATGTT | 8065 |
rs11212490 | snp | C/T | 0.472147 | 0.114677 | intron-variant, upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108032601 | TCTCTCTCTCTCTCT[C/T]TGTTTTTGGCAATGT | 8065 |
rs11212491 | snp | G/T | 0.448066 | 0.152544 | intron-variant | CUL5 | GRCh38.p7 | 11:108038535 | CAAAAATTACCTGAG[G/T]GCGGTGGTGGGCCTC | 8065 |
rs11212492 | snp | C/T | 0.0596104 | 0.162024 | intron-variant | CUL5 | GRCh38.p7 | 11:108040724 | AGGAGTTTTAAGTTA[C/T]GAGCTTATCATGCCA | 8065 |
rs11212493 | snp | A/G | 0.135143 | 0.222054 | intron-variant | CUL5 | GRCh38.p7 | 11:108043664 | ATTGTTTTTCCTTCA[A/G]TTTCCCCATCTGTAA | 8065 |
rs11212494 | snp | A/C | 0 | 0 | intron-variant | CUL5 | GRCh38.p7 | 11:108044469 | gctgtgttcatgcca[A/C]tacacctcagactgg | 8065 |
rs11212495 | snp | A/G | 0.147656 | 0.228091 | intron-variant | CUL5 | GRCh38.p7 | 11:108048172 | TCTTCAGTTGAACAT[A/G]CCTTGTTAGGAAGGA | 8065 |
rs11212496 | snp | A/G | 0.0569829 | 0.158885 | intron-variant | CUL5 | GRCh38.p7 | 11:108051783 | ATTTCAAACACACCA[A/G]TATATCTGAAATTCA | 8065 |
rs11212497 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | CUL5 | GRCh38.p7 | 11:108052112 | ctgggactacaggca[A/C]atgccagcatgccta | 8065 |
rs11212498 | snp | A/G | 0.0592355 | 0.161582 | intron-variant | CUL5 | GRCh38.p7 | 11:108052339 | AGTTATTTTGAGACA[A/G]GGTCTTACTCTGTCA | 8065 |
rs11212499 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108054566 | TGCACATAATGACTC[C/T]TCAATATTTATTTCA | 8065 |
rs11212500 | snp | A/T | 0 | 0 | intron-variant | CUL5 | GRCh38.p7 | 11:108063656 | AAAATTAATAAAATT[A/T]AAAAAAAATAAATAA | 8065 |
rs11212501 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108064121 | ATCTTAGAAGAAAGA[C/T]TTTTAGTTTTTCTCC | 8065 |
rs11212502 | snp | A/C | 0 | 0 | intron-variant | CUL5 | GRCh38.p7 | 11:108064154 | TCAGTATGATACTAG[A/C]TACGGGTCTCTCATG | 8065 |
rs11212503 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108071468 | gagccccaccttgtt[G/T]cccaggctgatctcC | 8065 |
rs11212505 | snp | C/T | 0.456214 | 0.141336 | intron-variant | CUL5 | GRCh38.p7 | 11:108074569 | CAGCACTTTGGGAGG[C/T]CAGGGCGGGTGGATC | 8065 |
rs11212506 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108077647 | AAAAAAAAAAAAGAA[A/G]AAAAATCTCACTTGA | 8065 |
rs11212507 | snp | A/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108080593 | TAGAGATGGAGTTTC[A/T]CCATGTTGACCAGGA | 8065 |
rs11212508 | snp | A/T | 0.342806 | 0.232136 | intron-variant | CUL5 | GRCh38.p7 | 11:108085581 | TTAAAATGATAAATC[A/T]TTTTTACTCTTAGTA | 8065 |
rs11212509 | snp | C/T | 0.312104 | 0.242163 | intron-variant | CUL5 | GRCh38.p7 | 11:108086044 | AGATGGAAATTGTTA[C/T]CTGAGGAAAGAAAGT | 8065 |
rs11212510 | snp | A/G | 0.479014 | 0.100263 | intron-variant | CUL5 | GRCh38.p7 | 11:108093004 | GTATTTTTAGCAGAG[A/G]TGGGTTTCACCATGT | 8065 |
rs11212511 | snp | A/G | 0.142272 | 0.225598 | intron-variant | CUL5 | GRCh38.p7 | 11:108103285 | CTTAAAAGTGACTGG[A/G]CATCGTGGCTTACAC | 8065 |
rs11212512 | snp | A/T | 0.279991 | 0.248195 | utr-variant-3-prime, intron-variant | CUL5 | GRCh38.p7 | 11:108105388 | GTATTTTAAGGTCTC[A/T]TGATTAGGGATTTGT | 8065 |
rs11212513 | snp | C/T | 0.0166325 | 0.0896639 | utr-variant-3-prime, intron-variant | CUL5 | GRCh38.p7 | 11:108105896 | CTTTCAAGAGCATTT[C/T]GTAGGATCTGTCCCC | 8065 |
rs11302777 | in-del | -/T | 0.474091 | 0.11083 | intron-variant | CUL5 | GRCh38.p7 | 11:108098574 | TTAAAAAAACTTTAG[-/T]TTTTTTTTTTTTTTT | 8065 |
rs11385295 | in-del | -/C | 0.0543475 | 0.155628 | intron-variant | CUL5 | GRCh38.p7 | 11:108087770 | GAAGTTTGAGACCAG[-/C]CCTGGCCAACATGGC | 8065 |
rs11440201 | in-del | -/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108042219 | TTTTTTTTTTTTTTT[-/T]GAGACAGAGTCTTGC | 8065 |
rs11600706 | snp | C/G | 0.197703 | 0.244469 | intron-variant | CUL5 | GRCh38.p7 | 11:108017541 | TAATTAGGGCGGTAG[C/G]GAAAACAACGTGATA | 8065 |
rs11600740 | snp | A/G | 0.198634 | 0.244666 | intron-variant | CUL5 | GRCh38.p7 | 11:108017536 | ACTGGTAATTAGGGC[A/G]GTAGCGAAAACAACG | 8065 |
rs11602683 | snp | A/G | 0.168135 | 0.236216 | intron-variant | CUL5 | GRCh38.p7 | 11:108068900 | ACCTGCCTTACTACC[A/G]TTATACTGATCTTTA | 8065 |
rs11603079 | snp | A/G | 0.199254 | 0.244796 | intron-variant | CUL5 | GRCh38.p7 | 11:108057480 | atgctgacatacccc[A/G]tgatatgatgcacta | 8065 |
rs11604711 | snp | C/G | 0.144969 | 0.226867 | intron-variant | CUL5 | GRCh38.p7 | 11:108029872 | CTACTCTGGTACTCT[C/G]CACCTTTTATTTTTA | 8065 |
rs11605419 | snp | A/G | 0.198944 | 0.244731 | intron-variant | CUL5 | GRCh38.p7 | 11:108031311 | tagaggctatagtga[A/G]ccaagattatgccac | 8065 |
rs11605878 | snp | A/T | 0.196771 | 0.244268 | intron-variant | CUL5 | GRCh38.p7 | 11:108082830 | cagggtcttgctgtg[A/T]tgcccagtctggtct | 8065 |
rs11606820 | snp | G/T | 0.199564 | 0.24486 | intron-variant | CUL5 | GRCh38.p7 | 11:108100259 | TGAAGAAAATAACTT[G/T]AGGCTCGGCGCGGTG | 8065 |
rs11607509 | snp | A/C | 0 | 0 | intron-variant | CUL5 | GRCh38.p7 | 11:108040112 | TTCTATTTCCTCCCT[A/C]TCCTATTTCCCAACT | 8065 |
rs11607758 | snp | A/G | 0.197703 | 0.244469 | intron-variant | CUL5 | GRCh38.p7 | 11:108093220 | tgtgtaacttgacag[A/G]gtaagcatcttttct | 8065 |
rs11822270 | snp | C/T | 0.167484 | 0.23599 | intron-variant | CUL5 | GRCh38.p7 | 11:108086662 | ttttcaacttccaca[C/T]tcactcttttctaaa | 8065 |
rs11822609 | snp | A/T | 0.20111 | 0.245173 | intron-variant | CUL5 | GRCh38.p7 | 11:108047381 | GCTAGAATTTCTTAT[A/T]TTTTAGTTGGATCAT | 8065 |
rs11822651 | snp | C/G | 0.16618 | 0.23553 | intron-variant | CUL5 | GRCh38.p7 | 11:108091477 | gggcagatggcttgt[C/G]ctcagagtttgagat | 8065 |
rs11823929 | snp | A/C | 0.331874 | 0.236213 | intron-variant | CUL5 | GRCh38.p7 | 11:108015671 | GAGAGGGAATAGTGG[A/C]CTAATCAGTAACTGT | 8065 |
rs11824469 | snp | A/C/G | 0 | 0 | intron-variant | CUL5 | GRCh38.p7 | 11:108028867 | gacacttcttgctca[A/C/G]aatcttttaatggct | 8065 |
rs11825746 | snp | C/T | 0.198324 | 0.244601 | intron-variant | CUL5 | GRCh38.p7 | 11:108060729 | GTAATCTCAGCTACT[C/T]GGGAGGCTGAGGCAG | 8065 |
rs11826981 | snp | G/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108068171 | gatccgcccgcctta[G/T]cctcccaaagtgctg | 8065 |
rs11827637 | snp | C/G | 0.0535932 | 0.154675 | intron-variant | CUL5 | GRCh38.p7 | 11:108039482 | TTGAGAACTGCTGCT[C/G]TAGATCCatttacaa | 8065 |
rs11828176 | snp | A/G | 0.167158 | 0.235875 | intron-variant | CUL5 | GRCh38.p7 | 11:108069714 | CCTTAGTGCCTGCAC[A/G]TAGTAGGCATCCAAT | 8065 |
rs11828981 | snp | A/G | 0.0513262 | 0.151752 | intron-variant | CUL5 | GRCh38.p7 | 11:108011348 | CTTTGGTTCATATTA[A/G]TTAAGTACTTGTGGA | 8065 |
rs12049820 | snp | A/C | 0 | 0 | intron-variant | CUL5 | GRCh38.p7 | 11:108049432 | ctgtagcctcaactg[A/C]tggggctcaagcaat | 8065 |
rs12099038 | snp | C/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108045360 | attttgggaggctga[C/G]gcaggagaattgctt | 8065 |
rs12099180 | snp | A/G | 0.0528381 | 0.153711 | intron-variant | CUL5 | GRCh38.p7 | 11:108047372 | GAAGGCTAGGCTAGA[A/G]TTTCTTATTTTTTAG | 8065 |
rs12270224 | snp | A/G | 0.257176 | 0.249897 | intron-variant | CUL5 | GRCh38.p7 | 11:108053754 | gcgtgatcatggctc[A/G]ttgagcctccacctc | 8065 |
rs12270289 | snp | A/G | 0.0402882 | 0.136092 | intron-variant | CUL5 | GRCh38.p7 | 11:108053831 | ctgcaggcatgcacc[A/G]ccacacctggctaat | 8065 |
rs12272624 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108048362 | gcaatttgggctggt[C/T]tcagatgaatttgcc | 8065 |
rs12272676 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108048422 | gttggACATGGTGGT[C/T]TAAGAGAGCATTaaa | 8065 |
rs12273997 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CUL5 | GRCh38.p7 | 11:108048525 | agatgaaagtggaat[C/T]tacaatacctattca | 8065 |
rs12274005 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108048583 | tacatcggtggcatt[C/T]tgttggtcaaagtaa | 8065 |
rs12274053 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108048620 | ggaccagcccaaact[C/T]taatagtggggaaat | 8065 |
rs12276853 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | CUL5 | GRCh38.p7 | 11:108038057 | ACCTTGCTGCATACT[A/G]TCAATTAACTTATAC | 8065 |
rs12277112 | snp | C/T | 0 | 0 | intron-variant | CUL5 | GRCh38.p7 | 11:108096094 | gagtgagaactccgt[C/T]tgaaaaaaaaaaaaa | 8065 |
rs12277368 | snp | C/T | 0.258843 | 0.249844 | intron-variant | CUL5 | GRCh38.p7 | 11:108016548 | AGCTACCACCCCTAC[C/T]TGAGGTTTCTCTTAA | 8065 |
rs12277549 | snp | A/G | 0 | 0 | intron-variant | CUL5 | GRCh38.p7 | 11:108025806 | attctagtcacctca[A/G]ccttttcaaactctg | 8065 |
rs12279627 | snp | A/T | 0 | 0 | intron-variant | CUL5 | GRCh38.p7 | 11:108018247 | TTTGAGGAACACCTT[A/T]AAAAGGTTGCTGTGG | 8065 |
rs12284965 | snp | A/G | 0.0383715 | 0.133092 | intron-variant | CUL5 | GRCh38.p7 | 11:108059814 | gcttgaacccaggag[A/G]cggaggttgcagtaa | 8065 |
rs12284974 | snp | A/G | 0.0387552 | 0.1337 | intron-variant | CUL5 | GRCh38.p7 | 11:108059871 | cctgggtgacagagc[A/G]agactctgtctaaaa | 8065 |
rs12286340 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | CUL5 | GRCh38.p7 | 11:108100893 | aactagccaggtgta[A/G]tggtgcatgcctgtg | 8065 |
rs12286461 | snp | A/G | 0.0379877 | 0.132479 | intron-variant | CUL5 | GRCh38.p7 | 11:108066249 | tcaggaggctgaggc[A/G]ggagaaatggtgtga | 8065 |
rs12287660 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108019349 | AGTGGCTTCATAAAC[A/G]GTAAGGGAACCCACA | 8065 |
rs12289933 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108102874 | gatctcagcttactg[C/T]aacctccacctccca | 8065 |
rs12290028 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CUL5 | GRCh38.p7 | 11:108102826 | ATGCCttttgttttg[A/G]agacagggtctcagg | 8065 |
rs12292187 | snp | A/G | 0 | 0 | intron-variant | CUL5 | GRCh38.p7 | 11:108069458 | CCTATTTTAGGGCTT[A/G]TACTTACTTTACAGG | 8065 |
rs12293890 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108040312 | agtgagattccattt[C/T]tacaaaaaattagcc | 8065 |
rs12293999 | snp | C/G | 0.0134861 | 0.0810011 | intron-variant | CUL5 | GRCh38.p7 | 11:108010469 | TACTAAGAGGCAGTA[C/G]TGTATATCACCTTTT | 8065 |
rs12294084 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CUL5 | GRCh38.p7 | 11:108092525 | gtgataaaaaggaat[A/G]aactaataatacatg | 8065 |
rs12295056 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | CUL5 | GRCh38.p7 | 11:108036871 | ctgggaaatcctgac[C/T]ggaatgcaaggtgta | 8065 |
rs12365419 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | CUL5 | GRCh38.p7 | 11:108069439 | GTATTCCTAGAATAC[A/G]TAACCTATTTTAGGG | 8065 |
rs12416788 | snp | A/G | 0.141596 | 0.225274 | intron-variant | CUL5 | GRCh38.p7 | 11:108023586 | ACCCTTCGGGAGTCC[A/G]TGTACTACAGTTTAA | 8065 |
rs12417648 | snp | A/T | 0.251578 | 0.249995 | utr-variant-3-prime | CUL5 | GRCh38.p7 | 11:108106852 | AAAAAAAAAAAAAAA[A/T]TTTAATTTTTAAAAA | 8065 |
rs12418162 | snp | A/G | 0.115788 | 0.21092 | intron-variant | CUL5 | GRCh38.p7 | 11:108015265 | TAAAACCAGAATGAA[A/G]CAAGGGAGCAAGTCA | 8065 |
rs12418673 | snp | A/G | 0.25634 | 0.24992 | intron-variant | CUL5 | GRCh38.p7 | 11:108091805 | acagatggccaataa[A/G]tgcatgcaaagatac | 8065 |
rs12421312 | snp | A/G | 0.0562307 | 0.157967 | intron-variant | CUL5 | GRCh38.p7 | 11:108096829 | cctcggcctcccaaa[A/G]tgctgggattacagg | 8065 |
rs12421527 | snp | A/G | 0.143284 | 0.226079 | intron-variant | CUL5 | GRCh38.p7 | 11:108051785 | TTCAAACACACCAAT[A/G]TATCTGAAATTCAAC | 8065 |
rs12574572 | snp | C/T | 0.34526 | 0.23114 | intron-variant | CUL5 | GRCh38.p7 | 11:108048940 | aaagtgctgggatta[C/T]aggcatgagccaccg | 8065 |
rs12785296 | snp | G/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108041216 | TGTAGCCCATTTTCC[G/T]TCACAGGTGTTCCCT | 8065 |
rs12788061 | snp | C/T | 0.0592355 | 0.161582 | intron-variant | CUL5 | GRCh38.p7 | 11:108038485 | CTGAGGTCAGGAGTT[C/T]GAGACCAGCCTGGCC | 8065 |
rs12790410 | snp | A/T | 0.258288 | 0.249863 | intron-variant | CUL5 | GRCh38.p7 | 11:108099906 | TTAAACAAAAAAAAA[A/T]TTTTTTTTTTTTTTT | 8065 |
rs12792042 | snp | A/G | 0.323431 | 0.238972 | intron-variant | CUL5 | GRCh38.p7 | 11:108094535 | ATTTTATAATTACAT[A/G]TATATATTTTTTAAA | 8065 |
rs12793438 | snp | A/G | 0.138886 | 0.22395 | intron-variant | CUL5 | GRCh38.p7 | 11:108060336 | ATTACAGATATCCTT[A/G]TATGGTTAAGGGCCT | 8065 |
rs12794718 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | CUL5 | GRCh38.p7 | 11:108055182 | TTTGCCATACCTGTT[C/T]TAGACtttatttaat | 8065 |
rs12796482 | snp | C/T | 0.140242 | 0.224618 | intron-variant | CUL5 | GRCh38.p7 | 11:108085350 | aattttgcatgaata[C/T]ggttgtatgaggtat | 8065 |
rs12803043 | snp | C/T | 0.24932 | 0.249999 | intron-variant | CUL5 | GRCh38.p7 | 11:108010362 | GAAAATAATAGAAAA[C/T]ATACAGGAACCTAAC | 8065 |
rs12804351 | snp | G/T | 0 | 0 | intron-variant | CUL5 | GRCh38.p7 | 11:108035120 | gcaaactgtaaccaa[G/T]ccagaaaggcaaaca | 8065 |
rs12804831 | snp | A/G | 0.135143 | 0.222054 | intron-variant | CUL5 | GRCh38.p7 | 11:108067453 | ATACTGTTTATTTGT[A/G]CATATCTGAAACAAA | 8065 |
rs12808406 | snp | A/G | 0.391769 | 0.205917 | intron-variant | CUL5 | GRCh38.p7 | 11:108099129 | CCCACCTCTGCCTCC[A/G]GATTAGCTGGGACCA | 8065 |
rs13377275 | snp | A/C | 0.0193772 | 0.0965046 | intron-variant, utr-variant-3-prime | CUL5 | GRCh38.p7 | 11:108073966 | CATTTGTATTGCATA[A/C]CATCTTTTTCCATCC | 8065 |
rs17107660 | snp | A/G | 0.0803491 | 0.183626 | intron-variant | CUL5 | GRCh38.p7 | 11:108009611 | CCTGGCTGAGCGCTG[A/G]CGAGGAGCGATGCTT | 8065 |
rs17107675 | snp | G/T | 0.167158 | 0.235875 | intron-variant | CUL5 | GRCh38.p7 | 11:108030950 | TCACGTAGGTTGTTG[G/T]CAGATCATATGTTGA | 8065 |
rs17107678 | snp | G/T | 0.0509478 | 0.151255 | intron-variant | CUL5 | GRCh38.p7 | 11:108039936 | TAGAAGCATGTGATT[G/T]TCCTACTACTTGGAA | 8065 |
rs17107685 | snp | G/T | 0.247905 | 0.249991 | intron-variant | CUL5 | GRCh38.p7 | 11:108044142 | TGGACCAGATACCAT[G/T]ATCAAGCTGAATTGA | 8065 |
rs17107711 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | CUL5 | GRCh38.p7 | 11:108056774 | ATTAGGCAGACCAAG[C/T]AGAGTTACAGAAGTG | 8065 |
rs17107737 | snp | C/T | 0.0558544 | 0.157504 | intron-variant | CUL5 | GRCh38.p7 | 11:108094218 | GACCCCTTGTAATAC[C/T]GTATTTTGTTTCTAA | 8065 |
rs17616401 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | CUL5 | GRCh38.p7 | 11:108013547 | GTTACTTGTTGGCTC[A/G]CTAGCATGCCAGAGG | 8065 |
rs17617000 | snp | A/G | 0.0869089 | 0.189476 | intron-variant | CUL5 | GRCh38.p7 | 11:108053377 | AATGCATGGCACAAA[A/G]TCACTCTAGGTAGGT | 8065 |
rs17679325 | snp | A/G | 0.25801 | 0.249872 | intron-variant | CUL5 | GRCh38.p7 | 11:108068515 | TGTAGGAAGAACAGT[A/G]TAATGAATCCCCATT | 8065 |
rs34009874 | in-del | -/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108047492 | AAATTAAAACTGAGT[-/G]TTTTTCTATGTATGA | 8065 |
rs34044185 | in-del | -/A | 0.229429 | 0.249152 | intron-variant | CUL5 | GRCh38.p7 | 11:108031365 | ACGAGACTCTGTCTC[-/A]AAAAAAAAAAAAAAA | 8065 |
rs34048603 | in-del | -/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108082088 | CTTTTTATTTGTTTT[-/G]TTGTTTTTCTTTCAG | 8065 |
rs34057559 | in-del | -/T | 0.208474 | 0.246527 | intron-variant | CUL5 | GRCh38.p7 | 11:108082800 | ACCATGCCCGGCTAA[-/T]TTTTTTTTTTGAGAC | 8065 |
rs34112083 | in-del | -/T | 0.462034 | 0.132445 | intron-variant | CUL5 | GRCh38.p7 | 11:108020535 | GATTTTTTTTTTTTT[-/T]GTTTTTTGTTTAAAA | 8065 |
rs34130141 | in-del | -/A | | | intron-variant | CUL5 | GRCh38.p7 | 11:108018504 | AACCCCATCTCTACT[-/A]AAAAAAAAAAAAATA | 8065 |
rs34130496 | in-del | -/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108023020 | TGGGAGGCCAAGGCA[-/G]GGTGGATCACCTGAG | 8065 |
rs34169950 | in-del | -/A | | | intron-variant | CUL5 | GRCh38.p7 | 11:108093075 | CCGCCTCAGCCTCCC[-/A]AAAGTGCTGGGATTA | 8065 |
rs34248235 | in-del | -/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108095115 | AGCAGAAATAGTGAA[-/T]TTTTTTTCATGAAGT | 8065 |
rs34307674 | in-del | -/T | 0.0792508 | 0.182605 | intron-variant | CUL5 | GRCh38.p7 | 11:108049248 | GCCTTTTGTGACTAG[-/T]TTTCTTTCACAATAT | 8065 |
rs34312194 | in-del | -/T | 0 | 0 | intron-variant | CUL5 | GRCh38.p7 | 11:108012540 | TATGTCCCCTCTTAC[-/T]TTTTTTTTTTTTTTT | 8065 |
rs34341366 | in-del | -/A | | | utr-variant-3-prime | CUL5 | GRCh38.p7 | 11:108106614 | AATCATTTAGTTGAC[-/A]AGGTGCCTATGCCAT | 8065 |
rs34344819 | in-del | -/A | 0.44546 | 0.155869 | downstream-variant-500B | CUL5 | GRCh38.p7 | 11:108108013 | CCTGGAAGAGGTAAT[-/A]AAAAAAAAAAAATTC | 8065 |
rs34367275 | in-del | -/T | | | intron-variant, downstream-variant-500B | CUL5 | GRCh38.p7 | 11:108074191 | TTTTGTCTATTTTAA[-/T]TTTTTTTTTTTTTTT | 8065 |
rs34480816 | in-del | -/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108068736 | AAGAGAAGTAAATAA[-/T]TTACATGACACGAGG | 8065 |
rs34514310 | in-del | -/T | 0.0569829 | 0.158885 | intron-variant | CUL5 | GRCh38.p7 | 11:108070624 | AAGATTTCTAAAGGA[-/T]TTTTTTTATTACTTC | 8065 |
rs34573702 | snp | G/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108041299 | TCTTTTTTTTTTTTT[G/T]GAGACGGAGTCTCTG | 8065 |
rs34584659 | in-del | -/A | | | utr-variant-3-prime | CUL5 | GRCh38.p7 | 11:108106575 | GTATACAAAAGTTTT[-/A]AACTACTTTTTGGTG | 8065 |
rs34618859 | in-del | -/T | 0.439918 | 0.162576 | intron-variant | CUL5 | GRCh38.p7 | 11:108080112 | GAGCAATTTTTCATC[-/T]TTTTTTTTTTTTTTT | 8065 |
rs34637571 | in-del | -/AA | 0.376592 | 0.215579 | intron-variant | CUL5 | GRCh38.p7 | 11:108077612 | TGCAGCCTGGGCAAC[-/AA]GAGTGAAACTCTGTC | 8065 |
rs34667046 | in-del | -/C | | | intron-variant | CUL5 | GRCh38.p7 | 11:108070592 | AATAGTCATCTCTGT[-/C]CCCCAAAAATACTTT | 8065 |
rs34730838 | in-del | -/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108062038 | CCTGTCTCAACACGT[-/G]GGGAATTACAATTCG | 8065 |
rs34738907 | in-del | -/A | | | intron-variant | CUL5 | GRCh38.p7 | 11:108029762 | ATTATGTGTTCCATC[-/A]AAAAGGAGAGCAAAA | 8065 |
rs34756428 | in-del | -/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108059365 | ACACTAGAATAAAAT[-/G]GGATTGTTTATACAA | 8065 |
rs34792578 | in-del | -/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108062068 | AGATGAAATTTGGCT[-/G]GGGGATACAGAGCCA | 8065 |
rs34832948 | in-del | -/C | | | intron-variant | CUL5 | GRCh38.p7 | 11:108094267 | TTAGACAATAAAATT[-/C]CTAATAAATGAGAAA | 8065 |
rs34850383 | in-del | -/C | | | intron-variant | CUL5 | GRCh38.p7 | 11:108019701 | TATACAGTACATAAT[-/C]CCTTGGATAATAGGA | 8065 |
rs34885188 | in-del | -/C | | | intron-variant | CUL5 | GRCh38.p7 | 11:108019494 | TGATGTTTTGGTCAA[-/C]CAACGGATCACATAT | 8065 |
rs34900148 | in-del | -/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108031546 | ACCATTTATTGAACA[-/G]GGGAGTCCTTTCTCT | 8065 |
rs34934731 | in-del | -/C | | | intron-variant | CUL5 | GRCh38.p7 | 11:108043181 | AGTTCAAGTGATCTT[-/C]CCCTCAGCCTCCTGA | 8065 |
rs34941469 | in-del | -/A | 0.421684 | 0.181726 | intron-variant | CUL5 | GRCh38.p7 | 11:108026989 | GTGAGACTCCGTCTC[-/A]AAAAAAAAAAAAAAA | 8065 |
rs34957608 | in-del | -/C | | | intron-variant | CUL5 | GRCh38.p7 | 11:108054533 | ATAATTATATGTTCT[-/C]CTTGAGCATTGTTAC | 8065 |
rs34995865 | in-del | -/C | | | intron-variant | CUL5 | GRCh38.p7 | 11:108093256 | TGGAGAGTTGTCACA[-/C]CCCCCTGTAATTTGG | 8065 |
rs35036425 | in-del | -/A | 0.188 | 0.24219 | intron-variant | CUL5 | GRCh38.p7 | 11:108059883 | AGCGAGACTCTGTCT[-/A]AAAAAAAAAAAAAAA | 8065 |
rs35046631 | in-del | -/A | | | intron-variant | CUL5 | GRCh38.p7 | 11:108030196 | TCTGACTCTGAATTT[-/A]CCCAGTAGCCAACAC | 8065 |
rs35066482 | in-del | -/A | | | intron-variant | CUL5 | GRCh38.p7 | 11:108070691 | AGTATATAACAAACT[-/A]AAAAAAAAAAATTGT | 8065 |
rs35086457 | in-del | -/T/TT/TTT | 0.464416 | 0.128553 | intron-variant | CUL5 | GRCh38.p7 | 11:108099005 | TTCTGGCCAGTGTAC[-/T/TT/TTT]TTTTTTTTTTTTTTT | 8065 |
rs35093716 | in-del | -/A | | | utr-variant-3-prime | CUL5 | GRCh38.p7 | 11:108106567 | TTTGGTTATGTATAC[-/A]AAAGTTTTAACTACT | 8065 |
rs35135984 | in-del | -/A | | | intron-variant | CUL5 | GRCh38.p7 | 11:108044508 | GTGAGACAGTGTCTC[-/A]AAAAAAAAAAAATTA | 8065 |
rs35165456 | in-del | -/TTGGTCTCCCAAA | | | intron-variant | CUL5 | GRCh38.p7 | 11:108022095 | GTGATCCTCCCACCG[-/TTGGTCTCCCAAA]TGCTGGAATTATAGG | 8065 |
rs35185677 | snp | A/C | | | intron-variant | CUL5 | GRCh38.p7 | 11:108103381 | CCTGGACAACATAGC[A/C]AAACCTTGTGTCTGT | 8065 |
rs35185685 | snp | A/G | 0.145978 | 0.227331 | intron-variant | CUL5 | GRCh38.p7 | 11:108037660 | TCTACCAGGGAAGCT[A/G]ATTAGGGGCTCAGCA | 8065 |
rs35194811 | in-del | -/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108047780 | GTTTCTACTTGCATT[-/G]GGGAAATGTACCACG | 8065 |
rs35209870 | in-del | -/T | 0.277334 | 0.248501 | upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108008530 | ATTCTCTAAACAATC[-/T]TTTTTTTTTTTTTTC | 8065 |
rs35226384 | in-del | -/C | | | intron-variant | CUL5 | GRCh38.p7 | 11:108076321 | TACAGGCATGAGCCA[-/C]CCATGCCCAGCCCAG | 8065 |
rs35237843 | snp | C/T | 0.143284 | 0.226079 | intron-variant | CUL5 | GRCh38.p7 | 11:108077030 | ATGGAGCTGGAAAAA[C/T]ATGTTTGGCAGCTTC | 8065 |
rs35289099 | in-del | -/A | 0.498754 | 0.0249289 | intron-variant | CUL5 | GRCh38.p7 | 11:108077630 | TGAAACTCTGTCTCC[-/A]AAAAAAAAAAAAAGA | 8065 |
rs35324496 | in-del | -/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108088684 | TTTTTGTATTTCAAC[-/T]TTTTAAAATTACCTT | 8065 |
rs35325107 | snp | A/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108038866 | TTAGTTACTAAATAA[A/T]GTATTGATGTTAAGG | 8065 |
rs35375054 | in-del | -/A | 0.392696 | 0.205275 | intron-variant | CUL5 | GRCh38.p7 | 11:108090039 | ATTTCAAAAAAAAAA[-/A]GAATATACCATCAAT | 8065 |
rs35431519 | in-del | -/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108044064 | CACATGATAAGCAGT[-/G]CAGGTGTTACCTTTT | 8065 |
rs35438479 | in-del | -/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108010792 | GCAAATTTCTCATGC[-/T]TTTACTTCAGAAAGA | 8065 |
rs35447216 | in-del | -/C | 0.00358779 | 0.0422022 | intron-variant | CUL5 | GRCh38.p7 | 11:108096372 | GCTTGGTGGCTGTAT[-/C]CCCCAGCTACTTGGA | 8065 |
rs35451351 | snp | G/T | | | utr-variant-3-prime | CUL5 | GRCh38.p7 | 11:108106554 | TTTTTTTTTTTTTTT[G/T]GGTTATGTATACAAA | 8065 |
rs35581482 | in-del | -/T | 0.249038 | 0.249998 | intron-variant | CUL5 | GRCh38.p7 | 11:108027274 | ACCATGCCCAGCTAA[-/T]TTTTTTTTTTTTTCT | 8065 |
rs35583347 | snp | A/C | 0.279726 | 0.248226 | intron-variant | CUL5 | GRCh38.p7 | 11:108068441 | CTCCCACCTCAGCCC[A/C]CCAACTCGCAGGGAC | 8065 |
rs35624225 | in-del | -/A | | | intron-variant | CUL5 | GRCh38.p7 | 11:108022851 | CAAGACCCCATCTCT[-/A]AAAAAAAGTCAATTA | 8065 |
rs35762917 | in-del | -/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108075209 | TTTTTTTTTTTTAAT[-/G]GCAAGTAGCTTATTT | 8065 |
rs35833167 | in-del | -/A | 0.375 | 0.216506 | intron-variant | CUL5 | GRCh38.p7 | 11:108035591 | GAGACCCTGTCTCTT[-/A]AAAAAAAAAAAAAAA | 8065 |
rs35834569 | in-del | -/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108076453 | TTTCTTTCCCACCCA[-/T]TTTTGCCACTGGTAC | 8065 |
rs35844502 | in-del | -/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108053679 | AGTGGTATACCATGC[-/T]TTTTTTTTTTTTTTT | 8065 |
rs35860055 | snp | C/G | 0.391954 | 0.205789 | intron-variant | CUL5 | GRCh38.p7 | 11:108099220 | ATGTTGCCCAGGCTG[C/G]TCTCGAACTCCTGGG | 8065 |
rs35888900 | in-del | -/C | | | intron-variant | CUL5 | GRCh38.p7 | 11:108052559 | AGCCACTGCACCTGG[-/C]CCCAGGCCTACAAAT | 8065 |
rs35892865 | in-del | -/C | | | intron-variant | CUL5 | GRCh38.p7 | 11:108101920 | AACCCCTGACATAAA[-/C]CCCCAATTTATGATG | 8065 |
rs35920881 | in-del | -/G | | | intron-variant, utr-variant-3-prime | CUL5 | GRCh38.p7 | 11:108073944 | TATCCTTGTTTCCCA[-/G]GGGAAGCATTTGTAT | 8065 |
rs35921693 | in-del | -/T | 0.257732 | 0.24988 | intron-variant | CUL5 | GRCh38.p7 | 11:108062221 | ATCCTTAAATACCTC[-/T]TATCTTTTTAACATC | 8065 |
rs35939930 | in-del | -/A | 0.472803 | 0.113397 | intron-variant | CUL5 | GRCh38.p7 | 11:108091367 | TGTTATTTCTTTGTT[-/A]AAAAAAAAAATATCA | 8065 |
rs35973307 | in-del | -/TA | | | intron-variant | CUL5 | GRCh38.p7 | 11:108088069 | TTTAATGCATGATGG[-/TA]TATATATATCATCAT | 8065 |
rs36034326 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant, upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108033092 | ATTTGTTATAGGGAA[A/G]GGATTCAGATAAAAT | 8065 |
rs55641462 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108029182 | GTGAAGGGATTAGTT[A/G]TGCTGTAAGGAGTGA | 8065 |
rs55661520 | in-del | -/AATA | 0 | 0 | intron-variant | CUL5 | GRCh38.p7 | 11:108063674 | AAAAATAAATAAATA[-/AATA]GTGCTGCAGTAAACG | 8065 |
rs55781012 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108029172 | AAGAGTGCCTGTGAA[A/G]GGATTAGTTGTGCTG | 8065 |
rs55837255 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | CUL5 | GRCh38.p7 | 11:108018592 | AGGCAGGAGAATCAC[C/T]TGAACCCACGAGGCA | 8065 |
rs55864212 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108029146 | TCCCCACGGCCCATT[C/T]GTGTGAGAAGAAGAG | 8065 |
rs56014421 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | CUL5 | GRCh38.p7 | 11:108059679 | GTCAGGAGTTCAAGA[C/T]CAGCCTGGCCAACAC | 8065 |
rs56180540 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | CUL5 | GRCh38.p7 | 11:108048901 | CAAACTCATGACCTC[A/G]TGATCTGCCCGCCTT | 8065 |
rs56214765 | snp | A/G | 0.236724 | 0.249647 | intron-variant | CUL5 | GRCh38.p7 | 11:108041764 | CCTGGCTAATTTTTC[A/G]TATTTTTAGTGGAGA | 8065 |
rs56321753 | snp | G/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108102541 | TCGCCATGTTGCCTA[G/T]GCTGGTCTCAAACTC | 8065 |
rs56695504 | snp | G/T | 0.0193772 | 0.0965046 | intron-variant | CUL5 | GRCh38.p7 | 11:108025880 | GGTTTCCCCTCCTTG[G/T]GATGAGGCCTGGAGA | 8065 |
rs56699789 | in-del | -/A | | | intron-variant | CUL5 | GRCh38.p7 | 11:108038125 | GCTGAGGCCTTTTAA[-/A]GCTTTATTACATTCA | 8065 |
rs56989053 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108095804 | AGAATGTCTTATCAA[A/G]AAAAATAGAGGCCGG | 8065 |
rs57114718 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108028696 | CAAAAATTAGCTGAG[C/T]GTGGTGGTGCACACC | 8065 |
rs57684783 | in-del | -/T/TT | 0.5 | 0 | intron-variant | CUL5 | GRCh38.p7 | 11:108020548 | GATTTTTTTTTTTTT[-/T/TT]GTTTTTTGTTTAAAA | 8065 |
rs58243661 | snp | C/T | 0.198014 | 0.244535 | intron-variant | CUL5 | GRCh38.p7 | 11:108051563 | TAACTCTTGTTGTTA[C/T]TGTTGCTGTCATTAA | 8065 |
rs58440704 | snp | C/T | 0.0364509 | 0.129988 | intron-variant | CUL5 | GRCh38.p7 | 11:108099095 | CTGCAGCCTCAACTC[C/T]CTGGGCTCAAAGGAT | 8065 |
rs58512172 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | CUL5 | GRCh38.p7 | 11:108024762 | TAATCCCCAATTAGT[G/T]AAATGCCATATATTT | 8065 |
rs59000049 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108018020 | GCTTTTCTTAAAAGT[A/C]TGGTTATTCCAAATT | 8065 |
rs59142867 | in-del | -/A | | | intron-variant | CUL5 | GRCh38.p7 | 11:108016797 | TGTACAAAAACAAAC[-/A]AAAAAAAAACAAACA | 8065 |
rs60684284 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108096730 | TGCCACCACACTCAG[C/T]TAATTTTATATTTTT | 8065 |
rs60762047 | snp | A/G | 0.116138 | 0.211142 | intron-variant | CUL5 | GRCh38.p7 | 11:108100623 | AAGGAAATAATTTCT[A/G]TGACCTATGGAAAGA | 8065 |
rs60875534 | snp | A/G | 0.0236746 | 0.106192 | intron-variant | CUL5 | GRCh38.p7 | 11:108078110 | TTTATGTGTTTTGGG[A/G]TGTATAAAAATTTAT | 8065 |
rs61163942 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | CUL5 | GRCh38.p7 | 11:108014960 | CTGGAGTGCAGTGGC[A/G]CGATCTTGGCTCACT | 8065 |
rs61324649 | in-del | -/A | | | intron-variant | CUL5 | GRCh38.p7 | 11:108066353 | GTCTCAAAAAAAAAA[-/A]CCAGAGTATCATTAT | 8065 |
rs61420788 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | CUL5 | GRCh38.p7 | 11:108029856 | TATCTCCAGTACCTG[C/T]CTACTCTGGTACTCT | 8065 |
rs61676080 | in-del | -/TTGGTCTCCCAAA | 0.447032 | 0.153878 | intron-variant | CUL5 | GRCh38.p7 | 11:108022094 | AGTGATCCTCCCACC[-/TTGGTCTCCCAAA]GTGCTGGAATTATAG | 8065 |
rs61909311 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108011696 | TCAGTGGTGCGATCT[C/T]GGTTCACTGCAACTT | 8065 |
rs61909312 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108011699 | GTGGTGCGATCTTGG[C/T]TCACTGCAACTTCCG | 8065 |
rs61914360 | snp | C/G | 0.0333695 | 0.124785 | intron-variant, upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108032183 | AAAGTTAAAGAAAAT[C/G]GTGACTTTTGTTGAA | 8065 |
rs61914361 | snp | A/G | 0.0333695 | 0.124785 | intron-variant | CUL5 | GRCh38.p7 | 11:108034187 | ATGGGGTGAAGTGCA[A/G]GAAAAAACAAGCACA | 8065 |
rs61914362 | snp | A/G | 0 | 0 | intron-variant | CUL5 | GRCh38.p7 | 11:108043059 | TGAGCCGCCATGCCC[A/G]GCCTGTTTCTTTTTT | 8065 |
rs61914387 | snp | A/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108048116 | TTTTAAACGCTTAAG[A/T]AATTTTTTTTTTTTT | 8065 |
rs61914388 | snp | C/T | 0.0333695 | 0.124785 | intron-variant | CUL5 | GRCh38.p7 | 11:108071407 | AGCTGGGACTACAGC[C/T]GTGTACCACCATGCC | 8065 |
rs61914389 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | CUL5 | GRCh38.p7 | 11:108086698 | ACCCTGTGATGGAAG[C/T]ATCACAGCAGTTTTT | 8065 |
rs61914390 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108100044 | ATATTAATATCAAGT[C/T]CAAAATTTTAAAATT | 8065 |
rs61916871 | snp | A/G | 0.188631 | 0.242351 | intron-variant | CUL5 | GRCh38.p7 | 11:108019143 | TAATAAGCAAATGCT[A/G]TGCCATTTTCTATCA | 8065 |
rs61916872 | snp | A/T | 0.5 | 0 | intron-variant | CUL5 | GRCh38.p7 | 11:108027272 | CCACCATGCCCAGCT[A/T]ATTTTTTTTTTTTTT | 8065 |
rs66652829 | in-del | -/TTAT | 0.5 | 0 | intron-variant | CUL5 | GRCh38.p7 | 11:108021823 | GCCCAGTTTATTTAT[-/TTAT]TTTTCAGAGACAGGG | 8065 |
rs67141256 | in-del | -/A | 0.108048 | 0.20579 | utr-variant-3-prime | CUL5 | GRCh38.p7 | 11:108106539 | AAAAAAAAAAAAAAA[-/A]GAAAACTGTACATTT | 8065 |
rs67456286 | snp | G/T | 0.255224 | 0.249945 | intron-variant | CUL5 | GRCh38.p7 | 11:108076570 | CTGGCTTATTTTTAA[G/T]GTCTTCCAGGCTTCC | 8065 |
rs67606910 | in-del | -/ATGAA | 0.465368 | 0.126951 | intron-variant | CUL5 | GRCh38.p7 | 11:108067475 | TGAAACAAAAGTCTT[-/ATGAA]ATAATATTCATTGTT | 8065 |
rs68076088 | snp | G/T | 0.351418 | 0.228505 | intron-variant | CUL5 | GRCh38.p7 | 11:108079659 | TGTACATTTGAGTCA[G/T]ATTTGACAAATGCCT | 8065 |
rs68126927 | in-del | -/A | 0 | 0 | intron-variant | CUL5 | GRCh38.p7 | 11:108063656 | TTATTTATTTTTTTT[-/A]AATTTTATTAATTTT | 8065 |
rs71047666 | in-del | -/T | 0 | 0 | intron-variant | CUL5 | GRCh38.p7 | 11:108023552 | AGGATATATTCTTTG[-/T]TTTTTTTTCTTTTTT | 8065 |
rs71047667 | in-del | -/TTTT | 0 | 0 | intron-variant | CUL5 | GRCh38.p7 | 11:108040635 | ACCACGACTGGCTAA[-/TTTT]TTTTTTTTTTTTTTT | 8065 |
rs71047670 | in-del | -/T | 0 | 0 | intron-variant | CUL5 | GRCh38.p7 | 11:108096335 | AAGCTGGCTAATTTG[-/T]TTTTTTTTTTTTTTT | 8065 |
rs71047671 | in-del | -/A | 0 | 0 | intron-variant | CUL5 | GRCh38.p7 | 11:108096591 | CGACAAGAGTGTTTC[-/A]AAAAAAAAAAAAAAA | 8065 |
rs71303233 | in-del | -/GTGTGTGTGT/TTGT/TTGTGTGTGT | 0.5 | 0 | intron-variant | CUL5 | GRCh38.p7 | 11:108091732 | TTTTAATTATTTGTC[-/GTGTGTGTGT/TTGT/TTGTGTGTGT]GTGTGTGTGTGTGTG | 8065 |
rs71464788 | snp | A/T | 0.116488 | 0.211364 | intron-variant | CUL5 | GRCh38.p7 | 11:108100351 | AGTTCAAGACCAGCC[A/T]AGCCAACATGTTGAA | 8065 |
rs71476009 | in-del | -/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108038229 | TTTGTTGTTAATGTT[-/G]TTTTTGCCAGTCTGT | 8065 |
rs71476010 | in-del | -/A | 0.5 | 0 | intron-variant | CUL5 | GRCh38.p7 | 11:108057926 | GAAAAAATAAAGAAT[-/A]TTGGCTGGGTGCAGT | 8065 |
rs71476011 | in-del | -/G | 0.5 | 0 | intron-variant | CUL5 | GRCh38.p7 | 11:108077669 | TCACTTGAGGCCAGG[-/G]CATGGTGGCTCACCC | 8065 |
rs71476012 | in-del | -/AATTA | 0.5 | 0 | intron-variant | CUL5 | GRCh38.p7 | 11:108078403 | TATAATTTTTTATTA[-/AATTA]TTTTACAATACAAAA | 8065 |
rs71488289 | snp | A/C | 0.5 | 0 | intron-variant | CUL5 | GRCh38.p7 | 11:108018701 | AGAGAGAGAAACATC[A/C]CATATATGCACTTAA | 8065 |
rs71488290 | snp | A/C | 0.5 | 0 | intron-variant | CUL5 | GRCh38.p7 | 11:108077955 | CTTCATCTCAAAAAA[A/C]CAAAACCAAACCAAC | 8065 |
rs71488291 | snp | A/G | 0.0267878 | 0.112589 | intron-variant | CUL5 | GRCh38.p7 | 11:108094663 | TCAAAGCAGTGTGTT[A/G]GATTTACAGATCTTT | 8065 |
rs71840119 | in-del | -/A | | | intron-variant | CUL5 | GRCh38.p7 | 11:108017410 | AAAAAAAAAAAAAAA[-/A]GTATCAGTGATACAA | 8065 |
rs72351550 | in-del | -/TTTA | 0.140581 | 0.224783 | intron-variant | CUL5 | GRCh38.p7 | 11:108021814 | AGCCACACCGCCCAG[-/TTTA]TTTATTTATTTTTCA | 8065 |
rs72392553 | in-del | -/TGT | 0.144969 | 0.226867 | intron-variant | CUL5 | GRCh38.p7 | 11:108038225 | GTGTTTTGTTGTTAA[-/TGT]TGTTTTTGCCAGTCT | 8065 |
rs72414665 | in-del | -/TT | | | intron-variant | CUL5 | GRCh38.p7 | 11:108012524 | TATGTCCCCTCTTAC[-/TT]TTTTTTTTTTTTTTT | 8065 |
rs72996476 | snp | A/G | 0.0252325 | 0.109451 | intron-variant | CUL5 | GRCh38.p7 | 11:108037983 | TGTACACATTGGGCT[A/G]TTGTAATCGTTTTCT | 8065 |
rs72996480 | snp | C/T | 0.247905 | 0.249991 | intron-variant | CUL5 | GRCh38.p7 | 11:108039356 | GTCATGAACACTCCT[C/T]CTGTGTCTTTCTCCT | 8065 |
rs72996483 | snp | A/G | 0.0829062 | 0.185956 | intron-variant | CUL5 | GRCh38.p7 | 11:108039926 | TGGTCTTAGTTAGAA[A/G]CATGTGATTGTCCTA | 8065 |
rs72996496 | snp | A/G | 0.0829062 | 0.185956 | intron-variant | CUL5 | GRCh38.p7 | 11:108049647 | ACGCCTGGCCCATAT[A/G]TTGTTTATCCGTATT | 8065 |
rs72998471 | snp | A/G | 0.0832709 | 0.186283 | intron-variant | CUL5 | GRCh38.p7 | 11:108059313 | GCATTATGCTAGTTG[A/G]GGATAATAAGATAGA | 8065 |
rs72998495 | snp | A/G | 0.0298908 | 0.118541 | intron-variant | CUL5 | GRCh38.p7 | 11:108069819 | AGGAAGAGTTAATCA[A/G]AGTTTGGTTTTGTAT | 8065 |
rs73000508 | snp | C/T | 0.084728 | 0.187577 | intron-variant | CUL5 | GRCh38.p7 | 11:108076332 | AGCCACCATGCCCAG[C/T]CCAGTATAATTTTAC | 8065 |
rs73000512 | snp | A/G | 0.0803491 | 0.183626 | intron-variant | CUL5 | GRCh38.p7 | 11:108078659 | CTAAGCCTAGCTTAT[A/G]GAAAATCTGACAACT | 8065 |
rs73000522 | snp | C/T | 0.0825414 | 0.185628 | intron-variant | CUL5 | GRCh38.p7 | 11:108095313 | TTTTCCATTTGCATC[C/T]GCCAGTACTCAGTCA | 8065 |
rs73000527 | snp | A/T | 0.117688 | 0.212117 | intron-variant | CUL5 | GRCh38.p7 | 11:108097793 | ATAAAAACACCTTGT[A/T]TGAATTTTAGCACTT | 8065 |
rs73000534 | snp | C/T | 0.0836354 | 0.186609 | intron-variant | CUL5 | GRCh38.p7 | 11:108100038 | TTTCTGATATTAATA[C/T]CAAGTTCAAAATTTT | 8065 |
rs73000537 | snp | A/G | 0.0836354 | 0.186609 | intron-variant | CUL5 | GRCh38.p7 | 11:108100260 | GAAGAAAATAACTTT[A/G]GGCTCGGCGCGGTGG | 8065 |
rs73000543 | snp | A/T | 0.029116 | 0.117091 | utr-variant-3-prime, intron-variant | CUL5 | GRCh38.p7 | 11:108105699 | TGAAAGAGAAAATTG[A/T]TTCCCCTTGAGGAAA | 8065 |
rs73000548 | snp | G/T | 0.040671 | 0.13668 | utr-variant-3-prime | CUL5 | GRCh38.p7 | 11:108107422 | CAAGCTGGTTTTTCT[G/T]TTCTCATGTAAGTGA | 8065 |
rs73555364 | snp | A/G | 0.0368353 | 0.130617 | intron-variant | CUL5 | GRCh38.p7 | 11:108009566 | CAGGCTCTGGTGGTC[A/G]CTCCCGCCGACTGGC | 8065 |
rs73555365 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108009771 | AAGAAAATGCTGCCT[A/G]ACAGGTTTCAGTGAC | 8065 |
rs73555370 | snp | A/G/T | 0.0236746 | 0.106192 | intron-variant | CUL5 | GRCh38.p7 | 11:108018311 | GGTATTCAAATATAT[A/G/T]CAATCAGCCCTCAGT | 8065 |
rs73555372 | snp | C/T | 0.198014 | 0.244535 | intron-variant | CUL5 | GRCh38.p7 | 11:108019613 | CAATAACACATCACT[C/T]GTGTCTGTGGCGATG | 8065 |
rs73555373 | snp | A/G | 0.0364509 | 0.129988 | intron-variant | CUL5 | GRCh38.p7 | 11:108022013 | ACCTATCTATCCATC[A/G]ATCCATCCATTCTTA | 8065 |
rs73555376 | snp | A/T | 0.0364509 | 0.129988 | intron-variant | CUL5 | GRCh38.p7 | 11:108022893 | TGTTTTGCTTTTCTT[A/T]TGGACTTTTTAGTTC | 8065 |
rs73555378 | snp | G/T | 0.0364509 | 0.129988 | intron-variant | CUL5 | GRCh38.p7 | 11:108024542 | AACATGTAACAGTCA[G/T]ATATTATAAAGTAAA | 8065 |
rs73555391 | snp | A/G | 0.197393 | 0.244402 | intron-variant | CUL5 | GRCh38.p7 | 11:108042004 | AACTAAATAAAAGAT[A/G]ATGGGGACTATCATG | 8065 |
rs73555392 | snp | A/G | 0.0236746 | 0.106192 | intron-variant | CUL5 | GRCh38.p7 | 11:108042353 | CCTCCCAAATTGCTG[A/G]GACAACAGGCGTGCC | 8065 |
rs73555397 | snp | C/T | 0.0236746 | 0.106192 | intron-variant | CUL5 | GRCh38.p7 | 11:108051036 | AGTCAATTTACTGTT[C/T]ACTGTGATGGTTACA | 8065 |
rs73557106 | snp | A/T | 0.197082 | 0.244335 | intron-variant | CUL5 | GRCh38.p7 | 11:108055618 | CCTGACTAATAAATA[A/T]ATATATATATATACT | 8065 |
rs73557111 | snp | A/T | 0.198014 | 0.244535 | intron-variant | CUL5 | GRCh38.p7 | 11:108055943 | GCCACCTGGCTAATT[A/T]TTTTATTTTATTTTT | 8065 |
rs73557117 | snp | A/C | 0.0368353 | 0.130617 | intron-variant | CUL5 | GRCh38.p7 | 11:108060841 | CTCAAAAAAAAAAAG[A/C]ATAAGAATCTACCAT | 8065 |
rs73557122 | snp | C/T | 0.198634 | 0.244666 | intron-variant | CUL5 | GRCh38.p7 | 11:108063841 | CTTGTACTAATATTA[C/T]ATTCCCACCATCATT | 8065 |
rs73557129 | snp | C/T | 0.0236746 | 0.106192 | intron-variant | CUL5 | GRCh38.p7 | 11:108067358 | CTCAGTTTACTTTAA[C/T]TATGTTGTCAATTTA | 8065 |
rs73557135 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | CUL5 | GRCh38.p7 | 11:108068934 | ATGACTTGAGGAGAG[A/G]AGAATCTCATTACAT | 8065 |
rs73557142 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | CUL5 | GRCh38.p7 | 11:108072128 | AGGCTGCAGTGAGCC[A/G]TGATCGAGCCACTGT | 8065 |
rs73557152 | snp | A/G | 0.0368353 | 0.130617 | intron-variant | CUL5 | GRCh38.p7 | 11:108077831 | GCACCTATAATCCCA[A/G]CTACCCAGGAGGCCA | 8065 |
rs73557155 | snp | C/T | 0.197082 | 0.244335 | intron-variant | CUL5 | GRCh38.p7 | 11:108079740 | ATGTCTATTCCCAGT[C/T]GGTCCCACCCCACCT | 8065 |
rs73557160 | snp | A/G | 0.0364509 | 0.129988 | intron-variant | CUL5 | GRCh38.p7 | 11:108082905 | GTGCCAGAATTACAG[A/G]CATGAGCTACCATGC | 8065 |
rs73557162 | snp | A/G | 0.0368353 | 0.130617 | intron-variant | CUL5 | GRCh38.p7 | 11:108085504 | CTAGAAATAGATAGC[A/G]GTGATGTTTGTACAG | 8065 |
rs73557165 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | CUL5 | GRCh38.p7 | 11:108088242 | AAAATTTTAATTATC[A/G]TTGCCAAGGTCAGCA | 8065 |
rs73557174 | snp | C/G | 0.0364509 | 0.129988 | intron-variant | CUL5 | GRCh38.p7 | 11:108092035 | CTAGCTACTCAGGAG[C/G]CTGAGATGGGATGAT | 8065 |
rs73557188 | snp | C/T | 0.202959 | 0.245534 | intron-variant | CUL5 | GRCh38.p7 | 11:108098811 | AAATTAGGAAACTTA[C/T]TTAGAACCAAAAAAG | 8065 |
rs73557192 | snp | C/G | 0.0364509 | 0.129988 | intron-variant | CUL5 | GRCh38.p7 | 11:108099334 | AAATATAAAACAAGA[C/G]GAAAAGATTAAAAAT | 8065 |
rs74333671 | snp | C/T | 0.0543475 | 0.155628 | intron-variant | CUL5 | GRCh38.p7 | 11:108019876 | GGTGAGGTCCTCAGC[C/T]TGCTTCTACTCATGG | 8065 |
rs74348837 | snp | C/G | 0.5 | 0 | intron-variant | CUL5 | GRCh38.p7 | 11:108081373 | GCTTTTGTATATGGT[C/G]TGAGATACAGCTCTA | 8065 |
rs74461546 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | CUL5 | GRCh38.p7 | 11:108085628 | AAAGGAATGAACTAC[G/T]GGTACATGCTGTGAC | 8065 |
rs74504952 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108087012 | TGGTAGATGTTAGCC[A/G]TTCTTTAAAGATGGA | 8065 |
rs74509423 | snp | A/G | 0.0252325 | 0.109451 | intron-variant | CUL5 | GRCh38.p7 | 11:108098036 | TTATTCAGAGAAAGC[A/G]TTTTTTGTGTTGTTT | 8065 |
rs74634300 | snp | C/T | 0.196771 | 0.244268 | intron-variant | CUL5 | GRCh38.p7 | 11:108083401 | TTTGTGAATCTTTAT[C/T]TACAAGATAGAGTCC | 8065 |
rs74637708 | snp | C/T | 0.0383715 | 0.133092 | intron-variant | CUL5 | GRCh38.p7 | 11:108075634 | TTGAACTCCTGGGCT[C/T]AAGCAATCCTCCCGC | 8065 |
rs74707154 | snp | A/T | 0.16618 | 0.23553 | intron-variant | CUL5 | GRCh38.p7 | 11:108014902 | ATTATTATTATTATT[A/T]TTATTTTTATTTTTG | 8065 |
rs74716522 | snp | C/T | 0.197082 | 0.244335 | intron-variant | CUL5 | GRCh38.p7 | 11:108080290 | GATGAGGTCTTGCTG[C/T]GTTGCTCAGGCTGGT | 8065 |
rs74735899 | snp | G/T | 0.0460142 | 0.144533 | intron-variant | CUL5 | GRCh38.p7 | 11:108016596 | GTCCTGGTGAACCCA[G/T]TTGTCAGTAAGAGCC | 8065 |
rs74861518 | snp | C/T | 0.5 | 0 | intron-variant | CUL5 | GRCh38.p7 | 11:108060481 | TGAAAATCAGAAATG[C/T]TTTTTTTTTTAAACG | 8065 |
rs74879714 | snp | A/G | 0.0014947 | 0.0272969 | intron-variant | CUL5 | GRCh38.p7 | 11:108009375 | TAATCTGTTAAAGGT[A/G]AGACCCTCACTCCAG | 8065 |
rs74914430 | snp | C/T | 0.0524604 | 0.153226 | intron-variant | CUL5 | GRCh38.p7 | 11:108100191 | TTGCCCTGCCAAATA[C/T]GAAAATATTTTAAAA | 8065 |
rs74958279 | snp | A/G | 0.5 | 0 | synonymous-codon | CUL5 | GRCh38.p7 | 11:108095556 | GAATGAAGTTGGTCA[A/G]TATGATTTGGAGGTA | 8065 |
rs75009813 | snp | A/T | 0.00676609 | 0.0577691 | intron-variant | CUL5 | GRCh38.p7 | 11:108039712 | TATAAATGGAATCGT[A/T]TAGTATTTGTCGTTT | 8065 |
rs75176020 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | CUL5 | GRCh38.p7 | 11:108024626 | TTAATAGAAGATACA[A/C]ATGCTGAACTAAAAT | 8065 |
rs75277813 | snp | A/G | 0 | 0 | intron-variant | CUL5 | GRCh38.p7 | 11:108067434 | TTATATTGTGGCTTA[A/G]AATATACTGTTTATT | 8065 |
rs75396671 | snp | C/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108099233 | TGGTCTCGAACTCCT[C/G]GGCTCAAGCAATATG | 8065 |
rs75419400 | snp | G/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108035659 | GTGGGAGGATTGCTT[G/T]AGCCCTCAAGCAGAT | 8065 |
rs75453765 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | CUL5 | GRCh38.p7 | 11:108077032 | GGAGCTGGAAAAATA[C/T]GTTTGGCAGCTTCAG | 8065 |
rs75467498 | snp | A/C | | | intron-variant | CUL5 | GRCh38.p7 | 11:108027026 | TTATTTTTTCACTTC[A/C]TCTCACCCTATCAAT | 8065 |
rs75500101 | snp | C/T | 0.168135 | 0.236216 | intron-variant | CUL5 | GRCh38.p7 | 11:108097009 | TACTACTCCATAGAC[C/T]TCTTAAAAGTTCCAG | 8065 |
rs75582793 | snp | C/T | 0.0165278 | 0.0893908 | upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108007135 | GCTACTTTGCACAGG[C/T]TGGTCTCGAACCCCT | 8065 |
rs75607759 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | CUL5 | GRCh38.p7 | 11:108081812 | GCTTAGTTCAGTTCT[A/G]TTGGTTTATATATTT | 8065 |
rs75677895 | snp | A/G | 0.0295035 | 0.117819 | intron-variant | CUL5 | GRCh38.p7 | 11:108011597 | AGAAGCCAATGTCAT[A/G]AAAAAAACCACCAGC | 8065 |
rs75686791 | snp | A/G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, synonymous-codon, missense | CUL5 | GRCh38.p7 | 11:108106233 | TTGGCGTATTTGCTT[A/G/T]TCCCAATACAAGAAT | 8065 |
rs75694205 | snp | C/T | 0.5 | 0 | intron-variant | CUL5 | GRCh38.p7 | 11:108082648 | AACTGATTTTTTTTT[C/T]TGTTTCTTTTTTTTC | 8065 |
rs75719579 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | CUL5 | GRCh38.p7 | 11:108069523 | TTTTAACTACCCTAG[A/G]AAAAAGTAGTTTCTA | 8065 |
rs75750062 | snp | G/T | 0.5 | 0 | upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108007775 | TTTGTTTTTTTTGTT[G/T]TTTTTTTGAGACAAG | 8065 |
rs75805745 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | CUL5 | GRCh38.p7 | 11:108046580 | AAGAGAGTACATATT[A/G]TATTTAATTAAAAGA | 8065 |
rs75841963 | snp | C/T | 0.0543475 | 0.155628 | intron-variant | CUL5 | GRCh38.p7 | 11:108080253 | AAGCACACACCACCA[C/T]ACTTTACTAATTTCT | 8065 |
rs75856169 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | CUL5 | GRCh38.p7 | 11:108062906 | GCTGGAGTGCTGTGG[C/G]GGGATCTCAGCTCAC | 8065 |
rs75881984 | snp | G/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108022095 | AGTGATCCTCCCACC[G/T]TGCTGGAATTATAGG | 8065 |
rs75971475 | snp | C/T | 0.5 | 0 | intron-variant | CUL5 | GRCh38.p7 | 11:108039016 | TCTGTCCTTCACTCT[C/T]TTTTTTTTTTCTTTT | 8065 |
rs76021043 | snp | C/T | 0.5 | 0 | intron-variant | CUL5 | GRCh38.p7 | 11:108082662 | TCTGTTTCTTTTTTT[C/T]CAGACAGGGTTTCAC | 8065 |
rs76025473 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | CUL5 | GRCh38.p7 | 11:108030939 | TCAGATGATTTTCAC[A/G]TAGGTTGTTGTCAGA | 8065 |
rs76058861 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108022567 | ATGTAACATCTTATA[C/T]TTCTGGCTGATAACA | 8065 |
rs76078002 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | CUL5 | GRCh38.p7 | 11:108035300 | CAGATACATAAGACC[A/C]ATCAGCAGCTTGATT | 8065 |
rs76082777 | snp | G/T | 0 | 0 | upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108007778 | GTTTTTTTTGTTTTT[G/T]TTTTGAGACAAGAGT | 8065 |
rs76185198 | snp | G/T | 0.167809 | 0.236103 | intron-variant | CUL5 | GRCh38.p7 | 11:108075249 | AGGGACGATAGCGTG[G/T]CGTATTAGTAAGTCA | 8065 |
rs76221065 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108012541 | TTTTTTTTTTTTTTT[C/T]AGTTTCCCTTTTTTC | 8065 |
rs76275991 | snp | C/T | 0.5 | 0 | intron-variant | CUL5 | GRCh38.p7 | 11:108039026 | ACTCTTTTTTTTTTT[C/T]CTTTTTAAATTGAGA | 8065 |
rs76294341 | snp | C/T | 0.0165278 | 0.0893908 | intron-variant | CUL5 | GRCh38.p7 | 11:108042131 | CCAATTTTTTTCTTA[C/T]CACTTCACATTTTCA | 8065 |
rs76318001 | snp | G/T | 0 | 0 | intron-variant | CUL5 | GRCh38.p7 | 11:108031784 | TAAATGCCCATCAGT[G/T]ATAGACTGGATAAAG | 8065 |
rs76343995 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | CUL5 | GRCh38.p7 | 11:108015321 | TAGAGGGAACAGCCA[A/G]TGTGAAAGCACAGAG | 8065 |
rs76420504 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | CUL5 | GRCh38.p7 | 11:108081751 | TGCGAGTCTCCGTCT[C/G]AAGAAAAAAATCAGT | 8065 |
rs76448890 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | CUL5 | GRCh38.p7 | 11:108084529 | GATGGACTGATTCCC[G/T]TTCATAGCAAAGGAT | 8065 |
rs76449018 | snp | G/T | 0.0509478 | 0.151255 | intron-variant | CUL5 | GRCh38.p7 | 11:108099726 | AGTCATCTTCCCATG[G/T]TTCCAGGCAGGCTCT | 8065 |
rs76466935 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | CUL5 | GRCh38.p7 | 11:108015392 | GATTTGAATATCATC[A/G]GTGAATGTGGTTAAG | 8065 |
rs76564298 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | CUL5 | GRCh38.p7 | 11:108087181 | TTCTCAGGGCAAAGA[C/T]ATACATTTATACAAA | 8065 |
rs76638109 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | CUL5 | GRCh38.p7 | 11:108030716 | TAACTTTTAGGATGA[A/G]CTATGTTCGTGAATA | 8065 |
rs76651156 | snp | A/G | 0.0832709 | 0.186283 | intron-variant | CUL5 | GRCh38.p7 | 11:108099576 | TTGAGCTCTTTTTTT[A/G]TTGCTAAAATTTTTA | 8065 |
rs76766046 | snp | A/T | 0.5 | 0 | intron-variant | CUL5 | GRCh38.p7 | 11:108079413 | ACCCAGTCCCAAGCA[A/T]TTTTTTTAATGAAAA | 8065 |
rs76771702 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | CUL5 | GRCh38.p7 | 11:108039838 | ATGGATCTGATGTTA[C/T]TGTTTCTTCATTTTC | 8065 |
rs76807653 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | CUL5 | GRCh38.p7 | 11:108093200 | TTGAATAGCTTTTGC[C/T]TTCTTGTGTAACTTG | 8065 |
rs76886532 | snp | A/C | 0.0217236 | 0.101931 | intron-variant | CUL5 | GRCh38.p7 | 11:108040125 | CTCTCCTATTTCCCA[A/C]CTCCTAGATTTTTCT | 8065 |
rs76890945 | snp | A/C | 0.5 | 0 | intron-variant | CUL5 | GRCh38.p7 | 11:108026293 | TTGCACCTTAAATCC[A/C]TGACCACAATGAGGC | 8065 |
rs76973844 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | CUL5 | GRCh38.p7 | 11:108103699 | AATGTGAATGGCATG[A/G]GAAAAAAGGAATTGA | 8065 |
rs77030102 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | CUL5 | GRCh38.p7 | 11:108046443 | TTATTATTTTGAAAG[C/T]AGAACTTCTTGAAGT | 8065 |
rs77040041 | snp | G/T | 0.5 | 0 | intron-variant | CUL5 | GRCh38.p7 | 11:108059660 | GAGATGGGTGGATCA[G/T]GAGGTCAGGAGTTCA | 8065 |
rs77136888 | snp | A/C/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108085646 | TACATGCTGTGACAC[A/C/G]TGGATGAATCTTGAA | 8065 |
rs77140412 | snp | C/T | 0.0337553 | 0.125452 | intron-variant | CUL5 | GRCh38.p7 | 11:108041978 | TAATACATGTTACTT[C/T]TGTTATAGTAAACTA | 8065 |
rs77156257 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | CUL5 | GRCh38.p7 | 11:108026039 | TGTTATTCTGTCATG[A/G]TGGGAAGCAGAAGTC | 8065 |
rs77214373 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | CUL5 | GRCh38.p7 | 11:108047827 | TGATAAAGATAAATT[A/G]TGTTTATTTCAGATA | 8065 |
rs77231599 | snp | C/T | 0.0134861 | 0.0810011 | upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108008152 | GCCATCCTTAACATT[C/T]GGCTACCTTATTAGG | 8065 |
rs77322682 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | CUL5 | GRCh38.p7 | 11:108066653 | ATTCCCGTGGTAACT[A/G]TTGTTTCTACCACTA | 8065 |
rs77346989 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | CUL5 | GRCh38.p7 | 11:108083165 | TGAATTCAGGCATCC[C/T]TGTCTTATTCCTGAT | 8065 |
rs77380939 | snp | G/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108099229 | AGGCTGGTCTCGAAC[G/T]CCTGGGCTCAAGCAA | 8065 |
rs77399013 | snp | A/T | | | utr-variant-3-prime, stop-gained | CUL5 | GRCh38.p7 | 11:108106232 | ATTGGCGTATTTGCT[A/T]GTCCCAATACAAGAA | 8065 |
rs77535217 | snp | C/T | 0.5 | 0 | intron-variant | CUL5 | GRCh38.p7 | 11:108055638 | ATATATATACTTTAT[C/T]TTTTTTTTTTGAGAC | 8065 |
rs77539923 | snp | A/G | 0.0232847 | 0.105357 | intron-variant | CUL5 | GRCh38.p7 | 11:108085334 | CAGACACATAAGGAC[A/G]AATTTTGCATGAATA | 8065 |
rs77541847 | snp | G/T | 0.0193772 | 0.0965046 | intron-variant | CUL5 | GRCh38.p7 | 11:108030765 | GTATGATGTTAATTT[G/T]TGGTTCTTAACCTAG | 8065 |
rs77591987 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | CUL5 | GRCh38.p7 | 11:108095187 | ATACTGCCGTTGTCT[A/G]CAGAATTCAACATGA | 8065 |
rs77620518 | snp | C/G/T | 0.00279162 | 0.0372561 | intron-variant | CUL5 | GRCh38.p7 | 11:108039014 | CTTCTGTCCTTCACT[C/G/T]TTTTTTTTTTTTCTT | 8065 |
rs77644325 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | CUL5 | GRCh38.p7 | 11:108053449 | CTTTTCTTCATGGCC[C/T]CCATATTCTTTTAGT | 8065 |
rs77668062 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | CUL5 | GRCh38.p7 | 11:108073618 | ACCTAGCAACTGTTA[C/T]TTTTCATCAGTGGAG | 8065 |
rs77669929 | snp | A/G | 0.0018608 | 0.0304457 | intron-variant | CUL5 | GRCh38.p7 | 11:108054814 | TAGAACTTAGTATAT[A/G]TGATAATTTGAGCAA | 8065 |
rs77684359 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant, upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108032258 | ACTGCTATAACCTCA[A/G]CATTTTGGGAGACTC | 8065 |
rs77774903 | snp | G/T | 0.0142736 | 0.0832652 | intron-variant, upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108032801 | ACGCTTTTCTCAGCA[G/T]TTCAGTGTCAGGGTT | 8065 |
rs77918129 | snp | A/G | 0.000793467 | 0.0199024 | synonymous-codon, intron-variant, utr-variant-5-prime | CUL5 | GRCh38.p7 | 11:108050039 | CAGCAATAAAAAATC[A/G]AATGTGGAAGACAGT | 8065 |
rs77978059 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | CUL5 | GRCh38.p7 | 11:108087505 | GCATGAAAATACAAT[A/G]TACTGCTGGGTGCAG | 8065 |
rs77992437 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | CUL5 | GRCh38.p7 | 11:108041131 | ACCTTTCTTAGAACT[C/G]TGCTGATTCTTACTG | 8065 |
rs78016975 | snp | A/C | | | intron-variant | CUL5 | GRCh38.p7 | 11:108087010 | ACTGGTAGATGTTAG[A/C]CATTCTTTAAAGATG | 8065 |
rs78051861 | snp | A/C | | | intron-variant | CUL5 | GRCh38.p7 | 11:108015412 | ATGTGGTTAAGGTGC[A/C]TAACCAGAGAATTCT | 8065 |
rs78114924 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108060805 | CCATTGCACTCCAGC[C/T]TGGGCAACGAGTGAA | 8065 |
rs78352448 | snp | A/T | 0.167158 | 0.235875 | intron-variant | CUL5 | GRCh38.p7 | 11:108015668 | TGGGAGAGGGAATAG[A/T]GGACTAATCAGTAAC | 8065 |
rs78374013 | snp | C/T | 5.13941e-05 | 0.00506896 | intron-variant | CUL5 | GRCh38.p7 | 11:108050093 | TTTCTCCTTGTTTTC[C/T]TAATATTCTTCAGAA | 8065 |
rs78379615 | snp | A/C | | | intron-variant | CUL5 | GRCh38.p7 | 11:108022566 | TATGTAACATCTTAT[A/C]TTTCTGGCTGATAAC | 8065 |
rs78433301 | snp | A/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108070624 | TAAGATTTCTAAAGG[A/T]TTTTTTTATTACTTC | 8065 |
rs78444340 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | CUL5 | GRCh38.p7 | 11:108062367 | CAAACTGACTTTCAG[A/G]AATGTAGTCCCATCA | 8065 |
rs78500928 | snp | C/T | 0 | 0 | intron-variant | CUL5 | GRCh38.p7 | 11:108055639 | TATATATACTTTATC[C/T]TTTTTTTTTGAGACA | 8065 |
rs78583857 | snp | C/G | 0.00795532 | 0.062565 | intron-variant | CUL5 | GRCh38.p7 | 11:108087403 | CTTGAATTTTATAAG[C/G]ACAAGAAATTTCAAA | 8065 |
rs78649925 | snp | A/C/G | 0.0449776 | 0.143599 | intron-variant | CUL5 | GRCh38.p7 | 11:108085427 | CAGGGGATGGGGAAG[A/C/G]GGGGGATGGGAAGTT | 8065 |
rs78731801 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | CUL5 | GRCh38.p7 | 11:108059291 | TTATATACCCACAGT[A/G]TGTCAGGCATTATGC | 8065 |
rs78891752 | snp | C/T | 0.16911 | 0.236552 | utr-variant-3-prime | CUL5 | GRCh38.p7 | 11:108106332 | TTGTTCTCAGAACTT[C/T]TTTGGAACTTCTAAT | 8065 |
rs78905861 | snp | C/G | 0.0193772 | 0.0965046 | intron-variant | CUL5 | GRCh38.p7 | 11:108066797 | TTATAGTATAGTAAT[C/G]ATGCATTTTCCAGTT | 8065 |
rs78943189 | snp | C/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108087011 | CTGGTAGATGTTAGC[C/G]ATTCTTTAAAGATGG | 8065 |
rs78996731 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108056608 | GGCTACATTCAGAAG[A/G]CCGGGAAGGCTGTTG | 8065 |
rs79067967 | in-del | -/TTCA | 0.0244538 | 0.107838 | intron-variant | CUL5 | GRCh38.p7 | 11:108079871 | TTGTGTAAAGCTTCT[-/TTCA]TTCTGCATTGTGTTT | 8065 |
rs79093532 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | CUL5 | GRCh38.p7 | 11:108026088 | GAAGTCCATTTTCTC[C/T]GCCTTACCCAACATA | 8065 |
rs79102142 | snp | C/T | 0.00171227 | 0.0292097 | synonymous-codon | CUL5 | GRCh38.p7 | 11:108095634 | AGAGAAAATCAGCTT[C/T]GAAAATCTTAAGCTT | 8065 |
rs79121464 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | CUL5 | GRCh38.p7 | 11:108101173 | GTAATGCTCAGACTT[C/T]ATTTCCTCCTGATCC | 8065 |
rs79248078 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | CUL5 | GRCh38.p7 | 11:108061687 | TTCCTATATTTAAAA[A/G]TAAATTTATGATGTT | 8065 |
rs79260757 | snp | A/T | 0.5 | 0 | intron-variant | CUL5 | GRCh38.p7 | 11:108095114 | TGAGCAGAAATAGTG[A/T]ATTTTTTTCATGAAG | 8065 |
rs79288715 | snp | A/C | 0.0869089 | 0.189476 | intron-variant | CUL5 | GRCh38.p7 | 11:108075728 | TTTTTCTATAGAGAC[A/C]ACATCTAGCTATGTT | 8065 |
rs79408671 | snp | A/C | 0.5 | 0 | intron-variant | CUL5 | GRCh38.p7 | 11:108060829 | GAGTGAAACTGTCTC[A/C]AAAAAAAAAAGAATA | 8065 |
rs79449809 | snp | A/T | 0.5 | 0 | intron-variant | CUL5 | GRCh38.p7 | 11:108027274 | ACCATGCCCAGCTAA[A/T]TTTTTTTTTTTTTCT | 8065 |
rs79456651 | snp | A/C | | | intron-variant | CUL5 | GRCh38.p7 | 11:108020039 | CACCACCCTGCCCCC[A/C]CCCCCACTGGCATTC | 8065 |
rs79466002 | snp | C/T | 0.5 | 0 | intron-variant | CUL5 | GRCh38.p7 | 11:108082647 | CAACTGATTTTTTTT[C/T]CTGTTTCTTTTTTTT | 8065 |
rs79489674 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | CUL5 | GRCh38.p7 | 11:108087194 | GACATACATTTATAC[A/G]AATAAAAGAAATTAT | 8065 |
rs79502322 | snp | G/T | 0 | 0 | upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108007756 | TTTTTGTTTGTAGTT[G/T]TTTTTTGTTTTTTTT | 8065 |
rs79502662 | snp | A/T | 0.0244538 | 0.107838 | intron-variant | CUL5 | GRCh38.p7 | 11:108050991 | AATGGGACCGTAGAT[A/T]TGAAAAGTAAAAAAT | 8065 |
rs79515318 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | CUL5 | GRCh38.p7 | 11:108052593 | ATTTCCTTTTTTGGT[A/G]TTTGTACATGATACT | 8065 |
rs79559256 | snp | C/G | 0.0193772 | 0.0965046 | intron-variant | CUL5 | GRCh38.p7 | 11:108029389 | GAGAGAATTGTAGAC[C/G]TACTAGCAACTGTTG | 8065 |
rs79700611 | snp | C/T | 0.5 | 0 | intron-variant | CUL5 | GRCh38.p7 | 11:108060482 | GAAAATCAGAAATGC[C/T]TTTTTTTTTAAACGA | 8065 |
rs79713500 | snp | A/G | 0.00438332 | 0.0466095 | upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108007306 | CCCTACCACAATATA[A/G]AACATTACATCACCC | 8065 |
rs79734123 | snp | C/T | 0.5 | 0 | intron-variant | CUL5 | GRCh38.p7 | 11:108082646 | ACAACTGATTTTTTT[C/T]TCTGTTTCTTTTTTT | 8065 |
rs79842589 | snp | A/C | 0.0236746 | 0.106192 | intron-variant | CUL5 | GRCh38.p7 | 11:108061434 | TTTTAATATATAGAA[A/C]TCTATACCATAATTG | 8065 |
rs79859524 | in-del | -/TTTTTTTTTTTTTTTTTTTTTTTTTG | | | intron-variant | CUL5 | GRCh38.p7 | 11:108048660 | CACCTTTTTTTTTTT[-/TTTTTTTTTTTTTTTTTTTTTTTTTG]AGGTGGATTCTCACT | 8065 |
rs79931724 | snp | A/C | 0.5 | 0 | intron-variant | CUL5 | GRCh38.p7 | 11:108035752 | AGCAAGACCTTGTCT[A/C]AAAAAAAAAAAAAAA | 8065 |
rs79975835 | snp | G/T | 0.5 | 0 | intron-variant | CUL5 | GRCh38.p7 | 11:108103943 | AGGTGTTTCTCCTAA[G/T]GCTTATCCCTCCCCT | 8065 |
rs80019658 | snp | C/T | 0.198324 | 0.244601 | intron-variant | CUL5 | GRCh38.p7 | 11:108043157 | AGCTCATTGTAACCC[C/T]GAACTTCTGAGTTCA | 8065 |
rs80040779 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | CUL5 | GRCh38.p7 | 11:108101053 | GTTGAAATGTATAAG[C/T]GGGTGTAGTCGTACG | 8065 |
rs80110175 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | CUL5 | GRCh38.p7 | 11:108019930 | TGTGTAGAGATCACA[C/T]GGCAAGAAAGGAAGC | 8065 |
rs80149923 | snp | A/C | 0.5 | 0 | intron-variant | CUL5 | GRCh38.p7 | 11:108044508 | GTGAGACAGTGTCTC[A/C]AAAAAAAAAAAATTA | 8065 |
rs80215910 | snp | C/G | 0.5 | 0 | intron-variant | CUL5 | GRCh38.p7 | 11:108058849 | TAAGCTTGATTATCA[C/G]TCGCTGGGCCTATAG | 8065 |
rs80269031 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | CUL5 | GRCh38.p7 | 11:108054289 | TTGTGCTTTTCTGCT[C/T]CTGAATATTTACTTA | 8065 |
rs80322768 | snp | A/C | 0.0547245 | 0.156101 | intron-variant | CUL5 | GRCh38.p7 | 11:108033972 | GTGATGTCTTTCCAT[A/C]CCCAAATGGAATGTG | 8065 |
rs80341851 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | CUL5 | GRCh38.p7 | 11:108011473 | CACAAGAATTTAAAA[A/G]GTGTTTTAACTTGAA | 8065 |
rs111256202 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108018656 | CTCCAGCCTGGGTGA[C/T]GGAGTGAGACTGTGT | 8065 |
rs111296569 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | CUL5 | GRCh38.p7 | 11:108020662 | GCTAGGATTAGAGGC[A/G]TGAGCCACTGTGCCT | 8065 |
rs111298177 | snp | C/T | 0.5 | 0 | intron-variant | CUL5 | GRCh38.p7 | 11:108084819 | AGGACAGATATAACA[C/T]GTGTTGGTAAGGATA | 8065 |
rs111300588 | snp | A/T | 0.166506 | 0.235645 | intron-variant | CUL5 | GRCh38.p7 | 11:108012653 | CAGGCTGGAGTGCAG[A/T]GGTGTGGATCTCCAC | 8065 |
rs111322949 | snp | C/T | 0 | 0 | intron-variant, upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108032905 | GATTTCCAATATACT[C/T]TTTGTGAGTTTAGGA | 8065 |
rs111333877 | snp | C/T | 0.5 | 0 | intron-variant | CUL5 | GRCh38.p7 | 11:108017344 | GCAGTGAATTGAGAT[C/T]GCACCACTGCACTCC | 8065 |
rs111339569 | snp | C/T | 0.00840818 | 0.0642915 | synonymous-codon | CUL5 | GRCh38.p7 | 11:108072397 | CCAATGTTGAAAGAC[C/T]TGGAGGAACATATCA | 8065 |
rs111441536 | snp | G/T | 0.5 | 0 | intron-variant | CUL5 | GRCh38.p7 | 11:108016248 | TTCTCTTCTCTTCTC[G/T]TCTCGTCTTCTCTTC | 8065 |
rs111485489 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108089011 | AGTCCAAGATAGATA[A/G]CAAGGGATGAATGAG | 8065 |
rs111494631 | snp | A/G | 0.200492 | 0.245049 | intron-variant | CUL5 | GRCh38.p7 | 11:108096781 | ATGTTGGTCAGGCTA[A/G]TCTCAAACTCCTGAC | 8065 |
rs111506857 | snp | A/G | 0.5 | 0 | intron-variant | CUL5 | GRCh38.p7 | 11:108088432 | TCACTAGATTATTTA[A/G]CATGAGAAATTCGCT | 8065 |
rs111510920 | snp | A/C | 0.444444 | 0.157135 | intron-variant | CUL5 | GRCh38.p7 | 11:108022587 | GGCTGATAACACTTA[A/C]CCCCAGCCCAAACAC | 8065 |
rs111524956 | snp | C/T | 0.444444 | 0.157135 | intron-variant | CUL5 | GRCh38.p7 | 11:108050535 | CCACACCCGGCTATT[C/T]TATTGTATTTTTAGT | 8065 |
rs111529442 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108100323 | CGAGGTGGGCAGATT[A/G]CCTGAGGTCAGGAGT | 8065 |
rs111554408 | in-del | -/A/AAAAA | 0.00398564 | 0.0444627 | intron-variant | CUL5 | GRCh38.p7 | 11:108044507 | GTGAGACAGTGTCTC[-/A/AAAAA]AAAAAAAAAAAAATT | 8065 |
rs111559025 | snp | A/G | 0.5 | 0 | intron-variant | CUL5 | GRCh38.p7 | 11:108071815 | CACCTTGGCCTCCCA[A/G]AGTGCTGGAGTTACA | 8065 |
rs111587264 | snp | C/T | 0.168135 | 0.236216 | intron-variant | CUL5 | GRCh38.p7 | 11:108068004 | CACGATCTCGGCTCA[C/T]TGCAATCTCTGCCTC | 8065 |
rs111633544 | snp | A/G | 0.444444 | 0.157135 | intron-variant | CUL5 | GRCh38.p7 | 11:108087961 | CAAGAGCAAAACTCC[A/G]TCTCAAAAAAACTAA | 8065 |
rs111653796 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108048669 | TTTTTTTTTTTTTTT[C/T]TTTTTTTTTTTTTTT | 8065 |
rs111697287 | snp | C/T | 0.5 | 0 | intron-variant | CUL5 | GRCh38.p7 | 11:108073515 | ATATATTCCTATATA[C/T]ATAAAAAACACTTTT | 8065 |
rs111701089 | snp | G/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108038229 | TTTGTTGTTAATGTT[G/T]TTTTTGCCAGTCTGT | 8065 |
rs111701388 | snp | A/G | 0.5 | 0 | intron-variant | CUL5 | GRCh38.p7 | 11:108097144 | CACCTGAGCCCCCCA[A/G]GTAGCTGGGACTACA | 8065 |
rs111705960 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CUL5 | GRCh38.p7 | 11:108026401 | CTAACATTTCCTCCC[C/T]GATCTTCTCAGACAT | 8065 |
rs111730771 | snp | A/T | 0.0138799 | 0.0821421 | intron-variant | CUL5 | GRCh38.p7 | 11:108025024 | CTTATATCTGTGGTT[A/T]ATAGTTTTTATCAAA | 8065 |
rs111742311 | snp | A/G | 0.197393 | 0.244402 | intron-variant | CUL5 | GRCh38.p7 | 11:108027524 | TCATCCACCCACCCC[A/G]GCCTCCCAAAGTGCT | 8065 |
rs111749406 | snp | A/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108063661 | TAATAAAATTTAAAA[A/T]AAATAAATAAATAGT | 8065 |
rs111825673 | snp | G/T | 0.5 | 0 | intron-variant | CUL5 | GRCh38.p7 | 11:108057267 | TCCTGGGCTCGAGCA[G/T]TTCTCCCACCTCGAC | 8065 |
rs111881191 | snp | C/T | 0.5 | 0 | intron-variant | CUL5 | GRCh38.p7 | 11:108102971 | TGGCTAATTTTTGTA[C/T]TTTTTATAGAGATGG | 8065 |
rs111925498 | snp | A/G | 0.5 | 0 | intron-variant | CUL5 | GRCh38.p7 | 11:108095088 | TTTTGCCTCTCTCAC[A/G]TGTAAAAGTTTGAGC | 8065 |
rs112092484 | snp | C/T | 0.199254 | 0.244796 | intron-variant | CUL5 | GRCh38.p7 | 11:108073183 | CTCCAGCCTGGGCGA[C/T]AGATCGAGACTCCGT | 8065 |
rs112094719 | snp | A/G | 0.198634 | 0.244666 | intron-variant | CUL5 | GRCh38.p7 | 11:108053705 | TTTTTTAAGAGATGG[A/G]GTTTTGCTCTGTTGC | 8065 |
rs112115165 | snp | G/T | 0.5 | 0 | intron-variant | CUL5 | GRCh38.p7 | 11:108017694 | ATCTCTACAAAAAAT[G/T]TAATAATTATCCAGG | 8065 |
rs112119967 | snp | A/G | 0.5 | 0 | missense, utr-variant-5-prime | CUL5 | GRCh38.p7 | 11:108033872 | TGAAGCTTTTACGCC[A/G]GGAATCTGTTACAAA | 8065 |
rs112176671 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | CUL5 | GRCh38.p7 | 11:108045379 | GGAGAATTGCTTGAG[A/G]ATTTGAGTTCAAGCC | 8065 |
rs112211266 | snp | A/T | 0.5 | 0 | intron-variant | CUL5 | GRCh38.p7 | 11:108077107 | AAGTAATGATTGGAG[A/T]TAGAAAAGAGGACAG | 8065 |
rs112215681 | snp | C/T | 0.5 | 0 | intron-variant | CUL5 | GRCh38.p7 | 11:108031196 | AACATGGCGAAACCC[C/T]GTCTCTACTGAAAAT | 8065 |
rs112229254 | in-del | -/G | 0.0130921 | 0.0798413 | intron-variant | CUL5 | GRCh38.p7 | 11:108078733 | CAATAAAGGTTAGTT[-/G]AAAAAAAGTCTTTTG | 8065 |
rs112320861 | snp | A/T | 0.0329836 | 0.124112 | intron-variant | CUL5 | GRCh38.p7 | 11:108046607 | AAGATGCTATAGCGA[A/T]TTCAGTTTTTTATAT | 8065 |
rs112356991 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | CUL5 | GRCh38.p7 | 11:108026613 | TTAAATTCACTAGCA[A/G]TTTCTCTCCCTTTCC | 8065 |
rs112396795 | snp | A/G | 0.5 | 0 | intron-variant | CUL5 | GRCh38.p7 | 11:108057597 | ATTGATAGCCTACAA[A/G]ATGACTAATATTCTT | 8065 |
rs112398721 | snp | C/T | 0.444444 | 0.157135 | intron-variant | CUL5 | GRCh38.p7 | 11:108051769 | ATATGCATATGTCTA[C/T]TTCAAACACACCAAT | 8065 |
rs112404126 | snp | C/G | 0 | 0 | intron-variant | CUL5 | GRCh38.p7 | 11:108082665 | GTTTCTTTTTTTTCA[C/G]ACAGGGTTTCACTCT | 8065 |
rs112419456 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | CUL5 | GRCh38.p7 | 11:108031782 | CCCCAATGCCCATCA[A/G]TGATAGACTGGATAA | 8065 |
rs112427329 | snp | G/T | 0.0150606 | 0.0854603 | intron-variant | CUL5 | GRCh38.p7 | 11:108100306 | CCAGCACTTTGGGAG[G/T]CCGAGGTGGGCAGAT | 8065 |
rs112479040 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108080533 | CCTGAGTAGCTGGGA[C/T]TACAGGTGTGTGCCA | 8065 |
rs112495311 | in-del | -/A | 0.5 | 0 | intron-variant | CUL5 | GRCh38.p7 | 11:108041290 | CTGTTTTTTCTTTTT[-/A]TTTTTTTTTGAGACG | 8065 |
rs112502904 | snp | A/C | 0.0364509 | 0.129988 | intron-variant | CUL5 | GRCh38.p7 | 11:108060626 | GGATCACCTGAGGTC[A/C]GGAGTTCAAGACCAG | 8065 |
rs112509170 | snp | A/G | 0.0379877 | 0.132479 | intron-variant | CUL5 | GRCh38.p7 | 11:108100416 | GCTGTGGTGGCGCAT[A/G]CCTGTAATCCCAGCT | 8065 |
rs112573913 | snp | A/C/T | 0.5 | 0 | intron-variant | CUL5 | GRCh38.p7 | 11:108084489 | CCAGGAGGGACATAT[A/C/T]TTCGATTCAGTGGCT | 8065 |
rs112575935 | snp | C/G/T | 0.5 | 0 | intron-variant | CUL5 | GRCh38.p7 | 11:108072162 | CCAGCTTGGGTGACA[C/G/T]ACTGGGACCCTGTCT | 8065 |
rs112590413 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108068475 | AGAAAATTCTTTATT[C/T]GGAAAATTTTAAGCA | 8065 |
rs112633888 | in-del | -/CTTA | 0.0599851 | 0.162463 | upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108008316 | TCTTAGTCCAGAGCT[-/CTTA]CTTATTTCTACGCAT | 8065 |
rs112657026 | snp | G/T | 0.5 | 0 | intron-variant | CUL5 | GRCh38.p7 | 11:108020545 | TTGTGATTTTTTTTT[G/T]TTTGTTTTTTGTTTA | 8065 |
rs112670832 | snp | G/T | 0.5 | 0 | intron-variant | CUL5 | GRCh38.p7 | 11:108057349 | GTCAAAAGTTTGAAA[G/T]GAAATAGGATATTTG | 8065 |
rs112702952 | snp | C/T | 0.198014 | 0.244535 | intron-variant | CUL5 | GRCh38.p7 | 11:108055719 | CACTGCAACCTCTGC[C/T]TCTCAGGCTCAAGCA | 8065 |
rs112750774 | snp | G/T | 0.5 | 0 | intron-variant | CUL5 | GRCh38.p7 | 11:108043933 | GAGGCTGAGGCAGGA[G/T]AATCATTTGAACCCA | 8065 |
rs112752100 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | CUL5 | GRCh38.p7 | 11:108014850 | GGTACTATGAATAAA[A/G]ACAACCAGGGTAAAA | 8065 |
rs112764455 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | CUL5 | GRCh38.p7 | 11:108056018 | TCCTGGCCTCAAGCA[A/G]TCCTTCTTGCTCAGC | 8065 |
rs112767543 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108064586 | GAGGTGTCAGGTGCC[C/T]GTAATCCCAGCTACT | 8065 |
rs112772019 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108048668 | TTTTTTTTTTTTTTT[C/T]TTTTTTTTTTTTTTT | 8065 |
rs112841454 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | CUL5 | GRCh38.p7 | 11:108075997 | ACTTAGCATGAATCC[A/G]ATATACAGTATAATT | 8065 |
rs112868190 | snp | G/T | 0.5 | 0 | intron-variant | CUL5 | GRCh38.p7 | 11:108022350 | ATTTTTCTATTTTTG[G/T]TTACATTCTTGTGTT | 8065 |
rs112916103 | snp | A/G | 0.5 | 0 | intron-variant | CUL5 | GRCh38.p7 | 11:108048380 | AGATGAATTTGCCTA[A/G]GCTTATTAATGCAGC | 8065 |
rs112948114 | snp | G/T | 0.5 | 0 | intron-variant | CUL5 | GRCh38.p7 | 11:108038804 | TTTTAGCCATATTTT[G/T]GCCATGTTAATCGTT | 8065 |
rs112973741 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CUL5 | GRCh38.p7 | 11:108019596 | CTTGTAACGTAGTAG[C/T]GCAATAACACATCAC | 8065 |
rs113034014 | snp | A/T | 0.5 | 0 | intron-variant | CUL5 | GRCh38.p7 | 11:108037817 | ATGTAAAACATTCTC[A/T]TTAAGGAATGATGGG | 8065 |
rs113038324 | snp | C/G | 0.5 | 0 | intron-variant | CUL5 | GRCh38.p7 | 11:108085138 | TAAATGTTCATAGTA[C/G]AGTGGCATTACTCTT | 8065 |
rs113038994 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108028598 | AATCACAGCACTTTC[A/G]GAGGCCGAAGCGGGC | 8065 |
rs113116875 | snp | A/G | 0.5 | 0 | intron-variant | CUL5 | GRCh38.p7 | 11:108102644 | CTGGTTATCATATCT[A/G]TATAGGGGAAGTTGA | 8065 |
rs113157122 | snp | A/G | 0.5 | 0 | intron-variant | CUL5 | GRCh38.p7 | 11:108098194 | TTTTACAGAGAATGT[A/G]GTCACTTGTTTTATT | 8065 |
rs113199388 | snp | A/G | 0.5 | 0 | intron-variant | CUL5 | GRCh38.p7 | 11:108055513 | GTGGAGTGCAGTGGT[A/G]CAATTATACCTCACT | 8065 |
rs113308636 | snp | C/T | 0.5 | 0 | intron-variant | CUL5 | GRCh38.p7 | 11:108014921 | TTTTTATTTTTGAGA[C/T]GGGGTCTCACTCTCT | 8065 |
rs113312984 | snp | A/G | 0.5 | 0 | intron-variant | CUL5 | GRCh38.p7 | 11:108026415 | CCGATCTTCTCAGAC[A/G]TTGTCGTTATTTCCA | 8065 |
rs113357497 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | CUL5 | GRCh38.p7 | 11:108017660 | TTCAAGACCAGTCTG[A/G]GCAACATAGTAAGAC | 8065 |
rs113370626 | snp | A/C | 0.5 | 0 | intron-variant | CUL5 | GRCh38.p7 | 11:108063195 | CTATTTCTCCCCCAC[A/C]ACCTCACTACCCTAC | 8065 |
rs113406810 | snp | C/T | 0 | 0 | intron-variant | CUL5 | GRCh38.p7 | 11:108081640 | ACCTGTAGTCCCAGC[C/T]ACTCGGGAGGCTGAG | 8065 |
rs113431120 | snp | A/G | 0.5 | 0 | intron-variant | CUL5 | GRCh38.p7 | 11:108052523 | TGCCTCGGCCTCCCA[A/G]ATTGTTGGGACTACA | 8065 |
rs113437428 | snp | C/G | 0.5 | 0 | intron-variant | CUL5 | GRCh38.p7 | 11:108069393 | CTTCTCTTCCACTGT[C/G]TGTTTCTTCTCTACC | 8065 |
rs113538827 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | CUL5 | GRCh38.p7 | 11:108023404 | CTTGGTTTTAAGGTC[A/G]TATGAGTAGTTCAGA | 8065 |
rs113549152 | snp | A/G | 0.5 | 0 | intron-variant | CUL5 | GRCh38.p7 | 11:108017782 | TTGAGCACAGATCAA[A/G]GCTGCAGTGAGCAAT | 8065 |
rs113605419 | in-del | -/A | 0.5 | 0 | intron-variant | CUL5 | GRCh38.p7 | 11:108017846 | GTGAGACCCTGTCTC[-/A]AAAAAAAAAAAGTGT | 8065 |
rs113606327 | snp | C/G | 0.0260105 | 0.111035 | intron-variant | CUL5 | GRCh38.p7 | 11:108010031 | TTAGGGCGCAGGAAA[C/G]TTACCTTGTCAAAGA | 8065 |
rs113615078 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | CUL5 | GRCh38.p7 | 11:108072968 | AGCACTTTGGGAGGC[C/T]GAGGTGGGCAGATCA | 8065 |
rs113622825 | snp | A/G | 0.0368353 | 0.130617 | intron-variant | CUL5 | GRCh38.p7 | 11:108080354 | TCAGCCTCCCAAAGT[A/G]TTGAGCTTACAGGCA | 8065 |
rs113641256 | snp | A/G | 0.5 | 0 | intron-variant | CUL5 | GRCh38.p7 | 11:108022010 | TCTACCTATCTATCC[A/G]TCGATCCATCCATTC | 8065 |
rs113689317 | snp | A/G | 0.200492 | 0.245049 | intron-variant | CUL5 | GRCh38.p7 | 11:108095989 | TAATCCCAGCTACTT[A/G]GGAGGCTGAGGCAGG | 8065 |
rs113698998 | snp | A/G | 0.5 | 0 | intron-variant | CUL5 | GRCh38.p7 | 11:108029385 | GAATGAGAGAATTGT[A/G]GACCTACTAGCAACT | 8065 |
rs113729240 | snp | G/T | 0.5 | 0 | intron-variant | CUL5 | GRCh38.p7 | 11:108053102 | CTAGTTCATTAAAAG[G/T]TTAGGTATTTATGTT | 8065 |
rs113786799 | in-del | -/AGTG | 0.133093 | 0.220981 | intron-variant | CUL5 | GRCh38.p7 | 11:108072534 | AGGATTATTGAAAAT[-/AGTG]AGCGGTTACCAGAGG | 8065 |
rs113791056 | snp | A/G | 0.5 | 0 | intron-variant | CUL5 | GRCh38.p7 | 11:108016150 | CCACTCCTGAGCTCC[A/G]GTGATCTTCCTGCGT | 8065 |
rs113849432 | snp | A/T | 0.0236746 | 0.106192 | intron-variant | CUL5 | GRCh38.p7 | 11:108042425 | CGGGGTTTCACCATG[A/T]TGTCTAGGCTGGTCC | 8065 |
rs113931220 | snp | A/G | 0.167158 | 0.235875 | intron-variant | CUL5 | GRCh38.p7 | 11:108081220 | CAGAATCTGGGAGGT[A/G]GAGGTCGCAGTGAGC | 8065 |
rs113944159 | snp | G/T | 0 | 0 | intron-variant | CUL5 | GRCh38.p7 | 11:108047913 | TGTTCTTAACAGATG[G/T]TAAAAAATATGCTGA | 8065 |
rs114099764 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | CUL5 | GRCh38.p7 | 11:108025517 | ATATCACTCGGGGTA[G/T]GGCTACTTTGGCTCC | 8065 |
rs114142704 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | CUL5 | GRCh38.p7 | 11:108011972 | TAATAATTTTATTGT[C/T]TGTTTAAAGCAAGTG | 8065 |
rs114378212 | snp | C/G | 0.0189856 | 0.0955633 | upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108007143 | GCACAGGCTGGTCTC[C/G]AACCCCTGGGCTCAA | 8065 |
rs114428640 | snp | C/T | 0.00755907 | 0.0610114 | utr-variant-5-prime, upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108008863 | TGCAGCCTCGGGACC[C/T]ACCGAGGCTTCCAGG | 8065 |
rs114432340 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | CUL5 | GRCh38.p7 | 11:108016140 | AGACTGGTCTCCACT[C/T]CTGAGCTCCAGTGAT | 8065 |
rs114440904 | snp | C/G | 0.00993419 | 0.0697739 | intron-variant | CUL5 | GRCh38.p7 | 11:108069965 | TTCAATAATCCTATA[C/G]TTAAGGTAAGTGAAA | 8065 |
rs114467909 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | CUL5 | GRCh38.p7 | 11:108010397 | ATGTCTTCTTTAGAC[C/T]ACTGATATTTGATTG | 8065 |
rs114471866 | snp | A/G | 0.0189856 | 0.0955633 | downstream-variant-500B | CUL5 | GRCh38.p7 | 11:108107873 | GGTAAATTAATCTCA[A/G]CCAGCCTTAGGAATC | 8065 |
rs114478753 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108081917 | GTTTCAAGTTGGTTC[C/T]TTTTCAAGATCATTC | 8065 |
rs114516217 | snp | A/G | 0.021333 | 0.101051 | intron-variant | CUL5 | GRCh38.p7 | 11:108080099 | GACTCTTGATGTTGA[A/G]CAATTTTTCATCTTT | 8065 |
rs114517482 | snp | A/G | 0.0509478 | 0.151255 | intron-variant | CUL5 | GRCh38.p7 | 11:108070554 | TGATGAATCTTTTTA[A/G]AATGTAATAAAACAC | 8065 |
rs114554548 | snp | A/G | 0.029116 | 0.117091 | intron-variant | CUL5 | GRCh38.p7 | 11:108019384 | CAAATAACTAACCTC[A/G]TAATTCACATGAATT | 8065 |
rs114592239 | snp | A/G | 0.0279526 | 0.114869 | intron-variant | CUL5 | GRCh38.p7 | 11:108041578 | ACCATGCCCACACCC[A/G]GCCTGGTTTTTTCTT | 8065 |
rs114718022 | snp | A/G | 0.029116 | 0.117091 | intron-variant | CUL5 | GRCh38.p7 | 11:108058931 | CTTCCGAGCTGTGCT[A/G]CTGAACAGGCATGTT | 8065 |
rs114718209 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | CUL5 | GRCh38.p7 | 11:108062284 | CCTCTTGGAATAGAA[G/T]CTCCTGGAAATTAGA | 8065 |
rs114738457 | snp | C/G/T | 0.0295035 | 0.117819 | intron-variant | CUL5 | GRCh38.p7 | 11:108035112 | CTGTTGTTGCAAACT[C/G/T]TAACCAATCCAGAAA | 8065 |
rs114741365 | snp | G/T | 0.0341408 | 0.126114 | intron-variant | CUL5 | GRCh38.p7 | 11:108064571 | CAAAAATTAGCGGGC[G/T]AGGTGTCAGGTGCCC | 8065 |
rs114744657 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | CUL5 | GRCh38.p7 | 11:108094724 | ATCTTTATAGTCTTA[C/T]TGATTTTTCACCCAA | 8065 |
rs114838522 | snp | A/G | 0.021333 | 0.101051 | utr-variant-3-prime, intron-variant | CUL5 | GRCh38.p7 | 11:108104750 | TTAAAAAATGTACTT[A/G]CACAAGGAAGGATCT | 8065 |
rs114917973 | snp | A/G | 0.0283406 | 0.115616 | intron-variant | CUL5 | GRCh38.p7 | 11:108089110 | CAAACAAGAAAAAAA[A/G]TAAGATATTGGGCAA | 8065 |
rs114960880 | snp | A/C | 0.0193772 | 0.0965046 | intron-variant | CUL5 | GRCh38.p7 | 11:108052503 | ATAGACTCCAGCGAT[A/C]CACCTGCCTCGGCCT | 8065 |
rs115055232 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | CUL5 | GRCh38.p7 | 11:108042712 | AAACCATCTTTTGTT[G/T]ATATGCATAAAATAG | 8065 |
rs115149291 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | CUL5 | GRCh38.p7 | 11:108041108 | AGAATTCTTCAACAG[C/T]CTTACCAACCTTTCT | 8065 |
rs115263889 | snp | A/G | 0.0325976 | 0.123435 | intron-variant | CUL5 | GRCh38.p7 | 11:108076891 | GATAGGGAAGACTGT[A/G]AGAGAAATAGTTTTT | 8065 |
rs115300736 | snp | G/T | 0.0244538 | 0.107838 | intron-variant | CUL5 | GRCh38.p7 | 11:108082308 | TTTTTTTAAGACAGG[G/T]TCCACTGTGTCACCG | 8065 |
rs115311547 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | CUL5 | GRCh38.p7 | 11:108039584 | GTCCATTCCCCAAAC[A/G]CTTCATCATCAGAAA | 8065 |
rs115391635 | snp | C/G | 0.0322114 | 0.122752 | intron-variant | CUL5 | GRCh38.p7 | 11:108081899 | AAAGCAAGATGTGTG[C/G]ATGTTTCAAGTTGGT | 8065 |
rs115454932 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CUL5 | GRCh38.p7 | 11:108088350 | CAGCACTTAGGGGAA[C/T]GTAAAAGTGAGTGCC | 8065 |
rs115461171 | snp | A/T | 0.0185938 | 0.0946107 | upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108008150 | TAGCCATCCTTAACA[A/T]TTGGCTACCTTATTA | 8065 |
rs115477105 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | CUL5 | GRCh38.p7 | 11:108071574 | TTATTTTTTGAGACC[A/G]TCTTGCCCTGTCACC | 8065 |
rs115504928 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CUL5 | GRCh38.p7 | 11:108076899 | AGACTGTAAGAGAAA[C/T]AGTTTTTGGAGAGAT | 8065 |
rs115600167 | snp | C/T | 0.0482946 | 0.147699 | intron-variant | CUL5 | GRCh38.p7 | 11:108022153 | TGCAACATTTGACAT[C/T]ATTAAAATATTGCCA | 8065 |
rs115723216 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | CUL5 | GRCh38.p7 | 11:108083420 | AAGATAGAGTCCCAG[A/G]AGTGAGGATTGCTGG | 8065 |
rs115768369 | snp | A/T | 0.021333 | 0.101051 | intron-variant | CUL5 | GRCh38.p7 | 11:108086076 | TCTAAAACCATATAT[A/T]ATTGGAGTCATAGAG | 8065 |
rs115782802 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | CUL5 | GRCh38.p7 | 11:108075366 | GTTCTTGAAGTTTCC[C/T]GCCTGCCACTTGCAT | 8065 |
rs115818543 | snp | A/G | 0.0543475 | 0.155628 | intron-variant | CUL5 | GRCh38.p7 | 11:108074885 | ATAGACATGGTGGGC[A/G]TGGTGTGAAGTCTTA | 8065 |
rs115826471 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CUL5 | GRCh38.p7 | 11:108098260 | GAGTTTGTTTTAAAG[C/T]AATATGTAGGTTATT | 8065 |
rs115999691 | snp | C/T | 0.0513262 | 0.151752 | intron-variant | CUL5 | GRCh38.p7 | 11:108016495 | CTGGGCTCAAGCAAT[C/T]TGCCCTGTCCTTCCA | 8065 |
rs116018089 | snp | C/G | 0.0329836 | 0.124112 | intron-variant | CUL5 | GRCh38.p7 | 11:108044190 | TCAAATTAATATGGA[C/G]ACAAAACTTTGGGCT | 8065 |
rs116044255 | snp | C/T | 0.0322114 | 0.122752 | intron-variant | CUL5 | GRCh38.p7 | 11:108084735 | ACATAAGGACTTTAA[C/T]TAATTAAGATTAATA | 8065 |
rs116176321 | snp | C/T | 0.0337553 | 0.125452 | intron-variant | CUL5 | GRCh38.p7 | 11:108049689 | ATATTTGGGTTGTTT[C/T]TATTTTTTATCTATT | 8065 |
rs116239445 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | CUL5 | GRCh38.p7 | 11:108076324 | CAGGCATGAGCCACC[A/G]TGCCCAGCCCAGTAT | 8065 |
rs116269741 | snp | C/T | 0.0543475 | 0.155628 | intron-variant | CUL5 | GRCh38.p7 | 11:108091022 | ATTTACTACGAGAAA[C/T]CTTTAGAATTAAATT | 8065 |
rs116358024 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | CUL5 | GRCh38.p7 | 11:108071774 | CCTGACTGGTCTTTT[C/T]AACTCCTGGGCTCAA | 8065 |
rs116378290 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108085341 | ATAAGGACAAATTTT[C/G]CATGAATATGGTTGT | 8065 |
rs116454795 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | CUL5 | GRCh38.p7 | 11:108019584 | TTTATTGTAGCCCTT[A/G]TAACGTAGTAGTGCA | 8065 |
rs116546658 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | CUL5 | GRCh38.p7 | 11:108077101 | TCACCAAAGTAATGA[C/T]TGGAGATAGAAAAGA | 8065 |
rs116638813 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | CUL5 | GRCh38.p7 | 11:108031488 | TGGTATAAGAAAGGG[A/G]TCTGGTTTTACTTTT | 8065 |
rs116648073 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | CUL5 | GRCh38.p7 | 11:108040088 | GCCTCCTTAAGACTT[C/T]TGAGAAGCTTCTATT | 8065 |
rs116651865 | snp | C/T | 0.0322114 | 0.122752 | intron-variant | CUL5 | GRCh38.p7 | 11:108034239 | CCCAGGGGAGTCACA[C/T]AGGACACACTTAATT | 8065 |
rs116652064 | snp | C/T | 0.0341408 | 0.126114 | intron-variant | CUL5 | GRCh38.p7 | 11:108102159 | CCTGAGTAGCTGGGA[C/T]TAGAGGTGCTCGCCA | 8065 |
rs116676385 | snp | A/G | 0.0283406 | 0.115616 | intron-variant | CUL5 | GRCh38.p7 | 11:108077852 | CAGGAGGCCAGCTAA[A/G]ACAGGAGAATCACTT | 8065 |
rs116775342 | snp | A/T | 0.0197687 | 0.0974348 | intron-variant | CUL5 | GRCh38.p7 | 11:108039849 | GTTATTGTTTCTTCA[A/T]TTTCCCTTTGTTTTT | 8065 |
rs116797539 | snp | A/G | 0.0547245 | 0.156101 | intron-variant | CUL5 | GRCh38.p7 | 11:108065447 | TTTAGCTTATAGTGC[A/G]AGGCTTGCTAGAACT | 8065 |
rs116836123 | snp | A/C | 0.0182019 | 0.0936463 | intron-variant | CUL5 | GRCh38.p7 | 11:108053538 | CCACCAGACATTAAA[A/C]TTCACATGCAGAGTT | 8065 |
rs116984953 | snp | A/C | 0.0170251 | 0.090679 | intron-variant | CUL5 | GRCh38.p7 | 11:108031287 | TGAAAATCACCTGAC[A/C]CTGGGAGGTAGAGGC | 8065 |
rs117030500 | snp | C/T | 0.0162398 | 0.0886349 | utr-variant-3-prime | CUL5 | GRCh38.p7 | 11:108106909 | AGAGGCTATCTTAAC[C/T]TCTGAATACCCATCT | 8065 |
rs117064123 | snp | G/T | 0.0346596 | 0.126998 | intron-variant | CUL5 | GRCh38.p7 | 11:108068314 | CTGAAAAAACCTTTT[G/T]TTTTGTTTTGTTTTG | 8065 |
rs117152510 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | CUL5 | GRCh38.p7 | 11:108014582 | ATTTATAATCTGCTT[A/G]TGAGATTGGCCATGG | 8065 |
rs117161975 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | CUL5 | GRCh38.p7 | 11:108017084 | GAGCATTTATGCTGT[A/G]CTGGATACCATTTTA | 8065 |
rs117203985 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108097881 | ATCACTCTAAACTTA[C/G]ATCATTTAGTTGTTT | 8065 |
rs117204054 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | CUL5 | GRCh38.p7 | 11:108010912 | TAATCTTCACAGTGT[A/T]CCTACAATATAGGTG | 8065 |
rs117240059 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CUL5 | GRCh38.p7 | 11:108053489 | TTTAGATTTTCATTA[A/G]CAGTGCTCCTGAAAT | 8065 |
rs117264171 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108049381 | GGGTATTGCTCTGTC[A/G]CCCAGGCCAGAGTGC | 8065 |
rs117267052 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108074876 | TAAGGGAGTATAGAC[A/T]TGGTGGGCGTGGTGT | 8065 |
rs117271626 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108039902 | ATTAGTGGTTGCCTT[C/T]GTGTTTCTTGGTCTT | 8065 |
rs117277112 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108030599 | CTGAGATCGTGCCAC[C/T]GCGCTCCAGCTTGGG | 8065 |
rs117373213 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | CUL5 | GRCh38.p7 | 11:108042848 | GCTCACTGCAACCTC[C/T]GCTTCCAGGGTTCAA | 8065 |
rs117412477 | snp | A/T | 0.0134861 | 0.0810011 | intron-variant | CUL5 | GRCh38.p7 | 11:108066872 | TATGAACCATACACA[A/T]GTTTTTAGGTATATA | 8065 |
rs117439163 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CUL5 | GRCh38.p7 | 11:108024066 | CCTGATGAAATTAAG[C/T]CAAGGGCTGGATCTG | 8065 |
rs117441851 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | CUL5 | GRCh38.p7 | 11:108065446 | CTTTAGCTTATAGTG[C/T]GAGGCTTGCTAGAAC | 8065 |
rs117460699 | snp | C/G/T | 0.00795532 | 0.062565 | intron-variant | CUL5 | GRCh38.p7 | 11:108057930 | AAATAAAGAATATTG[C/G/T]CTGGGTGCAGTGGCT | 8065 |
rs117489632 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | CUL5 | GRCh38.p7 | 11:108017488 | GATGAATACTGACAC[C/T]AAAGACATAAAGAAT | 8065 |
rs117793310 | snp | A/G | 0.0146672 | 0.084371 | intron-variant, upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108032379 | TGGGCATGGTGGTGC[A/G]CACGTGTAGTCCCAG | 8065 |
rs117816999 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | CUL5 | GRCh38.p7 | 11:108100122 | TTTTTATCAGAATAA[A/G]TAAGAATGATTGAGA | 8065 |
rs117886794 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | CUL5 | GRCh38.p7 | 11:108096375 | TTGGTGGCTGTATCC[A/C]CAGCTACTTGGAAGG | 8065 |
rs117953901 | snp | A/G | 0.0023933 | 0.0345097 | upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108007389 | AATTTTGTATTATGT[A/G]CCTGCGCTATTTTTA | 8065 |
rs117989312 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | CUL5 | GRCh38.p7 | 11:108063937 | GCTACTTTAACTGGG[A/G]TGAGATGATGTCTCG | 8065 |
rs118016304 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108085107 | GAAAACATACTTTCA[C/T]TCAGAAACATGCTCA | 8065 |
rs118029055 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108057187 | CAGGTACGTGCCACT[A/G]CACCTGGCTAATTTT | 8065 |
rs118043232 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | CUL5 | GRCh38.p7 | 11:108050405 | GGAGTGTCACTCTGT[C/T]GCCTAGGCTGGAGTG | 8065 |
rs118044691 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | CUL5 | GRCh38.p7 | 11:108040470 | TACAAAAATCGGCTG[A/G]GTGTGGTGTTGTGCA | 8065 |
rs118096972 | snp | A/C | 0.0134861 | 0.0810011 | intron-variant | CUL5 | GRCh38.p7 | 11:108035298 | ATCAGATACATAAGA[A/C]CAATCAGCAGCTTGA | 8065 |
rs137867679 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | CUL5 | GRCh38.p7 | 11:108027698 | AAGCATGAACTATTG[C/T]GCCTGGCTCCTCGTT | 8065 |
rs137925026 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | CUL5 | GRCh38.p7 | 11:108102392 | AGTGCAGTGGTACAA[C/T]CTCAGCTCACTGCAA | 8065 |
rs138005443 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | CUL5 | GRCh38.p7 | 11:108064987 | TGCCAGGCTTTTCTT[C/T]GTTGGGAGAAATTTT | 8065 |
rs138023074 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | CUL5 | GRCh38.p7 | 11:108036179 | TCCATCTGGAGATTT[C/G]GTTTGTTTTCATGTT | 8065 |
rs138083925 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | CUL5 | GRCh38.p7 | 11:108016958 | AGCAAGACCTACCAC[C/G]TCTACAAAAATAAAA | 8065 |
rs138088543 | snp | C/G | 0.0329836 | 0.124112 | intron-variant | CUL5 | GRCh38.p7 | 11:108052251 | TTTGGGATTAGACCA[C/G]ACGCAGTCGACCCTT | 8065 |
rs138135880 | snp | A/G | 0.039522 | 0.134904 | intron-variant | CUL5 | GRCh38.p7 | 11:108030544 | CGGGAAGCTGAGGCA[A/G]GAGAATCGCTTGAAC | 8065 |
rs138143013 | snp | C/T | 1.66846e-05 | 0.00288826 | stop-gained, intron-variant, utr-variant-5-prime | CUL5 | GRCh38.p7 | 11:108050061 | GAAGACAGTATTGTT[C/T]GAAAGGTAAGACTAT | 8065 |
rs138182387 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | CUL5 | GRCh38.p7 | 11:108083639 | TACAAAATGTTTTAA[A/G]AATTAGACGAGCATG | 8065 |
rs138193887 | snp | A/G | 0.0850919 | 0.187897 | intron-variant | CUL5 | GRCh38.p7 | 11:108096623 | TCAGGCTGGAGTGCA[A/G]TGGCGCAATCTCAGC | 8065 |
rs138210443 | snp | A/C | 0.00795532 | 0.062565 | intron-variant | CUL5 | GRCh38.p7 | 11:108050874 | ACCAGTCATGATTTA[A/C]TGGAAAGAACTCAGT | 8065 |
rs138221170 | snp | A/T | 0.000184185 | 0.00959472 | intron-variant | CUL5 | GRCh38.p7 | 11:108094378 | CTCTTCCTTCTTTGG[A/T]TTATATTTATAGGAA | 8065 |
rs138319729 | snp | A/C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108080960 | GATTTATCATTATTT[A/C/T]TTTATTTATTTATTT | 8065 |
rs138322707 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108045612 | TAACACTTTTAATTC[C/T]AGCACTTTGGAGACT | 8065 |
rs138355588 | in-del | -/C | | | intron-variant | CUL5 | GRCh38.p7 | 11:108019225 | GGGTGGGGTGGATCC[-/C]TGGAATCATTTCCCC | 8065 |
rs138398858 | snp | A/G | 0.0236746 | 0.106192 | intron-variant | CUL5 | GRCh38.p7 | 11:108035604 | AAATTATCTGGGTGT[A/G]GTGGCACATGCCTGT | 8065 |
rs138401066 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CUL5 | GRCh38.p7 | 11:108015653 | GGTCATGGGTAGGAA[C/T]GGGAGAGGGAATAGT | 8065 |
rs138455557 | snp | G/T | 0.0217236 | 0.101931 | intron-variant | CUL5 | GRCh38.p7 | 11:108031799 | GATAGACTGGATAAA[G/T]AAAATGTGGTACATA | 8065 |
rs138481922 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | CUL5 | GRCh38.p7 | 11:108088808 | AGTGCAAGACCTCTC[A/G]GGGGGTTATTTTTCT | 8065 |
rs138488259 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | CUL5 | GRCh38.p7 | 11:108010104 | CCACAGGGGCAGATT[C/G]TCCACCAGTTAAAAA | 8065 |
rs138515683 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108064447 | GCTCAGTGGCTCACG[C/T]CTGTAATCCCAGCAC | 8065 |
rs138616958 | in-del | -/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108100106 | GAATTTTACAAATTG[-/T]TTTTTTATCAGAATA | 8065 |
rs138650456 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | CUL5 | GRCh38.p7 | 11:108020588 | GGTCTCACCACGTTG[C/G]CCAGGCTGGTCTCAA | 8065 |
rs138673197 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | CUL5 | GRCh38.p7 | 11:108101133 | CCATAATTATGTACA[A/G]TCCAATAATCTAAGC | 8065 |
rs138765555 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | CUL5 | GRCh38.p7 | 11:108068012 | CGGCTCACTGCAATC[C/T]CTGCCTCCCAGGTTT | 8065 |
rs138788933 | snp | A/C | 0.00755907 | 0.0610114 | intron-variant | CUL5 | GRCh38.p7 | 11:108089281 | TGATATTTAGACCGA[A/C]TAACAATTTGGTTAT | 8065 |
rs138794562 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | CUL5 | GRCh38.p7 | 11:108010302 | AAGGATGAACCACTT[C/T]TTCCTGAGGCCTCTC | 8065 |
rs138795364 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | CUL5 | GRCh38.p7 | 11:108011703 | TGCGATCTTGGTTCA[C/G]TGCAACTTCCGCCTC | 8065 |
rs138797087 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108046827 | ACATTGCTGTTATGT[A/G]TAAATCAAAAATTTT | 8065 |
rs138797563 | snp | A/C | 0.0138799 | 0.0821421 | intron-variant | CUL5 | GRCh38.p7 | 11:108060111 | AAGTTATAAATTATT[A/C]ACATTAAAATAAGCA | 8065 |
rs138873899 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | CUL5 | GRCh38.p7 | 11:108069136 | ATAGTACATCCCTGT[A/G]GTCCTAGCTACTCAA | 8065 |
rs138876250 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | CUL5 | GRCh38.p7 | 11:108040756 | TGCACTCCAGGCAGG[A/G]TGACAGGGAGAGACC | 8065 |
rs138901219 | snp | A/G/T | 0.000231181 | 0.0107489 | missense | CUL5 | GRCh38.p7 | 11:108098419 | AGAAAAAATGCAAAG[A/G/T]TTCAGAAAAGGGGTA | 8065 |
rs138911923 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | CUL5 | GRCh38.p7 | 11:108084445 | ACAGGACTGGAGTAA[C/T]AAAACCCATTGGACA | 8065 |
rs138912773 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | CUL5 | GRCh38.p7 | 11:108056504 | AGTATGTATCCTCTT[G/T]GGTTGAAATAGTTTT | 8065 |
rs138939451 | snp | A/G | 0.000232384 | 0.0107767 | synonymous-codon, utr-variant-5-prime | CUL5 | GRCh38.p7 | 11:108054753 | AACACAAGCACCCTC[A/G]TATTTACAACAAAAT | 8065 |
rs138940798 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108083023 | TCTTTCAGCTTTTCT[C/G]TATATAAGATCATGA | 8065 |
rs139021679 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108050554 | TGTATTTTTAGTGGA[A/G]ACCAGGTTTCACCAT | 8065 |
rs139034555 | in-del | -/TCT | 0.0260105 | 0.111035 | intron-variant | CUL5 | GRCh38.p7 | 11:108079058 | ACATGAGTAGATAGA[-/TCT]TCTTCTCTTTCACCC | 8065 |
rs139080719 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | CUL5 | GRCh38.p7 | 11:108053977 | CAGCCTCCAGAATAG[C/G]TGAGATTACAGGTGT | 8065 |
rs139114486 | snp | C/T | 0.000927797 | 0.0215183 | intron-variant | CUL5 | GRCh38.p7 | 11:108097762 | AGTTTAATGTAAGCT[C/T]GTTAGTTGATCTAAA | 8065 |
rs139143673 | snp | C/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108056180 | TCAGTATAAGGAAAG[C/T]TAGAATCTAGTTGGG | 8065 |
rs139160419 | snp | A/C | | | intron-variant | CUL5 | GRCh38.p7 | 11:108080964 | TATCATTATTTATTT[A/C]TTTATTTATTTATTT | 8065 |
rs139182529 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | CUL5 | GRCh38.p7 | 11:108022259 | CGAACCAGTAGGTCA[A/G]CATTTGTATTATTTT | 8065 |
rs139192571 | snp | A/C | 0.0130921 | 0.0798413 | intron-variant | CUL5 | GRCh38.p7 | 11:108048173 | CTTCAGTTGAACATA[A/C]CTTGTTAGGAAGGAC | 8065 |
rs139205036 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | CUL5 | GRCh38.p7 | 11:108017826 | CACTCTAGCCTGGAC[A/G]ACAGAGTGAGACCCT | 8065 |
rs139234281 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CUL5 | GRCh38.p7 | 11:108037553 | AGTCCAGGAGAAACG[A/G]AATCCAAACTTCCAA | 8065 |
rs139261037 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | CUL5 | GRCh38.p7 | 11:108080520 | CTTGCCTCAGCCTCC[A/T]GAGTAGCTGGGACTA | 8065 |
rs139325787 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CUL5 | GRCh38.p7 | 11:108075800 | TCTGGGATTATAGAC[A/G]TGAGCCACCACCCCT | 8065 |
rs139341303 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | CUL5 | GRCh38.p7 | 11:108036719 | TTGACCTCAAAGTTA[C/T]CTGCCCACCTTGGCC | 8065 |
rs139413804 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108085902 | CGCAACCCTCTGAAT[A/G]TACTTTAAAAGCACT | 8065 |
rs139415234 | snp | A/G | 0.0185938 | 0.0946107 | upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108007984 | TTGGCCAGGCTGGTC[A/G]CGGACTCCTGACCGC | 8065 |
rs139433055 | snp | C/T | 0.0138799 | 0.0821421 | utr-variant-3-prime, intron-variant | CUL5 | GRCh38.p7 | 11:108104926 | TTAAGTATTTAATAG[C/T]ATCAAATTGTTCAAA | 8065 |
rs139460863 | snp | C/G/T | 0.000150489 | 0.00867315 | synonymous-codon | CUL5 | GRCh38.p7 | 11:108073446 | TAGATTTAGTAAACT[C/G/T]GTCAAAGAAGCTTTT | 8065 |
rs139473027 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108091560 | CTGGGTGTGATGGCA[C/T]GCACCTTAGTCCCAG | 8065 |
rs139508804 | snp | A/G | 0.029116 | 0.117091 | intron-variant | CUL5 | GRCh38.p7 | 11:108012683 | CTCACTGCAACCTCC[A/G]CCTCCCAGGTTCAAG | 8065 |
rs139515970 | snp | A/C/T | 0.00199481 | 0.0315187 | intron-variant | CUL5 | GRCh38.p7 | 11:108028195 | AATGTATAATAGATA[A/C/T]GTTAAATGTAATACA | 8065 |
rs139595157 | snp | A/G/T | 0.00517822 | 0.0506191 | intron-variant | CUL5 | GRCh38.p7 | 11:108079597 | TTGAATTTAATGTTT[A/G/T]TGTTTTTAGGCAAAA | 8065 |
rs139611417 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | CUL5 | GRCh38.p7 | 11:108085085 | GAGGTGTATACCAAA[G/T]AGAAATGAAAACATA | 8065 |
rs139675329 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | CUL5 | GRCh38.p7 | 11:108075282 | TCTACAGTGAGCTAC[G/T]TGAACTTAATTCTGC | 8065 |
rs139693510 | snp | A/G | 1.64999e-05 | 0.00287222 | missense | CUL5 | GRCh38.p7 | 11:108070175 | AAGGCATGATCAAGA[A/G]AAATGAAACTGAAAG | 8065 |
rs139733447 | in-del | -/AAGACCA | 0.00517822 | 0.0506191 | intron-variant | CUL5 | GRCh38.p7 | 11:108103357 | TGAGTCTGGGGGTTC[-/AAGACCA]AAGACCAACCTGGAC | 8065 |
rs139857473 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CUL5 | GRCh38.p7 | 11:108061182 | TACAAGGTGAGAGAG[A/G]TGGCTTATCACTATA | 8065 |
rs139890728 | snp | C/T | 0.029116 | 0.117091 | intron-variant | CUL5 | GRCh38.p7 | 11:108058539 | AGACGTGAGCCACTG[C/T]ACCCGGCCCAAAGTG | 8065 |
rs139897854 | snp | A/G | 0.0387552 | 0.1337 | intron-variant | CUL5 | GRCh38.p7 | 11:108072100 | GGGAGGATTGCTTGC[A/G]CCCAAGAGGTCAAGG | 8065 |
rs139963852 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108018795 | TTATGAATCCCCTAT[A/G]GATGCAAGTAGTGTA | 8065 |
rs140026086 | snp | G/T | 0.0337553 | 0.125452 | intron-variant | CUL5 | GRCh38.p7 | 11:108062275 | ACTTGGCTTCCTCTT[G/T]GAATAGAATCTCCTG | 8065 |
rs140051908 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108039753 | ACTGTTTTTTAATGG[A/G]CTTGGTTATTCAGTT | 8065 |
rs140068615 | snp | A/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108042014 | AAGATGATGGGGACT[A/T]TCATGGTAATGGGAG | 8065 |
rs140101768 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108038376 | TTGCTACAGTTAGTG[A/G]CCTCAACATGATGTT | 8065 |
rs140109459 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | CUL5 | GRCh38.p7 | 11:108103035 | TCCTGGACTCAAGCA[A/G]TCCACCCACATCACC | 8065 |
rs140141300 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108098254 | TACATAGAGTTTGTT[C/T]TAAAGCAATATGTAG | 8065 |
rs140175655 | snp | G/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108028610 | TTCGGAGGCCGAAGC[G/T]GGCGGATCACAAGGT | 8065 |
rs140188543 | snp | A/G | 0.00151453 | 0.0274768 | synonymous-codon | CUL5 | GRCh38.p7 | 11:108094408 | AGTTGGTATGCCAGC[A/G]GATTATGTAAACAAG | 8065 |
rs140221898 | in-del | -/ATTAA | 0.116488 | 0.211364 | intron-variant | CUL5 | GRCh38.p7 | 11:108078399 | CATTTATAATTTTTT[-/ATTAA]ATTATTTTACAATAC | 8065 |
rs140231568 | snp | C/T | 0.0295035 | 0.117819 | intron-variant | CUL5 | GRCh38.p7 | 11:108068090 | CCCACCATGCCCGGC[C/T]AATTTTTAGTAGAGA | 8065 |
rs140242208 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CUL5 | GRCh38.p7 | 11:108069955 | CATATCCATCTTCAA[C/T]AATCCTATAGTTAAG | 8065 |
rs140318499 | snp | A/T | 0.00835141 | 0.0640778 | intron-variant | CUL5 | GRCh38.p7 | 11:108034283 | TTGACAGCGTGTGAT[A/T]TGTTGTCTACCAGAG | 8065 |
rs140352337 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | CUL5 | GRCh38.p7 | 11:108030041 | ATGGTTCTTTCATAT[A/T]TGTTTATTTGCACAC | 8065 |
rs140454552 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CUL5 | GRCh38.p7 | 11:108093981 | GTGCTAGGATTACAC[A/G]CCATGCCAACTAATA | 8065 |
rs140462138 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | CUL5 | GRCh38.p7 | 11:108050680 | ACCTATACCCTTACT[A/G]GAAATTAAATTACTT | 8065 |
rs140523971 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108029451 | TGAAAGAATTCAAGA[A/G]GCTTTGTAGCAAGTT | 8065 |
rs140558057 | snp | A/C | 1.69269e-05 | 0.00290915 | intron-variant | CUL5 | GRCh38.p7 | 11:108088491 | ATTGCAAACATTAAT[A/C]ATTTTTCCATCAACT | 8065 |
rs140586272 | in-del | -/AAA | 0.406986 | 0.194565 | intron-variant | CUL5 | GRCh38.p7 | 11:108017390 | GCAAGACCCTGTCTC[-/AAA]AAAAAAAAAAAAAAA | 8065 |
rs140594110 | snp | A/G | 0.00517822 | 0.0506191 | upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108007668 | TAAGCATAAGCAAAG[A/G]GTGGCTTGGGTAGAT | 8065 |
rs140620822 | snp | A/G | 0.000198551 | 0.00996172 | synonymous-codon, intron-variant, utr-variant-5-prime | CUL5 | GRCh38.p7 | 11:108049922 | AGATGATACGGCTTT[A/G]CTAAAAGCATATATT | 8065 |
rs140657400 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CUL5 | GRCh38.p7 | 11:108076623 | TTTATCCATTGATGG[A/G]CGCTGAGGTTGTGTC | 8065 |
rs140681149 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108028675 | AACCCCGTCTCTACT[A/G]AAATACAAAAATTAG | 8065 |
rs140705501 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | CUL5 | GRCh38.p7 | 11:108009998 | CCAGATGACAACTGA[C/T]GAAGCGATACCATCG | 8065 |
rs140725296 | in-del | -/TTAT | | | intron-variant | CUL5 | GRCh38.p7 | 11:108080954 | CATGAAGATTTATCA[-/TTAT]TTATTTATTTATTTA | 8065 |
rs140748699 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | CUL5 | GRCh38.p7 | 11:108030549 | AGCTGAGGCAGGAGA[A/G]TCGCTTGAACCCGGG | 8065 |
rs140902042 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108064286 | ATTGAAATGAACATA[C/T]GGATTTTGTCTGCCA | 8065 |
rs140904336 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CUL5 | GRCh38.p7 | 11:108035393 | CCAGCCAGAATCCAT[A/G]ATGTTTTCATAGTTT | 8065 |
rs140915011 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108010130 | AAAAAGTTTGGAGAA[A/G]AATGAGGAAGACTTA | 8065 |
rs140949721 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | CUL5 | GRCh38.p7 | 11:108055872 | CTAAGCTCAGGTGAT[C/G]CACCTGCCTTGGCCT | 8065 |
rs141012811 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108067222 | CATAATGCCTGGTAC[A/G]AAGTAAGTGCCCATT | 8065 |
rs141019782 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | CUL5 | GRCh38.p7 | 11:108082657 | TTTTTTCTGTTTCTT[C/T]TTTTTCAGACAGGGT | 8065 |
rs141028279 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108032326 | AGCCTGGGAAATATA[A/G]CAAGACCCCATCTCT | 8065 |
rs141041139 | in-del | -/AAT | 0.00438332 | 0.0466095 | cds-indel | CUL5 | GRCh38.p7 | 11:108107067 | TGAGATAAATATTAG[-/AAT]ATTACTATTCCAATG | 8065 |
rs141065532 | in-del | -/TTTTTTTTG | 0.498794 | 0.0245311 | upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108007755 | TTTTTTGTTTGTAGT[-/TTTTTTTTG]TTTTTTTTGTTTTTT | 8065 |
rs141150246 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108081849 | ATGCTGGTGCCACAT[C/T]GTTGTGATTTACTGT | 8065 |
rs141151401 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | CUL5 | GRCh38.p7 | 11:108097279 | CCTCAGCTTCCCAAA[C/G]TGCTGGAATTACAGG | 8065 |
rs141257301 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CUL5 | GRCh38.p7 | 11:108047479 | TGCTTAGCAGTTGAA[A/G]ATTAAAACTGAGTTT | 8065 |
rs141264414 | snp | A/T | 0.00874735 | 0.0655527 | intron-variant | CUL5 | GRCh38.p7 | 11:108090523 | TAAATAGACTGCAGG[A/T]CAAATTATTATATCT | 8065 |
rs141264970 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108077041 | AAAATATGTTTGGCA[A/G]CTTCAGCATATAAGT | 8065 |
rs141266429 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CUL5 | GRCh38.p7 | 11:108060261 | TAGTGCCACTAATGA[C/T]AGTAGTACAGAAAGA | 8065 |
rs141324339 | snp | C/T | 0.000153988 | 0.00877328 | synonymous-codon, utr-variant-5-prime | CUL5 | GRCh38.p7 | 11:108046291 | GCATGCAGTCTGTCT[C/T]TGGGATGATAAAGGC | 8065 |
rs141329217 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CUL5 | GRCh38.p7 | 11:108054318 | TACCTTACTAATCTC[C/T]GTTTATGCAAATTCT | 8065 |
rs141360620 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108050192 | ATTGCTTTTCAGCTC[C/T]TAACTAGATTTTATT | 8065 |
rs141414443 | snp | G/T | 0.0138799 | 0.0821421 | intron-variant | CUL5 | GRCh38.p7 | 11:108079567 | TCCCTAAACACTTCA[G/T]CATACAGTCATTTAT | 8065 |
rs141483173 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | CUL5 | GRCh38.p7 | 11:108021165 | GTACATGCTGTTATT[G/T]TCACACAACGATGAA | 8065 |
rs141548810 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | CUL5 | GRCh38.p7 | 11:108064457 | TCACGCCTGTAATCC[C/T]AGCACATTAGGAGGC | 8065 |
rs141634842 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CUL5 | GRCh38.p7 | 11:108057479 | CATGCTGACATACCC[C/T]GTGATATGATGCACT | 8065 |
rs141671023 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108061526 | AAAATACTATAATGA[A/G]CGCTACCCCCATACC | 8065 |
rs141695840 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | CUL5 | GRCh38.p7 | 11:108068533 | ATGAATCCCCATTAC[C/T]TAAATTCAGCTTTAG | 8065 |
rs141732754 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108007543 | GAACTTATTGAAGTC[A/G]GAGTTGTAGCAGTGG | 8065 |
rs141765755 | snp | A/G | 0.0279526 | 0.114869 | intron-variant | CUL5 | GRCh38.p7 | 11:108098237 | ATCATGTTTAAGGAA[A/G]ATACATAGAGTTTGT | 8065 |
rs141838326 | snp | C/T | 0.0325976 | 0.123435 | intron-variant | CUL5 | GRCh38.p7 | 11:108041659 | GCAGTAGCGTGATCT[C/T]GGCTCACTGCAACCT | 8065 |
rs141974654 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108046870 | AAAGCTCATTTAGGC[A/G]TTAGATCAGTAATGC | 8065 |
rs142042507 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CUL5 | GRCh38.p7 | 11:108043980 | GTGAGCCAAGGTGGC[A/G]CCATTGCACTTCAGC | 8065 |
rs142045312 | in-del | -/AATT | 0.00874735 | 0.0655527 | intron-variant | CUL5 | GRCh38.p7 | 11:108029698 | AGTTTAATAGAAAAC[-/AATT]AATTATTAAATTCCT | 8065 |
rs142053067 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | CUL5 | GRCh38.p7 | 11:108081701 | AGCTTGCAGTGAGCT[A/G]AGATGGCGCTACTGC | 8065 |
rs142067045 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | CUL5 | GRCh38.p7 | 11:108042189 | GATGTGCTTATAGTC[C/T]ACTGCAGTTACCTTA | 8065 |
rs142110580 | snp | C/G | 0.0193772 | 0.0965046 | intron-variant | CUL5 | GRCh38.p7 | 11:108040360 | CTCATGCCGGTAATC[C/G]CAGCACTTTGGGAGG | 8065 |
rs142165792 | snp | C/T | 0.0138799 | 0.0821421 | utr-variant-3-prime, intron-variant | CUL5 | GRCh38.p7 | 11:108105891 | GAGTGCTTTCAAGAG[C/T]ATTTCGTAGGATCTG | 8065 |
rs142187359 | in-del | -/AGAT | 0.00676609 | 0.0577691 | intron-variant | CUL5 | GRCh38.p7 | 11:108047838 | AATTATGTTTATTTC[-/AGAT]AGATAGAGCTTTATT | 8065 |
rs142206248 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108039210 | TATTTAGTAGAGATG[G/T]GGTTTCTTCATGTTG | 8065 |
rs142277453 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108028871 | CTTCTTGCTCAGAAT[C/T]TTTTAATGGCTCTTC | 8065 |
rs142318682 | snp | C/T | 0.0322114 | 0.122752 | intron-variant | CUL5 | GRCh38.p7 | 11:108071334 | GGCACGATCACAATT[C/T]ACTGTAGCCTTGACC | 8065 |
rs142349205 | snp | A/G | 0.0023933 | 0.0345097 | utr-variant-3-prime, intron-variant | CUL5 | GRCh38.p7 | 11:108105727 | AAAGAATGGCTCAAC[A/G]TGGATTTTTATTCAT | 8065 |
rs142391106 | snp | A/G | 0.0325976 | 0.123435 | intron-variant | CUL5 | GRCh38.p7 | 11:108087822 | ATTCAAAAATTAGCC[A/G]GGCATGGTGGCGGGC | 8065 |
rs142400526 | snp | A/C/G/T | 0.00159649 | 0.0282165 | intron-variant | CUL5 | GRCh38.p7 | 11:108009872 | CTCCCACTCCACCCC[A/C/G/T]CTTCCTCCCTTTTCT | 8065 |
rs142411356 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CUL5 | GRCh38.p7 | 11:108025509 | TGTCCAGAATATCAC[C/T]CGGGGTAGGGCTACT | 8065 |
rs142427678 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | CUL5 | GRCh38.p7 | 11:108102528 | TAGAGATGGGGTTTC[A/G]CCATGTTGCCTAGGC | 8065 |
rs142478764 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | CUL5 | GRCh38.p7 | 11:108019665 | TGCTGTCACTCTTAT[A/T]AAAGTCTAGCACATA | 8065 |
rs142485715 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CUL5 | GRCh38.p7 | 11:108022633 | AGCCAATTAACACAG[A/G]ACCCAAACGCATTTT | 8065 |
rs142510230 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | CUL5 | GRCh38.p7 | 11:108012178 | ATATTATAATTTTAT[C/T]TTCTGTTTTAGATTA | 8065 |
rs142654572 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | CUL5 | GRCh38.p7 | 11:108075926 | TATCCACCATCTGAC[A/G]TAGTTACTCATTTTC | 8065 |
rs142772198 | snp | C/T | 0.0322114 | 0.122752 | intron-variant | CUL5 | GRCh38.p7 | 11:108083814 | GTAGAGTAAGTATCA[C/T]TAGCTGATCCAGGCA | 8065 |
rs142779232 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | CUL5 | GRCh38.p7 | 11:108015846 | ATTTTTCAGTAGATT[A/T]GAGGAGGGGAATTTT | 8065 |
rs142787597 | snp | C/T | 1.67063e-05 | 0.00289014 | synonymous-codon, utr-variant-5-prime | CUL5 | GRCh38.p7 | 11:108054919 | ACGAGCACTACGTTA[C/T]TTAGAAACAAGACGA | 8065 |
rs142804666 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108095033 | TTTCAGTTTGGATGA[A/C]AGTAGCAGGACTCCG | 8065 |
rs142812104 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | CUL5 | GRCh38.p7 | 11:108011779 | ACTACAGGCGCACGC[C/T]ACCACGCCCAGCTAA | 8065 |
rs142855630 | snp | C/T | 0.000591371 | 0.0171853 | intron-variant, upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108033793 | CCTTTTATCTTTTTT[C/T]TTTTCAAGAATAAAG | 8065 |
rs142914777 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | CUL5 | GRCh38.p7 | 11:108049096 | CCAATAATCCCAGAA[C/T]ATTTTCATCACCCTA | 8065 |
rs142923905 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | CUL5 | GRCh38.p7 | 11:108062037 | TCCCTGTCTCAACAC[A/G]TGGGAATTACAATTC | 8065 |
rs143051340 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | CUL5 | GRCh38.p7 | 11:108030687 | AAGCAGGCATCTGGA[A/G]CAAGACAGTATATTA | 8065 |
rs143057731 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant, utr-variant-3-prime | CUL5 | GRCh38.p7 | 11:108073913 | TCATGGGACTCCTTC[A/G]GGAGTTATGTTATAC | 8065 |
rs143096908 | snp | C/T | 0.0069818 | 0.0586699 | intron-variant | CUL5 | GRCh38.p7 | 11:108046221 | TTAAGATGTTTTGTT[C/T]AGTTCTTGTTTCATT | 8065 |
rs143133508 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108026476 | GAACTTCTCAGAGTC[A/G]TACGACATCTATCCT | 8065 |
rs143152474 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime, intron-variant | CUL5 | GRCh38.p7 | 11:108106030 | GGAAATTGGAATTTT[A/G]TTTAAAATTTTACAC | 8065 |
rs143178548 | in-del | -/AAAC | 0.0174175 | 0.0916809 | intron-variant | CUL5 | GRCh38.p7 | 11:108099893 | AAGGTTGAATAACTT[-/AAAC]AAAAAAAAAATTTTT | 8065 |
rs143183095 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | CUL5 | GRCh38.p7 | 11:108017587 | GGATGCGGAGGCTCA[C/T]GCCTGTAATTGCAGC | 8065 |
rs143219751 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108069601 | TAACTGAGTTATATT[C/T]AGTTAGCAGTGTAGG | 8065 |
rs143229252 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CUL5 | GRCh38.p7 | 11:108014098 | TGTTACCAACTGCTC[C/T]ATGCTCCCTCACAGA | 8065 |
rs143261006 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108059645 | GCACTTAGGGAGGCC[A/G]AGATGGGTGGATCAT | 8065 |
rs143283390 | in-del | -/AGTT | 0.0364509 | 0.129988 | intron-variant | CUL5 | GRCh38.p7 | 11:108089753 | TAAGAATATAGCGTC[-/AGTT]AGGCCGGGCGCACTG | 8065 |
rs143356961 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | CUL5 | GRCh38.p7 | 11:108075647 | CTCAAGCAATCCTCC[C/T]GCCTCAGCCACCTGA | 8065 |
rs143373958 | snp | A/T | 0.00676609 | 0.0577691 | intron-variant | CUL5 | GRCh38.p7 | 11:108078964 | TTATAATATTGATAT[A/T]TTTTAGAAGGGAATA | 8065 |
rs143480285 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | CUL5 | GRCh38.p7 | 11:108035986 | CCATATTTCAAGTCC[A/G]AGTGATCAGCGAGAC | 8065 |
rs143558482 | in-del | -/C | | | utr-variant-3-prime | CUL5 | GRCh38.p7 | 11:108106538 | TAAATGTACAGTTTT[-/C]TTTTTTTTTTTTTTT | 8065 |
rs143576238 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CUL5 | GRCh38.p7 | 11:108064006 | ATCTTCCTTTCCAAT[C/T]TGGATGCTCTTTCTT | 8065 |
rs143622405 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108056304 | ACATTCTAGCTTGCC[C/G]ATAATCAAATATTTT | 8065 |
rs143636535 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108100902 | GGTGTAGTGGTGCAT[A/G]CCTGTGGTCCCAGCT | 8065 |
rs143636791 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108052278 | CCTTCTTTACCATTA[A/T]GCTAAATATACTGCT | 8065 |
rs143648620 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | CUL5 | GRCh38.p7 | 11:108055516 | GAGTGCAGTGGTGCA[A/G]TTATACCTCACTGTA | 8065 |
rs143768517 | snp | A/G | 3.9275e-05 | 0.00443125 | synonymous-codon | CUL5 | GRCh38.p7 | 11:108094501 | GCACAAAAATAATAA[A/G]TTGGCATTACCAGGT | 8065 |
rs143803084 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | CUL5 | GRCh38.p7 | 11:108054505 | GTTTCTTATGGAGAA[A/G]GATTTTGTCTTATAT | 8065 |
rs143826017 | in-del | -/TCT | 0.197393 | 0.244402 | intron-variant | CUL5 | GRCh38.p7 | 11:108093276 | CTGTAATTTGGATGA[-/TCT]TCTAGCATTTTATCT | 8065 |
rs143862736 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108017532 | TTTTACTGGTAATTA[A/G]GGCGGTAGCGAAAAC | 8065 |
rs143867093 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | CUL5 | GRCh38.p7 | 11:108098721 | ATCTTGTCTCAATCA[A/G]TTTTTTAAAAATATA | 8065 |
rs143881541 | in-del | -/A | | | intron-variant | CUL5 | GRCh38.p7 | 11:108037116 | CCACCTGGAGGCAAG[-/A]AAAAAAAAAACAAAA | 8065 |
rs143946686 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108036199 | GTTTTCATGTTGTCT[C/G]TCTTTTTCCAGGGTC | 8065 |
rs143963393 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CUL5 | GRCh38.p7 | 11:108022792 | GGTGGTTCAAGACTA[C/T]AGTGAGCAGTGATGG | 8065 |
rs144008842 | snp | A/G | 0.0329836 | 0.124112 | intron-variant, upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108031986 | AGAACACATGAACAC[A/G]TAAAGGGGAACAACA | 8065 |
rs144098973 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CUL5 | GRCh38.p7 | 11:108035043 | GACTTACTGAGGTGT[A/G]TGTGTACCAGGAGGG | 8065 |
rs144127169 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | CUL5 | GRCh38.p7 | 11:108074695 | CGTGTAATTCCAGCT[A/G]CTTAGGAGACTGAGG | 8065 |
rs144140306 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | CUL5 | GRCh38.p7 | 11:108080785 | TCCGTATCAGATAGA[A/T]GATGTGCTAATATTT | 8065 |
rs144188707 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CUL5 | GRCh38.p7 | 11:108052904 | TGGCATACAAAGTTA[C/T]ATCTACTTTTTGTAC | 8065 |
rs144202793 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | CUL5 | GRCh38.p7 | 11:108048626 | GCCCAAACTCTAATA[A/G]TGGGGAAATAGACTC | 8065 |
rs144252250 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CUL5 | GRCh38.p7 | 11:108070386 | AAACTTAAATTTTAA[A/G]CATTTTCCCTCTTAG | 8065 |
rs144268936 | snp | A/C | 0.00119737 | 0.0244387 | upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108007225 | ACTGTGCTTGGCTGA[A/C]ATGCATAAATCTTAA | 8065 |
rs144354225 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | CUL5 | GRCh38.p7 | 11:108065551 | GTCAGCTGAGTTCAT[C/T]CTACTTTTGCTTTCT | 8065 |
rs144385228 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108097992 | ATTTCATCTTTCAGG[G/T]TGATATCTTTTTGTG | 8065 |
rs144407013 | in-del | -/C | 0.00199481 | 0.0315187 | intron-variant | CUL5 | GRCh38.p7 | 11:108094682 | TACAGATCTTTATTT[-/C]CAAAACAAAAGGACA | 8065 |
rs144411281 | snp | C/T | 0.0240643 | 0.107019 | intron-variant | CUL5 | GRCh38.p7 | 11:108013017 | TTTAACTTAATGATA[C/T]GGCTTACTCTTCTCT | 8065 |
rs144460308 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108102310 | TGGGATTACAGGCGT[C/G]AGCCACCATGCCCGG | 8065 |
rs144520409 | in-del | -/A | 0.195526 | 0.243993 | utr-variant-5-prime, upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108008994 | GGCCGCGGCGGGTGC[-/A]AACCACAAAGGCTAA | 8065 |
rs144537623 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CUL5 | GRCh38.p7 | 11:108052178 | GTCTTACTGTGTTGC[C/T]GAGGCTGGTCTCAAA | 8065 |
rs144594067 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CUL5 | GRCh38.p7 | 11:108064339 | TTGATCAATTTGTGT[A/G]TGTTGAACCATCCTT | 8065 |
rs144631477 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | CUL5 | GRCh38.p7 | 11:108057075 | TCTGATCTCCTACTG[C/T]AATTTGTATGTTAGT | 8065 |
rs144676450 | snp | C/T | | | utr-variant-3-prime, intron-variant | CUL5 | GRCh38.p7 | 11:108105784 | CAAATTATTTTATAT[C/T]TTATTTGATGTTAAG | 8065 |
rs144701983 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108033570 | AAGACCAGACTGTCT[A/C]CTTGGACAAGGCCAA | 8065 |
rs144709115 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108075578 | GTTCGCTGTGTCGCC[C/T]AGTCTGGAGTGCAGT | 8065 |
rs144744631 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | CUL5 | GRCh38.p7 | 11:108089912 | GGATGTGCTGGTGCA[C/G]TCCGGTAATTCCAGC | 8065 |
rs144754171 | in-del | -/C | 0.470034 | 0.11868 | intron-variant | CUL5 | GRCh38.p7 | 11:108042903 | GAGTACCTGGGACTA[-/C]AGGAGCGCACCACCA | 8065 |
rs144806887 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | CUL5 | GRCh38.p7 | 11:108028605 | GCACTTTCGGAGGCC[G/T]AAGCGGGCGGATCAC | 8065 |
rs144924223 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108009728 | GTTTCTTGTAAAGCA[A/G]TGTCTAAGACGCATC | 8065 |
rs144954642 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108054215 | CCATTTGTAATTTAC[C/T]ATTCTACCTTACCTT | 8065 |
rs144965632 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | CUL5 | GRCh38.p7 | 11:108093763 | CCCAGGCTGGAGCGC[A/G]GTGACACAATCAGAG | 8065 |
rs145017486 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108067269 | AATAATTTGTTTAAC[C/T]TCTCAAGCTAGAAAT | 8065 |
rs145021412 | snp | C/T | 0.0329836 | 0.124112 | intron-variant | CUL5 | GRCh38.p7 | 11:108043936 | GCTGAGGCAGGAGAA[C/T]CATTTGAACCCAGGA | 8065 |
rs145022963 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108089280 | CTGATATTTAGACCG[A/G]CTAACAATTTGGTTA | 8065 |
rs145033622 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | CUL5 | GRCh38.p7 | 11:108085988 | TTATTAATAAGCTTA[A/G]ATAATAAATAGCAAT | 8065 |
rs145096902 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | CUL5 | GRCh38.p7 | 11:108081890 | TAAGCTTTAAAAGCA[A/G]GATGTGTGCATGTTT | 8065 |
rs145113022 | snp | A/G/T | 0.000132027 | 0.00812389 | synonymous-codon, missense, utr-variant-5-prime | CUL5 | GRCh38.p7 | 11:108046348 | AGAAGATATTCTTGA[A/G/T]TTTATTAAGCAAGCA | 8065 |
rs145120147 | in-del | -/GAGAGA | 0.205078 | 0.245931 | intron-variant | CUL5 | GRCh38.p7 | 11:108061895 | CTTATGTGGCAGCAG[-/GAGAGA]GAGAGAGAGAGAGAG | 8065 |
rs145144739 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108050484 | CAATTCTCCTGCCTC[A/G]GCCTCCTGAGTAGCT | 8065 |
rs145197270 | in-del | -/CA | | | intron-variant | CUL5 | GRCh38.p7 | 11:108096116 | AAAAAAAAAATTATG[-/CA]CACACACACACACAC | 8065 |
rs145211549 | snp | A/T | 0.00517822 | 0.0506191 | utr-variant-3-prime, intron-variant | CUL5 | GRCh38.p7 | 11:108105364 | AATCTGTAGCATAGA[A/T]GTATTTTGGTATTTT | 8065 |
rs145216092 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CUL5 | GRCh38.p7 | 11:108027687 | GTTGGGATTACAAGC[A/G]TGAACTATTGCGCCT | 8065 |
rs145286512 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CUL5 | GRCh38.p7 | 11:108068149 | TCTTGAACTCCTGAC[C/T]TCAGGTGATCCGCCC | 8065 |
rs145312435 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CUL5 | GRCh38.p7 | 11:108048270 | AAAAAAAGTAAAAAT[A/G]ATAAACATAGGTGGA | 8065 |
rs145344038 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108024948 | GTGCTTTTATTCCAA[C/T]AGTCCACCTCCACTA | 8065 |
rs145345859 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CUL5 | GRCh38.p7 | 11:108070272 | TAAGTTGCTCTTAGT[C/T]AATTCTTTTCCACAT | 8065 |
rs145351218 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108066300 | AGTGAGCCAAGATCA[C/T]GCCACTGCACTCCAG | 8065 |
rs145412333 | snp | C/T | 0.030278 | 0.119257 | intron-variant | CUL5 | GRCh38.p7 | 11:108063118 | CCAAAGTGCTGGGAT[C/T]ACAGGTGTGAGCCAC | 8065 |
rs145516532 | snp | C/T | 0.0271762 | 0.113356 | intron-variant | CUL5 | GRCh38.p7 | 11:108091732 | ACACACACACACACA[C/T]GACAAATAATTAAAA | 8065 |
rs145523262 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CUL5 | GRCh38.p7 | 11:108030421 | CGTGGGCAGATCACC[C/T]GAGGTCGGGAGTTTG | 8065 |
rs145592882 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | CUL5 | GRCh38.p7 | 11:108042865 | CTTCCAGGGTTCAAG[C/T]GATTCCCTTGCCTTA | 8065 |
rs145598997 | in-del | -/A | | | intron-variant | CUL5 | GRCh38.p7 | 11:108063656 | AAATTAATAAAATTT[-/A]AAAAAAAATAAATAA | 8065 |
rs145693900 | snp | C/T | 0.0240643 | 0.107019 | intron-variant | CUL5 | GRCh38.p7 | 11:108028649 | AGAGACCAGCCTGGC[C/T]GACATGGTGAAACCC | 8065 |
rs145769859 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | CUL5 | GRCh38.p7 | 11:108025733 | GTACAGGTTAGTACT[C/T]AGCCACAGGCCTCAG | 8065 |
rs145855059 | snp | A/T | 0.000197666 | 0.00993951 | intron-variant | CUL5 | GRCh38.p7 | 11:108088677 | ACATGAATTTTTTGT[A/T]TTTCAACTTTTAAAA | 8065 |
rs145906107 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108083435 | AAGTGAGGATTGCTG[G/T]GTTTCTCTTAGTTTT | 8065 |
rs145955702 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | CUL5 | GRCh38.p7 | 11:108057573 | TGAGGAAAGATTAAA[C/G]AATCGCAAATTGATA | 8065 |
rs145974611 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108102559 | TGGTCTCAAACTCCA[C/T]GACTCAAACGATCCA | 8065 |
rs146027733 | snp | G/T | 0.0197687 | 0.0974348 | intron-variant | CUL5 | GRCh38.p7 | 11:108056468 | TTCTTTTAGTTTTTG[G/T]TTTGCTTGTCCTTGA | 8065 |
rs146070012 | in-del | -/CTTC | 0.0103295 | 0.0711199 | intron-variant | CUL5 | GRCh38.p7 | 11:108101888 | GAACACACTTTCCTT[-/CTTC]CTTCTTCCTCTCTGA | 8065 |
rs146077067 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | CUL5 | GRCh38.p7 | 11:108037667 | GGGAAGCTAATTAGG[G/T]GCTCAGCACCCAAAC | 8065 |
rs146077463 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108084098 | AAAGATTGGACACCC[A/C]TGCTTTAGAAGAATA | 8065 |
rs146095492 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108080487 | TGCAACATCCACCTC[C/G]TGGGTTCAAGTGATT | 8065 |
rs146196922 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | CUL5 | GRCh38.p7 | 11:108021577 | GCAGCCTTGAATTCC[C/T]GAGCTTAAGCAGTGC | 8065 |
rs146201529 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | CUL5 | GRCh38.p7 | 11:108064566 | AAATACAAAAATTAG[C/T]GGGCGAGGTGTCAGG | 8065 |
rs146221047 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | CUL5 | GRCh38.p7 | 11:108061527 | AAATACTATAATGAA[C/T]GCTACCCCCATACCC | 8065 |
rs146257959 | in-del | -/TTATTTATTTAT | | | intron-variant | CUL5 | GRCh38.p7 | 11:108080954 | CATGAAGATTTATCA[-/TTATTTATTTAT]TTATTTATTTATTTA | 8065 |
rs146320847 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108047030 | TTTCTATAACATGAG[G/T]TCTGGGACAGGGCAC | 8065 |
rs146339779 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | CUL5 | GRCh38.p7 | 11:108042411 | TTTTTTAGTAGAGAC[A/G]GGGTTTCACCATGTT | 8065 |
rs146396823 | snp | A/G | 0.000164867 | 0.00907779 | missense | CUL5 | GRCh38.p7 | 11:108097703 | AAGTCAACTCACCCA[A/G]AGACTTTACAGAAGG | 8065 |
rs146496136 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | CUL5 | GRCh38.p7 | 11:108038567 | GTAATTCCAGCTACT[C/T]GGGAGGCTGAGGCAG | 8065 |
rs146502041 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108025575 | CTCTACCCAATGCCT[A/G]GCACTTTAAAGGGTG | 8065 |
rs146622801 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CUL5 | GRCh38.p7 | 11:108013417 | AGATACCTTTGATGA[C/T]TCAAATTATTTGAGA | 8065 |
rs146623327 | snp | C/T | 3.44045e-05 | 0.00414741 | synonymous-codon | CUL5 | GRCh38.p7 | 11:108089605 | TGAAATTGAAGAAAA[C/T]ATGGTAGAGTGGCTA | 8065 |
rs146633062 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108092702 | GAGTGACTGTAAATA[C/G]TATGGGGTTTCTTTT | 8065 |
rs146669904 | in-del | -/A | 0.235564 | 0.249583 | intron-variant | CUL5 | GRCh38.p7 | 11:108023544 | GTTGTTTGAAAAAAG[-/A]AAAAAAAACAAAGAA | 8065 |
rs146701631 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | CUL5 | GRCh38.p7 | 11:108012848 | GCGATCCGCCTACCT[C/T]GGCCACCCAAAGTGT | 8065 |
rs146733548 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | CUL5 | GRCh38.p7 | 11:108040376 | CAGCACTTTGGGAGG[C/T]GAAGGCAGGTGGATC | 8065 |
rs146734335 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CUL5 | GRCh38.p7 | 11:108075739 | AGACAACATCTAGCT[A/G]TGTTGTTTGGGCTGG | 8065 |
rs146753263 | snp | A/C/G | 0.00169711 | 0.0290809 | intron-variant | CUL5 | GRCh38.p7 | 11:108072286 | TTTCTCTAAACTCTT[A/C/G]CTCTAGTAAATGAAA | 8065 |
rs146843253 | snp | A/C/G | 0.000247833 | 0.0111293 | synonymous-codon | CUL5 | GRCh38.p7 | 11:108094912 | GGAGGACTTGATACC[A/C/G]GAAGTAGAAGAATTC | 8065 |
rs146858716 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | CUL5 | GRCh38.p7 | 11:108009914 | CTTCCCTCCTAATTC[A/T]CCCATTCTTGAGTTC | 8065 |
rs146858776 | snp | C/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108058838 | TACAATTCTAATAAG[C/G]TTGATTATCACTCGC | 8065 |
rs146877430 | snp | A/C | 0.00794568 | 0.0625276 | intron-variant | CUL5 | GRCh38.p7 | 11:108054611 | AATACTGATTTTGAT[A/C]ATAATTGGAGTAATA | 8065 |
rs146932657 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108039791 | AATGTTATGACTGAT[A/G]TTCTTGCTTTTGTTG | 8065 |
rs146978624 | snp | A/G | 0.0256215 | 0.110247 | intron-variant | CUL5 | GRCh38.p7 | 11:108100802 | TTGGGAGGCCGAGGC[A/G]GGTGGATCACAAGGC | 8065 |
rs146980047 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108020048 | GCCCCCACCCCCACT[A/G]GCATTCATCTGTACA | 8065 |
rs147036503 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | CUL5 | GRCh38.p7 | 11:108019473 | TATACAGTCATTTAC[C/T]GCATATTGATGTTTT | 8065 |
rs147082996 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | CUL5 | GRCh38.p7 | 11:108077423 | GGCTGAGACAGGTGG[A/C]TCACTTGAGGTCAGG | 8065 |
rs147098920 | snp | G/T | 0.00795532 | 0.062565 | intron-variant, downstream-variant-500B | CUL5 | GRCh38.p7 | 11:108074531 | AAGTAAATAGGCCAG[G/T]TGCAGTGGCTCACGC | 8065 |
rs147114103 | in-del | -/GTAAA | 0.00478085 | 0.0486577 | intron-variant | CUL5 | GRCh38.p7 | 11:108022278 | TTGTATTATTTTGTT[-/GTAAA]GTAAGTGAATTATTT | 8065 |
rs147194027 | snp | A/T | | | intron-variant | CUL5 | GRCh38.p7 | 11:108080965 | ATCATTATTTATTTA[A/T]TTATTTATTTATTTA | 8065 |
rs147198848 | in-del | -/AAG | 0.00438332 | 0.0466095 | intron-variant | CUL5 | GRCh38.p7 | 11:108078837 | AAAATAACGTTTCTT[-/AAG]AAGGAAAAATAATCA | 8065 |
rs147206073 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108052591 | TGATTTCCTTTTTTG[A/G]TGTTTGTACATGATA | 8065 |
rs147222542 | snp | A/G | | | intron-variant | CUL5 | GRCh38.p7 | 11:108048286 | ATAAACATAGGTGGA[A/G]TCTTTTTTGTTTAAC | 8065 |
rs147312305 | snp | A/G | 0.0314385 | 0.121371 | intron-variant | CUL5 | GRCh38.p7 | 11:108036678 | AGACAGGTTTTCACC[A/G]TGTTGGCCGGGATGG | 8065 |
rs147315856 | snp | G/T | 0.00835141 | 0.0640778 | intron-variant, upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108032225 | AAAACAAACCAGATG[G/T]TCCTAGTTCAGTGGC | 8065 |
rs147410964 | snp | C/T | 0.000171157 | 0.00924927 | synonymous-codon, utr-variant-5-prime | CUL5 | GRCh38.p7 | 11:108054946 | ACGAGAATGTAACTC[C/T]GTTGAAGCAGTAAGT | 8065 |
rs147416748 | snp | A/G | 0.0295035 | 0.117819 | intron-variant | CUL5 | GRCh38.p7 | 11:108016869 | TGGATGCAGTGGCTC[A/G]TGCCCAACACTTTGG | 8065 |
rs147419422 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108090963 | ACTCTTACTGTCACT[C/T]ATAAGTATATAGGAA | 8065 |
rs147435565 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | CUL5 | GRCh38.p7 | 11:108085887 | TTATGGTGATGATTA[C/T]GCAACCCTCTGAATA | 8065 |
rs147523892 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CUL5 | GRCh38.p7 | 11:108069633 | TTACTGCCCTCCTCA[C/T]TCTCAATTAGACAGT | 8065 |
rs147540290 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108065852 | GCAGGAGGAATGATC[A/G]GTGGAAGCTTCTATT | 8065 |
rs147572093 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | CUL5 | GRCh38.p7 | 11:108043957 | GAACCCAGGAGGCGG[A/T]GGTTGCAGTGAGCCA | 8065 |
rs147588589 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CUL5 | GRCh38.p7 | 11:108040251 | TTGGGAGGCCGAGGC[C/T]GGAGGATTGCTTGAG | 8065 |
rs147588620 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CUL5 | GRCh38.p7 | 11:108086867 | ATTGATGTACATAGA[A/G]TTCATTTTTAATGAG | 8065 |
rs147591682 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | CUL5 | GRCh38.p7 | 11:108082376 | GTGTTGCCCTCCTGA[A/G]CTCGAGTAATCCTCC | 8065 |
rs147601710 | in-del | -/TGAC | 0.0322114 | 0.122752 | intron-variant | CUL5 | GRCh38.p7 | 11:108038887 | GATGTTAAGGTACAT[-/TGAC]TGAGATTTTCCCCCC | 8065 |
rs147676874 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | CUL5 | GRCh38.p7 | 11:108025003 | TGCTACCTCATTGTT[G/T]AATGTCTTATATCTG | 8065 |
rs147692319 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL5 | GRCh38.p7 | 11:108019598 | TGTAACGTAGTAGTG[C/T]AATAACACATCACTC | 8065 |
rs147695794 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108063250 | CTCTCTATTTCCATG[A/G]GTTCAATTGTTTTAA | 8065 |
rs147778972 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | CUL5 | GRCh38.p7 | 11:108081742 | GGGTGAGAGTGCGAG[C/T]CTCCGTCTCAAGAAA | 8065 |
rs147795626 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108076785 | GACTATTCAGGATTT[C/G]CTATTGAATCAGAAG | 8065 |
rs147855445 | snp | C/T | 0.00358779 | 0.0422022 | upstream-variant-2KB | CUL5 | GRCh38.p7 | 11:108007983 | GTTGGCCAGGCTGGT[C/T]GCGGACTCCTGACCG | 8065 |
rs147884125 | snp | C/T | 0.0333695 | 0.124785 | intron-variant | CUL5 | GRCh38.p7 | 11:108062748 | TCCAATTATATTCTT[C/T]TATTATTTTTAAACA | 8065 |
rs147903684 | snp | A/G | 0.00318978 | 0.0398085 | utr-variant-3-prime, intron-variant | CUL5 | GRCh38.p7 | 11:108105825 | AAAGTATGGTTTTTG[A/G]AGATAGTAGGAAATG | 8065 |
rs148002663 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108068210 | GGCTATGAGCCACCA[C/T]GCCCAGCCATGTGTA | 8065 |
rs148042253 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CUL5 | GRCh38.p7 | 11:108020091 | CACCATGACCCAACA[C/T]TTTTCATTAGGCCCA | 8065 |
rs148051994 | in-del | -/C/TC | | | intron-variant | CUL5 | GRCh38.p7 | 11:108080127 | TTTTTTTTTTTTTTT[-/C/TC]CCGGTATTCGTATAT | 8065 |
rs148057957 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL5 | GRCh38.p7 | 11:108064254 | GTTGAATTTTATCAG[A/G]TGCTTTTTCAGCATC | 8065 |
rs148114589 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CUL5 | GRCh38.p7 | 11:108047324 | CTGTCTCAAAAAAAG[A/G]CAAAAAAACAAAAAG | 8065 |
rs148172850 | snp | A/C | | | intron-variant | CUL5 | GRCh38.p7 | 11:108092107 | GTGCCACTGCACTGC[A/C]GCCTGGGCAACAGAG | 8065 |
rs148217233 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CUL5 | GRCh38.p7 | 11:108031019 | ATTCCATACAATCAC[C/T]GTATGCATCTCAGGT | 8065 |
rs148221010 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant, downstream-variant-500B | CUL5 | GRCh38.p7 | 11:108074237 | TTCGCTCTTGTTGCC[C/T]AGGCTTGAGTGCAAT | 8065 |
rs148268512 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, missense | CUL5 | GRCh38.p7 | 11:108106276 | AACAGGAAAAATTGC[C/T]GTCCATTTTAAAAAT | 8065 |
rs148272506 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | CUL5 | GRCh38.p7 | 11:108026921 | TTGAACTTGGGAGGC[A/G]GAGGTTGCAGTGAGC | 8065 |
rs148306132 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | CUL5 | GRCh38.p7 | 11:108014877 | AAAAGAGAGAGTGCT[C/T]GGTGCTCTTATTATT | 8065 |
rs148378345 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | CUL5 | GRCh38.p7 | 11:108079473 | TTGCTTTATCAAATA[C/T]GTTATCTCCTTATAT | 8065 |