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 |