SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs12830 | snp | A/G | 0.43608 | 0.166955 | synonymous-codon | CUL2 | GRCh38.p7 | 10:35013777 | TGATGCAGAATCTTC[A/G]TTTTCATTAAATATG | 8453 |
rs15460 | snp | C/T | 0.4422 | 0.159872 | utr-variant-3-prime | CUL2 | GRCh38.p7 | 10:35009984 | NNNNNNNNAATGTAT[C/T]TTAAAGGACATAAAA | 8453 |
rs998658 | snp | A/G | 0.46845 | 0.121572 | intron-variant | CUL2 | GRCh38.p7 | 10:35119726 | CAGACATGCTACCAC[A/G]TCTGGCTCATTTTTC | 8453 |
rs1131510 | snp | A/G | 0.0633504 | 0.166319 | utr-variant-3-prime | CUL2 | GRCh38.p7 | 10:35010157 | TGCCACGTCATGAGC[A/G]TCAAAGAAAATGCCT | 8453 |
rs1131511 | snp | A/T | | | utr-variant-3-prime | CUL2 | GRCh38.p7 | 10:35010121 | TATTTCAAGCTCATG[A/T]CATTATGACATTTCT | 8453 |
rs1213387 | snp | A/C | 0.0722614 | 0.17581 | intron-variant | CUL2 | GRCh38.p7 | 10:35123456 | TTAGGATGAACTATA[A/C]TGGAAGTACCAGATG | 8453 |
rs1926554 | snp | A/G | 0.41833 | 0.184838 | intron-variant | CUL2 | GRCh38.p7 | 10:35056041 | GTAAAACAGTTGTGC[A/G]TTAAATAGTTACTTG | 8453 |
rs1926555 | snp | C/T | 0.268724 | 0.249298 | intron-variant | CUL2 | GRCh38.p7 | 10:35055980 | CTGGGGTTCAGGGCA[C/T]ACCTGAAAGGTGTGT | 8453 |
rs1926556 | snp | A/G | 0.41833 | 0.184838 | intron-variant | CUL2 | GRCh38.p7 | 10:35055979 | TGGGGTTCAGGGCAC[A/G]CCTGAAAGGTGTGTC | 8453 |
rs2001893 | snp | C/T | 0.463234 | 0.130503 | intron-variant | CUL2 | GRCh38.p7 | 10:35011695 | AGAATCGTACTCACT[C/T]ACAATTTCAGTATTA | 8453 |
rs2126984 | snp | A/G | 0.46865 | 0.121211 | intron-variant | CUL2 | GRCh38.p7 | 10:35121363 | CTCCCAAGTAGCAGC[A/G]ACTATAGGCACACCA | 8453 |
rs2148482 | snp | C/T | 0.439918 | 0.162576 | intron-variant | CUL2 | GRCh38.p7 | 10:35059982 | atgagccactgtgcc[C/T]ggctAAATTAGTACT | 8453 |
rs2148483 | snp | C/T | 0.205417 | 0.245993 | intron-variant | CUL2 | GRCh38.p7 | 10:35052373 | CACATCCTGAAGTTT[C/T]GCAGCTCTGCCCCAT | 8453 |
rs2182516 | snp | A/T | 0.205723 | 0.246048 | intron-variant | CUL2 | GRCh38.p7 | 10:35060274 | ttttgtccttttttt[A/T]attttttattttttg | 8453 |
rs2243807 | snp | C/G | 0.00914312 | 0.0669923 | intron-variant | CUL2 | GRCh38.p7 | 10:35104205 | TAATCCCAGCACTTA[C/G]GGATGCCGAGGAAGG | 8453 |
rs2244100 | snp | A/G | 0.483708 | 0.088773 | intron-variant | CUL2 | GRCh38.p7 | 10:35034708 | GAGGGTTATTGTTTT[A/G]GGTATTTGGGGCAGC | 8453 |
rs2244174 | snp | A/G | 0.00252146 | 0.0354176 | intron-variant | CUL2 | GRCh38.p7 | 10:35035148 | GATTAGGAGGAAAAC[A/G]TTGCAGTTTCCCACA | 8453 |
rs2384275 | snp | A/G | 0.462034 | 0.132445 | downstream-variant-500B | CUL2 | GRCh38.p7 | 10:35008214 | TGGGCTGTGTGCTAC[A/G]GCTTCTGCAGTGATG | 8453 |
rs2384276 | snp | A/G | 0.268452 | 0.249318 | downstream-variant-500B | CUL2 | GRCh38.p7 | 10:35008377 | CTCTCTTCCTCATGC[A/G]AGAGATGTTTCCTTT | 8453 |
rs2384280 | snp | C/T | 0.268452 | 0.249318 | intron-variant | CUL2 | GRCh38.p7 | 10:35015934 | CTTCCAGATGGCAAT[C/T]CTTTTACAATTATTC | 8453 |
rs2384281 | snp | C/T | 0.268724 | 0.249298 | intron-variant | CUL2 | GRCh38.p7 | 10:35036662 | CCTGTTTTTTGAGCA[C/T]TTTATATTTTGGATA | 8453 |
rs2384282 | snp | A/T | 0.0376037 | 0.131863 | intron-variant | CUL2 | GRCh38.p7 | 10:35037145 | ttctagaagtgttat[A/T]tttttaccttgtaca | 8453 |
rs2384283 | snp | A/G | 0.40595 | 0.195396 | intron-variant | CUL2 | GRCh38.p7 | 10:35037861 | AAACAAAAACAAAAA[A/G]CCTGATTAATGGCCG | 8453 |
rs2384284 | snp | G/T | 0.20511 | 0.245937 | intron-variant | CUL2 | GRCh38.p7 | 10:35038838 | ACTATTACTAAAATA[G/T]GCATTAAATCAAGGG | 8453 |
rs2384285 | snp | A/G | 0.20511 | 0.245937 | intron-variant | CUL2 | GRCh38.p7 | 10:35048288 | GCTTTAATGGAAGCC[A/G]ATTATAACAACAAAA | 8453 |
rs2384286 | snp | C/T | 0.205723 | 0.246048 | intron-variant | CUL2 | GRCh38.p7 | 10:35051028 | GACATAAAATAGTGT[C/T]TCCTTGGCCAGGCAC | 8453 |
rs2384287 | snp | A/G | 0.442385 | 0.15965 | intron-variant | CUL2 | GRCh38.p7 | 10:35051631 | aacaacaacaacaac[A/G]aaaaatagtgtctcc | 8453 |
rs2384288 | snp | C/T | 0.22813 | 0.249042 | intron-variant | CUL2 | GRCh38.p7 | 10:35054569 | TAATATCAATGGATA[C/T]TAAGTTAAAGTCAGT | 8453 |
rs2384289 | snp | A/G | 0.468249 | 0.121932 | intron-variant | CUL2 | GRCh38.p7 | 10:35054597 | AGTAGGAAAGCAAAT[A/G]ACTTGCAACTTTAGA | 8453 |
rs2490657 | snp | C/T | 0 | 0 | intron-variant | CUL2 | GRCh38.p7 | 10:35012719 | GGAGACAAATATTAA[C/T]TGCCATTTACTTTGA | 8453 |
rs2490658 | snp | A/T | 0.00914312 | 0.0669923 | intron-variant | CUL2 | GRCh38.p7 | 10:35101374 | TACTAATGAGGTCAA[A/T]GTGTGGTCTCCACAT | 8453 |
rs2490660 | snp | G/T | 0.497613 | 0.0344622 | intron-variant | CUL2 | GRCh38.p7 | 10:35089820 | GTTTGTGTGTGTGTG[G/T]GGGGGGGGGCATCTC | 8453 |
rs2490661 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35107846 | TGCCCAGGCTGGAGT[A/G]CAGTGGCGCGATCTA | 8453 |
rs2490662 | snp | G/T | 0 | 0 | intron-variant | CUL2 | GRCh38.p7 | 10:35060252 | TATTTTTTGAGGCAG[G/T]ATCTCACCTAGGCTG | 8453 |
rs2490663 | snp | C/T | 0.487241 | 0.0788465 | intron-variant | CUL2 | GRCh38.p7 | 10:35040807 | AGGATGTGCGCTCTT[C/T]AGAAGAATCTAATGC | 8453 |
rs2490664 | snp | A/G | 0.0704125 | 0.17392 | intron-variant | CUL2 | GRCh38.p7 | 10:35028634 | GTAGTTACTAATATT[A/G]ATACTAAAATGCTAA | 8453 |
rs2490665 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | CUL2 | GRCh38.p7 | 10:35014395 | GATACAGAAGTTGTT[A/G]TTCTAAAAATTGCCT | 8453 |
rs2505631 | snp | A/T | 0.487241 | 0.0788465 | intron-variant, downstream-variant-500B | CUL2, MIR3611 | GRCh38.p7 | 10:35079457 | ctgtgccagaaagca[A/T]tgagcctatttgaag | 8453 |
rs2505632 | snp | A/G | 0.257732 | 0.24988 | intron-variant | CUL2 | GRCh38.p7 | 10:35073590 | AAGAAAAAGAAAAAA[A/G]AAAAGAAAAGAAAAG | 8453 |
rs2505633 | snp | A/G | 0.266546 | 0.249452 | intron-variant | CUL2 | GRCh38.p7 | 10:35071629 | CGAGGTCAGGAGATC[A/G]AGACCATCCTGGCTA | 8453 |
rs2505634 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | CUL2 | GRCh38.p7 | 10:35070646 | TGACTGGGGTGGAAG[C/T]GTGTTTTTCATTAGA | 8453 |
rs2505635 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | CUL2 | GRCh38.p7 | 10:35066727 | AATTGATATTTGTTC[A/T]CATTGATTCACTAGC | 8453 |
rs2505642 | snp | A/T | 0.0225045 | 0.103662 | intron-variant | CUL2 | GRCh38.p7 | 10:35028570 | AGCAGATGATAGACT[A/T]ACTCAGAATAAGAGA | 8453 |
rs2891473 | snp | A/G | 0.270621 | 0.249148 | intron-variant | CUL2 | GRCh38.p7 | 10:35116109 | GCACTTTGGGAGGCC[A/G]AGGTGGGCAGATAAC | 8453 |
rs3065352 | in-del | -/TA/TATA | 0 | 0 | utr-variant-3-prime | CUL2 | GRCh38.p7 | 10:35009221 | ATATATATATATATA[-/TA/TATA]AAATAAACAAAATAA | 8453 |
rs3065383 | in-del | -/CCT/CCTA | 0 | 0 | intron-variant | CUL2 | GRCh38.p7 | 10:35048220 | ACATGCAAAACTCTA[-/CCT/CCTA]AGAGAGCTGTCATGA | 8453 |
rs3065413 | in-del | -/AC | | | intron-variant, upstream-variant-2KB | CUL2 | GRCh38.p7 | 10:35075683 | cacacacacacacac[-/AC]GCACGCTCCACattt | 8453 |
rs3740083 | snp | A/G | 0.444133 | 0.157519 | intron-variant | CUL2 | GRCh38.p7 | 10:35031455 | TTTCATTTGTATTTT[A/G]GTCAACTTTATTTCT | 8453 |
rs3780888 | snp | A/G | 0.253824 | 0.249971 | intron-variant | CUL2 | GRCh38.p7 | 10:35028389 | GTAAATATATGTGAA[A/G]TAACTGCTAGTAGAG | 8453 |
rs3780889 | snp | A/C/G | 0.52327 | 0.207721 | intron-variant | CUL2 | GRCh38.p7 | 10:35010787 | ATGCACTGAAGGAAA[A/C/G]GTATACAGTACTATG | 8453 |
rs4244993 | snp | A/G | 0.268995 | 0.249277 | utr-variant-3-prime | CUL2 | GRCh38.p7 | 10:35008755 | AATGCAATTGAATAA[A/G]CCAATTGTAAGACCC | 8453 |
rs4244994 | snp | A/T | 0.422315 | 0.181128 | intron-variant | CUL2 | GRCh38.p7 | 10:35050133 | CAAGACCATCCTGGC[A/T]AACATGGCAAAACCC | 8453 |
rs4582914 | snp | A/G | 0.0614824 | 0.164198 | intron-variant | CUL2 | GRCh38.p7 | 10:35050310 | TGGTGACAACAGTGC[A/G]AGACTCCGTCTCAAA | 8453 |
rs4598625 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35031482 | GAAACTTTTCTGTTC[A/G]CAACATACCTTTTGA | 8453 |
rs4934529 | snp | A/T | 0.405776 | 0.195535 | intron-variant | CUL2 | GRCh38.p7 | 10:35013448 | TTCGGAGAGAATGCA[A/T]AGTTACACATTCTAA | 8453 |
rs4934530 | snp | C/T | 0.26818 | 0.249338 | intron-variant | CUL2 | GRCh38.p7 | 10:35021769 | TGTGGGCTGTGATCG[C/T]GCACCTCCACTCCAG | 8453 |
rs4934531 | snp | C/T | 0.253824 | 0.249971 | intron-variant | CUL2 | GRCh38.p7 | 10:35021929 | AGTGGGGCGAGGGGG[C/T]ACCCGGCCCTATTAG | 8453 |
rs4934533 | snp | A/G | 0.464416 | 0.128553 | intron-variant | CUL2 | GRCh38.p7 | 10:35070691 | CACTCTCCAGCAAGC[A/G]CACTCTTCCCCCCAA | 8453 |
rs4934699 | snp | A/G | 0.405776 | 0.195535 | intron-variant | CUL2 | GRCh38.p7 | 10:35017648 | CAGTGAGCCAAGATC[A/G]CACCACTGCACTCAA | 8453 |
rs4934700 | snp | A/G | 0.406296 | 0.19512 | intron-variant | CUL2 | GRCh38.p7 | 10:35021914 | GGTGAGGTGGGGCGA[A/G]GTGGGGCGAGGGGGC | 8453 |
rs4934701 | snp | C/T | 0.26818 | 0.249338 | intron-variant | CUL2 | GRCh38.p7 | 10:35021974 | TTGAGATGTGATTTC[C/T]CCAGAAGACTTCCCT | 8453 |
rs4934702 | snp | C/T | 0.442113 | 0.159977 | intron-variant | CUL2 | GRCh38.p7 | 10:35034146 | ACTTAACTAAGTCAG[C/T]TGGATTTGAGTCTAC | 8453 |
rs4934704 | snp | C/T | 0.444533 | 0.157025 | intron-variant | CUL2 | GRCh38.p7 | 10:35043236 | TTTTTGACAGCCAGA[C/T]AGAGCAAAGTGCATG | 8453 |
rs4934705 | snp | C/T | 0.418169 | 0.184985 | intron-variant | CUL2 | GRCh38.p7 | 10:35045606 | TGTGGTCCCAGCTAC[C/T]CTGGAGGCTGAGGTG | 8453 |
rs4934706 | snp | C/T | 0.444931 | 0.15653 | intron-variant | CUL2 | GRCh38.p7 | 10:35045667 | GGCTACAGTGAGCCA[C/T]GATTGCACCACTGCA | 8453 |
rs4934707 | snp | C/G | 0.418007 | 0.185132 | intron-variant | CUL2 | GRCh38.p7 | 10:35045685 | TTGCACCACTGCACT[C/G]CAGCCTGGGTGACAG | 8453 |
rs4934708 | snp | A/C | 0.254944 | 0.249951 | intron-variant | CUL2 | GRCh38.p7 | 10:35047235 | GAAACCCTACCTCAA[A/C]CTCCATATTTGCTTA | 8453 |
rs4934709 | snp | A/C | 0.441841 | 0.160303 | intron-variant | CUL2 | GRCh38.p7 | 10:35050396 | CTATAGATACCTAGA[A/C]CGTAACAGAAACAAA | 8453 |
rs4934710 | snp | C/T | 0.41833 | 0.184838 | intron-variant | CUL2 | GRCh38.p7 | 10:35061488 | AAAAAATCACACTTA[C/T]AATGTAACCTAAAAT | 8453 |
rs4934711 | snp | A/G | 0.452088 | 0.147217 | intron-variant | CUL2 | GRCh38.p7 | 10:35071382 | TAGCAATAATTCCAT[A/G]AGCTTAGTTTTTTTG | 8453 |
rs4934712 | snp | A/G | 0.27008 | 0.249192 | intron-variant | CUL2 | GRCh38.p7 | 10:35071554 | GGACTACAGGCACCC[A/G]CCACCATGCCCAGCT | 8453 |
rs4934714 | snp | C/G | 0.0551013 | 0.156571 | intron-variant, upstream-variant-2KB | CUL2 | GRCh38.p7 | 10:35075887 | GAATTATAAAACGCA[C/G]CTACCATATGACCCA | 8453 |
rs4934715 | snp | G/T | 0.435119 | 0.16802 | intron-variant, upstream-variant-2KB | CUL2 | GRCh38.p7 | 10:35076064 | ttaaaatgcaatata[G/T]ccatacaataaatta | 8453 |
rs4934716 | snp | A/G | 0.446249 | 0.154875 | intron-variant, upstream-variant-2KB | CUL2, MIR3611 | GRCh38.p7 | 10:35080371 | TAAGGTTTGACCCAC[A/G]GAGCTCTAAGTACTC | 8453 |
rs4934717 | snp | C/T | 0.268724 | 0.249298 | intron-variant | CUL2 | GRCh38.p7 | 10:35082328 | ATGGTCCTATTTAAA[C/T]AAAAGTATGTATGTG | 8453 |
rs4934718 | snp | A/T | 0.433818 | 0.169443 | intron-variant | CUL2 | GRCh38.p7 | 10:35085422 | gcgacaaagcgagac[A/T]ccgtcccaaaaaaaa | 8453 |
rs4934719 | snp | C/T | 0.40595 | 0.195396 | intron-variant | CUL2 | GRCh38.p7 | 10:35087841 | TCTCAATCAGACCTC[C/T]CAGTTTAGAAGAGTT | 8453 |
rs4934720 | snp | C/T | 0.40595 | 0.195396 | intron-variant | CUL2 | GRCh38.p7 | 10:35087872 | CCAAAAGCCTTTTAA[C/T]GTATCTAAGAACAAA | 8453 |
rs4934721 | snp | A/G | 0.406123 | 0.195258 | intron-variant | CUL2 | GRCh38.p7 | 10:35088787 | TCCAAATACTCAAAA[A/G]GCAATTGAAAAGGAA | 8453 |
rs4934723 | snp | A/G | 0.40595 | 0.195396 | intron-variant | CUL2 | GRCh38.p7 | 10:35092835 | GGAAGACTAATGAAA[A/G]GCAGCAAGAATAGGA | 8453 |
rs4934724 | snp | C/T | 0.40595 | 0.195396 | intron-variant | CUL2 | GRCh38.p7 | 10:35104741 | GAATCAAAGACTTTT[C/T]TGGGGGGGGGACAGT | 8453 |
rs4934725 | snp | C/T | 0.40733 | 0.194287 | intron-variant | CUL2 | GRCh38.p7 | 10:35109308 | GGCAGAATTATACAT[C/T]TATGCATCCATCAAT | 8453 |
rs4934726 | snp | A/G | 0.256619 | 0.249912 | intron-variant | CUL2 | GRCh38.p7 | 10:35112416 | GCTTACTGTCTGGAG[A/G]GAGTTTTCAGGCTCC | 8453 |
rs4934729 | snp | C/T | 0.270621 | 0.249148 | intron-variant | CUL2 | GRCh38.p7 | 10:35118303 | GCAATAATTCTTTCA[C/T]ATGTTCTTTTTTTCC | 8453 |
rs4934730 | snp | A/G | 0.407502 | 0.194147 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | CREM, CUL2 | GRCh38.p7 | 10:35126627 | CCCTGAAGACCTGAC[A/G]ACAGCCGTTACTCTG | 8453 |
rs5784437 | in-del | -/TTTTTTT | 0 | 0 | intron-variant | CUL2 | GRCh38.p7 | 10:35011212 | TTTTTAATTTTTTAA[-/TTTTTTT]TTTTTTTTTTTTTTA | 8453 |
rs5784438 | in-del | -/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35012054 | AGTGAGTGCAAATAC[-/T]TTTTTTTTTTTTTTT | 8453 |
rs5784440 | in-del | -/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35117543 | TTTTTTTTTTTTTTT[-/T]AACTGCTGTAAAAGG | 8453 |
rs6481935 | snp | C/T | 0.463666 | 0.129795 | intron-variant | CUL2 | GRCh38.p7 | 10:35054031 | CCCATTTAATTGTTT[C/T]ACTCTGAATTTAATT | 8453 |
rs7069513 | snp | A/T | 0.0678174 | 0.1712 | intron-variant | CUL2 | GRCh38.p7 | 10:35024518 | CAAAAAAAGAGAAAA[A/T]TCAAGTGTCTGCTTT | 8453 |
rs7074266 | snp | A/G | 0 | 0 | intron-variant | CUL2 | GRCh38.p7 | 10:35027494 | CCTAGGTAAAAAAGA[A/G]ATGTAACAATTAAGA | 8453 |
rs7074917 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35021911 | tggggtgaggtgggg[C/T]gaagtggggcgaggG | 8453 |
rs7079205 | snp | C/T | 0.434398 | 0.168811 | intron-variant | CUL2 | GRCh38.p7 | 10:35035691 | ataatttcttaacaa[C/T]tgatggaaatttagg | 8453 |
rs7079249 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | CUL2 | GRCh38.p7 | 10:35046990 | TTTGCTTTTCCTATA[C/T]GAACTCTACCATTGG | 8453 |
rs7079498 | snp | C/T | 0.429238 | 0.174281 | intron-variant | CUL2 | GRCh38.p7 | 10:35086416 | cctcaacctccctag[C/T]agctgggattacagg | 8453 |
rs7084196 | snp | C/T | 0.4444 | 0.15719 | intron-variant | CUL2 | GRCh38.p7 | 10:35078233 | CAAAATGTCCACCCC[C/T]AAAAAACTTAAATTA | 8453 |
rs7095213 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | CUL2 | GRCh38.p7 | 10:35046848 | cagtgagccaagatc[A/G]tgccacggcattcta | 8453 |
rs7097545 | snp | C/T | 0.0611083 | 0.163768 | intron-variant | CUL2 | GRCh38.p7 | 10:35116595 | AATTTTCCTTATTTA[C/T]GATGTAAGAATATGA | 8453 |
rs7098557 | snp | C/G | 0.0279526 | 0.114869 | intron-variant | CUL2 | GRCh38.p7 | 10:35060141 | cggtgcacacctgtt[C/G]ttccagcaactgggg | 8453 |
rs7099036 | snp | C/T | 0.4444 | 0.15719 | intron-variant | CUL2 | GRCh38.p7 | 10:35060646 | ACAGAGCCATGCAAT[C/T]GAGTACAGTTTTACT | 8453 |