SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs346807 | snp | C/T | 0.185788 | 0.241613 | intron-variant | UBE2O | GRCh38.p7 | 17:76411964 | CTGGGATTACAGGCG[C/T]GAGCCACTGTGCCTG | 63893 |
rs346808 | snp | A/G | 0.179105 | 0.239737 | intron-variant | UBE2O | GRCh38.p7 | 17:76409204 | cgatctcctgacctc[A/G]tgatctgccagcctc | 63893 |
rs346809 | snp | A/G | 0.171057 | 0.237209 | intron-variant | UBE2O | GRCh38.p7 | 17:76409198 | tgctctcgatctcct[A/G]acctcgtgatctgcc | 63893 |
rs346810 | snp | A/G | 0.179105 | 0.239737 | intron-variant | UBE2O | GRCh38.p7 | 17:76409032 | ggagtgcagtggcgc[A/G]atctcggctcactgc | 63893 |
rs346811 | snp | C/T | 0.171057 | 0.237209 | intron-variant | UBE2O | GRCh38.p7 | 17:76407844 | AACAGCAGCTCCACC[C/T]CACCAGGATGCTGCC | 63893 |
rs346816 | snp | C/T | 0.182296 | 0.240658 | intron-variant | UBE2O | GRCh38.p7 | 17:76394857 | AAATTAATTATATTA[C/T]GATTACTCCTCAAGC | 63893 |
rs346817 | snp | C/T | 0.125269 | 0.216661 | intron-variant | UBE2O | GRCh38.p7 | 17:76400405 | AGCAACCCAGGGGCA[C/T]GCGTGGGACAGGGCT | 63893 |
rs369654 | snp | C/T | 0.179105 | 0.239737 | intron-variant | UBE2O | GRCh38.p7 | 17:76420065 | CCACAGCTCATGATC[C/T]GGAGCCTCACCCCTA | 63893 |
rs372126 | snp | A/G | 0.251578 | 0.249995 | intron-variant | UBE2O | GRCh38.p7 | 17:76417134 | GGCCCTTCCGGCTAC[A/G]GCTCCAGAGCTTGTC | 63893 |
rs372558 | snp | C/G | 0.498908 | 0.0233371 | intron-variant | UBE2O | GRCh38.p7 | 17:76422094 | TGGTGATGTTTTTGA[C/G]ACCTCTATGTGTGAT | 63893 |
rs377253 | snp | C/G | 0.179744 | 0.239925 | intron-variant | UBE2O | GRCh38.p7 | 17:76417073 | CCCCTGATGAGGCAT[C/G]TGGTGCCCAGAGATG | 63893 |
rs381774 | snp | A/G | 0.178785 | 0.239642 | intron-variant | UBE2O | GRCh38.p7 | 17:76415706 | GCTACTTAGGAGGCC[A/G]AGGTAGGAGAATTGC | 63893 |
rs389809 | snp | A/G | 0.0829062 | 0.185956 | intron-variant | UBE2O | GRCh38.p7 | 17:76417915 | AGGACTCAAATACCA[A/G]CGGAAACAGCACCAT | 63893 |
rs394873 | snp | A/G | 0.499897 | 0.00718776 | intron-variant | UBE2O | GRCh38.p7 | 17:76417367 | TTCCCTGGAGAAGAC[A/G]ATAACATTTACAAAG | 63893 |
rs404014 | snp | G/T | 0.0836354 | 0.186609 | intron-variant | UBE2O | GRCh38.p7 | 17:76418204 | CAGCCTTCTGACAAT[G/T]TTTTCTATACTATTA | 63893 |
rs423130 | snp | C/T | 0.172674 | 0.237741 | intron-variant | UBE2O | GRCh38.p7 | 17:76420107 | TTTGGGGGAGTGTGG[C/T]GCGAAGGGGGCCACT | 63893 |
rs435892 | snp | A/T | 0.17332 | 0.23795 | intron-variant | UBE2O | GRCh38.p7 | 17:76402424 | ATCTGCCGTGGCCTA[A/T]TTCTGTTGCTCAGTT | 63893 |
rs443112 | snp | A/G | 0.179744 | 0.239925 | intron-variant | UBE2O | GRCh38.p7 | 17:76417817 | CATGGATGCATCAGC[A/G]TCCGCGAAGAGACGT | 63893 |
rs444896 | snp | A/G | 0.180064 | 0.240019 | intron-variant | UBE2O | GRCh38.p7 | 17:76425254 | AAAAAAAAAAAAGTA[A/G]AAGAAAAAAATGTGG | 63893 |
rs445683 | snp | A/G | 0.499965 | 0.00419314 | intron-variant | UBE2O | GRCh38.p7 | 17:76405440 | GAGCCTGCCCACCTC[A/G]CACTCTGCATGTGGG | 63893 |
rs447921 | snp | A/G | 0.219049 | 0.248077 | intron-variant | UBE2O | GRCh38.p7 | 17:76418477 | TGAATTGAATATCTA[A/G]ACTTCCTCCAACTGT | 63893 |
rs452868 | snp | A/C | 0.17332 | 0.23795 | intron-variant | UBE2O | GRCh38.p7 | 17:76425401 | aaggcttaacaaaaa[A/C]aggcagtcccccatc | 63893 |
rs453116 | snp | G/T | 0.179425 | 0.239831 | intron-variant | UBE2O | GRCh38.p7 | 17:76405722 | GCTGGTCGGAGGTGT[G/T]TGCGGTCTGTGAAGA | 63893 |
rs454879 | snp | A/C | 0.375 | 0.216506 | intron-variant | UBE2O | GRCh38.p7 | 17:76418574 | TCAAAAAAAAAAAAA[A/C]AAAACCTGTTCCTCC | 63893 |
rs493035 | snp | A/G | 0.179105 | 0.239737 | intron-variant | UBE2O | GRCh38.p7 | 17:76445075 | AGCAGCTCCGATGAT[A/G]TTCTTCCTCCTCCTT | 63893 |
rs495055 | snp | C/T | 0.179425 | 0.239831 | intron-variant | UBE2O | GRCh38.p7 | 17:76444808 | TTATTTAAGGGATTC[C/T]GAGGGCCCTGAAGGT | 63893 |
rs500466 | snp | A/T | 0.375 | 0.216506 | intron-variant | UBE2O | GRCh38.p7 | 17:76434794 | TTTGTTTGTTTTTTT[A/T]AAAAAAAAAAAAAAA | 63893 |
rs546588 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | UBE2O | GRCh38.p7 | 17:76435803 | GACAGGCTGGTCTGT[C/T]GTGCCTTCAGCTCAG | 63893 |
rs560924 | snp | A/G | 0.178785 | 0.239642 | intron-variant | UBE2O | GRCh38.p7 | 17:76420349 | GCTATGGAGGAGCAG[A/G]GGGCTATGGAAGTGC | 63893 |
rs567009 | snp | C/T | 0.483491 | 0.0893421 | intron-variant | UBE2O | GRCh38.p7 | 17:76438735 | GAAACACTGGTTATG[C/T]TGGTCTTACTGATGG | 63893 |
rs568020 | snp | C/T | 0.14933 | 0.228835 | intron-variant | UBE2O | GRCh38.p7 | 17:76438612 | AGAACAGTAATAAAG[C/T]TTTCAATTATTAGAG | 63893 |
rs579983 | snp | A/T | 0.100944 | 0.200705 | intron-variant | UBE2O | GRCh38.p7 | 17:76442459 | CCTCCCACTTACTAC[A/T]AATAGTATTCTTAGT | 63893 |
rs619907 | snp | C/T | 0.179425 | 0.239831 | intron-variant | UBE2O | GRCh38.p7 | 17:76449694 | TGACCTCAGGTGATC[C/T]GCCCGCCTCGGCCTC | 63893 |
rs669228 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | UBE2O | GRCh38.p7 | 17:76441530 | GTACGTCTTTGGTTC[A/G]AGGCTTTTTCTCTCC | 63893 |
rs679396 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | UBE2O | GRCh38.p7 | 17:76445228 | GACTGCCTTTTTTTT[C/T]TTCTTTTTCCAAGCA | 63893 |
rs694251 | snp | C/T | 0.0364509 | 0.129988 | intron-variant | UBE2O | GRCh38.p7 | 17:76442857 | CCTGCACTGTGTAGC[C/T]TTCTCCCTGGTCTCC | 63893 |
rs898083 | snp | A/G | 0.499913 | 0.00658888 | intron-variant | UBE2O | GRCh38.p7 | 17:76416202 | TGTATATGTGTATAT[A/G]TGTGTGTATATGTAT | 63893 |
rs898084 | snp | G/T | 0.185311 | 0.241486 | downstream-variant-500B | UBE2O | GRCh38.p7 | 17:76389510 | TTTTTTTTTTTTTTT[G/T]TGTTGGCTCATTAGC | 63893 |
rs898085 | snp | A/G | 0.427727 | 0.175821 | intron-variant | UBE2O | GRCh38.p7 | 17:76397600 | TCGCTTCTCCCAGCA[A/G]TCTCTTCACGTCCAT | 63893 |
rs1000820 | snp | C/T | 0.121022 | 0.21416 | intron-variant | UBE2O | GRCh38.p7 | 17:76437641 | GCTGGCCTTGAACTC[C/T]TGGACCCAAGCGATC | 63893 |
rs1000821 | snp | C/T | 0.378765 | 0.214288 | intron-variant | UBE2O | GRCh38.p7 | 17:76437921 | AAGGAAGATGGGGGA[C/T]AGGCTAAATACACGC | 63893 |
rs1254663 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | UBE2O | GRCh38.p7 | 17:76437461 | tttttctttttcttt[C/T]tttttttttttgaga | 63893 |
rs1356533 | snp | G/T | 0.481009 | 0.0955756 | intron-variant | UBE2O | GRCh38.p7 | 17:76447872 | AGGCACAGGGCTGGC[G/T]CTCTCTGACAGACAT | 63893 |
rs1356534 | snp | A/G | 0 | 0 | intron-variant | UBE2O | GRCh38.p7 | 17:76427634 | TTGTTCTGCAAGCAA[A/G]AAGCTTCAGGGGTAT | 63893 |
rs1466003 | snp | A/G | 0.422787 | 0.180679 | intron-variant | UBE2O | GRCh38.p7 | 17:76439277 | AGGACTGTAAATAAC[A/G]ATAACAACAAAGGTT | 63893 |
rs1533570 | snp | C/T | 0.477345 | 0.103991 | intron-variant | UBE2O | GRCh38.p7 | 17:76425895 | TTCCTCTGCCGCTCA[C/T]CTGTGTCAGATCCCG | 63893 |
rs1550767 | snp | A/G | 0.079617 | 0.182947 | intron-variant | UBE2O | GRCh38.p7 | 17:76432281 | TGGATTGACAGGAAC[A/G]TACTTTGATAACTGA | 63893 |
rs1674350 | snp | A/G | 0.180064 | 0.240019 | intron-variant | UBE2O | GRCh38.p7 | 17:76416115 | TGCGTATGTGTATAC[A/G]TATATACATATATGT | 63893 |
rs1811459 | snp | C/T | 0.100944 | 0.200705 | intron-variant | UBE2O | GRCh38.p7 | 17:76443610 | CCCAAGTCTGTGGAC[C/T]TAAAAAAAAAAAAAT | 63893 |
rs1811460 | snp | A/C | 0.497933 | 0.032082 | intron-variant | UBE2O | GRCh38.p7 | 17:76443601 | GTGGACTTAAAAAAA[A/C]AAAAAATGTTCTGAC | 63893 |
rs1899996 | snp | A/C | 0.00438332 | 0.0466095 | | | GRCh38.p7 | 17:76443879 | TACCAGACTATACCA[A/C]ATGTTTCTCTTTTTT | 63893 |
rs1968767 | snp | A/T | 0.475081 | 0.108804 | intron-variant | UBE2O | GRCh38.p7 | 17:76424862 | TTCTttttttttttt[A/T]attttttattttttt | 63893 |
rs2009584 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76435417 | TGTGTGTGTGTGTGT[A/G]TGTGTGTGTGTGTGT | 63893 |
rs2958219 | snp | C/T | 0 | 0 | intron-variant | UBE2O | GRCh38.p7 | 17:76406744 | CCATTGCACTCCAGT[C/T]TGGGCAACACAGCGA | 63893 |
rs3135933 | snp | A/G | 0.497558 | 0.0348586 | intron-variant | UBE2O | GRCh38.p7 | 17:76449709 | GGATCACCTGAGGTC[A/G]GGAGTTCAAGAACAG | 63893 |
rs3219583 | microsatellite | (CA)19/20/21/22/23/24/25/26/27/30/31/32 | 0.83205 | 0.110663 | intron-variant | UBE2O | GRCh38.p7 | 17:76435403 | TTAAATATACAGATA[lengthTooLong]AAAGATTAAGATTTA | 63893 |
rs3744042 | snp | A/C | 0 | 0 | utr-variant-3-prime | UBE2O | GRCh38.p7 | 17:76390300 | TGGGCGTCACCCGGA[A/C]CCTAGCCTGGTCCCA | 63893 |
rs3744043 | snp | A/G | 0.0690024 | 0.172453 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76398853 | TCGCTTATCTACCAC[A/G]AAGTCTCCAGGGCAG | 63893 |
rs3803739 | snp | C/T | 0.497671 | 0.0340435 | missense | UBE2O | GRCh38.p7 | 17:76391203 | TAGCTGAGGCCAGGC[C/T]CTGGGCACCGCCCTC | 63893 |
rs3809691 | snp | C/G | 0.39457 | 0.203972 | intron-variant | UBE2O | GRCh38.p7 | 17:76400340 | TGGGCTGGACTCCTG[C/G]GAGGCCAGCAGTGTT | 63893 |
rs3809693 | snp | A/G | 0.453939 | 0.144598 | intron-variant | UBE2O | GRCh38.p7 | 17:76400945 | GCAGGAAGGAAAGGG[A/G]CAGCAGCTCAGCTCC | 63893 |
rs3833087 | in-del | -/C | | | utr-variant-3-prime | UBE2O | GRCh38.p7 | 17:76390543 | TTGTTGGCGCAACCC[-/C]ACACTTCATGCAAGG | 63893 |
rs4238986 | snp | A/G | 0.475789 | 0.107327 | intron-variant | UBE2O | GRCh38.p7 | 17:76415995 | catatgcacatacac[A/G]tatatacgtatgtgt | 63893 |
rs4238987 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | UBE2O | GRCh38.p7 | 17:76432004 | AGGCATGGATAAATC[A/C]ACACTTTACACACTC | 63893 |
rs4419085 | snp | C/T | 0.170408 | 0.236992 | intron-variant | UBE2O | GRCh38.p7 | 17:76447601 | CCCCCTCCTGGAGGA[C/T]GGCCGGGGTTACTTT | 63893 |
rs4422008 | snp | A/T | 0.488374 | 0.075352 | intron-variant | UBE2O | GRCh38.p7 | 17:76443295 | GGAATATATATATAT[A/T]TTTTTTTCCTCGAGA | 63893 |
rs4458029 | snp | A/G | 0.47709 | 0.104548 | intron-variant | UBE2O | GRCh38.p7 | 17:76415935 | catacacgtatatac[A/G]tatgcgtatacatat | 63893 |
rs4462625 | snp | A/G | 0.499937 | 0.0055907 | intron-variant | UBE2O | GRCh38.p7 | 17:76416744 | TCACTTCTTGGCTGG[A/G]TCATTAGGTCCTAAG | 63893 |
rs4516263 | snp | C/T | 0.489259 | 0.0724914 | intron-variant | UBE2O | GRCh38.p7 | 17:76436480 | CCAGCAATTTTTCTT[C/T]GGTGCTGGATTGTCA | 63893 |
rs4550478 | snp | C/T | 0.499902 | 0.00698814 | intron-variant | UBE2O | GRCh38.p7 | 17:76416736 | CCAAAATGTCACTTC[C/T]TGGCTGGGTCATTAG | 63893 |
rs4789291 | snp | G/T | 0.477684 | 0.103247 | intron-variant | UBE2O | GRCh38.p7 | 17:76410046 | TTACCAAGCAGGGAG[G/T]AGTAGCTGTCAAGGT | 63893 |
rs4789294 | snp | A/G | 0.471673 | 0.115589 | intron-variant | UBE2O | GRCh38.p7 | 17:76423095 | GGAGAACATCTGGCA[A/G]TGCAGGAAACAGGAA | 63893 |
rs4789295 | snp | A/C | 0.471578 | 0.115772 | intron-variant | UBE2O | GRCh38.p7 | 17:76423098 | GAACATCTGGCAATG[A/C]AGGAAACAGGAATCA | 63893 |
rs4789296 | snp | C/T | 0.485118 | 0.0849685 | intron-variant | UBE2O | GRCh38.p7 | 17:76444468 | CTTGAGCCCAGGAGG[C/T]GGAGGCTGCAGTAAG | 63893 |
rs4789297 | snp | A/C | 0.171057 | 0.237209 | intron-variant | UBE2O | GRCh38.p7 | 17:76451269 | CAATAACCCTCTTTT[A/C]CTGACACAATACTGG | 63893 |
rs4789298 | snp | C/T | 0.482008 | 0.0931261 | intron-variant, upstream-variant-2KB | AANAT, UBE2O | GRCh38.p7 | 17:76453976 | ATTAACTTATTTTCA[C/T]CTTAATTTGCTCATC | 63893 |
rs5822131 | in-del | -/ACTA | 0.17332 | 0.23795 | intron-variant | UBE2O | GRCh38.p7 | 17:76431652 | GGAAAAGAAAGACTA[-/ACTA]TTAGGGCCAGACACT | 63893 |
rs5822133 | in-del | -/C | | | intron-variant | UBE2O | GRCh38.p7 | 17:76441043 | TTGAATTTGGGTTGG[-/C]CTCCCACTTGCTATG | 63893 |
rs5822135 | in-del | -/T | 0.497933 | 0.032082 | intron-variant | UBE2O | GRCh38.p7 | 17:76443595 | TGCCCAGTCAGAACA[-/T]TTTTTTTTTTTTTAA | 63893 |
rs7207108 | snp | A/G | 0.465263 | 0.127129 | intron-variant | UBE2O | GRCh38.p7 | 17:76417803 | GGTGTTTGATGCTGC[A/G]TGGATGCATCAGCGT | 63893 |
rs7207792 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | UBE2O | GRCh38.p7 | 17:76442157 | CCAGCTCTAGCTAGC[C/T]CTAGCCTAGTCCACA | 63893 |
rs7207983 | snp | G/T | 0.427119 | 0.176434 | intron-variant | UBE2O | GRCh38.p7 | 17:76434992 | ATGGCAGAGCTGGGC[G/T]CTCCCTGCAGTGGCA | 63893 |
rs7209271 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76394863 | GGAGTAATCATAATA[C/T]AATTAATTTCAAAGT | 63893 |
rs7209978 | snp | A/G | 0.130008 | 0.219321 | intron-variant | UBE2O | GRCh38.p7 | 17:76444793 | AAGATGATGTCATCA[A/G]CCTTCAGGGCCCTCA | 63893 |
rs7210520 | snp | C/T | 0.466721 | 0.124627 | intron-variant, upstream-variant-2KB | AANAT, UBE2O | GRCh38.p7 | 17:76453958 | ataaaaataggcaca[C/T]tgattaacttatttt | 63893 |
rs7215770 | snp | A/T | 0.0785177 | 0.181917 | intron-variant | UBE2O | GRCh38.p7 | 17:76446023 | TCCTATTAAGTGAGA[A/T]AAGTGATAGCCTCTT | 63893 |
rs7219098 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | UBE2O | GRCh38.p7 | 17:76437652 | actcctggacccaag[C/T]gatcctccctctggc | 63893 |
rs7219520 | snp | C/G | 0.0547245 | 0.156101 | intron-variant | UBE2O | GRCh38.p7 | 17:76447045 | CCTGCCTGCCCACTG[C/G]CACAACTTCCACCTA | 63893 |
rs7219524 | snp | C/G | 0.479177 | 0.0998894 | intron-variant | UBE2O | GRCh38.p7 | 17:76446358 | AAAAGTGCTGGCCCC[C/G]AACAGGTTCCACTGG | 63893 |
rs7223304 | snp | C/T | 0.497121 | 0.0378299 | intron-variant | UBE2O | GRCh38.p7 | 17:76451008 | AACGGAGCATAACTG[C/T]AAACAAAGTTAACCA | 63893 |
rs7223553 | snp | A/G | 0.497586 | 0.0346604 | intron-variant | UBE2O | GRCh38.p7 | 17:76450810 | ATTTTTAGTAGAGAC[A/G]GGGTTTCTCCATGTT | 63893 |
rs7223992 | snp | C/T | 0.499908 | 0.00678851 | intron-variant | UBE2O | GRCh38.p7 | 17:76429765 | ATGCCTCATGCCTGG[C/T]CTCAGCACTCCAGGA | 63893 |
rs7225310 | snp | G/T | 0.436123 | 0.166908 | intron-variant | UBE2O | GRCh38.p7 | 17:76425307 | CTACTTGGCTCATAT[G/T]GTATTTTTTTAAATA | 63893 |
rs7503549 | snp | A/G | 0 | 0 | intron-variant | UBE2O | GRCh38.p7 | 17:76406818 | AATTCTCCCGTCTCA[A/G]CCTCCCGAGTAGGTG | 63893 |
rs8066058 | snp | A/T | 0.0547245 | 0.156101 | intron-variant | UBE2O | GRCh38.p7 | 17:76413909 | AATGGGGCCTCCTGT[A/T]GGAGCTGGACTCCTC | 63893 |
rs8071034 | snp | A/G/T | 0.0437457 | 0.141368 | intron-variant | UBE2O | GRCh38.p7 | 17:76415927 | cacatgcacatacac[A/G/T]tatatacgtatgcgt | 63893 |
rs8072743 | snp | A/G | 0.171057 | 0.237209 | intron-variant, upstream-variant-2KB | AANAT, UBE2O | GRCh38.p7 | 17:76454472 | cctgggcaacagagc[A/G]agactctgtctcaaa | 63893 |
rs8076732 | snp | C/T | 0.0788843 | 0.182262 | intron-variant, upstream-variant-2KB | AANAT, UBE2O | GRCh38.p7 | 17:76454542 | CTCTAGggccaggcg[C/T]ggtggctcatgcctg | 63893 |
rs8076798 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | UBE2O | GRCh38.p7 | 17:76416056 | gtgtacatatgtaca[C/T]acacgtatatacgta | 63893 |
rs8076935 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | UBE2O | GRCh38.p7 | 17:76416094 | acatatgtaCAtaca[C/T]gtatatgcgtatgtg | 63893 |