SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs1614 | snp | C/T | 0 | 0 | utr-variant-3-prime, intron-variant | UBE3B | GRCh38.p7 | 12:109536491 | CAAACTACCCCTCCT[C/T]GTCAAAAATCCACAT | 89910 |
rs1617 | snp | C/T | 0.197082 | 0.244335 | utr-variant-3-prime, intron-variant | UBE3B | GRCh38.p7 | 12:109536459 | AAGTTGATATTGGTG[C/T]TTATAAATCACTCTC | 89910 |
rs9985 | snp | A/T | 0.0329836 | 0.124112 | utr-variant-3-prime, intron-variant | UBE3B | GRCh38.p7 | 12:109536389 | TCAGCACAGGGAAGA[A/T]GGATCCCATCCTAAT | 89910 |
rs12679 | snp | C/T | 0.0864827 | 0.189109 | synonymous-codon, intron-variant | UBE3B | GRCh38.p7 | 12:109530622 | GGATATTCTGGCCTC[C/T]GACTTCACACCGGAT | 89910 |
rs14863 | snp | C/T | 0.269267 | 0.249256 | utr-variant-3-prime, intron-variant | UBE3B | GRCh38.p7 | 12:109536346 | CACGCTGGGCGGGTT[C/T]GTGCATACATGCGGG | 89910 |
rs717260 | snp | C/T | 0.0629771 | 0.165899 | intron-variant | UBE3B | GRCh38.p7 | 12:109484929 | tctctacaaaaaata[C/T]aaaaacttgctgtgc | 89910 |
rs729783 | snp | G/T | 0 | 0 | intron-variant | UBE3B | GRCh38.p7 | 12:109543184 | GGGAAATACAGAAGG[G/T]CTGCGTGTGCGTGTG | 89910 |
rs729784 | snp | G/T | 0.267091 | 0.249415 | intron-variant | UBE3B | GRCh38.p7 | 12:109543459 | AGTGTCTAGAGTGAA[G/T]GAGGTAATAGTCCTA | 89910 |
rs731178 | snp | A/G | 0.499683 | 0.0125759 | downstream-variant-500B | UBE3B | GRCh38.p7 | 12:109543873 | GTACCATCTCTGGCT[A/G]TGGGCTAGTTTTTCC | 89910 |
rs961269 | snp | C/T | 0.0402882 | 0.136092 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109477338 | CGGCCCCGCCTCCGC[C/T]CCCGGCTGGCGTGAG | 89910 |
rs1001382 | snp | C/T | 0.499683 | 0.0125759 | intron-variant, downstream-variant-500B | UBE3B | GRCh38.p7 | 12:109537126 | aagtgctaagattac[C/T]ggcatgagccaccat | 89910 |
rs1030066 | snp | C/T | 0.200492 | 0.245049 | intron-variant | UBE3B | GRCh38.p7 | 12:109541438 | ggcaggcaggaactg[C/T]tattcactactttac | 89910 |
rs1045255 | snp | C/G | 0.499673 | 0.0127754 | utr-variant-3-prime, intron-variant | UBE3B | GRCh38.p7 | 12:109536174 | CAGGCTTCTGGAAAA[C/G]AGTGTGTGCTCTACT | 89910 |
rs1045256 | snp | A/G | 0.267091 | 0.249415 | utr-variant-3-prime, intron-variant | UBE3B | GRCh38.p7 | 12:109536176 | GGCTTCTGGAAAAGA[A/G]TGTGTGCTCTACTTT | 89910 |
rs1045258 | snp | A/G | 0.225893 | 0.248835 | utr-variant-3-prime, intron-variant | UBE3B | GRCh38.p7 | 12:109536224 | GAATTTAAAGACAGG[A/G]ATGTATTAATATTAT | 89910 |
rs1045263 | snp | A/G | 0.268724 | 0.249298 | utr-variant-3-prime, intron-variant | UBE3B | GRCh38.p7 | 12:109536386 | CTGTCAGCACAGGGA[A/G]GATGGATCCCATCCT | 89910 |
rs1045582 | snp | G/T | 0.270621 | 0.249148 | utr-variant-5-prime, intron-variant, upstream-variant-2KB, nc-transcript-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109477922 | GTGCTGGGATCTGGC[G/T]TGTGTGCTCCAGGGG | 89910 |
rs1078423 | snp | A/C | 0.18989 | 0.242666 | intron-variant | UBE3B | GRCh38.p7 | 12:109532259 | AGCATCCGTAGAGTG[A/C]TTGGATGAGGTTGCA | 89910 |
rs1078424 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | UBE3B | GRCh38.p7 | 12:109532300 | GCTCGTCACAGTGTG[A/G]AAACACAAAAATGCT | 89910 |
rs1543895 | snp | C/T | 0.25634 | 0.24992 | intron-variant | UBE3B | GRCh38.p7 | 12:109482358 | cagagtggaataaga[C/T]aatggagactccaaa | 89910 |
rs1543896 | snp | A/C | 0.499437 | 0.0167637 | intron-variant | UBE3B | GRCh38.p7 | 12:109482266 | TCGGGTGATGGGTGC[A/C]CTAAAAGCCCAGACT | 89910 |
rs1543897 | snp | A/T | 0.49975 | 0.0111793 | intron-variant | UBE3B | GRCh38.p7 | 12:109537406 | AGAAGCCACTGGGAC[A/T]TCAGAGCTGCCGAGG | 89910 |
rs1558803 | snp | C/T | 0.0663309 | 0.169604 | intron-variant | UBE3B | GRCh38.p7 | 12:109528393 | TAATACATACAAATA[C/T]GATTTTCCTATCATT | 89910 |
rs2004358 | snp | G/T | 0.269267 | 0.249256 | intron-variant | UBE3B | GRCh38.p7 | 12:109539249 | TTTTGTTTTTGTGGG[G/T]TTTTTTTGTTTTTGA | 89910 |
rs2004359 | snp | A/C | 0.49941 | 0.0171624 | intron-variant | UBE3B | GRCh38.p7 | 12:109539088 | CCACCACACCCAGGT[A/C]ATTTTTGTATTTTTA | 89910 |
rs2010050 | snp | G/T | 0 | 0 | intron-variant | UBE3B | GRCh38.p7 | 12:109539000 | gatctgcccgcctca[G/T]cctcccaaagtgttc | 89910 |
rs2058807 | snp | A/G | 0.49941 | 0.0171624 | utr-variant-3-prime, intron-variant | UBE3B | GRCh38.p7 | 12:109535468 | AATAGGTCCGGGAAG[A/G]CTCTCTGGCAGCTCA | 89910 |
rs2241204 | snp | C/T | 0.278664 | 0.248351 | intron-variant, utr-variant-3-prime | UBE3B | GRCh38.p7 | 12:109534232 | CTCCTCCCTCCTCAC[C/T]GGTGCTGTGGCCGGT | 89910 |
rs2241205 | snp | C/T | 0.445592 | 0.155704 | intron-variant | UBE3B | GRCh38.p7 | 12:109531108 | ATGGGTATAGAGAGA[C/T]AGTCCCTGGTGAGTA | 89910 |
rs2241206 | snp | A/G | 0.195526 | 0.243993 | intron-variant | UBE3B | GRCh38.p7 | 12:109531043 | AACAGCAATTGTTTA[A/G]TATTTTGCTTATCTG | 89910 |
rs2241207 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | UBE3B | GRCh38.p7 | 12:109530981 | GTCATTTACTTCTAT[A/G]ATGAAAGGAAATAAA | 89910 |
rs2241208 | snp | C/G | 0.499982 | 0.00299515 | intron-variant | UBE3B | GRCh38.p7 | 12:109524990 | GACACAATCAAAGGG[C/G]GCGGAGGCTGCTACA | 89910 |
rs2241209 | snp | A/G | 0.0685596 | 0.171987 | intron-variant | UBE3B | GRCh38.p7 | 12:109524713 | AAGCAGGGTCTCTGC[A/G]GGAAGCTTCAAAGGC | 89910 |
rs2241210 | snp | C/T | 0.49962 | 0.0137727 | intron-variant | UBE3B | GRCh38.p7 | 12:109512339 | CCTTCCCTCCTCGTG[C/T]TGGCCCTCTGTGGGA | 89910 |
rs2241211 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | UBE3B | GRCh38.p7 | 12:109511777 | GCCTCCTAAGCTTCC[A/G]GCCCTCCGGTGGCTT | 89910 |
rs2241212 | snp | A/T | 0.499918 | 0.00638925 | intron-variant | UBE3B | GRCh38.p7 | 12:109501836 | ATCTCTACAAAAATT[A/T]AAAAAAAAAAAAAAT | 89910 |
rs2241213 | snp | C/T | 0.499673 | 0.0127754 | intron-variant | UBE3B | GRCh38.p7 | 12:109501052 | CTGCCTCCCTCCTCA[C/T]AGCTGGCTTGCAGGT | 89910 |
rs2241214 | snp | A/T | 0.151407 | 0.229738 | intron-variant | UBE3B | GRCh38.p7 | 12:109489882 | AACAAAAAAGTCTCT[A/T]GCCATAATGTGACCT | 89910 |
rs2241215 | snp | C/T | 0.499437 | 0.0167637 | intron-variant | UBE3B | GRCh38.p7 | 12:109487684 | CCAAAATAGAAGAGC[C/T]TCTCCTCAAAGAGCA | 89910 |
rs2270361 | snp | C/G | 0.270621 | 0.249148 | intron-variant | UBE3B | GRCh38.p7 | 12:109498089 | ACAGACAAGAACCCA[C/G]TTCTTTGGGCTACTA | 89910 |
rs2287184 | snp | A/G | 0.270892 | 0.249126 | intron-variant | UBE3B | GRCh38.p7 | 12:109532446 | ATAAATGGTTCTGAG[A/G]TTCCTGAGACCATCC | 89910 |
rs2287186 | snp | C/T | 0.0372196 | 0.131242 | intron-variant | UBE3B | GRCh38.p7 | 12:109522620 | CCCTCTCAGCTTGGC[C/T]CAGCTGCTGGCTCTT | 89910 |
rs2287187 | snp | A/G | 0.188946 | 0.24243 | intron-variant | UBE3B | GRCh38.p7 | 12:109522585 | TTTGGAAAGCATCTG[A/G]CTTCTCCAGGTTCCT | 89910 |
rs2287188 | snp | A/C | 0.0689305 | 0.172377 | intron-variant | UBE3B | GRCh38.p7 | 12:109522478 | CAGGCAGGGTCCCTG[A/C]AGCTCTGGAGCCCAC | 89910 |
rs2287189 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109513007 | AGCCACTTTTAGGGG[C/T]TGTTCAAGGACCAAA | 89910 |
rs2287190 | snp | C/T | 0.20111 | 0.245173 | intron-variant | UBE3B | GRCh38.p7 | 12:109512848 | CATAGCAGGGGCTCC[C/T]TCAAGGAAGGCACAT | 89910 |
rs2287191 | snp | A/G | 0.268452 | 0.249318 | intron-variant | UBE3B | GRCh38.p7 | 12:109493936 | TGGAAGGCTGAGGTG[A/G]GAGGATGGCTTGAGC | 89910 |
rs2287192 | snp | C/T | 0.268724 | 0.249298 | intron-variant | UBE3B | GRCh38.p7 | 12:109493789 | AGGAGTCAGTTAATA[C/T]GTGTAAAAGTTTTAG | 89910 |
rs2302702 | snp | A/G | 0.200801 | 0.245111 | intron-variant | UBE3B | GRCh38.p7 | 12:109483453 | GGCTCAAGAGCAGAG[A/G]GTGGGCAGGGACCTG | 89910 |
rs2879107 | snp | A/G | 0.49949 | 0.0159663 | intron-variant | UBE3B | GRCh38.p7 | 12:109515612 | gacctcaggtgatcc[A/G]cctgcctcggcctct | 89910 |
rs3180821 | snp | A/T | | | utr-variant-3-prime, downstream-variant-500B, intron-variant | UBE3B | GRCh38.p7 | 12:109536701 | ATTTGTACTTCAGCA[A/T]ATGATGGCTGCGTTC | 89910 |
rs3214386 | in-del | -/A | | | intron-variant | UBE3B | GRCh38.p7 | 12:109501822 | taaaaaaaaaaaaaa[-/A]ttagccaggcatggc | 89910 |
rs3214387 | in-del | -/A | | | intron-variant | UBE3B | GRCh38.p7 | 12:109480190 | TAAAAAAAAAAAAAA[-/A]CTCTTCAGCAGAGGC | 89910 |
rs3742018 | snp | A/G | 0.279068 | 0.248304 | intron-variant | UBE3B | GRCh38.p7 | 12:109511329 | ATAGAAAGACACATC[A/G]GGGCCCAGCTCTGAG | 89910 |
rs3742019 | snp | A/G | 0.00104045 | 0.0227847 | synonymous-codon, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109511237 | TTTTCTGTCCCTGTC[A/G]AGTTCTTGGAAGAGC | 89910 |
rs3815575 | snp | A/G | 0.44768 | 0.153045 | intron-variant, downstream-variant-500B | UBE3B | GRCh38.p7 | 12:109510100 | CGAAGGGCCTTTTAA[A/G]TCTAAGGAGCTTTGT | 89910 |
rs4388956 | snp | C/G | 0.0275645 | 0.114116 | intron-variant | UBE3B | GRCh38.p7 | 12:109515316 | AAAATATACTAGCAC[C/G]CACTGGTATATAGTA | 89910 |
rs4766476 | snp | A/G | 0.268452 | 0.249318 | intron-variant | UBE3B | GRCh38.p7 | 12:109496895 | CTTTGAAGAAGCACA[A/G]CTTACCTGTTTTTTT | 89910 |
rs4766606 | snp | C/G | 0.270621 | 0.249148 | intron-variant | UBE3B | GRCh38.p7 | 12:109496585 | tagccatcccagtgg[C/G]tgtacaggggtatct | 89910 |
rs4766607 | snp | C/T | 0.0433465 | 0.140692 | intron-variant | UBE3B | GRCh38.p7 | 12:109526067 | CAGTGTTTATTTAAC[C/T]GTCCTACTCTACTCC | 89910 |
rs4766608 | snp | C/T | 0.269538 | 0.249235 | intron-variant | UBE3B | GRCh38.p7 | 12:109533410 | ACAGCTGCAAGGGCC[C/T]GTCCTGGAAGAGCAG | 89910 |
rs4766609 | snp | A/G | 0.268452 | 0.249318 | utr-variant-3-prime, intron-variant | UBE3B | GRCh38.p7 | 12:109535492 | ACCTATTCCCGTCCT[A/G]TGCATTCACATTGGC | 89910 |
rs5800862 | in-del | -/C | | | intron-variant | UBE3B | GRCh38.p7 | 12:109504316 | GCATTCAGCCAAATG[-/C]CCCCTGGGAGGCAAA | 89910 |
rs5800863 | in-del | -/T | 0.5 | 0 | intron-variant | UBE3B | GRCh38.p7 | 12:109515360 | TTACTATTATTACTG[-/T]TTTTTTGTTGTTGTT | 89910 |
rs5800864 | in-del | -/G | 0.499816 | 0.0095829 | intron-variant | UBE3B | GRCh38.p7 | 12:109543379 | CGGCACGGGGTCAGC[-/G]GGCTGGTAACACAGC | 89910 |
rs6606727 | snp | A/T | 0.268452 | 0.249318 | intron-variant | UBE3B | GRCh38.p7 | 12:109503645 | CATGTCACAAATTCT[A/T]CGAAAACCTTATCTT | 89910 |
rs6606728 | snp | C/T | 0.268452 | 0.249318 | intron-variant | UBE3B | GRCh38.p7 | 12:109503646 | ATGTCACAAATTCTT[C/T]GAAAACCTTATCTTT | 89910 |
rs6606729 | snp | A/C | 0.41141 | 0.19091 | intron-variant | UBE3B | GRCh38.p7 | 12:109515120 | gggtttcaccgtgtt[A/C]gccaggatggtctcg | 89910 |
rs6606730 | snp | G/T | 0.377582 | 0.214995 | intron-variant | UBE3B | GRCh38.p7 | 12:109515182 | cctcccaaagtgctg[G/T]gattacaggcgtgag | 89910 |
rs7139074 | snp | A/G | 0.201418 | 0.245234 | intron-variant | UBE3B | GRCh38.p7 | 12:109504414 | tttgttttagaggta[A/G]aagatatgggtctta | 89910 |
rs7139198 | snp | C/T | 0.267364 | 0.249396 | intron-variant | UBE3B | GRCh38.p7 | 12:109526297 | GGGCCCTCTCATCTC[C/T]GGGAAGCTTTATTTC | 89910 |
rs7296040 | snp | C/T | 0.200801 | 0.245111 | intron-variant | UBE3B | GRCh38.p7 | 12:109484081 | GCTTTATGAGGTAAT[C/T]ACTGTCACCCTCACA | 89910 |
rs7298565 | snp | A/G | 0.499791 | 0.0102124 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109499729 | CGCTGTGCTACTGTC[A/G]GAAGTATGTGTCTCA | 89910 |
rs7298925 | snp | C/T | 0.228547 | 0.249078 | intron-variant | UBE3B | GRCh38.p7 | 12:109486901 | AGTACAGAAGCCGAA[C/T]GTGAGCACAGCTAGT | 89910 |
rs7307917 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109503508 | AAAAGGAAAAAGAAA[A/G]CCACTTTTAATTCCA | 89910 |
rs7310945 | snp | A/G | 0.268452 | 0.249318 | intron-variant | UBE3B | GRCh38.p7 | 12:109508207 | TTTAGGCACATGGTA[A/G]GGATTAAAAGACATA | 89910 |
rs7311187 | snp | C/T | 0.499703 | 0.0121769 | intron-variant | UBE3B | GRCh38.p7 | 12:109500102 | GTTCCTTCCATTCAG[C/T]TATGGACCTTATCAA | 89910 |
rs7311488 | snp | C/G | 0.268452 | 0.249318 | intron-variant | UBE3B | GRCh38.p7 | 12:109493100 | TAATAAACAATTGTG[C/G]CTTCATTTCATACTT | 89910 |
rs7312902 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | UBE3B | GRCh38.p7 | 12:109526591 | TTAAATTCAATTTGC[A/G]gccgggcacagtggc | 89910 |
rs7314631 | snp | C/T | 0.199564 | 0.24486 | intron-variant | UBE3B | GRCh38.p7 | 12:109510736 | TAGGAAGAGGTCTTT[C/T]AGCTGAGCTGAGCAA | 89910 |
rs7358739 | snp | C/T | 0.288906 | 0.246954 | intron-variant | UBE3B | GRCh38.p7 | 12:109505104 | GAGAGAATCCAAATA[C/T]AGGTTTTTTAGTCAA | 89910 |
rs7486178 | snp | A/G | 0.457504 | 0.139435 | intron-variant | UBE3B | GRCh38.p7 | 12:109542461 | catactattaatccc[A/G]tcctcaagatggtgt | 89910 |
rs7954512 | snp | A/G | 0.267091 | 0.249415 | intron-variant | UBE3B | GRCh38.p7 | 12:109539779 | CCTCTGCTGGGCTTC[A/G]CTCAGCCCCTGGTGT | 89910 |
rs7954766 | snp | C/G | 0.257176 | 0.249897 | intron-variant | UBE3B | GRCh38.p7 | 12:109539977 | ACTGGGATGGGGTCT[C/G]TGTCAGCTTATAGAC | 89910 |
rs7955932 | snp | A/G | 0.270621 | 0.249148 | intron-variant | UBE3B | GRCh38.p7 | 12:109503498 | TTGCAAAAAAAAAAG[A/G]AAAAAGAAAACCACT | 89910 |
rs7956536 | snp | C/T | 0.499673 | 0.0127754 | intron-variant | UBE3B | GRCh38.p7 | 12:109542711 | caaggaacgcaggga[C/T]ttccagccatcaccc | 89910 |
rs7956557 | snp | C/T | 0.267091 | 0.249415 | intron-variant | UBE3B | GRCh38.p7 | 12:109542779 | cagcctggagaggaa[C/T]caaccctgtgaatct | 89910 |
rs7956788 | snp | C/T | 0.499673 | 0.0127754 | intron-variant | UBE3B | GRCh38.p7 | 12:109523157 | CGGTCCTCTGACAGG[C/T]GTCATCAAGTCCGAG | 89910 |
rs7959161 | snp | A/G | 0.0329836 | 0.124112 | intron-variant, upstream-variant-2KB | UBE3B, KCTD10 | GRCh38.p7 | 12:109478848 | TTAAATAATCTGTGC[A/G]GTGTCTGATACACCG | 89910 |
rs7965599 | snp | C/T | 0.25801 | 0.249872 | intron-variant | UBE3B | GRCh38.p7 | 12:109515526 | aggcatgtgccacca[C/T]gcccagctaattcta | 89910 |
rs7965773 | snp | C/T | 0.267091 | 0.249415 | intron-variant | UBE3B | GRCh38.p7 | 12:109539802 | CCTGGTGTGCAGGCT[C/T]CCTGTGTGCCCACAC | 89910 |
rs7966629 | snp | C/T | 0.290718 | 0.246662 | intron-variant | UBE3B | GRCh38.p7 | 12:109533295 | CTTGAGAGAGATGTA[C/T]GGCGTGTGCCAGTTT | 89910 |
rs7966661 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | UBE3B | GRCh38.p7 | 12:109533366 | ACAGCAGTTACAACA[C/T]GGTAACAGACAGAGC | 89910 |
rs7971160 | snp | A/T | 0.268452 | 0.249318 | intron-variant | UBE3B | GRCh38.p7 | 12:109508946 | TCAGTCAATGTTCCT[A/T]GATATGCAGACATGA | 89910 |
rs7971760 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | UBE3B | GRCh38.p7 | 12:109537491 | TTAGGATCCAGTCAG[A/G]AAAGAACCCTGGAGA | 89910 |
rs7975756 | snp | G/T | 0.289424 | 0.246872 | intron-variant | UBE3B | GRCh38.p7 | 12:109540536 | GTGCAGGGTTACCAG[G/T]CAGGCTGCCTTCTCC | 89910 |
rs7976796 | snp | C/T | 0.268452 | 0.249318 | intron-variant | UBE3B | GRCh38.p7 | 12:109490208 | CAGTGGTGCTGGGAT[C/T]CCTTGAATGCTCTAC | 89910 |
rs7979816 | snp | A/G | 0.267091 | 0.249415 | intron-variant | UBE3B | GRCh38.p7 | 12:109539581 | CCATGCAGTCTTGCC[A/G]TGAACCACAGAGAAA | 89910 |
rs10437846 | snp | C/G | 0.239614 | 0.249784 | intron-variant | UBE3B | GRCh38.p7 | 12:109508947 | CAGTCAATGTTCCTT[C/G]ATATGCAGACATGAA | 89910 |
rs10466917 | snp | G/T | 0.45645 | 0.140991 | intron-variant | UBE3B | GRCh38.p7 | 12:109539659 | CATGGCTGTGATAAC[G/T]GTCATTATTTTGTTC | 89910 |
rs10675153 | in-del | -/TAAGAT | 0.499551 | 0.0149693 | intron-variant | UBE3B | GRCh38.p7 | 12:109519887 | AGCCTAACCCCTGAA[-/TAAGAT]ATCGGGGCACCATAG | 89910 |
rs10679640 | in-del | -/AA | | | intron-variant | UBE3B | GRCh38.p7 | 12:109526885 | AAAAAAAAAAAAAAA[-/AA]TTGATTTGCAAAATA | 89910 |
rs10694353 | in-del | -/AT | 0.287606 | 0.247155 | intron-variant | UBE3B | GRCh38.p7 | 12:109526883 | TCAAAAAAAAAAAAA[-/AT]AATTGATTTGCAAAA | 89910 |
rs10744826 | snp | C/G | 0.49975 | 0.0111793 | intron-variant | UBE3B | GRCh38.p7 | 12:109527707 | GGGAGGGACTGCCTG[C/G]AAGAGTAGAGAGGGC | 89910 |
rs10850234 | snp | A/C | 0.255782 | 0.249933 | upstream-variant-2KB, intron-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109476890 | CATTTTCCACCCCCA[A/C]ATGTCCGTTTTCAAT | 89910 |
rs10850240 | snp | A/C | 0.288127 | 0.247076 | intron-variant | UBE3B | GRCh38.p7 | 12:109481532 | GGTGTTTTTAAAAAA[A/C]CATTGGCATTGTAGT | 89910 |
rs10850274 | snp | A/G | 0.288127 | 0.247076 | intron-variant | UBE3B | GRCh38.p7 | 12:109497276 | TTGTGTTTATATTTC[A/G]AAACATTATACAATA | 89910 |
rs10850308 | snp | A/C | 0.321935 | 0.239427 | intron-variant | UBE3B | GRCh38.p7 | 12:109517903 | TACCTTGTTTGTGTC[A/C]CTCCTTACTGGAGAG | 89910 |
rs10850338 | snp | C/T | 0.289683 | 0.24683 | intron-variant | UBE3B | GRCh38.p7 | 12:109529127 | GATCGCACCACTGCA[C/T]TCCAGCCTGGGTGAC | 89910 |
rs10850339 | snp | A/T | 0.18989 | 0.242666 | intron-variant | UBE3B | GRCh38.p7 | 12:109529259 | TATGCTTTATGCAGT[A/T]GTAGTTGAGGGCACT | 89910 |
rs10850349 | snp | A/G | 0.333952 | 0.235483 | downstream-variant-500B | UBE3B | GRCh38.p7 | 12:109543991 | CAGCATCCTGAGGGG[A/G]TGTCGGCCTCTGTCT | 89910 |
rs11066813 | snp | A/G | 0.143284 | 0.226079 | intron-variant | UBE3B | GRCh38.p7 | 12:109480298 | ATAGGTACCTGATAA[A/G]CATCATCACATTTAG | 89910 |
rs11066816 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109480958 | GCCCTTTATTCACTT[C/T]TAAGGCATAAACGTT | 89910 |
rs11066838 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109482542 | ACTTCAAGTAAAGTA[A/G]CCTGGTAGAGAGATT | 89910 |
rs11066839 | snp | C/T | 0.228253 | 0.249052 | intron-variant | UBE3B | GRCh38.p7 | 12:109482696 | TCCGGGGGTCAGTGC[C/T]GTGTGCTTTAGGCTG | 89910 |
rs11066845 | snp | A/T | 0.115088 | 0.210473 | intron-variant | UBE3B | GRCh38.p7 | 12:109483356 | TGAGTTGCATGAAAG[A/T]GCCTATAGGAGGTAG | 89910 |
rs11066853 | snp | C/T | 0.0659589 | 0.169201 | intron-variant | UBE3B | GRCh38.p7 | 12:109484356 | GGCCTGCCCCATCCA[C/T]GGGGAGCAGCTACTA | 89910 |
rs11066855 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | UBE3B | GRCh38.p7 | 12:109484502 | gttcaagcagttctc[C/T]ggcctcagcctccct | 89910 |
rs11066856 | snp | C/G | 0.0577344 | 0.159793 | intron-variant | UBE3B | GRCh38.p7 | 12:109485333 | CAGGACGGGCAAGAT[C/G]TCTACGCTCATGGAG | 89910 |
rs11066912 | snp | C/T | 0.201418 | 0.245234 | intron-variant | UBE3B | GRCh38.p7 | 12:109493565 | CTTGTTAAGGCCAGG[C/T]TACTCTAAAGCCTTT | 89910 |
rs11066955 | snp | A/C | 0.114738 | 0.210248 | intron-variant | UBE3B | GRCh38.p7 | 12:109501028 | GTCATCTAGATTTGG[A/C]CCCCCACCACCTGCA | 89910 |
rs11067005 | snp | C/T | 0.0770498 | 0.180522 | intron-variant | UBE3B | GRCh38.p7 | 12:109511756 | TGGGAGCAAGGGCTT[C/T]CTGCAAAGCCACCGG | 89910 |
rs11067006 | snp | A/G | 0.118584 | 0.212673 | intron-variant | UBE3B | GRCh38.p7 | 12:109511837 | CATCTTGGCTGCAGC[A/G]TGGAGGGCTGGCTAG | 89910 |
rs11067030 | snp | C/T | 0.267364 | 0.249396 | intron-variant | UBE3B | GRCh38.p7 | 12:109517512 | TTGTTGGTACAAGAC[C/T]GTGCCTCCAATCTGC | 89910 |
rs11067032 | snp | C/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109517916 | TCACTCCTTACTGGA[C/G]AGCTTGTTTGAGTGC | 89910 |
rs11067039 | snp | G/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109519679 | TTATCTTAAATTTAG[G/T]CAGAATGGTTTAAAT | 89910 |
rs11067099 | snp | A/G | 0.115088 | 0.210473 | intron-variant | UBE3B | GRCh38.p7 | 12:109528683 | ACATGGTGAAACTCC[A/G]TCTCTACTAAAAATA | 89910 |
rs11067105 | snp | A/C/G | 0.00680556 | 0.0579372 | intron-variant | UBE3B | GRCh38.p7 | 12:109530086 | AAGTAAGAGGCGGGT[A/C/G]GGGGGAAGGGTGAAA | 89910 |
rs11067115 | snp | C/T | 0.240765 | 0.249829 | intron-variant | UBE3B | GRCh38.p7 | 12:109531881 | GCAGGTGCTGCCCCA[C/T]AAAACAGGTGTGTTT | 89910 |
rs11067150 | snp | A/C | 0.20111 | 0.245173 | intron-variant | UBE3B | GRCh38.p7 | 12:109539613 | GGGCTGAAAAGCCCC[A/C]GTCTGTGCCATCTAT | 89910 |
rs11067164 | snp | C/G | 0.115088 | 0.210473 | intron-variant | UBE3B | GRCh38.p7 | 12:109542149 | ATCTCATAGGGTGAG[C/G]GGGTGAAAAGGAGAA | 89910 |
rs11067165 | snp | A/G | 0.240765 | 0.249829 | intron-variant | UBE3B | GRCh38.p7 | 12:109542814 | ATTTCAGACTTAACA[A/G]CTTCTAGAATTGTGA | 89910 |
rs11442869 | in-del | -/A | 0.49941 | 0.0171624 | intron-variant | UBE3B | GRCh38.p7 | 12:109519889 | CCTAACCCCTGAATC[-/A]GGGGCACCATAGGAT | 89910 |
rs11453850 | in-del | -/T | 0.210615 | 0.246878 | intron-variant | UBE3B | GRCh38.p7 | 12:109513690 | CCACATTTTTTTTTT[-/T]CTTTTGGGAATTTTG | 89910 |
rs11548448 | snp | G/T | | | utr-variant-3-prime, intron-variant | UBE3B | GRCh38.p7 | 12:109536637 | GTTGTAGGATTTTTT[G/T]TTTTTGTAGCTAACT | 89910 |
rs11609388 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109528866 | aaaaaaaaaagaaaa[A/G]aaaaagaaaaggcca | 89910 |
rs11609630 | snp | C/T | 0.268452 | 0.249318 | intron-variant | UBE3B | GRCh38.p7 | 12:109481129 | AAAAAAAATGTCAAA[C/T]ATGGCCGGGCACAGT | 89910 |
rs11609871 | snp | C/G | 0.267091 | 0.249415 | intron-variant | UBE3B | GRCh38.p7 | 12:109527201 | GAGAGACTCTGAGGC[C/G]CAGCAACTATTGTCA | 89910 |
rs11609921 | snp | A/G | 0.268452 | 0.249318 | intron-variant | UBE3B | GRCh38.p7 | 12:109480600 | AAGCTGCAATGAACC[A/G]TGATTGCACCACTGC | 89910 |
rs11610418 | snp | C/T | 0.260504 | 0.249779 | intron-variant | UBE3B | GRCh38.p7 | 12:109528080 | GTCCTGCTGGGAAAC[C/T]TCCTATGTGGAAACT | 89910 |
rs11610558 | snp | C/T | 0.268995 | 0.249277 | intron-variant | UBE3B | GRCh38.p7 | 12:109488060 | TCTTAGTGCATCATA[C/T]GCATTAATCCATTTA | 89910 |
rs11611011 | snp | C/T | 0.268724 | 0.249298 | intron-variant | UBE3B | GRCh38.p7 | 12:109499143 | GAGGAGTTTCTGGTG[C/T]GAATGTTCACACGAG | 89910 |
rs11611012 | snp | A/G | 0.165853 | 0.235413 | intron-variant | UBE3B | GRCh38.p7 | 12:109507398 | CTGGCTCTTATCATT[A/G]TTACTCTCGTGGTGA | 89910 |
rs11611746 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109528867 | aaaaaaaaagaaaag[A/G]aaaagaaaaggccag | 89910 |
rs11611998 | snp | G/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109514394 | CGCTGAGGTTGCCCA[G/T]CCCTTGCAGCCTGGA | 89910 |
rs11614551 | snp | A/G | 0.270621 | 0.249148 | intron-variant | UBE3B | GRCh38.p7 | 12:109493825 | CATTCTCTTATCTCC[A/G]TTTTATTTATTTATT | 89910 |
rs11615336 | snp | A/C | 0.268452 | 0.249318 | upstream-variant-2KB, intron-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109476997 | TTCCTCACGCACACA[A/C]GTATCTACTCCGCAA | 89910 |
rs11829700 | snp | C/G | 0.209084 | 0.246629 | intron-variant | UBE3B | GRCh38.p7 | 12:109495179 | ATATTTTCAGCATTT[C/G]AGCTTCATAAAACAT | 89910 |
rs11830566 | snp | A/T | 0.209084 | 0.246629 | intron-variant | UBE3B | GRCh38.p7 | 12:109495175 | ACTGATATTTTCAGC[A/T]TTTCAGCTTCATAAA | 89910 |
rs11830623 | snp | C/T | 0.20111 | 0.245173 | intron-variant | UBE3B | GRCh38.p7 | 12:109481029 | agaatggcatgaacc[C/T]gggaggcggagcttg | 89910 |
rs12231062 | snp | C/T | 0.189261 | 0.242509 | intron-variant | UBE3B | GRCh38.p7 | 12:109516468 | aggcgtgagccccca[C/T]gcccagccTTGAGGA | 89910 |
rs12303137 | snp | C/G | 0.424007 | 0.179504 | intron-variant | UBE3B | GRCh38.p7 | 12:109533676 | GCAGGCAGCTGGACC[C/G]CTCAGAGCCAAGTGA | 89910 |
rs12306452 | snp | A/G | 0.239326 | 0.249772 | intron-variant | UBE3B | GRCh38.p7 | 12:109487917 | CCAGGTGGACCTGCT[A/G]TAGGGTCTGTGGGCC | 89910 |
rs12309013 | snp | A/G | 0.288127 | 0.247076 | intron-variant | UBE3B | GRCh38.p7 | 12:109539283 | CACAGCAGCCTAGGC[A/G]GCATTCATAGTTCTC | 89910 |
rs12314512 | snp | A/G | 0.0279526 | 0.114869 | intron-variant | UBE3B | GRCh38.p7 | 12:109511770 | TTCTGCAAAGCCACC[A/G]GAGGGCTGGAAGCTT | 89910 |
rs12317886 | snp | A/C | 0.0240643 | 0.107019 | intron-variant | UBE3B | GRCh38.p7 | 12:109516594 | ATTCCCACAAGTGTT[A/C]CAGGGAATGCTTCTG | 89910 |
rs12367550 | snp | A/G | 0.0988009 | 0.199095 | utr-variant-3-prime, intron-variant | UBE3B | GRCh38.p7 | 12:109535373 | GACGCTATGGACACC[A/G]TGAGTCCAAGGCGCT | 89910 |
rs12367754 | snp | A/G | 0.0752113 | 0.178743 | intron-variant | UBE3B | GRCh38.p7 | 12:109526096 | CCGAAATGCCAACAC[A/G]TTCCCCTCCATGACA | 89910 |
rs12423800 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBE3B | GRCh38.p7 | 12:109527207 | CTCTGAGGCCCAGCA[A/C]CTATTGTCACAGATA | 89910 |
rs12425082 | snp | G/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109540185 | ATGTGCAGGGTTTGG[G/T]TGGGGGAtttttggt | 89910 |
rs12425117 | snp | A/T | | | utr-variant-3-prime, intron-variant | UBE3B | GRCh38.p7 | 12:109535904 | CTTTAGCTCCAGGGA[A/T]CTGAGGCAGAGGCCC | 89910 |
rs12578737 | snp | A/G | 0.0285341 | 0.115986 | intron-variant, missense | UBE3B | GRCh38.p7 | 12:109534018 | AGCCTTCAGGGTTAC[A/G]GAGCTCTGTGTGTCT | 89910 |
rs12579621 | snp | C/G | 0 | 0 | intron-variant | UBE3B | GRCh38.p7 | 12:109491575 | ATTTGCCTTCACTTA[C/G]TTTGGAGATGTCAGG | 89910 |
rs12579916 | snp | G/T | 0.270892 | 0.249126 | intron-variant | UBE3B | GRCh38.p7 | 12:109486723 | GAGAGGAATTTTGAT[G/T]CTGTTATCAATATGA | 89910 |
rs12821045 | snp | A/G | 0.267091 | 0.249415 | intron-variant | UBE3B | GRCh38.p7 | 12:109541349 | CCTGTACTTGAGCTC[A/G]GATCACCACACCCAC | 89910 |
rs12822282 | snp | A/G | 0.268452 | 0.249318 | intron-variant | UBE3B | GRCh38.p7 | 12:109485402 | TGAACACATGATTAC[A/G]TAGATGAGGACAGAT | 89910 |
rs12826754 | snp | A/G | 0.268452 | 0.249318 | intron-variant | UBE3B | GRCh38.p7 | 12:109485439 | GAGGAGGTGAACCTC[A/G]TCTTACAGAGAAGGA | 89910 |
rs12831657 | snp | C/T | 0.164219 | 0.234823 | intron-variant | UBE3B | GRCh38.p7 | 12:109541462 | GCCTGCCATGAGGAT[C/T]AAACGAGGTCACATC | 89910 |
rs16940266 | snp | G/T | 0.0379877 | 0.132479 | intron-variant | UBE3B | GRCh38.p7 | 12:109493648 | CAGGACCTTTTAAAG[G/T]AAGATATCAGTGGTT | 89910 |
rs16940271 | snp | C/T | 0.0379877 | 0.132479 | intron-variant | UBE3B | GRCh38.p7 | 12:109497723 | AAATCCCACGCAGAA[C/T]AATTTCTAGGAATTT | 89910 |
rs16940277 | snp | C/T | 0.221439 | 0.248363 | intron-variant | UBE3B | GRCh38.p7 | 12:109505215 | TTATAGAAAATAACG[C/T]TTGTTTTTAAAATAC | 89910 |
rs16940335 | snp | C/T | 0.0130921 | 0.0798413 | utr-variant-3-prime, intron-variant | UBE3B | GRCh38.p7 | 12:109536295 | CTTTCTCCAAACGCT[C/T]GGTTCCTTTGAAGAT | 89910 |
rs17181453 | snp | A/G | 0.0685596 | 0.171987 | intron-variant | UBE3B | GRCh38.p7 | 12:109499287 | TAAAATGTAACACTA[A/G]CTAAATATCACCTAC | 89910 |
rs28384415 | snp | C/T | 0.00557542 | 0.0525036 | utr-variant-5-prime, splice-donor-variant, upstream-variant-2KB, nc-transcript-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109477765 | CTACCCGCAGGCCGA[C/T]CTTTATTCGCCGGAG | 89910 |
rs28384416 | snp | C/G | 0.0659589 | 0.169201 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109477378 | CGGGGCGGAAGTGGG[C/G]TGCGGACAGCGGAAG | 89910 |
rs33995372 | in-del | -/AAG | 0.442791 | 0.15916 | utr-variant-3-prime, cds-indel, intron-variant | UBE3B | GRCh38.p7 | 12:109536491 | ATGTGGATTTTTGAC[-/AAG]GAGGGGTAGTTTGTA | 89910 |
rs34011727 | in-del | -/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109500738 | CCTCATCTGAAACCT[-/G]GGGGATAATTTTCAC | 89910 |
rs34014477 | in-del | -/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109540576 | AAATCTGGTTTTTAT[-/G]GGGGCCATGGCAGTG | 89910 |
rs34032359 | in-del | -/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109504806 | TGGTTTGTGTCCAGC[-/T]TTTTTTTTTTTTTTT | 89910 |
rs34046186 | in-del | -/G | | | utr-variant-3-prime, intron-variant, downstream-variant-500B | UBE3B | GRCh38.p7 | 12:109534984 | CCAGGTGATGCCCAA[-/G]GCACAGGGCTGCAGA | 89910 |
rs34073495 | in-del | -/A | | | intron-variant | UBE3B | GRCh38.p7 | 12:109508526 | ATTCCACCTTTTCCC[-/A]AAAGGTTGGTGAAGA | 89910 |
rs34091986 | in-del | -/A/AAGATT/AAGATTC/AAGATTCA | | | intron-variant | UBE3B | GRCh38.p7 | 12:109519888 | GCCTAACCCCTGAAT[-/A/AAGATT/AAGATTC/AAGATTCA]CGGGGCACCATAGGA | 89910 |
rs34167074 | in-del | -/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109512383 | GAGTGCCACACACCC[-/G]GGGGATGAGAGAGAC | 89910 |
rs34194253 | snp | A/C | | | intron-variant | UBE3B | GRCh38.p7 | 12:109538057 | AAGGATGTCTTTATA[A/C]CCAGGAAAAATAAGT | 89910 |
rs34255116 | in-del | -/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109482707 | GTGCTGTGTGCTTTA[-/G]GCTGCTAGCAAAAGC | 89910 |
rs34306729 | snp | A/G | 0.276949 | 0.248543 | intron-variant | UBE3B | GRCh38.p7 | 12:109488402 | GCCACATTCCCTGTT[A/G]TTTAACTCCTGGAGT | 89910 |
rs34372859 | in-del | -/C | | | intron-variant | UBE3B | GRCh38.p7 | 12:109529335 | AAGTTGCTCTGACTT[-/C]CCCAGTTGAGTCCAC | 89910 |
rs34388733 | in-del | -/A | | | intron-variant | UBE3B | GRCh38.p7 | 12:109529790 | ATTTGTGTTTTTTGT[-/A]AAAATGGTTCAGAAA | 89910 |
rs34490570 | in-del | -/A | 0.49306 | 0.0584955 | intron-variant | UBE3B | GRCh38.p7 | 12:109492738 | GTGATACCTGGTCTC[-/A]AAAAAAAAAAAAAAA | 89910 |
rs34559049 | in-del | -/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109511422 | ATTCATTCAGCACAA[-/G]GGAAACGGTGGTTGC | 89910 |
rs34645364 | in-del | -/C | | | intron-variant | UBE3B | GRCh38.p7 | 12:109480089 | CTTAGTGCATTTAAG[-/C]ATAGGAAAAAAGTTA | 89910 |
rs34653918 | in-del | -/A | | | intron-variant | UBE3B | GRCh38.p7 | 12:109481314 | GAGTGAGACTATCTC[-/A]AAAAAAAAAAAAAGG | 89910 |
rs34662493 | snp | A/G | 0.0524604 | 0.153226 | intron-variant | UBE3B | GRCh38.p7 | 12:109509389 | TTAAGCTCTACATGC[A/G]TTAGGTATTTGTCCT | 89910 |
rs34766258 | in-del | -/G | | | intron-variant, downstream-variant-500B | UBE3B | GRCh38.p7 | 12:109536976 | CTGTCACCATAGGTT[-/G]GGGTGTATATCTTTG | 89910 |
rs34784335 | in-del | -/C | | | intron-variant | UBE3B | GRCh38.p7 | 12:109514854 | AGATCTGTCAACCAG[-/C]CTCAGCAAGATGCTT | 89910 |
rs34785014 | snp | C/T | 0.195837 | 0.244062 | intron-variant | UBE3B | GRCh38.p7 | 12:109539548 | TCCTCTTCCATGAAA[C/T]GAGGATAGCAGCACC | 89910 |
rs34849121 | in-del | -/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109526144 | AATGTTTGAACAAGG[-/G]ATTGGGTGAGAAAAA | 89910 |
rs34898874 | in-del | -/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109480776 | GCTTCACCATGTGCA[-/T]TGCTGTGGAAAATTT | 89910 |
rs34980590 | in-del | -/T | 0.339656 | 0.233371 | intron-variant | UBE3B | GRCh38.p7 | 12:109504807 | TGGTTTGTGTCCAGC[-/T]TTTTTTTTTTTTTTC | 89910 |
rs34998702 | in-del | -/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109512144 | TGGCATTCAGGAGGG[-/T]AGGAGCTTGTGTGGG | 89910 |
rs35245384 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant, utr-variant-3-prime | UBE3B | GRCh38.p7 | 12:109534173 | AGCTACACAGTCCTC[A/G]GCCTCCATGCTTAAG | 89910 |
rs35317381 | in-del | -/A | 0.271702 | 0.249056 | intron-variant | UBE3B | GRCh38.p7 | 12:109480650 | GCGAGACCCTGCCTT[-/A]AAAAAAAAAAAAAAG | 89910 |
rs35378454 | in-del | -/C | | | intron-variant | UBE3B | GRCh38.p7 | 12:109511089 | TGTTCCCATCAGACT[-/C]CTTGAGAAACAGACA | 89910 |
rs35430779 | in-del | -/C | | | upstream-variant-2KB, intron-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109476647 | GCCCCTGGCATCTCT[-/C]CCCCAGGATTCCAAG | 89910 |
rs35478809 | in-del | -/A | | | intron-variant | UBE3B | GRCh38.p7 | 12:109539399 | CCAGAGCCCCAGCTG[-/A]AGTGCAGATCTTACG | 89910 |
rs35522205 | in-del | -/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109519040 | TCTATTAGGCTTCCA[-/G]GATATTAAAGTCCTG | 89910 |
rs35545972 | in-del | -/C | | | intron-variant | UBE3B | GRCh38.p7 | 12:109524624 | CTGGTCCCTTGTCCT[-/C]CCCCACCCCTCGCCC | 89910 |
rs35575861 | in-del | -/A | | | intron-variant | UBE3B | GRCh38.p7 | 12:109510270 | TGATGACAACTGCGG[-/A]AGACAAGAGCTGTCC | 89910 |
rs35613116 | snp | A/C | 0.111576 | 0.20818 | intron-variant | UBE3B | GRCh38.p7 | 12:109500271 | ATTATGAACTTAAAA[A/C]CATGAGAAACACTAG | 89910 |
rs35691047 | snp | C/T | 0.268452 | 0.249318 | intron-variant | UBE3B | GRCh38.p7 | 12:109494780 | AAAGATCACACCCCT[C/T]CAAACATTGAGGCAG | 89910 |
rs35710991 | in-del | -/C | | | frameshift-variant | UBE3B | GRCh38.p7 | 12:109543605 | CACTTTCGGAGGCAG[-/C]ATGGATGACTTGAAG | 89910 |
rs35754246 | in-del | -/T | 0.268452 | 0.249318 | intron-variant | UBE3B | GRCh38.p7 | 12:109482702 | GTCAGTGCTGTGTGC[-/T]TTTAGGCTGCTAGCA | 89910 |
rs35787958 | in-del | -/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109518311 | ACTCAGCTCCTCCAG[-/T]ACCTGCCATGTGACG | 89910 |
rs35814460 | in-del | -/C | | | intron-variant | UBE3B | GRCh38.p7 | 12:109512140 | GGTCTGGCATTCAGG[-/C]AGGGAGGAGCTTGTG | 89910 |
rs35857041 | in-del | -/G | | | utr-variant-3-prime, intron-variant, downstream-variant-500B | UBE3B | GRCh38.p7 | 12:109535102 | GTCTGTCTTTCCTTA[-/G]CCGTCTGAGTGAGCT | 89910 |
rs35900683 | in-del | -/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109522978 | GCCTGGGCCACCTGG[-/G]AAAGCATGGCCTCCT | 89910 |
rs35903978 | in-del | -/A/AA/AAA | 0.25634 | 0.24992 | intron-variant | UBE3B | GRCh38.p7 | 12:109526870 | GTGAGACTCCGTCTC[-/A/AA/AAA]AAAAAAAAAAAAAAA | 89910 |
rs35964882 | in-del | -/TT | 0.5 | 0 | intron-variant | UBE3B | GRCh38.p7 | 12:109520744 | GTTCTGTAGGTTTGA[-/TT]TTTTTTTTTTTTCTT | 89910 |
rs35973716 | in-del | -/T | | | intron-variant, frameshift-variant | UBE3B | GRCh38.p7 | 12:109533983 | TGCTTCATTTCCTCA[-/T]TTGGCCAAAGGAGAA | 89910 |
rs36081816 | in-del | -/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109482733 | AAAGCTGTTCCTTTA[-/G]GAAAAAACAGTTACT | 89910 |
rs41444250 | snp | C/T | 0.0360663 | 0.129354 | intron-variant | UBE3B | GRCh38.p7 | 12:109486974 | TTACTCTAGCTGCCA[C/T]GTTACTGAATATATT | 89910 |
rs55735873 | snp | C/T | 0.0562307 | 0.157967 | intron-variant | UBE3B | GRCh38.p7 | 12:109500846 | CGTACTCAGGGGTGG[C/T]GGCTATTAACAATAT | 89910 |
rs55815037 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | UBE3B | GRCh38.p7 | 12:109537588 | TCACAAGGAGCGTTC[A/G]TGTAACTAAAAGAAA | 89910 |
rs55828308 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109541417 | GGAGATTCATTTTCC[C/T]CAGCTGTAAAGTAGT | 89910 |
rs55911244 | snp | A/G | 0.0329836 | 0.124112 | intron-variant | UBE3B | GRCh38.p7 | 12:109537395 | TCTGTCCTGACCCTC[A/G]GCAGCTCTGAAGTCC | 89910 |
rs55916382 | snp | C/T | | | downstream-variant-500B | UBE3B | GRCh38.p7 | 12:109544040 | GGGTTGAGCCTCAGA[C/T]TGCAGGGTGTGTTTG | 89910 |
rs55923636 | in-del | -/TA | | | intron-variant | UBE3B | GRCh38.p7 | 12:109526884 | CAAAAAAAAAAAAAA[-/TA]ATTGATTTGCAAAAT | 89910 |
rs55980475 | snp | A/T | 0.0722614 | 0.17581 | intron-variant | UBE3B | GRCh38.p7 | 12:109526664 | GATCACGAGGTCAGG[A/T]GTTCGAGACCAGCCT | 89910 |
rs56007067 | snp | A/T | 0.00755907 | 0.0610114 | intron-variant | UBE3B | GRCh38.p7 | 12:109485070 | TCTAATTTGTAAATC[A/T]TGGCAATTAATTTGA | 89910 |
rs56143656 | snp | G/T | 0.115088 | 0.210473 | intron-variant | UBE3B | GRCh38.p7 | 12:109515367 | TATTACTGTTTTTTT[G/T]TTGTTGTTGTTGTTG | 89910 |
rs56244055 | snp | A/G | 0.270621 | 0.249148 | intron-variant | UBE3B | GRCh38.p7 | 12:109498406 | CATCAGGGAAAGCCC[A/G]AGTGTTTTGCCTGTC | 89910 |
rs56259345 | snp | G/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109479920 | TTCCATGGACCCTCT[G/T]CCATTGAGGCACTGT | 89910 |
rs56330650 | snp | C/T | 0.0722614 | 0.17581 | intron-variant | UBE3B | GRCh38.p7 | 12:109523317 | TTCCTCTCGCCAGCC[C/T]ATTCCCCACATAAAA | 89910 |
rs56372973 | snp | G/T | 0.0566069 | 0.158427 | intron-variant | UBE3B | GRCh38.p7 | 12:109515370 | TACTGTTTTTTTGTT[G/T]TTGTTGTTGTTGTTT | 89910 |
rs57284418 | snp | C/T | 0.039522 | 0.134904 | intron-variant | UBE3B | GRCh38.p7 | 12:109488491 | CAGGCTGAGTGCCCA[C/T]AGAGCAGTTGTAAAG | 89910 |
rs57392705 | snp | G/T | 0.0629771 | 0.165899 | downstream-variant-500B | UBE3B | GRCh38.p7 | 12:109543891 | CCAGAGATGGTACCA[G/T]AAGGAGGGTTGGAGC | 89910 |
rs57447325 | snp | C/T | | | downstream-variant-500B | UBE3B | GRCh38.p7 | 12:109543911 | AGGGTTGGAGCGGGC[C/T]TCTCAAAGCAAGCCT | 89910 |
rs57481695 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109516334 | ATGCCACCACACCCA[A/G]CTAATTTTTGTATTT | 89910 |
rs58979120 | in-del | -/A | | | intron-variant | UBE3B | GRCh38.p7 | 12:109503496 | GGTTGCAAAAAAAAA[-/A]GGAAAAAGAAAACCA | 89910 |
rs59084691 | in-del | -/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109516189 | TTTTTTTTTTTTTTT[-/T]GAGACAGAGTCTCAC | 89910 |
rs59505191 | snp | A/G | 0.209084 | 0.246629 | intron-variant | UBE3B | GRCh38.p7 | 12:109495717 | GGAAACAAAGGGATG[A/G]GCCGAAATAAAGGGA | 89910 |
rs59832747 | snp | A/G | 0.0287284 | 0.116357 | intron-variant | UBE3B | GRCh38.p7 | 12:109526730 | ACAAAAATTAGCTGG[A/G]CGTGGTGGCTCATGC | 89910 |
rs59975102 | snp | A/G | 0.0486741 | 0.148216 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109477688 | TGCCCCGGGTCTGGC[A/G]GAACTCGGGTGTTTT | 89910 |
rs60108170 | in-del | -/T | 0.0271762 | 0.113356 | intron-variant, upstream-variant-2KB | UBE3B, KCTD10 | GRCh38.p7 | 12:109479278 | TACAATAAAGCTCAC[-/T]TACATGCTACATGCT | 89910 |
rs60123067 | snp | C/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109516228 | CCAGGCTGGAGTGCA[C/G]TGGCACGATCTTGGC | 89910 |
rs60197450 | snp | A/G | 0.0329836 | 0.124112 | intron-variant | UBE3B | GRCh38.p7 | 12:109537241 | TTCTGGGTGTGCCAG[A/G]CGTTGTTCCCTTAGT | 89910 |
rs60352001 | in-del | -/TTTTTG | | | intron-variant | UBE3B | GRCh38.p7 | 12:109506365 | TTGTTTTTGTTTTTG[-/TTTTTG]GAGACAGAGTTTCGC | 89910 |
rs60434971 | snp | G/T | 0.0189856 | 0.0955633 | intron-variant | UBE3B | GRCh38.p7 | 12:109524925 | GGAGCAGAGACCCTG[G/T]TCTCAGGGCCGCAGC | 89910 |
rs60733743 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | UBE3B | GRCh38.p7 | 12:109482683 | CAATATGGGAGCCTC[C/T]GGGGGTCAGTGCTGT | 89910 |
rs61082692 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | UBE3B | GRCh38.p7 | 12:109530411 | ATTGAGGCATGAACT[A/T]CTGGCTTTAAGAGAA | 89910 |
rs61551572 | snp | C/T | 0.0256215 | 0.110247 | intron-variant | UBE3B | GRCh38.p7 | 12:109501244 | TATTTTTGTAATCTT[C/T]TTTGCCATGTTGAGT | 89910 |
rs61733773 | snp | C/T | 0.00918329 | 0.0671365 | synonymous-codon, intron-variant | UBE3B | GRCh38.p7 | 12:109530040 | GCGTCTCATCTCTGG[C/T]GACAATGCTGAGATT | 89910 |
rs61739704 | snp | C/G/T | 0.00376588 | 0.0432297 | synonymous-codon, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109501437 | GGTGCCTCTGATCCG[C/G/T]ATCTTCTTCTGTGAC | 89910 |
rs61739922 | snp | A/G | 0.000181203 | 0.00951675 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109488646 | CACAGACACTTCAAC[A/G]TGGAAAATTCTTCGG | 89910 |
rs61744923 | snp | A/G/T | 0.00118641 | 0.0243271 | missense, intron-variant | UBE3B | GRCh38.p7 | 12:109530644 | ACACCGGATGAGAGA[A/G/T]CTATGTTTCTGAAGG | 89910 |
rs61744991 | snp | C/T | 0.00145001 | 0.0268869 | synonymous-codon, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109521150 | CTGCTCTTGGCAGGA[C/T]GGCTACGAGCAGCTT | 89910 |
rs61748069 | snp | C/T | 0.0481996 | 0.147569 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109498251 | CTCACTGTTTTAGAA[C/T]CCCATGACATGCTTC | 89910 |
rs61748816 | snp | A/G | 0.000263583 | 0.011477 | missense, intron-variant | UBE3B | GRCh38.p7 | 12:109530623 | GATATTCTGGCCTCC[A/G]ACTTCACACCGGATG | 89910 |
rs61760194 | snp | C/T | 0.0176436 | 0.0922524 | synonymous-codon, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109510408 | GCTTATGGTGCTGTA[C/T]GAGCGGGACTGCCGG | 89910 |
rs61941589 | snp | C/T | 0.20111 | 0.245173 | upstream-variant-2KB, intron-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109477051 | CTAACCGCCAGGGAG[C/T]CTCCCTACCACCACC | 89910 |
rs61941590 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109481329 | AAAAAAAAAAAAAAG[A/G]AAAATGTCAAATATA | 89910 |
rs61941591 | snp | A/C | 0.268452 | 0.249318 | intron-variant | UBE3B | GRCh38.p7 | 12:109482160 | GGAGATAATACTATT[A/C]AGTCCAATGTTTATT | 89910 |
rs61941592 | snp | A/G | 0.27278 | 0.24896 | intron-variant | UBE3B | GRCh38.p7 | 12:109492692 | AGGCTGCAGCGAGCC[A/G]TGATTGAGCTTCTCC | 89910 |
rs61941630 | snp | C/T | 0.5 | 0 | intron-variant | UBE3B | GRCh38.p7 | 12:109496969 | TGCCTAACCTGAAAT[C/T]TCAAAGCTTTACTCC | 89910 |
rs61941631 | snp | C/T | 0.270621 | 0.249148 | intron-variant | UBE3B | GRCh38.p7 | 12:109497670 | ACTTGTCCATTTCCC[C/T]AGTGTATGTCCCCAA | 89910 |
rs61941633 | snp | C/T | 0.0659589 | 0.169201 | intron-variant | UBE3B | GRCh38.p7 | 12:109505335 | CATTGCTCTGCCAGG[C/T]CCAGTGTCTCCATCT | 89910 |
rs61941634 | snp | C/T | 0.0644693 | 0.167566 | intron-variant | UBE3B | GRCh38.p7 | 12:109509429 | CCTCCCCTTTCCCCC[C/T]ACCCCTGATGATATC | 89910 |
rs61941635 | snp | A/G | 0.0644693 | 0.167566 | intron-variant | UBE3B | GRCh38.p7 | 12:109516446 | CCTCCCAGAGTGCTG[A/G]GATTACAGGCGTGAG | 89910 |
rs61941636 | snp | A/G | 0.186421 | 0.24178 | intron-variant | UBE3B | GRCh38.p7 | 12:109525171 | ATATCCATTTGCCAG[A/G]TGCGAGTCCTGGATG | 89910 |
rs61999293 | snp | C/T | 0.000801715 | 0.0200054 | synonymous-codon, utr-variant-3-prime, intron-variant, downstream-variant-500B | UBE3B | GRCh38.p7 | 12:109534731 | GAAGAGCGTCCTCCG[C/T]GAGAAGCTGCGCTAC | 89910 |
rs66778424 | multinucleotide-polymorphism | AT/TC | 0.5 | 0 | intron-variant | UBE3B | GRCh38.p7 | 12:109503646 | CATGTCACAAATTCT[AT/TC]GAAAACCTTATCTTT | 89910 |
rs67183322 | multinucleotide-polymorphism | CAA/GAG | 0.5 | 0 | utr-variant-3-prime, intron-variant | UBE3B | GRCh38.p7 | 12:109536176 | CAGGCTTCTGGAAAA[CAA/GAG]TGTGTGCTCTACTTT | 89910 |
rs67731731 | in-del | -/A | 0.275672 | 0.248678 | intron-variant | UBE3B | GRCh38.p7 | 12:109521585 | AGAGAAATGTAAAAT[-/A]AAATGTTAACGGTAC | 89910 |
rs71079571 | in-del | -/C | 0 | 0 | intron-variant | UBE3B | GRCh38.p7 | 12:109523685 | CTGGTGCTGCCCCCC[-/C]ACTGACAGGTGAGAC | 89910 |
rs71297464 | in-del | AAGATTCA/C | 0.5 | 0 | intron-variant | UBE3B | GRCh38.p7 | 12:109519889 | GCCTAACCCCTGAAT[AAGATTCA/C]GGGGCACCATAGGAT | 89910 |
rs71443861 | in-del | -/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109516168 | TTTTTCTTTTTTTTC[-/T]TTTTTTTTTTTTTTT | 89910 |
rs71456694 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | UBE3B | GRCh38.p7 | 12:109500512 | TTGTACCTGAGTGAC[A/G]TCCCTGGGTCCTATC | 89910 |
rs72175145 | in-del | -/AG | 0.281049 | 0.248064 | intron-variant | UBE3B | GRCh38.p7 | 12:109527735 | GGCCCAGCCAGGGCC[-/AG]AGAGAGAGCATGGTG | 89910 |
rs73196264 | snp | A/G | 0.0429648 | 0.14013 | intron-variant | UBE3B | GRCh38.p7 | 12:109480776 | TGCTTCACCATGTGC[A/G]TGCTGTGGAAAATTT | 89910 |
rs73196268 | snp | A/C | 0.113955 | 0.209749 | intron-variant | UBE3B | GRCh38.p7 | 12:109490022 | CTGTGACTCCTGCCC[A/C]CCAGTGTGCAACTTC | 89910 |
rs73196270 | snp | C/T | 0.0517044 | 0.152246 | intron-variant | UBE3B | GRCh38.p7 | 12:109493854 | TTTGTGAGACAAGGT[C/T]GTGCTTTGCCATCAA | 89910 |
rs73196271 | snp | C/G | 0.0554779 | 0.157039 | intron-variant | UBE3B | GRCh38.p7 | 12:109496183 | TGTGGTCTTTTGCTA[C/G]TGGCTTTTTTCACTT | 89910 |
rs73196272 | snp | C/T | 0.0524604 | 0.153226 | intron-variant | UBE3B | GRCh38.p7 | 12:109496324 | ACTTTTTGGCTATTA[C/T]AAATAGTGCTGCTGT | 89910 |
rs73196275 | snp | G/T | 0.0517044 | 0.152246 | intron-variant | UBE3B | GRCh38.p7 | 12:109498433 | TGTCACTATTCTAGA[G/T]ATTTGGTTGTTTTCT | 89910 |
rs73196278 | snp | A/G | 0.0517044 | 0.152246 | intron-variant | UBE3B | GRCh38.p7 | 12:109506881 | AGCAGCCTAGCTTCA[A/G]TCAATCACAGGTGGC | 89910 |
rs73196280 | snp | A/G | 0.0520825 | 0.152737 | intron-variant | UBE3B | GRCh38.p7 | 12:109511643 | GCTTTTGGAGAGTCA[A/G]ATGTGCAGTGTGGCT | 89910 |
rs73196282 | snp | A/G | 0.0486741 | 0.148216 | intron-variant | UBE3B | GRCh38.p7 | 12:109519327 | ACATTCACCTCCCAA[A/G]AGGCATGGATATAAT | 89910 |
rs73196283 | snp | C/G/T | 0.0197687 | 0.0974348 | intron-variant | UBE3B | GRCh38.p7 | 12:109519881 | ACTTTGAAGCCTAAC[C/G/T]CCTGAATCGGGGCAC | 89910 |
rs73196284 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109520758 | ATTTTTTTTTTTTTT[C/T]TTTTTTCTTTTTTTT | 89910 |
rs73196285 | snp | C/T | 0.0558544 | 0.157504 | intron-variant | UBE3B | GRCh38.p7 | 12:109523539 | GCTGGCTTTTCCTCC[C/T]GGAAGCTCCCCAACT | 89910 |
rs73196288 | snp | A/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109526883 | CTCAAAAAAAAAAAA[A/T]AATTGATTTGCAAAA | 89910 |
rs73196292 | snp | C/T | 0.0517044 | 0.152246 | intron-variant | UBE3B | GRCh38.p7 | 12:109529607 | TCTCCTTGTGATTCC[C/T]GACATAGTGGGGGCT | 89910 |
rs73196293 | snp | A/G | 0.0524604 | 0.153226 | intron-variant | UBE3B | GRCh38.p7 | 12:109531457 | CTTGACAGAATATCA[A/G]TGAACATTTTGCCAT | 89910 |
rs73196294 | snp | A/G | 0.0532157 | 0.154195 | intron-variant | UBE3B | GRCh38.p7 | 12:109532165 | GGGCAGACCTGAGCC[A/G]GCCTAAATTGGGATG | 89910 |
rs73196297 | snp | G/T | 0.0520825 | 0.152737 | utr-variant-3-prime, intron-variant | UBE3B | GRCh38.p7 | 12:109535487 | CCCGGACCTATTCCC[G/T]TCCTATGCATTCACA | 89910 |
rs73198406 | snp | C/T | 0.0517044 | 0.152246 | intron-variant | UBE3B | GRCh38.p7 | 12:109541442 | AGTAGTGAATAACAG[C/T]TCCTGCCTGCCATGA | 89910 |
rs73198407 | snp | G/T | 0.0517044 | 0.152246 | intron-variant | UBE3B | GRCh38.p7 | 12:109541993 | CCAAAAAAGGTCCCA[G/T]GCACAGGTTCTGGGG | 89910 |
rs73407594 | snp | C/T | 0.199564 | 0.24486 | intron-variant | UBE3B | GRCh38.p7 | 12:109501614 | CCTATATGGATGTTC[C/T]GCTGTGTTTGTGGGA | 89910 |
rs73414033 | snp | A/C | 0.0486741 | 0.148216 | intron-variant | UBE3B | GRCh38.p7 | 12:109514086 | CATTTGTTAAAGCCT[A/C]AGCTCTGCCTGGCTC | 89910 |
rs73414043 | snp | G/T | 0.110167 | 0.207236 | intron-variant | UBE3B | GRCh38.p7 | 12:109532695 | AACGCAGGGGCTGCC[G/T]CTTGGAGAACGCCGG | 89910 |
rs73414054 | snp | A/G | 0.0486741 | 0.148216 | intron-variant | UBE3B | GRCh38.p7 | 12:109539742 | GACGCTTTGGCTGAC[A/G]TTAACAGGACATCCC | 89910 |
rs74501991 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109490414 | AATTGTTGAGAAAGC[C/T]TGATTGCTGTTTAAA | 89910 |
rs74507313 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | UBE3B | GRCh38.p7 | 12:109525720 | GACATAATTTTTCTC[C/T]CGACTATAAAGATAA | 89910 |
rs74649352 | snp | A/G | | | intron-variant, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109508637 | GCAGATTGGGTGAGG[A/G]TCATGGAAGAACTCA | 89910 |
rs74679026 | snp | C/G | 0.0162398 | 0.0886349 | intron-variant | UBE3B | GRCh38.p7 | 12:109507025 | GAGCTGTCTGAACCT[C/G]GTCTGGTTCTGAGGG | 89910 |
rs74719685 | snp | C/T | 0.0179497 | 0.0930197 | intron-variant | UBE3B | GRCh38.p7 | 12:109490150 | GCTGTCCTCTTCTTC[C/T]TTCCCCTGCCTTGTC | 89910 |
rs74820297 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | UBE3B | GRCh38.p7 | 12:109540804 | GTTATTTTACAACAA[C/G]AACATTGTAGCCAGA | 89910 |
rs74838860 | snp | A/C | 0.0452528 | 0.143452 | utr-variant-3-prime, intron-variant | UBE3B | GRCh38.p7 | 12:109535869 | TCCTCTGCCCTCATT[A/C]TTTACCTTTGTTGTA | 89910 |
rs74873251 | snp | A/T | 0.0689305 | 0.172377 | intron-variant | UBE3B | GRCh38.p7 | 12:109500660 | AGCACCTCCGCAGAC[A/T]GCCTGCTCTCCGCTC | 89910 |
rs74885174 | snp | G/T | | | intron-variant, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109508636 | GGCAGATTGGGTGAG[G/T]ATCATGGAAGAACTC | 89910 |
rs74961634 | snp | A/T | 0.0726307 | 0.176182 | intron-variant | UBE3B | GRCh38.p7 | 12:109507413 | GTTACTCTCGTGGTG[A/T]TAATGCTTTTCTCCA | 89910 |
rs74978040 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | UBE3B | GRCh38.p7 | 12:109496581 | TATTTAGCCATCCCA[A/G]TGGCTGTACAGGGGT | 89910 |
rs75238516 | snp | A/G | 0.00478085 | 0.0486577 | utr-variant-3-prime, intron-variant | UBE3B | GRCh38.p7 | 12:109536583 | CCTTTTGTAACTGGT[A/G]TTCACTGACACCTTG | 89910 |
rs75248373 | snp | C/G | 0.0792508 | 0.182605 | intron-variant | UBE3B | GRCh38.p7 | 12:109499438 | TGTCTGTGGCATAGC[C/G]AGGATTTGAAGTCAG | 89910 |
rs75255116 | in-del | -/GCT | | | intron-variant | UBE3B | GRCh38.p7 | 12:109543012 | GAACCGGCAGCTGCT[-/GCT]CAGCCCCAGCAGCTG | 89910 |
rs75316127 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBE3B | GRCh38.p7 | 12:109514102 | AGCTCTGCCTGGCTC[A/G]CGTGCACAGCACTTC | 89910 |
rs75411486 | snp | A/G | 0.0252325 | 0.109451 | intron-variant | UBE3B | GRCh38.p7 | 12:109519220 | TGGATATCAGTGATA[A/G]AGCTGGGCCTGGAAG | 89910 |
rs75507630 | snp | A/G | 0.0681886 | 0.171594 | intron-variant | UBE3B | GRCh38.p7 | 12:109537485 | GGCTTGTTAGGATCC[A/G]GTCAGGAAAGAACCC | 89910 |
rs75524776 | snp | A/G | 0.0558544 | 0.157504 | intron-variant | UBE3B | GRCh38.p7 | 12:109538471 | GCAGCCTCCCTGTGT[A/G]TTCCTTATCTAGAAC | 89910 |
rs75533804 | snp | A/G | 0.0267878 | 0.112589 | intron-variant | UBE3B | GRCh38.p7 | 12:109481804 | CAGAAGATGGCTACC[A/G]TTTCTCTCCAAGCCT | 89910 |
rs75598829 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | UBE3B | GRCh38.p7 | 12:109537366 | CTGCCAGGTGTTTGC[C/T]CCGCCTTGGTGCTTC | 89910 |
rs75632822 | snp | C/G | 0.109814 | 0.206997 | intron-variant | UBE3B | GRCh38.p7 | 12:109538452 | TTCCTGCCCCACGTG[C/G]AGGGCAGCCTCCCTG | 89910 |
rs75845591 | snp | A/G | 0.0364509 | 0.129988 | intron-variant | UBE3B | GRCh38.p7 | 12:109541657 | AAATCACAACAAGCC[A/G]GGTGGCTTAAAACAA | 89910 |
rs75866186 | snp | A/G | 0.0185938 | 0.0946107 | utr-variant-3-prime, intron-variant | UBE3B | GRCh38.p7 | 12:109535925 | GCAGAGGCCCTGTTT[A/G]TGGTCTGTGTTGACA | 89910 |
rs75897202 | snp | G/T | 0.5 | 0 | intron-variant | UBE3B | GRCh38.p7 | 12:109516190 | TTTTTTTTTTTTTTT[G/T]AGACAGAGTCTCACT | 89910 |
rs75953308 | snp | C/G | 0.0726307 | 0.176182 | intron-variant | UBE3B | GRCh38.p7 | 12:109482473 | TTAGGATAGATGGCC[C/G]CTAGTTCTAGCCATC | 89910 |
rs75979357 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | UBE3B | GRCh38.p7 | 12:109494643 | AAATGCAACAGCTAC[A/G]GGTAGGCTAAAGAAA | 89910 |
rs76062639 | snp | A/C | 0.0629771 | 0.165899 | intron-variant | UBE3B | GRCh38.p7 | 12:109492013 | AGCATGGGTTGGCCA[A/C]ATTTTCTGGAAAGAG | 89910 |
rs76192900 | snp | C/G | 0.0310518 | 0.120672 | intron-variant | UBE3B | GRCh38.p7 | 12:109491700 | ACATGTTTAAACTGT[C/G]AAGGGGAACACTAGC | 89910 |
rs76251788 | snp | C/T | 0.0689305 | 0.172377 | intron-variant | UBE3B | GRCh38.p7 | 12:109539478 | AAACCCCAGCTCTGC[C/T]GCCCACGATCTGGGA | 89910 |
rs76334512 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | UBE3B | GRCh38.p7 | 12:109521070 | TGCTGGGAGAGCTTC[A/G]CACAGAGGAGAGGGA | 89910 |
rs76402972 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | UBE3B | GRCh38.p7 | 12:109538487 | TTCCTTATCTAGAAC[A/G]CAGGAATCTTGATGT | 89910 |
rs76462278 | snp | A/G | 0.5 | 0 | intron-variant, downstream-variant-500B | UBE3B | GRCh38.p7 | 12:109537174 | TTTCAAAAGTGATCA[A/G]CGGATGTTGAACAAA | 89910 |
rs76575777 | snp | A/G | 0.0696718 | 0.173152 | intron-variant | UBE3B | GRCh38.p7 | 12:109527852 | GTGTCAGGCTCAGAG[A/G]AGGGCTTAAATGACA | 89910 |
rs76600751 | snp | G/T | 0.5 | 0 | intron-variant, utr-variant-5-prime, downstream-variant-500B | UBE3B | GRCh38.p7 | 12:109490977 | CTCAGTTTACTTTTT[G/T]GCTCTTTTATGTACA | 89910 |
rs76708701 | snp | C/T | 0.0329836 | 0.124112 | intron-variant | UBE3B | GRCh38.p7 | 12:109483188 | CTTTGACCTATAGGA[C/T]ACCTGGTTTGAATTA | 89910 |
rs76720290 | snp | C/G | 0.5 | 0 | intron-variant, utr-variant-5-prime, downstream-variant-500B | UBE3B | GRCh38.p7 | 12:109490978 | TCAGTTTACTTTTTT[C/G]CTCTTTTATGTACAA | 89910 |
rs76915832 | snp | A/G | 0.029116 | 0.117091 | intron-variant | UBE3B | GRCh38.p7 | 12:109531473 | TGAACATTTTGCCAT[A/G]TTCTGGTGGTAAATT | 89910 |
rs76949522 | snp | C/T | 0.0271762 | 0.113356 | upstream-variant-2KB, intron-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109475820 | TACATTTCAACTAAA[C/T]TAAGTCACATAATTG | 89910 |
rs77075866 | snp | G/T | 0.5 | 0 | intron-variant | UBE3B | GRCh38.p7 | 12:109498842 | TTGTTTTTTTTTTTT[G/T]GAAGACAGGGTCTCA | 89910 |
rs77263283 | in-del | -/TG | | | upstream-variant-2KB, intron-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109475887 | ACCGCCAATTGCAAC[-/TG]TTCCATCAAATGACA | 89910 |
rs77555099 | in-del | -/GT/TG | | | upstream-variant-2KB, intron-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109475888 | CCGCCAATTGCAACT[-/GT/TG]TCCATCAAATGACAT | 89910 |
rs77622943 | in-del | -/TAAT | | | intron-variant, upstream-variant-2KB | KCTD10, UBE3B | GRCh38.p7 | 12:109475539 | ACACCCCAGATCAAT[-/TAAT]CAGTATCTCAGAGAT | 89910 |
rs77687467 | snp | G/T | 0.0228947 | 0.104514 | intron-variant | UBE3B | GRCh38.p7 | 12:109498449 | ATTTGGTTGTTTTCT[G/T]TAACAATTGGAAGTG | 89910 |
rs77708954 | snp | A/G | 0.5 | 0 | intron-variant | UBE3B | GRCh38.p7 | 12:109481327 | TCAAAAAAAAAAAAA[A/G]GGAAAATGTCAAATA | 89910 |
rs77728485 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | UBE3B | GRCh38.p7 | 12:109502762 | GATTTCCAGTATAAG[A/G]ATCCCATGTAAGATT | 89910 |
rs77729521 | snp | A/G | 0.0267878 | 0.112589 | intron-variant | UBE3B | GRCh38.p7 | 12:109543281 | GGTGGAGCTGGACAA[A/G]ATGATGTTCACTGGA | 89910 |
rs77764526 | snp | C/T | 0.0410537 | 0.137264 | intron-variant | UBE3B | GRCh38.p7 | 12:109509482 | TACAGTAAGTATCTC[C/T]ACAAGATAAAGCTTA | 89910 |
rs77764714 | snp | A/C | 0.5 | 0 | intron-variant | UBE3B | GRCh38.p7 | 12:109481314 | GAGTGAGACTATCTC[A/C]AAAAAAAAAAAAAGG | 89910 |
rs77876679 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | UBE3B | GRCh38.p7 | 12:109509453 | TGATATCATATCATT[C/T]TATCTGTAGATTTTA | 89910 |
rs77891045 | snp | A/G | 0.0314385 | 0.121371 | intron-variant | UBE3B | GRCh38.p7 | 12:109522584 | CAGGAACCTGGAGAA[A/G]CCAGATGCTTTCCAA | 89910 |
rs77952639 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | UBE3B | GRCh38.p7 | 12:109503700 | CATGGATATGCCCAA[C/T]ATTTTCCTTTTTAGC | 89910 |
rs77985171 | snp | A/T | 0.0130921 | 0.0798413 | intron-variant | UBE3B | GRCh38.p7 | 12:109519197 | AGAGAACTTCAGTCA[A/T]GGTCACTTGGATATC | 89910 |
rs78066786 | snp | A/G | 0.0310518 | 0.120672 | intron-variant | UBE3B | GRCh38.p7 | 12:109499359 | TGGAGAGTAGGGATC[A/G]TCATTCCAATCTTAC | 89910 |
rs78113238 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | UBE3B | GRCh38.p7 | 12:109487634 | CAGGCAGATCCTTGT[G/T]TATCTGCTCTCTATG | 89910 |
rs78160393 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | UBE3B | GRCh38.p7 | 12:109542859 | GCTGCTTAAGTCCCC[A/G]AGTTTATGGTGCTTT | 89910 |
rs78160642 | snp | A/C | 0.0146672 | 0.084371 | intron-variant, upstream-variant-2KB | UBE3B, KCTD10 | GRCh38.p7 | 12:109479140 | TTATAAAGGACTTGA[A/C]ACATAATGGGCACTC | 89910 |
rs78171531 | snp | G/T | 0.0626037 | 0.165477 | intron-variant | UBE3B | GRCh38.p7 | 12:109503666 | ACCTTATCTTTATTG[G/T]CTACATAGTATCTCA | 89910 |
rs78235098 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | UBE3B | GRCh38.p7 | 12:109531370 | ATGGCACACACGCTT[C/T]TCTGTGTATGTGTTA | 89910 |
rs78243182 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109533229 | TCACAAGTGGCCAGT[C/G]GCACCTATTGGGTAT | 89910 |
rs78701986 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | UBE3B | GRCh38.p7 | 12:109530384 | CTTTTAGCTTCCCAG[A/G]GAGATAGAGTTATTG | 89910 |
rs78831476 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | UBE3B | GRCh38.p7 | 12:109500832 | CAGGCAGGCCTGGCC[A/G]TACTCAGGGGTGGCG | 89910 |
rs78922123 | in-del | -/TAAA | | | intron-variant | UBE3B | GRCh38.p7 | 12:109480656 | CCCTGCCTTAAAAAA[-/TAAA]AAAAAAAAGACTTAG | 89910 |
rs78938775 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant, utr-variant-3-prime | UBE3B | GRCh38.p7 | 12:109534294 | TTTTACAGCATTCTA[C/T]TTTTTGTCAATTGGT | 89910 |
rs78953391 | snp | A/G | 0.040671 | 0.13668 | intron-variant | UBE3B | GRCh38.p7 | 12:109508231 | AGACATAATTATTGC[A/G]AAGTGCTTATCACAG | 89910 |
rs79042462 | snp | A/G | 0.0696718 | 0.173152 | intron-variant | UBE3B | GRCh38.p7 | 12:109527854 | GTCAGGCTCAGAGGA[A/G]GGCTTAAATGACAGC | 89910 |
rs79046795 | snp | A/C | 0.000798403 | 0.0199641 | utr-variant-3-prime, intron-variant | UBE3B | GRCh38.p7 | 12:109536233 | GACAGGAATGTATTA[A/C]TATTATTGAAGGTGT | 89910 |
rs79056024 | snp | C/T | 0.0704125 | 0.17392 | intron-variant | UBE3B | GRCh38.p7 | 12:109540368 | GTGCATCACCACAAC[C/T]GGCTAGTTTATTTTG | 89910 |
rs79115204 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109490415 | ATTGTTGAGAAAGCC[C/T]GATTGCTGTTTAAAG | 89910 |
rs79175988 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | UBE3B | GRCh38.p7 | 12:109487679 | CAGATTGCTCTTTGA[A/G]GAGAAGCTCTTCTAT | 89910 |
rs79313296 | snp | A/C/T | 0.00371201 | 0.0429465 | intron-variant, missense, synonymous-codon | UBE3B | GRCh38.p7 | 12:109533956 | CCAGCAGGCTGTGCA[A/C/T]GTCCAGGCTCGCTGC | 89910 |
rs79313644 | snp | A/G | 0.0883596 | 0.190715 | intron-variant | UBE3B | GRCh38.p7 | 12:109515015 | ACCTACCGGGTTCAC[A/G]CCATTCTCCTGCCTC | 89910 |
rs79330589 | snp | C/T | 0.0629771 | 0.165899 | utr-variant-5-prime, intron-variant, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109481675 | GTGAGAAGCTGTTCT[C/T]AGCCACGAGTCCTGT | 89910 |
rs79552766 | snp | G/T | 0.5 | 0 | intron-variant | UBE3B | GRCh38.p7 | 12:109498843 | TGTTTTTTTTTTTTT[G/T]AAGACAGGGTCTCAC | 89910 |
rs79654803 | snp | A/T | 0 | 0 | intron-variant | UBE3B | GRCh38.p7 | 12:109520745 | TTCTGTAGGTTTGAT[A/T]TTTTTTTTTTTTCTT | 89910 |
rs79678874 | snp | C/T | 0.0275645 | 0.114116 | intron-variant | UBE3B | GRCh38.p7 | 12:109509426 | CTCCCTCCCCTTTCC[C/T]CCTACCCCTGATGAT | 89910 |
rs79772173 | snp | A/G | 0.0310518 | 0.120672 | downstream-variant-500B | UBE3B | GRCh38.p7 | 12:109543745 | GGCTGAGGCAGGAGA[A/G]TCACTTGAACCCGGG | 89910 |
rs79933112 | snp | G/T | 0.5 | 0 | intron-variant | UBE3B | GRCh38.p7 | 12:109498841 | TTTGTTTTTTTTTTT[G/T]TGAAGACAGGGTCTC | 89910 |
rs79995789 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109490286 | AAGGAGACCTCAGGG[C/T]TTGTTCCCTCAGATT | 89910 |
rs80069173 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109538449 | CACTTCCTGCCCCAC[A/G]TGGAGGGCAGCCTCC | 89910 |
rs80179710 | snp | A/C | | | intron-variant | UBE3B | GRCh38.p7 | 12:109489043 | TTGCATTATAAACTT[A/C]TTCCTTCCCTGGTAA | 89910 |
rs80188905 | snp | C/T | 0.5 | 0 | intron-variant, utr-variant-5-prime, downstream-variant-500B | UBE3B | GRCh38.p7 | 12:109490979 | CAGTTTACTTTTTTG[C/T]TCTTTTATGTACAAA | 89910 |
rs80317738 | snp | G/T | 0.0607341 | 0.163335 | intron-variant | UBE3B | GRCh38.p7 | 12:109525441 | CAGGGGAAACCTCAG[G/T]CTGGCTGATTCTTAA | 89910 |
rs111256223 | snp | C/T | 0.5 | 0 | intron-variant | UBE3B | GRCh38.p7 | 12:109510237 | ACATATAATTCAGAG[C/T]GAGGGAGATCAAGGA | 89910 |
rs111310114 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109520236 | GGGCCCTGTGCTGTT[C/T]AGCACTGTTTTTATA | 89910 |
rs111446526 | snp | C/T | 0.00586727 | 0.0538443 | intron-variant | UBE3B | GRCh38.p7 | 12:109497947 | GCTCTGTGAGTTCCC[C/T]GTGAAAACCCAATTG | 89910 |
rs111496671 | snp | C/G | 0.5 | 0 | intron-variant | UBE3B | GRCh38.p7 | 12:109539442 | AGAGCAAGAGCCTCA[C/G]AGCATCCTGCCGCTG | 89910 |
rs111499111 | snp | C/T | 0.5 | 0 | utr-variant-3-prime, intron-variant | UBE3B | GRCh38.p7 | 12:109536472 | AAGCACCAATATCAA[C/T]TTCATGTGGATTTTT | 89910 |
rs111500988 | in-del | -/C | 0 | 0 | intron-variant | UBE3B | GRCh38.p7 | 12:109542711 | CAAGGAACGCAGGGA[-/C]TTCCAGCCATCACCC | 89910 |
rs111602438 | snp | A/G | 0 | 0 | utr-variant-3-prime, intron-variant, downstream-variant-500B | UBE3B | GRCh38.p7 | 12:109535105 | TGTCTTTCCTTAGCC[A/G]TCTGAGTGAGCTGTG | 89910 |
rs111609815 | snp | A/G | 0.00896327 | 0.0663422 | intron-variant | UBE3B | GRCh38.p7 | 12:109498219 | CTGATTTAACGGTCT[A/G]CTATTCTTTGCAGCG | 89910 |
rs111624771 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | UBE3B | GRCh38.p7 | 12:109525771 | AATTAGCTCTAATAT[A/G]AGCAAAAGATGAAAA | 89910 |
rs111651117 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | UBE3B | GRCh38.p7 | 12:109489087 | CGTGTGTTTCATATG[A/G]TCATTTCATTCATCT | 89910 |
rs111785749 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | UBE3B | GRCh38.p7 | 12:109530246 | CACTTGTCTGCCTAG[A/C]GATTAAGAAGTGGAA | 89910 |
rs111887173 | snp | A/G | 0.5 | 0 | intron-variant | UBE3B | GRCh38.p7 | 12:109484491 | TCACCTCCCGGGTTC[A/G]AGCAGTTCTCCGGCC | 89910 |
rs112001351 | snp | A/G | 0.00636936 | 0.0560724 | utr-variant-3-prime, intron-variant | UBE3B | GRCh38.p7 | 12:109536082 | GCTGTCACAGTGGCA[A/G]CAAAGCAGGGGCCAC | 89910 |
rs112007581 | snp | A/G | 0.5 | 0 | intron-variant | UBE3B | GRCh38.p7 | 12:109481478 | TTGAAGAGATACAGT[A/G]TAACATTTAGATGAG | 89910 |
rs112020479 | snp | A/T | 0.5 | 0 | intron-variant | UBE3B | GRCh38.p7 | 12:109509452 | ATGATATCATATCAT[A/T]TTATCTGTAGATTTT | 89910 |
rs112037575 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBE3B | GRCh38.p7 | 12:109525247 | CCTGAAAGGCCCCTG[A/G]GCAGGCTGGCACGTG | 89910 |
rs112116453 | snp | C/T | 0.5 | 0 | intron-variant | UBE3B | GRCh38.p7 | 12:109533762 | CACGGACTCAGCCCT[C/T]TCTCGGCAGCCCCTT | 89910 |
rs112193946 | snp | C/T | 0.0414363 | 0.137845 | intron-variant | UBE3B | GRCh38.p7 | 12:109514789 | TGCATGGCCCTGGAA[C/T]CTCTCAGGGCTTTTG | 89910 |
rs112268691 | snp | A/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | UBE3B, KCTD10 | GRCh38.p7 | 12:109478503 | TAGATTATTGAGGCT[A/G]GCCACGGTGGCTCAC | 89910 |
rs112350807 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBE3B | GRCh38.p7 | 12:109480683 | TTAGACATTCTCCCT[A/G]TAGTATGTGGCAGAG | 89910 |
rs112367569 | snp | A/T | 0.0410537 | 0.137264 | intron-variant | UBE3B | GRCh38.p7 | 12:109509460 | ATATCATTTTATCTG[A/T]AGATTTTACAGTAAG | 89910 |
rs112395120 | snp | C/G | 0.0376037 | 0.131863 | intron-variant, upstream-variant-2KB | UBE3B, KCTD10 | GRCh38.p7 | 12:109478896 | GTGGTGGTCATTAAA[C/G]CTGGTGGCCCAGCTT | 89910 |
rs112459254 | snp | A/C | | | intron-variant | UBE3B | GRCh38.p7 | 12:109504739 | ACCATACCTGGGGTA[A/C]CCCAGCGCCTGAGGG | 89910 |
rs112475482 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBE3B | GRCh38.p7 | 12:109498055 | TTGGGACCAGTGGCC[A/G]TGATAGACACATTTG | 89910 |
rs112530776 | snp | C/G | 0.0124951 | 0.0780476 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109490001 | ATTTTATTCTGTGCT[C/G]CAGGTCTGTGACTCC | 89910 |
rs112546474 | snp | C/T | 0 | 0 | intron-variant | UBE3B | GRCh38.p7 | 12:109511836 | TCATCTTGGCTGCAG[C/T]GTGGAGGGCTGGCTA | 89910 |
rs112567398 | snp | C/G | 0.0622301 | 0.165053 | intron-variant | UBE3B | GRCh38.p7 | 12:109516279 | TGGGTTCAAGTGATT[C/G]TCCTGCCTCAACCTC | 89910 |
rs112585284 | snp | C/T | 0.5 | 0 | intron-variant | UBE3B | GRCh38.p7 | 12:109497521 | ACAAACTCCTTCCTC[C/T]TCCATGTATATAGTT | 89910 |
rs112655467 | snp | C/T | 0.5 | 0 | intron-variant | UBE3B | GRCh38.p7 | 12:109513393 | TTCGTGGTTTCAACA[C/T]GAGATTGCACTACAT | 89910 |
rs112689626 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | UBE3B | GRCh38.p7 | 12:109495778 | CAAGTCCTTAAGGCA[C/G/T]AGATTGCTCATGCTA | 89910 |
rs112747408 | snp | A/G | 0.5 | 0 | intron-variant | UBE3B | GRCh38.p7 | 12:109499885 | TTCTTTCTTTCTTCC[A/G]GCTTGTGGTGTTTTG | 89910 |
rs112760787 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109484320 | AGTGGTAAGGACATC[A/G]AAAGGAGTAGCAGGG | 89910 |
rs112836524 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | UBE3B | GRCh38.p7 | 12:109525340 | TACATCCTGGGACAC[A/G]GAACTCTTCTTTGAA | 89910 |
rs112916116 | snp | C/G | 0.0399052 | 0.1355 | intron-variant | UBE3B | GRCh38.p7 | 12:109540849 | GCCAGAACTTGTGCT[C/G]TTGCAAAGAGCAGAA | 89910 |
rs112921563 | snp | A/G | 0.5 | 0 | intron-variant | UBE3B | GRCh38.p7 | 12:109505910 | GTATTGTAAGGGCTC[A/G]TATACAAGGTGACTG | 89910 |
rs113044844 | snp | A/C | | | intron-variant | UBE3B | GRCh38.p7 | 12:109538260 | AGCTGGGTTCTCGCC[A/C]AGCTTGGCGAGTAAA | 89910 |
rs113073132 | snp | C/T | 0.0117469 | 0.075733 | intron-variant | UBE3B | GRCh38.p7 | 12:109501543 | GTGAAGAGTGAGTGA[C/T]GGGAGCAGGCCCAAC | 89910 |
rs113515947 | snp | C/T | | | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109509661 | AAGAGCTGGTCACTA[C/T]CTCCTCTTTCCTGAA | 89910 |
rs113541228 | snp | C/T | 0.5 | 0 | intron-variant, downstream-variant-500B | UBE3B | GRCh38.p7 | 12:109509948 | TTTGCATGTATGTGT[C/T]GAGGATTATTAATGA | 89910 |
rs113700289 | snp | C/G | 0.5 | 0 | intron-variant | UBE3B | GRCh38.p7 | 12:109522186 | TGGTAAGTGAGGAGG[C/G]CCTTCTACGGTGCCC | 89910 |
rs113742687 | snp | A/G | 0.109814 | 0.206997 | intron-variant | UBE3B | GRCh38.p7 | 12:109506611 | CCGCCTCAGCCTCCC[A/G]GAGTGCTGGGATTAC | 89910 |
rs113913176 | snp | A/G | 0.0376037 | 0.131863 | intron-variant, utr-variant-5-prime, downstream-variant-500B | UBE3B | GRCh38.p7 | 12:109490919 | GGACTGTAGGTACAA[A/G]CCACCATGCCTGGCT | 89910 |
rs113970795 | snp | A/G | 0.5 | 0 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109498260 | TTAGAATCCCATGAC[A/G]TGCTTCGTAAATTCA | 89910 |
rs113987841 | snp | A/C | 0.0125728 | 0.0782835 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109483918 | CACTAAAAGAAGTGC[A/C]CTTTGTATTTTCAAG | 89910 |
rs114187931 | snp | C/T | 0.00402863 | 0.0446999 | synonymous-codon, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109507628 | TGAGCTCGGGCCCCA[C/T]GGAGGGTTAAAGCTC | 89910 |
rs114270566 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | UBE3B | GRCh38.p7 | 12:109492185 | CATAGTTTATAAACA[C/T]CTGGTCTAGACTGTG | 89910 |
rs114272666 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | UBE3B | GRCh38.p7 | 12:109498966 | GAGTAGCTGGGACTA[C/T]AAGCGCACACTACCA | 89910 |
rs114293742 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | UBE3B | GRCh38.p7 | 12:109518111 | GAGCATTCTGTTTGC[A/G]TGCTAGACATATAGA | 89910 |
rs114370741 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | UBE3B | GRCh38.p7 | 12:109529730 | GTTCGTGAGTGCTGT[C/T]GTCATTGTCGCCATT | 89910 |
rs114379149 | snp | A/G | 1.64991e-05 | 0.00287215 | intron-variant | UBE3B | GRCh38.p7 | 12:109521341 | TATTTAAGGGGAGCA[A/G]CAGCAGGGCTGACAG | 89910 |
rs114408087 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | UBE3B | GRCh38.p7 | 12:109500856 | GGTGGCGGCTATTAA[C/T]AATATGATGATCAAT | 89910 |
rs114680710 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant, upstream-variant-2KB | UBE3B, KCTD10 | GRCh38.p7 | 12:109478150 | TCAGTTTCCTTCTGT[A/G]TAAATGGAGTAATTA | 89910 |
rs115041378 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | UBE3B | GRCh38.p7 | 12:109492944 | GAATTTGGACCAGCC[G/T]CATTTTTAAGTGCTC | 89910 |
rs115057494 | snp | A/G | 0.00346762 | 0.0414944 | intron-variant | UBE3B | GRCh38.p7 | 12:109511343 | CCGATGTGTCTTTCT[A/G]TTCCCCCACGTGGTT | 89910 |
rs115087613 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | UBE3B | GRCh38.p7 | 12:109494380 | TGTTCCTCACACTGC[C/T]GTGGCATTGATTTTC | 89910 |
rs115205156 | snp | C/T | 0.0244538 | 0.107838 | intron-variant | UBE3B | GRCh38.p7 | 12:109494829 | CTTCCACTGATACGT[C/T]GCTCCCAGTCAGGCA | 89910 |
rs115231746 | snp | C/T | 0.000132448 | 0.00813674 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109507722 | TTCTGTGACTGTTCG[C/T]GGCACCTCATCACGT | 89910 |
rs115234870 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | UBE3B | GRCh38.p7 | 12:109520023 | GGACCAGACGGCAGC[C/T]GAGTGGATGCTGTGG | 89910 |
rs115267443 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBE3B | GRCh38.p7 | 12:109528343 | AGTGGAGCAGTACTC[A/G]TCACCTGCTTCAAAG | 89910 |
rs115360386 | snp | A/T | 0.0138799 | 0.0821421 | intron-variant | UBE3B | GRCh38.p7 | 12:109488455 | AATTAAGACTGACTT[A/T]TAATCCTGACTCAGT | 89910 |
rs115623923 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | UBE3B | GRCh38.p7 | 12:109527151 | CCGTGATGAATTCAA[A/G]TGCCACAGACGGAGG | 89910 |
rs116086983 | snp | A/G | 0.0349115 | 0.127424 | intron-variant | UBE3B | GRCh38.p7 | 12:109492519 | GACTGAGGTGGGCAG[A/G]TCATTTTGAGCTCAG | 89910 |
rs116095906 | snp | A/G | 0.0376037 | 0.131863 | intron-variant | UBE3B | GRCh38.p7 | 12:109514098 | CCTCAGCTCTGCCTG[A/G]CTCACGTGCACAGCA | 89910 |
rs116275699 | snp | A/G | 0.00179678 | 0.0299193 | intron-variant, utr-variant-3-prime | UBE3B | GRCh38.p7 | 12:109534574 | TCCCAATTCAAGGCC[A/G]CGATGTGTGCCTTCA | 89910 |
rs116365526 | snp | A/G | 0.00597247 | 0.0543191 | utr-variant-3-prime, intron-variant | UBE3B | GRCh38.p7 | 12:109536322 | AGATTTCTTCTGAAC[A/G]TGTGTGCGCACGCTG | 89910 |
rs116446457 | snp | C/T | 0.0376037 | 0.131863 | intron-variant | UBE3B | GRCh38.p7 | 12:109481275 | GAGCTGAAATTATGC[C/T]GCTGCACTCCAACCT | 89910 |
rs116449826 | snp | A/C | 0.0134861 | 0.0810011 | intron-variant | UBE3B | GRCh38.p7 | 12:109538919 | CCTACACTGCACATA[A/C]AATCGCTTGGACTGT | 89910 |
rs116502002 | snp | G/T | 0.0130921 | 0.0798413 | intron-variant | UBE3B | GRCh38.p7 | 12:109521389 | TGAAGAGCTGGGCTT[G/T]CTCCTTGCAAGGCAC | 89910 |
rs116505855 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | UBE3B | GRCh38.p7 | 12:109495472 | TCACAGAGTTGTGCA[A/G]CCATCACCTGCTGAG | 89910 |
rs116762332 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | UBE3B | GRCh38.p7 | 12:109523047 | TCTGTGTCCTTTCCC[A/T]CCCTCACCTCTGACA | 89910 |
rs116810347 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | UBE3B | GRCh38.p7 | 12:109484459 | GCAGTGGCGCAGTCT[A/T]GGCTCACTGCCAGTC | 89910 |
rs116884085 | snp | C/T | 0.0517044 | 0.152246 | intron-variant | UBE3B | GRCh38.p7 | 12:109543185 | GGAAATACAGAAGGG[C/T]TGCGTGTGCGTGTGG | 89910 |
rs116889864 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant, utr-variant-3-prime | UBE3B | GRCh38.p7 | 12:109534466 | TGGTGCCAGGGCAGC[A/G]CCCTGCACTCTGCCC | 89910 |
rs116919928 | snp | A/G | 0.00759595 | 0.0611578 | synonymous-codon, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109524473 | TGACCTGGGCCTGAC[A/G]CTGTCTTACGACGAG | 89910 |
rs116921368 | snp | G/T | 0.000784541 | 0.0197903 | intron-variant | UBE3B | GRCh38.p7 | 12:109484004 | GATAATAGCAAACAT[G/T]TATAATACTTCCATA | 89910 |
rs116996075 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UBE3B | GRCh38.p7 | 12:109486239 | GTTTCTTCATGATCC[A/G]GGTAGCTACGTTCTG | 89910 |
rs117009816 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | UBE3B | GRCh38.p7 | 12:109529388 | AAGCATCTGCAGGTC[C/T]GCCTTGCCATAGCAT | 89910 |
rs117189706 | snp | A/G | 0.0517044 | 0.152246 | intron-variant | UBE3B | GRCh38.p7 | 12:109540422 | TGCCATATTGCCCAC[A/G]CTGGTCTTGAACTCC | 89910 |
rs117199998 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | UBE3B | GRCh38.p7 | 12:109493700 | AAAGTCTATAAAATC[A/G]TCAGTGGTGTGCCAA | 89910 |
rs117225198 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109519058 | TATTAAAGTCCTGTA[A/G]GAAGGCTCTTCTTCC | 89910 |
rs117267103 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | UBE3B | GRCh38.p7 | 12:109485119 | CAAATCATACAAAAG[A/G]TGCCAGTTTGCACCT | 89910 |
rs117369894 | snp | C/T | 0.000576383 | 0.0169664 | synonymous-codon, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109521255 | AGGGATTGATCAAGA[C/T]GGTGTTTTTAAGGAG | 89910 |
rs117379832 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109524739 | TGCTTTCTTATATCG[A/C]ATTTTAGGGTAATTC | 89910 |
rs117387539 | snp | C/G | 0.0689305 | 0.172377 | intron-variant | UBE3B | GRCh38.p7 | 12:109506636 | GATTACAGGCGTGAG[C/G]CACAGCACCGGGCTG | 89910 |
rs117685852 | snp | A/T | 0.0376037 | 0.131863 | intron-variant | UBE3B | GRCh38.p7 | 12:109519103 | GGGCTGGAACTCTAG[A/T]ATTCAGAACCGGAAG | 89910 |
rs117721594 | snp | C/G | 0.0685596 | 0.171987 | intron-variant, upstream-variant-2KB | UBE3B, KCTD10 | GRCh38.p7 | 12:109478124 | GGTGAGTTCCCTCAC[C/G]TCTCTGAGCCTCAGT | 89910 |
rs117870959 | snp | C/T | 0.0517044 | 0.152246 | intron-variant | UBE3B | GRCh38.p7 | 12:109528803 | TGCAGTGAGCCGAAT[C/T]GCGCCATTGCACTCC | 89910 |
rs118054605 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UBE3B | GRCh38.p7 | 12:109495703 | AGTATTCCTTATGGG[A/G]AAACAAAGGGATGGG | 89910 |
rs118168308 | snp | C/T | 0.0520825 | 0.152737 | intron-variant | UBE3B | GRCh38.p7 | 12:109518289 | CCTCCCCAGAAGAGG[C/T]CACCGCCACTCAGCT | 89910 |
rs118182918 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | UBE3B | GRCh38.p7 | 12:109523146 | TTTACCCCTTACGGT[C/G]CTCTGACAGGTGTCA | 89910 |
rs137860364 | snp | C/T | 0.000107521 | 0.00733137 | synonymous-codon, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109499655 | CCTACACTTGGGCTC[C/T]CTCAGCCCCAGAGTG | 89910 |
rs137869362 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | UBE3B | GRCh38.p7 | 12:109530167 | AGAGTTGTTTTAGGA[G/T]CCTGTCTCCAGATCT | 89910 |
rs137958276 | snp | C/T | 0.000153988 | 0.00877328 | missense, nc-transcript-variant, downstream-variant-500B | UBE3B | GRCh38.p7 | 12:109509709 | TGATCTGGGATGGAA[C/T]TGTAGGTAAGAGAAA | 89910 |
rs138001412 | snp | A/G/T | 4.94192e-05 | 0.00497067 | missense, utr-variant-5-prime, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109488617 | ACCCTGTACCTCACG[A/G/T]TGCTTGTCACCTTCA | 89910 |
rs138013698 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3B | GRCh38.p7 | 12:109506322 | TAAATTTTTACTAGA[A/G]CAGACCCAAATCTGT | 89910 |
rs138123808 | snp | A/C | 0.0134861 | 0.0810011 | intron-variant | UBE3B | GRCh38.p7 | 12:109540870 | AAGAGCAGAAGCTGG[A/C]AGACCAGCTCAGAGC | 89910 |
rs138205902 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109476623 | CGTGGCGCAGGTATC[C/T]TAACCTCAGGCCCCT | 89910 |
rs138340935 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109528411 | TTTGTATGTATTAAT[A/G]TACAGGTTTGCTGCT | 89910 |
rs138472387 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | UBE3B | GRCh38.p7 | 12:109482611 | GTGTTTTTAACTGGG[A/C]TGATTGTGCATTTTG | 89910 |
rs138490957 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | UBE3B, KCTD10 | GRCh38.p7 | 12:109478551 | TTTGGGAGGCCGAGG[C/T]GGGCGGATCACCTGA | 89910 |
rs138500097 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | UBE3B | GRCh38.p7 | 12:109495518 | GAGACCCTAACCCAG[C/T]GGCACTAGAGGAATT | 89910 |
rs138567017 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBE3B | GRCh38.p7 | 12:109541466 | GCCATGAGGATTAAA[C/T]GAGGTCACATCTGTT | 89910 |
rs138691275 | snp | C/T | 0.00032944 | 0.0128301 | synonymous-codon, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109497830 | TAGCCCTGTGATTGC[C/T]GCACAGTTCTCAGAC | 89910 |
rs138717457 | snp | C/T | 0.000101512 | 0.00712358 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109510424 | GAGCGGGACTGCCGG[C/T]GGCGCTTCACCCCCG | 89910 |
rs138718872 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | UBE3B | GRCh38.p7 | 12:109528941 | AGACGGGCAGATCAC[C/T]CGAGGTCAGGAGTTT | 89910 |
rs138753953 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | UBE3B | GRCh38.p7 | 12:109505734 | ATCACTAAATTGATA[A/C]AATTCTTGGCCTCCT | 89910 |
rs138792545 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109519326 | CACATTCACCTCCCA[A/G]GAGGCATGGATATAA | 89910 |
rs138955857 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109488187 | TCACACAGCTAGTAA[C/G]TGGTGAAGTCAGAAG | 89910 |
rs138996672 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | UBE3B | GRCh38.p7 | 12:109511530 | GTGGCAGCCCAGGTA[C/T]GGAGACCTGACCAGC | 89910 |
rs139010836 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109525075 | GAGAAACCACGCCAT[A/G]AGCTTCTTAATGCAG | 89910 |
rs139031957 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | UBE3B | GRCh38.p7 | 12:109520596 | AGCCCTGTTACTCTT[C/T]GCCTAAAACCTTCTG | 89910 |
rs139093094 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | UBE3B | GRCh38.p7 | 12:109520779 | TCTTTTTTTTACCAT[A/G]AGCTAAAGATACTCT | 89910 |
rs139168400 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBE3B | GRCh38.p7 | 12:109515204 | AGGCGTGAGCCACCG[C/T]GACTGGCCCATCCCC | 89910 |
rs139172208 | snp | A/G | 0.000697199 | 0.0186578 | missense, utr-variant-5-prime, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109483643 | AGAAGGAACGGGAGC[A/G]GGCAGCTGTTGTGAT | 89910 |
rs139202163 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109532575 | TGGCTACTGTTGAGT[C/T]AAAGTGAATGGTTTC | 89910 |
rs139216420 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant, utr-variant-5-prime, downstream-variant-500B | UBE3B | GRCh38.p7 | 12:109490841 | TTTTTTTTTTAAGAG[A/C]CAGGGTTGCCCTGTC | 89910 |
rs139311320 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE3B | GRCh38.p7 | 12:109530803 | CACAGGCAGGCCTCC[C/T]GGTAGGCCAAGCAGT | 89910 |
rs139342666 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | UBE3B | GRCh38.p7 | 12:109507960 | CATCCTTTCAAGGAA[A/G]CTGATCAGTACCACT | 89910 |
rs139428647 | snp | A/G | 3.32508e-05 | 0.00407729 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109511218 | GGGATCTCAAACCTA[A/G]CGTGCTCTTCCAAGA | 89910 |
rs139457994 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBE3B | GRCh38.p7 | 12:109526000 | TTTTAGTAAACGCAC[A/G]TTTTCATCATATTGT | 89910 |
rs139513754 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant, upstream-variant-2KB | UBE3B, KCTD10 | GRCh38.p7 | 12:109479191 | TTGGTTATCACCAAC[C/T]TCTTATTTTCTAATC | 89910 |
rs139534109 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBE3B | GRCh38.p7 | 12:109525843 | GCAAAAGATGAAAAC[A/G]CAAGCTGCCCGTAAT | 89910 |
rs139585965 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | UBE3B | GRCh38.p7 | 12:109484060 | ATTAACTCAGTTCTT[A/T]TAGCAGCTTTATGAG | 89910 |
rs139654189 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | UBE3B | GRCh38.p7 | 12:109530342 | CTCTGCTTGGGAACA[G/T]CAGGGCCAGCTCTCA | 89910 |
rs139676591 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBE3B | GRCh38.p7 | 12:109538533 | TGAGGATTAAATGCA[A/G]TTACATATGACGCAC | 89910 |
rs139807522 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | UBE3B | GRCh38.p7 | 12:109523428 | TGGCCCTGCATCCTC[A/C]TTGGACATAGCTTCC | 89910 |
rs139811986 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBE3B | GRCh38.p7 | 12:109497626 | TTTCATAGCTGCACA[A/G]TATGGCATCAGCAAC | 89910 |
rs139877213 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | UBE3B | GRCh38.p7 | 12:109543195 | AAGGGCTGCGTGTGC[A/G]TGTGGCTTGTCTGAA | 89910 |
rs139898869 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109496289 | CCATTATATGGATAT[A/G]CCACATTTGAGTTGT | 89910 |
rs139919640 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109492418 | TAGAGCAGGTCTGTC[C/G/T]GATGGAAACACAGTT | 89910 |
rs139938449 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109520765 | TTTTTTTTCTTTTTT[C/T]TTTTTTTTACCATGA | 89910 |
rs139973666 | snp | A/T | 0.000153988 | 0.00877328 | missense, utr-variant-3-prime, intron-variant, downstream-variant-500B | UBE3B | GRCh38.p7 | 12:109534753 | CTGCGCTACGCCATC[A/T]GCATGAACACGGGCT | 89910 |
rs140000478 | snp | A/G | 0.000153988 | 0.00877328 | synonymous-codon, utr-variant-3-prime, intron-variant, downstream-variant-500B | UBE3B | GRCh38.p7 | 12:109534665 | GCCAGGCGGCCGCCT[A/G]CCCACCTCCTCCACC | 89910 |
rs140008717 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBE3B | GRCh38.p7 | 12:109506718 | TAGCACTGAGTAGTT[G/T]TAACAGTGTTAGACT | 89910 |
rs140073922 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109540718 | AGCTATTGTGAAGTC[A/C]TTCTGGCCCTTCCAG | 89910 |
rs140112589 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | UBE3B | GRCh38.p7 | 12:109516457 | GCTGGGATTACAGGC[A/G]TGAGCCCCCACGCCC | 89910 |
rs140114450 | snp | C/T | 0.000307953 | 0.0124049 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109521188 | TCTCCCAGCACGCCA[C/T]GAAGGGGGTCATCCG | 89910 |
rs140239049 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | UBE3B | GRCh38.p7 | 12:109499577 | GCAGGGAGCAGGGCC[A/G]GGAGGCACCAAAATG | 89910 |
rs140240416 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109510265 | GGACTTGATGACAAC[G/T]GCGGAAGACAAGAGC | 89910 |
rs140255043 | snp | A/T | 2.23391e-05 | 0.00334202 | intron-variant | UBE3B | GRCh38.p7 | 12:109490086 | ATTTGCATTCAGCAT[A/T]CCTGGTGTCCTCCTC | 89910 |
rs140303194 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBE3B | GRCh38.p7 | 12:109481846 | GTGCAAAAGTAATTA[C/T]GACTTAGTGTTTTTT | 89910 |
rs140482099 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | UBE3B | GRCh38.p7 | 12:109482148 | TTAATACCTCTAGGA[A/G]ATAATACTATTAAGT | 89910 |
rs140484084 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | UBE3B | GRCh38.p7 | 12:109531451 | TTCCTACTTGACAGA[A/G]TATCAATGAACATTT | 89910 |
rs140524384 | snp | A/T | 0.0103295 | 0.0711199 | intron-variant | UBE3B | GRCh38.p7 | 12:109527982 | AGTAGGTAGTCACTC[A/T]CTCTCCCCACATAGG | 89910 |
rs140603482 | snp | G/T | 0.00133851 | 0.0258353 | missense, utr-variant-5-prime, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109486017 | CTCTTTGCAGAGATT[G/T]GAGAAGTTGTGTCGC | 89910 |
rs140630274 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UBE3B | GRCh38.p7 | 12:109486724 | AGAGGAATTTTGATT[C/G]TGTTATCAATATGAG | 89910 |
rs140643064 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBE3B | GRCh38.p7 | 12:109494254 | CCAGAACTCATACTC[C/T]TTCTTCTTATTCTTT | 89910 |
rs140644072 | snp | A/G | 0.0520825 | 0.152737 | intron-variant | UBE3B | GRCh38.p7 | 12:109481062 | GTGAGCCAATATCGC[A/G]CCACTGCACTCCAGC | 89910 |
rs140714011 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3B | GRCh38.p7 | 12:109517640 | TGCTCATCCTGCCAG[C/T]GATAGAATTGGTGAC | 89910 |
rs140774225 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3B | GRCh38.p7 | 12:109505705 | GAAAATGTGAGGTCT[A/G]AGCTCTAGGCATAAT | 89910 |
rs140802141 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | UBE3B | GRCh38.p7 | 12:109536297 | TTCTCCAAACGCTCG[A/G]TTCCTTTGAAGATTT | 89910 |
rs140834231 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | UBE3B | GRCh38.p7 | 12:109524172 | TGAACTCACAGCTTG[C/T]GAAGTCCCAGAAGGA | 89910 |
rs140945794 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, downstream-variant-500B | UBE3B | GRCh38.p7 | 12:109509812 | GCTTTATTGTCTCTC[C/T]AAGTTAATAGAAGGT | 89910 |
rs141020440 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109507135 | CTAAAAATATTTACT[A/C]TTTGGCTGTTTCCTG | 89910 |
rs141058225 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | UBE3B | GRCh38.p7 | 12:109503450 | CTTTTAAAAAGTTTC[C/T]GTTTTCTGAGTAAAG | 89910 |
rs141063517 | snp | A/G | 0.000115637 | 0.00760295 | missense, utr-variant-5-prime, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109486547 | AGAACATTTTGTGGT[A/G]CTGCTGTGATTTTCT | 89910 |
rs141086391 | snp | A/C/G/T | 0.00047768 | 0.015448 | synonymous-codon, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109507634 | CGGGCCCCACGGAGG[A/C/G/T]TTAAAGCTCTTCTTG | 89910 |
rs141122285 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | UBE3B | GRCh38.p7 | 12:109532296 | GAATGCTCGTCACAG[C/T]GTGGAAACACAAAAA | 89910 |
rs141158851 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBE3B | GRCh38.p7 | 12:109490285 | GAAGGAGACCTCAGG[A/G]CTTGTTCCCTCAGAT | 89910 |
rs141197336 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | UBE3B | GRCh38.p7 | 12:109525015 | TGTGTCCTGGTGGAG[A/G/T]TCCCTGCATGAGGCT | 89910 |
rs141298922 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, missense | UBE3B | GRCh38.p7 | 12:109534045 | GTCTCAAGCCTGGCC[C/T]ACTGTGGGTGCTCAA | 89910 |
rs141309827 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | UBE3B | GRCh38.p7 | 12:109518947 | TTGGACACAAGGGGG[C/T]GTCAGTAAGCTGATC | 89910 |
rs141319164 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | UBE3B | GRCh38.p7 | 12:109526925 | CATTTATTTTTTGCA[A/G]TAGCACTTCTAAGGT | 89910 |
rs141528351 | snp | C/T | 0.000220091 | 0.0104879 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109483590 | GAGAGCATGGTTCAT[C/T]GATAGAGCCCGTCAG | 89910 |
rs141709807 | snp | G/T | 0.000131802 | 0.00811688 | missense, intron-variant | UBE3B | GRCh38.p7 | 12:109530047 | ATCTCTGGCGACAAT[G/T]CTGAGATTGATCTGG | 89910 |
rs141723992 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | UBE3B | GRCh38.p7 | 12:109510665 | ACCAAATATGATTAG[A/C]GTTAATTAATGGCAA | 89910 |
rs141727825 | snp | C/G | 0.00358779 | 0.0422022 | utr-variant-3-prime, intron-variant | UBE3B | GRCh38.p7 | 12:109535960 | CCCACCCTCTCCCAC[C/G]TCATGCTCCTGCACC | 89910 |
rs141728926 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109501061 | CCAGCTATGAGGAGG[A/G]AGGCAGTGCAGTGGG | 89910 |
rs141766317 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | UBE3B | GRCh38.p7 | 12:109533047 | ACCAGCCTCCGCCTC[A/G]CCCTCACCGTCTCCC | 89910 |
rs141787174 | in-del | -/C | 0.0577344 | 0.159793 | intron-variant | UBE3B | GRCh38.p7 | 12:109515869 | TCTTAAGAATAAGGA[-/C]GAGAGGGTTCCTTTC | 89910 |
rs141825379 | snp | A/G | 2.04882e-05 | 0.00320058 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109510428 | GGGACTGCCGGCGGC[A/G]CTTCACCCCCGAGGA | 89910 |
rs141847608 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109520111 | AGAAATGTGGCATGG[C/T]CTTCATAGGACAGCA | 89910 |
rs141849006 | snp | A/G | 0.000131841 | 0.00811808 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109503035 | CAGGTCTCCTAAAGC[A/G]TGCTTTTCAAAAGTC | 89910 |
rs141861530 | snp | A/G | 0.000197873 | 0.00994471 | intron-variant, missense, downstream-variant-500B, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109491058 | AGATATTGTTAACCC[A/G]TGGCCTGGCAAGACC | 89910 |
rs141870078 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109538406 | GGGCTCTGGAATCGC[A/G]GAGATGTGTGAGCAA | 89910 |
rs141901011 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | UBE3B | GRCh38.p7 | 12:109505833 | TGCTGGCTAATATAC[C/T]TTCCCCAAACAGTTC | 89910 |
rs141966647 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | UBE3B, KCTD10 | GRCh38.p7 | 12:109478374 | ACTGTTTTGGATATA[C/T]ATGGATTCAGATTCA | 89910 |
rs142128091 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109520614 | CTAAAACCTTCTGCA[A/G]CTCCCATTACCTTCA | 89910 |
rs142137568 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109476139 | CTCCACCCCAAGAAT[A/G]TCTGATTCAGTAGTC | 89910 |
rs142297728 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | UBE3B | GRCh38.p7 | 12:109525328 | CTCAAGCTTCCCTAC[A/C]TCCTGGGACACAGAA | 89910 |
rs142331810 | in-del | -/A | 0.0667028 | 0.170006 | intron-variant | UBE3B | GRCh38.p7 | 12:109494782 | AGATCACACCCCTCC[-/A]AACATTGAGGCAGCC | 89910 |
rs142366180 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBE3B | GRCh38.p7 | 12:109499907 | GGTGTTTTGTTTCTT[A/G]TTATAAAAATAATAT | 89910 |
rs142435033 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | UBE3B | GRCh38.p7 | 12:109507458 | TTTCACGCACATTAA[A/G]TGTTCATGGATAGGT | 89910 |
rs142438371 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | UBE3B | GRCh38.p7 | 12:109535820 | GGTTTTTTGTTTTTT[C/T]TTTAAACTTCATTTC | 89910 |
rs142507321 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBE3B | GRCh38.p7 | 12:109517098 | GAGACCCAGCAGTGT[C/T]TTCCTTTACCCCATG | 89910 |
rs142508848 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109499156 | TGCGAATGTTCACAC[A/G]AGTGACGTTGACTAA | 89910 |
rs142513921 | in-del | -/AAAG | 0.269538 | 0.249235 | intron-variant | UBE3B | GRCh38.p7 | 12:109528858 | CCATCTCAAAAAAAA[-/AAAG]AAAAGAAAAAGAAAA | 89910 |
rs142548129 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109537249 | GTGCCAGGCGTTGTT[C/T]CCTTAGTGAGGATTG | 89910 |
rs142548986 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | UBE3B | GRCh38.p7 | 12:109495290 | CTCATTGCTATTGGA[A/G]CACATTAGCTAGAAG | 89910 |
rs142614983 | snp | A/T | 0.00755907 | 0.0610114 | intron-variant | UBE3B | GRCh38.p7 | 12:109541359 | AGCTCGGATCACCAC[A/T]CCCACCCTCAGTGAC | 89910 |
rs142615255 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | UBE3B | GRCh38.p7 | 12:109495837 | CAGTTTTCCACCCTG[A/G]GTGGGCCAGGTGTTC | 89910 |
rs142628764 | snp | C/T | 0.000299915 | 0.012242 | intron-variant | UBE3B | GRCh38.p7 | 12:109486444 | CTCTATAACAGCCCA[C/T]GACATTCCTCTTTTT | 89910 |
rs142640939 | snp | G/T | 1.71687e-05 | 0.00292986 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109521515 | CCTGCAGCTCTTCGA[G/T]TTTGTGGGGAAGATG | 89910 |
rs142691244 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109525850 | ATGAAAACGCAAGCT[A/G]CCCGTAATGCCAGTG | 89910 |
rs142750926 | snp | A/G | 4.94189e-05 | 0.00497062 | synonymous-codon, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109497860 | CAATCTGATTCGGCC[A/G]TTCCTCATCCACATC | 89910 |
rs142757108 | snp | C/T | 3.53738e-05 | 0.00420543 | missense, utr-variant-5-prime, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109483559 | TTGCAAACATGTTCA[C/T]CCTGTCTCAGACCTC | 89910 |
rs142826229 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | UBE3B | GRCh38.p7 | 12:109531779 | AGTTTTCCCAGAAGT[G/T]CCTCATGGGCAAAGC | 89910 |
rs142891559 | snp | G/T | 0.0252325 | 0.109451 | intron-variant | UBE3B | GRCh38.p7 | 12:109480406 | TAATCCTAACATTTT[G/T]GGAGGCCAAGGCAGG | 89910 |
rs142917892 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3B | GRCh38.p7 | 12:109512265 | ACCTGGGCGAGGTGG[C/T]TGGGGAGTCAGACGG | 89910 |
rs142936386 | snp | A/T | 0.0554779 | 0.157039 | intron-variant, upstream-variant-2KB | UBE3B, KCTD10 | GRCh38.p7 | 12:109478657 | GTGGTGGCGGGCGCC[A/T]TTAATCCCAGCGACT | 89910 |
rs142985308 | in-del | -/TAGGGTTT | 0.0119091 | 0.0762411 | intron-variant | UBE3B | GRCh38.p7 | 12:109484945 | TATTTTTTGTAGAGA[-/TAGGGTTT]TACCTTATTGCCCAG | 89910 |
rs142990151 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBE3B | GRCh38.p7 | 12:109542845 | GAGGATGAATGTCTG[C/T]TGCTTAAGTCCCCGA | 89910 |
rs143061964 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109539868 | GCAGCAGCTCCTCCA[C/G]CCGGGGACCAGCAGT | 89910 |
rs143131356 | snp | C/T | 0.0267878 | 0.112589 | intron-variant | UBE3B | GRCh38.p7 | 12:109514974 | GCTGGAGTGCAGTGG[C/T]GCGATCTCAGCTCAC | 89910 |
rs143164188 | in-del | -/G | 0.200801 | 0.245111 | intron-variant, upstream-variant-2KB | KCTD10, UBE3B | GRCh38.p7 | 12:109475518 | ACCTGTGCTTGCCTG[-/G]GGCTACACCCCAGAT | 89910 |
rs143225792 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109513055 | TCTGTTGGCAGCTCC[C/T]GTTTGCATGTGGGGC | 89910 |
rs143237475 | snp | A/G | | | utr-variant-5-prime, intron-variant, upstream-variant-2KB, nc-transcript-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109478051 | CGAGGAAAGACTCTG[A/G]GCCCCAGGACTCACC | 89910 |
rs143362590 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | UBE3B | GRCh38.p7 | 12:109528704 | ACTAAAAATACAAAA[A/C]TTAGCTGGACATGGT | 89910 |
rs143394928 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | UBE3B | GRCh38.p7 | 12:109483278 | ATCCTATGCCAGGTG[C/G]TGTGCTCTTTCCCTT | 89910 |
rs143397408 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | UBE3B | GRCh38.p7 | 12:109497571 | AAAGTTCATTGTAGC[A/C]TGAGCATTCTCTCAT | 89910 |
rs143400724 | snp | C/T | 0.0517044 | 0.152246 | intron-variant | UBE3B | GRCh38.p7 | 12:109484538 | CTGGAACTATAGGCT[C/T]GTGCCACCACGCCCA | 89910 |
rs143424446 | snp | C/T | 0.000115366 | 0.00759405 | synonymous-codon, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109523992 | GGGAATTGTGGTGGA[C/T]GTGCCATTTGCATCC | 89910 |
rs143479081 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3B | GRCh38.p7 | 12:109505213 | GATTATAGAAAATAA[C/T]GCTTGTTTTTAAAAT | 89910 |
rs143522651 | snp | A/G | 3.34141e-05 | 0.00408729 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109499695 | GAGACAGATGGGTTC[A/G]TGAGTTTGCTCACCC | 89910 |
rs143536763 | snp | A/T | 1.64871e-05 | 0.00287111 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109483888 | TGACTTTTTTAAAGC[A/T]GATGACCCTGAGTCC | 89910 |
rs143576048 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | UBE3B | GRCh38.p7 | 12:109489218 | TTCCTCACAGAACTT[A/T]AAGTCCGATGAGGAA | 89910 |
rs143650256 | in-del | -/TT | | | intron-variant | UBE3B | GRCh38.p7 | 12:109516188 | TTTTTTTTTTTTTTT[-/TT]GAGACAGAGTCTCAC | 89910 |
rs143711320 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109519614 | ACTCCTGCAGGCAGA[C/T]AGGAACTTGATGGAA | 89910 |
rs143822238 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | UBE3B | GRCh38.p7 | 12:109507034 | GAACCTCGTCTGGTT[C/G]TGAGGGCTGCCTGAT | 89910 |
rs143901217 | snp | C/T | 0.000593237 | 0.0172124 | intron-variant | UBE3B | GRCh38.p7 | 12:109533453 | TCCCCACTGACCCTG[C/T]TTTGTGTTGCAGTTC | 89910 |
rs143939312 | snp | A/G | 0.0121634 | 0.0770307 | intron-variant | UBE3B | GRCh38.p7 | 12:109511353 | TTTCTATTCCCCCAC[A/G]TGGTTCCTGCCTTTC | 89910 |
rs143958086 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBE3B | GRCh38.p7 | 12:109521628 | CACATACACATATGT[G/T]ATCAGGCTTGGCCAT | 89910 |
rs144106525 | snp | A/G | 3.39801e-05 | 0.00412176 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109483701 | TCGGAGTCGACTGCA[A/G]AGAGATATCAGGTAA | 89910 |
rs144110274 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | UBE3B | GRCh38.p7 | 12:109534333 | AATTCGCTGTGAACC[A/G]GAAGGCCCCATTTCC | 89910 |
rs144122078 | in-del | -/GCT | 0.0644693 | 0.167566 | intron-variant | UBE3B | GRCh38.p7 | 12:109543006 | TCACAGGAACCGGCA[-/GCT]GCTGCTCAGCCCCAG | 89910 |
rs144247710 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | UBE3B | GRCh38.p7 | 12:109492770 | TCAAAATAAAAGGGA[A/C]ATTTAGTATAATGAT | 89910 |
rs144274799 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBE3B | GRCh38.p7 | 12:109542206 | TGGCGCCTGTGTCAT[C/T]ACTGCCTCCTCCTCA | 89910 |
rs144278603 | snp | A/G | 4.94727e-05 | 0.00497332 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109501378 | TCTCCTAGCCTTAAC[A/G]AGTCAATGCACTTGA | 89910 |
rs144343146 | snp | A/C | 0.000153988 | 0.00877327 | missense, utr-variant-5-prime, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109486033 | GAGAAGTTGTGTCGC[A/C]GCATCCTGAGCAGCA | 89910 |
rs144475884 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | UBE3B | GRCh38.p7 | 12:109517751 | CCAGCTGCAGTTCCC[C/T]ATGAGCCTGTCCTGT | 89910 |
rs144512513 | snp | C/G/T | 4.94192e-05 | 0.00497067 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109497882 | ATCCACATCATGTCT[C/G/T]TGCCTGCTCTGGTGA | 89910 |
rs144569255 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBE3B | GRCh38.p7 | 12:109501291 | AGCTCCGAGTGGAAG[A/G]CCATTAGGAACTGTG | 89910 |
rs144573357 | snp | A/C/T | 6.59156e-05 | 0.00574056 | missense, intron-variant | UBE3B | GRCh38.p7 | 12:109530633 | CCTCCGACTTCACAC[A/C/T]GGATGAGAGAGCTAT | 89910 |
rs144602717 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant, downstream-variant-500B | UBE3B | GRCh38.p7 | 12:109510066 | AGTCCACCTCCCGAA[G/T]TGTCTCCAATTGCTC | 89910 |
rs144623099 | snp | C/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109505708 | AATGTGAGGTCTAAG[C/G]TCTAGGCATAATCAC | 89910 |
rs144651250 | in-del | -/T | 0.08872 | 0.19102 | intron-variant | UBE3B | GRCh38.p7 | 12:109509552 | TTTTTTCTCTTCGCC[-/T]TTTTTTCAGTGTGGA | 89910 |
rs144815408 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | UBE3B | GRCh38.p7 | 12:109504009 | GAGAGCCAAGTTCTT[C/T]GTTCTCAAGGGGATT | 89910 |
rs144938974 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109509289 | CTTTAAGTTCTAGGA[C/T]ACATGTGCTGAAAGT | 89910 |
rs144981958 | in-del | -/GC | | | intron-variant | UBE3B | GRCh38.p7 | 12:109486604 | AAAAAAAAAAAAAAA[-/GC]AAAACCAGAAACAGT | 89910 |
rs144985467 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBE3B | GRCh38.p7 | 12:109526981 | TTAGGAGTTTAATAA[C/T]GGCCCTAGATGCTGA | 89910 |
rs145019742 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109525070 | CTCAGGAGAAACCAC[A/G]CCATGAGCTTCTTAA | 89910 |
rs145048182 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | UBE3B | GRCh38.p7 | 12:109480471 | ACCTGGGCAATATAG[C/T]GAGACCCCACCTCTA | 89910 |
rs145106370 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | UBE3B | GRCh38.p7 | 12:109526660 | GGCGGATCACGAGGT[C/T]AGGAGTTCGAGACCA | 89910 |
rs145145268 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | UBE3B | GRCh38.p7 | 12:109535375 | CGCTATGGACACCGT[C/G]AGTCCAAGGCGCTGC | 89910 |
rs145147821 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109520410 | GGTTCTGGGGCTGTG[C/T]ATGTTGAGGTCTGGA | 89910 |
rs145230392 | snp | C/T | 3.29533e-05 | 0.00405901 | synonymous-codon, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109501414 | AAACAGCTGCAGTTC[C/T]TGTGGGGGGTGCCTC | 89910 |
rs145232742 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | UBE3B | GRCh38.p7 | 12:109523540 | CTGGCTTTTCCTCCC[A/G]GAAGCTCCCCAACTC | 89910 |
rs145263653 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBE3B | GRCh38.p7 | 12:109524902 | TCTCAGCATACAGAG[C/T]AGAGCAGGGAGCAGA | 89910 |
rs145273683 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant, upstream-variant-2KB | KCTD10, UBE3B | GRCh38.p7 | 12:109475559 | AGTATCTCAGAGATG[C/T]GGAGGGGTGGCTGAT | 89910 |
rs145274967 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | UBE3B | GRCh38.p7 | 12:109526303 | TCTCATCTCCGGGAA[A/G]CTTTATTTCCCCATT | 89910 |
rs145368333 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | UBE3B | GRCh38.p7 | 12:109502595 | CAAAGGTAGAATATC[A/G]TTCAAAACCAGGTGT | 89910 |
rs145480324 | snp | C/T | 8.23757e-05 | 0.00641725 | synonymous-codon, intron-variant | UBE3B | GRCh38.p7 | 12:109530565 | GCACACAGTCTACTA[C/T]GGTGGTTTCCATGGA | 89910 |
rs145503739 | snp | C/T | 1.73249e-05 | 0.00294315 | missense, utr-variant-3-prime, intron-variant, downstream-variant-500B | UBE3B | GRCh38.p7 | 12:109534729 | AAGAAGAGCGTCCTC[C/T]GCGAGAAGCTGCGCT | 89910 |
rs145533524 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | UBE3B | GRCh38.p7 | 12:109536760 | CGTTCACACTTGGGT[A/G]TCTGGGCTTAGGGAG | 89910 |
rs145550994 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109539313 | CACCACCCTCTGGAG[C/T]GTGGGGTCAGAATGG | 89910 |
rs145569956 | snp | A/G | 3.29451e-05 | 0.00405851 | synonymous-codon, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109521210 | GGTCATCCGTGTGAA[A/G]TTTGTCAATGACCTC | 89910 |
rs145582760 | in-del | -/C | | | intron-variant | UBE3B | GRCh38.p7 | 12:109533315 | GTGCCAGTTTTGGGG[-/C]CCAGATCCACCCCGC | 89910 |
rs145618947 | snp | C/T | 1.64773e-05 | 0.00287026 | synonymous-codon, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109498256 | TGTTTTAGAATCCCA[C/T]GACATGCTTCGTAAA | 89910 |
rs145635869 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | UBE3B | GRCh38.p7 | 12:109486780 | TTAAACTGCTTGCCA[C/T]GCCACAGCCTCCATG | 89910 |
rs145638057 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109485831 | GGCCACCAGTTGGAG[A/T]ACCCTTTAGTCTTTA | 89910 |
rs145654458 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3B | GRCh38.p7 | 12:109482579 | TGGAAGTCTGGATTT[C/T]TGAATAATTCATTTC | 89910 |
rs145724590 | snp | A/G | 1.64757e-05 | 0.00287012 | synonymous-codon, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109497824 | TGTGTCTAGCCCTGT[A/G]ATTGCTGCACAGTTC | 89910 |
rs145733072 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109498151 | CTCCATAACCACGGG[C/T]GATCTGCAAGTGATC | 89910 |
rs145812083 | snp | A/G | 9.88826e-05 | 0.00703076 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109521157 | TGGCAGGACGGCTAC[A/G]AGCAGCTTAGGCAGC | 89910 |
rs145835615 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | UBE3B | GRCh38.p7 | 12:109495444 | GCATACCATTCCCTG[A/G]CATTTAGTATGTTCA | 89910 |
rs145839172 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBE3B | GRCh38.p7 | 12:109504496 | CAGGTTGTTGGCCCA[A/G]CCACCTGTGTGGATG | 89910 |
rs146013622 | snp | C/G/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109492356 | GGGACAGCACAGATA[C/G/T]AGAAAACTTCCAGCA | 89910 |
rs146020872 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109500185 | TGCTAAAACAAGACA[A/G]ATGATTCAAAGGGAA | 89910 |
rs146032375 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | UBE3B | GRCh38.p7 | 12:109496225 | ATCAGAGTTCATCCA[C/T]GTTGTAGCATGGATC | 89910 |
rs146084947 | snp | C/G | 0.0182019 | 0.0936463 | intron-variant | UBE3B | GRCh38.p7 | 12:109497600 | ATGTCAGTAAAATTT[C/G]AAAACTGGTTTTTCA | 89910 |
rs146206475 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109516648 | GTAGCACATGTTAAG[C/G]CATCCCATTCTGCTT | 89910 |
rs146283937 | snp | A/C/T | 4.23238e-05 | 0.00460005 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109510434 | GCCGGCGGCGCTTCA[A/C/T]CCCCGAGGACCACTG | 89910 |
rs146300392 | snp | C/G | 0.000397595 | 0.0140939 | synonymous-codon, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109499709 | CGTGAGTTTGCTCAC[C/G]CAGACGCTGTGCTAC | 89910 |
rs146327094 | snp | A/G | 0.0084891 | 0.0645948 | intron-variant, utr-variant-3-prime | UBE3B | GRCh38.p7 | 12:109534564 | ACTAGGCCCTTCCCA[A/G]TTCAAGGCCACGATG | 89910 |
rs146377005 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | UBE3B | GRCh38.p7 | 12:109520778 | TTCTTTTTTTTACCA[C/T]GAGCTAAAGATACTC | 89910 |
rs146384073 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | UBE3B, KCTD10 | GRCh38.p7 | 12:109478453 | TAATATGAATAGTCT[C/T]TTTAAGTCGTGTTTC | 89910 |
rs146533231 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | UBE3B | GRCh38.p7 | 12:109486902 | GTACAGAAGCCGAAC[A/G]TGAGCACAGCTAGTA | 89910 |
rs146581108 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | UBE3B | GRCh38.p7 | 12:109493324 | TCAAGCTCAGGAGCA[G/T]CTCTGCCTCCCCCTC | 89910 |
rs146650861 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | UBE3B | GRCh38.p7 | 12:109510075 | CCCGAAGTGTCTCCA[A/G]TTGCTCAGGACAAAG | 89910 |
rs146700174 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | UBE3B | GRCh38.p7 | 12:109513875 | ATGGGCTGTCTTGTT[A/G]CCCCTCCGCCCATCT | 89910 |
rs146773551 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | UBE3B | GRCh38.p7 | 12:109527604 | TCAGGAGAACAGACC[C/G]TGTTTTCATAATGAT | 89910 |
rs146793757 | in-del | -/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109512930 | GTTCTGTGGCTTTAC[-/T]TTTTCCAAAAGATAG | 89910 |
rs146809895 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109486643 | TCATTTTCACCTGTA[A/G]ACTTTAGTCTGTATT | 89910 |
rs146821281 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109482127 | TTTCAATAACACGTA[A/G]TTAATTTAATACCTC | 89910 |
rs146821585 | snp | C/T | 0.0399052 | 0.1355 | intron-variant | UBE3B | GRCh38.p7 | 12:109531041 | TACAGATAAGCAAAA[C/T]ATTAAACAATTGCTG | 89910 |
rs146831943 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109499462 | AAGTCAGCTTGGCCC[A/G]TTTCTTACCTTTGCA | 89910 |
rs146949851 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | UBE3B | GRCh38.p7 | 12:109533081 | TTCTCCTCACATGGT[A/C]TCTCTGTGGGAGGGT | 89910 |
rs146992000 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBE3B | GRCh38.p7 | 12:109519241 | GGCCTGGAAGCCAGG[C/T]ATCCCTTTTCTAGCT | 89910 |
rs147087801 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109494558 | TTCTCCTCAACCCCC[A/C]ACCATGTCTGGCCCT | 89910 |
rs147096850 | snp | A/G | 0.00827029 | 0.063771 | intron-variant | UBE3B | GRCh38.p7 | 12:109488557 | TCTTAATCTTGCTGT[A/G]TTTATTGTTTCCAGC | 89910 |
rs147097299 | snp | C/T | 0.0130921 | 0.0798413 | utr-variant-3-prime, intron-variant | UBE3B | GRCh38.p7 | 12:109536024 | AGGAAGGCCCAGTCC[C/T]TCCTCTGCTCTCCTC | 89910 |
rs147126682 | snp | A/G | 0.000197687 | 0.00994004 | synonymous-codon, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109503054 | TTTTCAAAAGTCGGC[A/G]TCAGTCCGGAATATT | 89910 |
rs147151278 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109485046 | ACAGGCGTGAGCTAC[A/C/T]ATCAATGTTCTAATT | 89910 |
rs147167534 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBE3B | GRCh38.p7 | 12:109489237 | TCCGATGAGGAAAAC[A/G]GGCATTAAATAGATG | 89910 |
rs147257008 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109507041 | GTCTGGTTCTGAGGG[C/T]TGCCTGATGGATGAA | 89910 |
rs147273882 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | UBE3B | GRCh38.p7 | 12:109511470 | TACACCCAGTGCTGG[G/T]GTACAGAGCTGGAGA | 89910 |
rs147362068 | in-del | -/A | | | intron-variant | UBE3B | GRCh38.p7 | 12:109480669 | AAAAAAAAAAGACTT[-/A]AGACATTCTCCCTAT | 89910 |
rs147363978 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109525895 | GTGATAGTGTGTTAC[C/T]TGCGTCCCTTGAGAC | 89910 |
rs147402736 | snp | A/G | 6.66123e-05 | 0.00577076 | missense, utr-variant-5-prime, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109483610 | GAGCCCGTCAGGCAC[A/G]AGAAGAAAGGCTTGT | 89910 |
rs147469544 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE3B | GRCh38.p7 | 12:109543194 | GAAGGGCTGCGTGTG[C/T]GTGTGGCTTGTCTGA | 89910 |
rs147492786 | snp | A/G/T | 5.06131e-05 | 0.00503035 | synonymous-codon, missense, utr-variant-3-prime, intron-variant, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109534650 | CATCCGCAAGCGGGA[A/G/T]CCAGGCGGCCGCCTG | 89910 |
rs147644768 | snp | G/T | 0.00636936 | 0.0560724 | upstream-variant-2KB, intron-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109476096 | TTAGTCTAATCCCTT[G/T]CAGGGCTTGTTAAAA | 89910 |
rs147740393 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109502828 | TATTCTGAAGAGATC[C/T]TTGGGTTGTACCTAA | 89910 |
rs147749542 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109498588 | ACATTAGATGTCAGC[C/G]TTTAGCTTCCTGGCA | 89910 |
rs147845375 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBE3B | GRCh38.p7 | 12:109522082 | TCAGCCGTGTGACCA[C/T]GTGCCTTCAAGTTTC | 89910 |
rs147855527 | snp | A/C | | | intron-variant | UBE3B | GRCh38.p7 | 12:109518379 | GGCCAAAATTCAGAT[A/C]TTCCATGTTGTGAAC | 89910 |
rs147952492 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | UBE3B | GRCh38.p7 | 12:109538964 | TGCATGGCCAGGCTC[G/T]GTAGCTCATGCCTGT | 89910 |
rs148011437 | snp | A/C/G | 0.000559979 | 0.0167237 | synonymous-codon, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109497911 | GACTCATCTCAGCAC[A/C/G]GTGACCCCTGAGGTA | 89910 |
rs148058352 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | UBE3B | GRCh38.p7 | 12:109495721 | ACAAAGGGATGGGCC[A/G]AAATAAAGGGATGGG | 89910 |
rs148075761 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109520059 | GCCTGTCTAACCTGC[A/G]AAGCATGTGACAGTG | 89910 |
rs148129849 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109525648 | TGAAGTTGAAAGAAG[C/T]AGTTGATTTTACAGA | 89910 |
rs148216756 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | UBE3B | GRCh38.p7 | 12:109499489 | TGCACCACACAGCAG[C/T]CTCCGGCATTGACAG | 89910 |
rs148272503 | snp | C/T | 0.000370989 | 0.0136146 | intron-variant, missense | UBE3B | GRCh38.p7 | 12:109534005 | AAAGGAGAAGGAAAG[C/T]CTTCAGGGTTACGGA | 89910 |
rs148287557 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBE3B, KCTD10 | GRCh38.p7 | 12:109478338 | GCCCTGGATCTTGTT[G/T]GTTTTACTTAGTGAT | 89910 |
rs148340310 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109483433 | TCCTGAGTATCTCTG[C/G]TGCCCAGGTCCCTGC | 89910 |
rs148438432 | snp | A/G | 0.00580271 | 0.0535507 | intron-variant | UBE3B | GRCh38.p7 | 12:109516718 | TGTTTTTATGGAATC[A/G]TCAGTTTGCTGACCC | 89910 |
rs148446468 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | UBE3B | GRCh38.p7 | 12:109486219 | AAAGTACAAATGATT[C/G]CTTAGTTTCTTCATG | 89910 |
rs148546824 | in-del | -/A | 0.0681886 | 0.171594 | intron-variant | UBE3B | GRCh38.p7 | 12:109484234 | TTTAGGTAAATGAGT[-/A]AAAAAAAACATATAT | 89910 |
rs148594038 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBE3B | GRCh38.p7 | 12:109511840 | CTTGGCTGCAGCGTG[A/G]AGGGCTGGCTAGAGG | 89910 |
rs148603370 | snp | A/C | 0.0162398 | 0.0886349 | intron-variant | UBE3B | GRCh38.p7 | 12:109521702 | AAGGTTTGTTGTACA[A/C]CAGTGCTAGGTACTT | 89910 |
rs148696226 | snp | C/T | 4.94743e-05 | 0.0049734 | missense, utr-variant-5-prime, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109483877 | AGAGAGATTGATGAC[C/T]TTTTTAAAGCAGATG | 89910 |
rs148729825 | snp | C/G/T | 0.000164804 | 0.00907623 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109533487 | ACCAGCTGCTCCAGA[C/G/T]CCCCGCTCCTGGGAT | 89910 |
rs148742590 | snp | A/G | 1.65203e-05 | 0.002874 | intron-variant | UBE3B | GRCh38.p7 | 12:109501331 | CCTGGCCCTGCATCA[A/G]ATGGAACTGACAGAC | 89910 |
rs148752717 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109542269 | CTGTGTCTTCATGTG[C/T]TGCTTTCAGCAGTCC | 89910 |
rs148947166 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109486386 | TGGCACTGGACCTAA[C/T]TAATAGGTCCAGTTC | 89910 |
rs148967154 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | UBE3B | GRCh38.p7 | 12:109519426 | TTAAACAAAGAGGCT[A/G]GTGTGGAGCTGATCA | 89910 |
rs148983034 | snp | A/G | 0.0376037 | 0.131863 | intron-variant | UBE3B | GRCh38.p7 | 12:109504823 | TTTTTTTTTTTTTTC[A/G]AGACGGAGTCTCACT | 89910 |
rs149140692 | snp | A/G | 0.0158469 | 0.0875917 | utr-variant-3-prime, intron-variant | UBE3B | GRCh38.p7 | 12:109535451 | CTGCGTCCTCAGCGG[A/G]CTGAGCTGCCAGAGA | 89910 |
rs149176256 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-5-prime, intron-variant, upstream-variant-2KB, nc-transcript-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109477949 | GGGGCTCTTTCCGCG[A/G]CCCTTTCCACCTCTT | 89910 |
rs149194298 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109539815 | CTCCCTGTGTGCCCA[C/T]ACCCCAGCTATTCCC | 89910 |
rs149239982 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | UBE3B | GRCh38.p7 | 12:109495695 | TAACTAAAAGTATTC[C/T]TTATGGGGAAACAAA | 89910 |
rs149249654 | snp | C/T | 0.0189856 | 0.0955633 | utr-variant-3-prime, intron-variant | UBE3B | GRCh38.p7 | 12:109536592 | ACTGGTGTTCACTGA[C/T]ACCTTGATGGCTCTT | 89910 |
rs149355888 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | UBE3B | GRCh38.p7 | 12:109511752 | AGGCTGGGAGCAAGG[C/G]CTTTCTGCAAAGCCA | 89910 |
rs149397843 | snp | C/T | 6.59489e-05 | 0.00574196 | intron-variant | UBE3B | GRCh38.p7 | 12:109488536 | TCTGGAATCAGAAGA[C/T]GTGTGTCTTAATCTT | 89910 |
rs149453671 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | UBE3B | GRCh38.p7 | 12:109533388 | AGACAGAGCAAACAC[A/G]TGCTACACAGCTGCA | 89910 |
rs149472470 | snp | C/T | 0.0010544 | 0.0229366 | synonymous-codon, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109521156 | TTGGCAGGACGGCTA[C/T]GAGCAGCTTAGGCAG | 89910 |
rs149485673 | snp | C/T | 0.000124977 | 0.00790397 | synonymous-codon, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109510387 | GTTCCAGTCTGTCCA[C/T]GGGTGGCTTATGGTG | 89910 |
rs149493092 | in-del | -/C | 0.268452 | 0.249318 | intron-variant | UBE3B | GRCh38.p7 | 12:109523679 | GAGAGGCTGGTGCTG[-/C]CCCCCCACTGACAGG | 89910 |
rs149514611 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | UBE3B | GRCh38.p7 | 12:109506509 | GCTGGCCACCACGCC[C/T]GGCTGATTTTGTATT | 89910 |
rs149628068 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | UBE3B | GRCh38.p7 | 12:109516339 | ACCACACCCAGCTAA[G/T]TTTTGTATTTTGTAT | 89910 |
rs149652395 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | UBE3B | GRCh38.p7 | 12:109482806 | TTCAGAAAAGCACCC[A/G]TTAGTGGACAGGACC | 89910 |
rs149680270 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | UBE3B | GRCh38.p7 | 12:109479806 | CTGGGAGGGCCCCTG[C/G]GAGAAGTGAAAGTTT | 89910 |
rs149682438 | in-del | -/TTTTGT | 0.0810805 | 0.184299 | intron-variant | UBE3B | GRCh38.p7 | 12:109506336 | ACAGACCCAAATCTG[-/TTTTGT]TTTTGTTTTTGTTTT | 89910 |
rs149716805 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | UBE3B | GRCh38.p7 | 12:109530429 | GGCTTTAAGAGAAAT[G/T]AGTAGTGTTCCCCAG | 89910 |
rs149733737 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBE3B | GRCh38.p7 | 12:109485114 | TCCTGCAAATCATAC[A/G]AAAGGTGCCAGTTTG | 89910 |
rs149769171 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | UBE3B | GRCh38.p7 | 12:109498084 | TGTGTTAGTAGCCCA[A/G]AGAAGTGGGTTCTTG | 89910 |
rs149779332 | snp | A/G/T | 0.00557542 | 0.0525036 | intron-variant | UBE3B | GRCh38.p7 | 12:109538790 | CTCATCCACACTGCC[A/G/T]CCTCTGAGGAATCGT | 89910 |
rs149833284 | snp | C/T | 0.00119737 | 0.0244387 | downstream-variant-500B | UBE3B | GRCh38.p7 | 12:109543906 | TAAGGAGGGTTGGAG[C/T]GGGCCTCTCAAAGCA | 89910 |
rs149885870 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | UBE3B | GRCh38.p7 | 12:109514127 | CACTTCATTTTCTGC[A/G]CCCTCTTACATCGCT | 89910 |
rs149927435 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant, utr-variant-5-prime, downstream-variant-500B | UBE3B | GRCh38.p7 | 12:109490923 | TGTAGGTACAAGCCA[C/T]CATGCCTGGCTCACA | 89910 |
rs149953168 | snp | C/T | 0.000270471 | 0.0116259 | missense, utr-variant-5-prime, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109483687 | CGGAGTTTTCTCTGT[C/T]GGAGTCGACTGCAGA | 89910 |
rs149981834 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime, intron-variant | UBE3B | GRCh38.p7 | 12:109535323 | CAGACAGCCAGGCCC[A/G]TCTGCTGCCCAGGGA | 89910 |
rs150042339 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | UBE3B | GRCh38.p7 | 12:109509002 | GAATTAAGAAAGTGT[C/G]ACAGTCAGATCCTTA | 89910 |
rs150115343 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, intron-variant | UBE3B | GRCh38.p7 | 12:109536323 | GATTTCTTCTGAACG[C/T]GTGTGCGCACGCTGG | 89910 |
rs150120989 | snp | C/T | 0.000153988 | 0.00877328 | synonymous-codon, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109524109 | TAAAAACCTCACCTC[C/T]ATCAAGGTGAGCATG | 89910 |
rs150147421 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109476456 | AGGGACAATGAGCTA[C/T]TCAGGGAACAGACCC | 89910 |
rs150209363 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | UBE3B | GRCh38.p7 | 12:109482117 | ATTAAATGCCTTTCA[A/G]TAACACGTAATTAAT | 89910 |
rs150249985 | snp | A/G | 3.35458e-05 | 0.00409534 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109486569 | TGATTTTCTCAAGCA[A/G]CTCAAGGTAACAAAA | 89910 |
rs150261387 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3B | GRCh38.p7 | 12:109487926 | CCTGCTATAGGGTCT[A/G]TGGGCCTAGAAAGCA | 89910 |
rs150271374 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | UBE3B | GRCh38.p7 | 12:109532298 | ATGCTCGTCACAGTG[C/T]GGAAACACAAAAATG | 89910 |
rs150323950 | snp | C/T | 0.000151906 | 0.00871379 | synonymous-codon, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109499640 | CTCTGTAGGCAACCT[C/T]CTACACTTGGGCTCC | 89910 |
rs150376775 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109506207 | GAGGTAAGTGGGGGG[A/G]AGCTTTGCCAAAGGT | 89910 |
rs150419742 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109524783 | TGGCTTTTCGTTACC[A/C]TGGTGAGGATTAGCC | 89910 |
rs150468651 | in-del | -/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109507981 | AGTACCACTGGCTGT[-/G]GGCTTGGGGTCTCCT | 89910 |
rs150474221 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109528338 | AGTAAAGTGGAGCAG[C/T]ACTCGTCACCTGCTT | 89910 |
rs150529761 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBE3B | GRCh38.p7 | 12:109525842 | AGCAAAAGATGAAAA[C/T]GCAAGCTGCCCGTAA | 89910 |
rs150583447 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | UBE3B | GRCh38.p7 | 12:109530287 | GGACTGGGGGTTCTC[C/T]GAAGCTCTAGGAGAT | 89910 |
rs150616667 | snp | G/T | 3.29576e-05 | 0.00405928 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109516803 | GGTTACCAAGGAGAA[G/T]GAGAAACTGGGGCTG | 89910 |
rs150677233 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant, upstream-variant-2KB | UBE3B, KCTD10 | GRCh38.p7 | 12:109479101 | TCTTCTCATAGGACT[C/T]CTCTCCTTATTAGAT | 89910 |
rs150801081 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant, utr-variant-3-prime | UBE3B | GRCh38.p7 | 12:109534233 | CCGGCCACAGCACCG[G/T]TGAGGAGGGAGGAGT | 89910 |
rs150853934 | snp | A/T | 0.000399281 | 0.0141238 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109501438 | GTGCCTCTGATCCGG[A/T]TCTTCTTCTGTGACA | 89910 |
rs150941198 | snp | A/G | 4.94417e-05 | 0.00497176 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109523993 | GGAATTGTGGTGGAC[A/G]TGCCATTTGCATCCT | 89910 |
rs150944416 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | UBE3B | GRCh38.p7 | 12:109517268 | GACTCTCAACTGTGA[C/T]TGTAGTATATAAGTG | 89910 |
rs150962720 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBE3B | GRCh38.p7 | 12:109505241 | AATACTGCTGTTTTT[C/T]TACTGACAACTTAGG | 89910 |
rs150971562 | snp | C/T | 0.0105526 | 0.0718675 | synonymous-codon, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109524043 | TGGGCACCACCACAG[C/T]GTCTTCTATAGCTCG | 89910 |
rs151059374 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | UBE3B | GRCh38.p7 | 12:109526786 | TGAGGCAGGAGAATC[G/T]CTTGAACCTGGGAGG | 89910 |
rs151084567 | snp | C/T | 0.000181271 | 0.00951855 | missense, utr-variant-5-prime, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109486504 | GCTTGTTCTAAGGAC[C/T]TCACCCTCCTTTGGA | 89910 |
rs151113180 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109531891 | CCCCACAAAACAGGT[A/G]TGTTTGTGCCTTTGG | 89910 |
rs151121249 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3B | GRCh38.p7 | 12:109543330 | ACCAGGTGCCAGAAA[C/T]CAGCCTCATGCAGAC | 89910 |
rs151175581 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109540139 | GTCTTCTGCTCCTTG[C/G]CTGCCCCAGGCCCTG | 89910 |
rs151208600 | snp | A/G | 0.00636936 | 0.0560724 | utr-variant-5-prime, intron-variant, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109481682 | GCTGTTCTCAGCCAC[A/G]AGTCCTGTGCAAGAT | 89910 |
rs151302892 | snp | A/G | 0.000153988 | 0.00877328 | synonymous-codon, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109501470 | CCTGAGCAAGAAGCT[A/G]CTGGAGAGCCAGGAG | 89910 |
rs151321825 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | UBE3B | GRCh38.p7 | 12:109494242 | GGCTATTTAACTCCA[G/T]AACTCATACTCTTTC | 89910 |
rs151329540 | snp | A/T | 0.000585662 | 0.0171023 | intron-variant | UBE3B | GRCh38.p7 | 12:109507533 | GGTGGAGTCTCCACC[A/T]GAAGCTTGGGTTTCT | 89910 |
rs180670925 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109516586 | TATTTCTAATTCCCA[C/T]AAGTGTTCCAGGGAA | 89910 |
rs180684614 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant, downstream-variant-500B | UBE3B | GRCh38.p7 | 12:109536922 | TTTCAGATGAGCACC[C/T]TCTATGGGCCCATCC | 89910 |
rs180686260 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109494623 | TTTGTCACCCAGAGG[C/T]ACTTAAATGCAACAG | 89910 |
rs180761449 | snp | G/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109475672 | AGCTTTATCTAAGAG[G/T]TGCCAGGGATGTGAG | 89910 |
rs180762690 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE3B | GRCh38.p7 | 12:109525999 | TTTTTAGTAAACGCA[C/T]ATTTTCATCATATTG | 89910 |
rs180772448 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109485729 | TTTGCCAGATTGATA[C/G]TGTTTTTTGAAAGAA | 89910 |
rs180936474 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE3B | GRCh38.p7 | 12:109480565 | CTGAGGTGGGAGAAT[C/T]GCTTGAGCCTGGGAG | 89910 |
rs180979906 | snp | A/G | 3.47162e-05 | 0.00416616 | synonymous-codon, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109521464 | TGGGGATGAGAGGCT[A/G]TACCCCTCACCCACA | 89910 |
rs180999569 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBE3B | GRCh38.p7 | 12:109490242 | TTTGGCTGCAAGGGT[A/G]ATCCAGTCTTTTGAC | 89910 |
rs181000807 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109539988 | GTCTGTGTCAGCTTA[A/T]AGACCTTCCACCGAG | 89910 |
rs181078515 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109532251 | CGACACACAGCATCC[A/G]TAGAGTGATTGGATG | 89910 |
rs181081068 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109508808 | ATGGCTCATTTATTC[A/G]TATGTTCTTTCAAAC | 89910 |
rs181108217 | snp | G/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109494377 | CCCTGTTCCTCACAC[G/T]GCCGTGGCATTGATT | 89910 |
rs181150030 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | UBE3B | GRCh38.p7 | 12:109515415 | ACTCTTGTTGCCCAG[A/G]CTGGAGTGTGATGGT | 89910 |
rs181237393 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | UBE3B | GRCh38.p7 | 12:109504883 | AATCTCGGCTCAACT[G/T]CAGGCTCCGCCTCCC | 89910 |
rs181246312 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | UBE3B | GRCh38.p7 | 12:109536221 | AAGGAATTTAAAGAC[A/G]GGAATGTATTAATAT | 89910 |
rs181337349 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109527155 | GATGAATTCAAATGC[C/G]ACAGACGGAGGTCCT | 89910 |
rs181461089 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3B | GRCh38.p7 | 12:109541673 | GGTGGCTTAAAACAA[C/T]GGAAATGTATTCTCC | 89910 |
rs181469869 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109523158 | GGTCCTCTGACAGGT[A/G]TCATCAAGTCCGAGT | 89910 |
rs181480815 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109508616 | AGGATCAGGGACATG[C/T]AGGTGGCAGATTGGG | 89910 |
rs181605733 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109531867 | TGTCTCATCATTGTG[C/T]AGGTGCTGCCCCACA | 89910 |
rs181674075 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109489508 | ATTTCAGGCATGACC[C/T]TGGCCTCTTGGGGGG | 89910 |
rs181725590 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE3B | GRCh38.p7 | 12:109504214 | TGTCTTGTGTGTTTT[A/G]GGATGTTTAGCAGCC | 89910 |
rs181740409 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3B | GRCh38.p7 | 12:109485825 | CTCTTGGGCCACCAG[C/T]TGGAGAACCCTTTAG | 89910 |
rs181756013 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109526958 | GAGGCACCCAGGCCA[C/T]GGTGTTCTTAGGAGT | 89910 |
rs181842656 | snp | G/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109488972 | ATTCACTTAAGCCTT[G/T]TCATTTTACTTGGAA | 89910 |
rs181847653 | snp | A/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109508228 | AAAAGACATAATTAT[A/T]GCAAAGTGCTTATCA | 89910 |
rs181981505 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3B | GRCh38.p7 | 12:109480124 | GTGAGAAATGTCAGA[C/T]TGCCAGCATTATTTC | 89910 |
rs182029882 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109522655 | CTCAGGGCCAAACTC[C/G]TTTCACTCTCGAATA | 89910 |
rs182041631 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109482279 | AGGGCACCCATCACC[C/T]GAATGGTGAACATTG | 89910 |
rs182049879 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109486301 | TTACTAGGCTATTTT[G/T]TCTTTGCGTTTAGTG | 89910 |
rs182252219 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109539007 | TTGGGAGGCTGAGGC[A/G]GGCAGATCCCCTGAG | 89910 |
rs182265174 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109519232 | ATAGAGCTGGGCCTG[A/G]AAGCCAGGCATCCCT | 89910 |
rs182329731 | snp | A/G | 8.23757e-05 | 0.00641725 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109498267 | CCCATGACATGCTTC[A/G]TAAATTCATCATATT | 89910 |
rs182369171 | snp | A/C | | | upstream-variant-2KB, intron-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109475884 | AGCTACCGCCAATTG[A/C]AACTTCCATCAAATG | 89910 |
rs182393406 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109506002 | CTTTCTAAGTCAAGA[A/G]ATGTGTTATTAGATG | 89910 |
rs182395476 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109512229 | ATCAGACAGCACCCA[A/G]GTCTGCTGACTCCCC | 89910 |
rs182400134 | snp | A/G | 0.00398564 | 0.0444627 | utr-variant-5-prime, intron-variant, upstream-variant-2KB, nc-transcript-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109477933 | TGGCGTGTGTGCTCC[A/G]GGGGCTCTTTCCGCG | 89910 |
rs182403855 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE3B | GRCh38.p7 | 12:109523786 | GTGTCCTGACCACTG[C/T]GCTGTCCCCAGGAGG | 89910 |
rs182408727 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBE3B | GRCh38.p7 | 12:109492506 | CAGCACTTTGGGAGA[C/T]TGAGGTGGGCAGATC | 89910 |
rs182410078 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109542764 | ACAGATTCTCCTTCA[C/T]AGCCTGGAGAGGAAC | 89910 |
rs182416909 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, missense | UBE3B | GRCh38.p7 | 12:109533987 | TTCATTTCCTCATTG[A/G]CCAAAGGAGAAGGAA | 89910 |
rs182446252 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109540628 | CTTGTCGGAATGGCA[A/C]ATGGATGTTTAAAAA | 89910 |
rs182641450 | snp | C/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109495665 | TGATAAGCATTGTTT[C/G]TATAGATTATAGATT | 89910 |
rs182657703 | snp | C/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109527466 | GGCTCAGTCCCACCT[C/G]GTGAGTCATTTGAAT | 89910 |
rs182721100 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109495263 | AGAGCCTAAATACCA[C/T]TAACACCTCTGCTCA | 89910 |
rs182727361 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3B | GRCh38.p7 | 12:109518210 | AAAAATAGCCCCCAC[A/G]AGTGAGTTGATAAAT | 89910 |
rs182746871 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109538504 | AGGAATCTTGATGTC[C/G]CCTCCAGAGCACGTG | 89910 |
rs182753636 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109499301 | AACTAAATATCACCT[A/G]CCTCTGTGTGCCTAA | 89910 |
rs182833950 | snp | G/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109507232 | CTGACATACAGGCTG[G/T]GTGATTTGGGGCCAA | 89910 |
rs182859051 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | UBE3B | GRCh38.p7 | 12:109498699 | GCTTATATCAGAGCA[C/G]CGCCTGCTTTACCTA | 89910 |
rs182873254 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | UBE3B | GRCh38.p7 | 12:109482959 | ACCTTTTGCTTTGTT[A/T]ATGTTGAAATGGCCC | 89910 |
rs182974823 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UBE3B | GRCh38.p7 | 12:109528018 | GCTGCTAAGTAGAGC[A/G]CCCAGAGGAGGTAGG | 89910 |
rs182990185 | snp | A/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109506918 | ATTAGACCACATTCA[A/T]ATAAGGCAAAGCCGA | 89910 |
rs183026049 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109484136 | ACCTGTTTTGGAGGG[A/G]TTATGCCCAGTGCTT | 89910 |
rs183048354 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109487026 | TCTCCCTCTCATTCT[C/T]TTCTCTCATCCCTGC | 89910 |
rs183209279 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109504583 | TGTGTTGTGGCTGTG[A/G]CAAGGGAAAGGGGCC | 89910 |
rs183250703 | snp | A/G | 4.97797e-05 | 0.00498873 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109511220 | GATCTCAAACCTAGC[A/G]TGCTCTTCCAAGAAC | 89910 |
rs183332870 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3B | GRCh38.p7 | 12:109491375 | TTTGGAAACTATTCA[A/G]AATGAATTTCTTTTA | 89910 |
rs183337462 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBE3B | GRCh38.p7 | 12:109533071 | GTCTCCCATTTTCTC[C/T]TCACATGGTCTCTCT | 89910 |
rs183341481 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant, downstream-variant-500B | UBE3B | GRCh38.p7 | 12:109509962 | TCGAGGATTATTAAT[C/G]ATGATTAATTTTGCC | 89910 |
rs183496572 | snp | A/G | 0.000379153 | 0.0137635 | intron-variant | UBE3B | GRCh38.p7 | 12:109533437 | GCAGGAGCCTGCCCC[A/G]TCCCCACTGACCCTG | 89910 |
rs183505316 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3B | GRCh38.p7 | 12:109491875 | GACCCCATGGGCTTA[C/T]TTAACCCGGGGTTGG | 89910 |
rs183553019 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109538155 | AATAATTAGCTGGAA[C/T]AGAGTTTGAGAAGCG | 89910 |
rs183559341 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109540061 | TCTCTGAAGATGTGC[C/T]CTGCCTCCTTGACCC | 89910 |
rs183742538 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | UBE3B | GRCh38.p7 | 12:109507893 | ACCAAGTGAGCAGTG[C/T]GCAGTAAATGTTCAG | 89910 |
rs183755079 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109488381 | TCCATTATCAGGCAC[C/T]AGAGTGCCACATTCC | 89910 |
rs183839985 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE3B | GRCh38.p7 | 12:109517486 | CAGAAAATTGTCACA[A/G]TACATTGGTTTTGTT | 89910 |
rs183850919 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109476198 | TTGAATAAGTTACCA[G/T]GTGTTGCTGCTGGTG | 89910 |
rs183990347 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3B | GRCh38.p7 | 12:109524367 | CAAAGCAGCGCCTCA[A/G]GGGAGGGTTAAACCT | 89910 |
rs183998581 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | UBE3B | GRCh38.p7 | 12:109539539 | CCTGCAGTTTCCTCT[A/T]CCATGAAACGAGGAT | 89910 |
rs183998622 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109497241 | TATCTGTCCTCAATC[C/T]TTTAAAAATGTATCT | 89910 |
rs184005960 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109520430 | TGAGGTCTGGATGGA[A/G]TAGATGTGCTGAATG | 89910 |
rs184132135 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109501874 | TTACCTTATTGCCCA[A/G]GTTTGTTTCCAATTC | 89910 |
rs184150171 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | UBE3B | GRCh38.p7 | 12:109544061 | GGTGTGTTTGGGAAG[C/T]AGCTGCCCACAGCTC | 89910 |
rs184194650 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3B | GRCh38.p7 | 12:109485207 | GTAATAGTACTAACA[A/G]TGCCACTGAGGCATG | 89910 |
rs184291791 | snp | C/T | 0.000181517 | 0.00952499 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109524472 | CTGACCTGGGCCTGA[C/T]GCTGTCTTACGACGA | 89910 |
rs184303746 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | UBE3B | GRCh38.p7 | 12:109502504 | GAGTGTGTTGCAAAA[C/T]TCTGTCTCATAGCTA | 89910 |
rs184463990 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBE3B | GRCh38.p7 | 12:109529771 | TGATGAAACACTCTG[A/G]TACTATTTGTGTTTT | 89910 |
rs184501627 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109503557 | CTGTGCCTGAGTGTA[A/C]TGCACATATAAAATA | 89910 |
rs184542040 | snp | C/T | | | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109477502 | TGGGGAGGGCATTTA[C/T]CCCACCTCCGCTATT | 89910 |
rs184612745 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109524799 | TGGTGAGGATTAGCC[A/G]TTACAAATGGAGGAT | 89910 |
rs184622460 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBE3B | GRCh38.p7 | 12:109485370 | GCCCAGCAAGAGAGG[A/G]AGGACTATGCAGGCA | 89910 |
rs184656260 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109488973 | TTCACTTAAGCCTTG[C/T]CATTTTACTTGGAAA | 89910 |
rs184663987 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBE3B | GRCh38.p7 | 12:109508362 | TAGAATGAAGAGAAT[A/G]TTACCAGTTCAATAG | 89910 |
rs184768545 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE3B | GRCh38.p7 | 12:109530843 | GGGGCTTGAGGGGCA[C/T]GGCCGAGCCTGCTGT | 89910 |
rs184861651 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109528504 | TATTTGGACTCTACT[C/G]ATTTGGAATTGGTGA | 89910 |
rs184868169 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3B | GRCh38.p7 | 12:109487408 | AGCTCAGTAATGGAA[C/T]GAAAGTCCCCAGACC | 89910 |
rs184917284 | snp | C/T | 0.00478085 | 0.0486577 | utr-variant-3-prime, intron-variant | UBE3B | GRCh38.p7 | 12:109535347 | CCAGGGAAGCGCAGG[C/T]GCCTGCTAGGGACGC | 89910 |
rs184927446 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | UBE3B | GRCh38.p7 | 12:109513630 | TGAATAAGAAAGTCA[A/G]GGAACCGCTGAGATA | 89910 |
rs184935835 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109485744 | CTGTTTTTTGAAAGA[A/G]GCCTCAATTTGGGTT | 89910 |
rs184959734 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109507162 | CCTGAAACAAATTGC[C/T]GATCCCTGATTTAAA | 89910 |
rs184991828 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109494064 | CTCCTGGCCTCAAGC[A/G]ATCCTCATGCCTCAG | 89910 |
rs185000661 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109509035 | AATAAGAAAAATATA[C/G]AGTACAGATTTTTTC | 89910 |
rs185002820 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109532677 | TAGCACATTTGCAGG[A/G]ATAACGCAGGGGCTG | 89910 |
rs185064031 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109490392 | GTGCCAGATCATACC[C/T]CTAGGGAATTGTTGA | 89910 |
rs185164846 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109515004 | CTGCAAGCTCCACCT[A/G]CCGGGTTCACGCCAT | 89910 |
rs185197165 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | KCTD10, UBE3B | GRCh38.p7 | 12:109475457 | ACTCTCCAGCCTGGG[C/T]GACAGAGCAAGACCC | 89910 |
rs185239425 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109494313 | TTGTATTCTAAGAAT[A/G]ATATATATATTTTTT | 89910 |
rs185279378 | snp | A/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109496297 | TGGATATACCACATT[A/T]GAGTTGTTTCTACTT | 89910 |
rs185284114 | snp | A/C | 0.00358779 | 0.0422022 | utr-variant-3-prime, intron-variant | UBE3B | GRCh38.p7 | 12:109535712 | TCACTCCTGAGTCTG[A/C]AAAATCCCAGGAAAC | 89910 |
rs185313995 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | UBE3B | GRCh38.p7 | 12:109539295 | GGCGGCATTCATAGT[A/T]CTCACCACCCTCTGG | 89910 |
rs185333931 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109494414 | ACGCCTAGTTTGCCC[A/C]GGCACTTAGTCATGT | 89910 |
rs185339174 | snp | A/G | 0.0023933 | 0.0345097 | utr-variant-3-prime, intron-variant | UBE3B | GRCh38.p7 | 12:109536664 | AACTTATGGATTGAG[A/G]TGTGATCAAAGGCTT | 89910 |
rs185342768 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109515727 | GGAGATTCCCATTTT[A/T]AAAAAAACAGCTGTG | 89910 |
rs185361641 | snp | A/C | | | intron-variant | UBE3B | GRCh38.p7 | 12:109486580 | AGCAGCTCAAGGTAA[A/C]AAAAAAAAAAAAAAA | 89910 |
rs185390871 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBE3B, KCTD10 | GRCh38.p7 | 12:109479216 | CTAATCTTTCTACCT[A/G]TATGATTCTTGTTTC | 89910 |
rs185434163 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109520234 | CTGGGCCCTGTGCTG[C/T]TCAGCACTGTTTTTA | 89910 |
rs185566351 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109526473 | GACTTCATTCTGGCT[C/T]TCTGCGCTTATGTTG | 89910 |
rs185691873 | snp | C/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109503803 | TTGTTATGAATTGGT[C/G]TTACAAGTACAAAAG | 89910 |
rs185731690 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109498821 | TTTAGATAGGAAAAG[A/T]TTTTTTTGTTTTTTT | 89910 |
rs185751085 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | UBE3B | GRCh38.p7 | 12:109482971 | GTTAATGTTGAAATG[G/T]CCCTTTCTTTTTTGT | 89910 |
rs185805821 | snp | C/T | | | intron-variant, upstream-variant-2KB | KCTD10, UBE3B | GRCh38.p7 | 12:109475539 | ACACCCCAGATCAAT[C/T]AATCAGTATCTCAGA | 89910 |
rs185848489 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | UBE3B | GRCh38.p7 | 12:109542072 | AACTGTCTTCCAGAG[C/G]AAGTGTGGCAGGAGG | 89910 |
rs185860681 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109523246 | CCCTGGCACAGTCTG[C/T]CGGCGTTTTCCCCTG | 89910 |
rs185914229 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3B | GRCh38.p7 | 12:109481895 | CAATTACTTTTGTAC[C/T]AACCTAATACCTTCC | 89910 |
rs185932867 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UBE3B | GRCh38.p7 | 12:109521926 | CATGAGGAGTGGTGT[A/G]CAGAGCCAGATGGCC | 89910 |
rs186012856 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBE3B | GRCh38.p7 | 12:109527024 | GAGCCATTCAGCACA[C/T]TGTCCTGAACCCAGA | 89910 |
rs186076221 | snp | A/C | 0.00755907 | 0.0610114 | intron-variant | UBE3B | GRCh38.p7 | 12:109504691 | TAGGGCAGGTTTCCC[A/C]AAGATGAGCAGAGGG | 89910 |
rs186078672 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109498042 | CTTTAATTGTTCTTT[A/G]GGACCAGTGGCCGTG | 89910 |
rs186087654 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | UBE3B | GRCh38.p7 | 12:109480212 | TTTTTTTTAATCCTT[G/T]TGTCTATAAAAATAA | 89910 |
rs186092510 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109485935 | ACGTGCCAGGTACCC[A/G]CTGAAGGCTTGTTTT | 89910 |
rs186095674 | snp | A/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109512929 | CTGTTCTGTGGCTTT[A/T]CTTTTCCAAAAGATA | 89910 |
rs186148953 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109533224 | TGCTCTCACAAGTGG[A/C]CAGTCGCACCTATTG | 89910 |
rs186156942 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | UBE3B | GRCh38.p7 | 12:109510050 | GCACACTTGAGATGA[C/G]AGTCCACCTCCCGAA | 89910 |
rs186241501 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109505780 | TTCACCCTCTAAGTA[C/T]CCTTCAGTAGCTCTG | 89910 |
rs186298224 | snp | A/G | | | intron-variant, downstream-variant-500B | UBE3B | GRCh38.p7 | 12:109536964 | TTCCCAGAGGCAGCT[A/G]TCACCATAGGTTGGG | 89910 |
rs186324240 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109482804 | TCTTCAGAAAAGCAC[C/T]CGTTAGTGGACAGGA | 89910 |
rs186356872 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109489716 | CAAGAGGTGACACTT[A/G]AGCCAGGCCTACCAG | 89910 |
rs186359731 | snp | A/G/T | 0.000988739 | 0.0222161 | intron-variant | UBE3B | GRCh38.p7 | 12:109486123 | CTTAAGGGCCAACCT[A/G/T]CTGGGCTCTGAAAGT | 89910 |
rs186372235 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3B | GRCh38.p7 | 12:109532150 | ACCTGAATTTGCAGC[A/G]GGCAGACCTGAGCCG | 89910 |
rs186413403 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109527248 | CAGAATCTATCATAA[A/G]TGTCATCCTTTTTGG | 89910 |
rs186599325 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109508617 | GGATCAGGGACATGT[A/G]GGTGGCAGATTGGGT | 89910 |
rs186652915 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBE3B | GRCh38.p7 | 12:109517811 | GTATGTGGCCAGATA[C/G]CCACCCCCACCAGCA | 89910 |
rs186670967 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109476403 | ACAAGCAAGCAAGTA[C/G]AAAGAAGATCTGGGC | 89910 |
rs186723579 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109492982 | ACATATAGCCAGTGG[C/T]TACCATATTAGACCA | 89910 |
rs186731336 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UBE3B | GRCh38.p7 | 12:109512343 | ACAGAGGGCCAACAC[A/G]AGGAGGGAAGGAGGG | 89910 |
rs186888312 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBE3B | GRCh38.p7 | 12:109495113 | ACTCAGATCAGAGAG[A/G]TTAGCTCAGTTGGTT | 89910 |
rs186898782 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109538156 | ATAATTAGCTGGAAC[A/G]GAGTTTGAGAAGCGC | 89910 |
rs186985771 | snp | A/G | 0.0402882 | 0.136092 | intron-variant | UBE3B | GRCh38.p7 | 12:109538623 | CTTTCACTTTAAGAA[A/G]ACAGGGCTGCCCATG | 89910 |
rs187031506 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109498586 | GAACATTAGATGTCA[A/G]CCTTTAGCTTCCTGG | 89910 |
rs187058305 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | UBE3B | GRCh38.p7 | 12:109495355 | TACCTTTTTTTCTGC[A/G]TGACCTCTGAGTGAT | 89910 |
rs187062814 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109518338 | GACGAGGTGGGCTCC[A/G]TAACGCTCTTGAGTT | 89910 |
rs187067201 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109540673 | AAACCCAGTGTCCTT[A/G]GCCTTCAGACCACGG | 89910 |
rs187071131 | snp | A/G | 0.0023933 | 0.0345097 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109477570 | TCCTTCCCGGGCGAA[A/G]AAGCTCTGCGGAACT | 89910 |
rs187163061 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBE3B | GRCh38.p7 | 12:109485269 | CATTCCTATTGCTAA[A/G]CTTCACATTGTGCCA | 89910 |
rs187177234 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBE3B | GRCh38.p7 | 12:109524714 | CCTTTGAAGCTTCCC[A/G]CAGAGACCCTGCTTT | 89910 |
rs187190433 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109502623 | TGTCAGAACTAGAGG[C/T]TGTCACGCCTTACTT | 89910 |
rs187217819 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | UBE3B | GRCh38.p7 | 12:109494638 | TACTTAAATGCAACA[C/G]CTACAGGTAGGCTAA | 89910 |
rs187240973 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | UBE3B | GRCh38.p7 | 12:109522990 | CTGGAAAGCATGGCC[G/T]CCTGGCTTCTCTGAA | 89910 |
rs187308913 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109528236 | CTTGCACTTTATGAG[C/T]GTTGGATGTTTCCCA | 89910 |
rs187321189 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | UBE3B | GRCh38.p7 | 12:109506931 | CAAATAAGGCAAAGC[C/G]GAGGTGTAACCAGTC | 89910 |
rs187390178 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109475957 | TCTCTCAATGTTCTA[A/G]TGAGAAAGATGTTTA | 89910 |
rs187402288 | snp | C/T | | | upstream-variant-2KB, intron-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109476772 | TGGAAACTCAGCGAC[C/T]CCAGCCACAACCTCC | 89910 |
rs187523553 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109484247 | AGTAAAAAAAACATA[C/T]ATGAGATAAAACATA | 89910 |
rs187549044 | snp | A/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109502164 | GAACTTCAGTTTGGC[A/T]GTGAACCAACATGAA | 89910 |
rs187552571 | snp | C/T | 1.64732e-05 | 0.0028699 | synonymous-codon, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109524040 | GCTTGGGCACCACCA[C/T]AGCGTCTTCTATAGC | 89910 |
rs187635513 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE3B | GRCh38.p7 | 12:109484485 | CAGTCTTCACCTCCC[A/G]GGTTCAAGCAGTTCT | 89910 |
rs187779834 | snp | A/G | 0.0019486 | 0.0311529 | intron-variant | UBE3B | GRCh38.p7 | 12:109499587 | GGGCCGGGAGGCACC[A/G]AAATGTTTGTCTGGG | 89910 |
rs187786524 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109507281 | CTTCAGTTTCCTCCT[A/G]TATAAGATGGGGATA | 89910 |
rs187787449 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109486414 | TTCCAACAGTTAGAG[C/G]ACAAGTGATATGATC | 89910 |
rs187815293 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3B | GRCh38.p7 | 12:109543174 | TTCAGGCCTCGGGAA[A/G]TACAGAAGGGCTGCG | 89910 |
rs187906865 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBE3B | GRCh38.p7 | 12:109527470 | CAGTCCCACCTGGTG[A/C]GTCATTTGAATCAGA | 89910 |
rs187921191 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109506400 | GTCGCCCAGGCTAGA[A/G]TGCAGTGGTGCGATC | 89910 |
rs187968098 | snp | C/T | 0.00546885 | 0.052005 | intron-variant | UBE3B | GRCh38.p7 | 12:109499839 | GCAAATCACTGTCTT[C/T]CCTGCCTCTCTCCCA | 89910 |
rs188076017 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109529107 | CAGAGGTCGCAGTGA[A/G]CTGAGATCGCACCAC | 89910 |
rs188080323 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | UBE3B | GRCh38.p7 | 12:109487949 | AGAAAGCAGTCAGGC[C/T]TTTTGCTTGACTTAC | 89910 |
rs188087942 | snp | G/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109507240 | CAGGCTGTGTGATTT[G/T]GGGCCAATTATTTAA | 89910 |
rs188146584 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109492132 | TACACAAATGAGCAT[G/T]ACTGTGTTCCAGTAA | 89910 |
rs188162376 | snp | C/G | 0.000174383 | 0.00933601 | intron-variant | UBE3B | GRCh38.p7 | 12:109533773 | CCCTCTCTCGGCAGC[C/G]CCTTTCTCTTTCCTT | 89910 |
rs188213591 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109475671 | CAGCTTTATCTAAGA[A/G]TTGCCAGGGATGTGA | 89910 |
rs188240872 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBE3B | GRCh38.p7 | 12:109494460 | CTTCTGTTTTTCCCC[A/G]TATGCCTGCCCAGCT | 89910 |
rs188245105 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | UBE3B | GRCh38.p7 | 12:109536802 | CCACAATGGAGGGAA[G/T]ATGTGGAGGGGCGCA | 89910 |
rs188251483 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | UBE3B | GRCh38.p7 | 12:109516405 | TGGTTTTGAACTCCC[C/G]ACCTCAGGTAATCCG | 89910 |
rs188315997 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | UBE3B | GRCh38.p7 | 12:109487043 | TCTCTCATCCCTGCT[C/G]CCTTTTGGGGTCACC | 89910 |
rs188362418 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UBE3B | GRCh38.p7 | 12:109480277 | AATGTGCACTCAAGT[A/G]CCTCCATAGGTACCT | 89910 |
rs188375434 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109521026 | CCTGTCATGCATCCA[C/T]GTTTCATAATTTGCA | 89910 |
rs188389346 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBE3B | GRCh38.p7 | 12:109539837 | GCTATTCCCGAGCTT[C/T]CATTATGCACTGGGG | 89910 |
rs188389683 | snp | G/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109497438 | AACACACCTGGGTAA[G/T]CACCACCCAATAGAG | 89910 |
rs188419638 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBE3B | GRCh38.p7 | 12:109511938 | GAGATTTTTAAGGAG[A/G]CCTCAGAGAATGGTC | 89910 |
rs188536609 | snp | A/C | | | intron-variant | UBE3B | GRCh38.p7 | 12:109533324 | TTTGGGGCCAGATCC[A/C]CCCCGCCACTCCATA | 89910 |
rs188867835 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | UBE3B, KCTD10 | GRCh38.p7 | 12:109479233 | ATGATTCTTGTTTCC[C/G]TAACTAGATTGCAAG | 89910 |
rs188880545 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109524378 | CTCAAGGGAGGGTTA[A/G]ACCTCTTAAGCACAT | 89910 |
rs188932409 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE3B | GRCh38.p7 | 12:109496029 | CATAATATTTTATCA[C/T]CCTGAAAAGAAACCT | 89910 |
rs188949938 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109491377 | TGGAAACTATTCAAA[A/T]TGAATTTCTTTTATC | 89910 |
rs188972664 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109539161 | GAATTGCTTGAACCC[A/G]GGAGGCGGAGGTTGC | 89910 |
rs189000817 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109496880 | CACAAAAGTTTTAAA[C/T]TTTGAAGAAGCACAA | 89910 |
rs189150347 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | UBE3B | GRCh38.p7 | 12:109531178 | TCCCAATAAAACACA[A/C]ACAATTGCTTAGGCT | 89910 |
rs189170472 | snp | A/C | | | upstream-variant-2KB, intron-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109477039 | CTTCCCGGATTCCTA[A/C]CCGCCAGGGAGCCTC | 89910 |
rs189229105 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant, upstream-variant-2KB | UBE3B, KCTD10 | GRCh38.p7 | 12:109478121 | TTGGGTGAGTTCCCT[C/T]ACCTCTCTGAGCCTC | 89910 |
rs189230307 | snp | A/G/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109524936 | CCTGGTCTCAGGGCC[A/G/T]CAGCACGTCTCCTCC | 89910 |
rs189234402 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBE3B | GRCh38.p7 | 12:109485509 | ACATGGTTTAAGGGC[A/G]GATCCAGGATTGGTA | 89910 |
rs189248652 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | UBE3B | GRCh38.p7 | 12:109519702 | GTTTAAATGCTGTTA[C/T]AGCTGCCTGTTGACT | 89910 |
rs189297386 | snp | C/T | 0.0146672 | 0.084371 | utr-variant-3-prime, intron-variant | UBE3B | GRCh38.p7 | 12:109535594 | CCAAAGCCTGCTTGT[C/T]CCGCGGAGGACGGCT | 89910 |
rs189297745 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109504060 | CTGAAAATAAGCAAG[G/T]AAAAAGTAGGGCTCA | 89910 |
rs189317169 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109485762 | CTCAATTTGGGTTTT[C/T]ATGTGAAGTATACCA | 89910 |
rs189430695 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109526595 | ATTCAATTTGCGGCC[A/G]GGCACAGTGGCTCAT | 89910 |
rs189459798 | snp | A/C | | | intron-variant | UBE3B | GRCh38.p7 | 12:109499323 | TGTGCCTAACATTTT[A/C]CCTGCCACTTCATCC | 89910 |
rs189579220 | snp | C/T | 1.6492e-05 | 0.00287154 | synonymous-codon, intron-variant | UBE3B | GRCh38.p7 | 12:109530067 | GATTGATCTGGAAGA[C/T]TTAAAGTAAGAGGCG | 89910 |
rs189632288 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3B | GRCh38.p7 | 12:109508061 | GATTCCTGGAAAATT[C/T]CAAAGTCAGAGCCAG | 89910 |
rs189649161 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBE3B | GRCh38.p7 | 12:109488947 | AGTGCCTTAGCCTCC[A/G]AGTGATTACATTCAC | 89910 |
rs189714060 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | UBE3B | GRCh38.p7 | 12:109535910 | CTCCAGGGAACTGAG[A/G]CAGAGGCCCTGTTTG | 89910 |
rs189778940 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109494339 | TTTTTAGTAAATAGC[A/G]CTTGAGAACCTTCCC | 89910 |
rs189796158 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109486604 | AAAAAAAAAAAAAAA[A/G]CAAAACCAGAAACAG | 89910 |
rs189819838 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBE3B | GRCh38.p7 | 12:109532236 | GACTAACCACAGCCC[C/T]GACACACAGCATCCG | 89910 |
rs189965239 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3B | GRCh38.p7 | 12:109515160 | CCTCATGATCCGCCC[A/G]CCTAGGCCTCCCAAA | 89910 |
rs190042776 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109489258 | TAAATAGATGTCGCT[C/T]ATAGATATAAAATGA | 89910 |
rs190059911 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109520249 | TTCAGCACTGTTTTT[A/G]TAGTCACTGCTCTGA | 89910 |
rs190205149 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UBE3B | GRCh38.p7 | 12:109498987 | CACACTACCACGGCC[A/G]ACTAATTTTTGTATT | 89910 |
rs190221585 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE3B | GRCh38.p7 | 12:109542194 | ACGGGAAATATTTGG[C/T]GCCTGTGTCATCACT | 89910 |
rs190226261 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109514560 | TGTAACTCGCCTTCC[A/G]CCTGTGTATCACCAA | 89910 |
rs190237046 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109523398 | TGCAGCAAGGCTTAC[A/G]GGCCCTCCCTGACCT | 89910 |
rs190300905 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109508442 | AGAGTGGGAAATTAA[C/T]AAACATTAGTCCCAT | 89910 |
rs190308709 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109539327 | GCGTGGGGTCAGAAT[A/G]GCATCCTTTGCTTCA | 89910 |
rs190354953 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | UBE3B | GRCh38.p7 | 12:109504880 | CGCAATCTCGGCTCA[A/G]CTGCAGGCTCCGCCT | 89910 |
rs190381349 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109476808 | GCCAAACGCTCCGCC[C/T]CAAGGAATCCTACCT | 89910 |
rs190387817 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE3B | GRCh38.p7 | 12:109527028 | CATTCAGCACACTGT[C/T]CTGAACCCAGAGGGC | 89910 |
rs190392027 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109495255 | GAATTCTGAGAGCCT[A/G]AATACCACTAACACC | 89910 |
rs190437547 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109494263 | ATACTCTTTCTTCTT[A/C/G]TTCTTTGTACTTGCC | 89910 |
rs190508814 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109498133 | GGTGTTTGCTAGCAC[A/G]TCCTCCATAACCACG | 89910 |
rs190520635 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | UBE3B | GRCh38.p7 | 12:109540294 | TTCACTACAACCTCC[G/T]CCTCCGAGGCTCAAG | 89910 |
rs190655558 | snp | C/T | 0.000798403 | 0.0199641 | downstream-variant-500B | UBE3B | GRCh38.p7 | 12:109543965 | AGACGATGGGCCACC[C/T]GAGATGTTAGCAGCA | 89910 |
rs190711166 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | UBE3B | GRCh38.p7 | 12:109498698 | GGCTTATATCAGAGC[A/C]GCGCCTGCTTTACCT | 89910 |
rs190721391 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | UBE3B | GRCh38.p7 | 12:109523154 | TTACGGTCCTCTGAC[A/T]GGTGTCATCAAGTCC | 89910 |
rs190724371 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109482892 | TGGAATAAGCTATAC[A/G]TAAAACCAAATATCT | 89910 |
rs190742542 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109522194 | GAGGAGGGCCTTCTA[C/T]GGTGCCCAGCCAGCT | 89910 |
rs190753239 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109482153 | ACCTCTAGGAGATAA[C/T]ACTATTAAGTCCAAT | 89910 |
rs190803926 | snp | C/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109527453 | AGTGACAAGTGAGGG[C/G]TCAGTCCCACCTGGT | 89910 |
rs190854127 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109486781 | TAAACTGCTTGCCAC[A/G]CCACAGCCTCCATGG | 89910 |
rs190858458 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109486178 | CACACACAAATGCAA[A/G]TAAGTAGTGGATGGA | 89910 |
rs190869941 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109527602 | CGTCAGGAGAACAGA[A/C]CCTGTTTTCATAATG | 89910 |
rs190888569 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109506523 | CCGGCTGATTTTGTA[C/T]TTTTTAGTAGAGACA | 89910 |
rs190906964 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3B | GRCh38.p7 | 12:109524245 | GGCCCCTCACATCCC[C/T]CTGTGGGCAGTCCCA | 89910 |