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 |