SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3675409 | snp | A/G | 0.290657 | 0.246672 | intron-variant | Ubxn2b | GRCm38.p3 | 4:6215262 | TTCTGTATAGCAACA[A/G]CATAATGGAAATGCA | 68053 |
rs3720410 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Ubxn2b | Mm_Celera | 4:6211389 | GGGGAATGCCAGGAT[A/G]GGGAGGCAGTGGGTG | 68053 |
rs6232756 | snp | A/C | 0.48 | 0.0979796 | upstream-variant-2KB | Ubxn2b | Mm_Celera | 4:6189156 | GCCAGCAAGATTTTG[A/C]TGAAAGGACCCTGAT | 68053 |
rs6349397 | snp | C/T | 0.21875 | 0.248039 | intron-variant | Ubxn2b | Mm_Celera | 4:6214183 | ATGCCTAGTGCTCAT[C/T]GCAGGAGCTGTATAA | 68053 |
rs6350472 | snp | A/G | 0.5 | 0 | intron-variant | Ubxn2b | Mm_Celera | 4:6214420 | TCTTCTAAGAGGTCT[A/G]GGANTAGTAAGTGGG | 68053 |
rs6350477 | snp | C/T | 0.5 | 0 | intron-variant | Ubxn2b | Mm_Celera | 4:6214424 | CTAAGAGGTCTNGGA[C/T]TAGTAAGTGGGAATC | 68053 |
rs6350879 | snp | C/T | 0.32 | 0.24 | intron-variant | Ubxn2b | Mm_Celera | 4:6214456 | TAAGCTCCAGACTAA[C/T]TTTAATATAATTAAA | 68053 |
rs6408255 | snp | G/T | 0.207612 | 0.24638 | intron-variant | Ubxn2b | Mm_Celera | 4:6211589 | TCATTTTCCAAGAGA[G/T]CCAGTCAGCCACTTA | 68053 |
rs27694093 | snp | G/T | 0.495868 | 0.0452663 | downstream-variant-500B | Ubxn2b | Mm_Celera | 4:6220274 | AGAAGTCCTGGTGCA[G/T]ATATAAGAGTGTGTG | 68053 |
rs27694094 | snp | A/G | 0.132653 | 0.220748 | downstream-variant-500B | Ubxn2b | Mm_Celera | 4:6220166 | TAAGATTTTGTATCC[A/G]TGTTGATAATGCATA | 68053 |
rs27694095 | snp | C/T | 0.426035 | 0.177515 | downstream-variant-500B | Ubxn2b | GRCm38.p3 | 4:6220088 | TTTTGGCTGTTTGCC[C/T]CTGTGTAGTTCTGAA | 68053 |
rs27694096 | snp | A/T | 0.132653 | 0.220748 | utr-variant-3-prime | Ubxn2b | Mm_Celera | 4:6219784 | ATACTCTAGGCACCA[A/T]AACTTTTAAAATGTA | 68053 |
rs27694097 | snp | A/G | 0.46875 | 0.121031 | utr-variant-3-prime | Ubxn2b | GRCm38.p3 | 4:6219620 | ATGGAATGCCTACAG[A/G]TGCATATACAAAAAG | 68053 |
rs27694098 | snp | A/G | 0.486111 | 0.0821678 | utr-variant-3-prime | Ubxn2b | GRCm38.p3 | 4:6219070 | TAAGGAAAGACCACT[A/G]GAGACCAGCCTAGGC | 68053 |
rs27694099 | snp | A/G | 0.290657 | 0.246672 | utr-variant-3-prime | Ubxn2b | Mm_Celera | 4:6218858 | GAGAGCTAAGATTTT[A/G]AATACTTGAGTCTGT | 68053 |
rs27694100 | snp | G/T | 0.132653 | 0.220748 | utr-variant-3-prime | Ubxn2b | Mm_Celera | 4:6218628 | GCAGCAGGCTCCACT[G/T]CTTCCTGGTTAGCTG | 68053 |
rs27694101 | snp | G/T | 0.132653 | 0.220748 | utr-variant-3-prime | Ubxn2b | Mm_Celera | 4:6218598 | TAGCCACATCTACCT[G/T]CTGGGATTGTCCCAG | 68053 |
rs27694102 | snp | A/G | 0.142012 | 0.225474 | utr-variant-3-prime | Ubxn2b | Mm_Celera | 4:6218565 | GCACACTGTGGCTGT[A/G]TGGAATGTCTGAGTC | 68053 |
rs27694103 | snp | A/G/T | 0.142012 | 0.225474 | utr-variant-3-prime | Ubxn2b | GRCm38.p3 | 4:6218372 | GTTGTTTACATACAC[A/G/T]AAGTATTCTACCAAG | 68053 |
rs27694104 | snp | C/T | 0.132653 | 0.220748 | utr-variant-3-prime | Ubxn2b | Mm_Celera | 4:6218307 | ACCTCCTCATTTCTT[C/T]CTATACATCAGGTTG | 68053 |
rs27694105 | snp | A/G | 0.132653 | 0.220748 | utr-variant-3-prime | Ubxn2b | Mm_Celera | 4:6217841 | GTCTGTCAAGAAACC[A/G]CAGGATCTCCTGTGA | 68053 |
rs27694106 | snp | C/T | 0.46875 | 0.121031 | utr-variant-3-prime | Ubxn2b | GRCm38.p3 | 4:6217746 | TGGCTGTCCCTGTCA[C/T]CTTCCTTTCACAGAA | 68053 |
rs27694107 | snp | A/G | 0.142012 | 0.225474 | utr-variant-3-prime | Ubxn2b | Mm_Celera | 4:6217643 | AGCGGAGTCACTGGT[A/G]TCAAGAACACAGAAT | 68053 |
rs27694108 | snp | C/T | 0.124444 | 0.216185 | utr-variant-3-prime | Ubxn2b | Mm_Celera | 4:6217405 | CATTGATTCCAGCTC[C/T]AAAACCTTACCTGGA | 68053 |
rs27694109 | snp | A/C | 0.132653 | 0.220748 | utr-variant-3-prime | Ubxn2b | Mm_Celera | 4:6217354 | TGCCAAATAAACTCA[A/C]CCCACTCACAGGTGC | 68053 |
rs27694110 | snp | A/G | 0.132653 | 0.220748 | utr-variant-3-prime | Ubxn2b | Mm_Celera | 4:6217302 | GAGGGACTGACATGC[A/G]TTTTTACCCGAGTCC | 68053 |
rs27694111 | snp | A/G | 0.277778 | 0.248452 | utr-variant-3-prime | Ubxn2b | Mm_Celera | 4:6217257 | CTTTATAGTAACCTT[A/G]GTCATTCTTCAGAGT | 68053 |
rs27694112 | snp | C/T | 0.132653 | 0.220748 | utr-variant-3-prime | Ubxn2b | Mm_Celera | 4:6217176 | CAACAGCCAGCATTG[C/T]GGCTCTGTGACAATG | 68053 |
rs27694113 | snp | C/G | 0.132653 | 0.220748 | utr-variant-3-prime | Ubxn2b | Mm_Celera | 4:6217021 | AGCACCGGTTTAGAA[C/G]TATGTAAGTGGAAAG | 68053 |
rs27694114 | snp | C/T | 0.49827 | 0.0293608 | utr-variant-3-prime | Ubxn2b | GRCm38.p3 | 4:6216930 | TTTGCCCCCTGAGCT[C/T]CTCCTATCCGTGGTC | 68053 |
rs27694115 | snp | C/T | 0.49827 | 0.0293608 | utr-variant-3-prime | Ubxn2b | Mm_Celera | 4:6216714 | TGTCTGGATCACAGT[C/T]GTTCACTCATTCAGC | 68053 |
rs27694116 | snp | A/G | 0.142012 | 0.225474 | utr-variant-3-prime | Ubxn2b | Mm_Celera | 4:6216642 | AAGTCATCAGCTCTT[A/G]GTAAGATGTGATAAA | 68053 |
rs27694117 | snp | A/G | 0.142012 | 0.225474 | utr-variant-3-prime | Ubxn2b | Mm_Celera | 4:6216488 | TCCCCTGATTTTGAA[A/G]TTGTTTGTTCATACA | 68053 |
rs27694118 | snp | A/G | 0.132653 | 0.220748 | utr-variant-3-prime | Ubxn2b | Mm_Celera | 4:6216415 | CACTCAAGTTTCTTA[A/G]TGTAGCAGTGACCAG | 68053 |
rs27694119 | snp | A/G | 0.132653 | 0.220748 | utr-variant-3-prime | Ubxn2b | Mm_Celera | 4:6216327 | CTTATTACATGCTCA[A/G]TGCTAAATGTAATAA | 68053 |
rs27694120 | snp | A/G | 0.456747 | 0.140554 | utr-variant-3-prime | Ubxn2b | GRCm38.p3 | 4:6216307 | TAAATGTTTAGATCA[A/G]TCAACTTATTACATG | 68053 |
rs27694121 | snp | A/C | 0.132653 | 0.220748 | utr-variant-3-prime | Ubxn2b | Mm_Celera | 4:6216086 | ATAGTATTGCTCCAA[A/C]CCGTGTAGTGGCATA | 68053 |
rs27694122 | snp | C/G | 0.132653 | 0.220748 | missense | Ubxn2b | Mm_Celera | 4:6216016 | AACTAACAGATGAAA[C/G]CGTGACACTACAAGA | 68053 |
rs27694123 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Ubxn2b | Mm_Celera | 4:6215649 | CCGGGGTCCACAGAT[C/G]ACTTAGACACTTAGG | 68053 |
rs27694124 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Ubxn2b | Mm_Celera | 4:6215426 | TTAGTTAAGTCACTA[A/G]GTATATGTGAGAGTG | 68053 |
rs27694125 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Ubxn2b | Mm_Celera | 4:6215326 | CTCTAATACACTGCT[C/T]CATTGTCTCTTTGAT | 68053 |
rs27694126 | snp | G/T | 0.142012 | 0.225474 | intron-variant | Ubxn2b | Mm_Celera | 4:6215275 | CAACATAATGGAAAT[G/T]CATGGCATAAGCAGT | 68053 |
rs27694127 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Ubxn2b | Mm_Celera | 4:6215060 | AAACTGAGCCAAATG[A/G]ACTCAGATTTAAGCT | 68053 |
rs27694128 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Ubxn2b | Mm_Celera | 4:6214806 | GCACACACCGGTAAG[C/T]GGCTCTGCCAGCTGG | 68053 |
rs27694129 | snp | A/G | 0.132653 | 0.220748 | missense | Ubxn2b | Mm_Celera | 4:6214703 | AAATCAATACTGAAT[A/G]CAGCTGTTCTTATTG | 68053 |
rs27694130 | snp | C/T | 0.21875 | 0.248039 | intron-variant | Ubxn2b | Mm_Celera | 4:6214541 | TCCTCTGAGGGATCC[C/T]AGCACAGTTGACTGG | 68053 |
rs27694131 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Ubxn2b | Mm_Celera | 4:6213779 | GCTAATCTGAACAGC[A/G]GTTGTCTCTCACCAG | 68053 |
rs27694132 | snp | A/G | 0.21875 | 0.248039 | intron-variant | Ubxn2b | Mm_Celera | 4:6213668 | AAACAGCATTATGAA[A/G]TAGCTTTATATCATA | 68053 |
rs27694133 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Ubxn2b | Mm_Celera | 4:6213425 | GTACTTCATTTTTGT[C/T]TCAGAAAAAGCTTAG | 68053 |
rs27694134 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Ubxn2b | Mm_Celera | 4:6213205 | CACTGAATTTAGCCA[C/T]ATAACCTCAATGCCT | 68053 |
rs27694135 | snp | G/T | 0.32 | 0.24 | intron-variant | Ubxn2b | GRCm38.p3 | 4:6213168 | GCCTTCAACAGCAAA[G/T]AAAAGTGGCTCTGAA | 68053 |
rs27694136 | snp | A/C | 0.304688 | 0.243945 | intron-variant | Ubxn2b | Mm_Celera | 4:6213145 | CAGGATGAGTCACGG[A/C]CTCGAAAGCCTTCAA | 68053 |
rs27694137 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Ubxn2b | Mm_Celera | 4:6213072 | TTGCTGTCCACGGGT[A/G]TCATCCCTGTAGTAA | 68053 |
rs27694138 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Ubxn2b | Mm_Celera | 4:6213039 | CACTGTAGTGTGGTG[A/G]TTGAATAAGGGGGAA | 68053 |
rs27694139 | snp | C/G | 0.142012 | 0.225474 | intron-variant | Ubxn2b | Mm_Celera | 4:6212175 | GTTCTAGTCCCACAT[C/G]ACATGCTTAAGCACA | 68053 |
rs27694140 | snp | A/T | 0.152778 | 0.230321 | intron-variant | Ubxn2b | Mm_Celera | 4:6208662 | ACACTCAGACAAATA[A/T]GTTCTCAAAGTTAGA | 68053 |
rs27694141 | snp | C/G/T | 0.152778 | 0.230321 | intron-variant | Ubxn2b | Mm_Celera | 4:6208522 | ACATGTGTGTATGCA[C/G/T]ATGCCATCATGAGAT | 68053 |
rs27694142 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Ubxn2b | Mm_Celera | 4:6208319 | AGAGATTATTAAAGT[C/T]GGAAAAAGAGAGCTT | 68053 |
rs27694143 | snp | A/C | 0.165289 | 0.235211 | intron-variant | Ubxn2b | Mm_Celera | 4:6207830 | TAGAGTTAGAAATAG[A/C]TATTTGCAGCCAGGT | 68053 |
rs27694144 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Ubxn2b | GRCm38.p3 | 4:6207739 | CAGCCTCTGCCCTGG[A/G]CACTGAAGAATCGTG | 68053 |
rs27694145 | snp | A/G | 0.18 | 0.24 | intron-variant | Ubxn2b | Mm_Celera | 4:6207708 | TAAGACCAGTCTTCC[A/G]TAGCCCTGGGTTCCA | 68053 |
rs27694146 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Ubxn2b | Mm_Celera | 4:6207595 | TATTTGTATGACGGA[A/T]TAGACTTAGGCTCCG | 68053 |
rs27694147 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Ubxn2b | Mm_Celera | 4:6207474 | CTTAATTACTGTTAG[C/T]GGTACTCATTCTAGG | 68053 |
rs27694148 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Ubxn2b | Mm_Celera | 4:6207024 | TACATGAAAACCAAC[A/G]TTGTTCAAACTCACG | 68053 |
rs27694149 | snp | A/T | 0.152778 | 0.230321 | intron-variant | Ubxn2b | Mm_Celera | 4:6206933 | AAGTCATTGGTGGCA[A/T]GTACTTGGATATAGC | 68053 |
rs27694150 | snp | C/T | 0.165289 | 0.235211 | intron-variant | Ubxn2b | Mm_Celera | 4:6206902 | AAAGGCACAAAATGC[C/T]ATCAATGGAGTGCTG | 68053 |
rs27694151 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ubxn2b | GRCm38.p3 | 4:6205060 | TCTATGACATATTAC[C/T]TAAGTGACTTGGGGG | 68053 |
rs27694152 | snp | A/G | 0.396694 | 0.202437 | missense | Ubxn2b | GRCm38.p3 | 4:6204631 | AATTGAGGCCTTACA[A/G]TGACCCAACAAATGC | 68053 |
rs27694153 | snp | G/T | 0.32 | 0.24 | intron-variant | Ubxn2b | Mm_Celera | 4:6204028 | ACATTTAGAGATGTA[G/T]AACTGTTTGTGGAAG | 68053 |
rs27694154 | snp | A/G | 0.18 | 0.24 | intron-variant | Ubxn2b | Mm_Celera | 4:6204006 | GTGTTTCTATCTGCT[A/G]TGTCTTACATTTAGA | 68053 |
rs27694155 | snp | A/G | 0.277778 | 0.248452 | synonymous-codon | Ubxn2b | Mm_Celera | 4:6203827 | CTTCTACAAGCGATC[A/G]GAGTATATCTATGGG | 68053 |
rs27694156 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Ubxn2b | Mm_Celera | 4:6203702 | TTTAGTCTATCAAGT[A/G]TAAGAATAACATTTT | 68053 |
rs27694157 | snp | G/T | 0.152778 | 0.230321 | intron-variant | Ubxn2b | Mm_Celera | 4:6203650 | TTCATCCCAATATAT[G/T]TTCCTAGTCAATTTG | 68053 |
rs27694158 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Ubxn2b | GRCm38.p3 | 4:6202772 | AGCCAATTTGCTATA[A/G]GATTAAATTGTGACT | 68053 |
rs27694159 | snp | G/T | 0.165289 | 0.235211 | intron-variant | Ubxn2b | Mm_Celera | 4:6201948 | AGAAGAAAGCTTCGT[G/T]TGTAATCATATGTGG | 68053 |
rs27694160 | snp | A/G | 0.497041 | 0.0383476 | intron-variant | Ubxn2b | GRCm38.p3 | 4:6201392 | CACTTGTCAGTTTAG[A/G]AGAAAACCTTGAAGA | 68053 |
rs27694161 | snp | C/T | 0.165289 | 0.235211 | intron-variant | Ubxn2b | Mm_Celera | 4:6201379 | AATTTCCCTGTGTCA[C/T]TTGTCAGTTTAGGAG | 68053 |
rs27694162 | snp | A/G | 0.493827 | 0.0552116 | intron-variant | Ubxn2b | GRCm38.p3 | 4:6201242 | GGAAAGCCTGGTGGG[A/G]TCTAGTGTAGTCAGT | 68053 |
rs27694163 | snp | G/T | 0.152778 | 0.230321 | intron-variant | Ubxn2b | GRCm38.p3 | 4:6200902 | AAGACACTGCTTGAA[G/T]AAAATACAGTGCTTG | 68053 |
rs27694164 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Ubxn2b | Mm_Celera | 4:6200847 | CCCTTATGCTATATG[C/T]AGCCATCAAATTGTG | 68053 |
rs27694165 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Ubxn2b | Mm_Celera | 4:6200819 | CAAAAGGAAGAAATT[A/G]GTGTTGTCCTCTCCC | 68053 |
rs27694166 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Ubxn2b | Mm_Celera | 4:6200701 | GAGACTGACCAGTAA[A/G]CCAAGATCCAAATTC | 68053 |
rs27694167 | snp | G/T | 0.142012 | 0.225474 | intron-variant | Ubxn2b | Mm_Celera | 4:6200631 | CATGAAGAACCCAAG[G/T]TCAGGATTTAAAGTA | 68053 |
rs27694168 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Ubxn2b | Mm_Celera | 4:6200562 | TGGAACATGTTTATT[A/G]CACCAGTTGTAAATA | 68053 |
rs27694169 | snp | G/T | 0.197531 | 0.244432 | intron-variant | Ubxn2b | Mm_Celera | 4:6200369 | GAGAGGATAAATATT[G/T]TGTTGATCAAATAAG | 68053 |
rs27694170 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Ubxn2b | Mm_Celera | 4:6200240 | AGTCAAACAAAGTAA[A/G]GAAGTGCTAAGCATG | 68053 |
rs27694171 | snp | A/T | 0.142012 | 0.225474 | intron-variant | Ubxn2b | Mm_Celera | 4:6199396 | CTTTGAGTGATAAAG[A/T]GCTGTCATGACAAGA | 68053 |
rs27694172 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Ubxn2b | Mm_Celera | 4:6198926 | GTCTTCATTGTACTT[C/G]AAACGGGTGTCTTTA | 68053 |
rs27694173 | snp | A/C | 0.142012 | 0.225474 | intron-variant | Ubxn2b | Mm_Celera | 4:6198695 | CCTCTGCAACCAGTG[A/C]TGTAGTTATTAAAGA | 68053 |
rs27694174 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Ubxn2b | Mm_Celera | 4:6198296 | ACTTTTGGCTCCCTG[G/T]TTTGAGCACATGCAG | 68053 |
rs27694175 | snp | A/G | 0.21875 | 0.248039 | intron-variant | Ubxn2b | Mm_Celera | 4:6198189 | TGAGTATATGTAGAT[A/G]TGTGTAATATGTTAA | 68053 |
rs27694176 | snp | A/C | 0.277778 | 0.248452 | intron-variant | Ubxn2b | Mm_Celera | 4:6198141 | TGGTTTGAATATACT[A/C]TCCTTTGATGTAATT | 68053 |
rs27694177 | snp | A/C | 0.142012 | 0.225474 | intron-variant | Ubxn2b | Mm_Celera | 4:6197805 | TTAATGCAGGGCATC[A/C]TCTCTTTTTTGTCTG | 68053 |
rs27694178 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Ubxn2b | Mm_Celera | 4:6197757 | ACCCAGTTAGAGACT[A/G]CTCATTGCATCTGAT | 68053 |
rs27694179 | snp | C/T | 0.429688 | 0.173817 | intron-variant | Ubxn2b | Mm_Celera | 4:6197587 | TTATAGCCACTGTGA[C/T]GCTCAACTCTAGATA | 68053 |
rs31757966 | snp | A/G | 0.32 | 0.24 | upstream-variant-2KB | Ubxn2b | Mm_Celera | 4:6190969 | AGTGCGCACCGGCTG[A/G]TGGGGGGAAAAGGAG | 68053 |
rs31788419 | snp | C/T | 0.444444 | 0.157135 | upstream-variant-2KB | Ubxn2b | Mm_Celera | 4:6189735 | TGACCACCTCATAAT[C/T]GCTTCTAAAAAAAAA | 68053 |
rs31792390 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ubxn2b | Mm_Celera | 4:6195912 | CATAAATGACTAAAA[C/T]CTATATTTACTTCAT | 68053 |
rs31878506 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ubxn2b | Mm_Celera | 4:6204048 | GTTTGTGGAAGGAAT[A/G]TAATTCTTATAATTT | 68053 |
rs31920293 | snp | C/G | 0.375 | 0.216506 | intron-variant | Ubxn2b | GRCm38.p3 | 4:6211213 | AATCAACCAGACCCT[C/G]CCCCCCCCCCCAAGA | 68053 |