SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs7958 | snp | A/G | 0.452965 | 0.145963 | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58451294 | GATGAACAGTATTTC[A/G]TGTGTGCTATGTAGT | 137886 |
rs11752 | snp | A/G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58451079 | TTAAAAGAATTGAAC[A/G/T]TTGTAAATCAAAGGG | 137886 |
rs726012 | snp | A/G | 0.281313 | 0.248031 | intron-variant | UBXN2B | GRCh38.p7 | 8:58429796 | ACATGGAGACTTCCA[A/G]GGTAAGATGACAATC | 137886 |
rs1001706 | snp | C/T | 0.274661 | 0.248781 | intron-variant | UBXN2B | GRCh38.p7 | 8:58427355 | gtagtcccaactgct[C/T]gggaggctgaggtgg | 137886 |
rs1052499 | snp | A/T | | | intron-variant, utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58434927 | TTAATGTGGCATTAC[A/T]GCTGGCAGAAGATTT | 137886 |
rs1057067 | snp | C/T | 0.386884 | 0.209196 | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58450065 | gtgtgtgacctgata[C/T]tcagaccttttgatg | 137886 |
rs1060966 | snp | A/G | 0 | 0 | intron-variant | UBXN2B | GRCh38.p7 | 8:58443531 | ggcacagtggctcac[A/G]cctgtaatcccagca | 137886 |
rs1469338 | snp | A/G | 0.264906 | 0.249555 | intron-variant | UBXN2B | GRCh38.p7 | 8:58444897 | ACTTCCATTCAAAAA[A/G]CTTCTCTCTCAGAGT | 137886 |
rs1471104 | snp | A/G | 0 | 0 | intron-variant | UBXN2B | GRCh38.p7 | 8:58444610 | AAATCCAAGAGAAAA[A/G]ACATGAGACACTGAA | 137886 |
rs1529367 | snp | G/T | 0.398354 | 0.201224 | intron-variant | UBXN2B | GRCh38.p7 | 8:58427544 | TACAATGAACACCTT[G/T]AAAATATCCTGCATT | 137886 |
rs1529368 | snp | C/T | 0.366266 | 0.221319 | intron-variant | UBXN2B | GRCh38.p7 | 8:58427366 | AAGCTATCCTGCCAC[C/T]TCAGCCTCCCGAGCA | 137886 |
rs1988172 | snp | A/G | 0.127944 | 0.218179 | intron-variant | UBXN2B | GRCh38.p7 | 8:58422687 | TTTCCCAAGTCTGGG[A/G]GTGCCCCAGTGGGGT | 137886 |
rs1993453 | snp | A/G | 0.39979 | 0.200158 | intron-variant | UBXN2B | GRCh38.p7 | 8:58434625 | GAATATATTAAATAA[A/G]TGGTTGCTGGGGGTG | 137886 |
rs2016886 | snp | C/T | 0.365853 | 0.221536 | intron-variant | UBXN2B | GRCh38.p7 | 8:58415171 | TGTCATTGGGGGTAT[C/T]ACGTGCTATGAGTAT | 137886 |
rs2033142 | snp | C/T | 0 | 0 | intron-variant | UBXN2B | GRCh38.p7 | 8:58424668 | TGTACTCCAACTCCA[C/T]GCTGTGCAGAAATGA | 137886 |
rs2081688 | snp | A/C | 0.387074 | 0.209071 | intron-variant | UBXN2B | GRCh38.p7 | 8:58438595 | GTAAACATTCCCATT[A/C]CAAAAGAGAGATCTG | 137886 |
rs2081689 | snp | C/T | 0.453697 | 0.14494 | intron-variant | UBXN2B | GRCh38.p7 | 8:58438468 | CATATACAGGGCATA[C/T]TGGTGCAAGAGGTGG | 137886 |
rs2162460 | snp | G/T | 0.127944 | 0.218179 | intron-variant | UBXN2B | GRCh38.p7 | 8:58419222 | TAGAAGATATCATAC[G/T]TAGAAAAAAAGATTG | 137886 |
rs2288313 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | UBXN2B | GRCh38.p7 | 8:58434601 | TATATTCCAGGAACT[A/G]CTTCTTGAAAACCCG | 137886 |
rs2326075 | snp | C/T | 0.38286 | 0.211774 | intron-variant | UBXN2B | GRCh38.p7 | 8:58413167 | TTCCACCCTAAGTTA[C/T]GATGGGGATTTTTTT | 137886 |
rs2326076 | snp | G/T | 0 | 0 | intron-variant | UBXN2B | GRCh38.p7 | 8:58446259 | TGAAATATGTGGTAT[G/T]TAAACAGTCTCTATA | 137886 |
rs2859998 | snp | A/G | 0.451359 | 0.148171 | intron-variant | UBXN2B | GRCh38.p7 | 8:58411603 | GGGATAGAATCCGGC[A/G]CCCGGTCTCCCGATG | 137886 |
rs3080297 | in-del | -/AT/T/TT | 0.58495 | 0.107276 | intron-variant | UBXN2B | GRCh38.p7 | 8:58434369 | tatatatatatatat[-/AT/T/TT]tTTTTTTTTTTCTAT | 137886 |
rs3857966 | snp | A/G | | | upstream-variant-2KB | UBXN2B | GRCh38.p7 | 8:58410760 | TATATATGTGTGTGT[A/G]TATATATATATATAT | 137886 |
rs4599797 | snp | A/C | 0.271702 | 0.249056 | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58449319 | CCCACCCCCCGCTCC[A/C]CTCCTGTGTTAAAGA | 137886 |
rs5891685 | in-del | -/TTTA | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58446258 | ATGAAATATGTGGTA[-/TTTA]AACAGTCTCTATAAA | 137886 |
rs6982486 | snp | A/G | 0.399073 | 0.200692 | intron-variant | UBXN2B | GRCh38.p7 | 8:58420135 | GCTTTGACTCAAGAT[A/G]GATACATCTCAGTTG | 137886 |
rs6993992 | snp | C/T | 0.453697 | 0.14494 | intron-variant | UBXN2B | GRCh38.p7 | 8:58436494 | cccctacctcgacac[C/T]gaatgacagcagTGC | 137886 |
rs6997864 | snp | A/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58447301 | ATATAAAGATTAAAA[A/T]TTTGTGATTTTTATT | 137886 |
rs7006025 | snp | A/G | 0.281577 | 0.247998 | intron-variant | UBXN2B | GRCh38.p7 | 8:58442494 | AAATGAAAATAATCT[A/G]TTGTCTTCCATAGAT | 137886 |
rs7007181 | snp | C/T | 0.363359 | 0.222822 | intron-variant | UBXN2B | GRCh38.p7 | 8:58426720 | TCCGTGACAGACCCG[C/T]TCCTTGCTCAGGCTC | 137886 |
rs7010273 | snp | C/G | 0.00953873 | 0.0683987 | intron-variant | UBXN2B | GRCh38.p7 | 8:58446137 | TATCTAAGTAGAACT[C/G]TATGTGACTTGAGTA | 137886 |
rs7012712 | snp | G/T | 0.00953873 | 0.0683987 | intron-variant | UBXN2B | GRCh38.p7 | 8:58427886 | AGGATATGGGCATAT[G/T]TATGTAAGAGGAGGA | 137886 |
rs7813734 | snp | C/T | 0.0599851 | 0.162463 | downstream-variant-500B | UBXN2B | GRCh38.p7 | 8:58451712 | CAGGTGCTTCTTTTT[C/T]GCCACAATGGATTTC | 137886 |
rs7817066 | snp | A/C | 0.0275645 | 0.114116 | intron-variant | UBXN2B | GRCh38.p7 | 8:58425958 | TCTGGCTCTCTCATA[A/C]AAGAAAACTACCATG | 137886 |
rs7822723 | snp | G/T | 0.14665 | 0.227637 | intron-variant | UBXN2B | GRCh38.p7 | 8:58427327 | AAATAGCCAAGCGTG[G/T]TGGTGCACGCCTGTA | 137886 |
rs7823397 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58442978 | ACTTCAAAGCCTTAC[C/T]TTATCTCAGCTCCTC | 137886 |
rs7823985 | snp | G/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58446865 | tgcagtggcggaatc[G/T]cagcccactacaaac | 137886 |
rs7826302 | snp | A/T | | | upstream-variant-2KB | UBXN2B | GRCh38.p7 | 8:58410790 | tatatatatatatat[A/T]tttttttttttagta | 137886 |
rs7827559 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58446920 | ctcatgctcagcctc[C/T]tgagtagctgggatt | 137886 |
rs7829017 | snp | C/T | 0.449599 | 0.150533 | intron-variant | UBXN2B | GRCh38.p7 | 8:58414276 | CCAGAGTGTGATTCA[C/T]TGGTTCTAGAGTAGA | 137886 |
rs7830535 | snp | A/G | 0.281313 | 0.248031 | intron-variant | UBXN2B | GRCh38.p7 | 8:58441184 | GTTTTGTAGAGACAC[A/G]TGTCTTACTATGTTG | 137886 |
rs7835967 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58442726 | GCTAGAGTAGTGCCT[A/G]ACAAAATCACAGAGT | 137886 |
rs7836166 | snp | A/G | 0 | 0 | intron-variant | UBXN2B | GRCh38.p7 | 8:58442596 | GCAAACCAAAATGCT[A/G]TAAAAATGTTACATA | 137886 |
rs7836229 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58442828 | AATCATGATTTGAAG[C/T]TGATGTTTCTGCAGA | 137886 |
rs7836301 | snp | A/G | 0 | 0 | intron-variant | UBXN2B | GRCh38.p7 | 8:58442692 | AAACTGTATTATTGA[A/G]TAAAAATTAGCTTGG | 137886 |
rs7839859 | snp | C/G | 0 | 0 | intron-variant | UBXN2B | GRCh38.p7 | 8:58442951 | TAGACCCTGAGGGCT[C/G]TCTTCTCTAAAACTT | 137886 |
rs7839907 | snp | A/C | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58443131 | GCTGctttcctaaac[A/C]ccctcctcgacccct | 137886 |
rs7840036 | snp | C/T | 0 | 0 | intron-variant | UBXN2B | GRCh38.p7 | 8:58446748 | CATATGCTGCTAACA[C/T]ATTTTATACTCCGAA | 137886 |
rs7840636 | snp | A/C | 0.147991 | 0.228242 | intron-variant | UBXN2B | GRCh38.p7 | 8:58443637 | ATCTCTACTAAAAAT[A/C]CAAAAAAAAAAAAAA | 137886 |
rs7843633 | snp | A/T | 0 | 0 | intron-variant | UBXN2B | GRCh38.p7 | 8:58446983 | ttctggttttagtag[A/T]gacggggttttcacc | 137886 |
rs7844732 | snp | C/G | 0.382085 | 0.212258 | intron-variant | UBXN2B | GRCh38.p7 | 8:58414041 | GGGAGGGAGTGGGAA[C/G]AGGGATAACTTCAGT | 137886 |
rs10095270 | snp | C/T | 0.264906 | 0.249555 | intron-variant | UBXN2B | GRCh38.p7 | 8:58440339 | TTGCAGCAGGAGCAA[C/T]GTGCTTAGCTTTGTG | 137886 |
rs10108817 | snp | C/T | 0.269267 | 0.249256 | intron-variant | UBXN2B | GRCh38.p7 | 8:58431590 | ataaatgctcagaag[C/T]gcaattggtagatca | 137886 |
rs10110824 | snp | C/G | 0.271162 | 0.249103 | intron-variant | UBXN2B | GRCh38.p7 | 8:58423210 | TTGAGCTCTTGGGAG[C/G]TCTGAGCTTCATGTC | 137886 |
rs10111761 | snp | C/T | 0.26518 | 0.249539 | intron-variant | UBXN2B | GRCh38.p7 | 8:58437763 | agagcccgttgaagt[C/T]tggaaaattctcatc | 137886 |
rs10504254 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | UBXN2B | GRCh38.p7 | 8:58421589 | ATTACTGACTGGGCT[C/T]TCTCATTACTGGCCC | 137886 |
rs10957054 | snp | C/T | 0.363776 | 0.222609 | intron-variant | UBXN2B | GRCh38.p7 | 8:58423997 | TTTTCTATGACTCTT[C/T]AATGCCAATGCAAAG | 137886 |
rs11552203 | snp | A/G | 0.228842 | 0.249103 | utr-variant-3-prime, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58450546 | CCTTTCTTCAAGGCC[A/G]CCCTAGCATTAACAT | 137886 |
rs11988442 | snp | A/C | 0.281049 | 0.248064 | intron-variant | UBXN2B | GRCh38.p7 | 8:58426104 | CCATTCTTCTCTTTT[A/C]ATTGCCCGTGATGTT | 137886 |
rs11989326 | snp | C/T | 0.281049 | 0.248064 | intron-variant | UBXN2B | GRCh38.p7 | 8:58430723 | ATTTTACCTCCTCTT[C/T]CATTTTTCTATTATT | 137886 |
rs11995825 | snp | C/T | 0.287606 | 0.247155 | intron-variant | UBXN2B | GRCh38.p7 | 8:58420978 | TCCCCCAACAACATA[C/T]AGAAAATAAAAACTG | 137886 |
rs11996829 | snp | G/T | 0.398894 | 0.200825 | intron-variant | UBXN2B | GRCh38.p7 | 8:58418723 | CTTTGTAATCAGCAG[G/T]TTGGTATCTTGACAC | 137886 |
rs12543440 | snp | A/G | 0.383439 | 0.21141 | intron-variant | UBXN2B | GRCh38.p7 | 8:58420837 | AAGATACAATAAACT[A/G]TATTTTGGAACTTTT | 137886 |
rs12543860 | snp | A/G | 0.453818 | 0.144769 | intron-variant | UBXN2B | GRCh38.p7 | 8:58433386 | ACCAATGATGTGTGA[A/G]TTTTCAGTCTCGATC | 137886 |
rs12545520 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58437330 | tttcttttttttttt[C/T]ttttttttttttttt | 137886 |
rs12546328 | snp | C/T | 0.453087 | 0.145793 | intron-variant | UBXN2B | GRCh38.p7 | 8:58442117 | AGAGTTTCCACTTTG[C/T]AGTGCTTACTTCCAC | 137886 |
rs12547722 | snp | A/C | 0.387453 | 0.208822 | intron-variant | UBXN2B | GRCh38.p7 | 8:58437201 | ttgggaactggagta[A/C]aggtcagccttgtta | 137886 |
rs12676903 | snp | C/T | 0.453818 | 0.144769 | intron-variant | UBXN2B | GRCh38.p7 | 8:58445478 | AAGGACTTACTGGTA[C/T]AATATACCTTCATAA | 137886 |
rs12681594 | snp | C/T | 0.383439 | 0.21141 | intron-variant | UBXN2B | GRCh38.p7 | 8:58418657 | TAGTGATATGTTCAT[C/T]TGGTTAAGGTGCTGA | 137886 |
rs13252159 | snp | C/G | 0.287346 | 0.247195 | intron-variant | UBXN2B | GRCh38.p7 | 8:58424692 | GAGTACAAGGCGGGG[C/G]GGGGGGCTCTGATCT | 137886 |
rs13253288 | snp | C/G | 0.399253 | 0.200558 | intron-variant | UBXN2B | GRCh38.p7 | 8:58426297 | CTGTAAGCTCCGCCT[C/G]CTGGGTTCATGCCAT | 137886 |
rs13253349 | snp | A/G | 0.451109 | 0.148509 | intron-variant | UBXN2B | GRCh38.p7 | 8:58411926 | GGTTCCATTTTATCA[A/G]GTAGGTTTTTCTTTT | 137886 |
rs13260971 | snp | C/T | 0.234109 | 0.249494 | upstream-variant-2KB | UBXN2B | GRCh38.p7 | 8:58409883 | ctttatacatcaaaa[C/T]gatcagtatgccaaa | 137886 |
rs13263105 | snp | C/G | 0.399611 | 0.200291 | intron-variant | UBXN2B | GRCh38.p7 | 8:58413036 | AGTGAGAACAGCTTG[C/G]TTAATGACCACCTGA | 137886 |
rs13265462 | snp | A/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58446780 | AAAGTACAACCTGCA[A/T]TTTTTtttttttttt | 137886 |
rs13271316 | snp | C/G | 0.278664 | 0.248351 | intron-variant | UBXN2B | GRCh38.p7 | 8:58419430 | TTTCATTATCTGAAA[C/G]TCTGGACATAAGATG | 137886 |
rs13277110 | snp | A/G | 0.271702 | 0.249056 | intron-variant | UBXN2B | GRCh38.p7 | 8:58423687 | tgatccgccagcctc[A/G]gcctcccaaagtgct | 137886 |
rs13277646 | snp | A/G | 0.414862 | 0.187938 | synonymous-codon, nc-transcript-variant | UBXN2B | GRCh38.p7 | 8:58416879 | ATTGTATGAAGATGA[A/G]GTGAAGTGCAAATCT | 137886 |
rs13277801 | snp | C/T | 0.39979 | 0.200158 | intron-variant | UBXN2B | GRCh38.p7 | 8:58440975 | TCGTCTCTCTTTACA[C/T]GTCAGGCTTCTCTTT | 137886 |
rs13278695 | snp | C/T | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58441261 | ggcctgccaaagtgc[C/T]tgggttacaggcatg | 137886 |
rs13279410 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58441369 | TATATATATATATAT[A/G]TATGTGTATATATAT | 137886 |
rs13279416 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58441375 | tatatatatgtatgt[A/G]tatatatatgtatgt | 137886 |
rs13279425 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58441385 | tatgtgtatatatat[A/G]tatgtatgtgtatat | 137886 |
rs13279635 | snp | A/G | | | intron-variant | UBXN2B | GRCh38.p7 | 8:58441395 | tatatgtatgtatgt[A/G]tatatatagtatgta | 137886 |
rs13281822 | snp | A/G | 0.383439 | 0.21141 | intron-variant | UBXN2B | GRCh38.p7 | 8:58420748 | GTTATATGACCCACT[A/G]AAACCAACTGTTCAA | 137886 |
rs16923442 | snp | A/G | 0.14665 | 0.227637 | intron-variant | UBXN2B | GRCh38.p7 | 8:58411844 | GTCACCTGAACAGTA[A/G]TGATACGTGATTTGT | 137886 |
rs16923447 | snp | A/G | 0.290706 | 0.248569 | intron-variant | UBXN2B | GRCh38.p7 | 8:58417607 | TTCTTGTTGCCAGGA[A/G]TATTTTCATTAACAT | 137886 |
rs16923452 | snp | A/G | 0.448066 | 0.152544 | intron-variant | UBXN2B | GRCh38.p7 | 8:58419034 | ATGCTGTCTGAAACA[A/G]TGCTGTGATTAATAG | 137886 |
rs16923455 | snp | C/G | 0.14665 | 0.227637 | intron-variant | UBXN2B | GRCh38.p7 | 8:58426615 | AAACTGCTGTCAGCT[C/G]CTCTTATCAACAGTG | 137886 |
rs16923457 | snp | A/T | 0.153997 | 0.230832 | intron-variant | UBXN2B | GRCh38.p7 | 8:58429314 | GTCGTCGCTCCCTAA[A/T]ATAATCTGCTTCTAA | 137886 |
rs16923459 | snp | C/G | 0.0209421 | 0.100162 | intron-variant | UBXN2B | GRCh38.p7 | 8:58429772 | TAAGTATTTTAACAA[C/G]TGAAGTTTGATTGTC | 137886 |
rs16923468 | snp | A/C | 0.0197882 | 0.097481 | intron-variant | UBXN2B | GRCh38.p7 | 8:58430002 | TAACAAACGCAGGGG[A/C]TTTTAAGGGAGTAGG | 137886 |
rs16923469 | snp | A/C | 0.0471551 | 0.14613 | intron-variant | UBXN2B | GRCh38.p7 | 8:58430135 | ACTAGGTCTCTACTG[A/C]GTGTGGCCTTCTTAG | 137886 |
rs16923472 | snp | C/G | 0.293482 | 0.24619 | intron-variant | UBXN2B | GRCh38.p7 | 8:58433146 | AATTTTAACTCACTT[C/G]CTATGTATTTTAGTC | 137886 |
rs16923480 | snp | C/T | 0.281841 | 0.247964 | intron-variant | UBXN2B | GRCh38.p7 | 8:58440610 | AAGTTACCCTCTACT[C/T]GTCCACATATTGTTG | 137886 |
rs17261333 | snp | A/G | 0.114036 | 0.209795 | intron-variant | UBXN2B | GRCh38.p7 | 8:58426627 | GCTCCTCTTATCAAC[A/G]GTGGGTTTTCTGCCT | 137886 |
rs17261550 | snp | G/T | 0.272241 | 0.249009 | intron-variant | UBXN2B | GRCh38.p7 | 8:58430226 | ATTAGTGAATGAGAT[G/T]TATGTGATAAGCAGT | 137886 |
rs17261584 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | UBXN2B | GRCh38.p7 | 8:58433042 | TGGTTCTTGAAGGCT[C/T]CCCAGTATGAGCCAC | 137886 |
rs28710905 | snp | C/T | 0.0452528 | 0.143452 | intron-variant | UBXN2B | GRCh38.p7 | 8:58411864 | ACGTGATTTGTTCTT[C/T]TTTGTCTTGGATGCT | 137886 |