SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs7541 | snp | C/T | 0.211664 | 0.247043 | synonymous-codon, upstream-variant-2KB | LAMTOR2, UBQLN4 | GRCh38.p7 | 1:156055305 | GGCCTACTCTGGTTA[C/T]GGGGACACTGACGCC | 56893 |
rs10919 | snp | C/G | 0.47743 | 0.103805 | utr-variant-3-prime, nc-transcript-variant | UBQLN4 | GRCh38.p7 | 1:156035640 | CTGAAAGGCCAGGGG[C/G]TCTGGAGGAAAAAAA | 56893 |
rs2095402 | snp | A/G | 0.490997 | 0.0664859 | intron-variant | UBQLN4 | GRCh38.p7 | 1:156037386 | GGATCACGAGGTCAG[A/G]AGATCGAGACCATCC | 56893 |
rs2297792 | snp | A/G | 0.487148 | 0.0791248 | missense, nc-transcript-variant | UBQLN4 | GRCh38.p7 | 1:156041653 | TGGCTCCTTTGGGAT[A/G]TCCCGGACCCCAGCA | 56893 |
rs3754293 | snp | C/T | 0.469642 | 0.119404 | upstream-variant-2KB | LAMTOR2, UBQLN4 | GRCh38.p7 | 1:156054582 | AGCGCTGGAAGGACA[C/T]TTAACCCCTTCGGGG | 56893 |
rs3820591 | snp | G/T | 0.124444 | 0.216185 | upstream-variant-2KB | LAMTOR2, UBQLN4 | GRCh38.p7 | 1:156054718 | GCCCCACCGCGGGGG[G/T]CTCTGGGAATCGTAG | 56893 |
rs3820592 | snp | A/G | 0.466412 | 0.125164 | utr-variant-3-prime, nc-transcript-variant | UBQLN4 | GRCh38.p7 | 1:156036222 | TGGAAGTTGGAATTA[A/G]CAGTGGGGAGCAGAA | 56893 |
rs7517202 | snp | C/T | 0.475259 | 0.108435 | downstream-variant-500B | UBQLN4 | GRCh38.p7 | 1:156034881 | TATATAATTTTTTTT[C/T]CTTTTGAGACAGGGT | 56893 |
rs7518081 | snp | G/T | | | intron-variant | UBQLN4 | GRCh38.p7 | 1:156038302 | gaatcacttgaatcc[G/T]ggaggcggaggtgca | 56893 |
rs7555839 | snp | A/G | 0.159622 | 0.233092 | intron-variant | UBQLN4 | GRCh38.p7 | 1:156038865 | acccaggctggatgc[A/G]gtggcatgatctgcc | 56893 |
rs10157633 | snp | C/T | 0.00424627 | 0.0458814 | intron-variant | UBQLN4 | GRCh38.p7 | 1:156048392 | AGCCAAGGCCCACCC[C/T]TCAGGGGACTGGGGA | 56893 |
rs10158536 | snp | A/G | 0.151668 | 0.229849 | intron-variant | UBQLN4 | GRCh38.p7 | 1:156047093 | TAGGAAAATAAACAA[A/G]ATACTAACAACATTA | 56893 |
rs10796957 | snp | C/T | 0.148996 | 0.228688 | intron-variant | UBQLN4 | GRCh38.p7 | 1:156052100 | CACCCTAGAAAGCCC[C/T]TGCTGCTATCTGCCT | 56893 |
rs11264430 | snp | C/T | | | intron-variant | UBQLN4 | GRCh38.p7 | 1:156039492 | TGACCTCAGGTGATC[C/T]GCCTGCCTCGGCCTC | 56893 |
rs11264431 | snp | C/T | 0.451856 | 0.147493 | upstream-variant-2KB, intron-variant | LAMTOR2, UBQLN4 | GRCh38.p7 | 1:156053011 | TGTGAAATTATGGAG[C/T]GGCCACAGGGGGTGG | 56893 |
rs11389947 | in-del | -/C | 0.0766824 | 0.180169 | intron-variant | UBQLN4 | GRCh38.p7 | 1:156050920 | ACCCTTAGCCATGGT[-/C]CCCCACCTCTGAGAA | 56893 |
rs11548484 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | UBQLN4 | GRCh38.p7 | 1:156036033 | TTATATGCACACACA[C/T]ACACATTTCCATGGA | 56893 |
rs11582305 | snp | A/T | 0.471292 | 0.116318 | | | GRCh38.p7 | 1:156033864 | AAAAAAACCAAAAAA[A/T]AAAAAACAAAAACAA | 56893 |
rs11809690 | snp | C/T | 0.00478085 | 0.0486577 | downstream-variant-500B | UBQLN4 | GRCh38.p7 | 1:156034816 | CATCATCAGTTATCC[C/T]TTAACCTTCtatata | 56893 |
rs12128541 | snp | A/G | 0.477515 | 0.103619 | | | GRCh38.p7 | 1:156034201 | CTTCCTCAAACTTAC[A/G]TGATTAGTGGTAATG | 56893 |
rs12136348 | snp | C/T | 0.482905 | 0.0908579 | intron-variant | UBQLN4 | GRCh38.p7 | 1:156046244 | tataatcccagcact[C/T]tgggaggccgaggtg | 56893 |
rs12138913 | snp | C/G | 0.137187 | 0.223099 | intron-variant | UBQLN4 | GRCh38.p7 | 1:156046196 | atattttaaaagttt[C/G]tcagttttaggccgg | 56893 |
rs12566515 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | UBQLN4 | GRCh38.p7 | 1:156036953 | CATCGAGGGAGGGGA[A/G]AGGCAGGAGGCATGG | 56893 |
rs12733778 | snp | A/G | | | intron-variant | UBQLN4 | GRCh38.p7 | 1:156047624 | ACCATggccaggcgc[A/G]gtggctcactcctgt | 56893 |
rs12735992 | snp | C/T | 0.152334 | 0.230133 | intron-variant | UBQLN4 | GRCh38.p7 | 1:156040996 | CCCTCCCCAGAGTCT[C/T]AGAGATGGGGGCTGC | 56893 |
rs12744926 | snp | G/T | | | intron-variant | UBQLN4 | GRCh38.p7 | 1:156040124 | TCTggacgggtgtgg[G/T]ggctcacgcctataa | 56893 |
rs12758906 | snp | A/T | | | intron-variant | UBQLN4 | GRCh38.p7 | 1:156047634 | ggcgcggtggctcac[A/T]cctgtaatctcagca | 56893 |
rs34005337 | snp | C/T | | | intron-variant | UBQLN4 | GRCh38.p7 | 1:156047441 | GTAGAGATGGGGTTT[C/T]ACCATTTTAGCCAGG | 56893 |
rs34008197 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | UBQLN4 | GRCh38.p7 | 1:156036169 | TCTCTTCTGCCAGCT[C/T]GGGCCTGGATTCTTC | 56893 |
rs34224286 | snp | C/T | 0.0980852 | 0.198549 | intron-variant | UBQLN4 | GRCh38.p7 | 1:156042720 | CACAAGAAACTGCCC[C/T]CAACCAAGAGGAACT | 56893 |
rs34449781 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | UBQLN4 | GRCh38.p7 | 1:156036270 | GTCTCCCCCATTCCC[C/T]TCCTCCGAATAATCT | 56893 |
rs34465438 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | UBQLN4 | GRCh38.p7 | 1:156036114 | CGCTTAGCTTCATTG[A/G]GCTCCTTTTTTCAGT | 56893 |
rs34470877 | in-del | -/C | | | intron-variant, upstream-variant-2KB | LAMTOR2, UBQLN4 | GRCh38.p7 | 1:156055671 | ATCAGTTGTGGAACC[-/C]TTGGGTAAGTCGCTT | 56893 |
rs34487584 | snp | C/T | 0 | 0 | utr-variant-3-prime, nc-transcript-variant | UBQLN4 | GRCh38.p7 | 1:156036123 | TCATTGGGCTCCTTT[C/T]TTCAGTTTAAATTCC | 56893 |
rs34542912 | snp | G/T | | | intron-variant | UBQLN4 | GRCh38.p7 | 1:156047461 | TTTTAGCCAGGATGG[G/T]CTCGATCTCCTGACC | 56893 |
rs34673835 | snp | C/T | 0.207253 | 0.246318 | intron-variant | UBQLN4 | GRCh38.p7 | 1:156043885 | CCCCCTCTGTGGCCT[C/T]GATAGTCTCACCTCT | 56893 |
rs34720108 | in-del | -/TA | | | downstream-variant-500B | UBQLN4 | GRCh38.p7 | 1:156034825 | TATCCCTTAACCTTC[-/TA]TATATATATATATAT | 56893 |
rs34790727 | in-del | -/A | | | intron-variant | UBQLN4 | GRCh38.p7 | 1:156039936 | GCGAGACTCCGTCTC[-/A]AAAAAAAAAAAAAAA | 56893 |
rs34855998 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | UBQLN4 | GRCh38.p7 | 1:156036055 | TGCATATAAGCACAT[A/G]TGCTTGAGGAACTAA | 56893 |
rs34866268 | in-del | -/T | | | intron-variant | UBQLN4 | GRCh38.p7 | 1:156039246 | CACTCCTGGCCTGGC[-/T]TTTTTTTTTTTTTTT | 56893 |
rs35030613 | in-del | -/A | | | intron-variant | UBQLN4 | GRCh38.p7 | 1:156043244 | AATATCATCTAGATC[-/A]AAACTTGTCTTAGCA | 56893 |
rs35099869 | in-del | -/G | | | intron-variant | UBQLN4 | GRCh38.p7 | 1:156048790 | TGCCCCACAGTGACA[-/G]GGGAGTAGAGTAAAC | 56893 |
rs35166144 | in-del | -/T | | | intron-variant | UBQLN4 | GRCh38.p7 | 1:156039245 | CACTCCTGGCCTGGC[-/T]TTTTTTTTTTTTTTT | 56893 |
rs35191566 | snp | C/G | | | intron-variant | UBQLN4 | GRCh38.p7 | 1:156044731 | CCCAGCCTCCTTGGA[C/G]TAATCCTAACTCCCC | 56893 |
rs35537745 | in-del | -/T | | | intron-variant | UBQLN4 | GRCh38.p7 | 1:156045079 | CTGAGGGAGTCCCAG[-/T]ACTCAGTTTTCCCTA | 56893 |
rs35603727 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | UBQLN4 | GRCh38.p7 | 1:156038197 | GCTGGCCAACATGGC[A/G]AAACCCCATGTCTAC | 56893 |
rs35632706 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant | UBQLN4 | GRCh38.p7 | 1:156035533 | TGTGCTCTGACAGAG[A/C]AATGTCCAATTCCAG | 56893 |
rs35659997 | in-del | -/T | | | intron-variant | UBQLN4 | GRCh38.p7 | 1:156047243 | TGTGTAACTTGTGAA[-/T]TTTTTTTTTTTTTTT | 56893 |
rs35772427 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | UBQLN4 | GRCh38.p7 | 1:156036390 | ACAGGGAGAACAGGC[A/G]TCTTCCTCCTTACCC | 56893 |
rs35939581 | snp | C/G/T | | | utr-variant-3-prime, nc-transcript-variant | UBQLN4 | GRCh38.p7 | 1:156036329 | TCTGGGCTGCTCCAG[C/G/T]GTTTGTTAATTCCTG | 56893 |
rs35996362 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | UBQLN4 | GRCh38.p7 | 1:156036200 | TGCCTAAAAGAGCTA[C/T]GAGTGCTTCTGCTCC | 56893 |
rs36006929 | snp | A/G | 0 | 0 | utr-variant-3-prime, nc-transcript-variant | UBQLN4 | GRCh38.p7 | 1:156036505 | CTCCTCCTTCAGAGC[A/G]AGAAATTCTAGCATT | 56893 |
rs36077783 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | UBQLN4 | GRCh38.p7 | 1:156036892 | AGAAGACGGAAGGGA[G/T]GACAAGCTGCAGAGG | 56893 |
rs36085345 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | UBQLN4 | GRCh38.p7 | 1:156035984 | TGAGGGGGGCTCAAA[C/T]TACTGGTGCCTGGGG | 56893 |
rs36120709 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | UBQLN4 | GRCh38.p7 | 1:156036356 | CCTGTCCAGAGAGCT[C/G]TCTCATCTCCCTCTT | 56893 |
rs41265003 | snp | C/T | 0.00874735 | 0.0655527 | utr-variant-3-prime, nc-transcript-variant | UBQLN4 | GRCh38.p7 | 1:156036111 | TGGCGCTTAGCTTCA[C/T]TGGGCTCCTTTTTTC | 56893 |
rs41265005 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | UBQLN4 | GRCh38.p7 | 1:156036154 | ATTAGCATCTCTAAG[C/T]CTCTTCTGCCAGCTC | 56893 |
rs41265007 | snp | A/G | 0.0692305 | 0.172692 | synonymous-codon, nc-transcript-variant | UBQLN4 | GRCh38.p7 | 1:156051288 | GGCAGGGTCAGGTGT[A/G]GAGGGGGAAGAAGCA | 56893 |
rs55757185 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | UBQLN4 | GRCh38.p7 | 1:156035766 | CCCAGCATCCAGAGC[C/T]CCAAGGGACCTAGCT | 56893 |
rs56681741 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | UBQLN4 | GRCh38.p7 | 1:156049851 | ACTGGGCCCTGCCCA[C/G]CCACAGTGCTCCCCA | 56893 |
rs58041058 | in-del | -/AAA | | | intron-variant | UBQLN4 | GRCh38.p7 | 1:156039958 | AAAAAAAAAAAAAAA[-/AAA]GACTCTTATAGCTAG | 56893 |
rs58044427 | snp | A/G/T | 0.0244538 | 0.107838 | intron-variant | UBQLN4 | GRCh38.p7 | 1:156040116 | AAGCCCTTTCTGGAC[A/G/T]GGTGTGGTGGCTCAC | 56893 |
rs58466287 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | UBQLN4 | GRCh38.p7 | 1:156037449 | AAATACAAAAAATTC[A/G]CTGGGTGTGGTGGTG | 56893 |
rs58657372 | in-del | -/AA | | | downstream-variant-500B | UBQLN4 | GRCh38.p7 | 1:156034873 | ATATATATATATAAT[-/AA]TTTTTTTTCTTTTGA | 56893 |
rs58858774 | snp | G/T | | | | | GRCh38.p7 | 1:156034678 | TAATCTTACAATTCA[G/T]TTTCCTCTACCACAC | 56893 |
rs59303673 | in-del | -/T/TT | 0.5 | 0 | | | GRCh38.p7 | 1:156034314 | TTTTTTTTTTTTTTT[-/T/TT]GAGACGGAGTCTTGC | 56893 |
rs59598606 | in-del | -/A | | | intron-variant | UBQLN4 | GRCh38.p7 | 1:156046558 | TTAAAAAAAAAAAAA[-/A]GCAGCCAAGTGCAGT | 56893 |
rs59781317 | snp | A/G | 0.462144 | 0.132269 | intron-variant | UBQLN4 | GRCh38.p7 | 1:156046565 | AAAAAAAAAGCAGCC[A/G]AGTGCAGTGGCTCAC | 56893 |
rs60215858 | in-del | -/TA/TATATAT | 0 | 0 | downstream-variant-500B | UBQLN4 | GRCh38.p7 | 1:156034871 | ATATATATATATATA[-/TA/TATATAT]ATTTTTTTTTCTTTT | 56893 |
rs61405654 | in-del | -/TATATATATATATA | | | downstream-variant-500B | UBQLN4 | GRCh38.p7 | 1:156034858 | ATATATATATATATA[-/TATATATATATATA]ATTTTTTTTTCTTTT | 56893 |
rs61813291 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | UBQLN4 | GRCh38.p7 | 1:156035391 | AGACATCTTCTCTGG[A/G]CTGCTTGGGACCCTT | 56893 |
rs61813292 | snp | A/C | | | intron-variant | UBQLN4 | GRCh38.p7 | 1:156045286 | TCACCTCACCAGATC[A/C]TGTTCAGATAACAGA | 56893 |
rs61813293 | snp | G/T | 0.0898077 | 0.191933 | intron-variant | UBQLN4 | GRCh38.p7 | 1:156049284 | CTGCAAGTTGGGGAA[G/T]GAAAGCGTTCAAGCT | 56893 |
rs62001917 | snp | A/G | 0.0123132 | 0.0774917 | synonymous-codon, nc-transcript-variant | UBQLN4 | GRCh38.p7 | 1:156041545 | GAGTTGCTGCTGGGC[A/G]CTGGAAGCCCCTGTT | 56893 |
rs62001918 | snp | G/T | 0.00813542 | 0.0632576 | missense, nc-transcript-variant | UBQLN4 | GRCh38.p7 | 1:156041636 | TTGCTGCCTGCTGAG[G/T]GTGCTGGGGTCCGGG | 56893 |
rs66667238 | in-del | -/TT | | | | | GRCh38.p7 | 1:156034313 | AGTTTTTGTTTTACT[-/TT]TTTTTTTTTTTTTTT | 56893 |
rs71630612 | snp | C/G | 0.5 | 0 | intron-variant | UBQLN4 | GRCh38.p7 | 1:156045025 | TCCCAAAGGCAACAC[C/G]GGAACCTCCTCCCCT | 56893 |
rs72708244 | snp | G/T | 0.00953873 | 0.0683987 | intron-variant | LOC105371729 | GRCh38.p7 | 1:156032734 | TCTCTGCGGCACTTC[G/T]CCTCTCCGCCAACGA | 56893 |
rs73004941 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | UBQLN4 | GRCh38.p7 | 1:156043580 | TCCAGATAAATGGAG[C/T]ATCCTCTAGGGTTGT | 56893 |
rs73004944 | snp | C/G | 0.00435825 | 0.0464772 | intron-variant | UBQLN4 | GRCh38.p7 | 1:156048701 | GCCCCGGAACCAGGG[C/G]AGCACCAACCTAGGA | 56893 |
rs74116473 | snp | A/G | 0.5 | 0 | intron-variant | UBQLN4 | GRCh38.p7 | 1:156043381 | TCATCCTGGAGATGA[A/G]GACCTTTCCAGGATG | 56893 |
rs74486399 | snp | A/C | 0.0811548 | 0.184367 | intron-variant | UBQLN4 | GRCh38.p7 | 1:156047920 | AAAAAGAAAGAAAGA[A/C]AGAACCAAAAGGGCA | 56893 |
rs74543372 | snp | C/T | 0.206947 | 0.246265 | intron-variant | UBQLN4 | GRCh38.p7 | 1:156046215 | GTTTTAGGCCGGGCA[C/T]GGTGGCTCACGCCTA | 56893 |
rs74548865 | snp | G/T | 0.5 | 0 | intron-variant | UBQLN4 | GRCh38.p7 | 1:156045863 | ATAATTTTTTTTTTT[G/T]GAGATGGAGTCTCGT | 56893 |
rs74593044 | snp | C/G | 0.0554779 | 0.157039 | intron-variant | UBQLN4 | GRCh38.p7 | 1:156047077 | AAATATTAAATATGT[C/G]TAGGAAAATAAACAA | 56893 |
rs75438798 | snp | C/G | 0.5 | 0 | intron-variant | UBQLN4 | GRCh38.p7 | 1:156039326 | CACGATCTCAGCTCA[C/G]TACAACCTCTGCCTC | 56893 |
rs75852693 | snp | A/T | 0.00914312 | 0.0669923 | downstream-variant-500B | LOC105371729 | GRCh38.p7 | 1:156033376 | CTGATGATTCCAGGT[A/T]TTTTTTGTTTTGTTT | 56893 |
rs76074057 | snp | G/T | 0.5 | 0 | intron-variant | UBQLN4 | GRCh38.p7 | 1:156045864 | TAATTTTTTTTTTTT[G/T]AGATGGAGTCTCGTT | 56893 |
rs76306768 | snp | C/T | | | upstream-variant-2KB | LAMTOR2, UBQLN4 | GRCh38.p7 | 1:156054409 | AGAGCCTTGGTTTCC[C/T]CAAGATAATAATAAT | 56893 |
rs76457408 | snp | G/T | 0 | 0 | intron-variant | UBQLN4 | GRCh38.p7 | 1:156047262 | TTTTTTTTTTTTTTT[G/T]AGATGGAGTCTCACT | 56893 |
rs76676776 | snp | C/T | 0.5 | 0 | utr-variant-3-prime, nc-transcript-variant | UBQLN4 | GRCh38.p7 | 1:156036219 | TGCTTCTGCTCCCCA[C/T]TGTTAATTCCAACTT | 56893 |
rs76830943 | snp | C/T | 0.431029 | 0.17242 | intron-variant | UBQLN4 | GRCh38.p7 | 1:156039336 | GCTCACTACAACCTC[C/T]GCCTCCCAGGTTCAA | 56893 |
rs76912290 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBQLN4 | GRCh38.p7 | 1:156047995 | ACAAAAAAAAAGAAT[A/G]TTACATTTTTATCTA | 56893 |
rs77660148 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | UBQLN4 | GRCh38.p7 | 1:156049674 | TGAACAAAACACTCA[A/C]AAGTCCTTGACCTTA | 56893 |
rs77735399 | snp | A/T | 0 | 0 | intron-variant | UBQLN4 | GRCh38.p7 | 1:156046544 | TTTTTAAAGGTTGTA[A/T]TAAAAAAAAAAAAAG | 56893 |
rs78344815 | snp | G/T | 0.5 | 0 | intron-variant | UBQLN4 | GRCh38.p7 | 1:156047260 | TTTTTTTTTTTTTTT[G/T]TGAGATGGAGTCTCA | 56893 |
rs78379095 | snp | C/G | 0.0327778 | 0.123752 | intron-variant | UBQLN4 | GRCh38.p7 | 1:156045232 | TGGGTCATGGGGACC[C/G]GGGCTAACCAAGGAT | 56893 |
rs78441735 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | UBQLN4 | GRCh38.p7 | 1:156044425 | GGAGCTAGCTGATGC[C/T]AGTGACTGGATAACT | 56893 |
rs78607985 | snp | G/T | 0.5 | 0 | | | GRCh38.p7 | 1:156034315 | TTTTTTTTTTTTTTT[G/T]AGACGGAGTCTTGCT | 56893 |
rs78720906 | snp | A/T | 0 | 0 | intron-variant | UBQLN4 | GRCh38.p7 | 1:156046546 | TTTAAAGGTTGTATT[A/T]AAAAAAAAAAAAGCA | 56893 |