SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs763874836 | snp | C/T | 1.84759e-05 | 0.00303935 | missense, upstream-variant-2KB | LAMTOR2, UBQLN4 | GRCh38.p7 | 1:156054936 | TAAGCCAAGCCAACA[C/T]TGGAGGCGTCCAGAG | 56893 |
rs763965814 | snp | C/T | | | intron-variant | UBQLN4 | GRCh38.p7 | 1:156039388 | CTCGAGTAGCTGGGA[C/T]GATAGGCATGCGCCA | 56893 |
rs764069060 | snp | C/G | 8.80863e-05 | 0.00663592 | upstream-variant-2KB, missense, nc-transcript-variant | LAMTOR2, UBQLN4 | GRCh38.p7 | 1:156053676 | CGAATGGGGGGCCTC[C/G]TCTCGGCCCCGCTCG | 56893 |
rs764213057 | snp | G/T | | | upstream-variant-2KB | LAMTOR2, UBQLN4 | GRCh38.p7 | 1:156054681 | CTATAATTCCCAGGG[G/T]GCCTCGCGAGGCCAC | 56893 |
rs764268537 | snp | C/T | 1.80266e-05 | 0.00300216 | intron-variant | UBQLN4 | GRCh38.p7 | 1:156050284 | TCTCCAGCCCTCTCA[C/T]ACTCACCTGCCTCAT | 56893 |
rs764281763 | in-del | -/A | | | upstream-variant-2KB | LAMTOR2, UBQLN4 | GRCh38.p7 | 1:156054542 | GAATCGTGGACTGCC[-/A]AAGCGGACACGTTGA | 56893 |
rs764282896 | snp | A/G | 1.6585e-05 | 0.00287962 | synonymous-codon, nc-transcript-variant | UBQLN4 | GRCh38.p7 | 1:156050504 | CAGCTCCATGAAGTT[A/G]GCAGAGCCCAGGCCT | 56893 |
rs764284845 | snp | A/G | 2.64722e-05 | 0.00363805 | synonymous-codon, nc-transcript-variant | UBQLN4 | GRCh38.p7 | 1:156041644 | TGCTGAGGGTGCTGG[A/G]GTCCGGGATATCCCA | 56893 |
rs764426295 | snp | A/G | 1.6477e-05 | 0.00287024 | missense, upstream-variant-2KB | LAMTOR2, UBQLN4 | GRCh38.p7 | 1:156055397 | CGTTTAATGAAGACA[A/G]TCTCAAATTCATCCT | 56893 |
rs764428859 | in-del | -/T | | | | | GRCh38.p7 | 1:156034171 | AAAGATAAAACCCCA[-/T]TAGGTGTGAAAAGAC | 56893 |
rs764515099 | snp | C/T | | | intron-variant | UBQLN4 | GRCh38.p7 | 1:156044815 | GGCACACCACAGTGG[C/T]GGCCCCTAGCAGAAC | 56893 |
rs764551389 | snp | C/G | 1.64781e-05 | 0.00287033 | missense, nc-transcript-variant | UBQLN4 | GRCh38.p7 | 1:156051712 | TGAACTTACTTCTGA[C/G]GGGTCTTGATGACCA | 56893 |
rs764771378 | snp | A/G | 3.29489e-05 | 0.00405874 | synonymous-codon, nc-transcript-variant | UBQLN4 | GRCh38.p7 | 1:156051728 | GGGTCTTGATGACCA[A/G]ATGGACAGTGAGCCC | 56893 |
rs764832350 | snp | A/G | 2.15274e-05 | 0.00328073 | missense, nc-transcript-variant | UBQLN4 | GRCh38.p7 | 1:156041612 | GGGGCCTCGGGCGTA[A/G]ACCCTGCGTTGCTGC | 56893 |
rs764861236 | snp | C/G | 1.66136e-05 | 0.00288211 | intron-variant | UBQLN4 | GRCh38.p7 | 1:156051889 | GAGGTCACTGTGGAG[C/G]CTGCCTGGACTCCCC | 56893 |
rs764951911 | snp | C/T | 1.80726e-05 | 0.00300599 | intron-variant | UBQLN4 | GRCh38.p7 | 1:156050244 | AGGCTGGGCAGGGCA[C/T]GGCTGGGCACCAGTG | 56893 |
rs765033224 | snp | C/T | 1.6591e-05 | 0.00288015 | missense, nc-transcript-variant | UBQLN4 | GRCh38.p7 | 1:156041546 | AGTTGCTGCTGGGCG[C/T]TGGAAGCCCCTGTTG | 56893 |
rs765034790 | snp | C/T | | | intron-variant | UBQLN4 | GRCh38.p7 | 1:156049165 | GCTCAGAGATGTTAA[C/T]TGACTTGCTGCCCTG | 56893 |
rs765073301 | snp | C/T | 4.95757e-05 | 0.00497849 | synonymous-codon, nc-transcript-variant | UBQLN4 | GRCh38.p7 | 1:156048657 | CCGAGCAAGCTCCAT[C/T]GTCTGATCAAGGGAG | 56893 |
rs765130263 | snp | A/G | | | intron-variant | UBQLN4 | GRCh38.p7 | 1:156037456 | AAAAATTCGCTGGGT[A/G]TGGTGGTGGGCGCCC | 56893 |
rs765191356 | in-del | -/GGAATTCA | | | intron-variant | UBQLN4 | GRCh38.p7 | 1:156049071 | GGCCAAGTAGCTTAC[-/GGAATTCA]GGAATTCAAGTCATG | 56893 |
rs765227929 | snp | C/T | 6.23189e-05 | 0.00558172 | intron-variant | UBQLN4 | GRCh38.p7 | 1:156051096 | AGATTGTGCTCTCCT[C/T]TCTGAGGGCTTACAG | 56893 |
rs765403017 | snp | A/T | 6.68293e-05 | 0.00578015 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | UBQLN4 | GRCh38.p7 | 1:156041913 | CTGCAAGGTCTGTAG[A/T]CCCTGCTGGATCTGC | 56893 |
rs765543518 | snp | C/T | 6.84756e-05 | 0.00585091 | synonymous-codon, nc-transcript-variant | UBQLN4 | GRCh38.p7 | 1:156050531 | GCCTAGGCTGCCCAG[C/T]CCCAGGATGCCCCCA | 56893 |
rs765632313 | in-del | -/TTTTTTT | | | intron-variant | UBQLN4 | GRCh38.p7 | 1:156040442 | ATCACAGTCCACACA[-/TTTTTTT]TTTTTTTTTTTTTTT | 56893 |
rs765641918 | snp | A/G | 3.41204e-05 | 0.00413026 | utr-variant-3-prime, nc-transcript-variant | UBQLN4 | GRCh38.p7 | 1:156036929 | ATTGACAGAAGAACC[A/G]AATGCTGACATCGAG | 56893 |
rs765711347 | snp | A/G | | | intron-variant | UBQLN4 | GRCh38.p7 | 1:156040975 | TTTGGTTACCTCGCA[A/G]AATCCCCCTCCCCAG | 56893 |
rs765843452 | snp | A/G | 2.29276e-05 | 0.00338575 | synonymous-codon, nc-transcript-variant | UBQLN4 | GRCh38.p7 | 1:156041620 | GGGCGTAGACCCTGC[A/G]TTGCTGCCTGCTGAG | 56893 |
rs765884220 | snp | A/G | 1.76173e-05 | 0.00296788 | missense, intron-variant | UBQLN4 | GRCh38.p7 | 1:156044045 | GGGTTCGAGACTGTC[A/G]GGTGCACCTGGCTGG | 56893 |
rs765905860 | snp | A/G | 3.46374e-05 | 0.00416143 | upstream-variant-2KB, missense, nc-transcript-variant | LAMTOR2, UBQLN4 | GRCh38.p7 | 1:156053619 | GAGGCTCGATCGCAG[A/G]TCACAATTTCCTCCT | 56893 |
rs765993695 | snp | C/T | 1.67559e-05 | 0.00289442 | intron-variant | UBQLN4 | GRCh38.p7 | 1:156051904 | GCTGCCTGGACTCCC[C/T]CTACCAGGGACCCTG | 56893 |
rs765996825 | snp | A/G | 0.000130399 | 0.00807358 | missense, intron-variant | UBQLN4 | GRCh38.p7 | 1:156044117 | TGGGAGGTGGGGGGC[A/G]AGGGGCTCCAGGGGT | 56893 |
rs766094535 | snp | A/G | 1.6759e-05 | 0.00289469 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | UBQLN4 | GRCh38.p7 | 1:156041874 | CCCCTACCCTCACCT[A/G]GGTACCAGCCCAGGG | 56893 |
rs766179199 | snp | A/G | 4.89584e-05 | 0.0049474 | missense, nc-transcript-variant | UBQLN4 | GRCh38.p7 | 1:156041630 | CCTGCGTTGCTGCCT[A/G]CTGAGGGTGCTGGGG | 56893 |
rs766265614 | snp | A/G | | | | | GRCh38.p7 | 1:156034092 | TATACCATTATCAAA[A/G]TGGAACCTCCCACTC | 56893 |
rs766351941 | snp | A/G | 1.66352e-05 | 0.00288398 | intron-variant | UBQLN4 | GRCh38.p7 | 1:156042728 | ACTGCCCCCAACCAA[A/G]AGGAACTCTCTCCCC | 56893 |
rs766383388 | snp | C/T | 1.8069e-05 | 0.00300569 | intron-variant | UBQLN4 | GRCh38.p7 | 1:156050254 | GGGCACGGCTGGGCA[C/T]CAGTGTCCTCCAGCT | 56893 |
rs766399102 | snp | C/T | 1.90856e-05 | 0.00308908 | synonymous-codon, upstream-variant-2KB | LAMTOR2, UBQLN4 | GRCh38.p7 | 1:156054952 | TGGAGGCGTCCAGAG[C/T]ACCCTGTGAGTGCAG | 56893 |
rs766560032 | snp | A/G | | | intron-variant | UBQLN4 | GRCh38.p7 | 1:156038102 | TTTTTTTGGCTGGGC[A/G]TAGTGGCTCATGCCT | 56893 |
rs766625825 | snp | G/T | 0.000118425 | 0.00769405 | synonymous-codon, nc-transcript-variant | UBQLN4 | GRCh38.p7 | 1:156051246 | GGCAGGGGTGGCGGG[G/T]GAAGCAGGCGTGGTG | 56893 |
rs766661490 | snp | C/G | 1.68394e-05 | 0.00290162 | missense, downstream-variant-500B, nc-transcript-variant | UBQLN4 | GRCh38.p7 | 1:156042156 | CTCCTCACTCACCTG[C/G]TGCAGGAAGACTGGG | 56893 |
rs766721655 | in-del | -/G | 5.98426e-05 | 0.00546971 | upstream-variant-2KB, frameshift-variant, nc-transcript-variant | LAMTOR2, UBQLN4 | GRCh38.p7 | 1:156053665 | GACGGTGACCCGAAT[-/G]GGGGGGCCTCGTCTC | 56893 |
rs766824603 | snp | C/T | 1.64773e-05 | 0.00287026 | missense, nc-transcript-variant | UBQLN4 | GRCh38.p7 | 1:156037085 | TGAAGCCCATGGAGT[C/T]GAGCTGCTCCAGCTG | 56893 |
rs766921515 | snp | C/T | 0.000234734 | 0.0108311 | utr-variant-3-prime, nc-transcript-variant | UBQLN4 | GRCh38.p7 | 1:156036966 | GAGAGGCAGGAGGCA[C/T]GGGCCGAGGGATTAG | 56893 |
rs766957258 | snp | A/G | 1.70064e-05 | 0.00291597 | utr-variant-3-prime, nc-transcript-variant | UBQLN4 | GRCh38.p7 | 1:156036942 | CCGAATGCTGACATC[A/G]AGGGAGGGGAGAGGC | 56893 |
rs767041457 | snp | A/T | | | nc-transcript-variant | LOC105371729 | GRCh38.p7 | 1:156032829 | GGATTCCCCCAAGGA[A/T]GAAGATCCCAGCCTT | 56893 |
rs767056247 | snp | C/T | 1.65274e-05 | 0.00287462 | synonymous-codon, nc-transcript-variant | UBQLN4 | GRCh38.p7 | 1:156037116 | CTGCTGAAATCTCAC[C/T]TCTGGCGTCTGCACC | 56893 |
rs767117977 | snp | A/G | 4.39396e-05 | 0.00468699 | synonymous-codon, intron-variant | UBQLN4 | GRCh38.p7 | 1:156044131 | CGAGGGGCTCCAGGG[A/G]TTAGGGAGGGGCTCT | 56893 |
rs767197988 | snp | C/G | 1.80344e-05 | 0.00300281 | missense, upstream-variant-2KB | LAMTOR2, UBQLN4 | GRCh38.p7 | 1:156054912 | GCCCCAAGGCTTTGA[C/G]CCAGGTGCTAAGCCA | 56893 |
rs767326644 | snp | C/T | 4.07357e-05 | 0.00451289 | upstream-variant-2KB, missense, nc-transcript-variant | LAMTOR2, UBQLN4 | GRCh38.p7 | 1:156053640 | ATTTCCTCCTTGTCC[C/T]TGGGGGTCTTGACGG | 56893 |
rs767398769 | snp | C/G/T | 3.33886e-05 | 0.00408575 | intron-variant, downstream-variant-500B | UBQLN4 | GRCh38.p7 | 1:156042126 | CCCCTTGCCCTCAAC[C/G/T]TCCACCCATCTAGGC | 56893 |
rs767622665 | in-del | -/A | | | intron-variant | UBQLN4 | GRCh38.p7 | 1:156046334 | CTCTACTAATAATAC[-/A]AAAAAAAAAAAAAAA | 56893 |
rs767635940 | snp | C/G | 0.000165544 | 0.0090964 | intron-variant, upstream-variant-2KB | LAMTOR2, UBQLN4 | GRCh38.p7 | 1:156055254 | CTATCCCTCCCCGCC[C/G]CTCACCAGGCTGCTG | 56893 |
rs767688742 | snp | A/G | 1.66244e-05 | 0.00288304 | missense, nc-transcript-variant | UBQLN4 | GRCh38.p7 | 1:156042868 | AGCTGGGGGTTCTCA[A/G]AGATCTGCTGGAGGA | 56893 |
rs767766012 | snp | C/T | | | intron-variant | UBQLN4 | GRCh38.p7 | 1:156044892 | CAAACCCTACCTCTA[C/T]ACACTGGCTACTTCA | 56893 |
rs767778977 | snp | C/T | | | intron-variant | UBQLN4 | GRCh38.p7 | 1:156037810 | CTCCAAGGCCCCTCC[C/T]AATAGTCATCACACG | 56893 |
rs767813808 | in-del | -/A | | | intron-variant | UBQLN4 | GRCh38.p7 | 1:156045773 | GTAAAACAAGTCCAT[-/A]CTTTCCTCTACAGTT | 56893 |
rs767885480 | snp | C/T | 1.66056e-05 | 0.00288141 | intron-variant | UBQLN4 | GRCh38.p7 | 1:156042743 | GAGGAACTCTCTCCC[C/T]AACAATACTCTCCTC | 56893 |
rs767941626 | snp | C/T | 1.64808e-05 | 0.00287057 | intron-variant | UBQLN4 | GRCh38.p7 | 1:156051697 | GATCTGCTCTGCTCC[C/T]GAACTTACTTCTGAG | 56893 |
rs768026557 | snp | C/T | | | intron-variant | UBQLN4 | GRCh38.p7 | 1:156038247 | CCAGGTGTGGTGGCG[C/T]ATGCCTGTAGTCCCA | 56893 |
rs768034020 | snp | C/T | 1.64985e-05 | 0.0028721 | intron-variant, upstream-variant-2KB | LAMTOR2, UBQLN4 | GRCh38.p7 | 1:156055451 | GGGAGCCAGACTTCC[C/T]CTGTCCCCCAAAGGG | 56893 |
rs768065067 | snp | C/G | 7.47929e-05 | 0.00611481 | intron-variant, synonymous-codon, nc-transcript-variant | UBQLN4 | GRCh38.p7 | 1:156051150 | GGATCCCTCCCCAGC[C/G]CCCGGAGAGGGCCCC | 56893 |
rs768138962 | snp | A/C | 5.19728e-05 | 0.00509742 | intron-variant | UBQLN4 | GRCh38.p7 | 1:156048706 | GGAACCAGGGGAGCA[A/C]CAACCTAGGAAAAGG | 56893 |
rs768155341 | snp | C/T | 1.65228e-05 | 0.00287422 | synonymous-codon, nc-transcript-variant | UBQLN4 | GRCh38.p7 | 1:156050390 | AATCATGTGACGCAT[C/T]AGATCAGGGTTAGAC | 56893 |
rs768254635 | snp | C/G | | | upstream-variant-2KB, intron-variant | LAMTOR2, UBQLN4 | GRCh38.p7 | 1:156052777 | AAATTCAGCTTTGTA[C/G]GGAACATACAGTATT | 56893 |
rs768271481 | in-del | -/AC | | | | | GRCh38.p7 | 1:156034294 | AAGAGTTTTTGTTTT[-/AC]ACTTTTTTTTTTTTT | 56893 |
rs768289313 | snp | A/C | | | utr-variant-5-prime, upstream-variant-2KB | LAMTOR2, UBQLN4 | GRCh38.p7 | 1:156054796 | CAGGGCGTCCCGGAG[A/C]AGGCCAACGGGACTA | 56893 |
rs768338114 | in-del | -/GGGGGCAGC | | | intron-variant, upstream-variant-2KB | LAMTOR2, UBQLN4 | GRCh38.p7 | 1:156055064 | GGAGGAAGCGGCAGA[-/GGGGGCAGC]GGCTGGGGATACCGG | 56893 |
rs768393528 | snp | C/T | 1.6483e-05 | 0.00287076 | synonymous-codon, upstream-variant-2KB | LAMTOR2, UBQLN4 | GRCh38.p7 | 1:156055326 | CACTGACGCCCGGGT[C/T]ACCGCTGCCATAGCC | 56893 |
rs768434487 | snp | C/T | 9.12034e-05 | 0.00675229 | missense, nc-transcript-variant | UBQLN4 | GRCh38.p7 | 1:156051322 | GCAGCAGCTGGATCT[C/T]GAGCCCTGAGGACAG | 56893 |
rs768459967 | snp | C/G/T | 3.31913e-05 | 0.00407367 | intron-variant, upstream-variant-2KB | LAMTOR2, UBQLN4 | GRCh38.p7 | 1:156055238 | CGCTCTGAGCACATC[C/G/T]CTATCCCTCCCCGCC | 56893 |
rs768595906 | snp | C/T | 1.94252e-05 | 0.00311644 | intron-variant, utr-variant-3-prime | UBQLN4 | GRCh38.p7 | 1:156042279 | ACCTGGGCCTTTTCA[C/T]CCTAAGAATTCCCCC | 56893 |
rs768664254 | snp | C/T | | | intron-variant | UBQLN4 | GRCh38.p7 | 1:156043619 | TAACCTGTTCTTCTG[C/T]ACATGGCAAGCCCTG | 56893 |
rs768692380 | in-del | -/CCCCACTT | 1.97089e-05 | 0.00313912 | frameshift-variant, nc-transcript-variant | UBQLN4 | GRCh38.p7 | 1:156041600 | GTGAGGAAGTGGGGG[-/CCCCACTT]CCTCGGGCGTAGACC | 56893 |
rs768752076 | snp | A/C | | | missense, downstream-variant-500B, nc-transcript-variant | UBQLN4 | GRCh38.p7 | 1:156042189 | CTGCAGGCGGAGCTG[A/C]TCCTGCAGTTGGGGG | 56893 |
rs768757280 | snp | A/G | 8.26822e-05 | 0.00642917 | synonymous-codon, intron-variant | UBQLN4 | GRCh38.p7 | 1:156044185 | GGAGGATGAGCTGTC[A/G]GAGTTCCCGGCCAGG | 56893 |
rs768849246 | snp | A/G | 1.64754e-05 | 0.00287009 | synonymous-codon, nc-transcript-variant | UBQLN4 | GRCh38.p7 | 1:156037052 | CAATCAGGGCCTGCA[A/G]GTTAGCCTCACGATT | 56893 |
rs768914927 | snp | C/T | 7.01139e-05 | 0.00592048 | upstream-variant-2KB, missense, nc-transcript-variant | LAMTOR2, UBQLN4 | GRCh38.p7 | 1:156053602 | GTACTACCTCCTTGA[C/T]CGAGGCTCGATCGCA | 56893 |
rs768944419 | snp | G/T | | | intron-variant | UBQLN4 | GRCh38.p7 | 1:156051385 | AAGAGGGAAGGTACC[G/T]TGACAATCTCTGTGC | 56893 |
rs769053520 | snp | A/G | 1.64953e-05 | 0.00287182 | missense, nc-transcript-variant | UBQLN4 | GRCh38.p7 | 1:156051839 | GAGCCTTAAACCTCC[A/G]GGAGATTTCCTCTTT | 56893 |
rs769077828 | snp | C/G | | | | | GRCh38.p7 | 1:156033629 | TGTCAGATCACCTGA[C/G]GTCAGAAGTTCGAGA | 56893 |
rs769160418 | snp | C/T | | | intron-variant | UBQLN4 | GRCh38.p7 | 1:156047755 | AAAAAGTTAGCCGGG[C/T]GTGGTGGCATGTACC | 56893 |
rs769168300 | snp | A/C | 2.03722e-05 | 0.0031915 | intron-variant | UBQLN4 | GRCh38.p7 | 1:156050585 | GGGTCACAGTCTGCC[A/C]CAAGAACAGTGTCCT | 56893 |
rs769198996 | snp | A/T | | | intron-variant | UBQLN4 | GRCh38.p7 | 1:156041708 | AGGTAGGAGATGGCA[A/T]CCAAGAAAGGGATGA | 56893 |
rs769267677 | snp | C/T | 6.85448e-05 | 0.00585386 | intron-variant, downstream-variant-500B | UBQLN4 | GRCh38.p7 | 1:156041857 | CTTGCTGCCCTCCTG[C/T]CCCCCTACCCTCACC | 56893 |
rs769444168 | snp | A/G | 3.29554e-05 | 0.00405914 | synonymous-codon, nc-transcript-variant | UBQLN4 | GRCh38.p7 | 1:156050435 | CAGGGGGTTCTCCAT[A/G]ATCTGTGACAGCATC | 56893 |
rs769471045 | snp | A/G | 1.6476e-05 | 0.00287014 | missense, upstream-variant-2KB | LAMTOR2, UBQLN4 | GRCh38.p7 | 1:156055367 | GGGCCGCCTACGACC[A/G]GAACGGGAACCAAGC | 56893 |
rs769534848 | snp | A/T | | | intron-variant | UBQLN4 | GRCh38.p7 | 1:156050940 | ACCTCTGAGAACTCC[A/T]CAGACTAGTTTCTTC | 56893 |
rs769573635 | snp | G/T | 1.97478e-05 | 0.00314222 | intron-variant | UBQLN4 | GRCh38.p7 | 1:156043953 | TCCTGGGACAGAGGG[G/T]CTGCCCTGGTGACCC | 56893 |
rs769602433 | in-del | -/AC | | | intron-variant | UBQLN4 | GRCh38.p7 | 1:156040039 | CGATCCAGAGAAAAG[-/AC]AGGACTTGCCTGGGG | 56893 |
rs769642365 | snp | A/C/T | 4.95138e-05 | 0.00497543 | intron-variant, upstream-variant-2KB | LAMTOR2, UBQLN4 | GRCh38.p7 | 1:156055458 | AGACTTCCCCTGTCC[A/C/T]CCAAAGGGGATCCCA | 56893 |
rs769727266 | snp | A/G | | | intron-variant | UBQLN4 | GRCh38.p7 | 1:156039144 | AGACTGGGTCTCCCC[A/G]CGTTGCCCAGGCTGG | 56893 |
rs769862667 | snp | A/T | | | intron-variant | UBQLN4 | GRCh38.p7 | 1:156045750 | ACATCAAAGAGAACT[A/T]CAAAAATGTAAAACA | 56893 |
rs769863790 | snp | A/G | 1.64749e-05 | 0.00287005 | missense, nc-transcript-variant | UBQLN4 | GRCh38.p7 | 1:156037064 | GCAGGTTAGCCTCAC[A/G]ATTGATGAAGCCCAT | 56893 |
rs769893585 | in-del | -/CA | 1.94797e-05 | 0.00312081 | intron-variant | UBQLN4 | GRCh38.p7 | 1:156050574 | GGAAGGGGGCAGGGT[-/CA]CAGTCTGCCACAAGA | 56893 |
rs769929542 | snp | C/T | 2.39426e-05 | 0.00345988 | missense, nc-transcript-variant | UBQLN4 | GRCh38.p7 | 1:156051212 | CATCTGAAGAGGCAC[C/T]GCCAGAGGTGGAGGG | 56893 |
rs770071003 | snp | A/T | | | intron-variant | UBQLN4 | GRCh38.p7 | 1:156037155 | ACAGGCCTTGTGAAG[A/T]GGGCACAGGACCAAT | 56893 |
rs770266985 | snp | C/G | 3.03633e-05 | 0.00389625 | synonymous-codon, intron-variant | UBQLN4 | GRCh38.p7 | 1:156044110 | GGGGGCCTGGGAGGT[C/G]GGGGGCGAGGGGCTC | 56893 |
rs770283478 | snp | G/T | 8.87351e-05 | 0.00666031 | missense, intron-variant | UBQLN4 | GRCh38.p7 | 1:156044211 | CCAGGGAAGAGAAGG[G/T]ATTGTTGCCAAACTG | 56893 |
rs770300068 | snp | C/T | | | intron-variant | UBQLN4 | GRCh38.p7 | 1:156052625 | CACCACGCCCAGCCG[C/T]ATCTCCATTTTAAAG | 56893 |
rs770317400 | snp | A/G | 1.72943e-05 | 0.00294055 | missense, downstream-variant-500B, nc-transcript-variant | UBQLN4 | GRCh38.p7 | 1:156042211 | AGTTGGGGGTTCCCC[A/G]CGAAGAGCGGCACAT | 56893 |
rs770364103 | snp | A/G | 7.36363e-05 | 0.00606735 | utr-variant-5-prime, upstream-variant-2KB | LAMTOR2, UBQLN4 | GRCh38.p7 | 1:156054884 | CCAGGGTTAGGAACC[A/G]TAGGCATGCTGCGCC | 56893 |
rs770371494 | snp | C/T | | | | | GRCh38.p7 | 1:156033473 | CTTGCTCCTTCCTTC[C/T]TTGCTTGACCCCAGG | 56893 |
rs770459405 | snp | A/G | 0.00013849 | 0.0083202 | upstream-variant-2KB, missense, nc-transcript-variant | LAMTOR2, UBQLN4 | GRCh38.p7 | 1:156053607 | ACCTCCTTGACCGAG[A/G]CTCGATCGCAGATCA | 56893 |
rs770493883 | snp | C/T | | | intron-variant | LOC105371729 | GRCh38.p7 | 1:156032635 | TCTTCCGGGCCAGGA[C/T]AGTGTTTTTTAACCT | 56893 |
rs770841312 | snp | C/T | 1.65201e-05 | 0.00287398 | synonymous-codon, nc-transcript-variant | UBQLN4 | GRCh38.p7 | 1:156050489 | CTGCATCTGCTGCTG[C/T]AGCTCCATGAAGTTG | 56893 |
rs770857838 | snp | A/C/G | 4.71868e-05 | 0.00485712 | intron-variant | UBQLN4 | GRCh38.p7 | 1:156051079 | CTCCCCAACCCCAAA[A/C/G]AAGATTGTGCTCTCC | 56893 |
rs771005659 | snp | A/G | 1.64732e-05 | 0.0028699 | synonymous-codon, nc-transcript-variant | UBQLN4 | GRCh38.p7 | 1:156051771 | GTGCTGGTTCAGTGT[A/G]TCCCCATCCTTGAGG | 56893 |
rs771051617 | snp | C/T | 1.65551e-05 | 0.00287702 | missense, nc-transcript-variant | UBQLN4 | GRCh38.p7 | 1:156042849 | TGAGATCACATTCTG[C/T]ATCAGCTGGGGGTTC | 56893 |
rs771307070 | snp | C/T | 4.95168e-05 | 0.00497553 | missense, nc-transcript-variant | UBQLN4 | GRCh38.p7 | 1:156048562 | ATGCGGCGGAGGGCA[C/T]TATACCCTCCAGGGA | 56893 |
rs771487205 | snp | A/G | 1.64876e-05 | 0.00287116 | intron-variant | UBQLN4 | GRCh38.p7 | 1:156041465 | GTGCTCCCAGCACCT[A/G]CCCCCACTGCCTCAT | 56893 |
rs771488654 | snp | C/T | 1.64868e-05 | 0.00287109 | missense, nc-transcript-variant | UBQLN4 | GRCh38.p7 | 1:156048578 | TATACCCTCCAGGGA[C/T]GCTCTCAAGGTTGCT | 56893 |
rs771503960 | snp | C/T | | | intron-variant | UBQLN4 | GRCh38.p7 | 1:156052400 | GGTGCGATCTTGGCT[C/T]ACTGTAACCTCCATC | 56893 |
rs771557669 | snp | C/G | 1.66054e-05 | 0.00288139 | intron-variant, upstream-variant-2KB | LAMTOR2, UBQLN4 | GRCh38.p7 | 1:156055231 | TACTCCCCGCTCTGA[C/G]CACATCGCTATCCCT | 56893 |
rs771607951 | snp | A/G | | | intron-variant | UBQLN4 | GRCh38.p7 | 1:156050275 | TCCTCCAGCTCTCCA[A/G]CCCTCTCATACTCAC | 56893 |
rs771662025 | snp | A/C | | | | | GRCh38.p7 | 1:156033794 | GGTTGCAGTGAGCCG[A/C]GATTGCATCACTGCA | 56893 |
rs771710660 | in-del | -/GAG | | | intron-variant | UBQLN4 | GRCh38.p7 | 1:156042469 | GGGTCTGATGATGAT[-/GAG]GACAGCTAACATTTC | 56893 |
rs771733811 | snp | A/G | | | upstream-variant-2KB, intron-variant | LAMTOR2, UBQLN4 | GRCh38.p7 | 1:156053223 | CTGAGGCACAGAGTA[A/G]GCGCCGGCGCTCTCC | 56893 |
rs771849608 | in-del | -/TTTTT | | | intron-variant | UBQLN4 | GRCh38.p7 | 1:156040444 | CACAGTCCACACATT[-/TTTTT]TTTTTTTTTTTTTTT | 56893 |
rs771977978 | snp | A/G | 0.000255075 | 0.0112904 | missense, nc-transcript-variant | UBQLN4 | GRCh38.p7 | 1:156051196 | CGGCTTCCACTGCCA[A/G]CATCTGAAGAGGCAC | 56893 |
rs771996560 | snp | C/G | 1.7896e-05 | 0.00299126 | intron-variant, utr-variant-3-prime | UBQLN4 | GRCh38.p7 | 1:156042244 | ACCATCATCTGCCAG[C/G]GTGAAGGTAGCAGGG | 56893 |
rs772096637 | snp | A/G | 2.27726e-05 | 0.00337428 | intron-variant | UBQLN4 | GRCh38.p7 | 1:156051086 | ACCCCAAACAAGATT[A/G]TGCTCTCCTCTCTGA | 56893 |
rs772116394 | snp | C/T | | | intron-variant | UBQLN4 | GRCh38.p7 | 1:156045390 | CCTAGCACCTCACCC[C/T]ACCTTGTTCTGGGCT | 56893 |
rs772117671 | snp | A/T | 3.90877e-05 | 0.00442067 | intron-variant | UBQLN4 | GRCh38.p7 | 1:156043963 | GAGGGGCTGCCCTGG[A/T]GACCCCACTAAGCTC | 56893 |
rs772144716 | snp | C/G | 3.29516e-05 | 0.00405891 | missense, nc-transcript-variant | UBQLN4 | GRCh38.p7 | 1:156051809 | CTGCGAAGATCAGGA[C/G]CAGCTGATCCTGCTG | 56893 |
rs772206426 | snp | A/T | | | intron-variant | UBQLN4 | GRCh38.p7 | 1:156050027 | AGGGTCAGGAGCTCT[A/T]CTCTATGCTCCTAGA | 56893 |
rs772207254 | snp | A/G | 6.34176e-05 | 0.0056307 | synonymous-codon, intron-variant | UBQLN4 | GRCh38.p7 | 1:156044089 | GGTGCCCTCCCCACC[A/G]GACCCGGGGGCCTGG | 56893 |
rs772417903 | snp | A/C | | | intron-variant | UBQLN4 | GRCh38.p7 | 1:156048387 | CTTCAAGCCAAGGCC[A/C]ACCCCTCAGGGGACT | 56893 |
rs772451548 | snp | C/T | | | missense, nc-transcript-variant | UBQLN4 | GRCh38.p7 | 1:156041595 | TGGCTGGTGAGGAAG[C/T]GGGGGCCTCGGGCGT | 56893 |
rs772582187 | snp | A/G | 1.71073e-05 | 0.00292461 | intron-variant | UBQLN4 | GRCh38.p7 | 1:156048699 | GGGCCCCGGAACCAG[A/G]GGAGCACCAACCTAG | 56893 |
rs772711862 | snp | A/C | 1.64776e-05 | 0.00287028 | missense, nc-transcript-variant | UBQLN4 | GRCh38.p7 | 1:156050438 | GGGGTTCTCCATGAT[A/C]TGTGACAGCATCTCA | 56893 |
rs772714956 | snp | A/G | 1.67416e-05 | 0.00289318 | intron-variant, downstream-variant-500B | UBQLN4 | GRCh38.p7 | 1:156042004 | TGGTGGGAAATAAGC[A/G]GAGAAAGGCATCAAG | 56893 |
rs772749860 | snp | A/G | 1.65888e-05 | 0.00287996 | intron-variant, upstream-variant-2KB | LAMTOR2, UBQLN4 | GRCh38.p7 | 1:156055241 | TCTGAGCACATCGCT[A/G]TCCCTCCCCGCCCCT | 56893 |
rs772884915 | snp | C/G | | | intron-variant | UBQLN4 | GRCh38.p7 | 1:156037200 | TTGAATTAAGGGTTT[C/G]TAAGACCAGCAGGTC | 56893 |
rs773006334 | snp | A/G/T | 3.61417e-05 | 0.00425086 | intron-variant | UBQLN4 | GRCh38.p7 | 1:156050245 | GGCTGGGCAGGGCAC[A/G/T]GCTGGGCACCAGTGT | 56893 |
rs773113893 | snp | A/G | 3.24018e-05 | 0.0040249 | missense, nc-transcript-variant | UBQLN4 | GRCh38.p7 | 1:156051238 | GAGGGCTGGGCAGGG[A/G]TGGCGGGTGAAGCAG | 56893 |
rs773285656 | snp | C/T | 1.64757e-05 | 0.00287012 | synonymous-codon, upstream-variant-2KB | LAMTOR2, UBQLN4 | GRCh38.p7 | 1:156055371 | CGCCTACGACCGGAA[C/T]GGGAACCAAGCGTTT | 56893 |
rs773394414 | snp | A/T | 5.11191e-05 | 0.00505539 | utr-variant-3-prime, nc-transcript-variant | UBQLN4 | GRCh38.p7 | 1:156036937 | AAGAACCGAATGCTG[A/T]CATCGAGGGAGGGGA | 56893 |
rs773649656 | snp | A/G | 1.98821e-05 | 0.00315288 | intron-variant | UBQLN4 | GRCh38.p7 | 1:156048450 | CTGGGGTGGGGGTAG[A/G]GAATCTCGAGCCCAG | 56893 |
rs773660903 | snp | G/T | 6.58979e-05 | 0.00573974 | missense, nc-transcript-variant | UBQLN4 | GRCh38.p7 | 1:156037067 | GGTTAGCCTCACGAT[G/T]GATGAAGCCCATGGA | 56893 |
rs773679516 | in-del | -/CC | 2.15492e-05 | 0.0032824 | intron-variant | UBQLN4 | GRCh38.p7 | 1:156051093 | ACAAGATTGTGCTCT[-/CC]TCTCTGAGGGCTTAC | 56893 |
rs773825785 | in-del | -/C | | | intron-variant | UBQLN4 | GRCh38.p7 | 1:156040148 | CCTATAATCCCAGCA[-/C]TTTGGGAGCCCGAGG | 56893 |
rs773829337 | snp | C/T | 3.45405e-05 | 0.00415561 | upstream-variant-2KB, missense, nc-transcript-variant | LAMTOR2, UBQLN4 | GRCh38.p7 | 1:156053610 | TCCTTGACCGAGGCT[C/T]GATCGCAGATCACAA | 56893 |
rs773866905 | snp | A/G | 5.49848e-05 | 0.00524303 | utr-variant-5-prime, upstream-variant-2KB | LAMTOR2, UBQLN4 | GRCh38.p7 | 1:156054887 | GGGTTAGGAACCGTA[A/G]GCATGCTGCGCCCCA | 56893 |
rs773882741 | snp | C/G | 3.76839e-05 | 0.00434057 | upstream-variant-2KB, missense, nc-transcript-variant | LAMTOR2, UBQLN4 | GRCh38.p7 | 1:156053633 | GATCACAATTTCCTC[C/G]TTGTCCTTGGGGGTC | 56893 |
rs773907701 | snp | A/G | | | utr-variant-5-prime, upstream-variant-2KB | LAMTOR2, UBQLN4 | GRCh38.p7 | 1:156054867 | GATCTGGGTGCAAAA[A/G]CCCAGGGTTAGGAAC | 56893 |
rs773919483 | snp | A/G | 3.13603e-05 | 0.00395969 | missense, intron-variant | UBQLN4 | GRCh38.p7 | 1:156044115 | CCTGGGAGGTGGGGG[A/G]CGAGGGGCTCCAGGG | 56893 |
rs774046653 | snp | C/G | 3.33211e-05 | 0.0040816 | intron-variant, downstream-variant-500B | UBQLN4 | GRCh38.p7 | 1:156042033 | AGAGGTGGCAGGAAA[C/G]AGGAGACAACCTCAA | 56893 |
rs774054171 | snp | A/G | | | intron-variant | LOC105371729 | GRCh38.p7 | 1:156032745 | CTTCGCCTCTCCGCC[A/G]ACGACAGAGGCGAAG | 56893 |
rs774224457 | snp | A/G | | | intron-variant | UBQLN4 | GRCh38.p7 | 1:156048060 | CATTTTTAAAAGTGT[A/G]TAATCCTGGGGCCCA | 56893 |
rs774359915 | snp | C/T | 1.65611e-05 | 0.00287755 | missense, nc-transcript-variant | UBQLN4 | GRCh38.p7 | 1:156042851 | AGATCACATTCTGCA[C/T]CAGCTGGGGGTTCTC | 56893 |
rs774409644 | snp | A/C | 6.60273e-05 | 0.00574537 | intron-variant, upstream-variant-2KB | LAMTOR2, UBQLN4 | GRCh38.p7 | 1:156055462 | TTCCCCTGTCCCCCA[A/C]AGGGGATCCCAAGGG | 56893 |
rs774447752 | snp | A/G | 5.91127e-05 | 0.00543625 | intron-variant | UBQLN4 | GRCh38.p7 | 1:156043956 | TGGGACAGAGGGGCT[A/G]CCCTGGTGACCCCAC | 56893 |
rs774624987 | snp | C/T | 1.65004e-05 | 0.00287227 | intron-variant | UBQLN4 | GRCh38.p7 | 1:156051672 | GATGGGGAGGCCCAA[C/T]CAGAAGCTGGATCTG | 56893 |
rs774634225 | snp | A/G | | | | | GRCh38.p7 | 1:156033641 | TGAGGTCAGAAGTTC[A/G]AGACCAGCCTGGCCA | 56893 |
rs774648397 | in-del | -/GCCCGCCCGGCTCCTCCTCCTCCCC | 0.00277392 | 0.0371385 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | LAMTOR2, UBQLN4 | GRCh38.p7 | 1:156053729 | CCCGGCCGCCCGCCA[-/GCCCGCCCGGCTCCTCCTCCTCCCC]GCCCGCCCGGCTCCT | 56893 |
rs774781380 | snp | A/G | 1.65021e-05 | 0.00287241 | synonymous-codon, nc-transcript-variant | UBQLN4 | GRCh38.p7 | 1:156048564 | GCGGCGGAGGGCATT[A/G]TACCCTCCAGGGATG | 56893 |
rs774787959 | snp | C/T | 1.81033e-05 | 0.00300854 | intron-variant | UBQLN4 | GRCh38.p7 | 1:156041469 | TCCCAGCACCTGCCC[C/T]CACTGCCTCATGTAC | 56893 |
rs775007595 | snp | C/G | 1.64814e-05 | 0.00287061 | synonymous-codon, nc-transcript-variant | UBQLN4 | GRCh38.p7 | 1:156048594 | GCTCTCAAGGTTGCT[C/G]AGGGCCCGGTCCTGG | 56893 |
rs775053458 | snp | C/T | 1.64811e-05 | 0.00287059 | missense, nc-transcript-variant | UBQLN4 | GRCh38.p7 | 1:156037090 | CCCATGGAGTTGAGC[C/T]GCTCCAGCTGCTGCT | 56893 |
rs775095748 | snp | A/G | 1.79005e-05 | 0.00299164 | intron-variant | UBQLN4 | GRCh38.p7 | 1:156041479 | TGCCCCCACTGCCTC[A/G]TGTACCTGTGAGTTT | 56893 |
rs775101624 | snp | C/T | | | intron-variant | UBQLN4 | GRCh38.p7 | 1:156047808 | AAGGCAGGAGAATTG[C/T]TTGAACCCGGGAGGC | 56893 |
rs775103008 | snp | A/G | 1.80497e-05 | 0.00300409 | synonymous-codon, upstream-variant-2KB | LAMTOR2, UBQLN4 | GRCh38.p7 | 1:156054916 | CAAGGCTTTGACCCA[A/G]GTGCTAAGCCAAGCC | 56893 |
rs775120221 | snp | A/G | | | intron-variant, downstream-variant-500B | UBQLN4 | GRCh38.p7 | 1:156041802 | AAGGATGCTGAGAGA[A/G]TGGCAGAGAGAAGAG | 56893 |
rs775191384 | snp | A/G | 1.65976e-05 | 0.00288072 | intron-variant, upstream-variant-2KB | LAMTOR2, UBQLN4 | GRCh38.p7 | 1:156055235 | CCCCGCTCTGAGCAC[A/G]TCGCTATCCCTCCCC | 56893 |
rs775261152 | snp | A/C | 8.89067e-05 | 0.00666674 | intron-variant | UBQLN4 | GRCh38.p7 | 1:156051089 | CCAAACAAGATTGTG[A/C]TCTCCTCTCTGAGGG | 56893 |
rs775290643 | snp | C/T | | | intron-variant | UBQLN4 | GRCh38.p7 | 1:156039163 | TGCCCAGGCTGGTCT[C/T]GAACTCCTGGCCTCA | 56893 |
rs775302623 | snp | C/G | | | intron-variant | UBQLN4 | GRCh38.p7 | 1:156037486 | CTGTAGTCCCAGCTA[C/G]TCAGGAGGCTGAGGC | 56893 |
rs775366894 | snp | G/T | 1.86221e-05 | 0.00305135 | intron-variant, utr-variant-3-prime | UBQLN4 | GRCh38.p7 | 1:156042260 | GTGAAGGTAGCAGGG[G/T]GAGACCTGGGCCTTT | 56893 |
rs775413580 | snp | A/G | | | intron-variant | UBQLN4 | GRCh38.p7 | 1:156044625 | TGCACCCCCAGCCCC[A/G]ACACTAGTAGGTGCT | 56893 |
rs775562211 | snp | A/G | 4.39686e-05 | 0.00468854 | missense, nc-transcript-variant | UBQLN4 | GRCh38.p7 | 1:156051202 | CCACTGCCAGCATCT[A/G]AAGAGGCACTGCCAG | 56893 |
rs775659918 | snp | C/T | 5.00279e-05 | 0.00500115 | synonymous-codon, nc-transcript-variant | UBQLN4 | GRCh38.p7 | 1:156042876 | GTTCTCAGAGATCTG[C/T]TGGAGGAGGGCTTGC | 56893 |
rs775669010 | snp | C/T | 1.64789e-05 | 0.0028704 | missense, nc-transcript-variant | UBQLN4 | GRCh38.p7 | 1:156051706 | TGCTCCTGAACTTAC[C/T]TCTGAGGGGTCTTGA | 56893 |
rs775762728 | snp | A/G | | | intron-variant | UBQLN4 | GRCh38.p7 | 1:156052655 | GATGAGAAAACTGAG[A/G]ATCAGCGAGGTAAGG | 56893 |
rs775905995 | snp | A/G | | | | | GRCh38.p7 | 1:156034171 | AAAAGATAAAACCCC[A/G]TAGGTGTGAAAAGAC | 56893 |
rs775935338 | snp | A/C | | | downstream-variant-500B | LOC105371729 | GRCh38.p7 | 1:156033225 | ACTGACTCAGCTGTG[A/C]GCTTCACTAATGGGT | 56893 |
rs775971750 | snp | C/G | | | intron-variant | LOC105371729 | GRCh38.p7 | 1:156032656 | TTTTTAACCTCTGCT[C/G]TCTGCTCAGTTCTCA | 56893 |
rs776016052 | snp | C/T | | | intron-variant | UBQLN4 | GRCh38.p7 | 1:156051009 | ATGGGGTCCCCTATC[C/T]CCATCAGACCAGGAG | 56893 |
rs776124818 | snp | C/T | 6.59055e-05 | 0.00574007 | synonymous-codon, upstream-variant-2KB | LAMTOR2, UBQLN4 | GRCh38.p7 | 1:156055347 | TGCCATAGCCAGTAA[C/T]ATCTGGGCCGCCTAC | 56893 |
rs776146402 | snp | C/T | 1.72243e-05 | 0.0029346 | intron-variant, downstream-variant-500B | UBQLN4 | GRCh38.p7 | 1:156041855 | ACCTTGCTGCCCTCC[C/T]GCCCCCCTACCCTCA | 56893 |
rs776214362 | in-del | -/G | | | intron-variant | UBQLN4 | GRCh38.p7 | 1:156051968 | CTCATCTCTAGTCAT[-/G]GGAAGTCCTTTCTGT | 56893 |
rs776241395 | snp | C/T | 1.64808e-05 | 0.00287057 | synonymous-codon, nc-transcript-variant | UBQLN4 | GRCh38.p7 | 1:156048606 | GCTCAGGGCCCGGTC[C/T]TGGTTCCGCATCATC | 56893 |
rs776331199 | snp | A/C | 8.72227e-05 | 0.00660331 | intron-variant | UBQLN4 | GRCh38.p7 | 1:156048709 | ACCAGGGGAGCACCA[A/C]CCTAGGAAAAGGGTG | 56893 |
rs776398355 | snp | A/C | 1.66535e-05 | 0.00288556 | intron-variant | UBQLN4 | GRCh38.p7 | 1:156042724 | AGAAACTGCCCCCAA[A/C]CAAGAGGAACTCTCT | 56893 |
rs776427662 | snp | A/C/T | 3.29881e-05 | 0.00406115 | intron-variant, upstream-variant-2KB | LAMTOR2, UBQLN4 | GRCh38.p7 | 1:156055446 | GAGAGGGGAGCCAGA[A/C/T]TTCCCCTGTCCCCCA | 56893 |
rs776511401 | snp | C/G/T | 3.29496e-05 | 0.00405881 | missense, nc-transcript-variant | UBQLN4 | GRCh38.p7 | 1:156037063 | TGCAGGTTAGCCTCA[C/G/T]GATTGATGAAGCCCA | 56893 |
rs776598221 | snp | A/T | 9.44956e-05 | 0.00687305 | intron-variant | UBQLN4 | GRCh38.p7 | 1:156051373 | AGTGAGCACTAGAAG[A/T]GGGAAGGTACCGTGA | 56893 |
rs776684845 | snp | A/G | 3.2993e-05 | 0.00406145 | missense, nc-transcript-variant | UBQLN4 | GRCh38.p7 | 1:156042821 | TCTGCATCATGCTGC[A/G]CATGTAGGGTGCTGA | 56893 |
rs776724407 | snp | C/T | | | intron-variant | UBQLN4 | GRCh38.p7 | 1:156042558 | AACTCATTTAATCCT[C/T]ACAACTATAGGAGGT | 56893 |
rs776812395 | snp | C/G | 1.74634e-05 | 0.0029549 | synonymous-codon, intron-variant | UBQLN4 | GRCh38.p7 | 1:156044038 | CCCAAAGGGGTTCGA[C/G]ACTGTCGGGTGCACC | 56893 |
rs776879454 | snp | G/T | 2.335e-05 | 0.00341679 | missense, intron-variant | UBQLN4 | GRCh38.p7 | 1:156044097 | CCCCACCGGACCCGG[G/T]GGCCTGGGAGGTGGG | 56893 |
rs776926560 | in-del | -/C | 1.66139e-05 | 0.00288213 | intron-variant | UBQLN4 | GRCh38.p7 | 1:156042740 | CAAGAGGAACTCTCT[-/C]CCCAACAATACTCTC | 56893 |
rs776971380 | snp | A/C | 1.70819e-05 | 0.00292244 | utr-variant-3-prime, nc-transcript-variant | UBQLN4 | GRCh38.p7 | 1:156036927 | GGATTGACAGAAGAA[A/C]CGAATGCTGACATCG | 56893 |
rs777084755 | snp | A/G | 0.000116816 | 0.00764161 | intron-variant, missense, nc-transcript-variant | UBQLN4 | GRCh38.p7 | 1:156051161 | CAGCCCCCGGAGAGG[A/G]CCCCCCACCACTGCT | 56893 |
rs777087222 | snp | C/T | 1.65844e-05 | 0.00287957 | upstream-variant-2KB, synonymous-codon, nc-transcript-variant | LAMTOR2, UBQLN4 | GRCh38.p7 | 1:156053603 | TACTACCTCCTTGAC[C/T]GAGGCTCGATCGCAG | 56893 |
rs777116059 | snp | C/T | | | missense, nc-transcript-variant | UBQLN4 | GRCh38.p7 | 1:156050419 | ACATCATATCCTGGA[C/T]CAGGGGGTTCTCCAT | 56893 |
rs777172741 | snp | G/T | 1.70731e-05 | 0.00292169 | missense, downstream-variant-500B, nc-transcript-variant | UBQLN4 | GRCh38.p7 | 1:156042197 | GGAGCTGCTCCTGCA[G/T]TTGGGGGTTCCCCGC | 56893 |
rs777204112 | snp | A/T | | | intron-variant | UBQLN4 | GRCh38.p7 | 1:156048944 | AGGCTCAGAGTGTCC[A/T]AAGAAGTGTCAGGGT | 56893 |
rs777349795 | snp | C/T | | | intron-variant | UBQLN4 | GRCh38.p7 | 1:156038457 | TTGAGGTCAGGAGTT[C/T]GAGACCAGACTGGCC | 56893 |
rs777402101 | snp | C/T | | | intron-variant | UBQLN4 | GRCh38.p7 | 1:156045395 | CACCTCACCCCACCT[C/T]GTTCTGGGCTCGCTT | 56893 |
rs777542631 | snp | A/C | 2.45709e-05 | 0.00350498 | intron-variant | UBQLN4 | GRCh38.p7 | 1:156051063 | TCTTGGCTTTCCCCA[A/C]CTCCCCAACCCCAAA | 56893 |
rs777739449 | snp | C/G | | | intron-variant | UBQLN4 | GRCh38.p7 | 1:156042631 | AGGCTAAATAACTTG[C/G]TTAACTCACACAGCT | 56893 |
rs777792126 | snp | C/T | | | intron-variant | UBQLN4 | GRCh38.p7 | 1:156047381 | CCCAAATAGCTGGGA[C/T]TACAGGCATGTGCCA | 56893 |
rs777793884 | snp | A/G | | | downstream-variant-500B | LOC105371729 | GRCh38.p7 | 1:156033144 | TGTAGCTGCTGCCAC[A/G]GGAAGCAGAAGTCAG | 56893 |
rs777861356 | snp | A/G | | | intron-variant | UBQLN4 | GRCh38.p7 | 1:156044698 | TGGCTCTCTACTTGA[A/G]CCCCGATCTTCCCTT | 56893 |
rs777903399 | snp | A/G | | | intron-variant | UBQLN4 | GRCh38.p7 | 1:156052340 | TTTATTATTATTTTT[A/G]TCTTGAGATGGAGTC | 56893 |
rs777973439 | snp | A/G | | | intron-variant | UBQLN4 | GRCh38.p7 | 1:156049797 | CTGGAACTCCCAAAG[A/G]GCAACATCACAACAG | 56893 |
rs778033832 | snp | C/T | 1.64909e-05 | 0.00287144 | missense, upstream-variant-2KB | LAMTOR2, UBQLN4 | GRCh38.p7 | 1:156055297 | TCACTGCTGGCCTAC[C/T]CTGGTTACGGGGACA | 56893 |
rs778061833 | snp | A/C | | | intron-variant | UBQLN4 | GRCh38.p7 | 1:156047709 | GATCATCCTGGCTAA[A/C]ATGGTGAAACCCCAT | 56893 |
rs778144669 | snp | C/T | 2.37099e-05 | 0.00344302 | intron-variant, upstream-variant-2KB | LAMTOR2, UBQLN4 | GRCh38.p7 | 1:156055005 | GCTGCAGTGGGGCGG[C/T]GCGCGGCTCCCTGAG | 56893 |
rs778186037 | snp | A/C | 1.84855e-05 | 0.00304013 | intron-variant | UBQLN4 | GRCh38.p7 | 1:156041443 | GAAACCTCCCAGGAT[A/C]AAAGTGGTGCTCCCA | 56893 |
rs778192309 | snp | A/G | 1.68267e-05 | 0.00290053 | intron-variant | UBQLN4 | GRCh38.p7 | 1:156048682 | AGGGAGAGAGACAAA[A/G]TGGGCCCCGGAACCA | 56893 |
rs778385866 | snp | A/G | 1.65119e-05 | 0.00287327 | intron-variant | UBQLN4 | GRCh38.p7 | 1:156042770 | CCTCATGCTGGTTTC[A/G]TACCTGAGCAGCAAA | 56893 |
rs778677043 | snp | A/G | 1.66838e-05 | 0.00288818 | intron-variant | UBQLN4 | GRCh38.p7 | 1:156037156 | CAGGCCTTGTGAAGT[A/G]GGCACAGGACCAATC | 56893 |
rs778691958 | in-del | -/TTTTTT | | | intron-variant | UBQLN4 | GRCh38.p7 | 1:156040443 | TCACAGTCCACACAT[-/TTTTTT]TTTTTTTTTTTTTTT | 56893 |
rs778763474 | snp | C/T | 1.6715e-05 | 0.00289089 | missense, nc-transcript-variant | UBQLN4 | GRCh38.p7 | 1:156048518 | GTTCCCGGGCAGCAC[C/T]GAACATGGGCTCCTG | 56893 |
rs778803302 | snp | A/G | | | intron-variant | UBQLN4 | GRCh38.p7 | 1:156041726 | AAGAAAGGGATGAGA[A/G]TGTGAGATCCAGAAG | 56893 |
rs778996041 | snp | C/G | 4.52642e-05 | 0.00475711 | upstream-variant-2KB, intron-variant | LAMTOR2, UBQLN4 | GRCh38.p7 | 1:156053578 | CGCTCCCCCCGCCCC[C/G]CGCCTGCTGTACTAC | 56893 |
rs778998806 | snp | A/G | | | intron-variant | UBQLN4 | GRCh38.p7 | 1:156043918 | CTTCAAAATCCTGGA[A/G]CAGTATGAACCCCAT | 56893 |
rs779135649 | snp | A/G | | | intron-variant | UBQLN4 | GRCh38.p7 | 1:156049950 | CTTTCCCCCTGGTTC[A/G]TCTTCCTCCTTTGGG | 56893 |
rs779168949 | snp | C/T | 1.72133e-05 | 0.00293366 | missense, nc-transcript-variant | UBQLN4 | GRCh38.p7 | 1:156050340 | CTGATCTCAGGGTTC[C/T]GCTCCATCAACTGCT | 56893 |
rs779272126 | snp | A/G | 5.0981e-05 | 0.00504855 | intron-variant | UBQLN4 | GRCh38.p7 | 1:156048691 | GACAAAATGGGCCCC[A/G]GAACCAGGGGAGCAC | 56893 |
rs779441917 | snp | C/G | 1.82814e-05 | 0.0030233 | missense, nc-transcript-variant | UBQLN4 | GRCh38.p7 | 1:156041591 | GGCGTGGCTGGTGAG[C/G]AAGTGGGGGCCTCGG | 56893 |
rs779488630 | snp | G/T | 1.64825e-05 | 0.00287071 | missense, upstream-variant-2KB | LAMTOR2, UBQLN4 | GRCh38.p7 | 1:156055318 | TACGGGGACACTGAC[G/T]CCCGGGTCACCGCTG | 56893 |
rs779532502 | in-del | -/TG | | | intron-variant | UBQLN4 | GRCh38.p7 | 1:156037306 | CAAGTCCTAAATAAC[-/TG]TGTAATGGCCGGGTA | 56893 |
rs779532617 | snp | A/G | 1.64852e-05 | 0.00287094 | synonymous-codon, upstream-variant-2KB | LAMTOR2, UBQLN4 | GRCh38.p7 | 1:156055308 | CTACTCTGGTTACGG[A/G]GACACTGACGCCCGG | 56893 |
rs779655365 | snp | A/G | | | intron-variant | UBQLN4 | GRCh38.p7 | 1:156052071 | TCTTCTCTCAGCTCC[A/G]TCCCAGAGTCTCCCA | 56893 |
rs779778334 | snp | A/G | | | intron-variant | UBQLN4 | GRCh38.p7 | 1:156045055 | TCCAGCACCTAGCAC[A/G]GAGCTCTGGCTGAGG | 56893 |
rs779898711 | snp | A/G | 2.03535e-05 | 0.00319004 | intron-variant | UBQLN4 | GRCh38.p7 | 1:156042952 | AAACAGGAGAGAAAG[A/G]GTCCAGATGGAAACC | 56893 |
rs779899722 | snp | A/G | 3.32513e-05 | 0.00407732 | synonymous-codon, nc-transcript-variant | UBQLN4 | GRCh38.p7 | 1:156041563 | GGAAGCCCCTGTTGG[A/G]GAAGATGTGGCTGGC | 56893 |
rs780042975 | snp | C/T | 4.36605e-05 | 0.00467208 | missense, intron-variant | UBQLN4 | GRCh38.p7 | 1:156044093 | CCCTCCCCACCGGAC[C/T]CGGGGGCCTGGGAGG | 56893 |
rs780052022 | in-del | -/GGA | 3.32342e-05 | 0.00407627 | cds-indel, nc-transcript-variant | UBQLN4 | GRCh38.p7 | 1:156041561 | CTGGAAGCCCCTGTT[-/GGA]GAAGATGTGGCTGGC | 56893 |
rs780122617 | snp | C/T | 2.02517e-05 | 0.00318205 | upstream-variant-2KB, synonymous-codon, nc-transcript-variant | LAMTOR2, UBQLN4 | GRCh38.p7 | 1:156053693 | CTCGGCCCCGCTCGG[C/T]TCCGCCATGCCGCCG | 56893 |
rs780136893 | snp | A/C | | | intron-variant | UBQLN4 | GRCh38.p7 | 1:156043657 | CTTTCCCCCAGCCTC[A/C]CATCTGCCTCTCCCC | 56893 |
rs780302307 | snp | A/G | 8.38174e-05 | 0.00647315 | missense, downstream-variant-500B, nc-transcript-variant | UBQLN4 | GRCh38.p7 | 1:156041969 | TGGTAAGGATGGAGA[A/G]TGACTCTGGGTTCTG | 56893 |
rs780324362 | snp | C/T | | | intron-variant | UBQLN4 | GRCh38.p7 | 1:156040225 | ATGGTGAAACCCCAT[C/T]TCTACTAACAATACA | 56893 |
rs780398598 | snp | A/G | 4.82032e-05 | 0.0049091 | synonymous-codon, nc-transcript-variant | UBQLN4 | GRCh38.p7 | 1:156041668 | TATCCCAAAGGAGCC[A/G]AGGCTGTAGGCAAGA | 56893 |
rs780456049 | snp | C/G | | | upstream-variant-2KB | LAMTOR2, UBQLN4 | GRCh38.p7 | 1:156054696 | TGCCTCGCGAGGCCA[C/G]AAAGAACTACGATTC | 56893 |
rs780595634 | snp | G/T | 1.66701e-05 | 0.002887 | missense, nc-transcript-variant | UBQLN4 | GRCh38.p7 | 1:156050365 | ACTGCTGCATCTGGG[G/T]GTTGGCCATAATCAT | 56893 |
rs780619793 | snp | A/G | 1.64806e-05 | 0.00287054 | missense, nc-transcript-variant | UBQLN4 | GRCh38.p7 | 1:156050421 | ATCATATCCTGGACC[A/G]GGGGGTTCTCCATGA | 56893 |
rs780647030 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant | UBQLN4 | GRCh38.p7 | 1:156036181 | GCTCGGGCCTGGATT[A/C]TTCTGCCTAAAAGAG | 56893 |
rs780780282 | snp | A/G | 3.94555e-05 | 0.00444142 | intron-variant | UBQLN4 | GRCh38.p7 | 1:156043947 | ATTCAGTCCTGGGAC[A/G]GAGGGGCTGCCCTGG | 56893 |
rs780836066 | snp | A/C | | | intron-variant | UBQLN4 | GRCh38.p7 | 1:156043068 | TTGTGGCATGAGTCC[A/C]AGTCTCTCCCAAGTC | 56893 |
rs780930866 | snp | A/T | | | intron-variant | UBQLN4 | GRCh38.p7 | 1:156049384 | CTGAAGATGGGGGCT[A/T]TCTTCTATGGAGCCA | 56893 |
rs780964810 | snp | C/G | 1.65002e-05 | 0.00287225 | intron-variant, upstream-variant-2KB | LAMTOR2, UBQLN4 | GRCh38.p7 | 1:156055452 | GGAGCCAGACTTCCC[C/G]TGTCCCCCAAAGGGG | 56893 |
rs781067157 | snp | A/G | 3.6511e-05 | 0.00427249 | missense, intron-variant | UBQLN4 | GRCh38.p7 | 1:156044066 | ACCTGGCTGGTCCCC[A/G]ATCCTCCGGTGCCCT | 56893 |
rs781153078 | snp | A/G | | | intron-variant, downstream-variant-500B | UBQLN4 | GRCh38.p7 | 1:156041759 | AAAGCAGTTGGAAGA[A/G]ACAGGAAAACAGACC | 56893 |
rs781263965 | snp | C/T | 1.65806e-05 | 0.00287924 | synonymous-codon, nc-transcript-variant | UBQLN4 | GRCh38.p7 | 1:156048540 | GGGCTCCTGGATGTC[C/T]GTGTACATGCGGCGG | 56893 |
rs781324941 | snp | A/C | 8.66063e-05 | 0.00657994 | missense, intron-variant | UBQLN4 | GRCh38.p7 | 1:156044196 | TGTCGGAGTTCCCGG[A/C]CAGGGAAGAGAAGGG | 56893 |
rs781332123 | snp | C/G | | | downstream-variant-500B | LOC105371729 | GRCh38.p7 | 1:156033220 | GTGAGACTGACTCAG[C/G]TGTGAGCTTCACTAA | 56893 |
rs781357116 | snp | C/G | 1.69591e-05 | 0.00291191 | intron-variant | UBQLN4 | GRCh38.p7 | 1:156037181 | CCAATCTTGGGGGCC[C/G]TATTTGAATTAAGGG | 56893 |
rs781368841 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | UBQLN4 | GRCh38.p7 | 1:156036834 | GCTAAGGGGTTGGAG[C/T]CCATGCCTCTAAAGT | 56893 |
rs781534003 | snp | C/T | 1.91705e-05 | 0.00309595 | utr-variant-5-prime, upstream-variant-2KB | LAMTOR2, UBQLN4 | GRCh38.p7 | 1:156054854 | GAGGCACCTCGGAGA[C/T]CTGGGTGCAAAAGCC | 56893 |
rs781583342 | snp | C/T | | | | | GRCh38.p7 | 1:156034444 | CTGGGATTACAGGCA[C/T]CTGCCACCGTGCCTG | 56893 |
rs781620809 | in-del | -/TTTTTGA | | | intron-variant | UBQLN4 | GRCh38.p7 | 1:156040459 | TTTTTTTTTTTTTTT[-/TTTTTGA]GATGGAGTCTCGCTC | 56893 |
rs781743834 | snp | A/G | | | upstream-variant-2KB | LAMTOR2, UBQLN4 | GRCh38.p7 | 1:156054553 | CTGCCAAGCGGACAC[A/G]TTGATTCCTTTCTCC | 56893 |
rs781752852 | snp | C/T | 3.69338e-05 | 0.00429715 | utr-variant-5-prime, upstream-variant-2KB | LAMTOR2, UBQLN4 | GRCh38.p7 | 1:156054882 | GCCCAGGGTTAGGAA[C/T]CGTAGGCATGCTGCG | 56893 |
rs781764933 | snp | A/G | | | intron-variant | UBQLN4 | GRCh38.p7 | 1:156052539 | ATGTTGGCCAGGCTG[A/G]TCTTGAACTCGTGAC | 56893 |
rs796221638 | snp | A/C | | | intron-variant | UBQLN4 | GRCh38.p7 | 1:156039940 | AGACTCCGTCTCAAA[A/C]AAAAAAAAAAAAAAA | 56893 |
rs796828661 | snp | C/T | | | intron-variant | UBQLN4 | GRCh38.p7 | 1:156049632 | TTTACTGCATGACTA[C/T]CACGCACCAGGCACT | 56893 |
rs796940330 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | UBQLN4 | GRCh38.p7 | 1:156036220 | GCTTCTGCTCCCCAC[C/T]GTTAATTCCAACTTC | 56893 |