SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs371738602 | snp | A/C | 0.000149052 | 0.00863157 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83666479 | TGGAAATATCTGAAA[A/C]AAGTAATGTACCTTG | 29979 |
rs371771211 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83688822 | GCCGAGATTGCACCA[C/T]TGCACTCCAGCCTGG | 29979 |
rs371771932 | snp | C/G | 3.29685e-05 | 0.00405995 | missense | UBQLN1 | GRCh38.p7 | 9:83677906 | GTACGGGAAGGTTGA[C/G]TACCTTCACCAGAGG | 29979 |
rs371834144 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83677128 | CCCTGACCTCAAGAC[A/G]GGTGCTTGACAATCT | 29979 |
rs371882979 | in-del | -/C | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83677570 | TCTATCTCAAAAAAA[-/C]AAAACAAAACAAAAC | 29979 |
rs371938365 | snp | A/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83665676 | ATAGGCTTACATCAT[A/T]ACAATAGATCAAGGA | 29979 |
rs371965529 | snp | C/G | 0.000153988 | 0.00877328 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83678409 | AAAACAGAAGCTACT[C/G]CTTGGCCTGAACCTT | 29979 |
rs371995651 | snp | A/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83699500 | CCTAGCTAAATTTTT[A/T]TTTTTTTGTAGACAG | 29979 |
rs372041448 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83669001 | TAAAGTTGTTTTAAT[C/T]ACATATGAAGTATTA | 29979 |
rs372082889 | snp | A/T | 9.93937e-05 | 0.0070489 | missense | UBQLN1 | GRCh38.p7 | 9:83686046 | ACAGTAAGTCCATCA[A/T]GAATTCCATGCTGAC | 29979 |
rs372141255 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83673039 | GAGTTCAAGCAGCCT[A/G]GCCAACATGGCGAAA | 29979 |
rs372160412 | snp | C/G/T | 1.70921e-05 | 0.00292331 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83669160 | TCACACTGCACAGTC[C/G/T]TTTTCAATACAATTA | 29979 |
rs372312899 | snp | C/G | | | intron-variant, downstream-variant-500B | UBQLN1 | GRCh38.p7 | 9:83667352 | TGATAGCCTATTTAT[C/G]TATCCAAAGTCTGGG | 29979 |
rs372352459 | in-del | -/ACAC | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83662274 | TATACATATACATAT[-/ACAC]ACACACACACACACA | 29979 |
rs372359355 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83670912 | TCCTCATCTGTACAA[A/G]TTTTTTCATGGCATT | 29979 |
rs372439267 | snp | A/C/G | 3.3093e-05 | 0.00406763 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83666473 | TTTAACTGGAAATAT[A/C/G]TGAAACAAGTAATGT | 29979 |
rs372548550 | snp | G/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83700237 | GTTCCAGGCAGAGAA[G/T]CAAGAGTGAACATCA | 29979 |
rs372553195 | snp | C/G | | | utr-variant-3-prime | UBQLN1 | GRCh38.p7 | 9:83660296 | TCCCTTGATTTTATT[C/G]GTCTGAATTCATTTT | 29979 |
rs372621536 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83705343 | TCTCCCAGGTTCAAG[C/T]GATGATTCTCCTGCC | 29979 |
rs372813123 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83695831 | AGAATCTGTGAAGTA[C/T]GCTAATCCAACAGTC | 29979 |
rs373018792 | snp | C/T | 3.3757e-05 | 0.00410821 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83678649 | AGGCATTGAAATACA[C/T]ATGAATTACATTAAT | 29979 |
rs373072944 | snp | A/G | 5.0109e-05 | 0.0050052 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83665178 | CTAGTGGTTACAAAG[A/G]AATTAAAATCAGTGA | 29979 |
rs373182401 | snp | C/T | 5.02584e-05 | 0.00501265 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83661965 | AAAAAAAAATTAATC[C/T]AACTCTAAAGGAAGC | 29979 |
rs373223153 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant, utr-variant-3-prime | UBQLN1 | GRCh38.p7 | 9:83667528 | GGAACATACAGTATT[C/T]ATTTCAAAGTGACCA | 29979 |
rs373350168 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83673266 | ATTTTTGGTCGGGTG[C/T]AGTGACTTACACCTG | 29979 |
rs373472586 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83676223 | ATGCTGACAATCTGA[C/T]AGGCCAGCAGAGTAA | 29979 |
rs373503602 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83670342 | CTGTTTTTAATAGTT[C/T]TTGTTTTTCCTATTT | 29979 |
rs373528219 | snp | C/T | 3.31455e-05 | 0.00407083 | missense | UBQLN1 | GRCh38.p7 | 9:83669235 | GCATCATGCTTCTCA[C/T]GTAGGGGGCAGACAA | 29979 |
rs373550475 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83676658 | TGTGATCATTAATTA[C/T]TCTTCTCATTCTGAT | 29979 |
rs373567701 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83682225 | AGGAGGCAGAGGTTG[C/T]GGTGAGCCTAGATCG | 29979 |
rs373681913 | snp | G/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83663129 | GGGAAAGGGGGAAGG[G/T]GAAGAGGAAAGGGAA | 29979 |
rs373683705 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83704184 | TGGACACTTTCAGTG[A/G]AATTTTAATGTCATT | 29979 |
rs373737788 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83696533 | AGTCCCAGTTTCTTC[A/G]GAAGCTGAAGTGGGA | 29979 |
rs373757611 | snp | C/T | 0.000109894 | 0.00741181 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83680086 | AAGTCAGAAAATTTA[C/T]CATTAACATGACATA | 29979 |
rs373806827 | snp | A/C | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83681206 | CTCTTTGGAGGACTT[A/C]AATCAAGGAGAAACC | 29979 |
rs373839563 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83686575 | AATGCATTGCTTCCC[A/G]ATATCCTTATTCTTT | 29979 |
rs373856747 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83690451 | GTGACTTCTTGGGAG[C/T]TGGTATCATGTTCTA | 29979 |
rs374076954 | in-del | -/A | 0.00835141 | 0.0640778 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83677598 | AACAAAAGCAACATG[-/A]AAAATATAGTTTATA | 29979 |
rs374105880 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83673952 | TACTACAGCTGCACA[C/T]CATGCCCGGTTACTT | 29979 |
rs374175731 | snp | C/T | 3.33028e-05 | 0.00408048 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83664060 | TACAGAAAGCACAAA[C/T]AGGAAATATCCTAAG | 29979 |
rs374176575 | snp | A/G | 1.64868e-05 | 0.00287109 | missense | UBQLN1 | GRCh38.p7 | 9:83682978 | GGTTGCTAGTAGCAG[A/G]ACCAGATGTAGAGTT | 29979 |
rs374182108 | snp | C/G | 0.000131817 | 0.00811735 | missense | UBQLN1 | GRCh38.p7 | 9:83663997 | TAGATCCATTAGTTC[C/G]CGAAGAGCCTCCAGT | 29979 |
rs374183232 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83684121 | TGGCCCTTGAAATTC[C/T]TGAAAACAATAAAAA | 29979 |
rs374239052 | in-del | -/AG | | | intron-variant, utr-variant-3-prime | UBQLN1 | GRCh38.p7 | 9:83667782 | GTTTTTACACTCAAG[-/AG]TCTTTTTAAATATTT | 29979 |
rs374356815 | snp | C/T | 0.000153988 | 0.00877328 | missense | UBQLN1 | GRCh38.p7 | 9:83677894 | TCTCTATTTTCTGTA[C/T]GGGAAGGTTGACTAC | 29979 |
rs374444040 | snp | A/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83684846 | AAGGAAATAAAAAAA[A/T]CCCTTCCAGATGATA | 29979 |
rs374452865 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83702308 | ATTACACTTCAATTA[C/T]GCTCTTTCTTAAAAA | 29979 |
rs374602052 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83678843 | CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGACTAC | 29979 |
rs374629577 | in-del | -/AT | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83682290 | ACTCTGTCTCAAAAA[-/AT]ATATATATATATATT | 29979 |
rs374684964 | snp | C/T | 1.66261e-05 | 0.00288319 | synonymous-codon | UBQLN1 | GRCh38.p7 | 9:83677947 | CACCAAGGAAGCAAA[C/T]GGATTACCACCAAAC | 29979 |
rs374835504 | snp | A/C | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83695151 | GGACAGAATCACCCA[A/C]AAAAAAAAAAAAGTT | 29979 |
rs374874794 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83699297 | TGACTTCAGTCCTTC[C/T]TTTTGATTAAAGTGG | 29979 |
rs374881278 | snp | C/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83692825 | CCATTGCACTCCAGC[C/G]TGGGCAACAAGAGCG | 29979 |
rs374988467 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83671737 | TAATTTTTAAGGCCC[C/T]AGGATTACTGGAATA | 29979 |
rs375072238 | snp | C/T | 1.65441e-05 | 0.00287607 | synonymous-codon | UBQLN1 | GRCh38.p7 | 9:83678450 | GATCACCTGCTCTTG[C/T]GCAGCACTCAGCATT | 29979 |
rs375101475 | in-del | -/AACAAAA | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83666123 | GTCCTCAAAAGCAAA[-/AACAAAA]TGTTCTTTCCTCAGA | 29979 |
rs375123417 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83662610 | ATAATTTGGAGGCTT[A/G]TAAGTTAACTTATGT | 29979 |
rs375124390 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83695124 | TATATATGAACATAT[A/G]AATACCTTTCTGGAC | 29979 |
rs375151109 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83665840 | TCAAGTACTCGTTTA[C/T]ACTATAACCTTCCTT | 29979 |
rs375385332 | snp | G/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83674803 | ACCGGAAAATTACCC[G/T]CTATAAATAGTCTGA | 29979 |
rs375392282 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83699423 | CATAGCTCAGTGTAA[A/C]CTCCAAACTCCTGGG | 29979 |
rs375548748 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83665544 | TTATCTGTTACTAAT[A/G]TAACAATTTTACCAG | 29979 |
rs375559347 | snp | G/T | 0.000153988 | 0.00877328 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83677708 | ACAAAGAAAAAAGCC[G/T]GAGTTGTTAAAAGCA | 29979 |
rs375581131 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83700494 | TCACAGCCCCTCTCT[A/G]AAGAGAAGGAATCAC | 29979 |
rs375582280 | snp | A/G | 3.37992e-05 | 0.00411077 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83685957 | TACTTTTAGAAGTAC[A/G]AACATTTATCCACAA | 29979 |
rs375591184 | snp | A/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83691235 | CTTGGGCAGGTCAAC[A/T]GAAAGGAAATGGAAT | 29979 |
rs375596467 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83666898 | TCTAGATCTGAAAAG[A/G]ACCACTACATCTACC | 29979 |
rs375631819 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83689974 | GGTTCAGTTTAAGAC[C/T]GTTAAAGAGCGTTAC | 29979 |
rs375661841 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | UBQLN1 | GRCh38.p7 | 9:83661134 | CAAACCTGACTAACC[A/G]GCACTTTTGCTGGGA | 29979 |
rs375755625 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83705765 | AGTGGAAAACTACAC[A/G]CTAATAAAAAGAAAG | 29979 |
rs375783979 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83666292 | AGGAAAAATGTTTAT[C/T]ATCAAATTTTTTCAA | 29979 |
rs375792947 | snp | C/T | 0.000593286 | 0.0172131 | utr-variant-3-prime | UBQLN1 | GRCh38.p7 | 9:83661742 | TTAAAGTTTAAGAGC[C/T]GTTATCAAAAATAAA | 29979 |
rs375989972 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83672023 | TGTACCTTTACATTA[C/T]GGAGTTGGCTTCTTT | 29979 |
rs376002949 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83673931 | CCTCAGCCTCCCAAG[C/T]AGCTGTACTACAGCT | 29979 |
rs376149795 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83684765 | CAGTGAGCTGAGATC[A/G]CACCGTTGCACTCCA | 29979 |
rs376171919 | in-del | -/ATAAGAG | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83684866 | TCCAGATGATACCAG[-/ATAAGAG]TTTTGAATGCCACTC | 29979 |
rs376187568 | snp | C/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83673307 | ACTTTGGGAGGCCAA[C/G]GCAGACAGATCACCC | 29979 |
rs376265428 | snp | G/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83705149 | TCAAAATGTTAGCAG[G/T]GATATGGAGCAACAG | 29979 |
rs376439766 | snp | C/T | 1.71959e-05 | 0.00293217 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83669150 | TTATTTTAATTCACA[C/T]TGCACAGTCTTTTTC | 29979 |
rs376511962 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83707212 | GGGAGGCGACGGAGG[A/G]CGGGGAACTGGGGGA | 29979 |
rs376521304 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83672488 | ACCCAATTTCAATGT[C/T]GTGTCTCAGAGAATA | 29979 |
rs376534632 | snp | C/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83683704 | AATGACCAGTTACAC[C/G]CACAAAGCTTGACTA | 29979 |
rs376599312 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83676823 | TTCTTCCTACTTATA[C/T]GCCAAGTATTAGGAC | 29979 |
rs376675955 | in-del | -/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83670382 | TAAATTTTAACTTAG[-/T]TTTTTTTTTCACATC | 29979 |
rs376694999 | in-del | -/GTCT | | | upstream-variant-2KB, intron-variant | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83709491 | CCCTTGCCTTCACCT[-/GTCT]AACTTCTACTCATCC | 29979 |
rs376904576 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83685342 | AAATATGGACACTGA[C/T]AACTAAGTCTTCGTA | 29979 |
rs376930157 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83702061 | TGAAAGCCAATCACA[A/G]AAGACCACATGATTC | 29979 |
rs376934483 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83694906 | CTCCTTACCCATCAT[C/T]AGATTTCTCCAATTC | 29979 |
rs376944218 | in-del | -/A/AA | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83685615 | ATGACTCTGTCTCTT[-/A/AA]AAAAAAAAAAAAAAA | 29979 |
rs376978764 | snp | C/T | 5.17201e-05 | 0.00508502 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83669138 | TACAAGATTAGGTTA[C/T]TTTAATTCACACTGC | 29979 |
rs376988711 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83690594 | GCAGCAGGGGCTGGG[C/T]GTGGTGGTTCATGAC | 29979 |
rs377152325 | snp | A/G | 1.67837e-05 | 0.00289682 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83685978 | TTATCCACAATTTTA[A/G]AGCTGTACATCTTCC | 29979 |
rs377173188 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83684671 | ACAAAATTAGCCGGG[C/T]GTGGTGGCGCATGCC | 29979 |
rs377175038 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83670099 | AATTCCATATGTGAT[A/G]ACAACTGTATATTTA | 29979 |
rs377209807 | in-del | -/CTGT | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83686971 | TGGTCCCAAGTCTGT[-/CTGT]TTAAAAAAAAAAAAA | 29979 |
rs377229309 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83695238 | AAGTCTCACTCTGTC[A/G]CCCAGGCTGGAGTAC | 29979 |
rs377286932 | snp | C/G/T | 0.000296738 | 0.0121772 | synonymous-codon | UBQLN1 | GRCh38.p7 | 9:83665062 | GGCTTCCGTTGCTAA[C/G/T]GTCTGTAAACCCTGC | 29979 |
rs377309746 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83688182 | CATCAGGTATATAGG[C/T]AGTAGTCAATAAATG | 29979 |
rs377346830 | snp | A/C | 0.000151593 | 0.0087048 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83685970 | ACGAACATTTATCCA[A/C]AATTTTAAAGCTGTA | 29979 |
rs377431987 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83680330 | TGAGTTACTAAAACT[C/T]TGGAATTTTCTGAGT | 29979 |
rs377434862 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83664341 | AGAGGATTGCTTTAG[C/T]CCAGGAGGTAGAGGC | 29979 |
rs377452429 | snp | C/T | 6.6011e-05 | 0.00574466 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83678603 | AAGTTCCAACGTCTA[C/T]GAAAAATATTTCCAA | 29979 |
rs377477362 | snp | C/T | 1.65562e-05 | 0.00287712 | missense | UBQLN1 | GRCh38.p7 | 9:83669253 | AGGGGGCAGACAACA[C/T]GTTTTGCATCAGTTG | 29979 |
rs377538482 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83681576 | ACGTGAAGAAGGTTA[A/G]GAGGGGGACTGAATA | 29979 |
rs377551313 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83665749 | CATAATACATGAGGC[C/T]CTAGAACTACCAGTT | 29979 |
rs377581389 | snp | A/C | 0.000562197 | 0.0167566 | synonymous-codon | UBQLN1 | GRCh38.p7 | 9:83677755 | CACCAAATTTGGCGC[A/C]GTAGTACTCTGCCCA | 29979 |
rs377610770 | snp | C/G/T | 3.35561e-05 | 0.00409599 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83683099 | TCACAGAGTAAGCAG[C/G/T]AGAGCTGATTATTTT | 29979 |
rs377637816 | snp | G/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83697481 | TGTGTGAACCCAGGG[G/T]GCGGAGGTTGCAGTG | 29979 |
rs377650691 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | UBQLN1 | GRCh38.p7 | 9:83660767 | AACAATTGGCTCACA[A/G]CTCATTTTAAATTTG | 29979 |
rs377763890 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83666797 | TTTCTACTACACTGG[C/T]AGAATAAACATAAAC | 29979 |
rs386415304 | in-del | -/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83675931 | CTAAATATTACCAAT[-/T]TTTTTTATTTTTTCA | 29979 |
rs386415305 | in-del | -/TT | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83678024 | ATAAGATATGAAACT[-/TT]TTTTTTTTTTTTTTT | 29979 |
rs386415306 | in-del | -/A | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83698913 | GTGAGACCTGTCTCA[-/A]AAAAAAAAAAAAAAA | 29979 |
rs386735693 | multinucleotide-polymorphism | CA/TG | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83697408 | ATACAAAAAATTAGC[CA/TG]GGTGTGGTGGTGTGC | 29979 |
rs386735694 | in-del | C/GGG | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83704585 | TAATCCTAGCACTTT[C/GGG]AAGCCGAGGCAGGCG | 29979 |
rs386735695 | multinucleotide-polymorphism | ACC/CCT | | | upstream-variant-2KB, intron-variant | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83708699 | CTGTATTGACAGTGG[ACC/CCT]CTGCTGCTACGATGA | 29979 |
rs397704652 | in-del | -/T | 0 | 0 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83704521 | AAAGACTTTAATTTT[-/T]ATCTATTAACAATTC | 29979 |
rs397746500 | in-del | -/A | 0 | 0 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83690756 | TCTCAAAAAAAAAAA[-/A]CAAGAACAGAAACAT | 29979 |
rs397770663 | in-del | -/A | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83703534 | AAATCCAAAAAAAAA[-/A]GAAAATCCAAAGTCC | 29979 |
rs397803965 | in-del | -/A | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83703174 | ACCAAAAAAAAAAAA[-/A]TCTCATACACAGGGA | 29979 |
rs397894216 | in-del | -/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83688393 | CAGATTAACTATTTT[-/T]CATATGCAAAATGAG | 29979 |
rs397894807 | in-del | -/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83697753 | TTTTTTTTTTTTTTT[-/T]GAGACGAAGTCTCAC | 29979 |
rs397953179 | in-del | -/AAAA | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83704846 | AAAAAAAAAAAAAAA[-/AAAA]TCTCACTTTGGTTAC | 29979 |
rs397953898 | in-del | -/A/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83682836 | ATGTTTTTTTTTTTT[-/A/T]AATTTTTGTTGTTAA | 29979 |
rs398011238 | in-del | -/A | 0 | 0 | intron-variant, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83706133 | AATTACGTCAAAAAA[-/A]CGTAAAAAATGAAGT | 29979 |
rs398087395 | in-del | -/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83697261 | TTTTTTTTTTTTTTT[-/T]TAAGACATAGGCCAG | 29979 |
rs527313265 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83684999 | CAACTACATGCCTGC[A/C]CATGTAGTCTACATG | 29979 |
rs527355325 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83688095 | CCTTTAGTACCTATC[C/T]GAAATAGTAATATAA | 29979 |
rs527440076 | snp | C/G | 0.0023933 | 0.0345097 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83708031 | TGGCGGCGTCGCCGA[C/G]TCATCCCCGGCTGGC | 29979 |
rs527443757 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83701590 | CAGCAAAAATAATAA[C/T]GAAAATAAAAAGCAA | 29979 |
rs527549791 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83668681 | TAAGGGACCTGTATA[C/T]GATTTTCAGCAGGGG | 29979 |
rs527591172 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83669059 | AAAAATTGGAGACAC[A/C]GTTTACTTATTTTTC | 29979 |
rs527695071 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83689863 | AAAATGGCCAAGAAA[C/T]TGAAACAGGAATTTC | 29979 |
rs527702930 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83682544 | AAAGCAGTTTTAGGC[A/G]AGGCTGGCTTCCCAG | 29979 |
rs527829484 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83696831 | ACTCGGGGGCAGGGG[A/G]GCTGGGTGAAGGAGA | 29979 |
rs527866512 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83677338 | GAGGCCAAGGCAGGC[A/G]GATCACCTGAGGTCA | 29979 |
rs527920802 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83708571 | AACGAACAGAAAATG[C/G]AGTGAACGCCCGTGA | 29979 |
rs527922381 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83662349 | ATTTGTGTAGCTACT[C/G]ACCAATTGAGTAACT | 29979 |
rs527960967 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83683151 | GGCACAGTGGCTCAC[A/G]CCTGTAATCCCAGCA | 29979 |
rs528001418 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83665504 | TGGATATGGTAAAAA[A/G]CCACATATTCCACCT | 29979 |
rs528099762 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83685251 | ACAAAATCCTGGAGA[A/T]AATACTGGAGAGCTC | 29979 |
rs528106831 | snp | C/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83670129 | AGGCAAATTTTCTTT[C/G]AAAACTAAGTTAATT | 29979 |
rs528209532 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83672558 | CAGTCAGTTGAACAG[C/T]CAGAACACATACATT | 29979 |
rs528220493 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83699273 | TGTGAGTCACCACTA[C/T]TGAAAAATTGACTTC | 29979 |
rs528256391 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83679645 | CGCTTTGTTGAGTTT[C/T]CTTAAACCAAGATAA | 29979 |
rs528271915 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83672733 | ACAGAGACATGAAGT[A/G]GGCACATGCTGTTGG | 29979 |
rs528429817 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83679016 | GTGAGCCACCGCGCC[C/T]GGCCAGGAGGCCACT | 29979 |
rs528443156 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83706281 | AATACCGTAAAATGC[G/T]AATTGTAGATGATGG | 29979 |
rs528505241 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83699968 | CTTGAAATCTGCCAC[A/G]GTGAGAATATTTACA | 29979 |
rs528536464 | snp | G/T | 1.64887e-05 | 0.00287125 | missense, intron-variant | UBQLN1 | GRCh38.p7 | 9:83666359 | ACTCACTTGTTGGAG[G/T]AAAGTTGGGAGCTGT | 29979 |
rs528560923 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83703491 | GTGCCATCCCCAAGA[G/T]ATCTCATTATGTATA | 29979 |
rs528561105 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83675911 | GATACAAGGAAAATA[C/T]TGTAACTAAATATTA | 29979 |
rs528572669 | snp | C/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83700839 | AACCGTATTACACAG[C/G]GCCTCGCTACTCCAT | 29979 |
rs528668774 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83687379 | TTACCAGACTGTCCA[A/T]ATAGGAAAGCTTCAG | 29979 |
rs528687427 | in-del | -/AT | 0.00119737 | 0.0244387 | downstream-variant-500B | UBQLN1 | GRCh38.p7 | 9:83659704 | ACCACCACATGTATA[-/AT]AAAGAAACCATGACG | 29979 |
rs528764045 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83700727 | GAAGTCCTCAGGCAG[G/T]AAAAAAAGTATTAAC | 29979 |
rs528925756 | snp | A/G | 3.31087e-05 | 0.00406857 | synonymous-codon | UBQLN1 | GRCh38.p7 | 9:83669254 | GGGGGCAGACAACAT[A/G]TTTTGCATCAGTTGT | 29979 |
rs528964435 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83669889 | ATCAGGAGCCTGATT[A/G]CGTGGGTTCAAATCT | 29979 |
rs529060624 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83690633 | CAGCACTTTGGGAGG[C/T]CAACATGGGAGGACT | 29979 |
rs529131584 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83697134 | CAAGGCAGTTTGGGG[C/T]AGTGGATCGGTGAGG | 29979 |
rs529164665 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83703335 | GGAAAAATCCCATAT[A/G]TAACACCTTTGCTTT | 29979 |
rs529191605 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83697659 | CTCGCAGATTCAAGA[A/G]ATTCTTCCACCTCAG | 29979 |
rs529272054 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83678116 | AAGCTCCGCCTCCTG[G/T]GTTCACACCATTCTC | 29979 |
rs529336849 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83683739 | AAAAACTTTTTTATC[A/T]TGGCCAGGTGCGGTG | 29979 |
rs529411527 | snp | A/G | 0.0287284 | 0.116357 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83677519 | GTGAGCTGAGATCGT[A/G]CCATTGTACTCCAGC | 29979 |
rs529430920 | snp | C/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83678803 | TTCACTGCAAGCTCC[C/G]CCTCCCGGGTTCACA | 29979 |
rs529491205 | snp | G/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83662243 | ACATGCAGAAAAACC[G/T]GTATGTGTGTGTGTA | 29979 |
rs529505722 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83665319 | CTCTTTGACAGCAAA[C/T]CTAGTGTGCAAATTA | 29979 |
rs529512769 | snp | C/G | 0.0158469 | 0.0875917 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83704587 | ATCCTAGCACTTTGG[C/G]AAGCCGAGGCAGGCG | 29979 |
rs529564841 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83683718 | CCCACAAAGCTTGAC[C/T]ATATAAAAAACTTTT | 29979 |
rs529571828 | in-del | -/AAG | 0.00119737 | 0.0244387 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83687528 | AAGGAAATTGCTGCC[-/AAG]AAGGTGTTTTGGAAA | 29979 |
rs529583147 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83671319 | TGACATTGAGAATGG[G/T]GAATGAATCCTTTCC | 29979 |
rs529598121 | in-del | -/A | 0.30191 | 0.244551 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83675469 | CTTCCTATGCCGTCA[-/A]AAAAAAAAAAAAAAT | 29979 |
rs529601906 | snp | G/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83698384 | CTACTTCAAACTGAG[G/T]TATGCTTAAGTGTAA | 29979 |
rs529622729 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83671841 | GAAGCTAAGAATTCA[C/T]TTCTCTCCAGAAATG | 29979 |
rs529629681 | in-del | -/C | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83681938 | CTATATGGATGGGCA[-/C]CTTACAAACCGGTAA | 29979 |
rs529642321 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83680981 | GGTATTGGACAATTG[A/G]CTGGTGTCAGAAAAA | 29979 |
rs529699068 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83673536 | GGTGACAGGTCGAGA[C/G]TCGGTCTTTTAAAAA | 29979 |
rs529757372 | snp | A/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83689294 | TTGTATGAATATACC[A/T]CCTATTTTGCTTATC | 29979 |
rs529865892 | snp | A/G | 0.000154536 | 0.00878885 | synonymous-codon, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83707527 | GCTATTCTCGGGCAC[A/G]GCGAATTCCTCCTTT | 29979 |
rs529897779 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | UBQLN1 | GRCh38.p7 | 9:83660959 | GTCCTAGGCAAATGC[A/G]CTTTGGGGTATACTA | 29979 |
rs530109530 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83688233 | TCTCTTAATACTCAA[C/T]AATTTTTCGAGGAAG | 29979 |
rs530115678 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83701496 | TATGGGGACTCCCCA[A/T]ACCACAGTGAGAACT | 29979 |
rs530215455 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83675743 | ATTAAAATCAAATGC[G/T]TTTGGAATGAGTACG | 29979 |
rs530372923 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83682515 | AACAAACAAAAACTA[A/G]TATAAGAAAAACAAA | 29979 |
rs530384599 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83688798 | CCTGGGAGGCAGAGG[G/T]TGCAGTGAGCCGAGA | 29979 |
rs530520099 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83698658 | TGGCTCACACTTGTA[C/T]AATCCTAGCATTTTG | 29979 |
rs530564407 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83675564 | AACATTTTTCAGACC[C/T]CAATGCAAATGCAAA | 29979 |
rs530597158 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83704020 | ACATAGAAATACTTA[C/T]TGAAAGAAATTTTAA | 29979 |
rs530662138 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83698203 | GTTCAAAAAGGGGAA[A/G]AAAGAGCCAGTGATA | 29979 |
rs530681155 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83684484 | TCAGGTGTGAGCCAC[C/G]GCGCCTGGCCTGATT | 29979 |
rs530781830 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83673133 | TACTGGGGAGGCTGA[A/G]AAGGGAGAATCGTTT | 29979 |
rs530797831 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83691988 | CCTAATTTAGATACT[A/G]GAACCACTTCCAAGT | 29979 |
rs530839847 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83670485 | TTTTGGTTTCCCAGC[A/G]CATACAAAAGTTGTT | 29979 |
rs530860692 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83685204 | TTGGTAAACAACAGC[A/G]TAAAAACTTACAGGA | 29979 |
rs530863617 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83680978 | GCTGGTATTGGACAA[C/T]TGGCTGGTGTCAGAA | 29979 |
rs530887360 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83679001 | GCTGGGATTACAAGC[A/G]TGAGCCACCGCGCCC | 29979 |
rs530923492 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83672539 | GAGAGACAAGTGGAA[C/G]AGCCAGTCAGTTGAA | 29979 |
rs531014559 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83693940 | AATTAAGAGACATAC[A/C/G]GAAATTTCCTGGGCA | 29979 |
rs531090304 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83699372 | TAAGAGACCAAGTCT[C/T]ATTCTGTCACCACAG | 29979 |
rs531131473 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime | UBQLN1 | GRCh38.p7 | 9:83660040 | GACACTATCCCACAC[C/T]GAATACCACCATTTG | 29979 |
rs531186335 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83669105 | TCATACACAACACAA[A/G]TGTGCCAAAATCACA | 29979 |
rs531257447 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83682460 | CTCTAGCCTCCGTGA[C/T]TGAGCAAGATCCTGC | 29979 |
rs531257554 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83674848 | GTAAGACCATTTTTT[A/T]AAAAGTTGAGAAATA | 29979 |
rs531406042 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83696953 | TTAAATAAACTTCTT[A/T]AAAAAAGATACAGAG | 29979 |
rs531470745 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83662646 | TTAATTCTAATACTC[C/T]AAATCCTTCTTTCTT | 29979 |
rs531478421 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83702190 | GCTAAAGGGTACAGC[A/G]TTTCTTTTTGAGGGT | 29979 |
rs531541050 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83696346 | ATAATGCCATCAGAC[A/G]CTTAAGTTGACTAAG | 29979 |
rs531634876 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83662949 | GGTGTGGTGGTCTGC[A/G]CCTGTAATCCCAGCT | 29979 |
rs531638114 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83677455 | TAATCCCAGCTACTC[A/G]GGAGGCTGAGGCAGA | 29979 |
rs531675785 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83689964 | TGCACTGAATGGTTC[A/C]GTTTAAGACTGTTAA | 29979 |
rs531723591 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83676835 | ATACGCCAAGTATTA[C/G]GACTAAAATTGTCAC | 29979 |
rs531738408 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83683181 | ACTTTGGGAGGCCGA[A/G]GCTGGCTGATCACGA | 29979 |
rs531858929 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83690413 | TGCCCAAAGTGAGAA[C/T]AGTGGTTACCTTAAG | 29979 |
rs531900636 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83664285 | TTAGCTGGGTGTGCT[A/G/T]GTGCACACCTGTAGT | 29979 |
rs531926030 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83686522 | GGTCCTACTATAGGT[A/G]CACATATCCTATATT | 29979 |
rs531950183 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83709829 | AAATCAGAGATTAGT[A/G]AACTTTCTGGGAGGG | 29979 |
rs531954712 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83703637 | ACAGCACCTTGGAAT[A/G]TACACAGTGCAGTTT | 29979 |
rs531990747 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83681852 | GCTGTCTCTTCTGCC[A/G]TGTTCCAAATGGTAG | 29979 |
rs531996152 | snp | A/G | | | utr-variant-3-prime | UBQLN1 | GRCh38.p7 | 9:83661414 | ACCACAAATTATAGA[A/G]TGCAAATGATTTGCT | 29979 |
rs532046560 | in-del | -/TTATT | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83691944 | TTCATAATTCAGTTC[-/TTATT]TTAAATTTCAAACCA | 29979 |
rs532155393 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83686690 | CAGTCCTGTTCCTTT[A/C]TTTCTAGTTGAATAC | 29979 |
rs532155703 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83693837 | TTTTGCTACATACTA[A/G]TTGTGTGACCTGGAG | 29979 |
rs532159247 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83679139 | TATGAAAGGGGCCAG[C/T]TTCCCCCCCAAAACC | 29979 |
rs532185634 | snp | A/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83669997 | CAGTATCTACTTCAT[A/T]GGGTGGTTGTAAGAA | 29979 |
rs532221394 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83693153 | TCTCAACAACCATAA[C/G]AATCAAAATTCTAAT | 29979 |
rs532247989 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83693603 | ATCAAATAAGAGTAC[A/G]CAGAGAATGTGAAAT | 29979 |
rs532294323 | snp | G/T | 7.21475e-05 | 0.00600571 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83686161 | CTTCCTTAAACTAAA[G/T]AAAAATAAAATAAGT | 29979 |
rs532361335 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83706395 | CTGGGAGACAAAAAC[A/T]AAAGTGATAATTCTG | 29979 |
rs532399772 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83679689 | TAGCTTAACCATACA[C/T]ACAGGACAATCTCAT | 29979 |
rs532471450 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | UBQLN1 | GRCh38.p7 | 9:83660771 | ATTGGCTCACAACTC[A/G]TTTTAAATTTGTGTA | 29979 |
rs532477388 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83673453 | AGGAGGCTGAGGCAC[A/G]AGAATCTCTAGAACC | 29979 |
rs532581281 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83681924 | GAGTCTCTGAGGGAC[C/T]ATATGGATGGGCACC | 29979 |
rs532692950 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83700794 | GCAAGCAAAGAAAGA[A/C]GGCATCTGCAAAAAA | 29979 |
rs532742225 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83688146 | TTGTAAGAATTAAAC[G/T]AGAATGTATATAAAT | 29979 |
rs532813622 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83697715 | CATGCACCACCACAC[G/T]CGGCTATTTTTTGTA | 29979 |
rs532918205 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83703578 | TCCCAAGCATTTCCC[A/G]TAAGGGATACTCAAA | 29979 |
rs532969549 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83684353 | GTGCACACCACTGTG[C/T]TGGGCAATTTTTTGT | 29979 |
rs533015813 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83673494 | AGGTTGCAGTGAGCC[A/G]TGATCATGCTACTGC | 29979 |
rs533062315 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83690745 | AACCAGACTCTGTCT[A/C]AAAAAAAAAAACAAG | 29979 |
rs533181363 | in-del | -/AGTTGTGCCTGGAGAGTGGTGACCTGGGGGGAGCAGTCAAC | 0.00119737 | 0.0244387 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83700265 | CATGAAGCAGTCAAG[lengthTooLong]AGTTGTGCCTGGAGA | 29979 |
rs533207282 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83678147 | CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGACTAC | 29979 |
rs533241925 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83698148 | ATGCCTGCAATAAAT[A/G]TTGGCCATTATGTCA | 29979 |
rs533292611 | snp | C/G | 4.96652e-05 | 0.00498298 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83678616 | TACGAAAAATATTTC[C/G]AAAAAAAGAAAAAAA | 29979 |
rs533306590 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83691329 | ATAATCACCAAAGGC[C/T]AAAAGATGATCCATT | 29979 |
rs533340185 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83671920 | CATTAAAAACTGGTT[A/G]TTTCATGTGGCCACG | 29979 |
rs533401605 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83681402 | GAACTCAATCTAGTA[A/G]GAAAGACAGACAAGA | 29979 |
rs533419273 | snp | G/T | | | utr-variant-3-prime | UBQLN1 | GRCh38.p7 | 9:83660575 | CTGAATGATACTTCT[G/T]TACTACACTATATGC | 29979 |
rs533463120 | snp | A/C | 0.0788843 | 0.182262 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83666126 | CTCAAAAGCAAAAAC[A/C]AAATGTTCTTTCCTC | 29979 |
rs533493933 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83695551 | ATTTTAAAGCAAAAA[-/T]ATGTAAAAGGTATTT | 29979 |
rs533579784 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83707088 | CCCACCCCTTTTTAA[C/T]TCATGAAACAAAACC | 29979 |
rs533597185 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83699325 | TGGCTAATAGGAAAA[C/T]TACATATGTGGCTCA | 29979 |
rs533606860 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83673562 | AAAAAAAAAAAAAAA[A/C]AAAAACAAAAAAAAA | 29979 |
rs533643533 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83665446 | ACAGAAGATAAAGTA[C/T]TACTTCTAAGACACA | 29979 |
rs533709272 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83694937 | TAAGGTTCATGCTCT[C/G]CTTTCTCAAAATATT | 29979 |
rs533749512 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, utr-variant-3-prime | UBQLN1 | GRCh38.p7 | 9:83667999 | CTACGCATGTGCTTG[C/T]TAAAGTCAAATTTTA | 29979 |
rs533749865 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | UBQLN1 | GRCh38.p7 | 9:83660329 | GTTACTTTAACATTT[G/T]AATTTCCTGTAACTG | 29979 |
rs533752273 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83682395 | ACACCAGCAGGACAC[C/T]GTAAGCCAGGAGTTT | 29979 |
rs533773755 | snp | C/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83675234 | TTAGCTCATGCCAAA[C/G]ATTAAAATTTTAGTA | 29979 |
rs533802078 | in-del | -/TT | 0.489318 | 0.0722982 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83697734 | CTATTTTTTGTACCC[-/TT]TTTTTTTTTTTTTTT | 29979 |
rs533819415 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83707167 | CCCGGAGGCTGGCGG[C/T]GGGTCCCTTTCCTTT | 29979 |
rs533821635 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83700344 | TGGGAGCTACCAGAT[C/T]ATGTACATACTACAC | 29979 |
rs533844378 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83700985 | GGCAACTGACCAGTA[A/G]GCTACTGCAGTTTCT | 29979 |
rs533877199 | snp | A/G | | | intron-variant, downstream-variant-500B | UBQLN1 | GRCh38.p7 | 9:83667029 | GGCCTAGCACCAACA[A/G]TCCTCTGGGAAAAGT | 29979 |
rs533955052 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83675131 | CTTCATGAATTTTTA[G/T]TAACAATAACTCAAT | 29979 |
rs533974372 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83698944 | GTAAATTCTGACACA[C/T]GCTACAACATAAATG | 29979 |
rs534001014 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83687794 | CTGATTTTTAAAAAA[C/T]CTGTTTTACCTTTGT | 29979 |
rs534047244 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | UBQLN1 | GRCh38.p7 | 9:83661133 | ACAAACCTGACTAAC[C/T]GGCACTTTTGCTGGG | 29979 |
rs534181555 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83668904 | AGAGTGGGCATTCCA[A/G]AACTCTGTACTTGTC | 29979 |
rs534272208 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83688479 | TTTTTGATATCCCTC[A/G]TTATTCTGAAATAAG | 29979 |
rs534277642 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83681443 | CTATACAGATGCTAA[C/G]TACTTCAGTAAAGAA | 29979 |
rs534279397 | snp | A/C | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83687774 | ACAACAGCCAATATA[A/C]ACAACTGATTTTTAA | 29979 |
rs534362233 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83708211 | CAGTTTCCAGTTAAG[C/T]GCTGTAACGGCGCAC | 29979 |
rs534570373 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83678751 | AGACGGAGTCTTGCT[C/T]TGTCGCCCAGGCTGG | 29979 |
rs534640908 | snp | C/G/T | 0.000494988 | 0.0157243 | synonymous-codon | UBQLN1 | GRCh38.p7 | 9:83665044 | CCCTGGGATGAGGCC[C/G/T]GGGGCTTCCGTTGCT | 29979 |
rs534689185 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83691377 | AGACAATTAAAACCT[C/G]ATATCCAAAACAGCT | 29979 |
rs534755174 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83684505 | TGGCCTGATTATTAC[C/T]TAGTATTATCTCTAA | 29979 |
rs534770519 | in-del | -/T/TT | 0.4983 | 0.0291038 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83678023 | AATAAGATATGAAAC[-/T/TT]TTTTTTTTTTTTTTT | 29979 |
rs534779983 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83690384 | TTTTTAAGGGTTGGG[A/G]ACAAAATCCATGGTG | 29979 |
rs534803636 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83705480 | GTCTCGAACCTCAGG[C/G]AATCCACCCGCCTCG | 29979 |
rs534855462 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83704881 | GAGTAAAATAAAAGC[A/G]TTCACAGAATTTATA | 29979 |
rs534874366 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83671678 | TTTTTTTCTTTTTTT[C/T]TTTTTTTTCCTGTTT | 29979 |
rs534913753 | snp | C/T | | | intron-variant, utr-variant-3-prime | UBQLN1 | GRCh38.p7 | 9:83668462 | TCAAGCCCTGTGGTA[C/T]GGAACCTAGATAGTA | 29979 |
rs534977939 | snp | C/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83695420 | GGCCAGGCTGGTCTT[C/G]AACTCCTGACCTTGT | 29979 |
rs535030397 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83686770 | AATGCAAATACCCCA[A/G]ATATGAAATGCACCA | 29979 |
rs535040703 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83695941 | TTCACTTCACTTTTC[A/G]AATTAATTTTTTTTT | 29979 |
rs535100847 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83696437 | CAACATGGCAAAATC[C/T]TGTCTCTATAAAAAC | 29979 |
rs535117002 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83698980 | TGTGGACGTTATACT[A/G]AGGGAAATAAGTTAA | 29979 |
rs535171413 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83662082 | ACCTCTTGAAACTTA[C/T]CCAACATATTTAAAA | 29979 |
rs535195377 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83701796 | GAGCTTTGACCCAGC[A/C]ATTTCCACTCCAAGA | 29979 |
rs535307831 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83676359 | TGGTTTTTGGTTTTT[C/T]AGACAAAAGTTATTA | 29979 |
rs535356844 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83679323 | CTCAGCTCATGAGAA[C/T]ACTCTATTTTATAAA | 29979 |
rs535403080 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83690047 | AAGTATAAATCAGTA[A/C]ATTTTGGAATAACAT | 29979 |
rs535411962 | in-del | -/A | 0.00478657 | 0.0486865 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83678625 | ATTTCCAAAAAAAGA[-/A]AAAAAAAAAGGCATT | 29979 |
rs535415812 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83682631 | CCTTTTACAAATGAA[A/G]AAATTATTATTCAGG | 29979 |
rs535425849 | snp | A/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83676032 | AATACCTGAAGTATT[A/T]TCTGACCCTTCACAT | 29979 |
rs535494010 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83709404 | GCTCCTCATTACCTG[C/T]TTTTCCCTGTCATGC | 29979 |
rs535533909 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83708168 | AGTTCATGGTTTTTT[C/T]CCACTCCTTTCACCA | 29979 |
rs535542351 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83662703 | ACCTACCAAGAGCCA[A/G]AAACTATGCTACGCT | 29979 |
rs535549871 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83702083 | ACATGATTCCACTTA[C/T]AACAAACGCCCAGAA | 29979 |
rs535555908 | snp | C/G | | | upstream-variant-2KB, intron-variant | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83709949 | GAGCCACAGGATCTC[C/G]GTCTAAAACACTAAG | 29979 |
rs535654109 | in-del | -/A/AA | 0.00557806 | 0.0525533 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83690744 | AACCAGACTCTGTCT[-/A/AA]CAAAAAAAAAAACAA | 29979 |
rs535692362 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83698344 | GTCACTAGCTACATA[C/T]GGCTATTAAGCACCT | 29979 |
rs535831811 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83670892 | GCTCATCTACAAAAA[A/G]CAACTCCTCATCTGT | 29979 |
rs535874906 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83687163 | AAGTCCAAAGGAAGC[A/G]TAAAGGGAAGTCAGG | 29979 |
rs535926202 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83679156 | TCCCCCCCAAAACCA[C/T]AGTAAGCTGCAGTCA | 29979 |
rs536076494 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83691002 | AATTAGCCAGGCATC[A/G]TGGCACACACCTGCA | 29979 |
rs536086433 | snp | C/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83679188 | CGTGAGTCACTGTAA[C/G]AAGAAAGAGTTCCCT | 29979 |
rs536127457 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83664187 | CTCATTCTGGGAGAC[C/T]GATGATCCCAGCAGC | 29979 |
rs536147196 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83706447 | ATTTGATGTTACACA[C/T]CTCACTGCTTCACAA | 29979 |
rs536157502 | snp | A/G | | | upstream-variant-2KB, intron-variant | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83710241 | GAGCATACAAGAATA[A/G]TAAGACTCAGTTTCT | 29979 |
rs536236226 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83666737 | AAACGTGAATATATG[C/T]CATTGAAAGAAAAAT | 29979 |
rs536251380 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83662247 | GCAGAAAAACCTGTA[C/T]GTGTGTGTGTATATA | 29979 |
rs536270066 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83681349 | AGAGACTGTGTTACA[C/T]ATGTATTGAGAATAA | 29979 |
rs536372765 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83688145 | TTTGTAAGAATTAAA[C/T]GAGAATGTATATAAA | 29979 |
rs536410720 | snp | G/T | 0.00159617 | 0.0282053 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83707888 | CCGGGTCAGGCGCTC[G/T]GCAGCCGCCGTGTGT | 29979 |
rs536429839 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83668846 | TAACATTGCTCTTAA[C/T]TGCTTTCAAGATTTA | 29979 |
rs536479002 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83707810 | CCGCCTCAGTAGCAA[A/C]GGGCGCAGGGCCACC | 29979 |
rs536482509 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83668992 | TGGCAGAGATAAAGT[C/T]GTTTTAATTACATAT | 29979 |
rs536516164 | snp | A/C | 0.000798403 | 0.0199641 | downstream-variant-500B | UBQLN1 | GRCh38.p7 | 9:83659674 | ATCGCCCAGTCCAGC[A/C]CACCTATAAGCCTCA | 29979 |
rs536724817 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83694903 | AAGCTCCTTACCCAT[A/C]ATCAGATTTCTCCAA | 29979 |
rs536731433 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83686976 | CCAAGTCTGTCTGTT[A/T]AAAAAAAAAAAAAGT | 29979 |
rs536733002 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83666670 | GTTATGATAATGACA[C/T]GCAATATCCTAAAAA | 29979 |
rs536747066 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83690685 | GCTGCAGTGAGCTAC[A/G]ATCGTGCCACTGCAC | 29979 |
rs536785373 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83680568 | AAGAAAACTCAAAAT[A/G]AAAAGCACATCTGAG | 29979 |
rs536787833 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83683333 | AGGAGAATGGCGTGA[A/G]CCCAGGAGGCGGAGC | 29979 |
rs536825447 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83707196 | TTGTGAGGAGTTGGA[A/G]GGGAGGCGACGGAGG | 29979 |
rs536840495 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83664374 | AAGTGAGCTGAGATC[A/G]CGCCACTGCACTCCA | 29979 |
rs536996691 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83678172 | GACTACAGGCGCCCA[C/T]CACCACGCCCAGCTA | 29979 |
rs536996700 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83671082 | GGGATCCTCCTGCCC[A/C/G]AACCTTCCAAAGTGC | 29979 |
rs537029662 | snp | G/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83694098 | TTCAAAATCCAAACA[G/T]CCAAACTTGCTTTTA | 29979 |
rs537053660 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83683783 | ATCCCAGCACTTTGC[A/G]AGGCCGAGGCAGGCG | 29979 |
rs537156311 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83688733 | GGGCATTGTGGTGCA[C/T]GTCTGTAATCCCAGC | 29979 |
rs537269033 | in-del | -/TCTCTT | | | intron-variant, cds-indel | UBQLN1 | GRCh38.p7 | 9:83668628 | TTTTCTTAGCTGTGG[-/TCTCTT]TCTCTTTAGAAACAA | 29979 |
rs537278566 | snp | C/T | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83710203 | TTTTATCACAGTATC[C/T]TAATACTGTATAATA | 29979 |
rs537327664 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83692619 | GCACTTTGGGAGGCC[A/G]AGGCAGGCGGATCAC | 29979 |
rs537527117 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83664903 | ATAGCCTAGGCGAAG[G/T]GCGAGACCCTGTATC | 29979 |
rs537536063 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83707111 | ACAAAACCGCAGCCT[A/G]AGCTAAAGCGAACCC | 29979 |
rs537555139 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83706922 | CTATTACTTAAGATG[A/G]AGCTAAAAACAGTTT | 29979 |
rs537671703 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83678876 | GCGCCCGCCACCACG[C/T]CCCGCTAATTTTTTT | 29979 |
rs537751668 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83698229 | TGATATTTGAGGGTA[A/G]GGGAAGAGACAATAC | 29979 |
rs537789820 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83688541 | CATTTTATTGTATTT[G/T]AGGATTTGAAGGTAA | 29979 |
rs537790702 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83685564 | AGTCCCAGGCTGACA[A/T]GGGAGCATCACTTGA | 29979 |
rs537821155 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83704583 | TGTAATCCTAGCACT[C/T]TGGGAAGCCGAGGCA | 29979 |
rs537836523 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83669380 | AATACTTAAACAAAA[A/G]TTAAAGCTTTAAAAT | 29979 |
rs538046007 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83689048 | GAACATTTTCATTAC[A/C]TCAAAAAAATCTATA | 29979 |
rs538129500 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83662816 | GCCAGGCTCACGCCT[A/G]TAATCCCAGCACTTT | 29979 |
rs538301768 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83675291 | TCCAACAACCAAACA[C/T]TGAATTACTATATGA | 29979 |
rs538303660 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83682569 | TCCCAGACCCCCTTC[C/G]ATGTGTTCAGGACAG | 29979 |
rs538391570 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83676048 | TCTGACCCTTCACAT[C/G]AAAAATCTGTCAACT | 29979 |
rs538531221 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83702421 | ACAATGATCTCACAG[A/G]CATTTTTTTTCTCAG | 29979 |
rs538539974 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83663199 | AAGGAGAAAGGGAAA[A/G]AAAAAAGAAACCCAG | 29979 |
rs538596873 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83666575 | AAAAAAAGGAAAAGG[A/G]AAGATACTGTCCACA | 29979 |
rs538768406 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83668980 | CTAGTCAATGAATGG[C/T]AGAGATAAAGTTGTT | 29979 |
rs538851937 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83699544 | TCCAGGAGGTGGGGG[C/T]TGCAGTGAGCCATGA | 29979 |
rs538917844 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83695070 | AGATAAAGAAAATTG[C/T]GGGTGGTTGACCCCA | 29979 |
rs538921853 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83689996 | GAGCGTTACAGAGGA[C/T]GCAGAGCAACTGGAA | 29979 |
rs538997049 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83681264 | TTACCACAAAGTGTT[C/T]ACTTCGTAAAATTAC | 29979 |
rs539070742 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83690052 | TAAATCAGTACATTT[G/T]GGAATAACATTTTGC | 29979 |
rs539157201 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83696485 | AAAAAAACCCAATAA[C/G]AAAAATAGCTGGGCA | 29979 |
rs539333471 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83683285 | GGCGTGATGGCGAGT[G/T]CCTATAGTCCCAGCT | 29979 |
rs539378459 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83677080 | ATCTGATTTTTAATA[A/T]ACCTGGCAGGTGCTC | 29979 |
rs539395887 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83683749 | TTATCTTGGCCAGGT[A/G]CGGTGGCTCACGCCT | 29979 |
rs539427186 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83664851 | TTGAGCCCGAGAGGT[C/T]GAGGCTGCAGTGAGC | 29979 |
rs539462745 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83704301 | TTTGTGCTTCAAGTA[A/G]ATTTTACAAATAGGT | 29979 |
rs539581441 | in-del | -/AAAAAAAAAA | 0.283158 | 0.247791 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83664924 | ACCCTGTATCCCACC[-/AAAAAAAAAA]AAAAAAAAAAAAAGG | 29979 |
rs539739378 | snp | G/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83679011 | CAAGCGTGAGCCACC[G/T]CGCCCGGCCAGGAGG | 29979 |
rs539819748 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83699764 | AACTTTCTGTTACGG[A/G]CTAGACAGTAAATAT | 29979 |
rs539874132 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83670966 | GCTCCACCTCTTTTT[C/T]TCTTTTTAAATTGAG | 29979 |
rs539883890 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83693726 | TTCTCAATTGTTTTT[C/G]AGAAGAAAATAAGAC | 29979 |
rs539979534 | in-del | -/TT | 0.0293573 | 0.117545 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83693467 | TTTTTCTTTTTCTTA[-/TT]TTTTTTTTAACCAGA | 29979 |
rs540008093 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83701723 | TTGCTAGTGGAAATG[C/T]AAAATGGTACAGACA | 29979 |
rs540102946 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83698425 | ATATTTCAAAGACTT[A/T]GTATTTCAAAATGCA | 29979 |
rs540109498 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83666959 | CAAAAAAATAACACC[A/G]CAAAACAGCAACCAA | 29979 |
rs540211431 | in-del | -/AGT | 0.00119737 | 0.0244387 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83700980 | GTCAGGCAACTGACC[-/AGT]AGTAGGCTACTGCAG | 29979 |
rs540246883 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | UBQLN1 | GRCh38.p7 | 9:83660670 | CCGCTGCCCCACCCC[C/T]CCACCCCGTCCCCCT | 29979 |
rs540360589 | snp | A/G | | | downstream-variant-500B | UBQLN1 | GRCh38.p7 | 9:83659947 | TTTTTTCTTTCTACA[A/G]AAGAGGCAAGACAAA | 29979 |
rs540383032 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | UBQLN1 | GRCh38.p7 | 9:83660992 | GTGTTCCTTCAGTCT[A/G]CACAAAGATTAAGGT | 29979 |
rs540390085 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83687220 | AGAAAGACTACTAAA[A/G]AAAGTAGCCGATAAA | 29979 |
rs540422950 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83695150 | TGGACAGAATCACCC[A/C]AAAAAAAAAAAAAGT | 29979 |
rs540439865 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83688128 | AATGGCAGAACACAT[A/G]GTTTGTAAGAATTAA | 29979 |
rs540475017 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | UBQLN1 | GRCh38.p7 | 9:83661461 | ATTCTACATAAATTA[C/T]TACCATAGGCTAATG | 29979 |
rs540524585 | snp | G/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83678291 | CTCCCAAAGTGCTGG[G/T]ATTACAGGCGTGAGC | 29979 |
rs540531755 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83686594 | TCCTTATTCTTTTTA[C/T]GTTAATGAGACCAAA | 29979 |
rs540559808 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83701442 | AACATCTCAGAATTA[C/T]TATGAAAATAGTTTC | 29979 |
rs540596661 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83706860 | GAAAGAGCAAGTCAT[A/C]AGTGAAAGAAAGTCA | 29979 |
rs540635891 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, utr-variant-3-prime | UBQLN1 | GRCh38.p7 | 9:83668375 | TCCTGACACACTACA[A/G]AAGCCATTTTTAACG | 29979 |
rs540659239 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83707250 | GAGGGTCGGCGGATA[C/G]CAGAGAAGGAAGGCT | 29979 |
rs540720739 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83674388 | ACTCATCACAATACT[C/T]CCCACTCACAGAAAA | 29979 |
rs540734740 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83686340 | GAGGCTGCAGTGAGC[C/T]ATTATCACACCACTG | 29979 |
rs540746519 | in-del | -/CAAAAA | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83673568 | AAAAAAAAAAAAAAA[-/CAAAAA]AAAAAAACTGCGCTT | 29979 |
rs540794255 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83701846 | AAAACGTTATGTCCC[C/T]ACAAAAACTTATACA | 29979 |
rs540806271 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83674123 | TCGTACTGTTGTTCA[A/G]TATACTACTACAAAA | 29979 |
rs540841975 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83704501 | CATCAGAAAAGGCTA[C/T]TTCAGAAAGACTTTA | 29979 |
rs540862697 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83691289 | CAGACCAGACTGGAT[A/G]TAAGACATGAAAATG | 29979 |
rs540905122 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83698591 | AAAATGTGGTACATA[C/T]ATATAATGGAATATT | 29979 |
rs541193623 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83691521 | AATCAGGGCTTTCTG[A/G]ACAGACTAAGGGCTT | 29979 |
rs541331430 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83693482 | TTTTTTTTTTAACCA[A/G]ACTGTCAAGTTCTTG | 29979 |
rs541382014 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83687992 | TAACTAACAGAAAAT[C/G]TTCACAGAACACCAT | 29979 |
rs541464964 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83681775 | GAAATGCCAAAGGAC[C/T]ACAAGAAATGATATA | 29979 |
rs541520990 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83695113 | AAGGTAAAAATTATA[C/T]ATGAACATATAAATA | 29979 |
rs541750609 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83674733 | TTCTTGATAAGCTGA[C/T]AGATGTTACTGATAC | 29979 |
rs541806627 | in-del | -/AAG | 0.00279162 | 0.0372561 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83668710 | GGAATCAATAGTTGA[-/AAG]AAGGAGAACATTGTT | 29979 |
rs541896089 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83705855 | AAAGCCTTACCCAGA[A/G]AAATACACACAGTAC | 29979 |
rs541946201 | snp | G/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83675023 | TGTCTTATTCATCAG[G/T]AGGTACTCTGGAAAA | 29979 |
rs541959475 | snp | G/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83703513 | TTATGTATATACAAA[G/T]ATTCCAAAATCCAAA | 29979 |
rs541969202 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83702055 | GCTAAGTGAAAGCCA[A/G]TCACAAAAGACCACA | 29979 |
rs542061329 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83676660 | TGATCATTAATTACT[C/G]TTCTCATTCTGATTC | 29979 |
rs542100781 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83682352 | AGGCCAGGCACAGTG[G/T]CTCTCATCTGTAACC | 29979 |
rs542173097 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, missense | UBQLN1 | GRCh38.p7 | 9:83668607 | CAGCCAGCATTAAGA[A/T]CCCCAATTTTCTTAG | 29979 |
rs542176576 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83702442 | TTTTTCTCAGATATC[C/T]TGCTATACTGATTCA | 29979 |
rs542217918 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83696248 | TATGTAAACAATGTG[C/G]AGTGACTAAATCAAG | 29979 |
rs542314754 | snp | C/G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83708320 | CTGTCCAGGTAGTCT[C/G/T]CCCACCTTACCTCAT | 29979 |
rs542377384 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83680700 | GCATTTGTCTGTTTC[C/T]GAGTTGTATCCTTTA | 29979 |
rs542399557 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83690289 | TGCCACATATCATCA[C/T]GGATACCTCAACACG | 29979 |
rs542476470 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83686539 | ACATATCCTATATTC[C/G]ATCCTCTGCTAAGGC | 29979 |
rs542666526 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83665229 | TCTCTGTTATGCTTC[C/T]GGAGAAAATCTAAAA | 29979 |
rs542678052 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83699218 | TTAATGTCACTGAAG[A/T]GAACCCTTAAAAATG | 29979 |
rs542715588 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83704566 | GCCCGGTGGTTCACA[C/T]CTGTAATCCTAGCAC | 29979 |
rs542721113 | snp | C/T | | | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83707872 | AGGCTCTGGCGCAGG[C/T]CCGGGTCAGGCGCTC | 29979 |
rs542745697 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83673260 | AAAACAATTTTTGGT[C/T]GGGTGCAGTGACTTA | 29979 |
rs542748815 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83679565 | ATTCTTAAGCCTTCA[A/T]AATAAACTATTTACA | 29979 |
rs542764577 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83685864 | CACTTTTTAAAAAAA[A/T]TGTTATCGACAGCAA | 29979 |
rs542813754 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83679010 | ACAAGCGTGAGCCAC[C/T]GCGCCCGGCCAGGAG | 29979 |
rs542847802 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83694687 | ATGCTAGGATAGATA[C/T]ACTTCCTTCTATTGC | 29979 |
rs542872349 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant, utr-variant-3-prime | UBQLN1 | GRCh38.p7 | 9:83667654 | TATCACACATATCTT[G/T]TGGAATTCACTTCAT | 29979 |
rs542996371 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | UBQLN1 | GRCh38.p7 | 9:83660486 | AAACAGAATTCTTTG[A/G]GGGAGGGAAGAAAAA | 29979 |
rs543052747 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83706228 | GCAACTTACTCTGAA[C/T]TGCTCCCCAAAATTA | 29979 |
rs543147571 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83664597 | TCTCTTAATAAATAA[A/G]TAAGTAAATAAATAA | 29979 |
rs543147865 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83676571 | TGGTATTACTTCAGG[A/T]TTTACAAAACCTATA | 29979 |
rs543185100 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83703319 | CCATGACATCACATG[C/T]GGAAAAATCCCATAT | 29979 |
rs543200496 | snp | C/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83691722 | GTGAGAAATCACGTT[C/G]ACTCACAAAATTACA | 29979 |
rs543264614 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | UBQLN1 | GRCh38.p7 | 9:83660044 | CTATCCCACACTGAA[C/T]ACCACCATTTGCCAG | 29979 |
rs543271257 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83670559 | TAAAAAAAAACTCTG[C/T]ACATAAATATAAAAA | 29979 |
rs543308867 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83662988 | GGCTAAGGTGGGAGG[A/C]TTGCTGCAGCCCAGG | 29979 |
rs543489930 | snp | C/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83693570 | GCAGCAAATAATTAA[C/G]AGAAGTTAGAAAACC | 29979 |
rs543708795 | snp | A/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83672021 | CTTGTACCTTTACAT[A/T]ATGGAGTTGGCTTCT | 29979 |
rs543709797 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83708996 | TACAAACCAGCCCAT[C/T]ATTAATCAATGTTGC | 29979 |
rs543743998 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83663663 | TGTCTTCTCTACAAC[C/T]GTAACAACGTTTCCT | 29979 |
rs543754198 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83691144 | CTCGTCTCAAAAAAA[A/T]AAAAAAAATAAAAAA | 29979 |
rs543817111 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83683938 | AGGCAGGAAGACTAC[C/T]TGAACCCAGGAGGCG | 29979 |
rs543880858 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83687269 | CAGGGACCAGACACA[A/T]AAAACCAGACAAGAG | 29979 |
rs543896193 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83700535 | AATTTTTAGTTGTGA[C/T]GAATTCTTATCAAAA | 29979 |
rs544071605 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83666529 | AAGTGCCTCAGCTGG[C/T]ACTTAAAAGGGAGGA | 29979 |
rs544159842 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83678316 | GTGAGCCACTGCACC[C/T]GGCCACTGAACTTTT | 29979 |
rs544163350 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83702200 | ACAGCGTTTCTTTTT[C/G]AGGGTTCTAAACGTT | 29979 |
rs544200632 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83678167 | GCTGGGACTACAGGC[A/G]CCCACCACCACGCCC | 29979 |
rs544265139 | in-del | -/AGG | 0.00119737 | 0.0244387 | utr-variant-5-prime, upstream-variant-2KB, cds-indel | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83707736 | GGGAGCAGGCGAGCA[-/AGG]AGGAGCCAGCAGACA | 29979 |
rs544334704 | snp | C/T | 0.000181571 | 0.0095264 | missense | UBQLN1 | GRCh38.p7 | 9:83677927 | TCACCAGAGGATGTA[C/T]TGCTCACCAAGGAAG | 29979 |
rs544400739 | in-del | -/TGGA | 0.0146759 | 0.0843953 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83697783 | TCTTATCCCACAGGC[-/TGGA]TGGAGTGCGATGGCA | 29979 |
rs544428888 | snp | C/G | | | upstream-variant-2KB, intron-variant, nc-transcript-variant | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83708331 | GTCTCCCCACCTTAC[C/G]TCATGCCCAGCTGGG | 29979 |
rs544435199 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83688721 | CAAAACTTAGCTGGG[A/C]ATTGTGGTGCATGTC | 29979 |
rs544501344 | snp | C/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83663155 | GGGAAAAGGGAAAGG[C/G]GAAGAGGAAGGAGGA | 29979 |
rs544514116 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83680827 | AGCTGGTCAGTCAGA[A/G]GTACAGATGGCCTAG | 29979 |
rs544550818 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83673780 | AACAGAAACTGTCTA[C/T]GGTACTGTCACTCCT | 29979 |
rs544552333 | snp | G/T | | | intron-variant, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83705973 | TGATGGAAAGGCCAA[G/T]TGACTGAAATGACTG | 29979 |
rs544562286 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83707876 | TCTGGCGCAGGCCCG[A/G]GTCAGGCGCTCGGCA | 29979 |
rs544585242 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83701479 | TGGTACCCTTAACAG[A/G]GTATGGGGACTCCCC | 29979 |
rs544742112 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83668937 | CTAACTCAACATATG[C/T]AGAAACAAACTAAAC | 29979 |
rs544772480 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83696583 | GATCAAGGTTGCAGT[A/G]AGCTGTGATCGCACT | 29979 |
rs544807997 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83704102 | CCTCTGGAGGTCTTC[A/G]GCTTACCCTCTGACC | 29979 |
rs544818931 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83685161 | AAATAGAAGGAATAT[A/G]TTGAATGAGTAAAGC | 29979 |
rs544910314 | in-del | -/AA | | | downstream-variant-500B | UBQLN1 | GRCh38.p7 | 9:83659484 | TAAATATTATCACTC[-/AA]TATGAGAACAATTTA | 29979 |
rs544979128 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83673856 | TCCCAGGCTGGAGTG[C/T]GGTGATGCCATCACA | 29979 |
rs544988769 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83703917 | CTTACAATTTACCCA[A/G]GAAGTTTAACGTAAT | 29979 |
rs544992411 | in-del | -/T | 0.00358779 | 0.0422022 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83695563 | AATATGTAAAAGGTA[-/T]TTTTTTAAATGTAAA | 29979 |
rs545047825 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83704537 | ATCTATTAACAATTC[A/G]TACTGGGCCGGGTGC | 29979 |
rs545130983 | in-del | -/AC | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83662271 | TATATACATATACAT[-/AC]ATACACACACACACA | 29979 |
rs545134042 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83678957 | TGATCTCCTGACCTC[A/G]TGATCCGCCCACCTC | 29979 |
rs545139994 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83691928 | CTGCATATGACTACC[A/G]TTCATAATTCAGTTC | 29979 |
rs545162189 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83685669 | TATGATTATCAATTC[A/G]TGGTTTGCTAAGGAG | 29979 |
rs545228106 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83706727 | ATATTCTGCATTCAC[C/T]CCGATTTTCTTTTAT | 29979 |
rs545357306 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83682435 | GTGAGCTATGGATGG[C/T]ATCACTGCACTCTAG | 29979 |
rs545395558 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83682797 | TCCCCAACTACTTCC[A/T]TAATATCTACAATTA | 29979 |
rs545407120 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83672515 | AATAGGGAGACCCAA[C/G]AAGAGGAAGAGAGAC | 29979 |
rs545439510 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83693958 | AATTTCCTGGGCACA[A/G]TTCATTCACTAAGAC | 29979 |
rs545482649 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83662895 | ACCTGGGCAACACGG[C/T]TGAAACCCCAGCTCT | 29979 |
rs545483563 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83675491 | AAAAAAAATCACAAG[A/C]AGCAAGACCTCCATT | 29979 |
rs545561824 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant, nc-transcript-variant | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83708350 | TGCCCAGCTGGGCCG[C/T]GTTCACCCCTCCGCG | 29979 |
rs545619304 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83702496 | TGTCCAGCAGAAATA[C/T]ATATAAGCCACAAGT | 29979 |
rs545623168 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83708966 | TTGGCTTTTAAAGAT[A/G]ACTTGCAAGGAATGT | 29979 |
rs545661964 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83673452 | CAGGAGGCTGAGGCA[A/C]GAGAATCTCTAGAAC | 29979 |
rs545769690 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83669063 | ATTGGAGACACAGTT[C/T]ACTTATTTTTCTAGT | 29979 |
rs545821772 | in-del | -/T | 0.493793 | 0.055364 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83682824 | TTATAGGAATGTATG[-/T]TTTTTTTTTTTTAAT | 29979 |
rs545881578 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83703186 | AAAATCTCATACACA[A/G]GGACTTTGTGCCACT | 29979 |
rs546035980 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83662939 | AAATTAGCCAGGTGT[C/G]GTGGTCTGCGCCTGT | 29979 |
rs546132530 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83697548 | CAGTGCAAGACACTG[G/T]CTCAAAAAAAAAAAA | 29979 |
rs546219716 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83677083 | TGATTTTTAATAAAC[C/G]TGGCAGGTGCTCTGA | 29979 |
rs546241148 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83695457 | CCCACCTCAGCCTCC[C/T]GAAGTGCTGGACTTA | 29979 |
rs546270254 | snp | A/T | 0 | 0 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83663491 | CAAAAGACAGACTAG[A/T]ATACAGCTGCCCTGG | 29979 |
rs546444063 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83678044 | TTTTTTTTTTTGAGA[C/T]GGAGTCTCGCTCTGT | 29979 |
rs546495225 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83683503 | ATCAAATTATCATTT[A/T]GTAAAAAGCCTGAGA | 29979 |
rs546558246 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83683898 | TGGTGGCACATGCCT[C/G]TAATCACAGGTACTC | 29979 |
rs546570595 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83685277 | AGCTCTTTTAAGCAA[C/T]GCTACACCACCAACA | 29979 |
rs546587874 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83678755 | GGAGTCTTGCTTTGT[C/T]GCCCAGGCTGGAGTG | 29979 |
rs546593112 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83693090 | TGCACTGATAACCTA[A/C]AATAACTACAGGCCA | 29979 |
rs546640755 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83699983 | AGTGAGAATATTTAC[A/T]TCATGGAAATCCAGC | 29979 |
rs546707446 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83692457 | ATAGTATTGATATGG[A/G]AAAACTTAATTAGCC | 29979 |
rs546717127 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime | UBQLN1 | GRCh38.p7 | 9:83660084 | TTTTAAACCAAACTG[A/C]GGCATAAAGCAGAAA | 29979 |
rs546740483 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83687417 | CCAGGAATCTACATT[A/G]AAAGACTGGCTCAAG | 29979 |
rs546758613 | in-del | -/TC | 0.00119737 | 0.0244387 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83689129 | CAGTAATTTCTACTT[-/TC]TGTTTCCATACGAGT | 29979 |
rs546848862 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83672235 | GCAATGAAGTTGTTT[C/T]GCTTTCTTGTCATTC | 29979 |
rs546854526 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83705490 | TCAGGCAATCCACCC[A/G]CCTCGGCCTCACAAA | 29979 |
rs546876898 | in-del | -/A | 0.0119091 | 0.0762411 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83705834 | ATTATGCTGAGTGGG[-/A]AAAAAAAAGCCTTAC | 29979 |
rs546999611 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83700776 | GTCAATGTAGTCAGC[C/G]AAGCAAGCAAAGAAA | 29979 |
rs547117775 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83706298 | ATTGTAGATGATGGA[C/T]ATATGTGTATCCACT | 29979 |
rs547128605 | in-del | -/A | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83686910 | AATATCCCAAAATCC[-/A]AAAAAAACAAAAAAA | 29979 |
rs547157716 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83662788 | TTTAGTAAGGCTTGA[A/G]AACAGAAAGCAGGCC | 29979 |
rs547163636 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83690728 | AACAGCTTGGTCAAT[A/G]GAACCAGACTCTGTC | 29979 |
rs547178250 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83702310 | TACACTTCAATTACG[C/T]TCTTTCTTAAAAAAA | 29979 |
rs547224986 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83683740 | AAAACTTTTTTATCT[A/T]GGCCAGGTGCGGTGG | 29979 |
rs547250150 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83683216 | AAGAGATAGAGAACA[C/T]CCTGGCTAACACAGT | 29979 |
rs547260236 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83694741 | GGTGAACAAAAGGCT[G/T]TGGGGAAAGAAACCA | 29979 |
rs547269442 | snp | A/C | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83704243 | GTAACAAACAGTTTC[A/C]ATCAAACCCTTTAAA | 29979 |
rs547384778 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83697679 | TTCCACCTCAGCTTC[C/G]CAAGTAGCTGGGACT | 29979 |
rs547438069 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83678138 | ACCATTCTCCTGCCT[C/T]AGCCTCCCGAGTAGC | 29979 |
rs547497981 | snp | A/C | | | missense | UBQLN1 | GRCh38.p7 | 9:83686107 | CAGCAAATATCAACA[A/C]AAGTTGGTCAGTATG | 29979 |
rs547536927 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83708459 | TAGCGGCGAGGTATT[C/T]TGTTATTTTAATATG | 29979 |
rs547639739 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83704593 | GCACTTTGGGAAGCC[A/G]AGGCAGGCGGATCAC | 29979 |
rs547813722 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83664254 | GACTTCATCTCTACA[A/T]AAAATAAAAACAAAA | 29979 |
rs547889730 | snp | C/G | | | synonymous-codon, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83707620 | GGCGCCAGCACCTTC[C/G]GCTCCGGCGGCGCTA | 29979 |
rs547935692 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83698423 | ATATATTTCAAAGAC[A/T]TAGTATTTCAAAATG | 29979 |
rs547956395 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83680172 | ATTTAAAAACAAATC[A/G]AATACCTATTACTAA | 29979 |
rs548097166 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83664843 | AGAATCCCTTGAGCC[C/T]GAGAGGTCGAGGCTG | 29979 |
rs548130222 | in-del | -/ATT | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83700852 | GGGCCTCGCTACTCC[-/ATT]ATTATATATTCTAAG | 29979 |
rs548135406 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83665416 | TTTGGAAGCCACAAC[C/T]ATTCCCCTTCTCCAA | 29979 |
rs548135824 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83681056 | ACACCAGACTATGCT[A/T]CTAATAATCTTTCCA | 29979 |
rs548175319 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83673555 | GTCTTTTAAAAAAAA[A/C]AAAAAAAAAAAACAA | 29979 |
rs548200727 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83697987 | GTGATCCACCCGCCT[C/T]GGCCTCCCAGAGTGC | 29979 |
rs548211749 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83707078 | GAGGATCCCACCCAC[C/G]CCTTTTTAATTCATG | 29979 |
rs548218145 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | UBQLN1 | GRCh38.p7 | 9:83660963 | TAGGCAAATGCACTT[C/T]GGGGTATACTACAGT | 29979 |
rs548356801 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83692499 | TCTCAAAGCTGTTTA[A/G]ACAGAGGTAGCTCAC | 29979 |
rs548381617 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | UBQLN1 | GRCh38.p7 | 9:83661540 | CAACTATAAAAGGTG[A/G]TGTTTTTAAAAAATT | 29979 |
rs548539734 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83708187 | CTCCTTTCACCAAAA[A/C]CTAAATCGCAGTTTC | 29979 |
rs548540766 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83694698 | GATATACTTCCTTCT[A/G]TTGCAAAAACTTAAA | 29979 |
rs548576602 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83688260 | GAAGAGAGTTTTTAA[C/T]CCTATTTCAGACACA | 29979 |
rs548579272 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83675005 | AAGACTATAGTTATT[C/G]ACTGTCTTATTCATC | 29979 |
rs548637920 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83688810 | AGGTTGCAGTGAGCC[A/G]AGATTGCACCATTGC | 29979 |
rs548772409 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83672134 | TAAAGAGAGTTAGGG[C/G]CTTGCTCTGGATTAG | 29979 |
rs548842426 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83682517 | CAAACAAAAACTAAT[A/G]TAAGAAAAACAAAAG | 29979 |
rs548873566 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83678650 | GGCATTGAAATACAC[A/G]TGAATTACATTAATT | 29979 |
rs549002505 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83685205 | TGGTAAACAACAGCA[C/T]AAAAACTTACAGGAG | 29979 |
rs549015676 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83699399 | ACAGCTGGAATGCTG[C/T]GGTGCAATCATAGCT | 29979 |
rs549056655 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83665574 | GTAAGGTACACTCTA[A/T]AACAACAGTTCCAAA | 29979 |
rs549058707 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83672677 | ACCACAACAGAATAA[C/T]GAAAAAGCCTGAAAT | 29979 |
rs549095846 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83705445 | AGTAGAGACGGGGTT[G/T]CACCCCGTTGGCCAG | 29979 |
rs549136418 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83693951 | ATACGGAAATTTCCT[C/G]GGCACAATTCATTCA | 29979 |
rs549239419 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83678173 | ACTACAGGCGCCCAC[C/T]ACCACGCCCAGCTAA | 29979 |
rs549244564 | snp | A/C | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83663695 | TAGTGTCTCAGCACC[A/C]AAGTCAACAATTTTT | 29979 |
rs549252296 | snp | C/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83684293 | TCCACCTCCCAGGTT[C/G]AAGCGATTCTCCTGC | 29979 |
rs549277277 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83693428 | TGATAACTGTCCAGA[C/T]TCTCAAGGTATCTTG | 29979 |
rs549328422 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83689716 | ATTGTTTTAAAGGGG[C/T]ACCATATACTGGACT | 29979 |
rs549333363 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83706808 | CAAAAACCTACCCAA[C/T]GATTGGCATCTAAGA | 29979 |
rs549344515 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83687147 | GTCAAGTAAAACCAT[A/G]AAGTCCAAAGGAAGC | 29979 |
rs549391211 | snp | C/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83687229 | ACTAAAGAAAGTAGC[C/G]GATAAAACCTGAAGA | 29979 |
rs549461043 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83675642 | TACCTTTCACTTTGA[A/G]GTGATTAATCTGAAT | 29979 |
rs549480589 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83704792 | CACCATGCCATTGCA[C/G]TCCAGCCTGGGGGGT | 29979 |
rs549515608 | snp | A/G | | | upstream-variant-2KB, intron-variant | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83709080 | GCCTTTCTGCTCCTA[A/G]GCCGTCCAACCCTGT | 29979 |
rs549527720 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83686336 | GTTCGAGGCTGCAGT[A/G]AGCTATTATCACACC | 29979 |
rs549536381 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83696993 | GTTGCCCAGGCTGGC[A/G]TGGAACTCTTGGGCT | 29979 |
rs549559933 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83682020 | AGCCACTGAGTTTGG[C/T]TATCTATTATCAAAA | 29979 |
rs549631010 | snp | C/T | 0.00378727 | 0.0433508 | utr-variant-5-prime, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83707694 | TGGCTGTGGCGGCGG[C/T]GGCGGCGGTGACTCA | 29979 |
rs549671344 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83696373 | TAAGAATAAACACAC[A/T]TTTTCAAAATCACAT | 29979 |
rs549673482 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83702749 | GATGGTATCAAAGTG[A/G]ACAGTATAGTTCTAG | 29979 |
rs549736298 | snp | A/C | 0.000798403 | 0.0199641 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83708104 | CATTGCCCAAAGTGC[A/C]GGCGAAGCCAGTGTG | 29979 |
rs549767655 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83662649 | ATTCTAATACTCCAA[A/C]TCCTTCTTTCTTATT | 29979 |
rs549930649 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83683348 | ACCCAGGAGGCGGAG[C/T]TTGCAGTGAGCGAGA | 29979 |
rs549957480 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83688578 | AGATTAAACACATGC[A/G]TCGGGCGGGGTGCAG | 29979 |
rs550093975 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83709850 | TCTGGGAGGGCTAGA[C/T]AGTAAATATTTGGTT | 29979 |
rs550128850 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83664775 | TATATATAAATTAGC[C/T]AGGTGTGGTGGTGCA | 29979 |
rs550153196 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83704053 | TATAGAAAACGGAAT[C/T]TGTCTGATACAGAGC | 29979 |
rs550242383 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83683184 | TTGGGAGGCCGAAGC[A/T]GGCTGATCACGAGGT | 29979 |
rs550367285 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83688849 | CTGGGCGATGAGAGC[A/G]AAACTCCGTTTCAAA | 29979 |
rs550396005 | snp | A/G | 0.000583544 | 0.0170714 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83686171 | CTAAATAAAAATAAA[A/G]TAAGTATGTATTACA | 29979 |
rs550442425 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83697771 | GACGAAGTCTCACTC[C/T]TATCCCACAGGCTGG | 29979 |
rs550474794 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83709302 | AGATGATCACTGCTT[C/T]TAAAGCTAGAAAGTG | 29979 |
rs550490579 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83670835 | AATAATGTTCACAGC[A/C]TCTTCACTTACAGCA | 29979 |
rs550505187 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83686725 | TACACAGCCAATCTC[A/G]TATTCTTGGCCTAGC | 29979 |
rs550633131 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | UBQLN1 | GRCh38.p7 | 9:83667235 | ATAAGATTAAAATAC[A/G]CAAGGAGCATAACCA | 29979 |
rs550694558 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83692548 | GAAAAATAAAACTTA[C/T]TACAATTATACAAAA | 29979 |
rs550758138 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83670525 | CTGTAGTCTATTAAG[C/T]ATGCCACAGCCTTCG | 29979 |
rs550769304 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83674942 | GTGCAGAATTAAAAC[A/G]ACTTAGTTGGACATA | 29979 |
rs550835394 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83706958 | TCATAATTTTTTTTT[A/T]AAGGTTGCAAGGTGG | 29979 |
rs550839643 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83700118 | AAATTATATTCATTA[A/T]GAACCATCTTTGAAA | 29979 |
rs550844929 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83681280 | ACTTCGTAAAATTAC[A/G]TAACCAACTAAATGC | 29979 |
rs550890458 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83673478 | AGAACCTGGGAGGCA[C/G]AGGTTGCAGTGAGCC | 29979 |
rs551015768 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime | UBQLN1 | GRCh38.p7 | 9:83660814 | GAGAAAACAGATAAA[A/C]CCAAAAGATAGTTCT | 29979 |
rs551021438 | in-del | -/C | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83701578 | TCAGAGTGCCCCCAG[-/C]AAAAATAATAATGAA | 29979 |
rs551099088 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83700838 | GAACCGTATTACACA[G/T]GGCCTCGCTACTCCA | 29979 |
rs551114793 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83684367 | GCTGGGCAATTTTTT[G/T]TATTTTTAGTAGAGA | 29979 |
rs551252634 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83683750 | TATCTTGGCCAGGTG[C/T]GGTGGCTCACGCCTG | 29979 |
rs551288712 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83701118 | TTTACAACTTCAGAA[C/T]TCCAAAGAGTTTTGC | 29979 |
rs551309136 | snp | C/T | 0.0001319 | 0.00811989 | synonymous-codon | UBQLN1 | GRCh38.p7 | 9:83665059 | CGGGGCTTCCGTTGC[C/T]AATGTCTGTAAACCC | 29979 |
rs551386691 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83690778 | CAGAAACATCAAGAA[C/G]TCGAAACACAGCCAG | 29979 |
rs551528701 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83699332 | TAGGAAAATTACATA[C/T]GTGGCTCATACTGTT | 29979 |
rs551575881 | snp | A/C | | | utr-variant-3-prime | UBQLN1 | GRCh38.p7 | 9:83660106 | AAGCAGAAAGAGCAA[A/C]GACACATGAATACCC | 29979 |
rs551619187 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83671955 | TTGATGATCTTAGGA[A/G]ATCTTCTGGATAACT | 29979 |
rs551661430 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83705377 | GCCTCAGCCTCCCCA[A/G]TAGCTGGGATTACAG | 29979 |
rs551699093 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83698685 | TTTGGGAGACCAAGG[C/G]GGCAGATCGCTTGAG | 29979 |
rs551715911 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83693164 | ATAAGAATCAAAATT[C/G]TAATGCACCTTGAAT | 29979 |
rs551798896 | snp | A/G | 6.55372e-05 | 0.00572401 | synonymous-codon, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83707596 | CTCCGCGGAGGCAGC[A/G]GCCGCGGGGGCGCCA | 29979 |
rs551828154 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83681949 | GGCACCTTACAAACC[A/G]GTAAAAAGCGTAGCA | 29979 |
rs551850478 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83671540 | TCAAAGCTCTTGGGT[A/G]ACTACATGCACTGTC | 29979 |
rs551855805 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83681851 | AGCTGTCTCTTCTGC[C/T]GTGTTCCAAATGGTA | 29979 |
rs551920289 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83692571 | ATACAAAATATTTTC[A/G]GCCAGGCGCAGTGGC | 29979 |
rs552021909 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | UBQLN1 | GRCh38.p7 | 9:83668030 | AAAGCAAGATGCACA[C/T]TCAGTATTAGCCAAA | 29979 |
rs552032275 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83670003 | CTACTTCATAGGGTG[A/G]TTGTAAGAAAATTAA | 29979 |
rs552053737 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83708041 | GCCGAGTCATCCCCG[A/G]CTGGCGCGACTTTGA | 29979 |
rs552080233 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83695815 | CATGCCTATAATAAA[C/T]AGAATCTGTGAAGTA | 29979 |
rs552231170 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83700226 | AGAAGAGTAATGTTC[C/T]AGGCAGAGAAGCAAG | 29979 |
rs552375346 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83696291 | TCACCTCTCTTATCT[G/T]TTTTGTAGTTGCAGC | 29979 |
rs552459670 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | UBQLN1 | GRCh38.p7 | 9:83661722 | AATGAAATAAAGCAG[A/G]TATTTTAAAGTTTAA | 29979 |
rs552521236 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83670810 | AACATTCTGAATTCG[C/T]TGTCATTTCAATAAT | 29979 |
rs552600653 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83702855 | GCTCAATTTGACTCA[A/G]TACGTTTAAATTATG | 29979 |
rs552668145 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83678222 | GAGACGGGATTTCAC[C/T]GTATTAGCCAGGATG | 29979 |
rs552706524 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83671711 | AGAGCATAGGCAGAA[C/T]AGATCTAGCATAATT | 29979 |
rs552867413 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83670215 | ATATTCTCAAACTTA[C/T]TATGCCAAGTCAACT | 29979 |
rs552901660 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83676771 | TTAAAACATGCCCAG[C/T]CTATCTCATCTTAGA | 29979 |
rs552908095 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83671159 | ATTCTAGTTCTCTTG[C/T]TATTTCCACTACTTC | 29979 |
rs552914590 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83685753 | AAACTTGCCTGTTCT[A/C]ATGCAAATAATTTAG | 29979 |
rs552976090 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83686458 | ATCCTTTTTATGTCA[A/G]TATCTTGATGTTAGT | 29979 |
rs553091698 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83684522 | AGTATTATCTCTAAA[A/C]GGAAATAAGCCAGAC | 29979 |
rs553193429 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83692860 | TCCGTTTTAAAAATA[A/G]TAATAACAACAATAA | 29979 |
rs553194005 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83666616 | CAGAAGAACAAAAAC[-/A]AAAAAAATGAGGCAT | 29979 |
rs553237457 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83679340 | CTCTATTTTATAAAA[C/T]GAGGTGTTGTCTGAT | 29979 |
rs553251368 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83704506 | GAAAAGGCTACTTCA[A/G]AAAGACTTTAATTTT | 29979 |
rs553264550 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83673159 | CGTTTGAACCCAGGA[C/G]AAGAAGGTTGCAGTG | 29979 |
rs553296592 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83693491 | TAACCAGACTGTCAA[C/G]TTCTTGTCTTGAAAG | 29979 |
rs553303368 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83666838 | GAACTATGTAACATG[C/G]CTTGCTTAGAAACCT | 29979 |
rs553315220 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83688599 | CGGGGTGCAGTGGCT[A/C]ACACCTGTAATCCCA | 29979 |
rs553416198 | snp | C/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83665753 | ATACATGAGGCCCTA[C/G]AACTACCAGTTTCAA | 29979 |
rs553497663 | snp | C/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83696417 | CTAAGACCAGCCTGT[C/G]TGGGCAACATGGCAA | 29979 |
rs553534529 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83662355 | GTAGCTACTGACCAA[C/T]TGAGTAACTATAAAA | 29979 |
rs553537067 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83682353 | GGCCAGGCACAGTGG[C/T]TCTCATCTGTAACCC | 29979 |
rs553545614 | snp | A/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83674607 | TGTGTCCAGAGAAAA[A/T]AAACTCACTGAAGTC | 29979 |
rs553632358 | snp | A/T | 0.00874735 | 0.0655527 | intron-variant, downstream-variant-500B | UBQLN1 | GRCh38.p7 | 9:83667415 | CGTATTTAAGAGCAA[A/T]GTAAATGCTGGTAGA | 29979 |
rs553677773 | snp | C/G | | | intron-variant, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83707242 | AGGAGGCTGAGGGTC[C/G]GCGGATACCAGAGAA | 29979 |
rs553723912 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83676978 | TTTCTAACCTGTTCA[C/T]ACATGAGAATCTGCT | 29979 |
rs553765768 | snp | C/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83699670 | TTCTATAAAAAATAA[C/G]TCATGGTAAAAATTT | 29979 |
rs553867508 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83708762 | GTGTGTAGGGCGGAA[C/G]AGGGTGCCCGAGGAG | 29979 |
rs553917534 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83703710 | ATGTTACTCAGTTGA[C/T]TCTGAGTGCTCCGTG | 29979 |
rs554047632 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83682636 | TACAAATGAAAAAAT[C/T]ATTATTCAGGGACGC | 29979 |
rs554048682 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83669640 | ATTACTGCTGAAAAA[C/G/T]TCCATAAAGTGAAAA | 29979 |
rs554173105 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83697797 | GCTGGAGTGCGATGG[C/T]ACGATTCAGCTCACT | 29979 |
rs554273638 | snp | A/G | 0.00119737 | 0.0244387 | downstream-variant-500B | UBQLN1 | GRCh38.p7 | 9:83659697 | AAGCCTCACCACCAC[A/G]TGTATAATAAAGAAA | 29979 |
rs554285443 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83662894 | AACCTGGGCAACACG[A/G]TTGAAACCCCAGCTC | 29979 |
rs554566223 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83671191 | ACAGTCCCCTCCTCC[A/G]TAGAAGTCTTGAACC | 29979 |
rs554617084 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83673681 | TCAAATTTCAACGCC[C/T]ATGAATACCATTTTA | 29979 |
rs554779173 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83680600 | GTTAGGAGGGTTGTG[C/T]GCTGAGGAAACCTGG | 29979 |
rs554790812 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83694342 | TTCAAGAGTCTATTT[C/T]TGAATTAGCTCCTTA | 29979 |
rs554819001 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83690492 | CTTTAGGCTAAAACA[C/T]GAACCTGTACATTTA | 29979 |
rs554843034 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83701348 | TGGATTTTCACATCT[A/C/G]TTGTCATATCCCACA | 29979 |
rs554853735 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83687116 | ACTCTCCCTGAAGGT[G/T]AGCAGTCCAATGAGA | 29979 |
rs554871481 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83700275 | GTCAAGAGTTGTGCC[C/T]GGAGAGTGGTGACCT | 29979 |
rs554897262 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83677213 | AACTACACAGGTAAC[C/T]AGTAACAACTACACA | 29979 |
rs554977714 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83707204 | AGTTGGAGGGGAGGC[A/G]ACGGAGGGCGGGGAA | 29979 |
rs554984453 | snp | C/T | 4.94311e-05 | 0.00497123 | missense | UBQLN1 | GRCh38.p7 | 9:83677823 | CAGTGCTGGCAGTGC[C/T]GCTGGAAGCTGATGA | 29979 |
rs555034809 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83683789 | GCACTTTGCGAGGCC[A/G]AGGCAGGCGATCAAC | 29979 |
rs555108520 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83671666 | TGTCATCCAGGCTTT[C/T]TTTCTTTTTTTCTTT | 29979 |
rs555147544 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83664929 | GTATCCCACCAAAAA[A/G]AAAAAAAAAAAAAAA | 29979 |
rs555184867 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83701829 | TACACCCAAGAAAAA[A/T]GAAAACGTTATGTCC | 29979 |
rs555198671 | snp | A/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83676145 | CATCTTTACATGTGT[A/T]TGTGTGCATATATGT | 29979 |
rs555220944 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83671098 | AACCTTCCAAAGTGC[C/T]GTGATTAAAGGTATG | 29979 |
rs555329485 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83698908 | GACAAAGTGAGACCT[A/G]TCTCAAAAAAAAAAA | 29979 |
rs555389006 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83692628 | GAGGCCGAGGCAGGC[A/G]GATCACCTGAGGTCG | 29979 |
rs555464452 | in-del | -/T | 0.402645 | 0.197989 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83693468 | TTTTCTTTTTCTTAT[-/T]TTTTTTTTAACCAGA | 29979 |
rs555465384 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83698466 | TAGTCTTTATATCAA[C/T]TGCACCTTAAAATAT | 29979 |
rs555667046 | snp | A/T | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83709561 | ATTTAGAGATATGGT[A/T]TTTCCCTTGATTCTC | 29979 |
rs555721687 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83701715 | CTCATGCATTGCTAG[G/T]GGAAATGTAAAATGG | 29979 |
rs555723666 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83695057 | AGTAGAACGAGTAAG[A/G]TAAAGAAAATTGTGG | 29979 |
rs555786992 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83695884 | ATCAACTTCAGTCTC[C/T]AAAAAAAGCTCCTAA | 29979 |
rs555910688 | snp | C/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83673655 | TGTGAAACGTGAAAA[C/G]TATATGAAATTCAAA | 29979 |
rs555934185 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83682521 | CAAAAACTAATATAA[A/G]AAAAACAAAAGCAGT | 29979 |
rs556016979 | snp | C/G/T | 0.00119737 | 0.0244387 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83705563 | GCATTTTTTAAAACA[C/G/T]AGTTTCTCACAAAAC | 29979 |
rs556018764 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83679359 | GTGTTGTCTGATTCT[A/G]GAATCACAAATAAAA | 29979 |
rs556036723 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83672485 | CTGACCCAATTTCAA[C/T]GTTGTGTCTCAGAGA | 29979 |
rs556074919 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83685549 | GTGGCACGCACCTAC[A/G]GTCCCAGGCTGACAT | 29979 |
rs556092527 | snp | C/G | | | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83707977 | CCTTCCCCCACGTCC[C/G]TTCGCCGGCGCCGCG | 29979 |
rs556181366 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83707119 | GCAGCCTGAGCTAAA[A/G]CGAACCCTCGCCCCC | 29979 |
rs556220384 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime | UBQLN1 | GRCh38.p7 | 9:83661280 | AGTATGTTTCCAGAA[A/G]TGCAGTCCCAAATGT | 29979 |
rs556278307 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83682291 | CTCTGTCTCAAAAAA[A/T]ATATATATATATATT | 29979 |
rs556406105 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83669866 | AGAGCACAGTGACTC[C/T]AAGCAGTATCAGGAG | 29979 |
rs556438518 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83675324 | TCGTTTTTGTTAGAG[A/G]GTTGGTAATGCTTAT | 29979 |
rs556515400 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83708251 | GTCACGGTTAGCGAA[A/C]TTACTAGAAAGGGAC | 29979 |
rs556525549 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83662839 | AGCACTTTGGGAGGC[A/C]AAGGCGGGTGAGATC | 29979 |
rs556537038 | snp | C/T | 0.00398564 | 0.0444627 | upstream-variant-2KB, intron-variant | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83708701 | GTATTGACAGTGGCC[C/T]CTGCTGCTACGATGA | 29979 |
rs556691892 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83665900 | TAATCTTACTAATCC[C/T]GAGTTTGAGGAAATG | 29979 |
rs556740283 | snp | G/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83685479 | AGTTAGCAGTATTCT[G/T]TCTTAGTGATACACA | 29979 |
rs556858992 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83702423 | AATGATCTCACAGAC[A/T]TTTTTTTTCTCAGAT | 29979 |
rs556892638 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83679474 | ACCTCAAAAAAGCAA[C/T]TTAGCATTCAAATAA | 29979 |
rs556920523 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83703056 | CCTCCATTATCTGCA[C/T]TAATGTCTCACATAT | 29979 |
rs556965453 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83672301 | AAGAACTTTTCCTTC[A/G]CATTCACAACTTGGC | 29979 |
rs557103384 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83674343 | TGACACTAAAAGAAT[A/C]CAACATATATAAGCA | 29979 |
rs557177468 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83699550 | AGGTGGGGGCTGCAG[G/T]GAGCCATGATCACTG | 29979 |
rs557215509 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83666588 | GGGAAGATACTGTCC[A/C]CAAGAGGGATCTCCA | 29979 |
rs557239513 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | UBQLN1 | GRCh38.p7 | 9:83667589 | CTTAAGGTCAACAAA[A/C]CTGCTTCTTTATTGG | 29979 |
rs557269842 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83698439 | TAGTATTTCAAAATG[C/T]AAGATATTTTATAGT | 29979 |
rs557272121 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83706730 | TTCTGCATTCACTCC[C/G]ATTTTCTTTTATTTG | 29979 |
rs557289279 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83682824 | ATTATAGGAATGTAT[G/T]TTTTTTTTTTTTAAT | 29979 |
rs557292966 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83686955 | AAATCTGAGACACTT[C/T]TGGTCCCAAGTCTGT | 29979 |
rs557423192 | snp | C/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83679541 | CCATCTCCAGCATTG[C/G]ACTTTTTGATTCTTA | 29979 |
rs557435415 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83690069 | GAATAACATTTTGCA[A/G]CAGAAGTTGAACATA | 29979 |
rs557527150 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83708967 | TGGCTTTTAAAGATG[A/C]CTTGCAAGGAATGTA | 29979 |
rs557540209 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | UBQLN1 | GRCh38.p7 | 9:83668107 | TAACAACTCAGTCTG[A/G]TAAGTTTCATATGCA | 29979 |
rs557771913 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83698426 | TATTTCAAAGACTTA[A/G]TATTTCAAAATGCAA | 29979 |
rs557868266 | snp | A/T | 0.0444908 | 0.142359 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83682289 | GACTCTGTCTCAAAA[A/T]ATATATATATATATA | 29979 |
rs557916331 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83685001 | ACTACATGCCTGCAC[A/G]TGTAGTCTACATGAC | 29979 |
rs557931148 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83709502 | ACCTGTCTAACTTCT[A/C]CTCATCCTGTATCAC | 29979 |
rs558094175 | snp | C/G | 0.0119091 | 0.0762411 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83674029 | GTCTCAAACTCCTGG[C/G]CTCAAGCAATCCACC | 29979 |
rs558116526 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83697960 | AGGCTGGTCTCAAAC[C/T]CCTGACCTCATGTGA | 29979 |
rs558176203 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83691095 | GTGAGCCAAAATCGC[A/G]CCACTGCACTCCAGC | 29979 |
rs558185115 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83705880 | CAGTACTATAGGCTC[C/T]ATGGGATCCCATTTA | 29979 |
rs558249049 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83700385 | TTCAACAATAAGTAG[G/T]TATTACTGAATATGT | 29979 |
rs558360570 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83685499 | AGTGATACACAAAGG[C/T]ATCTCTTTAAAACTG | 29979 |
rs558418406 | snp | A/C | 0.000399281 | 0.0141238 | downstream-variant-500B | UBQLN1 | GRCh38.p7 | 9:83659808 | TATCTTTTTATCACA[A/C]CACAAAAGACTGTGA | 29979 |
rs558433250 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83678300 | TGCTGGGATTACAGG[C/T]GTGAGCCACTGCACC | 29979 |
rs558491584 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83685955 | GTTACTTTTAGAAGT[A/G]CGAACATTTATCCAC | 29979 |
rs558565490 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83700986 | GCAACTGACCAGTAG[A/G]CTACTGCAGTTTCTA | 29979 |
rs558629618 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83697772 | ACGAAGTCTCACTCT[C/T]ATCCCACAGGCTGGA | 29979 |
rs558635818 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83695299 | CACCTCCCGGGTTCA[A/G]GTGATTCTCCTGCCT | 29979 |
rs558672422 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83687644 | GGACAAGGAAGGGAA[A/G]GCATATATAAAAAAC | 29979 |
rs558814418 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83688505 | ATAAGTGACTTAATT[A/G]CTGAACATACAGTTA | 29979 |
rs558824801 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83662161 | ATGTCAAATAGATCA[C/T]GACTCTACTTTAGGG | 29979 |
rs558827369 | snp | A/C | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83671073 | TAGGCTCAAGGGATC[A/C]TCCTGCCCGAACCTT | 29979 |
rs558851643 | in-del | -/CTG | | | cds-indel | UBQLN1 | GRCh38.p7 | 9:83663920 | CATCTGCTGAATAAA[-/CTG]CTGATGTCCAGGTTC | 29979 |
rs558858426 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83662801 | GAAAACAGAAAGCAG[A/G]CCAGGCTCACGCCTG | 29979 |
rs558895936 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83687223 | AAGACTACTAAAGAA[A/T]GTAGCCGATAAAACC | 29979 |
rs558922870 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83668911 | GCATTCCAGAACTCT[A/G]TACTTGTCTCCTAAC | 29979 |
rs559168028 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83670786 | CTGCTTTATCAACAA[A/C]GTTTATGAAACATTC | 29979 |
rs559175819 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83702375 | AACGAGTTTTTCAGC[A/T]GTCCAGTATTAGAAC | 29979 |
rs559247762 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83707838 | ACCGTAGCGGGTGTG[C/G]GGCCCCGGAGCTCGG | 29979 |
rs559290918 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83670109 | GTGATGACAACTGTA[C/T]ATTTAGGCAAATTTT | 29979 |
rs559310239 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83701879 | AGTGTTCAGAGGCAT[C/T]AGTCACAATAGCCAG | 29979 |
rs559340383 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83703899 | AGGAAAATAAATTAC[C/T]ACCTTACAATTTACC | 29979 |
rs559378926 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83696820 | GTTCTTACAGTACTC[A/G]GGGGCAGGGGGGCTG | 29979 |
rs559394089 | snp | A/C | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83700476 | TAACACAATGGTGAA[A/C]AATCACAGCCCCTCT | 29979 |
rs559406813 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83698131 | ATCATGCCTTATAAA[A/T]CATGCCTGCAATAAA | 29979 |
rs559447667 | snp | A/C/T | 6.59591e-05 | 0.00574246 | synonymous-codon | UBQLN1 | GRCh38.p7 | 9:83678597 | CCTGGCAAGTTCCAA[A/C/T]GTCTACGAAAAATAT | 29979 |
rs559816850 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83688091 | TTTCCCTTTAGTACC[C/T]ATCCGAAATAGTAAT | 29979 |
rs559908949 | snp | A/G | 0.00159617 | 0.0282053 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83708008 | CGGAGCACGCCGGGT[A/G]ACGCGCCTGGCGGCG | 29979 |
rs559960752 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83666054 | GAAGCACTTCAAAGT[C/T]AGTACAATGAAAGGA | 29979 |
rs560055954 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83681782 | CAAAGGACTACAAGA[A/G]ATGATATATGCCACT | 29979 |
rs560074503 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83665421 | AAGCCACAACTATTC[C/G]CCTTCTCCAACAGAA | 29979 |
rs560144199 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83674760 | ATACTGCTCAATTGT[A/G]TGGGGAGTCAATGGT | 29979 |
rs560241446 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83675767 | GAGTACGTATTTTGA[A/G]TAAGTCAGTCAAGTC | 29979 |
rs560263013 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83696828 | AGTACTCGGGGGCAG[C/G]GGGGCTGGGTGAAGG | 29979 |
rs560304460 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83675841 | AAACAGAACACTGAA[C/T]CCCAATTATGCAAAA | 29979 |
rs560307643 | snp | C/T | | | utr-variant-3-prime | UBQLN1 | GRCh38.p7 | 9:83661395 | TCACAATAAGCAATA[C/T]TGTACCACAAATTAT | 29979 |
rs560395364 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83702484 | TGGATAAGATGTTGT[C/T]CAGCAGAAATATATA | 29979 |
rs560398834 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83662387 | CTGGTATCCTCATGT[A/G]TAAAATTCTAAAGCT | 29979 |
rs560424226 | snp | C/T | 3.40124e-05 | 0.00412372 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83679732 | ATTAAATAACAAATA[C/T]ATCATTTTTTAGCTA | 29979 |
rs560461927 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, synonymous-codon | UBQLN1 | GRCh38.p7 | 9:83668608 | AGCCAGCATTAAGAT[C/T]CCCAATTTTCTTAGC | 29979 |
rs560493096 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83683616 | TGAGTATAATGTACA[C/T]AAATATTTCATTAGT | 29979 |
rs560510362 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83689861 | GAAAAATGGCCAAGA[A/G]ATTGAAACAGGAATT | 29979 |
rs560570864 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83677333 | TTTGGGAGGCCAAGG[C/T]AGGCGGATCACCTGA | 29979 |
rs560589831 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83702057 | TAAGTGAAAGCCAAT[C/T]ACAAAAGACCACATG | 29979 |
rs560633798 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83683402 | CCTGGGCAACAGAGC[A/G]AGACTCCGTCTCAAA | 29979 |
rs560653148 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83696265 | GTGACTAAATCAAGC[A/T]AATATATCTATCACC | 29979 |
rs560669649 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime | UBQLN1 | GRCh38.p7 | 9:83660409 | AAATGTATCACTGAC[C/T]CTCAATTATGTTTTA | 29979 |
rs560696489 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83676710 | TTAAAAATTCTTCAT[C/T]CAGCACCTCATCTTT | 29979 |
rs560739658 | snp | A/G | | | upstream-variant-2KB, intron-variant | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83709015 | AATCAATGTTGCACA[A/G]TTTAAATCCTGACAG | 29979 |
rs560773838 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83704586 | AATCCTAGCACTTTG[A/G]GAAGCCGAGGCAGGC | 29979 |
rs560900689 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | UBQLN1 | GRCh38.p7 | 9:83667018 | AAAATCAGTCAGGCC[C/T]AGCACCAACAGTCCT | 29979 |
rs560904270 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83693012 | ACTCAAAATGAAAGA[C/T]ACATGATAGAACGGG | 29979 |
rs560981203 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83698684 | TTTTGGGAGACCAAG[A/G]GGGCAGATCGCTTGA | 29979 |
rs560987029 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | UBQLN1 | GRCh38.p7 | 9:83667700 | CATGTCATCTTAAAC[A/G]TATCCTTTCACAGAT | 29979 |
rs561025371 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83685871 | TAAAAAAATTGTTAT[C/T]GACAGCAAGGAAAGA | 29979 |
rs561053860 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83705174 | CAACAGGAACTCCCA[C/T]GTATCTTCATTGGCG | 29979 |
rs561114185 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83706271 | AATCGATTATAATAC[A/C]GTAAAATGCTAATTG | 29979 |
rs561282612 | snp | C/T | 0.000103243 | 0.00718406 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83669369 | TATTAAGGAAAAATA[C/T]TTAAACAAAAGTTAA | 29979 |
rs561297293 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83669850 | TAACATTTGAAACCA[C/T]AGAGCACAGTGACTC | 29979 |
rs561542680 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83697655 | CTGCCTCGCAGATTC[A/T]AGAGATTCTTCCACC | 29979 |
rs561579773 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83706817 | ACCCAATGATTGGCA[G/T]CTAAGAGATGATAAA | 29979 |
rs561639583 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83700709 | GCAAGAACAAACTGT[A/G]CAGAAGTCCTCAGGC | 29979 |
rs561672937 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83673059 | ACATGGCGAAACCCC[A/G]TCTCCACTAAAGATA | 29979 |
rs561714619 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83678083 | CTGGAGTGCAGTGGC[A/G]CGATCTCGGCTCACT | 29979 |
rs561716022 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant, nc-transcript-variant | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83708398 | CCCTCCCTTGCCTCT[A/C]TGTCTACTCTGCGTT | 29979 |
rs561753250 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83682571 | CCAGACCCCCTTCCA[C/T]GTGTTCAGGACAGTT | 29979 |
rs561761214 | snp | C/G | 0 | 0 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83662995 | GTGGGAGGATTGCTG[C/G]AGCCCAGGAGGTGCA | 29979 |
rs561805740 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83709026 | CACAATTTAAATCCT[A/G]ACAGCCCACTATGAC | 29979 |
rs561815610 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83663737 | TTTCTTACTCAATAT[A/C]CTTAAGACTGTATTT | 29979 |
rs561919491 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83703546 | AAAAGAAAATCCAAA[A/G]TCCCAAACACTTCTG | 29979 |
rs561921597 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83683949 | CTACTTGAACCCAGG[A/C]GGCGGAGGTTGTAGT | 29979 |
rs561933093 | in-del | -/AT | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83696898 | AATCAATGATCTGAC[-/AT]AGACTGATGAGTCCA | 29979 |
rs562175709 | in-del | -/GTCT | 0.00199481 | 0.0315187 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83686965 | CACTTCTGGTCCCAA[-/GTCT]GTCTGTTTAAAAAAA | 29979 |
rs562216201 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83671801 | ACACATTAGCCCCAA[A/C]AGTCAGCCTTTCCTT | 29979 |
rs562234941 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83683733 | TATATAAAAAACTTT[C/T]TTATCTTGGCCAGGT | 29979 |
rs562306841 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83665240 | CTTCTGGAGAAAATC[C/T]AAAACCTTACTCCTG | 29979 |
rs562380204 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83671264 | CTCCTGTTCATGTTG[A/G]TATTTTGACATCCTC | 29979 |
rs562401198 | in-del | -/A | 0.35196 | 0.228263 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83675469 | ACTTCCTATGCCGTC[-/A]AAAAAAAAAAAAAAT | 29979 |
rs562404562 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83693939 | GAATTAAGAGACATA[C/T]GGAAATTTCCTGGGC | 29979 |
rs562419877 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83678317 | TGAGCCACTGCACCC[A/G]GCCACTGAACTTTTT | 29979 |
rs562434352 | snp | C/T | 0.00636936 | 0.0560724 | upstream-variant-2KB, intron-variant | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83709908 | CCGCAATTATTTATG[C/T]ATCAACCTAATATTT | 29979 |
rs562442743 | snp | A/G/T | | | intron-variant, utr-variant-3-prime | UBQLN1 | GRCh38.p7 | 9:83667520 | ACCTTTCAGGAACAT[A/G/T]CAGTATTTATTTCAA | 29979 |
rs562531397 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83680952 | AAATGAAGCTGAATC[C/T]TGGACACAGAGCTGG | 29979 |
rs562626317 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83674578 | TTAATTAAATCTTGA[C/T]TGCAGTAACCAAATG | 29979 |
rs562731713 | snp | A/T | | | upstream-variant-2KB, intron-variant | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83709770 | GCACTTTTTAGATAT[A/T]ATCCTGACCTGCATG | 29979 |
rs562744038 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83680970 | GACACAGAGCTGGTA[C/T]TGGACAATTGGCTGG | 29979 |
rs562832766 | in-del | -/GG | 0.0158469 | 0.0875917 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83704585 | TAATCCTAGCACTTT[-/GG]GAAGCCGAGGCAGGC | 29979 |
rs562868186 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83664742 | TCCATCTCTAAAAAC[A/C]GTAACAACAACAAAT | 29979 |
rs562880337 | snp | A/G | | | utr-variant-3-prime | UBQLN1 | GRCh38.p7 | 9:83661038 | TGTGAATGAATGTTG[A/G]GACAATGTTACATTA | 29979 |
rs562925915 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83689461 | TAACATATGACCTAA[C/T]TGAGCATACACAGAT | 29979 |
rs562973234 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83707446 | GTCTCCTGGGGCGGC[A/G]GGCGGAGGTCCTGCC | 29979 |
rs562979557 | snp | A/C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | UBQLN1 | GRCh38.p7 | 9:83661518 | TGCAGGACAAAATCT[A/C/G]GTCACCCAACTATAA | 29979 |
rs563087543 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83682467 | CTCCGTGACTGAGCA[A/T]GATCCTGCCTCTCTT | 29979 |
rs563136066 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83696025 | GCTCACTGCAACCTC[C/T]ACCTCCCGGATTCAA | 29979 |
rs563172511 | snp | A/G | 0.00195167 | 0.0311773 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83678619 | GAAAAATATTTCCAA[A/G]AAAAGAAAAAAAAAA | 29979 |
rs563220371 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83688791 | GCTTGAACCTGGGAG[G/T]CAGAGGTTGCAGTGA | 29979 |
rs563268554 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83704550 | TCGTACTGGGCCGGG[C/T]GCCCGGTGGTTCACA | 29979 |
rs563268630 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83698164 | TTGGCCATTATGTCA[C/T]TGTCATTAACAGCAT | 29979 |
rs563287897 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83691907 | GTTCTAGGGAACTAC[A/G]GACAACTGCATATGA | 29979 |
rs563313175 | in-del | -/TTTTT | 0.00159681 | 0.0282109 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83671671 | TCCAGGCTTTTTTTC[-/TTTTT]TTCTTTTTTTTCCTG | 29979 |
rs563322258 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83685162 | AATAGAAGGAATATG[C/T]TGAATGAGTAAAGCA | 29979 |
rs563404890 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83704003 | GTTAAGGAATCTACA[C/T]TACATAGAAATACTT | 29979 |
rs563482233 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83692897 | AATATTTTCATCTAG[C/G]GAATAGCCAGAACCA | 29979 |
rs563532130 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83698641 | ATTCTGGCTGGGTGC[A/G]GTGGCTCACACTTGT | 29979 |
rs563543197 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83685784 | GTATAATAACTAAAT[A/G]CCAATGAACCTTGTA | 29979 |
rs563556229 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83669864 | ATAGAGCACAGTGAC[C/T]CCAAGCAGTATCAGG | 29979 |
rs563574143 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83666235 | GAATTGACAGCATTA[C/T]TGGTCTCTATTCTAT | 29979 |
rs563613384 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83705408 | GTGCCTGCCACCACG[C/G]CCAGCTAAGTTTTGT | 29979 |
rs563782758 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83676547 | AGAATATTTTTATTG[A/T]TTTAAAAATGGTATT | 29979 |
rs563858251 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83682445 | GATGGCATCACTGCA[C/T]TCTAGCCTCCGTGAC | 29979 |
rs563871749 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | UBQLN1 | GRCh38.p7 | 9:83660019 | ATAAATTGTCAAATT[A/G]GTTATGACACTATCC | 29979 |
rs563987641 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83666867 | CTCAACACACAAGTG[A/G]CAGGCACAGAGAAAA | 29979 |
rs564046316 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83674837 | GAACAACCAGGGTAA[C/G]ACCATTTTTTAAAAA | 29979 |
rs564046840 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83706162 | GTTGAACTTAGGCAA[A/G]TAAGTTCACAATGCT | 29979 |
rs564071763 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83702147 | GTTGCCTAAGGCTGG[C/G]GGGCCCAGGGAGAAA | 29979 |
rs564096010 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83662946 | CCAGGTGTGGTGGTC[C/T]GCGCCTGTAATCCCA | 29979 |
rs564247804 | in-del | -/TT/TTT | 0.41141 | 0.19091 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83705246 | TGAAGCCAGCACTCC[-/TT/TTT]TTTTTTTTTTTGAAA | 29979 |
rs564316654 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83681100 | AGTTTTATTAACAGG[A/G]AGCAGAATTCACCTA | 29979 |
rs564347452 | snp | A/G | 0.00119737 | 0.0244387 | downstream-variant-500B | UBQLN1 | GRCh38.p7 | 9:83659720 | TAAAGAAACCATGAC[A/G]CCTCAATGTCACATA | 29979 |
rs564445227 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83697604 | TCTGTCGCCCAGGCT[A/G]GACTGCAGTGGCAAG | 29979 |
rs564455407 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83683172 | AATCCCAGCACTTTG[C/G]GAGGCCGAAGCTGGC | 29979 |
rs564564313 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83696907 | TCTGACATAGACTGA[G/T]GAGTCCAATTACCCT | 29979 |
rs564569243 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83671200 | TCCTCCATAGAAGTC[C/T]TGAACCCCTCAAAGG | 29979 |
rs564623804 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83689919 | AATGGCAAACAACAC[A/T]GGTAACTTTAAATTA | 29979 |
rs564628159 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83678075 | GACCCAGGCTGGAGT[A/G]CAGTGGCGCGATCTC | 29979 |
rs564907632 | snp | C/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83692092 | GAAATAAGCAACTTT[C/G]TAAGTTTAGCTGTCT | 29979 |
rs564915769 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83686602 | CTTTTTATGTTAATG[A/C]GACCAAATTTAGTTC | 29979 |
rs564942878 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | UBQLN1 | GRCh38.p7 | 9:83661462 | TTCTACATAAATTAC[C/T]ACCATAGGCTAATGT | 29979 |
rs564976500 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | UBQLN1 | GRCh38.p7 | 9:83667126 | TCACCTCACTACTAC[C/T]AGAGATGAGAAAAGT | 29979 |
rs565133869 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83673739 | TATGGGTGTTTTGCA[C/T]TTTTACAAAAGCAGT | 29979 |
rs565362453 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | UBQLN1 | GRCh38.p7 | 9:83667738 | TTATTAGATACTTCT[C/T]ATAACTTACCTGAGT | 29979 |
rs565382224 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83688682 | CTTGGCCAACATGGT[A/G]AAACCCCGTCTCTAC | 29979 |
rs565393424 | in-del | -/TT | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83683599 | CAATTGCCCCTCCTC[-/TT]TGAGTATAATGTACA | 29979 |
rs565396402 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83694803 | GTACTTTATGCATAC[A/G]ATGTCACAAAATCCT | 29979 |
rs565412216 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83706884 | AAAGTCATTCACTTT[C/T]CTCCTTAAACCTAGT | 29979 |
rs565423822 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83663011 | AGCCCAGGAGGTGCA[C/G]GTCGCAGTGAGCTGT | 29979 |
rs565518396 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83683748 | TTTATCTTGGCCAGG[C/T]GCGGTGGCTCACGCC | 29979 |
rs565529995 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83697194 | ACAGTCTACTACTTA[A/G]TATGTGTATGAATTT | 29979 |
rs565602439 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83665350 | TTACTTGACCTCCTC[C/T]TAAGTCCATCATGAA | 29979 |
rs565653573 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83690735 | TGGTCAATGGAACCA[A/G]ACTCTGTCTCAAAAA | 29979 |
rs565667580 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83702973 | TAAATGTACTTCAAA[A/C]TTTTACACATAACCT | 29979 |
rs565734368 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83702312 | CACTTCAATTACGCT[C/G]TTTCTTAAAAAAAGC | 29979 |
rs565743616 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83703730 | AGTGCTCCGTGAATA[A/G]TAAATTTCACTCTAA | 29979 |
rs565746285 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83708481 | TTTAATATGCTTAGC[G/T]TTTGATATTTGGAGG | 29979 |
rs565769559 | snp | C/T | 0.0287284 | 0.116357 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83677526 | GAGATCGTGCCATTG[C/T]ACTCCAGCCTGTGCA | 29979 |
rs565800259 | snp | C/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83692278 | ATTCTGCACGTACTT[C/G]AAATATCTTTTACTT | 29979 |
rs565883022 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83709437 | TGTCTTACCTGCATG[C/T]TTTGCCTAGGCTGCC | 29979 |
rs566137244 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83691559 | ATGTCCTAGATGCAG[C/T]AGAGTAGGACACTAC | 29979 |
rs566255410 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83698749 | TGAAACCCTGTCTCT[A/G]CAAAAAAATACAAAG | 29979 |
rs566277822 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83698424 | TATATTTCAAAGACT[A/T]AGTATTTCAAAATGC | 29979 |
rs566348115 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83706552 | TTCAGGAATTGTTGT[C/T]TCCTGTCACCAACTG | 29979 |
rs566541911 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83701570 | AGTTTTCCTCAGAGT[A/G]CCCCCAGCAAAAATA | 29979 |
rs566584369 | snp | A/C | 0.0166325 | 0.0896639 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83673560 | TTAAAAAAAAAAAAA[A/C]AAAAAAACAAAAAAA | 29979 |
rs566622902 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83688973 | GTAATTCACTCATTT[-/A]AAAGTATACGATTCA | 29979 |
rs566662617 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83694923 | GATTTCTCCAATTCT[A/C]AGGTTCATGCTCTCC | 29979 |
rs566727371 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83707079 | AGGATCCCACCCACC[C/T]CTTTTTAATTCATGA | 29979 |
rs566772760 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83662768 | ACCCTACCCTATTTA[C/T]TATATTTAGTAAGGC | 29979 |
rs566789808 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83700961 | CTGGTGGGAGAGTTA[C/T]AGAAGTCAGGCAACT | 29979 |
rs566843944 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83668890 | AGTTTATCTTCAAAA[A/G]AGTGGGCATTCCAGA | 29979 |
rs566925751 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83687780 | GCCAATATAAACAAC[C/T]GATTTTTAAAAAATC | 29979 |
rs566925758 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83695618 | AGAGAGCTTTAAAGA[A/G]TTAAAAAAAAAAATT | 29979 |
rs566987053 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83688340 | TAAACTGGTAGTTAG[G/T]ATTCAAACTTAGATT | 29979 |
rs567056663 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83679017 | TGAGCCACCGCGCCC[A/G]GCCAGGAGGCCACTG | 29979 |
rs567073070 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83708210 | GCAGTTTCCAGTTAA[G/T]CGCTGTAACGGCGCA | 29979 |
rs567085222 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83672185 | TGTGGCTGGTGTGAT[C/T]GTCTATCCAGATCAC | 29979 |
rs567144028 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83681873 | CAAATGGTAGAGCTA[C/T]AATACAGCAGAATGA | 29979 |
rs567181148 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83710150 | TGAATGGTTTTTGTT[G/T]GTTAAATGGTCTGTC | 29979 |
rs567246977 | snp | C/T | 0.000799041 | 0.019972 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83671670 | ATCCAGGCTTTTTTT[C/T]TTTTTTTCTTTTTTT | 29979 |
rs567292741 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83685215 | CAGCATAAAAACTTA[C/T]AGGAGTGTTAATGGC | 29979 |
rs567323042 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83690963 | GCCAACATGGCAAAA[C/T]CCCGTCTCTGCTAAA | 29979 |
rs567332806 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83687277 | AGACACATAAAACCA[A/G]ACAAGAGAAAAGAGC | 29979 |
rs567443168 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83668703 | CAGCAGGGGAATCAA[C/T]AGTTGAAAGAAGGAG | 29979 |
rs567497977 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83686765 | TCTCTAATGCAAATA[A/C]CCCAAATATGAAATG | 29979 |
rs567572692 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83693434 | CTGTCCAGACTCTCA[A/C]GGTATCTTGTATCTG | 29979 |
rs567622066 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83704822 | TGACAGAGACTCCAT[C/T]TCAAAAAAAAAAAAA | 29979 |
rs567685101 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83698921 | CTGTCTCAAAAAAAA[A/G]AAAAAAAGTAAATTC | 29979 |
rs567777416 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83705453 | CGGGGTTTCACCCCG[C/T]TGGCCAGGCTGGTCT | 29979 |
rs567883649 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83680181 | CAAATCGAATACCTA[C/T]TACTAATATTTAATT | 29979 |
rs567890514 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83690006 | GAGGATGCAGAGCAA[A/C]TGGAAACCACACACA | 29979 |
rs567964420 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83696426 | GCCTGTCTGGGCAAC[A/G]TGGCAAAATCCTGTC | 29979 |
rs568029429 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83697077 | CACCACACCTAGCTA[C/T]TCAATGAACTTTAAA | 29979 |
rs568091549 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83708115 | GTGCAGGCGAAGCCA[A/G]TGTGAAGGACTAAAA | 29979 |
rs568112690 | snp | A/C | 0.00119737 | 0.0244387 | utr-variant-5-prime, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83707796 | GAATGCAGAGCACGC[A/C]GCCTCAGTAGCAACG | 29979 |
rs568134259 | in-del | -/CTT | 0.00159617 | 0.0282053 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83689191 | GGTCTTTGTGACTAG[-/CTT]CTTATACTTGGCATG | 29979 |
rs568161404 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83662035 | CTTTTTTATAACATA[C/T]GCTGATCTACTGAGC | 29979 |
rs568162921 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83673714 | GGAACAGTCATTCTC[A/G]CTTATTGTCTATGGG | 29979 |
rs568199862 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83683192 | CCGAAGCTGGCTGAT[C/T]ACGAGGTCAAGAGAT | 29979 |
rs568306444 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83692637 | GCAGGCGGATCACCT[A/G]AGGTCGGCAGTTTGA | 29979 |
rs568355844 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83689141 | CTTTCTGTTTCCATA[C/T]GAGTATTTCATATAA | 29979 |
rs568429411 | snp | C/T | 0.0287284 | 0.116357 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83677518 | GGTGAGCTGAGATCG[C/T]GCCATTGTACTCCAG | 29979 |
rs568447750 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83708721 | TGCTACGATGACAGC[C/T]GTGCGCGAGCGCCCC | 29979 |
rs568469907 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83663341 | TAAAACCAATGTATG[C/T]TTGTAGATGCAACCA | 29979 |
rs568493022 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83670868 | CTCTATCTCAAGAAA[C/T]CACTCTTTGCTCATC | 29979 |
rs568627166 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83704126 | TCTGACCCTCCAAAA[C/T]TAGGTACAAATTTTA | 29979 |
rs568686648 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83703672 | TCTCACTACCTATTC[C/T]AGCAACCTGTAAGTA | 29979 |
rs568860165 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83673003 | TTGGGACGCTGAGGC[G/T]GGTGGATCATTTTAG | 29979 |
rs568966922 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83706984 | GGTGGGAAAGATTTC[A/T]GGAGTTAAAATGCAG | 29979 |
rs568998289 | in-del | -/AA | 0.470811 | 0.117228 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83663070 | AAGGGAAAGGGAAAG[-/AA]AAAAAAAAAAAAGGG | 29979 |
rs569001336 | snp | A/C | 0.00119737 | 0.0244387 | utr-variant-3-prime | UBQLN1 | GRCh38.p7 | 9:83660894 | GTGAAAGCAACATTT[A/C]AATTACAAATTTTAA | 29979 |
rs569063610 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83700123 | ATATTCATTATGAAC[C/G]ATCTTTGAAAAGAAA | 29979 |
rs569097904 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83674958 | ACTTAGTTGGACATA[C/T]TTTCAAAGCATATAA | 29979 |
rs569136816 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83668812 | AGTGATCTACTAAAT[A/G]AAAGTATTTCAAATG | 29979 |
rs569160525 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83706431 | GGTAAAAGTTTCTCT[C/T]ATTTGATGTTACACA | 29979 |
rs569245842 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83663731 | GCCTGTTTTCTTACT[C/T]AATATCCTTAAGACT | 29979 |
rs569301605 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83665740 | AGTCATTTGCATAAT[A/G]CATGAGGCCCTAGAA | 29979 |
rs569347086 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83700862 | TACTCCATTATATAT[C/T]CTAAGACCAACAGGG | 29979 |
rs569348285 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83694283 | TAGTTATCTGAATAC[C/T]GTATTCAAATCTTTG | 29979 |
rs569452119 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83682016 | AATAAGCCACTGAGT[C/T]TGGCTATCTATTATC | 29979 |
rs569457776 | in-del | -/AAAC | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83684020 | AGAGAGACTCTTGAA[-/AAAC]AAACAAACAAACAAA | 29979 |
rs569497216 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83681335 | TTTTTATATATGCCA[G/T]AGACTGTGTTACATA | 29979 |
rs569506244 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83678171 | GGACTACAGGCGCCC[A/G]CCACCACGCCCAGCT | 29979 |
rs569617285 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83677593 | AACAAAACAAAAGCA[A/G]CATGAAAAATATAGT | 29979 |
rs569626321 | snp | C/G | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83709733 | CCTGTAAGAAGATAC[C/G]ATATAGTTATCCATT | 29979 |
rs569715606 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83683381 | GCGCCACTGCACTCC[A/G]TCCAGCCTGGGCAAC | 29979 |
rs569725889 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83704783 | GTGAGCCGACACCAT[A/G]CCATTGCACTCCAGC | 29979 |
rs569742132 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83703620 | AAAAATCTCTATTAA[C/T]GACAGCACCTTGGAA | 29979 |
rs569802938 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83697717 | TGCACCACCACACGC[A/G]GCTATTTTTTGTACC | 29979 |
rs569811202 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83683751 | ATCTTGGCCAGGTGC[A/G]GTGGCTCACGCCTGT | 29979 |
rs569877103 | snp | A/C | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83690316 | CACGAGCGAAAAAGC[A/C]AGTCACAAATGAATA | 29979 |
rs569890272 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83691346 | AAAGATGATCCATTA[A/T]CATCGTATGTGGCAG | 29979 |
rs569900738 | snp | A/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83687294 | CAAGAGAAAAGAGCA[A/T]CATGCTATAAAGAAA | 29979 |
rs569955030 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83684393 | AGAGACAGCGTTTCA[C/T]CATGTTTACCACGCT | 29979 |
rs569986838 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83698809 | TCCCAGCTACTTGGG[A/G]GGCTAAGGCAGGAGG | 29979 |
rs570009170 | snp | A/C/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83693130 | AAGCTGAGAATTACT[A/C/G]AACTCTTTCTCAACA | 29979 |
rs570228174 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83693336 | CCAAAATTGTTTTCC[A/T]TTCTACTGAATGTAA | 29979 |
rs570261725 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83707110 | AACAAAACCGCAGCC[C/T]GAGCTAAAGCGAACC | 29979 |
rs570384182 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83701667 | ATCACAAAGACAGTA[A/G]TAAGTATTACCGAGA | 29979 |
rs570550485 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83696303 | TCTTTTTTGTAGTTG[C/T]AGCTGCTGGTACAGG | 29979 |
rs570622426 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83688534 | TATATAGCATTTTAT[C/T]GTATTTTAGGATTTG | 29979 |
rs570815205 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83688983 | TCATTTAAAGTATAC[A/G]ATTCAATGGTTTCTG | 29979 |
rs570826087 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83678963 | CCTGACCTCGTGATC[A/C]GCCCACCTCAGCTTC | 29979 |
rs570856219 | snp | A/G | 7.0242e-05 | 0.00592588 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83669333 | AACATACTAGCTGAA[A/G]GTTTGTTTTTAAAAA | 29979 |
rs570911152 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83663168 | GGGGAAGAGGAAGGA[A/G]GAAAAGGAAAGGGGA | 29979 |
rs570924454 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83682152 | TAGCCGGGCGTAGTG[A/G]CACACTCCTATAATC | 29979 |
rs570949562 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83707131 | AAAGCGAACCCTCGC[C/T]CCCGCCCAGCCTCCA | 29979 |
rs571032077 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83709178 | GAATCCTGAGGGTAT[C/T]GATTTCAGTATAGAC | 29979 |
rs571066705 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83703047 | AGAAACTCCCCTCCA[C/T]TATCTGCACTAATGT | 29979 |
rs571074944 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83670217 | ATTCTCAAACTTACT[A/G]TGCCAAGTCAACTCA | 29979 |
rs571088185 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83703678 | TACCTATTCTAGCAA[C/T]CTGTAAGTAAAAATT | 29979 |
rs571134344 | snp | C/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83682367 | GCTCTCATCTGTAAC[C/G]CAGCATTTTGGGACA | 29979 |
rs571141714 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83662808 | GAAAGCAGGCCAGGC[A/T]CACGCCTGTAATCCC | 29979 |
rs571164385 | snp | C/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83665306 | ACGCAAGTATCTCCT[C/G]TTTGACAGCAAACCT | 29979 |
rs571219573 | snp | A/C | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83682345 | CTAATACAGGCCAGG[A/C]ACAGTGGCTCTCATC | 29979 |
rs571276839 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83692476 | ACTTAATTAGCCATC[C/T]TAGAAAATCTCAAAG | 29979 |
rs571285330 | snp | A/C | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83684631 | AGCCTGGCCAACATG[A/C]GGAAACCCCGTCTCT | 29979 |
rs571297224 | snp | C/T | 0 | 0 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83679027 | CGCCCGGCCAGGAGG[C/T]CACTGTTTTGGACCA | 29979 |
rs571390295 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime | UBQLN1 | GRCh38.p7 | 9:83660119 | AAAGACACATGAATA[C/T]CCTTCTTAACAATCT | 29979 |
rs571475173 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83705506 | CCTCGGCCTCACAAA[C/G]TGCTGGGATTACAGG | 29979 |
rs571537577 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83672798 | TCACTGCAAACCTTC[A/T]AACTGTGAAAATCAC | 29979 |
rs571609620 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83694189 | AAGTAAAATTTACTT[C/T]AGCTCTGAAGATAAA | 29979 |
rs571626513 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83687436 | GACTGGCTCAAGAAA[C/T]CAGTCCAAATTCAGA | 29979 |
rs571684564 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83693507 | TTCTTGTCTTGAAAG[C/T]ATACCTTCTTTCTCC | 29979 |
rs571701936 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83689197 | TGTGACTAGCTTCTT[A/C]TACTTGGCATGTTTA | 29979 |
rs571841464 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83674335 | TTATGCAATGACACT[A/G]AAAGAATACAACATA | 29979 |
rs571933319 | snp | A/C | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant, nc-transcript-variant | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83708342 | TTACCTCATGCCCAG[A/C]TGGGCCGTGTTCACC | 29979 |
rs572193396 | in-del | -/A | 0.00438332 | 0.0466095 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83687652 | AGGGAAGGCATATAT[-/A]AAAAAACATGATAAG | 29979 |
rs572237551 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83670380 | TTGTAAATTTTAACT[C/T]AGTTTTTTTTTCACA | 29979 |
rs572258623 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83676474 | TTTAAAGTAAGAACA[C/T]TGCAACCCTCTCAAA | 29979 |
rs572273656 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83675465 | ACAGACTTCCTATGC[A/C]GTCAAAAAAAAAAAA | 29979 |
rs572304984 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83662931 | AAATACAAAAATTAG[A/C]CAGGTGTGGTGGTCT | 29979 |
rs572356090 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83697531 | CACTCCAGCCGGGGC[A/G]ACAGTGCAAGACACT | 29979 |
rs572485374 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83702491 | GATGTTGTCCAGCAG[A/G]AATATATATAAGCCA | 29979 |
rs572491302 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83703106 | GATGTTATCTTGCTC[A/G]TGGATACTTGGAAAT | 29979 |
rs572592519 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83663441 | AGGAGGTGGTGTCAT[A/G]GGTGGAGTTAAGGTA | 29979 |
rs572670679 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83697847 | TTCAAGCGATTCTCC[C/T]GCCTCAGCCTTCCGA | 29979 |
rs572671502 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83683828 | GGAGTTCAAGACCAG[C/T]CTGGCCAACATGGTA | 29979 |
rs572746199 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83690366 | TATGTGAGTTTTTTC[A/G]TTTTTTTAAGGGTTG | 29979 |
rs572809466 | snp | A/C/T | 0.00199481 | 0.0315187 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83683448 | AAAAGAACCACTGAA[A/C/T]TCCTGACATCTAGAA | 29979 |
rs572835614 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83705224 | GCATTTTTCAGTATA[C/T]GTGCTGCTGAAGCCA | 29979 |
rs572907538 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83696854 | GAAGGAGACAATCCA[C/T]ATAATCACAAAATAT | 29979 |
rs573020389 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83700277 | CAAGAGTTGTGCCTG[A/G]AGAGTGGTGACCTGG | 29979 |
rs573058249 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83662157 | AATCATGTCAAATAG[A/T]TCACGACTCTACTTT | 29979 |
rs573067984 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83687130 | TGAGCAGTCCAATGA[C/G]AGTCAAGTAAAACCA | 29979 |
rs573142706 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83693686 | CCAATCTCAGCTGCT[A/G]AGGGCTGACTTTGCT | 29979 |
rs573220892 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | UBQLN1 | GRCh38.p7 | 9:83661419 | AAATTATAGAGTGCA[A/G]ATGATTTGCTTCTTT | 29979 |
rs573258586 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83680623 | AAACCTGGATGGAAC[C/T]TTTGAGCCCAACTTC | 29979 |
rs573391608 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83695129 | ATGAACATATAAATA[C/G]CTTTCTGGACAGAAT | 29979 |
rs573461912 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83664965 | AGGCAGAATAATACT[A/C]AATCTGAAATTCTCA | 29979 |
rs573504377 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83698045 | CTGGCCAGCATCTTC[A/T]TTTTTTAAAAAAAGG | 29979 |
rs573528226 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83701375 | CACACCTTAAAGACT[C/G]TAGCCAAGTGCACTG | 29979 |
rs573560789 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83707217 | GCGACGGAGGGCGGG[A/G]AACTGGGGGAGGAGG | 29979 |
rs573619867 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83680667 | CCCATACCTTGTGCC[C/T]TAATAATTATCTTCC | 29979 |
rs573625713 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83707830 | GCAGGGCCACCGTAG[C/T]GGGTGTGGGGCCCCG | 29979 |
rs573664703 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83677240 | CACAAGTAAATAAGT[A/G]TTCTCTCTACATTTA | 29979 |
rs573694677 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83683791 | ACTTTGCGAGGCCGA[A/G]GCAGGCGATCAACTG | 29979 |
rs573770972 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83701343 | ACAGCTGGATTTTCA[C/T]ATCTGTTGTCATATC | 29979 |
rs573824420 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83691820 | GGGTATCTTAGTCTT[C/G]AAGTATGAATTTATG | 29979 |
rs573942623 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83684966 | GGATCTGTCTTACAA[C/T]TGCTGACAGCCAGGC | 29979 |
rs574082004 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83695892 | CAGTCTCTAAAAAAA[A/G]CTCCTAATCTCAATT | 29979 |
rs574142068 | snp | G/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83690642 | GGGAGGCCAACATGG[G/T]AGGACTGCTTAAGCC | 29979 |
rs574142241 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83664508 | CTGTGTCCCAACTAC[G/T]GGGGAGGCTGAGGTG | 29979 |
rs574158027 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83701312 | TTTGGAAATCACTTT[A/C]GTCTTGTAATAGAAG | 29979 |
rs574203556 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83688151 | AGAATTAAACGAGAA[C/T]GTATATAAATGCAAA | 29979 |
rs574284217 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83678883 | CCACCACGCCCCGCT[A/G]ATTTTTTTTTGTATT | 29979 |
rs574649544 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83681705 | GATAGCAGTGCTCAC[C/T]AAACATTTCATTTTG | 29979 |
rs574670736 | in-del | -/TC | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83695845 | ATGCTAATCCAACAG[-/TC]TCTGCAAACAGCAGA | 29979 |
rs574702359 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83662843 | CTTTGGGAGGCCAAG[G/T]CGGGTGAGATCGCTT | 29979 |
rs574731594 | snp | A/C | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83693554 | TTAATCTGAGGAAGA[A/C]GCAGCAAATAATTAA | 29979 |
rs574731788 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83666652 | CTCTCAATGAGAATG[A/G]TGGTTATGATAATGA | 29979 |
rs574746770 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83702437 | CATTTTTTTTCTCAG[A/G]TATCTTGCTATACTG | 29979 |
rs574856541 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83707941 | GACATCCGCAGCAGC[C/T]ACCGCTTCCTCCTCC | 29979 |
rs574873997 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83708263 | GAAATTACTAGAAAG[G/T]GACCAGTGGGCCCTG | 29979 |
rs575039669 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83703076 | GTCTCACATATATAA[C/G]TCTCCATTCTTCTAG | 29979 |
rs575076557 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83690283 | AACTACTGCCACATA[C/T]CATCACGGATACCTC | 29979 |
rs575131365 | snp | A/C | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83674086 | TAACAAGTATGAGCC[A/C]CCATGCCACACCTGG | 29979 |
rs575153855 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83696668 | AAAAAATCCCAACTA[A/G]GTACAAAATATTGCA | 29979 |
rs575198287 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83705112 | CCCGCTAAAATAGCT[A/G]AAATTACAGAGACTG | 29979 |
rs575237616 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83697485 | TGAACCCAGGGGGCG[C/G]AGGTTGCAGTGAGCT | 29979 |
rs575334803 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83685851 | TAACATGGAATCACA[C/T]TTTTTAAAAAAATTG | 29979 |
rs575373751 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83671785 | TCAACTCAGTCACCA[A/G]ACACATTAGCCCCAA | 29979 |
rs575375648 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83678867 | GGACTACAGGCGCCC[A/G]CCACCACGCCCCGCT | 29979 |
rs575377843 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83679396 | TAAAGCTTTAAAGTT[A/G]TTGCAATTTTGTATT | 29979 |
rs575388180 | in-del | -/A | 0.459687 | 0.136129 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83674185 | AATCACTGCAGCATT[-/A]AAAAAAAAAAAAATA | 29979 |
rs575413282 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83672341 | CAAGAGGCCTAGCTT[C/T]TGGCCTATTTTAGCT | 29979 |
rs575413732 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83705701 | AACTAACTGCAAACA[C/G]CCCAGGTGACCTTCA | 29979 |
rs575434934 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83700598 | CCAATCCAGTCTGGA[A/C]AATCAGAAATAGATA | 29979 |
rs575462515 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | UBQLN1 | GRCh38.p7 | 9:83659637 | CATACCACTGCAGTA[A/G]CTTAAAGGTACTTCA | 29979 |
rs575474727 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83692943 | TGTAATTTCCATTAA[A/C]AAGATTACCTAGATT | 29979 |
rs575497210 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83673657 | TGAAACGTGAAAACT[A/G]TATGAAATTCAAATT | 29979 |
rs575533863 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | UBQLN1 | GRCh38.p7 | 9:83667633 | TCATCAACATATTAA[C/T]GAGGTTATCACACAT | 29979 |
rs575609454 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83676566 | AAAAATGGTATTACT[C/T]CAGGTTTTACAAAAC | 29979 |
rs575629812 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83683316 | ACTTGGGAGGCTGAG[A/G]CAGGAGAATGGCGTG | 29979 |
rs575636854 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83699571 | ATGATCACTGAGCCA[C/T]GGTGCTCAAGCAATC | 29979 |
rs575686337 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83686965 | CACTTCTGGTCCCAA[A/G]TCTGTCTGTTTAAAA | 29979 |
rs575705197 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83679494 | CATTCAAATAACATA[A/C]AGAAGGAAGCACTTT | 29979 |
rs575749894 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83707158 | TCCACCCCGCCCGGA[C/G]GCTGGCGGTGGGTCC | 29979 |
rs575835503 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83703288 | GAAATGCTCCAAAAT[C/T]TGAAATTTTTTAACA | 29979 |
rs575944236 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83673688 | TCAACGCCCATGAAT[A/G]CCATTTTATTGGAAC | 29979 |
rs576092411 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83697644 | CACTGCAACCTCTGC[C/T]TCGCAGATTCAAGAG | 29979 |
rs576138523 | in-del | -/A | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83685646 | AAGTTCCTTAGACTT[-/A]AAAGAAATATGATTA | 29979 |
rs576146668 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83663572 | GCAAAATCTATTTCA[A/T]ATGATTTTCAAATAG | 29979 |
rs576217179 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83664346 | ATTGCTTTAGCCCAG[A/G]AGGTAGAGGCTGAAG | 29979 |
rs576375231 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83672516 | ATAGGGAGACCCAAG[A/G]AGAGGAAGAGAGACA | 29979 |
rs576396664 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83690801 | ACAGCCAGCTCTCCT[C/T]AGTATTTCAATTTCA | 29979 |
rs576516886 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83706712 | AACCAAGTTTAAGTA[A/G]TATTCTGCATTCACT | 29979 |
rs576650056 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83691586 | CTACACCACACATTC[A/G]AAAATTACCTCCATT | 29979 |
rs576709505 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83684717 | TTGGGAGGCTGAGGC[A/G]GGAGAATCGCTTGAA | 29979 |
rs576712148 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83673356 | CCAGCCTGGCCAACA[C/T]GGTGAAACACTGTCT | 29979 |
rs576808930 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83705466 | CGTTGGCCAGGCTGG[C/T]CTCGAACCTCAGGCA | 29979 |
rs576817159 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83696181 | TTGACCTCATAATCC[A/G]CCTGCCATCATGATT | 29979 |
rs576846779 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83678077 | CCCAGGCTGGAGTGC[A/G]GTGGCGCGATCTCGG | 29979 |
rs577030778 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime | UBQLN1 | GRCh38.p7 | 9:83660360 | TACATGAGAGAATAT[A/C]ATCACCTAAGAGAAT | 29979 |
rs577037258 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83695030 | ATATGGAAAGACTAC[C/G]AAGGTAACACAAGTA | 29979 |
rs577091419 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83681514 | GCTACTTTCAGAAGA[A/G]GAGATAACACTTAAT | 29979 |
rs577098172 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83687858 | ATAACCAAAAAAGCA[A/T]AAAGATAACACAAAA | 29979 |
rs577249260 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83680789 | TGAACCTGAGGAGGA[A/G]GTCAGGGGAACCCCC | 29979 |
rs577269580 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83707366 | CGAACTTGGGTGTGA[C/T]CTAATTTGGGACGAC | 29979 |
rs577272583 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | UBQLN1 | GRCh38.p7 | 9:83668419 | AACTACAGATTATCA[A/C]GGTTTATTTCACATT | 29979 |
rs577332862 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83707865 | TCGGTGCAGGCTCTG[A/G]CGCAGGCCCGGGTCA | 29979 |
rs577380714 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83688690 | ACATGGTGAAACCCC[A/G]TCTCTACTAAAAATA | 29979 |
rs577412577 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83680375 | TTATTATTCATTACA[A/T]GCCCTTTTGATCATT | 29979 |
rs577420593 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83675220 | ATTGCATTATTTTAT[C/T]AGCTCATGCCAAAGA | 29979 |
rs577467630 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83705099 | ATATGGCTACACACC[C/T]GCTAAAATAGCTAAA | 29979 |
rs577515037 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83695989 | TCTGTTGCCAGGATA[C/G]AGTGCAGTCGCACGA | 29979 |
rs577597008 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83701954 | ATGTGGAATGCTGTT[A/G]GCAACACAATGGAAT | 29979 |
rs577632330 | snp | A/T | 1.99922e-05 | 0.0031616 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83678001 | ACAAAGAATAAGCTT[A/T]TGTTTTAAATAAGAT | 29979 |
rs577660198 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83702409 | GCAAATAAGAAAACA[A/G]TGATCTCACAGACAT | 29979 |
rs577669310 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83671192 | CAGTCCCCTCCTCCA[C/T]AGAAGTCTTGAACCC | 29979 |
rs577749596 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83685770 | TGCAAATAATTTAGG[G/T]ATAATAACTAAATAC | 29979 |
rs577818682 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83678246 | CAGGATGGTCTTGAT[C/T]TCCTGACCTCGGGAT | 29979 |
rs577819545 | in-del | -/T | 0.00398564 | 0.0444627 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83678189 | ACCACGCCCAGCTAA[-/T]TTTTTGTATTTTTAG | 29979 |
rs577840209 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83705997 | ATGACTGGGAAAAGG[C/T]AAGAAAAAACTTTCT | 29979 |
rs577883233 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83679344 | ATTTTATAAAATGAG[A/G]TGTTGTCTGATTCTA | 29979 |
rs577902070 | in-del | -/A | 0.00199481 | 0.0315187 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83698750 | AAACCCTGTCTCTAC[-/A]AAAAAAATACAAAGT | 29979 |
rs577911497 | snp | C/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83690101 | GCTTACCCTATGACC[C/G]AACAATTCCACTATT | 29979 |
rs577948558 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83697972 | AACTCCTGACCTCAT[A/G]TGATCCACCCGCCTC | 29979 |
rs577985700 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83704508 | AAAGGCTACTTCAGA[A/C]AGACTTTAATTTTAT | 29979 |
rs577991718 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83674161 | AATCAGTTATACTCA[C/T]GCAGCACAAAATCAC | 29979 |
rs578024522 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83692864 | TTTTAAAAATAATAA[C/T]AACAACAATAATAAA | 29979 |
rs578116730 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83666857 | GCTTAGAAACCTCAA[C/T]ACACAAGTGGCAGGC | 29979 |
rs578131254 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | UBQLN1 | GRCh38.p7 | 9:83667519 | AACCTTTCAGGAACA[C/T]ACAGTATTTATTTCA | 29979 |
rs578201279 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83673162 | TTGAACCCAGGAGAA[G/T]AAGGTTGCAGTGACT | 29979 |
rs578232235 | snp | A/G | 0.00119737 | 0.0244387 | downstream-variant-500B | UBQLN1 | GRCh38.p7 | 9:83659825 | ACAAAAGACTGTGAC[A/G]TTTTAATTGGAAAAC | 29979 |
rs745331323 | in-del | -/AGATAAG | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83684863 | CTTCCAGATGATACC[-/AGATAAG]AGATAAGAGTTTTGA | 29979 |
rs745335235 | in-del | -/GGTTGCTAGTAGCAGAACCAGATGTAGAGTTACTATT | 1.68207e-05 | 0.00290001 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83680042 | CCAAGGCCACCTAAG[lengthTooLong]AGGATAAAGGGCAAA | 29979 |
rs745403173 | snp | C/G | 3.32685e-05 | 0.00407837 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83678432 | TGAACCTTGGAGCCA[C/G]TGGATCACCTGCTCT | 29979 |
rs745467551 | snp | A/T | 1.66521e-05 | 0.00288544 | missense | UBQLN1 | GRCh38.p7 | 9:83669198 | ACCTGTGCAGCAAGG[A/T]CAGGATTCTGGCTTA | 29979 |
rs745496512 | in-del | -/AAAAAAC | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83673562 | AAAAAAAAAAAAAAA[-/AAAAAAC]AAAAAAAAAAAACTG | 29979 |
rs745524467 | in-del | -/A | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83688861 | GCGAAACTCCGTTTC[-/A]AAAAAAAAAAAAAGA | 29979 |
rs745557408 | snp | A/G | | | intron-variant, downstream-variant-500B | UBQLN1 | GRCh38.p7 | 9:83667130 | CTCACTACTACCAGA[A/G]ATGAGAAAAGTGGCA | 29979 |
rs745577379 | snp | A/T | | | intron-variant, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83706943 | AAAACAGTTTCTACG[A/T]CATAATTTTTTTTTA | 29979 |
rs745598858 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83691045 | CGGGAGGCTAAGGCA[C/T]GAGAATCACTTGAAC | 29979 |
rs745733937 | snp | A/G | 1.65548e-05 | 0.002877 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83678621 | AAAATATTTCCAAAA[A/G]AAGAAAAAAAAAAGG | 29979 |
rs745766721 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83680950 | AGAAATGAAGCTGAA[C/T]CTTGGACACAGAGCT | 29979 |
rs745835436 | snp | G/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83684617 | AGGAGTTCGTGACCA[G/T]CCTGGCCAACATGAG | 29979 |
rs745872007 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83691719 | CACGTGAGAAATCAC[A/G]TTCACTCACAAAATT | 29979 |
rs745925260 | snp | C/T | 6.59315e-05 | 0.0057412 | synonymous-codon | UBQLN1 | GRCh38.p7 | 9:83677902 | TTCTGTACGGGAAGG[C/T]TGACTACCTTCACCA | 29979 |
rs745979790 | snp | C/T | 1.69896e-05 | 0.00291454 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83661987 | AAAGGAAGCCAGTCC[C/T]TGCCACACATGACTT | 29979 |
rs746021496 | snp | C/T | 6.12464e-05 | 0.00553348 | utr-variant-5-prime, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83707691 | CCATGGCTGTGGCGG[C/T]GGCGGCGGCGGTGAC | 29979 |
rs746037438 | snp | A/C | 1.64817e-05 | 0.00287064 | synonymous-codon | UBQLN1 | GRCh38.p7 | 9:83677809 | AGTAGTGCCACCCAC[A/C]GTGCTGGCAGTGCCG | 29979 |
rs746058511 | snp | G/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83674542 | AAGGAAGCCAAGTAC[G/T]AGTGATGACTAATTT | 29979 |
rs746144812 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83697278 | AAGACATAGGCCAGG[C/T]GCGGTGGCTCACGCC | 29979 |
rs746214490 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83682239 | GCGGTGAGCCTAGAT[C/T]GCGCCACTGCACTCC | 29979 |
rs746222187 | snp | C/G | 4.94515e-05 | 0.00497225 | missense | UBQLN1 | GRCh38.p7 | 9:83683044 | CAGCTGTATTTGTTT[C/G]CTGAGCTGAATGATC | 29979 |
rs746263318 | snp | A/G | 1.64963e-05 | 0.00287192 | missense, intron-variant | UBQLN1 | GRCh38.p7 | 9:83666432 | GGATTATTCAGCATC[A/G]TCTATGGGGCAAGTG | 29979 |
rs746352370 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83699415 | GGTGCAATCATAGCT[C/T]AGTGTAACCTCCAAA | 29979 |
rs746437687 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83699298 | GACTTCAGTCCTTCC[C/T]TTTGATTAAAGTGGC | 29979 |
rs746517237 | snp | G/T | | | utr-variant-3-prime | UBQLN1 | GRCh38.p7 | 9:83660017 | TAATAAATTGTCAAA[G/T]TAGTTATGACACTAT | 29979 |
rs746523473 | snp | A/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83687412 | TGGGCCCAGGAATCT[A/T]CATTAAAAGACTGGC | 29979 |
rs746552433 | snp | C/T | 1.6473e-05 | 0.00286988 | synonymous-codon | UBQLN1 | GRCh38.p7 | 9:83679862 | TGGATTGGCCATAAT[C/T]AACTGTCTCATCAGG | 29979 |
rs746629452 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83688906 | TACATCCTTTCAAAT[A/G]CCTACCAAAAAATAG | 29979 |
rs746682367 | in-del | -/AG | 1.81717e-05 | 0.00301422 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83664980 | AAATCTGAAATTCTC[-/AG]AGAAAGTAACCATTA | 29979 |
rs746753603 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83705695 | CATAGTAACTAACTG[C/T]AAACAGCCCAGGTGA | 29979 |
rs746889796 | snp | C/T | 3.29848e-05 | 0.00406095 | synonymous-codon | UBQLN1 | GRCh38.p7 | 9:83665053 | GAGGCCCGGGGCTTC[C/T]GTTGCTAATGTCTGT | 29979 |
rs747076117 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83673660 | AACGTGAAAACTATA[C/T]GAAATTCAAATTTCA | 29979 |
rs747110717 | snp | A/G | 1.65181e-05 | 0.00287381 | missense | UBQLN1 | GRCh38.p7 | 9:83683065 | CTGAATGATCCTGAG[A/G]CCTAGGGAAAATAAT | 29979 |
rs747172644 | snp | C/T | 8.43035e-05 | 0.00649189 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83678398 | ATATTTGTGTTAAAA[C/T]AGAAGCTACTCCTTG | 29979 |
rs747178808 | snp | A/G | 1.68431e-05 | 0.00290194 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83663834 | ATTTCTAAATTTCCA[A/G]CATTAAGGAATACAA | 29979 |
rs747182082 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83664731 | CATGGCAAAGCTCCA[C/T]CTCTAAAAACAGTAA | 29979 |
rs747317393 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83679734 | TAAATAACAAATATA[C/T]CATTTTTTAGCTAAA | 29979 |
rs747367827 | snp | A/C | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83669463 | GTATCAACTGAACTA[A/C]GAAAGAACTTTAAAA | 29979 |
rs747369852 | snp | A/T | 5.42834e-05 | 0.00520949 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83669342 | GCTGAAAGTTTGTTT[A/T]TAAAAAAGACATATT | 29979 |
rs747407330 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83681372 | GAGAATAAGGCAACA[A/G]GAAAGACATCCTCAG | 29979 |
rs747412375 | in-del | -/TT | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83695202 | TGGGCCCTCCCACCT[-/TT]TTTTTTTTTTTTTTG | 29979 |
rs747497142 | snp | A/G | | | upstream-variant-2KB, intron-variant | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83709291 | GTCCAGGTGTGAGAT[A/G]ATCACTGCTTCTAAA | 29979 |
rs747615366 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83673813 | ATACTGTTATTTGTT[C/T]TGTTTTGAGACAGGG | 29979 |
rs747635590 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83698543 | AAAAGGTGGAAGCAA[C/T]CCAAGCGACCAGCAA | 29979 |
rs747677445 | snp | C/T | 1.68069e-05 | 0.00289882 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83682917 | GAAAGGAGTATTTTT[C/T]CCCATCCCTACTGGA | 29979 |
rs747729906 | snp | A/G | 1.65206e-05 | 0.00287403 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83666318 | TTCAAGCAAATCATT[A/G]CCCAAGATAGCTAAC | 29979 |
rs747845161 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83705867 | AGAAAAATACACACA[A/G]TACTATAGGCTCTAT | 29979 |
rs747869836 | snp | C/T | 2.11629e-05 | 0.00325285 | utr-variant-5-prime, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83707706 | CGGCGGCGGCGGTGA[C/T]TCAGGCAAGCAGGAG | 29979 |
rs747881776 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83685395 | AAAATTCCATACCCA[C/T]GTAAGTCTAAAGGAG | 29979 |
rs747975865 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83664875 | AGTGAGCCACAACTG[C/T]GCCCCCACACTCATA | 29979 |
rs747984811 | snp | A/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83665809 | TCGTTTTAAATAATA[A/T]AATACCATGGCAATC | 29979 |
rs748101454 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83664226 | TTGAGATCAGCTTAG[A/G]CAACATTGTTGAGAC | 29979 |
rs748181837 | snp | C/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83683271 | CAAAAAATTAGCCGG[C/G]CGTGATGGCGAGTGC | 29979 |
rs748204504 | snp | A/G | 0.000379635 | 0.0137722 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83678604 | AGTTCCAACGTCTAC[A/G]AAAAATATTTCCAAA | 29979 |
rs748271819 | snp | G/T | 0.00021767 | 0.0104301 | intron-variant, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83707455 | GGCGGCGGGCGGAGG[G/T]CCTGCCGCCACCCCC | 29979 |
rs748292711 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83672452 | TTGAATACTTAGAGG[C/T]CACTGTAGAGTTATT | 29979 |
rs748350416 | snp | C/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83700873 | ATATTCTAAGACCAA[C/G]AGGGAGCCATTAGCT | 29979 |
rs748369227 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83673450 | CTCAGGAGGCTGAGG[C/T]ACGAGAATCTCTAGA | 29979 |
rs748389627 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83680790 | GAACCTGAGGAGGAG[A/G]TCAGGGGAACCCCCA | 29979 |
rs748399925 | in-del | -/TT | | | intron-variant, utr-variant-3-prime | UBQLN1 | GRCh38.p7 | 9:83668495 | AGGCAACTTGAGGGA[-/TT]GAAAGGGTTATCGGA | 29979 |
rs748454172 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83662279 | ATATACATATACACA[C/T]ACACACACACACACA | 29979 |
rs748492001 | snp | A/T | | | synonymous-codon | UBQLN1 | GRCh38.p7 | 9:83678513 | AGCATTATATCCCCC[A/T]GGGATGCTTTCTAGG | 29979 |
rs748492724 | in-del | -/AATT | 1.66827e-05 | 0.00288809 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83661957 | ATTAAAGAAAAAAAA[-/AATT]AATCCAACTCTAAAG | 29979 |
rs748517100 | snp | A/G | 1.65021e-05 | 0.00287241 | synonymous-codon | UBQLN1 | GRCh38.p7 | 9:83677770 | AGTAGTACTCTGCCC[A/G]GAAGTGCCACTGGCA | 29979 |
rs748575749 | snp | A/C | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83696242 | TTGATATATGTAAAC[A/C]ATGTGGAGTGACTAA | 29979 |
rs748576602 | snp | A/C | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83691423 | AATAGAACAGCAATG[A/C]ATATAGCTCACTTGA | 29979 |
rs748604180 | in-del | -/A | 6.62191e-05 | 0.00575371 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83678616 | ACGAAAAATATTTCC[-/A]AAAAAAAGAAAAAAA | 29979 |
rs748637694 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83671309 | ACGTTCTTAATGACA[C/T]TGAGAATGGTGAATG | 29979 |
rs748642099 | in-del | -/A | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83687556 | GAAATATATAGGGGC[-/A]ATTCTTCTGGTTGTC | 29979 |
rs748710947 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83668702 | TCAGCAGGGGAATCA[A/G]TAGTTGAAAGAAGGA | 29979 |
rs748790024 | snp | C/T | 1.64894e-05 | 0.00287131 | missense, intron-variant | UBQLN1 | GRCh38.p7 | 9:83666420 | CCAGCAAATAGGGGA[C/T]TATTCAGCATCATCT | 29979 |
rs748839705 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83691404 | AGCTGTAATCTCAAA[A/G]TCTAATAGAACAGCA | 29979 |
rs748854944 | snp | A/G | 0.000362384 | 0.0134559 | utr-variant-5-prime, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83707728 | AAGCAGGAGGGAGCA[A/G]GCGAGCAAGGAGGAG | 29979 |
rs748881679 | snp | C/T | 1.64784e-05 | 0.00287035 | missense | UBQLN1 | GRCh38.p7 | 9:83683022 | GATGATGTAGTAACA[C/T]TGCTTCCAGCTGTAT | 29979 |
rs748914333 | snp | C/G | | | upstream-variant-2KB, nc-transcript-variant | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83708287 | GGCCCTGCGGCCGCG[C/G]CTGCGCCTGCGCGCT | 29979 |
rs748978569 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83705495 | CAATCCACCCGCCTC[A/G]GCCTCACAAAGTGCT | 29979 |
rs749021335 | snp | C/T | 1.67967e-05 | 0.00289794 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83678410 | AAACAGAAGCTACTC[C/T]TTGGCCTGAACCTTG | 29979 |
rs749028815 | snp | C/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83698224 | GCCAGTGATATTTGA[C/G]GGTAGGGGAAGAGAC | 29979 |
rs749038616 | snp | A/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83670977 | TTTTTTCTTTTTAAA[A/T]TGAGATGGAGTCTCG | 29979 |
rs749057190 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83684746 | AACCCAGAGGCAGAC[A/G]TTGCAGTGAGCTGAG | 29979 |
rs749064212 | snp | C/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83686363 | CACCACTGCACTCCA[C/G]CCTGGGTGACAGAGT | 29979 |
rs749120170 | snp | C/T | 0.00026357 | 0.0114767 | synonymous-codon | UBQLN1 | GRCh38.p7 | 9:83663974 | TGTGTTTTCACTAGG[C/T]GTGGCGTTAGATCCA | 29979 |
rs749229820 | snp | G/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83674458 | CTCATCATAGCCACT[G/T]TTTCACAAAAAATAA | 29979 |
rs749238211 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83703599 | GATACTCAAAACCTG[C/T]ATTACAAAAATCTCT | 29979 |
rs749250206 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83683154 | ACAGTGGCTCACGCC[C/T]GTAATCCCAGCACTT | 29979 |
rs749266662 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83681658 | GCATTCTTGAAACCA[C/T]AAAAACTTCAGTATG | 29979 |
rs749315539 | snp | A/G | 2.81464e-05 | 0.00375132 | synonymous-codon, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83707590 | TTTGGGCTCCGCGGA[A/G]GCAGCGGCCGCGGGG | 29979 |
rs749326643 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83693956 | GAAATTTCCTGGGCA[C/T]AATTCATTCACTAAG | 29979 |
rs749367529 | snp | C/T | 1.64874e-05 | 0.00287113 | missense | UBQLN1 | GRCh38.p7 | 9:83677796 | TGGCAGTACTACCAG[C/T]AGTGCCACCCACAGT | 29979 |
rs749373566 | snp | A/G | 2.30126e-05 | 0.00339201 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83677686 | TTTAATTATGTAAAT[A/G]AGGACAACAAAGAAA | 29979 |
rs749414179 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83682412 | TAAGCCAGGAGTTTG[A/G]GGCTGCAGTGAGCTA | 29979 |
rs749445312 | in-del | -/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83692368 | TAGAAATTTTATCAC[-/T]TAACATTTGAACGTA | 29979 |
rs749448893 | in-del | -/TT | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83697246 | CTCAGTATCTTCTGG[-/TT]TTTTTTTTTTTTTTT | 29979 |
rs749461257 | snp | C/G/T | 6.60573e-05 | 0.00574675 | intron-variant, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83707470 | TCCTGCCGCCACCCC[C/G/T]ATCCCGGCCCGAGCC | 29979 |
rs749520795 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83683087 | GAAAATAATTAATCA[C/T]AGAGTAAGCAGTAGA | 29979 |
rs749529276 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83701168 | TGATATTTATAATAT[C/T]ACAAATTAAAACTGA | 29979 |
rs749551894 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83700744 | AAAAAAGTATTAACA[A/G]GTCAGGGAACTAGAA | 29979 |
rs749571338 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83676321 | CATTAAGTATCTGAG[C/T]AAAAGGATGCAAAAC | 29979 |
rs749646980 | snp | C/T | | | utr-variant-3-prime | UBQLN1 | GRCh38.p7 | 9:83660273 | AAGTAATGCAATCAA[C/T]TTGTATTTCCCTTGA | 29979 |
rs749662906 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83662004 | GCCACACATGACTTT[C/T]AAAATTTTTTAATTG | 29979 |
rs749688956 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83701947 | AAATAAAATGTGGAA[C/T]GCTGTTGGCAACACA | 29979 |
rs749820225 | in-del | -/AAAC | 6.37599e-05 | 0.00564587 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83669372 | TAAGGAAAAATACTT[-/AAAC]AAAAGTTAAAGCTTT | 29979 |
rs749838471 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83689949 | AAAACCAGTAACAAA[C/T]GCACTGAATGGTTCA | 29979 |
rs749849813 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83677297 | ACCAGGTGCAGCGGC[C/T]CACACCTATAATCCC | 29979 |
rs749869566 | snp | C/G | | | utr-variant-3-prime | UBQLN1 | GRCh38.p7 | 9:83661573 | AATAAATGCAGAAGT[C/G]ATGCATGCAGTAGCC | 29979 |
rs749892263 | snp | C/T | 1.96088e-05 | 0.00313114 | missense, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83707520 | GGACGGAGCTATTCT[C/T]GGGCACGGCGAATTC | 29979 |
rs749932659 | snp | A/T | 1.74525e-05 | 0.00295397 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83669331 | TGAACATACTAGCTG[A/T]AAGTTTGTTTTTAAA | 29979 |
rs749987832 | snp | C/T | 8.27945e-05 | 0.00643354 | synonymous-codon | UBQLN1 | GRCh38.p7 | 9:83677752 | AGGCACCAAATTTGG[C/T]GCAGTAGTACTCTGC | 29979 |
rs749988694 | snp | A/C | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83689717 | TTGTTTTAAAGGGGC[A/C]CCATATACTGGACTA | 29979 |
rs750007311 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83663142 | GGGGAAGAGGAAAGG[A/G]AAAAGGGAAAGGGGA | 29979 |
rs750147671 | snp | C/T | | | upstream-variant-2KB, nc-transcript-variant | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83708256 | GGTTAGCGAAATTAC[C/T]AGAAAGGGACCAGTG | 29979 |
rs750177679 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83678964 | CTGACCTCGTGATCC[A/G]CCCACCTCAGCTTCC | 29979 |
rs750242442 | snp | A/C | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83680854 | CTAGAACTTGTGACC[A/C]GTATCTGAAGTAGGG | 29979 |
rs750268209 | in-del | -/AAA | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83697551 | GCAAGACACTGTCTC[-/AAA]AAAAAAAAAAAAAAA | 29979 |
rs750285139 | snp | G/T | 1.81168e-05 | 0.00300966 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83680083 | TCAAAGTCAGAAAAT[G/T]TATCATTAACATGAC | 29979 |
rs750334525 | snp | A/C | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83669785 | GATGTAATGCCTCCA[A/C]CCATTTTCACTGTGT | 29979 |
rs750481759 | snp | C/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83676528 | ATTAAGTAGAATATA[C/G]AACAGAATATTTTTA | 29979 |
rs750494165 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83705494 | GCAATCCACCCGCCT[C/T]GGCCTCACAAAGTGC | 29979 |
rs750547398 | in-del | -/TC | | | upstream-variant-2KB, intron-variant | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83709621 | GTGTGTGTGTGTGTG[-/TC]TGTCTCCCTGCATTT | 29979 |
rs750560419 | snp | C/G | 1.92025e-05 | 0.00309853 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83677997 | AATCACAAAGAATAA[C/G]CTTTTGTTTTAAATA | 29979 |
rs750679430 | snp | A/C | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83665774 | CCAGTTTCAAAACAC[A/C]AAGACTGACTTCTCT | 29979 |
rs750716408 | snp | A/C | | | intron-variant, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83706385 | TTTACAAGCACTGGG[A/C]GACAAAAACAAAAGT | 29979 |
rs750844338 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83683793 | TTTGCGAGGCCGAGG[C/T]AGGCGATCAACTGAG | 29979 |
rs750856117 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83664993 | TCAGAGAAAGTAACC[A/G]TTATACACTTTCATT | 29979 |
rs750878075 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83672186 | GTGGCTGGTGTGATC[A/G]TCTATCCAGATCACT | 29979 |
rs750901797 | snp | A/G | 1.64991e-05 | 0.00287215 | missense | UBQLN1 | GRCh38.p7 | 9:83664023 | CCAGTGCTTCCTAAT[A/G]CCCCCAAGCCAGGAG | 29979 |
rs750994406 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83703373 | TTCAATGTATACAGT[C/T]TGTTTCACTCGCAAA | 29979 |
rs751038957 | snp | C/T | | | missense | UBQLN1 | GRCh38.p7 | 9:83677778 | TCTGCCCAGAAGTGC[C/T]ACTGGCAGTACTACC | 29979 |
rs751068856 | snp | G/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83682929 | TTTTCCCATCCCTAC[G/T]GGAATGACTAAAGAC | 29979 |
rs751084193 | snp | A/T | 1.64819e-05 | 0.00287066 | synonymous-codon | UBQLN1 | GRCh38.p7 | 9:83661820 | CAGTAACCTTTCAAT[A/T]GCTGCATTGATATCA | 29979 |
rs751096134 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83671926 | AAACTGGTTGTTTCA[C/T]GTGGCCACGTTCCTT | 29979 |
rs751135614 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83700403 | TTACTGAATATGTAT[C/T]ATTGTACATAATGGA | 29979 |
rs751171413 | snp | A/G | 1.65397e-05 | 0.00287569 | missense | UBQLN1 | GRCh38.p7 | 9:83677756 | ACCAAATTTGGCGCA[A/G]TAGTACTCTGCCCAG | 29979 |
rs751185857 | snp | C/T | | | utr-variant-3-prime | UBQLN1 | GRCh38.p7 | 9:83661362 | TTACAGCATTGTTTG[C/T]AAAAATGCATGCCAA | 29979 |
rs751258653 | in-del | -/A | | | downstream-variant-500B | UBQLN1 | GRCh38.p7 | 9:83659858 | AAAAATAAAGAATGT[-/A]AAAATGTGACAAAAT | 29979 |
rs751267435 | snp | C/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83688875 | TCAAAAAAAAAAAAA[C/G]ACATGCATCTATTCT | 29979 |
rs751288571 | snp | G/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83662831 | GTAATCCCAGCACTT[G/T]GGGAGGCCAAGGCGG | 29979 |
rs751302087 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83690876 | GGCGCAGTGGCTCAC[A/G]CTTGTAATCCCAACA | 29979 |
rs751361567 | snp | C/T | 1.6486e-05 | 0.00287102 | missense | UBQLN1 | GRCh38.p7 | 9:83682980 | TTGCTAGTAGCAGAA[C/T]CAGATGTAGAGTTAC | 29979 |
rs751377892 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83690878 | CGCAGTGGCTCACGC[C/T]TGTAATCCCAACACT | 29979 |
rs751385196 | in-del | -/GT | | | upstream-variant-2KB, intron-variant | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83709588 | TCTCCAACAAATACC[-/GT]GTGTGTGTGTGTGTG | 29979 |
rs751399032 | snp | C/T | 1.648e-05 | 0.0028705 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83680089 | TCAGAAAATTTATCA[C/T]TAACATGACATAAAA | 29979 |
rs751469838 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83678912 | TTTTTTAGTAGAGAC[A/G]GGGTTTCACCGTGTT | 29979 |
rs751517088 | snp | A/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83693489 | TTTAACCAGACTGTC[A/T]AGTTCTTGTCTTGAA | 29979 |
rs751650183 | snp | G/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83686281 | ACCATAATCCCAATG[G/T]TCCAGGAGGCTGAGG | 29979 |
rs751676483 | in-del | -/GTAT | | | intron-variant, utr-variant-3-prime | UBQLN1 | GRCh38.p7 | 9:83667934 | TAGAGTAAAAAAATA[-/GTAT]GTGAGTGCTCAAGTC | 29979 |
rs751682745 | snp | C/G | 1.65679e-05 | 0.00287814 | synonymous-codon | UBQLN1 | GRCh38.p7 | 9:83664043 | CAAGCCAGGAGTAAA[C/G]CTACAGAAAGCACAA | 29979 |
rs751686466 | snp | A/G | 6.8135e-05 | 0.00583634 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83679728 | GAAAATTAAATAACA[A/G]ATATATCATTTTTTA | 29979 |
rs751780146 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83675402 | ATCATACTAAAGTCA[C/T]TTTGACAACTAAAAT | 29979 |
rs751786008 | in-del | -/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83697245 | CTCAGTATCTTCTGG[-/T]TTTTTTTTTTTTTTT | 29979 |
rs751794027 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83704356 | CTTCCACATTTTCCT[A/G]TATCTGTTTCCCTTG | 29979 |
rs751939320 | snp | G/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83665596 | AGTTCCAAATTTGAC[G/T]TTAATACATGTATCC | 29979 |
rs751950149 | snp | G/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83693637 | GCCCTGAAATGAAAA[G/T]GTATCAAGATTTAGT | 29979 |
rs751963613 | snp | G/T | 1.72636e-05 | 0.00293794 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83686183 | AAAATAAGTATGTAT[G/T]ACAGTTGTTTGCACA | 29979 |
rs752014592 | snp | A/C/T | 5.89053e-05 | 0.00542676 | synonymous-codon, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83707548 | TTCCTCCTTTTCCTT[A/C/T]GGGGTCTTCACGGTG | 29979 |
rs752020531 | snp | A/G | 1.66774e-05 | 0.00288763 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83665020 | CATTATCTTCCCCAA[A/G]TAAGCCTACCCTGGG | 29979 |
rs752040986 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83700439 | TTCATCTGTAAATAA[C/T]TTATTGAGCCCTAGG | 29979 |
rs752106164 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83694787 | ATAAACTCTGAGTCA[A/G]GTACTTTATGCATAC | 29979 |
rs752114209 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83682146 | AAAAATTAGCCGGGC[A/G]TAGTGGCACACTCCT | 29979 |
rs752136014 | snp | C/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83681270 | CAAAGTGTTTACTTC[C/G]TAAAATTACATAACC | 29979 |
rs752186853 | snp | A/C/T | 3.29583e-05 | 0.00405934 | missense | UBQLN1 | GRCh38.p7 | 9:83683011 | TATTAGGAGTTGATG[A/C/T]TGTAGTAACATTGCT | 29979 |
rs752207649 | snp | A/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83698220 | AAGAGCCAGTGATAT[A/T]TGAGGGTAGGGGAAG | 29979 |
rs752240365 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83693540 | TAAATTTTCTATTTT[C/T]AATCTGAGGAAGAAG | 29979 |
rs752275150 | snp | A/G | | | upstream-variant-2KB, intron-variant | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83710192 | TTAAGAACATATTTT[A/G]TCACAGTATCCTAAT | 29979 |
rs752293167 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83699947 | GAGCCAGTTTAATAA[C/T]GGTATCTTGAAATCT | 29979 |
rs752353119 | snp | G/T | 1.65583e-05 | 0.00287731 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83661944 | GGATTCTGTAGCTAT[G/T]AAAGAAAAAAAAAAT | 29979 |
rs752357873 | snp | A/G | 1.74257e-05 | 0.0029517 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83677974 | AAACTGTAATAAAAG[A/G]CATAAAAAATCACAA | 29979 |
rs752382531 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83677465 | TACTCGGGAGGCTGA[A/G]GCAGAAGAATCACTT | 29979 |
rs752511551 | snp | A/C | | | downstream-variant-500B | UBQLN1 | GRCh38.p7 | 9:83659806 | GCTATCTTTTTATCA[A/C]ACCACAAAAGACTGT | 29979 |
rs752524341 | snp | C/T | 1.64866e-05 | 0.00287106 | missense, intron-variant | UBQLN1 | GRCh38.p7 | 9:83666409 | GCTGAGGATTTCCAG[C/T]AAATAGGGGATTATT | 29979 |
rs752591212 | in-del | -/ACT | | | utr-variant-3-prime | UBQLN1 | GRCh38.p7 | 9:83660920 | TTTAATGCCTGTTAA[-/ACT]ACCTATGGGAGAAGC | 29979 |
rs752612881 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83690540 | TATACTGTACTTTAA[C/T]AAAAATAGTTTTAAA | 29979 |
rs752633075 | snp | C/T | 1.68417e-05 | 0.00290182 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83683105 | AGTAAGCAGTAGAGC[C/T]GATTATTTTTAAAAG | 29979 |
rs752661291 | snp | A/G | | | upstream-variant-2KB, intron-variant | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83708716 | TCTGCTGCTACGATG[A/G]CAGCTGTGCGCGAGC | 29979 |
rs752680767 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83689458 | AATTAACATATGACC[C/T]AATTGAGCATACACA | 29979 |
rs752743995 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83669060 | AAAATTGGAGACACA[A/G]TTTACTTATTTTTCT | 29979 |
rs752766787 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83696195 | CGCCTGCCATCATGA[C/T]TGTATACACTTATAA | 29979 |
rs752818789 | snp | A/G | 1.68457e-05 | 0.00290216 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83680044 | CAAGGCCACCTAAGA[A/G]GATAAAGGGCAAAAA | 29979 |
rs752865500 | snp | C/G/T | 4.96375e-05 | 0.00498164 | missense | UBQLN1 | GRCh38.p7 | 9:83665031 | CCAAATAAGCCTACC[C/G/T]TGGGATGAGGCCCGG | 29979 |
rs752872356 | snp | A/G | 1.64838e-05 | 0.00287083 | missense | UBQLN1 | GRCh38.p7 | 9:83665114 | ATTGCTCTAGGGTTT[A/G]ACATTGCTGATAGTG | 29979 |
rs752884357 | in-del | -/GGC/GGCGGC | 0.00245345 | 0.034945 | utr-variant-5-prime, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83707685 | CTCGGCCATGGCTGT[-/GGC/GGCGGC]GGCGGCGGCGGCGGC | 29979 |
rs752948283 | in-del | -/A | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83692110 | GTTTAGCTGTCTGCC[-/A]ACTCTATTTGAAACA | 29979 |
rs752948653 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83706775 | TATCAACATCGCTAT[C/T]GCCCCTCTAAAATCA | 29979 |
rs753038919 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83704880 | AGAGTAAAATAAAAG[C/T]GTTCACAGAATTTAT | 29979 |
rs753081401 | snp | C/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83704042 | AAATTTTAACTTATA[C/G]AAAACGGAATTTGTC | 29979 |
rs753104739 | snp | C/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83665480 | TCCAAAGGCACAATT[C/G]TTACGACGTGGATAT | 29979 |
rs753108015 | snp | A/C | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83674226 | ACCAATCATGCCAGA[A/C]CAAGAAAAAAGGAAG | 29979 |
rs753130602 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83675175 | TAACCACACAGAAGG[C/T]TGATGGTGGCTTAGC | 29979 |
rs753184562 | snp | G/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83692454 | TAAATAGTATTGATA[G/T]GGAAAAACTTAATTA | 29979 |
rs753194857 | in-del | -/AAAC | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83682491 | CTCTCTTAAAAAAAC[-/AAAC]AAACAAACAAACAAA | 29979 |
rs753200142 | snp | C/T | 4.62054e-05 | 0.0048063 | missense, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83707576 | GTGACTTTCATGATT[C/T]TGGGCTCCGCGGAGG | 29979 |
rs753240706 | snp | C/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83705047 | GGAGGCATGAATTAG[C/G]AATCCTAGAAAAGAG | 29979 |
rs753318577 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83664373 | GAAGTGAGCTGAGAT[C/T]GCGCCACTGCACTCC | 29979 |
rs753377065 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83703837 | AAAAAATTAAGGCAA[C/T]CTGTTTCTGCCTGTT | 29979 |
rs753388544 | snp | A/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83663288 | TAATAAAACAGGTTT[A/T]AACTGGCGATCATCT | 29979 |
rs753391454 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83692240 | GTGTTTTTATCTAAA[C/T]GGAATTTGTCCTACA | 29979 |
rs753402137 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83679078 | GCAGACCACAACAAA[C/T]CAAAATAGAGCCACT | 29979 |
rs753438226 | in-del | -/AAAAG | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83694733 | AATTCACCGGTGAAC[-/AAAAG]GCTGTGGGGAAAGAA | 29979 |
rs753504412 | snp | C/T | 3.29788e-05 | 0.00406058 | missense | UBQLN1 | GRCh38.p7 | 9:83664014 | GAAGAGCCTCCAGTG[C/T]TTCCTAATGCCCCCA | 29979 |
rs753520820 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83698004 | GCCTCCCAGAGTGCC[A/G]GGATTAGCAGCATGA | 29979 |
rs753596592 | snp | C/T | | | upstream-variant-2KB, intron-variant | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83708991 | GAATGTACAAACCAG[C/T]CCATTATTAATCAAT | 29979 |
rs753738865 | snp | C/G | | | downstream-variant-500B | UBQLN1 | GRCh38.p7 | 9:83659690 | CACCTATAAGCCTCA[C/G]CACCACATGTATAAT | 29979 |
rs753742195 | snp | A/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83670798 | CAAAGTTTATGAAAC[A/T]TTCTGAATTCGTTGT | 29979 |
rs753870790 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83707255 | TCGGCGGATACCAGA[A/G]AAGGAAGGCTCCGAG | 29979 |
rs753912493 | snp | A/C | | | intron-variant, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83706500 | TTAAACCAATACCCC[A/C]ATCACCTACTGTCCC | 29979 |
rs753921533 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83666909 | AAAGGACCACTACAT[C/T]TACCTGCCTACTACA | 29979 |
rs753929720 | in-del | -/A | 7.04734e-05 | 0.00593563 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83677977 | TGTAATAAAAGACAT[-/A]AAAAAATCACAAAGA | 29979 |
rs753981656 | snp | C/T | 0.000106775 | 0.00730589 | missense, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83707667 | GACCGCCGCTTTCAC[C/T]ACTCTCGGCCATGGC | 29979 |
rs754033830 | in-del | -/AGCACCTTCGGCTCCGGCGGCGCT | 3.94438e-05 | 0.00444076 | cds-indel, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83707610 | GGCCGCGGGGGCGCC[-/AGCACCTTCGGCTCCGGCGGCGCT]AGCACCTTCGGCTCC | 29979 |
rs754067113 | snp | A/G | 1.65042e-05 | 0.0028726 | synonymous-codon | UBQLN1 | GRCh38.p7 | 9:83682964 | ACCTAAACCAAAAGG[A/G]TTGCTAGTAGCAGAA | 29979 |
rs754101768 | in-del | -/ATAT | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83662265 | TGTGTGTATATACAT[-/ATAT]ATACATATACACACA | 29979 |
rs754150159 | snp | A/G | 1.80527e-05 | 0.00300433 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83677988 | GACATAAAAAATCAC[A/G]AAGAATAAGCTTTTG | 29979 |
rs754163063 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83696032 | GCAACCTCCACCTCC[C/T]GGATTCAAGCGATTC | 29979 |
rs754184661 | snp | C/T | | | missense | UBQLN1 | GRCh38.p7 | 9:83679884 | CTCATCAGGTCAGGA[C/T]TTGAGAGCATGCTCT | 29979 |
rs754241673 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83673261 | AAACAATTTTTGGTC[A/G]GGTGCAGTGACTTAC | 29979 |
rs754307727 | snp | A/C | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83682243 | TGAGCCTAGATCGCG[A/C]CACTGCACTCCAGCC | 29979 |
rs754313264 | snp | A/G | 4.94401e-05 | 0.00497168 | missense | UBQLN1 | GRCh38.p7 | 9:83677895 | CTCTATTTTCTGTAC[A/G]GGAAGGTTGACTACC | 29979 |
rs754346292 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83703114 | CTTGCTCGTGGATAC[C/T]TGGAAATCCTCAAAG | 29979 |
rs754405565 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83692340 | TTTTCAGATTACACT[A/G]TCTTCAAAATTTCTA | 29979 |
rs754458125 | in-del | -/AAACAAAC | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83682487 | CTGCCTCTCTTAAAA[-/AAACAAAC]AAACAAACAAACAAA | 29979 |
rs754498025 | snp | A/C | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83679213 | TTCCCTCCATTTTAA[A/C]CCTATTAGGAAAGTA | 29979 |
rs754517006 | snp | A/G | 1.68829e-05 | 0.00290537 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83682903 | ACTACCCAGGAAGGG[A/G]AAGGAGTATTTTTTC | 29979 |
rs754577466 | snp | C/G | | | upstream-variant-2KB, intron-variant | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83709031 | TTTAAATCCTGACAG[C/G]CCACTATGACCCAAA | 29979 |
rs754633861 | snp | C/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83698486 | CCTTAAAATATTTTA[C/G]ACATACTGGGTTAAA | 29979 |
rs754666555 | snp | A/G | | | upstream-variant-2KB, intron-variant | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83710024 | AATAATCATAGCTAT[A/G]TTTACTAAAAACTCT | 29979 |
rs754741483 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83669858 | GAAACCATAGAGCAC[A/G]GTGACTCCAAGCAGT | 29979 |
rs754755292 | snp | A/G | | | downstream-variant-500B | UBQLN1 | GRCh38.p7 | 9:83659708 | CCACATGTATAATAA[A/G]GAAACCATGACGCCT | 29979 |
rs754786533 | snp | C/T | 1.64846e-05 | 0.0028709 | synonymous-codon, intron-variant | UBQLN1 | GRCh38.p7 | 9:83666383 | GAGCTGTTGTCTCAT[C/T]TGTTCTTGAAGCTGA | 29979 |
rs754875499 | snp | A/C | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83687262 | GGCTTTCCAGGGACC[A/C]GACACATAAAACCAG | 29979 |
rs754925709 | snp | C/T | 1.64825e-05 | 0.00287071 | missense | UBQLN1 | GRCh38.p7 | 9:83682987 | TAGCAGAACCAGATG[C/T]AGAGTTACTATTAGG | 29979 |
rs754961105 | in-del | -/TTTAAT | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83704513 | CTACTTCAGAAAGAC[-/TTTAAT]TTTATCTATTAACAA | 29979 |
rs754966029 | snp | A/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83688353 | AGGATTCAAACTTAG[A/T]TTTGACTTCAAAGAC | 29979 |
rs754980950 | snp | A/G | 1.7011e-05 | 0.00291637 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83679731 | AATTAAATAACAAAT[A/G]TATCATTTTTTAGCT | 29979 |
rs755010264 | in-del | -/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83696525 | CGCCTGCAGTCCCAG[-/T]TTTCTTCAGAAGCTG | 29979 |
rs755014786 | in-del | -/GGC | 0.197531 | 0.244432 | utr-variant-5-prime, upstream-variant-2KB, cds-indel | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83707686 | CTCGGCCATGGCTGT[-/GGC]GGCGGCGGCGGCGGT | 29979 |
rs755015487 | snp | A/C | 1.66021e-05 | 0.0028811 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83664048 | CAGGAGTAAACCTAC[A/C]GAAAGCACAAATAGG | 29979 |
rs755020398 | snp | A/G | 1.69387e-05 | 0.00291016 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83665190 | AAGGAATTAAAATCA[A/G]TGAACGTAAATTTTT | 29979 |
rs755032298 | in-del | -/AAATAA | 4.7719e-05 | 0.00488439 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83678008 | ATAAGCTTTTGTTTT[-/AAATAA]GATATGAAACTTTTT | 29979 |
rs755061326 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83695050 | TAACACAAGTAGAAC[A/G]AGTAAGATAAAGAAA | 29979 |
rs755072549 | snp | A/C | 8.31552e-05 | 0.00644754 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83665023 | TATCTTCCCCAAATA[A/C]GCCTACCCTGGGATG | 29979 |
rs755112041 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83703639 | AGCACCTTGGAATGT[A/G]CACAGTGCAGTTTAT | 29979 |
rs755178042 | in-del | -/CA | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83662269 | GTGTATATACATATA[-/CA]TATACACACACACAC | 29979 |
rs755188903 | in-del | -/T | | | intron-variant, utr-variant-3-prime | UBQLN1 | GRCh38.p7 | 9:83668308 | AACCATTCATTTGAC[-/T]TTAAAGCTTTTAAAA | 29979 |
rs755228553 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83673321 | AGGCAGACAGATCAC[C/T]CAAGGTCGGGAGTTT | 29979 |
rs755284580 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83672283 | GCACTTATAATTTTC[C/T]TCAAGAACTTTTCCT | 29979 |
rs755314233 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83680180 | ACAAATCGAATACCT[A/G]TTACTAATATTTAAT | 29979 |
rs755325614 | snp | C/T | 1.92487e-05 | 0.00310226 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83669357 | TTAAAAAAGACATAT[C/T]AAGGAAAAATACTTA | 29979 |
rs755380452 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83704699 | GTGTGGTGTGGCATG[C/T]GCCTGTAGTCTCAGC | 29979 |
rs755489163 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83674155 | ACAGTGAATCAGTTA[C/T]ACTCATGCAGCACAA | 29979 |
rs755506407 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83703249 | ATACAGGTTGAGCAT[C/T]CCCAATCCAAAAATA | 29979 |
rs755530093 | snp | A/C | | | downstream-variant-500B | UBQLN1 | GRCh38.p7 | 9:83659535 | ATCCTTTAAGTGCTG[A/C]TAAGAATTTTAAGTA | 29979 |
rs755578075 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83664375 | AGTGAGCTGAGATCG[C/T]GCCACTGCACTCCAG | 29979 |
rs755633438 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83689720 | TTTTAAAGGGGCACC[A/G]TATACTGGACTATCA | 29979 |
rs755636055 | snp | A/G | 5.06941e-05 | 0.00503433 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83685953 | TAGTTACTTTTAGAA[A/G]TACGAACATTTATCC | 29979 |
rs755663112 | snp | A/T | 3.29745e-05 | 0.00406031 | missense, intron-variant | UBQLN1 | GRCh38.p7 | 9:83666411 | TGAGGATTTCCAGCA[A/T]ATAGGGGATTATTCA | 29979 |
rs755789718 | snp | A/G | | | upstream-variant-2KB, nc-transcript-variant | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83708259 | TAGCGAAATTACTAG[A/G]AAGGGACCAGTGGGC | 29979 |
rs755794879 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83678225 | ACGGGATTTCACCGT[A/G]TTAGCCAGGATGGTC | 29979 |
rs755830805 | snp | G/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83694182 | TATCCAAAAGTAAAA[G/T]TTACTTCAGCTCTGA | 29979 |
rs755858175 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83673303 | TAGCACTTTGGGAGG[C/T]CAAGGCAGACAGATC | 29979 |
rs755884411 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83669838 | GGTAGGCACATTTAA[C/T]ATTTGAAACCATAGA | 29979 |
rs755897986 | snp | G/T | 1.6516e-05 | 0.00287362 | missense | UBQLN1 | GRCh38.p7 | 9:83663879 | AGAACTGATACCTGA[G/T]GATTTACTCCAGCAA | 29979 |
rs755966937 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83705263 | TTTTTTTTTTGAAAC[A/G]GAGTTTCACTCTTGT | 29979 |
rs755982850 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83696292 | CACCTCTCTTATCTT[C/T]TTTGTAGTTGCAGCT | 29979 |
rs756078530 | snp | G/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83665746 | TTGCATAATACATGA[G/T]GCCCTAGAACTACCA | 29979 |
rs756116588 | snp | C/T | 4.94539e-05 | 0.00497238 | missense | UBQLN1 | GRCh38.p7 | 9:83665118 | CTCTAGGGTTTGACA[C/T]TGCTGATAGTGTATC | 29979 |
rs756153558 | snp | A/C | 2.67921e-05 | 0.00365996 | missense, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83707586 | TGATTTTGGGCTCCG[A/C]GGAGGCAGCGGCCGC | 29979 |
rs756236651 | snp | A/C | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83666893 | GAAAATCTAGATCTG[A/C]AAAGGACCACTACAT | 29979 |
rs756306613 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83694905 | GCTCCTTACCCATCA[C/T]CAGATTTCTCCAATT | 29979 |
rs756313891 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83705533 | CAGGTGTGAGCCACC[A/G]CATCCGGCCCAGAAG | 29979 |
rs756332478 | in-del | -/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83678974 | GATCCGCCCACCTCA[-/G]CTTCCCAAAGTGCTG | 29979 |
rs756343425 | in-del | -/AA | | | intron-variant, utr-variant-3-prime | UBQLN1 | GRCh38.p7 | 9:83667779 | CAAGTTTTTACACTC[-/AA]GAGTCTTTTTAAATA | 29979 |
rs756390665 | snp | A/G | | | synonymous-codon | UBQLN1 | GRCh38.p7 | 9:83683036 | ATTGCTTCCAGCTGT[A/G]TTTGTTTGCTGAGCT | 29979 |
rs756397826 | in-del | -/CCAGAAGTGCCACTGGCAGTACTA | 3.30256e-05 | 0.00406346 | cds-indel | UBQLN1 | GRCh38.p7 | 9:83677767 | GCAGTAGTACTCTGC[-/CCAGAAGTGCCACTGGCAGTACTA]CCAGAAGTGCCACTG | 29979 |
rs756458336 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83678237 | CGTATTAGCCAGGAT[A/G]GTCTTGATCTCCTGA | 29979 |
rs756515927 | snp | C/T | 1.64768e-05 | 0.00287021 | missense | UBQLN1 | GRCh38.p7 | 9:83677880 | GATTGGGTAGTGGAT[C/T]TCTATTTTCTGTACG | 29979 |
rs756561963 | snp | C/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83700593 | GGATCCCAATCCAGT[C/G]TGGACAATCAGAAAT | 29979 |
rs756567383 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83661948 | TCTGTAGCTATTAAA[A/G]AAAAAAAAAATTAAT | 29979 |
rs756587245 | snp | C/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83672198 | ATCGTCTATCCAGAT[C/G]ACTACAATTTTCTCC | 29979 |
rs756652236 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83701910 | AAAGTAGAAACAACC[C/T]AATGTCCACCACGTG | 29979 |
rs756702819 | snp | G/T | | | upstream-variant-2KB, intron-variant | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83709884 | GCCAAAAAAAAAAAT[G/T]TGCAAAAACCGCAAT | 29979 |
rs756702954 | snp | A/G | 9.48902e-05 | 0.00688739 | synonymous-codon, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83707656 | GGAGCCCGGAGGACC[A/G]CCGCTTTCACCACTC | 29979 |
rs756716078 | snp | A/G | 3.33211e-05 | 0.0040816 | missense | UBQLN1 | GRCh38.p7 | 9:83669196 | TCACCTGTGCAGCAA[A/G]GTCAGGATTCTGGCT | 29979 |
rs756774743 | snp | C/G | 1.65828e-05 | 0.00287943 | missense | UBQLN1 | GRCh38.p7 | 9:83669286 | GGTTTTCAGTTATTT[C/G]TTGCAACAAGCTCTG | 29979 |
rs756874367 | snp | A/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83676821 | ATTTCTTCCTACTTA[A/T]ACGCCAAGTATTAGG | 29979 |
rs756880275 | in-del | -/CTGT | | | upstream-variant-2KB, intron-variant | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83709488 | TCCCCTTGCCTTCAC[-/CTGT]CTGTCTAACTTCTAC | 29979 |
rs756950951 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83689702 | AAAAAGACCTAACCA[C/T]TGTTTTAAAGGGGCA | 29979 |
rs756952372 | snp | A/G | 6.74684e-05 | 0.00580772 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83685959 | CTTTTAGAAGTACGA[A/G]CATTTATCCACAATT | 29979 |
rs757041044 | snp | C/G | | | missense | UBQLN1 | GRCh38.p7 | 9:83677918 | TGACTACCTTCACCA[C/G]AGGATGTATTGCTCA | 29979 |
rs757080256 | snp | C/T | 5.08246e-05 | 0.00504081 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83679742 | AAATATATCATTTTT[C/T]AGCTAAACGAACTGA | 29979 |
rs757086156 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83690967 | ACATGGCAAAACCCC[A/G]TCTCTGCTAAAAATA | 29979 |
rs757127935 | snp | A/G | | | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83708110 | CCAAAGTGCAGGCGA[A/G]GCCAGTGTGAAGGAC | 29979 |
rs757144294 | snp | C/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83696204 | TCATGATTGTATACA[C/G]TTATAAAGTACAACA | 29979 |
rs757234071 | snp | A/G | 0.000108654 | 0.0073699 | synonymous-codon, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83707668 | ACCGCCGCTTTCACC[A/G]CTCTCGGCCATGGCT | 29979 |
rs757291171 | snp | A/G | 1.648e-05 | 0.0028705 | synonymous-codon | UBQLN1 | GRCh38.p7 | 9:83677896 | TCTATTTTCTGTACG[A/G]GAAGGTTGACTACCT | 29979 |
rs757421024 | snp | A/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83705402 | TTACAGGTGCCTGCC[A/T]CCACGCCCAGCTAAG | 29979 |
rs757484993 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83704359 | CCACATTTTCCTGTA[C/T]CTGTTTCCCTTGCAT | 29979 |
rs757531706 | snp | A/C | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83664738 | AAGCTCCATCTCTAA[A/C]AACAGTAACAACAAC | 29979 |
rs757565634 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83693714 | GCTTACTCCCTGTTC[C/T]CAATTGTTTTTGAGA | 29979 |
rs757602619 | in-del | -/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83697247 | TCAGTATCTTCTGGT[-/T]TTTTTTTTTTTTTTT | 29979 |
rs757617430 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83665633 | TAGCTTTACTACTTC[C/T]AAATATACACCACCT | 29979 |
rs757622952 | snp | A/G | 1.648e-05 | 0.0028705 | synonymous-codon | UBQLN1 | GRCh38.p7 | 9:83683030 | AGTAACATTGCTTCC[A/G]GCTGTATTTGTTTGC | 29979 |
rs757668663 | snp | A/G | 1.64985e-05 | 0.0028721 | synonymous-codon | UBQLN1 | GRCh38.p7 | 9:83663890 | CTGAGGATTTACTCC[A/G]GCAAGAGCCTGCAGC | 29979 |
rs757713388 | in-del | -/CAGAACTCAATC | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83681384 | CAAGAAAGACATCCT[-/CAGAACTCAATC]CAGAACTCAATCTAG | 29979 |
rs757733212 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83682178 | TAATCCCAGCTACTC[A/G]GGAGGCTGAGGCAGA | 29979 |
rs757802815 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83700680 | GGGCAAAGAGTGTTC[C/T]TGCATTCTAGGTAGC | 29979 |
rs757807830 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83682141 | TACAAAAAAATTAGC[C/T]GGGCGTAGTGGCACA | 29979 |
rs757823114 | snp | C/G | | | missense | UBQLN1 | GRCh38.p7 | 9:83682989 | GCAGAACCAGATGTA[C/G]AGTTACTATTAGGAG | 29979 |
rs757838841 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83675785 | AGTCAGTCAAGTCTC[A/G]CTACATATCAGTATT | 29979 |
rs757843255 | snp | G/T | 1.8818e-05 | 0.00306735 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83677991 | ATAAAAAATCACAAA[G/T]AATAAGCTTTTGTTT | 29979 |
rs757897569 | snp | A/T | 0.000120053 | 0.00774675 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83661971 | AAATTAATCCAACTC[A/T]AAAGGAAGCCAGTCC | 29979 |
rs757898207 | snp | A/G | 0.000148946 | 0.00862849 | missense | UBQLN1 | GRCh38.p7 | 9:83677753 | GGCACCAAATTTGGC[A/G]CAGTAGTACTCTGCC | 29979 |
rs757983710 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83699254 | CATGATAAATTTTGT[C/T]ATGTGTGAGTCACCA | 29979 |
rs757999895 | snp | A/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83687315 | TATAAAGAAACACTT[A/T]CTTATACTATTCTCA | 29979 |
rs758074019 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83700115 | CTAAAATTATATTCA[C/T]TATGAACCATCTTTG | 29979 |
rs758214415 | in-del | -/TC | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83703711 | TGTTACTCAGTTGAT[-/TC]TGAGTGCTCCGTGAA | 29979 |
rs758271314 | in-del | -/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83695632 | AGTTAAAAAAAAAAA[-/T]TACCCCCAAGTTTTA | 29979 |
rs758285730 | snp | C/T | 1.64874e-05 | 0.00287113 | synonymous-codon | UBQLN1 | GRCh38.p7 | 9:83665128 | TGACATTGCTGATAG[C/T]GTATCAGGATTCTGC | 29979 |
rs758310808 | snp | C/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83666175 | ACATAAGCAAAAGGT[C/G]AGCAGTGAAATGGGA | 29979 |
rs758388099 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83677610 | ATGAAAAATATAGTT[C/T]ATAAAAGATACTCAC | 29979 |
rs758390099 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83666937 | ACAAAACAGCTAATA[C/T]TAGGTCCAAAAAAAT | 29979 |
rs758398503 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83705628 | CAAGTCTAAGTATAT[A/G]ACCATGAAAGATAAA | 29979 |
rs758541941 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83705044 | GGTGGAGGCATGAAT[C/T]AGGAATCCTAGAAAA | 29979 |
rs758560361 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83703769 | AAAGCTTAAGCTTTA[C/T]TAGTAACCTTGAACA | 29979 |
rs758611768 | snp | A/G | 2.03739e-05 | 0.00319163 | utr-variant-5-prime, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83707692 | CATGGCTGTGGCGGC[A/G]GCGGCGGCGGTGACT | 29979 |
rs758624230 | snp | A/C | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83703468 | CTGAATTTCATGTTT[A/C]TATTTAGGTGCCATC | 29979 |
rs758663402 | snp | G/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83673483 | CTGGGAGGCAGAGGT[G/T]GCAGTGAGCCGTGAT | 29979 |
rs758665469 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83685705 | TTACTCATGATCTTT[A/G]TCTAAAAATTTCCTT | 29979 |
rs758691023 | snp | A/C | 0.000234119 | 0.0108169 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83686163 | TCCTTAAACTAAATA[A/C]AAATAAAATAAGTAT | 29979 |
rs758755328 | snp | A/C | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83674256 | GAAGGAGAGTTACAA[A/C]TGTCAGGTTTTTAAG | 29979 |
rs758811841 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83704047 | TTAACTTATAGAAAA[C/T]GGAATTTGTCTGATA | 29979 |
rs758853425 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83684568 | TGTAATCCCAGCACT[C/T]TGGGAGGCCAAGGCT | 29979 |
rs758886515 | in-del | -/AAA | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83705196 | CATTGGCGGGATGGT[-/AAA]AAAATGATACAAGCA | 29979 |
rs758903835 | snp | C/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83692470 | GGAAAAACTTAATTA[C/G]CCATCTTAGAAAATC | 29979 |
rs758959786 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83681339 | TATATATGCCAGAGA[C/T]TGTGTTACATATGTA | 29979 |
rs758967747 | in-del | -/AAAC | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83684023 | AGACTCTTGAAAAAC[-/AAAC]AAACAAACAAACAAA | 29979 |
rs758997275 | snp | A/G | 1.65809e-05 | 0.00287926 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83663860 | TACAAAACTTGAATG[A/G]AAAAGAACTGATACC | 29979 |
rs759006960 | snp | C/T | 1.6501e-05 | 0.00287232 | synonymous-codon | UBQLN1 | GRCh38.p7 | 9:83664025 | AGTGCTTCCTAATGC[C/T]CCCAAGCCAGGAGTA | 29979 |
rs759008179 | snp | G/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83704997 | TGATTATTTCTAATC[G/T]TTTGCAGTAAAATGC | 29979 |
rs759009459 | in-del | -/TTG | 1.64944e-05 | 0.00287175 | cds-indel, intron-variant | UBQLN1 | GRCh38.p7 | 9:83666350 | TCTTGTCTTACTCAC[-/TTG]TTGGAGGAAAGTTGG | 29979 |
rs759033230 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83675969 | AATTTGTGGGAATTT[A/G]TTTTGTCTCTTGATG | 29979 |
rs759117365 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83665973 | AGAAAACCTATAAAA[C/T]AGAATAGGGTAGCTC | 29979 |
rs759187115 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83682699 | CATACTAAATTATGT[A/G]GTAGTCAGATCAGGT | 29979 |
rs759187667 | in-del | -/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83670953 | AGTCAGTGTTCATGC[-/T]CCACCTCTTTTTTTC | 29979 |
rs759205291 | snp | G/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83693506 | GTTCTTGTCTTGAAA[G/T]CATACCTTCTTTCTC | 29979 |
rs759273610 | snp | C/T | 3.6865e-05 | 0.00429315 | missense | UBQLN1 | GRCh38.p7 | 9:83686119 | ACACAAGTTGGTCAG[C/T]ATGTGATTTAAAACG | 29979 |
rs759327611 | snp | A/G | 0.000164756 | 0.00907472 | missense | UBQLN1 | GRCh38.p7 | 9:83677831 | GCAGTGCCGCTGGAA[A/G]CTGATGAACTCTGGG | 29979 |
rs759423809 | snp | G/T | 1.72454e-05 | 0.00293639 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83669134 | CAATTACAAGATTAG[G/T]TTATTTTAATTCACA | 29979 |
rs759439779 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83699892 | TCTGCCCTAAGGCAC[C/T]CATTATAAGCAATGG | 29979 |
rs759458939 | snp | A/G | 1.6476e-05 | 0.00287014 | synonymous-codon | UBQLN1 | GRCh38.p7 | 9:83663989 | TGTGGCGTTAGATCC[A/G]TTAGTTCCCGAAGAG | 29979 |
rs759527590 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83701240 | ATATTAATAAAAATA[A/G]CATCCTTATGAAAAA | 29979 |
rs759635618 | snp | A/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83669012 | TAATTACATATGAAG[A/T]ATTAATTTACTGCAA | 29979 |
rs759683659 | snp | C/T | 1.64947e-05 | 0.00287177 | synonymous-codon | UBQLN1 | GRCh38.p7 | 9:83680012 | CAAACCCAAGCTACT[C/T]AGACCTGCAAGTCCC | 29979 |
rs759818042 | snp | C/T | | | upstream-variant-2KB, intron-variant | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83709359 | AATTTCTTCCATATG[C/T]CTAAATAAAATTTCT | 29979 |
rs759818848 | snp | G/T | | | intron-variant, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83706673 | CACCAAGAATCTTAA[G/T]TAACTGCAAGATTTG | 29979 |
rs759937517 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83698656 | GGTGGCTCACACTTG[C/T]ATAATCCTAGCATTT | 29979 |
rs759939462 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83685340 | AAAAATATGGACACT[A/G]ACAACTAAGTCTTCG | 29979 |
rs760027933 | snp | A/G | 8.29194e-05 | 0.00643839 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83682941 | TACTGGAATGACTAA[A/G]GACACTTACCTAAAC | 29979 |
rs760100614 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83686618 | GACCAAATTTAGTTC[A/G]AGCCACAGTTAGCTC | 29979 |
rs760111578 | in-del | -/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83673591 | AAAACTGCGCTTACG[-/T]TTTTTATTTTTAAAT | 29979 |
rs760118331 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83673783 | AGAAACTGTCTATGG[C/T]ACTGTCACTCCTTCA | 29979 |
rs760201921 | snp | A/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83682150 | ATTAGCCGGGCGTAG[A/T]GGCACACTCCTATAA | 29979 |
rs760239913 | snp | A/G | 8.23988e-05 | 0.00641815 | missense | UBQLN1 | GRCh38.p7 | 9:83663999 | GATCCATTAGTTCCC[A/G]AAGAGCCTCCAGTGC | 29979 |
rs760296955 | snp | C/T | 3.34885e-05 | 0.00409184 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83664077 | GGAAATATCCTAAGG[C/T]CCTGCAAAACCAGAA | 29979 |
rs760303853 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83704595 | ACTTTGGGAAGCCGA[A/G]GCAGGCGGATCACAA | 29979 |
rs760320235 | in-del | -/CTTTTTTT | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83671662 | GTGCTGTCATCCAGG[-/CTTTTTTT]CTTTTTTTCTTTTTT | 29979 |
rs760381937 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83662606 | CCTGATAATTTGGAG[A/G]CTTGTAAGTTAACTT | 29979 |
rs760395060 | in-del | -/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83690214 | AATGTCCCTCAACTG[-/T]AAAATAAACTATAGT | 29979 |
rs760409823 | snp | C/T | 1.68083e-05 | 0.00289894 | synonymous-codon | UBQLN1 | GRCh38.p7 | 9:83677731 | TAAAAGCATACCTCC[C/T]ACTCCAGGCACCAAA | 29979 |
rs760430898 | snp | A/G | 1.65015e-05 | 0.00287237 | intron-variant, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83707488 | CCCGGCCCGAGCCCC[A/G]GGCGGCCTCACCTGC | 29979 |
rs760476779 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83680924 | GACACTAACTGTAGG[C/T]AGGTAGTATCAGAAA | 29979 |
rs760604685 | snp | C/T | | | upstream-variant-2KB, intron-variant | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83709808 | GAGGTGGGGGCACTA[C/T]GGTGTAAATCAGAGA | 29979 |
rs760669385 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83690072 | TAACATTTTGCAACA[A/G]AAGTTGAACATATGC | 29979 |
rs760672242 | snp | C/T | 1.95074e-05 | 0.00312303 | synonymous-codon | UBQLN1 | GRCh38.p7 | 9:83686126 | TTGGTCAGTATGTGA[C/T]TTAAAACGTTTAGAG | 29979 |
rs760691905 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83677502 | AGGAGGAAGAGGTTG[C/T]GGTGAGCTGAGATCG | 29979 |
rs760828298 | snp | A/C | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83662604 | TACCTGATAATTTGG[A/C]GGCTTGTAAGTTAAC | 29979 |
rs760831264 | snp | A/T | 1.64882e-05 | 0.00287121 | missense, intron-variant | UBQLN1 | GRCh38.p7 | 9:83666364 | CTTGTTGGAGGAAAG[A/T]TGGGAGCTGTTGTCT | 29979 |
rs760844397 | snp | C/T | | | intron-variant, utr-variant-3-prime | UBQLN1 | GRCh38.p7 | 9:83667526 | CAGGAACATACAGTA[C/T]TTATTTCAAAGTGAC | 29979 |
rs760864358 | snp | A/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83690437 | CCTTAAGTTTGCAAG[A/T]GACTTCTTGGGAGTT | 29979 |
rs760864830 | snp | A/G | 1.70583e-05 | 0.00292042 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83680053 | CTAAGAGGATAAAGG[A/G]CAAAAACATACAAAT | 29979 |
rs761010047 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83692718 | TTATCCAGGCATGGT[A/G]GCAAATGCCTGTAAT | 29979 |
rs761024728 | snp | C/T | 1.65296e-05 | 0.00287481 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83666464 | TCAAACAATTTTAAC[C/T]GGAAATATCTGAAAC | 29979 |
rs761026149 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83678739 | TTAATTTTTTTGAGA[C/T]GGAGTCTTGCTTTGT | 29979 |
rs761062931 | snp | A/G/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83696003 | AGAGTGCAGTCGCAC[A/G/T]ATCTCAGCTCACTGC | 29979 |
rs761082246 | snp | A/T | | | upstream-variant-2KB, intron-variant, nc-transcript-variant | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83708424 | GCGTTCCCCGCTGGG[A/T]GGAGGGTCTGGTGAT | 29979 |
rs761135602 | snp | C/G | 1.7557e-05 | 0.0029628 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83677975 | AACTGTAATAAAAGA[C/G]ATAAAAAATCACAAA | 29979 |
rs761220483 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83683856 | GTAAAACCCTATCTC[C/T]ACTAAAATACAAAAA | 29979 |
rs761241164 | snp | C/T | 2.11401e-05 | 0.00325109 | missense, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83707504 | GGCGGCCTCACCTGC[C/T]GGACGGAGCTATTCT | 29979 |
rs761242402 | snp | A/C | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83683777 | CCTGTAATCCCAGCA[A/C]TTTGCGAGGCCGAGG | 29979 |
rs761271099 | snp | A/G | 2.03015e-05 | 0.00318596 | missense | UBQLN1 | GRCh38.p7 | 9:83686134 | TATGTGATTTAAAAC[A/G]TTTAGAGATTTCTTC | 29979 |
rs761307790 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83704297 | ATCTTTTGTGCTTCA[A/G]GTAGATTTTACAAAT | 29979 |
rs761320356 | snp | G/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83679049 | TTTGGACCAGCCTCC[G/T]GCACTATGCCCCAGC | 29979 |
rs761332149 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83673120 | CTGTAATCCCAGCTA[C/T]TGGGGAGGCTGAGAA | 29979 |
rs761332345 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83685039 | GAATGCCTGGGTACA[C/T]TGTTGTATCATATGT | 29979 |
rs761421384 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83681647 | AATGTATTAATGCAT[C/T]CTTGAAACCACAAAA | 29979 |
rs761465650 | snp | A/T | 1.80033e-05 | 0.00300022 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83664984 | CTGAAATTCTCAGAG[A/T]AAGTAACCATTATAC | 29979 |
rs761566911 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83702817 | GATGATGACCCTAAG[A/G]CAAGTTGCCTTATCA | 29979 |
rs761576280 | in-del | -/AAC | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83663666 | CTTCTCTACAACCGT[-/AAC]AACGTTTCCTTTAGT | 29979 |
rs761577712 | snp | A/T | 1.64806e-05 | 0.00287054 | missense | UBQLN1 | GRCh38.p7 | 9:83677814 | TGCCACCCACAGTGC[A/T]GGCAGTGCCGCTGGA | 29979 |
rs761612608 | snp | C/T | | | utr-variant-3-prime | UBQLN1 | GRCh38.p7 | 9:83661475 | ACTACCATAGGCTAA[C/T]GTTTAAAAAGCAAAT | 29979 |
rs761746549 | in-del | -/AAAAT | 1.66521e-05 | 0.00288544 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83686163 | TCCTTAAACTAAATA[-/AAAAT]AAAATAAGTATGTAT | 29979 |
rs761778338 | in-del | -/A | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83672544 | ACAAGTGGAACAGCC[-/A]GTCAGTTGAACAGTC | 29979 |
rs761784302 | snp | A/C | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83691828 | TAGTCTTGAAGTATG[A/C]ATTTATGGCACTTCA | 29979 |
rs761784818 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83671317 | AATGACATTGAGAAT[A/G]GTGAATGAATCCTTT | 29979 |
rs761808572 | snp | C/T | 1.65721e-05 | 0.0028785 | missense | UBQLN1 | GRCh38.p7 | 9:83677748 | CTCCAGGCACCAAAT[C/T]TGGCGCAGTAGTACT | 29979 |
rs761858174 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83695435 | GAACTCCTGACCTTG[C/T]GATCTGCCCACCTCA | 29979 |
rs761874313 | snp | A/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83680788 | TTGAACCTGAGGAGG[A/T]GGTCAGGGGAACCCC | 29979 |
rs761915868 | snp | A/C | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83688273 | AATCCTATTTCAGAC[A/C]CAGAAAAAGAGGTTA | 29979 |
rs761937696 | snp | A/G | | | downstream-variant-500B | UBQLN1 | GRCh38.p7 | 9:83659631 | AAAAACCATACCACT[A/G]CAGTAGCTTAAAGGT | 29979 |
rs762110289 | snp | A/G | 1.64947e-05 | 0.00287177 | missense | UBQLN1 | GRCh38.p7 | 9:83664020 | CCTCCAGTGCTTCCT[A/G]ATGCCCCCAAGCCAG | 29979 |
rs762159957 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83689264 | CATCCCTTTCTATGG[C/T]CAAATAGTATGCCAT | 29979 |
rs762167613 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83686893 | CATTAAGTATATAAG[A/G]CAAATATCCCAAAAT | 29979 |
rs762196173 | snp | C/T | 1.64857e-05 | 0.00287099 | synonymous-codon, intron-variant | UBQLN1 | GRCh38.p7 | 9:83666371 | GAGGAAAGTTGGGAG[C/T]TGTTGTCTCATTTGT | 29979 |
rs762197943 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83707358 | CAAACCCACGAACTT[A/G]GGTGTGATCTAATTT | 29979 |
rs762210687 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83666729 | CCTTGAACAAACGTG[A/G]ATATATGCCATTGAA | 29979 |
rs762262093 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83689368 | CTATTATAAACAATG[C/T]GATACATTTATCTCA | 29979 |
rs762264506 | snp | A/G | 1.67164e-05 | 0.00289101 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83678635 | AAAAGAAAAAAAAAA[A/G]GCATTGAAATACACA | 29979 |
rs762288079 | snp | A/C | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83695664 | ACATCTATATGGCAG[A/C]TGCTTAACCAGTAAA | 29979 |
rs762296349 | snp | A/G | | | intron-variant, downstream-variant-500B | UBQLN1 | GRCh38.p7 | 9:83667455 | CCCCAATTCTTGCAA[A/G]GTGATCTTTTAGTTA | 29979 |
rs762387976 | snp | C/T | 1.64773e-05 | 0.00287026 | missense | UBQLN1 | GRCh38.p7 | 9:83677825 | GTGCTGGCAGTGCCG[C/T]TGGAAGCTGATGAAC | 29979 |
rs762407755 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83694702 | TACTTCCTTCTATTG[C/T]AAAAACTTAAAACTC | 29979 |
rs762494390 | in-del | -/A | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83673547 | GAGACTCGGTCTTTT[-/A]AAAAAAAAAAAAAAA | 29979 |
rs762509825 | snp | A/G | | | intron-variant, downstream-variant-500B | UBQLN1 | GRCh38.p7 | 9:83667414 | CCGTATTTAAGAGCA[A/G]TGTAAATGCTGGTAG | 29979 |
rs762564039 | snp | C/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83702859 | AATTTGACTCAATAC[C/G]TTTAAATTATGTCTA | 29979 |
rs762583814 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83683699 | AAGCCAATGACCAGT[C/T]ACACCCACAAAGCTT | 29979 |
rs762600218 | snp | C/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83672961 | TCAAGGCCAGGCATG[C/G]TGGTTCACACCTGTA | 29979 |
rs762719741 | snp | C/T | 1.67593e-05 | 0.00289471 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83663847 | CAACATTAAGGAATA[C/T]AAAACTTGAATGGAA | 29979 |
rs762769384 | in-del | -/TACAAT | 1.69885e-05 | 0.00291444 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83669168 | CACAGTCTTTTTCAA[-/TACAAT]TACAAACTCACCTGT | 29979 |
rs762769839 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83689472 | CTAATTGAGCATACA[C/T]AGATCACCAAACCCA | 29979 |
rs762778623 | snp | C/T | | | utr-variant-3-prime | UBQLN1 | GRCh38.p7 | 9:83661155 | TTTGCTGGGAGATGT[C/T]TGTCAAAGATGCTGT | 29979 |
rs762807463 | snp | A/G | 1.64885e-05 | 0.00287123 | missense | UBQLN1 | GRCh38.p7 | 9:83661800 | TGCTATGATGGCTGG[A/G]AGCCCAGTAACCTTT | 29979 |
rs762859045 | snp | A/T | 1.6492e-05 | 0.00287154 | synonymous-codon | UBQLN1 | GRCh38.p7 | 9:83682973 | AAAAGGGTTGCTAGT[A/T]GCAGAACCAGATGTA | 29979 |
rs762879940 | snp | C/T | 1.65004e-05 | 0.00287227 | synonymous-codon | UBQLN1 | GRCh38.p7 | 9:83677923 | ACCTTCACCAGAGGA[C/T]GTATTGCTCACCAAG | 29979 |
rs762914939 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83702281 | TAAAATGGTGAACTG[C/T]ATGGTAGGCAAATTA | 29979 |
rs762961277 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83669753 | AGAAGTAAGCCTTCA[C/T]GCCCAAGGCAACAAA | 29979 |
rs762970453 | in-del | -/T | 1.80039e-05 | 0.00300027 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83680082 | ATCAAAGTCAGAAAA[-/T]TTATCATTAACATGA | 29979 |
rs763031983 | snp | G/T | | | missense | UBQLN1 | GRCh38.p7 | 9:83663936 | TGCTGATGTCCAGGT[G/T]CAGTGGTTCCTGCTG | 29979 |
rs763051013 | snp | C/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83698777 | AAGTAGCCAAGCATG[C/G]TGATGTGAGCTTGCA | 29979 |
rs763199553 | snp | A/G | 3.30978e-05 | 0.0040679 | missense | UBQLN1 | GRCh38.p7 | 9:83669261 | GACAACATGTTTTGC[A/G]TCAGTTGTGGGTTTT | 29979 |
rs763201854 | snp | A/T | 1.76157e-05 | 0.00296775 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83664996 | GAGAAAGTAACCATT[A/T]TACACTTTCATTATC | 29979 |
rs763209203 | snp | A/G | | | downstream-variant-500B | UBQLN1 | GRCh38.p7 | 9:83659508 | ACAATTTAAGCCTAC[A/G]GTATTTTAAACATCC | 29979 |
rs763238469 | in-del | -/A | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83681887 | TAATACAGCAGAATG[-/A]AAAAATGACTTTCAT | 29979 |
rs763309285 | snp | C/G | | | intron-variant, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83706778 | CAACATCGCTATCGC[C/G]CCTCTAAAATCAAAC | 29979 |
rs763327729 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83686682 | TCTATCTTCAGTCCT[A/G]TTCCTTTCTTTCTAG | 29979 |
rs763411179 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83666524 | CCCCCAAGTGCCTCA[A/G]CTGGCACTTAAAAGG | 29979 |
rs763436448 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83676289 | AAATATTAACATGAA[A/G]TGTTAAAGTATCAAA | 29979 |
rs763460645 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83706101 | AATGGCAACCATATG[C/T]ATTTCACTGCTGCCA | 29979 |
rs763484239 | snp | C/T | | | intron-variant, downstream-variant-500B | UBQLN1 | GRCh38.p7 | 9:83667400 | CCTCAAGAAGTTAAC[C/T]GTATTTAAGAGCAAT | 29979 |
rs763515754 | snp | C/T | 1.68176e-05 | 0.00289974 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83678647 | AAAGGCATTGAAATA[C/T]ACATGAATTACATTA | 29979 |
rs763528099 | snp | C/G | 3.38685e-05 | 0.00411498 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83685956 | TTACTTTTAGAAGTA[C/G]GAACATTTATCCACA | 29979 |
rs763631156 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83703007 | AGTCTATGAAATCCC[A/G]GAATAAGCTAATTAG | 29979 |
rs763636056 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83682868 | GTGACATAATGTTTT[A/G]TTTTCTCATTTTATC | 29979 |
rs763642916 | snp | C/T | 1.65081e-05 | 0.00287293 | synonymous-codon | UBQLN1 | GRCh38.p7 | 9:83678459 | CTCTTGTGCAGCACT[C/T]AGCATTGGTTCCTGA | 29979 |
rs763643269 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83671884 | GATATCTTCTTCCAA[C/T]AGAAGGCTGTTTTTC | 29979 |
rs763814224 | snp | C/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83673041 | GTTCAAGCAGCCTGG[C/G]CAACATGGCGAAACC | 29979 |
rs763820056 | snp | C/T | 1.6607e-05 | 0.00288153 | missense | UBQLN1 | GRCh38.p7 | 9:83677742 | CTCCTACTCCAGGCA[C/T]CAAATTTGGCGCAGT | 29979 |
rs763845401 | snp | C/T | | | utr-variant-3-prime | UBQLN1 | GRCh38.p7 | 9:83661341 | AAATTATCAGTAGTA[C/T]AAATCTTACAGCATT | 29979 |
rs763858349 | snp | G/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83702731 | ACTTAACCACATGTG[G/T]GTGATGGTATCAAAG | 29979 |
rs763880196 | snp | A/G | 1.64806e-05 | 0.00287054 | missense | UBQLN1 | GRCh38.p7 | 9:83664003 | CATTAGTTCCCGAAG[A/G]GCCTCCAGTGCTTCC | 29979 |
rs763902059 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83662821 | GCTCACGCCTGTAAT[C/T]CCAGCACTTTGGGAG | 29979 |
rs763958923 | in-del | -/TT | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83693443 | TCTCAAGGTATCTTG[-/TT]TATCTGCCTTTTTCT | 29979 |
rs763962957 | snp | A/C/T | 2.32669e-05 | 0.00341071 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83677676 | TAAACAATGTTTTAA[A/C/T]TATGTAAATGAGGAC | 29979 |
rs763970472 | snp | A/G | 3.31246e-05 | 0.00406955 | synonymous-codon | UBQLN1 | GRCh38.p7 | 9:83669278 | CAGTTGTGGGTTTTC[A/G]GTTATTTGTTGCAAC | 29979 |
rs763983675 | in-del | -/TTAT | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83672050 | TTTCCTTAAACATAA[-/TTAT]GCCAGTCAACCTCAG | 29979 |
rs763992796 | in-del | -/A | 1.81889e-05 | 0.00301565 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83669344 | TGAAAGTTTGTTTTT[-/A]AAAAAGACATATTAA | 29979 |
rs763997457 | snp | A/T | 1.95166e-05 | 0.00312376 | missense | UBQLN1 | GRCh38.p7 | 9:83686127 | TGGTCAGTATGTGAT[A/T]TAAAACGTTTAGAGA | 29979 |
rs764018683 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83689667 | TTGATCAATTGGAAA[A/G]GATGACCTAAGTGGG | 29979 |
rs764025915 | snp | A/C/G | 6.59408e-05 | 0.00574168 | synonymous-codon, intron-variant | UBQLN1 | GRCh38.p7 | 9:83666368 | TTGGAGGAAAGTTGG[A/C/G]AGCTGTTGTCTCATT | 29979 |
rs764192720 | in-del | -/T | 1.68485e-05 | 0.00290241 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83682911 | GAAGGGAAAGGAGTA[-/T]TTTTTTCCCATCCCT | 29979 |
rs764268087 | snp | A/G | | | downstream-variant-500B | UBQLN1 | GRCh38.p7 | 9:83659534 | CATCCTTTAAGTGCT[A/G]ATAAGAATTTTAAGT | 29979 |
rs764292111 | in-del | -/C | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83680741 | TAAACATAAGTGTTT[-/C]CCTTGAGTTCTAGGT | 29979 |
rs764297684 | snp | C/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83698806 | CAGTCCCAGCTACTT[C/G]GGGGGCTAAGGCAGG | 29979 |
rs764303558 | snp | C/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83674729 | TAAGTTCTTGATAAG[C/G]TGACAGATGTTACTG | 29979 |
rs764352442 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83684609 | CTGAGTTCAGGAGTT[C/T]GTGACCAGCCTGGCC | 29979 |
rs764391081 | snp | A/C | 1.75616e-05 | 0.00296319 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83680071 | AAAACATACAAATCA[A/C]AGTCAGAAAATTTAT | 29979 |
rs764409808 | snp | C/G/T | 3.29724e-05 | 0.00406021 | synonymous-codon | UBQLN1 | GRCh38.p7 | 9:83665125 | GTTTGACATTGCTGA[C/G/T]AGTGTATCAGGATTC | 29979 |
rs764444397 | snp | A/G | 1.65064e-05 | 0.00287279 | missense | UBQLN1 | GRCh38.p7 | 9:83682963 | TACCTAAACCAAAAG[A/G]GTTGCTAGTAGCAGA | 29979 |
rs764446127 | snp | A/C | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83675273 | CCACTACCCTGCCAA[A/C]CCTCCAACAACCAAA | 29979 |
rs764453039 | snp | C/G | 1.79329e-05 | 0.00299435 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83677985 | AAAGACATAAAAAAT[C/G]ACAAAGAATAAGCTT | 29979 |
rs764477803 | snp | C/G | 9.84979e-05 | 0.00701707 | missense, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83707660 | CCCGGAGGACCGCCG[C/G]TTTCACCACTCTCGG | 29979 |
rs764499131 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83705145 | AATATCAAAATGTTA[A/G]CAGGGATATGGAGCA | 29979 |
rs764591779 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83706172 | GGCAAATAAGTTCAC[A/G]ATGCTGAAGTGACAT | 29979 |
rs764619977 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83686663 | ATAATCCATTCCTCA[A/G]ACTTCTATCTTCAGT | 29979 |
rs764664401 | snp | C/T | 1.69622e-05 | 0.00291219 | missense | UBQLN1 | GRCh38.p7 | 9:83669320 | TCCTGGTGTGTTGAA[C/T]ATACTAGCTGAAAGT | 29979 |
rs764691849 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83666555 | GAGGAAGGTAGAACA[C/T]AAATAAAAAAAGGAA | 29979 |
rs764735825 | snp | A/C | 7.86859e-05 | 0.0062719 | missense, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83707518 | CTGGACGGAGCTATT[A/C]TCGGGCACGGCGAAT | 29979 |
rs764790235 | snp | A/G | 1.79081e-05 | 0.00299228 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83664987 | AAATTCTCAGAGAAA[A/G]TAACCATTATACACT | 29979 |
rs764818603 | snp | A/G | 2.17252e-05 | 0.00329577 | synonymous-codon | UBQLN1 | GRCh38.p7 | 9:83686141 | TTTAAAACGTTTAGA[A/G]ATTTCTTCCTTAAAC | 29979 |
rs764833077 | snp | A/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83698145 | ATCATGCCTGCAATA[A/T]ATATTGGCCATTATG | 29979 |
rs765146934 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83699948 | AGCCAGTTTAATAAC[A/G]GTATCTTGAAATCTG | 29979 |
rs765148115 | snp | C/G | 4.96841e-05 | 0.00498393 | missense | UBQLN1 | GRCh38.p7 | 9:83677751 | CAGGCACCAAATTTG[C/G]CGCAGTAGTACTCTG | 29979 |
rs765173855 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83671669 | CATCCAGGCTTTTTT[C/T]CTTTTTTTCTTTTTT | 29979 |
rs765177883 | snp | C/T | | | downstream-variant-500B | UBQLN1 | GRCh38.p7 | 9:83659803 | TGTGCTATCTTTTTA[C/T]CACACCACAAAAGAC | 29979 |
rs765182554 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83689395 | CTCAGAGAAACTGAC[A/G]GACTAAATGGGCAAA | 29979 |
rs765188165 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83677295 | TGACCAGGTGCAGCG[A/G]CTCACACCTATAATC | 29979 |
rs765188680 | snp | A/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83676624 | ATCCACTGTATTCTA[A/T]AAAAGAATATATATC | 29979 |
rs765199484 | snp | A/G | | | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83708006 | CGCGGAGCACGCCGG[A/G]TAACGCGCCTGGCGG | 29979 |
rs765200208 | in-del | -/TA | 1.64894e-05 | 0.00287131 | frameshift-variant, intron-variant | UBQLN1 | GRCh38.p7 | 9:83666420 | CAGCAAATAGGGGAT[-/TA]TATTCAGCATCATCT | 29979 |
rs765223674 | in-del | -/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83674183 | AAAATCACTGCAGCA[-/T]TTAAAAAAAAAAAAA | 29979 |
rs765248784 | in-del | -/GGCGGC | 0.000273168 | 0.0116837 | utr-variant-5-prime, upstream-variant-2KB, cds-indel | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83707686 | CTCGGCCATGGCTGT[-/GGCGGC]GGCGGCGGCGGTGAC | 29979 |
rs765378376 | in-del | -/AAAAC | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83677570 | CTATCTCAAAAAAAC[-/AAAAC]AAAACAAAACAAAAC | 29979 |
rs765414129 | snp | C/T | | | upstream-variant-2KB, intron-variant | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83708683 | CGATCAGTCAGGCAA[C/T]CTGTATTGACAGTGG | 29979 |
rs765470919 | snp | C/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83696170 | GTCTCAAACTCTTGA[C/G]CTCATAATCCGCCTG | 29979 |
rs765546485 | snp | C/T | 3.2969e-05 | 0.00405998 | synonymous-codon, intron-variant | UBQLN1 | GRCh38.p7 | 9:83666374 | GAAAGTTGGGAGCTG[C/T]TGTCTCATTTGTTCT | 29979 |
rs765582215 | snp | C/T | 1.64963e-05 | 0.00287192 | synonymous-codon | UBQLN1 | GRCh38.p7 | 9:83664022 | TCCAGTGCTTCCTAA[C/T]GCCCCCAAGCCAGGA | 29979 |
rs765593628 | snp | A/G | 1.6549e-05 | 0.0028765 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83666475 | TAACTGGAAATATCT[A/G]AAACAAGTAATGTAC | 29979 |
rs765653001 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83664582 | AAGAGCAAAAACCGA[C/T]CTCTTAATAAATAAA | 29979 |
rs765667428 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83704001 | GTGTTAAGGAATCTA[C/T]ATTACATAGAAATAC | 29979 |
rs765686016 | snp | A/C | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83663333 | ATTATTAGTAAAACC[A/C]ATGTATGTTTGTAGA | 29979 |
rs765737864 | snp | A/C | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83686638 | ACAGTTAGCTCTTAC[A/C]ACGTCCAAAATAATC | 29979 |
rs765762434 | snp | G/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83675117 | ACTTAACCAGTCAAC[G/T]TCATGAATTTTTATT | 29979 |
rs765779134 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83665380 | AAGCCATTTCCATAA[C/T]GGAAGAAAATCAGGA | 29979 |
rs765823034 | snp | A/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83664297 | GCTGGTGCACACCTG[A/T]AGTATCAGTTACTTG | 29979 |
rs765854569 | snp | C/T | 1.6477e-05 | 0.00287024 | missense | UBQLN1 | GRCh38.p7 | 9:83677826 | TGCTGGCAGTGCCGC[C/T]GGAAGCTGATGAACT | 29979 |
rs765855817 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83662715 | CCAGAAACTATGCTA[C/T]GCTAGCTTATCAGGA | 29979 |
rs765942953 | in-del | -/C | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83665355 | GACCTCCTCCTAAGT[-/C]CCATCATGAAAGCCA | 29979 |
rs766069312 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83692045 | TCTGAGTAAAAAATA[C/T]ACAAAACTTGGAACA | 29979 |
rs766099145 | in-del | -/AAAAAC | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83673563 | AAAAAAAAAAAAAAA[-/AAAAAC]AAAAAAAAAAAACTG | 29979 |
rs766163441 | snp | A/G | 0.000113263 | 0.00752454 | missense, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83707627 | GCACCTTCGGCTCCG[A/G]CGGCGCTATCCTGGG | 29979 |
rs766201012 | in-del | -/AATC | | | upstream-variant-2KB, intron-variant | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83709000 | AACCAGCCCATTATT[-/AATC]AATGTTGCACAATTT | 29979 |
rs766237196 | snp | G/T | | | downstream-variant-500B | UBQLN1 | GRCh38.p7 | 9:83659667 | AGAGCTTATCGCCCA[G/T]TCCAGCACACCTATA | 29979 |
rs766245627 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83686887 | CTGAACCATTAAGTA[C/T]ATAAGGCAAATATCC | 29979 |
rs766250228 | in-del | -/TACC | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83703895 | AATAGGAAAATAAAT[-/TACC]TACCACCTTACAATT | 29979 |
rs766272209 | snp | C/T | 3.34264e-05 | 0.00408804 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83663852 | TTAAGGAATACAAAA[C/T]TTGAATGGAAAAGAA | 29979 |
rs766323798 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83681880 | TAGAGCTATAATACA[A/G]CAGAATGAAAAATGA | 29979 |
rs766332366 | snp | A/G | 3.29761e-05 | 0.00406041 | synonymous-codon | UBQLN1 | GRCh38.p7 | 9:83661802 | CTATGATGGCTGGGA[A/G]CCCAGTAACCTTTCA | 29979 |
rs766455159 | snp | A/G | | | intron-variant, utr-variant-3-prime | UBQLN1 | GRCh38.p7 | 9:83667783 | TTTTTACACTCAAGA[A/G]TCTTTTTAAATATTT | 29979 |
rs766459859 | in-del | -/A | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83683414 | GCGAGACTCCGTCTC[-/A]AAAAAAAAAAAAAAA | 29979 |
rs766517845 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83668849 | CATTGCTCTTAATTG[C/T]TTTCAAGATTTACAT | 29979 |
rs766627294 | snp | A/C | | | intron-variant, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83706405 | AAAACAAAAGTGATA[A/C]TTCTGTTGGTGGTAA | 29979 |
rs766657761 | in-del | -/GGCGCCAGCACCTTCGGCTCCGGC | 3.59292e-05 | 0.00423832 | cds-indel, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83707605 | GGCAGCGGCCGCGGG[-/GGCGCCAGCACCTTCGGCTCCGGC]GGCGCTATCCTGGGA | 29979 |
rs766680761 | snp | C/T | 1.64855e-05 | 0.00287097 | synonymous-codon | UBQLN1 | GRCh38.p7 | 9:83665068 | CGTTGCTAATGTCTG[C/T]AAACCCTGCTGAATC | 29979 |
rs766691722 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83683864 | CTATCTCTACTAAAA[C/T]ACAAAAATTAGCCGG | 29979 |
rs766725519 | in-del | -/GT | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83662244 | CATGCAGAAAAACCT[-/GT]ATGTGTGTGTGTATA | 29979 |
rs766745958 | in-del | -/AGTGCCACTGGCAGTACTACCAGT | 0.000148484 | 0.00861511 | cds-indel | UBQLN1 | GRCh38.p7 | 9:83677772 | AGTACTCTGCCCAGA[-/AGTGCCACTGGCAGTACTACCAGT]AGTGCCACTGGCAGT | 29979 |
rs766841414 | in-del | -/C | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83682140 | ATACAAAAAAATTAG[-/C]CGGGCGTAGTGGCAC | 29979 |
rs766856827 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83673218 | CTGGGCGACGACTCT[A/G]TCTCAAACAAAACAA | 29979 |
rs766891839 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83697168 | CCCAAGTTTGTACTG[A/G]GTTTGAATCTACAGT | 29979 |
rs766894787 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83685256 | ATCCTGGAGAAAATA[C/T]TGGAGAGCTCTTTTA | 29979 |
rs766983358 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83681932 | GAGGGACTATATGGA[C/T]GGGCACCTTACAAAC | 29979 |
rs767002643 | snp | A/G/T | 0.00019871 | 0.00996583 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83663865 | AACTTGAATGGAAAA[A/G/T]AACTGATACCTGAGG | 29979 |
rs767073341 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83679249 | GAAATGACCCATCTG[C/T]TTTTTGTTCGTTTTT | 29979 |
rs767115655 | snp | A/C | 1.64795e-05 | 0.00287045 | missense | UBQLN1 | GRCh38.p7 | 9:83661913 | TTGTTCCAGTTGTTG[A/C]TGAAATCTGACTTCT | 29979 |
rs767152867 | snp | G/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83673758 | TACAAAAGCAGTGAG[G/T]ACTTGCAACAGAAAC | 29979 |
rs767208832 | snp | A/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83702956 | TGCCTGAACATTTCA[A/T]GTAAATGTACTTCAA | 29979 |
rs767263817 | snp | C/G | 3.29533e-05 | 0.00405901 | missense | UBQLN1 | GRCh38.p7 | 9:83677842 | GGAAGCTGATGAACT[C/G]TGGGAAGTCTGTGGA | 29979 |
rs767293573 | in-del | -/GC/GTGA | | | upstream-variant-2KB, intron-variant | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83709617 | TGTGTGTGTGTGTGT[-/GC/GTGA]GTGTCTGTCTCCCTG | 29979 |
rs767304872 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83690974 | AAAACCCCGTCTCTG[C/T]TAAAAATACAAAAAT | 29979 |
rs767321214 | in-del | -/C | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83665772 | ACCAGTTTCAAAACA[-/C]CCAAGACTGACTTCT | 29979 |
rs767340759 | snp | C/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83680811 | GGAACCCCCAACTTA[C/G]AGCTGGTCAGTCAGA | 29979 |
rs767359191 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83669783 | AAGATGTAATGCCTC[C/T]ACCCATTTTCACTGT | 29979 |
rs767387875 | snp | C/G | 1.68071e-05 | 0.00289884 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83683103 | AGAGTAAGCAGTAGA[C/G]CTGATTATTTTTAAA | 29979 |
rs767456272 | snp | C/G/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83691840 | ATGAATTTATGGCAC[C/G/T]TCATGCTAAAAGTTG | 29979 |
rs767464742 | snp | A/T | 1.64792e-05 | 0.00287042 | synonymous-codon | UBQLN1 | GRCh38.p7 | 9:83683006 | GTTACTATTAGGAGT[A/T]GATGATGTAGTAACA | 29979 |
rs767638815 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83677419 | AATACAAAATTAGCC[A/G]GGCATGGTGGCAGGT | 29979 |
rs767673309 | snp | C/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83688312 | TCCCTTCCCCTCACA[C/G]TGATACAGCTAATAA | 29979 |
rs767685358 | snp | C/T | | | upstream-variant-2KB, intron-variant | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83708825 | GAGGTGTTCGCCTTA[C/T]ATTCTATCAAATTAA | 29979 |
rs767736565 | snp | A/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83705427 | GCTAAGTTTTGTATT[A/T]TTAGTAGAGACGGGG | 29979 |
rs767753674 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83706358 | GAAAATACAAAAATG[A/G]TAAGGAAAATTTTTA | 29979 |
rs767763112 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83676496 | CCTCTCAAAAGATTG[C/T]TAGTATCAAAGTAAG | 29979 |
rs767798824 | in-del | -/A | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83698912 | AGTGAGACCTGTCTC[-/A]AAAAAAAAAAAAAAA | 29979 |
rs767928636 | snp | A/C/G | 0.000262318 | 0.0114495 | missense, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83707649 | TATCCTGGGAGCCCG[A/C/G]AGGACCGCCGCTTTC | 29979 |
rs767950755 | snp | A/C/G | 4.94401e-05 | 0.00497168 | missense | UBQLN1 | GRCh38.p7 | 9:83683031 | GTAACATTGCTTCCA[A/C/G]CTGTATTTGTTTGCT | 29979 |
rs768005512 | snp | C/G | 1.6473e-05 | 0.00286988 | missense | UBQLN1 | GRCh38.p7 | 9:83679922 | GGGATTTTCCATGAT[C/G]TGGACCATCATTTCA | 29979 |
rs768013275 | snp | A/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83695926 | TGGTATTTGTATAGT[A/T]TCACTTCACTTTTCA | 29979 |
rs768040808 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83683782 | AATCCCAGCACTTTG[C/T]GAGGCCGAGGCAGGC | 29979 |
rs768054934 | snp | A/G | 3.29772e-05 | 0.00406048 | missense, intron-variant | UBQLN1 | GRCh38.p7 | 9:83666358 | TACTCACTTGTTGGA[A/G]GAAAGTTGGGAGCTG | 29979 |
rs768077300 | in-del | -/CA | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83689006 | GGTTTCTGGAGTATT[-/CA]CAGACATGTGTTACA | 29979 |
rs768190141 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83695518 | TTTTATACTTTTCAA[C/T]ATCATTTGAATTTCT | 29979 |
rs768237244 | snp | C/T | 8.40569e-05 | 0.00648239 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83664082 | TATCCTAAGGTCCTG[C/T]AAAACCAGAAGCCAG | 29979 |
rs768249355 | snp | G/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83704099 | TATCCTCTGGAGGTC[G/T]TCGGCTTACCCTCTG | 29979 |
rs768288422 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83669038 | TGCAAAGAAACACAC[A/G]GTCTAAAAAATTGGA | 29979 |
rs768288541 | snp | A/G | 3.29821e-05 | 0.00406078 | missense | UBQLN1 | GRCh38.p7 | 9:83665054 | AGGCCCGGGGCTTCC[A/G]TTGCTAATGTCTGTA | 29979 |
rs768380142 | snp | A/G | 3.62957e-05 | 0.00425987 | synonymous-codon, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83707605 | GGCAGCGGCCGCGGG[A/G]GCGCCAGCACCTTCG | 29979 |
rs768596270 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83676428 | TTAACCAGTCAGGAA[A/G]TATGATTAAATCTTT | 29979 |
rs768599897 | snp | C/T | | | utr-variant-3-prime | UBQLN1 | GRCh38.p7 | 9:83660772 | TTGGCTCACAACTCA[C/T]TTTAAATTTGTGTAT | 29979 |
rs768609696 | snp | A/C | 2.41905e-05 | 0.00347774 | intron-variant, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83707491 | GGCCCGAGCCCCAGG[A/C]GGCCTCACCTGCTGG | 29979 |
rs768673432 | snp | G/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83691787 | TCCTCCAACCTCATG[G/T]AACTCTTGGTTCTGG | 29979 |
rs768729081 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83671262 | AACTCCTGTTCATGT[C/T]GATATTTTGACATCC | 29979 |
rs768732539 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83670513 | GTTTGCATGATACTG[C/T]AGTCTATTAAGTATG | 29979 |
rs768801290 | snp | C/G | 1.65356e-05 | 0.00287533 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83683070 | TGATCCTGAGGCCTA[C/G]GGAAAATAATTAATC | 29979 |
rs768913976 | in-del | -/AT | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83662264 | TGTGTGTGTATATAC[-/AT]ATACATATACACACA | 29979 |
rs768920236 | snp | C/T | 1.64749e-05 | 0.00287005 | missense | UBQLN1 | GRCh38.p7 | 9:83663961 | CTGCTGTGGGACTTG[C/T]GTTTTCACTAGGTGT | 29979 |
rs768957650 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83700749 | AGTATTAACAGGTCA[A/G]GGAACTAGAAGGTCA | 29979 |
rs769142107 | snp | C/G | 4.95651e-05 | 0.00497796 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83666320 | CAAGCAAATCATTAC[C/G]CAAGATAGCTAACAT | 29979 |
rs769172208 | in-del | -/A | 0.00699132 | 0.0587093 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83661949 | CTGTAGCTATTAAAG[-/A]AAAAAAAAATTAATC | 29979 |
rs769204636 | snp | C/T | 1.65378e-05 | 0.00287552 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83666472 | TTTTAACTGGAAATA[C/T]CTGAAACAAGTAATG | 29979 |
rs769219588 | in-del | -/G | 1.74488e-05 | 0.00295366 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83680068 | CAAAAACATACAAAT[-/G]CAAAGTCAGAAAATT | 29979 |
rs769277452 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83677306 | AGCGGCTCACACCTA[C/T]AATCCCAGCAATTTG | 29979 |
rs769300903 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83676944 | GAGTTCAGTCTACAG[A/G]AAAGTGGACAAAAGT | 29979 |
rs769333610 | snp | C/T | | | intron-variant, downstream-variant-500B | UBQLN1 | GRCh38.p7 | 9:83667288 | TCAAAAGACACATTT[C/T]ATATCATTTTCCCCA | 29979 |
rs769340965 | in-del | -/TC/TGTC | | | upstream-variant-2KB, intron-variant | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83709622 | GTGTGTGTGTGTGTC[-/TC/TGTC]TGTCTCCCTGCATTT | 29979 |
rs769349912 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83689142 | TTTCTGTTTCCATAC[A/G]AGTATTTCATATAAA | 29979 |
rs769359829 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83705898 | GGGATCCCATTTAAT[A/G]TTAAGTTCTAAAACA | 29979 |
rs769366082 | in-del | -/C | | | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83707966 | TCCTCCCTGCCCCTT[-/C]CCCCACGTCCCTTCG | 29979 |
rs769482423 | snp | C/T | 1.68032e-05 | 0.0028985 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83682919 | AAGGAGTATTTTTTC[C/T]CATCCCTACTGGAAT | 29979 |
rs769526991 | snp | A/G | 1.6492e-05 | 0.00287154 | synonymous-codon | UBQLN1 | GRCh38.p7 | 9:83677917 | TTGACTACCTTCACC[A/G]GAGGATGTATTGCTC | 29979 |
rs769530088 | snp | G/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83683356 | GGCGGAGCTTGCAGT[G/T]AGCGAGATCGCGCCA | 29979 |
rs769546306 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83702163 | GGGCCCAGGGAGAAA[C/T]GAAGGGCAACTGCTA | 29979 |
rs769579173 | snp | A/C | 1.68357e-05 | 0.00290131 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83678399 | TATTTGTGTTAAAAC[A/C]GAAGCTACTCCTTGG | 29979 |
rs769611677 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83703818 | CAAATGTATATAGCA[C/T]TGTAAAAAATTAAGG | 29979 |
rs769766857 | snp | C/T | 1.64784e-05 | 0.00287035 | missense | UBQLN1 | GRCh38.p7 | 9:83677820 | CCACAGTGCTGGCAG[C/T]GCCGCTGGAAGCTGA | 29979 |
rs769768092 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83684681 | CCGGGCGTGGTGGCG[C/T]ATGCCTGTAATTCCA | 29979 |
rs769792540 | snp | C/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83702173 | AGAAACGAAGGGCAA[C/G]TGCTAAAGGGTACAG | 29979 |
rs769814855 | snp | A/G | 0.00105913 | 0.0229879 | utr-variant-5-prime, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83707715 | CGGTGACTCAGGCAA[A/G]CAGGAGGGAGCAGGC | 29979 |
rs769817566 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83692847 | ACAAGAGCGGAACTC[C/T]GTTTTAAAAATAATA | 29979 |
rs769838464 | snp | A/C | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83699799 | GGCTCTACCAGCCAC[A/C]TGGTCTATTCTGAAA | 29979 |
rs769866759 | snp | A/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83662731 | GCTAGCTTATCAGGA[A/T]TACAGATATGTATGA | 29979 |
rs769871912 | snp | A/C | 3.65785e-05 | 0.00427643 | intron-variant, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83707460 | CGGGCGGAGGTCCTG[A/C]CGCCACCCCCATCCC | 29979 |
rs769907301 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83681499 | AACCCAAGTGGAATG[A/G]CTACTTTCAGAAGAA | 29979 |
rs769952869 | snp | A/G | 6.65956e-05 | 0.00577004 | missense | UBQLN1 | GRCh38.p7 | 9:83686067 | CCATGCTGACTCAAG[A/G]TATCTTGATCTTTCA | 29979 |
rs769987155 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83678383 | CCCTCAATCATACAC[A/G]TATTTGTGTTAAAAC | 29979 |
rs770015483 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83670466 | AAAGCAAGTCACACA[C/T]ATTTTTTGGTTTCCC | 29979 |
rs770188193 | in-del | -/ACATATACAC | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83662268 | TGTGTATATACATAT[-/ACATATACAC]ACACACACACACACA | 29979 |
rs770210873 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83676220 | AATATGCTGACAATC[C/T]GATAGGCCAGCAGAG | 29979 |
rs770255069 | snp | A/T | | | upstream-variant-2KB, nc-transcript-variant | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83708308 | CCTGCGCGCTTGCTG[A/T]CCAGGTAGTCTCCCC | 29979 |
rs770263592 | snp | C/G | | | utr-variant-3-prime | UBQLN1 | GRCh38.p7 | 9:83660220 | GGACTGGTGGGTAAC[C/G]TGGCCTCTTAACCTT | 29979 |
rs770398918 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83674811 | ATTACCCTCTATAAA[C/T]AGTCTGAATGGAACA | 29979 |
rs770446059 | in-del | -/A | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83688912 | TTTCAAATACCTACC[-/A]AAAAAATAGTATTTT | 29979 |
rs770529065 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83664788 | GCTAGGTGTGGTGGT[A/G]CACACCTGTAGTCCC | 29979 |
rs770536613 | snp | C/G | | | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83707913 | GTGTGTTCAGGCGCC[C/G]CTCGCTCACACCGAC | 29979 |
rs770543416 | in-del | -/A | 1.67363e-05 | 0.00289272 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83678641 | AAAAAAAAGGCATTG[-/A]AAATACACATGAATT | 29979 |
rs770613960 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83675907 | AGTAGATACAAGGAA[A/G]ATATTGTAACTAAAT | 29979 |
rs770621039 | snp | G/T | 1.64909e-05 | 0.00287144 | missense, intron-variant | UBQLN1 | GRCh38.p7 | 9:83666423 | GCAAATAGGGGATTA[G/T]TCAGCATCATCTATG | 29979 |
rs770631316 | in-del | -/T | 1.77289e-05 | 0.00297727 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83664994 | CAGAGAAAGTAACCA[-/T]TATACACTTTCATTA | 29979 |
rs770672616 | snp | C/T | | | intron-variant, downstream-variant-500B | UBQLN1 | GRCh38.p7 | 9:83667117 | ATCTGGATTTCACCT[C/T]ACTACTACCAGAGAT | 29979 |
rs770682162 | in-del | -/TGTC | | | upstream-variant-2KB, intron-variant | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83709618 | GTGTGTGTGTGTGTG[-/TGTC]TGTCTGTCTCCCTGC | 29979 |
rs770720155 | snp | A/G | 8.23744e-05 | 0.0064172 | synonymous-codon | UBQLN1 | GRCh38.p7 | 9:83663980 | TTCACTAGGTGTGGC[A/G]TTAGATCCATTAGTT | 29979 |
rs770821163 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83699691 | GTAAAAATTTCCAAT[A/G]AGAAGTGTTTTGATG | 29979 |
rs770949251 | snp | C/T | 1.67739e-05 | 0.00289597 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83678415 | GAAGCTACTCCTTGG[C/T]CTGAACCTTGGAGCC | 29979 |
rs770994394 | snp | A/C | 1.64844e-05 | 0.00287087 | missense | UBQLN1 | GRCh38.p7 | 9:83677801 | GTACTACCAGTAGTG[A/C]CACCCACAGTGCTGG | 29979 |
rs771003133 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83671460 | GATCCATGGGCTGCA[C/T]GCAGAATGAATGCTG | 29979 |
rs771042840 | in-del | -/TTT | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83697734 | CTATTTTTTGTACCC[-/TTT]TTTTTTTTTTTTTTT | 29979 |
rs771096983 | snp | A/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83663869 | TGAATGGAAAAGAAC[A/T]GATACCTGAGGATTT | 29979 |
rs771130324 | snp | A/C | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83691695 | AAACCAAACCAAAGT[A/C]CTGACAGACACGTGA | 29979 |
rs771146726 | snp | C/T | | | missense | UBQLN1 | GRCh38.p7 | 9:83680020 | AGCTACTCAGACCTG[C/T]AAGTCCCCCAAGGCC | 29979 |
rs771236261 | snp | C/T | 1.66147e-05 | 0.0028822 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83682937 | TCCCTACTGGAATGA[C/T]TAAAGACACTTACCT | 29979 |
rs771240494 | snp | A/C | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83681390 | AAGACATCCTCAGAA[A/C]TCAATCTAGTAGGAA | 29979 |
rs771253351 | snp | A/G | | | stop-gained | UBQLN1 | GRCh38.p7 | 9:83677766 | GCGCAGTAGTACTCT[A/G]CCCAGAAGTGCCACT | 29979 |
rs771282385 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83669512 | TACATGCCCAACATA[C/T]ACCAGGAAAAGAGGA | 29979 |
rs771287654 | snp | C/T | 1.64999e-05 | 0.00287222 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83666340 | ATAGCTAACATCTTG[C/T]CTTACTCACTTGTTG | 29979 |
rs771303357 | snp | A/C | | | upstream-variant-2KB, intron-variant, nc-transcript-variant | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83708447 | CTGGTGATAAAATAG[A/C]GGCGAGGTATTTTGT | 29979 |
rs771465652 | snp | C/T | 1.64757e-05 | 0.00287012 | missense | UBQLN1 | GRCh38.p7 | 9:83679986 | TGTAGTTCAGAGAAG[C/T]TGGTAGTATTCAAAC | 29979 |
rs771563034 | in-del | -/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83675798 | CACTACATATCAGTA[-/T]TTAACAGATGAACTT | 29979 |
rs771616600 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83685053 | ACTGTTGTATCATAT[A/G]TAACGGGCTTAATTA | 29979 |
rs771618121 | in-del | -/TAT | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83669442 | ACAAATGATTATACA[-/TAT]TATGTATCAACTGAA | 29979 |
rs771662758 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83698589 | TTAAAATGTGGTACA[C/T]ACATATAATGGAATA | 29979 |
rs771665583 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83683482 | AAGGGTAAACTCTCA[A/G]ACCAAATCAAATTAT | 29979 |
rs771725026 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83674640 | CTCGGCTCTCAGGAG[A/G]AACAGTTTTTCTCAG | 29979 |
rs771812720 | snp | G/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83675758 | TTTTGGAATGAGTAC[G/T]TATTTTGAATAAGTC | 29979 |
rs771841039 | in-del | -/C | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83671185 | CTTCTACAGTCCCCT[-/C]CCTCCATAGAAGTCT | 29979 |
rs771861990 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83686310 | GGCAGGAGGACTGCC[C/T]GAGTCCAGGAGTTCG | 29979 |
rs771877740 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83703763 | TGGAAAAAAGCTTAA[A/G]CTTTATTAGTAACCT | 29979 |
rs771891656 | snp | C/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83664516 | CAACTACTGGGGAGG[C/G]TGAGGTGGGAGGATC | 29979 |
rs772020500 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83665814 | TTAAATAATAAAATA[C/T]CATGGCAATCTCAAG | 29979 |
rs772035273 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83704555 | CTGGGCCGGGTGCCC[A/G]GTGGTTCACACCTGT | 29979 |
rs772047091 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83681692 | AACTACAGTAGCAGA[C/T]AGCAGTGCTCACCAA | 29979 |
rs772097856 | in-del | -/AG | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83685367 | TTCGTATGTTATGCA[-/AG]AGTGATATGATAAAA | 29979 |
rs772131447 | snp | A/G | 1.96307e-05 | 0.00313289 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83678625 | TATTTCCAAAAAAAG[A/G]AAAAAAAAAGGCATT | 29979 |
rs772141712 | snp | C/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83694124 | TTTTAAACAACCATT[C/G]TCCATCTCACCTATT | 29979 |
rs772155197 | snp | C/T | 1.68741e-05 | 0.00290461 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83663824 | CTTTTTGGAAATTTC[C/T]AAATTTCCAACATTA | 29979 |
rs772156624 | snp | A/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83662406 | AATTCTAAAGCTTCA[A/T]TGATTCTTCGAATGA | 29979 |
rs772169070 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83689269 | CTTTCTATGGCCAAA[C/T]AGTATGCCATTGTAT | 29979 |
rs772236416 | snp | C/G | 5.08746e-05 | 0.00504328 | utr-variant-3-prime | UBQLN1 | GRCh38.p7 | 9:83661738 | TATTTTAAAGTTTAA[C/G]AGCCGTTATCAAAAA | 29979 |
rs772262109 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83680863 | GTGACCAGTATCTGA[A/G]GTAGGGGCAGTCTTG | 29979 |
rs772277169 | snp | A/C | 1.65061e-05 | 0.00287277 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83666444 | ATCATCTATGGGGCA[A/C]GTGTTCAAACAATTT | 29979 |
rs772280834 | snp | C/G | 1.64814e-05 | 0.00287061 | missense | UBQLN1 | GRCh38.p7 | 9:83677810 | GTAGTGCCACCCACA[C/G]TGCTGGCAGTGCCGC | 29979 |
rs772285212 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83690125 | CACTATTTAACAAAC[C/T]ACATGTCCACAAAAA | 29979 |
rs772312218 | snp | A/G | | | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83707939 | CCGACATCCGCAGCA[A/G]CCACCGCTTCCTCCT | 29979 |
rs772405514 | snp | C/T | | | upstream-variant-2KB, intron-variant, nc-transcript-variant | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83708390 | TCGCCTTGCCCTCCC[C/T]TGCCTCTCTGTCTAC | 29979 |
rs772454061 | in-del | -/GAATG | 1.66888e-05 | 0.00288862 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83663855 | AGGAATACAAAACTT[-/GAATG]GAAAAGAACTGATAC | 29979 |
rs772489178 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83696962 | CTTCTTAAAAAAAGA[C/T]ACAGAGTATTGCTAT | 29979 |
rs772493873 | snp | G/T | 1.65842e-05 | 0.00287955 | missense | UBQLN1 | GRCh38.p7 | 9:83669227 | TAGTGACTGCATCAT[G/T]CTTCTCATGTAGGGG | 29979 |
rs772497221 | snp | A/G | 1.64857e-05 | 0.00287099 | synonymous-codon | UBQLN1 | GRCh38.p7 | 9:83683048 | TGTATTTGTTTGCTG[A/G]GCTGAATGATCCTGA | 29979 |
rs772554482 | in-del | -/C | | | intron-variant, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83706213 | ATCTACTGATACGTG[-/C]CAACTTACTCTGAAT | 29979 |
rs772557473 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83692627 | GGAGGCCGAGGCAGG[C/T]GGATCACCTGAGGTC | 29979 |
rs772620583 | snp | C/T | 3.31422e-05 | 0.00407063 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83682944 | TGGAATGACTAAAGA[C/T]ACTTACCTAAACCAA | 29979 |
rs772642413 | in-del | -/GAGGGGTC | | | upstream-variant-2KB, intron-variant | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83708493 | AGCGTTTGATATTTG[-/GAGGGGTC]GTATTGCCCTATGCG | 29979 |
rs772673311 | snp | G/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83668705 | GCAGGGGAATCAATA[G/T]TTGAAAGAAGGAGAA | 29979 |
rs772784590 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83674797 | GAAGTGACCGGAAAA[C/T]TACCCTCTATAAATA | 29979 |
rs772788853 | in-del | -/CCCTGGGATGAGGCCCGGGGCTTCCGTTGCTAATGTCTGTAAAC | 1.65647e-05 | 0.00287786 | frameshift-variant | UBQLN1 | GRCh38.p7 | 9:83664042 | CAAGCCAGGAGTAAA[lengthTooLong]CCTACAGAAAGCACA | 29979 |
rs772831475 | snp | C/T | 3.93167e-05 | 0.0044336 | missense, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83707609 | GCGGCCGCGGGGGCG[C/T]CAGCACCTTCGGCTC | 29979 |
rs772868401 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83683565 | TAAAATAAAACCCTA[C/T]AAAATACAAAATATG | 29979 |
rs772870827 | snp | A/G | | | synonymous-codon | UBQLN1 | GRCh38.p7 | 9:83665035 | ATAAGCCTACCCTGG[A/G]ATGAGGCCCGGGGCT | 29979 |
rs772938709 | snp | C/G | 1.65149e-05 | 0.00287353 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83666324 | CAAATCATTACCCAA[C/G]ATAGCTAACATCTTG | 29979 |
rs772987126 | snp | A/G | 0.000179808 | 0.00948006 | utr-variant-5-prime, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83707723 | CAGGCAAGCAGGAGG[A/G]AGCAGGCGAGCAAGG | 29979 |
rs773011785 | snp | A/C | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83674801 | TGACCGGAAAATTAC[A/C]CTCTATAAATAGTCT | 29979 |
rs773032287 | snp | A/G | 1.64942e-05 | 0.00287173 | missense | UBQLN1 | GRCh38.p7 | 9:83677919 | GACTACCTTCACCAG[A/G]GGATGTATTGCTCAC | 29979 |
rs773055542 | snp | A/T | 3.35514e-05 | 0.00409568 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83663843 | TTTCCAACATTAAGG[A/T]ATACAAAACTTGAAT | 29979 |
rs773059112 | snp | A/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83704565 | TGCCCGGTGGTTCAC[A/T]CCTGTAATCCTAGCA | 29979 |
rs773061627 | snp | G/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83665915 | CGAGTTTGAGGAAAT[G/T]AGATCTACCCCTTGG | 29979 |
rs773143766 | snp | C/T | 1.64977e-05 | 0.00287203 | synonymous-codon | UBQLN1 | GRCh38.p7 | 9:83661790 | ACAGAAATGCTGCTA[C/T]GATGGCTGGGAGCCC | 29979 |
rs773146502 | snp | C/T | | | utr-variant-3-prime | UBQLN1 | GRCh38.p7 | 9:83660629 | GTTGCCAGTATTATT[C/T]AAGCTGGCCCCATCC | 29979 |
rs773152115 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83693025 | GATACATGATAGAAC[A/G]GGCCTCAAAGTATCC | 29979 |
rs773170305 | snp | A/G | | | upstream-variant-2KB, intron-variant | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83709725 | AAGATTTACCTGTAA[A/G]AAGATACCATATAGT | 29979 |
rs773189944 | snp | C/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83699561 | GCAGTGAGCCATGAT[C/G]ACTGAGCCATGGTGC | 29979 |
rs773292543 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83689298 | ATGAATATACCACCT[A/G]TTTTGCTTATCCACT | 29979 |
rs773411559 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83662600 | GGCCTACCTGATAAT[C/T]TGGAGGCTTGTAAGT | 29979 |
rs773441975 | snp | C/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83677472 | GAGGCTGAGGCAGAA[C/G]AATCACTTGAACCCA | 29979 |
rs773446123 | snp | A/G | 1.82891e-05 | 0.00302394 | missense | UBQLN1 | GRCh38.p7 | 9:83686118 | AACACAAGTTGGTCA[A/G]TATGTGATTTAAAAC | 29979 |
rs773455926 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83695991 | TGTTGCCAGGATAGA[A/G]TGCAGTCGCACGATC | 29979 |
rs773490182 | snp | C/T | 2.32307e-05 | 0.00340805 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83677677 | AAACAATGTTTTAAT[C/T]ATGTAAATGAGGACA | 29979 |
rs773571820 | in-del | -/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83687838 | CATTGCTAACATTTT[-/G]AAAAATAACCAAAAA | 29979 |
rs773578078 | snp | C/T | 1.65515e-05 | 0.00287671 | synonymous-codon | UBQLN1 | GRCh38.p7 | 9:83669257 | GGCAGACAACATGTT[C/T]TGCATCAGTTGTGGG | 29979 |
rs773622198 | snp | C/T | 1.64727e-05 | 0.00286986 | missense | UBQLN1 | GRCh38.p7 | 9:83679956 | TTAGACAAAAGTTGT[C/T]GCTGCATCTGACTCT | 29979 |
rs773702528 | snp | A/G | | | synonymous-codon, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83707608 | AGCGGCCGCGGGGGC[A/G]CCAGCACCTTCGGCT | 29979 |
rs773722012 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83696968 | AAAAAAAGATACAGA[A/G]TATTGCTATGTTGCC | 29979 |
rs773851286 | snp | G/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83695520 | TTATACTTTTCAACA[G/T]CATTTGAATTTCTTA | 29979 |
rs773861439 | snp | G/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83683730 | GACTATATAAAAAAC[G/T]TTTTTATCTTGGCCA | 29979 |
rs773949239 | snp | C/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83684975 | TTACAATTGCTGACA[C/G]CCAGGCATCAACTAC | 29979 |
rs773969165 | snp | A/G | 1.65754e-05 | 0.00287879 | missense | UBQLN1 | GRCh38.p7 | 9:83677940 | TATTGCTCACCAAGG[A/G]AGCAAATGGATTACC | 29979 |
rs774097549 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83664837 | GGTGAGAGAATCCCT[C/T]GAGCCCGAGAGGTCG | 29979 |
rs774100599 | snp | A/G | 0.000151711 | 0.00870817 | synonymous-codon, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83707641 | GGCGGCGCTATCCTG[A/G]GAGCCCGGAGGACCG | 29979 |
rs774124189 | snp | C/G | 1.67632e-05 | 0.00289505 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83678416 | AAGCTACTCCTTGGC[C/G]TGAACCTTGGAGCCA | 29979 |
rs774179423 | snp | A/T | | | utr-variant-3-prime | UBQLN1 | GRCh38.p7 | 9:83661184 | GTAAGATTCTATACA[A/T]TTAGGAAATACTCAG | 29979 |
rs774256272 | in-del | -/T | 1.67536e-05 | 0.00289423 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83682922 | GAGTATTTTTTCCCA[-/T]CCCTACTGGAATGAC | 29979 |
rs774256908 | in-del | -/TTTTTTGTACCCTTTTTTTTTTTTTTTTTTTT | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83697722 | CACCACACGCGGCTA[lengthTooLong]GAGACGAAGTCTCAC | 29979 |
rs774289101 | snp | G/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83703686 | CTAGCAACCTGTAAG[G/T]AAAAATTTATGTTAC | 29979 |
rs774451365 | snp | A/C | 3.29658e-05 | 0.00405978 | missense | UBQLN1 | GRCh38.p7 | 9:83677804 | CTACCAGTAGTGCCA[A/C]CCACAGTGCTGGCAG | 29979 |
rs774477788 | snp | A/T | | | downstream-variant-500B | UBQLN1 | GRCh38.p7 | 9:83659571 | AACCCCTTAAGATGT[A/T]GATATTTATCTTTAG | 29979 |
rs774556022 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83671288 | CATCCTCTCCATGAA[C/T]TAGGAACGTTCTTAA | 29979 |
rs774607608 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83706329 | TCCCAATTCTTTCAA[C/T]TTTCCGCATGCTTGA | 29979 |
rs774798693 | snp | C/T | 4.94295e-05 | 0.00497115 | missense | UBQLN1 | GRCh38.p7 | 9:83679990 | GTTCAGAGAAGTTGG[C/T]AGTATTCAAACCCAA | 29979 |
rs774851914 | snp | A/G | 4.97888e-05 | 0.00498918 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83682939 | CCTACTGGAATGACT[A/G]AAGACACTTACCTAA | 29979 |
rs774851976 | snp | A/T | 3.29625e-05 | 0.00405958 | missense | UBQLN1 | GRCh38.p7 | 9:83665084 | AAACCCTGCTGAATC[A/T]GTAACAAGGCCTGCA | 29979 |
rs774854241 | snp | G/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83678378 | AGCTACCCTCAATCA[G/T]ACACATATTTGTGTT | 29979 |
rs774910595 | snp | A/C | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83677330 | CAATTTGGGAGGCCA[A/C]GGCAGGCGGATCACC | 29979 |
rs774931256 | snp | C/T | | | intron-variant, downstream-variant-500B | UBQLN1 | GRCh38.p7 | 9:83667438 | CTGGTAGAGAAAATT[C/T]GCCCCAATTCTTGCA | 29979 |
rs774957314 | snp | A/C | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83682807 | CTTCCTTAATATCTA[A/C]AATTATAGGAATGTA | 29979 |
rs774974937 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83707246 | GGCTGAGGGTCGGCG[A/G]ATACCAGAGAAGGAA | 29979 |
rs774984461 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83694595 | AAATGTTAGTGTATC[A/G]TTCAGAAAATTTATT | 29979 |
rs775014651 | snp | A/G | | | intron-variant, utr-variant-3-prime | UBQLN1 | GRCh38.p7 | 9:83667555 | ACCAGTAAGTTCACA[A/G]TAAGTAAACTCATAC | 29979 |
rs775044665 | snp | A/G | 1.64895e-05 | 0.00287132 | synonymous-codon, intron-variant | UBQLN1 | GRCh38.p7 | 9:83666415 | GATTTCCAGCAAATA[A/G]GGGATTATTCAGCAT | 29979 |
rs775190340 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83704040 | AGAAATTTTAACTTA[C/T]AGAAAACGGAATTTG | 29979 |
rs775198888 | snp | A/G | 1.72089e-05 | 0.00293328 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83678626 | ATTTCCAAAAAAAGA[A/G]AAAAAAAAGGCATTG | 29979 |
rs775202824 | in-del | -/A/AA | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83690745 | ACCAGACTCTGTCTC[-/A/AA]AAAAAAAAAAACAAG | 29979 |
rs775206388 | snp | A/G | 1.65501e-05 | 0.00287659 | synonymous-codon | UBQLN1 | GRCh38.p7 | 9:83669265 | ACATGTTTTGCATCA[A/G]TTGTGGGTTTTCAGT | 29979 |
rs775226879 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83673678 | AATTCAAATTTCAAC[A/G]CCCATGAATACCATT | 29979 |
rs775294883 | snp | C/T | 1.87475e-05 | 0.0030616 | synonymous-codon | UBQLN1 | GRCh38.p7 | 9:83686123 | AAGTTGGTCAGTATG[C/T]GATTTAAAACGTTTA | 29979 |
rs775311068 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83681269 | ACAAAGTGTTTACTT[C/T]GTAAAATTACATAAC | 29979 |
rs775312452 | snp | C/T | 5.31463e-05 | 0.00515464 | intron-variant, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83707484 | CCATCCCGGCCCGAG[C/T]CCCAGGCGGCCTCAC | 29979 |
rs775313033 | in-del | -/CA | 1.71898e-05 | 0.00293166 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83669153 | TTTTAATTCACACTG[-/CA]CAGTCTTTTTCAATA | 29979 |
rs775337614 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83702189 | TGCTAAAGGGTACAG[C/T]GTTTCTTTTTGAGGG | 29979 |
rs775386134 | snp | A/C | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83701388 | CTCTAGCCAAGTGCA[A/C]TGCCCAGTTTTGAGA | 29979 |
rs775405000 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83680644 | GCCCAACTTCCATCC[C/T]CCACATACCCATACC | 29979 |
rs775417047 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83672871 | AAGATAGGCTGGCAA[A/G]TAACAGCCTGCAGGA | 29979 |
rs775439496 | in-del | -/G | 1.76204e-05 | 0.00296814 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83680070 | AAAACATACAAATCA[-/G]AAGTCAGAAAATTTA | 29979 |
rs775501886 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83662738 | TATCAGGAATACAGA[C/T]ATGTATGAGACAGAA | 29979 |
rs775538559 | snp | A/G | 1.67323e-05 | 0.00289239 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83664075 | TAGGAAATATCCTAA[A/G]GTCCTGCAAAACCAG | 29979 |
rs775601249 | snp | A/G | 3.37336e-05 | 0.00410678 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83663825 | TTTTTGGAAATTTCT[A/G]AATTTCCAACATTAA | 29979 |
rs775606709 | snp | A/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83669686 | TTCCTCCAAGACTGC[A/T]AAGAATTAATTAGAA | 29979 |
rs775694796 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83681577 | CGTGAAGAAGGTTAG[A/G]AGGGGGACTGAATAC | 29979 |
rs775709776 | snp | A/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83699644 | ACCACTGAGCCCAGC[A/T]CACATTGTATTTCTA | 29979 |
rs775710656 | snp | A/C | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83674550 | CAAGTACTAGTGATG[A/C]CTAATTTAACAGTTA | 29979 |
rs775754112 | snp | A/G | 1.6951e-05 | 0.00291122 | utr-variant-3-prime | UBQLN1 | GRCh38.p7 | 9:83661740 | TTTTAAAGTTTAAGA[A/G]CCGTTATCAAAAATA | 29979 |
rs775870488 | snp | A/G | | | utr-variant-3-prime | UBQLN1 | GRCh38.p7 | 9:83660239 | CCTCTTAACCTTTTT[A/G]ATAGCAAGCAACATA | 29979 |
rs775973719 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83687645 | GACAAGGAAGGGAAG[A/G]CATATATAAAAAACA | 29979 |
rs775996344 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83686640 | AGTTAGCTCTTACCA[C/T]GTCCAAAATAATCCA | 29979 |
rs776014807 | snp | G/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83687918 | TCCATCTGCATTCTT[G/T]CCTTTATTTGAAATC | 29979 |
rs776028027 | snp | A/G | 1.64868e-05 | 0.00287109 | missense | UBQLN1 | GRCh38.p7 | 9:83683049 | GTATTTGTTTGCTGA[A/G]CTGAATGATCCTGAG | 29979 |
rs776041084 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83686475 | ATCTTGATGTTAGTA[A/G]GAAATGATTATTACT | 29979 |
rs776081346 | snp | C/T | 1.65321e-05 | 0.00287502 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83666463 | TTCAAACAATTTTAA[C/T]TGGAAATATCTGAAA | 29979 |
rs776098144 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83693456 | TTGTATCTGCCTTTT[C/T]CTTTTTCTTATTTTT | 29979 |
rs776110663 | snp | A/C | 1.66546e-05 | 0.00288566 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83678633 | AAAAAAGAAAAAAAA[A/C]AGGCATTGAAATACA | 29979 |
rs776117625 | in-del | -/T | 8.69709e-05 | 0.00659378 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83665002 | GTAACCATTATACAC[-/T]TTCATTATCTTCCCC | 29979 |
rs776135233 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83689168 | ATAAATGCAATATTA[C/T]AACATATGGTCTTTG | 29979 |
rs776177363 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83674927 | CATGGCAGCAAAAAC[A/G]TGCAGAATTAAAACG | 29979 |
rs776185980 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83665297 | CCAAAATAAACGCAA[A/G]TATCTCCTCTTTGAC | 29979 |
rs776196866 | in-del | -/AAACCAA | 1.67514e-05 | 0.00289403 | splice-acceptor-variant | UBQLN1 | GRCh38.p7 | 9:83680039 | CCCCCAAGGCCACCT[-/AAACCAA]AAGAGGATAAAGGGC | 29979 |
rs776349691 | snp | A/C/T | 3.29806e-05 | 0.00406071 | missense | UBQLN1 | GRCh38.p7 | 9:83665055 | GGCCCGGGGCTTCCG[A/C/T]TGCTAATGTCTGTAA | 29979 |
rs776393015 | snp | A/C | | | intron-variant, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83705869 | AAAAATACACACAGT[A/C]CTATAGGCTCTATGG | 29979 |
rs776439465 | snp | A/G | 0.000101511 | 0.00712356 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83664090 | GGTCCTGCAAAACCA[A/G]AAGCCAGTCCGTAAA | 29979 |
rs776479765 | in-del | -/AAAAC | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83677566 | AAGCTCTATCTCAAA[-/AAAAC]AAAACAAAACAAAAC | 29979 |
rs776481284 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83694429 | CTGTCAGTTATCATT[C/T]TCCAAGAGTCTGATG | 29979 |
rs776500862 | snp | C/T | 2.24273e-05 | 0.0033486 | intron-variant, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83707497 | AGCCCCAGGCGGCCT[C/T]ACCTGCTGGACGGAG | 29979 |
rs776533779 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83681893 | CAGCAGAATGAAAAA[C/T]GACTTTCATTAGCTT | 29979 |
rs776552362 | snp | A/C/G | 7.3728e-05 | 0.00607121 | missense, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83707606 | GCAGCGGCCGCGGGG[A/C/G]CGCCAGCACCTTCGG | 29979 |
rs776554709 | snp | C/T | 1.65765e-05 | 0.00287888 | missense | UBQLN1 | GRCh38.p7 | 9:83677747 | ACTCCAGGCACCAAA[C/T]TTGGCGCAGTAGTAC | 29979 |
rs776582366 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83682649 | ATTATTATTCAGGGA[C/T]GCTGGCTTACGATTA | 29979 |
rs776648368 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83693163 | CATAAGAATCAAAAT[C/T]CTAATGCACCTTGAA | 29979 |
rs776708837 | in-del | -/TGTTT | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83678707 | TTTATGGGAGGCCAC[-/TGTTT]TGTTTTGTTTTTTTA | 29979 |
rs776725275 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83676974 | TAAATTTCTAACCTG[C/T]TCACACATGAGAATC | 29979 |
rs776797684 | snp | C/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83680450 | GCTGGTCACCAGAAA[C/G]ACAAAGTGATTAAAG | 29979 |
rs776823283 | in-del | -/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83686365 | CACTGCACTCCAGCC[-/T]TGGGTGACAGAGTGA | 29979 |
rs776913485 | snp | A/T | 1.65644e-05 | 0.00287783 | missense | UBQLN1 | GRCh38.p7 | 9:83686020 | TGTTTTGTGTTTTAA[A/T]GACAAGGTGAACAGT | 29979 |
rs776959523 | snp | C/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83669530 | CAGGAAAAGAGGACT[C/G]ATGAGTTTAAACATT | 29979 |
rs776994982 | snp | G/T | | | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83708020 | GGTAACGCGCCTGGC[G/T]GCGTCGCCGAGTCAT | 29979 |
rs777001547 | snp | C/T | 1.65971e-05 | 0.00288067 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83683081 | CCTAGGGAAAATAAT[C/T]AATCACAGAGTAAGC | 29979 |
rs777044436 | snp | C/G | | | upstream-variant-2KB, intron-variant | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83708515 | CGTATTGCCCTATGC[C/G]GGGGAGTTGGGGTAA | 29979 |
rs777104500 | snp | A/G | 1.648e-05 | 0.0028705 | synonymous-codon | UBQLN1 | GRCh38.p7 | 9:83678483 | TTCCTGAATATCTGT[A/G]TACATGCGCCTTAAA | 29979 |
rs777120280 | snp | C/T | | | upstream-variant-2KB, intron-variant | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83709348 | CAATCATTTGGAATT[C/T]CTTCCATATGTCTAA | 29979 |
rs777147326 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83686590 | AATATCCTTATTCTT[C/T]TTATGTTAATGAGAC | 29979 |
rs777187058 | in-del | -/TC | | | upstream-variant-2KB, intron-variant | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83709620 | GTGTGTGTGTGTGTG[-/TC]TCTGTCTCCCTGCAT | 29979 |
rs777196113 | snp | C/G | | | intron-variant, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83706635 | ACGTATTCAACAATA[C/G]ACTAAAATTATTTGT | 29979 |
rs777372353 | snp | C/G/T | 3.34388e-05 | 0.00408883 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83682925 | TATTTTTTCCCATCC[C/G/T]TACTGGAATGACTAA | 29979 |
rs777383666 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83670957 | AGTGTTCATGCTCCA[C/T]CTCTTTTTTTCTTTT | 29979 |
rs777424246 | snp | C/T | 1.64792e-05 | 0.00287042 | synonymous-codon | UBQLN1 | GRCh38.p7 | 9:83683012 | ATTAGGAGTTGATGA[C/T]GTAGTAACATTGCTT | 29979 |
rs777442630 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83687405 | TTCAGAGTGGGCCCA[A/G]GAATCTACATTAAAA | 29979 |
rs777443911 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83705680 | TTGTATAAGACTGTT[C/T]ATAGTAACTAACTGC | 29979 |
rs777462205 | in-del | -/GT | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83683273 | AAAAATTAGCCGGGC[-/GT]GATGGCGAGTGCCTA | 29979 |
rs777561089 | snp | C/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83697446 | AATCCCAGCTACTCA[C/G]GAGGCTGAGGCAAGA | 29979 |
rs777613349 | snp | A/C | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83676769 | TTTTAAAACATGCCC[A/C]GTCTATCTCATCTTA | 29979 |
rs777726954 | snp | C/G | | | intron-variant, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83706621 | TTATGGAAAACACGA[C/G]GTATTCAACAATACA | 29979 |
rs777751463 | snp | C/T | 1.67377e-05 | 0.00289284 | missense | UBQLN1 | GRCh38.p7 | 9:83669186 | AATTACAAACTCACC[C/T]GTGCAGCAAGGTCAG | 29979 |
rs777785259 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83686251 | GGCCCCTACTACAGA[C/T]GCTACAATTCAAACA | 29979 |
rs777801642 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83663664 | GTCTTCTCTACAACC[A/G]TAACAACGTTTCCTT | 29979 |
rs777838391 | snp | G/T | 3.30715e-05 | 0.00406628 | synonymous-codon | UBQLN1 | GRCh38.p7 | 9:83665032 | CAAATAAGCCTACCC[G/T]GGGATGAGGCCCGGG | 29979 |
rs777873273 | snp | G/T | 3.59202e-05 | 0.00423778 | intron-variant, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83707462 | GGCGGAGGTCCTGCC[G/T]CCACCCCCATCCCGG | 29979 |
rs778044931 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83680888 | GTCTTGCAGGACTGA[A/G]TCTGCTAACTTGTGA | 29979 |
rs778074951 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83681348 | CAGAGACTGTGTTAC[A/G]TATGTATTGAGAATA | 29979 |
rs778080494 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83691547 | GGCTTCTCTACAATG[C/T]CCTAGATGCAGTAGA | 29979 |
rs778087633 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83664730 | ACATGGCAAAGCTCC[A/G]TCTCTAAAAACAGTA | 29979 |
rs778102600 | in-del | -/A/AA | 0.0279109 | 0.115372 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83678624 | TATTTCCAAAAAAAG[-/A/AA]AAAAAAAAAAGGCAT | 29979 |
rs778103265 | in-del | -/AT | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83691200 | ACACATATAATACAT[-/AT]ATATATATATATGCC | 29979 |
rs778168821 | snp | A/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83670197 | ATACACTCAAACTCA[A/T]ATATATTCTCAAACT | 29979 |
rs778169665 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83682650 | TTATTATTCAGGGAC[A/G]CTGGCTTACGATTAA | 29979 |
rs778218868 | snp | C/T | 0.000217681 | 0.0104304 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83661963 | GAAAAAAAAAATTAA[C/T]CCAACTCTAAAGGAA | 29979 |
rs778261003 | snp | A/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83679716 | TCATTAACCACAGAA[A/T]ATTAAATAACAAATA | 29979 |
rs778273364 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83698322 | TATTAGCTGTGCTAA[C/T]TCAGCAGTCACTAGC | 29979 |
rs778295044 | in-del | -/CAGGCAAGCAGGAGGGAG | 0.000169334 | 0.0091999 | utr-variant-5-prime, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83707707 | GCGGCGGCGGTGACT[-/CAGGCAAGCAGGAGGGAG]CAGGCAAGCAGGAGG | 29979 |
rs778378034 | snp | C/T | | | upstream-variant-2KB, intron-variant | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83709140 | GACTTTTTAGCAGAG[C/T]TCTATGGAATCTGGG | 29979 |
rs778447675 | snp | A/G | 0.000230684 | 0.0107373 | missense | UBQLN1 | GRCh38.p7 | 9:83677891 | GGATCTCTATTTTCT[A/G]TACGGGAAGGTTGAC | 29979 |
rs778499407 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83698492 | AATATTTTAGACATA[C/T]TGGGTTAAATAAAGC | 29979 |
rs778502417 | snp | C/T | | | upstream-variant-2KB, intron-variant | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83709042 | ACAGCCCACTATGAC[C/T]CAAATCCGCAAAGAT | 29979 |
rs778524765 | snp | C/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83681180 | GCCAGGGAATACCTG[C/G]AAATAGATTTCTCTT | 29979 |
rs778537204 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83696218 | ACTTATAAAGTACAA[C/T]ATGATGTCTTGATAT | 29979 |
rs778654499 | snp | A/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83686455 | TGCATCCTTTTTATG[A/T]CAGTATCTTGATGTT | 29979 |
rs778718271 | snp | A/C | | | | | GRCh38.p7 | 9:83707442 | AAAGGTCTCCTGGGG[A/C]GGCGGGCGGAGGTCC | 29979 |
rs778746441 | snp | C/T | | | | | GRCh38.p7 | 9:83687267 | TCCAGGGACCAGACA[C/T]ATAAAACCAGACAAG | 29979 |
rs778835811 | snp | C/T | 3.34152e-05 | 0.00408736 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83664069 | CACAAATAGGAAATA[C/T]CCTAAGGTCCTGCAA | 29979 |
rs778919850 | snp | A/C/T | 0.000117604 | 0.00766748 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83679750 | CATTTTTTAGCTAAA[A/C/T]GAACTGAAAGAACTT | 29979 |
rs779029569 | in-del | -/TGTC | | | upstream-variant-2KB, intron-variant | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83709619 | GTGTGTGTGTGTGTG[-/TGTC]TGTCTCCCTGCATTT | 29979 |
rs779067338 | snp | A/C/T | 0.000134877 | 0.00821115 | synonymous-codon, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83707599 | CGCGGAGGCAGCGGC[A/C/T]GCGGGGGCGCCAGCA | 29979 |
rs779118802 | snp | A/G | 2.05139e-05 | 0.00320258 | utr-variant-5-prime, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83707687 | TCGGCCATGGCTGTG[A/G]CGGCGGCGGCGGCGG | 29979 |
rs779134779 | snp | C/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83680751 | GTGTTTCCTTGAGTT[C/G]TAGGTGCCATTCTAG | 29979 |
rs779200111 | snp | A/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83683159 | GGCTCACGCCTGTAA[A/T]CCCAGCACTTTGGGA | 29979 |
rs779210340 | snp | C/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83684454 | CCCACCTCACCCTCC[C/G]AAAGTGCTCAGATTT | 29979 |
rs779268720 | snp | A/G | 1.84089e-05 | 0.00303383 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83677993 | AAAAAATCACAAAGA[A/G]TAAGCTTTTGTTTTA | 29979 |
rs779296209 | snp | A/C | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83703732 | TGCTCCGTGAATAAT[A/C]AATTTCACTCTAAAT | 29979 |
rs779307878 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83679258 | CATCTGCTTTTTGTT[C/T]GTTTTTGCTTTCTTC | 29979 |
rs779322288 | snp | A/G | 1.64942e-05 | 0.00287173 | synonymous-codon | UBQLN1 | GRCh38.p7 | 9:83663896 | ATTTACTCCAGCAAG[A/G]GCCTGCAGCATCTGC | 29979 |
rs779334577 | in-del | -/A | 0.00699132 | 0.0587093 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83661948 | CTGTAGCTATTAAAG[-/A]AAAAAAAAAATTAAT | 29979 |
rs779432274 | in-del | -/T | 1.64749e-05 | 0.00287005 | frameshift-variant | UBQLN1 | GRCh38.p7 | 9:83678507 | CCTTAAAGCATTATA[-/T]CCCCCTGGGATGCTT | 29979 |
rs779453104 | snp | A/G | 1.69097e-05 | 0.00290768 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83661976 | AATCCAACTCTAAAG[A/G]AAGCCAGTCCCTGCC | 29979 |
rs779506759 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83670921 | GTACAAGTTTTTTCA[C/T]GGCATTGTAGCAACG | 29979 |
rs779604497 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83669168 | CACAGTCTTTTTCAA[C/T]ACAATTACAAACTCA | 29979 |
rs779629906 | snp | C/T | | | upstream-variant-2KB, nc-transcript-variant | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83708274 | AAAGGGACCAGTGGG[C/T]CCTGCGGCCGCGGCT | 29979 |
rs779685859 | snp | A/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83689755 | CAGAGTAAAAAGATA[A/T]GCCCTTAAAGAGACA | 29979 |
rs779737724 | snp | C/T | 5.33879e-05 | 0.00516634 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83669337 | TACTAGCTGAAAGTT[C/T]GTTTTTAAAAAAGAC | 29979 |
rs779789865 | snp | A/G | | | upstream-variant-2KB, intron-variant | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83708985 | TGCAAGGAATGTACA[A/G]ACCAGCCCATTATTA | 29979 |
rs779931062 | snp | A/G | 3.34012e-05 | 0.0040865 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83665177 | ACTAGTGGTTACAAA[A/G]GAATTAAAATCAGTG | 29979 |
rs779974686 | snp | A/G | | | missense | UBQLN1 | GRCh38.p7 | 9:83683016 | GGAGTTGATGATGTA[A/G]TAACATTGCTTCCAG | 29979 |
rs780044373 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83666907 | GAAAAGGACCACTAC[A/G]TCTACCTGCCTACTA | 29979 |
rs780060525 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83674450 | TGAAATATCTCATCA[C/T]AGCCACTTTTTCACA | 29979 |
rs780064526 | in-del | -/GCCTCA | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83705355 | AGCGATGATTCTCCT[-/GCCTCA]GCCTCAGCCTCAGCC | 29979 |
rs780111437 | snp | C/T | 1.6489e-05 | 0.00287128 | missense | UBQLN1 | GRCh38.p7 | 9:83679797 | ATTATATCTGGATTA[C/T]TCAACATATGACTAA | 29979 |
rs780112530 | snp | A/T | 1.64749e-05 | 0.00287005 | synonymous-codon | UBQLN1 | GRCh38.p7 | 9:83663950 | TTCAGTGGTTCCTGC[A/T]GTGGGACTTGTGTTT | 29979 |
rs780166648 | snp | A/G | 1.64966e-05 | 0.00287194 | synonymous-codon | UBQLN1 | GRCh38.p7 | 9:83665047 | TGGGATGAGGCCCGG[A/G]GCTTCCGTTGCTAAT | 29979 |
rs780166687 | snp | A/T | 1.84269e-05 | 0.00303531 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83680088 | GTCAGAAAATTTATC[A/T]TTAACATGACATAAA | 29979 |
rs780185554 | in-del | -/TA | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83662245 | ATGCAGAAAAACCTG[-/TA]TGTGTGTGTGTATAT | 29979 |
rs780272768 | snp | A/G | 1.68519e-05 | 0.0029027 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83678391 | CATACACATATTTGT[A/G]TTAAAACAGAAGCTA | 29979 |
rs780276567 | snp | G/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83671172 | TGCTATTTCCACTAC[G/T]TCTACAGTCCCCTCC | 29979 |
rs780343778 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83683082 | CTAGGGAAAATAATT[A/G]ATCACAGAGTAAGCA | 29979 |
rs780351448 | snp | A/T | 1.65784e-05 | 0.00287905 | missense | UBQLN1 | GRCh38.p7 | 9:83669230 | TGACTGCATCATGCT[A/T]CTCATGTAGGGGGCA | 29979 |
rs780389959 | snp | A/C | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83701922 | ACCCAATGTCCACCA[A/C]GTGATAGAAAAATAA | 29979 |
rs780432842 | in-del | -/AGAA | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83704824 | CAGAGACTCCATCTC[-/AGAA]AAAAAAAAAAAAAAA | 29979 |
rs780436208 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83672266 | ATGTCTTCACTGGAG[C/T]AGCACTTATAATTTT | 29979 |
rs780446188 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83678272 | GGGATCCACCCGCCT[C/T]GGCCTCCCAAAGTGC | 29979 |
rs780523687 | snp | C/G | 1.65302e-05 | 0.00287486 | missense | UBQLN1 | GRCh38.p7 | 9:83664036 | ATGCCCCCAAGCCAG[C/G]AGTAAACCTACAGAA | 29979 |
rs780540052 | snp | A/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83663364 | TGCAACCACATTATT[A/T]GGGGGTCCATATTCT | 29979 |
rs780541465 | in-del | -/A | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83682721 | AGATCAGGTATACAC[-/A]AACTACATCTCTTTC | 29979 |
rs780630998 | snp | C/T | 1.681e-05 | 0.00289909 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83682916 | GGAAAGGAGTATTTT[C/T]TCCCATCCCTACTGG | 29979 |
rs780797431 | snp | A/G | | | upstream-variant-2KB, intron-variant | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83709988 | TTGTATCACAGAGTA[A/G]TCATAGACAATACAT | 29979 |
rs780814783 | snp | C/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83700460 | GAGCCCTAGGCTCTG[C/G]TAACACAATGGTGAA | 29979 |
rs780834056 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83676860 | TGTCACTATGGCTAA[C/T]GATCTTGGACCTAAT | 29979 |
rs780887825 | in-del | -/TT | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83697735 | TATTTTTTGTACCCT[-/TT]TTTTTTTTTTTTTTT | 29979 |
rs780890784 | snp | C/T | | | intron-variant, utr-variant-3-prime | UBQLN1 | GRCh38.p7 | 9:83667937 | AGTAAAAAAATAGTA[C/T]GTGAGTGCTCAAGTC | 29979 |
rs780915688 | snp | A/C/G | 3.29458e-05 | 0.00405857 | synonymous-codon | UBQLN1 | GRCh38.p7 | 9:83679925 | ATTTTCCATGATCTG[A/C/G]ACCATCATTTCAGGG | 29979 |
rs780932968 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83670774 | CAAACCCTGCCACTG[C/T]TTTATCAACAAAGTT | 29979 |
rs781022586 | snp | C/G | | | intron-variant, utr-variant-3-prime | UBQLN1 | GRCh38.p7 | 9:83668248 | TTACTGAGAATTATA[C/G]ACAAAGATACCTGAA | 29979 |
rs781142593 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83696250 | TGTAAACAATGTGGA[A/G]TGACTAAATCAAGCT | 29979 |
rs781165461 | snp | C/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83675419 | TTGACAACTAAAATT[C/G]TTTGAATCACAAGCA | 29979 |
rs781185914 | snp | A/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83685007 | TGCCTGCACATGTAG[A/T]CTACATGACTTCAAC | 29979 |
rs781216899 | snp | A/T | 1.6486e-05 | 0.00287102 | missense, intron-variant | UBQLN1 | GRCh38.p7 | 9:83666403 | CTTGAAGCTGAGGAT[A/T]TCCAGCAAATAGGGG | 29979 |
rs781234678 | snp | A/C | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83692659 | GCAGTTTGAGACCAG[A/C]CTGACCAACATGGAG | 29979 |
rs781245730 | in-del | -/C | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83683810 | GCGATCAACTGAGGT[-/C]CAGGAGTTCAAGACC | 29979 |
rs781453980 | in-del | -/AAAAACA | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83666119 | TAGGTCCTCAAAAGC[-/AAAAACA]AAAAACAAAATGTTC | 29979 |
rs781460635 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83664745 | ATCTCTAAAAACAGT[A/G]ACAACAACAAATTAT | 29979 |
rs781584199 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83698767 | AAAAAATACAAAGTA[A/G]CCAAGCATGGTGATG | 29979 |
rs781594048 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83693842 | CTACATACTAGTTGT[A/G]TGACCTGGAGGATGT | 29979 |
rs781606776 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83682199 | CTGAGGCAGAAGAAT[C/T]GCTTGAACCCAGGAG | 29979 |
rs781622319 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83671099 | ACCTTCCAAAGTGCC[A/G]TGATTAAAGGTATGA | 29979 |
rs781745568 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83699362 | TTTTTGTTTTTAAGA[A/G]ACCAAGTCTCATTCT | 29979 |
rs781757120 | snp | C/G | 3.92088e-05 | 0.00442751 | intron-variant, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83707454 | GGGCGGCGGGCGGAG[C/G]TCCTGCCGCCACCCC | 29979 |
rs781769627 | snp | A/G | 5.9574e-05 | 0.00545742 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83669365 | GACATATTAAGGAAA[A/G]ATACTTAAACAAAAG | 29979 |
rs796296506 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83703685 | TCTAGCAACCTGTAA[A/G]TAAAAATTTATGTTA | 29979 |
rs796297148 | in-del | -/A | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83696658 | AGGAAAAAAAAAAAA[-/A]TCCCAACTAGGTACA | 29979 |
rs796341436 | snp | A/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83673546 | CGAGACTCGGTCTTT[A/T]AAAAAAAAAAAAAAA | 29979 |
rs796404939 | in-del | -/A | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83662058 | TACTGAGCTTTAAAA[-/A]CACTGCCCACCTCTT | 29979 |
rs796497687 | in-del | -/AC | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83703368 | GATGGTTCAATGTAT[-/AC]AGTTTGTTTCACTCG | 29979 |
rs796554278 | in-del | -/C | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83673580 | AACAAAAAAAAAAAA[-/C]CTGCGCTTACGTTTT | 29979 |
rs796762281 | in-del | -/A | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83703162 | GATGAACAATTAACC[-/A]AAAAAAAAAAAATCT | 29979 |
rs796820849 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83685322 | GAGTTTGATACTGTA[C/T]GAAAAAATATGGACA | 29979 |
rs796864777 | in-del | -/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83693476 | TTCTTATTTTTTTTT[-/T]AACCAGACTGTCAAG | 29979 |
rs796954152 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83686353 | GCTATTATCACACCA[C/T]TGCACTCCAGCCTGG | 29979 |
rs797013439 | snp | C/T | | | downstream-variant-500B | UBQLN1 | GRCh38.p7 | 9:83659466 | TCTTTATTCAATTTG[C/T]ACTAAATATTATCAC | 29979 |