SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs11659 | snp | C/T | 0.0228947 | 0.104514 | utr-variant-3-prime | UBQLN1 | GRCh38.p7 | 9:83661661 | CTCCACCTTAAAATG[C/T]ATCATATTGGGTTTG | 29979 |
rs12404 | snp | C/G | 0.0123036 | 0.0774623 | utr-variant-3-prime | UBQLN1 | GRCh38.p7 | 9:83661494 | TCCTGCATCTGTCCA[C/G]TTTATTTGCTTTTTA | 29979 |
rs868917 | snp | C/T | 0.473266 | 0.112482 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83701483 | ACCCTTAACAGGGTA[C/T]GGGGACTCCCCAAAC | 29979 |
rs944946 | snp | A/G | 0.355311 | 0.226737 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83685354 | tcttgcataacatac[A/G]aagACTTagttgtca | 29979 |
rs944947 | snp | A/G | 0.2776 | 0.248472 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83685149 | CAACATATTCCTTCT[A/G]TTTTGGTGCTATTCT | 29979 |
rs961807 | snp | A/G | 0.35894 | 0.225016 | upstream-variant-2KB, intron-variant | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83710135 | AAACAAAAACCATTC[A/G]GAAGAAAATGCCACA | 29979 |
rs1044175 | snp | G/T | 0.428769 | 0.174761 | synonymous-codon | UBQLN1 | GRCh38.p7 | 9:83669263 | TGAAAACCCACAACT[G/T]ATGCAAAACATGTTG | 29979 |
rs1044214 | snp | G/T | 0.40733 | 0.194287 | utr-variant-3-prime | UBQLN1 | GRCh38.p7 | 9:83660644 | AGCGGAATCTGTCCT[G/T]GATGGGGCCAGCTTA | 29979 |
rs1044256 | snp | C/G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | UBQLN1 | GRCh38.p7 | 9:83660194 | AGTCCTTGCACTGTT[C/G/T]TGACACTTTCCCCAG | 29979 |
rs1056073 | snp | C/G | 0.473909 | 0.111197 | utr-variant-5-prime, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83707825 | CCCCACACCCGCTAC[C/G]GTGGCCCTGCGCCCG | 29979 |
rs1333861 | snp | A/G | 0.473266 | 0.112482 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83703483 | ATGAGATATCTTGGG[A/G]ATGGCACCTAAATAT | 29979 |
rs1333862 | snp | C/T | 0.473359 | 0.112298 | upstream-variant-2KB, intron-variant | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83709335 | AGAAATTCCAAATGA[C/T]TGGTTGTCCAGTTGT | 29979 |
rs1333863 | snp | C/G | 0.359575 | 0.224707 | upstream-variant-2KB, intron-variant | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83709067 | GCTTAGGAGCAGAAA[C/G]GCAGAATGTATCTTT | 29979 |
rs1333865 | snp | C/T | 0.359575 | 0.224707 | upstream-variant-2KB, intron-variant | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83708681 | ACTGTCAATACAGGT[C/T]GCCTGACTGATCGTC | 29979 |
rs1968216 | snp | C/T | 0.355311 | 0.226737 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83695488 | AAAGGGGACTGGGCA[C/T]GGCGCCTCACGCCTT | 29979 |
rs2042042 | snp | C/T | 0.352721 | 0.227922 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83683289 | AAGTAGCTGGGACTA[C/T]AGGCACTCGCCATCA | 29979 |
rs2058912 | snp | A/G | 0.355096 | 0.226837 | intron-variant, downstream-variant-500B | UBQLN1 | GRCh38.p7 | 9:83667080 | AAAAGATGTAAATCC[A/G]TTTGAGAACACCAAG | 29979 |
rs2542775 | snp | C/T | 0.354881 | 0.226936 | | | GRCh38.p7 | 9:83667733 | TCATCTTATTAGATA[C/T]TTCTTATAACTTACC | 29979 |
rs2542776 | snp | C/T | 0.355311 | 0.226737 | | | GRCh38.p7 | 9:83679618 | AATTCAGAGTTCAAA[C/T]AGCCAAATTAGCGCT | 29979 |
rs2542803 | snp | A/G | 0.355311 | 0.226737 | | | GRCh38.p7 | 9:83675821 | gtgttctgtttacca[A/G]aattgcaaagttcat | 29979 |
rs2542804 | snp | A/G | 0.176219 | 0.238865 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83673208 | tgagacagagtcgtc[A/G]cccaggctggagtgc | 29979 |
rs2780994 | snp | A/G | 0.17461 | 0.238362 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83678146 | tagtcccagctactc[A/G]ggaggctgaggcagg | 29979 |
rs2780995 | snp | A/C | 0.355311 | 0.226737 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83676253 | AAGGGAAAACAAGAA[A/C]TAGCAAGAATGAACT | 29979 |
rs2780996 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83672403 | gcatctcttacttta[A/T]atcaaaagctagaaa | 29979 |
rs2780997 | snp | C/T | 0.354665 | 0.227036 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83670832 | tgtaagtgaagatgc[C/T]gtgaacattattgaa | 29979 |
rs2780998 | snp | A/G | 0.354665 | 0.227036 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83670822 | gatgctgtgaacatt[A/G]ttgaaatgacaacga | 29979 |
rs2780999 | snp | A/T | 0.355096 | 0.226837 | intron-variant, utr-variant-3-prime | UBQLN1 | GRCh38.p7 | 9:83667859 | GATAATTTAGAAACT[A/T]TTACAATGTTCTTGT | 29979 |
rs2781000 | snp | C/T | 0.354881 | 0.226936 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83665932 | TAGAAGGCTTTTTTT[C/T]CCCAAGGGGTAGATC | 29979 |
rs2781001 | snp | C/T | 0.352938 | 0.227824 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83665541 | GTAAAATTGTTATAT[C/T]AGTAACAGATAACAC | 29979 |
rs2781002 | snp | A/G | 0.406641 | 0.194842 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83664110 | TTATATTAAAATGTA[A/G]CTGATTTACGGACTG | 29979 |
rs2781003 | snp | A/G | 0.355311 | 0.226737 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83664100 | ATGTAACTGATTTAC[A/G]GACTGGCTTCTGGTT | 29979 |
rs2781004 | snp | A/G | 0.237527 | 0.249689 | synonymous-codon | UBQLN1 | GRCh38.p7 | 9:83663998 | CACTGGAGGCTCTTC[A/G]GGAACTAATGGATCT | 29979 |
rs2811928 | snp | G/T | 0.356811 | 0.226034 | downstream-variant-500B | UBQLN1 | GRCh38.p7 | 9:83659928 | TTAGCAAAAGTTAAA[G/T]ACTTTTTTTCTTTCT | 29979 |
rs2811929 | snp | A/G | 0.35574 | 0.226537 | intron-variant, utr-variant-3-prime | UBQLN1 | GRCh38.p7 | 9:83668508 | GGAGAAAGGGTTATC[A/G]GACGCAATTATCTCA | 29979 |
rs2811930 | snp | C/T | 0.354881 | 0.226936 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83668935 | TCCTAACTCAACATA[C/T]GTAGAAACAAACTAA | 29979 |
rs2811931 | snp | A/C | 0.354881 | 0.226936 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83671106 | aaagtgccgtgatta[A/C]aggtatgagccaaca | 29979 |
rs2811932 | snp | A/C | 0.364609 | 0.222182 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83673580 | AAACAAAAAAAAAAA[A/C]CTGCGCTTACGTTTT | 29979 |
rs3763626 | snp | C/G | 0.0275645 | 0.114116 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83686325 | TGAGTCCAGGAGTTC[C/G]AGGCTGCAGTGAGCT | 29979 |
rs3814505 | snp | A/G | 0.473266 | 0.112482 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83708242 | CGAGATGACGTCACG[A/G]TTAGCGAAATTACTA | 29979 |
rs3814506 | snp | C/T | 0.0368353 | 0.130617 | upstream-variant-2KB, intron-variant, nc-transcript-variant | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83708359 | GGGCCGTGTTCACCC[C/T]TCCGCGCTGTCACAA | 29979 |
rs3814507 | snp | C/T | 0.343701 | 0.231776 | upstream-variant-2KB, intron-variant, nc-transcript-variant | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83708394 | CTTGCCCTCCCTTGC[C/T]TCTCTGTCTACTCTG | 29979 |
rs3818759 | snp | A/C | 0.031825 | 0.122064 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83663564 | TTTTTAAAGCAAAAT[A/C]TATTTCAAATGATTT | 29979 |
rs4146741 | snp | C/T | 0.355311 | 0.226737 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83694208 | TCTGAAGATAAAACA[C/T]ACACAATTTCATTTC | 29979 |
rs4242623 | snp | A/C | 0.357877 | 0.225527 | intron-variant, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83706562 | GTTGTTTCCTGTCAC[A/C]AACTGTTCACGTTGT | 29979 |
rs4454364 | snp | C/T | 0.479583 | 0.0989539 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83705126 | TAAAATTACAGAGAC[C/T]GACAATATCAAAATG | 29979 |
rs4877263 | snp | A/G | 0.355311 | 0.226737 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83692709 | AATACAAAATTATCC[A/G]GGCATGGTGGCAAAT | 29979 |
rs4877791 | snp | A/G | 0.450483 | 0.149354 | intron-variant, downstream-variant-500B | UBQLN1 | GRCh38.p7 | 9:83667426 | GCAATGTAAATGCTG[A/G]TAGAGAAAATTCGCC | 29979 |
rs4877793 | snp | C/T | 0.473451 | 0.112115 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83674173 | tcatgcagcacaaaa[C/T]cactgcagcattaaa | 29979 |
rs4877794 | snp | C/T | 0.471388 | 0.116136 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83674328 | GTGTTTCTTATGCAA[C/T]GACACTAAAAGAATA | 29979 |
rs4877796 | snp | G/T | 0.479421 | 0.0993283 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83689093 | cccacctatggctca[G/T]cacttccaaccataa | 29979 |
rs4877797 | snp | A/G | 0.473266 | 0.112482 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83691298 | CTGGATATAAGACAT[A/G]AAAATGACAACAGAG | 29979 |
rs4877798 | snp | C/T | 0.355311 | 0.226737 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83693024 | AGATACATGATAGAA[C/T]GGGCCTCAAAGTATC | 29979 |
rs4877799 | snp | A/G | 0.473359 | 0.112298 | intron-variant, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83706402 | ACAAAAACAAAAGTG[A/G]TAATTCTGTTGGTGG | 29979 |
rs5898834 | in-del | -/A | 0.357877 | 0.225527 | intron-variant, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83706127 | TGCCAAAATTACGTC[-/A]AAAAAACGTAAAAAA | 29979 |
rs6559737 | snp | A/T | 0.355954 | 0.226437 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83689212 | atacttggcatgttt[A/T]caagattcacccatg | 29979 |
rs6559738 | snp | C/T | 0.0685596 | 0.171987 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83696002 | tagagtgcagtcgca[C/T]gatctcagctcactg | 29979 |
rs6559739 | snp | A/G | 0.355096 | 0.226837 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83696137 | tagagacagggtttc[A/G]ccatgttggccagga | 29979 |
rs6559740 | snp | A/G | 0.466515 | 0.124985 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83696269 | ctaaatcaagctaat[A/G]tatctatcacctctc | 29979 |
rs7026362 | snp | A/G | 0.0644693 | 0.167566 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83691348 | AGATGATCCATTAAC[A/G]TCGTATGTGGCAGAG | 29979 |
rs7030866 | snp | C/T | 0.427879 | 0.175668 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83662269 | GTGTATATACATATA[C/T]ATATACACACACACA | 29979 |
rs7033585 | snp | C/T | 0.155987 | 0.23165 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83675190 | ttgatggtggcttag[C/T]agaggtaaagtttca | 29979 |
rs7035771 | snp | C/G | 0.155987 | 0.23165 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83686503 | ACTTCATCTCTAACA[C/G]AAAGGTCCTACTATA | 29979 |
rs7045761 | snp | C/T | 0.2776 | 0.248472 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83674545 | gaagccaagtactag[C/T]gatgactaatttaac | 29979 |
rs7046251 | snp | A/C | 0.0644693 | 0.167566 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83670749 | ctttcaaaattggag[A/C]caatcctctcaaacc | 29979 |
rs7846925 | snp | C/T | 0.164546 | 0.234942 | intron-variant, utr-variant-3-prime | UBQLN1 | GRCh38.p7 | 9:83667734 | CATCTTATTAGATAC[C/T]TCTTATAACTTACCT | 29979 |
rs7848643 | snp | C/T | 0.0752113 | 0.178743 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83672203 | ctatccagatcacta[C/T]aattttctccacatc | 29979 |
rs7850944 | snp | C/T | 0.355311 | 0.226737 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83698669 | TGTATAATCCTAGCA[C/T]TTTGGGAGACCAAGG | 29979 |
rs7851316 | snp | A/G | 0.00953873 | 0.0683987 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83707959 | CGCTTCCTCCTCCCT[A/G]CCCCTTCCCCCACGT | 29979 |
rs7851817 | snp | A/C/G | 0.0810805 | 0.184299 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83678273 | ggatccacccgcctc[A/C/G]gcctcccaaagtgct | 29979 |
rs7853146 | snp | A/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83673603 | TACgtttttattttt[A/T]aatagttaagggaaa | 29979 |
rs7856081 | snp | C/G | 0.467132 | 0.12391 | upstream-variant-2KB, intron-variant | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83709622 | TGTGTGTGTGTGTGT[C/G]TGTCTCCCTGCATTT | 29979 |
rs7857256 | snp | C/T | 0.0644693 | 0.167566 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83704554 | ACTGggccgggtgcc[C/T]ggtggttcacacctg | 29979 |
rs7858992 | snp | A/G | 0.081446 | 0.184634 | upstream-variant-2KB, intron-variant | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83709724 | TAAGATTTACCTGTA[A/G]GAAGATACCATATAG | 29979 |
rs7860614 | snp | A/G | 0.479583 | 0.0989539 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83704775 | AGGTTGCAGTGAGCC[A/G]ACACCATGCCATTGC | 29979 |
rs7863266 | snp | C/T | 0.479744 | 0.0985793 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83677510 | GAGGTTGCGGTGAGC[C/T]GAGATCGTGCCATTG | 29979 |
rs7865296 | snp | A/C | 0.355311 | 0.226737 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83699280 | CACCACTATTGAAAA[A/C]TTGACTTCAGTCCTT | 29979 |
rs7866234 | snp | A/C | 0.435973 | 0.167075 | synonymous-codon | UBQLN1 | GRCh38.p7 | 9:83663902 | TCCAGCAAGAGCCTG[A/C]AGCATCTGCTGAATA | 29979 |
rs7866837 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83678087 | agtgcagtggcgcga[A/T]ctcggctcactgcaa | 29979 |
rs7868710 | snp | A/T | 0.0584853 | 0.160693 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83696467 | caaacaaaaaaattt[A/T]aaaaaaaaacccaat | 29979 |
rs7874980 | snp | C/T | 0.23031 | 0.249223 | upstream-variant-2KB, intron-variant | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83709989 | TGTATCACAGAGTAA[C/T]CATAGACAATACATA | 29979 |
rs7875986 | snp | A/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83704821 | gtgacagagactcca[A/T]ctcaaaaaaaaaaaa | 29979 |
rs9314722 | snp | C/T | 0.30472 | 0.243938 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83663858 | AATACAAAACTTGAA[C/T]GGAAAAGAACTGATA | 29979 |
rs9987871 | snp | A/G | 0.277867 | 0.248442 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83663114 | ggaaagaggaaaaag[A/G]ggaaagggggaaggg | 29979 |
rs10114717 | snp | A/G | 0.278664 | 0.248351 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83666830 | CAATACATGAACTAT[A/G]TAACATGGCTTGCTT | 29979 |
rs10116424 | snp | C/T | 0.277867 | 0.248442 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83690050 | tataaatcagtacat[C/T]ttggaataacatttt | 29979 |
rs10119441 | snp | C/T | 0.408359 | 0.193449 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83683280 | agccgggcgtgatgg[C/T]gagtgcctatagtcc | 29979 |
rs10121045 | snp | C/T | 0.281313 | 0.248031 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83675615 | CACTTAACTGTGCAA[C/T]TGAGGAGCTACTACC | 29979 |
rs10122131 | snp | A/C | 0.277334 | 0.248501 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83686489 | AAGAAATGATTATTA[A/C]TTCATCTCTAACACA | 29979 |
rs10122134 | snp | C/G | 0.2776 | 0.248472 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83686511 | TCTAACACAAAGGTC[C/G]TACTATAGGTGCACA | 29979 |
rs10125432 | snp | C/T | 0.355954 | 0.226437 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83689984 | AAGACTGTTAAAGAG[C/T]GTTACAGAGGATGCA | 29979 |
rs10125987 | snp | C/T | 0.2768 | 0.248559 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83665795 | TGACTTCTCTTTTGT[C/T]GTTTTAAATAATAAA | 29979 |
rs10217326 | snp | A/G | 0.407845 | 0.193868 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83693510 | TTGTCTTGAAAGCAT[A/G]CCTTCTTTCTCCCCT | 29979 |
rs10283540 | snp | C/G | 0 | 0 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83673921 | aatcctcccacctca[C/G]cctcccaagtagctg | 29979 |
rs10481737 | snp | A/G | 0.407158 | 0.194426 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83678740 | taatttttttgagac[A/G]gagtcttgctttgtc | 29979 |
rs10481738 | snp | A/G | 0.292523 | 0.246357 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83678880 | ccgccaccacgcccc[A/G]ctaatttttttttgt | 29979 |
rs10512137 | snp | A/C | 0.450483 | 0.149354 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83668733 | GAACATTGTTCTGAC[A/C]AATTCCCGTCTTTAA | 29979 |
rs10541629 | in-del | -/TT | 0.164546 | 0.234942 | intron-variant, utr-variant-3-prime | UBQLN1 | GRCh38.p7 | 9:83667911 | CTAGTACTAGCAACA[-/TT]TTGTTTTAGAGTAAA | 29979 |
rs10580448 | in-del | -/TA | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83691210 | ATACATATATATATA[-/TA]TGCCTCATCTTGGGC | 29979 |
rs10642853 | in-del | -/A | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83663080 | GAAAGAAAAAAAAAA[-/A]AAGGGAAAGGCAAAG | 29979 |
rs10712610 | in-del | -/T | 0.0372196 | 0.131242 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83665371 | CCATCATGAAAGCCA[-/T]TTCCATAATGGAAGA | 29979 |
rs10746717 | snp | A/C | 0.473359 | 0.112298 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83675816 | AACAGATGAACTTTG[A/C]AATTCTGGTAAACAG | 29979 |
rs10746718 | snp | A/G | 0.227959 | 0.249026 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83696868 | ATATAATCACAAAAT[A/G]TTATCAGAGATTATA | 29979 |
rs10746719 | snp | C/T | 0.355311 | 0.226737 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83699800 | GCTCTACCAGCCACA[C/T]GGTCTATTCTGAAAG | 29979 |
rs10746720 | snp | A/G | 0.354881 | 0.226936 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83699849 | AAGCAAATGGGCACA[A/G]TAGATTTCGACTACC | 29979 |
rs10780622 | snp | A/C | 0.473359 | 0.112298 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83675920 | AAAATATTGTAACTA[A/C]ATATTACCAATTTTT | 29979 |
rs10780623 | snp | C/T | 0.473634 | 0.111748 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83678802 | GTTCACTGCAAGCTC[C/T]GCCTCCCGGGTTCAC | 29979 |
rs10780624 | snp | C/T | 0.452473 | 0.146644 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83699649 | TGAGCCCAGCTCACA[C/T]TGTATTTCTATAAAA | 29979 |
rs10780625 | snp | G/T | 0.473726 | 0.111565 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83702788 | TATACAGTATAACGT[G/T]AAATCATGTGTGTGA | 29979 |
rs10868037 | snp | A/G | 0.471196 | 0.1165 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83664899 | ACTCATAGCCTAGGC[A/G]AAGGGCGAGACCCTG | 29979 |
rs10868038 | snp | C/T | 0.471388 | 0.116136 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83676764 | GCATCTTTTAAAACA[C/T]GCCCAGTCTATCTCA | 29979 |
rs10868039 | snp | A/G | 0.40853 | 0.193309 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83683344 | gtgaacccaggaggc[A/G]gagcttgcagtgagc | 29979 |
rs10868040 | snp | A/G | 0.355311 | 0.226737 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83687513 | TGGATCTCAACAGAT[A/G]AGGAAATTGCTGCCA | 29979 |
rs10868042 | snp | A/T | 0.471004 | 0.116864 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83693357 | CTGAATGTAATTTTA[A/T]CTTTTGATAATGCTG | 29979 |
rs10868043 | snp | A/G | 0.473359 | 0.112298 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83694726 | AAAACTCAATTCACC[A/G]GTGAACAAAAGGCTG | 29979 |
rs10868044 | snp | C/T | 0.355096 | 0.226837 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83695016 | AATGAGCTAGTTCTA[C/T]ATGGAAAGACTACCA | 29979 |
rs10868045 | snp | A/G | 0.228842 | 0.249103 | intron-variant, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83705876 | CACACAGTACTATAG[A/G]CTCTATGGGATCCCA | 29979 |
rs11140202 | snp | C/T | 0.473451 | 0.112115 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83665567 | TTTACCAGTAAGGTA[C/T]ACTCTAAAACAACAG | 29979 |
rs11140203 | snp | C/G | 0.029116 | 0.117091 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83670401 | TTTTTTCACATCCTA[C/G]AGTCCAACCTTGGAG | 29979 |
rs11140207 | snp | A/C | 0.256061 | 0.249927 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83673568 | AAAAAAAAAAAAAAA[A/C]AAAAAAAAAAAACTG | 29979 |
rs11140209 | snp | G/T | 0.479744 | 0.0985793 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83674959 | CTTAGTTGGACATAT[G/T]TTCAAAGCATATAAA | 29979 |
rs11140210 | snp | C/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83678836 | CATTCTCCTGCCTCA[C/G]CCTCCCGAGTAGCTG | 29979 |
rs11140211 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83679043 | cactgttttggacca[A/G]cctcctgcactatgc | 29979 |
rs11140212 | snp | C/T | 0.45198 | 0.147323 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83682754 | CATTAAAAAGAAAGG[C/T]GCCAACTGATATGTA | 29979 |
rs11140213 | snp | C/T | 0.277067 | 0.24853 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83686569 | CCTAACAATGCATTG[C/T]TTCCCAATATCCTTA | 29979 |
rs11140214 | snp | A/C | 0.406986 | 0.194565 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83688667 | GGAGATAGAGAACAT[A/C]TTGGCCAACATGGTG | 29979 |
rs11140215 | snp | C/G | 0.0275645 | 0.114116 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83694547 | AACACGTATGAGAAA[C/G]GGGCACTCTCTCATA | 29979 |
rs11140216 | snp | C/T | 0.354665 | 0.227036 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83697408 | atacaaaaaattagc[C/T]gggtgtggtggtgtg | 29979 |
rs11140217 | snp | A/T | 0.0275645 | 0.114116 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83699034 | TATTCCACTTATATG[A/T]AATACCTAGAGTAGT | 29979 |
rs11140218 | snp | C/G | 0.0138799 | 0.0821421 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83699534 | GGTCTCGAACTCCAG[C/G]AGGTGGGGGCTGCAG | 29979 |
rs11140219 | snp | C/G | 0.0279526 | 0.114869 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83701989 | TTCGGCAATAAAAAG[C/G]AAGTAAGTACCGGCA | 29979 |
rs11140220 | snp | C/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83704057 | GAAAACGGAATTTGT[C/G]TGATACAGAGCATAA | 29979 |
rs11140221 | snp | C/T | 0.473451 | 0.112115 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83704219 | ATTTTTAATGACAAA[C/T]TTTCATTTGTAACAA | 29979 |
rs11312351 | in-del | -/A | 0.348134 | 0.229934 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83696646 | TCTGTCTAAAAAAGG[-/A]AAAAAAAAAAAATCC | 29979 |
rs11337638 | in-del | -/A | 0.397633 | 0.201754 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83695621 | GAGCTTTAAAGAGTT[-/A]AAAAAAAAAATTACC | 29979 |
rs11393859 | in-del | -/T/TT | 0 | 0 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83678039 | TTTTTTTTTTTTTTT[-/T/TT]GAGACGGAGTCTCGC | 29979 |
rs11403634 | in-del | -/A | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83674186 | TTAAAAAAAAAAAAA[-/A]TAACCAGTATATACC | 29979 |
rs11404740 | in-del | -/T | 0.355311 | 0.226737 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83694386 | TAGTATTTGAAAAAA[-/T]GTCCATAAATCATCC | 29979 |
rs11418417 | in-del | -/A/AA | 0.45946 | 0.136478 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83703169 | ACCAAAAAAAAAAAA[-/A/AA]TCTCATACACAGGGA | 29979 |
rs11560627 | snp | G/T | 0.0287284 | 0.116357 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83672486 | TGACCCAATTTCAAT[G/T]TTGTGTCTCAGAGAA | 29979 |
rs11789565 | snp | A/T | 0.16846 | 0.236329 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83695945 | CTTCACTTTTCAAAT[A/T]AAtttttttttttga | 29979 |
rs11790157 | snp | G/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83697283 | ataggccaggcgcgg[G/T]ggctcacgcctgtaa | 29979 |
rs11790169 | snp | G/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83697430 | ggtggtgtgcacctg[G/T]aatcccagctactca | 29979 |
rs11791379 | snp | A/T | 0.16846 | 0.236329 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83695947 | TCACTTTTCAAATTA[A/T]tttttttttttgagt | 29979 |
rs11792047 | snp | A/C | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83697432 | tggtgtgcacctgta[A/C]tcccagctactcagg | 29979 |
rs12001362 | snp | C/G | 0 | 0 | intron-variant, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83706144 | AAAAACGTAAAAAAT[C/G]AAGTTGAACTTAGGC | 29979 |
rs12115755 | snp | C/T | 0.0807149 | 0.183963 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83694354 | TTTTTGAATTAGCTC[C/T]TTACTCAATATTGCT | 29979 |
rs12115800 | snp | C/T | 0 | 0 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83694921 | CAGATTTCTCCAATT[C/T]TAAGGTTCATGCTCT | 29979 |
rs12235741 | snp | G/T | 0.343701 | 0.231776 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83695388 | TTTTTTTAGTAGAGA[G/T]GGGGTTTCACTATAT | 29979 |
rs12237346 | snp | C/G | 0.5 | 0 | upstream-variant-2KB, intron-variant | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83709618 | TGTGTGTGTGTGTGT[C/G]TGTCTGTCTCCCTGC | 29979 |
rs12238575 | snp | C/G | 0.0275645 | 0.114116 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83695033 | TGGAAAGACTACCAA[C/G]GTAACACAAGTAGAA | 29979 |
rs12238850 | snp | C/T | 0.5 | 0 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83662273 | ATATACATATACATA[C/T]ACACACACACACACA | 29979 |
rs12344615 | snp | A/G | 0.278399 | 0.248382 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83666280 | CAGAGAAGAGCAAGG[A/G]AAAATGTTTATCATC | 29979 |
rs12345514 | snp | G/T | 0.277067 | 0.24853 | upstream-variant-2KB, intron-variant | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83709511 | ACTTCTACTCATCCT[G/T]TATCACATGCCCCAG | 29979 |
rs12346234 | snp | A/C/G | 0 | 0 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83684870 | GATGATACCAGATAA[A/C/G]AGTTTTGAATGCCAC | 29979 |
rs12346707 | snp | A/G | 0.408017 | 0.193729 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83703254 | ggttgagcatcccca[A/G]tccaaaaatatgaaa | 29979 |
rs12551985 | snp | A/C | 0 | 0 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83686917 | ccaaaatccaaaaaa[A/C]caaaaaaagaaaaaa | 29979 |
rs13294533 | snp | C/T | 0.29175 | 0.246489 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83691030 | gcaatcccagctact[C/T]gggaggctaaggcac | 29979 |
rs13301627 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83671229 | ggcatccatgaggga[A/C]agaacaaacttcttc | 29979 |
rs13301769 | snp | C/T | 0 | 0 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83671299 | tgaattaggaacgtt[C/T]ttaatgacattgaga | 29979 |
rs13301873 | snp | G/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83671194 | gtcccctcctccata[G/T]aagtcttgaacccct | 29979 |
rs17080575 | snp | C/T | 0.345482 | 0.231048 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83704499 | ACCATCAGAAAAGGC[C/T]ACTTCAGAAAGACTT | 29979 |
rs17086543 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant, utr-variant-3-prime | UBQLN1 | GRCh38.p7 | 9:83667759 | TTACCTGAGTGCTTA[C/T]ACCACAAGTTTTTAC | 29979 |
rs17086544 | snp | G/T | 0.155987 | 0.23165 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83669417 | TGCACTGTGTTTAAT[G/T]TCACCAAGTACAAAT | 29979 |
rs17086566 | snp | A/T | 0.155987 | 0.23165 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83676863 | CACTATGGCTAATGA[A/T]CTTGGACCTAATTCA | 29979 |
rs17086576 | snp | C/T | 0.0648419 | 0.167978 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83690445 | TTGCAAGTGACTTCT[C/T]GGGAGTTGGTATCAT | 29979 |
rs17853915 | snp | G/T | | | missense | UBQLN1 | GRCh38.p7 | 9:83679881 | TGTCTCATCAGGTCA[G/T]GATTTGAGAGCATGC | 29979 |
rs17853916 | snp | C/T | | | synonymous-codon | UBQLN1 | GRCh38.p7 | 9:83669212 | GTCAGGATTCTGGCT[C/T]AGTGACTGCATCATG | 29979 |
rs17857190 | snp | C/T | 7.47915e-05 | 0.00611475 | missense, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83707607 | CAGCGGCCGCGGGGG[C/T]GCCAGCACCTTCGGC | 29979 |
rs28362654 | snp | A/G | 0.0135176 | 0.0810931 | upstream-variant-2KB, intron-variant | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83708700 | CATCGTAGCAGCAGA[A/G]GCCACTGTCAATACA | 29979 |
rs28555298 | snp | A/G | 0.278399 | 0.248382 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83705318 | CAATCTCGGCTCACT[A/G]TAACCTCCCTCTCCC | 29979 |
rs33950155 | in-del | -/T | 0.278664 | 0.248351 | utr-variant-3-prime | UBQLN1 | GRCh38.p7 | 9:83661618 | TCCAGAAAAGAAAAA[-/T]ACAGAAAAACCCACA | 29979 |
rs33975861 | in-del | -/C | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83682506 | AAACAAACAAACAAA[-/C]AAAAACTAATATAAG | 29979 |
rs34015066 | in-del | -/T | 0.174288 | 0.23826 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83688389 | TATCCAGATTAACTA[-/T]TTTTTCATATGCAAA | 29979 |
rs34137474 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83678774 | CAGGCTGGAGTGCAG[C/T]GGCATGATCTTGGTT | 29979 |
rs34185328 | in-del | -/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83690483 | TTTCTCGACCTTTAG[-/G]CTAAAACACGAACCT | 29979 |
rs34407853 | in-del | -/A | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83690746 | TCTCAAAAAAAAAAA[-/A]CAAGAACAGAAACAT | 29979 |
rs34702839 | in-del | -/C | | | utr-variant-3-prime | UBQLN1 | GRCh38.p7 | 9:83660656 | TCAAGGACAGATTCC[-/C]GCTGCCCCACCCCCC | 29979 |
rs34795460 | in-del | -/A | 0.45235 | 0.146814 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83685155 | CACCAAAATAGAAGG[-/A]AATATGTTGAATGAG | 29979 |
rs34821277 | in-del | -/A/AA | 0 | 0 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83698928 | AAAAAAAAAAAAAAA[-/A/AA]GTAAATTCTGACACA | 29979 |
rs34922735 | in-del | -/C | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83694135 | ATTCTCCATCTCACC[-/C]TATTAAACATCCGGG | 29979 |
rs35057345 | in-del | -/C | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83686718 | ACAGTATACACAGCC[-/C]AATCTCATATTCTTG | 29979 |
rs35319221 | in-del | -/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83697734 | CTATTTTTTGTACCC[-/T]TTTTTTTTTTTTTTT | 29979 |
rs35326751 | in-del | -/C | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83680340 | AACTTTGGAATTTTC[-/C]TGAGTGACAGGAGTA | 29979 |
rs35476718 | in-del | -/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83695958 | TTAATTTTTTTTTTT[-/T]GAGTCGGAGTCTCAC | 29979 |
rs35505951 | in-del | -/T | 0 | 0 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83693467 | TTCTTATTTTTTTTT[-/T]AACCAGACTGTCAAG | 29979 |
rs35535452 | snp | C/T | 0.2776 | 0.248472 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83684488 | GTGTGAGCCACCGCG[C/T]CTGGCCTGATTATTA | 29979 |
rs35561015 | in-del | -/C | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83693708 | ACTTTGCTTACTCCC[-/C]TGTTCTCAATTGTTT | 29979 |
rs35570246 | in-del | -/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83679282 | TTCTTCAGCCCTTTT[-/T]ATGCCTATAAAGCCA | 29979 |
rs35592945 | in-del | -/A | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83682503 | AACAAACAAACAAAC[-/A]AAAAAAACTAATATA | 29979 |
rs35656702 | in-del | -/G | 0.292523 | 0.246357 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83676009 | CATTTTGCCTCTTGG[-/G]CCAGTAATACCTGAA | 29979 |
rs35877566 | in-del | -/T | 0.278664 | 0.248351 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83704517 | TCAGAAAGACTTTAA[-/T]TTTTATCTATTAACA | 29979 |
rs35957755 | in-del | -/CAAA | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83682498 | AAAAAAACAAACAAA[-/CAAA]CAAACAAAAACTAAT | 29979 |
rs35972410 | in-del | -/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83695569 | TAAAAGGTATTTTTT[-/T]AAATGTAAAAGTTAT | 29979 |
rs35985618 | in-del | -/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83668655 | CAAATTAGAAAAAGG[-/G]AATACATTAATAAGG | 29979 |
rs36072668 | in-del | -/T | 0.498059 | 0.0310896 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83695216 | CTTTTTTTTTTTTTT[-/T]GAGACTAAGTCTCAC | 29979 |
rs36087147 | in-del | -/AGATAAG | 0.407674 | 0.194008 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83684864 | CTTCCAGATGATACC[-/AGATAAG]GAGTTTTGAATGCCA | 29979 |
rs36096614 | in-del | -/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83694387 | AGTATTTGAAAAAAG[-/T]TCCATAAATCATCCA | 29979 |
rs41282415 | snp | A/G | | | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83708070 | GAGCTCAGCCTGCGT[A/G]CCTTTTCCTTTCCCG | 29979 |
rs41308878 | snp | C/T | 0.190833 | 0.242898 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83679012 | AAGCGTGAGCCACCG[C/T]GCCCGGCCAGGAGGC | 29979 |
rs41309243 | snp | A/G | 0.190519 | 0.242821 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83678923 | AGACGGGGTTTCACC[A/G]TGTTAGCCAGGATGG | 29979 |
rs55649824 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant, nc-transcript-variant | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83708389 | ATCGCCTTGCCCTCC[C/T]TTGCCTCTCTGTCTA | 29979 |
rs55710609 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83696517 | GGTGGTGCACGCCTG[C/T]AGTCCCAGTTTCTTC | 29979 |
rs56098781 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83683717 | ACCCACAAAGCTTGA[C/T]TATATAAAAAACTTT | 29979 |
rs56213838 | snp | C/T | | | missense | UBQLN1 | GRCh38.p7 | 9:83683025 | GATGTAGTAACATTG[C/T]TTCCAGCTGTATTTG | 29979 |
rs56365898 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83696536 | CCCAGTTTCTTCAGA[A/G]GCTGAAGTGGGAGAA | 29979 |
rs56400725 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83682581 | TTCCATGTGTTCAGG[A/G]CAGTTACAAAATAAC | 29979 |
rs56889142 | in-del | -/A | 0.5 | 0 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83675483 | AAAAAAAAAAAAAAA[-/A]TCACAAGAAGCAAGA | 29979 |
rs56928462 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83691406 | CTGTAATCTCAAAAT[C/T]TAATAGAACAGCAAT | 29979 |
rs57071190 | snp | C/T | 0.0655868 | 0.168795 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83669049 | ACACGGTCTAAAAAA[C/T]TGGAGACACAGTTTA | 29979 |
rs57150962 | in-del | -/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83682825 | ATGTTTTTTTTTTTT[-/T]AATTTTTGTTGTTAA | 29979 |
rs57176325 | in-del | -/T | | | intron-variant, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83706957 | TCATAATTTTTTTTT[-/T]AAAGGTTGCAAGGTG | 29979 |
rs57338929 | snp | G/T | 0.0810805 | 0.184299 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83703102 | TCTAGATGTTATCTT[G/T]CTCGTGGATACTTGG | 29979 |
rs57391609 | snp | A/C | 0.0810805 | 0.184299 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83701468 | GTTTCATCTCATGGT[A/C]CCCTTAACAGGGTAT | 29979 |
rs57550660 | in-del | -/TT/TTTTTTTTTTTTT | 0 | 0 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83705257 | CTCCTTTTTTTTTTT[-/TT/TTTTTTTTTTTTT]GAAACGGAGTTTCAC | 29979 |
rs59017415 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83673355 | ACCAGCCTGGCCAAC[A/G]TGGTGAAACACTGTC | 29979 |
rs59776869 | in-del | -/C/CTA | | | intron-variant, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83705872 | ATACACACAGTACTA[-/C/CTA]TAGGCTCTATGGGAT | 29979 |
rs59851611 | snp | C/T | 0.0810805 | 0.184299 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83703909 | ATTACCACCTTACAA[C/T]TTACCCAAGAAGTTT | 29979 |
rs60734573 | snp | A/T | 0.0818113 | 0.184966 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83662102 | CATATTTAAAAGTCC[A/T]TTAGCAGTTTATTTT | 29979 |
rs61162738 | snp | C/T | 0.0376037 | 0.131863 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83675417 | TTTTGACAACTAAAA[C/T]TGTTTGAATCACAAG | 29979 |
rs61218358 | snp | G/T | 0.0810805 | 0.184299 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83703765 | GAAAAAAGCTTAAGC[G/T]TTATTAGTAACCTTG | 29979 |
rs61270284 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83696560 | GGGAGAATCGCTTGA[A/G]CCCAGGAGATCAAGG | 29979 |
rs61528776 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83674240 | AACAAGAAAAAAGGA[A/G]GAAGGAGAGTTACAA | 29979 |
rs61567557 | snp | C/T | 0.0810805 | 0.184299 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83699861 | ACAATAGATTTCGAC[C/T]ACCAGTTTGCTGGCC | 29979 |
rs62559843 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83670314 | TCACTTATCTTTCTA[A/G/T]TTTATTATAATTCTG | 29979 |
rs62559844 | snp | A/T | 0.5 | 0 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83674184 | AAAATCACTGCAGCA[A/T]TAAAAAAAAAAAAAT | 29979 |
rs62559845 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83681477 | TCACAGGATATTATG[A/G]TAATATAACCCAAGT | 29979 |
rs62559846 | snp | G/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83697244 | GTCTCAGTATCTTCT[G/T]GTTTTTTTTTTTTTT | 29979 |
rs62559847 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83697496 | GGCGGAGGTTGCAGT[A/G]AGCTGAGATTGCACC | 29979 |
rs62559848 | snp | G/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83701679 | GTAATAAGTATTACC[G/T]AGAATGTGGTTATCG | 29979 |
rs71365321 | in-del | -/AT | 0 | 0 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83682305 | TATATATATATATAT[-/AT]TCCACAGAACCTCAA | 29979 |
rs71365322 | in-del | -/T | 0.475702 | 0.107512 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83697246 | TTTTTTTTTTTTTTT[-/T]AAGACATAGGCCAGG | 29979 |
rs71498070 | in-del | -/GT/GTGT/TC | 0.5 | 0 | upstream-variant-2KB, intron-variant | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83709587 | TGTGTGTGTGTGTGT[-/GT/GTGT/TC]CTGTCTCCCTGCATT | 29979 |
rs71502717 | snp | A/T | 0.5 | 0 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83663143 | GGGAAGAGGAAAGGG[A/T]AAAGGGAAAGGGGAA | 29979 |
rs71502718 | snp | C/T | 0.5 | 0 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83704709 | GCATGCGCCTGTAGT[C/T]TCAGCTACTAGGGAA | 29979 |
rs72074805 | in-del | -/GT/TG | | | upstream-variant-2KB, intron-variant | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83709589 | ATACCGTGTGTGTGT[-/GT/TG]GTGTGTGTGTGTGTG | 29979 |
rs72414554 | in-del | -/TC/TT | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83705247 | GAAGCCAGCACTCCT[-/TC/TT]TTTTTTTTTTGAAAC | 29979 |
rs72454301 | in-del | -/AT | 0.0372196 | 0.131242 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83702794 | GTATAACGTTAAATC[-/AT]GTGTGTGATGATGAC | 29979 |
rs72618136 | snp | A/G | 0.473543 | 0.111932 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83684487 | GGTGTGAGCCACCGC[A/G]CCTGGCCTGATTATT | 29979 |
rs72746868 | snp | C/T | 0.191461 | 0.24305 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83682866 | AAGTGACATAATGTT[C/T]TATTTTCTCATTTTA | 29979 |
rs72746869 | snp | C/G | 0.17654 | 0.238964 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83686375 | CCAGCCTGGGTGACA[C/G]AGTGATATCCCGCCT | 29979 |
rs72746870 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83689177 | ATATTATAACATATG[A/G]TCTTTGTGACTAGCT | 29979 |
rs72746871 | snp | C/T | 0.174288 | 0.23826 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83689194 | CTTTGTGACTAGCTT[C/T]TTATACTTGGCATGT | 29979 |
rs72746877 | snp | A/G | 0.5 | 0 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83696644 | ATTCTGTCTAAAAAA[A/G]GAAAAAAAAAAAAAT | 29979 |
rs72746879 | snp | A/C | 0.175897 | 0.238765 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83700863 | ACTCCATTATATATT[A/C]TAAGACCAACAGGGA | 29979 |
rs72746880 | snp | C/T | 0.192401 | 0.243274 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83701024 | GGTAATGGCAACTTA[C/T]TGGAGCCACTACCCG | 29979 |
rs72746881 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83701840 | AAAATGAAAACGTTA[C/T]GTCCCCACAAAAACT | 29979 |
rs72746882 | snp | A/G | 0.191775 | 0.243125 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83703581 | CAAGCATTTCCCATA[A/G]GGGATACTCAAAACC | 29979 |
rs73476336 | snp | C/T | 0.02016 | 0.0983543 | utr-variant-3-prime | UBQLN1 | GRCh38.p7 | 9:83660393 | TGAACCAGAGTCAGC[C/T]AAATGTATCACTGAC | 29979 |
rs73476338 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83663434 | CTACCGCAGGAGGTG[A/G]TGTCATGGGTGGAGT | 29979 |
rs73476342 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83664137 | ATAAGCTAAGCCATC[C/T]TCTTAAAATAAGCCC | 29979 |
rs73476345 | snp | A/C | 0.0178098 | 0.0926698 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83665207 | GAACGTAAATTTTTA[A/C]ATCTTTTCTCTGTTA | 29979 |
rs73476376 | snp | A/C | 0.02016 | 0.0983543 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83676621 | GATATCCACTGTATT[A/C]TATAAAAGAATATAT | 29979 |
rs73478129 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83705539 | TGAGCCACCGCATCC[A/G]GCCCAGAAGCATTTT | 29979 |
rs73478135 | snp | A/C | 0.0221141 | 0.102801 | upstream-variant-2KB, intron-variant | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83708942 | GAATCCTAATTTGAA[A/C]TGACGTCATTGGCTT | 29979 |
rs73648569 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, downstream-variant-500B | UBQLN1 | GRCh38.p7 | 9:83667071 | TTAAGACCTAAAAGA[C/T]GTAAATCCATTTGAG | 29979 |
rs73648570 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83682826 | TATAGGAATGTATGT[G/T]TTTTTTTTTTAATTT | 29979 |
rs74332669 | snp | C/T | 0.0810805 | 0.184299 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83689255 | TCAATACTTCATCCC[C/T]TTCTATGGCCAAATA | 29979 |
rs74625510 | snp | A/G | 0.0287284 | 0.116357 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83671800 | GACACATTAGCCCCA[A/G]CAGTCAGCCTTTCCT | 29979 |
rs74698781 | snp | A/G | 0.5 | 0 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83684834 | AAAAAAAAAAGTAAG[A/G]AAATAAAAAAAACCC | 29979 |
rs74780193 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83664400 | CTCCAGTCTGCTCGA[C/T]GGAGTGAGACTATCT | 29979 |
rs74876378 | snp | C/G | 0.0275645 | 0.114116 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83686835 | AGGAAATGCTCATTG[C/G]AGCATTTTCCAACTT | 29979 |
rs74901315 | snp | C/T | 0.1652 | 0.235179 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83675665 | ATCTGAATGTAATGG[C/T]ATGTTAAAAACAACA | 29979 |
rs75034037 | snp | A/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83685729 | TTTCCTTACTAAAAG[A/T]AAAGCTAAAAACTTG | 29979 |
rs75229502 | snp | A/G | 0.155987 | 0.23165 | intron-variant, utr-variant-3-prime | UBQLN1 | GRCh38.p7 | 9:83668159 | GTACCTCCAATATAC[A/G]GAATCACAGACACAA | 29979 |
rs75250712 | snp | C/T | 0.0287284 | 0.116357 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83675436 | TTGAATCACAAGCAA[C/T]GTCAAGGTGCTTTAC | 29979 |
rs75720080 | snp | A/C | 0.5 | 0 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83684810 | AGTGAAATTCCGTCT[A/C]AAAAAAAAAAAAAAA | 29979 |
rs75734183 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83698626 | AGTCATACACAGTAA[A/G]TTCTGGCTGGGTGCG | 29979 |
rs75802466 | snp | A/T | 0.0640965 | 0.167152 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83674340 | CAATGACACTAAAAG[A/T]ATACAACATATATAA | 29979 |
rs75865570 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83662522 | ATTTCAGCAGCATCA[A/T]ATCTTTTCTTCAGAA | 29979 |
rs75905735 | snp | A/G | 0.5 | 0 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83696646 | TCTGTCTAAAAAAGG[A/G]AAAAAAAAAAAATCC | 29979 |
rs75926331 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83703050 | AACTCCCCTCCATTA[C/T]CTGCACTAATGTCTC | 29979 |
rs75981873 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83685662 | AAAGAAATATGATTA[G/T]CAATTCGTGGTTTGC | 29979 |
rs76011942 | snp | G/T | 0.5 | 0 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83678040 | TTTTTTTTTTTTTTT[G/T]AGACGGAGTCTCGCT | 29979 |
rs76012363 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83709406 | TCCTCATTACCTGTT[C/T]TTCCCTGTCATGCTG | 29979 |
rs76049168 | snp | A/C | 0 | 0 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83684813 | GAAATTCCGTCTCAA[A/C]AAAAAAAAAAAAAAA | 29979 |
rs76213075 | snp | C/T | 0.0142736 | 0.0832652 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83708071 | AGCTCAGCCTGCGTG[C/T]CTTTTCCTTTCCCGC | 29979 |
rs76252755 | snp | A/C | | | intron-variant, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83706133 | AATTACGTCAAAAAA[A/C]CGTAAAAAATGAAGT | 29979 |
rs76265103 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83695076 | AGAAAATTGTGGGTG[G/T]TTGACCCCATTTGCT | 29979 |
rs76390231 | snp | C/G/T | 0.00358779 | 0.0422022 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83685332 | CTGTATGAAAAAATA[C/G/T]GGACACTGACAACTA | 29979 |
rs76468130 | snp | C/T | 0.0810805 | 0.184299 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83694167 | AGTTGGGAATCAACC[C/T]ATCCAAAAGTAAAAT | 29979 |
rs76505924 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83687574 | TCTTCTGGTTGTCAC[A/G]ATAAACGGAAAGACA | 29979 |
rs76689059 | snp | A/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83695621 | GAGCTTTAAAGAGTT[A/T]AAAAAAAAAATTACC | 29979 |
rs76770883 | snp | C/T | 0.0810805 | 0.184299 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83670310 | CTTCTCACTTATCTT[C/T]CTAGTTTATTATAAT | 29979 |
rs76923905 | in-del | -/T | 0.473266 | 0.112482 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83675930 | ACTAAATATTACCAA[-/T]TTTTTTTATTTTTTC | 29979 |
rs77214744 | snp | A/C | 0.5 | 0 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83670553 | TCGGTCTAAAAAAAA[A/C]CTCTGCACATAAATA | 29979 |
rs77222674 | snp | C/G | 0.0287284 | 0.116357 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83671564 | CACTGTCAATGAGCA[C/G]TAATATTTTGAAAGG | 29979 |
rs77247588 | snp | A/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83682837 | ATGTTTTTTTTTTTT[A/T]ATTTTTGTTGTTAAA | 29979 |
rs77359731 | snp | A/G | 0.0275645 | 0.114116 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83699234 | GAACCCTTAAAAATG[A/G]TTAACATGATAAATT | 29979 |
rs77401823 | snp | A/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83663444 | AGGTGGTGTCATGGG[A/T]GGAGTTAAGGTAGTT | 29979 |
rs77515396 | in-del | -/AAAA | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83673577 | AAAAAACAAAAAAAA[-/AAAA]CTGCGCTTACGTTTT | 29979 |
rs77539237 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83698159 | AAATATTGGCCATTA[C/T]GTCATTGTCATTAAC | 29979 |
rs77665820 | snp | C/G/T | 0.0810805 | 0.184299 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83701993 | GCAATAAAAAGGAAG[C/G/T]AAGTACCGGCACATG | 29979 |
rs77949543 | snp | A/T | 0 | 0 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83674186 | AATCACTGCAGCATT[A/T]AAAAAAAAAAAATAA | 29979 |
rs77969318 | snp | C/T | 0.141596 | 0.225274 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83698027 | CAGCATGAGCCACCA[C/T]GCCTGGCCAGCATCT | 29979 |
rs78121419 | snp | C/T | 0.0821764 | 0.185298 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83680744 | AACATAAGTGTTTCC[C/T]TGAGTTCTAGGTGCC | 29979 |
rs78155052 | snp | A/C | 0.0279526 | 0.114869 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83686756 | GGTGGAGTATCTCTA[A/C]TGCAAATACCCCAAA | 29979 |
rs78178276 | snp | C/T | 0.0785177 | 0.181917 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83687809 | TCTGTTTTACCTTTG[C/T]CAACTCCCATACACA | 29979 |
rs78326037 | snp | C/G | 0.0821764 | 0.185298 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83673721 | TCATTCTCACTTATT[C/G]TCTATGGGTGTTTTG | 29979 |
rs78531074 | snp | C/T | 0.0810805 | 0.184299 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83701728 | AGTGGAAATGTAAAA[C/T]GGTACAGACACCTTA | 29979 |
rs78549631 | snp | C/G | 0.0298908 | 0.118541 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83685135 | GTTACCATGTATTCA[C/G]AATAGCACCAAAATA | 29979 |
rs78624564 | snp | A/T | 0 | 0 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83694386 | ATAGTATTTGAAAAA[A/T]GTCCATAAATCATCC | 29979 |
rs78647381 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83682825 | TTATAGGAATGTATG[G/T]TTTTTTTTTTTAATT | 29979 |
rs78676059 | snp | C/G | 0.0752113 | 0.178743 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83688214 | TAGCTACTACTATGC[C/G]AGTTCTCTTAATACT | 29979 |
rs78676275 | snp | G/T | 0.0275645 | 0.114116 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83699092 | TGGTTGCTAGAGGTG[G/T]GGGAATGGGGAAAAT | 29979 |
rs78714386 | snp | A/C | 0.344147 | 0.231595 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83697648 | GCAACCTCTGCCTCG[A/C]AGATTCAAGAGATTC | 29979 |
rs78836058 | snp | G/T | 0.5 | 0 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83678038 | CTTTTTTTTTTTTTT[G/T]TGAGACGGAGTCTCG | 29979 |
rs79044117 | snp | C/T | 0.5 | 0 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83670554 | CGGTCTAAAAAAAAA[C/T]TCTGCACATAAATAT | 29979 |
rs79054011 | snp | A/T | 0.00676609 | 0.0577691 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83676808 | CTCCCATGTCTCCAT[A/T]TCTTCCTACTTATAC | 29979 |
rs79058106 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83663442 | GGAGGTGGTGTCATG[A/G]GTGGAGTTAAGGTAG | 29979 |
rs79083353 | snp | G/T | 0.0785177 | 0.181917 | intron-variant, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83706339 | TTCAACTTTCCGCAT[G/T]CTTGAAAATACAAAA | 29979 |
rs79165801 | snp | A/C | 0.0785177 | 0.181917 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83693582 | TAAGAGAAGTTAGAA[A/C]ACCGTATCAAATAAG | 29979 |
rs79167512 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83669556 | ACATTCTGCATTTAC[A/C]GTAAAATCTTGTCTA | 29979 |
rs79268870 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83690393 | GTTGGGGACAAAATC[C/T]ATGGTGCCCAAAGTG | 29979 |
rs79445841 | snp | C/T | 0.0287284 | 0.116357 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83671764 | AATAATAAATGAGCA[C/T]TGGCTTCAACTCAGT | 29979 |
rs79530639 | snp | A/G | | | missense | UBQLN1 | GRCh38.p7 | 9:83661923 | TGTTGCTGAAATCTG[A/G]CTTCTGGATTCTGTA | 29979 |
rs79600395 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83681077 | AATCTTTCCAAAAGA[A/C]TAGTTTAAGTTTTAT | 29979 |
rs79601025 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83679265 | TTTTTGTTCGTTTTT[C/G]CTTTCTTCAGCCCTT | 29979 |
rs79722629 | snp | A/C | 0.0182019 | 0.0936463 | intron-variant, downstream-variant-500B | UBQLN1 | GRCh38.p7 | 9:83667379 | TGGGGAGGAAATGAT[A/C]CTTGCCCTCAAGAAG | 29979 |
rs79854900 | snp | C/T | 0.0275645 | 0.114116 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83703332 | TGTGGAAAAATCCCA[C/T]ATGTAACACCTTTGC | 29979 |
rs79901564 | snp | C/T | 0.0704125 | 0.17392 | intron-variant, utr-variant-3-prime | UBQLN1 | GRCh38.p7 | 9:83668076 | GCTTATTATGGTAAA[C/T]TGAAGCATTTAATAC | 29979 |
rs79903988 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83670663 | CTTAAAATAAGACAA[C/T]GATGAAGTTTGCCAC | 29979 |
rs79937729 | snp | A/G | 0.0283406 | 0.115616 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83700032 | TTTTTCCTGAAGAAC[A/G]GGTTGATAAACCAGC | 29979 |
rs79938725 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83702136 | ATAGATCAGTAGTTG[C/G]CTAAGGCTGGGGGGC | 29979 |
rs80043240 | snp | A/G | 0.473543 | 0.111932 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83697409 | TACAAAAAATTAGCT[A/G]GGTGTGGTGGTGTGC | 29979 |
rs80063080 | snp | C/T | 0.5 | 0 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83670918 | TCTGTACAAGTTTTT[C/T]CATGGCATTGTAGCA | 29979 |
rs80105634 | snp | A/G | 0.0821764 | 0.185298 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83691711 | CTGACAGACACGTGA[A/G]AAATCACGTTCACTC | 29979 |
rs80201630 | snp | A/C | 0.0182019 | 0.0936463 | intron-variant, downstream-variant-500B | UBQLN1 | GRCh38.p7 | 9:83667506 | GCAGATGTCAGACAA[A/C]CTTTCAGGAACATAC | 29979 |
rs80268574 | snp | C/G | 0.0766824 | 0.180169 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83703666 | TTATATTCTCACTAC[C/G]TATTCTAGCAACCTG | 29979 |
rs80315207 | snp | C/T | 0 | 0 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83682145 | CAAAAATTAGCAGGG[C/T]GTGGTGGCACACGCC | 29979 |
rs80348560 | snp | C/G | 0.0178098 | 0.0926698 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83704144 | GGTACAAATTTTAAA[C/G]ACTAAATATTTCCCA | 29979 |
rs111266506 | snp | A/C/G | 0.0197687 | 0.0974348 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83697503 | GTTGCAGTGAGCTGA[A/C/G]ATTGCACCACTGCAC | 29979 |
rs111323270 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83680400 | ATCATTATGCTAATG[A/G]AGTGACTTAGGCCCC | 29979 |
rs111332281 | snp | C/G | 0.0788843 | 0.182262 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83673526 | CTCCAGCCTGGGTGA[C/G]AGGTCGAGACTCGGT | 29979 |
rs111353216 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83691643 | CCTGGCACCACACAC[A/G]CATTTTCACATTCAC | 29979 |
rs111381991 | snp | A/G | 0.156319 | 0.231784 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83682411 | GTAAGCCAGGAGTTT[A/G]AGGCTGCAGTGAGCT | 29979 |
rs111432692 | snp | A/C | 0.00557542 | 0.0525036 | upstream-variant-2KB, intron-variant | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83709996 | CAGAGTAATCATAGA[A/C]AATACATACATGAAT | 29979 |
rs111470483 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime | UBQLN1 | GRCh38.p7 | 9:83660392 | CTGAACCAGAGTCAG[A/C]CAAATGTATCACTGA | 29979 |
rs111597069 | snp | C/T | 0.444444 | 0.157135 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83691441 | ATAGCTCACTTGAAC[C/T]TCTGGTAACATTTAA | 29979 |
rs111598880 | snp | G/T | 0.0178098 | 0.0926698 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83683207 | CACGAGGTCAAGAGA[G/T]AGAGAACATCCTGGC | 29979 |
rs111607230 | snp | A/T | 0.02016 | 0.0983543 | intron-variant, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83707363 | CCACGAACTTGGGTG[A/T]GATCTAATTTGGGAC | 29979 |
rs111705315 | snp | A/C | 0.5 | 0 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83695686 | ACCAGTAAACCAGGC[A/C]GACTGTTGCCATATC | 29979 |
rs111853809 | snp | C/T | 0.5 | 0 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83662271 | GTATATACATATACA[C/T]ATACACACACACACA | 29979 |
rs111854716 | snp | A/C | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83663393 | CTTTAGCCATATTTA[A/C]GAGATATATATATAT | 29979 |
rs111920179 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83686732 | CCAATCTCATATTCT[C/T]GGCCTAGCGGTGGAG | 29979 |
rs111943360 | snp | C/T | 0.5 | 0 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83666496 | AGTAATGTACCTTGT[C/T]TTATTCTATCTTCCC | 29979 |
rs111966446 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83704371 | GTATCTGTTTCCCTT[A/G]CATATACAAAGCCCA | 29979 |
rs112105058 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83699189 | GTAACAATTGTACAA[C/T]AATGTGAATGTACTT | 29979 |
rs112107390 | snp | A/C | 0.0182019 | 0.0936463 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83690144 | TGTCCACAAAAAATA[A/C]AATCAACATTTGAAC | 29979 |
rs112108138 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83698890 | CTGCACTCCAGCCTG[A/G]GTGACAAAGTGAGAC | 29979 |
rs112109747 | snp | G/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83698482 | TGCACCTTAAAATAT[G/T]TTAGACATACTGGGT | 29979 |
rs112127276 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83697281 | ACATAGGCCAGGCGC[A/G]GTGGCTCACGCCTGT | 29979 |
rs112149026 | in-del | -/A | 0.0821764 | 0.185298 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83692111 | GTTTAGCTGTCTGCC[-/A]CTCTATTTGAAACAA | 29979 |
rs112172395 | snp | A/G | 0.0429648 | 0.14013 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83708225 | GCGCTGTAACGGCGC[A/G]CCGAGATGACGTCAC | 29979 |
rs112272061 | snp | C/T | | | intron-variant, utr-variant-3-prime | UBQLN1 | GRCh38.p7 | 9:83667787 | TACACTCAAGAGTCT[C/T]TTTAAATATTTAAAA | 29979 |
rs112303725 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83706921 | ACTATTACTTAAGAT[A/G]GAGCTAAAAACAGTT | 29979 |
rs112377239 | snp | A/C | 0.5 | 0 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83689789 | TGCAACACAACCAGC[A/C]CAGCTCAAATCCAGA | 29979 |
rs112380370 | snp | A/C | 0.5 | 0 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83680080 | AAATCAAAGTCAGAA[A/C]ATTTATCATTAACAT | 29979 |
rs112413386 | snp | A/G | 0.0648419 | 0.167978 | intron-variant, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83707401 | GGGAGAATGGCCGAG[A/G]ACGACCCCTCTCCCA | 29979 |
rs112424928 | in-del | -/A | 0.5 | 0 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83696468 | AAACAAAAAAATTTT[-/A]AAAAAAAACCCAATA | 29979 |
rs112495101 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83690894 | TGTAATCCCAACACT[C/T]TGGGAGGCCAAGGCG | 29979 |
rs112581718 | snp | C/G | 0.00795532 | 0.062565 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83695265 | GTACAGTGGCGCCAT[C/G]TTGGCTCACTGCAAC | 29979 |
rs112722124 | snp | G/T | 0.0614824 | 0.164198 | intron-variant, utr-variant-3-prime | UBQLN1 | GRCh38.p7 | 9:83668512 | AAAGGGTTATCGGAC[G/T]CAATTATCTCAAAAT | 29979 |
rs112732203 | snp | C/T | 0.5 | 0 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83674790 | TAAGTCTGAAGTGAC[C/T]GGAAAATTACCCTCT | 29979 |
rs112787692 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83664666 | GTCTCTGATCCCACT[C/T]TGGGAGGCCAAATCT | 29979 |
rs112821792 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83686373 | CTCCAGCCTGGGTGA[C/T]AGAGTGATATCCCGC | 29979 |
rs112831334 | snp | A/G | 0.5 | 0 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83663159 | AAAGGGAAAGGGGAA[A/G]AGGAAGGAGGAAAAG | 29979 |
rs112835393 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83695240 | GTCTCACTCTGTCGC[C/T]CAGGCTGGAGTACAG | 29979 |
rs112853959 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83695838 | GTGAAGTATGCTAAT[C/T]CAACAGTCTCTGCAA | 29979 |
rs112880320 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83698752 | AACCCTGTCTCTACA[A/G]AAAAATACAAAGTAG | 29979 |
rs112922648 | snp | A/T | 0.5 | 0 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83679091 | AACCAAAATAGAGCC[A/T]CTTGTGCCAAGTGCC | 29979 |
rs112985825 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | UBQLN1 | GRCh38.p7 | 9:83661268 | AGAGCCTATTGCAGT[A/G]TGTTTCCAGAAATGC | 29979 |
rs112995876 | snp | A/G | 0.5 | 0 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83678195 | CCCAGCTAATTTTTT[A/G]TATTTTTAGTAGAGA | 29979 |
rs113003751 | snp | A/C | 0.5 | 0 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83684158 | GACTTCACCAAAAGA[A/C]AGCCAACAAATCAAT | 29979 |
rs113009464 | snp | G/T | 0.5 | 0 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83688405 | TTTTCATATGCAAAA[G/T]GAGAGGGTAAAACTA | 29979 |
rs113069746 | snp | C/T | 0.5 | 0 | intron-variant, utr-variant-3-prime | UBQLN1 | GRCh38.p7 | 9:83668489 | AGTACCTAGGCAACT[C/T]GAGGGAGAAAGGGTT | 29979 |
rs113354995 | snp | A/C/G | 0.0178167 | 0.0926884 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83678617 | ACGAAAAATATTTCC[A/C/G]AAAAAAGAAAAAAAA | 29979 |
rs113362574 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83662998 | GGAGGATTGCTGCAG[C/T]CCAGGAGGTGCAGGT | 29979 |
rs113389628 | snp | A/G | 0.0777841 | 0.181223 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83705440 | TTTTTAGTAGAGACG[A/G]GGTTTCACCCCGTTG | 29979 |
rs113438853 | in-del | -/CC | 0.155656 | 0.231515 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83693234 | AACAACTTTCAGCAA[-/CC]CCCCATTTTTTTCAA | 29979 |
rs113487437 | snp | G/T | 0.02016 | 0.0983543 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83670745 | AGAACTTTCAAAATT[G/T]GAGCCAATCCTCTCA | 29979 |
rs113509124 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83685743 | GAAAAGCTAAAAACT[C/T]GCCTGTTCTAATGCA | 29979 |
rs113640732 | snp | A/G | 0.0748431 | 0.178382 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83692840 | CTGGGCAACAAGAGC[A/G]GAACTCCGTTTTAAA | 29979 |
rs113661130 | snp | A/C | 0.5 | 0 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83694206 | GCTCTGAAGATAAAA[A/C]ACACACAATTTCATT | 29979 |
rs113757172 | snp | A/C | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83695163 | CCAAAAAAAAAAAAA[A/C]GTTAACTTTACCTTT | 29979 |
rs113897288 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83705873 | ATACACACAGTACTA[C/T]AGGCTCTATGGGATC | 29979 |
rs113921411 | snp | G/T | 0.0418186 | 0.138422 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83707835 | GCCACCGTAGCGGGT[G/T]TGGGGCCCCGGAGCT | 29979 |
rs113949173 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83701605 | TGAAAATAAAAAGCA[A/G]AATAATCACAGTAAG | 29979 |
rs114240617 | snp | A/T | 0.02016 | 0.0983543 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83679021 | CCACCGCGCCCGGCC[A/T]GGAGGCCACTGTTTT | 29979 |
rs114242512 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83700655 | TAAGATTTAAAGATG[A/G]AAAAGGAATGGGCAA | 29979 |
rs114324770 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83698559 | CCAAGCGACCAGCAA[C/T]AGATCAATGGATTTT | 29979 |
rs114417765 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83666561 | GGTAGAACATAAATA[A/G]AAAAAGGAAAAGGGA | 29979 |
rs114577026 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83669710 | ATTAGAATCATATTC[A/G]GCACTTAATATTGCC | 29979 |
rs114651509 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83663003 | ATTGCTGCAGCCCAG[A/G]AGGTGCAGGTCGCAG | 29979 |
rs114701197 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83703031 | TAATTAGAAGTTACA[A/C/T]AGAAACTCCCCTCCA | 29979 |
rs114829901 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83662033 | TGCTTTTTTATAACA[C/T]ATGCTGATCTACTGA | 29979 |
rs114848471 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83704733 | TAGGGAAGCTGGGGT[A/G]GGAGAATCCTTGAAC | 29979 |
rs115046046 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83697137 | GGCAGTTTGGGGCAG[C/T]GGATCGGTGAGGCCT | 29979 |
rs115054183 | snp | A/C/G | 0.00835141 | 0.0640778 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83679147 | GGGCCAGTTTCCCCC[A/C/G]CAAAACCATAGTAAG | 29979 |
rs115098381 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83693747 | AAAATAAGACACACA[A/T]ATGGAGGAAAGAGAG | 29979 |
rs115359734 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83680142 | AGCTGACCCAATAGT[C/T]TATTACAAGAAATCA | 29979 |
rs115370009 | snp | A/G/T | 0.0023933 | 0.0345097 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83664621 | TAAATAAATAAAAAC[A/G/T]GTGGGGGAGAACCAG | 29979 |
rs115409907 | snp | C/T | 0.0810805 | 0.184299 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83697794 | CAGGCTGGAGTGCGA[C/T]GGCACGATTCAGCTC | 29979 |
rs115425709 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83683797 | CGAGGCCGAGGCAGG[C/T]GATCAACTGAGGTCA | 29979 |
rs115700871 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83665983 | TAAAATAGAATAGGG[C/T]AGCTCTTTCCTGTTA | 29979 |
rs116034157 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83699888 | GGCCTCTGCCCTAAG[A/G]CACCCATTATAAGCA | 29979 |
rs116074610 | snp | C/G | 0.00517822 | 0.0506191 | upstream-variant-2KB, intron-variant | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83709142 | CTTTTTAGCAGAGCT[C/G]TATGGAATCTGGGTC | 29979 |
rs116134165 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83693586 | AGAAGTTAGAAAACC[A/G]TATCAAATAAGAGTA | 29979 |
rs116332683 | snp | C/T | 0.0376037 | 0.131863 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83704787 | GCCGACACCATGCCA[C/T]TGCACTCCAGCCTGG | 29979 |
rs116441755 | snp | A/C | 0.0185938 | 0.0946107 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83679677 | GATTTCTCTCTTTAG[A/C]TTAACCATACATACA | 29979 |
rs116718665 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83693838 | TTTGCTACATACTAG[C/T]TGTGTGACCTGGAGG | 29979 |
rs117000243 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83699448 | CCTGGGCTCAACCTT[G/T]CTGGACTAGCTGGGA | 29979 |
rs117183060 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83670071 | TGCCAAGGGCTACAG[A/C]TGAATTTATGTGAAT | 29979 |
rs117273398 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83682462 | CTAGCCTCCGTGACT[A/G]AGCAAGATCCTGCCT | 29979 |
rs117360718 | snp | G/T | 0.00795532 | 0.062565 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83679411 | GTTGCAATTTTGTAT[G/T]CAACATATAAGGCAG | 29979 |
rs117399917 | snp | G/T | 0.0275645 | 0.114116 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83697727 | CACGCGGCTATTTTT[G/T]GTACCCTTTTTTTTT | 29979 |
rs117431201 | snp | C/G | 0.0295035 | 0.117819 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83704497 | CTACCATCAGAAAAG[C/G]CTACTTCAGAAAGAC | 29979 |
rs117559521 | snp | A/C | 0.0275645 | 0.114116 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83703776 | AAGCTTTATTAGTAA[A/C]CTTGAACAAGTAACA | 29979 |
rs117608988 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83670476 | ACACACATTTTTTGG[C/T]TTCCCAGCGCATACA | 29979 |
rs117667728 | snp | C/T | 0.00795532 | 0.062565 | intron-variant, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83706214 | ATCTACTGATACGTG[C/T]AACTTACTCTGAATT | 29979 |
rs117760699 | snp | C/T | 0.0287284 | 0.116357 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83674517 | AAGTTTCCAAGTGGC[C/T]TGTTAGCCAAAGGAA | 29979 |
rs117970453 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83708968 | GGCTTTTAAAGATGA[C/T]TTGCAAGGAATGTAC | 29979 |
rs117988241 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83686733 | CAATCTCATATTCTT[G/T]GCCTAGCGGTGGAGT | 29979 |
rs118159353 | snp | C/G | 0.0252325 | 0.109451 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83675534 | CAGATTTACTTTTGA[C/G]CTCATACCACCAGCA | 29979 |
rs137874862 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83693577 | ATAATTAAGAGAAGT[C/T]AGAAAACCGTATCAA | 29979 |
rs137966338 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83664759 | TAACAACAACAAATT[A/G]TATATATAAATTAGC | 29979 |
rs137967361 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83690247 | AGTCATTTGATAGAT[C/T]ACCCCCAATGACAAC | 29979 |
rs138041493 | snp | A/G | 0.00021418 | 0.0103462 | synonymous-codon | UBQLN1 | GRCh38.p7 | 9:83677830 | GGCAGTGCCGCTGGA[A/G]GCTGATGAACTCTGG | 29979 |
rs138094230 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83698458 | ATATTTTATAGTCTT[C/T]ATATCAATTGCACCT | 29979 |
rs138137643 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83676493 | AACCCTCTCAAAAGA[C/T]TGTTAGTATCAAAGT | 29979 |
rs138157005 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83665685 | CATCATTACAATAGA[A/T]CAAGGACACCAACCT | 29979 |
rs138238324 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83694574 | CATAAAACTGTACAC[A/T]GCCACAAATGTTAGT | 29979 |
rs138383470 | snp | A/G | 0.192715 | 0.243348 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83691046 | GGGAGGCTAAGGCAC[A/G]AGAATCACTTGAACC | 29979 |
rs138447638 | snp | A/C/G | 0.216028 | 0.255533 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83684806 | CAAGAGTGAAATTCC[A/C/G]TCTCAAAAAAAAAAA | 29979 |
rs138588326 | in-del | -/A | 0.0700422 | 0.173537 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83703525 | AATATTCCAAAATCC[-/A]AAAAAAAAAGAAAAT | 29979 |
rs138593223 | in-del | -/AAAAC | 0.477937 | 0.102688 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83677565 | AAGCTCTATCTCAAA[-/AAAAC]AAAACAAAACAAAAC | 29979 |
rs138594169 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83677127 | GCCCTGACCTCAAGA[C/T]GGGTGCTTGACAATC | 29979 |
rs138596239 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83694265 | TAGCAAGGATTCTCT[A/G]AATAGTTATCTGAAT | 29979 |
rs138812787 | snp | A/G | 0.00134471 | 0.0258949 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83665196 | TTAAAATCAGTGAAC[A/G]TAAATTTTTAAATCT | 29979 |
rs138824015 | snp | A/C/T | 0.00119737 | 0.0244387 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83672275 | CTGGAGTAGCACTTA[A/C/T]AATTTTCTTCAAGAA | 29979 |
rs138874171 | in-del | -/ACAAA/CAAAA | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83677589 | CAAAACAAAACAAAA[-/ACAAA/CAAAA]GCAACATGAAAAATA | 29979 |
rs138983349 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83683911 | CTGTAATCACAGGTA[C/T]TCAGGAGGCTGAGGC | 29979 |
rs139275400 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83682084 | ATTCAGGAGATCTAG[A/C]CCATCCTGGCTAATA | 29979 |
rs139315739 | snp | A/G | 0.00225733 | 0.0335197 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83686204 | TGTTTGCACAGCACC[A/G]TACAGTCTAGTTTCT | 29979 |
rs139421247 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83709252 | CAAGGCCTTCTGCTT[A/C]ATGAAGGATGACTAC | 29979 |
rs139428968 | in-del | -/CAAA | 0.00199481 | 0.0315187 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83675285 | CAACCCTCCAACAAC[-/CAAA]CATTGAATTACTATA | 29979 |
rs139463011 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83701694 | GAGAATGTGGTTATC[A/G]GAATCCTCATGCATT | 29979 |
rs139473303 | in-del | -/TGTATG | 0.0275645 | 0.114116 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83662243 | ACATGCAGAAAAACC[-/TGTATG]TGTGTGTGTATATAC | 29979 |
rs139495847 | snp | C/T | 8.23608e-05 | 0.00641667 | synonymous-codon | UBQLN1 | GRCh38.p7 | 9:83678525 | CCCTGGGATGCTTTC[C/T]AGGTTGCTCAAAGCT | 29979 |
rs139668587 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83666860 | TAGAAACCTCAACAC[A/G]CAAGTGGCAGGCACA | 29979 |
rs139706742 | snp | G/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83670316 | ACTTATCTTTCTAGT[G/T]TATTATAATTCTGTT | 29979 |
rs139815816 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83691383 | TTAAAACCTGATATC[C/T]AAAACAGCTGTAATC | 29979 |
rs139837541 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83687265 | TTTCCAGGGACCAGA[C/T]ACATAAAACCAGACA | 29979 |
rs139859586 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83673104 | GTGTGGTGGTACACA[C/T]CTGTAATCCCAGCTA | 29979 |
rs139889249 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83680666 | ACCCATACCTTGTGC[C/T]CTAATAATTATCTTC | 29979 |
rs140097122 | snp | C/T | 0.000371443 | 0.0136229 | missense, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83707571 | TCACGGTGACTTTCA[C/T]GATTTTGGGCTCCGC | 29979 |
rs140098034 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant, utr-variant-3-prime | UBQLN1 | GRCh38.p7 | 9:83667987 | ATTACAAAATTGCTA[C/T]GCATGTGCTTGTTAA | 29979 |
rs140100726 | snp | A/C/G | 0.00406476 | 0.0448988 | synonymous-codon, intron-variant | UBQLN1 | GRCh38.p7 | 9:83666356 | CTTACTCACTTGTTG[A/C/G]AGGAAAGTTGGGAGC | 29979 |
rs140114905 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83700517 | GGAATCACATAAATA[C/T]ACAATTTTTAGTTGT | 29979 |
rs140133107 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83706647 | ATACACTAAAATTAT[C/T]TGTTAAATTCCACCA | 29979 |
rs140140110 | in-del | -/AT | 0.498632 | 0.0261223 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83691199 | ATACACATATAATAC[-/AT]ATATATATATATGCC | 29979 |
rs140228622 | snp | C/T | 0.00358779 | 0.0422022 | utr-variant-3-prime | UBQLN1 | GRCh38.p7 | 9:83660171 | TAACCTTTGTACTTG[C/T]TTTCCTCCTGGGGAA | 29979 |
rs140268844 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83671199 | CTCCTCCATAGAAGT[C/G]TTGAACCCCTCAAAG | 29979 |
rs140299371 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83671598 | CTTTTCCTTAGCAAC[A/G]TCTCACCAGTAGACT | 29979 |
rs140306286 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83673397 | AAAAAACAAAGAAAT[C/T]AGCCAGGTGTGGTGG | 29979 |
rs140404937 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83675442 | CACAAGCAATGTCAA[A/G]GTGCTTTACAGACTT | 29979 |
rs140589064 | in-del | -/ATATGCTGACAATCT | 0.0283406 | 0.115616 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83676206 | CATAATACTGTACAA[-/ATATGCTGACAATCT]GATAGGCCAGCAGAG | 29979 |
rs140634829 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83688774 | GCTGAGGCAGGAGAA[C/T]TGCTTGAACCTGGGA | 29979 |
rs140791765 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83693585 | GAGAAGTTAGAAAAC[C/G]GTATCAAATAAGAGT | 29979 |
rs140802395 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | UBQLN1 | GRCh38.p7 | 9:83660064 | CCATTTGCCAGTACA[A/G]AAGTTTTTAAACCAA | 29979 |
rs140813548 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83674477 | CACAAAAAATAAAAA[C/T]GAAAATAAGACTGCA | 29979 |
rs140918210 | snp | A/T | 1.66125e-05 | 0.00288201 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83678437 | CTTGGAGCCAGTGGA[A/T]CACCTGCTCTTGTGC | 29979 |
rs141259181 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83702822 | TGACCCTAAGGCAAG[C/G/T]TGCCTTATCAAAGAA | 29979 |
rs141333195 | in-del | -/AAAC | 0.4087 | 0.193169 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83682487 | CTGCCTCTCTTAAAA[-/AAAC]CAAACAAACAAACAA | 29979 |
rs141415951 | in-del | -/TGAA | 0.0275645 | 0.114116 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83700392 | ATAAGTAGTTATTAC[-/TGAA]TATGTATTATTGTAC | 29979 |
rs141475396 | in-del | -/AC | 0.492037 | 0.0625946 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83662268 | TGTGTATATACATAT[-/AC]ATATACACACACACA | 29979 |
rs141488845 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83689773 | CCTTAAAGAGACAAT[A/C/T]TGCAACACAACCAGC | 29979 |
rs141606585 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83680413 | TGAAGTGACTTAGGC[C/T]CCTGGAAAGCCTCAG | 29979 |
rs141642061 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83678837 | ATTCTCCTGCCTCAG[C/T]CTCCCGAGTAGCTGG | 29979 |
rs141696561 | in-del | -/CAGTTTTG | 0.0185938 | 0.0946107 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83699139 | AACGGTCCAGGGTTT[-/CAGTTTTG]CAAGATGAGTTCTGG | 29979 |
rs141711599 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83686471 | CAGTATCTTGATGTT[A/G/T]GTAAGAAATGATTAT | 29979 |
rs141785166 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83669705 | AATTAATTAGAATCA[C/T]ATTCGGCACTTAATA | 29979 |
rs141807690 | snp | C/G | 1.64944e-05 | 0.00287175 | missense, intron-variant | UBQLN1 | GRCh38.p7 | 9:83666428 | TAGGGGATTATTCAG[C/G]ATCATCTATGGGGCA | 29979 |
rs141888683 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83672801 | CTGCAAACCTTCAAA[C/T]TGTGAAAATCACACT | 29979 |
rs141917237 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83672496 | TCAATGTTGTGTCTC[A/T]GAGAATAGGGAGACC | 29979 |
rs142002440 | in-del | -/A | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83688862 | TCAAAAAAAAAAAAA[-/A]GACATGCATCTATTC | 29979 |
rs142060877 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83709713 | CTATAAGGTAATAAG[A/G]TTTACCTGTAAGAAG | 29979 |
rs142060942 | snp | G/T | 0.0182019 | 0.0936463 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83664779 | TATAAATTAGCTAGG[G/T]GTGGTGGTGCACACC | 29979 |
rs142066874 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83670234 | GCCAAGTCAACTCAT[C/T]AGGTTTTTCATCTCC | 29979 |
rs142102641 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83668781 | CTGCCATTCTGAGCA[A/T]GACTATTATAATCTG | 29979 |
rs142131125 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83703813 | AATACCAAATGTATA[C/T]AGCACTGTAAAAAAT | 29979 |
rs142297216 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83682564 | TGGCTTCCCAGACCC[C/T]CTTCCATGTGTTCAG | 29979 |
rs142348719 | snp | C/G/T | 0.000677081 | 0.0183872 | missense | UBQLN1 | GRCh38.p7 | 9:83682956 | AGACACTTACCTAAA[C/G/T]CAAAAGGGTTGCTAG | 29979 |
rs142359394 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83695720 | AGGACATCAAACTAA[C/T]TCATAGTTGTATAAA | 29979 |
rs142409341 | in-del | -/TTTCTAC | 0.0551013 | 0.156571 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83689120 | ATAAGAAACCAGTAA[-/TTTCTAC]TTTCTGTTTCCATAC | 29979 |
rs142449377 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83671056 | CTGCTGCCTGCAATT[A/C]CTAGGCTCAAGGGAT | 29979 |
rs142500648 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83683587 | CAAAATATGCTGCAA[C/T]TGCCCCTCCTCTTTG | 29979 |
rs142538970 | snp | C/G/T | 0.00716904 | 0.0595202 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83687893 | ACTTCAGTAAATATT[C/G/T]TGAAGCTTTTCCATC | 29979 |
rs142553322 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83674359 | CAACATATATAAGCA[A/C]TGCCGGACCAACCAC | 29979 |
rs142633586 | snp | A/C/G | 3.29817e-05 | 0.00406078 | missense | UBQLN1 | GRCh38.p7 | 9:83677915 | GGTTGACTACCTTCA[A/C/G]CAGAGGATGTATTGC | 29979 |
rs142669512 | snp | C/T | 0.000153988 | 0.00877328 | missense | UBQLN1 | GRCh38.p7 | 9:83661872 | TGCAAGTTTGCTTCA[C/T]GGTTCAAAAATCCCA | 29979 |
rs142797913 | snp | C/T | 1.64743e-05 | 0.00287 | missense | UBQLN1 | GRCh38.p7 | 9:83678572 | TCATCTCCTGCATCA[C/T]TGCTGGATTCCTGGC | 29979 |
rs142838159 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83699714 | TTTTGATGAACAAGA[C/T]ATATTAACAGGAAGC | 29979 |
rs142874805 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83706113 | ATGCATTTCACTGCT[G/T]CCAAAATTACGTCAA | 29979 |
rs142882287 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | UBQLN1 | GRCh38.p7 | 9:83661529 | ATCTGGTCACCCAAC[C/T]ATAAAAGGTGATGTT | 29979 |
rs142883999 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | UBQLN1 | GRCh38.p7 | 9:83661180 | TGCTGTAAGATTCTA[C/T]ACAATTAGGAAATAC | 29979 |
rs142964672 | snp | A/G | 0.0279526 | 0.114869 | upstream-variant-2KB, intron-variant | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83708726 | CGATGACAGCTGTGC[A/G]CGAGCGCCCCCAGAT | 29979 |
rs142980085 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83692168 | TACCGTGCCAGATAT[A/G]GTACACTTTTCCGAA | 29979 |
rs142984848 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83666874 | CACAAGTGGCAGGCA[C/G]AGAGAAAATCTAGAT | 29979 |
rs143187337 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83703821 | ATGTATATAGCACTG[C/T]AAAAAATTAAGGCAA | 29979 |
rs143275539 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83676911 | TGTAGTATCTGAATA[C/G]CTGAAAGGAAGACAT | 29979 |
rs143429279 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83677550 | CTGTGCAACAAGAGC[A/G]AAGCTCTATCTCAAA | 29979 |
rs143498341 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83674772 | TGTATGGGGAGTCAA[C/T]GGTAAGTCTGAAGTG | 29979 |
rs143503799 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83664591 | AACCGATCTCTTAAT[A/T]AATAAATAAGTAAAT | 29979 |
rs143588139 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | UBQLN1 | GRCh38.p7 | 9:83660319 | TTCATTTTAGGTTAC[C/T]TTAACATTTTAATTT | 29979 |
rs143607698 | snp | A/C/G | 0.000265144 | 0.0115111 | synonymous-codon | UBQLN1 | GRCh38.p7 | 9:83669239 | CATGCTTCTCATGTA[A/C/G]GGGGCAGACAACATG | 29979 |
rs143683244 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83666782 | TTCATGAAGATATAT[G/T]TTCTACTACACTGGC | 29979 |
rs143717709 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83694831 | CCTCCAAACAATGTA[A/C]TGAAGCAGGTATTAC | 29979 |
rs143751282 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83662699 | GAGTACCTACCAAGA[A/G]CCAGAAACTATGCTA | 29979 |
rs143755407 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83698630 | ATACACAGTAAATTC[C/T]GGCTGGGTGCGGTGG | 29979 |
rs143843890 | in-del | -/TA | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83682291 | TCTCAAAAAATATAT[-/TA]ATATATATATTCCAC | 29979 |
rs143878718 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83696511 | GGGCAAGGTGGTGCA[C/T]GCCTGCAGTCCCAGT | 29979 |
rs143916731 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83700939 | TCAGAGATCACTCTT[A/G]GAATGGCTGGTGGGA | 29979 |
rs143923981 | snp | C/T | 0.0287284 | 0.116357 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83677523 | GCTGAGATCGTGCCA[C/T]TGTACTCCAGCCTGT | 29979 |
rs144073234 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83690793 | GTCGAAACACAGCCA[G/T]CTCTCCTTAGTATTT | 29979 |
rs144084317 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83677331 | AATTTGGGAGGCCAA[C/G]GCAGGCGGATCACCT | 29979 |
rs144151099 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83673677 | AAATTCAAATTTCAA[C/T]GCCCATGAATACCAT | 29979 |
rs144158928 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83682130 | TCTACTAAAAATACA[A/G]AAAAATTAGCCGGGC | 29979 |
rs144266055 | snp | C/T | 0.000510603 | 0.01597 | missense | UBQLN1 | GRCh38.p7 | 9:83663943 | GTCCAGGTTCAGTGG[C/T]TCCTGCTGTGGGACT | 29979 |
rs144280759 | snp | C/T | 8.23621e-05 | 0.00641672 | missense | UBQLN1 | GRCh38.p7 | 9:83679931 | CATGATCTGGACCAT[C/T]ATTTCAGGGTTAGAC | 29979 |
rs144287299 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83666027 | AAACCATAAAGCGTA[A/G]CATGACACAAGGAAG | 29979 |
rs144321778 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83671263 | ACTCCTGTTCATGTT[A/G]ATATTTTGACATCCT | 29979 |
rs144337732 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83670465 | TAAAGCAAGTCACAC[A/T]CATTTTTTGGTTTCC | 29979 |
rs144373682 | snp | C/G | 0.00953873 | 0.0683987 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83679682 | CTCTCTTTAGCTTAA[C/G]CATACATACAGGACA | 29979 |
rs144452583 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83695963 | TTTTTTTTTTTGAGT[C/T]GGAGTCTCACTCTGT | 29979 |
rs144596442 | in-del | -/T | 0.081446 | 0.184634 | intron-variant, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83706948 | GTTTCTACGTCATAA[-/T]TTTTTTTTTAAAGGT | 29979 |
rs144629014 | snp | G/T | 0.00119737 | 0.0244387 | utr-variant-3-prime | UBQLN1 | GRCh38.p7 | 9:83660067 | TTTGCCAGTACAGAA[G/T]TTTTTAAACCAAACT | 29979 |
rs144677877 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83699195 | ATTGTACAACAATGT[C/G]AATGTACTTAATGTC | 29979 |
rs144697323 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | UBQLN1 | GRCh38.p7 | 9:83661415 | CCACAAATTATAGAG[C/T]GCAAATGATTTGCTT | 29979 |
rs144783332 | snp | C/G | 0.00398564 | 0.0444627 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83708042 | CCGAGTCATCCCCGG[C/G]TGGCGCGACTTTGAG | 29979 |
rs144859352 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83672261 | CATTCATGTCTTCAC[C/T]GGAGTAGCACTTATA | 29979 |
rs144958976 | in-del | -/CTGT | 0.0528381 | 0.153711 | upstream-variant-2KB, intron-variant | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83709489 | TCCCCTTGCCTTCAC[-/CTGT]CTAACTTCTACTCAT | 29979 |
rs144994449 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83671878 | CTAGATGATATCTTC[C/T]TCCAATAGAAGGCTG | 29979 |
rs145031174 | in-del | -/AAAAACA | 0.173965 | 0.238157 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83666120 | TAGGTCCTCAAAAGC[-/AAAAACA]AAAATGTTCTTTCCT | 29979 |
rs145049267 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83682433 | CAGTGAGCTATGGAT[A/G]GCATCACTGCACTCT | 29979 |
rs145144160 | snp | A/G | 0.00199481 | 0.0315187 | upstream-variant-2KB, intron-variant | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83709550 | CACTCCCTACCATTT[A/G]GAGATATGGTTTTTC | 29979 |
rs145259475 | in-del | -/T/TT | 0.0700422 | 0.173537 | intron-variant, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83705935 | CTGTAACTTAGGGCA[-/T/TT]TAAAAAAAAAAAACT | 29979 |
rs145316357 | in-del | -/GAA | 0.02016 | 0.0983543 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83674238 | AGAACAAGAAAAAAG[-/GAA]GAAGGAGAGTTACAA | 29979 |
rs145324298 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83691349 | GATGATCCATTAACA[C/T]CGTATGTGGCAGAGA | 29979 |
rs145454717 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83702128 | GACAAAAAATAGATC[A/G]GTAGTTGCCTAAGGC | 29979 |
rs145461084 | snp | A/G | 0 | 0 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83687278 | GACACATAAAACCAG[A/G]CAAGAGAAAAGAGCA | 29979 |
rs145473718 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83663404 | TTTACGAGATATATA[C/T]ATATGTAACACAAGC | 29979 |
rs145491972 | in-del | -/T | 0.00517822 | 0.0506191 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83674499 | AGACTGCAACCAAAG[-/T]TTAAGTTTCCAAGTG | 29979 |
rs145557811 | snp | A/G/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83710064 | ACAAAAACAGACATA[A/G/T]GATCTGATTTGGCCT | 29979 |
rs145661694 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83676177 | TGCATCAAATGTCAC[A/C]GTTGAGTAAGAATCA | 29979 |
rs145697046 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83672506 | GTCTCAGAGAATAGG[A/G]AGACCCAAGAAGAGG | 29979 |
rs145826278 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83691920 | ACAGACAACTGCATA[G/T]GACTACCATTCATAA | 29979 |
rs145844229 | in-del | -/ATCT | 0.0810805 | 0.184299 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83687793 | ACTGATTTTTAAAAA[-/ATCT]GTTTTACCTTTGTCA | 29979 |
rs145849587 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83668863 | GCTTTCAAGATTTAC[A/G]TTTCATTAAGTAGTT | 29979 |
rs145856007 | snp | C/T | 0.001027 | 0.0226373 | synonymous-codon | UBQLN1 | GRCh38.p7 | 9:83669284 | TGGGTTTTCAGTTAT[C/T]TGTTGCAACAAGCTC | 29979 |
rs146037406 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83664852 | TGAGCCCGAGAGGTC[A/G]AGGCTGCAGTGAGCC | 29979 |
rs146037689 | snp | C/G | 0.000115933 | 0.0076127 | missense | UBQLN1 | GRCh38.p7 | 9:83678446 | AGTGGATCACCTGCT[C/G]TTGTGCAGCACTCAG | 29979 |
rs146081089 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83706454 | GTTACACACCTCACT[A/G]CTTCACAAAATACAC | 29979 |
rs146091499 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83698694 | CCAAGGGGGCAGATC[A/G]CTTGAGCTCAGGAGT | 29979 |
rs146131444 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83699900 | AAGGCACCCATTATA[A/T]GCAATGGCTCTTAAA | 29979 |
rs146245145 | in-del | -/A | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83689051 | CATTTTCATTACCTC[-/A]AAAAAATCTATACCC | 29979 |
rs146251461 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83682077 | ATCACAAATTCAGGA[C/G]ATCTAGACCATCCTG | 29979 |
rs146291236 | snp | A/C/T | 3.30181e-05 | 0.00406303 | missense | UBQLN1 | GRCh38.p7 | 9:83663882 | ACTGATACCTGAGGA[A/C/T]TTACTCCAGCAAGAG | 29979 |
rs146323320 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83670274 | TTCCATCCAGTTATA[C/T]CAGGCTTAAGACATC | 29979 |
rs146373975 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83666829 | TCAATACATGAACTA[C/T]GTAACATGGCTTGCT | 29979 |
rs146618126 | in-del | -/AG | 0.00636936 | 0.0560724 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83675324 | TCGTTTTTGTTAGAG[-/AG]TTGGTAATGCTTATG | 29979 |
rs146622667 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83692522 | TAGCTCACTGACACT[A/G]TTCCTCTGCAGAAAA | 29979 |
rs146724128 | snp | A/C | 0.0104278 | 0.0714503 | missense | UBQLN1 | GRCh38.p7 | 9:83677768 | GCAGTAGTACTCTGC[A/C]CAGAAGTGCCACTGG | 29979 |
rs146742366 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83675089 | CAATGAGGAGCACTG[C/T]TAACTCCTGTAAACT | 29979 |
rs146845435 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83662797 | GCTTGAAAACAGAAA[C/G]CAGGCCAGGCTCACG | 29979 |
rs146866128 | snp | G/T | 0.00478085 | 0.0486577 | downstream-variant-500B | UBQLN1 | GRCh38.p7 | 9:83659788 | CACCTACCTTCCCAG[G/T]GTGCTATCTTTTTAT | 29979 |
rs146993231 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83697689 | GCTTCCCAAGTAGCT[A/G]GGACTACAGGCATGC | 29979 |
rs147220367 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | UBQLN1 | GRCh38.p7 | 9:83660549 | TTAAAACGGCTCTTT[A/G]TTTTTCACCCCTGAA | 29979 |
rs147243490 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83691351 | TGATCCATTAACATC[A/G]TATGTGGCAGAGACA | 29979 |
rs147253463 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83694872 | AAAAATGTAGCCAGT[A/G]AGGCTGAGATGATTA | 29979 |
rs147360662 | snp | C/T | 0.0287284 | 0.116357 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83677380 | CCAGCCTGACCAAGA[C/T]GGAGAAACCCTGTCT | 29979 |
rs147369910 | snp | A/G | | | synonymous-codon | UBQLN1 | GRCh38.p7 | 9:83677848 | TGATGAACTCTGGGA[A/G]GTCTGTGGAGCCCAT | 29979 |
rs147421462 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83691031 | CAATCCCAGCTACTC[A/G]GGAGGCTAAGGCACG | 29979 |
rs147431416 | snp | C/G/T | 0.00517822 | 0.0506191 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83694536 | ACTGAATATGTAACA[C/G/T]GTATGAGAAAGGGGC | 29979 |
rs147527655 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83673257 | ACCAAAACAATTTTT[A/G]GTCGGGTGCAGTGAC | 29979 |
rs147536809 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83677075 | TGGGAATCTGATTTT[C/T]AATAAACCTGGCAGG | 29979 |
rs147560206 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83668758 | CTTTAATAAATGCTA[C/T]TTTACAACTGCCATT | 29979 |
rs147570190 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83671124 | GTATGAGCCAACACA[A/C]CTGGCAGGCTCCACT | 29979 |
rs147576408 | snp | A/G | 0.00279162 | 0.0372561 | upstream-variant-2KB, intron-variant | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83709657 | ACTTTGCAATTATCT[A/G]TGTCTACATTATTGT | 29979 |
rs147619806 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83703078 | CTCACATATATAACT[A/C]TCCATTCTTCTAGAT | 29979 |
rs147682329 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83687516 | ATCTCAACAGATAAG[A/G]AAATTGCTGCCAAGA | 29979 |
rs147770620 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83673710 | TATTGGAACAGTCAT[C/T]CTCACTTATTGTCTA | 29979 |
rs147786783 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83671522 | TCTCCTTGCACATCT[C/T]CATCAAAGCTCTTGG | 29979 |
rs147830057 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83669067 | GAGACACAGTTTACT[C/T]ATTTTTCTAGTGTAT | 29979 |
rs147884186 | snp | A/C | 0.0115144 | 0.0749975 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83686944 | AAAAAAATCTGAAAT[A/C]TGAGACACTTCTGGT | 29979 |
rs148048017 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83669692 | CAAGACTGCAAAGAA[C/T]TAATTAGAATCATAT | 29979 |
rs148126802 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83672694 | AAAAAGCCTGAAATA[C/T]TGTGAGAATTATCAA | 29979 |
rs148190428 | snp | A/C | 0.0166325 | 0.0896639 | utr-variant-3-prime | UBQLN1 | GRCh38.p7 | 9:83660144 | CAATCTCTTCTACTT[A/C]TGCCTCCACCGTAAC | 29979 |
rs148231237 | snp | C/T | 1.6522e-05 | 0.00287414 | missense | UBQLN1 | GRCh38.p7 | 9:83677762 | TTTGGCGCAGTAGTA[C/T]TCTGCCCAGAAGTGC | 29979 |
rs148245385 | in-del | -/T | 0.0275645 | 0.114116 | utr-variant-3-prime | UBQLN1 | GRCh38.p7 | 9:83660116 | GCAAAGACACATGAA[-/T]TACCCTTCTTAACAA | 29979 |
rs148285450 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83704426 | GGTGATAAGCGTCAA[C/T]TTTTATCACATTTTC | 29979 |
rs148355197 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83676963 | GTGGACAAAAGTAAA[C/T]TTCTAACCTGTTCAC | 29979 |
rs148439740 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83673864 | TGGAGTGCGGTGATG[C/T]CATCACAGCTCACTG | 29979 |
rs148502447 | snp | G/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | UBQLN1 | GRCh38.p7 | 9:83661503 | AATAAACTGGACAGA[G/T]GCAGGACAAAATCTG | 29979 |
rs148595828 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83708456 | AAATAGCGGCGAGGT[A/G]TTTTGTTATTTTAAT | 29979 |
rs148658630 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83690898 | ATCCCAACACTTTGG[A/G]AGGCCAAGGCGGGTG | 29979 |
rs148717761 | snp | C/T | 0.0279526 | 0.114869 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83682549 | AGTTTTAGGCGAGGC[C/T]GGCTTCCCAGACCCC | 29979 |
rs148755587 | snp | C/T | 3.29468e-05 | 0.00405861 | synonymous-codon | UBQLN1 | GRCh38.p7 | 9:83679973 | CTGCATCTGACTCTG[C/T]AGTTCAGAGAAGTTG | 29979 |
rs148815581 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83664173 | GCCTGGTGCAGTGGC[A/T]CATTCTGGGAGACCG | 29979 |
rs148867484 | snp | A/G | 0.00153106 | 0.0276258 | synonymous-codon | UBQLN1 | GRCh38.p7 | 9:83669197 | CACCTGTGCAGCAAG[A/G]TCAGGATTCTGGCTT | 29979 |
rs148972185 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83691984 | GTCACCTAATTTAGA[C/T]ACTAGAACCACTTCC | 29979 |
rs149023278 | snp | A/G | 0.141596 | 0.225274 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83697380 | ACATAATGAAACCCC[A/G]TCTCTACTAAAAATA | 29979 |
rs149120187 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83672031 | TACATTATGGAGTTG[A/G]CTTCTTTCCTTAAAC | 29979 |
rs149127525 | in-del | -/G | 0.00755907 | 0.0610114 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83700309 | GGGAACAGCTTAAGA[-/G]GAAGCTTCCACAAAA | 29979 |
rs149280816 | in-del | -/ACTC | 0.0178098 | 0.0926698 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83703700 | GTAAAAATTTATGTT[-/ACTC]AGTTGATTCTGAGTG | 29979 |
rs149286302 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83694362 | TTAGCTCCTTACTCA[A/G]TATTGCTAATAGTAT | 29979 |
rs149428874 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83684640 | AACATGAGGAAACCC[C/T]GTCTCTATCAAAAAT | 29979 |
rs149437085 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83673132 | CTACTGGGGAGGCTG[A/G]GAAGGGAGAATCGTT | 29979 |
rs149481293 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83690397 | GGGACAAAATCCATG[C/G]TGCCCAAAGTGAGAA | 29979 |
rs149551631 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83665929 | TGAGATCTACCCCTT[A/G]GGGAAAAAAAGCCTT | 29979 |
rs149603095 | in-del | -/AG | | | upstream-variant-2KB, intron-variant | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83709160 | TGGAATCTGGGTCTA[-/AG]AGAATCCTGAGGGTA | 29979 |
rs149603256 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83670363 | TTTCCTATTTTCTCA[C/T]GTTGTAAATTTTAAC | 29979 |
rs149674693 | in-del | -/TAC | | | intron-variant, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83705867 | GAAAAATACACACAG[-/TAC]TACTATAGGCTCTAT | 29979 |
rs149741121 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83686942 | AAAAAAAAATCTGAA[A/C]TCTGAGACACTTCTG | 29979 |
rs149835068 | snp | C/T | 0.000510814 | 0.0159733 | synonymous-codon | UBQLN1 | GRCh38.p7 | 9:83665086 | ACCCTGCTGAATCTG[C/T]AACAAGGCCTGCATT | 29979 |
rs149891395 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | UBQLN1 | GRCh38.p7 | 9:83668145 | ATCTTCCATAAAATG[C/T]ACCTCCAATATACAG | 29979 |
rs149910049 | snp | A/G | 0.030665 | 0.119967 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83677517 | CGGTGAGCTGAGATC[A/G]TGCCATTGTACTCCA | 29979 |
rs150057006 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83663296 | CAGGTTTAAACTGGC[A/G]ATCATCTTTATATAA | 29979 |
rs150069194 | in-del | -/TCTC | 0.0023933 | 0.0345097 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83694619 | ATTTATTTTTTAGAT[-/TCTC]TCTAATTTAAATCTG | 29979 |
rs150106876 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83694063 | ACTTTAAAAGCAACA[C/T]TGTCACCCTTTACAA | 29979 |
rs150151550 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83709992 | ATCACAGAGTAATCA[C/T]AGACAATACATACAT | 29979 |
rs150202978 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83669932 | GTGATCTTGGGCAAG[A/T]TATCTAGCGTCTTCA | 29979 |
rs150272999 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83683602 | TTGCCCCTCCTCTTT[A/G]AGTATAATGTACACA | 29979 |
rs150316848 | snp | C/G | 0.00993419 | 0.0697739 | utr-variant-3-prime | UBQLN1 | GRCh38.p7 | 9:83660178 | TGTACTTGTTTTCCT[C/G]CTGGGGAAAGTGTCA | 29979 |
rs150337807 | snp | A/C/G | 0.000164869 | 0.00907803 | missense | UBQLN1 | GRCh38.p7 | 9:83677795 | CTGGCAGTACTACCA[A/C/G]TAGTGCCACCCACAG | 29979 |
rs150362158 | snp | C/G | 0.0119091 | 0.0762411 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83671849 | GAATTCACTTCTCTC[C/G]AGAAATGAAAATTCT | 29979 |
rs150411464 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83705037 | CCAGGATGGTGGAGG[C/T]ATGAATTAGGAATCC | 29979 |
rs150475499 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83688974 | GTAATTCACTCATTT[A/G]AAGTATACGATTCAA | 29979 |
rs150509304 | snp | A/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83680529 | GGAGATAGAGCTCTA[A/T]GCAAATTCTTCAACA | 29979 |
rs150561321 | snp | G/T | 0.0482946 | 0.147699 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83686562 | GCTAAGGCCTAACAA[G/T]GCATTGCTTCCCAAT | 29979 |
rs150632104 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83662162 | TGTCAAATAGATCAC[C/G]ACTCTACTTTAGGGG | 29979 |
rs150676084 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83672847 | CAAAATGAGGTATAT[C/G]TGTATTCTAAGATAG | 29979 |
rs150790486 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83665569 | TACCAGTAAGGTACA[C/T]TCTAAAACAACAGTT | 29979 |
rs150867100 | snp | C/T | 8.04861e-05 | 0.00634323 | missense | UBQLN1 | GRCh38.p7 | 9:83686133 | GTATGTGATTTAAAA[C/T]GTTTAGAGATTTCTT | 29979 |
rs150990424 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83674409 | TCACAGAAAAGCAAT[A/C/G]GTCAGAAGAAATATA | 29979 |
rs151042416 | snp | A/G | 0.0256215 | 0.110247 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83678301 | GCTGGGATTACAGGC[A/G]TGAGCCACTGCACCC | 29979 |
rs151070080 | snp | C/G | 0.000312992 | 0.0125059 | missense | UBQLN1 | GRCh38.p7 | 9:83663984 | CTAGGTGTGGCGTTA[C/G]ATCCATTAGTTCCCG | 29979 |
rs151106399 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | UBQLN1 | GRCh38.p7 | 9:83667888 | TCTGTAATAAAAGAC[A/G]TGCCAATCTAGTACT | 29979 |
rs151149527 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83709147 | TAGCAGAGCTCTATG[A/G]AATCTGGGTCTAAGA | 29979 |
rs151296824 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83688679 | CATCTTGGCCAACAT[C/G]GTGAAACCCCGTCTC | 29979 |
rs151314851 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83701569 | CAGTTTTCCTCAGAG[G/T]GCCCCCAGCAAAAAT | 29979 |
rs180717820 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83662622 | CTTGTAAGTTAACTT[A/C]TGTCACAATTAATTC | 29979 |
rs180823134 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83681872 | CCAAATGGTAGAGCT[A/G]TAATACAGCAGAATG | 29979 |
rs180856367 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83701149 | TTGTTTAGGTTATAG[C/T]TGTTGATATTTATAA | 29979 |
rs180965294 | snp | A/C/T | 3.34198e-05 | 0.00408766 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83678639 | GAAAAAAAAAAGGCA[A/C/T]TGAAATACACATGAA | 29979 |
rs180981514 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant, downstream-variant-500B | UBQLN1 | GRCh38.p7 | 9:83667492 | ATACAATAACAAAAG[C/T]AGATGTCAGACAACC | 29979 |
rs181263779 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83700071 | ACAAACCACTCACTA[C/T]GTAATGAATTAACTT | 29979 |
rs181265367 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83681704 | AGATAGCAGTGCTCA[C/T]CAAACATTTCATTTT | 29979 |
rs181268164 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83673612 | ATTTTTAAATAGTTA[A/C]GGGAAAAAAAATCCA | 29979 |
rs181281090 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83691851 | GCACTTCATGCTAAA[A/G]GTTGGAAAACATGTT | 29979 |
rs181332455 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83662159 | TCATGTCAAATAGAT[C/T]ACGACTCTACTTTAG | 29979 |
rs181399380 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83678109 | TCACTGCAAGCTCCG[C/T]CTCCTGTGTTCACAC | 29979 |
rs181581253 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83705108 | CACACCCGCTAAAAT[A/G]GCTAAAATTACAGAG | 29979 |
rs181702248 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83688580 | ATTAAACACATGCAT[C/T]GGGCGGGGTGCAGTG | 29979 |
rs181706023 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83663014 | CCAGGAGGTGCAGGT[C/T]GCAGTGAGCTGTGAT | 29979 |
rs181712160 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83682613 | AATGCAGTCTGATCC[C/T]TTCCTTTTACAAATG | 29979 |
rs181713842 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83702232 | TAAAATTGACTACAC[A/G]ACCCTGTGAATGTAT | 29979 |
rs181782452 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83696468 | AAACAAAAAAATTTT[A/T]AAAAAAAACCCAATA | 29979 |
rs181787716 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | UBQLN1 | GRCh38.p7 | 9:83668387 | ACAGAAGCCATTTTT[A/G]ACGAACAGCAAATAT | 29979 |
rs181848666 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83672738 | GACATGAAGTGGGCA[C/T]ATGCTGTTGGAAAAA | 29979 |
rs181858531 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83709690 | AAAAATGTTTGATGT[A/G]TGTGACACTATAAGG | 29979 |
rs181978129 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | UBQLN1 | GRCh38.p7 | 9:83668050 | TATTAGCCAAATACA[C/T]ACTTAAAATGGCTTA | 29979 |
rs181990028 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83687630 | AAAAAATCTTGTGGG[G/T]ACAAGGAAGGGAAGG | 29979 |
rs181993985 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83704948 | CTATAACATCATATA[C/T]TGACTGAAAGGAATT | 29979 |
rs182099550 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83691337 | CAAAGGCTAAAAGAT[A/G]ATCCATTAACATCGT | 29979 |
rs182143012 | snp | C/T | 0.00120627 | 0.0245292 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83697783 | CTCTTATCCCACAGG[C/T]TGGAGTGCGATGGCA | 29979 |
rs182179163 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83674090 | AAGTATGAGCCACCA[G/T]GCCACACCTGGCCTC | 29979 |
rs182194705 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83692618 | AGCACTTTGGGAGGC[C/T]GAGGCAGGCGGATCA | 29979 |
rs182407118 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83679148 | GGCCAGTTTCCCCCC[C/T]AAAACCATAGTAAGC | 29979 |
rs182557486 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83698775 | CAAAGTAGCCAAGCA[C/T]GGTGATGTGAGCTTG | 29979 |
rs182560197 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83680368 | GTATCTTTTATTATT[C/T]ATTACAAGCCCTTTT | 29979 |
rs182569171 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83684008 | CCTGGGTGACAGAGA[C/G]AGACTCTTGAAAAAC | 29979 |
rs182702227 | snp | A/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83674847 | GGTAAGACCATTTTT[A/T]AAAAAGTTGAGAAAT | 29979 |
rs182703414 | snp | C/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83702444 | TTTCTCAGATATCTT[C/G]CTATACTGATTCAAT | 29979 |
rs182711860 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83694111 | CATCCAAACTTGCTT[G/T]TAAACAACCATTCTC | 29979 |
rs182717410 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83669035 | TACTGCAAAGAAACA[C/T]ACGGTCTAAAAAATT | 29979 |
rs182828816 | snp | A/C | 0.00953873 | 0.0683987 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83705372 | CCTCAGCCTCAGCCT[A/C]CCCAGTAGCTGGGAT | 29979 |
rs182848923 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83664844 | GAATCCCTTGAGCCC[A/G]AGAGGTCGAGGCTGC | 29979 |
rs183005194 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83664528 | AGGCTGAGGTGGGAG[A/G]ATCACCTGAGCTTAG | 29979 |
rs183022566 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83679695 | AACCATACATACAGG[A/G]CAATCTCATTAACCA | 29979 |
rs183038029 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83698213 | GGGAAGAAAGAGCCA[A/G]TGATATTTGAGGGTA | 29979 |
rs183124583 | snp | G/T | 0.000399281 | 0.0141238 | downstream-variant-500B | UBQLN1 | GRCh38.p7 | 9:83659555 | AATTTTAAGTATTTT[G/T]AACCCCTTAAGATGT | 29979 |
rs183127527 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83688845 | CAGCCTGGGCGATGA[C/G]AGCGAAACTCCGTTT | 29979 |
rs183139187 | snp | A/T | 0.02016 | 0.0983543 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83703695 | TGTAAGTAAAAATTT[A/T]TGTTACTCAGTTGAT | 29979 |
rs183247637 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83669845 | ACATTTAACATTTGA[A/C]ACCATAGAGCACAGT | 29979 |
rs183267367 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83689427 | ATGAATTAGTAAAAA[C/T]AGAAAAGCTATGAAC | 29979 |
rs183277708 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83706849 | ATACTAAAAGGGAAA[C/G]AGCAAGTCATCAGTG | 29979 |
rs183286747 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83683343 | CGTGAACCCAGGAGG[C/T]GGAGCTTGCAGTGAG | 29979 |
rs183334250 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83690051 | ATAAATCAGTACATT[C/T]TGGAATAACATTTTG | 29979 |
rs183573910 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83670398 | TTTTTTTTTCACATC[C/T]TAGAGTCCAACCTTG | 29979 |
rs183587500 | snp | C/T | 1.93086e-05 | 0.00310707 | missense, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83707538 | GCACGGCGAATTCCT[C/T]CTTTTCCTTCGGGGT | 29979 |
rs183699654 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83674549 | CCAAGTACTAGTGAT[C/G]ACTAATTTAACAGTT | 29979 |
rs183710808 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83675985 | TTTTGTCTCTTGATG[A/T]AATACATTCTCCATT | 29979 |
rs183711028 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83694455 | TGATGTTTAACCTTA[C/T]AGTAGTCTTATTTAA | 29979 |
rs183723891 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, utr-variant-3-prime | UBQLN1 | GRCh38.p7 | 9:83667853 | CAGATAACAAGAACA[C/T]TGTAAAAGTTTCTAA | 29979 |
rs183924512 | snp | A/C/G | 0.00119737 | 0.0244387 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83693149 | TCTTTCTCAACAACC[A/C/G]TAAGAATCAAAATTC | 29979 |
rs184050341 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83671489 | TGTGTTAGTTAACAG[A/G]CATAAAAACAACATT | 29979 |
rs184136792 | snp | A/C | 0.0256215 | 0.110247 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83678183 | CCCACCACCACGCCC[A/C]GCTAATTTTTTGTAT | 29979 |
rs184151209 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83696525 | ACGCCTGCAGTCCCA[C/G]TTTCTTCAGAAGCTG | 29979 |
rs184266196 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83687299 | GAAAAGAGCATCATG[C/T]TATAAAGAAACACTT | 29979 |
rs184270142 | snp | A/G | 0.000169414 | 0.00920208 | utr-variant-3-prime | UBQLN1 | GRCh38.p7 | 9:83661743 | TAAAGTTTAAGAGCC[A/G]TTATCAAAAATAAAT | 29979 |
rs184276565 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83681427 | ACAAGAAAATAAATG[C/T]CTATACAGATGCTAA | 29979 |
rs184279585 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83699825 | TGAAAGGAGCTATAG[A/G]TAACACATAAGCAAA | 29979 |
rs184421855 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83704662 | AAACCCTGTCTCTAC[C/T]ACAAATAGGAAAATT | 29979 |
rs184560403 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83681789 | CTACAAGAAATGATA[C/T]ATGCCACTTCTGGCC | 29979 |
rs184576464 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83665930 | GAGATCTACCCCTTG[A/G]GGAAAAAAAGCCTTC | 29979 |
rs184590351 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83684612 | AGTTCAGGAGTTCGT[A/G]ACCAGCCTGGCCAAC | 29979 |
rs184698912 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83700222 | TTCTAGAAGAGTAAT[A/G]TTCCAGGCAGAGAAG | 29979 |
rs184781395 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83662329 | AGATAGTTCAGAATT[A/C]GATGATTTGTGTAGC | 29979 |
rs184782720 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83690291 | CCACATATCATCACG[G/T]ATACCTCAACACGAG | 29979 |
rs184818930 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | UBQLN1 | GRCh38.p7 | 9:83667167 | AAACTTCAAATAAAC[A/G]TTAAGAATTTAAAAA | 29979 |
rs184938782 | snp | A/C | 0 | 0 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83703882 | GAAACCAATGGAAAA[A/C]TAGGAAAATAAATTA | 29979 |
rs185044180 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83685772 | CAAATAATTTAGGTA[C/T]AATAACTAAATACCA | 29979 |
rs185067214 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83672099 | TCTGCAGATTCCTTA[C/T]CTCTCAGCTTTCATA | 29979 |
rs185085560 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83691119 | CTCCAGCCTGGGTGA[C/G]AGAGAGGCACTCGTC | 29979 |
rs185090846 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83709108 | TGTTCTGAGAATAAA[A/T]ACTGTTACATAAACA | 29979 |
rs185134703 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83697484 | GTGAACCCAGGGGGC[A/G]GAGGTTGCAGTGAGC | 29979 |
rs185149755 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83669450 | TTATACATATTATGT[A/G]TCAACTGAACTACGA | 29979 |
rs185156852 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83688977 | ATTCACTCATTTAAA[A/G]TATACGATTCAATGG | 29979 |
rs185282629 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83673648 | AATATTTTGTGAAAC[A/G]TGAAAACTATATGAA | 29979 |
rs185295477 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83692241 | TGTTTTTATCTAAAT[A/G]GAATTTGTCCTACAG | 29979 |
rs185456924 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83677549 | CCTGTGCAACAAGAG[C/T]GAAGCTCTATCTCAA | 29979 |
rs185488943 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83695292 | CAACCTCCACCTCCC[A/G]GGTTCAAGTGATTCT | 29979 |
rs185584143 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | UBQLN1 | GRCh38.p7 | 9:83661307 | ATGTGCATACTCTAT[A/G]TTGTATACAAATAAA | 29979 |
rs185705896 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83699346 | ATGTGGCTCATACTG[C/T]TTTTTGTTTTTAAGA | 29979 |
rs185726946 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83681117 | GCAGAATTCACCTAT[A/C]AACACTGGGTACAAG | 29979 |
rs186143779 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83678907 | TTGTATTTTTTAGTA[A/G]AGACGGGGTTTCACC | 29979 |
rs186161716 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83702286 | TGGTGAACTGTATGG[C/T]AGGCAAATTACACTT | 29979 |
rs186166205 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83705709 | GCAAACAGCCCAGGT[A/G]ACCTTCAACAGTGAA | 29979 |
rs186286563 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime | UBQLN1 | GRCh38.p7 | 9:83668296 | TTTAGAAAATAAAAA[A/C]CATTCATTTGACTTA | 29979 |
rs186292156 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83687698 | GAAAATCAGAGATAG[A/G]TGCATGAAAGTTCCT | 29979 |
rs186298908 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83704979 | TTTCTATTTATAAAA[C/T]ACTGATTATTTCTAA | 29979 |
rs186376868 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83674457 | TCTCATCATAGCCAC[G/T]TTTTCACAAAAAATA | 29979 |
rs186381367 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83692886 | AATAATAAAAAAATA[C/T]TTTCATCTAGGGAAT | 29979 |
rs186471632 | snp | G/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83705202 | GCGGGATGGTAAAAT[G/T]ATACAAGCATTTTTC | 29979 |
rs186531183 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, synonymous-codon | UBQLN1 | GRCh38.p7 | 9:83668545 | CTAAGGATGAGGCCC[C/T]AACCATCGGTACTGT | 29979 |
rs186693988 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83691567 | GATGCAGTAGAGTAG[C/G]ACACTACACCACACA | 29979 |
rs186760084 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83688581 | TTAAACACATGCATC[A/G]GGCGGGGTGCAGTGG | 29979 |
rs186913405 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83673050 | GCCTGGCCAACATGG[C/T]GAAACCCCGTCTCCA | 29979 |
rs187003265 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83679190 | TGAGTCACTGTAACA[A/C]GAAAGAGTTCCCTCC | 29979 |
rs187119537 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83675042 | TACTCTGGAAAACAT[C/T]TGGATCTATCATGTT | 29979 |
rs187132008 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83694236 | TTCCCGCAGAATCAC[A/G]TATTAACAGCATTTA | 29979 |
rs187222378 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83697928 | TTTAGTAGAGACGGG[G/T]TTTCTCCATGTTGGT | 29979 |
rs187284337 | snp | C/G | 8.50261e-05 | 0.00651965 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83679735 | AAATAACAAATATAT[C/G]ATTTTTTAGCTAAAC | 29979 |
rs187287295 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83698315 | AAAGCTTTATTAGCT[C/G]TGCTAATTCAGCAGT | 29979 |
rs187365147 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83684690 | GTGGCGCATGCCTGT[A/G]ATTCCAGCTACTTGG | 29979 |
rs187393289 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83703761 | ATTGGAAAAAAGCTT[A/C]AGCTTTATTAGTAAC | 29979 |
rs187405719 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83662710 | AAGAGCCAGAAACTA[A/T]GCTACGCTAGCTTAT | 29979 |
rs187422221 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83701280 | TCTCAGTGATAAGAG[G/T]GGCATTATTTTAAAT | 29979 |
rs187452815 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83666234 | CGAATTGACAGCATT[A/T]TTGGTCTCTATTCTA | 29979 |
rs187569065 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83669891 | CAGGAGCCTGATTAC[A/G]TGGGTTCAAATCTAA | 29979 |
rs187599584 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83699068 | ATTCAGAGACAGAAA[A/G]AAGAATGGTGGTTGC | 29979 |
rs187660765 | snp | A/G | 0.00159617 | 0.0282053 | downstream-variant-500B | UBQLN1 | GRCh38.p7 | 9:83659611 | TAAATAAACATATTA[A/G]AAACAAAAACCATAC | 29979 |
rs187662832 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83682142 | ACAAAAAAATTAGCC[A/G]GGCGTAGTGGCACAC | 29979 |
rs187728321 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83689684 | ATGACCTAAGTGGGA[C/T]ACAAAAAGACCTAAC | 29979 |
rs187729238 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83707013 | AGAACTAAATATACA[C/T]ATGCACCTCACCCCA | 29979 |
rs187734173 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | UBQLN1 | GRCh38.p7 | 9:83661351 | TAGTATAAATCTTAC[A/G]GCATTGTTTGCAAAA | 29979 |
rs187832826 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83683798 | GAGGCCGAGGCAGGC[A/G]ATCAACTGAGGTCAG | 29979 |
rs187873813 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83684098 | AGGGTTATGAGCCAG[C/T]TTTACTCTGGCCCTT | 29979 |
rs187877959 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83665681 | CTTACATCATTACAA[C/T]AGATCAAGGACACCA | 29979 |
rs187965430 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83680408 | GCTAATGAAGTGACT[C/T]AGGCCCCTGGAAAGC | 29979 |
rs188094184 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83664587 | CAAAAACCGATCTCT[C/T]AATAAATAAATAAGT | 29979 |
rs188112490 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83670916 | CATCTGTACAAGTTT[C/T]TTCATGGCATTGTAG | 29979 |
rs188151586 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | UBQLN1 | GRCh38.p7 | 9:83667940 | AAAAAAATAGTATGT[C/G]AGTGCTCAAGTCACT | 29979 |
rs188157294 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83687316 | ATAAAGAAACACTTA[C/G]TTATACTATTCTCAG | 29979 |
rs188159355 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83704682 | ATAGGAAAATTAGCC[A/G]GGTGTGGTGTGGCAT | 29979 |
rs188213444 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83702602 | TAACTCACGATCTGC[A/G]AAATACTATTTCAAT | 29979 |
rs188288860 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83671734 | GCATAATTTTTAAGG[C/T]CCTAGGATTACTGGA | 29979 |
rs188299931 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83690502 | AAACACGAACCTGTA[C/T]ATTTATGACACATGT | 29979 |
rs188313102 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83708643 | AGCTTATTTACCGCC[C/T]TCGGGTTAGCCCGGT | 29979 |
rs188394702 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83690063 | ATTTTGGAATAACAT[C/T]TTGCAACAGAAGTTG | 29979 |
rs188458319 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83696620 | CTTCAGGTTGGGTGA[C/T]AGAACAAGATTCTGT | 29979 |
rs188468494 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83693443 | CTCTCAAGGTATCTT[C/G]TATCTGCCTTTTTCT | 29979 |
rs188539390 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83678219 | GTAGAGACGGGATTT[C/T]ACCGTATTAGCCAGG | 29979 |
rs188692079 | snp | A/G | | | missense | UBQLN1 | GRCh38.p7 | 9:83661873 | GCAAGTTTGCTTCAC[A/G]GTTCAAAAATCCCAT | 29979 |
rs188740719 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83681225 | CAAGGAGAAACCTAA[A/C]AGAGCAACAGGATGA | 29979 |
rs188745951 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83674671 | AGTTAAGGATGTCAA[C/T]ACTCAATTTAAAAAC | 29979 |
rs188800468 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83681610 | GGCACAATGAACACC[A/G]TATACAAAAAGCACA | 29979 |
rs188802224 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83699858 | GGCACAATAGATTTC[A/C/G]ACTACCAGTTTGCTG | 29979 |
rs188912707 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83702931 | CACTTTCTAAAACCA[C/G]AGTATATACTGCCTG | 29979 |
rs189033197 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83699400 | CAGCTGGAATGCTGC[A/G]GTGCAATCATAGCTC | 29979 |
rs189122211 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83687975 | GATAAGCAATTTCCA[A/G]GTAACTAACAGAAAA | 29979 |
rs189190095 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83662330 | GATAGTTCAGAATTA[A/G]ATGATTTGTGTAGCT | 29979 |
rs189200909 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83694900 | TTAAAGCTCCTTACC[C/T]ATCATCAGATTTCTC | 29979 |
rs189210563 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83700780 | ATGTAGTCAGCCAAG[C/T]AAGCAAAGAAAGAAG | 29979 |
rs189223885 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83705107 | ACACACCCGCTAAAA[C/T]AGCTAAAATTACAGA | 29979 |
rs189370871 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83709452 | CTTTGCCTAGGCTGC[C/T]TTCCTCTACCTAGAA | 29979 |
rs189464563 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83691237 | TGGGCAGGTCAACTG[A/G]AAGGAAATGGAATGA | 29979 |
rs189482864 | snp | A/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83681809 | CACTTCTGGCCAAAG[A/T]ATAGCAGGTTCAACT | 29979 |
rs189523548 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83689401 | GAAACTGACAGACTA[A/C]ATGGGCAAAAATGAA | 29979 |
rs189528888 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83706756 | ATTTGATTGCAACCG[C/T]TAATATCAACATCGC | 29979 |
rs189556459 | snp | A/T | 4.9923e-05 | 0.0049959 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83685996 | CTGTACATCTTCCAA[A/T]ACCATACCTGTTTTG | 29979 |
rs189604720 | snp | G/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83669651 | AAAATTCCATAAAGT[G/T]AAAAGGACTGAGCCA | 29979 |
rs189754277 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83673753 | ACTTTTACAAAAGCA[C/G]TGAGTACTTGCAACA | 29979 |
rs189827475 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | UBQLN1 | GRCh38.p7 | 9:83667334 | CAACTAACAAGGATT[A/T]ACTGATAGCCTATTT | 29979 |
rs189833782 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83704354 | TTCTTCCACATTTTC[C/T]TGTATCTGTTTCCCT | 29979 |
rs189863470 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83673194 | AAGATTATACCACTG[A/C]ACTCCAGCCTGGGCG | 29979 |
rs189863559 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83692381 | CACTAACATTTGAAC[A/G]TAACTTCCTTGTCTG | 29979 |
rs190013571 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83695965 | TTTTTTTTTGAGTCG[C/G]AGTCTCACTCTGTTG | 29979 |
rs190015554 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant, utr-variant-3-prime | UBQLN1 | GRCh38.p7 | 9:83668309 | AACCATTCATTTGAC[A/T]TAAAGCTTTTAAAAT | 29979 |
rs190123295 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83691577 | AGTAGGACACTACAC[C/T]ACACATTCGAAAATT | 29979 |
rs190193088 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83680260 | TAAAATCAACAAAAT[A/G]TATTTTCATGTATGT | 29979 |
rs190193224 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83698443 | ATTTCAAAATGCAAG[A/T]TATTTTATAGTCTTT | 29979 |
rs190448578 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83702363 | GAATCATTAAATAAC[A/G]AGTTTTTCAGCTGTC | 29979 |
rs190517657 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83664294 | TGTGCTGGTGCACAC[C/T]TGTAGTATCAGTTAC | 29979 |
rs190528227 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83683169 | TGTAATCCCAGCACT[C/T]TGGGAGGCCGAAGCT | 29979 |
rs190531351 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83676395 | GACAATCATGGTAAA[C/G]GGAAAGAAAACAACA | 29979 |
rs190630934 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83672514 | GAATAGGGAGACCCA[A/G]GAAGAGGAAGAGAGA | 29979 |
rs190669873 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83678922 | GAGACGGGGTTTCAC[C/T]GTGTTAGCCAGGATG | 29979 |
rs190788919 | snp | A/C | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83679204 | AAGAAAGAGTTCCCT[A/C]CATTTTAACCCTATT | 29979 |
rs190928001 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83697716 | ATGCACCACCACACG[C/T]GGCTATTTTTTGTAC | 29979 |
rs190943875 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83682297 | CTCAAAAAATATATA[C/T]ATATATATTCCACAG | 29979 |
rs190944129 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83662845 | TTGGGAGGCCAAGGC[A/G]GGTGAGATCGCTTGA | 29979 |
rs190948471 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83664812 | TAGTCCCAGCTACTT[A/G]GGAGGCTGAGGTGAG | 29979 |
rs190951820 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83702634 | CATAATATATCAAAA[A/G]TATTAAGATATTTAT | 29979 |
rs191099921 | snp | A/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83688782 | AGGAGAATTGCTTGA[A/T]CCTGGGAGGCAGAGG | 29979 |
rs191199138 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83683916 | ATCACAGGTACTCAG[A/G]AGGCTGAGGCAGGAA | 29979 |
rs191256489 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83671765 | ATAATAAATGAGCAC[C/T]GGCTTCAACTCAGTC | 29979 |
rs191264836 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83690844 | CCCCAAAGCTAAAAT[A/G]TGCCTCAATGGGAGC | 29979 |
rs191344548 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83668966 | ACCTGCACTTCTTTC[C/T]AGTCAATGAATGGCA | 29979 |
rs191358756 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83705301 | GCTGGACTGCAATGT[C/G]GCAATCTCGGCTCAC | 29979 |
rs191383939 | snp | A/C | 0.00398564 | 0.0444627 | upstream-variant-2KB, intron-variant | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83708699 | CTGTATTGACAGTGG[A/C]CTCTGCTGCTACGAT | 29979 |
rs191600098 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83675771 | ACGTATTTTGAATAA[A/G]TCAGTCAAGTCTCAC | 29979 |
rs191612873 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83694340 | CCTTCAAGAGTCTAT[C/T]TTTGAATTAGCTCCT | 29979 |
rs191751694 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83698052 | GCATCTTCATTTTTT[A/T]AAAAAAGGATAATAA | 29979 |
rs191905191 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83685514 | TATCTCTTTAAAACT[A/G]GTGGTGCCAGCTGGA | 29979 |
rs191910704 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83692995 | CTATGTGGTCACTAT[C/T]AACTCAAAATGAAAG | 29979 |
rs191924424 | snp | C/T | 0 | 0 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83703764 | GGAAAAAAGCTTAAG[C/T]TTTATTAGTAACCTT | 29979 |
rs192147738 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83681062 | GACTATGCTTCTAAT[A/G]ATCTTTCCAAAAGAC | 29979 |
rs192207697 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83701476 | TCATGGTACCCTTAA[C/T]AGGGTATGGGGACTC | 29979 |
rs192214472 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83699603 | TGCCACCTTGGCCCC[G/T]CAAAGTGTTGGGATT | 29979 |
rs192217489 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83674486 | TAAAAATGAAAATAA[A/G]ACTGCAACCAAAGTT | 29979 |
rs192288939 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83707103 | TTCATGAAACAAAAC[C/T]GCAGCCTGAGCTAAA | 29979 |
rs192290555 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83681377 | TAAGGCAACAAGAAA[C/G]ACATCCTCAGAACTC | 29979 |
rs192294385 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | UBQLN1 | GRCh38.p7 | 9:83661644 | CCACACATCTTACTG[C/T]ACTCCACCTTAAAAT | 29979 |
rs192443440 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83665888 | CACTGACTATTTTAA[G/T]CTTACTAATCCCGAG | 29979 |
rs192520920 | snp | C/T | 0.0023933 | 0.0345097 | utr-variant-3-prime | UBQLN1 | GRCh38.p7 | 9:83660347 | TTTCCTGTAACTGTA[C/T]ATGAGAGAATATAAT | 29979 |
rs192549346 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83699330 | AATAGGAAAATTACA[C/T]ATGTGGCTCATACTG | 29979 |
rs192556178 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83684298 | CTCCCAGGTTCAAGC[A/G]ATTCTCCTGCCTCAG | 29979 |
rs192558754 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83702991 | TTACACATAACCTAA[C/G]AGTCTATGAAATCCC | 29979 |
rs192738986 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83690086 | AGAAGTTGAACATAT[A/G]CTTACCCTATGACCC | 29979 |
rs192769246 | snp | C/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83686315 | GAGGACTGCCTGAGT[C/G]CAGGAGTTCGAGGCT | 29979 |
rs192804412 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83674763 | CTGCTCAATTGTATG[A/G]GGAGTCAATGGTAAG | 29979 |
rs192942643 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83671077 | CTCAAGGGATCCTCC[G/T]GCCCGAACCTTCCAA | 29979 |
rs192947575 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83708214 | TTTCCAGTTAAGCGC[C/T]GTAACGGCGCACCGA | 29979 |
rs192986076 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83670267 | TCTGCTATTCCATCC[A/G]GTTATATCAGGCTTA | 29979 |
rs193019119 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83693544 | TTTTCTATTTTTAAT[C/G]TGAGGAAGAAGCAGC | 29979 |
rs193200680 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83689874 | GAAATTGAAACAGGA[A/G]TTTCACAAAAATGAA | 29979 |
rs193271581 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83677346 | GGCAGGCGGATCACC[A/T]GAGGTCAGGAGTTCA | 29979 |
rs199675570 | in-del | -/AA | 0.02016 | 0.0983543 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83699748 | AATACCAGGGTAAGC[-/AA]ACTTTCTGTTACGGG | 29979 |
rs199677672 | snp | C/T | 0.000399281 | 0.0141238 | missense | UBQLN1 | GRCh38.p7 | 9:83669315 | TGCATTCCTGGTGTG[C/T]TGAACATACTAGCTG | 29979 |
rs199680794 | in-del | -/A | 0.0599851 | 0.162463 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83684811 | GTGAAATTCCGTCTC[-/A]AAAAAAAAAAAAAAA | 29979 |
rs199777538 | in-del | -/A | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83704515 | CTTCAGAAAGACTTT[-/A]AATTTTATCTATTAA | 29979 |
rs199791521 | snp | C/T | 0.00199792 | 0.0315431 | synonymous-codon, intron-variant | UBQLN1 | GRCh38.p7 | 9:83666353 | TGTCTTACTCACTTG[C/T]TGGAGGAAAGTTGGG | 29979 |
rs199812188 | in-del | -/AA | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83663082 | AAGAAAAAAAAAAAA[-/AA]GGGAAAGGCAAAGAG | 29979 |
rs199821031 | in-del | -/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83696464 | AAACAAACAAAAAAA[-/T]TTTAAAAAAAAACCC | 29979 |
rs199916414 | snp | C/T | | | missense | UBQLN1 | GRCh38.p7 | 9:83661921 | GTTGTTGCTGAAATC[C/T]GACTTCTGGATTCTG | 29979 |
rs199947452 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83670148 | ACTAAGTTAATTTGC[C/T]TGACTCACACCTAGA | 29979 |
rs199985063 | snp | A/G | 0.000150372 | 0.00866969 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83685987 | ATTTTAAAGCTGTAC[A/G]TCTTCCAAAACCATA | 29979 |
rs200100152 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83663070 | AAAGGGAAAGGGAAA[A/G]AAAAAAAAAAAAGGG | 29979 |
rs200151116 | snp | A/G | 0.00174391 | 0.0294773 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83678627 | TTTCCAAAAAAAGAA[A/G]AAAAAAAGGCATTGA | 29979 |
rs200199388 | in-del | -/A | | | intron-variant, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83705937 | TGTAACTTAGGGCAT[-/A]AAAAAAAAAAACTGG | 29979 |
rs200245887 | in-del | -/TG | | | intron-variant, utr-variant-3-prime | UBQLN1 | GRCh38.p7 | 9:83667914 | GTACTAGCAACATTT[-/TG]TTTTAGAGTAAAAAA | 29979 |
rs200269776 | snp | C/G | 1.86284e-05 | 0.00305186 | missense | UBQLN1 | GRCh38.p7 | 9:83686122 | CAAGTTGGTCAGTAT[C/G]TGATTTAAAACGTTT | 29979 |
rs200321955 | in-del | -/AT | 0.192715 | 0.243348 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83691175 | AAACACAATATATAC[-/AT]ATATATATATACACA | 29979 |
rs200324286 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83665199 | AAATCAGTGAACGTA[A/T]ATTTTTAAATCTTTT | 29979 |
rs200350698 | snp | C/T | 0.000399281 | 0.0141238 | missense | UBQLN1 | GRCh38.p7 | 9:83669304 | GCAACAAGCTCTGCA[C/T]TCCTGGTGTGTTGAA | 29979 |
rs200362898 | in-del | -/GAA | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83697759 | TTTTTTTTTTGAGAC[-/GAA]GTCTCACTCTTATCC | 29979 |
rs200482902 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83662275 | ATACATATACATATA[C/T]ACACACACACACACA | 29979 |
rs200519298 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83683437 | AAAAAAAAAAAAAAA[C/T]AACCACTGAAATCCT | 29979 |
rs200748012 | snp | C/T | 0.000362384 | 0.0134559 | missense | UBQLN1 | GRCh38.p7 | 9:83663963 | GCTGTGGGACTTGTG[C/T]TTTCACTAGGTGTGG | 29979 |
rs200810123 | snp | A/G | 5.02525e-05 | 0.00501236 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83683098 | ATCACAGAGTAAGCA[A/G]TAGAGCTGATTATTT | 29979 |
rs200840903 | snp | C/T | 8.18029e-05 | 0.0063949 | missense, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83707646 | CGCTATCCTGGGAGC[C/T]CGGAGGACCGCCGCT | 29979 |
rs200927958 | snp | G/T | 1.64841e-05 | 0.00287085 | missense, intron-variant | UBQLN1 | GRCh38.p7 | 9:83666376 | AAGTTGGGAGCTGTT[G/T]TCTCATTTGTTCTTG | 29979 |
rs200949835 | in-del | -/A | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83696467 | AATTTTAAAAAAAAA[-/A]CCCAATAAGAAAAAT | 29979 |
rs200964068 | snp | A/C | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83700395 | AGTAGTTATTACTGA[A/C]TATGTATTATTGTAC | 29979 |
rs201039961 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83691200 | TACACATATAATACA[C/T]ATATATATATATGCC | 29979 |
rs201060728 | snp | A/C | | | intron-variant, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83706127 | TGCCAAAATTACGTC[A/C]AAAAAACGTAAAAAA | 29979 |
rs201071675 | snp | C/T | 4.94425e-05 | 0.0049718 | missense | UBQLN1 | GRCh38.p7 | 9:83677811 | TAGTGCCACCCACAG[C/T]GCTGGCAGTGCCGCT | 29979 |
rs201074120 | snp | C/G | 0.00199798 | 0.0315436 | utr-variant-3-prime | UBQLN1 | GRCh38.p7 | 9:83661772 | ATTACATTTTTTCAA[C/G]ATACAGAAATGCTGC | 29979 |
rs201191228 | snp | A/T | 1.65509e-05 | 0.00287666 | synonymous-codon | UBQLN1 | GRCh38.p7 | 9:83669269 | GTTTTGCATCAGTTG[A/T]GGGTTTTCAGTTATT | 29979 |
rs201254844 | snp | A/G | 5.0043e-05 | 0.0050019 | synonymous-codon | UBQLN1 | GRCh38.p7 | 9:83677950 | CAAGGAAGCAAATGG[A/G]TTACCACCAAACTGT | 29979 |
rs201285098 | snp | C/T | 0.00199792 | 0.0315431 | missense | UBQLN1 | GRCh38.p7 | 9:83679942 | CCATCATTTCAGGGT[C/T]AGACAAAAGTTGTCG | 29979 |
rs201291599 | snp | A/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83682328 | AACCTCAATATATAA[A/T]TCTAATACAGGCCAG | 29979 |
rs201294210 | in-del | -/ATAC | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83662266 | TGTGTGTATATACAT[-/ATAC]ATATACACACACACA | 29979 |
rs201364133 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83671269 | GTTCATGTTGATATT[C/T]TGACATCCTCTCCAT | 29979 |
rs201410031 | snp | A/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83684830 | AAAAAAAAAAAAAAG[A/T]AAGGAAATAAAAAAA | 29979 |
rs201413272 | in-del | -/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83685153 | AGCACCAAAATAGAA[-/G]GGAATATGTTGAATG | 29979 |
rs201462196 | in-del | -/CAAAA | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83677585 | CAAAACAAAACAAAA[-/CAAAA]GCAACATGAAAAATA | 29979 |
rs201549991 | snp | A/C | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83688861 | AGCGAAACTCCGTTT[A/C]AAAAAAAAAAAAAGA | 29979 |
rs201699870 | snp | C/T | 0.000167224 | 0.00914243 | synonymous-codon | UBQLN1 | GRCh38.p7 | 9:83669188 | TTACAAACTCACCTG[C/T]GCAGCAAGGTCAGGA | 29979 |
rs201718401 | snp | G/T | 0.000633828 | 0.0177908 | missense, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83707617 | GGGGGCGCCAGCACC[G/T]TCGGCTCCGGCGGCG | 29979 |
rs201739392 | snp | A/C | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83703162 | TGATGAACAATTAAC[A/C]AAAAAAAAAAAATCT | 29979 |
rs201765508 | in-del | -/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83695944 | ACTTCACTTTTCAAA[-/T]TAATTTTTTTTTTTG | 29979 |
rs201847758 | snp | G/T | 8.03826e-05 | 0.00633915 | synonymous-codon, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83707587 | GATTTTGGGCTCCGC[G/T]GAGGCAGCGGCCGCG | 29979 |
rs201877595 | snp | C/G | 1.64749e-05 | 0.00287005 | missense | UBQLN1 | GRCh38.p7 | 9:83663960 | CCTGCTGTGGGACTT[C/G]TGTTTTCACTAGGTG | 29979 |
rs201974454 | snp | C/T | 0.00011536 | 0.00759387 | missense | UBQLN1 | GRCh38.p7 | 9:83661827 | CTTTCAATAGCTGCA[C/T]TGATATCACCTCCTG | 29979 |
rs202107766 | snp | A/G | 0.00199806 | 0.0315443 | synonymous-codon | UBQLN1 | GRCh38.p7 | 9:83686065 | TTCCATGCTGACTCA[A/G]GGTATCTTGATCTTT | 29979 |
rs202127388 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83697139 | CAGTTTGGGGCAGTG[A/G]ATCGGTGAGGCCTCC | 29979 |
rs202156565 | snp | A/C | | | missense | UBQLN1 | GRCh38.p7 | 9:83678575 | TCTCCTGCATCATTG[A/C]TGGATTCCTGGCAAG | 29979 |
rs202159303 | in-del | -/A | | | utr-variant-3-prime | UBQLN1 | GRCh38.p7 | 9:83661613 | ACTGTTCCAGAAAAG[-/A]AAAATACAGAAAAAC | 29979 |
rs202217041 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83679678 | ATTTCTCTCTTTAGC[C/T]TAACCATACATACAG | 29979 |
rs367572209 | in-del | -/AAG | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83674242 | CAAGAAAAAAGGAAG[-/AAG]GAGAGTTACAAATGT | 29979 |
rs367707607 | snp | C/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83666151 | TTCCTCAGAATGTAT[C/G]TTTAAGAAACATAAG | 29979 |
rs367779906 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83680625 | ACCTGGATGGAACCT[C/T]TGAGCCCAACTTCCA | 29979 |
rs367828979 | snp | A/T | 1.67223e-05 | 0.00289151 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83664072 | AAATAGGAAATATCC[A/T]AAGGTCCTGCAAAAC | 29979 |
rs367843701 | snp | A/G | 9.06627e-05 | 0.00673224 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83677714 | AAAAAAGCCTGAGTT[A/G]TTAAAAGCATACCTC | 29979 |
rs367867985 | snp | A/C | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83709124 | ACTGTTACATAAACA[A/C]GACTTTTTAGCAGAG | 29979 |
rs367887071 | snp | A/G | 1.64803e-05 | 0.00287052 | missense | UBQLN1 | GRCh38.p7 | 9:83677897 | CTATTTTCTGTACGG[A/G]AAGGTTGACTACCTT | 29979 |
rs368001490 | snp | G/T | 3.30246e-05 | 0.0040634 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83666326 | AATCATTACCCAAGA[G/T]AGCTAACATCTTGTC | 29979 |
rs368006033 | in-del | -/A | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83680464 | AGACAAAGTGATTAA[-/A]GGGCTAAAACTTTCA | 29979 |
rs368015830 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83664563 | TCAAGTTCAGCCAGG[A/G]TAAAAGAGCAAAAAC | 29979 |
rs368033867 | snp | A/T | 0.00106777 | 0.0230813 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83664067 | AGCACAAATAGGAAA[A/T]ATCCTAAGGTCCTGC | 29979 |
rs368067353 | in-del | -/C | 0.00398564 | 0.0444627 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83666610 | GGATCTCCAGAAGAA[-/C]AAAAACAAAAAAATG | 29979 |
rs368113978 | snp | A/C | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83695199 | TGAATGGGCCCTCCC[A/C]CCTTTTTTTTTTTTT | 29979 |
rs368215423 | snp | A/G | | | utr-variant-3-prime | UBQLN1 | GRCh38.p7 | 9:83660657 | TCCAGGACAGATTCC[A/G]CTGCCCCACCCCCCC | 29979 |
rs368241581 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83700563 | AAAACAGGCTACTGT[A/G]AGAAATCCAACAGGG | 29979 |
rs368258483 | in-del | -/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83705666 | GACCACAAAAAGACT[-/T]GTATAAGACTGTTCA | 29979 |
rs368334248 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83682097 | AGACCATCCTGGCTA[A/G]TATGGTGAAACCCAG | 29979 |
rs368436575 | snp | G/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83668997 | GAGATAAAGTTGTTT[G/T]AATTACATATGAAGT | 29979 |
rs368472277 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83671426 | CTTAAATAAGACTTG[A/T]AAGTTGAAAGTGCTC | 29979 |
rs368496052 | in-del | -/TGGA | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83697787 | TCTTATCCCACAGGC[-/TGGA]TGGAGTGCGATGGCA | 29979 |
rs368560665 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83664873 | GCAGTGAGCCACAAC[C/T]GCGCCCCCACACTCA | 29979 |
rs368582363 | snp | C/T | 1.68281e-05 | 0.00290065 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83663837 | TCTAAATTTCCAACA[C/T]TAAGGAATACAAAAC | 29979 |
rs368598673 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83696220 | TTATAAAGTACAACA[C/T]GATGTCTTGATATAT | 29979 |
rs368644266 | snp | C/T | | | utr-variant-3-prime | UBQLN1 | GRCh38.p7 | 9:83661374 | TTGCAAAAATGCATG[C/T]CAAAGTCACAATAAG | 29979 |
rs368661799 | snp | A/G | 3.34582e-05 | 0.00408999 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83685985 | CAATTTTAAAGCTGT[A/G]CATCTTCCAAAACCA | 29979 |
rs368669505 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83684928 | AAGGCACACATTTTT[C/T]TATTTTAACATCTCC | 29979 |
rs368669647 | snp | A/C | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83680387 | ACAAGCCCTTTTGAT[A/C]ATTATGCTAATGAAG | 29979 |
rs368676425 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83705746 | AATTATGGTATACAC[A/G]TACAGTGGAAAACTA | 29979 |
rs368696422 | snp | A/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83698515 | AATAAAGCATATTAA[A/T]ATTACAATAGCCAAA | 29979 |
rs368742478 | snp | C/T | 5.04494e-05 | 0.00502217 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83678407 | TTAAAACAGAAGCTA[C/T]TCCTTGGCCTGAACC | 29979 |
rs368869937 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83669151 | TATTTTAATTCACAC[C/T]GCACAGTCTTTTTCA | 29979 |
rs368946167 | snp | A/C | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83666296 | AAAATGTTTATCATC[A/C]AATTTTTTCAAGCAA | 29979 |
rs368967836 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83684679 | AGCCGGGCGTGGTGG[C/T]GCATGCCTGTAATTC | 29979 |
rs368977783 | snp | C/T | | | intron-variant, downstream-variant-500B | UBQLN1 | GRCh38.p7 | 9:83667486 | ATTTCAATACAATAA[C/T]AAAAGCAGATGTCAG | 29979 |
rs369082920 | snp | A/T | 0.00018282 | 0.00955911 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83678630 | CCAAAAAAAGAAAAA[A/T]AAAAGGCATTGAAAT | 29979 |
rs369157308 | snp | A/C | | | upstream-variant-2KB, intron-variant | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83708711 | TGGCCTCTGCTGCTA[A/C]GATGACAGCTGTGCG | 29979 |
rs369236712 | snp | C/T | 1.64735e-05 | 0.00286993 | missense | UBQLN1 | GRCh38.p7 | 9:83678555 | TCGGTCCTGGTTCCT[C/T]ATCATCTCCTGCATC | 29979 |
rs369266095 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83670809 | AAACATTCTGAATTC[A/G]TTGTCATTTCAATAA | 29979 |
rs369290028 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83661960 | AAAGAAAAAAAAAAT[C/T]AATCCAACTCTAAAG | 29979 |
rs369310881 | snp | C/T | 0.00636936 | 0.0560724 | utr-variant-3-prime | UBQLN1 | GRCh38.p7 | 9:83660189 | TCCTCCTGGGGAAAG[C/T]GTCAGAACAGTGCAA | 29979 |
rs369384141 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83694662 | ACAAACTAAATGTTT[C/T]ACTATTCACATGCTA | 29979 |
rs369404306 | snp | A/C | | | upstream-variant-2KB, intron-variant | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83709664 | AATTATCTGTGTCTA[A/C]ATTATTGTCTAAAAA | 29979 |
rs369456025 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83692557 | AACTTATTACAATTA[C/T]ACAAAATATTTTCGG | 29979 |
rs369619605 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83674109 | ACACCTGGCCTCCTT[C/T]GTACTGTTGTTCAGT | 29979 |
rs369808992 | snp | A/G | 1.65312e-05 | 0.00287495 | missense | UBQLN1 | GRCh38.p7 | 9:83680023 | TACTCAGACCTGCAA[A/G]TCCCCCAAGGCCACC | 29979 |
rs369817458 | snp | C/G | 4.94442e-05 | 0.00497188 | synonymous-codon | UBQLN1 | GRCh38.p7 | 9:83665092 | CTGAATCTGTAACAA[C/G]GCCTGCATTGCTCTA | 29979 |
rs369893953 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83690057 | CAGTACATTTTGGAA[C/T]AACATTTTGCAACAG | 29979 |
rs369917856 | snp | C/T | 3.4443e-05 | 0.00414973 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83665004 | AACCATTATACACTT[C/T]CATTATCTTCCCCAA | 29979 |
rs370014547 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83666239 | TGACAGCATTATTGG[A/T]CTCTATTCTATGTTT | 29979 |
rs370104999 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83698640 | AATTCTGGCTGGGTG[C/T]GGTGGCTCACACTTG | 29979 |
rs370125403 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83683179 | GCACTTTGGGAGGCC[A/G]AAGCTGGCTGATCAC | 29979 |
rs370231025 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83703963 | ATTACAGCATGTTCA[C/T]ATAAACAGAATTTTG | 29979 |
rs370268242 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83673341 | GTCGGGAGTTTGAGA[A/C]CAGCCTGGCCAACAT | 29979 |
rs370271248 | snp | A/G | 3.3539e-05 | 0.00409492 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83685980 | ATCCACAATTTTAAA[A/G]CTGTACATCTTCCAA | 29979 |
rs370280147 | snp | C/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83669925 | AACCCATGTGATCTT[C/G]GGCAAGTTATCTAGC | 29979 |
rs370292077 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83702024 | CTTCAACAGGGATGA[A/T]CCTTGAAAACACTAT | 29979 |
rs370305042 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83677432 | CCGGGCATGGTGGCA[A/G]GTGCCTGTAATCCCA | 29979 |
rs370436678 | snp | C/T | 1.65745e-05 | 0.00287871 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83679767 | AACTGAAAGAACTTT[C/T]CACATACTTGTCTCA | 29979 |
rs370508683 | snp | C/T | 0.000115326 | 0.00759274 | synonymous-codon | UBQLN1 | GRCh38.p7 | 9:83677875 | CCATGGATTGGGTAG[C/T]GGATCTCTATTTTCT | 29979 |
rs370516689 | in-del | -/AT | 0.288386 | 0.247035 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83682289 | ACTCTGTCTCAAAAA[-/AT]ATATATATATATATA | 29979 |
rs370539805 | in-del | -/AC | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83662274 | TATACATATACATAT[-/AC]ACACACACACACACA | 29979 |
rs370560589 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83704299 | CTTTTGTGCTTCAAG[C/T]AGATTTTACAAATAG | 29979 |
rs370564077 | snp | C/T | | | utr-variant-3-prime | UBQLN1 | GRCh38.p7 | 9:83659968 | GCAAGACAAATCAAG[C/T]GTAAAAGCTAGAGAT | 29979 |
rs370577013 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83670792 | TATCAACAAAGTTTA[C/T]GAAACATTCTGAATT | 29979 |
rs370672566 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83701559 | GCAGGCTGTCCAGTT[C/T]TCCTCAGAGTGCCCC | 29979 |
rs370680888 | snp | A/G | | | utr-variant-3-prime | UBQLN1 | GRCh38.p7 | 9:83660808 | GTGCATGAGAAAACA[A/G]ATAAACCCAAAAGAT | 29979 |
rs370694207 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83695328 | CTCAGCCTCCCAGGT[A/G]GCTGGGACTACAGGT | 29979 |
rs370703138 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83677051 | TCCACAAAGTCTGAG[A/G]GTAAGATCTGGGAAT | 29979 |
rs370787248 | in-del | -/A | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83685329 | TACTGTATGAAAAAA[-/A]TATGGACACTGACAA | 29979 |
rs370916771 | snp | A/G/T | 0.00199481 | 0.0315187 | upstream-variant-2KB, intron-variant, nc-transcript-variant | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83708336 | CCCACCTTACCTCAT[A/G/T]CCCAGCTGGGCCGTG | 29979 |
rs370957284 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83696033 | CAACCTCCACCTCCC[A/G]GATTCAAGCGATTCT | 29979 |
rs370971326 | snp | A/G | 0.000218119 | 0.0104409 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83683101 | ACAGAGTAAGCAGTA[A/G]AGCTGATTATTTTTA | 29979 |
rs370976050 | in-del | -/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83695945 | CTTCACTTTTCAAAT[-/T]AATTTTTTTTTTTGA | 29979 |
rs371018804 | in-del | -/A | 0.0182102 | 0.093667 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83678625 | TATTTCCAAAAAAAG[-/A]AAAAAAAAAGGCATT | 29979 |
rs371058649 | snp | A/T | 2.03705e-05 | 0.00319137 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83677704 | GACAACAAAGAAAAA[A/T]GCCTGAGTTGTTAAA | 29979 |
rs371101480 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83681909 | GACTTTCATTAGCTT[A/G]AGTCTCTGAGGGACT | 29979 |
rs371158647 | in-del | -/C | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83699965 | TATCTTGAAATCTGC[-/C]ACAGTGAGAATATTT | 29979 |
rs371278505 | in-del | -/TT | 0.00199481 | 0.0315187 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83687913 | GCTTTTCCATCTGCA[-/TT]CTTTCCTTTATTTGA | 29979 |
rs371320587 | snp | C/T | 1.6641e-05 | 0.00288448 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83664056 | AACCTACAGAAAGCA[C/T]AAATAGGAAATATCC | 29979 |
rs371350777 | snp | A/C | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83665556 | AATATAACAATTTTA[A/C]CAGTAAGGTACACTC | 29979 |
rs371405912 | snp | A/C | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83676581 | TCAGGTTTTACAAAA[A/C]CTATATTATAAACAT | 29979 |
rs371521089 | snp | C/T | | | upstream-variant-2KB, intron-variant | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83709720 | GTAATAAGATTTACC[C/T]GTAAGAAGATACCAT | 29979 |
rs371557921 | snp | C/T | 6.68818e-05 | 0.00578242 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83664071 | CAAATAGGAAATATC[C/T]TAAGGTCCTGCAAAA | 29979 |
rs371575122 | snp | A/G | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83682654 | TATTCAGGGACGCTG[A/G]CTTACGATTAATAAC | 29979 |
rs371589345 | snp | C/T | 1.65869e-05 | 0.00287979 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83665026 | CTTCCCCAAATAAGC[C/T]TACCCTGGGATGAGG | 29979 |
rs371636780 | snp | C/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83697280 | GACATAGGCCAGGCG[C/T]GGTGGCTCACGCCTG | 29979 |
rs371640759 | snp | G/T | | | intron-variant | UBQLN1 | GRCh38.p7 | 9:83678894 | CGCTAATTTTTTTTT[G/T]TATTTTTTAGTAGAG | 29979 |
rs371649581 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBQLN1 | GRCh38.p7 | 9:83669839 | GTAGGCACATTTAAC[A/G]TTTGAAACCATAGAG | 29979 |
rs371734056 | snp | G/T | | | intron-variant, upstream-variant-2KB | UBQLN1, LOC105376114 | GRCh38.p7 | 9:83706040 | TGTTCTATATCTTGA[G/T]AAGAGCTTGGGCTAC | 29979 |