SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs731237 | snp | C/G | 0 | 0 | intron-variant, upstream-variant-2KB | USP5, CDCA3 | GRCh38.p7 | 12:6852635 | GGCAGTCGGCCTTGT[C/G]TGCCGCGCACGGCTC | 8078 |
rs743599 | snp | C/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | USP5, CDCA3 | GRCh38.p7 | 12:6853136 | ATGTCACCCTCAAGC[C/G]GAGGCCCTTTGGGGC | 8078 |
rs1076865 | snp | C/T | 0.263181 | 0.249652 | intron-variant, upstream-variant-2KB | USP5, CDCA3 | GRCh38.p7 | 12:6853814 | TAGAGCATTTCTCAC[C/T]GGGGAGGTCAACTAA | 8078 |
rs1076866 | snp | C/T | 0.00943375 | 0.0680285 | intron-variant, upstream-variant-2KB | USP5, CDCA3 | GRCh38.p7 | 12:6853980 | TTGAGCAACAACAGA[C/T]ATCCTCTTCCAGGAA | 8078 |
rs1126996 | snp | A/G | 6.58924e-05 | 0.0057395 | synonymous-codon, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6859512 | CCAGAATGCCCCGAC[A/G]GACCCTACCCAGGAT | 8078 |
rs1802898 | snp | C/T | | | missense, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6861076 | TACATCATGCAGCTG[C/T]CTGTGCCCATGGATG | 8078 |
rs2071058 | snp | A/T | 0.497566 | 0.0347987 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | USP5, CDCA3 | GRCh38.p7 | 12:6851729 | CTGGATACCCCCTTT[A/T]CAAATACCAAGACAA | 8078 |
rs2071059 | snp | A/G | 0.442197 | 0.159876 | intron-variant | USP5 | GRCh38.p7 | 12:6860567 | CCCATTTCTCCCTCT[A/G]TCAGCCCCAACCCAG | 8078 |
rs2071060 | snp | A/C | 0.0239773 | 0.106835 | intron-variant, downstream-variant-500B | USP5 | GRCh38.p7 | 12:6864473 | GGTGGGCGGATCACG[A/C]GGTCAGCAGATCAAG | 8078 |
rs2071061 | snp | A/G | 0.277778 | 0.248452 | intron-variant, downstream-variant-500B | USP5 | GRCh38.p7 | 12:6864487 | GCGGTCAGCAGATCA[A/G]GACCATCCTGGCTAA | 8078 |
rs2071062 | snp | C/T | 0.5 | 0 | intron-variant, downstream-variant-500B | USP5 | GRCh38.p7 | 12:6864557 | AACCAAGCGTGGTGG[C/T]GGGCGTCTGTAGTCC | 8078 |
rs2071063 | snp | A/T | 0.0232526 | 0.105288 | intron-variant, downstream-variant-500B | USP5 | GRCh38.p7 | 12:6864602 | GCTGAGGCAGGAGAA[A/T]GGCGTGAACCCGGGA | 8078 |
rs2071064 | snp | C/T | 0.230067 | 0.249204 | upstream-variant-2KB, utr-variant-3-prime | TPI1, USP5 | GRCh38.p7 | 12:6866342 | CCCTGCCCCCGGAAT[C/T]CACAGTGCTCTGCTT | 8078 |
rs2226955 | snp | A/G | 0.463417 | 0.130205 | synonymous-codon, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6856030 | AGGTGTTGAAGGCGG[A/G]TTTGACCTTAGCGAG | 8078 |
rs2238114 | snp | A/C | 0.491493 | 0.0646602 | intron-variant | USP5 | GRCh38.p7 | 12:6856576 | GCTTGGAAATGAACA[A/C]GACATGGGGATGGCC | 8078 |
rs2269356 | snp | A/G | 0.18176 | 0.243942 | intron-variant, upstream-variant-2KB | USP5, CDCA3 | GRCh38.p7 | 12:6852447 | TGCCTTTCATTAACT[A/G]CGGCTGTCGTGTGAC | 8078 |
rs3182461 | snp | A/C | 0 | 0 | upstream-variant-2KB, utr-variant-3-prime | TPI1, USP5 | GRCh38.p7 | 12:6866604 | AAAATGCCAAAATAC[A/C]CGATGTGAATAAAAG | 8078 |
rs4334119 | snp | A/C | 0.203509 | 0.245639 | upstream-variant-2KB, intron-variant | TPI1, USP5 | GRCh38.p7 | 12:6866863 | TCCACTCCTGTGTGA[A/C]TAAAGAGAGGGAAGG | 8078 |
rs5796253 | in-del | -/CA/TG | | | upstream-variant-2KB, intron-variant | USP5, CDCA3 | GRCh38.p7 | 12:6850161 | CACACACACACACAA[-/CA/TG]AAAGCACGGTGGCAT | 8078 |
rs7976501 | snp | A/G | 0.0413113 | 0.137656 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | USP5, CDCA3 | GRCh38.p7 | 12:6851860 | GAATGGACTCTAAGG[A/G]TCCCGGAGCCGGAGC | 8078 |
rs10744719 | snp | C/T | 0 | 0 | intron-variant | USP5 | GRCh38.p7 | 12:6854954 | GTCTTTCCTCTCCCA[C/T]GAAGGGACCCTTTTT | 8078 |
rs10744720 | snp | C/T | 0.131423 | 0.22009 | intron-variant | USP5 | GRCh38.p7 | 12:6855049 | CTGTTAGCCCCAGGA[C/T]AGAGGTGAAGGAAGT | 8078 |
rs11064431 | snp | C/G | 0.236032 | 0.24961 | intron-variant | USP5 | GRCh38.p7 | 12:6854375 | ACAAGTCATTGTTCC[C/G]CTGGAAGCCACACTT | 8078 |
rs11064432 | snp | C/G | 0.261687 | 0.249733 | intron-variant | USP5 | GRCh38.p7 | 12:6859577 | TAGGAAAGCTGTTGA[C/G]AGTCATGGCCGTATA | 8078 |
rs11064433 | snp | A/G | 0 | 0 | intron-variant, downstream-variant-500B | USP5 | GRCh38.p7 | 12:6864353 | GGAGCTGAAGCCTGC[A/G]TTCACTGCTGGGTTT | 8078 |
rs11551593 | snp | A/C | | | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | USP5, CDCA3 | GRCh38.p7 | 12:6851865 | CAGCTGCTCCGGCTC[A/C]GGGACCCTTAGAGTC | 8078 |
rs11609766 | snp | A/C | | | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | USP5, CDCA3 | GRCh38.p7 | 12:6851912 | GCAACCCCGAAGCCC[A/C]CCTAGCTGCTCTACG | 8078 |
rs11612543 | snp | A/G | 0.110497 | 0.207458 | intron-variant | USP5 | GRCh38.p7 | 12:6858737 | AGAGTAGTTCCTATC[A/G]GCTGGGTGTGTTGGC | 8078 |
rs11830318 | snp | A/C | 0.0434404 | 0.14083 | intron-variant | USP5 | GRCh38.p7 | 12:6860538 | TTCCTGCAATTTACT[A/C]GCTCTCCTTCCTGCC | 8078 |
rs11832410 | snp | C/T | | | intron-variant | USP5 | GRCh38.p7 | 12:6858836 | ccagcctgggcaaca[C/T]agcgagaccctgtct | 8078 |
rs11832671 | snp | A/G | 0.0917839 | 0.193566 | intron-variant | USP5 | GRCh38.p7 | 12:6860308 | CTGGGAGATGTCTAA[A/G]GAAGGCCCCTGGATG | 8078 |
rs12302749 | snp | C/T | 0.43634 | 0.166666 | upstream-variant-2KB, intron-variant | TPI1, USP5 | GRCh38.p7 | 12:6867132 | AAGGAGGTTGTCTAT[C/T]CCACAGTTGGAGAGG | 8078 |
rs12824102 | snp | C/T | 0.0465639 | 0.145306 | synonymous-codon, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6863924 | CTACACGGGCAACAG[C/T]GGGGCTGAGGCCGCC | 8078 |
rs16932955 | snp | A/G | 0.022469 | 0.103584 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | USP5, CDCA3 | GRCh38.p7 | 12:6851508 | GCCTGCGAGCCGTCC[A/G]TGGCAGGCTGAGGAG | 8078 |
rs17788417 | snp | C/T | 0.00986232 | 0.0695262 | intron-variant | USP5 | GRCh38.p7 | 12:6860315 | ATGTCTAAAGAAGGC[C/T]CCTGGATGGCCACTG | 8078 |
rs17790720 | snp | C/T | 0.0546152 | 0.155964 | intron-variant | USP5 | GRCh38.p7 | 12:6860824 | ATTAGGGAAGGTTTC[C/T]GCTCTGCTCTTGTGT | 8078 |
rs35165406 | snp | A/G | 0.0138207 | 0.0819715 | synonymous-codon, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6863250 | CAGCTCCTCCTCTCC[A/G]GGCTGCAGCCCTGTG | 8078 |
rs56405548 | snp | A/C | | | intron-variant | USP5 | GRCh38.p7 | 12:6858323 | GTAATTCCACAAATT[A/C]TAGGCCACAGTTGAG | 8078 |
rs58321642 | snp | C/T | 0.5 | 0 | intron-variant | USP5 | GRCh38.p7 | 12:6859101 | AGGAGGGGGGCTTGG[C/T]ACACTAAGAATAAAG | 8078 |
rs60219247 | snp | C/T | 0.5 | 0 | upstream-variant-2KB, intron-variant | TPI1, USP5 | GRCh38.p7 | 12:6866740 | TGCCAAAGTCAAGTC[C/T]CCACTTTTCACTGGT | 8078 |
rs60975689 | snp | A/G | 0.5 | 0 | intron-variant | USP5 | GRCh38.p7 | 12:6859221 | TAGAACGTGAACTGC[A/G]CTTATCCTAATCCCA | 8078 |
rs61607719 | snp | C/G | | | intron-variant, downstream-variant-500B | USP5 | GRCh38.p7 | 12:6864612 | GAGAAAGGCGTGAAC[C/G]CGGGAGGCGGAGCTT | 8078 |
rs61761597 | snp | C/T | 0.000131917 | 0.00812043 | missense, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6863248 | GGCACAGGGCTGCAG[C/T]CCGGAGAGGAGGAGC | 8078 |
rs61916318 | snp | A/T | | | intron-variant | USP5 | GRCh38.p7 | 12:6859818 | CCACCACGCCCAGCT[A/T]AATTTTTTTTGTATT | 8078 |
rs66621175 | snp | C/T | 0.444444 | 0.157135 | intron-variant | USP5 | GRCh38.p7 | 12:6856641 | GGGCCTGCAGAGCCC[C/T]CTCTCTCTGCCACTC | 8078 |
rs72653460 | snp | C/T | 0.299444 | 0.245062 | intron-variant | USP5 | GRCh38.p7 | 12:6858681 | CTGGGCATACTCCTC[C/T]TTCAGCTTCCCTCAG | 8078 |
rs73260817 | snp | A/C | 0.5 | 0 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | USP5, CDCA3 | GRCh38.p7 | 12:6851694 | AGTCACTCGACACAA[A/C]CCCCTCAAGCTCCGC | 8078 |
rs73260823 | snp | A/G | 0.0333766 | 0.124797 | intron-variant | USP5 | GRCh38.p7 | 12:6855371 | CTTCATAACATCCTC[A/G]TGTTTTCACCCTTAC | 8078 |
rs73260825 | snp | C/T | 0.444444 | 0.157135 | intron-variant | USP5 | GRCh38.p7 | 12:6857393 | CTTATCCTATACAGG[C/T]AGAATCAGAATCACA | 8078 |
rs73260833 | snp | A/G | 0.5 | 0 | intron-variant | USP5 | GRCh38.p7 | 12:6860079 | GGGAGAGCCACGAGC[A/G]GGGGGTTGAGCTGGG | 8078 |
rs73260840 | snp | C/T | 0.5 | 0 | upstream-variant-2KB, intron-variant | TPI1, USP5 | GRCh38.p7 | 12:6865809 | AGACATAATAGGGTC[C/T]GTGACCCTTGTGAGG | 8078 |
rs74505435 | snp | C/T | 0.5 | 0 | intron-variant | USP5 | GRCh38.p7 | 12:6859610 | TTCCTCCTCCCTGAC[C/T]GCCTGGGGGGCACAG | 8078 |
rs76061250 | snp | A/T | 0.5 | 0 | upstream-variant-2KB, intron-variant | USP5, CDCA3 | GRCh38.p7 | 12:6850193 | TGTTATGTGTGTGTA[A/T]TTTTTCTAGAGATGG | 8078 |
rs76083908 | snp | C/T | 0.0133132 | 0.0804944 | synonymous-codon, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6860158 | TAATGCAGGGCCAAG[C/T]TGGGCCATGGCCTTC | 8078 |
rs77625565 | snp | C/G | | | intron-variant, upstream-variant-2KB | USP5, TPI1 | GRCh38.p7 | 12:6865473 | TCACTATGTTGCCCA[C/G]GCTGGTCTTGAACTC | 8078 |
rs78059433 | snp | A/G | 0.04875 | 0.148319 | upstream-variant-2KB, utr-variant-3-prime | TPI1, USP5 | GRCh38.p7 | 12:6866606 | AATGCCAAAATACAC[A/G]ATGTGAATAAAAGTA | 8078 |
rs78835987 | snp | C/G | 0.0350586 | 0.127672 | intron-variant, downstream-variant-500B | USP5 | GRCh38.p7 | 12:6864241 | CCAGTGGGGAAGAAG[C/G]GGGTGGGAATGAGGG | 8078 |
rs79239224 | snp | A/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | USP5, TPI1 | GRCh38.p7 | 12:6865444 | CAGCTTTTTTTTTAA[A/T]TAGAGATGGGATCTC | 8078 |
rs79430235 | snp | A/C | 0.000191543 | 0.0097844 | missense, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6861475 | GAGGAGAAGAAGCGG[A/C]AAGCCGAAGAGGAGA | 8078 |
rs79451772 | snp | A/G | 0.000414212 | 0.0143852 | synonymous-codon, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6860461 | GCAGGATGCCCAGGA[A/G]TTCTTCCTTCACCTT | 8078 |
rs111457078 | snp | A/G | 0.48 | 0.0979796 | intron-variant | USP5 | GRCh38.p7 | 12:6859789 | TCCTGAGTAGCTAGG[A/G]CTACAGGCACATGCC | 8078 |
rs111560611 | snp | C/T | 0.5 | 0 | intron-variant | USP5 | GRCh38.p7 | 12:6854195 | TCTCAGCAAGTGTTG[C/T]GAGATTGTTGTCAGA | 8078 |
rs111601142 | snp | A/G | 0.5 | 0 | intron-variant | USP5 | GRCh38.p7 | 12:6863439 | GCCTCTCTGCCTTGC[A/G]TCCCCTGCCCCTGTC | 8078 |
rs112029690 | snp | A/G | 0.000577997 | 0.0169901 | intron-variant | USP5 | GRCh38.p7 | 12:6861642 | CTGGTCGGGGCCTGA[A/G]GCTGTGGGTCTATGG | 8078 |
rs112218165 | snp | C/T | 0.5 | 0 | intron-variant | USP5 | GRCh38.p7 | 12:6859906 | GTGGTCTGCCCACCT[C/T]GGCCTCCCAAAGTGC | 8078 |
rs112300530 | snp | C/G/T | 0.00668249 | 0.0574159 | intron-variant, downstream-variant-500B | USP5 | GRCh38.p7 | 12:6864217 | GCTGCCCCAGCTAAG[C/G/T]ACATGGGGCCAGTGG | 8078 |
rs112306827 | snp | A/G | 0.5 | 0 | intron-variant | USP5 | GRCh38.p7 | 12:6858858 | ACCCTGTCTTCTCTT[A/G]AAAAAAAAAAAGAAT | 8078 |
rs112511011 | snp | A/G | 0.5 | 0 | intron-variant | USP5 | GRCh38.p7 | 12:6854474 | AGAAAGGTCTTTTTC[A/G]CTGGATGTTTAGTCT | 8078 |
rs112562622 | snp | A/G | 0.5 | 0 | intron-variant | USP5 | GRCh38.p7 | 12:6861259 | AGGTAGATTAACCTC[A/G]TCCAGTGGACACTCA | 8078 |
rs112657515 | snp | A/C/G | 0 | 0 | splice-acceptor-variant | USP5 | GRCh38.p7 | 12:6859469 | TTCCCTTGACTTTTA[A/C/G]GTATGTGGATAAGCT | 8078 |
rs112930588 | snp | C/T | 0.00229659 | 0.0338086 | intron-variant | USP5 | GRCh38.p7 | 12:6860511 | GGGCTGGCAAGATGG[C/T]ACACCCCCATCTTCC | 8078 |
rs113032589 | snp | C/T | 0.5 | 0 | intron-variant | USP5 | GRCh38.p7 | 12:6854681 | AAGGATCACTTGAGC[C/T]GGGGAGGTTGAGGCT | 8078 |
rs113045682 | snp | C/T | 0.5 | 0 | intron-variant | USP5 | GRCh38.p7 | 12:6855151 | GCTGTTGAATGGCGA[C/T]GATGAGCTGGTGTTC | 8078 |
rs113090296 | snp | A/T | 0.5 | 0 | intron-variant, downstream-variant-500B | USP5 | GRCh38.p7 | 12:6864581 | GTAGTCCCAGCTACT[A/T]GGGAGGCTGAGGCAG | 8078 |
rs113159521 | snp | A/G | 0 | 0 | intron-variant, downstream-variant-500B | USP5 | GRCh38.p7 | 12:6864422 | TGGCCGGGCGCGGTG[A/G]CTCACGCCTGTAATC | 8078 |
rs113206881 | snp | C/T | 0 | 0 | intron-variant | USP5 | GRCh38.p7 | 12:6861304 | CTGCATGGAAACAGG[C/T]GAGATATATTGGACA | 8078 |
rs113208756 | in-del | -/A | 0.5 | 0 | intron-variant | USP5 | GRCh38.p7 | 12:6858858 | ACCCTGTCTTCTCTT[-/A]AAAAAAAAAAAGAAT | 8078 |
rs113356469 | snp | A/C | 0.5 | 0 | intron-variant | USP5 | GRCh38.p7 | 12:6859203 | TCAACAGGTTCTGTC[A/C]AATAGAACGTGAACT | 8078 |
rs113502733 | snp | C/G | 0.5 | 0 | upstream-variant-2KB, intron-variant | TPI1, USP5 | GRCh38.p7 | 12:6866919 | CTAGCTGGCTTCAGG[C/G]TGGGACTCAGTCCCT | 8078 |
rs113542671 | snp | A/G/T | 0 | 0 | upstream-variant-2KB, splice-acceptor-variant, intron-variant | USP5, CDCA3 | GRCh38.p7 | 12:6851011 | CGAGGAGGGAATGCC[A/G/T]GTGAGAAGTGACTCA | 8078 |
rs113561440 | snp | A/G | 0.5 | 0 | intron-variant, downstream-variant-500B | USP5 | GRCh38.p7 | 12:6864465 | GAGGGTGAGGTGGGC[A/G]GATCACGCGGTCAGC | 8078 |
rs113655717 | snp | C/G | 0.5 | 0 | intron-variant | USP5 | GRCh38.p7 | 12:6859743 | CTACAACCTCTGCCT[C/G]CTGGGTTCAAGTGAT | 8078 |
rs113823591 | snp | C/G | 0.5 | 0 | intron-variant | USP5 | GRCh38.p7 | 12:6862766 | GATTTACAACCAAAA[C/G]TGATTTTTGTAGTTT | 8078 |
rs113894137 | snp | A/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | USP5, CDCA3 | GRCh38.p7 | 12:6853455 | AAAAGAGCACTGCGC[A/G]GAGCAGAGCTCCGGG | 8078 |
rs114210148 | snp | C/T | | | intron-variant | USP5 | GRCh38.p7 | 12:6858346 | CAGTTGAGTATCATC[C/T]TAGACTCAGTGAGAG | 8078 |
rs114350224 | snp | A/G | 0.000313255 | 0.0125112 | synonymous-codon, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6857681 | CCCCAGCCTGGCTGA[A/G]CACCTGTCCCACTTC | 8078 |
rs114768694 | snp | C/T | 0.0654984 | 0.168698 | intron-variant | USP5 | GRCh38.p7 | 12:6862254 | CCTGGGCTTTTTTCT[C/T]TTTCTTTTTTTTGTT | 8078 |
rs114840368 | snp | A/G | 0.096524 | 0.197345 | intron-variant, upstream-variant-2KB | USP5, CDCA3 | GRCh38.p7 | 12:6853756 | GCTAACCAACTTCCA[A/G]CATATTTGGTTACCT | 8078 |
rs114987450 | snp | A/C | 0.0333238 | 0.124705 | intron-variant, upstream-variant-2KB | USP5, CDCA3 | GRCh38.p7 | 12:6853933 | TTTTTCATATCACAG[A/C]AGAGAAATGTTCAAG | 8078 |
rs115270213 | snp | A/G | 0.0333238 | 0.124705 | intron-variant | USP5 | GRCh38.p7 | 12:6856244 | AAGCTGAAGGCCAAG[A/G]GGAAGAGGGGCATGT | 8078 |
rs115306507 | snp | A/C | 0.00398963 | 0.0444848 | intron-variant | USP5 | GRCh38.p7 | 12:6857601 | CCTGAGCCACTTCCC[A/C]TGATTCTCTTCCTGC | 8078 |
rs115578303 | snp | C/G | 0.0333238 | 0.124705 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | USP5, CDCA3 | GRCh38.p7 | 12:6852036 | GGCGGAGCACCGGCA[C/G]GCAGGCTCCGTCCAA | 8078 |
rs115612078 | snp | C/T | 0.00214518 | 0.0326801 | synonymous-codon, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6860410 | GTTCAAGGCCCTCAT[C/T]GGCAAGGGCCACCCT | 8078 |
rs115666159 | snp | G/T | 0.0038981 | 0.0439756 | intron-variant | USP5 | GRCh38.p7 | 12:6855562 | AGGCCTGGGTACATT[G/T]TCTGTTCCATTCTGA | 8078 |
rs115858711 | snp | A/G | 0.0495547 | 0.149404 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | USP5, CDCA3 | GRCh38.p7 | 12:6851832 | AGTTCCTGCTCTTCA[A/G]TAGAAGGCACGCGAA | 8078 |
rs116196909 | snp | A/G | 0.0168055 | 0.0901129 | intron-variant | USP5 | GRCh38.p7 | 12:6860750 | AAGAAAAATACAAGC[A/G]TGTTCTAACACAGTC | 8078 |
rs116418094 | snp | A/G/T | 0.0134541 | 0.0809187 | intron-variant | USP5 | GRCh38.p7 | 12:6863801 | GTGGCCCAATCAGTC[A/G/T]GTCCGTGTACCCACA | 8078 |
rs117876102 | snp | A/G | 0.00456116 | 0.0475371 | synonymous-codon, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6861471 | GTACGAGGAGAAGAA[A/G]CGGCAAGCCGAAGAG | 8078 |
rs137961270 | snp | C/T | 0.000165158 | 0.0090858 | synonymous-codon | USP5 | GRCh38.p7 | 12:6864820 | GGGCCGCTCAGCTGC[C/T]GACTCCATCTCTGAG | 8078 |
rs138130918 | snp | C/G | | | upstream-variant-2KB, utr-variant-3-prime | TPI1, USP5 | GRCh38.p7 | 12:6866420 | TTTGTGCGCGTGGGT[C/G]TAGCTTTGTGCATCC | 8078 |
rs138475962 | snp | C/T | 0.000625834 | 0.0176784 | synonymous-codon, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6860976 | CCGGAGCTCTGAAAA[C/T]CCTAATGAAGTGTTC | 8078 |
rs138526156 | snp | A/G | | | upstream-variant-2KB, intron-variant | TPI1, USP5 | GRCh38.p7 | 12:6865581 | CCCCCTGCCTTTGTA[A/G]ATAAATTTTCACTGG | 8078 |
rs138702168 | snp | C/T | | | intron-variant | USP5 | GRCh38.p7 | 12:6857389 | TTACCTTATCCTATA[C/T]AGGTAGAATCAGAAT | 8078 |
rs138839223 | snp | C/G/T | 0.000346152 | 0.0131514 | synonymous-codon, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6860175 | GGGCCATGGCCTTCT[C/G/T]TCCGGGGAGTATTCC | 8078 |
rs138876608 | snp | A/G | 0.00011536 | 0.00759387 | upstream-variant-2KB, intron-variant | USP5, CDCA3 | GRCh38.p7 | 12:6850454 | ATCAGCATTCCCTGG[A/G]CCCAACGCTTACCTC | 8078 |
rs138879907 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | USP5, CDCA3 | GRCh38.p7 | 12:6851866 | ACTCTAAGGGTCCCG[A/G]AGCCGGAGCAGCTGC | 8078 |
rs139017031 | snp | A/C/G/T | 6.59355e-05 | 0.00574146 | synonymous-codon, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6858510 | GTCAGGTGTGCCACT[A/C/G/T]AAGCCCCTGTTTGGG | 8078 |
rs139290006 | snp | C/T | 8.60519e-05 | 0.00655885 | intron-variant | USP5 | GRCh38.p7 | 12:6863411 | TGCCTGTCTCTCTCC[C/T]GTGCTGATGGGGGCC | 8078 |
rs139322893 | snp | C/T | 6.60742e-05 | 0.00574741 | synonymous-codon, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6858550 | ACAGGCATCCGGAAC[C/T]TGGGTAACAGCTGCT | 8078 |
rs139334200 | snp | C/T | 0.000362337 | 0.013455 | synonymous-codon, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6856063 | GAAGTTTGAATTAGA[C/T]GAGGATGTGAAGATT | 8078 |
rs139353870 | snp | A/G | | | intron-variant | USP5 | GRCh38.p7 | 12:6859786 | GTCTCCTGAGTAGCT[A/G]GGACTACAGGCACAT | 8078 |
rs139483668 | snp | C/T | 5.02365e-05 | 0.00501156 | missense, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6863895 | CCTATGGACGCCTGC[C/T]GCAAAGCTGTCTACT | 8078 |
rs139586443 | snp | C/T | | | upstream-variant-2KB, splice-donor-variant | TPI1, USP5 | GRCh38.p7 | 12:6866634 | GTACAACGGCTAAAT[C/T]GTGTCCTGTTTGATA | 8078 |
rs139833814 | snp | C/G | | | intron-variant | USP5 | GRCh38.p7 | 12:6862653 | CTCAAAGTTTCCTCT[C/G]AAAGAGGAAAAAAAA | 8078 |
rs139973208 | snp | C/T | | | intron-variant | USP5 | GRCh38.p7 | 12:6859206 | ACAGGTTCTGTCCAA[C/T]AGAACGTGAACTGCA | 8078 |
rs139976903 | snp | C/G | 9.95685e-05 | 0.00705509 | synonymous-codon, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6855508 | AGTCTACTTGCACCT[C/G]CGGCGGACCCGGCGC | 8078 |
rs140178036 | in-del | -/C | | | upstream-variant-2KB, intron-variant | USP5, CDCA3 | GRCh38.p7 | 12:6850272 | ATCTGACCACCCCGG[-/C]CTTCCAACGTGCTGG | 8078 |
rs140425478 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP5, CDCA3 | GRCh38.p7 | 12:6852904 | AGCAATGGCCGCAGC[C/T]CCCACCCTTCCCCCC | 8078 |
rs140615476 | snp | C/T | 4.968e-05 | 0.00498373 | intron-variant | USP5 | GRCh38.p7 | 12:6855715 | ACTTGTTCCTTCGCT[C/T]GTGCTCATTGCTGAT | 8078 |
rs140761461 | snp | A/G | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6856411 | CTAAGCATGCCTTCA[A/G]CCTCAAGCAGTTGGA | 8078 |
rs140810255 | snp | A/G | | | intron-variant | USP5 | GRCh38.p7 | 12:6854960 | CCTCTCCCATGAAGG[A/G]ACCCTTTTTCCCTTT | 8078 |
rs140918109 | snp | C/T | | | intron-variant | USP5 | GRCh38.p7 | 12:6859944 | ACAGGCGTGAGCCAC[C/T]GTGCACGGCCACCAC | 8078 |
rs141113721 | snp | C/G | 1.64923e-05 | 0.00287156 | synonymous-codon, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6857687 | CCTGGCTGAGCACCT[C/G]TCCCACTTCGGCATC | 8078 |
rs141573257 | snp | C/T | | | upstream-variant-2KB, intron-variant | TPI1, USP5 | GRCh38.p7 | 12:6865640 | TTGTGCCTGTTTTCA[C/T]GCTGCGGCAGGAAAG | 8078 |
rs141603518 | snp | A/G | | | intron-variant | USP5 | GRCh38.p7 | 12:6861305 | TGCATGGAAACAGGC[A/G]AGATATATTGGACAT | 8078 |
rs141719928 | snp | A/C | | | upstream-variant-2KB, utr-variant-3-prime | TPI1, USP5 | GRCh38.p7 | 12:6866599 | TCTGGAAAATGCCAA[A/C]ATACACGATGTGAAT | 8078 |
rs141770469 | snp | A/G | 1.6473e-05 | 0.00286988 | missense, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6859492 | GATAAGCTGGAGAAG[A/G]TCTTCCAGAATGCCC | 8078 |
rs141809797 | snp | A/G | 0.000264738 | 0.0115021 | synonymous-codon, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6864126 | CGACCCCCCTCCTGA[A/G]GACTGTGTGACCACC | 8078 |
rs141869825 | snp | A/G | 0.00039572 | 0.0140607 | synonymous-codon, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6860208 | GCCAGTACCGGAGTC[A/G]GGCGATGGGGAGCGG | 8078 |
rs141872219 | snp | A/C/T | 8.2364e-05 | 0.00641686 | synonymous-codon, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6859521 | CCCGACGGACCCTAC[A/C/T]CAGGATTTCAGCACC | 8078 |
rs141933928 | snp | A/G | 0.00125229 | 0.0249915 | synonymous-codon, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6860199 | GTATTCCAAGCCAGT[A/G]CCGGAGTCGGGCGAT | 8078 |
rs142003968 | snp | A/G | 0.000760699 | 0.0194877 | upstream-variant-2KB, utr-variant-5-prime, intron-variant, nc-transcript-variant | USP5, CDCA3 | GRCh38.p7 | 12:6851000 | CCAGCCCGGGACGAG[A/G]AGGGAATGCCTGTGA | 8078 |
rs142133780 | snp | C/T | 1.65258e-05 | 0.00287448 | synonymous-codon, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6863227 | CTCGACATCTCCCAG[C/T]TGAGGGGCACAGGGC | 8078 |
rs142252474 | snp | A/G | | | intron-variant | USP5 | GRCh38.p7 | 12:6863773 | GTCCTGGGGGAGGGA[A/G]GAGGAGCAAACAGTG | 8078 |
rs142385593 | snp | A/G | 0.000623405 | 0.0176441 | upstream-variant-2KB, utr-variant-3-prime | TPI1, USP5 | GRCh38.p7 | 12:6866128 | AAGACCACCTGGCAT[A/G]AGGGAGAGGGGCTGA | 8078 |
rs142748785 | snp | A/G | | | intron-variant | USP5 | GRCh38.p7 | 12:6857476 | AGAAGGGCCATGACC[A/G]CACTCATATTACTCA | 8078 |
rs143204334 | snp | C/T | 4.94295e-05 | 0.00497115 | upstream-variant-2KB, missense, utr-variant-5-prime, nc-transcript-variant | USP5, CDCA3 | GRCh38.p7 | 12:6850563 | CCTCCAGTTGCTCCC[C/T]TGCTGGTAGGCCTGG | 8078 |
rs143249320 | snp | C/T | 0.00710715 | 0.0591867 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | USP5, CDCA3 | GRCh38.p7 | 12:6852233 | ACCGACGATCCGGGT[C/T]CCTAAGGCTGGAGAC | 8078 |
rs143332941 | snp | A/G | 0.00126781 | 0.0251456 | synonymous-codon, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6859470 | TCCCTTGACTTTTAG[A/G]TATGTGGATAAGCTG | 8078 |
rs143386381 | snp | A/G | 0.00209039 | 0.0322618 | intron-variant | USP5 | GRCh38.p7 | 12:6856268 | GGCATGTGGGGCAGG[A/G]GGTTGGGTATTGCCT | 8078 |
rs143399294 | snp | A/G | | | intron-variant | USP5 | GRCh38.p7 | 12:6855155 | TTGAATGGCGACGAT[A/G]AGCTGGTGTTCCTCA | 8078 |
rs143479000 | snp | A/G | 0.00120628 | 0.0245293 | intron-variant | USP5 | GRCh38.p7 | 12:6861138 | GCAAGGCCGTGGCAC[A/G]GTGGGAGGCTAAGGT | 8078 |
rs143750403 | snp | A/G | 0.000329413 | 0.0128296 | synonymous-codon, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6859509 | CTTCCAGAATGCCCC[A/G]ACGGACCCTACCCAG | 8078 |
rs143986399 | snp | C/T | 0.000988012 | 0.0222043 | synonymous-codon, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6861073 | GACTACATCATGCAG[C/T]TGCCTGTGCCCATGG | 8078 |
rs144110837 | snp | C/T | | | intron-variant | USP5 | GRCh38.p7 | 12:6858839 | GCCTGGGCAACATAG[C/T]GAGACCCTGTCTTCT | 8078 |
rs144155137 | snp | G/T | | | intron-variant, upstream-variant-2KB | USP5, CDCA3 | GRCh38.p7 | 12:6853360 | TCATCACTGTGATTT[G/T]TGGTTTGCTTGGTTT | 8078 |
rs144201804 | snp | A/G | 1.65154e-05 | 0.00287358 | synonymous-codon, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6855490 | CAATAAGACCGGCCA[A/G]CGAGTCTACTTGCAC | 8078 |
rs144448240 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP5, CDCA3 | GRCh38.p7 | 12:6853891 | GAGCAATCTATGGGA[C/T]CAAGAACTACCTTAG | 8078 |
rs145045370 | snp | A/G | | | upstream-variant-2KB, intron-variant | USP5, CDCA3 | GRCh38.p7 | 12:6850368 | CCGAAGCAGGAGGAT[A/G]GAGGCCCCTTTAAGG | 8078 |
rs145192789 | snp | C/T | | | intron-variant | USP5 | GRCh38.p7 | 12:6855910 | AAAGAGTGGGCCTGA[C/T]TGATGGCCCTAGAAC | 8078 |
rs145233386 | snp | G/T | | | intron-variant | USP5 | GRCh38.p7 | 12:6863646 | AAACAGGGCCCATTC[G/T]GTGAGAATGGGCAGG | 8078 |
rs145375496 | snp | A/G/T | 0.000305175 | 0.012349 | synonymous-codon, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6864183 | CCAGGCCTTGAAAGC[A/G/T]CTGCGGGCCACGGTA | 8078 |
rs145639640 | snp | C/T | 8.25048e-05 | 0.00642228 | upstream-variant-2KB, intron-variant | USP5, CDCA3 | GRCh38.p7 | 12:6850647 | TGACTCTTCTCTCCT[C/T]TCCTCCCCATATTCC | 8078 |
rs145733981 | snp | C/T | 0.000726636 | 0.019047 | synonymous-codon, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6855778 | GGACCCTGCTACAGG[C/T]ACTGGAGACCCACCC | 8078 |
rs145842344 | snp | A/C/T | 6.5945e-05 | 0.00574184 | intron-variant | USP5 | GRCh38.p7 | 12:6860140 | AAATGTTTTCTTGGA[A/C/T]ATTAATGCAGGGCCA | 8078 |
rs146230726 | snp | A/G | 0.000625079 | 0.0176677 | synonymous-codon, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6863933 | CAACAGCGGGGCTGA[A/G]GCCGCCATGAACTGG | 8078 |
rs146260415 | snp | A/G | | | upstream-variant-2KB, utr-variant-3-prime | TPI1, USP5 | GRCh38.p7 | 12:6866337 | GCTTCCCCTGCCCCC[A/G]GAATCCACAGTGCTC | 8078 |
rs146281303 | snp | A/G | 0.00112133 | 0.0236518 | synonymous-codon, intron-variant, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6863373 | TCACTTCTCCTCTCC[A/G]ACATGTTAGTGACTC | 8078 |
rs146283615 | snp | A/G | 0.000774791 | 0.0196671 | missense, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6860209 | CCAGTACCGGAGTCG[A/G]GCGATGGGGAGCGGG | 8078 |
rs146802822 | snp | C/T | | | intron-variant | USP5 | GRCh38.p7 | 12:6855328 | AGCAGTTTCTGACTC[C/T]AGGTTTTGGTTTCCT | 8078 |
rs146916229 | snp | C/T | 0.000560704 | 0.0167343 | synonymous-codon, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6857696 | GCACCTGTCCCACTT[C/T]GGCATCGACATGCTG | 8078 |
rs147089551 | snp | C/G | | | intron-variant | USP5 | GRCh38.p7 | 12:6857254 | TGAGCTATGATTGCA[C/G]CACTGGACTCCAGCC | 8078 |
rs147157708 | snp | C/G | | | intron-variant, upstream-variant-2KB | USP5, CDCA3 | GRCh38.p7 | 12:6852722 | CCGGGGTTGGAGTTG[C/G]GGGGTGGGGACCGCA | 8078 |
rs147989718 | snp | C/T | | | synonymous-codon, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6863220 | AGAGGAGCTCGACAT[C/T]TCCCAGTTGAGGGGC | 8078 |
rs148012926 | snp | A/G | | | intron-variant | USP5 | GRCh38.p7 | 12:6861295 | TTAGCAGAGCTGCAT[A/G]GAAACAGGCGAGATA | 8078 |
rs148155861 | snp | C/T | | | upstream-variant-2KB, intron-variant | USP5, CDCA3 | GRCh38.p7 | 12:6850702 | GATATCCAGCCTACC[C/T]CACACAGATTGAGAT | 8078 |
rs148381090 | snp | A/G | | | intron-variant | USP5 | GRCh38.p7 | 12:6856983 | ATACATGAATGCATT[A/G]TCTTGATAAGAAAGG | 8078 |
rs148414360 | snp | A/G | | | intron-variant | USP5 | GRCh38.p7 | 12:6854179 | ATGTGTGTTCTAGCT[A/G]TCTCAGCAAGTGTTG | 8078 |
rs148640344 | snp | A/C | 3.2962e-05 | 0.00405954 | missense, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6862536 | GTTCACCTTCGGCTT[A/C]GACTGGGTGCCCAAG | 8078 |
rs148745027 | snp | C/G | | | intron-variant | USP5 | GRCh38.p7 | 12:6863729 | CATGGGAGAAAAATG[C/G]ATGGAATGGGTGATT | 8078 |
rs149056495 | snp | C/T | | | intron-variant | USP5 | GRCh38.p7 | 12:6865051 | TGGCCCAGTACCTGC[C/T]TCACATTCCCTGAAA | 8078 |
rs149145992 | snp | C/T | 0.0082025 | 0.0635135 | synonymous-codon, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6856096 | CATTTTGCCAGATTA[C/T]CTGGAGATTGCCCGG | 8078 |
rs149461149 | snp | C/T | | | intron-variant | USP5 | GRCh38.p7 | 12:6858712 | CACCTCTGTGTTTGA[C/T]TCTAGTCTTAGAGTA | 8078 |
rs149515919 | snp | A/C | 0.000149456 | 0.00864324 | missense, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6860480 | TTCCTTCACCTTATC[A/C]ACATGGTGGAGGTAA | 8078 |
rs149569083 | snp | C/T | 3.29609e-05 | 0.00405948 | missense, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6855435 | ACATCTGTATGAACA[C/T]GTTTCTGGGCTTTGG | 8078 |
rs149667187 | snp | C/T | 9.8868e-05 | 0.00703024 | synonymous-codon, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6856818 | TGGGGGCAACAACCA[C/T]GCTGTGGAGCACTAC | 8078 |
rs149791950 | snp | C/G | | | upstream-variant-2KB, intron-variant | TPI1, USP5 | GRCh38.p7 | 12:6867050 | TCCCGCAAGTTTTCA[C/G]TCAGGTAGACTCCCT | 8078 |
rs150199223 | snp | A/G | | | intron-variant | USP5 | GRCh38.p7 | 12:6859945 | CAGGCGTGAGCCACC[A/G]TGCACGGCCACCACT | 8078 |
rs150459329 | snp | C/T | 0.0025901 | 0.0358935 | synonymous-codon, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6864175 | TCCCGGGACCAGGCC[C/T]TGAAAGCGCTGCGGG | 8078 |
rs150511748 | snp | C/T | | | intron-variant | USP5 | GRCh38.p7 | 12:6862288 | AGCCTTCCTTCTGGC[C/T]TCTACTGCTCCTCGT | 8078 |
rs150566092 | snp | A/G | | | upstream-variant-2KB, utr-variant-3-prime | TPI1, USP5 | GRCh38.p7 | 12:6866609 | GCCAAAATACACGAT[A/G]TGAATAAAAGTACAA | 8078 |
rs150704956 | snp | C/G | | | upstream-variant-2KB, intron-variant | USP5, CDCA3 | GRCh38.p7 | 12:6851030 | AGAAGTGACTCAGGT[C/G]TCAGCCCTTATCTCT | 8078 |
rs150858074 | snp | A/G | 0.00841721 | 0.0643254 | upstream-variant-2KB, missense, utr-variant-5-prime, nc-transcript-variant | USP5, CDCA3 | GRCh38.p7 | 12:6850587 | GGCCTGGCTGTGGAG[A/G]GCTCTCCACCTGTCA | 8078 |
rs150961616 | snp | A/G | 0.000279999 | 0.0118288 | synonymous-codon, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6856099 | TTTGCCAGATTACCT[A/G]GAGATTGCCCGGGAT | 8078 |
rs151018445 | snp | A/G | | | intron-variant | USP5 | GRCh38.p7 | 12:6854283 | GGAGGGGAGGCAGAG[A/G]AGAGAGGGTGGTGGC | 8078 |
rs151164847 | in-del | -/G | | | intron-variant, upstream-variant-2KB | USP5, CDCA3 | GRCh38.p7 | 12:6853064 | CACCTCCCACACCAT[-/G]CTTCACGTTTTGCAG | 8078 |
rs180780091 | snp | G/T | | | upstream-variant-2KB, intron-variant | TPI1, USP5 | GRCh38.p7 | 12:6865617 | GGACACACTTGTTTA[G/T]GTGTTGTTTGTGCCT | 8078 |
rs181013107 | snp | C/T | 0.000741162 | 0.0192362 | intron-variant | USP5 | GRCh38.p7 | 12:6859573 | TATGTAGGAAAGCTG[C/T]TGACAGTCATGGCCG | 8078 |
rs181300669 | snp | A/G | | | intron-variant | USP5 | GRCh38.p7 | 12:6859951 | TGAGCCACCGTGCAC[A/G]GCCACCACTGGCCTA | 8078 |
rs181654492 | snp | A/C | | | intron-variant, upstream-variant-2KB | USP5, CDCA3 | GRCh38.p7 | 12:6853996 | TCTGTTGTTGCTCAA[A/C]GCCTTGGATCTGAGG | 8078 |
rs181697742 | snp | A/G | | | intron-variant | USP5 | GRCh38.p7 | 12:6859305 | ACATAGCTGAGAAGG[A/G]GAGAACAGGCAGGTT | 8078 |
rs181922891 | snp | A/G | 8.33966e-05 | 0.00645688 | missense, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6864164 | CCATGGGCTTCTCCC[A/G]GGACCAGGCCTTGAA | 8078 |
rs182141134 | snp | C/G | | | intron-variant | USP5 | GRCh38.p7 | 12:6854733 | ACTGCACTCCAGCCT[C/G]GGTGACAGAGTGCAG | 8078 |
rs182182969 | snp | C/T | 3.29478e-05 | 0.00405867 | synonymous-codon, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6856042 | CGGATTTGACCTTAG[C/T]GAGGAGAAGTTTGAA | 8078 |
rs182729366 | snp | C/T | | | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | USP5, CDCA3 | GRCh38.p7 | 12:6851706 | CAACCCCCTCAAGCT[C/T]CGCCTCACTGGATAC | 8078 |
rs183012599 | snp | C/G | | | upstream-variant-2KB, intron-variant | USP5, CDCA3 | GRCh38.p7 | 12:6851094 | TCTTCCCAGTTTCCA[C/G]TGAAGAAACTTCCTG | 8078 |
rs183356425 | snp | G/T | | | intron-variant, upstream-variant-2KB | USP5, CDCA3 | GRCh38.p7 | 12:6852474 | TGACTACCGTCCCCG[G/T]AAGCCGCCGCGCTCA | 8078 |
rs183579487 | snp | C/T | 1.65135e-05 | 0.00287341 | missense, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6858544 | GGCTACACAGGCATC[C/T]GGAACCTGGGTAACA | 8078 |
rs183584582 | snp | C/T | 1.65061e-05 | 0.00287277 | intron-variant | USP5 | GRCh38.p7 | 12:6860107 | GGGGACACACAGGGT[C/T]GTTAGTTGACTGAAG | 8078 |
rs183840287 | snp | A/G/T | 0.00138737 | 0.026302 | intron-variant | USP5 | GRCh38.p7 | 12:6856669 | CTCCCTCAAATCCCC[A/G/T]ACCCACATTTCTGCT | 8078 |
rs183956827 | snp | C/T | | | intron-variant | USP5 | GRCh38.p7 | 12:6857346 | TACTCCCCACTCAAA[C/T]CCTCATCCCTTTCCT | 8078 |
rs184076065 | snp | C/G | | | intron-variant, upstream-variant-2KB | USP5, CDCA3 | GRCh38.p7 | 12:6853811 | AGCTTAGTTGACCTC[C/G]CCGGTGAGAAATGCT | 8078 |
rs184495101 | snp | A/C | 0.000118212 | 0.00768714 | intron-variant | USP5 | GRCh38.p7 | 12:6863388 | GACATGTTAGTGACT[A/C]TTCTTCCTGCCTGTC | 8078 |
rs184696948 | snp | C/T | | | intron-variant | USP5 | GRCh38.p7 | 12:6858965 | AAACCCCACTGATAG[C/T]GCAGAGTGCCAAGTC | 8078 |
rs184746814 | snp | C/T | | | intron-variant, downstream-variant-500B | USP5 | GRCh38.p7 | 12:6864570 | GGTGGGCGTCTGTAG[C/T]CCCAGCTACTTGGGA | 8078 |
rs184861396 | snp | A/C/G | | | intron-variant | USP5 | GRCh38.p7 | 12:6862641 | AAACTAGTGTTTCTC[A/C/G]AAGTTTCCTCTGAAA | 8078 |
rs185292868 | snp | A/T | | | intron-variant | USP5 | GRCh38.p7 | 12:6859631 | GGGGGCACAGCACTT[A/T]AACCCCTGGCCTTTT | 8078 |
rs185487543 | snp | G/T | | | intron-variant, upstream-variant-2KB | USP5, CDCA3 | GRCh38.p7 | 12:6853432 | TGAAGTCTGGCTTTG[G/T]CAGAGGTAAAAGAGC | 8078 |
rs185830650 | snp | A/G | 0.00697962 | 0.0586608 | missense, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6856338 | GCCCTACTGTCGGCC[A/G]ACTCAGCCTCCCGCA | 8078 |
rs185945256 | snp | A/G | | | upstream-variant-2KB, intron-variant | USP5, CDCA3 | GRCh38.p7 | 12:6851190 | CCTGCTGAGCCCTCT[A/G]ACTTATTTATTAAAT | 8078 |
rs186378241 | snp | C/T | | | intron-variant | USP5 | GRCh38.p7 | 12:6859953 | AGCCACCGTGCACGG[C/T]CACCACTGGCCTATT | 8078 |
rs186483580 | snp | A/C | | | upstream-variant-2KB, intron-variant | TPI1, USP5 | GRCh38.p7 | 12:6865780 | GGTGGTTGTAAAGGT[A/C]CTGGAGGATCTGAAG | 8078 |
rs186668681 | snp | A/G | | | intron-variant | USP5 | GRCh38.p7 | 12:6862054 | TTTGCTGCTCCTGCC[A/G]GTGAAACAGCTCTTC | 8078 |
rs186722917 | snp | A/G | | | intron-variant | USP5 | GRCh38.p7 | 12:6854627 | TCTAGGCATGGTGGC[A/G]TGTGCCTGTAGTCCC | 8078 |
rs187058578 | snp | C/G | 0.00167708 | 0.028909 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | USP5, CDCA3 | GRCh38.p7 | 12:6852175 | GAGAAGCTGCTGCCG[C/G]TGTCATGGCGGAGCT | 8078 |
rs187242191 | snp | G/T | | | intron-variant | USP5 | GRCh38.p7 | 12:6855063 | ATAGAGGTGAAGGAA[G/T]TCCTCTGTGATTGAT | 8078 |
rs187318712 | snp | C/T | | | intron-variant | USP5 | GRCh38.p7 | 12:6859337 | CTGGAGAGAAGCGAC[C/T]CCAAGGTTCACCCAC | 8078 |
rs187591628 | snp | C/T | 0.00126817 | 0.0251491 | upstream-variant-2KB, intron-variant | USP5, CDCA3 | GRCh38.p7 | 12:6850460 | ATTCCCTGGGCCCAA[C/T]GCTTACCTCCACTGC | 8078 |
rs187648383 | snp | C/T | | | intron-variant | USP5 | GRCh38.p7 | 12:6857471 | GCCCCAGAAGGGCCA[C/T]GACCGCACTCATATT | 8078 |
rs188171672 | snp | G/T | | | intron-variant | USP5 | GRCh38.p7 | 12:6862700 | AAAATTTATCTAGTT[G/T]GAAAGCACTAACTAA | 8078 |
rs188377905 | snp | C/T | 0.000823285 | 0.0202723 | intron-variant | USP5 | GRCh38.p7 | 12:6856906 | GGTACAGCCTCCCCT[C/T]CTCCAGCCACTCTCA | 8078 |
rs188467892 | snp | G/T | | | intron-variant, upstream-variant-2KB | USP5, CDCA3 | GRCh38.p7 | 12:6853990 | AGGATGTCTGTTGTT[G/T]CTCAAAGCCTTGGAT | 8078 |
rs188711515 | snp | C/T | | | intron-variant | USP5 | GRCh38.p7 | 12:6858773 | CCCGTAATCCCAGTA[C/T]TTCGGGAGGCCAAGA | 8078 |
rs189212228 | snp | A/C | | | intron-variant, upstream-variant-2KB | USP5, CDCA3 | GRCh38.p7 | 12:6852909 | TGGCCGCAGCCCCCA[A/C]CCTTCCCCCCGCCCC | 8078 |
rs189219141 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP5, CDCA3 | GRCh38.p7 | 12:6853557 | ATTCTTCCCAGGAGG[A/G]AAAGGTTTTTCTTAA | 8078 |
rs189627934 | snp | C/T | 0.00266067 | 0.0363766 | intron-variant | USP5 | GRCh38.p7 | 12:6863800 | AGTGGCCCAATCAGT[C/T]GGTCCGTGTACCCAC | 8078 |
rs189651154 | snp | A/G | | | intron-variant | USP5 | GRCh38.p7 | 12:6859677 | TTTGTTTTTTGAGAC[A/G]GAGTCTTGTTCTGTT | 8078 |
rs189685715 | snp | C/T | | | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | USP5, CDCA3 | GRCh38.p7 | 12:6851317 | CCCCCTGCCCTGACC[C/T]TATTGGCTGAGCCGA | 8078 |
rs189935596 | snp | C/T | | | intron-variant | USP5 | GRCh38.p7 | 12:6855609 | GTTTCTTTTTTTCAC[C/T]TACTTTTGTGTCATT | 8078 |
rs190047278 | snp | C/T | | | intron-variant | USP5 | GRCh38.p7 | 12:6859274 | TCCTCTGCCGCCGAG[C/T]GTGCTTGCACATTGG | 8078 |
rs190200818 | snp | A/G | 0.000215255 | 0.0103721 | synonymous-codon, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6856391 | TGGGGAAGTACGGCA[A/G]GTGTCTAAGCATGCC | 8078 |
rs191155199 | snp | A/C | | | intron-variant, upstream-variant-2KB | USP5, CDCA3 | GRCh38.p7 | 12:6853646 | CTCTCTCCTTAGTAA[A/C]TGCTTTGAATAATCC | 8078 |
rs191370929 | snp | A/G | | | upstream-variant-2KB, utr-variant-3-prime | TPI1, USP5 | GRCh38.p7 | 12:6866278 | GGGATGGAGCAGGAC[A/G]GGGACGGGAGGGGCC | 8078 |
rs191401680 | snp | C/T | | | intron-variant | USP5 | GRCh38.p7 | 12:6858216 | TCATTCAAGCAGAGG[C/T]CCTGATGACTAACGG | 8078 |
rs191689746 | snp | C/T | | | intron-variant | USP5 | GRCh38.p7 | 12:6860045 | ATCTAAGGTTTTTCA[C/T]GTTGTTGAGAGTTAG | 8078 |
rs191917652 | snp | C/G | | | upstream-variant-2KB, intron-variant | USP5, CDCA3 | GRCh38.p7 | 12:6850685 | AATTGCCAAGGCCCT[C/G]AGATATCCAGCCTAC | 8078 |
rs192268986 | snp | C/T | 0.000498549 | 0.0157806 | missense, upstream-variant-2KB, nc-transcript-variant | USP5, CDCA3 | GRCh38.p7 | 12:6852241 | TCCGGGTCCCTAAGG[C/T]TGGAGACCGGGTCCA | 8078 |
rs192561839 | snp | G/T | | | intron-variant | USP5 | GRCh38.p7 | 12:6862156 | TGCTATGTTGCCCAG[G/T]TTGGTCTCTTAACTC | 8078 |
rs192970712 | snp | A/G | | | intron-variant | USP5 | GRCh38.p7 | 12:6863112 | GTTCTGACATAGGGG[A/G]CAGGGGATTGAGGTT | 8078 |
rs193025352 | snp | A/C | | | intron-variant | USP5 | GRCh38.p7 | 12:6857004 | ATAAGAAAGGAAAGT[A/C]GTCAGGTGCGGTGGC | 8078 |
rs193089322 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP5, CDCA3 | GRCh38.p7 | 12:6853019 | GCCTCTTTCCCATCC[C/T]GCTCCCACTCTTGGC | 8078 |
rs199632125 | snp | G/T | 3.34269e-05 | 0.00408807 | missense, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6861511 | GCACTGCCAGAACTG[G/T]TTCGGGCCCAGGTGC | 8078 |
rs199642135 | snp | A/G | 0.00254566 | 0.0355858 | intron-variant | USP5 | GRCh38.p7 | 12:6856273 | GTGGGGCAGGGGGTT[A/G]GGTATTGCCTCTGAC | 8078 |
rs199679807 | snp | C/T | 0.00301481 | 0.0387081 | intron-variant | USP5 | GRCh38.p7 | 12:6856908 | TACAGCCTCCCCTCC[C/T]CCAGCCACTCTCATG | 8078 |
rs199918732 | snp | C/T | 0.000135368 | 0.00822593 | synonymous-codon, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6863936 | CAGCGGGGCTGAGGC[C/T]GCCATGAACTGGGTC | 8078 |
rs200040016 | snp | C/G | 4.94189e-05 | 0.00497062 | missense, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6859524 | GACGGACCCTACCCA[C/G]GATTTCAGCACCCAG | 8078 |
rs200061658 | snp | C/T | 0.000148301 | 0.00860978 | upstream-variant-2KB, intron-variant | USP5, CDCA3 | GRCh38.p7 | 12:6850600 | AGAGCTCTCCACCTG[C/T]CAAGACCATAGGCTA | 8078 |
rs200147836 | snp | C/T | 8.47192e-05 | 0.00650787 | upstream-variant-2KB, intron-variant | USP5, CDCA3 | GRCh38.p7 | 12:6850808 | TTCAGACATTCTCTG[C/T]CTTTCCCACGCTGGC | 8078 |
rs200151898 | snp | A/G | 0.00417947 | 0.0455222 | missense, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6856714 | TGGGTTAGTGGCTGG[A/G]AGTGCTCCAAGTGTG | 8078 |
rs200338885 | snp | C/T | 1.69304e-05 | 0.00290945 | intron-variant | USP5 | GRCh38.p7 | 12:6864718 | TGCTTCCTTCCTCTC[C/T]AAGAACAATAGTTTA | 8078 |
rs200353491 | snp | A/G | 0.000115623 | 0.00760251 | missense, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6860411 | TTCAAGGCCCTCATC[A/G]GCAAGGGCCACCCTG | 8078 |
rs200472768 | snp | C/T | 4.96734e-05 | 0.0049834 | missense, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6856386 | TGGGATGGGGAAGTA[C/T]GGCAGGTGTCTAAGC | 8078 |
rs200475983 | snp | A/G | 0.000132107 | 0.00812626 | missense, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6855795 | CTGGAGACCCACCCC[A/G]GAAGAAGCCCACGCG | 8078 |
rs200493713 | snp | C/T | 8.24518e-05 | 0.00642021 | synonymous-codon | USP5 | GRCh38.p7 | 12:6865222 | CATGTGTGGTCACTA[C/T]GTCTGCCACATCAAG | 8078 |
rs200553357 | snp | G/T | 0.00110624 | 0.0234925 | intron-variant | USP5 | GRCh38.p7 | 12:6856180 | TATGCTACCCAAGAT[G/T]CTAGAGCAAGATGGG | 8078 |
rs200559409 | snp | A/G | 1.82015e-05 | 0.00301669 | intron-variant | USP5 | GRCh38.p7 | 12:6861403 | AGGAGGCAAAGAAGC[A/G]GCACCCTCCGAAGGA | 8078 |
rs200560402 | snp | A/G | 0.00519503 | 0.0507003 | upstream-variant-2KB, intron-variant | USP5, CDCA3 | GRCh38.p7 | 12:6850620 | ACCATAGGCTAGAAC[A/G]AGTCTGGGCCCTGAC | 8078 |
rs200589400 | snp | C/T | | | upstream-variant-2KB, missense, utr-variant-5-prime, nc-transcript-variant | USP5, CDCA3 | GRCh38.p7 | 12:6850517 | CCAAGAGTAGGAGAG[C/T]GGGGATCTGAGTCCT | 8078 |
rs200608693 | snp | A/T | 1.68698e-05 | 0.00290424 | synonymous-codon, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6863876 | GCTGGTGGAGATGGG[A/T]TTCCCTATGGACGCC | 8078 |
rs200664735 | snp | A/G | 1.64933e-05 | 0.00287165 | missense, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6857631 | CCTCCTGCTCTAGAC[A/G]TGTACTCATATGATG | 8078 |
rs200723728 | snp | A/G | 0.000873369 | 0.0208787 | missense, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6856835 | CTGTGGAGCACTACC[A/G]AGAGACAGGCTACCC | 8078 |
rs200867324 | in-del | -/T | | | intron-variant | USP5 | GRCh38.p7 | 12:6862083 | TCCTCTCTGTGTGGG[-/T]TTTTTTTTTTTTTCT | 8078 |
rs200956770 | snp | C/G/T | 1.99555e-05 | 0.00315869 | missense, upstream-variant-2KB, nc-transcript-variant | USP5, CDCA3 | GRCh38.p7 | 12:6852240 | ATCCGGGTCCCTAAG[C/G/T]CTGGAGACCGGGTCC | 8078 |
rs201018774 | snp | A/G | 6.63724e-05 | 0.00576036 | missense, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6855513 | ACTTGCACCTCCGGC[A/G]GACCCGGCGCCCGGT | 8078 |
rs201103093 | snp | G/T | 0.00117564 | 0.0242165 | synonymous-codon | USP5 | GRCh38.p7 | 12:6864862 | GGGACCTAAAGTCCG[G/T]GATGGTCCTGGAAGT | 8078 |
rs201246451 | snp | C/T | 1.64757e-05 | 0.00287012 | synonymous-codon, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6856794 | TGGGCGACGCTACTT[C/T]GATGGCAGTGGGGGC | 8078 |
rs201277720 | snp | C/T | 6.61835e-05 | 0.00575216 | missense, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6864119 | CAGCAGCCGACCCCC[C/T]TCCTGAGGACTGTGT | 8078 |
rs201285357 | snp | C/T | 3.29908e-05 | 0.00406132 | synonymous-codon, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6860211 | AGTACCGGAGTCGGG[C/T]GATGGGGAGCGGGTG | 8078 |
rs201347142 | snp | A/G | 3.30267e-05 | 0.00406353 | intron-variant | USP5 | GRCh38.p7 | 12:6861125 | GGCTGCTCCATCAGC[A/G]AGGCCGTGGCACGGT | 8078 |
rs201361484 | snp | C/G | 5.04851e-05 | 0.00502394 | intron-variant | USP5 | GRCh38.p7 | 12:6856295 | GCCTCTGACCCTCTG[C/G]TTCCCCCAGGTGACC | 8078 |
rs201388651 | in-del | -/CA | | | upstream-variant-2KB, intron-variant | TPI1, USP5 | GRCh38.p7 | 12:6865879 | GATTTGGGGTATGGG[-/CA]GAGAGTGTGGAGAGC | 8078 |
rs201410113 | snp | A/G | | | intron-variant | USP5 | GRCh38.p7 | 12:6855834 | TTGGTGAGCACCGCT[A/G]CAGTCCTATTCTTCT | 8078 |
rs201462995 | in-del | -/A | | | intron-variant | USP5 | GRCh38.p7 | 12:6854760 | CAGTGTCTCTAAAAT[-/A]AAAATTTTTTTTTTT | 8078 |
rs201535039 | snp | A/T | 0.00199802 | 0.0315439 | synonymous-codon, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6856433 | GCAGTTGGACAACCC[A/T]GCTCGAATCCCTCCC | 8078 |
rs201625392 | snp | C/T | 3.62562e-05 | 0.00425756 | intron-variant | USP5 | GRCh38.p7 | 12:6861625 | GCTGTCAAGTAAGTC[C/T]TCTGGTCGGGGCCTG | 8078 |
rs201681376 | snp | C/T | 0.000708314 | 0.0188057 | intron-variant | USP5 | GRCh38.p7 | 12:6859458 | TCCAACTGTCCTTCC[C/T]TTGACTTTTAGGTAT | 8078 |
rs201872573 | snp | C/T | 1.6516e-05 | 0.00287362 | missense, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6855794 | ACTGGAGACCCACCC[C/T]GGAAGAAGCCCACGC | 8078 |
rs201967970 | snp | C/T | 3.34286e-05 | 0.00408818 | synonymous-codon, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6864168 | GGGCTTCTCCCGGGA[C/T]CAGGCCTTGAAAGCG | 8078 |
rs201977667 | snp | C/T | 0.000461148 | 0.0151777 | missense, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6861056 | AGTACACCCAGCGAG[C/T]TGACTACATCATGCA | 8078 |
rs202020864 | snp | C/T | 1.68286e-05 | 0.0029007 | upstream-variant-2KB, intron-variant | USP5, CDCA3 | GRCh38.p7 | 12:6850825 | TTTCCCACGCTGGCC[C/T]AGAGTACCTGGATGG | 8078 |
rs202049140 | snp | A/G | 0.000181631 | 0.00952797 | missense, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6858545 | GCTACACAGGCATCC[A/G]GAACCTGGGTAACAG | 8078 |
rs202082979 | snp | A/G | 0.000115442 | 0.00759656 | missense, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6860212 | GTACCGGAGTCGGGC[A/G]ATGGGGAGCGGGTGC | 8078 |
rs202087351 | snp | A/G | 0.00199792 | 0.0315431 | missense, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6864103 | CCGGGCTCCACAAGC[A/G]CAGCAGCCGACCCCC | 8078 |
rs202095894 | snp | A/C/G | | | intron-variant | USP5 | GRCh38.p7 | 12:6857849 | CCCCAAGATACACAG[A/C/G]CTTCTTTTAAATATC | 8078 |
rs202138409 | snp | G/T | 0.000750494 | 0.0193567 | intron-variant | USP5 | GRCh38.p7 | 12:6860524 | GGCACACCCCCATCT[G/T]CCTGCAATTTACTCG | 8078 |
rs202159400 | snp | C/T | 0.000758625 | 0.0194612 | intron-variant | USP5 | GRCh38.p7 | 12:6862568 | AACTGGGTATGGCTG[C/T]TGGAATGAGGGAGGT | 8078 |
rs202226777 | snp | A/G | 1.65192e-05 | 0.00287391 | synonymous-codon | USP5 | GRCh38.p7 | 12:6864802 | TGCCATGGACATCTC[A/G]GAGGGCCGCTCAGCT | 8078 |
rs367554850 | snp | A/T | | | intron-variant, upstream-variant-2KB | USP5, TPI1 | GRCh38.p7 | 12:6865460 | TAGAGATGGGATCTC[A/T]CTATGTTGCCCAGGC | 8078 |
rs367652776 | snp | C/G | 1.64746e-05 | 0.00287002 | missense, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6856037 | GAAGGCGGATTTGAC[C/G]TTAGCGAGGAGAAGT | 8078 |
rs367656277 | snp | A/G | 1.64776e-05 | 0.00287028 | missense, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6862520 | TCATCCAGATCAAGA[A/G]GTTCACCTTCGGCTT | 8078 |
rs367680498 | snp | A/C | 1.69844e-05 | 0.00291409 | intron-variant | USP5 | GRCh38.p7 | 12:6865119 | GGCCATCACTCAAGC[A/C]TTCCTCTTCTGTTTC | 8078 |
rs367726225 | snp | C/T | 0.000131796 | 0.00811668 | upstream-variant-2KB, missense, nc-transcript-variant | USP5, CDCA3 | GRCh38.p7 | 12:6850485 | CACTGCTGGTCTTCA[C/T]AGGTGTCCGTGCAAT | 8078 |
rs367735890 | snp | C/T | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6863971 | CACACATGGATGATC[C/T]AGGTAGGCTGGGGTG | 8078 |
rs367843258 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | USP5, CDCA3 | GRCh38.p7 | 12:6851876 | TCCCGGAGCCGGAGC[A/G]GCTGCGGAGCCGCAG | 8078 |
rs367936917 | snp | A/G | 0.00016494 | 0.00907981 | synonymous-codon, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6856851 | AGAGACAGGCTACCC[A/G]TTAGCTGTCAAGCTG | 8078 |
rs367942459 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | USP5 | GRCh38.p7 | 12:6855542 | GTAGGAGCAGGGCTG[A/G]GGCAAGGCCTGGGTA | 8078 |
rs367977966 | snp | C/T | 3.35954e-05 | 0.00409836 | upstream-variant-2KB, missense, intron-variant, nc-transcript-variant | USP5, CDCA3 | GRCh38.p7 | 12:6850838 | CCCAGAGTACCTGGA[C/T]GGGAGTGCGCAGGAT | 8078 |
rs368011648 | snp | A/C/T | 0.000295671 | 0.0121552 | intron-variant, upstream-variant-2KB | USP5, CDCA3 | GRCh38.p7 | 12:6852296 | CGACACGCCGGTAAG[A/C/T]CCATTCCCCACGCCC | 8078 |
rs368052685 | snp | A/G | | | intron-variant | USP5 | GRCh38.p7 | 12:6857429 | TTCCAACCCTCACCC[A/G]GTTTCATCTGTCTTC | 8078 |
rs368270613 | snp | C/T | | | upstream-variant-2KB, intron-variant | USP5, CDCA3 | GRCh38.p7 | 12:6850682 | AGGAATTGCCAAGGC[C/T]CTCAGATATCCAGCC | 8078 |
rs368371423 | snp | C/T | 0.000307953 | 0.0124049 | synonymous-codon, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6861459 | GGAGCTTCTGGAGTA[C/T]GAGGAGAAGAAGCGG | 8078 |
rs368387512 | snp | G/T | 0.000153988 | 0.00877328 | intron-variant | USP5 | GRCh38.p7 | 12:6858399 | TGAGTTTCTCACTCA[G/T]TCTGAAGTGCCCCTT | 8078 |
rs368437920 | snp | C/T | 0.000181703 | 0.00952986 | upstream-variant-2KB, intron-variant | TPI1, USP5 | GRCh38.p7 | 12:6865967 | TTCATCCTTTTCTGT[C/T]TTCCCCACTTCCCCA | 8078 |
rs368471644 | snp | A/G | 0.000132231 | 0.00813008 | intron-variant | USP5 | GRCh38.p7 | 12:6855856 | TATTCTTCTCCCTGA[A/G]CTGGTCTTTCTGGCT | 8078 |
rs368551360 | snp | A/G | 1.75339e-05 | 0.00296085 | intron-variant | USP5 | GRCh38.p7 | 12:6856474 | TGGCCCCTCTGCCTC[A/G]GGCACCACCCCCAGA | 8078 |
rs368767886 | snp | C/T | | | intron-variant | USP5 | GRCh38.p7 | 12:6860749 | AAAGAAAAATACAAG[C/T]GTGTTCTAACACAGT | 8078 |
rs368924849 | snp | C/T | 0.00019023 | 0.00975083 | intron-variant | USP5 | GRCh38.p7 | 12:6858633 | GTGAGTAGTGCCCTC[C/T]CCTTCCCCAGGCCCC | 8078 |
rs369075638 | snp | A/C | 3.30393e-05 | 0.0040643 | intron-variant | USP5 | GRCh38.p7 | 12:6860258 | GTCTAGGACCCTGTC[A/C]CTTTCAGGCCCTGGG | 8078 |
rs369088381 | snp | C/T | 9.89381e-05 | 0.00703273 | synonymous-codon, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6857685 | AGCCTGGCTGAGCAC[C/T]TGTCCCACTTCGGCA | 8078 |
rs369107454 | snp | C/T | 0.000182009 | 0.0095379 | synonymous-codon, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6864111 | CACAAGCGCAGCAGC[C/T]GACCCCCCTCCTGAG | 8078 |
rs369275986 | snp | G/T | 1.65427e-05 | 0.00287595 | intron-variant | USP5 | GRCh38.p7 | 12:6857748 | CCTTCAACTTCAGAT[G/T]CTTCTACTTCCTGCC | 8078 |
rs369321287 | snp | C/T | | | intron-variant | USP5 | GRCh38.p7 | 12:6857428 | ATTCCAACCCTCACC[C/T]GGTTTCATCTGTCTT | 8078 |
rs369337228 | snp | C/T | 8.47838e-05 | 0.00651036 | intron-variant | USP5 | GRCh38.p7 | 12:6864927 | ATCTGGTCAGTCTAC[C/T]ACACCAGATCCCTCA | 8078 |
rs369342704 | snp | C/T | | | intron-variant | USP5 | GRCh38.p7 | 12:6859597 | ATGGCCGTATACCTT[C/T]CTCCTCCCTGACCGC | 8078 |
rs369527996 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP5, CDCA3 | GRCh38.p7 | 12:6853285 | AGTCAGAGTGGAAAG[C/T]CTTCATTACTGCATC | 8078 |
rs369530493 | snp | C/T | 3.31868e-05 | 0.00407336 | synonymous-codon, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6860473 | GGAGTTCTTCCTTCA[C/T]CTTATCAACATGGTG | 8078 |
rs369587053 | snp | C/T | | | intron-variant | USP5 | GRCh38.p7 | 12:6862172 | TTGGTCTCTTAACTC[C/T]TGGGCTCAAGCAGTC | 8078 |
rs369704794 | snp | C/G | 0.000153988 | 0.00877328 | missense, upstream-variant-2KB, nc-transcript-variant | USP5, CDCA3 | GRCh38.p7 | 12:6852257 | TGGAGACCGGGTCCA[C/G]AAAGACGAGTGCGCC | 8078 |
rs369715672 | snp | C/T | 3.30246e-05 | 0.0040634 | intron-variant | USP5 | GRCh38.p7 | 12:6859422 | TCCTTCCCTTTTCCT[C/T]GGCGCTCAGGCCAGA | 8078 |
rs369739674 | snp | A/G | | | intron-variant | USP5 | GRCh38.p7 | 12:6858968 | CCCCACTGATAGTGC[A/G]GAGTGCCAAGTCCCA | 8078 |
rs369743798 | snp | A/C | 1.65239e-05 | 0.00287431 | intron-variant | USP5 | GRCh38.p7 | 12:6856181 | ATGCTACCCAAGATT[A/C]TAGAGCAAGATGGGC | 8078 |
rs369749430 | snp | A/G | 3.29592e-05 | 0.00405938 | missense, intron-variant, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6863326 | AGCCTTGGTTTCTAT[A/G]GCAACGAAGACGAAG | 8078 |
rs369790819 | snp | C/T | 1.64898e-05 | 0.00287135 | missense, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6856148 | GACATTGTCAGAGAT[C/T]GGGTATGACTGCCCC | 8078 |
rs369812300 | snp | C/T | 1.65589e-05 | 0.00287736 | intron-variant | USP5 | GRCh38.p7 | 12:6857755 | CTTCAGATTCTTCTA[C/T]TTCCTGCCCCTGTGA | 8078 |
rs369940936 | snp | C/G | | | intron-variant, upstream-variant-2KB | USP5, CDCA3 | GRCh38.p7 | 12:6853065 | ACCTCCCACACCATG[C/G]TTCACGTTTTGCAGG | 8078 |
rs370281885 | snp | C/G/T | 0.000169444 | 0.009203 | intron-variant | USP5 | GRCh38.p7 | 12:6865123 | ATCACTCAAGCATTC[C/G/T]TCTTCTGTTTCCTTC | 8078 |
rs370308880 | snp | G/T | | | intron-variant | USP5 | GRCh38.p7 | 12:6855178 | GTTCCTCAGCCCCCT[G/T]ATGTCCTTGTTGGTT | 8078 |
rs370315542 | snp | C/G | 1.65236e-05 | 0.00287429 | missense | USP5 | GRCh38.p7 | 12:6864839 | TCCATCTCTGAGTCT[C/G]TGCCAGTGGGACCTA | 8078 |
rs370387076 | snp | C/T | 1.6617e-05 | 0.00288239 | missense, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6855521 | CTCCGGCGGACCCGG[C/T]GCCCGGTAGGAGCAG | 8078 |
rs370406204 | snp | C/T | 0.00011565 | 0.00760339 | intron-variant | USP5 | GRCh38.p7 | 12:6861130 | CTCCATCAGCAAGGC[C/T]GTGGCACGGTGGGAG | 8078 |
rs370584513 | snp | A/G | | | intron-variant | USP5 | GRCh38.p7 | 12:6863131 | GGGATTGAGGTTCCC[A/G]AATCACTTTCCAGGT | 8078 |
rs370833306 | snp | C/G | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6856837 | GTGGAGCACTACCGA[C/G]AGACAGGCTACCCGT | 8078 |
rs370840242 | snp | C/T | 3.43708e-05 | 0.00414538 | synonymous-codon, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6863858 | TGAATCAGTCATCAT[C/T]CAGCTGGTGGAGATG | 8078 |
rs370907380 | snp | C/G | | | intron-variant | USP5 | GRCh38.p7 | 12:6860608 | GAACCCCAACAGTCT[C/G]TGTCCCTGTGAACAG | 8078 |
rs370956372 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | USP5 | GRCh38.p7 | 12:6856473 | CTGGCCCCTCTGCCT[C/T]GGGCACCACCCCCAG | 8078 |
rs371086459 | snp | C/T | 0.00115659 | 0.02402 | intron-variant, downstream-variant-500B | USP5 | GRCh38.p7 | 12:6864683 | GACAGAGCAAGACTC[C/T]GTCTCAAGAAAAAAA | 8078 |
rs371123912 | snp | C/G | 4.9423e-05 | 0.00497082 | upstream-variant-2KB, missense, utr-variant-5-prime, nc-transcript-variant | USP5, CDCA3 | GRCh38.p7 | 12:6850503 | GTGTCCGTGCAATAC[C/G]AAGAGTAGGAGAGCG | 8078 |
rs371130532 | snp | C/T | 3.29707e-05 | 0.00406008 | intron-variant | USP5 | GRCh38.p7 | 12:6859587 | GTTGACAGTCATGGC[C/T]GTATACCTTCCTCCT | 8078 |
rs371141015 | snp | A/C | 0.000153988 | 0.00877328 | intron-variant | USP5 | GRCh38.p7 | 12:6861399 | GCTAAGGAGGCAAAG[A/C]AGCAGCACCCTCCGA | 8078 |
rs371333696 | snp | C/G | 1.64781e-05 | 0.00287033 | intron-variant | USP5 | GRCh38.p7 | 12:6859456 | CCTCCAACTGTCCTT[C/G]CCTTGACTTTTAGGT | 8078 |
rs371404734 | snp | A/G | 3.29478e-05 | 0.00405867 | missense, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6856043 | GGATTTGACCTTAGC[A/G]AGGAGAAGTTTGAAT | 8078 |
rs371405607 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | USP5, CDCA3 | GRCh38.p7 | 12:6852022 | AAGCGCGGGGCAGGG[A/G]CGGAGCACCGGCAGG | 8078 |
rs371427595 | snp | C/T | 0.000437904 | 0.0147905 | intron-variant | USP5 | GRCh38.p7 | 12:6855698 | TTCCGTCCCTCCTCC[C/T]GACTTGTTCCTTCGC | 8078 |
rs371575316 | snp | A/G | 0.000153988 | 0.00877328 | synonymous-codon, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6855811 | GAAGAAGCCCACGCG[A/G]CTGGCTATTGGTGAG | 8078 |
rs371612920 | snp | C/T | 6.61387e-05 | 0.00575021 | intron-variant | USP5 | GRCh38.p7 | 12:6855867 | CTGAGCTGGTCTTTC[C/T]GGCTCTCAGCAGCAC | 8078 |
rs371648676 | snp | A/C/G | 3.36062e-05 | 0.00409905 | upstream-variant-2KB, missense, intron-variant, nc-transcript-variant | USP5, CDCA3 | GRCh38.p7 | 12:6850843 | AGTACCTGGATGGGA[A/C/G]TGCGCAGGATGCCAG | 8078 |
rs371661330 | snp | C/G | 0.000153988 | 0.00877328 | intron-variant | USP5 | GRCh38.p7 | 12:6860528 | CACCCCCATCTTCCT[C/G]CAATTTACTCGCTCT | 8078 |
rs371666955 | snp | C/G | 1.64814e-05 | 0.00287061 | missense, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6858493 | TGGGAGCTGATCCAG[C/G]AGTCAGGTGTGCCAC | 8078 |
rs371719487 | snp | A/C | | | upstream-variant-2KB, intron-variant | USP5, CDCA3 | GRCh38.p7 | 12:6851071 | ACCTTCAACCCTAAA[A/C]CACCCTGTCTTCCCA | 8078 |
rs371811102 | snp | C/T | | | upstream-variant-2KB, intron-variant | TPI1, USP5 | GRCh38.p7 | 12:6865676 | TCGTTGTGTCAGAGA[C/T]CAGAGAGAGAGCCTG | 8078 |
rs371981144 | snp | C/T | | | intron-variant | USP5 | GRCh38.p7 | 12:6858297 | TCAACATACCTCCCA[C/T]GTTTGAGCCTGTAAT | 8078 |
rs372092060 | snp | A/G | 6.82047e-05 | 0.00583932 | missense, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6861481 | AAGAAGCGGCAAGCC[A/G]AAGAGGAGAAGATGG | 8078 |
rs372106407 | snp | A/G | 0.000153988 | 0.00877328 | upstream-variant-2KB, intron-variant | USP5, CDCA3 | GRCh38.p7 | 12:6850796 | GAGACCCAAGAATTC[A/G]GACATTCTCTGCCTT | 8078 |
rs372248919 | snp | A/G | 3.55461e-05 | 0.00421566 | synonymous-codon, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6863831 | AATTCCCATTACAGC[A/G]CCCATGCTGGATGAA | 8078 |
rs372291004 | snp | C/T | 6.60524e-05 | 0.00574646 | intron-variant | USP5 | GRCh38.p7 | 12:6857609 | ACTTCCCCTGATTCT[C/T]TTCCTGCCTCCTGCT | 8078 |
rs372334756 | snp | C/T | 1.77628e-05 | 0.00298011 | intron-variant, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6863163 | GGCCTCCGGGAGCTG[C/T]TGAGGTGACCCTTTT | 8078 |
rs372470475 | snp | C/T | 0.000980296 | 0.0221176 | intron-variant, upstream-variant-2KB | USP5, CDCA3 | GRCh38.p7 | 12:6852313 | CATTCCCCACGCCCG[C/T]AACGAGCACGACTTC | 8078 |
rs372765750 | snp | A/G | 1.91174e-05 | 0.00309165 | intron-variant | USP5 | GRCh38.p7 | 12:6861659 | CTGTGGGTCTATGGC[A/G]GAGCTATCCCAGAGG | 8078 |
rs372777292 | snp | A/G | 8.24069e-05 | 0.00641846 | upstream-variant-2KB, synonymous-codon | TPI1, USP5 | GRCh38.p7 | 12:6866029 | TGCCTCCGAGAAGCC[A/G]CCCAAGGACCTGGGC | 8078 |
rs372791540 | snp | A/G | 3.46957e-05 | 0.00416493 | intron-variant | USP5 | GRCh38.p7 | 12:6864005 | AGCAGGGTGGGGCAG[A/G]GCCTCCATCCTCCCC | 8078 |
rs372825674 | snp | C/T | 3.30115e-05 | 0.00406259 | intron-variant | USP5 | GRCh38.p7 | 12:6856161 | ATCGGGTATGACTGC[C/T]CCCTATGCTACCCAA | 8078 |
rs372908566 | snp | C/T | 3.29723e-05 | 0.00406018 | synonymous-codon, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6857654 | ATATGATGAGGATGA[C/T]ATGGTCCTGGACCCC | 8078 |
rs373067555 | snp | C/T | 3.40159e-05 | 0.00412393 | intron-variant | USP5 | GRCh38.p7 | 12:6863399 | GACTCTTCTTCCTGC[C/T]TGTCTCTCTCCCGTG | 8078 |
rs373122898 | snp | A/G | 8.30806e-05 | 0.00644464 | synonymous-codon, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6856334 | GGAGGCCCTACTGTC[A/G]GCCGACTCAGCCTCC | 8078 |
rs373146270 | snp | A/C | 0.000416142 | 0.0144187 | upstream-variant-2KB, utr-variant-5-prime, intron-variant, nc-transcript-variant | USP5, CDCA3 | GRCh38.p7 | 12:6850989 | GGGGGCAAGGGCCAG[A/C]CCGGGACGAGGAGGG | 8078 |
rs373278331 | snp | A/G | | | intron-variant | USP5 | GRCh38.p7 | 12:6859722 | CAGTGGCGCGATCTC[A/G]GCTCACTACAACCTC | 8078 |
rs373298806 | in-del | -/A | | | intron-variant | USP5 | GRCh38.p7 | 12:6858858 | CCCTGTCTTCTCTTA[-/A]AAAAAAAAAAAGAAT | 8078 |
rs373307710 | snp | C/T | 8.24654e-05 | 0.00642074 | upstream-variant-2KB, intron-variant | USP5, CDCA3 | GRCh38.p7 | 12:6850429 | CCCAAGAATAATAGA[C/T]GACAGCTTCATCAGC | 8078 |
rs373377154 | snp | C/G | 6.73843e-05 | 0.0058041 | intron-variant | USP5 | GRCh38.p7 | 12:6858393 | CAGGGTTGAGTTTCT[C/G]ACTCAGTCTGAAGTG | 8078 |
rs373385702 | snp | A/G | 3.29995e-05 | 0.00406185 | missense, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6857703 | TCCCACTTCGGCATC[A/G]ACATGCTGAAGATGC | 8078 |
rs373402561 | snp | C/G | 0.000137193 | 0.00828116 | missense, upstream-variant-2KB, nc-transcript-variant | USP5, CDCA3 | GRCh38.p7 | 12:6852189 | GGTGTCATGGCGGAG[C/G]TGAGTGAGGAGGCGC | 8078 |
rs373444804 | snp | C/T | 1.64991e-05 | 0.00287215 | intron-variant | USP5 | GRCh38.p7 | 12:6859427 | CCCTTTTCCTCGGCG[C/T]TCAGGCCAGAGCCCC | 8078 |
rs373576214 | snp | A/G | 1.84018e-05 | 0.00303324 | intron-variant | USP5 | GRCh38.p7 | 12:6856938 | GCTTAAATATATTTC[A/G]TTTGTTAGTAATTTC | 8078 |
rs373638224 | snp | C/T | 3.29728e-05 | 0.00406021 | synonymous-codon, intron-variant, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6863331 | TGGTTTCTATGGCAA[C/T]GAAGACGAAGACTCC | 8078 |
rs373712824 | snp | A/G | 6.61059e-05 | 0.00574879 | intron-variant | USP5 | GRCh38.p7 | 12:6856191 | AGATTCTAGAGCAAG[A/G]TGGGCCAGGGTAGTG | 8078 |
rs373715705 | in-del | -/G | | | intron-variant | USP5 | GRCh38.p7 | 12:6859615 | CCTCCCTGACCGCCT[-/G]GGGGGCACAGCACTT | 8078 |
rs373775212 | snp | C/T | 3.44632e-05 | 0.00415095 | intron-variant | USP5 | GRCh38.p7 | 12:6864039 | ACACATCAACCCCTT[C/T]ACATCCACAGATTTT | 8078 |
rs373785473 | snp | C/T | 6.6496e-05 | 0.00576572 | missense, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6855525 | GGCGGACCCGGCGCC[C/T]GGTAGGAGCAGGGCT | 8078 |
rs373866739 | snp | C/G | 1.65507e-05 | 0.00287664 | missense, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6864129 | CCCCCCTCCTGAGGA[C/G]TGTGTGACCACCATT | 8078 |
rs373947454 | snp | C/G | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6856849 | CGAGAGACAGGCTAC[C/G]CGTTAGCTGTCAAGC | 8078 |
rs374114763 | snp | C/G | 3.34018e-05 | 0.00408654 | synonymous-codon, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6861519 | AGAACTGGTTCGGGC[C/G]CAGGTGCCCTTCAGC | 8078 |
rs374133197 | snp | A/C | 1.66905e-05 | 0.00288876 | intron-variant | USP5 | GRCh38.p7 | 12:6864892 | TGAGTATCCCCAGGA[A/C]GCAGGACAGGCCTGG | 8078 |
rs374138645 | snp | G/T | | | intron-variant | USP5 | GRCh38.p7 | 12:6857379 | CAAGCCTGTCTTACC[G/T]TATCCTATACAGGTA | 8078 |
rs374154051 | snp | A/G | 0.000198196 | 0.00995283 | intron-variant | USP5 | GRCh38.p7 | 12:6855831 | CTATTGGTGAGCACC[A/G]CTGCAGTCCTATTCT | 8078 |
rs374165611 | snp | C/T | 3.41437e-05 | 0.00413167 | missense, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6863958 | AACTGGGTCATGTCA[C/T]ACATGGATGATCCAG | 8078 |
rs374187489 | snp | A/G | 4.96479e-05 | 0.00498212 | missense | USP5 | GRCh38.p7 | 12:6864770 | TTCAGTCACATTGAC[A/G]ACCTGGATGCTGAAG | 8078 |
rs374324552 | snp | A/G | | | intron-variant | USP5 | GRCh38.p7 | 12:6860686 | TGGGCTTGAAGCCCA[A/G]TTCAGATTATGCCCA | 8078 |
rs374406508 | snp | A/C/T | 3.31638e-05 | 0.00407198 | intron-variant | USP5 | GRCh38.p7 | 12:6865150 | CTTCTCTGACCCCCT[A/C/T]TCTCCTTTCCTAGAG | 8078 |
rs374554839 | snp | C/T | | | intron-variant | USP5 | GRCh38.p7 | 12:6865305 | GGGAATGAGGAGGGC[C/T]ATTTGGAAGTCCTTG | 8078 |
rs374643076 | snp | C/T | 0.000153988 | 0.00877328 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | USP5, CDCA3 | GRCh38.p7 | 12:6852166 | CCGTGTGTGGAGAAG[C/T]TGCTGCCGGTGTCAT | 8078 |
rs374645378 | snp | C/T | 1.65165e-05 | 0.00287367 | intron-variant | USP5 | GRCh38.p7 | 12:6860242 | CCAGAACAGAAGGTG[C/T]GTCTAGGACCCTGTC | 8078 |
rs374666013 | snp | C/T | | | intron-variant | USP5 | GRCh38.p7 | 12:6863488 | CTCCCTTTCAAATTT[C/T]CTCTGCCCTCTTTGA | 8078 |
rs374755060 | snp | A/G | 5.38672e-05 | 0.00518948 | intron-variant | USP5 | GRCh38.p7 | 12:6863806 | CCAATCAGTCGGTCC[A/G]TGTACCCACAATTCC | 8078 |
rs375006887 | snp | C/T | 6.72721e-05 | 0.00579927 | intron-variant | USP5 | GRCh38.p7 | 12:6858395 | GGGTTGAGTTTCTCA[C/T]TCAGTCTGAAGTGCC | 8078 |
rs375025639 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | USP5 | GRCh38.p7 | 12:6861413 | GAAGCAGCACCCTCC[A/G]AAGGATCCACCAACC | 8078 |
rs375029370 | snp | A/G | 3.30814e-05 | 0.00406689 | intron-variant | USP5 | GRCh38.p7 | 12:6855966 | GCTCGGAGGAGGGAC[A/G]TTGACCTGTTGTCAT | 8078 |
rs375052469 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | USP5, CDCA3 | GRCh38.p7 | 12:6851766 | CTCGACTTTCCGACC[A/G]GACAGGTCCCCAGGA | 8078 |
rs375751858 | snp | G/T | 3.65999e-05 | 0.00427769 | intron-variant, upstream-variant-2KB | USP5, CDCA3 | GRCh38.p7 | 12:6852323 | GCCCGCAACGAGCAC[G/T]ACTTCCTTCCATCGC | 8078 |
rs375906700 | snp | A/G | 1.64727e-05 | 0.00286986 | synonymous-codon, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6856072 | ATTAGACGAGGATGT[A/G]AAGATTGTCATTTTG | 8078 |
rs376024668 | snp | A/G | 4.95683e-05 | 0.00497812 | intron-variant | USP5 | GRCh38.p7 | 12:6861131 | TCCATCAGCAAGGCC[A/G]TGGCACGGTGGGAGG | 8078 |
rs376054935 | snp | C/T | 1.69015e-05 | 0.00290696 | upstream-variant-2KB, intron-variant | USP5, CDCA3 | GRCh38.p7 | 12:6850817 | TCTCTGCCTTTCCCA[C/T]GCTGGCCCAGAGTAC | 8078 |
rs376068391 | snp | C/T | 1.67354e-05 | 0.00289265 | intron-variant | USP5 | GRCh38.p7 | 12:6855573 | CATTGTCTGTTCCAT[C/T]CTGACCTCCTATTGG | 8078 |
rs376152044 | snp | A/G | 1.65149e-05 | 0.00287353 | intron-variant | USP5 | GRCh38.p7 | 12:6857726 | GAAGATGCAGAAGGT[A/G]AGACCCCCTTCAACT | 8078 |
rs376215464 | snp | C/T | 0.000511007 | 0.0159763 | intron-variant | USP5 | GRCh38.p7 | 12:6859440 | CGCTCAGGCCAGAGC[C/T]CCTCCAACTGTCCTT | 8078 |
rs376240882 | snp | C/T | 1.6495e-05 | 0.0028718 | missense, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6858532 | CTGTTTGGGCCTGGC[C/T]ACACAGGCATCCGGA | 8078 |
rs376244475 | snp | A/G | 4.95503e-05 | 0.00497722 | missense | USP5 | GRCh38.p7 | 12:6864827 | TCAGCTGCCGACTCC[A/G]TCTCTGAGTCTGTGC | 8078 |
rs376272149 | snp | C/G | | | intron-variant | USP5 | GRCh38.p7 | 12:6859829 | AGCTAAATTTTTTTT[C/G]TATTTTTAGTAGAGA | 8078 |
rs376295117 | snp | C/G/T | 4.94754e-05 | 0.0049735 | missense, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6860207 | AGCCAGTACCGGAGT[C/G/T]GGGCGATGGGGAGCG | 8078 |
rs376349479 | snp | A/C | 4.94328e-05 | 0.00497131 | upstream-variant-2KB, missense, utr-variant-5-prime, nc-transcript-variant | USP5, CDCA3 | GRCh38.p7 | 12:6850595 | TGTGGAGAGCTCTCC[A/C]CCTGTCAAGACCATA | 8078 |
rs376412771 | snp | C/T | 0.00174248 | 0.0294653 | upstream-variant-2KB, intron-variant | USP5, CDCA3 | GRCh38.p7 | 12:6850415 | CTTCATGGACCCTAC[C/T]CAAGAATAATAGATG | 8078 |
rs376580038 | snp | A/G | 0.000115423 | 0.00759593 | upstream-variant-2KB, intron-variant | USP5, CDCA3 | GRCh38.p7 | 12:6850433 | AGAATAATAGATGAC[A/G]GCTTCATCAGCATTC | 8078 |
rs376721713 | snp | A/T | 0.000230635 | 0.0107361 | synonymous-codon, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6856761 | GTGGCTCAACCTGAC[A/T]GATGGCTCCATCCTC | 8078 |
rs376795145 | snp | A/T | 0.000153988 | 0.00877328 | intron-variant | USP5 | GRCh38.p7 | 12:6861626 | CTGTCAAGTAAGTCC[A/T]CTGGTCGGGGCCTGA | 8078 |
rs376973369 | snp | A/C | 1.69166e-05 | 0.00290827 | synonymous-codon, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6864066 | TTTTGCAAACCCCCT[A/C]ATCCTGCCTGGCTCT | 8078 |
rs377103167 | snp | C/T | 3.47222e-05 | 0.00416652 | intron-variant | USP5 | GRCh38.p7 | 12:6864014 | GGGCAGGGCCTCCAT[C/T]CTCCCCCAAACACAT | 8078 |
rs377118724 | snp | C/T | | | intron-variant, downstream-variant-500B | USP5 | GRCh38.p7 | 12:6864643 | GCAGTGAGCCGAGAT[C/T]GCGCCACTGCACTCC | 8078 |
rs377125153 | snp | G/T | | | intron-variant, upstream-variant-2KB | USP5, CDCA3 | GRCh38.p7 | 12:6853278 | AACTGCAAGTCAGAG[G/T]GGAAAGCCTTCATTA | 8078 |
rs377322447 | snp | C/T | 1.7351e-05 | 0.00294537 | synonymous-codon, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6863852 | GCTGGATGAATCAGT[C/T]ATCATCCAGCTGGTG | 8078 |
rs377361007 | snp | A/C/T | 3.32266e-05 | 0.00407583 | synonymous-codon, missense, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6855518 | CACCTCCGGCGGACC[A/C/T]GGCGCCCGGTAGGAG | 8078 |
rs377378758 | snp | A/T | 3.30049e-05 | 0.00406219 | intron-variant | USP5 | GRCh38.p7 | 12:6861119 | AAGGTAGGCTGCTCC[A/T]TCAGCAAGGCCGTGG | 8078 |
rs377393722 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | USP5 | GRCh38.p7 | 12:6855561 | AAGGCCTGGGTACAT[C/T]GTCTGTTCCATTCTG | 8078 |
rs377507262 | snp | G/T | 0.000437904 | 0.0147905 | upstream-variant-2KB, utr-variant-3-prime | TPI1, USP5 | GRCh38.p7 | 12:6866130 | GACCACCTGGCATGA[G/T]GGAGAGGGGCTGAGG | 8078 |
rs377552944 | snp | G/T | | | intron-variant | USP5 | GRCh38.p7 | 12:6854091 | AAAACTTGGTCAGCT[G/T]TGGGGGAAGCCCATC | 8078 |
rs377587665 | snp | C/T | 0.000153988 | 0.00877328 | synonymous-codon, intron-variant, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6863337 | CTATGGCAACGAAGA[C/T]GAAGACTCCTTCTGC | 8078 |
rs386375505 | in-del | -/GT | | | upstream-variant-2KB, intron-variant | USP5, CDCA3 | GRCh38.p7 | 12:6850171 | GCTTTTGTGTGTGTG[-/GT]TGTGTGTGTTATGTG | 8078 |
rs527313769 | snp | A/T | | | intron-variant, upstream-variant-2KB | USP5, TPI1 | GRCh38.p7 | 12:6865441 | CACCAGCTTTTTTTT[A/T]AAATAGAGATGGGAT | 8078 |
rs528906733 | snp | A/G | | | intron-variant | USP5 | GRCh38.p7 | 12:6854196 | CTCAGCAAGTGTTGC[A/G]AGATTGTTGTCAGAA | 8078 |
rs528919369 | snp | C/T | | | intron-variant | USP5 | GRCh38.p7 | 12:6856639 | GGGGGCCTGCAGAGC[C/T]CTCTCTCTCTGCCAC | 8078 |
rs529498494 | snp | C/T | 0.000215608 | 0.0103806 | intron-variant | USP5 | GRCh38.p7 | 12:6860911 | AGGCCCCATTCTGTT[C/T]CCTGGCTGCCCAGAC | 8078 |
rs529828085 | snp | A/C | | | intron-variant | USP5 | GRCh38.p7 | 12:6863528 | GGCCTCCCCAGCGCA[A/C]TCCTAGCCACCTTCT | 8078 |
rs530017359 | snp | A/G | 0.000132011 | 0.0081233 | intron-variant | USP5 | GRCh38.p7 | 12:6860108 | GGGACACACAGGGTC[A/G]TTAGTTGACTGAAGT | 8078 |
rs530703216 | snp | A/G | | | intron-variant | USP5 | GRCh38.p7 | 12:6857801 | GCCTGAGGCTGAGGT[A/G]GGGTTTTGGAGAAAT | 8078 |
rs531118465 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP5, CDCA3 | GRCh38.p7 | 12:6853186 | GCTTGGTTGGGATCC[A/G]CCCCCCTCACCACCC | 8078 |
rs532907416 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP5, CDCA3 | GRCh38.p7 | 12:6853927 | GCACTATTTTTCATA[C/T]CACAGCAGAGAAATG | 8078 |
rs533980054 | snp | G/T | | | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | USP5, CDCA3 | GRCh38.p7 | 12:6852011 | TGGCGTCAGTCAAGC[G/T]CGGGGCAGGGGCGGA | 8078 |
rs534115806 | snp | C/T | | | upstream-variant-2KB, intron-variant | TPI1, USP5 | GRCh38.p7 | 12:6865566 | CCGTGCCTGGCCAGG[C/T]CCCCTGCCTTTGTAA | 8078 |
rs534531204 | snp | A/G/T | | | intron-variant | USP5 | GRCh38.p7 | 12:6860846 | CTCTTGTGTCCCTGA[A/G/T]TTCCGAGTGGTAGTC | 8078 |
rs534798652 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | USP5, CDCA3 | GRCh38.p7 | 12:6851328 | GACCCTATTGGCTGA[A/G]CCGACGTAGTTCCCA | 8078 |
rs536110383 | snp | C/T | | | intron-variant | USP5 | GRCh38.p7 | 12:6858657 | AGGCCCCCTCCTGGT[C/T]AGCACCCTCTGGGCA | 8078 |
rs536635647 | snp | A/T | 1.65386e-05 | 0.00287559 | intron-variant | USP5 | GRCh38.p7 | 12:6855750 | CCCTTCCTGCTTCTT[A/T]ACAGAAAGAGGAGGA | 8078 |
rs537866918 | snp | C/T | | | intron-variant, downstream-variant-500B | USP5 | GRCh38.p7 | 12:6864667 | GCACTCCAGCCTGGG[C/T]GACAGAGCAAGACTC | 8078 |
rs537934479 | snp | A/G | 0.000362343 | 0.0134551 | synonymous-codon, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6861006 | CCGCTTCTTGGTGGA[A/G]GAAAAGATCAAGTGC | 8078 |
rs538768569 | snp | A/G | | | intron-variant | USP5 | GRCh38.p7 | 12:6858790 | TCGGGAGGCCAAGAT[A/G]GGAGAATTGCTTGAG | 8078 |
rs539840105 | snp | A/C | | | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | USP5, CDCA3 | GRCh38.p7 | 12:6851222 | ATTCAAATCACTTAC[A/C]GGGCCCCAATTCCAC | 8078 |
rs540092231 | snp | C/G/T | | | upstream-variant-2KB, intron-variant | TPI1, USP5 | GRCh38.p7 | 12:6865897 | AGAGTGTGGAGAGCA[C/G/T]TTCCAGGGGCCATGT | 8078 |
rs540692865 | snp | A/G | 6.65524e-05 | 0.00576817 | upstream-variant-2KB, intron-variant | TPI1, USP5 | GRCh38.p7 | 12:6865940 | ATGATGCCACTTTGA[A/G]TGCCCAGTTTGTTCA | 8078 |
rs541116715 | in-del | -/C | | | upstream-variant-2KB, utr-variant-3-prime | TPI1, USP5 | GRCh38.p7 | 12:6866464 | CGATCACCTGTGCCT[-/C]CCCTCCCCCTTTGTT | 8078 |
rs543937579 | snp | C/T | | | intron-variant | USP5 | GRCh38.p7 | 12:6863066 | CCCTAAGATGGGTGC[C/T]GTGCTTTTAGCAGCT | 8078 |
rs544486473 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP5, CDCA3 | GRCh38.p7 | 12:6853781 | TTACCTTCAAATTGG[A/G]CTCATGGTAGAAAGA | 8078 |
rs545579564 | snp | C/G | | | intron-variant, upstream-variant-2KB | USP5, CDCA3 | GRCh38.p7 | 12:6852992 | GTGGTTTCTTTCTCG[C/G]AGGATGCTAAGGCCT | 8078 |
rs546221115 | snp | C/T | | | intron-variant | USP5 | GRCh38.p7 | 12:6856899 | TGGAGCTGGTACAGC[C/T]TCCCCTCCTCCAGCC | 8078 |
rs546905871 | snp | C/T | | | intron-variant | USP5 | GRCh38.p7 | 12:6863668 | ATGGGCAGGGACCCA[C/T]ATTACAATTGTGTGG | 8078 |
rs547080960 | snp | A/G | | | intron-variant | USP5 | GRCh38.p7 | 12:6859935 | GCTGGGATTACAGGC[A/G]TGAGCCACCGTGCAC | 8078 |
rs548367738 | snp | A/G | | | intron-variant, downstream-variant-500B | USP5 | GRCh38.p7 | 12:6864638 | AGCTTGCAGTGAGCC[A/G]AGATCGCGCCACTGC | 8078 |
rs550810070 | in-del | -/T | | | intron-variant | USP5 | GRCh38.p7 | 12:6862083 | CCTCTCTGTGTGGGT[-/T]TTTTTTTTTTTTTCT | 8078 |
rs550929369 | snp | A/G | | | intron-variant | USP5 | GRCh38.p7 | 12:6858230 | GCCCTGATGACTAAC[A/G]GGCCTCTGGGACAAT | 8078 |
rs551469050 | snp | A/G | | | intron-variant | USP5 | GRCh38.p7 | 12:6857419 | TCACAAGTAATTCCA[A/G]CCCTCACCCGGTTTC | 8078 |
rs551607616 | snp | C/T | | | intron-variant | USP5 | GRCh38.p7 | 12:6854962 | TCTCCCATGAAGGGA[C/T]CCTTTTTCCCTTTGA | 8078 |
rs552541250 | snp | A/G | | | intron-variant | USP5 | GRCh38.p7 | 12:6854821 | ACACTCGGGTCAGAT[A/G]TACTGTTCAAGTGCT | 8078 |
rs553341287 | snp | C/T | | | intron-variant | USP5 | GRCh38.p7 | 12:6858736 | TAGAGTAGTTCCTAT[C/T]GGCTGGGTGTGTTGG | 8078 |
rs553786308 | snp | C/T | | | intron-variant | USP5 | GRCh38.p7 | 12:6861372 | ATACGGACACAGAGC[C/T]AGTAGGGAGAGGCTA | 8078 |
rs554148915 | snp | C/G | | | intron-variant | USP5 | GRCh38.p7 | 12:6861271 | CTCGTCCAGTGGACA[C/G]TCAGCTTGTTAGCAG | 8078 |
rs554351283 | snp | A/G | | | upstream-variant-2KB, intron-variant | TPI1, USP5 | GRCh38.p7 | 12:6866714 | AAAACTCCTAACTCT[A/G]GCCGCCTCCCTGCCA | 8078 |
rs554491195 | snp | C/T | | | upstream-variant-2KB, intron-variant | TPI1, USP5 | GRCh38.p7 | 12:6865645 | CCTGTTTTCACGCTG[C/T]GGCAGGAAAGTTGAG | 8078 |
rs554897845 | snp | C/T | | | synonymous-codon, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6859494 | TAAGCTGGAGAAGAT[C/T]TTCCAGAATGCCCCG | 8078 |
rs555006477 | snp | C/T | | | intron-variant | USP5 | GRCh38.p7 | 12:6859333 | GTTGCTGGAGAGAAG[C/T]GACTCCAAGGTTCAC | 8078 |
rs556207552 | snp | C/T | | | intron-variant, downstream-variant-500B | USP5 | GRCh38.p7 | 12:6864464 | GGAGGGTGAGGTGGG[C/T]GGATCACGCGGTCAG | 8078 |
rs558127475 | snp | A/C | | | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | USP5, CDCA3 | GRCh38.p7 | 12:6851679 | GTTGACAGCTGTATC[A/C]GTCACTCGACACAAC | 8078 |
rs558200005 | in-del | -/C | | | upstream-variant-2KB, intron-variant | USP5, CDCA3 | GRCh38.p7 | 12:6850305 | TACAGGCATGAGCCA[-/C]CCGCACCCAGGCTGG | 8078 |
rs558401327 | in-del | -/C | | | intron-variant, downstream-variant-500B | USP5 | GRCh38.p7 | 12:6864493 | GCAGATCAAGACCAT[-/C]CCTGGCTAACACGGT | 8078 |
rs558740385 | snp | G/T | | | synonymous-codon, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6856379 | GCAGGCATGGGATGG[G/T]GAAGTACGGCAGGTG | 8078 |
rs559042986 | snp | A/G | | | intron-variant | USP5 | GRCh38.p7 | 12:6857305 | TCAAAAAAGGAAAAT[A/G]CTGCAGATGAGACTA | 8078 |
rs559317731 | snp | C/G | | | intron-variant | USP5 | GRCh38.p7 | 12:6859642 | ACTTTAACCCCTGGC[C/G]TTTTTTTGTTTTGTT | 8078 |
rs561157955 | snp | A/G | | | intron-variant | USP5 | GRCh38.p7 | 12:6863092 | CAGCTCCTCTTTACA[A/G]AGCAGTTCTGACATA | 8078 |
rs562379237 | snp | C/T | | | intron-variant | USP5 | GRCh38.p7 | 12:6862996 | TGGTAGATCTAGGAC[C/T]AGCATCCTGGCCTCC | 8078 |
rs562492316 | snp | A/G | | | missense, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6863215 | ATGCCAGAGGAGCTC[A/G]ACATCTCCCAGTTGA | 8078 |
rs565020745 | snp | A/G | | | intron-variant | USP5 | GRCh38.p7 | 12:6862309 | TGCTCCTCGTTGGCC[A/G]AGGACAGGCATCAGA | 8078 |
rs565223479 | snp | A/C/G | 3.29501e-05 | 0.00405884 | upstream-variant-2KB, missense, utr-variant-5-prime, nc-transcript-variant | USP5, CDCA3 | GRCh38.p7 | 12:6850518 | CAAGAGTAGGAGAGC[A/C/G]GGGATCTGAGTCCTG | 8078 |
rs565755536 | snp | C/G | | | intron-variant | USP5 | GRCh38.p7 | 12:6854207 | TTGCGAGATTGTTGT[C/G]AGAACGGGATGGCTT | 8078 |
rs565763194 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | USP5, CDCA3 | GRCh38.p7 | 12:6851278 | TCAACTCCCGAAGTT[A/G]CCAGTTTCAAACTTC | 8078 |
rs568667985 | snp | A/G | 1.67998e-05 | 0.00289821 | missense | USP5 | GRCh38.p7 | 12:6864725 | TTCCTCTCCAAGAAC[A/G]ATAGTTTAGAACGGG | 8078 |
rs569183463 | snp | C/T | | | intron-variant, downstream-variant-500B | USP5 | GRCh38.p7 | 12:6864650 | GCCGAGATCGCGCCA[C/T]TGCACTCCAGCCTGG | 8078 |
rs571489686 | snp | A/C | | | intron-variant | USP5 | GRCh38.p7 | 12:6857518 | ACCAAGAGGGTGGAC[A/C]TTACTGGCTCTCCTT | 8078 |
rs573945934 | snp | C/G | | | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | USP5, CDCA3 | GRCh38.p7 | 12:6851868 | TCTAAGGGTCCCGGA[C/G]CCGGAGCAGCTGCGG | 8078 |
rs574311901 | snp | C/T | | | intron-variant, downstream-variant-500B | USP5 | GRCh38.p7 | 12:6864637 | GAGCTTGCAGTGAGC[C/T]GAGATCGCGCCACTG | 8078 |
rs574813090 | snp | C/T | 0.000150445 | 0.00867179 | intron-variant | USP5 | GRCh38.p7 | 12:6855570 | GTACATTGTCTGTTC[C/T]ATTCTGACCTCCTAT | 8078 |
rs574902679 | snp | C/T | | | intron-variant | USP5 | GRCh38.p7 | 12:6860579 | TCTATCAGCCCCAAC[C/T]CAGTCCCATCCCTGA | 8078 |
rs575283838 | snp | C/T | | | upstream-variant-2KB, utr-variant-3-prime | TPI1, USP5 | GRCh38.p7 | 12:6866413 | GGTCTCGTTTGTGCG[C/T]GTGGGTGTAGCTTTG | 8078 |
rs575404753 | snp | G/T | 1.67044e-05 | 0.00288997 | missense, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6856418 | TGCCTTCAGCCTCAA[G/T]CAGTTGGACAACCCT | 8078 |
rs745902418 | snp | A/G | | | intron-variant | USP5 | GRCh38.p7 | 12:6858057 | GGCGGAGGGTACTAC[A/G]GTAATTGACAGCAGG | 8078 |
rs746003386 | snp | C/T | | | intron-variant | USP5 | GRCh38.p7 | 12:6863130 | GGGGATTGAGGTTCC[C/T]GAATCACTTTCCAGG | 8078 |
rs747071390 | in-del | -/G | | | intron-variant, upstream-variant-2KB | USP5, CDCA3 | GRCh38.p7 | 12:6853371 | ATTTGTGGTTTGCTT[-/G]GTTTGCTAGGCTTTG | 8078 |
rs747921762 | in-del | -/TGCCTTCGT | | | intron-variant, upstream-variant-2KB | USP5, CDCA3 | GRCh38.p7 | 12:6852541 | ATTGTAGTCACTCAC[-/TGCCTTCGT]TGCCGTTCTAAGCTA | 8078 |
rs749961570 | snp | A/T | | | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | USP5, CDCA3 | GRCh38.p7 | 12:6851299 | TTCAAACTTCCCGCC[A/T]CGCCCCCTGCCCTGA | 8078 |
rs751290389 | snp | A/G | | | intron-variant | USP5 | GRCh38.p7 | 12:6862131 | TGTTTTTTTCCCTAC[A/G]TGTGGGTCTTGCTAT | 8078 |
rs751437211 | snp | G/T | | | upstream-variant-2KB, intron-variant | TPI1, USP5 | GRCh38.p7 | 12:6866745 | AAGTCAAGTCTCCAC[G/T]TTTCACTGGTTCTAG | 8078 |
rs752040428 | snp | C/T | | | intron-variant | USP5 | GRCh38.p7 | 12:6855954 | AGTGAGGTGCTGGCT[C/T]GGAGGAGGGACATTG | 8078 |
rs752329524 | snp | C/T | | | intron-variant | USP5 | GRCh38.p7 | 12:6860632 | TGAACAGTGCTTGCA[C/T]CTGAGGAGGACAGTG | 8078 |
rs752595305 | snp | C/T | | | missense, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6856350 | GCCGACTCAGCCTCC[C/T]GCAAGCAGGAGGTGC | 8078 |
rs753222013 | snp | C/T | | | upstream-variant-2KB, intron-variant | USP5, CDCA3 | GRCh38.p7 | 12:6850659 | CCTCTCCTCCCCATA[C/T]TCCAGGAAGGAATTG | 8078 |
rs754718964 | snp | C/T | 0.000181358 | 0.00952083 | synonymous-codon, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6856147 | TGACATTGTCAGAGA[C/T]CGGGTATGACTGCCC | 8078 |
rs754751251 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | USP5, CDCA3 | GRCh38.p7 | 12:6851948 | TCCCGCCCTGGAGGA[A/G]TGGGATTGGTTCTTT | 8078 |
rs755595731 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | USP5, CDCA3 | GRCh38.p7 | 12:6851603 | AGTGATTACACTATT[A/G]TGCGCACATCCAGCT | 8078 |
rs757258109 | snp | A/G | | | intron-variant | USP5 | GRCh38.p7 | 12:6862188 | TGGGCTCAAGCAGTC[A/G]TCCTGCCTTGGCCTC | 8078 |
rs758298170 | snp | G/T | | | intron-variant | USP5 | GRCh38.p7 | 12:6860807 | TGGGGAGGGGTTGGT[G/T]AATTAGGGAAGGTTT | 8078 |
rs759118336 | snp | C/G | | | missense | USP5 | GRCh38.p7 | 12:6864815 | TCAGAGGGCCGCTCA[C/G]CTGCCGACTCCATCT | 8078 |
rs759750824 | snp | C/G | | | intron-variant | USP5 | GRCh38.p7 | 12:6854917 | GGTGTCCCCTGGTTT[C/G]GGTTCAGTGTCTCAC | 8078 |
rs759824604 | snp | C/G | | | upstream-variant-2KB, intron-variant | USP5, CDCA3 | GRCh38.p7 | 12:6850270 | CGATCTGACCACCCC[C/G]GCCTTCCAACGTGCT | 8078 |
rs760138071 | snp | A/G | | | intron-variant | USP5 | GRCh38.p7 | 12:6855955 | GTGAGGTGCTGGCTC[A/G]GAGGAGGGACATTGA | 8078 |
rs762432005 | snp | C/T | | | intron-variant | USP5 | GRCh38.p7 | 12:6859858 | GACGGGGTTTCATCA[C/T]GTTGGCCAGGATGGT | 8078 |
rs763297879 | snp | G/T | | | intron-variant | USP5 | GRCh38.p7 | 12:6855180 | TCCTCAGCCCCCTGA[G/T]GTCCTTGTTGGTTGT | 8078 |
rs764601063 | snp | C/G/T | 4.95146e-05 | 0.00497547 | synonymous-codon, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6855484 | ACATTTCAATAAGAC[C/G/T]GGCCAGCGAGTCTAC | 8078 |
rs764796082 | snp | C/T | | | intron-variant | USP5 | GRCh38.p7 | 12:6864993 | TTCTTTCCACCTCAA[C/T]GTGGCATCTGAGGGT | 8078 |
rs768844435 | snp | A/G | | | intron-variant | USP5 | GRCh38.p7 | 12:6863702 | TTTTGGTTTTGGGAT[A/G]AGGTGCCAATCCATG | 8078 |
rs769799793 | snp | G/T | | | intron-variant | USP5 | GRCh38.p7 | 12:6863397 | GTGACTCTTCTTCCT[G/T]CCTGTCTCTCTCCCG | 8078 |
rs770934365 | snp | C/G | | | intron-variant | USP5 | GRCh38.p7 | 12:6857054 | ACTTTGGGAGGCCAA[C/G]GCAGGAGAATTGCTT | 8078 |
rs775299694 | snp | C/G | | | intron-variant | USP5 | GRCh38.p7 | 12:6865406 | TTGCAGCAGTGATTG[C/G]CCCAAGGGTTGGATC | 8078 |
rs778901458 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | USP5, CDCA3 | GRCh38.p7 | 12:6851987 | AATTGCCTTAGGAGC[A/G]CTTCTCATTGGCGTC | 8078 |
rs780286963 | snp | A/G | | | intron-variant | USP5 | GRCh38.p7 | 12:6863452 | GCATCCCCTGCCCCT[A/G]TCCTTTGTGTTTCTC | 8078 |
rs781377454 | snp | A/C | | | intron-variant | USP5 | GRCh38.p7 | 12:6857435 | CCCTCACCCGGTTTC[A/C]TCTGTCTTCCCTGAC | 8078 |
rs781784628 | snp | C/T | 1.67587e-05 | 0.00289466 | missense, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6863910 | CGCAAAGCTGTCTAC[C/T]ACACGGGCAACAGCG | 8078 |
rs781785222 | snp | C/T | 1.80798e-05 | 0.00300658 | intron-variant | USP5 | GRCh38.p7 | 12:6861424 | CTCCGAAGGATCCAC[C/T]AACCCATTCTGTCAC | 8078 |
rs781788655 | snp | C/T | 1.65562e-05 | 0.00287712 | missense, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6855503 | CAGCGAGTCTACTTG[C/T]ACCTCCGGCGGACCC | 8078 |
rs781789071 | snp | A/G | 1.65102e-05 | 0.00287312 | intron-variant | USP5 | GRCh38.p7 | 12:6860243 | CAGAACAGAAGGTGC[A/G]TCTAGGACCCTGTCC | 8078 |
rs781789969 | snp | A/G | | | intron-variant | USP5 | GRCh38.p7 | 12:6859191 | GCTCAGAACATGTCA[A/G]CAGGTTCTGTCCAAT | 8078 |
rs781789972 | snp | A/G | 3.42906e-05 | 0.00414055 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | USP5, CDCA3 | GRCh38.p7 | 12:6852134 | GCAGGGGAGGGGACT[A/G]GGAACGGTGGGAGCC | 8078 |
rs781790061 | snp | A/C/T | 4.95498e-05 | 0.00497723 | intron-variant | USP5 | GRCh38.p7 | 12:6862588 | ATGAGGGAGGTTACA[A/C/T]AGAAAATGCTAGAAA | 8078 |
rs781790912 | snp | A/G | | | upstream-variant-2KB, intron-variant | TPI1, USP5 | GRCh38.p7 | 12:6865793 | GTACTGGAGGATCTG[A/G]AGACATAATAGGGTC | 8078 |
rs781791457 | snp | C/G | 1.64765e-05 | 0.00287019 | upstream-variant-2KB, missense, utr-variant-5-prime, nc-transcript-variant | USP5, CDCA3 | GRCh38.p7 | 12:6850557 | TAAGACCCTCCAGTT[C/G]CTCCCCTGCTGGTAG | 8078 |
rs781792354 | snp | A/G | | | intron-variant | USP5 | GRCh38.p7 | 12:6855212 | ATCAAAGTCATGGGA[A/G]GAAATGGGGAGAATC | 8078 |
rs781792728 | snp | A/C | 1.95521e-05 | 0.0031266 | intron-variant | USP5 | GRCh38.p7 | 12:6858639 | AGTGCCCTCTCCTTC[A/C]CCAGGCCCCCTCCTG | 8078 |
rs781793501 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP5, CDCA3 | GRCh38.p7 | 12:6852495 | GCCGCGCTCACCTCT[C/T]CGGCTCCCCGCTTCG | 8078 |
rs781793539 | in-del | -/C | 1.65218e-05 | 0.00287413 | intron-variant | USP5 | GRCh38.p7 | 12:6857729 | ATGCAGAAGGTGAGA[-/C]CCCCCTTCAACTTCA | 8078 |
rs781796767 | snp | A/G | | | missense, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6855810 | GGAAGAAGCCCACGC[A/G]GCTGGCTATTGGTGA | 8078 |
rs781797393 | snp | A/G | 1.6857e-05 | 0.00290314 | intron-variant | USP5 | GRCh38.p7 | 12:6864917 | GCCTGGTGGAATCTG[A/G]TCAGTCTACTACACC | 8078 |
rs781797847 | snp | A/G | 1.64866e-05 | 0.00287106 | intron-variant | USP5 | GRCh38.p7 | 12:6860144 | GTTTTCTTGGATATT[A/G]ATGCAGGGCCAAGCT | 8078 |
rs781799228 | snp | G/T | 1.67058e-05 | 0.00289009 | intron-variant | USP5 | GRCh38.p7 | 12:6860532 | CCCATCTTCCTGCAA[G/T]TTACTCGCTCTCCTT | 8078 |
rs781800281 | snp | A/G | 5.1133e-05 | 0.00505608 | missense, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6864188 | CCTTGAAAGCGCTGC[A/G]GGCCACGGTATGGGC | 8078 |
rs781800404 | snp | C/T | | | intron-variant | USP5 | GRCh38.p7 | 12:6859623 | ACCGCCTGGGGGGCA[C/T]AGCACTTTAACCCCT | 8078 |
rs781801249 | snp | G/T | | | intron-variant | USP5 | GRCh38.p7 | 12:6859920 | TCGGCCTCCCAAAGT[G/T]CTGGGATTACAGGCG | 8078 |
rs781802636 | snp | A/C | | | intron-variant, downstream-variant-500B | USP5 | GRCh38.p7 | 12:6864457 | CACTTTGGGAGGGTG[A/C]GGTGGGCGGATCACG | 8078 |
rs781804761 | snp | C/T | | | intron-variant | USP5 | GRCh38.p7 | 12:6862884 | AGAACTCGTGATGTA[C/T]CTTCATTTTCTAGAT | 8078 |
rs781808082 | snp | A/G | 6.62537e-05 | 0.00575521 | missense, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6864101 | GGCCGGGCTCCACAA[A/G]CGCAGCAGCCGACCC | 8078 |
rs781808533 | snp | A/G | 1.64844e-05 | 0.00287087 | upstream-variant-2KB, intron-variant | USP5, CDCA3 | GRCh38.p7 | 12:6850626 | GGCTAGAACAAGTCT[A/G]GGCCCTGACTCTTCT | 8078 |
rs781808600 | snp | G/T | | | intron-variant | USP5 | GRCh38.p7 | 12:6859091 | GCACTTGGGGAGGAG[G/T]GGGGCTTGGCACACT | 8078 |
rs781809049 | snp | C/T | 3.64053e-05 | 0.0042663 | intron-variant, upstream-variant-2KB | USP5, CDCA3 | GRCh38.p7 | 12:6852322 | CGCCCGCAACGAGCA[C/T]GACTTCCTTCCATCG | 8078 |
rs781809116 | snp | A/G | | | intron-variant | USP5 | GRCh38.p7 | 12:6861219 | TGCTTCACCAGCCAA[A/G]GTTCCAGTCTGGGCC | 8078 |
rs781810764 | snp | C/T | 1.68114e-05 | 0.00289921 | synonymous-codon, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6861552 | TTGCCTGGAGGCCTA[C/T]GGGGCCCCTGAGCAG | 8078 |
rs781812005 | snp | A/T | 1.64738e-05 | 0.00286995 | missense, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6856044 | GATTTGACCTTAGCG[A/T]GGAGAAGTTTGAATT | 8078 |
rs781812076 | snp | C/T | | | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | USP5, CDCA3 | GRCh38.p7 | 12:6851475 | CCTCCTTGATAAGGG[C/T]ACTTCTGTTCAGTAT | 8078 |
rs781815396 | snp | A/G | 1.75084e-05 | 0.0029587 | upstream-variant-2KB, missense, intron-variant, nc-transcript-variant | USP5, CDCA3 | GRCh38.p7 | 12:6850909 | TGCTTGTTGTGCGGC[A/G]GAGGCCGCGCTGGTG | 8078 |
rs781816036 | snp | G/T | 1.66288e-05 | 0.00288343 | missense, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6856330 | CAGTGGAGGCCCTAC[G/T]GTCGGCCGACTCAGC | 8078 |
rs781818028 | snp | C/T | 8.97368e-05 | 0.00669779 | intron-variant | USP5 | GRCh38.p7 | 12:6863807 | CAATCAGTCGGTCCG[C/T]GTACCCACAATTCCC | 8078 |
rs781819637 | snp | A/G | 1.65018e-05 | 0.00287239 | intron-variant | USP5 | GRCh38.p7 | 12:6855397 | CTTACCTCTTGTCCC[A/G]CAGGAGTCTGAGGGG | 8078 |
rs781820814 | snp | C/T | | | intron-variant | USP5 | GRCh38.p7 | 12:6855658 | TTTTTAGCTTTATTC[C/T]GTTCTGAGATGAAGC | 8078 |
rs781821230 | snp | C/T | 1.77843e-05 | 0.00298191 | intron-variant, downstream-variant-500B | USP5 | GRCh38.p7 | 12:6864681 | GCGACAGAGCAAGAC[C/T]CCGTCTCAAGAAAAA | 8078 |
rs781821563 | snp | C/G | | | intron-variant | USP5 | GRCh38.p7 | 12:6862017 | AAAGGGCTTTGGTCT[C/G]GGGGAGTCAGCTACC | 8078 |
rs781823151 | snp | A/G | 4.95152e-05 | 0.00497545 | synonymous-codon | USP5 | GRCh38.p7 | 12:6865171 | TTTCCTAGAGTATCA[A/G]CTCTTTGCCTTCATT | 8078 |
rs781823697 | snp | C/T | 3.31027e-05 | 0.0040682 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | USP5, CDCA3 | GRCh38.p7 | 12:6852132 | GGGCAGGGGAGGGGA[C/T]TGGGAACGGTGGGAG | 8078 |
rs781825607 | snp | A/C/G | 3.29518e-05 | 0.00405894 | intron-variant | USP5 | GRCh38.p7 | 12:6862450 | ATTGTCTGGGTACCA[A/C/G]CACAGTCTCTCTTCC | 8078 |
rs781827269 | snp | C/T | | | intron-variant | USP5 | GRCh38.p7 | 12:6857788 | GCCCTTCCTCTTTGC[C/T]TGAGGCTGAGGTAGG | 8078 |
rs781827570 | snp | C/T | 1.64765e-05 | 0.00287019 | missense, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6863302 | GTCACTCCGGATGAG[C/T]CCAAAGGTAGCCTTG | 8078 |
rs781828767 | snp | C/T | 8.23744e-05 | 0.0064172 | synonymous-codon, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6856764 | GCTCAACCTGACTGA[C/T]GGCTCCATCCTCTGT | 8078 |
rs781828887 | snp | A/G/T | 0.000131792 | 0.00811666 | intron-variant | USP5 | GRCh38.p7 | 12:6859559 | ATGTAACCAGGTCCT[A/G/T]TGTAGGAAAGCTGTT | 8078 |
rs781829502 | snp | A/G | 1.65523e-05 | 0.00287678 | intron-variant | USP5 | GRCh38.p7 | 12:6860923 | GTTCCCTGGCTGCCC[A/G]GACCTCCCTACCCTG | 8078 |
rs781830321 | snp | A/G | | | upstream-variant-2KB, intron-variant | TPI1, USP5 | GRCh38.p7 | 12:6865646 | CTGTTTTCACGCTGC[A/G]GCAGGAAAGTTGAGT | 8078 |
rs781831858 | snp | A/G | | | intron-variant | USP5 | GRCh38.p7 | 12:6856961 | GTAATTTCGTGTGAC[A/G]TGTATAATACATGAA | 8078 |
rs781832956 | snp | C/T | 1.64768e-05 | 0.00287021 | synonymous-codon, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6856752 | AGAGAACCTGTGGCT[C/T]AACCTGACTGATGGC | 8078 |
rs781834108 | snp | A/C | | | synonymous-codon, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6864147 | TGTGACCACCATTGT[A/C]TCCATGGGCTTCTCC | 8078 |
rs781837325 | snp | A/G | 1.64727e-05 | 0.00286986 | synonymous-codon, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6856087 | GAAGATTGTCATTTT[A/G]CCAGATTACCTGGAG | 8078 |
rs781837614 | snp | A/C | | | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | USP5, CDCA3 | GRCh38.p7 | 12:6851939 | TACGTGCGCTCCCGC[A/C]CTGGAGGAGTGGGAT | 8078 |
rs781837647 | snp | C/T | 1.67536e-05 | 0.00289423 | intron-variant | USP5 | GRCh38.p7 | 12:6858401 | AGTTTCTCACTCAGT[C/T]TGAAGTGCCCCTTCT | 8078 |
rs781837779 | snp | C/G | | | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | USP5, CDCA3 | GRCh38.p7 | 12:6852032 | CAGGGGCGGAGCACC[C/G]GCAGGCAGGCTCCGT | 8078 |
rs781839069 | snp | A/C | 1.64738e-05 | 0.00286995 | intron-variant | USP5 | GRCh38.p7 | 12:6859552 | CAGGTGTATGTAACC[A/C]GGTCCTATGTAGGAA | 8078 |
rs781840035 | snp | A/G | 3.33056e-05 | 0.00408065 | intron-variant | USP5 | GRCh38.p7 | 12:6855538 | CCCGGTAGGAGCAGG[A/G]CTGGGGCAAGGCCTG | 8078 |
rs781843297 | snp | A/G | 1.64822e-05 | 0.00287068 | upstream-variant-2KB, synonymous-codon | TPI1, USP5 | GRCh38.p7 | 12:6866008 | CTACAATGACCAGAA[A/G]GTGTGTGCCTCCGAG | 8078 |
rs781843611 | snp | C/T | 1.74455e-05 | 0.00295338 | intron-variant | USP5 | GRCh38.p7 | 12:6856467 | TGAGGCCTGGCCCCT[C/T]TGCCTCGGGCACCAC | 8078 |
rs781846235 | snp | C/T | | | intron-variant | USP5 | GRCh38.p7 | 12:6863042 | GTATTATTTGTCTTA[C/T]ACTGGGACCCCTAAG | 8078 |
rs781847833 | snp | A/G | 1.97276e-05 | 0.0031406 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | USP5, CDCA3 | GRCh38.p7 | 12:6852230 | ATTACCGACGATCCG[A/G]GTCCCTAAGGCTGGA | 8078 |
rs781848501 | snp | C/G | 1.65263e-05 | 0.00287452 | intron-variant | USP5 | GRCh38.p7 | 12:6856186 | ACCCAAGATTCTAGA[C/G]CAAGATGGGCCAGGG | 8078 |
rs781850878 | snp | A/C | 6.5937e-05 | 0.00574144 | missense, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6856723 | GGCTGGAAGTGCTCC[A/C]AGTGTGACATGAGAG | 8078 |
rs781851417 | snp | C/T | 6.86047e-05 | 0.00585642 | missense, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6864194 | AAGCGCTGCGGGCCA[C/T]GGTATGGGCTGCCCC | 8078 |
rs781853920 | snp | G/T | 1.68926e-05 | 0.0029062 | intron-variant | USP5 | GRCh38.p7 | 12:6864922 | GTGGAATCTGGTCAG[G/T]CTACTACACCAGATC | 8078 |
rs781854365 | snp | G/T | | | intron-variant | USP5 | GRCh38.p7 | 12:6859674 | TGTTTTGTTTTTTGA[G/T]ACGGAGTCTTGTTCT | 8078 |
rs781856774 | snp | A/G | 1.64727e-05 | 0.00286986 | missense, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6856064 | AAGTTTGAATTAGAC[A/G]AGGATGTGAAGATTG | 8078 |
rs781857059 | snp | C/T | 3.30825e-05 | 0.00406696 | upstream-variant-2KB, intron-variant | TPI1, USP5 | GRCh38.p7 | 12:6865962 | GTTTGTTCATCCTTT[C/T]CTGTTTTCCCCACTT | 8078 |
rs781857067 | snp | C/G | 1.71905e-05 | 0.00293172 | missense, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6856450 | CTCGAATCCCTCCCT[C/G]GTGAGGCCTGGCCCC | 8078 |
rs781857109 | snp | C/T | | | intron-variant | USP5 | GRCh38.p7 | 12:6862784 | ATTTTTGTAGTTTTT[C/T]AAAATAATTGGTAAA | 8078 |
rs781858031 | snp | A/G | | | intron-variant | USP5 | GRCh38.p7 | 12:6858983 | AGAGTGCCAAGTCCC[A/G]GGGCTCTGTGGCCTT | 8078 |
rs781858281 | snp | A/G | | | upstream-variant-2KB, utr-variant-3-prime | TPI1, USP5 | GRCh38.p7 | 12:6866354 | AATCCACAGTGCTCT[A/G]CTTCTCTGTGTCGCC | 8078 |
rs781860852 | snp | C/T | 1.65233e-05 | 0.00287426 | synonymous-codon | USP5 | GRCh38.p7 | 12:6864790 | GGATGCTGAAGCTGC[C/T]ATGGACATCTCAGAG | 8078 |
rs781862376 | snp | A/G | 1.8181e-05 | 0.00301499 | intron-variant, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6863145 | CGAATCACTTTCCAG[A/G]TAGGCCTCCGGGAGC | 8078 |
rs781865814 | snp | C/T | 1.65048e-05 | 0.00287265 | missense, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6860390 | GATGGCATTGCCCCT[C/T]GGATGTTCAAGGCCC | 8078 |
rs781866897 | snp | C/G | 3.52448e-05 | 0.00419775 | upstream-variant-2KB, missense, intron-variant, nc-transcript-variant | USP5, CDCA3 | GRCh38.p7 | 12:6850916 | TGTGCGGCGGAGGCC[C/G]CGCTGGTGTGACTGG | 8078 |
rs781867359 | snp | A/G | | | intron-variant | USP5 | GRCh38.p7 | 12:6863067 | CCTAAGATGGGTGCC[A/G]TGCTTTTAGCAGCTC | 8078 |
rs781867922 | snp | C/G | 1.64779e-05 | 0.00287031 | intron-variant | USP5 | GRCh38.p7 | 12:6859457 | CTCCAACTGTCCTTC[C/G]CTTGACTTTTAGGTA | 8078 |
rs781868133 | snp | A/T | | | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | USP5, CDCA3 | GRCh38.p7 | 12:6851361 | GGCCCTCCACGTAAG[A/T]CCCGCCTCGAGCCAA | 8078 |
rs781869511 | snp | A/G | 1.65957e-05 | 0.00288055 | synonymous-codon, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6855511 | CTACTTGCACCTCCG[A/G]CGGACCCGGCGCCCG | 8078 |
rs781869631 | snp | C/G | | | intron-variant | USP5 | GRCh38.p7 | 12:6862223 | AGTGCTGGAATTACA[C/G]ATATGAGCCACCATG | 8078 |
rs781869988 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP5, CDCA3 | GRCh38.p7 | 12:6853550 | CTCCCACATTCTTCC[C/T]AGGAGGGAAAGGTTT | 8078 |
rs781871819 | snp | A/G | | | upstream-variant-2KB, missense, utr-variant-5-prime, nc-transcript-variant | USP5, CDCA3 | GRCh38.p7 | 12:6850578 | CTGCTGGTAGGCCTG[A/G]CTGTGGAGAGCTCTC | 8078 |
rs781872446 | snp | C/T | 1.6501e-05 | 0.00287232 | synonymous-codon, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6857705 | CCACTTCGGCATCGA[C/T]ATGCTGAAGATGCAG | 8078 |
rs781872539 | in-del | -/C | 1.64844e-05 | 0.00287087 | intron-variant | USP5 | GRCh38.p7 | 12:6859444 | CAGGCCAGAGCCCCT[-/C]CAACTGTCCTTCCCT | 8078 |
rs781872815 | snp | A/T | 1.6473e-05 | 0.00286988 | missense, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6861023 | AAAAGATCAAGTGCC[A/T]GGCCACAGAGAAGGT | 8078 |
rs781873498 | snp | A/G | 1.64944e-05 | 0.00287175 | synonymous-codon, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6860217 | GGAGTCGGGCGATGG[A/G]GAGCGGGTGCCAGAA | 8078 |
rs781874072 | snp | A/G | 3.29745e-05 | 0.00406031 | missense | USP5 | GRCh38.p7 | 12:6865210 | GGGCACCTCTACCAT[A/G]TGTGGTCACTACGTC | 8078 |
rs781875338 | snp | C/T | | | intron-variant, downstream-variant-500B | USP5 | GRCh38.p7 | 12:6864374 | TGCTGGGTTTTTTGC[C/T]CCAGAACTTGTTAAA | 8078 |
rs781875743 | snp | C/T | | | upstream-variant-2KB, intron-variant | TPI1, USP5 | GRCh38.p7 | 12:6867107 | CGGGCATGAGCTGCT[C/T]CGATGGGCGAAGGAG | 8078 |
rs781876179 | snp | A/C | 6.70792e-05 | 0.00579095 | missense, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6856876 | AAGCTGGGCACCATC[A/C]CCCCTGATGGAGCTG | 8078 |
rs781876799 | snp | A/C | 1.72609e-05 | 0.00293771 | missense, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6858606 | CTTCAGCATCCCTGA[A/C]TTCCAGAGGAAGTGA | 8078 |
rs781878572 | snp | A/C | 1.65597e-05 | 0.00287743 | missense, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6856353 | GACTCAGCCTCCCGC[A/C]AGCAGGAGGTGCAGG | 8078 |
rs781879576 | snp | C/T | 1.65198e-05 | 0.00287395 | missense, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6858434 | CACAGACAGACAAGA[C/T]GATGACTGAGTTGGA | 8078 |
rs781885015 | snp | C/T | 1.76055e-05 | 0.00296689 | intron-variant | USP5 | GRCh38.p7 | 12:6856480 | CTCTGCCTCGGGCAC[C/T]ACCCCCAGAGCAAGG | 8078 |
rs781885522 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | USP5, CDCA3 | GRCh38.p7 | 12:6851314 | ACGCCCCCTGCCCTG[A/G]CCCTATTGGCTGAGC | 8078 |
rs781885670 | snp | A/T | | | intron-variant, upstream-variant-2KB | USP5, CDCA3 | GRCh38.p7 | 12:6853978 | TATTCCTGGAAGAGG[A/T]TGTCTGTTGTTGCTC | 8078 |
rs781886474 | snp | C/T | 1.64953e-05 | 0.00287182 | missense, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6860370 | ACTCTTCCCAGGAAG[C/T]TCAAGATGGCATTGC | 8078 |
rs781886575 | snp | C/T | 3.29489e-05 | 0.00405874 | upstream-variant-2KB, missense, utr-variant-5-prime, nc-transcript-variant | USP5, CDCA3 | GRCh38.p7 | 12:6850502 | GGTGTCCGTGCAATA[C/T]CAAGAGTAGGAGAGC | 8078 |
rs781888716 | snp | C/T | | | intron-variant | USP5 | GRCh38.p7 | 12:6857599 | GTCCTGAGCCACTTC[C/T]CCTGATTCTCTTCCT | 8078 |
rs781888910 | snp | A/G | | | upstream-variant-2KB, intron-variant | TPI1, USP5 | GRCh38.p7 | 12:6865759 | GCCTCCCTGGAATGG[A/G]TGGAGGGTGGTTGTA | 8078 |
rs781889403 | snp | C/G | 1.64868e-05 | 0.00287109 | synonymous-codon | USP5 | GRCh38.p7 | 12:6865201 | TAGTCACATGGGCAC[C/G]TCTACCATGTGTGGT | 8078 |
rs781890547 | snp | C/G | 1.64863e-05 | 0.00287104 | intron-variant | USP5 | GRCh38.p7 | 12:6859442 | CTCAGGCCAGAGCCC[C/G]TCCAACTGTCCTTCC | 8078 |
rs781891144 | snp | A/C | 1.69873e-05 | 0.00291434 | upstream-variant-2KB, intron-variant | USP5, CDCA3 | GRCh38.p7 | 12:6850787 | GGTTAGGAAGAGACC[A/C]AAGAATTCAGACATT | 8078 |
rs781891443 | snp | C/G | | | upstream-variant-2KB, intron-variant | TPI1, USP5 | GRCh38.p7 | 12:6867036 | GAACCCTGCATTTGT[C/G]CCGCAAGTTTTCACT | 8078 |
rs781892418 | snp | C/T | 1.70049e-05 | 0.00291585 | intron-variant | USP5 | GRCh38.p7 | 12:6864715 | TAATGCTTCCTTCCT[C/T]TCCAAGAACAATAGT | 8078 |
rs781892556 | snp | C/T | 4.94588e-05 | 0.00497262 | synonymous-codon, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6856719 | TAGTGGCTGGAAGTG[C/T]TCCAAGTGTGACATG | 8078 |
rs781893442 | snp | C/T | 1.66054e-05 | 0.00288139 | synonymous-codon, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6856337 | GGCCCTACTGTCGGC[C/T]GACTCAGCCTCCCGC | 8078 |
rs781894301 | snp | A/G | 1.65037e-05 | 0.00287256 | missense, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6856855 | ACAGGCTACCCGTTA[A/G]CTGTCAAGCTGGGCA | 8078 |
rs781894807 | snp | A/G | | | intron-variant | USP5 | GRCh38.p7 | 12:6860046 | TCTAAGGTTTTTCAC[A/G]TTGTTGAGAGTTAGC | 8078 |
rs781897206 | snp | C/G | | | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | USP5, CDCA3 | GRCh38.p7 | 12:6851909 | GCTGCAACCCCGAAG[C/G]CCACCTAGCTGCTCT | 8078 |
rs781897929 | snp | A/G | 3.36016e-05 | 0.00409874 | missense, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6863920 | TCTACTACACGGGCA[A/G]CAGCGGGGCTGAGGC | 8078 |
rs781898760 | snp | C/T | | | intron-variant | USP5 | GRCh38.p7 | 12:6856233 | AAGCACTGACAAAGC[C/T]GAAGGCCAAGGGGAA | 8078 |
rs781899290 | snp | C/T | 1.64768e-05 | 0.00287021 | intron-variant | USP5 | GRCh38.p7 | 12:6862429 | CAGGAGAGGAAAACC[C/T]TGGGGATTGTCTGGG | 8078 |
rs781900287 | snp | C/T | 3.29554e-05 | 0.00405914 | missense, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6861082 | ATGCAGCTGCCTGTG[C/T]CCATGGATGCAGCCC | 8078 |
rs781901040 | snp | A/G | 9.90786e-05 | 0.00703772 | synonymous-codon, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6855799 | AGACCCACCCCGGAA[A/G]AAGCCCACGCGGCTG | 8078 |
rs781902684 | snp | C/G | | | intron-variant, upstream-variant-2KB | USP5, CDCA3 | GRCh38.p7 | 12:6852721 | GCCGGGGTTGGAGTT[C/G]GGGGGTGGGGACCGC | 8078 |
rs781904013 | snp | A/G | | | intron-variant | USP5 | GRCh38.p7 | 12:6857467 | GTCAGCCCCAGAAGG[A/G]CCATGACCGCACTCA | 8078 |
rs781905351 | snp | A/G | | | intron-variant | USP5 | GRCh38.p7 | 12:6858277 | GAACTTGAACTGGAC[A/G]ATACTCAACATACCT | 8078 |
rs781905870 | snp | A/G | 1.67047e-05 | 0.00288999 | missense, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6861515 | TGCCAGAACTGGTTC[A/G]GGCCCAGGTGCCCTT | 8078 |
rs781910283 | in-del | -/T | 1.64751e-05 | 0.00287007 | upstream-variant-2KB, frameshift-variant, nc-transcript-variant | USP5, CDCA3 | GRCh38.p7 | 12:6850484 | CACTGCTGGTCTTCA[-/T]TAGGTGTCCGTGCAA | 8078 |
rs781912305 | snp | C/T | 1.65091e-05 | 0.00287303 | intron-variant | USP5 | GRCh38.p7 | 12:6857613 | CCCCTGATTCTCTTC[C/T]TGCCTCCTGCTCTAG | 8078 |
rs781912596 | snp | C/T | 1.65051e-05 | 0.00287267 | intron-variant | USP5 | GRCh38.p7 | 12:6859419 | GCTTCCTTCCCTTTT[C/T]CTCGGCGCTCAGGCC | 8078 |
rs781912741 | snp | A/C | | | intron-variant | USP5 | GRCh38.p7 | 12:6858766 | GCCCACACCCGTAAT[A/C]CCAGTACTTCGGGAG | 8078 |
rs781915951 | snp | C/G | 1.65318e-05 | 0.002875 | missense | USP5 | GRCh38.p7 | 12:6864849 | AGTCTGTGCCAGTGG[C/G]ACCTAAAGTCCGGGA | 8078 |
rs781916966 | snp | C/G | 1.67882e-05 | 0.00289721 | intron-variant | USP5 | GRCh38.p7 | 12:6856301 | GACCCTCTGCTTCCC[C/G]CAGGTGACCAGTGCA | 8078 |
rs781917894 | snp | G/T | 1.80146e-05 | 0.00300116 | intron-variant, downstream-variant-500B | USP5 | GRCh38.p7 | 12:6864243 | AGTGGGGAAGAAGGG[G/T]GTGGGAATGAGGGGC | 8078 |
rs781918867 | snp | C/T | | | intron-variant | USP5 | GRCh38.p7 | 12:6863508 | GCCCTCTTTGATTGA[C/T]ATGGGGCCTCCCCAG | 8078 |
rs781920743 | snp | A/G/T | 5.40208e-05 | 0.00519692 | intron-variant | USP5 | GRCh38.p7 | 12:6863794 | GCAAACAGTGGCCCA[A/G/T]TCAGTCGGTCCGTGT | 8078 |
rs781921685 | snp | C/T | | | intron-variant | USP5 | GRCh38.p7 | 12:6857844 | CCCATCCCCAAGATA[C/T]ACAGGCTTCTTTTAA | 8078 |
rs781922758 | snp | C/T | 1.66813e-05 | 0.00288797 | missense, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6864163 | TCCATGGGCTTCTCC[C/T]GGGACCAGGCCTTGA | 8078 |
rs781924172 | snp | C/T | 1.64754e-05 | 0.00287009 | synonymous-codon, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6856797 | GCGACGCTACTTCGA[C/T]GGCAGTGGGGGCAAC | 8078 |
rs781924594 | snp | C/T | 1.66571e-05 | 0.00288587 | intron-variant | USP5 | GRCh38.p7 | 12:6865144 | TGTTTCCTTCTCTGA[C/T]CCCCTCTCTCCTTTC | 8078 |
rs781925367 | snp | A/G | 1.64792e-05 | 0.00287042 | upstream-variant-2KB, intron-variant | USP5, CDCA3 | GRCh38.p7 | 12:6850459 | CATTCCCTGGGCCCA[A/G]CGCTTACCTCCACTG | 8078 |
rs781925982 | snp | C/T | | | intron-variant | USP5 | GRCh38.p7 | 12:6859726 | GGCGCGATCTCGGCT[C/T]ACTACAACCTCTGCC | 8078 |
rs781927873 | snp | A/G | 3.29489e-05 | 0.00405874 | missense, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6856122 | CCCGGGATGGACTGG[A/G]GGGACTGCCTGACAT | 8078 |
rs781928247 | snp | A/T | 3.07924e-05 | 0.00392368 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | USP5, CDCA3 | GRCh38.p7 | 12:6852156 | GTGGGAGCCGCCGTG[A/T]GTGGAGAAGCTGCTG | 8078 |
rs781928783 | snp | A/G | 1.64751e-05 | 0.00287007 | upstream-variant-2KB, missense, utr-variant-5-prime, nc-transcript-variant | USP5, CDCA3 | GRCh38.p7 | 12:6850494 | TCTTCATAGGTGTCC[A/G]TGCAATACCAAGAGT | 8078 |
rs781929940 | snp | C/T | | | upstream-variant-2KB, intron-variant | TPI1, USP5 | GRCh38.p7 | 12:6866763 | TCACTGGTTCTAGAG[C/T]TCTAGGAAAATTGGG | 8078 |
rs781931263 | snp | A/G/T | 0.00013248 | 0.0081378 | intron-variant | USP5 | GRCh38.p7 | 12:6855712 | CCGACTTGTTCCTTC[A/G/T]CTCGTGCTCATTGCT | 8078 |
rs781932638 | snp | C/T | 5.08229e-05 | 0.00504072 | intron-variant | USP5 | GRCh38.p7 | 12:6863393 | GTTAGTGACTCTTCT[C/T]CCTGCCTGTCTCTCT | 8078 |
rs781933877 | snp | G/T | 4.50694e-05 | 0.00474686 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | USP5, CDCA3 | GRCh38.p7 | 12:6852191 | TGTCATGGCGGAGCT[G/T]AGTGAGGAGGCGCTG | 8078 |
rs781934544 | snp | A/G | 1.64936e-05 | 0.00287168 | intron-variant | USP5 | GRCh38.p7 | 12:6860124 | TTAGTTGACTGAAGT[A/G]AAATGTTTTCTTGGA | 8078 |
rs781935177 | snp | G/T | 1.68957e-05 | 0.00290647 | intron-variant | USP5 | GRCh38.p7 | 12:6858381 | AGGTAAAAACTACAG[G/T]GTTGAGTTTCTCACT | 8078 |
rs781936322 | snp | A/G | 0.000224986 | 0.0106039 | missense, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6861473 | ACGAGGAGAAGAAGC[A/G]GCAAGCCGAAGAGGA | 8078 |
rs781936435 | snp | C/T | 0.000147216 | 0.00857824 | intron-variant | USP5 | GRCh38.p7 | 12:6861632 | AGTAAGTCCTCTGGT[C/T]GGGGCCTGAGGCTGT | 8078 |
rs781936880 | in-del | -/C | 0.00028166 | 0.0118638 | upstream-variant-2KB, intron-variant | TPI1, USP5 | GRCh38.p7 | 12:6865957 | GCCCAGTTTGTTCAT[-/C]CTTTTCTGTTTTCCC | 8078 |
rs781937102 | snp | A/G | | | upstream-variant-2KB, intron-variant | TPI1, USP5 | GRCh38.p7 | 12:6865915 | CCAGGGGCCATGTCT[A/G]AGAGACTACATGATG | 8078 |
rs781937193 | snp | A/G | | | intron-variant | USP5 | GRCh38.p7 | 12:6856501 | CAGAGCAAGGACAAG[A/G]AGCCCACTTTTCTGG | 8078 |
rs781942316 | snp | A/G | 6.60611e-05 | 0.00574684 | intron-variant | USP5 | GRCh38.p7 | 12:6860277 | TCAGGCCCTGGGATT[A/G]TGGGGAAGCTGAGGT | 8078 |
rs781943412 | snp | A/G | | | upstream-variant-2KB, synonymous-codon, intron-variant, nc-transcript-variant | USP5, CDCA3 | GRCh38.p7 | 12:6850941 | GACTGGGACGCTCTT[A/G]GCTGAGCCCATCTCA | 8078 |
rs781944122 | snp | G/T | | | intron-variant, downstream-variant-500B | USP5 | GRCh38.p7 | 12:6864290 | GACCAAAGACAACAG[G/T]TGTGGTCTGGCCGAG | 8078 |
rs781945074 | in-del | -/A | 0.000141485 | 0.00840967 | intron-variant, downstream-variant-500B | USP5 | GRCh38.p7 | 12:6864692 | AGACTCCGTCTCAAG[-/A]AAAAAAGTAATGCTT | 8078 |
rs781945300 | snp | A/T | | | intron-variant | USP5 | GRCh38.p7 | 12:6855120 | GCAGGTGGAAAGATA[A/T]ATGGTGACTGGTGTT | 8078 |
rs781946029 | snp | G/T | 1.67995e-05 | 0.00289819 | missense, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6856425 | AGCCTCAAGCAGTTG[G/T]ACAACCCTGCTCGAA | 8078 |
rs781947549 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP5, CDCA3 | GRCh38.p7 | 12:6852844 | AGGGGGCGGGGAGGG[A/G]AGGAAAGAGGAGAGG | 8078 |
rs781949698 | snp | C/T | | | intron-variant | USP5 | GRCh38.p7 | 12:6859686 | TGAGACGGAGTCTTG[C/T]TCTGTTGCCAGGCTG | 8078 |
rs781950021 | snp | A/G | 1.64787e-05 | 0.00287038 | missense, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6860963 | CATAGAGGAATTGCC[A/G]GAGCTCTGAAAATCC | 8078 |
rs781951093 | snp | A/G | 1.64925e-05 | 0.00287158 | missense, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6856847 | ACCGAGAGACAGGCT[A/G]CCCGTTAGCTGTCAA | 8078 |
rs781952541 | snp | A/G | | | intron-variant | USP5 | GRCh38.p7 | 12:6857278 | TCCAGCCTGGGCTAC[A/G]GAGACCCTGTCTCAA | 8078 |
rs781953121 | snp | A/G | | | upstream-variant-2KB, missense, utr-variant-5-prime, nc-transcript-variant | USP5, CDCA3 | GRCh38.p7 | 12:6850499 | ATAGGTGTCCGTGCA[A/G]TACCAAGAGTAGGAG | 8078 |
rs781953596 | snp | A/G | 1.64977e-05 | 0.00287203 | intron-variant | USP5 | GRCh38.p7 | 12:6856700 | GATTCTCTTCTCTGT[A/G]GGTTAGTGGCTGGAA | 8078 |
rs781953874 | snp | C/T | 1.64895e-05 | 0.00287132 | synonymous-codon, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6855472 | GTATGTGGAGAGACA[C/T]TTCAATAAGACCGGC | 8078 |
rs781956020 | snp | C/T | 3.35644e-05 | 0.00409647 | intron-variant | USP5 | GRCh38.p7 | 12:6864905 | GAAGCAGGACAGGCC[C/T]GGTGGAATCTGGTCA | 8078 |
rs781956555 | snp | C/T | | | upstream-variant-2KB, intron-variant | TPI1, USP5 | GRCh38.p7 | 12:6865816 | ATAGGGTCCGTGACC[C/T]TTGTGAGGTTGTGAA | 8078 |
rs781956915 | snp | C/T | 1.68758e-05 | 0.00290476 | missense, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6864068 | TTGCAAACCCCCTCA[C/T]CCTGCCTGGCTCTAG | 8078 |
rs781957346 | snp | C/T | 1.64743e-05 | 0.00287 | synonymous-codon, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6856039 | AGGCGGATTTGACCT[C/T]AGCGAGGAGAAGTTT | 8078 |
rs781962055 | snp | C/G | 1.65512e-05 | 0.00287669 | intron-variant | USP5 | GRCh38.p7 | 12:6857752 | CAACTTCAGATTCTT[C/G]TACTTCCTGCCCCTG | 8078 |
rs781963616 | snp | C/T | | | intron-variant | USP5 | GRCh38.p7 | 12:6857089 | CTAGGAGTTCGAGAC[C/T]AGCCTGGGCAACATA | 8078 |
rs781963847 | snp | A/T | | | upstream-variant-2KB, intron-variant | TPI1, USP5 | GRCh38.p7 | 12:6866647 | ATTGTGTCCTGTTTG[A/T]TACCTTGGGGGAGAG | 8078 |
rs781963937 | snp | C/T | 7.97035e-05 | 0.00631232 | upstream-variant-2KB, utr-variant-5-prime, intron-variant, nc-transcript-variant | USP5, CDCA3 | GRCh38.p7 | 12:6850991 | GGGCAAGGGCCAGCC[C/T]GGGACGAGGAGGGAA | 8078 |
rs781964611 | snp | C/G | 1.67253e-05 | 0.00289178 | missense, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6861508 | ATGGCACTGCCAGAA[C/G]TGGTTCGGGCCCAGG | 8078 |
rs781965141 | snp | A/G | | | intron-variant | USP5 | GRCh38.p7 | 12:6859275 | CCTCTGCCGCCGAGC[A/G]TGCTTGCACATTGGA | 8078 |
rs781966768 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP5, CDCA3 | GRCh38.p7 | 12:6852365 | CGCTGGGGCCTGCAA[A/G]GCTTGGGCTACCGCC | 8078 |
rs781966860 | snp | C/G | | | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | USP5, CDCA3 | GRCh38.p7 | 12:6851438 | GTCAATGGACTGATG[C/G]TAGGCTTGCCCAGGG | 8078 |
rs781967034 | snp | C/T | 3.29799e-05 | 0.00406065 | intron-variant | USP5 | GRCh38.p7 | 12:6860347 | GCCCCAGCTGAGTCC[C/T]TGCCCTGACTCTTCC | 8078 |
rs781969412 | snp | A/G | | | intron-variant | USP5 | GRCh38.p7 | 12:6861362 | AGGAACTGAAATACG[A/G]ACACAGAGCCAGTAG | 8078 |
rs781970895 | snp | A/C/G | 3.31166e-05 | 0.00406908 | intron-variant | USP5 | GRCh38.p7 | 12:6861149 | GCACGGTGGGAGGCT[A/C/G]AGGTCTAGGAGGAAT | 8078 |
rs781975000 | snp | C/T | 1.6501e-05 | 0.00287232 | intron-variant | USP5 | GRCh38.p7 | 12:6859429 | CTTTTCCTCGGCGCT[C/T]AGGCCAGAGCCCCTC | 8078 |
rs781978168 | snp | C/G | | | upstream-variant-2KB, intron-variant | USP5, CDCA3 | GRCh38.p7 | 12:6850204 | TGTATTTTTTCTAGA[C/G]ATGGGGTTTTGCCAT | 8078 |
rs781980130 | snp | A/G | 3.29625e-05 | 0.00405958 | upstream-variant-2KB, intron-variant | USP5, CDCA3 | GRCh38.p7 | 12:6850615 | TCAAGACCATAGGCT[A/G]GAACAAGTCTGGGCC | 8078 |
rs781981110 | snp | A/C | 6.60895e-05 | 0.00574808 | intron-variant | USP5 | GRCh38.p7 | 12:6857730 | ATGCAGAAGGTGAGA[A/C]CCCCTTCAACTTCAG | 8078 |
rs781982046 | snp | C/G | 0.000250023 | 0.0111781 | intron-variant | USP5 | GRCh38.p7 | 12:6860516 | GGCAAGATGGCACAC[C/G]CCCATCTTCCTGCAA | 8078 |
rs781982316 | snp | C/G | | | intron-variant, downstream-variant-500B | USP5 | GRCh38.p7 | 12:6864559 | CCAAGCGTGGTGGTG[C/G]GCGTCTGTAGTCCCA | 8078 |
rs781982540 | snp | A/G | | | intron-variant | USP5 | GRCh38.p7 | 12:6854740 | TCCAGCCTGGGTGAC[A/G]GAGTGCAGTGTCTCT | 8078 |
rs781983695 | snp | A/C/T | 4.93039e-05 | 0.00496487 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | USP5, CDCA3 | GRCh38.p7 | 12:6852179 | AGCTGCTGCCGGTGT[A/C/T]ATGGCGGAGCTGAGT | 8078 |
rs781983707 | snp | C/T | 1.65397e-05 | 0.00287569 | stop-gained, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6863224 | GAGCTCGACATCTCC[C/T]AGTTGAGGGGCACAG | 8078 |
rs781985017 | snp | C/T | | | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | USP5, CDCA3 | GRCh38.p7 | 12:6851629 | CAGCTGGAGTTGTGA[C/T]GGTTTTCCTGAGGCG | 8078 |
rs781985729 | snp | C/T | 1.64909e-05 | 0.00287144 | intron-variant | USP5 | GRCh38.p7 | 12:6860318 | TCTAAAGAAGGCCCC[C/T]GGATGGCCACTGAGC | 8078 |
rs781985947 | snp | C/G/T | 0.000100857 | 0.0071007 | intron-variant, upstream-variant-2KB | USP5, CDCA3 | GRCh38.p7 | 12:6852316 | TCCCCACGCCCGCAA[C/G/T]GAGCACGACTTCCTT | 8078 |
rs781989398 | snp | C/T | 1.65236e-05 | 0.00287429 | synonymous-codon, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6855766 | ACAGAAAGAGGAGGA[C/T]CCTGCTACAGGCACT | 8078 |
rs781991611 | snp | G/T | | | intron-variant | USP5 | GRCh38.p7 | 12:6862690 | TCAATGTTTCAAAAT[G/T]TATCTAGTTTGAAAG | 8078 |
rs781992273 | in-del | -/G | | | intron-variant, upstream-variant-2KB | USP5, CDCA3 | GRCh38.p7 | 12:6852449 | CCTTTCATTAACTGC[-/G]GCTGTCGTGTGACTA | 8078 |
rs781993259 | snp | A/C | 1.64863e-05 | 0.00287104 | missense, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6862553 | ACTGGGTGCCCAAGA[A/C]ACTGGGTATGGCTGC | 8078 |
rs781994245 | snp | A/G | 1.65266e-05 | 0.00287455 | intron-variant | USP5 | GRCh38.p7 | 12:6865281 | GCGTTTTGAATGGAG[A/G]ATGGTGGTGGGAATG | 8078 |
rs781995747 | snp | C/T | 1.67276e-05 | 0.00289197 | upstream-variant-2KB, utr-variant-3-prime | TPI1, USP5 | GRCh38.p7 | 12:6866118 | AGGGCAGGGGAAGAC[C/T]ACCTGGCATGAGGGA | 8078 |
rs781997401 | snp | C/G | | | intron-variant | USP5 | GRCh38.p7 | 12:6856525 | TTTCTGGGGGATCTG[C/G]TGGGAGAGAGGGTAG | 8078 |
rs781997483 | snp | A/C | 1.65384e-05 | 0.00287557 | intron-variant | USP5 | GRCh38.p7 | 12:6857586 | GGTGGCCTGGCTAGT[A/C]CTGAGCCACTTCCCC | 8078 |
rs781997530 | snp | C/T | | | intron-variant | USP5 | GRCh38.p7 | 12:6859380 | CTCTTGAGGGGAGCC[C/T]GTTCACAGAGTTAGT | 8078 |
rs781998201 | snp | A/G | 3.31686e-05 | 0.00407225 | synonymous-codon, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6856400 | ACGGCAGGTGTCTAA[A/G]CATGCCTTCAGCCTC | 8078 |
rs782000287 | snp | A/G | 3.72738e-05 | 0.00431689 | intron-variant | USP5 | GRCh38.p7 | 12:6861641 | TCTGGTCGGGGCCTG[A/G]GGCTGTGGGTCTATG | 8078 |
rs782002031 | snp | C/G | 1.95257e-05 | 0.0031245 | upstream-variant-2KB, utr-variant-5-prime, intron-variant, nc-transcript-variant | USP5, CDCA3 | GRCh38.p7 | 12:6850984 | AGGGTGGGGGCAAGG[C/G]CCAGCCCGGGACGAG | 8078 |
rs782006550 | snp | A/G | | | intron-variant | USP5 | GRCh38.p7 | 12:6859324 | AACAGGCAGGTTGCT[A/G]GAGAGAAGCGACTCC | 8078 |
rs782008995 | snp | A/G | | | intron-variant | USP5 | GRCh38.p7 | 12:6854989 | TTGAATGTAATCTCC[A/G]GCACTGGAAGTCCAC | 8078 |
rs782009387 | snp | C/T | 1.64757e-05 | 0.00287012 | upstream-variant-2KB, missense, nc-transcript-variant | USP5, CDCA3 | GRCh38.p7 | 12:6850476 | GCTTACCTCCACTGC[C/T]GGTCTTCATAGGTGT | 8078 |
rs782009475 | snp | C/T | 1.69003e-05 | 0.00290687 | intron-variant | USP5 | GRCh38.p7 | 12:6865128 | TCAAGCATTCCTCTT[C/T]TGTTTCCTTCTCTGA | 8078 |
rs782013369 | snp | C/G | 2.04055e-05 | 0.00319411 | upstream-variant-2KB, utr-variant-5-prime, intron-variant, nc-transcript-variant | USP5, CDCA3 | GRCh38.p7 | 12:6850997 | GGGCCAGCCCGGGAC[C/G]AGGAGGGAATGCCTG | 8078 |
rs782013738 | snp | G/T | 1.66638e-05 | 0.00288645 | synonymous-codon | USP5 | GRCh38.p7 | 12:6864739 | CAATAGTTTAGAACG[G/T]GCTGTGGACTGGATC | 8078 |
rs782013983 | snp | C/G | 3.29712e-05 | 0.00406011 | missense, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6863252 | CAGGGCTGCAGCCCG[C/G]AGAGGAGGAGCTGCC | 8078 |
rs782014206 | snp | A/G | | | intron-variant | USP5 | GRCh38.p7 | 12:6859756 | CTCCTGGGTTCAAGT[A/G]ATTCTCCTGCCTCAG | 8078 |
rs782015664 | snp | A/C | | | intron-variant | USP5 | GRCh38.p7 | 12:6860679 | CCCTTGATGGGCTTG[A/C]AGCCCAATTCAGATT | 8078 |
rs782019559 | snp | C/T | 1.66776e-05 | 0.00288765 | intron-variant | USP5 | GRCh38.p7 | 12:6855556 | GGGGCAAGGCCTGGG[C/T]ACATTGTCTGTTCCA | 8078 |
rs782020937 | snp | C/T | 1.65408e-05 | 0.00287578 | synonymous-codon, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6858558 | CCGGAACCTGGGTAA[C/T]AGCTGCTACCTCAAC | 8078 |
rs782021481 | snp | A/G | 1.66871e-05 | 0.00288847 | missense, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6856320 | GTGACCAGTGCAGTG[A/G]AGGCCCTACTGTCGG | 8078 |
rs782022808 | snp | C/T | 1.68004e-05 | 0.00289826 | synonymous-codon, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6863888 | GGGATTCCCTATGGA[C/T]GCCTGCCGCAAAGCT | 8078 |
rs782024209 | snp | A/G | | | intron-variant | USP5 | GRCh38.p7 | 12:6865380 | AAAGTGCCAGAGAGT[A/G]ACAGAAGGTCTTGCA | 8078 |
rs782024660 | snp | C/T | 1.64901e-05 | 0.00287137 | missense, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6860201 | ATTCCAAGCCAGTAC[C/T]GGAGTCGGGCGATGG | 8078 |
rs782028656 | snp | A/G | 1.64852e-05 | 0.00287094 | missense, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6862550 | TAGACTGGGTGCCCA[A/G]GAAACTGGGTATGGC | 8078 |
rs782029302 | snp | C/T | 3.30087e-05 | 0.00406242 | intron-variant | USP5 | GRCh38.p7 | 12:6859425 | TTCCCTTTTCCTCGG[C/T]GCTCAGGCCAGAGCC | 8078 |
rs782030458 | snp | C/T | 1.65375e-05 | 0.0028755 | intron-variant, upstream-variant-2KB | USP5, CDCA3 | GRCh38.p7 | 12:6852310 | GCCCATTCCCCACGC[C/T]CGCAACGAGCACGAC | 8078 |
rs782031903 | snp | A/G | 0.000266991 | 0.011551 | synonymous-codon, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6856319 | GGTGACCAGTGCAGT[A/G]GAGGCCCTACTGTCG | 8078 |
rs782034838 | snp | C/G | 3.38146e-05 | 0.00411171 | upstream-variant-2KB, missense, intron-variant, nc-transcript-variant | USP5, CDCA3 | GRCh38.p7 | 12:6850861 | CGCAGGATGCCAGCA[C/G]TAGGTGAACGGGGGT | 8078 |
rs782035473 | snp | A/G | 6.72179e-05 | 0.00579693 | upstream-variant-2KB, utr-variant-3-prime | TPI1, USP5 | GRCh38.p7 | 12:6866124 | GGGGAAGACCACCTG[A/G]CATGAGGGAGAGGGG | 8078 |
rs782036420 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP5, CDCA3 | GRCh38.p7 | 12:6853259 | AACCAGCTCATGGCC[C/T]GAAAACTGCAAGTCA | 8078 |
rs782036728 | snp | C/T | | | intron-variant | USP5 | GRCh38.p7 | 12:6862399 | CATGAGGGGCTGAAC[C/T]CCAGGTGGGAGTTTC | 8078 |
rs782038051 | snp | C/G | | | intron-variant, downstream-variant-500B | USP5 | GRCh38.p7 | 12:6864576 | CGTCTGTAGTCCCAG[C/G]TACTTGGGAGGCTGA | 8078 |
rs782038751 | snp | C/T | 1.64855e-05 | 0.00287097 | synonymous-codon, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6856141 | ACTGCCTGACATTGT[C/T]AGAGATCGGGTATGA | 8078 |
rs782039343 | snp | A/G | | | intron-variant | USP5 | GRCh38.p7 | 12:6856628 | TTGGATTGGCGGGGG[A/G]CCTGCAGAGCCCTCT | 8078 |
rs782039989 | snp | A/G | 1.6604e-05 | 0.00288127 | missense | USP5 | GRCh38.p7 | 12:6864875 | CGGGATGGTCCTGGA[A/G]GTGAGTATCCCCAGG | 8078 |
rs782043036 | snp | A/C | 4.9423e-05 | 0.00497082 | upstream-variant-2KB, missense, utr-variant-5-prime, nc-transcript-variant | USP5, CDCA3 | GRCh38.p7 | 12:6850498 | CATAGGTGTCCGTGC[A/C]ATACCAAGAGTAGGA | 8078 |
rs782044089 | snp | C/T | | | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | USP5, CDCA3 | GRCh38.p7 | 12:6851269 | GCTCGTGGCTCAACT[C/T]CCGAAGTTACCAGTT | 8078 |
rs782044155 | snp | C/T | 1.64909e-05 | 0.00287144 | intron-variant | USP5 | GRCh38.p7 | 12:6860357 | AGTCCCTGCCCTGAC[C/T]CTTCCCAGGAAGTTC | 8078 |
rs782045182 | snp | C/T | | | intron-variant | USP5 | GRCh38.p7 | 12:6857540 | GCTCTCCTTCTGTCC[C/T]CTCAAGTCCCTTCTG | 8078 |
rs782049665 | snp | A/C | 1.66515e-05 | 0.00288539 | intron-variant | USP5 | GRCh38.p7 | 12:6855539 | CCGGTAGGAGCAGGG[A/C]TGGGGCAAGGCCTGG | 8078 |
rs782050914 | snp | C/T | | | intron-variant | USP5 | GRCh38.p7 | 12:6859692 | GGAGTCTTGTTCTGT[C/T]GCCAGGCTGGAGTGC | 8078 |
rs782051229 | snp | C/T | 1.64985e-05 | 0.0028721 | upstream-variant-2KB, intron-variant | USP5, CDCA3 | GRCh38.p7 | 12:6850644 | CCCTGACTCTTCTCT[C/T]CTCTCCTCCCCATAT | 8078 |
rs782054267 | snp | C/T | | | intron-variant | USP5 | GRCh38.p7 | 12:6860562 | TCCTGCCCATTTCTC[C/T]CTCTATCAGCCCCAA | 8078 |
rs782054758 | snp | A/G | | | upstream-variant-2KB, intron-variant | TPI1, USP5 | GRCh38.p7 | 12:6866961 | CAGGCCTTGCCAGCC[A/G]GGGCGAGGGTTGGGA | 8078 |
rs782055134 | snp | G/T | | | intron-variant, upstream-variant-2KB | USP5, CDCA3 | GRCh38.p7 | 12:6853371 | ATTTGTGGTTTGCTT[G/T]GTTTGCTAGGCTTTG | 8078 |
rs782055658 | snp | A/G | | | intron-variant, downstream-variant-500B | USP5 | GRCh38.p7 | 12:6864668 | CACTCCAGCCTGGGC[A/G]ACAGAGCAAGACTCC | 8078 |
rs782056096 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP5, CDCA3 | GRCh38.p7 | 12:6852787 | TCAAGAAGTCCGATT[C/T]TGAGAAAGGCAGAGA | 8078 |
rs782056306 | snp | C/T | 4.99247e-05 | 0.00499598 | intron-variant | USP5 | GRCh38.p7 | 12:6865145 | GTTTCCTTCTCTGAC[C/T]CCCTCTCTCCTTTCC | 8078 |
rs782058077 | snp | C/T | 1.64792e-05 | 0.00287042 | synonymous-codon, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6862530 | CAAGAAGTTCACCTT[C/T]GGCTTAGACTGGGTG | 8078 |
rs782059307 | snp | A/G | 1.78372e-05 | 0.00298635 | intron-variant, downstream-variant-500B | USP5 | GRCh38.p7 | 12:6864674 | AGCCTGGGCGACAGA[A/G]CAAGACTCCGTCTCA | 8078 |
rs782062279 | snp | C/T | | | intron-variant | USP5 | GRCh38.p7 | 12:6859911 | CTGCCCACCTCGGCC[C/T]CCCAAAGTGCTGGGA | 8078 |
rs782065035 | snp | A/G | | | intron-variant, downstream-variant-500B | USP5 | GRCh38.p7 | 12:6864644 | CAGTGAGCCGAGATC[A/G]CGCCACTGCACTCCA | 8078 |
rs782065985 | snp | C/T | | | intron-variant | USP5 | GRCh38.p7 | 12:6862748 | TTTGATTGTTATAGG[C/T]ATGATTTACAACCAA | 8078 |
rs782066186 | snp | A/C/G | 0.000335848 | 0.0129546 | synonymous-codon, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6863915 | AGCTGTCTACTACAC[A/C/G]GGCAACAGCGGGGCT | 8078 |
rs782066589 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP5, CDCA3 | GRCh38.p7 | 12:6853137 | TGTCACCCTCAAGCG[A/G]AGGCCCTTTGGGGCC | 8078 |
rs782069015 | snp | G/T | 6.58903e-05 | 0.00573941 | missense, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6859488 | TGTGGATAAGCTGGA[G/T]AAGATCTTCCAGAAT | 8078 |
rs782069794 | snp | A/G | | | intron-variant | USP5 | GRCh38.p7 | 12:6861892 | CATTGCCCCTCAGTC[A/G]TGGCTGAGCACAGGC | 8078 |
rs782070238 | snp | A/G/T | 3.34823e-05 | 0.00409146 | missense, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6863896 | CTATGGACGCCTGCC[A/G/T]CAAAGCTGTCTACTA | 8078 |
rs782071221 | snp | A/G | | | intron-variant | USP5 | GRCh38.p7 | 12:6855256 | AGGTCCTAAAAGGCT[A/G]AATAACTTGCCAAGG | 8078 |
rs782074141 | snp | C/G | 1.92795e-05 | 0.00310474 | intron-variant | USP5 | GRCh38.p7 | 12:6861662 | TGGGTCTATGGCAGA[C/G]CTATCCCAGAGGATA | 8078 |
rs782075805 | snp | C/T | | | intron-variant | USP5 | GRCh38.p7 | 12:6858096 | GCCTAGTTTAGGGAT[C/T]AGGGACATTTCCCTG | 8078 |
rs782076301 | snp | C/T | | | intron-variant | USP5 | GRCh38.p7 | 12:6857426 | TAATTCCAACCCTCA[C/T]CCGGTTTCATCTGTC | 8078 |
rs782076351 | snp | A/T | 1.65946e-05 | 0.00288046 | missense, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6856403 | GCAGGTGTCTAAGCA[A/T]GCCTTCAGCCTCAAG | 8078 |
rs782078808 | snp | A/G | 6.59598e-05 | 0.00574243 | intron-variant | USP5 | GRCh38.p7 | 12:6860327 | GGCCCCTGGATGGCC[A/G]CTGAGCCCCAGCTGA | 8078 |
rs782080084 | snp | C/G | | | intron-variant, upstream-variant-2KB | USP5, CDCA3 | GRCh38.p7 | 12:6852478 | TACCGTCCCCGGAAG[C/G]CGCCGCGCTCACCTC | 8078 |
rs782080206 | snp | A/G | 1.65222e-05 | 0.00287417 | missense, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6855492 | ATAAGACCGGCCAGC[A/G]AGTCTACTTGCACCT | 8078 |
rs782080851 | snp | C/T | 0.000115931 | 0.00761264 | synonymous-codon | USP5 | GRCh38.p7 | 12:6864763 | CTGGATCTTCAGTCA[C/T]ATTGACGACCTGGAT | 8078 |
rs782081648 | snp | A/G | 1.65499e-05 | 0.00287657 | intron-variant | USP5 | GRCh38.p7 | 12:6865294 | AGAATGGTGGTGGGA[A/G]TGAGGAGGGCCATTT | 8078 |
rs782081898 | in-del | -/G | | | upstream-variant-2KB, intron-variant | TPI1, USP5 | GRCh38.p7 | 12:6865559 | TGAGCTACCGTGCCT[-/G]GCCAGGCCCCCTGCC | 8078 |
rs782082104 | snp | C/T | 1.6473e-05 | 0.00286988 | synonymous-codon, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6861045 | AGAGAAGGTGAAGTA[C/T]ACCCAGCGAGTTGAC | 8078 |
rs782087021 | snp | A/G | | | intron-variant | USP5 | GRCh38.p7 | 12:6859893 | ATCTCCTGACCTCGT[A/G]GTCTGCCCACCTCGG | 8078 |
rs782087757 | snp | C/T | 1.6492e-05 | 0.00287154 | synonymous-codon, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6856848 | CCGAGAGACAGGCTA[C/T]CCGTTAGCTGTCAAG | 8078 |
rs782088031 | snp | A/G | 3.47084e-05 | 0.00416569 | intron-variant | USP5 | GRCh38.p7 | 12:6863421 | TCTCCCGTGCTGATG[A/G]GGGCCTCTCTGCCTT | 8078 |
rs782088853 | snp | A/C/G | | | intron-variant | USP5 | GRCh38.p7 | 12:6857353 | CACTCAAATCCTCAT[A/C/G]CCTTTCCTACCAAGC | 8078 |
rs782095332 | snp | C/T | 1.66233e-05 | 0.00288295 | missense, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6856333 | TGGAGGCCCTACTGT[C/T]GGCCGACTCAGCCTC | 8078 |
rs782096199 | snp | C/T | | | intron-variant, downstream-variant-500B | USP5 | GRCh38.p7 | 12:6864427 | GGGCGCGGTGGCTCA[C/T]GCCTGTAATCCCAGC | 8078 |
rs782096600 | snp | A/G | 9.88484e-05 | 0.00702954 | intron-variant | USP5 | GRCh38.p7 | 12:6859561 | GTAACCAGGTCCTAT[A/G]TAGGAAAGCTGTTGA | 8078 |
rs782097739 | snp | C/T | 1.65091e-05 | 0.00287303 | intron-variant | USP5 | GRCh38.p7 | 12:6856163 | CGGGTATGACTGCCC[C/T]CTATGCTACCCAAGA | 8078 |
rs782098205 | snp | C/T | 3.29658e-05 | 0.00405978 | upstream-variant-2KB, intron-variant | USP5, CDCA3 | GRCh38.p7 | 12:6850619 | GACCATAGGCTAGAA[C/T]AAGTCTGGGCCCTGA | 8078 |
rs782099215 | snp | A/G | 1.66966e-05 | 0.00288929 | missense, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6864082 | ATCCTGCCTGGCTCT[A/G]GTGGGCCGGGCTCCA | 8078 |
rs782099266 | snp | C/T | | | intron-variant | USP5 | GRCh38.p7 | 12:6858962 | CACAAACCCCACTGA[C/T]AGTGCAGAGTGCCAA | 8078 |
rs782099616 | snp | A/G | | | intron-variant | USP5 | GRCh38.p7 | 12:6865321 | ATTTGGAAGTCCTTG[A/G]GATAGCTATGGGAGA | 8078 |
rs782100478 | snp | A/T | | | intron-variant | USP5 | GRCh38.p7 | 12:6859053 | GGCAGTGACATCAGA[A/T]GAGCACCTAACATGG | 8078 |
rs782100584 | snp | C/T | 1.64931e-05 | 0.00287163 | synonymous-codon | USP5 | GRCh38.p7 | 12:6865180 | GTATCAGCTCTTTGC[C/T]TTCATTAGTCACATG | 8078 |
rs782100814 | snp | C/T | | | intron-variant | USP5 | GRCh38.p7 | 12:6862040 | CAGCTACCCAGCCCT[C/T]TGCTGCTCCTGCCAG | 8078 |
rs782101225 | snp | A/G | | | upstream-variant-2KB, intron-variant | TPI1, USP5 | GRCh38.p7 | 12:6867109 | GGCATGAGCTGCTCC[A/G]ATGGGCGAAGGAGGT | 8078 |
rs782102175 | snp | G/T | 1.64969e-05 | 0.00287196 | intron-variant | USP5 | GRCh38.p7 | 12:6856702 | TTCTCTTCTCTGTGG[G/T]TTAGTGGCTGGAAGT | 8078 |
rs782102759 | snp | C/G | 1.65239e-05 | 0.00287431 | missense, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6855770 | AAAGAGGAGGACCCT[C/G]CTACAGGCACTGGAG | 8078 |
rs782102900 | snp | C/T | | | intron-variant | USP5 | GRCh38.p7 | 12:6862739 | AAAGACTTCTTTGAT[C/T]GTTATAGGTATGATT | 8078 |
rs782103156 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | USP5, CDCA3 | GRCh38.p7 | 12:6851818 | CTAAAACAACCGTCA[A/G]TTCCTGCTCTTCAAT | 8078 |
rs782105364 | snp | A/G | 3.3592e-05 | 0.00409815 | intron-variant | USP5 | GRCh38.p7 | 12:6864909 | CAGGACAGGCCTGGT[A/G]GAATCTGGTCAGTCT | 8078 |
rs782105541 | snp | A/C | | | intron-variant | USP5 | GRCh38.p7 | 12:6861996 | GGCATGGGTGTGAGA[A/C]CTGAAAAAGGGCTTT | 8078 |
rs782106191 | snp | C/T | 1.70382e-05 | 0.0029187 | upstream-variant-2KB, synonymous-codon, intron-variant, nc-transcript-variant | USP5, CDCA3 | GRCh38.p7 | 12:6850878 | AGGTGAACGGGGGTC[C/T]GCCACTCGAGCCAGA | 8078 |
rs782108886 | snp | C/T | | | upstream-variant-2KB, intron-variant | USP5, CDCA3 | GRCh38.p7 | 12:6850269 | GCGATCTGACCACCC[C/T]GGCCTTCCAACGTGC | 8078 |
rs782109862 | snp | C/T | | | intron-variant | USP5 | GRCh38.p7 | 12:6857437 | CTCACCCGGTTTCAT[C/T]TGTCTTCCCTGACCG | 8078 |
rs782110378 | snp | C/T | 4.95397e-05 | 0.00497668 | missense, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6855809 | CGGAAGAAGCCCACG[C/T]GGCTGGCTATTGGTG | 8078 |
rs782110733 | snp | C/G/T | | | intron-variant, downstream-variant-500B | USP5 | GRCh38.p7 | 12:6864411 | ATGCTTCTGTTTGGC[C/G/T]GGGCGCGGTGGCTCA | 8078 |
rs782110827 | snp | C/G | 1.65312e-05 | 0.00287495 | intron-variant | USP5 | GRCh38.p7 | 12:6865160 | CCCCTCTCTCCTTTC[C/G]TAGAGTATCAGCTCT | 8078 |
rs782111097 | snp | C/T | 1.64827e-05 | 0.00287073 | synonymous-codon, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6856830 | CCACGCTGTGGAGCA[C/T]TACCGAGAGACAGGC | 8078 |
rs782111393 | snp | A/G | 7.14094e-05 | 0.00597492 | intron-variant, downstream-variant-500B | USP5 | GRCh38.p7 | 12:6864676 | CCTGGGCGACAGAGC[A/G]AGACTCCGTCTCAAG | 8078 |
rs782117506 | snp | C/G | | | intron-variant | USP5 | GRCh38.p7 | 12:6854347 | TGGGTGCATGTTTAG[C/G]TGTGAGTCCCTAACA | 8078 |
rs782119153 | snp | C/T | 3.303e-05 | 0.00406373 | intron-variant | USP5 | GRCh38.p7 | 12:6856694 | TCTGCTGATTCTCTT[C/T]TCTGTGGGTTAGTGG | 8078 |
rs782120052 | snp | A/G | 1.67083e-05 | 0.00289031 | missense, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6861517 | CCAGAACTGGTTCGG[A/G]CCCAGGTGCCCTTCA | 8078 |
rs782120795 | snp | A/C | 1.64852e-05 | 0.00287094 | synonymous-codon, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6863253 | AGGGCTGCAGCCCGG[A/C]GAGGAGGAGCTGCCA | 8078 |
rs782121425 | snp | A/G | 1.6507e-05 | 0.00287284 | missense, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6855485 | CATTTCAATAAGACC[A/G]GCCAGCGAGTCTACT | 8078 |
rs782124978 | snp | C/T | 8.40103e-05 | 0.00648059 | missense, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6864173 | TCTCCCGGGACCAGG[C/T]CTTGAAAGCGCTGCG | 8078 |
rs782129556 | snp | A/G | | | intron-variant | USP5 | GRCh38.p7 | 12:6862828 | GATAATCTTGAAACA[A/G]TTAATTCTCGTGAGT | 8078 |
rs782131436 | snp | C/G | 1.65375e-05 | 0.0028755 | upstream-variant-2KB, intron-variant | TPI1, USP5 | GRCh38.p7 | 12:6865963 | TTTGTTCATCCTTTT[C/G]TGTTTTCCCCACTTC | 8078 |
rs782132495 | snp | C/T | | | intron-variant | USP5 | GRCh38.p7 | 12:6854081 | AAGGCACTGGAAAAC[C/T]TGGTCAGCTTTGGGG | 8078 |
rs782133247 | snp | G/T | 3.36939e-05 | 0.00410436 | missense, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6861492 | AGCCGAAGAGGAGAA[G/T]ATGGCACTGCCAGAA | 8078 |
rs782136032 | snp | C/T | 1.64887e-05 | 0.00287125 | intron-variant | USP5 | GRCh38.p7 | 12:6860133 | TGAAGTGAAATGTTT[C/T]CTTGGATATTAATGC | 8078 |
rs782137602 | snp | C/T | 2.00572e-05 | 0.00316673 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | USP5, CDCA3 | GRCh38.p7 | 12:6852216 | GCGCTGCTGTCAGTA[C/T]TACCGACGATCCGGG | 8078 |
rs782138836 | in-del | -/C | 1.64811e-05 | 0.00287059 | intron-variant | USP5 | GRCh38.p7 | 12:6856481 | CTGCCTCGGGCACCA[-/C]CCCCCAGAGCAAGGA | 8078 |
rs782139780 | snp | A/G | 3.30087e-05 | 0.00406242 | intron-variant | USP5 | GRCh38.p7 | 12:6859426 | TCCCTTTTCCTCGGC[A/G]CTCAGGCCAGAGCCC | 8078 |
rs782140009 | snp | A/G | 1.648e-05 | 0.0028705 | upstream-variant-2KB, intron-variant | USP5, CDCA3 | GRCh38.p7 | 12:6850602 | AGCTCTCCACCTGTC[A/G]AGACCATAGGCTAGA | 8078 |
rs782140242 | snp | A/T | | | intron-variant | USP5 | GRCh38.p7 | 12:6858843 | GGGCAACATAGCGAG[A/T]CCCTGTCTTCTCTTA | 8078 |
rs782142448 | snp | G/T | 4.94735e-05 | 0.00497336 | missense, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6856717 | GTTAGTGGCTGGAAG[G/T]GCTCCAAGTGTGACA | 8078 |
rs782144258 | snp | G/T | 1.64732e-05 | 0.0028699 | synonymous-codon, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6859518 | TGCCCCGACGGACCC[G/T]ACCCAGGATTTCAGC | 8078 |
rs782145194 | snp | A/C | | | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | USP5, CDCA3 | GRCh38.p7 | 12:6851764 | CCCTCGACTTTCCGA[A/C]CGGACAGGTCCCCAG | 8078 |
rs782147180 | snp | A/G | 1.68752e-05 | 0.00290471 | intron-variant | USP5 | GRCh38.p7 | 12:6858386 | AAAACTACAGGGTTG[A/G]GTTTCTCACTCAGTC | 8078 |
rs782148255 | snp | A/G | 5.09325e-05 | 0.00504615 | upstream-variant-2KB, missense, intron-variant, nc-transcript-variant | USP5, CDCA3 | GRCh38.p7 | 12:6850865 | GGATGCCAGCACTAG[A/G]TGAACGGGGGTCCGC | 8078 |
rs782148625 | snp | A/C/G | 5.06636e-05 | 0.00503286 | missense, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6856429 | TCAAGCAGTTGGACA[A/C/G]CCCTGCTCGAATCCC | 8078 |
rs782149311 | snp | A/T | 1.64735e-05 | 0.00286993 | missense, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6856050 | ACCTTAGCGAGGAGA[A/T]GTTTGAATTAGACGA | 8078 |
rs782151402 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP5, CDCA3 | GRCh38.p7 | 12:6853349 | CCAGTTCAGGATCAT[C/T]ACTGTGATTTGTGGT | 8078 |
rs782151457 | snp | C/T | 3.30087e-05 | 0.00406242 | intron-variant | USP5 | GRCh38.p7 | 12:6857617 | TGATTCTCTTCCTGC[C/T]TCCTGCTCTAGACGT | 8078 |
rs782151989 | snp | G/T | 1.66576e-05 | 0.00288592 | upstream-variant-2KB, intron-variant | TPI1, USP5 | GRCh38.p7 | 12:6865942 | GATGCCACTTTGAAT[G/T]CCCAGTTTGTTCATC | 8078 |
rs782154447 | snp | A/G | 3.32651e-05 | 0.00407817 | synonymous-codon | USP5 | GRCh38.p7 | 12:6864745 | TTTAGAACGGGCTGT[A/G]GACTGGATCTTCAGT | 8078 |
rs782154838 | snp | C/T | 1.65356e-05 | 0.00287533 | synonymous-codon | USP5 | GRCh38.p7 | 12:6864778 | CATTGACGACCTGGA[C/T]GCTGAAGCTGCCATG | 8078 |
rs782158801 | snp | A/G | | | intron-variant | USP5 | GRCh38.p7 | 12:6862983 | CATAGATTATTTATG[A/G]TAGATCTAGGACCAG | 8078 |
rs782161191 | snp | C/T | 0.000149352 | 0.00864022 | intron-variant | USP5 | GRCh38.p7 | 12:6856680 | CCCCGACCCACATTT[C/T]TGCTGATTCTCTTCT | 8078 |
rs782162941 | snp | A/G | 1.84578e-05 | 0.00303786 | intron-variant | USP5 | GRCh38.p7 | 12:6861633 | GTAAGTCCTCTGGTC[A/G]GGGCCTGAGGCTGTG | 8078 |
rs782164008 | snp | C/G | 3.29696e-05 | 0.00406001 | synonymous-codon, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6862548 | CTTAGACTGGGTGCC[C/G]AAGAAACTGGGTATG | 8078 |
rs782164152 | snp | A/T | 6.87545e-05 | 0.00586281 | intron-variant | USP5 | GRCh38.p7 | 12:6864042 | CATCAACCCCTTCAC[A/T]TCCACAGATTTTGCA | 8078 |
rs782164807 | snp | A/C | | | upstream-variant-2KB, intron-variant | TPI1, USP5 | GRCh38.p7 | 12:6867040 | CCTGCATTTGTCCCG[A/C]AAGTTTTCACTCAGG | 8078 |
rs782164999 | in-del | -/C | 1.65218e-05 | 0.00287413 | intron-variant | USP5 | GRCh38.p7 | 12:6857730 | ATGCAGAAGGTGAGA[-/C]CCCCTTCAACTTCAG | 8078 |
rs782165647 | snp | G/T | 1.82184e-05 | 0.00301809 | intron-variant | USP5 | GRCh38.p7 | 12:6861393 | GGAGAGGCTAAGGAG[G/T]CAAAGAAGCAGCACC | 8078 |
rs782167420 | snp | A/G | 6.58903e-05 | 0.00573941 | synonymous-codon, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6861009 | CTTCTTGGTGGAGGA[A/G]AAGATCAAGTGCCTG | 8078 |
rs782169796 | snp | C/T | 0.000362552 | 0.013459 | synonymous-codon, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6856027 | TCCAGGTGTTGAAGG[C/T]GGATTTGACCTTAGC | 8078 |
rs782170638 | snp | A/G | 3.29484e-05 | 0.00405871 | missense, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6859477 | ACTTTTAGGTATGTG[A/G]ATAAGCTGGAGAAGA | 8078 |
rs782170720 | snp | A/G | | | intron-variant | USP5 | GRCh38.p7 | 12:6859281 | CCGCCGAGCGTGCTT[A/G]CACATTGGACATAGC | 8078 |
rs782170955 | snp | C/G | | | intron-variant | USP5 | GRCh38.p7 | 12:6857073 | GGAGAATTGCTTGAG[C/G]CTAGGAGTTCGAGAC | 8078 |
rs782173242 | snp | C/G | | | upstream-variant-2KB, intron-variant | TPI1, USP5 | GRCh38.p7 | 12:6865663 | CAGGAAAGTTGAGTC[C/G]TTGTGTCAGAGACCA | 8078 |
rs782174824 | snp | A/G | | | intron-variant | USP5 | GRCh38.p7 | 12:6858005 | TTCCCAGATAAATAA[A/G]TGAATAGTTGCAAAC | 8078 |
rs782177096 | snp | A/C/G | 3.46899e-05 | 0.00416461 | intron-variant | USP5 | GRCh38.p7 | 12:6864021 | GCCTCCATCCTCCCC[A/C/G]AAACACATCAACCCC | 8078 |
rs782177488 | snp | C/T | 1.80029e-05 | 0.00300019 | intron-variant | USP5 | GRCh38.p7 | 12:6856903 | GCTGGTACAGCCTCC[C/T]CTCCTCCAGCCACTC | 8078 |
rs782178379 | snp | A/T | | | intron-variant | USP5 | GRCh38.p7 | 12:6858402 | GTTTCTCACTCAGTC[A/T]GAAGTGCCCCTTCTC | 8078 |
rs782181102 | snp | C/T | 1.64991e-05 | 0.00287215 | intron-variant | USP5 | GRCh38.p7 | 12:6856010 | CTCTTCTTCCCTATC[C/T]TTCCAGGTGTTGAAG | 8078 |
rs782182078 | snp | A/G | 1.66824e-05 | 0.00288806 | upstream-variant-2KB, utr-variant-3-prime | TPI1, USP5 | GRCh38.p7 | 12:6866111 | ACCAATGAGGGCAGG[A/G]GAAGACCACCTGGCA | 8078 |
rs782182525 | snp | A/G | 1.65351e-05 | 0.00287528 | intron-variant | USP5 | GRCh38.p7 | 12:6856198 | AGAGCAAGATGGGCC[A/G]GGGTAGTGGTGTCTT | 8078 |
rs782182837 | snp | A/G | | | intron-variant | USP5 | GRCh38.p7 | 12:6863111 | AGTTCTGACATAGGG[A/G]GCAGGGGATTGAGGT | 8078 |
rs782183452 | snp | A/G | | | intron-variant | USP5 | GRCh38.p7 | 12:6860645 | CACCTGAGGAGGACA[A/G]TGAAGGTGATGATCC | 8078 |
rs782184177 | snp | A/G | 1.68303e-05 | 0.00290084 | missense, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6863883 | GAGATGGGATTCCCT[A/G]TGGACGCCTGCCGCA | 8078 |
rs782184595 | snp | C/G/T | | | intron-variant | USP5 | GRCh38.p7 | 12:6862083 | TCCTCTCTGTGTGGG[C/G/T]TTTTTTTTTTTTTCT | 8078 |
rs782184869 | snp | A/G | 4.95291e-05 | 0.00497615 | intron-variant | USP5 | GRCh38.p7 | 12:6856166 | GTATGACTGCCCCCT[A/G]TGCTACCCAAGATTC | 8078 |
rs782186396 | snp | G/T | | | upstream-variant-2KB, intron-variant | USP5, CDCA3 | GRCh38.p7 | 12:6851060 | TTCCACGTCGGACCT[G/T]CAACCCTAAACCACC | 8078 |
rs782187171 | snp | C/T | 1.73243e-05 | 0.0029431 | intron-variant, downstream-variant-500B | USP5 | GRCh38.p7 | 12:6864207 | CACGGTATGGGCTGC[C/T]CCAGCTAAGGACATG | 8078 |
rs782187698 | in-del | -/G | 1.65315e-05 | 0.00287498 | intron-variant | USP5 | GRCh38.p7 | 12:6855982 | TGACCTGTTGTCATT[-/G]GCTCTACTCTCCCTC | 8078 |
rs782187846 | snp | A/T | | | intron-variant, upstream-variant-2KB | USP5, CDCA3 | GRCh38.p7 | 12:6853686 | TTTTGTAATCTTCTG[A/T]AACTTTCCCTTTTTC | 8078 |
rs782187979 | snp | C/T | 3.31148e-05 | 0.00406894 | intron-variant | USP5 | GRCh38.p7 | 12:6855726 | CGCTCGTGCTCATTG[C/T]TGATCCAGCCCTTCC | 8078 |
rs782188663 | snp | C/T | | | upstream-variant-2KB, intron-variant | USP5, CDCA3 | GRCh38.p7 | 12:6850649 | ACTCTTCTCTCCTCT[C/T]CTCCCCATATTCCAG | 8078 |
rs782190611 | snp | A/G | 2.75213e-05 | 0.00370943 | intron-variant, upstream-variant-2KB | USP5, CDCA3 | GRCh38.p7 | 12:6852299 | CACGCCGGTAAGCCC[A/G]TTCCCCACGCCCGCA | 8078 |
rs782191384 | snp | C/T | 3.32187e-05 | 0.00407532 | missense | USP5 | GRCh38.p7 | 12:6865224 | TGTGTGGTCACTACG[C/T]CTGCCACATCAAGAA | 8078 |
rs782192969 | snp | C/G | 1.6582e-05 | 0.00287936 | missense | USP5 | GRCh38.p7 | 12:6864869 | AAAGTCCGGGATGGT[C/G]CTGGAAGTGAGTATC | 8078 |
rs782195671 | snp | C/T | 1.64757e-05 | 0.00287012 | intron-variant | USP5 | GRCh38.p7 | 12:6862461 | ACCAGCACAGTCTCT[C/T]TTCCCTAGGACCACA | 8078 |
rs782195950 | snp | A/T | 1.65239e-05 | 0.00287431 | intron-variant | USP5 | GRCh38.p7 | 12:6860932 | CTGCCCAGACCTCCC[A/T]ACCCTGCCTCTTTCC | 8078 |
rs782197438 | snp | A/C | | | upstream-variant-2KB, intron-variant | USP5, CDCA3 | GRCh38.p7 | 12:6850391 | CTTTAAGGAACCCTG[A/C]GAGAATGGCTTCATG | 8078 |
rs782197476 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP5, CDCA3 | GRCh38.p7 | 12:6852629 | AAACCTGGCAGTCGG[C/T]CTTGTCTGCCGCGCA | 8078 |
rs782197717 | snp | C/G | 1.6476e-05 | 0.00287014 | missense, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6856802 | GCTACTTCGATGGCA[C/G]TGGGGGCAACAACCA | 8078 |
rs782198305 | snp | G/T | | | upstream-variant-2KB, utr-variant-3-prime | TPI1, USP5 | GRCh38.p7 | 12:6866510 | GGTCAAGGAGGGATG[G/T]GAGGGAAATAGGGAC | 8078 |
rs782199741 | snp | A/C | 1.64836e-05 | 0.0028708 | missense, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6858511 | TCAGGTGTGCCACTC[A/C]AGCCCCTGTTTGGGC | 8078 |
rs782203515 | snp | C/G | | | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | USP5, CDCA3 | GRCh38.p7 | 12:6851459 | TTGCCCAGGGGTGAC[C/G]CCTCCTTGATAAGGG | 8078 |
rs782203923 | snp | G/T | 1.64765e-05 | 0.00287019 | missense, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6856125 | GGGATGGACTGGGGG[G/T]ACTGCCTGACATTGT | 8078 |
rs782203984 | snp | A/G | 0.000395778 | 0.0140617 | missense, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6855476 | GTGGAGAGACATTTC[A/G]ATAAGACCGGCCAGC | 8078 |
rs782204466 | snp | G/T | | | intron-variant | USP5 | GRCh38.p7 | 12:6863412 | GCCTGTCTCTCTCCC[G/T]TGCTGATGGGGGCCT | 8078 |
rs782205180 | snp | A/G | | | intron-variant, downstream-variant-500B | USP5 | GRCh38.p7 | 12:6864569 | TGGTGGGCGTCTGTA[A/G]TCCCAGCTACTTGGG | 8078 |
rs782205703 | snp | C/G | 1.6486e-05 | 0.00287102 | missense, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6860189 | TCTCCGGGGAGTATT[C/G]CAAGCCAGTACCGGA | 8078 |
rs782208885 | snp | C/G | 2.35136e-05 | 0.00342874 | intron-variant | USP5 | GRCh38.p7 | 12:6858666 | CCTGGTCAGCACCCT[C/G]TGGGCATACTCCTCC | 8078 |
rs782208963 | snp | G/T | | | intron-variant | USP5 | GRCh38.p7 | 12:6859303 | GGACATAGCTGAGAA[G/T]GGGAGAACAGGCAGG | 8078 |
rs782210069 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | USP5, CDCA3 | GRCh38.p7 | 12:6851382 | CTCGAGCCAAAGGAA[A/G]CTGTTGGTCTGGGAG | 8078 |
rs782210466 | snp | A/G | 1.79345e-05 | 0.00299448 | upstream-variant-2KB, missense, intron-variant, nc-transcript-variant | USP5, CDCA3 | GRCh38.p7 | 12:6850931 | GCGCTGGTGTGACTG[A/G]GACGCTCTTGGCTGA | 8078 |
rs782210685 | snp | C/T | 3.36836e-05 | 0.00410374 | intron-variant | USP5 | GRCh38.p7 | 12:6856290 | GTATTGCCTCTGACC[C/T]TCTGCTTCCCCCAGG | 8078 |
rs782212714 | snp | C/T | 1.64819e-05 | 0.00287066 | upstream-variant-2KB, intron-variant | USP5, CDCA3 | GRCh38.p7 | 12:6850448 | AGCTTCATCAGCATT[C/T]CCTGGGCCCAACGCT | 8078 |
rs782213243 | snp | A/C | 6.34035e-05 | 0.00563007 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | USP5, CDCA3 | GRCh38.p7 | 12:6852152 | AACGGTGGGAGCCGC[A/C]GTGTGTGGAGAAGCT | 8078 |
rs782217204 | snp | C/T | | | intron-variant, downstream-variant-500B | USP5 | GRCh38.p7 | 12:6864516 | AACACGGTGAAACCC[C/T]GTCTCTACGAAAAAT | 8078 |
rs782218014 | snp | A/G | 1.66421e-05 | 0.00288458 | intron-variant | USP5 | GRCh38.p7 | 12:6855533 | CGGCGCCCGGTAGGA[A/G]CAGGGCTGGGGCAAG | 8078 |
rs782219129 | snp | C/G | | | intron-variant | USP5 | GRCh38.p7 | 12:6855690 | CTACCTCCTTCCGTC[C/G]CTCCTCCCGACTTGT | 8078 |
rs782221266 | snp | C/T | 1.68131e-05 | 0.00289935 | intron-variant | USP5 | GRCh38.p7 | 12:6865134 | ATTCCTCTTCTGTTT[C/T]CTTCTCTGACCCCCT | 8078 |
rs782222479 | snp | C/T | | | intron-variant, downstream-variant-500B | USP5 | GRCh38.p7 | 12:6864572 | TGGGCGTCTGTAGTC[C/T]CAGCTACTTGGGAGG | 8078 |
rs782222761 | snp | A/C | 4.96381e-05 | 0.00498162 | missense, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6864116 | GCGCAGCAGCCGACC[A/C]CCCTCCTGAGGACTG | 8078 |
rs782224740 | snp | A/G | | | upstream-variant-2KB, intron-variant | TPI1, USP5 | GRCh38.p7 | 12:6865827 | GACCCTTGTGAGGTT[A/G]TGAAGCTCCCTTAAG | 8078 |
rs782225812 | snp | A/C | 1.79024e-05 | 0.0029918 | intron-variant, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6863158 | AGGTAGGCCTCCGGG[A/C]GCTGCTGAGGTGACC | 8078 |
rs782226684 | snp | A/G | | | intron-variant | USP5 | GRCh38.p7 | 12:6859972 | CACTGGCCTATTAGG[A/G]GCATTCGGGTGACTG | 8078 |
rs782228350 | snp | A/G | 1.65168e-05 | 0.00287369 | intron-variant | USP5 | GRCh38.p7 | 12:6860271 | TCCCTTTCAGGCCCT[A/G]GGATTGTGGGGAAGC | 8078 |
rs782228614 | snp | C/T | | | intron-variant | USP5 | GRCh38.p7 | 12:6857486 | TGACCGCACTCATAT[C/T]ACTCATATTCAAGGG | 8078 |
rs782230741 | snp | C/G | | | intron-variant | USP5 | GRCh38.p7 | 12:6854399 | CACACTTCAGCAGGA[C/G]AGGAGGGAGAAGACT | 8078 |
rs782232671 | snp | A/G | 1.73933e-05 | 0.00294895 | missense, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6861470 | AGTACGAGGAGAAGA[A/G]GCGGCAAGCCGAAGA | 8078 |
rs782233822 | in-del | -/CCTG | 3.38825e-05 | 0.00411584 | intron-variant | USP5 | GRCh38.p7 | 12:6863393 | TTAGTGACTCTTCTT[-/CCTG]CCTGCCTGTCTCTCT | 8078 |
rs782234077 | snp | C/T | 1.64882e-05 | 0.00287121 | intron-variant | USP5 | GRCh38.p7 | 12:6860950 | CCTGCCTCTTTCCCA[C/T]AGAGGAATTGCCGGA | 8078 |
rs782235822 | snp | G/T | 6.24746e-05 | 0.00558869 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | USP5, CDCA3 | GRCh38.p7 | 12:6852154 | CGGTGGGAGCCGCCG[G/T]GTGTGGAGAAGCTGC | 8078 |
rs782238819 | snp | A/G | 3.29815e-05 | 0.00406075 | synonymous-codon, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6860202 | TTCCAAGCCAGTACC[A/G]GAGTCGGGCGATGGG | 8078 |
rs782239317 | snp | A/G | 1.65594e-05 | 0.0028774 | intron-variant | USP5 | GRCh38.p7 | 12:6855716 | CTTGTTCCTTCGCTC[A/G]TGCTCATTGCTGATC | 8078 |
rs782240204 | in-del | -/G | 3.0427e-05 | 0.00390033 | intron-variant, upstream-variant-2KB | USP5, CDCA3 | GRCh38.p7 | 12:6852308 | AAGCCCATTCCCCAC[-/G]CCCGCAACGAGCACG | 8078 |
rs782241158 | snp | C/T | 1.73093e-05 | 0.00294183 | missense, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6861587 | ATGACTTCTGGAGCA[C/T]GGCCCTGCAGGCCAA | 8078 |
rs782242694 | snp | A/G | | | missense, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6861467 | TGGAGTACGAGGAGA[A/G]GAAGCGGCAAGCCGA | 8078 |
rs782243097 | snp | A/G | 1.67978e-05 | 0.00289804 | upstream-variant-2KB, synonymous-codon, intron-variant, nc-transcript-variant | USP5, CDCA3 | GRCh38.p7 | 12:6850836 | GGCCCAGAGTACCTG[A/G]ATGGGAGTGCGCAGG | 8078 |
rs782243746 | snp | C/T | 2.33011e-05 | 0.00341321 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | USP5, CDCA3 | GRCh38.p7 | 12:6852278 | CGAGTGCGCCTTCTC[C/T]TTCGACACGCCGGTA | 8078 |
rs782243971 | snp | C/T | 1.65419e-05 | 0.00287588 | missense, intron-variant, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6863348 | AAGACGAAGACTCCT[C/T]CTGCTCCCCTCACTT | 8078 |
rs782244235 | snp | C/T | 6.59185e-05 | 0.00574064 | synonymous-codon, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6855440 | TGTATGAACACGTTT[C/T]TGGGCTTTGGGAAAC | 8078 |
rs782248865 | snp | A/G | 1.96254e-05 | 0.00313246 | upstream-variant-2KB, utr-variant-5-prime, intron-variant, nc-transcript-variant | USP5, CDCA3 | GRCh38.p7 | 12:6850987 | GTGGGGGCAAGGGCC[A/G]GCCCGGGACGAGGAG | 8078 |
rs782249151 | snp | C/G | | | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | USP5, CDCA3 | GRCh38.p7 | 12:6852038 | CGGAGCACCGGCAGG[C/G]AGGCTCCGTCCAACT | 8078 |
rs782249338 | snp | C/G | 1.65679e-05 | 0.00287814 | missense, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6860458 | GCAGCAGGATGCCCA[C/G]GAGTTCTTCCTTCAC | 8078 |
rs782249366 | snp | C/T | | | intron-variant | USP5 | GRCh38.p7 | 12:6865348 | GAGAAGGTGAAGGGA[C/T]TGCCTGATGGGGACA | 8078 |
rs782250627 | snp | A/G | 3.29468e-05 | 0.00405861 | missense, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6856110 | ACCTGGAGATTGCCC[A/G]GGATGGACTGGGGGG | 8078 |
rs782253527 | snp | G/T | | | intron-variant | USP5 | GRCh38.p7 | 12:6863544 | TCCTAGCCACCTTCT[G/T]GGTGTGGATGGCAGC | 8078 |
rs782254816 | snp | C/G | 1.65318e-05 | 0.002875 | synonymous-codon | USP5 | GRCh38.p7 | 12:6864847 | TGAGTCTGTGCCAGT[C/G]GGACCTAAAGTCCGG | 8078 |
rs782256062 | snp | A/G | 1.75348e-05 | 0.00296093 | synonymous-codon, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6861462 | GCTTCTGGAGTACGA[A/G]GAGAAGAAGCGGCAA | 8078 |
rs782259794 | snp | C/G/T | 0.000100396 | 0.00708448 | intron-variant | USP5 | GRCh38.p7 | 12:6856668 | ACTCCCTCAAATCCC[C/G/T]GACCCACATTTCTGC | 8078 |
rs782260290 | snp | A/G | | | intron-variant | USP5 | GRCh38.p7 | 12:6857014 | AAAGTAGTCAGGTGC[A/G]GTGGCTCATGTTTGC | 8078 |
rs782260845 | snp | G/T | 8.2373e-05 | 0.00641714 | missense, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6862486 | ACCACACGATTTGCC[G/T]CATTCCCTGACTACC | 8078 |
rs782262195 | snp | C/T | | | intron-variant | USP5 | GRCh38.p7 | 12:6857199 | CTCAGGAGGCTGAGG[C/T]AGGAGGATTGTTTGA | 8078 |
rs782262313 | snp | C/T | | | upstream-variant-2KB, utr-variant-3-prime | TPI1, USP5 | GRCh38.p7 | 12:6866366 | TCTGCTTCTCTGTGT[C/T]GCCCCGCCCAGCCCC | 8078 |
rs782262896 | snp | A/G | | | intron-variant | USP5 | GRCh38.p7 | 12:6859979 | CTATTAGGAGCATTC[A/G]GGTGACTGTCTTCTG | 8078 |
rs782263391 | snp | G/T | 1.73522e-05 | 0.00294547 | intron-variant | USP5 | GRCh38.p7 | 12:6864006 | GCAGGGTGGGGCAGG[G/T]CCTCCATCCTCCCCC | 8078 |
rs782264039 | snp | C/T | 3.30644e-05 | 0.00406585 | intron-variant | USP5 | GRCh38.p7 | 12:6855981 | ATTGACCTGTTGTCA[C/T]TGCTCTACTCTCCCT | 8078 |
rs782267655 | snp | C/T | | | intron-variant | USP5 | GRCh38.p7 | 12:6861258 | TAGGTAGATTAACCT[C/T]GTCCAGTGGACACTC | 8078 |
rs782267716 | snp | A/C/G | 6.61819e-05 | 0.00575216 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | USP5, CDCA3 | GRCh38.p7 | 12:6852148 | TGGGAACGGTGGGAG[A/C/G]CGCCGTGTGTGGAGA | 8078 |
rs782270888 | snp | C/T | 1.64765e-05 | 0.00287019 | upstream-variant-2KB, synonymous-codon, utr-variant-5-prime, nc-transcript-variant | USP5, CDCA3 | GRCh38.p7 | 12:6850567 | CAGTTGCTCCCCTGC[C/T]GGTAGGCCTGGCTGT | 8078 |
rs782273234 | snp | C/T | 1.64841e-05 | 0.00287085 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | USP5, CDCA3 | GRCh38.p7 | 12:6852169 | TGTGTGGAGAAGCTG[C/T]TGCCGGTGTCATGGC | 8078 |
rs782277301 | snp | C/T | 2.05573e-05 | 0.00320597 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | USP5, CDCA3 | GRCh38.p7 | 12:6852207 | AGTGAGGAGGCGCTG[C/T]TGTCAGTATTACCGA | 8078 |
rs782277992 | snp | A/G | | | intron-variant | USP5 | GRCh38.p7 | 12:6854713 | CAGTGAGCTATGATC[A/G]TGCCACTGCACTCCA | 8078 |
rs782281874 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | USP5, CDCA3 | GRCh38.p7 | 12:6851499 | TCAGTATCGGCCTGC[A/G]AGCCGTCCGTGGCAG | 8078 |
rs782281944 | snp | A/G | 1.68863e-05 | 0.00290566 | upstream-variant-2KB, intron-variant | USP5, CDCA3 | GRCh38.p7 | 12:6850818 | CTCTGCCTTTCCCAC[A/G]CTGGCCCAGAGTACC | 8078 |
rs782287315 | snp | C/T | 1.69258e-05 | 0.00290905 | synonymous-codon, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6863196 | CACAGATGTGTCCAT[C/T]GAGATGCCAGAGGAG | 8078 |
rs782287975 | snp | C/G | 1.64923e-05 | 0.00287156 | missense, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6855409 | CCCACAGGAGTCTGA[C/G]GGGGGCCTCTACATC | 8078 |
rs782288684 | snp | A/G | 1.65143e-05 | 0.00287348 | intron-variant | USP5 | GRCh38.p7 | 12:6860285 | TGGGATTGTGGGGAA[A/G]CTGAGGTCTGGGAGA | 8078 |
rs782289463 | in-del | -/TTTTG | | | intron-variant | USP5 | GRCh38.p7 | 12:6859650 | CCTGGCCTTTTTTTG[-/TTTTG]TTTTGTTTTGTTTTG | 8078 |
rs782291039 | snp | A/G | 1.6473e-05 | 0.00286988 | synonymous-codon, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6859491 | GGATAAGCTGGAGAA[A/G]ATCTTCCAGAATGCC | 8078 |
rs782292044 | in-del | -/GG | | | intron-variant | USP5 | GRCh38.p7 | 12:6863703 | TTGGTTTTGGGATAA[-/GG]GGTGCCAATCCATGG | 8078 |
rs782293734 | snp | G/T | 0.029809 | 0.118389 | missense, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6856393 | GGGAAGTACGGCAGG[G/T]GTCTAAGCATGCCTT | 8078 |
rs782295839 | snp | C/G | 1.74287e-05 | 0.00295196 | intron-variant | USP5 | GRCh38.p7 | 12:6856918 | CCTCCTCCAGCCACT[C/G]TCATGCTTAAATATA | 8078 |
rs782295979 | snp | A/G | 1.89669e-05 | 0.00307946 | upstream-variant-2KB, utr-variant-5-prime, intron-variant, nc-transcript-variant | USP5, CDCA3 | GRCh38.p7 | 12:6850971 | AACCAGGAGTTGCAG[A/G]GTGGGGGCAAGGGCC | 8078 |
rs782296988 | snp | C/T | | | intron-variant | USP5 | GRCh38.p7 | 12:6854875 | GAAGGTTTTCTGAAT[C/T]ATGGAGATGAGATAG | 8078 |
rs782298280 | snp | A/G | 1.68766e-05 | 0.00290483 | intron-variant | USP5 | GRCh38.p7 | 12:6856262 | AAGAGGGGCATGTGG[A/G]GCAGGGGGTTGGGTA | 8078 |
rs782298906 | snp | C/T | | | intron-variant | USP5 | GRCh38.p7 | 12:6863456 | CCCCTGCCCCTGTCC[C/T]TTGTGTTTCTCCTGT | 8078 |
rs782299787 | snp | C/G | 0.000243082 | 0.0110219 | intron-variant | USP5 | GRCh38.p7 | 12:6858647 | CTCCTTCCCCAGGCC[C/G]CCTCCTGGTCAGCAC | 8078 |
rs782302639 | in-del | -/T | | | intron-variant | USP5 | GRCh38.p7 | 12:6855996 | TTGCTCTACTCTCCC[-/T]CTTCTTCCCTATCCT | 8078 |
rs782302925 | snp | A/G | 1.65419e-05 | 0.00287588 | intron-variant | USP5 | GRCh38.p7 | 12:6855743 | GATCCAGCCCTTCCT[A/G]CTTCTTTACAGAAAG | 8078 |
rs782305009 | snp | C/G | 1.66029e-05 | 0.00288117 | missense, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6860479 | CTTCCTTCACCTTAT[C/G]AACATGGTGGAGGTA | 8078 |
rs782305326 | snp | C/T | 1.65143e-05 | 0.00287348 | intron-variant, upstream-variant-2KB | USP5, CDCA3 | GRCh38.p7 | 12:6852303 | CCGGTAAGCCCATTC[C/T]CCACGCCCGCAACGA | 8078 |
rs782306188 | snp | C/G | | | intron-variant, upstream-variant-2KB | USP5, CDCA3 | GRCh38.p7 | 12:6852418 | TTGTAGTCTCCCACG[C/G]TCCACTCTGCCGTTG | 8078 |
rs782307575 | snp | A/G | | | intron-variant | USP5 | GRCh38.p7 | 12:6855046 | GATCTGTTAGCCCCA[A/G]GATAGAGGTGAAGGA | 8078 |
rs782308916 | snp | A/C | 3.36462e-05 | 0.00410146 | upstream-variant-2KB, missense, intron-variant, nc-transcript-variant | USP5, CDCA3 | GRCh38.p7 | 12:6850846 | ACCTGGATGGGAGTG[A/C]GCAGGATGCCAGCAC | 8078 |
rs782310030 | snp | C/G | | | intron-variant | USP5 | GRCh38.p7 | 12:6857148 | AAAAAAGAAAAATTG[C/G]CTGGGTGTGGTAGCT | 8078 |
rs782310192 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP5, CDCA3 | GRCh38.p7 | 12:6853950 | GAGAAATGTTCAAGG[C/T]CACTGAGACTTTTAT | 8078 |
rs782310395 | snp | A/G | | | intron-variant | USP5 | GRCh38.p7 | 12:6865346 | GGGAGAAGGTGAAGG[A/G]ACTGCCTGATGGGGA | 8078 |
rs782311944 | snp | C/T | 1.64732e-05 | 0.0028699 | missense, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6859511 | TCCAGAATGCCCCGA[C/T]GGACCCTACCCAGGA | 8078 |
rs782315188 | snp | C/T | 1.65146e-05 | 0.0028735 | intron-variant | USP5 | GRCh38.p7 | 12:6860275 | TTTCAGGCCCTGGGA[C/T]TGTGGGGAAGCTGAG | 8078 |
rs782315838 | snp | A/C | 1.65274e-05 | 0.00287462 | intron-variant | USP5 | GRCh38.p7 | 12:6857738 | GGTGAGACCCCCTTC[A/C]ACTTCAGATTCTTCT | 8078 |
rs782316457 | snp | A/G | 0.000122093 | 0.00781226 | upstream-variant-2KB, utr-variant-5-prime, intron-variant, nc-transcript-variant | USP5, CDCA3 | GRCh38.p7 | 12:6850992 | GGCAAGGGCCAGCCC[A/G]GGACGAGGAGGGAAT | 8078 |
rs782317464 | snp | A/G | 1.65886e-05 | 0.00287993 | intron-variant | USP5 | GRCh38.p7 | 12:6857767 | CTACTTCCTGCCCCT[A/G]TGAGGGCCCTTCCTC | 8078 |
rs782318022 | snp | A/T | 1.6483e-05 | 0.00287076 | missense, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6856023 | TCCTTCCAGGTGTTG[A/T]AGGCGGATTTGACCT | 8078 |
rs782318890 | snp | C/T | 6.67423e-05 | 0.00577639 | missense | USP5 | GRCh38.p7 | 12:6864737 | AACAATAGTTTAGAA[C/T]GGGCTGTGGACTGGA | 8078 |
rs782322104 | snp | C/G | 1.7342e-05 | 0.0029446 | intron-variant, downstream-variant-500B | USP5 | GRCh38.p7 | 12:6864208 | ACGGTATGGGCTGCC[C/G]CAGCTAAGGACATGG | 8078 |
rs782324656 | snp | C/G | 1.65559e-05 | 0.00287709 | missense, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6856387 | GGGATGGGGAAGTAC[C/G]GCAGGTGTCTAAGCA | 8078 |
rs782325356 | snp | A/G | | | intron-variant | USP5 | GRCh38.p7 | 12:6863525 | TGGGGCCTCCCCAGC[A/G]CACTCCTAGCCACCT | 8078 |
rs782329393 | snp | A/C | | | intron-variant | USP5 | GRCh38.p7 | 12:6857853 | AAGATACACAGGCTT[A/C]TTTTAAATATCTAAA | 8078 |
rs782330344 | snp | A/C | 1.65097e-05 | 0.00287308 | synonymous-codon, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6863235 | CTCCCAGTTGAGGGG[A/C]ACAGGGCTGCAGCCC | 8078 |
rs782331280 | in-del | -/A | | | intron-variant | USP5 | GRCh38.p7 | 12:6862626 | GGCTTTAACACATAT[-/A]AACTAGTGTTTCTCA | 8078 |
rs782331322 | snp | A/T | | | intron-variant | USP5 | GRCh38.p7 | 12:6862358 | GAAGAATATGGAGGA[A/T]CTTCTGGGTTATTGG | 8078 |
rs782332700 | snp | A/G | 1.65026e-05 | 0.00287246 | missense | USP5 | GRCh38.p7 | 12:6865248 | TCAAGAAAGAAGGCA[A/G]GTGAGTGCTGGCCAC | 8078 |
rs782333337 | snp | C/T | 1.68391e-05 | 0.0029016 | missense, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6863884 | AGATGGGATTCCCTA[C/T]GGACGCCTGCCGCAA | 8078 |
rs782333998 | snp | A/G | 1.6473e-05 | 0.00286988 | missense, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6861001 | GTGTTCCGCTTCTTG[A/G]TGGAGGAAAAGATCA | 8078 |
rs782334370 | snp | A/G | 2.30285e-05 | 0.00339319 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | USP5, CDCA3 | GRCh38.p7 | 12:6852188 | CGGTGTCATGGCGGA[A/G]CTGAGTGAGGAGGCG | 8078 |
rs782336145 | snp | A/G | | | intron-variant | USP5 | GRCh38.p7 | 12:6859342 | GAGAAGCGACTCCAA[A/G]GTTCACCCACAGCAA | 8078 |
rs782336796 | snp | A/C | 1.73863e-05 | 0.00294836 | intron-variant | USP5 | GRCh38.p7 | 12:6864007 | CAGGGTGGGGCAGGG[A/C]CTCCATCCTCCCCCA | 8078 |
rs782336827 | snp | A/G | 3.32856e-05 | 0.00407942 | intron-variant | USP5 | GRCh38.p7 | 12:6855535 | GCGCCCGGTAGGAGC[A/G]GGGCTGGGGCAAGGC | 8078 |
rs782338190 | snp | A/G | | | intron-variant | USP5 | GRCh38.p7 | 12:6854104 | CTTTGGGGGAAGCCC[A/G]TCCTCCCTTCTCAGC | 8078 |
rs782338288 | snp | G/T | | | intron-variant | USP5 | GRCh38.p7 | 12:6860834 | GTTTCTGCTCTGCTC[G/T]TGTGTCCCTGAGTTC | 8078 |
rs782338672 | snp | A/C | 1.6477e-05 | 0.00287024 | synonymous-codon, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6862509 | TGACTACCTGGTCAT[A/C]CAGATCAAGAAGTTC | 8078 |
rs782343189 | snp | A/G | 1.65433e-05 | 0.002876 | intron-variant | USP5 | GRCh38.p7 | 12:6861145 | CGTGGCACGGTGGGA[A/G]GCTAAGGTCTAGGAG | 8078 |
rs782343776 | snp | A/G | 1.65318e-05 | 0.002875 | intron-variant | USP5 | GRCh38.p7 | 12:6855988 | TGTTGTCATTGCTCT[A/G]CTCTCCCTCTTCTTC | 8078 |
rs782344516 | snp | C/T | 1.65211e-05 | 0.00287407 | missense, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6855771 | AAGAGGAGGACCCTG[C/T]TACAGGCACTGGAGA | 8078 |
rs782344804 | snp | A/G | | | intron-variant | USP5 | GRCh38.p7 | 12:6857804 | TGAGGCTGAGGTAGG[A/G]TTTTGGAGAAATCTT | 8078 |
rs782345305 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP5, CDCA3 | GRCh38.p7 | 12:6853343 | TGAGGCCCAGTTCAG[A/G]ATCATCACTGTGATT | 8078 |
rs782347361 | snp | C/G | 1.71596e-05 | 0.00292908 | missense, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6863859 | GAATCAGTCATCATC[C/G]AGCTGGTGGAGATGG | 8078 |
rs782347821 | snp | C/T | | | upstream-variant-2KB, intron-variant | USP5, CDCA3 | GRCh38.p7 | 12:6851126 | CGAGGGACCAGAGGC[C/T]TCTGCGGAGTTAATG | 8078 |
rs782350513 | in-del | -/C | 0.000100759 | 0.00709714 | intron-variant, upstream-variant-2KB | USP5, CDCA3 | GRCh38.p7 | 12:6852315 | TCCCCACGCCCGCAA[-/C]CGAGCACGACTTCCT | 8078 |
rs782355182 | snp | A/G | | | intron-variant | USP5 | GRCh38.p7 | 12:6861851 | TCTTCTGTGGCACAG[A/G]GTCTCTTTGTAGTGT | 8078 |