SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs971281 | snp | A/G | 0.391583 | 0.206044 | intron-variant | USP16 | GRCh38.p7 | 21:29047958 | TATGTATATATATAT[A/G]TGTGTGTGTATGTAT | 10600 |
rs1034123 | snp | A/G | 0.222928 | 0.24853 | intron-variant, upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29026978 | CTGTTAAATGCTTCC[A/G]ATCAAGAGAGTGATA | 10600 |
rs2210256 | snp | A/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29040581 | ttaaaatttaatagt[A/T]tatatatatCCATTT | 10600 |
rs2225420 | snp | A/G | 0 | 0 | intron-variant | USP16 | GRCh38.p7 | 21:29040819 | TCAACGTTGATTAGT[A/G]AAAATTATTCAGTGC | 10600 |
rs2245962 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | USP16 | GRCh38.p7 | 21:29049472 | AAAGTATTATGCTAT[C/T]GCTGAGTTTTAAGCA | 10600 |
rs2254872 | snp | C/T | 0.415563 | 0.18732 | intron-variant | USP16 | GRCh38.p7 | 21:29042403 | CCCCATCCCACAGGG[C/T]AGGGAGGATCTTACT | 10600 |
rs2274802 | snp | A/T | 0.334703 | 0.235213 | missense, utr-variant-5-prime | USP16 | GRCh38.p7 | 21:29036349 | TTATGTCAGAAAACA[A/T]GCCAGCATTACAACT | 10600 |
rs2276517 | snp | A/G | 0.384401 | 0.210799 | intron-variant | USP16 | GRCh38.p7 | 21:29044499 | gatctcgccatttgc[A/G]ctccagcctgggcga | 10600 |
rs2409330 | snp | A/T | 0.284209 | 0.247648 | intron-variant | USP16 | GRCh38.p7 | 21:29035981 | TAGTGTTATTCTGTA[A/T]TTTAAAATATATGTA | 10600 |
rs2692624 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP16 | GRCh38.p7 | 21:29053320 | GTTCACTTTCCCCAC[A/G]AGAGAGTGCACGCTG | 10600 |
rs2776254 | snp | G/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29044274 | AGATAAACATTTTTG[G/T]TTTTTCTTACGTATC | 10600 |
rs2776256 | snp | G/T | 0 | 0 | intron-variant | USP16 | GRCh38.p7 | 21:29051957 | ATTTATTATACTTTT[G/T]TTTCTTGGCAGTAGT | 10600 |
rs2832152 | snp | A/G | 0.166506 | 0.235645 | intron-variant | USP16 | GRCh38.p7 | 21:29033307 | TTGTAATTTTCAAAA[A/G]TAGTATCAAATGTTA | 10600 |
rs2832153 | snp | A/C | 0.499722 | 0.0117779 | intron-variant | USP16 | GRCh38.p7 | 21:29036736 | AAGCATTTGTGATTC[A/C]TTCTAATGGTCAGAT | 10600 |
rs2832154 | snp | C/T | 0.301681 | 0.2446 | intron-variant | USP16 | GRCh38.p7 | 21:29037983 | TTGCTGCTTCTTTCA[C/T]GGAGCTTGCACTTGG | 10600 |
rs2832155 | snp | A/C | 0.477515 | 0.103619 | intron-variant | USP16 | GRCh38.p7 | 21:29038029 | GATAACCTCATATAG[A/C]AGCAAATACGTACCT | 10600 |
rs2832156 | snp | A/G | 0.154993 | 0.231244 | intron-variant | USP16 | GRCh38.p7 | 21:29042281 | TTAAATCTTGAAGAC[A/G]TTAAACAGTTTGATT | 10600 |
rs2832157 | snp | A/G | 0.305186 | 0.243833 | intron-variant | USP16 | GRCh38.p7 | 21:29043308 | TTTCAAATATTGTGG[A/G]AAAAAAAAGCTAATA | 10600 |
rs2853830 | snp | C/T | 0.419296 | 0.183954 | intron-variant | USP16 | GRCh38.p7 | 21:29044503 | ccaagatctcgccat[C/T]tgcactccagcctgg | 10600 |
rs3761337 | snp | C/G | 0.2462 | 0.249971 | upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29024157 | TAGCTGGGCGTGGTG[C/G]CGTGCGCCTGTAGTC | 10600 |
rs3887084 | snp | C/T | 0 | 0 | intron-variant | USP16 | GRCh38.p7 | 21:29050831 | atacagtggggagcc[C/T]tgaggagtttaaagc | 10600 |
rs4395323 | snp | C/T | 0.177182 | 0.23916 | intron-variant | USP16 | GRCh38.p7 | 21:29050713 | TAGTTCTAGAGTTTA[C/T]AGTACAAGGTTATAG | 10600 |
rs5843364 | in-del | -/T | 0.49962 | 0.0137727 | intron-variant | USP16 | GRCh38.p7 | 21:29044464 | TTTTTTTTTTTTTTT[-/T]GAGATGGTGTCTCAC | 10600 |
rs6516887 | snp | A/G | 0.316485 | 0.240998 | intron-variant | USP16 | GRCh38.p7 | 21:29029703 | ACATTGTGTAACTCC[A/G]TCATCTGGGGAGACA | 10600 |
rs7275909 | snp | A/C | 0.0414363 | 0.137845 | upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29024519 | CATTGACAACCAAAC[A/C]CCTAAACCCGAACAT | 10600 |
rs7276339 | snp | A/C | 0.00957816 | 0.0685371 | intron-variant | USP16 | GRCh38.p7 | 21:29040562 | TTTCTAAGGaaaata[A/C]aatttaaaatttaat | 10600 |
rs7277297 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant, upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29026613 | tcttgaacttctggc[C/T]tcaagccgtcctccc | 10600 |
rs7277402 | snp | G/T | 0.345679 | 0.230967 | intron-variant, upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29026562 | TTTTTTTTTTTTTTT[G/T]GTAGAGATAGAGTGT | 10600 |
rs7279398 | snp | G/T | 0.021333 | 0.101051 | intron-variant | USP16 | GRCh38.p7 | 21:29044716 | cctaccaaagtgctg[G/T]gattacagatgtgag | 10600 |
rs7279811 | snp | C/T | 0.0414363 | 0.137845 | intron-variant | USP16 | GRCh38.p7 | 21:29031926 | aaacaacacaccaat[C/T]gcaatcagatctcct | 10600 |
rs7280960 | snp | A/G | 0.220843 | 0.248294 | intron-variant | USP16 | GRCh38.p7 | 21:29034026 | TGTGAATAAGAGAAT[A/G]TGGGAGTTAACACTG | 10600 |
rs8128034 | snp | C/T | 0.250732 | 0.249999 | intron-variant | USP16 | GRCh38.p7 | 21:29033528 | TGAAGATATGTTTCT[C/T]AGCAGTGATCTGACT | 10600 |
rs8128151 | snp | G/T | 0.250732 | 0.249999 | intron-variant | USP16 | GRCh38.p7 | 21:29033442 | AAGTATATATTTAGC[G/T]GCAATGGAAACACGA | 10600 |
rs8128844 | snp | G/T | 0.0414363 | 0.137845 | intron-variant | USP16 | GRCh38.p7 | 21:29049530 | TTCTGGATGGCTGAA[G/T]CAGAAACATTGAGAA | 10600 |
rs8129928 | snp | A/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29051805 | actgcactcctgcct[A/G]ggtgacagagcaaga | 10600 |
rs8130040 | snp | A/C | | | intron-variant | USP16 | GRCh38.p7 | 21:29051798 | ttgcgtcactgcact[A/C]ctgcctaggtgacag | 10600 |
rs8133768 | snp | A/G | 0.477684 | 0.103247 | intron-variant, upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29027789 | ACATGCATAATATAC[A/G]TGGCTTAGTTATATT | 10600 |
rs8134780 | snp | A/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29029114 | tgctgatttggtagt[A/T]aaaaaaggttacctt | 10600 |
rs8134828 | snp | C/T | 0.0310518 | 0.120672 | intron-variant | USP16 | GRCh38.p7 | 21:29052092 | GAAGttcccaaactt[C/T]aatgtgtatgtggga | 10600 |
rs9305387 | snp | C/T | 0.155325 | 0.23138 | intron-variant | USP16 | GRCh38.p7 | 21:29031555 | gcagttttcctgcct[C/T]agtctccaagtagct | 10600 |
rs9305388 | snp | A/G | 0.165527 | 0.235296 | intron-variant | USP16 | GRCh38.p7 | 21:29031556 | cagttttcctgcctc[A/G]gtctccaagtagctg | 10600 |
rs9808746 | snp | C/G | 0.246769 | 0.249979 | intron-variant | USP16 | GRCh38.p7 | 21:29032413 | atttttgtatttttt[C/G]taaagatgcggtttt | 10600 |
rs11088105 | snp | C/G | | | upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29023785 | tttgtatttttagta[C/G]agacgggatttcacc | 10600 |
rs11299304 | in-del | -/T | 0.0256215 | 0.110247 | intron-variant | USP16 | GRCh38.p7 | 21:29032823 | CAATTTAATGTTTAG[-/T]TTTTTAAGAAACTGC | 10600 |
rs11909502 | snp | A/T | 0.0162398 | 0.0886349 | intron-variant, upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29026951 | AAAGTTTAGGGAGTG[A/T]GGTCCAGGAAACTGT | 10600 |
rs13051884 | snp | C/G | 0.021333 | 0.101051 | intron-variant, upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29026015 | TACTGGGGAAGTTCA[C/G]TGGAGAGGTTTATTT | 10600 |
rs13052178 | snp | C/T | 0.021333 | 0.101051 | intron-variant, upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29026424 | tcgggccactgcact[C/T]cggcctgggcgacag | 10600 |
rs16983655 | snp | A/G | 0.0225045 | 0.103662 | intron-variant | USP16 | GRCh38.p7 | 21:29049092 | CCCTCTTTTTAGTAC[A/G]ATTGGCATCTTACTT | 10600 |
rs16983662 | snp | A/G | 0.0345262 | 0.126772 | intron-variant | USP16 | GRCh38.p7 | 21:29051869 | GTTGCTGTGATGGGC[A/G]TAATGGAAGAGGCCG | 10600 |
rs17811387 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | USP16 | GRCh38.p7 | 21:29041534 | TTTGTTTTTAAAATA[C/T]CAAAGGAGTTCAGTC | 10600 |
rs28454471 | snp | A/C | 0.156319 | 0.231784 | intron-variant | USP16 | GRCh38.p7 | 21:29032901 | TACTAGCAGTGTATG[A/C]ATGATTCACTTTCAC | 10600 |
rs34265298 | in-del | -/C | | | upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29024616 | GGGGTGGTGGTGGCC[-/C]TAGCCACTTCCCATA | 10600 |
rs34338644 | snp | A/G | 0.49975 | 0.0111793 | intron-variant, upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29026835 | GATCAAAAGCACTAT[A/G]TAGTTATAACTTTAG | 10600 |
rs34383995 | in-del | -/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29029820 | ATGAAGTCTGAAAGA[-/T]CTTGAGTCTAAATTC | 10600 |
rs34755118 | in-del | -/C | | | intron-variant | USP16 | GRCh38.p7 | 21:29030044 | AGATGTTACCTCCCC[-/C]TGTGAAACTTTTGGT | 10600 |
rs34927375 | snp | A/G | 0.132066 | 0.220435 | intron-variant | USP16 | GRCh38.p7 | 21:29047812 | AATAGGATGTGGAGG[A/G]GCCATGGATTCCTAA | 10600 |
rs35013087 | snp | G/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29034323 | TTTTTTTTTTTTATT[G/T]TGAGATGGAGTTTTT | 10600 |
rs35019562 | in-del | -/C | | | intron-variant | USP16 | GRCh38.p7 | 21:29053632 | TTATAATAAAAACAG[-/C]AAGTGTCTCAGGCTG | 10600 |
rs35067147 | in-del | -/C | | | intron-variant | USP16 | GRCh38.p7 | 21:29036931 | ATTTATTTCATGTCC[-/C]ATGTTCTTGATTGTT | 10600 |
rs35358230 | in-del | -/G | 0.499997 | 0.00119808 | intron-variant | USP16 | GRCh38.p7 | 21:29037878 | GGCGTGAGCCACCAT[-/G]CCTGGCCAAAGAAAA | 10600 |
rs35528747 | in-del | -/T | | | upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29024376 | AAGCGTTCCCCCTTT[-/T]AGCTCCAAATATAAT | 10600 |
rs35628948 | in-del | -/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29039971 | TTGTAAGAGTCAGGG[-/G]AACATTGGTTGCATT | 10600 |
rs35788747 | in-del | -/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29046660 | ATGCCGTATACTTTT[-/T]ACCCAGAACCAACGA | 10600 |
rs35801969 | in-del | -/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29028123 | TTTTTTTTTTTTTTT[-/T]GAGAAAGAATCTCGC | 10600 |
rs35856856 | in-del | -/C | | | intron-variant, upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29026734 | ACCATTTTTTTTTCC[-/C]TGACTTTTCTCCTTG | 10600 |
rs55739028 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29027050 | CTCCCACATCGATTA[A/G]AGTGAGTTGGATTGG | 10600 |
rs55802924 | snp | A/G | 0 | 0 | intron-variant, upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29026901 | GTCAGGATTAGCCGA[A/G]CAATGGGGCCGAATT | 10600 |
rs55859573 | in-del | -/TTTTTTTT | | | downstream-variant-500B | USP16 | GRCh38.p7 | 21:29054623 | TTTTTTTTTTTTTTT[-/TTTTTTTT]GAGACGGAGTCTTGC | 10600 |
rs56050263 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29026882 | TGTTGAGGTGTAATA[A/G]AAAGTCAGGATTAGC | 10600 |
rs56256164 | snp | A/G | 0.0352966 | 0.128072 | intron-variant | USP16 | GRCh38.p7 | 21:29052080 | ATACATGTGATTGAA[A/G]TTCCCAAACTTTAAT | 10600 |
rs56404428 | snp | C/T | 0.267908 | 0.249358 | intron-variant | USP16 | GRCh38.p7 | 21:29052891 | TTCCAGAGGCTGAGG[C/T]GGGAGGATCACTTGA | 10600 |
rs56703875 | in-del | -/AAG | 0.0410537 | 0.137264 | intron-variant | USP16 | GRCh38.p7 | 21:29038273 | GAATAGACACTTAAG[-/AAG]TGTCAGAGTTGATTT | 10600 |
rs56763200 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29026453 | AGAGCAAGACTCCGT[C/T]TCAAAAAAAAAAAAA | 10600 |
rs56805614 | in-del | -/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29044464 | TTTTTTTTTTTTTTT[-/T]GAGATGGTGTCTCAC | 10600 |
rs57057123 | snp | C/G | 0.0418186 | 0.138422 | intron-variant | USP16 | GRCh38.p7 | 21:29038042 | AGAAGCAAATACGTA[C/G]CTACAGGTAGTGGTA | 10600 |
rs59182753 | snp | C/T | 0.289942 | 0.246789 | upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29023676 | AGTGATCTTGGCTCA[C/T]TGCAACCTCTGCCTC | 10600 |
rs59988733 | snp | A/G | 0.0482946 | 0.147699 | intron-variant | USP16 | GRCh38.p7 | 21:29034004 | TGTTTTTAGCTGGTC[A/G]TTGGTATGTGAATAA | 10600 |
rs60260312 | snp | A/G | 0.283421 | 0.247756 | intron-variant | USP16 | GRCh38.p7 | 21:29032075 | TCACAGGGATCTCTT[A/G]TGTTGCCCTTGTATA | 10600 |
rs60837311 | in-del | -/T | 0 | 0 | intron-variant, upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29026561 | TTTTTTTTTTTTTTT[-/T]TGTAGAGATAGAGTG | 10600 |
rs61735762 | snp | C/G | 0.00236077 | 0.0342755 | synonymous-codon | USP16 | GRCh38.p7 | 21:29046795 | AGTAAATATTAAATC[C/G]AACCATATTTCACAA | 10600 |
rs61735763 | snp | A/G | 0.0718857 | 0.175429 | synonymous-codon, utr-variant-5-prime | USP16 | GRCh38.p7 | 21:29034887 | GAAGCACTATCTGAC[A/G]CCAAGATCTGAACCT | 10600 |
rs61760206 | snp | C/T | 0.000777611 | 0.0197028 | missense | USP16 | GRCh38.p7 | 21:29046998 | ATGGTGCCTACCTAA[C/T]GGAAGGGAGCAATGG | 10600 |
rs62222369 | snp | C/T | 0.110519 | 0.207473 | intron-variant | USP16 | GRCh38.p7 | 21:29029407 | AACAGAGCAAGACTC[C/T]GTCTCAAAAAGAAAA | 10600 |
rs62222370 | snp | G/T | 0.0752113 | 0.178743 | intron-variant | USP16 | GRCh38.p7 | 21:29035014 | AATGTTTAAATATGT[G/T]TAAGAAGAAAGCAAT | 10600 |
rs62222371 | snp | C/T | 0.5 | 0 | intron-variant | USP16 | GRCh38.p7 | 21:29035150 | GTAACATAGAAGACT[C/T]AAGAATCTTTACCCC | 10600 |
rs62222372 | snp | C/T | 0.0752113 | 0.178743 | intron-variant | USP16 | GRCh38.p7 | 21:29037558 | CACCTGAGTAATTTA[C/T]TTCTATGTATCCAAA | 10600 |
rs62222373 | snp | C/T | 0.0752113 | 0.178743 | intron-variant | USP16 | GRCh38.p7 | 21:29045201 | GTTCCTCTGTTTTTA[C/T]GGAAACACATCAGAA | 10600 |
rs62222374 | snp | A/G | 0.0991586 | 0.199366 | intron-variant | USP16 | GRCh38.p7 | 21:29049851 | CAGGCATGTGCCATC[A/G]TGTCCAGCTGGGAAT | 10600 |
rs67919060 | in-del | -/GTGT | 0 | 0 | intron-variant | USP16 | GRCh38.p7 | 21:29048095 | TGTGTGTGTGTGTGT[-/GTGT]TTTGAGACAGAGTCC | 10600 |
rs71189336 | in-del | -/TT | | | intron-variant | USP16 | GRCh38.p7 | 21:29037603 | TTTTTTTTTTTTTTT[-/TT]GAGACAGGGTCTCAC | 10600 |
rs71319482 | snp | C/T | 0.5 | 0 | intron-variant | USP16 | GRCh38.p7 | 21:29029760 | TTGGCATGGGCATTT[C/T]CAGATTGCCCTTCAC | 10600 |
rs73192117 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | USP16 | GRCh38.p7 | 21:29028071 | TATTATTGTTATATT[A/T]TCTGCATTTTAATAT | 10600 |
rs73192118 | snp | C/G | 0.0792508 | 0.182605 | intron-variant | USP16 | GRCh38.p7 | 21:29028833 | ACTGTTACAGATTTA[C/G]GTAATCTTTAACTTT | 10600 |
rs73344758 | snp | A/C | 0.0134861 | 0.0810011 | intron-variant | USP16 | GRCh38.p7 | 21:29044844 | TTTCTCTATTGATTT[A/C]GGTTGTTTCTAGTAT | 10600 |
rs73344762 | snp | C/G | 0.021333 | 0.101051 | intron-variant | USP16 | GRCh38.p7 | 21:29048473 | ACCAAAATATTGTGT[C/G]TCTCCACAGTAATTC | 10600 |
rs73344764 | snp | A/G | 0.0345262 | 0.126772 | intron-variant | USP16 | GRCh38.p7 | 21:29049616 | CCAGGCTGGTGTGCA[A/G]TGACACGATCATGGC | 10600 |
rs73344766 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | USP16 | GRCh38.p7 | 21:29052545 | TCAGTTGCGTCCCAA[C/T]GGGTACCCTCCCATG | 10600 |
rs73901168 | snp | A/G | 0.0275645 | 0.114116 | intron-variant | USP16 | GRCh38.p7 | 21:29038934 | GCAGTTCTGTCAGGA[A/G]CATTGGTAGTATATG | 10600 |
rs73901169 | snp | C/T | 0.030665 | 0.119967 | intron-variant | USP16 | GRCh38.p7 | 21:29041004 | TTATTAATCATGGAG[C/T]CAACTTAGTTCTTAT | 10600 |
rs73901170 | snp | A/G | 0.0145532 | 0.0840522 | intron-variant | USP16 | GRCh38.p7 | 21:29047330 | ATAAAAGGTATTTTA[A/G]TGCTCTCACTGTAAG | 10600 |
rs74599828 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | USP16 | GRCh38.p7 | 21:29047506 | TACACTGTGACATCC[C/T]AGCAGCAGTTAAATG | 10600 |
rs74909163 | snp | A/T | 0.0205511 | 0.0992634 | intron-variant | USP16 | GRCh38.p7 | 21:29025107 | GCAGGGACTTCCCTA[A/T]GGGTTGGAGCTGGAT | 10600 |
rs74969104 | in-del | -/TTTTTTTTTTT | | | intron-variant | USP16 | GRCh38.p7 | 21:29037594 | CTTTTTTTTTTTTTT[-/TTTTTTTTTTT]GAGACAGGGTCTCAC | 10600 |
rs75530923 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | USP16 | GRCh38.p7 | 21:29053309 | GAAAGAATAAGCAGC[A/G]TGCACTCTCTCGTGG | 10600 |
rs75707840 | snp | A/G | 0.5 | 0 | synonymous-codon | USP16 | GRCh38.p7 | 21:29043482 | GGAGGATGAAGATCA[A/G]GATAGTGAGGAAGAA | 10600 |
rs75771109 | snp | C/T | 1.8261e-05 | 0.00302162 | intron-variant | USP16 | GRCh38.p7 | 21:29042004 | TGATAGACTTTTTTT[C/T]CTCCATAGATTATGA | 10600 |
rs75813013 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | USP16 | GRCh38.p7 | 21:29054247 | TAATGGCTGAAATAA[C/T]GATAAAAAAAGACTA | 10600 |
rs76618742 | snp | G/T | 0 | 0 | intron-variant, upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29026558 | TTTTTTTTTTTTTTT[G/T]TTTGGTAGAGATAGA | 10600 |
rs76722839 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | USP16 | GRCh38.p7 | 21:29045578 | TGTTTTTTTTTTTCT[C/T]TCAGTGAAACCTTGA | 10600 |
rs77526699 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | USP16 | GRCh38.p7 | 21:29025106 | GGCAGGGACTTCCCT[A/G]TGGGTTGGAGCTGGA | 10600 |
rs77898159 | snp | A/C | 0.0154538 | 0.0865337 | intron-variant | USP16 | GRCh38.p7 | 21:29034461 | GGGATTACAGATGTG[A/C]GCCACCACACCCGGC | 10600 |
rs78056639 | snp | G/T | 0.00234339 | 0.0341497 | synonymous-codon, utr-variant-5-prime | USP16 | GRCh38.p7 | 21:29039046 | ATTAGAAATAAACCT[G/T]GAGCCTCCAGGCCCT | 10600 |
rs78286027 | snp | A/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29045443 | TCTTTACTCTCTTCT[A/G]TATGTGTGGCTACCT | 10600 |
rs78302026 | in-del | -/A | 0.00156735 | 0.0279503 | intron-variant | USP16 | GRCh38.p7 | 21:29037487 | TTTCCCTTTAAAAAA[-/A]GCTGTCCTTTTCCTC | 10600 |
rs78364520 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP16 | GRCh38.p7 | 21:29044968 | GTTGATACTAATTGT[C/T]CTTCACAAAGGTTGC | 10600 |
rs78517954 | snp | A/C | | | missense, utr-variant-5-prime | USP16 | GRCh38.p7 | 21:29030678 | GAATGGAATATCTGC[A/C]AAGACTGTAAGACTG | 10600 |
rs78619921 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | USP16 | GRCh38.p7 | 21:29046306 | CGTGCCCAGCTAATT[C/T]TTATTTTTATTTTTT | 10600 |
rs78660279 | snp | A/G | 0.0607341 | 0.163335 | upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29023291 | AATAAAACAAAAATT[A/G]TCTCAGCAGTAAAAA | 10600 |
rs78753148 | snp | A/T | 0.0134861 | 0.0810011 | intron-variant | USP16 | GRCh38.p7 | 21:29032136 | TCTGCAGCCCCTGGC[A/T]ACTACCATTCTATTC | 10600 |
rs78869864 | snp | G/T | 0.5 | 0 | intron-variant | USP16 | GRCh38.p7 | 21:29045565 | TTTTCTTTCAGTTTG[G/T]TTTTTTTTTTCTCTC | 10600 |
rs79113181 | snp | A/C | 0.0154538 | 0.0865337 | intron-variant | USP16 | GRCh38.p7 | 21:29036139 | TCTTCTTCAGGAAAA[A/C]AGAATTTTTACGTTC | 10600 |
rs79245948 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29050572 | AACCATGCCTCAACT[A/G]TATTTAAAGAAGGAG | 10600 |
rs79511171 | snp | C/G | 0.5 | 0 | intron-variant | USP16 | GRCh38.p7 | 21:29046511 | GATCAGATTGTGAGA[C/G]TGAACTCTTCCTTAG | 10600 |
rs79541872 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | USP16 | GRCh38.p7 | 21:29049934 | CAAAAGCAAACCAAC[C/T]TGGAATCAGTTAGTG | 10600 |
rs79783820 | snp | A/G | 0.0162398 | 0.0886349 | upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29022671 | TCTGTTTTAAAATGC[A/G]TGGGGGCAAAAAGCC | 10600 |
rs79790480 | snp | G/T | 0 | 0 | intron-variant | USP16 | GRCh38.p7 | 21:29044462 | CTTTTTTTTTTTTTT[G/T]TTGAGATGGTGTCTC | 10600 |
rs79964727 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | USP16 | GRCh38.p7 | 21:29041565 | TTAGAGTTCACAAAA[C/T]AAGTTACATGCATTT | 10600 |
rs80043668 | snp | C/G | 0.0752113 | 0.178743 | upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29023000 | GGTCCGGTGGCTTAT[C/G]CCTGTAATCCAGCAT | 10600 |
rs80190648 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | USP16 | GRCh38.p7 | 21:29041122 | AGAAGCAACTAGGCA[C/T]GTGTGGCGCCTGAAA | 10600 |
rs80340505 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP16 | GRCh38.p7 | 21:29052538 | CCATGATTCAGTTGC[A/G]TCCCAACGGGTACCC | 10600 |
rs111333653 | snp | C/T | 0.5 | 0 | intron-variant | USP16 | GRCh38.p7 | 21:29049754 | TTTGTAGAGACAGAG[C/T]CTCACAGTGTTGCCC | 10600 |
rs111437197 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | USP16 | GRCh38.p7 | 21:29036792 | ATTAAATTAATTGGC[C/T]GACATACAGCATTTG | 10600 |
rs111604659 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | USP16 | GRCh38.p7 | 21:29042697 | AAGAACAGGGTAACT[A/G]CTTTAAAAACAAGGA | 10600 |
rs111690571 | snp | A/G | 0.5 | 0 | intron-variant | USP16 | GRCh38.p7 | 21:29043690 | TGGTTAGACATGTCT[A/G]TTATTTTAGATACAG | 10600 |
rs111772847 | snp | C/T | 0.5 | 0 | synonymous-codon | USP16 | GRCh38.p7 | 21:29047203 | CAATACTGATGAGTG[C/T]TCAATCCAACATTGT | 10600 |
rs111802082 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | USP16 | GRCh38.p7 | 21:29034532 | TGGTCAGGCTGGTCT[C/T]GAACTCCTGACCTCA | 10600 |
rs111946054 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | USP16 | GRCh38.p7 | 21:29034650 | TACTTGTTGACTTAA[A/G]TGTTCTCAGTTGCCT | 10600 |
rs112024808 | snp | G/T | 0.0349115 | 0.127424 | intron-variant | USP16 | GRCh38.p7 | 21:29028293 | ACAGCCAGCTAATTT[G/T]TTTTTTTTTTTTTAA | 10600 |
rs112054330 | snp | C/G | 0.0126979 | 0.078662 | intron-variant | USP16 | GRCh38.p7 | 21:29042774 | TGATTGGTTTCCATA[C/G]AGTGAAGTATTTTCC | 10600 |
rs112184186 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | USP16 | GRCh38.p7 | 21:29028627 | TTTTAGTAGAGACAG[A/G]GTTTCACCATGTTGA | 10600 |
rs112207711 | snp | A/G | 0 | 0 | intron-variant | USP16 | GRCh38.p7 | 21:29040959 | TAATACATGAATTAT[A/G]TTTGTTACTGTGAGT | 10600 |
rs112431177 | snp | C/G | | | intron-variant, upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29026271 | GACCAGCATGGCCAA[C/G]ATGGTGAAACCCCGT | 10600 |
rs112566907 | snp | A/T | 0.5 | 0 | intron-variant | USP16 | GRCh38.p7 | 21:29044630 | CTTTTGTATTTTTAG[A/T]AAAGACAGGTTTCGC | 10600 |
rs112631406 | snp | G/T | 0.5 | 0 | intron-variant | USP16 | GRCh38.p7 | 21:29053545 | TGAATTCAGTTATTT[G/T]GTATCTGAGCCAGGT | 10600 |
rs112703052 | snp | A/G | 0.0337553 | 0.125452 | intron-variant, upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29026349 | TAATCCCAGCTATTC[A/G]GGAGGCTGAGGCAGG | 10600 |
rs112841366 | snp | A/G | 0 | 0 | intron-variant | USP16 | GRCh38.p7 | 21:29044500 | CGCCCAGGCTGGAGT[A/G]CAAATGGCGAGATCT | 10600 |
rs112895849 | snp | A/G | 0.0055111 | 0.0522032 | intron-variant | USP16 | GRCh38.p7 | 21:29043406 | TTGTTTTTGACCTAT[A/G]TTATCTATATTTTAA | 10600 |
rs113072695 | snp | C/G/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29037878 | GGCGTGAGCCACCAT[C/G/T]CCTGGCCAAAGAAAA | 10600 |
rs113195607 | snp | C/T | 0 | 0 | intron-variant | USP16 | GRCh38.p7 | 21:29045984 | CATTACAGGCACGCC[C/T]GGCTAATTTTTGTAT | 10600 |
rs113245701 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29035030 | TAAGAAGAAAGCAAT[A/T]TAAAATTTTTGTAGT | 10600 |
rs113479300 | snp | C/T | 0.0916144 | 0.193427 | upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29023026 | AGCATTTTGGGAGGC[C/T]GAGGCAGGTGGATCA | 10600 |
rs113515348 | snp | C/G | 0.0429648 | 0.14013 | intron-variant | USP16 | GRCh38.p7 | 21:29044043 | GTTCAAGCAATTCTC[C/G]TGCCTCAGCCTCCTG | 10600 |
rs113745664 | snp | A/G | 0.5 | 0 | missense, utr-variant-5-prime | USP16 | GRCh38.p7 | 21:29034877 | AGCATGCCTTGAAGC[A/G]CTATCTGACGCCAAG | 10600 |
rs113931149 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | USP16 | GRCh38.p7 | 21:29037719 | GCCTCCAGAGTAGCT[A/G]GGACTACAGGCATGC | 10600 |
rs114224191 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | USP16 | GRCh38.p7 | 21:29045951 | GCTGGGATTACAGGC[A/G]CGCACCACCCATGTG | 10600 |
rs114251075 | snp | C/T | 0.00557542 | 0.0525036 | downstream-variant-500B | USP16 | GRCh38.p7 | 21:29054962 | ACAGCAGAATATAAA[C/T]GGGAGCAATGTTTCT | 10600 |
rs114353662 | snp | C/T | 0.0256215 | 0.110247 | upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29024546 | ACATCCGGCGCAAGC[C/T]GCACGCAGGCGCAGA | 10600 |
rs114720333 | snp | A/G | 0.00358779 | 0.0422022 | upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29023497 | TCCCCCGACCCCCAC[A/G]GTAGCGATTACTATC | 10600 |
rs115183462 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | USP16 | GRCh38.p7 | 21:29052567 | CCTCCCATGACATGT[A/G]GGAATTGTGGGAGCT | 10600 |
rs115384063 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | USP16 | GRCh38.p7 | 21:29030136 | TATTTAGCTGCCTTT[C/T]CTTCCAGAATGTGAG | 10600 |
rs115612236 | snp | C/T | 0.0325976 | 0.123435 | intron-variant | USP16 | GRCh38.p7 | 21:29035113 | AAGCTTTTACTTGGA[C/T]GTTTGCACAAGCACA | 10600 |
rs115835184 | snp | C/G | 0.0217236 | 0.101931 | intron-variant | USP16 | GRCh38.p7 | 21:29047758 | TCATACTGACAATTT[C/G]CCTTATCTCCCCATT | 10600 |
rs116214398 | snp | C/T | 0.021333 | 0.101051 | intron-variant | USP16 | GRCh38.p7 | 21:29051556 | GAATTTGGGGCTGGG[C/T]GTGGTGGCTTACGCC | 10600 |
rs116369748 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | USP16 | GRCh38.p7 | 21:29033433 | TCTTCTCCAAAGTAT[A/G]TATTTAGCGGCAATG | 10600 |
rs116679380 | snp | A/C | 0.0150606 | 0.0854603 | intron-variant | USP16 | GRCh38.p7 | 21:29031914 | ATATTGAGATTGAAA[A/C]AACACACCAATCGCA | 10600 |
rs116740943 | snp | A/T | 0.0162398 | 0.0886349 | intron-variant | USP16 | GRCh38.p7 | 21:29048449 | TATACTAAACTTTCA[A/T]CCTCATTAACCAAAA | 10600 |
rs116841526 | snp | A/C/G | 0.0287284 | 0.116357 | intron-variant | USP16 | GRCh38.p7 | 21:29035337 | AAAACAGATTTTTAC[A/C/G]TCTTAAAAATCATTT | 10600 |
rs116927602 | snp | A/G | 0.00414499 | 0.0453355 | intron-variant | USP16 | GRCh38.p7 | 21:29050222 | GTCCTTTAAAGTCAA[A/G]TTGTGGCTTACCTAA | 10600 |
rs117249152 | snp | A/G/T | 0.000643554 | 0.0179268 | missense, utr-variant-5-prime | USP16 | GRCh38.p7 | 21:29038353 | TTGTCACAAACACCA[A/G/T]TGCTTAGAGAACTAC | 10600 |
rs117530642 | snp | A/G | 0.0332853 | 0.124638 | intron-variant | USP16 | GRCh38.p7 | 21:29040559 | ATATTTCTAAGGAAA[A/G]TAAAATTTAAAATTT | 10600 |
rs117735878 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | USP16 | GRCh38.p7 | 21:29033033 | CTGTATGTTAGAAAA[G/T]ATACTGTTTACTTGT | 10600 |
rs117753456 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29024905 | GCACGTAACCCGGCT[A/G]CTTTCCGGTACTGCG | 10600 |
rs117880008 | snp | A/C | 0.0310518 | 0.120672 | intron-variant, upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29026163 | TTTTGGAGTGGAGTA[A/C]AAGAGAAGGACTTGG | 10600 |
rs117894989 | snp | A/G | 0.0236746 | 0.106192 | intron-variant | USP16 | GRCh38.p7 | 21:29035699 | GAATGGCATCTTTCA[A/G]TTGTAAAAGTTGTTA | 10600 |
rs117958954 | snp | A/C | 0.0345262 | 0.126772 | intron-variant | USP16 | GRCh38.p7 | 21:29046164 | TTTTTGAGACAGAGT[A/C]TTGCTCTGCCACCCA | 10600 |
rs118148152 | snp | C/G/T | 0.000523189 | 0.0161656 | intron-variant | USP16 | GRCh38.p7 | 21:29039588 | GCATGTTATGACCAT[C/G/T]GTATTTTATGATCTT | 10600 |
rs137890352 | snp | C/T | 0.00054351 | 0.016476 | synonymous-codon | USP16 | GRCh38.p7 | 21:29053909 | TGCCAAGGCAAGAAC[C/T]GCAAATAGTCATCTC | 10600 |
rs137921273 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP16 | GRCh38.p7 | 21:29050355 | CATTTTGAAGAATGG[A/G]TTATTTCAGTTCAAC | 10600 |
rs137983272 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29034493 | AATTTTTGTATTTTT[A/C]GTAGAGATGGGGTTT | 10600 |
rs138129745 | snp | G/T | 1.8242e-05 | 0.00302005 | missense | USP16 | GRCh38.p7 | 21:29040610 | TTTATTACTTTTAGA[G/T]AGTGAGTAAAGGAAT | 10600 |
rs138171167 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | USP16 | GRCh38.p7 | 21:29043116 | AGTCACTTAGAAAAT[A/G]TATTTGGAAATGGAC | 10600 |
rs138211287 | snp | C/T | 0.00111027 | 0.0235352 | intron-variant | USP16 | GRCh38.p7 | 21:29039166 | TAAAAAGTGAGTATC[C/T]ACTTCGATTGTGCTT | 10600 |
rs138330773 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | USP16 | GRCh38.p7 | 21:29028714 | TGCTGGGATTACAGG[C/T]GTGAGCCACCGCGCC | 10600 |
rs138359331 | snp | A/G | 0.000153988 | 0.00877328 | synonymous-codon | USP16 | GRCh38.p7 | 21:29042026 | AGATTATGAGAAGAA[A/G]AAATCAATGCCAAGT | 10600 |
rs138445383 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29050489 | ATGTTAAGGCTGGTG[A/G]ACATAGGTCAGGAGT | 10600 |
rs138515109 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | USP16 | GRCh38.p7 | 21:29029381 | TTGTGCCACTGCACT[C/G]CAGCCTGGGCAACAG | 10600 |
rs138599539 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | USP16 | GRCh38.p7 | 21:29025615 | TTTCCTATGGAGTCT[A/C]AGCTGCTGCAATCCT | 10600 |
rs138612814 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29038133 | GAGAATGCCCCACTG[A/G]GGTGATGAATAAGCT | 10600 |
rs138797032 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | USP16 | GRCh38.p7 | 21:29049325 | TGTGTTGCAAATTCC[A/G]AAAGTACTTTCAGTA | 10600 |
rs138869635 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP16 | GRCh38.p7 | 21:29044153 | TGGCCAGGCTGGTCT[C/G]AAACTCCTGACCTCA | 10600 |
rs139210093 | snp | A/G | 0.0127859 | 0.0789271 | utr-variant-5-prime, upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29024634 | GCCACTTCCCATAAT[A/G]CCGCGTTCCGGAAGT | 10600 |
rs139315892 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | USP16 | GRCh38.p7 | 21:29036122 | AGAGTTAATATGCAT[A/G]GTCTTCTTCAGGAAA | 10600 |
rs139489559 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP16 | GRCh38.p7 | 21:29053050 | CTCTAGTCCTGGGTG[C/T]GGTTGACTAAAATGG | 10600 |
rs139625942 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | USP16 | GRCh38.p7 | 21:29031465 | TTTTTTTGAGATGGG[A/G]TCTCACTCTGTCACC | 10600 |
rs139686893 | snp | C/G | 1.64855e-05 | 0.00287097 | missense | USP16 | GRCh38.p7 | 21:29054135 | AAGCTGTGCCTACAA[C/G]TAAAGTACTAAACTC | 10600 |
rs139766520 | snp | A/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29041109 | TGCTGTTCCATATAG[A/G]AGCAACTAGGCACGT | 10600 |
rs139938528 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | USP16 | GRCh38.p7 | 21:29046228 | AGTAACCTTGAACTT[C/T]TGGGCTCAAGTGATC | 10600 |
rs139997608 | in-del | -/GTA | 0.00142133 | 0.0266204 | intron-variant | USP16 | GRCh38.p7 | 21:29043377 | TTTTTTCACCAAATG[-/GTA]GTTGTAAAATTTTGT | 10600 |
rs140120110 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP16 | GRCh38.p7 | 21:29036718 | GTCTGCTGGGATAAC[A/G]TAAAGCATTTGTGAT | 10600 |
rs140152640 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP16 | GRCh38.p7 | 21:29040219 | GGCTGTAGAGAAGTT[C/G]AGTACCTAGTTTAAG | 10600 |
rs140228229 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29034421 | GAGTTCAAGCAGTTC[C/T]CCTGCCTCAGCCTCC | 10600 |
rs140357951 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | USP16 | GRCh38.p7 | 21:29048544 | TTTTGATTTCATCAG[C/T]AAGAATTTATGGACA | 10600 |
rs140436644 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29023474 | ATTTTTCTATAGCTA[C/T]CTGCAACTCCCCCGA | 10600 |
rs140500662 | snp | A/G | 0.0023933 | 0.0345097 | utr-variant-3-prime | USP16 | GRCh38.p7 | 21:29054439 | TACTTTGTGTTTAAT[A/G]TATCTGGGTGATGGA | 10600 |
rs140546730 | snp | C/G | 0.0221141 | 0.102801 | intron-variant | USP16 | GRCh38.p7 | 21:29028497 | CTGGAGTGCAGTAGT[C/G]TGATCTCAGCTCACT | 10600 |
rs140690927 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | USP16 | GRCh38.p7 | 21:29037128 | CTGGATGGCAATTTA[C/T]CTGTATCTATTTAAA | 10600 |
rs140697550 | snp | A/T | 0.0209421 | 0.100162 | intron-variant | USP16 | GRCh38.p7 | 21:29032076 | CACAGGGATCTCTTG[A/T]GTTGCCCTTGTATAA | 10600 |
rs140762644 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | USP16 | GRCh38.p7 | 21:29035065 | TTTAAAATACCATCA[C/T]TTTCACAAAGCTAAA | 10600 |
rs140788639 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP16 | GRCh38.p7 | 21:29037824 | CTCCTGGGCTTAAGC[C/T]GTCCACCCCCTTTGG | 10600 |
rs140935314 | snp | A/C | 1.6537e-05 | 0.00287545 | synonymous-codon | USP16 | GRCh38.p7 | 21:29046930 | AGATATGAAAAATAT[A/C]AACATGGATAATGAT | 10600 |
rs141111210 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29033341 | CATTTATTTTGTAAT[G/T]AAATGTTCAGTGGGA | 10600 |
rs141188052 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | USP16 | GRCh38.p7 | 21:29042305 | TTTGATTTATTTCCC[C/T]CAACCCAAAGTCCTC | 10600 |
rs141252862 | snp | A/T | 0.00249568 | 0.0352365 | synonymous-codon | USP16 | GRCh38.p7 | 21:29046963 | GGAGGTTTTAACATC[A/T]TCTCCCACTAGGAAT | 10600 |
rs141312121 | snp | A/C/G | 6.60965e-05 | 0.00574843 | missense, utr-variant-5-prime | USP16 | GRCh38.p7 | 21:29039501 | TGCGGTTTAAAGGCT[A/C/G]TCAGCAGCAAGACAG | 10600 |
rs141330180 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29038277 | AGACACTTAAGAAGT[A/G]TCAGAGTTGATTTGC | 10600 |
rs141403496 | snp | A/G | 0.000148501 | 0.0086156 | missense | USP16 | GRCh38.p7 | 21:29047102 | GAGATTCTGAATGAT[A/G]GTCATACTCCTGGAA | 10600 |
rs141561623 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | USP16 | GRCh38.p7 | 21:29052352 | GTTTACAGTTCCACA[A/T]GGCTGGGGAGGCCTC | 10600 |
rs141602051 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant, upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29025985 | GGGGACAAGATGACT[A/G]GAGCATACCATAAAT | 10600 |
rs141627967 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | USP16 | GRCh38.p7 | 21:29025583 | GCCTGCAGTAATTAA[C/T]AATTCGTCTTTCAAG | 10600 |
rs141732454 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29031153 | AAGGCAGCTCCCTTT[A/T]GTTGAGACTGATTCC | 10600 |
rs141911388 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | USP16 | GRCh38.p7 | 21:29039839 | TTGTACTAACCTATA[C/T]GAAGAGAGCTGCCAA | 10600 |
rs142067068 | snp | A/T | 0.0123036 | 0.0774623 | intron-variant | USP16 | GRCh38.p7 | 21:29049708 | GGGACTATAGGTGGC[A/T]ACCACCATGTCCAGC | 10600 |
rs142138861 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP16 | GRCh38.p7 | 21:29041660 | ACTAAGGAACTAGGC[C/T]GTCATTCAGCCTACT | 10600 |
rs142178023 | snp | A/C/T | 0.000231137 | 0.010748 | missense | USP16 | GRCh38.p7 | 21:29047234 | TTATATCAGTTCACC[A/C/T]GTAATGAGAAACTTC | 10600 |
rs142203110 | snp | C/G | 4.94303e-05 | 0.00497119 | missense | USP16 | GRCh38.p7 | 21:29054077 | ACAGATTTTGAAATG[C/G]AATCAAAAGGGCAGT | 10600 |
rs142450118 | snp | A/G | 0.00327544 | 0.040336 | intron-variant | USP16 | GRCh38.p7 | 21:29028022 | TATCTCTAAATGAAT[A/G]TGTTTTAAAATGTAA | 10600 |
rs142855561 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | USP16 | GRCh38.p7 | 21:29031646 | TTTTGCCATGTTGGC[C/T]AGGCTGGTCTCAAAC | 10600 |
rs142921353 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29034700 | CAAAATATTGATTCT[A/G]GAGTCTAACATTTTC | 10600 |
rs142929104 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29032668 | CTGTTTACCTGTCGA[A/G]TGACAACATCTGGGC | 10600 |
rs142950514 | snp | C/G | 1.65553e-05 | 0.00287705 | missense, utr-variant-5-prime | USP16 | GRCh38.p7 | 21:29030738 | GAAACAGAAGAAAAG[C/G]CTTCAGTTTGGCTGT | 10600 |
rs142991431 | in-del | -/ATGATTATGA | | | intron-variant | USP16 | GRCh38.p7 | 21:29034818 | ATGGCTTTGAGGTTT[-/ATGATTATGA]TTTTTTTAGGGCTGT | 10600 |
rs142993613 | snp | A/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29045036 | GATTTTGATTGGTAT[A/G]TTAGATGGAAAATAT | 10600 |
rs143002714 | snp | A/G | 0.021333 | 0.101051 | intron-variant | USP16 | GRCh38.p7 | 21:29035733 | TTGTCTGGCTAACAC[A/G]TTGAAACCCCATCTC | 10600 |
rs143073929 | snp | A/G | 1.6563e-05 | 0.00287771 | synonymous-codon | USP16 | GRCh38.p7 | 21:29047266 | AGATGCGAATAAACT[A/G]CTTTGTGAAGTATGC | 10600 |
rs143181337 | snp | A/T | 0.000230974 | 0.010744 | missense, utr-variant-5-prime | USP16 | GRCh38.p7 | 21:29038417 | AAATTGAACCACCTG[A/T]TTTGGCATTAACAGT | 10600 |
rs143207827 | in-del | -/TA | | | intron-variant | USP16 | GRCh38.p7 | 21:29047947 | ATATGTGTGTGTATG[-/TA]TATATATATATGTGT | 10600 |
rs143208735 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29047602 | GCATCCTGACACATA[C/G]TGGCTATTTTTTTCC | 10600 |
rs143493055 | snp | A/G | 1.70921e-05 | 0.00292331 | missense | USP16 | GRCh38.p7 | 21:29040643 | TTAAAGCATTTGGTA[A/G]TTCTACTGAAAAGTT | 10600 |
rs143698633 | snp | C/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29039283 | CTCTATATACAAAAG[C/G]CATAGTTTTTTTTCA | 10600 |
rs143780328 | snp | A/G | 1.66699e-05 | 0.00288698 | missense | USP16 | GRCh38.p7 | 21:29043556 | CTGGAACAAGTAAGC[A/G]CTTACAGAAAAAAGC | 10600 |
rs143799281 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | USP16 | GRCh38.p7 | 21:29040504 | AATTATTTAGTAAAT[A/G]TGGGGAGCTGTATCC | 10600 |
rs143810395 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29024842 | CGCTGGGAGAGCTCC[C/T]GTTTTCCGCCCCAAC | 10600 |
rs143845841 | snp | C/T | 0.00232039 | 0.0339825 | synonymous-codon, utr-variant-5-prime | USP16 | GRCh38.p7 | 21:29034935 | TTTGGACAACTGGAG[C/T]GTATGGTGAGTTTCA | 10600 |
rs144197751 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | USP16 | GRCh38.p7 | 21:29043995 | CAGAGTGCAGTGGCA[C/T]GATCTCTGCTCACTG | 10600 |
rs144253686 | snp | C/G/T | 4.95514e-05 | 0.00497732 | missense, synonymous-codon | USP16 | GRCh38.p7 | 21:29046876 | CCAAGCAAAAATGAT[C/G/T]GAAAGTGTAACTGAC | 10600 |
rs144317157 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | USP16 | GRCh38.p7 | 21:29051704 | GGCATGGTGGTGTGC[A/G]CCTGTAATCCCAGCT | 10600 |
rs144388105 | snp | A/G | 0.000266796 | 0.0115467 | missense | USP16 | GRCh38.p7 | 21:29043492 | GATCAAGATAGTGAG[A/G]AAGAAAAAGATAACG | 10600 |
rs144614405 | snp | A/G | 0.0298908 | 0.118541 | intron-variant | USP16 | GRCh38.p7 | 21:29029247 | TGAAACCCCGTCTCT[A/G]CTAAACATACAAAAA | 10600 |
rs144691396 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | USP16 | GRCh38.p7 | 21:29039361 | TGTTAATGGACTAAA[C/T]GGAAATTTGTAGAAA | 10600 |
rs144699960 | snp | A/G | 0.021333 | 0.101051 | intron-variant | USP16 | GRCh38.p7 | 21:29028153 | TTGAGAAAGAATCTC[A/G]CTCTGTTGCCCAGGC | 10600 |
rs144762579 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | USP16 | GRCh38.p7 | 21:29032422 | TTTTTTCTAAAGATG[C/T]GGTTTTGGTATACTG | 10600 |
rs144778465 | in-del | -/TA | | | intron-variant | USP16 | GRCh38.p7 | 21:29047970 | ATATGTGTGTGTATG[-/TA]TATATATATATAAGC | 10600 |
rs144779492 | in-del | -/A | 0.00517822 | 0.0506191 | upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29024560 | CGCACGCAGGCGCAG[-/A]ATTTACTAGCGTCAG | 10600 |
rs144907838 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29041205 | AAATTTAAATAGCCG[C/T]AAGTGACTAAGGGCA | 10600 |
rs145001972 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | USP16 | GRCh38.p7 | 21:29049117 | TTACTTTTATTTCAG[C/G]TTAAAAAAAGAAAAA | 10600 |
rs145047185 | snp | A/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29034320 | TTTTTTTTTTTTTTT[A/T]TTTTGAGATGGAGTT | 10600 |
rs145111205 | snp | G/T | 0.000693023 | 0.0186019 | missense | USP16 | GRCh38.p7 | 21:29047085 | CTGATGAAATAAATA[G/T]AGAGATTCTGAATGA | 10600 |
rs145151080 | snp | A/G | 0.00143506 | 0.0267483 | synonymous-codon, utr-variant-5-prime | USP16 | GRCh38.p7 | 21:29038352 | CTTGTCACAAACACC[A/G]GTGCTTAGAGAACTA | 10600 |
rs145151930 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | USP16 | GRCh38.p7 | 21:29033713 | TTTGGGATTTATAGA[A/C]CAGGTGAGAAAGGAT | 10600 |
rs145176938 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP16 | GRCh38.p7 | 21:29052790 | GCTCAGGAGTTTGAG[A/C]CCAGCCCAGGCAACA | 10600 |
rs145327890 | snp | A/T | 0.0162398 | 0.0886349 | intron-variant | USP16 | GRCh38.p7 | 21:29029535 | TTTCTTGGTGCAAGA[A/T]CATTGGACATAAAGC | 10600 |
rs145351174 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant, upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29027442 | TTTTTATTAGAGAAA[C/T]TATCAGTTTAATTTG | 10600 |
rs145368983 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | USP16 | GRCh38.p7 | 21:29036476 | ATACAGCTGAGTAAC[A/G]TTAGTTATGGTTGAT | 10600 |
rs145535662 | snp | A/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29053741 | GTGTAAACTTGTCTT[A/G]CCCATGACATCTGTG | 10600 |
rs145546478 | snp | A/C | 0.0126979 | 0.078662 | intron-variant | USP16 | GRCh38.p7 | 21:29053599 | TTACAGCTTTTCTAC[A/C]AGGGGAACAATGGTG | 10600 |
rs145760670 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | USP16 | GRCh38.p7 | 21:29032443 | TGGTATACTGCCCAG[G/T]CTGGTCTTGAACTCC | 10600 |
rs145924952 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | USP16 | GRCh38.p7 | 21:29025606 | CTTTCAAGTTTTCCT[A/T]TGGAGTCTAAGCTGC | 10600 |
rs146231617 | snp | A/G | 0.00398564 | 0.0444627 | upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29022699 | GCCTGCATTTCTGGA[A/G]CTTGGAGAAGAAAGC | 10600 |
rs146351448 | snp | A/G | 0.000671671 | 0.0183135 | missense | USP16 | GRCh38.p7 | 21:29046718 | CTTCATTTAAATGAT[A/G]TTTGTACTATTGACC | 10600 |
rs146370623 | snp | G/T | 0.0123036 | 0.0774623 | intron-variant | USP16 | GRCh38.p7 | 21:29044591 | TAGCTGGGATTACAG[G/T]CATGTGCCACCGTAC | 10600 |
rs146396744 | snp | C/T | 6.59076e-05 | 0.00574016 | synonymous-codon | USP16 | GRCh38.p7 | 21:29054106 | GTGGTTTCACATCAG[C/T]GACACACATGTGCAA | 10600 |
rs146502072 | in-del | -/TAGA | 0.0554779 | 0.157039 | intron-variant | USP16 | GRCh38.p7 | 21:29041928 | ATAAAATTTTAGAGT[-/TAGA]TAGGTAAGTAGTTTT | 10600 |
rs146577278 | in-del | -/TGAA | 0.0626846 | 0.165568 | intron-variant | USP16 | GRCh38.p7 | 21:29038471 | TGTAACTTTCCTCTC[-/TGAA]TGTGTGTTTTCTAAA | 10600 |
rs146674724 | snp | G/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29033744 | ATAAATATCAATAAC[G/T]TTAGTACAAGGTAAA | 10600 |
rs146777731 | snp | G/T | 0.00557542 | 0.0525036 | upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29024571 | CGCAGATTTACTAGC[G/T]TCAGAGCCGATGGTC | 10600 |
rs146797463 | snp | C/G | 8.25593e-05 | 0.0064244 | missense | USP16 | GRCh38.p7 | 21:29053824 | CAGAAGAAAATACAA[C/G]GGTACTCTATTCCTT | 10600 |
rs146808991 | snp | A/G | 0.000153988 | 0.00877328 | missense, utr-variant-5-prime | USP16 | GRCh38.p7 | 21:29036300 | ATAATGAGGTCCAGT[A/G]TTGTAGTTCAAACCA | 10600 |
rs146876888 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP16 | GRCh38.p7 | 21:29036934 | TTATTTCATGTCCAT[A/G]TTCTTGATTGTTTTA | 10600 |
rs146988310 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | USP16 | GRCh38.p7 | 21:29042598 | GTGGGGGGAAGCCTT[A/G]TTACTCTTTTTAAGT | 10600 |
rs146992992 | snp | C/T | 0.000462267 | 0.0151961 | synonymous-codon, utr-variant-5-prime | USP16 | GRCh38.p7 | 21:29039514 | CTATCAGCAGCAAGA[C/T]AGCCAGGAGCTGCTT | 10600 |
rs147167201 | snp | A/G | 8.70602e-05 | 0.00659716 | missense | USP16 | GRCh38.p7 | 21:29042013 | TTTTTTTCTCCATAG[A/G]TTATGAGAAGAAAAA | 10600 |
rs147251162 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29032064 | ATAGTTGAACATCAC[A/C]GGGATCTCTTGTGTT | 10600 |
rs147360376 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | USP16 | GRCh38.p7 | 21:29052531 | CCTGCTCCCATGATT[C/T]AGTTGCGTCCCAACG | 10600 |
rs147428760 | snp | A/T | 0.0268481 | 0.113104 | intron-variant | USP16 | GRCh38.p7 | 21:29034734 | TCAAGATTGTAAGAA[A/T]GGCAGAATTTCATGA | 10600 |
rs147587133 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | USP16 | GRCh38.p7 | 21:29052928 | GAGGCAGAGGTTGCA[C/T]TGAGCTGAGATCATG | 10600 |
rs147602567 | snp | A/G | 0.000676417 | 0.018378 | missense | USP16 | GRCh38.p7 | 21:29047223 | TCCAACATTGTTTAT[A/G]TCAGTTCACCCGTAA | 10600 |
rs147624751 | snp | A/G | 0.00156457 | 0.0279256 | missense | USP16 | GRCh38.p7 | 21:29047142 | ATGAGGTTGTAAATG[A/G]AGATCCAGAAACTGC | 10600 |
rs147656557 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29027783 | TGATAGACATGCATA[A/G]TATACGTGGCTTAGT | 10600 |
rs147692580 | snp | A/G | 0.0414363 | 0.137845 | upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29024057 | GCACGTTGGGAGGCC[A/G]AGGCGGGCGCATCAC | 10600 |
rs147762800 | snp | C/T | 1.79974e-05 | 0.00299973 | synonymous-codon | USP16 | GRCh38.p7 | 21:29046669 | ACTTTTTACCCAGAA[C/T]CAACGAAGACAACAA | 10600 |
rs147992331 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant, utr-variant-5-prime | USP16 | GRCh38.p7 | 21:29025025 | TTCCCCCGTGGGATC[A/G]GAGCAGTTAGAAGGG | 10600 |
rs148044346 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | USP16 | GRCh38.p7 | 21:29030110 | GTTTCGGAGATTCTT[A/G]TACATTAATTTATTT | 10600 |
rs148081936 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | USP16 | GRCh38.p7 | 21:29039639 | TCATTTGATATCTTA[C/T]GAGTTAAAACAATGA | 10600 |
rs148502169 | in-del | -/GG | | | intron-variant | USP16 | GRCh38.p7 | 21:29038109 | TAGCTACTTCTGATT[-/GG]GTGGTGGGAGAATGC | 10600 |
rs148519682 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29027396 | GGAAATTTTCTAACT[C/G]CCTTCAGGAGGTTGT | 10600 |
rs148522104 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP16 | GRCh38.p7 | 21:29032522 | TAGGTGTGAGCCACC[A/G]TGCCCAGCCAGGATT | 10600 |
rs148617415 | snp | C/T | 0.000100388 | 0.00708407 | synonymous-codon, upstream-variant-2KB, utr-variant-5-prime | USP16 | GRCh38.p7 | 21:29027952 | AAAAACTGTTCCAAT[C/T]GATGATTCCTCTGAA | 10600 |
rs148801838 | snp | A/C | 0.0252325 | 0.109451 | intron-variant | USP16 | GRCh38.p7 | 21:29051997 | GGTTTGGGGCATGGC[A/C]GGTACATTATAGGAT | 10600 |
rs148804242 | snp | G/T | 1.66651e-05 | 0.00288657 | stop-gained | USP16 | GRCh38.p7 | 21:29043495 | CAAGATAGTGAGGAA[G/T]AAAAAGATAACGACA | 10600 |
rs148908368 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP16 | GRCh38.p7 | 21:29053699 | ATTTCTGCACTCTCA[A/G]AGTAATGGTTAAAGA | 10600 |
rs149014491 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29024742 | CCCAGCCCAAAGGCC[C/T]ATGAGGGGATGCAGT | 10600 |
rs149028933 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | USP16 | GRCh38.p7 | 21:29041429 | GTAAAATTATGGCTT[G/T]TAGTTATATTAAACT | 10600 |
rs149141484 | snp | A/G | 1.64972e-05 | 0.00287199 | missense, utr-variant-5-prime | USP16 | GRCh38.p7 | 21:29038362 | ACACCAGTGCTTAGA[A/G]AACTACTAAAAGAAG | 10600 |
rs149208010 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | USP16 | GRCh38.p7 | 21:29028841 | AGATTTAGGTAATCT[C/T]TAACTTTTTAGTATT | 10600 |
rs149255317 | snp | C/T | 0.00133571 | 0.0258084 | missense | USP16 | GRCh38.p7 | 21:29042079 | GTGAACTAACTAGTA[C/T]GATCATGTGTGATCA | 10600 |
rs149473061 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP16 | GRCh38.p7 | 21:29034500 | GTATTTTTAGTAGAG[A/G]TGGGGTTTCACCATG | 10600 |
rs149499001 | in-del | -/CTTT | 0.0158469 | 0.0875917 | upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29022617 | ATCAGGGGGAAGAGG[-/CTTT]CTGACAGGAAGCACG | 10600 |
rs149560995 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | USP16 | GRCh38.p7 | 21:29043861 | AATTAACTTAATTTT[C/T]GAGTTAATATTATTG | 10600 |
rs149615502 | snp | C/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29051568 | GGGCGTGGTGGCTTA[C/T]GCCTGTAATGCCAAC | 10600 |
rs149669301 | snp | A/T | 0.000747119 | 0.0193132 | intron-variant | USP16 | GRCh38.p7 | 21:29046653 | TTTTTTGATGCCGTA[A/T]ACTTTTTACCCAGAA | 10600 |
rs149721151 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | USP16 | GRCh38.p7 | 21:29053570 | CCAGGTAACTGCATC[A/G]AGTGGCCTGTGGCTT | 10600 |
rs149965549 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29026833 | AAGATCAAAAGCACT[A/G]TATAGTTATAACTTT | 10600 |
rs149982041 | in-del | -/TG | 0.00039004 | 0.0139595 | intron-variant | USP16 | GRCh38.p7 | 21:29038474 | ACTTTCCTCTCTGAA[-/TG]TGTGTGTTTTCTAAA | 10600 |
rs150003035 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | USP16 | GRCh38.p7 | 21:29036150 | AAAACAGAATTTTTA[C/T]GTTCGGTTTCTTTAA | 10600 |
rs150054074 | snp | C/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29041203 | TTAAATTTAAATAGC[C/T]GTAAGTGACTAAGGG | 10600 |
rs150108349 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29038129 | GTGGGAGAATGCCCC[A/G]CTGAGGTGATGAATA | 10600 |
rs150163490 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | USP16 | GRCh38.p7 | 21:29042834 | ATTTAAGACTAATCA[C/T]GAATCCCTTGCACAC | 10600 |
rs150549667 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29031313 | GCTCACAGTTATTAC[C/T]GTGGTACTAAAGTCA | 10600 |
rs150637933 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | USP16 | GRCh38.p7 | 21:29040100 | CTTATTTTTATGCCA[A/G]TCACTGTTTTCAGTG | 10600 |
rs150692145 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | USP16 | GRCh38.p7 | 21:29045670 | ATAACATTTGACTGC[C/T]TGGGTTTAACAGTCT | 10600 |
rs150695069 | snp | C/G | 6.58935e-05 | 0.00573955 | synonymous-codon, utr-variant-5-prime | USP16 | GRCh38.p7 | 21:29034869 | TCAGGAGCAGCATGC[C/G]TTGAAGCACTATCTG | 10600 |
rs150814396 | snp | A/C | 0.0209421 | 0.100162 | intron-variant | USP16 | GRCh38.p7 | 21:29035917 | AGCGAGACTCCGTCT[A/C]AAAAAAAACCAAAAA | 10600 |
rs150921923 | snp | C/T | 1.65113e-05 | 0.00287322 | missense, utr-variant-5-prime | USP16 | GRCh38.p7 | 21:29037366 | AAAAGAAGGAAAACA[C/T]GGCTAAAGAGAATCC | 10600 |
rs151074601 | snp | A/G | 0.00219615 | 0.0330643 | missense | USP16 | GRCh38.p7 | 21:29046907 | AATCAAAAATCCACA[A/G]AGGAAGTAGATATGA | 10600 |
rs151222202 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | USP16 | GRCh38.p7 | 21:29048454 | TAAACTTTCAACCTC[A/G]TTAACCAAAATATTG | 10600 |
rs151255018 | snp | A/G | 0.00279162 | 0.0372561 | upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29023167 | GCCACTGGGGAGGGT[A/G]AGGTGGGAGAATCGG | 10600 |
rs180736459 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | USP16 | GRCh38.p7 | 21:29051703 | AGGCATGGTGGTGTG[C/T]GCCTGTAATCCCAGC | 10600 |
rs180752763 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29043248 | TTCTCATTATGTGAA[G/T]ATTGCTTTCTAGTGT | 10600 |
rs180763932 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | USP16 | GRCh38.p7 | 21:29034399 | CTCACTGCAACCTCC[A/G]CCTCCTGAGTTCAAG | 10600 |
rs180903398 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29030524 | ATGTGAATCGAGGGT[A/G]AGTTTTGAGATTAAC | 10600 |
rs181414004 | snp | C/T | 0 | 0 | intron-variant | USP16 | GRCh38.p7 | 21:29044985 | TTCACAAAGGTTGCT[C/T]CTGACCCTTGACAGC | 10600 |
rs181430580 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | USP16 | GRCh38.p7 | 21:29051038 | TATTTCAGGAGGTAG[A/C]ATTAACCAGACTTAA | 10600 |
rs181521483 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29030099 | TGCTATACCATGTTT[C/T]GGAGATTCTTATACA | 10600 |
rs181536872 | snp | A/G | 0.000412422 | 0.0143541 | missense | USP16 | GRCh38.p7 | 21:29047214 | AGTGTTCAATCCAAC[A/G]TTGTTTATATCAGTT | 10600 |
rs181598513 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP16 | GRCh38.p7 | 21:29033878 | GGAGGTGGCTTTTGA[A/G]CAAGATCTTGAAGAG | 10600 |
rs181639163 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP16 | GRCh38.p7 | 21:29033366 | GTGGGATAAATTAAG[C/T]GAATAGTGTTTGGGA | 10600 |
rs181750901 | snp | G/T | 5.30509e-05 | 0.00515001 | intron-variant | USP16 | GRCh38.p7 | 21:29027990 | GTATATTTCATTGAT[G/T]GAATCTTTAATGTTT | 10600 |
rs181969699 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | USP16 | GRCh38.p7 | 21:29044149 | TTGTTGGCCAGGCTG[A/G]TCTCAAACTCCTGAC | 10600 |
rs182005822 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | USP16 | GRCh38.p7 | 21:29038218 | TTTCATTTTCCAAGT[A/G]TAGAGTTTTCAGTGT | 10600 |
rs182134920 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29035926 | CCGTCTCAAAAAAAA[A/C]CAAAAAACAAAACAA | 10600 |
rs182147097 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29053538 | GGCAAGTTGAATTCA[A/G]TTATTTGGTATCTGA | 10600 |
rs182302061 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29024538 | AAACCCGAACATCCG[A/G]CGCAAGCCGCACGCA | 10600 |
rs182318763 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29039370 | ACTAAACGGAAATTT[A/G]TAGAAACCAGAACTC | 10600 |
rs182328965 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29023387 | TTAAACTCCTTTTAT[A/C]TGATTAGTAAGGATG | 10600 |
rs182334213 | snp | A/G | 1.6507e-05 | 0.00287284 | missense | USP16 | GRCh38.p7 | 21:29047082 | ATCCTGATGAAATAA[A/G]TATAGAGATTCTGAA | 10600 |
rs182461985 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP16 | GRCh38.p7 | 21:29045281 | AGAGTAGCCTCACAG[A/G]GGCTGTTCTTTCAGT | 10600 |
rs182588973 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | USP16 | GRCh38.p7 | 21:29029869 | GTTATGTGGGTACTA[A/C]ATCTTAGTTTTCTCA | 10600 |
rs182691085 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP16 | GRCh38.p7 | 21:29028695 | CTTCCTCAGCATCCC[A/G]AAGTGCTGGGATTAC | 10600 |
rs182754050 | snp | G/T | 1.65154e-05 | 0.00287358 | missense | USP16 | GRCh38.p7 | 21:29048807 | AAAGCAGATGCTAAT[G/T]TCTCTTGCTCCTCCT | 10600 |
rs182786188 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | USP16 | GRCh38.p7 | 21:29031527 | CATGGCAGCCTCCAC[C/T]TCCCAGGTTCAAGCA | 10600 |
rs182811362 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | USP16 | GRCh38.p7 | 21:29028083 | ATTATCTGCATTTTA[A/G]TATAATGTTTGTATC | 10600 |
rs182890396 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29052175 | GCATGTTTAATGTAA[A/T]CTCTCAGGTGATGCT | 10600 |
rs182901958 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | USP16 | GRCh38.p7 | 21:29029034 | CAGGCCCCCTATTAG[C/T]GTAGTAAAGTGCCCA | 10600 |
rs183147515 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29052687 | TTGGAGATCCTGTTA[C/G]GTTAAAGAGTACAGA | 10600 |
rs183314668 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | USP16 | GRCh38.p7 | 21:29038797 | TTGGCTCTTTCAATT[C/G]TTAGGTAGTAAGTGT | 10600 |
rs183397020 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29035405 | TTTTGAGACGGAATC[G/T]TTCTGTCGCCCAGGC | 10600 |
rs183429237 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | USP16 | GRCh38.p7 | 21:29031112 | TTGGATGTGGCCTGC[A/C]CCTAGAGCAGGAAGT | 10600 |
rs183555445 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29024126 | AACCCCGTCTCTACT[A/T]AAAATACAAAAATTT | 10600 |
rs183982427 | snp | A/G | 0.00795532 | 0.062565 | intron-variant, upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29026345 | TCTGTAATCCCAGCT[A/G]TTCGGGAGGCTGAGG | 10600 |
rs184033684 | snp | C/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29046207 | GTGTGCATGATCATA[C/T]CTCACAGTAACCTTG | 10600 |
rs184038565 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29048298 | ACGTTGGCCAGGGTG[A/G]TCTCAAACTCCTAAC | 10600 |
rs184092493 | snp | A/T | 0.000149903 | 0.00865614 | intron-variant | USP16 | GRCh38.p7 | 21:29046652 | ATTTTTTGATGCCGT[A/T]TACTTTTTACCCAGA | 10600 |
rs184113953 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | USP16 | GRCh38.p7 | 21:29029195 | AAGGCGGGCAGATCA[C/T]GAGGTCAGGAGATCG | 10600 |
rs184193106 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29040167 | TTCTGTGAGGTGGAT[A/G]CTGTGATTTTTTCCT | 10600 |
rs184283983 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP16 | GRCh38.p7 | 21:29029344 | CGTGAACCTGGGAGG[C/T]GGAGCTTGCAGTGAG | 10600 |
rs184386064 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29033459 | CAATGGAAACACGAC[C/T]GGTTGTTGTACTGTG | 10600 |
rs184741173 | snp | A/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29032373 | AGTAGCTGGGACTAC[A/T]CCTGCATGCCACCAC | 10600 |
rs184871057 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | USP16 | GRCh38.p7 | 21:29029922 | TCTTCTAGGGTGATT[G/T]TAAGGATTAAATGGG | 10600 |
rs184881299 | snp | G/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29049364 | ACGTTTTGCCTCTTG[G/T]GGTTGGTATGGGCTT | 10600 |
rs184885878 | snp | C/T | 0.000461544 | 0.0151842 | synonymous-codon | USP16 | GRCh38.p7 | 21:29047194 | GGAAGTTTTCAATAC[C/T]GATGAGTGTTCAATC | 10600 |
rs184890629 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP16 | GRCh38.p7 | 21:29037988 | GCTTCTTTCATGGAG[C/T]TTGCACTTGGGTGGA | 10600 |
rs184906177 | snp | A/G | 0.00557542 | 0.0525036 | downstream-variant-500B | USP16 | GRCh38.p7 | 21:29054762 | GGACTACAGGCGCCC[A/G]CCACCACGCCCAGCT | 10600 |
rs184927816 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29022648 | ACGTGGTACAATGAC[C/T]CTAAGGCTCTGTTTT | 10600 |
rs185001187 | snp | C/T | 0.00113968 | 0.0238441 | intron-variant | USP16 | GRCh38.p7 | 21:29037228 | GTATACTTCTGCATT[C/T]GATATGACTGTATTA | 10600 |
rs185016043 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29033066 | TTGAAAGGTTTAATT[G/T]TAACCTTTTAAATAC | 10600 |
rs185033793 | snp | G/T | 6.78081e-05 | 0.00582232 | intron-variant | USP16 | GRCh38.p7 | 21:29050073 | GAAAAGAAGTCAATC[G/T]GTTATGCTTCTCTTT | 10600 |
rs185038350 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | USP16 | GRCh38.p7 | 21:29041600 | TCCCAGTTTGCTACT[C/G]TGGTATCTTTTATCA | 10600 |
rs185154856 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29026082 | AGAGCTTCCAAGATT[A/G]GTAAGATTTAGATAG | 10600 |
rs185548585 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29036141 | TTCTTCAGGAAAACA[C/G]AATTTTTACGTTCGG | 10600 |
rs185636147 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | USP16 | GRCh38.p7 | 21:29028167 | CGCTCTGTTGCCCAG[G/T]CTGGAGTGCAGTGGT | 10600 |
rs185651949 | snp | A/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29045080 | TTTTATTTTACATTT[A/G]TTTTAATATAAATTA | 10600 |
rs185759118 | snp | A/C | | | upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29024397 | CAAATATAATGTGTT[A/C]CAGAAAGGTAACCAT | 10600 |
rs185766550 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | USP16 | GRCh38.p7 | 21:29043302 | ATCTATTTTCAAATA[C/T]TGTGGAAAAAAAAAG | 10600 |
rs185776381 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | USP16 | GRCh38.p7 | 21:29030200 | TTTGGGCTCCTGAGC[A/G]TCTAGCACAGTGCCT | 10600 |
rs185787914 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29047847 | TTTTAGTAGAATTGT[G/T]GAAACATTTTAAAAT | 10600 |
rs185905412 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29030571 | TGACCTTATATATTC[C/T]TTGTCTATTATTTGT | 10600 |
rs185906305 | snp | C/T | 0.00162099 | 0.028423 | intron-variant | USP16 | GRCh38.p7 | 21:29028009 | TCTTTAATGTTTATA[C/T]CTCTAAATGAATATG | 10600 |
rs186040364 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | USP16 | GRCh38.p7 | 21:29052227 | ACATTTTGAATAGCA[A/G]TGGTCTAGACTGCAT | 10600 |
rs186137878 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29048043 | ATATCAGCTCAGAGA[C/T]GATACGTGTGTGTGT | 10600 |
rs186313220 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | USP16 | GRCh38.p7 | 21:29052077 | GTGATACATGTGATT[A/G]AAGTTCCCAAACTTT | 10600 |
rs186323427 | snp | A/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29033966 | TGTGAACAAAATTGC[A/G]TAGTTGTGAAAAGCG | 10600 |
rs186358439 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29034718 | GTCTAACATTTTCTT[C/T]TCAAGATTGTAAGAA | 10600 |
rs186439850 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | USP16 | GRCh38.p7 | 21:29051514 | GTGAGGACACCACAA[A/C/G]GGATCTCAAAGAATC | 10600 |
rs186559755 | snp | G/T | 0.00795532 | 0.062565 | intron-variant | USP16 | GRCh38.p7 | 21:29044471 | TTTTTTTTTGAGATG[G/T]TGTCTCACTCTGTCG | 10600 |
rs186609236 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29038801 | CTCTTTCAATTCTTA[A/G]GTAGTAAGTGTTCCA | 10600 |
rs186928406 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29029227 | GACCATCCTGGCTAA[C/T]ACGGTGAAACCCCGT | 10600 |
rs186964543 | snp | C/T | | | upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29024582 | TAGCGTCAGAGCCGA[C/T]GGTCCCGGGAGGTGG | 10600 |
rs187041225 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP16 | GRCh38.p7 | 21:29048983 | TTAACTGTAATGTCA[A/G]TGAAGTCAGAAAGGG | 10600 |
rs187128572 | snp | A/C/G | 0.000965356 | 0.021949 | intron-variant | USP16 | GRCh38.p7 | 21:29038291 | TGTCAGAGTTGATTT[A/C/G]CCTTTAAATAATTTT | 10600 |
rs187155386 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | USP16 | GRCh38.p7 | 21:29035114 | AGCTTTTACTTGGAC[A/G]TTTGCACAAGCACAA | 10600 |
rs187323496 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29026574 | TTTGGTAGAGATAGA[A/G]TGTCGCTTTGTTGCC | 10600 |
rs187356790 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29023803 | ACGGGATTTCACCAC[A/G]TTGGCCAGGCTGGTC | 10600 |
rs187511651 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | USP16 | GRCh38.p7 | 21:29046301 | ACCAACGTGCCCAGC[C/T]AATTTTTATTTTTAT | 10600 |
rs187535291 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | USP16 | GRCh38.p7 | 21:29029067 | TCCCTGAACCTTCAT[C/T]GGCACTGGTTAGTAT | 10600 |
rs187679745 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29048362 | TCCTGGGATTACAGC[A/G]TGAGCCATCGCACCC | 10600 |
rs187707572 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29031119 | TGGCCTGCCCCTAGA[A/G]CAGGAAGTAACCTTG | 10600 |
rs187749880 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | USP16 | GRCh38.p7 | 21:29049602 | TCTTGTTCTGTCACC[C/G]AGGCTGGTGTGCAAT | 10600 |
rs187887510 | snp | C/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29035562 | TATTTTTAGTAGAGA[C/T]GGGGTTTCACCATGT | 10600 |
rs187932099 | snp | A/G | 0.000399281 | 0.0141238 | missense | USP16 | GRCh38.p7 | 21:29054107 | TGGTTTCACATCAGC[A/G]ACACACATGTGCAAG | 10600 |
rs187939417 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29035938 | AAACCAAAAAACAAA[A/G]CAAACAAAAAAAAGT | 10600 |
rs188014580 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | USP16 | GRCh38.p7 | 21:29031731 | GGCGTGAGCCACTGC[A/G]CCCAGCCAGGATTTT | 10600 |
rs188024044 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | USP16 | GRCh38.p7 | 21:29032685 | GACAACATCTGGGCT[A/G]ATCCCATTTTTTGGT | 10600 |
rs188141315 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | USP16 | GRCh38.p7 | 21:29038207 | CATCTGTAACTTTTC[A/G]TTTTCCAAGTATAGA | 10600 |
rs188188156 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | USP16 | GRCh38.p7 | 21:29053103 | GAATCATAGATGGAC[A/G]GAGAAGTACTAAGTT | 10600 |
rs188283353 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP16 | GRCh38.p7 | 21:29043171 | TATCTAATAAATTTC[A/G]TTATATTTCTATTAC | 10600 |
rs188318295 | snp | A/T | | | intron-variant, upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29026421 | AGATCGGGCCACTGC[A/T]CTCCGGCCTGGGCGA | 10600 |
rs188555611 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | USP16 | GRCh38.p7 | 21:29041761 | ACTTCCCACTGACTA[C/G]ATCTTGGATAAGGAC | 10600 |
rs188589534 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29026284 | AAGATGGTGAAACCC[C/T]GTCTCTACTAAAAAT | 10600 |
rs188693324 | snp | A/G | 0.00305197 | 0.0389445 | intron-variant | USP16 | GRCh38.p7 | 21:29040583 | AAAATTTAATAGTAT[A/G]TATATATCCATTTTA | 10600 |
rs188849191 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29028945 | CATAATTTTTGAATC[A/G]AAGGGTGTAAACATT | 10600 |
rs188956304 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | USP16 | GRCh38.p7 | 21:29025374 | ATTTTGTATGGAGTC[C/T]TGCGAAGAGTCATTT | 10600 |
rs189117961 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP16 | GRCh38.p7 | 21:29045310 | GTTCTTTCTGTTACA[A/G]CCAGAAATGCCTTTG | 10600 |
rs189200031 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | USP16 | GRCh38.p7 | 21:29030081 | AGCCTTCTCTGCTTG[G/T]GCTGCTATACCATGT | 10600 |
rs189217773 | snp | A/C | 1.64969e-05 | 0.00287196 | missense | USP16 | GRCh38.p7 | 21:29047212 | TGAGTGTTCAATCCA[A/C]CATTGTTTATATCAG | 10600 |
rs189284062 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | USP16 | GRCh38.p7 | 21:29051596 | AACACTTTGGGAGGC[C/T]GAGGCGGGTGGATCA | 10600 |
rs189341842 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29023180 | GTGAGGTGGGAGAAT[C/T]GGGAGGTGGAGGTTG | 10600 |
rs189342709 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | USP16 | GRCh38.p7 | 21:29033224 | CACTAGATACCTTTG[A/G]CACTGTTAGCTAATG | 10600 |
rs189358054 | snp | A/C | 3.34913e-05 | 0.00409201 | intron-variant | USP16 | GRCh38.p7 | 21:29050085 | ATCTGTTATGCTTCT[A/C]TTTTAGGCTGGTTTT | 10600 |
rs189459260 | snp | C/T | 0.000263983 | 0.0114857 | synonymous-codon, utr-variant-5-prime | USP16 | GRCh38.p7 | 21:29037409 | TCCTTGCCAAATAAC[C/T]GTGAAAGGACTCAGT | 10600 |
rs189596399 | snp | A/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29033460 | AATGGAAACACGACC[A/G]GTTGTTGTACTGTGA | 10600 |
rs189861489 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29050588 | TATTTAAAGAAGGAG[C/T]AAAAGTATGATGAAT | 10600 |
rs189964763 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP16 | GRCh38.p7 | 21:29045169 | GCTTATATTCTTTTC[C/T]TATTTTTTATTCATG | 10600 |
rs190072910 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29038948 | AACATTGGTAGTATA[A/T]GTTAACTAATTAGAT | 10600 |
rs190078830 | snp | A/C | 0.000798403 | 0.0199641 | upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29024436 | CTCCAAGGCTCAGAC[A/C]ACCACCGGATGCCCA | 10600 |
rs190108174 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29047915 | AAAGTAAGCCTGTGT[G/T]TGTGTGTATGTATCT | 10600 |
rs190118861 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | USP16 | GRCh38.p7 | 21:29054834 | AGCCAGGATGGTCTC[A/G]ATCTCCTGACCTCGT | 10600 |
rs190236434 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29043828 | GCATTGCTTGTAACA[A/G]GTATTTGTAGTAAGT | 10600 |
rs190391275 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29029400 | CCTGGGCAACAGAGC[A/G]AGACTCCGTCTCAAA | 10600 |
rs190407505 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29037028 | GAGATTTATACCAAA[C/G]CACATACTGTTTGGT | 10600 |
rs190497541 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29026994 | ATCAAGAGAGTGATA[C/T]GATAAAAATGGCATA | 10600 |
rs190576609 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | USP16 | GRCh38.p7 | 21:29048368 | GATTACAGCGTGAGC[C/T]ATCGCACCCAGCCTA | 10600 |
rs190610213 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29031292 | ATCACAGTATCTACT[C/T]TACCAGCTCACAGTT | 10600 |
rs190635870 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | USP16 | GRCh38.p7 | 21:29044774 | CTTTCTTTCTTTCTT[C/T]TTTTTAACAGTTGCA | 10600 |
rs190721771 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29052170 | ATTCTGCATGTTTAA[A/T]GTAAACTCTCAGGTG | 10600 |
rs190732010 | snp | C/T | 9.8837e-05 | 0.00702914 | missense, utr-variant-5-prime | USP16 | GRCh38.p7 | 21:29034886 | TGAAGCACTATCTGA[C/T]GCCAAGATCTGAACC | 10600 |
rs190778451 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29030932 | TGTATAGGTGGTGGA[A/G]TGTTCTCTGGTACCA | 10600 |
rs190879128 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP16 | GRCh38.p7 | 21:29028539 | CTTGAGGGTTCAAGC[A/G]ATTCTCCTGTCTCAG | 10600 |
rs190989777 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29048134 | TTTCTCCCAGGCTAA[A/G]GTGCAGTGGCCAATT | 10600 |
rs191167941 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | USP16 | GRCh38.p7 | 21:29034076 | GAGGATGTCAGGTTT[C/G]TTTATTAGGAGTTTA | 10600 |
rs191298524 | snp | A/C | | | intron-variant | USP16 | GRCh38.p7 | 21:29030252 | TGACTAAATGAAGGA[A/C]GTTTTCTACAAATCT | 10600 |
rs191398227 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | USP16 | GRCh38.p7 | 21:29039670 | AAGCTAGTTATTAAG[G/T]CCATCATACTTTAAA | 10600 |
rs191499727 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29026287 | ATGGTGAAACCCCGT[C/T]TCTACTAAAAATACA | 10600 |
rs191501922 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP16 | GRCh38.p7 | 21:29035626 | ATCCCCTTGTGATCC[A/G]CATGCCTCAGCCTCC | 10600 |
rs191539156 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | USP16 | GRCh38.p7 | 21:29035305 | GTATGTTATAGATGC[C/T]GCATTGTAACATCAT | 10600 |
rs191726870 | snp | C/G | | | upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29023947 | AATATTTGAAAATCC[C/G]CTCCTCCCCCGCAAT | 10600 |
rs191809274 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | USP16 | GRCh38.p7 | 21:29052499 | TTATTCACTATCAAG[A/C]ATAAGGATGGGAAAG | 10600 |
rs191825184 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29045829 | TTCTTTTTTTTGGGA[A/G]CAGAGTCACTTTGTT | 10600 |
rs191869272 | snp | A/C | 1.68764e-05 | 0.00290481 | missense | USP16 | GRCh38.p7 | 21:29042036 | AAGAAAAAATCAATG[A/C]CAAGTTTTGTTGACC | 10600 |
rs191984247 | snp | C/G | 3.30082e-05 | 0.00406239 | missense, utr-variant-5-prime | USP16 | GRCh38.p7 | 21:29038422 | GAACCACCTGATTTG[C/G]CATTAACAGTATGTT | 10600 |
rs192022168 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29046433 | GATTACAGGTGTGAG[C/G]CGCCATGCCCAGCCA | 10600 |
rs192065030 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | USP16 | GRCh38.p7 | 21:29029152 | GGTGTGGTGGCTCAC[G/T]CCTGTAATCCCAGCA | 10600 |
rs192133835 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29029025 | ACTAATTTCCAGGCC[A/C/T]CCTATTAGCGTAGTA | 10600 |
rs192221103 | snp | A/C | 1.6543e-05 | 0.00287597 | missense | USP16 | GRCh38.p7 | 21:29050128 | GTTAACAAACACATA[A/C]AGTTTCCGGAAATCT | 10600 |
rs192246158 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29032838 | TTTTTTAAGAAACTG[C/T]CAAACTGCCAAACTG | 10600 |
rs192362592 | snp | A/G | 0.0023933 | 0.0345097 | downstream-variant-500B | USP16 | GRCh38.p7 | 21:29054657 | TTGCTCTGTCGCCCA[A/G]GCTGGAGTGCAGTGG | 10600 |
rs192370112 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP16 | GRCh38.p7 | 21:29036015 | AATCTTTTGACTTCA[A/G]TGTTATAACCAGTAA | 10600 |
rs192381699 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP16 | GRCh38.p7 | 21:29029229 | CCATCCTGGCTAACA[C/T]GGTGAAACCCCGTCT | 10600 |
rs192418271 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29053174 | AGGAGACAGTACTAC[C/T]GAAGGGCCGTGATGC | 10600 |
rs192528972 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29049088 | ATGTCCCTCTTTTTA[A/G]TACGATTGGCATCTT | 10600 |
rs192675931 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | USP16 | GRCh38.p7 | 21:29049938 | AGCAAACCAACTTGG[A/G]ATCAGTTAGTGTTCA | 10600 |
rs192740872 | snp | G/T | 1.67919e-05 | 0.00289753 | missense | USP16 | GRCh38.p7 | 21:29046720 | TCATTTAAATGATAT[G/T]TGTACTATTGACCAT | 10600 |
rs192820343 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP16 | GRCh38.p7 | 21:29031766 | TTTTTCACGTTTTCA[A/G]ATTGAAAATCTTATT | 10600 |
rs192873836 | snp | A/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29037212 | TAGTACTGTTTCCCA[A/G]GTATACTTCTGCATT | 10600 |
rs192952202 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | USP16 | GRCh38.p7 | 21:29025775 | TTTATGCCTCAGGTA[C/G]TATTCTATTTTTCTA | 10600 |
rs193177857 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29041313 | AATGGAGAGAATTAC[C/T]CCTGCTGGCATTTTC | 10600 |
rs199586396 | snp | A/G | 0.000313451 | 0.0125151 | missense, utr-variant-5-prime | USP16 | GRCh38.p7 | 21:29037410 | CCTTGCCAAATAACC[A/G]TGAAAGGACTCAGTA | 10600 |
rs199630001 | in-del | -/A | 0.0422008 | 0.138995 | intron-variant | USP16 | GRCh38.p7 | 21:29049120 | CTTTTATTTCAGGTT[-/A]AAAAAAGAAAAAGAC | 10600 |
rs199643978 | snp | A/G | 0.00199806 | 0.0315443 | missense | USP16 | GRCh38.p7 | 21:29046934 | ATGAAAAATATCAAC[A/G]TGGATAATGATCTGG | 10600 |
rs199655977 | snp | G/T | 3.2956e-05 | 0.00405918 | intron-variant | USP16 | GRCh38.p7 | 21:29054053 | TGTTTGATTTTTCAT[G/T]TTCTCATGACAGATT | 10600 |
rs199676270 | snp | C/T | 0.000104179 | 0.00721656 | synonymous-codon | USP16 | GRCh38.p7 | 21:29042014 | TTTTTTCTCCATAGA[C/T]TATGAGAAGAAAAAA | 10600 |
rs199697183 | snp | C/T | 1.64795e-05 | 0.00287045 | synonymous-codon | USP16 | GRCh38.p7 | 21:29053942 | TAATCTTGTTCTTCA[C/T]GGTGATATTCCACAA | 10600 |
rs199847644 | snp | A/G/T | 0.00084214 | 0.0205029 | missense | USP16 | GRCh38.p7 | 21:29042472 | TTCTGATTGGTTAAG[A/G/T]TCTCCTTGGTTCATG | 10600 |
rs199911577 | in-del | -/G | 0.00874735 | 0.0655527 | intron-variant | USP16 | GRCh38.p7 | 21:29044609 | TGTGCCACCGTACCT[-/G]GCTAACTTTTGTATT | 10600 |
rs199977397 | snp | C/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29037508 | AGCTGTCCTTTTCCT[C/T]ATAGAATCTGCTACT | 10600 |
rs200008218 | snp | C/T | | | missense | USP16 | GRCh38.p7 | 21:29047256 | AGAAACTTCGAGATG[C/T]GAATAAACTGCTTTG | 10600 |
rs200021397 | snp | C/G | 0.000446816 | 0.0149402 | missense | USP16 | GRCh38.p7 | 21:29046994 | TTAAATGGTGCCTAC[C/G]TAACGGAAGGGAGCA | 10600 |
rs200075943 | snp | A/C | 0.000399281 | 0.0141238 | missense, utr-variant-5-prime | USP16 | GRCh38.p7 | 21:29036356 | AGAAAACAAGCCAGC[A/C]TTACAACTCCAAAGC | 10600 |
rs200121208 | snp | A/G | 1.66394e-05 | 0.00288434 | utr-variant-3-prime | USP16 | GRCh38.p7 | 21:29054195 | TACTGTAATAATATC[A/G]AAAGCACTTTTTCTG | 10600 |
rs200239859 | in-del | -/AAAC | 0.0119091 | 0.0762411 | intron-variant | USP16 | GRCh38.p7 | 21:29035936 | AAAAACCAAAAAACA[-/AAAC]AAACAAAAAAAAGTT | 10600 |
rs200316224 | snp | G/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29047981 | GTATGTATATATATA[G/T]AAGCTCAGAGACTAT | 10600 |
rs200333544 | snp | C/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29032103 | ATAATCATACCCACC[C/T]CCCTACTGCCACCAC | 10600 |
rs200481781 | snp | C/G/T | 4.96556e-05 | 0.00498254 | intron-variant | USP16 | GRCh38.p7 | 21:29042450 | ATTTACATTTTTACA[C/G/T]TGTCTTTTCTGATTG | 10600 |
rs200527231 | snp | A/G | 5.55592e-05 | 0.00527034 | intron-variant | USP16 | GRCh38.p7 | 21:29047343 | TAATGCTCTCACTGT[A/G]AGTAAAATTAATATT | 10600 |
rs200606379 | snp | A/G | 0.000148288 | 0.00860943 | missense | USP16 | GRCh38.p7 | 21:29054101 | GGGCAGTGGTTTCAC[A/G]TCAGCGACACACATG | 10600 |
rs200609671 | snp | A/G | 3.43702e-05 | 0.00414535 | intron-variant | USP16 | GRCh38.p7 | 21:29027977 | TCTGAAACTTTAGGT[A/G]TATTTCATTGATTGA | 10600 |
rs200770677 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29042131 | TCATGTATACTGGGT[A/T]TATTTGCTAATATTC | 10600 |
rs200819693 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29048889 | AATTTGTTTTAAATA[C/T]GTAACACCTACTTTA | 10600 |
rs200853477 | snp | C/T | 0.00199802 | 0.0315439 | missense | USP16 | GRCh38.p7 | 21:29046766 | TATGAAGCTGAAATG[C/T]CACTTCAAGGAGAAG | 10600 |
rs200880917 | snp | G/T | 6.83691e-05 | 0.00584635 | stop-gained, utr-variant-5-prime | USP16 | GRCh38.p7 | 21:29027974 | TCCTCTGAAACTTTA[G/T]GTATATTTCATTGAT | 10600 |
rs200929235 | in-del | -/T | 0.00158148 | 0.0280756 | intron-variant | USP16 | GRCh38.p7 | 21:29038310 | TAAATAATTTTTCTC[-/T]TTTTTTTTTCACCCT | 10600 |
rs200981777 | snp | C/T | 0.000153988 | 0.00877327 | stop-gained | USP16 | GRCh38.p7 | 21:29046673 | TTTACCCAGAACCAA[C/T]GAAGACAACAAAAAA | 10600 |
rs201047792 | snp | G/T | 3.29538e-05 | 0.00405904 | missense, utr-variant-5-prime | USP16 | GRCh38.p7 | 21:29034940 | ACAACTGGAGTGTAT[G/T]GTGAGTTTCAGTTCC | 10600 |
rs201082088 | snp | A/C/T | 8.46059e-05 | 0.00650352 | missense | USP16 | GRCh38.p7 | 21:29042085 | TAACTAGTATGATCA[A/C/T]GTGTGATCAATGCAG | 10600 |
rs201366690 | in-del | -/T | | | intron-variant, upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29026853 | TTATAACTTTAGTGG[-/T]TTTTTTTTGTTGTTG | 10600 |
rs201426689 | snp | A/G | 0.000399281 | 0.0141238 | synonymous-codon | USP16 | GRCh38.p7 | 21:29046996 | AAATGGTGCCTACCT[A/G]ACGGAAGGGAGCAAT | 10600 |
rs201568491 | snp | C/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29034302 | TGAGTGCATGGTTTT[C/T]TTTTTTTTTTTTTTT | 10600 |
rs201576855 | in-del | -/T | 0.0111196 | 0.0737302 | intron-variant | USP16 | GRCh38.p7 | 21:29044342 | AATATGCAGTCTTGG[-/T]TTTTTTCCCCCTTTC | 10600 |
rs201674842 | snp | A/G | 0.000360153 | 0.0134144 | missense | USP16 | GRCh38.p7 | 21:29042099 | ATGTGTGATCAATGC[A/G]GAACTGTAAGTAGAT | 10600 |
rs201747359 | in-del | -/G | | | frameshift-variant | USP16 | GRCh38.p7 | 21:29047053 | CAAAAACCTAAATTT[-/G]AATGCTGCTCTTCAT | 10600 |
rs201803145 | snp | G/T | 0.00199799 | 0.0315437 | stop-lost | USP16 | GRCh38.p7 | 21:29054185 | TATGAGAGAATACTG[G/T]AATAATATCAAAAGC | 10600 |
rs201875942 | snp | A/C/T | 3.45998e-05 | 0.0041592 | synonymous-codon | USP16 | GRCh38.p7 | 21:29040626 | AGTGAGTAAAGGAAT[A/C/T]CTTAAAGCATTTGGT | 10600 |
rs201909001 | snp | A/T | 1.69015e-05 | 0.00290696 | intron-variant | USP16 | GRCh38.p7 | 21:29053787 | CTAACTTTTGGATTC[A/T]ACTCATTTTTAAAGA | 10600 |
rs201922742 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29043604 | AGCAAGCCAAGGTGG[G/T]TAATTAGGAGGAAAA | 10600 |
rs367734433 | snp | G/T | 1.91188e-05 | 0.00309177 | intron-variant | USP16 | GRCh38.p7 | 21:29037507 | AAGCTGTCCTTTTCC[G/T]CATAGAATCTGCTAC | 10600 |
rs367885524 | snp | A/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29044298 | ACGTATCCTTCTGGA[A/G]TTTCTTTTGGAAAAT | 10600 |
rs368083075 | snp | A/G | | | upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29023211 | CAGTGAGCTGAGGTC[A/G]TGCCACTGCACTCCA | 10600 |
rs368224663 | in-del | -/TTCT | | | upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29022619 | CAGGGGGAAGAGGCT[-/TTCT]GACAGGAAGCACGTG | 10600 |
rs368279455 | snp | C/G | 0.000153988 | 0.00877328 | missense, utr-variant-5-prime | USP16 | GRCh38.p7 | 21:29037302 | AATGGAAATATTGAA[C/G]TTGAAAATAAAAAAT | 10600 |
rs368342387 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | USP16 | GRCh38.p7 | 21:29033836 | ACAGTATTTTCTCAT[C/T]TGGGAGATAAGTATA | 10600 |
rs368372769 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | USP16 | GRCh38.p7 | 21:29042123 | AGTAGATGTCATGTA[C/T]ACTGGGTTTATTTGC | 10600 |
rs368406859 | snp | A/G | 0.000334747 | 0.012933 | intron-variant | USP16 | GRCh38.p7 | 21:29039205 | TCAGTGAGATGCTGA[A/G]AAATAATATTAATAT | 10600 |
rs368459557 | snp | C/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29052364 | ACATGGCTGGGGAGG[C/T]CTCACAGTCATGGCG | 10600 |
rs368523988 | snp | A/G | 1.66852e-05 | 0.0028883 | missense | USP16 | GRCh38.p7 | 21:29043489 | GAAGATCAAGATAGT[A/G]AGGAAGAAAAAGATA | 10600 |
rs368525941 | snp | C/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29034685 | ATATGTAAGTTTTAA[C/T]AAAATATTGATTCTA | 10600 |
rs368743480 | snp | C/G | | | missense | USP16 | GRCh38.p7 | 21:29053944 | ATCTTGTTCTTCACG[C/G]TGATATTCCACAAGG | 10600 |
rs368763898 | snp | A/C | 4.96438e-05 | 0.00498191 | missense | USP16 | GRCh38.p7 | 21:29046959 | ATCTGGAGGTTTTAA[A/C]ATCTTCTCCCACTAG | 10600 |
rs368837459 | snp | A/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29048176 | CAATCTCCACCTCCC[A/G]GGTTCAAGAGATTCT | 10600 |
rs368873441 | snp | C/T | 1.64838e-05 | 0.00287083 | missense | USP16 | GRCh38.p7 | 21:29047187 | CAAACAGGGAAGTTT[C/T]CAATACTGATGAGTG | 10600 |
rs368950103 | snp | C/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29031113 | TGGATGTGGCCTGCC[C/T]CTAGAGCAGGAAGTA | 10600 |
rs369104411 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29031933 | ACACCAATCGCAATC[A/G]GATCTCCTGAGTTTG | 10600 |
rs369105286 | snp | C/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29045953 | TGGGATTACAGGCGC[C/G]CACCACCCATGTGTG | 10600 |
rs369230878 | snp | A/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29031593 | CAGGTGTGTGCCACC[A/G]CGCCTGGCTGAGTTT | 10600 |
rs369464271 | snp | A/T | 0.000197883 | 0.00994496 | missense, utr-variant-5-prime | USP16 | GRCh38.p7 | 21:29039089 | ATGAGCCAGTTTCTT[A/T]ATGAGATGCAAGAGA | 10600 |
rs369470289 | snp | A/C | | | intron-variant | USP16 | GRCh38.p7 | 21:29033090 | TAAATACATATGGTG[A/C]GTATGAATATGCTTT | 10600 |
rs369617141 | snp | A/G | 0.000181646 | 0.00952837 | missense | USP16 | GRCh38.p7 | 21:29046820 | TCACAAGAGGGTGTT[A/G]TGCATAAAGAATATT | 10600 |
rs369634800 | in-del | -/TAAG | | | intron-variant | USP16 | GRCh38.p7 | 21:29037921 | TTTATTGCATGACAG[-/TAAG]AGAGTTTGGTGAGCA | 10600 |
rs369751616 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29024793 | GTGAGTTCTGGTCCC[A/G]CTGCCTGGCAGTCGT | 10600 |
rs369754224 | snp | A/G | 0.000153988 | 0.00877328 | utr-variant-5-prime, upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29027908 | AGTAATCCATAAAGT[A/G]CCAACATGGGAAAGA | 10600 |
rs369773911 | snp | C/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29052299 | ATATACTGGACAAGA[C/T]ATACTGGGCAAGACT | 10600 |
rs369995597 | snp | G/T | | | upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29023121 | TACAAAAGTTAGCTG[G/T]GTGGTGGGGTGGCAC | 10600 |
rs370073470 | snp | G/T | | | intron-variant, upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29026506 | GCAGGTAAAAAGTGG[G/T]GGTCTTGAAACCCAA | 10600 |
rs370151884 | snp | C/T | 7.04089e-05 | 0.00593292 | intron-variant | USP16 | GRCh38.p7 | 21:29030819 | TTTTAGAAAACTCTT[C/T]GAACTTACTTTAGAA | 10600 |
rs370221591 | snp | A/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29048481 | ATTGTGTCTCTCCAC[A/G]GTAATTCAATTTTGC | 10600 |
rs370296808 | snp | C/T | 0.000329435 | 0.01283 | missense | USP16 | GRCh38.p7 | 21:29053875 | GTGGTACTATGAGGT[C/T]GGGGCATTACACTGC | 10600 |
rs370303209 | snp | A/G | 0.000236415 | 0.0108697 | intron-variant | USP16 | GRCh38.p7 | 21:29050187 | ATGTAAGGTAAGTCA[A/G]AGTGGTCTTTTTCAG | 10600 |
rs370331604 | snp | A/T | 0.000437904 | 0.0147905 | intron-variant | USP16 | GRCh38.p7 | 21:29039428 | TTTTCTAAAAATAGC[A/T]TCAGAGCTTAGTAGA | 10600 |
rs370393349 | snp | A/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29033479 | GTTGTACTGTGATCC[A/G]AAAGTTGATAGACTG | 10600 |
rs370468199 | snp | C/G | 3.34554e-05 | 0.00408982 | intron-variant | USP16 | GRCh38.p7 | 21:29039475 | TGTCTTTTTGTTTTT[C/G]TCTAGAGCAGTGCGG | 10600 |
rs370504916 | snp | A/G | | | missense | USP16 | GRCh38.p7 | 21:29047207 | ACTGATGAGTGTTCA[A/G]TCCAACATTGTTTAT | 10600 |
rs370609898 | snp | C/G | 0.000562737 | 0.0167646 | intron-variant | USP16 | GRCh38.p7 | 21:29042448 | GTATTTACATTTTTA[C/G]ACTGTCTTTTCTGAT | 10600 |
rs370881892 | snp | C/G/T | 0.000169986 | 0.00921759 | intron-variant | USP16 | GRCh38.p7 | 21:29046623 | TCCTTTTCTCCCGCT[C/G/T]TTTCTTTTTCTTTAT | 10600 |
rs370930670 | snp | C/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29028051 | AAAAATGGTATAAAG[C/G]TGCATATTATTGTTA | 10600 |
rs370943105 | snp | A/T | 3.33778e-05 | 0.00408507 | intron-variant | USP16 | GRCh38.p7 | 21:29048754 | AAAAATTTCTTCTTT[A/T]CTTTAGGTGAAAGGA | 10600 |
rs371056613 | snp | C/G | 1.6748e-05 | 0.00289374 | missense, utr-variant-5-prime | USP16 | GRCh38.p7 | 21:29037328 | AAAATTAGAAAAAGA[C/G]AGTAAGAATGAACAA | 10600 |
rs371115282 | snp | G/T | 1.64977e-05 | 0.00287203 | missense, utr-variant-5-prime | USP16 | GRCh38.p7 | 21:29036354 | TCAGAAAACAAGCCA[G/T]CATTACAACTCCAAA | 10600 |
rs371147314 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | USP16 | GRCh38.p7 | 21:29041991 | GGTAATTGGTAATTG[A/G]TAGACTTTTTTTTCT | 10600 |
rs371253238 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP16 | GRCh38.p7 | 21:29041387 | GCTTATAGGTTTCAC[A/G]TATTTGGAAAATTGG | 10600 |
rs371331684 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29027458 | TATCAGTTTAATTTG[C/T]ATAGACTGCAGAGCT | 10600 |
rs371371933 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29026963 | GTGTGGTCCAGGAAA[C/T]TGTTAAATGCTTCCG | 10600 |
rs371404692 | snp | A/G | 1.65179e-05 | 0.00287379 | synonymous-codon | USP16 | GRCh38.p7 | 21:29042528 | AGTTTTAGATGATCA[A/G]GTAAGACTATTGAAT | 10600 |
rs371771429 | snp | A/T | 0.000953948 | 0.0218189 | intron-variant | USP16 | GRCh38.p7 | 21:29037232 | ACTTCTGCATTCGAT[A/T]TGACTGTATTACACA | 10600 |
rs371776163 | snp | A/G/T | 1.7894e-05 | 0.0029911 | missense | USP16 | GRCh38.p7 | 21:29043438 | AGTGGTAAGAAAAGT[A/G/T]TAAATGATAAAAATC | 10600 |
rs371791316 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29035154 | CATAGAAGACTTAAG[A/C]ATCTTTACCCCTTTG | 10600 |
rs371849624 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29051650 | AGCCTGGCCAGCATG[A/G]TGAAACCCTGTCTCT | 10600 |
rs371959141 | snp | A/C | | | intron-variant | USP16 | GRCh38.p7 | 21:29044334 | CAAATACAAATATGC[A/C]GTCTTGGTTTTTTTC | 10600 |
rs371975191 | snp | C/G | | | upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29024261 | AACAAAAAATCACTC[C/G]CTGCGTTTTTTATTC | 10600 |
rs372025248 | snp | G/T | 3.29679e-05 | 0.00405991 | synonymous-codon | USP16 | GRCh38.p7 | 21:29054130 | TGTGCAAGCTGTGCC[G/T]ACAACTAAAGTACTA | 10600 |
rs372092817 | snp | A/C | 0.001493 | 0.0272813 | intron-variant | USP16 | GRCh38.p7 | 21:29037505 | AAAAGCTGTCCTTTT[A/C]CTCATAGAATCTGCT | 10600 |
rs372200254 | snp | C/T | 0.000153988 | 0.00877328 | synonymous-codon, utr-variant-5-prime | USP16 | GRCh38.p7 | 21:29038406 | AACAATTGTAAAAAT[C/T]GAACCACCTGATTTG | 10600 |
rs372361644 | snp | A/G | 5.26764e-05 | 0.00513181 | intron-variant | USP16 | GRCh38.p7 | 21:29043613 | AGGTGGGTAATTAGG[A/G]GGAAAATCATATGCT | 10600 |
rs372405346 | snp | A/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29052388 | CATGGCGGAAGGCAA[A/G]GAGGAGCACGTCACA | 10600 |
rs372478500 | snp | C/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29045980 | TGTGCATTACAGGCA[C/T]GCCTGGCTAATTTTT | 10600 |
rs372502740 | snp | A/C | 1.64939e-05 | 0.0028717 | synonymous-codon | USP16 | GRCh38.p7 | 21:29047206 | TACTGATGAGTGTTC[A/C]ATCCAACATTGTTTA | 10600 |
rs372527465 | in-del | -/AC | | | intron-variant | USP16 | GRCh38.p7 | 21:29028122 | ATTTAATAGTCTTCT[-/AC]TTTTTTTTTTTTTTT | 10600 |
rs372831501 | snp | A/G | 0.000296604 | 0.0121743 | intron-variant | USP16 | GRCh38.p7 | 21:29054007 | GATTACGGCAAAACC[A/G]AAAAGTAATCAACTT | 10600 |
rs372868485 | snp | C/T | 7.59561e-05 | 0.00616217 | intron-variant | USP16 | GRCh38.p7 | 21:29046649 | TTTATTTTTTGATGC[C/T]GTATACTTTTTACCC | 10600 |
rs372869578 | snp | C/T | 0.00046463 | 0.0152348 | intron-variant | USP16 | GRCh38.p7 | 21:29039171 | AGTGAGTATCCACTT[C/T]GATTGTGCTTTCAGT | 10600 |
rs372904983 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP16 | GRCh38.p7 | 21:29030301 | ATAAGTATGATAAAG[A/G]GCCTTAATTTAAAGG | 10600 |
rs373025538 | snp | A/T | 1.71287e-05 | 0.00292644 | intron-variant | USP16 | GRCh38.p7 | 21:29048895 | TTTTAAATATGTAAC[A/T]CCTACTTTATTACCT | 10600 |
rs373038005 | snp | C/T | 0.000153988 | 0.00877327 | intron-variant | USP16 | GRCh38.p7 | 21:29047355 | TGTAAGTAAAATTAA[C/T]ATTCAGGGGCACATT | 10600 |
rs373106142 | snp | C/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29037053 | TTTGGTTTCATTTAT[C/G]AAACTAATGCTTACT | 10600 |
rs373130630 | snp | C/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29036218 | ATTATTATTTGTCTC[C/T]CCCTTTTTAGTTGTC | 10600 |
rs373131505 | snp | G/T | | | intron-variant, upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29027599 | CTGTTCAAGATCTGT[G/T]TAAGATGACCAAGGT | 10600 |
rs373279774 | snp | A/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29053197 | CGTGATGCCTGTTAC[A/G]GACTTTTACATGAGA | 10600 |
rs373351842 | snp | A/C/G | 0.0002146 | 0.0103568 | missense | USP16 | GRCh38.p7 | 21:29046862 | AAAGATTTGAATGGC[A/C/G]AAGCAAAAATGATCG | 10600 |
rs373372631 | snp | A/T | 2.2158e-05 | 0.00332844 | intron-variant | USP16 | GRCh38.p7 | 21:29043396 | TTGTAAAATTTTGTT[A/T]TTGACCTATGTTATC | 10600 |
rs373447233 | snp | G/T | 1.66801e-05 | 0.00288787 | missense, upstream-variant-2KB, utr-variant-5-prime | USP16 | GRCh38.p7 | 21:29027936 | AGAAACGGACAAAGG[G/T]AAAAACTGTTCCAAT | 10600 |
rs373497111 | snp | A/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29045122 | TTTTTATGTTTCAGA[A/G]CCATTTGCATTTCAT | 10600 |
rs373549237 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29033123 | TATTTCAGTTTTTCA[C/G]AATATATTTTGTGTT | 10600 |
rs373623849 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29049537 | TGGCTGAAGCAGAAA[C/T]ATTGAGAATTTTCTC | 10600 |
rs373724993 | snp | A/C | 1.64917e-05 | 0.00287151 | missense, utr-variant-5-prime | USP16 | GRCh38.p7 | 21:29039104 | AATGAGATGCAAGAG[A/C]CCAAAAAGGGGGTTG | 10600 |
rs373736290 | in-del | -/A | | | upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29024347 | GACAGGACAGAATTA[-/A]CGGAAACAAATTTAA | 10600 |
rs373804711 | snp | A/T | 0.000250081 | 0.0111794 | intron-variant | USP16 | GRCh38.p7 | 21:29039020 | AATTTCTTTTCCCAT[A/T]TTCAGGAACCATTAG | 10600 |
rs373891812 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29026936 | AAGGCCTATGAGTGC[A/G]AAGTTTAGGGAGTGT | 10600 |
rs373939904 | snp | A/G | 1.6549e-05 | 0.0028765 | synonymous-codon, utr-variant-5-prime | USP16 | GRCh38.p7 | 21:29037352 | TGAACAAGAGAGAGA[A/G]AAGAAGGAAAACATG | 10600 |
rs373949018 | snp | C/T | 1.65217e-05 | 0.00287412 | synonymous-codon | USP16 | GRCh38.p7 | 21:29048786 | GCATGTTTACACCAA[C/T]GCCAAAAAGCAGATG | 10600 |
rs373992561 | snp | A/G | 7.5503e-05 | 0.00614376 | intron-variant | USP16 | GRCh38.p7 | 21:29046650 | TTATTTTTTGATGCC[A/G]TATACTTTTTACCCA | 10600 |
rs374016640 | in-del | -/T | 0.0520825 | 0.152737 | intron-variant, upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29026724 | TGTGATCTTTCACCA[-/T]TTTTTTTTCCTGACT | 10600 |
rs374030820 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | USP16 | GRCh38.p7 | 21:29050202 | AAGTGGTCTTTTTCA[A/G]GAAAGTCCTTTAAAG | 10600 |
rs374153931 | snp | C/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29029646 | TTACTTATCTTGGCC[C/T]CAACAGAGTTTTCAG | 10600 |
rs374207669 | snp | A/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29047449 | TTTTCTGTGTAAATA[A/T]TTTAATAGGATGGAA | 10600 |
rs374389635 | snp | C/T | 1.68408e-05 | 0.00290175 | intron-variant | USP16 | GRCh38.p7 | 21:29039585 | TTAGCATGTTATGAC[C/T]ATTGTATTTTATGAT | 10600 |
rs374675365 | snp | C/G | 0.000155988 | 0.00883004 | intron-variant | USP16 | GRCh38.p7 | 21:29037253 | GTATTACACATTTTG[C/G]TAAATCTTTTCTTTT | 10600 |
rs374793415 | in-del | -/A | | | intron-variant | USP16 | GRCh38.p7 | 21:29033032 | TCTGTATGTTAGAAA[-/A]GATACTGTTTACTTG | 10600 |
rs374957629 | snp | A/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29029059 | TGCCCATTTCCCTGA[A/G]CCTTCATCGGCACTG | 10600 |
rs375052643 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP16 | GRCh38.p7 | 21:29043753 | ATTTAGTATTCTCTG[C/T]AGGGAAATTGCTTTG | 10600 |
rs375073301 | snp | A/G | 3.34325e-05 | 0.00408842 | intron-variant | USP16 | GRCh38.p7 | 21:29039192 | TGCTTTCAGTGCCTC[A/G]GTGAGATGCTGAGAA | 10600 |
rs375076156 | snp | C/T | 3.81832e-05 | 0.00436923 | intron-variant | USP16 | GRCh38.p7 | 21:29041998 | GGTAATTGATAGACT[C/T]TTTTTTCTCCATAGA | 10600 |
rs375089661 | snp | C/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29052776 | TTTATGTCCCTTCAG[C/T]TCAGGAGTTTGAGAC | 10600 |
rs375209353 | snp | C/G | | | upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29024094 | AGGAGTTGGAGACCA[C/G]CCTGGCCAATTGGTG | 10600 |
rs375218341 | snp | G/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29036952 | CTTGATTGTTTTATA[G/T]TCTTAATTTCACAAG | 10600 |
rs375477618 | snp | C/G | 3.29587e-05 | 0.00405934 | intron-variant | USP16 | GRCh38.p7 | 21:29054043 | TTTCCATTTATGTTT[C/G]ATTTTTCATTTTCTC | 10600 |
rs375480955 | snp | C/T | 0.000346018 | 0.0131487 | intron-variant | USP16 | GRCh38.p7 | 21:29053968 | CACAAGGTAAGATGT[C/T]TTGGAAAATTCAGGC | 10600 |
rs375561676 | snp | G/T | 0.000153988 | 0.00877328 | missense, utr-variant-5-prime | USP16 | GRCh38.p7 | 21:29038416 | AAAATTGAACCACCT[G/T]ATTTGGCATTAACAG | 10600 |
rs375586235 | snp | C/G/T | 4.9516e-05 | 0.00497549 | missense, utr-variant-5-prime | USP16 | GRCh38.p7 | 21:29039126 | AGGGGGTTGTGACAC[C/G/T]GAAAGAACTCTTTTC | 10600 |
rs375716738 | snp | C/T | 5.5179e-05 | 0.00525228 | intron-variant | USP16 | GRCh38.p7 | 21:29037496 | TCCCTTTAAAAAAGC[C/T]GTCCTTTTCCTCATA | 10600 |
rs375967069 | snp | C/G | | | upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29023465 | TACATATCTATTTTT[C/G]TATAGCTATCTGCAA | 10600 |
rs376051518 | in-del | -/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29037574 | TTCTATGTATCCAAA[-/G]AAAACTTTTTTTTTT | 10600 |
rs376063644 | snp | A/G | 1.65176e-05 | 0.00287376 | missense | USP16 | GRCh38.p7 | 21:29048791 | TTTACACCAATGCCA[A/G]AAAGCAGATGCTAAT | 10600 |
rs376127428 | snp | A/T | 1.6681e-05 | 0.00288794 | synonymous-codon, upstream-variant-2KB, utr-variant-5-prime | USP16 | GRCh38.p7 | 21:29027937 | GAAACGGACAAAGGG[A/T]AAAACTGTTCCAATC | 10600 |
rs376248736 | snp | C/T | 0.000129592 | 0.00804857 | intron-variant | USP16 | GRCh38.p7 | 21:29043402 | AATTTTGTTTTTGAC[C/T]TATGTTATCTATATT | 10600 |
rs376263224 | snp | C/T | 1.67033e-05 | 0.00288987 | intron-variant | USP16 | GRCh38.p7 | 21:29050089 | GTTATGCTTCTCTTT[C/T]AGGCTGGTTTTAACC | 10600 |
rs376300038 | snp | G/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29034673 | AGTTGCCTGTGCATA[G/T]GTAAGTTTTAACAAA | 10600 |
rs376301370 | snp | C/T | 0.000100012 | 0.00707077 | synonymous-codon | USP16 | GRCh38.p7 | 21:29046735 | TTGTACTATTGACCA[C/T]CCTGAAGACAGTGAA | 10600 |
rs376320329 | snp | A/G | 6.61113e-05 | 0.00574903 | missense, utr-variant-5-prime | USP16 | GRCh38.p7 | 21:29036362 | CAAGCCAGCATTACA[A/G]CTCCAAAGCCAGGTA | 10600 |
rs376368961 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP16 | GRCh38.p7 | 21:29053660 | CTGAGAAGAGGTATG[A/G]AGAAAAGAGTAGACT | 10600 |
rs376420320 | snp | C/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29033255 | ATTCTTAACTGTTGT[C/G]TCAAGACAACTATGT | 10600 |
rs376430261 | snp | G/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29053489 | GTTAATAGCTAGGGT[G/T]GTTAAGAATTATCCT | 10600 |
rs376851609 | snp | C/T | | | upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29024441 | AGGCTCAGACCACCA[C/T]CGGATGCCCACACTT | 10600 |
rs376971834 | snp | A/T | 0.000153988 | 0.00877328 | intron-variant | USP16 | GRCh38.p7 | 21:29050214 | TCAGGAAAGTCCTTT[A/T]AAGTCAAATTGTGGC | 10600 |
rs377180033 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP16 | GRCh38.p7 | 21:29044345 | TGAGAAAGGGGGAAA[A/G]AAACCAAGACTGCAT | 10600 |
rs377219525 | snp | A/G | 0.000342126 | 0.0130746 | intron-variant | USP16 | GRCh38.p7 | 21:29030791 | ATGCTTACGTTTTAA[A/G]ATCAATATGGGATTT | 10600 |
rs377265091 | snp | C/T | 6.0614e-05 | 0.00550485 | intron-variant | USP16 | GRCh38.p7 | 21:29046619 | TTCCTCCTTTTCTCC[C/T]GCTCTTTCTTTTTCT | 10600 |
rs377322556 | snp | C/T | 0.0001 | 0.00707036 | missense | USP16 | GRCh38.p7 | 21:29047285 | TGTGAAGTATGCACA[C/T]GGAGACAGTGTAATG | 10600 |
rs377329858 | snp | A/T | 1.68451e-05 | 0.00290211 | intron-variant | USP16 | GRCh38.p7 | 21:29039470 | TTTTCTGTCTTTTTG[A/T]TTTTCTCTAGAGCAG | 10600 |
rs377344532 | in-del | -/AGT | | | intron-variant | USP16 | GRCh38.p7 | 21:29043379 | TTTTCACCAAATGGT[-/AGT]TGTAAAATTTTGTTT | 10600 |
rs377459112 | snp | C/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29038128 | GGTGGGAGAATGCCC[C/T]ACTGAGGTGATGAAT | 10600 |
rs377539518 | snp | C/T | 1.65836e-05 | 0.0028795 | intron-variant | USP16 | GRCh38.p7 | 21:29038461 | TTTTCTAGTCTGTAA[C/T]TTTCCTCTCTGAATG | 10600 |
rs377670056 | snp | A/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29047764 | TGACAATTTCCCTTA[A/T]CTCCCCATTGCTTTT | 10600 |
rs386817760 | multinucleotide-polymorphism | CA/TG | | | intron-variant | USP16 | GRCh38.p7 | 21:29031555 | GCAGTTTTCCTGCCT[CA/TG]GTCTCCAAGTAGCTG | 10600 |
rs397817668 | in-del | -/T/TG/TTG | 0 | 0 | intron-variant | USP16 | GRCh38.p7 | 21:29028139 | TTTTTTTTTTTTTTT[-/T/TG/TTG]GAGAAAGAATCTCGC | 10600 |
rs398101579 | in-del | -/A | | | intron-variant | USP16 | GRCh38.p7 | 21:29037493 | TTTCCCTTTAAAAAA[-/A]GCTGTCCTTTTCCTC | 10600 |
rs527424809 | snp | C/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29032606 | AGTTTGCTCTTTTTT[C/T]ATTACTGAGCGTATT | 10600 |
rs527562811 | snp | C/T | 0 | 0 | synonymous-codon | USP16 | GRCh38.p7 | 21:29042065 | CCGCATCTTTGGTGG[C/T]GAACTAACTAGTATG | 10600 |
rs527617742 | snp | C/T | 0.000399281 | 0.0141238 | synonymous-codon | USP16 | GRCh38.p7 | 21:29048789 | TGTTTACACCAATGC[C/T]AAAAAGCAGATGCTA | 10600 |
rs527625227 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | USP16 | GRCh38.p7 | 21:29041331 | TGCTGGCATTTTCTG[A/T]CAGAAAAGTGTGGTT | 10600 |
rs527640450 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29035003 | TAGAGAATGGAAATG[A/T]TTAAATATGTTTAAG | 10600 |
rs527641720 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29027812 | GTTATATTACTGTCT[C/T]CTAGAGAAATATAAG | 10600 |
rs527657718 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | USP16 | GRCh38.p7 | 21:29052466 | TCCCCCTTAAGAAAC[C/G]ATCAGCTCTCATGAG | 10600 |
rs527701065 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29034495 | TTTTTGTATTTTTAG[C/T]AGAGATGGGGTTTCA | 10600 |
rs527777857 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP16 | GRCh38.p7 | 21:29028366 | TCCTGGCCTCAAGTG[A/G]TCCGCCTGCCTTGGC | 10600 |
rs527851148 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP16 | GRCh38.p7 | 21:29028724 | ACAGGCGTGAGCCAC[C/T]GCGCCCGACCTTCAA | 10600 |
rs528113378 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP16 | GRCh38.p7 | 21:29050589 | ATTTAAAGAAGGAGT[A/G]AAAGTATGATGAATC | 10600 |
rs528285380 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29036620 | AGACTAAGGTAATTC[C/G]CATAACCCTAGCCAG | 10600 |
rs528365992 | snp | C/G | | | upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29023517 | CGATTACTATCTTCT[C/G]TACTAAACTAAGACT | 10600 |
rs528533119 | in-del | -/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29045564 | TTTTCTTTCAGTTTG[-/T]TTTTTTTTTTTCTCT | 10600 |
rs528547258 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29052152 | TCTAGTATGGGATCA[A/T]AAATTCTGCATGTTT | 10600 |
rs528619798 | snp | C/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29049350 | TCAGTATCTTCAGAA[C/T]GTTTTGCCTCTTGTG | 10600 |
rs528709528 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29045065 | ATTATCTCAGTGCAG[A/T]TTTATTTTACATTTA | 10600 |
rs528819292 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | USP16 | GRCh38.p7 | 21:29045564 | GTTTTCTTTCAGTTT[G/T]TTTTTTTTTTTCTCT | 10600 |
rs528878289 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29049044 | TGAAGATGGAGGCAC[A/G]ATCTCCTCAGATTTC | 10600 |
rs528923355 | in-del | -/T | 0.00199481 | 0.0315187 | intron-variant | USP16 | GRCh38.p7 | 21:29039214 | TGCTGAGAAATAATA[-/T]TAATATTAAATAGTA | 10600 |
rs529033779 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29028529 | CAGCCTTTGCCTTGA[C/G]GGTTCAAGCGATTCT | 10600 |
rs529183909 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29029094 | GTATCATCTGTAAAC[A/C]TCTGTGCTGATTTGG | 10600 |
rs529510640 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | USP16 | GRCh38.p7 | 21:29051557 | AATTTGGGGCTGGGC[A/G]TGGTGGCTTACGCCT | 10600 |
rs529607902 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29044997 | GCTCCTGACCCTTGA[C/T]AGCTGTGTGTTATCA | 10600 |
rs529670303 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP16 | GRCh38.p7 | 21:29038258 | TTTTCTGTTTTGATA[A/G]AATAGACACTTAAGA | 10600 |
rs529745029 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29031525 | CTCATGGCAGCCTCC[A/G]CCTCCCAGGTTCAAG | 10600 |
rs529786541 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29023309 | TCAGCAGTAAAAAGC[A/T]AGAGAGCTAGTTTTC | 10600 |
rs529798880 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | USP16 | GRCh38.p7 | 21:29044062 | CTCAGCCTCCTGAGC[A/C]GTCAGGACTACAGGT | 10600 |
rs529855164 | snp | A/G | | | utr-variant-5-prime, upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29024722 | GAGGAAGACGGAGCT[A/G]GCTGCCCAGCCCAAA | 10600 |
rs529876443 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29024380 | GTTCCCCCTTTTAGC[C/T]CCAAATATAATGTGT | 10600 |
rs530061576 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29053527 | CTAAAGAAACTGGCA[A/G]GTTGAATTCAGTTAT | 10600 |
rs530112880 | snp | A/G | 8.29855e-05 | 0.00644095 | intron-variant | USP16 | GRCh38.p7 | 21:29039172 | GTGAGTATCCACTTC[A/G]ATTGTGCTTTCAGTG | 10600 |
rs530167109 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29046468 | CGTCATAATTTTTTT[G/T]ATCCTTGATAGCAAA | 10600 |
rs530247465 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29040139 | TAATTCCCTTACTTC[A/G]TTCTCACAAAGTTTC | 10600 |
rs530321113 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29025800 | TTTCTATTTCAATGC[A/G]AGAAGTATTTCTTCA | 10600 |
rs530475959 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | USP16 | GRCh38.p7 | 21:29050853 | GTTTAAAGCACTGGG[G/T]TGGCATGGTCAGATC | 10600 |
rs530518753 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29029700 | TGCACATTGTGTAAC[G/T]CCATCATCTGGGGAG | 10600 |
rs530519631 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29037635 | TCTGTCACTCGGCTG[C/G]AGTGCAGTGGCACGA | 10600 |
rs530530015 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29044236 | ACCGCGCCCGGCCGA[C/T]CACCACTTTCCTTTT | 10600 |
rs530604507 | in-del | -/GT | 0.491051 | 0.0662916 | intron-variant | USP16 | GRCh38.p7 | 21:29048049 | GCTCAGAGACGATAC[-/GT]GTGTGTGTGTGTGTG | 10600 |
rs530652608 | snp | A/G | 0.000221211 | 0.0105146 | intron-variant | USP16 | GRCh38.p7 | 21:29030784 | ATCAGGTATGCTTAC[A/G]TTTTAAGATCAATAT | 10600 |
rs530794486 | in-del | -/TT | 0.497776 | 0.0332724 | intron-variant | USP16 | GRCh38.p7 | 21:29037580 | GTATCCAAAGAAAAC[-/TT]TTTTTTTTTTTTTTT | 10600 |
rs530924979 | snp | A/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29051518 | GGACACCACAAAGGA[A/T]CTCAAAGAATCTCCA | 10600 |
rs530971875 | snp | A/C/G | 3.29958e-05 | 0.00406165 | synonymous-codon, utr-variant-5-prime | USP16 | GRCh38.p7 | 21:29039115 | AGAGACCAAAAAGGG[A/C/G]GTTGTGACACCGAAA | 10600 |
rs531012858 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP16 | GRCh38.p7 | 21:29046379 | ACTCCTCAAGTGATC[C/G]TCTTGTGATCATCTT | 10600 |
rs531092868 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29031719 | GCTAGGAATACAGGC[A/G]TGAGCCACTGCGCCC | 10600 |
rs531108133 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29032123 | ACTGCCACCACTCTC[C/T]GCAGCCCCTGGCAAC | 10600 |
rs531306635 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29025624 | GAGTCTAAGCTGCTG[C/T]AATCCTCAAACCAGA | 10600 |
rs531563810 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP16 | GRCh38.p7 | 21:29033870 | TTCTGGGAGGAGGTG[A/G]CTTTTGAGCAAGATC | 10600 |
rs531628160 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29041312 | TAATGGAGAGAATTA[A/C]CCCTGCTGGCATTTT | 10600 |
rs531629614 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29047921 | AGCCTGTGTGTGTGT[G/T]TATGTATCTTATATG | 10600 |
rs531689980 | in-del | -/CTA | 0.000798403 | 0.0199641 | intron-variant | USP16 | GRCh38.p7 | 21:29028120 | TCATTTAATAGTCTT[-/CTA]CTTTTTTTTTTTTTT | 10600 |
rs531762303 | snp | C/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29035339 | AACAGATTTTTACGT[C/G]TTAAAAATCATTTTC | 10600 |
rs532045831 | snp | C/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29047387 | TGCACTGCATAGGTA[C/G]AGTACTCCTAATTGT | 10600 |
rs532099046 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29024937 | TCTCATTGGCTGCAT[A/G]TTCTGTCAGTTCCAG | 10600 |
rs532118396 | snp | C/T | | | upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29023948 | ATATTTGAAAATCCC[C/T]TCCTCCCCCGCAATT | 10600 |
rs532318745 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29043085 | TAAAAAAGAATACAC[C/G/T]GTGGTGACTTACATA | 10600 |
rs532364598 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP16 | GRCh38.p7 | 21:29040291 | CAGACCCTGTGGCTG[C/T]CATGTAATCATTGTG | 10600 |
rs532425756 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP16 | GRCh38.p7 | 21:29046568 | AAAACTGGATATAGT[A/G]CATGTGTGTGTTTTG | 10600 |
rs532436497 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | USP16 | GRCh38.p7 | 21:29054507 | TGTTTTATTACTGGG[A/G]AGATTTTAACTTCTA | 10600 |
rs532469368 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | USP16 | GRCh38.p7 | 21:29033018 | GTCAGTTAAAAAAAT[C/G]TGTATGTTAGAAAAG | 10600 |
rs532493515 | in-del | -/GGTGGGGT | 0.000244828 | 0.0110614 | upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29024599 | GTCCCGGGAGGTGGG[-/GGTGGGGT]GGTGGTGGCCTAGCC | 10600 |
rs532603798 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP16 | GRCh38.p7 | 21:29025835 | CTGCTATGTACTAAC[A/G]TTATGCTAGATATTA | 10600 |
rs532780939 | snp | A/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29034624 | GCCTAGCGAGTGCAT[A/G]GTTTTCTAAATACTT | 10600 |
rs532841961 | snp | C/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29029974 | ACAAAGTTCATAGGA[C/T]ATATTTAATTAATAT | 10600 |
rs532875888 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29048911 | CCTACTTTATTACCT[A/G]TTTTTTTCATTACTG | 10600 |
rs532933057 | in-del | -/C | | | intron-variant | USP16 | GRCh38.p7 | 21:29053368 | TGCTTCTCACCAACT[-/C]CCTTGGGGACATTTA | 10600 |
rs533040933 | snp | A/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29050538 | CATGTTGGTGGTTCA[A/G]GAATGGCTTTGTAAA | 10600 |
rs533110138 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29042585 | CCTGTAAGATTTTGT[C/G]GGGGGAAGCCTTGTT | 10600 |
rs533656390 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29051451 | AAAAGGAGATGGCCA[A/G]TGACAGGACCCTCCT | 10600 |
rs533697405 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29050733 | CAAGGTTATAGGGAG[A/G]GTTGAGAAATGAAGC | 10600 |
rs533804478 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29026671 | ACAGGCGTGAGCCAC[C/T]GCACCCAGACAACAT | 10600 |
rs533835726 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29039651 | TTACGAGTTAAAACA[A/G]TGAAAGCTAGTTATT | 10600 |
rs533845407 | snp | G/T | 1.65364e-05 | 0.0028754 | missense | USP16 | GRCh38.p7 | 21:29047254 | TGAGAAACTTCGAGA[G/T]GCGAATAAACTGCTT | 10600 |
rs534122018 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29033292 | TGATCTCAAATGATG[C/T]TGTAATTTTCAAAAA | 10600 |
rs534185192 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29042357 | TCAAATTTTCTTAAG[C/G]CTTTGTTTATTTTAA | 10600 |
rs534211359 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29027006 | ATATGATAAAAATGG[C/G]ATAACTGGGAGATGA | 10600 |
rs534312092 | snp | A/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29030224 | AGTGCCTGCCCTATA[A/G]TAGGTGTATTATTGA | 10600 |
rs534319791 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29042762 | AAGTAATTAGTTTGA[C/T]TGGTTTCCATACAGT | 10600 |
rs534449271 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29035314 | AGATGCTGCATTGTA[A/T]CATCATTAAAACAGA | 10600 |
rs534458599 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29028033 | GAATATGTTTTAAAA[G/T]GTAAAAATGGTATAA | 10600 |
rs534489172 | snp | C/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29025603 | CGTCTTTCAAGTTTT[C/T]CTATGGAGTCTAAGC | 10600 |
rs534795885 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29044515 | GCAAATGGCGAGATC[C/T]TGGCACACTGCAACC | 10600 |
rs534834298 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | USP16 | GRCh38.p7 | 21:29051601 | TTTGGGAGGCCGAGG[A/C]GGGTGGATCACTTGA | 10600 |
rs535107984 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29036154 | CAGAATTTTTACGTT[C/T]GGTTTCTTTAATAGA | 10600 |
rs535145223 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | USP16 | GRCh38.p7 | 21:29043881 | TAATATTATTGACAT[C/G]CACAAATTTAAAAAT | 10600 |
rs535240208 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP16 | GRCh38.p7 | 21:29034193 | GAGGCTGAAGTTAGG[A/G]GAATGTTTAGGAGAC | 10600 |
rs535307887 | snp | A/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29041901 | AGAAGTCTGTGGGAC[A/G]GGAAATTTAAAATAA | 10600 |
rs535311511 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29031092 | ACCTGTGCATAGACC[A/G]GTCATTGGATGTGGC | 10600 |
rs535656050 | snp | C/T | 7.38334e-05 | 0.00607546 | intron-variant | USP16 | GRCh38.p7 | 21:29028005 | TGAATCTTTAATGTT[C/T]ATATCTCTAAATGAA | 10600 |
rs535675214 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP16 | GRCh38.p7 | 21:29035468 | AACCTCCGCCTCCCA[C/G]GTTCAAGCAATTCTC | 10600 |
rs535909691 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29050865 | GGGGTGGCATGGTCA[C/G]ATCTTCATATGACGT | 10600 |
rs535918828 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29043008 | CTTGGCAATTAAAGT[C/G]TCACCAAATTTTATT | 10600 |
rs536000939 | snp | A/G | 1.72764e-05 | 0.00293903 | intron-variant | USP16 | GRCh38.p7 | 21:29050203 | AGTGGTCTTTTTCAG[A/G]AAAGTCCTTTAAAGT | 10600 |
rs536073047 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | USP16 | GRCh38.p7 | 21:29031927 | AACAACACACCAATC[A/G]CAATCAGATCTCCTG | 10600 |
rs536101929 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29045276 | ATTACAGAGTAGCCT[C/G]ACAGGGGCTGTTCTT | 10600 |
rs536126138 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | USP16 | GRCh38.p7 | 21:29029253 | CCCGTCTCTACTAAA[A/C]ATACAAAAAATTAGC | 10600 |
rs536201018 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29052224 | ACCACATTTTGAATA[A/G]CAATGGTCTAGACTG | 10600 |
rs536250361 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP16 | GRCh38.p7 | 21:29038046 | GCAAATACGTACCTA[C/T]AGGTAGTGGTAAGTG | 10600 |
rs536268801 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29045930 | CCTGCCTCAGCCTCC[C/T]GAGTAGCTGGGATTA | 10600 |
rs536328968 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29031759 | TTTTTGTTTTTTCAC[A/G]TTTTCAAATTGAAAA | 10600 |
rs536388662 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP16 | GRCh38.p7 | 21:29038525 | TCATTTCCACTGTTT[C/T]TGTTTGTTTTGTTTT | 10600 |
rs536662924 | snp | A/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29046482 | TGATCCTTGATAGCA[A/G]AGGAACTTTTTAGGA | 10600 |
rs536668682 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29036112 | ATAATAAACCAGAGT[G/T]AATATGCATAGTCTT | 10600 |
rs536702809 | snp | C/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29043922 | AAACAATAAGTCCCC[C/T]TCCCACCACTGTTTT | 10600 |
rs536727035 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29023658 | CAGGCTGGAGTGCAA[C/T]GGAGTGATCTTGGCT | 10600 |
rs536810383 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29025214 | TGATATACGCAAAAC[G/T]TGAAAGCCACGTTAA | 10600 |
rs536925455 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29053191 | AAGGGCCGTGATGCC[C/T]GTTACGGACTTTTAC | 10600 |
rs536992319 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29051191 | GATAGGATATATAGG[A/G]AGAAAAGCAGGTTGA | 10600 |
rs537471705 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29044627 | TAACTTTTGTATTTT[C/T]AGTAAAGACAGGTTT | 10600 |
rs537524146 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP16 | GRCh38.p7 | 21:29030199 | TTTTGGGCTCCTGAG[C/T]GTCTAGCACAGTGCC | 10600 |
rs537596225 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP16 | GRCh38.p7 | 21:29037153 | TTTAAAATCAAATGG[A/G]TGGGTGGGTTGGAAA | 10600 |
rs537601093 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29023594 | CACAAAGTGTGCACT[C/T]ACATATTTTCTTTTT | 10600 |
rs537731675 | snp | G/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29038146 | TGAGGTGATGAATAA[G/T]CTCAGAACTGAAGTA | 10600 |
rs537793903 | snp | A/G | 0.000379704 | 0.0137734 | missense, utr-variant-5-prime | USP16 | GRCh38.p7 | 21:29039531 | GCCAGGAGCTGCTTC[A/G]CTACTTATTGGATGG | 10600 |
rs537806543 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29025975 | TATGGGATAAGGGGA[C/T]AAGATGACTAGAGCA | 10600 |
rs537810556 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29026215 | TGTAATCCCAGCACT[C/T]TGGGAGGCCGAGGCA | 10600 |
rs537869092 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29025364 | TTTGATTTAGATTTT[A/G]TATGGAGTCCTGCGA | 10600 |
rs537896627 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | USP16 | GRCh38.p7 | 21:29046141 | AATAACTTTTCTTCA[A/T]AATTTATTTTTTGAG | 10600 |
rs537984399 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP16 | GRCh38.p7 | 21:29053124 | GTACTAAGTTCTTCA[A/G]TGAATATGGAGGCAC | 10600 |
rs538050854 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | USP16 | GRCh38.p7 | 21:29038920 | AACTTTTAAATGGGG[A/C]AGTTCTGTCAGGAAC | 10600 |
rs538195885 | snp | C/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29029212 | AGGTCAGGAGATCGA[C/G]ACCATCCTGGCTAAC | 10600 |
rs538270108 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29023460 | CTGTTTACATATCTA[G/T]TTTTCTATAGCTATC | 10600 |
rs538528856 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29028421 | TGAGAGCCACTGCAC[C/T]TGACTTTCTACATCT | 10600 |
rs538530681 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29038732 | GTGACTTAAGAGCTG[C/T]GTAACCAAATAAATA | 10600 |
rs538582741 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | USP16 | GRCh38.p7 | 21:29046030 | GTTTTCACCATGTTG[A/G]CCAGGCTGGTTTCAA | 10600 |
rs538609838 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29032379 | TGGGACTACACCTGC[A/G]TGCCACCACTCCTGG | 10600 |
rs538670495 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29031822 | TCTAACAGATAATAC[A/G]GAGAAATCCCTATGC | 10600 |
rs538679666 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP16 | GRCh38.p7 | 21:29052398 | GGCAAGGAGGAGCAC[A/G]TCACATCTTACATGG | 10600 |
rs538733554 | in-del | -/ATCTC | 0.000798403 | 0.0199641 | upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29023291 | AATAAAACAAAAATT[-/ATCTC]AGCAGTAAAAAGCAA | 10600 |
rs538743813 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP16 | GRCh38.p7 | 21:29025275 | CATTTTTAATGGAAC[A/C]GAGTAGGCAGGGGAA | 10600 |
rs538843085 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29045346 | TTAGGCATTTCAGTA[A/G]CAGGAATCTTGATGA | 10600 |
rs538900700 | snp | C/G | 0.00199481 | 0.0315187 | downstream-variant-500B | USP16 | GRCh38.p7 | 21:29054887 | AAAGTGCTGGGATTA[C/G]AGGCTTGAGCCACCG | 10600 |
rs538985499 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29024731 | GGAGCTGGCTGCCCA[A/G]CCCAAAGGCCCATGA | 10600 |
rs539048497 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29039427 | ATTTTCTAAAAATAG[C/T]TTCAGAGCTTAGTAG | 10600 |
rs539078030 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29047324 | GCAAATATAAAAGGT[A/G]TTTTAATGCTCTCAC | 10600 |
rs539205508 | snp | G/T | 3.90831e-05 | 0.00442041 | intron-variant | USP16 | GRCh38.p7 | 21:29040723 | CTAAAACACTATAGT[G/T]GAATTCCTCTGTACC | 10600 |
rs539260737 | snp | A/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29051866 | CCAGTTGCTGTGATG[A/G]GCATAATGGAAGAGG | 10600 |
rs539605997 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29027200 | TAAAAAAGTGAAGAT[G/T]TGATGTGCAGCTAGA | 10600 |
rs539668021 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29034067 | TCGGGGTCAGAGGAT[G/T]TCAGGTTTGTTTATT | 10600 |
rs539744325 | snp | A/G/T | 0.000133915 | 0.00818174 | missense, upstream-variant-2KB, utr-variant-5-prime | USP16 | GRCh38.p7 | 21:29027953 | AAAACTGTTCCAATC[A/G/T]ATGATTCCTCTGAAA | 10600 |
rs539897459 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29049280 | CATCTTTTCTGGAAA[A/T]CTTTTGCTATAGCTG | 10600 |
rs539968775 | snp | A/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29034408 | ACCTCCGCCTCCTGA[A/G]TTCAAGCAGTTCTCC | 10600 |
rs540055010 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29050029 | GTCGGAGGGGACTTC[A/G]GTTTACTTAACCTGT | 10600 |
rs540056347 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29024860 | TTTCCGCCCCAACTT[A/C]GTTCTCTTCTTGAAG | 10600 |
rs540110471 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP16 | GRCh38.p7 | 21:29035412 | ACGGAATCTTTCTGT[C/T]GCCCAGGCTGGAGTG | 10600 |
rs540172735 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29042870 | TTCATAAATGTTAAA[C/G]AGTATTATTTTGTTT | 10600 |
rs540404547 | snp | A/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29052892 | TCCAGAGGCTGAGGC[A/G]GGAGGATCACTTGAG | 10600 |
rs540421949 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | USP16 | GRCh38.p7 | 21:29032597 | TGTGTATCAAGTTTG[C/T]TCTTTTTTTATTACT | 10600 |
rs540439483 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP16 | GRCh38.p7 | 21:29041032 | TATTATGTGGCGTGT[A/G]AAGATTTAGGGCAGA | 10600 |
rs540511698 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29034257 | AGTGTGGTTTAATCT[A/G]GGCTGGAAAGTTGGA | 10600 |
rs540561163 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29025494 | CTCTCCTCATGACTC[A/G]TTAGTTGCCTTTATA | 10600 |
rs540573126 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | USP16 | GRCh38.p7 | 21:29033529 | GAAGATATGTTTCTC[A/C]GCAGTGATCTGACTA | 10600 |
rs540921340 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | USP16 | GRCh38.p7 | 21:29050279 | TGAAGTTGATAACAC[A/T]TATTGAGTAGAGTGG | 10600 |
rs541043859 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29027608 | ATCTGTGTAAGATGA[A/C]CAAGGTTCTCTCCTG | 10600 |
rs541139718 | snp | C/T | 9.90377e-05 | 0.00703627 | missense | USP16 | GRCh38.p7 | 21:29042518 | TGTCCCTCCCAGTTT[C/T]AGATGATCAGGTAAG | 10600 |
rs541292322 | snp | A/G | 0.000133918 | 0.00818176 | intron-variant | USP16 | GRCh38.p7 | 21:29042575 | GATTTTTTTTCCTGT[A/G]AGATTTTGTGGGGGG | 10600 |
rs541355770 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29049600 | AGTCTTGTTCTGTCA[C/T]CCAGGCTGGTGTGCA | 10600 |
rs541646067 | snp | A/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29039362 | GTTAATGGACTAAAC[A/G]GAAATTTGTAGAAAC | 10600 |
rs541743360 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP16 | GRCh38.p7 | 21:29038942 | GTCAGGAACATTGGT[A/G]GTATATGTTAACTAA | 10600 |
rs541829199 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29032240 | TTGGCTTTTGCTTTT[C/T]TCTTTTTTTGAGGCA | 10600 |
rs541851987 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29025680 | CAGACTTCTGACTTC[C/T]CATTTTTCACCCTTT | 10600 |
rs542051832 | in-del | -/A | 0.496105 | 0.0439572 | intron-variant, upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29026456 | GCAAGACTCCGTCTC[-/A]AAAAAAAAAAAAAAA | 10600 |
rs542289479 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29043323 | AAAAAAAAAGCTAAT[A/G]CATAATAGAAGTAGA | 10600 |
rs542308025 | snp | A/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29047653 | CAGGACGCCACACTT[A/G]AATTTATCAGTGAAC | 10600 |
rs542319988 | snp | G/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29041665 | GGAACTAGGCTGTCA[G/T]TCAGCCTACTCTGAG | 10600 |
rs542331648 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29051278 | ATACCTTTGAGAAAT[G/T]AATGTGCTTAGTCTA | 10600 |
rs542405985 | snp | A/G | | | upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29023269 | TCAATAAATAAATAA[A/G]TAAGTAAATAAAACA | 10600 |
rs542538927 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29036551 | AGGGATATGAGAAAT[C/G]ATCTAGTCAGATGTG | 10600 |
rs542658841 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29030360 | GTAGTGGGGGACAGT[A/G]GTGGTTATATTTAGG | 10600 |
rs542659066 | in-del | -/CT | 0.002622 | 0.0361126 | intron-variant | USP16 | GRCh38.p7 | 21:29048734 | AAAATGATTTTCTCC[-/CT]GTTAAAAATTTCTTC | 10600 |
rs542791842 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29022970 | CAGAATACAGAGAAA[C/G]ATGAAACTAAGCCGG | 10600 |
rs542869233 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | USP16 | GRCh38.p7 | 21:29029408 | ACAGAGCAAGACTCC[A/G]TCTCAAAAAGAAAAA | 10600 |
rs542884826 | in-del | -/AAGT | 0.00119737 | 0.0244387 | intron-variant | USP16 | GRCh38.p7 | 21:29047901 | ACATATAGAGACAAA[-/AAGT]AAGCCTGTGTGTGTG | 10600 |
rs542923579 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | USP16 | GRCh38.p7 | 21:29050449 | GAGCAGATCTATTAA[-/T]GAATAATCTGTTTAA | 10600 |
rs542999656 | snp | A/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29052351 | GGTTTACAGTTCCAC[A/G]TGGCTGGGGAGGCCT | 10600 |
rs543083313 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29049630 | AATGACACGATCATG[A/G]CTCACTGAAGGTTTG | 10600 |
rs543154411 | snp | C/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29052589 | GTGGGAGCTACAACT[C/T]AAGATGAGATTTGGG | 10600 |
rs543294078 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29045493 | GGCCATTTTTTTCCC[A/G]GAATACTTTTGTCCA | 10600 |
rs543369683 | snp | C/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29048284 | GATAGGGTTTCGCCA[C/G]GTTGGCCAGGGTGGT | 10600 |
rs543460012 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29036403 | TTTCTTTAATATACA[C/G]CAAATGTCGATTTGT | 10600 |
rs543601675 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP16 | GRCh38.p7 | 21:29038267 | TTGATAGAATAGACA[C/G]TTAAGAAGTGTCAGA | 10600 |
rs543614040 | snp | A/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29035357 | AAAAATCATTTTCAC[A/G]GTAGTCTTCACTGAA | 10600 |
rs543669306 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29035828 | GGAGGCTGAGGTAGG[A/C]GAATGGCATGAACCA | 10600 |
rs543731369 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29043291 | AATTTTGTCTCATCT[A/G]TTTTCAAATATTGTG | 10600 |
rs543843262 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP16 | GRCh38.p7 | 21:29029035 | AGGCCCCCTATTAGC[A/G]TAGTAAAGTGCCCAT | 10600 |
rs544052316 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29022701 | CTGCATTTCTGGAGC[C/T]TGGAGAAGAAAGCTT | 10600 |
rs544081750 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29031503 | GAGTGCAGTGGCACA[A/G]TCTTGGCTCATGGCA | 10600 |
rs544081872 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29024792 | GGTGAGTTCTGGTCC[C/T]ACTGCCTGGCAGTCG | 10600 |
rs544100898 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP16 | GRCh38.p7 | 21:29051952 | TGATCATTTATTATA[C/T]TTTTGTTTCTTGGCA | 10600 |
rs544216381 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29027680 | CACTTTCCTATGCTA[C/T]GAAAAACGGGAGATA | 10600 |
rs544270538 | snp | C/T | 0.000461331 | 0.0151807 | synonymous-codon | USP16 | GRCh38.p7 | 21:29054115 | CATCAGCGACACACA[C/T]GTGCAAGCTGTGCCT | 10600 |
rs544272533 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | USP16 | GRCh38.p7 | 21:29046384 | TCAAGTGATCCTCTT[G/T]TGATCATCTTGCTTT | 10600 |
rs544291072 | snp | C/T | | | upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29023323 | CAAGAGAGCTAGTTT[C/T]CCCCCAAATTTAACC | 10600 |
rs544309691 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29053396 | TTAAAGATGTAAGGG[A/G]TAATTTTTGGCACAA | 10600 |
rs544324166 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP16 | GRCh38.p7 | 21:29037648 | TGGAGTGCAGTGGCA[C/T]GATCGTGGCTCACTG | 10600 |
rs544367409 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP16 | GRCh38.p7 | 21:29045421 | GAGTGATTTTAAAGG[A/G]AAAAGTTCTTTACTC | 10600 |
rs544385420 | snp | A/C | 1.65345e-05 | 0.00287524 | missense | USP16 | GRCh38.p7 | 21:29046926 | AAGTAGATATGAAAA[A/C]TATCAACATGGATAA | 10600 |
rs544544768 | snp | C/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29031959 | GTTTGACTTCTTTTT[C/T]TGTGCATGTGTGTAT | 10600 |
rs544545633 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29032744 | TGTGTACAGGTTTTT[G/T]TGTGAACTTAGATTT | 10600 |
rs544607065 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29040082 | ACTAATATTTATTTC[G/T]CACTTATTTTTATGC | 10600 |
rs544731499 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29044848 | TCTATTGATTTAGGT[G/T]GTTTCTAGTATTTTG | 10600 |
rs544774068 | snp | A/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29034670 | CTCAGTTGCCTGTGC[A/T]TATGTAAGTTTTAAC | 10600 |
rs544902079 | snp | A/C/G | 1.65578e-05 | 0.00287726 | intron-variant | USP16 | GRCh38.p7 | 21:29034797 | CTCCCCTCTTGCTGA[A/C/G]TTTTTATGGCTTTGA | 10600 |
rs544969151 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | USP16 | GRCh38.p7 | 21:29051344 | CAGAGAGGTTAGGAT[C/G]GGCCCAGGGCACAGA | 10600 |
rs545068658 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29052701 | AGGTTAAAGAGTACA[A/G]AATAGGTGAGATGAG | 10600 |
rs545129712 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29044171 | ACTCCTGACCTCAAG[C/T]GATCCTCCCTCCTCA | 10600 |
rs545175251 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29053263 | AGAGAATGCCTGTTC[C/T]TGTTGCCAGCCCTAT | 10600 |
rs545274702 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29023165 | CAGCCACTGGGGAGG[A/G]TGAGGTGGGAGAATC | 10600 |
rs545408740 | snp | C/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29043786 | TATATGTGAAGAAAA[C/T]GTCGTGCTTCTTTTT | 10600 |
rs545823603 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29032106 | ATCATACCCACCTCC[C/T]TACTGCCACCACTCT | 10600 |
rs545858011 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29047891 | TTATTTATTTACATA[C/T]AGAGACAAAAAGTAA | 10600 |
rs545966590 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29032637 | TTATGGCATATAGTA[C/G]AACAGCTTGTTTTTA | 10600 |
rs546012971 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29041137 | CGTGTGGCGCCTGAA[A/G]TGTGACTGGTGAAAC | 10600 |
rs546125166 | in-del | -/T/TT | | | intron-variant | USP16 | GRCh38.p7 | 21:29044448 | AAACTTCTTCATTCT[-/T/TT]TTTTTTTTTTTTTTT | 10600 |
rs546135580 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29027728 | AGTTCCTGTTGAAAA[C/T]TAGATGATTATATGT | 10600 |
rs546290943 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29030993 | GCATAGGGAGAAGTT[A/G]AATGAAGAGGCAGTG | 10600 |
rs546426078 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29023351 | ACCAAATGTTACTCT[C/G]GTGGTTAGTATGCCA | 10600 |
rs546581145 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29052967 | CTCCAGCCTGGGTGA[C/T]GGAGTGAGACCCTGT | 10600 |
rs546586448 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29038631 | GTGCTCTGTTTTTCT[A/G]TGCTCGAGTGTTAAG | 10600 |
rs546662051 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29032348 | GTGATCCTCCCACCT[C/T]AGCCTCCTGAGTAGC | 10600 |
rs546890090 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29025257 | AAGTTTTCCACACGC[C/T]TACATTTTTAATGGA | 10600 |
rs546950721 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP16 | GRCh38.p7 | 21:29046486 | CCTTGATAGCAAAGG[A/G]ACTTTTTAGGATCAG | 10600 |
rs547069727 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | USP16 | GRCh38.p7 | 21:29054769 | AGGCGCCCGCCACCA[C/T]GCCCAGCTAATTATT | 10600 |
rs547317218 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29025816 | AGAAGTATTTCTTCA[A/G]GACCTGCTATGTACT | 10600 |
rs547344827 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29027128 | AATTCTATATAATTA[A/G]GTAGACCTGTATGTA | 10600 |
rs547434911 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | USP16 | GRCh38.p7 | 21:29048071 | TGTGTGTGTGTGTGT[A/G]TGTGTGTGTGTGTGT | 10600 |
rs547625352 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29028369 | TGGCCTCAAGTGATC[C/T]GCCTGCCTTGGCCTC | 10600 |
rs547739455 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29050702 | GGTAACGTATGTAGT[C/T]CTAGAGTTTATAGTA | 10600 |
rs547747916 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29034050 | AACACTGGAGAGATA[C/T]GTCGGGGTCAGAGGA | 10600 |
rs547750988 | snp | A/C | | | intron-variant | USP16 | GRCh38.p7 | 21:29053426 | ACCTAAAATACTGTT[A/C]TCTTCCTGTTCAGGG | 10600 |
rs547781278 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29027820 | ACTGTCTCCTAGAGA[A/C]ATATAAGACATACTT | 10600 |
rs548004389 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29053670 | GTATGGAGAAAAGAG[G/T]AGACTCATGAATGAT | 10600 |
rs548402104 | snp | C/T | 0.00199481 | 0.0315187 | downstream-variant-500B | USP16 | GRCh38.p7 | 21:29054713 | TGCCTCCTAGGTTCA[C/T]GCCATTCTCCTGTCT | 10600 |
rs548604197 | in-del | -/TTGG | 0.00159617 | 0.0282053 | intron-variant | USP16 | GRCh38.p7 | 21:29042762 | AAGTAATTAGTTTGA[-/TTGG]TTTCCATACAGTGAA | 10600 |
rs548681515 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29042745 | TATTCAGAATTCTGT[A/C]CAAGTAATTAGTTTG | 10600 |
rs548708659 | snp | A/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29050867 | GGTGGCATGGTCAGA[A/T]CTTCATATGACGTAG | 10600 |
rs548760109 | snp | A/T | | | intron-variant, utr-variant-5-prime, upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29024953 | TTCTGTCAGTTCCAG[A/T]AGCTGGCCAATGAGA | 10600 |
rs549014231 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29035272 | CTATGAATTTGCATG[A/G]AAATAAATGTCAGTC | 10600 |
rs549035209 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP16 | GRCh38.p7 | 21:29029141 | CCTTCTGACCAGGTG[C/T]GGTGGCTCACGCCTG | 10600 |
rs549171776 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP16 | GRCh38.p7 | 21:29051572 | GTGGTGGCTTACGCC[C/T]GTAATGCCAACACTT | 10600 |
rs549361337 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP16 | GRCh38.p7 | 21:29048163 | TTTCAGCTCACTGCA[A/G]TCTCCACCTCCCGGG | 10600 |
rs549460140 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29050878 | CAGATCTTCATATGA[C/T]GTAGGTTACTTGTTG | 10600 |
rs549473342 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29048927 | TTTTTTTCATTACTG[G/T]CTCAACATACTACTT | 10600 |
rs549576413 | snp | C/G | | | intron-variant, upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29026168 | GAGTGGAGTACAAGA[C/G]AAGGACTTGGCCAGG | 10600 |
rs549639528 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | USP16 | GRCh38.p7 | 21:29045183 | CTTATTTTTTATTCA[C/T]GTGTTCCTCTGTTTT | 10600 |
rs549672689 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29037726 | GAGTAGCTGGGACTA[C/T]AGGCATGCGCCACCA | 10600 |
rs549677388 | snp | C/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29035758 | CATCTCTACTAAAAA[C/T]ACAAAAAAAAAGTAG | 10600 |
rs549735040 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29036814 | CAGCATTTGCTTTAA[A/G/T]CATGTTTTTTAAGTT | 10600 |
rs549735429 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29045010 | GACAGCTGTGTGTTA[C/T]CAAACTTCCAGATTT | 10600 |
rs549801970 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29042187 | AAAGCAGAAATCTCT[A/G]CCTTCATAGGATATC | 10600 |
rs549938843 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | USP16 | GRCh38.p7 | 21:29034609 | GGTGTGAGCCACCGC[C/G]CCTAGCGAGTGCATG | 10600 |
rs549982000 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29041714 | TGGAGAGAGAGAGAA[A/G]GACATAGAAGTCTCA | 10600 |
rs550067226 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29028448 | ATCTTTTTTGTTTTT[C/T]TTCCTGAGACGGAGT | 10600 |
rs550366556 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29023282 | AAATAAGTAAATAAA[A/T]CAAAAATTATCTCAG | 10600 |
rs550395418 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29050778 | AGGAATGAAGTTTTG[A/G]AGGGTTCTCATGGTG | 10600 |
rs550459652 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29043789 | ATGTGAAGAAAACGT[C/T]GTGCTTCTTTTTTTT | 10600 |
rs550466229 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP16 | GRCh38.p7 | 21:29044333 | GCAAATACAAATATG[C/T]AGTCTTGGTTTTTTT | 10600 |
rs550595899 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29052201 | ATGCTGATGCTGGCT[G/T]TTCATGGACCACATT | 10600 |
rs550671363 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29045700 | TTAGTACTCTGCCTG[A/G]ATTACTTCCCTTAGC | 10600 |
rs550939230 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29046302 | CCAACGTGCCCAGCT[A/G]ATTTTTATTTTTATT | 10600 |
rs551031265 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP16 | GRCh38.p7 | 21:29029209 | ACGAGGTCAGGAGAT[C/T]GAGACCATCCTGGCT | 10600 |
rs551033366 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29036673 | ACTGTTCTTACTGTC[A/G]TACATTTTGTAATAG | 10600 |
rs551069505 | snp | A/G | 4.98335e-05 | 0.00499142 | missense | USP16 | GRCh38.p7 | 21:29043516 | GATAACGACAGTTAC[A/G]TAAAAGAGAGAAGTG | 10600 |
rs551170044 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29029566 | TAATTATGCCACTTG[A/T]CTAGTTTCTAAACCT | 10600 |
rs551176952 | in-del | -/T | 0.00199481 | 0.0315187 | intron-variant | USP16 | GRCh38.p7 | 21:29039288 | ATACAAAAGGCATAG[-/T]TTTTTTTTCATTTGG | 10600 |
rs551322500 | snp | A/C | 0.00254129 | 0.0355554 | upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29024592 | GCCGATGGTCCCGGG[A/C]GGTGGGGGTGGGGTG | 10600 |
rs551464158 | snp | G/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29031551 | TCAAGCAGTTTTCCT[G/T]CCTCAGTCTCCAAGT | 10600 |
rs551465877 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29052159 | TGGGATCAAAAATTC[C/T]GCATGTTTAATGTAA | 10600 |
rs551553244 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | USP16 | GRCh38.p7 | 21:29045157 | TTTGAAGTTTTTGCT[A/T]ATATTCTTTTCTTAT | 10600 |
rs551676567 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29037942 | AGTTTGGTGAGCACT[C/T]GGGTGCAGTGGGTTT | 10600 |
rs551746325 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29051616 | CGGGTGGATCACTTG[A/G]GGTGAGGAGTTCGAG | 10600 |
rs551748441 | snp | A/T | 0.00874735 | 0.0655527 | intron-variant | USP16 | GRCh38.p7 | 21:29050280 | GAAGTTGATAACACT[A/T]ATTGAGTAGAGTGGG | 10600 |
rs551799085 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29029542 | GTGCAAGATCATTGG[A/G]CATAAAGCTAATTAT | 10600 |
rs551800374 | snp | C/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29041091 | GGAACTCCTCTATAC[C/T]TTTGCTGTTCCATAT | 10600 |
rs552084260 | snp | C/T | 0.000364732 | 0.0134994 | intron-variant | USP16 | GRCh38.p7 | 21:29038308 | CTTTAAATAATTTTT[C/T]TCTTTTTTTTTCACC | 10600 |
rs552135725 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29031110 | CATTGGATGTGGCCT[G/T]CCCCTAGAGCAGGAA | 10600 |
rs552195659 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29046612 | ATCTCTCTTCCTCCT[C/T]TTCTCCCGCTCTTTC | 10600 |
rs552220643 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29025912 | CTTTAGATTCTGCTT[A/G]CAGAAATAACATAAA | 10600 |
rs552222964 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29033762 | AGTACAAGGTAAAAA[A/G]TAAGGAATGCCACTA | 10600 |
rs552345872 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29024941 | ATTGGCTGCATGTTC[C/T]GTCAGTTCCAGAAGC | 10600 |
rs552395057 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29053588 | TGGCCTGTGGCTTAC[A/T]GCTTTTCTACCAGGG | 10600 |
rs552508252 | snp | A/G | 0.00199481 | 0.0315187 | downstream-variant-500B | USP16 | GRCh38.p7 | 21:29054636 | TTTTTTTTTTGAGAC[A/G]GAGTCTTGCTCTGTC | 10600 |
rs552536753 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | USP16 | GRCh38.p7 | 21:29040379 | CTTTGGCTTGAAGAG[G/T]TTTAAGATCTTGAAA | 10600 |
rs552740537 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29044791 | TTTTAACAGTTGCAT[A/G]ATTCTGTGTTATGGA | 10600 |
rs552942874 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29022638 | GACAGGAAGCACGTG[G/T]TACAATGACCCTAAG | 10600 |
rs553088741 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29031259 | ATCTTTGGCAGTGAG[A/G]GCATGTCTGGCTGGC | 10600 |
rs553328371 | snp | C/G | 3.30929e-05 | 0.0040676 | missense | USP16 | GRCh38.p7 | 21:29047015 | GAAGGGAGCAATGGA[C/G]AAGTGGACATTTCCA | 10600 |
rs553405034 | snp | A/T | 0.000798403 | 0.0199641 | utr-variant-5-prime, upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29024672 | TTCCAGGGGTCACTC[A/T]GGCTTCGACTCCGTC | 10600 |
rs553408500 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP16 | GRCh38.p7 | 21:29053196 | CCGTGATGCCTGTTA[C/T]GGACTTTTACATGAG | 10600 |
rs553475873 | snp | G/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29037952 | GCACTCGGGTGCAGT[G/T]GGTTTGAAAGAAATA | 10600 |
rs553517402 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29051723 | GTAATCCCAGCTACT[C/T]GGGAGGCTGAGGCAG | 10600 |
rs553518546 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29046288 | ACTACAGGTGGACAC[C/T]AACGTGCCCAGCTAA | 10600 |
rs553679303 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29025544 | GGCTCTTTCCGCAGC[A/G]CTGGAGTGACCCCTC | 10600 |
rs553836572 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP16 | GRCh38.p7 | 21:29028727 | GGCGTGAGCCACCGC[A/G]CCCGACCTTCAACAA | 10600 |
rs553860789 | snp | A/T | 3.47114e-05 | 0.00416587 | missense | USP16 | GRCh38.p7 | 21:29040624 | AGAGTGAGTAAAGGA[A/T]TACTTAAAGCATTTG | 10600 |
rs553862493 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | USP16 | GRCh38.p7 | 21:29032599 | TGTATCAAGTTTGCT[C/T]TTTTTTTATTACTGA | 10600 |
rs553941723 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29031228 | CTCAGCACCTGGGGG[A/G]ATGAGTAGTACCTTG | 10600 |
rs553947828 | in-del | -/A | 0.00199481 | 0.0315187 | intron-variant | USP16 | GRCh38.p7 | 21:29030325 | TTAAAGGAAATAGCC[-/A]AATAAATTGAAATGA | 10600 |
rs554063474 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP16 | GRCh38.p7 | 21:29034260 | GTGGTTTAATCTGGG[C/T]TGGAAAGTTGGACAA | 10600 |
rs554066817 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29049139 | AAAGAAAAAGACTGG[C/T]GTGTTACATATATCT | 10600 |
rs554187775 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29042358 | CAAATTTTCTTAAGC[C/G]TTTGTTTATTTTAAA | 10600 |
rs554325417 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29041673 | GCTGTCATTCAGCCT[A/C]CTCTGAGCTGTTCAT | 10600 |
rs554374768 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | USP16 | GRCh38.p7 | 21:29048441 | TGATGGAATATACTA[A/C]ACTTTCAACCTCATT | 10600 |
rs554593755 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29053142 | AATATGGAGGCACAG[A/C]TTGGGAAGCTGAGTA | 10600 |
rs554734538 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29026565 | TTTTTTTTTTTTGGT[A/G]GAGATAGAGTGTCGC | 10600 |
rs554780437 | snp | A/G | 0.000258027 | 0.0113555 | intron-variant | USP16 | GRCh38.p7 | 21:29039610 | TATGATCTTATCTTC[A/G]TAAGCTTTCTGTCTC | 10600 |
rs554844274 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29048329 | CTCAAGTGATTTGCC[C/T]GCCTAGGCCTCCCAA | 10600 |
rs554866606 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29041018 | GCCAACTTAGTTCTT[A/G]TTATGTGGCGTGTAA | 10600 |
rs555016216 | snp | C/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29033788 | CACTAGGAATTCATG[C/T]CATGTTTTATAGAAT | 10600 |
rs555205342 | in-del | -/T | 0.00438332 | 0.0466095 | upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29023989 | GTCTTTCGGTTTTGC[-/T]TTTAAAAATTCACTC | 10600 |
rs555207246 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29034679 | CTGTGCATATGTAAG[C/T]TTTAACAAAATATTG | 10600 |
rs555342390 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29034201 | AGTTAGGGGAATGTT[C/T]AGGAGACTGTTAAGG | 10600 |
rs555409962 | snp | C/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29046596 | TTGTCCTTCTTCCTC[C/T]ATCTCTCTTCCTCCT | 10600 |
rs555474599 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29027527 | GATTAAAGTGCTGCC[A/G]TTATTTCACATGTAT | 10600 |
rs555666364 | snp | C/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29042816 | TTAATACTTATTTTT[C/G]TTATTTAAGACTAAT | 10600 |
rs555821168 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP16 | GRCh38.p7 | 21:29029282 | GCTGGGCGTGGTGGC[A/G]GGCGCCTGTAGTCCC | 10600 |
rs555858977 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP16 | GRCh38.p7 | 21:29035498 | CCTGCCTCAGCCTCC[C/T]GAGTAGCTGAGATTA | 10600 |
rs555861398 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | USP16 | GRCh38.p7 | 21:29043836 | TGTAACAAGTATTTG[C/T]AGTAAGTTTAATTAA | 10600 |
rs555927847 | snp | C/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29032289 | CAGGCTGGAGTTCAG[C/T]GGTATAATCACGGCT | 10600 |
rs556002467 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29041506 | GTTTGAAATATTTTC[C/T]TGAGGTTTTTCTTTT | 10600 |
rs556103635 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29040733 | ATAGTTGAATTCCTC[C/T]GTACCTTAGGACAAG | 10600 |
rs556182903 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29026225 | GCACTTTGGGAGGCC[A/G]AGGCAGGTGGATCAC | 10600 |
rs556195103 | snp | C/G | | | upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29023067 | GGAGTTCAAGACCAG[C/G]CTGGCCAATATGCTG | 10600 |
rs556225945 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29027530 | TAAAGTGCTGCCATT[A/G]TTTCACATGTATGTA | 10600 |
rs556387255 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29027319 | TGATACGCATAGGAA[A/G]TCCTGGTGTGGAAAA | 10600 |
rs556457674 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29042911 | CCTTTTAAATAGTAG[G/T]AGGAAAAAAGAAGAG | 10600 |
rs556467267 | snp | A/C | | | missense, utr-variant-5-prime | USP16 | GRCh38.p7 | 21:29034885 | TTGAAGCACTATCTG[A/C]CGCCAAGATCTGAAC | 10600 |
rs556531855 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29029230 | CATCCTGGCTAACAC[A/G]GTGAAACCCCGTCTC | 10600 |
rs556594194 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP16 | GRCh38.p7 | 21:29035442 | GCAGTGGTGTGATCT[C/T]GGCTCACCACAACCT | 10600 |
rs556695224 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29034832 | TATGATTATGATTTT[C/T]TTAGGGCTGTGGCAG | 10600 |
rs556698908 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29051213 | GCAGGTTGAGAAAAG[C/G]AGGTAGAGAAAGGAT | 10600 |
rs556756364 | snp | A/C/G | 0.00223321 | 0.0333414 | intron-variant | USP16 | GRCh38.p7 | 21:29042435 | TGTAACATTTACAGT[A/C/G]TTTACATTTTTACAC | 10600 |
rs556830516 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29050055 | CCTGTATTGCTTTTC[C/T]AAGAAAAGAAGTCAA | 10600 |
rs556862119 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP16 | GRCh38.p7 | 21:29051694 | AAATTAGCCAGGCAT[A/G]GTGGTGTGCGCCTGT | 10600 |
rs556972599 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29044664 | GTTGGTCAGGCTGGT[C/T]TCTAACTCCTGACCT | 10600 |
rs557049582 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29037167 | GGTGGGTGGGTTGGA[A/G]AGAATGACTTCAGGT | 10600 |
rs557385230 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP16 | GRCh38.p7 | 21:29038057 | CCTACAGGTAGTGGT[A/G]AGTGGTTGTGAGAGA | 10600 |
rs557444536 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29022801 | CCGTGGATATGCCCA[G/T]GATTTGACTTGGGCC | 10600 |
rs557577046 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29023597 | AAAGTGTGCACTTAC[A/G]TATTTTCTTTTTTTC | 10600 |
rs557860939 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | USP16 | GRCh38.p7 | 21:29043890 | TGACATCCACAAATT[A/T]AAAAATATATAAAGG | 10600 |
rs558238067 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29029346 | TGAACCTGGGAGGCG[A/G]AGCTTGCAGTGAGCC | 10600 |
rs558240034 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29037052 | GTTTGGTTTCATTTA[C/T]CAAACTAATGCTTAC | 10600 |
rs558452648 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29038182 | GACCCAAATAGAGTA[A/G]GGAGAGAAGCATCTG | 10600 |
rs558486621 | snp | C/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29052770 | ATAAGATTTATGTCC[C/T]TTCAGCTCAGGAGTT | 10600 |
rs558504197 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP16 | GRCh38.p7 | 21:29045359 | TAACAGGAATCTTGA[C/T]GAAATGCCTTCTTTT | 10600 |
rs558546069 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29051779 | GAGCTGCAGTGAGCC[A/G]AGATTGCGTCACTGC | 10600 |
rs558655401 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29025336 | GAATAATATGAGAAC[C/G]GGCAAGACTATCTTT | 10600 |
rs558707813 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP16 | GRCh38.p7 | 21:29052421 | TTACATGGATGGCAG[C/T]GGGCAAAGCAAGAGC | 10600 |
rs558712470 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29046056 | TTCAAACTCCTCACC[C/T]CAAGTGAGATGCCCT | 10600 |
rs558822149 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29053102 | AGAATCATAGATGGA[C/T]GGAGAAGTACTAAGT | 10600 |
rs558826545 | snp | A/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29031915 | TATTGAGATTGAAAC[A/T]ACACACCAATCGCAA | 10600 |
rs558844233 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | USP16 | GRCh38.p7 | 21:29054903 | AGGCTTGAGCCACCG[C/T]GCTGGGCCATACAAG | 10600 |
rs558949013 | in-del | -/TG | 0.00159617 | 0.0282053 | intron-variant | USP16 | GRCh38.p7 | 21:29025867 | AGGCAGTTCCAAAAC[-/TG]TGCTTGAAACCATTT | 10600 |
rs558971626 | snp | C/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29046188 | CCACCCAGTTTGGAG[C/T]ATAGTGTGCATGATC | 10600 |
rs559009761 | snp | A/C/G | 0.000264316 | 0.0114931 | synonymous-codon | USP16 | GRCh38.p7 | 21:29046885 | AATGATCGAAAGTGT[A/C/G]ACTGACAATCAAAAA | 10600 |
rs559105622 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29036590 | CATAGACTAAGGTAA[A/T]GGCCATTAATGCTAA | 10600 |
rs559249868 | snp | A/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29038893 | TTTCTATCTCTTTTG[A/T]TGTACATTTTAAACT | 10600 |