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 |