SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs559415963 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29051320 | GATATACATATCTGA[A/G]ACCTATAGCAGAGAG | 10600 |
rs559557411 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29030464 | ATCAAACAATTTTAA[A/G]TTCAGAATATCTTAA | 10600 |
rs559577233 | snp | C/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29050035 | GGGGACTTCGGTTTA[C/G]TTAACCTGTATTGCT | 10600 |
rs559808236 | in-del | -/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29040174 | AGGTGGATACTGTGA[-/T]TTTTTCCTATTCCAT | 10600 |
rs560011048 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29024476 | AGCATTTATATAACT[G/T]CGTGGTTATGTCAGA | 10600 |
rs560013613 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29045512 | TACTTTTGTCCATTC[C/G]TCTGACCAAAGCAGT | 10600 |
rs560171489 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29053559 | TGGTATCTGAGCCAG[C/G]TAACTGCATCAAGTG | 10600 |
rs560173027 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29031529 | TGGCAGCCTCCACCT[A/C]CCAGGTTCAAGCAGT | 10600 |
rs560173167 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29038958 | GTATATGTTAACTAA[G/T]TAGATTTTAGTAAAG | 10600 |
rs560206014 | snp | A/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29028719 | GGATTACAGGCGTGA[A/G]CCACCGCGCCCGACC | 10600 |
rs560293684 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29033666 | TGTGTTCTAGAATAT[C/T]TGGTAATAGATTAAG | 10600 |
rs560357496 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP16 | GRCh38.p7 | 21:29041111 | CTGTTCCATATAGAA[C/G]CAACTAGGCACGTGT | 10600 |
rs560357595 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | USP16 | GRCh38.p7 | 21:29033011 | CATTGTGGTCAGTTA[A/G]AAAAATCTGTATGTT | 10600 |
rs560455167 | snp | C/T | 0.000115778 | 0.0076076 | synonymous-codon | USP16 | GRCh38.p7 | 21:29047026 | TGGAGAAGTGGACAT[C/T]TCCAATGGTTTCAAA | 10600 |
rs560509383 | snp | A/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29042221 | TTAAACTATTCAGAT[A/G]CTATTCAGATGTGCA | 10600 |
rs560552148 | snp | C/G | | | upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29023989 | CGTCTTTCGGTTTTG[C/G]TTTAAAAATTCACTC | 10600 |
rs560574933 | snp | C/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29035215 | TAGTGGAGATAGGGA[C/T]GCTAAGAACAAATTT | 10600 |
rs560577718 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | USP16 | GRCh38.p7 | 21:29054468 | GATCACAACACATCA[A/G]TAAACTGACTTACCC | 10600 |
rs560580979 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29027636 | CTGACCTTTACATAT[A/G]TTGAAAACCTCTTAA | 10600 |
rs560709297 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29037672 | CTCACTGCAGCCTCT[A/T]CCTCTTGGGCTCAAG | 10600 |
rs560746949 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29024314 | TTCAAGACAACTTAG[A/G]TACTCAGTTTTAGAA | 10600 |
rs560844006 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29030857 | CCTGAAAGTACAGTA[C/T]GGATAAAAGGATACT | 10600 |
rs560845776 | snp | A/T | 0.0103295 | 0.0711199 | intron-variant | USP16 | GRCh38.p7 | 21:29043167 | CATGTATCTAATAAA[A/T]TTCGTTATATTTCTA | 10600 |
rs560856580 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29045456 | CTGTATGTGTGGCTA[A/C]CTTGCTTCTTTGCTA | 10600 |
rs560884194 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29024827 | TCGCCTGGCTTTCTG[A/C]GCTGGGAGAGCTCCT | 10600 |
rs560893665 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29044992 | AGGTTGCTCCTGACC[C/T]TTGACAGCTGTGTGT | 10600 |
rs560974612 | snp | C/T | | | upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29023362 | CTCTGGTGGTTAGTA[C/T]GCCACCATCTTAAAC | 10600 |
rs561000237 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP16 | GRCh38.p7 | 21:29031521 | TTGGCTCATGGCAGC[C/T]TCCACCTCCCAGGTT | 10600 |
rs561061781 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP16 | GRCh38.p7 | 21:29038229 | AAGTATAGAGTTTTC[A/G]GTGTTGGTCATGATT | 10600 |
rs561288372 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29053518 | CTCAGGCTCCTAAAG[A/C/T]AACTGGCAAGTTGAA | 10600 |
rs561382579 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29033480 | TTGTACTGTGATCCA[A/G]AAGTTGATAGACTGG | 10600 |
rs561393618 | in-del | -/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29049106 | CGATTGGCATCTTAC[-/T]TTTATTTCAGGTTAA | 10600 |
rs561455472 | snp | A/G | | | upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29024236 | ACAGAGGGATATTCC[A/G]TCTCAAACAAACAAA | 10600 |
rs561647871 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | USP16 | GRCh38.p7 | 21:29032829 | AATGTTTAGTTTTTT[A/G]AGAAACTGCCAAACT | 10600 |
rs561819091 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29048035 | CTGTATATATATCAG[C/T]TCAGAGACGATACGT | 10600 |
rs561978405 | snp | A/G | 8.51187e-05 | 0.0065232 | intron-variant | USP16 | GRCh38.p7 | 21:29048739 | GATTTTCTCCCTGTT[A/G]AAAATTTCTTCTTTT | 10600 |
rs562096926 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP16 | GRCh38.p7 | 21:29034494 | ATTTTTGTATTTTTA[A/G]TAGAGATGGGGTTTC | 10600 |
rs562231191 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29027793 | GCATAATATACGTGG[C/T]TTAGTTATATTACTG | 10600 |
rs562384268 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29039858 | GAGAGCTGCCAAATA[C/T]TGGAAATTGTTTCTC | 10600 |
rs562508201 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29032115 | ACCTCCCTACTGCCA[C/T]CACTCTCTGCAGCCC | 10600 |
rs562561553 | in-del | -/A | 0.00199481 | 0.0315187 | upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29024346 | CGACAGGACAGAATT[-/A]ACGGAAACAAATTTA | 10600 |
rs562646691 | snp | G/T | 0.000798403 | 0.0199641 | downstream-variant-500B | USP16 | GRCh38.p7 | 21:29054637 | TTTTTTTTTGAGACG[G/T]AGTCTTGCTCTGTCG | 10600 |
rs562690245 | snp | A/C | | | upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29023604 | GCACTTACATATTTT[A/C]TTTTTTTCTTTTTGA | 10600 |
rs562721156 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29027738 | GAAAATTAGATGATT[A/G]TATGTGATTGGTCTT | 10600 |
rs562723896 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | USP16 | GRCh38.p7 | 21:29035541 | ACCACGCCCGGCTAA[-/T]TTTTGTATTTTTAGT | 10600 |
rs562843017 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29041748 | ACTTGCACAGTTTAC[C/T]TCCCACTGACTAGAT | 10600 |
rs563056934 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29049672 | TCAAGCGATCCTCCC[A/C]CCTTAGCCTCTATAG | 10600 |
rs563067990 | snp | C/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29045544 | CTGTACTTGTGCATC[C/G]TTGAGTTTTCTTTCA | 10600 |
rs563168546 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | USP16 | GRCh38.p7 | 21:29050467 | ATAATCTGTTTAATG[G/T]GGTTGAATGTTAAGG | 10600 |
rs563435890 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29035885 | GATCCTGCCACTGCA[C/T]GCAGCCTGGGCAACA | 10600 |
rs563548919 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29042620 | TTTTTAAGTTTGTAT[A/G]TTACTAGCCCATGCA | 10600 |
rs563703102 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29043924 | ACAATAAGTCCCCCT[C/T]CCACCACTGTTTTTT | 10600 |
rs563854436 | snp | G/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29035168 | GAATCTTTACCCCTT[G/T]GTTTTTCTTGCTTGT | 10600 |
rs563990471 | snp | C/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29048422 | ATTTGCAAATGATTT[C/G]ATGTGATGGAATATA | 10600 |
rs564226957 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP16 | GRCh38.p7 | 21:29042583 | TTCCTGTAAGATTTT[A/G]TGGGGGGAAGCCTTG | 10600 |
rs564370367 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | USP16 | GRCh38.p7 | 21:29033092 | AATACATATGGTGAG[A/T]ATGAATATGCTTTGC | 10600 |
rs564455087 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29028370 | GGCCTCAAGTGATCC[A/G]CCTGCCTTGGCCTCC | 10600 |
rs564605028 | in-del | -/TTCT/TTCTTTCT | 0.0560604 | 0.158706 | intron-variant | USP16 | GRCh38.p7 | 21:29044748 | ACCGTGCCTGGCCCA[-/TTCT/TTCTTTCT]TTCTTTCTTTCTTTC | 10600 |
rs564685637 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29044230 | TGAGCCACCGCGCCC[A/G]GCCGACCACCACTTT | 10600 |
rs564717294 | snp | A/G | 9.11635e-05 | 0.00675081 | intron-variant | USP16 | GRCh38.p7 | 21:29030578 | ATATATTCCTTGTCT[A/G]TTATTTGTTTTAATA | 10600 |
rs564777911 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29029598 | CAGTGTTCCTGGAAC[A/T]ACTCAGCACTGTAGA | 10600 |
rs564832172 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | USP16 | GRCh38.p7 | 21:29036707 | GATTTCAGTCTGTCT[C/G]CTGGGATAACATAAA | 10600 |
rs564880718 | in-del | -/AAG | 0.00119737 | 0.0244387 | intron-variant | USP16 | GRCh38.p7 | 21:29052757 | ACTAAGACTAAAAAT[-/AAG]ATTTATGTCCCTTCA | 10600 |
rs564903465 | snp | C/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29035912 | AACAGAGCGAGACTC[C/T]GTCTCAAAAAAAACC | 10600 |
rs564921686 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | USP16 | GRCh38.p7 | 21:29051386 | GTACATATGTGGCAG[G/T]TTAAACTATGAGAAG | 10600 |
rs565013493 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29044918 | AGTCATCTGTAGGGT[A/C]AATTTTGAGAAGAGG | 10600 |
rs565026317 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29052755 | GGACTAAGACTAAAA[A/G]TAAGATTTATGTCCC | 10600 |
rs565053058 | snp | C/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29052947 | GCTGAGATCATGCCA[C/T]TGCACTCCAGCCTGG | 10600 |
rs565200359 | snp | G/T | | | upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29023936 | AATGGACAGTAAATA[G/T]TTGAAAATCCCCTCC | 10600 |
rs565294471 | snp | A/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29034563 | GGTGATCCCACCCCT[A/G]GCCTCAGCCTCCCAA | 10600 |
rs565300562 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29038319 | TTTTCTCTTTTTTTT[C/T]CACCCTACATTCTAG | 10600 |
rs565306799 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | USP16 | GRCh38.p7 | 21:29042755 | TCTGTACAAGTAATT[A/T]GTTTGATTGGTTTCC | 10600 |
rs565368257 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29042343 | TGTAATTTTTCATTT[A/C]AAATTTTCTTAAGCC | 10600 |
rs565388116 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29045607 | GACCCAGTAACTCAT[A/G]TGGATACATTTCTTT | 10600 |
rs565573891 | snp | C/T | 0.000399281 | 0.0141238 | missense, utr-variant-5-prime | USP16 | GRCh38.p7 | 21:29039053 | ATAAACCTTGAGCCT[C/T]CAGGCCCTCTTACTT | 10600 |
rs565713503 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29049885 | TTTCTTAATGTGTTG[G/T]TGTGTGTTTTTTGTG | 10600 |
rs565781902 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29028548 | TCAAGCGATTCTCCT[G/T]TCTCAGCCTCATGAG | 10600 |
rs565839071 | snp | A/G | 0.000222109 | 0.0105359 | intron-variant | USP16 | GRCh38.p7 | 21:29041976 | AATTAATTATATAAC[A/G]GTAATTGGTAATTGA | 10600 |
rs565904913 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29050918 | GGCTGAATTTTAGGA[C/T]GGAAAGACTAGAGGT | 10600 |
rs565957322 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29045013 | AGCTGTGTGTTATCA[A/G]ACTTCCAGATTTTGA | 10600 |
rs566030554 | snp | C/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29034341 | AGATGGAGTTTTTGC[C/T]CTTGTTGCCCAGGCT | 10600 |
rs566129539 | snp | A/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29037973 | GAAAGAAATATTGCT[A/G]CTTCTTTCATGGAGC | 10600 |
rs566386792 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29022642 | GGAAGCACGTGGTAC[A/G]ATGACCCTAAGGCTC | 10600 |
rs566495438 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29031802 | TATTATAGATCATGT[G/T]CAGATCTAACAGATA | 10600 |
rs566515904 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29031068 | TGAGGCAAGGAGCTA[C/G]ACCTTTCTACCTGTG | 10600 |
rs566557191 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29038657 | TTAAGCTTCCTTCTT[C/G]GGAATGTGTATATGT | 10600 |
rs566630123 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP16 | GRCh38.p7 | 21:29052968 | TCCAGCCTGGGTGAC[A/G]GAGTGAGACCCTGTC | 10600 |
rs566630602 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29032363 | CAGCCTCCTGAGTAG[A/C]TGGGACTACACCTGC | 10600 |
rs566742053 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29045968 | GCACCACCCATGTGT[A/G]CATTACAGGCACGCC | 10600 |
rs566798534 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29046499 | GGAACTTTTTAGGAT[C/T]AGATTGTGAGAGTGA | 10600 |
rs566930476 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29025820 | GTATTTCTTCAGGAC[C/T]TGCTATGTACTAACA | 10600 |
rs566979434 | snp | C/T | | | intron-variant, utr-variant-5-prime, upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29024956 | TGTCAGTTCCAGAAG[C/T]TGGCCAATGAGATGC | 10600 |
rs567094576 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29025261 | TTTCCACACGCTTAC[A/C]TTTTTAATGGAACCG | 10600 |
rs567237772 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29029706 | TTGTGTAACTCCATC[A/G]TCTGGGGAGACAGCA | 10600 |
rs567302766 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29036776 | GTTCTTTCCATGCAT[A/G]ATTAAATTAATTGGC | 10600 |
rs567344138 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP16 | GRCh38.p7 | 21:29050966 | GGCTGTTGTATTAAT[C/T]CAGCCAGTAGTTGAT | 10600 |
rs567363799 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29045240 | GTTCCCATCCTGTTT[C/G]CTGCCCTTCATTCTT | 10600 |
rs567457950 | snp | C/T | 0.0028556 | 0.0376782 | intron-variant | USP16 | GRCh38.p7 | 21:29053757 | CCCATGACATCTGTG[C/T]AAATGGAACTAGAAC | 10600 |
rs567530357 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29052209 | GCTGGCTGTTCATGG[A/G]CCACATTTTGAATAG | 10600 |
rs567596063 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29052925 | CAGGAGGCAGAGGTT[A/G]CATTGAGCTGAGATC | 10600 |
rs567744973 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29032204 | TGTAAATGGAGTCAT[A/G]CAGTGTGCAACATTT | 10600 |
rs567830331 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29024627 | TGGCCTAGCCACTTC[C/T]CATAATGCCGCGTTC | 10600 |
rs567887286 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29025185 | TATCCAATTGACTAT[A/G]TCTAGGAGGGGATTG | 10600 |
rs567893842 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | USP16 | GRCh38.p7 | 21:29031742 | CTGCGCCCAGCCAGG[A/C]TTTTTTGTTTTTTCA | 10600 |
rs568044347 | snp | C/T | 0.00119737 | 0.0244387 | downstream-variant-500B | USP16 | GRCh38.p7 | 21:29054718 | CCTAGGTTCACGCCA[C/T]TCTCCTGTCTCAGCC | 10600 |
rs568143352 | snp | A/G | 3.4293e-05 | 0.00414069 | missense | USP16 | GRCh38.p7 | 21:29046694 | CAACAAAAAATTCAA[A/G]GAAAAGTTCTTCATT | 10600 |
rs568263169 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29037791 | GGGTTTCGCCATGTT[A/G]CCTAGGCTAGTCTTG | 10600 |
rs568283061 | in-del | -/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29041786 | AAGGACTTTTTTGTC[-/T]TATTCATAAAAGGCG | 10600 |
rs568344609 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29026995 | TCAAGAGAGTGATAT[A/G]ATAAAAATGGCATAA | 10600 |
rs568371583 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP16 | GRCh38.p7 | 21:29041321 | GAATTACCCCTGCTG[A/G]CATTTTCTGTCAGAA | 10600 |
rs568896719 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29025346 | AGAACCGGCAAGACT[A/G]TCTTTGATTTAGATT | 10600 |
rs568905038 | in-del | -/TTT | | | downstream-variant-500B | USP16 | GRCh38.p7 | 21:29054628 | TTTTTTTTTTTTTTT[-/TTT]GAGACGGAGTCTTGC | 10600 |
rs568995434 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29046069 | CCTCAAGTGAGATGC[A/C]CTCCTTGGCCTCCCA | 10600 |
rs569010967 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29025944 | CCAGATTAAAGATTT[A/C]AGAAATTCACTAGAA | 10600 |
rs569149010 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29026953 | AGTTTAGGGAGTGTG[C/G]TCCAGGAAACTGTTA | 10600 |
rs569183419 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29040497 | ATTTTGGAATTATTT[A/C]GTAAATATGGGGAGC | 10600 |
rs569351519 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP16 | GRCh38.p7 | 21:29048231 | GGGACTACAGGCACC[C/T]GCCACCACACCTGGC | 10600 |
rs569605831 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | USP16 | GRCh38.p7 | 21:29028266 | TAGCTGGGATTACAG[A/T]CACATCCCACCACAG | 10600 |
rs569635756 | snp | A/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29050745 | GAGAGTTGAGAAATG[A/T]AGCCAGAGAAGTGAG | 10600 |
rs569663062 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29042255 | TTCTTTGTGGGAAAT[C/G]TCAGCACTCCTTAAA | 10600 |
rs569742972 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29034147 | CTTTGTTTTAGGAAC[A/G]CTAAACTGAAAGAAT | 10600 |
rs569769559 | in-del | -/G | 0.0162398 | 0.0886349 | intron-variant | USP16 | GRCh38.p7 | 21:29032596 | GTGTGTATCAAGTTT[-/G]CTCTTTTTTTATTAC | 10600 |
rs569799436 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29034648 | AATACTTGTTGACTT[A/C]AATGTTCTCAGTTGC | 10600 |
rs570121998 | snp | A/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29041130 | CTAGGCACGTGTGGC[A/G]CCTGAAATGTGACTG | 10600 |
rs570182412 | snp | G/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29036943 | GTCCATGTTCTTGAT[G/T]GTTTTATATTCTTAA | 10600 |
rs570215393 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29043805 | GTGCTTCTTTTTTTT[A/T]AAATCCTGCATTGCT | 10600 |
rs570263075 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29036129 | ATATGCATAGTCTTC[C/T]TCAGGAAAACAGAAT | 10600 |
rs570399715 | snp | A/G | 6.66989e-05 | 0.00577451 | missense | USP16 | GRCh38.p7 | 21:29047286 | GTGAAGTATGCACAC[A/G]GAGACAGTGTAATGG | 10600 |
rs570438913 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP16 | GRCh38.p7 | 21:29048119 | GACAGAGTCCTGCCC[C/T]TTCTCCCAGGCTAAA | 10600 |
rs570582944 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29041399 | CACGTATTTGGAAAA[C/T]TGGCTGATCAAGTAG | 10600 |
rs570627974 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29034054 | CTGGAGAGATATGTC[A/G]GGGTCAGAGGATGTC | 10600 |
rs570692278 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | USP16 | GRCh38.p7 | 21:29034533 | GGTCAGGCTGGTCTC[A/G]AACTCCTGACCTCAG | 10600 |
rs570762543 | snp | C/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29051638 | GAGTTCGAGACCAGC[C/T]TGGCCAGCATGGTGA | 10600 |
rs570763679 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29027134 | ATATAATTAGGTAGA[C/T]CTGTATGTACTTTTA | 10600 |
rs570875896 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29036038 | ACCAGTAAAGTAAAA[C/T]GTTTGGAGTATTTCA | 10600 |
rs570929623 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29050017 | ATTCTTTTGGACGTC[A/G]GAGGGGACTTCGGTT | 10600 |
rs571036214 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29049211 | GCATCTTGTTTTTAC[G/T]GACCCTTGATAAAAA | 10600 |
rs571319435 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29051631 | AGGTGAGGAGTTCGA[C/G]ACCAGCCTGGCCAGC | 10600 |
rs571505352 | snp | A/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29030088 | TCTGCTTGTGCTGCT[A/G]TACCATGTTTCGGAG | 10600 |
rs571525841 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29044603 | CAGGCATGTGCCACC[A/G]TACCTGGCTAACTTT | 10600 |
rs571632185 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | USP16 | GRCh38.p7 | 21:29050312 | CTTTGATCATTGTAC[C/T]TTTATAATTTGAAGA | 10600 |
rs571737662 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | USP16 | GRCh38.p7 | 21:29034212 | TGTTTAGGAGACTGT[A/T]AAGGAATCCAAACCA | 10600 |
rs571837133 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29051750 | GCAGGAGAATTGCTG[A/G]AACCTGGGAGGCAGA | 10600 |
rs571913612 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29027593 | CTGAGACTGTTCAAG[A/G]TCTGTGTAAGATGAC | 10600 |
rs572412079 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29050272 | TTAAGTATGAAGTTG[A/G]TAACACTTATTGAGT | 10600 |
rs572489889 | snp | C/T | 1.65836e-05 | 0.0028795 | intron-variant | USP16 | GRCh38.p7 | 21:29042549 | ACTATTGAATTTATT[C/T]TATTCAAGTAGATTT | 10600 |
rs572563605 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP16 | GRCh38.p7 | 21:29035574 | AGACGGGGTTTCACC[A/G]TGTTGGTCAGGCTGG | 10600 |
rs572569200 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29029286 | GGCGTGGTGGCGGGC[A/G]CCTGTAGTCCCAGCT | 10600 |
rs572583123 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29028850 | TAATCTTTAACTTTT[C/T]AGTATTATGAATGGC | 10600 |
rs572886657 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | USP16 | GRCh38.p7 | 21:29051326 | CATATCTGAGACCTA[C/T]AGCAGAGAGGTTAGG | 10600 |
rs572892339 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29051738 | CGGGAGGCTGAGGCA[A/G]GAGAATTGCTGGAAC | 10600 |
rs572918758 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29026698 | ACATCTGCCTTTTAG[C/T]TCATCGTTTGTGTGA | 10600 |
rs573158593 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29023772 | GACCGACTAATTTTT[G/T]GTATTTTTAGTAGAG | 10600 |
rs573262451 | snp | G/T | 0.000798403 | 0.0199641 | utr-variant-5-prime, upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29024716 | CACCAGGAGGAAGAC[G/T]GAGCTGGCTGCCCAG | 10600 |
rs573506602 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29051242 | ATAATGACTTCAGTT[C/T]TAGATACATTTGAGT | 10600 |
rs573518163 | snp | C/T | 0 | 0 | intron-variant | USP16 | GRCh38.p7 | 21:29053227 | AACATAAATAGTTGT[C/T]TGAAAAGTGGCTCCT | 10600 |
rs573802753 | snp | G/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29031329 | GTGGTACTAAAGTCA[G/T]GGTCTCTCAGTTACC | 10600 |
rs573847983 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29036484 | GAGTAACATTAGTTA[C/T]GGTTGATTGCAAACT | 10600 |
rs574011587 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29037224 | CCAAGTATACTTCTG[C/T]ATTCGATATGACTGT | 10600 |
rs574059730 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29031207 | GAGCTCTCAGCCGGC[C/T]ACATTCTCAGCACCT | 10600 |
rs574143135 | snp | A/C | | | intron-variant | USP16 | GRCh38.p7 | 21:29043011 | GGCAATTAAAGTCTC[A/C]CCAAATTTTATTTTC | 10600 |
rs574189024 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29022820 | TTGACTTGGGCCTTC[A/G]AACTTTGCACAGTAG | 10600 |
rs574329636 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29023624 | TTTCTTTTTGAGAGG[A/G]AGTTTTGCTCTTGTT | 10600 |
rs574454813 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29046200 | GAGTATAGTGTGCAT[A/G]ATCATACCTCACAGT | 10600 |
rs574491429 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | USP16 | GRCh38.p7 | 21:29045490 | TCAGGCCATTTTTTT[C/T]CCAGAATACTTTTGT | 10600 |
rs574516621 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | USP16 | GRCh38.p7 | 21:29032596 | GTGTGTATCAAGTTT[G/T]CTCTTTTTTTATTAC | 10600 |
rs574605111 | snp | A/T | | | upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29023261 | ACCCGGTCTCAATAA[A/T]TAAATAAATAAGTAA | 10600 |
rs574608117 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29031953 | TCCTGAGTTTGACTT[C/T]TTTTTTTGTGCATGT | 10600 |
rs574647872 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP16 | GRCh38.p7 | 21:29041028 | TTCTTATTATGTGGC[A/G]TGTAAAGATTTAGGG | 10600 |
rs574653206 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29025445 | AGTGTATTAAGTTTA[C/T]TGATGTTTTATAGCT | 10600 |
rs574705072 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP16 | GRCh38.p7 | 21:29047608 | TGACACATAGTGGCT[A/G]TTTTTTTCCACCCTT | 10600 |
rs574785103 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29041620 | ATCTTTTATCAGTCT[C/T]GAATGTTAGAATGTT | 10600 |
rs574909915 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | USP16 | GRCh38.p7 | 21:29054279 | TTAAAATCATGTTCA[C/T]TTAACATTAAATACA | 10600 |
rs574941360 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29047680 | GAACTAATATGACAT[A/G]CCCAGTGCAAAGCAC | 10600 |
rs575071083 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29031498 | GGCTGGAGTGCAGTG[A/G]CACAATCTTGGCTCA | 10600 |
rs575275324 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | USP16 | GRCh38.p7 | 21:29045367 | ATCTTGATGAAATGC[C/T]TTCTTTTCCTCTATT | 10600 |
rs575281375 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29024760 | GAGGGGATGCAGTTA[C/T]GGGCTCTGTCGCCGT | 10600 |
rs575549987 | in-del | -/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29034303 | GAGTGCATGGTTTTC[-/T]TTTTTTTTTTTTTTT | 10600 |
rs575683871 | in-del | -/A | | | intron-variant | USP16 | GRCh38.p7 | 21:29048440 | GTGATGGAATATACT[-/A]AACTTTCAACCTCAT | 10600 |
rs575701834 | snp | A/C | | | intron-variant | USP16 | GRCh38.p7 | 21:29052327 | ACTGGGCAATTTACA[A/C]AAGAAAGAGGTTTAC | 10600 |
rs575892183 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29040056 | AATGAGTACTAATAA[C/T]AGTGATAATAACTAA | 10600 |
rs575973415 | snp | A/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29034239 | ACCAGACTTGACTGC[A/G]TTAGTGTGGTTTAAT | 10600 |
rs575988021 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP16 | GRCh38.p7 | 21:29040940 | TTAAAATTATAATTA[A/G]CAGTAATACATGAAT | 10600 |
rs576472009 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29049422 | ATTCACTAAGCTTGG[C/T]TTGAGCATGAGGCTG | 10600 |
rs576508294 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29048542 | TATTTTGATTTCATC[A/T]GTAAGAATTTATGGA | 10600 |
rs576531369 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP16 | GRCh38.p7 | 21:29028224 | CCTCCCAGGTTCAAA[C/T]GGTTCTCTCGTGCCT | 10600 |
rs576550620 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | USP16 | GRCh38.p7 | 21:29035459 | GCTCACCACAACCTC[C/T]GCCTCCCAGGTTCAA | 10600 |
rs576682664 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29028788 | AAAGACCATGGATGT[A/G]TATTTCATAATTTAT | 10600 |
rs576743862 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP16 | GRCh38.p7 | 21:29042941 | GATGTTATGAGTATT[C/G]GATAAATCATTCTTC | 10600 |
rs576860636 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29039678 | TATTAAGGCCATCAT[A/C]CTTTAAAATTTTTTC | 10600 |
rs576928428 | snp | C/T | 1.68122e-05 | 0.00289928 | intron-variant | USP16 | GRCh38.p7 | 21:29039012 | AAGAAAGTAATTTCT[C/T]TTCCCATATTCAGGA | 10600 |
rs576975976 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29034349 | TTTTTGCTCTTGTTG[C/T]CCAGGCTAGAGTGCA | 10600 |
rs577003138 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP16 | GRCh38.p7 | 21:29032615 | TTTTTTTATTACTGA[A/G]CGTATTTTATGGCAT | 10600 |
rs577077178 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29026198 | GTGCTGTGGCTCACG[C/G]CTGTAATCCCAGCAC | 10600 |
rs577110683 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29027687 | CTATGCTATGAAAAA[C/T]GGGAGATAACTATTC | 10600 |
rs577319467 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29042364 | TTCTTAAGCCTTTGT[G/T]TATTTTAAAACCCAT | 10600 |
rs577379454 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29041681 | TCAGCCTACTCTGAG[C/T]TGTTCATTTTATACT | 10600 |
rs577492105 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29051163 | CACGACAGATGGGAG[G/T]GCTGTAAATTGAGAT | 10600 |
rs577998887 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP16 | GRCh38.p7 | 21:29043912 | ATATAAAGGTAAACA[A/G]TAAGTCCCCCTCCCA | 10600 |
rs578009854 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29027635 | CCTGACCTTTACATA[C/T]ATTGAAAACCTCTTA | 10600 |
rs578153582 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | USP16 | GRCh38.p7 | 21:29029361 | GAGCTTGCAGTGAGC[C/G/T]GAGATTGTGCCACTG | 10600 |
rs578252032 | snp | A/T | | | missense | USP16 | GRCh38.p7 | 21:29043472 | AAAAGACAGTGGAGG[A/T]TGAAGATCAAGATAG | 10600 |
rs745319324 | snp | C/T | 0.000349071 | 0.0132066 | intron-variant | USP16 | GRCh38.p7 | 21:29040560 | TATTTCTAAGGAAAA[C/T]AAAATTTAAAATTTA | 10600 |
rs745345757 | snp | A/G | 1.95612e-05 | 0.00312734 | intron-variant | USP16 | GRCh38.p7 | 21:29030547 | AGATTAACTGAAGAA[A/G]GTCATTTTTGACCTT | 10600 |
rs745362586 | snp | C/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29046028 | GGGTTTTCACCATGT[C/T]GGCCAGGCTGGTTTC | 10600 |
rs745413044 | snp | A/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29053340 | GGAAAGTGAACACTT[A/G]AGAGGTTGAATGTGC | 10600 |
rs745429650 | snp | A/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29048257 | CTGGCTAATTTTTGT[A/G]TTTTTAATAGAGATA | 10600 |
rs745452894 | snp | A/G | | | utr-variant-3-prime | USP16 | GRCh38.p7 | 21:29054460 | GGGTGATGGATCACA[A/G]CACATCAATAAACTG | 10600 |
rs745516667 | snp | A/G | 1.66629e-05 | 0.00288638 | splice-donor-variant | USP16 | GRCh38.p7 | 21:29039569 | GCAGAAGAACACCAA[A/G]TTAGCATGTTATGAC | 10600 |
rs745549195 | snp | A/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29040950 | AATTAGCAGTAATAC[A/G]TGAATTATATTTGTT | 10600 |
rs745599001 | in-del | -/AGG | 5.23921e-05 | 0.00511794 | intron-variant | USP16 | GRCh38.p7 | 21:29043610 | CCAAGGTGGGTAATT[-/AGG]AGGAAAATCATATGC | 10600 |
rs745633335 | snp | A/C | 3.35497e-05 | 0.00409558 | missense | USP16 | GRCh38.p7 | 21:29043475 | AGACAGTGGAGGATG[A/C]AGATCAAGATAGTGA | 10600 |
rs745687246 | in-del | -/TT | 1.65509e-05 | 0.00287666 | frameshift-variant | USP16 | GRCh38.p7 | 21:29050119 | TACGCAAAGTTAACA[-/TT]AACACATAAAGTTTC | 10600 |
rs745695690 | snp | G/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29045993 | CACGCCTGGCTAATT[G/T]TTGTATTTTTAGTAG | 10600 |
rs745737179 | snp | A/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29031330 | TGGTACTAAAGTCAG[A/G]GTCTCTCAGTTACCC | 10600 |
rs745767880 | snp | C/G | 0.000139577 | 0.00835279 | intron-variant | USP16 | GRCh38.p7 | 21:29043377 | TTTTTTCACCAAATG[C/G]TAGTTGTAAAATTTT | 10600 |
rs745794440 | snp | C/T | 3.29669e-05 | 0.00405984 | synonymous-codon, utr-variant-5-prime | USP16 | GRCh38.p7 | 21:29030683 | GAATATCTGCCAAGA[C/T]TGTAAGACTGACAAT | 10600 |
rs745888902 | snp | A/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29032308 | ATAATCACGGCTCAC[A/G]GCAGCCTTCACCTCC | 10600 |
rs745966848 | in-del | -/T | 1.64879e-05 | 0.00287118 | intron-variant | USP16 | GRCh38.p7 | 21:29034827 | GGTTTATGATTATGA[-/T]TTTTTTTAGGGCTGT | 10600 |
rs746096046 | snp | C/G | 1.64946e-05 | 0.00287176 | missense, utr-variant-5-prime | USP16 | GRCh38.p7 | 21:29038368 | GTGCTTAGAGAACTA[C/G]TAAAAGAAGTGAAAA | 10600 |
rs746106060 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29027206 | AGTGAAGATTTGATG[C/T]GCAGCTAGATTTGTC | 10600 |
rs746140386 | snp | C/T | 1.65119e-05 | 0.00287327 | missense | USP16 | GRCh38.p7 | 21:29054156 | TACTAAACTCACAAG[C/T]GTACCTCCTATTTTA | 10600 |
rs746175862 | snp | C/T | 3.42765e-05 | 0.0041397 | intron-variant | USP16 | GRCh38.p7 | 21:29053752 | TCTTGCCCATGACAT[C/T]TGTGTAAATGGAACT | 10600 |
rs746180862 | snp | A/G | 1.64822e-05 | 0.00287068 | synonymous-codon, utr-variant-5-prime | USP16 | GRCh38.p7 | 21:29036292 | CGTATGTGATAATGA[A/G]GTCCAGTATTGTAGT | 10600 |
rs746225097 | snp | A/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29049116 | CTTACTTTTATTTCA[A/G]GTTAAAAAAAGAAAA | 10600 |
rs746340997 | snp | C/T | 3.364e-05 | 0.00410108 | missense | USP16 | GRCh38.p7 | 21:29042043 | AATCAATGCCAAGTT[C/T]TGTTGACCGCATCTT | 10600 |
rs746375177 | snp | A/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29050505 | ACATAGGTCAGGAGT[A/G]GTATACACTTAACCC | 10600 |
rs746428836 | snp | C/T | 3.29663e-05 | 0.00405981 | synonymous-codon | USP16 | GRCh38.p7 | 21:29047140 | GTATGAGGTTGTAAA[C/T]GAAGATCCAGAAACT | 10600 |
rs746430902 | snp | A/G | 1.96566e-05 | 0.00313495 | intron-variant | USP16 | GRCh38.p7 | 21:29040726 | AAACACTATAGTTGA[A/G]TTCCTCTGTACCTTA | 10600 |
rs746467586 | snp | C/G | 1.7307e-05 | 0.00294163 | intron-variant | USP16 | GRCh38.p7 | 21:29050048 | TACTTAACCTGTATT[C/G]CTTTTCCAAGAAAAG | 10600 |
rs746477120 | snp | C/T | 1.64751e-05 | 0.00287007 | stop-gained, utr-variant-5-prime | USP16 | GRCh38.p7 | 21:29034855 | TGTGGCAGAAATTCT[C/T]AGGAGCAGCATGCCT | 10600 |
rs746493363 | snp | C/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29030592 | TATTATTTGTTTTAA[C/T]AGAACCTGTGTGCAG | 10600 |
rs746630414 | snp | A/G | 1.82998e-05 | 0.00302482 | intron-variant | USP16 | GRCh38.p7 | 21:29040693 | AAAGTTAAAGGTAAT[A/G]TCTGACTTTTTGAAC | 10600 |
rs746702838 | snp | A/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29036932 | ATTTATTTCATGTCC[A/G]TGTTCTTGATTGTTT | 10600 |
rs746722468 | snp | C/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29040579 | ATTTAAAATTTAATA[C/G]TATATATATATCCAT | 10600 |
rs746765985 | snp | A/G | 1.65345e-05 | 0.00287524 | missense, utr-variant-5-prime | USP16 | GRCh38.p7 | 21:29039042 | AACCATTAGAAATAA[A/G]CCTTGAGCCTCCAGG | 10600 |
rs746851590 | snp | A/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29042932 | AAAAGAAGAGATGTT[A/G]TGAGTATTGGATAAA | 10600 |
rs746885365 | snp | A/G | 1.64917e-05 | 0.00287151 | synonymous-codon, utr-variant-5-prime | USP16 | GRCh38.p7 | 21:29038379 | ACTACTAAAAGAAGT[A/G]AAAATGTCTGGAACA | 10600 |
rs746929707 | snp | A/C | 1.7663e-05 | 0.00297173 | intron-variant | USP16 | GRCh38.p7 | 21:29043616 | TGGGTAATTAGGAGG[A/C]AAATCATATGCTTGT | 10600 |
rs747016127 | snp | C/T | 5.03385e-05 | 0.00501665 | synonymous-codon | USP16 | GRCh38.p7 | 21:29042053 | AAGTTTTGTTGACCG[C/T]ATCTTTGGTGGTGAA | 10600 |
rs747106668 | snp | C/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29050282 | AGTTGATAACACTTA[C/T]TGAGTAGAGTGGGTC | 10600 |
rs747112618 | in-del | -/AA | | | intron-variant | USP16 | GRCh38.p7 | 21:29053663 | AGAAGAGGTATGGAG[-/AA]AAGAGTAGACTCATG | 10600 |
rs747173602 | snp | A/G | 1.64817e-05 | 0.00287064 | synonymous-codon | USP16 | GRCh38.p7 | 21:29047173 | TTTCTGTACTCTTGC[A/G]AACAGGGAAGTTTTC | 10600 |
rs747183984 | snp | A/G | 8.50854e-05 | 0.00652192 | utr-variant-5-prime, upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29027890 | TGTTATTTTGTGTCA[A/G]TAAGTAATCCATAAA | 10600 |
rs747185503 | snp | A/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29035222 | GATAGGGACGCTAAG[A/G]ACAAATTTCAGATAA | 10600 |
rs747236473 | in-del | -/TGTA | | | intron-variant | USP16 | GRCh38.p7 | 21:29047920 | AAGCCTGTGTGTGTG[-/TGTA]TGTATCTTATATGTG | 10600 |
rs747254889 | snp | A/G | 0.000251477 | 0.0112105 | upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29024591 | AGCCGATGGTCCCGG[A/G]AGGTGGGGGTGGGGT | 10600 |
rs747308739 | snp | C/T | 3.29603e-05 | 0.00405944 | intron-variant | USP16 | GRCh38.p7 | 21:29054022 | AAAAAGTAATCAACT[C/T]GAATCTTTCCATTTA | 10600 |
rs747396801 | snp | C/T | 1.64741e-05 | 0.00286998 | missense | USP16 | GRCh38.p7 | 21:29053908 | ATGCCAAGGCAAGAA[C/T]CGCAAATAGTCATCT | 10600 |
rs747399617 | snp | C/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29025607 | TTTCAAGTTTTCCTA[C/T]GGAGTCTAAGCTGCT | 10600 |
rs747435848 | in-del | -/C | | | intron-variant, upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29026071 | CCTTGAAATGGAGAG[-/C]TTCCAAGATTGGTAA | 10600 |
rs747487872 | snp | C/T | 1.65318e-05 | 0.002875 | intron-variant | USP16 | GRCh38.p7 | 21:29037244 | GATATGACTGTATTA[C/T]ACATTTTGCTAAATC | 10600 |
rs747547318 | snp | C/T | 1.64765e-05 | 0.00287019 | synonymous-codon | USP16 | GRCh38.p7 | 21:29053858 | TGGAGTTGTTGAACA[C/T]AGTGGTACTATGAGG | 10600 |
rs747558289 | snp | C/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29048692 | TTTGGAATGATTTTA[C/T]AGCAAATCTGAATGC | 10600 |
rs747577870 | snp | A/G | 1.6477e-05 | 0.00287024 | missense, utr-variant-5-prime | USP16 | GRCh38.p7 | 21:29036320 | AGTTCAAACCAGTTG[A/G]GTCAAGTGGTTGATT | 10600 |
rs747613750 | snp | A/G | 5.50312e-05 | 0.00524524 | intron-variant | USP16 | GRCh38.p7 | 21:29042137 | ATACTGGGTTTATTT[A/G]CTAATATTCAACAGT | 10600 |
rs747680410 | snp | A/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29043862 | ATTAACTTAATTTTC[A/G]AGTTAATATTATTGA | 10600 |
rs747684451 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29027261 | GCAATAATATAATAA[C/T]GTAAATAGTTGAGAA | 10600 |
rs747717550 | snp | C/T | 1.78992e-05 | 0.00299153 | intron-variant | USP16 | GRCh38.p7 | 21:29050223 | TCCTTTAAAGTCAAA[C/T]TGTGGCTTACCTAAT | 10600 |
rs747733778 | snp | C/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29028839 | ACAGATTTAGGTAAT[C/G]TTTAACTTTTTAGTA | 10600 |
rs747776533 | in-del | -/T | 0.000656599 | 0.0181071 | intron-variant, upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29027834 | AAATATAAGACATAC[-/T]TTTTTTTTTGGTCAA | 10600 |
rs747800328 | snp | C/T | 1.6857e-05 | 0.00290314 | intron-variant | USP16 | GRCh38.p7 | 21:29050078 | GAAGTCAATCTGTTA[C/T]GCTTCTCTTTTAGGC | 10600 |
rs747808775 | snp | A/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29050655 | AGGAGTAAAAACAGC[A/G]GTGTAAAATAGGATG | 10600 |
rs747823878 | snp | A/G | 1.65326e-05 | 0.00287507 | intron-variant | USP16 | GRCh38.p7 | 21:29036263 | CATCTCTGATTTTTG[A/G]GTCACAGGTGTTACG | 10600 |
rs747897321 | snp | A/G | 9.89006e-05 | 0.00703139 | missense | USP16 | GRCh38.p7 | 21:29047189 | AACAGGGAAGTTTTC[A/G]ATACTGATGAGTGTT | 10600 |
rs747934657 | snp | A/G | 1.66957e-05 | 0.00288922 | missense, upstream-variant-2KB, utr-variant-5-prime | USP16 | GRCh38.p7 | 21:29027918 | AAAGTGCCAACATGG[A/G]AAAGAAACGGACAAA | 10600 |
rs748055934 | snp | A/G | 1.66615e-05 | 0.00288626 | intron-variant | USP16 | GRCh38.p7 | 21:29039187 | GATTGTGCTTTCAGT[A/G]CCTCAGTGAGATGCT | 10600 |
rs748126101 | snp | C/T | 1.96949e-05 | 0.00313801 | intron-variant | USP16 | GRCh38.p7 | 21:29037268 | CTAAATCTTTTCTTT[C/T]TTTAAAGCAGAGAAA | 10600 |
rs748138797 | snp | A/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29042776 | ATTGGTTTCCATACA[A/G]TGAAGTATTTTCCTT | 10600 |
rs748148232 | snp | C/T | 3.30011e-05 | 0.00406195 | synonymous-codon, utr-variant-5-prime | USP16 | GRCh38.p7 | 21:29039058 | CCTTGAGCCTCCAGG[C/T]CCTCTTACTTTAGCC | 10600 |
rs748183411 | in-del | -/TA | | | intron-variant | USP16 | GRCh38.p7 | 21:29047971 | ATATGTGTGTGTATG[-/TA]TATATATATAAGCTC | 10600 |
rs748205755 | snp | A/G | | | missense | USP16 | GRCh38.p7 | 21:29047250 | GTAATGAGAAACTTC[A/G]AGATGCGAATAAACT | 10600 |
rs748216773 | in-del | -/GTT | | | intron-variant | USP16 | GRCh38.p7 | 21:29053471 | AACAGGGTATTCAGA[-/GTT]GTTAATAGCTAGGGT | 10600 |
rs748219197 | snp | C/T | 1.65471e-05 | 0.00287633 | intron-variant | USP16 | GRCh38.p7 | 21:29042538 | GATCAGGTAAGACTA[C/T]TGAATTTATTTTATT | 10600 |
rs748259038 | snp | C/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29032972 | TTTTATTTTAGCCAT[C/G]ATGATAGTTATATAC | 10600 |
rs748297889 | snp | C/T | 1.90623e-05 | 0.0030872 | intron-variant | USP16 | GRCh38.p7 | 21:29042149 | TTTGCTAATATTCAA[C/T]AGTTTATCAATTGTT | 10600 |
rs748334376 | snp | A/C | 5.61698e-05 | 0.00529922 | intron-variant | USP16 | GRCh38.p7 | 21:29028006 | GAATCTTTAATGTTT[A/C]TATCTCTAAATGAAT | 10600 |
rs748339873 | snp | G/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29048295 | GCCACGTTGGCCAGG[G/T]TGGTCTCAAACTCCT | 10600 |
rs748351658 | in-del | -/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29037877 | GGCGTGAGCCACCAT[-/G]GCCTGGCCAAAGAAA | 10600 |
rs748366395 | in-del | -/AGTG | 1.67069e-05 | 0.00289019 | frameshift-variant | USP16 | GRCh38.p7 | 21:29043486 | GATGAAGATCAAGAT[-/AGTG]AGGAAGAAAAAGATA | 10600 |
rs748373501 | in-del | -/T | 1.65149e-05 | 0.00287353 | frameshift-variant | USP16 | GRCh38.p7 | 21:29048806 | AAAAGCAGATGCTAA[-/T]TTCTCTTGCTCCTCC | 10600 |
rs748397832 | snp | C/G | 1.65395e-05 | 0.00287567 | missense | USP16 | GRCh38.p7 | 21:29046933 | TATGAAAAATATCAA[C/G]ATGGATAATGATCTG | 10600 |
rs748487844 | snp | A/G | 4.94576e-05 | 0.00497256 | missense | USP16 | GRCh38.p7 | 21:29054137 | GCTGTGCCTACAACT[A/G]AAGTACTAAACTCAC | 10600 |
rs748572563 | snp | A/G | 1.65097e-05 | 0.00287308 | missense | USP16 | GRCh38.p7 | 21:29046857 | ACCAGAAAGATTTGA[A/G]TGGCCAAGCAAAAAT | 10600 |
rs748619769 | snp | C/T | | | upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29023885 | ATTACAGGGGTGAGC[C/T]ACCGCGCCAGGGCTC | 10600 |
rs748659268 | snp | A/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29025474 | CTGATGGAAGTCACA[A/G]TATGCTCTCCTCATG | 10600 |
rs748688483 | snp | C/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29046601 | CTTCTTCCTCTATCT[C/G]TCTTCCTCCTTTTCT | 10600 |
rs748693188 | snp | C/T | 1.65121e-05 | 0.00287329 | synonymous-codon, utr-variant-5-prime | USP16 | GRCh38.p7 | 21:29037421 | AACCGTGAAAGGACT[C/T]AGTAATTTGGGAAAC | 10600 |
rs748706340 | snp | C/G | 1.65192e-05 | 0.00287391 | missense | USP16 | GRCh38.p7 | 21:29046808 | TCCAACCATATTTCA[C/G]AAGAGGGTGTTATGC | 10600 |
rs748732278 | snp | C/T | 4.94393e-05 | 0.00497164 | intron-variant | USP16 | GRCh38.p7 | 21:29054038 | GAATCTTTCCATTTA[C/T]GTTTGATTTTTCATT | 10600 |
rs748865024 | snp | A/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29041114 | TTCCATATAGAAGCA[A/G]CTAGGCACGTGTGGC | 10600 |
rs748916005 | snp | C/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29025855 | GCTAGATATTATAGG[C/G]AGTTCCAAAACTGTG | 10600 |
rs748962067 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29026962 | AGTGTGGTCCAGGAA[A/G]CTGTTAAATGCTTCC | 10600 |
rs749015487 | snp | A/G | 3.29484e-05 | 0.00405871 | synonymous-codon | USP16 | GRCh38.p7 | 21:29053876 | TGGTACTATGAGGTC[A/G]GGGCATTACACTGCC | 10600 |
rs749042910 | snp | G/T | 1.65493e-05 | 0.00287652 | missense | USP16 | GRCh38.p7 | 21:29048771 | TTTAGGTGAAAGGAA[G/T]CATGTTTACACCAAT | 10600 |
rs749061953 | snp | C/G/T | 6.87597e-05 | 0.00586309 | missense | USP16 | GRCh38.p7 | 21:29047310 | GTAATGGACCAAAGG[C/G/T]AAATATAAAAGGTAT | 10600 |
rs749129880 | snp | A/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29037183 | AGAATGACTTCAGGT[A/G]AACTCACAAACTCTA | 10600 |
rs749208098 | in-del | -/T | 3.29614e-05 | 0.00405951 | intron-variant | USP16 | GRCh38.p7 | 21:29054028 | TAATCAACTTGAATC[-/T]TTCCATTTATGTTTG | 10600 |
rs749213920 | snp | A/C | 2.0562e-05 | 0.00320633 | intron-variant | USP16 | GRCh38.p7 | 21:29028019 | TTATATCTCTAAATG[A/C]ATATGTTTTAAAATG | 10600 |
rs749228284 | snp | A/T | 1.6684e-05 | 0.00288821 | missense, upstream-variant-2KB, utr-variant-5-prime | USP16 | GRCh38.p7 | 21:29027941 | CGGACAAAGGGAAAA[A/T]CTGTTCCAATCGATG | 10600 |
rs749234984 | snp | A/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29053464 | TTTTTTAAACAGGGT[A/G]TTCAGAGTTGTTAAT | 10600 |
rs749287979 | snp | C/T | | | downstream-variant-500B | USP16 | GRCh38.p7 | 21:29054760 | TGGGACTACAGGCGC[C/T]CGCCACCACGCCCAG | 10600 |
rs749309927 | snp | A/G | 1.64914e-05 | 0.00287149 | synonymous-codon | USP16 | GRCh38.p7 | 21:29054145 | TACAACTAAAGTACT[A/G]AACTCACAAGCGTAC | 10600 |
rs749355974 | snp | A/G | | | upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29023510 | ACGGTAGCGATTACT[A/G]TCTTCTCTACTAAAC | 10600 |
rs749378815 | in-del | -/TGGTAG | 2.32167e-05 | 0.00340702 | intron-variant | USP16 | GRCh38.p7 | 21:29043375 | TTTTTTTTCACCAAA[-/TGGTAG]TTGTAAAATTTTGTT | 10600 |
rs749482786 | snp | A/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29030221 | CACAGTGCCTGCCCT[A/G]TAGTAGGTGTATTAT | 10600 |
rs749488946 | snp | A/T | 6.92641e-05 | 0.00588449 | missense | USP16 | GRCh38.p7 | 21:29043450 | AGTGTAAATGATAAA[A/T]ATCTGAAAAAGACAG | 10600 |
rs749499143 | snp | A/G | 3.43477e-05 | 0.00414399 | intron-variant | USP16 | GRCh38.p7 | 21:29037468 | CAGTTATGCAGGTAC[A/G]TTGTCATTTTTTTCC | 10600 |
rs749571941 | in-del | -/A | | | intron-variant, upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29026457 | CAAGACTCCGTCTCA[-/A]AAAAAAAAAAAAAAA | 10600 |
rs749572983 | in-del | -/T | 1.6707e-05 | 0.0028902 | intron-variant | USP16 | GRCh38.p7 | 21:29039019 | TAATTTCTTTTCCCA[-/T]ATTCAGGAACCATTA | 10600 |
rs749576083 | snp | A/G | 3.84512e-05 | 0.00438453 | intron-variant | USP16 | GRCh38.p7 | 21:29040718 | TTGAACTAAAACACT[A/G]TAGTTGAATTCCTCT | 10600 |
rs749578873 | snp | A/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29042561 | ATTTTATTCAAGTAG[A/T]TTTTTTTTCCTGTAA | 10600 |
rs749707178 | snp | A/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29049288 | CTGGAAAACTTTTGC[A/T]ATAGCTGTATAACTT | 10600 |
rs749798769 | in-del | -/TTTTTTTTT | | | downstream-variant-500B | USP16 | GRCh38.p7 | 21:29054601 | TTACAAGTGTGTTAA[-/TTTTTTTTT]TTTTTTTTTTTTTTT | 10600 |
rs749872857 | snp | A/G | 4.96339e-05 | 0.00498142 | synonymous-codon | USP16 | GRCh38.p7 | 21:29046951 | GGATAATGATCTGGA[A/G]GTTTTAACATCTTCT | 10600 |
rs750022907 | snp | A/T | 1.66327e-05 | 0.00288376 | utr-variant-3-prime | USP16 | GRCh38.p7 | 21:29054193 | AATACTGTAATAATA[A/T]CAAAAGCACTTTTTC | 10600 |
rs750072637 | in-del | -/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29025885 | GCTTGAAACCATTTA[-/T]TTTTCTAAGAACTTT | 10600 |
rs750088290 | snp | C/T | 1.69645e-05 | 0.00291238 | intron-variant | USP16 | GRCh38.p7 | 21:29038313 | AATAATTTTTCTCTT[C/T]TTTTTTCACCCTACA | 10600 |
rs750142940 | snp | C/T | 5.05438e-05 | 0.00502686 | intron-variant | USP16 | GRCh38.p7 | 21:29050185 | AAATGTAAGGTAAGT[C/T]AAAGTGGTCTTTTTC | 10600 |
rs750158908 | snp | C/T | 1.64808e-05 | 0.00287057 | missense | USP16 | GRCh38.p7 | 21:29054123 | ACACACATGTGCAAG[C/T]TGTGCCTACAACTAA | 10600 |
rs750222548 | snp | C/T | 4.95119e-05 | 0.00497529 | intron-variant | USP16 | GRCh38.p7 | 21:29034961 | TTTCAGTTCCTCTGC[C/T]TCTTGGGTGGAAATT | 10600 |
rs750255353 | in-del | -/TA | | | intron-variant | USP16 | GRCh38.p7 | 21:29052256 | ATATGGGAATTATAT[-/TA]TGTCAGTTTCCATGC | 10600 |
rs750309340 | snp | A/G | | | upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29022918 | ACCAAACAAGGACCA[A/G]CCCAATATCTCTTGG | 10600 |
rs750357038 | snp | G/T | 1.64982e-05 | 0.00287208 | intron-variant | USP16 | GRCh38.p7 | 21:29034817 | TATGGCTTTGAGGTT[G/T]ATGATTATGATTTTT | 10600 |
rs750387241 | snp | C/T | 3.50496e-05 | 0.00418612 | missense | USP16 | GRCh38.p7 | 21:29040670 | AGTTGGATGAAGAAC[C/T]AAAAAATAAAGTTAA | 10600 |
rs750403472 | snp | A/G | 1.65072e-05 | 0.00287286 | missense | USP16 | GRCh38.p7 | 21:29047084 | CCTGATGAAATAAAT[A/G]TAGAGATTCTGAATG | 10600 |
rs750431552 | snp | C/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29047765 | GACAATTTCCCTTAT[C/T]TCCCCATTGCTTTTT | 10600 |
rs750472555 | snp | A/G | 1.65282e-05 | 0.00287469 | missense, splice-donor-variant | USP16 | GRCh38.p7 | 21:29039146 | GAACTCTTTTCTCAG[A/G]TCTGTAAAAAGTGAG | 10600 |
rs750542233 | snp | C/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29052769 | AATAAGATTTATGTC[C/T]CTTCAGCTCAGGAGT | 10600 |
rs750620671 | snp | C/T | 5.21191e-05 | 0.00510459 | intron-variant | USP16 | GRCh38.p7 | 21:29043605 | GCAAGCCAAGGTGGG[C/T]AATTAGGAGGAAAAT | 10600 |
rs750704513 | snp | C/T | 1.66438e-05 | 0.00288472 | missense | USP16 | GRCh38.p7 | 21:29053806 | CATTTTTAAAGAATG[C/T]TGCAGAAGAAAATAC | 10600 |
rs750733363 | snp | A/G | 5.24398e-05 | 0.00512027 | intron-variant | USP16 | GRCh38.p7 | 21:29042111 | TGCAGAACTGTAAGT[A/G]GATGTCATGTATACT | 10600 |
rs750734088 | snp | A/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29044813 | TGTTATGGATGTGCC[A/G]TAATTCATTTAACCA | 10600 |
rs750734461 | snp | C/T | | | stop-gained, utr-variant-5-prime | USP16 | GRCh38.p7 | 21:29039518 | CAGCAGCAAGACAGC[C/T]AGGAGCTGCTTCGCT | 10600 |
rs750734600 | snp | A/C | | | upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29023220 | GAGGTCGTGCCACTG[A/C]ACTCCAGCCTGGGTA | 10600 |
rs750815501 | in-del | -/TTCCAA | 1.65405e-05 | 0.00287576 | cds-indel | USP16 | GRCh38.p7 | 21:29047026 | TGGAGAAGTGGACAT[-/TTCCAA]TGGTTTCAAAAACCT | 10600 |
rs750856755 | snp | C/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29029872 | ATGTGGGTACTAAAT[C/G]TTAGTTTTCTCATTT | 10600 |
rs750903980 | snp | A/C/T | 8.28733e-05 | 0.00643666 | synonymous-codon, missense, utr-variant-5-prime | USP16 | GRCh38.p7 | 21:29039488 | TTCTCTAGAGCAGTG[A/C/T]GGTTTAAAGGCTATC | 10600 |
rs750961394 | in-del | -/T | 1.65446e-05 | 0.00287612 | intron-variant | USP16 | GRCh38.p7 | 21:29042455 | CATTTTTACACTGTC[-/T]TTTCTGATTGGTTAA | 10600 |
rs750978803 | snp | C/G | 1.84834e-05 | 0.00303996 | intron-variant, upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29027864 | AGCTAACTTTATCTT[C/G]TTTTCTAGATTGTTA | 10600 |
rs751066152 | snp | C/T | 1.8144e-05 | 0.00301193 | intron-variant | USP16 | GRCh38.p7 | 21:29042005 | GATAGACTTTTTTTT[C/T]TCCATAGATTATGAG | 10600 |
rs751143299 | snp | A/G | 3.30044e-05 | 0.00406216 | missense | USP16 | GRCh38.p7 | 21:29047100 | TAGAGATTCTGAATG[A/G]TAGTCATACTCCTGG | 10600 |
rs751175475 | in-del | -/GGTAATTATATAAAC | 4.29433e-05 | 0.00463355 | intron-variant | USP16 | GRCh38.p7 | 21:29041982 | TATATAACGGTAATT[-/GGTAATTATATAAAC]GGTAATTGATAGACT | 10600 |
rs751284093 | snp | A/G | 4.9652e-05 | 0.00498232 | missense | USP16 | GRCh38.p7 | 21:29047003 | GCCTACCTAACGGAA[A/G]GGAGCAATGGAGAAG | 10600 |
rs751286101 | snp | A/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29033456 | CGGCAATGGAAACAC[A/G]ACCGGTTGTTGTACT | 10600 |
rs751381174 | snp | A/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29037923 | TATTGCATGACAGTA[A/G]GAGAGTTTGGTGAGC | 10600 |
rs751479936 | snp | C/T | 3.29864e-05 | 0.00406105 | missense | USP16 | GRCh38.p7 | 21:29053832 | AATACAAGGGTACTC[C/T]ATTCCTTATATGGAG | 10600 |
rs751538712 | snp | A/G | 1.67326e-05 | 0.00289241 | intron-variant | USP16 | GRCh38.p7 | 21:29036378 | CTCCAAAGCCAGGTA[A/G]AATAATTTGTTTCTT | 10600 |
rs751546795 | snp | A/G | 1.70458e-05 | 0.00291935 | synonymous-codon | USP16 | GRCh38.p7 | 21:29042095 | GATCATGTGTGATCA[A/G]TGCAGAACTGTAAGT | 10600 |
rs751556623 | snp | G/T | 1.68122e-05 | 0.00289928 | intron-variant | USP16 | GRCh38.p7 | 21:29036231 | TCCCCCTTTTTAGTT[G/T]TCATTTTGTCATTTT | 10600 |
rs751580803 | snp | C/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29045810 | CATTTAAATAACTTT[C/T]TCTTTCTTTTTTTTG | 10600 |
rs751775935 | snp | A/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29051066 | TAATGATTGATTGGC[A/T]CTGTAAGGTGAGGCA | 10600 |
rs751795199 | snp | A/T | 1.65564e-05 | 0.00287714 | synonymous-codon | USP16 | GRCh38.p7 | 21:29046771 | AGCTGAAATGTCACT[A/T]CAAGGAGAAGTAAAT | 10600 |
rs751874135 | in-del | -/T | 1.64946e-05 | 0.00287176 | frameshift-variant, utr-variant-5-prime | USP16 | GRCh38.p7 | 21:29038368 | TGCTTAGAGAACTAC[-/T]TAAAAGAAGTGAAAA | 10600 |
rs751898444 | snp | A/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29052422 | TACATGGATGGCAGC[A/G]GGCAAAGCAAGAGCT | 10600 |
rs751900105 | snp | C/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29036447 | CTTAGATTTGTTATA[C/T]TACCTAGCATTACAT | 10600 |
rs751905714 | snp | A/T | 2.00979e-05 | 0.00316994 | intron-variant | USP16 | GRCh38.p7 | 21:29043414 | GACCTATGTTATCTA[A/T]ATTTTAAGAGTGGTA | 10600 |
rs751945562 | snp | A/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29043219 | CCTTTTGCTGTTTTG[A/T]TGGTTTGCTTGTTTT | 10600 |
rs751982329 | snp | G/T | 8.25934e-05 | 0.00642572 | splice-donor-variant | USP16 | GRCh38.p7 | 21:29042529 | GTTTTAGATGATCAG[G/T]TAAGACTATTGAATT | 10600 |
rs752027576 | snp | A/G | 3.36916e-05 | 0.00410422 | missense, utr-variant-5-prime | USP16 | GRCh38.p7 | 21:29030607 | TAGAACCTGTGTGCA[A/G]ACACATTAGAAAAGG | 10600 |
rs752190889 | snp | C/T | 1.71722e-05 | 0.00293016 | intron-variant | USP16 | GRCh38.p7 | 21:29036401 | TGTTTCTTTAATATA[C/T]ACCAAATGTCGATTT | 10600 |
rs752195964 | snp | A/T | | | upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29022960 | ATAATGTTGTCAGAA[A/T]ACAGAGAAAGATGAA | 10600 |
rs752215347 | in-del | -/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29044666 | GGTCAGGCTGGTCTC[-/T]TAACTCCTGACCTCA | 10600 |
rs752266289 | in-del | -/TAAAGT | 8.86156e-05 | 0.00665582 | cds-indel | USP16 | GRCh38.p7 | 21:29040677 | TGAAGAACTAAAAAA[-/TAAAGT]TAAAGGTAATGTCTG | 10600 |
rs752285296 | snp | A/C | 1.72053e-05 | 0.00293298 | missense | USP16 | GRCh38.p7 | 21:29042101 | GTGTGATCAATGCAG[A/C]ACTGTAAGTAGATGT | 10600 |
rs752406360 | snp | A/C/T | 3.38858e-05 | 0.00411606 | missense | USP16 | GRCh38.p7 | 21:29042030 | TATGAGAAGAAAAAA[A/C/T]CAATGCCAAGTTTTG | 10600 |
rs752454370 | snp | C/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29030172 | CAAAGAAAACAGCTG[C/T]GACTTGGTCAATTTT | 10600 |
rs752514513 | snp | A/C | | | intron-variant | USP16 | GRCh38.p7 | 21:29051021 | TGGGGAGATAGAAGG[A/C]ATATTTCAGGAGGTA | 10600 |
rs752544646 | snp | C/T | 1.64773e-05 | 0.00287026 | synonymous-codon | USP16 | GRCh38.p7 | 21:29054100 | AGGGCAGTGGTTTCA[C/T]ATCAGCGACACACAT | 10600 |
rs752596346 | snp | C/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29044533 | GCACACTGCAACCTC[C/T]GCCTCCCAGGTTCAA | 10600 |
rs752649188 | snp | A/T | 6.60993e-05 | 0.0057485 | missense | USP16 | GRCh38.p7 | 21:29046797 | TAAATATTAAATCCA[A/T]CCATATTTCACAAGA | 10600 |
rs752704721 | snp | C/T | 1.64942e-05 | 0.00287173 | missense, utr-variant-5-prime | USP16 | GRCh38.p7 | 21:29037380 | ATGGCTAAAGAGAAT[C/T]CTCCCATGAATTCTC | 10600 |
rs752706636 | snp | C/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29050446 | GGTGAGCAGATCTAT[C/T]AATGAATAATCTGTT | 10600 |
rs752735443 | snp | C/T | 1.64806e-05 | 0.00287054 | intron-variant | USP16 | GRCh38.p7 | 21:29053995 | AGGCACTCAGCAGAT[C/T]ACGGCAAAACCAAAA | 10600 |
rs752785458 | snp | A/T | 1.65545e-05 | 0.00287697 | missense | USP16 | GRCh38.p7 | 21:29048846 | TCTTCATTTAAAGAG[A/T]TTTCAGCAGGTACTC | 10600 |
rs752911766 | snp | A/C | 1.66985e-05 | 0.00288946 | synonymous-codon, utr-variant-5-prime | USP16 | GRCh38.p7 | 21:29030615 | GTGTGCAGACACATT[A/C]GAAAAGGATTGGAAC | 10600 |
rs752924945 | snp | C/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29049961 | AGTGTTCAGGAAGAA[C/T]TGAGTCTCCAAAGAA | 10600 |
rs752931729 | snp | A/T | 1.69123e-05 | 0.0029079 | intron-variant | USP16 | GRCh38.p7 | 21:29039590 | ATGTTATGACCATTG[A/T]ATTTTATGATCTTAT | 10600 |
rs753043658 | snp | A/G | 6.77576e-05 | 0.00582015 | utr-variant-3-prime | USP16 | GRCh38.p7 | 21:29054237 | ATGGCTTTTATAATG[A/G]CTGAAATAACGATAA | 10600 |
rs753131139 | snp | A/G | 1.65902e-05 | 0.00288008 | intron-variant | USP16 | GRCh38.p7 | 21:29038326 | TTTTTTTTTCACCCT[A/G]CATTCTAGAACTTGT | 10600 |
rs753132155 | snp | C/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29040252 | CCCCCAGAAATAATG[C/G]AGCTGGGCTTTAAGC | 10600 |
rs753146218 | snp | G/T | 1.65425e-05 | 0.00287593 | intron-variant | USP16 | GRCh38.p7 | 21:29038447 | TATGTTCTTTAAACT[G/T]TTCTAGTCTGTAACT | 10600 |
rs753157966 | snp | C/T | 1.79664e-05 | 0.00299714 | synonymous-codon | USP16 | GRCh38.p7 | 21:29043437 | GAGTGGTAAGAAAAG[C/T]GTAAATGATAAAAAT | 10600 |
rs753258791 | snp | A/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29041826 | AATTATGTTATGCTC[A/T]GAGGTGGAATATATA | 10600 |
rs753305068 | in-del | -/C | 0.00103226 | 0.022695 | upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29024586 | GTCAGAGCCGATGGT[-/C]CCGGGAGGTGGGGGT | 10600 |
rs753415484 | snp | G/T | 1.64917e-05 | 0.00287151 | synonymous-codon, utr-variant-5-prime | USP16 | GRCh38.p7 | 21:29037397 | TCCCATGAATTCTCC[G/T]TGCCAAATAACCGTG | 10600 |
rs753514125 | snp | A/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29038897 | TATCTCTTTTGATGT[A/G]CATTTTAAACTTTTA | 10600 |
rs753518659 | snp | C/G | 1.64827e-05 | 0.00287073 | intron-variant | USP16 | GRCh38.p7 | 21:29054006 | AGATTACGGCAAAAC[C/G]AAAAAGTAATCAACT | 10600 |
rs753582894 | in-del | -/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29045939 | GCCTCCCGAGTAGCT[-/G]GGATTACAGGCGCGC | 10600 |
rs753596798 | snp | C/G | | | missense | USP16 | GRCh38.p7 | 21:29043599 | CAAAAAGCAAGCCAA[C/G]GTGGGTAATTAGGAG | 10600 |
rs753620226 | snp | A/G | 3.42648e-05 | 0.00413899 | synonymous-codon | USP16 | GRCh38.p7 | 21:29040653 | TGGTAATTCTACTGA[A/G]AAGTTGGATGAAGAA | 10600 |
rs753677979 | snp | A/G | 1.6489e-05 | 0.00287128 | stop-gained, utr-variant-5-prime | USP16 | GRCh38.p7 | 21:29030667 | TAGTGAATGTGGAAT[A/G]GAATATCTGCCAAGA | 10600 |
rs753708938 | snp | A/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29033755 | TAACGTTAGTACAAG[A/G]TAAAAAATAAGGAAT | 10600 |
rs753711150 | snp | A/G | 1.6552e-05 | 0.00287676 | missense | USP16 | GRCh38.p7 | 21:29046986 | CTAGGAATTTAAATG[A/G]TGCCTACCTAACGGA | 10600 |
rs753745265 | in-del | -/TTA | | | intron-variant | USP16 | GRCh38.p7 | 21:29051944 | AAGGTACATGATCAT[-/TTA]TTATACTTTTGTTTC | 10600 |
rs753757001 | in-del | -/T | 1.87068e-05 | 0.00305828 | intron-variant | USP16 | GRCh38.p7 | 21:29037501 | TTAAAAAAGCTGTCC[-/T]TTTCCTCATAGAATC | 10600 |
rs753825587 | snp | A/G | 4.96003e-05 | 0.00497973 | missense | USP16 | GRCh38.p7 | 21:29046916 | TCCACAGAGGAAGTA[A/G]ATATGAAAAATATCA | 10600 |
rs753829416 | snp | A/C | | | intron-variant | USP16 | GRCh38.p7 | 21:29035078 | CACTTTCACAAAGCT[A/C]AAGAATGCAGTATTA | 10600 |
rs753916870 | snp | A/G | 1.70438e-05 | 0.00291918 | missense | USP16 | GRCh38.p7 | 21:29043589 | AGAAACAAGCCAAAA[A/G]GCAAGCCAAGGTGGG | 10600 |
rs753930199 | snp | A/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29039751 | GAATCCAGAGAATTA[A/G]CAGTAATTCTCTTTC | 10600 |
rs753965965 | snp | G/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29041634 | TTGAATGTTAGAATG[G/T]TAGAGCTAGAACTAA | 10600 |
rs754049557 | snp | C/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29025181 | CACTTATCCAATTGA[C/T]TATATCTAGGAGGGG | 10600 |
rs754055833 | snp | C/T | 6.61529e-05 | 0.00575083 | missense | USP16 | GRCh38.p7 | 21:29050135 | AACACATAAAGTTTC[C/T]GGAAATCTTAGATTT | 10600 |
rs754066176 | snp | A/C | 1.67649e-05 | 0.0028952 | intron-variant | USP16 | GRCh38.p7 | 21:29048870 | GGTACTCCTTGTTAC[A/C]CAAAATTTGTTTTAA | 10600 |
rs754084000 | snp | C/G | 1.65723e-05 | 0.00287852 | intron-variant | USP16 | GRCh38.p7 | 21:29034793 | CATTCTCCCCTCTTG[C/G]TGAGTTTTTATGGCT | 10600 |
rs754094854 | in-del | -/A | | | intron-variant | USP16 | GRCh38.p7 | 21:29025202 | TAGGAGGGGATTGAT[-/A]ATACGCAAAACTTGA | 10600 |
rs754159477 | snp | A/G | 1.64882e-05 | 0.00287121 | missense | USP16 | GRCh38.p7 | 21:29047123 | ACTCCTGGAACAAAG[A/G]TGTATGAGGTTGTAA | 10600 |
rs754280653 | snp | A/G | 6.63489e-05 | 0.00575935 | intron-variant, upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29027830 | AGAGAAATATAAGAC[A/G]TACTTTTTTTTTTGG | 10600 |
rs754282555 | in-del | -/GT | | | intron-variant | USP16 | GRCh38.p7 | 21:29048051 | TCAGAGACGATACGT[-/GT]GTGTGTGTGTGTGTG | 10600 |
rs754298425 | in-del | -/GTAA | 1.83303e-05 | 0.00302734 | intron-variant | USP16 | GRCh38.p7 | 21:29047341 | TTTAATGCTCTCACT[-/GTAA]GTAAAATTAATATTC | 10600 |
rs754398166 | snp | A/T | 1.99281e-05 | 0.00315652 | intron-variant | USP16 | GRCh38.p7 | 21:29046628 | TTCTCCCGCTCTTTC[A/T]TTTTCTTTATTTTTT | 10600 |
rs754406539 | in-del | -/TATTTTA | 1.65293e-05 | 0.00287479 | frameshift-variant | USP16 | GRCh38.p7 | 21:29054165 | CACAAGCGTACCTCC[-/TATTTTA]TGAGAGAATACTGTA | 10600 |
rs754412387 | snp | C/G/T | 3.41298e-05 | 0.00413086 | intron-variant | USP16 | GRCh38.p7 | 21:29038984 | TAAAGTCAGTGATTC[C/G/T]AGAATTTGACTGAAG | 10600 |
rs754457824 | snp | C/G | 1.74671e-05 | 0.00295521 | intron-variant | USP16 | GRCh38.p7 | 21:29050210 | TTTTTCAGGAAAGTC[C/G]TTTAAAGTCAAATTG | 10600 |
rs754469807 | snp | A/C | 1.67728e-05 | 0.00289588 | intron-variant | USP16 | GRCh38.p7 | 21:29036234 | CCCTTTTTAGTTGTC[A/C]TTTTGTCATTTTTCA | 10600 |
rs754530345 | snp | A/C | | | intron-variant, upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29026437 | CTCCGGCCTGGGCGA[A/C]AGAGCAAGACTCCGT | 10600 |
rs754543674 | in-del | -/AC | | | intron-variant | USP16 | GRCh38.p7 | 21:29034708 | TGATTCTAGAGTCTA[-/AC]ATTTTCTTTTCAAGA | 10600 |
rs754594288 | snp | A/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29042671 | GTAGAATGCATTTTA[A/G]GATTTGAATAAAGAA | 10600 |
rs754636715 | snp | A/G | 3.78351e-05 | 0.00434927 | intron-variant | USP16 | GRCh38.p7 | 21:29040710 | CTGACTTTTTGAACT[A/G]AAACACTATAGTTGA | 10600 |
rs754649290 | snp | A/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29043704 | TGTTATTTTAGATAC[A/G]GCACTTTCATTTGAC | 10600 |
rs754750995 | snp | A/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29041307 | GCCAGTAATGGAGAG[A/G]ATTACCCCTGCTGGC | 10600 |
rs754754780 | snp | A/G | 1.6528e-05 | 0.00287467 | synonymous-codon | USP16 | GRCh38.p7 | 21:29046792 | AGAAGTAAATATTAA[A/G]TCCAACCATATTTCA | 10600 |
rs754760254 | snp | C/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29048175 | GCAATCTCCACCTCC[C/T]GGGTTCAAGAGATTC | 10600 |
rs754774959 | snp | C/T | 9.25095e-05 | 0.00680046 | intron-variant | USP16 | GRCh38.p7 | 21:29046657 | TTGATGCCGTATACT[C/T]TTTACCCAGAACCAA | 10600 |
rs754779369 | snp | G/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29033848 | CATCTGGGAGATAAG[G/T]ATAGGCTTCTGGGAG | 10600 |
rs754822777 | snp | C/G | 1.64874e-05 | 0.00287113 | missense | USP16 | GRCh38.p7 | 21:29053836 | CAAGGGTACTCTATT[C/G]CTTATATGGAGTTGT | 10600 |
rs754903851 | snp | A/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29035083 | TCACAAAGCTAAAGA[A/G]TGCAGTATTATGAGA | 10600 |
rs755015912 | snp | C/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29025224 | AAAACTTGAAAGCCA[C/T]GTTAACACCTGCTGA | 10600 |
rs755024403 | snp | A/G | 1.70368e-05 | 0.00291858 | intron-variant | USP16 | GRCh38.p7 | 21:29036395 | ATAATTTGTTTCTTT[A/G]ATATACACCAAATGT | 10600 |
rs755030216 | snp | A/G | 1.65438e-05 | 0.00287605 | synonymous-codon | USP16 | GRCh38.p7 | 21:29047257 | GAAACTTCGAGATGC[A/G]AATAAACTGCTTTGT | 10600 |
rs755042356 | snp | A/C | 1.81069e-05 | 0.00300884 | intron-variant | USP16 | GRCh38.p7 | 21:29027999 | ATTGATTGAATCTTT[A/C]ATGTTTATATCTCTA | 10600 |
rs755084466 | snp | C/T | 3.36672e-05 | 0.00410274 | intron-variant | USP16 | GRCh38.p7 | 21:29048746 | TCCCTGTTAAAAATT[C/T]CTTCTTTTCTTTAGG | 10600 |
rs755330725 | snp | A/G | 1.88163e-05 | 0.00306721 | missense | USP16 | GRCh38.p7 | 21:29043427 | TATATTTTAAGAGTG[A/G]TAAGAAAAGTGTAAA | 10600 |
rs755356644 | snp | C/G | 1.65083e-05 | 0.00287296 | missense, utr-variant-5-prime | USP16 | GRCh38.p7 | 21:29037419 | ATAACCGTGAAAGGA[C/G]TCAGTAATTTGGGAA | 10600 |
rs755384261 | snp | A/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29036039 | CCAGTAAAGTAAAAC[A/G]TTTGGAGTATTTCAT | 10600 |
rs755391422 | snp | A/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29052993 | CCTGTCTCAAAAAAA[A/T]TTTTATGAAGTTGAA | 10600 |
rs755442642 | snp | C/T | | | missense | USP16 | GRCh38.p7 | 21:29053950 | TTCTTCACGGTGATA[C/T]TCCACAAGGTAAGAT | 10600 |
rs755461054 | in-del | -/TAA | 1.65938e-05 | 0.00288039 | cds-indel | USP16 | GRCh38.p7 | 21:29054185 | TATGAGAGAATACTG[-/TAA]TAATATCAAAAGCAC | 10600 |
rs755478706 | snp | A/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29038159 | AAGCTCAGAACTGAA[A/G]TAGTTATGACCCAAA | 10600 |
rs755559590 | snp | C/T | 1.65362e-05 | 0.00287538 | intron-variant | USP16 | GRCh38.p7 | 21:29042535 | GATGATCAGGTAAGA[C/T]TATTGAATTTATTTT | 10600 |
rs755574170 | snp | C/T | 3.29647e-05 | 0.00405971 | intron-variant | USP16 | GRCh38.p7 | 21:29053997 | GCACTCAGCAGATTA[C/T]GGCAAAACCAAAAAG | 10600 |
rs755644897 | snp | A/G | 5.3126e-05 | 0.00515366 | missense | USP16 | GRCh38.p7 | 21:29046674 | TTACCCAGAACCAAC[A/G]AAGACAACAAAAAAT | 10600 |
rs755665311 | snp | A/G | 1.64743e-05 | 0.00287 | missense | USP16 | GRCh38.p7 | 21:29053868 | GAACACAGTGGTACT[A/G]TGAGGTCGGGGCATT | 10600 |
rs755718380 | snp | C/T | | | downstream-variant-500B | USP16 | GRCh38.p7 | 21:29054703 | CTGCAAGCTCTGCCT[C/T]CTAGGTTCACGCCAT | 10600 |
rs755772278 | snp | C/T | 0.000296922 | 0.0121808 | synonymous-codon, utr-variant-5-prime | USP16 | GRCh38.p7 | 21:29036277 | GGGTCACAGGTGTTA[C/T]GTATGTGATAATGAG | 10600 |
rs755828805 | snp | A/T | 1.72083e-05 | 0.00293323 | missense | USP16 | GRCh38.p7 | 21:29042102 | TGTGATCAATGCAGA[A/T]CTGTAAGTAGATGTC | 10600 |
rs755841884 | snp | G/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29039598 | ACCATTGTATTTTAT[G/T]ATCTTATCTTCATAA | 10600 |
rs755926892 | snp | A/C/T | 6.60397e-05 | 0.00574596 | missense, utr-variant-5-prime | USP16 | GRCh38.p7 | 21:29039530 | AGCCAGGAGCTGCTT[A/C/T]GCTACTTATTGGATG | 10600 |
rs755966427 | snp | A/C | 3.30513e-05 | 0.00406504 | missense | USP16 | GRCh38.p7 | 21:29046900 | AACTGACAATCAAAA[A/C]TCCACAGAGGAAGTA | 10600 |
rs756018676 | snp | C/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29047770 | TTTCCCTTATCTCCC[C/G]ATTGCTTTTTTTTTT | 10600 |
rs756054777 | snp | A/G | 0.000165207 | 0.00908715 | missense | USP16 | GRCh38.p7 | 21:29046800 | ATATTAAATCCAACC[A/G]TATTTCACAAGAGGG | 10600 |
rs756108738 | snp | G/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29036940 | CATGTCCATGTTCTT[G/T]ATTGTTTTATATTCT | 10600 |
rs756163469 | snp | C/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29038038 | ATATAGAAGCAAATA[C/T]GTACCTACAGGTAGT | 10600 |
rs756227936 | in-del | -/A | | | intron-variant | USP16 | GRCh38.p7 | 21:29053477 | GTATTCAGAGTTGTT[-/A]ATAGCTAGGGTTGTT | 10600 |
rs756266530 | snp | C/G | 8.33396e-05 | 0.00645468 | intron-variant | USP16 | GRCh38.p7 | 21:29048862 | TTTCAGCAGGTACTC[C/G]TTGTTACCCAAAATT | 10600 |
rs756266930 | snp | A/C | 1.65537e-05 | 0.0028769 | intron-variant | USP16 | GRCh38.p7 | 21:29042541 | CAGGTAAGACTATTG[A/C]ATTTATTTTATTCAA | 10600 |
rs756288725 | snp | C/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29027978 | CTGAAACTTTAGGTA[C/T]ATTTCATTGATTGAA | 10600 |
rs756358518 | snp | A/G | 6.62592e-05 | 0.00575545 | missense | USP16 | GRCh38.p7 | 21:29048766 | TTTTCTTTAGGTGAA[A/G]GGAAGCATGTTTACA | 10600 |
rs756386366 | snp | A/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29028725 | CAGGCGTGAGCCACC[A/G]CGCCCGACCTTCAAC | 10600 |
rs756386941 | snp | C/T | 1.66018e-05 | 0.00288108 | synonymous-codon, utr-variant-5-prime | USP16 | GRCh38.p7 | 21:29030624 | CACATTAGAAAAGGA[C/T]TGGAACAAGGTAATT | 10600 |
rs756407259 | in-del | -/GTT | 1.65359e-05 | 0.00287536 | cds-indel | USP16 | GRCh38.p7 | 21:29047034 | TGGACATTTCCAATG[-/GTT]TCAAAAACCTAAATT | 10600 |
rs756433198 | snp | A/G | 1.65509e-05 | 0.00287666 | missense | USP16 | GRCh38.p7 | 21:29047004 | CCTACCTAACGGAAG[A/G]GAGCAATGGAGAAGT | 10600 |
rs756454760 | snp | A/T | | | intron-variant, utr-variant-5-prime | USP16 | GRCh38.p7 | 21:29025018 | CCAGAGGTTCCCCCG[A/T]GGGATCGGAGCAGTT | 10600 |
rs756477676 | snp | C/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29030018 | TACTATTATTATCTT[C/T]TAGGATTGCACAGAT | 10600 |
rs756495585 | snp | A/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29045053 | TAGATGGAAAATATT[A/G]TCTCAGTGCAGTTTT | 10600 |
rs756504347 | snp | A/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29030001 | ATATCAGCAATTTTT[A/G]TTACTATTATTATCT | 10600 |
rs756573083 | snp | A/T | 1.64857e-05 | 0.00287099 | missense | USP16 | GRCh38.p7 | 21:29054138 | CTGTGCCTACAACTA[A/T]AGTACTAAACTCACA | 10600 |
rs756603313 | in-del | -/T | 3.34345e-05 | 0.00408853 | intron-variant | USP16 | GRCh38.p7 | 21:29042562 | TTTTATTCAAGTAGA[-/T]TTTTTTTCCTGTAAG | 10600 |
rs756625131 | snp | A/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29051688 | ATACAAAAATTAGCC[A/T]GGCATGGTGGTGTGC | 10600 |
rs756669952 | snp | C/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29030818 | ATTTTAGAAAACTCT[C/T]TGAACTTACTTTAGA | 10600 |
rs756694855 | snp | G/T | 1.65348e-05 | 0.00287526 | missense, utr-variant-5-prime | USP16 | GRCh38.p7 | 21:29038341 | ACATTCTAGAACTTG[G/T]CACAAACACCAGTGC | 10600 |
rs756793425 | snp | A/G | 1.65179e-05 | 0.00287379 | missense | USP16 | GRCh38.p7 | 21:29046811 | AACCATATTTCACAA[A/G]AGGGTGTTATGCATA | 10600 |
rs756810460 | snp | A/G | 1.65353e-05 | 0.00287531 | missense | USP16 | GRCh38.p7 | 21:29046917 | CCACAGAGGAAGTAG[A/G]TATGAAAAATATCAA | 10600 |
rs756930263 | in-del | -/CG | | | intron-variant | USP16 | GRCh38.p7 | 21:29048048 | AGCTCAGAGACGATA[-/CG]TGTGTGTGTGTGTGT | 10600 |
rs756948382 | snp | A/G | 1.64936e-05 | 0.00287168 | missense, utr-variant-5-prime | USP16 | GRCh38.p7 | 21:29037404 | AATTCTCCTTGCCAA[A/G]TAACCGTGAAAGGAC | 10600 |
rs757011109 | snp | C/G/T | | | upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29023136 | TGTGGTGGGGTGGCA[C/G/T]GTGCCTATAATCCCA | 10600 |
rs757035957 | snp | A/G | 3.29728e-05 | 0.00406021 | missense, utr-variant-5-prime | USP16 | GRCh38.p7 | 21:29030670 | TGAATGTGGAATGGA[A/G]TATCTGCCAAGACTG | 10600 |
rs757069997 | snp | A/T | 1.69786e-05 | 0.0029136 | intron-variant | USP16 | GRCh38.p7 | 21:29048888 | AAATTTGTTTTAAAT[A/T]TGTAACACCTACTTT | 10600 |
rs757092738 | snp | A/G | 1.72716e-05 | 0.00293862 | missense | USP16 | GRCh38.p7 | 21:29040661 | CTACTGAAAAGTTGG[A/G]TGAAGAACTAAAAAA | 10600 |
rs757093886 | snp | A/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29050747 | GAGTTGAGAAATGAA[A/G]CCAGAGAAGTGAGAT | 10600 |
rs757109506 | snp | A/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29045849 | GTCACTTTGTTGCCC[A/G]GGCTGGAGTGCAGTG | 10600 |
rs757195021 | snp | C/G | 5.22071e-05 | 0.00510889 | intron-variant | USP16 | GRCh38.p7 | 21:29039615 | TCTTATCTTCATAAG[C/G]TTTCTGTCTCATTTG | 10600 |
rs757238689 | in-del | -/GTAA | | | intron-variant | USP16 | GRCh38.p7 | 21:29052058 | TGGAGGAGATTATTT[-/GTAA]GTGATACATGTGATT | 10600 |
rs757356817 | in-del | -/CTT | | | intron-variant | USP16 | GRCh38.p7 | 21:29044437 | TTTTAGTATATAAAA[-/CTT]CTTCATTCTTTTTTT | 10600 |
rs757441209 | snp | C/G | 1.71717e-05 | 0.00293011 | missense | USP16 | GRCh38.p7 | 21:29043595 | AAGCCAAAAAGCAAG[C/G]CAAGGTGGGTAATTA | 10600 |
rs757466172 | snp | A/G | 3.30797e-05 | 0.00406679 | synonymous-codon | USP16 | GRCh38.p7 | 21:29050136 | ACACATAAAGTTTCC[A/G]GAAATCTTAGATTTG | 10600 |
rs757525231 | snp | A/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29036610 | ATTAATGCTAAGACT[A/G]AGGTAATTCCCATAA | 10600 |
rs757600892 | snp | A/T | 1.72457e-05 | 0.00293642 | missense | USP16 | GRCh38.p7 | 21:29043452 | TGTAAATGATAAAAA[A/T]CTGAAAAAGACAGTG | 10600 |
rs757601980 | in-del | -/AATTGTAAAAATTG | 1.6492e-05 | 0.00287154 | frameshift-variant, utr-variant-5-prime | USP16 | GRCh38.p7 | 21:29038394 | GAAAATGTCTGGAAC[-/AATTGTAAAAATTG]AACCACCTGATTTGG | 10600 |
rs757611880 | in-del | -/T | 0.000137071 | 0.00827748 | intron-variant | USP16 | GRCh38.p7 | 21:29041997 | TGGTAATTGATAGAC[-/T]TTTTTTTCTCCATAG | 10600 |
rs757622839 | snp | C/T | 1.64879e-05 | 0.00287118 | missense | USP16 | GRCh38.p7 | 21:29047124 | CTCCTGGAACAAAGG[C/T]GTATGAGGTTGTAAA | 10600 |
rs757634317 | snp | C/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29029404 | GGCAACAGAGCAAGA[C/T]TCCGTCTCAAAAAGA | 10600 |
rs757635138 | snp | A/T | | | intron-variant, upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29026927 | GAATTTATAAAGGCC[A/T]ATGAGTGCAAAGTTT | 10600 |
rs757659058 | snp | C/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29043250 | CTCATTATGTGAAGA[C/T]TGCTTTCTAGTGTAT | 10600 |
rs757757994 | snp | A/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29028651 | ATGTTGACCAGGCTG[A/G]TCTTGAACTCCTGAC | 10600 |
rs757811437 | snp | G/T | 2.01193e-05 | 0.00317163 | intron-variant, upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29027838 | ATAAGACATACTTTT[G/T]TTTTTGGTCAAGCTA | 10600 |
rs757931604 | snp | C/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29029240 | AACACGGTGAAACCC[C/T]GTCTCTACTAAACAT | 10600 |
rs757974994 | snp | A/G | 5.25758e-05 | 0.0051269 | synonymous-codon | USP16 | GRCh38.p7 | 21:29040671 | GTTGGATGAAGAACT[A/G]AAAAATAAAGTTAAA | 10600 |
rs757991415 | snp | A/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29045387 | TTTCCTCTATTTGGA[A/G]GTAGGTTGCAAGTGG | 10600 |
rs758108095 | in-del | -/TTTTTTTTC | 1.95211e-05 | 0.00312413 | intron-variant | USP16 | GRCh38.p7 | 21:29038312 | AAATAATTTTTCTCT[-/TTTTTTTTC]ACCCTACATTCTAGA | 10600 |
rs758116008 | snp | A/C | | | intron-variant | USP16 | GRCh38.p7 | 21:29030396 | AAGAAAGCGAAACTT[A/C]ACAAATTTGTGTCAA | 10600 |
rs758129005 | snp | A/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29036387 | CAGGTAAAATAATTT[A/G]TTTCTTTAATATACA | 10600 |
rs758169185 | snp | A/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29031965 | CTTCTTTTTTTGTGC[A/G]TGTGTGTATGTGTAC | 10600 |
rs758212919 | snp | A/C | 1.74321e-05 | 0.00295224 | intron-variant | USP16 | GRCh38.p7 | 21:29043606 | CAAGCCAAGGTGGGT[A/C]ATTAGGAGGAAAATC | 10600 |
rs758242028 | snp | A/G | 1.65433e-05 | 0.002876 | intron-variant | USP16 | GRCh38.p7 | 21:29034974 | GCCTCTTGGGTGGAA[A/G]TTATTTGAAATATTA | 10600 |
rs758279144 | snp | A/G | | | missense | USP16 | GRCh38.p7 | 21:29042048 | ATGCCAAGTTTTGTT[A/G]ACCGCATCTTTGGTG | 10600 |
rs758312813 | snp | A/G | 1.64974e-05 | 0.00287201 | intron-variant | USP16 | GRCh38.p7 | 21:29034818 | ATGGCTTTGAGGTTT[A/G]TGATTATGATTTTTT | 10600 |
rs758379169 | in-del | -/CAC | | | intron-variant | USP16 | GRCh38.p7 | 21:29051506 | GGTAGAAAGTGAGGA[-/CAC]CACAAAGGATCTCAA | 10600 |
rs758427590 | snp | G/T | 3.31384e-05 | 0.00407039 | intron-variant | USP16 | GRCh38.p7 | 21:29039161 | GTCTGTAAAAAGTGA[G/T]TATCCACTTCGATTG | 10600 |
rs758460738 | snp | A/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29048299 | CGTTGGCCAGGGTGG[A/T]CTCAAACTCCTAACC | 10600 |
rs758482271 | snp | C/T | 0.000127144 | 0.00797221 | intron-variant, upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29027868 | AACTTTATCTTGTTT[C/T]CTAGATTGTTATTTT | 10600 |
rs758614983 | snp | C/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29050016 | TATTCTTTTGGACGT[C/T]GGAGGGGACTTCGGT | 10600 |
rs758650074 | snp | A/T | | | missense | USP16 | GRCh38.p7 | 21:29054126 | CACATGTGCAAGCTG[A/T]GCCTACAACTAAAGT | 10600 |
rs758657793 | in-del | -/G | 1.68618e-05 | 0.00290356 | intron-variant | USP16 | GRCh38.p7 | 21:29048879 | TGTTACCCAAAATTT[-/G]TTTTAAATATGTAAC | 10600 |
rs758682462 | snp | A/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29039018 | GTAATTTCTTTTCCC[A/T]TATTCAGGAACCATT | 10600 |
rs758699448 | snp | A/G | 2.41876e-05 | 0.00347753 | intron-variant | USP16 | GRCh38.p7 | 21:29037229 | TATACTTCTGCATTC[A/G]ATATGACTGTATTAC | 10600 |
rs758752875 | snp | A/G | 1.65127e-05 | 0.00287334 | missense | USP16 | GRCh38.p7 | 21:29042524 | TCCCAGTTTTAGATG[A/G]TCAGGTAAGACTATT | 10600 |
rs758772972 | snp | A/C | | | intron-variant | USP16 | GRCh38.p7 | 21:29040297 | CTGTGGCTGTCATGT[A/C]ATCATTGTGCTTGTA | 10600 |
rs758789634 | snp | A/T | 5.27477e-05 | 0.00513528 | intron-variant | USP16 | GRCh38.p7 | 21:29042113 | CAGAACTGTAAGTAG[A/T]TGTCATGTATACTGG | 10600 |
rs758871608 | in-del | -/T/TT | 0.243001 | 0.249936 | intron-variant, upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29027833 | AAATATAAGACATAC[-/T/TT]TTTTTTTTTTGGTCA | 10600 |
rs758897921 | snp | A/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29025476 | GATGGAAGTCACAAT[A/G]TGCTCTCCTCATGAC | 10600 |
rs758899913 | snp | C/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29041940 | AGTTAGATAGGTAAG[C/T]AGTTTTAGCTTTTCT | 10600 |
rs758912563 | snp | C/T | 1.71141e-05 | 0.00292519 | synonymous-codon | USP16 | GRCh38.p7 | 21:29042098 | CATGTGTGATCAATG[C/T]AGAACTGTAAGTAGA | 10600 |
rs758919423 | in-del | -/TTTTTTT | | | downstream-variant-500B | USP16 | GRCh38.p7 | 21:29054603 | ACAAGTGTGTTAATT[-/TTTTTTT]TTTTTTTTTTTTTTT | 10600 |
rs758949140 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29026788 | GTTGTTATGAAAATC[C/T]GATGTGATAATGTTT | 10600 |
rs758990355 | snp | A/G | 3.30409e-05 | 0.0040644 | missense | USP16 | GRCh38.p7 | 21:29047243 | TTCACCCGTAATGAG[A/G]AACTTCGAGATGCGA | 10600 |
rs759013552 | in-del | -/AT | | | intron-variant | USP16 | GRCh38.p7 | 21:29037509 | GCTGTCCTTTTCCTC[-/AT]AGAATCTGCTACTTA | 10600 |
rs759073692 | snp | A/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29037517 | TTTCCTCATAGAATC[A/T]GCTACTTACATTATT | 10600 |
rs759128878 | snp | A/G | | | upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29022651 | TGGTACAATGACCCT[A/G]AGGCTCTGTTTTAAA | 10600 |
rs759181086 | snp | A/T | 1.67944e-05 | 0.00289775 | intron-variant | USP16 | GRCh38.p7 | 21:29039472 | TTCTGTCTTTTTGTT[A/T]TTCTCTAGAGCAGTG | 10600 |
rs759240751 | snp | A/T | 3.29538e-05 | 0.00405904 | missense | USP16 | GRCh38.p7 | 21:29054075 | TGACAGATTTTGAAA[A/T]GGAATCAAAAGGGCA | 10600 |
rs759303643 | snp | G/T | 0.000245972 | 0.0110872 | intron-variant, upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29024814 | TGGCAGTCGTCGCTC[G/T]CCTGGCTTTCTGCGC | 10600 |
rs759360107 | snp | C/T | 1.91565e-05 | 0.00309482 | intron-variant | USP16 | GRCh38.p7 | 21:29037506 | AAAGCTGTCCTTTTC[C/T]TCATAGAATCTGCTA | 10600 |
rs759375147 | snp | C/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29028726 | AGGCGTGAGCCACCG[C/T]GCCCGACCTTCAACA | 10600 |
rs759381216 | snp | A/G | 1.64789e-05 | 0.0028704 | intron-variant | USP16 | GRCh38.p7 | 21:29053975 | TAAGATGTCTTGGAA[A/G]ATTCAGGCACTCAGC | 10600 |
rs759439271 | snp | A/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29052194 | TCAGGTGATGCTGAT[A/G]CTGGCTGTTCATGGA | 10600 |
rs759509975 | snp | A/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29050919 | GCTGAATTTTAGGAC[A/G]GAAAGACTAGAGGTG | 10600 |
rs759510075 | in-del | -/TA | 0.000789993 | 0.0198588 | intron-variant | USP16 | GRCh38.p7 | 21:29040579 | TTTAAAATTTAATAG[-/TA]TATATATATATCCAT | 10600 |
rs759519134 | snp | A/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29036170 | GGTTTCTTTAATAGA[A/G]TAAGTTGGCAGTTAC | 10600 |
rs759604143 | snp | A/G | 3.36479e-05 | 0.00410157 | synonymous-codon, utr-variant-5-prime | USP16 | GRCh38.p7 | 21:29030608 | AGAACCTGTGTGCAG[A/G]CACATTAGAAAAGGA | 10600 |
rs759633972 | snp | C/T | 1.65474e-05 | 0.00287636 | missense | USP16 | GRCh38.p7 | 21:29046961 | CTGGAGGTTTTAACA[C/T]CTTCTCCCACTAGGA | 10600 |
rs759671004 | snp | C/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29053318 | AGCAGCGTGCACTCT[C/G]TCGTGGGGAAAGTGA | 10600 |
rs759713041 | snp | A/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29028222 | CGCCTCCCAGGTTCA[A/G]ACGGTTCTCTCGTGC | 10600 |
rs759787682 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29026621 | TTCTGGCCTCAAGCC[A/G]TCCTCCCACCTCGAT | 10600 |
rs759793209 | snp | A/G | 1.65173e-05 | 0.00287374 | missense | USP16 | GRCh38.p7 | 21:29046877 | CAAGCAAAAATGATC[A/G]AAAGTGTAACTGACA | 10600 |
rs759887857 | snp | C/G | 1.66045e-05 | 0.00288132 | missense | USP16 | GRCh38.p7 | 21:29043522 | GACAGTTACATAAAA[C/G]AGAGAAGTGATATTC | 10600 |
rs759976028 | in-del | -/AG | | | splice-acceptor-variant, upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29027871 | TTTATCTTGTTTTCT[-/AG]ATTGTTATTTTGTGT | 10600 |
rs760006932 | snp | A/C | | | intron-variant | USP16 | GRCh38.p7 | 21:29033413 | AGAAATTACCAATGT[A/C]TATTTCTTCTCCAAA | 10600 |
rs760011190 | snp | A/G | 1.6522e-05 | 0.00287414 | missense | USP16 | GRCh38.p7 | 21:29048823 | TCTCTTGCTCCTCCT[A/G]TTCTTACTCTTCATT | 10600 |
rs760050207 | snp | A/G | 8.24613e-05 | 0.00642058 | missense, utr-variant-5-prime | USP16 | GRCh38.p7 | 21:29037386 | AAAGAGAATCCTCCC[A/G]TGAATTCTCCTTGCC | 10600 |
rs760107759 | snp | C/T | 1.64868e-05 | 0.00287109 | intron-variant | USP16 | GRCh38.p7 | 21:29043398 | GTAAAATTTTGTTTT[C/T]GACCTATGTTATCTA | 10600 |
rs760110829 | snp | A/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29034547 | CGAACTCCTGACCTC[A/G]GGTGATCCCACCCCT | 10600 |
rs760127633 | in-del | -/TTC | | | intron-variant | USP16 | GRCh38.p7 | 21:29049569 | CGAGAAAAGTTGTTT[-/TTC]TTCTTTTTGAAACAG | 10600 |
rs760132502 | snp | C/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29049587 | TTCTTTTTGAAACAG[C/T]CTTGTTCTGTCACCC | 10600 |
rs760195246 | snp | C/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29047759 | CATACTGACAATTTC[C/G]CTTATCTCCCCATTG | 10600 |
rs760258427 | snp | A/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29038039 | TATAGAAGCAAATAC[A/G]TACCTACAGGTAGTG | 10600 |
rs760326248 | snp | A/T | 1.65526e-05 | 0.00287681 | missense | USP16 | GRCh38.p7 | 21:29046976 | TCTTCTCCCACTAGG[A/T]ATTTAAATGGTGCCT | 10600 |
rs760357127 | snp | G/T | 3.86264e-05 | 0.00439451 | intron-variant | USP16 | GRCh38.p7 | 21:29047363 | AAATTAATATTCAGG[G/T]GCACATTTTGCACTG | 10600 |
rs760414102 | snp | A/G | 1.65433e-05 | 0.002876 | missense | USP16 | GRCh38.p7 | 21:29054171 | CGTACCTCCTATTTT[A/G]TGAGAGAATACTGTA | 10600 |
rs760422324 | in-del | -/C | 1.74239e-05 | 0.00295155 | intron-variant | USP16 | GRCh38.p7 | 21:29039454 | GTAGACTGAAGATTG[-/C]TTTTCTGTCTTTTTG | 10600 |
rs760464211 | in-del | -/T | 0.00012227 | 0.00781792 | intron-variant | USP16 | GRCh38.p7 | 21:29037474 | GCAGGTACATTGTCA[-/T]TTTTTTTCCCTTTAA | 10600 |
rs760466677 | snp | C/T | 1.94297e-05 | 0.00311681 | intron-variant | USP16 | GRCh38.p7 | 21:29030559 | GAAAGTCATTTTTGA[C/T]CTTATATATTCCTTG | 10600 |
rs760577254 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29026312 | AATACAAAAATTAGC[C/T]GGGTGTGGTGGTGGG | 10600 |
rs760630243 | snp | A/G | | | utr-variant-5-prime, upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29027903 | CAGTAAGTAATCCAT[A/G]AAGTGCCAACATGGG | 10600 |
rs760659507 | snp | C/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29047643 | CCTTTGCACCCAGGA[C/T]GCCACACTTGAATTT | 10600 |
rs760736832 | snp | A/G | 1.82493e-05 | 0.00302065 | intron-variant | USP16 | GRCh38.p7 | 21:29038286 | AGAAGTGTCAGAGTT[A/G]ATTTGCCTTTAAATA | 10600 |
rs760824206 | snp | A/G | 3.31334e-05 | 0.00407009 | missense | USP16 | GRCh38.p7 | 21:29050111 | GTTTTAACCTACGCA[A/G]AGTTAACAAACACAT | 10600 |
rs760859986 | snp | C/G | 1.66065e-05 | 0.00288149 | intron-variant | USP16 | GRCh38.p7 | 21:29034786 | GATTATGCATTCTCC[C/G]CTCTTGCTGAGTTTT | 10600 |
rs760860379 | snp | A/C | 2.23202e-05 | 0.0033406 | intron-variant | USP16 | GRCh38.p7 | 21:29041973 | TTTAATTAATTATAT[A/C]ACGGTAATTGGTAAT | 10600 |
rs760949508 | snp | C/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29039680 | TTAAGGCCATCATAC[C/T]TTAAAATTTTTTCTT | 10600 |
rs760992544 | in-del | -/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29044449 | AAACTTCTTCATTCT[-/T]TTTTTTTTTTTTTTT | 10600 |
rs761022126 | snp | A/G | 1.65304e-05 | 0.00287488 | missense | USP16 | GRCh38.p7 | 21:29047039 | ATTTCCAATGGTTTC[A/G]AAAACCTAAATTTGA | 10600 |
rs761054310 | in-del | -/TT | 1.64864e-05 | 0.00287105 | frameshift-variant | USP16 | GRCh38.p7 | 21:29054137 | CTGTGCCTACAACTA[-/TT]AAGTACTAAACTCAC | 10600 |
rs761121516 | snp | A/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29046547 | TATTTTTGATTGACA[A/G]GCAGCAAAACTGGAT | 10600 |
rs761168663 | in-del | -/A | | | upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29023050 | GGATCACTTGAGGCC[-/A]AGGAGTTCAAGACCA | 10600 |
rs761172015 | in-del | -/AC | 4.94332e-05 | 0.00497133 | frameshift-variant | USP16 | GRCh38.p7 | 21:29054108 | GGTTTCACATCAGCG[-/AC]ACACATGTGCAAGCT | 10600 |
rs761243442 | snp | C/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29047696 | CCCAGTGCAAAGCAC[C/T]GGGAAGACAGTGCTT | 10600 |
rs761246119 | snp | C/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29047428 | GGATGGCATGAATAA[C/G]TGTCCTTTTCTGTGT | 10600 |
rs761254448 | snp | A/G | 1.64933e-05 | 0.00287165 | missense, utr-variant-5-prime | USP16 | GRCh38.p7 | 21:29038398 | ATGTCTGGAACAATT[A/G]TAAAAATTGAACCAC | 10600 |
rs761303051 | snp | C/T | 1.66846e-05 | 0.00288826 | missense | USP16 | GRCh38.p7 | 21:29043559 | GAACAAGTAAGCACT[C/T]ACAGAAAAAAGCAAA | 10600 |
rs761303399 | snp | A/C | 1.71041e-05 | 0.00292434 | intron-variant | USP16 | GRCh38.p7 | 21:29053764 | CATCTGTGTAAATGG[A/C]ACTAGAACTAACTTT | 10600 |
rs761336476 | snp | A/G | 1.66297e-05 | 0.0028835 | missense | USP16 | GRCh38.p7 | 21:29043508 | AAGAAAAAGATAACG[A/G]CAGTTACATAAAAGA | 10600 |
rs761342296 | snp | C/T | 3.48693e-05 | 0.00417534 | intron-variant | USP16 | GRCh38.p7 | 21:29038306 | GCCTTTAAATAATTT[C/T]TCTCTTTTTTTTTCA | 10600 |
rs761391317 | snp | A/T | 4.98285e-05 | 0.00499117 | utr-variant-3-prime | USP16 | GRCh38.p7 | 21:29054190 | GAGAATACTGTAATA[A/T]TATCAAAAGCACTTT | 10600 |
rs761460283 | snp | A/G/T | 8.50186e-05 | 0.00651947 | intron-variant | USP16 | GRCh38.p7 | 21:29041984 | ATATAACGGTAATTG[A/G/T]TAATTGATAGACTTT | 10600 |
rs761496031 | snp | C/T | 2.03138e-05 | 0.00318693 | intron-variant | USP16 | GRCh38.p7 | 21:29043412 | TTGACCTATGTTATC[C/T]ATATTTTAAGAGTGG | 10600 |
rs761522897 | snp | C/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29049387 | ATGGGCTTGACTAAT[C/T]GGGTGGGCCTTTATT | 10600 |
rs761524767 | in-del | -/GAA | 1.65529e-05 | 0.00287683 | cds-indel | USP16 | GRCh38.p7 | 21:29046975 | ATCTTCTCCCACTAG[-/GAA]TTTAAATGGTGCCTA | 10600 |
rs761579953 | snp | A/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29034614 | GAGCCACCGCGCCTA[A/G]CGAGTGCATGGTTTT | 10600 |
rs761643534 | snp | C/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29049586 | CTTCTTTTTGAAACA[C/G]TCTTGTTCTGTCACC | 10600 |
rs761697005 | snp | G/T | | | intron-variant, upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29026083 | GAGCTTCCAAGATTG[G/T]TAAGATTTAGATAGA | 10600 |
rs761734388 | snp | A/C | 1.65135e-05 | 0.00287341 | missense | USP16 | GRCh38.p7 | 21:29047069 | AATGCTGCTCTTCAT[A/C]CTGATGAAATAAATA | 10600 |
rs761788906 | snp | A/C | 1.6476e-05 | 0.00287014 | missense | USP16 | GRCh38.p7 | 21:29053928 | AATAGTCATCTCTCT[A/C]ATCTTGTTCTTCACG | 10600 |
rs761798701 | snp | A/G | | | upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29024593 | CCGATGGTCCCGGGA[A/G]GTGGGGGTGGGGTGG | 10600 |
rs761830489 | snp | C/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29041143 | GCGCCTGAAATGTGA[C/G]TGGTGAAACTGAGGA | 10600 |
rs761879426 | snp | C/T | 9.93065e-05 | 0.00704581 | missense | USP16 | GRCh38.p7 | 21:29046991 | AATTTAAATGGTGCC[C/T]ACCTAACGGAAGGGA | 10600 |
rs761890770 | snp | A/G | 1.92365e-05 | 0.00310127 | intron-variant | USP16 | GRCh38.p7 | 21:29046645 | TTTCTTTATTTTTTG[A/G]TGCCGTATACTTTTT | 10600 |
rs761984998 | snp | C/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29031830 | ATAATACAGAGAAAT[C/G]CCTATGCATTTTTCT | 10600 |
rs762096245 | snp | A/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29052708 | AGAGTACAGAATAGG[A/T]GAGATGAGAGTTGAA | 10600 |
rs762160759 | snp | A/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29049555 | TGAGAATTTTCTCAC[A/G]AGAAAAGTTGTTTTT | 10600 |
rs762206864 | snp | C/T | 1.67849e-05 | 0.00289692 | intron-variant | USP16 | GRCh38.p7 | 21:29039581 | CAAGTTAGCATGTTA[C/T]GACCATTGTATTTTA | 10600 |
rs762226368 | snp | A/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29044729 | TGGGATTACAGATGT[A/G]AGACACCGTGCCTGG | 10600 |
rs762271372 | snp | C/G | 1.66615e-05 | 0.00288626 | missense | USP16 | GRCh38.p7 | 21:29046737 | GTACTATTGACCATC[C/G]TGAAGACAGTGAATA | 10600 |
rs762294757 | snp | A/G | 1.66131e-05 | 0.00288206 | missense, utr-variant-5-prime | USP16 | GRCh38.p7 | 21:29039482 | TTGTTTTTCTCTAGA[A/G]CAGTGCGGTTTAAAG | 10600 |
rs762403680 | snp | C/T | 0.000396852 | 0.0140808 | utr-variant-5-prime, upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29024683 | ACTCTGGCTTCGACT[C/T]CGTCGCTCTCAATTC | 10600 |
rs762472349 | snp | A/G | 0.000115528 | 0.00759938 | synonymous-codon, utr-variant-5-prime | USP16 | GRCh38.p7 | 21:29039127 | GGGGGTTGTGACACC[A/G]AAAGAACTCTTTTCT | 10600 |
rs762484594 | in-del | -/G | 7.31061e-05 | 0.00604547 | intron-variant | USP16 | GRCh38.p7 | 21:29040692 | AAAGTTAAAGGTAAT[-/G]GTCTGACTTTTTGAA | 10600 |
rs762532602 | snp | A/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29032529 | GAGCCACCGTGCCCA[A/G]CCAGGATTGGCTTTT | 10600 |
rs762574057 | in-del | -/T | 4.00509e-05 | 0.0044748 | intron-variant | USP16 | GRCh38.p7 | 21:29046624 | CCTTTTCTCCCGCTC[-/T]TTCTTTTTCTTTATT | 10600 |
rs762625215 | in-del | -/AA | | | intron-variant | USP16 | GRCh38.p7 | 21:29031321 | TATTACCGTGGTACT[-/AA]AAAGTCAGGGTCTCT | 10600 |
rs762714155 | snp | C/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29047591 | CAGTCACCACAGCAT[C/T]CTGACACATAGTGGC | 10600 |
rs762724265 | snp | A/G | 1.65094e-05 | 0.00287305 | synonymous-codon, utr-variant-5-prime | USP16 | GRCh38.p7 | 21:29038427 | ACCTGATTTGGCATT[A/G]ACAGTATGTTCTTTA | 10600 |
rs762729740 | snp | C/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29035336 | TAAAACAGATTTTTA[C/T]GTCTTAAAAATCATT | 10600 |
rs762745105 | in-del | -/GGATGGT | | | intron-variant | USP16 | GRCh38.p7 | 21:29050666 | CAGCAGTGTAAAATA[-/GGATGGT]GATTGCCAGAGACTG | 10600 |
rs762844792 | snp | C/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29052397 | AGGCAAGGAGGAGCA[C/T]GTCACATCTTACATG | 10600 |
rs762884919 | snp | C/T | 1.65146e-05 | 0.0028735 | missense | USP16 | GRCh38.p7 | 21:29046875 | GCCAAGCAAAAATGA[C/T]CGAAAGTGTAACTGA | 10600 |
rs762945697 | snp | C/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29037833 | TTAAGCCGTCCACCC[C/G]CTTTGGCCACCCAAA | 10600 |
rs763025961 | snp | C/T | 1.86048e-05 | 0.00304993 | intron-variant | USP16 | GRCh38.p7 | 21:29042001 | AATTGATAGACTTTT[C/T]TTTCTCCATAGATTA | 10600 |
rs763051544 | snp | A/G | 1.64795e-05 | 0.00287045 | intron-variant | USP16 | GRCh38.p7 | 21:29054051 | TATGTTTGATTTTTC[A/G]TTTTCTCATGACAGA | 10600 |
rs763127076 | snp | A/G | 1.65999e-05 | 0.00288091 | synonymous-codon | USP16 | GRCh38.p7 | 21:29046750 | TCCTGAAGACAGTGA[A/G]TATGAAGCTGAAATG | 10600 |
rs763133438 | in-del | -/A | 1.64996e-05 | 0.0028722 | frameshift-variant, utr-variant-5-prime | USP16 | GRCh38.p7 | 21:29036275 | TGGGTCACAGGTGTT[-/A]ACGTATGTGATAATG | 10600 |
rs763152114 | snp | A/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29029431 | AAGAAAAAAGAAAAA[A/G]AAGGGTACCTTCTTT | 10600 |
rs763214785 | snp | A/T | 1.648e-05 | 0.0028705 | intron-variant | USP16 | GRCh38.p7 | 21:29053961 | GATATTCCACAAGGT[A/T]AGATGTCTTGGAAAA | 10600 |
rs763234392 | snp | A/G | 1.76412e-05 | 0.0029699 | intron-variant | USP16 | GRCh38.p7 | 21:29048712 | AATCTGAATGCTTTA[A/G]GGGTCTAAAATGATT | 10600 |
rs763358626 | snp | C/T | 1.67351e-05 | 0.00289263 | synonymous-codon, utr-variant-5-prime | USP16 | GRCh38.p7 | 21:29030764 | GCTGTGTCTTAAATG[C/T]GGCCATCAGGTATGC | 10600 |
rs763367489 | snp | A/G | 0.000214683 | 0.0103583 | missense | USP16 | GRCh38.p7 | 21:29048797 | CCAATGCCAAAAAGC[A/G]GATGCTAATTTCTCT | 10600 |
rs763414485 | snp | G/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29046375 | CCAAACTCCTCAAGT[G/T]ATCCTCTTGTGATCA | 10600 |
rs763427202 | snp | A/G | 1.68695e-05 | 0.00290422 | intron-variant | USP16 | GRCh38.p7 | 21:29039586 | TAGCATGTTATGACC[A/G]TTGTATTTTATGATC | 10600 |
rs763522512 | snp | A/G | 5.41218e-05 | 0.00520173 | intron-variant | USP16 | GRCh38.p7 | 21:29030581 | TATTCCTTGTCTATT[A/G]TTTGTTTTAATAGAA | 10600 |
rs763594726 | snp | A/G | | | upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29024464 | CCACACTTCAGGAGC[A/G]TTTATATAACTTCGT | 10600 |
rs763595013 | snp | A/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29032532 | CCACCGTGCCCAGCC[A/G]GGATTGGCTTTTTCA | 10600 |
rs763605225 | in-del | -/TA | | | intron-variant | USP16 | GRCh38.p7 | 21:29047972 | ATGTGTGTGTATGTA[-/TA]TATATATATAAGCTC | 10600 |
rs763637575 | in-del | -/TTTC | 1.98959e-05 | 0.00315398 | intron-variant | USP16 | GRCh38.p7 | 21:29046630 | CTCCCGCTCTTTCTT[-/TTTC]TTTATTTTTTGATGC | 10600 |
rs763668195 | snp | C/T | 3.29853e-05 | 0.00406098 | missense, utr-variant-5-prime | USP16 | GRCh38.p7 | 21:29037395 | CCTCCCATGAATTCT[C/T]CTTGCCAAATAACCG | 10600 |
rs763864315 | snp | A/T | 1.69997e-05 | 0.0029154 | intron-variant | USP16 | GRCh38.p7 | 21:29039599 | CCATTGTATTTTATG[A/T]TCTTATCTTCATAAG | 10600 |
rs763869912 | in-del | -/C | 0.000111412 | 0.00746281 | intron-variant | USP16 | GRCh38.p7 | 21:29041975 | TAATTAATTATATAA[-/C]GGTAATTGGTAATTG | 10600 |
rs763889729 | snp | A/G | 3.43306e-05 | 0.00414296 | intron-variant | USP16 | GRCh38.p7 | 21:29036402 | GTTTCTTTAATATAC[A/G]CCAAATGTCGATTTG | 10600 |
rs763930743 | snp | A/G | 5.12632e-05 | 0.00506251 | missense | USP16 | GRCh38.p7 | 21:29040648 | GCATTTGGTAATTCT[A/G]CTGAAAAGTTGGATG | 10600 |
rs764004566 | snp | A/G | 1.65518e-05 | 0.00287674 | missense | USP16 | GRCh38.p7 | 21:29046977 | CTTCTCCCACTAGGA[A/G]TTTAAATGGTGCCTA | 10600 |
rs764103750 | snp | A/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29044649 | GACAGGTTTCGCCAT[A/G]TTGGTCAGGCTGGTC | 10600 |
rs764105841 | snp | C/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29028438 | GACTTTCTACATCTT[C/T]TTTGTTTTTTTTCCT | 10600 |
rs764145687 | snp | A/G | 1.64773e-05 | 0.00287026 | missense | USP16 | GRCh38.p7 | 21:29054105 | AGTGGTTTCACATCA[A/G]CGACACACATGTGCA | 10600 |
rs764176025 | snp | C/T | 1.64754e-05 | 0.00287009 | synonymous-codon, utr-variant-5-prime | USP16 | GRCh38.p7 | 21:29034929 | TCTTAGTTTGGACAA[C/T]TGGAGTGTATGGTGA | 10600 |
rs764207678 | snp | C/G | 1.71132e-05 | 0.00292511 | intron-variant | USP16 | GRCh38.p7 | 21:29053766 | TCTGTGTAAATGGAA[C/G]TAGAACTAACTTTTG | 10600 |
rs764229077 | snp | C/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29029579 | TGACTAGTTTCTAAA[C/T]CTCCAGTGTTCCTGG | 10600 |
rs764246026 | snp | A/G | 1.67251e-05 | 0.00289176 | missense | USP16 | GRCh38.p7 | 21:29043564 | AGTAAGCACTTACAG[A/G]AAAAAGCAAAGAAAC | 10600 |
rs764263728 | snp | C/T | 1.65888e-05 | 0.00287996 | intron-variant | USP16 | GRCh38.p7 | 21:29034787 | ATTATGCATTCTCCC[C/T]TCTTGCTGAGTTTTT | 10600 |
rs764357450 | snp | A/G | 4.45087e-05 | 0.00471724 | intron-variant, upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29027828 | CTAGAGAAATATAAG[A/G]CATACTTTTTTTTTT | 10600 |
rs764440447 | snp | A/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29051052 | GAATTAACCAGACTT[A/G]ATGATTGATTGGCAC | 10600 |
rs764614636 | snp | C/T | 6.82757e-05 | 0.00584236 | intron-variant | USP16 | GRCh38.p7 | 21:29038978 | TTTTAGTAAAGTCAG[C/T]GATTCCAGAATTTGA | 10600 |
rs764619721 | snp | A/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29043174 | CTAATAAATTTCGTT[A/G]TATTTCTATTACACT | 10600 |
rs764652891 | snp | G/T | 1.99663e-05 | 0.00315955 | intron-variant | USP16 | GRCh38.p7 | 21:29046625 | CTTTTCTCCCGCTCT[G/T]TCTTTTTCTTTATTT | 10600 |
rs764658429 | snp | A/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29039401 | TCTGAGATTTGGGAT[A/T]TGATCCTAAGATTTT | 10600 |
rs764669432 | in-del | -/A | | | upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29024287 | ATTCTGACATGGTGC[-/A]AGGAAGGTAAATTCA | 10600 |
rs764745891 | snp | C/T | | | missense | USP16 | GRCh38.p7 | 21:29048815 | TGCTAATTTCTCTTG[C/T]TCCTCCTGTTCTTAC | 10600 |
rs764806125 | in-del | -/T | 0.00158148 | 0.0280756 | intron-variant | USP16 | GRCh38.p7 | 21:29038311 | TAAATAATTTTTCTC[-/T]TTTTTTTTCACCCTA | 10600 |
rs764881776 | snp | C/T | 6.6464e-05 | 0.00576433 | utr-variant-3-prime | USP16 | GRCh38.p7 | 21:29054191 | AGAATACTGTAATAA[C/T]ATCAAAAGCACTTTT | 10600 |
rs764895912 | in-del | -/G | 1.72006e-05 | 0.00293258 | frameshift-variant | USP16 | GRCh38.p7 | 21:29040659 | TTCTACTGAAAAGTT[-/G]GATGAAGAACTAAAA | 10600 |
rs765023521 | snp | A/T | 1.74601e-05 | 0.00295461 | missense | USP16 | GRCh38.p7 | 21:29040668 | AAAGTTGGATGAAGA[A/T]CTAAAAAATAAAGTT | 10600 |
rs765056861 | snp | C/T | 1.64819e-05 | 0.00287066 | intron-variant | USP16 | GRCh38.p7 | 21:29034948 | AGTGTATGGTGAGTT[C/T]CAGTTCCTCTGCCTC | 10600 |
rs765105406 | snp | C/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29036211 | TCCAGGAATTATTAT[C/T]TGTCTCCCCCTTTTT | 10600 |
rs765239811 | snp | A/C | | | intron-variant | USP16 | GRCh38.p7 | 21:29041815 | CGATTGTGTTCAATT[A/C]TGTTATGCTCAGAGG | 10600 |
rs765259266 | in-del | -/TA | | | intron-variant | USP16 | GRCh38.p7 | 21:29047948 | ATGTGTGTGTATGTA[-/TA]TATATATATATGTGT | 10600 |
rs765287531 | snp | C/T | 9.53898e-05 | 0.00690549 | intron-variant | USP16 | GRCh38.p7 | 21:29046648 | CTTTATTTTTTGATG[C/T]CGTATACTTTTTACC | 10600 |
rs765292425 | snp | A/G | 1.65523e-05 | 0.00287678 | missense | USP16 | GRCh38.p7 | 21:29046992 | ATTTAAATGGTGCCT[A/G]CCTAACGGAAGGGAG | 10600 |
rs765297809 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29026634 | CCGTCCTCCCACCTC[A/G]ATCTCCCAAAGTGTT | 10600 |
rs765307699 | snp | A/G | 1.68216e-05 | 0.00290009 | intron-variant | USP16 | GRCh38.p7 | 21:29053792 | TTTTGGATTCTACTC[A/G]TTTTTAAAGAATGTT | 10600 |
rs765341296 | snp | C/T | 1.66299e-05 | 0.00288352 | synonymous-codon | USP16 | GRCh38.p7 | 21:29046744 | TGACCATCCTGAAGA[C/T]AGTGAATATGAAGCT | 10600 |
rs765364734 | snp | A/C | | | intron-variant | USP16 | GRCh38.p7 | 21:29043164 | CAGCATGTATCTAAT[A/C]AATTTCGTTATATTT | 10600 |
rs765372408 | snp | G/T | 1.65274e-05 | 0.00287462 | missense, utr-variant-5-prime | USP16 | GRCh38.p7 | 21:29039145 | AGAACTCTTTTCTCA[G/T]GTCTGTAAAAAGTGA | 10600 |
rs765471902 | snp | A/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29028234 | TCAAACGGTTCTCTC[A/G]TGCCTCAGCCTCTGA | 10600 |
rs765516642 | snp | A/G | 0.000100614 | 0.00709202 | intron-variant | USP16 | GRCh38.p7 | 21:29050181 | CCTTAAATGTAAGGT[A/G]AGTCAAAGTGGTCTT | 10600 |
rs765561459 | snp | A/G/T | 5.87232e-05 | 0.00541837 | intron-variant | USP16 | GRCh38.p7 | 21:29047364 | AATTAATATTCAGGG[A/G/T]CACATTTTGCACTGC | 10600 |
rs765600675 | snp | G/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29038606 | GGCATTACATCTGTT[G/T]GCTGTGTGTGTGCTC | 10600 |
rs765653234 | snp | A/G/T | 0.000115574 | 0.00760099 | missense | USP16 | GRCh38.p7 | 21:29047235 | TATATCAGTTCACCC[A/G/T]TAATGAGAAACTTCG | 10600 |
rs765698785 | snp | A/G | 1.6945e-05 | 0.00291071 | missense, utr-variant-5-prime | USP16 | GRCh38.p7 | 21:29027968 | GATGATTCCTCTGAA[A/G]CTTTAGGTATATTTC | 10600 |
rs765786674 | snp | C/T | 1.66032e-05 | 0.0028812 | missense, utr-variant-5-prime | USP16 | GRCh38.p7 | 21:29039483 | TGTTTTTCTCTAGAG[C/T]AGTGCGGTTTAAAGG | 10600 |
rs765786858 | snp | C/G | 1.91893e-05 | 0.00309746 | intron-variant, upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29027855 | TTTTGGTCAAGCTAA[C/G]TTTATCTTGTTTTCT | 10600 |
rs765888688 | snp | C/G | 0.000559858 | 0.0167217 | utr-variant-5-prime, upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29024720 | AGGAGGAAGACGGAG[C/G]TGGCTGCCCAGCCCA | 10600 |
rs765979165 | snp | A/G | 1.66546e-05 | 0.00288566 | utr-variant-3-prime | USP16 | GRCh38.p7 | 21:29054198 | TGTAATAATATCAAA[A/G]GCACTTTTTCTGGAA | 10600 |
rs765981729 | snp | A/C | 1.65064e-05 | 0.00287279 | synonymous-codon | USP16 | GRCh38.p7 | 21:29047086 | TGATGAAATAAATAT[A/C]GAGATTCTGAATGAT | 10600 |
rs766015231 | snp | A/T | 1.64942e-05 | 0.00287173 | missense, utr-variant-5-prime | USP16 | GRCh38.p7 | 21:29039108 | AGATGCAAGAGACCA[A/T]AAAGGGGGTTGTGAC | 10600 |
rs766049950 | snp | C/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29053724 | TAAAGACCCTTTGCA[C/T]AGTGTAAACTTGTCT | 10600 |
rs766085811 | in-del | -/GC | | | intron-variant | USP16 | GRCh38.p7 | 21:29043792 | TGAAGAAAACGTCGT[-/GC]TTCTTTTTTTTTAAA | 10600 |
rs766140631 | in-del | -/AG | | | intron-variant | USP16 | GRCh38.p7 | 21:29031847 | CTATGCATTTTTCTC[-/AG]AGTCCCCCAGTGGTA | 10600 |
rs766206100 | snp | A/G | 1.65091e-05 | 0.00287303 | synonymous-codon | USP16 | GRCh38.p7 | 21:29053825 | AGAAGAAAATACAAG[A/G]GTACTCTATTCCTTA | 10600 |
rs766209096 | snp | C/G | | | intron-variant, upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29026315 | ACAAAAATTAGCCGG[C/G]TGTGGTGGTGGGCGT | 10600 |
rs766280844 | snp | A/C | 6.64982e-05 | 0.00576582 | missense, utr-variant-5-prime | USP16 | GRCh38.p7 | 21:29036368 | AGCATTACAACTCCA[A/C]AGCCAGGTAAAATAA | 10600 |
rs766337207 | snp | A/C | | | intron-variant | USP16 | GRCh38.p7 | 21:29049697 | CTATAGTAGCTGGGA[A/C]TATAGGTGGCTACCA | 10600 |
rs766345858 | snp | G/T | 1.73333e-05 | 0.00294386 | intron-variant | USP16 | GRCh38.p7 | 21:29027981 | AAACTTTAGGTATAT[G/T]TCATTGATTGAATCT | 10600 |
rs766368554 | snp | A/G | 1.6596e-05 | 0.00288058 | intron-variant | USP16 | GRCh38.p7 | 21:29034984 | TGGAAATTATTTGAA[A/G]TATTAGAGAATGGAA | 10600 |
rs766379118 | snp | A/G | 1.70015e-05 | 0.00291555 | missense | USP16 | GRCh38.p7 | 21:29042091 | GTATGATCATGTGTG[A/G]TCAATGCAGAACTGT | 10600 |
rs766407223 | snp | A/C | | | intron-variant | USP16 | GRCh38.p7 | 21:29039746 | AGAATGAATCCAGAG[A/C]ATTAGCAGTAATTCT | 10600 |
rs766433691 | snp | A/G | 4.96792e-05 | 0.00498368 | missense, utr-variant-5-prime | USP16 | GRCh38.p7 | 21:29039489 | TCTCTAGAGCAGTGC[A/G]GTTTAAAGGCTATCA | 10600 |
rs766459264 | snp | C/T | 1.68764e-05 | 0.00290481 | intron-variant | USP16 | GRCh38.p7 | 21:29039587 | AGCATGTTATGACCA[C/T]TGTATTTTATGATCT | 10600 |
rs766523511 | snp | C/T | 9.95801e-05 | 0.0070555 | missense | USP16 | GRCh38.p7 | 21:29046751 | CCTGAAGACAGTGAA[C/T]ATGAAGCTGAAATGT | 10600 |
rs766593363 | snp | A/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29030021 | TATTATTATCTTCTA[A/G]GATTGCACAGATGTT | 10600 |
rs766611240 | snp | G/T | 1.648e-05 | 0.0028705 | intron-variant | USP16 | GRCh38.p7 | 21:29053965 | TTCCACAAGGTAAGA[G/T]GTCTTGGAAAATTCA | 10600 |
rs766695040 | in-del | -/A | 1.64914e-05 | 0.00287149 | frameshift-variant | USP16 | GRCh38.p7 | 21:29054145 | TACAACTAAAGTACT[-/A]AACTCACAAGCGTAC | 10600 |
rs766709778 | snp | A/G | 2.01977e-05 | 0.00317781 | intron-variant | USP16 | GRCh38.p7 | 21:29043413 | TGACCTATGTTATCT[A/G]TATTTTAAGAGTGGT | 10600 |
rs766724300 | snp | A/G | 1.65151e-05 | 0.00287355 | missense | USP16 | GRCh38.p7 | 21:29048801 | TGCCAAAAAGCAGAT[A/G]CTAATTTCTCTTGCT | 10600 |
rs766729662 | snp | C/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29025162 | TAGGAAAAGCAGGAT[C/T]TGTCACTTATCCAAT | 10600 |
rs766788634 | snp | A/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29046597 | TGTCCTTCTTCCTCT[A/G]TCTCTCTTCCTCCTT | 10600 |
rs766833090 | snp | A/C | | | intron-variant | USP16 | GRCh38.p7 | 21:29031932 | CACACCAATCGCAAT[A/C]AGATCTCCTGAGTTT | 10600 |
rs766853755 | snp | A/C | 1.75001e-05 | 0.002958 | intron-variant | USP16 | GRCh38.p7 | 21:29048720 | TGCTTTAGGGGTCTA[A/C]AATGATTTTCTCCCT | 10600 |
rs766867815 | snp | A/T | 1.69594e-05 | 0.00291194 | missense, utr-variant-5-prime | USP16 | GRCh38.p7 | 21:29030603 | TTAATAGAACCTGTG[A/T]GCAGACACATTAGAA | 10600 |
rs766905054 | snp | C/T | 1.65345e-05 | 0.00287524 | intron-variant | USP16 | GRCh38.p7 | 21:29042459 | TTTACACTGTCTTTT[C/T]TGATTGGTTAAGGTC | 10600 |
rs766905980 | in-del | -/A | 5.31439e-05 | 0.00515452 | intron-variant | USP16 | GRCh38.p7 | 21:29047329 | TATAAAAGGTATTTT[-/A]ATGCTCTCACTGTAA | 10600 |
rs767012930 | snp | G/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29035675 | GGCATGAGCCACCGT[G/T]CCTGGCTTGAATGGC | 10600 |
rs767041543 | snp | A/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29047716 | AGACAGTGCTTTCTT[A/T]CAGTCTTCCTCAAAT | 10600 |
rs767097319 | snp | A/C | 1.64974e-05 | 0.00287201 | missense | USP16 | GRCh38.p7 | 21:29047106 | TTCTGAATGATAGTC[A/C]TACTCCTGGAACAAA | 10600 |
rs767116610 | snp | C/T | 1.70589e-05 | 0.00292047 | intron-variant | USP16 | GRCh38.p7 | 21:29036397 | AATTTGTTTCTTTAA[C/T]ATACACCAAATGTCG | 10600 |
rs767131433 | snp | C/T | 1.65097e-05 | 0.00287308 | missense | USP16 | GRCh38.p7 | 21:29047232 | GTTTATATCAGTTCA[C/T]CCGTAATGAGAAACT | 10600 |
rs767207094 | in-del | -/AT | 1.64789e-05 | 0.0028704 | frameshift-variant | USP16 | GRCh38.p7 | 21:29054114 | ACATCAGCGACACAC[-/AT]GTGCAAGCTGTGCCT | 10600 |
rs767301772 | snp | A/G | 1.64817e-05 | 0.00287064 | intron-variant | USP16 | GRCh38.p7 | 21:29053984 | TTGGAAAATTCAGGC[A/G]CTCAGCAGATTACGG | 10600 |
rs767315337 | snp | A/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29050855 | TTAAAGCACTGGGGT[A/G]GCATGGTCAGATCTT | 10600 |
rs767364280 | snp | C/T | | | upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29023217 | GCTGAGGTCGTGCCA[C/T]TGCACTCCAGCCTGG | 10600 |
rs767501915 | snp | A/G | 1.67744e-05 | 0.00289602 | missense, utr-variant-5-prime | USP16 | GRCh38.p7 | 21:29030610 | AACCTGTGTGCAGAC[A/G]CATTAGAAAAGGATT | 10600 |
rs767525601 | snp | A/C | 1.64947e-05 | 0.00287177 | missense, utr-variant-5-prime | USP16 | GRCh38.p7 | 21:29037378 | ACATGGCTAAAGAGA[A/C]TCCTCCCATGAATTC | 10600 |
rs767546967 | snp | C/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29052739 | TAAATAGAAGACTTG[C/T]GGACTAAGACTAAAA | 10600 |
rs767678384 | snp | C/G | 3.37752e-05 | 0.00410932 | intron-variant | USP16 | GRCh38.p7 | 21:29039589 | CATGTTATGACCATT[C/G]TATTTTATGATCTTA | 10600 |
rs767751492 | snp | G/T | 1.65162e-05 | 0.00287365 | splice-donor-variant | USP16 | GRCh38.p7 | 21:29038431 | GATTTGGCATTAACA[G/T]TATGTTCTTTAAACT | 10600 |
rs767828672 | snp | C/T | 1.6612e-05 | 0.00288196 | synonymous-codon | USP16 | GRCh38.p7 | 21:29043542 | AAGTGATATTCCTTC[C/T]GGAACAAGTAAGCAC | 10600 |
rs767830335 | in-del | -/TTAAA | 1.65512e-05 | 0.00287669 | frameshift-variant | USP16 | GRCh38.p7 | 21:29046979 | TCTCCCACTAGGAAT[-/TTAAA]TGGTGCCTACCTAAC | 10600 |
rs767968130 | snp | C/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29044736 | ACAGATGTGAGACAC[C/T]GTGCCTGGCCCATTC | 10600 |
rs767992513 | snp | C/G | 8.3273e-05 | 0.0064521 | intron-variant | USP16 | GRCh38.p7 | 21:29038324 | TCTTTTTTTTTCACC[C/G]TACATTCTAGAACTT | 10600 |
rs768002703 | snp | A/T | 1.81651e-05 | 0.00301368 | missense | USP16 | GRCh38.p7 | 21:29043434 | TAAGAGTGGTAAGAA[A/T]AGTGTAAATGATAAA | 10600 |
rs768071962 | snp | C/T | 4.97459e-05 | 0.00498703 | missense | USP16 | GRCh38.p7 | 21:29050107 | GCTGGTTTTAACCTA[C/T]GCAAAGTTAACAAAC | 10600 |
rs768092996 | snp | C/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29029824 | AAGTCTGAAAGACTT[C/G]AGTCTAAATTCTGGC | 10600 |
rs768119709 | in-del | -/T | 1.64792e-05 | 0.00287042 | intron-variant | USP16 | GRCh38.p7 | 21:29054044 | TCCATTTATGTTTGA[-/T]TTTTTCATTTTCTCA | 10600 |
rs768162071 | snp | C/G | 1.65274e-05 | 0.00287462 | missense | USP16 | GRCh38.p7 | 21:29048830 | CTCCTCCTGTTCTTA[C/G]TCTTCATTTAAAGAG | 10600 |
rs768234668 | snp | A/G | 1.65173e-05 | 0.00287374 | missense | USP16 | GRCh38.p7 | 21:29048794 | ACACCAATGCCAAAA[A/G]GCAGATGCTAATTTC | 10600 |
rs768301793 | snp | C/G | 6.60644e-05 | 0.00574698 | missense | USP16 | GRCh38.p7 | 21:29047060 | CTAAATTTGAATGCT[C/G]CTCTTCATCCTGATG | 10600 |
rs768302634 | snp | A/G | 1.64743e-05 | 0.00287 | synonymous-codon, utr-variant-5-prime | USP16 | GRCh38.p7 | 21:29034860 | CAGAAATTCTCAGGA[A/G]CAGCATGCCTTGAAG | 10600 |
rs768402394 | snp | A/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29032749 | ACAGGTTTTTGTGTG[A/G]ACTTAGATTTCATTT | 10600 |
rs768462448 | snp | A/G | 1.66236e-05 | 0.00288297 | synonymous-codon, utr-variant-5-prime | USP16 | GRCh38.p7 | 21:29030752 | GCCTTCAGTTTGGCT[A/G]TGTCTTAAATGTGGC | 10600 |
rs768535695 | snp | A/G | 1.79194e-05 | 0.00299322 | intron-variant | USP16 | GRCh38.p7 | 21:29043622 | ATTAGGAGGAAAATC[A/G]TATGCTTGTAATTTT | 10600 |
rs768595655 | snp | A/C | 1.6492e-05 | 0.00287154 | synonymous-codon, utr-variant-5-prime | USP16 | GRCh38.p7 | 21:29038391 | AGTGAAAATGTCTGG[A/C]ACAATTGTAAAAATT | 10600 |
rs768616674 | snp | C/T | 1.84242e-05 | 0.00303509 | intron-variant | USP16 | GRCh38.p7 | 21:29042139 | ACTGGGTTTATTTGC[C/T]AATATTCAACAGTTT | 10600 |
rs768705409 | snp | A/G | 1.64773e-05 | 0.00287026 | missense, utr-variant-5-prime | USP16 | GRCh38.p7 | 21:29036326 | AACCAGTTGGGTCAA[A/G]TGGTTGATTATGTCA | 10600 |
rs768708340 | snp | C/T | 2.23501e-05 | 0.00334284 | intron-variant | USP16 | GRCh38.p7 | 21:29041975 | TAATTAATTATATAA[C/T]GGTAATTGGTAATTG | 10600 |
rs768754865 | in-del | -/ACTG | | | intron-variant | USP16 | GRCh38.p7 | 21:29041844 | GGTGGAATATATAAT[-/ACTG]ACTTCTATTGCTTAA | 10600 |
rs768798142 | snp | C/T | 1.67964e-05 | 0.00289792 | missense | USP16 | GRCh38.p7 | 21:29042070 | TCTTTGGTGGTGAAC[C/T]AACTAGTATGATCAT | 10600 |
rs768844526 | snp | A/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29031595 | GGTGTGTGCCACCAC[A/G]CCTGGCTGAGTTTTG | 10600 |
rs768851173 | snp | C/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29046071 | TCAAGTGAGATGCCC[C/T]CCTTGGCCTCCCAAA | 10600 |
rs768883111 | in-del | -/T | 1.65141e-05 | 0.00287346 | frameshift-variant, utr-variant-5-prime | USP16 | GRCh38.p7 | 21:29039136 | ACACCGAAAGAACTC[-/T]TTTTCTCAGGTCTGT | 10600 |
rs768886025 | snp | A/C | 1.64825e-05 | 0.00287071 | missense | USP16 | GRCh38.p7 | 21:29047181 | CTCTTGCAAACAGGG[A/C]AGTTTTCAATACTGA | 10600 |
rs768961885 | snp | A/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29036819 | TTTGCTTTAAGCATG[A/T]TTTTTAAGTTTTTAT | 10600 |
rs768996685 | in-del | -/AGAAGAAAC | | | cds-indel | USP16 | GRCh38.p7 | 21:29030719 | GAAAGATAAAGCTGA[-/AGAAGAAAC]AGAAGAAAAGCCTTC | 10600 |
rs769000223 | snp | A/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29035788 | GCTGGGCATGGTGGT[A/G]GGTGCCTGTAGTCCC | 10600 |
rs769022247 | snp | C/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29049442 | GCATGAGGCTGAGAG[C/T]GTGTGTTTCACAGAA | 10600 |
rs769076062 | snp | C/T | 1.64789e-05 | 0.0028704 | intron-variant | USP16 | GRCh38.p7 | 21:29054028 | TAATCAACTTGAATC[C/T]TTCCATTTATGTTTG | 10600 |
rs769134327 | snp | A/G | 1.65141e-05 | 0.00287346 | missense | USP16 | GRCh38.p7 | 21:29046824 | AAGAGGGTGTTATGC[A/G]TAAAGAATATTGTGT | 10600 |
rs769188157 | snp | C/T | 1.65285e-05 | 0.00287471 | intron-variant | USP16 | GRCh38.p7 | 21:29037246 | TATGACTGTATTACA[C/T]ATTTTGCTAAATCTT | 10600 |
rs769201232 | snp | C/T | 1.89414e-05 | 0.00307739 | intron-variant | USP16 | GRCh38.p7 | 21:29043644 | TGTAATTTTATATTT[C/T]GAGCTATTGAGTTTG | 10600 |
rs769242258 | snp | A/C | | | intron-variant | USP16 | GRCh38.p7 | 21:29038833 | ATAATCTAAAACTAA[A/C]ATAGTAGAGCTGAAT | 10600 |
rs769293043 | snp | C/T | 1.79248e-05 | 0.00299368 | intron-variant | USP16 | GRCh38.p7 | 21:29050224 | CCTTTAAAGTCAAAT[C/T]GTGGCTTACCTAATG | 10600 |
rs769402341 | snp | C/T | | | upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29024299 | GTGCAGGAAGGTAAA[C/T]TCAAGACAACTTAGG | 10600 |
rs769411728 | snp | C/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29029220 | AGATCGAGACCATCC[C/T]GGCTAACACGGTGAA | 10600 |
rs769450062 | snp | C/T | 1.66288e-05 | 0.00288343 | synonymous-codon | USP16 | GRCh38.p7 | 21:29043509 | AGAAAAAGATAACGA[C/T]AGTTACATAAAAGAG | 10600 |
rs769512859 | snp | C/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29046041 | GTTGGCCAGGCTGGT[C/T]TCAAACTCCTCACCT | 10600 |
rs769662343 | in-del | -/G | 1.69648e-05 | 0.00291241 | intron-variant | USP16 | GRCh38.p7 | 21:29050191 | AAGGTAAGTCAAAGT[-/G]GTCTTTTTCAGGAAA | 10600 |
rs769693119 | snp | A/C | | | intron-variant | USP16 | GRCh38.p7 | 21:29031345 | GGTCTCTCAGTTACC[A/C]TTAGTGGTGGCAAGT | 10600 |
rs769758073 | snp | A/G | 1.65386e-05 | 0.00287559 | missense, utr-variant-5-prime | USP16 | GRCh38.p7 | 21:29037431 | GGACTCAGTAATTTG[A/G]GAAACACATGTTTCT | 10600 |
rs769760836 | snp | A/G | 0.000189915 | 0.00974278 | utr-variant-5-prime, upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29024644 | ATAATGCCGCGTTCC[A/G]GAAGTTATTGCTTTC | 10600 |
rs769764591 | snp | C/G | 1.66707e-05 | 0.00288705 | intron-variant | USP16 | GRCh38.p7 | 21:29039189 | TTGTGCTTTCAGTGC[C/G]TCAGTGAGATGCTGA | 10600 |
rs769773454 | snp | C/T | 1.64866e-05 | 0.00287106 | missense | USP16 | GRCh38.p7 | 21:29047193 | GGGAAGTTTTCAATA[C/T]TGATGAGTGTTCAAT | 10600 |
rs769817780 | in-del | -/A | 3.3227e-05 | 0.00407583 | intron-variant | USP16 | GRCh38.p7 | 21:29034988 | ATTATTTGAAATATT[-/A]AGAGAATGGAAATGT | 10600 |
rs769857355 | in-del | -/T | 0.00023896 | 0.0109281 | intron-variant | USP16 | GRCh38.p7 | 21:29043633 | ATCATATGCTTGTAA[-/T]TTTTATATTTTGAGC | 10600 |
rs769903622 | in-del | -/TG | 0.00039004 | 0.0139595 | intron-variant | USP16 | GRCh38.p7 | 21:29038475 | ACTTTCCTCTCTGAA[-/TG]TGTGTTTTCTAAATT | 10600 |
rs769929207 | snp | A/G | 3.76634e-05 | 0.00433939 | intron-variant, splice-acceptor-variant | USP16 | GRCh38.p7 | 21:29037275 | TTTTCTTTTTTTAAA[A/G]CAGAGAAAGATAATG | 10600 |
rs769977275 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29027506 | AGGGAAGCAAATCAG[C/T]TTTCTGATTAAAGTG | 10600 |
rs769986465 | snp | C/G | 1.6476e-05 | 0.00287014 | missense | USP16 | GRCh38.p7 | 21:29053931 | AGTCATCTCTCTAAT[C/G]TTGTTCTTCACGGTG | 10600 |
rs770093540 | snp | A/G | 3.81047e-05 | 0.00436473 | intron-variant | USP16 | GRCh38.p7 | 21:29042150 | TTGCTAATATTCAAC[A/G]GTTTATCAATTGTTT | 10600 |
rs770124908 | snp | C/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29050565 | TAAAGTAAACCATGC[C/T]TCAACTATATTTAAA | 10600 |
rs770209399 | snp | A/T | 3.3083e-05 | 0.00406699 | missense | USP16 | GRCh38.p7 | 21:29046938 | AAAATATCAACATGG[A/T]TAATGATCTGGAGGT | 10600 |
rs770266885 | snp | C/T | 1.86107e-05 | 0.00305041 | intron-variant | USP16 | GRCh38.p7 | 21:29030573 | ACCTTATATATTCCT[C/T]GTCTATTATTTGTTT | 10600 |
rs770285384 | snp | A/G | 1.68018e-05 | 0.00289838 | intron-variant | USP16 | GRCh38.p7 | 21:29039582 | AAGTTAGCATGTTAT[A/G]ACCATTGTATTTTAT | 10600 |
rs770352746 | snp | C/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29034553 | CCTGACCTCAGGTGA[C/T]CCCACCCCTGGCCTC | 10600 |
rs770362341 | snp | A/T | 1.75136e-05 | 0.00295914 | intron-variant | USP16 | GRCh38.p7 | 21:29039450 | CTTAGTAGACTGAAG[A/T]TTGCTTTTCTGTCTT | 10600 |
rs770387387 | snp | C/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29046122 | AGCCACCACACCTGG[C/T]CTAAATAACTTTTCT | 10600 |
rs770406045 | snp | A/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29035608 | CAAACTCCTGACCTC[A/G]TGATCCCCTTGTGAT | 10600 |
rs770424849 | snp | A/G | 1.66963e-05 | 0.00288927 | missense, upstream-variant-2KB, utr-variant-5-prime | USP16 | GRCh38.p7 | 21:29027944 | ACAAAGGGAAAAACT[A/G]TTCCAATCGATGATT | 10600 |
rs770439973 | snp | A/C | 1.70484e-05 | 0.00291957 | missense | USP16 | GRCh38.p7 | 21:29046698 | AAAAAATTCAAGGAA[A/C]AGTTCTTCATTTAAA | 10600 |
rs770473131 | snp | A/G | 1.65124e-05 | 0.00287331 | missense, utr-variant-5-prime | USP16 | GRCh38.p7 | 21:29039534 | AGGAGCTGCTTCGCT[A/G]CTTATTGGATGGGAT | 10600 |
rs770536841 | in-del | -/C | | | intron-variant | USP16 | GRCh38.p7 | 21:29042388 | AACCCATCCCCTACT[-/C]CCCATCCCACAGGGC | 10600 |
rs770547691 | snp | A/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29037149 | TCTATTTAAAATCAA[A/G]TGGGTGGGTGGGTTG | 10600 |
rs770564697 | snp | C/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29042973 | ACTTCATATGAATTA[C/T]GAGACCCTTGGCTTG | 10600 |
rs770590301 | snp | C/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29044807 | ATTCTGTGTTATGGA[C/T]GTGCCATAATTCATT | 10600 |
rs770644386 | snp | A/T | 1.65312e-05 | 0.00287495 | missense | USP16 | GRCh38.p7 | 21:29048779 | AAAGGAAGCATGTTT[A/T]CACCAATGCCAAAAA | 10600 |
rs770695277 | in-del | -/A | 1.67198e-05 | 0.0028913 | frameshift-variant | USP16 | GRCh38.p7 | 21:29043563 | AGTAAGCACTTACAG[-/A]AAAAAAGCAAAGAAA | 10600 |
rs770732807 | in-del | -/ATCTT | 1.6995e-05 | 0.00291499 | intron-variant | USP16 | GRCh38.p7 | 21:29039599 | CCATTGTATTTTATG[-/ATCTT]ATCTTCATAAGCTTT | 10600 |
rs770816497 | snp | C/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29044070 | CCTGAGCAGTCAGGA[C/T]TACAGGTGCATGCCA | 10600 |
rs770837377 | snp | A/G | 8.27835e-05 | 0.00643311 | missense, utr-variant-5-prime | USP16 | GRCh38.p7 | 21:29037350 | AATGAACAAGAGAGA[A/G]AAAAGAAGGAAAACA | 10600 |
rs770843640 | snp | C/G | 1.67041e-05 | 0.00288994 | intron-variant | USP16 | GRCh38.p7 | 21:29042571 | AGTAGATTTTTTTTC[C/G]TGTAAGATTTTGTGG | 10600 |
rs770904745 | snp | A/C | 0.000133945 | 0.00818258 | utr-variant-5-prime, upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29027909 | GTAATCCATAAAGTG[A/C]CAACATGGGAAAGAA | 10600 |
rs770909224 | snp | A/T | 1.65485e-05 | 0.00287645 | intron-variant | USP16 | GRCh38.p7 | 21:29028021 | ATATCTCTAAATGAA[A/T]ATGTTTTAAAATGTA | 10600 |
rs770968529 | snp | A/G | 3.30945e-05 | 0.0040677 | synonymous-codon | USP16 | GRCh38.p7 | 21:29046957 | TGATCTGGAGGTTTT[A/G]ACATCTTCTCCCACT | 10600 |
rs771023528 | in-del | -/TT/TTTT/TTTTT | | | intron-variant, upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29026537 | CATCTGCATTTTACC[-/TT/TTTT/TTTTT]TTTTTTTTTTTTTTT | 10600 |
rs771058649 | snp | C/T | 1.6495e-05 | 0.0028718 | synonymous-codon | USP16 | GRCh38.p7 | 21:29054148 | AACTAAAGTACTAAA[C/T]TCACAAGCGTACCTC | 10600 |
rs771092778 | snp | A/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29034474 | TGCGCCACCACACCC[A/G]GCTAATTTTTGTATT | 10600 |
rs771212495 | snp | A/G | 1.67604e-05 | 0.00289481 | missense, utr-variant-5-prime | USP16 | GRCh38.p7 | 21:29030766 | TGTGTCTTAAATGTG[A/G]CCATCAGGTATGCTT | 10600 |
rs771248987 | snp | C/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29025612 | AGTTTTCCTATGGAG[C/T]CTAAGCTGCTGCAAT | 10600 |
rs771302505 | snp | C/G | 1.74747e-05 | 0.00295585 | missense | USP16 | GRCh38.p7 | 21:29040621 | TAGAGAGTGAGTAAA[C/G]GAATACTTAAAGCAT | 10600 |
rs771304945 | snp | G/T | 1.68015e-05 | 0.00289836 | intron-variant | USP16 | GRCh38.p7 | 21:29050081 | GTCAATCTGTTATGC[G/T]TCTCTTTTAGGCTGG | 10600 |
rs771323198 | snp | G/T | 1.64738e-05 | 0.00286995 | missense, utr-variant-5-prime | USP16 | GRCh38.p7 | 21:29034872 | GGAGCAGCATGCCTT[G/T]AAGCACTATCTGACG | 10600 |
rs771331303 | snp | A/G | 3.85572e-05 | 0.00439057 | intron-variant | USP16 | GRCh38.p7 | 21:29040720 | GAACTAAAACACTAT[A/G]GTTGAATTCCTCTGT | 10600 |
rs771353590 | in-del | -/A | 1.72249e-05 | 0.00293465 | intron-variant | USP16 | GRCh38.p7 | 21:29030797 | CGTTTTAAGATCAAT[-/A]ATGGGATTTTAGAAA | 10600 |
rs771377468 | snp | A/G | 1.65441e-05 | 0.00287607 | synonymous-codon | USP16 | GRCh38.p7 | 21:29047020 | GAGCAATGGAGAAGT[A/G]GACATTTCCAATGGT | 10600 |
rs771489383 | snp | A/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29047575 | TTATCCCCTTGGAAT[A/G]CAGTCACCACAGCAT | 10600 |
rs771492628 | snp | C/T | 1.9562e-05 | 0.0031274 | intron-variant | USP16 | GRCh38.p7 | 21:29030549 | ATTAACTGAAGAAAG[C/T]CATTTTTGACCTTAT | 10600 |
rs771535036 | snp | C/G | 1.65195e-05 | 0.00287393 | missense | USP16 | GRCh38.p7 | 21:29048788 | ATGTTTACACCAATG[C/G]CAAAAAGCAGATGCT | 10600 |
rs771538443 | snp | A/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29033138 | GAATATATTTTGTGT[A/T]ACAAATTTTTGTGCT | 10600 |
rs771540658 | snp | A/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29048936 | TTACTGTCTCAACAT[A/T]CTACTTTGTTTCTTT | 10600 |
rs771605306 | snp | A/G | 1.64825e-05 | 0.00287071 | missense, utr-variant-5-prime | USP16 | GRCh38.p7 | 21:29030693 | CAAGACTGTAAGACT[A/G]ACAATAAAGTGAAAG | 10600 |
rs771627125 | snp | C/G | 1.83714e-05 | 0.00303073 | intron-variant | USP16 | GRCh38.p7 | 21:29047341 | TTTAATGCTCTCACT[C/G]TAAGTAAAATTAATA | 10600 |
rs771667412 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29027310 | TCATTTAGCTGATAC[A/G]CATAGGAAATCCTGG | 10600 |
rs771720615 | snp | A/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29028843 | ATTTAGGTAATCTTT[A/G]ACTTTTTAGTATTAT | 10600 |
rs771737301 | snp | C/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29050692 | GCCAGAGACTGGTAA[C/T]GTATGTAGTTCTAGA | 10600 |
rs771741706 | snp | A/G | 8.25771e-05 | 0.00642508 | synonymous-codon | USP16 | GRCh38.p7 | 21:29054157 | ACTAAACTCACAAGC[A/G]TACCTCCTATTTTAT | 10600 |
rs771762471 | snp | A/G | 1.64925e-05 | 0.00287158 | missense, utr-variant-5-prime | USP16 | GRCh38.p7 | 21:29038371 | CTTAGAGAACTACTA[A/G]AAGAAGTGAAAATGT | 10600 |
rs771764513 | snp | A/G | 1.67103e-05 | 0.00289048 | missense | USP16 | GRCh38.p7 | 21:29043484 | AGGATGAAGATCAAG[A/G]TAGTGAGGAAGAAAA | 10600 |
rs771806251 | snp | C/T | 3.33528e-05 | 0.00408354 | intron-variant | USP16 | GRCh38.p7 | 21:29039571 | AGAAGAACACCAAGT[C/T]AGCATGTTATGACCA | 10600 |
rs771826207 | snp | A/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29041564 | CTTAGAGTTCACAAA[A/G]CAAGTTACATGCATT | 10600 |
rs771923450 | in-del | -/AG | 0.000100869 | 0.00710101 | frameshift-variant, utr-variant-5-prime | USP16 | GRCh38.p7 | 21:29037325 | TAAAAAATTAGAAAA[-/AG]AGAGTAAGAATGAAC | 10600 |
rs771945791 | snp | C/G | 1.71631e-05 | 0.00292938 | intron-variant | USP16 | GRCh38.p7 | 21:29048896 | TTTAAATATGTAACA[C/G]CTACTTTATTACCTA | 10600 |
rs771993825 | snp | C/T | 2.23307e-05 | 0.00334138 | intron-variant | USP16 | GRCh38.p7 | 21:29043394 | AGTTGTAAAATTTTG[C/T]TTTTGACCTATGTTA | 10600 |
rs772061642 | snp | C/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29041193 | TTAATTGTAATTAAA[C/T]TTAAATAGCCGTAAG | 10600 |
rs772131909 | snp | C/G | 2.0179e-05 | 0.00317633 | intron-variant | USP16 | GRCh38.p7 | 21:29040732 | TATAGTTGAATTCCT[C/G]TGTACCTTAGGACAA | 10600 |
rs772276412 | in-del | -/TTT | | | intron-variant | USP16 | GRCh38.p7 | 21:29037588 | AGAAAACTTTTTTTT[-/TTT]TTTTTTTTTTTTTTG | 10600 |
rs772334419 | snp | A/G | | | upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29023928 | TTTCAAAGAATGGAC[A/G]GTAAATATTTGAAAA | 10600 |
rs772340250 | snp | A/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29049623 | GGTGTGCAATGACAC[A/G]ATCATGGCTCACTGA | 10600 |
rs772396946 | snp | C/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29052564 | TACCCTCCCATGACA[C/T]GTGGGAATTGTGGGA | 10600 |
rs772451518 | snp | A/C/G | 0.000303582 | 0.0123168 | intron-variant | USP16 | GRCh38.p7 | 21:29046620 | TCCTCCTTTTCTCCC[A/C/G]CTCTTTCTTTTTCTT | 10600 |
rs772452307 | snp | A/G | 1.64784e-05 | 0.00287035 | missense, utr-variant-5-prime | USP16 | GRCh38.p7 | 21:29036305 | GAGGTCCAGTATTGT[A/G]GTTCAAACCAGTTGG | 10600 |
rs772505025 | snp | C/T | | | upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29023483 | TAGCTATCTGCAACT[C/T]CCCCGACCCCCACGG | 10600 |
rs772534284 | snp | A/C | 1.64738e-05 | 0.00286995 | missense | USP16 | GRCh38.p7 | 21:29053886 | AGGTCGGGGCATTAC[A/C]CTGCCTATGCCAAGG | 10600 |
rs772613184 | snp | C/T | 1.64746e-05 | 0.00287002 | missense | USP16 | GRCh38.p7 | 21:29042051 | CCAAGTTTTGTTGAC[C/T]GCATCTTTGGTGGTG | 10600 |
rs772729913 | snp | G/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29051971 | TGTTTCTTGGCAGTA[G/T]TGGCCATCTGGGTTT | 10600 |
rs772754854 | snp | A/C | | | intron-variant | USP16 | GRCh38.p7 | 21:29035860 | GGAGCTGGAGGTTGC[A/C]GTGAGCCGAGATCCT | 10600 |
rs772758055 | snp | C/G | 6.59642e-05 | 0.00574262 | missense, utr-variant-5-prime | USP16 | GRCh38.p7 | 21:29039101 | CTTAATGAGATGCAA[C/G]AGACCAAAAAGGGGG | 10600 |
rs772815373 | snp | C/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29050704 | TAACGTATGTAGTTC[C/T]AGAGTTTATAGTACA | 10600 |
rs772815429 | in-del | -/A | 1.64848e-05 | 0.00287091 | frameshift-variant | USP16 | GRCh38.p7 | 21:29054133 | GCAAGCTGTGCCTAC[-/A]ACTAAAGTACTAAAC | 10600 |
rs772906885 | snp | C/T | 1.91046e-05 | 0.00309062 | intron-variant | USP16 | GRCh38.p7 | 21:29043649 | TTTTATATTTTGAGC[C/T]ATTGAGTTTGTAGTC | 10600 |
rs772924322 | snp | G/T | 3.59997e-05 | 0.00424247 | intron-variant | USP16 | GRCh38.p7 | 21:29050226 | TTTAAAGTCAAATTG[G/T]GGCTTACCTAATGCT | 10600 |
rs772981965 | in-del | -/AA | 1.66065e-05 | 0.00288149 | frameshift-variant, utr-variant-5-prime | USP16 | GRCh38.p7 | 21:29037342 | AGAGTAAGAATGAAC[-/AA]GAGAGAGAAAAGAAG | 10600 |
rs773109092 | snp | C/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29041346 | TCAGAAAAGTGTGGT[C/T]CTGCATAAATTATCA | 10600 |
rs773119965 | snp | A/G | 3.32198e-05 | 0.00407539 | missense | USP16 | GRCh38.p7 | 21:29046748 | CATCCTGAAGACAGT[A/G]AATATGAAGCTGAAA | 10600 |
rs773160906 | snp | C/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29033081 | GTAACCTTTTAAATA[C/G]ATATGGTGAGTATGA | 10600 |
rs773166134 | snp | C/G | 0.00018648 | 0.00965429 | utr-variant-5-prime, upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29024678 | GGGTCACTCTGGCTT[C/G]GACTCCGTCGCTCTC | 10600 |
rs773191225 | snp | A/G | 1.69218e-05 | 0.00290871 | missense | USP16 | GRCh38.p7 | 21:29042084 | CTAACTAGTATGATC[A/G]TGTGTGATCAATGCA | 10600 |
rs773191292 | snp | A/G | 1.70837e-05 | 0.00292259 | synonymous-codon | USP16 | GRCh38.p7 | 21:29047305 | ACAGTGTAATGGACC[A/G]AAGGCAAATATAAAA | 10600 |
rs773231465 | snp | C/T | 1.64787e-05 | 0.00287038 | intron-variant | USP16 | GRCh38.p7 | 21:29054045 | TCCATTTATGTTTGA[C/T]TTTTCATTTTCTCAT | 10600 |
rs773240682 | snp | A/G | 1.84872e-05 | 0.00304027 | splice-acceptor-variant, missense, utr-variant-5-prime | USP16 | GRCh38.p7 | 21:29037278 | TCTTTTTTTAAAGCA[A/G]AGAAAGATAATGGAA | 10600 |
rs773244511 | snp | A/C | | | intron-variant | USP16 | GRCh38.p7 | 21:29053700 | TTTCTGCACTCTCAA[A/C]GTAATGGTTAAAGAC | 10600 |
rs773316118 | snp | C/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29028233 | TTCAAACGGTTCTCT[C/T]GTGCCTCAGCCTCTG | 10600 |
rs773401724 | snp | A/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29049677 | CGATCCTCCCACCTT[A/G]GCCTCTATAGTAGCT | 10600 |
rs773496827 | snp | C/G | 2.02456e-05 | 0.00318157 | intron-variant | USP16 | GRCh38.p7 | 21:29040602 | ATATCCATTTTATTA[C/G]TTTTAGAGAGTGAGT | 10600 |
rs773503467 | snp | C/T | 1.65078e-05 | 0.00287291 | synonymous-codon, utr-variant-5-prime | USP16 | GRCh38.p7 | 21:29036358 | AAAACAAGCCAGCAT[C/T]ACAACTCCAAAGCCA | 10600 |
rs773517455 | snp | G/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29052603 | TCAAGATGAGATTTG[G/T]GTAGGGACACAGCCA | 10600 |
rs773651513 | in-del | -/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29042584 | CCTGTAAGATTTTGT[-/G]GGGGGGAAGCCTTGT | 10600 |
rs773809458 | snp | C/G | 0.000205023 | 0.0101227 | utr-variant-5-prime, upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29024774 | ATGGGCTCTGTCGCC[C/G]TGGGTGAGTTCTGGT | 10600 |
rs773866009 | snp | A/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29047427 | TGGATGGCATGAATA[A/T]GTGTCCTTTTCTGTG | 10600 |
rs773882670 | in-del | -/CGTG | | | intron-variant | USP16 | GRCh38.p7 | 21:29048048 | AGCTCAGAGACGATA[-/CGTG]TGTGTGTGTGTGTGT | 10600 |
rs773899212 | snp | C/G | 1.64958e-05 | 0.00287187 | missense, utr-variant-5-prime | USP16 | GRCh38.p7 | 21:29039113 | CAAGAGACCAAAAAG[C/G]GGGTTGTGACACCGA | 10600 |
rs773900023 | in-del | -/AG | 1.64779e-05 | 0.00287031 | splice-acceptor-variant | USP16 | GRCh38.p7 | 21:29054064 | TCATTTTCTCATGAC[-/AG]ATTTTGAAATGGAAT | 10600 |
rs773909956 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29026020 | GGGAAGTTCAGTGGA[A/G]AGGTTTATTTAGAGT | 10600 |
rs773915913 | in-del | -/T | 1.65151e-05 | 0.00287355 | frameshift-variant | USP16 | GRCh38.p7 | 21:29046817 | TTTCACAAGAGGGTG[-/T]TTATGCATAAAGAAT | 10600 |
rs773934056 | snp | A/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29049234 | GATAAAAAGACATTG[A/G]TGCCTTGGATTGTCA | 10600 |
rs773973301 | snp | C/G/T | 3.34137e-05 | 0.00408729 | missense, upstream-variant-2KB, utr-variant-5-prime | USP16 | GRCh38.p7 | 21:29027947 | AAGGGAAAAACTGTT[C/G/T]CAATCGATGATTCCT | 10600 |
rs773989663 | snp | C/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29047625 | TTTTTTCCACCCTTA[C/T]CTCCTTTGCACCCAG | 10600 |
rs774158871 | snp | A/G | 1.73075e-05 | 0.00294167 | missense | USP16 | GRCh38.p7 | 21:29047315 | GGACCAAAGGCAAAT[A/G]TAAAAGGTATTTTAA | 10600 |
rs774171394 | snp | C/T | | | upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29024488 | ACTTCGTGGTTATGT[C/T]AGAGACGAGAAAACC | 10600 |
rs774176061 | snp | A/G | 1.68388e-05 | 0.00290158 | missense | USP16 | GRCh38.p7 | 21:29046713 | AAGTTCTTCATTTAA[A/G]TGATATTTGTACTAT | 10600 |
rs774208058 | in-del | -/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29032828 | TAATGTTTAGTTTTT[-/T]AAGAAACTGCCAAAC | 10600 |
rs774384199 | snp | C/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29029661 | CCAACAGAGTTTTCA[C/G]CCTCAGGTTCAACTG | 10600 |
rs774395354 | snp | C/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29039289 | ATACAAAAGGCATAG[C/T]TTTTTTTCATTTGGA | 10600 |
rs774510382 | snp | A/C | | | intron-variant | USP16 | GRCh38.p7 | 21:29031638 | AGACAGGGTTTTGCC[A/C]TGTTGGCCAGGCTGG | 10600 |
rs774549500 | snp | A/C | 1.65004e-05 | 0.00287227 | missense | USP16 | GRCh38.p7 | 21:29054152 | AAAGTACTAAACTCA[A/C]AAGCGTACCTCCTAT | 10600 |
rs774570091 | in-del | -/TAATAT | 2.17313e-05 | 0.00329624 | intron-variant | USP16 | GRCh38.p7 | 21:29039209 | TGAGATGCTGAGAAA[-/TAATAT]TAATATTAAATAGTA | 10600 |
rs774571624 | snp | C/T | 1.64776e-05 | 0.00287028 | missense | USP16 | GRCh38.p7 | 21:29054069 | TTCTCATGACAGATT[C/T]TGAAATGGAATCAAA | 10600 |
rs774638307 | snp | C/T | 1.64735e-05 | 0.00286993 | synonymous-codon, utr-variant-5-prime | USP16 | GRCh38.p7 | 21:29034882 | GCCTTGAAGCACTAT[C/T]TGACGCCAAGATCTG | 10600 |
rs774770733 | snp | G/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29036919 | AATTCATTAAAAAAT[G/T]TATTTCATGTCCATG | 10600 |
rs774856402 | snp | C/T | 1.70046e-05 | 0.00291582 | intron-variant | USP16 | GRCh38.p7 | 21:29030783 | CATCAGGTATGCTTA[C/T]GTTTTAAGATCAATA | 10600 |
rs774912728 | in-del | -/GTGT | | | intron-variant | USP16 | GRCh38.p7 | 21:29048049 | GCTCAGAGACGATAC[-/GTGT]GTGTGTGTGTGTGTG | 10600 |
rs774985078 | snp | C/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29044677 | GTCTCTAACTCCTGA[C/T]CTCAGATAATCTGCC | 10600 |
rs775007916 | in-del | -/AA | | | intron-variant | USP16 | GRCh38.p7 | 21:29049222 | TTACGGACCCTTGAT[-/AA]AAAGACATTGGTGCC | 10600 |
rs775027572 | snp | A/G | 1.65195e-05 | 0.00287393 | missense | USP16 | GRCh38.p7 | 21:29048790 | GTTTACACCAATGCC[A/G]AAAAGCAGATGCTAA | 10600 |
rs775078645 | snp | G/T | | | upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29024365 | GAAACAAATTTAAGC[G/T]TTCCCCCTTTTAGCT | 10600 |
rs775112043 | snp | G/T | 4.95716e-05 | 0.00497829 | intron-variant | USP16 | GRCh38.p7 | 21:29042468 | TCTTTTCTGATTGGT[G/T]AAGGTCTCCTTGGTT | 10600 |
rs775138607 | snp | G/T | 1.94797e-05 | 0.00312081 | intron-variant | USP16 | GRCh38.p7 | 21:29030553 | ACTGAAGAAAGTCAT[G/T]TTTGACCTTATATAT | 10600 |
rs775228880 | snp | G/T | 1.94365e-05 | 0.00311735 | intron-variant | USP16 | GRCh38.p7 | 21:29037512 | GTCCTTTTCCTCATA[G/T]AATCTGCTACTTACA | 10600 |
rs775249349 | snp | C/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29052365 | CATGGCTGGGGAGGC[C/T]TCACAGTCATGGCGG | 10600 |
rs775282066 | in-del | -/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29028290 | ACCACAGCCAGCTAA[-/T]TTTTTTTTTTTTTTT | 10600 |
rs775301329 | snp | A/G | 1.67052e-05 | 0.00289004 | intron-variant | USP16 | GRCh38.p7 | 21:29039575 | GAACACCAAGTTAGC[A/G]TGTTATGACCATTGT | 10600 |
rs775306563 | snp | A/G | 4.96019e-05 | 0.00497981 | synonymous-codon | USP16 | GRCh38.p7 | 21:29054166 | ACAAGCGTACCTCCT[A/G]TTTTATGAGAGAATA | 10600 |
rs775400608 | snp | A/G | 1.64909e-05 | 0.00287144 | missense, utr-variant-5-prime | USP16 | GRCh38.p7 | 21:29038377 | GAACTACTAAAAGAA[A/G]TGAAAATGTCTGGAA | 10600 |
rs775528180 | in-del | -/TCTT | 4.01187e-05 | 0.00447859 | intron-variant | USP16 | GRCh38.p7 | 21:29046622 | CTCCTTTTCTCCCGC[-/TCTT]TCTTTTTCTTTATTT | 10600 |
rs775557900 | snp | C/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29053429 | TAAAATACTGTTCTC[C/T]TCCTGTTCAGGGCTT | 10600 |
rs775584096 | snp | C/G | 2.02579e-05 | 0.00318254 | intron-variant | USP16 | GRCh38.p7 | 21:29040734 | TAGTTGAATTCCTCT[C/G]TACCTTAGGACAAGA | 10600 |
rs775618153 | in-del | -/ACAGTGGT | 4.94311e-05 | 0.00497123 | frameshift-variant | USP16 | GRCh38.p7 | 21:29053857 | ATGGAGTTGTTGAAC[-/ACAGTGGT]ACTATGAGGTCGGGG | 10600 |
rs775688108 | snp | C/G | 6.83585e-05 | 0.0058459 | missense | USP16 | GRCh38.p7 | 21:29040640 | TACTTAAAGCATTTG[C/G]TAATTCTACTGAAAA | 10600 |
rs775691252 | snp | C/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29034606 | ACAGGTGTGAGCCAC[C/T]GCGCCTAGCGAGTGC | 10600 |
rs775739524 | in-del | -/TTT | 1.69398e-05 | 0.00291026 | intron-variant | USP16 | GRCh38.p7 | 21:29036222 | TTATTTGTCTCCCCC[-/TTT]TTAGTTGTCATTTTG | 10600 |
rs775784738 | snp | C/T | 3.31022e-05 | 0.00406817 | synonymous-codon | USP16 | GRCh38.p7 | 21:29046972 | AACATCTTCTCCCAC[C/T]AGGAATTTAAATGGT | 10600 |
rs775839252 | snp | C/G | | | intron-variant, upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29027626 | AGGTTCTCTCCTGAC[C/G]TTTACATATATTGAA | 10600 |
rs775921523 | snp | A/G | 1.6477e-05 | 0.00287024 | missense, utr-variant-5-prime | USP16 | GRCh38.p7 | 21:29036311 | CAGTATTGTAGTTCA[A/G]ACCAGTTGGGTCAAG | 10600 |
rs776011152 | snp | A/C/G | 3.29501e-05 | 0.00405884 | missense, utr-variant-5-prime | USP16 | GRCh38.p7 | 21:29034928 | TTCTTAGTTTGGACA[A/C/G]CTGGAGTGTATGGTG | 10600 |
rs776087041 | snp | C/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29036068 | ATCATACTACTTATA[C/T]GCAGCCATAATTCTG | 10600 |
rs776135469 | snp | A/G | 3.42231e-05 | 0.00413647 | intron-variant | USP16 | GRCh38.p7 | 21:29053762 | GACATCTGTGTAAAT[A/G]GAACTAGAACTAACT | 10600 |
rs776153683 | snp | A/G | 0.000132624 | 0.00814213 | missense | USP16 | GRCh38.p7 | 21:29050108 | CTGGTTTTAACCTAC[A/G]CAAAGTTAACAAACA | 10600 |
rs776163661 | snp | A/C | 1.65168e-05 | 0.00287369 | missense | USP16 | GRCh38.p7 | 21:29048796 | ACCAATGCCAAAAAG[A/C]AGATGCTAATTTCTC | 10600 |
rs776170501 | snp | C/T | 3.32795e-05 | 0.00407905 | synonymous-codon | USP16 | GRCh38.p7 | 21:29043506 | GGAAGAAAAAGATAA[C/T]GACAGTTACATAAAA | 10600 |
rs776225503 | snp | C/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29028669 | TTGAACTCCTGACCT[C/G]AAGTGATCCGCTTCC | 10600 |
rs776267733 | snp | G/T | | | upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29022636 | CTGACAGGAAGCACG[G/T]GGTACAATGACCCTA | 10600 |
rs776284650 | snp | A/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29044214 | GCTGGGATTACAGGC[A/G]TGAGCCACCGCGCCC | 10600 |
rs776337638 | snp | A/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29029078 | TCATCGGCACTGGTT[A/G]GTATCATCTGTAAAC | 10600 |
rs776346260 | snp | G/T | 1.6912e-05 | 0.00290787 | intron-variant | USP16 | GRCh38.p7 | 21:29050075 | AAAGAAGTCAATCTG[G/T]TATGCTTCTCTTTTA | 10600 |
rs776441882 | snp | C/T | 1.65154e-05 | 0.00287358 | missense | USP16 | GRCh38.p7 | 21:29047063 | AATTTGAATGCTGCT[C/T]TTCATCCTGATGAAA | 10600 |
rs776454055 | snp | A/T | 1.67119e-05 | 0.00289062 | missense, utr-variant-5-prime | USP16 | GRCh38.p7 | 21:29030762 | TGGCTGTGTCTTAAA[A/T]GTGGCCATCAGGTAT | 10600 |
rs776469674 | in-del | -/TA | 0.000789993 | 0.0198588 | intron-variant | USP16 | GRCh38.p7 | 21:29040580 | TTTAAAATTTAATAG[-/TA]TATATATATCCATTT | 10600 |
rs776470744 | in-del | -/AAAC | 1.68522e-05 | 0.00290272 | frameshift-variant | USP16 | GRCh38.p7 | 21:29043576 | CAGAAAAAAGCAAAG[-/AAAC]AAGCCAAAAAGCAAG | 10600 |
rs776482525 | snp | C/G | 1.65111e-05 | 0.0028732 | missense, utr-variant-5-prime | USP16 | GRCh38.p7 | 21:29039050 | GAAATAAACCTTGAG[C/G]CTCCAGGCCCTCTTA | 10600 |
rs776511744 | in-del | -/CT | | | intron-variant | USP16 | GRCh38.p7 | 21:29053314 | AATAAGCAGCGTGCA[-/CT]CTCTCGTGGGGAAAG | 10600 |
rs776520356 | snp | C/T | 1.70502e-05 | 0.00291972 | intron-variant | USP16 | GRCh38.p7 | 21:29053773 | AAATGGAACTAGAAC[C/T]AACTTTTGGATTCTA | 10600 |
rs776520792 | in-del | -/TTCT | | | intron-variant | USP16 | GRCh38.p7 | 21:29044752 | TGCCTGGCCCATTCT[-/TTCT]TTCTTTCTTTCTTTC | 10600 |
rs776545481 | snp | A/G | 0.000461042 | 0.0151759 | upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29024611 | GGGGGTGGGGTGGTG[A/G]TGGCCTAGCCACTTC | 10600 |
rs776568877 | snp | A/G | 1.64933e-05 | 0.00287165 | synonymous-codon, utr-variant-5-prime | USP16 | GRCh38.p7 | 21:29038394 | GAAAATGTCTGGAAC[A/G]ATTGTAAAAATTGAA | 10600 |
rs776708140 | snp | C/G/T | 6.72929e-05 | 0.00580022 | missense | USP16 | GRCh38.p7 | 21:29042073 | TTGGTGGTGAACTAA[C/G/T]TAGTATGATCATGTG | 10600 |
rs776720884 | snp | A/G | 3.3216e-05 | 0.00407515 | utr-variant-3-prime | USP16 | GRCh38.p7 | 21:29054189 | AGAGAATACTGTAAT[A/G]ATATCAAAAGCACTT | 10600 |
rs776738445 | snp | A/G | 1.648e-05 | 0.0028705 | missense, utr-variant-5-prime | USP16 | GRCh38.p7 | 21:29036345 | TTGATTATGTCAGAA[A/G]ACAAGCCAGCATTAC | 10600 |
rs776940864 | snp | C/T | | | upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29024309 | GTAAATTCAAGACAA[C/T]TTAGGTACTCAGTTT | 10600 |
rs777103911 | snp | C/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29047582 | CTTGGAATGCAGTCA[C/G]CACAGCATCCTGACA | 10600 |
rs777128671 | in-del | -/A | 1.76902e-05 | 0.00297402 | intron-variant | USP16 | GRCh38.p7 | 21:29030825 | AAACTCTTTGAACTT[-/A]ACTTTAGAAGGTATT | 10600 |
rs777133992 | snp | A/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29045777 | TTTTGATGGTTGGTG[A/G]TGGTTTATTCCTGAT | 10600 |
rs777187829 | snp | A/T | 1.65081e-05 | 0.00287293 | missense | USP16 | GRCh38.p7 | 21:29046842 | AAGAATATTGTGTCA[A/T]CCAGAAAGATTTGAA | 10600 |
rs777188921 | snp | A/G | 1.75293e-05 | 0.00296046 | synonymous-codon | USP16 | GRCh38.p7 | 21:29046678 | CCAGAACCAACGAAG[A/G]CAACAAAAAATTCAA | 10600 |
rs777189421 | snp | C/G | 3.33817e-05 | 0.00408531 | intron-variant | USP16 | GRCh38.p7 | 21:29039477 | TCTTTTTGTTTTTCT[C/G]TAGAGCAGTGCGGTT | 10600 |
rs777198114 | snp | A/G | 1.64746e-05 | 0.00287002 | missense | USP16 | GRCh38.p7 | 21:29053910 | GCCAAGGCAAGAACC[A/G]CAAATAGTCATCTCT | 10600 |
rs777226840 | in-del | -/TGATCTTT | | | intron-variant | USP16 | GRCh38.p7 | 21:29031258 | ATCTTTGGCAGTGAG[-/TGATCTTT]GGCATGTCTGGCTGG | 10600 |
rs777244389 | snp | A/G | 3.29457e-05 | 0.00405854 | intron-variant | USP16 | GRCh38.p7 | 21:29036412 | TATACACCAAATGTC[A/G]ATTTGTGTATCTGCT | 10600 |
rs777258940 | snp | A/G | | | missense, utr-variant-5-prime | USP16 | GRCh38.p7 | 21:29038335 | CACCCTACATTCTAG[A/G]ACTTGTCACAAACAC | 10600 |
rs777408626 | snp | C/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29028883 | AGTAGTAAACAACTT[C/T]ATAGCTAAATCTCTC | 10600 |
rs777413791 | snp | C/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29051915 | AAGATTATGGTCACA[C/T]TGAGGACTATGACAA | 10600 |
rs777461538 | snp | A/C | | | intron-variant | USP16 | GRCh38.p7 | 21:29030455 | TATTCAAATATCAAA[A/C]AATTTTAAGTTCAGA | 10600 |
rs777465468 | snp | A/G | 3.29636e-05 | 0.00405964 | intron-variant | USP16 | GRCh38.p7 | 21:29053998 | CACTCAGCAGATTAC[A/G]GCAAAACCAAAAAGT | 10600 |
rs777508584 | in-del | -/C | 1.67706e-05 | 0.00289569 | intron-variant | USP16 | GRCh38.p7 | 21:29038320 | TTTCTCTTTTTTTTT[-/C]ACCCTACATTCTAGA | 10600 |
rs777525482 | snp | A/G | 1.65416e-05 | 0.00287586 | missense, utr-variant-5-prime | USP16 | GRCh38.p7 | 21:29030634 | AAGGATTGGAACAAG[A/G]TAATTTGAAAAAGGC | 10600 |
rs777613123 | snp | A/C | 1.90141e-05 | 0.00308329 | intron-variant | USP16 | GRCh38.p7 | 21:29028010 | CTTTAATGTTTATAT[A/C]TCTAAATGAATATGT | 10600 |
rs777666093 | snp | C/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29047908 | GAGACAAAAAGTAAG[C/G]CTGTGTGTGTGTGTA | 10600 |
rs777703233 | in-del | -/TTCT | | | intron-variant | USP16 | GRCh38.p7 | 21:29044749 | ACCGTGCCTGGCCCA[-/TTCT]TTCTTTCTTTCTTTC | 10600 |
rs777767396 | snp | C/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29043928 | TAAGTCCCCCTCCCA[C/T]CACTGTTTTTTTTTT | 10600 |
rs777786241 | snp | C/T | 8.2603e-05 | 0.00642609 | missense | USP16 | GRCh38.p7 | 21:29046803 | TTAAATCCAACCATA[C/T]TTCACAAGAGGGTGT | 10600 |
rs777789584 | in-del | -/CTT | 1.7307e-05 | 0.00294163 | intron-variant | USP16 | GRCh38.p7 | 21:29050048 | ACTTAACCTGTATTG[-/CTT]CTTTTCCAAGAAAAG | 10600 |
rs777967116 | snp | A/G | 1.65864e-05 | 0.00287974 | synonymous-codon, utr-variant-5-prime | USP16 | GRCh38.p7 | 21:29037439 | TAATTTGGGAAACAC[A/G]TGTTTCTTCAATGCA | 10600 |
rs778065460 | snp | A/C | 1.77307e-05 | 0.00297742 | missense | USP16 | GRCh38.p7 | 21:29043441 | GGTAAGAAAAGTGTA[A/C]ATGATAAAAATCTGA | 10600 |
rs778081837 | snp | C/T | 1.66921e-05 | 0.00288891 | intron-variant | USP16 | GRCh38.p7 | 21:29048864 | TCAGCAGGTACTCCT[C/T]GTTACCCAAAATTTG | 10600 |
rs778094776 | snp | A/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29040479 | ATTAAGTTTGAAAAT[A/G]TGATTTTGGAATTAT | 10600 |
rs778131851 | snp | A/C | 1.65446e-05 | 0.00287612 | missense | USP16 | GRCh38.p7 | 21:29046946 | AACATGGATAATGAT[A/C]TGGAGGTTTTAACAT | 10600 |
rs778147648 | snp | C/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29025484 | TCACAATATGCTCTC[C/T]TCATGACTCATTAGT | 10600 |
rs778171578 | snp | A/G | 1.65652e-05 | 0.0028779 | missense | USP16 | GRCh38.p7 | 21:29048767 | TTTCTTTAGGTGAAA[A/G]GAAGCATGTTTACAC | 10600 |
rs778242626 | snp | A/G | 4.96438e-05 | 0.00498191 | missense | USP16 | GRCh38.p7 | 21:29047010 | TAACGGAAGGGAGCA[A/G]TGGAGAAGTGGACAT | 10600 |
rs778258110 | snp | A/G | 1.64874e-05 | 0.00287113 | missense | USP16 | GRCh38.p7 | 21:29054140 | GTGCCTACAACTAAA[A/G]TACTAAACTCACAAG | 10600 |
rs778275945 | in-del | -/TT | 0.000108266 | 0.00735672 | intron-variant, upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29027834 | AAATATAAGACATAC[-/TT]TTTTTTTTGGTCAAG | 10600 |
rs778336319 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29027045 | CTGAACTCCCACATC[A/G]ATTAGAGTGAGTTGG | 10600 |
rs778348509 | snp | C/T | 1.65176e-05 | 0.00287376 | synonymous-codon, utr-variant-5-prime | USP16 | GRCh38.p7 | 21:29039539 | CTGCTTCGCTACTTA[C/T]TGGATGGGATGAGAG | 10600 |
rs778564021 | snp | A/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29042735 | AAAGATGATGTATTC[A/G]GAATTCTGTACAAGT | 10600 |
rs778610116 | snp | A/G | 1.70472e-05 | 0.00291947 | intron-variant | USP16 | GRCh38.p7 | 21:29048892 | TTGTTTTAAATATGT[A/G]ACACCTACTTTATTA | 10600 |
rs778629546 | snp | C/T | 1.65353e-05 | 0.00287531 | missense | USP16 | GRCh38.p7 | 21:29046920 | CAGAGGAAGTAGATA[C/T]GAAAAATATCAACAT | 10600 |
rs778636997 | snp | C/T | 1.65021e-05 | 0.00287241 | intron-variant | USP16 | GRCh38.p7 | 21:29034815 | TTTATGGCTTTGAGG[C/T]TTATGATTATGATTT | 10600 |
rs778648132 | snp | A/G | 1.65173e-05 | 0.00287374 | synonymous-codon | USP16 | GRCh38.p7 | 21:29046813 | CCATATTTCACAAGA[A/G]GGTGTTATGCATAAA | 10600 |
rs778663102 | snp | C/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29033856 | AGATAAGTATAGGCT[C/T]CTGGGAGGAGGTGGC | 10600 |
rs778712840 | snp | G/T | | | | | GRCh38.p7 | 21:29041329 | CCTGCTGGCATTTTC[G/T]GTCAGAAAAGTGTGG | 10600 |
rs778714297 | snp | A/G | | | | | GRCh38.p7 | 21:29044509 | TGGAGTGCAAATGGC[A/G]AGATCTTGGCACACT | 10600 |
rs778720088 | snp | C/T | | | | | GRCh38.p7 | 21:29035084 | CACAAAGCTAAAGAA[C/T]GCAGTATTATGAGAA | 10600 |
rs778720183 | in-del | -/TT | | | | | GRCh38.p7 | 21:29046396 | TTGTGATCATCTTGC[-/TT]TTTGGCCTTCCACAG | 10600 |
rs778725826 | in-del | -/GGT | 0.000480192 | 0.0154876 | | | GRCh38.p7 | 21:29024603 | GGGAGGTGGGGGTGG[-/GGT]GGTGGTGGTGGCCTA | 10600 |
rs778735959 | snp | C/T | 3.29592e-05 | 0.00405938 | | | GRCh38.p7 | 21:29054020 | CCAAAAAGTAATCAA[C/T]TTGAATCTTTCCATT | 10600 |
rs778864259 | snp | A/G | 1.64836e-05 | 0.0028708 | missense, utr-variant-5-prime | USP16 | GRCh38.p7 | 21:29030679 | AATGGAATATCTGCC[A/G]AGACTGTAAGACTGA | 10600 |
rs778895060 | snp | A/G | 1.65236e-05 | 0.00287429 | missense | USP16 | GRCh38.p7 | 21:29048785 | AGCATGTTTACACCA[A/G]TGCCAAAAAGCAGAT | 10600 |
rs778990777 | snp | A/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29025376 | TTTGTATGGAGTCCT[A/G]CGAAGAGTCATTTCA | 10600 |
rs779004698 | snp | G/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29048271 | TATTTTTAATAGAGA[G/T]AGGGTTTCGCCACGT | 10600 |
rs779023189 | snp | A/G | 1.68088e-05 | 0.00289899 | missense | USP16 | GRCh38.p7 | 21:29043471 | AAAAAGACAGTGGAG[A/G]ATGAAGATCAAGATA | 10600 |
rs779042233 | in-del | -/TTC | 1.68775e-05 | 0.0029049 | intron-variant | USP16 | GRCh38.p7 | 21:29048745 | CTCCCTGTTAAAAAT[-/TTC]TTCTTTTCTTTAGGT | 10600 |
rs779049518 | in-del | -/A | 3.68189e-05 | 0.00429046 | frameshift-variant | USP16 | GRCh38.p7 | 21:29043432 | TTTAAGAGTGGTAAG[-/A]AAAGTGTAAATGATA | 10600 |
rs779055745 | snp | A/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29036136 | TAGTCTTCTTCAGGA[A/G]AACAGAATTTTTACG | 10600 |
rs779121508 | snp | G/T | 1.73393e-05 | 0.00294437 | intron-variant | USP16 | GRCh38.p7 | 21:29043603 | AAGCAAGCCAAGGTG[G/T]GTAATTAGGAGGAAA | 10600 |
rs779204233 | snp | A/C | 1.68448e-05 | 0.00290209 | intron-variant | USP16 | GRCh38.p7 | 21:29039010 | TGAAGAAAGTAATTT[A/C]TTTTCCCATATTCAG | 10600 |
rs779223610 | snp | C/G | 1.72463e-05 | 0.00293647 | missense | USP16 | GRCh38.p7 | 21:29042103 | GTGATCAATGCAGAA[C/G]TGTAAGTAGATGTCA | 10600 |
rs779241595 | snp | A/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29053101 | GAGAATCATAGATGG[A/G]CGGAGAAGTACTAAG | 10600 |
rs779269032 | in-del | -/TT | | | intron-variant | USP16 | GRCh38.p7 | 21:29037589 | GAAAACTTTTTTTTT[-/TT]TTTTTTTTTTTTTTG | 10600 |
rs779277404 | snp | A/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29034134 | TGTATGAACAGAGCT[A/T]TGTTTTAGGAACACT | 10600 |
rs779308743 | snp | A/G | 8.24722e-05 | 0.006421 | missense, utr-variant-5-prime | USP16 | GRCh38.p7 | 21:29036278 | GGTCACAGGTGTTAC[A/G]TATGTGATAATGAGG | 10600 |
rs779317832 | snp | A/C | | | upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29023691 | TTGCAACCTCTGCCT[A/C]CAGACTTCAAGCGAT | 10600 |
rs779333792 | snp | A/G | 1.64868e-05 | 0.00287109 | synonymous-codon | USP16 | GRCh38.p7 | 21:29047125 | TCCTGGAACAAAGGT[A/G]TATGAGGTTGTAAAT | 10600 |
rs779373110 | snp | A/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29051597 | ACACTTTGGGAGGCC[A/G]AGGCGGGTGGATCAC | 10600 |
rs779427386 | snp | C/G | 3.30803e-05 | 0.00406682 | missense | USP16 | GRCh38.p7 | 21:29047023 | CAATGGAGAAGTGGA[C/G]ATTTCCAATGGTTTC | 10600 |
rs779439348 | in-del | -/CT | | | downstream-variant-500B | USP16 | GRCh38.p7 | 21:29054723 | GTTCACGCCATTCTC[-/CT]GTCTCAGCCTCCCGA | 10600 |
rs779484099 | snp | A/G | 1.64844e-05 | 0.00287087 | missense, utr-variant-5-prime | USP16 | GRCh38.p7 | 21:29030705 | ACTGACAATAAAGTG[A/G]AAGATAAAGCTGAAG | 10600 |
rs779509003 | in-del | -/TGTGTGTGTGTT | | | intron-variant | USP16 | GRCh38.p7 | 21:29048088 | GTGTGTGTGTGTGTG[-/TGTGTGTGTGTT]TTGAGACAGAGTCCT | 10600 |
rs779518728 | snp | A/G | 8.27561e-05 | 0.00643205 | synonymous-codon | USP16 | GRCh38.p7 | 21:29046999 | TGGTGCCTACCTAAC[A/G]GAAGGGAGCAATGGA | 10600 |
rs779544611 | in-del | -/TTTTTTTT | | | downstream-variant-500B | USP16 | GRCh38.p7 | 21:29054602 | TACAAGTGTGTTAAT[-/TTTTTTTT]TTTTTTTTTTTTTTT | 10600 |
rs779679589 | snp | C/T | 3.295e-05 | 0.00405881 | missense, utr-variant-5-prime | USP16 | GRCh38.p7 | 21:29034853 | GCTGTGGCAGAAATT[C/T]TCAGGAGCAGCATGC | 10600 |
rs779700165 | in-del | -/AA | | | intron-variant, upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29026456 | GCAAGACTCCGTCTC[-/AA]AAAAAAAAAAAAAAA | 10600 |
rs779765823 | snp | A/T | 1.80335e-05 | 0.00300273 | missense | USP16 | GRCh38.p7 | 21:29040686 | AAAAAATAAAGTTAA[A/T]GGTAATGTCTGACTT | 10600 |
rs779783851 | snp | C/T | 6.89441e-05 | 0.00587089 | intron-variant | USP16 | GRCh38.p7 | 21:29040577 | AAATTTAAAATTTAA[C/T]AGTATATATATATCC | 10600 |
rs779790431 | snp | A/G | 1.65384e-05 | 0.00287557 | missense | USP16 | GRCh38.p7 | 21:29046931 | GATATGAAAAATATC[A/G]ACATGGATAATGATC | 10600 |
rs779824433 | snp | A/G | | | missense | USP16 | GRCh38.p7 | 21:29047165 | GAAACTGCTTTCTGT[A/G]CTCTTGCAAACAGGG | 10600 |
rs779950927 | snp | C/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29037036 | TACCAAAGCACATAC[C/T]GTTTGGTTTCATTTA | 10600 |
rs779957098 | snp | G/T | 1.7051e-05 | 0.0029198 | intron-variant | USP16 | GRCh38.p7 | 21:29050192 | AGGTAAGTCAAAGTG[G/T]TCTTTTTCAGGAAAG | 10600 |
rs779995844 | snp | C/G | 0.000190613 | 0.00976065 | intron-variant | USP16 | GRCh38.p7 | 21:29050041 | TTCGGTTTACTTAAC[C/G]TGTATTGCTTTTCCA | 10600 |
rs780004484 | snp | A/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29041036 | ATGTGGCGTGTAAAG[A/G]TTTAGGGCAGATCTG | 10600 |
rs780105701 | in-del | -/TGAC | 1.70326e-05 | 0.00291822 | intron-variant | USP16 | GRCh38.p7 | 21:29038991 | AGTGATTCCAGAATT[-/TGAC]TGAAGAAAGTAATTT | 10600 |
rs780220734 | snp | A/T | 3.2963e-05 | 0.00405961 | missense | USP16 | GRCh38.p7 | 21:29047160 | ATCCAGAAACTGCTT[A/T]CTGTACTCTTGCAAA | 10600 |
rs780268519 | snp | C/G/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29046052 | TGGTTTCAAACTCCT[C/G/T]ACCTCAAGTGAGATG | 10600 |
rs780278556 | in-del | -/CA | | | intron-variant | USP16 | GRCh38.p7 | 21:29041738 | AGTCTCACTGACTTG[-/CA]CAGTTTACTTCCCAC | 10600 |
rs780344631 | snp | A/G | 1.79014e-05 | 0.00299172 | splice-acceptor-variant, upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29027871 | TTTATCTTGTTTTCT[A/G]GATTGTTATTTTGTG | 10600 |
rs780430880 | snp | A/C | | | intron-variant | USP16 | GRCh38.p7 | 21:29036780 | TTTCCATGCATAATT[A/C]AATTAATTGGCTGAC | 10600 |
rs780459691 | snp | C/T | 1.65323e-05 | 0.00287505 | stop-gained | USP16 | GRCh38.p7 | 21:29047249 | CGTAATGAGAAACTT[C/T]GAGATGCGAATAAAC | 10600 |
rs780484909 | in-del | -/T | 3.34345e-05 | 0.00408853 | intron-variant | USP16 | GRCh38.p7 | 21:29042561 | TTTTATTCAAGTAGA[-/T]TTTTTTTTCCTGTAA | 10600 |
rs780485294 | snp | C/T | 1.79493e-05 | 0.00299572 | intron-variant | USP16 | GRCh38.p7 | 21:29042125 | TAGATGTCATGTATA[C/T]TGGGTTTATTTGCTA | 10600 |
rs780555829 | snp | G/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29032253 | TTTTCTTTTTTTGAG[G/T]CAGGGTCTCACTCTC | 10600 |
rs780556874 | snp | A/G | 0.000151114 | 0.00869105 | missense | USP16 | GRCh38.p7 | 21:29042052 | CAAGTTTTGTTGACC[A/G]CATCTTTGGTGGTGA | 10600 |
rs780606857 | in-del | -/TTTTTTTTTTT | | | intron-variant | USP16 | GRCh38.p7 | 21:29037580 | GTATCCAAAGAAAAC[-/TTTTTTTTTTT]TTTTTTTTTTTTTTG | 10600 |
rs780610339 | snp | C/T | 0.000148252 | 0.00860837 | synonymous-codon | USP16 | GRCh38.p7 | 21:29053891 | GGGGCATTACACTGC[C/T]TATGCCAAGGCAAGA | 10600 |
rs780659816 | snp | C/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29053276 | TCCTGTTGCCAGCCC[C/T]ATGGCATATAGAGTC | 10600 |
rs780804187 | in-del | -/A | | | intron-variant | USP16 | GRCh38.p7 | 21:29049126 | TTTCAGGTTAAAAAA[-/A]GAAAAAGACTGGTGT | 10600 |
rs780817166 | snp | A/G | 1.67086e-05 | 0.00289033 | missense, upstream-variant-2KB, utr-variant-5-prime | USP16 | GRCh38.p7 | 21:29027914 | CCATAAAGTGCCAAC[A/G]TGGGAAAGAAACGGA | 10600 |
rs780824218 | snp | A/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29038667 | TTCTTGGGAATGTGT[A/G]TATGTTTGAGAAGCC | 10600 |
rs780899688 | snp | C/G/T | 1.65682e-05 | 0.00287817 | missense | USP16 | GRCh38.p7 | 21:29054177 | TCCTATTTTATGAGA[C/G/T]AATACTGTAATAATA | 10600 |
rs780916917 | snp | A/T | 1.65696e-05 | 0.00287828 | intron-variant | USP16 | GRCh38.p7 | 21:29036256 | CATTTTTCATCTCTG[A/T]TTTTTGGGTCACAGG | 10600 |
rs780920074 | snp | A/T | 3.83076e-05 | 0.00437634 | intron-variant | USP16 | GRCh38.p7 | 21:29040715 | TTTTTGAACTAAAAC[A/T]CTATAGTTGAATTCC | 10600 |
rs780933169 | snp | C/G | 1.64741e-05 | 0.00286998 | missense, utr-variant-5-prime | USP16 | GRCh38.p7 | 21:29034861 | AGAAATTCTCAGGAG[C/G]AGCATGCCTTGAAGC | 10600 |
rs780934591 | snp | A/G | 1.6517e-05 | 0.00287372 | missense, utr-variant-5-prime | USP16 | GRCh38.p7 | 21:29039507 | TTAAAGGCTATCAGC[A/G]GCAAGACAGCCAGGA | 10600 |
rs780974322 | snp | A/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29048139 | CCCAGGCTAAAGTGC[A/G]GTGGCCAATTTCAGC | 10600 |
rs780997217 | snp | A/G/T | 0.000231468 | 0.0107556 | missense | USP16 | GRCh38.p7 | 21:29047031 | AAGTGGACATTTCCA[A/G/T]TGGTTTCAAAAACCT | 10600 |
rs781022607 | snp | C/T | 1.66513e-05 | 0.00288537 | intron-variant | USP16 | GRCh38.p7 | 21:29039183 | CTTCGATTGTGCTTT[C/T]AGTGCCTCAGTGAGA | 10600 |
rs781087633 | snp | C/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29045952 | CTGGGATTACAGGCG[C/T]GCACCACCCATGTGT | 10600 |
rs781140970 | snp | C/G/T | 0.000306704 | 0.0123799 | intron-variant | USP16 | GRCh38.p7 | 21:29043625 | AGGAGGAAAATCATA[C/G/T]GCTTGTAATTTTATA | 10600 |
rs781221163 | snp | G/T | 1.64792e-05 | 0.00287042 | missense | USP16 | GRCh38.p7 | 21:29053848 | ATTCCTTATATGGAG[G/T]TGTTGAACACAGTGG | 10600 |
rs781349677 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29027156 | GTACTTTTAGCACTT[C/T]TCATGTTTTCTAAGT | 10600 |
rs781375226 | snp | G/T | 1.87145e-05 | 0.00305891 | intron-variant | USP16 | GRCh38.p7 | 21:29042145 | TTTATTTGCTAATAT[G/T]CAACAGTTTATCAAT | 10600 |
rs781451971 | snp | A/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29028704 | CATCCCAAAGTGCTG[A/G]GATTACAGGCGTGAG | 10600 |
rs781462691 | snp | A/T | 3.34711e-05 | 0.00409078 | intron-variant | USP16 | GRCh38.p7 | 21:29048751 | GTTAAAAATTTCTTC[A/T]TTTCTTTAGGTGAAA | 10600 |
rs781474829 | snp | G/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29036706 | AGATTTCAGTCTGTC[G/T]GCTGGGATAACATAA | 10600 |
rs781492599 | snp | A/T | 3.30213e-05 | 0.00406319 | missense, utr-variant-5-prime | USP16 | GRCh38.p7 | 21:29037420 | TAACCGTGAAAGGAC[A/T]CAGTAATTTGGGAAA | 10600 |
rs781549799 | snp | C/T | 4.9436e-05 | 0.00497148 | intron-variant | USP16 | GRCh38.p7 | 21:29054030 | ATCAACTTGAATCTT[C/T]CCATTTATGTTTGAT | 10600 |
rs781574322 | snp | A/G | 1.65441e-05 | 0.00287607 | intron-variant | USP16 | GRCh38.p7 | 21:29042537 | TGATCAGGTAAGACT[A/G]TTGAATTTATTTTAT | 10600 |
rs781590124 | in-del | -/A | 1.70632e-05 | 0.00292084 | frameshift-variant | USP16 | GRCh38.p7 | 21:29042023 | ATAGATTATGAGAAG[-/A]AAAAAATCAATGCCA | 10600 |
rs781610414 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP16 | GRCh38.p7 | 21:29026934 | TAAAGGCCTATGAGT[A/G]CAAAGTTTAGGGAGT | 10600 |
rs781736806 | snp | A/G | 2.27301e-05 | 0.00337113 | intron-variant | USP16 | GRCh38.p7 | 21:29037247 | ATGACTGTATTACAC[A/G]TTTTGCTAAATCTTT | 10600 |
rs781768521 | snp | C/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29050356 | ATTTTGAAGAATGGG[C/T]TATTTCAGTTCAACG | 10600 |
rs796173178 | in-del | -/A | | | intron-variant | USP16 | GRCh38.p7 | 21:29051829 | GCAAGAAACTCCCTC[-/A]AAAAAAAAAAAAAAG | 10600 |
rs796243654 | in-del | -/TT | | | intron-variant | USP16 | GRCh38.p7 | 21:29044448 | AAAACTTCTTCATTC[-/TT]TTTTTTTTTTTTTTT | 10600 |
rs796279994 | snp | C/G | | | intron-variant | USP16 | GRCh38.p7 | 21:29031682 | ATTTCAAGTGATCCA[C/G]TCACCTTGGCTCCCT | 10600 |
rs796502641 | in-del | -/AGTA | | | intron-variant | USP16 | GRCh38.p7 | 21:29037919 | GTTTTATTGCATGAC[-/AGTA]AGAGAGTTTGGTGAG | 10600 |
rs796644648 | in-del | -/AG | | | intron-variant | USP16 | GRCh38.p7 | 21:29048265 | TTTTGTATTTTTAAT[-/AG]AGAGATAGGGTTTCG | 10600 |
rs796782997 | in-del | -/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29043933 | CCCCTCCCACCACTG[-/T]TTTTTTTTTTCCAAC | 10600 |
rs796953538 | in-del | -/T | | | intron-variant | USP16 | GRCh38.p7 | 21:29039289 | ATACAAAAGGCATAG[-/T]TTTTTTTCATTTGGA | 10600 |