SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs11255 | snp | A/G | 0.443464 | 0.15834 | utr-variant-3-prime | USP47 | GRCh38.p7 | 11:11958045 | TGTAAGAGGACAGCT[A/G]TTTGGTTCTGATACA | 55031 |
rs13903 | snp | C/T | 0.263809 | 0.249618 | utr-variant-3-prime | USP47 | GRCh38.p7 | 11:11958850 | GTGTGTGAAGCAGCC[C/T]TCACACTAGAGTGTT | 55031 |
rs996428 | snp | A/G | 0.403158 | 0.197592 | upstream-variant-2KB, intron-variant | USP47, LOC107984311 | GRCh38.p7 | 11:11840131 | TTCAAGGTGAAAACC[A/G]TTCACCTTGGGCACA | 55031 |
rs1979687 | snp | A/G | 0.460477 | 0.134905 | utr-variant-3-prime | USP47 | GRCh38.p7 | 11:11958127 | GACTGACTTGCTATC[A/G]CACAAAAGAGGCAGA | 55031 |
rs2279566 | snp | A/G | 0.242488 | 0.249887 | utr-variant-3-prime | USP47 | GRCh38.p7 | 11:11958902 | GGGAAGGTACTTTAA[A/G]ATTCTGGGAAGATGC | 55031 |
rs2307073 | snp | C/T | 0.258732 | 0.249847 | synonymous-codon | USP47 | GRCh38.p7 | 11:11956026 | GAAGAATTAATGGAA[C/T]TGACAGATGAGCAAA | 55031 |
rs3215040 | in-del | -/G | 0.163983 | 0.234736 | intron-variant | USP47 | GRCh38.p7 | 11:11955958 | ATTAATAGAGGTGGA[-/G]GGGCTCTACTGGACT | 55031 |
rs3923422 | snp | C/T | | | intron-variant | USP47 | GRCh38.p7 | 11:11898928 | agttactatgagaat[C/T]aagtgagtctatata | 55031 |
rs4243945 | snp | A/G/T | 0.390838 | 0.206555 | intron-variant | USP47 | GRCh38.p7 | 11:11901246 | ATTCCCAAAAGAAAA[A/G/T]AAAAAGTCTTTTAGT | 55031 |
rs4255536 | snp | C/T | 0.288386 | 0.247035 | intron-variant | USP47 | GRCh38.p7 | 11:11845615 | TTTGTAGGTTTTGTA[C/T]TATAGGTTTAAGACA | 55031 |
rs4259823 | snp | A/G | 0.121022 | 0.21416 | intron-variant | USP47 | GRCh38.p7 | 11:11858671 | GGAGTCATATAGTAT[A/G]GTAGCATTTTGGGTA | 55031 |
rs4281479 | snp | A/C | 0.00993419 | 0.0697739 | intron-variant | USP47 | GRCh38.p7 | 11:11911395 | AGCAAAAGGCATAAA[A/C]CTACAGATCTGAGTA | 55031 |
rs4281480 | snp | A/G | 0.247053 | 0.249983 | intron-variant | USP47 | GRCh38.p7 | 11:11919579 | TCCAGGATCCTCATT[A/G]TACATTTCCAAATGG | 55031 |
rs4288751 | snp | A/C | 0.415399 | 0.187465 | intron-variant | USP47 | GRCh38.p7 | 11:11854289 | GTTATTTGTTATTTC[A/C]GTTAATACCTTCTAT | 55031 |
rs4301783 | snp | C/T | | | intron-variant | USP47 | GRCh38.p7 | 11:11877789 | TCTCTCTCTCTCTCT[C/T]TCTCTCTCTCTCTCT | 55031 |
rs4332522 | snp | A/G | 0.289165 | 0.246913 | intron-variant | USP47 | GRCh38.p7 | 11:11874806 | TCAGGTGATCCACTC[A/G]CCTTGGCCTCCCAAA | 55031 |
rs4360694 | snp | C/T | 0.293037 | 0.246268 | intron-variant | USP47 | GRCh38.p7 | 11:11897151 | ACAGGGGTAACTGGT[C/T]CTGTATAGTCTTTCT | 55031 |
rs4405306 | snp | C/T | 0.288906 | 0.246954 | intron-variant | USP47 | GRCh38.p7 | 11:11874790 | TCTTGAACTCCTGAC[C/T]TCAGGTGATCCACTC | 55031 |
rs4444076 | snp | A/G | 0.289942 | 0.246789 | intron-variant | USP47 | GRCh38.p7 | 11:11919639 | GCACAGTGTTTTTCA[A/G]TCTTTATAACTAGTG | 55031 |
rs4457743 | snp | C/T | 0.29278 | 0.246313 | intron-variant | USP47 | GRCh38.p7 | 11:11854485 | ATGTAATGTGTCATG[C/T]ACACAATAAGCTATC | 55031 |
rs4501979 | snp | C/G | | | intron-variant | USP47 | GRCh38.p7 | 11:11877807 | TCTCTCTCTCTCTCT[C/G]TGTGTGTGTGTGTGT | 55031 |
rs4597067 | snp | A/G | 0.288906 | 0.246954 | intron-variant | USP47 | GRCh38.p7 | 11:11883737 | CTCTCTCATCCACCA[A/G]CTAGAGTATATTAGA | 55031 |
rs4622254 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | USP47 | GRCh38.p7 | 11:11888479 | aattcctggacacat[A/G]caccgttccaagact | 55031 |
rs4625461 | snp | A/G | 0.289942 | 0.246789 | intron-variant | USP47 | GRCh38.p7 | 11:11891132 | CCACATCCTGCGCAG[A/G]TACACCTGAACTTAA | 55031 |
rs4757270 | snp | G/T | 0.0111196 | 0.0737302 | intron-variant | USP47 | GRCh38.p7 | 11:11925399 | TGAGCCACCGCACCC[G/T]GCCTCCTTAATGTTT | 55031 |
rs4910030 | snp | C/T | 0.290201 | 0.246747 | intron-variant | USP47 | GRCh38.p7 | 11:11856783 | TTAACCTTTCTAGTA[C/T]ACAACATATTCTTGT | 55031 |
rs4910031 | snp | C/T | 0.478354 | 0.101757 | intron-variant | USP47 | GRCh38.p7 | 11:11900778 | AGATGACTAAAGTAA[C/T]GGCAAGTACCAGCAA | 55031 |
rs4910427 | snp | C/T | 0.289165 | 0.246913 | intron-variant | USP47 | GRCh38.p7 | 11:11853901 | GGAGGCCGAGATGGG[C/T]GGATCACGAGGTCAG | 55031 |
rs4910428 | snp | C/T | 0.286825 | 0.247273 | intron-variant, utr-variant-5-prime | USP47 | GRCh38.p7 | 11:11909592 | GTGTATTTTGTCATA[C/T]AACATTTATTTAGGG | 55031 |
rs4910429 | snp | C/T | 0.391397 | 0.206172 | intron-variant, utr-variant-5-prime | USP47 | GRCh38.p7 | 11:11909751 | CTGCATAATTTCATA[C/T]AGTGCCTTTGGAGAA | 55031 |
rs6416114 | snp | C/G | 0.0912534 | 0.193131 | intron-variant | USP47 | GRCh38.p7 | 11:11911505 | caaagaaaattacca[C/G]agacagagagggctg | 55031 |
rs6485258 | snp | C/G | 0.301177 | 0.244706 | intron-variant, upstream-variant-2KB | USP47, LOC107984311 | GRCh38.p7 | 11:11843153 | GAAATTAACTGTGTG[C/G]GATCTTGAAATTAAT | 55031 |
rs6485262 | snp | A/C | 0.0310518 | 0.120672 | intron-variant | USP47 | GRCh38.p7 | 11:11850100 | tatgtagttatatgt[A/C]tgtttttttaattca | 55031 |
rs6485303 | snp | C/T | 0.267908 | 0.249358 | intron-variant | USP47 | GRCh38.p7 | 11:11933671 | TGGTGTGAGACATAA[C/T]TGGTGTCAATTACTA | 55031 |
rs7101853 | snp | C/T | 0.157311 | 0.232183 | intron-variant | USP47 | GRCh38.p7 | 11:11882969 | ATTTCTGTATTTTTA[C/T]TTGCCTCCTGTACAT | 55031 |
rs7106135 | snp | A/G | 0.29046 | 0.246704 | intron-variant | USP47 | GRCh38.p7 | 11:11893748 | AGATGAGGTCTCACT[A/G]TGTTGCCCAGGCTAG | 55031 |
rs7108356 | snp | A/C | 0.147321 | 0.227941 | intron-variant | USP47 | GRCh38.p7 | 11:11881455 | TTAGCTGTTTCCTGG[A/C]CTCTATGTCTTGACC | 55031 |
rs7109869 | snp | C/T | 0.0310518 | 0.120672 | intron-variant | USP47 | GRCh38.p7 | 11:11899466 | CTCATTTAGAGCTTC[C/T]TTAGGTAAACCTATA | 55031 |
rs7111921 | snp | C/T | 0.458545 | 0.137872 | intron-variant | USP47 | GRCh38.p7 | 11:11895100 | TAATTATTAATATTG[C/T]TGATATTATTATGAA | 55031 |
rs7111984 | snp | A/G | 0.459914 | 0.13578 | intron-variant | USP47 | GRCh38.p7 | 11:11854964 | GCCGGGTGCAGTGGC[A/G]GGCGCCTGTAGTCCC | 55031 |
rs7113259 | snp | A/G | 0.0437281 | 0.141251 | intron-variant | USP47 | GRCh38.p7 | 11:11930641 | TTCATGCTTAGAAGT[A/G]GAATCTTTTTAATCT | 55031 |
rs7122656 | snp | C/T | 0.137867 | 0.223442 | intron-variant | USP47 | GRCh38.p7 | 11:11878348 | ATTTTATACCAGGAA[C/T]GCTGAATCATTCAGA | 55031 |
rs7124866 | snp | A/T | 0.0433465 | 0.140692 | intron-variant | USP47 | GRCh38.p7 | 11:11906014 | CCTACTTTAAATATT[A/T]AGTTTAAAAAATATA | 55031 |
rs7124983 | snp | C/T | 0.0799831 | 0.183287 | intron-variant | USP47 | GRCh38.p7 | 11:11906092 | TAATTATTCATATAC[C/T]GAGTATCTGATTGGA | 55031 |
rs7126144 | snp | C/T | 0.301681 | 0.2446 | intron-variant | USP47 | GRCh38.p7 | 11:11893772 | AGGCTAGTCTCAAAG[C/T]GATCTTCCTGACTCA | 55031 |
rs7128291 | snp | G/T | 0.460252 | 0.135255 | intron-variant | USP47 | GRCh38.p7 | 11:11864294 | TGTTGGAAACCTAGT[G/T]TGTTGGCAGTTTTGC | 55031 |
rs7129520 | snp | C/T | 0.0441095 | 0.141807 | intron-variant | USP47 | GRCh38.p7 | 11:11930245 | gagccaaatccaacc[C/T]gcctccatattttgg | 55031 |
rs7395255 | snp | C/G | 0.406641 | 0.194842 | intron-variant | USP47 | GRCh38.p7 | 11:11925045 | tccagttcatgaaca[C/G]aggatgtctttccat | 55031 |
rs7480094 | snp | G/T | | | intron-variant | USP47 | GRCh38.p7 | 11:11950275 | TGTATTTGAACATAG[G/T]TCATTTTTCTTTGGT | 55031 |
rs7480817 | snp | A/T | 0.337614 | 0.234145 | intron-variant | USP47 | GRCh38.p7 | 11:11920930 | GGGCTTAATTTCTTG[A/T]ACTTACCTACTATTT | 55031 |
rs7480906 | snp | A/G | 0.498346 | 0.0287064 | intron-variant | USP47 | GRCh38.p7 | 11:11921496 | TCATTTCCAGATGCC[A/G]TAGATGAAGTAGCTG | 55031 |
rs7481307 | snp | A/C | 0.478685 | 0.10101 | intron-variant | USP47 | GRCh38.p7 | 11:11917021 | TATCAGTTGTGGTGG[A/C]ATGTGCCTGTGGTCC | 55031 |
rs7483552 | snp | C/G | 0.402454 | 0.198136 | intron-variant | USP47 | GRCh38.p7 | 11:11921622 | AGTGTGCCAGACTTT[C/G]AGAGGAGACATAATC | 55031 |
rs7924430 | snp | A/C | 0.0748431 | 0.178382 | intron-variant | USP47 | GRCh38.p7 | 11:11896148 | AGTACAAAAGATCAT[A/C]GAGTCATATGTGATT | 55031 |
rs7924825 | snp | C/G | 0.0433465 | 0.140692 | upstream-variant-2KB, intron-variant | USP47, LOC107984311 | GRCh38.p7 | 11:11840247 | tcaatccatgataat[C/G]aaaatatcaaaacct | 55031 |
rs7924981 | snp | A/G | 0.499767 | 0.0107802 | intron-variant | USP47 | GRCh38.p7 | 11:11892835 | AAAAAAAAAAAAAAA[A/G]AAAAAGAAAAAAAAA | 55031 |
rs7925746 | snp | A/C | 0.467439 | 0.123371 | intron-variant | USP47 | GRCh38.p7 | 11:11865070 | tcccctaaatacttg[A/C]aaaaatctttctctt | 55031 |
rs7926003 | snp | C/T | 0.148661 | 0.22854 | intron-variant | USP47 | GRCh38.p7 | 11:11873182 | TTTCAAGAGAATATG[C/T]TGATTTCTTTTTATT | 55031 |
rs7926410 | snp | A/G | 0.288127 | 0.247076 | intron-variant | USP47 | GRCh38.p7 | 11:11843597 | ATAAATGTGTATTTC[A/G]TTTTAGAGCTTCATA | 55031 |
rs7927279 | snp | A/G | 0.289683 | 0.24683 | intron-variant | USP47 | GRCh38.p7 | 11:11870714 | ttccttctggcctcc[A/G]tggtttctggtaaga | 55031 |
rs7929007 | snp | A/G | 0 | 0 | intron-variant | USP47 | GRCh38.p7 | 11:11923884 | CATGGCATTCTAGca[A/G]gagttggcaaactat | 55031 |
rs7930136 | snp | A/T | 0.161596 | 0.233848 | intron-variant | USP47 | GRCh38.p7 | 11:11877973 | ACTCTTAGTATTTTT[A/T]AAAAAAGCAAAATTA | 55031 |
rs7931741 | snp | A/G | 0.389903 | 0.207189 | intron-variant, upstream-variant-2KB | USP47 | GRCh38.p7 | 11:11907046 | AAGCTAAATTTTGCT[A/G]TATTAAATCTTATAT | 55031 |
rs7931928 | snp | C/T | 0.0919752 | 0.193722 | intron-variant | USP47 | GRCh38.p7 | 11:11849365 | tctccagaggacatt[C/T]ggcaatgttggggga | 55031 |
rs7932865 | snp | A/G | 0.0437281 | 0.141251 | intron-variant | USP47 | GRCh38.p7 | 11:11945444 | TCTGTACTTAAAATG[A/G]TGGTCCTTAAGATAG | 55031 |
rs7933089 | snp | A/G | 0.431556 | 0.171865 | synonymous-codon | USP47 | GRCh38.p7 | 11:11955081 | CCTTGATATTCATCA[A/G]GATTTAGACTGGAAT | 55031 |
rs7935208 | snp | A/G | 0.0325976 | 0.123435 | intron-variant | USP47 | GRCh38.p7 | 11:11900382 | agccaggatggtctc[A/G]atctcctgacctcgt | 55031 |
rs7935751 | snp | C/T | 0.389715 | 0.207315 | intron-variant | USP47 | GRCh38.p7 | 11:11872474 | cgtagggaagcaagt[C/T]aaagaatttgtggat | 55031 |
rs7936742 | snp | C/T | 0.289683 | 0.24683 | intron-variant | USP47 | GRCh38.p7 | 11:11851104 | TGACACATCTTTTCT[C/T]TTGTGCTGGATTGTT | 55031 |
rs7937824 | snp | A/T | 0.288386 | 0.247035 | intron-variant | USP47 | GRCh38.p7 | 11:11845996 | GTTCTGAGTCTGAGC[A/T]TCCTCAGTTCTTTAA | 55031 |
rs7938839 | snp | G/T | 0.0792508 | 0.182605 | intron-variant | USP47 | GRCh38.p7 | 11:11849295 | ATTTTGCTTTGCTTA[G/T]TTTTCTGTATACTTA | 55031 |
rs7939553 | snp | A/G | 0 | 0 | intron-variant | USP47 | GRCh38.p7 | 11:11928232 | ATTCAAAGCATTTTA[A/G]TTTAATAACATGGGG | 55031 |
rs7939684 | snp | A/G | 0.407674 | 0.194008 | intron-variant | USP47 | GRCh38.p7 | 11:11864611 | gtgtagatatctcat[A/G]tagtatttgtctttg | 55031 |
rs7939855 | snp | A/T | 0.29046 | 0.246704 | intron-variant | USP47 | GRCh38.p7 | 11:11892374 | TTTTCTTTTCTTTTT[A/T]ATTTTCTTTTTTTTT | 55031 |
rs7939856 | snp | A/C | 0.290718 | 0.246662 | intron-variant | USP47 | GRCh38.p7 | 11:11892375 | TTTCTTTTCTTTTTA[A/C]TTTTCTTTTTTTTTT | 55031 |
rs7940058 | snp | A/T | 0 | 0 | intron-variant | USP47 | GRCh38.p7 | 11:11851467 | CCTTAGTTTATTTTT[A/T]TGTTTGTTTGCttta | 55031 |
rs7940553 | snp | A/G | 0.289942 | 0.246789 | intron-variant | USP47 | GRCh38.p7 | 11:11923048 | TTTTTGTACATATAT[A/G]TATATATATATATAT | 55031 |
rs7940860 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | USP47 | GRCh38.p7 | 11:11844191 | TTCTTGCCTCTTCTG[C/T]TGTTCGAATTCTCTG | 55031 |
rs7941549 | snp | C/T | 0.159951 | 0.233219 | intron-variant | USP47 | GRCh38.p7 | 11:11846741 | TTTATTTCTATTGTC[C/T]GACTTCTTATAAAAT | 55031 |
rs7941662 | snp | C/T | 0.0535932 | 0.154675 | intron-variant | USP47 | GRCh38.p7 | 11:11919506 | ATATGAAGTTTCTTA[C/T]TTCTGTTGTAATGCT | 55031 |
rs7942370 | snp | C/T | | | intron-variant | USP47 | GRCh38.p7 | 11:11927958 | TTGCTTTAAAATAGA[C/T]ATATACAATTCTAAT | 55031 |
rs7942523 | snp | C/T | 0 | 0 | intron-variant | USP47 | GRCh38.p7 | 11:11928128 | CAGACTTTTTCTGTG[C/T]TTATTTTTTTTCTAA | 55031 |
rs7945697 | snp | C/T | | | intron-variant | USP47 | GRCh38.p7 | 11:11928429 | CTAATTAACAATATA[C/T]TGTGGTCAGTTTAAA | 55031 |
rs7947202 | snp | A/G | 0.408188 | 0.193589 | intron-variant, upstream-variant-2KB | USP47 | GRCh38.p7 | 11:11906997 | CCATATATACATTTA[A/G]TTTAGTTTTTAACAT | 55031 |
rs7947497 | snp | C/T | | | intron-variant | USP47 | GRCh38.p7 | 11:11923947 | gtttttacATACACT[C/T]tcatttcatctgcaa | 55031 |
rs7947707 | snp | A/T | 0 | 0 | intron-variant | USP47 | GRCh38.p7 | 11:11924066 | gtggtgagggagaac[A/T]tccttaccttgtttc | 55031 |
rs7949831 | snp | A/G | 0.0799831 | 0.183287 | intron-variant | USP47 | GRCh38.p7 | 11:11851351 | GGTTGAAGAGTAGAA[A/G]AGGAGGTCTGGGGAT | 55031 |
rs7951773 | snp | A/G | 0.394354 | 0.204112 | intron-variant | USP47 | GRCh38.p7 | 11:11847002 | AAAGTCAGTATTTTA[A/G]ATATCATTGGAAATG | 55031 |
rs7952289 | snp | A/G | | | intron-variant | USP47 | GRCh38.p7 | 11:11928031 | CATCTAGAAGTTGCT[A/G]CTATTAGAATTTTCC | 55031 |
rs10219228 | snp | A/G | 0.077417 | 0.180873 | utr-variant-3-prime | USP47 | GRCh38.p7 | 11:11958704 | GTACCTGTGTTTCTA[A/G]GGCGGGCACTCAAGG | 55031 |
rs10577564 | in-del | -/TGTGTGTGTG | 0 | 0 | intron-variant | USP47 | GRCh38.p7 | 11:11877850 | GTGTGTGTGTGTGTG[-/TGTGTGTGTG]CGCGCGCGCAGATAA | 55031 |
rs10578253 | in-del | -/ATTAA | | | intron-variant | USP47 | GRCh38.p7 | 11:11946757 | TGACATTTTAAACAA[-/ATTAA]GAGAAATGCTGCCTC | 55031 |
rs10590881 | snp | A/G | 0.458775 | 0.137524 | intron-variant | USP47 | GRCh38.p7 | 11:11877867 | TGTGTGTGCGCGCGC[A/G]CAGATAAGATATTTG | 55031 |
rs10652918 | in-del | -/TT | 0 | 0 | intron-variant | USP47 | GRCh38.p7 | 11:11876264 | TTCATCAGAGAACTC[-/TT]TTGACTAAAAATTTT | 55031 |
rs10670294 | in-del | -/CTC/TCC | 0.5 | 0 | intron-variant | USP47 | GRCh38.p7 | 11:11919052 | CGTTTGGTTTCTTCC[-/CTC/TCC]ACTTGTTTCCTTGTG | 55031 |
rs10741562 | snp | A/G | 0.268452 | 0.249318 | intron-variant | USP47 | GRCh38.p7 | 11:11933239 | CATGATCATTGAACA[A/G]TGTAACCAACTATAC | 55031 |
rs10741563 | snp | C/T | 0.389715 | 0.207315 | intron-variant | USP47 | GRCh38.p7 | 11:11949424 | ATATTTTATCTGGCA[C/T]CTGTTATTTCTCTTA | 55031 |
rs10741564 | snp | A/G | 0.477004 | 0.104734 | intron-variant | USP47 | GRCh38.p7 | 11:11949618 | AGAAGGAAAATACAA[A/G]TGTGTTATCCTATTT | 55031 |
rs10765894 | snp | C/T | 0.391324 | 0.206222 | intron-variant | USP47 | GRCh38.p7 | 11:11884446 | TCTCATAATCTGAAA[C/T]ATTATGTTTTATGTC | 55031 |
rs10765895 | snp | A/G | 0.289165 | 0.246913 | intron-variant | USP47 | GRCh38.p7 | 11:11886388 | AATAGCCAGTTCAGA[A/G]AGGAACATTACTGAC | 55031 |