SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs1027392 | snp | A/G | 0.436388 | 0.166611 | missense | USP29 | GRCh38.p7 | 19:57129778 | AAATATTTTCTGGCA[A/G]CATGCAGAATGATGC | 57663 |
rs1982911 | snp | A/G | 0.287867 | 0.247116 | upstream-variant-2KB | USP29 | GRCh38.p7 | 19:57119107 | CCCTCGCGCGCCGGG[A/G]CAGGGCCACAAATGA | 57663 |
rs1982912 | snp | A/G | 0.39009 | 0.207062 | upstream-variant-2KB | USP29 | GRCh38.p7 | 19:57119588 | ccaccatgcccggct[A/G]atttttgtattttta | 57663 |
rs1982913 | snp | G/T | 0.267364 | 0.249396 | upstream-variant-2KB | USP29 | GRCh38.p7 | 19:57120015 | GGAGAATCAGGGGAG[G/T]CGGCGCCGGAAGGGG | 57663 |
rs2201524 | snp | G/T | 0.38286 | 0.211774 | downstream-variant-500B | USP29 | GRCh38.p7 | 19:57132087 | acaccagagggatct[G/T]tccggagcatttatt | 57663 |
rs2887657 | snp | A/T | | | upstream-variant-2KB | USP29 | GRCh38.p7 | 19:57118727 | gaatattcatgaaga[A/T]tcttggaaaaaggta | 57663 |
rs3222792 | microsatellite | (CA)26/28/29/30/31/32/33/34 | 0.724688 | 0.179703 | intron-variant | USP29 | GRCh38.p7 | 19:57122516 | AGACCCTCCTTCCAA[(CA)26/28/29/30/31/32/33/34]ATCCCATCACCCAAA | 57663 |
rs3764574 | snp | C/T | 0.499795 | 0.0101216 | synonymous-codon | USP29 | GRCh38.p7 | 19:57130730 | TTCTGGATGTTGAGG[C/T]ACCTCTTGAAGATGA | 57663 |
rs3795003 | snp | C/T | 0.151824 | 0.229916 | missense | USP29 | GRCh38.p7 | 19:57130431 | GGGAATCACTGGATT[C/T]TGAGGTCAGCTTCAT | 57663 |
rs4292020 | snp | A/C | 0.257176 | 0.249897 | intron-variant | USP29 | GRCh38.p7 | 19:57125926 | tttccatatttagtg[A/C]ttcctccaggagctc | 57663 |
rs4293489 | snp | C/G/T | 0.499187 | 0.0201513 | intron-variant | USP29 | GRCh38.p7 | 19:57126071 | aaaattccttaagaa[C/G/T]gttgaatattggccc | 57663 |
rs4293490 | snp | C/T | 0.168135 | 0.236216 | intron-variant | USP29 | GRCh38.p7 | 19:57126161 | cctttgtgggtaacc[C/T]gacctttctctctgg | 57663 |
rs4408638 | snp | A/G | 0.284471 | 0.247612 | intron-variant | USP29 | GRCh38.p7 | 19:57125934 | tttagtgcttcctcc[A/G]ggagctcttgtaagg | 57663 |
rs4456615 | snp | A/G | 0.168135 | 0.236216 | intron-variant | USP29 | GRCh38.p7 | 19:57126153 | tgggcttccctttgt[A/G]ggtaacccgaccttt | 57663 |
rs4801430 | snp | G/T | | | intron-variant | USP29 | GRCh38.p7 | 19:57124491 | TTGGTTTTCTTTTTT[G/T]TTTTTTTTTTGTTTT | 57663 |
rs4801431 | snp | C/T | 0.489318 | 0.0722982 | intron-variant | USP29 | GRCh38.p7 | 19:57125736 | tgccagtctgtatct[C/T]ttaattgggggcatt | 57663 |
rs8103779 | snp | A/G | 0.383824 | 0.211166 | utr-variant-3-prime | USP29 | GRCh38.p7 | 19:57131683 | TCTTCACGTTTTGAc[A/G]gtggttttcaaaatg | 57663 |
rs8103793 | snp | A/G | 0.44546 | 0.155869 | utr-variant-3-prime | USP29 | GRCh38.p7 | 19:57131731 | acagcaacagctagg[A/G]actgattagaaatgc | 57663 |
rs8104446 | snp | A/T | 0.0498117 | 0.149749 | utr-variant-3-prime | USP29 | GRCh38.p7 | 19:57131738 | cagctagggactgat[A/T]agaaatgcaaattct | 57663 |
rs9973206 | snp | A/C | 0.193786 | 0.243598 | stop-gained | USP29 | GRCh38.p7 | 19:57131414 | CCCTCAGGGGGAATA[A/C]GAAGGTGACTCTTTG | 57663 |
rs10409534 | snp | A/G | 0.0444908 | 0.142359 | intron-variant | USP29 | GRCh38.p7 | 19:57120350 | aaaaatttaaaaatt[A/G]cccacgcctgtagtg | 57663 |
rs10414335 | snp | G/T | 0.325327 | 0.238382 | intron-variant | USP29 | GRCh38.p7 | 19:57123538 | TCAGCCTTAGTGTTA[G/T]AAAAGCAGTAAGCGG | 57663 |
rs10418306 | snp | C/T | | | intron-variant | USP29 | GRCh38.p7 | 19:57120674 | tgcctgtaatcccag[C/T]tactggggaggctga | 57663 |
rs10418765 | snp | G/T | 0.0341408 | 0.126114 | intron-variant | USP29 | GRCh38.p7 | 19:57127946 | cctgatctgcagatt[G/T]caaaaactgtgggaa | 57663 |
rs10423431 | snp | C/G | 0.433382 | 0.169915 | intron-variant | USP29 | GRCh38.p7 | 19:57125289 | ggagtgttttacttc[C/G]aattatgtggtcaat | 57663 |
rs10423441 | snp | A/G | 0.487558 | 0.0778863 | intron-variant | USP29 | GRCh38.p7 | 19:57125298 | tacttcgaattatgt[A/G]gtcaattttaaaata | 57663 |
rs10424390 | snp | C/T | 0.0383715 | 0.133092 | intron-variant | USP29 | GRCh38.p7 | 19:57125169 | GCCAGGCtttccatg[C/T]agttgtgtggttttt | 57663 |
rs10426755 | snp | C/T | 0.0399052 | 0.1355 | intron-variant | USP29 | GRCh38.p7 | 19:57122222 | AAGTTAATCAAGAAA[C/T]GTATTTCCTGGAAAA | 57663 |
rs11669447 | snp | A/G | 0 | 0 | intron-variant | USP29 | GRCh38.p7 | 19:57121613 | atatatgttatatat[A/G]cttatatgtatgtta | 57663 |
rs12610100 | snp | C/T | 0.271702 | 0.249056 | intron-variant | USP29 | GRCh38.p7 | 19:57125604 | tccttttttttgctt[C/T]ccatttgcttggcaa | 57663 |
rs12611179 | snp | C/T | | | intron-variant | USP29 | GRCh38.p7 | 19:57125194 | gtttttagtgagttt[C/T]ttaatcctgagttat | 57663 |
rs12974694 | snp | A/G | 0.48978 | 0.0707512 | intron-variant | USP29 | GRCh38.p7 | 19:57126257 | tgctcttctcgagga[A/G]tatctttgtggtatt | 57663 |
rs12975737 | snp | C/T | | | intron-variant | USP29 | GRCh38.p7 | 19:57120620 | ggtgaaaccctgtct[C/T]tactaaaaatacaaa | 57663 |
rs12979911 | snp | A/C | 0 | 0 | upstream-variant-2KB | USP29 | GRCh38.p7 | 19:57119916 | CGGCCACGCTAGAGC[A/C]CGTACCTAGACCCGT | 57663 |
rs12980671 | snp | A/G | 0.453575 | 0.145111 | intron-variant | USP29 | GRCh38.p7 | 19:57120288 | TAGCTAGCTGAGATC[A/G]TGCCACTGCACTCCA | 57663 |
rs16987751 | snp | A/G | 0.0498117 | 0.149749 | intron-variant | USP29 | GRCh38.p7 | 19:57123716 | ACCCATAAAGTATAA[A/G]GTTTCTCAAACAACA | 57663 |
rs17239802 | snp | A/G | 0.271702 | 0.249056 | intron-variant | USP29 | GRCh38.p7 | 19:57123831 | TAATTGGGGAGGGGC[A/G]CTTTTAGGAATGCAT | 57663 |
rs28371409 | snp | A/C | 0.0356815 | 0.128715 | intron-variant | USP29 | GRCh38.p7 | 19:57121093 | GAGTGAGACTCCATC[A/C]CCGCTCCGCTCCCTC | 57663 |
rs28796125 | snp | A/G | 0.16846 | 0.236329 | intron-variant | USP29 | GRCh38.p7 | 19:57126224 | CTTGGAGAATCTGAC[A/G]ATTATGTGTCTTGGG | 57663 |
rs28841103 | snp | C/T | 0.168785 | 0.236441 | intron-variant | USP29 | GRCh38.p7 | 19:57126410 | AATCAATCGTAGGTT[C/T]GGTCTTTTCACATAG | 57663 |
rs34124799 | in-del | -/C | 0.482683 | 0.0914256 | intron-variant | USP29 | GRCh38.p7 | 19:57128058 | CCAGGTGAGGCAATG[-/C]CCCCACCCTGCTTCT | 57663 |
rs34233382 | snp | A/G | 0.00172986 | 0.0293588 | missense | USP29 | GRCh38.p7 | 19:57129928 | GTAGTGCTGCCACCA[A/G]AGTGTTTGTTTGCCC | 57663 |
rs34378601 | snp | A/C | 0.404209 | 0.196773 | intron-variant | USP29 | GRCh38.p7 | 19:57121357 | TTATATATGTTATAT[A/C]TACTTATGTTATATA | 57663 |
rs34399911 | in-del | -/T | 0.5 | 0 | intron-variant | USP29 | GRCh38.p7 | 19:57124468 | CTGTTTTTTGTGGGG[-/T]TTTTTTTTTGGTTTT | 57663 |
rs34650239 | snp | C/T | 0.486464 | 0.0811471 | intron-variant | USP29 | GRCh38.p7 | 19:57121017 | GGAGAATCACTTGAA[C/T]CCAGGAAGCAGAGGC | 57663 |
rs34667035 | in-del | -/A | | | intron-variant | USP29 | GRCh38.p7 | 19:57126810 | TCCTTGCTGAACAGG[-/A]AGTTGCGATCATTTG | 57663 |
rs34833540 | in-del | -/A | | | intron-variant | USP29 | GRCh38.p7 | 19:57125134 | CAGCCTTAGTGTTAC[-/A]AAAAGCAGTAAGTGG | 57663 |
rs34946355 | snp | C/T | 0.453209 | 0.145623 | intron-variant | USP29 | GRCh38.p7 | 19:57121466 | TTATATATACTTATA[C/T]ATGTTATACATACTT | 57663 |
rs35009834 | in-del | -/TA | 0.486464 | 0.0811471 | intron-variant | USP29 | GRCh38.p7 | 19:57121430 | TATGTTATATATACT[-/TA]TGTTATATACTTATA | 57663 |
rs35123282 | in-del | -/A | | | intron-variant | USP29 | GRCh38.p7 | 19:57121556 | ATGCTATGTATACTT[-/A]TATATGTTATATATA | 57663 |
rs35185322 | in-del | -/T | | | intron-variant | USP29 | GRCh38.p7 | 19:57121554 | ATATGCTATGTATAC[-/T]TATATATGTTATATA | 57663 |
rs35338518 | in-del | -/ATAG | 0.385741 | 0.209939 | intron-variant | USP29 | GRCh38.p7 | 19:57121953 | TGTCTCTATTAAAAA[-/ATAG]ATAGATAGATAGATA | 57663 |
rs35394887 | snp | A/C | 0.0117986 | 0.0758953 | missense | USP29 | GRCh38.p7 | 19:57131045 | GGCACTGGGTTCTGA[A/C]AACCCAGGAAACAAA | 57663 |
rs35436572 | snp | C/T | 0.00530037 | 0.0512064 | missense | USP29 | GRCh38.p7 | 19:57130591 | ACTTTAGAGATAGGG[C/T]AATCGGTGAAAAGGA | 57663 |
rs35629721 | in-del | -/A | | | frameshift-variant | USP29 | GRCh38.p7 | 19:57129325 | GTTTAGAGGATTTAG[-/A]AAAAGATAGAGATTT | 57663 |
rs35663514 | snp | C/T | 1.64955e-05 | 0.00287184 | synonymous-codon | USP29 | GRCh38.p7 | 19:57130457 | TTCCCTGGTTCTACC[C/T]GTTGAACCAGACAAG | 57663 |
rs35717160 | in-del | -/G | | | frameshift-variant | USP29 | GRCh38.p7 | 19:57129633 | CTCAAGGTGTCCCAT[-/G]GGGAATATATTCCCT | 57663 |
rs35732035 | snp | A/G | 0.0195095 | 0.0968201 | synonymous-codon | USP29 | GRCh38.p7 | 19:57129296 | TATACAAAGCAATAG[A/G]AAGAACCCATCAAGT | 57663 |
rs35825687 | snp | C/T | 0.221141 | 0.248329 | intron-variant | USP29 | GRCh38.p7 | 19:57121758 | ATAAAACAAAAAGCA[C/T]GGTTACTACAAAGAA | 57663 |
rs57441095 | snp | C/T | 0.0633504 | 0.166319 | upstream-variant-2KB | USP29 | GRCh38.p7 | 19:57119340 | GGTGGCTGAGGCAAA[C/T]ACGCTTGAAGGCCTA | 57663 |
rs57785203 | in-del | -/TT | 0.380138 | 0.213458 | intron-variant | USP29 | GRCh38.p7 | 19:57124468 | CTGTTTTTTGTGGGG[-/TT]TTTTTTTTGGTTTTC | 57663 |
rs57908333 | snp | A/C | 0.272511 | 0.248984 | intron-variant | USP29 | GRCh38.p7 | 19:57126821 | ACAGGAGTTGCGATC[A/C]TTTGGAGAAGAGACA | 57663 |
rs59382095 | snp | C/T | 0.0490535 | 0.14873 | upstream-variant-2KB | USP29 | GRCh38.p7 | 19:57119820 | GGTAACAGGATGAAC[C/T]CGCCCCTGGGCTGGT | 57663 |
rs60292265 | snp | A/G | 0.220246 | 0.248223 | downstream-variant-500B | USP29 | GRCh38.p7 | 19:57132043 | TTCTGAGATCGGGCC[A/G]GTTGGGATTCCAAAG | 57663 |
rs60332357 | in-del | -/A | | | intron-variant | USP29 | GRCh38.p7 | 19:57123210 | TTAAATGTAATAAAA[-/A]TTGAATATCATATGG | 57663 |
rs60692365 | in-del | -/GATA | 0.5 | 0 | intron-variant | USP29 | GRCh38.p7 | 19:57121976 | ATAGATAGATAGATA[-/GATA]CATAGAACATCAAAA | 57663 |
rs61735238 | snp | G/T | 0.00376118 | 0.0432024 | missense | USP29 | GRCh38.p7 | 19:57130874 | AGGAATGGCTGAACA[G/T]CTCCAGCAGTGTATT | 57663 |
rs61735239 | snp | A/T | 0.00102476 | 0.0226126 | missense | USP29 | GRCh38.p7 | 19:57131102 | AGGTGAAGCCAAGGA[A/T]CTAACAAGAAACGTG | 57663 |
rs61735240 | snp | A/G | 0.0180775 | 0.0933379 | synonymous-codon | USP29 | GRCh38.p7 | 19:57131291 | CAAAATGCAGGAGGC[A/G]AGGCTTCACTCTGGG | 57663 |
rs61757571 | snp | C/T | 0.0135473 | 0.0811796 | synonymous-codon | USP29 | GRCh38.p7 | 19:57131207 | CCATTACATCAGCGA[C/T]GTGTATGACTTTCAG | 57663 |
rs62134268 | snp | C/T | 0.489492 | 0.0717183 | intron-variant | USP29 | GRCh38.p7 | 19:57126391 | CGTCACTTTCAGGTA[C/T]ACCAATCAATCGTAG | 57663 |
rs71186224 | in-del | -/AC | 0 | 0 | intron-variant | USP29 | GRCh38.p7 | 19:57122556 | CACTCACACACACAT[-/AC]ACACACACACACACA | 57663 |
rs71186225 | in-del | -/A | 0 | 0 | intron-variant | USP29 | GRCh38.p7 | 19:57124492 | AAAACAAAAAAAAAA[-/A]CAAAAAAGAAAACCA | 57663 |
rs71293954 | in-del | -/TTT | 0.5 | 0 | intron-variant | USP29 | GRCh38.p7 | 19:57120813 | CCGGCCTTTTTTCTG[-/TTT]TTTTTTTTTTTTTTT | 57663 |
rs73623808 | snp | A/T | 0.170084 | 0.236883 | intron-variant | USP29 | GRCh38.p7 | 19:57121258 | AATGTAGGATATATA[A/T]GTTATATATATACTT | 57663 |
rs74179414 | in-del | -/AT | 0.5 | 0 | intron-variant | USP29 | GRCh38.p7 | 19:57121431 | ATGTTATATATACTT[-/AT]GTTATATACTTATAT | 57663 |
rs74511605 | snp | A/G | 0.00178015 | 0.029781 | missense | USP29 | GRCh38.p7 | 19:57130519 | GTGGAGATGCAAGCC[A/G]AGAGCAGCATCAGAG | 57663 |
rs74633963 | snp | C/G | 0.021333 | 0.101051 | intron-variant | USP29 | GRCh38.p7 | 19:57122578 | GTGTGAGTGTTGGAA[C/G]GAGGGTCTGTCTAAA | 57663 |
rs74873332 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | USP29 | GRCh38.p7 | 19:57121976 | ATAGATAGATAGATA[C/G]ATACATAGAACATCA | 57663 |
rs74893436 | snp | A/G | 0.136506 | 0.222754 | intron-variant | USP29 | GRCh38.p7 | 19:57123604 | ACAATGTGTGATCTC[A/G]ATGCATCCTCTCTGT | 57663 |
rs75108927 | snp | C/T | 0.000626752 | 0.0176913 | missense | USP29 | GRCh38.p7 | 19:57130140 | TATAACTGTCAGATG[C/T]GTAAGCAGAAGAGTT | 57663 |
rs75587245 | snp | A/C | 0.5 | 0 | downstream-variant-500B | USP29 | GRCh38.p7 | 19:57132290 | AGACCCTGTCTCTAC[A/C]AAAAATAATTCAGCA | 57663 |
rs76615047 | snp | A/C/T | 0.0178257 | 0.0928375 | upstream-variant-2KB | USP29 | GRCh38.p7 | 19:57118271 | GAGGCAGGGCTCCAA[A/C/T]CCACGCAGCCTTGCT | 57663 |
rs76777014 | snp | C/G | 0.039522 | 0.134904 | upstream-variant-2KB | USP29 | GRCh38.p7 | 19:57118375 | TGGTCCCAATGCAGT[C/G]TCCTTATAGGCACAA | 57663 |
rs77031816 | snp | C/T | 0.00358779 | 0.0422022 | upstream-variant-2KB | USP29 | GRCh38.p7 | 19:57120016 | GAGAATCAGGGGAGT[C/T]GGCGCCGGAAGGGGC | 57663 |
rs77239938 | snp | G/T | 0.0360663 | 0.129354 | intron-variant | USP29 | GRCh38.p7 | 19:57124497 | TTCTTTTTTGTTTTT[G/T]TTTTGTTTTTGTTTT | 57663 |
rs77420930 | snp | C/G | 0.133093 | 0.220981 | intron-variant | USP29 | GRCh38.p7 | 19:57127854 | CTCTTGCAACTAGCT[C/G]GGTGTCTCCCCGAAC | 57663 |
rs77731254 | in-del | -/A | 0.275197 | 0.248727 | intron-variant | USP29 | GRCh38.p7 | 19:57121119 | CCCTCACCTCCCGCC[-/A]AAAAAAAAAAAGAAA | 57663 |
rs78060505 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | USP29 | GRCh38.p7 | 19:57127852 | AACTCTTGCAACTAG[C/T]TCGGTGTCTCCCCGA | 57663 |
rs78216816 | snp | G/T | 0.221439 | 0.248363 | intron-variant | USP29 | GRCh38.p7 | 19:57128258 | AAAAAATTTTATGTA[G/T]CGATGAGGTCTCCCT | 57663 |
rs78231659 | snp | C/G | 0.039522 | 0.134904 | upstream-variant-2KB | USP29 | GRCh38.p7 | 19:57118518 | TAGGGGCGGATAAGA[C/G]TCTGAAAACCAGGGT | 57663 |
rs78705001 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | USP29 | GRCh38.p7 | 19:57131853 | GAAGAACACTGGTAA[C/T]GTGTGGAGTATCTTG | 57663 |
rs78710038 | snp | C/T | 0.0441095 | 0.141807 | upstream-variant-2KB | USP29 | GRCh38.p7 | 19:57118813 | GCTCTGTGGTATGCC[C/T]GCACTTTTCTTTCTT | 57663 |
rs79709876 | in-del | -/T | | | intron-variant | USP29 | GRCh38.p7 | 19:57124477 | GTGGGGTTTTTTTTT[-/T]GGTTTTCTTTTTTGT | 57663 |
rs80212391 | snp | C/T | 0.242775 | 0.249896 | intron-variant | USP29 | GRCh38.p7 | 19:57121095 | GTGAGACTCCATCCC[C/T]GCTCCGCTCCCTCAC | 57663 |
rs111279534 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | USP29 | GRCh38.p7 | 19:57121911 | TGGAGGTCAGGAGTT[C/T]GAGACCTGGGCAACA | 57663 |
rs111397088 | snp | C/T | 0.5 | 0 | synonymous-codon | USP29 | GRCh38.p7 | 19:57131027 | TGACCTGAATCACCT[C/T]GGGGCACTGGGTTCT | 57663 |
rs111778303 | snp | C/T | 0.000922372 | 0.0214554 | synonymous-codon | USP29 | GRCh38.p7 | 19:57130301 | ATCTTCTTATTGCAA[C/T]GAAAGCACCAAACCA | 57663 |
rs111970708 | snp | A/C | 0.5 | 0 | upstream-variant-2KB | USP29 | GRCh38.p7 | 19:57120039 | GAAGGGGCGGGTCCG[A/C]GCTGAGATTTCCAGA | 57663 |
rs112129113 | snp | A/G | 0.5 | 0 | intron-variant | USP29 | GRCh38.p7 | 19:57122242 | TTCCTGGAAAAACCC[A/G]TGATATGGGTGGAGC | 57663 |