SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs6687 | snp | C/T | 0.242142 | 0.249883 | utr-variant-3-prime | TRIP12 | GRCh38.p7 | 2:229767552 | TCCATCTTTCCTGAT[C/T]ATAGCAAGAAATGCA | 9320 |
rs10139 | snp | A/G | 0 | 0 | utr-variant-3-prime | TRIP12 | GRCh38.p7 | 2:229767539 | ATTATAGCAAGAAAT[A/G]CAGTGTCTGCCTGTT | 9320 |
rs475316 | snp | A/C | 0.499424 | 0.0169631 | intron-variant | TRIP12 | GRCh38.p7 | 2:229904475 | AAGATTTTAACAATT[A/C]TGGTTAAGTAAATAT | 9320 |
rs475525 | snp | C/T | 0.29789 | 0.24537 | intron-variant | TRIP12 | GRCh38.p7 | 2:229869365 | AATTAACACAATACA[C/T]GCAACTTCGAAATAA | 9320 |
rs476555 | snp | C/G | 0.303438 | 0.244222 | intron-variant | TRIP12 | GRCh38.p7 | 2:229854165 | TAATGTATATTACAG[C/G]CATGAGGTAATTTAT | 9320 |
rs476827 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | TRIP12 | GRCh38.p7 | 2:229889602 | GAAGTAACTAGAAAG[A/G]CTATTGATAAGCTGA | 9320 |
rs479492 | snp | C/T | 0.0482946 | 0.147699 | intron-variant | TRIP12 | GRCh38.p7 | 2:229879854 | TTTGCTTTTAAGTAC[C/T]TGGCTCACAAATCAG | 9320 |
rs480624 | snp | C/T | 0.0383715 | 0.133092 | intron-variant | TRIP12 | GRCh38.p7 | 2:229889168 | GAGTTGTCATCTTCT[C/T]ATGCCTCAGAGATTG | 9320 |
rs485537 | snp | A/T | 0.104149 | 0.203046 | intron-variant | TRIP12 | GRCh38.p7 | 2:229828773 | CTCCATCTCAAAAAA[A/T]ATATATATATATAAA | 9320 |
rs485775 | snp | C/T | 0.0482946 | 0.147699 | intron-variant | TRIP12 | GRCh38.p7 | 2:229828494 | ATGAGCCACTGTGCC[C/T]GGCCTGTTTCCTTGA | 9320 |
rs486305 | snp | C/T | 0 | 0 | intron-variant | TRIP12 | GRCh38.p7 | 2:229907941 | tatactatttttact[C/T]ccattttacagatgg | 9320 |
rs486924 | snp | A/G | 0.0494327 | 0.149241 | intron-variant | TRIP12 | GRCh38.p7 | 2:229820416 | TGGTTTCTCCTCATA[A/G]ATCAGAGGATAAATC | 9320 |
rs488007 | snp | A/G | 0.040671 | 0.13668 | intron-variant | TRIP12 | GRCh38.p7 | 2:229820254 | GAGTTGCCAACCCCA[A/G]TGGTTATAAGACCTC | 9320 |
rs488644 | snp | A/G | 0.296364 | 0.245663 | intron-variant | TRIP12 | GRCh38.p7 | 2:229871965 | tgagaatgttcaggt[A/G]tggcatcatttgcta | 9320 |
rs496982 | snp | G/T | 0.302184 | 0.244493 | intron-variant | TRIP12 | GRCh38.p7 | 2:229824305 | ATGGTATCAAGCTTT[G/T]GAATTTTTACCAAAA | 9320 |
rs503642 | snp | C/G | 0.287085 | 0.247234 | intron-variant | TRIP12 | GRCh38.p7 | 2:229853487 | CAACATGGCAAAACC[C/G]CATCTCTACTAAAAA | 9320 |
rs503926 | snp | G/T | 0.5 | 0.00019968 | intron-variant | TRIP12 | GRCh38.p7 | 2:229823699 | TTGCACTTATttttt[G/T]ttgttgttgttgttt | 9320 |
rs505072 | snp | C/G | 0.0479149 | 0.147179 | intron-variant | TRIP12 | GRCh38.p7 | 2:229868473 | CTCCCAAAGTACTGA[C/G]ATTACAGGCATGAGA | 9320 |
rs508226 | snp | A/T | 0.046775 | 0.145601 | intron-variant | TRIP12 | GRCh38.p7 | 2:229875576 | TCAAGAGGTCTGGAA[A/T]CAAGTCCTGACTACA | 9320 |
rs514666 | snp | C/T | 0.499961 | 0.0043928 | intron-variant | TRIP12 | GRCh38.p7 | 2:229839059 | AACAAGCTAcagtca[C/T]gtgctgcataatgtt | 9320 |
rs517261 | snp | A/G | 0.445724 | 0.155538 | intron-variant | TRIP12 | GRCh38.p7 | 2:229819388 | TCGGCTAATTTTTGT[A/G]TTTTTAGTGGAGATG | 9320 |
rs518255 | snp | C/G | 0.093777 | 0.195178 | intron-variant | TRIP12 | GRCh38.p7 | 2:229819259 | CTGCACCCAGCCTCT[C/G]TAGACTTTATTTTGG | 9320 |
rs519214 | snp | A/G | 0.286303 | 0.24735 | intron-variant | TRIP12 | GRCh38.p7 | 2:229839556 | tggtggcgggcgcct[A/G]tagtcccagctactc | 9320 |
rs519303 | snp | A/T | 0 | 0 | intron-variant | TRIP12 | GRCh38.p7 | 2:229864047 | CACACACACACACAC[A/T]CTCTCTCTCTCTCTC | 9320 |
rs519376 | snp | C/T | 0.48 | 0.0979796 | intron-variant | TRIP12 | GRCh38.p7 | 2:229864004 | TCTCTCTCTCTCTCT[C/T]TCACCCAAATCTTTG | 9320 |
rs525262 | snp | C/T | 0.0479149 | 0.147179 | intron-variant | TRIP12 | GRCh38.p7 | 2:229892820 | gcagtgggctgagat[C/T]gcaccactgcactcc | 9320 |
rs525333 | snp | A/C | 0.0573587 | 0.15934 | intron-variant | TRIP12 | GRCh38.p7 | 2:229843069 | CTCTCTCTCTCCCCC[A/C]CTCCTTCCCTCCCTC | 9320 |
rs526815 | snp | A/G | | | intron-variant | TRIP12 | GRCh38.p7 | 2:229872113 | ATATTGTAAAAAAAA[A/G]AAAAAAAAAAAAAAA | 9320 |
rs533241 | snp | C/T | 0.300673 | 0.244811 | intron-variant | TRIP12 | GRCh38.p7 | 2:229840230 | TCCTGCTACTGTCAA[C/T]AGTATTGTGAAAATA | 9320 |
rs534407 | snp | C/T | 0.49995 | 0.00499176 | intron-variant | TRIP12 | GRCh38.p7 | 2:229884442 | caagaccagcctggc[C/T]aacaagatgaaactc | 9320 |
rs535718 | snp | C/T | 0.0479149 | 0.147179 | intron-variant | TRIP12 | GRCh38.p7 | 2:229827660 | CTATGACAACAATGC[C/T]TTCTTCTGGAATACC | 9320 |
rs537577 | snp | G/T | 0.0479149 | 0.147179 | intron-variant | TRIP12 | GRCh38.p7 | 2:229868095 | TGCAGCAGGCACACA[G/T]GTCTCCACAGCTAAA | 9320 |
rs544480 | snp | C/G | 0.320386 | 0.239895 | synonymous-codon, intron-variant | TRIP12 | GRCh38.p7 | 2:229859061 | TGCCTCTACTTCCTC[C/G]TCGTCTTCTGCTGTA | 9320 |
rs546065 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | TRIP12 | GRCh38.p7 | 2:229896599 | CCTGGGTGACAGAGC[A/G]AGACTCCGTCTCAAA | 9320 |
rs546530 | snp | A/G | 0.499994 | 0.00179711 | intron-variant | TRIP12 | GRCh38.p7 | 2:229888248 | CATTTGCTTATTGAA[A/G]CTCTACCTGGATACC | 9320 |
rs549193 | snp | A/G | 0.499968 | 0.00399348 | intron-variant | TRIP12 | GRCh38.p7 | 2:229843580 | AAACCAAACCAAAAC[A/G]ACAAACAAAAAACAC | 9320 |
rs562948 | snp | A/T | 0.307423 | 0.243316 | intron-variant | TRIP12 | GRCh38.p7 | 2:229827481 | ATTATTATTATTATT[A/T]TTTTGGTTATTAAAC | 9320 |
rs565609 | snp | A/T | 0.0174175 | 0.0916809 | intron-variant | TRIP12 | GRCh38.p7 | 2:229849512 | TCTAGACACTGAAAC[A/T]TCAAAATAATCAGCC | 9320 |
rs566201 | snp | A/G | 0.0471551 | 0.14613 | intron-variant | TRIP12 | GRCh38.p7 | 2:229838910 | CTGTTTACTTATGTC[A/G]CTATTGTAACACCGC | 9320 |
rs575696 | snp | C/T | 0.0663309 | 0.169604 | intron-variant | TRIP12 | GRCh38.p7 | 2:229874252 | TAAACCAAGGAATTC[C/T]TTTTCCCCACAAACT | 9320 |
rs577264 | snp | G/T | 0.0225045 | 0.103662 | intron-variant | TRIP12 | GRCh38.p7 | 2:229831874 | TCAAAGGTTTTTTTT[G/T]TTTGTTTTTTGGGTT | 9320 |
rs581150 | snp | A/C | 0.497329 | 0.0364438 | intron-variant | TRIP12 | GRCh38.p7 | 2:229898974 | TCCCAAAGCATGAGC[A/C]ACTGTGCTCAGTATT | 9320 |
rs722268 | snp | C/T | 0.0659589 | 0.169201 | intron-variant | TRIP12 | GRCh38.p7 | 2:229791017 | TCATTTATTTCTCAA[C/T]TATATTCAAAAATTT | 9320 |
rs831371 | snp | G/T | 0.499994 | 0.00179711 | intron-variant | TRIP12 | GRCh38.p7 | 2:229827154 | tagctgggactacag[G/T]cacgtgccaccacgt | 9320 |
rs831372 | snp | A/T | 0.483418 | 0.0895317 | intron-variant | TRIP12 | GRCh38.p7 | 2:229906397 | ATTTCTGaaaaaaaa[A/T]aaataaataaaaGAC | 9320 |
rs831373 | snp | A/G | 0.29175 | 0.246489 | intron-variant | TRIP12 | GRCh38.p7 | 2:229878971 | CTATTAGAATTCAGC[A/G]gctgagcgcagtgac | 9320 |
rs831374 | snp | C/T | 0.499997 | 0.00119808 | intron-variant | TRIP12 | GRCh38.p7 | 2:229891673 | ACTATTTTTCTAGTA[C/T]CAGCTAGGTTTGACA | 9320 |
rs927594 | snp | G/T | 0.499354 | 0.0179596 | intron-variant | TRIP12 | GRCh38.p7 | 2:229781982 | AACAAGCTCAAAATG[G/T]CTTCACACAGGTTGT | 9320 |
rs1035833 | snp | C/T | 0.40386 | 0.197046 | intron-variant | TRIP12 | GRCh38.p7 | 2:229844482 | AACATGCCTTTAACA[C/T]AGATCATGTAAGAAT | 9320 |
rs1044822 | snp | A/G | 0.21845 | 0.248001 | utr-variant-3-prime | TRIP12 | GRCh38.p7 | 2:229764422 | CTCTACTAGTAAAAT[A/G]ATCAAGCCTTCATTT | 9320 |
rs1054045 | snp | A/C | 0 | 0 | intron-variant | TRIP12 | GRCh38.p7 | 2:229832198 | CATATTTTGCTGACC[A/C]TGTTTTAAACCATAA | 9320 |
rs1372086 | snp | C/T | 0.236434 | 0.249632 | intron-variant | TRIP12 | GRCh38.p7 | 2:229849309 | GCACGCAGGGTTTAT[C/T]GTATCGTGAACATCT | 9320 |
rs1575468 | snp | A/G | 0.499999 | 0.000798721 | intron-variant | TRIP12 | GRCh38.p7 | 2:229789966 | TTGTGTATGGGAGGG[A/G]AAAGTGAAATTTTTA | 9320 |
rs1599843 | snp | C/T | 0.0648419 | 0.167978 | intron-variant | TRIP12 | GRCh38.p7 | 2:229802854 | TCAGTTAACTTCAAG[C/T]GCTACAAAAAGACAA | 9320 |
rs1649129 | snp | A/G | 0 | 0 | intron-variant | TRIP12 | GRCh38.p7 | 2:229865348 | AAAAAAAAAAAGAAA[A/G]AAAGAAAGCAAAATG | 9320 |
rs1660717 | snp | A/G | 0.0479149 | 0.147179 | intron-variant | TRIP12 | GRCh38.p7 | 2:229905375 | CAAAAAGACAAAGTC[A/G]TTTAGGAAGAGAGAA | 9320 |
rs1803846 | snp | C/T | | | stop-gained | TRIP12 | GRCh38.p7 | 2:229768670 | AGTTTTGATAATGAG[C/T]AGCAGAGGTTATTTC | 9320 |
rs2005401 | snp | A/G | 0.0551013 | 0.156571 | intron-variant | TRIP12 | GRCh38.p7 | 2:229900600 | gctgggattacaggc[A/G]tgagctaccgcacct | 9320 |
rs2053461 | snp | A/C | 0.222928 | 0.24853 | intron-variant | TRIP12 | GRCh38.p7 | 2:229847458 | GTGGAGACAGAAGTG[A/C]GTGCATGTGTGTTAA | 9320 |
rs2099794 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TRIP12 | GRCh38.p7 | 2:229811571 | TAACTTTTTAGTGTG[C/T]ACCCACTTAAACATT | 9320 |
rs2162523 | snp | C/T | 0.00396038 | 0.0443227 | intron-variant | TRIP12 | GRCh38.p7 | 2:229894735 | AAGGAACTTCAAATC[C/T]TACTGATCACTTAAC | 9320 |
rs2162525 | snp | A/T | 0 | 0 | intron-variant | TRIP12 | GRCh38.p7 | 2:229861077 | CAAGCACTAAACAAT[A/T]AATAAACCTACATGA | 9320 |
rs2303560 | snp | A/C | 0.119281 | 0.213102 | intron-variant | TRIP12 | GRCh38.p7 | 2:229836785 | TAGCATACTTCCCTC[A/C]CTCTGCCCATCAAAT | 9320 |
rs2433734 | snp | C/T | 0.292523 | 0.246357 | intron-variant | TRIP12 | GRCh38.p7 | 2:229917208 | TATTTTTAGTAGAGA[C/T]GGGGTTTCACCTTGT | 9320 |
rs2433735 | snp | A/G | 0.301177 | 0.244706 | intron-variant | TRIP12 | GRCh38.p7 | 2:229850693 | TCCCTGCAAGCTGAG[A/G]GAGTGGGCTCTGGCC | 9320 |
rs2439569 | snp | A/C | 0.0482946 | 0.147699 | upstream-variant-2KB, intron-variant | TRIP12, FBXO36 | GRCh38.p7 | 2:229922124 | GTCCGCGGGACCGGC[A/C]CCGCTGCCTACTGGC | 9320 |
rs3098730 | snp | C/T | 0 | 0 | intron-variant | TRIP12 | GRCh38.p7 | 2:229855625 | AGCATTTTCTTTTCT[C/T]TTTTTTTTTTTTTTT | 9320 |
rs3215750 | in-del | -/GATTT | 0.417359 | 0.185718 | intron-variant | TRIP12 | GRCh38.p7 | 2:229768856 | AACAGAAACGAATTT[-/GATTT]AAGTACATTGTAATG | 9320 |
rs3791837 | snp | A/G | 0.351635 | 0.228408 | intron-variant | TRIP12 | GRCh38.p7 | 2:229817189 | TGATAATCTCATCAA[A/G]TGGGACAATATGATG | 9320 |
rs3791838 | snp | G/T | 0.0134861 | 0.0810011 | intron-variant | TRIP12 | GRCh38.p7 | 2:229818737 | TATACTTCTGTCTTC[G/T]TAATTGAAAACTTGA | 9320 |
rs3791839 | snp | G/T | 0.350327 | 0.228986 | intron-variant | TRIP12 | GRCh38.p7 | 2:229837922 | TAATAAACCTTTTTT[G/T]CTCCTTCAACAGCGA | 9320 |
rs3796070 | snp | A/G | | | utr-variant-3-prime | TRIP12 | GRCh38.p7 | 2:229764356 | ATTTCCAAACAATTA[A/G]TCTCATTACAGCAGG | 9320 |
rs3796071 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIP12 | GRCh38.p7 | 2:229802723 | TATAAAACTTAATAG[A/G]GTCACAAAGTCCTAT | 9320 |
rs3796072 | snp | C/T | 0.350546 | 0.22889 | intron-variant | TRIP12 | GRCh38.p7 | 2:229802823 | GACAGCCAGAAGGGA[C/T]GGAAAAGACCAAGAA | 9320 |
rs3838549 | in-del | -/TTC | | | intron-variant | TRIP12 | GRCh38.p7 | 2:229844736 | AGTGGATTTAAGATC[-/TTC]ATTCCATAAGTAATT | 9320 |
rs4316932 | snp | C/T | 0.108402 | 0.206034 | intron-variant | TRIP12 | GRCh38.p7 | 2:229809272 | ACTTTATAGAGAAGT[C/T]TGAATACATGGTATG | 9320 |
rs4502396 | snp | A/G | 0 | 0 | intron-variant | TRIP12 | GRCh38.p7 | 2:229794688 | ACAATTCTTTCCTGT[A/G]GCACCTCAAGAGTCC | 9320 |
rs4972913 | snp | C/T | 0.0770779 | 0.182119 | intron-variant | TRIP12 | GRCh38.p7 | 2:229776896 | AGTTGTTGGCACTCA[C/T]GGTGACCTTTAAAAA | 9320 |
rs4972914 | snp | A/G | 0.498832 | 0.0241331 | intron-variant | TRIP12 | GRCh38.p7 | 2:229798075 | TGTAAACAAAGTGTA[A/G]TAATTTTTTGGAACC | 9320 |
rs4972915 | snp | A/G | 0.32973 | 0.236945 | intron-variant | TRIP12 | GRCh38.p7 | 2:229804252 | TAAAAAAAAATATAT[A/G]TGCAATCCTGAAGTG | 9320 |
rs4972916 | snp | C/G | 0.499987 | 0.00259581 | intron-variant | TRIP12 | GRCh38.p7 | 2:229804590 | GTTCTAGAAATGCAC[C/G]ATATTTCACTAAAAG | 9320 |
rs4973228 | snp | G/T | 0.302435 | 0.244439 | intron-variant | TRIP12 | GRCh38.p7 | 2:229792780 | AACTCAACATTCAAG[G/T]AAGCAGTCAACCCCT | 9320 |
rs4973229 | snp | G/T | 0.488732 | 0.074209 | intron-variant | TRIP12 | GRCh38.p7 | 2:229804266 | TGTGCAATCCTGAAG[G/T]GACAGACTTCAGAAA | 9320 |
rs4973230 | snp | A/G | 0.21725 | 0.247846 | intron-variant | TRIP12 | GRCh38.p7 | 2:229833143 | ATATTTTATTCTAAC[A/G]ACTTTCATAATGAAT | 9320 |
rs4973233 | snp | A/T | | | intron-variant | TRIP12 | GRCh38.p7 | 2:229864045 | GAGAGAGAGAGAGAG[A/T]GAGTGTGTGTGTGTG | 9320 |
rs5839348 | in-del | -/T | 0.107694 | 0.205546 | intron-variant | TRIP12 | GRCh38.p7 | 2:229806355 | TTAAACAAAGATAAC[-/T]TTTAAGACTGAAAGG | 9320 |
rs5839349 | in-del | -/C | | | intron-variant | TRIP12 | GRCh38.p7 | 2:229869245 | ATGTTTTCATCATTT[-/C]CAGTAAAAAAGAAAG | 9320 |
rs6436892 | snp | A/T | 0.397271 | 0.202018 | intron-variant | TRIP12 | GRCh38.p7 | 2:229912728 | GATGTTGTGTGCTGT[A/T]GTCGTAAGTTTCAAC | 9320 |
rs6714125 | snp | A/G | 0.409721 | 0.192325 | intron-variant | TRIP12 | GRCh38.p7 | 2:229839058 | GAACAAGCTAcagtc[A/G]tgtgctgcataatgt | 9320 |
rs6716196 | snp | C/T | 0.0689305 | 0.172377 | intron-variant | TRIP12 | GRCh38.p7 | 2:229788233 | CTACACTTAAGTCGA[C/T]AGATCATCTTTAATC | 9320 |
rs6720868 | snp | C/T | 0.433938 | 0.169313 | intron-variant | TRIP12 | GRCh38.p7 | 2:229798860 | AGAAGAAACATAAAA[C/T]TCCCCCCACTTCACC | 9320 |
rs6724938 | snp | C/G | 0.0279526 | 0.114869 | intron-variant | TRIP12 | GRCh38.p7 | 2:229854017 | TACATATAAAATTAT[C/G]CAATTTTATTTGTAT | 9320 |
rs6728584 | snp | C/G | | | intron-variant | TRIP12 | GRCh38.p7 | 2:229800497 | CAACACCTGACATTT[C/G]TATGGAATATACTTA | 9320 |
rs6739819 | snp | C/G | 0.345482 | 0.231048 | intron-variant | TRIP12 | GRCh38.p7 | 2:229903788 | tgggatgccaaagca[C/G]acagatcacttgagc | 9320 |
rs6740255 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | TRIP12 | GRCh38.p7 | 2:229833169 | TGAATATCTCAAACT[A/G]CACTGCCACAAAGAC | 9320 |
rs6749045 | snp | A/C | 0.415563 | 0.18732 | intron-variant | TRIP12 | GRCh38.p7 | 2:229798727 | TTCATAAACTGAGAA[A/C]CTACCTAATTCTTGA | 9320 |
rs6749080 | snp | A/G | 0.344592 | 0.231414 | intron-variant | TRIP12 | GRCh38.p7 | 2:229893844 | tgagtagctgtgagt[A/G]taggtgtgtgccgcc | 9320 |
rs6759000 | snp | A/T | 0.375 | 0.216506 | intron-variant | TRIP12 | GRCh38.p7 | 2:229864049 | GAGAGAGAGAGAGAG[A/T]GTGTGTGTGTGTGTG | 9320 |
rs6759674 | snp | A/T | 0.354019 | 0.227333 | intron-variant | TRIP12 | GRCh38.p7 | 2:229769471 | CCAAAAAAAAAAAAA[A/T]AATAATAAAATAAAA | 9320 |
rs7355661 | snp | C/G | 0.0349115 | 0.127424 | intron-variant, upstream-variant-2KB | TRIP12 | GRCh38.p7 | 2:229881144 | GTACGTTACCTACCT[C/G]AACAGAGTTGTCAGC | 9320 |