SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs13987 | snp | A/G | 0.362313 | 0.223351 | utr-variant-3-prime, downstream-variant-500B | MARK3 | GRCh38.p7 | 14:103503572 | TGGCAGCCAGTCATT[A/G]CTAGTACCTCTGCGG | 4140 |
rs911556 | snp | C/T | 0.0607341 | 0.163335 | intron-variant | MARK3 | GRCh38.p7 | 14:103489158 | AGATGTCGTCATCTC[C/T]ATGAAGTGTTATCTG | 4140 |
rs911557 | snp | A/C | 0 | 0 | intron-variant | MARK3 | GRCh38.p7 | 14:103481568 | CCATAATCTTACAGA[A/C]CAAATGTTACTCCTC | 4140 |
rs911558 | snp | A/G | 0 | 0 | intron-variant | MARK3 | GRCh38.p7 | 14:103481550 | AATGTTACTCCTCAT[A/G]TCAACTCTTACCTAA | 4140 |
rs962230 | snp | C/T | 0.0322114 | 0.122752 | intron-variant | MARK3 | GRCh38.p7 | 14:103391200 | TGGAAGGCTGTCCTA[C/T]GTACTGTAAAATGTT | 4140 |
rs975891 | snp | A/T | | | intron-variant | MARK3 | GRCh38.p7 | 14:103417348 | GCTCACTCAATCTAG[A/T]ACTCTAATAACTGTT | 4140 |
rs975892 | snp | A/T | 0.487305 | 0.0786545 | intron-variant | MARK3 | GRCh38.p7 | 14:103417012 | gcctggcaattctat[A/T]acatttctctagtcc | 4140 |
rs1013650 | snp | C/T | 0.417034 | 0.18601 | intron-variant | MARK3 | GRCh38.p7 | 14:103442866 | TTAGCTTTACTGACT[C/T]CTTACATTATTATTT | 4140 |
rs1028613 | snp | C/T | 0.330249 | 0.23677 | intron-variant | MARK3 | GRCh38.p7 | 14:103421987 | ggccatcctgggaga[C/T]aaggaAACCAGTGAG | 4140 |
rs1058545 | snp | C/G | 0.00527701 | 0.0510946 | missense | MARK3 | GRCh38.p7 | 14:103475095 | CCTCCCGGAAATCAA[C/G]TGGCAGTGCTGTTGG | 4140 |
rs1058546 | snp | A/C | 0 | 0 | missense | MARK3 | GRCh38.p7 | 14:103480451 | GTGAGAGAACTACAG[A/C]TGATAGACACTCAGT | 4140 |
rs1058681 | snp | G/T | | | utr-variant-3-prime | MARK3 | GRCh38.p7 | 14:103503259 | TAAATTAAGTAGCAA[G/T]TAAAGTGTTTTCCTG | 4140 |
rs1107070 | snp | G/T | 0.487368 | 0.0784625 | downstream-variant-500B | MARK3 | GRCh38.p7 | 14:103504171 | AGACCTGCAGCTTTT[G/T]TCCAACACCTACATG | 4140 |
rs1116095 | snp | C/T | 0.455273 | 0.142699 | intron-variant | MARK3 | GRCh38.p7 | 14:103465542 | CCTAGAGGGAAAACA[C/T]CAAGACAAAAATGAA | 4140 |
rs1138399 | snp | A/G | 0 | 0 | intron-variant | MARK3 | GRCh38.p7 | 14:103490436 | acacttataatccca[A/G]cactttggaaggcca | 4140 |
rs1138400 | snp | A/G | 0.49655 | 0.04139 | intron-variant | MARK3 | GRCh38.p7 | 14:103490496 | TTAAGACCAGCCTGG[A/G]TAATATAGCGAGACC | 4140 |
rs1804931 | snp | G/T | | | missense, intron-variant | MARK3 | GRCh38.p7 | 14:103491863 | TCCGCTTCCCAAGAG[G/T]CACTGCCAGTCGTAG | 4140 |
rs1951389 | snp | C/G | 0.361474 | 0.223771 | intron-variant | MARK3 | GRCh38.p7 | 14:103432188 | GCTTTACTACTGGGT[C/G]AGCAGTATCAACTTG | 4140 |
rs1951390 | snp | A/G | 0.0310518 | 0.120672 | intron-variant | MARK3 | GRCh38.p7 | 14:103431983 | ACAAATTCAGGTGGG[A/G]GGGGGGAAACAATTC | 4140 |
rs1951391 | snp | A/G | 0.414576 | 0.188188 | intron-variant | MARK3 | GRCh38.p7 | 14:103431976 | CAGGTGGGAGGGGGG[A/G]AACAATTCCAAGTAT | 4140 |
rs1951392 | snp | A/C | 0.332106 | 0.236133 | intron-variant | MARK3 | GRCh38.p7 | 14:103387030 | CTAGATGTTTTACAG[A/C]ATATAGTCAACAACT | 4140 |
rs1951393 | snp | A/G | 0.0711525 | 0.174681 | intron-variant | MARK3 | GRCh38.p7 | 14:103466551 | ATAAACTGTTCATAT[A/G]ACTTGTGCTTAACTT | 4140 |
rs1961600 | snp | C/T | 0.331874 | 0.236213 | intron-variant | MARK3 | GRCh38.p7 | 14:103395807 | TCTCTCTCTCCAAAT[C/T]GGAGTGTCAGATGCT | 4140 |
rs1989565 | snp | A/G | 0.406296 | 0.19512 | intron-variant | MARK3 | GRCh38.p7 | 14:103395856 | CTTATTTTTCTGTTT[A/G]TTTAAGGCTGATTGG | 4140 |
rs2010281 | snp | A/G | 0.332106 | 0.236133 | intron-variant | MARK3 | GRCh38.p7 | 14:103395985 | GGCCTAGGCAAGCAC[A/G]GAATGCCCATGTTCC | 4140 |
rs2065013 | snp | C/G | 0.0659589 | 0.169201 | intron-variant | MARK3 | GRCh38.p7 | 14:103438113 | CTCGGGAGGCTGAGG[C/G]AGGGGAATCACTTGA | 4140 |
rs2065014 | snp | G/T | 0.0644693 | 0.167566 | intron-variant | MARK3 | GRCh38.p7 | 14:103438074 | GGTGGAGGTTGCGGT[G/T]AGCCGAGATCACGCC | 4140 |
rs2065015 | snp | A/C | 0.361474 | 0.223771 | intron-variant | MARK3 | GRCh38.p7 | 14:103437724 | CTCTCACAAAGGCCT[A/C]ATTTGCACCCAAGTT | 4140 |
rs2065016 | snp | A/T | 0.365439 | 0.221752 | intron-variant, upstream-variant-2KB | MARK3 | GRCh38.p7 | 14:103413319 | TCTTGAGGAAAAAAA[A/T]GTTCCATTTACATTA | 4140 |
rs2065017 | snp | A/G | 0.362313 | 0.223351 | intron-variant, upstream-variant-2KB | MARK3 | GRCh38.p7 | 14:103413242 | TATAAAACATAGATG[A/G]AAAAAGTTACAAAAC | 4140 |
rs2065018 | snp | A/G | 0.362313 | 0.223351 | intron-variant, upstream-variant-2KB | MARK3 | GRCh38.p7 | 14:103412850 | AAAGAAAGACTTGGC[A/G]TCATTAAAATATCAA | 4140 |
rs2065019 | snp | C/T | 0.0298908 | 0.118541 | intron-variant | MARK3 | GRCh38.p7 | 14:103408680 | TATTTACAGGGCACA[C/T]TGCTGCAAACAGAGG | 4140 |
rs2065020 | snp | A/G | 0.0644693 | 0.167566 | intron-variant | MARK3 | GRCh38.p7 | 14:103405386 | tccagcctgggtgac[A/G]gagcgagactccatc | 4140 |
rs2145856 | snp | C/T | 0 | 0 | intron-variant | MARK3 | GRCh38.p7 | 14:103409574 | CAAGGAACTTACTTT[C/T]TACATAATGAATTTC | 4140 |
rs2145858 | snp | A/G | 0.0614824 | 0.164198 | intron-variant | MARK3 | GRCh38.p7 | 14:103472571 | caagctccacctccc[A/G]ggttcacgccattct | 4140 |
rs2180992 | snp | A/G | 0.0715223 | 0.175059 | intron-variant | MARK3 | GRCh38.p7 | 14:103437617 | CTAAAATAGCATAAT[A/G]AGTCCTTGGTACAAT | 4140 |
rs2273699 | snp | C/T | 0.435376 | 0.167738 | intron-variant | MARK3 | GRCh38.p7 | 14:103457138 | CAAATACTTCACCTA[C/T]AGGTGAGAGAAATAA | 4140 |
rs2273700 | snp | C/T | 0.32955 | 0.237006 | intron-variant | MARK3 | GRCh38.p7 | 14:103457077 | AATTTTCCCATAAAT[C/T]GATGTTTCACTTTTA | 4140 |
rs2273701 | snp | A/C | 0.487495 | 0.0780784 | intron-variant | MARK3 | GRCh38.p7 | 14:103456888 | TCTTATTTTAAAGAG[A/C]GTTTTCAATAGGCTT | 4140 |
rs2273702 | snp | C/G | 0.497416 | 0.0358495 | intron-variant | MARK3 | GRCh38.p7 | 14:103451845 | ATGCACATATAAACT[C/G]TAACTATGAAAAGCA | 4140 |
rs2273703 | snp | C/G | 0.416708 | 0.186302 | intron-variant | MARK3 | GRCh38.p7 | 14:103451692 | CTGAATGTTCAGTGT[C/G]ACTTCCATATGTGCT | 4140 |
rs2403173 | snp | C/T | 0.417034 | 0.18601 | intron-variant | MARK3 | GRCh38.p7 | 14:103442952 | GTGTCCCCCCCCCCC[C/T]CCCACCGACAAGGAA | 4140 |
rs2403174 | snp | A/G | 0.487558 | 0.0778863 | intron-variant | MARK3 | GRCh38.p7 | 14:103455640 | GGCTGAGGCACGAGA[A/G]TTGCTTGAACGTTGG | 4140 |
rs2403175 | snp | G/T | 0.0799831 | 0.183287 | intron-variant | MARK3 | GRCh38.p7 | 14:103462720 | ACAGCCAAACAAATG[G/T]GGGCCTCCAGAAATG | 4140 |
rs2403176 | snp | A/T | 0 | 0 | intron-variant | MARK3 | GRCh38.p7 | 14:103473494 | GTTCACAATGTCAGT[A/T]GACGTCTCATGGTAT | 4140 |
rs2403180 | snp | A/G | 0.332799 | 0.23589 | intron-variant | MARK3 | GRCh38.p7 | 14:103482289 | actctgggaggccaa[A/G]gcaggtggatcactt | 4140 |
rs2403181 | snp | A/T | 0.0648419 | 0.167978 | intron-variant | MARK3 | GRCh38.p7 | 14:103482320 | gaggtcaggagttcg[A/T]gaccagcctggccaa | 4140 |
rs2756130 | snp | A/G | 0.0603597 | 0.1629 | utr-variant-3-prime, downstream-variant-500B | MARK3 | GRCh38.p7 | 14:103503462 | GAGATGGGGCCACAC[A/G]CCGACTCTCAGGGTA | 4140 |
rs2756131 | snp | C/G | 0.0633504 | 0.166319 | intron-variant | MARK3 | GRCh38.p7 | 14:103502525 | TCAGGGAAGGAGTTG[C/G]CAGCCAGCTCCTGCC | 4140 |
rs2756132 | snp | C/G | 0.481473 | 0.0944461 | intron-variant | MARK3 | GRCh38.p7 | 14:103501483 | AGGATGTGTCTGTGG[C/G]ATAATAAAGTACACA | 4140 |
rs2756133 | snp | A/G | 0.0759472 | 0.179459 | intron-variant | MARK3 | GRCh38.p7 | 14:103498020 | CATGTTGGCCAGTCT[A/G]GTCTCGAACTCCTGG | 4140 |
rs2756134 | snp | A/G | 0.0244538 | 0.107838 | intron-variant | MARK3 | GRCh38.p7 | 14:103497570 | TTTTACTTTTATGTA[A/G]TAAACACGAAGAATT | 4140 |
rs2756135 | snp | C/T | 0.487368 | 0.0784625 | intron-variant | MARK3 | GRCh38.p7 | 14:103496242 | ATTACTATAGAAGTG[C/T]TTTTCTTAACTTTTC | 4140 |
rs2756136 | snp | C/T | | | intron-variant | MARK3 | GRCh38.p7 | 14:103493566 | GTTTATTCTGGGAGT[C/T]ACCAGACTCTTCTCA | 4140 |
rs2756137 | snp | C/T | 0.0629771 | 0.165899 | intron-variant | MARK3 | GRCh38.p7 | 14:103493396 | ATAGAAACCTTCTGA[C/T]GCGTCTGACTTCTAG | 4140 |
rs2765052 | snp | A/C | 0 | 0 | intron-variant | MARK3 | GRCh38.p7 | 14:103501798 | ATACTAAATGGGTTA[A/C]AAAGATAAGCAAAAG | 4140 |
rs2765053 | snp | A/G | 0.0599851 | 0.162463 | intron-variant | MARK3 | GRCh38.p7 | 14:103494712 | aaggcgaagattgcc[A/G]tgggctgagatcatg | 4140 |
rs2896484 | snp | A/T | 0 | 0 | intron-variant | MARK3 | GRCh38.p7 | 14:103432467 | ccttatcgtgattgt[A/T]aaatagggcaacact | 4140 |
rs2896486 | snp | A/T | | | intron-variant | MARK3 | GRCh38.p7 | 14:103484769 | aaccctgtctaaaat[A/T]aattagctgggcgtg | 4140 |
rs2984138 | snp | G/T | 0 | 0 | intron-variant | MARK3 | GRCh38.p7 | 14:103493511 | TGGCTGGTCATGAAT[G/T]GGTGTCCCAAACCTG | 4140 |
rs2985910 | snp | C/T | | | intron-variant | MARK3 | GRCh38.p7 | 14:103493753 | tgggtagctgggact[C/T]caggcgcccaccacc | 4140 |
rs3071411 | in-del | -/TG | | | intron-variant | MARK3 | GRCh38.p7 | 14:103481652 | GTGTGTGTGTGTGTG[-/TG]TTTCAACATTGTCTT | 4140 |
rs3742458 | snp | A/G | 0.416055 | 0.186885 | intron-variant | MARK3 | GRCh38.p7 | 14:103484031 | GTTGCTAAACCACCT[A/G]CATAGCAGAGACACT | 4140 |
rs3759575 | snp | A/G | 0.45198 | 0.147323 | upstream-variant-2KB | MARK3 | GRCh38.p7 | 14:103384087 | TGGGCGACAGAGCGA[A/G]ACTCCGTCCCAAAAC | 4140 |
rs3759576 | snp | C/T | 0.358515 | 0.225221 | upstream-variant-2KB | MARK3 | GRCh38.p7 | 14:103384096 | GAGCGAAACTCCGTC[C/T]CAAAACAACAACAAC | 4140 |
rs3759577 | snp | C/T | 0.45198 | 0.147323 | upstream-variant-2KB | MARK3 | GRCh38.p7 | 14:103384626 | CTGGCCCGAGGCTGG[C/T]ACCCAGAGATGCTTC | 4140 |
rs3759578 | snp | A/T | | | upstream-variant-2KB | MARK3 | GRCh38.p7 | 14:103384699 | TTATAAACCCCCTAC[A/T]GGCATTTGGAAGCTG | 4140 |
rs3759579 | snp | A/G | 0.486 | 0.0824865 | upstream-variant-2KB | MARK3 | GRCh38.p7 | 14:103384935 | GGTTTGTTGGCGAGA[A/G]CCTGACTCCCGGGTC | 4140 |
rs3759580 | snp | A/G | 0.0023933 | 0.0345097 | upstream-variant-2KB | MARK3 | GRCh38.p7 | 14:103385054 | CCCAGGGATGCAACC[A/G]CAACTTTTGCGCACA | 4140 |
rs3783394 | snp | A/G | 0.331411 | 0.236373 | intron-variant | MARK3 | GRCh38.p7 | 14:103392336 | AGCTTTATGAAACTA[A/G]TCTGTAACTCTCAAA | 4140 |
rs3783395 | snp | C/T | 0.417359 | 0.185718 | intron-variant | MARK3 | GRCh38.p7 | 14:103428683 | TTTTTTTGTACTTTT[C/T]TATTGATATAGTTGT | 4140 |
rs3783396 | snp | A/T | 0.361684 | 0.223667 | intron-variant | MARK3 | GRCh38.p7 | 14:103441504 | TGTTATCCAGGATGG[A/T]CTCGATCTCCTGACC | 4140 |
rs3783397 | snp | A/G | 0.365646 | 0.221644 | intron-variant | MARK3 | GRCh38.p7 | 14:103480952 | GATGGCTGAGTCTAA[A/G]TAGAAACACTGGAGA | 4140 |
rs3783398 | snp | C/T | 0.364609 | 0.222182 | intron-variant | MARK3 | GRCh38.p7 | 14:103483041 | TAAAAGACTGGAAAA[C/T]TATTGGGTTTAACTT | 4140 |
rs3783399 | snp | A/G | 0.496905 | 0.0392151 | intron-variant | MARK3 | GRCh38.p7 | 14:103487980 | GTGAACCCAGGAGGC[A/G]GAGCTTGCAGTGAGC | 4140 |
rs3783400 | snp | A/G | 0.365646 | 0.221644 | intron-variant | MARK3 | GRCh38.p7 | 14:103500708 | GATCAGGGCTTACTC[A/G]AGTTCCCAGGCTTAT | 4140 |
rs3783402 | snp | C/G | 0.419936 | 0.183362 | intron-variant | MARK3 | GRCh38.p7 | 14:103501592 | TGAAATCCCATGGCT[C/G]TTCATAGCTCTCCTC | 4140 |
rs3825566 | snp | C/T | 0.462516 | 0.131669 | intron-variant | MARK3 | GRCh38.p7 | 14:103386388 | AATGGATTGTGCAAA[C/T]GTGTGTGTCAGATCA | 4140 |
rs3837596 | in-del | -/G | 0.378372 | 0.214524 | intron-variant | MARK3 | GRCh38.p7 | 14:103449944 | ATCAAGAATGCATCA[-/G]GCACAAGAATAGAAG | 4140 |
rs3837597 | in-del | -/C | 0.364817 | 0.222075 | intron-variant | MARK3 | GRCh38.p7 | 14:103495793 | ATACTTAATCAGCTA[-/C]TGACAGTTTGTTCTT | 4140 |
rs4143998 | snp | A/G | 0.496583 | 0.0411924 | intron-variant | MARK3 | GRCh38.p7 | 14:103488910 | ATAGCCCCAACATAA[A/G]GCAGATACGTCTTTA | 4140 |
rs4243738 | snp | A/G | 0.48955 | 0.071525 | intron-variant | MARK3 | GRCh38.p7 | 14:103405382 | TTAAGATGGAGTCTC[A/G]CTCTGTCACCCAGGC | 4140 |
rs4243739 | snp | A/G | 0.48955 | 0.071525 | intron-variant | MARK3 | GRCh38.p7 | 14:103405500 | GCAGTACAGGTGCCC[A/G]CCACCACACCCAGCT | 4140 |
rs4900572 | snp | C/T | 0.438105 | 0.164671 | intron-variant | MARK3 | GRCh38.p7 | 14:103402514 | ctgagattgcgccac[C/T]gcactccagctgaca | 4140 |
rs4900573 | snp | C/T | 0.353371 | 0.227628 | intron-variant, upstream-variant-2KB | MARK3 | GRCh38.p7 | 14:103412612 | AAGCCTGACGGTGCC[C/T]GAGAAGCGCTTGTCC | 4140 |
rs4900574 | snp | A/G | 0.417359 | 0.185718 | intron-variant, upstream-variant-2KB | MARK3 | GRCh38.p7 | 14:103412687 | CTTCAGGAACTTGGG[A/G]CACTTTCACTGGTTC | 4140 |
rs4900575 | snp | C/G | 0.361474 | 0.223771 | intron-variant | MARK3 | GRCh38.p7 | 14:103432832 | ctgcattccagcctg[C/G]gcaacagagcaagac | 4140 |
rs4900576 | snp | C/T | 0.0667028 | 0.170006 | intron-variant | MARK3 | GRCh38.p7 | 14:103454934 | ACTCTTTGCTTCTTG[C/T]TTCTTTTATCTCTAA | 4140 |
rs4900577 | snp | A/C | 0.0585053 | 0.160716 | intron-variant | MARK3 | GRCh38.p7 | 14:103458480 | AAAAAAAAAAAGAAG[A/C]AGCAGCTGTAGACAA | 4140 |
rs4900578 | snp | A/T | 0.361894 | 0.223562 | intron-variant | MARK3 | GRCh38.p7 | 14:103459673 | CCCAGCTAATTTTTT[A/T]TTTTTTTTTTTGTAA | 4140 |
rs4900579 | snp | C/T | 0.0700422 | 0.173537 | intron-variant | MARK3 | GRCh38.p7 | 14:103481915 | gggactacaggcgcc[C/T]gccaccactcccagg | 4140 |
rs4900580 | snp | C/T | 0.482008 | 0.0931261 | intron-variant | MARK3 | GRCh38.p7 | 14:103494289 | aggcatggtggctca[C/T]gcctgtaatcccagc | 4140 |
rs4906319 | snp | A/G | 0.496583 | 0.0411924 | intron-variant | MARK3 | GRCh38.p7 | 14:103400983 | TGTGTGTGTGTGTGT[A/G]TGCAGGTTGTTTATT | 4140 |
rs4906320 | snp | C/T | 0.489142 | 0.0728777 | intron-variant | MARK3 | GRCh38.p7 | 14:103410588 | tgcctgtattcatag[C/T]gctttgggaggccaa | 4140 |
rs4906321 | snp | C/T | 0.434543 | 0.168653 | intron-variant, upstream-variant-2KB | MARK3 | GRCh38.p7 | 14:103412545 | GTGGCCTTGGTCTCG[C/T]CACAGTGCTGCTGTT | 4140 |
rs4906322 | snp | A/G | 0.489259 | 0.0724914 | intron-variant, upstream-variant-2KB | MARK3 | GRCh38.p7 | 14:103412695 | ACTTGGGGCACTTTC[A/G]CTGGTTCCCGTGCAG | 4140 |
rs4906323 | snp | A/G | 0.365024 | 0.221967 | intron-variant | MARK3 | GRCh38.p7 | 14:103435631 | GCCAGGATGGTCTCA[A/G]TCTCCTGACCTCATG | 4140 |
rs4906324 | snp | A/G | 0.487495 | 0.0780784 | intron-variant | MARK3 | GRCh38.p7 | 14:103456762 | TTGTTGAATGAATGA[A/G]TATACTCAGGAAATG | 4140 |
rs4906325 | snp | A/G | 0 | 0 | intron-variant | MARK3 | GRCh38.p7 | 14:103458476 | AAAAAAAAAAAAAAA[A/G]AAGCAGCAGCTGTAG | 4140 |
rs4906326 | snp | A/T | 0.0667028 | 0.170006 | intron-variant | MARK3 | GRCh38.p7 | 14:103462320 | TATACTGAGTATTCA[A/T]TATGTGTGAACATTA | 4140 |