SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs8645 | snp | A/C | 0.241914 | 0.249869 | utr-variant-3-prime | SUMO3 | GRCh38.p7 | 21:44806651 | CATTTTTTTAACCCC[A/C]AAATTATAGCCTGAA | 6612 |
rs180313 | snp | C/T | 0.0678174 | 0.1712 | intron-variant | SUMO3 | GRCh38.p7 | 21:44807883 | CTGCTCAGCTGCTCT[C/T]AGCAGCTTCTCCCTG | 6612 |
rs235292 | snp | G/T | 0.106633 | 0.204807 | utr-variant-3-prime | SUMO3 | GRCh38.p7 | 21:44805750 | AGGAAATGAGAACAT[G/T]TCAGCAAGATTTCAA | 6612 |
rs235293 | snp | C/T | 0.0654584 | 0.168655 | intron-variant | SUMO3 | GRCh38.p7 | 21:44809015 | GCACAAATCGGAAGT[C/T]GCCCTGGAACCACGC | 6612 |
rs235334 | snp | A/G | 0.486332 | 0.08153 | intron-variant | SUMO3 | GRCh38.p7 | 21:44815259 | GGGAAGCAAGCATGG[A/G]TGCAGTCCCTGGGTT | 6612 |
rs235335 | snp | C/G | 0.0655868 | 0.168795 | intron-variant | SUMO3 | GRCh38.p7 | 21:44815992 | AGGGGAAGAGGTGGA[C/G]TCTGGGGCCCGGTGG | 6612 |
rs235336 | snp | A/G | 0.0547245 | 0.156101 | intron-variant | SUMO3 | GRCh38.p7 | 21:44816508 | GACCACCCTCCCTTT[A/G]CAGATGAGGGTGGAG | 6612 |
rs235337 | snp | C/T | 0.3742 | 0.216966 | intron-variant | SUMO3 | GRCh38.p7 | 21:44817356 | CACTTCTCCGCATCG[C/T]GTCCCGGCCATCGCG | 6612 |
rs663223 | snp | G/T | 0.0119091 | 0.0762411 | upstream-variant-2KB | SUMO3 | GRCh38.p7 | 21:44818236 | TCCCGCGCGACCCCG[G/T]CGGGCGCGGAAGCCC | 6612 |
rs873301 | snp | C/T | 0.118584 | 0.212673 | intron-variant | SUMO3 | GRCh38.p7 | 21:44808833 | GCCCAGCACTTGGCT[C/T]CATCTCCAAACAGCA | 6612 |
rs1051306 | snp | A/C | | | utr-variant-5-prime | SUMO3 | GRCh38.p7 | 21:44817973 | CCCGCGCCGCTCGCG[A/C]AGCCATGTCCGAGGA | 6612 |
rs1051311 | snp | C/T | 0 | 0 | missense | SUMO3 | GRCh38.p7 | 21:44814014 | ATCAAGAGGCACACG[C/T]CGCTGAGCAAGCTGA | 6612 |
rs1051331 | snp | C/T | 0.285298 | 0.247496 | utr-variant-3-prime | SUMO3 | GRCh38.p7 | 21:44806871 | TGCCGACCACAAAGG[C/T]GTCTGCGGAAACTCG | 6612 |
rs1555002 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | SUMO3 | GRCh38.p7 | 21:44814948 | ACTGGGAGCCAACTT[C/T]GGGGCAGCTCAGTCT | 6612 |
rs1555003 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | SUMO3 | GRCh38.p7 | 21:44814982 | CCGAAAAGTGGGGCA[C/T]CCCTCTGCCGGCCTG | 6612 |
rs2016874 | snp | A/G | 0.0279526 | 0.114869 | intron-variant | SUMO3 | GRCh38.p7 | 21:44809258 | CGGCTTAATTCAAAA[A/G]CCAAATATTTTAATC | 6612 |
rs2017089 | snp | A/G | 0.117886 | 0.21224 | intron-variant | SUMO3 | GRCh38.p7 | 21:44809478 | AACTGCCACTGGTTT[A/G]GCTTTAAGAAGTTCC | 6612 |
rs2329902 | snp | A/G | 0.324382 | 0.238678 | intron-variant | SUMO3 | GRCh38.p7 | 21:44807248 | AGCCCTTACGGTTCA[A/G]CAAGCTTCCCCTAAC | 6612 |
rs2838692 | snp | C/T | 0.23031 | 0.249223 | downstream-variant-500B | SUMO3 | GRCh38.p7 | 21:44805481 | AAATGAGCTGCCAGG[C/T]GAATACTAACCTTCC | 6612 |
rs2838693 | snp | A/C | 0.41441 | 0.188333 | intron-variant | SUMO3 | GRCh38.p7 | 21:44807957 | TTCCTCAAGTAGGTA[A/C]AAATGGATACTTGTT | 6612 |
rs2838694 | snp | C/G | 0.127944 | 0.218179 | intron-variant | SUMO3 | GRCh38.p7 | 21:44810229 | TGAAATGAAGTAAAT[C/G]AAAAAGGCACAAACA | 6612 |
rs2838695 | snp | C/T | 0.320575 | 0.239832 | intron-variant | SUMO3 | GRCh38.p7 | 21:44810837 | CACTGTGCAGCAGCC[C/T]AGAGAGGAGGGGAGG | 6612 |
rs2838696 | snp | C/T | 0.125874 | 0.217008 | intron-variant | SUMO3 | GRCh38.p7 | 21:44813315 | CTGGTGGGCAAAGCC[C/T]ATAAAAGTGGCCTAG | 6612 |
rs2838697 | snp | A/C | 0.325459 | 0.238349 | missense, intron-variant | SUMO3 | GRCh38.p7 | 21:44813921 | TGGGGATGCCTGGAA[A/C]GCACAGGACCAGTGC | 6612 |
rs2838698 | snp | C/T | 0.471958 | 0.115042 | intron-variant | SUMO3 | GRCh38.p7 | 21:44814326 | GTAAAACAATGCAAG[C/T]CTAGGGTCCTCTGAC | 6612 |
rs2838699 | snp | C/T | 0.249038 | 0.249998 | intron-variant | SUMO3 | GRCh38.p7 | 21:44814650 | GTGACTCAGAGGAAC[C/T]CTATGGGACATTCAA | 6612 |
rs2838700 | snp | C/T | 0.471004 | 0.116864 | intron-variant | SUMO3 | GRCh38.p7 | 21:44815998 | GGCCCCAGAGTCCAC[C/T]TCTTCCCCTTCGTCA | 6612 |
rs3746969 | snp | A/G | 1.64776e-05 | 0.00287028 | intron-variant | SUMO3 | GRCh38.p7 | 21:44809121 | TCATTGACAAGCCCT[A/G]GAAAGGAAAAGCAGT | 6612 |
rs3827259 | snp | C/T | 0.067446 | 0.170804 | intron-variant | SUMO3 | GRCh38.p7 | 21:44809509 | CAGTTTCAAAGCAGA[C/T]AGGTAAGTGGTCCAT | 6612 |
rs4437050 | snp | A/C | 0.00345393 | 0.041413 | intron-variant | SUMO3 | GRCh38.p7 | 21:44807059 | TCATGGTTGTCACAA[A/C]AGGCACAGCGAGAGA | 6612 |
rs4818977 | snp | C/T | 0.422944 | 0.180528 | intron-variant | SUMO3 | GRCh38.p7 | 21:44809891 | TGTCCTGGGTCATCC[C/T]TCCCATCTTTCCAGA | 6612 |
rs4818978 | snp | C/T | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44811175 | GCACACACCCACACA[C/T]ACACACACATGCACA | 6612 |
rs7282882 | snp | G/T | 0.418653 | 0.184544 | intron-variant | SUMO3 | GRCh38.p7 | 21:44817494 | CCGAGCCGACTCCGT[G/T]CACTCGACACAGGAT | 6612 |
rs7283053 | snp | A/G/T | 0.0267878 | 0.112589 | intron-variant | SUMO3 | GRCh38.p7 | 21:44817603 | CGGGGACACTGCTGG[A/G/T]GCGGGATCCGAGGGC | 6612 |
rs7283639 | snp | C/T | 0.130694 | 0.219696 | intron-variant | SUMO3 | GRCh38.p7 | 21:44808250 | GGGCGCGTTGGCTCA[C/T]GCCTTTAATCCCAGC | 6612 |
rs9306115 | snp | A/G | 0.422944 | 0.180528 | intron-variant | SUMO3 | GRCh38.p7 | 21:44813156 | AAAATCCACAGGCAA[A/G]AGAGTAAAATAAAAG | 6612 |
rs9306116 | snp | A/T | 0.471958 | 0.115042 | intron-variant | SUMO3 | GRCh38.p7 | 21:44814164 | TAACCGCGACTTGAA[A/T]GGGCAAGTCTTTAGG | 6612 |
rs9306117 | snp | A/C/T | 0.138488 | 0.231878 | intron-variant | SUMO3 | GRCh38.p7 | 21:44816666 | ATGAACACTGGAGAA[A/C/T]GCGACTACAGACCCT | 6612 |
rs9637164 | snp | C/G | | | utr-variant-3-prime | SUMO3 | GRCh38.p7 | 21:44805925 | ACTGAAATCACCAGA[C/G]TAATGCATAAATTCA | 6612 |
rs9637189 | snp | A/G | 0.327445 | 0.237702 | intron-variant | SUMO3 | GRCh38.p7 | 21:44814522 | TCTGGGCAACAGAGC[A/G]AGACCCCATCTCTTT | 6612 |
rs9975507 | snp | A/G | 0.157642 | 0.232314 | intron-variant | SUMO3 | GRCh38.p7 | 21:44812774 | GCCCCCCCCACATGT[A/G]CACGGCCCCACACGC | 6612 |
rs9975777 | snp | C/G | 0.133435 | 0.221162 | intron-variant | SUMO3 | GRCh38.p7 | 21:44816635 | ACACCAAGGGCTTCG[C/G]AAAGGTTCTCTTTTT | 6612 |
rs9976897 | snp | A/G | 0.0520825 | 0.152737 | upstream-variant-2KB | SUMO3 | GRCh38.p7 | 21:44818970 | GCGTCCCTCAGGAGT[A/G]CCCGGGTGGTGCCAG | 6612 |
rs9977439 | snp | A/G | 0.104504 | 0.2033 | intron-variant | SUMO3 | GRCh38.p7 | 21:44813600 | CAGGGTGACAGCGGC[A/G]TGGGGCACACGCCAC | 6612 |
rs9977465 | snp | A/T | 0.422944 | 0.180528 | intron-variant | SUMO3 | GRCh38.p7 | 21:44812352 | cccaaagtgctggga[A/T]tacaggcataagcca | 6612 |
rs9979741 | snp | C/T | 0.135484 | 0.22223 | intron-variant | SUMO3 | GRCh38.p7 | 21:44817151 | ATGGGGAGGAGTGGG[C/T]ACACACCATGGGGGG | 6612 |
rs9981327 | snp | C/T | 0.0513938 | 0.151841 | missense, intron-variant | SUMO3 | GRCh38.p7 | 21:44813951 | CGCACACGGGGAGGC[C/T]CTGCGGGGGAGCAAG | 6612 |
rs9984357 | snp | C/T | 0.362104 | 0.223456 | intron-variant | SUMO3 | GRCh38.p7 | 21:44807688 | CAGCAAGGCTGGAAG[C/T]AGTCATGCTCCCAGA | 6612 |
rs10483079 | snp | C/G | 0.0252325 | 0.109451 | utr-variant-3-prime | SUMO3 | GRCh38.p7 | 21:44806623 | AGATCCCTGGCCAGA[C/G]TAAAAGCGAACATTC | 6612 |
rs10658457 | snp | C/T | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44812053 | cactgaacttctcac[C/T]ttttttttttttttt | 6612 |
rs11545089 | snp | C/G | 0.00597247 | 0.0543191 | utr-variant-3-prime | SUMO3 | GRCh38.p7 | 21:44806362 | GGTTAAAAAATAACC[C/G]AGTCTTTTGGTAATT | 6612 |
rs11545091 | snp | C/G | | | utr-variant-5-prime | SUMO3 | GRCh38.p7 | 21:44818002 | GCTCCGCGCTGCTTC[C/G]CCCGCGCCGCCTCCC | 6612 |
rs11545092 | snp | A/G/T | 9.92185e-05 | 0.00704276 | synonymous-codon | SUMO3 | GRCh38.p7 | 21:44814012 | CAAGAGGCACACGCC[A/G/T]CTGAGCAAGCTGATG | 6612 |
rs11701732 | snp | C/T | 0.426354 | 0.177198 | upstream-variant-2KB | SUMO3 | GRCh38.p7 | 21:44819512 | TCGACTCCAAGACAC[C/T]GTTAATCATAAAACA | 6612 |
rs11702064 | snp | C/T | 0.248755 | 0.249997 | intron-variant | SUMO3 | GRCh38.p7 | 21:44815048 | TGAGGCAGGGCCCTC[C/T]GGCTCACTCTGAAAG | 6612 |
rs11911014 | snp | C/T | 0.0970103 | 0.197722 | intron-variant | SUMO3 | GRCh38.p7 | 21:44814968 | CAGCTCAGTCTGAGC[C/T]GAAAAGTGGGGCACC | 6612 |
rs13046717 | snp | C/T | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44810993 | acacccatgcacaca[C/T]ccacacaTGcacaca | 6612 |
rs13046718 | snp | A/C | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44810994 | CACCCATGCACACAC[A/C]CACACATGCACACAC | 6612 |
rs13049657 | snp | A/G | 0.248471 | 0.249995 | intron-variant | SUMO3 | GRCh38.p7 | 21:44811835 | ggaacagagtctgga[A/G]aaggatacaaattat | 6612 |
rs13050872 | snp | C/G | 0.367922 | 0.220441 | missense, intron-variant | SUMO3 | GRCh38.p7 | 21:44813948 | GTGCGCACACGGGGA[C/G]GCTCTGCGGGGGAGC | 6612 |
rs17217834 | snp | A/G | 0.117537 | 0.212022 | intron-variant | SUMO3 | GRCh38.p7 | 21:44813057 | AGGGGCTGCTTGCCA[A/G]TAAAGAATGCAAGGC | 6612 |
rs17526563 | snp | C/T | 0.127944 | 0.218179 | upstream-variant-2KB | SUMO3 | GRCh38.p7 | 21:44818544 | GGCGGGTGGCGCCCC[C/T]AATCGTCTAGGGTGC | 6612 |
rs17526570 | snp | C/G | | | upstream-variant-2KB | SUMO3 | GRCh38.p7 | 21:44818207 | GACCCGCCCCGTGAC[C/G]CATCTCCAACCGCCC | 6612 |
rs35209448 | in-del | -/CA | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44813395 | ACAGACACACACACA[-/CA]CCACGTCACAAACAG | 6612 |
rs35934209 | snp | A/G | 0.0966517 | 0.197444 | intron-variant | SUMO3 | GRCh38.p7 | 21:44815397 | AAGGTGCGTGTCCTG[A/G]GGCGGCACTCACCCC | 6612 |
rs56230948 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SUMO3 | GRCh38.p7 | 21:44811708 | TTGAAATGACCTCCC[A/G]GAAAGAAGCCCAAAT | 6612 |
rs56656758 | snp | C/T | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44808072 | ACATTCCAGTGGATT[C/T]TCACAACATTGAAAG | 6612 |
rs57205597 | snp | A/G | 0.133435 | 0.221162 | intron-variant | SUMO3 | GRCh38.p7 | 21:44816760 | GAGGCACACCCCAGC[A/G]TGGCAATGGGGGAGA | 6612 |
rs57451321 | snp | C/G | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44808367 | AATACAAAAAAATTA[C/G]CCGGGAGTGGTGGTG | 6612 |
rs59498244 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | SUMO3 | GRCh38.p7 | 21:44807963 | AAGTAGGTACAAATG[A/G]ATACTTGTTGCAAAG | 6612 |
rs59528804 | in-del | -/CCACATATGCACACAC | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44811010 | CACACATGCACACAC[-/CCACATATGCACACAC]GCACACACCCACATA | 6612 |
rs59575993 | in-del | -/AT | 0.426047 | 0.177503 | intron-variant | SUMO3 | GRCh38.p7 | 21:44810497 | CCCACGGCAGCACAC[-/AT]GAGATGTGCTTTCTG | 6612 |
rs59687051 | snp | C/G | 0.0785177 | 0.181917 | upstream-variant-2KB | SUMO3 | GRCh38.p7 | 21:44819563 | GACACACTAAACTCC[C/G]GCAGGCTGTGGATGA | 6612 |
rs59713448 | in-del | -/TGGACACCAGGA | 0 | 0 | intron-variant | SUMO3 | GRCh38.p7 | 21:44815801 | TCTGCTCCAAACAGA[-/TGGACACCAGGA]ATGACGATCTGTCCC | 6612 |
rs60007138 | snp | C/G | 0.0115144 | 0.0749975 | intron-variant | SUMO3 | GRCh38.p7 | 21:44816455 | ACCATGGTTCCTGAC[C/G]GTTCCATCCCACTTC | 6612 |
rs60685574 | snp | G/T | 0.141934 | 0.225437 | intron-variant | SUMO3 | GRCh38.p7 | 21:44811159 | ACACATACACACACA[G/T]GCACACACCCACACA | 6612 |
rs61602523 | snp | G/T | 0.146314 | 0.227484 | upstream-variant-2KB | SUMO3 | GRCh38.p7 | 21:44819532 | ATCATAAAACAACAC[G/T]ACCGTAGGTAGCACA | 6612 |
rs62220110 | snp | A/G | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44809990 | AGGTTGTGTGCCAAT[A/G]AGGGACAGATAAGAA | 6612 |
rs67264081 | in-del | -/GATGGACACCAG | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44815800 | CTCTGCTCCAAACAG[-/GATGGACACCAG]AATGACGATCTGTCC | 6612 |
rs67879920 | in-del | -/GAGGACAGGGTGACAGCGGCG | 0.355096 | 0.226837 | intron-variant | SUMO3 | GRCh38.p7 | 21:44813580 | GGCCAGCTCATACGC[-/GAGGACAGGGTGACAGCGGCG]TGGGGCACACGCCAC | 6612 |
rs71199631 | in-del | -/AC | 0.35445 | 0.227135 | intron-variant | SUMO3 | GRCh38.p7 | 21:44813384 | TACCAAGAACAACAG[-/AC]ACACACACACACCAC | 6612 |
rs71199633 | in-del | -/G | 0 | 0 | intron-variant | SUMO3 | GRCh38.p7 | 21:44815711 | ACGTCCCCCACAGGG[-/G]TAATGGCTGCAGCCC | 6612 |
rs71322592 | snp | C/G | 0.248188 | 0.249993 | intron-variant | SUMO3 | GRCh38.p7 | 21:44817206 | ACCGGGGGGCGCGAT[C/G]GGGAGGGGTGGGCGC | 6612 |
rs72613649 | snp | A/G | 0.424348 | 0.179172 | intron-variant | SUMO3 | GRCh38.p7 | 21:44817645 | CAGGAGCAGCAGCGC[A/G]GGGCCCGACACCGGG | 6612 |
rs73232962 | snp | A/G | 0.106278 | 0.204558 | intron-variant | SUMO3 | GRCh38.p7 | 21:44807449 | TTTATACCAAGTGCG[A/G]GGGACCATGCCATGA | 6612 |
rs73232964 | snp | C/T | 0.5 | 0 | intron-variant | SUMO3 | GRCh38.p7 | 21:44812054 | ACTGAACTTCTCACC[C/T]TTTTTTTTTTTTTTT | 6612 |
rs73232966 | snp | C/T | 0.127599 | 0.217986 | upstream-variant-2KB | SUMO3 | GRCh38.p7 | 21:44819390 | CAGCTCAGACGGTCC[C/T]GGGAGGGGGCTCCGC | 6612 |
rs73372511 | snp | C/T | 0.148661 | 0.22854 | intron-variant | SUMO3 | GRCh38.p7 | 21:44811495 | GAGGATCACTTGAGC[C/T]CCAGGGCTCAAGGCT | 6612 |
rs73372522 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | SUMO3 | GRCh38.p7 | 21:44815659 | TCTTTAGGGAAGGAA[C/G]GTATGAGTGTGTTCA | 6612 |
rs73906926 | snp | A/G | 0.0119091 | 0.0762411 | upstream-variant-2KB | SUMO3 | GRCh38.p7 | 21:44820013 | GGGTAAAGAACCCAA[A/G]TGGCCAGAGCCCCTC | 6612 |
rs74706647 | snp | A/G | 0.0437281 | 0.141251 | intron-variant | SUMO3 | GRCh38.p7 | 21:44809412 | ATCTTCTCTCTGATG[A/G]GCTAAAACGGCTCAT | 6612 |
rs74881430 | snp | A/C | 0.0130921 | 0.0798413 | intron-variant | SUMO3 | GRCh38.p7 | 21:44809263 | TAATTCAAAAACCAA[A/C]TATTTTAATCCAAGT | 6612 |
rs75760356 | snp | C/G | 0.5 | 0 | intron-variant | SUMO3 | GRCh38.p7 | 21:44807793 | CAGGCAGGGCTCCCT[C/G]TGCCTCTCGGTCCAC | 6612 |
rs76003441 | snp | G/T | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44808722 | CCAGCTGGCCCCTAA[G/T]CTGCACACGGGCTAC | 6612 |
rs76299308 | snp | C/G | 0.130351 | 0.219509 | intron-variant | SUMO3 | GRCh38.p7 | 21:44815493 | TGAGTGGTGAGCTGG[C/G]ACACCCCCATCTCCC | 6612 |
rs76430289 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | SUMO3 | GRCh38.p7 | 21:44811768 | GAAAAATTATCAAAT[G/T]TAAAATATCTAGGAC | 6612 |
rs76455805 | snp | C/T | 0.130351 | 0.219509 | downstream-variant-500B | SUMO3, LINC01424 | GRCh38.p7 | 21:44805152 | GGTTTTGTTACACCA[C/T]TGCACACTGGGAAAT | 6612 |
rs76559724 | in-del | -/CGAGGACAGGGTGACAGCGGCG | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44813579 | AGGCCAGCTCATACG[-/CGAGGACAGGGTGACAGCGGCG]TGGGGCACACGCCAC | 6612 |
rs76675574 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | SUMO3 | GRCh38.p7 | 21:44815005 | CCGGCCTGCACTGCT[A/G]GGATAAAGTCGTTTG | 6612 |
rs77015779 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | SUMO3 | GRCh38.p7 | 21:44815499 | GTGAGCTGGCACACC[C/T]CCATCTCCCCATCCC | 6612 |
rs77279225 | snp | C/T | 0.0115144 | 0.0749975 | upstream-variant-2KB | SUMO3 | GRCh38.p7 | 21:44819212 | CTACTCAAAAATTCA[C/T]TTTCTTGGCTAGAGC | 6612 |
rs77748262 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | SUMO3 | GRCh38.p7 | 21:44816302 | TAAATATTCAAACAA[A/C]CCCAGAGTGGGAGAA | 6612 |
rs77760544 | snp | C/T | 0.5 | 0 | intron-variant | SUMO3 | GRCh38.p7 | 21:44814482 | GACGTGGGAGGATGG[C/T]GTAAGCCCAGGAGTT | 6612 |
rs78208377 | snp | C/T | 0.122064 | 0.214785 | intron-variant | SUMO3 | GRCh38.p7 | 21:44810472 | GCAGGACCCCCACAA[C/T]CCTGTGCCTCCCACG | 6612 |
rs78595373 | snp | A/G/T | 0.00716521 | 0.0594565 | downstream-variant-500B | SUMO3 | GRCh38.p7 | 21:44805500 | TACTAACCTTCCAGC[A/G/T]GCTAGCTTTTCAATC | 6612 |
rs78777134 | snp | A/G | 0.116488 | 0.211364 | intron-variant | SUMO3 | GRCh38.p7 | 21:44815415 | CGGCACTCACCCCCC[A/G]ACTCCAGTCTTGGGC | 6612 |
rs78836286 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | SUMO3 | GRCh38.p7 | 21:44809945 | CTGGCACCACTACTT[C/G/T]CCCCCTTTACAAAGT | 6612 |
rs79119995 | snp | C/G | 0.084364 | 0.187256 | downstream-variant-500B | SUMO3 | GRCh38.p7 | 21:44805397 | TCAGCCAGGAGGTCT[C/G]TGAGGAGAGGATGCA | 6612 |
rs79772434 | snp | A/G | 0.000742691 | 0.019256 | synonymous-codon | SUMO3 | GRCh38.p7 | 21:44814048 | GAACTGCACCACGGA[A/G]CCGTCCTGCCCGGCC | 6612 |
rs80015658 | snp | A/C/G | 0.0103295 | 0.0711199 | intron-variant | SUMO3 | GRCh38.p7 | 21:44807426 | TAGGACCCACAGGAG[A/C/G]CTTGCGCTTTATACC | 6612 |
rs111414442 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | SUMO3 | GRCh38.p7 | 21:44810172 | CTGAAACAGGACAGA[C/G/T]GGGGTTAAAACGTGC | 6612 |
rs111602253 | snp | A/G | | | upstream-variant-2KB | SUMO3 | GRCh38.p7 | 21:44818229 | GGGCGGGTCCCGCGC[A/G]ACCCCGTCGGGCGCG | 6612 |
rs111608199 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | SUMO3 | GRCh38.p7 | 21:44813489 | GGAAGAAGGGGAAAG[A/C]ATCACGCGCTTTCTT | 6612 |
rs111656051 | in-del | -/C | 0.5 | 0 | intron-variant | SUMO3 | GRCh38.p7 | 21:44812760 | GGGGGAAGGGCAGAG[-/C]CCCCCCCACATGTAC | 6612 |
rs111778283 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SUMO3 | GRCh38.p7 | 21:44809304 | TGATATGCAGATTTA[G/T]GATCCAGCTCAGTAT | 6612 |
rs111882639 | snp | A/G | 0.5 | 0 | intron-variant | SUMO3 | GRCh38.p7 | 21:44808991 | CGTATCCCAAATGGC[A/G]GTTACCCCGCACAAA | 6612 |
rs111959345 | snp | C/G/T | 0 | 0 | utr-variant-3-prime | SUMO3 | GRCh38.p7 | 21:44806630 | TGGCCAGACTAAAAG[C/G/T]GAACATTCAGGCTAT | 6612 |
rs112016907 | in-del | -/A | 0.5 | 0 | intron-variant | SUMO3 | GRCh38.p7 | 21:44812438 | TCTGAAATAAAAAAG[-/A]AAAAAAAGTTTCAAC | 6612 |
rs112536684 | snp | A/C/G | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44816916 | GATGGGGAGGGGTGG[A/C/G]CGCACATCGTGGAGG | 6612 |
rs112869378 | snp | C/T | 0.5 | 0 | intron-variant | SUMO3 | GRCh38.p7 | 21:44811001 | GCACACACCCACACA[C/T]GCACACACCCACATA | 6612 |
rs112870818 | snp | A/G | 0.00659097 | 0.0570267 | missense | SUMO3 | GRCh38.p7 | 21:44806982 | GCCAGGCTGCTCTCC[A/G]GCACACCTCCCGTCT | 6612 |
rs112907174 | snp | C/T | 0.5 | 0 | intron-variant | SUMO3 | GRCh38.p7 | 21:44812465 | CAACCGAGAATATTA[C/T]GTGCAGCCACATACT | 6612 |
rs113070286 | snp | A/G | 0.5 | 0 | intron-variant | SUMO3 | GRCh38.p7 | 21:44808672 | ATTCTGCCCACCCAC[A/G]TCACTTGTGCAAGAT | 6612 |
rs113212756 | snp | G/T | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44816881 | GATAGGGAGGGGTGG[G/T]CACACACTATAGGGG | 6612 |
rs113379284 | snp | A/C/G | 0.00636936 | 0.0560724 | utr-variant-3-prime | SUMO3 | GRCh38.p7 | 21:44806546 | CTGCATCCCCACTGC[A/C/G]GGAAACACCAATTCT | 6612 |
rs113383188 | snp | C/T | 0.0236746 | 0.106192 | utr-variant-3-prime | SUMO3 | GRCh38.p7 | 21:44806545 | GCTGCATCCCCACTG[C/T]GGGAAACACCAATTC | 6612 |
rs113467905 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | SUMO3 | GRCh38.p7 | 21:44813011 | AGGTGAAAATAAGAT[C/T]TGCCCTCAGCAAACA | 6612 |
rs113680780 | snp | A/C | 0.5 | 0 | intron-variant | SUMO3 | GRCh38.p7 | 21:44807101 | GTTAGTTTTCATCAG[A/C]GAGTGGGAAGATCCT | 6612 |
rs113862424 | snp | A/C | 0.00993419 | 0.0697739 | intron-variant | SUMO3 | GRCh38.p7 | 21:44813431 | AGAAGGCATCCACCC[A/C]GCTGGGCACTGCCAG | 6612 |
rs114258888 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | SUMO3 | GRCh38.p7 | 21:44815411 | GGGGCGGCACTCACC[C/T]CCCGACTCCAGTCTT | 6612 |
rs114266294 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | SUMO3 | GRCh38.p7 | 21:44814213 | AGTCATCAAAACCAA[C/T]CTAATTCTTAAAATT | 6612 |
rs114523049 | snp | A/G | 0.0232847 | 0.105357 | intron-variant | SUMO3 | GRCh38.p7 | 21:44816911 | GGCGTGATGGGGAGG[A/G]GTGGGCGCACATCGT | 6612 |
rs114655158 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | SUMO3 | GRCh38.p7 | 21:44811440 | AGCCAGGCGTGGTGG[C/T]GTGTACCTGGAGTCC | 6612 |
rs114697535 | snp | A/G | 0.0168055 | 0.0901129 | intron-variant | SUMO3 | GRCh38.p7 | 21:44813000 | TCACCTTTCGCAGGT[A/G]AAAATAAGATCTGCC | 6612 |
rs114879969 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | SUMO3 | GRCh38.p7 | 21:44815928 | CCTCAGCTATCCAGG[A/G]AAGTCAGAACCATTC | 6612 |
rs114887802 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | SUMO3 | GRCh38.p7 | 21:44813178 | AAATAAAAGGGCAAC[A/G]AGTTGCTGTATTTTC | 6612 |
rs115077807 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | SUMO3 | GRCh38.p7 | 21:44816941 | TGGAGGGGGTGATGG[A/G]GAGGGGTGGACGCAC | 6612 |
rs115235499 | snp | C/T | 0.029116 | 0.117091 | intron-variant | SUMO3 | GRCh38.p7 | 21:44811432 | AAAAAATGAGCCAGG[C/T]GTGGTGGCGTGTACC | 6612 |
rs115489308 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | SUMO3 | GRCh38.p7 | 21:44812804 | CCTGCCATCCCGCAG[C/T]GCAGAGGAGAACATG | 6612 |
rs116059808 | snp | C/T | 0.00564915 | 0.0528456 | missense, intron-variant | SUMO3 | GRCh38.p7 | 21:44813936 | CGCACAGGACCAGTG[C/T]GCACACGGGGAGGCT | 6612 |
rs116062579 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SUMO3 | GRCh38.p7 | 21:44812967 | AAGACCGGGACCTGC[A/G]TGTCTGGAAGCTCAG | 6612 |
rs116147368 | snp | A/C/G | 0.0107386 | 0.0726288 | intron-variant | SUMO3 | GRCh38.p7 | 21:44810810 | CTGCGTGAGAGCAGT[A/C/G]AGGGAAAGGCTCACT | 6612 |
rs116249423 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | SUMO3 | GRCh38.p7 | 21:44812228 | CACCTGGCTAATTTT[C/T]TTAATGTTTCGTAGA | 6612 |
rs116405227 | snp | A/C | 0.0966517 | 0.197444 | upstream-variant-2KB | SUMO3 | GRCh38.p7 | 21:44818567 | CACCCGCCTCCCTGC[A/C]GCCGCGGTTTCCTGT | 6612 |
rs116454398 | snp | A/G | 0.0236746 | 0.106192 | intron-variant | SUMO3 | GRCh38.p7 | 21:44810262 | AAGGACAAAGAAAAC[A/G]GGAGTGGGGATGGGC | 6612 |
rs116964911 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | SUMO3 | GRCh38.p7 | 21:44811386 | CCAGACCAGCCTGGA[A/C]CACATAAGGAGACCC | 6612 |
rs117165413 | snp | A/G | 0.00676609 | 0.0577691 | upstream-variant-2KB | SUMO3 | GRCh38.p7 | 21:44820110 | ATGAGTAACAGCATT[A/G]CTGACATGAAAGCTC | 6612 |
rs117703785 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SUMO3 | GRCh38.p7 | 21:44809420 | TCTGATGAGCTAAAA[C/T]GGCTCATTTTCAACC | 6612 |
rs117721463 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | SUMO3 | GRCh38.p7 | 21:44813006 | TTCGCAGGTGAAAAT[A/C]AGATCTGCCCTCAGC | 6612 |
rs117843275 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | SUMO3 | GRCh38.p7 | 21:44809426 | GAGCTAAAACGGCTC[A/G]TTTTCAACCCAGGTT | 6612 |
rs118156675 | snp | A/G | 0.0471566 | 0.146132 | intron-variant | SUMO3 | GRCh38.p7 | 21:44808613 | TGTCTGCATGTGCCT[A/G]AGAGAAACGAGCTGT | 6612 |
rs138039294 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SUMO3 | GRCh38.p7 | 21:44808671 | CATTCTGCCCACCCA[C/T]GTCACTTGTGCAAGA | 6612 |
rs138078875 | snp | A/G | | | utr-variant-3-prime | SUMO3 | GRCh38.p7 | 21:44806044 | GTAGCTCTTATACAC[A/G]ACAACATAACTGCAA | 6612 |
rs138124467 | snp | A/G | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44810249 | AGGCACAAACAGGAA[A/G]GACAAAGAAAACGGG | 6612 |
rs138153344 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SUMO3 | GRCh38.p7 | 21:44813059 | GGGCTGCTTGCCAAT[A/G]AAGAATGCAAGGCAG | 6612 |
rs138575148 | snp | C/G | 0.00914312 | 0.0669923 | intron-variant | SUMO3 | GRCh38.p7 | 21:44812808 | CCATCCCGCAGCGCA[C/G]AGGAGAACATGGGCA | 6612 |
rs138672270 | snp | G/T | 0.00874735 | 0.0655527 | utr-variant-3-prime | SUMO3 | GRCh38.p7 | 21:44806676 | AAAATGTTGTAGGAG[G/T]GGGGGAAAACACAAA | 6612 |
rs138818295 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | SUMO3 | GRCh38.p7 | 21:44813259 | TCCCTGGGGAAGGGC[A/G]CCTGGCTGCAGGGCC | 6612 |
rs139936877 | in-del | -/TG | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44811017 | GCACACACCCACATA[-/TG]CACACACGCACACAC | 6612 |
rs140102653 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SUMO3 | GRCh38.p7 | 21:44810700 | GCAATCCAGACAGAT[A/C]ACCCCATGTGGATGC | 6612 |
rs140122156 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SUMO3 | GRCh38.p7 | 21:44807312 | TTAACTGAGAGAAAA[A/G]CTGAGTCTAGAAGAT | 6612 |
rs140275998 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SUMO3 | GRCh38.p7 | 21:44814938 | ATGTCAAGAGACTGG[A/G]AGCCAACTTCGGGGC | 6612 |
rs140922461 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | SUMO3 | GRCh38.p7 | 21:44818686 | GTGAAGAAACTGAGG[C/T]ACTGGGAGGTCAAAC | 6612 |
rs141025475 | snp | C/T | 0.0170251 | 0.090679 | upstream-variant-2KB | SUMO3 | GRCh38.p7 | 21:44820037 | GCCCCTCCGGAGGGT[C/T]GCCACACCTGGCGAT | 6612 |
rs141060298 | snp | A/G | 0.00259814 | 0.0359489 | synonymous-codon, intron-variant | SUMO3 | GRCh38.p7 | 21:44813937 | GCACAGGACCAGTGC[A/G]CACACGGGGAGGCTC | 6612 |
rs141072860 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | SUMO3 | GRCh38.p7 | 21:44815195 | GGGACAACTGTCCCA[A/G]CGATGCCTAAATACA | 6612 |
rs141098602 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | SUMO3 | GRCh38.p7 | 21:44811850 | GAAGGATACAAATTA[C/T]CAGAGAACTAACATA | 6612 |
rs141141907 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | SUMO3 | GRCh38.p7 | 21:44808328 | CCATCCTGGCTAACA[C/T]GGTGAAACCCCGTCT | 6612 |
rs141195217 | in-del | -/GAG | 0.117537 | 0.212022 | intron-variant | SUMO3 | GRCh38.p7 | 21:44810859 | GAGGGGAGGAGCGCA[-/GAG]GAGAACGGACAGGAA | 6612 |
rs141301031 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SUMO3 | GRCh38.p7 | 21:44809988 | ACAGGTTGTGTGCCA[A/C]TGAGGGACAGATAAG | 6612 |
rs142010741 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SUMO3 | GRCh38.p7 | 21:44813368 | TGAGTCCGCCACAGC[A/G]TTACCAAGAACAACA | 6612 |
rs142017942 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | SUMO3 | GRCh38.p7 | 21:44812700 | GAGCAGCCAGCCTCA[A/C]AAGCAGCAGTGCAGG | 6612 |
rs142097939 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SUMO3 | GRCh38.p7 | 21:44814766 | TGTGAGGGAAGCCAC[C/T]TCCGAGTACTTTCTG | 6612 |
rs142164138 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | SUMO3 | GRCh38.p7 | 21:44808834 | CCCAGCACTTGGCTC[C/T]ATCTCCAAACAGCAA | 6612 |
rs142525236 | in-del | -/C | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44812051 | CCACTGAACTTCTCA[-/C]CCTTTTTTTTTTTTT | 6612 |
rs142568487 | snp | G/T | 0.0146672 | 0.084371 | upstream-variant-2KB | SUMO3 | GRCh38.p7 | 21:44819864 | ATGCAAAAAGGCTCT[G/T]TCGCAGCTGTGGGGA | 6612 |
rs142762786 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SUMO3 | GRCh38.p7 | 21:44813082 | CAAGGCAGTCGCCAG[A/T]GACTGCCCCTATGAG | 6612 |
rs142956634 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | SUMO3 | GRCh38.p7 | 21:44811493 | GGGAGGATCACTTGA[C/G]CCCCAGGGCTCAAGG | 6612 |
rs143354761 | in-del | -/TGCACAC | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44817251 | GATGGAGGCGGTGGG[-/TGCACAC]GGGGCGCGATGGGTG | 6612 |
rs143596085 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | SUMO3 | GRCh38.p7 | 21:44812958 | TCTGCTGGGAAGACC[A/G]GGACCTGCGTGTCTG | 6612 |
rs143632218 | in-del | -/A | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44813737 | CGCCCTGTCAGGAAG[-/A]AAAACCCACCACACT | 6612 |
rs143788750 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SUMO3 | GRCh38.p7 | 21:44810824 | TCAGGGAAAGGCTCA[C/T]TGTGCAGCAGCCTAG | 6612 |
rs143802170 | snp | C/T | 0.000116299 | 0.00762471 | synonymous-codon | SUMO3 | GRCh38.p7 | 21:44806981 | TGCCAGGCTGCTCTC[C/T]GGCACACCTCCCGTC | 6612 |
rs144060064 | snp | A/G | 9.90557e-05 | 0.0070369 | synonymous-codon | SUMO3 | GRCh38.p7 | 21:44814051 | CTGCACCACGGAGCC[A/G]TCCTGCCCGGCCACC | 6612 |
rs144266028 | snp | C/T | 5.06222e-05 | 0.00503076 | intron-variant | SUMO3 | GRCh38.p7 | 21:44807068 | TCACAACAGGCACAG[C/T]GAGAGAGAGGGGAGC | 6612 |
rs144658156 | snp | C/T | 0.00148388 | 0.0271981 | utr-variant-3-prime | SUMO3 | GRCh38.p7 | 21:44806932 | CGAGGATGGACGGCC[C/T]GGGCTGGGGACGGGC | 6612 |
rs144809126 | in-del | -/GATGGACACCAG | 0.321292 | 0.23962 | intron-variant | SUMO3 | GRCh38.p7 | 21:44815799 | CCTCTGCTCCAAACA[-/GATGGACACCAG]GAATGACGATCTGTC | 6612 |
rs144905450 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SUMO3 | GRCh38.p7 | 21:44815303 | CTGGGGAGACCCTGG[A/G]GAGGCATGGTGCTCT | 6612 |
rs145445571 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SUMO3 | GRCh38.p7 | 21:44808164 | AGTGATGCTTGGTCA[C/T]GGGGCCATCAGCTGA | 6612 |
rs145511543 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | SUMO3 | GRCh38.p7 | 21:44819580 | CAGGCTGTGGATGAC[A/G]GCAGCCCGCTTCAGT | 6612 |
rs145783468 | in-del | -/AC/CA | | | | | GRCh38.p7 | 21:44813386 | CCAAGAACAACAGAC[-/AC/CA]ACACACACACCACGT | 6612 |
rs146085457 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | SUMO3 | GRCh38.p7 | 21:44810631 | TCCAGGAGGCTGGCC[A/G]GAGCCTGGAGGACTC | 6612 |
rs146097096 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant | SUMO3 | GRCh38.p7 | 21:44807181 | TGGCTCTTGTCCGTC[C/G]CCTCACTGCAGCTCA | 6612 |
rs146445149 | snp | A/G | 0.000676517 | 0.0183794 | synonymous-codon | SUMO3 | GRCh38.p7 | 21:44814060 | GGAGCCGTCCTGCCC[A/G]GCCACCTTCAGGTTG | 6612 |
rs146461062 | in-del | -/G | 0.02016 | 0.0983543 | intron-variant | SUMO3 | GRCh38.p7 | 21:44810432 | TCTGAACAGCTGCCT[-/G]GAAGTTCACATGCAG | 6612 |
rs146562340 | snp | A/G | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44813581 | GCCAGCTCATACGCG[A/G]GGACAGGGTGACAGC | 6612 |
rs146790298 | in-del | -/GCACACACCCACATATGCACACAC | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44811002 | CACACACCCACACAT[-/GCACACACCCACATATGCACACAC]GCACACACCCACATA | 6612 |
rs146952863 | snp | A/G | 0.0460573 | 0.144594 | intron-variant | SUMO3 | GRCh38.p7 | 21:44808370 | ACAAAAAAATTAGCC[A/G]GGAGTGGTGGTGGGC | 6612 |
rs146962847 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | SUMO3 | GRCh38.p7 | 21:44805770 | CAAGATTTCAAGCAA[G/T]CAAGAGATGATGGGT | 6612 |
rs147541091 | snp | C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | SUMO3 | GRCh38.p7 | 21:44818975 | CCTCAGGAGTGCCCG[C/G]GTGGTGCCAGCCGGG | 6612 |
rs147549284 | snp | C/T | 0.0120506 | 0.0766818 | missense, intron-variant | SUMO3 | GRCh38.p7 | 21:44813953 | CACACGGGGAGGCTC[C/T]GCGGGGGAGCAAGGT | 6612 |
rs148093505 | in-del | -/TGGACACCAGGA | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44815790 | GCCACAGTGCCTCTG[-/TGGACACCAGGA]CTCCAAACAGAATGA | 6612 |
rs148125507 | snp | A/C | 0.0524604 | 0.153226 | intron-variant | SUMO3 | GRCh38.p7 | 21:44816863 | GCGCACACCGTGGGG[A/C]GTGATAGGGAGGGGT | 6612 |
rs148248359 | snp | C/G/T | 0.0178334 | 0.0929179 | intron-variant | SUMO3 | GRCh38.p7 | 21:44809759 | GGAGGGGAAATGAGC[C/G/T]GCCAGGTGAATACTA | 6612 |
rs148440304 | snp | G/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | SUMO3 | GRCh38.p7 | 21:44819670 | ACCGCTCGAAATTAC[G/T]CCAGTTGCTGTGTCA | 6612 |
rs148509510 | snp | A/C/G | 0.0151836 | 0.0857989 | utr-variant-3-prime | SUMO3 | GRCh38.p7 | 21:44806934 | AGGATGGACGGCCCG[A/C/G]GCTGGGGACGGGCCC | 6612 |
rs148679100 | snp | A/G/T | 0.000214189 | 0.0103466 | missense, synonymous-codon | SUMO3 | GRCh38.p7 | 21:44809086 | GATTGGCTGCCCGTC[A/G/T]AACCTGAATCTGATC | 6612 |
rs148881367 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | SUMO3 | GRCh38.p7 | 21:44812921 | CTGGATCACGGGGCC[C/T]ACACGGCGCCAGGCC | 6612 |
rs149238021 | snp | G/T | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44813580 | GGCCAGCTCATACGC[G/T]AGGACAGGGTGACAG | 6612 |
rs149347205 | snp | A/G | 0.000834893 | 0.0204144 | utr-variant-3-prime | SUMO3 | GRCh38.p7 | 21:44806865 | TGTCCTCGAGTTTCC[A/G]CAGACACCTTTGTGG | 6612 |
rs149359428 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | SUMO3 | GRCh38.p7 | 21:44815626 | CTTCACTTCCCCAAG[C/G]ATGAGGATGCACTGG | 6612 |
rs149621736 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | SUMO3 | GRCh38.p7 | 21:44813517 | CTTGCCTTTCCTAAC[A/G]AAATGGAAAACCACA | 6612 |
rs149674532 | snp | C/G | 0.00636936 | 0.0560724 | upstream-variant-2KB | SUMO3 | GRCh38.p7 | 21:44819326 | TGTGGTCCCTTCCTT[C/G]TGGAACCTGGAGCCC | 6612 |
rs150488974 | in-del | -/CACACATA | 0.117886 | 0.21224 | intron-variant | SUMO3 | GRCh38.p7 | 21:44811169 | ACACAGGCACACACC[-/CACACATA]CACACACATGCACAA | 6612 |
rs150782487 | snp | C/T | 0.000132192 | 0.00812887 | synonymous-codon | SUMO3 | GRCh38.p7 | 21:44814021 | GCTCAGCGGCGTGTG[C/T]CTCTTGATCTTGAAC | 6612 |
rs150804515 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SUMO3 | GRCh38.p7 | 21:44810045 | TACCACCATGACTTT[C/G]GCCTTGAGGAGGGCA | 6612 |
rs151125447 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | SUMO3 | GRCh38.p7 | 21:44811685 | CCACAGGAAGTGGAA[A/G]GATAAAGTTGAAATG | 6612 |
rs151178898 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SUMO3 | GRCh38.p7 | 21:44814873 | CAACAATGGCACAAT[C/T]GGGGTGTCTTGTTGC | 6612 |
rs151325504 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SUMO3 | GRCh38.p7 | 21:44807602 | CCTGACACAGTGGGC[A/G]CAAAACACCCACCCT | 6612 |
rs180744693 | snp | C/T | 0.00835141 | 0.0640778 | upstream-variant-2KB | SUMO3 | GRCh38.p7 | 21:44820111 | TGAGTAACAGCATTG[C/T]TGACATGAAAGCTCG | 6612 |
rs180857289 | snp | A/G | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44814483 | ACGTGGGAGGATGGC[A/G]TAAGCCCAGGAGTTT | 6612 |
rs181037272 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SUMO3 | GRCh38.p7 | 21:44809298 | GCATTCTGATATGCA[A/G]ATTTATGATCCAGCT | 6612 |
rs181156517 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SUMO3 | GRCh38.p7 | 21:44815515 | CCATCTCCCCATCCC[A/G]AATGTGGCCTCCAGC | 6612 |
rs181548221 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SUMO3 | GRCh38.p7 | 21:44807220 | GGAAGAGGCATTGCT[A/G]TATGCTCACTACAGC | 6612 |
rs181635780 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SUMO3 | GRCh38.p7 | 21:44812527 | CGTTCAGCCATGCAG[A/T]GTCTCAAAGACGCTG | 6612 |
rs181777960 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | SUMO3 | GRCh38.p7 | 21:44808309 | CAAGGTCAGGAGATC[A/G]AGACCATCCTGGCTA | 6612 |
rs182459167 | snp | A/C | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44817889 | GGGTGGGGGCGGAGC[A/C]GGGCTGGGGGCGGGA | 6612 |
rs182701893 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | SUMO3 | GRCh38.p7 | 21:44810047 | CCACCATGACTTTGG[A/C]CTTGAGGAGGGCAGC | 6612 |
rs183296066 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SUMO3 | GRCh38.p7 | 21:44810220 | AAACCCCACTGAAAT[A/G]AAGTAAATGAAAAAG | 6612 |
rs183819497 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SUMO3 | GRCh38.p7 | 21:44815935 | TATCCAGGGAAGTCA[G/T]AACCATTCTCCTGCC | 6612 |
rs183924957 | snp | C/T | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44817020 | CACTGGGGGACGCGA[C/T]GGGGAGGGGTGAGCA | 6612 |
rs184052238 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | SUMO3 | GRCh38.p7 | 21:44812166 | GGCTCAAACAATCCT[C/T]CCACCTCAGCCTCCT | 6612 |
rs184180810 | snp | A/G | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44807448 | CTTTATACCAAGTGC[A/G]GGGGACCATGCCATG | 6612 |
rs184681415 | snp | C/G | 0.00557542 | 0.0525036 | utr-variant-3-prime | SUMO3 | GRCh38.p7 | 21:44806817 | TGAGTTGCACTTGAA[C/G]TACATCAAAGAGAGG | 6612 |
rs184965500 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | SUMO3 | GRCh38.p7 | 21:44805730 | CCCGAGCCCATACAG[C/T]AAACAGGAAATGAGA | 6612 |
rs185162998 | snp | A/C | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44810982 | CACCCATGCACACAC[A/C]CATGCACACACCCAC | 6612 |
rs185486290 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | SUMO3 | GRCh38.p7 | 21:44819130 | CTGGGAAAGGCTCAG[A/C]CAACTGAGCAACGTC | 6612 |
rs185504091 | snp | A/C | 5.41638e-05 | 0.00520375 | splice-donor-variant, intron-variant | SUMO3 | GRCh38.p7 | 21:44813860 | ATCCACGAAGAGGGC[A/C]CCTCGGGCAGCTGCA | 6612 |
rs185631313 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | SUMO3 | GRCh38.p7 | 21:44819432 | TCCGAGGGGACGTGG[C/T]GCCTCAGAGCCCACA | 6612 |
rs185743361 | snp | G/T | 0.00835141 | 0.0640778 | upstream-variant-2KB | SUMO3 | GRCh38.p7 | 21:44820122 | ATTGCTGACATGAAA[G/T]CTCGACCCACATGTG | 6612 |
rs185804360 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SUMO3 | GRCh38.p7 | 21:44815545 | CACAGAGACAACTGG[A/C]CTAGGAAGGAAGAGC | 6612 |
rs185911602 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SUMO3 | GRCh38.p7 | 21:44814874 | AACAATGGCACAATC[A/G]GGGTGTCTTGTTGCC | 6612 |
rs186325194 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SUMO3 | GRCh38.p7 | 21:44809666 | ACACGTCACAGTGAC[A/G]CTAGCTCAGACAGCT | 6612 |
rs187154289 | snp | A/G/T | 0.00358779 | 0.0422022 | upstream-variant-2KB | SUMO3 | GRCh38.p7 | 21:44818830 | GGACGCGGGAAACGC[A/G/T]CTGGGCCGGCAGGAC | 6612 |
rs187170345 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | SUMO3 | GRCh38.p7 | 21:44816078 | CAGAAGCGGGGCCTG[G/T]GAGGTGGCAGCCACT | 6612 |
rs187394548 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | SUMO3 | GRCh38.p7 | 21:44810089 | CACGCAGCCTTTCTG[C/T]GTCCTGAGGGAATGG | 6612 |
rs187503712 | snp | A/C | | | utr-variant-3-prime | SUMO3 | GRCh38.p7 | 21:44806236 | ATCCTTGCCTGTGTA[A/C]CAACGCCAGGTACTG | 6612 |
rs187516208 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | SUMO3 | GRCh38.p7 | 21:44805725 | TCCCACCCGAGCCCA[A/T]ACAGCAAACAGGAAA | 6612 |
rs187569757 | snp | C/T | 0.000345722 | 0.0131431 | intron-variant | SUMO3 | GRCh38.p7 | 21:44808509 | AACAAAGCGAGACTC[C/T]GTCTCAAAAAAAAAA | 6612 |
rs187605563 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | SUMO3 | GRCh38.p7 | 21:44811504 | TTGAGCCCCAGGGCT[C/G]AAGGCTGCAGTGAAC | 6612 |
rs187742411 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SUMO3 | GRCh38.p7 | 21:44817506 | CGTGCACTCGACACA[A/G]GATCCCGCACCCAGG | 6612 |
rs188193224 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | SUMO3 | GRCh38.p7 | 21:44819770 | CCAGGCTATAAGACA[A/G]TGGTGGTCTGAATTC | 6612 |
rs188835085 | snp | A/G | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44812427 | CATGGCTGACCTCTG[A/G]AATAAAAAAGAAAAA | 6612 |
rs188978703 | snp | A/G/T | 0.00835444 | 0.0641245 | intron-variant | SUMO3 | GRCh38.p7 | 21:44808255 | CGTTGGCTCATGCCT[A/G/T]TAATCCCAGCACTTT | 6612 |
rs189188956 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SUMO3 | GRCh38.p7 | 21:44810596 | TGTGCGCCAAGTCCC[C/T]TCTCCCCTCCAGATG | 6612 |
rs189900052 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SUMO3 | GRCh38.p7 | 21:44815125 | TGCCCTCAGGAAGCA[C/T]TGTACATCACACGCC | 6612 |
rs190004210 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | SUMO3 | GRCh38.p7 | 21:44807152 | GACACTAGCGACATC[A/G]CCTGGTCACACCTTG | 6612 |
rs190013220 | snp | A/G | 0.00716266 | 0.059414 | upstream-variant-2KB | SUMO3 | GRCh38.p7 | 21:44819264 | CTGCTGAAGTCTTTC[A/G]GGGAGAGGGTCTGAG | 6612 |
rs190354183 | snp | A/C | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44811056 | CACACACGCACACAC[A/C]CACACATACACACAC | 6612 |
rs190569933 | snp | A/G | 0.0383715 | 0.133092 | intron-variant | SUMO3 | GRCh38.p7 | 21:44815749 | AATGGCTGCAGCCCC[A/G]GGAGAGGCTGGGGCA | 6612 |
rs190703603 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SUMO3 | GRCh38.p7 | 21:44808807 | CCCCGCTTCCCTTAC[A/G]GTGAGGACGGGCCCA | 6612 |
rs190809365 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SUMO3 | GRCh38.p7 | 21:44814280 | TTTACACAGAATTTA[C/T]TTTTAACTTCCACTT | 6612 |
rs191227970 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | SUMO3 | GRCh38.p7 | 21:44809912 | TCTTTCCAGAAGCCG[A/C]GTAGAACTTCTACAA | 6612 |
rs191519187 | snp | C/G/T | 0.0267878 | 0.112589 | intron-variant | SUMO3 | GRCh38.p7 | 21:44812119 | GCTGGAGCAGTGATA[C/G/T]GACCTCAGCTCCCTG | 6612 |
rs192067991 | snp | A/G | 0.0228947 | 0.104514 | upstream-variant-2KB | SUMO3 | GRCh38.p7 | 21:44819072 | GCTGGGAAATGGCAG[A/G]GCCTGGATTTGAACC | 6612 |
rs192099380 | snp | A/T | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44816992 | GGGGACGCGATGGAT[A/T]GGGGTGGGCGCACAC | 6612 |
rs192275904 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SUMO3 | GRCh38.p7 | 21:44810661 | CAACTCTCAAACTGT[A/G]GCATCTGGGCGCCTC | 6612 |
rs192371457 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | SUMO3 | GRCh38.p7 | 21:44805729 | ACCCGAGCCCATACA[G/T]CAAACAGGAAATGAG | 6612 |
rs192768583 | snp | C/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | SUMO3 | GRCh38.p7 | 21:44806481 | TGCCTGTAACAGCAA[C/G]TGACAGTCTGTCCTC | 6612 |
rs193216964 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | SUMO3 | GRCh38.p7 | 21:44819404 | CTGGGAGGGGGCTCC[A/G]CAACCAGCCCCTTCC | 6612 |
rs199941641 | in-del | -/AG | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44811047 | CCCACATACACACAC[-/AG]GCACACACCCACACA | 6612 |
rs200233961 | snp | C/T | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44810498 | CCACGGCAGCACACA[C/T]GAGATGTGCTTTCTG | 6612 |
rs200472105 | snp | A/C/T | 0.000233425 | 0.010801 | synonymous-codon, intron-variant | SUMO3 | GRCh38.p7 | 21:44813955 | CACGGGGAGGCTCTG[A/C/T]GGGGGAGCAAGGTGC | 6612 |
rs200613139 | in-del | -/TCGGGC | | | upstream-variant-2KB | SUMO3 | GRCh38.p7 | 21:44818236 | TCCCGCGCGACCCCG[-/TCGGGC]GCGGAAGCCCTAGGG | 6612 |
rs200616849 | snp | C/T | 0.00422768 | 0.0457817 | utr-variant-3-prime | SUMO3 | GRCh38.p7 | 21:44806887 | CCTTTGTGGTCGGCA[C/T]GGTCACGTGCTCACC | 6612 |
rs200803487 | snp | C/T | 0.000164807 | 0.00907614 | intron-variant | SUMO3 | GRCh38.p7 | 21:44809139 | AAGGAAAAGCAGTGG[C/T]CATTAGTCTCACTGG | 6612 |
rs200891454 | in-del | -/C | 0.00636936 | 0.0560724 | intron-variant | SUMO3 | GRCh38.p7 | 21:44812759 | GGGGGAAGGGCAGAG[-/C]CCCCCCCCACATGTA | 6612 |
rs201436958 | snp | C/G | 1.65597e-05 | 0.00287743 | synonymous-codon | SUMO3 | GRCh38.p7 | 21:44813991 | CTGCCTCTCGCAGTA[C/G]GCCTTCATCAGCTTG | 6612 |
rs201522032 | snp | C/T | 5.11139e-05 | 0.00505513 | utr-variant-3-prime | SUMO3 | GRCh38.p7 | 21:44806927 | CAATGCGAGGATGGA[C/T]GGCCCGGGCTGGGGA | 6612 |
rs201608002 | in-del | -/CCCATG | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44810981 | ACACCCATGCACACA[-/CCCATG]CACACACCCACACAT | 6612 |
rs201757654 | snp | A/C | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44811142 | CACACAGGCACACAC[A/C]CACACATACACACAC | 6612 |
rs367719710 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | SUMO3 | GRCh38.p7 | 21:44807052 | CCAGCTGTCATGGTT[A/G]TCACAACAGGCACAG | 6612 |
rs367739728 | in-del | -/GGCACACACCCACACACA | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44811184 | ACACATACACACACA[-/GGCACACACCCACACACA]TGCACAAAGACACGG | 6612 |
rs367781202 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | SUMO3 | GRCh38.p7 | 21:44812716 | AAGCAGCAGTGCAGG[C/T]GGGGCAGGAGGGGAG | 6612 |
rs367829457 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SUMO3 | GRCh38.p7 | 21:44814307 | ACTTGTTAAGCATCC[A/G]TGTGTAAAACAATGC | 6612 |
rs368110579 | snp | A/G | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44815212 | GATGCCTAAATACAG[A/G]GAGTGGGATGTAGAA | 6612 |
rs368198109 | snp | C/G | 5.02021e-05 | 0.00500984 | utr-variant-3-prime | SUMO3 | GRCh38.p7 | 21:44806939 | GGACGGCCCGGGCTG[C/G]GGACGGGCCCTCTAG | 6612 |
rs368345123 | snp | A/G | | | utr-variant-3-prime | SUMO3 | GRCh38.p7 | 21:44806193 | TTCAATATTAAGAGG[A/G]AGAAAAAGGCCAATT | 6612 |
rs368364423 | snp | A/G | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44811290 | CAATCAATTGCTACT[A/G]AGGATGGGTGCGGTG | 6612 |
rs368428785 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | SUMO3 | GRCh38.p7 | 21:44817448 | GGCCCCTCAGAGCGC[G/T]CCCCTTGGGGGTAAC | 6612 |
rs368636514 | snp | A/G | 1.69766e-05 | 0.00291342 | utr-variant-3-prime | SUMO3 | GRCh38.p7 | 21:44806928 | AATGCGAGGATGGAC[A/G]GCCCGGGCTGGGGAC | 6612 |
rs368691993 | in-del | -/TGCACACACGCACACACCCACATA | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44811017 | GCACACACCCACATA[-/TGCACACACGCACACACCCACATA]CACACACGCACACAC | 6612 |
rs368758616 | snp | A/G | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44817873 | ACGCGGGGCGGAGTC[A/G]GGGTGGGGGCGGAGC | 6612 |
rs368846598 | snp | A/G/T | 0.000232648 | 0.0107832 | synonymous-codon, missense, intron-variant | SUMO3 | GRCh38.p7 | 21:44813972 | GGGGAGCAAGGTGCC[A/G/T]CACCTGCCTCTCGCA | 6612 |
rs368931038 | snp | C/T | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44815698 | GATGCAGGGCCCAGA[C/T]GTCCCCCACAGGGTA | 6612 |
rs368938411 | snp | C/T | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44810569 | GCCCACGAAAGCGCG[C/T]GCCCTCAACACTGTG | 6612 |
rs369290331 | snp | A/G | 3.29592e-05 | 0.00405938 | intron-variant | SUMO3 | GRCh38.p7 | 21:44809129 | AAGCCCTGGAAAGGA[A/G]AAGCAGTGGCCATTA | 6612 |
rs369413991 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SUMO3 | GRCh38.p7 | 21:44814923 | TGAGGCAAAAAGCTG[A/T]TGTCAAGAGACTGGG | 6612 |
rs369635137 | snp | A/C/G/T | 0.000133345 | 0.00816447 | missense, intron-variant | SUMO3 | GRCh38.p7 | 21:44813956 | ACGGGGAGGCTCTGC[A/C/G/T]GGGGAGCAAGGTGCC | 6612 |
rs369713183 | snp | A/T | | | upstream-variant-2KB | SUMO3 | GRCh38.p7 | 21:44819155 | AACGTCGCAAAGCCA[A/T]GGAGACAAGTCTTCA | 6612 |
rs369793646 | snp | C/G | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44807858 | CCCCAGAGACTCCAC[C/G]AGGCCCTCCCTGCTC | 6612 |
rs369827875 | snp | A/G | 3.45107e-05 | 0.00415381 | utr-variant-3-prime | SUMO3 | GRCh38.p7 | 21:44806920 | TCAACAGCAATGCGA[A/G]GATGGACGGCCCGGG | 6612 |
rs369832102 | snp | A/G | 1.68783e-05 | 0.00290498 | intron-variant | SUMO3 | GRCh38.p7 | 21:44807069 | CACAACAGGCACAGC[A/G]AGAGAGAGGGGAGCC | 6612 |
rs369996303 | snp | C/T | 0.00279162 | 0.0372561 | utr-variant-3-prime | SUMO3 | GRCh38.p7 | 21:44806307 | CTGGGCCTCAGACCC[C/T]GAGGTTACATGCTTG | 6612 |
rs370151478 | snp | A/G | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44812466 | AACCGAGAATATTAC[A/G]TGCAGCCACATACTG | 6612 |
rs370251385 | snp | A/G | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44817059 | GGGTGTGATGGAGAG[A/G]GCGACGCAATAGGGA | 6612 |
rs370484736 | snp | A/G | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44817278 | GCGATGGGTGGGAGT[A/G]GGTGCACACTGAGGG | 6612 |
rs370649492 | snp | C/T | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44811099 | ATGCACACACCCACA[C/T]ACACACACATGCACA | 6612 |
rs370756017 | snp | A/G | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44808748 | GCTACAACAGCAAGC[A/G]TCCAGACAATGAGTG | 6612 |
rs370894712 | snp | A/G | 0.0225045 | 0.103662 | intron-variant | SUMO3 | GRCh38.p7 | 21:44811048 | CCCACATACACACAC[A/G]CACACACCCACACAT | 6612 |
rs371061129 | snp | G/T | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44812077 | TTTTTTTTTTTTTTT[G/T]AGACAGGGTCTTGCT | 6612 |
rs371677692 | in-del | -/AC | 0.00318978 | 0.0398085 | upstream-variant-2KB | SUMO3 | GRCh38.p7 | 21:44819612 | TTGTGGAAGTGAGAA[-/AC]ACGCAGCTTAGAAAT | 6612 |
rs371816941 | snp | C/T | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44812826 | GAGAACATGGGCACC[C/T]GGGAAGTCACACACA | 6612 |
rs371905158 | snp | C/G | 0.00038252 | 0.0138244 | missense, intron-variant | SUMO3 | GRCh38.p7 | 21:44813966 | TCTGCGGGGGAGCAA[C/G]GTGCCGCACCTGCCT | 6612 |
rs371961293 | snp | C/G | | | upstream-variant-2KB | SUMO3 | GRCh38.p7 | 21:44819078 | AAATGGCAGGGCCTG[C/G]ATTTGAACCTAAGCG | 6612 |
rs372086437 | snp | C/T | 0.000943354 | 0.0216976 | intron-variant | SUMO3 | GRCh38.p7 | 21:44809008 | TTACCCCGCACAAAT[C/T]GGAAGTCGCCCTGGA | 6612 |
rs372124158 | snp | C/T | 8.3515e-05 | 0.00646146 | utr-variant-3-prime | SUMO3 | GRCh38.p7 | 21:44806943 | GGCCCGGGCTGGGGA[C/T]GGGCCCTCTAGAAAC | 6612 |
rs372210955 | in-del | -/AC/TG | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44811040 | GCACACACCCACATA[-/AC/TG]CACACACGCACACAC | 6612 |
rs372270541 | snp | A/G | | | upstream-variant-2KB | SUMO3 | GRCh38.p7 | 21:44818258 | CGGAAGCCCTAGGGC[A/G]CTGTGGGGCGCGGGC | 6612 |
rs372273961 | snp | C/T | | | utr-variant-3-prime | SUMO3 | GRCh38.p7 | 21:44806812 | AGTTTTGAGTTGCAC[C/T]TGAAGTACATCAAAG | 6612 |
rs372480180 | snp | A/G | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44807648 | TCTAAGCAAGAGGAA[A/G]CTTCTGCCAGTTCCT | 6612 |
rs372559917 | snp | C/G | 1.68943e-05 | 0.00290635 | intron-variant | SUMO3 | GRCh38.p7 | 21:44807071 | CAACAGGCACAGCGA[C/G]AGAGAGGGGAGCCTG | 6612 |
rs372644452 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SUMO3 | GRCh38.p7 | 21:44815483 | GGCGGCAGCCTGAGT[A/G]GTGAGCTGGCACACC | 6612 |
rs372781522 | snp | A/G | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44817525 | CCCGCACCCAGGGCG[A/G]TGCCGGGGGAGAGGG | 6612 |
rs372856053 | snp | C/G/T | 3.32492e-05 | 0.00407722 | intron-variant | SUMO3 | GRCh38.p7 | 21:44809028 | GTCGCCCTGGAACCA[C/G/T]GCGAAGCCAGCTCCG | 6612 |
rs372923043 | snp | G/T | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44816167 | ATGGCAGAGCTAAGT[G/T]TAAATACTGCTGAGA | 6612 |
rs373168113 | snp | A/G | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44810718 | CCCATGTGGATGCAC[A/G]GCCCTGGCAGCACAG | 6612 |
rs373252768 | snp | A/G | 8.28576e-05 | 0.00643599 | synonymous-codon | SUMO3 | GRCh38.p7 | 21:44813985 | CCGCACCTGCCTCTC[A/G]CAGTAGGCCTTCATC | 6612 |
rs373397038 | snp | A/G | | | downstream-variant-500B | SUMO3 | GRCh38.p7 | 21:44805264 | CAAACACCAGAAAAC[A/G]AGAGATGTCCTAGAC | 6612 |
rs373524329 | snp | A/G/T | 0.00398691 | 0.0444912 | intron-variant | SUMO3 | GRCh38.p7 | 21:44815278 | TGCTTGCTTCCCTGG[A/G/T]GTATGCACCCTGGGG | 6612 |
rs373705438 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SUMO3 | GRCh38.p7 | 21:44807626 | CCACCCTGATCTTCT[C/T]CCATCCTCTAAGCAA | 6612 |
rs373981386 | snp | A/G | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44808327 | ACCATCCTGGCTAAC[A/G]TGGTGAAACCCCGTC | 6612 |
rs374174613 | snp | C/T | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44812582 | ACCCTGGAGGATGTG[C/T]TCCACCACAAAACAC | 6612 |
rs374675274 | snp | A/C | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44811176 | CACACACCCACACAT[A/C]CACACACATGCACAA | 6612 |
rs374679104 | snp | A/G | 0.00398564 | 0.0444627 | upstream-variant-2KB | SUMO3 | GRCh38.p7 | 21:44818402 | CCGGGGCCGCCGCCC[A/G]TGGCCGCAGGGACCT | 6612 |
rs375002240 | snp | A/G | 0.00104736 | 0.02286 | synonymous-codon, intron-variant | SUMO3 | GRCh38.p7 | 21:44813967 | CTGCGGGGGAGCAAG[A/G]TGCCGCACCTGCCTC | 6612 |
rs375202216 | snp | A/C | 1.79903e-05 | 0.00299914 | intron-variant | SUMO3 | GRCh38.p7 | 21:44809006 | AGTTACCCCGCACAA[A/C]TCGGAAGTCGCCCTG | 6612 |
rs375352091 | snp | C/T | 1.68516e-05 | 0.00290268 | missense, intron-variant | SUMO3 | GRCh38.p7 | 21:44813942 | GGACCAGTGCGCACA[C/T]GGGGAGGCTCTGCGG | 6612 |
rs375372311 | snp | C/T | | | upstream-variant-2KB | SUMO3 | GRCh38.p7 | 21:44819101 | CCTAAGCGTCTGAGC[C/T]GTTTCTGTCCTGCCT | 6612 |
rs375578914 | snp | C/G | 0.000153988 | 0.00877328 | intron-variant | SUMO3 | GRCh38.p7 | 21:44814122 | GCAGAAGACACCAGA[C/G]ACTGGCCTCAAAACT | 6612 |
rs375714436 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | SUMO3 | GRCh38.p7 | 21:44813649 | CAGACCTGAGCAGGG[A/C]CCCCAAGAGCCTTCA | 6612 |
rs375748622 | snp | C/G/T | 8.81634e-05 | 0.00663892 | utr-variant-3-prime | SUMO3 | GRCh38.p7 | 21:44806917 | CATTCAACAGCAATG[C/G/T]GAGGATGGACGGCCC | 6612 |
rs375792326 | snp | A/G | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44815369 | GCAGTGAGGGGCTCC[A/G]GCTGCGAGCCTGAAG | 6612 |
rs375860938 | snp | A/G | 0.000115524 | 0.00759925 | intron-variant | SUMO3 | GRCh38.p7 | 21:44809043 | CGCGAAGCCAGCTCC[A/G]TACCTGTGCTGGAGT | 6612 |
rs375985410 | in-del | -/TACACACA | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44811175 | GCACACACCCACACA[-/TACACACA]CATGCACAAAGACAC | 6612 |
rs375990826 | snp | A/G | 0.00318978 | 0.0398085 | upstream-variant-2KB | SUMO3 | GRCh38.p7 | 21:44819385 | GTGGCCAGCTCAGAC[A/G]GTCCTGGGAGGGGGC | 6612 |
rs376041663 | in-del | -/GCACACAC | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44811009 | CACACATGCACACAC[-/GCACACAC]CCACATATGCACACA | 6612 |
rs376127177 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SUMO3 | GRCh38.p7 | 21:44811302 | ACTGAGGATGGGTGC[A/G]GTGGCTCACACCTGT | 6612 |
rs376262470 | snp | C/T | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44807431 | CCCACAGGAGCCTTG[C/T]GCTTTATACCAAGTG | 6612 |
rs376372327 | snp | A/G | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44809757 | GGGGAGGGGAAATGA[A/G]CCGCCAGGTGAATAC | 6612 |
rs376716020 | snp | C/T | 6.68673e-05 | 0.0057818 | intron-variant | SUMO3 | GRCh38.p7 | 21:44807045 | TCCATCTCCAGCTGT[C/T]ATGGTTGTCACAACA | 6612 |
rs376770699 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SUMO3 | GRCh38.p7 | 21:44814342 | CTAGGGTCCTCTGAC[A/G]TTGTTAATTCAAAGA | 6612 |
rs376849017 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | SUMO3 | GRCh38.p7 | 21:44810526 | CTGAGAAGGTGGGTG[C/G]GGAGCTCCAGGCGCA | 6612 |
rs376946342 | snp | A/G | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44812805 | CTGCCATCCCGCAGC[A/G]CAGAGGAGAACATGG | 6612 |
rs377183705 | snp | A/C | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44810950 | CACCCACACACATGC[A/C]CACACCCACACATGC | 6612 |
rs377224734 | snp | A/C | 0.000365564 | 0.0135147 | intron-variant | SUMO3 | GRCh38.p7 | 21:44808519 | GACTCCGTCTCAAAA[A/C]AAAAAGTCTGTTTCC | 6612 |
rs377336255 | snp | A/G | | | upstream-variant-2KB | SUMO3 | GRCh38.p7 | 21:44819551 | GTAGGTAGCACAGAC[A/G]CACTAAACTCCGGCA | 6612 |
rs377417594 | snp | A/G | | | downstream-variant-500B | SUMO3 | GRCh38.p7 | 21:44805545 | CAGTGGCTGCCTGGA[A/G]TGGTCAATTCAAACA | 6612 |
rs377763896 | snp | A/G | | | downstream-variant-500B | SUMO3 | GRCh38.p7 | 21:44805341 | ACGAAACCCAGGAGA[A/G]GGAGGGTAACATGTC | 6612 |
rs386394862 | in-del | -/TTT | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44812054 | CTGAACTTCTCACCT[-/TTT]TTTTTTTTTTTTTTT | 6612 |
rs398036492 | in-del | -/AC | 0 | 0 | intron-variant | SUMO3 | GRCh38.p7 | 21:44813396 | CAGACACACACACAC[-/AC]CACGTCACAAACAGC | 6612 |
rs527525220 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | SUMO3 | GRCh38.p7 | 21:44815777 | GCAGGGCAGGGCCGG[A/C]CACAGTGCCTCTGCT | 6612 |
rs527599216 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SUMO3 | GRCh38.p7 | 21:44810867 | GAGCGCAGAGGAGAA[C/T]GGACAGGAAGGAGGC | 6612 |
rs527853742 | snp | A/G | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44809643 | CGAAACCCAGGTGAG[A/G]AAGCGTAACACGTCA | 6612 |
rs528177574 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SUMO3 | GRCh38.p7 | 21:44808398 | GGCACCTATAGTCCC[A/G]GCTACTTGGGAGGCT | 6612 |
rs528261769 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SUMO3 | GRCh38.p7 | 21:44810318 | AGAGGCTACTGAGGC[A/G]TGGACACTGGTGGTC | 6612 |
rs528693051 | snp | A/C | 0.000798403 | 0.0199641 | upstream-variant-2KB | SUMO3 | GRCh38.p7 | 21:44818644 | CCGGGCCCTCCACAC[A/C]CGTCCTCAAGAAGAC | 6612 |
rs528731533 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | SUMO3 | GRCh38.p7 | 21:44819125 | CCTGCCTGGGAAAGG[C/T]TCAGCCAACTGAGCA | 6612 |
rs528792530 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SUMO3 | GRCh38.p7 | 21:44813579 | AGGCCAGCTCATACG[C/T]GAGGACAGGGTGACA | 6612 |
rs528833700 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | SUMO3 | GRCh38.p7 | 21:44808316 | AGGAGATCGAGACCA[G/T]CCTGGCTAACATGGT | 6612 |
rs528952810 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SUMO3 | GRCh38.p7 | 21:44817234 | CGCACACCGGGGGAC[A/G]CGATGGAGGCGGTGG | 6612 |
rs528987071 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SUMO3 | GRCh38.p7 | 21:44817693 | GGCGCGCGCCTTCCC[A/G]GCTGGGGAGGAGACG | 6612 |
rs528995416 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SUMO3 | GRCh38.p7 | 21:44811464 | GGAGTCCCACCTACT[C/T]GGGAGGCTGAGGTGG | 6612 |
rs529261490 | in-del | -/A | 0.0023933 | 0.0345097 | utr-variant-3-prime | SUMO3 | GRCh38.p7 | 21:44806073 | AATTCAGCAATACTT[-/A]AGTCTTACTTTTTTA | 6612 |
rs529652832 | snp | C/T | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44813444 | CCAGCTGGGCACTGC[C/T]AGTGGGGCAGCTCAT | 6612 |
rs529737891 | snp | C/T | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44815299 | CACCCTGGGGAGACC[C/T]TGGGGAGGCATGGTG | 6612 |
rs529912403 | in-del | -/AAC | 0.0119091 | 0.0762411 | intron-variant | SUMO3 | GRCh38.p7 | 21:44812393 | GAACTTTTCACTTTT[-/AAC]AACATTGGGAGCTAT | 6612 |
rs530144172 | snp | C/T | 8.26658e-05 | 0.00642854 | synonymous-codon | SUMO3 | GRCh38.p7 | 21:44814015 | CAGCTTGCTCAGCGG[C/T]GTGTGCCTCTTGATC | 6612 |
rs530314079 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SUMO3 | GRCh38.p7 | 21:44809166 | CTGGCAAGCCCTGGA[A/G]AGGAAAAGCAGTGGC | 6612 |
rs530639204 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | SUMO3 | GRCh38.p7 | 21:44807902 | AGCTTCTCCCTGGTG[A/T]ACACTCCCAGAGCTG | 6612 |
rs530734138 | snp | A/G | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44808529 | CAAAAAAAAAAGTCT[A/G]TTTCCAGGTCCAAAG | 6612 |
rs530854866 | snp | A/G | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44811354 | CGAGGCAGAAGGATC[A/G]CTTAAGCCCAGGAAT | 6612 |
rs531209061 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime | SUMO3 | GRCh38.p7 | 21:44818059 | GCTCTCCCGCCGCAA[C/T]TGTGCGCGGGGCCGC | 6612 |
rs531438835 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SUMO3 | GRCh38.p7 | 21:44816640 | AAGGGCTTCGGAAAG[A/G]TTCTCTTTTTATGAA | 6612 |
rs531442627 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SUMO3 | GRCh38.p7 | 21:44810919 | GCACACACATGCCCA[C/T]ACCCACACATGCCCA | 6612 |
rs531816374 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SUMO3 | GRCh38.p7 | 21:44815623 | CCCCTTCACTTCCCC[A/C]AGCATGAGGATGCAC | 6612 |
rs531820530 | snp | C/G/T | 0.00119737 | 0.0244387 | intron-variant | SUMO3 | GRCh38.p7 | 21:44809943 | TGCTGGCACCACTAC[C/G/T]TCCCCCCTTTACAAA | 6612 |
rs531861841 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SUMO3 | GRCh38.p7 | 21:44810405 | GAGGCAGAGCTGTGG[C/T]AGGCAGCTGATTCTG | 6612 |
rs532257043 | in-del | -/AGAATC | 0.00119737 | 0.0244387 | intron-variant | SUMO3 | GRCh38.p7 | 21:44812026 | ACAAACAAAGCACAG[-/AGAATC]AGAATCCACTGAACT | 6612 |
rs532609886 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SUMO3 | GRCh38.p7 | 21:44813687 | AGACTTCACAGATGT[C/T]AGTACCCCATGGAGA | 6612 |
rs532679665 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SUMO3 | GRCh38.p7 | 21:44808501 | GCCTGGGCAACAAAG[C/T]GAGACTCCGTCTCAA | 6612 |
rs532820884 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SUMO3 | GRCh38.p7 | 21:44808241 | GTTTCGGCCGGGCGC[A/G]TTGGCTCATGCCTTT | 6612 |
rs532999707 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SUMO3 | GRCh38.p7 | 21:44817786 | CGGGGGCAGAGGGGG[C/G]GCACCTTGGGCGGGC | 6612 |
rs533035723 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SUMO3 | GRCh38.p7 | 21:44812454 | AAAAAAAGTTTCAAC[C/T]GAGAATATTACGTGC | 6612 |
rs533039230 | snp | A/G | 0.00473828 | 0.0484426 | utr-variant-3-prime | SUMO3 | GRCh38.p7 | 21:44806880 | GCAGACACCTTTGTG[A/G]TCGGCATGGTCACGT | 6612 |
rs533258368 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | SUMO3 | GRCh38.p7 | 21:44805342 | CGAAACCCAGGAGAG[A/G]GAGGGTAACATGTCA | 6612 |
rs533652851 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SUMO3 | GRCh38.p7 | 21:44809436 | GGCTCATTTTCAACC[C/T]AGGTTTTGTTACACC | 6612 |
rs533673279 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SUMO3 | GRCh38.p7 | 21:44817288 | GGAGTAGGTGCACAC[A/T]GAGGGCACGATTGGG | 6612 |
rs533978258 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SUMO3 | GRCh38.p7 | 21:44808308 | ACAAGGTCAGGAGAT[C/G]GAGACCATCCTGGCT | 6612 |
rs534277091 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SUMO3 | GRCh38.p7 | 21:44808795 | TGGTCCTTGCACCCC[C/T]GCTTCCCTTACAGTG | 6612 |
rs534761002 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SUMO3 | GRCh38.p7 | 21:44817460 | CGCGCCCCTTGGGGG[A/T]AACCCCAGACGCTTG | 6612 |
rs534845017 | snp | C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | SUMO3 | GRCh38.p7 | 21:44818974 | CCCTCAGGAGTGCCC[C/G]GGTGGTGCCAGCCGG | 6612 |
rs534881772 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | SUMO3 | GRCh38.p7 | 21:44819351 | GAGCCCAGGGCCTCA[A/G]CAGAGGATGTGGAGG | 6612 |
rs534884332 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | SUMO3 | GRCh38.p7 | 21:44818163 | CGCTCCCCGGGGCGT[C/T]GGGCGCGCGCAGGCC | 6612 |
rs535137437 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SUMO3 | GRCh38.p7 | 21:44816703 | AAGGAATGGCCAGTG[C/T]ACCTGAATGCAGGGT | 6612 |
rs535175407 | snp | C/T | 0.0995161 | 0.199636 | intron-variant | SUMO3 | GRCh38.p7 | 21:44811015 | ATGCACACACCCACA[C/T]ATGCACACACGCACA | 6612 |
rs535335481 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SUMO3 | GRCh38.p7 | 21:44807200 | CACTGCAGCTCAGCA[C/T]GCATGGAAGAGGCAT | 6612 |
rs535427702 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | SUMO3 | GRCh38.p7 | 21:44815982 | CTTTCCAGCACCACC[C/G]GGCCCCAGAGTCCAC | 6612 |
rs535468397 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SUMO3 | GRCh38.p7 | 21:44810693 | AGAACCTGCAATCCA[C/G]ACAGATCACCCCATG | 6612 |
rs535808828 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SUMO3 | GRCh38.p7 | 21:44815374 | GAGGGGCTCCAGCTG[C/T]GAGCCTGAAGGTGCG | 6612 |
rs535819870 | snp | C/T | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44811938 | AGTGAGAAAATCACC[C/T]ACCTCTGAGGCACAT | 6612 |
rs535924183 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | SUMO3 | GRCh38.p7 | 21:44820030 | GGCCAGAGCCCCTCC[A/G]GAGGGTCGCCACACC | 6612 |
rs536057193 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SUMO3 | GRCh38.p7 | 21:44814224 | CCAACCTAATTCTTA[A/C]AATTCTCCAGCAATT | 6612 |
rs536167688 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SUMO3 | GRCh38.p7 | 21:44809996 | TGTGCCAATGAGGGA[C/T]AGATAAGAAGGCTGC | 6612 |
rs536235692 | snp | A/T | | | upstream-variant-2KB | SUMO3 | GRCh38.p7 | 21:44819906 | CCGCTGGTGGACCGA[A/T]CGCCAAGAGGTTTCT | 6612 |
rs536249721 | snp | C/T | 0.00358779 | 0.0422022 | upstream-variant-2KB | SUMO3 | GRCh38.p7 | 21:44818873 | CTTGCGGGCGCCATT[C/T]CTGGGGTGCCTGGCC | 6612 |
rs536433241 | snp | A/C/G | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44810586 | CCCTCAACACTGTGC[A/C/G]CCAAGTCCCCTCTCC | 6612 |
rs536664035 | in-del | -/ACTGGCAT | 0.00119737 | 0.0244387 | intron-variant | SUMO3 | GRCh38.p7 | 21:44807117 | AGTGGGAAGATCCTC[-/ACTGGCAT]ACTGGCATGAGTGTT | 6612 |
rs536671377 | snp | C/T | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44815608 | GACCCCTGCATGAGC[C/T]CCCTTCACTTCCCCA | 6612 |
rs536687499 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | SUMO3 | GRCh38.p7 | 21:44819253 | GAGGGGGAAGGCTGC[C/T]GAAGTCTTTCGGGGA | 6612 |
rs536720223 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SUMO3 | GRCh38.p7 | 21:44813758 | CCACCACACTTCTCC[C/G]AGCCTCTAGGTCCCT | 6612 |
rs536997677 | in-del | -/CA | 0.00636936 | 0.0560724 | intron-variant | SUMO3 | GRCh38.p7 | 21:44811226 | ACACACACCTACACT[-/CA]CGATTCAAATTCTAT | 6612 |
rs537283553 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SUMO3 | GRCh38.p7 | 21:44817363 | GCCGGGACACGATGC[A/G]GAGAAGTGGGTGAAT | 6612 |
rs537345524 | snp | G/T | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44811716 | ACCTCCCGGAAAGAA[G/T]CCCAAATGCAACAAT | 6612 |
rs537633192 | snp | C/T | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44816126 | AACAAGTGTTTTCAA[C/T]GGAACTGGAGCCTGA | 6612 |
rs537748504 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SUMO3 | GRCh38.p7 | 21:44812556 | TGCCCTTCTGTGCCC[A/G]TTCTGACAAGACCCT | 6612 |
rs538283370 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SUMO3 | GRCh38.p7 | 21:44809355 | TACAATCTCTTTCAC[A/G]CGGTGCCTGACACCA | 6612 |
rs538452518 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | SUMO3 | GRCh38.p7 | 21:44819402 | TCCTGGGAGGGGGCT[C/G]CGCAACCAGCCCCTT | 6612 |
rs538674245 | snp | A/C | 0.000798403 | 0.0199641 | upstream-variant-2KB | SUMO3 | GRCh38.p7 | 21:44818375 | GCGTTCCTGGGGCGC[A/C]GGGAAGTGAGGCCGG | 6612 |
rs538711029 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | SUMO3 | GRCh38.p7 | 21:44818773 | CGAGCGCGGGCAAAC[C/T]CAGGCTGGACGCCGC | 6612 |
rs538855487 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | SUMO3 | GRCh38.p7 | 21:44819892 | GGACACAAAGGACAC[C/T]GCTGGTGGACCGAAC | 6612 |
rs538939317 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SUMO3 | GRCh38.p7 | 21:44808815 | CCCTTACAGTGAGGA[C/T]GGGCCCAGCACTTGG | 6612 |
rs539119316 | snp | A/G | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44812827 | AGAACATGGGCACCC[A/G]GGAAGTCACACACAC | 6612 |
rs539136578 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | SUMO3 | GRCh38.p7 | 21:44805527 | AATCAAAGTTTCTCA[A/G]TGCAGTGGCTGCCTG | 6612 |
rs539339685 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | SUMO3 | GRCh38.p7 | 21:44806363 | ATTACCAAAAGACTC[A/G]GTTATTTTTTAACCT | 6612 |
rs539831357 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | SUMO3 | GRCh38.p7 | 21:44820059 | CCTGGCGATGGTCCC[A/G]ACAAGAAGACTCATG | 6612 |
rs539877522 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SUMO3 | GRCh38.p7 | 21:44808421 | GGGAGGCTGAGGCAG[A/G]AGAATGGCGTGAACT | 6612 |
rs539905959 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SUMO3 | GRCh38.p7 | 21:44812246 | AATGTTTCGTAGAGA[C/T]AGGGTCTCCCTGTGT | 6612 |
rs540100627 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SUMO3 | GRCh38.p7 | 21:44816782 | TGGGGGAGACTAAAG[C/T]CCACCCAAGGCTGGA | 6612 |
rs540142409 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SUMO3 | GRCh38.p7 | 21:44811096 | CACATGCACACACCC[A/C]CATACACACACATGC | 6612 |
rs540931661 | snp | A/G | 0.000100172 | 0.00707644 | utr-variant-3-prime | SUMO3 | GRCh38.p7 | 21:44806944 | GCCCGGGCTGGGGAC[A/G]GGCCCTCTAGAAACT | 6612 |
rs541083909 | snp | C/G | 0 | 0 | intron-variant | SUMO3 | GRCh38.p7 | 21:44817695 | CGCGCGCCTTCCCAG[C/G]TGGGGAGGAGACGGG | 6612 |
rs541130264 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SUMO3 | GRCh38.p7 | 21:44811255 | TATGGGAAGTAAAAA[A/C]TACTACTACCTTCAG | 6612 |
rs541220975 | snp | C/T | 0.00199481 | 0.0315187 | upstream-variant-2KB | SUMO3 | GRCh38.p7 | 21:44818566 | CCACCCGCCTCCCTG[C/T]CGCCGCGGTTTCCTG | 6612 |
rs541283545 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SUMO3 | GRCh38.p7 | 21:44813409 | CACCACGTCACAAAC[A/G]GCAGCCAGAAGGCAT | 6612 |
rs541441983 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SUMO3 | GRCh38.p7 | 21:44810839 | CTGTGCAGCAGCCTA[A/G]AGAGGAGGGGAGGAG | 6612 |
rs541458405 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SUMO3 | GRCh38.p7 | 21:44810241 | AATGAAAAAGGCACA[A/G]ACAGGAAGGACAAAG | 6612 |
rs541501756 | snp | C/T | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44815310 | GACCCTGGGGAGGCA[C/T]GGTGCTCTGTCAAGG | 6612 |
rs541540745 | snp | G/T | 0.000399281 | 0.0141238 | downstream-variant-500B | SUMO3 | GRCh38.p7 | 21:44805225 | GGTAAGTTGTCCATG[G/T]CAGAAGGAAAGCTGA | 6612 |
rs542116484 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SUMO3 | GRCh38.p7 | 21:44815512 | CCCCCATCTCCCCAT[A/C]CCGAATGTGGCCTCC | 6612 |
rs542243377 | snp | A/C | 0.000798403 | 0.0199641 | upstream-variant-2KB | SUMO3 | GRCh38.p7 | 21:44819084 | CAGGGCCTGGATTTG[A/C]ACCTAAGCGTCTGAG | 6612 |
rs542280362 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SUMO3 | GRCh38.p7 | 21:44813550 | GCACATGAGGGCAGT[A/G]TCTCTCCAGGGTCAG | 6612 |
rs542437295 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SUMO3 | GRCh38.p7 | 21:44815211 | CGATGCCTAAATACA[A/G]GGAGTGGGATGTAGA | 6612 |
rs542880297 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SUMO3 | GRCh38.p7 | 21:44808861 | GCAAGAATGATGTCT[A/G]CAAAGCAGTTTTCTC | 6612 |
rs543002623 | snp | A/C | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44812996 | AGTCTCACCTTTCGC[A/C]GGTGAAAATAAGATC | 6612 |
rs543255410 | in-del | -/A | 0.00199481 | 0.0315187 | upstream-variant-2KB | SUMO3 | GRCh38.p7 | 21:44819405 | GGGAGGGGGCTCCGC[-/A]AACCAGCCCCTTCCG | 6612 |
rs543272137 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SUMO3 | GRCh38.p7 | 21:44817688 | CGCTGGGCGCGCGCC[C/T]TCCCAGCTGGGGAGG | 6612 |
rs543514762 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SUMO3 | GRCh38.p7 | 21:44816189 | CTGCTGAGAAAATTA[A/G]TATCATATGTATTTT | 6612 |
rs543571104 | snp | A/G | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44807754 | CACCCTGCCACCGAC[A/G]CTATGGGCTGGAGGG | 6612 |
rs543658818 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | SUMO3 | GRCh38.p7 | 21:44818536 | TCGGGCCAGCACCCT[A/G]GACGATTGGGGGCGC | 6612 |
rs543803556 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SUMO3 | GRCh38.p7 | 21:44815138 | CACTGTACATCACAC[A/G]CCTGTTCTCTCCACT | 6612 |
rs543899475 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SUMO3 | GRCh38.p7 | 21:44810450 | AGTTCACATGCAGAC[A/C]CCTCAGGCAGGACCC | 6612 |
rs544049530 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SUMO3 | GRCh38.p7 | 21:44816822 | GTGGGCGCGCATGGT[C/G]GGGGAGGCGCAATGC | 6612 |
rs544062672 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SUMO3 | GRCh38.p7 | 21:44811173 | AGGCACACACCCACA[C/T]ATACACACACATGCA | 6612 |
rs544221711 | snp | A/G | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44817572 | TGACTCAGGAGAGGA[A/G]CACGCAAAGACGCTT | 6612 |
rs544309871 | snp | C/G | | | utr-variant-3-prime | SUMO3 | GRCh38.p7 | 21:44805859 | AGGGAAGGACAATAG[C/G]CAGAACTATGAAAAT | 6612 |
rs544700957 | snp | A/C/G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | SUMO3 | GRCh38.p7 | 21:44818594 | CTGTCAGCCCCAGGC[A/C/G/T]GGGCTCCTTTGGCCA | 6612 |
rs545030418 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SUMO3 | GRCh38.p7 | 21:44812083 | TTTTTTTTTGAGACA[A/G]GGTCTTGCTCTGTCA | 6612 |
rs545048334 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | SUMO3 | GRCh38.p7 | 21:44819033 | AGCCCGGCCGAAGGC[G/T]GGGGAGGCCGCACTT | 6612 |
rs545220518 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SUMO3 | GRCh38.p7 | 21:44813488 | GGGAAGAAGGGGAAA[C/G]AATCACGCGCTTTCT | 6612 |
rs545415206 | snp | C/T | 0.0023933 | 0.0345097 | downstream-variant-500B | SUMO3 | GRCh38.p7 | 21:44805356 | GGGAGGGTAACATGT[C/T]ACAGTGATGCCAGCT | 6612 |
rs545645875 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SUMO3 | GRCh38.p7 | 21:44816999 | CGATGGATAGGGGTG[A/G]GCGCACACTGGGGGA | 6612 |
rs546148365 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SUMO3 | GRCh38.p7 | 21:44810803 | AGTCAGCCTGCGTGA[C/G]AGCAGTCAGGGAAAG | 6612 |
rs546158786 | snp | A/G | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44807572 | TAGTGAAACACCCCC[A/G]CTCACTTCTCTCCTC | 6612 |
rs546325018 | snp | A/G | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44807724 | AGGAGTCCCATCAGG[A/G]CTGTCGGCCACCCTC | 6612 |
rs546408143 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SUMO3 | GRCh38.p7 | 21:44810290 | GGCAGATATGTCAAT[A/G]CTGGGCTGAGCCAGA | 6612 |
rs546569403 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SUMO3 | GRCh38.p7 | 21:44808165 | GTGATGCTTGGTCAC[A/G]GGGCCATCAGCTGAC | 6612 |
rs546726779 | snp | A/G | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44811500 | TCACTTGAGCCCCAG[A/G]GCTCAAGGCTGCAGT | 6612 |
rs546895995 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SUMO3 | GRCh38.p7 | 21:44813139 | AGGAGGAAATCTAAC[C/T]GAAAATCCACAGGCA | 6612 |
rs546962819 | snp | C/T | 0.00159617 | 0.0282053 | upstream-variant-2KB | SUMO3 | GRCh38.p7 | 21:44819804 | TCATGCTGTGTCTGT[C/T]TCCCACACTGTGACC | 6612 |
rs547429190 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SUMO3 | GRCh38.p7 | 21:44817260 | GGTGGGTGCACACGG[A/G]GCGCGATGGGTGGGA | 6612 |
rs547429818 | snp | A/G | | | utr-variant-3-prime | SUMO3 | GRCh38.p7 | 21:44806090 | GTCTTACTTTTTTAT[A/G]TATAGACCATAATCA | 6612 |
rs547463436 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SUMO3 | GRCh38.p7 | 21:44810527 | TGAGAAGGTGGGTGC[A/G]GAGCTCCAGGCGCAG | 6612 |
rs547558810 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | SUMO3 | GRCh38.p7 | 21:44812345 | TCAGCCTCCCAAAGT[A/G]CTGGGATTACAGGCA | 6612 |
rs548141340 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SUMO3 | GRCh38.p7 | 21:44815727 | TAATGGCTGCAGCCC[C/T]GGGGGGAATGGCTGC | 6612 |
rs548416183 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SUMO3 | GRCh38.p7 | 21:44810022 | GCTGCATGAGGCCGG[A/G]GAGCAGTTACCACCA | 6612 |
rs548487708 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SUMO3 | GRCh38.p7 | 21:44814695 | AATCCAACTGAGGAC[A/G]GCCACTCCCCACAGC | 6612 |
rs548524970 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SUMO3 | GRCh38.p7 | 21:44809243 | AAACATTTCCAGATA[C/T]GGCTTAATTCAAAAA | 6612 |
rs548581803 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SUMO3 | GRCh38.p7 | 21:44809437 | GCTCATTTTCAACCC[A/G]GGTTTTGTTACACCA | 6612 |
rs548604998 | snp | C/T | | | upstream-variant-2KB | SUMO3 | GRCh38.p7 | 21:44819944 | ACAGCCAAAGGGGAT[C/T]GAATGGACGGAGGAA | 6612 |
rs548619603 | snp | A/G | 0.00159617 | 0.0282053 | upstream-variant-2KB | SUMO3 | GRCh38.p7 | 21:44819687 | CAGTTGCTGTGTCAC[A/G]AAGTGATGCGTGACT | 6612 |
rs548681956 | snp | A/C | | | upstream-variant-2KB | SUMO3 | GRCh38.p7 | 21:44818485 | ACAGAGCGGAGAAGG[A/C]GGCCCGCGGGGTCCC | 6612 |
rs548988757 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | SUMO3 | GRCh38.p7 | 21:44806824 | CACTTGAAGTACATC[A/G]AAGAGAGGAAAATCA | 6612 |
rs549021637 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SUMO3 | GRCh38.p7 | 21:44807177 | ACCTTGGCTCTTGTC[C/T]GTCCCCTCACTGCAG | 6612 |
rs549030592 | snp | C/T | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44807427 | AGGACCCACAGGAGC[C/T]TTGCGCTTTATACCA | 6612 |
rs549283674 | snp | A/G | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44812032 | AAAGCACAGAGAATC[A/G]GAATCCACTGAACTT | 6612 |
rs549327048 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-5-prime | SUMO3 | GRCh38.p7 | 21:44818125 | GGCACGGGGGTCACG[A/T]GGCTGCGCGCGTTCA | 6612 |
rs549550799 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SUMO3 | GRCh38.p7 | 21:44810932 | CACACCCACACATGC[A/C]CACACCCACACACAT | 6612 |
rs549607402 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | SUMO3 | GRCh38.p7 | 21:44818629 | TCCTACGGGGCTGCC[C/T]CGGGCCCTCCACACC | 6612 |
rs549624442 | snp | A/G | 0.000798403 | 0.0199641 | downstream-variant-500B | SUMO3 | GRCh38.p7 | 21:44805482 | AATGAGCTGCCAGGC[A/G]AATACTAACCTTCCA | 6612 |
rs549889179 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SUMO3 | GRCh38.p7 | 21:44815317 | GGGAGGCATGGTGCT[C/G]TGTCAAGGGAGCTAG | 6612 |
rs549930652 | snp | C/T | 0.0402882 | 0.136092 | intron-variant | SUMO3 | GRCh38.p7 | 21:44817182 | CGTGATGGGGAGGCG[C/T]GGGCGTACACCGGGG | 6612 |
rs550185619 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SUMO3 | GRCh38.p7 | 21:44809357 | CAATCTCTTTCACGC[A/G]GTGCCTGACACCACT | 6612 |
rs550749185 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SUMO3 | GRCh38.p7 | 21:44813722 | AGCACCCCGGGCAGC[C/T]GCCCTGTCAGGAAGA | 6612 |
rs550781821 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SUMO3 | GRCh38.p7 | 21:44808249 | CGGGCGCGTTGGCTC[A/G]TGCCTTTAATCCCAG | 6612 |
rs550901242 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SUMO3 | GRCh38.p7 | 21:44814928 | CAAAAAGCTGATGTC[A/T]AGAGACTGGGAGCCA | 6612 |
rs551097848 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB | SUMO3 | GRCh38.p7 | 21:44819224 | TCACTTTCTTGGCTA[A/G]AGCCCCCACTTAGGA | 6612 |
rs551148903 | snp | C/T | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44811717 | CCTCCCGGAAAGAAG[C/T]CCAAATGCAACAATA | 6612 |
rs551191664 | in-del | -/G | 0.0023933 | 0.0345097 | intron-variant | SUMO3 | GRCh38.p7 | 21:44815584 | AGCTCCAGGCAGGAT[-/G]GAAGTGGGGACCCCT | 6612 |
rs551377668 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SUMO3 | GRCh38.p7 | 21:44811506 | GAGCCCCAGGGCTCA[A/C]GGCTGCAGTGAACCA | 6612 |
rs551383592 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SUMO3 | GRCh38.p7 | 21:44817931 | GACGCGCGTGCAGGC[A/G]GGGTCGCCGCGCTTA | 6612 |
rs551406761 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | SUMO3 | GRCh38.p7 | 21:44808340 | ACATGGTGAAACCCC[A/G]TCTCTACTAAAAATA | 6612 |
rs551416482 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SUMO3 | GRCh38.p7 | 21:44812513 | AAAAGCAAAAGTCAC[A/G]TTCAGCCATGCAGTG | 6612 |
rs551550373 | snp | C/T | 1.68326e-05 | 0.00290104 | intron-variant | SUMO3 | GRCh38.p7 | 21:44807065 | TTGTCACAACAGGCA[C/T]AGCGAGAGAGAGGGG | 6612 |
rs551939147 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SUMO3 | GRCh38.p7 | 21:44815825 | CTGTCCCAGACCCCT[A/G]GTGAATTCCTAATAA | 6612 |
rs551973932 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SUMO3 | GRCh38.p7 | 21:44810612 | TCTCCCCTCCAGATG[C/T]GCCTCCAGGAGGCTG | 6612 |
rs551975982 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SUMO3 | GRCh38.p7 | 21:44816632 | TGCACACCAAGGGCT[C/T]CGGAAAGGTTCTCTT | 6612 |
rs552012624 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SUMO3 | GRCh38.p7 | 21:44810887 | AGGAAGGAGGCAGGA[A/G]AACACTCCCAACACA | 6612 |
rs552152288 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SUMO3 | GRCh38.p7 | 21:44817291 | GTAGGTGCACACTGA[C/G]GGCACGATTGGGGAG | 6612 |
rs553270862 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | SUMO3 | GRCh38.p7 | 21:44805984 | AACCCACGAGAAGAA[C/T]ATGAAGTCATCATTC | 6612 |
rs553350894 | snp | C/T | 0.000798403 | 0.0199641 | missense, intron-variant | SUMO3 | GRCh38.p7 | 21:44813890 | ATCTGGGTCCAGCCC[C/T]GAGACGCTCGTGCTC | 6612 |
rs553532281 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | SUMO3 | GRCh38.p7 | 21:44812559 | CCTTCTGTGCCCGTT[A/C]TGACAAGACCCTGGA | 6612 |
rs553747545 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SUMO3 | GRCh38.p7 | 21:44811045 | ACACCCACATACACA[C/G]ACGCACACACCCACA | 6612 |
rs554108206 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | SUMO3 | GRCh38.p7 | 21:44819489 | GGCAGGCAGGGTTCA[A/G]AGAGTTATCGACTCC | 6612 |
rs554117698 | snp | A/G | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44808816 | CCTTACAGTGAGGAC[A/G]GGCCCAGCACTTGGC | 6612 |
rs554508530 | snp | C/T | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44810738 | TGGCAGCACAGCCAT[C/T]CATGTACACAGCTTT | 6612 |
rs554557893 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SUMO3 | GRCh38.p7 | 21:44807447 | GCTTTATACCAAGTG[C/T]GGGGGACCATGCCAT | 6612 |
rs554679720 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SUMO3 | GRCh38.p7 | 21:44813794 | TTATAAAAGGCCATG[A/G]GGGACAAGCCCAGCC | 6612 |
rs554691700 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SUMO3 | GRCh38.p7 | 21:44814231 | AATTCTTAAAATTCT[C/T]CAGCAATTCAGAGTC | 6612 |
rs554730426 | snp | A/C/G | 0.000196736 | 0.00991628 | intron-variant | SUMO3 | GRCh38.p7 | 21:44808977 | AATTCTCAAATAAGC[A/C/G]TATCCCAAATGGCAG | 6612 |
rs554925406 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SUMO3 | GRCh38.p7 | 21:44813379 | CAGCGTTACCAAGAA[C/T]AACAGACACACACAC | 6612 |
rs555534981 | snp | C/G | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44809601 | TCCAAACTCATGTAC[C/G]TCTAAAATCCACCCT | 6612 |
rs555623325 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SUMO3 | GRCh38.p7 | 21:44816893 | TGGGCACACACTATA[A/G]GGGGCGTGATGGGGA | 6612 |
rs555677188 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB | SUMO3 | GRCh38.p7 | 21:44818942 | TGGAACGGACCTGAG[A/G]GCGGACACCCCTGCG | 6612 |
rs555801849 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | SUMO3 | GRCh38.p7 | 21:44815589 | CAGGCAGGATGGAAG[C/T]GGGGACCCCTGCATG | 6612 |
rs555908994 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SUMO3 | GRCh38.p7 | 21:44817445 | CCAGGCCCCTCAGAG[A/C]GCGCCCCTTGGGGGT | 6612 |
rs555973483 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SUMO3 | GRCh38.p7 | 21:44811197 | ACATGCACAAAGACA[C/T]GGACATACACACCAC | 6612 |
rs556849265 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | SUMO3 | GRCh38.p7 | 21:44819896 | ACAAAGGACACCGCT[G/T]GTGGACCGAACGCCA | 6612 |
rs556856827 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SUMO3 | GRCh38.p7 | 21:44815176 | TCCTTCCCTGGCTGG[C/G]AGAGGGACAACTGTC | 6612 |
rs556947907 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SUMO3 | GRCh38.p7 | 21:44812778 | CCCCCACATGTACAC[A/G]GCCCCACACGCCTGC | 6612 |
rs557082762 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | SUMO3 | GRCh38.p7 | 21:44806916 | CCATTCAACAGCAAT[G/T]CGAGGATGGACGGCC | 6612 |
rs557203917 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SUMO3 | GRCh38.p7 | 21:44814178 | ATGGGCAAGTCTTTA[C/G]GTAATTGTTGGCTTT | 6612 |
rs557203970 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SUMO3 | GRCh38.p7 | 21:44808329 | CATCCTGGCTAACAT[A/G]GTGAAACCCCGTCTC | 6612 |
rs557462998 | snp | A/G | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44812852 | ACACACAGTGGCCAC[A/G]AGCCCAGGCAGTACA | 6612 |
rs557753977 | snp | C/T | 0.000798403 | 0.0199641 | downstream-variant-500B | SUMO3 | GRCh38.p7 | 21:44805605 | AAATGCAGTGTTTAG[C/T]AGAAGCCAAGAGACA | 6612 |
rs557801169 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | SUMO3 | GRCh38.p7 | 21:44817642 | CTGCAGGAGCAGCAG[A/C]GCGGGGCCCGACACC | 6612 |
rs558279243 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | SUMO3 | GRCh38.p7 | 21:44815417 | GCACTCACCCCCCGA[A/C]TCCAGTCTTGGGCCA | 6612 |
rs558396587 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SUMO3 | GRCh38.p7 | 21:44816784 | GGGGAGACTAAAGCC[C/T]ACCCAAGGCTGGATA | 6612 |
rs558396629 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SUMO3 | GRCh38.p7 | 21:44810809 | CCTGCGTGAGAGCAG[C/T]CAGGGAAAGGCTCAC | 6612 |
rs558455681 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SUMO3 | GRCh38.p7 | 21:44810067 | AGGAGGGCAGCAGGA[A/G]GGAGAGCACGCAGCC | 6612 |
rs558531843 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SUMO3 | GRCh38.p7 | 21:44811133 | CCACATATACACACA[G/T]GCACACACCCACACA | 6612 |
rs558702606 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SUMO3 | GRCh38.p7 | 21:44808796 | GGTCCTTGCACCCCC[A/G]CTTCCCTTACAGTGA | 6612 |
rs558726447 | in-del | -/T | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44811580 | CTGTCTCAAAAAAAA[-/T]AAGTTGCTACTGAGA | 6612 |
rs558860123 | snp | G/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | SUMO3 | GRCh38.p7 | 21:44820076 | CAAGAAGACTCATGA[G/T]AAGGCAGGGAACTGG | 6612 |
rs559458202 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SUMO3 | GRCh38.p7 | 21:44810841 | GTGCAGCAGCCTAGA[A/G]AGGAGGGGAGGAGCG | 6612 |
rs559491120 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SUMO3 | GRCh38.p7 | 21:44817762 | GAGCTCGCGGCACAG[A/C]GCGCTTCGCGGGGGC | 6612 |
rs559698914 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SUMO3 | GRCh38.p7 | 21:44808230 | AAAAAAACTCTGTTT[C/T]GGCCGGGCGCGTTGG | 6612 |
rs559706416 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SUMO3 | GRCh38.p7 | 21:44811281 | TTCAGAAAACAATCA[A/G]TTGCTACTGAGGATG | 6612 |
rs559844751 | snp | C/G | 0.000399281 | 0.0141238 | downstream-variant-500B | SUMO3 | GRCh38.p7 | 21:44805279 | GAGAGATGTCCTAGA[C/G]TAACACCCAAGCTCA | 6612 |
rs559958203 | snp | C/G | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44817038 | GGAGGGGTGAGCACA[C/G]ACTGGGGGTGTGATG | 6612 |
rs560052222 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | SUMO3 | GRCh38.p7 | 21:44816493 | TGTCTGGCACTGAGC[C/G]TCCACCCTCATCTGT | 6612 |
rs560079719 | snp | A/G | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44815357 | CAAGGGGCCTTGGCA[A/G]TGAGGGGCTCCAGCT | 6612 |
rs560446341 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SUMO3 | GRCh38.p7 | 21:44815215 | GCCTAAATACAGGGA[A/G]TGGGATGTAGAAGGC | 6612 |
rs560883571 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SUMO3 | GRCh38.p7 | 21:44810244 | GAAAAAGGCACAAAC[A/G]GGAAGGACAAAGAAA | 6612 |
rs560906102 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SUMO3 | GRCh38.p7 | 21:44813551 | CACATGAGGGCAGTG[C/T]CTCTCCAGGGTCAGG | 6612 |
rs561026922 | snp | C/G | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44809747 | TGATGTGCCAGGGGA[C/G]GGGAAATGAGCCGCC | 6612 |
rs561272720 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | SUMO3 | GRCh38.p7 | 21:44819104 | AAGCGTCTGAGCCGT[A/T]TCTGTCCTGCCTGGG | 6612 |
rs561413613 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | SUMO3 | GRCh38.p7 | 21:44818636 | GGGCTGCCCCGGGCC[C/T]TCCACACCCGTCCTC | 6612 |
rs561690180 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | SUMO3 | GRCh38.p7 | 21:44806487 | TAACAGCAAGTGACA[C/G]TCTGTCCTCCCTACC | 6612 |
rs561700752 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SUMO3 | GRCh38.p7 | 21:44811442 | CCAGGCGTGGTGGCG[C/T]GTACCTGGAGTCCCA | 6612 |
rs561884767 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SUMO3 | GRCh38.p7 | 21:44817692 | GGGCGCGCGCCTTCC[A/C]AGCTGGGGAGGAGAC | 6612 |
rs561902815 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SUMO3 | GRCh38.p7 | 21:44815641 | CATGAGGATGCACTG[A/G]CTTCTTTAGGGAAGG | 6612 |
rs562045769 | in-del | -/C | 0.00119737 | 0.0244387 | intron-variant | SUMO3 | GRCh38.p7 | 21:44816724 | AATGCAGGGTGCATA[-/C]CCCAGGACTGAGACT | 6612 |
rs562119390 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SUMO3 | GRCh38.p7 | 21:44816190 | TGCTGAGAAAATTAA[C/T]ATCATATGTATTTTA | 6612 |
rs562883797 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SUMO3 | GRCh38.p7 | 21:44809154 | CCATTAGTCTCACTG[A/G]CAAGCCCTGGAAAGG | 6612 |
rs562942089 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SUMO3 | GRCh38.p7 | 21:44814546 | TCTCTTTTTTAAAAA[A/C]TTCTTATGAAACCAG | 6612 |
rs563141405 | snp | A/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | SUMO3 | GRCh38.p7 | 21:44819050 | GGGAGGCCGCACTTC[A/T]GGCTCAGCTGGGAAA | 6612 |
rs563261537 | snp | A/C | 0.00279162 | 0.0372561 | upstream-variant-2KB | SUMO3 | GRCh38.p7 | 21:44818610 | GGGCTCCTTTGGCCA[A/C]CGCTCCTACGGGGCT | 6612 |
rs563577210 | snp | C/T | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44810112 | GGGAATGGAGAAATG[C/T]GGTCAGGGGCAGAAA | 6612 |
rs563663928 | snp | A/G | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44811236 | ACACTCACGATTCAA[A/G]TTCTATGGGAAGTAA | 6612 |
rs564035339 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SUMO3 | GRCh38.p7 | 21:44817097 | GCGCACACCAGGGAC[G/T]CGATGATGGGGACGG | 6612 |
rs564074101 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SUMO3 | GRCh38.p7 | 21:44811411 | AGACCCCATCTCCAC[A/C]AAATAAAAAAATGAG | 6612 |
rs564173688 | snp | C/T | | | utr-variant-3-prime | SUMO3 | GRCh38.p7 | 21:44806210 | GAAAAAGGCCAATTT[C/T]GGTTGTGCCAATCCT | 6612 |
rs564291852 | snp | C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | SUMO3 | GRCh38.p7 | 21:44818611 | GGCTCCTTTGGCCAA[C/G]GCTCCTACGGGGCTG | 6612 |
rs564506954 | snp | A/G | | | downstream-variant-500B | SUMO3, LINC01424 | GRCh38.p7 | 21:44805186 | TAAAGCCAAATCAAT[A/G]TCAGTTCAGTTTCAA | 6612 |
rs564592934 | in-del | -/AC | 0.0023933 | 0.0345097 | intron-variant | SUMO3 | GRCh38.p7 | 21:44816245 | AAGCCACCTACAAAA[-/AC]ATAAAGGACATTTAT | 6612 |
rs564735586 | snp | C/T | 0.000265388 | 0.0115162 | intron-variant | SUMO3 | GRCh38.p7 | 21:44809030 | CGCCCTGGAACCACG[C/T]GAAGCCAGCTCCGTA | 6612 |
rs564872507 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SUMO3 | GRCh38.p7 | 21:44808468 | CACAGTGAGCTGAGA[C/T]TGCGCCACTGCATTC | 6612 |
rs565094796 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | SUMO3 | GRCh38.p7 | 21:44819146 | CAACTGAGCAACGTC[A/G]CAAAGCCATGGAGAC | 6612 |
rs565232024 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | SUMO3 | GRCh38.p7 | 21:44819562 | AGACACACTAAACTC[C/T]GGCAGGCTGTGGATG | 6612 |
rs565636465 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | SUMO3 | GRCh38.p7 | 21:44817273 | GGGGCGCGATGGGTG[G/T]GAGTAGGTGCACACT | 6612 |
rs565800520 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | SUMO3 | GRCh38.p7 | 21:44805508 | TTCCAGCGGCTAGCT[C/T]TTCAATCAAAGTTTC | 6612 |
rs566015193 | snp | A/G | | | utr-variant-3-prime | SUMO3 | GRCh38.p7 | 21:44806092 | CTTACTTTTTTATGT[A/G]TAGACCATAATCATT | 6612 |
rs566166261 | in-del | -/ACAC | 0.00159617 | 0.0282053 | intron-variant | SUMO3 | GRCh38.p7 | 21:44811064 | CACACACCCACACAT[-/ACAC]ACACACGAATGCACA | 6612 |
rs566292662 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SUMO3 | GRCh38.p7 | 21:44815414 | GCGGCACTCACCCCC[C/T]GACTCCAGTCTTGGG | 6612 |
rs566395455 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SUMO3 | GRCh38.p7 | 21:44816781 | ATGGGGGAGACTAAA[A/G]CCCACCCAAGGCTGG | 6612 |
rs566790078 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SUMO3 | GRCh38.p7 | 21:44810565 | ACAGGCCCACGAAAG[C/T]GCGTGCCCTCAACAC | 6612 |
rs566816351 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SUMO3 | GRCh38.p7 | 21:44813804 | CCATGGGGGACAAGC[A/C]CAGCCTGGACTAATT | 6612 |
rs566832544 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | SUMO3 | GRCh38.p7 | 21:44819696 | TGTCACGAAGTGATG[C/T]GTGACTACAGTCATG | 6612 |
rs566847807 | snp | C/T | 0.000798403 | 0.0199641 | missense | SUMO3 | GRCh38.p7 | 21:44814050 | ACTGCACCACGGAGC[C/T]GTCCTGCCCGGCCAC | 6612 |
rs566886960 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SUMO3 | GRCh38.p7 | 21:44808774 | GAGTGGGAAGGGGCC[A/G]CTGAGTGGTCCTTGC | 6612 |
rs566952879 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SUMO3 | GRCh38.p7 | 21:44808272 | AATCCCAGCACTTTG[A/G]GGGGCTGAGGTGGGC | 6612 |
rs567416200 | snp | A/C | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44808755 | CAGCAAGCGTCCAGA[A/C]AATGAGTGGGAAGGG | 6612 |
rs567807837 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime | SUMO3 | GRCh38.p7 | 21:44818126 | GCACGGGGGTCACGT[A/G]GCTGCGCGCGTTCAC | 6612 |
rs567911760 | snp | A/G | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44813715 | AGAACACAGCACCCC[A/G]GGCAGCCGCCCTGTC | 6612 |
rs567917007 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | SUMO3 | GRCh38.p7 | 21:44815981 | TCTTTCCAGCACCAC[C/T]GGGCCCCAGAGTCCA | 6612 |
rs567919816 | snp | A/C | 0.000399281 | 0.0141238 | downstream-variant-500B | SUMO3 | GRCh38.p7 | 21:44805499 | ATACTAACCTTCCAG[A/C]GGCTAGCTTTTCAAT | 6612 |
rs567946117 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SUMO3 | GRCh38.p7 | 21:44812654 | CCCAAGTTTCTAGAA[G/T]GATTTGAACAGGAGG | 6612 |
rs567993612 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | SUMO3 | GRCh38.p7 | 21:44806857 | GTGGTGAATGTCCTC[A/G]AGTTTCCGCAGACAC | 6612 |
rs568054362 | in-del | -/G | 0.00159617 | 0.0282053 | intron-variant | SUMO3 | GRCh38.p7 | 21:44817193 | GCGTGGGCGTACACC[-/G]GGGGGGCGCGATGGG | 6612 |
rs568054405 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SUMO3 | GRCh38.p7 | 21:44810672 | CTGTAGCATCTGGGC[A/G]CCTCCAGAACCTGCA | 6612 |
rs568175970 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SUMO3 | GRCh38.p7 | 21:44810966 | CACACCCACACATGC[A/C]CACCCATGCACACAC | 6612 |
rs568371060 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | SUMO3 | GRCh38.p7 | 21:44809654 | TGAGGAAGCGTAACA[C/T]GTCACAGTGACGCTA | 6612 |
rs569035186 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SUMO3 | GRCh38.p7 | 21:44813735 | GCCGCCCTGTCAGGA[A/G]GAAAAACCCACCACA | 6612 |
rs569108454 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SUMO3 | GRCh38.p7 | 21:44808580 | TGCCCTGCAACGTGA[C/T]AGATGAAATCTCATT | 6612 |
rs569153183 | in-del | -/G | 0.00199481 | 0.0315187 | intron-variant | SUMO3 | GRCh38.p7 | 21:44816768 | CCCCAGCATGGCAAT[-/G]GGGGAGACTAAAGCC | 6612 |
rs569182640 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | SUMO3 | GRCh38.p7 | 21:44818855 | CAGGACGGCCTCCCC[A/G]GACTTGCGGGCGCCA | 6612 |
rs569206700 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SUMO3 | GRCh38.p7 | 21:44809367 | CACGCGGTGCCTGAC[A/G]CCACTGCTTTCAGAA | 6612 |
rs569245012 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | SUMO3 | GRCh38.p7 | 21:44819238 | AGAGCCCCCACTTAG[A/G]AGGGGGAAGGCTGCT | 6612 |
rs569413045 | snp | A/G | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44815775 | GGGCAGGGCAGGGCC[A/G]GCCACAGTGCCTCTG | 6612 |
rs569672376 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | SUMO3 | GRCh38.p7 | 21:44806774 | TGGCCCAATTTAAGT[G/T]ACAGATTCATCCCTG | 6612 |
rs569958983 | snp | C/T | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44815112 | CATGCTGAGCTGCTG[C/T]CCTCAGGAAGCACTG | 6612 |
rs570057260 | snp | C/T | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44810825 | CAGGGAAAGGCTCAC[C/T]GTGCAGCAGCCTAGA | 6612 |
rs570112189 | in-del | -/CACATACACA | 0.00597247 | 0.0543191 | intron-variant | SUMO3 | GRCh38.p7 | 21:44811095 | ACACATGCACACACC[-/CACATACACA]CACATGCACACACCC | 6612 |
rs570204425 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SUMO3 | GRCh38.p7 | 21:44815435 | CAGTCTTGGGCCAGA[C/T]ACCCCTGCCCACTCC | 6612 |
rs570241787 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SUMO3 | GRCh38.p7 | 21:44815853 | TAAGCAAGTGAACTC[G/T]TGAGTTAAAAAGTGA | 6612 |
rs570277890 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SUMO3 | GRCh38.p7 | 21:44810619 | TCCAGATGCGCCTCC[A/G]GGAGGCTGGCCGGAG | 6612 |
rs570281705 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime | SUMO3 | GRCh38.p7 | 21:44818033 | GGGCGAGTCACGCTC[C/T]CGGCCCCGCCGCTCT | 6612 |
rs570388538 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SUMO3 | GRCh38.p7 | 21:44811629 | AACAGAAAGAAAAAA[G/T]AACTTTTGGAAATTA | 6612 |
rs570411381 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SUMO3 | GRCh38.p7 | 21:44810900 | GAGAACACTCCCAAC[A/G]CAGGCACACACATGC | 6612 |
rs570492929 | in-del | -/C | 0.000798403 | 0.0199641 | intron-variant | SUMO3 | GRCh38.p7 | 21:44817083 | ATAGGGAGGGGTGGG[-/C]GCACACCAGGGACGC | 6612 |
rs570820514 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SUMO3 | GRCh38.p7 | 21:44814898 | TGTTGCCTGAAAATG[A/C]ATTTTGAGTTGAGGC | 6612 |
rs570996813 | snp | A/G | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44812214 | GGCTTGCACCACCAC[A/G]CCTGGCTAATTTTTT | 6612 |
rs571390503 | snp | C/G/T | 0.00159617 | 0.0282053 | upstream-variant-2KB | SUMO3 | GRCh38.p7 | 21:44818336 | CCCCGCGTCGCCCGG[C/G/T]CCCCGACTCCTTTCC | 6612 |
rs571426956 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | SUMO3 | GRCh38.p7 | 21:44818706 | GGAGGTCAAACCACC[C/T]CCAGGTCAGCGCTGG | 6612 |
rs571587348 | snp | A/G | 6.63174e-05 | 0.00575798 | intron-variant | SUMO3 | GRCh38.p7 | 21:44814154 | TGTCTCAAAATAACC[A/G]CGACTTGAATGGGCA | 6612 |
rs571908927 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SUMO3 | GRCh38.p7 | 21:44807224 | GAGGCATTGCTGTAT[A/G]CTCACTACAGCCCTT | 6612 |
rs572025056 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SUMO3 | GRCh38.p7 | 21:44816955 | GGGAGGGGTGGACGC[A/C]CACTGGGGGTGTGAT | 6612 |
rs572235275 | snp | A/G | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44808818 | TTACAGTGAGGACGG[A/G]CCCAGCACTTGGCTC | 6612 |
rs572548390 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | SUMO3 | GRCh38.p7 | 21:44820038 | CCCCTCCGGAGGGTC[A/G]CCACACCTGGCGATG | 6612 |
rs572689217 | snp | C/T | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44811536 | ATGATCACACCACTG[C/T]GCTCCAGCTTGGGGG | 6612 |
rs572723034 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SUMO3 | GRCh38.p7 | 21:44810742 | AGCACAGCCATCCAT[A/G]TACACAGCTTTTCAG | 6612 |
rs572723951 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SUMO3 | GRCh38.p7 | 21:44815520 | TCCCCATCCCGAATG[C/T]GGCCTCCAGCACAGA | 6612 |
rs573244358 | in-del | -/GGGCTGGGGG | 0.341909 | 0.232492 | intron-variant | SUMO3 | GRCh38.p7 | 21:44817890 | GGTGGGGGCGGAGCC[-/GGGCTGGGGG]CGGGACGCCCGCGAT | 6612 |
rs573396939 | snp | A/T | 0.00874735 | 0.0655527 | intron-variant | SUMO3 | GRCh38.p7 | 21:44812999 | CTCACCTTTCGCAGG[A/T]GAAAATAAGATCTGC | 6612 |
rs573860766 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SUMO3 | GRCh38.p7 | 21:44812836 | GCACCCGGGAAGTCA[A/C]ACACACAGTGGCCAC | 6612 |
rs573872479 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SUMO3 | GRCh38.p7 | 21:44813400 | ACACACACACACCAC[A/G]TCACAAACAGCAGCC | 6612 |
rs573930854 | snp | C/T | 0.00279162 | 0.0372561 | upstream-variant-2KB | SUMO3 | GRCh38.p7 | 21:44818563 | GCGCCACCCGCCTCC[C/T]TGCCGCCGCGGTTTC | 6612 |
rs574101160 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SUMO3 | GRCh38.p7 | 21:44811199 | ATGCACAAAGACACG[A/G]ACATACACACCACAC | 6612 |
rs574110764 | snp | A/C | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44809633 | TCTTTACATACGAAA[A/C]CCAGGTGAGGAAGCG | 6612 |
rs574171369 | in-del | -/CATGCACACACCCATGCACACACCCACA | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44810971 | CCACACATGCACACC[-/CATGCACACACCCATGCACACACCCACA]CATGCACACACCCAC | 6612 |
rs574228309 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SUMO3 | GRCh38.p7 | 21:44816921 | GGAGGGGTGGGCGCA[A/C]ATCGTGGAGGGGGTG | 6612 |
rs574244469 | snp | A/G | 0.00279162 | 0.0372561 | downstream-variant-500B | SUMO3 | GRCh38.p7 | 21:44805222 | ATAGGTAAGTTGTCC[A/G]TGGCAGAAGGAAAGC | 6612 |
rs575194657 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SUMO3 | GRCh38.p7 | 21:44812801 | ACGCCTGCCATCCCG[C/T]AGCGCAGAGGAGAAC | 6612 |
rs575227935 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | SUMO3 | GRCh38.p7 | 21:44819428 | CCCTTCCGAGGGGAC[A/G]TGGCGCCTCAGAGCC | 6612 |
rs575363947 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SUMO3 | GRCh38.p7 | 21:44807418 | CTGAGTCCTAGGACC[C/T]ACAGGAGCCTTGCGC | 6612 |
rs575385144 | in-del | -/T | 0.322959 | 0.239117 | intron-variant | SUMO3 | GRCh38.p7 | 21:44817871 | GGACGCGGGGCGGAG[-/T]CGGGGTGGGGGCGGA | 6612 |
rs575463686 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SUMO3 | GRCh38.p7 | 21:44808330 | ATCCTGGCTAACATG[A/G]TGAAACCCCGTCTCT | 6612 |
rs575492672 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SUMO3 | GRCh38.p7 | 21:44816069 | GGGACCCACCAGAAG[C/T]GGGGCCTGTGAGGTG | 6612 |
rs575949477 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SUMO3 | GRCh38.p7 | 21:44812142 | GCTCCCTGCAGCCTC[C/T]ACCTCCTGGGCTCAA | 6612 |
rs576246097 | snp | C/G | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44807690 | GCAAGGCTGGAAGTA[C/G]TCATGCTCCCAGATG | 6612 |
rs576272867 | snp | G/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | SUMO3 | GRCh38.p7 | 21:44818444 | GGGAGGACGCTGGGG[G/T]TGACGTTCCCTCTCA | 6612 |
rs576518803 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SUMO3 | GRCh38.p7 | 21:44809453 | GGTTTTGTTACACCA[C/T]TGCATACTGGGAACT | 6612 |
rs576532928 | snp | C/T | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44814393 | AAATAAGAGAAAATC[C/T]ATCTTTATTTTAAAG | 6612 |
rs576623416 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SUMO3 | GRCh38.p7 | 21:44816164 | CACATGGCAGAGCTA[A/G]GTGTAAATACTGCTG | 6612 |
rs577448877 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | SUMO3 | GRCh38.p7 | 21:44820091 | GAAGGCAGGGAACTG[G/T]CAAATGAGTAACAGC | 6612 |
rs577700723 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SUMO3 | GRCh38.p7 | 21:44811915 | CCCATAAAGTGCCCA[G/T]CAGCATGAGTGAGAA | 6612 |
rs577737201 | snp | C/G/T | 0.00119737 | 0.0244387 | intron-variant | SUMO3 | GRCh38.p7 | 21:44812767 | GGGCAGAGCCCCCCC[C/G/T]ACATGTACACGGCCC | 6612 |
rs577791448 | snp | C/T | 0.00159617 | 0.0282053 | upstream-variant-2KB | SUMO3 | GRCh38.p7 | 21:44819587 | TGGATGACGGCAGCC[C/T]GCTTCAGTGTTGTGG | 6612 |
rs577792423 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | SUMO3 | GRCh38.p7 | 21:44818573 | CCTCCCTGCCGCCGC[C/G]GTTTCCTGTCAGCCC | 6612 |
rs577829253 | snp | C/G | 0.00119737 | 0.0244387 | upstream-variant-2KB | SUMO3 | GRCh38.p7 | 21:44819019 | CTCATCTGATGGTGA[C/G]CCCGGCCGAAGGCGG | 6612 |
rs577859215 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SUMO3 | GRCh38.p7 | 21:44807632 | TGATCTTCTTCCATC[C/G]TCTAAGCAAGAGGAA | 6612 |
rs577864011 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SUMO3 | GRCh38.p7 | 21:44813446 | AGCTGGGCACTGCCA[C/G]TGGGGCAGCTCATTA | 6612 |
rs577991934 | snp | A/G | 0.000104462 | 0.00722633 | missense, intron-variant | SUMO3 | GRCh38.p7 | 21:44813896 | GTCCAGCCCCGAGAC[A/G]CTCGTGCTCTGGGGA | 6612 |
rs578065725 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | SUMO3 | GRCh38.p7 | 21:44806246 | GTGTACCAACGCCAG[A/G]TACTGAGCAGGGAGT | 6612 |
rs745315383 | snp | A/G | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44809913 | CTTTCCAGAAGCCGA[A/G]TAGAACTTCTACAAT | 6612 |
rs745388080 | in-del | -/A | 0.222676 | 0.248502 | intron-variant | SUMO3 | GRCh38.p7 | 21:44808515 | GCGAGACTCCGTCTC[-/A]AAAAAAAAAGTCTGT | 6612 |
rs745475927 | snp | A/G | 9.13534e-05 | 0.00675784 | intron-variant | SUMO3 | GRCh38.p7 | 21:44813837 | ACAGCACAAGCCCCC[A/G]CCTGCCCATCCACGA | 6612 |
rs745539728 | snp | C/T | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44809361 | CTCTTTCACGCGGTG[C/T]CTGACACCACTGCTT | 6612 |
rs745655859 | snp | G/T | 0.000141263 | 0.00840306 | utr-variant-5-prime | SUMO3 | GRCh38.p7 | 21:44818019 | AAGCAGCGCGGAGCG[G/T]GCGAGTCACGCTCTC | 6612 |
rs745707690 | snp | C/T | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44807930 | CTGCCACTGCCTCAG[C/T]GGTGTGTAGGTTTCC | 6612 |
rs745718998 | snp | A/G | | | upstream-variant-2KB | SUMO3 | GRCh38.p7 | 21:44819507 | AGTTATCGACTCCAA[A/G]ACACCGTTAATCATA | 6612 |
rs745948436 | snp | A/T | 0.00011914 | 0.00771723 | intron-variant | SUMO3 | GRCh38.p7 | 21:44808389 | GTGGTGGTGGGCACC[A/T]ATAGTCCCAGCTACT | 6612 |
rs745991153 | snp | A/G | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44811018 | CACACACCCACATAT[A/G]CACACACGCACACAC | 6612 |
rs746082399 | snp | C/T | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44807420 | GAGTCCTAGGACCCA[C/T]AGGAGCCTTGCGCTT | 6612 |
rs746124313 | in-del | -/TG | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44811016 | GCACACACCCACATA[-/TG]TGCACACACGCACAC | 6612 |
rs746177399 | snp | A/G | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44814757 | ATCAGCAAATGTGAG[A/G]GAAGCCACCTCCGAG | 6612 |
rs746284587 | snp | C/G | | | utr-variant-3-prime | SUMO3 | GRCh38.p7 | 21:44806675 | AAAAATGTTGTAGGA[C/G]GGGGGGAAAACACAA | 6612 |
rs746769198 | snp | A/C/G | 4.98661e-05 | 0.00499309 | synonymous-codon, intron-variant | SUMO3 | GRCh38.p7 | 21:44813970 | CGGGGGAGCAAGGTG[A/C/G]CGCACCTGCCTCTCG | 6612 |
rs746948611 | snp | A/G | | | upstream-variant-2KB | SUMO3 | GRCh38.p7 | 21:44819536 | TAAAACAACACGACC[A/G]TAGGTAGCACAGACA | 6612 |
rs747315535 | in-del | -/C | | | downstream-variant-500B | SUMO3 | GRCh38.p7 | 21:44805529 | CAAAGTTTCTCAGTG[-/C]CAGTGGCTGCCTGGA | 6612 |
rs747380882 | snp | C/G/T | 6.47387e-05 | 0.0056891 | synonymous-codon, intron-variant | SUMO3 | GRCh38.p7 | 21:44813895 | GGTCCAGCCCCGAGA[C/G/T]GCTCGTGCTCTGGGG | 6612 |
rs747431914 | snp | A/G | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44808274 | TCCCAGCACTTTGGG[A/G]GGCTGAGGTGGGCAG | 6612 |
rs747553513 | snp | A/T | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44816175 | GCTAAGTGTAAATAC[A/T]GCTGAGAAAATTAAT | 6612 |
rs747725284 | snp | A/C | 1.66396e-05 | 0.00288436 | missense, intron-variant | SUMO3 | GRCh38.p7 | 21:44813965 | CTCTGCGGGGGAGCA[A/C]GGTGCCGCACCTGCC | 6612 |
rs747869345 | snp | G/T | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44810859 | GAGGGGAGGAGCGCA[G/T]AGGAGAACGGACAGG | 6612 |
rs748103023 | snp | A/G | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44810119 | GAGAAATGTGGTCAG[A/G]GGCAGAAACATTTCC | 6612 |
rs748400256 | snp | A/G | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44813119 | ATCCAAAGTGGGAGG[A/G]AAAGAGGAGGAAATC | 6612 |
rs748453958 | in-del | -/A | | | utr-variant-3-prime | SUMO3 | GRCh38.p7 | 21:44806624 | ATCCCTGGCCAGACT[-/A]AAAAGCGAACATTCA | 6612 |
rs748686313 | snp | G/T | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44815807 | TCCAAACAGAATGAC[G/T]ATCTGTCCCAGACCC | 6612 |
rs748729056 | snp | C/T | 3.69781e-05 | 0.00429973 | missense, intron-variant | SUMO3 | GRCh38.p7 | 21:44813906 | GAGACGCTCGTGCTC[C/T]GGGGATGCCTGGAAC | 6612 |
rs748750111 | snp | A/G | | | upstream-variant-2KB | SUMO3 | GRCh38.p7 | 21:44819420 | CAACCAGCCCCTTCC[A/G]AGGGGACGTGGCGCC | 6612 |
rs749547339 | snp | A/G | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44814691 | CGGGAATCCAACTGA[A/G]GACGGCCACTCCCCA | 6612 |
rs749651427 | snp | C/G | 0.000343466 | 0.0131002 | intron-variant | SUMO3 | GRCh38.p7 | 21:44808487 | GCCACTGCATTCTAG[C/G]CTGGGCAACAAAGCG | 6612 |
rs749657761 | snp | A/G | 1.65143e-05 | 0.00287348 | synonymous-codon | SUMO3 | GRCh38.p7 | 21:44814045 | CTTGAACTGCACCAC[A/G]GAGCCGTCCTGCCCG | 6612 |
rs749706803 | snp | C/T | 1.67826e-05 | 0.00289673 | intron-variant | SUMO3 | GRCh38.p7 | 21:44809020 | AATCGGAAGTCGCCC[C/T]GGAACCACGCGAAGC | 6612 |
rs749856925 | in-del | -/G | 1.65312e-05 | 0.00287495 | intron-variant | SUMO3 | GRCh38.p7 | 21:44814126 | AAGACACCAGAGACT[-/G]GCCTCAAAACTGTGT | 6612 |
rs750010874 | snp | A/T | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44810616 | CCCTCCAGATGCGCC[A/T]CCAGGAGGCTGGCCG | 6612 |
rs750140987 | snp | C/G | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44814528 | CAACAGAGCAAGACC[C/G]CATCTCTTTTTTAAA | 6612 |
rs750254252 | snp | A/G/T | 0.000756223 | 0.0194321 | synonymous-codon, intron-variant | SUMO3 | GRCh38.p7 | 21:44813865 | CGAAGAGGGCACCTC[A/G/T]GGCAGCTGCATCTGG | 6612 |
rs750460210 | snp | A/T | | | upstream-variant-2KB | SUMO3 | GRCh38.p7 | 21:44819112 | GAGCCGTTTCTGTCC[A/T]GCCTGGGAAAGGCTC | 6612 |
rs750619125 | snp | A/G | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44816823 | TGGGCGCGCATGGTG[A/G]GGGAGGCGCAATGCA | 6612 |
rs750627818 | in-del | -/AT | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44811062 | CGCACACACCCACAC[-/AT]ACACACACACGAATG | 6612 |
rs750770742 | snp | A/G | 3.30688e-05 | 0.00406612 | missense | SUMO3 | GRCh38.p7 | 21:44814013 | ATCAGCTTGCTCAGC[A/G]GCGTGTGCCTCTTGA | 6612 |
rs750782626 | snp | G/T | 1.65348e-05 | 0.00287526 | intron-variant | SUMO3 | GRCh38.p7 | 21:44814127 | AGACACCAGAGACTG[G/T]CCTCAAAACTGTGTC | 6612 |
rs751117587 | snp | A/G | 8.52806e-05 | 0.0065294 | intron-variant | SUMO3 | GRCh38.p7 | 21:44817937 | CGTGCAGGCGGGGTC[A/G]CCGCGCTTACCTTGG | 6612 |
rs751268344 | snp | A/G | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44809208 | CTGACAAGCCCTGGA[A/G]AGGAAAAGCAGTGGC | 6612 |
rs751299212 | snp | C/G/T | 2.7541e-05 | 0.00371076 | utr-variant-3-prime | SUMO3 | GRCh38.p7 | 21:44806856 | CGTGGTGAATGTCCT[C/G/T]GAGTTTCCGCAGACA | 6612 |
rs751308919 | snp | C/T | 1.64789e-05 | 0.0028704 | missense | SUMO3 | GRCh38.p7 | 21:44809070 | GAGTGTCAGTTTCAT[C/T]GATTGGCTGCCCGTC | 6612 |
rs751362750 | snp | A/G | 0.000349333 | 0.0132115 | synonymous-codon | SUMO3 | GRCh38.p7 | 21:44807014 | CTGCTGGAACACGTC[A/G]ATGGTGTCCTCGTCC | 6612 |
rs751507879 | snp | C/T | | | utr-variant-3-prime | SUMO3 | GRCh38.p7 | 21:44806286 | GGGGTGGCAGGGGGG[C/T]GGGTCCTGGGCCTCA | 6612 |
rs751745951 | snp | A/G | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44808729 | GCCCCTAAGCTGCAC[A/G]CGGGCTACAACAGCA | 6612 |
rs752104087 | snp | A/T | 1.65474e-05 | 0.00287636 | missense | SUMO3 | GRCh38.p7 | 21:44813999 | CGCAGTAGGCCTTCA[A/T]CAGCTTGCTCAGCGG | 6612 |
rs752250709 | snp | A/G | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44807178 | CCTTGGCTCTTGTCC[A/G]TCCCCTCACTGCAGC | 6612 |
rs752324891 | snp | A/C | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44812817 | AGCGCAGAGGAGAAC[A/C]TGGGCACCCGGGAAG | 6612 |
rs752356084 | snp | C/T | 1.65781e-05 | 0.00287902 | intron-variant | SUMO3 | GRCh38.p7 | 21:44814152 | TGTGTCTCAAAATAA[C/T]CGCGACTTGAATGGG | 6612 |
rs752594939 | in-del | -/AATGGCTGCAGCCCCGGGGGG | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44815713 | CGTCCCCCACAGGGT[-/AATGGCTGCAGCCCCGGGGGG]AATGGCTGCAGCCCC | 6612 |
rs752652207 | snp | A/G | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44808239 | CTGTTTCGGCCGGGC[A/G]CGTTGGCTCATGCCT | 6612 |
rs752657903 | in-del | -/ACAC | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44811204 | CAAAGACACGGACAT[-/ACAC]ACCACACACACCTAC | 6612 |
rs752881136 | snp | A/C/T | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44814604 | GCTATACAGCACTAG[A/C/T]AAAAGAAACCAAAAA | 6612 |
rs752921902 | in-del | -/CA | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44813387 | CAAGAACAACAGACA[-/CA]CACACACACCACGTC | 6612 |
rs753041683 | snp | C/T | | | upstream-variant-2KB | SUMO3 | GRCh38.p7 | 21:44819903 | ACACCGCTGGTGGAC[C/T]GAACGCCAAGAGGTT | 6612 |
rs753051748 | snp | C/T | | | upstream-variant-2KB | SUMO3 | GRCh38.p7 | 21:44819789 | TGGTCTGAATTCAAT[C/T]CATGCTGTGTCTGTC | 6612 |
rs753166634 | snp | G/T | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44809786 | ACTAACCTTCCAGTG[G/T]CTAGCTTTTCAATCA | 6612 |
rs753180269 | in-del | -/CACACCCATGCA | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44810965 | ACACACCCACACATG[-/CACACCCATGCA]CACACCCATGCACAC | 6612 |
rs753207170 | snp | C/T | 8.10734e-05 | 0.00636633 | missense, intron-variant | SUMO3 | GRCh38.p7 | 21:44813887 | TGCATCTGGGTCCAG[C/T]CCCGAGACGCTCGTG | 6612 |
rs753293896 | snp | A/G | | | utr-variant-3-prime | SUMO3 | GRCh38.p7 | 21:44805961 | TATTTGGAAAGCAGC[A/G]CGGCACAAACCCACG | 6612 |
rs753469528 | snp | C/G/T | | | upstream-variant-2KB | SUMO3 | GRCh38.p7 | 21:44819990 | AACCGTGGCCTACCA[C/G/T]GAGCACAGGGTAAAG | 6612 |
rs753636634 | snp | A/G | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44813665 | CCCCAAGAGCCTTCA[A/G]CATCACAGACTTCAC | 6612 |
rs753782808 | in-del | -/AT | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44808919 | AAAATAAATAATCTA[-/AT]AATCAATATCATTAA | 6612 |
rs753846440 | snp | A/C/G | 6.66539e-05 | 0.00577264 | missense, intron-variant | SUMO3 | GRCh38.p7 | 21:44813877 | CTCGGGCAGCTGCAT[A/C/G]TGGGTCCAGCCCCGA | 6612 |
rs754002542 | in-del | -/GAA | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44813733 | CAGCCGCCCTGTCAG[-/GAA]GAAAAACCCACCACA | 6612 |
rs754192551 | snp | C/T | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44810585 | GCCCTCAACACTGTG[C/T]GCCAAGTCCCCTCTC | 6612 |
rs754278810 | snp | C/T | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44809860 | ACTGAATCTTCTCTG[C/T]CCTGGTGCCCTGACC | 6612 |
rs754612226 | snp | A/G | 0.000183292 | 0.00957144 | missense, intron-variant | SUMO3 | GRCh38.p7 | 21:44813957 | CGGGGAGGCTCTGCG[A/G]GGGAGCAAGGTGCCG | 6612 |
rs754917215 | snp | C/T | | | utr-variant-3-prime | SUMO3 | GRCh38.p7 | 21:44806360 | CAAATTACCAAAAGA[C/T]TCGGTTATTTTTTAA | 6612 |
rs755035490 | snp | A/G | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44809798 | GTGGCTAGCTTTTCA[A/G]TCAAAGTTTCTCAGT | 6612 |
rs755058031 | in-del | -/ACAC | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44811176 | CACACACCCACACAT[-/ACAC]ACACATGCACAAAGA | 6612 |
rs755259159 | snp | C/G | | | upstream-variant-2KB | SUMO3 | GRCh38.p7 | 21:44819669 | TACCGCTCGAAATTA[C/G]GCCAGTTGCTGTGTC | 6612 |
rs755293698 | snp | A/G | | | upstream-variant-2KB | SUMO3 | GRCh38.p7 | 21:44819301 | CCCCAGTCCCAGGCA[A/G]GTCATAAGGTGTGGT | 6612 |
rs755381339 | snp | C/G | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44808761 | GCGTCCAGACAATGA[C/G]TGGGAAGGGGCCGCT | 6612 |
rs755432737 | snp | A/G | 1.64781e-05 | 0.00287033 | intron-variant | SUMO3 | GRCh38.p7 | 21:44809122 | CATTGACAAGCCCTG[A/G]AAAGGAAAAGCAGTG | 6612 |
rs755522545 | snp | A/G | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44817410 | GCGCCCTGGAAGGAC[A/G]GCAGTGCTGCTCACA | 6612 |
rs755639488 | snp | A/G | 0.000101003 | 0.00710573 | utr-variant-3-prime | SUMO3 | GRCh38.p7 | 21:44806933 | GAGGATGGACGGCCC[A/G]GGCTGGGGACGGGCC | 6612 |
rs755714051 | snp | C/T | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44812818 | GCGCAGAGGAGAACA[C/T]GGGCACCCGGGAAGT | 6612 |
rs755873719 | snp | G/T | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44811953 | CACCTCTGAGGCACA[G/T]AAGGAAACACTGAAT | 6612 |
rs755885948 | in-del | -/CTTTTTT/TT/TTT | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44812053 | ACTGAACTTCTCACC[-/CTTTTTT/TT/TTT]TTTTTTTTTTTTTTT | 6612 |
rs756017236 | snp | C/T | 1.64822e-05 | 0.00287068 | utr-variant-3-prime | SUMO3 | GRCh38.p7 | 21:44806870 | TCGAGTTTCCGCAGA[C/T]ACCTTTGTGGTCGGC | 6612 |
rs756147512 | snp | C/T | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44813534 | AATGGAAAACCACAC[C/T]GCACATGAGGGCAGT | 6612 |
rs756313811 | snp | A/G | 1.76157e-05 | 0.00296775 | intron-variant | SUMO3 | GRCh38.p7 | 21:44809009 | TACCCCGCACAAATC[A/G]GAAGTCGCCCTGGAA | 6612 |
rs756435148 | snp | C/T | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44809838 | GTGTGGAATGGTCAA[C/T]TCAAACACTGAATCT | 6612 |
rs756592870 | snp | C/T | | | upstream-variant-2KB | SUMO3 | GRCh38.p7 | 21:44819952 | AGGGGATCGAATGGA[C/T]GGAGGAACCAGAGCT | 6612 |
rs756674057 | snp | A/G | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44817668 | ACACCGGGCGCTCAA[A/G]GAGGCGCTGGGCGCG | 6612 |
rs757031405 | snp | A/G | | | upstream-variant-2KB | SUMO3 | GRCh38.p7 | 21:44819433 | CCGAGGGGACGTGGC[A/G]CCTCAGAGCCCACAG | 6612 |
rs757215172 | snp | A/C | 4.02212e-05 | 0.0044843 | intron-variant | SUMO3 | GRCh38.p7 | 21:44817941 | CAGGCGGGGTCGCCG[A/C]GCTTACCTTGGGCTT | 6612 |
rs757331290 | snp | C/T | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44808240 | TGTTTCGGCCGGGCG[C/T]GTTGGCTCATGCCTT | 6612 |
rs757355739 | snp | A/C | 1.86173e-05 | 0.00305095 | intron-variant | SUMO3 | GRCh38.p7 | 21:44809002 | TGGCAGTTACCCCGC[A/C]CAAATCGGAAGTCGC | 6612 |
rs757524153 | snp | C/T | 0.00579705 | 0.053525 | intron-variant | SUMO3 | GRCh38.p7 | 21:44808369 | TACAAAAAAATTAGC[C/T]GGGAGTGGTGGTGGG | 6612 |
rs757971771 | snp | C/T | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44811566 | GACAGAGTGAGACCC[C/T]GTCTCAAAAAAAATA | 6612 |
rs757976987 | snp | C/T | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44810690 | TCCAGAACCTGCAAT[C/T]CAGACAGATCACCCC | 6612 |
rs758021811 | snp | C/T | 4.957e-05 | 0.00497821 | synonymous-codon | SUMO3 | GRCh38.p7 | 21:44814024 | CAGCGGCGTGTGCCT[C/T]TTGATCTTGAACTGC | 6612 |
rs758026942 | snp | C/T | | | upstream-variant-2KB | SUMO3 | GRCh38.p7 | 21:44820049 | GGTCGCCACACCTGG[C/T]GATGGTCCCAACAAG | 6612 |
rs758194833 | snp | C/T | | | utr-variant-3-prime | SUMO3 | GRCh38.p7 | 21:44806091 | TCTTACTTTTTTATG[C/T]ATAGACCATAATCAT | 6612 |
rs758272073 | snp | A/G | | | downstream-variant-500B | SUMO3 | GRCh38.p7 | 21:44805271 | CAGAAAACGAGAGAT[A/G]TCCTAGACTAACACC | 6612 |
rs758414861 | snp | C/T | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44814575 | AGTAAAAACACATAT[C/T]CAAAAGTCATGCAGC | 6612 |
rs758563955 | snp | A/G | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44816838 | GGGGAGGCGCAATGC[A/G]GAGAAGTGGGCGCAC | 6612 |
rs758598812 | snp | C/G | | | upstream-variant-2KB | SUMO3 | GRCh38.p7 | 21:44818196 | GCCGCGGCTCTGGGC[C/G]GTTGGAGATGCGTCA | 6612 |
rs758734393 | snp | G/T | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44815932 | AGCTATCCAGGGAAG[G/T]CAGAACCATTCTCCT | 6612 |
rs758926178 | snp | A/G | 0.000115927 | 0.0076125 | missense, intron-variant | SUMO3 | GRCh38.p7 | 21:44813891 | TCTGGGTCCAGCCCC[A/G]AGACGCTCGTGCTCT | 6612 |
rs758969280 | in-del | -/G | | | downstream-variant-500B | SUMO3, LINC01424 | GRCh38.p7 | 21:44805136 | GCTCATTTTCAACCT[-/G]GGTTTTGTTACACCA | 6612 |
rs759014236 | snp | C/G | 3.30306e-05 | 0.00406377 | intron-variant | SUMO3 | GRCh38.p7 | 21:44809039 | ACCACGCGAAGCCAG[C/G]TCCGTACCTGTGCTG | 6612 |
rs759017618 | snp | C/T | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44813399 | GACACACACACACCA[C/T]GTCACAAACAGCAGC | 6612 |
rs759084276 | snp | A/C | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44812785 | ATGTACACGGCCCCA[A/C]ACGCCTGCCATCCCG | 6612 |
rs759104419 | snp | C/T | 1.64841e-05 | 0.00287085 | intron-variant | SUMO3 | GRCh38.p7 | 21:44808966 | CTCCCACCTACAATT[C/T]TCAAATAAGCGTATC | 6612 |
rs759261678 | snp | C/T | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44814714 | ACTCCCCACAGCAGG[C/T]GGCCAGGCTCCTTCT | 6612 |
rs759395348 | snp | C/T | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44808018 | TGAATAGTAAATATT[C/T]AAAATCTTAAATGTT | 6612 |
rs759444288 | snp | A/G | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44808390 | TGGTGGTGGGCACCT[A/G]TAGTCCCAGCTACTT | 6612 |
rs759706711 | snp | A/G | 1.68261e-05 | 0.00290048 | synonymous-codon, intron-variant | SUMO3 | GRCh38.p7 | 21:44813943 | GACCAGTGCGCACAC[A/G]GGGAGGCTCTGCGGG | 6612 |
rs760167442 | snp | C/T | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44814269 | ATGGTTTTATTTTTA[C/T]ACAGAATTTATTTTT | 6612 |
rs760183238 | snp | A/T | 0.000395648 | 0.0140594 | intron-variant | SUMO3 | GRCh38.p7 | 21:44808606 | TCATTCATGTCTGCA[A/T]GTGCCTGAGAGAAAC | 6612 |
rs760220433 | snp | C/G | | | utr-variant-3-prime | SUMO3 | GRCh38.p7 | 21:44805727 | CCACCCGAGCCCATA[C/G]AGCAAACAGGAAATG | 6612 |
rs760328660 | snp | G/T | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44813481 | GAAACTGGGGAAGAA[G/T]GGGAAAGAATCACGC | 6612 |
rs760412958 | in-del | -/CACACATGCCCACACC | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44810907 | CTCCCAACACAGGCA[-/CACACATGCCCACACC]CACACATGCCCACAC | 6612 |
rs760533201 | snp | A/G | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44816025 | GTCAGAGCCCCAGAG[A/G]GCAGAGCTGCTCCCA | 6612 |
rs760699725 | snp | A/C | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44808453 | AGGAGGCAGAGCTTG[A/C]ACAGTGAGCTGAGAC | 6612 |
rs760991904 | snp | C/G | 1.65455e-05 | 0.00287619 | intron-variant | SUMO3 | GRCh38.p7 | 21:44814138 | ACTGGCCTCAAAACT[C/G]TGTCTCAAAATAACC | 6612 |
rs761150846 | snp | C/T | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44810441 | CTGCCTGGAAGTTCA[C/T]ATGCAGACCCCTCAG | 6612 |
rs761483756 | snp | A/G | | | utr-variant-3-prime | SUMO3 | GRCh38.p7 | 21:44806031 | ACCACACTTGGAAGT[A/G]GCTCTTATACACGAC | 6612 |
rs761553689 | snp | C/T | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44814991 | GGGGCACCCCTCTGC[C/T]GGCCTGCACTGCTGG | 6612 |
rs761729322 | snp | C/T | 3.29571e-05 | 0.00405924 | missense | SUMO3 | GRCh38.p7 | 21:44809073 | TGTCAGTTTCATTGA[C/T]TGGCTGCCCGTCGAA | 6612 |
rs762005203 | snp | G/T | | | upstream-variant-2KB | SUMO3 | GRCh38.p7 | 21:44819043 | AAGGCGGGGGAGGCC[G/T]CACTTCAGGCTCAGC | 6612 |
rs762068746 | snp | A/G | | | upstream-variant-2KB | SUMO3 | GRCh38.p7 | 21:44819170 | TGGAGACAAGTCTTC[A/G]TGGACCATAACTTCA | 6612 |
rs762099154 | snp | A/G | | | utr-variant-3-prime | SUMO3 | GRCh38.p7 | 21:44806631 | GGCCAGACTAAAAGC[A/G]AACATTCAGGCTATA | 6612 |
rs762327647 | snp | C/T | 1.65252e-05 | 0.00287443 | intron-variant | SUMO3 | GRCh38.p7 | 21:44814118 | TCCTGCAGAAGACAC[C/T]AGAGACTGGCCTCAA | 6612 |
rs762591470 | snp | A/G | 0.000134499 | 0.00819948 | intron-variant | SUMO3 | GRCh38.p7 | 21:44813851 | CGCCTGCCCATCCAC[A/G]AAGAGGGCACCTCGG | 6612 |
rs762743205 | snp | A/G | 1.64988e-05 | 0.00287213 | splice-donor-variant | SUMO3 | GRCh38.p7 | 21:44809045 | CGAAGCCAGCTCCGT[A/G]CCTGTGCTGGAGTGT | 6612 |
rs762826588 | snp | C/T | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44815145 | CATCACACGCCTGTT[C/T]TCTCCACTTCTCCTT | 6612 |
rs762891518 | snp | A/G | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44816323 | AGTGGGAGAACTTTG[A/G]CTTCACTGGAGTCAA | 6612 |
rs762927886 | snp | C/G | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44808610 | TCATGTCTGCATGTG[C/G]CTGAGAGAAACGAGC | 6612 |
rs762972776 | in-del | -/T | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44808224 | TTTAAAAAAAAACTC[-/T]TGTTTCGGCCGGGCG | 6612 |
rs762992147 | snp | A/G | 1.65097e-05 | 0.00287308 | missense | SUMO3 | GRCh38.p7 | 21:44814091 | ATGTGGTCATTCTCT[A/G]TCTTCACACCCTCCT | 6612 |
rs763006303 | snp | C/T | | | upstream-variant-2KB | SUMO3 | GRCh38.p7 | 21:44819704 | AGTGATGCGTGACTA[C/T]AGTCATGGATAAGGG | 6612 |
rs763057306 | snp | A/G | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44809585 | ACGTCCTAGACTAAC[A/G]TCCAAACTCATGTAC | 6612 |
rs763152816 | in-del | -/ATAT | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44811122 | CATGCACACACCCAC[-/ATAT]ACACACAGGCACACA | 6612 |
rs763162224 | snp | C/T | | | upstream-variant-2KB | SUMO3 | GRCh38.p7 | 21:44819161 | GCAAAGCCATGGAGA[C/T]AAGTCTTCATGGACC | 6612 |
rs763297398 | snp | C/G | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44808555 | CAAAGCTCTTTCCAT[C/G]ACAGTATGATGCCCT | 6612 |
rs763390255 | in-del | -/A | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44814844 | TTTAATTCATGCCAT[-/A]ACTTGAAGCTACTCA | 6612 |
rs763749389 | snp | C/T | 3.89727e-05 | 0.00441416 | intron-variant | SUMO3 | GRCh38.p7 | 21:44808999 | AAATGGCAGTTACCC[C/T]GCACAAATCGGAAGT | 6612 |
rs763868593 | snp | C/T | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44808484 | TGCGCCACTGCATTC[C/T]AGCCTGGGCAACAAA | 6612 |
rs763969422 | snp | A/G | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44809196 | CCATTAGTCTCACTG[A/G]CAAGCCCTGGAGAGG | 6612 |
rs764098178 | snp | C/G | 1.64936e-05 | 0.00287168 | missense | SUMO3 | GRCh38.p7 | 21:44809047 | AAGCCAGCTCCGTAC[C/G]TGTGCTGGAGTGTCA | 6612 |
rs764541697 | snp | C/G | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44817186 | ATGGGGAGGCGTGGG[C/G]GTACACCGGGGGGCG | 6612 |
rs764685580 | snp | C/T | | | upstream-variant-2KB | SUMO3 | GRCh38.p7 | 21:44819978 | GAGCTCAGGAAAAAC[C/T]GTGGCCTACCACGAG | 6612 |
rs764729100 | snp | A/T | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44815012 | GCACTGCTGGGATAA[A/T]GTCGTTTGTGAGTGA | 6612 |
rs764876567 | snp | C/T | | | utr-variant-3-prime | SUMO3 | GRCh38.p7 | 21:44806043 | AGTAGCTCTTATACA[C/T]GACAACATAACTGCA | 6612 |
rs764949105 | snp | C/G | 1.65438e-05 | 0.00287605 | intron-variant | SUMO3 | GRCh38.p7 | 21:44814140 | TGGCCTCAAAACTGT[C/G]TCTCAAAATAACCGC | 6612 |
rs765135625 | snp | C/T | 2.50009e-05 | 0.00353551 | intron-variant | SUMO3 | GRCh38.p7 | 21:44808976 | CAATTCTCAAATAAG[C/T]GTATCCCAAATGGCA | 6612 |
rs765250850 | snp | C/G | | | upstream-variant-2KB | SUMO3 | GRCh38.p7 | 21:44819061 | CTTCAGGCTCAGCTG[C/G]GAAATGGCAGGGCCT | 6612 |
rs765382230 | snp | G/T | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44808242 | TTTCGGCCGGGCGCG[G/T]TGGCTCATGCCTTTA | 6612 |
rs765658154 | snp | C/T | 3.42706e-05 | 0.00413934 | utr-variant-3-prime | SUMO3 | GRCh38.p7 | 21:44806923 | ACAGCAATGCGAGGA[C/T]GGACGGCCCGGGCTG | 6612 |
rs765828616 | snp | A/C | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44811632 | AGAAAGAAAAAAGAA[A/C]TTTTGGAAATTAAAA | 6612 |
rs766360555 | snp | A/C | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44814595 | AGTCATGCAGCTATA[A/C]AGCACTAGTAAAAGA | 6612 |
rs766420873 | snp | A/G | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44809641 | TACGAAACCCAGGTG[A/G]GGAAGCGTAACACGT | 6612 |
rs766654289 | snp | C/T | | | upstream-variant-2KB | SUMO3 | GRCh38.p7 | 21:44819710 | GCGTGACTACAGTCA[C/T]GGATAAGGGAAAAAG | 6612 |
rs766770441 | snp | C/G | 7.67961e-05 | 0.00619614 | missense, intron-variant | SUMO3 | GRCh38.p7 | 21:44813871 | GGGCACCTCGGGCAG[C/G]TGCATCTGGGTCCAG | 6612 |
rs767036683 | snp | C/T | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44813428 | GCCAGAAGGCATCCA[C/T]CCAGCTGGGCACTGC | 6612 |
rs767084965 | snp | C/T | 3.38432e-05 | 0.00411345 | utr-variant-3-prime | SUMO3 | GRCh38.p7 | 21:44806930 | TGCGAGGATGGACGG[C/T]CCGGGCTGGGGACGG | 6612 |
rs767198239 | snp | A/G | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44812800 | CACGCCTGCCATCCC[A/G]CAGCGCAGAGGAGAA | 6612 |
rs767384489 | snp | C/T | 9.99201e-05 | 0.00706753 | missense, intron-variant | SUMO3 | GRCh38.p7 | 21:44813864 | ACGAAGAGGGCACCT[C/T]GGGCAGCTGCATCTG | 6612 |
rs767509168 | snp | G/T | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44807192 | CGTCCCCTCACTGCA[G/T]CTCAGCACGCATGGA | 6612 |
rs767629856 | snp | A/G | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44808231 | AAAAAACTCTGTTTC[A/G]GCCGGGCGCGTTGGC | 6612 |
rs767670376 | snp | A/G | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44813330 | CATAAAAGTGGCCTA[A/G]AGAGGGACCCCCTGG | 6612 |
rs767672098 | snp | C/T | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44809770 | GAGCCGCCAGGTGAA[C/T]ACTAACCTTCCAGTG | 6612 |
rs767678215 | snp | C/T | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44808278 | AGCACTTTGGGGGGC[C/T]GAGGTGGGCAGATCA | 6612 |
rs767834690 | snp | A/G | 3.29549e-05 | 0.00405911 | synonymous-codon | SUMO3 | GRCh38.p7 | 21:44809083 | ATTGATTGGCTGCCC[A/G]TCGAACCTGAATCTG | 6612 |
rs767949526 | in-del | -/T | | | upstream-variant-2KB | SUMO3 | GRCh38.p7 | 21:44819739 | GAGGCTCAGATGACA[-/T]TTAGGTTTTAAAAAG | 6612 |
rs767972690 | snp | A/G | 1.65285e-05 | 0.00287471 | intron-variant | SUMO3 | GRCh38.p7 | 21:44814121 | TGCAGAAGACACCAG[A/G]GACTGGCCTCAAAAC | 6612 |
rs768107279 | snp | C/T | | | upstream-variant-2KB | SUMO3 | GRCh38.p7 | 21:44819319 | CATAAGGTGTGGTCC[C/T]TTCCTTCTGGAACCT | 6612 |
rs768256587 | snp | C/T | 1.78998e-05 | 0.00299159 | missense, intron-variant | SUMO3 | GRCh38.p7 | 21:44813912 | CTCGTGCTCTGGGGA[C/T]GCCTGGAACGCACAG | 6612 |
rs768467583 | snp | A/T | 6.12276e-05 | 0.00553264 | intron-variant | SUMO3 | GRCh38.p7 | 21:44813855 | TGCCCATCCACGAAG[A/T]GGGCACCTCGGGCAG | 6612 |
rs768477988 | snp | C/T | 4.55519e-05 | 0.0047722 | utr-variant-3-prime | SUMO3 | GRCh38.p7 | 21:44806882 | AGACACCTTTGTGGT[C/T]GGCATGGTCACGTGC | 6612 |
rs768524150 | snp | A/G | | | upstream-variant-2KB | SUMO3 | GRCh38.p7 | 21:44818684 | CTGTGAAGAAACTGA[A/G]GCACTGGGAGGTCAA | 6612 |
rs768685059 | snp | A/G | 1.6513e-05 | 0.00287336 | synonymous-codon | SUMO3 | GRCh38.p7 | 21:44814099 | ATTCTCTGTCTTCAC[A/G]CCCTCCTGCAGAAGA | 6612 |
rs768993649 | in-del | -/TG | 1.6546e-05 | 0.00287624 | intron-variant | SUMO3 | GRCh38.p7 | 21:44814137 | GACTGGCCTCAAAAC[-/TG]TGTCTCAAAATAACC | 6612 |
rs769110131 | snp | C/T | 0.000412814 | 0.0143609 | utr-variant-3-prime | SUMO3 | GRCh38.p7 | 21:44806893 | TGGTCGGCATGGTCA[C/T]GTGCTCACCATTCAA | 6612 |
rs769165329 | snp | C/T | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44807571 | GTAGTGAAACACCCC[C/T]GCTCACTTCTCTCCT | 6612 |
rs769217032 | snp | A/C | 1.66835e-05 | 0.00288816 | intron-variant | SUMO3 | GRCh38.p7 | 21:44809025 | GAAGTCGCCCTGGAA[A/C]CACGCGAAGCCAGCT | 6612 |
rs769253131 | snp | C/T | 4.9525e-05 | 0.00497595 | intron-variant | SUMO3 | GRCh38.p7 | 21:44809042 | ACGCGAAGCCAGCTC[C/T]GTACCTGTGCTGGAG | 6612 |
rs769339182 | in-del | -/A | 0.222676 | 0.248502 | intron-variant | SUMO3 | GRCh38.p7 | 21:44808514 | GCGAGACTCCGTCTC[-/A]AAAAAAAAAAGTCTG | 6612 |
rs769451719 | snp | C/T | 1.68255e-05 | 0.00290043 | intron-variant | SUMO3 | GRCh38.p7 | 21:44813846 | GCCCCCGCCTGCCCA[C/T]CCACGAAGAGGGCAC | 6612 |
rs769543976 | snp | C/T | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44816197 | AAAATTAATATCATA[C/T]GTATTTTATTACATT | 6612 |
rs769731824 | in-del | -/CT | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44807183 | GCTCTTGTCCGTCCC[-/CT]CACTGCAGCTCAGCA | 6612 |
rs769783367 | snp | A/T | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44810954 | CACACACATGCACAC[A/T]CCCACACATGCACAC | 6612 |
rs770045480 | snp | G/T | 1.65056e-05 | 0.00287272 | missense | SUMO3 | GRCh38.p7 | 21:44814080 | CCTTCAGGTTGATGT[G/T]GTCATTCTCTGTCTT | 6612 |
rs770147730 | snp | C/T | 0.000167659 | 0.0091543 | intron-variant | SUMO3 | GRCh38.p7 | 21:44808323 | CGAGACCATCCTGGC[C/T]AACATGGTGAAACCC | 6612 |
rs770256989 | snp | A/G | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44812542 | TGTCTCAAAGACGCT[A/G]CCCTTCTGTGCCCGT | 6612 |
rs770279294 | in-del | -/TA | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44814404 | AATCCATCTTTATTT[-/TA]AAGTTATTCTTGTGG | 6612 |
rs770424325 | snp | A/G | 0.000889284 | 0.0210678 | intron-variant | SUMO3 | GRCh38.p7 | 21:44808420 | TGGGAGGCTGAGGCA[A/G]GAGAATGGCGTGAAC | 6612 |
rs770438614 | snp | C/T | 3.33133e-05 | 0.00408112 | missense | SUMO3 | GRCh38.p7 | 21:44807025 | CGTCGATGGTGTCCT[C/T]GTCCTCCATCTCCAG | 6612 |
rs770440262 | in-del | -/CACATATGCACACACG | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44811011 | ACACATGCACACACC[-/CACATATGCACACACG]CACACACCCACATAC | 6612 |
rs770481330 | snp | C/T | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44815850 | TAATAAGCAAGTGAA[C/T]TCGTGAGTTAAAAAG | 6612 |
rs770768131 | snp | C/T | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44808345 | GTGAAACCCCGTCTC[C/T]ACTAAAAATACAAAA | 6612 |
rs770865538 | snp | C/T | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44812145 | CCCTGCAGCCTCCAC[C/T]TCCTGGGCTCAAACA | 6612 |
rs770874197 | snp | C/T | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44816423 | CAAGCAGAGTGCAGA[C/T]TTCCATAGAGGCCGC | 6612 |
rs770939465 | in-del | -/A | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44810117 | TGGAGAAATGTGGTC[-/A]GGGGCAGAAACATTT | 6612 |
rs771011901 | in-del | -/AT | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44810496 | CCCACGGCAGCACAC[-/AT]ATGAGATGTGCTTTC | 6612 |
rs771240331 | snp | C/T | | | downstream-variant-500B | SUMO3 | GRCh38.p7 | 21:44805495 | GCGAATACTAACCTT[C/T]CAGCGGCTAGCTTTT | 6612 |
rs771282422 | snp | C/G | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44812617 | GGGAGGAGGACTAAT[C/G]CAGGAAACACCCAAG | 6612 |
rs771706345 | in-del | -/TATGCACA | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44811015 | ATGCACACACCCACA[-/TATGCACA]CACGCACACACCCAC | 6612 |
rs771738656 | in-del | -/AC | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44813385 | TACCAAGAACAACAG[-/AC]ACACACACACCACGT | 6612 |
rs771971759 | snp | A/G | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44808393 | TGGTGGGCACCTATA[A/G]TCCCAGCTACTTGGG | 6612 |
rs772137415 | snp | A/G | 3.42536e-05 | 0.00413831 | synonymous-codon, intron-variant | SUMO3 | GRCh38.p7 | 21:44813922 | GGGGATGCCTGGAAC[A/G]CACAGGACCAGTGCG | 6612 |
rs772323945 | in-del | -/CACACATA | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44811168 | ACACAGGCACACACC[-/CACACATA]CACACATACACACAC | 6612 |
rs772464399 | snp | C/T | 1.64933e-05 | 0.00287165 | intron-variant | SUMO3 | GRCh38.p7 | 21:44809159 | AGTCTCACTGGCAAG[C/T]CCTGGAAAGGAAAAG | 6612 |
rs772513616 | snp | A/T | | | downstream-variant-500B | SUMO3 | GRCh38.p7 | 21:44805616 | TTAGTAGAAGCCAAG[A/T]GACAGAATACCAAAC | 6612 |
rs772627637 | snp | A/G | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44814770 | AGGGAAGCCACCTCC[A/G]AGTACTTTCTGGTTT | 6612 |
rs772734033 | snp | A/C | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44816247 | GCCACCTACAAAAAC[A/C]TAAAGGACATTTATA | 6612 |
rs772787270 | snp | C/G | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44807725 | GGAGTCCCATCAGGG[C/G]TGTCGGCCACCCTCA | 6612 |
rs773132003 | snp | G/T | 1.69292e-05 | 0.00290935 | synonymous-codon, intron-variant | SUMO3 | GRCh38.p7 | 21:44813934 | AACGCACAGGACCAG[G/T]GCGCACACGGGGAGG | 6612 |
rs773133140 | snp | C/T | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44811017 | GCACACACCCACATA[C/T]GCACACACGCACACA | 6612 |
rs773149030 | snp | A/G | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44813031 | CTCAGCAAACACAAA[A/G]AAAGGAAGTCAGGGG | 6612 |
rs773288927 | snp | C/T | | | upstream-variant-2KB | SUMO3 | GRCh38.p7 | 21:44819678 | AAATTACGCCAGTTG[C/T]TGTGTCACGAAGTGA | 6612 |
rs773532443 | snp | A/G | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44808510 | ACAAAGCGAGACTCC[A/G]TCTCAAAAAAAAAAG | 6612 |
rs773663502 | snp | A/G | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44812561 | TTCTGTGCCCGTTCT[A/G]ACAAGACCCTGGAGG | 6612 |
rs774399267 | snp | C/G | 1.66838e-05 | 0.00288818 | intron-variant | SUMO3 | GRCh38.p7 | 21:44813857 | CCCATCCACGAAGAG[C/G]GCACCTCGGGCAGCT | 6612 |
rs774403963 | snp | A/G | | | upstream-variant-2KB | SUMO3 | GRCh38.p7 | 21:44819853 | TGACAGCAAAGATGC[A/G]AAAAGGCTCTGTCGC | 6612 |
rs774410433 | in-del | -/C | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44815943 | GAAGTCAGAACCATT[-/C]TCCTGCCTGACCTAA | 6612 |
rs774441467 | snp | A/G | 1.65209e-05 | 0.00287405 | intron-variant | SUMO3 | GRCh38.p7 | 21:44814110 | TCACACCCTCCTGCA[A/G]AAGACACCAGAGACT | 6612 |
rs774531863 | snp | C/T | | | missense | SUMO3 | GRCh38.p7 | 21:44814092 | TGTGGTCATTCTCTG[C/T]CTTCACACCCTCCTG | 6612 |
rs774560624 | snp | A/G | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44812681 | GAGGCCCTGGACCAC[A/G]GCTGAGCAGCCAGCC | 6612 |
rs774591189 | in-del | -/GAGCGGCGCGGGG | 8.17996e-05 | 0.00639477 | utr-variant-5-prime | SUMO3 | GRCh38.p7 | 21:44817977 | CGGACATGGCTGCGC[-/GAGCGGCGCGGGG]AGGCGGCGCGGGGGA | 6612 |
rs774668230 | in-del | -/G | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44815197 | GACAACTGTCCCAGC[-/G]ATGCCTAAATACAGG | 6612 |
rs774797443 | snp | C/T | 7.07289e-05 | 0.00594638 | intron-variant | SUMO3 | GRCh38.p7 | 21:44813850 | CCGCCTGCCCATCCA[C/T]GAAGAGGGCACCTCG | 6612 |
rs774891433 | snp | A/G | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44813345 | GAGAGGGACCCCCTG[A/G]CCCAGGGTGAGTCCG | 6612 |
rs775022504 | in-del | -/CAGA | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44808751 | ACAACAGCAAGCGTC[-/CAGA]CAATGAGTGGGAAGG | 6612 |
rs775261384 | snp | C/G | | | upstream-variant-2KB | SUMO3 | GRCh38.p7 | 21:44818707 | GAGGTCAAACCACCC[C/G]CAGGTCAGCGCTGGT | 6612 |
rs775377292 | snp | A/G | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44808452 | CAGGAGGCAGAGCTT[A/G]CACAGTGAGCTGAGA | 6612 |
rs775467351 | snp | A/C | | | upstream-variant-2KB | SUMO3 | GRCh38.p7 | 21:44818551 | AGACGATTGGGGGCG[A/C]CACCCGCCTCCCTGC | 6612 |
rs775545313 | snp | A/C | 4.9948e-05 | 0.00499715 | missense, splice-donor-variant | SUMO3 | GRCh38.p7 | 21:44813974 | GGAGCAAGGTGCCGC[A/C]CCTGCCTCTCGCAGT | 6612 |
rs775590911 | snp | A/G | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44811349 | GAGACCGAGGCAGAA[A/G]GATCACTTAAGCCCA | 6612 |
rs775608571 | in-del | -/GCACA | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44817756 | GGGGCGGAGCTCGCG[-/GCACA]GCGCGCTTCGCGGGG | 6612 |
rs775739484 | snp | C/T | 1.65091e-05 | 0.00287303 | synonymous-codon | SUMO3 | GRCh38.p7 | 21:44814090 | GATGTGGTCATTCTC[C/T]GTCTTCACACCCTCC | 6612 |
rs775935007 | snp | A/C/G | 3.3319e-05 | 0.0040815 | missense, synonymous-codon | SUMO3 | GRCh38.p7 | 21:44807026 | GTCGATGGTGTCCTC[A/C/G]TCCTCCATCTCCAGC | 6612 |
rs775974515 | snp | C/G | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44814866 | AGCTACTCAACAATG[C/G]CACAATCGGGGTGTC | 6612 |
rs776060888 | snp | A/C | | | utr-variant-3-prime | SUMO3 | GRCh38.p7 | 21:44805688 | ACAAATTGGTGAATA[A/C]ACACAACAGAGCCAA | 6612 |
rs776113624 | snp | C/T | 2.64638e-05 | 0.00363747 | intron-variant | SUMO3 | GRCh38.p7 | 21:44808957 | CTGTATGAGCTCCCA[C/T]CTACAATTCTCAAAT | 6612 |
rs776123573 | snp | A/G | | | utr-variant-3-prime | SUMO3 | GRCh38.p7 | 21:44806894 | GGTCGGCATGGTCAC[A/G]TGCTCACCATTCAAC | 6612 |
rs776199505 | snp | C/G | 0.000984252 | 0.0221621 | intron-variant | SUMO3 | GRCh38.p7 | 21:44808449 | ACTCAGGAGGCAGAG[C/G]TTGCACAGTGAGCTG | 6612 |
rs776311171 | snp | C/T | 3.29462e-05 | 0.00405857 | missense, intron-variant | SUMO3 | GRCh38.p7 | 21:44813971 | GGGGGAGCAAGGTGC[C/T]GCACCTGCCTCTCGC | 6612 |
rs776314670 | snp | A/G | 1.65679e-05 | 0.00287814 | intron-variant | SUMO3 | GRCh38.p7 | 21:44809031 | GCCCTGGAACCACGC[A/G]AAGCCAGCTCCGTAC | 6612 |
rs776428731 | snp | A/T | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44809544 | GAAGGAAAGCCGACT[A/T]ACATTCAAACACCAG | 6612 |
rs776665499 | snp | G/T | | | upstream-variant-2KB | SUMO3 | GRCh38.p7 | 21:44819103 | TAAGCGTCTGAGCCG[G/T]TTCTGTCCTGCCTGG | 6612 |
rs776805257 | snp | C/T | 9.96678e-05 | 0.00705861 | synonymous-codon | SUMO3 | GRCh38.p7 | 21:44806993 | CTCCGGCACACCTCC[C/T]GTCTGCTGCTGGAAC | 6612 |
rs776985462 | snp | A/G | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44812521 | AAGTCACGTTCAGCC[A/G]TGCAGTGTCTCAAAG | 6612 |
rs777052109 | snp | A/G | 5.21453e-05 | 0.00510587 | utr-variant-3-prime | SUMO3 | GRCh38.p7 | 21:44806918 | ATTCAACAGCAATGC[A/G]AGGATGGACGGCCCG | 6612 |
rs777105039 | snp | A/G | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44807600 | CTCCTGACACAGTGG[A/G]CGCAAAACACCCACC | 6612 |
rs777135428 | in-del | -/A | | | utr-variant-3-prime | SUMO3 | GRCh38.p7 | 21:44806610 | CAACTCAGGAGTCAG[-/A]TCCCTGGCCAGACTA | 6612 |
rs777226001 | snp | C/T | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44817586 | AGCACGCAAAGACGC[C/T]TCGGGGACACTGCTG | 6612 |
rs777359912 | snp | C/T | 3.3195e-05 | 0.00407387 | intron-variant | SUMO3 | GRCh38.p7 | 21:44814155 | GTCTCAAAATAACCG[C/T]GACTTGAATGGGCAA | 6612 |
rs777360247 | in-del | -/CA | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44810987 | ATGCACACACCCATG[-/CA]CACACCCACACATGC | 6612 |
rs777427190 | snp | C/G | | | upstream-variant-2KB | SUMO3 | GRCh38.p7 | 21:44819399 | CGGTCCTGGGAGGGG[C/G]CTCCGCAACCAGCCC | 6612 |
rs777455217 | snp | C/T | 1.65162e-05 | 0.00287365 | synonymous-codon | SUMO3 | GRCh38.p7 | 21:44814039 | CTTGATCTTGAACTG[C/T]ACCACGGAGCCGTCC | 6612 |
rs777538692 | snp | C/T | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44815806 | CTCCAAACAGAATGA[C/T]GATCTGTCCCAGACC | 6612 |
rs777580377 | snp | C/T | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44812851 | CACACACAGTGGCCA[C/T]GAGCCCAGGCAGTAC | 6612 |
rs777642308 | snp | A/G | | | downstream-variant-500B | SUMO3, LINC01424 | GRCh38.p7 | 21:44805165 | CACTGCACACTGGGA[A/G]ATTCTTAAAGCCAAA | 6612 |
rs777737843 | snp | A/T | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44811987 | AGAATATGGTCCCAG[A/T]TACTTCCAGGGAAAA | 6612 |
rs777906810 | snp | C/G | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44814678 | CAAGTGGTGATTTCG[C/G]GAATCCAACTGAGGA | 6612 |
rs777914527 | snp | C/T | 1.66131e-05 | 0.00288206 | missense | SUMO3 | GRCh38.p7 | 21:44806977 | GCCCTGCCAGGCTGC[C/T]CTCCGGCACACCTCC | 6612 |
rs778055721 | snp | A/C | 2.26129e-05 | 0.00336243 | synonymous-codon, intron-variant | SUMO3 | GRCh38.p7 | 21:44813892 | CTGGGTCCAGCCCCG[A/C]GACGCTCGTGCTCTG | 6612 |
rs778133803 | snp | A/G | 0.000250137 | 0.0111806 | intron-variant | SUMO3 | GRCh38.p7 | 21:44809000 | AATGGCAGTTACCCC[A/G]CACAAATCGGAAGTC | 6612 |
rs778141401 | snp | C/T | 5.12658e-05 | 0.00506264 | intron-variant | SUMO3 | GRCh38.p7 | 21:44813836 | TACAGCACAAGCCCC[C/T]GCCTGCCCATCCACG | 6612 |
rs778277417 | snp | A/G | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44812247 | ATGTTTCGTAGAGAC[A/G]GGGTCTCCCTGTGTT | 6612 |
rs778388162 | snp | C/G | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44809859 | CACTGAATCTTCTCT[C/G]TCCTGGTGCCCTGAC | 6612 |
rs778416749 | snp | A/G | 1.66579e-05 | 0.00288595 | synonymous-codon, intron-variant | SUMO3 | GRCh38.p7 | 21:44813958 | GGGGAGGCTCTGCGG[A/G]GGAGCAAGGTGCCGC | 6612 |
rs778485624 | snp | C/T | 1.65302e-05 | 0.00287486 | missense | SUMO3 | GRCh38.p7 | 21:44814017 | GCTTGCTCAGCGGCG[C/T]GTGCCTCTTGATCTT | 6612 |
rs778598984 | snp | C/T | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44809895 | CTGGGTCATCCCTCC[C/T]ATCTTTCCAGAAGCC | 6612 |
rs778607768 | snp | G/T | | | upstream-variant-2KB | SUMO3 | GRCh38.p7 | 21:44820000 | TACCACGAGCACAGG[G/T]TAAAGAACCCAAATG | 6612 |
rs778617766 | snp | G/T | 1.67248e-05 | 0.00289173 | utr-variant-3-prime | SUMO3 | GRCh38.p7 | 21:44806940 | GACGGCCCGGGCTGG[G/T]GACGGGCCCTCTAGA | 6612 |
rs778707512 | snp | A/G | | | upstream-variant-2KB | SUMO3 | GRCh38.p7 | 21:44819461 | CAGATTGCTGGCCCT[A/G]GAAGTGCCCTAGGGC | 6612 |
rs778707979 | snp | A/C/G | 0.000224278 | 0.0105874 | | | GRCh38.p7 | 21:44806883 | GACACCTTTGTGGTC[A/C/G]GCATGGTCACGTGCT | 6612 |
rs778760404 | snp | C/T | | | upstream-variant-2KB | SUMO3 | GRCh38.p7 | 21:44820029 | TGGCCAGAGCCCCTC[C/T]GGAGGGTCGCCACAC | 6612 |
rs778899020 | snp | C/G | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44812982 | GTGTCTGGAAGCTCA[C/G]TCTCACCTTTCGCAG | 6612 |
rs778994356 | snp | C/G | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44815534 | GTGGCCTCCAGCACA[C/G]AGACAACTGGCCTAG | 6612 |
rs779043784 | snp | C/T | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44807417 | ACTGAGTCCTAGGAC[C/T]CACAGGAGCCTTGCG | 6612 |
rs779183913 | snp | A/G | | | utr-variant-3-prime | SUMO3 | GRCh38.p7 | 21:44806666 | TGGGGTTAAAAAAAT[A/G]TTGTAGGAGGGGGGG | 6612 |
rs779256756 | snp | A/G | 3.09516e-05 | 0.00393381 | missense, intron-variant | SUMO3 | GRCh38.p7 | 21:44813881 | GGCAGCTGCATCTGG[A/G]TCCAGCCCCGAGACG | 6612 |
rs779343609 | snp | A/G | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44814731 | GCCAGGCTCCTTCTC[A/G]CTGCCCTGACATCAG | 6612 |
rs779382696 | snp | C/T | | | utr-variant-3-prime | SUMO3 | GRCh38.p7 | 21:44806820 | GTTGCACTTGAAGTA[C/T]ATCAAAGAGAGGAAA | 6612 |
rs779980708 | snp | C/T | | | downstream-variant-500B | SUMO3 | GRCh38.p7 | 21:44805327 | CCCTTTCTTTACATA[C/T]GAAACCCAGGAGAGG | 6612 |
rs780223287 | snp | C/T | 1.64768e-05 | 0.00287021 | missense | SUMO3 | GRCh38.p7 | 21:44809105 | CTGAATCTGATCTGC[C/T]TCATTGACAAGCCCT | 6612 |
rs780505332 | in-del | -/C | 1.65482e-05 | 0.00287643 | frameshift-variant | SUMO3 | GRCh38.p7 | 21:44813998 | CGCAGTAGGCCTTCA[-/C]TCAGCTTGCTCAGCG | 6612 |
rs780540557 | snp | C/T | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44815747 | GGAATGGCTGCAGCC[C/T]CGGGAGAGGCTGGGG | 6612 |
rs780717596 | in-del | -/TG | 1.6631e-05 | 0.00288362 | frameshift-variant | SUMO3 | GRCh38.p7 | 21:44806959 | GGGCCCTCTAGAAAC[-/TG]TGCCCTGCCAGGCTG | 6612 |
rs780800537 | snp | C/T | 5.43715e-05 | 0.00521371 | utr-variant-3-prime | SUMO3 | GRCh38.p7 | 21:44806864 | ATGTCCTCGAGTTTC[C/T]GCAGACACCTTTGTG | 6612 |
rs781050103 | snp | C/T | 0.0259695 | 0.110952 | utr-variant-5-prime | SUMO3 | GRCh38.p7 | 21:44817983 | TGGCTGCGCGAGCGG[C/T]GCGGGGAGGCGGCGC | 6612 |
rs781221744 | snp | C/T | | | upstream-variant-2KB | SUMO3 | GRCh38.p7 | 21:44818624 | AACGCTCCTACGGGG[C/T]TGCCCCGGGCCCTCC | 6612 |
rs781457735 | snp | A/G | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44811795 | GGACAATGAGCAGCA[A/G]GAGGAACAGGAACTC | 6612 |
rs781691047 | snp | A/G | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44808295 | AGGTGGGCAGATCAC[A/G]AGGTCAGGAGATCGA | 6612 |
rs796071097 | snp | A/C | | | utr-variant-3-prime | SUMO3 | GRCh38.p7 | 21:44806639 | TAAAAGCGAACATTC[A/C]GGCTATAATTTTGGG | 6612 |
rs796454160 | snp | A/G | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44809741 | CATTGGTGATGTGCC[A/G]GGGGAGGGGAAATGA | 6612 |
rs796569293 | in-del | -/CACA | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44810995 | ACCCATGCACACACC[-/CACA]CATGCACACACCCAC | 6612 |
rs796602003 | snp | A/G | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44814198 | TTGTTGGCTTTTTAA[A/G]GTCATCAAAACCAAC | 6612 |
rs796787190 | in-del | -/AC | | | intron-variant | SUMO3 | GRCh38.p7 | 21:44811040 | CGCACACACCCACAT[-/AC]ACACACGCACACACC | 6612 |