SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs731570 | snp | A/T | 0.424037 | 0.179474 | intron-variant | DTX1 | GRCh38.p7 | 12:113059814 | CCACATGTGGCTACT[A/T]AAATTTACATTAATT | 1840 |
rs733174 | snp | C/T | 0.264906 | 0.249555 | intron-variant | DTX1 | GRCh38.p7 | 12:113060540 | TTAAATGTCCTCTGC[C/T]CCTTCCTACCCCAGG | 1840 |
rs737633 | snp | A/G | 0.163564 | 0.234582 | intron-variant | DTX1 | GRCh38.p7 | 12:113066920 | GGACACAACTATGCG[A/G]GACCTAGAGGAGACT | 1840 |
rs936386 | snp | A/G | 0.0629771 | 0.165899 | intron-variant | DTX1 | GRCh38.p7 | 12:113065366 | GGGCCGTGCGCACCC[A/G]GCTGCAGACCTGGAT | 1840 |
rs1074161 | snp | C/T | 0.149999 | 0.229128 | intron-variant | DTX1 | GRCh38.p7 | 12:113081938 | CCACTGATGGCAGCA[C/T]CAAGCCCAGGCTTCC | 1840 |
rs1284866 | snp | A/G | 0.373598 | 0.21731 | intron-variant | DTX1 | GRCh38.p7 | 12:113076389 | ctcaatgcaatctcc[A/G]cctccaggttcaagc | 1840 |
rs1284867 | snp | C/T | 0.490398 | 0.0686206 | intron-variant | DTX1 | GRCh38.p7 | 12:113076153 | CTTTTTTTAAATTGA[C/T]ACCTTTATGTATTCT | 1840 |
rs1284868 | snp | C/T | 0.495708 | 0.0461266 | intron-variant | DTX1 | GRCh38.p7 | 12:113069297 | TGGTCACCTGGCTTC[C/T]CACACACCCAGCAGG | 1840 |
rs1284869 | snp | A/G | 0.372189 | 0.218105 | intron-variant | DTX1 | GRCh38.p7 | 12:113068239 | CCTCTGTGGTCAGGA[A/G]TGCAGGGAGGTAGGT | 1840 |
rs1284870 | snp | A/G | 0.319616 | 0.240112 | intron-variant | DTX1 | GRCh38.p7 | 12:113067369 | ATTTCCACAGGGCCA[A/G]GTGAGTAACACCTTG | 1840 |
rs1299753 | snp | A/G | 0.498945 | 0.022939 | intron-variant | DTX1 | GRCh38.p7 | 12:113072908 | accagcctggcccac[A/G]tggtgaaacccccga | 1840 |
rs1300122 | snp | A/G | 0.365439 | 0.221752 | intron-variant | DTX1 | GRCh38.p7 | 12:113076682 | ttcattcaatgattc[A/G]ttcattcattgattc | 1840 |
rs1379862 | snp | A/G | 0 | 0 | intron-variant | DTX1 | GRCh38.p7 | 12:113060624 | CAGGCCTGTACATCC[A/G]GTCCTTGCTCAGCTG | 1840 |
rs1379863 | snp | C/T | 0.116488 | 0.211364 | intron-variant | DTX1 | GRCh38.p7 | 12:113090062 | GATGTCTGCCACAGG[C/T]AGGAGACCAACCAGT | 1840 |
rs1466325 | snp | C/G | 0.474903 | 0.109173 | intron-variant | DTX1 | GRCh38.p7 | 12:113087872 | GGGGACTTGGCTGCC[C/G]TAAAGGGAGGGTCAG | 1840 |
rs1545661 | snp | C/T | 0.099723 | 0.199792 | intron-variant | DTX1 | GRCh38.p7 | 12:113086838 | ACCCTCCCCCACTTT[C/T]CTGCCCCGCTAGCCA | 1840 |
rs1551618 | snp | A/C | 0 | 0 | intron-variant | DTX1 | GRCh38.p7 | 12:113073421 | GGCAGCCTCACTCTG[A/C]TGCCTGATTTATCAT | 1840 |
rs1585243 | snp | C/G | 0.438806 | 0.163867 | intron-variant | DTX1 | GRCh38.p7 | 12:113079601 | GGCACAATCTCCACT[C/G]ACTGCAACTTCTGCC | 1840 |
rs1619738 | snp | C/G | 0.467642 | 0.123012 | intron-variant | DTX1 | GRCh38.p7 | 12:113088479 | ggtcatgcttaaaga[C/G]ggataacattaggag | 1840 |
rs1625170 | snp | A/G | 0.2897 | 0.246828 | intron-variant | DTX1 | GRCh38.p7 | 12:113093490 | CGCCATCCCCGCCCA[A/G]ACCCCCGACCACTGG | 1840 |
rs1625761 | snp | C/T | 0.482008 | 0.0931261 | intron-variant | DTX1 | GRCh38.p7 | 12:113079125 | GTGCCTACCCTGGAC[C/T]CCAGATTCAGTCATC | 1840 |
rs1625812 | snp | A/C | 0.375598 | 0.21616 | intron-variant | DTX1 | GRCh38.p7 | 12:113079147 | TCAGTCATCTGAGCA[A/C]AGAACCAAGCCCTGA | 1840 |
rs1625847 | snp | C/T | 0.370568 | 0.219005 | intron-variant | DTX1 | GRCh38.p7 | 12:113079157 | GAGCAAAGAACCAAG[C/T]CCTGAGGGGTGGCAA | 1840 |
rs1626561 | snp | A/T | 0.466412 | 0.125164 | intron-variant | DTX1 | GRCh38.p7 | 12:113079200 | TCAAAGACCTTGAAC[A/T]TGGGACAGACCAGAA | 1840 |
rs1628251 | snp | A/C | 0.470715 | 0.117409 | intron-variant | DTX1 | GRCh38.p7 | 12:113082891 | GCGTGAGCCACAGCG[A/C]CTGGCCTGTCTCTAT | 1840 |
rs1628639 | snp | C/T | 0.22263 | 0.248497 | intron-variant | DTX1 | GRCh38.p7 | 12:113093094 | TCAGGGGACCTGGCT[C/T]GCCTTCTGTCTCTGG | 1840 |
rs1674089 | snp | A/C | 0.478603 | 0.101197 | intron-variant | DTX1 | GRCh38.p7 | 12:113059024 | GCACGACTCCACCCC[A/C]CAAACCAACACTTGG | 1840 |
rs1674091 | snp | A/G | 0.316485 | 0.240998 | intron-variant | DTX1 | GRCh38.p7 | 12:113090783 | AGTGGGTGTGTGTGC[A/G]CTGCACCTGTGTGCA | 1840 |
rs1674092 | snp | C/T | 0.222333 | 0.248464 | intron-variant | DTX1 | GRCh38.p7 | 12:113091088 | GGGTTTGCTGCCCAC[C/T]TTACCCAGCTCTGTG | 1840 |
rs1674093 | snp | A/G | 0.220843 | 0.248294 | intron-variant | DTX1 | GRCh38.p7 | 12:113091392 | CCTAGTGTGTGCGGT[A/G]TGTTCCCCAAGTAGA | 1840 |
rs1674094 | snp | C/T | 0.268724 | 0.249298 | intron-variant | DTX1 | GRCh38.p7 | 12:113092102 | CAAGAAGTTAAGTGA[C/T]TTGTTCAAGGTTGTC | 1840 |
rs1674095 | snp | A/T | 0.318036 | 0.240564 | intron-variant | DTX1 | GRCh38.p7 | 12:113093500 | GGGGTTTGGGCGGGG[A/T]TGGCGCCCCGCCCTG | 1840 |
rs1674096 | snp | A/G | 0.347914 | 0.230028 | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | RASAL1, DTX1 | GRCh38.p7 | 12:113098391 | AGGACCCTGTCCTTG[A/G]GGAGGAGGGTCAGGT | 1840 |
rs1674117 | snp | A/G | 0.495634 | 0.0465208 | intron-variant | DTX1 | GRCh38.p7 | 12:113086010 | CTGTGGCTCACACCT[A/G]TAATCCCAGCACTTT | 1840 |
rs1674119 | snp | C/T | 0.225005 | 0.248747 | intron-variant | DTX1 | GRCh38.p7 | 12:113088299 | ctgtgttgaggagga[C/T]tctgaagttgcatct | 1840 |
rs1674120 | snp | C/T | 0.313814 | 0.241719 | intron-variant | DTX1 | GRCh38.p7 | 12:113088440 | TGGCAGAAGAGGCgg[C/T]gtggaccagatcata | 1840 |
rs1674122 | snp | A/G | 0.465052 | 0.127485 | intron-variant | DTX1 | GRCh38.p7 | 12:113079689 | CATGCCACCATTCCC[A/G]GCTACTGTGTGTGTG | 1840 |
rs1674123 | snp | C/T | 0.498652 | 0.0259235 | intron-variant | DTX1 | GRCh38.p7 | 12:113073425 | CTGGGGCAGCCTCAC[C/T]CTGATGCCTGATTTA | 1840 |
rs1732784 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | DTX1 | GRCh38.p7 | 12:113059122 | accaccaacacaacc[A/G]ctaacactgtctcct | 1840 |
rs1732785 | snp | A/G | 0.421684 | 0.181726 | intron-variant | DTX1 | GRCh38.p7 | 12:113058508 | TTTTCAGCATCCTAC[A/G]CTGCAAGGTAGTGAT | 1840 |
rs1732786 | snp | C/T | 0.481009 | 0.0955756 | upstream-variant-2KB, utr-variant-5-prime | DTX1 | GRCh38.p7 | 12:113057841 | AGGTCCAGCCTCTTC[C/T]GTGTTGTCTCTTGGT | 1840 |
rs1732790 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113093924 | TGGCAAGGGTTGGCC[A/G]GGGTCAGGCTGGCAA | 1840 |
rs1732791 | snp | A/G | 0.221439 | 0.248363 | intron-variant | DTX1 | GRCh38.p7 | 12:113092809 | GGTGTAGCTATTTTA[A/G]CATCTCTCAAAGCTT | 1840 |
rs1732792 | snp | C/T | 0.269267 | 0.249256 | intron-variant | DTX1 | GRCh38.p7 | 12:113092787 | TCAAAGCTTGTTAGA[C/T]GTAGCATTATTAATT | 1840 |
rs1732793 | snp | C/T | 0.22263 | 0.248497 | intron-variant | DTX1 | GRCh38.p7 | 12:113091127 | CAGTACCGCACCTGC[C/T]ACTGCCGCCCCTCTC | 1840 |
rs1732794 | snp | C/T | 0.314787 | 0.241459 | intron-variant | DTX1 | GRCh38.p7 | 12:113091019 | CTGCAGCCTGCAGAA[C/T]GGCCTGCCGTCCACA | 1840 |
rs1732795 | snp | A/G | 0.304438 | 0.244001 | intron-variant | DTX1 | GRCh38.p7 | 12:113091010 | GCAGAACGGCCTGCC[A/G]TCCACACGCGGACAC | 1840 |
rs1732796 | snp | C/T | 0.251296 | 0.249997 | intron-variant | DTX1 | GRCh38.p7 | 12:113088540 | tgtatacatgtgcca[C/T]gctggtgtgctgcgc | 1840 |
rs1732797 | snp | C/G | 0.347694 | 0.230122 | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | DTX1, RASAL1 | GRCh38.p7 | 12:113098162 | GAAGGGGTGGGGGCG[C/G]TGAAGCAGTGGCAGA | 1840 |
rs1732800 | snp | G/T | 0.492823 | 0.0594727 | intron-variant | DTX1 | GRCh38.p7 | 12:113074068 | aaatcccgtctctac[G/T]aaaaatacaaaaaaa | 1840 |
rs1732801 | snp | A/G | 0.383439 | 0.21141 | intron-variant | DTX1 | GRCh38.p7 | 12:113074069 | aatcccgtctctacg[A/G]aaaatacaaaaaaaa | 1840 |
rs1732802 | snp | C/T | 0.482384 | 0.0921818 | intron-variant | DTX1 | GRCh38.p7 | 12:113079926 | CTTGAGCCTCAGTTT[C/T]GTCATCTGTCAAATG | 1840 |
rs1732803 | snp | G/T | 0.492287 | 0.0616198 | intron-variant | DTX1 | GRCh38.p7 | 12:113082011 | AAGGAAGTTTTCTCT[G/T]TGGGGGTGCGGATCA | 1840 |
rs1732805 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113060959 | GACTCCCCACAAGGC[C/T]GCCAAGCTGGCAACT | 1840 |
rs1882195 | snp | C/G | | | upstream-variant-2KB | DTX1 | GRCh38.p7 | 12:113056096 | GGGGACCCTGGCCAG[C/G]AGGTGAGATCCTGGA | 1840 |
rs1902953 | snp | C/T | 0.289683 | 0.24683 | | | GRCh38.p7 | 12:113062323 | GCTGCTTTTCTGCTC[C/T]GATAGAGTTGAATAG | 1840 |
rs1902954 | snp | C/T | 0.21695 | 0.247806 | | | GRCh38.p7 | 12:113060504 | TGCACTGGCTGTGCC[C/T]TCTGCCTGGGACACT | 1840 |
rs1902956 | snp | C/T | | | | | GRCh38.p7 | 12:113054848 | agctacttagccttt[C/T]tgagcttcaggaggt | 1840 |
rs2243396 | snp | C/T | 0.331674 | 0.236282 | intron-variant | DTX1 | GRCh38.p7 | 12:113095319 | CTGTACTGTCCCTCT[C/T]TGCAGGGCCCTGAGC | 1840 |
rs2243397 | snp | C/T | 0.328556 | 0.237346 | intron-variant | DTX1 | GRCh38.p7 | 12:113095245 | CCCCAGCCCCCACAC[C/T]CCTCCAACTCCTCCA | 1840 |
rs2246275 | snp | A/G | 0.268452 | 0.249318 | intron-variant | DTX1 | GRCh38.p7 | 12:113092830 | GCCTGAAACCCAACT[A/G]CTAGTGGTGTAGCTA | 1840 |
rs2246844 | snp | C/T | 0.253824 | 0.249971 | intron-variant | DTX1 | GRCh38.p7 | 12:113088534 | catgtgccatgctgg[C/T]gtgctgcgcccatta | 1840 |
rs2254306 | snp | C/G | 0.499437 | 0.0167637 | intron-variant | DTX1 | GRCh38.p7 | 12:113072232 | CCAGGCTTTGTGCCT[C/G]GTGCTCCAAACATAG | 1840 |
rs2254770 | snp | C/G | 0.338523 | 0.233803 | upstream-variant-2KB | DTX1 | GRCh38.p7 | 12:113056518 | ATGTTTAGGAGTCAC[C/G]GGCTTGAATCTTTGT | 1840 |
rs2264886 | snp | C/T | 0.113685 | 0.209567 | intron-variant | DTX1 | GRCh38.p7 | 12:113088657 | ttaccttactgaatt[C/T]ttttttcatagcact | 1840 |
rs2264887 | snp | C/T | 0.412249 | 0.190198 | intron-variant | DTX1 | GRCh38.p7 | 12:113080618 | TGGAATGGAATGGAA[C/T]GGAATGGAAAACAGA | 1840 |
rs2279044 | snp | C/T | 0.00119737 | 0.0244387 | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | DTX1, RASAL1 | GRCh38.p7 | 12:113098092 | GGCTGCAGTCAGCCC[C/T]GTTGGGGAGTGATGG | 1840 |
rs2305905 | snp | A/G | 0.000101329 | 0.00711718 | intron-variant | DTX1 | GRCh38.p7 | 12:113094989 | GAGTGGGCAGGGAAC[A/G]GAGTGGGGTTTGGGG | 1840 |
rs2384077 | snp | A/G | 0.413748 | 0.188909 | intron-variant | DTX1 | GRCh38.p7 | 12:113066691 | ATTCATTCATCAGGA[A/G]TTTCATGAGCACCTA | 1840 |
rs2464289 | snp | A/G | 0.27008 | 0.249192 | intron-variant | DTX1 | GRCh38.p7 | 12:113090407 | GGGCACCCTGCGGGG[A/G]GGCCCCAGGAAGAGG | 1840 |
rs2464290 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113081845 | TCCAGAAGGGAGCCT[C/T]TATCCCCCGGTGGTC | 1840 |
rs2468356 | snp | G/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113091400 | CCCCATCCGTCTACT[G/T]GGGAACATACCGCAC | 1840 |
rs2701622 | snp | C/T | 0.35574 | 0.226537 | intron-variant | DTX1 | GRCh38.p7 | 12:113095541 | GTGGTCGTTACTGTT[C/T]GGGTGCTGCTTTTGG | 1840 |
rs2701623 | snp | A/G | 0.457388 | 0.139608 | intron-variant | DTX1 | GRCh38.p7 | 12:113084969 | CCAGTcccatttcac[A/G]gatgcaaaaactgaa | 1840 |
rs2701624 | snp | A/C | 0.499396 | 0.0173617 | intron-variant | DTX1 | GRCh38.p7 | 12:113072847 | GCGTGGTGGTACGTG[A/C]CTGTAATCCCAGTTA | 1840 |
rs2731303 | snp | G/T | 0.491525 | 0.0645418 | intron-variant | DTX1 | GRCh38.p7 | 12:113085700 | TCAATAAATATGAAT[G/T]AATTAATTAAAAAAC | 1840 |
rs3038192 | in-del | -/GGTAG | | | intron-variant | DTX1 | GRCh38.p7 | 12:113074509 | agggggaagggtagg[-/GGTAG]acaatgccagaggag | 1840 |
rs3038193 | in-del | -/TTTTTTT | | | intron-variant | DTX1 | GRCh38.p7 | 12:113079537 | ttttttttttttttt[-/TTTTTTT]gagatacagtttcac | 1840 |
rs3178412 | snp | A/C | 0 | 0 | missense, utr-variant-3-prime, nc-transcript-variant | DTX1, RASAL1 | GRCh38.p7 | 12:113096917 | CAGCCCAGGGCGTAT[A/C]CGAGGCTGCAGCCAA | 1840 |
rs3180323 | snp | C/T | 0 | 0 | utr-variant-3-prime, nc-transcript-variant | DTX1, RASAL1 | GRCh38.p7 | 12:113096944 | CCAAGGCTTGAGGCC[C/T]AAGGCTGCCCACCTT | 1840 |
rs3214864 | in-del | -/A | | | utr-variant-3-prime, nc-transcript-variant | DTX1, RASAL1 | GRCh38.p7 | 12:113097547 | CAGTTCTACAAAAAA[-/A]TGGCCAGCACGAGCG | 1840 |
rs3217697 | in-del | -/AG | 0.22263 | 0.248497 | intron-variant | DTX1 | GRCh38.p7 | 12:113093040 | GTAACTGCAGTTGGC[-/AG]AGAGAGGTACAAAGA | 1840 |
rs3741985 | snp | C/G | 0.480853 | 0.0959518 | upstream-variant-2KB, utr-variant-5-prime | DTX1 | GRCh38.p7 | 12:113057821 | TGTCTCTTGGTCCCT[C/G]TTCCCCGCCAGACAG | 1840 |
rs3741986 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | DTX1 | GRCh38.p7 | 12:113093976 | CCCGAAGGCTTGGCT[C/T]AGAACTGGGTCAGGG | 1840 |
rs3809163 | snp | A/G | 0.169435 | 0.236663 | intron-variant | DTX1 | GRCh38.p7 | 12:113066062 | CTGGGTGGGCTCATG[A/G]GGGTGACTATCTAAG | 1840 |
rs3825200 | snp | A/G | 0.469346 | 0.119947 | intron-variant | DTX1 | GRCh38.p7 | 12:113066092 | CTGCTGGGGGTGTCT[A/G]TGTCAACCCAGAGGC | 1840 |
rs3839970 | in-del | -/CTGC | | | intron-variant | DTX1 | GRCh38.p7 | 12:113089522 | GCGACCGCTGCCTGC[-/CTGC]GGGCCTCCCGGAAGG | 1840 |
rs3847955 | snp | C/T | 0.412416 | 0.190055 | intron-variant | DTX1 | GRCh38.p7 | 12:113087422 | CCCCCGGGCTTGCAG[C/T]GATGTCCTTCAAGTC | 1840 |
rs4561264 | snp | A/G | 0.147321 | 0.227941 | intron-variant | DTX1 | GRCh38.p7 | 12:113081950 | TTGGTGCTGCCATCA[A/G]TGGGGAGCTATAGAG | 1840 |
rs4767061 | snp | C/T | 0.0368353 | 0.130617 | upstream-variant-2KB | DTX1 | GRCh38.p7 | 12:113055242 | TGCTAAATCACCATG[C/T]GACCTTGAGCCAATC | 1840 |
rs4767062 | snp | A/C | 0.120326 | 0.21374 | intron-variant | DTX1 | GRCh38.p7 | 12:113076984 | CAGGGCCTGTGATAA[A/C]CCCCACTTCAGTGTC | 1840 |
rs7294709 | snp | C/T | 0.150333 | 0.229274 | intron-variant | DTX1 | GRCh38.p7 | 12:113082877 | gctgggaattatagg[C/T]gtgagccacagcgac | 1840 |
rs7296817 | snp | A/C | 0.0279526 | 0.114869 | intron-variant | DTX1 | GRCh38.p7 | 12:113079330 | GATAATGATGGTCCG[A/C]GATCACCAAAGCTCA | 1840 |
rs7298895 | snp | C/T | 0.345925 | 0.230864 | intron-variant | DTX1 | GRCh38.p7 | 12:113064105 | AGGGACAGCCTGCAC[C/T]ACCCTGGAGGCCTCC | 1840 |
rs7305270 | snp | A/G | 0.0948562 | 0.196037 | upstream-variant-2KB | DTX1 | GRCh38.p7 | 12:113055803 | AGGCCACTGACCCCC[A/G]TCAGCCACCCAGGCT | 1840 |
rs7306576 | snp | C/T | 0.0948562 | 0.196037 | upstream-variant-2KB | DTX1 | GRCh38.p7 | 12:113056111 | CCTGGCCAGGGTCCC[C/T]TCCCCTGGTCCCACC | 1840 |
rs7308220 | snp | G/T | 0.00259286 | 0.0359125 | intron-variant | DTX1 | GRCh38.p7 | 12:113094121 | AGGGGATGGGGGGGC[G/T]GGGGGAGGGCCCTGG | 1840 |
rs7954586 | snp | C/G | 0.0436148 | 0.141086 | intron-variant | DTX1 | GRCh38.p7 | 12:113093533 | ACTGCGCCCCCTAAC[C/G]CCCAGGGATGACCGG | 1840 |
rs7958787 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113059792 | caaccaatatgttag[C/T]caccaaccacatgtg | 1840 |
rs7960088 | snp | A/G | 0.161924 | 0.233971 | intron-variant | DTX1 | GRCh38.p7 | 12:113075968 | attctagcgaggggg[A/G]gacagacagaaacca | 1840 |
rs7976615 | snp | C/G | 0.155656 | 0.231515 | intron-variant | DTX1 | GRCh38.p7 | 12:113079766 | atttcaccatgtttc[C/G]caggcttgtcttgaa | 1840 |
rs10610484 | in-del | -/CA | 0.495483 | 0.0473088 | intron-variant | DTX1 | GRCh38.p7 | 12:113084996 | CTGGCAACACAGGCC[-/CA]CATAGTCCATCATGA | 1840 |
rs10688520 | in-del | -/AA | 0.465052 | 0.127485 | intron-variant | DTX1 | GRCh38.p7 | 12:113087126 | GGACCGGGAGGGTTG[-/AA]GAAGAGTGACCCCCG | 1840 |
rs10744794 | snp | C/T | 0.4983 | 0.0291038 | intron-variant | DTX1 | GRCh38.p7 | 12:113071823 | GGGTGCAGGGCCCAG[C/T]GGGGAGGACAGCAGC | 1840 |
rs10850126 | snp | G/T | 0.0425829 | 0.139564 | upstream-variant-2KB | DTX1 | GRCh38.p7 | 12:113055173 | acatttaaTCAGACC[G/T]TAAATAGCATTCGAC | 1840 |
rs10850127 | snp | C/T | 0.196149 | 0.244131 | intron-variant | DTX1 | GRCh38.p7 | 12:113075140 | GCTACAGCTGGCAAA[C/T]GCAGCAGTCTTCTAT | 1840 |
rs10850128 | snp | A/C/T | 0.492922 | 0.222896 | intron-variant | DTX1 | GRCh38.p7 | 12:113077110 | GCTCTCCCGCCCCTA[A/C/T]GCCCAATCTACTGAC | 1840 |
rs11066481 | snp | C/G | | | upstream-variant-2KB, utr-variant-5-prime | DTX1 | GRCh38.p7 | 12:113056741 | TCCCACCCGCGAGAT[C/G]CCGGCGGCCGCCAGC | 1840 |
rs11066482 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | DTX1 | GRCh38.p7 | 12:113062999 | ATGTTAGATCAATCA[C/T]GGTGGTGTCCCAGGC | 1840 |
rs11066483 | snp | G/T | 0.474272 | 0.110462 | intron-variant | DTX1 | GRCh38.p7 | 12:113063594 | GCTGAGGCCGAGGGA[G/T]GCCAGCTGGGGACCA | 1840 |
rs11066484 | snp | G/T | 0.0107246 | 0.0724382 | intron-variant | DTX1 | GRCh38.p7 | 12:113064237 | GTAGGGGCAGGGAGC[G/T]GCCCATCTCTGGTAG | 1840 |
rs11066485 | snp | A/C | | | intron-variant | DTX1 | GRCh38.p7 | 12:113067765 | GGCCATTTGAggtgg[A/C]tcatgcctggaatcc | 1840 |
rs11066486 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113068330 | CAGACACCTCCGCAC[C/T]TAGTGAGCTATGTGC | 1840 |
rs11066487 | snp | C/G | 0.0111196 | 0.0737302 | intron-variant | DTX1 | GRCh38.p7 | 12:113071567 | CAGCCTGAGGCCCAG[C/G]CTCTTTCCCAGGCTG | 1840 |
rs11066488 | snp | C/T | 0.356811 | 0.226034 | intron-variant | DTX1 | GRCh38.p7 | 12:113074086 | AAATACAAAAAAAAT[C/T]AGCTGGGTGACACAT | 1840 |
rs11066489 | snp | C/G | 0.0505692 | 0.150756 | intron-variant | DTX1 | GRCh38.p7 | 12:113075964 | TTACATTCTAGCGAG[C/G]GGGGGACAGACAGAA | 1840 |
rs11066490 | snp | A/G | 0.0513262 | 0.151752 | intron-variant | DTX1 | GRCh38.p7 | 12:113078641 | CTTCTCAGGGTCACC[A/G]GGGAAGGGTAGACAT | 1840 |
rs11066491 | snp | C/G | 0.153 | 0.230415 | intron-variant | DTX1 | GRCh38.p7 | 12:113087182 | GAGCCTCCAATACCA[C/G]TCACACCTCAAAATG | 1840 |
rs11325819 | in-del | -/G | 0.316 | 0.241131 | utr-variant-3-prime, nc-transcript-variant | DTX1, RASAL1 | GRCh38.p7 | 12:113097545 | AGCAGTTCTACAAAA[-/G]AATGGCCAGCACGAG | 1840 |
rs11372823 | in-del | -/A | 0.453209 | 0.145623 | intron-variant | DTX1 | GRCh38.p7 | 12:113092326 | TTAAAAAAAAAAAAA[-/A]GGTACCATATTGTCC | 1840 |
rs11545319 | snp | A/G | 0.120674 | 0.21395 | utr-variant-3-prime, nc-transcript-variant | DTX1, RASAL1 | GRCh38.p7 | 12:113097161 | GGTAGGGAGGTTTCC[A/G]GTACTCTCTGCTTGG | 1840 |
rs11609327 | snp | A/C | | | intron-variant | DTX1 | GRCh38.p7 | 12:113066984 | CTCTGGGCTCCTTCC[A/C]TCATCCCTCTGGAGC | 1840 |
rs11611469 | snp | G/T | 0.175254 | 0.238565 | intron-variant | DTX1 | GRCh38.p7 | 12:113070178 | GCTAAACACACTCTT[G/T]CGCTTGAATGAGCTA | 1840 |
rs11829749 | snp | A/G | 0.030278 | 0.119257 | intron-variant, downstream-variant-500B | DTX1, RASAL1 | GRCh38.p7 | 12:113096397 | gtgagctctggttgc[A/G]ctgctgcactccagc | 1840 |
rs11835093 | snp | A/C | 0.349233 | 0.229462 | intron-variant | DTX1 | GRCh38.p7 | 12:113063562 | GGCAGCCTCCTGCCC[A/C]TTCTGCTGATGGGAT | 1840 |
rs12299862 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | DTX1 | GRCh38.p7 | 12:113061141 | CCAGAAGTTCAGCTC[C/T]GGTCACTTCCCCTCT | 1840 |
rs12300335 | snp | G/T | 0.0611083 | 0.163768 | intron-variant | DTX1 | GRCh38.p7 | 12:113064425 | GCTTCTCAGTACCAG[G/T]TCCTGGGCTGGGTCT | 1840 |
rs12303264 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | DTX1 | GRCh38.p7 | 12:113068717 | gagcagaggagtgac[A/G]cagtccagccttgag | 1840 |
rs12311239 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | DTX1 | GRCh38.p7 | 12:113069589 | GAAACAGAACACTGC[A/G]GGATTATTGATCATG | 1840 |
rs12318088 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | DTX1 | GRCh38.p7 | 12:113090695 | TGCTCCAGACCTCTC[C/T]ACAGCCCTCAGAGGG | 1840 |
rs12422420 | snp | C/T | 0.201012 | 0.245153 | intron-variant | DTX1 | GRCh38.p7 | 12:113094739 | GCAGTGCTGACCCAG[C/T]AGGTGCCCTGCCCTC | 1840 |
rs12426056 | snp | C/T | 0.196753 | 0.244264 | synonymous-codon | DTX1 | GRCh38.p7 | 12:113095080 | CTGCAAGGCCATCTA[C/T]GGGGAGAAGACGGGT | 1840 |
rs12427377 | snp | A/G | 0.202614 | 0.245468 | synonymous-codon | DTX1 | GRCh38.p7 | 12:113094812 | CATCTGCATGGAGCG[A/G]CTGGTCACAGCATCA | 1840 |
rs12813843 | snp | A/C | 0.00888871 | 0.0660708 | upstream-variant-2KB, intron-variant | DTX1 | GRCh38.p7 | 12:113057251 | CCCCAGGCGGAGAGT[A/C]TCGGAAAACCGCGCC | 1840 |
rs12813999 | snp | C/T | | | upstream-variant-2KB, intron-variant | DTX1 | GRCh38.p7 | 12:113057284 | CGGCCCCTGCCTTCC[C/T]TCCAGGCCTGCCCCA | 1840 |
rs12815873 | snp | A/C | 0.0501905 | 0.150254 | intron-variant | DTX1 | GRCh38.p7 | 12:113074780 | gggagcagtggtcag[A/C]tgtggatgtgtttga | 1840 |
rs12817870 | snp | C/T | 0.181659 | 0.240478 | intron-variant | DTX1 | GRCh38.p7 | 12:113078640 | CCTTCTCAGGGTCAC[C/T]GGGGAAGGGTAGACA | 1840 |
rs12819091 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113072697 | ACCTGAGAGAttttc[C/T]ttttttttttttttt | 1840 |
rs12819639 | snp | A/T | | | upstream-variant-2KB, intron-variant | DTX1 | GRCh38.p7 | 12:113057285 | GGCCCCTGCCTTCCC[A/T]CCAGGCCTGCCCCAA | 1840 |
rs12820500 | snp | A/G | 0.0599851 | 0.162463 | intron-variant | DTX1 | GRCh38.p7 | 12:113087998 | GCCCAGGCCTGAGCC[A/G]GCTCCAGGATCCAGG | 1840 |
rs12821868 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113084958 | cctctctggtcttca[A/G]tttttgcatctgtga | 1840 |
rs12822441 | snp | A/G | 0.161596 | 0.233848 | intron-variant | DTX1 | GRCh38.p7 | 12:113063628 | AAAGATGCCATACCC[A/G]AGGCTGCAAGCCTGG | 1840 |
rs12824555 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113079612 | cactgactgcaactt[C/T]tgcctccagggttca | 1840 |
rs12825164 | snp | C/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113079854 | atgagccaccatgcc[C/G]ggcccccttcttgac | 1840 |
rs12825174 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113079875 | ccttcttgaccactt[C/T]tgagctgggagacct | 1840 |
rs12825685 | snp | A/C | | | intron-variant | DTX1 | GRCh38.p7 | 12:113079756 | tggagatgggatttc[A/C]ccatgtttcccaggc | 1840 |
rs12829035 | snp | G/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113084952 | catcttcctctctgg[G/T]cttcagtttttgcat | 1840 |
rs12829207 | snp | G/T | 0 | 0 | intron-variant | DTX1 | GRCh38.p7 | 12:113084976 | tttgcatctgtgaaa[G/T]gggACTGGCAACACA | 1840 |
rs12831224 | snp | A/G | 0.0513262 | 0.151752 | intron-variant | DTX1 | GRCh38.p7 | 12:113093364 | CTGGGCCCAGGACAC[A/G]GGGCGGGCGTGGCCC | 1840 |
rs16942518 | snp | C/G | 0.18325 | 0.240924 | intron-variant | DTX1 | GRCh38.p7 | 12:113073012 | GCACCTGGCTCGACC[C/G]GAGAGACTTCTGAGT | 1840 |
rs17854541 | snp | C/T | | | synonymous-codon | DTX1 | GRCh38.p7 | 12:113094794 | CCACCTGCAGGACTG[C/T]ACCATCTGCATGGAG | 1840 |
rs28453325 | snp | A/C | | | intron-variant | DTX1 | GRCh38.p7 | 12:113067880 | CCACCAAATAAAAAC[A/C]AAAAAAAAAATAGCT | 1840 |
rs34020980 | in-del | -/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113060786 | TTCTGTTTTCTCCTA[-/G]GGGTAGAGGGCAGGG | 1840 |
rs34145403 | snp | A/G | 0.354881 | 0.226936 | intron-variant | DTX1 | GRCh38.p7 | 12:113059027 | AGTGTTGGTTTGTGG[A/G]GTGGAGTCGTGCTGG | 1840 |
rs34191594 | in-del | -/T | 0.428786 | 0.174744 | intron-variant | DTX1 | GRCh38.p7 | 12:113061699 | AAAAGATCTTAAATC[-/T]TTTTTTTTTCTTCTT | 1840 |
rs34399361 | snp | A/C | 0.375 | 0.216506 | utr-variant-5-prime | DTX1 | GRCh38.p7 | 12:113057886 | TGCCTCACTCCCTAC[A/C]TGAGCCAGCCGAGGG | 1840 |
rs34456508 | in-del | -/G | 0.375399 | 0.216275 | intron-variant | DTX1 | GRCh38.p7 | 12:113080091 | TAATTTTCCAGGGAT[-/G]CATCACAGCCACTAC | 1840 |
rs34563026 | in-del | -/C | | | intron-variant | DTX1 | GRCh38.p7 | 12:113066719 | CTACTGTGTGCCAGG[-/C]ACTGTCCGGGCACTA | 1840 |
rs34596650 | in-del | -/C | | | intron-variant | DTX1 | GRCh38.p7 | 12:113072695 | GACCTGAGAGATTTT[-/C]CTTTTTTTTTTTTTT | 1840 |
rs34629496 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | DTX1 | GRCh38.p7 | 12:113092142 | GTTTTGTGGTTTCCT[C/T]TCTAAGATGGAGAGA | 1840 |
rs34859653 | snp | C/G | 0.162253 | 0.234095 | intron-variant | DTX1 | GRCh38.p7 | 12:113063323 | GCCACATCTTCCCTG[C/G]GGGGTCATTTACATC | 1840 |
rs34865485 | in-del | -/GTT | | | intron-variant | DTX1 | GRCh38.p7 | 12:113088851 | CTCCTCAAAAGTTTT[-/GTT]GTTGTTGTTGTTGTT | 1840 |
rs35079582 | in-del | -/C | | | intron-variant | DTX1 | GRCh38.p7 | 12:113095927 | AAAAAACAGGCAGGG[-/C]CCGGGTGTGGTGGCT | 1840 |
rs35096714 | snp | A/G | 0.161924 | 0.233971 | intron-variant | DTX1 | GRCh38.p7 | 12:113063739 | TTCCCTGGAAACCTT[A/G]GGCTTCACTCAGCCC | 1840 |
rs35204770 | in-del | -/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113060427 | GCCCAGAGGTACTCA[-/G]GGGAAGGCTAGCCTG | 1840 |
rs35413793 | in-del | -/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113087746 | GTGAGGTATCCTGAA[-/G]GGGGCCAAGGCCAAT | 1840 |
rs35422556 | in-del | -/ACAC | | | intron-variant | DTX1 | GRCh38.p7 | 12:113062033 | AATATTATATTTCAT[-/ACAC]ACACACACACACACA | 1840 |
rs35450040 | snp | C/G | 0.17332 | 0.23795 | intron-variant | DTX1 | GRCh38.p7 | 12:113070512 | GAGGAACCGTTTAGA[C/G]GCTGAGGGACCAGCA | 1840 |
rs35457626 | in-del | -/A | 0.455977 | 0.141681 | intron-variant | DTX1 | GRCh38.p7 | 12:113086269 | GAAAAAAAAAAAAAA[-/A]GCAAAAGAACTGGGG | 1840 |
rs35462060 | in-del | -/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113066717 | ACCTACTGTGTGCCA[-/G]GCACTGTCCGGGCAC | 1840 |
rs35476554 | snp | C/T | 0.213333 | 0.247296 | intron-variant | DTX1 | GRCh38.p7 | 12:113078385 | CCCAAGATCAGACAG[C/T]TCACAAGTGATGGGG | 1840 |
rs35516980 | in-del | -/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113068006 | TGGCACCACTGCAAT[-/G]CCACCCTGGGCAACA | 1840 |
rs35606511 | in-del | -/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113091576 | ATGCATGTGTGTATA[-/T]TTTGGATCTGTGGAT | 1840 |
rs35618571 | in-del | -/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113072420 | AGGAGATGAGCACAT[-/G]GGAGGGCTTTGCTGG | 1840 |
rs35694234 | in-del | -/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113065879 | CAGTAGGCAATGGGG[-/T]TTGAGGTCCCTAACT | 1840 |
rs35711481 | in-del | -/G | | | upstream-variant-2KB | DTX1 | GRCh38.p7 | 12:113055688 | CCAGAGCTGGATTCT[-/G]GGGAAAGCACCCCTG | 1840 |
rs35800593 | snp | A/C | 0.163236 | 0.234461 | intron-variant | DTX1 | GRCh38.p7 | 12:113068091 | TTTAAATGTAAATAG[A/C]ATGTGAACCAGAACA | 1840 |
rs35908809 | snp | C/T | 0.0711601 | 0.174689 | intron-variant | DTX1 | GRCh38.p7 | 12:113094008 | ACAGACTCTGGGTAC[C/T]CTCAAACCCACCCCG | 1840 |
rs35924122 | in-del | -/C | | | intron-variant | DTX1 | GRCh38.p7 | 12:113079246 | GGTTTGGACTGTGGT[-/C]CCCCAAGAGGAAGAG | 1840 |
rs36001651 | in-del | -/C | | | intron-variant | DTX1 | GRCh38.p7 | 12:113091885 | CTGGATTTCAGAACA[-/C]CCCTCTTCATCAGAA | 1840 |
rs36020415 | snp | C/G | 0.0513262 | 0.151752 | intron-variant | DTX1 | GRCh38.p7 | 12:113093760 | GCCTTGACCACAACT[C/G]TGTGACCCCTGGTCT | 1840 |
rs36092635 | in-del | -/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113071155 | GTCTCTGACAGTCTC[-/T]TTTGATCATGTATGT | 1840 |
rs55683465 | snp | A/C | 0.0551013 | 0.156571 | intron-variant | DTX1 | GRCh38.p7 | 12:113066102 | TGACACAGACACCCC[A/C]AGCAGCCCCTAGCTG | 1840 |
rs55734931 | snp | C/T | 0.173643 | 0.238054 | intron-variant | DTX1 | GRCh38.p7 | 12:113084080 | GCCCAGAGAGGGGGA[C/T]TGGCTCATCTAGGGT | 1840 |
rs55782134 | snp | A/T | 0.0126979 | 0.078662 | intron-variant | DTX1 | GRCh38.p7 | 12:113075818 | AAGTGTGAATGAATT[A/T]AAAAAAAAAGAATCC | 1840 |
rs55853221 | in-del | -/A/AAA | | | intron-variant | DTX1 | GRCh38.p7 | 12:113080989 | AAAAAAAAAAAAAAA[-/A/AAA]TTGCTCCATGAATGT | 1840 |
rs55875448 | snp | A/G | 0.095934 | 0.196885 | intron-variant | DTX1 | GRCh38.p7 | 12:113064124 | CTGGAGGCCTCCAGG[A/G]CTCAGCTCCTGGTTA | 1840 |
rs55888393 | in-del | -/TGGAATGGAA | | | intron-variant | DTX1 | GRCh38.p7 | 12:113080627 | TGGAACGGAATGGAA[-/TGGAATGGAA]AACAGAATAGAACTA | 1840 |
rs55918139 | in-del | -/CT | 0.172997 | 0.237846 | intron-variant | DTX1 | GRCh38.p7 | 12:113073874 | AAGCAGACAAGATCC[-/CT]GACTTTGCAGCTGAC | 1840 |
rs55999512 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | DTX1 | GRCh38.p7 | 12:113073700 | AGCCCTGAGTAGGGA[C/T]ACACCAGTGTGGAAC | 1840 |
rs56194115 | in-del | -/AAAA | 0 | 0 | intron-variant, downstream-variant-500B | DTX1, RASAL1 | GRCh38.p7 | 12:113096459 | AAAAAAAAAAAAAAA[-/AAAA]GAAAAAGAAAAAAAA | 1840 |
rs56358913 | in-del | -/A | 0.415727 | 0.187175 | intron-variant | DTX1 | GRCh38.p7 | 12:113067880 | CCACCAAATAAAAAC[-/A]AAAAAAAAAATAGCT | 1840 |
rs56382675 | in-del | -/AA | | | intron-variant | DTX1 | GRCh38.p7 | 12:113076476 | AAAAAAAAAAAAAAA[-/AA]GTGGGGCCGGTCATG | 1840 |
rs57447229 | snp | C/G | 0.0569829 | 0.158885 | intron-variant | DTX1 | GRCh38.p7 | 12:113067925 | ACACCTGTGATCCCA[C/G]CTACTCAGGAGGCTG | 1840 |
rs57749572 | snp | C/T | 0.159951 | 0.233219 | intron-variant | DTX1 | GRCh38.p7 | 12:113059004 | ACTGGTATCCTATAC[C/T]GGCTCCAAGTGTTGG | 1840 |
rs57893303 | snp | C/T | 0.107694 | 0.205546 | intron-variant | DTX1 | GRCh38.p7 | 12:113060140 | ATTGATGGTACAGAT[C/T]AGTACATCTATGTTT | 1840 |
rs58045905 | snp | A/G | 0.0678174 | 0.1712 | intron-variant | DTX1 | GRCh38.p7 | 12:113063518 | GGTATCTCCCATGTC[A/G]CTCTCCATGTGCTGC | 1840 |
rs58273997 | snp | G/T | 0.0142736 | 0.0832652 | intron-variant | DTX1 | GRCh38.p7 | 12:113060239 | TTTATTGATCTCTGC[G/T]GTGTGTCAATTTCTG | 1840 |
rs58489579 | snp | A/C | 0.0944967 | 0.195752 | intron-variant | DTX1 | GRCh38.p7 | 12:113061259 | GAGCCTGCCAGGAAC[A/C]CCCTCCCACCCCAAC | 1840 |
rs58716967 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | DTX1 | GRCh38.p7 | 12:113067928 | CCTGTGATCCCAGCT[A/G]CTCAGGAGGCTGAGG | 1840 |
rs58720511 | snp | A/T | 0.126564 | 0.217402 | intron-variant | DTX1 | GRCh38.p7 | 12:113086700 | TTATGCTTTTATTTT[A/T]AAAAAATCCACATTT | 1840 |
rs58836946 | snp | G/T | 0.00953873 | 0.0683987 | intron-variant | DTX1 | GRCh38.p7 | 12:113086547 | GACTGTTTTAACAGG[G/T]TCACTCTGAATGCTG | 1840 |
rs59863042 | snp | C/G | | | upstream-variant-2KB, intron-variant | DTX1 | GRCh38.p7 | 12:113057198 | GCAGGGCGAGGGCCC[C/G]GGGGGAAGGGAAGGC | 1840 |
rs60013451 | snp | A/G | 0.0966517 | 0.197444 | intron-variant | DTX1 | GRCh38.p7 | 12:113064386 | GAAACTAAATTCATC[A/G]CTCGTATTTGGTAGT | 1840 |
rs60200260 | snp | G/T | 0.159951 | 0.233219 | intron-variant | DTX1 | GRCh38.p7 | 12:113059005 | CTGGTATCCTATACT[G/T]GCTCCAAGTGTTGGT | 1840 |
rs60265483 | in-del | -/TAGGCCGGGTGTG | | | intron-variant | DTX1 | GRCh38.p7 | 12:113066245 | GAATCATGGGGTGTG[-/TAGGCCGGGTGTG]GTGGCTCACATCTAT | 1840 |
rs60638692 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | DTX1 | GRCh38.p7 | 12:113072044 | CTGATGTTGAGAATC[C/T]TCCTCCTGGCCTGAG | 1840 |
rs60642403 | in-del | -/T/TT | 0 | 0 | intron-variant | DTX1 | GRCh38.p7 | 12:113072721 | TTTTTTTTTTTTTTT[-/T/TT]GAGACAGAGTCTTGC | 1840 |
rs61758446 | snp | C/T | 0.044286 | 0.142064 | synonymous-codon | DTX1 | GRCh38.p7 | 12:113095345 | TGAGCACCCCAACCC[C/T]GGGAAGAAGTTCACC | 1840 |
rs61758447 | snp | C/T | 0.0331521 | 0.124406 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant | DTX1, RASAL1 | GRCh38.p7 | 12:113096828 | GATCCACCACAAGAC[C/T]GAGTTTGGATCCAAC | 1840 |
rs61942305 | snp | A/C | 0.0310518 | 0.120672 | intron-variant | DTX1 | GRCh38.p7 | 12:113061375 | GCCTCCTCACCAGAT[A/C]TGTGAGGGTTTTTCC | 1840 |
rs61942306 | snp | C/T | 0.5 | 0 | intron-variant | DTX1 | GRCh38.p7 | 12:113074738 | GGAGAGATAACATGG[C/T]GGGGACTGGGTGGTG | 1840 |
rs61942307 | snp | C/T | 0.483491 | 0.0893421 | intron-variant | DTX1 | GRCh38.p7 | 12:113077143 | CGCGCCCCTGCCCAC[C/T]TCTCGCCCCAGTGCT | 1840 |
rs61942308 | snp | A/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113081819 | TAGGAATGAATCCAG[A/T]AGGTTCTGGAGACCA | 1840 |
rs61942309 | snp | A/T | 0.0678174 | 0.1712 | intron-variant | DTX1 | GRCh38.p7 | 12:113085214 | GCCACCAACCCGGCT[A/T]ATTTTTTATATTTTT | 1840 |
rs61942310 | snp | A/G | 0.128288 | 0.218372 | intron-variant | DTX1 | GRCh38.p7 | 12:113086759 | CATTTCAGGGGTTTG[A/G]AAATGTTAAAGTACT | 1840 |
rs66469391 | in-del | AGCTAC/GGCTACTGTG | 0.5 | 0 | intron-variant | DTX1 | GRCh38.p7 | 12:113079692 | CATGCCACCATTCCC[AGCTAC/GGCTACTGTG]TGTGTGTGTGTGTGT | 1840 |
rs68176148 | snp | A/G | 0.162253 | 0.234095 | intron-variant | DTX1 | GRCh38.p7 | 12:113061986 | GCTGGGATTACAAGC[A/G]TGAGCCACTGTGCCT | 1840 |
rs71086139 | in-del | -/TG | 0 | 0 | intron-variant | DTX1 | GRCh38.p7 | 12:113079714 | GTGTGTGTGTGTGTG[-/TG]TGTGTGTGTGTGTGT | 1840 |
rs71086142 | in-del | -/T | 0 | 0 | intron-variant | DTX1 | GRCh38.p7 | 12:113094248 | TGAATAGAAATACTT[-/T]ACGTTTAATAGACTC | 1840 |
rs71445593 | in-del | -/C | 0.5 | 0 | intron-variant | DTX1 | GRCh38.p7 | 12:113065493 | CCCTCGCAGCCCTCT[-/C]CCCTCTCCTTCTCCT | 1840 |
rs71445594 | in-del | -/GC | 0.493154 | 0.0581045 | intron-variant | DTX1 | GRCh38.p7 | 12:113066718 | CCTACTGTGTGCCAG[-/GC]ACTGTCCGGGCACTA | 1840 |
rs71445595 | in-del | -/T | 0.5 | 0 | intron-variant | DTX1 | GRCh38.p7 | 12:113072696 | ACCTGAGAGATTTTC[-/T]TTTTTTTTTTTTTTT | 1840 |
rs71445596 | in-del | -/A | 0.367987 | 0.220406 | intron-variant | DTX1 | GRCh38.p7 | 12:113078120 | GGTAAGACGGGGCCC[-/A]GGGGGAGGGGGCCTC | 1840 |
rs71445597 | in-del | -/A/AAA | 0.5 | 0 | intron-variant | DTX1 | GRCh38.p7 | 12:113080974 | GCAAGACACTGTCTC[-/A/AAA]AAAAAAAAAAAAAAA | 1840 |
rs71445598 | in-del | -/T | 0.0429648 | 0.14013 | intron-variant | DTX1 | GRCh38.p7 | 12:113094246 | GATGAATAGAAATAC[-/T]TTACGTTTAATAGAC | 1840 |
rs71465878 | snp | C/G | 0.5 | 0 | intron-variant | DTX1 | GRCh38.p7 | 12:113065379 | GCTGGGTGCGCACGG[C/G]CCTTCCCAGGCTCGC | 1840 |
rs71784082 | in-del | -/AA/AG | | | intron-variant | DTX1 | GRCh38.p7 | 12:113087127 | ACCGGGAGGGTTGAA[-/AA/AG]GAGTGACCCCCGCAG | 1840 |
rs73205279 | snp | C/T | 0.267091 | 0.249415 | intron-variant | DTX1 | GRCh38.p7 | 12:113070504 | AGCCCAGAGAGGAAC[C/T]GTTTAGAGGCTGAGG | 1840 |
rs73205282 | snp | C/G | 0.127944 | 0.218179 | intron-variant | DTX1 | GRCh38.p7 | 12:113077061 | TGCTGGTTTCCTACC[C/G]CAGGCTATCTTGGCA | 1840 |
rs73205286 | snp | A/G | 0.145642 | 0.227177 | intron-variant | DTX1 | GRCh38.p7 | 12:113079452 | GAACTAGGTGGCCCT[A/G]TTCACCTTTTGTCCC | 1840 |
rs73205289 | snp | C/T | 0.150333 | 0.229274 | intron-variant | DTX1 | GRCh38.p7 | 12:113082671 | CGCAATCACAGCTCC[C/T]GGCAGCCTGAAACTT | 1840 |
rs73205291 | snp | C/T | 0.176861 | 0.239062 | intron-variant | DTX1 | GRCh38.p7 | 12:113083052 | TCTGAGGCCTCTCTC[C/T]TGGGCTTGTAGATTG | 1840 |
rs73205292 | snp | C/T | 0.150333 | 0.229274 | intron-variant | DTX1 | GRCh38.p7 | 12:113083074 | TGTAGATTGCATCTT[C/T]TACCTGTGTCCTCAT | 1840 |
rs73205293 | snp | A/G | 0.179105 | 0.239737 | intron-variant | DTX1 | GRCh38.p7 | 12:113083152 | AAGGACATCAGTCCT[A/G]TTGGATTAGGGCCCA | 1840 |
rs73205294 | snp | G/T | 0.150333 | 0.229274 | intron-variant | DTX1 | GRCh38.p7 | 12:113083272 | CAACACATGACTTCT[G/T]TGGGGCACAGTTCAG | 1840 |
rs73205298 | snp | C/G | 0.105569 | 0.204058 | intron-variant | DTX1 | GRCh38.p7 | 12:113093906 | TCTGACCCTGGCCAA[C/G]CCTTGCCAGCCTGAC | 1840 |
rs73205299 | snp | C/T | 0.116488 | 0.211364 | utr-variant-3-prime, nc-transcript-variant | DTX1, RASAL1 | GRCh38.p7 | 12:113097589 | GTCCTGATTTTGTGT[C/T]TGTGCCTCTTCATCT | 1840 |
rs73205300 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | DTX1, RASAL1 | GRCh38.p7 | 12:113097905 | GCAACTCACCAGCTC[C/T]GCCTCTGCTGATTGG | 1840 |
rs73427718 | snp | A/G | 0.00874735 | 0.0655527 | upstream-variant-2KB | DTX1 | GRCh38.p7 | 12:113056207 | CAGGAGATTCAGATC[A/G]GGGTTGGTGTCTGGG | 1840 |
rs73427732 | snp | C/T | 0.0633504 | 0.166319 | intron-variant | DTX1 | GRCh38.p7 | 12:113063044 | AGAGTCAGAGCTGGG[C/T]GAGGGATGGGTCGCT | 1840 |
rs73427738 | snp | G/T | 0.225597 | 0.248806 | intron-variant | DTX1 | GRCh38.p7 | 12:113065393 | GCCCTTCCCAGGCTC[G/T]CCCGGGCCACCGAGT | 1840 |
rs73427748 | snp | G/T | 0.0554779 | 0.157039 | intron-variant | DTX1 | GRCh38.p7 | 12:113074474 | AGCAAGGAGGCCAGG[G/T]TGGCTGGAATGGAGT | 1840 |
rs73427751 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | DTX1 | GRCh38.p7 | 12:113077094 | CCCACCCTGTTTGGT[A/G]GCTCTCCCGCCCCTA | 1840 |
rs73427758 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | DTX1 | GRCh38.p7 | 12:113079914 | TCCCTCTCCTTCCTT[C/G]AGCCTCAGTTTTGTC | 1840 |
rs73427760 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | DTX1 | GRCh38.p7 | 12:113080234 | GAGGGGGTCAAAGAA[A/G]ACCCCTTGGGGAAGC | 1840 |
rs74317265 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | DTX1 | GRCh38.p7 | 12:113071795 | GGGCAGGCGGGCAGC[A/G]GCGGGCGCTGCGGGG | 1840 |
rs74476453 | snp | A/C | 0.5 | 0 | intron-variant | DTX1 | GRCh38.p7 | 12:113066529 | TGAGACTCCGTCTCA[A/C]AAAAAAAAAAAAGAA | 1840 |
rs74906421 | snp | C/T | 0.0554779 | 0.157039 | intron-variant | DTX1 | GRCh38.p7 | 12:113070179 | CTAAACACACTCTTT[C/T]GCTTGAATGAGCTAA | 1840 |
rs74941279 | snp | A/G | 0 | 0 | intron-variant | DTX1 | GRCh38.p7 | 12:113066541 | TCAAAAAAAAAAAAA[A/G]GAATCGTAGTGGGTG | 1840 |
rs75145802 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | DTX1 | GRCh38.p7 | 12:113063178 | CATATGGGAAGCCCA[A/G]GGCCGAAGGGTATGC | 1840 |
rs75237485 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | DTX1 | GRCh38.p7 | 12:113095677 | TTGACTGTGGTCACA[A/G]AGAAACTAAGTGGCG | 1840 |
rs75296180 | snp | C/T | 0.0551013 | 0.156571 | intron-variant | DTX1 | GRCh38.p7 | 12:113066921 | GTCTCCTCTAGGTCC[C/T]GCATAGTTGTGTCCT | 1840 |
rs75402715 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113078545 | TAGGAGAGCTATGGT[A/G]CCTTCTCATTTATTC | 1840 |
rs75811764 | snp | C/T | 0.177503 | 0.239258 | intron-variant | DTX1 | GRCh38.p7 | 12:113077108 | TGGCTCTCCCGCCCC[C/T]ACGCCCAATCTACTG | 1840 |
rs76053890 | snp | C/T | 0.0376037 | 0.131863 | intron-variant | DTX1 | GRCh38.p7 | 12:113062663 | GTACACGTGCGTGTG[C/T]GTACACACACACAGC | 1840 |
rs76083573 | in-del | -/AA | | | intron-variant | DTX1 | GRCh38.p7 | 12:113066540 | CTCAAAAAAAAAAAA[-/AA]GAATCGTAGTGGGTG | 1840 |
rs76129420 | snp | A/T | 0.159292 | 0.232964 | intron-variant | DTX1 | GRCh38.p7 | 12:113078311 | CTATCTCCATGCATA[A/T]GGACCCTATGAGGTA | 1840 |
rs76189099 | snp | A/G | 0.5 | 0 | intron-variant | DTX1 | GRCh38.p7 | 12:113086275 | AGAAAAAAAAAAAAA[A/G]GCAAAAGAACTGGGG | 1840 |
rs76322701 | snp | A/G | 0.5 | 0 | intron-variant | DTX1 | GRCh38.p7 | 12:113086261 | AAAACCCTGTATCAA[A/G]AAAAAAAAAAAAAAG | 1840 |
rs76356885 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113078686 | GCCCAATTCCAAAGT[C/T]TGTGCTGTGTTGTCT | 1840 |
rs76554565 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113092741 | AACTTACTTGATTCC[C/T]GAATCCTTCTTTCCT | 1840 |
rs76690357 | snp | A/C | 0.00159617 | 0.0282053 | utr-variant-3-prime, nc-transcript-variant | DTX1, RASAL1 | GRCh38.p7 | 12:113097355 | TACAGCCTTGTCTGC[A/C]AACTGGAGGATGCGG | 1840 |
rs76733744 | snp | A/C | 0.0115144 | 0.0749975 | intron-variant | DTX1 | GRCh38.p7 | 12:113069841 | AACAAGGACAACAGC[A/C]GCACCCAACACCTTA | 1840 |
rs76801457 | snp | A/G | 0.5 | 0 | intron-variant | DTX1 | GRCh38.p7 | 12:113093330 | GGTGAGCGTGGCCCG[A/G]AGGAAACGCCCCCTT | 1840 |
rs76801522 | snp | A/T | 0.02016 | 0.0983543 | intron-variant | DTX1 | GRCh38.p7 | 12:113087162 | CCATACCTCTAGATA[A/T]ATCTGAGCCTCCAAT | 1840 |
rs77089919 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113085504 | TCCTGTTTACTGGCC[A/G]TGAGTGGTTCCTTCT | 1840 |
rs77322010 | snp | C/T | 0.0349115 | 0.127424 | intron-variant | DTX1 | GRCh38.p7 | 12:113080039 | GGACTACTTTTGCTC[C/T]CCAGGAGGAGGGTTG | 1840 |
rs77377337 | snp | C/T | 0.0325976 | 0.123435 | intron-variant | DTX1 | GRCh38.p7 | 12:113074458 | GGTGTATTTGAGGAA[C/T]AGCAAGGAGGCCAGG | 1840 |
rs77548479 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | DTX1 | GRCh38.p7 | 12:113061579 | TCCAGCAGGGTTGTC[A/G]GGTTGAACAGAGAGA | 1840 |
rs77550984 | snp | A/G | 0.0244538 | 0.107838 | intron-variant | DTX1 | GRCh38.p7 | 12:113093091 | GAGCCAGAGACAGAA[A/G]GCAAGCCAGGTCCCC | 1840 |
rs77668235 | snp | A/C | 0.5 | 0 | intron-variant, downstream-variant-500B | DTX1, RASAL1 | GRCh38.p7 | 12:113096216 | TCACAAAAAAAAAAA[A/C]AGGCAGGCCAAGCGC | 1840 |
rs77720207 | snp | A/C | 0.00993419 | 0.0697739 | intron-variant | DTX1 | GRCh38.p7 | 12:113075132 | CAACTGTTGCTACAG[A/C]TGGCAAACGCAGCAG | 1840 |
rs77763772 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | DTX1 | GRCh38.p7 | 12:113081745 | GGGCTGGAGTGAGGC[A/G]CCAGCAAGAAGGAGA | 1840 |
rs77796846 | snp | C/T | 0.116138 | 0.211142 | intron-variant | DTX1 | GRCh38.p7 | 12:113070861 | AAGAGTTCACCTCTC[C/T]GGGCCTCAGTTTCCT | 1840 |
rs77854998 | snp | A/G | 0.5 | 0 | intron-variant | DTX1 | GRCh38.p7 | 12:113066383 | AAAATACAAAAATTA[A/G]TGGGCATGGTGGTGG | 1840 |
rs77866233 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | DTX1 | GRCh38.p7 | 12:113059596 | TCTGTGACAAGCTCC[A/G]TGGGCAGTGGGGACT | 1840 |
rs78092684 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | DTX1, RASAL1 | GRCh38.p7 | 12:113097545 | AGCAGTTCTACAAAA[A/G]AATGGCCAGCACGAG | 1840 |
rs78776623 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | DTX1 | GRCh38.p7 | 12:113094165 | GGAACCCTCACCCCT[C/T]CTCCTGGGTTCTGGG | 1840 |
rs79438468 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | DTX1 | GRCh38.p7 | 12:113070259 | GTATTATGACTTCTG[A/G]GTTGGTGAAGGATTC | 1840 |
rs79540009 | snp | A/G | 0.0170251 | 0.090679 | utr-variant-3-prime, nc-transcript-variant | DTX1, RASAL1 | GRCh38.p7 | 12:113097215 | CACACACAAACACAC[A/G]TGTCCTGTTGAACTC | 1840 |
rs79742818 | snp | G/T | 0.5 | 0 | intron-variant | DTX1 | GRCh38.p7 | 12:113085702 | TTTTTAATTAATTCA[G/T]TCATATTTATTGAAT | 1840 |
rs79885913 | snp | A/G | 0.5 | 0 | intron-variant | DTX1 | GRCh38.p7 | 12:113086276 | GAAAAAAAAAAAAAA[A/G]CAAAAGAACTGGGGG | 1840 |
rs79910852 | snp | A/G | 0.106633 | 0.204807 | intron-variant | DTX1 | GRCh38.p7 | 12:113080691 | TAAGAATTGTTACAT[A/G]TAGCCTGGGAACAGT | 1840 |
rs80010427 | snp | A/G | 0.170408 | 0.236992 | intron-variant | DTX1 | GRCh38.p7 | 12:113082095 | CGCTCCCCCACAGCC[A/G]ACATCATTTCTCCTG | 1840 |
rs80041861 | snp | C/T | 0.0170251 | 0.090679 | intron-variant, utr-variant-3-prime, nc-transcript-variant | DTX1, RASAL1 | GRCh38.p7 | 12:113096580 | AAATGGCCAAGCCAG[C/T]AGTACGTAGTTGGTG | 1840 |
rs80079963 | snp | C/T | 0.5 | 0 | intron-variant | DTX1 | GRCh38.p7 | 12:113088289 | TCCTGGAGCACTGTG[C/T]TGAGGAGGATTCTGA | 1840 |
rs80204171 | snp | A/G | 0.0287284 | 0.116357 | utr-variant-3-prime, nc-transcript-variant | DTX1, RASAL1 | GRCh38.p7 | 12:113097950 | GTCAGCCAAGATTTA[A/G]AGGGATGCCAGCGAT | 1840 |
rs111233046 | snp | A/G | 0.00903315 | 0.0665956 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant | DTX1, RASAL1 | GRCh38.p7 | 12:113096864 | GGGCCACGGCTACCC[A/G]GACGCTAGCTACCTA | 1840 |
rs111327121 | in-del | -/GAATG/GAATGGAATG/GAATGGAATGGAATG | 0.499172 | 0.268133 | intron-variant | DTX1 | GRCh38.p7 | 12:113080589 | AATTTTCTTGGAACA[lengthTooLong]GAATGGAATGGAATG | 1840 |
rs111360353 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | DTX1 | GRCh38.p7 | 12:113063045 | GAGTCAGAGCTGGGC[A/G]AGGGATGGGTCGCTT | 1840 |
rs111411011 | snp | G/T | 0.0850919 | 0.187897 | intron-variant | DTX1 | GRCh38.p7 | 12:113089146 | GGAAAGGGTCAGCAA[G/T]TGCAAAGGCCCTGGG | 1840 |
rs111503931 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | DTX1 | GRCh38.p7 | 12:113064443 | CTGGGCTGGGTCTTG[A/G]GGACTCAGAGAGAAG | 1840 |
rs111574936 | snp | C/T | 0.5 | 0 | intron-variant | DTX1 | GRCh38.p7 | 12:113086885 | GTCACCCCGCCTCAC[C/T]GCTGCTGCAAGGTCA | 1840 |
rs111605636 | snp | G/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113077389 | CGCAGACCAACGCCC[G/T]CTGTGCTGACGCCTC | 1840 |
rs111637231 | snp | C/T | | | intron-variant, downstream-variant-500B | DTX1, RASAL1 | GRCh38.p7 | 12:113096245 | GCAGTGGTGCACACC[C/T]GTAATCCCTGCACTT | 1840 |
rs111647982 | in-del | -/TT | 0.0535932 | 0.154675 | intron-variant | DTX1 | GRCh38.p7 | 12:113092527 | CCTAGGGGCTCTTCA[-/TT]TGAAGAGAGGATAGT | 1840 |
rs111666052 | snp | C/G | 0.0279526 | 0.114869 | intron-variant | DTX1 | GRCh38.p7 | 12:113080495 | AGAACCTTCTCTCTG[C/G]GTAAATTTATTGTAA | 1840 |
rs111669012 | snp | A/G | 0.5 | 0 | intron-variant | DTX1 | GRCh38.p7 | 12:113068016 | TGCAATCCACCCTGG[A/G]CAACAGAGTGAGATC | 1840 |
rs111958656 | snp | A/T | 0.147991 | 0.228242 | intron-variant | DTX1 | GRCh38.p7 | 12:113082790 | TTTTGTAGGGACAGG[A/T]TCTCACTATGTTGCC | 1840 |
rs111989768 | snp | A/T | 0.0138799 | 0.0821421 | intron-variant | DTX1 | GRCh38.p7 | 12:113078235 | AAGTAATATCCAGCA[A/T]GCACTAAATGTTCAT | 1840 |
rs112159279 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113079306 | CACTATGGCATGGCC[A/G]GGGGAATTGATAATG | 1840 |
rs112245835 | snp | C/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113093499 | GGGGGTTTGGGCGGG[C/G]ATGGCGCCCCGCCCT | 1840 |
rs112268147 | snp | C/T | 0.150333 | 0.229274 | intron-variant | DTX1 | GRCh38.p7 | 12:113074166 | CCTGGGAGGCAGAGG[C/T]TGCAGTGAGCCGAGA | 1840 |
rs112349490 | snp | C/T | 0.0283406 | 0.115616 | intron-variant | DTX1 | GRCh38.p7 | 12:113082538 | GTCTACCCACTGTCA[C/T]TCTCGTCCCCAAACC | 1840 |
rs112426107 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | DTX1 | GRCh38.p7 | 12:113071806 | CAGCGGCGGGCGCTG[C/T]GGGGTGCAGGGCCCA | 1840 |
rs112464619 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | DTX1 | GRCh38.p7 | 12:113075885 | AATATCGCTCGAGCA[C/T]CTGCTGTGTGCAGGT | 1840 |
rs112464998 | snp | A/G | 0.5 | 0 | intron-variant | DTX1 | GRCh38.p7 | 12:113089328 | GCTGCAGGAGGAGTG[A/G]GAGCAGAGGACAGAT | 1840 |
rs112526578 | snp | C/T | 0 | 0 | intron-variant | DTX1 | GRCh38.p7 | 12:113090782 | AAGTGGGTGTGTGTG[C/T]GCTGCACCTGTGTGC | 1840 |
rs112638501 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | DTX1 | GRCh38.p7 | 12:113055938 | GCTGGAGGACAGGGG[C/G]ACTGGCCATCCCGTT | 1840 |
rs112807040 | snp | C/T | 0.00194735 | 0.031143 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant | DTX1, RASAL1 | GRCh38.p7 | 12:113096786 | GTCCAACACCACGGG[C/T]GAGTCGGACACCGTG | 1840 |
rs113004114 | snp | C/T | 0.00463599 | 0.0479219 | synonymous-codon | DTX1 | GRCh38.p7 | 12:113093165 | TTCTCCCCGCAGGGT[C/T]CCCGCACTCCCGGTG | 1840 |
rs113024514 | snp | G/T | 0.5 | 0 | intron-variant | DTX1 | GRCh38.p7 | 12:113080262 | AGCCTTGTCCAAAGC[G/T]GCAGGATAGAGTCAC | 1840 |
rs113220379 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | DTX1 | GRCh38.p7 | 12:113083352 | TTTTTTTTTGAGACC[A/G]TCTTGCTCTGTTACC | 1840 |
rs113226560 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DTX1 | GRCh38.p7 | 12:113086381 | GAGAAGGCCAGTGTG[A/G]TTGGAGAGGCTCAGG | 1840 |
rs113289700 | in-del | -/T | 0.147656 | 0.228091 | intron-variant | DTX1 | GRCh38.p7 | 12:113061872 | ACCACACCCGGCTAA[-/T]TTTTTGTATTTTTAG | 1840 |
rs113332852 | snp | C/G | 0.444444 | 0.157135 | intron-variant | DTX1 | GRCh38.p7 | 12:113075965 | TACATTCTAGCGAGG[C/G]GGGGACAGACAGAAA | 1840 |
rs113426042 | snp | A/G | 0.00517822 | 0.0506191 | utr-variant-5-prime | DTX1 | GRCh38.p7 | 12:113057872 | CGAACAGGGGCGGCT[A/G]CCTCACTCCCTACCT | 1840 |
rs113450180 | snp | A/G | 0.5 | 0 | intron-variant | DTX1 | GRCh38.p7 | 12:113095770 | GACTTTCTGCTTTTC[A/G]AGAGCACCAAGAAAT | 1840 |
rs113452746 | snp | C/T | 0.5 | 0 | intron-variant | DTX1 | GRCh38.p7 | 12:113085938 | GCCTCATGGAGAAGG[C/T]AATACCTTCTTGAGC | 1840 |
rs113458817 | snp | A/G | 0.0023933 | 0.0345097 | utr-variant-3-prime, nc-transcript-variant | DTX1, RASAL1 | GRCh38.p7 | 12:113097374 | TGGAGGATGCGGGGC[A/G]AGCCCTTAGGGGCCT | 1840 |
rs113562815 | snp | A/G | 0.157972 | 0.232445 | intron-variant | DTX1 | GRCh38.p7 | 12:113069820 | CTGGCACTGCGGAGC[A/G]TTCGGTAAGGTGTTG | 1840 |
rs113596464 | snp | C/T | 0 | 0 | intron-variant | DTX1 | GRCh38.p7 | 12:113090920 | TGTGCAGTGAGTCAG[C/T]GTGTCCTCCTGCGCC | 1840 |
rs113758114 | in-del | -/A | 0.5 | 0 | intron-variant | DTX1 | GRCh38.p7 | 12:113066527 | GTGAGACTCCGTCTC[-/A]AAAAAAAAAAAAAAG | 1840 |
rs113809221 | snp | A/T | 0.5 | 0 | intron-variant | DTX1 | GRCh38.p7 | 12:113058515 | CCTTGCAGCGTAGGA[A/T]GCTGAAAATCCCAGT | 1840 |
rs113983424 | snp | A/C/G/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113081370 | TTGAAAGCTACTGTT[A/C/G/T]TAGAGGAGGCTGAAA | 1840 |
rs114058798 | snp | C/T | 0.0894459 | 0.191631 | intron-variant | DTX1 | GRCh38.p7 | 12:113063700 | CAGGTGGTGGCTGGT[C/T]CTGGGATCTTCCAGC | 1840 |
rs114090558 | snp | C/G | 0.0894459 | 0.191631 | intron-variant | DTX1 | GRCh38.p7 | 12:113069101 | ACGAAGCATTTAGAA[C/G]AGCGCCTGGCACATA | 1840 |
rs114093182 | snp | C/T | 0.0509478 | 0.151255 | intron-variant | DTX1 | GRCh38.p7 | 12:113090411 | TTCCTGGGGCCCCCC[C/T]GCAGGGTGCCCGACA | 1840 |
rs114232024 | snp | C/T | 0.00447184 | 0.0470736 | intron-variant, utr-variant-3-prime, nc-transcript-variant | DTX1, RASAL1 | GRCh38.p7 | 12:113096687 | CCTGTGACCTCCTCC[C/T]GGCCCCACTGTGTCC | 1840 |
rs114237068 | snp | G/T | 0.0126979 | 0.078662 | intron-variant | DTX1 | GRCh38.p7 | 12:113075444 | TTCCCGCAGTTGAGG[G/T]GAAGTCAAGTGTGCA | 1840 |
rs114271670 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | DTX1 | GRCh38.p7 | 12:113070818 | CACGAGTGTGGCATC[A/G]TTCCCAGCCCTCTGC | 1840 |
rs114465748 | snp | A/C | 0.0633504 | 0.166319 | intron-variant | DTX1 | GRCh38.p7 | 12:113090135 | AGGTAGTCCTGGAGA[A/C]AAAAAGAGATACTTT | 1840 |
rs114489492 | snp | C/T | 0.0391387 | 0.134304 | intron-variant | DTX1 | GRCh38.p7 | 12:113071991 | GCTAGCTGGCCCTGA[C/T]GGGCTCCCAGAGTCC | 1840 |
rs114513792 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | DTX1 | GRCh38.p7 | 12:113066568 | GGTGGGGAGATTTGT[G/T]ACCTTAAGTAAACCA | 1840 |
rs114552367 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | DTX1 | GRCh38.p7 | 12:113070485 | TGGGCCTTGAAGCTG[A/G]CCCAGCCCAGAGAGG | 1840 |
rs114590160 | snp | A/G | 0.100231 | 0.200173 | upstream-variant-2KB | DTX1 | GRCh38.p7 | 12:113055047 | CTCACTCTAGCAGGG[A/G]CAGATTTCATTTAAG | 1840 |
rs114830827 | snp | C/T | 0.0569829 | 0.158885 | intron-variant | DTX1 | GRCh38.p7 | 12:113067537 | GAAGTGTGTGCAGTG[C/T]CTGGGAAGGCAGAGG | 1840 |
rs114844328 | snp | C/T | 0.0452528 | 0.143452 | upstream-variant-2KB | DTX1 | GRCh38.p7 | 12:113055831 | GCTGGAGTTCCCGGA[C/T]GCATCCTTCATCTTC | 1840 |
rs114871961 | snp | C/T | 0.0093238 | 0.0676385 | intron-variant | DTX1 | GRCh38.p7 | 12:113095281 | TTCTCCACCCTGCCA[C/T]CACCTGTTCATGGTC | 1840 |
rs114887362 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | DTX1 | GRCh38.p7 | 12:113061449 | TGTCCTCATTGGTAA[C/T]GCACTGGAAAAGAGC | 1840 |
rs114937205 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | DTX1 | GRCh38.p7 | 12:113091940 | CATCAACAGCAAGAC[A/T]CCAGTTCCCCTGCAT | 1840 |
rs115046593 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | DTX1 | GRCh38.p7 | 12:113074978 | CAGAGCTGAGTTCAA[A/G]GTGCCTGTTAAACCT | 1840 |
rs115143586 | snp | C/G | 0.11963 | 0.213316 | intron-variant | DTX1 | GRCh38.p7 | 12:113064874 | CATGGTGTATGCCTG[C/G]AGCCTCTGAGAGGAG | 1840 |
rs115160030 | snp | G/T | 0.0391387 | 0.134304 | intron-variant | DTX1 | GRCh38.p7 | 12:113071632 | TGGCTGAAAATCTAG[G/T]CCATGGCCACTGCGG | 1840 |
rs115228516 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | DTX1 | GRCh38.p7 | 12:113070762 | CCACTTGGTGAGGTT[A/G]AACCCCATGGAACCA | 1840 |
rs115315057 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | DTX1 | GRCh38.p7 | 12:113071798 | CAGGCGGGCAGCGGC[A/G]GGCGCTGCGGGGTGC | 1840 |
rs115355679 | snp | A/G | 0.0905309 | 0.192535 | intron-variant | DTX1 | GRCh38.p7 | 12:113064849 | ACGGTGCCTTCAGCC[A/G]TGGGATGTGCATGGT | 1840 |
rs115392890 | snp | A/G | 0.0448719 | 0.142907 | intron-variant | DTX1 | GRCh38.p7 | 12:113074899 | AGAGCATCCGGAAGC[A/G]CAGGAGCTGCCAGGA | 1840 |
rs115473393 | snp | C/G | 0.108048 | 0.20579 | intron-variant | DTX1 | GRCh38.p7 | 12:113066554 | AAAGAATCGTAGTGG[C/G]TGGGGAGATTTGTGA | 1840 |
rs115473530 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | DTX1 | GRCh38.p7 | 12:113087711 | GGCTCCTGGGGCTCT[C/T]TGGGGTCTGCTGGGT | 1840 |
rs115514062 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | DTX1 | GRCh38.p7 | 12:113087068 | TCCCTGCCCCCAACC[A/G]TCTCCTCCCGTTCCT | 1840 |
rs115794841 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | DTX1 | GRCh38.p7 | 12:113073770 | GGCACCCGAGGAAGA[G/T]GCCAATTAACAATGG | 1840 |
rs115945382 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | DTX1 | GRCh38.p7 | 12:113059958 | GCATTGTTGCAGAAA[A/G]TTCTATTACACCATG | 1840 |
rs116015164 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | DTX1 | GRCh38.p7 | 12:113071442 | CCGAGGCAGAGGCAC[A/G]GAGCCCATGTTTGTC | 1840 |
rs116126616 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DTX1 | GRCh38.p7 | 12:113070978 | GCAGCATGTGCCATA[C/T]AGTAGGTGCTCAATA | 1840 |
rs116146396 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | DTX1 | GRCh38.p7 | 12:113070078 | TGGACCACTCACAGA[C/T]GGCATCCGGTGTGCT | 1840 |
rs116227698 | snp | C/G | 0.00703268 | 0.0588803 | intron-variant | DTX1 | GRCh38.p7 | 12:113077380 | TTCCAGCCGCGCAGA[C/G]CAACGCCCGCTGTGC | 1840 |
rs116268843 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | DTX1 | GRCh38.p7 | 12:113060560 | AGGACATTTAAGTCC[A/G]TTCTGTTTGGGATGC | 1840 |
rs116360778 | snp | C/G | 0.0998734 | 0.199905 | upstream-variant-2KB, utr-variant-5-prime | DTX1 | GRCh38.p7 | 12:113057663 | TCGGCAGGAGCCGTC[C/G]GAGAAGGGGGCCCAG | 1840 |
rs116607652 | snp | G/T | 0.0596104 | 0.162024 | intron-variant | DTX1 | GRCh38.p7 | 12:113080818 | CCATCTCTACAACAA[G/T]AACAAAAAATTAGCC | 1840 |
rs116685496 | snp | C/G/T | 0.00955014 | 0.068563 | intron-variant | DTX1 | GRCh38.p7 | 12:113070238 | TCTGAGTGTGGATGG[C/G/T]TGTTAGTATTATGAC | 1840 |
rs116763556 | snp | A/C | 0.000399281 | 0.0141238 | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | RASAL1, DTX1 | GRCh38.p7 | 12:113098473 | CAACATGCCAGGACG[A/C]CCCTGTAGTTCTGGT | 1840 |
rs116800762 | snp | G/T | 0.0197459 | 0.097381 | synonymous-codon | DTX1 | GRCh38.p7 | 12:113077467 | CTACGACCCGTCGTC[G/T]GCGCCGGGCAAGGGC | 1840 |
rs117006174 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | DTX1 | GRCh38.p7 | 12:113091902 | CCTCTTCATCAGAAC[A/G]TATCCAGCCTGGGTT | 1840 |
rs117007238 | snp | A/G | 0.00755907 | 0.0610114 | upstream-variant-2KB | DTX1 | GRCh38.p7 | 12:113055065 | GATTTCATTTAAGAG[A/G]CTAATTGTGATACAG | 1840 |
rs117158926 | snp | A/G | 0.0244538 | 0.107838 | intron-variant | DTX1 | GRCh38.p7 | 12:113074402 | CATATTCCAGGCAGA[A/G]GGAACAGCCAGTGAG | 1840 |
rs117173461 | snp | A/G | 0.0498117 | 0.149749 | intron-variant | DTX1 | GRCh38.p7 | 12:113081086 | ATATTTGAGGCGGGC[A/G]TAGTGGCTCACTTTG | 1840 |
rs117201988 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | DTX1 | GRCh38.p7 | 12:113069182 | ATTATGCCATTTCAC[A/G]GATGAGAAAGGAGCA | 1840 |
rs117220230 | snp | C/G | 0.0119091 | 0.0762411 | intron-variant | DTX1 | GRCh38.p7 | 12:113087019 | GCCGTGGGAACAGCC[C/G]GTCCTGCCCTCCCCT | 1840 |
rs117253571 | snp | A/C | 0.0165278 | 0.0893908 | intron-variant | DTX1 | GRCh38.p7 | 12:113084021 | TTCAATGTCATTCTC[A/C]CCTCCAACCTCATCT | 1840 |
rs117278604 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113061528 | CTCTCCAGGTCTCAG[C/T]TTCCACATCCGTGAA | 1840 |
rs117402567 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113069548 | CCACAGCTTAGCCTG[A/C]TGAATCCCAGAGGAG | 1840 |
rs117558786 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | DTX1 | GRCh38.p7 | 12:113073880 | ACAAGATCCCTGACT[C/T]TGCAGCTGACAGCCT | 1840 |
rs117591489 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | DTX1 | GRCh38.p7 | 12:113087272 | AGACAGAAGTAAGGG[G/T]TCCCATTTCACAGAG | 1840 |
rs117606358 | snp | A/T | 0.0146672 | 0.084371 | intron-variant | DTX1 | GRCh38.p7 | 12:113089566 | AGGATGTTCTCACTG[A/T]CTCGGAGGAAACAGC | 1840 |
rs117611588 | snp | A/G | 0.021333 | 0.101051 | intron-variant | DTX1 | GRCh38.p7 | 12:113087847 | AGGAGACCAGACTTT[A/G]GAGGAGGGAGGGGAC | 1840 |
rs117665842 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | DTX1 | GRCh38.p7 | 12:113077317 | CCCCTGGAGGCCTGT[A/G]CTGACCCCCCAACCT | 1840 |
rs117737558 | snp | C/G | 0.0726307 | 0.176182 | upstream-variant-2KB, intron-variant | DTX1 | GRCh38.p7 | 12:113057196 | CGGCAGGGCGAGGGC[C/G]CCGGGGGAAGGGAAG | 1840 |
rs117741238 | snp | C/G | 0.0349115 | 0.127424 | upstream-variant-2KB | DTX1 | GRCh38.p7 | 12:113055887 | AGGTGGTCCACCCCC[C/G]TCCCAGCCAATGTGT | 1840 |
rs118091373 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | DTX1 | GRCh38.p7 | 12:113079060 | GTTTGCAAATTCTTG[A/G]GTTAAGGTGTCCCAG | 1840 |
rs137908297 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DTX1 | GRCh38.p7 | 12:113060272 | CTAAGCACTGGAGTA[C/T]AGCAGGGAGCAAGAC | 1840 |
rs137999152 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113073653 | AGCCCTTGTGATTCT[A/C]ACAGAGGAGAGGGCA | 1840 |
rs138057258 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | DTX1 | GRCh38.p7 | 12:113069280 | GCTAGGGATCTGAAT[C/T]CCCTGCTGGGTGTGT | 1840 |
rs138126342 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | DTX1 | GRCh38.p7 | 12:113085646 | CCCATCTTTTCTGTA[A/G]TTTGCTGTTTCTTTT | 1840 |
rs138150287 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant, utr-variant-3-prime, nc-transcript-variant | DTX1, RASAL1 | GRCh38.p7 | 12:113096551 | TGGAAGTTCAGGAAA[C/T]ACAAATGCAAAGGAA | 1840 |
rs138351442 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113084353 | CTATTTCCATTTATC[A/G]AGCGCTCCCTATGTC | 1840 |
rs138437782 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | DTX1 | GRCh38.p7 | 12:113090460 | CACTCTCATCCCTGC[A/G]CCAAATGATGAGCTT | 1840 |
rs138441276 | snp | A/G | 3.3716e-05 | 0.00410571 | missense | DTX1 | GRCh38.p7 | 12:113094895 | GCCTGGGCCGCTGTG[A/G]CCACATGTACCACCT | 1840 |
rs138593139 | snp | C/G/T | 0.00398564 | 0.0444627 | intron-variant | DTX1 | GRCh38.p7 | 12:113095923 | CCAGAAAAAAACAGG[C/G/T]AGGGCCGGGTGTGGT | 1840 |
rs138749950 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113060105 | TCTGGAAACACAGGC[A/G]AATTCATAACAAATG | 1840 |
rs138783164 | snp | C/T | 0.0111196 | 0.0737302 | upstream-variant-2KB | DTX1 | GRCh38.p7 | 12:113054867 | GCTTCAGGAGGTTTT[C/T]TGTTTCCTTGTGTAA | 1840 |
rs138997202 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113078960 | CTGCTCTTGTTTTAA[C/T]CAGAGCAGCCCTTTT | 1840 |
rs139031050 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | DTX1 | GRCh38.p7 | 12:113074893 | CAAGGAAGAGCATCC[A/G]GAAGCGCAGGAGCTG | 1840 |
rs139039787 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113090208 | CTAGACTTAACCAGG[C/T]TGTCTGCACTAGAGG | 1840 |
rs139083094 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DTX1 | GRCh38.p7 | 12:113091418 | GTAGACGGATGGGGA[A/G]GGAGGCTCCCTGGTA | 1840 |
rs139147166 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DTX1 | GRCh38.p7 | 12:113088323 | TGCATCTTGGCTTAG[C/T]GGTAAGGCATGCCGA | 1840 |
rs139210315 | in-del | -/T | 0.02016 | 0.0983543 | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | DTX1, RASAL1 | GRCh38.p7 | 12:113098079 | TCTGTTCCTGGGGGC[-/T]TGCAGTCAGCCCCGT | 1840 |
rs139246816 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113062346 | AAAGCAGCATAGACA[A/G]TATGTAAGTGAATGC | 1840 |
rs139255873 | snp | C/G | 0.0252325 | 0.109451 | intron-variant | DTX1 | GRCh38.p7 | 12:113064328 | TTCTACTATTGCAGA[C/G]CCATGGTCTCTGGCT | 1840 |
rs139291370 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | DTX1 | GRCh38.p7 | 12:113075035 | TCCCAGGGGAGAAGA[C/T]GGGGCCAAAGATGGC | 1840 |
rs139354380 | snp | A/G | 1.8274e-05 | 0.00302269 | intron-variant | DTX1 | GRCh38.p7 | 12:113058490 | CACCCGCCCCGCCGA[A/G]CCATCACTACCTTGC | 1840 |
rs139419148 | snp | C/T | 8.30117e-05 | 0.00644197 | synonymous-codon | DTX1 | GRCh38.p7 | 12:113058363 | GAAGGAGGACGCTCG[C/T]GGTTCCGTGGTCCTG | 1840 |
rs139425541 | in-del | -/A | 0.0486741 | 0.148216 | intron-variant | DTX1 | GRCh38.p7 | 12:113077328 | CTGTGCTGACCCCCC[-/A]ACCTCCCGCCCACCC | 1840 |
rs139547488 | in-del | -/TTTC | 0.100588 | 0.200439 | upstream-variant-2KB, utr-variant-5-prime | DTX1 | GRCh38.p7 | 12:113056805 | GTCCACGCGCGGAAA[-/TTTC]GCTCGGCGCGGCGGC | 1840 |
rs139652234 | snp | A/G/T | 0.0103295 | 0.0711199 | intron-variant | DTX1 | GRCh38.p7 | 12:113086727 | ATTTTCTTTCTCCAG[A/G/T]TCTTCCATAAGTATT | 1840 |
rs139738461 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | DTX1 | GRCh38.p7 | 12:113081782 | CCCCAGGCAGGGCAT[C/T]GCAGGTGCAAAGGGG | 1840 |
rs139788602 | in-del | -/T | 0.474813 | 0.109357 | intron-variant | DTX1 | GRCh38.p7 | 12:113085054 | CTCAGGCCCGTACCC[-/T]TTTTTTTTTTTTTTA | 1840 |
rs139805637 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DTX1 | GRCh38.p7 | 12:113076118 | CTGAATGCCTGAATA[C/T]GGGAGTGGGCTGAAG | 1840 |
rs139808771 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DTX1 | GRCh38.p7 | 12:113081202 | ACAAAAATTAGCTGA[A/G]CATGGTGGTACACAC | 1840 |
rs139852284 | snp | C/T | 0.00438332 | 0.0466095 | utr-variant-3-prime, nc-transcript-variant | DTX1, RASAL1 | GRCh38.p7 | 12:113097240 | GAACTCATGCACGCA[C/T]ACCCACGTGCCTGTA | 1840 |
rs140029285 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113070316 | CACTGCCCAACCCCC[A/C/G]GTCACAGGCCTCAGC | 1840 |
rs140061240 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | DTX1 | GRCh38.p7 | 12:113065250 | TCTGGGTTCCCTTCA[C/T]CCAGCCAGCGGGTGT | 1840 |
rs140099273 | in-del | -/TG | 0.105924 | 0.204309 | intron-variant | DTX1 | GRCh38.p7 | 12:113091246 | GTGTGCACAAGTCTC[-/TG]TATGTAGGTGTGGGG | 1840 |
rs140229626 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | DTX1, RASAL1 | GRCh38.p7 | 12:113097561 | AATGGCCAGCACGAG[C/T]GGGGACTAGAGGGTC | 1840 |
rs140296891 | snp | C/G | 0.0248432 | 0.108648 | intron-variant | DTX1 | GRCh38.p7 | 12:113083459 | GCCTCCCAAGTAGTG[C/G]AGATTACAGACACCT | 1840 |
rs140339922 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DTX1 | GRCh38.p7 | 12:113066167 | GGAACCTGGAAACAG[C/T]TACCTCGGGGAATGC | 1840 |
rs140369488 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113062561 | GACCCCTGCCCCACA[A/T]GTTCTGAACCTGAGC | 1840 |
rs140431071 | snp | A/C | 0.0111196 | 0.0737302 | intron-variant | DTX1 | GRCh38.p7 | 12:113060955 | GACAGACTCCCCACA[A/C]GGCTGCCAAGTTGGC | 1840 |
rs140530968 | in-del | -/GGGTGTGTAGGCC | 0.0543475 | 0.155628 | intron-variant | DTX1 | GRCh38.p7 | 12:113066238 | TTACTAAGAATCATG[-/GGGTGTGTAGGCC]GGGTGTGGTGGCTCA | 1840 |
rs140661134 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | DTX1 | GRCh38.p7 | 12:113088593 | TGCACATGTACCCTA[G/T]AACTTAAAGTATAAT | 1840 |
rs140694825 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DTX1 | GRCh38.p7 | 12:113084200 | CTGGGCCTGGGGGAC[C/T]TGCGGGGGTGGGGAA | 1840 |
rs140752081 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113076775 | AATGACTAAATGAAA[G/T]AGTGCTTAAATTAAT | 1840 |
rs140829150 | in-del | -/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113076999 | CCCCACTTCAGTGTC[-/T]TGTCTTGGCCCTGGA | 1840 |
rs140856956 | snp | A/C/T | 0.00835141 | 0.0640778 | intron-variant | DTX1 | GRCh38.p7 | 12:113071694 | TAGAAATCTTGAGAT[A/C/T]GAAGTCCAGGCAGGT | 1840 |
rs140926138 | snp | A/C/T | 9.07472e-05 | 0.00673546 | synonymous-codon | DTX1 | GRCh38.p7 | 12:113093621 | CCTGCACCCGCCGCC[A/C/T]GTGAGCAAGAGCGAC | 1840 |
rs140996619 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | DTX1 | GRCh38.p7 | 12:113061620 | TTTTATCCCACAAAC[A/G]TCAACTAATTATCTA | 1840 |
rs141002060 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113059879 | TCTCACTAGCCACAC[G/T]TCAAGTGCTCATAGC | 1840 |
rs141002319 | snp | A/G | 0.00615174 | 0.0551183 | intron-variant | DTX1 | GRCh38.p7 | 12:113095219 | GTGGGCTCCCCTTCC[A/G]CCTCTCTGGCCCCCA | 1840 |
rs141058125 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DTX1 | GRCh38.p7 | 12:113058940 | AGTGATTTAAACTCA[A/G]AGCTGGGATTTAAAC | 1840 |
rs141107954 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | DTX1 | GRCh38.p7 | 12:113089818 | CTATGTGGTATTTAA[A/G]GGGCTCCAGAAATTT | 1840 |
rs141124242 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | DTX1 | GRCh38.p7 | 12:113073467 | AAGTTTTTGTCTGAT[A/T]GGCTGGAACATGGTA | 1840 |
rs141189025 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113068565 | ATAACCGCACACACG[A/G]TATGTTCAAAAAATA | 1840 |
rs141206415 | snp | C/T | 0.0166325 | 0.0896639 | utr-variant-3-prime, nc-transcript-variant | DTX1, RASAL1 | GRCh38.p7 | 12:113097246 | ATGCACGCACACCCA[C/T]GTGCCTGTACTTGCC | 1840 |
rs141286238 | in-del | -/AGG | 0.0532157 | 0.154195 | intron-variant | DTX1 | GRCh38.p7 | 12:113065829 | CCAAGGGGTTGGGGC[-/AGG]ACTGGTCACAGTGGC | 1840 |
rs141314991 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DTX1 | GRCh38.p7 | 12:113062437 | TCACGGGTCATGAAA[C/T]ATTCTTTTTTTTCCC | 1840 |
rs141350877 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113090960 | GATGTGAATCAGTAC[A/G]CACGAGTACTTCCCC | 1840 |
rs141505500 | snp | G/T | 0.00199481 | 0.0315187 | upstream-variant-2KB | DTX1 | GRCh38.p7 | 12:113054982 | AGTAAATGACACCCT[G/T]ATGTAATGGGGCACC | 1840 |
rs141508768 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113069553 | GCTTAGCCTGATGAA[G/T]CCCAGAGGAGAGTTT | 1840 |
rs141608807 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DTX1 | GRCh38.p7 | 12:113090273 | GAGGGAAATGCCTCT[A/G]TGCATTCCTATAAAA | 1840 |
rs141617258 | in-del | -/C | | | intron-variant | DTX1 | GRCh38.p7 | 12:113065138 | CCAGGCCCCGGGGGA[-/C]CTCACAGCCACGCTG | 1840 |
rs141617919 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | DTX1 | GRCh38.p7 | 12:113063182 | TGGGAAGCCCAAGGC[C/T]GAAGGGTATGCTCAG | 1840 |
rs141628130 | snp | A/G | 0.000148993 | 0.00862985 | synonymous-codon | DTX1 | GRCh38.p7 | 12:113095098 | GGAGAAGACGGGTAC[A/G]CAGCCGCCTGGGAAG | 1840 |
rs141693840 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | DTX1 | GRCh38.p7 | 12:113057736 | TCTGGGACGCAGTTG[G/T]GAGTGCAAAGGGCTG | 1840 |
rs141866541 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | DTX1 | GRCh38.p7 | 12:113060212 | TTGTTCATGCATTCC[A/G]TCATATGATTATTTA | 1840 |
rs141939936 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113074900 | GAGCATCCGGAAGCG[C/T]AGGAGCTGCCAGGAA | 1840 |
rs141977619 | snp | C/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113074452 | GTGCCTGGTGTATTT[C/G]AGGAACAGCAAGGAG | 1840 |
rs142086578 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DTX1 | GRCh38.p7 | 12:113082929 | AGTCTGTATTAGTTT[A/G]CTGGGGCAGTGGTAA | 1840 |
rs142162510 | snp | C/T | 6.62493e-05 | 0.00575502 | synonymous-codon | DTX1 | GRCh38.p7 | 12:113077557 | CATCACCATCCAGAA[C/T]GCCTACGAGAAGCAG | 1840 |
rs142267522 | snp | C/T | 0.000502588 | 0.0158443 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant | DTX1, RASAL1 | GRCh38.p7 | 12:113096867 | CCACGGCTACCCGGA[C/T]GCTAGCTACCTAGAC | 1840 |
rs142463652 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | DTX1 | GRCh38.p7 | 12:113093092 | AGCCAGAGACAGAAG[C/G]CAAGCCAGGTCCCCT | 1840 |
rs142597591 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113070844 | TCTGCTCTCACCCTC[C/T]CAAGAGTTCACCTCT | 1840 |
rs142711332 | in-del | -/A | 0.0726307 | 0.176182 | intron-variant | DTX1 | GRCh38.p7 | 12:113086699 | TTATGCTTTTATTTT[-/A]TAAAAAATCCACATT | 1840 |
rs142743893 | in-del | -/G | 0.0551013 | 0.156571 | intron-variant | DTX1 | GRCh38.p7 | 12:113074944 | ACTTCAGGAGGAGCA[-/G]GTTTGGGGCAGGGGA | 1840 |
rs142764472 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113064108 | GACAGCCTGCACTAC[C/G]CTGGAGGCCTCCAGG | 1840 |
rs142778629 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DTX1 | GRCh38.p7 | 12:113064853 | TGCCTTCAGCCATGG[A/G]ATGTGCATGGTGTAT | 1840 |
rs142798548 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113081288 | GAGCCGAGATCACGC[C/T]ACTGCACTCCAGCCT | 1840 |
rs142936190 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | DTX1 | GRCh38.p7 | 12:113089701 | AGACTACCTCGGGAC[A/T]GTCCCCCAGGCTCAC | 1840 |
rs143136677 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113085198 | GGGACTACAGGCGCA[C/T]GCCACCAACCCGGCT | 1840 |
rs143257034 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113084822 | ATTAGGACTCAGATT[C/G]AAAAACCCAAGTTGA | 1840 |
rs143284394 | snp | A/G | 0.0023933 | 0.0345097 | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | RASAL1, DTX1 | GRCh38.p7 | 12:113098504 | GGATGCTGCGGCTTC[A/G]GGCAACCCCTGCTGG | 1840 |
rs143605977 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | DTX1 | GRCh38.p7 | 12:113090756 | CTATCCTGTATAGCC[A/G]AGCAGCCACCAAGTG | 1840 |
rs143671658 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | DTX1 | GRCh38.p7 | 12:113086291 | GCAAAAGAACTGGGG[A/G]AAGAGCATTCCAACA | 1840 |
rs143697544 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | DTX1 | GRCh38.p7 | 12:113065318 | GGTGGGGAGCCGCCT[A/G]CCGACGCTGAGAAGA | 1840 |
rs143713335 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113059492 | TGATGGAGATAAAAT[C/T]GATGAGGTCCCACTC | 1840 |
rs143771350 | in-del | -/GTGTGGATG | | | intron-variant | DTX1 | GRCh38.p7 | 12:113091444 | GGTATCTGTGTGTCT[-/GTGTGGATG]GTGTGTGCATGTATC | 1840 |
rs143820374 | in-del | -/A | | | intron-variant | DTX1 | GRCh38.p7 | 12:113092327 | TCCTCACAGCAGATT[-/A]AAAAAAAAAAAAGGT | 1840 |
rs143941508 | snp | A/G | 1.71664e-05 | 0.00292966 | missense | DTX1 | GRCh38.p7 | 12:113058446 | ACCAGTTTCGCCAGG[A/G]CACAGGTGAGCAGAC | 1840 |
rs143950327 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113060720 | CATTCTTCCAGAGAG[A/G]CACCAAGGACCTGAT | 1840 |
rs143978802 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113061073 | CACTCCCCTTTCATC[A/C]GGCCCCATTCTCTCA | 1840 |
rs143993387 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DTX1 | GRCh38.p7 | 12:113075119 | GCAACCCCACAAGCA[A/G]CTGTTGCTACAGCTG | 1840 |
rs144014904 | snp | A/C/T | 0.000455638 | 0.0150871 | missense, synonymous-codon | DTX1 | GRCh38.p7 | 12:113094944 | GTACTCCAATGGCAA[A/C/T]AAGGTGGGTTGGGCG | 1840 |
rs144113606 | snp | A/C/T | 6.71224e-05 | 0.00579287 | stop-gained, missense, utr-variant-3-prime, nc-transcript-variant | DTX1, RASAL1 | GRCh38.p7 | 12:113096791 | ACACCACGGGCGAGT[A/C/T]GGACACCGTGGTGTG | 1840 |
rs144136028 | snp | C/T | 5.31561e-05 | 0.00515512 | synonymous-codon | DTX1 | GRCh38.p7 | 12:113093168 | TCCCCGCAGGGTCCC[C/T]GCACTCCCGGTGAAG | 1840 |
rs144453228 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | DTX1 | GRCh38.p7 | 12:113087760 | AGGGGGCCAAGGCCA[A/G]TGGGGGACCTGGAAA | 1840 |
rs144457922 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | DTX1 | GRCh38.p7 | 12:113075186 | GCCCATTTTCAACAT[A/G]AGAAAACTGGGGCCC | 1840 |
rs144460174 | snp | C/T | 0.00279162 | 0.0372561 | upstream-variant-2KB | DTX1 | GRCh38.p7 | 12:113056205 | GGCAGGAGATTCAGA[C/T]CGGGGTTGGTGTCTG | 1840 |
rs144525161 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DTX1 | GRCh38.p7 | 12:113072064 | CCTGGCCTGAGGGTC[C/T]TCCCCAGGGACCCCT | 1840 |
rs144740665 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113062454 | TTCTTTTTTTTCCCC[C/T]AACCATTTAAAAATG | 1840 |
rs144805307 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | DTX1 | GRCh38.p7 | 12:113059908 | GCCACATGTGTCTTG[C/T]GGTACCTTGTGGGCC | 1840 |
rs144836577 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | DTX1 | GRCh38.p7 | 12:113064775 | GGATACTACTTTGCA[C/T]GTAGTAAGCACTCAT | 1840 |
rs144872157 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | DTX1 | GRCh38.p7 | 12:113082519 | TGAGGAGCCAGGCAG[A/G]CAGGTCTACCCACTG | 1840 |
rs144931047 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DTX1 | GRCh38.p7 | 12:113061650 | ACTGTGCATCTAGCA[C/T]GTGCTCACCACTGTG | 1840 |
rs144994750 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | DTX1 | GRCh38.p7 | 12:113076269 | TTCGAGACCAGCCTG[A/G]CCAACATGGCAAAAC | 1840 |
rs145076343 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | DTX1 | GRCh38.p7 | 12:113067800 | ACTTTGGGAGGCTGA[C/G]ACAGGAGGATCACTT | 1840 |
rs145093568 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | DTX1 | GRCh38.p7 | 12:113083771 | CTTCTGCCTTTTCCT[C/G]TTAGTCACTCTCTTT | 1840 |
rs145127165 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113078827 | GCTGCACCTGAAATA[C/T]CACAATTACTCTGGG | 1840 |
rs145157755 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113074507 | GTGATAAGGGGGAGG[C/T]AGACAATGCCAGAGG | 1840 |
rs145234735 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113062416 | AATTTGAATTTCATA[C/T]CTTTTTCACGGGTCA | 1840 |
rs145299713 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113082210 | CTCAAGAACTCCCTC[A/G]TCCCTCCCCACCCAC | 1840 |
rs145308615 | in-del | -/C | | | intron-variant | DTX1 | GRCh38.p7 | 12:113091473 | CTGTGATGTACTCCC[-/C]TGGGTTGTGTGTGTT | 1840 |
rs145334642 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | DTX1, RASAL1 | GRCh38.p7 | 12:113097645 | TTCCCATCTCCAGGC[C/T]TTCTGTCTGTCCCAG | 1840 |
rs145365879 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113092185 | ACTTAGTGCCTGGGA[A/C]GCAAAGAGGTGAAAT | 1840 |
rs145534736 | snp | A/G | 0.0379877 | 0.132479 | intron-variant | DTX1 | GRCh38.p7 | 12:113077300 | CCCAAGTCTGGGTGG[A/G]CCCCCTGGAGGCCTG | 1840 |
rs145555819 | snp | A/C | 0.0123036 | 0.0774623 | intron-variant, downstream-variant-500B | DTX1, RASAL1 | GRCh38.p7 | 12:113096283 | CCGAGGTGGGAGGAT[A/C]ACTTGAGGCCAGGAG | 1840 |
rs145607011 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | DTX1 | GRCh38.p7 | 12:113058592 | CAGAAAAACAGGGCA[A/G]TCTAACCTTGTCCAG | 1840 |
rs145613119 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | DTX1 | GRCh38.p7 | 12:113080343 | ATAGACAGCAGCTGG[A/G]CTCTGGCTGCCTTAC | 1840 |
rs145722018 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | DTX1 | GRCh38.p7 | 12:113059356 | TTGGTGGCAGTCTTC[A/G]TGGCCATGTGGTGTG | 1840 |
rs145914363 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113089251 | ACACATAGGAAATGA[A/G]GTTCAGAGGGTAGAT | 1840 |
rs145961828 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | DTX1 | GRCh38.p7 | 12:113091624 | GCCCTGGGTGTGTAT[A/G]TCTGTGTGTCTGCAC | 1840 |
rs146045861 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | DTX1 | GRCh38.p7 | 12:113070198 | TGAATGAGCTAAACA[C/T]AGCCTGGGGCAGAAA | 1840 |
rs146064417 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | DTX1 | GRCh38.p7 | 12:113065006 | GGGTCCTGGAGGAGG[A/G]TCTCAGGCCTGGGTG | 1840 |
rs146220928 | snp | A/C/T | 0.00125543 | 0.0250231 | missense, utr-variant-3-prime, nc-transcript-variant | DTX1, RASAL1 | GRCh38.p7 | 12:113096734 | TGCGGCTGCTCATCA[A/C/T]GGCCTGGGAGAGAAG | 1840 |
rs146306982 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | DTX1 | GRCh38.p7 | 12:113074981 | AGCTGAGTTCAAGGT[A/G]CCTGTTAAACCTCTC | 1840 |
rs146326583 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | DTX1 | GRCh38.p7 | 12:113070505 | GCCCAGAGAGGAACC[A/G]TTTAGAGGCTGAGGG | 1840 |
rs146418824 | snp | A/C | | | intron-variant | DTX1 | GRCh38.p7 | 12:113078120 | GGTAAGACGGGGCCC[A/C]GGGGGAGGGGGCCTC | 1840 |
rs146520887 | snp | C/T | 0.00412924 | 0.0452501 | synonymous-codon | DTX1 | GRCh38.p7 | 12:113093186 | ACTCCCGGTGAAGAA[C/T]TTGAATGGTACTGGG | 1840 |
rs146713524 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DTX1 | GRCh38.p7 | 12:113066022 | CACAACCGGTGGTAG[C/T]CAGTCCCCAGGACAG | 1840 |
rs146714593 | snp | A/G | 0.000140901 | 0.00839231 | missense | DTX1 | GRCh38.p7 | 12:113077661 | GCCAGACGCGCCGGC[A/G]CCGCCGCCTGCGCCG | 1840 |
rs146731928 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | DTX1 | GRCh38.p7 | 12:113062500 | CTTCCTGAGCTGCAC[A/G]ATAGCAGATGGTGGG | 1840 |
rs146848356 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113083833 | TCTCTCCCCTCCTGG[A/C]CCCAAACAGATCCAG | 1840 |
rs146903282 | in-del | -/TTCTCTTTT | | | intron-variant | DTX1 | GRCh38.p7 | 12:113079511 | TCCCCTCTTGGCCAC[-/TTCTCTTTT]TTTTTTTTTTTTTTT | 1840 |
rs147043615 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | DTX1 | GRCh38.p7 | 12:113094707 | GTGGTCTGCTGCCTA[G/T]GGTGACCCACCAAGG | 1840 |
rs147064415 | snp | A/G | 0.000153988 | 0.00877328 | missense | DTX1 | GRCh38.p7 | 12:113094894 | CGCCTGGGCCGCTGT[A/G]GCCACATGTACCACC | 1840 |
rs147326535 | snp | A/G | 0.000153988 | 0.00877328 | missense | DTX1 | GRCh38.p7 | 12:113058305 | AGCACAGCCGCTGGC[A/G]GCCCTACACGGCCAC | 1840 |
rs147392921 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | DTX1 | GRCh38.p7 | 12:113085454 | GTCATTTAAGTTTCC[A/G]TACCCTTGGTTCTTA | 1840 |
rs147430706 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113076292 | GGCAAAACCCCATCT[C/T]TACTAAAAATACAAA | 1840 |
rs147668204 | snp | G/T | 0.00835141 | 0.0640778 | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | DTX1, RASAL1 | GRCh38.p7 | 12:113098029 | GTCTTTCTCCTCCTC[G/T]CCTGGTCTTTTCCTG | 1840 |
rs147684421 | snp | A/G | 0.000151987 | 0.00871611 | intron-variant | DTX1 | GRCh38.p7 | 12:113094984 | CTGAGGAGTGGGCAG[A/G]GAACGGAGTGGGGTT | 1840 |
rs147740077 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113058699 | CAGTTTCCTCATCTG[C/T]AAAATGGGTAGATCA | 1840 |
rs147845247 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113075453 | TTGAGGGGAAGTCAA[A/G]TGTGCAGCCTTTCTG | 1840 |
rs147951042 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | DTX1, RASAL1 | GRCh38.p7 | 12:113097456 | TGCCTCACCCATTCC[A/G]TGTCATCACCCATGT | 1840 |
rs147968195 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113093281 | AGGAGGCAGCTCCGC[C/G]TGTCACCCGGTGACC | 1840 |
rs148141241 | snp | C/T | 0.0752113 | 0.178743 | intron-variant | DTX1 | GRCh38.p7 | 12:113074182 | TGCAGTGAGCCGAGA[C/T]CACGCCACTGCACTC | 1840 |
rs148265428 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113090959 | TGATGTGAATCAGTA[C/T]GCACGAGTACTTCCC | 1840 |
rs148316726 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | DTX1 | GRCh38.p7 | 12:113085136 | CTCACTGCAACCTCC[A/G]CCTCCCAGGCTCAAG | 1840 |
rs148349628 | in-del | -/TTG | 0.243347 | 0.249911 | intron-variant | DTX1 | GRCh38.p7 | 12:113088840 | GTCTCCTCAAAAGTT[-/TTG]TTGTTGTTGTTGTTG | 1840 |
rs148371487 | in-del | -/GGGGCCCC | | | intron-variant | DTX1 | GRCh38.p7 | 12:113071250 | CAGCTGTGGCTGTGG[-/GGGGCCCC]CCGCCCCCACACCCG | 1840 |
rs148384072 | snp | A/G | 0.000165651 | 0.00909934 | synonymous-codon | DTX1 | GRCh38.p7 | 12:113095092 | CTACGGGGAGAAGAC[A/G]GGTACGCAGCCGCCT | 1840 |
rs148487791 | in-del | -/GAATGGAATG | | | intron-variant | DTX1 | GRCh38.p7 | 12:113080595 | CTTGGAACAGAATGG[-/GAATGGAATG]AATGGAATGGAATGG | 1840 |
rs148542803 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DTX1 | GRCh38.p7 | 12:113070621 | GAGGCACCCACATAC[C/T]CACCTCTAGGCAGTG | 1840 |
rs148592506 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | DTX1 | GRCh38.p7 | 12:113064794 | GTAAGCACTCATGCT[C/T]GAGGAAGAAAAAGAT | 1840 |
rs148609376 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113082641 | GCTCTTATTGCCCAG[C/G]CTGGAGTACAGTGGC | 1840 |
rs148661196 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | DTX1 | GRCh38.p7 | 12:113075146 | GCTGGCAAACGCAGC[A/G]GTCTTCTATTGCATG | 1840 |
rs148943696 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113059454 | GATGTTGATGGTTGC[A/G]TTGGTGGTAATGTGA | 1840 |
rs148965512 | snp | A/G | 3.37758e-05 | 0.00410935 | missense | DTX1 | GRCh38.p7 | 12:113094876 | CGGCCTGAGCTCGTG[A/G]GCCGCCTGGGCCGCT | 1840 |
rs149131822 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113084360 | CATTTATCGAGCGCT[C/T]CCTATGTCCCAGGCT | 1840 |
rs149153679 | snp | A/C | 0.02016 | 0.0983543 | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | DTX1, RASAL1 | GRCh38.p7 | 12:113098215 | GAATGCAGAGGTGAA[A/C]GTGCCCTTCTCTTTC | 1840 |
rs149185734 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DTX1 | GRCh38.p7 | 12:113078774 | CACATGGTGGCTCGA[A/G]CAAGCATCAGCTGCT | 1840 |
rs149206448 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | DTX1 | GRCh38.p7 | 12:113092539 | TCATTTGAAGAGAGG[A/G]TAGTACCTTGTCACA | 1840 |
rs149307886 | snp | G/T | 0.00835141 | 0.0640778 | intron-variant, downstream-variant-500B | DTX1, RASAL1 | GRCh38.p7 | 12:113096138 | TGAACTCAGGAAGCA[G/T]AGGTTGCACTGAGTC | 1840 |
rs149466779 | snp | A/T | 0.000153988 | 0.00877328 | missense | DTX1 | GRCh38.p7 | 12:113058438 | GTCCATGCACCAGTT[A/T]CGCCAGGACACAGGT | 1840 |
rs149468438 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113060291 | AGGGAGCAAGACAAA[A/G]TCATCAGTCGAGGTC | 1840 |
rs149588946 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | DTX1 | GRCh38.p7 | 12:113075092 | CGGTATTTATCTCAA[C/T]TGATCCTCTCAGCAA | 1840 |
rs149645873 | snp | C/G | 0.0182019 | 0.0936463 | intron-variant | DTX1 | GRCh38.p7 | 12:113070021 | GAGACTAAGTCAGAG[C/G]GAACAGCAAATGAAG | 1840 |
rs149657393 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | DTX1 | GRCh38.p7 | 12:113087329 | GAGGTTTGTCTAGGC[A/G]GACGGAGGTGCTGGG | 1840 |
rs149938685 | snp | A/C/G | 0.0883596 | 0.190715 | intron-variant | DTX1 | GRCh38.p7 | 12:113066467 | CGGGAGGTGGAGGTA[A/C/G]CAGTGAGCTGAGATT | 1840 |
rs149995032 | snp | G/T | 0.0126979 | 0.078662 | intron-variant | DTX1 | GRCh38.p7 | 12:113062350 | CAGCATAGACAATAT[G/T]TAAGTGAATGCGTGT | 1840 |
rs150027646 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113092177 | ACACCAGGACTTAGT[A/G]CCTGGGAAGCAAAGA | 1840 |
rs150097358 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DTX1 | GRCh38.p7 | 12:113063436 | TAACTCAGCCACTTC[C/T]GCAGAAGCTCCCAGC | 1840 |
rs150127864 | snp | C/G | 0.00184404 | 0.0303088 | intron-variant | DTX1 | GRCh38.p7 | 12:113095313 | AAATCCCTGTACTGT[C/G]CCTCTCTGCAGGGCC | 1840 |
rs150186375 | snp | A/T | 0.00795532 | 0.062565 | intron-variant | DTX1 | GRCh38.p7 | 12:113090009 | AGAGCTGTACTGAGG[A/T]CTCTGCTAAGCTTGA | 1840 |
rs150200049 | snp | C/T | 7.23458e-05 | 0.00601396 | missense | DTX1 | GRCh38.p7 | 12:113094092 | AGGTGAAAAACCCAC[C/T]TGATGAGGTGAGGAG | 1840 |
rs150479893 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | DTX1 | GRCh38.p7 | 12:113084304 | AGAGTTTCCACCCCA[C/T]GTGGTGGGTGGGAGG | 1840 |
rs150588209 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DTX1 | GRCh38.p7 | 12:113086572 | ATGCTGAGCATAGAC[C/T]GCAGTGGGGCTGAAG | 1840 |
rs150639460 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | DTX1 | GRCh38.p7 | 12:113080952 | TGCACTGCAGCCTGA[A/G]AGACAGAGCAAGACA | 1840 |
rs150657141 | snp | C/T | 0.00159617 | 0.0282053 | utr-variant-3-prime, nc-transcript-variant | DTX1, RASAL1 | GRCh38.p7 | 12:113097328 | TCCCCATCTGTGTCT[C/T]AGTTGCATCTGTACA | 1840 |
rs150707859 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DTX1 | GRCh38.p7 | 12:113091221 | TCTGTGTGTATGTGT[A/G]TGTCCCCGTGTGTGC | 1840 |
rs151073350 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113059727 | GATGACAGAACCACA[C/T]GTAATAACCCCAGGC | 1840 |
rs151113017 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | DTX1 | GRCh38.p7 | 12:113089733 | GATGGGTAAATAAAT[A/G]ACAGTCCCACAGTGA | 1840 |
rs151165215 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | DTX1 | GRCh38.p7 | 12:113083029 | ACGGTGTCACAGGGT[A/G]GTTTCCTTCTGAGGC | 1840 |
rs151237120 | snp | C/T | 0.000153988 | 0.00877328 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant | DTX1, RASAL1 | GRCh38.p7 | 12:113096876 | CCCGGACGCTAGCTA[C/T]CTAGACAACGTGCTG | 1840 |
rs180815241 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | DTX1 | GRCh38.p7 | 12:113070433 | ACTGAGATCACTTCC[C/T]TCCGGGAAGCCACCC | 1840 |
rs180934768 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113088756 | AGCACTTTGGGAGGT[C/T]GAGGAGGGAGGACTA | 1840 |
rs180958661 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113063069 | GTCGCTTGCTCGCTT[A/C/T]GCAGTACTGAGCCAA | 1840 |
rs180994281 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | DTX1 | GRCh38.p7 | 12:113076266 | GAGTTCGAGACCAGC[C/T]TGGCCAACATGGCAA | 1840 |
rs181092674 | snp | C/T | 0.000140726 | 0.00838709 | intron-variant | DTX1 | GRCh38.p7 | 12:113093988 | TCTGAGCCAAGCCTT[C/T]GGGGACAGACTCTGG | 1840 |
rs181097917 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113081277 | GAGGTTGCAGTGAGC[C/T]GAGATCACGCCACTG | 1840 |
rs181169945 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DTX1 | GRCh38.p7 | 12:113071429 | ACACAAAAACAGGCC[A/G]AGGCAGAGGCACGGA | 1840 |
rs181578992 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | DTX1 | GRCh38.p7 | 12:113086929 | CCCCACCCTGCCCCC[A/C]ACCTGAAGCACTTCC | 1840 |
rs181587878 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DTX1 | GRCh38.p7 | 12:113060965 | CCACAAGGCTGCCAA[A/G]TTGGCAACTTTACCT | 1840 |
rs181690150 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DTX1 | GRCh38.p7 | 12:113082249 | TGCCCAGCCTCACTC[C/T]AGCCCCTCTAACTGA | 1840 |
rs181707615 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB | DTX1 | GRCh38.p7 | 12:113055206 | GAAGTCCAGAGACAC[A/G]AGTTCTTCTTTCCAA | 1840 |
rs181792478 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113076821 | CAGATTGATGAATGA[A/C]TCATTGAATGAGTGA | 1840 |
rs181861204 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113069703 | GTCTTCTTAGGGAGC[C/T]TCAGTCTCCCCATCT | 1840 |
rs181992374 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DTX1 | GRCh38.p7 | 12:113087859 | TTTGGAGGAGGGAGG[A/G]GACTTGGCTGCCCTA | 1840 |
rs182108797 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113092628 | GAAAACCTGGACTTA[C/T]CATTGTTAATGATAT | 1840 |
rs182277164 | snp | G/T | 0.00914312 | 0.0669923 | intron-variant | DTX1 | GRCh38.p7 | 12:113062202 | ACTTTGAGGGGAGAC[G/T]GCCCTAGCTTTGCTA | 1840 |
rs182406602 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | DTX1 | GRCh38.p7 | 12:113082839 | CTGGCCTCAAGCATC[C/T]GCCTGCCTCAGCCTC | 1840 |
rs182414225 | snp | G/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, utr-variant-5-prime | DTX1 | GRCh38.p7 | 12:113057762 | GGCTGGCTGAGAGCC[G/T]CAGGAGCAGCAGGCT | 1840 |
rs182456277 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113059201 | GATGGATGATGGTGA[C/T]GTGGCAGTGTTGGTG | 1840 |
rs182544272 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | DTX1 | GRCh38.p7 | 12:113079902 | ACCTGGGACGAGTCC[C/G]TCTCCTTCCTTGAGC | 1840 |
rs182558678 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113089696 | GCTGGAGACTACCTC[A/G]GGACTGTCCCCCAGG | 1840 |
rs182911752 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | DTX1, RASAL1 | GRCh38.p7 | 12:113096396 | AGTGAGCTCTGGTTG[C/T]ACTGCTGCACTCCAG | 1840 |
rs183039952 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | DTX1 | GRCh38.p7 | 12:113084325 | GGGTGGGAGGACAGT[G/T]ATAGCTGCGGGCCTA | 1840 |
rs183049430 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113064936 | TGTGATTTGGGTAAA[C/T]AGAATGATAGGAGGA | 1840 |
rs183059169 | snp | A/C | | | utr-variant-5-prime | DTX1 | GRCh38.p7 | 12:113058072 | GAACCCAGAGTTAGA[A/C]AGGAGGCCAGACGGT | 1840 |
rs183267714 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | DTX1 | GRCh38.p7 | 12:113078217 | AATAATAATAATGAC[A/G]ATAAGTAATATCCAG | 1840 |
rs183388902 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | DTX1 | GRCh38.p7 | 12:113095755 | CAGGTTGTCTGATTT[A/G]ACTTTCTGCTTTTCA | 1840 |
rs183399927 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | DTX1 | GRCh38.p7 | 12:113074301 | CTCAGAGGACAGCAA[C/T]AGGAGGGCTGCACTT | 1840 |
rs183552965 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | DTX1 | GRCh38.p7 | 12:113072450 | GATGAATAGGAGTTT[G/T]CCAAGTGAACAAGGG | 1840 |
rs183809326 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113089969 | GGTAGCAAACTGGCT[A/G]TACTGATTGATAGAG | 1840 |
rs183848543 | snp | C/T | 0.000472478 | 0.0153628 | missense | DTX1 | GRCh38.p7 | 12:113094879 | CCTGAGCTCGTGGGC[C/T]GCCTGGGCCGCTGTG | 1840 |
rs183905882 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | DTX1 | GRCh38.p7 | 12:113065708 | TGTGGAGGGGATGGT[G/T]AAGAAGGTGGTAAGG | 1840 |
rs183927822 | snp | G/T | 0.00159617 | 0.0282053 | upstream-variant-2KB | DTX1 | GRCh38.p7 | 12:113056041 | CAGTTGTTTGCAGGT[G/T]GCTGTGAATGACATG | 1840 |
rs183944794 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113090901 | ATGTGCGCATGTGTC[C/T]TCGTGTGCAGTGAGT | 1840 |
rs183961753 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | DTX1 | GRCh38.p7 | 12:113067722 | GAAATCTGGACTGGT[A/G]TGAATCTGCCCCAAT | 1840 |
rs184086340 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113086526 | TGTGTTGGGAGAGAC[A/G]GGTGGGACTGTTTTA | 1840 |
rs184099158 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | DTX1 | GRCh38.p7 | 12:113082627 | AGAGACAGAGCCTCG[C/T]TCTTATTGCCCAGGC | 1840 |
rs184105592 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | DTX1 | GRCh38.p7 | 12:113060318 | GGTCTTGTGCTGGAG[A/G]ACCTACACTGAAGGT | 1840 |
rs184387416 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113087302 | GGGGACACTGAAGCC[C/T]AGAGAAGCTCAGAGG | 1840 |
rs184511100 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | DTX1 | GRCh38.p7 | 12:113080536 | GACTGGAAATCAGAA[C/G]GTTAAAAGAAAAAAA | 1840 |
rs184634749 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | DTX1 | GRCh38.p7 | 12:113080493 | TGAGAACCTTCTCTC[C/T]GGGTAAATTTATTGT | 1840 |
rs184777281 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | DTX1, RASAL1 | GRCh38.p7 | 12:113097853 | TGGGCAGTGGGGTGG[C/T]TAATTGTCTTCGGCC | 1840 |
rs184823931 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113074644 | GTGATCTGACTTGCA[C/T]TGAGCAGGATCCCTC | 1840 |
rs184870037 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113069063 | CCTGCCCCAGTCATT[C/T]TGTGGCTGAAGAGTT | 1840 |
rs184914838 | snp | C/T | 8.77308e-05 | 0.00662252 | intron-variant | DTX1 | GRCh38.p7 | 12:113093704 | ACCTTAAAAAGAGTA[C/T]GCCCTCCACGCCCTG | 1840 |
rs184927903 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113070497 | CTGGCCCAGCCCAGA[A/G]AGGAACCGTTTAGAG | 1840 |
rs184978236 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113092032 | CCTTCAGTCCTCCCA[A/G]CGACTATAAGTGAGG | 1840 |
rs185340479 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DTX1 | GRCh38.p7 | 12:113075074 | GAATCATCAGAGTAG[A/G]CACGGTATTTATCTC | 1840 |
rs185442639 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | DTX1, RASAL1 | GRCh38.p7 | 12:113097236 | TGTTGAACTCATGCA[C/T]GCACACCCACGTGCC | 1840 |
rs185444756 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113061415 | CCCAGGAGCAAAACA[A/G]TGTCAAGAAAGGACG | 1840 |
rs185448999 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DTX1 | GRCh38.p7 | 12:113089536 | CCGCAGGCAGCGGTC[A/G]CTTGTCCAGGCAGGA | 1840 |
rs185457075 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | DTX1 | GRCh38.p7 | 12:113092680 | GAGCCTTTAATATGC[C/T]CAGATATGTTGTGAA | 1840 |
rs185468961 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113064380 | TGTTTTGAAACTAAA[G/T]TCATCGCTCGTATTT | 1840 |
rs185558649 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113059013 | CTATACTGGCTCCAA[A/G]TGTTGGTTTGTGGGG | 1840 |
rs185612026 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | DTX1 | GRCh38.p7 | 12:113070225 | GAAAAGTGTGCTCTC[C/T]GAGTGTGGATGGCTG | 1840 |
rs185694008 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | DTX1 | GRCh38.p7 | 12:113085636 | CCCTTTGTCTCCCAT[C/T]TTTTCTGTAGTTTGC | 1840 |
rs185765794 | snp | C/G/T | 0.00517822 | 0.0506191 | intron-variant | DTX1 | GRCh38.p7 | 12:113081373 | AAAGCTACTGTTCTA[C/G/T]AGGAGGCTGAAAATT | 1840 |
rs185775187 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113082631 | ACAGAGCCTCGCTCT[G/T]ATTGCCCAGGCTGGA | 1840 |
rs185776357 | snp | C/T | 0.00199481 | 0.0315187 | upstream-variant-2KB | DTX1 | GRCh38.p7 | 12:113055147 | TCAGGAAAGGCTTCC[C/T]GGAGGAGGTGACATT | 1840 |
rs185901469 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | DTX1 | GRCh38.p7 | 12:113056239 | ATCGCTCTAAGCTTT[C/T]GTGATCCTGGGCCTG | 1840 |
rs185928605 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | DTX1 | GRCh38.p7 | 12:113076883 | GGCCTATGTGCATGG[C/T]CTTGGTCTCTGTCTA | 1840 |
rs186337550 | snp | A/G | 0.00318978 | 0.0398085 | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | DTX1, RASAL1 | GRCh38.p7 | 12:113098237 | TTCTCTTTCACAAGA[A/G]CACAAGGCAATGCAC | 1840 |
rs186393191 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113072233 | CAGGCTTTGTGCCTG[A/G]TGCTCCAAACATAGT | 1840 |
rs186417812 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | DTX1 | GRCh38.p7 | 12:113076494 | TGGGGCCGGTCATGG[C/T]GGCTCACACCTGTCA | 1840 |
rs186432196 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | DTX1 | GRCh38.p7 | 12:113082492 | GGGAAAGGGATGGAG[A/G]TGGGGGGTCTTTGAG | 1840 |
rs186543234 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113078364 | CACAGATGAAGAACT[A/G]ACTCCCCCAAGATCA | 1840 |
rs186617475 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | DTX1 | GRCh38.p7 | 12:113094432 | AATATATGGGAAGGG[G/T]CTGGGTGCAGTGGCT | 1840 |
rs186681234 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | DTX1 | GRCh38.p7 | 12:113074349 | CACCTGTAAGAAAGA[A/C]GGGAGGAAATGATGA | 1840 |
rs186685721 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | DTX1, RASAL1 | GRCh38.p7 | 12:113096220 | AAAAAAAAAAACAGG[C/T]AGGCCAAGCGCAGTG | 1840 |
rs186832175 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113091072 | GAGCGCATGCTCCTC[C/T]GGGTTTGCTGCCCAC | 1840 |
rs187106856 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | DTX1 | GRCh38.p7 | 12:113055557 | CCTCTCTCTTTAGTC[C/T]ACAGCAGGTGAAAGC | 1840 |
rs187120991 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113068872 | GGCTGACAGTGGAAG[C/T]CGGGGAAGTTCAAAT | 1840 |
rs187143054 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113083826 | CCCTCCTTCTCTCCC[C/G]TCCTGGACCCAAACA | 1840 |
rs187156067 | snp | A/C/G | 0.000399281 | 0.0141238 | utr-variant-5-prime | DTX1 | GRCh38.p7 | 12:113057935 | TGTTTCCTCCGGCAT[A/C/G]AGAGAGACACTTGCT | 1840 |
rs187270662 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113062552 | AGGTTCACTGACCCC[G/T]GCCCCACATGTTCTG | 1840 |
rs187455334 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113088134 | CGGAAACTCCAGGAC[C/G]CAGTGCCAGCTGCAC | 1840 |
rs187506105 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | DTX1 | GRCh38.p7 | 12:113086044 | AGGCTAAGGTGGGAG[A/G]ATCACTTGAGCCCAG | 1840 |
rs187881214 | snp | C/G/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113072926 | GGGCCAGGCTGGTCC[C/G/T]GAATTCCTGACCTCA | 1840 |
rs188007443 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113075899 | ACCTGCTGTGTGCAG[A/G]TGCTGGGGATATAGC | 1840 |
rs188013302 | snp | C/G/T | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | DTX1, RASAL1 | GRCh38.p7 | 12:113097941 | ACGGTGGGAGTCAGC[C/G/T]AAGATTTAAAGGGAT | 1840 |
rs188094492 | snp | G/T | 0.00914312 | 0.0669923 | intron-variant | DTX1 | GRCh38.p7 | 12:113074667 | GATCCCTCTGGCTGC[G/T]GTATGGGAAATGGAT | 1840 |
rs188181710 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113089898 | AACTCCTAGACCAAA[C/G]ACTCAGCAAGAGCAG | 1840 |
rs188237382 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | DTX1 | GRCh38.p7 | 12:113079233 | GAAAAGACCAGGGGG[A/G]TTTGGACTGTGGTCC | 1840 |
rs188363778 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, utr-variant-3-prime, nc-transcript-variant | DTX1, RASAL1 | GRCh38.p7 | 12:113096520 | CAAACATAAGTAACT[C/T]GGAAAGAGCTTTTAC | 1840 |
rs188469192 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | DTX1 | GRCh38.p7 | 12:113065468 | GGGGGTGGGGATGCC[C/T]GGGACAGACCCCCTC | 1840 |
rs188742565 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DTX1 | GRCh38.p7 | 12:113095567 | ACCACAGCCACCTCC[C/T]TCACACATCTTATCT | 1840 |
rs188744449 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113058962 | GATTTAAACCCAGGC[A/G]GTTGAGTTCCAGAAC | 1840 |
rs188783636 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113060464 | TGATGTTTGAACAGA[G/T]ATCTGAAGAATGAGT | 1840 |
rs188902523 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113066161 | GGGCCTGGAACCTGG[A/T]AACAGCTACCTCGGG | 1840 |
rs188924683 | snp | C/G | 0.00119737 | 0.0244387 | upstream-variant-2KB | DTX1 | GRCh38.p7 | 12:113055154 | AGGCTTCCTGGAGGA[C/G]GTGACATTTAATCAG | 1840 |
rs188971192 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | DTX1, RASAL1 | GRCh38.p7 | 12:113097402 | CCTGCCAGGGCTCGG[A/G]GGGCAAAGAGGGACT | 1840 |
rs188980900 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113075620 | GCTGTCAGGGGAGCA[C/T]GCAGAGCTTTGGCAA | 1840 |
rs189014577 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | DTX1 | GRCh38.p7 | 12:113081513 | GATGGGGAGACAGAC[C/G]TACAGCAAGCAAAGA | 1840 |
rs189015405 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | DTX1 | GRCh38.p7 | 12:113085210 | GCACGCCACCAACCC[A/G]GCTAATTTTTTATAT | 1840 |
rs189174398 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | DTX1 | GRCh38.p7 | 12:113090292 | ATTCCTATAAAAGTA[C/T]AGAGAGGGAGGAAGT | 1840 |
rs189335369 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113059699 | GGTTTGGGGAAGTTC[C/T]TATGAATCCCTGGAT | 1840 |
rs189487330 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113081042 | TTAATAGGTTGCGAG[G/T]TGAAATGAATTTCTT | 1840 |
rs189500485 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | DTX1 | GRCh38.p7 | 12:113092932 | AGGTGTCTGCACTAA[A/C]GTCTAAGGGTGCATC | 1840 |
rs189521168 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113070264 | ATGACTTCTGGGTTG[A/G]TGAAGGATTCAGTGA | 1840 |
rs189653920 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113062949 | ACTGGAGCCCCTCCA[C/T]GGGGAGGCCTAATGC | 1840 |
rs189716744 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DTX1 | GRCh38.p7 | 12:113070852 | CACCCTCCCAAGAGT[C/T]CACCTCTCCGGGCCT | 1840 |
rs189718773 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DTX1 | GRCh38.p7 | 12:113093803 | TAGCATTTACTACCT[C/T]ACCTCCATTGCCTGA | 1840 |
rs189778686 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DTX1 | GRCh38.p7 | 12:113076675 | AAGGAAAGAATCAAT[A/G]AATGAATGAATCATT | 1840 |
rs189801014 | snp | A/C | | | upstream-variant-2KB, intron-variant | DTX1 | GRCh38.p7 | 12:113056954 | GAGGCGGTGAGAACG[A/C]GGGTGCTTAGGGACC | 1840 |
rs189862336 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113092349 | AAAAAAGGTACCATA[C/T]TGTCCCCATTTTACA | 1840 |
rs190005281 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113061949 | GGCCTCAAGTGAGCC[A/G]CCCGCCTCGGCCTCC | 1840 |
rs190012361 | snp | A/G | | | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | RASAL1, DTX1 | GRCh38.p7 | 12:113098392 | GGACCCTGTCCTTGG[A/G]GAGGAGGGTCAGGTT | 1840 |
rs190106972 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113069527 | CACAAGGAAACCACT[A/T]ATGGGCCACAGCTTA | 1840 |
rs190259243 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113087576 | CTCACACCCCTAGAA[A/G]GGAGAAAGGGAGAGG | 1840 |
rs190262546 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | DTX1 | GRCh38.p7 | 12:113089605 | CATCAAAAGGGGGCC[A/G]GGTGGCTCCCACGCT | 1840 |
rs190275054 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113064404 | CGTATTTGGTAGTCA[A/T]TGGTGGCTTCTCAGT | 1840 |
rs190645916 | snp | A/C | 0.381023 | 0.212915 | missense | DTX1 | GRCh38.p7 | 12:113078027 | CCGGCGGAGCGCGCA[A/C]CCCGGGGCAGAACAA | 1840 |
rs190711940 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113088194 | TCATTTCCCTTCTCT[A/G]GGCTTCAGTCCCATC | 1840 |
rs190881947 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | DTX1 | GRCh38.p7 | 12:113095583 | TCACACATCTTATCT[A/C]GTTTCCTGAGCCACT | 1840 |
rs190949135 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113078456 | ATTATTTGCTAAACC[A/C]GTTATATGTATCACC | 1840 |
rs191126342 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113082651 | CCCAGGCTGGAGTAC[A/G]GTGGCGCAATCACAG | 1840 |
rs191337509 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113066327 | TGAGGTCAGGAGTTC[A/G]AGACCAGCCTGGCCA | 1840 |
rs191415574 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | DTX1 | GRCh38.p7 | 12:113090789 | TGTGTGTGCGCTGCA[C/T]CTGTGTGCATGTGTG | 1840 |
rs191477584 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DTX1 | GRCh38.p7 | 12:113059952 | AACATTGCATTGTTG[C/T]AGAAAGTTCTATTAC | 1840 |
rs191495345 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113094445 | GGGCTGGGTGCAGTG[A/G]CTCATCCCTGTAGTT | 1840 |
rs191499320 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | DTX1, RASAL1 | GRCh38.p7 | 12:113096373 | GGAGCCCAGGAGTTC[A/G]AGGCTGCAGTGAGCT | 1840 |
rs191565505 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113086214 | CAGTGAGCCAAGATC[A/G]AGCCACTGCACTCCA | 1840 |
rs191633920 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | DTX1 | GRCh38.p7 | 12:113091211 | TGTGTGTGCTTCTGT[A/G]TGTATGTGTGTGTCC | 1840 |
rs191640094 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113068968 | GCTTCACCTCTCTGT[A/G]CTTCACTCAGTGTTT | 1840 |
rs191666959 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | DTX1 | GRCh38.p7 | 12:113065504 | CCTCTCCCTCTCCTT[C/T]TCCTCCCCTCACCCC | 1840 |
rs191764283 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113072407 | GAAGCCCATGTTGGA[A/G]GAGATGAGCACATGG | 1840 |
rs191962829 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | DTX1 | GRCh38.p7 | 12:113089949 | TGGGCATTATATAGA[C/T]CTGGGGTAGCAAACT | 1840 |
rs191987395 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | DTX1 | GRCh38.p7 | 12:113084214 | CCTGCGGGGGTGGGG[A/G]AGATCCGCCCTGTCC | 1840 |
rs192011491 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime | DTX1 | GRCh38.p7 | 12:113057980 | CCTTTATCGGAGAAG[A/G]CTCTACAGGGAAGGG | 1840 |
rs192109884 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | DTX1 | GRCh38.p7 | 12:113082626 | TAGAGACAGAGCCTC[A/G]CTCTTATTGCCCAGG | 1840 |
rs192152052 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113080410 | AGTGGGTCCTAGAAT[A/G]ACAGGCTAGGGGGAG | 1840 |
rs192305353 | snp | A/C | 0.00517822 | 0.0506191 | utr-variant-3-prime, nc-transcript-variant | DTX1, RASAL1 | GRCh38.p7 | 12:113097836 | TTCCCTTTCGTTGGG[A/C]GTGGGCAGTGGGGTG | 1840 |
rs192318409 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113075784 | AATGAAGGAATGGAC[A/G]AATGCAGGGATGAGC | 1840 |
rs192387918 | snp | G/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113074578 | GGCAAGGACTTTGGC[G/T]TTTACTCCAAGTGAG | 1840 |
rs192495094 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | DTX1 | GRCh38.p7 | 12:113055929 | ATCCAGCTTGCTGGA[A/G]GACAGGGGGACTGGC | 1840 |
rs192566979 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DTX1 | GRCh38.p7 | 12:113079855 | TGAGCCACCATGCCC[A/G]GCCCCCTTCTTGACC | 1840 |
rs192707207 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113080514 | AATTTATTGTAACCC[A/G]CAAGAAGACTGGAAA | 1840 |
rs192893464 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | DTX1, RASAL1 | GRCh38.p7 | 12:113097080 | TCAGGGGACCTGCCT[A/G]GTGGCAGCTGGGATG | 1840 |
rs193019994 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113085431 | AAGCTGATAATTCCT[A/G]AAGAGACGTCATTTA | 1840 |
rs193153906 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113074868 | AGGATGAGACCAAGA[C/T]TTGGGGGTCCAAGGA | 1840 |
rs199645925 | snp | A/G | 0.00297454 | 0.0384503 | intron-variant | DTX1 | GRCh38.p7 | 12:113093234 | GGCAGGTGAGGTCTG[A/G]CCCAGGGCGGGAAAG | 1840 |
rs199882931 | snp | A/C/G | 6.66744e-05 | 0.00577345 | missense, utr-variant-3-prime, nc-transcript-variant | DTX1, RASAL1 | GRCh38.p7 | 12:113096829 | ATCCACCACAAGACC[A/C/G]AGTTTGGATCCAACC | 1840 |
rs199883523 | snp | A/C/G/T | 0.000299905 | 0.0122424 | intron-variant | DTX1 | GRCh38.p7 | 12:113094118 | AGGAGGGGATGGGGG[A/C/G/T]GCTGGGGGAGGGCCC | 1840 |
rs199944169 | snp | C/T | 3.32408e-05 | 0.00407668 | missense | DTX1 | GRCh38.p7 | 12:113058323 | CCTACACGGCCACCG[C/T]GTGCCACCACATTGA | 1840 |
rs200095694 | snp | C/T | 0.000511024 | 0.0159766 | intron-variant | DTX1 | GRCh38.p7 | 12:113095288 | CCCTGCCACCACCTG[C/T]TCATGGTCTAAATCC | 1840 |
rs200220437 | snp | A/C/G | 1.66007e-05 | 0.00288098 | missense | DTX1 | GRCh38.p7 | 12:113058358 | GTGCTGAAGGAGGAC[A/C/G]CTCGCGGTTCCGTGG | 1840 |
rs200235649 | in-del | -/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113059024 | CCAAGTGTTGGTTTG[-/T]GGGGTGGAGTCGTGC | 1840 |
rs200317078 | snp | C/G/T | 3.9065e-05 | 0.00441942 | intron-variant | DTX1 | GRCh38.p7 | 12:113077395 | CCAACGCCCGCTGTG[C/G/T]TGACGCCTCCTCCCC | 1840 |
rs200332302 | snp | C/G | 0.0002318 | 0.0107632 | missense | DTX1 | GRCh38.p7 | 12:113077551 | CATCTGCATCACCAT[C/G]CAGAACGCCTACGAG | 1840 |
rs200357238 | snp | A/C/G | 0.00152241 | 0.0275484 | intron-variant, utr-variant-3-prime, nc-transcript-variant | DTX1, RASAL1 | GRCh38.p7 | 12:113096707 | CCACTGTGTCCCTGT[A/C/G]CCCCCAGGTGCTGCG | 1840 |
rs200434970 | in-del | -/A | | | intron-variant | DTX1 | GRCh38.p7 | 12:113061210 | TTTGCCGGAAAAGGG[-/A]AAAAAAAACACTCAT | 1840 |
rs200546916 | snp | A/G/T | 0.00233806 | 0.0341129 | synonymous-codon | DTX1 | GRCh38.p7 | 12:113077683 | CCTGCGCCGCCGCCT[A/G/T]GACCTCGCCTACCCG | 1840 |
rs200652619 | snp | A/G | 5.28546e-05 | 0.00514048 | missense, utr-variant-3-prime, nc-transcript-variant | DTX1, RASAL1 | GRCh38.p7 | 12:113096913 | CTCACAGCCCAGGGC[A/G]TATCCGAGGCTGCAG | 1840 |
rs200694655 | snp | C/T | 0.000399281 | 0.0141238 | missense | DTX1 | GRCh38.p7 | 12:113094091 | AAGGTGAAAAACCCA[C/T]CTGATGAGGTGAGGA | 1840 |
rs200751640 | snp | A/G | 0.00199802 | 0.0315439 | missense, utr-variant-3-prime, nc-transcript-variant | DTX1, RASAL1 | GRCh38.p7 | 12:113096808 | GACACCGTGGTGTGG[A/G]ACGAGATCCACCACA | 1840 |
rs200824699 | snp | C/T | 1.8945e-05 | 0.00307768 | missense | DTX1 | GRCh38.p7 | 12:113058221 | GCCACGGTGGGCTGA[C/T]GCCTGTGAATGGTCT | 1840 |
rs201023177 | in-del | -/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113087144 | AGTGACCCCCGCAGC[-/T]CCCCATACCTCTAGA | 1840 |
rs201096784 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113058456 | CCAGGACACAGGTGA[A/G]CAGACACCCACCCCA | 1840 |
rs201111193 | snp | C/T | 0.00250164 | 0.0352784 | synonymous-codon | DTX1 | GRCh38.p7 | 12:113077677 | CCGCCGCCTGCGCCG[C/T]CGCCTGGACCTCGCC | 1840 |
rs201136362 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113066718 | CCTACTGTGTGCCAG[A/G]CACTGTCCGGGCACT | 1840 |
rs201152569 | snp | A/C | 0.00399202 | 0.044498 | missense | DTX1 | GRCh38.p7 | 12:113077630 | ATCTACTTCAACAGC[A/C]TGTCGCAGATGAACC | 1840 |
rs201346405 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113061708 | TAAATCTTTTTTTTT[C/T]CTTCTTTTTTTGAGA | 1840 |
rs201380111 | snp | A/G | 4.9807e-05 | 0.00499009 | missense | DTX1 | GRCh38.p7 | 12:113058364 | AAGGAGGACGCTCGC[A/G]GTTCCGTGGTCCTGG | 1840 |
rs201473015 | snp | A/G | 0.00199799 | 0.0315437 | missense | DTX1 | GRCh38.p7 | 12:113094862 | GGCACAAGGGCGTGC[A/G]GCCTGAGCTCGTGGG | 1840 |
rs201480494 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113079513 | CCCTCTTGGCCACTT[C/T]TCTTTTTTTTTTTTT | 1840 |
rs201609570 | snp | A/G | 1.75517e-05 | 0.00296236 | intron-variant | DTX1 | GRCh38.p7 | 12:113093705 | CCTTAAAAAGAGTAC[A/G]CCCTCCACGCCCTGC | 1840 |
rs201619192 | snp | A/G | 1.65985e-05 | 0.00288079 | synonymous-codon | DTX1 | GRCh38.p7 | 12:113058345 | CCACATTGAGAACGT[A/G]CTGAAGGAGGACGCT | 1840 |
rs201749394 | snp | C/G | 5.88287e-05 | 0.00542318 | intron-variant, utr-variant-3-prime, nc-transcript-variant | DTX1, RASAL1 | GRCh38.p7 | 12:113096701 | CCGGCCCCACTGTGT[C/G]CCTGTCCCCCCAGGT | 1840 |
rs201802722 | snp | A/C | 0.000288951 | 0.0120163 | synonymous-codon | DTX1 | GRCh38.p7 | 12:113077524 | CGGCGCATGGACGGC[A/C]TACGATATGGACATC | 1840 |
rs201809063 | snp | A/G/T | 0.000134572 | 0.0082018 | missense | DTX1 | GRCh38.p7 | 12:113094858 | CTTCGGCACAAGGGC[A/G/T]TGCGGCCTGAGCTCG | 1840 |
rs201834487 | in-del | -/CTGACCTC | | | intron-variant | DTX1 | GRCh38.p7 | 12:113085276 | GTTGGTCTCCAACTC[-/CTGACCTC]AAGCAATCCACCCAC | 1840 |
rs201845055 | snp | A/G | 1.65611e-05 | 0.00287755 | missense | DTX1 | GRCh38.p7 | 12:113077543 | GATATGGACATCTGC[A/G]TCACCATCCAGAACG | 1840 |
rs201857844 | snp | A/G | 0.000132218 | 0.00812968 | synonymous-codon | DTX1 | GRCh38.p7 | 12:113095140 | CCTCATCCCCCACTC[A/G]CTGCCCGGCTTCCCT | 1840 |
rs201878530 | snp | G/T | 3.35137e-05 | 0.00409338 | missense | DTX1 | GRCh38.p7 | 12:113058293 | AGTGGCTGAATGAGC[G/T]CAGCCGCTGGCGGCC | 1840 |
rs201893507 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | DTX1, RASAL1 | GRCh38.p7 | 12:113097190 | CCAAAAAGACAGAGA[C/T]CCGCCCCCTCACACA | 1840 |
rs202121236 | in-del | -/AGG | 0.0437281 | 0.141251 | intron-variant | DTX1 | GRCh38.p7 | 12:113089548 | GTCGCTTGTCCAGGC[-/AGG]AGGATGTTCTCACTG | 1840 |
rs202125642 | snp | G/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113066245 | GAATCATGGGGTGTG[G/T]AGGCCGGGTGTGGTG | 1840 |
rs202200189 | snp | C/T | 3.29614e-05 | 0.00405951 | intron-variant | DTX1 | GRCh38.p7 | 12:113095310 | TCTAAATCCCTGTAC[C/T]GTCCCTCTCTGCAGG | 1840 |
rs207473376 | snp | A/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113082974 | AAACCACAGAAATGT[A/T]TTCTCTCTTTCACAT | 1840 |
rs207473377 | snp | A/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113086094 | ACAACATAGTGAGAC[A/T]CCACCTTTACAAAAT | 1840 |
rs367610635 | in-del | -/AGGA | | | intron-variant | DTX1 | GRCh38.p7 | 12:113087500 | CAGGACTGTGGGGGG[-/AGGA]GGGGGAGAAGGCAGC | 1840 |
rs367624510 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113082889 | AGGCGTGAGCCACAG[C/T]GACTGGCCTGTCTCT | 1840 |
rs367688130 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113068306 | GGGGCTGCCAGGCCC[A/G]AAGGAACACAGACAC | 1840 |
rs367890116 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113075933 | AAATAAAACAAAATC[C/T]CTGACCTTGTGGCTA | 1840 |
rs368097273 | snp | A/C | 0.0126979 | 0.078662 | upstream-variant-2KB | DTX1 | GRCh38.p7 | 12:113055886 | CAGGTGGTCCACCCC[A/C]CTCCCAGCCAATGTG | 1840 |
rs368121992 | in-del | -/GT | | | intron-variant | DTX1 | GRCh38.p7 | 12:113091247 | TGTGCACAAGTCTCT[-/GT]ATGTAGGTGTGGGGA | 1840 |
rs368312235 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113087482 | GCCCCAGGCTGTGTT[C/T]CCCAGGACTGTGGGG | 1840 |
rs368350982 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113062762 | CGGAAGAAAGCCCCG[A/G]TGTCAGGCTGGGGCC | 1840 |
rs368358830 | snp | A/G | | | upstream-variant-2KB | DTX1 | GRCh38.p7 | 12:113055565 | TTTAGTCTACAGCAG[A/G]TGAAAGCAAGCAGAA | 1840 |
rs368422025 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | DTX1 | GRCh38.p7 | 12:113087081 | CCATCTCCTCCCGTT[C/T]CTTCCCCCGCAGAGA | 1840 |
rs368482500 | snp | G/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113069587 | GGGAAACAGAACACT[G/T]CGGGATTATTGATCA | 1840 |
rs368498328 | snp | A/G/T | 6.74745e-05 | 0.00580804 | missense | DTX1 | GRCh38.p7 | 12:113094889 | TGGGCCGCCTGGGCC[A/G/T]CTGTGGCCACATGTA | 1840 |
rs368539864 | snp | C/G | 1.67438e-05 | 0.00289338 | intron-variant | DTX1 | GRCh38.p7 | 12:113095229 | CTTCCGCCTCTCTGG[C/G]CCCCAGCCCCCACAC | 1840 |
rs368804204 | in-del | -/G | 0.0225045 | 0.103662 | upstream-variant-2KB | DTX1 | GRCh38.p7 | 12:113055634 | CTGCAGGTCAGAGCA[-/G]GGGCCTGGGGAGGGG | 1840 |
rs368869708 | snp | C/T | 1.67891e-05 | 0.00289729 | missense | DTX1 | GRCh38.p7 | 12:113094849 | GAGGGCGTGCTTCGG[C/T]ACAAGGGCGTGCGGC | 1840 |
rs368900943 | snp | A/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113083844 | CTGGACCCAAACAGA[A/T]CCAGAGCCCTTTACA | 1840 |
rs369010505 | snp | A/G/T | 0.000336137 | 0.0129605 | intron-variant | DTX1 | GRCh38.p7 | 12:113094023 | CCTCAAACCCACCCC[A/G/T]CTGTGTCCCTGCAGG | 1840 |
rs369023989 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113078787 | GAGCAAGCATCAGCT[A/G]CTTGTCCAAAGTATT | 1840 |
rs369217142 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | DTX1 | GRCh38.p7 | 12:113058590 | TCCAGAAAAACAGGG[C/T]AGTCTAACCTTGTCC | 1840 |
rs369231642 | snp | A/G | 0.000153988 | 0.00877327 | intron-variant | DTX1 | GRCh38.p7 | 12:113094003 | CGGGGACAGACTCTG[A/G]GTACCCTCAAACCCA | 1840 |
rs369278026 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, utr-variant-5-prime | DTX1 | GRCh38.p7 | 12:113056762 | GGCCGCCAGCCGGCT[C/T]CTGCGTCCGTCCGTC | 1840 |
rs369314849 | in-del | -/AC | | | intron-variant | DTX1 | GRCh38.p7 | 12:113062032 | AATATTATATTTCAT[-/AC]ACACACACACACACA | 1840 |
rs369446455 | in-del | -/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113062360 | AATATGTAAGTGAAT[-/G]CGTGTGGCTGTGTTC | 1840 |
rs369544537 | snp | A/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113089796 | GACTGACTTTTGTAA[A/T]CTAGGGCTATGTGGT | 1840 |
rs369551827 | snp | C/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113089055 | CGGGAAGGTGTCTCA[C/G]ATAAGCTGACATTTG | 1840 |
rs369666602 | snp | C/T | 0.000199164 | 0.00997708 | intron-variant | DTX1 | GRCh38.p7 | 12:113095436 | GCCCAGCCGTGAGGG[C/T]ATGGGAGATAGGCAC | 1840 |
rs369731717 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DTX1 | GRCh38.p7 | 12:113092252 | CCGATGGCTGTGCTT[C/T]TAGTAGCTGTTAGGT | 1840 |
rs369823962 | snp | C/G | 0.000153988 | 0.00877327 | utr-variant-5-prime | DTX1 | GRCh38.p7 | 12:113058180 | GGACCTGGCCCCTGA[C/G]GCAGTGGCGGCCATG | 1840 |
rs369919406 | snp | G/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113076479 | AAAAAAAAAAAAAAG[G/T]GGGGCCGGTCATGGT | 1840 |
rs369971615 | snp | A/G | 8.26235e-05 | 0.00642689 | missense | DTX1 | GRCh38.p7 | 12:113095410 | ACAACGAGAAAGGCC[A/G]GAAGGTGGGTGCCCA | 1840 |
rs370019731 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113086461 | GGTCTGGAAGGTTGC[A/G]GTTAGGACTTTGGCT | 1840 |
rs370106874 | snp | C/T | 5.24095e-05 | 0.00511879 | missense | DTX1 | GRCh38.p7 | 12:113093650 | ACGTGAAGCCCGTGC[C/T]TGGCGTGCCCGGGGT | 1840 |
rs370198782 | in-del | -/TA | | | intron-variant | DTX1 | GRCh38.p7 | 12:113074240 | TCTCATATATATATA[-/TA]GTCAGTCAGGTAATG | 1840 |
rs370228021 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113069815 | AGTTGCTGGCACTGC[A/G]GAGCATTCGGTAAGG | 1840 |
rs370273142 | snp | A/G | 1.92114e-05 | 0.00309924 | intron-variant | DTX1 | GRCh38.p7 | 12:113077400 | GCCCGCTGTGCTGAC[A/G]CCTCCTCCCCATTTC | 1840 |
rs370359657 | snp | A/G/T | 0.000116498 | 0.00763128 | synonymous-codon | DTX1 | GRCh38.p7 | 12:113058315 | CTGGCGGCCCTACAC[A/G/T]GCCACCGTGTGCCAC | 1840 |
rs370396945 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | DTX1 | GRCh38.p7 | 12:113068646 | TGGGCTTCAGAGGCT[A/G]CTCTAAGGAGTTTAG | 1840 |
rs370402537 | snp | C/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113087828 | GGGTGGGAGGGGAGA[C/G]ATAAGGAGACCAGAC | 1840 |
rs370481380 | snp | A/G | 0.000164426 | 0.00906566 | missense, utr-variant-3-prime, nc-transcript-variant | DTX1, RASAL1 | GRCh38.p7 | 12:113096722 | CCCCCCAGGTGCTGC[A/G]GCTGCTCATCACGGC | 1840 |
rs370644778 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113059654 | CTAGAAATCCTTGGC[A/G]TGTTTGACCCCCCAA | 1840 |
rs370652803 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | DTX1 | GRCh38.p7 | 12:113075336 | TCACTCACTCCTCCC[A/C]CAAATACTGTGTGAG | 1840 |
rs370658900 | snp | A/G | | | intron-variant, downstream-variant-500B | DTX1, RASAL1 | GRCh38.p7 | 12:113096481 | AAAGAAAAAAAAGAA[A/G]AGGAAAGAAAAGAAA | 1840 |
rs370702255 | snp | C/T | | | missense, utr-variant-3-prime, nc-transcript-variant | DTX1, RASAL1 | GRCh38.p7 | 12:113096863 | CGGGCCACGGCTACC[C/T]GGACGCTAGCTACCT | 1840 |
rs370721847 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113090444 | AAAATCAAGACACCT[C/T]CACTCTCATCCCTGC | 1840 |
rs370777780 | snp | C/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113074443 | GGCTGGACAGTGCCT[C/G]GTGTATTTGAGGAAC | 1840 |
rs370804089 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | DTX1 | GRCh38.p7 | 12:113082731 | CTCCCAAGTAGGTGG[A/G]ACTACAGGCACGCAC | 1840 |
rs370829735 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | DTX1 | GRCh38.p7 | 12:113093314 | GCCCCCGAGATGGGC[C/T]GGTGAGCGTGGCCCG | 1840 |
rs370907894 | in-del | -/G | 0.0279526 | 0.114869 | intron-variant | DTX1 | GRCh38.p7 | 12:113079631 | CTCCAGGGTTCAAGT[-/G]ATTCTTCTGCCTCAG | 1840 |
rs370934901 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | DTX1 | GRCh38.p7 | 12:113095321 | GTACTGTCCCTCTCT[A/G]CAGGGCCCTGAGCAC | 1840 |
rs371042111 | in-del | -/TG | | | intron-variant | DTX1 | GRCh38.p7 | 12:113079694 | ACCATTCCCGGCTAC[-/TG]TGTGTGTGTGTGTGT | 1840 |
rs371120123 | snp | G/T | 0.000618559 | 0.0175755 | intron-variant | DTX1 | GRCh38.p7 | 12:113094741 | AGTGCTGACCCAGTA[G/T]GTGCCCTGCCCTCCC | 1840 |
rs371131840 | snp | C/G | | | upstream-variant-2KB | DTX1 | GRCh38.p7 | 12:113054894 | GTAAAATGAGGACAA[C/G]ATTACCTTCCTTGTG | 1840 |
rs371174853 | snp | C/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113087917 | GGATCCTGGACCCCT[C/G]TAGGGGACAGAGAGA | 1840 |
rs371376467 | snp | C/G | 5.06924e-05 | 0.00503424 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant | DTX1, RASAL1 | GRCh38.p7 | 12:113096774 | CACTATCGGCACGTC[C/G]AACACCACGGGCGAG | 1840 |
rs371426051 | snp | C/G/T | 0.000881414 | 0.0209745 | intron-variant | DTX1 | GRCh38.p7 | 12:113093509 | GCGGGGATGGCGCCC[C/G/T]GCCCTGTGACTGCGC | 1840 |
rs371460381 | in-del | -/TATT | 0.00874735 | 0.0655527 | intron-variant | DTX1 | GRCh38.p7 | 12:113066671 | TGTGATTGTGGTCAC[-/TATT]CATTCATTCATCAGG | 1840 |
rs371471557 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113071613 | CTTCTTAGACCCATT[A/G]TTCTGGCTGAAAATC | 1840 |
rs371603647 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113075989 | ACAGAAACCAAGATA[A/G]ATGGGTAGAATGTGA | 1840 |
rs371714740 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113080000 | ACAGCATCTACACTG[A/G]CAGTAGTTCAGCCAT | 1840 |
rs371842344 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113091137 | GCAGTAGCAGGTGCG[A/G]TACTGGTCTACATGA | 1840 |
rs372006093 | snp | C/T | | | intron-variant, downstream-variant-500B | DTX1, RASAL1 | GRCh38.p7 | 12:113096345 | TTGGAGAGGCTGATG[C/T]GGGACGATTGTTGGA | 1840 |
rs372008981 | snp | C/G | 0.00119737 | 0.0244387 | upstream-variant-2KB | DTX1 | GRCh38.p7 | 12:113055790 | CAGGCGCCCAAACAG[C/G]CCACTGACCCCCGTC | 1840 |
rs372131565 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DTX1 | GRCh38.p7 | 12:113088907 | GTAGTCCCAGCTACT[C/T]AAGAGGCTGAGGTGG | 1840 |
rs372156276 | in-del | -/AAAAA | | | intron-variant, downstream-variant-500B | DTX1, RASAL1 | GRCh38.p7 | 12:113096504 | AAAGAAAAGAAAAAA[-/AAAAA]CAAACATAAGTAACT | 1840 |
rs372239296 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | DTX1 | GRCh38.p7 | 12:113061527 | CCTCTCCAGGTCTCA[G/T]TTTCCACATCCGTGA | 1840 |
rs372241867 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113091530 | TGTGTAATGTGTCCC[A/G]GGGAGTATGATAAGT | 1840 |
rs372433038 | snp | C/T | 1.68241e-05 | 0.00290031 | synonymous-codon | DTX1 | GRCh38.p7 | 12:113094857 | GCTTCGGCACAAGGG[C/T]GTGCGGCCTGAGCTC | 1840 |
rs372532859 | snp | C/G/T | 0.000965082 | 0.0219459 | synonymous-codon | DTX1 | GRCh38.p7 | 12:113077584 | GCAGCACCCGTGGCT[C/G/T]GACCTCTCATCGCTA | 1840 |
rs372559593 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | DTX1 | GRCh38.p7 | 12:113070105 | TGCTCCTAACTGCTC[C/T]GTGCCTCTGTTTTCT | 1840 |
rs372564180 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | DTX1 | GRCh38.p7 | 12:113087728 | GGGGTCTGCTGGGTA[A/C]GTGTGAGGTATCCTG | 1840 |
rs372573770 | snp | A/G | 0.000142304 | 0.00843396 | intron-variant | DTX1 | GRCh38.p7 | 12:113077375 | CGCCCTTCCAGCCGC[A/G]CAGACCAACGCCCGC | 1840 |
rs372614906 | in-del | -/GGA | | | intron-variant | DTX1 | GRCh38.p7 | 12:113065830 | CAAGGGGTTGGGGCA[-/GGA]CTGGTCACAGTGGCT | 1840 |
rs372616653 | in-del | -/AG | | | intron-variant | DTX1 | GRCh38.p7 | 12:113093045 | TGCAGTTGRSAGAGA[-/AG]GGTACAAAGAGGCCA | 1840 |
rs372662785 | snp | A/G | 0.000153988 | 0.00877327 | missense | DTX1 | GRCh38.p7 | 12:113094079 | AGATACATGCAGAAG[A/G]TGAAAAACCCACCTG | 1840 |
rs372733552 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | DTX1 | GRCh38.p7 | 12:113080896 | AAGAGGATCACTTGA[A/G]CCCAGTAGGTCAAGG | 1840 |
rs372810439 | snp | A/C/T | 4.95776e-05 | 0.00497863 | missense, synonymous-codon | DTX1 | GRCh38.p7 | 12:113095137 | CCACCTCATCCCCCA[A/C/T]TCGCTGCCCGGCTTC | 1840 |
rs372819689 | snp | C/T | 9.97208e-05 | 0.00706048 | synonymous-codon | DTX1 | GRCh38.p7 | 12:113058390 | CCTGGGGCAGGTGGA[C/T]GCCCAGCTTGTGCCC | 1840 |
rs372821568 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113086018 | CACACCTGTAATCCC[A/G]GCACTTTGGGAGGCT | 1840 |
rs372986332 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113084685 | CCACTGTGTCTGGCC[A/G]TTTACAGGCATGTCT | 1840 |
rs373115107 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DTX1 | GRCh38.p7 | 12:113062936 | GTCTGGACTGGAAAC[C/T]GGAGCCCCTCCACGG | 1840 |
rs373373810 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | DTX1 | GRCh38.p7 | 12:113082156 | CCCTGAGCCCAGACA[C/T]TGGCCTGGAAAACAG | 1840 |
rs373457698 | snp | C/G | 1.92395e-05 | 0.00310151 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant | DTX1, RASAL1 | GRCh38.p7 | 12:113096729 | GGTGCTGCGGCTGCT[C/G]ATCACGGCCTGGGAG | 1840 |
rs373543134 | snp | A/T | 1.66532e-05 | 0.00288554 | intron-variant | DTX1 | GRCh38.p7 | 12:113095446 | GAGGGCATGGGAGAT[A/T]GGCACAGGCAGGGGC | 1840 |
rs373551570 | in-del | -/AAA | | | intron-variant | DTX1 | GRCh38.p7 | 12:113080987 | CTCAAAAAAAAAAAA[-/AAA]TTGCTCCATGAATGT | 1840 |
rs373556695 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113087145 | AGTGACCCCCGCAGC[C/T]CCCATACCTCTAGAT | 1840 |
rs373611766 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113092405 | GATGTGCTGTGTGTC[A/G]CCCAGCTCATTAGTG | 1840 |
rs373646477 | in-del | -/A | | | intron-variant | DTX1 | GRCh38.p7 | 12:113086700 | TATGCTTTTATTTTT[-/A]AAAAAATCCACATTT | 1840 |
rs373666948 | snp | G/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113085746 | CAGGCACTGTTTGGG[G/T]CCCTGGGGACACAGC | 1840 |
rs373784076 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | DTX1 | GRCh38.p7 | 12:113086316 | CCAACATGCCAGACA[G/T]CAGAACAGCATGTGC | 1840 |
rs373819348 | in-del | -/ATTT | 0.0023933 | 0.0345097 | intron-variant | DTX1 | GRCh38.p7 | 12:113094266 | GTTTAATAGACTCAC[-/ATTT]ATCCATCTTTTGATG | 1840 |
rs373827220 | snp | C/T | 0.000153988 | 0.00877328 | missense | DTX1 | GRCh38.p7 | 12:113058208 | ATGTCACGGCCAGGC[C/T]ACGGTGGGCTGATGC | 1840 |
rs373923340 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113061321 | CGATTGGCAGGAGAC[C/T]TCAGCTGCCTGGGAA | 1840 |
rs373925500 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113087792 | TAGCATCAGAGAAAG[C/T]AACAAGTCTAGGCCT | 1840 |
rs374220260 | snp | C/G | 5.90941e-05 | 0.0054354 | intron-variant | DTX1 | GRCh38.p7 | 12:113094751 | CAGTAGGTGCCCTGC[C/G]CTCCCCAGTCCTCAG | 1840 |
rs374290777 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113075564 | CTGCGGCCTGGACCT[G/T]GGGTTATCTCTGGTT | 1840 |
rs374361452 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113063766 | GCCCTGGTCCCTGCC[A/G]TGAGAGGAAGCACTA | 1840 |
rs374367644 | snp | C/T | 1.6599e-05 | 0.00288084 | synonymous-codon | DTX1 | GRCh38.p7 | 12:113058357 | CGTGCTGAAGGAGGA[C/T]GCTCGCGGTTCCGTG | 1840 |
rs374373983 | snp | C/T | 3.36598e-05 | 0.00410229 | intron-variant | DTX1 | GRCh38.p7 | 12:113093522 | CCCGCCCTGTGACTG[C/T]GCCCCCTAACCCCCA | 1840 |
rs374382565 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | DTX1 | GRCh38.p7 | 12:113070269 | TTCTGGGTTGGTGAA[A/G]GATTCAGTGAAGTCT | 1840 |
rs374508942 | snp | A/G | 3.36479e-05 | 0.00410157 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant | DTX1, RASAL1 | GRCh38.p7 | 12:113096783 | CACGTCCAACACCAC[A/G]GGCGAGTCGGACACC | 1840 |
rs374516614 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | DTX1 | GRCh38.p7 | 12:113071161 | TGACAGTCTCTTTGA[C/T]CATGTATGTCTCTCT | 1840 |
rs374520409 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113059202 | ATGGATGATGGTGAC[A/G]TGGCAGTGTTGGTGG | 1840 |
rs374650291 | snp | G/T | | | utr-variant-5-prime | DTX1 | GRCh38.p7 | 12:113058075 | CCCAGAGTTAGAAAG[G/T]AGGCCAGACGGTCCT | 1840 |
rs374679797 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113061471 | GAAAAGAGCCTCAAC[C/T]GGCAGGGAGCAGACC | 1840 |
rs374740078 | snp | A/G | 9.88533e-05 | 0.00702971 | missense | DTX1 | GRCh38.p7 | 12:113095346 | GAGCACCCCAACCCC[A/G]GGAAGAAGTTCACCG | 1840 |
rs374742094 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113095744 | CCACCACCCTACAGG[C/T]TGTCTGATTTGACTT | 1840 |
rs374757550 | snp | A/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113073086 | CCTGCCGAGCTCAGG[A/T]TTTGGCACACAGGGG | 1840 |
rs374845117 | snp | G/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113073536 | GGGCGGGGTTGAAGA[G/T]GTGGAGAGGTTGGAC | 1840 |
rs374856244 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113087048 | CTCCCCTACCTGACC[A/G]GTCCTCCCTGCCCCC | 1840 |
rs374935355 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113071060 | TTCCAGCTTCCCTTT[C/T]TTTTCATCTCTCAAG | 1840 |
rs374968790 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | DTX1 | GRCh38.p7 | 12:113082553 | CTCTCGTCCCCAAAC[C/T]ACCTCCCAGCCCTCC | 1840 |
rs375008930 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | DTX1 | GRCh38.p7 | 12:113069833 | GCATTCGGTAAGGTG[C/T]TGGGTGCCGCTGTTG | 1840 |
rs375020755 | snp | C/T | 8.43092e-05 | 0.00649211 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant | DTX1, RASAL1 | GRCh38.p7 | 12:113096885 | TAGCTACCTAGACAA[C/T]GTGCTGGCTGAGCTC | 1840 |
rs375367925 | snp | A/G | | | intron-variant, downstream-variant-500B | DTX1, RASAL1 | GRCh38.p7 | 12:113096469 | AAAAAAAAAGAAAAA[A/G]AAAAAAAAGAAAAGG | 1840 |
rs375462327 | in-del | -/AG | | | intron-variant | DTX1 | GRCh38.p7 | 12:113093041 | TAACTGCAGTTGGCA[-/AG]GAGAGGTACAAAGAG | 1840 |
rs375471619 | snp | C/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113075201 | GAGAAAACTGGGGCC[C/G]AGAGATGCTGAGTTG | 1840 |
rs375478293 | snp | C/T | | | upstream-variant-2KB | DTX1 | GRCh38.p7 | 12:113056336 | CTGAATCAGGCCTTG[C/T]CAGCACCCTCCCACC | 1840 |
rs375728435 | in-del | -/G | | | intron-variant, downstream-variant-500B | DTX1, RASAL1 | GRCh38.p7 | 12:113096463 | AAAAAAAAAAAAAAA[-/G]AAAAAGAAAAAAAAG | 1840 |
rs375875690 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113063308 | GCTCCCAGAGAAGAA[A/G]CCACATCTTCCCTGG | 1840 |
rs375934553 | snp | A/C/G | 5.03667e-05 | 0.00501809 | missense | DTX1 | GRCh38.p7 | 12:113094847 | ACGAGGGCGTGCTTC[A/C/G]GCACAAGGGCGTGCG | 1840 |
rs375936872 | snp | G/T | 0.000339018 | 0.0130151 | utr-variant-5-prime | DTX1 | GRCh38.p7 | 12:113058154 | GGAGGAGCTGGGCCT[G/T]CAATAGTGGGGGACC | 1840 |
rs376025049 | snp | A/C | | | intron-variant | DTX1 | GRCh38.p7 | 12:113081846 | ACCACCGGGGGATAG[A/C]GGCTCCCTTCTGGAA | 1840 |
rs376084266 | snp | A/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113069777 | GTGAGGACTGGGAGA[A/T]GATGTGTGTGAGCCC | 1840 |
rs376216602 | snp | C/T | 0.000377515 | 0.0137337 | intron-variant | DTX1 | GRCh38.p7 | 12:113093138 | GCTGGAGTCCAGCTG[C/T]GGCCTCTTCTCTTCT | 1840 |
rs376244804 | snp | C/T | 0.000153988 | 0.00877328 | synonymous-codon | DTX1 | GRCh38.p7 | 12:113058417 | GCCCTACATCATCGA[C/T]CTGCAGTCCATGCAC | 1840 |
rs376334040 | snp | C/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113063032 | AGGGTTGGAGGGAGA[C/G]TCAGAGCTGGGCGAG | 1840 |
rs376370338 | snp | C/T | 8.3575e-05 | 0.00646379 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant | DTX1, RASAL1 | GRCh38.p7 | 12:113096855 | CAACCTCACGGGCCA[C/T]GGCTACCCGGACGCT | 1840 |
rs376402916 | in-del | -/AG | 0.00318978 | 0.0398085 | intron-variant | DTX1 | GRCh38.p7 | 12:113080270 | CCAAAGCTGCAGGAT[-/AG]AGTCACTGAGATCTC | 1840 |
rs376460047 | snp | C/G | 1.68397e-05 | 0.00290165 | missense | DTX1 | GRCh38.p7 | 12:113094869 | GGGCGTGCGGCCTGA[C/G]CTCGTGGGCCGCCTG | 1840 |
rs376509613 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113069417 | GCCCTTCAGCCTTCC[C/T]TAGGCAGCACTGCAG | 1840 |
rs376513538 | snp | C/G | 0.00636936 | 0.0560724 | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | RASAL1, DTX1 | GRCh38.p7 | 12:113098332 | GGAAATACGGAGGAG[C/G]TGGGAGACACTGTGA | 1840 |
rs376519490 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113082516 | CTTTGAGGAGCCAGG[C/T]AGACAGGTCTACCCA | 1840 |
rs376538262 | snp | A/G | 1.67508e-05 | 0.00289398 | intron-variant | DTX1 | GRCh38.p7 | 12:113095458 | GATAGGCACAGGCAG[A/G]GGCTCCAGCAACCAC | 1840 |
rs376558485 | snp | C/T | 0.000269778 | 0.011611 | intron-variant | DTX1 | GRCh38.p7 | 12:113094022 | CCCTCAAACCCACCC[C/T]GCTGTGTCCCTGCAG | 1840 |
rs376567903 | snp | C/T | 0.000116001 | 0.00761491 | intron-variant | DTX1 | GRCh38.p7 | 12:113095428 | AGGTGGGTGCCCAGC[C/T]GTGAGGGCATGGGAG | 1840 |
rs376713779 | snp | A/T | 0.000153988 | 0.00877328 | stop-lost, utr-variant-3-prime, nc-transcript-variant | DTX1, RASAL1 | GRCh38.p7 | 12:113096937 | GCTGCAGCCAAGGCT[A/T]GAGGCCCAAGGCTGC | 1840 |
rs376728200 | snp | C/T | 0.000388825 | 0.0139378 | intron-variant | DTX1 | GRCh38.p7 | 12:113094988 | GGAGTGGGCAGGGAA[C/T]GGAGTGGGGTTTGGG | 1840 |
rs376780413 | in-del | -/C | | | intron-variant | DTX1 | GRCh38.p7 | 12:113072696 | GACCTGAGAGATTTT[-/C]TTTTTTTTTTTTTTT | 1840 |
rs376795333 | snp | C/T | | | upstream-variant-2KB, intron-variant | DTX1 | GRCh38.p7 | 12:113057352 | GCTGTCCCCCTTCGG[C/T]TCCCCATTGTTCTCA | 1840 |
rs376848719 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | DTX1 | GRCh38.p7 | 12:113081216 | AGCATGGTGGTACAC[A/G]CCTGTAATCCCAGCT | 1840 |
rs376860999 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113091787 | GCCAAGGGGGCTGCT[A/G]CAGCTCCTTCTCCAG | 1840 |
rs376989727 | snp | C/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113075256 | AAGTCAGAAAGTCAG[C/G]ACTTGAAGTGAGGGC | 1840 |
rs377098347 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113061927 | GCCAAGCTGGTCTTG[A/G]ACTCCTGGCCTCAAG | 1840 |
rs377132635 | snp | C/T | 9.91539e-05 | 0.00704039 | missense | DTX1 | GRCh38.p7 | 12:113095138 | CACCTCATCCCCCAC[C/T]CGCTGCCCGGCTTCC | 1840 |
rs377140287 | snp | C/T | 3.50889e-05 | 0.00418847 | intron-variant | DTX1 | GRCh38.p7 | 12:113093725 | CCACGCCCTGCCTCA[C/T]ACGAGATGAACCCCA | 1840 |
rs377153937 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | DTX1 | GRCh38.p7 | 12:113089582 | CTCGGAGGAAACAGC[A/G]TGTCCCACATCAAAA | 1840 |
rs377223673 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113062535 | TTTGGCCTGTGTGCT[A/G]CAGGTTCACTGACCC | 1840 |
rs377259444 | snp | C/T | 0.000153988 | 0.00877328 | synonymous-codon | DTX1 | GRCh38.p7 | 12:113058210 | GTCACGGCCAGGCCA[C/T]GGTGGGCTGATGCCT | 1840 |
rs377314385 | in-del | -/AA | 0.443195 | 0.158668 | intron-variant | DTX1 | GRCh38.p7 | 12:113076459 | CAATACTCTGCCTGG[-/AA]AAAAAAAAAAAAAAA | 1840 |
rs377325234 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113070270 | TCTGGGTTGGTGAAG[C/G]ATTCAGTGAAGTCTC | 1840 |
rs377381641 | snp | C/T | 5.09481e-05 | 0.00504692 | missense, utr-variant-3-prime, nc-transcript-variant | DTX1, RASAL1 | GRCh38.p7 | 12:113096770 | TCTTCACTATCGGCA[C/T]GTCCAACACCACGGG | 1840 |
rs377553830 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113059397 | CTGTGTGTGGCTGTT[A/G]CTTAGTGGTATTGGT | 1840 |
rs377595247 | snp | A/C | | | intron-variant | DTX1 | GRCh38.p7 | 12:113070565 | AACCCTCCCCCTTCT[A/C]CATGGAGTCAGCTGC | 1840 |
rs386766431 | multinucleotide-polymorphism | CT/TG | | | intron-variant | DTX1 | GRCh38.p7 | 12:113059004 | ACTGGTATCCTATAC[CT/TG]GCTCCAAGTGTTGGT | 1840 |
rs386766432 | in-del | AA/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113067889 | AAAAACAAAAAAAAA[AA/T]TAGCTAGACATGATG | 1840 |
rs386766433 | multinucleotide-polymorphism | GA/TG | | | intron-variant | DTX1 | GRCh38.p7 | 12:113074068 | AAATCCCGTCTCTAC[GA/TG]AAAATACAAAAAAAA | 1840 |
rs386766434 | multinucleotide-polymorphism | CAA/TAC | | | intron-variant | DTX1 | GRCh38.p7 | 12:113077108 | TGGCTCTCCCGCCCC[CAA/TAC]GCCCAATCTACTGAC | 1840 |
rs397775312 | in-del | -/AG | | | intron-variant | DTX1 | GRCh38.p7 | 12:113093046 | GCAGTTGGCAGAGAG[-/AG]GTACAAAGAGGCCAG | 1840 |
rs397824528 | in-del | -/A | | | intron-variant | DTX1 | GRCh38.p7 | 12:113092339 | TTAAAAAAAAAAAAA[-/A]GGTACCATATTGTCC | 1840 |
rs398021102 | in-del | -/A | 0 | 0 | intron-variant | DTX1 | GRCh38.p7 | 12:113067890 | AAAACAAAAAAAAAA[-/A]TAGCTAGACATGATG | 1840 |
rs398044815 | in-del | -/A | 0.5 | 0 | intron-variant, downstream-variant-500B | DTX1, RASAL1 | GRCh38.p7 | 12:113096458 | AAAAAAAAAAAAAAA[-/A]AGAAAAAGAAAAAAA | 1840 |
rs398070186 | in-del | -/AA | | | intron-variant | DTX1 | GRCh38.p7 | 12:113087128 | ACCGGGAGGGTTGAA[-/AA]GAGTGACCCCCGCAG | 1840 |
rs527279831 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | DTX1 | GRCh38.p7 | 12:113093287 | CAGCTCCGCCTGTCA[C/G]CCGGTGACCCCGCCC | 1840 |
rs527280654 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DTX1 | GRCh38.p7 | 12:113086584 | GACCGCAGTGGGGCT[A/G]AAGCAGGAGGCCAAG | 1840 |
rs527289298 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | DTX1 | GRCh38.p7 | 12:113055213 | AGAGACACGAGTTCT[C/T]CTTTCCAATTTGCTG | 1840 |
rs527309513 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DTX1 | GRCh38.p7 | 12:113092797 | GCTACATCTAACAAG[C/T]TTTGAGAGATGTTAA | 1840 |
rs527368630 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | DTX1 | GRCh38.p7 | 12:113054808 | ACCCTAGCTCTGCCA[C/T]TTACTCCTTGTGGGA | 1840 |
rs527483421 | in-del | -/CT | 0.121717 | 0.214577 | intron-variant | DTX1 | GRCh38.p7 | 12:113087143 | GAGTGACCCCCGCAG[-/CT]CCCCCATACCTCTAG | 1840 |
rs527546976 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113080077 | GGGCGGGGAAGCTGT[A/G]ATTTTCCAGGGATGC | 1840 |
rs527736010 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113068279 | GTGACTGTAAACCAG[C/T]CCAGCCTTGGAGGGG | 1840 |
rs527824838 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113074666 | GGATCCCTCTGGCTG[C/T]GGTATGGGAAATGGA | 1840 |
rs527895143 | snp | C/T | | | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | DTX1, RASAL1 | GRCh38.p7 | 12:113098313 | CAGAGCTGGGAGCCT[C/T]GAGGGAAATACGGAG | 1840 |
rs527905525 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113094503 | GGATCTCTTGAGCCC[A/G]GGAGTTTGACTCTGC | 1840 |
rs527980207 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | DTX1 | GRCh38.p7 | 12:113056526 | TCAAGCCGGTGACTC[C/T]TAAACATCCCACTCC | 1840 |
rs528064690 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113067672 | CCAAGGAGGCCAATT[A/G]TTGTGGCCCCACCCT | 1840 |
rs528083188 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113062384 | TGTGTTCTAATCAAA[C/T]TAGTTGTGGACACAG | 1840 |
rs528142857 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113070707 | AAGTAAAGCTGAAGT[A/G]GTGAGCTCTCCATCG | 1840 |
rs528144155 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113063850 | AGCTTTTCCCATCAC[C/G]GGGGAAAACACCTCC | 1840 |
rs528216457 | snp | A/G/T | 0.000555739 | 0.0166615 | intron-variant | DTX1 | GRCh38.p7 | 12:113094140 | GGAGGGCCCTGGCAT[A/G/T]GAGGGGGCAGGAACC | 1840 |
rs528237092 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113070257 | TAGTATTATGACTTC[C/T]GGGTTGGTGAAGGAT | 1840 |
rs528321574 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113090512 | CTTTCACAGGACTCT[A/G]TCCCCATTACAGGTG | 1840 |
rs528322859 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | DTX1, RASAL1 | GRCh38.p7 | 12:113097247 | TGCACGCACACCCAC[A/G]TGCCTGTACTTGCCC | 1840 |
rs528365841 | in-del | -/GGAG | 0.00159617 | 0.0282053 | upstream-variant-2KB, utr-variant-5-prime | DTX1 | GRCh38.p7 | 12:113057681 | AAGGGGGCCCAGACC[-/GGAG]GGAGGGAGGCGAGAA | 1840 |
rs528422058 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-5-prime | DTX1 | GRCh38.p7 | 12:113057934 | CTGTTTCCTCCGGCA[C/T]AAGAGAGACACTTGC | 1840 |
rs528442510 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | DTX1 | GRCh38.p7 | 12:113065158 | CAGCCACGCTGCAGG[A/C]CCAGCCTCATTAATC | 1840 |
rs528562889 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DTX1 | GRCh38.p7 | 12:113085379 | TTTAAATCCACCCTT[A/G]TCCCTCCCATCTCTA | 1840 |
rs528600869 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113084547 | TGCACCACCATGCCC[A/G]GCCAATTTTTTATTT | 1840 |
rs528674219 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | DTX1 | GRCh38.p7 | 12:113059234 | GATGTCAGTGATAGC[A/G]TTAACCATGGGATTC | 1840 |
rs528675105 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113060465 | GATGTTTGAACAGAG[A/G]TCTGAAGAATGAGTG | 1840 |
rs528676296 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113066672 | GTGATTGTGGTCACT[A/G]TTCATTCATTCATCA | 1840 |
rs528711250 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113066231 | CAGCTGCTTACTAAG[A/G]ATCATGGGGTGTGTA | 1840 |
rs528735047 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113073008 | CACTGCACCTGGCTC[A/G]ACCCGAGAGACTTCT | 1840 |
rs528823962 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113072081 | CCCCAGGGACCCCTC[A/G]AAGCTTGGCCTCCAC | 1840 |
rs528900257 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113065575 | TCCCATCCCCCGCCT[C/T]ATTCTTCCAAAGGAG | 1840 |
rs528964122 | snp | C/G/T | 0.00119737 | 0.0244387 | intron-variant | DTX1 | GRCh38.p7 | 12:113067234 | ACTGCAAGCAGAGCA[C/G/T]GGTAAGAGGAAGCAC | 1840 |
rs529021392 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113064587 | GGACAACAGATACAG[A/T]CCTAAAACCCAGCTT | 1840 |
rs529122601 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113091828 | TCCCAGCCCTTCCTG[C/T]CCCCTCTCCTGGCAC | 1840 |
rs529164102 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | DTX1, RASAL1 | GRCh38.p7 | 12:113097734 | TTTTGAGAGCCAAAG[C/G]CTGGCGCTTCTGACT | 1840 |
rs529216057 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113087047 | CCTCCCCTACCTGAC[C/T]GGTCCTCCCTGCCCC | 1840 |
rs529255199 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | DTX1 | GRCh38.p7 | 12:113095912 | CTTTCTTCACCCCAG[-/A]AAAAAACAGGCAGGG | 1840 |
rs529290188 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113073133 | GTTCCCATTGCTTCC[C/T]TTCCTATCCTGCACA | 1840 |
rs529379274 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | DTX1 | GRCh38.p7 | 12:113079374 | CCTTTGGGGTCACTG[C/T]ATCCAGCTCACCCCT | 1840 |
rs529438572 | snp | A/C | | | intron-variant | DTX1 | GRCh38.p7 | 12:113082161 | AGCCCAGACATTGGC[A/C]TGGAAAACAGAAGAT | 1840 |
rs529515960 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113067487 | CTACACAAAGGCTGC[A/C]AATTCAGATGCTTAC | 1840 |
rs529545336 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113059902 | CTCATAGCCACATGT[A/G]TCTTGTGGTACCTTG | 1840 |
rs529634085 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113075883 | CAAATATCGCTCGAG[C/T]ACCTGCTGTGTGCAG | 1840 |
rs529841961 | in-del | -/G | 0.00159617 | 0.0282053 | intron-variant | DTX1 | GRCh38.p7 | 12:113070518 | CCGTTTAGAGGCTGA[-/G]GGACCAGCAGGAGGA | 1840 |
rs529855028 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | DTX1 | GRCh38.p7 | 12:113057048 | GCTGTTACCCCCAGG[A/G]CGGGAGGCAGAGACG | 1840 |
rs529895017 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113063080 | GCTTCGCAGTACTGA[A/G]CCAAGTGCCCGGTTT | 1840 |
rs529912570 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113089044 | AATAAAGTGGTCGGG[A/G]AGGTGTCTCAGATAA | 1840 |
rs529918146 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113063607 | GATGCCAGCTGGGGA[C/T]CATCCAAAGATGCCA | 1840 |
rs529987007 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | DTX1 | GRCh38.p7 | 12:113069664 | GAATCCCAGCCCAGC[C/T]GGTGCCCCCAGCCAG | 1840 |
rs530163556 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, utr-variant-5-prime | DTX1 | GRCh38.p7 | 12:113057475 | GAGTGGGGTGGGGCG[C/T]GCCCACGGGCCCCCG | 1840 |
rs530209090 | snp | C/T | 0.00956916 | 0.0685055 | missense | DTX1 | GRCh38.p7 | 12:113077865 | CGCCCCCGCTGCCGC[C/T]GCCGCCGCCACCTGG | 1840 |
rs530210056 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DTX1 | GRCh38.p7 | 12:113070805 | CCTGCCTTTACTCCA[C/T]GAGTGTGGCATCATT | 1840 |
rs530251859 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | DTX1 | GRCh38.p7 | 12:113065261 | TTCACCCAGCCAGCG[A/G]GTGTCACCCCATTTT | 1840 |
rs530504985 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113070229 | AGTGTGCTCTCTGAG[C/T]GTGGATGGCTGTTAG | 1840 |
rs530595158 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | DTX1 | GRCh38.p7 | 12:113076357 | CCAGCTACTCAGGAG[G/T]CTGAGGCAGGAGAAT | 1840 |
rs530626198 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113068117 | GAACAAAACCATATC[C/T]GCCCAGCTTGCAGTC | 1840 |
rs530634991 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113075922 | GATATAGCAGTAAAT[A/C/G]AAACAAAATCCCTGA | 1840 |
rs530669404 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | DTX1 | GRCh38.p7 | 12:113062654 | TGTACCAAGGTACAC[A/G]TGCGTGTGCGTACAC | 1840 |
rs530754841 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime | DTX1 | GRCh38.p7 | 12:113057919 | CCAAGGACTTTAGAG[C/T]TGTTTCCTCCGGCAT | 1840 |
rs530758286 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113063673 | CCCAAGCTGGCCAAC[A/G]GGCTGGAGTGGCAGG | 1840 |
rs530806144 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DTX1 | GRCh38.p7 | 12:113077243 | TGAACCTCATGCCTG[A/G]GCCTTGACCTCCTTC | 1840 |
rs530996358 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113072032 | AGCTGGCCAACGCTG[A/T]TGTTGAGAATCCTCC | 1840 |
rs530996437 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DTX1 | GRCh38.p7 | 12:113065336 | GACGCTGAGAAGAGA[C/T]GGGTCTGAGATCAGA | 1840 |
rs531048376 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113090423 | CCCCGCAGGGTGCCC[A/G]ACAAGAAAATCAAGA | 1840 |
rs531133949 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113062192 | CTGAACTTGAACTTT[A/G]AGGGGAGACTGCCCT | 1840 |
rs531207256 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113080221 | AGAGAGCAGACTTGA[A/G]GGGGTCAAAGAAGAC | 1840 |
rs531334401 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | DTX1 | GRCh38.p7 | 12:113055432 | TTGCCTGTAATGGGA[A/G]AGGGGGACTTCATGG | 1840 |
rs531457458 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113093332 | TGAGCGTGGCCCGGA[A/G]GAAACGCCCCCTTCC | 1840 |
rs531513687 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113080946 | CACCACTGCACTGCA[G/T]CCTGAGAGACAGAGC | 1840 |
rs531516622 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113068556 | TACAGAGGCATAACC[A/G]CACACACGGTATGTT | 1840 |
rs531757779 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113069128 | CATAGTAGGCCCTCT[G/T]GGAGTGTTTATTATC | 1840 |
rs531759082 | snp | G/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | DTX1 | GRCh38.p7 | 12:113056571 | GCTTGGGGTCAGAAG[G/T]CCCCTTGGGGTCTCG | 1840 |
rs531810854 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DTX1 | GRCh38.p7 | 12:113082188 | AGATGTGGGGTGGGG[A/G]AAACTTCTCAAGAAC | 1840 |
rs531812291 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113079039 | TGGGCACCCAGCTTG[C/T]ATCAAGTTTGCAAAT | 1840 |
rs531845318 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113089314 | TGAGCAAAGTGGGAG[C/T]TGCAGGAGGAGTGAG | 1840 |
rs531918448 | snp | A/G | | | intron-variant, downstream-variant-500B | DTX1, RASAL1 | GRCh38.p7 | 12:113096044 | AACCCCGTCTCTACT[A/G]AAAATACAAAAATTA | 1840 |
rs531943405 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113095691 | AGAGAAACTAAGTGG[C/T]GGAGCTGGGATTTGA | 1840 |
rs532008013 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | DTX1 | GRCh38.p7 | 12:113081382 | GTTCTAGAGGAGGCT[A/G]AAAATTACTCAGCTT | 1840 |
rs532051793 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | DTX1 | GRCh38.p7 | 12:113088531 | AGTTAATGGGCGCAG[C/G]ACACCAGCATGGCAC | 1840 |
rs532063887 | snp | C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, utr-variant-5-prime | DTX1 | GRCh38.p7 | 12:113056908 | GCGGCGGTGCTGGAG[C/G]GCGAGCCGGAGCCGG | 1840 |
rs532160654 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113062536 | TTGGCCTGTGTGCTG[C/T]AGGTTCACTGACCCC | 1840 |
rs532177663 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113088394 | TAGTGGTATGCACTC[A/G]TATATTTGACATTCC | 1840 |
rs532314632 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113075185 | TGCCCATTTTCAACA[A/T]GAGAAAACTGGGGCC | 1840 |
rs532363483 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113089503 | TAGGGGTGAAGGCTG[G/T]CTCCCCTTCCGGGAG | 1840 |
rs532455042 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | DTX1 | GRCh38.p7 | 12:113092038 | GTCCTCCCAACGACT[A/G]TAAGTGAGGTGTTAA | 1840 |
rs532462967 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | DTX1 | GRCh38.p7 | 12:113056979 | GGGACCCCACCCCCG[A/G]CTCCCGCTGGGGGCC | 1840 |
rs532516292 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113063056 | GGGCGAGGGATGGGT[C/T]GCTTGCTCGCTTCGC | 1840 |
rs532529997 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | DTX1 | GRCh38.p7 | 12:113067004 | CCCTCTGGAGCTGCT[C/T]CAGGCTGCTACTGCT | 1840 |
rs532533831 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113095989 | AAGGCGGGCAGATCA[C/T]GAGATCAGGAGTTTG | 1840 |
rs532561498 | snp | C/T | 0.00755907 | 0.0610114 | upstream-variant-2KB, intron-variant | DTX1 | GRCh38.p7 | 12:113057411 | GGGGTGCTGCGCTCT[C/T]CTCTTAAAGGGCCCT | 1840 |
rs532562329 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DTX1 | GRCh38.p7 | 12:113095472 | GGGGCTCCAGCAACC[A/G]CTGGCCTGGGCCTGT | 1840 |
rs532576700 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113076390 | CTTGAACCTGGAGGC[A/G]GAGATTGCATTGAGC | 1840 |
rs532601285 | snp | A/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113086177 | GGAGGCTGAGGTGGG[A/T]GGATCCCTTGAGCCC | 1840 |
rs532635649 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113082653 | CAGGCTGGAGTACAG[C/T]GGCGCAATCACAGCT | 1840 |
rs532671981 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113089865 | TAAATCCTTCCCTTC[C/G]TGGAGTACCCTCTGT | 1840 |