SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs8907 | snp | A/G | 0.183946 | 0.241116 | synonymous-codon, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51260914 | GTTGCTGCGGCGTCT[A/G]CGAGGCCCGAGGGTG | 51096 |
rs14180 | snp | C/T | 0.236407 | 0.24963 | synonymous-codon, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51260896 | CGAGAACGACGAGGA[C/T]GCGTTGCTGCGGCGT | 51096 |
rs917654 | snp | C/G | 0.437401 | 0.165472 | intron-variant | UTP18 | GRCh38.p7 | 17:51294144 | TACAGTTAATAAATT[C/G]TAGTCTGTTTATCTT | 51096 |
rs1015709 | snp | C/T | 0.264084 | 0.249603 | intron-variant | UTP18 | GRCh38.p7 | 17:51279084 | AATATTGTAACTTAG[C/T]AACTTAAAATTTTAA | 51096 |
rs1019195 | snp | A/G | 0.437118 | 0.165792 | intron-variant | UTP18 | GRCh38.p7 | 17:51278160 | ACTTTGATCCTTTCC[A/G]AGTAGATCCTTGGTT | 51096 |
rs2318787 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | UTP18 | GRCh38.p7 | 17:51270174 | TTTTTCCCCTTCTTC[C/T]CTTTTCTTTAAGAAC | 51096 |
rs2318788 | snp | C/T | 0.43655 | 0.16643 | intron-variant | UTP18 | GRCh38.p7 | 17:51270259 | ACGGTTTGAAACATA[C/T]AGATTATCTTCTTTT | 51096 |
rs2318789 | snp | A/C | 0.496074 | 0.044618 | synonymous-codon | UTP18 | GRCh38.p7 | 17:51273441 | TTCTCTTCCAAGAGG[A/C]ATCTTGAAGGTGAGA | 51096 |
rs3217081 | in-del | -/AG | 0.488846 | 0.0738428 | intron-variant | UTP18 | GRCh38.p7 | 17:51276141 | TCTCACAGAAGTGAC[-/AG]AGTTCATTTACTTGG | 51096 |
rs3217082 | in-del | -/CA | | | downstream-variant-500B | UTP18 | GRCh38.p7 | 17:51297977 | CCAACACACACACAC[-/CA]AAACTTGGATGCATT | 51096 |
rs3786007 | snp | A/G | 0.437542 | 0.165312 | intron-variant | UTP18 | GRCh38.p7 | 17:51274377 | ATCTGTCATACTAAC[A/G]GGCAGTACTTTAGTT | 51096 |
rs3786008 | snp | G/T | 0.110167 | 0.207236 | intron-variant | UTP18 | GRCh38.p7 | 17:51274920 | AGTTACCACATGGCC[G/T]GGCGCAGTGGCTCAC | 51096 |
rs3837855 | in-del | -/T | 0.437401 | 0.165472 | intron-variant | UTP18 | GRCh38.p7 | 17:51275239 | CCATAAAAATTTAAC[-/T]TTGGTGGTTACAAAC | 51096 |
rs4448992 | snp | A/G | 0.437118 | 0.165792 | intron-variant | UTP18 | GRCh38.p7 | 17:51270473 | GATTCCTGTAATTTT[A/G]GGTATGGTTATGCTA | 51096 |
rs4793690 | snp | A/T | 0.486855 | 0.0799975 | intron-variant | UTP18 | GRCh38.p7 | 17:51264049 | TTTTTTTTAATTATT[A/T]TTTTTGAAACAGAGT | 51096 |
rs4793691 | snp | G/T | 0.488905 | 0.0736498 | intron-variant | UTP18 | GRCh38.p7 | 17:51283299 | tcagcctcctgggta[G/T]ctgggattacaggca | 51096 |
rs4793692 | snp | A/C | 0.488905 | 0.0736498 | intron-variant | UTP18 | GRCh38.p7 | 17:51283542 | TTGTTACATGTAAAG[A/C]ATAATTTGAGATAAA | 51096 |
rs4794217 | snp | G/T | 0.493925 | 0.054776 | intron-variant | UTP18 | GRCh38.p7 | 17:51268014 | TGTTTTTTGTTTTTT[G/T]TTTTTTTTTTTTTGA | 51096 |
rs4794218 | snp | C/T | 0.490007 | 0.0699769 | intron-variant | UTP18 | GRCh38.p7 | 17:51270280 | ATCTTCTTTTTCTCT[C/T]ATTTGGGAAGCCTCT | 51096 |
rs4794219 | snp | G/T | 0.437259 | 0.165632 | intron-variant | UTP18 | GRCh38.p7 | 17:51279512 | TTGTTTTTTGTTTTT[G/T]TTTTTGACTCACAAA | 51096 |
rs4794220 | snp | A/G | 0.482534 | 0.0918038 | intron-variant | UTP18 | GRCh38.p7 | 17:51286186 | GCTATTACTGAAAAC[A/G]TTGGTTATTACACTG | 51096 |
rs4794221 | snp | A/T | 0.440609 | 0.161766 | intron-variant, downstream-variant-500B | UTP18 | GRCh38.p7 | 17:51286828 | TTATAAGTAGTTTTT[A/T]AATTTTTTTTATTAT | 51096 |
rs5820850 | in-del | -/T | 0.375 | 0.216506 | intron-variant | UTP18 | GRCh38.p7 | 17:51293503 | AAACATGAGTTGTTG[-/T]TTTTTTTTTTTTTAA | 51096 |
rs6504702 | snp | C/T | 0.490063 | 0.0697833 | intron-variant | UTP18 | GRCh38.p7 | 17:51276948 | TACCTTCTGTTAAGC[C/T]TTTTTATGAAGGCCT | 51096 |
rs6504703 | snp | A/G | 0.43598 | 0.167067 | intron-variant | UTP18 | GRCh38.p7 | 17:51283026 | ggcgcataccgccat[A/G]cccagctaatttttt | 51096 |
rs6504704 | snp | A/G | 0.436692 | 0.166271 | intron-variant | UTP18 | GRCh38.p7 | 17:51283030 | cataccgccataccc[A/G]gctaattttttgtat | 51096 |
rs7210107 | snp | C/G | 0.490119 | 0.0695896 | intron-variant | UTP18 | GRCh38.p7 | 17:51284616 | TGCTTCAGATTTTTG[C/G]TTCAATAATTTATCT | 51096 |
rs7210300 | snp | C/G | 0 | 0 | intron-variant | UTP18 | GRCh38.p7 | 17:51284702 | TTTTTTCCTGTAAAC[C/G]TAAAGGTACTGTCTA | 51096 |
rs7211731 | snp | A/G | 0.184521 | 0.241273 | intron-variant | UTP18 | GRCh38.p7 | 17:51263623 | AGTAGCTAAGAGAAT[A/G]CAGTGTTTGAAGTCA | 51096 |
rs7213331 | snp | A/G | 0.247053 | 0.249983 | intron-variant | UTP18 | GRCh38.p7 | 17:51272980 | TTCATGTGAGTTGTT[A/G]AACTAGATCAGTAGC | 51096 |
rs7215691 | snp | A/G | 0.0659589 | 0.169201 | intron-variant | UTP18 | GRCh38.p7 | 17:51286376 | ACCAAACACAATTGA[A/G]CCATGAAATGATTTC | 51096 |
rs7217151 | snp | C/T | 0.436408 | 0.16659 | intron-variant | UTP18 | GRCh38.p7 | 17:51264902 | tggccaggctggtct[C/T]gaactgttgacctca | 51096 |
rs7502980 | snp | A/G | 0 | 0 | intron-variant | UTP18 | GRCh38.p7 | 17:51273582 | TCATTTTGCCCTGGT[A/G]AATACTTATGTTATT | 51096 |
rs8064307 | snp | C/G | 0.488846 | 0.0738428 | intron-variant | UTP18 | GRCh38.p7 | 17:51271880 | accattttggtcagg[C/G]tggtctcgaactcct | 51096 |
rs8067441 | snp | A/G | 0.0120287 | 0.0766138 | synonymous-codon | UTP18 | GRCh38.p7 | 17:51275985 | TAATGCTGTATCACT[A/G]TTTCAGGTATGCATC | 51096 |
rs8069804 | snp | A/G | 0.261056 | 0.249755 | upstream-variant-2KB, utr-variant-5-prime | UTP18, MBTD1 | GRCh38.p7 | 17:51260442 | GGGAGTTACGTAGAG[A/G]GAGGGAGTGCTGGTC | 51096 |
rs8070746 | snp | A/G | 0.490343 | 0.0688145 | intron-variant | UTP18 | GRCh38.p7 | 17:51268316 | caggcgtgagccatg[A/G]cgcccggccCAGGTA | 51096 |
rs8071800 | snp | C/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51268268 | cctgacctcgtgatc[C/T]gcccgccttggcctc | 51096 |
rs8076189 | snp | A/G | 0.437259 | 0.165632 | intron-variant | UTP18 | GRCh38.p7 | 17:51270640 | AGGTTGGTTCTTCCA[A/G]AGTTGCCTAAGATGT | 51096 |
rs8076318 | snp | C/T | 0.43555 | 0.167544 | intron-variant | UTP18 | GRCh38.p7 | 17:51268314 | tacaggcgtgagcca[C/T]ggcgcccggccCAGG | 51096 |
rs8076463 | snp | C/T | 0.184203 | 0.241186 | intron-variant, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51261736 | GGCGTGTGTAGAGGC[C/T]TGTGAAATTTTAGAT | 51096 |
rs8077559 | snp | G/T | 0.247337 | 0.249986 | intron-variant | UTP18 | GRCh38.p7 | 17:51270308 | TCTTTCCATGTTTGT[G/T]TTTTAATATGTTAAA | 51096 |
rs8078941 | snp | A/G | 0.489024 | 0.0732638 | intron-variant, downstream-variant-500B | UTP18 | GRCh38.p7 | 17:51287073 | CCTCTATATGGGGCA[A/G]GAAAAACTGCGCAGA | 51096 |
rs8078958 | snp | A/C | 0.437542 | 0.165312 | intron-variant, downstream-variant-500B | UTP18 | GRCh38.p7 | 17:51287124 | GTGAAGCCAGTCTTC[A/C]TTGCCCTCTCTTTTT | 51096 |
rs8080145 | snp | C/T | 0.43655 | 0.16643 | intron-variant | UTP18 | GRCh38.p7 | 17:51268536 | CATAGTCCTGATATC[C/T]GGGATGTGTTGATAT | 51096 |
rs8082304 | snp | A/G | 0.184203 | 0.241186 | intron-variant | UTP18 | GRCh38.p7 | 17:51272291 | tttagtagagacggg[A/G]tttctccatgttggc | 51096 |
rs9889715 | snp | C/T | 0.490063 | 0.0697833 | intron-variant | UTP18 | GRCh38.p7 | 17:51273797 | TAATTCTAGGAATCC[C/T]GTTTGGTTTATCTTC | 51096 |
rs9889777 | snp | A/C | 0.429388 | 0.174127 | upstream-variant-2KB, intron-variant | UTP18, MBTD1 | GRCh38.p7 | 17:51259432 | TTCCCCTGCAAAGCA[A/C]CGAAACTGTGCTCCC | 51096 |
rs9891795 | snp | C/T | 0.0463947 | 0.145069 | intron-variant | UTP18 | GRCh38.p7 | 17:51283148 | tgctaggattacagg[C/T]gtgagccaccgcgcc | 51096 |
rs9893020 | snp | A/G | 0.248755 | 0.249997 | intron-variant | UTP18 | GRCh38.p7 | 17:51291749 | atctcaaaaaaaaaa[A/G]aaaagaaaagaaaag | 51096 |
rs9893889 | snp | C/T | 0.192088 | 0.2432 | intron-variant | UTP18 | GRCh38.p7 | 17:51285924 | ATGCTGGCGCTACCT[C/T]ATATCATTGTATTTT | 51096 |
rs9894562 | snp | A/G | 0.0584853 | 0.160693 | intron-variant | UTP18 | GRCh38.p7 | 17:51267382 | gttaggcattttaaa[A/G]tgtaaatttggtggc | 51096 |
rs9896351 | snp | A/G | 0.0345262 | 0.126772 | intron-variant | UTP18 | GRCh38.p7 | 17:51283415 | tcaggtgatctgccc[A/G]ccttggcctcccaaa | 51096 |
rs9897204 | snp | C/T | 0.0663309 | 0.169604 | intron-variant | UTP18 | GRCh38.p7 | 17:51267800 | GGTGatggggttcat[C/T]ttgcttatatccctt | 51096 |
rs9901084 | snp | C/T | 0.489722 | 0.0709447 | intron-variant | UTP18 | GRCh38.p7 | 17:51264690 | TTTAGTCATTGTCTT[C/T]TTTTTTTTTTTTTTG | 51096 |
rs9903174 | snp | A/G | 0.0737376 | 0.17729 | intron-variant | UTP18 | GRCh38.p7 | 17:51280536 | TTTAAATTTTAggcc[A/G]ggcgcggtggctcac | 51096 |
rs9904690 | snp | C/T | 0.0471551 | 0.14613 | intron-variant, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51261463 | TCTGGCAATGGCAAA[C/T]CCTGCGTGATTGATC | 51096 |
rs9906420 | snp | A/C | | | intron-variant | UTP18 | GRCh38.p7 | 17:51269093 | ggagtttaagaccag[A/C]ccgggtgacatggcg | 51096 |
rs9906442 | snp | A/C | | | intron-variant | UTP18 | GRCh38.p7 | 17:51269131 | atctctacaaaaaat[A/C]caaaaattagccagg | 51096 |
rs9906719 | snp | A/C | 0.00956916 | 0.0685055 | intron-variant | UTP18 | GRCh38.p7 | 17:51269255 | taagtgataagtgcc[A/C]ccgtactccagcctg | 51096 |
rs9908910 | snp | C/T | 0.190205 | 0.242744 | intron-variant | UTP18 | GRCh38.p7 | 17:51265760 | gtagagatggtgttt[C/T]accacgttggccaag | 51096 |
rs9911123 | snp | A/G | 0.154865 | 0.231191 | intron-variant | UTP18 | GRCh38.p7 | 17:51266297 | TAAGTGTCTTTTTTC[A/G]TATGATTTACCAAGA | 51096 |
rs9911355 | snp | A/G | 0.437259 | 0.165632 | intron-variant | UTP18 | GRCh38.p7 | 17:51269532 | CCTCTCACATCATGT[A/G]GGAGCTCCTTCCTTA | 51096 |
rs10514982 | snp | G/T | 0.253824 | 0.249971 | intron-variant | UTP18 | GRCh38.p7 | 17:51271203 | TGGCTTGATGTCTTC[G/T]GTAAGTTTTGGAAAT | 51096 |
rs10604907 | in-del | -/CT | 0.437824 | 0.164991 | intron-variant | UTP18 | GRCh38.p7 | 17:51267960 | AAAAAATTAAAACAA[-/CT]CTCTTTGCCCTCTTC | 51096 |
rs10695281 | in-del | -/TT | 0 | 0 | intron-variant | UTP18 | GRCh38.p7 | 17:51265583 | TTTTTTTTTTTTTTT[-/TT]GAGACAGTCTCACTC | 51096 |
rs10853118 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | UTP18 | GRCh38.p7 | 17:51269595 | TTATGACCACCTCCT[C/T]TGTCCCCTTTCTTCC | 51096 |
rs11079951 | snp | C/T | 0.48818 | 0.0759629 | intron-variant | UTP18 | GRCh38.p7 | 17:51265326 | TAGAGTGTAGTGGTG[C/T]GATCTTGGCTCACTG | 51096 |
rs11079952 | snp | C/G | 0.488965 | 0.0734569 | intron-variant | UTP18 | GRCh38.p7 | 17:51268393 | TTTCCAGAGTGAAGT[C/G]ATTCTGTTTTATTCA | 51096 |
rs11079953 | snp | A/G | 0.488905 | 0.0736498 | intron-variant | UTP18 | GRCh38.p7 | 17:51269096 | GTTTAAGACCAGACC[A/G]GGTGACATGGCGAAA | 51096 |
rs11397806 | in-del | -/C/CC | 0.5 | 0.000399361 | intron-variant, downstream-variant-500B | UTP18 | GRCh38.p7 | 17:51286978 | CCCCCTTCCCCCCCC[-/C/CC]GACCCACAGGCCCCG | 51096 |
rs11657473 | snp | A/C | | | intron-variant | UTP18 | GRCh38.p7 | 17:51269315 | aaaaaaaaaaaaaaa[A/C]aaaaaaaaaAACCAA | 51096 |
rs11867403 | snp | G/T | 0.482384 | 0.0921818 | downstream-variant-500B | UTP18 | GRCh38.p7 | 17:51298290 | TCTGGCCTTATTACT[G/T]CAAATCTTTGTCATT | 51096 |
rs12453696 | snp | A/G | 0.245346 | 0.249957 | downstream-variant-500B | UTP18 | GRCh38.p7 | 17:51298324 | ATTTGAAGAGGAGCC[A/G]TAGTAAACCTGGTAG | 51096 |
rs12937109 | snp | G/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51274758 | gcccagcGACATAGG[G/T]CTCTTTTCTTATTAC | 51096 |
rs12937608 | snp | G/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51274881 | TTAGCTCTTTACGGG[G/T]GAATTCACCTCCATT | 51096 |
rs12937624 | snp | A/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51274902 | CACCTCCATTAAAAA[A/T]GTAGTTACCACATgg | 51096 |
rs12940196 | snp | C/G | 0.496036 | 0.0443428 | intron-variant | UTP18 | GRCh38.p7 | 17:51293869 | CATGAGCTCCCAGTT[C/G]TTACACTTTAAAGTT | 51096 |
rs12941969 | snp | A/C | 0 | 0 | intron-variant, missense | UTP18 | GRCh38.p7 | 17:51286563 | GAAAGGCAAGTAGAA[A/C]TAGGCTGTGGAGCTT | 51096 |
rs12943945 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51274756 | gcgcccagcGACATA[A/G]GTCTCTTTTCTTATT | 51096 |
rs12947643 | snp | A/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51274909 | ATTAAAAATGTAGTT[A/T]CCACATggccgggcg | 51096 |
rs12948421 | snp | A/G | 0.488545 | 0.074807 | intron-variant | UTP18 | GRCh38.p7 | 17:51290776 | TAAAAGCCAAATCAC[A/G]GTTTTTAAATGGTAG | 51096 |
rs12951150 | snp | C/G | 0.488118 | 0.0761554 | intron-variant | UTP18 | GRCh38.p7 | 17:51264768 | GCTCACTGCAACCTC[C/G]GCCTCCCAGGTTCAA | 51096 |
rs16949739 | snp | A/G | 0.184521 | 0.241273 | intron-variant | UTP18 | GRCh38.p7 | 17:51269688 | ATAATTCTATTAGAA[A/G]AGACAATCTGTTACT | 51096 |
rs16949746 | snp | G/T | 0.0248432 | 0.108648 | intron-variant | UTP18 | GRCh38.p7 | 17:51276721 | GTATCTGCTCTTGGA[G/T]AGGGTATCCCAGTTT | 51096 |
rs16949750 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | UTP18 | GRCh38.p7 | 17:51279351 | TATGAACCTTTCAGT[C/T]ATGGAAAAAGAGACA | 51096 |
rs16949752 | snp | A/G | 0.0490535 | 0.14873 | intron-variant | UTP18 | GRCh38.p7 | 17:51280214 | TCTCCAAGTAGAGGA[A/G]CACAGGTGGGACTTG | 51096 |
rs16949753 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | UTP18 | GRCh38.p7 | 17:51282067 | GTTAACTCTTACTGT[C/T]TATCCCAAAGGACCA | 51096 |
rs16949758 | snp | A/G | 0.0433465 | 0.140692 | intron-variant, synonymous-codon | UTP18 | GRCh38.p7 | 17:51286675 | TTCCTACCCATACCC[A/G]TGCCAACCCTGTAGC | 51096 |
rs17575641 | snp | A/G | 0.267908 | 0.249358 | intron-variant | UTP18 | GRCh38.p7 | 17:51293134 | TGATCAGATTTTAGT[A/G]TTCTTTACTGTGGTC | 51096 |
rs28379319 | snp | C/T | 0.021895 | 0.102314 | synonymous-codon | UTP18 | GRCh38.p7 | 17:51263276 | TTGTCTGCTGTAGGT[C/T]CAAGAACATGAAGAC | 51096 |
rs28459876 | snp | C/T | 0.0737376 | 0.17729 | intron-variant | UTP18 | GRCh38.p7 | 17:51273906 | TTTACTTCTACTTTA[C/T]CTCTTTTTAAATCAT | 51096 |
rs34049859 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51276329 | GTATGACTTCAGTGT[A/G]CAAGGAACCATAATA | 51096 |
rs34103760 | in-del | -/TT/TTT | 0.479663 | 0.0987666 | intron-variant | UTP18 | GRCh38.p7 | 17:51283617 | TTTTTTTTTTTTTTT[-/TT/TTT]GGAGACAGCATTGCT | 51096 |
rs34113761 | in-del | -/C | | | intron-variant | UTP18 | GRCh38.p7 | 17:51291595 | AAAAATTAGCTGGGC[-/C]GTGGTAGCCCACACC | 51096 |
rs34120435 | in-del | -/C | | | intron-variant | UTP18 | GRCh38.p7 | 17:51296741 | TTTCATAGACCCCCC[-/C]ATGTGAAACTTTGGA | 51096 |
rs34207677 | snp | G/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51262512 | CCAGACTGGAGTGTA[G/T]CGGCACCTATTAGTC | 51096 |
rs34301015 | snp | C/T | 0.487995 | 0.0765403 | intron-variant | UTP18 | GRCh38.p7 | 17:51262740 | AATTTTCTGTAGAGA[C/T]GAGATCTCCCTATGT | 51096 |
rs34328363 | in-del | -/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51281215 | TTTCTTTTTAGCTAG[-/T]AAAATCAGATCTATT | 51096 |
rs34329392 | in-del | -/C | | | intron-variant | UTP18 | GRCh38.p7 | 17:51294495 | AGAATGATGGTTTCC[-/C]AGTTTCATCCATGTC | 51096 |
rs34350123 | in-del | -/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51288354 | AGCTTTTGGATGTGG[-/G]TTGTTGGAAGGATGC | 51096 |
rs34411162 | in-del | -/C | | | intron-variant | UTP18 | GRCh38.p7 | 17:51272450 | CGTTGTTTAGATCCC[-/C]TGTGGGGATTGTCTG | 51096 |
rs34538423 | in-del | -/TT | | | intron-variant, downstream-variant-500B | UTP18 | GRCh38.p7 | 17:51289213 | TTGTTTTTTTTTTTT[-/TT]GAGACCAAGTCTCAC | 51096 |
rs34709162 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51265001 | TTTCTTATAAATATT[C/G]TTTATTATGTCCTTG | 51096 |
rs34733370 | in-del | -/G | | | intron-variant, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51262483 | ATTTAGAGATACGGT[-/G]CTAACTTTGTCACCC | 51096 |
rs34835378 | multinucleotide-polymorphism | AC/GG | 0.5 | 0 | intron-variant | UTP18 | GRCh38.p7 | 17:51274138 | TTGGACATGCTGCTA[AC/GG]TCCTTTCTTGCCTGT | 51096 |
rs35125986 | snp | A/G | 0.039522 | 0.134904 | intron-variant | UTP18 | GRCh38.p7 | 17:51276475 | TCTCTCTACAAAAAC[A/G]TGTTCTTTTAATTTT | 51096 |
rs35246329 | in-del | -/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51264607 | TATTTGTTTTTTTTT[-/T]CCAGACTCTGTCAGT | 51096 |
rs35339154 | in-del | -/C | 0.490175 | 0.0693959 | intron-variant | UTP18 | GRCh38.p7 | 17:51264608 | ATTTGTTTTTTTTTT[-/C]CAGACTCTGTCAGTT | 51096 |
rs35339641 | in-del | -/T | 0.409212 | 0.192748 | intron-variant | UTP18 | GRCh38.p7 | 17:51273186 | TCTTCTCCTTTAAAA[-/T]TTTTTTTTTTTTTTT | 51096 |
rs35392353 | in-del | -/A | | | intron-variant, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51262109 | TTTTTTTTTTTTAGA[-/A]CTCGCCCTGTCGCCC | 51096 |
rs35572092 | in-del | -/C | | | intron-variant | UTP18 | GRCh38.p7 | 17:51272298 | AGACGGGGTTTCTCC[-/C]ATGTTGGCCAGGTTG | 51096 |
rs35639364 | in-del | -/C | | | intron-variant | UTP18 | GRCh38.p7 | 17:51294558 | GCTGCATAGTATTCC[-/C]ATGGTGTATATGTGC | 51096 |
rs35859373 | in-del | -/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51279346 | GTCAATATGAACCTT[-/T]CAGTCATGGAAAAAG | 51096 |
rs35962209 | in-del | -/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51288507 | TTAAGGCAGACACTT[-/T]CATTCCTTCACAATT | 51096 |
rs35995271 | in-del | -/G | | | intron-variant, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51262441 | AACTTTAGAATTTAG[-/G]ATTTAATGGTATATT | 51096 |
rs36097713 | in-del | -/T | 0.493568 | 0.0563433 | intron-variant | UTP18 | GRCh38.p7 | 17:51273598 | TTGTTTTTTTTTTTT[-/T]CCTTTTGCAAAAAAT | 51096 |
rs55638604 | snp | C/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51283249 | TCTCGCCTCACTGCA[C/G]CCTCTGCCTCCTGGG | 51096 |
rs56286676 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant, utr-variant-3-prime | UTP18 | GRCh38.p7 | 17:51286779 | TCTTCTGGGAATAAA[C/G]CTCCTTTAAAATGAA | 51096 |
rs56302947 | snp | G/T | 0.483636 | 0.0889627 | intron-variant, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51262185 | TTCCTGGGTTCAAGC[G/T]ATTCTCCTGCCTCAG | 51096 |
rs56715470 | snp | A/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51292447 | TATTTTCTTGACAAA[A/T]TGGTCAGTAAGTATG | 51096 |
rs57046248 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | UTP18 | GRCh38.p7 | 17:51286130 | CCATTTGATAGTATT[A/G]TAGAAACTTTAAAAA | 51096 |
rs57164982 | snp | A/T | 0.499104 | 0.0211472 | intron-variant | UTP18 | GRCh38.p7 | 17:51281164 | TATATATATATATAT[A/T]TTTTTTTTAAACGAA | 51096 |
rs57303510 | in-del | -/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51288241 | TTATTGTTATTTTTT[-/T]AAATTTAAGTTGAAA | 51096 |
rs57322775 | in-del | -/CA | 0.5 | 0 | downstream-variant-500B | UTP18 | GRCh38.p7 | 17:51297978 | CAACACACACACACA[-/CA]AACTTGGATGCATTT | 51096 |
rs57683372 | in-del | -/C | 0.247053 | 0.249983 | intron-variant | UTP18 | GRCh38.p7 | 17:51290163 | GCTCAGACCTGTAAT[-/C]CCGGCACTTTGGGAG | 51096 |
rs57818544 | snp | A/G | 0.0441095 | 0.141807 | intron-variant | UTP18 | GRCh38.p7 | 17:51281288 | AGTGGAGGACTAACA[A/G]TTTAACATGCAGTTT | 51096 |
rs58023022 | snp | C/G | 0.0722614 | 0.17581 | intron-variant | UTP18 | GRCh38.p7 | 17:51281221 | TTTTAGCTAGAAAAT[C/G]AGATCTATTTTTAGA | 51096 |
rs58180688 | in-del | -/GT/TG | | | intron-variant | UTP18 | GRCh38.p7 | 17:51269860 | TGTGTGTGTGTGTGT[-/GT/TG]CAGTGTCAGAATCTC | 51096 |
rs58255126 | snp | C/G | 0.488786 | 0.0740357 | intron-variant | UTP18 | GRCh38.p7 | 17:51274139 | TGGACATGCTGCTAG[C/G]TCCTTTCTTGCCTGT | 51096 |
rs58446664 | in-del | -/GGAA | 0.436408 | 0.16659 | intron-variant | UTP18 | GRCh38.p7 | 17:51282508 | GAAGGAAGGAAAGAT[-/GGAA]GGAAGGAAGGAAGGA | 51096 |
rs58674308 | in-del | -/TT/TTT | 0.5 | 0 | intron-variant, downstream-variant-500B | UTP18 | GRCh38.p7 | 17:51289371 | TTTTTTTTTTTTTTT[-/TT/TTT]AAGTAGAGACGGGGT | 51096 |
rs58681434 | in-del | -/AAAAAAA | | | intron-variant | UTP18 | GRCh38.p7 | 17:51269320 | AAAAAAAAAAAAAAA[-/AAAAAAA]CCAAAAAAATCTGTT | 51096 |
rs58879155 | snp | A/G | 0.0770498 | 0.180522 | intron-variant | UTP18 | GRCh38.p7 | 17:51269108 | ACCGGGTGACATGGC[A/G]AAACCCCATCTCTAC | 51096 |
rs58946658 | in-del | -/AAATAAATAAAT/AAATAAATAAATAAAT | 0 | 0 | intron-variant | UTP18 | GRCh38.p7 | 17:51273774 | AATAAATAAATAAAT[lengthTooLong]TTTCCAGTAATTCTA | 51096 |
rs59041584 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51292501 | GACTGACTGAAACCA[A/G]TTTAATAGGTGTATG | 51096 |
rs59154294 | snp | A/T | 0.452842 | 0.146134 | intron-variant | UTP18 | GRCh38.p7 | 17:51281162 | TATATATATATATAT[A/T]TATTTTTTTTAAACG | 51096 |
rs59599486 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant, downstream-variant-500B | UTP18 | GRCh38.p7 | 17:51286874 | GGTACATGTGCATAA[C/T]GTGCAGGTTTGTTAC | 51096 |
rs59857038 | in-del | -/ATATATT/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51281165 | TATATATATATATAT[-/ATATATT/T]TTTTTTTAAACGAAA | 51096 |
rs60173307 | snp | A/G | 0.488786 | 0.0740357 | intron-variant | UTP18 | GRCh38.p7 | 17:51274138 | TTGGACATGCTGCTA[A/G]GTCCTTTCTTGCCTG | 51096 |
rs60624309 | snp | A/T | 0.00716266 | 0.059414 | intron-variant | UTP18 | GRCh38.p7 | 17:51295417 | TCAGCTTTCTACATA[A/T]GGCTAGCCAGTTTTC | 51096 |
rs61700935 | snp | G/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51292448 | ATTTTCTTGACAAAA[G/T]GGTCAGTAAGTATGT | 51096 |
rs61732669 | snp | C/T | 0.00292198 | 0.038111 | missense | UTP18 | GRCh38.p7 | 17:51288139 | GTGTTACTTCTCTGA[C/T]CTTCAATCCTACTAC | 51096 |
rs62060087 | snp | A/C | 0.265453 | 0.249522 | upstream-variant-2KB, intron-variant | UTP18, MBTD1 | GRCh38.p7 | 17:51259413 | CCCAAGGCAGATAGA[A/C]ACCTTCCCCTGCAAA | 51096 |
rs62060088 | snp | A/G | 0.26326 | 0.249648 | intron-variant | UTP18 | GRCh38.p7 | 17:51268183 | GGCACCTGCCAACAC[A/G]CCCAGCTAATTTTTT | 51096 |
rs62060089 | snp | G/T | 0.263809 | 0.249618 | intron-variant | UTP18 | GRCh38.p7 | 17:51269839 | ATATCAAATAATGTA[G/T]TGTGTGTGTGTGTGT | 51096 |
rs62060090 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | UTP18 | GRCh38.p7 | 17:51270510 | GAAACAAAATCCCAC[A/G]GATCCCAGTGGCATA | 51096 |
rs62060092 | snp | C/T | 0.263535 | 0.249633 | intron-variant | UTP18 | GRCh38.p7 | 17:51295341 | GTTTTAGGTCTAACA[C/T]GTAAGTCTTTAATCC | 51096 |
rs67272123 | in-del | ATA/TT | 0.5 | 0 | intron-variant | UTP18 | GRCh38.p7 | 17:51281162 | TATATATATATATAT[ATA/TT]TTTTTTTTTAAACGA | 51096 |
rs71149358 | in-del | -/C | 0 | 0 | intron-variant | UTP18 | GRCh38.p7 | 17:51269328 | AAAAAAAAAAAAACC[-/C]AAAAAAATCTGTTTT | 51096 |
rs71355747 | in-del | -/TT | 0.5 | 0 | intron-variant | UTP18 | GRCh38.p7 | 17:51265563 | CCACCGTGCCCGGCC[-/TT]TTTTTTTTTTTTTTT | 51096 |
rs71355749 | in-del | -/A/AATA/AATAAATAAATA/AATAAATAAATAAATA | 0.5 | 0 | intron-variant | UTP18 | GRCh38.p7 | 17:51273739 | CCCTGTCTCTAAAAT[lengthTooLong]AATAAATAAATAAAT | 51096 |
rs71355750 | in-del | -/T | 0.5 | 0 | intron-variant | UTP18 | GRCh38.p7 | 17:51274477 | GACAGAGTTTTGCTC[-/T]TTTGCTCAGGCTGGA | 51096 |
rs71355752 | in-del | -/A | 0.5 | 0 | intron-variant | UTP18 | GRCh38.p7 | 17:51283430 | CCTTGGCCTCCCAAA[-/A]GTGCTGGGATTATAG | 51096 |
rs71355753 | in-del | -/TT | 0.375 | 0.216506 | intron-variant, downstream-variant-500B | UTP18 | GRCh38.p7 | 17:51289201 | TTTCTGTTTTTTTTG[-/TT]TTTTTTTTTTTTGAG | 51096 |
rs71356546 | multinucleotide-polymorphism | CGA/TGG | 0.5 | 0 | intron-variant | UTP18 | GRCh38.p7 | 17:51268314 | TACAGGCGTGAGCCA[CGA/TGG]CGCCCGGCCCAGGTA | 51096 |
rs71866950 | in-del | -/GT | 0.120112 | 0.21361 | intron-variant | UTP18 | GRCh38.p7 | 17:51267403 | ATTTGGTGGCATTTA[-/GT]ATATTTAGAATGTTG | 51096 |
rs72261415 | in-del | -/AC | 0.490175 | 0.0693959 | downstream-variant-500B | UTP18 | GRCh38.p7 | 17:51297965 | TTCCCTCCACCCCCA[-/AC]ACACACACACACAAA | 51096 |
rs72826493 | snp | A/T | 0.0240643 | 0.107019 | intron-variant | UTP18 | GRCh38.p7 | 17:51270209 | AGACAGTTTTTCCTA[A/T]TTTGAAATGTATGTC | 51096 |
rs72826501 | snp | A/G | 0.0283406 | 0.115616 | intron-variant | UTP18 | GRCh38.p7 | 17:51286239 | CTACTTGATTCTGAA[A/G]ATGCAGGGTGAGAGG | 51096 |
rs73334961 | snp | A/G | 0.067446 | 0.170804 | intron-variant, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51262415 | AGTATAAACTTTATG[A/G]TATAAATTTATAACT | 51096 |
rs73334962 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | UTP18 | GRCh38.p7 | 17:51262641 | CAGCTTCATCCTCCT[A/G]GGCTCAAGTGATCCT | 51096 |
rs73334981 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | UTP18 | GRCh38.p7 | 17:51274302 | TTCTAACTCATCACT[A/G]TGTCTAGCATGTTCA | 51096 |
rs73337638 | snp | G/T | 0.0333695 | 0.124785 | intron-variant | UTP18 | GRCh38.p7 | 17:51290461 | TGCTGGAAAAAGAGT[G/T]TGAAAATTACAGCAT | 51096 |
rs73337641 | snp | A/G | 0.0659589 | 0.169201 | intron-variant | UTP18 | GRCh38.p7 | 17:51295804 | GCAGTACTTTGGGTA[A/G]TTTTCTACCATAAAA | 51096 |
rs73988585 | snp | C/T | 0.01826 | 0.09379 | intron-variant | UTP18 | GRCh38.p7 | 17:51266294 | GAGTAAGTGTCTTTT[C/T]TCATATGATTTACCA | 51096 |
rs74332677 | snp | C/T | 0.0337553 | 0.125452 | intron-variant | UTP18 | GRCh38.p7 | 17:51273256 | ATTGAGGTAGGGAGG[C/T]TGGAAAGGGAGTTGA | 51096 |
rs74411438 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | UTP18 | GRCh38.p7 | 17:51292398 | GGCAAAGTTGAAAAT[A/C]ATTGAATGTGGCTTG | 51096 |
rs74433176 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51261334 | CACGGGCCTGGGCAT[C/T]TCCGTTGTAACTATG | 51096 |
rs74482578 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51285533 | TTTATCATCTTTGTG[C/G/T]AGTGTTGAATAATAA | 51096 |
rs74678447 | snp | A/G | 0.0479149 | 0.147179 | intron-variant, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51261907 | CAGAACTATTACTGG[A/G]AACATGCTGAACTGT | 51096 |
rs74708191 | snp | A/T | 0.5 | 0 | intron-variant | UTP18 | GRCh38.p7 | 17:51293516 | TGTTTTTTTTTTTTT[A/T]AAGCTCATCACCTGT | 51096 |
rs74775520 | snp | C/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51292620 | CCAGCTGAATGATAA[C/T]GGTTGTATATATTTG | 51096 |
rs74789717 | snp | G/T | 0.5 | 0 | intron-variant | UTP18 | GRCh38.p7 | 17:51293503 | AAACATGAGTTGTTG[G/T]TTTTTTTTTTTTTAA | 51096 |
rs74927806 | snp | A/G | 0.187053 | 0.241946 | intron-variant | UTP18 | GRCh38.p7 | 17:51281796 | GTGTGAATCTAAAAG[A/G]CATAATTTTAAATAA | 51096 |
rs74945395 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | UTP18 | GRCh38.p7 | 17:51272421 | AGTATTTTTAAGGTT[C/T]GTGTCTGATAATTCC | 51096 |
rs75030176 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | UTP18 | GRCh38.p7 | 17:51274109 | CTTGAGTCACACAAG[C/T]CTTTTTCTGTTTCTT | 51096 |
rs75046713 | snp | A/G | | | missense | UTP18 | GRCh38.p7 | 17:51294017 | TACTTTGCCTTGGGG[A/G]ATGAAAAGGGCAAGG | 51096 |
rs75230618 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | UTP18 | GRCh38.p7 | 17:51270169 | ACTGTTTTTTCCCCT[C/T]CTTCCCTTTTCTTTA | 51096 |
rs75503423 | snp | G/T | 0.5 | 0 | intron-variant | UTP18 | GRCh38.p7 | 17:51268027 | TTGTTTTTTTTTTTT[G/T]GAGATGGAGCCTGGC | 51096 |
rs75554771 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | UTP18 | GRCh38.p7 | 17:51263520 | AAGTATAGAAAAGAT[C/T]TTTCATGGTTCCTGA | 51096 |
rs75631393 | snp | G/T | 0.5 | 0 | intron-variant | UTP18 | GRCh38.p7 | 17:51265281 | CTTTTTTTTTTTTTT[G/T]AGATGGAGTTTTGCT | 51096 |
rs75833043 | snp | C/T | 0.5 | 0 | intron-variant | UTP18 | GRCh38.p7 | 17:51273200 | ATTTTTTTTTTTTTT[C/T]TCCTGTTTTGCTTTT | 51096 |
rs75845214 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant, downstream-variant-500B | UTP18 | GRCh38.p7 | 17:51289621 | TAATCTTCAGGCAGA[A/G]CCAATTTTCTCATTC | 51096 |
rs75888437 | snp | C/G | 0.0729998 | 0.176553 | intron-variant | UTP18 | GRCh38.p7 | 17:51276426 | ATAATAGATTGAGAA[C/G]TGAAGAATATATTAA | 51096 |
rs75983132 | snp | C/G | 0.0119091 | 0.0762411 | intron-variant | UTP18 | GRCh38.p7 | 17:51276616 | ACAACAGACCTGGCC[C/G]TTCACTTCAGGATGT | 51096 |
rs76018838 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51290551 | AGTCAGCTTTAAAAT[A/C]CCTGCTCCCTAATGG | 51096 |
rs76048054 | snp | C/T | 0.0733688 | 0.176922 | intron-variant | UTP18 | GRCh38.p7 | 17:51296327 | TTCCTGCTTTCAAAA[C/T]GGACTAAAATCTGGA | 51096 |
rs76279225 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | UTP18 | GRCh38.p7 | 17:51268542 | CCTGATATCTGGGAT[A/G]TGTTGATATGAACAA | 51096 |
rs76333499 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UTP18 | GRCh38.p7 | 17:51270816 | TTTGGCTTTGTGCAC[A/G]GGAGAAAAAGGAAGT | 51096 |
rs76719651 | snp | G/T | 0 | 0 | intron-variant | UTP18 | GRCh38.p7 | 17:51275733 | TTTGTTTTTTTTTTT[G/T]GAGTTGTGTTTGGTT | 51096 |
rs76756338 | snp | G/T | 0.5 | 0 | intron-variant, downstream-variant-500B | UTP18 | GRCh38.p7 | 17:51289201 | TTTCTGTTTTTTTTG[G/T]TTTTTTTTTTTTTGA | 51096 |
rs76779333 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | UTP18 | GRCh38.p7 | 17:51270563 | CAGCACATAAAATTG[G/T]GGTGGTAGGAAGGTG | 51096 |
rs77002893 | snp | A/C | 0 | 0 | intron-variant | UTP18 | GRCh38.p7 | 17:51285062 | GAAAAACTGCATCTC[A/C]AAAAAAAAAAAAGGA | 51096 |
rs77139591 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UTP18 | GRCh38.p7 | 17:51272598 | TTTATATGTTTACTT[C/T]TAGGTAGGTAGCTTG | 51096 |
rs77366127 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51282011 | CTTTTGATTAACCTG[C/G]ACTGTCCTGCTCTTC | 51096 |
rs77409176 | snp | C/T | 0.494272 | 0.053207 | intron-variant | UTP18 | GRCh38.p7 | 17:51264608 | ATTTGTTTTTTTTTT[C/T]CAGACTCTGTCAGTT | 51096 |
rs77470377 | snp | G/T | 0 | 0 | intron-variant | UTP18 | GRCh38.p7 | 17:51267474 | TGGTTTTTTTTTTTT[G/T]GGTTCTTAAACATTT | 51096 |
rs77492081 | snp | A/T | 0 | 0 | intron-variant, downstream-variant-500B | UTP18 | GRCh38.p7 | 17:51289374 | GCTCATTTTTGTATT[A/T]TTTTTTTTTTTTTAA | 51096 |
rs77513438 | snp | A/C | | | intron-variant | UTP18 | GRCh38.p7 | 17:51266443 | TTAGGGGAGAGGGGA[A/C]AAAACACAGACACAA | 51096 |
rs77581112 | snp | G/T | 0.5 | 0 | intron-variant, downstream-variant-500B | UTP18 | GRCh38.p7 | 17:51289215 | GTTTTTTTTTTTTTT[G/T]AGACCAAGTCTCACT | 51096 |
rs77637737 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | UTP18 | GRCh38.p7 | 17:51282156 | AGCGGGAGACTTTCA[A/G]GTGGTTCTGCTCTGT | 51096 |
rs77796392 | snp | C/T | 0.0777841 | 0.181223 | intron-variant | UTP18 | GRCh38.p7 | 17:51293483 | CTAATTTGTAAACTT[C/T]CTTAAAACATGAGTT | 51096 |
rs77802867 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | UTP18 | GRCh38.p7 | 17:51270188 | CCCTTTTCTTTAAGA[A/G]CTGTTAGACAGTTTT | 51096 |
rs78081679 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | UTP18 | GRCh38.p7 | 17:51276712 | TGCTTCACAGTATCT[C/G]CTCTTGGATAGGGTA | 51096 |
rs78159834 | snp | C/T | 0.5 | 0 | intron-variant | UTP18 | GRCh38.p7 | 17:51296601 | AGTGAAATTTTTTTT[C/T]CTCTAAGACCCAAAG | 51096 |
rs78192756 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | UTP18 | GRCh38.p7 | 17:51266815 | ATGTTAGTTTCTCCA[A/G]TTGTTGTAAGGTGCA | 51096 |
rs78308324 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UTP18 | GRCh38.p7 | 17:51270282 | CTTCTTTTTCTCTCA[C/T]TTGGGAAGCCTCTTT | 51096 |
rs78558993 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UTP18 | GRCh38.p7 | 17:51272809 | AGTTTTTCCCTTCTT[A/G]GCTCCGCAAGTGTTT | 51096 |
rs78572939 | snp | C/T | 0.0486741 | 0.148216 | intron-variant | UTP18 | GRCh38.p7 | 17:51276882 | TGCCTTCTCAGGGCA[C/T]GCCACCTCCTCAGCA | 51096 |
rs78613922 | snp | G/T | 0.0142736 | 0.0832652 | intron-variant | UTP18 | GRCh38.p7 | 17:51274185 | CTCTTTTGTTCTGCC[G/T]GCCTTGTCTTCAGGA | 51096 |
rs78632165 | snp | C/G | 0.5 | 0 | intron-variant | UTP18 | GRCh38.p7 | 17:51267243 | GCTGGGAATACAGAG[C/G]TGAGCCACTGTGCTC | 51096 |
rs78636697 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | UTP18 | GRCh38.p7 | 17:51269518 | AGTCCGGAGTATATC[C/G]TCTCACATCATGTGG | 51096 |
rs78668561 | snp | A/C | 0.5 | 0 | intron-variant | UTP18 | GRCh38.p7 | 17:51275199 | TGAAACCCAGTCTCA[A/C]AAAAAAAAAAAAAAA | 51096 |
rs78781441 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51284589 | GTTACACTAGTGAGT[A/G]GTGTTTTGTTTTGCT | 51096 |
rs78803387 | snp | C/G | | | missense, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51260594 | CTAACGATGCCGCCG[C/G]AGCGGAGGAGACGAA | 51096 |
rs78830933 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | UTP18 | GRCh38.p7 | 17:51272999 | TAGATCAGTAGCCAA[C/G]CTGTTGCCAATTTTG | 51096 |
rs78947674 | snp | A/G | 0.0821764 | 0.185298 | intron-variant | UTP18 | GRCh38.p7 | 17:51287350 | AGGAAGAAAGGACAG[A/G]GAGATGAGCCTTGAG | 51096 |
rs78960043 | snp | C/T | 0.0733688 | 0.176922 | intron-variant | UTP18 | GRCh38.p7 | 17:51288284 | AACAGGAAAGGAGAG[C/T]GTTGAATTATTTTTA | 51096 |
rs78973136 | snp | G/T | 0.5 | 0 | intron-variant | UTP18 | GRCh38.p7 | 17:51268028 | TGTTTTTTTTTTTTT[G/T]AGATGGAGCCTGGCT | 51096 |
rs79214392 | snp | G/T | 0.5 | 0 | intron-variant | UTP18 | GRCh38.p7 | 17:51282887 | TTTTTTTTTTTTTTT[G/T]AGACAGAGTCTCACT | 51096 |
rs79297433 | snp | C/T | 0.5 | 0 | intron-variant | UTP18 | GRCh38.p7 | 17:51273203 | TTTTTTTTTTTTTTC[C/T]TGTTTTGCTTTTGCC | 51096 |
rs79410166 | snp | G/T | 0.248188 | 0.249993 | intron-variant, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51262418 | ATAAACTTTATGGTA[G/T]AAATTTATAACTTTA | 51096 |
rs79422593 | snp | C/G | 0.00993419 | 0.0697739 | intron-variant | UTP18 | GRCh38.p7 | 17:51280256 | TGGGCAGTTGGGGGA[C/G]AGCTTTTGATTACAG | 51096 |
rs79436337 | snp | G/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51295844 | CAGGAAACTTCACCT[G/T]GGGAATATATATATT | 51096 |
rs79439595 | snp | C/T | 0.119978 | 0.213528 | intron-variant, utr-variant-3-prime | UTP18 | GRCh38.p7 | 17:51288691 | AGGAATCCGCAGGAC[C/T]ACCTCCAGGTTTGGT | 51096 |
rs79505713 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | UTP18 | GRCh38.p7 | 17:51290898 | ATTCCTTATAATGAT[C/G]TAGACGGTTTTGTCA | 51096 |
rs79520268 | snp | C/T | 0.00279162 | 0.0372561 | downstream-variant-500B | UTP18 | GRCh38.p7 | 17:51298200 | GGCTTGATATGAGAG[C/T]AGTGAAATCTCACGT | 51096 |
rs79607053 | snp | C/G | | | intron-variant, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51262003 | ATTAGACTAGTAGTA[C/G]AGCAAGTAGAAACCA | 51096 |
rs79652514 | in-del | -/ATT | | | intron-variant | UTP18 | GRCh38.p7 | 17:51267001 | CCTTAATTTTTAAAA[-/ATT]TTTTTTTGTAGGAAT | 51096 |
rs79657844 | snp | G/T | 0 | 0 | intron-variant | UTP18 | GRCh38.p7 | 17:51265582 | TTTTTTTTTTTTTTT[G/T]TGAGACAGTCTCACT | 51096 |
rs79683944 | snp | C/T | 0.00716266 | 0.059414 | intron-variant, downstream-variant-500B | UTP18 | GRCh38.p7 | 17:51289537 | ATAGCAGCCTTGGGC[C/T]TATGTAAACTCTTTT | 51096 |
rs80026188 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | UTP18 | GRCh38.p7 | 17:51267288 | TTTTAAGTGTTCAGA[C/T]CTGTTGTCTTGTAGA | 51096 |
rs80091502 | snp | G/T | 0 | 0 | intron-variant | UTP18 | GRCh38.p7 | 17:51283632 | ATTTTTTTTTTTTTT[G/T]GGAGACAGCATTGCT | 51096 |
rs80099487 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | UTP18 | GRCh38.p7 | 17:51272696 | TGGGAAGATTTTCTT[A/T]TAATTCTTTGATTTC | 51096 |
rs80188836 | snp | A/C | 0.5 | 0 | intron-variant | UTP18 | GRCh38.p7 | 17:51275200 | GAAACCCAGTCTCAA[A/C]AAAAAAAAAAAAAAG | 51096 |
rs80274222 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | UTP18 | GRCh38.p7 | 17:51262582 | TTGTTGGTCACAGAT[A/G]AATTACACCTGCACA | 51096 |
rs80284546 | snp | G/T | 0.5 | 0 | intron-variant, downstream-variant-500B | UTP18 | GRCh38.p7 | 17:51289213 | TTGTTTTTTTTTTTT[G/T]TGAGACCAAGTCTCA | 51096 |
rs111327061 | snp | A/G | 0.5 | 0 | intron-variant | UTP18 | GRCh38.p7 | 17:51265020 | ATTATGTCCTTGTCT[A/G]TTGGAGACTTTTTAA | 51096 |
rs111336279 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | UTP18 | GRCh38.p7 | 17:51283057 | GTATTTTAGTAGAGA[C/T]GGGGTTTTCTTGTGT | 51096 |
rs111371801 | snp | C/G | 0.5 | 0 | intron-variant | UTP18 | GRCh38.p7 | 17:51289784 | TCACTTGGCAAAAAG[C/G]CTTGCATCTGCCATC | 51096 |
rs111459169 | snp | A/G | 0.5 | 0 | intron-variant | UTP18 | GRCh38.p7 | 17:51291160 | GCACTTTGTGAGGCC[A/G]AGGCAGATGGATCAC | 51096 |
rs111548801 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | UTP18 | GRCh38.p7 | 17:51264028 | AGATTTTCTTTTTCC[C/T]TTTTTTTTTTTTTAA | 51096 |
rs111668290 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UTP18 | GRCh38.p7 | 17:51271016 | ATCTGTAAATATTTA[C/T]TGAGTTTCGTTATAA | 51096 |
rs111684070 | snp | A/G | 0.5 | 0 | intron-variant | UTP18 | GRCh38.p7 | 17:51265216 | AGTAGTTAACAGAGA[A/G]AGACAAATGTTTATC | 51096 |
rs111747821 | in-del | -/TG/TT | 0.498693 | 0.0255257 | intron-variant | UTP18 | GRCh38.p7 | 17:51269839 | TATCAAATAATGTAT[-/TG/TT]TGTGTGTGTGTGTGT | 51096 |
rs111829438 | snp | A/C | | | intron-variant | UTP18 | GRCh38.p7 | 17:51271902 | CGAACTCCTGACCTC[A/C]AGTGATCCACTTGCC | 51096 |
rs111936531 | snp | C/G | 0.5 | 0 | intron-variant | UTP18 | GRCh38.p7 | 17:51265879 | AGGTTTGCTCTTTAT[C/G]TATTTAACTCTTTGA | 51096 |
rs111974255 | snp | A/G | 0.5 | 0 | intron-variant | UTP18 | GRCh38.p7 | 17:51285684 | CTTTTATTAGGATAT[A/G]TTGTTACAATTGTTC | 51096 |
rs111987558 | snp | G/T | 0.5 | 0 | intron-variant | UTP18 | GRCh38.p7 | 17:51296538 | ATAAAAGGATGCAGA[G/T]TCTTATTGCACTTAG | 51096 |
rs112011551 | in-del | -/G | 0.00159617 | 0.0282053 | intron-variant | UTP18 | GRCh38.p7 | 17:51284778 | CAAGAAATATTCTTA[-/G]GGCCGGGCATGGTGG | 51096 |
rs112136037 | snp | G/T | 0.5 | 0 | intron-variant | UTP18 | GRCh38.p7 | 17:51271935 | GGCCTCCCAAAGTAC[G/T]GGAATTACAGATATG | 51096 |
rs112137478 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UTP18 | GRCh38.p7 | 17:51290709 | GCTTCAGTGATCATG[A/G]CAGCATTTATATTTT | 51096 |
rs112147878 | snp | A/T | 0.0115144 | 0.0749975 | intron-variant | UTP18 | GRCh38.p7 | 17:51278023 | ATGTGGCTGGAAAGG[A/T]CAAGAGTAGCTCTGT | 51096 |
rs112244822 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UTP18 | GRCh38.p7 | 17:51292373 | GCTGTGCAGGCAGAA[C/T]CTGCCTTCTGGCAAA | 51096 |
rs112298710 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | UTP18 | GRCh38.p7 | 17:51271706 | TTAGTCTTGCTCTGT[C/T]GTGTAGGCTGGAGTG | 51096 |
rs112607605 | in-del | -/T | 0 | 0 | intron-variant | UTP18 | GRCh38.p7 | 17:51281162 | ATATATATATATATA[-/T]TATTTTTTTTAAACG | 51096 |
rs113022887 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | UTP18 | GRCh38.p7 | 17:51284467 | CCCGTGTTCTGGATC[C/T]GTTCATTTTTCACTT | 51096 |
rs113252326 | in-del | -/T/TT | 0.5 | 0 | intron-variant | UTP18 | GRCh38.p7 | 17:51279506 | TTTTTTTGTTTTTTG[-/T/TT]TTTTTGTTTTTGACT | 51096 |
rs113364580 | snp | C/G | 0.5 | 0 | intron-variant | UTP18 | GRCh38.p7 | 17:51284029 | TACTGAGAGACTAAT[C/G]TTTAAAACACTTTCC | 51096 |
rs113471450 | snp | C/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51291833 | CAGAAAACCAGCTCC[C/T]CAAACTTCAAAGTCA | 51096 |
rs113543154 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UTP18 | GRCh38.p7 | 17:51290948 | GAATTTAAGCTGTTG[A/G]ACTAGTAGGAGACTC | 51096 |
rs113652666 | snp | A/G | 0.5 | 0 | intron-variant | UTP18 | GRCh38.p7 | 17:51268315 | ACAGGCGTGAGCCAT[A/G]GCGCCCGGCCCAGGT | 51096 |
rs113653008 | snp | C/G | 0.5 | 0 | intron-variant | UTP18 | GRCh38.p7 | 17:51283285 | GCAATTCTCCTGCCT[C/G]AGCCTCCTGGGTAGC | 51096 |
rs113666317 | snp | A/T | 0.5 | 0 | intron-variant | UTP18 | GRCh38.p7 | 17:51282511 | GGAAGGAAAGATGGA[A/T]GGAAGGAAGGAAGGA | 51096 |
rs113724536 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | UTP18 | GRCh38.p7 | 17:51272437 | GTGTCTGATAATTCC[A/G]TTGTTTAGATCCCTG | 51096 |
rs113841947 | in-del | -/ATT | 0.5 | 0 | intron-variant, downstream-variant-500B | UTP18 | GRCh38.p7 | 17:51289633 | AGAGCCAATTTTCTC[-/ATT]CATTTAACAATTTTT | 51096 |
rs113871909 | snp | A/G | 0.5 | 0 | upstream-variant-2KB, utr-variant-5-prime | UTP18, MBTD1 | GRCh38.p7 | 17:51260445 | AGTTACGTAGAGGGA[A/G]GGAGTGCTGGTCACG | 51096 |
rs113942216 | snp | C/T | 0.247053 | 0.249983 | intron-variant | UTP18 | GRCh38.p7 | 17:51294425 | TCATTGTTCAATTCC[C/T]ACCTCTGAGTGAGAA | 51096 |
rs113974024 | snp | G/T | | | intron-variant, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51261080 | CGGAGGGTCGCAGCT[G/T]CGGGTCCCTCGCCTC | 51096 |
rs114131498 | snp | G/T | 0.117188 | 0.211804 | upstream-variant-2KB, utr-variant-5-prime | UTP18, MBTD1 | GRCh38.p7 | 17:51260506 | CCCCGGGGCTTCGGC[G/T]GCGGCGGCCCGCGAG | 51096 |
rs114376272 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UTP18 | GRCh38.p7 | 17:51296612 | TTTTTCTCTAAGACC[C/G]AAAGGCCATTAGATT | 51096 |
rs114388585 | snp | A/T | 0.0130921 | 0.0798413 | intron-variant | UTP18 | GRCh38.p7 | 17:51281238 | GATCTATTTTTAGAA[A/T]TCATTTTTGTTGCCA | 51096 |
rs114754066 | snp | A/G | 0.0588605 | 0.161139 | intron-variant | UTP18 | GRCh38.p7 | 17:51297448 | TAGTTCTGCTGCCCA[A/G]TATTTAAAACCATAG | 51096 |
rs114814945 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UTP18 | GRCh38.p7 | 17:51293110 | CATGTTTAAAATCTC[C/T]TTTCCCTGTGATCAG | 51096 |
rs114867309 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51264537 | TATGGGGCTCTACCA[C/G]TTTGCCTTCCCATTG | 51096 |
rs114869627 | snp | G/T | 0.0209421 | 0.100162 | intron-variant, utr-variant-3-prime | UTP18 | GRCh38.p7 | 17:51289117 | TAGGGAAAGTTTCAT[G/T]CCAGTATAGGAACTG | 51096 |
rs114950565 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | UTP18 | GRCh38.p7 | 17:51264716 | TTTTGAGACTCTCAT[C/G]CTTTCATCCAGGCTG | 51096 |
rs115012936 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | UTP18 | GRCh38.p7 | 17:51279910 | ATTTGAGCCACTTAC[A/G]TATTTTAAAAAGTAA | 51096 |
rs115113339 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | UTP18 | GRCh38.p7 | 17:51271707 | TAGTCTTGCTCTGTC[G/T]TGTAGGCTGGAGTGC | 51096 |
rs115136334 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | UTP18 | GRCh38.p7 | 17:51262604 | ACCTGCACAATTCTC[C/T]GAACACTTTAAACTC | 51096 |
rs115314782 | snp | G/T | 0.0733688 | 0.176922 | intron-variant | UTP18 | GRCh38.p7 | 17:51287918 | ATAGCTGGTCTCTTT[G/T]TAACATGATTCCTGT | 51096 |
rs115419894 | snp | A/G | 0.190205 | 0.242744 | intron-variant | UTP18 | GRCh38.p7 | 17:51269907 | TCACCCAGGGCTGGA[A/G]TGCAGTGGGGCAATC | 51096 |
rs115599974 | snp | A/G | 0.0475351 | 0.146656 | intron-variant | UTP18 | GRCh38.p7 | 17:51282836 | TCTTCCTCTCTCTCC[A/G]CTTCTTCCTCCTTTT | 51096 |
rs115641857 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | UTP18 | GRCh38.p7 | 17:51292780 | TCTCAACTCTCCTGA[A/G]CTTAGGAAGTAGACT | 51096 |
rs115677273 | snp | C/T | 0.0737376 | 0.17729 | intron-variant | UTP18 | GRCh38.p7 | 17:51274477 | GACAGAGTTTTGCTC[C/T]TTTGCTCAGGCTGGA | 51096 |
rs115881342 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | UTP18 | GRCh38.p7 | 17:51279140 | GGCAATATATTCACA[C/T]GGTGTTAAAAATCTA | 51096 |
rs116176997 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51261386 | CACCATGTTTTGAGA[A/G]TGATCGTGTATTCCG | 51096 |
rs116206373 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | UTP18 | GRCh38.p7 | 17:51292886 | TCAGAACAGTTTCAC[C/T]TGGAGTTAGATTTTC | 51096 |
rs116316923 | snp | A/G | 0.0722614 | 0.17581 | upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51260522 | GCGGCGGCCCGCGAG[A/G]GGCCTGGGCGCATGC | 51096 |
rs116592848 | snp | A/C | 0.0130921 | 0.0798413 | intron-variant | UTP18 | GRCh38.p7 | 17:51266522 | TATTGCTTACTTGTT[A/C]ATTTGCATATGGTAC | 51096 |
rs116643519 | snp | A/C | 0.0170251 | 0.090679 | intron-variant | UTP18 | GRCh38.p7 | 17:51286047 | TGGGTTTAAATCTTA[A/C]AGATACCTAAAGCAT | 51096 |
rs116675168 | snp | A/T | 0.00212985 | 0.0325636 | intron-variant | UTP18 | GRCh38.p7 | 17:51268815 | GTTGCCATAAATATA[A/T]TTTTCAAATATTTTT | 51096 |
rs116676531 | snp | A/C/T | 0.00488819 | 0.0492399 | intron-variant | UTP18 | GRCh38.p7 | 17:51273339 | GATTCTAAAGATCAG[A/C/T]CTTCTGGGTTTGTTT | 51096 |
rs116854095 | snp | C/T | 0.0433465 | 0.140692 | intron-variant | UTP18 | GRCh38.p7 | 17:51275769 | TCCAGTGCATTTTTT[C/T]CCTTCATTATAAACT | 51096 |
rs117093534 | snp | A/G | 0.0294145 | 0.117656 | synonymous-codon, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51260632 | GGACCGGAGAACCGG[A/G]GCGAAGCCGAAGCGG | 51096 |
rs117234609 | snp | C/T | 0.0486741 | 0.148216 | intron-variant | UTP18 | GRCh38.p7 | 17:51268450 | TTCTTAACAATCTGG[C/T]CAGTTTCTTTTAGAC | 51096 |
rs117405131 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant, downstream-variant-500B | UTP18 | GRCh38.p7 | 17:51287063 | ACTGCATTTGCCTCT[A/G]TATGGGGCAAGAAAA | 51096 |
rs117565932 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51297576 | GGTCTCCTCAGAGAT[G/T]AATGAATGTTGAGGG | 51096 |
rs117604377 | snp | C/G | 0.00914312 | 0.0669923 | intron-variant | UTP18 | GRCh38.p7 | 17:51285973 | GTTTGATCACATCAA[C/G]TTTTCCTATAATTAT | 51096 |
rs117630895 | snp | C/G | 0.00438332 | 0.0466095 | upstream-variant-2KB, intron-variant | UTP18, MBTD1 | GRCh38.p7 | 17:51259743 | AGCAGGCCAGGGAGC[C/G]GGGTCAGGGAGCTGC | 51096 |
rs117654030 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UTP18 | GRCh38.p7 | 17:51267429 | ATGTTGTGCCACCAC[C/T]TCTTCAATCTAGTTC | 51096 |
rs117733211 | snp | C/G | 0.0486741 | 0.148216 | intron-variant | UTP18 | GRCh38.p7 | 17:51270646 | GTTCTTCCAGAGTTG[C/G]CTAAGATGTTGACAT | 51096 |
rs117760862 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | UTP18 | GRCh38.p7 | 17:51275572 | TGACTACATACTAGT[A/G]CTCCAAGAATGAGTA | 51096 |
rs117832768 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51291046 | TAAATCAAGGATGAG[C/T]GAGCTTTTACTTGTT | 51096 |
rs117896554 | snp | C/T | 0.0337553 | 0.125452 | intron-variant | UTP18 | GRCh38.p7 | 17:51267682 | ATGATGTGTACCAGA[C/T]ACTGCCCCTCAAAGT | 51096 |
rs117932582 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | UTP18 | GRCh38.p7 | 17:51277558 | AGACAAGCAATTGCA[A/G]ATACTTGGCTGTAAA | 51096 |
rs117987336 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UTP18 | GRCh38.p7 | 17:51289736 | TACTACCAGATTGTA[C/T]GCACTTTACAAAGTG | 51096 |
rs118005729 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51293165 | ATTAAGCTAGAGTGG[A/G]TACTTTTTGCTTTAG | 51096 |
rs118155832 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | UTP18 | GRCh38.p7 | 17:51267978 | TCTTTGCCCTCTTCC[A/G]GGTACCAGTTGTTGT | 51096 |
rs118159664 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51278623 | GTTTTCACATTTCCA[C/T]CGCCTGATACTGTGC | 51096 |
rs138022579 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51274135 | TTCTTGGACATGCTG[C/G]TAGGTCCTTTCTTGC | 51096 |
rs138069555 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | UTP18 | GRCh38.p7 | 17:51271643 | GATGTACTGTTAAAA[A/C]CATCTATTGGAGGCT | 51096 |
rs138216865 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51285120 | GTTTTCCAGAACTAG[A/G]AGGGTTATAATAGGT | 51096 |
rs138275662 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | UTP18 | GRCh38.p7 | 17:51282938 | CAGTGGCACGATCTC[A/G]GCTCACTGTAACCTC | 51096 |
rs138327944 | snp | C/T | 0.118235 | 0.212457 | intron-variant | UTP18 | GRCh38.p7 | 17:51295157 | TGTAGGTTGCCTGTT[C/T]ACTCTGATGGTAGTT | 51096 |
rs138465436 | in-del | -/AGGA | | | intron-variant | UTP18 | GRCh38.p7 | 17:51282519 | AGATGGAAGGAAGGA[-/AGGA]AGGAAAGAAAGAAAG | 51096 |
rs138558203 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UTP18 | GRCh38.p7 | 17:51265721 | GGTGTGTGCCACCCC[A/G]CCCAGCTAATTTCTG | 51096 |
rs138604315 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UTP18 | GRCh38.p7 | 17:51270987 | TTCATGATTATCTCC[A/G]GTGTGTTATTTTTAT | 51096 |
rs138656063 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UTP18 | GRCh38.p7 | 17:51268114 | TCCCGGGTTCACACC[A/G]TTCTCCTGCCTTAGC | 51096 |
rs138745715 | snp | C/T | 1.65611e-05 | 0.00287755 | synonymous-codon | UTP18 | GRCh38.p7 | 17:51285264 | TGGAGAAGTTTATGT[C/T]TGGGATGTGAACTCA | 51096 |
rs138984854 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51291210 | AAGTTGGATCTTTAT[A/C]GGCATTTTTCCTAAT | 51096 |
rs139058766 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | UTP18 | GRCh38.p7 | 17:51283797 | TTTTTGTATTTTTAG[C/T]AGAGATGGTGATTCA | 51096 |
rs139106379 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51261664 | TAAACGAGTAAACTT[C/G]AGGTTTGTTGGTGAC | 51096 |
rs139380173 | in-del | -/CTT | 0.00676609 | 0.0577691 | intron-variant, cds-indel | UTP18 | GRCh38.p7 | 17:51288839 | AAGTCCGGAGGAAAC[-/CTT]CTAAGAGTCCTCTTC | 51096 |
rs139412834 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | UTP18 | GRCh38.p7 | 17:51268736 | GGAAGAGAGTCCATA[C/T]GTATTCTCAAGGGTG | 51096 |
rs139474786 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51262374 | CAAGTGTGAGCCACC[A/G]CACCCGGCCTAGGTT | 51096 |
rs139488512 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51287780 | TGACTGTGAAGGAAT[A/C]AGGATGCAAGAAGAG | 51096 |
rs139502935 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51295985 | CAGTTTACTCCACTA[C/G]ATTTAATTGATTTCT | 51096 |
rs139567394 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | UTP18 | GRCh38.p7 | 17:51292539 | GGTTTTTACCCAGCA[C/T]TTGCCTGTGAAAATC | 51096 |
rs139685326 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UTP18 | GRCh38.p7 | 17:51271992 | CTTACTTTTAATTAC[A/G]TATTTTTCAGCTCTA | 51096 |
rs139843590 | snp | C/G | 0.0345262 | 0.126772 | intron-variant | UTP18 | GRCh38.p7 | 17:51276820 | GTGGGTGGACAAACT[C/G]AAGAAATTAGTAGGG | 51096 |
rs139916864 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51275438 | GTGGGGACAACTGTG[A/C]AGTGCCTCTTGCATT | 51096 |
rs139983702 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UTP18 | GRCh38.p7 | 17:51272245 | CTGGGATTACAGACA[C/T]AAGCCATCATGCCCA | 51096 |
rs140184058 | snp | C/T | 0.000557362 | 0.0166844 | intron-variant, missense | UTP18 | GRCh38.p7 | 17:51286524 | ATATATCCCTACCAC[C/T]GTTTGCAAATTGGAG | 51096 |
rs140248846 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51279941 | GAAACTCATTTGTCA[A/G]TAGATGATAGTTTTA | 51096 |
rs140283846 | snp | G/T | 0.00914312 | 0.0669923 | intron-variant | UTP18 | GRCh38.p7 | 17:51274071 | CTTAGCCTCATATCA[G/T]ACCTGTTTCCCATGA | 51096 |
rs140463671 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | UTP18 | GRCh38.p7 | 17:51290586 | GGTATACTAGTAATA[C/T]TAACCTTTTATCACT | 51096 |
rs140533967 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UTP18 | GRCh38.p7 | 17:51293252 | GATGCTGTACTGACG[A/C]TTTTTTCTCTTTCTT | 51096 |
rs140673822 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51272941 | TGCTGACATTGATCA[C/T]TCAGCTAAAAGTTCT | 51096 |
rs140814565 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UTP18 | GRCh38.p7 | 17:51281450 | CTCTTTTGTCACTTG[A/G]TTTTCAGGAAACCTT | 51096 |
rs140995070 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51262950 | TCCTGTAATTTCTGT[A/G]GTTCTGACATTTCTC | 51096 |
rs141104008 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51270357 | CCATTTTTTTGGTGG[C/T]GTACTTCTAGACCCT | 51096 |
rs141160865 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UTP18 | GRCh38.p7 | 17:51291658 | AAGAATTGCTTGCCC[C/G]CAAGAGGCGGAGGTT | 51096 |
rs141301868 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime | UTP18 | GRCh38.p7 | 17:51288907 | TAATGAGTTGTAACA[A/G]CATGTGTTAAGTGTT | 51096 |
rs141364350 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UTP18 | GRCh38.p7 | 17:51284699 | GATTTTTTTCCTGTA[A/T]ACCTAAAGGTACTGT | 51096 |
rs141542016 | snp | A/T | 0.0170251 | 0.090679 | intron-variant | UTP18 | GRCh38.p7 | 17:51294933 | TATTGTGGTTTTTAT[A/T]TGCATTTCTCTGATG | 51096 |
rs141716217 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UTP18 | GRCh38.p7 | 17:51270056 | AATCGGGGTTTCACC[A/G]TGTTGGCCAGGCTGG | 51096 |
rs142136736 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UTP18 | GRCh38.p7 | 17:51284395 | TAGCCTTTTTTTTTT[A/G]ATCATTTAAATAACT | 51096 |
rs142177703 | snp | C/T | 0.000798403 | 0.0199641 | downstream-variant-500B | UTP18 | GRCh38.p7 | 17:51298346 | ACCTGGTAGCCTTGT[C/T]CTACAGATTATTAGC | 51096 |
rs142262898 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UTP18 | GRCh38.p7 | 17:51289783 | CTCACTTGGCAAAAA[G/T]CCTTGCATCTGCCAT | 51096 |
rs142315988 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UTP18 | GRCh38.p7 | 17:51285183 | GACTGAGAGTGGCCA[C/G]TTTACTTGCCTTTCA | 51096 |
rs142322446 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | UTP18 | GRCh38.p7 | 17:51269694 | CTATTAGAAAAGACA[A/G]TCTGTTACTAAGTAG | 51096 |
rs142447678 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | UTP18 | GRCh38.p7 | 17:51272533 | ATTTCATTGAGTGGT[A/G]GACATTGCATATGAA | 51096 |
rs142678112 | snp | C/T | | | downstream-variant-500B | UTP18 | GRCh38.p7 | 17:51298361 | CCTACAGATTATTAG[C/T]CACTGCCCTTCCTGG | 51096 |
rs142716887 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51261448 | TTGCCAGATACCCTT[C/T]CTGGCAATGGCAAAC | 51096 |
rs142819417 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | UTP18 | GRCh38.p7 | 17:51262575 | GCTCTTCTTGTTGGT[C/G]ACAGATAAATTACAC | 51096 |
rs142885935 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UTP18 | GRCh38.p7 | 17:51282673 | TACTGAAATTTGATA[C/T]ATGAATTGGACGCAG | 51096 |
rs142907880 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UTP18 | GRCh38.p7 | 17:51290903 | TTATAATGATCTAGA[C/T]GGTTTTGTCATCCCA | 51096 |
rs142974298 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51286245 | GATTCTGAAGATGCA[A/G]GGTGAGAGGATGAGG | 51096 |
rs143167506 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UTP18 | GRCh38.p7 | 17:51274418 | CATATTAACAGATCT[C/T]TCTGTGACATAGATA | 51096 |
rs143209720 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | UTP18 | GRCh38.p7 | 17:51289794 | AAAAGCCTTGCATCT[A/G]CCATCAGCTTTGTAT | 51096 |
rs143306336 | snp | A/G | 0.0170251 | 0.090679 | upstream-variant-2KB, utr-variant-5-prime, intron-variant, nc-transcript-variant | UTP18, MBTD1 | GRCh38.p7 | 17:51259991 | AGACCGGTGGCGGGT[A/G]CAGCAGCCCCCGGAT | 51096 |
rs143342911 | snp | C/T | 0.00597247 | 0.0543191 | upstream-variant-2KB, intron-variant | UTP18, MBTD1 | GRCh38.p7 | 17:51259288 | ACCCTTTTAAATATG[C/T]AGCCTTGGAGGCTGC | 51096 |
rs143448927 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51266979 | GCTGGGACTACAGGC[A/G]TGTACCACCTTAATT | 51096 |
rs143457875 | snp | A/G | 0.0486741 | 0.148216 | intron-variant, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51262297 | CACCATCTTCGCCAG[A/G]CTGGTCTCAAACTCC | 51096 |
rs143500119 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | UTP18 | GRCh38.p7 | 17:51296090 | ATATGCGCTGTCCAG[G/T]TTCTTTTCTGTACCC | 51096 |
rs143657721 | snp | A/G | 1.68664e-05 | 0.00290395 | missense | UTP18 | GRCh38.p7 | 17:51294042 | GCAAGGCCCTGATGT[A/G]TAGGTAGGTATTATT | 51096 |
rs143913231 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | UTP18 | GRCh38.p7 | 17:51275469 | TGTGCCATGAATGCA[A/G]AGATGCCAGGTGCCA | 51096 |
rs144001760 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | UTP18 | GRCh38.p7 | 17:51283842 | TTGGTCTCGAACTCC[G/T]GGCCTCAAGTGAGCC | 51096 |
rs144228652 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | UTP18 | GRCh38.p7 | 17:51269052 | AGTGCTTTGGGAGCC[C/T]GAGGCGGGTGGATCG | 51096 |
rs144482693 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UTP18 | GRCh38.p7 | 17:51283589 | ACCTTTTTCTAACTT[C/T]ACTGGTTTTGTCTTT | 51096 |
rs144551227 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | UTP18 | GRCh38.p7 | 17:51278476 | TTGAGAGAAAGCGCA[C/G]CATGCGTTGGCCAAG | 51096 |
rs144605003 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | UTP18 | GRCh38.p7 | 17:51273049 | TTTTTAAATGAAATG[C/G]TGGCTTTAAACTTTT | 51096 |
rs144638333 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UTP18 | GRCh38.p7 | 17:51270935 | TGACTTGTTGAAGGT[A/G]TACTTATTGTTGACA | 51096 |
rs144856744 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | UTP18 | GRCh38.p7 | 17:51291270 | GGGCTATAAATAGAT[A/G]TCAGAGCACAGCATA | 51096 |
rs144923292 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51284084 | CAGACATATAAGGCA[A/G]AGGTTTTAATATTTG | 51096 |
rs145082102 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UTP18 | GRCh38.p7 | 17:51294445 | CTGAGTGAGAACATG[C/T]GGTGTTTGGTTTTTT | 51096 |
rs145172515 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | UTP18 | GRCh38.p7 | 17:51292601 | GTGGAGGATGACTAA[A/C]TGCCCAGCTGAATGA | 51096 |
rs145235289 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | UTP18 | GRCh38.p7 | 17:51289075 | TTTGTACAAACAGTT[C/T]AGGCACAGTGAGCTA | 51096 |
rs145254803 | snp | A/G | 0.0023933 | 0.0345097 | upstream-variant-2KB, intron-variant | UTP18, MBTD1 | GRCh38.p7 | 17:51258590 | ACACAGGTCAAATAC[A/G]GGTGTGGGCGGTAAT | 51096 |
rs145331910 | snp | A/G | 0.000895038 | 0.0211357 | missense | UTP18 | GRCh38.p7 | 17:51280103 | CATTTGCTAGCAATG[A/G]AGGTAAAGCATTATT | 51096 |
rs145532149 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant, utr-variant-3-prime | UTP18 | GRCh38.p7 | 17:51288809 | AATCAGCAAAGGGAA[A/G]GGGTACATGGAGTAA | 51096 |
rs145640381 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | UTP18 | GRCh38.p7 | 17:51293572 | TGGCCCAAGACAATT[A/C]TTCTTCCGTTGTGGC | 51096 |
rs145840129 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51276916 | CCGTGTGTTCAGCAA[C/G]CCAGAAGCTCTCTGA | 51096 |
rs146039819 | in-del | -/TA | | | intron-variant | UTP18 | GRCh38.p7 | 17:51293541 | ACCTGTCGTTAGTGT[-/TA]GTGTATTTTATGTGT | 51096 |
rs146144536 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51286368 | TTTCTTAGACCAAAC[A/T]CAATTGAGCCATGAA | 51096 |
rs146183479 | in-del | -/CG | | | intron-variant, downstream-variant-500B | UTP18 | GRCh38.p7 | 17:51286982 | CCCTCCCCCTTCCCC[-/CG]CCCCGACCCACAGGC | 51096 |
rs146245990 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | UTP18 | GRCh38.p7 | 17:51271187 | CATAGTACTTTTGAA[C/G]TGGCTTGATGTCTTC | 51096 |
rs146263688 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51268673 | GGTTGGGACTGTTCT[A/G]TGTGAGTAAAGATAA | 51096 |
rs146565564 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51294286 | CATGTGCCATGTTGG[C/T]ATGCTGCACCCATTA | 51096 |
rs146664029 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | UTP18 | GRCh38.p7 | 17:51279307 | TCTCTAAGCATTTTG[A/G]TATCAGGAGGAGTCC | 51096 |
rs146682867 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UTP18 | GRCh38.p7 | 17:51273100 | AGTAACCATCTGTGT[A/G]TGTGTTAGTCTTTCA | 51096 |
rs146937759 | in-del | -/C | 0.0154538 | 0.0865337 | intron-variant | UTP18 | GRCh38.p7 | 17:51296735 | CAGGTATTTCATAGA[-/C]CCCCCCATGTGAAAC | 51096 |
rs147000436 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UTP18 | GRCh38.p7 | 17:51284985 | AAAATCACTTGAACC[C/T]GGGAGAAGGAGGTTG | 51096 |
rs147022889 | snp | G/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51282769 | GCAGGGAAGGAGAAA[G/T]CAAAAGTTGAGCCTT | 51096 |
rs147081134 | in-del | -/TATATTTT | | | intron-variant | UTP18 | GRCh38.p7 | 17:51271575 | GTACTTCAGTCTGGG[-/TATATTTT]TCTGATTCGTTTTCT | 51096 |
rs147110268 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51265420 | AGGCTCCTGCCACCA[C/T]GCTGGACTAATTTTG | 51096 |
rs147126486 | snp | C/T | 0.0123036 | 0.0774623 | upstream-variant-2KB, utr-variant-5-prime | UTP18, MBTD1 | GRCh38.p7 | 17:51260437 | GGAGCGGGAGTTACG[C/T]AGAGGGAGGGAGTGC | 51096 |
rs147175181 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | UTP18 | GRCh38.p7 | 17:51297875 | AATGATTTATAGATC[C/T]AGCTGTGCTTAAGAG | 51096 |
rs147281058 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UTP18 | GRCh38.p7 | 17:51276512 | AGTTATTAGAGCAAA[A/G]CGATAATATAACCTC | 51096 |
rs147349470 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | UTP18 | GRCh38.p7 | 17:51295515 | AGATGGTTGTAGATA[C/T]GCAGCATTATTTCTG | 51096 |
rs147365497 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51292120 | CCTTCCCAAATTAAA[C/T]GTAAATAAATTTTGC | 51096 |
rs147460555 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51275330 | AAAATAAATAACAAA[A/G]TAGTCCAGGTGATGG | 51096 |
rs147476187 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | UTP18 | GRCh38.p7 | 17:51272133 | AGACAGAGTCTTATT[C/T]TGTTGCCCAGGCTGG | 51096 |
rs147613848 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | UTP18 | GRCh38.p7 | 17:51292640 | GTATATATTTGAACA[C/T]GAAGGTGCTATATCT | 51096 |
rs147630211 | snp | G/T | 0.0115144 | 0.0749975 | intron-variant, downstream-variant-500B | UTP18 | GRCh38.p7 | 17:51289236 | AAGTCTCACTCTGTT[G/T]CCCAGGCTGGACTGC | 51096 |
rs147717469 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51272388 | ACAGATGTGAGCCAC[C/T]GCGCCTGGCCTGAAC | 51096 |
rs147912664 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51269826 | CCTCTGCTTAAATAT[A/G]TCAAATAATGTATTG | 51096 |
rs147997292 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | UTP18 | GRCh38.p7 | 17:51267354 | TTTATTGAGGTGAAA[G/T]TCACATAACAGTGTT | 51096 |
rs148278842 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UTP18 | GRCh38.p7 | 17:51275066 | GCTGGGTGTGGTGGC[A/G]CATGTCTGTAATCCC | 51096 |
rs148292902 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | UTP18 | GRCh38.p7 | 17:51290405 | TGGGTGACAGAGTAA[C/G]AGTCTGTCTCAAAAA | 51096 |
rs148366015 | snp | A/G | 0.00993419 | 0.0697739 | upstream-variant-2KB, intron-variant | UTP18, MBTD1 | GRCh38.p7 | 17:51259564 | GCGGGGGCAGGACGC[A/G]GAGAAAAACTTTCTT | 51096 |
rs148588017 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | UTP18 | GRCh38.p7 | 17:51278226 | ACGTGAATCACCTGG[A/G]GGTCTCATTAAGCTG | 51096 |
rs148608355 | snp | A/G | 0.0486741 | 0.148216 | intron-variant | UTP18 | GRCh38.p7 | 17:51291620 | CACACCTGTAATCCC[A/G]GCTACTCAGGAGGCT | 51096 |
rs148658226 | in-del | -/TATATT | 0.029116 | 0.117091 | intron-variant | UTP18 | GRCh38.p7 | 17:51295854 | CACCTGGGGAATATA[-/TATATT]TTTTGGAAAGCACTA | 51096 |
rs148729382 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51269638 | CCTCATGGTACGTAA[A/G]TGCAGGGAGTCCATA | 51096 |
rs148921887 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UTP18 | GRCh38.p7 | 17:51293625 | CACCCCTGTCCACCA[C/T]TGGAGTGATGGTGAC | 51096 |
rs149041590 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51270795 | AGAGGATCCTAGGAA[A/G]TGTAGTTTGGCTTTG | 51096 |
rs149184079 | snp | A/C | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | UTP18, MBTD1 | GRCh38.p7 | 17:51258769 | CTAAGAGAAAACAGG[A/C]ACGAAATTCCCATAT | 51096 |
rs149233502 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | UTP18 | GRCh38.p7 | 17:51295493 | TTTGTCAGGTTTGTC[A/G]AAGATCAGATGGTTG | 51096 |
rs149233994 | in-del | -/C | 0.0821764 | 0.185298 | intron-variant | UTP18 | GRCh38.p7 | 17:51285561 | AATATTACAGTAGTT[-/C]CCCCCCTTATCTGCA | 51096 |
rs149375989 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51285629 | CACAATCTGAAATCT[A/G]TGTAAGATATTTTGA | 51096 |
rs149430580 | snp | A/C | 0.00953873 | 0.0683987 | intron-variant | UTP18 | GRCh38.p7 | 17:51291228 | CATTTTTCCTAATTA[A/C]TAGTTCAATTATACC | 51096 |
rs149498436 | snp | A/C | 0.0209421 | 0.100162 | intron-variant, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51261787 | CACCGAGAATTACCC[A/C]GGCCATGTTTATTAC | 51096 |
rs149741303 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | UTP18 | GRCh38.p7 | 17:51293386 | TGGGAGAGGGGTAGG[A/G]GATGAGAAATTATCT | 51096 |
rs149776076 | snp | A/T | 0.00835141 | 0.0640778 | intron-variant | UTP18 | GRCh38.p7 | 17:51272086 | ATATATTAAACATAG[A/T]TTTTTTTGTTGTTGT | 51096 |
rs149809015 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | UTP18 | GRCh38.p7 | 17:51264533 | ATGCTATGGGGCTCT[A/G]CCAGTTTGCCTTCCC | 51096 |
rs149830134 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51276902 | CCTCCTCAGCACCTC[C/T]GTGTGTTCAGCAACC | 51096 |
rs149972807 | snp | A/G | 0.000713426 | 0.0188734 | missense | UTP18 | GRCh38.p7 | 17:51268887 | CAGAGACTACTAAGC[A/G]GAAAACATCTTCAGA | 51096 |
rs150075173 | in-del | -/GAAG | | | intron-variant | UTP18 | GRCh38.p7 | 17:51282513 | AAGGAAAGATGGAAG[-/GAAG]GAAGGAAGGAAAGAA | 51096 |
rs150141548 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51281578 | GGGTTTAAGGAGGAT[C/T]TGAGGGCAGGAGAGA | 51096 |
rs150194892 | snp | A/G | 0.00419763 | 0.0456201 | missense | UTP18 | GRCh38.p7 | 17:51285256 | GCAGGGGATGGAGAA[A/G]TTTATGTTTGGGATG | 51096 |
rs150282170 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UTP18 | GRCh38.p7 | 17:51270362 | TTTTTGGTGGCGTAC[C/T]TCTAGACCCTAGATC | 51096 |
rs150419820 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | UTP18 | GRCh38.p7 | 17:51290694 | AGTTCTGCATTGTTT[A/G]CTTCAGTGATCATGA | 51096 |
rs150474356 | snp | A/G | 0.0766824 | 0.180169 | intron-variant | UTP18 | GRCh38.p7 | 17:51295117 | CTTTGTCAGATGAGT[A/G]GGTTGCGACAATTTT | 51096 |
rs150507626 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant, downstream-variant-500B | UTP18 | GRCh38.p7 | 17:51287094 | ACTGCGCAGAAATGA[C/T]CTTCACTCAGATTTG | 51096 |
rs150542904 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | UTP18 | GRCh38.p7 | 17:51268078 | GCAGCGGCGTGATCG[C/T]GGCTCACTGCAAGCT | 51096 |
rs150962060 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UTP18 | GRCh38.p7 | 17:51280905 | ACCTAGGACCAGGCG[C/T]GGTAGCTTACGCCTG | 51096 |
rs151195165 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51284522 | TTTTGGTATCTAAAT[C/T]GCTAACCTTGCCTAT | 51096 |
rs151209827 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | UTP18 | GRCh38.p7 | 17:51298419 | TTAATTTGTATTTCA[A/G]GGTTGGCAGCTGGCT | 51096 |
rs180837929 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | UTP18 | GRCh38.p7 | 17:51272484 | TTCCTTGTGGTTTTT[A/G]GTCAAGTTATCTTGT | 51096 |
rs180839850 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | UTP18 | GRCh38.p7 | 17:51281364 | ATTATTCAGGGGTAA[A/T]TCATTCTCCTATGAT | 51096 |
rs180871589 | snp | A/C/G | 0.00119737 | 0.0244387 | intron-variant | UTP18 | GRCh38.p7 | 17:51290289 | GGCATTGTGGTGGGC[A/C/G]TCTGTAATCCCAGCT | 51096 |
rs180876663 | snp | C/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51265220 | GTTAACAGAGAGAGA[C/G]AAATGTTTATCTATA | 51096 |
rs181110527 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UTP18 | GRCh38.p7 | 17:51268271 | GACCTCGTGATCCGC[A/C]CGCCTTGGCCTCCCA | 51096 |
rs181118428 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UTP18 | GRCh38.p7 | 17:51285829 | AGTTTGAGGCATCCA[C/G]TGGGGGTCTTGGAAC | 51096 |
rs181141684 | snp | C/G | 0.00279162 | 0.0372561 | upstream-variant-2KB, utr-variant-5-prime, intron-variant, nc-transcript-variant | UTP18, MBTD1 | GRCh38.p7 | 17:51259977 | CCCCGGCTGGGCCCA[C/G]ACCGGTGGCGGGTGC | 51096 |
rs181154558 | snp | A/G | 1.67337e-05 | 0.00289251 | missense | UTP18 | GRCh38.p7 | 17:51275866 | TTTCATTTCCTATAG[A/G]TGAAGAACTGCCAGC | 51096 |
rs181161572 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51296746 | ATAGACCCCCCATGT[A/G]AAACTTTGGAGTAAG | 51096 |
rs181306536 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51264364 | TTTTTCCCTTTAATG[C/G/T]AGATTATTTCAGCAT | 51096 |
rs181312719 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UTP18 | GRCh38.p7 | 17:51279454 | GAGAAGCTAGTCAGT[C/T]CTTAAGTAAACTGAC | 51096 |
rs181394444 | snp | A/C/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51292083 | AAGCCAAGGTACTTA[A/C/T]CACAAATTTATATAA | 51096 |
rs181510163 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UTP18 | GRCh38.p7 | 17:51272688 | TTCAGTTTTGGGAAG[A/T]TTTTCTTATAATTCT | 51096 |
rs181544979 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51261363 | TGTCCCCATGTGACT[A/G]TGAGACCCACCATGT | 51096 |
rs181550518 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51276308 | ACATTTTTATTGAAT[A/G]CACCTGTATGACTTC | 51096 |
rs181553332 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | UTP18 | GRCh38.p7 | 17:51297076 | AGTTGGTGGAAGCAG[C/T]ACATTAGCTGAGCTT | 51096 |
rs181763122 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | UTP18 | GRCh38.p7 | 17:51293440 | TTGTCCAACCCACGG[C/T]GCAGGACGGTTTGAT | 51096 |
rs181976894 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51279702 | TAGAGGTATTACTGC[A/T]TATATTTGGAAAATT | 51096 |
rs182003009 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51285000 | CGGGAGAAGGAGGTT[A/G]CAGTGTGCTGAGATG | 51096 |
rs182038881 | snp | G/T | 0.0146672 | 0.084371 | intron-variant | UTP18 | GRCh38.p7 | 17:51268021 | TGTTTTTTGTTTTTT[G/T]TTTTTTGAGATGGAG | 51096 |
rs182155212 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UTP18 | GRCh38.p7 | 17:51282817 | TTTGAAATGTTGATG[A/G]TTCTCTTCCTCTCTC | 51096 |
rs182190024 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime | UTP18 | GRCh38.p7 | 17:51297797 | GTCCAGTTGAGTCAC[A/C]AGAGAAGCCTGTCTT | 51096 |
rs182229868 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51261667 | ACGAGTAAACTTCAG[A/G]TTTGTTGGTGACAAG | 51096 |
rs182343319 | snp | C/T | 0.000752664 | 0.0193847 | synonymous-codon | UTP18 | GRCh38.p7 | 17:51288197 | AATGAAAGAAGCAGT[C/T]AGATTGGTAAATATT | 51096 |
rs182506459 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51276385 | CTTCCACTGAATATA[A/G]AAGTTCAGTAAAATA | 51096 |
rs182531477 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51262282 | GTAGAAACGGGGTTT[C/T]ACCATCTTCGCCAGG | 51096 |
rs182544831 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UTP18 | GRCh38.p7 | 17:51274022 | CCTTATCGTATTCTA[C/T]ACTGCCCTTTACAGT | 51096 |
rs182744370 | snp | A/G | 0.0232847 | 0.105357 | intron-variant | UTP18 | GRCh38.p7 | 17:51265553 | CAGGCATGAGCCACC[A/G]TGCCCGGCCTTTTTT | 51096 |
rs182751651 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51281724 | AAATGTTAACATTGG[C/G/T]GGGGAACTGGTAAAG | 51096 |
rs182763160 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | UTP18 | GRCh38.p7 | 17:51293764 | TGGAACACTTTGCTG[A/C]ACTAATAGACTGTAC | 51096 |
rs182775949 | snp | A/G | 0.000153478 | 0.00875872 | intron-variant | UTP18 | GRCh38.p7 | 17:51277083 | ATACTACCAGGATAC[A/G]GGGTCTGTGGAAATA | 51096 |
rs182975282 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UTP18 | GRCh38.p7 | 17:51277649 | TTCTTTGGACAAACT[C/G]TTTCACCTCTCTGAT | 51096 |
rs183017777 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UTP18 | GRCh38.p7 | 17:51263072 | TGTTCCATCTTGCCT[C/T]ACCTGTCCAGTCGGT | 51096 |
rs183061514 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UTP18 | GRCh38.p7 | 17:51294155 | AATTCTAGTCTGTTT[A/G]TCTTGACTCTCATCT | 51096 |
rs183078228 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51270794 | GAGAGGATCCTAGGA[A/G]GTGTAGTTTGGCTTT | 51096 |
rs183095451 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | UTP18 | GRCh38.p7 | 17:51272958 | CAGCTAAAAGTTCTG[G/T]TTTTTATTCATGTGA | 51096 |
rs183316734 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51274534 | GCAACCTCCGCCTCC[C/T]GGGTTCAAGCAATTC | 51096 |
rs183361015 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51269633 | TTAGTCCTCATGGTA[C/T]GTAAATGCAGGGAGT | 51096 |
rs183383425 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UTP18 | GRCh38.p7 | 17:51269227 | GGGAAGACTAGGGTG[C/T]AATAACCTGTGATAA | 51096 |
rs183577001 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | UTP18 | GRCh38.p7 | 17:51266975 | CATAGCTGGGACTAC[A/G]GGCATGTACCACCTT | 51096 |
rs183633083 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51285979 | TCACATCAAGTTTTC[C/G]TATAATTATTTTCAG | 51096 |
rs183651916 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51282600 | TGGTAGAGAGAGAGT[C/T]GGGGAGGGAGAAGAG | 51096 |
rs183790359 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | UTP18 | GRCh38.p7 | 17:51263738 | CACAATGATAGTAAC[G/T]ACATCAGAATTTTGT | 51096 |
rs183796206 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51278957 | GTCTTTGGGAGACAG[A/G]ACTAGAGTGGGATGT | 51096 |
rs183862413 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UTP18 | GRCh38.p7 | 17:51266515 | GTGATAATATTGCTT[A/G]CTTGTTCATTTGCAT | 51096 |
rs184016270 | snp | C/G | | | upstream-variant-2KB, utr-variant-5-prime, intron-variant, nc-transcript-variant | UTP18, MBTD1 | GRCh38.p7 | 17:51260051 | ATATCAACAACATTA[C/G]CATAGCCCTCCCTCC | 51096 |
rs184023650 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51276100 | ATATTCATAGCTAAA[A/G]CATCATAGCCCGAAG | 51096 |
rs184058846 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | UTP18 | GRCh38.p7 | 17:51283739 | ATGCCTCAGCCTCCC[A/C]GAGTAGCTGGGATTA | 51096 |
rs184225441 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | UTP18 | GRCh38.p7 | 17:51275728 | TGTTTTTTGTTTTTT[G/T]TTTTTGAGTTGTGTT | 51096 |
rs184263787 | snp | A/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51264579 | TTTCAGTCCATTCTT[A/T]GACACAATGGTTTAT | 51096 |
rs184268745 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | UTP18 | GRCh38.p7 | 17:51279520 | TGTTTTTGTTTTTGA[C/G]TCACAAAGTTAAAGA | 51096 |
rs184358559 | snp | A/G | 0.00318978 | 0.0398085 | upstream-variant-2KB, intron-variant | UTP18, MBTD1 | GRCh38.p7 | 17:51259659 | GGTGGGGGGAGGGGA[A/G]CCCCTGAATCGTTTA | 51096 |
rs184380703 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51296473 | CAGGATAATTTCATC[A/G]GTCTCATTTCAGATC | 51096 |
rs184708681 | snp | C/G | 0 | 0 | intron-variant | UTP18 | GRCh38.p7 | 17:51275591 | CAAGAATGAGTAATA[C/G]ATTCAGACTTCTAGA | 51096 |
rs184714612 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51295115 | CCCTTTGTCAGATGA[A/G]TAGGTTGCGACAATT | 51096 |
rs184738538 | snp | G/T | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | UTP18, MBTD1 | GRCh38.p7 | 17:51258662 | CAGTTTTAGACATCC[G/T]TAGAAGTGATTTAGG | 51096 |
rs184824188 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | UTP18 | GRCh38.p7 | 17:51296748 | AGACCCCCCATGTGA[A/C]ACTTTGGAGTAAGCC | 51096 |
rs184837624 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UTP18 | GRCh38.p7 | 17:51267221 | GCCCTTCTTGGCCTC[A/G]CAAAGTGCTGGGAAT | 51096 |
rs184939799 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UTP18 | GRCh38.p7 | 17:51272160 | CTGGAGTGCAGTGGC[A/G]CAATCTCAGCTCACT | 51096 |
rs184949524 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | UTP18 | GRCh38.p7 | 17:51289622 | AATCTTCAGGCAGAG[C/G]CAATTTTCTCATTCA | 51096 |
rs184968621 | snp | C/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51295534 | GCATTATTTCTGAGG[C/G]CTCTGTTCTGTTCCA | 51096 |
rs185118024 | snp | A/T | 0.00795532 | 0.062565 | intron-variant | UTP18 | GRCh38.p7 | 17:51271485 | CTAATGAAAAAAAAA[A/T]TTTTTTTTTGTAGTG | 51096 |
rs185191501 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, missense | UTP18 | GRCh38.p7 | 17:51288567 | GTTGTCTTAACAGAA[C/T]GGAGGCAATTCTCGG | 51096 |
rs185192993 | snp | A/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51268031 | TTTTTTTTTTTTGAG[A/T]TGGAGCCTGGCTCTG | 51096 |
rs185199802 | snp | A/T | 1.65608e-05 | 0.00287752 | missense | UTP18 | GRCh38.p7 | 17:51285270 | AGTTTATGTTTGGGA[A/T]GTGAACTCAAGGAAG | 51096 |
rs185322090 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51284364 | AACTATTTGTGCTTA[C/T]TCGTAAGCTTGTGTT | 51096 |
rs185443460 | snp | A/C | | | intron-variant | UTP18 | GRCh38.p7 | 17:51281467 | TTTCAGGAAACCTTC[A/C]GGGGGCAAAGGAAAA | 51096 |
rs185482583 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51267516 | AAAGAAAACTCTCCA[G/T]TAATTAGTCACTTTG | 51096 |
rs185483159 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51265407 | TAGATGGGATTACAG[A/G]CTCCTGCCACCACGC | 51096 |
rs185609294 | snp | A/C/G | 1.65773e-05 | 0.00287895 | intron-variant | UTP18 | GRCh38.p7 | 17:51263270 | GGTGTTTTGTCTGCT[A/C/G]TAGGTTCAAGAACAT | 51096 |
rs185748295 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UTP18 | GRCh38.p7 | 17:51278091 | GCCAACTTTAGAAAC[A/G]TTTATGATGTTTATC | 51096 |
rs185854002 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UTP18 | GRCh38.p7 | 17:51276632 | TTCACTTCAGGATGT[C/T]ACTCTCTGATGGGGG | 51096 |
rs185972745 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51261837 | ATGTCAGCTGCTTAC[C/T]AGAGCCGCCTTCGGG | 51096 |
rs185985585 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UTP18 | GRCh38.p7 | 17:51297212 | ACAGCAATCTGGCTC[A/G]GTTCTTCTGAGGTCT | 51096 |
rs186023834 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51261455 | ATACCCTTTCTGGCA[A/G]TGGCAAACCCTGCGT | 51096 |
rs186032054 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51276309 | CATTTTTATTGAATG[C/T]ACCTGTATGACTTCA | 51096 |
rs186119223 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | UTP18 | GRCh38.p7 | 17:51290918 | CGGTTTTGTCATCCC[A/G]TTACAAAGCACTGTG | 51096 |
rs186232605 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UTP18 | GRCh38.p7 | 17:51293468 | GATTGTGGCCCAACA[C/T]TAATTTGTAAACTTT | 51096 |
rs186242424 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | UTP18 | GRCh38.p7 | 17:51272589 | GGATGATGGTTTATA[C/T]GTTTACTTCTAGGTA | 51096 |
rs186274344 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UTP18 | GRCh38.p7 | 17:51273735 | CGAGACCCTGTCTCT[A/C]AAATAATAAATAAAT | 51096 |
rs186351982 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UTP18 | GRCh38.p7 | 17:51268528 | CTTCTTTACATAGTC[C/T]TGATATCTGGGATGT | 51096 |
rs186541611 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51269949 | CAACCTCTGCCTCCC[A/G]GGTTCCAGTGATTGT | 51096 |
rs186550282 | snp | A/G | | | intron-variant, downstream-variant-500B | UTP18 | GRCh38.p7 | 17:51287009 | AGGCCCCGGTATGTG[A/G]TGTTCCCCTTCCTGT | 51096 |
rs186568432 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51285891 | TAATTGCAGTTGAAC[A/G]CCTTTTTAGCAAAGA | 51096 |
rs186636117 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | UTP18 | GRCh38.p7 | 17:51272814 | TTCCCTTCTTAGCTC[C/T]GCAAGTGTTTTAAGT | 51096 |
rs186750281 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51267141 | CTAATTTTTGTATTT[G/T]TTTGTAGAGATGAGG | 51096 |
rs186761734 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51283478 | TGCACCCTTTTCTTA[C/T]TCTGTATGGAGTCGT | 51096 |
rs186863434 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51292394 | TTCTGGCAAAGTTGA[A/G]AATAATTGAATGTGG | 51096 |
rs186921471 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51286303 | CTACCTTACTAAACC[A/G]CTAATTAGAACCCAT | 51096 |
rs187112433 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | UTP18 | GRCh38.p7 | 17:51269229 | GAAGACTAGGGTGCA[A/G]TAACCTGTGATAAGT | 51096 |
rs187135670 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51277307 | CATCAAGTGAGAGGT[A/T]AGATTTCTGTTGAAT | 51096 |
rs187192613 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51262301 | ATCTTCGCCAGGCTG[G/T]TCTCAAACTCCTGAC | 51096 |
rs187219095 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UTP18 | GRCh38.p7 | 17:51265012 | TATTCTTTATTATGT[C/T]CTTGTCTATTGGAGA | 51096 |
rs187375421 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UTP18 | GRCh38.p7 | 17:51274919 | TAGTTACCACATGGC[C/T]GGGCGCAGTGGCTCA | 51096 |
rs187386651 | snp | C/G | 6.93878e-05 | 0.00588974 | missense | UTP18 | GRCh38.p7 | 17:51280030 | GAAGATAGTGAGGAG[C/G]TTTGAAGTCTCCCCA | 51096 |
rs187401830 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51281933 | CCTTGTAGCAATACT[C/T]TCTTGACTTTGATGG | 51096 |
rs187403987 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UTP18, MBTD1 | GRCh38.p7 | 17:51258554 | AGAGAGGCCCTTGGA[A/G]GAAAGACTAGCTTCC | 51096 |
rs187460925 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UTP18 | GRCh38.p7 | 17:51278394 | AATATTTAGTAGTTA[C/T]TATTTTTACATGTCA | 51096 |
rs187608185 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | UTP18 | GRCh38.p7 | 17:51277842 | CTCTACCATACCCAT[G/T]CTTTTCCTATATTTC | 51096 |
rs187683485 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51293793 | ACTTTCTTGTGTGCT[A/C]CAATCAAAATGAGCT | 51096 |
rs187705672 | snp | G/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51263720 | TTTCCTTTGTGAAAT[G/T]GGCACAATGATAGTA | 51096 |
rs187852538 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UTP18 | GRCh38.p7 | 17:51275604 | TACATTCAGACTTCT[A/G]GATATGGAAAGCACT | 51096 |
rs187860544 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UTP18 | GRCh38.p7 | 17:51295128 | GAGTAGGTTGCGACA[A/G]TTTTCTCCCATTTTG | 51096 |
rs187976413 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UTP18 | GRCh38.p7 | 17:51271258 | TCTGTTCCAGTCTTC[C/T]TTTCTAGATTATTAG | 51096 |
rs188011740 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UTP18 | GRCh38.p7 | 17:51274285 | GGTCTACACTATTCA[C/G]TTTCTAACTCATCAC | 51096 |
rs188095192 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UTP18 | GRCh38.p7 | 17:51272284 | TTGTATTTTTAGTAG[A/C]GACGGGGTTTCTCCA | 51096 |
rs188103104 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51289867 | AAGTTTGAGCCAAGT[A/C]ACAGTTCTTCAGAGG | 51096 |
rs188217433 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51288322 | GGCTTCTTTTGATAT[A/G]GGAATTATTAGTATT | 51096 |
rs188335306 | snp | C/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51268048 | GGAGCCTGGCTCTGT[C/T]GCCCAGGCTGGAGTG | 51096 |
rs188345480 | snp | C/G | 3.3134e-05 | 0.00407012 | missense | UTP18 | GRCh38.p7 | 17:51285358 | AGGAATGGACAGTAT[C/G]TTGCTTGTGGGTAAG | 51096 |
rs188478953 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51263087 | CACCTGTCCAGTCGG[C/T]GCCATTCTCTGATTT | 51096 |
rs188497486 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UTP18 | GRCh38.p7 | 17:51294305 | CTGCACCCATTAACT[C/T]GTCATTTAGCATTAG | 51096 |
rs188508585 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51264092 | CCTAGGCTGGAGTGC[A/G]GTGGTGCGATCTTGG | 51096 |
rs188511869 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UTP18 | GRCh38.p7 | 17:51266048 | GAACAGAGAAGATGC[A/G]TTTGAAATGTTCACA | 51096 |
rs188514538 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51279136 | ACTAGGCAATATATT[C/T]ACACGGTGTTAAAAA | 51096 |
rs188758967 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UTP18 | GRCh38.p7 | 17:51266516 | TGATAATATTGCTTA[C/T]TTGTTCATTTGCATA | 51096 |
rs188759405 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51276171 | GGAAATACAAAACAG[A/C]ACATCCAGTCAGCAT | 51096 |
rs188767705 | snp | C/T | 0.000199867 | 0.00999467 | intron-variant | UTP18 | GRCh38.p7 | 17:51296949 | TGTTCAGATGACTTA[C/T]TTTTTACTTTTCCAG | 51096 |
rs189047761 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UTP18 | GRCh38.p7 | 17:51282799 | TGGTAAGTTAGGGGT[A/G]ATTTTGAAATGTTGA | 51096 |
rs189193049 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UTP18 | GRCh38.p7 | 17:51271918 | AGTGATCCACTTGCC[C/T]CGGCCTCCCAAAGTA | 51096 |
rs189247757 | snp | C/T | 0.0023933 | 0.0345097 | upstream-variant-2KB, intron-variant | UTP18, MBTD1 | GRCh38.p7 | 17:51259758 | GGGGTCAGGGAGCTG[C/T]GGGGTTCCTGGGGTC | 51096 |
rs189267363 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UTP18 | GRCh38.p7 | 17:51296577 | TCCAAATCCTTTGGT[A/G]TTTTTATAAGTGAAA | 51096 |
rs189466567 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UTP18, MBTD1 | GRCh38.p7 | 17:51258996 | TGAGAAGTAAAAAAA[A/G]GAGCAACTTAACCAG | 51096 |
rs189502115 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | UTP18 | GRCh38.p7 | 17:51272601 | ATATGTTTACTTCTA[G/T]GTAGGTAGCTTGGCA | 51096 |
rs189542925 | snp | A/G | 0.000454752 | 0.0150721 | intron-variant | UTP18 | GRCh38.p7 | 17:51275818 | ACTCTAAAGAAAATA[A/G]TGTTTATTCATTTCA | 51096 |
rs189789525 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | UTP18 | GRCh38.p7 | 17:51291343 | AATGCATTGAGAGAT[G/T]ACACTGGGGAATTTT | 51096 |
rs189794586 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51284147 | ACTGCTTAACCTGCA[C/T]GCTTACTCTAGCCTG | 51096 |
rs190072045 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | UTP18 | GRCh38.p7 | 17:51289265 | GCAGTGGTGTGATCT[C/T]GGCTCACTGCAGCCT | 51096 |
rs190076421 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | UTP18 | GRCh38.p7 | 17:51264713 | TTTTTTTGAGACTCT[C/G]ATCCTTTCATCCAGG | 51096 |
rs190086469 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UTP18 | GRCh38.p7 | 17:51267384 | TAGGCATTTTAAAGT[A/G]TAAATTTGGTGGCAT | 51096 |
rs190155890 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UTP18 | GRCh38.p7 | 17:51281473 | GAAACCTTCAGGGGG[C/T]AAAGGAAAAACTTCC | 51096 |
rs190193422 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UTP18 | GRCh38.p7 | 17:51265548 | GATTGCAGGCATGAG[C/T]CACCGTGCCCGGCCT | 51096 |
rs190334735 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UTP18 | GRCh38.p7 | 17:51279550 | ATGAGATTCCTGTCC[A/G]TCATGAGCTGCTTAG | 51096 |
rs190355348 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | UTP18 | GRCh38.p7 | 17:51267707 | CAAAGTCCAGTTGTA[G/T]CAGTCTCTTTCAAGT | 51096 |
rs190398967 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UTP18 | GRCh38.p7 | 17:51277492 | AGTGAACTTTTTTAC[C/T]GAACACTTACGGAAT | 51096 |
rs190442631 | snp | C/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51262843 | AGGCATGAGGCATTG[C/T]GCTCTCTGCTGGTAT | 51096 |
rs190564294 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51272913 | GCTCTTTTTGAAGTT[C/T]TGATACATAGATTGC | 51096 |
rs190567294 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51284986 | AAATCACTTGAACCC[A/G]GGAGAAGGAGGTTGC | 51096 |
rs190570620 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UTP18 | GRCh38.p7 | 17:51292951 | GGCAAAGTGTATATA[C/T]AATAGTTGAAAATTA | 51096 |
rs190803501 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51269533 | CTCTCACATCATGTG[A/G]GAGCTCCTTCCTTAG | 51096 |
rs190837883 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51297625 | GATTTAATTAGGACA[A/G]AGGATTTTTAAAGGT | 51096 |
rs190839633 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51276346 | AAGGAACCATAATAA[C/T]AGGGGATTTGGAGTA | 51096 |
rs190846467 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51262054 | GTTTTGGGAAGCTCA[A/C]ACTCACTTCAAGGGA | 51096 |
rs190857152 | snp | C/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51265013 | ATTCTTTATTATGTC[C/T]TTGTCTATTGGAGAC | 51096 |
rs191037980 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51293649 | TGGTGACACTTAAGA[A/G]CCCAGACTTCACCAC | 51096 |
rs191053497 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UTP18 | GRCh38.p7 | 17:51277050 | TATTTTTAAATGAAC[A/G]CTTGTAGTGAAAAGT | 51096 |
rs191077969 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51273879 | TATTGCAGTAGCTTT[A/G]TGACTGGACTCTTTA | 51096 |
rs191307031 | snp | A/G | 0.00268967 | 0.0365732 | missense | UTP18 | GRCh38.p7 | 17:51293933 | TGTACAGTATTTTCA[A/G]ACTTCCCAGTCATTA | 51096 |
rs191322537 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UTP18 | GRCh38.p7 | 17:51270482 | AATTTTGGGTATGGT[A/T]ATGCTAGCTGTTGAA | 51096 |
rs191328921 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51287606 | TATGCATGTGGCCAC[C/G]CCCACAAACCTTTAG | 51096 |
rs191371876 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UTP18 | GRCh38.p7 | 17:51285903 | AACACCTTTTTAGCA[A/G]AGAAAATGCTGGCGC | 51096 |
rs191567313 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UTP18 | GRCh38.p7 | 17:51267175 | TTCGCCATGTCGCCC[A/G]GGCTGGTCTTGAACT | 51096 |
rs191576480 | snp | C/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51283689 | TGTGATCTTGGCTCA[C/G]TACATCCTCTGCCTC | 51096 |
rs191607691 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51269164 | TGGTGGTATGTTCCT[A/G]TAGTCCCGACTACTT | 51096 |
rs191610826 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | UTP18 | GRCh38.p7 | 17:51266388 | TGAAACAGTAAGAGG[A/T]TTGCTATTGTGGGCA | 51096 |
rs191913860 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51282369 | GACTTTCACAAGGTT[A/G]TTTACATTGGTATGT | 51096 |
rs192113827 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UTP18 | GRCh38.p7 | 17:51280623 | GGTAAGATCAGCCTG[A/G]CCAACATGGTAAAAC | 51096 |
rs192159695 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | UTP18 | GRCh38.p7 | 17:51274969 | TTGGGAGGCCGAGGC[A/G]GGCAGATCACCTGAG | 51096 |
rs192167608 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UTP18 | GRCh38.p7 | 17:51294387 | CTGGAGTGTCATGTT[C/T]TCCTTCCTGTGTCCA | 51096 |
rs192201945 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UTP18, MBTD1 | GRCh38.p7 | 17:51258621 | CATCTAATCATCCCT[C/T]TACCAGGTGATGCTT | 51096 |
rs192206088 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, missense | UTP18 | GRCh38.p7 | 17:51286686 | ACCCGTGCCAACCCT[A/G]TAGCGAGGGACATCT | 51096 |
rs192219957 | snp | C/T | | | intron-variant, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51261500 | TTTGCACACATTTTG[C/T]TATCCCTTTAAATTC | 51096 |
rs192328942 | snp | G/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51263721 | TTCCTTTGTGAAATG[G/T]GCACAATGATAGTAA | 51096 |
rs192397715 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | UTP18 | GRCh38.p7 | 17:51271991 | GCTTACTTTTAATTA[C/T]GTATTTTTCAGCTCT | 51096 |
rs192404064 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | UTP18 | GRCh38.p7 | 17:51289555 | TGTAAACTCTTTTCT[G/T]CCCAACATCAGAGCT | 51096 |
rs192627241 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51296048 | AGCTGTAAATAAGGG[C/T]GTTAACCACAAAGAT | 51096 |
rs192646028 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | UTP18 | GRCh38.p7 | 17:51274406 | TTAAATATCTGTCAT[A/G]TTAACAGATCTCTCT | 51096 |
rs192658139 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | UTP18 | GRCh38.p7 | 17:51266927 | GGAGTGGTGCTGTCA[G/T]GGCTCATTGCAACCT | 51096 |
rs192720172 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UTP18 | GRCh38.p7 | 17:51278921 | GGGGAGCATGAGTCC[A/T]AGCAAGGGAACTAAG | 51096 |
rs192769796 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51288534 | AATTTTCTTTCCTCA[C/T]TTACCTTTTTAAGGC | 51096 |
rs192911384 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51267422 | ATTTAGAATGTTGTG[C/T]CACCACCTCTTCAAT | 51096 |
rs192996603 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | UTP18 | GRCh38.p7 | 17:51271427 | TCCTCCCACCTCAGC[C/G]TCTGGAGTAGCTAGG | 51096 |
rs193044693 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51277886 | ATCCCAAAATACACC[A/G]ACACCTTCATGCATC | 51096 |
rs193122273 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51284241 | GTACATATGGAAGGG[G/T]GAACTTTAGAGCAAT | 51096 |
rs193143298 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UTP18 | GRCh38.p7 | 17:51282810 | GGGTAATTTTGAAAT[A/G]TTGATGGTTCTCTTC | 51096 |
rs193144842 | snp | A/G | 0.0154538 | 0.0865337 | upstream-variant-2KB, intron-variant | UTP18, MBTD1 | GRCh38.p7 | 17:51259258 | GCAATGGTCACAGAA[A/G]TCCACCGACTTGAAA | 51096 |
rs193222955 | snp | A/G | 0.00416185 | 0.0454269 | intron-variant | UTP18 | GRCh38.p7 | 17:51263236 | GCAGTCATGGGATAG[A/G]AAAATCTCAGTGCTT | 51096 |
rs193286600 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | UTP18 | GRCh38.p7 | 17:51275726 | TTTGTTTTTTGTTTT[G/T]TTTTTTTGAGTTGTG | 51096 |
rs199498899 | snp | A/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51273182 | TTTTTCTTCTCCTTT[A/T]AAATTTTTTTTTTTT | 51096 |
rs199553488 | snp | A/G | 1.77423e-05 | 0.00297839 | missense | UTP18 | GRCh38.p7 | 17:51288051 | TGTGGAGTGGTAAAT[A/G]TATACAATCAAGATT | 51096 |
rs199622153 | snp | C/T | 8.60711e-05 | 0.00655958 | intron-variant | UTP18 | GRCh38.p7 | 17:51280489 | CTTCGGGTAAGACAA[C/T]GACATGAAAGAAGCT | 51096 |
rs199634901 | in-del | -/ATAT | | | intron-variant | UTP18 | GRCh38.p7 | 17:51295849 | AACTTCACCTGGGGA[-/ATAT]ATATATTTTTTGGAA | 51096 |
rs199652773 | snp | C/T | 0.000220296 | 0.0104928 | intron-variant | UTP18 | GRCh38.p7 | 17:51273315 | GGTAGGTAAAAGGGG[C/T]AGCTCATTGATTCTA | 51096 |
rs199741654 | snp | A/G | 0.000606913 | 0.0174094 | synonymous-codon, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51260599 | GATGCCGCCGGAGCG[A/G]AGGAGACGAATGAAA | 51096 |
rs199741655 | in-del | -/T | 0.487177 | 0.0790385 | intron-variant | UTP18 | GRCh38.p7 | 17:51267461 | GGTTTTTTTTTTTTT[-/T]GGTTCTTAAACATTT | 51096 |
rs199759736 | in-del | -/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51293516 | GTTTTTTTTTTTTTT[-/T]AAGCTCATCACCTGT | 51096 |
rs199818161 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UTP18 | GRCh38.p7 | 17:51282524 | GAAGGAAGGAAGGAA[A/G]GAAAGAAAGAAAGAA | 51096 |
rs199848755 | in-del | -/T | | | intron-variant, downstream-variant-500B | UTP18 | GRCh38.p7 | 17:51286822 | ACTCATTATAAGTAG[-/T]TTTTTAAATTTTTTT | 51096 |
rs199856341 | snp | A/G | 0.000182909 | 0.00956143 | missense | UTP18 | GRCh38.p7 | 17:51280097 | TATTTGCATTTGCTA[A/G]CAATGAAGGTAAAGC | 51096 |
rs199888784 | snp | G/T | | | missense | UTP18 | GRCh38.p7 | 17:51277269 | ATGTCTATGACATGC[G/T]GGCTGGAAAGTTAAT | 51096 |
rs199953240 | snp | A/G | 3.31774e-05 | 0.00407279 | synonymous-codon | UTP18 | GRCh38.p7 | 17:51277297 | AATTCCTGTGCATCA[A/G]GTGAGAGGTAAGATT | 51096 |
rs199983161 | snp | A/G/T | 0.000431539 | 0.0146829 | missense | UTP18 | GRCh38.p7 | 17:51273377 | ATGAAAGTGAAGAGG[A/G/T]TGAAGATGATTTGTT | 51096 |
rs200041216 | snp | C/T | 1.67486e-05 | 0.00289379 | missense | UTP18 | GRCh38.p7 | 17:51293927 | CCTTCCTGTACAGTA[C/T]TTTCAAACTTCCCAG | 51096 |
rs200068073 | snp | G/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51267461 | AAAACTTTTTTTTTG[G/T]TTTTTTTTTTTTTGG | 51096 |
rs200193586 | snp | A/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51273738 | GACCCTGTCTCTAAA[A/T]TAATAAATAAATAAA | 51096 |
rs200197807 | snp | G/T | | | intron-variant, downstream-variant-500B | UTP18 | GRCh38.p7 | 17:51289202 | TTCTGTTTTTTTTGT[G/T]TTTTTTTTTTTTGAG | 51096 |
rs200213431 | snp | C/T | 0.000174566 | 0.0093409 | utr-variant-5-prime, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51260580 | GTTTCTCCTCAAACC[C/T]AACGATGCCGCCGGA | 51096 |
rs200396673 | in-del | -/TC | | | intron-variant | UTP18 | GRCh38.p7 | 17:51264607 | TATTTGTTTTTTTTT[-/TC]CAGACTCTGTCAGTT | 51096 |
rs200527501 | snp | A/C | 0.203267 | 0.245593 | downstream-variant-500B | UTP18 | GRCh38.p7 | 17:51297966 | TCCCTCCACCCCCAA[A/C]ACACACACACACAAA | 51096 |
rs200567397 | snp | C/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51287987 | GTTGTGAAAGCCCTT[C/T]TACTTGGTTTTTAAT | 51096 |
rs200630967 | snp | C/T | 1.75943e-05 | 0.00296595 | missense | UTP18 | GRCh38.p7 | 17:51280077 | TCATAAATGGCATTG[C/T]TGGATATTTGCATTT | 51096 |
rs200641862 | snp | A/G/T | 0.000181919 | 0.00953565 | missense, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51260618 | AGACGAATGAAACTG[A/G/T]ACCGGAGAACCGGAG | 51096 |
rs200649417 | snp | C/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51282882 | CTTTTTTTTTTTTTT[C/T]TTTTGAGACAGAGTC | 51096 |
rs200652448 | snp | A/T | 0.0275645 | 0.114116 | intron-variant | UTP18 | GRCh38.p7 | 17:51273739 | ACCCTGTCTCTAAAA[A/T]AATAAATAAATAAAT | 51096 |
rs200723298 | snp | A/G | 0.00163825 | 0.0285734 | missense | UTP18 | GRCh38.p7 | 17:51266199 | TTGACATGATGAACA[A/G]TCGGTTTCGGAAGGA | 51096 |
rs200743453 | snp | C/T | | | synonymous-codon | UTP18 | GRCh38.p7 | 17:51277288 | TGGAAAGTTAATTCC[C/T]GTGCATCAAGTGAGA | 51096 |
rs200766645 | snp | C/T | 1.68148e-05 | 0.0028995 | synonymous-codon | UTP18 | GRCh38.p7 | 17:51293917 | GGTTCATCTTCCTTC[C/T]TGTACAGTATTTTCA | 51096 |
rs200776581 | snp | A/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51273186 | TCTTCTCCTTTAAAA[A/T]TTTTTTTTTTTTTTT | 51096 |
rs200917778 | in-del | -/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51279490 | TGAAAAGTTTTGGGG[-/T]TTTTTTTTGTTTTTT | 51096 |
rs201005625 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51279632 | AGTGGCAGTGTATTT[A/G]CCTTCTGGTAATGAA | 51096 |
rs201007115 | snp | C/T | 0.000577726 | 0.0169861 | intron-variant | UTP18 | GRCh38.p7 | 17:51266165 | GTTATTTAAAATATG[C/T]TGTTCTGTTTTTGTA | 51096 |
rs201035528 | snp | C/T | | | synonymous-codon | UTP18 | GRCh38.p7 | 17:51277255 | CAGCAAGGTTCTTTA[C/T]GTCTATGACATGCTG | 51096 |
rs201072443 | snp | A/G | 1.74033e-05 | 0.0029498 | synonymous-codon | UTP18 | GRCh38.p7 | 17:51280027 | AGAGAAGATAGTGAG[A/G]AGCTTTGAAGTCTCC | 51096 |
rs201141269 | in-del | -/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51293504 | ACATGAGTTGTTGTT[-/G]TTTTTTTTTTTTAAG | 51096 |
rs201169817 | snp | C/T | 6.91284e-05 | 0.00587873 | utr-variant-5-prime, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51260558 | GAGGTTCCACGTGAG[C/T]GCCTGCGTTTCTCCT | 51096 |
rs201171372 | snp | G/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51275242 | ATAAAAATTTAACTT[G/T]GTGGTTACAAACAAA | 51096 |
rs201195787 | in-del | -/T | 0.0829062 | 0.185956 | intron-variant, downstream-variant-500B | UTP18 | GRCh38.p7 | 17:51286831 | TAAGTAGTTTTTAAA[-/T]TTTTTTTATTATACT | 51096 |
rs201245176 | in-del | -/C | 0.402982 | 0.197728 | intron-variant | UTP18 | GRCh38.p7 | 17:51264690 | TTTAGTCATTGTCTT[-/C]TTTTTTTTTTTTTTG | 51096 |
rs201409207 | snp | A/G | 0.000408247 | 0.0142813 | missense, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51260814 | TCCGGCAGCGGAACC[A/G]CCTGAGGCTGGAGGA | 51096 |
rs201423752 | in-del | -/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51268014 | TGTTTTTTGTTTTTT[-/G]TTTTTTTTTTTTTGA | 51096 |
rs201471610 | snp | G/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51267459 | CTAAAACTTTTTTTT[G/T]GGTTTTTTTTTTTTT | 51096 |
rs201491645 | snp | A/G | 0.000165599 | 0.0090979 | missense | UTP18 | GRCh38.p7 | 17:51285320 | ATGAAGGCAGTTTAT[A/G]TGGATTAAGCATTGC | 51096 |
rs201587480 | in-del | -/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51267450 | ATCTAGTTCTAAAAC[-/T]TTTTTTTTTGGTTTT | 51096 |
rs201600029 | snp | A/G | 3.3227e-05 | 0.00407583 | missense | UTP18 | GRCh38.p7 | 17:51275938 | GTGCAGTTCCATCCC[A/G]GTGCACAGATTGTGA | 51096 |
rs201631632 | snp | G/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51276163 | ATTTACTTGGAAATA[G/T]AAAACAGAACATCCA | 51096 |
rs201637382 | snp | C/T | 0.000116197 | 0.00762135 | missense | UTP18 | GRCh38.p7 | 17:51268851 | GATTCCAACATGCCA[C/T]GGGAGGAGTACCTGC | 51096 |
rs201744084 | in-del | -/T | 0.0115144 | 0.0749975 | intron-variant | UTP18 | GRCh38.p7 | 17:51262611 | CAATTCTCCGAACAC[-/T]TTAAACTCAGAAGTC | 51096 |
rs201811541 | snp | C/T | | | synonymous-codon | UTP18 | GRCh38.p7 | 17:51277285 | GGCTGGAAAGTTAAT[C/T]CCTGTGCATCAAGTG | 51096 |
rs201872601 | snp | G/T | | | intron-variant, downstream-variant-500B | UTP18 | GRCh38.p7 | 17:51289200 | CTTTCTGTTTTTTTT[G/T]TTTTTTTTTTTTTTG | 51096 |
rs201887137 | snp | C/T | 1.65847e-05 | 0.0028796 | synonymous-codon | UTP18 | GRCh38.p7 | 17:51273388 | GAGGATGAAGATGAT[C/T]TGTTGCAAAGGACTG | 51096 |
rs201970296 | snp | C/T | 0.00124795 | 0.0249483 | utr-variant-3-prime | UTP18 | GRCh38.p7 | 17:51296996 | GACTTCTAAAGAGAC[C/T]ATTTGAAGTAAGAAA | 51096 |
rs202052301 | in-del | -/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51279512 | TTGTTTTTTGTTTTT[-/G]TTTTTGACTCACAAA | 51096 |
rs202139676 | in-del | -/TTTTG | | | intron-variant | UTP18 | GRCh38.p7 | 17:51282327 | TAGCTTAACATTAAT[-/TTTTG]TTTTGTTTTTGTCCT | 51096 |
rs202187776 | snp | A/G | 0.00199806 | 0.0315443 | missense | UTP18 | GRCh38.p7 | 17:51280066 | GTCCTTCTTGCTCAT[A/G]AATGGCATTGCTGGA | 51096 |
rs202204096 | snp | C/G | 0.000469775 | 0.0153188 | synonymous-codon | UTP18 | GRCh38.p7 | 17:51294037 | AAAGGGCAAGGCCCT[C/G]ATGTATAGGTAGGTA | 51096 |
rs267604957 | snp | C/T | | | missense | UTP18 | GRCh38.p7 | 17:51263334 | GCAAAAGGTAATTTT[C/T]CACCTCAAAAGAAGC | 51096 |
rs367563218 | snp | C/T | | | intron-variant, downstream-variant-500B | UTP18 | GRCh38.p7 | 17:51289529 | TTCTAAGGATAGCAG[C/T]CTTGGGCCTATGTAA | 51096 |
rs367584921 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51277834 | TATCTGCCCTCTACC[A/G]TACCCATTCTTTTCC | 51096 |
rs367589134 | in-del | -/CTA | | | intron-variant | UTP18 | GRCh38.p7 | 17:51279153 | CACGGTGTTAAAAAT[-/CTA]CTATGTAGAAATGAA | 51096 |
rs367592431 | snp | C/T | 1.65622e-05 | 0.00287764 | missense | UTP18 | GRCh38.p7 | 17:51277236 | TTTTAGCCACGAGTA[C/T]CCACAGCAAGGTTCT | 51096 |
rs367594840 | snp | A/G | | | missense, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51260637 | GGAGAACCGGAGCGA[A/G]GCCGAAGCGGAAGCC | 51096 |
rs367739676 | snp | C/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51265799 | GATCTCTTGACCTCG[C/T]GATCCACCTGCCTCA | 51096 |
rs367882219 | snp | A/C/T | 0.000222683 | 0.0105496 | intron-variant | UTP18 | GRCh38.p7 | 17:51280485 | GCCTCTTCGGGTAAG[A/C/T]CAACGACATGAAAGA | 51096 |
rs368023707 | snp | C/G | 4.96989e-05 | 0.00498467 | missense | UTP18 | GRCh38.p7 | 17:51263295 | GAACATGAAGACTCG[C/G]GTGACTCAGAAGTGG | 51096 |
rs368049556 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51278136 | TCTTTTCTTTCCTGT[A/G]TTCCTGACACTTTGA | 51096 |
rs368179883 | snp | A/G | | | intron-variant, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51261038 | GCGGGGAGCGCTCAG[A/G]TGGGAGGGAGCCCGA | 51096 |
rs368215921 | snp | C/T | 8.28796e-05 | 0.00643684 | intron-variant | UTP18 | GRCh38.p7 | 17:51285230 | AACAACTCTTTTTTT[C/T]GCTCTTTTATGCAGG | 51096 |
rs368250452 | snp | C/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51264196 | CGTGTGCCACCACAC[C/G]TGGCTAATTTTTGTA | 51096 |
rs368488479 | snp | C/G | 0.000153164 | 0.00874978 | intron-variant | UTP18 | GRCh38.p7 | 17:51277090 | CAGGATACAGGGTCT[C/G]TGGAAATAATCAAAA | 51096 |
rs368653640 | in-del | -/AAAAG | | | intron-variant | UTP18 | GRCh38.p7 | 17:51291750 | TCTCAAAAAAAAAAA[-/AAAAG]AAAAGAAAAGAAAAG | 51096 |
rs368750762 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51282163 | GACTTTCAAGTGGTT[C/T]TGCTCTGTGGGTAGT | 51096 |
rs368767540 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51276724 | TCTGCTCTTGGATAG[A/G]GTATCCCAGTTTTCT | 51096 |
rs368863426 | snp | C/T | 1.65811e-05 | 0.00287929 | missense | UTP18 | GRCh38.p7 | 17:51277290 | GAAAGTTAATTCCTG[C/T]GCATCAAGTGAGAGG | 51096 |
rs368866462 | snp | A/G | 1.72121e-05 | 0.00293356 | missense | UTP18 | GRCh38.p7 | 17:51280050 | AAGTCTCCCCAGATG[A/G]GTCCTTCTTGCTCAT | 51096 |
rs368888047 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51278612 | CTCCTTTTTCTGTTT[G/T]CACATTTCCACCGCC | 51096 |
rs368889003 | snp | G/T | 0.0821764 | 0.185298 | intron-variant | UTP18 | GRCh38.p7 | 17:51295227 | CATTTGTCAATTTTG[G/T]CTTTTGTTGCCATTG | 51096 |
rs368920064 | snp | A/G | | | upstream-variant-2KB, intron-variant | UTP18, MBTD1 | GRCh38.p7 | 17:51259775 | GGGTTCCTGGGGTCG[A/G]AGAGCTGCAGGCGTC | 51096 |
rs368922442 | snp | A/T | | | intron-variant, downstream-variant-500B | UTP18 | GRCh38.p7 | 17:51289371 | CCAGCTCATTTTTGT[A/T]TTTTTTTTTTTTTTT | 51096 |
rs368934447 | snp | C/G/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51270938 | CTTGTTGAAGGTATA[C/G/T]TTATTGTTGACAGAA | 51096 |
rs368950763 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51288285 | ACAGGAAAGGAGAGC[A/G]TTGAATTATTTTTAA | 51096 |
rs369063333 | snp | C/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51292766 | TGGGTGAGGACCTGT[C/T]TCAACTCTCCTGAAC | 51096 |
rs369218604 | snp | C/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51283904 | ACAGGCATGAGCCAC[C/T]ATGCCTGGCCATCTC | 51096 |
rs369267009 | snp | C/G/T | 7.54942e-05 | 0.00614348 | intron-variant | UTP18 | GRCh38.p7 | 17:51288013 | TTAATCTATTTTAAT[C/G/T]CTTTTCTCTTTGTAG | 51096 |
rs369297289 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UTP18 | GRCh38.p7 | 17:51292143 | AATTTTGCAATATCC[A/G]TGTTGTGGCTTCTCT | 51096 |
rs369418338 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | UTP18 | GRCh38.p7 | 17:51266954 | ACCTCTATCTCCTGG[A/G]CTCCCCATAGCTGGG | 51096 |
rs369421344 | snp | C/T | 0.000206526 | 0.0101597 | intron-variant | UTP18 | GRCh38.p7 | 17:51293888 | CACTTTAAAGTTTTT[C/T]ATTATCTCCTGCAGG | 51096 |
rs369517713 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | UTP18 | GRCh38.p7 | 17:51295739 | CAATTCTGTGAAGAA[A/G]GTCATTGGTAGCTTG | 51096 |
rs369533091 | snp | C/G | | | intron-variant, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51262274 | TATCTTTAGTAGAAA[C/G]GGGGTTTCACCATCT | 51096 |
rs369543955 | snp | A/C | | | upstream-variant-2KB, intron-variant | UTP18, MBTD1 | GRCh38.p7 | 17:51258888 | CTCACTATCTCTCAA[A/C]CCCCCTTCCTCCACT | 51096 |
rs369675578 | snp | C/T | 1.66443e-05 | 0.00288477 | intron-variant | UTP18 | GRCh38.p7 | 17:51277324 | GATTTCTGTTGAATG[C/T]ACACAACCAGTCATT | 51096 |
rs369720382 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51275562 | TTTGGGGAAATGACT[A/G]CATACTAGTGCTCCA | 51096 |
rs369856617 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51279726 | GAAAATTAGTTGATA[C/T]GTTTACTGTTTGGAG | 51096 |
rs369888880 | snp | A/G | 0.000833637 | 0.0203991 | missense, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51260759 | CCGAGCGCGGCGGCC[A/G]CTGCGATTGCAGTCG | 51096 |
rs369956662 | snp | C/T | 0.0114292 | 0.0747259 | synonymous-codon, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51260740 | GCGGAAACCGCCGGC[C/T]CGGCCGAGCGCGGCG | 51096 |
rs370008750 | in-del | -/GC/T | | | intron-variant, downstream-variant-500B | UTP18 | GRCh38.p7 | 17:51286983 | CCTCCCCCTTCCCCC[-/GC/T]CCCGACCCACAGGCC | 51096 |
rs370056458 | snp | C/T | 7.54603e-05 | 0.00614202 | synonymous-codon, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51260890 | CGACGTCGAGAACGA[C/T]GAGGACGCGTTGCTG | 51096 |
rs370064475 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant, downstream-variant-500B | UTP18 | GRCh38.p7 | 17:51289346 | GGATTATAGGCATGC[A/G]CCACCACGCCCAGCT | 51096 |
rs370069462 | snp | A/G | 0.000115969 | 0.00761387 | intron-variant | UTP18 | GRCh38.p7 | 17:51280113 | CAATGAAGGTAAAGC[A/G]TTATTATTGCTTCTT | 51096 |
rs370081332 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | UTP18 | GRCh38.p7 | 17:51279425 | ATATGATTTGGTTAC[A/C]TGTGTCACATCCAGA | 51096 |
rs370084996 | snp | A/C | | | intron-variant, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51262496 | GGTCTAACTTTGTCA[A/C]CCAGACTGGAGTGTA | 51096 |
rs370136854 | in-del | -/A | | | intron-variant, downstream-variant-500B | UTP18 | GRCh38.p7 | 17:51286830 | TAAGTAGTTTTTAAA[-/A]TTTTTTTTATTATAC | 51096 |
rs370144932 | snp | A/G | 5.08246e-05 | 0.00504081 | missense | UTP18 | GRCh38.p7 | 17:51280470 | AGTAAGAAAGTATAC[A/G]CCTCTTCGGGTAAGA | 51096 |
rs370195356 | snp | C/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51276639 | CAGGATGTCACTCTC[C/T]GATGGGGGTATAGAT | 51096 |
rs370204120 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51291264 | AAATGGGGGCTATAA[A/G]TAGATGTCAGAGCAC | 51096 |
rs370207136 | snp | A/G | | | upstream-variant-2KB, intron-variant | UTP18, MBTD1 | GRCh38.p7 | 17:51259712 | CTCCGGAGGTTGAGA[A/G]GGCGTGGGATGGAGA | 51096 |
rs370210639 | in-del | -/A | | | intron-variant | UTP18 | GRCh38.p7 | 17:51285062 | GAAAAACTGCATCTC[-/A]AAAAAAAAAAAAGGA | 51096 |
rs370243801 | snp | A/C | 0.000169986 | 0.00921758 | intron-variant | UTP18 | GRCh38.p7 | 17:51294082 | AAGTCAGAGATACCT[A/C]TAAACTACTTCTGAC | 51096 |
rs370338512 | in-del | -/ATATTT | | | intron-variant | UTP18 | GRCh38.p7 | 17:51295855 | ACCTGGGGAATATAT[-/ATATTT]TTTGGAAAGCACTAT | 51096 |
rs370389332 | snp | C/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51276330 | TATGACTTCAGTGTA[C/T]AAGGAACCATAATAA | 51096 |
rs370396250 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51272402 | CCGCGCCTGGCCTGA[A/G]CATAGTATTTTTAAG | 51096 |
rs370461724 | snp | C/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51275080 | CACATGTCTGTAATC[C/G]CAGCTACTTGGGAGG | 51096 |
rs370504798 | snp | C/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51269367 | AGGTTTTAAATTTAA[C/T]TTGTACCATGGCTAT | 51096 |
rs370735759 | snp | A/G | 6.62515e-05 | 0.00575512 | missense | UTP18 | GRCh38.p7 | 17:51277203 | TTAAGGCTTGTTTTA[A/G]TGCTAATGGGGAAGA | 51096 |
rs370798631 | snp | A/C | | | upstream-variant-2KB, utr-variant-5-prime | UTP18, MBTD1 | GRCh38.p7 | 17:51260137 | TCCTCTCTCGCTTCC[A/C]CCGTGGGACCCTCTG | 51096 |
rs370860955 | snp | C/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51271781 | CAAATGATTCTCCTG[C/T]CTCAGCCACCCAAGT | 51096 |
rs370876378 | snp | A/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51282540 | GAAAGAAAGAAAGAA[A/T]GAATTAGTTCAGAGT | 51096 |
rs370905981 | snp | A/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51268986 | TTTCTTATGAGGCTC[A/T]TTAAAACCTGGCATT | 51096 |
rs370949041 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UTP18 | GRCh38.p7 | 17:51287679 | TGGTGGGTGATAGGT[A/G]GTCTGTGGGAGTAAA | 51096 |
rs370975320 | snp | C/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51279752 | TGGAGAGCTGAGTCT[C/G]TGGCCTGCAGTTAAA | 51096 |
rs371007831 | snp | A/G | | | synonymous-codon | UTP18 | GRCh38.p7 | 17:51280442 | GGTTGCAGCATCCAC[A/G]TTCTCTTCAGATAGT | 51096 |
rs371019293 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51290525 | TTGATAAATGAGAAG[A/G]TTCTAATTCAAGTCA | 51096 |
rs371046566 | snp | G/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51268000 | AGTTGTTGTTTTTTT[G/T]TTTTTTGTTTTTTGT | 51096 |
rs371073346 | snp | A/G | 1.89209e-05 | 0.00307573 | intron-variant | UTP18 | GRCh38.p7 | 17:51280348 | GTGTGATTCTTCTGT[A/G]TACTTTCTAACAGTT | 51096 |
rs371183559 | snp | C/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51276804 | TCTTATCTCCTTATC[C/T]GTGGGTGGACAAACT | 51096 |
rs371259677 | snp | C/T | 3.31587e-05 | 0.00407164 | intron-variant | UTP18 | GRCh38.p7 | 17:51263268 | AGGGTGTTTTGTCTG[C/T]TGTAGGTTCAAGAAC | 51096 |
rs371342888 | snp | C/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51265351 | TCACTGCAGCTTCTG[C/T]TTCCCAGGTTCAAGT | 51096 |
rs371369286 | snp | A/G | 0.118584 | 0.212673 | intron-variant | UTP18 | GRCh38.p7 | 17:51294830 | ACCAACAGTGTAAAA[A/G]TGTTCCTATTTCTCC | 51096 |
rs371437894 | in-del | -/C/CTGTACTTCAGTCTGG | | | intron-variant | UTP18 | GRCh38.p7 | 17:51271581 | AGTCTGGGTATATTT[-/C/CTGTACTTCAGTCTGG]TTCTGATTCGTTTTC | 51096 |
rs371445294 | snp | C/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51269572 | ATGTCCGTAGAGCTT[C/G]AGTTTGATTATGACC | 51096 |
rs371456213 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UTP18 | GRCh38.p7 | 17:51294549 | ATTTTTTATGGCTGC[A/G]TAGTATTCCATGGTG | 51096 |
rs371571229 | snp | C/G | 0.000100197 | 0.00707732 | intron-variant | UTP18 | GRCh38.p7 | 17:51277344 | AACCAGTCATTCCCC[C/G]CAAGGTGAGTTTATG | 51096 |
rs371623043 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51281414 | AAAATAAAATTTTAC[A/G]TGCCTTTTTTTCTCT | 51096 |
rs371628195 | snp | A/C/G | 7.29812e-05 | 0.00604037 | synonymous-codon, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51260623 | AATGAAACTGGACCG[A/C/G]AGAACCGGAGCGAAG | 51096 |
rs371630725 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51265344 | TCTTGGCTCACTGCA[A/G]CTTCTGCTTCCCAGG | 51096 |
rs371682748 | in-del | CTGTACTTCAGTCTGGG/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51271582 | AGTCTGGGTATATTT[CTGTACTTCAGTCTGGG/T]TCTGATTCGTTTTCT | 51096 |
rs371729988 | snp | A/G | | | intron-variant, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51261330 | TGGGCACGGGCCTGG[A/G]CATCTCCGTTGTAAC | 51096 |
rs371731234 | snp | A/G | 4.96882e-05 | 0.00498414 | missense | UTP18 | GRCh38.p7 | 17:51277260 | AGGTTCTTTATGTCT[A/G]TGACATGCTGGCTGG | 51096 |
rs371773701 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | UTP18 | GRCh38.p7 | 17:51277882 | TTATATCCCAAAATA[C/G]ACCGACACCTTCATG | 51096 |
rs371780348 | in-del | -/A | | | intron-variant | UTP18 | GRCh38.p7 | 17:51281164 | TATATATATATATAT[-/A]TTTTTTTTAAACGAA | 51096 |
rs371798813 | snp | A/G | 0.000110564 | 0.00743438 | missense, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51260598 | CGATGCCGCCGGAGC[A/G]GAGGAGACGAATGAA | 51096 |
rs371809988 | snp | A/G | 1.66521e-05 | 0.00288544 | utr-variant-3-prime | UTP18 | GRCh38.p7 | 17:51296997 | ACTTCTAAAGAGACT[A/G]TTTGAAGTAAGAAAA | 51096 |
rs371867587 | snp | G/T | 0.000505872 | 0.0158959 | missense, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51260650 | GAAGCCGAAGCGGAA[G/T]CCCGGAATGAGGCCG | 51096 |
rs371998698 | snp | G/T | 3.31483e-05 | 0.004071 | intron-variant | UTP18 | GRCh38.p7 | 17:51285231 | ACAACTCTTTTTTTC[G/T]CTCTTTTATGCAGGG | 51096 |
rs372080531 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51291947 | AACAGCTTTGTCCTC[A/G]CCCCTTGTAGCAAAT | 51096 |
rs372141454 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51283288 | ATTCTCCTGCCTCAG[C/T]CTCCTGGGTAGCTGG | 51096 |
rs372298440 | snp | A/C | | | downstream-variant-500B | UTP18 | GRCh38.p7 | 17:51297978 | CAACACACACACACA[A/C]AAACTTGGATGCATT | 51096 |
rs372336254 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | UTP18 | GRCh38.p7 | 17:51268076 | GTGCAGCGGCGTGAT[C/T]GCGGCTCACTGCAAG | 51096 |
rs372541415 | snp | A/C/G | 0.000317943 | 0.012605 | missense | UTP18 | GRCh38.p7 | 17:51280080 | TAAATGGCATTGCTG[A/C/G]ATATTTGCATTTGCT | 51096 |
rs372559508 | snp | C/T | | | intron-variant, missense | UTP18 | GRCh38.p7 | 17:51286674 | TTTCCTACCCATACC[C/T]GTGCCAACCCTGTAG | 51096 |
rs372702925 | in-del | -/A | | | intron-variant, utr-variant-3-prime | UTP18 | GRCh38.p7 | 17:51288892 | TTTAATTCCTCCAGT[-/A]AATGAGTTGTAACAA | 51096 |
rs372710767 | snp | G/T | 0.000145555 | 0.00852973 | intron-variant | UTP18 | GRCh38.p7 | 17:51280522 | GGATATTTTTACATT[G/T]TAAATTTTAGGCCAG | 51096 |
rs372736058 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | UTP18 | GRCh38.p7 | 17:51280849 | GCCATCTATCCTGGG[C/T]GACAGAGCAAGACTC | 51096 |
rs372766030 | snp | C/G/T | 0.000789687 | 0.0198558 | synonymous-codon, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51260776 | TGCGATTGCAGTCGC[C/G/T]GCGGCGGAGGAAGAG | 51096 |
rs372872788 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51297104 | CTTTGTTTCTCTACC[C/T]CTAAGTTACTGCATC | 51096 |
rs373145760 | snp | G/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51268007 | GTTTTTTTGTTTTTT[G/T]TTTTTTGTTTTTTTT | 51096 |
rs373205291 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51278717 | TGTCCTACCTCATCA[C/T]GTAATGATATTTTCT | 51096 |
rs373219166 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UTP18 | GRCh38.p7 | 17:51267514 | CAAAAGAAAACTCTC[C/T]ATTAATTAGTCACTT | 51096 |
rs373233062 | snp | C/G | | | upstream-variant-2KB, intron-variant | UTP18, MBTD1 | GRCh38.p7 | 17:51259384 | CCACGTGCAAACCGC[C/G]TCGCGGCACTGCCCC | 51096 |
rs373296052 | in-del | -/AAAAA | | | intron-variant | UTP18 | GRCh38.p7 | 17:51291749 | ATCTCAAAAAAAAAA[-/AAAAA]GAAAAGAAAAGAAAA | 51096 |
rs373722406 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime | UTP18, MBTD1 | GRCh38.p7 | 17:51260272 | TTCAGCCGTCCCAGT[A/G]TATAGTCGGGGTTTC | 51096 |
rs373768555 | snp | C/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51295905 | ATTGAGAAAAAGCCA[C/T]TTTAATAATATTTCC | 51096 |
rs373854882 | snp | C/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51272596 | GGTTTATATGTTTAC[C/T]TCTAGGTAGGTAGCT | 51096 |
rs374030427 | in-del | -/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51271342 | ACAGGGTCTCACTCT[-/T]ATCGCCCAGTCTGGA | 51096 |
rs374030862 | snp | C/T | | | upstream-variant-2KB, intron-variant | UTP18, MBTD1 | GRCh38.p7 | 17:51259457 | GCTCCCCCTCCCCGC[C/T]AAGAAGAGAGGACTA | 51096 |
rs374061305 | snp | A/G | 4.98774e-05 | 0.00499362 | synonymous-codon | UTP18 | GRCh38.p7 | 17:51293992 | CATGGATTTTTCTCC[A/G]AGAAGTGGATACTTT | 51096 |
rs374145838 | snp | G/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51274456 | TTTGTTTGTTTGTTT[G/T]TTTGAGACAGAGTTT | 51096 |
rs374239641 | snp | A/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51283617 | TTTGTTTACTCATGG[A/T]TTTTTTTTTTTTTTT | 51096 |
rs374245189 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51279933 | AAAAGTAAGAAACTC[A/G]TTTGTCAATAGATGA | 51096 |
rs374301359 | snp | A/G | 5.10521e-05 | 0.00505207 | synonymous-codon | UTP18 | GRCh38.p7 | 17:51280478 | AGTATACGCCTCTTC[A/G]GGTAAGACAACGACA | 51096 |
rs374336052 | snp | C/G | | | intron-variant, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51260995 | GGCGGTGAAGCTCCG[C/G]GGGGCGGAGCCTGGG | 51096 |
rs374344490 | snp | C/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51295294 | CTATGTCCTGAATGG[C/T]ATTGCCTAGGTTTTC | 51096 |
rs374353115 | snp | A/C | | | intron-variant | UTP18 | GRCh38.p7 | 17:51275165 | TTACGCCATTGCCCT[A/C]CAGCCTGGGCAACAA | 51096 |
rs374478611 | snp | A/C | | | downstream-variant-500B | UTP18 | GRCh38.p7 | 17:51297980 | ACACACACACACACA[A/C]ACTTGGATGCATTTA | 51096 |
rs374487789 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51289735 | GTACTACCAGATTGT[A/G]CGCACTTTACAAAGT | 51096 |
rs374504984 | snp | A/G | | | upstream-variant-2KB, intron-variant | UTP18, MBTD1 | GRCh38.p7 | 17:51259720 | GTTGAGAGGGCGTGG[A/G]ATGGAGAAGCAGGCC | 51096 |
rs374505525 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51271343 | ACAGGGTCTCACTCT[A/G]TCGCCCAGTCTGGAG | 51096 |
rs374575166 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51292757 | TCCACAAATTGGGTG[A/G]GGACCTGTCTCAACT | 51096 |
rs374587954 | snp | C/G/T | 0.0158118 | 0.0875064 | intron-variant, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51260948 | GAGGCCGCGGCGCGC[C/G/T]GGCTGGGCGCACTCG | 51096 |
rs374805293 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51281632 | AACAGGAGGGGTCCT[C/G/T]GTGGTGATGGGAAGT | 51096 |
rs374934194 | in-del | -/GTCAA | 0.00438332 | 0.0466095 | upstream-variant-2KB, utr-variant-5-prime | UTP18, MBTD1 | GRCh38.p7 | 17:51260213 | CGTATTGGGGCTTGT[-/GTCAA]GTCAAGTGGTTACAG | 51096 |
rs374988637 | snp | A/C/T | 3.44064e-05 | 0.00414756 | synonymous-codon | UTP18 | GRCh38.p7 | 17:51280042 | GAGCTTTGAAGTCTC[A/C/T]CCAGATGGGTCCTTC | 51096 |
rs375019921 | in-del | -/A | | | intron-variant, downstream-variant-500B | UTP18 | GRCh38.p7 | 17:51286830 | ATAAGTAGTTTTTAA[-/A]TTTTTTTTATTATAC | 51096 |
rs375134330 | snp | G/T | 1.69341e-05 | 0.00290977 | intron-variant | UTP18 | GRCh38.p7 | 17:51273311 | TTGGGGTAGGTAAAA[G/T]GGGCAGCTCATTGAT | 51096 |
rs375137994 | snp | A/G | 1.89059e-05 | 0.00307451 | intron-variant | UTP18 | GRCh38.p7 | 17:51280350 | GTGATTCTTCTGTAT[A/G]CTTTCTAACAGTTTG | 51096 |
rs375350032 | snp | A/C | 0.000165986 | 0.00910853 | missense | UTP18 | GRCh38.p7 | 17:51277219 | TGCTAATGGGGAAGA[A/C]GTTTTAGCCACGAGT | 51096 |
rs375359430 | snp | G/T | | | upstream-variant-2KB, utr-variant-5-prime | UTP18, MBTD1 | GRCh38.p7 | 17:51260436 | GGGAGCGGGAGTTAC[G/T]TAGAGGGAGGGAGTG | 51096 |
rs375404820 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51265125 | CCCAGCTTTCTGTGC[A/G]TAGAAGTTTTGAATT | 51096 |
rs375424549 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51278318 | TGGTGATACTGTGTG[A/G]TCCATGGACCTCACT | 51096 |
rs375532632 | snp | C/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51279779 | TAAAATGGTGAATGC[C/T]AACCAGGACAAAGAA | 51096 |
rs375573669 | snp | C/T | 0.00318978 | 0.0398085 | upstream-variant-2KB, intron-variant | UTP18, MBTD1 | GRCh38.p7 | 17:51259664 | GGGGAGGGGAACCCC[C/T]GAATCGTTTAACGGC | 51096 |
rs375856552 | snp | G/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51278534 | CTGCTAGGTGGGCAG[G/T]AGTGTGTGTCCAGTC | 51096 |
rs375915701 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | UTP18 | GRCh38.p7 | 17:51266503 | CAAATATAATCAGTG[A/T]TAATATTGCTTACTT | 51096 |
rs376022224 | snp | C/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51283683 | CAGTGGTGTGATCTT[C/G]GCTCACTACATCCTC | 51096 |
rs376100840 | snp | A/C | | | intron-variant | UTP18 | GRCh38.p7 | 17:51263075 | TCCATCTTGCCTCAC[A/C]TGTCCAGTCGGTGCC | 51096 |
rs376141133 | snp | G/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51273598 | AATACTTATGTTATT[G/T]TTTTTTTTTTTTCCT | 51096 |
rs376256071 | snp | C/G | 3.65878e-05 | 0.00427698 | missense, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51260628 | AACTGGACCGGAGAA[C/G]CGGAGCGAAGCCGAA | 51096 |
rs376401119 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51274519 | TGATCTCGGCTCACT[A/G]CAACCTCCGCCTCCC | 51096 |
rs376484199 | snp | C/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51296317 | CTTTAGGGAATTCCT[C/G]CTTTCAAAACGGACT | 51096 |
rs376510774 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51283717 | CTCCTGGGTTCAGGC[G/T]ATTCTCATGCCTCAG | 51096 |
rs376542901 | snp | A/G | 1.68176e-05 | 0.00289974 | missense | UTP18 | GRCh38.p7 | 17:51266191 | TTGTAGGGTTGACAT[A/G]ATGAACAATCGGTTT | 51096 |
rs376669921 | snp | G/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51279957 | TAGATGATAGTTTTA[G/T]TGAAAACTATATAAA | 51096 |
rs376721463 | in-del | -/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51281164 | ATATATATATATATA[-/T]TTTTTTTTAAACGAA | 51096 |
rs376872213 | snp | C/G/T | 5.39121e-05 | 0.00519169 | synonymous-codon, missense | UTP18 | GRCh38.p7 | 17:51280090 | TGCTGGATATTTGCA[C/G/T]TTGCTAGCAATGAAG | 51096 |
rs376890315 | snp | A/C | | | intron-variant | UTP18 | GRCh38.p7 | 17:51277008 | TGGCCGTGGCTGCTT[A/C]AGTCAGCCTTCAGCC | 51096 |
rs376900305 | snp | A/G | | | missense, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51260607 | CGGAGCGGAGGAGAC[A/G]AATGAAACTGGACCG | 51096 |
rs376937133 | snp | A/G | 1.66258e-05 | 0.00288316 | missense | UTP18 | GRCh38.p7 | 17:51293997 | ATTTTTCTCCGAGAA[A/G]TGGATACTTTGCCTT | 51096 |
rs376949492 | snp | A/G | | | intron-variant, downstream-variant-500B | UTP18 | GRCh38.p7 | 17:51289315 | GATTCTTCTGCCTCA[A/G]TCTCCTGAGTAGCTG | 51096 |
rs377009361 | snp | A/T | 3.46069e-05 | 0.0041596 | intron-variant | UTP18 | GRCh38.p7 | 17:51293874 | GCTCCCAGTTGTTAC[A/T]CTTTAAAGTTTTTTA | 51096 |
rs377075898 | snp | A/C/T | 0.000188377 | 0.00970325 | missense, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51260745 | AACCGCCGGCCCGGC[A/C/T]GAGCGCGGCGGCCGC | 51096 |
rs377108748 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51268957 | TCCCTGTTCCTGTTC[A/G]TTATTATTTGAGCTT | 51096 |
rs377163872 | snp | C/G | 1.65647e-05 | 0.00287786 | synonymous-codon | UTP18 | GRCh38.p7 | 17:51277270 | TGTCTATGACATGCT[C/G]GCTGGAAAGTTAATT | 51096 |
rs377167917 | snp | A/G | 4.00192e-05 | 0.00447303 | missense, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51260661 | GGAAGCCCGGAATGA[A/G]GCCGGACTGGAAAGC | 51096 |
rs377210451 | snp | C/T | 0.000167986 | 0.00916322 | missense, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51260844 | AGGACAAACCGGCCG[C/T]GGAGCGGTGCTTGGA | 51096 |
rs377226418 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51291000 | TCGACAATTTTGGAT[A/G]TAGTAGAACGTCATG | 51096 |
rs377294091 | snp | C/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51295581 | TTTTGGTACCAGTAC[C/T]CTGCTGTTTTGGTTA | 51096 |
rs377302912 | snp | C/T | 6.48978e-05 | 0.00569603 | intron-variant | UTP18 | GRCh38.p7 | 17:51280141 | CTTGTTCTTCTCCCA[C/T]AAGACACTAGTGTAG | 51096 |
rs377441323 | snp | G/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51267475 | GGTTTTTTTTTTTTT[G/T]GTTCTTAAACATTTT | 51096 |
rs377481778 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UTP18 | GRCh38.p7 | 17:51279552 | GAGATTCCTGTCCAT[C/T]ATGAGCTGCTTAGTA | 51096 |
rs377540818 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51269258 | GTGATAAGTGCCACC[A/G]TACTCCAGCCTGGGT | 51096 |
rs377548364 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51284915 | AAAATACAAAAATTA[A/G]CTACGCATGGTGGCA | 51096 |
rs377678580 | snp | C/T | 0.000136105 | 0.00824828 | intron-variant | UTP18 | GRCh38.p7 | 17:51293900 | TTTTATTATCTCCTG[C/T]AGGTTCATCTTCCTT | 51096 |
rs377737593 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51275296 | AATTTTAAAAATTCA[A/G]GGGGAAACCTGTAAA | 51096 |
rs386386250 | in-del | -/TT | | | intron-variant, downstream-variant-500B | UTP18 | GRCh38.p7 | 17:51289386 | TTTTTTTTTTTTTTT[-/TT]TAAGTAGAGACGGGG | 51096 |
rs397725505 | in-del | -/GA/GT/GTGA | 0 | 0 | intron-variant | UTP18 | GRCh38.p7 | 17:51269870 | TGTGTGTGTGTGTGT[-/GA/GT/GTGA]CAGTGTCAGAATCTC | 51096 |
rs397739457 | in-del | -/AG | 0 | 0 | intron-variant | UTP18 | GRCh38.p7 | 17:51276143 | TCACAGAAGTGACAG[-/AG]TTCATTTACTTGGAA | 51096 |
rs397757593 | in-del | -/T | 0 | 0 | intron-variant | UTP18 | GRCh38.p7 | 17:51281172 | ATATATATTTTTTTT[-/T]AAACGAAAAGTTGTG | 51096 |
rs397807901 | in-del | -/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51275241 | ATAAAAATTTAACTT[-/T]GGTGGTTACAAACAA | 51096 |
rs397824294 | in-del | -/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51273610 | TTGTTTTTTTTTTTT[-/T]CCTTTTGCAAAAAAT | 51096 |
rs397857848 | in-del | -/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51273201 | TTTTTTTTTTTTTTT[-/T]CCTGTTTTGCTTTTG | 51096 |
rs397973968 | in-del | -/TT | | | intron-variant, downstream-variant-500B | UTP18 | GRCh38.p7 | 17:51289387 | TTTTTTTTTTTTTTT[-/TT]AAGTAGAGACGGGGT | 51096 |
rs398031071 | in-del | -/T | 0 | 0 | intron-variant | UTP18 | GRCh38.p7 | 17:51282886 | TTTTTTTTTTTTTTT[-/T]GAGACAGAGTCTCAC | 51096 |
rs527324691 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51282424 | GGAGCAGCTATATTT[C/T]CTATATTATACTAGT | 51096 |
rs527330060 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51282751 | TCATAAGGTCCTAAG[A/G]AAGCAGGGAAGGAGA | 51096 |
rs527436043 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51263134 | TGCTTCCAGCATTTG[C/G]AATGGTAGCATTCCA | 51096 |
rs527447068 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51269368 | GGTTTTAAATTTAAC[C/T]TGTACCATGGCTATT | 51096 |
rs527497725 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51263625 | TAGCTAAGAGAATAC[A/G]GTGTTTGAAGTCAGA | 51096 |
rs527597153 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51296604 | GAAATTTTTTTTTCT[C/G]TAAGACCCAAAGGCC | 51096 |
rs527640290 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51265294 | TTGAGATGGAGTTTT[A/G]CTCTTCTTGCCTGGG | 51096 |
rs527650061 | snp | C/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51279311 | TAAGCATTTTGATAT[C/T]AGGAGGAGTCCCCTG | 51096 |
rs527709193 | snp | C/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51264161 | CCTGCCTCAGCCTCC[C/T]GAGTAGCTGTGACTA | 51096 |
rs527746086 | snp | G/T | 0.000399281 | 0.0141238 | downstream-variant-500B | UTP18 | GRCh38.p7 | 17:51298342 | GTAAACCTGGTAGCC[G/T]TGTCCTACAGATTAT | 51096 |
rs527780669 | in-del | -/TGCTAGTTGG | 0.00159617 | 0.0282053 | intron-variant | UTP18 | GRCh38.p7 | 17:51275683 | TGTGGTAAAGTGACT[-/TGCTAGTTGG]TGCCAGAGCTGCGGT | 51096 |
rs527808796 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51291273 | CTATAAATAGATGTC[A/G]GAGCACAGCATAGTT | 51096 |
rs527854967 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UTP18 | GRCh38.p7 | 17:51276535 | ATAACCTCATGACTT[C/T]ACTGGGTCTTCCATG | 51096 |
rs527873174 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UTP18 | GRCh38.p7 | 17:51292511 | AACCAGTTTAATAGG[C/T]GTATGTATCAGTGGT | 51096 |
rs527918454 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51276915 | TCCGTGTGTTCAGCA[A/C]CCCAGAAGCTCTCTG | 51096 |
rs527978274 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51264744 | CTGGAGTTCAGTGGC[A/G]CGATCTTGGCTCACT | 51096 |
rs527991719 | snp | A/G | | | intron-variant, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51261985 | CTGTTGGGTTTGAAG[A/G]CTATTAGACTAGTAG | 51096 |
rs528103192 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51272216 | TGATTCTCTTGCTTC[A/C]GCCTCCCAAGTAGCT | 51096 |
rs528168320 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | UTP18 | GRCh38.p7 | 17:51266485 | AAAAAAATTCTTACC[A/C]CTCAAATATAATCAG | 51096 |
rs528250427 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51292009 | CTTTGGATCATCTGT[C/T]CATAGTTGGGGCATG | 51096 |
rs528310210 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51284431 | ATAGATAAATTGTGT[A/G]TGTCTTCTTAATTAT | 51096 |
rs528373297 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UTP18 | GRCh38.p7 | 17:51284960 | CAGCTACTCGGGAGG[C/T]TGAGGCAGGAAAATC | 51096 |
rs528472376 | snp | C/T | 0.0010644 | 0.0230448 | synonymous-codon | UTP18 | GRCh38.p7 | 17:51293974 | TATTTCTCATGTTCA[C/T]ACCATGGATTTTTCT | 51096 |
rs528504865 | snp | A/G | | | missense | UTP18 | GRCh38.p7 | 17:51294021 | TTGCCTTGGGGAATG[A/G]AAAGGGCAAGGCCCT | 51096 |
rs528627629 | snp | A/G | | | missense | UTP18 | GRCh38.p7 | 17:51280100 | TTGCATTTGCTAGCA[A/G]TGAAGGTAAAGCATT | 51096 |
rs528641697 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51267087 | CCCACCTCAGCCTCC[C/T]GAGTAGCTGGGACTG | 51096 |
rs528712489 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51261033 | CGGCGGCGGGGAGCG[C/T]TCAGGTGGGAGGGAG | 51096 |
rs528836496 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51262326 | CCTGACCTCGTGATC[C/T]GCCCGCCTCGGCCTC | 51096 |
rs528900625 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51262994 | CTGCAGACTCATCTT[G/T]TGTTCTTGTCTTACT | 51096 |
rs528943644 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51294796 | GACTTCCACAATGGT[C/T]GAACTAGTTTACAGT | 51096 |
rs529003206 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51287652 | TTAGGACTAAAGGCA[C/G]TGATTTGGATGTGGT | 51096 |
rs529022371 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51295395 | GGTGTAAGGAAGGGA[C/T]CCAGTTTCAGCTTTC | 51096 |
rs529046150 | snp | C/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51274527 | GCTCACTGCAACCTC[C/T]GCCTCCCGGGTTCAA | 51096 |
rs529133384 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51278256 | GCAGATTCTGATTCT[A/G]TAGGTCTTAGGTGGG | 51096 |
rs529134527 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | UTP18 | GRCh38.p7 | 17:51274172 | ACCTTTGCTCTTTCT[A/C]TTTTGTTCTGCCTGC | 51096 |
rs529169033 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51261744 | TAGAGGCCTGTGAAA[G/T]TTTAGATAAAGGGGG | 51096 |
rs529242824 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51269041 | CCTGTCATCCCAGTG[A/C]TTTGGGAGCCCGAGG | 51096 |
rs529343252 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UTP18 | GRCh38.p7 | 17:51270055 | GAATCGGGGTTTCAC[C/T]GTGTTGGCCAGGCTG | 51096 |
rs529353732 | snp | C/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51272448 | TTCCGTTGTTTAGAT[C/G]CCTGTGGGGATTGTC | 51096 |
rs529382910 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51263892 | TTTAACATTTTGACT[G/T]TTTCTACATAAAGTT | 51096 |
rs529475407 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | UTP18 | GRCh38.p7 | 17:51288312 | TTAAAACAGTGGCTT[C/T]TTTTGATATAGGAAT | 51096 |
rs529536347 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51281445 | ATTCTCTCTTTTGTC[A/C]CTTGGTTTTCAGGAA | 51096 |
rs529548898 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51275183 | GCCTGGGCAACAAGA[A/G]TGAAACCCAGTCTCA | 51096 |
rs529644302 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51291059 | AGCGAGCTTTTACTT[A/G]TTGAATTTTGATATC | 51096 |
rs529821484 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51276932 | CCAGAAGCTCTCTGA[A/T]TACCTTCTGTTAAGC | 51096 |
rs529835125 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51296620 | TAAGACCCAAAGGCC[A/T]TTAGATTTTCCACCA | 51096 |
rs529867956 | snp | A/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | UTP18, MBTD1 | GRCh38.p7 | 17:51258950 | TAGGCCAATGAGCAG[A/T]GGGTGGGTGAGGAGG | 51096 |
rs529888689 | snp | C/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51291022 | AACGTCATGGAACTT[C/T]CTACCCATTAAATCA | 51096 |
rs529897087 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51297634 | AGGACAAAGGATTTT[G/T]AAAGGTACAGGCATT | 51096 |
rs529933719 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51292586 | GTCTGACCTAGAAGT[A/G]TGGAGGATGACTAAC | 51096 |
rs530001488 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | UTP18, MBTD1 | GRCh38.p7 | 17:51260140 | TCTCTCGCTTCCACC[C/G]TGGGACCCTCTGCAG | 51096 |
rs530021648 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UTP18 | GRCh38.p7 | 17:51290555 | AGCTTTAAAATCCCT[A/G]CTCCCTAATGGGAGT | 51096 |
rs530127984 | snp | A/C/T | 0.000131659 | 0.00811267 | missense, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51260589 | CAAACCTAACGATGC[A/C/T]GCCGGAGCGGAGGAG | 51096 |
rs530165834 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UTP18 | GRCh38.p7 | 17:51268083 | GGCGTGATCGCGGCT[C/G]ACTGCAAGCTCTGCC | 51096 |
rs530176649 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UTP18 | GRCh38.p7 | 17:51292141 | TAAATTTTGCAATAT[C/T]CATGTTGTGGCTTCT | 51096 |
rs530237087 | snp | A/G | 0.00119784 | 0.0244435 | intron-variant | UTP18 | GRCh38.p7 | 17:51292724 | AAGGTAACTGCTTCC[A/G]TACCTGGGTTTTATT | 51096 |
rs530259020 | snp | G/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51263492 | ATTATGTGAAGATTT[G/T]AAAAATATTTGAAAG | 51096 |
rs530275534 | in-del | -/A | | | intron-variant | UTP18 | GRCh38.p7 | 17:51291738 | GTGAGACTTGATCTC[-/A]AAAAAAAAAAAAAAA | 51096 |
rs530286777 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51277662 | CTGTTTCACCTCTCT[C/G]ATCTTCAGGAAACTT | 51096 |
rs530351451 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51265359 | GCTTCTGCTTCCCAG[A/G]TTCAAGTGATTCACC | 51096 |
rs530399400 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | UTP18 | GRCh38.p7 | 17:51272616 | GGTAGGTAGCTTGGC[A/C]GAGGACACTAGTAAT | 51096 |
rs530517746 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51261207 | CGTGAGCATCTTTCG[C/T]TGCTGCTCGACTCCG | 51096 |
rs530725676 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51272286 | GTATTTTTAGTAGAG[A/C]CGGGGTTTCTCCATG | 51096 |
rs530777265 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51285614 | TTACCTGTGGTTAAT[C/G]ACAATCTGAAATCTA | 51096 |
rs530797205 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51287378 | GAGGTCACTGCAGCA[A/G]TAGGCAGGCATCAGG | 51096 |
rs530845708 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51279295 | GAGTAACTTGGCTCT[C/T]TAAGCATTTTGATAT | 51096 |
rs531092911 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51261517 | ATCCCTTTAAATTCT[A/G]TACCAGGCTTTTCTT | 51096 |
rs531105163 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51266482 | TGGAAAAAAATTCTT[A/G]CCACTCAAATATAAT | 51096 |
rs531131385 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, missense | UTP18 | GRCh38.p7 | 17:51286726 | CCAAGCATTTACCAG[C/G]GTAGTGTGCGCTATG | 51096 |
rs531254848 | in-del | -/TTA | 0.0100216 | 0.070074 | intron-variant | UTP18 | GRCh38.p7 | 17:51288224 | TATTTCATTACCCCT[-/TTA]TTATTGTTATTTTTT | 51096 |
rs531255092 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51291132 | GCTGCGGTGGCTCAC[A/G]CCTGTAATCCCAGCA | 51096 |
rs531439211 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | UTP18 | GRCh38.p7 | 17:51289421 | ACCATTTTGGTCAGG[C/T]TGGTCTCGAACTCCC | 51096 |
rs531508964 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51268318 | GGCGTGAGCCATGGC[G/T]CCCGGCCCAGGTACC | 51096 |
rs531635586 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51263037 | TCCTGCGTGTTGAGT[A/G]TTGACTTTTTCTCCT | 51096 |
rs531687309 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51284367 | TATTTGTGCTTATTC[A/G]TAAGCTTGTGTTTAG | 51096 |
rs531692245 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UTP18 | GRCh38.p7 | 17:51265065 | TTAGTTCCTGACATA[C/T]TGAGAATTTCAAACC | 51096 |
rs531703946 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51265412 | GGGATTACAGGCTCC[C/T]GCCACCACGCTGGAC | 51096 |
rs531831624 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UTP18, MBTD1 | GRCh38.p7 | 17:51258997 | GAGAAGTAAAAAAAG[C/G]AGCAACTTAACCAGG | 51096 |
rs531848454 | snp | A/T | 0.000169678 | 0.00920926 | intron-variant | UTP18 | GRCh38.p7 | 17:51297774 | AATTTCTTTTGTTCT[A/T]TCCTCAGGTCCAGTT | 51096 |
rs531899702 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51282210 | AAAGCTTTTTAGCAT[A/T]ATTTTTATTTGACCT | 51096 |
rs531960072 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UTP18 | GRCh38.p7 | 17:51275775 | GCATTTTTTTCCTTC[A/G]TTATAAACTGTAATG | 51096 |
rs531976497 | snp | C/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51279868 | TGCGTTTAGACTTAT[C/T]CGGGGTCTGAGCCAG | 51096 |
rs532036290 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UTP18 | GRCh38.p7 | 17:51266914 | CCCAGGCTGAAATGG[A/G]GTGGTGCTGTCATGG | 51096 |
rs532038169 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UTP18 | GRCh38.p7 | 17:51277733 | GATTTATATTTAAAG[A/G]GAATAAAGCACTGCT | 51096 |
rs532098978 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51271618 | ACAAATTCTCTCTAC[A/G]GCTAATTTTGATGTA | 51096 |
rs532136148 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | UTP18 | GRCh38.p7 | 17:51268071 | CTGGAGTGCAGCGGC[A/G]TGATCGCGGCTCACT | 51096 |
rs532169991 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UTP18, MBTD1 | GRCh38.p7 | 17:51259533 | TCCAGCCTTTCCCCC[A/C]TAGCCAGAGCAGGGG | 51096 |
rs532195137 | snp | C/T | | | intron-variant, downstream-variant-500B | UTP18 | GRCh38.p7 | 17:51289546 | TTGGGCCTATGTAAA[C/T]TCTTTTCTGCCCAAC | 51096 |
rs532277935 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UTP18 | GRCh38.p7 | 17:51291898 | TAGTTTCATAGTATC[A/G]GGTGAATAGGGTGGG | 51096 |
rs532278190 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51283740 | TGCCTCAGCCTCCCC[A/G]AGTAGCTGGGATTAC | 51096 |
rs532347579 | in-del | -/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51273187 | CTTCTCCTTTAAAAT[-/T]TTTTTTTTTTTTTTC | 51096 |
rs532588687 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51285140 | TTATAATAGGTCTGT[A/G]TTTGTAGTCTCCTGT | 51096 |
rs532592941 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51293442 | GTCCAACCCACGGCG[C/T]AGGACGGTTTGATTG | 51096 |
rs532602871 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51263940 | CCCTACTTAAAAAAA[A/G]TAGACATTTTAAAAT | 51096 |
rs532617578 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51284288 | TATTGAGGTACTAGA[A/G]AAAGGAAGACGTAAA | 51096 |
rs532690556 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51272157 | AGGCTGGAGTGCAGT[C/G]GCGCAATCTCAGCTC | 51096 |
rs532702799 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51265952 | AGATAAGTCATGATG[A/G]ATTTTCTCAAATAGT | 51096 |
rs532767022 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51266401 | GGATTGCTATTGTGG[C/G]CAGTGACTAAATTTC | 51096 |
rs532767038 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | UTP18, MBTD1 | GRCh38.p7 | 17:51260159 | GACCCTCTGCAGGCT[C/G]CGTACTCCAAGGACC | 51096 |
rs532790802 | snp | C/T | | | upstream-variant-2KB, intron-variant | UTP18, MBTD1 | GRCh38.p7 | 17:51258840 | TGTAAGCCAGCACAC[C/T]TGACACTGACCCAGC | 51096 |
rs532829481 | snp | A/G | 1.8331e-05 | 0.0030274 | missense, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51260630 | CTGGACCGGAGAACC[A/G]GAGCGAAGCCGAAGC | 51096 |
rs532898378 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | UTP18 | GRCh38.p7 | 17:51294209 | TTATTTTATTTTATT[A/T]TTATTATACTTTAAG | 51096 |
rs532946905 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51279412 | ACCTAGCTCTCATAT[A/T]TGATTTGGTTACATG | 51096 |
rs533047232 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51267250 | ATACAGAGGTGAGCC[A/G]CTGTGCTCAGCCATT | 51096 |
rs533401390 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | UTP18 | GRCh38.p7 | 17:51282728 | ATGGCTGTGGAGATC[-/T]TAATTTATCATAAGG | 51096 |
rs533446992 | snp | A/C/T | 0.000180049 | 0.00948652 | intron-variant | UTP18 | GRCh38.p7 | 17:51288219 | GTAAATATTTCATTA[A/C/T]CCCTTTATTATTGTT | 51096 |
rs533451216 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51280912 | ACCAGGCGCGGTAGC[C/T]TACGCCTGTAATCCC | 51096 |
rs533458052 | snp | A/G | 0.00071573 | 0.0189038 | intron-variant | UTP18 | GRCh38.p7 | 17:51268911 | CTTCAGATGGTGAGC[A/G]TTGATATTTCTGTTT | 51096 |
rs533546593 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UTP18 | GRCh38.p7 | 17:51294735 | TAATGGGATGGCTGG[G/T]TCAAATGGTATTTCT | 51096 |
rs533749443 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51281639 | GGGGTCCTTGTGGTG[A/T]TGGGAAGTTTTGTGT | 51096 |
rs533825925 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UTP18 | GRCh38.p7 | 17:51275410 | TAAAGCAACCTGTGC[C/T]AATTGAAGAACTGTG | 51096 |
rs533877749 | snp | C/T | 4.98004e-05 | 0.00498976 | missense | UTP18 | GRCh38.p7 | 17:51275911 | CGTCCTACTGTTGCT[C/T]GGATCTCATCTGTGC | 51096 |
rs533888556 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UTP18, MBTD1 | GRCh38.p7 | 17:51259126 | TTAGGGGTGTAAGCA[A/G]GGTTCAGACTACCTA | 51096 |
rs533941130 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | UTP18 | GRCh38.p7 | 17:51297956 | ATCTGGTTCTTCCCT[C/T]CACCCCCAACACACA | 51096 |
rs533941963 | snp | A/C | | | intron-variant | UTP18 | GRCh38.p7 | 17:51285451 | TATACTAGGTGGTGC[A/C]TGAGTAGTTCTCTTT | 51096 |
rs533990176 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51294979 | CATTTTTTCATGTGT[C/T]TTTTGGCTGCATAAA | 51096 |
rs533997410 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | UTP18 | GRCh38.p7 | 17:51290796 | TTAAATGGTAGTCAA[C/G]CATAATATCTAATGG | 51096 |
rs534011573 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UTP18 | GRCh38.p7 | 17:51288283 | TAACAGGAAAGGAGA[A/G]CGTTGAATTATTTTT | 51096 |
rs534039837 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51287879 | GGTTGGAGGTTCTAT[A/T]GGACATCTGTGGCTA | 51096 |
rs534095922 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | UTP18 | GRCh38.p7 | 17:51288764 | GAACTCATGGCTAAA[A/G]TGTATTGCAGTGGAA | 51096 |
rs534100863 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UTP18 | GRCh38.p7 | 17:51269758 | TTAGAGGTTGAAGGA[A/G]TCTTAGTGATGTGGC | 51096 |
rs534102140 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UTP18 | GRCh38.p7 | 17:51281154 | AAAATATATATATAT[A/G]TATATATATATTTTT | 51096 |
rs534153455 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51264065 | TTTTTGAAACAGAGT[C/G]TTGCTGTTTCACCTA | 51096 |
rs534175274 | in-del | -/TTTTTTTTTT | 0.447809 | 0.152878 | intron-variant | UTP18 | GRCh38.p7 | 17:51282868 | TTCTTCTTCTTCTTC[-/TTTTTTTTTT]TTTTTTTTTGAGACA | 51096 |
rs534198213 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51289797 | AGCCTTGCATCTGCC[A/G]TCAGCTTTGTATTAG | 51096 |
rs534292793 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51265501 | CTCCCGACCTTCAGT[A/G]ATCCGCCTGTGTCTG | 51096 |
rs534492378 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UTP18 | GRCh38.p7 | 17:51276762 | AATAACACTTGGTCC[A/C]GTTCATGTAGTTTGG | 51096 |
rs534494320 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51283835 | GGCCAGGTTGGTCTC[A/G]AACTCCTGGCCTCAA | 51096 |
rs534621796 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UTP18 | GRCh38.p7 | 17:51271052 | TTCTCCCTTTTGAAC[A/G]TAACCACAGCTCCAA | 51096 |
rs534702440 | snp | A/C | 0.00279162 | 0.0372561 | upstream-variant-2KB, utr-variant-5-prime | UTP18, MBTD1 | GRCh38.p7 | 17:51260250 | AAGAGGAAAAGCAGA[A/C]GTTCCATTCAGCCGT | 51096 |
rs534737520 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51267792 | TTTGTGGTGGTGATG[A/G]GGTTCATCTTGCTTA | 51096 |
rs534794286 | snp | A/G | 3.67188e-05 | 0.00428463 | intron-variant | UTP18 | GRCh38.p7 | 17:51268792 | TCAAGCTTTATGGAC[A/G]TGTAGTGGTTGCCAT | 51096 |
rs534969252 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51284634 | CAATAATTTATCTGA[A/G]TGGAACTTAGAAGCT | 51096 |
rs535131477 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51272747 | CCCTTTGTGGCCGCA[A/G]TCCAAAATCTGGTGG | 51096 |
rs535197972 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51280533 | CATTTTAAATTTTAG[A/G]CCAGGCGCGGTGGCT | 51096 |
rs535265870 | snp | C/T | 0.000377477 | 0.013733 | synonymous-codon, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51260903 | GACGAGGACGCGTTG[C/T]TGCGGCGTCTGCGAG | 51096 |
rs535490622 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | UTP18 | GRCh38.p7 | 17:51286880 | TGTGCATAACGTGCA[G/T]GTTTGTTACATATGT | 51096 |
rs535526657 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51295113 | AGCCCTTTGTCAGAT[A/G]AGTAGGTTGCGACAA | 51096 |
rs535557704 | snp | A/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51273771 | AATAAATAAATAAAT[A/T]AATTTTCCAGTAATT | 51096 |
rs535608153 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UTP18 | GRCh38.p7 | 17:51267294 | GTGTTCAGACCTGTT[G/T]TCTTGTAGAATATCC | 51096 |
rs535634471 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51281000 | CTGGCCAACATGGTA[A/T]GACCCTGTCTCTGCT | 51096 |
rs535673399 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51261353 | GTTGTAACTATGTCC[C/T]CATGTGACTATGAGA | 51096 |
rs535696162 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51274487 | TGCTCTTTTGCTCAG[A/G]CTGGAGTGCAAGGGC | 51096 |
rs535732128 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51292227 | TAAAAGTAATTTCTC[A/G]AGGAACCTGTATAGA | 51096 |
rs536054317 | snp | C/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51281438 | TTTCTCTATTCTCTC[C/T]TTTGTCACTTGGTTT | 51096 |
rs536175810 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | UTP18 | GRCh38.p7 | 17:51282585 | AATGGCCCTTGGCCC[A/T]GGTAGAGAGAGAGTC | 51096 |
rs536240319 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51276045 | ATTTTTATTTAAGGA[C/T]CAGACATTTGCAACC | 51096 |
rs536308598 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51283923 | CCTGGCCATCTCATG[G/T]TGCCTTTTTTGCCAT | 51096 |