SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs536357721 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51264182 | GCTGTGACTACAGGC[A/G]TGTGCCACCACACCT | 51096 |
rs536418157 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51264769 | CTCACTGCAACCTCC[A/G]CCTCCCAGGTTCAAG | 51096 |
rs536427175 | snp | C/T | | | intron-variant, utr-variant-3-prime | UTP18 | GRCh38.p7 | 17:51288851 | AACCTTCTAAGAGTC[C/T]TCTTCTAGTAGAGTC | 51096 |
rs536433077 | snp | A/C | | | intron-variant, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51262465 | GTATATTTATTTTTT[A/C]CTTATTTAGAGATAC | 51096 |
rs536480855 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | UTP18, MBTD1 | GRCh38.p7 | 17:51259287 | AACCCTTTTAAATAT[A/G]CAGCCTTGGAGGCTG | 51096 |
rs536523062 | snp | A/G | | | upstream-variant-2KB, intron-variant | UTP18, MBTD1 | GRCh38.p7 | 17:51259615 | GGTGGAGGAGATGGA[A/G]AGAACCCCAACGAGT | 51096 |
rs536633024 | snp | A/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51264522 | TGCCAGACTGCATGC[A/T]ATGGGGCTCTACCAG | 51096 |
rs536643437 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51291414 | TTCCCCTCCTTTTCC[C/T]GATATTCCAAGTCAG | 51096 |
rs536646398 | in-del | -/T | 0.00279162 | 0.0372561 | intron-variant, utr-variant-3-prime | UTP18 | GRCh38.p7 | 17:51289186 | CCTTGTAAGCAGACC[-/T]TTCTGTTTTTTTTGT | 51096 |
rs536744056 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UTP18 | GRCh38.p7 | 17:51271291 | ATACGTATATTAAAT[A/G]TCTTCCACCTATTTT | 51096 |
rs536765648 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51292997 | AATTTTATGATAGTA[A/G]AATATATGTGGTATG | 51096 |
rs536772622 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51284468 | CCGTGTTCTGGATCC[A/G]TTCATTTTTCACTTC | 51096 |
rs536893234 | snp | C/T | 0 | 0 | intron-variant | UTP18 | GRCh38.p7 | 17:51271777 | AGTTCAAATGATTCT[C/T]CTGCCTCAGCCACCC | 51096 |
rs536901886 | snp | A/G | 0.00279162 | 0.0372561 | downstream-variant-500B | UTP18 | GRCh38.p7 | 17:51298092 | AACCCTGATGCATAG[A/G]TCTCTTCCTGAATAG | 51096 |
rs536948132 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UTP18, MBTD1 | GRCh38.p7 | 17:51259631 | AGAACCCCAACGAGT[C/T]CAAGGCTGACGGGGT | 51096 |
rs536959994 | snp | A/C | 8.37781e-05 | 0.00647163 | missense | UTP18 | GRCh38.p7 | 17:51266197 | GGTTGACATGATGAA[A/C]AATCGGTTTCGGAAG | 51096 |
rs536986722 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UTP18 | GRCh38.p7 | 17:51290897 | AATTCCTTATAATGA[C/T]CTAGACGGTTTTGTC | 51096 |
rs537009215 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | UTP18 | GRCh38.p7 | 17:51295664 | GTTCTTTTGGCTTAG[G/T]ATTGACTTGGCTATG | 51096 |
rs537172510 | snp | A/C | | | intron-variant | UTP18 | GRCh38.p7 | 17:51265300 | TGGAGTTTTGCTCTT[A/C]TTGCCTGGGCTAGAG | 51096 |
rs537226755 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51293528 | TTTTAAGCTCATCAC[C/T]TGTCGTTAGTGTTAG | 51096 |
rs537235406 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UTP18 | GRCh38.p7 | 17:51277972 | GTTGGCGTATGGCAC[A/G]GCTCACTGGTGCTCT | 51096 |
rs537287607 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51279054 | CAGATTTTTGTAACT[C/T]CTTTTTCTCTAATTA | 51096 |
rs537427481 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51272854 | TTCTTAGCTGTCTCC[A/G]CTGGAATCATCAGTC | 51096 |
rs537433746 | snp | A/G | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | UTP18, MBTD1 | GRCh38.p7 | 17:51259752 | GGGAGCGGGGTCAGG[A/G]AGCTGCGGGGTTCCT | 51096 |
rs537491207 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UTP18 | GRCh38.p7 | 17:51273710 | CACTGTACTTTAGCC[C/T]GGGTGAAAGCGAGAC | 51096 |
rs537645178 | snp | A/G | 1.85334e-05 | 0.00304407 | synonymous-codon, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51260638 | GAGAACCGGAGCGAA[A/G]CCGAAGCGGAAGCCC | 51096 |
rs537838040 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51295889 | ATTTTGAGAATGTCA[A/C]ATTGAGAAAAAGCCA | 51096 |
rs537886645 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51281068 | CTGTAATCCCAGCTA[C/G]TTGGGAGGCTGAGGC | 51096 |
rs537895521 | in-del | -/A | 0.00199481 | 0.0315187 | intron-variant | UTP18 | GRCh38.p7 | 17:51275653 | TATTTGAAAGATGGT[-/A]AAAATGGATTCTTTT | 51096 |
rs537948225 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51274564 | CTCCTGCCTCAGCCA[C/T]GCAAGTAGCTGGGAT | 51096 |
rs538020214 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51275309 | CAAGGGGAAACCTGT[A/G]AAAACAAAATAAATA | 51096 |
rs538074475 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UTP18 | GRCh38.p7 | 17:51269066 | CCGAGGCGGGTGGAT[C/T]GCTTGAGTCCAGGAG | 51096 |
rs538103924 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51281375 | GTAAATCATTCTCCT[A/G]TGATTCCCCATGCTA | 51096 |
rs538136283 | snp | G/T | 1.65663e-05 | 0.002878 | missense | UTP18 | GRCh38.p7 | 17:51263296 | AACATGAAGACTCGG[G/T]TGACTCAGAAGTGGA | 51096 |
rs538156038 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant, downstream-variant-500B | UTP18 | GRCh38.p7 | 17:51287083 | GGGCAAGAAAAACTG[A/C]GCAGAAATGATCTTC | 51096 |
rs538157857 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51294873 | GCACCTGTTGTTTCC[A/T]GACTTTTTAATGATC | 51096 |
rs538487900 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UTP18 | GRCh38.p7 | 17:51283147 | GTGCTAGGATTACAG[A/G]CGTGAGCCACCGCGC | 51096 |
rs538558612 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UTP18 | GRCh38.p7 | 17:51276690 | TGTAACCATTCAGTC[C/G]TGCAGGTGCTTCACA | 51096 |
rs538716612 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UTP18, MBTD1 | GRCh38.p7 | 17:51259397 | GCCTCGCGGCACTGC[C/T]CCCAAGGCAGATAGA | 51096 |
rs538719969 | in-del | -/CT | | | intron-variant | UTP18 | GRCh38.p7 | 17:51267964 | AATTAAAACAACTCT[-/CT]TTGCCCTCTTCCAGG | 51096 |
rs538725825 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | UTP18 | GRCh38.p7 | 17:51274224 | GGCTAGCTCATTCTT[-/A]ACCTTTCTGCTCAAA | 51096 |
rs538808452 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51282681 | TTTGATATATGAATT[A/G]GACGCAGATATAATG | 51096 |
rs538813389 | in-del | -/CCTGCCTCGGC | 0.00159617 | 0.0282053 | intron-variant | UTP18 | GRCh38.p7 | 17:51283113 | AGCTCAGGCAACCCA[-/CCTGCCTCGGC]CTCCCAAAGTGCTAG | 51096 |
rs538876214 | snp | A/C | | | intron-variant | UTP18 | GRCh38.p7 | 17:51286333 | TAATTCTGTAACTTC[A/C]AGAAGTAGGTTTTTG | 51096 |
rs538899566 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51293614 | AAAAGATTGGACACC[C/G/T]CTGTCCACCATTGGA | 51096 |
rs538999175 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51261288 | CTTGTGATTCAGGAA[C/T]TCGATTTCGTTGATG | 51096 |
rs539053264 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | UTP18 | GRCh38.p7 | 17:51293132 | TGTGATCAGATTTTA[G/T]TATTCTTTACTGTGG | 51096 |
rs539122571 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51278908 | CTGAAATAATATTGG[G/T]GAGCATGAGTCCAAG | 51096 |
rs539161182 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51280916 | GGCGCGGTAGCTTAC[A/G/T]CCTGTAATCCCAGCA | 51096 |
rs539214309 | snp | C/T | 1.67416e-05 | 0.00289318 | missense | UTP18 | GRCh38.p7 | 17:51266247 | GTGAAAGTAAACTTT[C/T]GAAAGACAACCTTAA | 51096 |
rs539271224 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UTP18 | GRCh38.p7 | 17:51296619 | CTAAGACCCAAAGGC[C/G]ATTAGATTTTCCACC | 51096 |
rs539275747 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UTP18 | GRCh38.p7 | 17:51266638 | CTTTGTGTATTTGGG[G/T]GATGTGTGTGCTTTC | 51096 |
rs539338182 | snp | C/G | 4.06545e-05 | 0.00450839 | synonymous-codon, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51260842 | GGAGGACAAACCGGC[C/G]GTGGAGCGGTGCTTG | 51096 |
rs539354708 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51292274 | CTTTAGAAGTGAAGT[A/C]CAAATTGGGGTACTG | 51096 |
rs539354776 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51284121 | TTCAGTTTTCCCAAA[A/T]GTGTTTTACTACTGC | 51096 |
rs539621797 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UTP18 | GRCh38.p7 | 17:51284523 | TTTGGTATCTAAATC[A/G]CTAACCTTGCCTATT | 51096 |
rs539623586 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51279553 | AGATTCCTGTCCATC[A/G]TGAGCTGCTTAGTAA | 51096 |
rs539785811 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51268109 | CTGCCTCCCGGGTTC[A/T]CACCATTCTCCTGCC | 51096 |
rs539830192 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51274717 | TCAGCTCCCAACGTG[C/T]TGGGATTACAGGCGT | 51096 |
rs539871013 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51261892 | TCTTTTTGGGAAGTA[C/T]AGAACTATTACTGGA | 51096 |
rs539893168 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51268599 | AATAATTAACAAAAA[A/G]TATGTATCCAGGACT | 51096 |
rs540015915 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51294649 | ATTGTGAATAGTGCC[A/G]CATCAATAAACATAC | 51096 |
rs540093460 | in-del | -/TTTG | | | intron-variant | UTP18 | GRCh38.p7 | 17:51274437 | GTGACATAGATATCT[-/TTTG]TTTGTTTGTTTGTTT | 51096 |
rs540169864 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51278056 | AACCATTTTTCTACT[A/G]GTGGTTGAAAGTGGA | 51096 |
rs540206818 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UTP18 | GRCh38.p7 | 17:51268269 | CTGACCTCGTGATCC[A/G]CCCGCCTTGGCCTCC | 51096 |
rs540285972 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | UTP18 | GRCh38.p7 | 17:51275667 | TAAAAATGGATTCTT[C/T]TGTGGTAAAGTGACT | 51096 |
rs540291767 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51282748 | TTATCATAAGGTCCT[A/C]AGAAAGCAGGGAAGG | 51096 |
rs540424243 | snp | A/G | 0.000103466 | 0.00719183 | missense | UTP18 | GRCh38.p7 | 17:51280037 | GTGAGGAGCTTTGAA[A/G]TCTCCCCAGATGGGT | 51096 |
rs540426381 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant, downstream-variant-500B | UTP18 | GRCh38.p7 | 17:51287141 | TGCCCTCTCTTTTTT[G/T]TATCACTTTTTATTA | 51096 |
rs540490931 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51280783 | GGGCCACTGCACTCT[A/T]GCCTGGGGGACAGAA | 51096 |
rs540545291 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UTP18 | GRCh38.p7 | 17:51296026 | TGTTTCTTTCCCTGT[A/G]GCTGTAAGCTGTAAA | 51096 |
rs540608141 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant, downstream-variant-500B | UTP18 | GRCh38.p7 | 17:51289203 | TCTGTTTTTTTTGTT[C/T]TTTTTTTTTTTGAGA | 51096 |
rs540679260 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | UTP18 | GRCh38.p7 | 17:51298173 | TAGTCTCTTGAGCTA[C/T]GGAGGTCAGTCGGCT | 51096 |
rs540739658 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51290986 | AAATTCCTGTTACAT[C/T]GACAATTTTGGATAT | 51096 |
rs540913277 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UTP18 | GRCh38.p7 | 17:51264402 | TATCACCTCTTTATG[C/T]ATAAACCTTTCTTTA | 51096 |
rs540996383 | snp | C/T | 0.0023933 | 0.0345097 | upstream-variant-2KB, intron-variant | UTP18, MBTD1 | GRCh38.p7 | 17:51259446 | AACGAAACTGTGCTC[C/T]CCCTCCCCGCCAAGA | 51096 |
rs541018821 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51292994 | GGCAATTTTATGATA[A/G]TAGAATATATGTGGT | 51096 |
rs541073368 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime, intron-variant, nc-transcript-variant | UTP18, MBTD1 | GRCh38.p7 | 17:51260021 | TTTCCCCCCTTTAAC[G/T]CGGGTGGCCCCAGGA | 51096 |
rs541145551 | snp | C/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51269853 | ATTGTGTGTGTGTGT[C/G]TGTGTGTGTGTGTGT | 51096 |
rs541153840 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51291655 | CAGAAGAATTGCTTG[C/T]CCCCAAGAGGCGGAG | 51096 |
rs541219519 | in-del | -/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51284385 | AGCTTGTGTTTAGCC[-/T]TTTTTTTTTAATCAT | 51096 |
rs541324725 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51264935 | TGACCTGTTTGCCTC[A/G]GCCTCCTAAAGTGCT | 51096 |
rs541362240 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51297578 | TCTCCTCAGAGATTA[A/G]TGAATGTTGAGGGAC | 51096 |
rs541377065 | snp | A/C | | | intron-variant | UTP18 | GRCh38.p7 | 17:51263178 | TCAGAGAGTGGTAGA[A/C]AAAACATTCTATGAG | 51096 |
rs541420089 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UTP18 | GRCh38.p7 | 17:51272066 | ATCTTGTCTTTCATT[C/T]TTAAATATATTAAAC | 51096 |
rs541423003 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51279159 | GTTAAAAATCTACTA[G/T]GTAGAAATGAATGGA | 51096 |
rs541638372 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UTP18 | GRCh38.p7 | 17:51284211 | ATTCACTGAATTCTC[A/G]TTGGGAGAATAAGAG | 51096 |
rs541702808 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51277632 | GAAGACCTGGATTCC[A/G]TTTCTTTGGACAAAC | 51096 |
rs541729912 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51284965 | ACTCGGGAGGCTGAG[A/G]CAGGAAAATCACTTG | 51096 |
rs541733938 | snp | C/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51293428 | TGTACATCAATCTTG[C/T]CCAACCCACGGCGCA | 51096 |
rs541804454 | snp | A/T | 3.73734e-05 | 0.00432265 | intron-variant | UTP18 | GRCh38.p7 | 17:51266144 | ATTTATATTAACTCT[A/T]TAAAAGTTATTTAAA | 51096 |
rs541828794 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51294588 | CCACATTTTCTTAAT[C/T]CAGTCTATCATTGTT | 51096 |
rs542076460 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51293250 | TGGATGCTGTACTGA[C/T]GCTTTTTTCTCTTTC | 51096 |
rs542077827 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51266082 | TAAAAATCTTGACCT[A/G]TATTGTTTCATTAAA | 51096 |
rs542167907 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51261967 | AGTGTACGGAGGTGG[A/G]AGCTGTTGGGTTTGA | 51096 |
rs542306687 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51263549 | GATCCCACCACCGAG[A/G]GAGAACTGCTGTTAG | 51096 |
rs542343405 | snp | A/T | 0.00795532 | 0.062565 | intron-variant | UTP18 | GRCh38.p7 | 17:51280822 | CATCTCAATAAAAAA[A/T]TTTTTTTTTTAGCCA | 51096 |
rs542392960 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UTP18 | GRCh38.p7 | 17:51287381 | GTCACTGCAGCAATA[A/G]GCAGGCATCAGGTAA | 51096 |
rs542404590 | snp | C/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51290055 | CTCCTTAACTTGTAT[C/G]ATGTAGAGCAGTGTC | 51096 |
rs542455775 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51261460 | CTTTCTGGCAATGGC[A/G]AACCCTGCGTGATTG | 51096 |
rs542590282 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51276384 | TCTTCCACTGAATAT[A/G]AAAGTTCAGTAAAAT | 51096 |
rs542594850 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51263000 | ACTCATCTTTTGTTC[G/T]TGTCTTACTTGGTGT | 51096 |
rs542636248 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51264326 | GCTGAGATTACAGGC[A/G]TGAACTGCTGTGCCC | 51096 |
rs542672246 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51276873 | GAGCTTCCGTGCCTT[C/T]TCAGGGCACGCCACC | 51096 |
rs542735757 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51270496 | TTATGCTAGCTGTTG[A/C]AACAAAATCCCACAG | 51096 |
rs542906379 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51290097 | TGGTATATATATTGG[G/T]ATTCTGCATATGATT | 51096 |
rs542968088 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51268773 | CGTATATGCTTTAAA[C/T]GTATCAAGCTTTATG | 51096 |
rs543007573 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | UTP18 | GRCh38.p7 | 17:51291835 | GAAAACCAGCTCCCC[A/C/G]AACTTCAAAGTCATT | 51096 |
rs543039853 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51281680 | TCAGTGTCACTATCC[C/T]GGTTGTAATGTTGTC | 51096 |
rs543048904 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | UTP18 | GRCh38.p7 | 17:51279467 | GTCCTTAAGTAAACT[C/G]ACATATTGTGAAAAG | 51096 |
rs543055264 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UTP18 | GRCh38.p7 | 17:51296075 | AGATAACCAAAACTT[A/T]TATGCGCTGTCCAGG | 51096 |
rs543106348 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51284255 | GTGAACTTTAGAGCA[A/G]TATCCTGCAAGGAAG | 51096 |
rs543163394 | snp | C/G | | | missense, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51260640 | GAACCGGAGCGAAGC[C/G]GAAGCGGAAGCCCGG | 51096 |
rs543165981 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51277672 | TCTCTGATCTTCAGG[A/C]AACTTGGATACTCTG | 51096 |
rs543197274 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | UTP18 | GRCh38.p7 | 17:51289266 | CAGTGGTGTGATCTC[A/G]GCTCACTGCAGCCTC | 51096 |
rs543236767 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51297117 | CCCCTAAGTTACTGC[A/G]TCTTTATTTAGAGGG | 51096 |
rs543239370 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51265031 | GTCTATTGGAGACTT[C/T]TTAAATAATCTTGGT | 51096 |
rs543258244 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51282160 | GGAGACTTTCAAGTG[C/G]TTCTGCTCTGTGGGT | 51096 |
rs543302617 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UTP18, MBTD1 | GRCh38.p7 | 17:51259523 | AAGTCTCGGATCCAG[C/T]CTTTCCCCCCTAGCC | 51096 |
rs543338568 | in-del | -/AG | 0.00119737 | 0.0244387 | intron-variant | UTP18 | GRCh38.p7 | 17:51290456 | TGGTTTGCTGGAAAA[-/AG]AGTGTGAAAATTACA | 51096 |
rs543342243 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51291147 | GCCTGTAATCCCAGC[A/G]CTTTGTGAGGCCGAG | 51096 |
rs543452075 | snp | A/G | | | intron-variant, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51260959 | GCGCGGGCTGGGCGC[A/G]CTCGGGCGGGGCGCG | 51096 |
rs543520758 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51284749 | GCAGTTTTCTTTTGT[A/G]TATGTGAATGTATAC | 51096 |
rs543565735 | snp | C/G | | | intron-variant, downstream-variant-500B | UTP18 | GRCh38.p7 | 17:51286987 | CCCCCTTCCCCCCCC[C/G]ACCCACAGGCCCCGG | 51096 |
rs543657536 | snp | G/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51267331 | CTGACATTTTAAGAC[G/T]CCTGTTTTTTATTGA | 51096 |
rs543711801 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UTP18, MBTD1 | GRCh38.p7 | 17:51259761 | GTCAGGGAGCTGCGG[A/G]GTTCCTGGGGTCGGA | 51096 |
rs543797844 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51283796 | ATTTTTGTATTTTTA[A/G]TAGAGATGGTGATTC | 51096 |
rs543798574 | snp | A/G | | | intron-variant, downstream-variant-500B | UTP18 | GRCh38.p7 | 17:51286875 | GTACATGTGCATAAC[A/G]TGCAGGTTTGTTACA | 51096 |
rs543824658 | snp | A/G | 7.37273e-05 | 0.0060711 | intron-variant, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51260935 | CCCGAGGGTGAGGGA[A/G]GCCGCGGCGCGCGGG | 51096 |
rs543831187 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | UTP18 | GRCh38.p7 | 17:51291963 | CCCTTGTAGCAAATG[-/T]TTTTTTTCCTGATCA | 51096 |
rs543844526 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UTP18 | GRCh38.p7 | 17:51267743 | CTTTTTCTCAGCTTT[G/T]TGTCAGGGTCTTATA | 51096 |
rs543905961 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UTP18 | GRCh38.p7 | 17:51268248 | AGCCAGGATGGTCTC[A/G]ATCTCCTGACCTCGT | 51096 |
rs543973668 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UTP18 | GRCh38.p7 | 17:51278289 | GAGTCTGCATTTCTG[A/G]TTCTCTCAGGTGATG | 51096 |
rs544045636 | snp | C/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51281926 | CATCAGCCCTTGTAG[C/G]AATACTCTCTTGACT | 51096 |
rs544070689 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51272122 | GTGTTTTTTTGAGAC[A/G]GAGTCTTATTCTGTT | 51096 |
rs544128867 | snp | A/C | 0 | 0 | intron-variant | UTP18 | GRCh38.p7 | 17:51266367 | TTCTTGTGTAGTTTT[A/C]CATTTTGAAACAGTA | 51096 |
rs544129362 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51272513 | GTCAATATTTGCCTG[C/G]TTATATTTCATTGAG | 51096 |
rs544171187 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51273220 | GTTTTGCTTTTGCCA[A/G]TTGCAGCTTTAAAAA | 51096 |
rs544188992 | snp | A/C | 0.000399281 | 0.0141238 | missense | UTP18 | GRCh38.p7 | 17:51288180 | GCAATTGCTTCAGAA[A/C]AAATGAAAGAAGCAG | 51096 |
rs544249666 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | UTP18 | GRCh38.p7 | 17:51289107 | CCATATCATTTAGGG[A/T]AAGTTTCATGCCAGT | 51096 |
rs544274587 | in-del | -/T | 0.00358779 | 0.0422022 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | UTP18, MBTD1 | GRCh38.p7 | 17:51259189 | GCTTTGGATGACCTC[-/T]TAATGTCTCTTCCGA | 51096 |
rs544364736 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51262120 | TTAGACTCGCCCTGT[C/T]GCCCAGGCTGGAGTG | 51096 |
rs544401315 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51283263 | AGCCTCTGCCTCCTG[A/G]GTTCCAGCAATTCTC | 51096 |
rs544469325 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51294671 | TAAACATACATGTGC[A/G]TGTGTCTTTATAGCA | 51096 |
rs544729869 | snp | C/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51274698 | CTCAGGTGATCTGCC[C/T]GCCTCAGCTCCCAAC | 51096 |
rs544741831 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51297327 | GAGATGGGTCTTCAG[A/G]TATAGCTATAGCTTG | 51096 |
rs544765899 | in-del | -/TT | | | intron-variant | UTP18 | GRCh38.p7 | 17:51282868 | TTCTTCTTCTTCTTC[-/TT]TTTTTTTTTTTTTTT | 51096 |
rs544821724 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, utr-variant-5-prime | UTP18, MBTD1 | GRCh38.p7 | 17:51260290 | TAGTCGGGGTTTCTT[A/G]CGCTCCTTTCAATAT | 51096 |
rs544986534 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51264300 | ATACACCCGTCTCTG[C/T]CTCCCAAAGTGCTGA | 51096 |
rs545022503 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | UTP18 | GRCh38.p7 | 17:51279042 | GGGTCCTTAACCAGA[-/T]TTTTTGTAACTCCTT | 51096 |
rs545042977 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51265100 | TATGTTAGATTTATT[A/G]TAGGTTTTCCCCAGC | 51096 |
rs545051685 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UTP18 | GRCh38.p7 | 17:51270605 | TAGGGACCCAAGTTT[A/G]TAGAAGTTCTGTCAT | 51096 |
rs545101763 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | UTP18 | GRCh38.p7 | 17:51265602 | ACAGTCTCACTCTTT[C/T]GCCCAGGCTGGAGTA | 51096 |
rs545113496 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | UTP18 | GRCh38.p7 | 17:51298149 | TGCTTTAGGGGATCA[A/G]CTAACAGGTAGTCTC | 51096 |
rs545151191 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UTP18 | GRCh38.p7 | 17:51290374 | TGAGCCAAGATCGTG[C/T]CTCTGTACTCCAGCC | 51096 |
rs545224834 | snp | C/T | | | intron-variant, downstream-variant-500B | UTP18 | GRCh38.p7 | 17:51289479 | CCCAAAGTGCTGGGA[C/T]TACAGGAGTGAGCCG | 51096 |
rs545265582 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51269342 | CCAAAAAAATCTGTT[C/T]TTTGACTGTAGGTTT | 51096 |
rs545325490 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51263619 | ATACAGTAGCTAAGA[G/T]AATACAGTGTTTGAA | 51096 |
rs545330840 | snp | A/C | | | intron-variant | UTP18 | GRCh38.p7 | 17:51297236 | GAGGTCTGATCTCTA[A/C]TGTTGCATTCAATAA | 51096 |
rs545367018 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UTP18 | GRCh38.p7 | 17:51277589 | GTTAGCAGTTGATGC[A/C]GCAGAAAAAGCATGA | 51096 |
rs545391497 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51284865 | CAAGAGTTCGAGACC[A/G]GCCTGGCCAACATGG | 51096 |
rs545393961 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51276883 | GCCTTCTCAGGGCAC[A/G]CCACCTCCTCAGCAC | 51096 |
rs545446305 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UTP18 | GRCh38.p7 | 17:51285438 | TTGAGGAATTGAATA[A/T]ACTAGGTGGTGCATG | 51096 |
rs545539101 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51278419 | ATGTCATTTCACTAT[A/T]CAAAAGTAATGGATT | 51096 |
rs545560015 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, utr-variant-5-prime, intron-variant, nc-transcript-variant | UTP18, MBTD1 | GRCh38.p7 | 17:51259921 | CCTCCCCGGGCTGGG[A/G]GCAGGTGCCTCTCCC | 51096 |
rs545582422 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51296860 | AATGATTGTGATTAC[A/G]TATTTTTCCCACTAA | 51096 |
rs545582987 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UTP18 | GRCh38.p7 | 17:51274970 | TGGGAGGCCGAGGCG[A/G]GCAGATCACCTGAGG | 51096 |
rs545607524 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | UTP18 | GRCh38.p7 | 17:51282921 | TTGCTTAGGCTGGAG[G/T]GCAGTGGCACGATCT | 51096 |
rs545607587 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UTP18 | GRCh38.p7 | 17:51290917 | ACGGTTTTGTCATCC[C/T]ATTACAAAGCACTGT | 51096 |
rs545664383 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51291946 | GAACAGCTTTGTCCT[A/C]ACCCCTTGTAGCAAA | 51096 |
rs545668836 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51283492 | ATTCTGTATGGAGTC[A/G]TTTGTGTGATTAGTA | 51096 |
rs545717781 | snp | C/T | | | intron-variant, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51261515 | CTATCCCTTTAAATT[C/T]TATACCAGGCTTTTC | 51096 |
rs545727514 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51292564 | AAAATCACTTTGATG[A/G]TATAAAGTCTGACCT | 51096 |
rs545794991 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UTP18 | GRCh38.p7 | 17:51277462 | GCTTTTGAGATAACA[C/T]GTTTGAATGAAACCA | 51096 |
rs546015364 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51294463 | TGTTTGGTTTTTTGC[C/T]CTTGTGATAGTTTGC | 51096 |
rs546170591 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51261713 | AGGACATTCGGGAAA[A/G]GGAGATGGGCGTGTG | 51096 |
rs546186591 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51261426 | CAAATATTGGTGAAC[C/G]TGTTAGTTGCCAGAT | 51096 |
rs546334945 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | UTP18 | GRCh38.p7 | 17:51286837 | GTTTTTAAATTTTTT[C/T]TATTATACTTTTAAG | 51096 |
rs546347545 | snp | C/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51270974 | ACTAGCACTCAGCTT[C/T]ATGATTATCTCCAGT | 51096 |
rs546354214 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, missense | UTP18 | GRCh38.p7 | 17:51286513 | ACTGCTTGTATATAT[A/G]TCCCTACCACCGTTT | 51096 |
rs546357224 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51272567 | TAATGTAGATTAATT[A/G]GATCTAGGATGATGG | 51096 |
rs546410495 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51273569 | AATATGTTTGCTGTC[A/G]TTTTGCCCTGGTAAA | 51096 |
rs546422145 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UTP18 | GRCh38.p7 | 17:51294761 | TTTCTAGTTCTAGAT[C/T]CCTGAGGAATCGCCA | 51096 |
rs546584443 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UTP18 | GRCh38.p7 | 17:51275137 | AACAGGCAGAGGTTG[C/T]GGTGAGTCGAGATTA | 51096 |
rs546596624 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UTP18 | GRCh38.p7 | 17:51294112 | CAGTATGAAGAGATA[C/T]TATATATTCCTAATT | 51096 |
rs546657380 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51294231 | TACTTTAAGTTTTAG[A/G]GTACATGTGTGCACT | 51096 |
rs546660282 | snp | C/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51269024 | TGGCTCGGTAGCTCA[C/G]GCCTGTCATCCCAGT | 51096 |
rs546735933 | snp | A/T | | | synonymous-codon | UTP18 | GRCh38.p7 | 17:51288149 | TCTGACCTTCAATCC[A/T]ACTACAGAAATCTTG | 51096 |
rs546737012 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UTP18 | GRCh38.p7 | 17:51269014 | ATTTCTTGCCTGGCT[C/T]GGTAGCTCACGCCTG | 51096 |
rs546767038 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | UTP18 | GRCh38.p7 | 17:51272743 | GTAGCCCTTTGTGGC[C/T]GCAATCCAAAATCTG | 51096 |
rs546796643 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51287617 | CCACCCCCACAAACC[C/T]TTAGGAATGCAGTGC | 51096 |
rs546971294 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51268347 | CCAGTTCTTACGAAC[A/G]CAGCTATCATGCTTC | 51096 |
rs547165550 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UTP18 | GRCh38.p7 | 17:51291875 | TTGGTGAGTGAATGC[C/T]TGAGGCCTAGTTTCA | 51096 |
rs547296734 | in-del | -/TACC | 0.000798881 | 0.01997 | intron-variant | UTP18 | GRCh38.p7 | 17:51292725 | AGGTAACTGCTTCCA[-/TACC]TGGGTTTTATTCATC | 51096 |
rs547306607 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UTP18 | GRCh38.p7 | 17:51268327 | CATGGCGCCCGGCCC[A/G]GGTACCAGTTCTTAC | 51096 |
rs547308017 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51274474 | TGAGACAGAGTTTTG[C/T]TCTTTTGCTCAGGCT | 51096 |
rs547362110 | snp | G/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51280515 | AAGCTAAGGATATTT[G/T]TACATTTTAAATTTT | 51096 |
rs547371082 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | UTP18, MBTD1 | GRCh38.p7 | 17:51259610 | CAAAGGGTGGAGGAG[A/G]TGGAGAGAACCCCAA | 51096 |
rs547487912 | snp | A/G | 6.64055e-05 | 0.0057618 | missense | UTP18 | GRCh38.p7 | 17:51275912 | GTCCTACTGTTGCTC[A/G]GATCTCATCTGTGCA | 51096 |
rs547517139 | in-del | -/AATA | 0.00597247 | 0.0543191 | intron-variant | UTP18 | GRCh38.p7 | 17:51276344 | ACAAGGAACCATAAT[-/AATA]GGGGATTTGGAGTAA | 51096 |
rs547551347 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51276550 | TACTGGGTCTTCCAT[A/G]TTTAATCTAACACTG | 51096 |
rs547552901 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UTP18 | GRCh38.p7 | 17:51263701 | CAGTTTGGAACCTAC[A/G]TTTTTTCCTTTGTGA | 51096 |
rs547590582 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UTP18 | GRCh38.p7 | 17:51295676 | TAGGATTGACTTGGC[G/T]ATGCGGGCTCTTTTT | 51096 |
rs547668685 | in-del | -/GA | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | UTP18, MBTD1 | GRCh38.p7 | 17:51258970 | GGGTGAGGAGGATGT[-/GA]GAGAAAATTTGAGAA | 51096 |
rs547684915 | snp | A/G | | | intron-variant, utr-variant-3-prime | UTP18 | GRCh38.p7 | 17:51288722 | GGCTAACGAGAGATG[A/G]CTTCCAGGACTCTGC | 51096 |
rs547707457 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | UTP18, MBTD1 | GRCh38.p7 | 17:51259179 | AGGGGACGGCTGCTT[C/T]GGATGACCTCTAATG | 51096 |
rs547733292 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51264745 | TGGAGTTCAGTGGCG[C/T]GATCTTGGCTCACTG | 51096 |
rs547875698 | snp | C/T | 1.76052e-05 | 0.00296686 | intron-variant | UTP18 | GRCh38.p7 | 17:51266163 | AAGTTATTTAAAATA[C/T]GCTGTTCTGTTTTTG | 51096 |
rs547915308 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UTP18 | GRCh38.p7 | 17:51292118 | TGCCTTCCCAAATTA[A/G]ATGTAAATAAATTTT | 51096 |
rs547945797 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51267836 | AGGGATCACAGTCCT[A/G]TGCTGTCATCCAGTT | 51096 |
rs548214529 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51292615 | ACTGCCCAGCTGAAT[A/G/T]ATAACGGTTGTATAT | 51096 |
rs548282792 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, synonymous-codon | UTP18 | GRCh38.p7 | 17:51286681 | CCCATACCCGTGCCA[A/G]CCCTGTAGCGAGGGA | 51096 |
rs548290009 | snp | A/G | 0.000152505 | 0.00873093 | synonymous-codon, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51260755 | CCGGCCGAGCGCGGC[A/G]GCCGCTGCGATTGCA | 51096 |
rs548373508 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51284463 | AATTCCCGTGTTCTG[C/G]ATCCGTTCATTTTTC | 51096 |
rs548478534 | snp | C/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51267280 | TACCTATCTTTTAAG[C/T]GTTCAGACCTGTTGT | 51096 |
rs548479922 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51261060 | GGAGCCCGAGAACGC[G/T]GGCGCGGAGGGTCGC | 51096 |
rs548493068 | in-del | -/TT | 0.00279162 | 0.0372561 | intron-variant | UTP18 | GRCh38.p7 | 17:51293015 | TATATGTGGTATGAC[-/TT]TGCCTAGGCTTCAGT | 51096 |
rs548502918 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51292983 | AAGTACAAAATGGCA[A/G]TTTTATGATAGTAGA | 51096 |
rs548538478 | snp | C/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51268428 | ATATATAATGAAGTT[C/T]TGTATATTCTTAACA | 51096 |
rs548591401 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51279494 | AAAGTTTTGGGGTTT[G/T]TTTTGTTTTTTGTTT | 51096 |
rs548711924 | snp | C/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51282826 | TTGATGGTTCTCTTC[C/G]TCTCTCTCCGCTTCT | 51096 |
rs548715412 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UTP18 | GRCh38.p7 | 17:51273601 | ACTTATGTTATTGTT[C/T]TTTTTTTTTCCTTTT | 51096 |
rs548893575 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51285935 | ACCTTATATCATTGT[A/G]TTTTTTCCTATTTAA | 51096 |
rs549005019 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51294818 | GTTTACAGTCCCACC[A/G]ACAGTGTAAAAGTGT | 51096 |
rs549033006 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51262355 | TCCCAAAGTGCTGAG[A/G]CTACAAGTGTGAGCC | 51096 |
rs549068372 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | UTP18 | GRCh38.p7 | 17:51295415 | TTTCAGCTTTCTACA[C/T]ATGGCTAGCCAGTTT | 51096 |
rs549088284 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51281050 | AGGCATGCTGGCGCT[C/T]GCCTGTAATCCCAGC | 51096 |
rs549147367 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UTP18 | GRCh38.p7 | 17:51263901 | TTGACTTTTTCTACA[G/T]AAAGTTACTTTGTAA | 51096 |
rs549198634 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51261749 | GCCTGTGAAATTTTA[A/G]ATAAAGGGGGCAGAG | 51096 |
rs549216111 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51275246 | AAATTTAACTTGGTG[G/T]TTACAAACAAAACAC | 51096 |
rs549279279 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51269043 | TGTCATCCCAGTGCT[C/T]TGGGAGCCCGAGGCG | 51096 |
rs549281509 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51275756 | GTTTGGTTACCATTC[C/T]AGTGCATTTTTTTCC | 51096 |
rs549502226 | snp | A/G | | | intron-variant, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51262176 | AACCTCCACTTCCTG[A/G]GTTCAAGCGATTCTC | 51096 |
rs549567172 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51297677 | TTAGCAAGGAGGGGA[A/G]AGCAGTTTAGCTCTC | 51096 |
rs549742674 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51283734 | TTCTCATGCCTCAGC[C/T]TCCCCGAGTAGCTGG | 51096 |
rs549777908 | in-del | -/G | 0.00478085 | 0.0486577 | intron-variant | UTP18 | GRCh38.p7 | 17:51274065 | GGATCCTTAGCCTCA[-/G]TATCAGACCTGTTTC | 51096 |
rs549797756 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51276944 | TGAATACCTTCTGTT[A/G]AGCCTTTTTATGAAG | 51096 |
rs549831953 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51283102 | TCGAACTCCTGAGCT[A/C]AGGCAACCCACCTGC | 51096 |
rs549910267 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UTP18, MBTD1 | GRCh38.p7 | 17:51258979 | GGATGTGAGAGAAAA[C/T]TTGAGAAGTAAAAAA | 51096 |
rs549998398 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UTP18 | GRCh38.p7 | 17:51267252 | ACAGAGGTGAGCCAC[C/T]GTGCTCAGCCATTAC | 51096 |
rs550036500 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51277974 | TGGCGTATGGCACGG[C/T]TCACTGGTGCTCTCC | 51096 |
rs550095925 | snp | C/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51279876 | GACTTATTCGGGGTC[C/T]GAGCCAGGGTTTTGT | 51096 |
rs550139671 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UTP18 | GRCh38.p7 | 17:51267197 | TCTTGAACTGGGCTC[A/G]AGCGATCTGCCCTTC | 51096 |
rs550147229 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UTP18, MBTD1 | GRCh38.p7 | 17:51259657 | GGGGTGGGGGGAGGG[G/T]AACCCCTGAATCGTT | 51096 |
rs550274846 | snp | A/G | 0.0520825 | 0.152737 | intron-variant | UTP18 | GRCh38.p7 | 17:51285083 | AAAAAAAGGAAAAAA[A/G]AAAAGAAATATTCTT | 51096 |
rs550285561 | snp | A/G | 0.000341647 | 0.0130655 | missense, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51260783 | GCAGTCGCGGCGGCG[A/G]AGGAAGAGAGACGGC | 51096 |
rs550339390 | snp | C/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51263074 | TTCCATCTTGCCTCA[C/T]CTGTCCAGTCGGTGC | 51096 |
rs550406439 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51261523 | TTAAATTCTATACCA[C/G]GCTTTTCTTGAGAGA | 51096 |
rs550438179 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51265788 | AAGATGGTCTGGATC[C/T]CTTGACCTCGTGATC | 51096 |
rs550451595 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | UTP18, MBTD1 | GRCh38.p7 | 17:51260148 | TTCCACCGTGGGACC[C/T]TCTGCAGGCTCCGTA | 51096 |
rs550479237 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51272636 | ACACTAGTAATCCCA[A/G]AACGTTTTATTTTAA | 51096 |
rs550494206 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51278571 | TGCTTTGGAGACATG[A/G]CATTGATCTTTCCTT | 51096 |
rs550591240 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51261250 | CAAACTGAGGGTGGT[C/T]TTTTGATCACCTGCC | 51096 |
rs550691840 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51280899 | AAAAAAACCTAGGAC[C/G]AGGCGCGGTAGCTTA | 51096 |
rs550745361 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51278774 | TTTAGTCAGTACATA[C/T]GGTTTATTCAGAAAT | 51096 |
rs550944134 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51273711 | ACTGTACTTTAGCCC[A/G]GGTGAAAGCGAGACC | 51096 |
rs551018383 | snp | C/T | | | intron-variant, downstream-variant-500B | UTP18 | GRCh38.p7 | 17:51287160 | CACTTTTTATTAGCC[C/T]CCTTTGAAGGGCCTA | 51096 |
rs551092265 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51282464 | AAGAAAGAAGAAAAT[A/G]AAGAGAAAGAGGAAG | 51096 |
rs551111288 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51268322 | TGAGCCATGGCGCCC[A/G]GCCCAGGTACCAGTT | 51096 |
rs551139634 | in-del | -/A | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51262102 | TAGATTTTTTTTTTT[-/A]TTTTAGACTCGCCCT | 51096 |
rs551169658 | snp | G/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51284042 | ATCTTTAAAACACTT[G/T]CCTTTATTATAACAT | 51096 |
rs551286540 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51280292 | AATAAAGTTGAGTAG[G/T]TGCTAGAAAATAGAG | 51096 |
rs551368350 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51296457 | GGAAAACAGGTTATA[A/C]CAGGATAATTTCATC | 51096 |
rs551403928 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UTP18, MBTD1 | GRCh38.p7 | 17:51259067 | CAACAATTAGAACTA[C/T]TGAAATATGGGCTTT | 51096 |
rs551420421 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51279715 | GCATATATTTGGAAA[A/G]TTAGTTGATATGTTT | 51096 |
rs551461273 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, downstream-variant-500B | UTP18 | GRCh38.p7 | 17:51289434 | GGCTGGTCTCGAACT[C/T]CCGACCTCATGGTCC | 51096 |
rs551528638 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51282299 | TTTTTTAACTTTTAA[A/G]AAGGATTAATTTTAG | 51096 |
rs551580951 | snp | A/G | 1.65932e-05 | 0.00288034 | missense | UTP18 | GRCh38.p7 | 17:51268880 | GCCTGGGCAGAGACT[A/G]CTAAGCGGAAAACAT | 51096 |
rs551675603 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | UTP18 | GRCh38.p7 | 17:51264041 | CCCTTTTTTTTTTTT[A/T]AATTATTTTTTTTGA | 51096 |
rs551685458 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | UTP18 | GRCh38.p7 | 17:51294891 | CTTTTTAATGATCGC[C/G]ATTCTAACTGGTGTG | 51096 |
rs551709237 | in-del | -/C | 0.00953873 | 0.0683987 | intron-variant | UTP18 | GRCh38.p7 | 17:51293258 | TACTGACGCTTTTTT[-/C]CTCTTTCTTCCTTTT | 51096 |
rs552147566 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51277830 | AATTTATCTGCCCTC[C/T]ACCATACCCATTCTT | 51096 |
rs552220937 | snp | C/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51291706 | CACCACTGTACTCCA[C/G]CCTGGGCAACAGAGT | 51096 |
rs552301797 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51293447 | ACCCACGGCGCAGGA[C/T]GGTTTGATTGTGGCC | 51096 |
rs552340442 | snp | C/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51268534 | TACATAGTCCTGATA[C/T]CTGGGATGTGTTGAT | 51096 |
rs552418613 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51267620 | TAAGTTGGGCTTAAA[A/G]TCTTGATTAGAATTC | 51096 |
rs552570643 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UTP18 | GRCh38.p7 | 17:51285442 | GGAATTGAATATACT[A/G]GGTGGTGCATGAGTA | 51096 |
rs552672577 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51278909 | TGAAATAATATTGGG[A/G]AGCATGAGTCCAAGC | 51096 |
rs552698151 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51279563 | CCATCATGAGCTGCT[G/T]AGTAAGTGGCCAGCA | 51096 |
rs552774307 | in-del | -/T | 0.229723 | 0.249176 | intron-variant | UTP18 | GRCh38.p7 | 17:51293502 | AAACATGAGTTGTTG[-/T]TTTTTTTTTTTTTTA | 51096 |
rs552784896 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51266439 | TTTTTTAGGGGAGAG[A/G]GGACAAAACACAGAC | 51096 |
rs552786795 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | UTP18, MBTD1 | GRCh38.p7 | 17:51260216 | ATTGGGGCTTGTGTC[A/G]AGTCAAGTGGTTACA | 51096 |
rs552807860 | snp | A/G | 0.000422776 | 0.014533 | synonymous-codon, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51260851 | ACCGGCCGTGGAGCG[A/G]TGCTTGGAGGAGCTG | 51096 |
rs552888440 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51266657 | GTGTGTGCTTTCCCA[A/G]TGTATTTGAGAGTAA | 51096 |
rs552955079 | snp | A/C | | | intron-variant | UTP18 | GRCh38.p7 | 17:51295559 | GTTCCATTGGTCTAT[A/C]TCTCTGTTTTGGTAC | 51096 |
rs552957671 | snp | C/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51267905 | TAGTTGTTTATGGCT[C/T]GTGGGCTTAGTTTGG | 51096 |
rs553162183 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51280516 | AGCTAAGGATATTTT[G/T]ACATTTTAAATTTTA | 51096 |
rs553233922 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UTP18 | GRCh38.p7 | 17:51295029 | TCTGTTCATATCCTT[C/T]GCCCACTTTTTGATG | 51096 |
rs553237580 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51290001 | CCCTAGATTCTGCAC[A/G]GGGCTTTATATGGCA | 51096 |
rs553299120 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51265738 | CCAGCTAATTTCTGT[A/G]TTTTTAGTAGAGATG | 51096 |
rs553399860 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51261903 | AGTACAGAACTATTA[C/T]TGGAAACATGCTGAA | 51096 |
rs553559196 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51272351 | TGATCCACTCACCTC[A/G]GCCTCGCAAAGTGCT | 51096 |
rs553621078 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51263523 | TATAGAAAAGATCTT[C/T]CATGGTTCCTGATCC | 51096 |
rs553816455 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UTP18 | GRCh38.p7 | 17:51283328 | CACACACCACCACAT[C/T]GGCTAATTTTTGTAT | 51096 |
rs554015891 | snp | C/G/T | 0.000186411 | 0.00965249 | intron-variant | UTP18 | GRCh38.p7 | 17:51286460 | AGCATACTCTCTACT[C/G/T]TTTGTTCACTCTCTC | 51096 |
rs554018896 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | UTP18 | GRCh38.p7 | 17:51288803 | AAGCAAAATCAGCAA[A/T]GGGAAAGGGTACATG | 51096 |
rs554090897 | in-del | -/CTT | 0.00119737 | 0.0244387 | intron-variant | UTP18 | GRCh38.p7 | 17:51283170 | CACCGCGCCCAGCCA[-/CTT]CTTTTTTTTTTTTTC | 51096 |
rs554093076 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | UTP18 | GRCh38.p7 | 17:51281160 | TATATATATATATAT[A/T]TATATTTTTTTTAAA | 51096 |
rs554139735 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UTP18 | GRCh38.p7 | 17:51290825 | GGAAAGAAGCCAGGC[A/G]TAGCAGCTCCATATA | 51096 |
rs554156472 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51281653 | GATGGGAAGTTTTGT[A/G]TCTTGACTGTATCAG | 51096 |
rs554156483 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51274731 | GCTGGGATTACAGGC[A/G]TGAGCCACCGCGCCC | 51096 |
rs554249064 | snp | C/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51270086 | GTCTTGAACTCTTGG[C/G]CTTCCAAAGTGTTGG | 51096 |
rs554333256 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51277443 | GTTTGGAAAATGTCT[G/T]TGTGCTTTTGAGATA | 51096 |
rs554343781 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51264099 | TGGAGTGCAGTGGTG[C/T]GATCTTGGTTCACTG | 51096 |
rs554397709 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UTP18 | GRCh38.p7 | 17:51296694 | GACTGGAATTGACTG[A/G]TGACATTTTTATTGT | 51096 |
rs554408314 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51294279 | ATGTATACATGTGCC[A/G]TGTTGGTATGCTGCA | 51096 |
rs554503397 | in-del | -/AACTCTT | 0.00179226 | 0.0298817 | intron-variant | UTP18 | GRCh38.p7 | 17:51285218 | TAAAGCAAAATTAAC[-/AACTCTT]TTTTTCGCTCTTTTA | 51096 |
rs554534602 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | UTP18 | GRCh38.p7 | 17:51275023 | ACCAACATGGGGAAA[C/T]CTCATCTCTACTGAA | 51096 |
rs554667375 | snp | C/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51283708 | ATCCTCTGCCTCCTG[C/G]GTTCAGGCGATTCTC | 51096 |
rs554817005 | snp | G/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51265042 | ACTTTTTAAATAATC[G/T]TGGTATATTAGTTCC | 51096 |
rs554885514 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UTP18 | GRCh38.p7 | 17:51265533 | CTCCCAAAGTGCTGG[A/G]ATTGCAGGCATGAGC | 51096 |
rs554993416 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51272444 | ATAATTCCGTTGTTT[A/C]GATCCCTGTGGGGAT | 51096 |
rs554999017 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51266892 | GAGGTAGGATCTCAC[C/T]CTGTCACCCAGGCTG | 51096 |
rs555150376 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51284655 | CTTAGAAGCTTTTTC[G/T]AAAAGTTCAACTCAA | 51096 |
rs555228961 | snp | A/G | | | splice-acceptor-variant | UTP18 | GRCh38.p7 | 17:51277129 | TTGTACTTCTTTATA[A/G]GTTGATGGGAAAACA | 51096 |
rs555246165 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51261362 | ATGTCCCCATGTGAC[A/T]ATGAGACCCACCATG | 51096 |
rs555265449 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51278213 | GAAGTAAATGTGCAC[A/G]TGAATCACCTGGGGG | 51096 |
rs555287052 | in-del | -/TTTAG | 0.00398564 | 0.0444627 | intron-variant | UTP18 | GRCh38.p7 | 17:51295194 | GCTGTGCAGAAACTC[-/TTTAG]TTTAATTAGATCCCA | 51096 |
rs555328719 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51279001 | GTGGAAAGTAGCCTT[A/C]ATTTGTATTTTCCTG | 51096 |
rs555417375 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UTP18 | GRCh38.p7 | 17:51295855 | ACCTGGGGAATATAT[A/G]TATTTTTTGGAAAGC | 51096 |
rs555528947 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UTP18 | GRCh38.p7 | 17:51274503 | CTGGAGTGCAAGGGC[A/G]TGATCTCGGCTCACT | 51096 |
rs555619305 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | UTP18 | GRCh38.p7 | 17:51289055 | GTTTAGCATAAACCA[C/G]ATTGTTTGTACAAAC | 51096 |
rs555671111 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UTP18 | GRCh38.p7 | 17:51286329 | CCCATAATTCTGTAA[C/T]TTCAAGAAGTAGGTT | 51096 |
rs555740785 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UTP18 | GRCh38.p7 | 17:51294306 | TGCACCCATTAACTC[A/G]TCATTTAGCATTAGG | 51096 |
rs555808425 | snp | G/T | 3.33762e-05 | 0.00408497 | synonymous-codon | UTP18 | GRCh38.p7 | 17:51288104 | AAAGCCAATAAAAGC[G/T]ATAATGAACTTGGTT | 51096 |
rs555939365 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51264227 | TTTTTAGTAGAGACA[A/G]AGTTAGACGGAGTTT | 51096 |
rs555978868 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51262032 | CACTTGGACATTTCT[A/G]TCATTGGTTTTGGGA | 51096 |
rs556088664 | snp | C/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51281428 | CATGCCTTTTTTTCT[C/G]TATTCTCTCTTTTGT | 51096 |
rs556221653 | snp | C/T | | | intron-variant, utr-variant-3-prime | UTP18 | GRCh38.p7 | 17:51288952 | CTCATTAGAGACTCA[C/T]TGCAGAAGGTTTTTA | 51096 |
rs556239144 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | UTP18 | GRCh38.p7 | 17:51264785 | CCTCCCAGGTTCAAG[C/T]GATTCTCCTGCTTCA | 51096 |
rs556267029 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51271279 | AGATTATTAGTAATA[C/T]GTATATTAAATGTCT | 51096 |
rs556286779 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51276876 | CTTCCGTGCCTTCTC[A/C]GGGCACGCCACCTCC | 51096 |
rs556449662 | snp | A/G | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | UTP18, MBTD1 | GRCh38.p7 | 17:51259760 | GGTCAGGGAGCTGCG[A/G]GGTTCCTGGGGTCGG | 51096 |
rs556465292 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51275483 | AAAGATGCCAGGTGC[A/C]AAAGTAGAAGTTTTA | 51096 |
rs556523431 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51284022 | TTTAGTCTACTGAGA[A/G]ACTAATCTTTAAAAC | 51096 |
rs556560822 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UTP18 | GRCh38.p7 | 17:51292520 | AATAGGTGTATGTAT[C/G]AGTGGTTTTTACCCA | 51096 |
rs556588605 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51277502 | TTTACTGAACACTTA[C/G]GGAATGATCATAATT | 51096 |
rs556623138 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51293101 | ATGAACCTTCATGTT[G/T]AAAATCTCTTTTCCC | 51096 |
rs556684552 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51285390 | AAAGAGAGGTTCTTG[C/T]AACCTTAATCACATT | 51096 |
rs556698062 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UTP18 | GRCh38.p7 | 17:51271522 | TCTTATTATGTTGCC[C/T]ACATTGGTATTCAGT | 51096 |
rs556731340 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | UTP18 | GRCh38.p7 | 17:51265595 | TTTTGAGACAGTCTC[A/G]CTCTTTTGCCCAGGC | 51096 |
rs556756780 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51297136 | TTATTTAGAGGGGTG[A/G]GTTGGAAGTAGATCA | 51096 |
rs556765813 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51284848 | GGTGGATCACCTGAG[A/G]TCAAGAGTTCGAGAC | 51096 |
rs556809980 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | UTP18 | GRCh38.p7 | 17:51298124 | TCCCCCTTCCTGAAT[C/T]GATCCTCCATGCTTT | 51096 |
rs556918016 | snp | A/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51271842 | CTGGCTAATTTTTGT[A/T]TTTTTAGTAGACACG | 51096 |
rs556931141 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UTP18, MBTD1 | GRCh38.p7 | 17:51259785 | GGTCGGAGAGCTGCA[A/G]GCGTCCCCCCCACCT | 51096 |
rs556936885 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51291460 | TTAAAAATAGGTCAG[C/G]TGCAGTGGCCCACAC | 51096 |
rs557239623 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | UTP18, MBTD1 | GRCh38.p7 | 17:51260488 | GCGCAGGCTCCTTCC[A/G]GCCCCCGGGGCTTCG | 51096 |
rs557394654 | in-del | -/A | | | intron-variant | UTP18 | GRCh38.p7 | 17:51269123 | AAACCCCATCTCTAC[-/A]AAAAAATACAAAAAT | 51096 |
rs557398874 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51272894 | GGGAAAAGCAGCCCT[A/G]TTTGCTCTTTTTGAA | 51096 |
rs557446916 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51261406 | CGTGTATTCCGTTCA[C/T]TTAGCAAATATTGGT | 51096 |
rs557476539 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51281072 | AATCCCAGCTAGTTG[A/G]GAGGCTGAGGCAAAG | 51096 |
rs557531908 | snp | A/C | | | intron-variant | UTP18 | GRCh38.p7 | 17:51292277 | TAGAAGTGAAGTCCA[A/C]ATTGGGGTACTGCCA | 51096 |
rs557539865 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | UTP18 | GRCh38.p7 | 17:51274644 | TTTGGTAGAGACAGG[G/T]TTTCTCCATGTTAGT | 51096 |
rs557596779 | snp | G/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51267995 | GTACCAGTTGTTGTT[G/T]TTTTGTTTTTTGTTT | 51096 |
rs557814691 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51282580 | GATGAAATGGCCCTT[A/G]GCCCTGGTAGAGAGA | 51096 |
rs557824157 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51295926 | TAATATTTCCACTTT[C/T]TTCGTGCCTTATGTT | 51096 |
rs557880097 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51282710 | TGTATTTACAAATTT[A/G]GTCATGGCTGTGGAG | 51096 |
rs557925906 | snp | C/T | 0 | 0 | intron-variant | UTP18 | GRCh38.p7 | 17:51269095 | AGTTTAAGACCAGAC[C/T]GGGTGACATGGCGAA | 51096 |
rs557925943 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51262661 | CAAGTGATCCTCCTG[C/T]CTCTGCCTCCCAAGT | 51096 |
rs557946868 | snp | A/G | 0.000101464 | 0.00712193 | missense | UTP18 | GRCh38.p7 | 17:51293907 | ATCTCCTGCAGGTTC[A/G]TCTTCCTTCCTGTAC | 51096 |
rs557986791 | snp | A/G | 1.65658e-05 | 0.00287795 | missense | UTP18 | GRCh38.p7 | 17:51263317 | CAGAAGTGGAGAATG[A/G]AGCAAAAGGTAATTT | 51096 |
rs558077857 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51280714 | GCTACTTGAGAGGCT[G/T]AGGTGAGAGAATCTC | 51096 |
rs558131701 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51287822 | TAGCCTTCAAGAAGT[C/T]AACAGAAGGGGGAGA | 51096 |
rs558155544 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51296894 | CTTCCTAAGTGCCCT[G/T]CTGTGATCTAATTGA | 51096 |
rs558363467 | snp | A/T | 0.000798403 | 0.0199641 | downstream-variant-500B | UTP18 | GRCh38.p7 | 17:51298155 | AGGGGATCAGCTAAC[A/T]GGTAGTCTCTTGAGC | 51096 |
rs558479437 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51276236 | ACTGTTTTCAATCAC[A/C]GCTGCTCACCCCTTG | 51096 |
rs558532118 | snp | C/T | | | intron-variant, downstream-variant-500B | UTP18 | GRCh38.p7 | 17:51289474 | GGGCTCCCAAAGTGC[C/T]GGGATTACAGGAGTG | 51096 |
rs558541508 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51269934 | AATCTCAGCTCACTA[C/T]AACCTCTGCCTCCCG | 51096 |
rs558575207 | snp | G/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51271582 | AGTCTGGGTATATTT[G/T]TCTGATTCGTTTTCT | 51096 |
rs558583578 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51264931 | CAAGTGACCTGTTTG[C/T]CTCGGCCTCCTAAAG | 51096 |
rs558669088 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51292711 | CAATTGTGGCCTAAA[A/G]GTAACTGCTTCCATA | 51096 |
rs558685140 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51262880 | TCTTAAGGAGGTAGG[A/G]GGTCAAAAACAGATT | 51096 |
rs558699888 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51295677 | AGGATTGACTTGGCT[A/G]TGCGGGCTCTTTTTT | 51096 |
rs558705849 | snp | A/G | 0.00676609 | 0.0577691 | upstream-variant-2KB, intron-variant | UTP18, MBTD1 | GRCh38.p7 | 17:51259696 | GGAAGGGGGAGGGGG[A/G]CTCCGGAGGTTGAGA | 51096 |
rs558815469 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51272418 | CATAGTATTTTTAAG[A/G]TTTGTGTCTGATAAT | 51096 |
rs558883032 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UTP18 | GRCh38.p7 | 17:51284904 | TGTCTCTACTAAAAA[C/T]ACAAAAATTAACTAC | 51096 |
rs558925534 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51264346 | CTGCTGTGCCCAGCC[C/T]TATTTTTCCCTTTAA | 51096 |
rs558946485 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51278435 | CAAAAGTAATGGATT[C/T]TGGCATCTCCTTGTC | 51096 |
rs559004704 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51278122 | TTTAGCATTTCCAAT[C/T]TTTTCTTTCCTGTGT | 51096 |
rs559036928 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51277590 | TTAGCAGTTGATGCA[A/G]CAGAAAAAGCATGAG | 51096 |
rs559045480 | snp | A/G | 1.67419e-05 | 0.00289321 | synonymous-codon | UTP18 | GRCh38.p7 | 17:51266248 | TGAAAGTAAACTTTC[A/G]AAAGACAACCTTAAA | 51096 |
rs559125043 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51291626 | TGTAATCCCAGCTAC[C/T]CAGGAGGCTGAGACA | 51096 |
rs559201317 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51284397 | GCCTTTTTTTTTTAA[G/T]CATTTAAATAACTTG | 51096 |
rs559383727 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51272174 | CGCAATCTCAGCTCA[C/T]TGCAACCTCTGCCTC | 51096 |
rs559480101 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51284493 | CACTTCTTCCTCTTC[C/T]ATCATCATTAACATT | 51096 |
rs559516350 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51291980 | TTTTTTCCTGATCAT[C/T]TGCTTTCCTGATGCT | 51096 |
rs559543633 | snp | C/G | | | intron-variant, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51261661 | AGATAAACGAGTAAA[C/G]TTCAGGTTTGTTGGT | 51096 |
rs559655420 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51293448 | CCCACGGCGCAGGAC[G/T]GTTTGATTGTGGCCC | 51096 |
rs559709516 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51267025 | TAGGAATGGGGTTTC[A/G]CTATGTTGCTCAGGC | 51096 |
rs559838286 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | UTP18 | GRCh38.p7 | 17:51287191 | TATAGGAAAGAATCT[A/G]ATACTAGTAGCTTAA | 51096 |
rs560062275 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51261016 | GGAGCCTGGGCGACC[A/T]GCGGCGGCGGGGAGC | 51096 |
rs560178519 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51276336 | TTCAGTGTACAAGGA[A/T]CCATAATAATAGGGG | 51096 |
rs560284148 | snp | C/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51283386 | TTGGCCAGGCTGGTC[C/T]TGAACTACTGACCTC | 51096 |
rs560390008 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UTP18 | GRCh38.p7 | 17:51281411 | ATTAAAATAAAATTT[C/T]ACATGCCTTTTTTTC | 51096 |
rs560392486 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51280799 | GCCTGGGGGACAGAA[C/T]GAGACTCCATCTCAA | 51096 |
rs560394199 | snp | A/C | 0.000798403 | 0.0199641 | downstream-variant-500B | UTP18 | GRCh38.p7 | 17:51298220 | AAATCTCACGTAGTG[A/C]AGTTTGAACTTCCAA | 51096 |
rs560436227 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51295377 | GAATTAATTTTTGTA[G/T]AAGGTGTAAGGAAGG | 51096 |
rs560451563 | snp | A/G | 0 | 0 | intron-variant | UTP18 | GRCh38.p7 | 17:51282118 | AGCTACATAATCTTA[A/G]TATAGCTAATGCTGT | 51096 |
rs560452185 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51274142 | ACATGCTGCTAGGTC[C/T]TTTCTTGCCTGTGAA | 51096 |
rs560480682 | snp | A/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51275269 | CAAAACACATACTTT[A/T]GTTTTTAACTGAATT | 51096 |
rs560500822 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | UTP18 | GRCh38.p7 | 17:51298178 | TCTTGAGCTATGGAG[A/G]TCAGTCGGCTTGATA | 51096 |
rs560552925 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51281532 | TGAAATGATGAAATC[A/G]TAGAAATAGAGAATA | 51096 |
rs560663462 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51269976 | TTGTTTTGTCTCAGC[C/G]ACCTGAGTAGCTGGG | 51096 |
rs560686788 | snp | A/T | | | intron-variant, downstream-variant-500B | UTP18 | GRCh38.p7 | 17:51287099 | GCAGAAATGATCTTC[A/T]CTCAGATTTGTGAAG | 51096 |
rs560689687 | snp | C/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51263584 | TTGTCACACTTCTGT[C/T]TCAGTCTCCTCTTTG | 51096 |
rs560725507 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UTP18 | GRCh38.p7 | 17:51262557 | TGCTAATAGTAACTG[A/G]TTGCTCTTCTTGTTG | 51096 |
rs560839288 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51297618 | GCAGATAGATTTAAT[G/T]AGGACAAAGGATTTT | 51096 |
rs560862295 | in-del | -/AG | 0.00119737 | 0.0244387 | intron-variant | UTP18 | GRCh38.p7 | 17:51283357 | ATTTTTAATAGAGAC[-/AG]GGTTTCATCATGTTG | 51096 |
rs560862520 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51284212 | TTCACTGAATTCTCA[G/T]TGGGAGAATAAGAGT | 51096 |
rs561008124 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51276929 | AACCCAGAAGCTCTC[C/T]GAATACCTTCTGTTA | 51096 |
rs561124250 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | UTP18 | GRCh38.p7 | 17:51284322 | GTGAGGATCCACTTT[C/T]GAGATGGATGTAGGG | 51096 |
rs561125281 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51264409 | TCTTTATGTATAAAC[C/T]TTTCTTTATTTTCTA | 51096 |
rs561140443 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UTP18, MBTD1 | GRCh38.p7 | 17:51258807 | CTTTAGCTTCCTGTA[C/G]AAAAACATCTTCAGG | 51096 |
rs561179323 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UTP18, MBTD1 | GRCh38.p7 | 17:51259455 | GTGCTCCCCCTCCCC[A/G]CCAAGAAGAGAGGAC | 51096 |
rs561324870 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, utr-variant-5-prime, intron-variant, nc-transcript-variant | UTP18, MBTD1 | GRCh38.p7 | 17:51260046 | CCAGGATATCAACAA[C/T]ATTAGCATAGCCCTC | 51096 |
rs561471408 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | UTP18 | GRCh38.p7 | 17:51270711 | TTATTGGCCTTTCCT[G/T]GAAATGGTACAGGAT | 51096 |
rs561476036 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51267692 | CCAGACACTGCCCCT[C/T]AAAGTCCAGTTGTAT | 51096 |
rs561528350 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UTP18 | GRCh38.p7 | 17:51271474 | ACCATGCCCAGCTAA[C/T]GAAAAAAAAAATTTT | 51096 |
rs561561283 | in-del | -/CCAGTCATTCCCC | 0.000399441 | 0.0141266 | intron-variant | UTP18 | GRCh38.p7 | 17:51277330 | GTTGAATGCACACAA[-/CCAGTCATTCCCC]CCAGTCATTCCCCCC | 51096 |
rs561569656 | snp | C/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51274476 | AGACAGAGTTTTGCT[C/G]TTTTGCTCAGGCTGG | 51096 |
rs561690170 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51279162 | AAAAATCTACTATGT[A/G]GAAATGAATGGATAG | 51096 |
rs561700111 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51294601 | ATCCAGTCTATCATT[G/T]TTGGACATTTGAGTT | 51096 |
rs561811597 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51285563 | ATATTACAGTAGTTC[C/T]CCCCTTATCTGCAGT | 51096 |
rs561849130 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51261105 | CGCCTCCCTGCTCCA[A/G]ACTGAAAGTGCCTGG | 51096 |
rs561874519 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51292650 | GAACATGAAGGTGCT[A/G]TATCTCTTGGGAGAG | 51096 |
rs561885436 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51272406 | GCCTGGCCTGAACAT[A/G/T]GTATTTTTAAGGTTT | 51096 |
rs561955089 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51287363 | AGGGAGATGAGCCTT[A/G]AGGTCACTGCAGCAA | 51096 |
rs562020241 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | UTP18 | GRCh38.p7 | 17:51280823 | ATCTCAATAAAAAAA[A/T]TTTTTTTTTAGCCAT | 51096 |
rs562250945 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UTP18 | GRCh38.p7 | 17:51281185 | TTTAAACGAAAAGTT[A/G]TGTTTGGTTTTAAAG | 51096 |
rs562497324 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51263589 | ACACTTCTGTCTCAG[C/T]CTCCTCTTTGCTGTA | 51096 |
rs562548460 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51270071 | GTGTTGGCCAGGCTG[G/T]TCTTGAACTCTTGGC | 51096 |
rs562569301 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51296098 | TGTCCAGGTTCTTTT[C/T]TGTACCCAACATACT | 51096 |
rs562670700 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51263008 | TTTGTTCTTGTCTTA[C/T]TTGGTGTTTTCCTTC | 51096 |
rs562672346 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UTP18 | GRCh38.p7 | 17:51265047 | TTAAATAATCTTGGT[A/G]TATTAGTTCCTGACA | 51096 |
rs562679184 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UTP18 | GRCh38.p7 | 17:51268317 | AGGCGTGAGCCATGG[C/T]GCCCGGCCCAGGTAC | 51096 |
rs562715071 | in-del | -/TTTTGTCT | 0.00119737 | 0.0244387 | intron-variant | UTP18 | GRCh38.p7 | 17:51283595 | TTCTAACTTTACTGG[-/TTTTGTCT]TTGTTTACTCATGGA | 51096 |
rs562740753 | snp | C/T | 0.000513884 | 0.0160212 | intron-variant | UTP18 | GRCh38.p7 | 17:51268793 | CAAGCTTTATGGACA[C/T]GTAGTGGTTGCCATA | 51096 |
rs562852308 | snp | C/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51291422 | CTTTTCCCGATATTC[C/G]AAGTCAGTAGCAGAG | 51096 |
rs563098801 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UTP18 | GRCh38.p7 | 17:51290170 | CCTGTAATCCCGGCA[C/G]TTTGGGAGGCTGAGG | 51096 |
rs563178535 | snp | G/T | 0.000399281 | 0.0141238 | downstream-variant-500B | UTP18 | GRCh38.p7 | 17:51298272 | TGGAAATGAAAAGGC[G/T]TTTCTGGCCTTATTA | 51096 |
rs563241696 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51291159 | AGCACTTTGTGAGGC[C/T]GAGGCAGATGGATCA | 51096 |
rs563244984 | in-del | -/TGTT | 0.0023933 | 0.0345097 | intron-variant | UTP18 | GRCh38.p7 | 17:51297556 | TTCATCACAGTTGAC[-/TGTT]TGGTCTCCTCAGAGA | 51096 |
rs563284903 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UTP18 | GRCh38.p7 | 17:51278350 | GGTTAAAAAGTCTTA[A/C]ACCATCTTCTCATAT | 51096 |
rs563380022 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UTP18 | GRCh38.p7 | 17:51277720 | ATAATAAAATTTTGA[C/T]TTATATTTAAAGGGA | 51096 |
rs563415398 | snp | C/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51296631 | GGCCATTAGATTTTC[C/T]ACCAGAGCATTGCTC | 51096 |
rs563420334 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51271610 | TCTAGACCACAAATT[A/C]TCTCTACAGCTAATT | 51096 |
rs563490592 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | UTP18, MBTD1 | GRCh38.p7 | 17:51259532 | ATCCAGCCTTTCCCC[C/T]CTAGCCAGAGCAGGG | 51096 |
rs563770517 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51293441 | TGTCCAACCCACGGC[C/G]CAGGACGGTTTGATT | 51096 |
rs563807283 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51268257 | GGTCTCAATCTCCTG[A/G]CCTCGTGATCCGCCC | 51096 |
rs563880108 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51265934 | ATTTCATAAACTGTG[C/T]GCAGATAAGTCATGA | 51096 |
rs564040886 | snp | A/C | 1.82877e-05 | 0.00302383 | missense, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51260605 | GCCGGAGCGGAGGAG[A/C]CGAATGAAACTGGAC | 51096 |
rs564110647 | snp | A/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51277831 | ATTTATCTGCCCTCT[A/T]CCATACCCATTCTTT | 51096 |
rs564235468 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51285848 | GGGTCTTGGAACATA[C/T]GCCCTGCCAGATAAG | 51096 |
rs564435571 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | UTP18 | GRCh38.p7 | 17:51287481 | TGCTTAGAAGATGGG[G/T]AGTGGGAGAGAAGTA | 51096 |
rs564556725 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51294729 | ACCCAGTAATGGGAT[G/T]GCTGGGTCAAATGGT | 51096 |
rs564828996 | snp | G/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51288480 | CTTTTAGTATTAATG[G/T]TAAGGACTATATTTA | 51096 |
rs564893516 | snp | C/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51290683 | AGACACATAATAGTT[C/T]TGCATTGTTTGCTTC | 51096 |
rs564907707 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | UTP18 | GRCh38.p7 | 17:51289481 | CAAAGTGCTGGGATT[A/G]CAGGAGTGAGCCGCC | 51096 |
rs564946788 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51265248 | ATATTTTTACTTCAT[A/C]GTATTTTAAGGTTTG | 51096 |
rs564969648 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51290389 | CCTCTGTACTCCAGC[C/T]TGGGTGACAGAGTAA | 51096 |
rs564975470 | snp | A/C | | | intron-variant | UTP18 | GRCh38.p7 | 17:51266680 | GAGAGTAAGGTACAG[A/C]TAATGCGACACTTAA | 51096 |
rs565006109 | snp | G/T | | | intron-variant, downstream-variant-500B | UTP18 | GRCh38.p7 | 17:51289255 | AGGCTGGACTGCAGT[G/T]GTGTGATCTCGGCTC | 51096 |
rs565012030 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UTP18, MBTD1 | GRCh38.p7 | 17:51259585 | AAACTTTCTTCTCGA[A/T]TTTTTCTTCCAAAGG | 51096 |
rs565012150 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51265655 | TTCAACCTCTGCCTC[C/T]TGGGTTCAAGTGGTT | 51096 |
rs565096196 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UTP18 | GRCh38.p7 | 17:51269354 | GTTTTTTGACTGTAG[A/G]TTTTAAATTTAACTT | 51096 |
rs565147484 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51271407 | GACCTCCTGGGTTCA[A/G]GCAATCCTCCCACCT | 51096 |
rs565155534 | in-del | -/A | | | intron-variant | UTP18 | GRCh38.p7 | 17:51263932 | CATTTCTCCCTACTT[-/A]AAAAAAAATAGACAT | 51096 |
rs565226955 | snp | A/G | 0.000798403 | 0.0199641 | downstream-variant-500B | UTP18 | GRCh38.p7 | 17:51298326 | TTGAAGAGGAGCCAT[A/G]GTAAACCTGGTAGCC | 51096 |
rs565421075 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UTP18, MBTD1 | GRCh38.p7 | 17:51258762 | TGCACTCCTAAGAGA[A/C]AACAGGCACGAAATT | 51096 |
rs565499645 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51283510 | TGTGTGATTAGTAAC[A/C]TATTGTTCACATTAC | 51096 |
rs565553305 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51284109 | TATTTGATCCTATTC[A/G]GTTTTCCCAAATGTG | 51096 |
rs565608939 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UTP18 | GRCh38.p7 | 17:51269022 | CCTGGCTCGGTAGCT[C/T]ACGCCTGTCATCCCA | 51096 |
rs565614791 | snp | A/G | | | intron-variant, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51261184 | GTATCTGCTTTGCGA[A/G]CTGTGGTCGTGAGCA | 51096 |
rs565615208 | snp | C/T | 1.65619e-05 | 0.00287762 | missense | UTP18 | GRCh38.p7 | 17:51277230 | AAGAAGTTTTAGCCA[C/T]GAGTACCCACAGCAA | 51096 |
rs565642478 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51267108 | GCTGGGACTGCAGGT[C/G]TGTGCCACCATGCCC | 51096 |
rs565668480 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UTP18 | GRCh38.p7 | 17:51292337 | TTCTCATTAGCACCA[C/T]TGCCTTCACATTGAT | 51096 |
rs565670998 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51265421 | GGCTCCTGCCACCAC[A/G]CTGGACTAATTTTGT | 51096 |
rs565805727 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, utr-variant-5-prime | UTP18, MBTD1 | GRCh38.p7 | 17:51260224 | TTGTGTCAAGTCAAG[C/T]GGTTACAGCCAAGAG | 51096 |
rs565897006 | snp | G/T | | | upstream-variant-2KB, utr-variant-5-prime, intron-variant | UTP18, MBTD1 | GRCh38.p7 | 17:51259175 | GCAGAGGGGACGGCT[G/T]CTTTGGATGACCTCT | 51096 |
rs565957685 | in-del | -/T | 0.00174261 | 0.0294664 | intron-variant | UTP18 | GRCh38.p7 | 17:51285212 | AAGTTTAAAGCAAAA[-/T]TTAACAACTCTTTTT | 51096 |
rs566046358 | snp | C/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51264354 | CCCAGCCTTATTTTT[C/G]CCTTTAATGCAGATT | 51096 |
rs566079505 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UTP18 | GRCh38.p7 | 17:51272744 | TAGCCCTTTGTGGCC[A/G]CAATCCAAAATCTGG | 51096 |
rs566097403 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51285916 | CAAAGAAAATGCTGG[C/T]GCTACCTTATATCAT | 51096 |
rs566167533 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51281214 | AGTTTCTTTTTAGCT[A/G]GAAAATCAGATCTAT | 51096 |
rs566205284 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51266687 | AGGTACAGATAATGC[A/G/T]ACACTTAACTCATTA | 51096 |
rs566236357 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UTP18 | GRCh38.p7 | 17:51292915 | TCATGATTCAGCCCT[C/T]TTCGAGGAGAAATTG | 51096 |
rs566289031 | snp | A/G | 6.00667e-05 | 0.00547994 | synonymous-codon, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51260662 | GAAGCCCGGAATGAG[A/G]CCGGACTGGAAAGCC | 51096 |
rs566392597 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51261347 | ATCTCCGTTGTAACT[A/G]TGTCCCCATGTGACT | 51096 |
rs566426451 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51293683 | GCAAGAAATTCATGT[A/G]GCAAAACTGCAGCTG | 51096 |
rs566551593 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UTP18 | GRCh38.p7 | 17:51294791 | ACACTGACTTCCACA[A/G]TGGTTGAACTAGTTT | 51096 |
rs566679205 | snp | C/T | 1.88738e-05 | 0.0030719 | intron-variant | UTP18 | GRCh38.p7 | 17:51280528 | TTTTACATTTTAAAT[C/T]TTAGGCCAGGCGCGG | 51096 |
rs566735462 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UTP18 | GRCh38.p7 | 17:51280948 | TTTGGGAGGCTGAGG[C/T]GAGTGGATCGTTTGA | 51096 |
rs566862572 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UTP18 | GRCh38.p7 | 17:51275145 | GAGGTTGTGGTGAGT[C/T]GAGATTACGCCATTG | 51096 |
rs566939798 | snp | G/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | UTP18, MBTD1 | GRCh38.p7 | 17:51259593 | TTCTCGAATTTTTCT[G/T]CCAAAGGGTGGAGGA | 51096 |
rs567001774 | snp | C/T | | | intron-variant, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51261829 | CCTAGTTAATGTCAG[C/T]TGCTTACCAGAGCCG | 51096 |
rs567005164 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UTP18 | GRCh38.p7 | 17:51287633 | TTAGGAATGCAGTGC[A/G]TAATTAGGACTAAAG | 51096 |
rs567027757 | in-del | -/AA | 0.00199481 | 0.0315187 | intron-variant | UTP18 | GRCh38.p7 | 17:51275179 | TCCAGCCTGGGCAAC[-/AA]GAGTGAAACCCAGTC | 51096 |
rs567204848 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UTP18 | GRCh38.p7 | 17:51282577 | CCTGATGAAATGGCC[C/T]TTGGCCCTGGTAGAG | 51096 |
rs567227974 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51269796 | TATCCACTGCAGTAA[C/T]CTTTTCTACATTATC | 51096 |
rs567350915 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51276571 | TCTAACACTGATGTA[C/G]ATTGATGGTTTCTTG | 51096 |
rs567412185 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51270267 | AAACATATAGATTAT[C/G]TTCTTTTTCTCTCAT | 51096 |
rs567540415 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | UTP18 | GRCh38.p7 | 17:51289619 | CCTAATCTTCAGGCA[A/G]AGCCAATTTTCTCAT | 51096 |
rs567628824 | snp | A/C | 0.000399281 | 0.0141238 | downstream-variant-500B | UTP18 | GRCh38.p7 | 17:51298368 | ATTATTAGCCACTGC[A/C]CTTCCTGGAAATGTT | 51096 |
rs567654764 | in-del | -/TTT | 0.00199481 | 0.0315187 | intron-variant | UTP18 | GRCh38.p7 | 17:51284385 | AGCTTGTGTTTAGCC[-/TTT]TTTTTTTAATCATTT | 51096 |
rs567677731 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51291380 | AGATGCTGTTGATCT[A/C]TTAGGACATTGTAAA | 51096 |
rs567739736 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51283859 | GCCTCAAGTGAGCCA[A/C]CTGCCTTGGCCTCCC | 51096 |
rs567749839 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UTP18 | GRCh38.p7 | 17:51292852 | CTGGCTTTGAGGTGA[A/G]CTTTTGGCTCTCTCT | 51096 |
rs567814827 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51273538 | GATGTATGGATTCCT[A/G]TTATCTGTGGGGTTA | 51096 |
rs567828567 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51265358 | AGCTTCTGCTTCCCA[A/G]GTTCAAGTGATTCAC | 51096 |
rs567892999 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UTP18, MBTD1 | GRCh38.p7 | 17:51259613 | AGGGTGGAGGAGATG[A/G]AGAGAACCCCAACGA | 51096 |
rs567931359 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UTP18 | GRCh38.p7 | 17:51277942 | GAGGTTGTCTGGCTA[A/G]TCTCAGGAGGTAGTG | 51096 |
rs567971377 | snp | C/T | 0.000798403 | 0.0199641 | downstream-variant-500B | UTP18 | GRCh38.p7 | 17:51298023 | AGAAATTGGAAACAC[C/T]TGTCTGTAGCCAAAA | 51096 |
rs568030637 | snp | C/T | 0.000569019 | 0.0168578 | missense, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51260760 | CGAGCGCGGCGGCCG[C/T]TGCGATTGCAGTCGC | 51096 |
rs568128902 | snp | C/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51269031 | GTAGCTCACGCCTGT[C/T]ATCCCAGTGCTTTGG | 51096 |
rs568351077 | snp | G/T | 0.00874735 | 0.0655527 | intron-variant | UTP18 | GRCh38.p7 | 17:51293505 | ACATGAGTTGTTGTT[G/T]TTTTTTTTTTTAAGC | 51096 |
rs568546105 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UTP18 | GRCh38.p7 | 17:51273621 | TTTTTCCTTTTGCAA[A/G]AAATGTTCTAGAGGT | 51096 |
rs568724707 | snp | C/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51291877 | GGTGAGTGAATGCCT[C/G]AGGCCTAGTTTCATA | 51096 |
rs568796140 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51287706 | TAAATGAGATGAATG[A/G]GACACTAGAAGTAGG | 51096 |
rs568855201 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51281058 | TGGCGCTCGCCTGTA[A/G]TCCCAGCTAGTTGGG | 51096 |
rs568869233 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UTP18 | GRCh38.p7 | 17:51271699 | TTTTGAGTTAGTCTT[C/G]CTCTGTCGTGTAGGC | 51096 |
rs568918516 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51263997 | TTAACCATAATTTAC[A/G]TGGCTATTGTTGGGT | 51096 |
rs568943783 | snp | A/C | | | intron-variant | UTP18 | GRCh38.p7 | 17:51278572 | GCTTTGGAGACATGG[A/C]ATTGATCTTTCCTTC | 51096 |
rs568962791 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51261767 | AAAGGGGGCAGAGGA[A/T]AGCTCACCGAGAATT | 51096 |
rs568971337 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51288383 | GCACAGTAGCCACCA[C/T]ATTTGATTATGTCAC | 51096 |
rs569101175 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51262358 | CAAAGTGCTGAGACT[A/G]CAAGTGTGAGCCACC | 51096 |
rs569128987 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UTP18 | GRCh38.p7 | 17:51275295 | GAATTTTAAAAATTC[A/G]AGGGGAAACCTGTAA | 51096 |
rs569251468 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | UTP18 | GRCh38.p7 | 17:51272585 | TCTAGGATGATGGTT[C/T]ATATGTTTACTTCTA | 51096 |
rs569467712 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51294446 | TGAGTGAGAACATGC[A/G]GTGTTTGGTTTTTTG | 51096 |
rs569483032 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | UTP18 | GRCh38.p7 | 17:51289625 | CTTCAGGCAGAGCCA[A/G]TTTTCTCATTCATTT | 51096 |
rs569486933 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51297746 | ATGACCAGCAGCTAT[A/C]AATCAGGTATGTAAT | 51096 |
rs569494747 | snp | A/C/G | 0.000132527 | 0.00813937 | synonymous-codon | UTP18 | GRCh38.p7 | 17:51263294 | AGAACATGAAGACTC[A/C/G]GGTGACTCAGAAGTG | 51096 |
rs569551393 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51290605 | CCTTTTATCACTTTA[A/G]TGGTAGTAAATTGTT | 51096 |
rs569552594 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UTP18 | GRCh38.p7 | 17:51292826 | GTGTGTGTTCCTCCT[C/T]ATACTTACGTCTGGC | 51096 |
rs569590772 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51276662 | GTATAGATGGTGAAC[A/G]CATGGTCACAAATGT | 51096 |
rs569705118 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51291415 | TCCCCTCCTTTTCCC[A/G]ATATTCCAAGTCAGT | 51096 |
rs569751948 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51264871 | TATTTTTAGTAGAGA[C/T]GGGGTTTTACCATGT | 51096 |
rs569771364 | snp | C/G | 0.00914312 | 0.0669923 | intron-variant | UTP18 | GRCh38.p7 | 17:51270665 | AGATGTTGACATCCA[C/G]TTGGCTTATAGGAGG | 51096 |
rs569787787 | in-del | -/T | 0.0023933 | 0.0345097 | intron-variant | UTP18 | GRCh38.p7 | 17:51265054 | ATCTTGGTATATTAG[-/T]TCCTGACATATTGAG | 51096 |
rs569862271 | snp | C/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51268272 | ACCTCGTGATCCGCC[C/T]GCCTTGGCCTCCCAA | 51096 |
rs569932172 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51283142 | CCAAAGTGCTAGGAT[C/T]ACAGGCGTGAGCCAC | 51096 |
rs570036097 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51292216 | ATATATATACTTAAA[A/C]GTAATTTCTCGAGGA | 51096 |
rs570121702 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51261270 | GATCACCTGCCTCAG[A/T]TCCTTGTGATTCAGG | 51096 |
rs570128691 | snp | C/T | | | intron-variant, utr-variant-3-prime | UTP18 | GRCh38.p7 | 17:51288919 | ACAACATGTGTTAAG[C/T]GTTTTCTACCTGGGA | 51096 |
rs570224196 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | UTP18, MBTD1 | GRCh38.p7 | 17:51260157 | GGGACCCTCTGCAGG[A/C]TCCGTACTCCAAGGA | 51096 |
rs570372583 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51291522 | AGAGGATCACTTGAG[G/T]CCAGGAGTTTGAGAC | 51096 |
rs570398187 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UTP18 | GRCh38.p7 | 17:51266619 | TAACATTTTGTCATA[C/T]TTGCTTTGTGTATTT | 51096 |
rs570514786 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UTP18 | GRCh38.p7 | 17:51278805 | TTGGATTAAAATTAC[C/T]CTTAATAGGCATAGT | 51096 |
rs570540830 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51296383 | GGTTTTGAGGAAATA[A/G]TTGTGAAAGGAGAAT | 51096 |
rs570547472 | snp | A/C | | | intron-variant | UTP18 | GRCh38.p7 | 17:51291748 | GATCTCAAAAAAAAA[A/C]AAAAAGAAAAGAAAA | 51096 |
rs570683277 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51286127 | ATACCATTTGATAGT[A/G]TTGTAGAAACTTTAA | 51096 |
rs570744552 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | UTP18 | GRCh38.p7 | 17:51286815 | CTGTTTAAACTCATT[A/G]TAAGTAGTTTTTAAA | 51096 |
rs570883521 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51268102 | GCAAGCTCTGCCTCC[C/T]GGGTTCACACCATTC | 51096 |
rs570942889 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UTP18 | GRCh38.p7 | 17:51268323 | GAGCCATGGCGCCCG[G/T]CCCAGGTACCAGTTC | 51096 |
rs570944743 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51261890 | AATCTTTTTGGGAAG[C/T]ACAGAACTATTACTG | 51096 |
rs571005628 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51262417 | TATAAACTTTATGGT[A/G]TAAATTTATAACTTT | 51096 |
rs571115554 | snp | A/G | 0.002557 | 0.0356645 | intron-variant | UTP18 | GRCh38.p7 | 17:51267402 | AATTTGGTGGCATTT[A/G]GTATATTTAGAATGT | 51096 |
rs571174831 | snp | C/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51264376 | ATGCAGATTATTTCA[C/G]CATTAATGTTTATCA | 51096 |
rs571319380 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | UTP18, MBTD1 | GRCh38.p7 | 17:51259076 | GAACTACTGAAATAT[A/G]GGCTTTCCTGGGCAG | 51096 |
rs571362811 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51282412 | CATATAAGGCCAGGA[A/G]CAGCTATATTTTCTA | 51096 |
rs571385798 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | UTP18 | GRCh38.p7 | 17:51283069 | AGACGGGGTTTTCTT[G/T]TGTTGCCCAGGCTGG | 51096 |
rs571510941 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51295612 | CTGTAGCCTTGTAGT[A/G]TAGTTTGAAGTCAGG | 51096 |
rs571556965 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51287875 | GTTTGGTTGGAGGTT[C/T]TATAGGACATCTGTG | 51096 |
rs571710038 | snp | A/G | | | upstream-variant-2KB, intron-variant | UTP18, MBTD1 | GRCh38.p7 | 17:51258992 | AATTTGAGAAGTAAA[A/G]AAAGGAGCAACTTAA | 51096 |
rs571835869 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | UTP18 | GRCh38.p7 | 17:51269718 | TAAGTAGAAATTGAC[C/T]GTCTTTGTTTCTAGC | 51096 |
rs572047912 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | UTP18 | GRCh38.p7 | 17:51298159 | GATCAGCTAACAGGT[A/G]GTCTCTTGAGCTATG | 51096 |
rs572119124 | in-del | -/TATT | 0.000743205 | 0.0192627 | intron-variant | UTP18 | GRCh38.p7 | 17:51280374 | CAGTTTGATAAATAA[-/TATT]TATTGTTTTAGACCA | 51096 |
rs572219077 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51269948 | ACAACCTCTGCCTCC[C/T]GGGTTCCAGTGATTG | 51096 |
rs572222680 | snp | A/C/G | | | upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51260517 | CGGCGGCGGCGGCCC[A/C/G]CGAGGGGCCTGGGCG | 51096 |
rs572224141 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51270414 | AAACATAATTTTATT[A/G]TCCATTTCAGAATGC | 51096 |
rs572245450 | snp | C/T | 2.43792e-05 | 0.00349128 | utr-variant-5-prime, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51260547 | GCATGCGCAGCGAGG[C/T]TCCACGTGAGCGCCT | 51096 |
rs572360000 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51271414 | TGGGTTCAAGCAATC[C/T]TCCCACCTCAGCCTC | 51096 |
rs572362535 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51271998 | TTTAATTACGTATTT[G/T]TCAGCTCTAGAATTT | 51096 |
rs572407074 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UTP18 | GRCh38.p7 | 17:51264934 | GTGACCTGTTTGCCT[C/T]GGCCTCCTAAAGTGC | 51096 |
rs572420353 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UTP18 | GRCh38.p7 | 17:51265717 | TACAGGTGTGTGCCA[C/T]CCCGCCCAGCTAATT | 51096 |
rs572421446 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UTP18 | GRCh38.p7 | 17:51278131 | TCCAATCTTTTCTTT[C/T]CTGTGTTCCTGACAC | 51096 |
rs572425345 | snp | A/G/T | 5.29323e-05 | 0.0051443 | intron-variant | UTP18 | GRCh38.p7 | 17:51266287 | TAAAGAAGAGTAAGT[A/G/T]TCTTTTTTCATATGA | 51096 |
rs572456562 | snp | C/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51276913 | CCTCCGTGTGTTCAG[C/T]AACCCAGAAGCTCTC | 51096 |
rs572500386 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51281538 | GATGAAATCGTAGAA[A/G]TAGAGAATAGATTAG | 51096 |
rs572511630 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51291652 | AGACAGAAGAATTGC[C/T]TGCCCCCAAGAGGCG | 51096 |
rs572535398 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51279141 | GCAATATATTCACAC[A/G]GTGTTAAAAATCTAC | 51096 |
rs572563456 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51283534 | ACATTACATTGTTAC[A/G]TGTAAAGAATAATTT | 51096 |
rs572597183 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51279615 | TGTTTTTGGCTGTCT[C/T]TAGTGGCAGTGTATT | 51096 |
rs572640831 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UTP18 | GRCh38.p7 | 17:51283513 | GTGATTAGTAACATA[G/T]TGTTCACATTACATT | 51096 |
rs572704146 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51284151 | CTTAACCTGCACGCT[A/T]ACTCTAGCCTGGAAC | 51096 |
rs572714637 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51285476 | CTCTTTATAAACTAT[C/T]CAGTAATATGAAATT | 51096 |
rs572762535 | snp | C/G/T | 0.00199529 | 0.0315338 | intron-variant | UTP18 | GRCh38.p7 | 17:51275357 | ATGGATGTGAGATTA[C/G/T]CATTACTTTAAACTT | 51096 |
rs572770449 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51277619 | AGCCATGGAGCTAGA[A/C]GACCTGGATTCCATT | 51096 |
rs572992746 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51284761 | TGTATATGTGAATGT[A/G]TACAAGAAATATTCT | 51096 |
rs573204905 | snp | A/G | 0.0577344 | 0.159793 | intron-variant | UTP18 | GRCh38.p7 | 17:51294570 | TTCCATGGTGTATAT[A/G]TGCCACATTTTCTTA | 51096 |
rs573266427 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | UTP18 | GRCh38.p7 | 17:51287274 | CCAACAACCATTTAA[A/G]CTTTTAGAATCTTCA | 51096 |
rs573289287 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51295079 | AATTTGTTTGAGTTC[A/G]TTGTAGATTGTGGAT | 51096 |
rs573448394 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51269766 | TGAAGGAATCTTAGT[A/G]ATGTGGCCTGACTTT | 51096 |
rs573461269 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UTP18 | GRCh38.p7 | 17:51268150 | GAGTAGCTGGGACTA[C/T]CAGTAGATGGGACTA | 51096 |
rs573600397 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51269171 | ATGTTCCTGTAGTCC[C/T]GACTACTTGGGGGGC | 51096 |
rs573633694 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51275465 | CATTTGTGCCATGAA[C/T]GCAAAGATGCCAGGT | 51096 |
rs573660041 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51263524 | ATAGAAAAGATCTTT[C/G]ATGGTTCCTGATCCC | 51096 |
rs573695772 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UTP18 | GRCh38.p7 | 17:51264130 | CAACCTCTGCCTCCT[A/G]GGTTCAAGCGATTCT | 51096 |
rs573746055 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51287923 | TGGTCTCTTTGTAAC[A/G]TGATTCCTGTAAATA | 51096 |
rs573793449 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51276866 | GAGCGTGGAGCTTCC[A/G]TGCCTTCTCAGGGCA | 51096 |
rs573851585 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | UTP18 | GRCh38.p7 | 17:51280806 | GGACAGAACGAGACT[A/C]CATCTCAATAAAAAA | 51096 |
rs573924507 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UTP18 | GRCh38.p7 | 17:51290866 | AAAAACATTGTTAGC[A/G]TTGTTAAATGCAGTC | 51096 |
rs573975132 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51274847 | TGATTTTGTCTTGCA[C/T]CTTATGAGGACAATT | 51096 |
rs573984985 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51283414 | CTCAGGTGATCTGCC[C/T]GCCTTGGCCTCCCAA | 51096 |
rs574120890 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51265988 | TCCAAAGTGTAAACC[A/G]GATGATCTGAAATGT | 51096 |
rs574207379 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | UTP18 | GRCh38.p7 | 17:51292402 | AAGTTGAAAATAATT[C/G]AATGTGGCTTGGAGA | 51096 |
rs574251013 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51270486 | TTGGGTATGGTTATG[C/G]TAGCTGTTGAAACAA | 51096 |
rs574284481 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51289922 | TAATAAAGGGCAGAA[C/T]TGTGATTTAGATTCC | 51096 |
rs574320449 | snp | C/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51296078 | TAACCAAAACTTATA[C/T]GCGCTGTCCAGGTTC | 51096 |
rs574513702 | in-del | -/T | 0.00279162 | 0.0372561 | intron-variant | UTP18 | GRCh38.p7 | 17:51270158 | CTTTTTACTAAACTG[-/T]TTTTTCCCCTTCTTC | 51096 |
rs574576962 | snp | C/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51271657 | AACATCTATTGGAGG[C/G]TTAATTTAATTTTAT | 51096 |
rs574657722 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UTP18, MBTD1 | GRCh38.p7 | 17:51259500 | ACCCTGGGTGGCTAA[A/C]AAAGGAAAAGTCTCG | 51096 |
rs574719466 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51290033 | GTAGGGCAAGGAGGA[A/G]GCTAAGCTCCTTAAC | 51096 |
rs574732876 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51266326 | GAGGTGTATGTAACC[A/T]ATGCCCAGTCATTAA | 51096 |
rs574821112 | snp | G/T | 0.000955083 | 0.0218318 | missense, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51260926 | TCTGCGAGGCCCGAG[G/T]GTGAGGGAGGCCGCG | 51096 |
rs575072382 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51279019 | TTGTATTTTCCTGTA[A/G]TGGAACAAGGGTCCT | 51096 |
rs575101146 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51279869 | GCGTTTAGACTTATT[C/T]GGGGTCTGAGCCAGG | 51096 |
rs575204480 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51272115 | GTTGTTTGTGTTTTT[C/T]TGAGACAGAGTCTTA | 51096 |
rs575226665 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51280552 | GGCGCGGTGGCTCAC[A/G]TGTGTAATCCCACCA | 51096 |
rs575228722 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51274127 | TTTTCTGTTTCTTGG[A/G]CATGCTGCTAGGTCC | 51096 |
rs575279122 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UTP18 | GRCh38.p7 | 17:51295859 | GGGGAATATATATAT[A/T]TTTTGGAAAGCACTA | 51096 |
rs575392454 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51268242 | CATGTTAGCCAGGAT[A/G]GTCTCAATCTCCTGA | 51096 |
rs575455299 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51268531 | CTTTACATAGTCCTG[A/G]TATCTGGGATGTGTT | 51096 |
rs575456395 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51286356 | GGTTTTTGTGATTTT[C/T]TTAGACCAAACACAA | 51096 |
rs575555058 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51293843 | TAGAGTGAAGATTAC[A/G]ATTTAAGAAACATGA | 51096 |
rs575660042 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51281218 | TCTTTTTAGCTAGAA[A/G]ATCAGATCTATTTTT | 51096 |
rs575878007 | snp | A/C/G/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51262605 | CCTGCACAATTCTCC[A/C/G/T]AACACTTTAAACTCA | 51096 |
rs576066744 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51263600 | TCAGTCTCCTCTTTG[C/T]TGTATACAGTAGCTA | 51096 |
rs576068598 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51269895 | AATCTCACTCTGTCA[C/T]CCAGGGCTGGAGTGC | 51096 |
rs576078367 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UTP18, MBTD1 | GRCh38.p7 | 17:51258613 | GCGGTAATCATCTAA[C/T]CATCCCTCTACCAGG | 51096 |
rs576096725 | in-del | -/AAC | | | intron-variant | UTP18 | GRCh38.p7 | 17:51290418 | AGAGTCTGTCTCAAA[-/AAC]AACAACAACAACAAC | 51096 |
rs576102052 | snp | G/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | UTP18, MBTD1 | GRCh38.p7 | 17:51259389 | TGCAAACCGCCTCGC[G/T]GCACTGCCCCCAAGG | 51096 |
rs576127966 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51264248 | GACGGAGTTTTGCTA[C/T]GTTGGCCAGGCTGGT | 51096 |
rs576159820 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51281844 | AAAAAGATAAGGCAG[A/T]CATTATTTAAAAAAA | 51096 |
rs576222041 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51275513 | AAGTGAAATTTCCTC[A/T]GAAGTGAAAGTCTCT | 51096 |
rs576256774 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51276111 | TAAAACATCATAGCC[C/T]GAAGCATAGCTAAGT | 51096 |
rs576355418 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | UTP18 | GRCh38.p7 | 17:51283760 | GCTGGGATTACAGGC[A/C]TGTGCCACCACGCCC | 51096 |
rs576401566 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51269260 | GATAAGTGCCACCGT[A/G]CTCCAGCCTGGGTGA | 51096 |
rs576459006 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51284858 | CTGAGGTCAAGAGTT[C/T]GAGACCAGCCTGGCC | 51096 |
rs576534918 | snp | C/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51265720 | AGGTGTGTGCCACCC[C/T]GCCCAGCTAATTTCT | 51096 |
rs576538793 | snp | A/G | 8.30406e-05 | 0.00644309 | intron-variant | UTP18 | GRCh38.p7 | 17:51285411 | TAATCACATTGTGCT[A/G]ATGAGAATATGTTGA | 51096 |
rs576589417 | snp | G/T | 0.0123036 | 0.0774623 | intron-variant | UTP18 | GRCh38.p7 | 17:51265600 | AGACAGTCTCACTCT[G/T]TTGCCCAGGCTGGAG | 51096 |
rs576648866 | snp | C/T | 8.35722e-05 | 0.00646368 | missense | UTP18 | GRCh38.p7 | 17:51266201 | GACATGATGAACAAT[C/T]GGTTTCGGAAGGATA | 51096 |
rs576682849 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UTP18 | GRCh38.p7 | 17:51283491 | TATTCTGTATGGAGT[C/T]GTTTGTGTGATTAGT | 51096 |
rs576692541 | snp | C/G | 0.000399281 | 0.0141238 | downstream-variant-500B | UTP18 | GRCh38.p7 | 17:51298144 | CTCCATGCTTTAGGG[C/G]ATCAGCTAACAGGTA | 51096 |
rs576711888 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | UTP18, MBTD1 | GRCh38.p7 | 17:51260502 | CGGCCCCCGGGGCTT[A/C]GGCGGCGGCGGCCCG | 51096 |
rs576882875 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UTP18 | GRCh38.p7 | 17:51268233 | GGGTTTCACCATGTT[A/G]GCCAGGATGGTCTCA | 51096 |
rs576960577 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51292990 | AAATGGCAATTTTAT[C/G]ATAGTAGAATATATG | 51096 |
rs576991873 | snp | C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | UTP18, MBTD1 | GRCh38.p7 | 17:51259796 | TGCAGGCGTCCCCCC[C/G]ACCTGGCACACAAAG | 51096 |
rs577144056 | snp | C/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51263011 | GTTCTTGTCTTACTT[C/G]GTGTTTTCCTTCCTG | 51096 |
rs577203975 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51265371 | CAGGTTCAAGTGATT[A/C/G]ACCTGCCTCAGCCTC | 51096 |
rs577271795 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51260960 | CGCGGGCTGGGCGCA[C/G]TCGGGCGGGGCGCGC | 51096 |
rs577333116 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51261411 | ATTCCGTTCATTTAG[C/T]AAATATTGGTGAACC | 51096 |
rs577339448 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51279105 | AAAATTTTAAAAATA[C/T]AGACATATATTTTTG | 51096 |
rs577356289 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UTP18 | GRCh38.p7 | 17:51262662 | AAGTGATCCTCCTGC[C/G]TCTGCCTCCCAAGTA | 51096 |
rs577400372 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51272559 | ATGAAAAATAATGTA[G/T]ATTAATTAGATCTAG | 51096 |
rs577578667 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51268261 | TCAATCTCCTGACCT[C/T]GTGATCCGCCCGCCT | 51096 |
rs577580291 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51274713 | CGCCTCAGCTCCCAA[A/C]GTGCTGGGATTACAG | 51096 |
rs577583475 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | UTP18 | GRCh38.p7 | 17:51289174 | TGCAGTGGCCACCCT[C/T]GTAAGCAGACCTTTC | 51096 |
rs577603347 | snp | G/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51272076 | TCATTCTTAAATATA[G/T]TAAACATAGTTTTTT | 51096 |
rs577640949 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51282028 | CTGTCCTGCTCTTCT[A/G]CCTTTCTGACTTCCC | 51096 |
rs577643526 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51268577 | GACAACCATGTAACT[A/G]GATGGAAATAATTAA | 51096 |
rs577664501 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | UTP18 | GRCh38.p7 | 17:51281092 | CTGAGGCAAAGAATC[A/T]CTTGAACCTGGGAGA | 51096 |
rs577708924 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UTP18 | GRCh38.p7 | 17:51282738 | GAGATCTAATTTATC[A/G]TAAGGTCCTAAGAAA | 51096 |
rs577740245 | snp | C/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51281435 | TTTTTTCTCTATTCT[C/G]TCTTTTGTCACTTGG | 51096 |
rs577840362 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UTP18 | GRCh38.p7 | 17:51263501 | AGATTTGAAAAATAT[C/T]TGAAAGTATAGAAAA | 51096 |
rs577856261 | snp | C/T | | | upstream-variant-2KB, utr-variant-5-prime | UTP18, MBTD1 | GRCh38.p7 | 17:51260321 | GTTGCAGCTGCGAAA[C/T]TGTGTTGGAAAAATT | 51096 |
rs577934669 | snp | A/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51296772 | GTAAGCCTACTCATG[A/T]TACCTAAAATCTGAG | 51096 |
rs577942988 | snp | C/G | 0.000558295 | 0.0166984 | intron-variant | UTP18 | GRCh38.p7 | 17:51286480 | TTCACTCTCTCCTTC[C/G]AGGTTAAAACTGGGG | 51096 |
rs577967812 | snp | C/T | | | intron-variant, downstream-variant-500B | UTP18 | GRCh38.p7 | 17:51289282 | GCTCACTGCAGCCTC[C/T]GCCTCCTGGGTTCAA | 51096 |
rs577990585 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51280757 | GACAGAGGTTGCAGT[A/G]AGCTGTGATTGGGCC | 51096 |
rs578223227 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UTP18 | GRCh38.p7 | 17:51271660 | ATCTATTGGAGGCTT[A/T]ATTTAATTTTATTTG | 51096 |
rs578261636 | snp | C/G | 0.0267878 | 0.112589 | intron-variant, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51260994 | GGGCGGTGAAGCTCC[C/G]GGGGGCGGAGCCTGG | 51096 |
rs745341287 | snp | C/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51282356 | TGTCCTAGAATCAGA[C/T]TTTCACAAGGTTATT | 51096 |
rs745344126 | snp | A/G | | | utr-variant-3-prime | UTP18 | GRCh38.p7 | 17:51297808 | TCACAAGAGAAGCCT[A/G]TCTTGATATATCATC | 51096 |
rs745375002 | snp | A/G | 4.12014e-05 | 0.00453861 | synonymous-codon, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51260665 | GCCCGGAATGAGGCC[A/G]GACTGGAAAGCCGGA | 51096 |
rs745388460 | snp | G/T | 1.66145e-05 | 0.00288218 | synonymous-codon | UTP18 | GRCh38.p7 | 17:51275940 | GCAGTTCCATCCCGG[G/T]GCACAGATTGTGATG | 51096 |
rs745443707 | snp | C/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51283870 | GCCACCTGCCTTGGC[C/T]TCCCAAAGTGCTGGG | 51096 |
rs745460298 | snp | G/T | | | intron-variant, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51262225 | TAGCTGGCATTACAG[G/T]CGTGCGCCACCACGC | 51096 |
rs745487528 | snp | A/G | 5.06086e-05 | 0.00503008 | synonymous-codon | UTP18 | GRCh38.p7 | 17:51288077 | AGATTCTTGTCTCCA[A/G]GAAACAAACCCAAAG | 51096 |
rs745563374 | snp | C/G | 1.7074e-05 | 0.00292177 | intron-variant | UTP18 | GRCh38.p7 | 17:51275845 | TTCAATTGATAAAAT[C/G]CCAGCTTTCATTTCC | 51096 |
rs745567810 | in-del | -/TATATT | | | intron-variant | UTP18 | GRCh38.p7 | 17:51295853 | CACCTGGGGAATATA[-/TATATT]TATATTTTTTGGAAA | 51096 |
rs745694851 | snp | A/G | 0.000186829 | 0.0096633 | intron-variant | UTP18 | GRCh38.p7 | 17:51286448 | GTCCAGAAACTTAGC[A/G]TACTCTCTACTCTTT | 51096 |
rs745715271 | snp | C/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51263797 | ACTTTTAGCACAGTG[C/T]CTGAAACTGAGTAAA | 51096 |
rs745899051 | snp | A/C | 3.34174e-05 | 0.00408749 | intron-variant | UTP18 | GRCh38.p7 | 17:51296930 | CTGTGGGTAATTACA[A/C]AGTTGTTCAGATGAC | 51096 |
rs745904625 | in-del | -/GAA | 1.67239e-05 | 0.00289166 | cds-indel | UTP18 | GRCh38.p7 | 17:51275868 | TCATTTCCTATAGAT[-/GAA]GAACTGCCAGCATGC | 51096 |
rs745926338 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51279106 | AAATTTTAAAAATAT[A/G]GACATATATTTTTGA | 51096 |
rs745964920 | snp | A/G | 0.000171482 | 0.00925807 | intron-variant | UTP18 | GRCh38.p7 | 17:51297757 | CTATAAATCAGGTAT[A/G]TAATTTCTTTTGTTC | 51096 |
rs745975779 | snp | A/G | 1.66452e-05 | 0.00288484 | intron-variant | UTP18 | GRCh38.p7 | 17:51277327 | TTCTGTTGAATGCAC[A/G]CAACCAGTCATTCCC | 51096 |
rs745981329 | snp | C/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51267543 | TTTGCATTTCCTCTT[C/T]CCTCAATCTGATTAT | 51096 |
rs746038198 | snp | C/G | 0.000113684 | 0.0075385 | missense, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51260587 | CTCAAACCTAACGAT[C/G]CCGCCGGAGCGGAGG | 51096 |
rs746040254 | in-del | -/TT | | | intron-variant | UTP18 | GRCh38.p7 | 17:51282876 | CTTCTTCTTTTTTTT[-/TT]TTTTTTTTTGAGACA | 51096 |
rs746051966 | in-del | -/C | 1.75305e-05 | 0.00296056 | frameshift-variant | UTP18 | GRCh38.p7 | 17:51288056 | AGTGGTAAATATATA[-/C]AATCAAGATTCTTGT | 51096 |
rs746100556 | in-del | -/AG | | | intron-variant | UTP18 | GRCh38.p7 | 17:51270685 | CTTATAGGAGGAGAA[-/AG]AGGGGATTTTTATTG | 51096 |
rs746172837 | in-del | -/AA | | | upstream-variant-2KB, intron-variant | UTP18, MBTD1 | GRCh38.p7 | 17:51259506 | GGTGGCTAAAAAAGG[-/AA]AAGTCTCGGATCCAG | 51096 |
rs746218977 | snp | C/T | 1.67539e-05 | 0.00289425 | intron-variant | UTP18 | GRCh38.p7 | 17:51268943 | AATTAGTACATAAGT[C/T]CCTGTTCCTGTTCGT | 51096 |
rs746235516 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51291202 | AGTTAAAGAAGTTGG[A/G]TCTTTATAGGCATTT | 51096 |
rs746298073 | snp | A/G | | | intron-variant, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51261611 | AATCCCTGCCTTTTG[A/G]CGCTTGTGTGCTAGT | 51096 |
rs746307273 | snp | C/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51277969 | AGTGTTGGCGTATGG[C/T]ACGGCTCACTGGTGC | 51096 |
rs746348768 | snp | C/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51291876 | TGGTGAGTGAATGCC[C/T]GAGGCCTAGTTTCAT | 51096 |
rs746350811 | snp | A/G | 3.44039e-05 | 0.00414738 | intron-variant | UTP18 | GRCh38.p7 | 17:51280488 | TCTTCGGGTAAGACA[A/G]CGACATGAAAGAAGC | 51096 |
rs746419273 | snp | A/G | 3.3123e-05 | 0.00406945 | missense | UTP18 | GRCh38.p7 | 17:51285250 | TTTTATGCAGGGGAT[A/G]GAGAAGTTTATGTTT | 51096 |
rs746466329 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51293771 | CTTTGCTGCACTAAT[A/G]GACTGTACTTTCTTG | 51096 |
rs746546839 | snp | C/T | 0.000125894 | 0.00793293 | missense, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51260838 | TGGAGGAGGACAAAC[C/T]GGCCGTGGAGCGGTG | 51096 |
rs746571682 | in-del | -/TCTCACTCTGTCACCCAGGGCTGGAGTGCAGTGAC | | | intron-variant | UTP18 | GRCh38.p7 | 17:51269881 | GTGTCAGTGTCAGAA[lengthTooLong]TCTCACTCTGTCACC | 51096 |
rs746584037 | snp | C/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51296642 | TTTCCACCAGAGCAT[C/T]GCTCTTTAGAATGAC | 51096 |
rs746599374 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51283487 | TTCTTATTCTGTATG[A/G]AGTCGTTTGTGTGAT | 51096 |
rs746602047 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51282247 | GGAGCATTTGGTAAT[A/G]TAACATTAATAAAAT | 51096 |
rs746639476 | snp | A/G | 3.56163e-05 | 0.00421982 | intron-variant | UTP18 | GRCh38.p7 | 17:51275998 | CTATTTCAGGTATGC[A/G]TCTTTATTTACTTAT | 51096 |
rs746727652 | snp | C/T | 4.96915e-05 | 0.0049843 | synonymous-codon | UTP18 | GRCh38.p7 | 17:51277189 | AAGGTTTCCAATCTT[C/T]AAGGCTTGTTTTAGT | 51096 |
rs746778660 | snp | G/T | | | intron-variant, missense | UTP18 | GRCh38.p7 | 17:51286553 | AGTTTGGGAGGAAAG[G/T]CAAGTAGAACTAGGC | 51096 |
rs746865965 | snp | G/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51273242 | CTTTAAAAAAAGCAA[G/T]TGAGGTAGGGAGGCT | 51096 |
rs746896291 | snp | G/T | 1.82071e-05 | 0.00301716 | intron-variant | UTP18 | GRCh38.p7 | 17:51266154 | ACTCTTTAAAAGTTA[G/T]TTAAAATATGCTGTT | 51096 |
rs746930118 | snp | A/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51263681 | AGTTTCTAATTGACC[A/T]TGGGCAGTTTGGAAC | 51096 |
rs747059447 | snp | A/G/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51291136 | CGGTGGCTCACGCCT[A/G/T]TAATCCCAGCACTTT | 51096 |
rs747065361 | snp | A/T | 1.89561e-05 | 0.00307858 | intron-variant | UTP18 | GRCh38.p7 | 17:51280340 | TCTACATTGTGTGAT[A/T]CTTCTGTATACTTTC | 51096 |
rs747087948 | snp | A/C | 1.65688e-05 | 0.00287821 | synonymous-codon | UTP18 | GRCh38.p7 | 17:51263336 | AAAAGGTAATTTTCC[A/C]CCTCAAAAGAAGCCA | 51096 |
rs747101443 | snp | C/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51276513 | GTTATTAGAGCAAAG[C/T]GATAATATAACCTCA | 51096 |
rs747102024 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51277601 | TGCAGCAGAAAAAGC[A/G]TGAGCCATGGAGCTA | 51096 |
rs747145334 | in-del | -/A | 5.19404e-05 | 0.00509583 | intron-variant | UTP18 | GRCh38.p7 | 17:51293871 | GAGCTCCCAGTTGTT[-/A]ACACTTTAAAGTTTT | 51096 |
rs747153165 | snp | C/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51266816 | TGTTAGTTTCTCCAA[C/T]TGTTGTAAGGTGCAT | 51096 |
rs747156862 | snp | C/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51265654 | TTTCAACCTCTGCCT[C/T]CTGGGTTCAAGTGGT | 51096 |
rs747312037 | snp | A/C | 1.71823e-05 | 0.00293101 | synonymous-codon | UTP18 | GRCh38.p7 | 17:51280045 | CTTTGAAGTCTCCCC[A/C]GATGGGTCCTTCTTG | 51096 |
rs747351139 | snp | C/G/T | 3.65292e-05 | 0.00427358 | missense, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51260621 | CGAATGAAACTGGAC[C/G/T]GGAGAACCGGAGCGA | 51096 |
rs747442553 | snp | A/G | | | upstream-variant-2KB, intron-variant | UTP18, MBTD1 | GRCh38.p7 | 17:51258944 | AAAATATAGGCCAAT[A/G]AGCAGTGGGTGGGTG | 51096 |
rs747476399 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51290026 | ATGGCATGTAGGGCA[A/G]GGAGGAGGCTAAGCT | 51096 |
rs747498769 | snp | C/G | 1.65798e-05 | 0.00287917 | intron-variant | UTP18 | GRCh38.p7 | 17:51285378 | TTGTGGGTAAGTAAA[C/G]AGAGGTTCTTGTAAC | 51096 |
rs747532121 | snp | C/G | 1.69029e-05 | 0.00290709 | intron-variant | UTP18 | GRCh38.p7 | 17:51268953 | TAAGTCCCTGTTCCT[C/G]TTCGTTATTATTTGA | 51096 |
rs747539614 | snp | A/G | 1.65894e-05 | 0.00288 | missense | UTP18 | GRCh38.p7 | 17:51273382 | AGTGAAGAGGATGAA[A/G]ATGATTTGTTGCAAA | 51096 |
rs747647220 | snp | A/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51281203 | TTTGGTTTTAAAGTT[A/T]CTTTTTAGCTAGAAA | 51096 |
rs747652638 | in-del | -/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51274624 | TTTTTTTTGTTTTTG[-/T]TTTTTTTGGTAGAGA | 51096 |
rs747731448 | snp | C/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51262513 | CAGACTGGAGTGTAG[C/T]GGCACCTATTAGTCT | 51096 |
rs747732679 | snp | C/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51279431 | TTTGGTTACATGTGT[C/G]ACATCCAGAGAAGCT | 51096 |
rs747753017 | snp | C/T | 3.90373e-05 | 0.00441782 | missense, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51260849 | AAACCGGCCGTGGAG[C/T]GGTGCTTGGAGGAGC | 51096 |
rs747759003 | snp | C/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51293532 | AAGCTCATCACCTGT[C/T]GTTAGTGTTAGTGTA | 51096 |
rs747840629 | snp | C/T | 1.69115e-05 | 0.00290782 | missense, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51260904 | ACGAGGACGCGTTGC[C/T]GCGGCGTCTGCGAGG | 51096 |
rs747939454 | snp | A/G | | | intron-variant, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51261367 | CCCATGTGACTATGA[A/G]ACCCACCATGTTTTG | 51096 |
rs747966612 | snp | C/G/T | 0.000372926 | 0.01365 | intron-variant | UTP18 | GRCh38.p7 | 17:51286455 | AACTTAGCATACTCT[C/G/T]TACTCTTTGTTCACT | 51096 |
rs747983907 | snp | A/T | 3.31268e-05 | 0.00406968 | missense | UTP18 | GRCh38.p7 | 17:51277201 | CTTTAAGGCTTGTTT[A/T]AGTGCTAATGGGGAA | 51096 |
rs748007273 | snp | A/G | 7.22256e-05 | 0.00600896 | intron-variant | UTP18 | GRCh38.p7 | 17:51293859 | ATTTAAGAAACATGA[A/G]CTCCCAGTTGTTACA | 51096 |
rs748009097 | in-del | -/TTC | | | intron-variant | UTP18 | GRCh38.p7 | 17:51275662 | GATGGTAAAAATGGA[-/TTC]TTTTGTGGTAAAGTG | 51096 |
rs748027221 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime, intron-variant, nc-transcript-variant | UTP18, MBTD1 | GRCh38.p7 | 17:51260034 | ACTCGGGTGGCCCCA[A/G]GATATCAACAACATT | 51096 |
rs748031155 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51285479 | TTTATAAACTATTCA[A/G]TAATATGAAATTGGT | 51096 |
rs748071009 | in-del | -/TT | 1.67192e-05 | 0.00289125 | intron-variant | UTP18 | GRCh38.p7 | 17:51296924 | AAACACTGTGGGTAA[-/TT]TTACAAAGTTGTTCA | 51096 |
rs748096404 | snp | A/G | 3.77644e-05 | 0.0043452 | intron-variant | UTP18 | GRCh38.p7 | 17:51276016 | TTTATTTACTTATTT[A/G]TTTCTAATGCATTAT | 51096 |
rs748227261 | snp | C/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51288371 | TGTTGGAAGGATGCA[C/T]AGTAGCCACCACATT | 51096 |
rs748279347 | snp | C/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51276290 | ACCATCCCTTGCCCA[C/T]TCACATTTTTATTGA | 51096 |
rs748383127 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51264824 | AGTAGCTGGGACTAC[A/G]GGCACATGTCACCAT | 51096 |
rs748470469 | snp | C/T | 1.74406e-05 | 0.00295296 | intron-variant | UTP18 | GRCh38.p7 | 17:51266166 | TTATTTAAAATATGC[C/T]GTTCTGTTTTTGTAG | 51096 |
rs748477703 | snp | C/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51295552 | CTGTTCTGTTCCATT[C/G]GTCTATATCTCTGTT | 51096 |
rs748489126 | snp | A/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51280838 | TTTTTTTTTTAGCCA[A/T]CTATCCTGGGCGACA | 51096 |
rs748618939 | snp | A/G | 1.73075e-05 | 0.00294167 | intron-variant | UTP18 | GRCh38.p7 | 17:51275834 | TGTTTATTCATTTCA[A/G]TTGATAAAATCCCAG | 51096 |
rs748652376 | in-del | -/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51292280 | AGTGAAGTCCAAATT[-/G]GGGGTACTGCCAACT | 51096 |
rs748784742 | snp | C/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51285152 | TGTATTTGTAGTCTC[C/T]TGTACTGTTAAGAGG | 51096 |
rs748811424 | snp | C/G | 1.65798e-05 | 0.00287917 | missense | UTP18 | GRCh38.p7 | 17:51273398 | ATGATTTGTTGCAAA[C/G]GACTGGGAATTTCAT | 51096 |
rs748838246 | snp | A/G | 1.76347e-05 | 0.00296935 | missense | UTP18 | GRCh38.p7 | 17:51288053 | TGGAGTGGTAAATAT[A/G]TACAATCAAGATTCT | 51096 |
rs748905209 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51266309 | TTCATATGATTTACC[A/G]AGAGGTGTATGTAAC | 51096 |
rs748922400 | snp | A/G | | | intron-variant, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51261734 | TGGGCGTGTGTAGAG[A/G]CCTGTGAAATTTTAG | 51096 |
rs748922412 | snp | C/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51291265 | AATGGGGGCTATAAA[C/T]AGATGTCAGAGCACA | 51096 |
rs748955900 | snp | A/T | 1.66109e-05 | 0.00288187 | intron-variant | UTP18 | GRCh38.p7 | 17:51285410 | TTAATCACATTGTGC[A/T]AATGAGAATATGTTG | 51096 |
rs749123604 | snp | A/G | | | downstream-variant-500B | UTP18 | GRCh38.p7 | 17:51298005 | CATTTAAGACTAAAC[A/G]TGAGAAATTGGAAAC | 51096 |
rs749142781 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51280605 | GATCACTTGAGGTCA[A/G]CGGGTAAGATCAGCC | 51096 |
rs749159468 | snp | A/G | 1.65622e-05 | 0.00287764 | missense | UTP18 | GRCh38.p7 | 17:51277217 | AGTGCTAATGGGGAA[A/G]AAGTTTTAGCCACGA | 51096 |
rs749218608 | snp | A/G | 1.68678e-05 | 0.00290407 | missense | UTP18 | GRCh38.p7 | 17:51294044 | AAGGCCCTGATGTAT[A/G]GGTAGGTATTATTTA | 51096 |
rs749250452 | snp | A/G | 0.000441452 | 0.0148503 | synonymous-codon, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51260863 | GCGGTGCTTGGAGGA[A/G]CTGGTCTTCGGCGAC | 51096 |
rs749316959 | snp | G/T | 1.6599e-05 | 0.00288084 | splice-donor-variant | UTP18 | GRCh38.p7 | 17:51277305 | TGCATCAAGTGAGAG[G/T]TAAGATTTCTGTTGA | 51096 |
rs749340207 | snp | A/C/T | 9.59676e-05 | 0.00692649 | utr-variant-5-prime, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51260583 | TCTCCTCAAACCTAA[A/C/T]GATGCCGCCGGAGCG | 51096 |
rs749387063 | snp | A/G | | | intron-variant, missense | UTP18 | GRCh38.p7 | 17:51286634 | GATCCCTTGGAGGGA[A/G]AGTGCCCTGATGAAG | 51096 |
rs749415209 | snp | A/T | 3.33378e-05 | 0.00408262 | missense | UTP18 | GRCh38.p7 | 17:51293953 | CCCAGTCATTAAAAA[A/T]AAGAATATTTCTCAT | 51096 |
rs749474853 | snp | C/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51287940 | GATTCCTGTAAATAC[C/G]AGTTTGTGGGGTTAA | 51096 |
rs749489154 | snp | C/T | 1.97404e-05 | 0.00314163 | intron-variant | UTP18 | GRCh38.p7 | 17:51266332 | TATGTAACCAATGCC[C/T]AGTCATTAACCGTAA | 51096 |
rs749584544 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51291902 | TTCATAGTATCAGGT[A/G]AATAGGGTGGGAACA | 51096 |
rs749591824 | snp | C/T | 2.40851e-05 | 0.00347015 | utr-variant-5-prime, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51260549 | ATGCGCAGCGAGGTT[C/T]CACGTGAGCGCCTGC | 51096 |
rs749659555 | snp | G/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51290128 | TCCTTAAGAAATGTT[G/T]TGTTGCGCTGGGCAC | 51096 |
rs749662279 | snp | C/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51279215 | CTCCCTGTCTTCCTG[C/T]TTTCCTTCCTTGGAG | 51096 |
rs749716248 | in-del | -/AT | 6.75573e-05 | 0.00581155 | intron-variant | UTP18 | GRCh38.p7 | 17:51273325 | AGGGGCAGCTCATTG[-/AT]TCTAAAGATCAGCCT | 51096 |
rs749736401 | snp | G/T | | | missense | UTP18 | GRCh38.p7 | 17:51280408 | AAGAACTGATTGGAA[G/T]CATGAAAATTAATGG | 51096 |
rs749813973 | snp | C/T | 4.99397e-05 | 0.00499673 | intron-variant | UTP18 | GRCh38.p7 | 17:51268910 | TCTTCAGATGGTGAG[C/T]GTTGATATTTCTGTT | 51096 |
rs749853919 | snp | C/T | 3.55385e-05 | 0.00421521 | intron-variant | UTP18 | GRCh38.p7 | 17:51280380 | GATAAATAATATTTA[C/T]TGTTTTAGACCAAAG | 51096 |
rs749879591 | in-del | -/G | 0.000256443 | 0.0113206 | intron-variant, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51260948 | GAGGCCGCGGCGCGC[-/G]GGCTGGGCGCACTCG | 51096 |
rs749900292 | snp | A/C/G | 8.55055e-05 | 0.00653808 | utr-variant-5-prime, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51260565 | CACGTGAGCGCCTGC[A/C/G]TTTCTCCTCAAACCT | 51096 |
rs749938766 | snp | C/G | 1.69565e-05 | 0.00291169 | missense | UTP18 | GRCh38.p7 | 17:51293903 | TATTATCTCCTGCAG[C/G]TTCATCTTCCTTCCT | 51096 |
rs749965965 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51291299 | TAGTTTTAATCAGGT[A/G]AGATCATTGGCTTGA | 51096 |
rs749993643 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51267166 | ATGAGGTTTTTCGCC[A/G]TGTCGCCCAGGCTGG | 51096 |
rs750056521 | in-del | -/CTT | 1.72264e-05 | 0.00293477 | cds-indel | UTP18 | GRCh38.p7 | 17:51280054 | CTCCCCAGATGGGTC[-/CTT]CTTGCTCATAAATGG | 51096 |
rs750113590 | snp | A/C | | | intron-variant | UTP18 | GRCh38.p7 | 17:51286334 | AATTCTGTAACTTCA[A/C]GAAGTAGGTTTTTGT | 51096 |
rs750130985 | snp | A/C | 7.28797e-05 | 0.0060361 | intron-variant | UTP18 | GRCh38.p7 | 17:51288222 | AATATTTCATTACCC[A/C]TTTATTATTGTTATT | 51096 |
rs750251250 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51290640 | AAAACCATGGGATCT[A/G]TCTCCTGTTGACATA | 51096 |
rs750252362 | snp | A/G | 2.21944e-05 | 0.00333117 | intron-variant | UTP18 | GRCh38.p7 | 17:51263437 | ACACTTAAAAAAGTT[A/G]TTTTGCAGATTTTAA | 51096 |
rs750254541 | snp | A/G | 1.68111e-05 | 0.00289918 | missense | UTP18 | GRCh38.p7 | 17:51280419 | GGAAGCATGAAAATT[A/G]ATGGAAGGGTTGCAG | 51096 |
rs750296742 | snp | C/T | 3.48038e-05 | 0.00417141 | missense, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51260721 | AGCCTGCCCCTTCAT[C/T]CCAGCGGAAACCGCC | 51096 |
rs750311189 | snp | C/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51276997 | GATTAAATCACTGGC[C/T]GTGGCTGCTTAAGTC | 51096 |
rs750366224 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51278425 | TTTCACTATTCAAAA[A/G]TAATGGATTCTGGCA | 51096 |
rs750366248 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51266629 | TCATATTTGCTTTGT[A/G]TATTTGGGGGATGTG | 51096 |
rs750622457 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51268522 | AAGAGACTTCTTTAC[A/G]TAGTCCTGATATCTG | 51096 |
rs750654357 | snp | A/C | 3.4181e-05 | 0.00413393 | intron-variant | UTP18 | GRCh38.p7 | 17:51273483 | TGGGGGATCCTATCT[A/C]ACTACTTACCTCTGC | 51096 |
rs750677698 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51269719 | AAGTAGAAATTGACC[A/G]TCTTTGTTTCTAGCC | 51096 |
rs750794273 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51275608 | TTCAGACTTCTAGAT[A/G]TGGAAAGCACTTTAA | 51096 |
rs750803221 | snp | A/G | 1.65633e-05 | 0.00287774 | missense | UTP18 | GRCh38.p7 | 17:51285350 | CCACATCTAGGAATG[A/G]ACAGTATGTTGCTTG | 51096 |
rs750859051 | snp | A/G | 3.9816e-05 | 0.00446166 | synonymous-codon, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51260899 | GAACGACGAGGACGC[A/G]TTGCTGCGGCGTCTG | 51096 |
rs750894368 | snp | C/T | 6.53531e-05 | 0.00571597 | intron-variant | UTP18 | GRCh38.p7 | 17:51279988 | ACTTTATTTAATTGC[C/T]TCATTTCCTATTTTA | 51096 |
rs750926492 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51263175 | TCATCAGAGAGTGGT[A/G]GAAAAAACATTCTAT | 51096 |
rs751070945 | in-del | -/T | 1.82088e-05 | 0.00301729 | intron-variant | UTP18 | GRCh38.p7 | 17:51280520 | AAGGATATTTTTACA[-/T]TTTAAATTTTAGGCC | 51096 |
rs751085444 | snp | C/T | 1.6574e-05 | 0.00287867 | missense | UTP18 | GRCh38.p7 | 17:51277286 | GCTGGAAAGTTAATT[C/T]CTGTGCATCAAGTGA | 51096 |
rs751135329 | snp | G/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51297645 | TTTTTAAAGGTACAG[G/T]CATTTTGGGCAAAGC | 51096 |
rs751144769 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51264403 | ATCACCTCTTTATGT[A/G]TAAACCTTTCTTTAT | 51096 |
rs751189534 | snp | A/T | 3.37416e-05 | 0.00410727 | synonymous-codon | UTP18 | GRCh38.p7 | 17:51293911 | CCTGCAGGTTCATCT[A/T]CCTTCCTGTACAGTA | 51096 |
rs751192829 | snp | C/G/T | 8.15719e-05 | 0.00638596 | utr-variant-5-prime, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51260571 | AGCGCCTGCGTTTCT[C/G/T]CTCAAACCTAACGAT | 51096 |
rs751281507 | snp | G/T | 3.32579e-05 | 0.00407773 | missense | UTP18 | GRCh38.p7 | 17:51294007 | GAGAAGTGGATACTT[G/T]GCCTTGGGGAATGAA | 51096 |
rs751299041 | snp | C/T | 1.65965e-05 | 0.00288062 | missense | UTP18 | GRCh38.p7 | 17:51268886 | GCAGAGACTACTAAG[C/T]GGAAAACATCTTCAG | 51096 |
rs751389351 | snp | G/T | 4.96611e-05 | 0.00498278 | upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51260535 | AGGGGCCTGGGCGCA[G/T]GCGCAGCGAGGTTCC | 51096 |
rs751418279 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51287856 | TGAATTCTGTTTTCA[A/G]CCTGTTTGGTTGGAG | 51096 |
rs751434838 | snp | C/T | | | intron-variant, downstream-variant-500B | UTP18 | GRCh38.p7 | 17:51289451 | CGACCTCATGGTCCA[C/T]CTGCCTCGGGCTCCC | 51096 |
rs751466028 | snp | A/C | 1.68434e-05 | 0.00290197 | missense | UTP18 | GRCh38.p7 | 17:51280459 | TCTCTTCAGATAGTA[A/C]GAAAGTATACGCCTC | 51096 |
rs751492426 | snp | C/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51291146 | CGCCTGTAATCCCAG[C/T]ACTTTGTGAGGCCGA | 51096 |
rs751492769 | snp | A/G | 5.36533e-05 | 0.00517917 | intron-variant | UTP18 | GRCh38.p7 | 17:51280517 | GCTAAGGATATTTTT[A/G]CATTTTAAATTTTAG | 51096 |
rs751517440 | snp | C/T | | | intron-variant, downstream-variant-500B | UTP18 | GRCh38.p7 | 17:51289458 | ATGGTCCACCTGCCT[C/T]GGGCTCCCAAAGTGC | 51096 |
rs751525371 | snp | C/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51276153 | GACAGAGTTCATTTA[C/T]TTGGAAATACAAAAC | 51096 |
rs751654575 | snp | A/G | 1.6972e-05 | 0.00291303 | synonymous-codon, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51260791 | GGCGGCGGAGGAAGA[A/G]AGACGGCTCCGGCAG | 51096 |
rs751666487 | snp | A/C | | | intron-variant | UTP18 | GRCh38.p7 | 17:51285043 | TCCAGCCTGGGCGAC[A/C]AGAGAAAAACTGCAT | 51096 |
rs751694361 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime, intron-variant | UTP18, MBTD1 | GRCh38.p7 | 17:51259156 | ACCACTTGTCAGAGA[A/G]GCTGCAGAGGGGACG | 51096 |
rs751695093 | snp | A/G | | | intron-variant, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51262009 | CTAGTAGTAGAGCAA[A/G]TAGAAACCACTTGGA | 51096 |
rs751753379 | snp | C/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51291793 | ATAGAAAGGTTGGTT[C/T]TAGTGTATTTTGATG | 51096 |
rs751779835 | snp | C/G | 4.17982e-05 | 0.00457136 | synonymous-codon, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51260737 | CCAGCGGAAACCGCC[C/G]GCCCGGCCGAGCGCG | 51096 |
rs751786555 | snp | C/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51278888 | ATTGGAAATGTAGTA[C/T]GTGTCTGAAATAATA | 51096 |
rs751792481 | snp | C/T | 4.98136e-05 | 0.00499042 | missense | UTP18 | GRCh38.p7 | 17:51275896 | CATGCGAATGCTGAA[C/T]GTCCTACTGTTGCTC | 51096 |
rs751817762 | snp | C/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51267295 | TGTTCAGACCTGTTG[C/T]CTTGTAGAATATCCC | 51096 |
rs751857144 | snp | A/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51279737 | GATATGTTTACTGTT[A/T]GGAGAGCTGAGTCTC | 51096 |
rs751990008 | snp | A/G | 1.69533e-05 | 0.00291142 | synonymous-codon | UTP18 | GRCh38.p7 | 17:51288188 | TTCAGAAAAAATGAA[A/G]GAAGCAGTCAGATTG | 51096 |
rs751990181 | snp | A/G | 1.74903e-05 | 0.00295717 | intron-variant | UTP18 | GRCh38.p7 | 17:51275820 | TCTAAAGAAAATAAT[A/G]TTTATTCATTTCAAT | 51096 |
rs751997503 | snp | C/T | 1.76899e-05 | 0.00297399 | intron-variant | UTP18 | GRCh38.p7 | 17:51263405 | AGTTGCCTAACTTTT[C/T]TTCTGAATCCCTCTG | 51096 |
rs752011271 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51271768 | TGCCTCCTGAGTTCA[A/G]ATGATTCTCCTGCCT | 51096 |
rs752063529 | snp | A/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51272524 | CCTGGTTATATTTCA[A/T]TGAGTGGTGGACATT | 51096 |
rs752178671 | in-del | -/GTACTTCAGTCTGGG | | | intron-variant | UTP18 | GRCh38.p7 | 17:51271582 | GTCTGGGTATATTTT[-/GTACTTCAGTCTGGG]TCTGATTCGTTTTCT | 51096 |
rs752180206 | snp | A/G | 1.90914e-05 | 0.00308956 | missense | UTP18 | GRCh38.p7 | 17:51288037 | TTTGTAGTTCTAATT[A/G]TGGAGTGGTAAATAT | 51096 |
rs752190078 | snp | C/T | 3.31323e-05 | 0.00407002 | missense | UTP18 | GRCh38.p7 | 17:51263293 | AAGAACATGAAGACT[C/T]GGGTGACTCAGAAGT | 51096 |
rs752238123 | snp | A/G | 3.44104e-05 | 0.00414777 | intron-variant | UTP18 | GRCh38.p7 | 17:51275838 | TATTCATTTCAATTG[A/G]TAAAATCCCAGCTTT | 51096 |
rs752327216 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51274313 | CACTATGTCTAGCAT[A/G]TTCATTATGGTAACC | 51096 |
rs752348704 | snp | G/T | 1.672e-05 | 0.00289132 | intron-variant | UTP18 | GRCh38.p7 | 17:51297022 | AGAAAACCCTTTTCT[G/T]ACAAATTCTGCAGGT | 51096 |
rs752371408 | snp | C/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51270207 | TTAGACAGTTTTTCC[C/T]ATTTTGAAATGTATG | 51096 |
rs752421820 | snp | C/G/T | 7.31093e-05 | 0.00604566 | missense, stop-gained, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51260606 | CCGGAGCGGAGGAGA[C/G/T]GAATGAAACTGGACC | 51096 |
rs752435025 | snp | A/G | 9.65801e-05 | 0.00694843 | intron-variant | UTP18 | GRCh38.p7 | 17:51279998 | ATTGCTTCATTTCCT[A/G]TTTTAGGTTTGAAAG | 51096 |
rs752497584 | snp | A/C | | | intron-variant | UTP18 | GRCh38.p7 | 17:51268432 | ATAATGAAGTTTTGT[A/C]TATTCTTAACAATCT | 51096 |
rs752580229 | snp | C/T | 1.65611e-05 | 0.00287755 | missense | UTP18 | GRCh38.p7 | 17:51285302 | GCCTTAACAGATTTG[C/T]TGATGAAGGCAGTTT | 51096 |
rs752601761 | in-del | -/TT/TTT | | | intron-variant | UTP18 | GRCh38.p7 | 17:51265562 | CCACCGTGCCCGGCC[-/TT/TTT]TTTTTTTTTTTTTTT | 51096 |
rs752616093 | snp | C/G | 5.05702e-05 | 0.00502817 | intron-variant | UTP18 | GRCh38.p7 | 17:51273333 | CTCATTGATTCTAAA[C/G]ATCAGCCTTCTGGGT | 51096 |
rs752673957 | in-del | -/CAA | | | upstream-variant-2KB, cds-indel, intron-variant, nc-transcript-variant | UTP18, MBTD1 | GRCh38.p7 | 17:51260040 | GTGGCCCCAGGATAT[-/CAA]CAACATTAGCATAGC | 51096 |
rs752698375 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51287559 | TCATTGAAGGGAGGC[A/G]GGAGGAGGGGTGATG | 51096 |
rs752729183 | snp | C/G | 1.95105e-05 | 0.00312328 | utr-variant-5-prime, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51260579 | CGTTTCTCCTCAAAC[C/G]TAACGATGCCGCCGG | 51096 |
rs752755264 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51292171 | TCTCTGTAAAACAGG[A/G]GTCTGCTTTTTTACT | 51096 |
rs752781542 | snp | C/T | | | upstream-variant-2KB, utr-variant-5-prime | UTP18, MBTD1 | GRCh38.p7 | 17:51260139 | CTCTCTCGCTTCCAC[C/T]GTGGGACCCTCTGCA | 51096 |
rs752828106 | snp | A/C | | | intron-variant | UTP18 | GRCh38.p7 | 17:51279839 | CTTATGTTTGGGTCA[A/C]ACTCAGTGATGCCTG | 51096 |
rs752926608 | snp | C/T | 5.59331e-05 | 0.00528805 | missense, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51260798 | GAGGAAGAGAGACGG[C/T]TCCGGCAGCGGAACC | 51096 |
rs752935570 | snp | C/T | | | intron-variant, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51261387 | ACCATGTTTTGAGAA[C/T]GATCGTGTATTCCGT | 51096 |
rs752978730 | snp | A/G | | | missense | UTP18 | GRCh38.p7 | 17:51277233 | AAGTTTTAGCCACGA[A/G]TACCCACAGCAAGGT | 51096 |
rs753034234 | snp | G/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51296305 | TATGTTTGTATGCTT[G/T]AGGGAATTCCTGCTT | 51096 |
rs753119136 | snp | A/C | 1.76403e-05 | 0.00296982 | intron-variant | UTP18 | GRCh38.p7 | 17:51288214 | GATTGGTAAATATTT[A/C]ATTACCCCTTTATTA | 51096 |
rs753123923 | snp | C/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51297459 | CCCAATATTTAAAAC[C/G]ATAGAACATCCTTCC | 51096 |
rs753124534 | snp | C/T | 1.66843e-05 | 0.00288823 | intron-variant | UTP18 | GRCh38.p7 | 17:51277125 | CATTTTGTACTTCTT[C/T]ATAGGTTGATGGGAA | 51096 |
rs753137909 | snp | C/T | | | missense, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51260682 | ACTGGAAAGCCGGAG[C/T]GGGGCCAGGCGGGCC | 51096 |
rs753156797 | in-del | -/AAA | 5.17389e-05 | 0.00508594 | cds-indel | UTP18 | GRCh38.p7 | 17:51266273 | CTTAAAAAGAGACTT[-/AAA]GAAGAGTAAGTGTCT | 51096 |
rs753230293 | snp | C/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51284454 | TTAATTATAAATTCC[C/T]GTGTTCTGGATCCGT | 51096 |
rs753311686 | snp | A/T | 1.72077e-05 | 0.00293318 | intron-variant | UTP18 | GRCh38.p7 | 17:51293889 | ACTTTAAAGTTTTTT[A/T]TTATCTCCTGCAGGT | 51096 |
rs753463505 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51286398 | AATGATTTCAGTCAA[A/G]TCCTCCCTGGGATGG | 51096 |
rs753477368 | snp | A/G | 1.9536e-05 | 0.00312532 | intron-variant | UTP18 | GRCh38.p7 | 17:51280116 | TGAAGGTAAAGCATT[A/G]TTATTGCTTCTTGTT | 51096 |
rs753488023 | snp | C/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51295162 | GTTGCCTGTTTACTC[C/T]GATGGTAGTTTCTTT | 51096 |
rs753494154 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51272712 | TAATTCTTTGATTTC[A/G]TCTTTAATCCTAGTG | 51096 |
rs753547204 | snp | A/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51274129 | TTCTGTTTCTTGGAC[A/T]TGCTGCTAGGTCCTT | 51096 |
rs753567959 | snp | C/T | 7.54916e-05 | 0.0061433 | intron-variant | UTP18 | GRCh38.p7 | 17:51263423 | CTGAATCCCTCTGTA[C/T]ACTTAAAAAAGTTAT | 51096 |
rs753620958 | in-del | -/CTT | | | intron-variant, utr-variant-3-prime | UTP18 | GRCh38.p7 | 17:51288838 | AAGTCCGGAGGAAAC[-/CTT]CTTCTAAGAGTCCTC | 51096 |
rs753645610 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51278496 | CGTTGGCCAAGATAC[A/G]GTTAGTGATCTTTAC | 51096 |
rs753691564 | in-del | -/CGCGGCGGCCGCTGCGATTGCAGT | 4.75636e-05 | 0.00487642 | cds-indel, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51260749 | GCCGGCCCGGCCGAG[-/CGCGGCGGCCGCTGCGATTGCAGT]CGCGGCGGCGGAGGA | 51096 |
rs753733021 | snp | A/G | 3.64604e-05 | 0.00426953 | missense, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51260611 | GCGGAGGAGACGAAT[A/G]AAACTGGACCGGAGA | 51096 |
rs753757690 | snp | C/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51267251 | TACAGAGGTGAGCCA[C/T]TGTGCTCAGCCATTA | 51096 |
rs753881675 | snp | C/T | 1.68012e-05 | 0.00289833 | intron-variant | UTP18 | GRCh38.p7 | 17:51297045 | CTGCAGGTTTTAAGA[C/T]ACACCCATTGCTGTC | 51096 |
rs753924069 | in-del | -/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51282867 | TTCTTCTTCTTCTTC[-/T]TTTTTTTTTTTTTTT | 51096 |
rs753927443 | snp | C/T | 1.66916e-05 | 0.00288886 | intron-variant | UTP18 | GRCh38.p7 | 17:51273357 | TCTGGGTTTGTTTGA[C/T]TTAGATGAAAGTGAA | 51096 |
rs754028411 | in-del | -/AGTA | | | intron-variant | UTP18 | GRCh38.p7 | 17:51265197 | TACTGCTTTTTTAAT[-/AGTA]AGTAGTTAACAGAGA | 51096 |
rs754065727 | snp | A/G | 1.66255e-05 | 0.00288314 | intron-variant | UTP18 | GRCh38.p7 | 17:51285206 | GCCTTTCAAGTTTAA[A/G]GCAAAATTAACAACT | 51096 |
rs754070570 | snp | G/T | 1.65614e-05 | 0.00287757 | missense | UTP18 | GRCh38.p7 | 17:51285325 | GGCAGTTTATATGGA[G/T]TAAGCATTGCCACAT | 51096 |
rs754125746 | in-del | -/A | 1.65608e-05 | 0.00287752 | frameshift-variant | UTP18 | GRCh38.p7 | 17:51285282 | GATGTGAACTCAAGG[-/A]AAGTGCCTTAACAGA | 51096 |
rs754213119 | snp | A/G | 7.51117e-05 | 0.00612782 | missense, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51260889 | GCGACGTCGAGAACG[A/G]CGAGGACGCGTTGCT | 51096 |
rs754246254 | snp | A/G | 0.000132972 | 0.00815281 | missense | UTP18 | GRCh38.p7 | 17:51277134 | CTTCTTTATAGGTTG[A/G]TGGGAAAACAAATCC | 51096 |
rs754272836 | snp | C/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51264160 | TCCTGCCTCAGCCTC[C/G]CGAGTAGCTGTGACT | 51096 |
rs754274102 | snp | A/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51295947 | GCCTTATGTTTAGAT[A/T]AGCTTTTGCTGATTT | 51096 |
rs754292240 | snp | A/C | 8.31234e-05 | 0.0064463 | synonymous-codon | UTP18 | GRCh38.p7 | 17:51293993 | ATGGATTTTTCTCCG[A/C]GAAGTGGATACTTTG | 51096 |
rs754323822 | snp | C/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51281962 | GGTGTGTTAAATTTT[C/G]TACATTATTGTCCTT | 51096 |
rs754340223 | snp | C/G | 4.76066e-05 | 0.00487863 | missense, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51260822 | CGGAACCGCCTGAGG[C/G]TGGAGGAGGACAAAC | 51096 |
rs754405359 | snp | A/G | 1.65641e-05 | 0.00287781 | missense | UTP18 | GRCh38.p7 | 17:51277267 | TTATGTCTATGACAT[A/G]CTGGCTGGAAAGTTA | 51096 |
rs754508986 | snp | C/T | 8.05899e-05 | 0.00634732 | missense, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51260901 | ACGACGAGGACGCGT[C/T]GCTGCGGCGTCTGCG | 51096 |
rs754520800 | snp | C/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51286427 | GGGAAGTCAAGGGGT[C/T]TTGTTGTCCAGAAAC | 51096 |
rs754573465 | snp | C/T | 3.32662e-05 | 0.00407824 | synonymous-codon | UTP18 | GRCh38.p7 | 17:51294010 | AAGTGGATACTTTGC[C/T]TTGGGGAATGAAAAG | 51096 |
rs754601097 | snp | C/T | | | intron-variant, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51262408 | ATTTGATAGTATAAA[C/T]TTTATGGTATAAATT | 51096 |
rs754613905 | snp | G/T | 6.62537e-05 | 0.00575521 | missense | UTP18 | GRCh38.p7 | 17:51277193 | TTTCCAATCTTTAAG[G/T]CTTGTTTTAGTGCTA | 51096 |
rs754740423 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51266781 | ATACCTAAGAAAATT[A/G]ACAGTTTACGGCTAG | 51096 |
rs754764117 | snp | A/G | 2.46472e-05 | 0.00351041 | utr-variant-5-prime, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51260540 | CCTGGGCGCATGCGC[A/G]GCGAGGTTCCACGTG | 51096 |
rs754774645 | snp | C/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51278603 | CCAGTATTTCTCCTT[C/T]TTCTGTTTTCACATT | 51096 |
rs755004332 | snp | C/G | | | missense | UTP18 | GRCh38.p7 | 17:51285311 | GATTTGTTGATGAAG[C/G]CAGTTTATATGGATT | 51096 |
rs755047344 | snp | A/G/T | 7.59076e-05 | 0.00616026 | intron-variant | UTP18 | GRCh38.p7 | 17:51280346 | TTGTGTGATTCTTCT[A/G/T]TATACTTTCTAACAG | 51096 |
rs755057497 | snp | G/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51269841 | ATCAAATAATGTATT[G/T]TGTGTGTGTGTGTGT | 51096 |
rs755062793 | snp | A/C | 1.68638e-05 | 0.00290373 | missense | UTP18 | GRCh38.p7 | 17:51280463 | TTCAGATAGTAAGAA[A/C]GTATACGCCTCTTCG | 51096 |
rs755132609 | snp | A/G | | | upstream-variant-2KB, intron-variant | UTP18, MBTD1 | GRCh38.p7 | 17:51258570 | GAAAGACTAGCTTCC[A/G]AGGAACACAGGTCAA | 51096 |
rs755276791 | snp | C/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51293481 | CACTAATTTGTAAAC[C/T]TTCTTAAAACATGAG | 51096 |
rs755297937 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51263482 | CCAATTTGTGATTAT[A/G]TGAAGATTTGAAAAA | 51096 |
rs755322303 | snp | C/G | 5.79805e-05 | 0.00538395 | synonymous-codon, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51260653 | GCCGAAGCGGAAGCC[C/G]GGAATGAGGCCGGAC | 51096 |
rs755327193 | snp | C/T | 1.745e-05 | 0.00295376 | intron-variant | UTP18 | GRCh38.p7 | 17:51275825 | AGAAAATAATGTTTA[C/T]TCATTTCAATTGATA | 51096 |
rs755331269 | snp | A/C | 1.69527e-05 | 0.00291137 | missense | UTP18 | GRCh38.p7 | 17:51288190 | CAGAAAAAATGAAAG[A/C]AGCAGTCAGATTGGT | 51096 |
rs755343904 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51292230 | AAGTAATTTCTCGAG[A/G]AACCTGTATAGAGAG | 51096 |
rs755366867 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51295967 | TTTGCTGATTTAATA[A/G]TTCAGTTTACTCCAC | 51096 |
rs755417129 | snp | A/G | 1.66018e-05 | 0.00288108 | missense | UTP18 | GRCh38.p7 | 17:51275902 | AATGCTGAACGTCCT[A/G]CTGTTGCTCGGATCT | 51096 |
rs755557323 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51282048 | TCTGACTTCCCTAAG[A/G]CTTGTTAACTCTTAC | 51096 |
rs755617734 | snp | C/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51267167 | TGAGGTTTTTCGCCA[C/T]GTCGCCCAGGCTGGT | 51096 |
rs755651922 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51294655 | AATAGTGCCGCATCA[A/G]TAAACATACATGTGC | 51096 |
rs755717432 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51285123 | TTCCAGAACTAGGAG[A/G]GTTATAATAGGTCTG | 51096 |
rs755719032 | snp | A/T | 1.88916e-05 | 0.00307335 | intron-variant | UTP18 | GRCh38.p7 | 17:51280001 | GCTTCATTTCCTATT[A/T]TAGGTTTGAAAGAGA | 51096 |
rs755725820 | snp | A/G | 1.65946e-05 | 0.00288046 | intron-variant | UTP18 | GRCh38.p7 | 17:51285389 | TAAAGAGAGGTTCTT[A/G]TAACCTTAATCACAT | 51096 |
rs755761031 | snp | C/T | 4.2252e-05 | 0.00459611 | missense, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51260906 | GAGGACGCGTTGCTG[C/T]GGCGTCTGCGAGGCC | 51096 |
rs755854197 | snp | A/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51271951 | GGAATTACAGATATG[A/T]GCCACCATGCCTGGC | 51096 |
rs755880185 | snp | G/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51276242 | TTCAATCACAGCTGC[G/T]CACCCCTTGCCTGTT | 51096 |
rs755903206 | snp | A/G | 1.68672e-05 | 0.00290402 | missense | UTP18 | GRCh38.p7 | 17:51294040 | GGGCAAGGCCCTGAT[A/G]TATAGGTAGGTATTA | 51096 |
rs755915644 | snp | C/T | 1.67382e-05 | 0.00289289 | intron-variant | UTP18 | GRCh38.p7 | 17:51297028 | CCCTTTTCTTACAAA[C/T]TCTGCAGGTTTTAAG | 51096 |
rs755933022 | snp | C/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51264758 | CGCGATCTTGGCTCA[C/G]TGCAACCTCCGCCTC | 51096 |
rs755935045 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51277111 | ATAATCAAAAGAACC[A/G]TTTTGTACTTCTTTA | 51096 |
rs756143737 | snp | C/G | 1.66482e-05 | 0.0028851 | intron-variant | UTP18 | GRCh38.p7 | 17:51285197 | AGTTTACTTGCCTTT[C/G]AAGTTTAAAGCAAAA | 51096 |
rs756153266 | snp | A/C | | | intron-variant | UTP18 | GRCh38.p7 | 17:51281889 | AGGTTTTCTGACTTT[A/C]TTTTTGAAAGTTACT | 51096 |
rs756154675 | snp | A/G | 1.90091e-05 | 0.00308288 | intron-variant | UTP18 | GRCh38.p7 | 17:51266318 | TTTACCAAGAGGTGT[A/G]TGTAACCAATGCCCA | 51096 |
rs756188949 | snp | C/T | | | utr-variant-3-prime | UTP18 | GRCh38.p7 | 17:51297869 | ATGGAAAATGATTTA[C/T]AGATCCAGCTGTGCT | 51096 |
rs756206141 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51280109 | CTAGCAATGAAGGTA[A/G]AGCATTATTATTGCT | 51096 |
rs756319201 | snp | C/T | 1.69697e-05 | 0.00291283 | missense | UTP18 | GRCh38.p7 | 17:51280474 | AGAAAGTATACGCCT[C/T]TTCGGGTAAGACAAC | 51096 |
rs756346440 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51269763 | GGTTGAAGGAATCTT[A/G]GTGATGTGGCCTGAC | 51096 |
rs756366029 | snp | A/G | 1.66785e-05 | 0.00288773 | intron-variant | UTP18 | GRCh38.p7 | 17:51277126 | ATTTTGTACTTCTTT[A/G]TAGGTTGATGGGAAA | 51096 |
rs756383980 | snp | C/G | | | intron-variant, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51261308 | TTTCGTTGATGGAAT[C/G]AATTCGTGGGCACGG | 51096 |
rs756467733 | snp | C/T | | | intron-variant, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51261623 | TTGGCGCTTGTGTGC[C/T]AGTGGCAGAGACAAG | 51096 |
rs756479587 | snp | C/G | 0.000250583 | 0.0111906 | missense, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51260749 | GCCGGCCCGGCCGAG[C/G]GCGGCGGCCGCTGCG | 51096 |
rs756567339 | snp | C/T | 5.45569e-05 | 0.00522259 | stop-gained, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51260804 | GAGAGACGGCTCCGG[C/T]AGCGGAACCGCCTGA | 51096 |
rs756590446 | in-del | -/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51270151 | TAATGTACTTTTTAC[-/T]AAACTGTTTTTTCCC | 51096 |
rs756624177 | in-del | -/G | 0.000439649 | 0.01482 | intron-variant | UTP18 | GRCh38.p7 | 17:51268799 | TTATGGACATGTAGT[-/G]GTTGCCATAAATATA | 51096 |
rs756629212 | snp | C/T | 1.66136e-05 | 0.00288211 | synonymous-codon | UTP18 | GRCh38.p7 | 17:51275937 | TGTGCAGTTCCATCC[C/T]GGTGCACAGATTGTG | 51096 |
rs756684482 | snp | A/G | 5.21789e-05 | 0.00510752 | missense | UTP18 | GRCh38.p7 | 17:51288058 | TGGTAAATATATACA[A/G]TCAAGATTCTTGTCT | 51096 |
rs756684856 | snp | C/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51293437 | ATCTTGTCCAACCCA[C/T]GGCGCAGGACGGTTT | 51096 |
rs756690339 | snp | C/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51264503 | TAAGGTTCTTGATAA[C/G]TACTGCCAGACTGCA | 51096 |
rs756812001 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51266505 | AATATAATCAGTGAT[A/G]ATATTGCTTACTTGT | 51096 |
rs756854108 | snp | C/G | 1.91057e-05 | 0.00309071 | intron-variant | UTP18 | GRCh38.p7 | 17:51263425 | GAATCCCTCTGTACA[C/G]TTAAAAAAGTTATTT | 51096 |
rs756854493 | in-del | -/ATT | | | intron-variant | UTP18 | GRCh38.p7 | 17:51264367 | TTCCCTTTAATGCAG[-/ATT]ATTTCAGCATTAATG | 51096 |
rs756977548 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51283777 | GTGCCACCACGCCCA[A/G]CTAATTTTTGTATTT | 51096 |
rs756991239 | snp | A/C | | | intron-variant | UTP18 | GRCh38.p7 | 17:51287883 | GGAGGTTCTATAGGA[A/C]ATCTGTGGCTATAGT | 51096 |
rs757075412 | snp | A/G | | | intron-variant, downstream-variant-500B | UTP18 | GRCh38.p7 | 17:51289494 | TTACAGGAGTGAGCC[A/G]CCGTGCCCAGCCCAG | 51096 |
rs757078044 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51274714 | GCCTCAGCTCCCAAC[A/G]TGCTGGGATTACAGG | 51096 |
rs757163415 | snp | C/G | 2.06371e-05 | 0.00321218 | intron-variant | UTP18 | GRCh38.p7 | 17:51280129 | TTATTATTGCTTCTT[C/G]TTCTTCTCCCACAAG | 51096 |
rs757193061 | in-del | -/GAA | | | intron-variant | UTP18 | GRCh38.p7 | 17:51291026 | CATGGAACTTTCTAC[-/GAA]CCATTAAATCAAGGA | 51096 |
rs757197347 | snp | C/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51276155 | CAGAGTTCATTTACT[C/T]GGAAATACAAAACAG | 51096 |
rs757257176 | snp | C/T | 3.33528e-05 | 0.00408354 | intron-variant | UTP18 | GRCh38.p7 | 17:51273358 | CTGGGTTTGTTTGAC[C/T]TAGATGAAAGTGAAG | 51096 |
rs757271915 | snp | C/G | 1.68332e-05 | 0.00290109 | intron-variant | UTP18 | GRCh38.p7 | 17:51297049 | AGGTTTTAAGATACA[C/G]CCATTGCTGTCAGTT | 51096 |
rs757323982 | snp | A/G | | | intron-variant, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51262023 | AGTAGAAACCACTTG[A/G]ACATTTCTATCATTG | 51096 |
rs757348078 | snp | A/C | 1.82061e-05 | 0.00301708 | missense, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51260615 | AGGAGACGAATGAAA[A/C]TGGACCGGAGAACCG | 51096 |
rs757354192 | in-del | -/TTGTCA | | | downstream-variant-500B | UTP18 | GRCh38.p7 | 17:51298297 | TATTACTTCAAATCT[-/TTGTCA]TTGTCATTGTCATTT | 51096 |
rs757365989 | snp | C/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51285483 | TAAACTATTCAGTAA[C/T]ATGAAATTGGTCAAC | 51096 |
rs757456737 | snp | A/G | 1.67335e-05 | 0.00289248 | intron-variant | UTP18 | GRCh38.p7 | 17:51268939 | TTTAAATTAGTACAT[A/G]AGTCCCTGTTCCTGT | 51096 |
rs757475822 | snp | A/G | 1.71237e-05 | 0.00292602 | intron-variant | UTP18 | GRCh38.p7 | 17:51294066 | TATTATTTATGTTTA[A/G]AAGTCAGAGATACCT | 51096 |
rs757487280 | snp | G/T | 1.65614e-05 | 0.00287757 | missense | UTP18 | GRCh38.p7 | 17:51285333 | ATATGGATTAAGCAT[G/T]GCCACATCTAGGAAT | 51096 |
rs757532364 | snp | A/C | | | intron-variant | UTP18 | GRCh38.p7 | 17:51282972 | CTCCCAAGTTCTAGC[A/C]ATTCTCCTGCCTCAG | 51096 |
rs757552271 | snp | A/C | | | intron-variant | UTP18 | GRCh38.p7 | 17:51284701 | TTTTTTTCCTGTAAA[A/C]CTAAAGGTACTGTCT | 51096 |
rs757592539 | snp | A/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51270859 | CAATTAGTCTGCTAC[A/T]GTATGGGATATGCTT | 51096 |
rs757605140 | snp | A/C | | | intron-variant | UTP18 | GRCh38.p7 | 17:51279824 | GTGCTTTGTAGTGAC[A/C]TTATGTTTGGGTCAA | 51096 |
rs757647420 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51271817 | GGATTACAGGTGTGC[A/G]CTACCATGCCTGGCT | 51096 |
rs757679753 | in-del | -/CGAAAAAA | 1.65811e-05 | 0.00287929 | intron-variant | UTP18 | GRCh38.p7 | 17:51285380 | TGGGTAAGTAAAGAG[-/CGAAAAAA]AGGTTCTTGTAACCT | 51096 |
rs757700390 | snp | C/T | | | intron-variant, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51261506 | CACATTTTGCTATCC[C/T]TTTAAATTCTATACC | 51096 |
rs757773802 | snp | A/G | 0.00018486 | 0.00961227 | missense, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51260825 | AACCGCCTGAGGCTG[A/G]AGGAGGACAAACCGG | 51096 |
rs757791298 | in-del | -/ATG | | | intron-variant | UTP18 | GRCh38.p7 | 17:51277600 | TGCAGCAGAAAAAGC[-/ATG]ATGAGCCATGGAGCT | 51096 |
rs757802057 | snp | C/G | 1.66407e-05 | 0.00288446 | missense | UTP18 | GRCh38.p7 | 17:51275950 | CCCGGTGCACAGATT[C/G]TGATGGTTGCTGGAT | 51096 |
rs757970093 | in-del | -/CTTTT | 1.7376e-05 | 0.00294749 | intron-variant | UTP18 | GRCh38.p7 | 17:51263400 | ATGTAAGTTGCCTAA[-/CTTTT]CTTCTGAATCCCTCT | 51096 |
rs757971997 | snp | A/T | 1.66192e-05 | 0.00288259 | missense | UTP18 | GRCh38.p7 | 17:51277135 | TTCTTTATAGGTTGA[A/T]GGGAAAACAAATCCT | 51096 |
rs758058530 | snp | G/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51288223 | ATATTTCATTACCCC[G/T]TTATTATTGTTATTT | 51096 |
rs758147719 | snp | C/G | 1.67646e-05 | 0.00289517 | missense | UTP18 | GRCh38.p7 | 17:51280432 | TTAATGGAAGGGTTG[C/G]AGCATCCACATTCTC | 51096 |
rs758239856 | snp | A/G | | | intron-variant, synonymous-codon | UTP18 | GRCh38.p7 | 17:51286525 | TATATCCCTACCACC[A/G]TTTGCAAATTGGAGT | 51096 |
rs758257316 | in-del | -/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51293127 | TTCCCTGTGATCAGA[-/T]TTTAGTATTCTTTAC | 51096 |
rs758272720 | in-del | -/C | | | intron-variant, downstream-variant-500B | UTP18 | GRCh38.p7 | 17:51289318 | CTTCTGCCTCAGTCT[-/C]CCTGAGTAGCTGGGA | 51096 |
rs758293766 | snp | A/G | 1.67733e-05 | 0.00289592 | synonymous-codon | UTP18 | GRCh38.p7 | 17:51266251 | AAGTAAACTTTCGAA[A/G]GACAACCTTAAAAAG | 51096 |
rs758312800 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51287666 | ACTGATTTGGATGTG[A/G]TGGGTGATAGGTGGT | 51096 |
rs758394742 | snp | A/C | 2.20675e-05 | 0.00332164 | intron-variant | UTP18 | GRCh38.p7 | 17:51280145 | TTCTTCTCCCACAAG[A/C]CACTAGTGTAGGGAT | 51096 |
rs758450696 | snp | C/G | 1.85651e-05 | 0.00304667 | missense, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51260639 | AGAACCGGAGCGAAG[C/G]CGAAGCGGAAGCCCG | 51096 |
rs758503780 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime | UTP18, MBTD1 | GRCh38.p7 | 17:51260142 | TCTCGCTTCCACCGT[A/G]GGACCCTCTGCAGGC | 51096 |
rs758609033 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51277509 | AACACTTACGGAATG[A/G]TCATAATTTGGAAAT | 51096 |
rs758634794 | snp | C/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51279909 | AATTTGAGCCACTTA[C/T]GTATTTTAAAAAGTA | 51096 |
rs758645398 | snp | C/T | 8.62924e-05 | 0.00656801 | intron-variant | UTP18 | GRCh38.p7 | 17:51273492 | CTATCTAACTACTTA[C/T]CTCTGCAGTTTAATT | 51096 |
rs758674660 | snp | C/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51297499 | GTGTCCTTTCAGGCC[C/T]GAGATGTGGTGGTTC | 51096 |
rs758696667 | in-del | -/TT | | | intron-variant | UTP18 | GRCh38.p7 | 17:51273081 | TTTCACTTCATCTTG[-/TT]TTAGTAACCATCTGT | 51096 |
rs758740907 | snp | C/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51291651 | GAGACAGAAGAATTG[C/G]TTGCCCCCAAGAGGC | 51096 |
rs758746523 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51282177 | TCTGCTCTGTGGGTA[A/G]TAGTCAGCAACCTCT | 51096 |
rs758762979 | snp | C/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51283700 | CTCACTACATCCTCT[C/G]CCTCCTGGGTTCAGG | 51096 |
rs758794147 | snp | A/G | 1.65647e-05 | 0.00287786 | synonymous-codon | UTP18 | GRCh38.p7 | 17:51285354 | ATCTAGGAATGGACA[A/G]TATGTTGCTTGTGGG | 51096 |
rs758795792 | snp | C/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51270170 | CTGTTTTTTCCCCTT[C/T]TTCCCTTTTCTTTAA | 51096 |
rs758857999 | snp | C/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51295764 | AGCTTGATGGGGATG[C/G]CATTGAATCTATAAA | 51096 |
rs759058180 | snp | G/T | | | intron-variant, utr-variant-3-prime | UTP18 | GRCh38.p7 | 17:51288911 | GAGTTGTAACAACAT[G/T]TGTTAAGTGTTTTCT | 51096 |
rs759069511 | snp | A/C | 0.00012666 | 0.007957 | intron-variant | UTP18 | GRCh38.p7 | 17:51279990 | TTTATTTAATTGCTT[A/C]ATTTCCTATTTTAGG | 51096 |
rs759092006 | in-del | -/TTG | 0.00102337 | 0.0225973 | intron-variant | UTP18 | GRCh38.p7 | 17:51297767 | GGTATGTAATTTCTT[-/TTG]TTCTTTCCTCAGGTC | 51096 |
rs759141647 | in-del | -/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51276807 | TATCTCCTTATCTGT[-/G]GGTGGACAAACTCAA | 51096 |
rs759145173 | snp | C/T | | | upstream-variant-2KB, intron-variant | UTP18, MBTD1 | GRCh38.p7 | 17:51259139 | CAGGGTTCAGACTAC[C/T]TACCACTTGTCAGAG | 51096 |
rs759193974 | snp | A/T | 3.31532e-05 | 0.0040713 | missense | UTP18 | GRCh38.p7 | 17:51273418 | GGGAATTTCATATCC[A/T]CATCAACTTCTCTTC | 51096 |
rs759197720 | snp | A/G | 1.65608e-05 | 0.00287752 | missense | UTP18 | GRCh38.p7 | 17:51285295 | AGGAAGTGCCTTAAC[A/G]GATTTGTTGATGAAG | 51096 |
rs759243690 | snp | A/G | 1.83316e-05 | 0.00302745 | synonymous-codon, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51260602 | GCCGCCGGAGCGGAG[A/G]AGACGAATGAAACTG | 51096 |
rs759259119 | snp | C/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51279592 | CAGCTAGTTTATATA[C/T]GTTTTTATGTTTTTG | 51096 |
rs759283533 | snp | A/C | 1.68838e-05 | 0.00290544 | intron-variant | UTP18 | GRCh38.p7 | 17:51273328 | GGCAGCTCATTGATT[A/C]TAAAGATCAGCCTTC | 51096 |
rs759319588 | snp | A/C | 1.83424e-05 | 0.00302834 | synonymous-codon, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51260629 | ACTGGACCGGAGAAC[A/C]GGAGCGAAGCCGAAG | 51096 |
rs759397316 | snp | C/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51292860 | GAGGTGAGCTTTTGG[C/G]TCTCTCTAAATCAGA | 51096 |
rs759518123 | snp | C/T | 1.82088e-05 | 0.00301729 | intron-variant | UTP18 | GRCh38.p7 | 17:51280521 | AGGATATTTTTACAT[C/T]TTAAATTTTAGGCCA | 51096 |
rs759599133 | snp | C/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51269395 | TATTTTCTGCTTCTT[C/T]GATCTTTTGAGTTTA | 51096 |
rs759670191 | snp | C/T | 1.66385e-05 | 0.00288426 | missense | UTP18 | GRCh38.p7 | 17:51293976 | TTTCTCATGTTCATA[C/T]CATGGATTTTTCTCC | 51096 |
rs759671595 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51284317 | AAATAGTGAGGATCC[A/G]CTTTTGAGATGGATG | 51096 |
rs759692114 | snp | C/T | 3.6529e-05 | 0.00427354 | synonymous-codon, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51260875 | GGAGCTGGTCTTCGG[C/T]GACGTCGAGAACGAC | 51096 |
rs759735049 | snp | C/T | 5.67295e-05 | 0.00532556 | missense, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51260795 | GCGGAGGAAGAGAGA[C/T]GGCTCCGGCAGCGGA | 51096 |
rs759895597 | snp | G/T | 4.62129e-05 | 0.00480669 | utr-variant-5-prime, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51260557 | CGAGGTTCCACGTGA[G/T]CGCCTGCGTTTCTCC | 51096 |
rs759910269 | snp | C/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51290095 | TGTGGTATATATATT[C/G]GGATTCTGCATATGA | 51096 |
rs759930759 | snp | A/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51283920 | ATGCCTGGCCATCTC[A/T]TGTTGCCTTTTTTGC | 51096 |
rs760004619 | snp | A/T | 1.72815e-05 | 0.00293946 | intron-variant | UTP18 | GRCh38.p7 | 17:51293878 | CCAGTTGTTACACTT[A/T]AAAGTTTTTTATTAT | 51096 |
rs760049909 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51265854 | GGCGTGAGCCACCAC[A/G]CTGGGCCTAAGGTTT | 51096 |
rs760083650 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51297416 | GTTTCACAGAGCTAG[A/G]TAATGGGGCTGGCCA | 51096 |
rs760198108 | snp | C/T | 3.63954e-05 | 0.00426572 | intron-variant | UTP18 | GRCh38.p7 | 17:51263415 | CTTTTCTTCTGAATC[C/T]CTCTGTACACTTAAA | 51096 |
rs760323549 | in-del | -/T | | | intron-variant, utr-variant-3-prime | UTP18 | GRCh38.p7 | 17:51289181 | CCACCCTTGTAAGCA[-/T]GACCTTTCTGTTTTT | 51096 |
rs760351468 | snp | A/G | 2.28511e-05 | 0.0033801 | missense, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51260678 | CCGGACTGGAAAGCC[A/G]GAGCGGGGCCAGGCG | 51096 |
rs760377380 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51272285 | TGTATTTTTAGTAGA[A/G]ACGGGGTTTCTCCAT | 51096 |
rs760403564 | in-del | -/CGG | | | upstream-variant-2KB, cds-indel | UTP18, MBTD1 | GRCh38.p7 | 17:51260502 | CGGCCCCCGGGGCTT[-/CGG]CGGCGGCGGCCCGCG | 51096 |
rs760404320 | snp | C/T | 3.31598e-05 | 0.00407171 | missense | UTP18 | GRCh38.p7 | 17:51273428 | TATCCACATCAACTT[C/T]TCTTCCAAGAGGAAT | 51096 |
rs760430209 | snp | C/T | | | intron-variant, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51261880 | AAGTGGCAGCAATCT[C/T]TTTGGGAAGTACAGA | 51096 |
rs760490086 | snp | C/T | 1.68179e-05 | 0.00289977 | intron-variant | UTP18 | GRCh38.p7 | 17:51275859 | TCCCAGCTTTCATTT[C/T]CTATAGATGAAGAAC | 51096 |
rs760537975 | snp | A/G | | | intron-variant, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51261248 | CCCAAACTGAGGGTG[A/G]TCTTTTGATCACCTG | 51096 |
rs760624310 | in-del | -/CA | 1.66145e-05 | 0.00288218 | frameshift-variant | UTP18 | GRCh38.p7 | 17:51275942 | AGTTCCATCCCGGTG[-/CA]CAGATTGTGATGGTT | 51096 |
rs760659164 | snp | G/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51263932 | ACATTTCTCCCTACT[G/T]AAAAAAAATAGACAT | 51096 |
rs760724191 | in-del | -/CCTGCGTTTCTCCTCAAA | 2.27311e-05 | 0.00337121 | utr-variant-5-prime, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51260559 | GGTTCCACGTGAGCG[-/CCTGCGTTTCTCCTCAAA]CCTGCGTTTCTCCTC | 51096 |
rs760766769 | in-del | -/A | | | utr-variant-3-prime | UTP18 | GRCh38.p7 | 17:51297918 | TAATAAACATGTGGC[-/A]GCTTTTGTTTGAAAA | 51096 |
rs760774596 | snp | C/T | 1.66977e-05 | 0.00288939 | intron-variant | UTP18 | GRCh38.p7 | 17:51277340 | ACACAACCAGTCATT[C/T]CCCCCAAGGTGAGTT | 51096 |
rs760790536 | snp | A/T | 1.65611e-05 | 0.00287755 | missense | UTP18 | GRCh38.p7 | 17:51285306 | TAACAGATTTGTTGA[A/T]GAAGGCAGTTTATAT | 51096 |
rs760792036 | snp | C/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51265041 | GACTTTTTAAATAAT[C/G]TTGGTATATTAGTTC | 51096 |
rs760812620 | snp | C/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51297170 | ACTGTCTAGCTGAAG[C/T]TGGACCCTCCTTTCT | 51096 |
rs760904790 | in-del | -/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51281677 | GTATCAGTGTCACTA[-/T]CCTGGTTGTAATGTT | 51096 |
rs760945069 | snp | C/G/T | 0.00022529 | 0.0106114 | missense, synonymous-codon, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51260887 | CGGCGACGTCGAGAA[C/G/T]GACGAGGACGCGTTG | 51096 |
rs761022696 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51275566 | GGGAAATGACTACAT[A/G]CTAGTGCTCCAAGAA | 51096 |
rs761031410 | snp | A/G | 2.07059e-05 | 0.00321753 | intron-variant, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51260949 | AGGCCGCGGCGCGCG[A/G]GCTGGGCGCACTCGG | 51096 |
rs761059679 | snp | C/T | 2.24545e-05 | 0.00335063 | utr-variant-5-prime, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51260560 | GGTTCCACGTGAGCG[C/T]CTGCGTTTCTCCTCA | 51096 |
rs761069636 | snp | A/G | 0.00010295 | 0.00717385 | intron-variant | UTP18 | GRCh38.p7 | 17:51293892 | TTAAAGTTTTTTATT[A/G]TCTCCTGCAGGTTCA | 51096 |
rs761118446 | snp | A/G | 1.65625e-05 | 0.00287766 | missense | UTP18 | GRCh38.p7 | 17:51277245 | CGAGTACCCACAGCA[A/G]GGTTCTTTATGTCTA | 51096 |
rs761124347 | snp | C/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51273878 | ATATTGCAGTAGCTT[C/T]GTGACTGGACTCTTT | 51096 |
rs761133457 | snp | A/T | | | intron-variant, missense | UTP18 | GRCh38.p7 | 17:51288575 | AACAGAACGGAGGCA[A/T]TTCTCGGGTTTTGAA | 51096 |
rs761177618 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51263196 | AACATTCTATGAGCC[A/G]TTTGGCTGTAAGGCC | 51096 |
rs761257805 | snp | A/G | 8.58421e-05 | 0.00655085 | intron-variant | UTP18 | GRCh38.p7 | 17:51268823 | AAATATATTTTTCAA[A/G]TATTTTTGCTTAGAT | 51096 |
rs761309686 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51291329 | AGGGAAGATTCACCA[A/G]TGCATTGAGAGATTA | 51096 |
rs761316312 | snp | G/T | 1.8731e-05 | 0.00306025 | synonymous-codon, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51260590 | AAACCTAACGATGCC[G/T]CCGGAGCGGAGGAGA | 51096 |
rs761324752 | snp | G/T | 1.66671e-05 | 0.00288674 | stop-gained | UTP18 | GRCh38.p7 | 17:51266234 | ATGAAAAATGCTAGT[G/T]AAAGTAAACTTTCGA | 51096 |
rs761348064 | snp | A/G | 1.74379e-05 | 0.00295273 | intron-variant | UTP18 | GRCh38.p7 | 17:51280499 | GACAACGACATGAAA[A/G]AAGCTAAGGATATTT | 51096 |
rs761368243 | in-del | -/C | 5.57243e-05 | 0.00527817 | frameshift-variant, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51260800 | GGAAGAGAGACGGCT[-/C]CGGCAGCGGAACCGC | 51096 |
rs761477825 | snp | A/C | | | intron-variant | UTP18 | GRCh38.p7 | 17:51275420 | TGTGCCAATTGAAGA[A/C]CTGTGGGGACAACTG | 51096 |
rs761480468 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51284148 | CTGCTTAACCTGCAC[A/G]CTTACTCTAGCCTGG | 51096 |
rs761507031 | snp | C/T | | | downstream-variant-500B | UTP18 | GRCh38.p7 | 17:51298285 | GCTTTTCTGGCCTTA[C/T]TACTTCAAATCTTTG | 51096 |
rs761552531 | snp | A/G | 1.69238e-05 | 0.00290888 | missense | UTP18 | GRCh38.p7 | 17:51280404 | ACCAAAGAACTGATT[A/G]GAAGCATGAAAATTA | 51096 |
rs761604394 | snp | C/T | 5.65435e-05 | 0.00531682 | missense, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51260778 | CGATTGCAGTCGCGG[C/T]GGCGGAGGAAGAGAG | 51096 |
rs761697514 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51270467 | ATTTTAGATTCCTGT[A/G]ATTTTGGGTATGGTT | 51096 |
rs761704482 | snp | A/G | 1.67108e-05 | 0.00289052 | missense | UTP18 | GRCh38.p7 | 17:51275869 | CATTTCCTATAGATG[A/G]AGAACTGCCAGCATG | 51096 |
rs761717183 | in-del | -/T | 1.66136e-05 | 0.00288211 | intron-variant | UTP18 | GRCh38.p7 | 17:51277311 | AAGTGAGAGGTAAGA[-/T]TTCTGTTGAATGCAC | 51096 |
rs761730091 | snp | A/G | 2.98254e-05 | 0.00386158 | intron-variant | UTP18 | GRCh38.p7 | 17:51287981 | ACTTAGGTTGTGAAA[A/G]CCCTTTTACTTGGTT | 51096 |
rs761750775 | snp | C/T | | | upstream-variant-2KB, intron-variant | UTP18, MBTD1 | GRCh38.p7 | 17:51259734 | GGATGGAGAAGCAGG[C/T]CAGGGAGCGGGGTCA | 51096 |
rs761788143 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51290485 | ACAGCATAGCATTTT[A/G]TTGCTATGCTGTTGA | 51096 |
rs761793357 | snp | C/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51273612 | TGTTTTTTTTTTTTC[C/G]TTTTGCAAAAAATGT | 51096 |
rs761800461 | snp | A/C | 3.02567e-05 | 0.0038894 | missense, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51260705 | GGCGGGCCTCCCCAA[A/C]AGCCTGCCCCTTCAT | 51096 |
rs761803758 | snp | C/T | | | intron-variant, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51261125 | AAAGTGCCTGGAGGG[C/T]GGGGACCGCGTCTTT | 51096 |
rs761922239 | snp | C/G | 1.66563e-05 | 0.0028858 | missense | UTP18 | GRCh38.p7 | 17:51263370 | TGGGTGGATGAAGAA[C/G]ATGAAGATGAGGAAA | 51096 |
rs761927306 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51263063 | CTCCTTGACTGTTCC[A/G]TCTTGCCTCACCTGT | 51096 |
rs761952001 | in-del | -/G | | | intron-variant, utr-variant-3-prime | UTP18 | GRCh38.p7 | 17:51288645 | TAATTTAAATAGCTA[-/G]GGTAGTACCTTTGAA | 51096 |
rs761972825 | snp | A/G | 1.6631e-05 | 0.00288362 | missense | UTP18 | GRCh38.p7 | 17:51288150 | CTGACCTTCAATCCT[A/G]CTACAGAAATCTTGG | 51096 |
rs762111361 | snp | C/G | 2.87708e-05 | 0.0037927 | intron-variant | UTP18 | GRCh38.p7 | 17:51279964 | TAGTTTTATTGAAAA[C/G]TATATAAAACTTTAT | 51096 |
rs762243981 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51286190 | TTACTGAAAACATTG[A/G]TTATTACACTGGGGA | 51096 |
rs762259775 | in-del | -/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51278452 | GCATCTCCTTGTCTT[-/G]GCATCCTCTTGAGAG | 51096 |
rs762279839 | snp | C/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51290165 | TCAGACCTGTAATCC[C/T]GGCACTTTGGGAGGC | 51096 |
rs762305548 | snp | C/T | 3.32519e-05 | 0.00407736 | synonymous-codon | UTP18 | GRCh38.p7 | 17:51296977 | CAGGTTGCACCATTA[C/T]TCAGACTTCTAAAGA | 51096 |
rs762355938 | in-del | -/TCTT | | | intron-variant | UTP18 | GRCh38.p7 | 17:51293260 | ACTGACGCTTTTTTC[-/TCTT]TCTTCCTTTTCTGCT | 51096 |
rs762377585 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51290302 | GCGTCTGTAATCCCA[A/G]CTACTCAGGAGGCTG | 51096 |
rs762497747 | snp | C/G | 1.66252e-05 | 0.00288311 | missense | UTP18 | GRCh38.p7 | 17:51293994 | TGGATTTTTCTCCGA[C/G]AAGTGGATACTTTGC | 51096 |
rs762539165 | in-del | -/ATT | 0.000307917 | 0.0124042 | intron-variant | UTP18 | GRCh38.p7 | 17:51280113 | CAATGAAGGTAAAGC[-/ATT]ATTATTGCTTCTTGT | 51096 |
rs762560099 | snp | C/G | 1.84869e-05 | 0.00304024 | missense, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51260596 | AACGATGCCGCCGGA[C/G]CGGAGGAGACGAATG | 51096 |
rs762630674 | in-del | -/GTC | | | intron-variant | UTP18 | GRCh38.p7 | 17:51276215 | CTTGCTCCAAAGTCT[-/GTC]GTCACTGTTTTCAAT | 51096 |
rs762636224 | snp | G/T | 1.65608e-05 | 0.00287752 | missense | UTP18 | GRCh38.p7 | 17:51285286 | GTGAACTCAAGGAAG[G/T]GCCTTAACAGATTTG | 51096 |
rs762640930 | snp | A/C | | | upstream-variant-2KB, utr-variant-5-prime, intron-variant | UTP18, MBTD1 | GRCh38.p7 | 17:51259143 | GTTCAGACTACCTAC[A/C]ACTTGTCAGAGAGGC | 51096 |
rs762668011 | snp | C/G | 4.97781e-05 | 0.00498864 | missense | UTP18 | GRCh38.p7 | 17:51268862 | GCCATGGGAGGAGTA[C/G]CTGCCTGGGCAGAGA | 51096 |
rs762679928 | snp | A/G | 7.03482e-05 | 0.00593036 | intron-variant | UTP18 | GRCh38.p7 | 17:51280508 | ATGAAAGAAGCTAAG[A/G]ATATTTTTACATTTT | 51096 |
rs762731700 | snp | C/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51290953 | TAAGCTGTTGGACTA[C/G]TAGGAGACTCAGAAG | 51096 |
rs762880005 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51270332 | TGTTAAACATCCCTC[A/G]TTATTTTGACCATTT | 51096 |
rs762888616 | snp | C/T | 9.97788e-05 | 0.00706254 | missense | UTP18 | GRCh38.p7 | 17:51275885 | AGAACTGCCAGCATG[C/T]GAATGCTGAACGTCC | 51096 |
rs762927140 | snp | C/T | 5.12431e-05 | 0.00506151 | missense, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51260781 | TTGCAGTCGCGGCGG[C/T]GGAGGAAGAGAGACG | 51096 |
rs762977343 | snp | A/G | 7.43025e-05 | 0.00609473 | synonymous-codon, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51260725 | TGCCCCTTCATCCCA[A/G]CGGAAACCGCCGGCC | 51096 |
rs762985908 | snp | G/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51271692 | TATTATTTTTTGAGT[G/T]AGTCTTGCTCTGTCG | 51096 |
rs762996780 | snp | A/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51277705 | GTTTTAGTGTTAGTT[A/T]TAATAAAATTTTGAT | 51096 |
rs763040914 | snp | C/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51272350 | GTGATCCACTCACCT[C/T]GGCCTCGCAAAGTGC | 51096 |
rs763093099 | snp | C/T | 1.65784e-05 | 0.00287905 | missense | UTP18 | GRCh38.p7 | 17:51273425 | TCATATCCACATCAA[C/T]TTCTCTTCCAAGAGG | 51096 |
rs763124885 | snp | C/T | 1.70714e-05 | 0.00292154 | intron-variant | UTP18 | GRCh38.p7 | 17:51277082 | TATACTACCAGGATA[C/T]AGGGTCTGTGGAAAT | 51096 |
rs763165604 | snp | C/T | | | intron-variant, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51261994 | TTGAAGGCTATTAGA[C/T]TAGTAGTAGAGCAAG | 51096 |
rs763263845 | snp | A/G | 1.66774e-05 | 0.00288763 | missense | UTP18 | GRCh38.p7 | 17:51288165 | ACTACAGAAATCTTG[A/G]CAATTGCTTCAGAAA | 51096 |
rs763391981 | in-del | -/AGCTT | | | intron-variant | UTP18 | GRCh38.p7 | 17:51284677 | TCAACTCAAACCAAC[-/AGCTT]GTGATTTTTTTCCTG | 51096 |
rs763397246 | snp | C/G | | | intron-variant, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51262343 | CCCGCCTCGGCCTCC[C/G]AAAGTGCTGAGACTA | 51096 |
rs763410356 | snp | C/T | | | downstream-variant-500B | UTP18 | GRCh38.p7 | 17:51298391 | GAAATGTTCATTATG[C/T]CAACTTAAATGTTTA | 51096 |
rs763459135 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51267030 | ATGGGGTTTCACTAT[A/G]TTGCTCAGGCTGGTC | 51096 |
rs763486920 | snp | C/T | 1.83937e-05 | 0.00303257 | intron-variant | UTP18 | GRCh38.p7 | 17:51263418 | TTCTTCTGAATCCCT[C/T]TGTACACTTAAAAAA | 51096 |
rs763503756 | snp | C/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51284502 | CTCTTCCATCATCAT[C/T]AACATTTTGGTATCT | 51096 |
rs763509687 | snp | A/G | 3.46723e-05 | 0.00416352 | intron-variant | UTP18 | GRCh38.p7 | 17:51263398 | AAATGTAAGTTGCCT[A/G]ACTTTTCTTCTGAAT | 51096 |
rs763558614 | snp | C/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51290364 | GAGGTTGCAGTGAGC[C/T]AAGATCGTGCCTCTG | 51096 |
rs763577694 | snp | G/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51284859 | TGAGGTCAAGAGTTC[G/T]AGACCAGCCTGGCCA | 51096 |
rs763633457 | snp | C/G | 6.79452e-05 | 0.0058282 | synonymous-codon | UTP18 | GRCh38.p7 | 17:51280400 | TTAGACCAAAGAACT[C/G]ATTGGAAGCATGAAA | 51096 |
rs763700673 | snp | G/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51275146 | AGGTTGTGGTGAGTC[G/T]AGATTACGCCATTGC | 51096 |
rs763786750 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51276881 | GTGCCTTCTCAGGGC[A/G]CGCCACCTCCTCAGC | 51096 |
rs763817481 | in-del | -/ATTG | | | intron-variant | UTP18 | GRCh38.p7 | 17:51269838 | TATATCAAATAATGT[-/ATTG]TGTGTGTGTGTGTGT | 51096 |
rs763818132 | snp | G/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51297584 | CAGAGATTAATGAAT[G/T]TTGAGGGACTTTGAG | 51096 |
rs763826006 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51265465 | GCAGGGTTCCACCAC[A/G]TTGGCCAGGCTGGTC | 51096 |
rs763835464 | snp | C/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51291090 | TGTACACTTAACTGT[C/T]GTGATAGAAATGGTA | 51096 |
rs763846851 | snp | A/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51266333 | ATGTAACCAATGCCC[A/T]GTCATTAACCGTAAC | 51096 |
rs763931118 | in-del | -/CTC | 2.0867e-05 | 0.00323003 | cds-indel, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51260569 | TGAGCGCCTGCGTTT[-/CTC]CTCAAACCTAACGAT | 51096 |
rs763940148 | snp | A/G | 1.82443e-05 | 0.00302024 | missense, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51260609 | GAGCGGAGGAGACGA[A/G]TGAAACTGGACCGGA | 51096 |
rs763953756 | snp | C/T | 3.35531e-05 | 0.00409578 | intron-variant | UTP18 | GRCh38.p7 | 17:51297039 | CAAATTCTGCAGGTT[C/T]TAAGATACACCCATT | 51096 |
rs763994472 | snp | C/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51270443 | GCTGCATTTATAGAA[C/T]CCCACAACATTTTAG | 51096 |
rs764019952 | snp | C/T | 1.65853e-05 | 0.00287964 | missense | UTP18 | GRCh38.p7 | 17:51273434 | CATCAACTTCTCTTC[C/T]AAGAGGAATCTTGAA | 51096 |
rs764090964 | snp | A/G | | | intron-variant, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51261999 | GGCTATTAGACTAGT[A/G]GTAGAGCAAGTAGAA | 51096 |
rs764191253 | snp | A/G | | | intron-variant, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51261462 | TTCTGGCAATGGCAA[A/G]CCCTGCGTGATTGAT | 51096 |
rs764231563 | snp | C/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51284917 | AATACAAAAATTAAC[C/T]ACGCATGGTGGCACA | 51096 |
rs764303557 | in-del | -/A | | | intron-variant | UTP18 | GRCh38.p7 | 17:51269838 | TATATCAAATAATGT[-/A]TTGTGTGTGTGTGTG | 51096 |
rs764316613 | snp | G/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51267068 | CCTGGACTCAAGAAA[G/T]CCTCCCACCTCAGCC | 51096 |
rs764319424 | in-del | -/GAA | | | intron-variant | UTP18 | GRCh38.p7 | 17:51282464 | AAGAAAGAAGAAAAT[-/GAA]GAGAAAGAGGAAGGA | 51096 |
rs764356853 | in-del | -/ACAC | | | downstream-variant-500B | UTP18 | GRCh38.p7 | 17:51297965 | TTCCCTCCACCCCCA[-/ACAC]ACACACACACAAACT | 51096 |
rs764387373 | snp | A/G | 1.66305e-05 | 0.00288357 | intron-variant | UTP18 | GRCh38.p7 | 17:51263223 | GGCCTATGTGTCTGC[A/G]GTCATGGGATAGGAA | 51096 |
rs764609014 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51287535 | TGTGCAACCAGAGGA[A/G]TGGAATTGTCATTGA | 51096 |
rs764690295 | snp | C/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51270204 | CTGTTAGACAGTTTT[C/T]CCTATTTTGAAATGT | 51096 |
rs764693106 | snp | C/T | 1.66699e-05 | 0.00288698 | intron-variant | UTP18 | GRCh38.p7 | 17:51277127 | TTTTGTACTTCTTTA[C/T]AGGTTGATGGGAAAA | 51096 |
rs764711930 | snp | C/G | | | missense, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51260837 | CTGGAGGAGGACAAA[C/G]CGGCCGTGGAGCGGT | 51096 |
rs764721900 | snp | C/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51286032 | TAGAATAAGTAACTT[C/T]GGGTTTAAATCTTAA | 51096 |
rs764793948 | snp | A/C | 1.66211e-05 | 0.00288275 | missense | UTP18 | GRCh38.p7 | 17:51268843 | TTTGCTTAGATTCCA[A/C]CATGCCATGGGAGGA | 51096 |
rs764846155 | snp | A/C | 0.000455507 | 0.0150846 | utr-variant-5-prime, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51260564 | CCACGTGAGCGCCTG[A/C]GTTTCTCCTCAAACC | 51096 |
rs764917498 | snp | C/T | | | intron-variant, utr-variant-3-prime | UTP18 | GRCh38.p7 | 17:51288963 | CTCATTGCAGAAGGT[C/T]TTTATTGGGACTTCA | 51096 |
rs764938645 | in-del | -/TTGT | | | intron-variant | UTP18 | GRCh38.p7 | 17:51269839 | ATATCAAATAATGTA[-/TTGT]GTGTGTGTGTGTGTG | 51096 |
rs764968967 | snp | C/G | | | intron-variant, utr-variant-3-prime | UTP18 | GRCh38.p7 | 17:51289110 | TATCATTTAGGGAAA[C/G]TTTCATGCCAGTATA | 51096 |
rs764999554 | in-del | -/GGA | 1.67172e-05 | 0.00289108 | cds-indel, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51260824 | GAACCGCCTGAGGCT[-/GGA]GGAGGACAAACCGGC | 51096 |
rs765046566 | snp | C/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51279604 | ATATGTTTTTATGTT[C/T]TTGGCTGTCTCTAGT | 51096 |
rs765092412 | snp | C/T | 2.14867e-05 | 0.00327763 | intron-variant | UTP18 | GRCh38.p7 | 17:51280138 | CTTCTTGTTCTTCTC[C/T]CACAAGACACTAGTG | 51096 |
rs765125746 | snp | A/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51269653 | ATGCAGGGAGTCCAT[A/T]CAAAGAGCCAGTGTT | 51096 |
rs765176725 | snp | A/G | 3.19412e-05 | 0.0039962 | missense, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51260711 | CCTCCCCAAAAGCCT[A/G]CCCCTTCATCCCAGC | 51096 |
rs765180262 | snp | C/T | 1.68704e-05 | 0.00290429 | synonymous-codon | UTP18 | GRCh38.p7 | 17:51280409 | AGAACTGATTGGAAG[C/T]ATGAAAATTAATGGA | 51096 |
rs765210027 | snp | A/T | 3.32701e-05 | 0.00407847 | synonymous-codon | UTP18 | GRCh38.p7 | 17:51288152 | GACCTTCAATCCTAC[A/T]ACAGAAATCTTGGCA | 51096 |
rs765231500 | snp | C/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51284401 | TTTTTTTTTAATCAT[C/T]TAAATAACTTGGTAA | 51096 |
rs765250517 | snp | C/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51271612 | TAGACCACAAATTCT[C/T]TCTACAGCTAATTTT | 51096 |
rs765303641 | snp | A/G | 1.67063e-05 | 0.00289014 | missense | UTP18 | GRCh38.p7 | 17:51275870 | ATTTCCTATAGATGA[A/G]GAACTGCCAGCATGC | 51096 |
rs765322786 | snp | A/C | | | intron-variant | UTP18 | GRCh38.p7 | 17:51270634 | ATCTTCAGGTTGGTT[A/C]TTCCAGAGTTGCCTA | 51096 |
rs765335042 | snp | C/T | 1.68148e-05 | 0.0028995 | intron-variant | UTP18 | GRCh38.p7 | 17:51273459 | CTTGAAGGTGAGAGT[C/T]AGTGAAGTTGGGGGA | 51096 |
rs765364527 | snp | A/G | 1.8396e-05 | 0.00303277 | missense, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51260633 | GACCGGAGAACCGGA[A/G]CGAAGCCGAAGCGGA | 51096 |
rs765458854 | snp | C/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51267815 | CTTGCTTATATCCCT[C/T]CTCTGAGGGATCACA | 51096 |
rs765472408 | snp | A/G | 1.6596e-05 | 0.00288058 | intron-variant | UTP18 | GRCh38.p7 | 17:51263253 | AAATCTCAGTGCTTG[A/G]GGGTGTTTTGTCTGC | 51096 |
rs765526929 | snp | C/T | 2.84353e-05 | 0.00377053 | intron-variant | UTP18 | GRCh38.p7 | 17:51287997 | CCCTTTTACTTGGTT[C/T]TTAATCTATTTTAAT | 51096 |
rs765651666 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51264209 | ACCTGGCTAATTTTT[A/G]TATTTTTAGTAGAGA | 51096 |
rs765707155 | snp | C/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51265945 | TGTGTGCAGATAAGT[C/G]ATGATGAATTTTCTC | 51096 |
rs765741239 | snp | C/T | 2.22348e-05 | 0.0033342 | intron-variant | UTP18 | GRCh38.p7 | 17:51279987 | AACTTTATTTAATTG[C/T]TTCATTTCCTATTTT | 51096 |
rs765764079 | snp | A/C | | | intron-variant | UTP18 | GRCh38.p7 | 17:51284208 | GAGATTCACTGAATT[A/C]TCATTGGGAGAATAA | 51096 |
rs765817335 | in-del | -/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51278843 | CTTTCATAGTAAGGA[-/G]ACTAGTCATCAGCAG | 51096 |
rs765933828 | snp | C/T | 4.98766e-05 | 0.00499357 | missense | UTP18 | GRCh38.p7 | 17:51296979 | GGTTGCACCATTACT[C/T]AGACTTCTAAAGAGA | 51096 |
rs765933878 | snp | A/C | 1.65671e-05 | 0.00287807 | missense | UTP18 | GRCh38.p7 | 17:51277277 | GACATGCTGGCTGGA[A/C]AGTTAATTCCTGTGC | 51096 |
rs766083318 | in-del | -/AA | | | synonymous-codon | UTP18 | GRCh38.p7 | 17:51296988 | ATTACTCAGACTTCT[-/AA]AGAGACTATTTGAAG | 51096 |
rs766097850 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51286384 | CAATTGAGCCATGAA[A/G]TGATTTCAGTCAAAT | 51096 |
rs766144701 | snp | A/T | 1.68935e-05 | 0.00290628 | intron-variant | UTP18 | GRCh38.p7 | 17:51273321 | TAAAAGGGGCAGCTC[A/T]TTGATTCTAAAGATC | 51096 |
rs766145018 | snp | C/T | 2.07518e-05 | 0.0032211 | utr-variant-5-prime, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51260569 | TGAGCGCCTGCGTTT[C/T]TCCTCAAACCTAACG | 51096 |
rs766156262 | snp | C/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51291595 | CAAAAATTAGCTGGG[C/T]GTGGTAGCCCACACC | 51096 |
rs766175093 | snp | A/G | 8.81516e-05 | 0.00663837 | intron-variant | UTP18 | GRCh38.p7 | 17:51280509 | TGAAAGAAGCTAAGG[A/G]TATTTTTACATTTTA | 51096 |
rs766259943 | snp | A/C | 3.35132e-05 | 0.00409334 | missense | UTP18 | GRCh38.p7 | 17:51280438 | GAAGGGTTGCAGCAT[A/C]CACATTCTCTTCAGA | 51096 |
rs766328551 | snp | C/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51278482 | GAAAGCGCACCATGC[C/G]TTGGCCAAGATACAG | 51096 |
rs766434695 | snp | C/G | 3.89522e-05 | 0.004413 | missense, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51260727 | CCCCTTCATCCCAGC[C/G]GAAACCGCCGGCCCG | 51096 |
rs766442657 | snp | G/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51281913 | AGTTACTTAAAATCA[G/T]CAGCCCTTGTAGCAA | 51096 |
rs766589345 | in-del | -/ACTA | | | intron-variant | UTP18 | GRCh38.p7 | 17:51284724 | TACTGTCTATTAATG[-/ACTA]ACTGATGCAGTTTTC | 51096 |
rs766628854 | snp | A/G | 0.000182844 | 0.00955974 | synonymous-codon | UTP18 | GRCh38.p7 | 17:51275886 | GAACTGCCAGCATGC[A/G]AATGCTGAACGTCCT | 51096 |
rs766635231 | in-del | -/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51268007 | TTTTTTTGTTTTTTG[-/T]TTTTTTGTTTTTTTT | 51096 |
rs766802744 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51279166 | ATCTACTATGTAGAA[A/G]TGAATGGATAGTGAA | 51096 |
rs766820307 | snp | C/G | 4.26803e-05 | 0.00461934 | intron-variant | UTP18 | GRCh38.p7 | 17:51288025 | AATCCTTTTCTCTTT[C/G]TAGTTCTAATTGTGG | 51096 |
rs766887282 | snp | C/T | 3.51667e-05 | 0.0041931 | intron-variant | UTP18 | GRCh38.p7 | 17:51263403 | TAAGTTGCCTAACTT[C/T]TCTTCTGAATCCCTC | 51096 |
rs766908510 | snp | A/G | 1.68134e-05 | 0.00289938 | synonymous-codon | UTP18 | GRCh38.p7 | 17:51288182 | AATTGCTTCAGAAAA[A/G]ATGAAAGAAGCAGTC | 51096 |
rs766975063 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51263189 | TAGAAAAAACATTCT[A/G]TGAGCCATTTGGCTG | 51096 |
rs766975154 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51278258 | AGATTCTGATTCTGT[A/G]GGTCTTAGGTGGGTT | 51096 |
rs766980314 | snp | C/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51263996 | ATTAACCATAATTTA[C/T]GTGGCTATTGTTGGG | 51096 |
rs766991814 | snp | C/T | 1.9488e-05 | 0.00312148 | intron-variant | UTP18 | GRCh38.p7 | 17:51279997 | AATTGCTTCATTTCC[C/T]ATTTTAGGTTTGAAA | 51096 |
rs767076120 | in-del | -/A | | | frameshift-variant | UTP18 | GRCh38.p7 | 17:51277207 | GCTTGTTTTAGTGCT[-/A]AATGGGGAAGAAGTT | 51096 |
rs767111503 | snp | C/G | 5.01015e-05 | 0.00500482 | intron-variant | UTP18 | GRCh38.p7 | 17:51297014 | TTGAAGTAAGAAAAC[C/G]CTTTTCTTACAAATT | 51096 |
rs767125337 | snp | C/T | 1.81289e-05 | 0.00301067 | synonymous-codon | UTP18 | GRCh38.p7 | 17:51280094 | GGATATTTGCATTTG[C/T]TAGCAATGAAGGTAA | 51096 |
rs767141667 | snp | C/T | 1.66333e-05 | 0.00288381 | synonymous-codon | UTP18 | GRCh38.p7 | 17:51294011 | AGTGGATACTTTGCC[C/T]TGGGGAATGAAAAGG | 51096 |
rs767215275 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51284899 | AACCCTGTCTCTACT[A/G]AAAATACAAAAATTA | 51096 |
rs767257031 | in-del | -/TC | | | intron-variant | UTP18 | GRCh38.p7 | 17:51267961 | AAAAATTAAAACAAC[-/TC]TCTTTGCCCTCTTCC | 51096 |
rs767295251 | snp | A/G | 1.68593e-05 | 0.00290334 | intron-variant | UTP18 | GRCh38.p7 | 17:51273332 | GCTCATTGATTCTAA[A/G]GATCAGCCTTCTGGG | 51096 |
rs767362999 | snp | A/G | 1.66438e-05 | 0.00288472 | intron-variant | UTP18 | GRCh38.p7 | 17:51268909 | ATCTTCAGATGGTGA[A/G]CGTTGATATTTCTGT | 51096 |
rs767372522 | snp | C/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51271320 | TTTTGGTTTGGTTTT[C/T]TTTTGAGACAGGGTC | 51096 |
rs767425346 | snp | C/G/T | | | intron-variant, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51261163 | CCTGGAGGCGCCGCT[C/G/T]CTCGGGTATCTGCTT | 51096 |
rs767449551 | snp | C/T | 3.31219e-05 | 0.00406938 | synonymous-codon | UTP18 | GRCh38.p7 | 17:51285300 | GTGCCTTAACAGATT[C/T]GTTGATGAAGGCAGT | 51096 |
rs767492193 | snp | C/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51276965 | TTTTATGAAGGCCTC[C/T]TGACATAGGCATGGT | 51096 |
rs767500503 | snp | C/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51291348 | ATTGAGAGATTACAC[C/T]GGGGAATTTTGCAGG | 51096 |
rs767537559 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51263157 | GCATTCCATCCCATT[A/G]TTTCATCAGAGAGTG | 51096 |
rs767589327 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51293328 | TGTGTACACATGGAC[A/G]CAGTAGAATAATAGG | 51096 |
rs767654333 | snp | A/T | 3.67505e-05 | 0.00428648 | missense, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51260880 | TGGTCTTCGGCGACG[A/T]CGAGAACGACGAGGA | 51096 |
rs767790765 | in-del | -/GGTGGGTGG | | | intron-variant | UTP18 | GRCh38.p7 | 17:51290184 | ACTTTGGGAGGCTGA[-/GGTGGGTGG]ATCACTTGAGGTCAG | 51096 |
rs767855432 | snp | A/G | 5.6365e-05 | 0.00530842 | missense, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51260796 | CGGAGGAAGAGAGAC[A/G]GCTCCGGCAGCGGAA | 51096 |
rs767897082 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51272573 | AGATTAATTAGATCT[A/G]GGATGATGGTTTATA | 51096 |
rs767997396 | in-del | -/TGTTTTTTT | | | intron-variant | UTP18 | GRCh38.p7 | 17:51289190 | GTAAGCAGACCTTTC[-/TGTTTTTTT]TGTTTTTTTTTTTTT | 51096 |
rs768005234 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51277707 | TTTAGTGTTAGTTAT[A/G]ATAAAATTTTGATTT | 51096 |
rs768049603 | snp | C/G | 3.35655e-05 | 0.00409654 | intron-variant | UTP18 | GRCh38.p7 | 17:51277116 | CAAAAGAACCATTTT[C/G]TACTTCTTTATAGGT | 51096 |
rs768070328 | snp | C/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51264923 | GTTGACCTCAAGTGA[C/G]CTGTTTGCCTCGGCC | 51096 |
rs768267240 | snp | A/T | | | downstream-variant-500B | UTP18 | GRCh38.p7 | 17:51298012 | GACTAAACATGAGAA[A/T]TTGGAAACACCTGTC | 51096 |
rs768285503 | snp | A/G | 0.000185753 | 0.00963545 | intron-variant, utr-variant-3-prime | UTP18 | GRCh38.p7 | 17:51288607 | GTAAGTTGAACTTGA[A/G]AATTAAATTGTATAA | 51096 |
rs768365504 | snp | C/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51292002 | CCTGATGCTTTGGAT[C/T]ATCTGTTCATAGTTG | 51096 |
rs768371518 | snp | G/T | 2.30195e-05 | 0.00339252 | missense, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51260679 | CGGACTGGAAAGCCG[G/T]AGCGGGGCCAGGCGG | 51096 |
rs768388026 | snp | A/G | 1.67784e-05 | 0.00289636 | intron-variant | UTP18 | GRCh38.p7 | 17:51275862 | CAGCTTTCATTTCCT[A/G]TAGATGAAGAACTGC | 51096 |
rs768478006 | snp | C/T | 1.83454e-05 | 0.00302859 | intron-variant | UTP18 | GRCh38.p7 | 17:51276002 | TTCAGGTATGCATCT[C/T]TATTTACTTATTTAT | 51096 |
rs768581767 | snp | C/T | 0.000132542 | 0.00813964 | missense | UTP18 | GRCh38.p7 | 17:51263337 | AAAGGTAATTTTCCA[C/T]CTCAAAAGAAGCCAG | 51096 |
rs768587226 | snp | C/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51281133 | ACTGAGCTGAGATCA[C/T]GTCTCAAAATATATA | 51096 |
rs768692888 | in-del | -/TAAAGTTTTTTATTATCTCC | 0.000120989 | 0.00777688 | intron-variant | UTP18 | GRCh38.p7 | 17:51293877 | CCAGTTGTTACACTT[-/TAAAGTTTTTTATTATCTCC]TAAAGTTTTTTATTA | 51096 |
rs768782538 | in-del | -/TTATTTATTTCTAATGCATTATTT | 7.40569e-05 | 0.00608465 | intron-variant | UTP18 | GRCh38.p7 | 17:51276010 | TGCATCTTTATTTAC[-/TTATTTATTTCTAATGCATTATTT]TTATTTAAGGACCAG | 51096 |
rs768834866 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51272815 | TCCCTTCTTAGCTCC[A/G]CAAGTGTTTTAAGTT | 51096 |
rs768884414 | in-del | -/TATATTTT | | | intron-variant | UTP18 | GRCh38.p7 | 17:51271574 | GTACTTCAGTCTGGG[-/TATATTTT]TATATTTTTCTGATT | 51096 |
rs768972116 | snp | C/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51290143 | TTGTTGCGCTGGGCA[C/T]GGTGGCTCAGACCTG | 51096 |
rs768985330 | snp | C/T | 8.31193e-05 | 0.00644614 | missense | UTP18 | GRCh38.p7 | 17:51296972 | TTTTCCAGGTTGCAC[C/T]ATTACTCAGACTTCT | 51096 |
rs769014915 | snp | C/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51279333 | AGTCCCCTGTATAGT[C/G]AATATGAACCTTTCA | 51096 |
rs769033713 | snp | C/T | 1.86322e-05 | 0.00305217 | missense, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51260592 | ACCTAACGATGCCGC[C/T]GGAGCGGAGGAGACG | 51096 |
rs769101241 | snp | C/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51268978 | ATTTGAGCTTTCTTA[C/T]GAGGCTCATTAAAAC | 51096 |
rs769128977 | snp | C/T | 1.6696e-05 | 0.00288924 | intron-variant | UTP18 | GRCh38.p7 | 17:51277341 | CACAACCAGTCATTC[C/T]CCCCAAGGTGAGTTT | 51096 |
rs769180428 | in-del | -/GAA | | | intron-variant | UTP18 | GRCh38.p7 | 17:51275415 | CAACCTGTGCCAATT[-/GAA]GAACTGTGGGGACAA | 51096 |
rs769373201 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51283905 | CAGGCATGAGCCACC[A/G]TGCCTGGCCATCTCA | 51096 |
rs769381524 | snp | C/G | 1.65608e-05 | 0.00287752 | missense | UTP18 | GRCh38.p7 | 17:51285276 | TGTTTGGGATGTGAA[C/G]TCAAGGAAGTGCCTT | 51096 |
rs769454269 | in-del | -/CT | | | intron-variant, downstream-variant-500B | UTP18 | GRCh38.p7 | 17:51289546 | TTGGGCCTATGTAAA[-/CT]CTTTTCTGCCCAACA | 51096 |
rs769454687 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51280272 | AGCTTTTGATTACAG[A/G]GAAAAATAAAGTTGA | 51096 |
rs769471546 | snp | C/T | 1.70081e-05 | 0.00291612 | intron-variant | UTP18 | GRCh38.p7 | 17:51268956 | GTCCCTGTTCCTGTT[C/T]GTTATTATTTGAGCT | 51096 |
rs769493118 | snp | C/T | | | intron-variant, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51262291 | GGGTTTCACCATCTT[C/T]GCCAGGCTGGTCTCA | 51096 |
rs769541287 | snp | A/G/T | 5.65084e-05 | 0.00531517 | missense, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51260780 | ATTGCAGTCGCGGCG[A/G/T]CGGAGGAAGAGAGAC | 51096 |
rs769552857 | snp | C/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51263804 | GCACAGTGCCTGAAA[C/T]TGAGTAAAGGCTAAA | 51096 |
rs769572381 | snp | A/G | 1.75293e-05 | 0.00296046 | intron-variant | UTP18 | GRCh38.p7 | 17:51280505 | GACATGAAAGAAGCT[A/G]AGGATATTTTTACAT | 51096 |
rs769586832 | in-del | -/CAAAGTTGTT | 3.34308e-05 | 0.00408831 | intron-variant | UTP18 | GRCh38.p7 | 17:51296927 | CACTGTGGGTAATTA[-/CAAAGTTGTT]CAAAGTTGTTCAGAT | 51096 |
rs769633038 | snp | C/T | 1.67133e-05 | 0.00289074 | synonymous-codon | UTP18 | GRCh38.p7 | 17:51293938 | AGTATTTTCAAACTT[C/T]CCAGTCATTAAAAAT | 51096 |
rs769768681 | in-del | -/AGGA | | | intron-variant | UTP18 | GRCh38.p7 | 17:51282474 | AAAATGAAGAGAAAG[-/AGGA]AGGAAGGGAGGGAGG | 51096 |
rs769771406 | in-del | -/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51283174 | GCGCCCAGCCACTTC[-/T]TTTTTTTTTTTTCAG | 51096 |
rs769788087 | snp | G/T | 1.92239e-05 | 0.00310026 | intron-variant | UTP18 | GRCh38.p7 | 17:51276021 | TTACTTATTTATTTC[G/T]AATGCATTATTTTTA | 51096 |
rs769836728 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51296887 | CTAAAATCTTCCTAA[A/G]TGCCCTTCTGTGATC | 51096 |
rs769881267 | snp | C/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51285855 | GGAACATACGCCCTG[C/T]CAGATAAGAAGGGAT | 51096 |
rs769895077 | snp | C/T | 5.14787e-05 | 0.00507314 | intron-variant | UTP18 | GRCh38.p7 | 17:51266173 | AAATATGCTGTTCTG[C/T]TTTTGTAGGGTTGAC | 51096 |
rs769920848 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51282528 | GAAGGAAGGAAGGAA[A/G]GAAAGAAAGAAAGAA | 51096 |
rs769921515 | snp | G/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51297253 | GTTGCATTCAATAAT[G/T]CTCATCAAAATTGTA | 51096 |
rs769939760 | snp | C/G | 2.43276e-05 | 0.00348758 | utr-variant-5-prime, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51260546 | CGCATGCGCAGCGAG[C/G]TTCCACGTGAGCGCC | 51096 |
rs769984355 | snp | C/T | 7.23079e-05 | 0.00601238 | intron-variant | UTP18 | GRCh38.p7 | 17:51293860 | TTTAAGAAACATGAG[C/T]TCCCAGTTGTTACAC | 51096 |
rs770073277 | snp | A/G | | | intron-variant, missense | UTP18 | GRCh38.p7 | 17:51286587 | GGAGCTTGGAGACCA[A/G]GCCATCTGCCTTAGG | 51096 |
rs770103950 | in-del | -/T | | | intron-variant, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51262092 | TGGTCTAGGTTTAGA[-/T]TTTTTTTTTTTTTTA | 51096 |
rs770131768 | snp | C/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51291220 | TTTATAGGCATTTTT[C/T]CTAATTAATAGTTCA | 51096 |
rs770234602 | in-del | -/C | | | intron-variant | UTP18 | GRCh38.p7 | 17:51287602 | ATAATATGCATGTGG[-/C]CACCCCCACAAACCT | 51096 |
rs770238004 | snp | A/G | 1.67058e-05 | 0.00289009 | missense | UTP18 | GRCh38.p7 | 17:51263376 | GATGAAGAAGATGAA[A/G]ATGAGGAAATGTAAG | 51096 |
rs770240450 | snp | A/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51276768 | ACTTGGTCCAGTTCA[A/T]GTAGTTTGGATGGGA | 51096 |
rs770293670 | snp | C/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51277998 | GCTCTCCCTATTAAA[C/T]TGTACATGCATGTGG | 51096 |
rs770315404 | snp | C/T | | | intron-variant, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51262050 | ATTGGTTTTGGGAAG[C/T]TCAAACTCACTTCAA | 51096 |
rs770374516 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51282297 | TATTTTTTAACTTTT[A/G]AAAAGGATTAATTTT | 51096 |
rs770398908 | snp | G/T | 1.72436e-05 | 0.00293624 | intron-variant | UTP18 | GRCh38.p7 | 17:51275837 | TTATTCATTTCAATT[G/T]ATAAAATCCCAGCTT | 51096 |
rs770420550 | snp | C/T | 2.01225e-05 | 0.00317189 | missense, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51260663 | AAGCCCGGAATGAGG[C/T]CGGACTGGAAAGCCG | 51096 |
rs770437048 | snp | C/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51269526 | GTATATCCTCTCACA[C/T]CATGTGGGAGCTCCT | 51096 |
rs770486136 | in-del | -/CGGGGCTTCGGCGGCGGCGGCCCG | | | upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51260494 | GCTCCTTCCGGCCCC[-/CGGGGCTTCGGCGGCGGCGGCCCG]CGAGGGGCCTGGGCG | 51096 |
rs770487902 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51279110 | TTTAAAAATATAGAC[A/G]TATATTTTTGACTAG | 51096 |
rs770526806 | snp | C/G | 1.65778e-05 | 0.002879 | missense | UTP18 | GRCh38.p7 | 17:51273401 | ATTTGTTGCAAAGGA[C/G]TGGGAATTTCATATC | 51096 |
rs770591171 | snp | C/G | 4.79122e-05 | 0.00489426 | missense, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51260915 | TTGCTGCGGCGTCTG[C/G]GAGGCCCGAGGGTGA | 51096 |
rs770614722 | snp | A/G | 1.83102e-05 | 0.00302568 | missense, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51260625 | TGAAACTGGACCGGA[A/G]AACCGGAGCGAAGCC | 51096 |
rs770617553 | in-del | -/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51282617 | GGGAGGGAGAAGAGG[-/T]TGGGGAGGGAAAAGA | 51096 |
rs770633454 | snp | C/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51270213 | AGTTTTTCCTATTTT[C/G]AAATGTATGTCCCAA | 51096 |
rs770701694 | snp | A/G/T | 3.3122e-05 | 0.00406941 | synonymous-codon | UTP18 | GRCh38.p7 | 17:51285291 | CTCAAGGAAGTGCCT[A/G/T]AACAGATTTGTTGAT | 51096 |
rs770763378 | in-del | -/TG | | | intron-variant | UTP18 | GRCh38.p7 | 17:51287769 | GGAGAAAGAGGTGAC[-/TG]TGAAGGAATCAGGAT | 51096 |
rs770888234 | snp | C/T | 0.000362924 | 0.0134659 | synonymous-codon, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51260869 | CTTGGAGGAGCTGGT[C/T]TTCGGCGACGTCGAG | 51096 |
rs770955552 | snp | C/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51263697 | TGGGCAGTTTGGAAC[C/G]TACATTTTTTCCTTT | 51096 |
rs770965608 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51293835 | CAGGAAGATAGAGTG[A/G]AGATTACAATTTAAG | 51096 |
rs771003186 | snp | C/T | 1.66266e-05 | 0.00288323 | intron-variant | UTP18 | GRCh38.p7 | 17:51277317 | GAGGTAAGATTTCTG[C/T]TGAATGCACACAACC | 51096 |
rs771040952 | in-del | -/G | 1.68233e-05 | 0.00290023 | intron-variant | UTP18 | GRCh38.p7 | 17:51273461 | TGAAGGTGAGAGTCA[-/G]TGAAGTTGGGGGATC | 51096 |
rs771077981 | snp | C/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51266873 | TAAATTTATATATTT[C/T]TTTGAGGTAGGATCT | 51096 |
rs771088771 | snp | C/T | 1.66499e-05 | 0.00288525 | missense | UTP18 | GRCh38.p7 | 17:51293966 | AATAAGAATATTTCT[C/T]ATGTTCATACCATGG | 51096 |
rs771119762 | snp | A/G | | | downstream-variant-500B | UTP18 | GRCh38.p7 | 17:51298141 | ATCCTCCATGCTTTA[A/G]GGGATCAGCTAACAG | 51096 |
rs771128021 | snp | A/C | 4.76894e-05 | 0.00488287 | utr-variant-5-prime, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51260551 | GCGCAGCGAGGTTCC[A/C]CGTGAGCGCCTGCGT | 51096 |
rs771176826 | snp | A/T | 3.31241e-05 | 0.00406952 | missense | UTP18 | GRCh38.p7 | 17:51277218 | GTGCTAATGGGGAAG[A/T]AGTTTTAGCCACGAG | 51096 |
rs771249702 | snp | A/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51284225 | CATTGGGAGAATAAG[A/T]GTACATATGGAAGGG | 51096 |
rs771261001 | snp | A/G | | | upstream-variant-2KB, intron-variant | UTP18, MBTD1 | GRCh38.p7 | 17:51258982 | TGTGAGAGAAAATTT[A/G]AGAAGTAAAAAAAGG | 51096 |
rs771287169 | snp | A/T | 5.19674e-05 | 0.00509716 | intron-variant | UTP18 | GRCh38.p7 | 17:51293872 | GAGCTCCCAGTTGTT[A/T]CACTTTAAAGTTTTT | 51096 |
rs771322533 | snp | C/G | 1.84286e-05 | 0.00303545 | intron-variant | UTP18 | GRCh38.p7 | 17:51268791 | ATCAAGCTTTATGGA[C/G]ATGTAGTGGTTGCCA | 51096 |
rs771343553 | snp | A/T | 1.71097e-05 | 0.00292481 | missense | UTP18 | GRCh38.p7 | 17:51280393 | TATTGTTTTAGACCA[A/T]AGAACTGATTGGAAG | 51096 |
rs771527473 | snp | A/G | 5.09671e-05 | 0.00504787 | missense, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51260756 | CGGCCGAGCGCGGCG[A/G]CCGCTGCGATTGCAG | 51096 |
rs771568721 | snp | A/G | 2.20393e-05 | 0.00331951 | synonymous-codon, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51260674 | GAGGCCGGACTGGAA[A/G]GCCGGAGCGGGGCCA | 51096 |
rs771636425 | snp | C/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51276527 | GCGATAATATAACCT[C/T]ATGACTTTACTGGGT | 51096 |
rs771704842 | snp | G/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51285540 | TCTTTGTGCAGTGTT[G/T]AATAATAATATTACA | 51096 |
rs771768895 | snp | C/T | 1.70458e-05 | 0.00291935 | intron-variant | UTP18 | GRCh38.p7 | 17:51275846 | TCAATTGATAAAATC[C/T]CAGCTTTCATTTCCT | 51096 |
rs771827580 | snp | C/T | 3.31526e-05 | 0.00407127 | missense | UTP18 | GRCh38.p7 | 17:51273419 | GGAATTTCATATCCA[C/T]ATCAACTTCTCTTCC | 51096 |
rs771887044 | in-del | -/AC | | | downstream-variant-500B | UTP18 | GRCh38.p7 | 17:51297967 | CCCTCCACCCCCAAC[-/AC]ACACACACACAAACT | 51096 |
rs771917115 | snp | A/G | 1.68295e-05 | 0.00290077 | missense | UTP18 | GRCh38.p7 | 17:51288081 | TCTTGTCTCCAAGAA[A/G]CAAACCCAAAGCCAA | 51096 |
rs771997459 | snp | A/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51275473 | CCATGAATGCAAAGA[A/T]GCCAGGTGCCAAAGT | 51096 |
rs772117190 | snp | A/G | 1.65666e-05 | 0.00287802 | missense | UTP18 | GRCh38.p7 | 17:51263326 | AGAATGAAGCAAAAG[A/G]TAATTTTCCACCTCA | 51096 |
rs772145981 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51263919 | AGTTACTTTGTAAAC[A/G]TTTCTCCCTACTTAA | 51096 |
rs772149350 | in-del | -/A | 1.66043e-05 | 0.00288129 | frameshift-variant | UTP18 | GRCh38.p7 | 17:51275927 | GGATCTCATCTGTGC[-/A]GTTCCATCCCGGTGC | 51096 |
rs772185300 | snp | G/T | 1.67016e-05 | 0.00288973 | intron-variant | UTP18 | GRCh38.p7 | 17:51296936 | GTAATTACAAAGTTG[G/T]TCAGATGACTTATTT | 51096 |
rs772196868 | snp | A/G | | | intron-variant, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51261838 | TGTCAGCTGCTTACC[A/G]GAGCCGCCTTCGGGT | 51096 |
rs772229486 | snp | C/T | 3.33117e-05 | 0.00408102 | intron-variant | UTP18 | GRCh38.p7 | 17:51277331 | GTTGAATGCACACAA[C/T]CAGTCATTCCCCCCA | 51096 |
rs772398470 | snp | G/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51297095 | TTAGCTGAGCTTTGT[G/T]TCTCTACCCCTAAGT | 51096 |
rs772426723 | snp | A/C | 1.65622e-05 | 0.00287764 | synonymous-codon | UTP18 | GRCh38.p7 | 17:51277237 | TTTAGCCACGAGTAC[A/C]CACAGCAAGGTTCTT | 51096 |
rs772439408 | snp | C/T | 1.68397e-05 | 0.00290165 | intron-variant | UTP18 | GRCh38.p7 | 17:51268948 | GTACATAAGTCCCTG[C/T]TCCTGTTCGTTATTA | 51096 |
rs772467032 | snp | G/T | 3.66643e-05 | 0.00428145 | intron-variant | UTP18 | GRCh38.p7 | 17:51268799 | TTATGGACATGTAGT[G/T]GTTGCCATAAATATA | 51096 |
rs772521589 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51288517 | ACACTTCATTCCTTC[A/G]CAATTTTCTTTCCTC | 51096 |
rs772541071 | snp | A/G | 0.000133074 | 0.00815593 | missense | UTP18 | GRCh38.p7 | 17:51293978 | TCTCATGTTCATACC[A/G]TGGATTTTTCTCCGA | 51096 |
rs772639505 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime | UTP18, MBTD1 | GRCh38.p7 | 17:51260425 | GGGCTGGGTAGGGGA[A/G]CGGGAGTTACGTAGA | 51096 |
rs772768638 | snp | C/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51279485 | ATATTGTGAAAAGTT[C/T]TGGGGTTTTTTTTGT | 51096 |
rs772798529 | snp | C/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51283485 | TTTTCTTATTCTGTA[C/T]GGAGTCGTTTGTGTG | 51096 |
rs772844177 | snp | C/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51280984 | GGAGTTTAAGACCAG[C/T]CTGGCCAACATGGTA | 51096 |
rs772876727 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51269173 | GTTCCTGTAGTCCCG[A/G]CTACTTGGGGGGCTG | 51096 |
rs772899735 | in-del | -/T | 4.99779e-05 | 0.00499865 | intron-variant | UTP18 | GRCh38.p7 | 17:51296948 | TGTTCAGATGACTTA[-/T]TTTTTTACTTTTCCA | 51096 |
rs772960541 | snp | A/G | 1.70548e-05 | 0.00292012 | intron-variant | UTP18 | GRCh38.p7 | 17:51277079 | GTATATACTACCAGG[A/G]TACAGGGTCTGTGGA | 51096 |
rs772962009 | snp | A/G | 3.5142e-05 | 0.00419163 | intron-variant | UTP18 | GRCh38.p7 | 17:51280507 | CATGAAAGAAGCTAA[A/G]GATATTTTTACATTT | 51096 |
rs773006121 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51272232 | GCCTCCCAAGTAGCT[A/G]GGATTACAGACATAA | 51096 |
rs773030669 | snp | A/C | 3.71892e-05 | 0.00431199 | missense, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51260859 | TGGAGCGGTGCTTGG[A/C]GGAGCTGGTCTTCGG | 51096 |
rs773049816 | snp | A/G | 1.65605e-05 | 0.0028775 | missense | UTP18 | GRCh38.p7 | 17:51285284 | ATGTGAACTCAAGGA[A/G]GTGCCTTAACAGATT | 51096 |
rs773105742 | in-del | -/CCTGGCC | | | intron-variant | UTP18 | GRCh38.p7 | 17:51264975 | ACATGAGCAACCACA[-/CCTGGCC]CCTGGCCTCGTTTCT | 51096 |
rs773143218 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51291359 | ACACTGGGGAATTTT[A/G]CAGGTAGATGCTGTT | 51096 |
rs773152859 | snp | C/G | 1.80214e-05 | 0.00300173 | intron-variant | UTP18 | GRCh38.p7 | 17:51293863 | AAGAAACATGAGCTC[C/G]CAGTTGTTACACTTT | 51096 |
rs773224745 | snp | A/G | 1.65627e-05 | 0.00287769 | missense | UTP18 | GRCh38.p7 | 17:51277209 | CTTGTTTTAGTGCTA[A/G]TGGGGAAGAAGTTTT | 51096 |
rs773250950 | snp | C/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51297119 | CCTAAGTTACTGCAT[C/T]TTTATTTAGAGGGGT | 51096 |
rs773281422 | snp | C/G | | | intron-variant, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51261843 | GCTGCTTACCAGAGC[C/G]GCCTTCGGGTGCTTG | 51096 |
rs773285121 | snp | A/C | | | intron-variant | UTP18 | GRCh38.p7 | 17:51263925 | TTTGTAAACATTTCT[A/C]CCTACTTAAAAAAAA | 51096 |
rs773331816 | snp | A/G | 8.3501e-05 | 0.00646092 | synonymous-codon | UTP18 | GRCh38.p7 | 17:51275871 | TTTCCTATAGATGAA[A/G]AACTGCCAGCATGCG | 51096 |
rs773366961 | snp | C/T | 1.70909e-05 | 0.00292321 | intron-variant | UTP18 | GRCh38.p7 | 17:51266176 | TATGCTGTTCTGTTT[C/T]TGTAGGGTTGACATG | 51096 |
rs773513273 | snp | C/T | | | downstream-variant-500B | UTP18 | GRCh38.p7 | 17:51298013 | ACTAAACATGAGAAA[C/T]TGGAAACACCTGTCT | 51096 |
rs773525710 | snp | A/G | 3.3305e-05 | 0.00408061 | missense | UTP18 | GRCh38.p7 | 17:51288159 | AATCCTACTACAGAA[A/G]TCTTGGCAATTGCTT | 51096 |
rs773562941 | snp | C/G | 1.72988e-05 | 0.00294093 | intron-variant | UTP18 | GRCh38.p7 | 17:51263396 | GGAAATGTAAGTTGC[C/G]TAACTTTTCTTCTGA | 51096 |
rs773565125 | snp | A/G | 3.6105e-05 | 0.00424867 | intron-variant | UTP18 | GRCh38.p7 | 17:51280375 | AGTTTGATAAATAAT[A/G]TTTATTGTTTTAGAC | 51096 |
rs773570316 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51273833 | CATTGGCATCAGCCT[A/G]GTTCATACTGCTGTC | 51096 |
rs773751543 | snp | C/G | | | intron-variant, downstream-variant-500B | UTP18 | GRCh38.p7 | 17:51287068 | ATTTGCCTCTATATG[C/G]GGCAAGAAAAACTGC | 51096 |
rs773777011 | in-del | -/G | | | intron-variant, downstream-variant-500B | UTP18 | GRCh38.p7 | 17:51289309 | TCAAGCGATTCTTCT[-/G]CCTCAGTCTCCTGAG | 51096 |
rs773796082 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51281146 | CACGTCTCAAAATAT[A/G]TATATATATATATAT | 51096 |
rs773796573 | snp | C/T | 2.02706e-05 | 0.00318354 | missense, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51260664 | AGCCCGGAATGAGGC[C/T]GGACTGGAAAGCCGG | 51096 |
rs773801759 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51275556 | ATGTATTTTGGGGAA[A/G]TGACTACATACTAGT | 51096 |
rs773811292 | snp | A/C | 1.66189e-05 | 0.00288256 | intron-variant | UTP18 | GRCh38.p7 | 17:51285415 | CACATTGTGCTAATG[A/C]GAATATGTTGAGGAA | 51096 |
rs773834809 | in-del | -/C | 1.66896e-05 | 0.00288869 | intron-variant | UTP18 | GRCh38.p7 | 17:51297013 | TTTGAAGTAAGAAAA[-/C]CCTTTTCTTACAAAT | 51096 |
rs773839759 | snp | G/T | | | intron-variant, missense | UTP18 | GRCh38.p7 | 17:51288548 | ATTTACCTTTTTAAG[G/T]CCTGTTGTCTTAACA | 51096 |
rs773884018 | snp | A/C | | | intron-variant | UTP18 | GRCh38.p7 | 17:51277829 | AAATTTATCTGCCCT[A/C]TACCATACCCATTCT | 51096 |
rs773892028 | snp | G/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51291312 | GTGAGATCATTGGCT[G/T]GAGGGAAGATTCACC | 51096 |
rs773899224 | snp | A/G | 6.63053e-05 | 0.00575745 | missense | UTP18 | GRCh38.p7 | 17:51273404 | TGTTGCAAAGGACTG[A/G]GAATTTCATATCCAC | 51096 |
rs773978157 | snp | C/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51292075 | ACACAGTTAAGCCAA[C/G]GTACTTATCACAAAT | 51096 |
rs773987660 | snp | A/T | 1.68863e-05 | 0.00290566 | intron-variant | UTP18 | GRCh38.p7 | 17:51273325 | AGGGGCAGCTCATTG[A/T]TTCTAAAGATCAGCC | 51096 |
rs774031761 | snp | C/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51278196 | TAAGGCAGAGCTTCT[C/T]AGAAGTAAATGTGCA | 51096 |
rs774082697 | snp | C/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51267072 | GACTCAAGAAATCCT[C/G]CCACCTCAGCCTCCC | 51096 |
rs774089194 | snp | G/T | 3.64279e-05 | 0.00426762 | missense, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51260873 | GAGGAGCTGGTCTTC[G/T]GCGACGTCGAGAACG | 51096 |
rs774179433 | snp | C/T | | | intron-variant, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51261093 | CTGCGGGTCCCTCGC[C/T]TCCCTGCTCCAGACT | 51096 |
rs774240935 | snp | A/G | | | upstream-variant-2KB, intron-variant | UTP18, MBTD1 | GRCh38.p7 | 17:51259270 | GAAGTCCACCGACTT[A/G]AAACCCTTTTAAATA | 51096 |
rs774296325 | snp | A/C | | | intron-variant | UTP18 | GRCh38.p7 | 17:51290398 | TCCAGCCTGGGTGAC[A/C]GAGTAAGAGTCTGTC | 51096 |
rs774344576 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51270452 | ATAGAACCCCACAAC[A/G]TTTTAGATTCCTGTA | 51096 |
rs774496350 | snp | A/C | 4.75885e-05 | 0.0048777 | utr-variant-5-prime, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51260552 | CGCAGCGAGGTTCCA[A/C]GTGAGCGCCTGCGTT | 51096 |
rs774524175 | in-del | -/CTG | | | upstream-variant-2KB, intron-variant | UTP18, MBTD1 | GRCh38.p7 | 17:51258907 | CCTTCCTCCACTTCC[-/CTG]CTGTTCTTTCTTGGC | 51096 |
rs774524953 | snp | C/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51275062 | ATTAGCTGGGTGTGG[C/T]GGCACATGTCTGTAA | 51096 |
rs774577783 | snp | C/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51263882 | GTATGCTTGATTTAA[C/T]ATTTTGACTTTTTCT | 51096 |
rs774740891 | snp | C/T | 4.98807e-05 | 0.00499378 | missense | UTP18 | GRCh38.p7 | 17:51293991 | CCATGGATTTTTCTC[C/T]GAGAAGTGGATACTT | 51096 |
rs774765244 | snp | C/G | 1.65537e-05 | 0.0028769 | intron-variant | UTP18 | GRCh38.p7 | 17:51277084 | TACTACCAGGATACA[C/G]GGTCTGTGGAAATAA | 51096 |
rs774781233 | snp | A/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51288404 | ATTATGTCACTTCTT[A/T]CAGTAAAGCTTTGCT | 51096 |
rs774878820 | snp | A/G/T | 3.40155e-05 | 0.00412393 | missense | UTP18 | GRCh38.p7 | 17:51280399 | TTTAGACCAAAGAAC[A/G/T]GATTGGAAGCATGAA | 51096 |
rs774886526 | snp | A/G | 1.68032e-05 | 0.0028985 | missense | UTP18 | GRCh38.p7 | 17:51266192 | TGTAGGGTTGACATG[A/G]TGAACAATCGGTTTC | 51096 |
rs774938630 | snp | A/G | 3.37371e-05 | 0.00410699 | intron-variant | UTP18 | GRCh38.p7 | 17:51275855 | AAAATCCCAGCTTTC[A/G]TTTCCTATAGATGAA | 51096 |
rs775005894 | snp | C/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51271024 | ATATTTACTGAGTTT[C/T]GTTATAAGAAAATTC | 51096 |
rs775024657 | snp | C/T | 4.49024e-05 | 0.00473806 | missense, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51260676 | GGCCGGACTGGAAAG[C/T]CGGAGCGGGGCCAGG | 51096 |
rs775140475 | snp | A/C/G | 7.36004e-05 | 0.00606596 | missense, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51260631 | TGGACCGGAGAACCG[A/C/G]AGCGAAGCCGAAGCG | 51096 |
rs775209932 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51276813 | CTTATCTGTGGGTGG[A/G]CAAACTCAAGAAATT | 51096 |
rs775248460 | snp | C/T | 1.67719e-05 | 0.0028958 | missense | UTP18 | GRCh38.p7 | 17:51288088 | TCCAAGAAACAAACC[C/T]AAAGCCAATAAAAGC | 51096 |
rs775319452 | snp | C/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51270312 | TCCATGTTTGTTTTT[C/T]AATATGTTAAACATC | 51096 |
rs775467021 | snp | C/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51296895 | TTCCTAAGTGCCCTT[C/G]TGTGATCTAATTGAA | 51096 |
rs775592075 | snp | C/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51285893 | ATTGCAGTTGAACAC[C/T]TTTTTAGCAAAGAAA | 51096 |
rs775603426 | snp | G/T | | | intron-variant, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51261947 | TTGTCGTCTGGAAAA[G/T]GAACAGTGTACGGAG | 51096 |
rs775608016 | in-del | -/GAGCGCCTGCGTTTCTCCTC | 2.34835e-05 | 0.00342655 | utr-variant-5-prime, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51260555 | AGCGAGGTTCCACGT[-/GAGCGCCTGCGTTTCTCCTC]AAACCTAACGATGCC | 51096 |
rs775663622 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51272346 | TCAGGTGATCCACTC[A/G]CCTCGGCCTCGCAAA | 51096 |
rs775678282 | snp | A/G | | | intron-variant, synonymous-codon | UTP18 | GRCh38.p7 | 17:51286633 | AGATCCCTTGGAGGG[A/G]GAGTGCCCTGATGAA | 51096 |
rs775728015 | snp | C/T | 1.66358e-05 | 0.00288402 | missense | UTP18 | GRCh38.p7 | 17:51293979 | CTCATGTTCATACCA[C/T]GGATTTTTCTCCGAG | 51096 |
rs775732765 | in-del | -/T | 1.66065e-05 | 0.00288149 | frameshift-variant | UTP18 | GRCh38.p7 | 17:51275929 | ATCTCATCTGTGCAG[-/T]TCCATCCCGGTGCAC | 51096 |
rs775740101 | snp | C/G | 1.66738e-05 | 0.00288732 | intron-variant | UTP18 | GRCh38.p7 | 17:51296945 | AAGTTGTTCAGATGA[C/G]TTATTTTTTACTTTT | 51096 |
rs775773259 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51278041 | AGAGTAGCTCTGTAC[A/G]ACCATTTTTCTACTA | 51096 |
rs775814535 | snp | G/T | 6.6246e-05 | 0.00575488 | missense | UTP18 | GRCh38.p7 | 17:51277242 | CCACGAGTACCCACA[G/T]CAAGGTTCTTTATGT | 51096 |
rs775825996 | snp | A/G | 1.66599e-05 | 0.00288611 | intron-variant | UTP18 | GRCh38.p7 | 17:51277337 | TGCACACAACCAGTC[A/G]TTCCCCCCAAGGTGA | 51096 |
rs775881265 | snp | C/T | 5.05421e-05 | 0.00502678 | intron-variant | UTP18 | GRCh38.p7 | 17:51268950 | ACATAAGTCCCTGTT[C/T]CTGTTCGTTATTATT | 51096 |
rs775902416 | snp | C/G | 3.73294e-05 | 0.00432011 | missense, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51260884 | CTTCGGCGACGTCGA[C/G]AACGACGAGGACGCG | 51096 |
rs776051492 | snp | A/G | 1.68704e-05 | 0.00290429 | missense | UTP18 | GRCh38.p7 | 17:51266187 | GTTTTTGTAGGGTTG[A/G]CATGATGAACAATCG | 51096 |
rs776083391 | snp | G/T | | | utr-variant-5-prime, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51260559 | AGGTTCCACGTGAGC[G/T]CCTGCGTTTCTCCTC | 51096 |
rs776106597 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51267009 | TTTTAAAATTTTTTT[A/G]TAGGAATGGGGTTTC | 51096 |
rs776266893 | snp | A/G | 0.000121035 | 0.00777836 | intron-variant | UTP18 | GRCh38.p7 | 17:51280493 | GGGTAAGACAACGAC[A/G]TGAAAGAAGCTAAGG | 51096 |
rs776284306 | snp | C/G | | | upstream-variant-2KB, intron-variant | UTP18, MBTD1 | GRCh38.p7 | 17:51259025 | AGGACATGAATGAGA[C/G]TGAAGGGTCTAATAA | 51096 |
rs776390129 | snp | A/G | 1.66263e-05 | 0.00288321 | missense | UTP18 | GRCh38.p7 | 17:51288145 | CTTCTCTGACCTTCA[A/G]TCCTACTACAGAAAT | 51096 |
rs776403498 | snp | A/G | 2.54159e-05 | 0.00356473 | missense, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51260681 | GACTGGAAAGCCGGA[A/G]CGGGGCCAGGCGGGC | 51096 |
rs776409656 | snp | C/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51276009 | ATGCATCTTTATTTA[C/T]TTATTTATTTCTAAT | 51096 |
rs776416413 | snp | C/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51293842 | ATAGAGTGAAGATTA[C/T]AATTTAAGAAACATG | 51096 |
rs776463800 | snp | A/T | 3.39305e-05 | 0.00411875 | missense | UTP18 | GRCh38.p7 | 17:51280401 | TAGACCAAAGAACTG[A/T]TTGGAAGCATGAAAA | 51096 |
rs776526992 | snp | G/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51292825 | TGTGTGTGTTCCTCC[G/T]CATACTTACGTCTGG | 51096 |
rs776555829 | in-del | -/A | 1.69769e-05 | 0.00291345 | intron-variant | UTP18 | GRCh38.p7 | 17:51277098 | AGGGTCTGTGGAAAT[-/A]ATCAAAAGAACCATT | 51096 |
rs776588657 | snp | G/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51274079 | CATATCAGACCTGTT[G/T]CCCATGATTTCCCAC | 51096 |
rs776614662 | snp | C/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51279543 | GTTAAAGATGAGATT[C/G]CTGTCCATCATGAGC | 51096 |
rs776654898 | snp | C/G | 1.662e-05 | 0.00288266 | intron-variant | UTP18 | GRCh38.p7 | 17:51263231 | TGTCTGCAGTCATGG[C/G]ATAGGAAAATCTCAG | 51096 |
rs776702046 | snp | C/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51284275 | CTGCAAGGAAGGATA[C/T]TGAGGTACTAGAAAA | 51096 |
rs776713949 | snp | C/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51267688 | TGTACCAGACACTGC[C/G]CCTCAAAGTCCAGTT | 51096 |
rs776728267 | snp | A/G | | | downstream-variant-500B | UTP18 | GRCh38.p7 | 17:51298193 | GTCAGTCGGCTTGAT[A/G]TGAGAGCAGTGAAAT | 51096 |
rs776749766 | in-del | -/TG | 1.67315e-05 | 0.00289231 | intron-variant | UTP18 | GRCh38.p7 | 17:51296916 | TCTAATTGAAAACAC[-/TG]TGGGTAATTACAAAG | 51096 |
rs776785125 | snp | G/T | 0.000185891 | 0.00963903 | intron-variant, missense | UTP18 | GRCh38.p7 | 17:51286582 | GCTGTGGAGCTTGGA[G/T]ACCAGGCCATCTGCC | 51096 |
rs776914137 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51285760 | AAATTAAACTTTTTT[A/G]TAGAGATGTGTGTAT | 51096 |
rs776936777 | snp | A/G | 1.66377e-05 | 0.00288419 | missense | UTP18 | GRCh38.p7 | 17:51263365 | CAGTTTGGGTGGATG[A/G]AGAAGATGAAGATGA | 51096 |
rs777073125 | in-del | -/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51279216 | TCCCTGTCTTCCTGC[-/T]TTCCTTCCTTGGAGG | 51096 |
rs777082035 | snp | C/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51281660 | AGTTTTGTGTCTTGA[C/T]TGTATCAGTGTCACT | 51096 |
rs777141164 | snp | A/G | 3.7037e-05 | 0.00430316 | missense, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51260595 | TAACGATGCCGCCGG[A/G]GCGGAGGAGACGAAT | 51096 |
rs777145575 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51297301 | ATCCACAAAAGACTT[A/G]ATAACACAGAGAGAT | 51096 |
rs777161920 | snp | A/G | 3.32469e-05 | 0.00407705 | missense | UTP18 | GRCh38.p7 | 17:51296973 | TTTCCAGGTTGCACC[A/G]TTACTCAGACTTCTA | 51096 |
rs777181283 | snp | A/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51290094 | CTGTGGTATATATAT[A/T]GGGATTCTGCATATG | 51096 |
rs777197647 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51275583 | TAGTGCTCCAAGAAT[A/G]AGTAATACATTCAGA | 51096 |
rs777283409 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51296393 | AAATAGTTGTGAAAG[A/G]AGAATATACCAGACA | 51096 |
rs777350560 | snp | C/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51263680 | CAGTTTCTAATTGAC[C/T]ATGGGCAGTTTGGAA | 51096 |
rs777379209 | snp | C/G | | | intron-variant, missense | UTP18 | GRCh38.p7 | 17:51286539 | CGTTTGCAAATTGGA[C/G]TTTGGGAGGAAAGGC | 51096 |
rs777388072 | snp | C/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51293665 | CCCAGACTTCACCAC[C/T]GTGCAAGAAATTCAT | 51096 |
rs777400353 | snp | C/T | 1.65924e-05 | 0.00288027 | missense | UTP18 | GRCh38.p7 | 17:51277299 | TTCCTGTGCATCAAG[C/T]GAGAGGTAAGATTTC | 51096 |
rs777412177 | snp | C/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51282178 | CTGCTCTGTGGGTAG[C/T]AGTCAGCAACCTCTG | 51096 |
rs777418855 | snp | A/G | 1.65938e-05 | 0.00288039 | intron-variant | UTP18 | GRCh38.p7 | 17:51285398 | GTTCTTGTAACCTTA[A/G]TCACATTGTGCTAAT | 51096 |
rs777423798 | snp | G/T | 1.87556e-05 | 0.00306226 | intron-variant | UTP18 | GRCh38.p7 | 17:51280002 | CTTCATTTCCTATTT[G/T]AGGTTTGAAAGAGAA | 51096 |
rs777487232 | snp | A/G | 4.21008e-05 | 0.00458788 | missense, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51260907 | AGGACGCGTTGCTGC[A/G]GCGTCTGCGAGGCCC | 51096 |
rs777551199 | snp | C/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51264301 | TACACCCGTCTCTGC[C/T]TCCCAAAGTGCTGAG | 51096 |
rs777584573 | snp | A/G | | | missense | UTP18 | GRCh38.p7 | 17:51263329 | ATGAAGCAAAAGGTA[A/G]TTTTCCACCTCAAAA | 51096 |
rs777670626 | snp | A/G | | | intron-variant, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51261645 | AGAGACAAGATAGAG[A/G]AGATAAACGAGTAAA | 51096 |
rs777751261 | snp | A/G | | | intron-variant, downstream-variant-500B | UTP18 | GRCh38.p7 | 17:51289392 | TTTTTTTTTTTAAGT[A/G]GAGACGGGGTTTCAC | 51096 |
rs777765512 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51287710 | TGAGATGAATGAGAC[A/G]CTAGAAGTAGGTTGG | 51096 |
rs777790506 | snp | A/G | 1.66724e-05 | 0.0028872 | missense | UTP18 | GRCh38.p7 | 17:51293952 | TCCCAGTCATTAAAA[A/G]TAAGAATATTTCTCA | 51096 |
rs777797258 | snp | A/C/T | 5.01889e-05 | 0.00500923 | intron-variant | UTP18 | GRCh38.p7 | 17:51268936 | CTGTTTAAATTAGTA[A/C/T]ATAAGTCCCTGTTCC | 51096 |
rs777909202 | snp | C/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51262561 | AATAGTAACTGGTTG[C/T]TCTTCTTGTTGGTCA | 51096 |
rs777910522 | snp | C/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51278834 | GTGGAGTGCCTTTCA[C/T]AGTAAGGAGACTAGT | 51096 |
rs777916347 | snp | C/T | 0.00010201 | 0.00714104 | missense | UTP18 | GRCh38.p7 | 17:51280477 | AAGTATACGCCTCTT[C/T]GGGTAAGACAACGAC | 51096 |
rs777948053 | snp | G/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51291083 | TGATATCTGTACACT[G/T]AACTGTCGTGATAGA | 51096 |
rs777966697 | snp | A/G | 0.000403982 | 0.0142066 | utr-variant-5-prime, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51260582 | TTCTCCTCAAACCTA[A/G]CGATGCCGCCGGAGC | 51096 |
rs777989968 | snp | G/T | 1.66308e-05 | 0.00288359 | intron-variant | UTP18 | GRCh38.p7 | 17:51285200 | TTACTTGCCTTTCAA[G/T]TTTAAAGCAAAATTA | 51096 |
rs778004025 | snp | C/T | 3.86279e-05 | 0.0043946 | intron-variant | UTP18 | GRCh38.p7 | 17:51266325 | AGAGGTGTATGTAAC[C/T]AATGCCCAGTCATTA | 51096 |
rs778041737 | in-del | -/A | 1.67253e-05 | 0.00289178 | splice-acceptor-variant | UTP18 | GRCh38.p7 | 17:51268834 | CAAATATTTTTGCTT[-/A]AGATTCCAACATGCC | 51096 |
rs778046201 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51269058 | TTGGGAGCCCGAGGC[A/G]GGTGGATCGCTTGAG | 51096 |
rs778067968 | snp | C/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51283716 | CCTCCTGGGTTCAGG[C/T]GATTCTCATGCCTCA | 51096 |
rs778110115 | snp | C/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51266790 | AAAATTAACAGTTTA[C/T]GGCTAGTCCATGTTA | 51096 |
rs778128622 | snp | G/T | | | synonymous-codon | UTP18 | GRCh38.p7 | 17:51280051 | AGTCTCCCCAGATGG[G/T]TCCTTCTTGCTCATA | 51096 |
rs778332908 | snp | C/T | | | upstream-variant-2KB, intron-variant | UTP18, MBTD1 | GRCh38.p7 | 17:51258916 | ACTTCCCTGCTGTTC[C/T]TTCTTGGCACACAAA | 51096 |
rs778453855 | snp | G/T | 0.000250106 | 0.0111799 | missense, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51260750 | CCGGCCCGGCCGAGC[G/T]CGGCGGCCGCTGCGA | 51096 |
rs778502909 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51272883 | TCATCTCCAGGGGGA[A/G]AAGCAGCCCTATTTG | 51096 |
rs778524641 | in-del | -/GGT | | | intron-variant | UTP18 | GRCh38.p7 | 17:51287962 | GGGGTTAAATCTATA[-/GGT]TTCACTTAGGTTGTG | 51096 |
rs778540539 | snp | A/G | 1.65658e-05 | 0.00287795 | missense | UTP18 | GRCh38.p7 | 17:51263298 | CATGAAGACTCGGGT[A/G]ACTCAGAAGTGGAGA | 51096 |
rs778644725 | in-del | -/TTT | | | intron-variant | UTP18 | GRCh38.p7 | 17:51282875 | TCTTCTTCTTTTTTT[-/TTT]TTTTTTTTTGAGACA | 51096 |
rs778673883 | snp | A/G | 1.72534e-05 | 0.00293708 | missense | UTP18 | GRCh38.p7 | 17:51288061 | TAAATATATACAATC[A/G]AGATTCTTGTCTCCA | 51096 |
rs778710395 | snp | A/T | | | | | GRCh38.p7 | 17:51285457 | AGGTGGTGCATGAGT[A/T]GTTCTCTTTATAAAC | 51096 |
rs778821115 | snp | G/T | | | upstream-variant-2KB, utr-variant-5-prime, intron-variant, nc-transcript-variant | UTP18, MBTD1 | GRCh38.p7 | 17:51259959 | GCGGCGACTACAGGG[G/T]GCCCCCGGCTGGGCC | 51096 |
rs778823120 | snp | A/C | 3.31779e-05 | 0.00407282 | intron-variant | UTP18 | GRCh38.p7 | 17:51263431 | CTCTGTACACTTAAA[A/C]AAGTTATTTTGCAGA | 51096 |
rs778878617 | in-del | -/TGAA | | | intron-variant | UTP18 | GRCh38.p7 | 17:51292492 | TAATATGTGACTGAC[-/TGAA]TGAAACCAGTTTAAT | 51096 |
rs778921186 | snp | C/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51286444 | TGTTGTCCAGAAACT[C/T]AGCATACTCTCTACT | 51096 |
rs778924149 | snp | C/T | 0.000320073 | 0.0126465 | intron-variant | UTP18 | GRCh38.p7 | 17:51297050 | GGTTTTAAGATACAC[C/T]CATTGCTGTCAGTTG | 51096 |
rs778938607 | snp | G/T | 9.10274e-05 | 0.00674577 | missense, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51260616 | GGAGACGAATGAAAC[G/T]GGACCGGAGAACCGG | 51096 |
rs778943576 | snp | A/G | 1.65622e-05 | 0.00287764 | synonymous-codon | UTP18 | GRCh38.p7 | 17:51285339 | ATTAAGCATTGCCAC[A/G]TCTAGGAATGGACAG | 51096 |
rs779031199 | snp | A/G | 1.66045e-05 | 0.00288132 | missense | UTP18 | GRCh38.p7 | 17:51273376 | GATGAAAGTGAAGAG[A/G]ATGAAGATGATTTGT | 51096 |
rs779045219 | snp | A/C | 1.6736e-05 | 0.0028927 | intron-variant | UTP18 | GRCh38.p7 | 17:51268940 | TTAAATTAGTACATA[A/C]GTCCCTGTTCCTGTT | 51096 |
rs779066732 | snp | C/T | | | upstream-variant-2KB, utr-variant-5-prime, intron-variant | UTP18, MBTD1 | GRCh38.p7 | 17:51260110 | CCGATTGGCCCACTT[C/T]CCTACATACCCTCCT | 51096 |
rs779093844 | snp | C/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51279625 | TGTCTCTAGTGGCAG[C/T]GTATTTCCCTTCTGG | 51096 |
rs779120237 | snp | G/T | 1.67209e-05 | 0.00289139 | intron-variant | UTP18 | GRCh38.p7 | 17:51296916 | TCTAATTGAAAACAC[G/T]GTGGGTAATTACAAA | 51096 |
rs779130260 | snp | G/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51276268 | CTGTTCACAGTTTGG[G/T]TCGCTCACCATCCCT | 51096 |
rs779135385 | snp | A/G | 1.91013e-05 | 0.00309035 | utr-variant-5-prime, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51260584 | CTCCTCAAACCTAAC[A/G]ATGCCGCCGGAGCGG | 51096 |
rs779175040 | in-del | -/A | 9.9552e-05 | 0.00705451 | intron-variant | UTP18 | GRCh38.p7 | 17:51285391 | AAGAGAGGTTCTTGT[-/A]ACCTTAATCACATTG | 51096 |
rs779190257 | snp | C/T | | | intron-variant, downstream-variant-500B | UTP18 | GRCh38.p7 | 17:51289638 | CAATTTTCTCATTCA[C/T]TTAACAATTTTTTGC | 51096 |
rs779198844 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51280607 | TCACTTGAGGTCAGC[A/G]GGTAAGATCAGCCTG | 51096 |
rs779198903 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51296119 | CCAACATACTTGGCT[A/G]TAAAACAGGAACAAA | 51096 |
rs779245180 | in-del | -/T | 0.000153776 | 0.00876725 | intron-variant | UTP18 | GRCh38.p7 | 17:51273481 | TTGGGGGATCCTATC[-/T]TAACTACTTACCTCT | 51096 |
rs779334627 | in-del | -/TCTTCCCTTTTCTTTAAGAACTG | | | intron-variant | UTP18 | GRCh38.p7 | 17:51270169 | ACTGTTTTTTCCCCT[-/TCTTCCCTTTTCTTTAAGAACTG]TTAGACAGTTTTTCC | 51096 |
rs779472821 | snp | C/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51273472 | GTCAGTGAAGTTGGG[C/G]GATCCTATCTAACTA | 51096 |
rs779475988 | in-del | -/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51289817 | CTTTGTATTAGAATA[-/T]ATCGTTTACAAAGAT | 51096 |
rs779484174 | snp | A/G | 4.42605e-05 | 0.00470407 | synonymous-codon, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51260830 | CCTGAGGCTGGAGGA[A/G]GACAAACCGGCCGTG | 51096 |
rs779505055 | snp | A/G | 4.97063e-05 | 0.00498505 | missense | UTP18 | GRCh38.p7 | 17:51277167 | AAATTCAGAGCATCT[A/G]TTTGGAAAGGTTTCC | 51096 |
rs779567924 | snp | C/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51271957 | ACAGATATGAGCCAC[C/T]ATGCCTGGCCTATTG | 51096 |
rs779574458 | in-del | -/AA | 1.86611e-05 | 0.00305454 | intron-variant | UTP18 | GRCh38.p7 | 17:51266146 | TTATATTAACTCTTT[-/AA]AAGTTATTTAAAATA | 51096 |
rs779615290 | snp | A/T | 3.90229e-05 | 0.004417 | intron-variant | UTP18 | GRCh38.p7 | 17:51288241 | ATTATTGTTATTTTT[A/T]AAATTTAAGTTGAAA | 51096 |
rs779623250 | snp | A/G | | | intron-variant, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51261690 | GTGACAAGTGCTGAA[A/G]AGAAAAAAGGACATT | 51096 |
rs779648109 | snp | C/T | | | missense | UTP18 | GRCh38.p7 | 17:51277181 | TATTTGGAAAGGTTT[C/T]CAATCTTTAAGGCTT | 51096 |
rs779661617 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51285147 | AGGTCTGTATTTGTA[A/G]TCTCCTGTACTGTTA | 51096 |
rs779701783 | snp | A/C | 1.65603e-05 | 0.00287747 | missense | UTP18 | GRCh38.p7 | 17:51293909 | CTCCTGCAGGTTCAT[A/C]TTCCTTCCTGTACAG | 51096 |
rs779805164 | snp | C/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51272697 | GGGAAGATTTTCTTA[C/T]AATTCTTTGATTTCG | 51096 |
rs779845450 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51291667 | TTGCCCCCAAGAGGC[A/G]GAGGTTACAGTGAGC | 51096 |
rs779869907 | in-del | -/CAT | | | intron-variant | UTP18 | GRCh38.p7 | 17:51293227 | TTTGAATCTCTGAGG[-/CAT]CATGCTGGATGCTGT | 51096 |
rs779923357 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51280366 | CTTTCTAACAGTTTG[A/G]TAAATAATATTTATT | 51096 |
rs779975966 | snp | A/G | 1.75096e-05 | 0.0029588 | intron-variant | UTP18 | GRCh38.p7 | 17:51266284 | ACTTAAAGAAGAGTA[A/G]GTGTCTTTTTTCATA | 51096 |
rs779982555 | snp | G/T | 0.0002086 | 0.0102106 | intron-variant | UTP18 | GRCh38.p7 | 17:51280339 | CTCTACATTGTGTGA[G/T]TCTTCTGTATACTTT | 51096 |
rs779991642 | snp | C/T | 1.72024e-05 | 0.00293273 | missense | UTP18 | GRCh38.p7 | 17:51280043 | AGCTTTGAAGTCTCC[C/T]CAGATGGGTCCTTCT | 51096 |
rs780079011 | snp | A/C | 1.65666e-05 | 0.00287802 | missense | UTP18 | GRCh38.p7 | 17:51263328 | AATGAAGCAAAAGGT[A/C]ATTTTCCACCTCAAA | 51096 |
rs780120792 | in-del | -/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51264687 | TGTTTAGTCATTGTC[-/T]TTCTTTTTTTTTTTT | 51096 |
rs780127651 | snp | G/T | | | utr-variant-3-prime | UTP18 | GRCh38.p7 | 17:51297916 | CTTAATAAACATGTG[G/T]CAGCTTTTGTTTGAA | 51096 |
rs780145973 | snp | A/G | 1.86673e-05 | 0.00305505 | synonymous-codon, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51260641 | AACCGGAGCGAAGCC[A/G]AAGCGGAAGCCCGGA | 51096 |
rs780146078 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51284070 | CATTAATGTACAGGC[A/G]GACATATAAGGCAAA | 51096 |
rs780175002 | snp | A/G | 0.000239899 | 0.0109495 | intron-variant | UTP18 | GRCh38.p7 | 17:51266150 | ATTAACTCTTTAAAA[A/G]TTATTTAAAATATGC | 51096 |
rs780188728 | snp | A/G | 0.00150615 | 0.0274008 | utr-variant-3-prime | UTP18 | GRCh38.p7 | 17:51297791 | CCTCAGGTCCAGTTG[A/G]GTCACAAGAGAAGCC | 51096 |
rs780279065 | in-del | -/AGT | 1.80263e-05 | 0.00300214 | intron-variant | UTP18 | GRCh38.p7 | 17:51293865 | GAAACATGAGCTCCC[-/AGT]TGTTACACTTTAAAG | 51096 |
rs780427398 | snp | C/T | | | intron-variant, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51262335 | GTGATCCGCCCGCCT[C/T]GGCCTCCCAAAGTGC | 51096 |
rs780437608 | snp | A/G | 1.65957e-05 | 0.00288055 | missense | UTP18 | GRCh38.p7 | 17:51273379 | GAAAGTGAAGAGGAT[A/G]AAGATGATTTGTTGC | 51096 |
rs780529427 | snp | C/G | 1.82657e-05 | 0.003022 | missense, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51260620 | ACGAATGAAACTGGA[C/G]CGGAGAACCGGAGCG | 51096 |
rs780578440 | snp | G/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51279205 | TCTGCTCTGTCTCCC[G/T]GTCTTCCTGCTTTCC | 51096 |
rs780590293 | snp | C/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51289726 | GCTATGTGTGTACTA[C/T]CAGATTGTACGCACT | 51096 |
rs780728813 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51267681 | GATGATGTGTACCAG[A/G]CACTGCCCCTCAAAG | 51096 |
rs780769034 | snp | C/T | 1.65641e-05 | 0.00287781 | missense | UTP18 | GRCh38.p7 | 17:51277194 | TTCCAATCTTTAAGG[C/T]TTGTTTTAGTGCTAA | 51096 |
rs780801096 | snp | A/C | 2.02669e-05 | 0.00318324 | utr-variant-5-prime, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51260572 | GCGCCTGCGTTTCTC[A/C]TCAAACCTAACGATG | 51096 |
rs780807399 | snp | A/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51282311 | TAAAAAGGATTAATT[A/T]TAGCTTAACATTAAT | 51096 |
rs780858977 | snp | A/C/G | 4.97511e-05 | 0.00498733 | missense | UTP18 | GRCh38.p7 | 17:51277293 | AGTTAATTCCTGTGC[A/C/G]TCAAGTGAGAGGTAA | 51096 |
rs780906046 | snp | C/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51274740 | ACAGGCGTGAGCCAC[C/T]GCGCCCAGCGACATA | 51096 |
rs780914495 | in-del | -/GGAC | | | intron-variant | UTP18 | GRCh38.p7 | 17:51287879 | GTTGGAGGTTCTATA[-/GGAC]GGACATCTGTGGCTA | 51096 |
rs780918320 | snp | C/T | | | intron-variant, downstream-variant-500B | UTP18 | GRCh38.p7 | 17:51289551 | CCTATGTAAACTCTT[C/T]TCTGCCCAACATCAG | 51096 |
rs780986830 | snp | C/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51263786 | GTACTTGTAGAACTT[C/T]TAGCACAGTGCCTGA | 51096 |
rs781102181 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51276157 | GAGTTCATTTACTTG[A/G]AAATACAAAACAGAA | 51096 |
rs781205213 | in-del | -/AGCT | | | intron-variant | UTP18 | GRCh38.p7 | 17:51282227 | TTTTTATTTGACCTC[-/AGCT]AGGAGCATTTGGTAA | 51096 |
rs781239282 | snp | C/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51264570 | AGGTGTCAGTTTCAG[C/T]CCATTCTTAGACACA | 51096 |
rs781241293 | snp | C/T | 0.000126446 | 0.00795029 | intron-variant | UTP18 | GRCh38.p7 | 17:51293856 | ACAATTTAAGAAACA[C/T]GAGCTCCCAGTTGTT | 51096 |
rs781281290 | snp | A/C/G | 4.87725e-05 | 0.00493805 | utr-variant-5-prime, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51260545 | GCGCATGCGCAGCGA[A/C/G]GTTCCACGTGAGCGC | 51096 |
rs781305711 | snp | C/T | 1.6557e-05 | 0.00287719 | synonymous-codon | UTP18 | GRCh38.p7 | 17:51280469 | TAGTAAGAAAGTATA[C/T]GCCTCTTCGGGTAAG | 51096 |
rs781313185 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51296771 | AGTAAGCCTACTCAT[A/G]TTACCTAAAATCTGA | 51096 |
rs781498730 | snp | C/T | 5.30621e-05 | 0.00515056 | missense | UTP18 | GRCh38.p7 | 17:51288052 | GTGGAGTGGTAAATA[C/T]ATACAATCAAGATTC | 51096 |
rs781560012 | snp | A/C | | | intron-variant | UTP18 | GRCh38.p7 | 17:51291874 | GTTGGTGAGTGAATG[A/C]CTGAGGCCTAGTTTC | 51096 |
rs781611657 | snp | C/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51268471 | TCTTTTAGACGTGTT[C/T]TAGTGTGTAGTCTAT | 51096 |
rs781656093 | snp | C/T | | | intron-variant, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51261571 | AGGCACTGGAGGAGA[C/T]ACAGCAATGGACAAA | 51096 |
rs781741768 | snp | A/G | 1.65798e-05 | 0.00287917 | missense | UTP18 | GRCh38.p7 | 17:51273397 | GATGATTTGTTGCAA[A/G]GGACTGGGAATTTCA | 51096 |
rs781762076 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51291167 | GTGAGGCCGAGGCAG[A/G]TGGATCACCTGAGGC | 51096 |
rs781771429 | snp | A/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51277686 | GAAACTTGGATACTC[A/T]GTAGTTTTAGTGTTA | 51096 |
rs781772564 | snp | A/C | 3.47144e-05 | 0.00416605 | intron-variant | UTP18 | GRCh38.p7 | 17:51275832 | AATGTTTATTCATTT[A/C]AATTGATAAAATCCC | 51096 |
rs796082669 | in-del | -/T | | | intron-variant, downstream-variant-500B | UTP18 | GRCh38.p7 | 17:51289201 | TTTCTGTTTTTTTTG[-/T]TTTTTTTTTTTTTGA | 51096 |
rs796095793 | in-del | -/GGAA | | | intron-variant | UTP18 | GRCh38.p7 | 17:51282524 | GAAGGAAGGAAGGAA[-/GGAA]AGAAAGAAAGAAAGA | 51096 |
rs796373857 | in-del | -/C | | | intron-variant | UTP18 | GRCh38.p7 | 17:51290165 | TCAGACCTGTAATCC[-/C]GGCACTTTGGGAGGC | 51096 |
rs796536757 | in-del | -/TT | | | intron-variant | UTP18 | GRCh38.p7 | 17:51269839 | ATATCAAATAATGTA[-/TT]GTGTGTGTGTGTGTG | 51096 |
rs796643984 | snp | C/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51284499 | TTCCTCTTCCATCAT[C/T]ATTAACATTTTGGTA | 51096 |
rs796654144 | in-del | -/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51293516 | TGTTTTTTTTTTTTT[-/T]AAGCTCATCACCTGT | 51096 |
rs796686880 | snp | C/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51272932 | TACATAGATTGCTGA[C/T]ATTGATCATTCAGCT | 51096 |
rs796702851 | snp | C/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51270855 | TCAGCAATTAGTCTG[C/T]TACAGTATGGGATAT | 51096 |