SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs725234 | snp | A/G | 0 | 0 | intron-variant | EML5 | GRCh38.p7 | 14:88748826 | acagcagctcagaca[A/G]tgatgaaaagataaa | 161436 |
rs941666 | snp | C/T | 0.49995 | 0.00499176 | intron-variant | EML5 | GRCh38.p7 | 14:88744463 | GGAACGTGACACTTA[C/T]ACAGCCTAGAAATAA | 161436 |
rs941667 | snp | A/T | 0.306679 | 0.24349 | intron-variant | EML5 | GRCh38.p7 | 14:88744540 | AATCCAAACACTGAT[A/T]TTACAGTAATTTTTT | 161436 |
rs941668 | snp | A/G | 0.365853 | 0.221536 | intron-variant | EML5 | GRCh38.p7 | 14:88621457 | CATGCAAATTTTTCT[A/G]TGACTACAGGCACAC | 161436 |
rs950388 | snp | C/T | 0.307423 | 0.243316 | intron-variant | EML5 | GRCh38.p7 | 14:88705182 | ACTGACAAATAGATA[C/T]ATAGTGTTCCAGGAA | 161436 |
rs1072353 | snp | A/G | 0.36606 | 0.221428 | intron-variant | EML5 | GRCh38.p7 | 14:88782176 | tcagatggagaagag[A/G]aacttgttgggaact | 161436 |
rs1144913 | snp | A/G | 0.368119 | 0.220336 | intron-variant | EML5 | GRCh38.p7 | 14:88622895 | GATATACTATATCTC[A/G]GTCAAAATAAACATC | 161436 |
rs1144914 | snp | A/T | 0.182933 | 0.240836 | intron-variant | EML5 | GRCh38.p7 | 14:88624209 | AGCCTCCTGAGTAGC[A/T]GGGACTACAGGCATG | 161436 |
rs1144915 | snp | C/T | 0.499994 | 0.00179711 | intron-variant | EML5 | GRCh38.p7 | 14:88624479 | TCAGAAGAGACCTCT[C/T]CTCAAATTTTGAGGT | 161436 |
rs1144916 | snp | C/G | 0.294775 | 0.245958 | intron-variant | EML5 | GRCh38.p7 | 14:88627899 | TATGCATATTCATCT[C/G]TGAAACATGGACAAA | 161436 |
rs1144917 | snp | C/T | 0.294576 | 0.245994 | intron-variant | EML5 | GRCh38.p7 | 14:88628908 | AATATCAAAACTACA[C/T]GGAAACATACATAAA | 161436 |
rs1144918 | snp | C/T | 0.364817 | 0.222075 | intron-variant | EML5 | GRCh38.p7 | 14:88636214 | agggccattagtagg[C/T]tcaggaccatctggt | 161436 |
rs1144919 | snp | C/T | 0.29432 | 0.24604 | intron-variant | EML5 | GRCh38.p7 | 14:88639461 | TCTGTTTTGGTTTCT[C/T]AAAGAAAAGGATTTG | 161436 |
rs1144920 | snp | G/T | 0.077417 | 0.180873 | intron-variant | EML5 | GRCh38.p7 | 14:88640397 | tcaataccaagaaga[G/T]ctcccaaaaccacac | 161436 |
rs1144921 | snp | A/G | 0.294576 | 0.245994 | intron-variant | EML5 | GRCh38.p7 | 14:88643951 | GATTATGAAATGCCT[A/G]AAGAGCCTTCCTTCT | 161436 |
rs1144922 | snp | A/G | 0.365439 | 0.221752 | intron-variant | EML5 | GRCh38.p7 | 14:88646364 | TTCAAGAATATATAA[A/G]CAATGTTTTCAAACC | 161436 |
rs1152379 | snp | C/T | 0 | 0 | intron-variant | EML5 | GRCh38.p7 | 14:88625370 | TAGACAATTCTTCCC[C/T]TCCAATTCTAACATA | 161436 |
rs1152380 | snp | A/C | 0.0182019 | 0.0936463 | intron-variant | EML5 | GRCh38.p7 | 14:88627333 | ATTAGAAATATACAT[A/C]ATTTTCATAAGAATC | 161436 |
rs1152381 | snp | G/T | 0.294832 | 0.245947 | intron-variant | EML5 | GRCh38.p7 | 14:88630341 | GGCCTAATAAAAACT[G/T]TATTTTAAAAGAAAA | 161436 |
rs1152382 | snp | A/G | 0.163564 | 0.234582 | intron-variant | EML5 | GRCh38.p7 | 14:88638411 | TAGAACCCTGCTTCC[A/G]TGGGGGTTCAGGCTG | 161436 |
rs1152383 | snp | A/T | 0.462308 | 0.132005 | intron-variant | EML5 | GRCh38.p7 | 14:88638943 | ATTAAGTTTGAAAAT[A/T]TTAAGATGTAACAGC | 161436 |
rs1152384 | snp | A/C | 0.368324 | 0.220226 | intron-variant | EML5 | GRCh38.p7 | 14:88645334 | cacagccTTACTTTT[A/C]ATTTCTTTGGTGTAC | 161436 |
rs1152385 | snp | G/T | 0.293294 | 0.246223 | intron-variant | EML5 | GRCh38.p7 | 14:88648094 | TTTAAAAAGTTTTTT[G/T]TCTCTCTTAATAGCA | 161436 |
rs1152386 | snp | C/T | 0.184521 | 0.241273 | intron-variant | EML5 | GRCh38.p7 | 14:88649336 | CCACAATTACAGGCC[C/T]GAGCCACCGTGCCCA | 161436 |
rs1152387 | snp | C/T | 0.184203 | 0.241186 | intron-variant | EML5 | GRCh38.p7 | 14:88653157 | tcttgtatcctgaga[C/T]tttgctgaacttgct | 161436 |
rs1152388 | snp | C/T | 0.0547245 | 0.156101 | intron-variant | EML5 | GRCh38.p7 | 14:88653724 | tgaggactttcacat[C/T]gatgtttaccaggca | 161436 |
rs1287678 | snp | G/T | | | intron-variant | EML5 | GRCh38.p7 | 14:88659337 | tgtattcccagctac[G/T]tgggaggctgaggta | 161436 |
rs1287679 | snp | A/G | 0.184521 | 0.241273 | intron-variant | EML5 | GRCh38.p7 | 14:88659330 | CCAGCTACTTGGGAG[A/G]CTGAGGTAGAAGAAT | 161436 |
rs1287680 | snp | A/G | 0.362523 | 0.223246 | intron-variant | EML5 | GRCh38.p7 | 14:88654528 | actgggtaaataaca[A/G]aattaaggcagaaat | 161436 |
rs1287681 | snp | G/T | 0.163236 | 0.234461 | intron-variant | EML5 | GRCh38.p7 | 14:88654298 | aagacaagaaataaa[G/T]atcagagcacaactg | 161436 |
rs1287682 | snp | C/T | 0.030665 | 0.119967 | intron-variant | EML5 | GRCh38.p7 | 14:88651131 | CAAGGCAGAAGTCAT[C/T]AATGTGATTTCATTT | 161436 |
rs1287683 | snp | A/G | 0.304937 | 0.243889 | intron-variant | EML5 | GRCh38.p7 | 14:88650174 | tgagccaccttgccc[A/G]gccAATAAATGTTTT | 161436 |
rs1287801 | snp | C/T | 0.499999 | 0.000599041 | intron-variant | EML5 | GRCh38.p7 | 14:88634109 | cctggtgggaggtga[C/T]tggatcatgggggca | 161436 |
rs1287825 | snp | A/G | 0.32153 | 0.239548 | intron-variant | EML5 | GRCh38.p7 | 14:88639192 | GAGCAGAAAAGATTA[A/G]TCTCATCATGGGAAT | 161436 |
rs1297872 | snp | C/T | 0.365559 | 0.224119 | intron-variant | EML5 | GRCh38.p7 | 14:88663908 | AACAATTTTTTTGCA[C/T]AATATTTAAATCACT | 161436 |
rs1299425 | snp | A/G | 0.360421 | 0.224293 | intron-variant | EML5 | GRCh38.p7 | 14:88650870 | tggtgctaaacacct[A/G]gtctcaagcagtcct | 161436 |
rs1950804 | snp | A/T | | | intron-variant | EML5 | GRCh38.p7 | 14:88727889 | tgctagaaatcatca[A/T]caaaaaagataacta | 161436 |
rs1950805 | snp | A/G | 0.376989 | 0.215346 | intron-variant | EML5 | GRCh38.p7 | 14:88774093 | actgcactccagcct[A/G]ggtgacgagagcgag | 161436 |
rs1950806 | snp | C/T | 0.304188 | 0.244057 | intron-variant | EML5 | GRCh38.p7 | 14:88774412 | AGTTATACATTGGAA[C/T]GAATCTTGAAAGAGG | 161436 |
rs1956406 | snp | C/T | 0.384401 | 0.210799 | intron-variant | EML5 | GRCh38.p7 | 14:88749711 | GAAGATCACAAAAAT[C/T]TGGATTACAAAGTGT | 161436 |
rs1956407 | snp | C/T | 0.232359 | 0.249377 | intron-variant | EML5 | GRCh38.p7 | 14:88751448 | GGGAGGGAAGGAGTG[C/T]TAACTGGAAAGCGGC | 161436 |
rs1956408 | snp | A/T | 0 | 0 | intron-variant | EML5 | GRCh38.p7 | 14:88751695 | CCAGAGAATGTAAGT[A/T]AAGTGAAAAGAAAAG | 161436 |
rs1956409 | snp | G/T | 0.366473 | 0.221211 | intron-variant | EML5 | GRCh38.p7 | 14:88755616 | CAATTTACAATATCA[G/T]ATTTGCCCTTGAGAT | 161436 |
rs1956410 | snp | A/G | 0.366266 | 0.221319 | intron-variant | EML5 | GRCh38.p7 | 14:88764020 | cttttcttctttagc[A/G]attatatagcgaatt | 161436 |
rs1956411 | snp | C/T | 0.36021 | 0.224397 | intron-variant | EML5 | GRCh38.p7 | 14:88668016 | TCTGGCAAGCTTTTT[C/T]GCCACAAGCTCACTG | 161436 |
rs1956412 | snp | C/T | 0.0460142 | 0.144533 | intron-variant | EML5 | GRCh38.p7 | 14:88685453 | CCCTCTTATTTACAA[C/T]ATTCTTATTAGTAAT | 161436 |
rs2033416 | snp | C/T | 0.306182 | 0.243605 | intron-variant | EML5 | GRCh38.p7 | 14:88660184 | GTTATCCTCCCACCT[C/T]AGCCTCTTGAGTAAC | 161436 |
rs2033417 | snp | A/G | 0.376791 | 0.215463 | intron-variant | EML5 | GRCh38.p7 | 14:88652347 | CCCCCGCGTTGCCAG[A/G]GAAGTCTAGATGGAG | 161436 |
rs2093084 | snp | A/G | 0.499965 | 0.00419314 | intron-variant | EML5 | GRCh38.p7 | 14:88721568 | tggccagctatatgc[A/G]gaaaactgaaactgg | 161436 |
rs2145119 | snp | C/G | 0.366473 | 0.221211 | intron-variant, upstream-variant-2KB | EML5 | GRCh38.p7 | 14:88768596 | tttgtatttttagta[C/G]agacggggttccacc | 161436 |
rs2145120 | snp | A/G | 0.377582 | 0.214995 | intron-variant | EML5 | GRCh38.p7 | 14:88777699 | GCAGGAGGATGGGCC[A/G]GGCACAGTGGCTCAT | 161436 |
rs2180593 | snp | C/T | | | intron-variant | EML5 | GRCh38.p7 | 14:88666703 | AAATAAGGGTTAGTG[C/T]TGCATTGATAAACAC | 161436 |
rs2180594 | snp | A/G | 0.0333695 | 0.124785 | intron-variant | EML5 | GRCh38.p7 | 14:88701603 | AAAGGAAGAAGAATG[A/G]GAGAAAGAAAAAAGG | 161436 |
rs2224333 | snp | C/T | 0.384401 | 0.210799 | intron-variant, upstream-variant-2KB | EML5 | GRCh38.p7 | 14:88768748 | CTCTCTTTTCTTCAA[C/T]ATTTATTAATTAGAA | 161436 |
rs2401745 | snp | C/T | 0.49995 | 0.00499176 | intron-variant | EML5 | GRCh38.p7 | 14:88743170 | CCTCCTCTCTAGTTA[C/T]AATTTTGTATCCTTT | 161436 |
rs2401746 | snp | A/T | 0.499982 | 0.00299515 | intron-variant | EML5 | GRCh38.p7 | 14:88727367 | gatgcagagttgaga[A/T]gttgggaaagagatg | 161436 |
rs2401747 | snp | A/T | 0.363359 | 0.222822 | intron-variant | EML5 | GRCh38.p7 | 14:88692668 | TGCAAATTCGCAGCA[A/T]ATACTAcagttgtac | 161436 |
rs2401748 | snp | A/G | 0.364609 | 0.222182 | intron-variant | EML5 | GRCh38.p7 | 14:88692308 | ctcactacaacctcc[A/G]cctcctgggttcaag | 161436 |
rs2401749 | snp | C/T | 0.365439 | 0.221752 | intron-variant | EML5 | GRCh38.p7 | 14:88680801 | CCATGATGTCTGGAT[C/T]GAGGGTGTGGGAATC | 161436 |
rs2567888 | snp | A/G | 0 | 0 | | | GRCh38.p7 | 14:88660094 | gagatggggtctcca[A/G]atgttgcctatgctg | 161436 |
rs2896075 | snp | C/T | 0.376791 | 0.215463 | intron-variant | EML5 | GRCh38.p7 | 14:88782163 | TTTCTCTTCTCCATC[C/T]GAGACCACCTCAGGG | 161436 |
rs2896076 | snp | C/T | 0 | 0 | intron-variant, upstream-variant-2KB | EML5 | GRCh38.p7 | 14:88768274 | agcatacttagtgac[C/T]acaaagaaaaacttt | 161436 |
rs2896077 | snp | G/T | 0 | 0 | intron-variant | EML5 | GRCh38.p7 | 14:88627557 | TTGTCTTAAAGTTGG[G/T]GGTTGAAACAATCAT | 161436 |
rs2915568 | snp | A/G | 0 | 0 | intron-variant | EML5 | GRCh38.p7 | 14:88622725 | TCTTTTGACCTAAGT[A/G]AATAACCAAGCCAGA | 161436 |
rs2983488 | snp | C/G | 0 | 0 | intron-variant | EML5 | GRCh38.p7 | 14:88622044 | CTCCCCCTCCCCCTT[C/G]TCCGCCTCCAGTAAC | 161436 |
rs3055841 | in-del | -/AA | 0.460252 | 0.135255 | intron-variant | EML5 | GRCh38.p7 | 14:88727401 | aaaaaaaaaaaaaaa[-/AA]TGCAGTGTAtcacac | 161436 |
rs3220543 | microsatellite | (CA)19/20/21/23/24/25/26/29/30 | 0.72231 | 0.145421 | intron-variant | EML5 | GRCh38.p7 | 14:88745160 | CAGAGAGGCCTATTA[(CA)19/20/21/23/24/25/26/29/30]ANTTTAGACCATTAT | 161436 |
rs3825675 | snp | A/G | 0 | 0 | utr-variant-3-prime, nc-transcript-variant | ZC3H14 | GRCh38.p7 | 14:88613357 | TATTTAAACAATTTA[A/G]AATAAATTTCTTCTG | 161436 |
rs4243685 | snp | C/T | 0.384017 | 0.211044 | intron-variant | EML5 | GRCh38.p7 | 14:88692703 | CAAGTGACTAAGGTG[C/T]CCAAATGAAGTTTGT | 161436 |
rs4265742 | snp | A/G | 0.373799 | 0.217195 | intron-variant | EML5 | GRCh38.p7 | 14:88692379 | gagactctgtttcaa[A/G]aagaaaaaaaggatg | 161436 |
rs4365227 | snp | A/G | 0.366679 | 0.221102 | intron-variant | EML5 | GRCh38.p7 | 14:88719724 | GGACAGCAAAATGGT[A/G]GAAAAGGACTTTCCA | 161436 |
rs4451888 | snp | A/T | 0.0836354 | 0.186609 | intron-variant | EML5 | GRCh38.p7 | 14:88738469 | GTGAAGGAAAAATAC[A/T]CCTATCCACATTTAA | 161436 |
rs4548803 | snp | A/G | 0.449979 | 0.150028 | intron-variant | EML5 | GRCh38.p7 | 14:88728334 | aatgcaccagttaga[A/G]gcaccaattcccatg | 161436 |
rs4569185 | snp | C/G | 0 | 0 | intron-variant | EML5 | GRCh38.p7 | 14:88721402 | caaaacagcatgatg[C/G]tggtataaaaacaga | 161436 |
rs4635267 | snp | C/T | 0.36254 | 0.223341 | intron-variant | EML5 | GRCh38.p7 | 14:88621922 | GAAAATACATAAATA[C/T]GTGATTCTTAACTAT | 161436 |
rs4899957 | snp | C/G | 0.3748 | 0.216622 | intron-variant | EML5 | GRCh38.p7 | 14:88635266 | ATATTGATAACATAG[C/G]ACCATAGTGCCTTGA | 161436 |
rs4899958 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EML5 | GRCh38.p7 | 14:88671992 | TCAACATTAGATCAT[A/C]AAGACAGAAAATTAA | 161436 |
rs4899959 | snp | G/T | 0.232651 | 0.249397 | intron-variant | EML5 | GRCh38.p7 | 14:88678946 | ATGTTGGCAGAGCTA[G/T]GCTCCGTTGTGAAAG | 161436 |
rs4904463 | snp | A/G | 0.371987 | 0.218218 | intron-variant | EML5 | GRCh38.p7 | 14:88693371 | GAGGAGCAAAGTCAC[A/G]TCTTACATGGTGACA | 161436 |
rs4904464 | snp | A/C | 0.375797 | 0.216044 | intron-variant | EML5 | GRCh38.p7 | 14:88728788 | AATGAACTTGAACAT[A/C]CACAGATTATGGTAT | 161436 |
rs4904465 | snp | A/G | 0.499968 | 0.00399348 | intron-variant | EML5 | GRCh38.p7 | 14:88732385 | GGTTGTAGATGTGTG[A/G]TATTATTTCTGAGGG | 161436 |
rs4904466 | snp | C/T | 0.29432 | 0.24604 | intron-variant | EML5 | GRCh38.p7 | 14:88749666 | GAATATACTTTTTCA[C/T]ATTCTTTCCAAATAT | 161436 |
rs4904467 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | EML5 | GRCh38.p7 | 14:88753100 | ttaagctgctggtgt[C/T]aaagaatattgtttg | 161436 |
rs5001166 | snp | A/G | | | intron-variant | EML5 | GRCh38.p7 | 14:88683094 | TTTTGAAAATTTCTT[A/G]ACTATTCTTGAATAT | 161436 |
rs5001167 | snp | A/G | 0.5 | 0 | intron-variant | EML5 | GRCh38.p7 | 14:88683151 | CTTTCCAGAATTTGT[A/G]AAAAATCTAATAAAA | 161436 |
rs5016580 | snp | C/T | 0.373799 | 0.217195 | intron-variant | EML5 | GRCh38.p7 | 14:88681365 | CCTGTGATCCCACCA[C/T]TTTGGCAGGCCGAGG | 161436 |
rs5810420 | in-del | -/A | 0.546236 | 0.104291 | intron-variant | EML5 | GRCh38.p7 | 14:88662286 | AAATAAAAAAAAAAA[-/A]GGCTAATATTGTCAG | 161436 |
rs5810422 | in-del | -/A/AA | 0.457853 | 0.138915 | intron-variant | EML5 | GRCh38.p7 | 14:88724114 | TACAAAAAAAAAAAA[-/A/AA]TAGCTTGGCGTGGTG | 161436 |
rs5810423 | in-del | -/GAGTT | 0.376394 | 0.215696 | intron-variant | EML5 | GRCh38.p7 | 14:88751615 | CAAGTGTGATATTTA[-/GAGTT]GAGAAGCCAGAGCCA | 161436 |
rs6575016 | snp | C/T | 0.184203 | 0.241186 | intron-variant | EML5 | GRCh38.p7 | 14:88669190 | tcaggagatcccctc[C/T]gtgagcccatgccac | 161436 |
rs6575018 | snp | C/T | 0.3744 | 0.216852 | intron-variant | EML5 | GRCh38.p7 | 14:88696199 | TATTTCCCTCTGAAC[C/T]CTACTATGGATAATT | 161436 |
rs6575019 | snp | A/G | 0.499954 | 0.00479211 | intron-variant | EML5 | GRCh38.p7 | 14:88761813 | tttacactcccacca[A/G]tgtaaaagtgtccct | 161436 |
rs6575020 | snp | C/T | 0.365024 | 0.221967 | intron-variant | EML5 | GRCh38.p7 | 14:88788980 | AGGTGGGATGATCAC[C/T]TGAGCCCAAGATTTC | 161436 |
rs7140678 | snp | A/G | 0.377187 | 0.215229 | intron-variant, upstream-variant-2KB | EML5 | GRCh38.p7 | 14:88766498 | CAGGCTTATTGGGAC[A/G]AGGAAATTCCTGCCT | 161436 |
rs7140849 | snp | G/T | 0.365439 | 0.221752 | intron-variant, upstream-variant-2KB | EML5 | GRCh38.p7 | 14:88766553 | TCTGCTCTCAAACCC[G/T]GTCTCCTGATGTTAC | 161436 |
rs7141671 | snp | C/T | 0.366679 | 0.221102 | intron-variant, upstream-variant-2KB | EML5 | GRCh38.p7 | 14:88766509 | GGACGAGGAAATTCC[C/T]GCCTAATAAATTTTG | 161436 |
rs7142113 | snp | C/G | 0.169435 | 0.236663 | intron-variant | EML5 | GRCh38.p7 | 14:88712120 | AAATGCAGCATATGA[C/G]AATAATTTTTGAATT | 161436 |
rs7142601 | snp | A/G | 0.316485 | 0.240998 | intron-variant | EML5 | GRCh38.p7 | 14:88696584 | AGATGAATTTAGGTT[A/G]TTACGTAGATAAACA | 161436 |
rs7142842 | snp | C/T | 0.306927 | 0.243432 | intron-variant | EML5 | GRCh38.p7 | 14:88745456 | CTGGCTATGATGTAT[C/T]GTTTATATACAATTT | 161436 |
rs7144251 | snp | C/T | 0.325563 | 0.238307 | intron-variant | EML5 | GRCh38.p7 | 14:88724595 | CACTACTTTTGAATG[C/T]GTATCAGATATGATA | 161436 |
rs7144932 | snp | C/G | 0.499996 | 0.00139776 | intron-variant | EML5 | GRCh38.p7 | 14:88758093 | aacttttgggcttaa[C/G]agatcctcccacctc | 161436 |
rs7145378 | snp | A/G | 0.376394 | 0.215696 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | EML5 | GRCh38.p7 | 14:88766758 | CTTACCAGTTTTGCA[A/G]CTTGAGGGGCATCAC | 161436 |
rs7145387 | snp | A/G | 0.0170251 | 0.090679 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | EML5 | GRCh38.p7 | 14:88766774 | CTTGAGGGGCATCAC[A/G]GAACCTGCCAACATG | 161436 |
rs7146297 | snp | A/C | 0.317451 | 0.240729 | intron-variant | EML5 | GRCh38.p7 | 14:88619494 | acaggtgtgagccac[A/C]acacccagTCAGAAC | 161436 |
rs7146379 | snp | C/T | 0.146985 | 0.227789 | intron-variant | EML5 | GRCh38.p7 | 14:88783123 | aaagaaaagaaaatg[C/T]ctggacgtccaggta | 161436 |
rs7146508 | snp | A/G | 0.366266 | 0.221319 | intron-variant | EML5 | GRCh38.p7 | 14:88696634 | ATGTAAATTTTAATA[A/G]GTATTAAAACTATAC | 161436 |
rs7146735 | snp | G/T | 0.499997 | 0.00119808 | intron-variant, upstream-variant-2KB | EML5 | GRCh38.p7 | 14:88766956 | AATGTTTTACATTCT[G/T]TCATAAATTCAACAT | 161436 |
rs7147032 | snp | A/T | | | intron-variant | EML5 | GRCh38.p7 | 14:88649212 | tatttttacttttat[A/T]ttttgtagagacagg | 161436 |
rs7147796 | snp | C/G | 0.367708 | 0.220556 | intron-variant | EML5 | GRCh38.p7 | 14:88762225 | agaaacttacaaaga[C/G]acgggccatgcgtag | 161436 |
rs7148308 | snp | C/G | 0.365439 | 0.221752 | intron-variant | EML5 | GRCh38.p7 | 14:88762366 | aaataaaaaattagc[C/G]ggttgtggtggcaca | 161436 |
rs7149053 | snp | C/T | 0 | 0 | intron-variant | EML5 | GRCh38.p7 | 14:88697243 | TGAATATCTATTGTT[C/T]GTATGCTAGATACAA | 161436 |
rs7149465 | snp | C/T | 0.307176 | 0.243374 | intron-variant | EML5 | GRCh38.p7 | 14:88780043 | tgtaacctccacctc[C/T]caggttcaagagatt | 161436 |
rs7149523 | snp | C/T | 0.307919 | 0.243198 | intron-variant | EML5 | GRCh38.p7 | 14:88692245 | agctgggtgtggtgg[C/T]gggcacctgtaatcc | 161436 |
rs7149951 | snp | C/T | 0.386884 | 0.209196 | intron-variant | EML5 | GRCh38.p7 | 14:88662407 | AACAAACTTCTTAGG[C/T]ATATGGATTCCTAAG | 161436 |
rs7151649 | snp | C/T | | | intron-variant | EML5 | GRCh38.p7 | 14:88759517 | agcaagaccccacct[C/T]tacaaaaaataaaac | 161436 |
rs7153044 | snp | A/G | 0.499958 | 0.00459246 | intron-variant | EML5 | GRCh38.p7 | 14:88697897 | TGTGCCACCACACCC[A/G]GCTAATTTTTTGTAT | 161436 |
rs7153778 | snp | C/G | 0.499965 | 0.00419314 | intron-variant | EML5 | GRCh38.p7 | 14:88785821 | ttccatcctgcccct[C/G]cctctcttcagtctg | 161436 |
rs7154157 | snp | C/T | 0.384593 | 0.210677 | intron-variant | EML5 | GRCh38.p7 | 14:88762672 | agacctaacagacat[C/T]gacagaactctccac | 161436 |
rs7154513 | snp | A/G | 0 | 0 | intron-variant | EML5 | GRCh38.p7 | 14:88692683 | ATGCTGCGAATTTGC[A/G]ATTACAAGTGACTAA | 161436 |
rs7154735 | snp | G/T | 0.189576 | 0.242588 | intron-variant | EML5 | GRCh38.p7 | 14:88756238 | ggcatattaacagaa[G/T]aaaggtcaaaaaaac | 161436 |
rs7155614 | snp | A/G | 0.366679 | 0.221102 | intron-variant | EML5 | GRCh38.p7 | 14:88742535 | TATTTAGTTTGAGAT[A/G]AGCTTTTTATAAAAA | 161436 |
rs7155837 | snp | A/C | 0.039522 | 0.134904 | intron-variant | EML5 | GRCh38.p7 | 14:88713785 | AAAATCTTTGGTTGC[A/C]ATTCTGTTTTTCAAA | 161436 |
rs7156054 | snp | A/G | 0.367913 | 0.220446 | intron-variant | EML5 | GRCh38.p7 | 14:88617399 | tgatcacccccgctc[A/G]gcctcccaaagtgct | 161436 |
rs7156169 | snp | A/C/T | | | intron-variant | EML5 | GRCh38.p7 | 14:88759683 | ggcaagtcaccatct[A/C/T]ttaaaaaaaaaaaaa | 161436 |
rs7156823 | snp | A/G | 0.377187 | 0.215229 | intron-variant | EML5 | GRCh38.p7 | 14:88774305 | GAAGCAACGATCCAG[A/G]GCTGCCAGCTATGTG | 161436 |
rs7157149 | snp | C/T | 0.384017 | 0.211044 | intron-variant, utr-variant-5-prime | EML5 | GRCh38.p7 | 14:88765501 | aatctttctgacttc[C/T]gctgcatgttttctc | 161436 |
rs7160305 | snp | A/G | 0.366266 | 0.221319 | intron-variant | EML5 | GRCh38.p7 | 14:88772848 | TACACTGGCCTTTCT[A/G]TCCCTTAAAATGGCC | 161436 |
rs7160983 | snp | C/T | 0.367091 | 0.220884 | intron-variant | EML5 | GRCh38.p7 | 14:88787577 | ACACATCTATTACAA[C/T]TTCAACTATTATTCT | 161436 |
rs7161635 | snp | C/T | 0.376394 | 0.215696 | intron-variant, upstream-variant-2KB | EML5 | GRCh38.p7 | 14:88766286 | TGCCTGAGAGCTGGG[C/T]GGAACAGAGCCATAT | 161436 |
rs7400729 | snp | A/G | 0.372189 | 0.218105 | intron-variant | EML5 | GRCh38.p7 | 14:88672636 | gaaaaaaattaataa[A/G]atagatcattagcta | 161436 |
rs7400757 | snp | A/G | 0.374 | 0.217081 | intron-variant | EML5 | GRCh38.p7 | 14:88672701 | taaaaaatgataaag[A/G]ggacatcaccactga | 161436 |
rs8003018 | snp | C/T | 0.366473 | 0.221211 | intron-variant | EML5 | GRCh38.p7 | 14:88736225 | AGGATGGTCTCAATC[C/T]CTTGACCTTGTGATC | 161436 |
rs8004073 | snp | G/T | | | intron-variant | EML5 | GRCh38.p7 | 14:88745163 | AATGGTCTAAATtgt[G/T]tgtttgtgtgtgtgt | 161436 |
rs8004599 | snp | C/T | 0.367091 | 0.220884 | intron-variant | EML5 | GRCh38.p7 | 14:88723992 | TAATATGTTATGAGC[C/T]GGGCACAGTAGCTCA | 161436 |
rs8005549 | snp | A/G | 0.362523 | 0.223246 | intron-variant | EML5 | GRCh38.p7 | 14:88666588 | TAGGAAGATACATCT[A/G]TATATATACGTTTCA | 161436 |
rs8005930 | snp | C/T | 0.362313 | 0.223351 | intron-variant | EML5 | GRCh38.p7 | 14:88666257 | TTGAGATGGAATTTC[C/T]CTCTTGTTGCCCAGG | 161436 |
rs8006652 | snp | C/T | 0.380333 | 0.213338 | intron-variant | EML5 | GRCh38.p7 | 14:88631290 | gtgatcatgacacac[C/T]gcagcctcgaattcc | 161436 |
rs8006786 | snp | A/C/T | 0.00875054 | 0.0656008 | intron-variant | EML5 | GRCh38.p7 | 14:88631338 | cctacctcaaccttc[A/C/T]gagtagctggatcta | 161436 |
rs8007084 | snp | C/G | 0.365439 | 0.221752 | intron-variant | EML5 | GRCh38.p7 | 14:88719318 | TTGAGCCCAGGAGTT[C/G]GAGGCTGCAGTGAGC | 161436 |
rs8008847 | snp | A/G | 0.163236 | 0.234461 | utr-variant-3-prime, nc-transcript-variant | ZC3H14 | GRCh38.p7 | 14:88612583 | TATAAATGTACATAT[A/G]TATTCTCACATTCTG | 161436 |
rs8010841 | snp | A/G | 0.159622 | 0.233092 | upstream-variant-2KB | EML5 | GRCh38.p7 | 14:88793903 | AAAGTATTGGGAACA[A/G]TCAATTCCTGACTAT | 161436 |
rs8013590 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EML5 | GRCh38.p7 | 14:88685187 | GACATACAGTTACTA[C/T]AATACAACAGTGTAT | 161436 |
rs8016561 | snp | A/G | 0.499035 | 0.0219437 | upstream-variant-2KB | EML5 | GRCh38.p7 | 14:88793498 | CCCGCCTCAGTCTCC[A/G]GAGTAGTAAGGAGTA | 161436 |
rs8017299 | snp | A/T | 0.394721 | 0.203852 | intron-variant | EML5 | GRCh38.p7 | 14:88717505 | GGCTCACGCCTGTAA[A/T]CCCAGCAGTTTGGGA | 161436 |
rs8017313 | snp | C/T | 0.366679 | 0.221102 | intron-variant | EML5 | GRCh38.p7 | 14:88765145 | accataaatttagca[C/T]cttaaagcaatacaa | 161436 |
rs8018076 | snp | C/T | 0.0637235 | 0.166737 | intron-variant | EML5 | GRCh38.p7 | 14:88707200 | TATACACCCAATTTC[C/T]CCAATAATAAAGGAA | 161436 |
rs8018630 | snp | A/C | 0.377977 | 0.21476 | intron-variant | EML5 | GRCh38.p7 | 14:88714250 | TTTTGACTAAGATAC[A/C]GTGGTACTTTACCAT | 161436 |
rs8018755 | snp | C/T | 0.377977 | 0.21476 | intron-variant | EML5 | GRCh38.p7 | 14:88714249 | TTTTTGACTAAGATA[C/T]AGTGGTACTTTACCA | 161436 |
rs8020072 | snp | C/T | 0.378174 | 0.214642 | intron-variant | EML5 | GRCh38.p7 | 14:88714332 | CTCCAGCCAAAGCAG[C/T]TTTAATTAagaacca | 161436 |
rs8021690 | snp | C/T | 0.371582 | 0.218444 | intron-variant | EML5 | GRCh38.p7 | 14:88717806 | caaATTAAAGGAGCA[C/T]AGTAATAGGATCAAA | 161436 |
rs8021906 | snp | C/G | 0.152667 | 0.230274 | intron-variant | EML5 | GRCh38.p7 | 14:88726876 | AGAATCTTTTGCTTT[C/G]AAtttttttggcgac | 161436 |
rs8023218 | snp | A/G | 0.0399052 | 0.1355 | intron-variant | EML5 | GRCh38.p7 | 14:88736073 | tgccatgatcttggc[A/G]cactgcaaccttcgc | 161436 |
rs9323832 | snp | C/T | 0.029116 | 0.117091 | intron-variant | EML5 | GRCh38.p7 | 14:88617604 | tgagatccctatctc[C/T]acaaaaataaaaatG | 161436 |
rs9671509 | snp | C/T | 0.366679 | 0.221102 | intron-variant | EML5 | GRCh38.p7 | 14:88747061 | ACCGCAACTTTGATC[C/T]ATCCCTCAAAGAATT | 161436 |
rs9707245 | snp | A/G | 0.366885 | 0.220993 | intron-variant | EML5 | GRCh38.p7 | 14:88731208 | atatctcctaatgtt[A/G]tccctcccccctccc | 161436 |
rs9750095 | snp | A/G | 0.5 | 0 | intron-variant | EML5 | GRCh38.p7 | 14:88721232 | GTGAAGAAAGTCATT[A/G]GTAGCTTGATGGGGA | 161436 |
rs9796339 | snp | A/T | | | intron-variant | EML5 | GRCh38.p7 | 14:88639748 | tgcccagctatatat[A/T]ttttgtatttttagt | 161436 |
rs10129842 | snp | C/T | 0.366679 | 0.221102 | intron-variant | EML5 | GRCh38.p7 | 14:88751918 | AAAAATTTTAGCACA[C/T]CAAATATTTAAATAA | 161436 |
rs10130182 | snp | A/G | 0.49999 | 0.00219646 | intron-variant | EML5 | GRCh38.p7 | 14:88761250 | atacatgtgcagaac[A/G]tgcaggtttgttgca | 161436 |
rs10130222 | snp | A/G | 0.366679 | 0.221102 | intron-variant | EML5 | GRCh38.p7 | 14:88754044 | CAGGAAGGTGAGGCA[A/G]GAACATTGCTTGAGC | 161436 |
rs10131820 | snp | A/G | 0.151668 | 0.229849 | intron-variant | EML5 | GRCh38.p7 | 14:88736798 | ccccacctttcactt[A/G]ctttacacatattta | 161436 |
rs10132009 | snp | C/T | 0.226779 | 0.248919 | intron-variant | EML5 | GRCh38.p7 | 14:88670012 | gaagaggaagagggg[C/T]ctgactgttaaaaga | 161436 |
rs10132509 | snp | A/G | 0.325799 | 0.238232 | intron-variant | EML5 | GRCh38.p7 | 14:88737437 | GGATCCAGCCAGAGT[A/G]TAAGCCAAGCGCAGC | 161436 |
rs10133077 | snp | A/G | 0.163892 | 0.234703 | intron-variant | EML5 | GRCh38.p7 | 14:88667104 | actgagatgggataa[A/G]ctagaggaggaacca | 161436 |
rs10133418 | snp | C/T | 0.307671 | 0.243257 | intron-variant | EML5 | GRCh38.p7 | 14:88723168 | ctgtaatcccagcac[C/T]ttcagcagctgaggc | 161436 |
rs10135487 | snp | A/G | 0.309401 | 0.24284 | intron-variant | EML5 | GRCh38.p7 | 14:88710268 | TGTAGGGTATATGTG[A/G]TTCATATGATCATTC | 161436 |
rs10135957 | snp | A/G | 0.046775 | 0.145601 | intron-variant, upstream-variant-2KB | EML5 | GRCh38.p7 | 14:88768485 | gcgcaatcttggctc[A/G]ctgcaacttccactt | 161436 |
rs10136653 | snp | A/G | 0.499958 | 0.00459246 | intron-variant | EML5 | GRCh38.p7 | 14:88668342 | GGAAGAAGAGATAGC[A/G]CTAGCAAAGGAAACA | 161436 |
rs10137142 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | EML5 | GRCh38.p7 | 14:88629546 | TGTTTATTAAGTATA[C/T]TATATTTTCTCCTAT | 161436 |
rs10137515 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | EML5 | GRCh38.p7 | 14:88686051 | AGTGAGGAAAACAGA[C/T]CCTGTGTTAGGGGCA | 161436 |
rs10138646 | snp | G/T | 0.00795532 | 0.062565 | intron-variant | EML5 | GRCh38.p7 | 14:88650957 | TGTTTTCCATATAAA[G/T]TGCTTTATTTCATAT | 161436 |
rs10140214 | snp | C/T | 0.183568 | 0.241012 | intron-variant | EML5 | GRCh38.p7 | 14:88630395 | GCCAAGTGTATTTTG[C/T]CCTTTAGTCTCTGTA | 161436 |
rs10140309 | snp | C/T | 0.305685 | 0.24372 | intron-variant | EML5 | GRCh38.p7 | 14:88781682 | tcatgatagtgagtt[C/T]ccatgagatctgatg | 161436 |
rs10140896 | snp | C/G | 0.370301 | 0.222129 | intron-variant | EML5 | GRCh38.p7 | 14:88752194 | TGGGCATGATTTCTC[C/G]TTGGATATATAGAAG | 161436 |
rs10141577 | snp | A/G | 0.499958 | 0.00459246 | intron-variant | EML5 | GRCh38.p7 | 14:88722553 | ctcgtttataagtgg[A/G]agctgaacaatgaga | 161436 |
rs10141775 | snp | C/T | 0.408871 | 0.193029 | intron-variant | EML5 | GRCh38.p7 | 14:88790843 | AATAATTACTACGGG[C/T]TTACTTTAGTTTTGT | 161436 |
rs10142212 | snp | C/T | 0.310386 | 0.242597 | intron-variant | EML5 | GRCh38.p7 | 14:88705367 | GAAAACTAATATAGT[C/T]ATACATTGCTTGAGA | 161436 |
rs10143829 | snp | C/T | 0.0501905 | 0.150254 | intron-variant | EML5 | GRCh38.p7 | 14:88719563 | GTGCCTCTGAGGAGT[C/T]TGCTGTTGATAACAC | 161436 |
rs10146011 | snp | A/G | 0.0213716 | 0.101139 | intron-variant, synonymous-codon | EML5 | GRCh38.p7 | 14:88616518 | GAAAAGCTAATTACA[A/G]CTTTTGTAGGATGGT | 161436 |
rs10146045 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | EML5 | GRCh38.p7 | 14:88640988 | GTGGGCCTCTAAAAA[A/G]AGAAGAAGAAGAAGA | 161436 |
rs10147037 | snp | G/T | 0.311614 | 0.242289 | intron-variant | EML5 | GRCh38.p7 | 14:88729565 | cttatttggtttttt[G/T]ttttttgtttttttg | 161436 |
rs10149587 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | EML5 | GRCh38.p7 | 14:88750911 | CACAAGACAAGTATA[C/T]TAAGTGAGGAATAGC | 161436 |
rs10150140 | snp | C/T | 0.046775 | 0.145601 | intron-variant | EML5 | GRCh38.p7 | 14:88689618 | gtacgcctgtggtcc[C/T]agccacttgagaggc | 161436 |
rs10150953 | snp | A/G | 0.305186 | 0.243833 | intron-variant | EML5 | GRCh38.p7 | 14:88717931 | TATAGGACGTAATAC[A/G]TACTATAGGTTAAAG | 161436 |
rs10151451 | snp | A/G | 0.15665 | 0.231917 | intron-variant | EML5 | GRCh38.p7 | 14:88707948 | GAAATTCTAACAAAT[A/G]AAATTCCAAGTTCTA | 161436 |
rs10151985 | snp | A/C | 0.0158469 | 0.0875917 | intron-variant | EML5 | GRCh38.p7 | 14:88648293 | AAAAGCCATTCATAT[A/C]CAAGATAACAATGAT | 161436 |
rs10438034 | snp | A/C | 0.305934 | 0.243663 | intron-variant | EML5 | GRCh38.p7 | 14:88670162 | tctactaaaaaaaaa[A/C]caaaaaaaattagct | 161436 |
rs10438197 | snp | G/T | 0.155656 | 0.231515 | intron-variant | EML5 | GRCh38.p7 | 14:88678656 | ATTTTAAAAAAATCT[G/T]ATCTCTGAATCATTA | 161436 |
rs10438198 | snp | C/T | 0.153332 | 0.230554 | intron-variant | EML5 | GRCh38.p7 | 14:88678738 | CAAATTTCACAGAGA[C/T]AATAAAGGTCAACTA | 161436 |
rs10438199 | snp | C/T | 0.153332 | 0.230554 | intron-variant | EML5 | GRCh38.p7 | 14:88678811 | AGACTTTTTGAACAC[C/T]GGAATATGAACACAg | 161436 |
rs10498617 | snp | G/T | 0.0463947 | 0.145069 | intron-variant | EML5 | GRCh38.p7 | 14:88747974 | TGGAAGTAAAGCACT[G/T]TGAACCCTGAAAGAG | 161436 |
rs10535846 | in-del | -/ACC | 0.499995 | 0.00159744 | intron-variant | EML5 | GRCh38.p7 | 14:88658077 | CAGACTAAAAACAGT[-/ACC]ACTACAATTATTCAA | 161436 |
rs10551487 | in-del | -/TA | | | intron-variant | EML5 | GRCh38.p7 | 14:88696174 | CTTTGAATATATATA[-/TA]TATATATATATTTCC | 161436 |
rs10585294 | in-del | -/CAC | 0 | 0 | intron-variant | EML5 | GRCh38.p7 | 14:88658079 | GACTAAAAACAGTAC[-/CAC]TACAATTATTCAAAC | 161436 |
rs10600813 | in-del | -/TGA | | | intron-variant | EML5 | GRCh38.p7 | 14:88633638 | AGCAGTGCAAACAGA[-/TGA]GTGTCATCTATAGCC | 161436 |
rs10607906 | in-del | -/CACTTT | | | intron-variant | EML5 | GRCh38.p7 | 14:88645057 | TTTTAGACCAAGTTT[-/CACTTT]GTCACCCAGGCTGGA | 161436 |
rs10684533 | in-del | -/TTAT | 0 | 0 | intron-variant | EML5 | GRCh38.p7 | 14:88707271 | TATTTATTTATTTAT[-/TTAT]GGCAGAGACAGGGTC | 161436 |
rs10708422 | in-del | -/A | 0.378372 | 0.214524 | intron-variant | EML5 | GRCh38.p7 | 14:88788899 | ACCCCATCTTTACCG[-/A]AAAAAAAAAAAAAAT | 161436 |
rs11159863 | snp | A/G | 0.381503 | 0.21262 | intron-variant | EML5 | GRCh38.p7 | 14:88642434 | AGCCACAGATAAACA[A/G]CTTTCTTAGCCTTTC | 161436 |
rs11159865 | snp | A/G | 0.390277 | 0.206936 | intron-variant | EML5 | GRCh38.p7 | 14:88716995 | TCTTTTAAGAAGCAG[A/G]AGGAGGCAAAAGCCT | 161436 |
rs11159866 | snp | A/G | 0.366679 | 0.221102 | intron-variant | EML5 | GRCh38.p7 | 14:88724659 | TCTTGTAAAACCTCT[A/G]TAAGTGAGCACTCCA | 161436 |
rs11159868 | snp | C/T | 0.37778 | 0.214877 | intron-variant | EML5 | GRCh38.p7 | 14:88760528 | attaacctatgtatc[C/T]atcctttcaccaata | 161436 |
rs11321542 | in-del | -/T | 0 | 0 | intron-variant | EML5 | GRCh38.p7 | 14:88736004 | AGTATTTTTTCTTTC[-/T]TTTTTTTTTTTTTTT | 161436 |
rs11323385 | in-del | -/A | 0.332106 | 0.236133 | upstream-variant-2KB | EML5 | GRCh38.p7 | 14:88793777 | TGATTTCCGAATAGC[-/A]AAAAAAAAAAAAATT | 161436 |
rs11353201 | in-del | -/A | 0 | 0 | intron-variant | EML5 | GRCh38.p7 | 14:88788913 | GAAAAAAAAAAAAAA[-/A]TAGCCCAGCATCATG | 161436 |
rs11382327 | in-del | -/T | 0.200492 | 0.245049 | intron-variant | EML5 | GRCh38.p7 | 14:88622805 | GAATCTTTTTTTTTT[-/T]AAAAAGGCCCTGATA | 161436 |
rs11424891 | in-del | -/T | 0.499954 | 0.00479211 | intron-variant | EML5 | GRCh38.p7 | 14:88709158 | CTAGATATGGGAATA[-/T]ATAAATATATGAAAA | 161436 |
rs11556106 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | ZC3H14 | GRCh38.p7 | 14:88612626 | GTAACTAAGTATATT[C/T]TCTGTGGATTCTGAG | 161436 |
rs11620661 | snp | G/T | 0.499965 | 0.00419314 | intron-variant | EML5 | GRCh38.p7 | 14:88736187 | TGTATTTTTAGTAGA[G/T]ACGGGGTTTCACTAT | 161436 |
rs11620847 | snp | A/T | 0 | 0 | intron-variant | EML5 | GRCh38.p7 | 14:88635880 | agataatcttttttc[A/T]ccatgtgaggatata | 161436 |
rs11623219 | snp | A/C | | | intron-variant | EML5 | GRCh38.p7 | 14:88738436 | AAAAAAAAATCCCCC[A/C]ATTGCTGACAAATTT | 161436 |
rs11624015 | snp | C/T | 0.152001 | 0.229992 | intron-variant | EML5 | GRCh38.p7 | 14:88735004 | ctagataCAGAACAC[C/T]GTGTGATAACAGTAT | 161436 |
rs11625713 | snp | G/T | | | intron-variant | EML5 | GRCh38.p7 | 14:88645071 | tcactttgtcaccca[G/T]gctggagtgccgtgg | 161436 |
rs11625715 | snp | A/G | 0.0349115 | 0.127424 | intron-variant | EML5 | GRCh38.p7 | 14:88645083 | ccaggctggagtgcc[A/G]tggcacattctcgcc | 161436 |
rs11627906 | snp | A/T | | | intron-variant | EML5 | GRCh38.p7 | 14:88738438 | AAAAAAATCCCCCAA[A/T]TGCTGACAAATTTGG | 161436 |
rs11628445 | snp | G/T | 0.307176 | 0.243374 | intron-variant | EML5 | GRCh38.p7 | 14:88780975 | cacttaatgtttgat[G/T]aaatcatctggtact | 161436 |
rs11628477 | snp | A/T | 0.11228 | 0.208646 | intron-variant | EML5 | GRCh38.p7 | 14:88665089 | CCTTTTATATCACAA[A/T]TGAGGAAACAAAAGC | 161436 |
rs11628848 | snp | A/C | 0.108048 | 0.20579 | intron-variant | EML5 | GRCh38.p7 | 14:88747850 | AAGATGGACTTCTAG[A/C]CATGAAGGAGTATCA | 161436 |
rs11844132 | snp | A/G | 0.0433465 | 0.140692 | intron-variant, upstream-variant-2KB | EML5 | GRCh38.p7 | 14:88766533 | aattttggtcagacc[A/G]gtcgtctgctctcaa | 161436 |
rs11844824 | snp | C/T | | | intron-variant | EML5 | GRCh38.p7 | 14:88631566 | ctgaggtcaggagtt[C/T]gagaccagcctagcc | 161436 |
rs11846241 | snp | C/T | 0.499958 | 0.00459246 | intron-variant | EML5 | GRCh38.p7 | 14:88738010 | ATCTTAGGAAAGCTA[C/T]CGTGTTTTTCAGTTT | 161436 |
rs11846554 | snp | C/T | 0.0894459 | 0.191631 | intron-variant | EML5 | GRCh38.p7 | 14:88697896 | atgtgccaccacacc[C/T]agctaattttttgta | 161436 |
rs11847772 | snp | A/C | 0.0399052 | 0.1355 | intron-variant | EML5 | GRCh38.p7 | 14:88726735 | CATACTTTAGTAAAA[A/C]TATTTTGGTTAAAAT | 161436 |
rs11847829 | snp | C/T | 0.325327 | 0.238382 | intron-variant | EML5 | GRCh38.p7 | 14:88756987 | agctgattctaaaat[C/T]cagaaagactcaaaa | 161436 |
rs11848596 | snp | A/G | 0.00835141 | 0.0640778 | downstream-variant-500B, utr-variant-3-prime | EML5, ZC3H14 | GRCh38.p7 | 14:88614799 | CAAGTTTTTACAAAT[A/G]GAGTTGGGCTCATTC | 161436 |
rs11848879 | snp | C/T | 0.0391387 | 0.134304 | intron-variant | EML5 | GRCh38.p7 | 14:88660806 | GAAGTAAATACCAAT[C/T]TTAAGCAGAAAATCA | 161436 |
rs11849683 | snp | C/T | 0.0399052 | 0.1355 | intron-variant | EML5 | GRCh38.p7 | 14:88733668 | TATGACCTATGCCAT[C/T]TCCCATCCCCCAAAA | 161436 |
rs11849928 | snp | C/T | 0.084728 | 0.187577 | intron-variant | EML5 | GRCh38.p7 | 14:88755289 | GATCACAGCAACAAA[C/T]TGGTAGCCTTTTCCT | 161436 |
rs11850506 | snp | C/T | 0.0240643 | 0.107019 | intron-variant | EML5 | GRCh38.p7 | 14:88737650 | GAGACAGAAGAAATA[C/T]GTAAGTCCTTGATCT | 161436 |
rs11851442 | snp | C/G | 0.0425829 | 0.139564 | intron-variant | EML5 | GRCh38.p7 | 14:88672373 | ggagacaagatacca[C/G]aatctctgggacaca | 161436 |
rs11851569 | snp | A/T | | | intron-variant | EML5 | GRCh38.p7 | 14:88744351 | tttatttttaatttt[A/T]aaaaaaatttGGTCC | 161436 |
rs12323593 | snp | A/G | 0.0154538 | 0.0865337 | utr-variant-3-prime, downstream-variant-500B | ZC3H14, EML5 | GRCh38.p7 | 14:88614167 | AGCAGGCTCAAATGT[A/G]GAGTATTTTTCTTTT | 161436 |
rs12323768 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | EML5 | GRCh38.p7 | 14:88666788 | AAGGATTTTGGTATC[C/T]TGTATGAAATCTGAT | 161436 |
rs12385902 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | EML5 | GRCh38.p7 | 14:88732325 | tattaaatagggaat[C/T]gtttccccatttctt | 161436 |
rs12431548 | snp | C/T | 0.382666 | 0.211895 | intron-variant | EML5 | GRCh38.p7 | 14:88635826 | tatgaggatggagcc[C/T]tcacaatgagattag | 161436 |
rs12434935 | snp | C/T | 0.382279 | 0.212137 | intron-variant | EML5 | GRCh38.p7 | 14:88645449 | TGATAGGTACATTAA[C/T]AACAAAGCCTGGATT | 161436 |
rs12434948 | snp | A/G | 0.0244538 | 0.107838 | intron-variant | EML5 | GRCh38.p7 | 14:88645350 | ATTTCTTTGGTGTAC[A/G]TGTCATAATGTAAAT | 161436 |
rs12434978 | snp | A/G | 0.373598 | 0.21731 | intron-variant | EML5 | GRCh38.p7 | 14:88675518 | agagtagaggggccc[A/G]tggcctggcccacaa | 161436 |
rs12435692 | snp | A/G | 0.3748 | 0.216622 | intron-variant | EML5 | GRCh38.p7 | 14:88623141 | CTACCTCAGCCTCCC[A/G]AGTAGCTAGCATTAC | 161436 |
rs12435720 | snp | A/G | 0.36606 | 0.221428 | intron-variant | EML5 | GRCh38.p7 | 14:88676505 | cctcccacaacatgt[A/G]ggaattcaagatgag | 161436 |
rs12436828 | snp | C/T | 0.375 | 0.216506 | intron-variant | EML5 | GRCh38.p7 | 14:88626063 | GTCTCACTACCTCCT[C/T]CTTCCCTCGAAGTAG | 161436 |
rs12436879 | snp | C/T | 0 | 0 | splice-acceptor-variant | EML5 | GRCh38.p7 | 14:88665490 | AGCAACACCTCCCAC[C/T]TGAAAGAGAAAGAGC | 161436 |
rs12436982 | snp | A/G | 0.376592 | 0.215579 | intron-variant | EML5 | GRCh38.p7 | 14:88689862 | agagcttcatggtga[A/G]agacagtcaataaat | 161436 |
rs12586348 | snp | A/G | 0.377385 | 0.215112 | intron-variant | EML5 | GRCh38.p7 | 14:88643523 | TATATGCAAATTACT[A/G]TGCCATTTTATATAA | 161436 |
rs12587200 | snp | C/G | 0.376394 | 0.215696 | intron-variant | EML5 | GRCh38.p7 | 14:88632060 | CAATAAATTTCACTC[C/G]TTATATCTGTGGATA | 161436 |
rs12587531 | snp | A/T | 0.421684 | 0.181726 | intron-variant | EML5 | GRCh38.p7 | 14:88620427 | GTTTTCCAGGGTGAC[A/T]ACTTTTGAAGGGCAG | 161436 |
rs12587598 | snp | C/T | 0.432063 | 0.171327 | intron-variant | EML5 | GRCh38.p7 | 14:88729474 | tgttttaataaaatt[C/T]tgaaacacaagaaaa | 161436 |
rs12587776 | snp | A/G | 0.269267 | 0.249256 | intron-variant | EML5 | GRCh38.p7 | 14:88668299 | AGTCCGGGGAGAAGC[A/G]CTGGAGCAGTCCTAA | 161436 |
rs12588400 | snp | C/T | 0.3744 | 0.216852 | intron-variant | EML5 | GRCh38.p7 | 14:88630008 | TTGCCTTTGATGCAG[C/T]ATAATAAAAACTGTA | 161436 |
rs12588535 | snp | C/G | 0.375 | 0.216506 | intron-variant | EML5 | GRCh38.p7 | 14:88781900 | ttagcagtgtcagaa[C/G]gaactaattcaGTAA | 161436 |
rs12589481 | snp | A/G | 0.371785 | 0.218331 | intron-variant | EML5 | GRCh38.p7 | 14:88682866 | ctctccccttaccaa[A/G]tactcagggcctaaa | 161436 |
rs12589789 | snp | A/G | 0.3744 | 0.216852 | intron-variant | EML5 | GRCh38.p7 | 14:88633874 | ccttggccttccaaa[A/G]cactgggattacagg | 161436 |
rs12589928 | snp | C/T | 0.308166 | 0.243139 | intron-variant | EML5 | GRCh38.p7 | 14:88720613 | caataaactagatat[C/T]gaaggaacatccccc | 161436 |
rs12589982 | snp | A/G | 0.378568 | 0.214407 | intron-variant | EML5 | GRCh38.p7 | 14:88716861 | TGACCACTCTCTCAC[A/G]TGAAGAGTTTCTCTG | 161436 |
rs12590101 | snp | C/G | 0.3746 | 0.216737 | intron-variant | EML5 | GRCh38.p7 | 14:88629506 | AAATTTTCAGGACCT[C/G]TCGAAGTTACTAAAG | 161436 |
rs12590826 | snp | G/T | 0.384401 | 0.210799 | intron-variant | EML5 | GRCh38.p7 | 14:88769357 | gccttgcctcccctt[G/T]gccttctgccatgac | 161436 |
rs12878272 | snp | A/C | 0.157311 | 0.232183 | intron-variant | EML5 | GRCh38.p7 | 14:88695626 | TAAGGGAGGGAGAAT[A/C]AAAGTTTCTCAAATC | 161436 |
rs12878963 | snp | A/T | 0.112983 | 0.209108 | intron-variant | EML5 | GRCh38.p7 | 14:88665920 | ctcaaaaaaaaaaaa[A/T]aTATTTGCTAAAAAG | 161436 |
rs12879080 | snp | G/T | | | intron-variant | EML5 | GRCh38.p7 | 14:88745175 | TGTGTGTTTGTGTGT[G/T]TGTGTGTGTGTGTGT | 161436 |
rs12879656 | snp | C/G | 0.375996 | 0.215928 | intron-variant | EML5 | GRCh38.p7 | 14:88731218 | atgttatccctcccc[C/G]ctccccccaccccat | 161436 |
rs12879683 | snp | C/G | | | intron-variant | EML5 | GRCh38.p7 | 14:88666314 | tcactgcaacctccg[C/G]ctcctgggttcaagt | 161436 |
rs12879952 | snp | C/G | | | intron-variant | EML5 | GRCh38.p7 | 14:88674912 | ttcaagtccaaaatc[C/G]agcaggacagtcaga | 161436 |
rs12879961 | snp | C/G | | | intron-variant | EML5 | GRCh38.p7 | 14:88666313 | ctcactgcaacctcc[C/G]cctcctgggttcaag | 161436 |
rs12880096 | snp | C/T | 0.366679 | 0.221102 | intron-variant | EML5 | GRCh38.p7 | 14:88752471 | ATAGCAAAAATGGGA[C/T]ATGAATTAAGTTTGT | 161436 |
rs12880220 | snp | C/G | | | intron-variant | EML5 | GRCh38.p7 | 14:88674902 | acaggccccattcaa[C/G]tccaaaatccagcag | 161436 |
rs12880367 | snp | A/G | | | intron-variant | EML5 | GRCh38.p7 | 14:88674918 | tccaaaatccagcag[A/G]acagtcagatcttaa | 161436 |
rs12881795 | snp | C/T | 0.499958 | 0.00459246 | intron-variant | EML5 | GRCh38.p7 | 14:88684349 | CTAATTTTTTGTATT[C/T]TTAGTAGAGACGGGG | 161436 |
rs12882155 | snp | G/T | 0 | 0 | intron-variant | EML5 | GRCh38.p7 | 14:88631484 | ctcccaaagtgctaa[G/T]attgccgggcacggt | 161436 |
rs12882276 | snp | A/G | 0.499996 | 0.00139776 | intron-variant | EML5 | GRCh38.p7 | 14:88670108 | gatcatgtggtcagg[A/G]gttcaagaccagcct | 161436 |
rs12883219 | snp | A/G | 0.0422008 | 0.138995 | intron-variant | EML5 | GRCh38.p7 | 14:88640551 | tggcatgtagcaaaa[A/G]catgttaaatgttaa | 161436 |
rs12884177 | snp | G/T | 0.499942 | 0.00539106 | intron-variant | EML5 | GRCh38.p7 | 14:88775996 | tccagagaattctcc[G/T]ggatcttgtctaaga | 161436 |
rs12885143 | snp | A/T | | | intron-variant | EML5 | GRCh38.p7 | 14:88762355 | gtctctaataaaaat[A/T]aaaaattagcgggtt | 161436 |
rs12885340 | snp | C/G | | | intron-variant | EML5 | GRCh38.p7 | 14:88770687 | TTCAGGTATCCTTCA[C/G]GTTAACTTAATATCT | 161436 |
rs12885389 | snp | A/G | 0.49995 | 0.00499176 | intron-variant | EML5 | GRCh38.p7 | 14:88712964 | AGGACTTTAGGACCC[A/G]GTCAGTCTTCATTAC | 161436 |
rs12885399 | snp | A/G | | | intron-variant | EML5 | GRCh38.p7 | 14:88725208 | ccatttgggaagatg[A/G]aaaagttctgaagct | 161436 |
rs12885870 | snp | A/G | 0.376989 | 0.215346 | intron-variant, utr-variant-3-prime | EML5 | GRCh38.p7 | 14:88615945 | GTGCTTTCAGGTTAC[A/G]TGTGTAATATTTTTC | 161436 |
rs12886252 | snp | C/T | | | intron-variant | EML5 | GRCh38.p7 | 14:88770643 | CGATTGGTCCAATTT[C/T]CTTAATGAGAATGAA | 161436 |
rs12886450 | snp | G/T | 0.366266 | 0.221319 | intron-variant | EML5 | GRCh38.p7 | 14:88684678 | GGTTTTTCTTTTCAT[G/T]GGTCCTTTATTTTCT | 161436 |
rs12886799 | snp | A/G | 0.363985 | 0.222503 | intron-variant | EML5 | GRCh38.p7 | 14:88684852 | ATTTTTTCTGTATAC[A/G]TTAAAATTTTTTTCT | 161436 |
rs12886944 | snp | A/G/T | 0 | 0 | intron-variant | EML5 | GRCh38.p7 | 14:88725233 | gaagctagagggtgg[A/G/T]gatggttgcacaaca | 161436 |
rs12886948 | snp | G/T | | | intron-variant | EML5 | GRCh38.p7 | 14:88725239 | agagggtggtgatgg[G/T]tgcacaacaatgtga | 161436 |
rs12886978 | snp | G/T | 0 | 0 | intron-variant | EML5 | GRCh38.p7 | 14:88725293 | tacatttaaaaatgg[G/T]tgaaatgtgaagttt | 161436 |
rs12887278 | snp | C/T | 0.365439 | 0.221752 | intron-variant | EML5 | GRCh38.p7 | 14:88713468 | GCACTCACTCACTTG[C/T]TAATTTAtttactta | 161436 |
rs12887482 | snp | G/T | | | intron-variant | EML5 | GRCh38.p7 | 14:88662339 | AACACAAtttttctt[G/T]ttttttttttttttt | 161436 |
rs12887895 | snp | C/T | 0.383632 | 0.211288 | intron-variant | EML5 | GRCh38.p7 | 14:88706563 | ATGCTGACTCAAAAA[C/T]TGAACAAATGAATGA | 161436 |
rs12888022 | snp | C/T | 0.244256 | 0.249934 | intron-variant | EML5 | GRCh38.p7 | 14:88684999 | GAAAAAAAAACAAAT[C/T]AGCATTTAAAATTAC | 161436 |
rs12888218 | snp | C/T | 0.366473 | 0.221211 | intron-variant | EML5 | GRCh38.p7 | 14:88734413 | cgggggcaatatttc[C/T]tgaaaggggttaaaa | 161436 |
rs12888343 | snp | G/T | 0.499968 | 0.00399348 | intron-variant | EML5 | GRCh38.p7 | 14:88734423 | atttcttgaaagggg[G/T]taaaaatgaattctt | 161436 |
rs12888461 | snp | C/T | 0.097727 | 0.198275 | intron-variant | EML5 | GRCh38.p7 | 14:88619735 | tcccaggctggagtg[C/T]gatggcgcaacctcc | 161436 |
rs12888530 | snp | A/T | 0 | 0 | intron-variant | EML5 | GRCh38.p7 | 14:88694513 | ATTTACGAATATTTT[A/T]CTCCCACTTATCTCT | 161436 |
rs12888683 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EML5 | GRCh38.p7 | 14:88694514 | TTTACGAATATTTTA[C/T]TCCCACTTATCTCTC | 161436 |
rs12888815 | snp | A/T | 0.5 | 0 | intron-variant | EML5 | GRCh38.p7 | 14:88662560 | TTTTTTTTTTTTTTT[A/T]AATACAGGGTCTCAC | 161436 |
rs12888933 | snp | C/T | 0.499946 | 0.00519141 | intron-variant | EML5 | GRCh38.p7 | 14:88701186 | CAAGGGACATCTGGG[C/T]ACTGTCTGGAGACAT | 161436 |
rs12889367 | snp | A/T | | | intron-variant | EML5 | GRCh38.p7 | 14:88650455 | caagactctgtctca[A/T]aagaacaaaacaaaa | 161436 |
rs12889461 | snp | A/G | 0.115438 | 0.210697 | intron-variant | EML5 | GRCh38.p7 | 14:88650282 | acatggtgaaacccc[A/G]tctctactaaaaata | 161436 |
rs12890631 | snp | A/G | | | intron-variant | EML5 | GRCh38.p7 | 14:88747465 | ACCCCACCCACACAC[A/G]CAAACACAACAAAAT | 161436 |
rs12891253 | snp | C/G | 0.366679 | 0.221102 | intron-variant | EML5 | GRCh38.p7 | 14:88733143 | AGTGAGGTCTCCACT[C/G]CCACACAAATCTGCA | 161436 |
rs12891429 | snp | A/C | 0.113685 | 0.209567 | intron-variant | EML5 | GRCh38.p7 | 14:88646833 | AGGAAAAAAATGTGC[A/C]AAACTGTGAAGAGAG | 161436 |
rs12892032 | snp | C/T | 0.153332 | 0.230554 | intron-variant | EML5 | GRCh38.p7 | 14:88698203 | TTTTATATAAAAACT[C/T]CTACAGAATTTGATG | 161436 |
rs12892420 | snp | C/T | 0.307176 | 0.243374 | intron-variant | EML5 | GRCh38.p7 | 14:88726038 | TAGAATTCAATTGAA[C/T]TTATCTATCTATAAT | 161436 |
rs12892830 | snp | A/T | 0 | 0 | intron-variant | EML5 | GRCh38.p7 | 14:88694617 | ACAGAAATGGTCAAA[A/T]CTGAACTCCTTTTGG | 161436 |
rs12892845 | snp | A/T | 0 | 0 | intron-variant | EML5 | GRCh38.p7 | 14:88694645 | TGGACAGCATCTATA[A/T]TACCTACTATAGTAC | 161436 |
rs12893262 | snp | C/G | | | intron-variant | EML5 | GRCh38.p7 | 14:88694620 | GAAATGGTCAAAACT[C/G]AACTCCTTTTGGACA | 161436 |
rs12893274 | snp | A/G | 0 | 0 | intron-variant | EML5 | GRCh38.p7 | 14:88694631 | AACTGAACTCCTTTT[A/G]GACAGCATCTATAAT | 161436 |
rs12894209 | snp | G/T | | | intron-variant | EML5 | GRCh38.p7 | 14:88694630 | AAACTGAACTCCTTT[G/T]GGACAGCATCTATAA | 161436 |
rs12894218 | snp | G/T | 0 | 0 | intron-variant | EML5 | GRCh38.p7 | 14:88694646 | GGACAGCATCTATAA[G/T]ACCTACTATAGTACT | 161436 |
rs12894235 | snp | A/T | 0 | 0 | intron-variant | EML5 | GRCh38.p7 | 14:88694682 | ATAGGGAATGCTATT[A/T]GTGGCATGAATGGGT | 161436 |
rs12894733 | snp | C/T | 0.153665 | 0.230694 | intron-variant | EML5 | GRCh38.p7 | 14:88664881 | TGTAGTTTTGATACT[C/T]TGTATTTAACAAAAC | 161436 |
rs12895551 | snp | C/T | 0.499996 | 0.00139776 | intron-variant | EML5 | GRCh38.p7 | 14:88673813 | tacctaggaatatag[C/T]taacaagggaagtga | 161436 |
rs12895772 | snp | C/T | 0.031825 | 0.122064 | intron-variant | EML5 | GRCh38.p7 | 14:88730473 | gcagcttaagaaata[C/T]gtccagagaaaacag | 161436 |
rs12897014 | snp | A/G | 0 | 0 | intron-variant | EML5 | GRCh38.p7 | 14:88699336 | AGAAAGAGATAAAAA[A/G]GGGAGTTGGAGAGTC | 161436 |
rs12897589 | snp | A/G | 0.332337 | 0.236052 | intron-variant | EML5 | GRCh38.p7 | 14:88727598 | agatggggtttctcc[A/G]tgttggtcaggctgg | 161436 |
rs17124812 | snp | C/T | 0.0915702 | 0.193391 | synonymous-codon, nc-transcript-variant | EML5 | GRCh38.p7 | 14:88688280 | ACTTACTTTTTCCAA[C/T]GCATGCATACTGAAC | 161436 |
rs17124821 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | EML5 | GRCh38.p7 | 14:88696015 | GCATGTTTACAGGCT[A/G]TAAAGGCTCAGACCA | 161436 |
rs17124827 | snp | C/T | 0.190519 | 0.242821 | intron-variant | EML5 | GRCh38.p7 | 14:88701083 | TTTCTTCGATTCTAC[C/T]GGGCAAAATTAATCA | 161436 |
rs17124833 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | EML5 | GRCh38.p7 | 14:88707496 | ATACAGATATTCTTA[C/T]TAAAATACACAGGAT | 161436 |
rs17188046 | snp | A/T | 0.382279 | 0.212137 | intron-variant | EML5 | GRCh38.p7 | 14:88624417 | ACTATGTTGGTGACA[A/T]ATCAAATCATAAGTA | 161436 |
rs17188193 | snp | A/G | 0.373598 | 0.21731 | intron-variant | EML5 | GRCh38.p7 | 14:88697712 | AGAGCTGTCAATTAT[A/G]GTTAATTTTGAGACT | 161436 |
rs17188207 | snp | C/G | 0.375598 | 0.21616 | intron-variant | EML5 | GRCh38.p7 | 14:88699579 | GATTACTAGTGAATG[C/G]GAAAAATGGATAGAG | 161436 |
rs17188228 | snp | C/T | 0.453795 | 0.144841 | missense, nc-transcript-variant | EML5 | GRCh38.p7 | 14:88738921 | GATCAATCACAGTAA[C/T]TGGTTTAAAAGTTAA | 161436 |
rs17204115 | snp | A/G | 0.0513262 | 0.151752 | intron-variant | EML5 | GRCh38.p7 | 14:88634910 | AACTAAAGATTTTCC[A/G]TATGCATCTTTTAAT | 161436 |
rs17204164 | snp | A/C | 0.105104 | 0.203734 | synonymous-codon, nc-transcript-variant | EML5 | GRCh38.p7 | 14:88685048 | TGGGCCACTTTTATC[A/C]ACTTCTAGTATTTCA | 161436 |
rs17260338 | snp | A/G | 0.375399 | 0.216275 | intron-variant | EML5 | GRCh38.p7 | 14:88639544 | ATTGAGTCACATTTT[A/G]TATTTGTTCTTATGT | 161436 |
rs17260373 | snp | C/G | 0.376989 | 0.215346 | intron-variant | EML5 | GRCh38.p7 | 14:88662960 | TGTAACTAAACGATA[C/G]AAAGTAGGTATCAGT | 161436 |
rs17260380 | snp | C/T | 0.382085 | 0.212258 | intron-variant | EML5 | GRCh38.p7 | 14:88682142 | ATGATAATAGGATAC[C/T]GAATAGTGAGTAAAT | 161436 |
rs17260408 | snp | A/G | 0.371582 | 0.218444 | intron-variant | EML5 | GRCh38.p7 | 14:88715464 | ATACTAAATTTCTGG[A/G]GTTAATAAAGAATAA | 161436 |
rs17260415 | snp | C/G | 0.37778 | 0.214877 | intron-variant | EML5 | GRCh38.p7 | 14:88745629 | GTAAACCAAACTAAA[C/G]AGACCCTAGGCTCAA | 161436 |
rs17798544 | snp | A/G | 0.0364509 | 0.129988 | intron-variant, downstream-variant-500B | EML5 | GRCh38.p7 | 14:88626721 | ATATGCTTGACCAGG[A/G]CATGTAATGATTAGC | 161436 |
rs28392632 | snp | A/G | 0.138886 | 0.22395 | intron-variant | EML5 | GRCh38.p7 | 14:88690129 | TGAAATCACTAAGTA[A/G]CATCCAGGGAGACAA | 161436 |
rs28399784 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | EML5 | GRCh38.p7 | 14:88692710 | CTAAGGTGCCCAAAT[A/G]AAGTTTGTTTAAGCA | 161436 |
rs28408340 | snp | A/G | 0.366473 | 0.221211 | intron-variant | EML5 | GRCh38.p7 | 14:88780254 | CACCACACCCAGCCC[A/G]TGTTTCTGAAAATTC | 161436 |
rs28411260 | snp | A/C | | | intron-variant | EML5 | GRCh38.p7 | 14:88656309 | AGGATGAGTTCATGT[A/C]CTTTGCAGGGACATG | 161436 |
rs28417859 | snp | C/T | 0.141596 | 0.225274 | intron-variant | EML5 | GRCh38.p7 | 14:88633674 | GTAGCTACTACACAC[C/T]TCTGCCATTGTAGCA | 161436 |
rs28419565 | snp | A/G | 0.141934 | 0.225437 | intron-variant | EML5 | GRCh38.p7 | 14:88631299 | ACACACCGCAGCCTC[A/G]AATTCCTGGGCTCAA | 161436 |
rs28434294 | snp | C/T | 0.030278 | 0.119257 | utr-variant-3-prime, nc-transcript-variant | EML5 | GRCh38.p7 | 14:88615379 | TTCCTTATGGAAATG[C/T]AAGAATAAAATATTT | 161436 |
rs28439299 | snp | C/T | 0.152334 | 0.230133 | intron-variant | EML5 | GRCh38.p7 | 14:88744951 | AACAACTCACCATAA[C/T]ACAGATTATATGAAA | 161436 |
rs28439300 | snp | A/G | 0.14933 | 0.228835 | intron-variant | EML5 | GRCh38.p7 | 14:88739899 | CTTGCTGTTAACAAC[A/G]TGGCAGCTTTGTGCT | 161436 |
rs28439948 | snp | A/G | 0.107694 | 0.205546 | intron-variant | EML5 | GRCh38.p7 | 14:88747213 | GGCCAGGAGATTGAG[A/G]CCAGCCTGGGCAACA | 161436 |
rs28477284 | snp | A/T | 0.180702 | 0.240204 | intron-variant | EML5 | GRCh38.p7 | 14:88700308 | AATTTCTTTTTTTTT[A/T]AATTGTTTTATTTGG | 161436 |
rs28488196 | snp | A/C | | | intron-variant | EML5 | GRCh38.p7 | 14:88678581 | TATAGTACTAGCTTT[A/C]AAATTTTTGTTAATT | 161436 |
rs28489684 | snp | A/G | 0.3742 | 0.216966 | intron-variant | EML5 | GRCh38.p7 | 14:88618510 | AGTGGGGGAGGAAAG[A/G]GGAGCTGTAGGTCAG | 161436 |
rs28503450 | snp | C/G | 0.0463947 | 0.145069 | intron-variant | EML5 | GRCh38.p7 | 14:88698391 | CTTGTCTCAACTTCC[C/G]AAGTAGCTGGGACTA | 161436 |
rs28573202 | snp | C/T | | | intron-variant | EML5 | GRCh38.p7 | 14:88656311 | GATGAGTTCATGTCC[C/T]TTGCAGGGACATGGA | 161436 |
rs28573731 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | EML5 | GRCh38.p7 | 14:88724224 | AGGCTGCAGTGAGCC[A/G]AGATTGCGCCACTGT | 161436 |
rs28610062 | snp | C/T | 0.031825 | 0.122064 | intron-variant | EML5 | GRCh38.p7 | 14:88618907 | AGTTCTTAAAAGTAA[C/T]GTGTGATAAGGCCTC | 161436 |
rs28633184 | snp | A/G | 0.046775 | 0.145601 | intron-variant | EML5 | GRCh38.p7 | 14:88716890 | TGACAAATTTAAAGC[A/G]AAGACGACAACTATT | 161436 |
rs28708816 | snp | A/G | 0.046775 | 0.145601 | intron-variant | EML5 | GRCh38.p7 | 14:88759032 | ACTGCTAATGAGCTT[A/G]GGAATTTTTTAGGGG | 161436 |
rs28714506 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | EML5 | GRCh38.p7 | 14:88736087 | CGCACTGCAACCTTC[A/G]CCTCCTGGGTTCAAG | 161436 |
rs28715823 | snp | A/G | | | intron-variant | EML5 | GRCh38.p7 | 14:88738581 | TAGCATTCTAATAGT[A/G]AAATACTTTCAAAAT | 161436 |
rs28755396 | snp | C/T | 0.153665 | 0.230694 | intron-variant | EML5 | GRCh38.p7 | 14:88683997 | TAGCAGGCATCCAGA[C/T]TGGACAAGAAGAAGT | 161436 |
rs28770500 | snp | G/T | | | intron-variant | EML5 | GRCh38.p7 | 14:88729883 | TTGTTTTTTTTTTTT[G/T]TTTTTTTAATGTATT | 161436 |
rs28796383 | snp | C/T | 0.152001 | 0.229992 | intron-variant | EML5 | GRCh38.p7 | 14:88756908 | GCAATACTTCTCAAA[C/T]TGATCTACAGAGTCA | 161436 |
rs28813212 | snp | G/T | 0.5 | 0 | intron-variant | EML5 | GRCh38.p7 | 14:88729874 | TCTTGTTTTTTGTTT[G/T]TTTTTTTTGTTTTTT | 161436 |
rs28863545 | snp | A/G | 0.311859 | 0.242226 | intron-variant | EML5 | GRCh38.p7 | 14:88683773 | ATGAAAATGCTCCAC[A/G]AATTTGGAATAAAAG | 161436 |
rs28889405 | snp | C/G | 0.48 | 0.0979796 | intron-variant | EML5 | GRCh38.p7 | 14:88729870 | TCGGTCTTGTTTTTT[C/G]TTTTTTTTTTTTGTT | 161436 |
rs33917170 | in-del | -/T | | | intron-variant | EML5 | GRCh38.p7 | 14:88709159 | TAGATATGGGAATAA[-/T]TAAATATATGAAAAT | 161436 |
rs33958046 | in-del | -/T/TT | 0.498813 | 0.0243321 | intron-variant | EML5 | GRCh38.p7 | 14:88623017 | CCTCTCTCATAATAC[-/T/TT]TTTTTTTTTTTTTTT | 161436 |
rs33988759 | in-del | -/T | | | intron-variant | EML5 | GRCh38.p7 | 14:88713856 | TTTTTTTTTTTTTTT[-/T]GAGACAGCCTCTTAA | 161436 |
rs33999528 | in-del | -/G | | | intron-variant | EML5 | GRCh38.p7 | 14:88659365 | CAGGGACCCGCCACC[-/G]GTGCCCAGCTAATTT | 161436 |
rs34008480 | in-del | -/A/AA | 0 | 0 | intron-variant | EML5 | GRCh38.p7 | 14:88670336 | AAAAAAAAAAAAAAA[-/A/AA]GGAGAAAAAAGAAAA | 161436 |
rs34012612 | in-del | -/C | | | intron-variant | EML5 | GRCh38.p7 | 14:88664972 | AGTAATTGCTACATT[-/C]ACAGTAGGTTTGTAG | 161436 |
rs34036678 | in-del | -/G | | | intron-variant | EML5 | GRCh38.p7 | 14:88784158 | AAAGCAATACTCAAA[-/G]GGGAAGTTTAAAGTT | 161436 |
rs34166136 | in-del | -/GAT | 0.368529 | 0.220116 | intron-variant | EML5 | GRCh38.p7 | 14:88633636 | AAAGCAGTGCAAACA[-/GAT]GAGTGTCATCTATAG | 161436 |
rs34173550 | snp | G/T | 0.376791 | 0.215463 | intron-variant | EML5 | GRCh38.p7 | 14:88666620 | AACCATATATGAAAT[G/T]ATATTTTTATTATTA | 161436 |
rs34191990 | in-del | -/A | | | intron-variant | EML5 | GRCh38.p7 | 14:88647688 | GAGTGAGACCGTCTC[-/A]AAAAAAAAAAAAAAA | 161436 |
rs34195019 | in-del | -/AT | 0.140242 | 0.224618 | intron-variant | EML5 | GRCh38.p7 | 14:88631165 | TATCAGAGACAAAAG[-/AT]ATTCCCATAGTGTCC | 161436 |
rs34195161 | in-del | -/G | | | intron-variant | EML5 | GRCh38.p7 | 14:88650835 | TTGTAGAAATGGGGT[-/G]CTTGCTGTGTTACCC | 161436 |
rs34195511 | in-del | -/A | | | downstream-variant-500B, utr-variant-3-prime | EML5, ZC3H14 | GRCh38.p7 | 14:88614763 | CAGCCCTAATCCACT[-/A]AAAAAAGGAATTCTA | 161436 |
rs34210771 | snp | C/G | 0.307919 | 0.243198 | intron-variant | EML5 | GRCh38.p7 | 14:88684421 | GTGATCCGCCCGCCT[C/G]GGCCTCCCAAAGTGC | 161436 |
rs34222713 | in-del | -/A | | | intron-variant | EML5 | GRCh38.p7 | 14:88688645 | GGTAACACCTTGCAT[-/A]AACTGCATTTAGACC | 161436 |
rs34247778 | in-del | -/A | | | intron-variant | EML5 | GRCh38.p7 | 14:88656752 | TTGAAATGAGGACTG[-/A]CTATGCTTAAAGAAA | 161436 |
rs34372433 | in-del | -/A | | | intron-variant, downstream-variant-500B | EML5 | GRCh38.p7 | 14:88626616 | GTGAGATACTGTGTC[-/A]AAAAAAAAAAAAAAA | 161436 |
rs34372835 | snp | A/G | 0.0352966 | 0.128072 | intron-variant | EML5 | GRCh38.p7 | 14:88759147 | TACATTTTATGTTAT[A/G]TGAATCATATCTCAG | 161436 |
rs34381823 | snp | C/T | 0.309154 | 0.242901 | intron-variant | EML5 | GRCh38.p7 | 14:88756693 | TCTATACACTAGCAA[C/T]GAACAATAAAAAAAT | 161436 |
rs34382180 | in-del | -/G | | | intron-variant | EML5 | GRCh38.p7 | 14:88621604 | TAGGATTTCCAAACT[-/G]GGGGTCAGTGCAGTG | 161436 |
rs34385850 | in-del | -/A | | | intron-variant | EML5 | GRCh38.p7 | 14:88617800 | CATTTTTCATTGGCC[-/A]AAAAAATGGATAGTC | 161436 |
rs34410354 | in-del | -/A | 0.138886 | 0.22395 | intron-variant | EML5 | GRCh38.p7 | 14:88757456 | CAAAGCATTAGTGAC[-/A]AAAAAAAAAGCAGAT | 161436 |
rs34427680 | in-del | -/T | | | intron-variant | EML5 | GRCh38.p7 | 14:88662486 | TGCTATTTCACGCTT[-/T]CTTGTCTTTTAAGGA | 161436 |
rs34440973 | in-del | -/C | | | upstream-variant-2KB | EML5 | GRCh38.p7 | 14:88793572 | AAGTTTATTTTGTAG[-/C]AGGCGGGGGTCTTGC | 161436 |
rs34443018 | in-del | -/AAG | | | intron-variant | EML5 | GRCh38.p7 | 14:88624859 | AAGCATATGAGGAGG[-/AAG]AAGGTCGGAGAGGAC | 161436 |
rs34468045 | in-del | -/T | 0.0346281 | 0.126945 | intron-variant | EML5 | GRCh38.p7 | 14:88758200 | ATATATGTGTATTTA[-/T]TTTTTTTTTGACACA | 161436 |
rs34510187 | snp | C/T | 0 | 0 | intron-variant | EML5 | GRCh38.p7 | 14:88714877 | ACTTACACTCTGCTT[C/T]CAGTAAAACTCTAAA | 161436 |
rs34681320 | in-del | -/C | | | intron-variant | EML5 | GRCh38.p7 | 14:88633126 | GGTCTGAGCCTGCAG[-/C]CCCCCAGATCATGCC | 161436 |
rs34706463 | snp | A/G | 0.374 | 0.217081 | intron-variant | EML5 | GRCh38.p7 | 14:88669815 | CCAACAGGGGTTGCT[A/G]GACACCTTATACAGG | 161436 |
rs34708784 | in-del | -/T | | | intron-variant | EML5 | GRCh38.p7 | 14:88728992 | TTATAGGAAAAATGA[-/T]TTTTTGTATATTGTT | 161436 |
rs34714100 | in-del | -/G | | | intron-variant | EML5 | GRCh38.p7 | 14:88762285 | GAGGCCGAGGCAGGT[-/G]GGATCACCTGAGGTC | 161436 |
rs34720450 | in-del | -/C | | | intron-variant | EML5 | GRCh38.p7 | 14:88619090 | CTTTCTTAGGCCAGG[-/C]CCCAGTGGCTCACAC | 161436 |
rs34731196 | snp | A/T | 0.161267 | 0.233723 | intron-variant | EML5 | GRCh38.p7 | 14:88784367 | AAAGTTGTTTTTTTT[A/T]AAAAAGTTAAACAAG | 161436 |
rs34733866 | in-del | -/C | | | intron-variant | EML5 | GRCh38.p7 | 14:88721140 | ACAAATGAAAATATT[-/C]CCATGCTCCTGGATA | 161436 |
rs34758290 | snp | C/T | 0.115088 | 0.210473 | intron-variant | EML5 | GRCh38.p7 | 14:88771398 | ACTCCTTGAACTCTC[C/T]GCTTGTGTTCTAGGT | 161436 |
rs34762548 | in-del | -/G | | | intron-variant | EML5 | GRCh38.p7 | 14:88730656 | CTCAATTGTTTATTT[-/G]GGGGAGTCAATGCAA | 161436 |
rs34785936 | in-del | -/G | | | intron-variant | EML5 | GRCh38.p7 | 14:88761368 | ACCCCAGCCCCAACA[-/G]GGCCCTGGTATGTGA | 161436 |
rs34793564 | in-del | -/A | | | intron-variant | EML5 | GRCh38.p7 | 14:88781689 | GTGAGTTCCCATGAG[-/A]ATCTGATGATTTTAT | 161436 |
rs34835895 | snp | A/C | 0.108048 | 0.20579 | intron-variant | EML5 | GRCh38.p7 | 14:88717291 | AAGTTCAGCTTGTGA[A/C]GGCCACTGTAGTTGA | 161436 |
rs34864308 | in-del | -/A | | | intron-variant | EML5 | GRCh38.p7 | 14:88682420 | AATTAAAAAAAAAAA[-/A]CGCAAGCATTTAAAG | 161436 |
rs34874335 | snp | G/T | | | intron-variant | EML5 | GRCh38.p7 | 14:88654310 | GATCTTTATTTCTTG[G/T]CTTCTACTAGCTTTT | 161436 |
rs34908976 | in-del | -/ATATAGTTGAATACA | 0.156319 | 0.231784 | intron-variant | EML5 | GRCh38.p7 | 14:88663453 | TATGATGCTCAATTT[-/ATATAGTTGAATACA]ATATAGTTGAATACA | 161436 |
rs34963584 | in-del | -/G | | | intron-variant | EML5 | GRCh38.p7 | 14:88702849 | AATTTTGACCACCTA[-/G]GCTCAAACGATCCTC | 161436 |
rs34995373 | in-del | -/G | | | intron-variant | EML5 | GRCh38.p7 | 14:88656434 | GAACATATGGACACA[-/G]GGGAGGGGAATATCA | 161436 |
rs35010419 | in-del | -/C | | | intron-variant | EML5 | GRCh38.p7 | 14:88782145 | TATGGACAATAAGGT[-/C]CACCCTGAGGTGGTC | 161436 |
rs35015569 | in-del | -/T | 0.5 | 0 | intron-variant | EML5 | GRCh38.p7 | 14:88780573 | TGTTTATAAAAAATC[-/T]TTTTTTTTTTTCTTT | 161436 |
rs35019185 | in-del | -/G | | | intron-variant | EML5 | GRCh38.p7 | 14:88744977 | GAAAAACATATCAAT[-/G]GCAACTTTGAAATAT | 161436 |
rs35039106 | snp | A/C | | | intron-variant | EML5 | GRCh38.p7 | 14:88641012 | AAGAAGAAGAAAAAT[A/C]TAGAGGAGATGGATA | 161436 |
rs35052140 | snp | A/G | 0.303438 | 0.244222 | intron-variant | EML5 | GRCh38.p7 | 14:88679561 | GCCAGCCGTGGTGGC[A/G]CACGCCTGTAGTCCC | 161436 |
rs35071247 | in-del | -/C | | | intron-variant | EML5 | GRCh38.p7 | 14:88730602 | ATTTTGAGTGGTTTT[-/C]CCTTGATTCTTCATG | 161436 |
rs35093358 | snp | C/T | 0.376195 | 0.215812 | intron-variant | EML5 | GRCh38.p7 | 14:88713996 | GTGCATACCACCATG[C/T]CTGGCTAGTTTTTGT | 161436 |
rs35104991 | in-del | -/C | | | intron-variant | EML5 | GRCh38.p7 | 14:88753736 | GAATGATAATTATAT[-/C]CCTTTGTTGTGAACT | 161436 |
rs35213922 | in-del | -/G | | | intron-variant | EML5 | GRCh38.p7 | 14:88700234 | CACAGTTACTGACAA[-/G]GAGGTTATTCTTTGT | 161436 |
rs35255737 | in-del | -/A/AA | 0.0368353 | 0.130617 | intron-variant | EML5 | GRCh38.p7 | 14:88618011 | AACTTTGATTTCCTT[-/A/AA]AAAAAAAAAACTTGA | 161436 |
rs35269875 | snp | C/G | 0.376989 | 0.215346 | intron-variant | EML5 | GRCh38.p7 | 14:88657145 | GCTACAAACACACAC[C/G]ACTAAACCTGGATTA | 161436 |
rs35329174 | in-del | -/A | | | intron-variant | EML5 | GRCh38.p7 | 14:88753686 | AAAATCATTGACTAG[-/A]AAGTAGATGATAATT | 161436 |
rs35329613 | snp | A/G | | | intron-variant | EML5 | GRCh38.p7 | 14:88631788 | AAAAAGAAAAAAACA[A/G]AACAGAAAAACCCAA | 161436 |
rs35337371 | in-del | -/T | | | intron-variant | EML5 | GRCh38.p7 | 14:88639274 | GGAAGGGCCTTCTAG[-/T]ACAGAGGAACACTTT | 161436 |
rs35339793 | in-del | -/G | | | utr-variant-3-prime, nc-transcript-variant | EML5 | GRCh38.p7 | 14:88615307 | GTGTCTGTTTCCTTA[-/G]GGAAAATGTTTGCCT | 161436 |
rs35340406 | in-del | -/T | | | intron-variant | EML5 | GRCh38.p7 | 14:88656754 | TGAAATGAGGACTGC[-/T]ATGCTTAAAGAAAGG | 161436 |
rs35441941 | in-del | -/C | | | intron-variant | EML5 | GRCh38.p7 | 14:88639572 | GTCAGTGGAGGAAGA[-/C]ACTGCAATCTGTTTT | 161436 |
rs35492665 | in-del | -/A | | | intron-variant, frameshift-variant | EML5 | GRCh38.p7 | 14:88680542 | CGATGGTAGCACCCC[-/A]AGACACCTGAAGAGA | 161436 |
rs35541055 | in-del | -/G | | | intron-variant | EML5 | GRCh38.p7 | 14:88707111 | ATGTTGTATCCTTTT[-/G]GGATATGTCATTTCA | 161436 |
rs35595817 | in-del | -/T | 0.461703 | 0.132974 | intron-variant | EML5 | GRCh38.p7 | 14:88728200 | AGACTTTTTTTTTTT[-/T]GTCATTATTCCCTAA | 161436 |
rs35613883 | in-del | -/A | 0.49645 | 0.0419827 | intron-variant | EML5 | GRCh38.p7 | 14:88776718 | CCAAAAAAAAAAAAA[-/A]TTAGCTGGGCATAGT | 161436 |
rs35634830 | in-del | -/A | | | intron-variant | EML5 | GRCh38.p7 | 14:88660282 | GAGAGACGCTGTCTT[-/A]AAAAAAAAAAAAAAA | 161436 |
rs35642901 | in-del | -/G | | | intron-variant | EML5 | GRCh38.p7 | 14:88651892 | ACTATCTAAATTCTT[-/G]GATTTACATTATTTC | 161436 |
rs35657802 | in-del | -/T | | | intron-variant | EML5 | GRCh38.p7 | 14:88692971 | TTCAATTTATTGAGA[-/T]TTTTGATGTCACATT | 161436 |
rs35668609 | in-del | -/C | | | intron-variant | EML5 | GRCh38.p7 | 14:88684044 | CAGATGACATAATGT[-/C]TGTACACAGAAAACC | 161436 |
rs35685702 | in-del | -/C | 0.384401 | 0.210799 | intron-variant | EML5 | GRCh38.p7 | 14:88760480 | ACCATATCTATATTA[-/C]TTTTCCACAAATTGC | 161436 |
rs35724380 | snp | C/T | | | intron-variant | EML5 | GRCh38.p7 | 14:88752983 | ACCCTTCAATCTGTT[C/T]GTGTAACCTGGTTCT | 161436 |
rs35732162 | in-del | -/T | 0.428182 | 0.17536 | intron-variant | EML5 | GRCh38.p7 | 14:88619685 | GAATTTTTTTTTTTT[-/T]GAGACGAAGTCTCGC | 161436 |
rs35736252 | in-del | -/G | | | intron-variant | EML5 | GRCh38.p7 | 14:88692949 | TTACATATTTTCTCT[-/G]GAACAGTTTCAATTT | 161436 |
rs35767733 | in-del | -/A | | | intron-variant | EML5 | GRCh38.p7 | 14:88717358 | CTGCTGAGGGAGAAT[-/A]CATGAAGTGGGGGCC | 161436 |
rs35784584 | in-del | -/T | | | intron-variant | EML5 | GRCh38.p7 | 14:88713840 | TGCAAAGTTTATTTG[-/T]TTTTTTTTTTTTTTT | 161436 |
rs35798663 | in-del | -/C | | | intron-variant | EML5 | GRCh38.p7 | 14:88760435 | TTTCTCCATTGACTT[-/C]CCCCAAGCACTTTTG | 161436 |
rs35822845 | in-del | -/A | 0.487495 | 0.0780784 | utr-variant-3-prime, nc-transcript-variant | ZC3H14 | GRCh38.p7 | 14:88612980 | CCAAATTAAACTGCT[-/A]AAAAAAAAAAAAAAG | 161436 |
rs35867750 | in-del | -/G | | | intron-variant | EML5 | GRCh38.p7 | 14:88777881 | CAGGAGGCTGAGGTA[-/G]GGAGGGTCACCTGAG | 161436 |
rs35893211 | snp | A/T | 0.107694 | 0.205546 | intron-variant | EML5 | GRCh38.p7 | 14:88733713 | TGACAGTAAATGGCA[A/T]GACTGATTAGCATAC | 161436 |
rs35897446 | in-del | -/T | | | intron-variant | EML5 | GRCh38.p7 | 14:88692993 | GTCACATTGATGGAA[-/T]TTTATAAGTATACTA | 161436 |
rs35901267 | in-del | -/A | | | intron-variant | EML5 | GRCh38.p7 | 14:88718862 | CAACCATTTCATGTG[-/A]AAAAATAATGGACGT | 161436 |
rs35920066 | in-del | -/A/AA/AAA | | | intron-variant | EML5 | GRCh38.p7 | 14:88664275 | AAAAAAAAAAAAAAA[-/A/AA/AAA]GAAAAGAAAAAGGAA | 161436 |
rs35953031 | in-del | -/A/AA/AAA | 0.50155 | 0.156762 | intron-variant | EML5 | GRCh38.p7 | 14:88620934 | ACATCTTCTGCATTT[-/A/AA/AAA]AAAAAAAAAAAAAAA | 161436 |
rs35980266 | in-del | -/G | | | intron-variant | EML5 | GRCh38.p7 | 14:88708356 | TATTTATATAACACT[-/G]GAAATGTAATAGTCT | 161436 |
rs35983405 | in-del | -/C | | | intron-variant | EML5 | GRCh38.p7 | 14:88721111 | TATCCTCTTTTATTT[-/C]CCTTGAGCAGTGGTT | 161436 |
rs36017434 | in-del | -/A/AA | 0.376394 | 0.215696 | intron-variant | EML5 | GRCh38.p7 | 14:88724569 | ATAACTAAAAAAAAA[-/A/AA]TCACTACTTTTGAAT | 161436 |
rs36018473 | in-del | -/AG/GA | 0.5 | 0 | intron-variant | EML5 | GRCh38.p7 | 14:88775924 | TTAGGTGGCTCAGAA[-/AG/GA]GAGAGAGAGAGAGAG | 161436 |
rs36057410 | in-del | -/TTTA | 0.475525 | 0.107882 | intron-variant | EML5 | GRCh38.p7 | 14:88707270 | ATAATAGGGATATAT[-/TTTA]TTTATTTATTTATTT | 161436 |
rs36064771 | snp | C/T | 0.372794 | 0.217765 | intron-variant | EML5 | GRCh38.p7 | 14:88703957 | TAATAAACACTTACA[C/T]AGTGCTTATTATGTG | 161436 |
rs36066768 | in-del | -/A | | | intron-variant | EML5 | GRCh38.p7 | 14:88788537 | CCCTTTCACTATGTT[-/A]AAAAAAAAAAAAAGT | 161436 |
rs36101603 | snp | C/T | 0.499984 | 0.00279548 | intron-variant | EML5 | GRCh38.p7 | 14:88776691 | TTCAAGACCAACGTG[C/T]GTAACATGGCAAAAC | 161436 |
rs36103420 | snp | C/T | 0.375 | 0.216506 | intron-variant | EML5 | GRCh38.p7 | 14:88636340 | TTCCATGGAATGTAG[C/T]TGGAGGGTGCCAAAG | 161436 |
rs36122616 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | EML5 | GRCh38.p7 | 14:88633692 | TGCCATTGTAGCACA[A/G]AAGCTGCCACAGAAC | 161436 |
rs36124282 | snp | G/T | 0.370568 | 0.219005 | intron-variant | EML5 | GRCh38.p7 | 14:88729568 | ATTTGGTTTTTTGTT[G/T]TTTGTTTTTTTGAGA | 161436 |
rs45497400 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | EML5 | GRCh38.p7 | 14:88740300 | CCAAACTGACTAGAA[A/G]CAATATACTATATTA | 161436 |
rs45541634 | snp | C/T | 0.00318978 | 0.0398085 | utr-variant-3-prime, nc-transcript-variant | ZC3H14 | GRCh38.p7 | 14:88612433 | AGGAACAGTTCTATA[C/T]AGTGCTCTCATTTAC | 161436 |
rs55670689 | snp | G/T | 0.5 | 0 | intron-variant | EML5 | GRCh38.p7 | 14:88668338 | TGCAGGAAGAAGAGA[G/T]AGCACTAGCAAAGGA | 161436 |
rs55712648 | snp | A/C | | | intron-variant | EML5 | GRCh38.p7 | 14:88667332 | GGAGGTTAACTTTAC[A/C]ATTTTGTGTTAAAAG | 161436 |
rs55721093 | snp | A/G | 0.375 | 0.216506 | intron-variant | EML5 | GRCh38.p7 | 14:88694117 | ATTTGTTGAAACTAA[A/G]AAACCAACATATTTG | 161436 |
rs55765642 | snp | A/G | | | intron-variant | EML5 | GRCh38.p7 | 14:88789500 | TGGCAATCCCAGGTG[A/G]TAATAAAATGGTCAA | 161436 |
rs55813240 | in-del | -/T | | | intron-variant | EML5 | GRCh38.p7 | 14:88703845 | CCAAATTAGACATAT[-/T]GAGGGGAGATGATTA | 161436 |
rs55870351 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | EML5 | GRCh38.p7 | 14:88617296 | GGGATCACAGGCATG[C/T]GCTAACATGCCCGGC | 161436 |
rs55873608 | snp | A/G | | | intron-variant | EML5 | GRCh38.p7 | 14:88789530 | AAGAACCAGTAAGCA[A/G]ATGATAGACTAGTCA | 161436 |
rs55900327 | snp | C/G | 0.0240643 | 0.107019 | intron-variant | EML5 | GRCh38.p7 | 14:88773300 | GGATATCTGTCTTTC[C/G]GTGTTTTCAGCTCAT | 161436 |
rs55902136 | snp | A/T | | | intron-variant | EML5 | GRCh38.p7 | 14:88707275 | TAGGGATATATTTTA[A/T]TTATTTATTTATTTA | 161436 |
rs55918732 | snp | A/G | | | intron-variant | EML5 | GRCh38.p7 | 14:88669065 | ACAGCCCACCTGGGA[A/G]CTGCACAGGACAAGG | 161436 |
rs56118455 | snp | A/G | | | intron-variant | EML5 | GRCh38.p7 | 14:88662454 | AATACTCCAATCTTA[A/G]ATGGCATGTCTTCTA | 161436 |
rs56132944 | snp | A/G | | | intron-variant | EML5 | GRCh38.p7 | 14:88662432 | CCTAAGGACGTGGCA[A/G]ATATGCAATACTCCA | 161436 |
rs56144430 | snp | A/G | 0.380724 | 0.213099 | intron-variant | EML5 | GRCh38.p7 | 14:88622013 | TGTATCCTTTAACCA[A/G]TCCTTCCCTATCCCC | 161436 |
rs56155030 | snp | C/T | | | intron-variant | EML5 | GRCh38.p7 | 14:88789612 | GGCAATCCCAGGTGA[C/T]AATAAAATGGTCAAA | 161436 |
rs56251701 | snp | C/T | 0.376195 | 0.215812 | intron-variant | EML5 | GRCh38.p7 | 14:88661021 | TATAAAGAGTTTATA[C/T]TTATTGTTAATAGTA | 161436 |
rs56347693 | in-del | -/A/T | 0.471673 | 0.115589 | intron-variant | EML5 | GRCh38.p7 | 14:88662560 | AAGTGATTTATTCCT[-/A/T]TTTTTTTTTTTTTTT | 161436 |
rs56377518 | snp | C/T | | | intron-variant | EML5 | GRCh38.p7 | 14:88780529 | TGAGGATCGACAGGT[C/T]TAAAATCCACAGGGC | 161436 |
rs56403904 | snp | A/G | | | intron-variant | EML5 | GRCh38.p7 | 14:88693957 | TTTTTTTTTTTTGTA[A/G]AGACAGGGTCTCACT | 161436 |
rs56671371 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | EML5 | GRCh38.p7 | 14:88743034 | ACATAATAATGAATA[C/T]CACCACTGACTTTAC | 161436 |
rs56765027 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant, upstream-variant-2KB | EML5 | GRCh38.p7 | 14:88766072 | CAATCAATACTCTTG[C/T]GATTTCCTATGCCTG | 161436 |
rs56869813 | in-del | -/ATAT | | | intron-variant | EML5 | GRCh38.p7 | 14:88696185 | TATATATATATATAT[-/ATAT]TTCCCTCTGAACTCT | 161436 |
rs56908326 | snp | C/T | | | synonymous-codon, nc-transcript-variant | EML5 | GRCh38.p7 | 14:88658359 | ATGTGTACTATGGGC[C/T]ACATACCTCTTAAAC | 161436 |
rs56917346 | in-del | -/A | 0.499998 | 0.000998401 | intron-variant | EML5 | GRCh38.p7 | 14:88777247 | GGCAGAAGACTTTAC[-/A]AGTGGAAACCTTACA | 161436 |
rs56938632 | in-del | -/GAAAAA/GAAAAAA | 0 | 0 | intron-variant | EML5 | GRCh38.p7 | 14:88660768 | AGAAAAAAGAAAAAA[-/GAAAAA/GAAAAAA]AAAACTTAATATACA | 161436 |
rs56960439 | snp | A/G | 0.382666 | 0.211895 | intron-variant | EML5 | GRCh38.p7 | 14:88679624 | TTGAACCTGGGAGGC[A/G]GAGGATGCACTGAGC | 161436 |
rs56964022 | in-del | -/CAAATTACCA | | | intron-variant | EML5 | GRCh38.p7 | 14:88765124 | TCTATGCTGATGTCA[-/CAAATTACCA]TAAATTTAGCACCTT | 161436 |
rs57011514 | in-del | -/CAACAA | | | intron-variant | EML5 | GRCh38.p7 | 14:88674287 | AAACAACAACAACAA[-/CAACAA]TAAAAACCCTGAGAC | 161436 |
rs57033078 | snp | A/G | | | intron-variant | EML5 | GRCh38.p7 | 14:88775166 | GGCTTGCTGGCTTCA[A/G]GTAGGATACAGCACA | 161436 |
rs57118463 | snp | C/T | 0.383439 | 0.21141 | intron-variant | EML5 | GRCh38.p7 | 14:88665822 | CTGAGGCGGGAGGAC[C/T]GTTTGAGCCCAGGAG | 161436 |
rs57143395 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EML5 | GRCh38.p7 | 14:88714079 | CTGGGCTCAAGCTGT[C/T]GGTCCACTGTGGCCT | 161436 |
rs57362682 | snp | A/G | | | intron-variant | EML5 | GRCh38.p7 | 14:88630050 | TTTTTTTTTTTTTGA[A/G]ATGGAGTTTCGCTCT | 161436 |
rs57416233 | in-del | -/T | 0.369958 | 0.21934 | intron-variant | EML5 | GRCh38.p7 | 14:88731324 | ACATGCAGTGTTTGG[-/T]TTTTTGTCCTTGCGA | 161436 |
rs57461245 | in-del | -/A | | | intron-variant | EML5 | GRCh38.p7 | 14:88749011 | AAAGAAAAAAAAAAA[-/A]CTGAAGAAATAATAG | 161436 |
rs57807970 | in-del | -/A | | | intron-variant | EML5 | GRCh38.p7 | 14:88647710 | AAAAAAAAAAAAAAA[-/A]GGGTTACTCCATTAA | 161436 |
rs57861940 | in-del | -/TA | 0.307671 | 0.243257 | intron-variant | EML5 | GRCh38.p7 | 14:88689322 | CTGTTTTCCGAAGTT[-/TA]TATACCAATGTACAC | 161436 |
rs57889459 | snp | C/T | 0.37778 | 0.214877 | intron-variant | EML5 | GRCh38.p7 | 14:88770820 | ATCTGAGGGTATATT[C/T]CCATTCTAAAACATT | 161436 |
rs57996765 | in-del | -/T/TT | | | intron-variant, upstream-variant-2KB | EML5 | GRCh38.p7 | 14:88768428 | TGTCTTTTTTTTTTT[-/T/TT]GAGACAGAGTTTCGC | 161436 |
rs58052105 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | EML5 | GRCh38.p7 | 14:88684391 | TAGCCGGGATGGTCT[C/T]GATCTCCTGACCTCG | 161436 |
rs58318441 | in-del | -/T | | | intron-variant | EML5 | GRCh38.p7 | 14:88750118 | AAGTTTAAAATATTT[-/T]ACTATTTCACTTACT | 161436 |
rs58336894 | snp | A/T | 0.0193772 | 0.0965046 | intron-variant | EML5 | GRCh38.p7 | 14:88726472 | ATTCTGTATCGCTGA[A/T]GAGAAAATTACTTAT | 161436 |
rs58345114 | snp | C/T | | | intron-variant | EML5 | GRCh38.p7 | 14:88733778 | AGGTTGAGTCCCCAT[C/T]TTACTTCTTACACTA | 161436 |
rs58382081 | in-del | -/T | | | intron-variant | EML5 | GRCh38.p7 | 14:88630047 | TTTTTTTTTTTTTTT[-/T]GAGATGGAGTTTCGC | 161436 |
rs58417652 | snp | C/T | 0.103438 | 0.202533 | intron-variant, upstream-variant-2KB | EML5 | GRCh38.p7 | 14:88766225 | GAAAAAAGAACAGGA[C/T]AACAGCGATGTTCAG | 161436 |
rs58550317 | snp | C/T | 0.3746 | 0.216737 | intron-variant | EML5 | GRCh38.p7 | 14:88775243 | AAGCGGAGTGAAAAG[C/T]AAATACTTTGTCTTG | 161436 |
rs58625162 | snp | C/G | 0.190519 | 0.242821 | intron-variant | EML5 | GRCh38.p7 | 14:88696774 | CAAGCTTAGGTAACA[C/G]TGACTTAGATTAAAA | 161436 |
rs58655091 | snp | A/G | 0.377582 | 0.214995 | intron-variant | EML5 | GRCh38.p7 | 14:88748567 | CATATACTTTAAAAG[A/G]ATATAATAAAATTAC | 161436 |
rs58676323 | in-del | -/AAAA/AAAAAAA | 0 | 0 | intron-variant | EML5 | GRCh38.p7 | 14:88759704 | AAAAAAAAAAAAAAA[-/AAAA/AAAAAAA]CTGGGGAGAAAAACT | 161436 |
rs58698629 | in-del | -/CTTT/CTTTG | 0 | 0 | intron-variant | EML5 | GRCh38.p7 | 14:88729869 | TCGGTCTTGTTTTTT[-/CTTT/CTTTG]GTTTTTTTTTTTTGT | 161436 |
rs58701181 | in-del | -/AC | | | intron-variant | EML5 | GRCh38.p7 | 14:88716733 | GTCCACTGCTCACCA[-/AC]ACACACACACACACA | 161436 |
rs58984912 | snp | A/T | 0.378372 | 0.214524 | intron-variant | EML5 | GRCh38.p7 | 14:88698172 | CACAGTAGTACCAGT[A/T]ACTTTTAAGTTTTCT | 161436 |
rs59074536 | in-del | -/T | | | intron-variant | EML5 | GRCh38.p7 | 14:88758037 | TTTTTTTTTTTTTTT[-/T]GTAGAGATGGGGTCT | 161436 |
rs59186795 | in-del | -/A | | | intron-variant | EML5 | GRCh38.p7 | 14:88643384 | TATTGGGGAAAAAAA[-/A]CAATAAAAAATAACA | 161436 |
rs59203329 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | EML5 | GRCh38.p7 | 14:88747366 | GCAGAGAGCTGAGGT[C/T]GTTCCACTGCACTCT | 161436 |
rs59592642 | snp | C/T | | | intron-variant | EML5 | GRCh38.p7 | 14:88710512 | AGAAAGAGTATATTT[C/T]TAGTAATACTGCCAA | 161436 |
rs59643856 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | EML5 | GRCh38.p7 | 14:88768102 | GTCATGGTTTCTCAT[C/G]ATTAAAGTGGGGTTA | 161436 |
rs59787851 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | EML5 | GRCh38.p7 | 14:88729626 | TAGTGCTGGCGCAAT[C/T]TTAGTTCACTGCAAC | 161436 |
rs59805799 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | EML5 | GRCh38.p7 | 14:88653408 | CCCAGTTTTTGCCCA[C/T]TGAGTATGATATTGG | 161436 |
rs59827964 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | EML5 | GRCh38.p7 | 14:88761505 | GGTTTCCAGCTTCAT[C/T]GTCCCTGCAAAGGAC | 161436 |
rs59919777 | snp | A/T | 0.0178098 | 0.0926698 | intron-variant | EML5 | GRCh38.p7 | 14:88687910 | ATCTCTACCAAAAAA[A/T]TTTTTAAAAATTAGA | 161436 |
rs60164768 | in-del | -/T/TT | 0 | 0 | intron-variant | EML5 | GRCh38.p7 | 14:88698283 | TTTTTTTTTTTTTTT[-/T/TT]GAGACAAGGTTTCAC | 161436 |
rs60559048 | in-del | -/TTGAG | 0.5 | 0 | intron-variant | EML5 | GRCh38.p7 | 14:88751618 | GTGTGATATTTAGAG[-/TTGAG]AAGCCAGAGCCACTG | 161436 |
rs60577959 | snp | A/G | 0.5 | 0 | intron-variant | EML5 | GRCh38.p7 | 14:88694169 | TCAAGACTTCATTCA[A/G]ATTTCATCAGTTTTT | 161436 |
rs60585264 | in-del | -/A | 0.310878 | 0.242475 | intron-variant, upstream-variant-2KB | EML5 | GRCh38.p7 | 14:88767883 | CTAAAAACCTTATTC[-/A]AAAATTCACCATTTT | 161436 |
rs60683764 | in-del | -/AC | | | intron-variant | EML5 | GRCh38.p7 | 14:88716764 | CACACACACACACAC[-/AC]GGTAGAAGGTAACAG | 161436 |
rs60686704 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | EML5 | GRCh38.p7 | 14:88657830 | TGGTCAAATTATGGA[A/G]GCTGTGTTTAATTTT | 161436 |
rs60736260 | in-del | -/A | 0.369754 | 0.219451 | intron-variant | EML5 | GRCh38.p7 | 14:88773820 | TCACCTGGAGGTGAT[-/A]AAAAACTTATTACTG | 161436 |
rs60829379 | in-del | -/A | 0.363776 | 0.222609 | intron-variant | EML5 | GRCh38.p7 | 14:88687682 | TGGTAACTACCTGAT[-/A]GGATATGGTGATTAT | 161436 |
rs60873933 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | EML5 | GRCh38.p7 | 14:88617579 | TTTGAGACCAGCCTG[G/T]GCAATATTGTGAGAT | 161436 |
rs61035833 | in-del | -/GTTT | 0 | 0 | intron-variant | EML5 | GRCh38.p7 | 14:88760361 | TTTGTTTGTTTGTTT[-/GTTT]TTTGCTGTCTTTATG | 161436 |
rs61173654 | in-del | -/T | 0.38286 | 0.211774 | intron-variant, utr-variant-3-prime, frameshift-variant | EML5 | GRCh38.p7 | 14:88616052 | ATGTTGACTAGCTGA[-/T]TTTCATAAACCAAAG | 161436 |
rs61480480 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | EML5 | GRCh38.p7 | 14:88645847 | GCTGTCAAATCTCAA[A/G]TCTAGCCCCTCTTCT | 161436 |
rs61528440 | in-del | -/A | 0.382473 | 0.212016 | intron-variant | EML5 | GRCh38.p7 | 14:88713392 | GCGAAACTCCGTCTC[-/A]AAAAAAAAAAATACT | 161436 |
rs61619654 | in-del | -/CATT | 0.367503 | 0.220665 | intron-variant | EML5 | GRCh38.p7 | 14:88684529 | ATTTTAGCATACATT[-/CATT]TTTATTTTTTCTTAG | 161436 |
rs61982732 | snp | C/T | 0.306927 | 0.243432 | intron-variant | EML5 | GRCh38.p7 | 14:88771729 | ATAAACTGTATGTCC[C/T]TATTCCCCTCCATTT | 161436 |
rs61982733 | snp | C/T | 0.377385 | 0.215112 | intron-variant | EML5 | GRCh38.p7 | 14:88776244 | CACCATCCAAGAAAA[C/T]ATGACCTAACCAAAG | 161436 |
rs61982734 | snp | A/C | 0.5 | 0 | intron-variant | EML5 | GRCh38.p7 | 14:88776717 | AAAACCCTGTCTCTA[A/C]CAAAAAAAAAAAAAT | 161436 |
rs61982736 | snp | C/T | 0.309154 | 0.242901 | intron-variant | EML5 | GRCh38.p7 | 14:88786077 | AAAAATACTGGCATT[C/T]TGCTTCAGGGCATTT | 161436 |
rs61982737 | snp | A/T | 0.107694 | 0.205546 | intron-variant | EML5 | GRCh38.p7 | 14:88787527 | TAAATGTAAATCTAA[A/T]AATCTGGCTTCTCCC | 161436 |
rs61982738 | snp | C/T | 0.108402 | 0.206034 | intron-variant | EML5 | GRCh38.p7 | 14:88787821 | TTGAAGCACTACTTC[C/T]ACATATTGCACAGTG | 161436 |
rs61982739 | snp | A/G | 0.498709 | 0.0539355 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | EML5 | GRCh38.p7 | 14:88792533 | CCGCCGCTCCCGCTC[A/G]GGCCCGCGGCGGCGA | 161436 |
rs61983297 | snp | C/T | 0.383632 | 0.211288 | intron-variant | EML5 | GRCh38.p7 | 14:88741122 | GAGCCAAGAGTGTAC[C/T]ACTGCACTCCAGCCT | 161436 |
rs61983299 | snp | A/T | | | intron-variant | EML5 | GRCh38.p7 | 14:88750660 | CTGAAAAGAAAGTTT[A/T]ACTATTTAAACTCCA | 161436 |
rs61983300 | snp | A/G | 0.385168 | 0.210309 | intron-variant | EML5 | GRCh38.p7 | 14:88754047 | GAAGGTGAGGCAGGA[A/G]CATTGCTTGAGCCCA | 161436 |
rs61983301 | snp | C/G | 0.151668 | 0.229849 | intron-variant | EML5 | GRCh38.p7 | 14:88754828 | ATTTTTGTTGAGACA[C/G]AGTCTCGTTCTGTCA | 161436 |
rs61983302 | snp | A/G | 0.37778 | 0.214877 | intron-variant | EML5 | GRCh38.p7 | 14:88762022 | TCATATCCTTAGCCC[A/G]CTTTTTGATAGGGTT | 161436 |
rs61983303 | snp | C/T | 0.384401 | 0.210799 | intron-variant | EML5 | GRCh38.p7 | 14:88764459 | TCAATAGTGATATCC[C/T]GATGAATACTGGTAA | 161436 |
rs61983304 | snp | A/C | | | intron-variant, upstream-variant-2KB | EML5 | GRCh38.p7 | 14:88765913 | AGGGACCGGCTGAAG[A/C]CATGGCAGAAGAACA | 161436 |
rs61984733 | snp | A/T | 0.5 | 0 | intron-variant | EML5 | GRCh38.p7 | 14:88620932 | TTAACATCTTCTGCA[A/T]TTAAAAAAAAAAAAA | 161436 |
rs61984735 | snp | C/T | 0.113685 | 0.209567 | intron-variant | EML5 | GRCh38.p7 | 14:88624139 | GGAGTGCAGTGGCAC[C/T]ATCACAGCTCACTAA | 161436 |
rs61984736 | snp | C/T | 0.310386 | 0.242597 | intron-variant, downstream-variant-500B | EML5 | GRCh38.p7 | 14:88626359 | TATTATGGTGGCTCA[C/T]GCCTGTAAACCCAGC | 161436 |
rs61984737 | snp | A/C | 0.382279 | 0.212137 | intron-variant | EML5 | GRCh38.p7 | 14:88637028 | CAATTACTCTATGAT[A/C]TATATGATTTTTAAC | 161436 |
rs61984738 | snp | A/G | 0.0715223 | 0.175059 | intron-variant | EML5 | GRCh38.p7 | 14:88651807 | AGAAATAATGTTTAA[A/G]TATTTACCAGGTATC | 161436 |
rs61984739 | snp | A/G | | | intron-variant | EML5 | GRCh38.p7 | 14:88655607 | ACAGCAATTGCAACA[A/G]AAGCAAAAATTGACA | 161436 |
rs61984740 | snp | A/T | 0.153332 | 0.230554 | intron-variant | EML5 | GRCh38.p7 | 14:88656968 | AGTGTTAACACATAG[A/T]GTTACCATCAATAGG | 161436 |
rs61984741 | snp | G/T | 0.5 | 0 | intron-variant | EML5 | GRCh38.p7 | 14:88656997 | GGGTTTTGTTTTTGT[G/T]GGTATTTTTTTTTGA | 161436 |
rs61984742 | snp | G/T | 0.5 | 0 | intron-variant | EML5 | GRCh38.p7 | 14:88657000 | TTTTGTTTTTGTGGG[G/T]ATTTTTTTTTGAGAC | 161436 |
rs61984743 | snp | A/G | 0.5 | 0 | intron-variant | EML5 | GRCh38.p7 | 14:88662008 | CAGAGCCTACTAATT[A/G]CTGCAGAAAAATTTT | 161436 |
rs61984744 | snp | A/T | | | intron-variant | EML5 | GRCh38.p7 | 14:88662562 | TTTTTTTTTTTTTTA[A/T]TACAGGGTCTCACTT | 161436 |
rs61984746 | snp | C/T | 0.3748 | 0.216622 | intron-variant | EML5 | GRCh38.p7 | 14:88668136 | CTATGGTGGCTACCT[C/T]TAAGGCTTTTTCAGT | 161436 |
rs61984747 | snp | A/C | | | intron-variant | EML5 | GRCh38.p7 | 14:88670769 | AAGAATGTTACAATG[A/C]AACCACAAGTATCAA | 161436 |
rs61984749 | snp | C/T | 0.112631 | 0.208878 | intron-variant | EML5 | GRCh38.p7 | 14:88674904 | AGGCCCCATTCAAGT[C/T]CAAAATCCAGCAGGA | 161436 |
rs61986661 | snp | A/G | 0.5 | 0 | intron-variant | EML5 | GRCh38.p7 | 14:88686309 | AATGCACTCAAAGAC[A/G]AGTTAACGGGTGCAG | 161436 |
rs61986663 | snp | A/G | 0.5 | 0 | intron-variant | EML5 | GRCh38.p7 | 14:88707992 | TGTTATGTTAGGACA[A/G]TTAAAGAGTTATCTC | 161436 |
rs61986664 | snp | A/G | 0.378174 | 0.214642 | intron-variant | EML5 | GRCh38.p7 | 14:88711251 | ATCTCATCTCGAATT[A/G]TAATCCTCATGTGTT | 161436 |
rs61986665 | snp | C/T | 0.378372 | 0.214524 | intron-variant | EML5 | GRCh38.p7 | 14:88711354 | TGAGTTCTCACGAGA[C/T]CTGATGGTTTAAAAG | 161436 |
rs61986667 | snp | C/G | 0.152667 | 0.230274 | intron-variant | EML5 | GRCh38.p7 | 14:88718740 | TCCTGTGAAAGGGAG[C/G]AAAGTAGAAATGTGA | 161436 |
rs61986668 | snp | C/T | 0.103794 | 0.20279 | intron-variant | EML5 | GRCh38.p7 | 14:88723534 | AGATATACTGTATGG[C/T]ACAGTGATTAGAGTT | 161436 |
rs61986669 | snp | A/C | 0.360632 | 0.224189 | intron-variant | EML5 | GRCh38.p7 | 14:88727121 | AACACAATGTTTTGC[A/C]ATCTAATTGAATAAC | 161436 |
rs61986670 | snp | A/G | 0.384209 | 0.210922 | intron-variant | EML5 | GRCh38.p7 | 14:88730875 | ACAGATTATGAAAAC[A/G]TAAGGGGTTTAAAGC | 161436 |
rs61986671 | snp | A/G | 0.378568 | 0.214407 | intron-variant | EML5 | GRCh38.p7 | 14:88732917 | CCAGGTTCTAGCGAT[A/G]TTATTAAACACTGAA | 161436 |
rs66754813 | in-del | -/T | 0.372592 | 0.217879 | intron-variant | EML5 | GRCh38.p7 | 14:88684880 | TCTGTATACATTAAA[-/T]TTTTTTTCTGTATAC | 161436 |
rs66921772 | in-del | -/GT | 0 | 0 | intron-variant | EML5 | GRCh38.p7 | 14:88716761 | CTGTTACCTTCTACC[-/GT]GTGTGTGTGTGTGTG | 161436 |
rs66922480 | in-del | -/A/AA | 0.625 | 0.125 | intron-variant | EML5 | GRCh38.p7 | 14:88623033 | GCGAGACTACATCTT[-/A/AA]AAAAAAAAAAAAAAA | 161436 |
rs67215394 | in-del | -/AAG/GAA | 0.5 | 0 | intron-variant | EML5 | GRCh38.p7 | 14:88624861 | GCATATGAGGAGGAA[-/AAG/GAA]GGTCGGAGAGGACAC | 161436 |
rs67588787 | snp | A/T | 0.389527 | 0.207442 | intron-variant | EML5 | GRCh38.p7 | 14:88710208 | TAATGAAGAAAAAAA[A/T]ATGAAGAGGGGTGGA | 161436 |
rs67617516 | in-del | -/CATT | | | intron-variant | EML5 | GRCh38.p7 | 14:88684530 | GAAATTTTAGCATAC[-/CATT]ATTTTTATTTTTTCT | 161436 |
rs67626385 | in-del | -/T | 0.306927 | 0.243432 | intron-variant | EML5 | GRCh38.p7 | 14:88759176 | TGTCAGTATTTTTTT[-/T]CACTTTTTAAAAACT | 161436 |
rs67812081 | in-del | -/T | 0.375 | 0.216506 | utr-variant-3-prime, nc-transcript-variant | ZC3H14 | GRCh38.p7 | 14:88612994 | AGCAAGTCAATGAAC[-/T]TTTTTTTTTTTTTTA | 161436 |
rs67979903 | in-del | -/GACT | 0.499995 | 0.00159744 | intron-variant | EML5 | GRCh38.p7 | 14:88656747 | AATTTTTGAAATGAG[-/GACT]GACTATGCTTAAAGA | 161436 |
rs68122150 | snp | C/G | 0.388398 | 0.208197 | intron-variant | EML5 | GRCh38.p7 | 14:88725213 | TGGGAAGATGAAAAA[C/G]TTCTGAAGCTAGAGG | 161436 |
rs68127161 | in-del | -/A | | | intron-variant | EML5 | GRCh38.p7 | 14:88687683 | GGTAACTACCTGATG[-/A]GATATGGTGATTATA | 161436 |
rs71127000 | in-del | -/AC | 0 | 0 | intron-variant | EML5 | GRCh38.p7 | 14:88662339 | AAAAAAAAAAAAAAA[-/AC]CAAGAAAAATTGTGT | 161436 |
rs71127002 | in-del | -/A | 0.5 | 0 | intron-variant | EML5 | GRCh38.p7 | 14:88693764 | AAAAAAAAAAAAAAA[-/A]GATGTTAACATTAGT | 161436 |
rs71130003 | in-del | -/AT | 0 | 0 | intron-variant | EML5 | GRCh38.p7 | 14:88696186 | AGAGTTCAGAGGGAA[-/AT]ATATATATATATATA | 161436 |
rs71130004 | in-del | -/A | 0 | 0 | intron-variant | EML5 | GRCh38.p7 | 14:88713620 | AAAAAAAAAAAAAAA[-/A]TGAGCAGGTTGTGGT | 161436 |
rs71130005 | in-del | -/TCACAGC | 0 | 0 | intron-variant | EML5 | GRCh38.p7 | 14:88719332 | AGTACAGTAGCACAA[-/TCACAGC]TCACTGCAGCCTCCA | 161436 |
rs71130007 | in-del | -/AA/CAA/CAAA | 0 | 0 | intron-variant | EML5 | GRCh38.p7 | 14:88727418 | ACGAAACTCCGTCTC[-/AA/CAA/CAAA]AAAAAAAAAAAAAAA | 161436 |
rs71130008 | in-del | -/C | 0 | 0 | intron-variant | EML5 | GRCh38.p7 | 14:88728212 | TTTAGGGAATAATGA[-/C]CAAAAAAAAAAAGTC | 161436 |
rs71130010 | in-del | -/A | 0 | 0 | intron-variant | EML5 | GRCh38.p7 | 14:88729882 | ATACATTAAAAAAAC[-/A]AAAAAAAAAAAACAA | 161436 |
rs71130011 | in-del | -/A | 0 | 0 | intron-variant | EML5 | GRCh38.p7 | 14:88758207 | GTGAAACTCTGTGTC[-/A]AAAAAAAAATAAATA | 161436 |
rs71130014 | in-del | -/GC | 0 | 0 | utr-variant-5-prime, upstream-variant-2KB | EML5 | GRCh38.p7 | 14:88792671 | CCTCCCGCCTGTGGG[-/GC]CTGAGGCGGCGGCGG | 161436 |
rs71301971 | in-del | -/A | 0.5 | 0 | intron-variant | EML5 | GRCh38.p7 | 14:88780584 | ACTCCATCTTAAAAG[-/A]AAAAAAAAAAAGATT | 161436 |
rs71301972 | in-del | -/A | 0.110519 | 0.207473 | intron-variant | EML5 | GRCh38.p7 | 14:88751507 | ACAAACAAAAAAAAA[-/A]CTCTTCCTCTTGACT | 161436 |
rs71425323 | snp | A/C | 0.5 | 0 | intron-variant | EML5 | GRCh38.p7 | 14:88643384 | ATATTGGGGAAAAAA[A/C]CAATAAAAAATAACA | 161436 |
rs71425324 | snp | C/T | 0.5 | 0 | missense, nc-transcript-variant | EML5 | GRCh38.p7 | 14:88658361 | GTGTACTATGGGCCA[C/T]ATACCTCTTAAACTT | 161436 |
rs71425325 | snp | A/C | 0.5 | 0 | intron-variant | EML5 | GRCh38.p7 | 14:88662275 | CTCTCTTCCTAGGCC[A/C]AGATAAAAAATAAAA | 161436 |
rs71425326 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | EML5 | GRCh38.p7 | 14:88678549 | TTCATGAAGGGACAT[A/G]CATTAATTGTACTCA | 161436 |
rs71425327 | snp | A/G | 0.5 | 0 | intron-variant | EML5 | GRCh38.p7 | 14:88694098 | TCTTATATTACCATA[A/G]ACCATTTGTTGAAAC | 161436 |
rs71425329 | snp | A/C | 0.5 | 0 | intron-variant | EML5 | GRCh38.p7 | 14:88762955 | AATACGTTCTTTGAA[A/C]CCAATGAGAACAAAG | 161436 |
rs71456653 | in-del | -/TA | 0.5 | 0 | intron-variant | EML5 | GRCh38.p7 | 14:88631166 | ATCAGAGACAAAAGA[-/TA]TTCCCATAGTGTCCA | 161436 |
rs71456655 | in-del | -/G | 0.5 | 0 | intron-variant | EML5 | GRCh38.p7 | 14:88665551 | AAAGTATGGGCCAGG[-/G]TGTGGTGGCTCATGC | 161436 |
rs71456657 | in-del | -/A | 0.312348 | 0.242101 | intron-variant | EML5 | GRCh38.p7 | 14:88687765 | ACTTTAAAAAAAAAC[-/A]AAAAAAAACACAAAA | 161436 |
rs71456660 | in-del | -/CT | 0.5 | 0 | intron-variant | EML5 | GRCh38.p7 | 14:88779505 | AAATGAGTTGGTTCT[-/CT]GTCATCTTTAGAAGG | 161436 |
rs71637674 | multinucleotide-polymorphism | CA/TG | 0 | 0 | intron-variant | EML5 | GRCh38.p7 | 14:88721347 | AAGCTGGAGGCATCA[CA/TG]CTACCTGACTTCAAA | 161436 |
rs71858605 | in-del | -/AT | 0.490231 | 0.0692021 | intron-variant | EML5 | GRCh38.p7 | 14:88696165 | TTAGCAACTCTTTGA[-/AT]ATATATATATATATA | 161436 |
rs71951368 | in-del | -/TATT | | | intron-variant | EML5 | GRCh38.p7 | 14:88707297 | TTTATTTATTTATTT[-/TATT]ATTTATTTATGGCAG | 161436 |
rs72147146 | in-del | -/GATTAT | | | intron-variant | EML5 | GRCh38.p7 | 14:88695213 | GAAATCATTTACTAT[-/GATTAT]ATTATTTATTCAATG | 161436 |
rs72177625 | in-del | -/AACAAC | 0.084728 | 0.187577 | intron-variant | EML5 | GRCh38.p7 | 14:88733960 | AGCTATATGAAAAAT[-/AACAAC]AACAACAACAAGAAT | 161436 |
rs72697907 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | EML5 | GRCh38.p7 | 14:88644047 | AACCCTGTACAGTGA[A/G]TATATCGCACAGGGT | 161436 |
rs72697913 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EML5 | GRCh38.p7 | 14:88651455 | TCAGCAATGGGTGGA[A/C]ATTTACATTTAAGTG | 161436 |
rs72697919 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | EML5 | GRCh38.p7 | 14:88657937 | GAGGTTTAATAATAT[A/G]AAATTTACCTTAACA | 161436 |
rs72697934 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EML5 | GRCh38.p7 | 14:88740041 | ACGAAAATTTAATTG[C/T]CTCTGGTAAATTAGC | 161436 |
rs72697940 | snp | C/G | | | intron-variant | EML5 | GRCh38.p7 | 14:88751951 | AGATAATAATAGCAT[C/G]TATTCCAAAGGGTTG | 161436 |
rs72697946 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | EML5 | GRCh38.p7 | 14:88759759 | CAAAATCTTCATACA[A/T]TAGAACAGAGGTATT | 161436 |
rs72697947 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | EML5 | GRCh38.p7 | 14:88767302 | GGTCAGTTCTCAAAG[C/T]GCCTGATATGCAGGC | 161436 |
rs72697949 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | EML5 | GRCh38.p7 | 14:88790603 | ATACAAGTGTACCAC[A/G]AGAAGACCTCAAAAT | 161436 |
rs73321658 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | EML5 | GRCh38.p7 | 14:88624584 | CTAAAGCAACAATGT[A/G]CATTCTACTCCTTAG | 161436 |
rs73321660 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | EML5 | GRCh38.p7 | 14:88625317 | TTTGTCAGGACCTTT[C/T]CCTTTCCAAGTCTGT | 161436 |
rs73321683 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | EML5 | GRCh38.p7 | 14:88672135 | ACGTACCCTAAAATC[A/G]ATCACATAATTGAAA | 161436 |
rs73321685 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | EML5 | GRCh38.p7 | 14:88679069 | CCTCTGCTTCCATCA[C/T]CACGCTGCATTCTCC | 161436 |
rs73327323 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | EML5 | GRCh38.p7 | 14:88691652 | AGCCTAGATCTGGAA[G/T]GGGAGGCAAGAAGCC | 161436 |
rs73327325 | snp | A/G | 0.000323952 | 0.0127229 | missense, nc-transcript-variant | EML5 | GRCh38.p7 | 14:88695454 | AAACGTTTCCCATCC[A/G]CTGTGGAAAATTAAT | 161436 |
rs73327328 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | EML5 | GRCh38.p7 | 14:88713334 | GAGGCAGAGGCTGTA[C/G]TGAGCTAAGAACATG | 161436 |
rs73327331 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | EML5 | GRCh38.p7 | 14:88716310 | TCTGTACTTTTTTTT[A/T]AAGTTTCCCTGGTCA | 161436 |
rs73327335 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | EML5 | GRCh38.p7 | 14:88722688 | CATTTATGCCTAGTG[C/T]TCCATTACTGGAACG | 161436 |
rs73327337 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | EML5 | GRCh38.p7 | 14:88735321 | ACAGACAAGGTTTCT[A/G]ATTTCTTTAATATAT | 161436 |
rs73327339 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | EML5 | GRCh38.p7 | 14:88744697 | AGGTGAAATAAAATA[C/T]GAATGAGAAATGTAA | 161436 |
rs73327340 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | EML5 | GRCh38.p7 | 14:88753006 | CTGGTTCTTCCTGGA[C/T]GCTGGACAATCCAGG | 161436 |
rs73327343 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | EML5 | GRCh38.p7 | 14:88756217 | ACATATGAAATCAAC[A/T]AATATGGCATATTAA | 161436 |
rs73327348 | snp | C/T | 0.0256215 | 0.110247 | intron-variant | EML5 | GRCh38.p7 | 14:88779463 | CAAGGGATAATGGCA[C/T]GTCTTTCATTTACAT | 161436 |
rs73327351 | snp | C/T | 0.0700422 | 0.173537 | upstream-variant-2KB | EML5 | GRCh38.p7 | 14:88793514 | GAGTAGTAAGGAGTA[C/T]AGTTGCGTACCACTA | 161436 |
rs73327352 | snp | G/T | 0.0704125 | 0.17392 | upstream-variant-2KB | EML5 | GRCh38.p7 | 14:88793547 | CCCGGCAAATGTTTT[G/T]CTTTGTTTTTAAGTT | 161436 |
rs74075842 | snp | A/G | 0.0501905 | 0.150254 | intron-variant | EML5 | GRCh38.p7 | 14:88632306 | TTGGACTACTATAAC[A/G]GCCACCTAATTTTCC | 161436 |
rs74075843 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | EML5 | GRCh38.p7 | 14:88637019 | CAAACATTTCAATTA[C/T]TCTATGATCTATATG | 161436 |
rs74075860 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant, utr-variant-3-prime | EML5 | GRCh38.p7 | 14:88680515 | CCCAGTTAAATAAAT[G/T]TTCAGTGGTTCTCGA | 161436 |
rs74075865 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | EML5 | GRCh38.p7 | 14:88716872 | TCACATGAAGAGTTT[C/T]TCTGACAAATTTAAA | 161436 |
rs74075866 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | EML5 | GRCh38.p7 | 14:88735083 | CAGATGAAATCAGGG[A/G]AAAAAAAGACAAACT | 161436 |
rs74075867 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | EML5 | GRCh38.p7 | 14:88737350 | CAACCAGACGCCAAC[A/G]CCCAAGGCAGAAGCA | 161436 |
rs74075868 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | EML5 | GRCh38.p7 | 14:88742340 | TGTGACTGAGGAAAT[A/G]AATTTTAAGTTTCAT | 161436 |
rs74075870 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | EML5 | GRCh38.p7 | 14:88749528 | TATGTAAGATTTTTC[C/T]CATTAAAAAAGTTTT | 161436 |
rs74278116 | in-del | -/GTT | | | intron-variant | EML5 | GRCh38.p7 | 14:88727064 | GTTGTTGTTGTTGTT[-/GTT]TTGGTATCCTTTTAG | 161436 |
rs74335777 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | EML5 | GRCh38.p7 | 14:88756537 | CAAAAAGTAAAAGTA[A/G]AGATCTCTATTGGCA | 161436 |
rs74338046 | snp | C/T | | | intron-variant | EML5 | GRCh38.p7 | 14:88651997 | AAGAATGAATAATTT[C/T]TCAAACTCACACAAC | 161436 |
rs74352481 | snp | A/C | | | intron-variant | EML5 | GRCh38.p7 | 14:88762529 | GGAAAAAAAAAGAAA[A/C]TTACAAAGAGATTTA | 161436 |
rs74352823 | snp | A/T | 0.189576 | 0.242588 | intron-variant | EML5 | GRCh38.p7 | 14:88756312 | CAAAACCCAATCCCT[A/T]CATGATAAAAACACA | 161436 |
rs74387195 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | EML5 | GRCh38.p7 | 14:88759313 | TAGCAAATTCTTTAT[C/T]TTCATCTTGTTTTCT | 161436 |
rs74452965 | snp | C/T | 0.103794 | 0.20279 | intron-variant | EML5 | GRCh38.p7 | 14:88657881 | ATAACGAGCTGATAT[C/T]ACTGGTATATTAGAA | 161436 |
rs74471803 | snp | A/G | 0.5 | 0 | intron-variant | EML5 | GRCh38.p7 | 14:88655985 | gatgctggagaagat[A/G]tggagaaacagcaat | 161436 |
rs74494673 | snp | C/T | 0.5 | 0 | upstream-variant-2KB | EML5 | GRCh38.p7 | 14:88793571 | GTGAAACCCGGTCTC[C/T]ACTAAAAATACAAAA | 161436 |
rs74510630 | snp | A/G | 0.5 | 0 | intron-variant | EML5 | GRCh38.p7 | 14:88656555 | AAACCACCATGGCAC[A/G]TGTATACCTATGTAA | 161436 |
rs74545125 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | EML5 | GRCh38.p7 | 14:88693592 | TCAACTACATAAATG[C/T]AGCCAATAAATGGCA | 161436 |
rs74565504 | snp | G/T | 0.0271762 | 0.113356 | intron-variant | EML5 | GRCh38.p7 | 14:88740803 | CTGTAAGAATAAGGG[G/T]TTTGAATCAGATTAT | 161436 |
rs74631832 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | EML5 | GRCh38.p7 | 14:88667337 | TTAACTTTACAATTT[C/T]GTGTTAAAAGAATAT | 161436 |
rs74663509 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | EML5 | GRCh38.p7 | 14:88693291 | GTAATCTATAAGGAA[C/T]GAGGTTTAATTGATT | 161436 |
rs74700403 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EML5 | GRCh38.p7 | 14:88638129 | TTTCAATAAATTTTA[C/T]AAACGTATTGAAGTT | 161436 |
rs74723895 | snp | C/T | 0.5 | 0 | intron-variant | EML5 | GRCh38.p7 | 14:88656216 | AGACTTGGAACCAAC[C/T]CAAATGTCCATCAAT | 161436 |
rs74735585 | snp | C/T | 0.0399052 | 0.1355 | intron-variant | EML5 | GRCh38.p7 | 14:88743053 | CACTGACTTTACAGG[C/T]TTCAAAATCTGAGCT | 161436 |
rs74736944 | snp | C/T | 0.0501905 | 0.150254 | intron-variant | EML5 | GRCh38.p7 | 14:88755984 | CTGCACCACTGCATT[C/T]CAGCCTGGGCTTCTG | 161436 |
rs74740009 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | EML5 | GRCh38.p7 | 14:88690599 | ACTGCAAATTGAAAG[C/T]AGGAACAACTGTTTA | 161436 |
rs74752397 | snp | C/T | 0.190205 | 0.242744 | intron-variant | EML5 | GRCh38.p7 | 14:88713082 | GACTAATTCCCTAAG[C/T]GTCACAACAAATAAA | 161436 |
rs74752431 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | EML5 | GRCh38.p7 | 14:88699834 | TCTAAGAAGGAAACA[C/T]GAAACGATGAACAGG | 161436 |
rs74755567 | snp | A/C | 0.102014 | 0.201495 | intron-variant | EML5 | GRCh38.p7 | 14:88717326 | ACACAAACAAGGGGA[A/C]TTTGGTGTGAACTCA | 161436 |
rs74789590 | snp | G/T | 0.375 | 0.216506 | intron-variant | EML5 | GRCh38.p7 | 14:88745167 | GTCTAAATTGTGTGT[G/T]TGTGTGTGTGTGTGT | 161436 |
rs74793027 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | EML5 | GRCh38.p7 | 14:88701962 | TATCCATATAGAGAG[A/G]TATCAGTTAAGATTT | 161436 |
rs74793307 | snp | C/T | 0.0138649 | 0.0820989 | intron-variant | EML5 | GRCh38.p7 | 14:88684978 | AAATAATCAATTGTA[C/T]GTAAAGAAAAAAAAA | 161436 |
rs74799523 | snp | A/G | 0.0501905 | 0.150254 | intron-variant | EML5 | GRCh38.p7 | 14:88744245 | AAAATCTTATGAGAA[A/G]TAAAGTAAATTTGAA | 161436 |
rs74820426 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant, downstream-variant-500B, utr-variant-3-prime | ZC3H14, EML5 | GRCh38.p7 | 14:88613907 | GCTGGCTGATACAGC[A/G]AGGTGGTCAGCTGAT | 161436 |
rs74842515 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | EML5 | GRCh38.p7 | 14:88656270 | GGCACATAAACACCA[C/T]GGAATACTATGCAGC | 161436 |
rs74859740 | snp | C/T | 0.0700422 | 0.173537 | intron-variant | EML5 | GRCh38.p7 | 14:88787291 | TATGCTCATTGAGCA[C/T]CTGATTGTGTCTAAA | 161436 |
rs74888985 | snp | A/C | 0.0456336 | 0.143994 | intron-variant | EML5 | GRCh38.p7 | 14:88724740 | CTGATCATGAATATT[A/C]ATTATTATTCATAAG | 161436 |
rs74912094 | snp | A/T | | | intron-variant | EML5 | GRCh38.p7 | 14:88790777 | TGAAAGGATTAGGGA[A/T]AAAGACAAGACACTG | 161436 |
rs74921092 | snp | A/G | 0.0418186 | 0.138422 | intron-variant | EML5 | GRCh38.p7 | 14:88727918 | TAGAAGATACCCATT[A/G]TTTGAAAATTAAGAA | 161436 |
rs74952657 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EML5 | GRCh38.p7 | 14:88632179 | CCTCACTATGTCATA[C/T]GCCCATACCCAATTA | 161436 |
rs74962314 | snp | G/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | EML5 | GRCh38.p7 | 14:88768355 | CACCCACTAATTTTA[G/T]CAACTATTGGCGGAT | 161436 |
rs74971823 | snp | G/T | 0 | 0 | intron-variant | EML5 | GRCh38.p7 | 14:88630048 | TTTTTTTTTTTTTTT[G/T]AGATGGAGTTTCGCT | 161436 |
rs75006776 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | EML5 | GRCh38.p7 | 14:88778985 | ATGAAACTTCCATGC[C/T]AAAGCATTTAGATTG | 161436 |
rs75015427 | snp | A/C | 0.0174175 | 0.0916809 | intron-variant | EML5 | GRCh38.p7 | 14:88634307 | GCCCCATTTCCTGTA[A/C]AGCCTGTGGAGCTGT | 161436 |
rs75017802 | snp | A/G | 0 | 0 | intron-variant | EML5 | GRCh38.p7 | 14:88720221 | AGAAGAAAGGGTATC[A/G]GCTCCTCTTTGTACT | 161436 |
rs75032425 | snp | A/T | 0.0107246 | 0.0724382 | intron-variant | EML5 | GRCh38.p7 | 14:88788422 | GCCATACATAGAAGC[A/T]ATGAACAGTTATTAT | 161436 |
rs75064735 | snp | A/C | 0.0391387 | 0.134304 | intron-variant | EML5 | GRCh38.p7 | 14:88661954 | AAGTTTTAATGAAAA[A/C]ATAGTTAAATTATTA | 161436 |
rs75103339 | snp | C/G | 0.0252325 | 0.109451 | intron-variant | EML5 | GRCh38.p7 | 14:88659786 | GTGGAATATTTTCTT[C/G]GGTGTCTGAGTTTTC | 161436 |
rs75105122 | snp | C/G | 0.5 | 0 | intron-variant | EML5 | GRCh38.p7 | 14:88783066 | CCTGGGCAAGACAGA[C/G]TGAGACTCCATGTCA | 161436 |
rs75120200 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | EML5 | GRCh38.p7 | 14:88770984 | AAATCCCACAATTAC[A/G]TATTAAGTTGCTTTA | 161436 |
rs75120471 | snp | G/T | 0.444444 | 0.157135 | intron-variant | EML5 | GRCh38.p7 | 14:88762777 | CATTCTTTTGTATTT[G/T]CTGAGGAGTGTTTTT | 161436 |
rs75160423 | snp | C/T | 0.0501905 | 0.150254 | intron-variant | EML5 | GRCh38.p7 | 14:88741231 | GAAGGTAAGTCATCA[C/T]AGACTAAGAAGAAGA | 161436 |
rs75208132 | snp | G/T | 0.0219509 | 0.102438 | missense, utr-variant-3-prime, nc-transcript-variant | EML5 | GRCh38.p7 | 14:88622642 | CACAATCTGTGGCTT[G/T]TCCTGTCTCAAGCCT | 161436 |
rs75225607 | snp | A/G | 0.0267878 | 0.112589 | intron-variant | EML5 | GRCh38.p7 | 14:88642374 | TAAATGAACATCAAG[A/G]AATAATTTTCTCACC | 161436 |
rs75249181 | snp | A/T | 0.0158469 | 0.0875917 | intron-variant | EML5 | GRCh38.p7 | 14:88773379 | AATAAATCTCCAAAC[A/T]GGGAATATCCAGCGT | 161436 |
rs75261248 | snp | C/T | 0.0494327 | 0.149241 | intron-variant | EML5 | GRCh38.p7 | 14:88689068 | TGTTAGAAAACTCAC[C/T]TTCATAACCACATAG | 161436 |
rs75280970 | snp | A/T | 0 | 0 | intron-variant | EML5 | GRCh38.p7 | 14:88721235 | CCATCAAGCTACCAA[A/T]GACTTTTTTCTCAGA | 161436 |
rs75293940 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | EML5 | GRCh38.p7 | 14:88727796 | GTGTGTGTGTAGACA[C/T]ACATATGTATATATC | 161436 |
rs75331461 | snp | G/T | 0.0244538 | 0.107838 | intron-variant, downstream-variant-500B | EML5 | GRCh38.p7 | 14:88626354 | ATCCTTATTATGGTG[G/T]CTCATGCCTGTAAAC | 161436 |
rs75343730 | snp | A/G | 0.0232847 | 0.105357 | intron-variant | EML5 | GRCh38.p7 | 14:88725652 | CTTTAGAAATAAGAA[A/G]AAAGCACACAATGTG | 161436 |
rs75376844 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | EML5 | GRCh38.p7 | 14:88742563 | AAACCTGAAAATGGA[A/G]CCTTTAGCTTTACTT | 161436 |
rs75387736 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | EML5 | GRCh38.p7 | 14:88722783 | AAAAAAAAATTTGCA[A/G]CCCCTGGCATAAATG | 161436 |
rs75436056 | snp | G/T | 0.5 | 0 | intron-variant | EML5 | GRCh38.p7 | 14:88640599 | ATCTTTCCAACTTTT[G/T]GACATAGGCATTTAG | 161436 |
rs75446523 | snp | C/T | 0.190519 | 0.242821 | intron-variant | EML5 | GRCh38.p7 | 14:88780628 | TCATCCAGGCTGGAG[C/T]GCAGAGGCGCGATCT | 161436 |
rs75487512 | snp | A/C | | | intron-variant | EML5 | GRCh38.p7 | 14:88764373 | TTTGAGGGAATAGTT[A/C]ATTTCATCTCAGTTG | 161436 |
rs75551368 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EML5 | GRCh38.p7 | 14:88730178 | TGTTATTGAATTAGA[C/T]GGCAAAGCATTAGGT | 161436 |
rs75602272 | snp | C/G | 0.0501905 | 0.150254 | intron-variant | EML5 | GRCh38.p7 | 14:88665103 | AATGAGGAAACAAAA[C/G]CTCAGAGAAGCATCC | 161436 |
rs75613865 | snp | G/T | 0.5 | 0 | intron-variant | EML5 | GRCh38.p7 | 14:88736017 | TCTTTTTTTTTTTTT[G/T]TTGAGATGGAGTCTC | 161436 |
rs75626560 | snp | A/G | 0.18989 | 0.242666 | intron-variant | EML5 | GRCh38.p7 | 14:88768875 | ACTTTTTCTGGAAAG[A/G]GCTAGAGAGTAAATG | 161436 |
rs75649586 | snp | A/G | 0 | 0 | intron-variant | EML5 | GRCh38.p7 | 14:88653777 | TGATACCAAAGCCTG[A/G]CGGAGATATTAAAAA | 161436 |
rs75662161 | snp | A/C | 0.5 | 0 | intron-variant | EML5 | GRCh38.p7 | 14:88724276 | AAGACTCCATATCAA[A/C]AAAAAAAAAAAAAAA | 161436 |
rs75714316 | snp | G/T | 0.0399052 | 0.1355 | intron-variant | EML5 | GRCh38.p7 | 14:88749850 | ATACTTCTAAGTAAC[G/T]GAAAGGTCACAGAAG | 161436 |
rs75715026 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | EML5 | GRCh38.p7 | 14:88729976 | GAGATGATACACTCT[C/T]ATCACTTTGGACTGC | 161436 |
rs75719188 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EML5 | GRCh38.p7 | 14:88696511 | ACTCTGGCTATAAAA[C/T]GGTAAGTGAGATCAG | 161436 |
rs75728366 | snp | C/T | 0.0633504 | 0.166319 | intron-variant | EML5 | GRCh38.p7 | 14:88648660 | CTGCACCCGGTCAAT[C/T]AACTATTCTTTATAT | 161436 |
rs75822369 | in-del | -/G | | | intron-variant | EML5 | GRCh38.p7 | 14:88674822 | CTTCCTAGATACAAT[-/G]GGGGTACAGGCATTG | 161436 |
rs75826158 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | EML5 | GRCh38.p7 | 14:88770750 | ATATTGCTGAACATA[C/T]AGTAAAAACTCAACA | 161436 |
rs75828697 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | EML5 | GRCh38.p7 | 14:88742676 | ATCAAACACACTGTC[C/T]ATCAAAGATGAACAA | 161436 |
rs75831961 | snp | C/G | 0.000728484 | 0.0190712 | missense, nc-transcript-variant | EML5 | GRCh38.p7 | 14:88618317 | GACATGCCGTTTATA[C/G]CAGCCACTAGAGACC | 161436 |
rs75863798 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | EML5 | GRCh38.p7 | 14:88723385 | ATGATCTTGCTTATA[C/T]GTGGAATCTAAAAAA | 161436 |
rs75884474 | snp | C/G | 0.0138799 | 0.0821421 | intron-variant | EML5 | GRCh38.p7 | 14:88730684 | CAAAGTGTGAAGTGA[C/G]AAGAATTTGCTTTTA | 161436 |
rs75894753 | snp | C/T | | | intron-variant | EML5 | GRCh38.p7 | 14:88765124 | TCTATGCTGATGTCA[C/T]AAATTACCATAAATT | 161436 |
rs75915381 | snp | A/C | | | intron-variant | EML5 | GRCh38.p7 | 14:88758985 | TAGATTAGTGATTGC[A/C]AGGTGCTGGAAGGAG | 161436 |
rs75936559 | snp | A/G | 0.0283406 | 0.115616 | intron-variant | EML5 | GRCh38.p7 | 14:88623790 | TCACTGGAACAGTTT[A/G]GCAGGCTTCTAGTGA | 161436 |
rs75937581 | snp | C/G | 0.0490535 | 0.14873 | intron-variant | EML5 | GRCh38.p7 | 14:88659540 | TTAATAATTAAGTCA[C/G]GGTGAGGGATCTGTC | 161436 |
rs75971021 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | EML5 | GRCh38.p7 | 14:88790002 | TCACATTTGTGAATA[C/T]TACATCTTCTGCTGT | 161436 |
rs75974467 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | EML5 | GRCh38.p7 | 14:88660953 | CTTAATTTTATAAGT[G/T]TAAGTATTTTCTATT | 161436 |
rs76016613 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | EML5 | GRCh38.p7 | 14:88765361 | TAAAGGGACTGAGGC[C/T]TTCACTCCCCTGCTG | 161436 |
rs76069708 | snp | A/C | 0.5 | 0 | intron-variant, downstream-variant-500B | EML5 | GRCh38.p7 | 14:88679737 | GTGCTATAGTCCCTA[A/C]AAAAAAAAACTTTTT | 161436 |
rs76110574 | snp | A/G | | | intron-variant | EML5 | GRCh38.p7 | 14:88650480 | ACAAAACAAAAAAAT[A/G]AAAACAAAAACATTT | 161436 |
rs76156628 | snp | G/T | 0.5 | 0 | intron-variant | EML5 | GRCh38.p7 | 14:88751534 | TTGTTGGTTTTTTTT[G/T]GATAGTGTTCGAATA | 161436 |
rs76167640 | snp | G/T | 0.5 | 0 | intron-variant | EML5 | GRCh38.p7 | 14:88659253 | TCTCTTTTTTTTTTT[G/T]GATACTGGAATGCAG | 161436 |
rs76170111 | snp | A/C | 0.0244538 | 0.107838 | intron-variant | EML5 | GRCh38.p7 | 14:88724338 | CATATGGAGAATACA[A/C]AGCAAATCAAGAAGA | 161436 |
rs76189157 | snp | G/T | 0.19334 | 0.243495 | intron-variant | EML5 | GRCh38.p7 | 14:88746933 | GGCCTAAATTCTCAT[G/T]AAACATGAATCCTTC | 161436 |
rs76211195 | snp | G/T | | | intron-variant | EML5 | GRCh38.p7 | 14:88629274 | TTTAATATGCCACAA[G/T]TTTTAAAGTTTTATT | 161436 |
rs76231557 | snp | G/T | 0.00672037 | 0.0575762 | missense, nc-transcript-variant | EML5 | GRCh38.p7 | 14:88620769 | CTGATATCATGGATT[G/T]CACATCTCCTGTCTC | 161436 |
rs76238189 | snp | A/T | 0.0263992 | 0.111815 | intron-variant | EML5 | GRCh38.p7 | 14:88690067 | CTAGAAGAGTGTTCC[A/T]GGCAGAGGGAGCAGC | 161436 |
rs76240368 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | EML5 | GRCh38.p7 | 14:88787167 | CCTTCTCCCTATTGT[C/T]CTCAAAGACTTAGCT | 161436 |
rs76243347 | snp | C/T | 0.0418186 | 0.138422 | intron-variant | EML5 | GRCh38.p7 | 14:88733203 | CTTTAGCACCATACG[C/T]TGGACTATCCTCCTT | 161436 |
rs76270080 | snp | A/C | 0.5 | 0 | intron-variant | EML5 | GRCh38.p7 | 14:88711943 | GTGAGACCCTGTCTC[A/C]AAAAAAAAAAAAAAA | 161436 |
rs76270673 | snp | C/T | 0.0984431 | 0.198823 | utr-variant-3-prime, nc-transcript-variant | EML5 | GRCh38.p7 | 14:88615385 | ATGGAAATGCAAGAA[C/T]AAAATATTTCATTAA | 161436 |
rs76275250 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EML5 | GRCh38.p7 | 14:88617903 | CATTCCTTTAGATAG[A/G]GAATTAATAACAGTT | 161436 |
rs76275672 | snp | A/C | 0.5 | 0 | intron-variant | EML5 | GRCh38.p7 | 14:88676401 | TGAAATGCCAGACAC[A/C]TGAAACCATCAGAAG | 161436 |
rs76284861 | snp | C/T | 0.5 | 0 | intron-variant | EML5 | GRCh38.p7 | 14:88656286 | GGAATACTATGCAGC[C/T]ATAAAAAAGGATGAG | 161436 |
rs76290342 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | EML5 | GRCh38.p7 | 14:88678388 | GCCATCATGGCACAC[A/G]TTTCCCTATGTGACA | 161436 |
rs76321573 | snp | A/C | 0.5 | 0 | intron-variant, downstream-variant-500B | EML5 | GRCh38.p7 | 14:88679738 | TGCTATAGTCCCTAC[A/C]AAAAAAAACTTTTTC | 161436 |
rs76322603 | snp | A/G | 0.046775 | 0.145601 | intron-variant | EML5 | GRCh38.p7 | 14:88696238 | CAGTCAGAGCAGCAA[A/G]AGCATTAATTCACTG | 161436 |
rs76329351 | snp | A/G | 0.0399052 | 0.1355 | intron-variant | EML5 | GRCh38.p7 | 14:88740249 | GAAATCTTGAAAACA[A/G]ATAGATAATTCAGTT | 161436 |
rs76333092 | snp | A/C | 0.5 | 0 | intron-variant | EML5 | GRCh38.p7 | 14:88776719 | AACCCTGTCTCTACC[A/C]AAAAAAAAAAAATTA | 161436 |
rs76340069 | snp | G/T | 0.169797 | 0.236893 | intron-variant | EML5 | GRCh38.p7 | 14:88690360 | AGGTCAAGGATGAAA[G/T]GAGTTAGAAGGCTAT | 161436 |
rs76349283 | snp | A/C | | | intron-variant | EML5 | GRCh38.p7 | 14:88790776 | TTGAAAGGATTAGGG[A/C]AAAAGACAAGACACT | 161436 |
rs76358234 | snp | C/T | | | intron-variant | EML5 | GRCh38.p7 | 14:88722886 | TGCACATTCTGCACA[C/T]GTACTTTGTAACTTA | 161436 |
rs76366769 | snp | G/T | 0.0456336 | 0.143994 | intron-variant | EML5 | GRCh38.p7 | 14:88710216 | AAAAAAATATGAAGA[G/T]GGGTGGAATGCTTTG | 161436 |
rs76453019 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | EML5 | GRCh38.p7 | 14:88783129 | AAGAAAATGCCTGGA[C/T]GTCCAGGTAGAGGTA | 161436 |
rs76455733 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | EML5 | GRCh38.p7 | 14:88630644 | CAGCACATGGTATTC[C/T]CCTAGTATCTTCTCA | 161436 |
rs76507191 | snp | C/T | 0.046775 | 0.145601 | intron-variant | EML5 | GRCh38.p7 | 14:88791356 | CCCAAGAGCACCACA[C/T]AAACACATTCTCAAT | 161436 |
rs76520341 | snp | A/T | 0.0341408 | 0.126114 | intron-variant | EML5 | GRCh38.p7 | 14:88730949 | AGAAAAAAATAAGAC[A/T]CTCTCGTTTTTTTTA | 161436 |
rs76560678 | snp | A/T | 0.5 | 0 | intron-variant | EML5 | GRCh38.p7 | 14:88620936 | CATCTTCTGCATTTA[A/T]AAAAAAAAAAAAAAA | 161436 |
rs76575263 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | EML5 | GRCh38.p7 | 14:88645848 | CTGTCAAATCTCAAA[C/T]CTAGCCCCTCTTCTC | 161436 |
rs76593307 | snp | G/T | 0.0244538 | 0.107838 | intron-variant | EML5 | GRCh38.p7 | 14:88618497 | AAAAGCTCTGATAAG[G/T]GGGGGAGGAAAGGGG | 161436 |
rs76710197 | snp | A/C | 0.5 | 0 | intron-variant, utr-variant-5-prime | EML5 | GRCh38.p7 | 14:88765699 | TTAGAGTATGGATAT[A/C]TTTGGGGCCAGTCTG | 161436 |
rs76726464 | snp | C/T | 0.00377957 | 0.0433071 | intron-variant | EML5 | GRCh38.p7 | 14:88688227 | AAATGCTCTACACTC[C/T]AGGACAAATTTTGTT | 161436 |
rs76750904 | snp | A/G | 0.0271762 | 0.113356 | intron-variant | EML5 | GRCh38.p7 | 14:88642088 | ATATTGATGGTTAAT[A/G]CCGACAAGAGGTGGT | 161436 |
rs76757307 | snp | G/T | 0.5 | 0 | intron-variant | EML5 | GRCh38.p7 | 14:88727419 | TTTTTTTTTTTTTTT[G/T]AGACGGAGTTTCGTT | 161436 |
rs76797694 | snp | A/G | 0.046775 | 0.145601 | intron-variant | EML5 | GRCh38.p7 | 14:88756449 | GTAAAGGGAAAAAAC[A/G]AGGATGTCAGTTCTT | 161436 |
rs76825804 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | EML5 | GRCh38.p7 | 14:88741063 | AGTTACTCGGGAGGC[A/T]GAGGCACAAGAATCG | 161436 |
rs76830450 | snp | A/G | 0.5 | 0 | intron-variant | EML5 | GRCh38.p7 | 14:88738742 | GAAGAATTTTAATCA[A/G]ATGCATACAGGGTGA | 161436 |
rs76834285 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | EML5 | GRCh38.p7 | 14:88646244 | AAAAGTAAATGTGCT[A/G]TATCTTAAACATCCA | 161436 |
rs76838346 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | EML5 | GRCh38.p7 | 14:88688897 | GTATTGTGAATGTGA[C/T]ACTGATTATTCTCAT | 161436 |
rs76854902 | snp | A/G | 0.0490535 | 0.14873 | intron-variant | EML5 | GRCh38.p7 | 14:88697231 | ATAAATGCTTACTGA[A/G]TATCTATTGTTTGTA | 161436 |
rs76857808 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | EML5 | GRCh38.p7 | 14:88679772 | AAAATGTCCTTGAAG[C/T]CATCAAACAAGAGAT | 161436 |
rs76885326 | snp | A/T | 0.5 | 0 | intron-variant | EML5 | GRCh38.p7 | 14:88744750 | ACTAACATTTAAAAA[A/T]TAATTCATTTATTCT | 161436 |
rs76972202 | snp | A/G | 0.046775 | 0.145601 | intron-variant | EML5 | GRCh38.p7 | 14:88756870 | CATTTCTGGGCTTAG[A/G]GGAATGTAATATTTG | 161436 |
rs76976159 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | EML5 | GRCh38.p7 | 14:88730120 | TATTAATACTGGACT[C/T]AGAATGTTACATTTT | 161436 |
rs77038387 | snp | A/T | 0 | 0 | intron-variant | EML5 | GRCh38.p7 | 14:88776731 | ACCAAAAAAAAAAAA[A/T]TTAGCTGGGCATAGT | 161436 |
rs77066868 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | EML5 | GRCh38.p7 | 14:88712799 | GATTAGTCATAACAG[A/G]GTAAGTTATAAAAAA | 161436 |
rs77078520 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | EML5 | GRCh38.p7 | 14:88764277 | AACACAGTTGAGAAG[C/T]AGTACTTCCTCTTCT | 161436 |
rs77083205 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EML5 | GRCh38.p7 | 14:88689358 | ACGAACAGTGAAAAG[A/G]ATTCCTTGTTTCTCA | 161436 |
rs77100215 | snp | C/T | 0.00953873 | 0.0683987 | downstream-variant-500B, utr-variant-3-prime | EML5, ZC3H14 | GRCh38.p7 | 14:88614574 | CACATTAAAAACTCA[C/T]AGGGTCAATACAGCA | 161436 |
rs77138386 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EML5 | GRCh38.p7 | 14:88671931 | CCTACGAAGAGACAA[A/C]TTAAACTCCCACATA | 161436 |
rs77141644 | snp | C/T | | | intron-variant, upstream-variant-2KB | EML5 | GRCh38.p7 | 14:88768471 | GCTGGAGTGCAATGG[C/T]GCAATCTTGGCTCGC | 161436 |
rs77161874 | snp | C/T | 0.0267878 | 0.112589 | intron-variant | EML5 | GRCh38.p7 | 14:88642002 | GCCCAAATTATTAAA[C/T]AGAAAATTGCCACTG | 161436 |
rs77226675 | snp | C/G | 0.5 | 0 | intron-variant | EML5 | GRCh38.p7 | 14:88682421 | ATTAAAAAAAAAAAA[C/G]GCAAGCATTTAAAGT | 161436 |
rs77230377 | snp | C/G/T | 0.0603519 | 0.16452 | intron-variant | EML5 | GRCh38.p7 | 14:88788245 | CAATTACAATTTTGA[C/G/T]TTGCGTTGAATAAAT | 161436 |
rs77235175 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | EML5 | GRCh38.p7 | 14:88779957 | GTTTCTGAAAAAAAA[A/T]TTTTTTTTTTGAAAT | 161436 |
rs77279826 | snp | A/G | 0 | 0 | intron-variant | EML5 | GRCh38.p7 | 14:88721116 | ACTGCTCAATGAAAT[A/G]AAAGAGGACACAAAC | 161436 |
rs77311488 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | EML5 | GRCh38.p7 | 14:88668270 | TAAAGTGTGAGTGTA[C/T]ATATGAAAAGAAAAG | 161436 |
rs77313425 | snp | G/T | 0.0490535 | 0.14873 | intron-variant | EML5 | GRCh38.p7 | 14:88636703 | ACTAGATAAGACTCA[G/T]GGAGAATATGCTAGC | 161436 |
rs77314422 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EML5 | GRCh38.p7 | 14:88700747 | CCAAATGAGGACAAA[C/T]GTTTCTCAGAAAGTG | 161436 |
rs77331118 | snp | C/T | 0.169435 | 0.236663 | intron-variant | EML5 | GRCh38.p7 | 14:88686308 | AAATGCACTCAAAGA[C/T]GAGTTAACGGGTGCA | 161436 |
rs77333298 | snp | A/T | | | intron-variant | EML5 | GRCh38.p7 | 14:88754934 | CTCAGCCTCCTGAGT[A/T]GCTGGGATTACAGGC | 161436 |
rs77334380 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | EML5 | GRCh38.p7 | 14:88749868 | AAGGTCACAGAAGAA[A/G]TAACAAGAAAAATGT | 161436 |
rs77336257 | snp | C/T | 0.261332 | 0.249743 | intron-variant, utr-variant-5-prime | EML5 | GRCh38.p7 | 14:88792269 | AAACTCCGGGAGCGG[C/T]TTGCAGGGTGACGGC | 161436 |
rs77348153 | snp | A/G | 0.0482946 | 0.147699 | intron-variant | EML5 | GRCh38.p7 | 14:88791249 | TCAAACCAAGGTACC[A/G]TATTTGAAATGCCCA | 161436 |
rs77379840 | snp | C/T | | | intron-variant | EML5 | GRCh38.p7 | 14:88680607 | TACATTAACTGTACT[C/T]ATTATAGTACTAGCT | 161436 |
rs77390055 | snp | A/T | 0.02016 | 0.0983543 | intron-variant, downstream-variant-500B, utr-variant-3-prime | ZC3H14 | GRCh38.p7 | 14:88613550 | TGCCCAGACACATAT[A/T]TAAGAGTTTAATCTT | 161436 |
rs77395384 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | EML5 | GRCh38.p7 | 14:88735510 | AATATAACAAGGTAT[C/T]ATTTTTCACCTTTTG | 161436 |
rs77426015 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | EML5 | GRCh38.p7 | 14:88710437 | TATCTAAAATATATT[A/G]ATACACCAGCTACAT | 161436 |
rs77450375 | snp | C/T | 0.0494327 | 0.149241 | intron-variant | EML5 | GRCh38.p7 | 14:88620123 | TTACTATTTTATATA[C/T]TGAAGTTCTGAGGAA | 161436 |
rs77474488 | snp | C/T | 0 | 0 | intron-variant | EML5 | GRCh38.p7 | 14:88721242 | GCTACCAATGACTTT[C/T]TTCTCAGAATTGGAA | 161436 |
rs77528165 | snp | C/T | 0.296364 | 0.245663 | upstream-variant-2KB | EML5 | GRCh38.p7 | 14:88794249 | GTTATCCAATGTCTA[C/T]TTCCTCAAAGATGCC | 161436 |
rs77548033 | snp | C/G | 0.0193772 | 0.0965046 | intron-variant | EML5 | GRCh38.p7 | 14:88683860 | AACCTTATACTCAAT[C/G]GTGGAAGACTAGATG | 161436 |
rs77559651 | snp | A/T | 0.184203 | 0.241186 | intron-variant | EML5 | GRCh38.p7 | 14:88678645 | ATTATTTCAAAATTT[A/T]AAAAAAATCTGATCT | 161436 |
rs77578311 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | EML5 | GRCh38.p7 | 14:88740720 | CATTCAATGTTCAGA[C/T]TCTCATCCTAGTGCT | 161436 |
rs77616601 | snp | A/C | | | intron-variant | EML5 | GRCh38.p7 | 14:88652002 | TGAATAATTTTTCAA[A/C]CTCACACAACTGGTA | 161436 |
rs77662769 | snp | A/G | 0.170084 | 0.236883 | intron-variant | EML5 | GRCh38.p7 | 14:88734160 | GCAAGAAATGTGGAA[A/G]GTTTACAGAAAGGAT | 161436 |
rs77685058 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | EML5 | GRCh38.p7 | 14:88669391 | GCTCCAGTCTGCCAT[G/T]TCTCCTCTGATGGTG | 161436 |
rs77692136 | snp | A/G | 0.0448719 | 0.142907 | intron-variant | EML5 | GRCh38.p7 | 14:88686634 | CTGGACAACATAGAG[A/G]GACCCTGGCTGCACA | 161436 |
rs77726584 | in-del | -/GTTAGAAGCACCA | | | intron-variant | EML5 | GRCh38.p7 | 14:88728328 | TTGAATAATGCACCA[-/GTTAGAAGCACCA]ATTCCCATGCCATCA | 161436 |
rs77759483 | snp | A/C | 0.046775 | 0.145601 | intron-variant | EML5 | GRCh38.p7 | 14:88756752 | ATCAAGAGGAATAAA[A/C]CATTTAGGAATAAAT | 161436 |
rs77803444 | snp | C/G | | | intron-variant | EML5 | GRCh38.p7 | 14:88618159 | GGAATGGCTCTAACA[C/G]TTCAGAAATAGGATT | 161436 |
rs77815152 | snp | G/T | 0.0248432 | 0.108648 | intron-variant | EML5 | GRCh38.p7 | 14:88669790 | TACCTCCTGACTGGG[G/T]GAGACCACCCCAACA | 161436 |
rs77857787 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | EML5 | GRCh38.p7 | 14:88651208 | GCTTGGACTCTGCCA[C/T]GGGGGCCAACAGACC | 161436 |
rs77904629 | snp | A/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | EML5 | GRCh38.p7 | 14:88768354 | TCACCCACTAATTTT[A/G]GCAACTATTGGCGGA | 161436 |
rs77916006 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | EML5 | GRCh38.p7 | 14:88622816 | GAATCTTTTTTTTTT[A/T]AAAAGGCCCTGATAT | 161436 |
rs77916412 | snp | A/G | 0.046775 | 0.145601 | intron-variant | EML5 | GRCh38.p7 | 14:88695808 | TTAATTAAATTCATC[A/G]TAAGAAATTTACTGT | 161436 |
rs77919270 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | EML5 | GRCh38.p7 | 14:88779686 | CAAGATATTCTAGGC[A/G]CAAACCAGGATCAGC | 161436 |
rs77921110 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | EML5 | GRCh38.p7 | 14:88788250 | ACAATTTTGACTTGC[A/G]TTGAATAAATTAAGT | 161436 |
rs77961525 | snp | A/G | 0.5 | 0 | intron-variant | EML5 | GRCh38.p7 | 14:88670867 | ACTACAAGATTAGAG[A/G]AAAAAAAAAAGGATG | 161436 |
rs78025496 | snp | A/G | 0 | 0 | intron-variant | EML5 | GRCh38.p7 | 14:88728328 | TTGAATAATGCACCA[A/G]TTAGAAGCACCAATT | 161436 |
rs78036404 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | EML5 | GRCh38.p7 | 14:88751721 | AAAAGGCTACAGACT[C/T]CTGAAGAACACTGAT | 161436 |
rs78068036 | snp | C/T | 0.384976 | 0.210431 | intron-variant | EML5 | GRCh38.p7 | 14:88754817 | TTTTAAAAATTATTT[C/T]TGTTGAGACAGAGTC | 161436 |
rs78077739 | snp | A/T | 0.383824 | 0.211166 | intron-variant | EML5 | GRCh38.p7 | 14:88741176 | CAAGAAAAAAAAAAA[A/T]TTTAGGTTAAAAAGT | 161436 |
rs78140629 | snp | C/T | 0.0463947 | 0.145069 | intron-variant, upstream-variant-2KB | EML5 | GRCh38.p7 | 14:88767822 | TAACCATATAGTAAT[C/T]GGGAAGAAGAAGGAA | 161436 |
rs78211623 | snp | A/T | | | intron-variant | EML5 | GRCh38.p7 | 14:88660283 | GAGAGACGCTGTCTT[A/T]AAAAAAAAAAAAAAA | 161436 |
rs78213949 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | EML5 | GRCh38.p7 | 14:88735158 | AACTTTTGAGTATAT[C/T]GTAGTCACTTGGAAG | 161436 |
rs78262829 | snp | A/G | 0.0562307 | 0.157967 | intron-variant | EML5 | GRCh38.p7 | 14:88668434 | GAATAAAGTATTTCA[A/G]AAAAAAAAAAGGGAA | 161436 |
rs78405001 | snp | C/T | 0.264084 | 0.249603 | upstream-variant-2KB | EML5 | GRCh38.p7 | 14:88793865 | TAAATTCAATTGTGA[C/T]CCTGTAGAAAACTCC | 161436 |
rs78451024 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | EML5 | GRCh38.p7 | 14:88634174 | CTCATGAGATCTGCT[C/T]GTTTAAACGTGTAGT | 161436 |
rs78471551 | snp | C/T | 0.5 | 0 | intron-variant | EML5 | GRCh38.p7 | 14:88719674 | CTCTATGATATGAGC[C/T]TTTTTTTTTTTAAAC | 161436 |
rs78480119 | snp | C/T | 0.084364 | 0.187256 | intron-variant | EML5 | GRCh38.p7 | 14:88741580 | ACACAGTGGCAAACG[C/T]CTGTAGTCTCAGCAA | 161436 |
rs78480979 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | EML5 | GRCh38.p7 | 14:88748054 | AGGCAATTTCTAGAC[C/T]ATGGCACAGAAAGGT | 161436 |
rs78507384 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | EML5 | GRCh38.p7 | 14:88716835 | TCGCTCCGTCAATAT[C/T]GTGAATTATATGACC | 161436 |
rs78512546 | snp | A/G | 0.5 | 0 | intron-variant | EML5 | GRCh38.p7 | 14:88656550 | GCAGCAAACCACCAT[A/G]GCACATGTATACCTA | 161436 |
rs78572191 | in-del | -/TT | | | intron-variant | EML5 | GRCh38.p7 | 14:88662370 | TTTTTTTTTTTAAAG[-/TT]AAGCAAAAACAGTAA | 161436 |
rs78611599 | snp | G/T | 0.046775 | 0.145601 | intron-variant | EML5 | GRCh38.p7 | 14:88745611 | ATATGTAACAAATTA[G/T]TGGTAAACCAAACTA | 161436 |
rs78614014 | snp | A/G | 0.0240643 | 0.107019 | intron-variant | EML5 | GRCh38.p7 | 14:88752756 | TCACTCTGGCCCACA[A/G]CCCCAACCCTGTACC | 161436 |
rs78623909 | snp | C/T | | | intron-variant | EML5 | GRCh38.p7 | 14:88618160 | GAATGGCTCTAACAG[C/T]TCAGAAATAGGATTT | 161436 |
rs78636629 | snp | A/T | 0.0998734 | 0.199905 | intron-variant | EML5 | GRCh38.p7 | 14:88637119 | ACAGCAAAGTAACAA[A/T]ACAATTCTCTTTATG | 161436 |
rs78653121 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | EML5 | GRCh38.p7 | 14:88708567 | TGGAATGCTAGACTG[C/T]AATGTAGGAAAGAGT | 161436 |
rs78654654 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | EML5 | GRCh38.p7 | 14:88716511 | AGATTTTTAAGAAAA[A/G]TCTAAGGCACTATTT | 161436 |
rs78698701 | snp | G/T | 0.5 | 0 | intron-variant | EML5 | GRCh38.p7 | 14:88657010 | GTGGGTATTTTTTTT[G/T]GAGACAGGGCCTCAT | 161436 |
rs78739761 | snp | G/T | 0.5 | 0 | intron-variant | EML5 | GRCh38.p7 | 14:88659252 | CTCTCTTTTTTTTTT[G/T]TGATACTGGAATGCA | 161436 |
rs78751991 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | EML5 | GRCh38.p7 | 14:88699099 | GGGCATCTCACTCAG[A/G]GATGAAGGGGAGAAG | 161436 |
rs78770314 | snp | C/T | 0.0456336 | 0.143994 | intron-variant | EML5 | GRCh38.p7 | 14:88708616 | GGCATGAACATGATT[C/T]CAACCCCTATAATGC | 161436 |
rs78802511 | snp | A/G | | | intron-variant | EML5 | GRCh38.p7 | 14:88660769 | AGAAAAAAGAAAAAA[A/G]AAACTTAATATACAT | 161436 |
rs78834251 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | EML5 | GRCh38.p7 | 14:88720175 | ACTAAAAGCTCAGGA[C/G]CAGGTGGATTTATAT | 161436 |
rs78890986 | snp | A/G | | | intron-variant | EML5 | GRCh38.p7 | 14:88790778 | GAAAGGATTAGGGAA[A/G]AAGACAAGACACTGG | 161436 |
rs78926317 | snp | A/G | 0.5 | 0 | intron-variant | EML5 | GRCh38.p7 | 14:88670866 | CACTACAAGATTAGA[A/G]AAAAAAAAAAAGGAT | 161436 |
rs78936643 | snp | C/T | 0.0399052 | 0.1355 | intron-variant | EML5 | GRCh38.p7 | 14:88687803 | AGCAGACCTGGCTGG[C/T]ACCATGGCTCATGCC | 161436 |
rs78946296 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | EML5 | GRCh38.p7 | 14:88742564 | AACCTGAAAATGGAG[C/T]CTTTAGCTTTACTTA | 161436 |
rs78953220 | snp | A/G | 0.18989 | 0.242666 | intron-variant | EML5 | GRCh38.p7 | 14:88770314 | TACTTTTTATAATTC[A/G]TGCTTTTTGTGTTCT | 161436 |
rs78994869 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | EML5 | GRCh38.p7 | 14:88711819 | GAATGGTGGCACATG[C/T]CTGTAATCCCAGTTA | 161436 |
rs79031964 | snp | G/T | 0.5 | 0 | intron-variant | EML5 | GRCh38.p7 | 14:88617162 | TTTCTTTTTTTTTTT[G/T]TGAGACGGAGTTTTC | 161436 |
rs79035499 | snp | A/C | | | intron-variant | EML5 | GRCh38.p7 | 14:88660773 | AAAAGAAAAAAAAAA[A/C]TTAATATACATAAGC | 161436 |
rs79254911 | snp | A/T | 0.00716266 | 0.059414 | intron-variant | EML5 | GRCh38.p7 | 14:88790782 | GGATTAGGGAAAAAG[A/T]CAAGACACTGGGGTA | 161436 |
rs79345673 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | EML5 | GRCh38.p7 | 14:88759728 | AAAAACTATGCAGGT[C/T]CTCATAGTTTAACTA | 161436 |
rs79362934 | snp | A/G | | | intron-variant | EML5 | GRCh38.p7 | 14:88728418 | GCCTACTGTTGACTG[A/G]AAGTCTTATCAATAA | 161436 |
rs79405776 | snp | A/G | 0.0952156 | 0.196321 | intron-variant | EML5 | GRCh38.p7 | 14:88637079 | TAAATGCTGTTTTGT[A/G]TTTTGTGGGTATTAA | 161436 |
rs79412496 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | EML5 | GRCh38.p7 | 14:88765590 | CTAGATAATTCAAGA[G/T]ACTCTCAATATCTTA | 161436 |
rs79433568 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | EML5 | GRCh38.p7 | 14:88688811 | GAATGCCTATATATC[C/T]GCTGACCTACAAAAA | 161436 |
rs79437184 | snp | A/C/G | 0.0146753 | 0.0844654 | intron-variant | EML5 | GRCh38.p7 | 14:88743613 | GTTAAATAACTCATA[A/C/G]CAGGTTAAACAGCTA | 161436 |
rs79455957 | snp | C/G | | | intron-variant | EML5 | GRCh38.p7 | 14:88651999 | GAATGAATAATTTTT[C/G]AAACTCACACAACTG | 161436 |
rs79459002 | snp | A/C | 0.5 | 0 | intron-variant | EML5 | GRCh38.p7 | 14:88682420 | AATTAAAAAAAAAAA[A/C]CGCAAGCATTTAAAG | 161436 |
rs79476413 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EML5 | GRCh38.p7 | 14:88729711 | ATTACAAGCATGTGC[C/T]ACCATTCCCCGGCTT | 161436 |
rs79495531 | snp | A/G | 0.0509478 | 0.151255 | intron-variant | EML5 | GRCh38.p7 | 14:88665648 | CCCGGGCAACATAGC[A/G]AGACCCCATCTCTGC | 161436 |
rs79505220 | snp | C/T | | | intron-variant | EML5 | GRCh38.p7 | 14:88685739 | ACAGATGTGGGCCAC[C/T]ACAGCCGGCCCCCAT | 161436 |
rs79525416 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | EML5 | GRCh38.p7 | 14:88787783 | CACAGGGACATTTTA[C/T]TAAATATGTTTTCTA | 161436 |
rs79529361 | snp | G/T | 0.0456336 | 0.143994 | intron-variant | EML5 | GRCh38.p7 | 14:88661261 | GCCTGGCTAATTTTT[G/T]TCTCTGTTTTGTAGA | 161436 |
rs79542177 | snp | A/T | 0 | 0 | intron-variant | EML5 | GRCh38.p7 | 14:88724126 | ATACAAAAAAAAAAA[A/T]TAGCTTGGCGTGGTG | 161436 |
rs79599172 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | EML5 | GRCh38.p7 | 14:88756090 | GGGTCTAAGATGACT[C/G]GGGTTTCTGGCTTGG | 161436 |
rs79623904 | snp | C/G | 0.5 | 0 | intron-variant | EML5 | GRCh38.p7 | 14:88779600 | CCCATGTAGAAGTCA[C/G]TTCATATTGCCTCCT | 161436 |
rs79629725 | snp | A/G | 0.5 | 0 | intron-variant | EML5 | GRCh38.p7 | 14:88656328 | TGCAGGGACATGGAT[A/G]AAGCTGGAAACCATC | 161436 |
rs79632655 | snp | C/T | 0.0463947 | 0.145069 | intron-variant | EML5 | GRCh38.p7 | 14:88700614 | GCAAACCCATTACTC[C/T]ACTACAACAAGCACC | 161436 |
rs79636250 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | EML5 | GRCh38.p7 | 14:88632746 | TTGTCCACCTGGGGC[A/G]CTGAACACTTGCTTT | 161436 |
rs79701184 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | EML5 | GRCh38.p7 | 14:88683513 | TTACCCTGATATCAA[A/G]GCCAGACAAAGATAT | 161436 |
rs79732079 | snp | A/C | | | intron-variant | EML5 | GRCh38.p7 | 14:88685738 | TACAGATGTGGGCCA[A/C]CACAGCCGGCCCCCA | 161436 |
rs79797316 | in-del | -/TT | | | intron-variant | EML5 | GRCh38.p7 | 14:88769980 | AGTTTTTTTTTTTTT[-/TT]GGTCTTTATCCTTAC | 161436 |
rs79833387 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | EML5 | GRCh38.p7 | 14:88632981 | TGTAACTAGATGCTC[C/T]GGATTCCACCTCATA | 161436 |
rs79854697 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | EML5 | GRCh38.p7 | 14:88748024 | GTCCTGTAATCACCC[A/G]AGCTTCCATCTAGGA | 161436 |
rs79856538 | snp | A/G | 0.101658 | 0.201233 | intron-variant | EML5 | GRCh38.p7 | 14:88773255 | TTCCAGGTTCCCTGT[A/G]AGTGAGCATTTTTCT | 161436 |
rs79892555 | snp | G/T | 0.190205 | 0.242744 | intron-variant | EML5 | GRCh38.p7 | 14:88717482 | AAACAAATAAGGCTG[G/T]GTGTGGTGGCTCACG | 161436 |
rs79930862 | snp | C/T | 0.0763149 | 0.179815 | intron-variant | EML5 | GRCh38.p7 | 14:88772448 | CCATCTAAGATGGCA[C/T]TTTCAAGCCTTTGTA | 161436 |
rs79987917 | snp | C/T | 0.0236746 | 0.106192 | intron-variant | EML5 | GRCh38.p7 | 14:88697217 | CATCAATAAAGATGA[C/T]AAATGCTTACTGAAT | 161436 |
rs80003653 | snp | A/C/T | 0.00993785 | 0.0698258 | intron-variant | EML5 | GRCh38.p7 | 14:88683964 | TTCTAGTCAAGACTA[A/C/T]TGGACAAGAAAAAGA | 161436 |
rs80081769 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | EML5 | GRCh38.p7 | 14:88730112 | AATGTATATATTAAT[A/G]CTGGACTTAGAATGT | 161436 |
rs80146984 | snp | A/G | 0.0715223 | 0.175059 | intron-variant | EML5 | GRCh38.p7 | 14:88647777 | AAAAAACAAATAAAT[A/G]AGAATTCAATATATT | 161436 |
rs80200024 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | EML5 | GRCh38.p7 | 14:88717083 | ATCAGAGCATACAAC[C/T]GAAGAATCATTTCTA | 161436 |
rs80201682 | snp | C/G | 0.0193772 | 0.0965046 | intron-variant | EML5 | GRCh38.p7 | 14:88747976 | GAAGTAAAGCACTGT[C/G]AACCCTGAAAGAGGG | 161436 |
rs80205517 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | EML5 | GRCh38.p7 | 14:88772445 | GAACCATCTAAGATG[A/G]CACTTTCAAGCCTTT | 161436 |
rs80211936 | snp | G/T | 0.5 | 0 | intron-variant | EML5 | GRCh38.p7 | 14:88729580 | GTTTTTTGTTTTTTT[G/T]AGACAGAGTCTCACT | 161436 |
rs80233748 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | EML5 | GRCh38.p7 | 14:88651878 | CATTAATGAAGACCT[A/G]CTATCTAAATTCTTG | 161436 |
rs80246247 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EML5 | GRCh38.p7 | 14:88765102 | AACAAGGGTATTATA[C/T]TAGTTTTCTATGCTG | 161436 |
rs80250409 | snp | A/G | 0.0399052 | 0.1355 | intron-variant | EML5 | GRCh38.p7 | 14:88668371 | CAGAAAAAGGGAGTC[A/G]GTGAAGTAGAGAGAA | 161436 |
rs80273667 | snp | A/C | 0.0178098 | 0.0926698 | intron-variant, downstream-variant-500B | EML5 | GRCh38.p7 | 14:88626634 | AAAAAAAAAAAAATC[A/C]TTTTCCCCCTCTCAT | 161436 |
rs80298352 | snp | A/G | | | intron-variant | EML5 | GRCh38.p7 | 14:88624042 | CCTGTATTGAAATGT[A/G]CTTCTTAGTCAACTA | 161436 |
rs111245100 | snp | A/C | 0.5 | 0 | intron-variant | EML5 | GRCh38.p7 | 14:88759698 | CTTAAAAAAAAAAAA[A/C]AAAAAACTGGGGAGA | 161436 |
rs111267140 | snp | A/C | 0.5 | 0 | intron-variant | EML5 | GRCh38.p7 | 14:88685573 | TCAAGTCCCTCATAT[A/C]AAATGGTGTAGTATT | 161436 |
rs111271959 | snp | C/G | 0.0490535 | 0.14873 | intron-variant | EML5 | GRCh38.p7 | 14:88671516 | CAACATAACCAGCTA[C/G]CATCACGATGACAGG | 161436 |
rs111328092 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EML5 | GRCh38.p7 | 14:88744649 | TAAATACATGCAAAA[C/T]ATTTTGTTACAAAAG | 161436 |
rs111334033 | snp | G/T | 0.5 | 0 | intron-variant | EML5 | GRCh38.p7 | 14:88711300 | GAGGTGATCGAATCA[G/T]GGGGGCAGTTTCCCC | 161436 |
rs111336868 | snp | A/C | 0.5 | 0 | intron-variant | EML5 | GRCh38.p7 | 14:88783803 | AATGTGCACTATAGA[A/C]CAAATGGATCTAATA | 161436 |
rs111347045 | snp | A/G | 0.5 | 0 | intron-variant | EML5 | GRCh38.p7 | 14:88656469 | CTGGGGCCTGTCAGG[A/G]AGTGGGGAGCTAGGG | 161436 |
rs111370714 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | EML5 | GRCh38.p7 | 14:88732277 | CCAGTTTCAGCTTTC[C/T]ACATATGGCTAGCCA | 161436 |
rs111381969 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | EML5 | GRCh38.p7 | 14:88754928 | TTGTGTCTCAGCCTC[C/T]TGAGTAGCTGGGATT | 161436 |
rs111452599 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | EML5 | GRCh38.p7 | 14:88763663 | CCATTTTATGAGGCC[A/G]GCATCATCCTGATAC | 161436 |
rs111478925 | snp | C/T | 0.184521 | 0.241273 | intron-variant | EML5 | GRCh38.p7 | 14:88674728 | GCATTAACTCAAAAG[C/T]CCACAGTCTAACATC | 161436 |
rs111535729 | snp | C/T | 0.5 | 0 | intron-variant | EML5 | GRCh38.p7 | 14:88714223 | AATTAGTTCCACCCA[C/T]AAAAATGGCATTTTT | 161436 |
rs111576088 | snp | C/G | 0.0498117 | 0.149749 | intron-variant | EML5 | GRCh38.p7 | 14:88641147 | TCAAAAAGCCCTGGA[C/G]CAGATGGATTCAGAG | 161436 |
rs111596033 | snp | G/T | 0.5 | 0 | intron-variant | EML5 | GRCh38.p7 | 14:88656482 | GGGAGTGGGGAGCTA[G/T]GGGAGGGATAGCATT | 161436 |
rs111605174 | in-del | -/T | 0.5 | 0 | intron-variant | EML5 | GRCh38.p7 | 14:88729559 | CATATACTTATTTGG[-/T]TTTTTTGTTTTTTGT | 161436 |
rs111654627 | snp | A/G | 0.0607341 | 0.163335 | intron-variant | EML5 | GRCh38.p7 | 14:88644959 | TCAGGTGATCGGCCC[A/G]CCTGGGCCTCCCAGA | 161436 |
rs111662812 | snp | A/G | 0.5 | 0 | utr-variant-5-prime, upstream-variant-2KB | EML5 | GRCh38.p7 | 14:88792571 | CGGCGGCGGCCCGGC[A/G]ACGAAAGCCCTCCCG | 161436 |
rs111774430 | snp | C/T | 0.046775 | 0.145601 | intron-variant | EML5 | GRCh38.p7 | 14:88773206 | TCATAGTACACCTCA[C/T]TTGATATCATACAGG | 161436 |
rs111790758 | snp | A/T | 0.5 | 0 | intron-variant | EML5 | GRCh38.p7 | 14:88643976 | CCTTCTTCCTCAATT[A/T]TTACGTAAGGTTACT | 161436 |
rs111876990 | snp | C/T | 0.5 | 0 | intron-variant | EML5 | GRCh38.p7 | 14:88661094 | GGGATAAAAGGAATG[C/T]GTCTCTCTCTCTGAC | 161436 |
rs111889463 | snp | A/T | 0.5 | 0 | intron-variant | EML5 | GRCh38.p7 | 14:88637905 | TTTACTTTTAAAAGT[A/T]GAAAACTGTACAAAA | 161436 |
rs111907868 | snp | A/G | 0.5 | 0 | intron-variant | EML5 | GRCh38.p7 | 14:88728525 | AAAACAATTAAGAAA[A/G]TCATAAGGAAGAGAA | 161436 |
rs111923098 | snp | A/T | 0.5 | 0 | intron-variant | EML5 | GRCh38.p7 | 14:88699474 | TTTATCTCTTATCAT[A/T]TATAGCTTGTGGCTA | 161436 |
rs111928859 | snp | A/T | 0.5 | 0 | intron-variant | EML5 | GRCh38.p7 | 14:88650062 | AAAATGTCTAACTTA[A/T]GTCACATTGGTTTAA | 161436 |
rs111938176 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | EML5 | GRCh38.p7 | 14:88724255 | ACTCCAGCCTTGTGA[C/T]AGAGCAAGACTCCAT | 161436 |
rs112014467 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | EML5 | GRCh38.p7 | 14:88788202 | AAAAATCTATCTACC[A/G]TGCAAATGTTATTCT | 161436 |
rs112068593 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EML5 | GRCh38.p7 | 14:88722331 | TATGTTCACTGCAGC[A/G]CTATTCACAATAACA | 161436 |
rs112141843 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | EML5 | GRCh38.p7 | 14:88631011 | CTGCTGTAAAATGCA[C/G]ACACCCACTGAAGTT | 161436 |
rs112143883 | snp | C/T | | | intron-variant | EML5 | GRCh38.p7 | 14:88684449 | TGCTGGGATTACAGG[C/T]GTGAGCCACCGCGCC | 161436 |
rs112165447 | snp | C/T | 0.5 | 0 | intron-variant | EML5 | GRCh38.p7 | 14:88745691 | ATGGGTGTCTGCATA[C/T]GTCAAACCCATCAAA | 161436 |
rs112182941 | in-del | -/T | 0.5 | 0 | downstream-variant-500B, utr-variant-3-prime | EML5, ZC3H14 | GRCh38.p7 | 14:88614412 | AATCACTGGTTATGC[-/T]TTCTGTGATGTAATT | 161436 |
rs112191983 | snp | C/T | 0.5 | 0 | intron-variant | EML5 | GRCh38.p7 | 14:88671843 | GATCAATTCAACAAG[C/T]AAAGCTAACTATCCT | 161436 |
rs112201826 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | EML5 | GRCh38.p7 | 14:88742825 | ACCAGAATAACAAAT[C/T]AAGAATTGCAGCAGC | 161436 |
rs112271119 | snp | G/T | 0.0456336 | 0.143994 | intron-variant | EML5 | GRCh38.p7 | 14:88721249 | CTGATATTCTTCAAA[G/T]AATTAGAAAAAAACT | 161436 |
rs112275486 | snp | G/T | 0.5 | 0 | intron-variant | EML5 | GRCh38.p7 | 14:88728776 | ATCATTTTATATAAT[G/T]AACTTGAACATCCAC | 161436 |
rs112343449 | in-del | -/AAAAAAG | 0.499598 | 0.0141716 | intron-variant | EML5 | GRCh38.p7 | 14:88660748 | TCCATCTCAGGGAAA[-/AAAAAAG]AAAAAAGAAAAAAGA | 161436 |
rs112402034 | snp | G/T | 0.5 | 0 | intron-variant | EML5 | GRCh38.p7 | 14:88650617 | TATTTGATAAGTATT[G/T]AATTGTTTTTAATTT | 161436 |
rs112422451 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | EML5 | GRCh38.p7 | 14:88721962 | GGCAAAGGACATGAG[C/T]GGACACTTTTTGAAA | 161436 |
rs112455950 | snp | C/T | 0.5 | 0 | intron-variant | EML5 | GRCh38.p7 | 14:88674420 | AAGCAGGCACCTTCT[C/T]CACAGGGCAGCAGGA | 161436 |
rs112488102 | snp | A/G | 0.0948562 | 0.196037 | intron-variant | EML5 | GRCh38.p7 | 14:88647421 | AAGGCATAAGGCTGG[A/G]CACAGTGGCTCACAC | 161436 |
rs112669168 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | EML5 | GRCh38.p7 | 14:88752797 | CCAAACTCCACTGGC[A/G]GAGGAGCAAAACAGC | 161436 |
rs112680595 | snp | C/T | 0.5 | 0 | intron-variant | EML5 | GRCh38.p7 | 14:88717515 | TGTAATCCCAGCAGT[C/T]TGGGAGGCTGAGGCG | 161436 |
rs112725596 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | EML5 | GRCh38.p7 | 14:88650432 | GCACTCCAGCCTGGG[C/T]GACACAGCAAGACTC | 161436 |
rs112745643 | snp | C/G | 0.5 | 0 | intron-variant | EML5 | GRCh38.p7 | 14:88790530 | CCAAATAAATCATAT[C/G]TAGTTTCAGAAGACC | 161436 |
rs112769195 | in-del | -/C | 0.190833 | 0.242898 | intron-variant | EML5 | GRCh38.p7 | 14:88785739 | CTTTCACTGTTACCA[-/C]CCCAGTCCAAGCCAC | 161436 |
rs112771025 | snp | C/G | | | upstream-variant-2KB | EML5 | GRCh38.p7 | 14:88792990 | GGGCGCGCGGCCTTG[C/G]GTGGCCCCGCCCCCT | 161436 |
rs112772108 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | EML5 | GRCh38.p7 | 14:88672963 | TACCAGAGGTACAAA[A/G]AGGAGCTGGTACCAT | 161436 |
rs112928786 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | EML5 | GRCh38.p7 | 14:88675531 | CCGTGGCCTGGCCCA[A/C]AAAACCATCTTTTCC | 161436 |
rs112945623 | snp | C/T | | | intron-variant | EML5 | GRCh38.p7 | 14:88622763 | TTCATTATTGGCTAC[C/T]ATAATTTTTATTATA | 161436 |
rs112968893 | snp | A/G | 0 | 0 | intron-variant | EML5 | GRCh38.p7 | 14:88654019 | TAGTCTTGGGAGGGT[A/G]TATGTGTCCAGGAAT | 161436 |
rs113030331 | snp | C/T | 0.5 | 0 | intron-variant | EML5 | GRCh38.p7 | 14:88638958 | TTTAAGATGTAACAG[C/T]CAAAAGCACTTACCC | 161436 |
rs113031921 | snp | A/G | 0.190205 | 0.242744 | intron-variant | EML5 | GRCh38.p7 | 14:88687996 | GGATTTCTTGAGCCC[A/G]GGAGCTGGAGGCTGC | 161436 |
rs113066740 | snp | C/T | 0.0490535 | 0.14873 | intron-variant | EML5 | GRCh38.p7 | 14:88672286 | ATTGAACAACCTGCT[C/T]CTAAATGACTCCTGG | 161436 |
rs113075751 | snp | C/T | 0.5 | 0 | intron-variant | EML5 | GRCh38.p7 | 14:88704494 | ACTATTATCTCCATT[C/T]TACAGACAGAAAAAA | 161436 |
rs113120293 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EML5 | GRCh38.p7 | 14:88687021 | ACTAATATTTTACCA[C/T]GTGTATCATAGAAAA | 161436 |
rs113155676 | snp | A/G | 0.5 | 0 | intron-variant | EML5 | GRCh38.p7 | 14:88672660 | TTAGCTAGACAAGAA[A/G]AGAGAGAAGAATCAA | 161436 |
rs113185821 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | EML5 | GRCh38.p7 | 14:88764225 | TTTTCTTCAAATGTT[C/T]GTCTGGATTTTGTAT | 161436 |
rs113201733 | snp | A/G | 0.0486741 | 0.148216 | intron-variant | EML5 | GRCh38.p7 | 14:88660202 | GTGGGAGGATAACTT[A/G]GGTCTGGAAGGTCGA | 161436 |
rs113220392 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | EML5 | GRCh38.p7 | 14:88701075 | TATGAGGGTTTCTTC[A/G]ATTCTACTGGGCAAA | 161436 |
rs113252407 | snp | A/G | 0.5 | 0 | intron-variant | EML5 | GRCh38.p7 | 14:88729109 | TATATATAACCAACT[A/G]AGAATGGCAGTTATT | 161436 |
rs113262575 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | EML5 | GRCh38.p7 | 14:88674802 | AATCAAAAGCAAGTT[A/T]CTTACTTCCTAGATA | 161436 |
rs113264537 | snp | C/G/T | 0.5 | 0 | intron-variant | EML5 | GRCh38.p7 | 14:88762386 | GTGGTGGCACATGCC[C/G/T]GTAATCCCAGCTACT | 161436 |
rs113266558 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | EML5 | GRCh38.p7 | 14:88754963 | GCACCCGCCACCACG[C/T]CCAGCTAATTTTTGT | 161436 |
rs113311532 | snp | C/G | | | intron-variant | EML5 | GRCh38.p7 | 14:88684445 | AAAGTGCTGGGATTA[C/G]AGGCGTGAGCCACCG | 161436 |
rs113343100 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | EML5 | GRCh38.p7 | 14:88773597 | CTGCATATTACAATC[A/C]TTTGGGAAGCTTAAA | 161436 |
rs113514761 | snp | G/T | 0.5 | 0 | intron-variant | EML5 | GRCh38.p7 | 14:88691213 | TCTATGTGTCACTGG[G/T]GTAGTGAAGCTCACT | 161436 |
rs113517686 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | EML5 | GRCh38.p7 | 14:88720677 | CAATATCATACTGAA[C/T]GTGCAAAAGCTGGAA | 161436 |
rs113664369 | snp | C/T | | | intron-variant | EML5 | GRCh38.p7 | 14:88693946 | CAGCTAATTTTTTTT[C/T]TTTTTTTGTAGAGAC | 161436 |
rs113709296 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | EML5 | GRCh38.p7 | 14:88727026 | GGAATGTGCCACCCA[A/G]CCTGGCTATGTTTTG | 161436 |
rs113729678 | snp | C/T | 0 | 0 | intron-variant | EML5 | GRCh38.p7 | 14:88775460 | TGGGCCTTAAGGGAA[C/T]ATTGGCAGTAGTCTG | 161436 |
rs113758331 | snp | A/G | 0.190205 | 0.242744 | intron-variant | EML5 | GRCh38.p7 | 14:88729742 | ATTTTTGTATTTTTA[A/G]TAGAGACAGGGTTTT | 161436 |
rs113805688 | snp | C/T | 0.5 | 0 | intron-variant | EML5 | GRCh38.p7 | 14:88640057 | GTTGGATCCAGAGGA[C/T]AGAGAAACCATGAAT | 161436 |
rs113826299 | snp | C/T | 0.5 | 0 | intron-variant | EML5 | GRCh38.p7 | 14:88673288 | TAAAGACAAAGACCA[C/T]ATGATTATCTCAGTA | 161436 |
rs113886123 | snp | C/G | 0 | 0 | intron-variant | EML5 | GRCh38.p7 | 14:88781941 | ATACCCAAAAATGTG[C/G]AAGTGACTTTGTAAC | 161436 |
rs113890578 | snp | C/G | | | intron-variant | EML5 | GRCh38.p7 | 14:88684866 | CGTTAAAATTTTTTT[C/G]TGTATACATTAAATT | 161436 |
rs113905377 | snp | A/G | 0.5 | 0 | intron-variant | EML5 | GRCh38.p7 | 14:88734815 | TTAGCCAAATCCAGA[A/G]TGTGGGAAACGCTGA | 161436 |
rs113923121 | snp | C/G/T | 0.5 | 0 | intron-variant | EML5 | GRCh38.p7 | 14:88704495 | CTATTATCTCCATTT[C/G/T]ACAGACAGAAAAAAA | 161436 |
rs113989318 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | EML5 | GRCh38.p7 | 14:88670579 | TGAGATGGATGAATT[A/G]ACAGAAGTAGGCTTC | 161436 |
rs113998536 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | EML5 | GRCh38.p7 | 14:88686755 | GTTCAAGGTTTCAGT[A/G]AGTTATGATTGCACC | 161436 |
rs114018029 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | EML5 | GRCh38.p7 | 14:88676790 | ACAAAAACAGACACA[C/T]AGACCAAGGGAATAG | 161436 |
rs114021104 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | EML5 | GRCh38.p7 | 14:88781188 | ATGCTCATGCTGTTT[C/T]CTGTGCATATACAAA | 161436 |
rs114063242 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | EML5 | GRCh38.p7 | 14:88624866 | ATGAGGAGGAAGGTC[A/G]GAGAGGACACTCTGT | 161436 |
rs114068875 | snp | A/G | 0.0107246 | 0.0724382 | utr-variant-3-prime, nc-transcript-variant | EML5 | GRCh38.p7 | 14:88615399 | ATAAAATATTTCATT[A/G]AACAATGAACCTTGA | 161436 |
rs114085148 | snp | G/T | 0.00914312 | 0.0669923 | intron-variant | EML5 | GRCh38.p7 | 14:88732888 | CGATCTCAGCTTATT[G/T]CAACTTCTGCCTCCC | 161436 |
rs114090036 | snp | C/T | 0.0399052 | 0.1355 | intron-variant | EML5 | GRCh38.p7 | 14:88688864 | CATGCCAACCTCATC[C/T]CCCTTCTTCACGCTT | 161436 |
rs114107817 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | EML5 | GRCh38.p7 | 14:88625807 | TTCTCAAAAATGTAA[A/G]TGTACTTAAATATTC | 161436 |
rs114150199 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | EML5 | GRCh38.p7 | 14:88739758 | TTAATAACCCTAATA[C/T]TCAAATGAATAAAGG | 161436 |
rs114173338 | snp | A/G | 0.0256215 | 0.110247 | intron-variant | EML5 | GRCh38.p7 | 14:88721348 | GGCAGGAAGCATCAC[A/G]CTACTGAACCTCAAA | 161436 |
rs114182796 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | EML5 | GRCh38.p7 | 14:88727190 | ACTCAAAGTCCAATT[C/T]TATCTTTTTCCTCTT | 161436 |
rs114210828 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | EML5 | GRCh38.p7 | 14:88627372 | CAATCAAATCATTAA[C/T]AATAAATACATAGTT | 161436 |
rs114226362 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | EML5 | GRCh38.p7 | 14:88721990 | AAAGACAACATTTAT[A/G]TGGCCAACAAACATA | 161436 |
rs114228319 | snp | C/T | 0.168785 | 0.236441 | intron-variant | EML5 | GRCh38.p7 | 14:88784887 | TCAAGGAGATATCTA[C/T]ACTCCAATGTTTGTT | 161436 |
rs114289261 | snp | A/G | 0.0399052 | 0.1355 | intron-variant | EML5 | GRCh38.p7 | 14:88753996 | AAAAAAATTAGCCAG[A/G]CATGATGGTATGTGC | 161436 |
rs114296821 | snp | A/G | 0.0092289 | 0.0672999 | intron-variant | EML5 | GRCh38.p7 | 14:88704993 | CCTTTAAAAATGTAT[A/G]CAAGTAGAAATATTC | 161436 |
rs114356904 | snp | C/T | 0.0109408 | 0.0731486 | intron-variant | EML5 | GRCh38.p7 | 14:88694280 | TTTCTTAAAATTCTA[C/T]GGAGTAAAAAAGAAG | 161436 |
rs114363610 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | EML5 | GRCh38.p7 | 14:88776942 | ATAAGATCTAGAAAA[C/T]AGTCTCAAAAGGGCA | 161436 |
rs114434862 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | EML5 | GRCh38.p7 | 14:88684103 | ACTAATAAATGAGGA[C/T]GGCAAGTTTACAGGT | 161436 |
rs114436908 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | EML5 | GRCh38.p7 | 14:88738133 | TAAGCTTTAAAGCAC[A/C]ATAATGTTTAGCAAA | 161436 |
rs114467663 | snp | C/T | 0.0314385 | 0.121371 | intron-variant | EML5 | GRCh38.p7 | 14:88633938 | TACTATTACCACAGA[C/T]TGAGTTCAGAATCAT | 161436 |
rs114498840 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | EML5 | GRCh38.p7 | 14:88719214 | AAATGACAAGACCAC[A/G]TCTCTACAAAAAATT | 161436 |
rs114498909 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | EML5 | GRCh38.p7 | 14:88639877 | TGAGCCACCGTGCCC[A/G]GCAGGAATTGAAGTT | 161436 |
rs114539008 | snp | C/G | 0.00953873 | 0.0683987 | intron-variant | EML5 | GRCh38.p7 | 14:88736695 | CTAAGACAGTTTAAA[C/G]CCTGAAAGCCAAGCT | 161436 |
rs114635838 | snp | C/G | 0.0322114 | 0.122752 | intron-variant | EML5 | GRCh38.p7 | 14:88653988 | ATTGGTCTATTCAGG[C/G]ATTCCACTTCTGGTT | 161436 |
rs114637694 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | EML5 | GRCh38.p7 | 14:88663490 | TGAATACATGAAACA[A/G]TAACATCCTTAAAAA | 161436 |
rs114708598 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | EML5 | GRCh38.p7 | 14:88753229 | CCTCTCACCTGCATG[C/T]CCCACTCCCACAAGG | 161436 |
rs114709055 | snp | C/G | 0.0193772 | 0.0965046 | intron-variant | EML5 | GRCh38.p7 | 14:88784198 | TACATCAAAAAAAAG[C/G]AAAAACTTCAAATAA | 161436 |
rs114767620 | snp | A/T | 0.00914312 | 0.0669923 | intron-variant | EML5 | GRCh38.p7 | 14:88705948 | ATAATTTTTGTCAAT[A/T]AAAGCATTTACAAAA | 161436 |
rs114769440 | snp | G/T | 0.00795532 | 0.062565 | intron-variant | EML5 | GRCh38.p7 | 14:88677415 | TTCAATTATGAAAAT[G/T]TCAAAAGCAATTGCA | 161436 |
rs114777381 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | EML5 | GRCh38.p7 | 14:88725426 | TGTATCTGTTCATAA[C/T]GGGGAGATGTTAGTT | 161436 |
rs114840889 | snp | C/G | 0.00795532 | 0.062565 | utr-variant-3-prime, nc-transcript-variant | ZC3H14 | GRCh38.p7 | 14:88613101 | GTTGTGTTGCCATTG[C/G]TTTTCCATTGGGAGA | 161436 |
rs114852901 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | EML5 | GRCh38.p7 | 14:88675259 | AGAGGTTCTTCATGA[A/G]GTCCCTGCCTCTGCA | 161436 |
rs114880149 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | EML5 | GRCh38.p7 | 14:88755478 | AGGTCACCCATAATT[C/T]GCAAAAAAAAATCTA | 161436 |
rs114886016 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | EML5 | GRCh38.p7 | 14:88750459 | ACCTCACAGGGGTTA[C/T]TGTGAAAATTGACAT | 161436 |
rs114891926 | snp | C/T | 0.0325976 | 0.123435 | intron-variant | EML5 | GRCh38.p7 | 14:88781518 | CTTCTTTTGTATATC[C/T]TTATCCCCTCTTTGC | 161436 |
rs114893438 | snp | C/T | 0.0310518 | 0.120672 | intron-variant | EML5 | GRCh38.p7 | 14:88648816 | GTGCTTTATTTCTGG[C/T]AAAATAGTATAAGAT | 161436 |
rs114984584 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | EML5 | GRCh38.p7 | 14:88721730 | TTTCATGAAGAAATC[A/G]CTAAAAGCAGCTGCA | 161436 |
rs114989285 | snp | C/T | 0.0271762 | 0.113356 | intron-variant, downstream-variant-500B | EML5 | GRCh38.p7 | 14:88622418 | GACAGAATAGCTTCC[C/T]AGCTTATGCACCACA | 161436 |
rs114994232 | snp | A/C | 0.00795532 | 0.062565 | intron-variant | EML5 | GRCh38.p7 | 14:88742713 | AATACCTTCACAGTG[A/C]TTATATCATGTGCCT | 161436 |
rs114994561 | snp | A/G | 0.0333695 | 0.124785 | intron-variant | EML5 | GRCh38.p7 | 14:88741404 | AAGCTTAAAAAAATA[A/G]GATAGATGTCCATGT | 161436 |
rs114996841 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | EML5 | GRCh38.p7 | 14:88767908 | CATTTTTTCCACTAA[C/T]GTCTCTTTTCTGTTC | 161436 |