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 |