SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs2958 | snp | A/G | 0.441705 | 0.160466 | utr-variant-3-prime | NSMCE1 | GRCh38.p7 | 16:27225082 | TGGAACCTGAAACAC[A/G]GACGCCTTTCTTCCA | 197370 |
rs1127228 | snp | A/G | 0.449078 | 0.151221 | synonymous-codon | NSMCE1 | GRCh38.p7 | 16:27226789 | CATCCTGGAGATGGA[A/G]CAATACATCCGGGAG | 197370 |
rs3211442 | snp | C/G | 0 | 0 | missense | NSMCE1 | GRCh38.p7 | 16:27233042 | AAGAAGGAAGCGGAG[C/G]AGGTGCTGCAGAAGT | 197370 |
rs4238951 | snp | A/T | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27251205 | AAATATATATATATA[A/T]ATAAAACTCTGTAGA | 197370 |
rs4238952 | snp | C/T | 0.119978 | 0.213528 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27254149 | ATAGGAAATTAATAA[C/T]ATTGGGTCTTGCGAG | 197370 |
rs4267310 | snp | A/G | 0.11963 | 0.213316 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27252650 | ttagccgggcgcggt[A/G]gctcatgcctgtaat | 197370 |
rs4349150 | snp | A/G | 0.11963 | 0.213316 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27252581 | tgagcctaggtgttc[A/G]agaccagcctaggcc | 197370 |
rs4398114 | snp | A/C | 0 | 0 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27249362 | gactaatcataggtc[A/C]cagaggttttctcct | 197370 |
rs4399540 | snp | A/G | 0.499382 | 0.017561 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27265142 | ttcatctgctgctgg[A/G]agagtataaattctt | 197370 |
rs4410081 | snp | C/T | 0.464841 | 0.127841 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27244028 | TTCTAACCAATCACA[C/T]AGGACGCCCCACTTC | 197370 |
rs4414501 | snp | A/G | 0.163892 | 0.234703 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27251522 | attagatttgccaca[A/G]ttgggtttagcacgt | 197370 |
rs4468629 | snp | G/T | 0.0310518 | 0.120672 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27249633 | cccttcatctgtttg[G/T]ccatcatgacatgac | 197370 |
rs4493040 | snp | A/G | 0.157642 | 0.232314 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27235617 | CCAATCAGCACCTTC[A/G]GCGCATTACTCAATG | 197370 |
rs4499236 | snp | C/T | 0.430136 | 0.173352 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27242810 | GAGTGGCAGCTCTGA[C/T]ACCTTCTGTGGCGCT | 197370 |
rs4523932 | snp | A/G | 0.119978 | 0.213528 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27265406 | ctcctggactcaagc[A/G]atccacccacctcag | 197370 |
rs4531736 | snp | C/T | 0.0236746 | 0.106192 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27242858 | CCATGCAGGAGCCCT[C/T]GCAGAGCTGATACAG | 197370 |
rs4536480 | snp | C/T | 0.464523 | 0.128375 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27243681 | TTAGAGATGGGGTCT[C/T]GCTCTGTCATCTAGG | 197370 |
rs4545819 | snp | C/T | 0.438946 | 0.163706 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27252452 | TGGGATTATTTTTCT[C/T]AGAGTGTGCCAAATT | 197370 |
rs4553636 | snp | C/T | 0.093777 | 0.195178 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27235448 | TTGGGTGAACGCCAA[C/T]GCCACGTGGCTTCTT | 197370 |
rs4553637 | snp | C/T | 0.387074 | 0.209071 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27243639 | GATCAGTAACTGATA[C/T]TACCCTAATTGATTT | 197370 |
rs4591148 | snp | C/G | 0 | 0 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27249365 | taatcataggtcaca[C/G]aggttttctcctatg | 197370 |
rs4591150 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant, utr-variant-5-prime | NSMCE1, FLJ21408 | GRCh38.p7 | 16:27268260 | GTAAGAAACTCCGTA[C/T]ACAAAACAGAGGGGA | 197370 |
rs4787415 | snp | A/G | 0.391024 | 0.206427 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27239885 | GATTTCTTAAGGGCT[A/G]TAGTAAAGTAGCTCA | 197370 |
rs4787417 | snp | A/G | 0.11963 | 0.213316 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27255496 | TCTAGGGATTCCCAG[A/G]GTAGGTTATCAGTAG | 197370 |
rs4787418 | snp | A/G | 0.499424 | 0.0169631 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27259751 | CCTAGGCTCATCCTA[A/G]TAAAACCACACAATA | 197370 |
rs4787419 | snp | C/G | 0.499424 | 0.0169631 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27259896 | CTTCTATGCTGGGAG[C/G]GGGTGTCTCAACAGA | 197370 |
rs4787420 | snp | A/C | 0.121022 | 0.21416 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27263190 | cccagcaaccccatt[A/C]ctgggtatataccag | 197370 |
rs4787421 | snp | A/G | 0.0360663 | 0.129354 | upstream-variant-2KB, intron-variant | NSMCE1, FLJ21408 | GRCh38.p7 | 16:27270310 | ttttgtaagcaccca[A/G]tggttctccttgcct | 197370 |
rs4787422 | snp | A/G | 0.488545 | 0.074807 | upstream-variant-2KB, intron-variant | NSMCE1, FLJ21408 | GRCh38.p7 | 16:27270570 | gtcagatcctgggtt[A/G]ggaccataggaccag | 197370 |
rs4787941 | snp | C/T | 0.39121 | 0.2063 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27238955 | GCTCACAGCAACCTC[C/T]ACCTCCCAGGTTCAA | 197370 |
rs4787943 | snp | C/T | 0.164546 | 0.234942 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27248114 | ACTGCAAATGGACAA[C/T]TAGGTGTTCACATTT | 197370 |
rs4787944 | snp | A/G | 0.11963 | 0.213316 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27251568 | tgaggagtcttgttt[A/G]gggttttctttcctc | 197370 |
rs4787945 | snp | A/G | 0.490997 | 0.0664859 | upstream-variant-2KB, intron-variant | NSMCE1, FLJ21408 | GRCh38.p7 | 16:27270481 | taatttggtggctgg[A/G]ggggctggggattag | 197370 |
rs4787946 | snp | G/T | 0.492918 | 0.0590819 | upstream-variant-2KB, intron-variant | NSMCE1, FLJ21408 | GRCh38.p7 | 16:27270484 | TTTGGTGGCTGGAGG[G/T]GCTGGGGATTAGAGA | 197370 |
rs5816427 | in-del | -/T | 0 | 0 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27265170 | TTTTTTTTTTTTTTT[-/T]GAGACAGGGTCTCAC | 197370 |
rs5816428 | in-del | -/A | 0.498206 | 0.0298983 | intron-variant, upstream-variant-2KB | NSMCE1, FLJ21408 | GRCh38.p7 | 16:27266622 | AAAAGAAAAAAAAAA[-/A]TTACTTTTTTTAAAA | 197370 |
rs6498003 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27247265 | tgacagtgagtgagt[A/T]ctcaagagatctgac | 197370 |
rs6498004 | snp | C/G | 0.439085 | 0.163545 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27248875 | cctctgtcacccaag[C/G]tgaagtgcagtggca | 197370 |
rs6498005 | snp | C/T | 0.120326 | 0.21374 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27258879 | gctcagcctcccaag[C/T]agctggaactacagg | 197370 |
rs6498007 | snp | A/G | 0.48692 | 0.0798058 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27265330 | cacaccactatgccc[A/G]gctaatttctgtatt | 197370 |
rs7184503 | snp | C/G | 0.164546 | 0.234942 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27259016 | cagcctcccaaagtg[C/G]tgggattacagtgtg | 197370 |
rs7186151 | snp | A/G | 0.442385 | 0.15965 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27238060 | CAGCTCCTCTTAATC[A/G]TGACCTGAGAAGAAA | 197370 |
rs7186985 | snp | C/T | 0.45645 | 0.140991 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27237922 | ACACCAGCCACTGCT[C/T]GGGCGCTCCCGTTCT | 197370 |
rs7187853 | snp | A/G | 0.11963 | 0.213316 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27256082 | TTTTGCCTTTTTTTT[A/G]TGTCCCTTCACCTGT | 197370 |
rs7188707 | snp | A/T | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27262974 | tgatcattagagaaa[A/T]gcaaatcaaaaccac | 197370 |
rs7189192 | snp | C/T | 0.492533 | 0.0606443 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27255988 | GACAGGAGGGACACC[C/T]TTTCTGGTGTCCCTT | 197370 |
rs7189678 | snp | A/C/G | 0.164219 | 0.234823 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27250959 | caattctcctgcctc[A/C/G]gcctcccgagcagct | 197370 |
rs7191348 | snp | C/T | 0.0256215 | 0.110247 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27230154 | TCTCAGAGGCCTCCC[C/T]GCTGACCCCAACCAC | 197370 |
rs7192633 | snp | C/T | 0.478768 | 0.100824 | downstream-variant-500B | NSMCE1 | GRCh38.p7 | 16:27224774 | TCACACATCCAGGTT[C/T]GGGCCAGCCCAGTCC | 197370 |
rs7194857 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27265533 | atttgcatatccccc[A/G]aaatctactattagg | 197370 |
rs7195194 | snp | A/C/G | 0.0653224 | 0.168525 | missense, utr-variant-5-prime | NSMCE1 | GRCh38.p7 | 16:27257458 | ACCTTGTAGCAGTGC[A/C/G]TCTGCAAGCGCTTCA | 197370 |
rs7195219 | snp | A/G | 0.438946 | 0.163706 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27265735 | tcctcacatcaacac[A/G]catacttctcagaaa | 197370 |
rs7195953 | snp | A/G | 0.472147 | 0.114677 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27266104 | TGGgctgggcatggt[A/G]attcacacctgtaat | 197370 |
rs7200553 | snp | A/G | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27257703 | AAAGTCATTCTTCAT[A/G]CTGTTTACTACAAAG | 197370 |
rs7200596 | snp | G/T | 0.119978 | 0.213528 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27257760 | ATCAGGACTGGGCag[G/T]ggtaagaggtgtgga | 197370 |
rs7201652 | snp | C/T | 0.438946 | 0.163706 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27257702 | AAAAGTCATTCTTCA[C/T]GCTGTTTACTACAAA | 197370 |
rs7201783 | snp | C/G | 0.455621 | 0.142197 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27228193 | CACAGTGCGTTCGCT[C/G]TGGAACACCAGTAGA | 197370 |
rs7350846 | snp | C/T | 0 | 0 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27235490 | TACTTGGAAGACAAA[C/T]AGACAACAGATGGAG | 197370 |
rs7359366 | snp | C/T | 0 | 0 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27242213 | CATATAACTTGACTC[C/T]TTGACCCTCATGAAT | 197370 |
rs7359403 | snp | C/T | 0.119281 | 0.213102 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27248234 | ggaatggctgaatca[C/T]aggaaattgccacac | 197370 |
rs7359408 | snp | C/T | 0 | 0 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27242520 | TTATGGTACTAAAAC[C/T]TATGACACCACTGCA | 197370 |
rs7498181 | snp | C/G | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27228924 | GGCAACCCACCTCCC[C/G]GGCCTCCACCCTCTT | 197370 |
rs8052566 | snp | C/T | 0.483995 | 0.0880135 | upstream-variant-2KB, intron-variant | NSMCE1, FLJ21408 | GRCh38.p7 | 16:27269311 | TGTAATCCCAGCTAC[C/T]CGGGAGGCTGAGGCA | 197370 |
rs9673181 | snp | A/C | 0 | 0 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27241921 | AGCGACAAAGTCTAG[A/C]CCAGAAATCAGATGT | 197370 |
rs9928838 | snp | C/T | 0.031825 | 0.122064 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27253172 | ttctatgaatcattc[C/T]agaaaattatcaaat | 197370 |
rs9930726 | snp | A/G | 0.101658 | 0.201233 | intron-variant, upstream-variant-2KB | NSMCE1, FLJ21408 | GRCh38.p7 | 16:27268026 | ggaattatagccgtg[A/G]gccaccgcgaccagG | 197370 |
rs9939187 | snp | C/T | 0.0456336 | 0.143994 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27231675 | TGAAGAGGGGCTGCA[C/T]CACAAGCGAGAATGG | 197370 |
rs9940555 | snp | C/T | 0.109814 | 0.206997 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27259286 | TCCACACAATCATAC[C/T]ACACACCTGAGCATC | 197370 |
rs10400966 | snp | A/G | 0 | 0 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27245603 | AGACACAAAAGCAAC[A/G]TCAATTTCCTTGTGG | 197370 |
rs10568167 | in-del | -/GATT | 0.030278 | 0.119257 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27236940 | ACCCGTACAACTCAA[-/GATT]CATAAAGTTAAAAAA | 197370 |
rs10578763 | in-del | -/C/CTT | 0 | 0 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27238545 | TCGCCTTTTTTCTTT[-/C/CTT]TTTTTTTTTTACAAT | 197370 |
rs10693168 | in-del | -/CAGC | 0 | 0 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27239962 | TTATTATGTGCCAGC[-/CAGC]ACTATGCATTCACAT | 197370 |
rs11074849 | snp | C/T | 0.499424 | 0.0169631 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27263589 | agaaaatataactat[C/T]gggtactggacttaa | 197370 |
rs11268049 | in-del | -/ATATATATATATATATATATATATATAA | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27251164 | AATTATTTAAAATAT[-/ATATATATATATATATATATATATATAA]ATATATATATATATA | 197370 |
rs11317900 | in-del | -/A | 0 | 0 | intron-variant, upstream-variant-2KB | NSMCE1, FLJ21408 | GRCh38.p7 | 16:27267626 | GATCGGATGCAGGGG[-/A]AAAAAAAAAAAAAGT | 197370 |
rs11420728 | in-del | -/A | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27261183 | AAAAAAAAAAAAAAA[-/A]GAAACTATAAAAAGA | 197370 |
rs11553886 | snp | C/T | 0.000182187 | 0.00954255 | missense | NSMCE1 | GRCh38.p7 | 16:27234228 | TTTCCAAAATGGCTA[C/T]GGATTTTGCAGAGAA | 197370 |
rs11553887 | snp | C/T | | | synonymous-codon, utr-variant-5-prime | NSMCE1 | GRCh38.p7 | 16:27235229 | GGAGTCCTTGTATAT[C/T]GAGATAAAGAGAGGA | 197370 |
rs11553888 | snp | C/T | | | synonymous-codon, utr-variant-5-prime | NSMCE1 | GRCh38.p7 | 16:27235238 | CAGTGTCTTGGAGTC[C/T]TTGTATATTGAGATA | 197370 |
rs11640842 | snp | G/T | 0 | 0 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27238589 | CATTTGCGGTTTTGG[G/T]GAGAGAATAATTCCA | 197370 |
rs11641348 | snp | G/T | 0.427271 | 0.176281 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27233765 | ATGTGCACGTGCAAA[G/T]GATTCAGTGGGCACC | 197370 |
rs11643082 | snp | C/G | 0.496245 | 0.0431677 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27261432 | aatatctgcaattaa[C/G]atacttaaaaatatt | 197370 |
rs11643134 | snp | C/T | 0.439085 | 0.163545 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27231559 | GGAGAATCGCTTGAA[C/T]CCGGGAGGTTGAGGT | 197370 |
rs11644287 | snp | A/G | 0.0298908 | 0.118541 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27245241 | CTGAGACTCAGAAAA[A/G]TAAAAGAACTTTCCC | 197370 |
rs11646066 | snp | A/G | 0.205417 | 0.245993 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27263927 | atgctattacagtca[A/G]catcccaagaggctt | 197370 |
rs11646067 | snp | A/G | 0.451234 | 0.14834 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27233831 | GTGGGGACTGGGACC[A/G]GGCCTTTCTAACAAG | 197370 |
rs11647383 | snp | A/T | 0.452965 | 0.145963 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27234494 | GAACTCCAAAGGGTG[A/T]GCAGTATTTTCCAAA | 197370 |
rs11860191 | snp | C/T | 0.476487 | 0.105846 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27246262 | TGAAGTATTTCTAAA[C/T]CTAAATTTTTAAATC | 197370 |
rs11861096 | snp | C/T | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27248349 | gccttgcagagtctt[C/T]ttcattttagccatt | 197370 |
rs11863220 | snp | A/G | 0 | 0 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27262822 | acctacagaatggga[A/G]aaaatatttgcaaac | 197370 |
rs12102807 | snp | C/T | 0.101658 | 0.201233 | intron-variant, nc-transcript-variant, utr-variant-5-prime | NSMCE1, FLJ21408 | GRCh38.p7 | 16:27268205 | TTTAAACGCATCTGG[C/T]CTCGGGGCTGTAACA | 197370 |
rs12149695 | snp | A/T | 0.386123 | 0.209692 | upstream-variant-2KB, intron-variant | NSMCE1, FLJ21408 | GRCh38.p7 | 16:27270108 | AGCAACTGTGGGTGG[A/T]TAATATTTGTGGGGG | 197370 |
rs12445023 | snp | A/G | 0.46885 | 0.12085 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27255730 | CTTGAAAGAATATTC[A/G]TTTCTGTTCTGTCTC | 197370 |
rs12445506 | snp | A/C | 0.386123 | 0.209692 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27237215 | TGGATGTGGTGAGAT[A/C]GTAACATATGACAAT | 197370 |
rs12446162 | snp | C/T | 0.435263 | 0.167862 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27244808 | TAAGCAGAATGCCAG[C/T]TCCCTGAAGGCTGGG | 197370 |
rs12448009 | snp | A/G | 0.483852 | 0.0883933 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27264816 | ctattcaccaaaaat[A/G]ccagaaaggtggggg | 197370 |
rs12448921 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27236042 | TTTGACTTCTCTGTC[A/G]CCCACCTCCCCTGGC | 197370 |
rs12597361 | snp | G/T | 0 | 0 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27265260 | gcagccttgaccttg[G/T]gggctcaatcgatcc | 197370 |
rs12598841 | snp | C/T | 0.103794 | 0.20279 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27247692 | agcactttgggaggc[C/T]gaggtgggcagatca | 197370 |
rs12598864 | snp | C/T | 0.133435 | 0.221162 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27247770 | tctctaccagaaata[C/T]aaaaaaattagccgg | 197370 |
rs12599550 | snp | A/G | 0 | 0 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27265286 | gatcctctgacctca[A/G]aaccccctagcagct | 197370 |
rs12919473 | snp | A/C | 0.030278 | 0.119257 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27250653 | caaaaattcgtcggg[A/C]gtggtggcacgtgcc | 197370 |
rs12919958 | snp | A/G | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27250946 | tcccggattcaagca[A/G]ttctcctgcctcagc | 197370 |
rs12923010 | snp | G/T | 0.185472 | 0.241529 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27247383 | ccaccatgactgtaa[G/T]tttcctgaggcctcc | 197370 |
rs12924419 | snp | C/T | 0.40086 | 0.199352 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27243007 | GAAAATGGACAAATC[C/T]GATGCCTACAGAGGC | 197370 |
rs12928394 | snp | A/G | 0.432357 | 0.171014 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27227416 | GCAGTGGAGCCTCCA[A/G]TGGAAGCCAGGCCTC | 197370 |
rs12928578 | snp | C/T | 0.102014 | 0.201495 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27257793 | ctggagctagaatgc[C/T]gggattcagggcctg | 197370 |
rs12934078 | snp | A/T | 0.390838 | 0.206555 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27236340 | GTCTTGCTCTCGCCC[A/T]GGCTGGAGTGCAGTA | 197370 |
rs12934276 | snp | A/G | 0.458775 | 0.137524 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27236158 | TCAGCTGAGGAGGAC[A/G]GAGAGGCTGCGGTGA | 197370 |
rs12934556 | snp | C/T | | | intron-variant, upstream-variant-2KB | NSMCE1, FLJ21408 | GRCh38.p7 | 16:27267866 | tccgtctcagcctcc[C/T]gagtagctgggatta | 197370 |
rs12934622 | snp | C/T | 0.465263 | 0.127129 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27244998 | ATTCCTATCACACTA[C/T]CATACCAGCACCATG | 197370 |
rs12934784 | snp | C/G | | | intron-variant, upstream-variant-2KB | NSMCE1, FLJ21408 | GRCh38.p7 | 16:27267782 | tgcccaagctggagt[C/G]aagtggcacgatctt | 197370 |
rs12935512 | snp | C/T | | | intron-variant, upstream-variant-2KB | NSMCE1, FLJ21408 | GRCh38.p7 | 16:27267731 | aacagtgtaaatatA[C/T]GCAtttttttttttg | 197370 |
rs17856580 | snp | C/T | 0.352027 | 0.228233 | missense, utr-variant-5-prime | NSMCE1 | GRCh38.p7 | 16:27235296 | TTATCTACGGTGGCA[C/T]TGCCTGGAAATAAAC | 197370 |
rs28363677 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant, utr-variant-5-prime | NSMCE1 | GRCh38.p7 | 16:27241738 | AGATCACTTAGTGAC[A/G]AACCGTCCTCTCCAT | 197370 |
rs28368200 | snp | A/T | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27251191 | atatatatatatata[A/T]ataaaaCTCTGTAGA | 197370 |
rs28369102 | snp | A/G | 0.00951761 | 0.0683244 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27234308 | GGCTGTGCTCTTTGC[A/G]TGTTGGTTAACGTGT | 197370 |
rs28456036 | snp | A/G | 0.441977 | 0.16014 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27233227 | TACCAAGTCTGGCAG[A/G]GGCACAGTAAAACCA | 197370 |
rs28572393 | snp | C/T | 0.031825 | 0.122064 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27256124 | CTGTGTACCTGTACA[C/T]GCCCTTTCTCATACC | 197370 |
rs28573272 | snp | A/G | 0.0295035 | 0.117819 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27234070 | TTTTCTCAGACAGCA[A/G]TGGTGGCCCATGTCC | 197370 |
rs28580249 | snp | A/T | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27251189 | ATATATATATATATA[A/T]AAATATATATATATA | 197370 |
rs34251671 | in-del | -/G | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27231744 | CCAAATACAGCCTGG[-/G]AGGGCAAGAACAACT | 197370 |
rs34281126 | in-del | -/G | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27232241 | GCACAAGCACCTGGG[-/G]AGGCACAGCTGTGGT | 197370 |
rs34356479 | snp | C/T | 0.383632 | 0.211288 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27230287 | GGTGATATACCCACC[C/T]GGAAGGGCCTTGTCA | 197370 |
rs34561002 | snp | A/G | 0.433673 | 0.1696 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27226081 | GAACGCAGTGACAGA[A/G]GCCGAGGGCTCCCAA | 197370 |
rs34598562 | in-del | -/A | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27260304 | TGGTCAGGAGTAGAA[-/A]GCTGGACATGAATAA | 197370 |
rs34652145 | in-del | -/T | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27226145 | GACAGCCACAGCTTT[-/T]CAGAAGCTTATTTGC | 197370 |
rs34711786 | in-del | -/T | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27246215 | AGCGACCTGGTTTTT[-/T]GCCCAAACATCAAAT | 197370 |
rs34722339 | snp | C/T | 0.441021 | 0.161279 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27239185 | CCGACACATTCCTTT[C/T]TAAGTTGACCAGAAC | 197370 |
rs34735060 | in-del | -/C | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27240696 | CAGGACACTTCTCCC[-/C]TAAGGAGAAGGGTTG | 197370 |
rs34903091 | in-del | -/G | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27232227 | CTCAACACACATGGG[-/G]CACAAGCACCTGGGA | 197370 |
rs34906383 | snp | A/G | 3.32154e-05 | 0.00407512 | missense, utr-variant-5-prime | NSMCE1 | GRCh38.p7 | 16:27257477 | GTGCTAGAGGAATGG[A/G]ACGTGAAGCGCTTGC | 197370 |
rs34913006 | snp | A/G | 0.43221 | 0.171171 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27228065 | GCTGGGATTGCAGGC[A/G]TGAGTCACCGCACCC | 197370 |
rs34932243 | in-del | -/G | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27231078 | GTGTTGTGTACTGGG[-/G]ATGTTGGGGCACTCG | 197370 |
rs34937141 | in-del | -/G | | | intron-variant, utr-variant-5-prime | NSMCE1, FLJ21408 | GRCh38.p7 | 16:27268271 | CGTACACAAAACAGA[-/G]GGGAGCACGGAGGGC | 197370 |
rs34939984 | snp | C/T | 0.432063 | 0.171327 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27234391 | TGTATCCAGGCACTG[C/T]GGGCCGCAGGGATGG | 197370 |
rs34940876 | snp | C/T | 0.449772 | 0.150322 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27226713 | CCGTGCCCTGCCCTG[C/T]GGGTACCTGGATGAG | 197370 |
rs34970492 | in-del | -/TT | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27238555 | TCTTTTTTTTTTTTT[-/TT]ACAATTGTCTTTCTC | 197370 |
rs35025981 | in-del | -/G | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27244482 | GGAAGATGTCTGGGG[-/G]CTCCATCCCCTGACC | 197370 |
rs35069943 | in-del | -/G | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27232597 | CCCAGCCCCGAAGGG[-/G]AAACAACGACTCCCC | 197370 |
rs35071890 | in-del | -/C | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27226994 | TCAGCCACATCCCCC[-/C]TGGCAGAGCCTCGGC | 197370 |
rs35108912 | in-del | -/TT | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27236315 | TTTTTTTTTTTTTTT[-/TT]GAGACAGAGTCTTGC | 197370 |
rs35187969 | snp | A/G | 0.45645 | 0.140991 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27239166 | TGAGCCACCGTGCCC[A/G]GCCCCGACACATTCC | 197370 |
rs35273685 | in-del | -/C | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27248542 | CAGCCTCCCAAGTAG[-/C]TGGGACTACAGGCAC | 197370 |
rs35322371 | in-del | -/CT | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27237634 | GGGGCAAGTCCCACC[-/CT]TCTCTGAAAGTGACA | 197370 |
rs35325451 | in-del | -/A | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27262068 | GGCCAACATGATGAA[-/A]CTCTGTCGCTACCAA | 197370 |
rs35413266 | in-del | -/T | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27231181 | AATGAGCAGATATTT[-/T]CCTGTAACATTTTTT | 197370 |
rs35510534 | in-del | -/CT | 0.391397 | 0.206172 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27237633 | TGGGGCAAGTCCCAC[-/CT]CTCTCTGAAAGTGAC | 197370 |
rs35526272 | in-del | -/C | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27261697 | AAAAAAGCAAACCCT[-/C]CCCCAACCCATCTGA | 197370 |
rs35696485 | in-del | -/A | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27231653 | AAAAAAAAAAAAAAA[-/A]TTGGCCTGAAGAGGG | 197370 |
rs35701419 | in-del | -/T | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27232155 | GCCACAAGCAGCAGC[-/T]CTCTGGCCACGAGTC | 197370 |
rs35788748 | snp | A/T | 0.45645 | 0.140991 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27239337 | TCTCTCCCCTGATCC[A/T]GGAGCCCTGGTGGAG | 197370 |
rs35817292 | in-del | -/G | | | downstream-variant-500B | NSMCE1 | GRCh38.p7 | 16:27224748 | ACTGGGGAGCTGGGG[-/G]AGGCCAAGGCTCACA | 197370 |
rs35966245 | snp | A/G | 0.432651 | 0.170701 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27227974 | ATTTTTAGTAGAGAC[A/G]GGGTTTCACCATGTT | 197370 |
rs35986918 | in-del | -/A | 0.435407 | 0.167703 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27244656 | ACATATGGCAGCTCC[-/A]CAGAAAGGTTTGAAC | 197370 |
rs36004076 | in-del | -/G | | | frameshift-variant | NSMCE1 | GRCh38.p7 | 16:27233100 | ACCAGGTTCAATATG[-/G]TTTGTGGAAGACGCA | 197370 |
rs55682705 | snp | C/T | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27228698 | ACAGCACCCCACATC[C/T]CCAGCCACCACCCTC | 197370 |
rs55724568 | snp | C/T | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27227788 | CTTTTCTTTTCTTTT[C/T]TTTTTTTTTTTTTTG | 197370 |
rs55756259 | snp | A/G | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27228813 | GCACCCCACATCCCC[A/G]GCCACCACCCTCTTC | 197370 |
rs55762579 | in-del | -/AAAAAAAAA | 0 | 0 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27260875 | AAAAAAAAAAAAAAA[-/AAAAAAAAA]GGTTGCGGGGGCTGG | 197370 |
rs55852443 | snp | A/G | 0.0333695 | 0.124785 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27238463 | CTGTGTCCAGCCGCC[A/G]CCCCAAGACAGGAGT | 197370 |
rs55946348 | snp | C/T | 0.046775 | 0.145601 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27264419 | ATAAAGCTAGAGTAA[C/T]GAGTACAGTGTGGTA | 197370 |
rs56007547 | snp | C/T | 0.43221 | 0.171171 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27230011 | CCTCAAAGACGACGA[C/T]AGCCCAGGTGATCTC | 197370 |
rs56262273 | snp | C/T | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27228697 | CACAGCACCCCACAT[C/T]CCCAGCCACCACCCT | 197370 |
rs56763897 | snp | C/T | 0.109108 | 0.206518 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27260610 | TAAAATCTACCTCTA[C/T]ATTATAAGAGTTCCT | 197370 |
rs57257601 | in-del | -/TGTA | 0.375399 | 0.216275 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27226251 | AAGGATACAGGTGTA[-/TGTA]CGAGGCCCGTAAGAG | 197370 |
rs57511400 | in-del | -/T | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27251207 | ATATATATATATATA[-/T]AAAACTCTGTAGAGT | 197370 |
rs57555475 | snp | C/T | 0.0788843 | 0.182262 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27236737 | AAAAAATGGACAATA[C/T]GATACATTCATGTGT | 197370 |
rs57771196 | snp | C/T | 0.0265275 | 0.112071 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27257398 | CCCTGATCAACACAG[C/T]ACCAGAGCGCCCTGG | 197370 |
rs57816168 | snp | A/C | 0.0337553 | 0.125452 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27234946 | CACTGAAGGCCCCAC[A/C]CACATGGCCTGCAAT | 197370 |
rs58108385 | in-del | -/AATAT/T | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27251191 | TATATATATATATAA[-/AATAT/T]ATATATATATATATA | 197370 |
rs58691360 | in-del | -/AA | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27251207 | TATATATATATATAT[-/AA]AAAACTCTGTAGAGT | 197370 |
rs58711921 | in-del | -/A | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27261393 | ATATTTGAAAAAAAA[-/A]GGAAATTAACTGCAA | 197370 |
rs58818873 | in-del | -/T | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27251209 | TATATATATATATAA[-/T]AACTCTGTAGAGTTC | 197370 |
rs58938880 | snp | C/G | 0.432651 | 0.170701 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27228846 | CCCTCCCCTCCAGAT[C/G]CATCATGGTACCCCA | 197370 |
rs59020602 | in-del | -/TAA | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27263701 | AACCTAAGTTTTTTT[-/TAA]AAAAAAGCATATGAT | 197370 |
rs59041824 | in-del | -/ACT | 0.391024 | 0.206427 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27236642 | TGTATTATTGTTTTC[-/ACT]ACTGTTTTTATGTAT | 197370 |
rs59275639 | snp | A/G | 0.0270145 | 0.113038 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27257407 | ACACAGCACCAGAGC[A/G]CCCTGGGAACAGGGA | 197370 |
rs59899931 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27226969 | TTTTCACCAACCCCA[A/G]CCAACGGGCATCAGC | 197370 |
rs60049751 | in-del | -/AG | 0.0638368 | 0.168964 | downstream-variant-500B | NSMCE1 | GRCh38.p7 | 16:27224989 | CTCGAGAACACAGAC[-/AG]GGGCTGCAGCAACTT | 197370 |
rs60159453 | in-del | -/T | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27256340 | AAGACTTTTCTTTTT[-/T]AATAAAAGAACATAA | 197370 |
rs60267018 | snp | A/G | 0.0759472 | 0.179459 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27254712 | TGCCTCAGCTTCCTG[A/G]GTAGCTAGGACCATA | 197370 |
rs61044565 | snp | A/T | 0.0341408 | 0.126114 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27245331 | AGCCAGCGGGGTCTG[A/T]GGTAATCCCACTGAA | 197370 |
rs61088115 | in-del | -/TTTTTT | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27254892 | TTTTTTTTTTTTTTT[-/TTTTTT]GATACATGGTCTCGC | 197370 |
rs61150536 | snp | A/G | 0.432504 | 0.170857 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27233606 | TGGATTCAACAGATC[A/G]TGAGTGGGGCTGAAA | 197370 |
rs61172255 | snp | A/C/G | 0.0845512 | 0.190893 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27264494 | AGAGAACTCAGAAAC[A/C/G]GAAAGGTATACATAT | 197370 |
rs61518319 | in-del | -/AA | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27251190 | TATATATATATATAT[-/AA]ATATATATATATATA | 197370 |
rs61528439 | in-del | -/AA | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27260874 | AAAAAAAAAAAAAAA[-/AA]GGTTGCGGGGGCTGG | 197370 |
rs61701543 | snp | C/T | 0.338976 | 0.23363 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27232808 | CATCATCTGGGTGAA[C/T]GGGGAGTGGGAGGCA | 197370 |
rs62028354 | snp | C/G | 0.406296 | 0.19512 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27228370 | TCATCCAAGTGCTGT[C/G]GGCAATGGGAGGATG | 197370 |
rs62028355 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27230779 | CAGGTGGCAGCTCCC[A/G]GATCCTCTGTCCACC | 197370 |
rs66463144 | in-del | -/TGTA | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27226252 | CCCAAGGATACAGGT[-/TGTA]GTACGAGGCCCGTAA | 197370 |
rs67224893 | snp | A/T | 0 | 0 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27251207 | ATATATATATATATA[A/T]AAAACTCTGTAGAGT | 197370 |
rs67952954 | in-del | -/CT/TC/TTC | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27238544 | TTCGCCTTTTTTCTT[-/CT/TC/TTC]TYTTTTTTTTTACAA | 197370 |
rs71272473 | in-del | -/TTC | 0.375 | 0.216506 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27238543 | CTTCGCCTTTTTTCT[-/TTC]TTTTTTTTTTTTACA | 197370 |
rs71377604 | snp | C/T | 0 | 0 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27248303 | AGTAGTATATTAGAG[C/T]TCCAGTTCCTCCATG | 197370 |
rs71387778 | in-del | -/A | 0.417521 | 0.185571 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27231637 | GCAAAACTCCATCTT[-/A]AAAAAAAAAAAAAAA | 197370 |
rs71387779 | in-del | -/GCCA | 0.454061 | 0.144427 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27239956 | ATTACCTTATTATGT[-/GCCA]GCCAGCACTATGCAT | 197370 |
rs71387781 | in-del | -/AAAAAAAAA | 0.5 | 0 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27260859 | GTGAGACCCTGTCTC[-/AAAAAAAAA]AAAAAAAAAAAAAAA | 197370 |
rs71387782 | in-del | -/AA | 0.488905 | 0.0736498 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27262244 | GTGAGACTTCATCTC[-/AA]AAAAAAAAAAAAAAA | 197370 |
rs71387783 | in-del | -/G | 0.5 | 0 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27262488 | ACAAAAAGAAGCAAT[-/G]GGGAAAAAGACTCCC | 197370 |
rs72782371 | snp | C/T | 0.0252325 | 0.109451 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27227589 | GGCAGGCAAATGACA[C/T]GGGACCCAGGACATG | 197370 |
rs72782373 | snp | A/G | 0.0252325 | 0.109451 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27242342 | AAAACCTATTGTTCT[A/G]AGATCTGTACACAGA | 197370 |
rs72782375 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27253846 | ACACAGGTCCCTAGC[A/G]CCATTCCGAAAGGCT | 197370 |
rs72782377 | snp | A/G | 0.0279526 | 0.114869 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27254499 | AACTTCCCCACCAAC[A/G]TGAAAGCTTACAGTC | 197370 |
rs72782383 | snp | A/G | 0.262985 | 0.249663 | intron-variant, upstream-variant-2KB | NSMCE1, FLJ21408 | GRCh38.p7 | 16:27267306 | TCAGTCATACCATTC[A/G]TGCGGGTGCTAACAC | 197370 |
rs73527513 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27260042 | TTCAGGAAGAAAGAA[A/G]GGGATACAAGTTGGA | 197370 |
rs73527521 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27264974 | GCAACAGAAATTTTA[C/T]AAAAAGAGGATGCAT | 197370 |
rs73527525 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27265271 | CTTGTGGGCTCAATC[A/G]ATCCTCTGACCTCAG | 197370 |
rs73527532 | snp | A/C | 0.00914312 | 0.0669923 | upstream-variant-2KB, intron-variant | NSMCE1, FLJ21408 | GRCh38.p7 | 16:27270517 | GTTGATAGGTTGGAT[A/C]AGAGAGGAAAGGAGT | 197370 |
rs74016031 | snp | A/C | 0.0310518 | 0.120672 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27225358 | GTCTACACCATCCTT[A/C]ACTGCTAACCCTCCC | 197370 |
rs74016035 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27227314 | CAACTGCAGTAGGGA[C/T]CCTCAGAGATCACTT | 197370 |
rs74016038 | snp | A/G | 0.432651 | 0.170701 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27228326 | TGTGCCCTGCACCGC[A/G]GCTGTTGCTGGTGCA | 197370 |
rs74016040 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27230270 | GAGTGACGTGTCCTT[A/G]GGGTGATATACCCAC | 197370 |
rs74364420 | snp | C/G | 0.5 | 0 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27247985 | TACTCTTTCACCTCA[C/G]TTCTTCCACTCAGCA | 197370 |
rs74431851 | snp | A/C | 0.0166325 | 0.0896639 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27263885 | CAATCACTTTAAAAA[A/C]CAAATTGACCCAATG | 197370 |
rs74465456 | snp | G/T | 0 | 0 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27248405 | CTGCGGTTTTAGTTT[G/T]CTTTTTTTTTTTTTT | 197370 |
rs74575790 | snp | A/C | 0 | 0 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27260860 | TGAGACCCTGTCTCA[A/C]AAAAAAAAAAAAAAA | 197370 |
rs74809760 | snp | C/T | 0.000497314 | 0.015761 | synonymous-codon | NSMCE1 | GRCh38.p7 | 16:27226771 | CACCGCGTCGGGGTA[C/T]GTCTCCCGGATGTAT | 197370 |
rs74815164 | snp | C/T | 0.0513262 | 0.151752 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27246489 | TAGGTAAAAATGGGA[C/T]GAAGAGTGGGATTAT | 197370 |
rs74938720 | snp | A/G | 0.040671 | 0.13668 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27232106 | CCCCAACCCAGACGC[A/G]AGCCTTCCTGAAAAG | 197370 |
rs74992394 | snp | C/G | 0.0670745 | 0.170406 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27238524 | ATGTCCCTCCCTAAC[C/G]AGACCTTCGCCTTTT | 197370 |
rs75278489 | snp | A/C | 0.0103295 | 0.0711199 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27240682 | AGCACTGAACAAAAC[A/C]GGACACTTCTCCCCT | 197370 |
rs75509025 | snp | A/G | 0.0532157 | 0.154195 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27227359 | TTACAGATGGAGCTG[A/G]AAGGAGTCTGGAGAG | 197370 |
rs75630104 | snp | C/T | 0.101301 | 0.200969 | intron-variant | NSMCE1, FLJ21408 | GRCh38.p7 | 16:27268497 | CATCCCAGTCCGCTG[C/T]TTTCTGCGGCCCCTG | 197370 |
rs75641118 | snp | A/G | 0.0513262 | 0.151752 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27254002 | GTGATTTGATAAACT[A/G]GACAAACACCCTGGG | 197370 |
rs75675335 | snp | A/C | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27251415 | ATATGGTGAATTACA[A/C]TGATTTTCAAATATT | 197370 |
rs75688051 | snp | A/T | 0.5 | 0 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27231653 | AAAAAAAAAAAAAAA[A/T]TTGGCCTGAAGAGGG | 197370 |
rs75738267 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27259812 | CAGATGACTTCTAAA[A/G]AGCAACAAGTAGACT | 197370 |
rs75884365 | snp | A/G | 0.5 | 0 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27226190 | AGCTTTCAAAAAAAA[A/G]GTGCACTTTGTCCCA | 197370 |
rs75975475 | snp | C/G | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27237640 | AAGTCCCACCTCTCT[C/G]AAAGTGACAATTCAC | 197370 |
rs76168799 | snp | A/T | 0.5 | 0 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27245736 | TACTTTTCATACTCA[A/T]TTTTTGCCACTTTTC | 197370 |
rs76184466 | snp | A/C | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27235341 | GGGGTGACCAGGGGG[A/C]CTCATCAAAAAAATG | 197370 |
rs76248670 | snp | C/T | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27238546 | TCGCCTTTTTTCTTT[C/T]TTTTTTTTTACAATT | 197370 |
rs76255710 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27234459 | AGCTCAGCCAACATG[C/G]TGGGCCCTCAGAAGT | 197370 |
rs76308256 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27227701 | CGCCTGCAAGTCACC[C/T]GAGTGCTCAACTGCC | 197370 |
rs76388641 | snp | G/T | 0.0509478 | 0.151255 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27251472 | GGATAAACCCTACTT[G/T]GTTATGTCGTACCAT | 197370 |
rs76471124 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27255792 | TCTGGGATCAGGCTT[C/T]GAACTCTAACATGCT | 197370 |
rs76595415 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27234320 | TGCGTGTTGGTTAAC[A/G]TGTCGCTGGCTCTCC | 197370 |
rs76744294 | snp | A/G | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27256238 | GAATAAAAACCAAAC[A/G]CCTGCATTCCCATTC | 197370 |
rs76780921 | snp | C/T | 0.0517044 | 0.152246 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27243534 | CCCACCACCTCTAAG[C/T]CAGACCTGCAGGAAG | 197370 |
rs76802777 | snp | C/T | 0.0509478 | 0.151255 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27259526 | GAACATGGTGTTGCC[C/T]AGCTGTGTTTTAGGG | 197370 |
rs76981593 | snp | C/T | 0.040671 | 0.13668 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27233500 | ACGCAGGTGTGTGCT[C/T]AGCTCAGCACCTGCT | 197370 |
rs77056450 | snp | A/T | 0.5 | 0 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27245735 | TTACTTTTCATACTC[A/T]TTTTTTGCCACTTTT | 197370 |
rs77130343 | snp | A/G | 0.000298517 | 0.0122135 | synonymous-codon | NSMCE1 | GRCh38.p7 | 16:27226762 | GCAGATCTTCACCGC[A/G]TCGGGGTACGTCTCC | 197370 |
rs77183237 | snp | A/G | 0.0517044 | 0.152246 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27247560 | TCCTATCCCTCCTCT[A/G]TGCCATCCCCATGCA | 197370 |
rs77185997 | snp | G/T | 0.5 | 0 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27234646 | TTTGACTCTGTAATG[G/T]TTTTTTTCCAGGGAA | 197370 |
rs77387105 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27249673 | GTCTTGATAGGACAG[A/C]CATACAGTAAGTCTT | 197370 |
rs77484393 | snp | C/T | 0.00108329 | 0.023248 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27235134 | GCCTGGGCCCTGTTC[C/T]AGCTCCTCAAAAATG | 197370 |
rs77506915 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27233264 | TCACAGGCAGAACTG[C/T]ACACTGGCATGGTAT | 197370 |
rs77518320 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27242987 | CAGATTGCACTGAGC[A/G]AACTGAAAATGGACA | 197370 |
rs77590685 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | NSMCE1, FLJ21408 | GRCh38.p7 | 16:27268176 | ACCTTTCCAAACTCC[A/G]AGAACTCCTCGATTT | 197370 |
rs77646137 | snp | C/T | 0.0433465 | 0.140692 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27239585 | AACTGAAGAAAAAGA[C/T]ACAACCTTCAGTAAA | 197370 |
rs77754207 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27239483 | CGTATGGTGAGATTC[C/T]GAGACAACTACTTTC | 197370 |
rs77890842 | snp | C/T | 0.031825 | 0.122064 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27257342 | CTCAGCTCAGGAGTA[C/T]CGGTTAACAAGTTAC | 197370 |
rs77983756 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | NSMCE1, FLJ21408 | GRCh38.p7 | 16:27270252 | AAAGATGATTTTCAA[C/T]ATACTGGAGGATTTG | 197370 |
rs78040047 | in-del | -/A | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27236962 | AAGTTAAAAAAAAAA[-/A]ACAACAGAAGATCAT | 197370 |
rs78161275 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27248031 | ATTCATATTCTAGCA[C/T]GTAGGAAGAGCTCAC | 197370 |
rs78275880 | snp | G/T | 0.0130921 | 0.0798413 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27259584 | TGTAGAGGAAAGAAA[G/T]GGGAGGCAAAGAGTC | 197370 |
rs78334888 | snp | A/G | 0.0509478 | 0.151255 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27257828 | TCCCACTTACTAGGC[A/G]TGTGAGATTGAGCAA | 197370 |
rs78525963 | in-del | -/AA | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27247938 | TCTCAAAAAAAAAAA[-/AA]CAAAAAACAAAACAA | 197370 |
rs78538629 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27251638 | GTCTCATAGAATTAG[C/T]TGTAACATATTCTCT | 197370 |
rs78629678 | snp | G/T | 0.0252325 | 0.109451 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27244302 | GGCTGGTATGAAGGC[G/T]GCTGACTGCAGTCGC | 197370 |
rs78963714 | snp | A/G | 0.000828555 | 0.0203369 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27234165 | AAGCCCACCCAATGG[A/G]CAATGGGGATTACTC | 197370 |
rs79108527 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant, upstream-variant-2KB | NSMCE1, FLJ21408 | GRCh38.p7 | 16:27266959 | AAAATGGGAGAAAAA[C/T]TGGTTTTAATCCCAT | 197370 |
rs79230698 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27257241 | TATCCACAGGGCTAA[A/T]TGTCAGGTTTACTTG | 197370 |
rs79423904 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27231335 | GGTCATAACCCCTAC[C/T]CTTAAAAAACTTGGC | 197370 |
rs79513641 | snp | A/C | 0.0248432 | 0.108648 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27256621 | GCACACAACTCAACA[A/C]TATCTGCCAATGCTA | 197370 |
rs79534971 | snp | A/G | 0.0509478 | 0.151255 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27256757 | CCAGTGGCCCCGTAA[A/G]ATGCCCCAAATGCCT | 197370 |
rs79568779 | snp | C/T | 0.0509478 | 0.151255 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27251465 | AAAATCAGGATAAAC[C/T]CTACTTGGTTATGTC | 197370 |
rs79634661 | snp | A/C | 0.5 | 0 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27247927 | GCAAGACTCTGTCTC[A/C]AAAAAAAAAAAACAA | 197370 |
rs79739100 | snp | A/G | 0.040671 | 0.13668 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27231811 | CCGGGGCCTGAACTC[A/G]GCCCTGCCACTCTCA | 197370 |
rs79814007 | snp | A/C | 0.0509478 | 0.151255 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27256898 | TTTTTTCAAATAAAA[A/C]AATAGAGAGGGTCTT | 197370 |
rs79879658 | snp | C/G | 0.0189856 | 0.0955633 | downstream-variant-500B | NSMCE1 | GRCh38.p7 | 16:27224842 | GGCTGCCCTGGGCAA[C/G]GACAGTGAGCTGTTC | 197370 |
rs79894144 | snp | A/C | 0.5 | 0 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27232989 | CAGGCTGGAAAAACC[A/C]TGAGACAGTACCTCA | 197370 |
rs79939181 | snp | A/G | 0.0513262 | 0.151752 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27244236 | GTTCACACTTTATCC[A/G]TGGAGGACTCAATTT | 197370 |
rs80066181 | snp | A/C | 0.0154538 | 0.0865337 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27229307 | CAGCTGTCATAAAGC[A/C]ATGTTTCCTTTCCAT | 197370 |
rs80184721 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27240493 | CCCAGCATCCATCAT[C/T]CCCTTGGCCCAGCCC | 197370 |
rs80266881 | snp | C/G | 0.0524604 | 0.153226 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27240718 | GAAGGGTTGGCTCAA[C/G]TCATCTTGAGAGATT | 197370 |
rs80292790 | snp | A/G | 0.0402882 | 0.136092 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27238159 | TGGCATGGGGCCAGA[A/G]GCAGAGGTGTGGGCT | 197370 |
rs80321706 | snp | A/G | 0.0509478 | 0.151255 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27256098 | TGTCCCTTCACCTGT[A/G]TACTTGCTCCCTGTG | 197370 |
rs80323726 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27252385 | GGAATGGCCAGGCAC[A/G]GTGGCTAAATAAATA | 197370 |
rs80355878 | snp | A/G | 0.0232847 | 0.105357 | upstream-variant-2KB, intron-variant | NSMCE1, FLJ21408 | GRCh38.p7 | 16:27269578 | TTGGTGAGATTTACA[A/G]GAGATAATAACACCT | 197370 |
rs111241597 | snp | C/T | 0.00119737 | 0.0244387 | downstream-variant-500B | NSMCE1 | GRCh38.p7 | 16:27224666 | GGGAGGGAGAGCACG[C/T]ATCCCGCCCAAACGC | 197370 |
rs111284469 | in-del | -/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | NSMCE1, FLJ21408 | GRCh38.p7 | 16:27267735 | GTGTAAATATATGCA[-/T]TTTTTTTTTTGAGAC | 197370 |
rs111333647 | snp | A/G | 0.00185744 | 0.0304182 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27241928 | AAGTCTAGACCAGAA[A/G]TCAGATGTCTGGCCA | 197370 |
rs111576311 | snp | C/G | 0.00953873 | 0.0683987 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27254441 | AAAAACACTTTCAGT[C/G]TTAGTACCAAGGCAT | 197370 |
rs111860116 | snp | C/T | 0.5 | 0 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27244646 | GAGCATCGCCACATA[C/T]GGCAGCTCCACAGAA | 197370 |
rs111906617 | snp | G/T | 0.0170251 | 0.090679 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27238151 | TGGCGTGGTGGCATG[G/T]GGCCAGAAGCAGAGG | 197370 |
rs112037776 | snp | C/T | 0 | 0 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27252598 | GACCAGCCTAGGCCA[C/T]AGAAGAAGACCCCCG | 197370 |
rs112181843 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27226491 | GTAAGCGAGGGCCCT[C/T]GGACCCCAACAGCAG | 197370 |
rs112197160 | snp | C/T | 0.5 | 0 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27239447 | AGCCCATGGTCATGA[C/T]AAAGAGTGCGGAATA | 197370 |
rs112275621 | snp | A/G | 0.0341408 | 0.126114 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27254752 | CAGCACACCTGGCTA[A/G]TTTTTTGTACTTTTG | 197370 |
rs112367080 | snp | A/G | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27231368 | GTGGCCGGGCACGCT[A/G]GCTCACGCCTGTCAT | 197370 |
rs112385375 | snp | A/C | 0 | 0 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27239819 | ACCTCTAAACCTCTA[A/C]ACACAGTGCTATCTG | 197370 |
rs112396887 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27252968 | TGAACGACAGGATTT[A/G]AAGAGCTTCGGGTTA | 197370 |
rs112741453 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27261886 | GGTTTATTCCAGCAA[G/T]GGTTTCACATCTAAA | 197370 |
rs112826019 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27237557 | TGCAAGAGGCCCAGA[C/T]ATCAAAAAGCCTCGT | 197370 |
rs112838979 | snp | A/C | 0.0174175 | 0.0916809 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27245217 | TGATGTCCCTTATAA[A/C]ACAGAAAGCTGAGAC | 197370 |
rs112921969 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27251309 | CTATAAAAAACTTTC[C/T]GCTACATCACACCAG | 197370 |
rs112922179 | snp | A/C | 0.0154538 | 0.0865337 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27227067 | CTCCCTGACACCCGC[A/C]TTTTCTCAGCATCTG | 197370 |
rs112927726 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27257060 | AGGCACTGTCTCTGC[A/G]CCACTGTCTTGTACA | 197370 |
rs113002199 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27236357 | GCTGGAGTGCAGTAG[A/C/G]ACAGTCTTGGCTCAC | 197370 |
rs113010419 | snp | A/G | 0 | 0 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27245550 | GCAGACATGAAGAAC[A/G]GGCAGGACTTGGACA | 197370 |
rs113016759 | in-del | -/AG | 0.00159617 | 0.0282053 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27232287 | TGAGCTGTTGAAAAC[-/AG]GGGTGCCTTTTGTGG | 197370 |
rs113123539 | snp | A/G | 0 | 0 | downstream-variant-500B | NSMCE1 | GRCh38.p7 | 16:27224990 | CTCGAGAACACAGAC[A/G]GGCTGCAGCAACTTC | 197370 |
rs113336335 | snp | C/G | 0.0581099 | 0.160244 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27250358 | CTTTCACCATTAAGA[C/G]TGATGTTAGCTGTAG | 197370 |
rs113336339 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27226264 | AGGTGTACGAGGCCC[A/G]TAAGAGCAATTGCAA | 197370 |
rs113427390 | snp | A/C/T | 0 | 0 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27252654 | CCGGGCGCGGTGGCT[A/C/T]ATGCCTGTAATCCCA | 197370 |
rs113457896 | snp | A/G | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27233450 | AGAGAGAGACACGGC[A/G]GGCAGGAACCGCTGG | 197370 |
rs113466442 | snp | A/C | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27251180 | TATATATATATATAT[A/C]TATATATATAAATAT | 197370 |
rs113611873 | snp | A/G | 0.5 | 0 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27255320 | CGGAGATGGTTCTCA[A/G]ACCTAAAACTGTCTC | 197370 |
rs113642718 | snp | C/G | 0.119281 | 0.213102 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27231388 | ACGCCTGTCATCCCA[C/G]CACTTTGGGAGGCTG | 197370 |
rs113807948 | snp | G/T | 0.5 | 0 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27247035 | TCTACAAATAGCACA[G/T]GTGGCTACTGAGCAC | 197370 |
rs113971682 | snp | C/T | 0.0341408 | 0.126114 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27260973 | GGAGGTGGAGACCAG[C/T]CTGGTTAACATGGTG | 197370 |
rs114031262 | snp | C/T | 0.0513262 | 0.151752 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27244902 | ACGAACCGAGGAAGA[C/T]GTGTGGTACAAGTGG | 197370 |
rs114066493 | snp | A/T | 0.0178098 | 0.0926698 | intron-variant, upstream-variant-2KB | NSMCE1, FLJ21408 | GRCh38.p7 | 16:27267728 | CCCAACAGTGTAAAT[A/T]TATGCATTTTTTTTT | 197370 |
rs114070664 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27245366 | TTCCCAGTACTTCCA[C/T]GCATCAGCACATAAC | 197370 |
rs114158782 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27250086 | GCATATAGAGAAACA[A/G]TTGGTATTTGGATAT | 197370 |
rs114205721 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant, upstream-variant-2KB | NSMCE1, FLJ21408 | GRCh38.p7 | 16:27266407 | AAGAGACTGTAGGGA[A/G]AATGGTGGGATTAGC | 197370 |
rs114232758 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27265598 | GGAGATATGTTTTTA[C/T]AGAAGCACCTTGTAA | 197370 |
rs114307515 | snp | C/T | 0.0437281 | 0.141251 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27236996 | GGTGACAATGGAGGA[C/T]GTGGCCGTGTGAAAG | 197370 |
rs114358963 | snp | A/C/G | 0.0115144 | 0.0749975 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27246209 | GTATTTCAGCGACCT[A/C/G]GTTTTTGCCCAAACA | 197370 |
rs114502290 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27257300 | TAGAAAGATGGGCCC[A/G]TGTAAGATTGTGAAG | 197370 |
rs114608837 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27232349 | TTCAGCAGGACTAGA[C/T]GTGGGGGTGGGGGCA | 197370 |
rs114720367 | snp | C/G | 0.0178098 | 0.0926698 | intron-variant, upstream-variant-2KB | NSMCE1, FLJ21408 | GRCh38.p7 | 16:27268023 | GCTGGAATTATAGCC[C/G]TGGGCCACCGCGACC | 197370 |
rs114723873 | snp | C/T | 0.0513262 | 0.151752 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27245427 | GCATTCCCAAACACA[C/T]GATGTGTGTGCTTAG | 197370 |
rs114900634 | snp | C/T | 0.0509478 | 0.151255 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27259662 | ACCGAGGCTTGGCAG[C/T]GGGGACAAATGATAC | 197370 |
rs114919067 | snp | C/G | 0.0513262 | 0.151752 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27243785 | TCTCCCCAGTAGCTG[C/G]GACTACAAGCACGAG | 197370 |
rs115135259 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27259862 | GCAACAATGGAAGCC[A/G]GTCACAGTGGAAACA | 197370 |
rs115185662 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27231928 | CATGACATACGGGAA[C/T]GCGCCCAGCAGATCC | 197370 |
rs115190707 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant, utr-variant-5-prime | NSMCE1 | GRCh38.p7 | 16:27241695 | TGCTGGGAAGAGCCG[A/G]GTGGAAGGAGAGTGG | 197370 |
rs115317971 | snp | A/G | 0.0513262 | 0.151752 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27246042 | GTACAGGAGTCCAGC[A/G]TGAGACGACGAAGCA | 197370 |
rs115358507 | snp | A/C/T | 0.0182019 | 0.0936463 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27265050 | TCAGACAAATGATTA[A/C/T]GAAAACCACAGTGAA | 197370 |
rs115508528 | snp | C/G | 0.021333 | 0.101051 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27235980 | GAAGAGGCTGAGACG[C/G]AGAGAGGTGAACTGA | 197370 |
rs115594485 | snp | A/T | 0.0517044 | 0.152246 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27247183 | TCCCATAATCCAAAC[A/T]TGTCATGGGAGGGGC | 197370 |
rs115613040 | snp | A/G | 0.0298908 | 0.118541 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27231656 | AAAAAAAAAAAAATT[A/G]GCCTGAAGAGGGGCT | 197370 |
rs115621926 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27240665 | CCTCCAGGCAAGTGA[C/T]AAGCACTGAACAAAA | 197370 |
rs115640206 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27236137 | ACCCACACTATTGCC[A/G]GGGGCTCAGCTGAGG | 197370 |
rs115641630 | snp | G/T | 0.0178098 | 0.0926698 | intron-variant, upstream-variant-2KB | NSMCE1, FLJ21408 | GRCh38.p7 | 16:27267123 | TAAAAAAACCTTTTC[G/T]AAGGCTTTTGAAGCA | 197370 |
rs115819171 | snp | G/T | 0.0170251 | 0.090679 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27237254 | GCCTCGGCGGCTGGA[G/T]AGCAGGCATCAGGAG | 197370 |
rs116033396 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27249509 | GATATCCAATTATTC[C/T]AGCACTCATTTTGGA | 197370 |
rs116056629 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27230459 | TTCCTCCAGAGTGCC[A/G]CAGACCTCAAGGCAA | 197370 |
rs116202007 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27256551 | CATCATACAATTACT[C/T]ATCCATCACCTTTGT | 197370 |
rs116206016 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27260049 | AGAAAGAAAGGGATA[C/T]AAGTTGGAAGGTCTA | 197370 |
rs116278536 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27226329 | TGAAAGACACATCAA[C/T]GTCCACGCTGGTTCA | 197370 |
rs116279309 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27247150 | TGTGTCCACCCAAAT[C/T]TCATCTTGAATTGTA | 197370 |
rs116364541 | snp | C/G | 0.0283406 | 0.115616 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27249626 | TTTTTTTCCCTTCAT[C/G]TGTTTGTCCATCATG | 197370 |
rs116479181 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant, upstream-variant-2KB | NSMCE1, FLJ21408 | GRCh38.p7 | 16:27266668 | AATTAAAACAGTTTA[C/T]TGGCTTTAAATGTAC | 197370 |
rs116513103 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27264454 | TACAGAGATAGACAA[A/G]TAAGACCAATCAATG | 197370 |
rs116592210 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27249221 | TATTTGCAAATATTT[C/T]CTCTTAGTATTTTGC | 197370 |
rs116703068 | snp | A/G | 0.0174175 | 0.0916809 | upstream-variant-2KB, intron-variant | NSMCE1, FLJ21408 | GRCh38.p7 | 16:27268891 | TGGTGGTTCCGCCTC[A/G]TGGGTTAGATCCCAA | 197370 |
rs116766391 | snp | A/G | 0.0232847 | 0.105357 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27257920 | CTGCAGAACTGCTAC[A/G]AAGATTAGATGGGTT | 197370 |
rs116865075 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27243444 | AAACAGCCAATGGGC[C/T]GCAGCCAATGGCCAG | 197370 |
rs116942558 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant, upstream-variant-2KB | NSMCE1, FLJ21408 | GRCh38.p7 | 16:27267315 | CCATTCGTGCGGGTG[C/T]TAACACAATTCTAGT | 197370 |
rs116944457 | snp | A/G | 0.0437281 | 0.141251 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27258696 | CCAAAGGCTTGCCAA[A/G]CACCTGGCACATAAG | 197370 |
rs116991841 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27264518 | TACATATATGGATAC[C/T]TGATGGCGGATGAAA | 197370 |
rs117192464 | snp | A/G | 0.0165278 | 0.0893908 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27252552 | TTTTGGAAGGCTGAC[A/G]CAGGATGATCACTTG | 197370 |
rs117219610 | snp | C/T | 0.0283884 | 0.115708 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27235142 | CCTGTTCCAGCTCCT[C/T]AAAAATGCCACTAGA | 197370 |
rs117282203 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27263675 | TCTAATAAACCTTCA[C/T]GTGTGCTGCCAAACC | 197370 |
rs117334127 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27258073 | ATTGAGCAGAGGCCC[C/T]GTTTTCTCACCATAA | 197370 |
rs117491131 | snp | A/G | 0.00676609 | 0.0577691 | downstream-variant-500B | NSMCE1 | GRCh38.p7 | 16:27224897 | TGGCTTCACCTGCTG[A/G]AGCCCAAACCCAGGG | 197370 |
rs117492133 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27231704 | GGTCAGTTATAACCT[A/G]AGTAGCCCTAGAACA | 197370 |
rs117564667 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27257829 | CCCACTTACTAGGCG[C/T]GTGAGATTGAGCAAC | 197370 |
rs117635961 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | NSMCE1 | GRCh38.p7 | 16:27225086 | ACCTGAAACACGGAC[A/G]CCTTTCTTCCAAGAA | 197370 |
rs117649305 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27251541 | GGTTTAGCACGTTAA[C/T]GTCTACGCTCATGAG | 197370 |
rs117657877 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27228389 | AATGGGAGGATGTGA[C/T]CAGCCCCCAGGCTGT | 197370 |
rs117688077 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27259587 | AGAGGAAAGAAATGG[C/G]AGGCAAAGAGTCCAG | 197370 |
rs117736837 | snp | A/T | 0.0475351 | 0.146656 | upstream-variant-2KB, intron-variant | NSMCE1, FLJ21408 | GRCh38.p7 | 16:27270495 | GAGGTGCTGGGGATT[A/T]GAGAGTGTTGATAGG | 197370 |
rs117739208 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27245456 | AGGGGAGCGTGAAGC[A/G]CACAGAAATCCTGGC | 197370 |
rs117765468 | snp | A/C | 0.00355621 | 0.0420173 | missense, utr-variant-5-prime | NSMCE1 | GRCh38.p7 | 16:27235250 | CAAGGACTCCAAGAC[A/C]CTGTTAATGTTGTTG | 197370 |
rs118119491 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27243592 | AGAAGCCAAAACTAA[C/T]CCACAATCATGGCCC | 197370 |
rs118179628 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27239982 | TGCATTCACATGGTT[C/T]ATTTCATCATGACAA | 197370 |
rs137924829 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27227031 | AACTGAGGCAAAGAC[C/T]CTAAAGACATGGAGG | 197370 |
rs138108237 | snp | C/G | 0.0298908 | 0.118541 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27238226 | CGTGAGCCTCTCCCC[C/G]ACTTCTCATCTCTAA | 197370 |
rs138235295 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27256084 | TTGCCTTTTTTTTGT[A/G]TCCCTTCACCTGTGT | 197370 |
rs138284482 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27262845 | TTGCAAACTATTTAC[C/G]AGAGAAAATCAAACA | 197370 |
rs138432799 | snp | A/C | 0.0236746 | 0.106192 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27230693 | AGGCCAGGCAGTCAA[A/C]AAGAAGCCTCTCTAG | 197370 |
rs138433907 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27244921 | TGGTACAAGTGGTGA[C/G]CATGCTTTGTGAATT | 197370 |
rs138444984 | snp | A/G | 0.0232847 | 0.105357 | upstream-variant-2KB, intron-variant | NSMCE1, FLJ21408 | GRCh38.p7 | 16:27269670 | CTGTTATCTTACCTA[A/G]GGATTGTGAGAAAGC | 197370 |
rs138495086 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27251958 | TCTCATCTCCATCTC[C/T]TCAACGCAGGGAGGC | 197370 |
rs138677174 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27249034 | GGAGTTTTGTCATGT[G/T]GCCCAGGCTGGCCTC | 197370 |
rs138747211 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27233905 | TGGAGCAGCCAGGCA[A/G]GAACGCCTGTTACTA | 197370 |
rs138787964 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27243862 | CGCAATGTTGCCCAG[A/G]CTGGTCTCAAACTCC | 197370 |
rs138847987 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27238777 | GGGCCAGCTGCTCTG[G/T]CCATGAGGTGATGCC | 197370 |
rs138864301 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27257633 | CACATCAGAAGCAAC[A/G]TCCTGGGTCTTGTAC | 197370 |
rs139106787 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27246963 | TTATATCTGCAAAGT[C/T]AAAACTCCTAGATCT | 197370 |
rs139155637 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27231530 | TGATTCCAGCTACTT[A/G]GGAGGCTGAGGCAGG | 197370 |
rs139204312 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27226263 | CAGGTGTACGAGGCC[C/T]GTAAGAGCAATTGCA | 197370 |
rs139405623 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27264132 | ACTTTGGGAGGCTGA[C/T]GTGGGCAGATTGCTT | 197370 |
rs139462736 | snp | A/C/T | 0.0127027 | 0.0787217 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27252833 | CTGAGGCAGGAGAAT[A/C/T]GCTTGAACCTGGGAG | 197370 |
rs139564173 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27259752 | CTAGGCTCATCCTAA[C/T]AAAACCACACAATAC | 197370 |
rs139689293 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27245806 | AGGCAGACCGGCTCT[G/T]ACAGTGGTATGCTGA | 197370 |
rs139704611 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27243200 | TAAAAATTACAAACA[C/T]TATAGTGCAAACAAA | 197370 |
rs139797620 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27253030 | CAAGTAGAGAGGGCA[A/C/T]GGAAACTCCATGCCA | 197370 |
rs139823241 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27239512 | TCAGTCTTAGAAATA[C/T]CACTTTGAAGACTTA | 197370 |
rs139893408 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27227557 | ACAGGAGAAAGGCAG[C/T]ACTGAGGGAGACCCA | 197370 |
rs140235637 | snp | C/T | 0 | 0 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27237971 | TCCTTCCACACGCTT[C/T]CTGCATCAGGGTCAT | 197370 |
rs140437550 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27254911 | TTGATACATGGTCTC[A/G]CTCTGTCGCCCAAGC | 197370 |
rs140583026 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27260134 | AAGTTAACTGTATAA[A/G]ACAGTAAAAATCAGA | 197370 |
rs140792289 | snp | C/T | 0.000132641 | 0.00814267 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27232998 | AAAACCATGAGACAG[C/T]ACCTCAATCAGCCAC | 197370 |
rs140850956 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27234939 | TGAAAACCACTGAAG[A/G]CCCCACCCACATGGC | 197370 |
rs140866881 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27243685 | AGATGGGGTCTCGCT[C/T]TGTCATCTAGGCTGG | 197370 |
rs140934115 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27237456 | TGCTGGCGTGGGAGC[C/T]GAGCTGTTCCGTACC | 197370 |
rs140941458 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27228296 | CAGTGGAGGGAGGCC[A/G]GGGCACCAGGTGCTT | 197370 |
rs140975413 | snp | G/T | 0.0517044 | 0.152246 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27247863 | ACCTGGGAGGTGGAG[G/T]TTGCAGTGAGCGGAG | 197370 |
rs141050310 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27232787 | CTGGCTGTGGCATCC[C/T]GAACACATCATCTGG | 197370 |
rs141143621 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27226863 | CACAGGAGGTGGCCA[A/C]CCTCAGCCAGGCCCT | 197370 |
rs141212259 | snp | G/T | 0.00159617 | 0.0282053 | utr-variant-5-prime, intron-variant, upstream-variant-2KB, missense | NSMCE1, FLJ21408 | GRCh38.p7 | 16:27268748 | CGCTAGCGGATACGG[G/T]CGCAAGGTGGACTCT | 197370 |
rs141218664 | snp | A/C | 0.0193772 | 0.0965046 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27261151 | CAGCCTGGGTGACAA[A/C]GCAAGACTCCGTCTC | 197370 |
rs141340104 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27244332 | CTCTGACAGGCGCAC[A/G]CCCTTCCCTTTCCCC | 197370 |
rs141514041 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27262680 | TCCTGGACACAGGAA[C/G]GGGCAAAGATCTCAC | 197370 |
rs141729013 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27231512 | TGTGATGGCGCATGC[C/T]TGTGATTCCAGCTAC | 197370 |
rs141744202 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27230131 | CAGCTCCCATGAGCC[A/G]CGCTTGCTCTCAGAG | 197370 |
rs141756098 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27226516 | CAGCAGAACCAGGGA[A/G]GAGGGCGGCAGTGCG | 197370 |
rs141758493 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27234470 | CATGCTGGGCCCTCA[A/G]AAGTTTCAGAACTCC | 197370 |
rs141814806 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27234127 | TGCCACTGCTAATGA[C/T]GGAGACAGAACTTTC | 197370 |
rs141865783 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27239844 | TATCTGTGTTCTCTC[G/T]ACTTGGAAGAGGCAG | 197370 |
rs141891851 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27232479 | TCACTGCTGACAAAA[A/G/T]CAACAGTGGTAATGT | 197370 |
rs142195944 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27247479 | GTCTTTATTAGCAGC[A/G]CGAGAACGGACTAAT | 197370 |
rs142353916 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27231012 | CAAGCCATGCACAAT[A/G]GTGGCAGCATGTGCT | 197370 |
rs142426211 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27237203 | GTGGGTGGAACATGG[A/G]TGTGGTGAGATCGTA | 197370 |
rs142527660 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27243419 | CATTCTTCTGAGAGA[C/T]TGAACATACAAACAG | 197370 |
rs142540551 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27252645 | AAAACTTAGCCGGGC[A/G]CGGTGGCTCATGCCT | 197370 |
rs142541255 | snp | A/G | 0.00835141 | 0.0640778 | upstream-variant-2KB, intron-variant | NSMCE1, FLJ21408 | GRCh38.p7 | 16:27269972 | GTGTGGTGATTAAAA[A/G]CTTCAGCTTTGGAGC | 197370 |
rs142686377 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27258802 | GTTGCCCAGGCTGGA[A/G]TGCAGTGGCGTGATC | 197370 |
rs142734098 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27263482 | CTCACTTATAAGTGG[A/G]AGTTAAATGATGAAA | 197370 |
rs142804877 | in-del | -/TTTTCTTTTT | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27227779 | CTCCCGTTTCTTTTC[-/TTTTCTTTTT]TTTTTTTTTTTTTTG | 197370 |
rs142932432 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27252067 | CTCACTCCCACTATC[A/G]CTTGTGGCAGAAGAA | 197370 |
rs143023229 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27256088 | CTTTTTTTTGTGTCC[C/G]TTCACCTGTGTACTT | 197370 |
rs143145402 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27238299 | ACCCTCTTCCCTCCC[A/G]CTTCTCTACCACCAC | 197370 |
rs143220668 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27243223 | CAAACAAACAATGCC[A/T]GTAAGTTATATACCA | 197370 |
rs143394527 | snp | A/G | | | upstream-variant-2KB, intron-variant | NSMCE1, FLJ21408 | GRCh38.p7 | 16:27270567 | TGAGTCAGATCCTGG[A/G]TTAGGACCATAGGAC | 197370 |
rs143427040 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27227642 | TTTCTCCACAGTCAG[C/T]TCATGCATCGGATAT | 197370 |
rs143460625 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27264432 | AACGAGTACAGTGTG[A/G]TAATGGTACAGAGAT | 197370 |
rs143827850 | snp | G/T | 0.0130921 | 0.0798413 | upstream-variant-2KB, intron-variant | NSMCE1, FLJ21408 | GRCh38.p7 | 16:27269560 | AGTTCTTGCAAAATA[G/T]TGTTGGTGAGATTTA | 197370 |
rs143947490 | snp | C/G | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27258564 | GGCAAATACAGCAGG[C/G]AAACATTTTTAGCTA | 197370 |
rs144241419 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE1, FLJ21408 | GRCh38.p7 | 16:27268464 | TTTTTAGATGTCTGC[A/G]TGTGTGTTGCGGGAG | 197370 |
rs144246772 | snp | C/T | 0.0543475 | 0.155628 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27252897 | GCACTCCAGCCTGGG[C/T]GACAAGAGCAAAACT | 197370 |
rs144249333 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27245455 | TAGGGGAGCGTGAAG[C/T]GCACAGAAATCCTGG | 197370 |
rs144442437 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27246413 | GAGTATAGAACTGTA[C/T]CTCACAGCAGTCTGG | 197370 |
rs144660861 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27232318 | GAAAAAGAACTGAAA[C/T]ATTTGTTCTGCTCCA | 197370 |
rs144879925 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27228868 | GGTACCCCACATCCC[C/T]GGCCACCGCCCTCTT | 197370 |
rs144973752 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27232892 | GCAGATAAGGGATCC[A/G]AGAAGGCCGGGCTCC | 197370 |
rs144983104 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27253393 | TCTAGAGAACTGGAG[C/T]AGTGTTAGAAAAGAT | 197370 |
rs145162086 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27262105 | AAAAATTGGTTGGGC[A/G]GGGTGGCACGCGCCT | 197370 |
rs145165963 | snp | C/T | 4.99114e-05 | 0.00499532 | missense, utr-variant-5-prime | NSMCE1 | GRCh38.p7 | 16:27257467 | CAGTGCGTCTGCAAG[C/T]GCTTCACGTCCCATT | 197370 |
rs145237516 | snp | A/G | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27232030 | CCAGGAACTGAATTC[A/G]GGTCAGGTTCCTGGG | 197370 |
rs145275146 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27259217 | TCCACCTCCTTAGCC[C/T]CTTTCCTCTCCCAAG | 197370 |
rs145309141 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27253213 | AGTTATGGGAACCAC[C/T]GATGTACAGCCATTG | 197370 |
rs145395618 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27225537 | CTGGGTTCTAGAAAG[C/T]CCTCTGGAGCGGTGC | 197370 |
rs145410046 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27236572 | AAAGTGCTGGGATTA[C/T]AGGCGTGAGCCACCA | 197370 |
rs145425010 | in-del | -/A | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27260168 | AATGCTTCTATCTTT[-/A]AAAAAAAGTTTTTAA | 197370 |
rs145620887 | snp | A/C/G | 0.0558544 | 0.157504 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27236360 | GGAGTGCAGTAGCAC[A/C/G]GTCTTGGCTCACTGC | 197370 |
rs145681676 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27232591 | GACACACCCAGCCCC[A/G]AAGGGGAAACAACGA | 197370 |
rs145707034 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27260736 | TAGTGGCACACCTCC[A/G]TAGTCCCAGCTATTT | 197370 |
rs145749588 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27260126 | TTAAATCCAAGTTAA[C/G]TGTATAAAACAGTAA | 197370 |
rs145798727 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27243074 | GCAGGGAGCTGGCGG[C/T]ACGCATTCTACCAAA | 197370 |
rs145870327 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27226591 | GATGGCCTCCGCCAG[C/G]TCTTGTGGGAGGATG | 197370 |
rs146029413 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27231320 | GACCAGCCATGAAGA[A/G]GTCATAACCCCTACC | 197370 |
rs146032465 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27227378 | GAGTCTGGAGAGGGC[A/G]GACAGGCCCCATCAC | 197370 |
rs146112936 | snp | A/T | 0.00676609 | 0.0577691 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27252137 | TCTAAAACTCTTAGA[A/T]TTCCCTGAGTCATAT | 197370 |
rs146235012 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27231529 | GTGATTCCAGCTACT[C/T]GGGAGGCTGAGGCAG | 197370 |
rs146330072 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27227646 | TCCACAGTCAGCTCA[A/T]GCATCGGATATGAAC | 197370 |
rs146394420 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27245799 | AACTGAAAGGCAGAC[C/T]GGCTCTGACAGTGGT | 197370 |
rs146592195 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, intron-variant, synonymous-codon | NSMCE1, FLJ21408 | GRCh38.p7 | 16:27268713 | TTACCCACCAGGGAG[C/T]CCAAGCGCATCCCAG | 197370 |
rs146652761 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27237891 | CACTTCCTCCTACTG[C/T]ACTCGCTCACTGCAC | 197370 |
rs146708891 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27243364 | ATTTCTCACACAGGC[C/T]GGACTGTGAGCAGCT | 197370 |
rs146908812 | snp | A/T | 0.000399281 | 0.0141238 | missense | NSMCE1 | GRCh38.p7 | 16:27225815 | ACGCAGGGTAAGTGC[A/T]TCCTGATCCCACAGG | 197370 |
rs146954701 | snp | A/G | 0.00279162 | 0.0372561 | upstream-variant-2KB, intron-variant | NSMCE1, FLJ21408 | GRCh38.p7 | 16:27270188 | AAGCAATACAGCATA[A/G]CAATTACTTATATAG | 197370 |
rs146993138 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27247709 | AGGTGGGCAGATCAC[A/G]AGGTGAGGGGATCAA | 197370 |
rs147097857 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27230224 | CAGCACCTCCATGCC[A/G]GGCCAGTCTCACACA | 197370 |
rs147381061 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27263817 | TTATCTACTAAGTGA[C/T]GTCTACAAAAAACCT | 197370 |
rs147449131 | snp | A/G | 0.00174119 | 0.0294544 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27235168 | CTAGAGGGCTCTGCC[A/G]GGCACTCACCAACGC | 197370 |
rs147504286 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27230990 | ATAAAGCTGGGGGCA[C/T]GCCCTGCAAGCCATG | 197370 |
rs147863163 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27247615 | AGTCAGGTACGCATT[A/G]TCTAGAATTTCACAT | 197370 |
rs147953353 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27232352 | AGCAGGACTAGACGT[C/G]GGGGTGGGGGCAACA | 197370 |
rs147975591 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27229001 | CAACGCACTCGCTAC[C/T]GAACAAGCCTGGCCC | 197370 |
rs148021449 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27234397 | CAGGCACTGCGGGCC[A/G]CAGGGATGGATCTGT | 197370 |
rs148231504 | snp | C/T | 3.506e-05 | 0.00418674 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27226670 | ACCTGTACAGAGCCC[C/T]GGGAGCCGAGGGCCC | 197370 |
rs148304840 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27245461 | AGCGTGAAGCGCACA[A/G]AAATCCTGGCTCAGC | 197370 |
rs148542993 | snp | C/T | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27227846 | GGTGGAATGCAATGG[C/T]ACAATCTTGGCTCAA | 197370 |
rs148647702 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27258653 | GCTACCTTAAAGACA[A/T]AGAGGAAGCCTAAAT | 197370 |
rs148697865 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27265021 | CAGAAAAAAGATGCT[C/G]AATCTCAATGTTATC | 197370 |
rs148716863 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27232199 | AGGAAGCGGGGACCC[A/G]GCGTGAGTGCGTCCT | 197370 |
rs148770071 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27237002 | AATGGAGGATGTGGC[C/T]GTGTGAAAGAGTCAA | 197370 |
rs148773964 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27252609 | GCCACAGAAGAAGAC[C/T]CCCGTCTCTACAAAT | 197370 |
rs148842403 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27230723 | GGGCTACTGCCCAGC[A/G]CCAGTGCTGAGGGCC | 197370 |
rs149000104 | snp | A/G | 0.00835141 | 0.0640778 | upstream-variant-2KB, intron-variant | NSMCE1, FLJ21408 | GRCh38.p7 | 16:27269359 | CGAGAGGCAGAGGTT[A/G]CAGTGAGCCAGATCG | 197370 |
rs149036292 | snp | A/C | 0.0178098 | 0.0926698 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27247400 | TTCCTGAGGCCTCCC[A/C]AGCCATGCTGAACGG | 197370 |
rs149088327 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27253621 | CGAGGCCTCCTGTGC[C/T]GACTTCTATCAAGGA | 197370 |
rs149210988 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27225554 | CTCTGGAGCGGTGCA[C/T]GTAGCTCAGCCTTTA | 197370 |
rs149362907 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27249859 | ATTTGGGGAGAATTG[A/T]TACCTTAACAATACT | 197370 |
rs149417427 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27257787 | TGGATTCTGGAGCTA[A/G]AATGCCGGGATTCAG | 197370 |
rs149505515 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27238259 | GCCACACACAGTCTC[A/G]CCTCCAGCCTCACAC | 197370 |
rs149526897 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27227189 | AGGGGGTCAGTCTCC[C/T]CAGGGTGCAAACCCA | 197370 |
rs149558885 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27245034 | TCTGATAGTCACCCC[C/T]CACCACTCACCCCCA | 197370 |
rs149562251 | in-del | -/A | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27232943 | AGTACGATTTTGGAG[-/A]AAAAACTGTTATTCA | 197370 |
rs149727810 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27259924 | AGAGAATTCTATAAC[A/G]AGCTGAAGACTGAGG | 197370 |
rs149781615 | snp | A/G | 0.00398564 | 0.0444627 | upstream-variant-2KB, intron-variant | NSMCE1, FLJ21408 | GRCh38.p7 | 16:27268932 | CTCTCGATCCTTAAT[A/G]ATGGGAAGGGGCTTC | 197370 |
rs149909880 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27247271 | TGAGTGAGTTCTCAA[C/G]AGATCTGACAGTTTT | 197370 |
rs149999204 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27231533 | TTCCAGCTACTTGGG[A/C]GGCTGAGGCAGGAGA | 197370 |
rs150078292 | in-del | -/GA | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27233434 | GGCCTCGGAGGCAGT[-/GA]GAGAGAGACACGGCA | 197370 |
rs150170308 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27243851 | CCCTGAGGTCTCGCA[A/G]TGTTGCCCAGGCTGG | 197370 |
rs150223351 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27248920 | TCCAACCTCTGCCTC[C/T]CAGGCTCAAGCAACC | 197370 |
rs150311597 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27232867 | GGGGTCACTGCTGGA[A/G]TGCATGAAAGCAGAT | 197370 |
rs150375125 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27237986 | CCTGCATCAGGGTCA[C/T]GTCCACGATCTCCAT | 197370 |
rs150464172 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27262769 | AAACTTAAGAGCTTC[C/T]GCACAGCAAAAGAAA | 197370 |
rs150501804 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | FLJ21408, NSMCE1 | GRCh38.p7 | 16:27270805 | AAAGGCAGACCCGTT[C/G]CTAGGCAAGGAGGGG | 197370 |
rs150638111 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27234736 | CAGCCAGATGTCCTC[C/T]GACCAGCTGAGGTGT | 197370 |
rs150690811 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27240317 | TAGGACACCAGAGGT[A/G]GTACCCAAAGAGGAG | 197370 |
rs150725455 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27226974 | ACCAACCCCAGCCAA[C/T]GGGCATCAGCCACAT | 197370 |
rs150762157 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant, upstream-variant-2KB | NSMCE1, FLJ21408 | GRCh38.p7 | 16:27266573 | AGTGAGCCAAGATCG[C/T]GTCACTGCACTCTAG | 197370 |
rs150827813 | in-del | -/AG | | | downstream-variant-500B | NSMCE1 | GRCh38.p7 | 16:27224988 | GCTCGAGAACACAGA[-/AG]CGGGCTGCAGCAACT | 197370 |
rs150953655 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27237273 | AGGCATCAGGAGGGA[A/G]GCATGGCCTGACTTC | 197370 |
rs151003733 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27243637 | AGGATCAGTAACTGA[C/T]ACTACCCTAATTGAT | 197370 |
rs151079979 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27232753 | CAAGTCCCTGGGCGC[A/G]GCTCCTGGCTCTGCC | 197370 |
rs151284611 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27254285 | GGACAAAATAGATTG[C/T]TCTACCCTGTTCACC | 197370 |
rs180767002 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27231519 | GCGCATGCTTGTGAT[G/T]CCAGCTACTTGGGAG | 197370 |
rs180832935 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27265998 | CTTAACTTGGTGGCA[A/G]GTACATGAGTGTTCA | 197370 |
rs180836166 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27252428 | TCTAATGGTGGATTC[A/G]CAATTTTGTGGGATT | 197370 |
rs180888729 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27245054 | ACTCACCCCCAGCAA[C/T]TGGGATTAGATGGCA | 197370 |
rs181082311 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27239402 | GGCTAAAGGCATGTC[C/T]GAGGATCCTTTTGAC | 197370 |
rs181091840 | snp | C/G | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | NSMCE1, FLJ21408 | GRCh38.p7 | 16:27270273 | GGAGGATTTGTGTAG[C/G]TTAAATGCAAGTATT | 197370 |
rs181095944 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27259288 | CACACAATCATACCA[C/T]ACACCTGAGCATCGA | 197370 |
rs181117005 | snp | A/G | 0.00146097 | 0.0269879 | missense | NSMCE1 | GRCh38.p7 | 16:27225174 | AATGCTGCCTGGACC[A/G]CAGGGACTTTTTGTT | 197370 |
rs181132344 | snp | C/T | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27248069 | TATTGCTAAGTAGTA[C/T]GGATTTATCACAGTC | 197370 |
rs181326041 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27243644 | GTAACTGATACTACC[C/T]TAATTGATTTTATTT | 197370 |
rs181333647 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27265370 | GATGGGGTCTCACCT[A/G]TTGCCCCAGCTGGTC | 197370 |
rs181521773 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | NSMCE1 | GRCh38.p7 | 16:27224665 | AGGGAGGGAGAGCAC[A/G]CATCCCGCCCAAACG | 197370 |
rs181532761 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27247751 | CTAACACAGTGAAAC[A/C]CCATCTCTACCAGAA | 197370 |
rs181714948 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27257381 | GTACCTATGTCACTG[A/G]TCCCTGATCAACACA | 197370 |
rs181725816 | snp | C/T | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27252764 | TCTCTACTAAAACCA[C/T]AAAAATTAGCCGGGT | 197370 |
rs181763331 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27232781 | GCCATTCTGGCTGTG[A/G]CATCCTGAACACATC | 197370 |
rs181849150 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27237747 | CTATTGGACTTTCCA[C/G]ACACCCCGTTGCAGG | 197370 |
rs181916029 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27257031 | AGCTGCCCTGTGTCC[A/C]TCAATACCCCACTAG | 197370 |
rs181922277 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27225674 | TCCCTGGCACCAGGC[C/T]CCACGTCCTGCTGGC | 197370 |
rs181942888 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27243394 | TCAAAGGAATGGACC[A/G]TGTTACACTCATTCT | 197370 |
rs181958131 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27237050 | GAGCTCTGTCAGAGG[A/C]TCAGACTGTGGGGCC | 197370 |
rs182229190 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27264507 | ACGGAAAGGTATACA[C/T]ATATGGATACTTGAT | 197370 |
rs182248029 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | NSMCE1, FLJ21408 | GRCh38.p7 | 16:27270387 | AGAAAGTTTAATTCA[C/T]ACAGAGCTGGCTGAA | 197370 |
rs182260339 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27234876 | GGGTGAACGGGGAGT[C/T]GGCGGCAGGAGGGAT | 197370 |
rs182265126 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27254216 | GTTTAAAATCTCCCT[A/G]ATAACAAGAACATGC | 197370 |
rs182458649 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27248528 | CAATTCTCCTGCCTC[A/G]GCCTCCCAAGTAGCT | 197370 |
rs182623126 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27246675 | TTTTATTTTATGTAG[A/C]TACAGTGTTTCGCCA | 197370 |
rs182630037 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | NSMCE1, FLJ21408 | GRCh38.p7 | 16:27267548 | GTGAGTGAACAGAAC[A/C]ACTACAATCCAGGTC | 197370 |
rs182847444 | snp | A/C | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27249274 | GTATTTTTTAATGTA[A/C]ATTTTTAATTGTGAA | 197370 |
rs182850158 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27250126 | ATCCTACAACTTTAC[C/T]AAACTCACTTATTAG | 197370 |
rs182883576 | snp | A/G | 0.000136761 | 0.00826813 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27226700 | CAGTGATGAGCTCCC[A/G]TGCCCTGCCCTGCGG | 197370 |
rs183085361 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27227419 | GTGGAGCCTCCAGTG[C/G]AAGCCAGGCCTCCTG | 197370 |
rs183128649 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27233392 | TTAATGTCCCCAAAT[A/C]AAAGAGGGTCGCCTT | 197370 |
rs183281228 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27235050 | TATTCCTAATATTCT[A/G]TACATTTGGAGTGAC | 197370 |
rs183287327 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27255427 | GGTTCTTCATGATCT[C/G]CAAACCTACACACGA | 197370 |
rs183403053 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27253461 | GCCCATCTCTCGAAA[G/T]ATCACTGGCCTTGAC | 197370 |
rs183458785 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27260226 | AAAAAACTAAATACA[C/G]AAAAATAATAACATA | 197370 |
rs183496290 | snp | G/T | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27229504 | AGATGAAGTAGACCT[G/T]GCACTGATCCCAAAG | 197370 |
rs183503981 | snp | A/G | 0.0513262 | 0.151752 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27251076 | GAACTCCCGACCTCA[A/G]GTGATCTGCCCACCT | 197370 |
rs183529473 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27259772 | CCACACAATACCAGA[G/T]ATTAAACACAATCAA | 197370 |
rs183626127 | snp | A/G | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27256721 | CATGTCCTGTCTCCA[A/G]GGGCTTCTTATTTGC | 197370 |
rs183633056 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-5-prime | NSMCE1 | GRCh38.p7 | 16:27241357 | AGCCAACTTACCCTC[C/T]GACAGCCCTCCCGAC | 197370 |
rs183655096 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27246096 | GCTGGAAACAAACCC[A/G]GGATGAAGGCAGATA | 197370 |
rs183655500 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27236785 | AATGAAACAGTCCCA[C/T]AGGAAAAGGCCCAGC | 197370 |
rs183853156 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27261428 | GACAAATATCTGCAA[C/T]TAACATACTTAAAAA | 197370 |
rs183889381 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27242092 | CCTGCGTTCATCATC[A/G]GAACTGAGTGATGGC | 197370 |
rs183934176 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NSMCE1, FLJ21408 | GRCh38.p7 | 16:27266841 | CAAGAACAAAAACTC[C/T]CTAAATTCAATGTTT | 197370 |
rs184042331 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27240366 | TGCATTGGATCAGCC[C/T]GGCCTGGCCCAGCCC | 197370 |
rs184334368 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | NSMCE1 | GRCh38.p7 | 16:27224681 | CATCCCGCCCAAACG[C/T]CCAGCCTCAGCCCAT | 197370 |
rs184337382 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27247788 | AAAAATTAGCCGGGC[A/G]TGGTGGCACACACCT | 197370 |
rs184345531 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | NSMCE1, FLJ21408 | GRCh38.p7 | 16:27270060 | AAGTACAGTCAGCTG[C/T]CCATGTTTACAGGTT | 197370 |
rs184386984 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | NSMCE1, FLJ21408 | GRCh38.p7 | 16:27268141 | TGAGGGTGAAACCTA[A/T]CATAGAACATAGGGA | 197370 |
rs184504475 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27247180 | AGTTCCCATAATCCA[A/C]ACATGTCATGGGAGG | 197370 |
rs184562260 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27230223 | TCAGCACCTCCATGC[C/T]GGGCCAGTCTCACAC | 197370 |
rs184620869 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27252135 | CTTCTAAAACTCTTA[A/G]AATTCCCTGAGTCAT | 197370 |
rs184644878 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27257107 | TCCCTGAACCATGCA[C/T]TTACTTATGTGTTAA | 197370 |
rs184747157 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27230650 | TGCCACATTAGCTTC[A/G]TTCCTTCGTCCTCCT | 197370 |
rs184894547 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27236389 | GCAACCTCCACCTCC[C/T]GGGTTCAAGCAGTTC | 197370 |
rs185059039 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27255862 | CTCGTGTCCCTTCAC[A/G]TTTTGAAAAGTATAA | 197370 |
rs185187910 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27264583 | GTTATCCATATGTAA[A/C]AAAATGAATAAAATT | 197370 |
rs185291703 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27243557 | GCAGGAAGCCAGGCC[A/G]GTCCCCTAGCAACCA | 197370 |
rs185397727 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27239451 | CATGGTCATGATAAA[C/G]AGTGCGGAATAAAGT | 197370 |
rs185407091 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27259515 | TCTTGAAGCAGGAAC[A/G]TGGTGTTGCCTAGCT | 197370 |
rs185421139 | snp | A/G/T | 0.0023933 | 0.0345097 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27247442 | AACTTCTTCCCTTTA[A/G/T]AAATTACCCAGTTTT | 197370 |
rs185556190 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NSMCE1, FLJ21408 | GRCh38.p7 | 16:27268477 | GCGTGTGTGTTGCGG[A/G]AGGACATCCCAGTCC | 197370 |
rs185637504 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27226920 | CTGTGATCCCACAGC[C/T]CAGTGCTCAGGAAGA | 197370 |
rs185644568 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27244780 | TGCCTCCGAGTTACG[G/T]TCTTTCTCTTTCTAA | 197370 |
rs185652018 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27265566 | TATACCTTACAGAAA[C/T]TTCCACATTTGCCCT | 197370 |
rs185696736 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27249499 | TTTGATTATGGATAT[A/C]CAATTATTCCAGCAC | 197370 |
rs185732996 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27242745 | GCTGTTCATACACAT[G/T]TCATCTAATCACACC | 197370 |
rs185873789 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27263361 | TGGAACACTATGCAG[C/T]CATAAAGAAGAATGA | 197370 |
rs185911780 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NSMCE1, FLJ21408 | GRCh38.p7 | 16:27266229 | ACAACAACAACAAAA[C/T]AATGTGAATATGTTA | 197370 |
rs185945023 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27252898 | CACTCCAGCCTGGGC[A/G]ACAAGAGCAAAACTG | 197370 |
rs185964161 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27225373 | CACTGCTAACCCTCC[C/T]CAGCCCGTGAGGAAG | 197370 |
rs186033762 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | NSMCE1, FLJ21408 | GRCh38.p7 | 16:27270369 | ACAGGGGAATTGCAA[C/T]AGAGAAAGTTTAATT | 197370 |
rs186105917 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27248128 | ACTAGGTGTTCACAT[C/T]TGGGGCCATTACAAA | 197370 |
rs186159222 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27249031 | GACGGAGTTTTGTCA[C/T]GTTGCCCAGGCTGGC | 197370 |
rs186201134 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27226523 | ACCAGGGAGGAGGGC[A/G]GCAGTGCGTCCCTGC | 197370 |
rs186264755 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27253941 | GGACTTTGTTTCCCC[G/T]TAACGACAGTAAGAA | 197370 |
rs186417784 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27252647 | AACTTAGCCGGGCGC[A/G]GTGGCTCATGCCTGT | 197370 |
rs186419641 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27233484 | AGACAGGTTCCTGCA[C/T]ACGCAGGTGTGTGCT | 197370 |
rs186452675 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27231748 | AATACAGCCTGGAGG[A/G]CAAGAACAACTGTGA | 197370 |
rs186506375 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27238517 | AGCAGCCATGTCCCT[C/T]CCTAACGAGACCTTC | 197370 |
rs186630973 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27234879 | TGAACGGGGAGTCGG[C/T]GGCAGGAGGGATGAG | 197370 |
rs186635997 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27254456 | CTTAGTACCAAGGCA[G/T]CATGTGGCTCCTTGC | 197370 |
rs186730070 | snp | C/T | 1.71416e-05 | 0.00292755 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27257431 | ACAGGGAAACGGTAC[C/T]CACGGTCATGGACCT | 197370 |
rs186766152 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27242159 | TGTTTGACTTTTTCC[A/G]TAATAAAATGTTGTA | 197370 |
rs186771146 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27262813 | AAACAGACAACCTAC[A/C]GAATGGGAGAAAATA | 197370 |
rs186778857 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27232852 | CCAAGTCCTCCCCAC[A/G]GGGTCACTGCTGGAA | 197370 |
rs186988724 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27246687 | TAGATACAGTGTTTC[A/G]CCATGTTGCCCAGGT | 197370 |
rs187007706 | snp | G/T | | | intron-variant, upstream-variant-2KB | NSMCE1, FLJ21408 | GRCh38.p7 | 16:27267592 | CCTCAAATCTAAAAA[G/T]GTATGAATACTAGTG | 197370 |
rs187291847 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27237089 | CTGAGAACAAAGCCC[A/C]GGGCAGTGACACTAA | 197370 |
rs187386100 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27245485 | GCTCAGCAACTCCAT[C/G]CTGGCCTGAAAGGGC | 197370 |
rs187462922 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27246257 | CTCACTGAAGTATTT[A/C]TAAACCTAAATTTTT | 197370 |
rs187638030 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27227434 | GAAGCCAGGCCTCCT[G/T]GTTCCCATGCCAGGG | 197370 |
rs187872974 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27229817 | CTCCTGACTTCAAGT[G/T]ATCTACCCGCCTTGG | 197370 |
rs187885532 | snp | A/T | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27251169 | TTTAAAATATATATA[A/T]ATATATATATATATA | 197370 |
rs187927053 | snp | G/T | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27250307 | TGAGAACAGACATTC[G/T]TGTCTTTCTCCTGAG | 197370 |
rs187975450 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27237007 | AGGATGTGGCCGTGT[G/T]AAAGAGTCAAGGAAA | 197370 |
rs188035337 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27256809 | CACACTCTTCAGGTC[C/T]GGCCCAGTCTAAGGC | 197370 |
rs188221156 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | NSMCE1 | GRCh38.p7 | 16:27241693 | AATGCTGGGAAGAGC[C/T]GGGTGGAAGGAGAGT | 197370 |
rs188431899 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | NSMCE1, FLJ21408 | GRCh38.p7 | 16:27267099 | GTTCATATATACAGA[A/T]AAACCAATTAAAAAA | 197370 |
rs188440112 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27236003 | TGAACTGACTCGCCC[A/G]GAGTTGCACCACAAG | 197370 |
rs188466971 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27260328 | TGAATAAATTTTACA[C/T]TTGCATTTTACAATT | 197370 |
rs188646583 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27248018 | ATCATTCTGATTCAT[C/T]CATATTCTAGCATGT | 197370 |
rs188699611 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27259926 | AGAATTCTATAACGA[A/G]CTGAAGACTGAGGAT | 197370 |
rs188702711 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | NSMCE1, FLJ21408 | GRCh38.p7 | 16:27270103 | ATTGAAGCAACTGTG[A/G]GTGGTTAATATTTGT | 197370 |
rs188729877 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27255631 | AGTGCTCTGGAGAAC[A/G]CAGATGCTACTCTCC | 197370 |
rs188958887 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27243616 | ATGGCCCAAAAGGAC[C/G]AAGGCAGGATCAGTA | 197370 |
rs188966756 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27264987 | TACAAAAAGAGGATG[C/T]ATAAATGATGAATAA | 197370 |
rs188968059 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27240778 | CTCCTTTTCTTTTAA[A/T]ATTAAATTTTAAGGC | 197370 |
rs189071193 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27248393 | AGTGGTAGCTCACTG[C/T]GGTTTTAGTTTGCTT | 197370 |
rs189195134 | snp | A/G | | | downstream-variant-500B | NSMCE1 | GRCh38.p7 | 16:27224562 | ATGCAGGAGGGTCAG[A/G]GAGAGGAAGCACTGA | 197370 |
rs189205954 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27247473 | GGGTATGTCTTTATT[A/C]GCAGCGCGAGAACGG | 197370 |
rs189213921 | snp | A/C | 0.000798403 | 0.0199641 | utr-variant-5-prime, intron-variant, upstream-variant-2KB, missense | NSMCE1, FLJ21408 | GRCh38.p7 | 16:27268735 | GCATCCCAGGCCGCG[A/C]TAGCGGATACGGTCG | 197370 |
rs189295320 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27232702 | CGGAACTGCCCTGCC[A/T]TGCAGTCTGTGGGCT | 197370 |
rs189309465 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27231412 | GAGGCTGAGGCAGGC[A/G]GATCACCTGAGGTCA | 197370 |
rs189312035 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | NSMCE1, FLJ21408 | GRCh38.p7 | 16:27270382 | AATAGAGAAAGTTTA[A/G]TTCACACAGAGCTGG | 197370 |
rs189522992 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27256116 | CTTGCTCCCTGTGTA[C/T]CTGTACACGCCCTTT | 197370 |
rs189531829 | snp | C/G | 0.00636936 | 0.0560724 | downstream-variant-500B | NSMCE1 | GRCh38.p7 | 16:27224709 | CATTCAGGCCAGTGG[C/G]ACCTTGGGCCAGGGG | 197370 |
rs189604186 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27252391 | GCCAGGCACGGTGGC[C/T]AAATAAATATTTCAA | 197370 |
rs189711341 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27239526 | ACCACTTTGAAGACT[C/T]AGGAGTTAATTAACA | 197370 |
rs189721912 | snp | C/T | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27259551 | TTAGGGAGATTATCC[C/T]CTTTGGCATCATGGA | 197370 |
rs189810704 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27252006 | GTTTCCCCTGTGCCA[C/T]GGCCTAGAAACTTTC | 197370 |
rs189837451 | snp | C/G | 0.00795532 | 0.062565 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27236517 | GGCCAGGCTGGTCTC[C/G]ATCTCCTGACCTCAA | 197370 |
rs189960810 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27244834 | CTGGGATCTGCTCAT[C/T]CTATTCACCACAGCA | 197370 |
rs189970439 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27265887 | ACTACAAAGCAAAAC[A/G]AGGCAACAAGTAACA | 197370 |
rs190025201 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27234460 | GCTCAGCCAACATGC[C/T]GGGCCCTCAGAAGTT | 197370 |
rs190054000 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27230283 | TTGGGGTGATATACC[C/G]ACCTGGAAGGGCCTT | 197370 |
rs190088027 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27237616 | GTCCACCCAGTGTGA[A/C]ACTGGGGCAAGTCCC | 197370 |
rs190278032 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27239212 | GAACTGGGGTCTCTT[A/G]CTTGCTCCCAAGATC | 197370 |
rs190349173 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27257202 | GTGTGAACCACAACT[A/G]TACAGCTTTAGACTC | 197370 |
rs190349732 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27264297 | AGGACTGCTTCAGCT[C/T]GGGATGTCGAGGCTA | 197370 |
rs190374291 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27246620 | CTCAGCCTCTGAGTA[C/T]CTGTGATTACAGGCT | 197370 |
rs190432554 | snp | C/T | | | intron-variant, upstream-variant-2KB | NSMCE1, FLJ21408 | GRCh38.p7 | 16:27267300 | TAAATCTCAGTCATA[C/T]CATTCGTGCGGGTGC | 197370 |
rs190590188 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27242748 | GTTCATACACATTTC[A/G]TCTAATCACACCCAC | 197370 |
rs190613658 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27226557 | GCACAGCAGGGAGGC[A/G]TCCTGACACGTCCTG | 197370 |
rs190671648 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27249259 | TTCAGTCTCTAAAGA[A/G]TATTTTTTAATGTAA | 197370 |
rs190926972 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27225434 | AACTGAGGGAGCTGT[A/G]GACATAGCTTTCACG | 197370 |
rs191181316 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27242690 | ATCATAATGGAAATC[A/G]TCATGAGAAACATAA | 197370 |
rs191191320 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27263080 | CAGAGAAAAGGGAAA[C/T]TTATATACTGTTGGA | 197370 |
rs191215131 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27254154 | AAATTAATAATATTG[A/G]GTCTTGCGAGTATTC | 197370 |
rs191226477 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27258895 | AGCTGGAACTACAGG[C/T]GCCCACCACCGTGCC | 197370 |
rs191232814 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27226991 | GGCATCAGCCACATC[C/T]CCCTGGCAGAGCCTC | 197370 |
rs191429541 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27249863 | GGGGAGAATTGATAC[C/T]TTAACAATACTGAAT | 197370 |
rs191439755 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27252957 | AAAGAAACCCTTGAA[C/T]GACAGGATTTGAAGA | 197370 |
rs191442202 | snp | G/T | 0.00795532 | 0.062565 | intron-variant, upstream-variant-2KB | NSMCE1, FLJ21408 | GRCh38.p7 | 16:27268109 | ATTTGATTACAAGCC[G/T]CTGCTCCAGCCCCCT | 197370 |
rs191450293 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27236540 | GACCTCAAGTGTTCC[A/G]CCCACCTCAGCTTCC | 197370 |
rs191507258 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27256160 | GCTTGGCTCACTTCT[A/G]TGTCATTTTTTATCT | 197370 |
rs191686252 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27232900 | GGGATCCGAGAAGGC[C/T]GGGCTCCTCAGACAT | 197370 |
rs191705647 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27242074 | AAATAAAACAAGATC[A/G]GTCCTGCGTTCATCA | 197370 |
rs191763348 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27260906 | TCGTGGTGGCTCACA[C/T]CTATAATCCTAGCAC | 197370 |
rs191779872 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27241314 | AATAACAGCAAAAAA[C/T]AAGACTCCAAGGGCC | 197370 |
rs191968873 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NSMCE1, FLJ21408 | GRCh38.p7 | 16:27266281 | AAATGAGAATGAGAA[A/C]AGGATAGGATTGAAT | 197370 |
rs192033900 | snp | A/C/G | 0.00199481 | 0.0315187 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27260084 | GCAGGGTAGAATAAA[A/C/G]AGCAAAAAAAGTTGG | 197370 |
rs192080167 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | NSMCE1, FLJ21408 | GRCh38.p7 | 16:27269690 | TGTGAGAAAGCAAGT[A/G]AAATTACTCGTGGAA | 197370 |
rs192252384 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27250560 | ACTTTGGGAAGCCAA[A/G]CCAGGGAGATCACTT | 197370 |
rs192312907 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27230038 | TCTCCCAGGCGCCTC[A/G]CCACAACACTTGGAA | 197370 |
rs192319641 | snp | A/T | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27251177 | ATATATATATATATA[A/T]ATATATATATATAAA | 197370 |
rs192341879 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27245662 | CTGTCTAAGCACTTA[A/G]TAACTGCCGGCTGTC | 197370 |
rs192476043 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27247166 | TCATCTTGAATTGTA[A/G]TTCCCATAATCCAAA | 197370 |
rs192528514 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27234894 | CGGCAGGAGGGATGA[A/G]GCCCAAATCCCTACC | 197370 |
rs192531801 | snp | A/G | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27255289 | TGGTACAACTGCGGC[A/G]CATCTACCTTCACCA | 197370 |
rs192655722 | snp | C/T | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27229349 | CTGCAGTGAGATGAC[C/T]GTCTCACTGATCTCG | 197370 |
rs192747301 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27230621 | AACCTGGAGGAGTCT[C/T]ACCACACAGCCCCTG | 197370 |
rs192878592 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27255747 | TTCTGTTCTGTCTCC[C/G]TCTTCTTATTCCCAT | 197370 |
rs192960231 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27252046 | TGAGCTGGGGCAGCT[A/G]TACTGCTCACTCCCA | 197370 |
rs193078716 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27236192 | CAGGAGCCCGTGGCC[A/G]GGGACAGCAGGGCCT | 197370 |
rs193122932 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | NSMCE1, FLJ21408 | GRCh38.p7 | 16:27268290 | AGCACGGAGGGCGGC[A/G]GGACAAAGAGGGTGG | 197370 |
rs193273931 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27247339 | TCCTGCCTGCCACCA[C/T]GTGAAGAAGGATGTG | 197370 |
rs199533829 | snp | A/C/G | 0.000112946 | 0.00751402 | missense | NSMCE1 | GRCh38.p7 | 16:27225203 | TTCGATTTCAAGACA[A/C/G]CAGACTCCCTCTCCT | 197370 |
rs199598545 | snp | C/T | 1.65894e-05 | 0.00288 | missense | NSMCE1 | GRCh38.p7 | 16:27226758 | TATTGCAGATCTTCA[C/T]CGCGTCGGGGTACGT | 197370 |
rs199640995 | snp | A/G | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27255101 | ACCAGGCTGGTCTTG[A/G]ACTCCTGACCTCAGG | 197370 |
rs199657281 | snp | C/T | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27265024 | AAAAAAGATGCTCAA[C/T]CTCAATGTTATCAGA | 197370 |
rs199659956 | in-del | -/TTA | 0.0178168 | 0.0926875 | intron-variant, upstream-variant-2KB | NSMCE1, FLJ21408 | GRCh38.p7 | 16:27267201 | TCTATACGTTTAAAT[-/TTA]TTATTAAATTAATTA | 197370 |
rs199668282 | snp | C/T | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27238542 | ACCTTCGCCTTTTTT[C/T]TTTTTTTTTTTTTAC | 197370 |
rs199674012 | snp | A/C | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27231731 | AACATTCCCTAGTGC[A/C]AAATACAGCCTGGAG | 197370 |
rs199725386 | snp | A/G | 0.00024899 | 0.0111549 | synonymous-codon | NSMCE1 | GRCh38.p7 | 16:27225835 | GATCCCACAGGTTTC[A/G]CAGCTTTGACCCTGA | 197370 |
rs199864121 | in-del | -/T | | | intron-variant, upstream-variant-2KB | NSMCE1, FLJ21408 | GRCh38.p7 | 16:27267735 | TGCATTTTTTTTTTT[-/T]GAGACGGAGTTTCGC | 197370 |
rs199965487 | snp | A/G | 3.3123e-05 | 0.00406945 | synonymous-codon | NSMCE1 | GRCh38.p7 | 16:27233096 | GATCAACCAGGTTCA[A/G]TATGTTTGTGGAAGA | 197370 |
rs199976503 | in-del | -/TATATAAATATATATATATATAT | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27251185 | ATATATATATATATA[-/TATATAAATATATATATATATAT]AAAACTCTGTAGAGT | 197370 |
rs200032590 | snp | C/T | 0.000248457 | 0.011143 | synonymous-codon | NSMCE1 | GRCh38.p7 | 16:27233112 | TATGTTTGTGGAAGA[C/T]GCAAAGCCGGTTTCT | 197370 |
rs200141326 | snp | A/G | 0.000170602 | 0.00923427 | missense, utr-variant-5-prime | NSMCE1 | GRCh38.p7 | 16:27257435 | GGAAACGGTACTCAC[A/G]GTCATGGACCTTGTA | 197370 |
rs200309912 | snp | A/G | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27236645 | ATTATTGTTTTCACT[A/G]CTGTTTTTATGTATT | 197370 |
rs200340307 | snp | A/C | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27244656 | ACATATGGCAGCTCC[A/C]CAGAAAGGTTTGAAC | 197370 |
rs200406906 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27249848 | TCTATAGATCAATTT[A/C]GGGAGAATTGATACC | 197370 |
rs200523800 | in-del | -/T | 0.480382 | 0.097079 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27250844 | ATTTAATTTTAACTG[-/T]TTTTTTTTTTTTTTT | 197370 |
rs200623855 | snp | A/G | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27255071 | TTTTAGTAGAGATGG[A/G]GTTTCACCATGTTGA | 197370 |
rs200675037 | snp | A/G | 0.00199791 | 0.031543 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27225886 | GCGGAGCTGGTGCAC[A/G]CCTCCATGTTCTGCA | 197370 |
rs200738747 | in-del | -/TCA | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27236640 | TATGTATTATTGTTT[-/TCA]CTACTGTTTTTATGT | 197370 |
rs200850334 | in-del | -/C | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27227787 | CTTTTCTTTTCTTTT[-/C]TTTTTTTTTTTTTTT | 197370 |
rs200941291 | in-del | -/C | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27236646 | TTATTGTTTTCACTA[-/C]TGTTTTTATGTATTA | 197370 |
rs200970237 | snp | A/G | 0.000116108 | 0.00761845 | missense | NSMCE1 | GRCh38.p7 | 16:27226760 | TTGCAGATCTTCACC[A/G]CGTCGGGGTACGTCT | 197370 |
rs200999779 | snp | C/T | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27227783 | CGTTTCTTTTCTTTT[C/T]TTTTTTTTTTTTTTT | 197370 |
rs201079706 | in-del | -/TTTCT | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27227770 | GAGCTGTCACTCCCG[-/TTTCT]TTTCTTTTCTTTTTT | 197370 |
rs201091849 | snp | A/G | 0.000132807 | 0.00814774 | synonymous-codon, utr-variant-5-prime | NSMCE1 | GRCh38.p7 | 16:27235289 | CTCCAACTTATCTAC[A/G]GTGGCATTGCCTGGA | 197370 |
rs201184523 | in-del | -/TA | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27264247 | CATGATGGTATGCAC[-/TA]CTGTAGTCCCAGGTA | 197370 |
rs201195924 | in-del | -/C | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27239961 | CTTATTATGTGCCAG[-/C]CACTATGCATTCACA | 197370 |
rs201199834 | snp | A/G | 0.000285175 | 0.0119376 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27225722 | CTCCTCAGGGCCCAC[A/G]CACTTGGGATCTCGT | 197370 |
rs201300433 | in-del | -/T | 0.029116 | 0.117091 | intron-variant, upstream-variant-2KB | NSMCE1, FLJ21408 | GRCh38.p7 | 16:27266866 | ATGTTTAGAACTGAA[-/T]TTTTTTTAACTAAGC | 197370 |
rs201322789 | in-del | -/ATATATATATATATATATATAA | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27251170 | TTAAAATATATATAT[-/ATATATATATATATATATATAA]ATATATATATATATA | 197370 |
rs201449764 | snp | C/T | 0.00159155 | 0.0281646 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27225686 | GGCCCCACGTCCTGC[C/T]GGCCCAGCCCCTCCC | 197370 |
rs201460413 | snp | A/G | | | intron-variant, upstream-variant-2KB | NSMCE1, FLJ21408 | GRCh38.p7 | 16:27266622 | ACTCTGTCACAAAAA[A/G]AAAAAAAAAATTACT | 197370 |
rs201527627 | snp | A/G | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27255091 | CACCATGTTGACCAG[A/G]CTGGTCTTGAACTCC | 197370 |
rs201559274 | in-del | -/TATAAATATATATATATATAT | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27251187 | ATATATATATATATA[-/TATAAATATATATATATATAT]AAAACTCTGTAGAGT | 197370 |
rs201565333 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27237819 | CACCTCTGGTTTGGC[C/T]TCCAGCCTCATTTTT | 197370 |
rs201673345 | in-del | -/CAATGGAA | 0.0138799 | 0.0821421 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27262403 | AACAGGCACATACAC[-/CAATGGAA]CAATGGAACAGAATA | 197370 |
rs201683540 | snp | A/C | 9.98153e-05 | 0.00706383 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27235146 | TTCCAGCTCCTCAAA[A/C]ATGCCACTAGAGGGC | 197370 |
rs201847643 | snp | G/T | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27239931 | AAGGGGCCTGCAAAT[G/T]TGTGGCTATGATTAC | 197370 |
rs201911122 | in-del | -/CAC | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27236641 | ATGTATTATTGTTTT[-/CAC]TACTGTTTTTATGTA | 197370 |
rs201915035 | in-del | -/C | 0.0283406 | 0.115616 | intron-variant, upstream-variant-2KB | NSMCE1, FLJ21408 | GRCh38.p7 | 16:27267802 | GGCACGATCTTGATT[-/C]ACTGCAACCTCCGCC | 197370 |
rs201971697 | snp | A/G | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27248536 | CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGACTAC | 197370 |
rs202042105 | snp | C/G | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27226250 | GTGCCCAAGGATACA[C/G]GTGTACGAGGCCCGT | 197370 |
rs202238055 | snp | A/G | 1.65784e-05 | 0.00287905 | synonymous-codon, utr-variant-5-prime | NSMCE1 | GRCh38.p7 | 16:27235268 | GTTAATGTTGTTGAT[A/G]AAGTCCTCCAACTTA | 197370 |
rs367626085 | snp | A/G | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27237547 | GCAGCTCAGGTGCAA[A/G]AGGCCCAGACATCAA | 197370 |
rs367630563 | snp | C/T | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27247664 | GGGCACAGTGGCTCA[C/T]ACCTGTAATCCCAGC | 197370 |
rs367692889 | snp | C/T | 3.31312e-05 | 0.00406995 | missense | NSMCE1 | GRCh38.p7 | 16:27233017 | TCAATCAGCCACTTG[C/T]TTTGAACAAACTTCT | 197370 |
rs367715497 | snp | A/G | 0.000116443 | 0.0076294 | synonymous-codon | NSMCE1 | GRCh38.p7 | 16:27225760 | GTAGTCGTTGCAGTG[A/G]GGGCAGCGCGGTTCA | 197370 |
rs367839206 | snp | A/G | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27232721 | AGTCTGTGGGCTAGA[A/G]CCTTGATCCTGGGGC | 197370 |
rs367860950 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27243116 | TGCTCTGCTCCAGCC[A/G]AGTGCCCGAGTTTTG | 197370 |
rs367982402 | snp | C/T | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27254521 | CTTACAGTCAAGACT[C/T]ACAGGAGAAAAAAAG | 197370 |
rs367986038 | snp | A/T | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27261650 | TAGTCTAAAAACAAA[A/T]AATTTCAAATGTTAC | 197370 |
rs368079529 | snp | C/T | 0.000159987 | 0.00894249 | missense | NSMCE1 | GRCh38.p7 | 16:27225801 | GGAAGTACTTGGCCA[C/T]GCAGGGTAAGTGCAT | 197370 |
rs368113220 | snp | A/G | | | intron-variant, upstream-variant-2KB | NSMCE1, FLJ21408 | GRCh38.p7 | 16:27267405 | CTGACCCCATCTTAC[A/G]GATGAGGAAACTGAG | 197370 |
rs368184271 | snp | A/G | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27229088 | CCAAGCCCCTAATAC[A/G]CGTATCTCCCGGGCT | 197370 |
rs368227333 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27257038 | CTGTGTCCATCAATA[C/T]CCCACTAGGCACTGT | 197370 |
rs368271449 | snp | C/T | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27242582 | CCTATCTATGCAGCA[C/T]CTATGGGACCTTCCC | 197370 |
rs368320768 | snp | C/T | 8.31207e-05 | 0.0064462 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27235154 | CCTCAAAAATGCCAC[C/T]AGAGGGCTCTGCCGG | 197370 |
rs368368377 | in-del | -/A | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27236963 | AGTTAAAAAAAAAAA[-/A]CAACAGAAGATCATG | 197370 |
rs368368776 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27250224 | CAGTTTTACTGTGTC[A/G]TCCTTTCTAATCCAG | 197370 |
rs368375612 | snp | C/T | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27228746 | GATCCATCATGGTAC[C/T]CCACCTCTCCAGCCC | 197370 |
rs368410925 | snp | A/C/T | 3.35824e-05 | 0.00409757 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27225721 | GCTCCTCAGGGCCCA[A/C/T]GCACTTGGGATCTCG | 197370 |
rs368454081 | snp | A/G | 0.000169443 | 0.00920286 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27226851 | TCTGCAGGGACACAC[A/G]GGAGGTGGCCACCCT | 197370 |
rs368492337 | snp | A/G | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27236852 | AGGAAGGGACTAAAC[A/G]AAGGGTCATCACAGG | 197370 |
rs368617071 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27259365 | CTTTATTTCCTATCA[C/T]TAGGGCCATTCCATG | 197370 |
rs368667166 | snp | A/G | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27242662 | CCACTGCTTTATCAC[A/G]GTAAAGTTCTGGATC | 197370 |
rs368668986 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27257284 | AAGTGGAAGATGAAA[C/T]TAGAAAGATGGGCCC | 197370 |
rs368673655 | snp | A/G | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27232751 | CCCAAGTCCCTGGGC[A/G]CGGCTCCTGGCTCTG | 197370 |
rs368696470 | snp | C/G | | | intron-variant, upstream-variant-2KB | NSMCE1, FLJ21408 | GRCh38.p7 | 16:27266328 | AAAGGAGTGGGAAAA[C/G]TAGGAGTGGAAGAAA | 197370 |
rs368699286 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27239767 | AGAGATACCCTAGCC[A/C]GGACAACCAGCAACA | 197370 |
rs368861984 | snp | C/T | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27233830 | AGTGGGGACTGGGAC[C/T]GGGCCTTTCTAACAA | 197370 |
rs368910898 | snp | A/C | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27229439 | CCTGTGTCCGCAGCA[A/C]CTGCTGTGGGGCCCA | 197370 |
rs368917202 | snp | C/T | 1.68108e-05 | 0.00289916 | missense, utr-variant-5-prime | NSMCE1 | GRCh38.p7 | 16:27257566 | CTCCTTGTGCTGCCC[C/T]GCATGTGGGAACGAA | 197370 |
rs369013355 | snp | A/G | 3.32171e-05 | 0.00407522 | synonymous-codon | NSMCE1 | GRCh38.p7 | 16:27226735 | CTGGATGAGGAGGCT[A/G]TGACAGATATTGCAG | 197370 |
rs369034649 | snp | C/T | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27250982 | GAGCAGCTGGGATTA[C/T]AGGCATGCACCACCG | 197370 |
rs369232365 | snp | C/T | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27230132 | AGCTCCCATGAGCCG[C/T]GCTTGCTCTCAGAGG | 197370 |
rs369247574 | snp | C/T | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27238623 | ATGATATTCAGGGAA[C/T]CAGAAAGCAGAAAGC | 197370 |
rs369289311 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27252240 | AATGACCAAGCCTCA[A/G]TAAAAAACATGGAAC | 197370 |
rs369305004 | in-del | -/TA | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27242058 | AAGCAGGTACAAACA[-/TA]AATAAAACAAGATCA | 197370 |
rs369305613 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27236719 | TGGAAAAAAAACTGC[A/G]AGAAAAAATGGACAA | 197370 |
rs369307486 | snp | C/T | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27230813 | CCTCGAGCTCAGAGG[C/T]GCCCTGCAGAAGGTG | 197370 |
rs369425214 | snp | C/T | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27257919 | TCTGCAGAACTGCTA[C/T]GAAGATTAGATGGGT | 197370 |
rs369426936 | snp | A/C | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27235022 | TTCTAAATAAAAAAC[A/C]ATTTTCTCCCTTTAT | 197370 |
rs369428811 | snp | C/T | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27227047 | CTAAAGACATGGAGG[C/T]GTGGCTCCCTGACAC | 197370 |
rs369513785 | snp | A/G | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27225933 | ACAAGGGAAATGGGC[A/G]GCAGGTGGCATCGTG | 197370 |
rs369567534 | snp | G/T | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27232979 | AAAAGTGAACCAGGC[G/T]GGAAAAACCATGAGA | 197370 |
rs369629311 | snp | A/G | 0.000163861 | 0.00905005 | utr-variant-3-prime | NSMCE1 | GRCh38.p7 | 16:27225152 | CCCTCAGCAGGGCAC[A/G]ATGGCTAATGCTGCC | 197370 |
rs369701840 | snp | C/T | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27251350 | AGATTTTGTCAAATA[C/T]TTTTTCTGTACCTAT | 197370 |
rs369883479 | snp | G/T | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27259685 | AATGATACGAATCAC[G/T]GTCATTGTGATCCCA | 197370 |
rs369926485 | snp | A/G | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27226237 | AAATAATCACCAGGT[A/G]CCCAAGGATACAGGT | 197370 |
rs369926670 | snp | C/G | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27226438 | TACCAAGATGATGCA[C/G]GTTGCACAGAACACT | 197370 |
rs370015684 | snp | A/G | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27265261 | CAGCCTTGACCTTGT[A/G]GGCTCAATCGATCCT | 197370 |
rs370020355 | snp | C/T | 0.000696252 | 0.0186451 | synonymous-codon | NSMCE1 | GRCh38.p7 | 16:27225172 | CTAATGCTGCCTGGA[C/T]CGCAGGGACTTTTTG | 197370 |
rs370027258 | snp | A/G | 6.23189e-05 | 0.00558172 | synonymous-codon | NSMCE1 | GRCh38.p7 | 16:27225229 | CTCCTTCTCAGGGTC[A/G]AAGACTTCTGTAGAC | 197370 |
rs370256150 | snp | C/G | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27254912 | TGATACATGGTCTCG[C/G]TCTGTCGCCCAAGCT | 197370 |
rs370317898 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27265927 | GGGCGGTGGTTATCT[C/T]TGAGGAGGGAAGAAA | 197370 |
rs370384825 | snp | C/T | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27240498 | CATCCATCATCCCCT[C/T]GGCCCAGCCCTGAGC | 197370 |
rs370437701 | snp | A/G | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27261764 | GATGTCAAAAGAAAG[A/G]AAAATTACAAGCCAG | 197370 |
rs370509797 | snp | C/T | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27234429 | ACCAGGCGTATATTA[C/T]AGACTTTATTCTTTA | 197370 |
rs370555949 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27261092 | GAATCGCTGGAACAT[A/G]GGAGGCAGAGGTTGC | 197370 |
rs370647494 | snp | C/T | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27260222 | TTTTAAAAAACTAAA[C/T]ACACAAAAATAATAA | 197370 |
rs370721318 | snp | A/C | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27241183 | TGGAACCTAGGATTC[A/C]CTGTGCACTTGGGCA | 197370 |
rs370824600 | snp | C/T | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27232198 | GAGGAAGCGGGGACC[C/T]GGCGTGAGTGCGTCC | 197370 |
rs370825448 | snp | A/G | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27253031 | AAGTAGAGAGGGCAC[A/G]GAAACTCCATGCCAC | 197370 |
rs370825745 | snp | A/G | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | NSMCE1, FLJ21408 | GRCh38.p7 | 16:27270523 | AGGTTGGATCAGAGA[A/G]GAAAGGAGTCAAAGC | 197370 |
rs370830334 | snp | C/T | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27262292 | ACAGAGCCTGAATAG[C/T]GAAAGCAATCCTAAG | 197370 |
rs370830964 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27231273 | GCATTTATTGAGCAG[C/T]TGAGGTGCCAGGCAC | 197370 |
rs370865056 | snp | A/G | 1.65817e-05 | 0.00287933 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27234160 | ATAAGAAGCCCACCC[A/G]ATGGGCAATGGGGAT | 197370 |
rs370877318 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27241961 | AGCTGGATGCAATCA[C/T]GAAAGGATGTGGGCA | 197370 |
rs370980700 | snp | G/T | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27237132 | AGCGAGGAGCTAATC[G/T]TCCCTTTCAGTTAAG | 197370 |
rs370995885 | snp | C/T | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27246118 | AGGCAGATAAGAGAG[C/T]TGACAAAAACAGAAA | 197370 |
rs370999929 | in-del | -/GT | | | intron-variant | NSMCE1, FLJ21408 | GRCh38.p7 | 16:27268470 | GATGTCTGCGTGTGT[-/GT]TGCGGGAGGACATCC | 197370 |
rs371004832 | snp | C/T | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27227686 | AGATGACGTCACTGA[C/T]GCCTGCAAGTCACCC | 197370 |
rs371026891 | snp | C/T | 0.00117235 | 0.0241827 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27257425 | CTGGGAACAGGGAAA[C/T]GGTACTCACGGTCAT | 197370 |
rs371066203 | snp | A/C | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27248299 | CAACAGTAGTATATT[A/C]GAGTTCCAGTTCCTC | 197370 |
rs371140073 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27260180 | TTTAAAAAAAAGTTT[C/T]TAATACCACAGTAAA | 197370 |
rs371191698 | snp | A/C | 1.66846e-05 | 0.00288826 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27232957 | GAAAAAACTGTTATT[A/C]ACTTGAAAAAGTGAA | 197370 |
rs371292856 | snp | A/G | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27236753 | GATACATTCATGTGT[A/G]AAACAAAAACAGAAC | 197370 |
rs371340021 | snp | A/T | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27227750 | TTTTTAATTTTTACA[A/T]GCAAGAGCTGTCACT | 197370 |
rs371355620 | snp | A/C | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27233446 | AGTGAGAGAGAGACA[A/C]GGCAGGCAGGAACCG | 197370 |
rs371404987 | snp | G/T | 4.97649e-05 | 0.00498798 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27234304 | GTCAGGCTGTGCTCT[G/T]TGCGTGTTGGTTAAC | 197370 |
rs371500174 | snp | A/G | 1.66059e-05 | 0.00288144 | synonymous-codon | NSMCE1 | GRCh38.p7 | 16:27225790 | AGCATTCGACTGGAA[A/G]TACTTGGCCACGCAG | 197370 |
rs371565146 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27239717 | ACAGAGGAACGAGGC[C/G/T]CTGGCCCTAGCACAG | 197370 |
rs371662810 | snp | C/T | 8.32328e-05 | 0.00645054 | utr-variant-3-prime | NSMCE1 | GRCh38.p7 | 16:27225151 | CCCCTCAGCAGGGCA[C/T]GATGGCTAATGCTGC | 197370 |
rs371711009 | snp | C/T | 8.29979e-05 | 0.00644143 | missense, utr-variant-5-prime | NSMCE1 | GRCh38.p7 | 16:27235288 | CCTCCAACTTATCTA[C/T]GGTGGCATTGCCTGG | 197370 |
rs371713918 | snp | C/T | 1.65658e-05 | 0.00287795 | synonymous-codon | NSMCE1 | GRCh38.p7 | 16:27233019 | AATCAGCCACTTGTT[C/T]TGAACAAACTTCTGC | 197370 |
rs371749603 | snp | A/G | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27245810 | AGACCGGCTCTGACA[A/G]TGGTATGCTGATTAA | 197370 |
rs371830471 | snp | A/T | 0.000157988 | 0.00888645 | missense, utr-variant-5-prime | NSMCE1 | GRCh38.p7 | 16:27257501 | CTAGCACGCCATGGG[A/T]CATCAGCAACTGGAG | 197370 |
rs371934881 | snp | C/T | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27235741 | TGTCCCTGTATGTCC[C/T]CACACATCTTAGGTG | 197370 |
rs372043380 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27243231 | CAATGCCTGTAAGTT[A/G]TATACCACTGACCGT | 197370 |
rs372047559 | snp | C/T | 3.33706e-05 | 0.00408463 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27225893 | TGGTGCACACCTCCA[C/T]GTTCTGCAAACCTCC | 197370 |
rs372134782 | snp | C/G | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27226039 | CTGCTTGTTGCGGTG[C/G]GTTTTACTAAACAAT | 197370 |
rs372148290 | snp | A/G | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27238433 | TTCCTTCCTCATCAC[A/G]TGGCACTCCAGTTAC | 197370 |
rs372226116 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27249076 | CTCAAGCAATCCACC[A/G]GCTTCAGCCTCCCAG | 197370 |
rs372254379 | snp | C/G | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27239955 | TGATTACCTTATTAT[C/G]TGCCAGCACTATGCA | 197370 |
rs372256213 | snp | A/T | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27264891 | CAAAATACAAAAGAT[A/T]CATATTCAGACTATA | 197370 |
rs372266048 | snp | C/T | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27230068 | AGTCAGGACCTCGTG[C/T]AGGGAGCAGTCCTGG | 197370 |
rs372339891 | in-del | -/A | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27226190 | AGCTTTCAAAAAAAA[-/A]GTGCACTTTGTCCCA | 197370 |
rs372355378 | snp | C/G | 0.000165986 | 0.00910854 | synonymous-codon | NSMCE1 | GRCh38.p7 | 16:27233106 | GTTCAATATGTTTGT[C/G]GAAGACGCAAAGCCG | 197370 |
rs372435541 | snp | A/G | 1.66807e-05 | 0.00288792 | missense | NSMCE1 | GRCh38.p7 | 16:27225740 | CTTGGGATCTCGTGG[A/G]GCCAGTAGTCGTTGC | 197370 |
rs372591135 | snp | A/G | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27237933 | TGCTTGGGCGCTCCC[A/G]TTCTCTCCGCTATCG | 197370 |
rs372596932 | snp | A/G | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27265610 | TTACAGAAGCACCTT[A/G]TAATAACAAAAGTCT | 197370 |
rs372628722 | snp | C/T | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27232846 | TGAGGCCCAAGTCCT[C/T]CCCACGGGGTCACTG | 197370 |
rs372637787 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27251121 | GCTGGGATTACAGGC[A/G]TGAGCTACCGCGCCC | 197370 |
rs372669704 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27250356 | GTCTTTCACCATTAA[A/G]AGTGATGTTAGCTGT | 197370 |
rs372682879 | snp | C/G | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27228940 | GGCCTCCACCCTCTT[C/G]CACCCTCCCCTGCTC | 197370 |
rs372685296 | snp | C/T | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27228762 | CCACCTCTCCAGCCC[C/T]CACCCTCTTCCACCC | 197370 |
rs372743594 | snp | A/G | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27236982 | CAGAAGATCATGCTG[A/G]TGACAATGGAGGATG | 197370 |
rs372888313 | snp | A/G | 0.000437904 | 0.0147905 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27234128 | GCCACTGCTAATGAC[A/G]GAGACAGAACTTTCC | 197370 |
rs373062939 | snp | C/T | 0.000119007 | 0.00771295 | utr-variant-3-prime | NSMCE1 | GRCh38.p7 | 16:27225154 | CTCAGCAGGGCACGA[C/T]GGCTAATGCTGCCTG | 197370 |
rs373089632 | snp | C/T | | | upstream-variant-2KB, intron-variant | NSMCE1, FLJ21408 | GRCh38.p7 | 16:27270325 | ATGGTTCTCCTTGCC[C/T]GCTTCCTAGACAGAA | 197370 |
rs373091896 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27236185 | GTGAGGACAGGAGCC[C/G]GTGGCCGGGGACAGC | 197370 |
rs373106291 | snp | A/G | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27229965 | GTCCTCTGAGGGCCC[A/G]TCAGGGGAGGGGCAG | 197370 |
rs373142283 | snp | A/C | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27246200 | TTGACACATGTATTT[A/C]AGCGACCTGGTTTTT | 197370 |
rs373253320 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27252450 | TGTGGGATTATTTTT[A/C/T]TTAGAGTGTGCCAAA | 197370 |
rs373261235 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NSMCE1, FLJ21408 | GRCh38.p7 | 16:27266490 | GGCGTGGTGGTGCAC[A/G]CCTGTAATCCCAGCT | 197370 |
rs373280983 | snp | C/T | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27230874 | CACAGAGTACAAGCG[C/T]CTGCAGCCACAGCTC | 197370 |
rs373282429 | snp | C/T | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27245670 | GCACTTAATAACTGC[C/T]GGCTGTCAATTCTGT | 197370 |
rs373297972 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NSMCE1, FLJ21408 | GRCh38.p7 | 16:27267739 | AAATATATGCATTTT[C/T]TTTTTTGAGACGGAG | 197370 |
rs373344417 | snp | C/T | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27254052 | TTGCAATTTCAATCA[C/T]TCCTTTGTTTCATAA | 197370 |
rs373419823 | snp | A/G | 0.000648654 | 0.0179974 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27233160 | CAGCTGGAAGAAAGA[A/G]CAGGTATCATGCTCA | 197370 |
rs373455186 | snp | G/T | 1.66782e-05 | 0.0028877 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27226715 | GTGCCCTGCCCTGCG[G/T]GTACCTGGATGAGGA | 197370 |
rs373529578 | snp | A/G | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27235509 | CAACAGATGGAGGGC[A/G]TTGTGAGGCAGGAGG | 197370 |
rs373579764 | snp | C/T | | | intron-variant, upstream-variant-2KB | NSMCE1, FLJ21408 | GRCh38.p7 | 16:27267647 | AAAAAAAAGTCTGAA[C/T]ACCAAAACTTGTTTA | 197370 |
rs373690990 | snp | C/G | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27255042 | GCACCACCACACCCG[C/G]CTAATTTTTGTATTT | 197370 |
rs373696190 | snp | C/T | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27253498 | ATGTCCAGTATTTTA[C/T]ACTTTGTCCATTTTT | 197370 |
rs373704219 | snp | C/T | 0.000165986 | 0.00910854 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27235316 | TGGAAATAAACAGAC[C/T]AAAAAAAGGGGGGTG | 197370 |
rs373732891 | snp | A/C | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27261166 | AGCAAGACTCCGTCT[A/C]AAAAAAAAAAAAAAA | 197370 |
rs374005172 | snp | G/T | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27248401 | CTCACTGCGGTTTTA[G/T]TTTGCTTTTTTTTTT | 197370 |
rs374050262 | snp | C/T | 0.000437904 | 0.0147905 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27234319 | TTGCGTGTTGGTTAA[C/T]GTGTCGCTGGCTCTC | 197370 |
rs374085771 | snp | C/T | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27243807 | AAGCACGAGCCACTA[C/T]GCTCAGCTAACTTTG | 197370 |
rs374090533 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant, utr-variant-5-prime | NSMCE1 | GRCh38.p7 | 16:27241590 | ATCTTTCCCCCAACC[A/G]CCTGGGGAAAAAGAT | 197370 |
rs374172351 | snp | A/G | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27264895 | ATACAAAAGATTCAT[A/G]TTCAGACTATATAAG | 197370 |
rs374254422 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27262180 | ACCTGGGAGGCGGGG[A/G]TTGCAGTGAGCCAAG | 197370 |
rs374265795 | snp | A/C | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27245080 | TGGCAAGTTAAGGGG[A/C]AGAAAAGGAAGGAAG | 197370 |
rs374269798 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27263199 | CCCATTCCTGGGTAT[A/G]TACCAGAGGAACAGA | 197370 |
rs374273906 | snp | A/G | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27232688 | CACACTCTCAGCCAC[A/G]GAACTGCCCTGCCTT | 197370 |
rs374299765 | snp | A/C | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27234975 | ATCCTTGACACTCCT[A/C]CAGAGTTTCTTTTCA | 197370 |
rs374351164 | snp | A/C | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27265322 | TACAGGCACACACCA[A/C]TATGCCCGGCTAATT | 197370 |
rs374383607 | snp | A/G | 8.42538e-05 | 0.00648998 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27225714 | CCCATGAGCTCCTCA[A/G]GGCCCACGCACTTGG | 197370 |
rs374466598 | snp | C/T | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27242421 | TACAATCAGAAAATC[C/T]GCTCTTTAGCCTCAC | 197370 |
rs374471336 | snp | A/G | | | downstream-variant-500B | NSMCE1 | GRCh38.p7 | 16:27224672 | GAGAGCACGCATCCC[A/G]CCCAAACGCCCAGCC | 197370 |
rs374611067 | snp | A/G/T | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27227943 | GGCATGCGCCACCAC[A/G/T]CCTGGCTAATTTTGT | 197370 |
rs374649784 | snp | A/G | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27244265 | TTGGTGCCCATTCTG[A/G]GCTAAGCAGGGGCTA | 197370 |
rs374650230 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27226530 | AGGAGGGCGGCAGTG[C/T]GTCCCTGCGGGGCAC | 197370 |
rs374672673 | snp | A/G | 0.000166218 | 0.0091149 | missense, utr-variant-5-prime | NSMCE1 | GRCh38.p7 | 16:27257536 | CGCCGGTGGACATCA[A/G]TCATGACGCCCATTC | 197370 |
rs374700486 | snp | G/T | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27248691 | TGGGATTACAGGTGT[G/T]AGCCACCATGCCTGG | 197370 |
rs374830712 | snp | A/C | 4.99455e-05 | 0.00499702 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27233162 | GCTGGAAGAAAGAGC[A/C]GGTATCATGCTCATC | 197370 |
rs374833482 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27240530 | CTGGGCCAGGTCCAG[C/T]GTGCAGGGACAGCAT | 197370 |
rs374860424 | snp | C/T | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27237180 | AAATTAAAAAGTAGT[C/T]ATAGTAAGTGGGTGG | 197370 |
rs374863339 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27264283 | GATACTGAGGTGGGA[A/G]GACTGCTTCAGCTCG | 197370 |
rs374975367 | snp | A/G | 0.000165986 | 0.00910855 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27232991 | GGCTGGAAAAACCAT[A/G]AGACAGTACCTCAAT | 197370 |
rs374996966 | snp | A/T | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27234757 | GCTGAGGTGTCTCCT[A/T]GCCAGGGATGGGGCA | 197370 |
rs375192932 | in-del | -/GGCAA | 0.00517822 | 0.0506191 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27240633 | ATGCCCATCAGTGGT[-/GGCAA]GGCAATTGAAAACGG | 197370 |
rs375267676 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | NSMCE1 | GRCh38.p7 | 16:27241861 | TCGCTGCTTCTCTTT[C/T]TCAGAGGTCAGAGAG | 197370 |
rs375321588 | snp | A/G | 3.33506e-05 | 0.0040834 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27226716 | TGCCCTGCCCTGCGG[A/G]TACCTGGATGAGGAG | 197370 |
rs375343470 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27245886 | AAACAGAAGGAAAAT[G/T]TACTTGGAGCCAGCT | 197370 |
rs375343480 | snp | A/G | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27243475 | ACCACGTATAAAAGC[A/G]GAACTCCAACCCAAA | 197370 |
rs375358896 | snp | A/C | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27256619 | TGGCACACAACTCAA[A/C]AATATCTGCCAATGC | 197370 |
rs375369893 | snp | C/T | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27232868 | GGGTCACTGCTGGAA[C/T]GCATGAAAGCAGATA | 197370 |
rs375371533 | snp | A/G | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27237762 | GACACCCCGTTGCAG[A/G]GAGGGAGCCAGCAGC | 197370 |
rs375455550 | in-del | -/A | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27263829 | GACGTCTACAAAAAA[-/A]CCTGCAGCAAACATC | 197370 |
rs375584745 | snp | A/G | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27236511 | CATGTTGGCCAGGCT[A/G]GTCTCGATCTCCTGA | 197370 |
rs375586365 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27259786 | AGATTAAACACAATC[A/C]AAGAAAAAGTCAGAT | 197370 |
rs375586739 | snp | A/C | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27251871 | TTTTCTCTCTGTGCA[A/C]CTCTGGTCCACCTTA | 197370 |
rs375604115 | snp | C/T | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27263713 | TTTTAAAAAAGCATA[C/T]GATCATCTTAATGAT | 197370 |
rs375630897 | in-del | -/T | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27258757 | TGTTCTTTTTTTTTT[-/T]CTTTTTTTTCTGAGA | 197370 |
rs375663140 | snp | A/G | 3.31664e-05 | 0.00407211 | synonymous-codon | NSMCE1 | GRCh38.p7 | 16:27226765 | GATCTTCACCGCGTC[A/G]GGGTACGTCTCCCGG | 197370 |
rs375696361 | snp | A/G | 0.000104288 | 0.00722033 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27226678 | AGAGCCCCGGGAGCC[A/G]AGGGCCCAGTGATGA | 197370 |
rs375705324 | snp | A/C/G | 0.00037632 | 0.0137123 | missense | NSMCE1 | GRCh38.p7 | 16:27225191 | AGGGACTTTTTGTTC[A/C/G]ATTTCAAGACACCAG | 197370 |
rs375742311 | snp | C/T | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27230576 | AAACAGTCTCCGCAA[C/T]GAGAAGCTGCTCACC | 197370 |
rs375891217 | snp | C/T | 0.000161987 | 0.00899818 | missense | NSMCE1 | GRCh38.p7 | 16:27225750 | CGTGGGGCCAGTAGT[C/T]GTTGCAGTGGGGGCA | 197370 |
rs375935708 | snp | C/T | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27236748 | AATATGATACATTCA[C/T]GTGTGAAACAAAAAC | 197370 |
rs375982815 | snp | A/G | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27251714 | TCAAATGTTTGGGCC[A/G]GGCACTATTCCCAGT | 197370 |
rs376000854 | snp | C/G | 1.65608e-05 | 0.00287752 | missense | NSMCE1 | GRCh38.p7 | 16:27233067 | CTTCTTCCTCATCTT[C/G]TTGCCTTTAAGTTGA | 197370 |
rs376018814 | snp | A/G | | | upstream-variant-2KB, intron-variant | NSMCE1, FLJ21408 | GRCh38.p7 | 16:27270344 | TCCTAGACAGAACCA[A/G]TTTATCAAGACAGGG | 197370 |
rs376020495 | snp | A/C | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27244497 | GCTCCATCCCCTGAC[A/C]TATGTTGCCACCTGC | 197370 |
rs376094904 | snp | C/T | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27234760 | GAGGTGTCTCCTAGC[C/T]AGGGATGGGGCATGT | 197370 |
rs376132943 | snp | A/C | 1.71047e-05 | 0.00292439 | splice-donor-variant | NSMCE1 | GRCh38.p7 | 16:27257433 | AGGGAAACGGTACTC[A/C]CGGTCATGGACCTTG | 197370 |
rs376139353 | snp | C/G | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27226615 | GAGGATGCGCCAGCA[C/G]TGCAGGAGGGCTGGG | 197370 |
rs376178703 | snp | C/T | 4.98401e-05 | 0.00499175 | missense | NSMCE1 | GRCh38.p7 | 16:27226808 | ATCTCCAGGATGGCC[C/T]GGCCGTGCAGGGTGA | 197370 |
rs376184990 | snp | A/G | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27252913 | GACAAGAGCAAAACT[A/G]TCTCAAAAAAAATAA | 197370 |
rs376228768 | snp | C/G | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27225506 | GACAAAATGCTCATA[C/G]ACGTTGGAATTTCAG | 197370 |
rs376325690 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27246203 | ACACATGTATTTCAG[C/T]GACCTGGTTTTTGCC | 197370 |
rs376327797 | snp | C/T | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27227651 | AGTCAGCTCATGCAT[C/T]GGATATGAACCACAC | 197370 |
rs376561538 | snp | A/G | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27246058 | TGAGACGACGAAGCA[A/G]ATACAGGCATGTCAA | 197370 |
rs376627089 | snp | A/G | 6.63196e-05 | 0.00575807 | missense, utr-variant-5-prime | NSMCE1 | GRCh38.p7 | 16:27235182 | CGGGCACTCACCAAC[A/G]CATAAATGGGTCTCC | 197370 |
rs376639108 | snp | A/G | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27257178 | GCTGGGGCAGGTCCT[A/G]GAGGCTTGGTGTGAA | 197370 |
rs376700395 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | NSMCE1, FLJ21408 | GRCh38.p7 | 16:27269646 | ATGGGAGTGCTGATT[A/G]TATGTTAACTGTTAT | 197370 |
rs376793328 | snp | C/T | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27236207 | GGGGACAGCAGGGCC[C/T]TTCTCCTGTGGCACC | 197370 |
rs377069907 | snp | C/T | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27249121 | AGGTGTGAGCCACCA[C/T]GCCCAGCCGGGTTGA | 197370 |
rs377074596 | snp | C/T | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27228488 | CCCTGGCCACCGCCC[C/T]CTTCCAGCCTCCCCT | 197370 |
rs377106243 | snp | A/T | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27239956 | GATTACCTTATTATG[A/T]GCCAGCACTATGCAT | 197370 |
rs377115489 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27236180 | CTGCGGTGAGGACAG[A/G]AGCCCGTGGCCGGGG | 197370 |
rs377117969 | snp | C/T | 8.29511e-05 | 0.00643962 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27234153 | CTTTCCCATAAGAAG[C/T]CCACCCAATGGGCAA | 197370 |
rs377174369 | snp | C/T | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27226425 | CTCACTACAAAACTA[C/T]CAAGATGATGCAGGT | 197370 |
rs377206133 | snp | A/G | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27226941 | CTCAGGAAGACACAA[A/G]GGTCTACGCAGCTTT | 197370 |
rs377278049 | snp | C/T | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27250934 | GCAACCTCTGCCTCC[C/T]GGATTCAAGCAATTC | 197370 |
rs377283141 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27232699 | CCACGGAACTGCCCT[A/G]CCTTGCAGTCTGTGG | 197370 |
rs377418919 | snp | A/G | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27258896 | GCTGGAACTACAGGC[A/G]CCCACCACCGTGCCT | 197370 |
rs377451020 | snp | A/G | 1.72892e-05 | 0.00294012 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27257419 | AGCGCCCTGGGAACA[A/G]GGAAACGGTACTCAC | 197370 |
rs377478563 | snp | A/C | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27240478 | CTCAACCCAGCCCAC[A/C]CCAGCATCCATCATC | 197370 |
rs377559774 | snp | C/T | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27248406 | TGCGGTTTTAGTTTG[C/T]TTTTTTTTTTTTTTT | 197370 |
rs377576067 | snp | A/C | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27261622 | AATGACTTTATCAAG[A/C]AGTTCTACCAAATAG | 197370 |
rs377576865 | snp | A/C | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27236453 | AGGCATGCACCACCA[A/C]ACCCAGCTAATTTTT | 197370 |
rs377634453 | snp | A/C | 0.00081195 | 0.0201325 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27234284 | AGAAATAAGTCAGCA[A/C]GACAGTCAGGCTGTG | 197370 |
rs377649978 | snp | A/G | 3.34465e-05 | 0.00408927 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27235321 | ATAAACAGACCAAAA[A/G]AAGGGGGGTGACCAG | 197370 |
rs377742883 | snp | A/C | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27239452 | ATGGTCATGATAAAG[A/C]GTGCGGAATAAAGTC | 197370 |
rs377762617 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27243943 | GGCATGTACCACCAT[A/G]CTTGCCAGCTTCCCT | 197370 |
rs377765458 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27231332 | AGAGGTCATAACCCC[A/T]ACCCTTAAAAAACTT | 197370 |
rs386384556 | in-del | -/CAGC | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27239959 | ACCTTATTATGTGCC[-/CAGC]AGCACTATGCATTCA | 197370 |
rs386790132 | multinucleotide-polymorphism | CA/TG | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27231529 | GTGATTCCAGCTACT[CA/TG]GGAGGCTGAGGCAGG | 197370 |
rs397744800 | in-del | -/TGTA | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27226255 | AAGGATACAGGTGTA[-/TGTA]CGAGGCCCGTAAGAG | 197370 |
rs397759295 | in-del | -/CT | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27237639 | AAGTCCCACCTCTCT[-/CT]GAAAGTGACAATTCA | 197370 |
rs397777076 | in-del | -/A | 0 | 0 | intron-variant, upstream-variant-2KB | NSMCE1, FLJ21408 | GRCh38.p7 | 16:27266632 | AAAAGAAAAAAAAAA[-/A]TTACTTTTTTTAAAA | 197370 |
rs397971855 | in-del | -/T | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27251208 | ATATATATATATATA[-/T]AAACTCTGTAGAGTT | 197370 |
rs398058186 | in-del | -/ACT | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27236645 | ATTATTGTTTTCACT[-/ACT]GTTTTTATGTATTAA | 197370 |
rs527284272 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27229904 | TACTGAACACCTGCT[A/G]TGTGCCTGAAACTGC | 197370 |
rs527310921 | snp | C/T | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27243847 | CAGACCCTGAGGTCT[C/T]GCAATGTTGCCCAGG | 197370 |
rs527724327 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27250784 | GGAGGCTTTTTTGAG[A/G]CTCTCTCTCAAAAAT | 197370 |
rs527742544 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27250258 | CCTTTTGTTTCTTTT[A/T]CTCGCCTCAGTACAC | 197370 |
rs527773254 | snp | C/T | | | intron-variant, upstream-variant-2KB | NSMCE1, FLJ21408 | GRCh38.p7 | 16:27267397 | AAGGGTCACTGACCC[C/T]ATCTTACAGATGAGG | 197370 |
rs527799510 | snp | A/G | 0.000101835 | 0.00713491 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27257587 | TGGGAACGAACTGAA[A/G]AGGAAGTAAATGACA | 197370 |
rs527806313 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NSMCE1, FLJ21408 | GRCh38.p7 | 16:27266571 | GCAGTGAGCCAAGAT[A/C]GCGTCACTGCACTCT | 197370 |
rs527813574 | snp | C/T | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27237348 | CCTCTCCCTCCACTG[C/T]GGCAGCCACCTTGGA | 197370 |
rs527879932 | snp | A/G | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27256747 | TTTGCCCCTCCCAGT[A/G]GCCCCGTAAGATGCC | 197370 |
rs527888767 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27237401 | TTCTCTTCTGCCCCC[A/G]GTGCTGTCTTCCTCT | 197370 |
rs527901682 | snp | A/G | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27235859 | AGAATAACAACAAAC[A/G]GGGTGAGAAGGGTGG | 197370 |
rs527947896 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27244365 | TCACTACAGTCTGAA[A/G]CAGACAACAGCCTCC | 197370 |
rs528106453 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMCE1, FLJ21408 | GRCh38.p7 | 16:27268601 | GACCGACCCCGGGGC[A/C]GGACCCCACTGCCTG | 197370 |
rs528129449 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27259564 | CCTCTTTGGCATCAT[A/G]GAGGTGTAGAGGAAA | 197370 |
rs528226720 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27225561 | GCGGTGCACGTAGCT[C/T]AGCCTTTACTTCCTG | 197370 |
rs528550077 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27238660 | GACCAGAGATTAGGG[A/C]AGCCAGGAGTAGACA | 197370 |
rs528645504 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27249830 | AACTGGGATTTCTTT[A/C/G]AATCTATAGATCAAT | 197370 |
rs528714865 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27262179 | AACCTGGGAGGCGGG[A/G]GTTGCAGTGAGCCAA | 197370 |
rs528759449 | in-del | -/TATATATAAATATATATATATAT | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27251183 | ATATATATATATATA[-/TATATATAAATATATATATATAT]ATAAAACTCTGTAGA | 197370 |
rs528776359 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | NSMCE1, FLJ21408 | GRCh38.p7 | 16:27270057 | ACAAAGTACAGTCAG[C/T]TGTCCATGTTTACAG | 197370 |
rs528791328 | snp | C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | NSMCE1, FLJ21408 | GRCh38.p7 | 16:27269449 | CTCTGTGGTCATAGA[C/G]CCTGATCTAGAATCC | 197370 |
rs528871215 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27233360 | CACTTCTATAACATC[C/T]TCCCAAATAAATCAT | 197370 |
rs528917816 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27254726 | GGGTAGCTAGGACCA[C/T]AGGTGTGTGCCAGCA | 197370 |
rs528988667 | snp | A/G | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27247092 | TGTAAAATACATATT[A/G]GATTGCAAAGACATA | 197370 |
rs528993638 | snp | C/T | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27263542 | ACACTGGGGTCTATT[C/T]GAGGATGGAGGGTGG | 197370 |
rs529089334 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27229027 | GGCCCTGTCACTCCC[A/G]ACTCACCCCCACCCC | 197370 |
rs529158593 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | NSMCE1 | GRCh38.p7 | 16:27241439 | GCAGGCCCTGGATGA[C/G]ACGGGGGTGCAGGAG | 197370 |
rs529359260 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27263950 | AGAGGCTTTGTGTAT[A/G]TGTGTGTGTGATTTG | 197370 |
rs529441556 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27235882 | AAGGGTGGCTTGCAG[C/T]GAGCCCTCAGCATGG | 197370 |
rs529497497 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27243072 | CAGCAGGGAGCTGGC[A/G]GCACGCATTCTACCA | 197370 |
rs529511067 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27242205 | TCAACAATCATATAA[C/T]TTGACTCCTTGACCC | 197370 |
rs529543016 | snp | A/G | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27255452 | ACACGAAAAGAATGT[A/G]TTCTCTTCCCACACA | 197370 |
rs529561934 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27250020 | TCTTATTTTTAATGT[C/T]ATTATAAATGGTGCT | 197370 |
rs529573964 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27240886 | AAGACAAGCCTGAGC[-/A]ATGGATCAAGAGCTC | 197370 |
rs529596391 | snp | A/G | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27230383 | GTGGTCTCTCTGATC[A/G]AGGTGCTGCCCTAGG | 197370 |
rs529613865 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27256970 | TATCCTCCCACCTTG[A/G]TTCCCAGAGTGCAGG | 197370 |
rs529694136 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27230500 | GCCATGTAGGTCAGA[A/G]AGCACTGGACCCTCA | 197370 |
rs529949607 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27265764 | AAGATAATGTTAAGT[G/T]CAACAAGCAAGTCAC | 197370 |
rs529978617 | snp | A/C | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27225311 | CCAGCTGGAGCCAGC[A/C]GCTACGTCTCCTGTG | 197370 |
rs529992898 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NSMCE1, FLJ21408 | GRCh38.p7 | 16:27266591 | CACTGCACTCTAGCC[C/T]GGGCGACAGGGCGAG | 197370 |
rs530074827 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27244523 | CCTGCCTTTCTGTCC[C/T]CCACTCCCCCACACC | 197370 |
rs530087314 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27243858 | GTCTCGCAATGTTGC[C/T]CAGGCTGGTCTCAAA | 197370 |
rs530092635 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27237474 | GCTGTTCCGTACCTG[C/T]CTGTGCCAGTGACTT | 197370 |
rs530141807 | snp | A/G | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27263659 | GACGTGAGTTTACCT[A/G]TCTAATAAACCTTCA | 197370 |
rs530149501 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27251030 | ATTTTTAGTAGAGAC[A/G]GGGTTTCTCCATGTT | 197370 |
rs530170807 | snp | A/T | | | intron-variant | NSMCE1 | GRCh38.p7 | 16:27249277 | TTTTTTAATGTAAAT[A/T]TTTAATTGTGAAGTT | 197370 |
rs530209617 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27247344 | CCTGCCACCATGTGA[A/G]GAAGGATGTGTTTGC | 197370 |
rs530305579 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27226434 | AAACTACCAAGATGA[C/T]GCAGGTTGCACAGAA | 197370 |
rs530382251 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27231598 | GCCAAGATTGCACCA[C/T]TGCACTCCAGCCTGG | 197370 |
rs530450413 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27260748 | TCCGTAGTCCCAGCT[A/G]TTTAGGAGGCTGAGG | 197370 |
rs530514801 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | NSMCE1, FLJ21408 | GRCh38.p7 | 16:27269258 | ACCCCCGTCCCTACT[A/G]AAAATACAAAAAGTA | 197370 |
rs530526173 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NSMCE1, FLJ21408 | GRCh38.p7 | 16:27268643 | CCACCTTCCGTCCTC[C/T]CCTCGCCTTCCTTGA | 197370 |
rs530617365 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27260056 | AAGGGATACAAGTTG[A/G]AAGGTCTAAAATGCA | 197370 |
rs530730440 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27253000 | TAAACACACAGAGGC[A/G]TTGAGACGGTGGTGC | 197370 |
rs530765289 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE1 | GRCh38.p7 | 16:27238853 | CCTATGTGTCCCTCC[C/G]CCAATAGCATCCCGA | 197370 |