SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs14852 | snp | A/G | 0 | 0 | utr-variant-3-prime | MNAT1 | GRCh38.p7 | 14:60968589 | TAGCCTCATCTGATG[A/G]AAGAGAGGAATAAAT | 4331 |
rs752571 | snp | A/C | 0.242201 | 0.249878 | intron-variant | MNAT1 | GRCh38.p7 | 14:60905626 | GTCTCCATTCTCAGG[A/C]CTTCAACCTCAAACT | 4331 |
rs753014 | snp | A/G | 0.232651 | 0.249397 | intron-variant | MNAT1 | GRCh38.p7 | 14:60904862 | TACTTCTCCCGTATC[A/G]TGGTAGAATTCAGTA | 4331 |
rs913482 | snp | C/T | 0.232359 | 0.249377 | intron-variant | MNAT1 | GRCh38.p7 | 14:60906942 | ggagcttggggatga[C/T]tgtaaaactcaaagt | 4331 |
rs913483 | snp | A/C | 0.197393 | 0.244402 | intron-variant | MNAT1 | GRCh38.p7 | 14:60904541 | TGTTGATGAAAGAAG[A/C]TTGTTTGACAACTGC | 4331 |
rs958015 | snp | G/T | 0.0138799 | 0.0821421 | intron-variant | MNAT1 | GRCh38.p7 | 14:60822831 | ggacagaggttgcag[G/T]gagtccagattgtgt | 4331 |
rs958016 | snp | C/T | 0.191147 | 0.242974 | intron-variant | MNAT1 | GRCh38.p7 | 14:60822793 | ctccagcctggtcga[C/T]agaccaagactccat | 4331 |
rs972758 | snp | A/G | 0.283947 | 0.247685 | intron-variant | MNAT1 | GRCh38.p7 | 14:60941990 | TTGAGATGGAGCCTC[A/G]TTCTGTCGCCCAGGC | 4331 |
rs973063 | snp | C/T | 0.472709 | 0.11358 | intron-variant | MNAT1 | GRCh38.p7 | 14:60818634 | ATTATGTCTTTTCCA[C/T]AAGCATTTCATGTCA | 4331 |
rs975182 | snp | C/T | 0.29432 | 0.24604 | intron-variant | MNAT1 | GRCh38.p7 | 14:60943772 | ATACCTTGCATAAAT[C/T]TGAAAACTTAAAATG | 4331 |
rs1013670 | snp | A/G | 0.211819 | 0.247067 | intron-variant | MNAT1 | GRCh38.p7 | 14:60827039 | TCAGTTTGCAAACAA[A/G]CAAAATAGAATGAAG | 4331 |
rs1028897 | snp | A/T | 0.308661 | 0.24302 | intron-variant | MNAT1 | GRCh38.p7 | 14:60966489 | AATATTTTCTCCATA[A/T]ACTGTATCTTACATA | 4331 |
rs1028898 | snp | A/G | 0.278664 | 0.248351 | intron-variant | MNAT1 | GRCh38.p7 | 14:60966439 | ACTTTAGAGACTACT[A/G]TTATTAATTAGTCAT | 4331 |
rs1033738 | snp | G/T | 0.0103295 | 0.0711199 | intron-variant | MNAT1 | GRCh38.p7 | 14:60758607 | TTTCTGAATTTGGGG[G/T]TTTTTTTTTGGAGGG | 4331 |
rs1051083 | snp | A/C | 0 | 0 | utr-variant-3-prime | MNAT1 | GRCh38.p7 | 14:60968610 | AGGAATAAATAATTC[A/C]CCTATATGTGTTTGA | 4331 |
rs1115839 | snp | A/C | | | intron-variant | MNAT1 | GRCh38.p7 | 14:60846747 | ggccataacataagt[A/C]acggtaaattttaaa | 4331 |
rs1116402 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | MNAT1 | GRCh38.p7 | 14:60884628 | ataaatagaacaaca[A/G]aaagttaaaaagcaa | 4331 |
rs1475020 | snp | C/T | 0.329317 | 0.237084 | intron-variant | MNAT1 | GRCh38.p7 | 14:60792782 | CAGAATGACATCCTT[C/T]TTCTCTCTGAATGAC | 4331 |
rs1475456 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MNAT1 | GRCh38.p7 | 14:60896876 | TCAACACTTTGCCAA[C/T]AAGTCTTTTTTTTTT | 4331 |
rs1536713 | snp | A/C | 0.102014 | 0.201495 | intron-variant | MNAT1 | GRCh38.p7 | 14:60929386 | TTACAGGAAAACATA[A/C]GAGGAAATCTTCTTG | 4331 |
rs1571388 | snp | G/T | 0.328382 | 0.237395 | intron-variant | MNAT1 | GRCh38.p7 | 14:60935827 | AGCTTGATGTTCAAT[G/T]TCCTTATCTACAGGG | 4331 |
rs1571389 | snp | C/T | 0.197082 | 0.244335 | intron-variant | MNAT1 | GRCh38.p7 | 14:60880557 | CCCACTTTTTTTTCA[C/T]AGTATATTCTTTCCA | 4331 |
rs1571390 | snp | A/G | 0.258288 | 0.249863 | intron-variant | MNAT1 | GRCh38.p7 | 14:60850615 | GTAAGGTTATTCCAA[A/G]CATGAATAAGGTTAT | 4331 |
rs1801614 | snp | A/G | | | intron-variant | MNAT1 | GRCh38.p7 | 14:60780406 | GGTGACATTTCTGCC[A/G]CTGTTGGAAGTTTCT | 4331 |
rs1885093 | snp | A/C | 0.230896 | 0.249269 | intron-variant | MNAT1 | GRCh38.p7 | 14:60752509 | AAATAAGAAGATAAA[A/C]ATTAAAAGAACTCCT | 4331 |
rs1887741 | snp | C/T | 0.191775 | 0.243125 | intron-variant | MNAT1 | GRCh38.p7 | 14:60867942 | CACACAATTTCATGG[C/T]AAGTATAATTCATTT | 4331 |
rs1951108 | snp | C/T | 0.32955 | 0.237006 | intron-variant | MNAT1 | GRCh38.p7 | 14:60751521 | CTAGTTGACATCTGA[C/T]TATACCTCAAAAACC | 4331 |
rs1951110 | snp | A/G | 0.230017 | 0.2492 | intron-variant | MNAT1 | GRCh38.p7 | 14:60778033 | ACCCACTATCACCAA[A/G]TTAGACCCAGCACAG | 4331 |
rs1951111 | snp | C/T | | | intron-variant | MNAT1 | GRCh38.p7 | 14:60773660 | GTTCTTTCTGACTTT[C/T]TGAATGGGGCAGTTT | 4331 |
rs1952401 | snp | A/T | | | intron-variant | MNAT1 | GRCh38.p7 | 14:60869042 | AAAAAAAAAAAAAAA[A/T]ATATATATATATATA | 4331 |
rs1952402 | snp | C/G | 0.116138 | 0.211142 | intron-variant | MNAT1 | GRCh38.p7 | 14:60868323 | TCAATTGAAGTAATT[C/G]TGAATGACTATTTCT | 4331 |
rs1952404 | snp | C/T | 0.030665 | 0.119967 | intron-variant | MNAT1 | GRCh38.p7 | 14:60949235 | CCCGCTACAATTAGT[C/T]AACAGGAAGTAAAGA | 4331 |
rs1952405 | snp | A/G | | | intron-variant | MNAT1 | GRCh38.p7 | 14:60948936 | CTGGAAGGAAATTTT[A/G]AAATCATCTTATCTT | 4331 |
rs1956866 | snp | C/T | 0 | 0 | intron-variant | MNAT1 | GRCh38.p7 | 14:60759537 | CTCATCAACTCCATG[C/T]TGTTGAGAATATGGA | 4331 |
rs1956867 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | MNAT1 | GRCh38.p7 | 14:60829104 | tccaccaacctctgg[A/G]aagaggtgaggggca | 4331 |
rs1956868 | snp | C/T | 0.243919 | 0.249926 | intron-variant | MNAT1 | GRCh38.p7 | 14:60764770 | AGCTACTACCATTTG[C/T]TAATTTATTTATTTG | 4331 |
rs1956869 | snp | C/T | 0.188946 | 0.24243 | intron-variant | MNAT1 | GRCh38.p7 | 14:60764676 | AATTACATTCTTCAC[C/T]TGGGCATCAAAATCC | 4331 |
rs1958277 | snp | A/G | 0.233235 | 0.249437 | intron-variant | MNAT1 | GRCh38.p7 | 14:60892024 | ATTTTTAAAAAATTG[A/G]TATCATACAAAGTAT | 4331 |
rs1958278 | snp | G/T | 0.232651 | 0.249397 | intron-variant | MNAT1 | GRCh38.p7 | 14:60891829 | aagccataccaaaac[G/T]tatgggacacagcaa | 4331 |
rs1958279 | snp | C/T | 0.464523 | 0.128375 | intron-variant | MNAT1 | GRCh38.p7 | 14:60883755 | actataaaatactga[C/T]gcaaaaaattgaaga | 4331 |
rs1958282 | snp | C/T | 0 | 0 | intron-variant | MNAT1 | GRCh38.p7 | 14:60963531 | ATTTACATTAACAAC[C/T]TGAAGCCTACCTCAG | 4331 |
rs1958283 | snp | A/G | 0.278664 | 0.248351 | intron-variant | MNAT1 | GRCh38.p7 | 14:60947669 | TTCAGATAGAGTCTC[A/G]CTTTGTTGCCGAGGC | 4331 |
rs1958284 | snp | C/T | 0.215446 | 0.2476 | intron-variant | MNAT1 | GRCh38.p7 | 14:60928428 | aaaacagtttggcag[C/T]ttctgaaaagttaaa | 4331 |
rs1963207 | snp | A/C | 0 | 0 | intron-variant | MNAT1 | GRCh38.p7 | 14:60832581 | TTTTGATTACTGTAG[A/C]CTTGTAGTATTGTTT | 4331 |
rs1964900 | snp | C/G | 0.278664 | 0.248351 | intron-variant | MNAT1 | GRCh38.p7 | 14:60966547 | ccagcctgggtgaca[C/G]agcgagactccatct | 4331 |
rs1964901 | snp | C/G | 0.232651 | 0.249397 | intron-variant | MNAT1 | GRCh38.p7 | 14:60903966 | gagaattgcttgaac[C/G]tgggaggcagaagtt | 4331 |
rs1980896 | snp | G/T | 0.276267 | 0.248616 | intron-variant | MNAT1 | GRCh38.p7 | 14:60964560 | AAATATGTGTAAATC[G/T]TATAAGCAGAAACCA | 4331 |
rs1986118 | snp | A/G | 0 | 0 | intron-variant | MNAT1 | GRCh38.p7 | 14:60826316 | aaaaaaaaaaaaaaa[A/G]aaaaaaaaTTTCTCC | 4331 |
rs1999054 | snp | C/T | 0.226484 | 0.248892 | intron-variant | MNAT1 | GRCh38.p7 | 14:60902912 | AAAAACCCAGATATT[C/T]ACCTAATAGAACTAG | 4331 |
rs2020890 | snp | C/T | 0.0433309 | 0.140669 | intron-variant | MNAT1 | GRCh38.p7 | 14:60818699 | TTTTTACATTTCTTA[C/T]TGAACTTGAACTATT | 4331 |
rs2020891 | snp | C/T | 0.277778 | 0.248452 | synonymous-codon, utr-variant-5-prime | MNAT1 | GRCh38.p7 | 14:60734917 | TATCGGAACCCCTCC[C/T]TGAAGCTGATGGTGA | 4331 |
rs2020892 | snp | A/G | 0.432891 | 0.170444 | intron-variant | MNAT1 | GRCh38.p7 | 14:60811966 | AATTTATTCCACGCC[A/G]TATATAAATTTTTGT | 4331 |
rs2025966 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | MNAT1 | GRCh38.p7 | 14:60924563 | CATATTATTGTTTCT[C/T]CATTTTAAAAGTAGA | 4331 |
rs2025967 | snp | A/G | 0.459574 | 0.136304 | intron-variant | MNAT1 | GRCh38.p7 | 14:60866645 | TATTTGTGGTCACAT[A/G]CAATTACTTTTGAGA | 4331 |
rs2057318 | snp | C/T | 0.188 | 0.24219 | intron-variant | MNAT1 | GRCh38.p7 | 14:60764169 | AGATATATCATACCA[C/T]TAACAAATATTACAT | 4331 |
rs2057319 | snp | A/C | 0.188 | 0.24219 | intron-variant | MNAT1 | GRCh38.p7 | 14:60764162 | TCATACCACTAACAA[A/C]TATTACATAACACTC | 4331 |
rs2057320 | snp | G/T | 0 | 0 | upstream-variant-2KB | MNAT1 | GRCh38.p7 | 14:60733870 | CTTTTCAATAAAAAG[G/T]AATATTCAATTCACA | 4331 |
rs2057321 | snp | C/T | 0.186421 | 0.24178 | upstream-variant-2KB | MNAT1 | GRCh38.p7 | 14:60733867 | TTCAATAAAAAGTAA[C/T]ATTCAATTCACATTT | 4331 |
rs2093250 | snp | A/T | 0.460027 | 0.135605 | intron-variant | MNAT1 | GRCh38.p7 | 14:60855935 | ggagaaggagagaga[A/T]gagagatggggcaat | 4331 |
rs2093251 | snp | A/G | 0.460365 | 0.13508 | intron-variant | MNAT1 | GRCh38.p7 | 14:60855853 | tgggtgtggttcctg[A/G]cagcctaaaacaatt | 4331 |
rs2094552 | snp | A/G | 0.241914 | 0.249869 | intron-variant | MNAT1 | GRCh38.p7 | 14:60905957 | TACTAATTATCATAT[A/G]Gaattttatgtgtca | 4331 |
rs2104075 | snp | A/T | 0.188946 | 0.24243 | intron-variant | MNAT1 | GRCh38.p7 | 14:60826025 | TTGAACCCTTCAACT[A/T]TCTCTAGGTTTATTA | 4331 |
rs2104654 | snp | A/C | 0.287867 | 0.247116 | intron-variant | MNAT1 | GRCh38.p7 | 14:60956039 | GCCCAAAGTTACAGT[A/C]AGGATGGAAATAAAG | 4331 |
rs2145537 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | MNAT1 | GRCh38.p7 | 14:60828387 | TTATAAGTCACAAAC[C/T]CTACCTTCAATCACA | 4331 |
rs2145538 | snp | G/T | 0 | 0 | intron-variant | MNAT1 | GRCh38.p7 | 14:60828362 | ATCACAATTTACTGG[G/T]CTATTATAGTTTTTA | 4331 |
rs2149301 | snp | C/G | 0.192088 | 0.2432 | intron-variant | MNAT1 | GRCh38.p7 | 14:60880472 | TTCACATTTTAAAAT[C/G]AGACCAAGAAATGAT | 4331 |
rs2149304 | snp | C/T | 0.314787 | 0.241459 | intron-variant | MNAT1 | GRCh38.p7 | 14:60958127 | agtatagagtgggca[C/T]ggtggctcaagcctg | 4331 |
rs2149305 | snp | C/T | 0.481856 | 0.0935034 | intron-variant | MNAT1 | GRCh38.p7 | 14:60958084 | tttgggagggtgagg[C/T]gggcagatcacctga | 4331 |
rs2149306 | snp | A/G | 0 | 0 | intron-variant | MNAT1 | GRCh38.p7 | 14:60944704 | AAATTTTATAATTTA[A/G]GCACTTCTTGTATAT | 4331 |
rs2209895 | snp | A/G | 0.232359 | 0.249377 | intron-variant | MNAT1 | GRCh38.p7 | 14:60905105 | agtaggcacttcata[A/G]ctatttgctaaCCGA | 4331 |
rs2209896 | snp | C/T | 0.241627 | 0.24986 | intron-variant | MNAT1 | GRCh38.p7 | 14:60900810 | tgcccaggctgctct[C/T]gaactcttgggctca | 4331 |
rs2225199 | snp | C/T | 0.232359 | 0.249377 | intron-variant | MNAT1 | GRCh38.p7 | 14:60905092 | TAACTATTTGCTAAC[C/T]GACAACCAAATGAAT | 4331 |
rs2268414 | snp | A/G | 0.0861826 | 0.188849 | intron-variant | MNAT1 | GRCh38.p7 | 14:60761087 | AACAAAGAAGTAAAC[A/G]CATTACATATTAATA | 4331 |
rs2277505 | snp | A/C | 0.00076321 | 0.0195198 | intron-variant | MNAT1 | GRCh38.p7 | 14:60879689 | AAATGAAGGAACTTA[A/C]TACCTCTTATTATTA | 4331 |
rs2284702 | snp | A/G | 0.33875 | 0.233717 | intron-variant | MNAT1 | GRCh38.p7 | 14:60807159 | TCAGAACATCAATTT[A/G]TCATAATCACTGTTG | 4331 |
rs2284703 | snp | A/C | 0.190205 | 0.242744 | intron-variant | MNAT1 | GRCh38.p7 | 14:60806830 | TTTACCAACCACTCA[A/C]AATCTACCTCTTGTA | 4331 |
rs2284704 | snp | A/G | 0.250168 | 0.25 | intron-variant | MNAT1 | GRCh38.p7 | 14:60745150 | GGCAACAATTGCCAT[A/G]ACCATGGCCCAGCAA | 4331 |
rs2300466 | snp | C/T | 0.317692 | 0.240661 | intron-variant | MNAT1 | GRCh38.p7 | 14:60805420 | gtaaactacagactt[C/T]gtgtgataatgatat | 4331 |
rs2300467 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MNAT1 | GRCh38.p7 | 14:60804941 | TTCAAAACAGTTTAA[A/G]AAACACTGTTTATTA | 4331 |
rs2300468 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | MNAT1 | GRCh38.p7 | 14:60804595 | CAAGCTACAGCGAGC[C/T]ATGATAGTACCACTG | 4331 |
rs2300469 | snp | C/T | 0.192401 | 0.243274 | intron-variant | MNAT1 | GRCh38.p7 | 14:60804365 | AAAGAACCATAAAAG[C/T]GAATTACTATTTTAA | 4331 |
rs2300470 | snp | A/T | 0.231189 | 0.249291 | intron-variant, utr-variant-5-prime | MNAT1 | GRCh38.p7 | 14:60799701 | TATATATATATATAT[A/T]TTTTTTTAATCATAG | 4331 |
rs2300471 | snp | A/G | 0.190833 | 0.242898 | intron-variant | MNAT1 | GRCh38.p7 | 14:60797351 | AGTCTAAAAAATACT[A/G]GATCAAGAAAATCTG | 4331 |
rs2300472 | snp | A/T | 0.200492 | 0.245049 | intron-variant | MNAT1 | GRCh38.p7 | 14:60797333 | TCAAGAAAATCTGTA[A/T]ATATTGTAATGTACC | 4331 |
rs2300473 | snp | A/T | 0.21695 | 0.247806 | intron-variant | MNAT1 | GRCh38.p7 | 14:60796981 | TATACACACATATAT[A/T]TACTATGCCCATGTG | 4331 |
rs2351273 | snp | C/T | 0.216048 | 0.247684 | intron-variant | MNAT1 | GRCh38.p7 | 14:60741794 | attacaagagtgagc[C/T]gctgtacctggccCc | 4331 |
rs2351274 | snp | A/T | | | intron-variant | MNAT1 | GRCh38.p7 | 14:60773598 | ATTACTTCAGGCAAT[A/T]ACAGGCGGACAAACC | 4331 |
rs2351277 | snp | A/C | 0.251695 | 0.250295 | intron-variant | MNAT1 | GRCh38.p7 | 14:60787392 | GCTAACAATCATCTG[A/C]GCCTTCGAAAGTGAC | 4331 |
rs2351278 | snp | C/G | 0.250168 | 0.25 | intron-variant | MNAT1 | GRCh38.p7 | 14:60788132 | tcaatgtcagaatta[C/G]tccttgacccatggg | 4331 |
rs2351279 | snp | C/T | 0.230017 | 0.2492 | intron-variant | MNAT1 | GRCh38.p7 | 14:60820658 | CCACCTCTTATCATC[C/T]TAGGATAATTGCCAT | 4331 |
rs2351280 | snp | A/G | 0.18989 | 0.242666 | intron-variant | MNAT1 | GRCh38.p7 | 14:60856578 | tttgtagctaaagag[A/G]agaagtcaatgcccg | 4331 |
rs2351281 | snp | A/G | 0.197082 | 0.244335 | intron-variant | MNAT1 | GRCh38.p7 | 14:60880820 | AAAGTCCTACAGCCT[A/G]CAAGCATGAAGCCAA | 4331 |
rs2351536 | snp | G/T | | | intron-variant | MNAT1 | GRCh38.p7 | 14:60904994 | TTTTTTTTTTTTTTT[G/T]GACGGAGTCTCGCTC | 4331 |
rs2351537 | snp | C/G | 0.258288 | 0.249863 | intron-variant | MNAT1 | GRCh38.p7 | 14:60906572 | aatttttgatggatt[C/G]gttaaggggggtatg | 4331 |
rs2351538 | snp | A/G | 0.261608 | 0.24973 | intron-variant | MNAT1 | GRCh38.p7 | 14:60906610 | gaagattacttccaa[A/G]gtttttatctgagca | 4331 |
rs2882684 | snp | A/G | 0.495174 | 0.0488838 | intron-variant | MNAT1 | GRCh38.p7 | 14:60949744 | TTCATTTTTGGTACC[A/G]TTGATTGCATTAGCA | 4331 |
rs2882685 | snp | A/C | 0.02016 | 0.0983543 | intron-variant | MNAT1 | GRCh38.p7 | 14:60966345 | ggctggtctgaaact[A/C]ctgtcctcaggtgat | 4331 |
rs2882703 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | MNAT1 | GRCh38.p7 | 14:60924978 | TCCCAGTAAGTAAAT[A/G]TGTTACATTGTTAAT | 4331 |
rs3049888 | in-del | -/TT/TTTT/TTTTT | 0 | 0 | intron-variant | MNAT1 | GRCh38.p7 | 14:60741680 | TTTTTTTTTTTTTTT[-/TT/TTTT/TTTTT]AATTTTTAGTAGAGA | 4331 |
rs3049925 | in-del | -/TG | 0.128419 | 0.218444 | intron-variant | MNAT1 | GRCh38.p7 | 14:60861575 | ttttaaaaaaatttG[-/TG]AAAAGGTCTACAGGC | 4331 |
rs3080602 | in-del | -/A/AA | 0 | 0 | intron-variant | MNAT1 | GRCh38.p7 | 14:60942032 | aaaaaaaaaaaaaaa[-/A/AA]GTCAATAAATGAAAG | 4331 |
rs3081651 | in-del | -/TTT/TTTTTTTTTTT | 0 | 0 | intron-variant | MNAT1 | GRCh38.p7 | 14:60904978 | GTTCAGCAGttcctt[-/TTT/TTTTTTTTTTT]ttttttttttttttt | 4331 |
rs3783817 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | MNAT1 | GRCh38.p7 | 14:60963903 | TCCTGTCCAGTCATA[A/G]TATGTTTGTGACAAT | 4331 |
rs3783818 | snp | A/G | 0.309894 | 0.242719 | intron-variant | MNAT1 | GRCh38.p7 | 14:60915638 | GCTATTAATAAAACT[A/G]CCAGGAAGTAACACC | 4331 |
rs3783819 | snp | C/T | 0.469346 | 0.119947 | intron-variant | MNAT1 | GRCh38.p7 | 14:60849546 | ATCTTATTAGTATAA[C/T]AACAGACATATTAGA | 4331 |
rs3831810 | in-del | -/A | 0.229429 | 0.249152 | intron-variant | MNAT1 | GRCh38.p7 | 14:60805216 | CTTTTAAAAAAAAAG[-/A]AAAAAAGAAAAAACT | 4331 |
rs4151146 | snp | A/G | 0.0111728 | 0.0739025 | upstream-variant-2KB | MNAT1 | GRCh38.p7 | 14:60733262 | AACAAACAAACAAAC[A/G]CACAAAAATTGTCCT | 4331 |
rs4151147 | snp | A/T | 0.00438332 | 0.0466095 | upstream-variant-2KB | MNAT1 | GRCh38.p7 | 14:60733350 | AAATTTTATTTGCAC[A/T]TATGACATATTCATT | 4331 |
rs4151148 | snp | C/T | 0.0260105 | 0.111035 | upstream-variant-2KB | MNAT1 | GRCh38.p7 | 14:60733673 | AAAGAGATGATATGG[C/T]TTATTTATTAGATGA | 4331 |
rs4151149 | snp | A/G | 0.0023933 | 0.0345097 | upstream-variant-2KB | MNAT1 | GRCh38.p7 | 14:60734645 | GTATTAAGTTGCTTT[A/G]TGGAAGGCTAAGACC | 4331 |
rs4151150 | snp | C/T | 0.0387092 | 0.133627 | synonymous-codon, utr-variant-5-prime | MNAT1 | GRCh38.p7 | 14:60734916 | ATATCGGAACCCCTC[C/T]TTGAAGCTGATGGTG | 4331 |
rs4151151 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | MNAT1 | GRCh38.p7 | 14:60735116 | AAATAGACTGTAGCC[A/G]CTAGCCCCGAGCGGC | 4331 |
rs4151152 | snp | A/G | 0.0118339 | 0.076006 | intron-variant | MNAT1 | GRCh38.p7 | 14:60735306 | TATTTCATATGAAAT[A/G]TTTTTATTGAAAAAG | 4331 |
rs4151153 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | MNAT1 | GRCh38.p7 | 14:60735402 | TAATTAAAAAACCCT[A/G]TGTGTATGCCCACTT | 4331 |
rs4151154 | snp | C/G | 0.0240643 | 0.107019 | intron-variant | MNAT1 | GRCh38.p7 | 14:60735432 | TGTCCTGATGGAGTT[C/G]GGTTAGACTCCCATC | 4331 |
rs4151155 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | MNAT1 | GRCh38.p7 | 14:60735466 | AAAATGAAGAAAACC[C/T]GGACTGTAGGTAGTT | 4331 |
rs4151156 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | MNAT1 | GRCh38.p7 | 14:60735509 | ATAATAATGGCTGGC[A/G]TTTGAGTGCACATTT | 4331 |
rs4151157 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | MNAT1 | GRCh38.p7 | 14:60735612 | GATACTGGTATTTCC[A/G]TTTCACAGGGAAGGA | 4331 |
rs4151158 | snp | A/G | 0.0116955 | 0.0755709 | intron-variant | MNAT1 | GRCh38.p7 | 14:60739944 | GGATCACCTGAGGTC[A/G]GGAGTTCGAGACCAT | 4331 |
rs4151159 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MNAT1 | GRCh38.p7 | 14:60739982 | AACATAGTGAAACCC[C/T]GTCTCTACTAAAAAT | 4331 |
rs4151160 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | MNAT1 | GRCh38.p7 | 14:60745090 | GCATTCTGATCTCTG[C/T]CTATTTGGCTTAGCA | 4331 |
rs4151161 | snp | A/G | 0.0414363 | 0.137845 | intron-variant | MNAT1 | GRCh38.p7 | 14:60745480 | GGAATGCAGTGGTGC[A/G]ATCTTGGCTCATTGC | 4331 |
rs4151162 | snp | C/T | 0.0452528 | 0.143452 | intron-variant | MNAT1 | GRCh38.p7 | 14:60757428 | ACAGGCTAGAATGTT[C/T]GACATTTTCTGGTCA | 4331 |
rs4151163 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | MNAT1 | GRCh38.p7 | 14:60763457 | ATTTTATAGATGAAT[A/G]AAATAGGGTACAGAG | 4331 |
rs4151164 | snp | A/C | 0.00336134 | 0.0408579 | intron-variant | MNAT1 | GRCh38.p7 | 14:60763558 | AGGTTAGAGACCTTA[A/C]TGTTCTTTCAGTTCA | 4331 |
rs4151165 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | MNAT1 | GRCh38.p7 | 14:60763585 | TTCAATTTTCACTCG[A/G]TTAAATCCCAGTTTA | 4331 |
rs4151166 | snp | C/G/T | 0.00667218 | 0.0574451 | intron-variant | MNAT1 | GRCh38.p7 | 14:60768802 | TTCAGCTAGGCCTCA[C/G/T]TGATGACAAACCTTT | 4331 |
rs4151167 | snp | A/G | 0.282369 | 0.247896 | intron-variant | MNAT1 | GRCh38.p7 | 14:60769245 | ATTCTATATAAGTGT[A/G]TACATTATATATTTG | 4331 |
rs4151168 | snp | C/T | 0.321769 | 0.239477 | intron-variant | MNAT1 | GRCh38.p7 | 14:60769290 | ATATATTTTAAAAAA[C/T]TTGAAACAGGATCTT | 4331 |
rs4151169 | in-del | -/TACC | 0.314787 | 0.241459 | intron-variant | MNAT1 | GRCh38.p7 | 14:60769321 | CTGTTACCCAGGGTA[-/TACC]GAGTGCAGTGGGACA | 4331 |
rs4151170 | in-del | -/T | 0.015999 | 0.0879972 | intron-variant | MNAT1 | GRCh38.p7 | 14:60769344 | GTGGGACAACATAAC[-/T]TCACTGCAACTTTGT | 4331 |
rs4151171 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | MNAT1 | GRCh38.p7 | 14:60769526 | TGGGCTCAAGTGAGC[C/G]TTCTGCTTTGACCTC | 4331 |
rs4151172 | snp | G/T | 0.459004 | 0.137176 | intron-variant | MNAT1 | GRCh38.p7 | 14:60769932 | ggcctcccaaagcac[G/T]ggggttataggagtg | 4331 |
rs4151173 | snp | C/T | 0.0114282 | 0.0747228 | intron-variant | MNAT1 | GRCh38.p7 | 14:60769953 | TATAGGAGTGAGGCA[C/T]CATTCCTGGCCACCA | 4331 |
rs4151174 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | MNAT1 | GRCh38.p7 | 14:60770056 | ACTTTTTCATCTTGT[A/G]AAACTGAAATTCTAT | 4331 |
rs4151175 | snp | C/T | 0.0110494 | 0.0735024 | intron-variant | MNAT1 | GRCh38.p7 | 14:60774125 | AGATCTTTTAAAAGA[C/T]AGATCAATTTCTAAC | 4331 |
rs4151176 | snp | A/G | 0.203339 | 0.249931 | intron-variant | MNAT1 | GRCh38.p7 | 14:60774393 | ATAGGAATGAAGCTG[A/G]AGAGTTAGGTAGGGG | 4331 |
rs4151177 | snp | A/G | 0.238749 | 0.249747 | intron-variant | MNAT1 | GRCh38.p7 | 14:60774430 | CATGTAGTATCTTCA[A/G]TGGTGTGGTAAGTCA | 4331 |
rs4151178 | snp | C/T | 0.494358 | 0.0528145 | intron-variant | MNAT1 | GRCh38.p7 | 14:60774529 | ttcattttaaagata[C/T]gattttggctgttct | 4331 |
rs4151179 | snp | G/T | 0.0422008 | 0.138995 | intron-variant | MNAT1 | GRCh38.p7 | 14:60774640 | tagcagtacttcaag[G/T]aataagtgatagtgg | 4331 |
rs4151180 | snp | C/G | 0.0260105 | 0.111035 | intron-variant | MNAT1 | GRCh38.p7 | 14:60774743 | GTATTAATTAGATGT[C/G]GGTAATTAGGAAGTG | 4331 |
rs4151181 | snp | C/T | 0.0652144 | 0.168387 | intron-variant | MNAT1 | GRCh38.p7 | 14:60774897 | GCTTTGGACTTGTTA[C/T]GTTTTGTCATTGTTT | 4331 |
rs4151182 | snp | A/C | 0.451895 | 0.148806 | intron-variant | MNAT1 | GRCh38.p7 | 14:60775032 | catttacagctgttt[A/C]gactggatatgatca | 4331 |
rs4151183 | snp | A/G | 0.265453 | 0.249522 | intron-variant | MNAT1 | GRCh38.p7 | 14:60775118 | GTGGTTTACAGAGGA[A/G]AAGCAGCCAGAAAAA | 4331 |
rs4151184 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | MNAT1 | GRCh38.p7 | 14:60775310 | GGCTTTGGCAAGATT[A/G]AGGATATTGGTAAAA | 4331 |
rs4151185 | snp | A/G | 0.230017 | 0.2492 | intron-variant | MNAT1 | GRCh38.p7 | 14:60780471 | ATTTGGTTGTACCTG[A/G]AAAATGGGAAGAGTC | 4331 |
rs4151186 | snp | C/T | 0.0558544 | 0.157504 | intron-variant | MNAT1 | GRCh38.p7 | 14:60780583 | GGCCTACAAAATTCC[C/T]GTCAATGACTGAAGA | 4331 |
rs4151187 | snp | A/G | 0.0349115 | 0.127424 | intron-variant | MNAT1 | GRCh38.p7 | 14:60780637 | GTAATTTTGAAATGT[A/G]GTTTTCCTGAAATCA | 4331 |
rs4151188 | snp | C/T | 0.0479149 | 0.147179 | intron-variant | MNAT1 | GRCh38.p7 | 14:60780775 | ACCTATTTGACTCAC[C/T]ATGGAGTTAACATCA | 4331 |
rs4151189 | snp | C/G | 0.0260105 | 0.111035 | intron-variant | MNAT1 | GRCh38.p7 | 14:60785790 | CTTTGCATTTGACAA[C/G]GCACCTGGCATAGTA | 4331 |
rs4151190 | snp | A/G | 0.458545 | 0.137872 | intron-variant | MNAT1 | GRCh38.p7 | 14:60786235 | CATTTCTAATCAAGA[A/G]AAAGAGGTAGAAAAA | 4331 |
rs4151191 | in-del | -/ACTC | 0.141246 | 0.225106 | intron-variant | MNAT1 | GRCh38.p7 | 14:60786314 | TTAAAAAATATTTTA[-/ACTC]GTACTAATAAATGAG | 4331 |
rs4151192 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | MNAT1 | GRCh38.p7 | 14:60786426 | ATCTTTTATTGGTCA[C/T]ATGTAACAGTGGTTC | 4331 |
rs4151193 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | MNAT1 | GRCh38.p7 | 14:60786643 | ATGAAACATAACTAT[A/G]TTTTCCAAAACAAAA | 4331 |
rs4151194 | snp | A/G | 0.0448719 | 0.142907 | intron-variant, upstream-variant-2KB | MNAT1 | GRCh38.p7 | 14:60789984 | CCATAGTATATGAAT[A/G]TTTATGCACAAAGTT | 4331 |
rs4151195 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant, upstream-variant-2KB | MNAT1 | GRCh38.p7 | 14:60790378 | ATTGCTTCCTCTGCC[C/T]TATTGTTTATGTAAA | 4331 |
rs4151196 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant, upstream-variant-2KB | MNAT1 | GRCh38.p7 | 14:60790556 | TACATCTTACACATA[C/T]TGATTATTAATATAA | 4331 |
rs4151197 | snp | A/T | 0.0205511 | 0.0992634 | intron-variant, upstream-variant-2KB | MNAT1 | GRCh38.p7 | 14:60790728 | AGAAATATGGGATTC[A/T]CAGGGTAATGGTGAA | 4331 |
rs4151198 | snp | A/T | 0.0279526 | 0.114869 | intron-variant, upstream-variant-2KB | MNAT1 | GRCh38.p7 | 14:60790824 | GTAGTAAGGAAAATA[A/T]TATCTACATCATATC | 4331 |
rs4151199 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | MNAT1 | GRCh38.p7 | 14:60791332 | TTCTGAAAGTCTACT[A/G]TCTCTTCATAATGTT | 4331 |
rs4151200 | snp | C/T | 0.0279526 | 0.114869 | intron-variant | MNAT1 | GRCh38.p7 | 14:60795665 | TCACACATACTGGAG[C/T]GCTCAAAGTTCTTTA | 4331 |
rs4151201 | snp | C/T | 0.330016 | 0.236849 | intron-variant | MNAT1 | GRCh38.p7 | 14:60795722 | GCTAGCACCTCTTTC[C/T]TGTAATTGTCATTTG | 4331 |
rs4151202 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | MNAT1 | GRCh38.p7 | 14:60796846 | GTGTTGCTGTGGTCA[A/G]TGATGTCAGGTGTGG | 4331 |
rs4151203 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | MNAT1 | GRCh38.p7 | 14:60796938 | TAGTTTATTTTGGTA[A/T]GTGTATTTTTGTGTA | 4331 |
rs4151204 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | MNAT1 | GRCh38.p7 | 14:60796980 | ACACATGGGCATAGT[A/G]TATATATGTGTGTAT | 4331 |
rs4151205 | snp | G/T | 0.00337267 | 0.0409263 | intron-variant | MNAT1 | GRCh38.p7 | 14:60797067 | CTTTACTCTTTACTC[G/T]TTGTTAATAGTTTTG | 4331 |
rs4151206 | snp | C/T | 0.0418186 | 0.138422 | intron-variant, upstream-variant-2KB | MNAT1 | GRCh38.p7 | 14:60797929 | AGCAAGACTCCATCT[C/T]AAAAAATAAAAATAA | 4331 |
rs4151207 | snp | A/G | 0.0129027 | 0.0792771 | intron-variant | MNAT1 | GRCh38.p7 | 14:60803565 | CTTTCTGAGTCTAGA[A/G]CATGGAGTTCTATGG | 4331 |
rs4151208 | snp | A/G | 0.316485 | 0.240998 | intron-variant | MNAT1 | GRCh38.p7 | 14:60803592 | ATGGAATTATTAGAG[A/G]TGAGAGAAAAAAAGT | 4331 |
rs4151209 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | MNAT1 | GRCh38.p7 | 14:60803678 | TAGAAGGGTGCTGTT[A/G]AAGATAAACGTTTAA | 4331 |
rs4151210 | in-del | -/TAT | 0.0219753 | 0.102493 | intron-variant | MNAT1 | GRCh38.p7 | 14:60803833 | TAAAAATGAAAACAT[-/TAT]AATTTTAATAATAGC | 4331 |
rs4151211 | in-del | -/TT | 0.0229854 | 0.104711 | intron-variant | MNAT1 | GRCh38.p7 | 14:60803920 | TAACAATAGACTCTT[-/TT]CTGTGGTTATGACAA | 4331 |
rs4151212 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | MNAT1 | GRCh38.p7 | 14:60804002 | TTTATTCTTAGTTTC[A/G]TAATGAACAGATTAT | 4331 |
rs4151213 | in-del | -/G | 0.0111728 | 0.0739025 | intron-variant | MNAT1 | GRCh38.p7 | 14:60804244 | TAAACAGATAAAGGG[-/G]TCAAATGATTGTTAT | 4331 |
rs4151215 | snp | C/T | 0.0543475 | 0.155628 | intron-variant | MNAT1 | GRCh38.p7 | 14:60804646 | TCCTCCTGCCTCTAC[C/T]TCCCAAGTAGCTAGG | 4331 |
rs4151216 | in-del | -/A | 0.00358779 | 0.0422022 | intron-variant | MNAT1 | GRCh38.p7 | 14:60807672 | TTGAGTTGGAATTAT[-/A]AAAAGAGAGTTGTAA | 4331 |
rs4151218 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | MNAT1 | GRCh38.p7 | 14:60807792 | TATTTTTCTTCTTAA[A/G]TTCCAACTCCTTTAT | 4331 |
rs4151219 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | MNAT1 | GRCh38.p7 | 14:60807896 | AATGGGGATAAAACC[C/T]GTTTTTTGTTTGATA | 4331 |
rs4151220 | snp | A/T | 0.0422008 | 0.138995 | intron-variant | MNAT1 | GRCh38.p7 | 14:60807950 | TTTAACTCTTTTTTT[A/T]AAATTCTGATTCTTG | 4331 |
rs4151221 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MNAT1 | GRCh38.p7 | 14:60808252 | ATGAGTCACTGTGGT[A/G]TTTGTTTTTTATTGT | 4331 |
rs4151222 | snp | A/T | 0.0458763 | 0.144338 | intron-variant | MNAT1 | GRCh38.p7 | 14:60808825 | GACGGTGATGGAGCT[A/T]CCAAGAGGGAGATAA | 4331 |
rs4151223 | snp | G/T | 0.282895 | 0.247826 | intron-variant | MNAT1 | GRCh38.p7 | 14:60808948 | TAGTTACCTTTTTTG[G/T]TTTACCGAAAGAGTA | 4331 |
rs4151224 | snp | A/C | 0.0441095 | 0.141807 | intron-variant | MNAT1 | GRCh38.p7 | 14:60817685 | AAAGAAAATTAAAAT[A/C]TGTATGTTTGCTTTG | 4331 |
rs4151225 | snp | C/T | 0.0329836 | 0.124112 | intron-variant | MNAT1 | GRCh38.p7 | 14:60817785 | AGCCTCTTTGAACAA[C/T]ATGTTTTAGCACATT | 4331 |
rs4151226 | snp | A/G | 0.196149 | 0.244131 | intron-variant | MNAT1 | GRCh38.p7 | 14:60818143 | ATTAAAATGTGTCTG[A/G]GTGCTTATAATTAAT | 4331 |
rs4151227 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | MNAT1 | GRCh38.p7 | 14:60818623 | AATATTTAGTTTGAC[A/G]TGAAATGCTTATGGA | 4331 |
rs4151228 | snp | A/G | 0.00487149 | 0.0491123 | intron-variant | MNAT1 | GRCh38.p7 | 14:60818898 | TTTTTCAAGGATTAT[A/G]CTTTATAATTTTACA | 4331 |
rs4151229 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MNAT1 | GRCh38.p7 | 14:60818914 | CTTTATAATTTTACA[C/T]GATTTCTATAGTAAA | 4331 |
rs4151230 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | MNAT1 | GRCh38.p7 | 14:60818993 | TCTGGAAATATGGAT[A/G]GGTGCAGTATGAGGA | 4331 |
rs4151231 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | MNAT1 | GRCh38.p7 | 14:60819083 | TGTATGACTTTCTTA[A/C]TCTACTTACATTTTT | 4331 |
rs4151232 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | MNAT1 | GRCh38.p7 | 14:60819463 | ATTTAGATGTTTGAG[A/G]TGTAGCCACTCTAAA | 4331 |
rs4151233 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | MNAT1 | GRCh38.p7 | 14:60819580 | GTGATGGATATCTCA[A/G]TTACCCTGTTTTGGT | 4331 |
rs4151234 | snp | A/G | 0.00336134 | 0.0408579 | intron-variant | MNAT1 | GRCh38.p7 | 14:60824821 | TGTTTGTTATTTTTC[A/G]TAGTTAGATATATAA | 4331 |
rs4151235 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | MNAT1 | GRCh38.p7 | 14:60824840 | TTAGATATATAAATG[A/C]ATTATTTTATAATGC | 4331 |
rs4151236 | in-del | -/ATAAAAACA | 0.426035 | 0.177515 | intron-variant | MNAT1 | GRCh38.p7 | 14:60824997 | TAGAAAAGTAAAACA[-/ATAAAAACA]TCCTTAAGAGAGTGG | 4331 |
rs4151237 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | MNAT1 | GRCh38.p7 | 14:60825198 | GAAAGAATATGTAGA[C/T]TAAAATCACAACACA | 4331 |
rs4151238 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | MNAT1 | GRCh38.p7 | 14:60825362 | ACACAGAATACAGAT[A/G]AAAGTCTAAATGTTT | 4331 |
rs4151239 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | MNAT1 | GRCh38.p7 | 14:60829427 | AAATATTTAGTGTCA[A/G]TAGTTGGGAAAATTC | 4331 |
rs4151240 | snp | A/G | 0.328382 | 0.237395 | intron-variant | MNAT1 | GRCh38.p7 | 14:60829515 | AAAGGAAAAATTGTT[A/G]ATAGTCAAACTGTTG | 4331 |
rs4151241 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | MNAT1 | GRCh38.p7 | 14:60829678 | TAAAATCAGTATTCT[A/G]TGAGTGGTGGGAAGC | 4331 |
rs4151242 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | MNAT1 | GRCh38.p7 | 14:60837156 | TTCTTAGCTTGCTGG[A/G]CTCCGTGGGGGTGGG | 4331 |
rs4151243 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | MNAT1 | GRCh38.p7 | 14:60837268 | AGGCACCACTGGGTT[A/G]TGAAAAAAGAAACTG | 4331 |
rs4151244 | snp | A/G | 0.310632 | 0.242536 | intron-variant | MNAT1 | GRCh38.p7 | 14:60837627 | CCGCCTTCTGCATTG[A/G]TCTTGCTGCAAGCTG | 4331 |
rs4151245 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | MNAT1 | GRCh38.p7 | 14:60838218 | ACTGCTCAATGCAGG[C/T]TCTACTTCCTGGGCT | 4331 |
rs4151246 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | MNAT1 | GRCh38.p7 | 14:60838244 | GGGCTCAAGCAGTTA[C/T]CCTGCCTCAGCCTCC | 4331 |
rs4151247 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | MNAT1 | GRCh38.p7 | 14:60838500 | ATTATTTCTTTTCTT[C/T]TCTTTAATTAAGATT | 4331 |
rs4151248 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | MNAT1 | GRCh38.p7 | 14:60838578 | AGCAGTCACTGCAAA[A/G]ACACCAGCTGCAGTG | 4331 |
rs4151249 | snp | A/G | 0.0122695 | 0.0773576 | intron-variant | MNAT1 | GRCh38.p7 | 14:60849592 | CATTTTATAGTATTC[A/G]GTGAACTTGCATGTA | 4331 |
rs4151250 | snp | C/T | 0.0275645 | 0.114116 | intron-variant | MNAT1 | GRCh38.p7 | 14:60849919 | TCAGCTCACTGCAAC[C/T]TCCCCATCTCACGTT | 4331 |
rs4151251 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | MNAT1 | GRCh38.p7 | 14:60850078 | CTGACCTCAGGTGAT[A/G]CACCTGCCTCAGCCT | 4331 |
rs4151252 | snp | C/T | 0.191461 | 0.24305 | intron-variant | MNAT1 | GRCh38.p7 | 14:60850237 | TAGAAATTAGATCCA[C/T]AAATGTAATTACTTC | 4331 |
rs4151253 | snp | A/T | 0.0130921 | 0.0798413 | intron-variant | MNAT1 | GRCh38.p7 | 14:60850324 | TTACCCATTCTAGCA[A/T]AGTTTCACTGTTTTA | 4331 |
rs4151254 | snp | A/G | 0.127944 | 0.218179 | intron-variant | MNAT1 | GRCh38.p7 | 14:60850596 | GCTTTTGGGACTTGG[A/G]CAAATAACCTTATTC | 4331 |
rs4151255 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MNAT1 | GRCh38.p7 | 14:60851078 | TTTATGGGAATTTCT[A/G]TTAAGCAGATTATCA | 4331 |
rs4151256 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | MNAT1 | GRCh38.p7 | 14:60851113 | GTGAATACATGAAAA[A/G]ACAAACATTGGTCTG | 4331 |
rs4151257 | snp | C/T | 0.030278 | 0.119257 | intron-variant | MNAT1 | GRCh38.p7 | 14:60851387 | GCTCTGCAGATACTG[C/T]GTTTTTAAACAAATT | 4331 |
rs4151258 | snp | C/T | 0.190833 | 0.242898 | intron-variant | MNAT1 | GRCh38.p7 | 14:60851418 | GAAGGTTTCTGGCAA[C/T]CCTGTATGGGGCAAG | 4331 |
rs4151259 | in-del | -/C | 0.0166325 | 0.0896639 | intron-variant | MNAT1 | GRCh38.p7 | 14:60851442 | GGGCAAGTTTATCAG[-/C]CACCATTTTTCCAAC | 4331 |
rs4151260 | snp | A/G | 0.0418186 | 0.138422 | intron-variant | MNAT1 | GRCh38.p7 | 14:60851536 | TAAATTATTATTATT[A/G]ATATTTTTATTTTAC | 4331 |
rs4151261 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | MNAT1 | GRCh38.p7 | 14:60851551 | AATATTTTTATTTTA[C/T]TTTAAGTTCCGGCAT | 4331 |
rs4151265 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | MNAT1 | GRCh38.p7 | 14:60855961 | TCTCCTCAGGCCTCC[C/G]TATTCCTTTAGACAC | 4331 |
rs4151266 | in-del | -/TC | 0.0110494 | 0.0735024 | intron-variant | MNAT1 | GRCh38.p7 | 14:60856375 | TGTAATCCCTAACTC[-/TC]TTCAGTCCTATGAAG | 4331 |
rs4151267 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | MNAT1 | GRCh38.p7 | 14:60856431 | GGAGAAAAGTCTGAA[C/G]CTAGCAGAAGTTAAT | 4331 |
rs4151269 | snp | C/T | 0.0110494 | 0.0735024 | intron-variant | MNAT1 | GRCh38.p7 | 14:60856681 | AAGCCAGTGCTCATT[C/T]GCTTTTTTTTTTTTT | 4331 |
rs4151270 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MNAT1 | GRCh38.p7 | 14:60856743 | TGGAGTGCAGTGGCA[C/T]GATCTCAGCTCGTGG | 4331 |
rs4151271 | snp | C/T | 0.0887219 | 0.191022 | intron-variant | MNAT1 | GRCh38.p7 | 14:60856825 | AGCTGGGACTACAGG[C/T]GCTCACCACCACGCC | 4331 |
rs4151272 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | MNAT1 | GRCh38.p7 | 14:60856925 | ACCTCGTGATCCGCC[C/T]GCCTCGGCCTCCCAA | 4331 |
rs4151273 | snp | C/T | 0.039522 | 0.134904 | intron-variant | MNAT1 | GRCh38.p7 | 14:60856930 | GTGATCCGCCCGCCT[C/T]GGCCTCCCAAAGTGC | 4331 |
rs4151274 | snp | A/G | 0.122064 | 0.214785 | intron-variant | MNAT1 | GRCh38.p7 | 14:60861569 | ATTATTTTTTTAAAA[A/G]AATTTGTGAAAAGGT | 4331 |
rs4151275 | snp | A/G | 0.00345422 | 0.0414147 | intron-variant | MNAT1 | GRCh38.p7 | 14:60861715 | TTAGCTGATAAGCTA[A/G]TTTGAACCTGACTTT | 4331 |
rs4151276 | snp | G/T | 0.0111196 | 0.0737302 | intron-variant | MNAT1 | GRCh38.p7 | 14:60861962 | GAGTCCAGTTCAAAG[G/T]TGTTAGAATGAGAAG | 4331 |
rs4151277 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | MNAT1 | GRCh38.p7 | 14:60869711 | AAACCATATACTGAT[A/T]GGTATAGAACTGGAT | 4331 |
rs4151278 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | MNAT1 | GRCh38.p7 | 14:60869886 | CTATTTTAACATAGT[A/G]TGTGTTTAGAGTTAA | 4331 |
rs4151279 | snp | A/C | 0.0433465 | 0.140692 | intron-variant | MNAT1 | GRCh38.p7 | 14:60869987 | GACAAATCTTAGTAA[A/C]TTATAAACAATTTTT | 4331 |
rs4151280 | snp | A/G | 0.00351493 | 0.0417745 | intron-variant | MNAT1 | GRCh38.p7 | 14:60870401 | ACATTTTTACTTTTA[A/G]AGCCTTATTTCTTTA | 4331 |
rs4151281 | snp | A/G | 0.277067 | 0.24853 | intron-variant | MNAT1 | GRCh38.p7 | 14:60870427 | CTTTATCAATTATAT[A/G]ACAACAGTAACAAAA | 4331 |
rs4151282 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | MNAT1 | GRCh38.p7 | 14:60870468 | CTTTAGTTTTGTGCC[A/G]TACTTTTCAAAGTCA | 4331 |
rs4151283 | snp | G/T | 0.00350262 | 0.0417018 | intron-variant | MNAT1 | GRCh38.p7 | 14:60870629 | TTTCTTTTGAGTTTA[G/T]TTTATATTTCTAGCT | 4331 |
rs4151284 | snp | A/G | 0.00345422 | 0.0414147 | intron-variant | MNAT1 | GRCh38.p7 | 14:60870664 | TTACTGAACATTTCT[A/G]CTTGGATATTTTATA | 4331 |
rs4151285 | snp | A/T | 0.0588605 | 0.161139 | intron-variant | MNAT1 | GRCh38.p7 | 14:60870717 | AAACCACCATCTTAA[A/T]CTCTTTATTTTTAAT | 4331 |
rs4151286 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | MNAT1 | GRCh38.p7 | 14:60870744 | TAATAGCTTTATCAA[A/G]ATATAATTTACTTAC | 4331 |
rs4151287 | snp | G/T | 0.0154538 | 0.0865337 | intron-variant | MNAT1 | GRCh38.p7 | 14:60870870 | TCATCACTCCAAAGA[G/T]GTCTCTGATACTCAT | 4331 |
rs4151288 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | MNAT1 | GRCh38.p7 | 14:60874057 | AAAATATGTGAAGAT[G/T]TTAAAGGTTTACTAA | 4331 |
rs4151289 | snp | C/G | 0.134802 | 0.221877 | intron-variant | MNAT1 | GRCh38.p7 | 14:60875930 | TCTGAAATGCACACG[C/G]AGTGTTGGTGAGACT | 4331 |
rs4151290 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | MNAT1 | GRCh38.p7 | 14:60875981 | GTCACAGTATTTTTC[C/G]TTTCCCTCACTTACC | 4331 |
rs4151291 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | MNAT1 | GRCh38.p7 | 14:60876599 | CCATGTTCCTAGTCT[A/G]TGGTAACCACTGATC | 4331 |
rs4151292 | snp | C/T | 0.104859 | 0.203554 | intron-variant | MNAT1 | GRCh38.p7 | 14:60876609 | AGTCTATGGTAACCA[C/T]TGATCTACTTTCTGT | 4331 |
rs4151293 | snp | A/G | 0.00338409 | 0.040995 | intron-variant | MNAT1 | GRCh38.p7 | 14:60879237 | TTTGTTCTTTTTTCA[A/G]TTTAGTAGAATTCAC | 4331 |
rs4151294 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | MNAT1 | GRCh38.p7 | 14:60879431 | TTTGAAGTCTCTTGT[A/G]TTTGATGACTTCTAC | 4331 |
rs4151295 | snp | G/T | 0.00336134 | 0.0408579 | intron-variant | MNAT1 | GRCh38.p7 | 14:60879438 | TCTCTTGTATTTGAT[G/T]ACTTCTACCATGGAC | 4331 |
rs4151296 | snp | G/T | 0.00335007 | 0.0407899 | intron-variant | MNAT1 | GRCh38.p7 | 14:60879943 | TTATAGAACTTTACT[G/T]TTTTGTGAAAAATGA | 4331 |
rs4151297 | snp | A/G | 0.00333889 | 0.0407222 | intron-variant | MNAT1 | GRCh38.p7 | 14:60880100 | ATGGCGTTTATTTTC[A/G]GTCATGAGTGTTTTT | 4331 |
rs4151298 | snp | G/T | 0.00332778 | 0.0406548 | intron-variant | MNAT1 | GRCh38.p7 | 14:60880145 | AATTGGGGCTTAATT[G/T]AGTTAGTAGTAAGCC | 4331 |
rs4151299 | snp | A/G | 0.0112991 | 0.0743093 | intron-variant | MNAT1 | GRCh38.p7 | 14:60880664 | AATAATAAAACCTAC[A/G]TGCATCTTCAAAAAC | 4331 |
rs4151300 | snp | A/G | 0.382279 | 0.212137 | intron-variant | MNAT1 | GRCh38.p7 | 14:60880936 | GATAGACAATATTGC[A/G]TTTTATAATGTAAAA | 4331 |
rs4151302 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | MNAT1 | GRCh38.p7 | 14:60883759 | CAATTTTTTGCATCA[A/G]TATTTTATAGTTTTC | 4331 |
rs4151303 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | MNAT1 | GRCh38.p7 | 14:60883955 | TGTTTATCAGTTCTA[A/G]TAGTTTTTTTGTGAA | 4331 |
rs4151304 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | MNAT1 | GRCh38.p7 | 14:60884268 | TTTGAGGGTTTTTAC[C/T]ATGAAAGAATGTTGA | 4331 |
rs4151306 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | MNAT1 | GRCh38.p7 | 14:60891830 | tgctgtgtcccatac[A/G]ttttggtatggcttg | 4331 |
rs4151307 | snp | C/T | 0.0244538 | 0.107838 | intron-variant | MNAT1 | GRCh38.p7 | 14:60891872 | ATTCATTTCCAACTA[C/T]TTTCTAATTTTCCTT | 4331 |
rs4151309 | snp | C/G | 0.0252325 | 0.109451 | intron-variant | MNAT1 | GRCh38.p7 | 14:60892242 | atctattattgagag[C/G]ggagtattgaaggct | 4331 |
rs4151310 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | MNAT1 | GRCh38.p7 | 14:60892557 | ATGTATTCTACCAAT[C/T]TCTATCTTTTGATTG | 4331 |
rs4151311 | snp | A/C | 0.0193772 | 0.0965046 | intron-variant | MNAT1 | GRCh38.p7 | 14:60892814 | AGTTGTAGCACTCTG[A/C]ATTTATACAAGCTTA | 4331 |
rs4151312 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | MNAT1 | GRCh38.p7 | 14:60892846 | cttcagtaacatgca[A/G]aaactctgcttttaa | 4331 |
rs4151313 | snp | C/T | 0.0114282 | 0.0747228 | intron-variant | MNAT1 | GRCh38.p7 | 14:60892951 | TTAATAAATTATTTT[C/T]TTAAATGTGTTAGTT | 4331 |
rs4151314 | snp | A/G | 0.114738 | 0.210248 | intron-variant | MNAT1 | GRCh38.p7 | 14:60893042 | agactaattttttta[A/G]aaaagatattagtct | 4331 |
rs4151315 | snp | A/G | 0.0622301 | 0.165053 | intron-variant | MNAT1 | GRCh38.p7 | 14:60893071 | CTCTTAAATCTTACA[A/G]TGTTATACCTTTTGA | 4331 |
rs4151316 | snp | A/C | 0.492727 | 0.0598633 | intron-variant | MNAT1 | GRCh38.p7 | 14:60897101 | CTTAGAAGTTCATAT[A/C]ACATTTTAATGAATG | 4331 |
rs4151317 | snp | A/G | 0.197393 | 0.244402 | intron-variant | MNAT1 | GRCh38.p7 | 14:60898003 | gtctttctgtgtctg[A/G]tttattttacttaac | 4331 |
rs4151318 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | MNAT1 | GRCh38.p7 | 14:60898085 | CTTTGAATGGCTAAA[C/T]AGTAATACATTGTGT | 4331 |
rs4151319 | snp | A/T | 0.0111196 | 0.0737302 | intron-variant | MNAT1 | GRCh38.p7 | 14:60898431 | CAGCATGTGTAATTT[A/T]TTGTCTTTTTAATAA | 4331 |
rs4151320 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | MNAT1 | GRCh38.p7 | 14:60898452 | TTTTTAATAATAGCC[C/T]TGCTAACTGGGGTAA | 4331 |
rs4151322 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MNAT1 | GRCh38.p7 | 14:60899052 | TGGTATCATTGTTGA[C/T]TATTAATTGGCCGTA | 4331 |
rs4151323 | snp | C/T | 0.323197 | 0.239044 | intron-variant | MNAT1 | GRCh38.p7 | 14:60899072 | AATTGGCCGTAAACA[C/T]GTGGCTTTATTTCCG | 4331 |
rs4151324 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | MNAT1 | GRCh38.p7 | 14:60902919 | TATTAGGTAAATATC[G/T]GGGTTTTTATCTAGG | 4331 |
rs4151325 | snp | C/T | 0.0252325 | 0.109451 | intron-variant | MNAT1 | GRCh38.p7 | 14:60904003 | CAGCCTCCCGAGTAG[C/T]GGGGACTGCAGGCAC | 4331 |
rs4151326 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MNAT1 | GRCh38.p7 | 14:60904175 | TGTGCCCGACCTTAA[A/G]TTTATATGTTAGTTT | 4331 |
rs4151327 | snp | G/T | 0.0252325 | 0.109451 | intron-variant | MNAT1 | GRCh38.p7 | 14:60904207 | ACAGAAAGTCTTGGG[G/T]CATCAGAAAATCAAA | 4331 |
rs4151328 | snp | A/G | 0.0966517 | 0.197444 | intron-variant | MNAT1 | GRCh38.p7 | 14:60904556 | GCTTCTTTCATCAAC[A/G]GTCAGACACAGGGCA | 4331 |
rs4151329 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | MNAT1 | GRCh38.p7 | 14:60904750 | TCAGAAAGAAAGCAC[C/T]AAGTTAAAAAAAGTA | 4331 |
rs4151330 | snp | A/G | 0.39214 | 0.205661 | intron-variant | MNAT1 | GRCh38.p7 | 14:60904827 | AAAAAAGCAGATTCA[A/G]TTTATTATTGGACTT | 4331 |
rs4151331 | snp | C/G | 0.0244538 | 0.107838 | intron-variant | MNAT1 | GRCh38.p7 | 14:60905005 | TTTTGGACGGAGTCT[C/G]GCTCTGTTGCCCAGG | 4331 |
rs4151332 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | MNAT1 | GRCh38.p7 | 14:60905315 | TTAAAATTCAACTGT[A/T]ATAAAACCAACAATA | 4331 |
rs4151333 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | MNAT1 | GRCh38.p7 | 14:60905319 | AATTCAACTGTAATA[A/G]AACCAACAATAACAG | 4331 |
rs4151334 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | MNAT1 | GRCh38.p7 | 14:60905355 | TATTGAATATGTTAG[A/G]TGCTGTTAGATATTT | 4331 |
rs4151335 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | MNAT1 | GRCh38.p7 | 14:60905403 | TGTTAGATATAGCAG[A/C]TAAACCAGGGTTTTC | 4331 |
rs4151336 | snp | A/G | 0.0114282 | 0.0747228 | intron-variant | MNAT1 | GRCh38.p7 | 14:60905656 | CTTAGCGGGGGTGGA[A/G]GTGAAAGTCATGGAG | 4331 |
rs4151337 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | MNAT1 | GRCh38.p7 | 14:60905663 | GGGGTGGAGGTGAAA[A/G]TCATGGAGTATGAAG | 4331 |
rs4151338 | in-del | -/T | 0.0115603 | 0.0751433 | intron-variant | MNAT1 | GRCh38.p7 | 14:60905768 | TTCCTTCGTTTTTTT[-/T]GCTGTGTTCAGGCCC | 4331 |
rs4151339 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | MNAT1 | GRCh38.p7 | 14:60905882 | CTGGAAACACCTTCA[C/T]AGACGCACCCAGAAA | 4331 |
rs4151340 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | MNAT1 | GRCh38.p7 | 14:60906085 | TACCTGAATTAGCAA[A/G]GAAATGAGTCATTTG | 4331 |
rs4151341 | snp | C/T | 0.0360663 | 0.129354 | intron-variant | MNAT1 | GRCh38.p7 | 14:60906326 | TTACTTTGAAGGAGA[C/T]GCGAAGTCATAGGAG | 4331 |
rs4151342 | snp | G/T | 0.0452528 | 0.143452 | intron-variant | MNAT1 | GRCh38.p7 | 14:60906341 | tgcgaagtcatagga[G/T]aattttgaacagaag | 4331 |
rs4151343 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | MNAT1 | GRCh38.p7 | 14:60906346 | AGTCATAGGAGAATT[C/T]TGAACAGAAGTTGCC | 4331 |
rs4151344 | snp | A/G | 0.0252325 | 0.109451 | intron-variant | MNAT1 | GRCh38.p7 | 14:60906385 | ACTTTCATCTAGAAA[A/G]GTCTGTCATCAGAGA | 4331 |
rs4151347 | in-del | -/C | 0.0490535 | 0.14873 | intron-variant | MNAT1 | GRCh38.p7 | 14:60906967 | CACCTTTCCACCCCC[-/C]AACCCCAATAGCCAC | 4331 |
rs4151348 | snp | A/C/G | 0.00597247 | 0.0543191 | intron-variant | MNAT1 | GRCh38.p7 | 14:60906983 | CCCCCAACCCCAATA[A/C/G]CCACAAACTTAGCTA | 4331 |
rs4151349 | snp | A/G | 0.0310518 | 0.120672 | intron-variant | MNAT1 | GRCh38.p7 | 14:60914843 | TAGAATCAAATGGCT[A/G]TACTTTGGGAGAGCA | 4331 |
rs4151350 | snp | A/G | 0.0252325 | 0.109451 | intron-variant | MNAT1 | GRCh38.p7 | 14:60915412 | tttcagctgagccac[A/G]taTTTTAAACTTATT | 4331 |
rs4151351 | snp | A/G | 0.284733 | 0.247575 | intron-variant | MNAT1 | GRCh38.p7 | 14:60916029 | GGTATTTCTTGGAGC[A/G]CTGTGGTAACTTTTC | 4331 |
rs4151352 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | MNAT1 | GRCh38.p7 | 14:60922451 | ATGTTACCACAGAAA[C/T]CTGAAATTGATTTGG | 4331 |
rs4151353 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | MNAT1 | GRCh38.p7 | 14:60922762 | AAGTAAGATTTCTCC[A/T]TTGCCAAGGCCACAA | 4331 |
rs4151354 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | MNAT1 | GRCh38.p7 | 14:60926873 | TCCCCTTGTGAACCA[A/G]CCCCATCCTGAGGCC | 4331 |
rs4151355 | snp | C/T | 0.00332778 | 0.0406548 | intron-variant | MNAT1 | GRCh38.p7 | 14:60927068 | GCCAGGGACTGTGGG[C/T]AAAGACCAATATGTA | 4331 |
rs4151356 | snp | A/G | 0.0341408 | 0.126114 | intron-variant | MNAT1 | GRCh38.p7 | 14:60927131 | TTCAAAAGGAAAACT[A/G]TATCTTCTGACTTGA | 4331 |
rs4151357 | snp | G/T | 0.0174175 | 0.0916809 | intron-variant | MNAT1 | GRCh38.p7 | 14:60927140 | AAAACTATATCTTCT[G/T]ACTTGATGTGGGCCT | 4331 |
rs4151358 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | MNAT1 | GRCh38.p7 | 14:60927145 | TATATCTTCTGACTT[G/T]ATGTGGGCCTTCTTG | 4331 |
rs4151359 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | MNAT1 | GRCh38.p7 | 14:60927371 | TTTATTGAAGTAAAA[C/T]TTACATACCACAAAG | 4331 |
rs4151360 | snp | A/T | 0.0107246 | 0.0724382 | intron-variant | MNAT1 | GRCh38.p7 | 14:60927531 | AGGAGCCCTGAATTC[A/T]CAAGGGTGCCCTGTA | 4331 |
rs4151361 | snp | G/T | 0.0569829 | 0.158885 | intron-variant | MNAT1 | GRCh38.p7 | 14:60931688 | ATGTAAGACCCTTAA[G/T]ATTTTTGATTTAGTC | 4331 |
rs4151362 | snp | A/G | 0.20511 | 0.245937 | intron-variant | MNAT1 | GRCh38.p7 | 14:60931880 | AACAATGGTGAATTA[A/G]TTATATACTCCCTTA | 4331 |
rs4151363 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | MNAT1 | GRCh38.p7 | 14:60932172 | TTATCTTTTTTCTTA[C/T]GTAAGTTTAGTCTAA | 4331 |
rs4151364 | snp | A/G | 0.279195 | 0.248289 | intron-variant | MNAT1 | GRCh38.p7 | 14:60932511 | ATAGTTCAAGAAACT[A/G]TCTTACGTGGAGTGT | 4331 |
rs4151365 | snp | A/T | 0.0333695 | 0.124785 | intron-variant | MNAT1 | GRCh38.p7 | 14:60932579 | CTTTAAATGTTAGAT[A/T]GATTTTAGTTTACCA | 4331 |
rs4151366 | snp | A/T | 0.0107246 | 0.0724382 | intron-variant | MNAT1 | GRCh38.p7 | 14:60932607 | CCACTTTAGAAAACT[A/T]TTTTTAACTGTTTTT | 4331 |
rs4151367 | snp | C/T | 0.0256215 | 0.110247 | intron-variant | MNAT1 | GRCh38.p7 | 14:60932769 | TTATCATTTTTAAAG[C/T]TATGTGTTAGAGATC | 4331 |
rs4151368 | snp | C/T | 0.0379877 | 0.132479 | intron-variant | MNAT1 | GRCh38.p7 | 14:60932819 | TAAATATCAGTGTTT[C/T]TGCATCATAATTTGG | 4331 |
rs4151369 | snp | A/G | 0.0490535 | 0.14873 | intron-variant | MNAT1 | GRCh38.p7 | 14:60933132 | GTAATATATGGAAGA[A/G]CCTAGAATACTGACT | 4331 |
rs4151370 | snp | A/G | 0.0494327 | 0.149241 | intron-variant | MNAT1 | GRCh38.p7 | 14:60933221 | ACTGATTTTAGGTCT[A/G]TTGAGATTTTCTACC | 4331 |
rs4151371 | snp | A/C | 0.00337267 | 0.0409263 | intron-variant | MNAT1 | GRCh38.p7 | 14:60933487 | TTGTGCTCTTAACAC[A/C]AAGGGAAAGTCACAG | 4331 |
rs4151372 | snp | A/G | 0.00333889 | 0.0407222 | intron-variant | MNAT1 | GRCh38.p7 | 14:60933665 | AATCACATCTAAAAC[A/G]TGGATCTAGACAATC | 4331 |
rs4151373 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | MNAT1 | GRCh38.p7 | 14:60934124 | AAGTCCAAGTTGTTG[A/G]CAATTCATTCGTAGA | 4331 |
rs4151374 | snp | A/G | 0.477937 | 0.102688 | intron-variant | MNAT1 | GRCh38.p7 | 14:60935235 | GGGGCCATATTTCAG[A/G]CAATTGTCACCTTCC | 4331 |
rs4151375 | snp | A/C | 0.0107246 | 0.0724382 | intron-variant | MNAT1 | GRCh38.p7 | 14:60944515 | ATGAGAAATAGACTT[A/C]TATCGTTTAAGCCAC | 4331 |
rs4151376 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | MNAT1 | GRCh38.p7 | 14:60946867 | gaaatagacttctat[C/T]gtttaagccactgag | 4331 |
rs4151377 | snp | G/T | 0.0110494 | 0.0735024 | intron-variant | MNAT1 | GRCh38.p7 | 14:60944547 | GAGTGTGTGGTATTT[G/T]GTTATAGCAGTTGAA | 4331 |
rs4151378 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | MNAT1 | GRCh38.p7 | 14:60944576 | AAGTAGACAAATAGA[A/C]TATTACCATATAGCT | 4331 |
rs4151379 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | MNAT1 | GRCh38.p7 | 14:60944591 | CTATTACCATATAGC[G/T]TTAGAATCAAACATT | 4331 |
rs4151380 | snp | C/G | 0.144296 | 0.226554 | intron-variant | MNAT1 | GRCh38.p7 | 14:60944938 | ACTCTTTGCTCCAAG[C/G]AAATAAATATTTAGA | 4331 |
rs4151381 | snp | C/T | 0.144632 | 0.226711 | intron-variant | MNAT1 | GRCh38.p7 | 14:60944950 | AAGGAAATAAATATT[C/T]AGAAAACTCTTACTG | 4331 |
rs4151382 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MNAT1 | GRCh38.p7 | 14:60945651 | GTATTTTAGTGTTTT[C/T]GTTATATTGTGACAA | 4331 |
rs4151383 | snp | C/T | 0.140581 | 0.224783 | intron-variant | MNAT1 | GRCh38.p7 | 14:60945740 | TTAAATTAGTTCTGC[C/T]GAGAGAAGCTGGAGA | 4331 |
rs4151384 | snp | A/C | 0.0123036 | 0.0774623 | intron-variant | MNAT1 | GRCh38.p7 | 14:60945846 | CCCACAGTGGCTTTC[A/C]CACATCATCAGTTTC | 4331 |
rs4151385 | snp | A/G | 0.275197 | 0.248727 | intron-variant | MNAT1 | GRCh38.p7 | 14:60946170 | TCTCTGTGTTGAAAT[A/G]TTTCCTTTACAACAT | 4331 |
rs4151386 | snp | A/C | 0.275197 | 0.248727 | intron-variant | MNAT1 | GRCh38.p7 | 14:60946181 | AAATATTTCCTTTAC[A/C]ACATGAACATACTCA | 4331 |
rs4151387 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | MNAT1 | GRCh38.p7 | 14:60949974 | CTAGTCCTTTGACTT[A/G]GATATTTTATGAACC | 4331 |
rs4151388 | snp | A/T | 0.0118339 | 0.076006 | intron-variant | MNAT1 | GRCh38.p7 | 14:60949978 | TCCTTTGACTTAGAT[A/T]TTTTATGAACCAATT | 4331 |
rs4151389 | in-del | -/A | 0.0130713 | 0.0797797 | intron-variant | MNAT1 | GRCh38.p7 | 14:60950190 | AATACCTTAAAAAAT[-/A]TTTAGCTTTGAGTGT | 4331 |
rs4151390 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | MNAT1 | GRCh38.p7 | 14:60950594 | AACATTATGACTTTT[C/T]GTTTTGTTTTATTTT | 4331 |
rs4151391 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | MNAT1 | GRCh38.p7 | 14:60950750 | ACCCCTTTCATCTTT[C/T]GACGAAGCTTCATAA | 4331 |
rs4151392 | snp | A/G | 0.472896 | 0.113214 | intron-variant | MNAT1 | GRCh38.p7 | 14:60952413 | GAGAGAACATACTGT[A/G]AATAGGGAGATCAAT | 4331 |
rs4151393 | snp | A/G | 0.21725 | 0.247846 | intron-variant | MNAT1 | GRCh38.p7 | 14:60952744 | CAGATAAACATATTG[A/G]ACTATAATTAAGATA | 4331 |
rs4151394 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | MNAT1 | GRCh38.p7 | 14:60960984 | tttctttttttgaga[C/T]ggagtgttgctcttg | 4331 |
rs4151395 | snp | C/G | 0.0115144 | 0.0749975 | intron-variant | MNAT1 | GRCh38.p7 | 14:60961014 | GTTGCCCAGGCTGGA[C/G]TGCAATGGTGCGATC | 4331 |
rs4151396 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | MNAT1 | GRCh38.p7 | 14:60961072 | GGTTCAAGTGATTCT[C/T]CTGCCTCAGCCTCCC | 4331 |
rs4151397 | snp | A/T | 0.0505692 | 0.150756 | intron-variant | MNAT1 | GRCh38.p7 | 14:60961092 | CTCAGCCTCCCGAGT[A/T]GCTGAGATTACAGGC | 4331 |
rs4151398 | snp | C/T | 0.00339558 | 0.0410641 | intron-variant | MNAT1 | GRCh38.p7 | 14:60961399 | CCTGAGCTGAAACCA[C/T]CTGTCCCCTATATTC | 4331 |
rs4151399 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | MNAT1 | GRCh38.p7 | 14:60961475 | TCTCTCTGGATCACC[A/G]TTATACTCCCCTTGC | 4331 |
rs4151400 | snp | C/T | 0.296873 | 0.245566 | intron-variant | MNAT1 | GRCh38.p7 | 14:60961694 | GGCTTTGTTCTCTGT[C/T]TTATTATCAGGGCTA | 4331 |
rs4151401 | snp | A/G | 0.0116955 | 0.0755709 | intron-variant | MNAT1 | GRCh38.p7 | 14:60961703 | CTCTGTTTTATTATC[A/G]GGGCTACTTCAATAC | 4331 |
rs4151402 | snp | A/G | 0.0236746 | 0.106192 | intron-variant | MNAT1 | GRCh38.p7 | 14:60961848 | TTATAAAGATATGAT[A/G]AAAATTCTGGCACAT | 4331 |
rs4151403 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | MNAT1 | GRCh38.p7 | 14:60964253 | TTTCTAATGCTTAAT[C/T]GTATCTTACGCCCTT | 4331 |
rs4151404 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | MNAT1 | GRCh38.p7 | 14:60964487 | CTTTGAGTTTAGTCT[A/G]CTTTCAGTAAAAATA | 4331 |
rs4151405 | snp | G/T | 0.239902 | 0.249796 | intron-variant | MNAT1 | GRCh38.p7 | 14:60967503 | GCTAGATTGTCCAAT[G/T]TTTTTTAGGCCTGTT | 4331 |
rs4151406 | snp | C/T | 0.00335007 | 0.0407899 | intron-variant | MNAT1 | GRCh38.p7 | 14:60967533 | TTTGTCTATTTTTGT[C/T]AAGATATAAATGTTT | 4331 |
rs4151407 | snp | A/G | 0.0110494 | 0.0735024 | intron-variant | MNAT1 | GRCh38.p7 | 14:60967900 | GGAAGGAGAGCATTA[A/G]TTAGGTGTCCAAAAA | 4331 |
rs4151408 | snp | A/G | 0.236144 | 0.249616 | intron-variant | MNAT1 | GRCh38.p7 | 14:60968059 | GGCACTCCATGTACA[A/G]TTGGTATGTTTCCTT | 4331 |
rs4151409 | snp | C/T | 0.0763817 | 0.17988 | utr-variant-3-prime, splice-donor-variant, intron-variant | MNAT1 | GRCh38.p7 | 14:60968399 | GGGAGCTAGCAAAAG[C/T]AAAGCAGACTTATAA | 4331 |
rs4151410 | snp | A/G | 0.00335007 | 0.0407899 | utr-variant-3-prime | MNAT1 | GRCh38.p7 | 14:60968641 | GGTTGTGACAGACTT[A/G]TAAAATCTTTTTAAA | 4331 |
rs4151411 | snp | C/T | 0.00119737 | 0.0244387 | downstream-variant-500B, utr-variant-3-prime | MNAT1 | GRCh38.p7 | 14:60968714 | TATTACAGTGTTTTA[C/T]TTGAACACATTTTAA | 4331 |
rs4151412 | snp | C/T | 0.0107246 | 0.0724382 | downstream-variant-500B, utr-variant-3-prime | MNAT1 | GRCh38.p7 | 14:60968776 | TATCCAAGTCTATTA[C/T]TTCTTCTCATAAAAT | 4331 |
rs4151413 | snp | A/G | 0.0225045 | 0.103662 | downstream-variant-500B, utr-variant-3-prime | MNAT1 | GRCh38.p7 | 14:60968835 | TACTAGTCCAGACAA[A/G]TGGATATATTTCCTT | 4331 |
rs4151414 | snp | A/G | 0.0103295 | 0.0711199 | downstream-variant-500B, utr-variant-3-prime | MNAT1 | GRCh38.p7 | 14:60968959 | GCAAACCTTGATCAA[A/G]GTGTTATAGTTCCCA | 4331 |
rs4411433 | snp | C/G | 0 | 0 | intron-variant | MNAT1 | GRCh38.p7 | 14:60912286 | atccagtttgccagt[C/G]tgtgtcttttaattg | 4331 |
rs4412892 | snp | A/G | 0.28052 | 0.24813 | intron-variant | MNAT1 | GRCh38.p7 | 14:60947947 | TTGCTGCTATGTCAT[A/G]TAATTGGACAGTTAA | 4331 |
rs4480717 | snp | C/G | 0.0185938 | 0.0946107 | intron-variant | MNAT1 | GRCh38.p7 | 14:60826341 | tttttttttgagatg[C/G]agtctcactctgtcc | 4331 |
rs4583139 | snp | C/T | 0.450859 | 0.148847 | intron-variant | MNAT1 | GRCh38.p7 | 14:60889003 | aggaagaatcaatat[C/T]gtgaaaatggccata | 4331 |
rs4587888 | snp | A/G | 0.450859 | 0.148847 | intron-variant | MNAT1 | GRCh38.p7 | 14:60889004 | ggaagaatcaatatt[A/G]tgaaaatggccatac | 4331 |
rs4611379 | snp | C/T | 0.2768 | 0.248559 | intron-variant | MNAT1 | GRCh38.p7 | 14:60955530 | agctgggcgtggtgg[C/T]gggtgcctgtaatcc | 4331 |
rs4899017 | snp | C/T | 0 | 0 | intron-variant | MNAT1 | GRCh38.p7 | 14:60747618 | ggaagttgttctggg[C/T]gagtcagtaagtagt | 4331 |
rs4899018 | snp | C/T | 0.188946 | 0.24243 | intron-variant | MNAT1 | GRCh38.p7 | 14:60762946 | TTATCAGTTGTTGTA[C/T]AGAGATAGCTTATTA | 4331 |
rs4899019 | snp | G/T | 0.18989 | 0.242666 | intron-variant | MNAT1 | GRCh38.p7 | 14:60776592 | GGAGGAGCAGATACT[G/T]TTAGGGGAGGCCATA | 4331 |
rs4899020 | snp | A/G | 0.232651 | 0.249397 | intron-variant | MNAT1 | GRCh38.p7 | 14:60843887 | caagtcacaacgata[A/G]ttctcctgtttagaa | 4331 |
rs4899021 | snp | G/T | 0.411074 | 0.191194 | intron-variant | MNAT1 | GRCh38.p7 | 14:60855235 | tcaagccagtggttc[G/T]tagcttcctaggctc | 4331 |
rs4899022 | snp | C/T | 0.249886 | 0.25 | intron-variant | MNAT1 | GRCh38.p7 | 14:60858103 | ccagtaatgggattg[C/T]tgggtcaaatggtat | 4331 |
rs4899023 | snp | A/G | 0.246769 | 0.249979 | intron-variant | MNAT1 | GRCh38.p7 | 14:60858175 | acaatggttaaacta[A/G]tttacactcctacca | 4331 |
rs4899024 | snp | C/T | 0.197393 | 0.244402 | intron-variant | MNAT1 | GRCh38.p7 | 14:60893953 | TTCTTAGTGTTCCTA[C/T]TTCTTTCCCAGAGGC | 4331 |
rs4902001 | snp | C/T | 0.32885 | 0.23724 | intron-variant | MNAT1 | GRCh38.p7 | 14:60759709 | ACATGCCATACTATT[C/T]ATTGCAGGTATACTG | 4331 |
rs4902002 | snp | A/G | 0.447421 | 0.153379 | intron-variant | MNAT1 | GRCh38.p7 | 14:60762693 | TCTGGGCAACAGAGC[A/G]AGACTCTGTCTCAAA | 4331 |
rs4902005 | snp | A/G | 0.239614 | 0.249784 | intron-variant | MNAT1 | GRCh38.p7 | 14:60802497 | GGGCTTTGTAAACTG[A/G]GCTGTCAGTTAAGAT | 4331 |
rs4902006 | snp | C/G | 0.239614 | 0.249784 | intron-variant | MNAT1 | GRCh38.p7 | 14:60802501 | TTTGTAAACTGGGCT[C/G]TCAGTTAAGATTTTA | 4331 |
rs4902007 | snp | C/G | 0.252404 | 0.254941 | intron-variant | MNAT1 | GRCh38.p7 | 14:60802654 | GATATTTTAGACATA[C/G]AATATTCAAGTGGTT | 4331 |
rs4902009 | snp | A/C | 0.0107246 | 0.0724382 | intron-variant | MNAT1 | GRCh38.p7 | 14:60843882 | tcccccaagtcacaa[A/C]gataattctcctgtt | 4331 |
rs4902010 | snp | C/T | 0.237014 | 0.249662 | intron-variant | MNAT1 | GRCh38.p7 | 14:60862893 | AGAGTGTTCACATAA[C/T]GAAGGTAGGATATGA | 4331 |
rs4902012 | snp | A/G | 0.233235 | 0.249437 | intron-variant | MNAT1 | GRCh38.p7 | 14:60886270 | ttataatttttttct[A/G]tttgtattgaaaatg | 4331 |
rs4902014 | snp | A/G | 0.232067 | 0.249356 | intron-variant | MNAT1 | GRCh38.p7 | 14:60899984 | CCACAAACTGTACCC[A/G]TATAAGAAGGTGAAG | 4331 |
rs4902015 | snp | C/T | 0.197703 | 0.244469 | intron-variant | MNAT1 | GRCh38.p7 | 14:60900111 | ccctattccctgaga[C/T]gcagcaatattgaaa | 4331 |
rs4902017 | snp | C/T | 0.337841 | 0.23406 | intron-variant | MNAT1 | GRCh38.p7 | 14:60913311 | tttgatcttctgaag[C/T]cttcctctctcaact | 4331 |
rs4902018 | snp | G/T | 0.258288 | 0.249863 | intron-variant | MNAT1 | GRCh38.p7 | 14:60913452 | gttttccccatcttt[G/T]tggttttatctacct | 4331 |
rs4902019 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | MNAT1 | GRCh38.p7 | 14:60913465 | ttgtggttttatcta[C/T]cttgggtctttgatg | 4331 |
rs4902020 | snp | C/G | 0.204189 | 0.245767 | intron-variant | MNAT1 | GRCh38.p7 | 14:60920740 | TGAGCCACGACGCCT[C/G]GCCTTATATTCTCTT | 4331 |
rs5809070 | in-del | -/TG | 0.190519 | 0.242821 | intron-variant | MNAT1 | GRCh38.p7 | 14:60861573 | TTTTTTAAAAAAATT[-/TG]TGAAAAGGTCTACAG | 4331 |
rs5809071 | in-del | -/A | 0 | 0 | intron-variant | MNAT1 | GRCh38.p7 | 14:60924402 | AAAAAAAAAAAAAAA[-/A]CTGTACTCCATGCCT | 4331 |
rs5809072 | in-del | -/T | 0.252702 | 0.249985 | intron-variant | MNAT1 | GRCh38.p7 | 14:60924636 | TAACATCACCCTCCC[-/T]TGACTCTCAAAATAA | 4331 |
rs6573331 | snp | A/G | 0.228547 | 0.249078 | intron-variant | MNAT1 | GRCh38.p7 | 14:60771118 | ttactaggaaatgcc[A/G]ttttgttctttaaag | 4331 |
rs6573332 | snp | A/G | 0.19646 | 0.2442 | intron-variant | MNAT1 | GRCh38.p7 | 14:60826202 | ATTAAACTGTCAGGG[A/G]GTGGAGTAATGTTAG | 4331 |
rs6573333 | snp | G/T | 0.240765 | 0.249829 | intron-variant | MNAT1 | GRCh38.p7 | 14:60841619 | tgtcctttctgagtc[G/T]gcttctattgactga | 4331 |
rs6573338 | snp | A/G | 0.191461 | 0.24305 | intron-variant | MNAT1 | GRCh38.p7 | 14:60864335 | AAAATAGGGACAGTT[A/G]TGGTGGTATACTTTC | 4331 |
rs6573339 | snp | A/G | 0.202959 | 0.245534 | intron-variant | MNAT1 | GRCh38.p7 | 14:60875500 | CAATATCTAACCCCC[A/G]TTTCCTCATTCATAA | 4331 |
rs6573341 | snp | A/G | 0.262985 | 0.249663 | intron-variant | MNAT1 | GRCh38.p7 | 14:60901376 | ggatatgtgcaagga[A/G]atggatattgttttc | 4331 |
rs6573342 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | MNAT1 | GRCh38.p7 | 14:60910696 | gatcatggtggataa[A/G]ctttttgatgtgctg | 4331 |
rs6573344 | snp | A/G | 0.196771 | 0.244268 | intron-variant | MNAT1 | GRCh38.p7 | 14:60914131 | ctccgagcctggtgc[A/G]ggatataatctcctg | 4331 |
rs6573346 | snp | G/T | 0.454302 | 0.144085 | intron-variant | MNAT1 | GRCh38.p7 | 14:60917612 | agatttgagttttgt[G/T]ttttttttgtttctt | 4331 |
rs6573347 | snp | C/T | 0.302936 | 0.244331 | intron-variant | MNAT1 | GRCh38.p7 | 14:60935551 | ATCTTCTCTTATTTT[C/T]AGTATTTTAAATTCA | 4331 |
rs7141013 | snp | C/T | 0.295088 | 0.245901 | intron-variant | MNAT1 | GRCh38.p7 | 14:60953236 | TACAAATGTATTATA[C/T]GTATGTATATATGTA | 4331 |
rs7141362 | snp | A/G | 0.0663309 | 0.169604 | intron-variant | MNAT1 | GRCh38.p7 | 14:60748939 | catacgactggtggt[A/G]cagtaggtttgttta | 4331 |
rs7141927 | snp | C/G | 0.451732 | 0.147663 | intron-variant | MNAT1 | GRCh38.p7 | 14:60940520 | cctcccaggttcatg[C/G]cattcttctgcctca | 4331 |
rs7142069 | snp | C/G | 0.331179 | 0.236453 | intron-variant | MNAT1 | GRCh38.p7 | 14:60940542 | tctgcctcagcctcc[C/G]gagtagctgggacta | 4331 |
rs7142844 | snp | A/C | 0.468949 | 0.12067 | intron-variant | MNAT1 | GRCh38.p7 | 14:60766614 | ctactcgggaggctg[A/C]ggcacgagaattgct | 4331 |
rs7143411 | snp | A/G | 0.0418186 | 0.138422 | intron-variant | MNAT1 | GRCh38.p7 | 14:60752479 | AGAAAAAAATTATAC[A/G]TAATACTTTCACAGA | 4331 |
rs7144443 | snp | C/G | 0.191147 | 0.242974 | intron-variant | MNAT1 | GRCh38.p7 | 14:60784289 | tctgcctcccaaagt[C/G]ctgggattacaggca | 4331 |
rs7144534 | snp | G/T | 0.0279526 | 0.114869 | intron-variant | MNAT1 | GRCh38.p7 | 14:60752869 | tcctgggttggagca[G/T]ttctcctgcctcagc | 4331 |
rs7144606 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | MNAT1 | GRCh38.p7 | 14:60958698 | ctggagtgcagtggc[A/G]cgatcttggctcact | 4331 |
rs7146168 | snp | C/T | 0.0891348 | 0.19137 | intron-variant | MNAT1 | GRCh38.p7 | 14:60946514 | TTATGACACTACTTC[C/T]tttttgtttttgttt | 4331 |
rs7146466 | snp | C/T | 0.188946 | 0.24243 | intron-variant | MNAT1 | GRCh38.p7 | 14:60754624 | aaagtgctgggatta[C/T]aggcgtgagccaccg | 4331 |
rs7150085 | snp | A/C | | | intron-variant | MNAT1 | GRCh38.p7 | 14:60856085 | aagctagaaacgatt[A/C]agcttcctaaggaag | 4331 |
rs7150106 | snp | C/T | 0.232067 | 0.249356 | intron-variant | MNAT1 | GRCh38.p7 | 14:60901812 | tgagaaactgactct[C/T]agggatgagtaaaga | 4331 |
rs7150492 | snp | C/T | 0.228842 | 0.249103 | intron-variant | MNAT1 | GRCh38.p7 | 14:60901315 | agatttctttcaaaa[C/T]actgctactcattga | 4331 |
rs7150631 | snp | A/G | 0.247337 | 0.249986 | intron-variant | MNAT1 | GRCh38.p7 | 14:60910573 | gccttttctgcatct[A/G]ttgagataatcatgt | 4331 |
rs7151349 | snp | C/T | 0.190519 | 0.242821 | intron-variant | MNAT1 | GRCh38.p7 | 14:60747141 | aggtgcccgccacca[C/T]gcccggctaattttt | 4331 |
rs7151575 | snp | A/G | 0.18989 | 0.242666 | intron-variant | MNAT1 | GRCh38.p7 | 14:60755551 | CAAAGTGTTGGGATT[A/G]TAGGCTAGTCACTGC | 4331 |
rs7152185 | snp | A/T | 0 | 0 | intron-variant | MNAT1 | GRCh38.p7 | 14:60794660 | AAAAAAAAAAAAAAA[A/T]ATATATATATATATA | 4331 |
rs7153035 | snp | A/G | 0.242775 | 0.249896 | intron-variant | MNAT1 | GRCh38.p7 | 14:60794937 | TAGTGAGTACTTAGC[A/G]TTAGGCACTGCGGAT | 4331 |
rs7153072 | snp | G/T | 0.0310518 | 0.120672 | intron-variant | MNAT1 | GRCh38.p7 | 14:60903845 | TAAGTTTTGTTTTGT[G/T]TTTGATGCTACCCAT | 4331 |
rs7155205 | snp | A/T | 0.232359 | 0.249377 | intron-variant | MNAT1 | GRCh38.p7 | 14:60902308 | caatgaagactgtca[A/T]attgatggtcctatt | 4331 |
rs7155712 | snp | C/T | 0.0912534 | 0.193131 | intron-variant | MNAT1 | GRCh38.p7 | 14:60807352 | AGCAATCTGTAGAAA[C/T]CCAAGGGATAGAGCA | 4331 |
rs7156087 | snp | C/T | 0.332337 | 0.236052 | intron-variant | MNAT1 | GRCh38.p7 | 14:60935600 | TGTGTTATGGGCACA[C/T]AATGTGTTTGGACAT | 4331 |
rs7160499 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | MNAT1 | GRCh38.p7 | 14:60900112 | cctattccctgagat[A/G]cagcaatattgaaat | 4331 |
rs7160578 | snp | C/G | 0 | 0 | intron-variant | MNAT1 | GRCh38.p7 | 14:60936404 | cccacaacaggcccc[C/G]gtgtgtgatgttccc | 4331 |
rs7161360 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | MNAT1 | GRCh38.p7 | 14:60908456 | aggtatatcttctaa[C/T]gctatccctccccca | 4331 |
rs7492782 | snp | C/T | 0 | 0 | intron-variant | MNAT1 | GRCh38.p7 | 14:60824415 | ATATGATTGTGGCTA[C/T]GTAGGTACTTAAATA | 4331 |
rs7493682 | snp | A/T | 0.197082 | 0.244335 | intron-variant | MNAT1 | GRCh38.p7 | 14:60914125 | aggaccctccgagcc[A/T]ggtgcaggatataat | 4331 |
rs8003035 | snp | C/T | 0.375 | 0.216506 | intron-variant | MNAT1 | GRCh38.p7 | 14:60805224 | GTTTTTTCTTTTTTC[C/T]TTTtttttaaaagta | 4331 |
rs8003057 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | MNAT1 | GRCh38.p7 | 14:60857690 | tcaacttgtcattta[C/G]attagttatttctcc | 4331 |
rs8003554 | snp | A/C | 0.143284 | 0.226079 | intron-variant | MNAT1 | GRCh38.p7 | 14:60912306 | TCTTTTAATTGGAGC[A/C]TTTAGCCCATTTACA | 4331 |
rs8003622 | snp | A/G | 0.264358 | 0.249587 | intron-variant | MNAT1 | GRCh38.p7 | 14:60896433 | TGATACAAATCATGA[A/G]CATTTGTGACACAAC | 4331 |
rs8004224 | snp | A/C | 0.100588 | 0.200439 | intron-variant | MNAT1 | GRCh38.p7 | 14:60882537 | tgaacagtcctgtaa[A/C]aaacatgggagtgca | 4331 |
rs8004671 | snp | C/G | 0.257454 | 0.249889 | intron-variant | MNAT1 | GRCh38.p7 | 14:60822401 | GGCAAAGTTGCTTCA[C/G]CAGCATACTTTTTAA | 4331 |
rs8004789 | snp | A/C | 0.197082 | 0.244335 | intron-variant | MNAT1 | GRCh38.p7 | 14:60882922 | ttttgcccattttta[A/C]gttggattattacat | 4331 |
rs8005182 | snp | C/T | 0.226188 | 0.248863 | intron-variant | MNAT1 | GRCh38.p7 | 14:60861355 | AATTATTTAAAACAT[C/T]TTCCTTAGAACTGGA | 4331 |
rs8005350 | snp | A/T | | | intron-variant | MNAT1 | GRCh38.p7 | 14:60828226 | taattactcaactct[A/T]aaaaaagagattatg | 4331 |
rs8005602 | snp | A/G | 0.197082 | 0.244335 | intron-variant | MNAT1 | GRCh38.p7 | 14:60883088 | ttttaacttgatgtg[A/G]tcctacttacctatt | 4331 |
rs8011093 | snp | A/C | 0.239037 | 0.24976 | intron-variant | MNAT1 | GRCh38.p7 | 14:60876830 | GTTTATTCATTTATT[A/C]CTTGATGGACACTGC | 4331 |
rs8011729 | snp | A/G | 0.120326 | 0.21374 | intron-variant | MNAT1 | GRCh38.p7 | 14:60877014 | AGGACGTGCCATACC[A/G]TTTTCCACAGCAGCT | 4331 |
rs8012779 | snp | C/T | 0.29278 | 0.246313 | intron-variant | MNAT1 | GRCh38.p7 | 14:60964898 | TAAAATACTTCGACA[C/T]GCTACAATAATTAAA | 4331 |
rs8013288 | snp | C/T | | | intron-variant | MNAT1 | GRCh38.p7 | 14:60746925 | atatatatatatata[C/T]acacacacacacaca | 4331 |
rs8013435 | snp | C/T | 0.19646 | 0.2442 | intron-variant | MNAT1 | GRCh38.p7 | 14:60873351 | GCCATAAATATAAAA[C/T]ATACCCATTTTATAC | 4331 |
rs8013545 | snp | A/T | 0.481165 | 0.0951993 | intron-variant | MNAT1 | GRCh38.p7 | 14:60863100 | GAAAATGCAGTCTTA[A/T]ACAGTATGATTCTTT | 4331 |
rs8015531 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | MNAT1 | GRCh38.p7 | 14:60820950 | AAATGGAGTTAGCCA[G/T]GCAAAAATACAGGCA | 4331 |
rs8016715 | snp | A/G | 0.276267 | 0.248616 | intron-variant | MNAT1 | GRCh38.p7 | 14:60951321 | TGTCTTATTGTTATT[A/G]TTGTTTTTGGCTCAT | 4331 |
rs8016726 | snp | C/T | 0.188946 | 0.24243 | intron-variant | MNAT1 | GRCh38.p7 | 14:60768336 | CTTCAATAGTATTTG[C/T]AATTTTGAAGAGTTA | 4331 |
rs8017374 | snp | A/G | 0.115438 | 0.210697 | intron-variant | MNAT1 | GRCh38.p7 | 14:60935945 | tgagtagaacaggat[A/G]ttattaggctaaaag | 4331 |
rs8017608 | snp | A/T | 0.0836354 | 0.186609 | intron-variant | MNAT1 | GRCh38.p7 | 14:60743963 | ttcatttctctgata[A/T]ttcccatctatatac | 4331 |
rs8017883 | snp | A/T | 0.198014 | 0.244535 | intron-variant | MNAT1 | GRCh38.p7 | 14:60747411 | tatacctaagctata[A/T]ggtgtagcttattgc | 4331 |
rs8017941 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | MNAT1 | GRCh38.p7 | 14:60856645 | tttttagaggctaat[A/G]cagctggtgacttta | 4331 |
rs8017962 | snp | A/G | 0.0414363 | 0.137845 | intron-variant | MNAT1 | GRCh38.p7 | 14:60807388 | ATTTAGGGTAGATCC[A/G]TCTTGTTTGTAGGGC | 4331 |
rs8018438 | snp | A/G | 0.189576 | 0.242588 | intron-variant | MNAT1 | GRCh38.p7 | 14:60857220 | TGTACGAGGAGATGA[A/G]GGTTGTTTTCAAAAT | 4331 |
rs8018928 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | MNAT1 | GRCh38.p7 | 14:60930708 | ACAGAAGGATTCAGA[A/G]ATTTGACAGAACAGG | 4331 |
rs8019418 | snp | C/G | 0 | 0 | intron-variant | MNAT1 | GRCh38.p7 | 14:60911828 | gagttctgtagatgt[C/G]tattaggtccgcttg | 4331 |
rs8019538 | snp | G/T | | | intron-variant | MNAT1 | GRCh38.p7 | 14:60887232 | TTTTTGTTTGTTTTT[G/T]GTTTTTAttttattt | 4331 |
rs8019589 | snp | A/G | 0.196771 | 0.244268 | intron-variant | MNAT1 | GRCh38.p7 | 14:60881815 | ATTTTAGTTATTTTC[A/G]AATGTACAATTAAAT | 4331 |
rs8019844 | snp | A/T | | | intron-variant | MNAT1 | GRCh38.p7 | 14:60827174 | AAAGATAAAAGTACT[A/T]AAAAACAAAAGAATT | 4331 |
rs8019883 | snp | A/G | 0.211212 | 0.246973 | intron-variant | MNAT1 | GRCh38.p7 | 14:60836168 | TCTTAGCTTCCTTGC[A/G]TTGGGTTATATCATG | 4331 |
rs8020097 | snp | C/G | 0.331642 | 0.236293 | intron-variant | MNAT1 | GRCh38.p7 | 14:60940010 | TTTGTCTCTCTTGAT[C/G]TTTGTTGGTTTAAAG | 4331 |
rs8020235 | snp | A/G | 0.189261 | 0.242509 | intron-variant | MNAT1 | GRCh38.p7 | 14:60772668 | AGATTAGAAACTCAG[A/G]TTGCATTAGTGGTTT | 4331 |
rs8021571 | snp | A/T | 0.00874735 | 0.0655527 | intron-variant | MNAT1 | GRCh38.p7 | 14:60845100 | gtaatataatgtttt[A/T]atcagtaatgctagc | 4331 |
rs8022005 | snp | A/G | 0.191147 | 0.242974 | intron-variant | MNAT1 | GRCh38.p7 | 14:60878663 | tattttgaattgtga[A/G]ttttttgaattgttg | 4331 |
rs8022056 | snp | C/T | | | intron-variant | MNAT1 | GRCh38.p7 | 14:60805223 | AGTTTTTTCTTTTTT[C/T]TTTTtttttaaaagt | 4331 |
rs8022875 | snp | C/T | 0.236434 | 0.249632 | intron-variant | MNAT1 | GRCh38.p7 | 14:60848305 | ATTGTGTGTGATAAG[C/T]ATTTTCTCTTTTGCT | 4331 |
rs8022908 | snp | G/T | 0.197393 | 0.244402 | intron-variant | MNAT1 | GRCh38.p7 | 14:60887352 | CATTAACTCGTCATT[G/T]AGCATTAGGTATATC | 4331 |
rs8023097 | snp | A/T | 0.0252325 | 0.109451 | intron-variant | MNAT1 | GRCh38.p7 | 14:60915390 | atggtgaatatgaaa[A/T]tcttattttcagctg | 4331 |
rs9285588 | snp | A/G | 0.150667 | 0.229419 | intron-variant | MNAT1 | GRCh38.p7 | 14:60847354 | ggttgcagtgagcca[A/G]gatcgcaccactgca | 4331 |
rs9323366 | snp | C/T | 0.230017 | 0.2492 | intron-variant | MNAT1 | GRCh38.p7 | 14:60771880 | gaatTGCTTTGAATT[C/T]GGTGAAAAAGTGTCC | 4331 |
rs9670725 | snp | C/T | 0.0584853 | 0.160693 | intron-variant | MNAT1 | GRCh38.p7 | 14:60939621 | ataatttctgttctt[C/T]tacatttgctgagga | 4331 |
rs9672031 | snp | C/T | 0.477853 | 0.102875 | intron-variant | MNAT1 | GRCh38.p7 | 14:60953700 | TTTTTGAGGAACTTC[C/T]GTACTGTTTTCCATG | 4331 |
rs9672053 | snp | G/T | 0.19646 | 0.2442 | intron-variant | MNAT1 | GRCh38.p7 | 14:60739186 | GATTGGAGAGATGGA[G/T]GGGAGAAGAGAGAAA | 4331 |
rs9743607 | snp | A/C | 0.281841 | 0.247964 | intron-variant | MNAT1 | GRCh38.p7 | 14:60938408 | tatgtcccatcaata[A/C]ctaatttattgagag | 4331 |
rs9743735 | snp | C/G | | | intron-variant | MNAT1 | GRCh38.p7 | 14:60887717 | aagactaataaagaa[C/G]aaaagagagaagaat | 4331 |
rs9972218 | snp | G/T | 0.241053 | 0.24984 | intron-variant | MNAT1 | GRCh38.p7 | 14:60888769 | aggatacaaaatcaa[G/T]gtacaaaaatcacaa | 4331 |
rs9972243 | snp | A/G | | | intron-variant | MNAT1 | GRCh38.p7 | 14:60860150 | CTTTCAGGCTTTTGG[A/G]AGTTAGTGATTTTAT | 4331 |
rs10130274 | snp | G/T | 0.00835141 | 0.0640778 | intron-variant | MNAT1 | GRCh38.p7 | 14:60923069 | TTTCTTTCCCATATT[G/T]GTGAATAAAATTGAG | 4331 |
rs10130717 | snp | C/T | 0.29432 | 0.24604 | intron-variant | MNAT1 | GRCh38.p7 | 14:60949554 | ATACCAGCATGTGCA[C/T]AGTTACAAGGCATTG | 4331 |
rs10130814 | snp | A/G | 0.190833 | 0.242898 | intron-variant | MNAT1 | GRCh38.p7 | 14:60824585 | GAAAATGGGCATAAC[A/G]GGATTAAATCCCAGA | 4331 |
rs10130819 | snp | A/G | 0.121369 | 0.214369 | intron-variant | MNAT1 | GRCh38.p7 | 14:60824598 | ACAGGATTAAATCCC[A/G]GATTTACCGTTATTA | 4331 |
rs10131264 | snp | G/T | 0.230896 | 0.249269 | intron-variant | MNAT1 | GRCh38.p7 | 14:60815839 | CACTGCAGTTTGAAT[G/T]TCTGGTTTTCATTTT | 4331 |
rs10132758 | snp | A/T | 0.191461 | 0.24305 | intron-variant | MNAT1 | GRCh38.p7 | 14:60800622 | AGCAAAACTCTAAAA[A/T]CTAGAATTTGCTCTA | 4331 |
rs10133880 | snp | A/C | 0.332337 | 0.236052 | intron-variant | MNAT1 | GRCh38.p7 | 14:60943321 | CTAATATGAACACTC[A/C]TAAAATTTCAGAGCA | 4331 |
rs10134410 | snp | C/G | 0.188946 | 0.24243 | intron-variant | MNAT1 | GRCh38.p7 | 14:60768085 | TTTGTATTTTTAGTA[C/G]AGTCAGTGTTTCGCC | 4331 |
rs10134967 | snp | C/T | 0.114387 | 0.210022 | intron-variant | MNAT1 | GRCh38.p7 | 14:60762687 | ctccattctgggcaa[C/T]agagcgagactctgt | 4331 |
rs10135373 | snp | A/G | 0.121369 | 0.214369 | intron-variant | MNAT1 | GRCh38.p7 | 14:60813653 | tttagtccacACAGT[A/G]TGTACTGGGGAAAAC | 4331 |
rs10135867 | snp | A/G | 0.18989 | 0.242666 | intron-variant | MNAT1 | GRCh38.p7 | 14:60844000 | gtttcttttttgcat[A/G]tgaacatttagttgt | 4331 |
rs10136048 | snp | G/T | 0.235564 | 0.249583 | intron-variant | MNAT1 | GRCh38.p7 | 14:60844210 | ttctttttcaagatt[G/T]ctttttgcatatcct | 4331 |
rs10137397 | snp | C/T | 0.232067 | 0.249356 | intron-variant | MNAT1 | GRCh38.p7 | 14:60907722 | AGGAGGCAGAGGTTG[C/T]GGTGAGCCAAGATTG | 4331 |
rs10137978 | snp | C/G | 0.197393 | 0.244402 | intron-variant | MNAT1 | GRCh38.p7 | 14:60911441 | ttttagatctttcct[C/G]ctttctcttgtgggc | 4331 |
rs10140004 | snp | A/T | 0 | 0 | intron-variant | MNAT1 | GRCh38.p7 | 14:60918758 | TATATATATATATAT[A/T]TTTGTCCTTAAAAAT | 4331 |
rs10140419 | snp | C/G | 0.121022 | 0.21416 | intron-variant | MNAT1 | GRCh38.p7 | 14:60857423 | aatctcatgataaaa[C/G]ttgaatggatgagga | 4331 |
rs10141418 | snp | C/G | 0.204496 | 0.245824 | intron-variant | MNAT1 | GRCh38.p7 | 14:60923240 | AAAGATTGCTGGGCC[C/G]CACCTTCAGAGTTTG | 4331 |
rs10142922 | snp | A/G | 0.18989 | 0.242666 | intron-variant | MNAT1 | GRCh38.p7 | 14:60775573 | cataatgcaggagaa[A/G]ggggagataattata | 4331 |
rs10142977 | snp | A/C/G | 0.00119737 | 0.0244387 | intron-variant | MNAT1 | GRCh38.p7 | 14:60863447 | AAATGCAGCTGATTG[A/C/G]CAGTAGCATCTGTCT | 4331 |
rs10144292 | snp | G/T | 0.327211 | 0.237778 | intron-variant | MNAT1 | GRCh38.p7 | 14:60819774 | ACCCATTTATCCAGC[G/T]GCTTGACATGAACAA | 4331 |
rs10147575 | snp | A/C | 0.200492 | 0.245049 | intron-variant | MNAT1 | GRCh38.p7 | 14:60890164 | cacatatgtttattg[A/C]ggcactattcacaat | 4331 |
rs10148178 | snp | A/G | 0.252702 | 0.249985 | intron-variant | MNAT1 | GRCh38.p7 | 14:60877411 | GATGCAAGGATCTTC[A/G]ATGGTTGTTTCTCAC | 4331 |
rs10148248 | snp | A/G | 0.120326 | 0.21374 | intron-variant | MNAT1 | GRCh38.p7 | 14:60817252 | TATAAAATTCTTAAT[A/G]TAAATCTAGAATAGC | 4331 |
rs10148902 | snp | A/G | 0.232359 | 0.249377 | intron-variant | MNAT1 | GRCh38.p7 | 14:60908227 | TAAAGATTATTTTAC[A/G]TTTAAATTTTTTTAT | 4331 |
rs10150605 | snp | C/T | 0.252702 | 0.249985 | intron-variant | MNAT1 | GRCh38.p7 | 14:60773036 | TCTGACTCCCTGGTT[C/T]AAGCGATTCTCCTAC | 4331 |
rs10467730 | snp | A/C | 0.0858192 | 0.188533 | intron-variant | MNAT1 | GRCh38.p7 | 14:60938416 | atcaataactaattt[A/C]ttgagagtttttagc | 4331 |
rs10467807 | snp | A/G | 0.231775 | 0.249335 | intron-variant | MNAT1 | GRCh38.p7 | 14:60901896 | tgaaatgacaacaaa[A/G]gatttagaatattat | 4331 |
rs10467809 | snp | A/C | 0.111928 | 0.208413 | intron-variant | MNAT1 | GRCh38.p7 | 14:60936982 | tgatggccagtgatg[A/C]tgagcattttttcat | 4331 |
rs10467810 | snp | C/G | 0.283947 | 0.247685 | intron-variant | MNAT1 | GRCh38.p7 | 14:60937038 | tcttttgagaagtgt[C/G]tgttcatatccttca | 4331 |
rs10467811 | snp | A/G | 0.281313 | 0.248031 | intron-variant | MNAT1 | GRCh38.p7 | 14:60937053 | gtgttcatatccttc[A/G]cccacttgttgatgg | 4331 |
rs10782442 | snp | A/G | 0.190833 | 0.242898 | intron-variant | MNAT1 | GRCh38.p7 | 14:60836857 | CTCCCCTTCCCCAAG[A/G]TGCTCTGTCCTAGGG | 4331 |
rs10873129 | snp | A/T | 0.0356815 | 0.128715 | intron-variant | MNAT1 | GRCh38.p7 | 14:60962306 | AATTTATCAAATATC[A/T]TTTGGCCTATTAGCT | 4331 |
rs11158310 | snp | G/T | 0.449218 | 0.151037 | intron-variant | MNAT1 | GRCh38.p7 | 14:60918486 | gtggtgggattagag[G/T]catgagccacagtgc | 4331 |
rs11158313 | snp | A/T | 0.279195 | 0.248289 | intron-variant | MNAT1 | GRCh38.p7 | 14:60954405 | aatgtctttcatcag[A/T]gttttatagttttca | 4331 |
rs11158314 | snp | C/G | 0.499793 | 0.0101816 | intron-variant | MNAT1 | GRCh38.p7 | 14:60954414 | catcagagttttata[C/G]ttttcagtgtataga | 4331 |
rs11296750 | in-del | -/A | 0.217551 | 0.247885 | intron-variant | MNAT1 | GRCh38.p7 | 14:60746515 | GTGAGACTCTGTCTC[-/A]AAAAAAAAAAAAGAA | 4331 |
rs11350105 | in-del | -/A | 0.20511 | 0.245937 | intron-variant | MNAT1 | GRCh38.p7 | 14:60917305 | CCTCATTTTACCAGG[-/A]AAAAATAGTCATTCC | 4331 |
rs11351310 | in-del | -/T | 0.32955 | 0.237006 | intron-variant | MNAT1 | GRCh38.p7 | 14:60873654 | TTTTTTTTTTTTTTT[-/T]GTAGAGATGGCTCAC | 4331 |
rs11359127 | in-del | -/T | 0 | 0 | intron-variant | MNAT1 | GRCh38.p7 | 14:60959937 | TTTTTTTTTTTTTTT[-/T]GCTAAGCATTGTTTC | 4331 |
rs11409940 | in-del | -/T | | | intron-variant | MNAT1 | GRCh38.p7 | 14:60860370 | TTTTTTTTTTTTTTT[-/T]GAGACAGAGTCTTAC | 4331 |
rs11418104 | in-del | -/A/AA | 0 | 0 | intron-variant | MNAT1 | GRCh38.p7 | 14:60914567 | TGGTAAAAAAAAAAA[-/A/AA]TCTGTTCTGGCTGTC | 4331 |
rs11434422 | in-del | -/T | 0 | 0 | intron-variant | MNAT1 | GRCh38.p7 | 14:60903142 | TTTAAGTGTTTTTTT[-/T]GTATCACATATATGT | 4331 |
rs11621846 | snp | A/G | 0.5 | 0 | intron-variant | MNAT1 | GRCh38.p7 | 14:60849962 | ccgcctcagcctcct[A/G]agtggctgggattac | 4331 |
rs11623173 | snp | G/T | 0.444444 | 0.157135 | intron-variant | MNAT1 | GRCh38.p7 | 14:60843762 | tttttctttttctta[G/T]taatgttttttgatg | 4331 |
rs11623289 | snp | A/T | 0.18989 | 0.242666 | intron-variant | MNAT1 | GRCh38.p7 | 14:60859253 | CTATCTTGGTAGGTC[A/T]TGAGATGTCTAGCCA | 4331 |
rs11623438 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | MNAT1 | GRCh38.p7 | 14:60926478 | TTGGGGGTTCCCACA[A/G]ACCATTCGTCAGTTT | 4331 |
rs11623446 | snp | A/G | 0.266273 | 0.24947 | intron-variant | MNAT1 | GRCh38.p7 | 14:60926527 | ggctcacagaactca[A/G]ggaaacactttactt | 4331 |
rs11625511 | snp | C/T | 0.2776 | 0.248472 | intron-variant | MNAT1 | GRCh38.p7 | 14:60940541 | TTCTGCCTCAGCCTC[C/T]CGAGTAGCTGGGACT | 4331 |
rs11626352 | snp | G/T | 0 | 0 | intron-variant | MNAT1 | GRCh38.p7 | 14:60793570 | agagggagggatcta[G/T]ccatgttgtctaggc | 4331 |
rs11628101 | snp | A/C | 0.257732 | 0.24988 | intron-variant | MNAT1 | GRCh38.p7 | 14:60908197 | TTTAGTTTGTTACTT[A/C]TTTCTTTCATGATAT | 4331 |
rs11628306 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MNAT1 | GRCh38.p7 | 14:60768396 | TTTTAAAGGTCTTGG[C/T]TGACTTCTTAAAAGT | 4331 |
rs11628374 | snp | C/T | 0 | 0 | intron-variant | MNAT1 | GRCh38.p7 | 14:60826315 | AGGAGAAATTTTTTT[C/T]TTTTTTTTTTTTTTT | 4331 |
rs11629236 | snp | A/C | | | intron-variant | MNAT1 | GRCh38.p7 | 14:60783695 | tagagacagggtttc[A/C]ccgtgttagccagga | 4331 |
rs11846280 | snp | G/T | 0 | 0 | intron-variant | MNAT1 | GRCh38.p7 | 14:60841890 | gtatttattgagagg[G/T]ctttttaccttgttt | 4331 |
rs11846592 | snp | A/C | | | intron-variant | MNAT1 | GRCh38.p7 | 14:60773626 | ACCTGTTAGGAAGGG[A/C]TAGACAGTAATGTAA | 4331 |
rs11846727 | snp | C/T | | | intron-variant | MNAT1 | GRCh38.p7 | 14:60751133 | TGGGGAAACTGAAGC[C/T]TAAGAAAGGATATAT | 4331 |
rs11849230 | snp | C/T | 0.375 | 0.216506 | intron-variant | MNAT1 | GRCh38.p7 | 14:60793486 | tcctgcctcagcctc[C/T]tgagtagctaggact | 4331 |
rs11850260 | snp | A/G | 0.0490535 | 0.14873 | intron-variant | MNAT1 | GRCh38.p7 | 14:60959987 | tgcatgtacatagct[A/G]taacttatttatttt | 4331 |
rs12147352 | snp | A/C | 0.279461 | 0.248258 | intron-variant | MNAT1 | GRCh38.p7 | 14:60951924 | ATTCTTAATTTTTTG[A/C]GGGTGGAGCAGGCTT | 4331 |
rs12147818 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MNAT1 | GRCh38.p7 | 14:60772063 | GATGAATTAAAGAGC[A/G]CATTTTTAAGGGCTC | 4331 |
rs12433770 | snp | A/G | 0.197703 | 0.244469 | intron-variant | MNAT1 | GRCh38.p7 | 14:60911574 | ttctgccttcatttc[A/G]ttgtgtacccagtag | 4331 |
rs12434584 | snp | C/T | 0.369346 | 0.219673 | intron-variant | MNAT1 | GRCh38.p7 | 14:60858036 | gcctcagtaaacata[C/T]gtgtgcatgtgtctt | 4331 |
rs12435775 | snp | C/G | | | intron-variant | MNAT1 | GRCh38.p7 | 14:60746256 | tgcggtagctcacac[C/G]tgtaatcccagcgct | 4331 |
rs12436792 | snp | A/G | 0.450105 | 0.149859 | intron-variant | MNAT1 | GRCh38.p7 | 14:60842902 | agcatcctattgcat[A/G]ttgctagcccaggaa | 4331 |
rs12587061 | snp | A/G | 0.311369 | 0.242351 | intron-variant | MNAT1 | GRCh38.p7 | 14:60862272 | TATAACTGTTAGCAC[A/G]TATGCTTTGTGTGCT | 4331 |
rs12588140 | snp | C/T | 0 | 0 | intron-variant | MNAT1 | GRCh38.p7 | 14:60872871 | ACACACACACACACA[C/T]ATATATATGCACTTT | 4331 |
rs12590111 | snp | C/T | 0 | 0 | intron-variant | MNAT1 | GRCh38.p7 | 14:60918145 | taattgcaaaagatt[C/T]tcacttttagatttg | 4331 |
rs12590229 | snp | G/T | 0 | 0 | intron-variant | MNAT1 | GRCh38.p7 | 14:60750772 | GGTTGGGTACAGGTT[G/T]TGCAAAGTTAGCATC | 4331 |
rs12590768 | snp | A/G | 0.191461 | 0.24305 | intron-variant | MNAT1 | GRCh38.p7 | 14:60831063 | CCTCCATTCCTAATG[A/G]TGGCTAGAGCTAAGA | 4331 |
rs12878060 | snp | G/T | | | intron-variant | MNAT1 | GRCh38.p7 | 14:60936433 | cccttcctgtgtccg[G/T]gtgttctcattgttc | 4331 |
rs12878775 | snp | A/T | 0.0429648 | 0.14013 | intron-variant | MNAT1 | GRCh38.p7 | 14:60784015 | attttttattttatt[A/T]atttaatttgagatg | 4331 |
rs12879072 | snp | A/T | 0.00795532 | 0.062565 | intron-variant | MNAT1 | GRCh38.p7 | 14:60857597 | tttattattatactt[A/T]aagttctgcggtaca | 4331 |
rs12881155 | snp | A/G | | | intron-variant | MNAT1 | GRCh38.p7 | 14:60919826 | GAGGGGTACTACCTC[A/G]CCTTGCACAGGATGC | 4331 |
rs12881166 | snp | A/G | | | intron-variant | MNAT1 | GRCh38.p7 | 14:60919838 | CTCACCTTGCACAGG[A/G]TGCCCTTGTTCCTGT | 4331 |
rs12881549 | snp | G/T | 0 | 0 | intron-variant | MNAT1 | GRCh38.p7 | 14:60845837 | tttgtgcttcatcct[G/T]gttttagtgtgGCTT | 4331 |
rs12881708 | snp | A/T | 0 | 0 | intron-variant | MNAT1 | GRCh38.p7 | 14:60845868 | TGTTAGACTTTAGTA[A/T]GAGGATAATATTGAC | 4331 |
rs12881725 | snp | C/T | | | intron-variant | MNAT1 | GRCh38.p7 | 14:60831453 | tgttcctgtgttagt[C/T]tgctgagaatgatgg | 4331 |
rs12881751 | snp | G/T | 0 | 0 | intron-variant | MNAT1 | GRCh38.p7 | 14:60845935 | TGCTTTCTAGAAGAG[G/T]TTCTGAACCATTGGT | 4331 |
rs12881885 | snp | A/T | 0 | 0 | intron-variant | MNAT1 | GRCh38.p7 | 14:60845952 | TCTGAACCATTGGTA[A/T]TATTTTTTCTTGAAA | 4331 |
rs12882075 | snp | C/T | | | intron-variant | MNAT1 | GRCh38.p7 | 14:60784275 | gtgatccacccgcct[C/T]tgcctcccaaagtcc | 4331 |
rs12882100 | snp | C/G | | | intron-variant | MNAT1 | GRCh38.p7 | 14:60784315 | aggcatgagccactg[C/G]gcccagccacccagc | 4331 |
rs12882543 | snp | A/T | | | intron-variant | MNAT1 | GRCh38.p7 | 14:60919839 | TCACCTTGCACAGGA[A/T]GCCCTTGTTCCTGTC | 4331 |
rs12882793 | snp | A/T | | | intron-variant | MNAT1 | GRCh38.p7 | 14:60929170 | aaaaaaaaaaaaaaa[A/T]atatatatatatata | 4331 |
rs12884883 | snp | A/T | 0.18989 | 0.242666 | intron-variant | MNAT1 | GRCh38.p7 | 14:60755181 | TTTTTTTTTTTTTAG[A/T]TGCCCAGGCTGGAAT | 4331 |
rs12888332 | snp | G/T | 0.021333 | 0.101051 | intron-variant | MNAT1 | GRCh38.p7 | 14:60894377 | CCTCCTCATCTTTCT[G/T]TTTTAGTCTTCTATG | 4331 |
rs12889328 | snp | A/G | 0.317451 | 0.240729 | intron-variant | MNAT1 | GRCh38.p7 | 14:60801703 | aggatatggagaaaa[A/G]ggaatccttgtatgc | 4331 |
rs12889598 | snp | A/G | 0.289165 | 0.246913 | intron-variant | MNAT1 | GRCh38.p7 | 14:60917564 | ATATGCAACTTGTAT[A/G]TGTTGAATCCATATT | 4331 |
rs12891034 | snp | G/T | | | intron-variant | MNAT1 | GRCh38.p7 | 14:60810544 | tatgctatgtttttg[G/T]ttttgtttgtcctga | 4331 |
rs12891347 | snp | A/G | 0.191775 | 0.243125 | intron-variant | MNAT1 | GRCh38.p7 | 14:60781155 | ATGTAACTTGAACCT[A/G]TGAAGGGATGGATAT | 4331 |
rs12891663 | snp | C/T | 0.232067 | 0.249356 | intron-variant | MNAT1 | GRCh38.p7 | 14:60907932 | ATATTTCCTAGTTAT[C/T]TGAATATCTGTTTCT | 4331 |
rs12892048 | snp | G/T | | | intron-variant | MNAT1 | GRCh38.p7 | 14:60918196 | caatccaattaattg[G/T]tcttttttttttttt | 4331 |
rs12892050 | snp | C/T | | | intron-variant | MNAT1 | GRCh38.p7 | 14:60918199 | tccaattaattgttc[C/T]ttttttttttttttt | 4331 |
rs12892680 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | MNAT1 | GRCh38.p7 | 14:60847622 | gtatatttctcatgg[A/G/T]gctttttgttcttct | 4331 |
rs12892693 | snp | G/T | | | intron-variant | MNAT1 | GRCh38.p7 | 14:60826505 | tttgtattttcagta[G/T]agacggggtttcacc | 4331 |
rs12894310 | snp | C/T | | | intron-variant | MNAT1 | GRCh38.p7 | 14:60851724 | acccaccaacaggcc[C/T]tggtgtgtgatgttc | 4331 |
rs12895213 | snp | C/T | 0.0329836 | 0.124112 | intron-variant | MNAT1 | GRCh38.p7 | 14:60844287 | aaagtataattgata[C/T]tctgattggatctat | 4331 |
rs12895490 | snp | G/T | 0 | 0 | intron-variant | MNAT1 | GRCh38.p7 | 14:60911870 | agttcaattcctgga[G/T]atccttgttaacttt | 4331 |
rs12896766 | snp | G/T | 0 | 0 | intron-variant | MNAT1 | GRCh38.p7 | 14:60869348 | acctggccTATATTG[G/T]TATATTTTTATATTA | 4331 |
rs12896928 | snp | C/G | | | intron-variant | MNAT1 | GRCh38.p7 | 14:60966304 | tttctatttttagta[C/G]agacggggtttcacc | 4331 |
rs13379338 | snp | A/G | 0.149665 | 0.228982 | intron-variant | MNAT1 | GRCh38.p7 | 14:60758785 | TCTGGAGGTGCAACT[A/G]GAAGTGTCGCTTTGA | 4331 |
rs17097774 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | MNAT1 | GRCh38.p7 | 14:60764412 | TGACTGTTTTTGTCT[A/G]TCAGATAGTGAAGCT | 4331 |
rs17097788 | snp | C/T | 0.14933 | 0.228835 | intron-variant, upstream-variant-2KB | MNAT1 | GRCh38.p7 | 14:60791674 | GGATCCCGTGGCTAA[C/T]TGGCTTGAAATCCAT | 4331 |
rs17097829 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | MNAT1 | GRCh38.p7 | 14:60859496 | AATCAGATTTTTACA[C/T]TGGGAAATATGAAGA | 4331 |
rs17097842 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | MNAT1 | GRCh38.p7 | 14:60863268 | TAACTAAGTAGATGC[A/G]TAGCTTACCTGGGGT | 4331 |
rs17097847 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | MNAT1 | GRCh38.p7 | 14:60865567 | TTATAGAAACAGATA[C/T]GGTTTGCTGGACACT | 4331 |
rs17097855 | snp | A/T | 0.0130921 | 0.0798413 | intron-variant | MNAT1 | GRCh38.p7 | 14:60875065 | ACTTTGTCTTATCGT[A/T]CTTATGGCAAACAGA | 4331 |
rs17097856 | snp | A/G | 0.0998734 | 0.199905 | intron-variant | MNAT1 | GRCh38.p7 | 14:60875126 | AAATGTTATAGTTTT[A/G]AAAAATACTCCTTTT | 4331 |
rs17097860 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | MNAT1 | GRCh38.p7 | 14:60880284 | TGTTGAAAGGTATAA[C/T]GTAAGGCTGGCCCTG | 4331 |
rs17256107 | snp | A/G | 0.459801 | 0.135955 | intron-variant | MNAT1 | GRCh38.p7 | 14:60762073 | TGTTTTACTGATTCT[A/G]TTTTTCTTCAAGTTT | 4331 |
rs17834418 | snp | G/T | 0.0136048 | 0.0813469 | intron-variant, upstream-variant-2KB | MNAT1 | GRCh38.p7 | 14:60797607 | GAATTGCATTTTTGG[G/T]CTGGTTACAAACCTG | 4331 |
rs28414277 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | MNAT1 | GRCh38.p7 | 14:60740022 | AGCTGGGTGTGGTGG[C/T]ATGGGCATGTAATCC | 4331 |
rs28813167 | snp | A/G | 0.306182 | 0.243605 | intron-variant | MNAT1 | GRCh38.p7 | 14:60938500 | CATGTGTTTTTTGTC[A/G]TTGGTTCTGTTAATA | 4331 |
rs28815000 | snp | A/C/G/T | 0.00199481 | 0.0315187 | intron-variant | MNAT1 | GRCh38.p7 | 14:60887389 | TGCTATCCCTCCCCC[A/C/G/T]TCCCCCCACCCCACA | 4331 |
rs28887325 | snp | C/T | | | intron-variant | MNAT1 | GRCh38.p7 | 14:60741594 | TCGATCTCCTGACCT[C/T]GTGATCCTCCTGCCT | 4331 |
rs33910094 | in-del | -/TG | | | intron-variant | MNAT1 | GRCh38.p7 | 14:60861574 | TTTTTAAAAAAATTT[-/TG]GAAAAGGTCTACAGG | 4331 |
rs33957783 | in-del | -/AA | 0 | 0 | intron-variant | MNAT1 | GRCh38.p7 | 14:60762724 | AAAAAAAAAAAAAAA[-/AA]GACATTGTGTGGTAA | 4331 |
rs33970682 | in-del | -/T/TT/TTT | 0 | 0 | intron-variant | MNAT1 | GRCh38.p7 | 14:60951266 | CAGGCTTCCCCTCCC[-/T/TT/TTT]TTTTTTTTTTTTTTT | 4331 |
rs34011061 | in-del | -/C | | | intron-variant | MNAT1 | GRCh38.p7 | 14:60900955 | TCATGTCACTGTACT[-/C]CCAGCCTGGGTGACC | 4331 |
rs34019232 | in-del | -/G | | | intron-variant | MNAT1 | GRCh38.p7 | 14:60809417 | AAAAGTATCTTATTT[-/G]CTGAGAGCATCAGTA | 4331 |
rs34046921 | in-del | -/A | | | intron-variant | MNAT1 | GRCh38.p7 | 14:60917018 | TAAGCATTGGCTTTT[-/A]AAAACTTTTGTAAAA | 4331 |
rs34133616 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | MNAT1 | GRCh38.p7 | 14:60738858 | GCTCTTAATGAAAAA[A/T]TTTTTGATAGTTTGT | 4331 |
rs34204662 | in-del | -/C | | | intron-variant | MNAT1 | GRCh38.p7 | 14:60827384 | CCTTTTCTGAGTGCA[-/C]ACAGATAGTATTTAG | 4331 |
rs34245073 | in-del | -/A | | | intron-variant | MNAT1 | GRCh38.p7 | 14:60812359 | GTGGGTTAGGAATTT[-/A]AAGTGGTTCTTTTGG | 4331 |
rs34279143 | snp | C/T | 0.031825 | 0.122064 | intron-variant | MNAT1 | GRCh38.p7 | 14:60827605 | CCAAAGAACAAAAAA[C/T]AAAACTTGACCAGGT | 4331 |
rs34304582 | in-del | -/G | | | intron-variant | MNAT1 | GRCh38.p7 | 14:60895689 | TAATCCTAGCACTTT[-/G]GGGAGGCTGAGTTGG | 4331 |
rs34357276 | in-del | -/G | | | intron-variant | MNAT1 | GRCh38.p7 | 14:60792155 | ATTTTTTTCATGTGT[-/G]TTTCCATGAATCCTT | 4331 |
rs34374326 | in-del | -/A | | | intron-variant | MNAT1 | GRCh38.p7 | 14:60876420 | TAAAAAAATTGTGGT[-/A]AAAATACATGTAACA | 4331 |
rs34411319 | in-del | -/T | | | intron-variant | MNAT1 | GRCh38.p7 | 14:60830756 | ATAATTCCTATACAA[-/T]TTTTTATTGCTATTT | 4331 |
rs34467836 | in-del | -/A | | | intron-variant | MNAT1 | GRCh38.p7 | 14:60886897 | ATAATACTTCCAATT[-/A]CTATGTTGAATGTAA | 4331 |
rs34469314 | in-del | -/C | | | intron-variant | MNAT1 | GRCh38.p7 | 14:60879581 | CTGCAATGCATTGTA[-/C]CCCATGGAACAGCAC | 4331 |
rs34495842 | in-del | -/A | | | intron-variant | MNAT1 | GRCh38.p7 | 14:60907271 | AACCTCGTTTCTACT[-/A]AAAATACAAAAATTA | 4331 |
rs34500213 | in-del | -/C | | | intron-variant | MNAT1 | GRCh38.p7 | 14:60892691 | CTATATAACTGTTTT[-/C]CTTTGTGTTTATTTT | 4331 |
rs34550432 | in-del | -/T | | | intron-variant | MNAT1 | GRCh38.p7 | 14:60794954 | AGGCACTGCGGATAG[-/T]AGAACAAGATAGGCA | 4331 |
rs34590363 | in-del | -/TTTTT | | | intron-variant | MNAT1 | GRCh38.p7 | 14:60741676 | TTTTTTTTTTTTTTT[-/TTTTT]TTTTAATTTTTAGTA | 4331 |
rs34590816 | in-del | -/G | | | intron-variant | MNAT1 | GRCh38.p7 | 14:60751723 | TTATCAGAAATGTTT[-/G]GGAGTGTTAGGTTTT | 4331 |
rs34683738 | in-del | -/C | | | intron-variant | MNAT1 | GRCh38.p7 | 14:60794243 | CCTCTAACCACAAAG[-/C]AATAGTGAAAATGCA | 4331 |
rs34732694 | snp | A/C | 0.5 | 0 | intron-variant | MNAT1 | GRCh38.p7 | 14:60748833 | AACAATTAAGAAGTC[A/C]CAGTATCGTAAATGC | 4331 |
rs34732949 | in-del | -/A | | | intron-variant | MNAT1 | GRCh38.p7 | 14:60876373 | TAATTCTAGCAAAGC[-/A]AAATGAGGAAATTAG | 4331 |
rs34733132 | in-del | -/C | | | intron-variant | MNAT1 | GRCh38.p7 | 14:60746448 | GAACCTGGGAGGTGG[-/C]AGGTTGCAGTGAGCC | 4331 |
rs34771041 | in-del | -/AA | | | intron-variant | MNAT1 | GRCh38.p7 | 14:60942003 | ATGAGGCTCCATCTC[-/AA]AAAAAAAAAAAAAAA | 4331 |
rs34782703 | in-del | -/C | | | intron-variant | MNAT1 | GRCh38.p7 | 14:60934112 | TCAGAAGTTCAAAGT[-/C]CCAAGTTGTTGACAA | 4331 |
rs34787165 | in-del | -/C | | | intron-variant | MNAT1 | GRCh38.p7 | 14:60872065 | TGCTATGAAGGAATA[-/C]CCTGAGACTGGATAA | 4331 |
rs34806566 | in-del | -/A | | | intron-variant | MNAT1 | GRCh38.p7 | 14:60751766 | TAAGTTGGAATATGT[-/A]AAAAAAAAAAGAATT | 4331 |
rs34808051 | in-del | -/C | | | intron-variant | MNAT1 | GRCh38.p7 | 14:60779922 | CGCTGTGGTTGCTGT[-/C]CCGTGTAGTGAAAGC | 4331 |
rs34819695 | in-del | -/G | | | intron-variant | MNAT1 | GRCh38.p7 | 14:60736384 | GCACTTAGCCATTCA[-/G]GGGAAGATTATACGA | 4331 |
rs34891517 | in-del | -/C | | | intron-variant | MNAT1 | GRCh38.p7 | 14:60773650 | ATGTAAGAGAAACTG[-/C]CCCCATTCAGAAAGT | 4331 |
rs34901471 | in-del | -/T | 0.00398564 | 0.0444627 | intron-variant | MNAT1 | GRCh38.p7 | 14:60918608 | TCAACTAAATTATGG[-/T]TGCACAAACATCATA | 4331 |
rs34903139 | in-del | -/C | | | intron-variant | MNAT1 | GRCh38.p7 | 14:60965533 | GCTGTATGCACACTG[-/C]CAAGTTTATGCTCAA | 4331 |
rs34974330 | in-del | -/C | | | intron-variant | MNAT1 | GRCh38.p7 | 14:60961403 | GCTGAAACCACCTGT[-/C]CCCCTATATTCTCAA | 4331 |
rs35012398 | in-del | -/A | 0.321644 | 0.239514 | intron-variant | MNAT1 | GRCh38.p7 | 14:60800197 | TGTGTAAGGTTGGGG[-/A]AAAAATTGTAAAACT | 4331 |
rs35013411 | in-del | -/G | | | intron-variant | MNAT1 | GRCh38.p7 | 14:60782240 | ACATGTTGAGCTTAT[-/G]GGGGGACCATTTGAG | 4331 |
rs35026786 | in-del | -/ACA | 0.0107246 | 0.0724382 | intron-variant | MNAT1 | GRCh38.p7 | 14:60966418 | CGCCACCACACCCAG[-/ACA]ACAATGACTAATTAA | 4331 |
rs35029197 | in-del | -/T | | | intron-variant | MNAT1 | GRCh38.p7 | 14:60825584 | AATAAGTATTACTTT[-/T]CTGTTTTTATATCTT | 4331 |
rs35038333 | in-del | -/A | | | intron-variant | MNAT1 | GRCh38.p7 | 14:60893479 | TTTAGTTATTATTTG[-/A]AATATTGGACATTCT | 4331 |
rs35048266 | snp | C/T | | | intron-variant | MNAT1 | GRCh38.p7 | 14:60854293 | CCAGCTTCTGAAGCC[C/T]ACTTCTGTCAGTTCA | 4331 |
rs35086294 | in-del | -/C | | | intron-variant | MNAT1 | GRCh38.p7 | 14:60887072 | TGTTATGAAAAGATT[-/C]TTGAACTTTGTCAAA | 4331 |
rs35137765 | in-del | -/G | | | intron-variant | MNAT1 | GRCh38.p7 | 14:60788838 | TAGGTTTTGGTTTAA[-/G]GGGAATGTTGTGGCT | 4331 |
rs35144046 | in-del | -/A | | | intron-variant | MNAT1 | GRCh38.p7 | 14:60965600 | GAAGCAAGCTGTACC[-/A]AAAATGTGATGAATC | 4331 |
rs35176907 | in-del | -/C | | | intron-variant | MNAT1 | GRCh38.p7 | 14:60820988 | GAGCAGTAAAGAAGG[-/C]CTAAGGTAAGAAACA | 4331 |
rs35183266 | snp | A/T | 0.0322114 | 0.122752 | intron-variant | MNAT1 | GRCh38.p7 | 14:60949806 | TTTTTTCTAAAGTGA[A/T]GTTTTTTCCAAAGTG | 4331 |
rs35188899 | snp | A/C | 0.126004 | 0.217083 | missense, intron-variant | MNAT1 | GRCh38.p7 | 14:60968264 | CTGCCTCACCACAGG[A/C]CCTTGCTGGAGGCTA | 4331 |
rs35218347 | in-del | -/A | | | intron-variant | MNAT1 | GRCh38.p7 | 14:60762976 | TCATGTATGGACTTT[-/A]AAAGCCAAAAGGAAC | 4331 |
rs35252891 | in-del | -/C | | | intron-variant | MNAT1 | GRCh38.p7 | 14:60946074 | CCCACCACCTGTGTT[-/C]CCATGGCCTACTTTT | 4331 |
rs35253003 | in-del | -/T | | | intron-variant | MNAT1 | GRCh38.p7 | 14:60842993 | TCAAAAACTTGTAAG[-/T]TCAAACCGTCATAAG | 4331 |
rs35258950 | in-del | -/C | | | intron-variant | MNAT1 | GRCh38.p7 | 14:60828726 | GAAAGCTCCAGGTGG[-/C]TAACCTGTACTGTTG | 4331 |
rs35286965 | in-del | -/G | | | intron-variant | MNAT1 | GRCh38.p7 | 14:60916320 | ACATTTTTAAAAATA[-/G]GAATAAAATAAAAAG | 4331 |
rs35304386 | snp | C/T | 0.470132 | 0.118498 | intron-variant | MNAT1 | GRCh38.p7 | 14:60887277 | AAGTTTTAGGGTACA[C/T]GTGCACAATGTGCAG | 4331 |
rs35305776 | in-del | -/C | | | intron-variant | MNAT1 | GRCh38.p7 | 14:60954082 | GTTTTTATGCCAGTA[-/C]CCAGGCTGTTTTGAT | 4331 |
rs35394484 | in-del | -/C | | | intron-variant | MNAT1 | GRCh38.p7 | 14:60845225 | TGTTTCTATAGGGTT[-/C]CAGTAGTGAAACCAT | 4331 |
rs35475111 | in-del | -/A | | | intron-variant | MNAT1 | GRCh38.p7 | 14:60818674 | AGTCTTGTTGTTTTT[-/A]AGTTTTCCCTTTTTA | 4331 |
rs35508449 | in-del | -/A | | | intron-variant | MNAT1 | GRCh38.p7 | 14:60885688 | TATAGTTTGTATAGT[-/A]TTGCAAATATATTTT | 4331 |
rs35561570 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | MNAT1 | GRCh38.p7 | 14:60806031 | TGCTCCAGATCTGCA[C/T]CAGCATTTTATGTTG | 4331 |
rs35569973 | snp | G/T | | | intron-variant | MNAT1 | GRCh38.p7 | 14:60820713 | TAACATTCCACCTGG[G/T]GTCTCTATTCATCTG | 4331 |
rs35593777 | in-del | -/G | | | intron-variant | MNAT1 | GRCh38.p7 | 14:60807026 | TTATGTTAAAAAACT[-/G]GGAGAAGTTGCTAGA | 4331 |
rs35645256 | in-del | -/T | 0.226188 | 0.248863 | intron-variant | MNAT1 | GRCh38.p7 | 14:60831104 | GCTTTCTTTTGTTCC[-/T]TTTTTTTTTTTTTCA | 4331 |
rs35712843 | in-del | -/T | 0.332337 | 0.236052 | intron-variant | MNAT1 | GRCh38.p7 | 14:60943617 | AAGGATTTGTTTCTC[-/T]TTTTTTTTTTAATTC | 4331 |
rs35719600 | snp | A/T | 0.0475351 | 0.146656 | intron-variant | MNAT1 | GRCh38.p7 | 14:60911030 | CTATTCAGAGATTCA[A/T]CTTCTTCCTGGTTTA | 4331 |
rs35766148 | in-del | -/T | | | intron-variant | MNAT1 | GRCh38.p7 | 14:60960900 | CTTGCTTTTCTCTAA[-/T]TCCATTGGGCAGCCA | 4331 |
rs35825181 | in-del | -/T | 0 | 0 | intron-variant | MNAT1 | GRCh38.p7 | 14:60903866 | TTTTTTTTTTTTTTT[-/T]CTTTTTGATGGAGTT | 4331 |
rs35831995 | in-del | -/G | | | intron-variant | MNAT1 | GRCh38.p7 | 14:60827979 | TATTTTAAAGAAAAT[-/G]GGAGGTTCTTAAAAC | 4331 |
rs35860926 | in-del | -/C | | | intron-variant | MNAT1 | GRCh38.p7 | 14:60936213 | GAGATTCTCCGGAGA[-/C]CCCTTTTTTGTGTGT | 4331 |
rs35882600 | in-del | -/C | | | intron-variant | MNAT1 | GRCh38.p7 | 14:60894695 | TGTTTGTGTGTGTGT[-/C]CTGTTGGTGGTGGTG | 4331 |
rs35919903 | in-del | -/C | | | intron-variant | MNAT1 | GRCh38.p7 | 14:60907545 | GTTCCTAGAATCAGG[-/C]CTAAGCGGGCAGATC | 4331 |
rs35941535 | in-del | -/C | | | intron-variant | MNAT1 | GRCh38.p7 | 14:60865174 | GGCGTAAAGAAACTT[-/C]CTATCTTTTCACGGA | 4331 |
rs35945471 | in-del | -/TTCC | | | intron-variant | MNAT1 | GRCh38.p7 | 14:60834925 | CATTATGTAGTGCCC[-/TTCC]TTCCTTCCTTCCTTC | 4331 |
rs36011351 | in-del | -/G | | | intron-variant | MNAT1 | GRCh38.p7 | 14:60880837 | AGCATGAAGCCAACA[-/G]GGATGTAAAACAACC | 4331 |
rs36036475 | in-del | -/T | | | intron-variant | MNAT1 | GRCh38.p7 | 14:60855773 | GCCCCTCCCCCCAAC[-/T]TTTTTTATTATTATC | 4331 |
rs36040227 | snp | C/T | | | intron-variant | MNAT1 | GRCh38.p7 | 14:60854296 | GCTTCTGAAGCCTAC[C/T]TCTGTCAGTTCATCA | 4331 |
rs36080643 | in-del | -/C | | | intron-variant | MNAT1 | GRCh38.p7 | 14:60870082 | TTATTAAAAATACTG[-/C]CCATGTATAACTACC | 4331 |
rs36100303 | in-del | -/G | | | intron-variant | MNAT1 | GRCh38.p7 | 14:60808821 | ACAGACGGTGATGGA[-/G]GCTACCAAGAGGGAG | 4331 |
rs56107429 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | MNAT1 | GRCh38.p7 | 14:60896224 | ACAATACATAAACAT[A/G]TTTTATTCTGTGCCA | 4331 |
rs56232128 | in-del | -/G | 0.494358 | 0.0528145 | intron-variant | MNAT1 | GRCh38.p7 | 14:60776941 | CAGCCTTGACTTCCC[-/G]GGCTCAGGTGTTTCT | 4331 |
rs56243570 | snp | C/G | 0.301429 | 0.244653 | intron-variant | MNAT1 | GRCh38.p7 | 14:60917289 | ATTTTCAGTTTCTAA[C/G]CCTCATTTTACCAGG | 4331 |
rs56252694 | snp | A/G | 0.291493 | 0.246533 | intron-variant | MNAT1 | GRCh38.p7 | 14:60938656 | TTTTTGAGAATTTTT[A/G]TATCAATGTTCATCA | 4331 |
rs56345746 | in-del | -/A | 0 | 0 | intron-variant | MNAT1 | GRCh38.p7 | 14:60901043 | AAAAAAAAAAAAAAA[-/A]GTCAATGCCTGTTTC | 4331 |
rs56397090 | snp | G/T | | | upstream-variant-2KB | MNAT1 | GRCh38.p7 | 14:60734553 | TGTGACACAGTACCT[G/T]GAAAAATGCAACTGG | 4331 |
rs56662776 | snp | A/G | 0.0322114 | 0.122752 | intron-variant | MNAT1 | GRCh38.p7 | 14:60871807 | TTTTTATTTTTAGTA[A/G]AGATGGGGTTTCACC | 4331 |
rs56775018 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | MNAT1 | GRCh38.p7 | 14:60846229 | AGAAATTGGTCAGTT[C/T]CTTCTAAGTTGAATT | 4331 |
rs57005757 | snp | C/T | | | intron-variant | MNAT1 | GRCh38.p7 | 14:60961579 | TTCATGTTGGCTTCT[C/T]TTTTTATCCACATTC | 4331 |
rs57127110 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | MNAT1 | GRCh38.p7 | 14:60736753 | CCGTTCTTCTTGTTG[C/G]TACAATAGAGAAAAT | 4331 |
rs57138643 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MNAT1 | GRCh38.p7 | 14:60912647 | GAATGTTGAATATTG[A/G]CCCCCACTGTCTTCT | 4331 |
rs57237709 | snp | G/T | | | intron-variant | MNAT1 | GRCh38.p7 | 14:60780951 | AAGTAGCTTGACTCA[G/T]TATAGGTAGGGAGAT | 4331 |
rs57312807 | snp | C/T | | | intron-variant | MNAT1 | GRCh38.p7 | 14:60846814 | ACTTGAAATTTTATT[C/T]TATATTTGGGAAGAA | 4331 |
rs57354716 | in-del | -/T | | | intron-variant | MNAT1 | GRCh38.p7 | 14:60929170 | AAAAAAAAAAAAAAA[-/T]ATATATATATATATA | 4331 |
rs57467549 | in-del | -/T | 0.0193772 | 0.0965046 | intron-variant | MNAT1 | GRCh38.p7 | 14:60764478 | AATGGGCTATTTGGG[-/T]TTGGAACCCATACTT | 4331 |
rs57733236 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | MNAT1 | GRCh38.p7 | 14:60914154 | ATCTCCTGGTGTGCC[A/G]TTTGTTAAGCCTGTT | 4331 |
rs57830544 | in-del | -/T | | | intron-variant | MNAT1 | GRCh38.p7 | 14:60929169 | AAAAAAAAAAAAAAA[-/T]AATATATATATATAT | 4331 |
rs57837834 | in-del | -/T | | | intron-variant | MNAT1 | GRCh38.p7 | 14:60929168 | AAAAAAAAAAAAAAA[-/T]AAATATATATATATA | 4331 |
rs57914358 | snp | C/T | | | intron-variant | MNAT1 | GRCh38.p7 | 14:60941701 | AGTTAGACCCTGTTT[C/T]TTAAAAAAAAAAAAA | 4331 |
rs57943366 | snp | A/C | | | intron-variant | MNAT1 | GRCh38.p7 | 14:60745080 | CAACTACCCTGCATT[A/C]TGATCTCTGCCTATT | 4331 |
rs57979441 | snp | A/T | | | intron-variant | MNAT1 | GRCh38.p7 | 14:60929164 | AAAAAAAAAAAAAAA[A/T]AAAAAAATATATATA | 4331 |
rs58073559 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | MNAT1 | GRCh38.p7 | 14:60913563 | CAGGACCCTCAGCTG[C/T]AGGTCTGTTGGAGTT | 4331 |
rs58076734 | in-del | -/ATT | 0 | 0 | intron-variant | MNAT1 | GRCh38.p7 | 14:60899956 | GCTGTTACTATTATT[-/ATT]GTTTTGGTTGCCACA | 4331 |
rs58230510 | snp | C/G | 0.0119091 | 0.0762411 | intron-variant | MNAT1 | GRCh38.p7 | 14:60964196 | CACAAGAAAATGACA[C/G]TGTAGGAAACCAAAG | 4331 |
rs58286115 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | MNAT1 | GRCh38.p7 | 14:60852904 | TGTTCCATTGGTCTA[C/T]ATATCTGTTTTGTTA | 4331 |
rs58724794 | snp | A/G | | | intron-variant | MNAT1 | GRCh38.p7 | 14:60918229 | TTTTTTTTTTTTTGA[A/G]ATGGAGTCTCGGTCT | 4331 |
rs58782617 | snp | C/T | | | intron-variant | MNAT1 | GRCh38.p7 | 14:60814432 | TCTTTTTGCATTCTT[C/T]TCTTTCCCTTTATGT | 4331 |
rs58874872 | in-del | -/T | 0.308166 | 0.243139 | intron-variant | MNAT1 | GRCh38.p7 | 14:60866308 | GGGGTTATTTTGACC[-/T]TTTTTTTTTTTTTTT | 4331 |
rs59179458 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | MNAT1 | GRCh38.p7 | 14:60834371 | GTGTCTTTGTTCTCA[C/T]TGGTTCAAAGAACTT | 4331 |
rs59229360 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | MNAT1 | GRCh38.p7 | 14:60921780 | TAACTGGTTTTAAAT[A/G]TAAAAACATAAATCC | 4331 |
rs59405493 | snp | A/C | | | intron-variant | MNAT1 | GRCh38.p7 | 14:60814390 | TTGATGACTTCACAA[A/C]CCGGAAAATCTTCCT | 4331 |
rs59608855 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | MNAT1 | GRCh38.p7 | 14:60774724 | TGTAGAGTCATCAGT[C/T]TTGGTATTAATTAGA | 4331 |
rs59649409 | in-del | -/C | | | intron-variant | MNAT1 | GRCh38.p7 | 14:60927542 | TTCACAAGGGTGCCC[-/C]TGTACTTGGAGTTTA | 4331 |
rs59690386 | snp | C/T | | | intron-variant | MNAT1 | GRCh38.p7 | 14:60766498 | GCCGGTGGATCATGA[C/T]GTCAGGAGATCGAGA | 4331 |
rs59806218 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | MNAT1 | GRCh38.p7 | 14:60834562 | TTGCATTTGCTGAGG[A/C]GTGTTTAACTTCCAA | 4331 |
rs59923470 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MNAT1 | GRCh38.p7 | 14:60771425 | ACGAATTTATGGTAG[C/T]GGCTCATACATTAGT | 4331 |
rs60175838 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | MNAT1 | GRCh38.p7 | 14:60862567 | AGTAAAGTGCACAAC[G/T]GCTTTTGTAGAGGTC | 4331 |
rs60261472 | in-del | -/TGTGTGCG | 0 | 0 | intron-variant | MNAT1 | GRCh38.p7 | 14:60898136 | GTGTGTGTGTGTGTG[-/TGTGTGCG]CGCGCCACATTTTTT | 4331 |
rs60866925 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | MNAT1 | GRCh38.p7 | 14:60738898 | ATGGCATATATTTCA[C/T]GGGATTGAATATAGG | 4331 |
rs60961683 | snp | G/T | 0.0267878 | 0.112589 | intron-variant | MNAT1 | GRCh38.p7 | 14:60767404 | CATCTGGGATCTTTT[G/T]TGGATACTCTACACT | 4331 |
rs60969481 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | MNAT1 | GRCh38.p7 | 14:60942755 | ATTTTAGAAATTAAA[A/G]TTAAAGCTTCTTTAA | 4331 |
rs61077085 | in-del | -/T | 0.459004 | 0.137176 | intron-variant | MNAT1 | GRCh38.p7 | 14:60767767 | CACCACACTTGGCTA[-/T]TTTTTTTGTTTGTTT | 4331 |
rs61149455 | in-del | -/CTCT/CTCTCTC | 0 | 0 | intron-variant | MNAT1 | GRCh38.p7 | 14:60900083 | TCTCTCTCTCTCTCT[-/CTCT/CTCTCTC]TACCTTGGACTTCCC | 4331 |
rs61211217 | snp | A/T | 0.306182 | 0.243605 | intron-variant | MNAT1 | GRCh38.p7 | 14:60909240 | CCTTTGTCAGATGAG[A/T]AGGTTGCAAAAATTT | 4331 |
rs61229600 | in-del | -/GA/T/TG/TGA | | | intron-variant | MNAT1 | GRCh38.p7 | 14:60781973 | GTGTGTGTGTGTGTG[-/GA/T/TG/TGA]ATTTTTTTTTTTTTT | 4331 |
rs61263155 | snp | C/T | 0.391954 | 0.205789 | intron-variant | MNAT1 | GRCh38.p7 | 14:60889857 | ATGAAAAAATGCTCA[C/T]CATCACTGGTCATCA | 4331 |
rs61278549 | in-del | -/CACA | | | intron-variant | MNAT1 | GRCh38.p7 | 14:60746975 | ACACACACACACACA[-/CACA]AAATTATGTCTTTTT | 4331 |
rs61300714 | in-del | -/T | 0.349013 | 0.229557 | intron-variant | MNAT1 | GRCh38.p7 | 14:60872673 | GTAAATACATAGCCA[-/T]TTTTTTTTTCAAAAC | 4331 |
rs61327947 | in-del | -/A | | | intron-variant | MNAT1 | GRCh38.p7 | 14:60772609 | CAAAAAAAAAAAAAA[-/A]GCCAATTCTTGGCTT | 4331 |
rs61423733 | in-del | -/TAT | 0 | 0 | intron-variant | MNAT1 | GRCh38.p7 | 14:60844140 | GTTTCAATAACTTAT[-/TAT]CTTGATTACTATAGT | 4331 |
rs61484165 | in-del | -/T | | | intron-variant | MNAT1 | GRCh38.p7 | 14:60949796 | AGATTATTTTTTTTT[-/T]CTAAAGTGATGTTTT | 4331 |
rs61990960 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | MNAT1 | GRCh38.p7 | 14:60922185 | AACTTGTCAGAAGCA[A/G]GTTTTGGTTAATAGA | 4331 |
rs61990961 | snp | C/T | | | intron-variant | MNAT1 | GRCh38.p7 | 14:60924064 | GAGGCAGAAGAAGTT[C/T]AAAAAGTAAAACAAA | 4331 |
rs61990962 | snp | C/G | 0.259397 | 0.249823 | intron-variant | MNAT1 | GRCh38.p7 | 14:60937679 | GATGCCTCCAGCTTT[C/G]TTCTTTTGGCTTAGG | 4331 |
rs61991696 | snp | A/G | 0.0558544 | 0.157504 | intron-variant | MNAT1 | GRCh38.p7 | 14:60749793 | CTGAGACAGCAAATA[A/G]AATGAGAATAATTGA | 4331 |
rs61991697 | snp | C/T | 0.5 | 0 | intron-variant | MNAT1 | GRCh38.p7 | 14:60757585 | TCCTAGAATATCATT[C/T]ATGTTACTCCTAGTT | 4331 |
rs61991702 | snp | A/T | 0.5 | 0 | intron-variant | MNAT1 | GRCh38.p7 | 14:60769663 | ATTAAAAAAAAAATT[A/T]GTTTTTTTTAGAGAC | 4331 |
rs61991703 | snp | A/G | 0.0569829 | 0.158885 | intron-variant | MNAT1 | GRCh38.p7 | 14:60772469 | AGGTGCCTGTACTCT[A/G]CTACTGTAATCAGCT | 4331 |
rs61991704 | snp | A/G | 0.234982 | 0.249549 | intron-variant | MNAT1 | GRCh38.p7 | 14:60788212 | TTGCACATATCCATC[A/G]GAGGTCTTAGGTGAC | 4331 |
rs61991705 | snp | G/T | 0.470811 | 0.117228 | intron-variant | MNAT1 | GRCh38.p7 | 14:60800975 | GGGGAGATAATTATG[G/T]TAACTAATAACTATA | 4331 |
rs61991706 | snp | C/T | 0.318415 | 0.240457 | intron-variant | MNAT1 | GRCh38.p7 | 14:60811069 | ATATGTTGATCCTTT[C/T]ATCATTATATAATGT | 4331 |
rs61992966 | snp | A/C | | | intron-variant | MNAT1 | GRCh38.p7 | 14:60821608 | AATTTATGCATCGAT[A/C]AAGTGTGATTTTCAT | 4331 |
rs61992967 | snp | G/T | | | intron-variant | MNAT1 | GRCh38.p7 | 14:60823962 | AGGAGTTGAAGACCA[G/T]TGTGGCCAAGATGGT | 4331 |
rs61992969 | snp | C/T | | | intron-variant | MNAT1 | GRCh38.p7 | 14:60838056 | CTCACTTTTTTTTCC[C/T]TCTGATCAGCCTGGC | 4331 |
rs61992970 | snp | G/T | 0.0569829 | 0.158885 | intron-variant | MNAT1 | GRCh38.p7 | 14:60842314 | CATTTTCCTCTCTGG[G/T]AATCTGCCCTGCAAA | 4331 |
rs61992988 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | MNAT1 | GRCh38.p7 | 14:60866541 | AATTTGTACGAATGA[A/G]ATTATAGTCAAAACA | 4331 |
rs61992989 | snp | C/T | 0.5 | 0 | intron-variant | MNAT1 | GRCh38.p7 | 14:60881788 | TTGTGTTACAAAGAA[C/T]CCAATTATATTATTT | 4331 |
rs61992990 | snp | A/G | 0.137867 | 0.223442 | intron-variant | MNAT1 | GRCh38.p7 | 14:60882616 | CAGTGGGATTGCTGG[A/G]TCATATAGTAGCTCT | 4331 |
rs61992991 | snp | C/G | | | intron-variant | MNAT1 | GRCh38.p7 | 14:60888888 | TAGGAATCCAACTTA[C/G]AAGGGATGTGAAGGA | 4331 |
rs61992992 | snp | C/T | 0 | 0 | intron-variant | MNAT1 | GRCh38.p7 | 14:60898142 | GTGTGTGTGTGTGTG[C/T]GCGCGCCACATTTTT | 4331 |
rs61993025 | snp | A/T | 0.301429 | 0.244653 | intron-variant | MNAT1 | GRCh38.p7 | 14:60910405 | CCTGTCTTGTGCCAG[A/T]TTTCAAAGGGAATGC | 4331 |
rs61993026 | snp | A/G | 0.306431 | 0.243548 | intron-variant | MNAT1 | GRCh38.p7 | 14:60912431 | TTGATAGTCTTTACA[A/G]ATTGGCATGTTTTTG | 4331 |
rs67332094 | in-del | -/TATATA | 0 | 0 | intron-variant | MNAT1 | GRCh38.p7 | 14:60794679 | ATATATATATATATA[-/TATATA]AAATAGGTATATATA | 4331 |
rs67724383 | in-del | -/ACT/TAC | 0 | 0 | intron-variant | MNAT1 | GRCh38.p7 | 14:60959530 | TGCCATGCCAGTGAT[-/ACT/TAC]TACAAACTTGGGAGT | 4331 |
rs67991933 | in-del | -/ATAT | | | intron-variant | MNAT1 | GRCh38.p7 | 14:60794669 | AAAAAAATATATATA[-/ATAT]TATATATATAAAATA | 4331 |
rs68028483 | in-del | -/A | 0.448323 | 0.15221 | intron-variant | MNAT1 | GRCh38.p7 | 14:60924384 | ATTCAGTGCCTGTTT[-/A]AAAAAAAAAAAAAAA | 4331 |
rs68107318 | in-del | -/T | | | intron-variant | MNAT1 | GRCh38.p7 | 14:60738254 | GAAAAACATCTTGGA[-/T]TTTTTTTTTTTTTTT | 4331 |
rs71114155 | in-del | -/TTTTTTT | 0 | 0 | intron-variant | MNAT1 | GRCh38.p7 | 14:60784203 | TTTTTTTTTTTTTTT[-/TTTTTTT]AGTAGAGGCGAGGTT | 4331 |
rs71114156 | in-del | -/A | 0 | 0 | intron-variant | MNAT1 | GRCh38.p7 | 14:60794656 | AAAAAAAAAAAAAAA[-/A]TATATATATATATAT | 4331 |
rs71114158 | in-del | -/AC/CA | 0 | 0 | intron-variant | MNAT1 | GRCh38.p7 | 14:60816330 | TTCAATTTTAAAAAA[-/AC/CA]GTTTGGAAAAAGATT | 4331 |
rs71114162 | in-del | -/T | 0 | 0 | intron-variant | MNAT1 | GRCh38.p7 | 14:60869057 | TTTTTTTTTTTTTTT[-/T]GAGACGGAGTCTCGC | 4331 |
rs71114163 | in-del | -/T | 0.191775 | 0.243125 | intron-variant | MNAT1 | GRCh38.p7 | 14:60887204 | TACATATCAGAGCTG[-/T]TTTTTTTTCTTGTTT | 4331 |
rs71114166 | in-del | -/A/AA | 0.375 | 0.216506 | intron-variant | MNAT1 | GRCh38.p7 | 14:60907804 | AAAAAAAAAAAAAAA[-/A/AA]GTTGCTAGAATCAAT | 4331 |
rs71114168 | in-del | -/ATT/ATTATT | 0 | 0 | intron-variant | MNAT1 | GRCh38.p7 | 14:60930247 | ATTATTATTATTATT[-/ATT/ATTATT]TGAGTCTATTTCCTT | 4331 |
rs71114169 | in-del | -/T/TT | 0.451608 | 0.147832 | intron-variant | MNAT1 | GRCh38.p7 | 14:60942443 | TTTTTTTTTTTTTTT[-/T/TT]GTAAATTTGGACTCT | 4331 |
rs71114171 | in-del | -/TTTT | 0.2776 | 0.248472 | intron-variant | MNAT1 | GRCh38.p7 | 14:60958623 | CTTTTTCCTTCTTTC[-/TTTT]GAGACAAGGTCTTTT | 4331 |
rs71114172 | in-del | -/T | 0 | 0 | intron-variant | MNAT1 | GRCh38.p7 | 14:60958654 | TTTTTTTTTTTTTTT[-/T]GAGACAGAGTCTCGC | 4331 |
rs71114173 | in-del | -/T | 0 | 0 | intron-variant | MNAT1 | GRCh38.p7 | 14:60966602 | CTGCAACCTCCACCT[-/T]CCTGGGTTCAAGTGA | 4331 |
rs71395636 | in-del | AA/TATAT | 0.5 | 0 | intron-variant | MNAT1 | GRCh38.p7 | 14:60794657 | AAAAAAAAAAAAAAA[AA/TATAT]ATATATATATATATA | 4331 |
rs71410680 | multinucleotide-polymorphism | ATA/TTT | 0.5 | 0 | intron-variant | MNAT1 | GRCh38.p7 | 14:60869043 | TATATATATATATAT[ATA/TTT]TTTTTTTTTTTTTTG | 4331 |
rs71416075 | snp | A/C | 0.5 | 0 | intron-variant, utr-variant-5-prime | MNAT1 | GRCh38.p7 | 14:60799716 | AATATATATATATAT[A/C]CACACACACACTGCA | 4331 |
rs71416076 | snp | C/G | 0.00795532 | 0.062565 | intron-variant | MNAT1 | GRCh38.p7 | 14:60827339 | TGGGTGAGCCAGAAG[C/G]GAGCAGAGTACTCAT | 4331 |
rs71416077 | snp | G/T | 0.5 | 0 | intron-variant | MNAT1 | GRCh38.p7 | 14:60841362 | TATTTATCTTATTTG[G/T]TATGTTTTTCATTTT | 4331 |
rs71416078 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | MNAT1 | GRCh38.p7 | 14:60906782 | TGGTTTTCAAATACT[C/T]GTTTCTGAAAAAATC | 4331 |
rs71416079 | snp | G/T | 0.5 | 0 | intron-variant | MNAT1 | GRCh38.p7 | 14:60951298 | TTTTGCTGTTTTTGT[G/T]GCTACTTTGTCTTAT | 4331 |
rs71416080 | snp | G/T | 0.5 | 0 | intron-variant | MNAT1 | GRCh38.p7 | 14:60962985 | GCCATATGTTTTTTG[G/T]TTTTTGTTTTTTTTA | 4331 |
rs71449539 | in-del | -/A | 0.5 | 0 | intron-variant | MNAT1 | GRCh38.p7 | 14:60794637 | CTTCACTGCATTCTC[-/A]AAAAAAAAAAAAAAA | 4331 |
rs71449540 | in-del | -/C | 0.5 | 0 | intron-variant | MNAT1 | GRCh38.p7 | 14:60823824 | GATTGTGCCACTGCA[-/C]CCCTAGCCTGGGCAA | 4331 |
rs71449542 | in-del | -/ATT/TTATTA/TTATTATTA | 0.5 | 0 | intron-variant | MNAT1 | GRCh38.p7 | 14:60930206 | TCTTCTTCCGTCTTT[-/ATT/TTATTA/TTATTATTA]ATTATTATTATTATT | 4331 |
rs72148606 | in-del | -/TAT | 0.0486741 | 0.148216 | intron-variant | MNAT1 | GRCh38.p7 | 14:60800155 | TAAATACATATTTAA[-/TAT]TATATGTAATTTAAA | 4331 |
rs72722239 | snp | G/T | 0.00953873 | 0.0683987 | intron-variant | MNAT1 | GRCh38.p7 | 14:60748369 | CTGAATAGCTGCGAC[G/T]CCAGGTTGGCGCCAC | 4331 |
rs72722241 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | MNAT1 | GRCh38.p7 | 14:60755941 | GAGAGGCTGGGGAAA[A/T]GGGACCGCTTTCTAA | 4331 |
rs72722247 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | MNAT1 | GRCh38.p7 | 14:60778630 | TCTCTTACCAAGAGT[C/T]GCACTTTACAGGAAA | 4331 |
rs72722248 | snp | C/T | 0.0275645 | 0.114116 | intron-variant | MNAT1 | GRCh38.p7 | 14:60779216 | CGCTGATATGTCTCA[C/T]GGTGTTCCTAAGCCC | 4331 |
rs72722250 | snp | A/G | | | intron-variant | MNAT1 | GRCh38.p7 | 14:60786134 | AGAAATTAGTAAATT[A/G]GAAAACACACAAAAA | 4331 |
rs72722257 | snp | C/T | 0.0271762 | 0.113356 | intron-variant | MNAT1 | GRCh38.p7 | 14:60795274 | AAGGAACTGCTCTCT[C/T]CTCCCATCCATCTTT | 4331 |
rs72722263 | snp | A/G | | | intron-variant | MNAT1 | GRCh38.p7 | 14:60810775 | CCTAACTTGTGACCT[A/G]TCCTGTAGAAAGTTC | 4331 |
rs72722266 | snp | A/G | 0.0322114 | 0.122752 | intron-variant | MNAT1 | GRCh38.p7 | 14:60813344 | TCCCTCCCACATAGA[A/G]TTGAGTGCAGTGGGT | 4331 |
rs72722268 | snp | A/C | | | intron-variant | MNAT1 | GRCh38.p7 | 14:60825029 | AGAGTGGGAAAAAAA[A/C]AAGCCACAAAGTGAC | 4331 |
rs72722269 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MNAT1 | GRCh38.p7 | 14:60825149 | GCATTTCTAAAAATA[A/G]GATAGCCAATCCTCA | 4331 |
rs72722273 | snp | C/G | 0.0670745 | 0.170406 | intron-variant | MNAT1 | GRCh38.p7 | 14:60830393 | TTTTTACTAGTTAGT[C/G]ATCTGTTGAATAAGT | 4331 |
rs72722276 | snp | C/T | 0.262985 | 0.249663 | intron-variant | MNAT1 | GRCh38.p7 | 14:60845696 | CTTCTGCTTTCACTC[C/T]GAGCCCTAGGCAACC | 4331 |
rs72722280 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | MNAT1 | GRCh38.p7 | 14:60861269 | TGTTTTAGTAATAAA[C/T]GTAAAAACGTTCAAA | 4331 |
rs72722284 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | MNAT1 | GRCh38.p7 | 14:60871220 | ATTGTTTCCACTATT[C/T]GGCTGCTATTAATAG | 4331 |
rs72722285 | snp | C/T | | | intron-variant | MNAT1 | GRCh38.p7 | 14:60875843 | TCCTTAAGTATTATC[C/T]TCCTTGGAAGGTAAT | 4331 |
rs72722286 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | MNAT1 | GRCh38.p7 | 14:60876900 | TAAATATGCATTGGT[A/G]TACAAATATTTCTTT | 4331 |
rs72722300 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | MNAT1 | GRCh38.p7 | 14:60920195 | GGGACCAGCAGAGCC[C/T]AAGCCCACCAATAGA | 4331 |
rs73311456 | snp | G/T | 0.5 | 0 | intron-variant | MNAT1 | GRCh38.p7 | 14:60752392 | TATTTTAAAATAGAT[G/T]TATTTTAAGCATGTC | 4331 |
rs73311467 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MNAT1 | GRCh38.p7 | 14:60839768 | ACTTGCGGTGCATCT[A/G]ATCCAGCCTCAGGCT | 4331 |
rs73311473 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | MNAT1 | GRCh38.p7 | 14:60863526 | GCTCCAAAGCTGTTT[G/T]ACTAAACTCTCTCAT | 4331 |
rs73311477 | snp | A/G | 0.0517044 | 0.152246 | intron-variant | MNAT1 | GRCh38.p7 | 14:60872233 | AACCAGCTCTCACGT[A/G]AACTAATAGAGAATT | 4331 |
rs73311489 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | MNAT1 | GRCh38.p7 | 14:60952840 | CAGAGACAGAATCAA[G/T]AATCAGGAAAGAGAG | 4331 |
rs74053494 | snp | G/T | 0.0422008 | 0.138995 | intron-variant | MNAT1 | GRCh38.p7 | 14:60744605 | TTGCAGGTAGTTCAG[G/T]TACTGGCAGATAACT | 4331 |
rs74053496 | snp | A/T | 0.5 | 0 | intron-variant | MNAT1 | GRCh38.p7 | 14:60758881 | TGTTAGTATTAAAAC[A/T]AAAAGTATATGCCTT | 4331 |
rs74053827 | snp | C/T | 0.0539704 | 0.155153 | intron-variant | MNAT1 | GRCh38.p7 | 14:60841800 | TAGCATGTACAAGAA[C/T]AGATTTTAATGTTAG | 4331 |
rs74053889 | snp | C/T | 0.0513262 | 0.151752 | intron-variant | MNAT1 | GRCh38.p7 | 14:60920010 | AGATGACAAAGGTAT[C/T]CTAGTACTGTGAGCA | 4331 |
rs74053899 | snp | G/T | 0.0329836 | 0.124112 | intron-variant | MNAT1 | GRCh38.p7 | 14:60942216 | GTCTTAAAGAGTTCA[G/T]CCAAAAAGCACATCT | 4331 |
rs74053900 | snp | G/T | 0.5 | 0 | intron-variant | MNAT1 | GRCh38.p7 | 14:60942459 | TTTTTTTTTTTTTTT[G/T]TAAATTTGGACTCTT | 4331 |
rs74310287 | in-del | -/TAT | | | intron-variant | MNAT1 | GRCh38.p7 | 14:60844139 | TGTTTCAATAACTTA[-/TAT]TCTTGATTACTATAG | 4331 |
rs74385027 | snp | C/T | 0.0633504 | 0.166319 | intron-variant | MNAT1 | GRCh38.p7 | 14:60779514 | CTGTTTCCGGCTGGG[C/T]GCGGTGGCCCACACC | 4331 |
rs74427212 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant, upstream-variant-2KB | MNAT1 | GRCh38.p7 | 14:60789783 | TGGCTACAGAATAGT[C/T]CACATATTTCAGAAA | 4331 |
rs74433085 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant, upstream-variant-2KB | MNAT1 | GRCh38.p7 | 14:60799110 | AACTGTTACCTGAAA[C/T]TTTTCTCATATGTCT | 4331 |
rs74435139 | snp | C/T | 0.5 | 0 | intron-variant | MNAT1 | GRCh38.p7 | 14:60958623 | TCTTTTTCCTTCTTT[C/T]GAGACAAGGTCTTTT | 4331 |
rs74480628 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | MNAT1 | GRCh38.p7 | 14:60934781 | ATCTCTTCTGTCTTT[C/T]TCCTTCCTCTCTTTC | 4331 |
rs74512997 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | MNAT1 | GRCh38.p7 | 14:60885850 | GCCAAAGTTAACATC[A/G]AGGATCTTTCTCACT | 4331 |
rs74563663 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MNAT1 | GRCh38.p7 | 14:60825417 | TTTAGAAAAATCAAT[C/T]CTGAATGAAGGATGA | 4331 |
rs74585755 | snp | C/G | 0.5 | 0 | intron-variant | MNAT1 | GRCh38.p7 | 14:60813731 | AGTCTCTATCCCAAT[C/G]TGAGTTTAGTGATAA | 4331 |
rs74675860 | snp | G/T | 0.0260105 | 0.111035 | intron-variant | MNAT1 | GRCh38.p7 | 14:60737229 | CGTAAGTTATTAAGT[G/T]AAAGGTAAAAATTTC | 4331 |
rs74704730 | snp | G/T | 0 | 0 | intron-variant | MNAT1 | GRCh38.p7 | 14:60959924 | TTGGTTTTTATGTTT[G/T]TTTTTTTTTTTTTGC | 4331 |
rs74720382 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | MNAT1 | GRCh38.p7 | 14:60795595 | GAATAAAGCTTTTAT[A/G]AGCAGCCACTCTTTC | 4331 |
rs74729390 | snp | C/T | 0.5 | 0 | intron-variant | MNAT1 | GRCh38.p7 | 14:60828377 | CCCAGTAAATTGTGA[C/T]TGAAGGTAGAGTTTG | 4331 |
rs74734942 | snp | A/T | 0.5 | 0 | intron-variant | MNAT1 | GRCh38.p7 | 14:60794658 | AAAAAAAAAAAAAAA[A/T]AAATATATATATATA | 4331 |
rs74821906 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | MNAT1 | GRCh38.p7 | 14:60862315 | ATGTAAAATAAATCT[A/G]AATATGCCATACGAT | 4331 |
rs74849961 | in-del | -/AA | | | intron-variant | MNAT1 | GRCh38.p7 | 14:60941715 | TCTTAAAAAAAAAAA[-/AA]GTCAATGGCCGGGCG | 4331 |
rs74873777 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | MNAT1 | GRCh38.p7 | 14:60830956 | GAATGGATACATTCC[C/T]ATTCTGTCAGTGCCG | 4331 |
rs74900334 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | MNAT1 | GRCh38.p7 | 14:60935513 | CAGATGTGTTGCTTT[A/G]TTCCTTGTCTTCAAG | 4331 |
rs74937565 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | MNAT1 | GRCh38.p7 | 14:60770461 | GTGCTGGATCATATG[A/G]TAGTTTTATTTTAAA | 4331 |
rs74951241 | snp | C/T | 0.5 | 0 | intron-variant | MNAT1 | GRCh38.p7 | 14:60737853 | GGGAAACCCTATCCT[C/T]TTTTTTTTTTTTTGA | 4331 |
rs74953273 | snp | C/T | 0.0482946 | 0.147699 | intron-variant | MNAT1 | GRCh38.p7 | 14:60747649 | GAGTGAATGTTAAGG[C/T]CTAGGATATTACTAT | 4331 |
rs74972627 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | MNAT1 | GRCh38.p7 | 14:60915183 | TTCTACTATTTACCT[C/T]TGTATTTCTAAATAA | 4331 |
rs74973137 | snp | G/T | 0.5 | 0 | intron-variant | MNAT1 | GRCh38.p7 | 14:60737865 | CCTTTTTTTTTTTTT[G/T]TGAGAAGGAGTCTCG | 4331 |
rs74975337 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | MNAT1 | GRCh38.p7 | 14:60793933 | CAATAAAAAATTTTA[A/G]TACTATTTAAATTAT | 4331 |
rs75016699 | snp | A/C | | | intron-variant | MNAT1 | GRCh38.p7 | 14:60834997 | TTGCTCCCGCCCTCC[A/C]TCCCTCCCTCCCTCT | 4331 |
rs75041426 | snp | A/G | 0.0444908 | 0.142359 | intron-variant | MNAT1 | GRCh38.p7 | 14:60756434 | ATAGAGTATGAGCTA[A/G]GAAGTGCTTTTCCCA | 4331 |
rs75050406 | snp | C/G | 0.5 | 0 | intron-variant | MNAT1 | GRCh38.p7 | 14:60766451 | TGGCGTGGTGGCTCA[C/G]GCCTGTAATCCCAGC | 4331 |
rs75070772 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | MNAT1 | GRCh38.p7 | 14:60790107 | AGTGTGTAATAGGAA[C/T]TTAGGAGAGATTTTT | 4331 |
rs75127830 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | MNAT1 | GRCh38.p7 | 14:60891225 | TTTAAGTCTTCTCTC[A/G]TTTTTTCTTAGTCTG | 4331 |
rs75131018 | snp | A/C | 0.5 | 0 | intron-variant | MNAT1 | GRCh38.p7 | 14:60766345 | GAGCGAGACTCTGTC[A/C]AAAAAAAAAAAAGAA | 4331 |
rs75151457 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MNAT1 | GRCh38.p7 | 14:60866830 | GGAAGATACTATTTC[C/T]TAATTTTTTTCCAAC | 4331 |
rs75156911 | snp | G/T | 0.5 | 0 | intron-variant | MNAT1 | GRCh38.p7 | 14:60737866 | CTTTTTTTTTTTTTT[G/T]GAGAAGGAGTCTCGC | 4331 |
rs75188240 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | MNAT1 | GRCh38.p7 | 14:60758217 | GACTTTTTTTTTTTT[C/T]TCTTTTTGAGGTAGG | 4331 |
rs75189553 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | MNAT1 | GRCh38.p7 | 14:60735231 | ACTGTATTTCCAGGC[C/T]TTGTGTTGTTTACTG | 4331 |
rs75213664 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | MNAT1 | GRCh38.p7 | 14:60905218 | ATTCTCCTGTAATAA[A/G]ACCAACAATAACAGT | 4331 |
rs75278920 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | MNAT1 | GRCh38.p7 | 14:60753534 | TGTTCGCACAACATA[A/G]TAGCTTTCTTCTCCT | 4331 |
rs75323085 | snp | C/T | 0.199564 | 0.24486 | intron-variant | MNAT1 | GRCh38.p7 | 14:60888216 | aaaatattggcaaac[C/T]gaatccagcagcaca | 4331 |
rs75339885 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | MNAT1 | GRCh38.p7 | 14:60868218 | ACATCCATATACATA[C/T]GTACAAATAGACATA | 4331 |
rs75349496 | snp | A/G | 0.0486741 | 0.148216 | intron-variant | MNAT1 | GRCh38.p7 | 14:60792835 | AAAATATTTTTGGAA[A/G]TGGATAATGACTGAA | 4331 |
rs75373338 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | MNAT1 | GRCh38.p7 | 14:60785788 | AGCTTTGCATTTGAC[A/G]AGGCACCTGGCATAG | 4331 |
rs75386227 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | MNAT1 | GRCh38.p7 | 14:60960625 | CCCACCCTTAATTGC[C/T]TCTCCAGTTTTCTAT | 4331 |
rs75408119 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | MNAT1 | GRCh38.p7 | 14:60961918 | TAGACAAACCAGAAT[C/G]AGGCACTAGGTTTTT | 4331 |
rs75420326 | snp | G/T | 0.0170251 | 0.090679 | intron-variant | MNAT1 | GRCh38.p7 | 14:60908006 | TCCAGGTGACTATGA[G/T]CAGAGATAAATTGAT | 4331 |
rs75451329 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | MNAT1 | GRCh38.p7 | 14:60893900 | TTTCCAACGTTAGTC[A/G]TAGGAGGACCTGTGT | 4331 |
rs75452497 | in-del | -/CCT | | | intron-variant | MNAT1 | GRCh38.p7 | 14:60867727 | TCCTCACTTATACAC[-/CCT]TCCCCCCTTCCTCAT | 4331 |
rs75458762 | snp | A/T | | | intron-variant | MNAT1 | GRCh38.p7 | 14:60943627 | TTCTCTTTTTTTTTT[A/T]AATTCCTAAACATTT | 4331 |
rs75463513 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | MNAT1 | GRCh38.p7 | 14:60927096 | GTATGGTTCTTATTA[C/T]TTCAAAGTTAATTTA | 4331 |
rs75524995 | snp | A/T | 0.5 | 0 | intron-variant | MNAT1 | GRCh38.p7 | 14:60902948 | GGAGTCAGTCAGCTG[A/T]AAAAAAATTTTTTTT | 4331 |
rs75535113 | snp | A/T | 0.11228 | 0.208646 | intron-variant | MNAT1 | GRCh38.p7 | 14:60782901 | CACTTAGCAGACATA[A/T]CTTTGTTCTGTTGTT | 4331 |
rs75570952 | snp | G/T | 0.0123036 | 0.0774623 | intron-variant | MNAT1 | GRCh38.p7 | 14:60959361 | AATAATGATTTCTGC[G/T]TATATGGCTGATACT | 4331 |
rs75571112 | snp | A/G | 0.0471551 | 0.14613 | intron-variant | MNAT1 | GRCh38.p7 | 14:60826970 | AACAAGCGAAGGCAC[A/G]TTGGTCATCTCATAA | 4331 |
rs75572539 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | MNAT1 | GRCh38.p7 | 14:60842137 | TTTTATTGTAACATA[A/G]CCATTCTCATTCATT | 4331 |
rs75575169 | snp | G/T | 0.0232847 | 0.105357 | intron-variant | MNAT1 | GRCh38.p7 | 14:60789398 | GAGAATTACCAAAAT[G/T]TGAAACAGAGACGTG | 4331 |
rs75657701 | snp | A/G | 0.212122 | 0.247114 | intron-variant | MNAT1 | GRCh38.p7 | 14:60956125 | TTCTTTTTAAGTATT[A/G]TCTTTTATTAGTATA | 4331 |
rs75767379 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | MNAT1 | GRCh38.p7 | 14:60794896 | CCTTTGTCTTGTATT[C/T]ATTTTTTTGTTTTGT | 4331 |
rs75790936 | snp | C/G | | | intron-variant | MNAT1 | GRCh38.p7 | 14:60915041 | ATTCTATGTAGGTTT[C/G]TTTTTTATTTGACCG | 4331 |
rs75845874 | snp | C/T | 0.0452528 | 0.143452 | intron-variant | MNAT1 | GRCh38.p7 | 14:60859512 | TGGGAAATATGAAGA[C/T]GAAAAAAATTGGCCC | 4331 |
rs75852033 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | MNAT1 | GRCh38.p7 | 14:60737393 | CATAAACATATATAT[A/G]TGTGTGTATATATAT | 4331 |
rs75854338 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | MNAT1 | GRCh38.p7 | 14:60870602 | CCTGTCATTTTGATG[C/G]TGATAGCAAAATTTC | 4331 |
rs75890275 | snp | C/T | 0 | 0 | intron-variant | MNAT1 | GRCh38.p7 | 14:60820551 | CTTTTTTTTTTTTTT[C/T]CAGTTGCTGACTATA | 4331 |
rs75917195 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | MNAT1 | GRCh38.p7 | 14:60789445 | TTGGAAAAATGGTGC[A/C/T]GATAGACTCATTCCA | 4331 |
rs75965600 | snp | G/T | 0.5 | 0 | intron-variant | MNAT1 | GRCh38.p7 | 14:60766495 | AAGGCCGGTGGATCA[G/T]GACGTCAGGAGATCG | 4331 |
rs75970555 | snp | A/G | 0.0410537 | 0.137264 | upstream-variant-2KB | MNAT1 | GRCh38.p7 | 14:60732903 | AAAGCAATTCACTTC[A/G]CAACGTGGTTGGGGT | 4331 |
rs76019404 | snp | C/T | 0.219648 | 0.248151 | intron-variant | MNAT1 | GRCh38.p7 | 14:60900909 | GGAGAATCACCTGAG[C/T]CTGGGGAGGTTGAGG | 4331 |
rs76033478 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | MNAT1 | GRCh38.p7 | 14:60957521 | GAGGTAAATGAATCA[C/G/T]GGGAGCAGATCTTTC | 4331 |
rs76034891 | snp | G/T | 0.5 | 0 | intron-variant | MNAT1 | GRCh38.p7 | 14:60954470 | TTTTAAATTGTTGGG[G/T]TTTTTTGTTTTGTTT | 4331 |
rs76052348 | snp | C/T | 0.0633504 | 0.166319 | intron-variant | MNAT1 | GRCh38.p7 | 14:60791894 | AATTCCAGTTTAATT[C/T]CCACTTGAAAGCTGA | 4331 |
rs76064540 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | MNAT1 | GRCh38.p7 | 14:60865192 | ATCTTTTCACGGAAA[A/G]ATATTTCTGCTTTAG | 4331 |
rs76188850 | snp | A/T | 0.5 | 0 | intron-variant | MNAT1 | GRCh38.p7 | 14:60936233 | TTTTTGTGTGTGTGC[A/T]TTTTTTTTATTATAC | 4331 |
rs76206529 | snp | G/T | 0.0260105 | 0.111035 | intron-variant | MNAT1 | GRCh38.p7 | 14:60813907 | TGTAACTCTAAGAAC[G/T]ATGTTAAAATGAGGT | 4331 |
rs76225166 | snp | A/T | 0.5 | 0 | intron-variant | MNAT1 | GRCh38.p7 | 14:60740163 | CCATCTTAAAAAAAA[A/T]TTAATTTCTATCCCA | 4331 |
rs76254264 | snp | C/G | 0 | 0 | intron-variant | MNAT1 | GRCh38.p7 | 14:60854782 | AGGCACAGGGGTCAG[C/G]GAACCATTTGAGGAG | 4331 |
rs76269033 | snp | G/T | 0 | 0 | intron-variant | MNAT1 | GRCh38.p7 | 14:60802948 | TTTTTTTTTTTTTTT[G/T]TTGAGACGGAGTTTC | 4331 |
rs76339526 | snp | C/T | 0.0260105 | 0.111035 | upstream-variant-2KB | MNAT1 | GRCh38.p7 | 14:60734355 | TGATGGAGTAGATAG[C/T]TTTTTCATATTTTGT | 4331 |
rs76354146 | snp | A/G/T | 0.00636936 | 0.0560724 | intron-variant | MNAT1 | GRCh38.p7 | 14:60910598 | TCATGTTTTTTTGTC[A/G/T]TTGGTTCTGTTAATA | 4331 |
rs76362411 | snp | C/T | 0 | 0 | intron-variant | MNAT1 | GRCh38.p7 | 14:60826313 | ATAGGAGAAATTTTT[C/T]TTTTTTTTTTTTTTT | 4331 |
rs76385159 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | MNAT1 | GRCh38.p7 | 14:60872978 | CACTGACCTTTTCCT[C/G]CATAGGACATTCTCA | 4331 |
rs76402889 | snp | C/G | 0 | 0 | intron-variant | MNAT1 | GRCh38.p7 | 14:60854613 | AGACCCTGTTTGCCT[C/G]GGTATCACCAGTGGA | 4331 |
rs76444214 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | MNAT1 | GRCh38.p7 | 14:60820767 | AGCCTTTGGGTGGTT[C/T]CCTAAATAAATGAAT | 4331 |
rs76446113 | snp | A/G/T | 0.0115206 | 0.075079 | intron-variant | MNAT1 | GRCh38.p7 | 14:60957220 | ACATCTTATAGTTAC[A/G/T]CTAGTCATACAAAAA | 4331 |
rs76459444 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | MNAT1 | GRCh38.p7 | 14:60743820 | TTCTTTAGATTATAT[A/G]TTTTCTATTGATCTA | 4331 |
rs76469771 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | MNAT1 | GRCh38.p7 | 14:60792238 | TTAGGTCATTTCTAC[C/T]TCTAAAATTTCTATG | 4331 |
rs76480820 | snp | G/T | 0.5 | 0 | intron-variant | MNAT1 | GRCh38.p7 | 14:60917662 | GAGTCTCACTTTTTT[G/T]CCCAGGCTGGAGTGG | 4331 |
rs76523491 | snp | A/C | 0.0252325 | 0.109451 | intron-variant | MNAT1 | GRCh38.p7 | 14:60943234 | TCAGATTTAACTTCT[A/C]TAGATCTGAGTCACT | 4331 |
rs76548974 | snp | A/T | 0.0103295 | 0.0711199 | intron-variant | MNAT1 | GRCh38.p7 | 14:60934889 | ATGCCTCACTTTCCC[A/T]AGTTTATCAAGGGTT | 4331 |
rs76564589 | snp | A/T | 0.121369 | 0.214369 | intron-variant | MNAT1 | GRCh38.p7 | 14:60897633 | TACATAATATTTTAC[A/T]TATTTATGGGGTACA | 4331 |
rs76568192 | snp | A/G | 4.96685e-05 | 0.00498315 | missense | MNAT1 | GRCh38.p7 | 14:60879765 | GAAGAAGCTCTGTAT[A/G]AATACCAGCCACTGC | 4331 |
rs76591393 | snp | A/C/T | 0.0150606 | 0.0854603 | intron-variant | MNAT1 | GRCh38.p7 | 14:60839982 | GTGGAATGAGCCCAG[A/C/T]GGGCCCAAGAAAACT | 4331 |
rs76614015 | in-del | -/A | 0.40853 | 0.193309 | intron-variant | MNAT1 | GRCh38.p7 | 14:60918757 | TATATATATATATAT[-/A]TTTTGTCCTTAAAAA | 4331 |
rs76617909 | snp | A/G/T | 0.0146672 | 0.084371 | intron-variant, upstream-variant-2KB | MNAT1 | GRCh38.p7 | 14:60790509 | GGAAGCCCCCACTTC[A/G/T]ACTTGTCCCACCTTA | 4331 |
rs76620788 | snp | A/G | 0.5 | 0 | intron-variant | MNAT1 | GRCh38.p7 | 14:60748198 | CGAGACTCTGTCTCA[A/G]AAAAAAAAAAAAAGA | 4331 |
rs76646209 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | MNAT1 | GRCh38.p7 | 14:60919967 | ATGATGCCATCCAAC[A/G]CCATCATGTTGCCAT | 4331 |
rs76646997 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | MNAT1 | GRCh38.p7 | 14:60818499 | AGGAACTTTTAATGT[A/G]GATTTTATAAAAATA | 4331 |
rs76649316 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | MNAT1 | GRCh38.p7 | 14:60867112 | TGGCTTGCCAAGTGA[A/G]GATGTATTTAGAGCC | 4331 |
rs76665882 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | MNAT1 | GRCh38.p7 | 14:60749561 | TTTCTCATCTGTACA[A/G]TGGGTTCACTAGTAG | 4331 |
rs76803864 | snp | G/T | 0.5 | 0 | intron-variant | MNAT1 | GRCh38.p7 | 14:60784869 | ACACTTTTTTTTTTT[G/T]GAGAACGAGTCTCAA | 4331 |
rs76813810 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | MNAT1 | GRCh38.p7 | 14:60959220 | GCAGAGCAAGCTGCC[A/G]TGGTCCACCTCAGTG | 4331 |
rs76831779 | snp | A/T | | | intron-variant | MNAT1 | GRCh38.p7 | 14:60740354 | TTTTTTTCCCTTTTT[A/T]TTCTGTTCTCCTATT | 4331 |
rs76846583 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | MNAT1 | GRCh38.p7 | 14:60845445 | TGCTAATTTTTAGCA[A/G]ATTCCCAGCACTCTG | 4331 |
rs76859743 | snp | A/C/T | 0.0599851 | 0.162463 | intron-variant | MNAT1 | GRCh38.p7 | 14:60742059 | TATTGGCCTATTAGC[A/C/T]GGTAGCTTTTTATTT | 4331 |
rs76862540 | snp | A/G | 0.0279526 | 0.114869 | intron-variant | MNAT1 | GRCh38.p7 | 14:60782734 | TTTATTTCTCACAAG[A/G]AAGGAAACAGAGGCA | 4331 |
rs76874519 | snp | A/G | 0.5 | 0 | intron-variant | MNAT1 | GRCh38.p7 | 14:60766452 | GGCGTGGTGGCTCAG[A/G]CCTGTAATCCCAGCA | 4331 |
rs76879799 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | MNAT1 | GRCh38.p7 | 14:60884753 | TTACAGTGTGGGAAT[A/G]TTCTGTGTTTTTCTG | 4331 |
rs76902117 | snp | C/T | 0.5 | 0 | intron-variant | MNAT1 | GRCh38.p7 | 14:60958599 | TATTTCTTTCTCTTT[C/T]TCTTTCTTTCTTTTT | 4331 |
rs76936392 | snp | C/T | 0.0901694 | 0.192235 | intron-variant | MNAT1 | GRCh38.p7 | 14:60859215 | GACCCAGGCATATCT[C/T]TTGCCTATTTTGGTG | 4331 |
rs76954877 | snp | A/T | 0.5 | 0 | intron-variant | MNAT1 | GRCh38.p7 | 14:60769672 | AAAATTTGTTTTTTT[A/T]AGAGACAGGGCCTTA | 4331 |
rs76977763 | snp | A/C | | | intron-variant | MNAT1 | GRCh38.p7 | 14:60744612 | TAGTTCAGTTACTGG[A/C]AGATAACTTTGAACT | 4331 |
rs77016784 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | MNAT1 | GRCh38.p7 | 14:60935325 | GCCCCCATCCCTCCC[C/T]CCCTCCCTCCTTCCT | 4331 |
rs77026055 | snp | C/T | 0.5 | 0 | intron-variant | MNAT1 | GRCh38.p7 | 14:60781310 | GGTGTAATTTGCCTG[C/T]TCATATAATCCACTC | 4331 |
rs77040636 | snp | G/T | 0.5 | 0 | intron-variant | MNAT1 | GRCh38.p7 | 14:60917661 | GGAGTCTCACTTTTT[G/T]GCCCAGGCTGGAGTG | 4331 |
rs77043444 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | MNAT1 | GRCh38.p7 | 14:60809124 | TTGTCTAATTTATAC[A/C]CTTTAGCTATCATTT | 4331 |
rs77116300 | snp | C/T | 0.127944 | 0.218179 | intron-variant | MNAT1 | GRCh38.p7 | 14:60849845 | TAGTTTCTTTCTTTC[C/T]TTTTTTTTTTAAATG | 4331 |
rs77176194 | snp | A/C | 0.5 | 0 | intron-variant | MNAT1 | GRCh38.p7 | 14:60824156 | AGTGAGACTCCATCT[A/C]AAAAAAAAAATAATA | 4331 |
rs77190764 | snp | A/C | 0.5 | 0 | intron-variant | MNAT1 | GRCh38.p7 | 14:60769484 | AGATGGGGTCTTGCT[A/C]TGTTGTCCAGGCTAG | 4331 |
rs77192990 | snp | A/G | 0.0279526 | 0.114869 | intron-variant | MNAT1 | GRCh38.p7 | 14:60776069 | GATGGCTTCAACCAT[A/G]GATGGATCAGGTGGA | 4331 |
rs77235525 | snp | A/T | 0.5 | 0 | intron-variant | MNAT1 | GRCh38.p7 | 14:60784359 | TTTTTTTTTTTTTAA[A/T]TAGAGATGAGGGTCT | 4331 |
rs77285512 | snp | G/T | 0.084728 | 0.187577 | intron-variant | MNAT1 | GRCh38.p7 | 14:60830590 | GCGATGATTTTTAAT[G/T]TAATATTTTAATTTT | 4331 |
rs77301652 | in-del | -/T | 0.274106 | 0.254834 | intron-variant | MNAT1 | GRCh38.p7 | 14:60903135 | TTCGCTGTTTAAGTG[-/T]TTTTTTTGTATCACA | 4331 |
rs77304340 | snp | C/T | | | intron-variant | MNAT1 | GRCh38.p7 | 14:60915039 | TGATTCTATGTAGGT[C/T]TGTTTTTTATTTGAC | 4331 |
rs77310234 | snp | A/C/T | 0.0023933 | 0.0345097 | intron-variant | MNAT1 | GRCh38.p7 | 14:60867283 | GTCTGCAGGATGAAA[A/C/T]CTCTTTTTTTATTTT | 4331 |
rs77360751 | snp | C/G | 0.0260105 | 0.111035 | intron-variant, utr-variant-5-prime | MNAT1 | GRCh38.p7 | 14:60799545 | AAATTATAGGTGTTG[C/G]AGTACAAGTTGAATA | 4331 |
rs77366607 | snp | A/G | 0.5 | 0 | intron-variant | MNAT1 | GRCh38.p7 | 14:60945355 | AGAGCCCTTTGCCAG[A/G]AAAAAAAAATAGAGC | 4331 |
rs77395121 | snp | A/C | 0.030665 | 0.119967 | intron-variant | MNAT1 | GRCh38.p7 | 14:60956804 | TGTTTTGTCTGATGT[A/C]AGTTTACCTGTCCCT | 4331 |
rs77422490 | snp | G/T | 0.5 | 0 | intron-variant | MNAT1 | GRCh38.p7 | 14:60784870 | CACTTTTTTTTTTTT[G/T]AGAACGAGTCTCAAC | 4331 |
rs77575348 | snp | G/T | 0 | 0 | intron-variant | MNAT1 | GRCh38.p7 | 14:60959935 | GTTTTTTTTTTTTTT[G/T]TTGCTAAGCATTGTT | 4331 |
rs77587008 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | MNAT1 | GRCh38.p7 | 14:60880942 | CAATATTGCGTTTTA[C/T]AATGTAAAAAGTTAT | 4331 |
rs77592594 | in-del | -/TTTTT | | | intron-variant | MNAT1 | GRCh38.p7 | 14:60741654 | TGAGCCACTGCGCCT[-/TTTTT]GGGGTTTTTTTTTTT | 4331 |
rs77599113 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | MNAT1 | GRCh38.p7 | 14:60801271 | AAAACATGAGGGATG[A/C]CTAAAAATGGGGCCT | 4331 |
rs77622926 | snp | A/G | | | intron-variant | MNAT1 | GRCh38.p7 | 14:60917305 | CCTCATTTTACCAGG[A/G]AAAAATAGTCATTCC | 4331 |
rs77634395 | snp | A/G | 0.5 | 0 | intron-variant | MNAT1 | GRCh38.p7 | 14:60945354 | CAGAGCCCTTTGCCA[A/G]AAAAAAAAAATAGAG | 4331 |
rs77637309 | snp | G/T | 0.0391387 | 0.134304 | intron-variant | MNAT1 | GRCh38.p7 | 14:60788056 | TGCCCAGATCTATCA[G/T]AGGAATCATTGTCTG | 4331 |
rs77642333 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | MNAT1 | GRCh38.p7 | 14:60742432 | GGTTTCTTTCAGCAT[A/G]TCTTTTATTTGTATT | 4331 |
rs77709238 | snp | G/T | | | intron-variant | MNAT1 | GRCh38.p7 | 14:60834998 | TGCTCCCGCCCTCCC[G/T]CCCTCCCTCCCTCTC | 4331 |
rs77749018 | snp | A/C | 0.0193772 | 0.0965046 | intron-variant | MNAT1 | GRCh38.p7 | 14:60777444 | CCACCTCTCCCCCCC[A/C]AAAATTTTTGTTTTT | 4331 |
rs77780261 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | MNAT1 | GRCh38.p7 | 14:60864778 | TATGAGTGTGATAGC[A/G]GTGGTGGTGGTGTTT | 4331 |
rs77882001 | in-del | -/AAA | | | intron-variant | MNAT1 | GRCh38.p7 | 14:60847418 | CAAAAAAAAAAAAAA[-/AAA]GACTTGTTTTATTTT | 4331 |
rs77887665 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | MNAT1 | GRCh38.p7 | 14:60756978 | CATTAGTGTATTTGA[C/T]CTGGACTAGAACTTG | 4331 |
rs77909942 | snp | A/C | 0.5 | 0 | intron-variant | MNAT1 | GRCh38.p7 | 14:60856545 | TCCTTCTACTGAAAG[A/C]TGATGCCATCTAGGA | 4331 |
rs77975020 | snp | A/T | 0.112983 | 0.209108 | intron-variant | MNAT1 | GRCh38.p7 | 14:60820949 | AAAATGGAGTTAGCC[A/T]TGCAAAAATACAGGC | 4331 |
rs77994811 | snp | G/T | 0.5 | 0 | intron-variant | MNAT1 | GRCh38.p7 | 14:60887204 | TACATATCAGAGCTG[G/T]TTTTTTTTCTTGTTT | 4331 |
rs78004690 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | MNAT1 | GRCh38.p7 | 14:60841874 | CTATCTGATGCCATA[C/T]GTATTTATTGAGAGG | 4331 |
rs78052829 | snp | A/G | | | intron-variant | MNAT1 | GRCh38.p7 | 14:60877437 | CTCACTGCTACAATT[A/G]TATTTTATGACTTTT | 4331 |
rs78061943 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | MNAT1 | GRCh38.p7 | 14:60740524 | ATCAGATTAAGTTTG[A/C]ATTTATTTGTTGATA | 4331 |
rs78066258 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | MNAT1 | GRCh38.p7 | 14:60882412 | TCAAATGACAGGATC[A/G]CATACCTTTTTTATG | 4331 |
rs78069923 | snp | G/T | 0.0142736 | 0.0832652 | intron-variant, utr-variant-5-prime | MNAT1 | GRCh38.p7 | 14:60799439 | AGTATAGGACAAGCT[G/T]TTGGATAGCAATTGG | 4331 |
rs78104565 | snp | C/G | 0.00597247 | 0.0543191 | utr-variant-3-prime, intron-variant | MNAT1 | GRCh38.p7 | 14:60968432 | TTATAGCTATGTGCA[C/G]CTGCACAACACAGTC | 4331 |
rs78157518 | snp | A/C | | | intron-variant | MNAT1 | GRCh38.p7 | 14:60834996 | CTTGCTCCCGCCCTC[A/C]CTCCCTCCCTCCCTC | 4331 |
rs78190937 | snp | C/T | 0.5 | 0 | intron-variant | MNAT1 | GRCh38.p7 | 14:60948523 | CATTGTAGAGTTTTT[C/T]CATTTCTAGAAAACC | 4331 |
rs78217912 | snp | G/T | 0.0123036 | 0.0774623 | intron-variant | MNAT1 | GRCh38.p7 | 14:60756108 | TTTCATTATGATGCT[G/T]AGATTATTTGATAGC | 4331 |
rs78236107 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | MNAT1 | GRCh38.p7 | 14:60788569 | TTCCAATAGAAGGAT[A/G]TTTCATCTGCATTGA | 4331 |
rs78241014 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | MNAT1 | GRCh38.p7 | 14:60743885 | AATCTCATCCAATAG[A/G]TTTTTCATTTCTTAT | 4331 |
rs78284006 | snp | A/T | 0.5 | 0 | intron-variant | MNAT1 | GRCh38.p7 | 14:60739388 | GGATTTTATTAACTT[A/T]TTTTTTTTTTTTTCA | 4331 |
rs78357761 | in-del | -/TT | | | intron-variant | MNAT1 | GRCh38.p7 | 14:60943626 | TTTCTCTTTTTTTTT[-/TT]AATTCCTAAACATTT | 4331 |
rs78400863 | snp | G/T | 0.5 | 0 | intron-variant | MNAT1 | GRCh38.p7 | 14:60826330 | TTTTTTTTTTTTTTT[G/T]TTTTGAGATGGAGTC | 4331 |
rs78402678 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MNAT1 | GRCh38.p7 | 14:60957641 | TCTTCTCTTATATTT[C/T]ATGTTTTCTGTGTCA | 4331 |
rs78447178 | snp | A/C | 0.211516 | 0.24702 | intron-variant | MNAT1 | GRCh38.p7 | 14:60943187 | CAACAATTGTGGTTC[A/C]TCTGATGCATACTGA | 4331 |
rs78456655 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | MNAT1 | GRCh38.p7 | 14:60867216 | TCAAGCATATCATGT[A/G]TATTTGAGTAGAACT | 4331 |
rs78484529 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MNAT1 | GRCh38.p7 | 14:60884330 | AAGTGATCATATGGT[G/T]TGGTCCTCACTCTGT | 4331 |
rs78503378 | snp | A/G | 0.0252325 | 0.109451 | intron-variant | MNAT1 | GRCh38.p7 | 14:60736619 | AAATGTGAACAAAAT[A/G]AGTGAAAAGCTGTAG | 4331 |
rs78551464 | snp | A/G | 0.0267878 | 0.112589 | intron-variant | MNAT1 | GRCh38.p7 | 14:60805135 | ATAAAAGTAATTATA[A/G]ATGTTGGGTATTAGT | 4331 |
rs78555167 | snp | A/G | 0.5 | 0 | intron-variant | MNAT1 | GRCh38.p7 | 14:60779816 | AAAAAGAAAAAAAAA[A/G]GAAGCTGTTTCCTGC | 4331 |
rs78586015 | snp | A/T | 0.0240643 | 0.107019 | intron-variant | MNAT1 | GRCh38.p7 | 14:60897660 | TACATGTGAATATTT[A/T]TACATGCATAGAATG | 4331 |
rs78591291 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | MNAT1 | GRCh38.p7 | 14:60833961 | TTCTAGTTTATCTTC[A/G]TAGAGGTGTTAATAG | 4331 |
rs78684486 | snp | C/G | 0.00953873 | 0.0683987 | intron-variant | MNAT1 | GRCh38.p7 | 14:60782567 | TCTGGTCCTTACTGG[C/G]TATTCCTTGTATTAA | 4331 |
rs78772182 | snp | C/G | 0.5 | 0 | intron-variant | MNAT1 | GRCh38.p7 | 14:60866367 | TCCTTGTGCATGTCA[C/G]AGTATAGCTGTGTTG | 4331 |
rs78886228 | snp | A/G | 0.5 | 0 | intron-variant | MNAT1 | GRCh38.p7 | 14:60748211 | CAGAAAAAAAAAAAA[A/G]GAAGAAAATATTTTA | 4331 |
rs78955844 | snp | G/T | 0.00953873 | 0.0683987 | intron-variant | MNAT1 | GRCh38.p7 | 14:60794071 | CCTTGCTGACTAAAC[G/T]ATTGATTGAGTCTAA | 4331 |
rs78963660 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | MNAT1 | GRCh38.p7 | 14:60921473 | AGTGGTCTCTGTTCT[C/T]AGGAAATATAAACCC | 4331 |
rs78978299 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MNAT1 | GRCh38.p7 | 14:60925565 | TTCCCAAGTTTTGCT[A/C]ATTTTGCTTGTTTTT | 4331 |
rs79006981 | snp | G/T | 0.5 | 0 | intron-variant | MNAT1 | GRCh38.p7 | 14:60847936 | TTACAGGTTTTTTTT[G/T]GTAGCTGTTTTGTAA | 4331 |
rs79011394 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | MNAT1 | GRCh38.p7 | 14:60953334 | AAAGATTAGCAAGCA[A/G]GATTCTTCTTATCCT | 4331 |
rs79036830 | snp | G/T | 0.0142736 | 0.0832652 | intron-variant | MNAT1 | GRCh38.p7 | 14:60895265 | GTTTTTCTTATTACT[G/T]TAGACCTAAAAATAT | 4331 |
rs79058636 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | MNAT1 | GRCh38.p7 | 14:60829493 | ATATTCTTTCCTTTA[A/C]CACGGTAAAGGAAAA | 4331 |
rs79069540 | snp | A/G | 0.0490535 | 0.14873 | intron-variant | MNAT1 | GRCh38.p7 | 14:60747254 | CTCCCAAAGTGCTAG[A/G]ATTACAGGCGTGAGC | 4331 |
rs79076384 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | MNAT1 | GRCh38.p7 | 14:60953862 | GTGATTTTAATTTGT[C/T]TTGCCTGGTGATTAG | 4331 |
rs79108430 | snp | A/G | 0.0256215 | 0.110247 | intron-variant | MNAT1 | GRCh38.p7 | 14:60759969 | ATAATATGGAAGTAG[A/G]TCTTCTGATTAGAAT | 4331 |
rs79108991 | snp | G/T | 0.213635 | 0.247341 | intron-variant | MNAT1 | GRCh38.p7 | 14:60848756 | AAGGCTTATAATAAT[G/T]AAAGTATTGACTTTT | 4331 |
rs79115489 | snp | A/G | 0 | 0 | intron-variant | MNAT1 | GRCh38.p7 | 14:60911079 | AATCTAGAAGAAATG[A/G]ATAAATTCCTGGACA | 4331 |
rs79145041 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | MNAT1 | GRCh38.p7 | 14:60899659 | CTTGCTGAGCAAAAG[C/T]AATTGATTATCACAA | 4331 |
rs79146460 | snp | A/G | | | intron-variant | MNAT1 | GRCh38.p7 | 14:60924454 | ATAGATTAAGGTGGG[A/G]AAGCATTTTTTTTTC | 4331 |
rs79151684 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | MNAT1 | GRCh38.p7 | 14:60808966 | TACCGAAAGAGTAAC[A/G]TTGCTAGATATAAAT | 4331 |
rs79152037 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | MNAT1 | GRCh38.p7 | 14:60838582 | GTCACTGCAAAGACA[C/T]CAGCTGCAGTGGGGA | 4331 |
rs79165762 | snp | A/C | | | intron-variant | MNAT1 | GRCh38.p7 | 14:60867852 | CTCAGCCTGTAGGCC[A/C]TGTCCCTCATTTGTC | 4331 |
rs79189444 | snp | G/T | 0.5 | 0 | intron-variant | MNAT1 | GRCh38.p7 | 14:60838311 | TGGCGAATTTTTTTT[G/T]GTTTTTAGGAGAGAC | 4331 |
rs79190641 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | MNAT1 | GRCh38.p7 | 14:60755919 | GTATAGAGATAGTCA[C/T]TGAGAGGAGAGGCTG | 4331 |
rs79234055 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | MNAT1 | GRCh38.p7 | 14:60935450 | GCATTTTGATTCTTA[C/T]TGTTGCTTATTCATT | 4331 |
rs79251141 | snp | C/T | 0.5 | 0 | intron-variant | MNAT1 | GRCh38.p7 | 14:60766604 | GTAATCCCAGCTACT[C/T]GGGAGGCTGAGGCAC | 4331 |
rs79251581 | snp | A/T | 0 | 0 | intron-variant | MNAT1 | GRCh38.p7 | 14:60784178 | CCACCATGCCTGGCT[A/T]ATTTTTTTTTTTTTT | 4331 |
rs79272751 | snp | A/T | 0.5 | 0 | intron-variant | MNAT1 | GRCh38.p7 | 14:60769660 | AAAATTAAAAAAAAA[A/T]TTTGTTTTTTTTAGA | 4331 |
rs79336751 | snp | G/T | 0.00914312 | 0.0669923 | intron-variant | MNAT1 | GRCh38.p7 | 14:60841382 | TTTTTCATTTTAAAA[G/T]TGTGTGTGTTTTTAA | 4331 |
rs79340845 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | MNAT1 | GRCh38.p7 | 14:60822568 | GTAACTGGGTTTACA[A/G]GCTCACACCACCACT | 4331 |
rs79350932 | snp | A/G | 0.0444908 | 0.142359 | intron-variant | MNAT1 | GRCh38.p7 | 14:60918605 | TGTATCAACTAAATT[A/G]TGGTGCACAAACATC | 4331 |
rs79351583 | snp | A/G | 0.0693013 | 0.172766 | intron-variant | MNAT1 | GRCh38.p7 | 14:60747252 | GCCTCCCAAAGTGCT[A/G]GGATTACAGGCGTGA | 4331 |
rs79358926 | snp | C/G | 0.5 | 0 | intron-variant | MNAT1 | GRCh38.p7 | 14:60835912 | GAACAAAGCCTCCAA[C/G]AAATATGGGACTATG | 4331 |
rs79369199 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | MNAT1 | GRCh38.p7 | 14:60810810 | TGTGCTTGGGAAGAT[C/T]GTGTATTCCGCTGCT | 4331 |
rs79388534 | snp | A/T | 0.5 | 0 | intron-variant | MNAT1 | GRCh38.p7 | 14:60771240 | TCAGACTTTAAAATT[A/T]AAAAAAAAATTCAGA | 4331 |
rs79400184 | snp | A/G | 0.0562307 | 0.157967 | intron-variant | MNAT1 | GRCh38.p7 | 14:60956496 | TGGCTGGAATTTTCT[A/G]TATACGTCTGTTAGG | 4331 |
rs79444114 | snp | C/G/T | 0.0341544 | 0.126217 | intron-variant | MNAT1 | GRCh38.p7 | 14:60876814 | ATACACACCACATAT[C/G/T]GTTTATTCATTTATT | 4331 |
rs79448735 | snp | A/T | 0.5 | 0 | intron-variant | MNAT1 | GRCh38.p7 | 14:60739390 | ATTTTATTAACTTAT[A/T]TTTTTTTTTTTCATG | 4331 |
rs79456231 | snp | A/T | 0 | 0 | intron-variant | MNAT1 | GRCh38.p7 | 14:60754524 | GGTTGATTTTTTTTT[A/T]ATTTTTAGTAGAGAC | 4331 |
rs79461168 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | MNAT1 | GRCh38.p7 | 14:60781211 | CAGAACTCTTAAAAA[C/T]TTTTTTTTGTGTTTT | 4331 |
rs79462729 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | MNAT1 | GRCh38.p7 | 14:60753551 | AGCTTTCTTCTCCTC[A/G]GGTGGATGATTCAAG | 4331 |