SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs13264 | snp | C/T | 0 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46428743 | TGTGCCACCTGGTGC[C/T]GACAAGAAAGCCGAG | 55626 |
rs14196 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46428777 | GGGAAGCTGACAGAG[A/G]TACCTACAGACGGAG | 55626 |
rs713120 | snp | A/G | 0 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46529050 | GGAGTAGAAAATTGT[A/G]ATAATAAAGGAATCA | 55626 |
rs756343 | snp | G/T | 0.101301 | 0.200969 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46528726 | TTAATAATTTTAAAA[G/T]TGTACAGTACACATT | 55626 |
rs870242 | snp | C/T | 0 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46496432 | AGAAAAGAAGCATCA[C/T]GGGTCAAATCTAATT | 55626 |
rs901997 | snp | G/T | 0.014507 | 0.0839229 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46505354 | ATTCAGTTTACTGTA[G/T]AGGGAGGTGGGCAGG | 55626 |
rs901999 | snp | A/C | 0.0418186 | 0.138422 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46404874 | GGGCTGCATGCTAAC[A/C]AAGAAAACAGCAGAG | 55626 |
rs931402 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46432043 | tatttttatttattt[A/G/T]tttttttttGAGATT | 55626 |
rs967754 | snp | C/T | 0.0298908 | 0.118541 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46415239 | TTCATGTCTTTTGAG[C/T]GGTCTACAGATGAGT | 55626 |
rs1052395 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46428752 | ACGGAGTGCTGTGCC[A/C]CCTGGTGCCGACAAG | 55626 |
rs1140566 | snp | C/T | 0 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46428769 | GCACAGCACTCCGTC[C/T]GTAGGTATCTCTGTC | 55626 |
rs1140567 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46428771 | ACAGCACTCCGTCTG[C/T]AGGTATCTCTGTCAG | 55626 |
rs1466634 | snp | A/C | 0.0170251 | 0.090679 | utr-variant-3-prime, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46396508 | TTCTGTTTGTAACTC[A/C]TCATAGAAACATTGT | 55626 |
rs1466635 | snp | C/T | 0.110872 | 0.20771 | downstream-variant-500B | AMBRA1 | GRCh38.p7 | 11:46396265 | CCCCTCTGACCCCTT[C/T]GCCAGAGCTGGTCAG | 55626 |
rs1472000 | snp | G/T | 0.0109286 | 0.0731087 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46444276 | TCAAGGAGGTTCTTA[G/T]GGGGTAGGTATTATA | 55626 |
rs1472001 | snp | A/G | 0.289165 | 0.246913 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46463135 | GCCCCATGGCACTTT[A/G]TTTCTCTCTTATTCT | 55626 |
rs1489189 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46509714 | TGTATACACTAATAC[A/G]TATACTAAAATATGT | 55626 |
rs1489190 | snp | C/T | 0.0314385 | 0.121371 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46509900 | GATTAAGAACAGAAA[C/T]AGGAATAGTTATATC | 55626 |
rs1489191 | snp | A/G | 0 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46509933 | AATGGTACAAAAAGT[A/G]TTGGCAACTATCTTG | 55626 |
rs1489192 | snp | A/G | 0.312348 | 0.242101 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46487794 | GGGTTTTTGTCTGCC[A/G]TTTTACTGTTTGTTT | 55626 |
rs1489193 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46463649 | AAGATACCCACTCAA[C/T]CGTCAGAATGGCACT | 55626 |
rs1812657 | snp | C/G | 0.0298908 | 0.118541 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46427738 | AACAGGCCGGGAGCG[C/G]TGGCTCATGCCTGTA | 55626 |
rs1873129 | snp | A/G | 0.0298908 | 0.118541 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46479865 | cttgtttaagccact[A/G]agtttctgcttgttg | 55626 |
rs1873130 | snp | A/G | 0.138886 | 0.22395 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46535971 | ACATCAGAGGTCACC[A/G]GAGCTCAAGTTTTGG | 55626 |
rs2014722 | snp | C/G | 0.0107246 | 0.0724382 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46496896 | tcgaacttctaactt[C/G]aagtgatctgcccgc | 55626 |
rs2029378 | snp | A/G | 0.0298908 | 0.118541 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46433248 | CTTGCAGGCCTCTGG[A/G]GAATGCAGCACATAT | 55626 |
rs2046766 | snp | A/C | 0.0298908 | 0.118541 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46425914 | CACTTTGGGAGGCTG[A/C]GGTGGGCAGATCACA | 55626 |
rs2046767 | snp | A/G | 0.0298908 | 0.118541 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46429962 | AGAGTAGCATATCCA[A/G]TCTGGAGGAATCGCA | 55626 |
rs2171667 | snp | C/G | 0.329691 | 0.24138 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46445542 | CCTTTTAATAAAGTC[C/G]TTCAGGTATCTTACC | 55626 |
rs2171668 | snp | G/T | 0.322483 | 0.239262 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46445278 | GGATGTCTTGTTTTG[G/T]GGGTATTCATTTATC | 55626 |
rs2291487 | snp | C/T | 0.201727 | 0.245295 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46434794 | CTCACCTAGCAATGA[C/T]CATGCCAAGGCACCA | 55626 |
rs2864071 | snp | A/G | 0.030278 | 0.119257 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46405230 | aggagtctcccctaa[A/G]ccccacaggctgggc | 55626 |
rs2864072 | snp | G/T | 0.312593 | 0.242037 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46447309 | GACCTCAAGTGATCC[G/T]CCTGCCTTGGCCTCA | 55626 |
rs2864076 | snp | A/G | 0.319136 | 0.24025 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46438488 | CTGCTAATTGCTCCC[A/G]TGGCCTCATCTGGCC | 55626 |
rs2864834 | snp | C/T | 0.030278 | 0.119257 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46428592 | CTTCTTCTTCTTCTT[C/T]TTTTTTTTTTAAGGT | 55626 |
rs2864835 | snp | C/T | 0 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46429099 | CCACCATGACTCCCT[C/T]CTTAAAAAGGAGTTC | 55626 |
rs2864836 | snp | C/T | 0.00757384 | 0.0610701 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542541 | ATGGCGAATGCTGCC[C/T]GAGTTGTTTTGGCTG | 55626 |
rs2902858 | snp | C/T | 0.322959 | 0.239117 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46502463 | GAAGTAGATAATACC[C/T]TATCCCTCTCTGACG | 55626 |
rs3071087 | in-del | -/AT | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46528754 | taagagggtaaatct[-/AT]gttatgttttctatc | 55626 |
rs3178098 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46428607 | ACTTATAGCCAAAAA[A/C]CCTTAAaaaaaaaag | 55626 |
rs3179874 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46428591 | CCTTAAaaaaaaaag[A/T]agaagaagaagaaga | 55626 |
rs3180415 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46428613 | GAATAAACTTATAGC[A/C]AAAAAACCTTAAaaa | 55626 |
rs3206777 | snp | C/T | 0 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46514038 | TCTCTGAGACCATTT[C/T]CTTTGAAACATGTTC | 55626 |
rs3210531 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46428800 | GCGACCTGCGAGACT[C/G]ACAAGAGGGGAAGCT | 55626 |
rs3740973 | snp | A/G | 0.48995 | 0.0701706 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46400687 | AGAGACGGTTTCGCC[A/G]TGTTGCCCAGGCTGG | 55626 |
rs3802887 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46429849 | TCAGCTCAGCAGTCT[C/G]TAAAAGCTTAACCTA | 55626 |
rs3802888 | snp | A/G | 0.375399 | 0.216275 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46494352 | GCTCACTAATTAGGC[A/G]GCACATTAATAAAAC | 55626 |
rs3802889 | snp | C/G/T | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46512964 | CTTCTACAAGCTAAG[C/G/T]AGGTAGAGACACAAA | 55626 |
rs3802890 | snp | A/G | 0.489837 | 0.0705577 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46512996 | AAATGAAGAGCTGCA[A/G]AACTCCCACACTGGA | 55626 |
rs3839953 | in-del | -/A | 0.0821764 | 0.185298 | intron-variant, frameshift-variant | AMBRA1 | GRCh38.p7 | 11:46431083 | ACGTAAGGGGCAACC[-/A]AGACCTGGAAAACCA | 55626 |
rs3897850 | snp | G/T | 0 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46492230 | CTCTGTCAGACACCA[G/T]GACTTCATAGGCTCT | 55626 |
rs3961051 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46428994 | CGTAGCCTCGGGACT[A/T]GAGAGACTGCATGGC | 55626 |
rs3975806 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46429010 | GAGAGACTGCATGGC[C/T]TTCATGACATGAAGG | 55626 |
rs3976777 | in-del | -/GTT | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46487341 | aacaagtaaattgtt[-/GTT]nnaaccaaaaataaa | 55626 |
rs4376875 | snp | C/T | 0.0298908 | 0.118541 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46429645 | TCTTTCTGGTTTCAT[C/T]AGTAATTTTGTATTT | 55626 |
rs4433539 | snp | C/T | 0.0298908 | 0.118541 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46420230 | TCCAAATGTAAGGAA[C/T]TCGTTAAGGCTCCTT | 55626 |
rs4508179 | snp | A/G | 0.0298908 | 0.118541 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46403924 | AATCTGTGTGGCTGC[A/G]TGTGGCGGCTCACGC | 55626 |
rs4550197 | snp | C/T | 0.0314385 | 0.121371 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46424454 | CTTTCCAAAGGCCAC[C/T]CCTGGCCATTAGGAT | 55626 |
rs4568980 | snp | G/T | 0.0926964 | 0.194308 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46517933 | ATTCGTATATATATA[G/T]AGAGAGAGAGAACAA | 55626 |
rs4752802 | snp | C/G | 0 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46577840 | ctataatcccagcta[C/G]tcaggaggctgaggc | 55626 |
rs4995987 | snp | A/G | | | intron-variant, upstream-variant-2KB, downstream-variant-500B | AMBRA1, MIR3160-1, MIR3160-2 | GRCh38.p7 | 11:46452262 | TTCATTTGTTTACCA[A/G]CTCACTGTGTATCTT | 55626 |
rs6485680 | snp | A/T | 0.138207 | 0.223612 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46421433 | CCTCCTGGATCCTGA[A/T]AAGCACTTGCTTGCT | 55626 |
rs6485681 | snp | C/T | 0.0298908 | 0.118541 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46421699 | CTCACTGAAGGGAAA[C/T]ACCTCTCACAATTAG | 55626 |
rs6485682 | snp | A/C | 0.3742 | 0.216966 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46424714 | gcatggtggcacata[A/C]ctctaatcctagcta | 55626 |
rs7101862 | snp | A/G | 0 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46466502 | AGCATGTGGAAAGGA[A/G]AATGGTTCAGGATAG | 55626 |
rs7104073 | snp | C/G | 0.375399 | 0.216275 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46574469 | taaatgtcttctttt[C/G]agaagtgtctgttca | 55626 |
rs7106740 | snp | A/T | 0.0174175 | 0.0916809 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46489947 | ccaggtcagcctctc[A/T]cagtgatattgggca | 55626 |
rs7109222 | snp | C/T | 0 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46529567 | GAGCTAATGCAATGG[C/T]CAAGTACACAAAATT | 55626 |
rs7110413 | snp | A/G | 0.0410537 | 0.137264 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46563516 | aggcatgagccacAC[A/G]GCACCCTGATGAGAA | 55626 |
rs7112229 | snp | C/T | 0.282895 | 0.247826 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46491699 | GGGAGTCTAGAGTTC[C/T]TTCTCCTAATGGCAT | 55626 |
rs7117179 | snp | A/G | 0 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46570347 | AGTCTCCTCCATGGA[A/G]CTATCCTGTGGGCCC | 55626 |
rs7117944 | snp | A/C | 0.0418186 | 0.138422 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46475878 | AGCAGGCAGCTTCAA[A/C]TAAAGGATATACTAA | 55626 |
rs7119921 | snp | A/T | 0.130694 | 0.219696 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46428133 | GGTATAAAGGGATAG[A/T]CCACTACTGACCAGC | 55626 |
rs7120080 | snp | C/G | 0 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46516003 | TACAATCCTAAAAGT[C/G]TATTTCCCACCTTAA | 55626 |
rs7121994 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46571555 | tggcacatacctgta[A/G]tcccagctactcagg | 55626 |
rs7123865 | snp | C/T | 0 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46432856 | TGAGCACCTATGGGA[C/T]GTGGGACGTTCACTC | 55626 |
rs7124013 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46524030 | tgcaccaccatgccc[A/G]gctaattttgtattt | 55626 |
rs7127529 | snp | A/C | 0.323908 | 0.238825 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46560522 | CCGGAAATAGAAAGC[A/C]ATAAGACCCAAATTT | 55626 |
rs7129348 | snp | A/T | 0.105214 | 0.203807 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46488500 | aagggaaaaatacac[A/T]attcaataataatag | 55626 |
rs7130028 | snp | C/T | 0.499897 | 0.00718776 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46556973 | gaaaccctgtctcta[C/T]taaaaatacaaaatt | 55626 |
rs7130141 | snp | C/T | 0.375598 | 0.21616 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46478324 | TTATAAATGATGCCA[C/T]GGGTACAGGTTCACT | 55626 |
rs7481312 | snp | C/T | 0.31357 | 0.241783 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46575124 | AAGTACCAGTGGTAT[C/T]AGTAACTCCCtctta | 55626 |
rs7482883 | snp | A/G | 0 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46577032 | ATCACATACTCTGGA[A/G]AAGCTGCAGATGTTG | 55626 |
rs7483199 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46484645 | ccaccacctatactt[C/G]tttggcttttttttt | 55626 |
rs7484125 | snp | C/T | 0.489376 | 0.0721049 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46566717 | taacagtaagaaaag[C/T]atgacagtgaaaaag | 55626 |
rs7924437 | snp | G/T | 0.0298908 | 0.118541 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46406058 | Ctttatttatttatt[G/T]tattattatttttga | 55626 |
rs7924695 | snp | A/G | 0.0298908 | 0.118541 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46406228 | ccggctaatttttgt[A/G]tttttagtagagaca | 55626 |
rs7925678 | snp | A/G | 0.489893 | 0.0703642 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46549309 | GTGTTATCCACTGTG[A/G]CATTGTTTCTTTAGC | 55626 |
rs7928869 | snp | G/T | 0.0298908 | 0.118541 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46407292 | CTCTCGCTGTCAGGG[G/T]TTACTGGGAGCTCTG | 55626 |
rs7930103 | snp | C/T | 0.289424 | 0.246872 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46462704 | ATGTTTACTAAAATC[C/T]CCTTCATCCCTCATC | 55626 |
rs7930857 | snp | A/G | 0.0887219 | 0.191022 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46425889 | tggtgtctcacgcct[A/G]taatcccagcacttt | 55626 |
rs7932866 | snp | A/G | 0.271972 | 0.249033 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46526544 | taaaaaaaaaattaa[A/G]attaaaaaaaaaaaa | 55626 |
rs7942262 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46523611 | TTCTTTTTATTAGCA[C/T]TAATGGCTATAATCT | 55626 |
rs7942614 | snp | C/T | 0.0916144 | 0.193427 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46428883 | GTAGGATGGCAGGCA[C/T]AATCTCTGGGGGCAG | 55626 |
rs7942788 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46423050 | AGGTTTTAGTGAGGG[C/T]TACTAGAAGAGAATC | 55626 |
rs7946071 | snp | A/G | 0.0422008 | 0.138995 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46429198 | CTCCCCCTCTCCCTC[A/G]GACAATCTTCGCCTA | 55626 |
rs7946705 | snp | A/G | 0.274393 | 0.248807 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46399608 | gacttcaggcgatcc[A/G]cccacctaggcctcc | 55626 |
rs7946801 | snp | A/G | 0.039522 | 0.134904 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46547722 | ATACAGTACTTCAGA[A/G]AGACTTTAGGGACTG | 55626 |
rs7949282 | snp | A/C | 0.490453 | 0.0684267 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46500756 | GCTATACCCATCACC[A/C]ATATCAATTCCTCTC | 55626 |
rs7949371 | snp | C/T | 0.490453 | 0.0684267 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46500754 | TCGCTATACCCATCA[C/T]CAATATCAATTCCTC | 55626 |
rs7951579 | snp | A/G | 0.438666 | 0.164028 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46448350 | aaacaatacatttct[A/G]aacaacacatggctc | 55626 |
rs7951713 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46418332 | TTTATATATAAATAT[A/G]TATTTTATTATTTAT | 55626 |
rs10160701 | snp | C/T | 0.375399 | 0.216275 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46530368 | CTAGCATGACCTGCA[C/T]TGGGAGAAGGGCTGC | 55626 |
rs10546476 | in-del | -/TA | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46418319 | ATATATTTTATTATT[-/TA]TATATAAATATGTAT | 55626 |
rs10636730 | in-del | -/TA | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46418344 | ATGTATTTTATTATT[-/TA]TATATAAATATATAT | 55626 |
rs10639461 | in-del | -/GAC | 0 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46401263 | CTCAGCTCTTTTCGA[-/GAC]GACAGAGTCTCGCTC | 55626 |
rs10680247 | in-del | -/CT | 0.438806 | 0.163867 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46399928 | CGGCTCAAATCTCAG[-/CT]CTGTCACTTGCTTGC | 55626 |
rs10734546 | snp | C/T | 0.0298908 | 0.118541 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46423845 | ATCAGCTCACCACAA[C/T]CTCTGCCTCCTGGGT | 55626 |
rs10742779 | snp | A/C | 0.0298908 | 0.118541 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46423877 | CAAGCGATTCTCCTG[A/C]CTCAGCCTCCCGAGT | 55626 |
rs10742780 | snp | A/T | 0.130694 | 0.219696 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46428103 | GCATATTGCTAGCGC[A/T]CTAGAGGGAGAAGGG | 55626 |
rs10769201 | snp | A/C | 0 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46519433 | TACTAAAAAATTATA[A/C]CCTGAAGATACTCTT | 55626 |
rs10838602 | snp | A/G | 0.283421 | 0.247756 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46502922 | AAAAATTAGCTGGGC[A/G]TGGTGGCAGGCACCT | 55626 |
rs10838603 | snp | A/C | 0.5 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46507008 | atctctactaaaaat[A/C]caaaaaaaaaaaaaa | 55626 |
rs11038887 | snp | C/T | 0.00394476 | 0.0442359 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46410695 | TGGGTCCTGAGTATT[C/T]TTCAGACACAGAGAA | 55626 |
rs11038889 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46410934 | tgtgaaaccctgtct[C/T]tactaaaaatacaaa | 55626 |
rs11038890 | snp | C/T | 0 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46416548 | AGGCCACTGACCTAA[C/T]TCAGCCGATAAGGAC | 55626 |
rs11038891 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46419355 | AAGACATGGGCTTTA[C/G]AGTTAATAAGACTTG | 55626 |
rs11038892 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46421223 | GGGTTGTTGCTAGCC[A/C]CTTCCCAACTTCTGC | 55626 |
rs11038893 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46422935 | CTAGAAGAGCTGTGG[A/G]AAAAGGTGCAAGGTG | 55626 |
rs11038894 | snp | C/G | 0.134802 | 0.221877 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46423115 | TGCTAAGAGACAGCT[C/G]ACCTTTCCATTGGAA | 55626 |
rs11038895 | snp | C/T | 0.305685 | 0.24372 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46425696 | AATACAGAAATTAGC[C/T]GGGGTGGTGGCATGC | 55626 |
rs11038897 | snp | C/T | 0.369958 | 0.21934 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46449277 | TGCCAGATGACATCA[C/T]TGTCTAATCCCAAAG | 55626 |
rs11038898 | snp | G/T | 0 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46468120 | ACACATTTGTTGAAT[G/T]AAGAAATGGCCAAAC | 55626 |
rs11038900 | snp | A/G | 0.375399 | 0.216275 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46473752 | GCCTCGCGGGTTCAC[A/G]CCATTCTCCTGCCTC | 55626 |
rs11038901 | snp | C/T | 0.0912534 | 0.193131 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46474339 | GGTATATGATCAATA[C/T]GAACAGGTCTATTCA | 55626 |
rs11038902 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46477844 | actttgggaggctga[A/G]acgggcagatcgctt | 55626 |
rs11038904 | snp | C/T | 0 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46487467 | CAAACAGAAGGATGC[C/T]TGAGAAAAGATTGTA | 55626 |
rs11038906 | snp | A/G | 0.324145 | 0.238752 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46514892 | AGATACAGAGTCTGG[A/G]AAAAAAGGAAAATCA | 55626 |
rs11038907 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46516654 | tagccaggatggtct[C/T]gatctcctgacctca | 55626 |
rs11038908 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46516669 | tgatctcctgacctc[A/G]tgatccgcccacctc | 55626 |
rs11038909 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46516685 | tgatccgcccacctc[A/G]gcctcccaaagtgct | 55626 |
rs11038910 | snp | C/T | 0.490063 | 0.0697833 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46521974 | GCTTTTCACCAGAAA[C/T]GCTTAAAAACATCTT | 55626 |
rs11038911 | snp | C/T | 0 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46536011 | CTTCCTTGTACAACT[C/T]TAAGTAATACCGTTT | 55626 |
rs11038913 | snp | C/T | 0.0670745 | 0.170406 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46538180 | GTGTACGCACTTATT[C/T]TACAACATACCTCAT | 55626 |
rs11038914 | snp | C/T | 0.370365 | 0.219117 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46539751 | tgacttgcatagagt[C/T]gttgttgaaggcaga | 55626 |
rs11038915 | snp | C/T | 0 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46547439 | TGTTAGGCAGTATAT[C/T]TACAAACAGAAATAT | 55626 |
rs11038916 | snp | A/G | 0.0916144 | 0.193427 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46550000 | ATTTTTGTATTTTTA[A/G]TAAAGACCAGGTTTT | 55626 |
rs11038917 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46550118 | GCTACTGCACCCAGC[C/T]GACACTAGCTTTTCT | 55626 |
rs11038919 | snp | A/G | 0.271972 | 0.249033 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46564231 | ATTAAAAAAAAAAAA[A/G]AGAGAAATCCCAGTA | 55626 |
rs11038921 | snp | A/T | 0 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46569442 | TTAAAAAAAAAAAAA[A/T]ATATATATATATATA | 55626 |
rs11038922 | snp | C/G | 0.101658 | 0.201233 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46572814 | AATAAGTATTCTGAG[C/G]TGGGTATGGTGGCTC | 55626 |
rs11038923 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46575727 | TCACCATATTGGCCA[A/G]GCTGGTCTCGAACTC | 55626 |
rs11038924 | snp | C/T | 0.0298908 | 0.118541 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46576301 | GAGACATTGGTGTTG[C/T]TGttgttttgtagac | 55626 |
rs11038927 | snp | C/G | 0.438526 | 0.164189 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46577698 | gctcatgcctataat[C/G]ccagcactttgggag | 55626 |
rs11038929 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46584384 | GTTGTGGGGTGGGGG[A/G]AGGGGGGAGGGATAG | 55626 |
rs11038930 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46584385 | TTGTGGGGTGGGGGG[A/G]GGGGGGAGGGATAGC | 55626 |
rs11038931 | snp | A/G | 0.0194156 | 0.0965963 | upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46595928 | aCTCTCCTTCTTGGA[A/G]AGGCTTGTGGAGCAT | 55626 |
rs11313362 | in-del | -/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46466923 | TTCTTTTCTTTTTTC[-/T]TTTTTTTTTTTTTGA | 55626 |
rs11337927 | in-del | -/A | 0.320814 | 0.239761 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46468815 | GTGAGGCTCCGTCTC[-/A]AAAAAAAAAAAAAGA | 55626 |
rs11386442 | in-del | -/A | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46445071 | ACAAAAAAAAAAAAA[-/A]CAAAAAAAAACTTAG | 55626 |
rs11393945 | in-del | -/A | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46579065 | AAAAAAAAAAAAAAA[-/A]GATAAGGAATGAACT | 55626 |
rs11449187 | in-del | -/T/TT/TTT | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46478648 | TTTTCTTTTTTCTCT[-/T/TT/TTT]TTTTTTTTTTTTTTT | 55626 |
rs11539337 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46428745 | GCTGTGCCACCTGGT[C/G]CCGACAAGAAAGCCG | 55626 |
rs11556617 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46428774 | AAGCTGACAGAGATA[C/T]CTACAGACGGAGTGC | 55626 |
rs11556618 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46428761 | TACCTACAGACGGAG[C/T]GCTGTGCCACCTGGT | 55626 |
rs11600177 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46564063 | gcaggagaatcgctt[C/G]aacccaggaggcaga | 55626 |
rs11600180 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46564075 | cttcaacccaggagg[C/T]agaggttgcagtgag | 55626 |
rs11600371 | snp | A/G | 0.00873346 | 0.0655016 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46514565 | tttcatcaattctaa[A/G]acacacttttcacct | 55626 |
rs11600659 | snp | C/G | 0.00943375 | 0.0680285 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46505494 | AAACAAGATTCTAGT[C/G]TACATCAGCCCAAAA | 55626 |
rs11601182 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46541039 | AAATTTCAGTTGCTT[C/T]GACAGAGGATGTAAT | 55626 |
rs11601978 | snp | A/G | 0 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46495197 | CTGGACAGAGCAGTT[A/G]ATGAGCGGCTTAACC | 55626 |
rs11604263 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46564076 | ttcaacccaggaggc[A/G]gaggttgcagtgagc | 55626 |
rs11604614 | snp | C/T | 0 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46481688 | CTCTGAAGGTAAAGC[C/T]TGAGATTAGATTTTA | 55626 |
rs11604628 | snp | C/T | 0 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46481774 | AAAgagcaggactgc[C/T]tgaggtccaactccc | 55626 |
rs11604750 | snp | A/C | 0.0178098 | 0.0926698 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46445084 | aacaaaaaaaaaaaa[A/C]caaaaaaaaacttag | 55626 |
rs11605029 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46558382 | agtgaaaccccagct[C/T]tactaaaaataccaa | 55626 |
rs11605325 | snp | A/C | 0 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46540848 | ctcaggtgggtaaag[A/C]ccatgtattatactt | 55626 |
rs11605821 | snp | A/C/T | 0.5 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46429327 | GGGGAGGAGCAGCCG[A/C/T]TAAGGTGGCAGGATA | 55626 |
rs11607060 | snp | C/T | 0.444444 | 0.157135 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46411807 | ttttattttttattg[C/T]ttgaggtggggtctc | 55626 |
rs11819869 | snp | C/T | 0.3752 | 0.216391 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46539130 | TAGATTAAAGAAAGC[C/T]AGCCAAGCATTGATA | 55626 |
rs11820385 | snp | C/T | 0 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46545502 | GGATGACAACTTGCC[C/T]TGAGCAGGGATAACA | 55626 |
rs11821531 | snp | A/G | 0.105569 | 0.204058 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46458838 | TACACAAGGAATGTC[A/G]CCATTGGCCTTAGAA | 55626 |
rs11821839 | snp | A/C | 0.0146672 | 0.084371 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46416974 | AAGGGGAAGGGGTGT[A/C]ATCAGGACTTCAGAC | 55626 |
rs11821877 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46477175 | GGTGGAAGGGTGGGA[A/G]GGGAAAGGGACCCAG | 55626 |
rs11822248 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46538699 | gacgcggttttacca[C/T]gttagccaggctggt | 55626 |
rs11824513 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46511256 | CCTTATATTTAGGGT[A/G]TATAATCCTCAAACA | 55626 |
rs11825765 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46419488 | AAATGCCTGCCATGG[G/T]GCAAGCTCCTAAATA | 55626 |
rs11826454 | snp | A/C | 0.0037807 | 0.0433135 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46506810 | AGGATGGAAAGAAAC[A/C]CAATGAATGGCTAGA | 55626 |
rs11826518 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46534530 | AGCACCTGAAATCCA[A/G]CAGGTGCTTGGTAAA | 55626 |
rs11827944 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46487527 | ggtttgtaatacata[C/T]agatgtaatattaat | 55626 |
rs11828360 | snp | A/G | 0 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46419535 | CAACCAGGAACCTGT[A/G]TCTCAGTCTCTTCAC | 55626 |
rs12099188 | snp | A/C | 0.030278 | 0.119257 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46551975 | ggaggttgtagtgag[A/C]caagatcgcaccact | 55626 |
rs12099394 | snp | A/T | 0.0189856 | 0.0955633 | intron-variant, upstream-variant-2KB | AMBRA1, MIR3160-2 | GRCh38.p7 | 11:46450218 | catccatacaatgga[A/T]tattattcatgctaa | 55626 |
rs12221816 | snp | C/T | 0 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46415284 | CTCTCTCATTTCCAC[C/T]TGCATCCATGCCTGA | 55626 |
rs12226785 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46492910 | aaaaattagctgggc[A/G]tggtggcgggcacct | 55626 |
rs12271359 | snp | C/G | 0 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46514820 | AACACATAAAATAAC[C/G]GCATGTCTTTGAGTC | 55626 |
rs12272795 | snp | A/G | 0.275999 | 0.248644 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46522522 | GACCAAATCTATGGG[A/G]AAAAAAAAGGTCCAC | 55626 |
rs12273343 | snp | C/G | 0.0887219 | 0.191022 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46576246 | TCTCTATTGATTACT[C/G]CTTTGTGAGAAAAGT | 55626 |
rs12277441 | snp | A/G | 0 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46477781 | AAGGAAGTCCTAAAA[A/G]ATTGATTGGTGAggc | 55626 |
rs12277858 | snp | C/T | 0.0850919 | 0.187897 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46463599 | AATTACAACTCAATT[C/T]GTTAACTAGGACTCA | 55626 |
rs12278633 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46578771 | ctgtagtcccagcta[C/T]tcaggaggctgaggc | 55626 |
rs12278857 | snp | A/C/T | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46570106 | tcgctactaaaaata[A/C/T]aaaaaaatagctggg | 55626 |
rs12280028 | snp | A/G | 0.133777 | 0.221342 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46554610 | CTGTTGCTTTAAAAG[A/G]ATAAGGGACTTCTCT | 55626 |
rs12280656 | snp | C/T | 0.134119 | 0.221521 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46485051 | caagcgattctcctg[C/T]cttggcctcccgaat | 55626 |
rs12280708 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46455028 | gggaccacaggtgta[C/T]gccaccccacaccca | 55626 |
rs12283172 | snp | C/T | 0.282895 | 0.247826 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46420976 | TAAAAGACCTCTTTC[C/T]TAGAAATGTTCCAGA | 55626 |
rs12285637 | snp | C/T | 0.0832709 | 0.186283 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46578834 | tgcagtgagccgaga[C/T]tgcaccactgcatgc | 55626 |
rs12287515 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46549825 | CTTTTCTTTCTTTTT[G/T]GGGGGGGGTGGggga | 55626 |
rs12287998 | snp | C/T | 0.0722614 | 0.17581 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46553844 | GAAACAAATTCTAGC[C/T]TGTATCCTCATGATA | 55626 |
rs12288189 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46428838 | CCAGACCTTTAGGCC[A/G]AGGCCTGCCAGTCTC | 55626 |
rs12290327 | snp | A/G | 0.0919752 | 0.193722 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46490477 | TCTATAGTAGCTTCT[A/G]TTTTCTATTATTGCT | 55626 |
rs12290779 | snp | A/C | 0.133093 | 0.220981 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46573421 | aaaaacaaaacaaaa[A/C]aaaaaaaaCTCAGTC | 55626 |
rs12295266 | snp | A/T | 0.27278 | 0.24896 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46586404 | TCTCCAAAAAATAAT[A/T]AAAAAATAATTTTTT | 55626 |
rs12295608 | snp | A/G | 0.0407846 | 0.136854 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46397861 | CTCCCGCTGCACCAC[A/G]GCTGTCATGCCGCCC | 55626 |
rs12362679 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46409005 | GAGTGGGGAGGAGCT[A/G]TAGAGATGGCTGATC | 55626 |
rs12363193 | snp | C/G | 0 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46526387 | aatcaagagaatgca[C/G]caagctgtgccaatt | 55626 |
rs12364818 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46529727 | TTTCAACAGAATCCA[C/G]ATACCCGAATTGATA | 55626 |
rs12418809 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46497148 | taaaataaaataaaa[A/T]aaTAAAGGGAAGGgg | 55626 |
rs12420739 | snp | A/G | | | upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46595352 | gaccagcctggtcaa[A/G]atggtgaaaccccgt | 55626 |
rs12420810 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46520770 | ccggctaattttttg[G/T]atttttttttttttt | 55626 |
rs12573925 | snp | C/T | 0.105924 | 0.204309 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46569381 | TATAACACACATTAC[C/T]CTGCAGCCTACCTTT | 55626 |
rs12573978 | snp | A/G | 0.283947 | 0.247685 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46556850 | AGTATGAAAATGGTA[A/G]TAAGggctggttgcg | 55626 |
rs12574147 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46545164 | aaaaaaaaaaGCCGG[C/G]GGGGGGGGGGTGGTG | 55626 |
rs12574250 | snp | A/G | 0.202343 | 0.245416 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46469609 | GCACAATTTAAATAT[A/G]TTATCTTCAGAGTAA | 55626 |
rs12574668 | snp | A/C | 0.325799 | 0.238232 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46401136 | GCCCCAATGCTTTCT[A/C]AGAACTCTGTGCACT | 55626 |
rs12575938 | snp | G/T | 0.0312421 | 0.121016 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46580910 | gatcctcccacctta[G/T]cctcttgagtagctg | 55626 |
rs12576204 | snp | C/T | 0.0198 | 0.0975088 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46527091 | AGGCTCTCCATCTTT[C/T]TGAAACACATTTCAG | 55626 |
rs12576317 | snp | A/G | 0.203267 | 0.245593 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46552226 | atacaaaaattagcc[A/G]ggcgtggtggtgcac | 55626 |
rs12576359 | snp | G/T | 0.283421 | 0.247756 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46502839 | GCCGAAGTGGGCAGA[G/T]CACGAGGTCAGGAGT | 55626 |
rs12577441 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46461328 | GCAAAATGTCAATAA[C/T]TATTAAATTTTGGTT | 55626 |
rs12577889 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46585692 | aaaaaaaaaaaaaaa[A/G]aaaatatatatatat | 55626 |
rs12578042 | snp | C/G | 0.3742 | 0.216966 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46493454 | GCCATTTCCTGCCTT[C/G]AAGTAAGGAACTGAA | 55626 |
rs12789427 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46527313 | agcaagaccccatct[C/T]tactaaaaatacaaa | 55626 |
rs12789485 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46527440 | agccgagatcatgcc[A/C]ctgtattccagccta | 55626 |
rs12789520 | snp | A/G | 0 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46527504 | aaaaaaaaaaaaaaa[A/G]ggcaacctatggaat | 55626 |
rs12789976 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46527469 | taggtgacaaagtga[C/G]actgtctcaaaaaaa | 55626 |
rs12793320 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46578713 | acggtgaaaccctct[C/T]tactaaaaatagaaa | 55626 |
rs12795616 | snp | A/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46573855 | agagtgtgatattcc[A/C]cttcctgtgtccatg | 55626 |
rs12799001 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46505756 | atcgagggggaagga[A/G]ggggagagagagagg | 55626 |
rs12799434 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46400509 | ttttttttttttttt[G/T]gagaccaggtctcgc | 55626 |
rs12799895 | snp | C/G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46466899 | ctaaaattactaatg[C/G/T]ttctttttttctttt | 55626 |
rs12806954 | snp | A/T | | | upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46595256 | tttttttttttttaa[A/T]tgccgggcgcagtgg | 55626 |
rs12807530 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46520898 | gcgtgagccaccgcg[C/G]ccggccCCTATAGCA | 55626 |
rs12808447 | snp | G/T | | | upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46595257 | ttttttttttttaaa[G/T]gccgggcgcagtggc | 55626 |
rs12809036 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46471626 | AAATAACtttctttc[A/T]gttttgttttgtttt | 55626 |
rs16938506 | snp | A/C | 0.375 | 0.216506 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46432763 | TTCACAGGTTCTTGG[A/C]TTCTGACAAAGCTTG | 55626 |
rs16938510 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46475060 | TGAGGTGAATTGAAT[A/G]TATCTTAAACTGAAA | 55626 |
rs17004881 | snp | A/G | 0.1302 | 0.219426 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46428775 | GAAGCTGACAGAGAT[A/G]CCTACAGACGGAGTG | 55626 |
rs17196997 | snp | A/C | 0.0325976 | 0.123435 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46427492 | GATGGAATCGCCCTA[A/C]AGCCCATGGTTCGTT | 55626 |
rs17197116 | snp | C/T | 0.138546 | 0.223781 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46498752 | TGACTTGGGCCTTTA[C/T]AAATGAAGCTCTTGC | 55626 |
rs17725808 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46422908 | GAGGAAGCGGACAAC[C/T]GGAAACTGAGGCTAG | 55626 |
rs17787739 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant, downstream-variant-500B | AMBRA1 | GRCh38.p7 | 11:46430713 | TGTTCTCCTGGGAAT[A/G]TCTGTTGGCCCAACA | 55626 |
rs17787804 | snp | C/T | 0.489376 | 0.0721049 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46485335 | TGCCCCACTTACTCA[C/T]GCTTATAGTCCCACT | 55626 |
rs17854361 | snp | C/T | 1.65438e-05 | 0.00287605 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46548279 | CCACCGGGTTTTATC[C/T]TCTACCAGCTCCTGC | 55626 |
rs28366016 | snp | C/T | 0.0107246 | 0.0724382 | upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46594659 | ACCCAAAGAGACTTT[C/T]GCTTATTATGTAAGA | 55626 |
rs28366017 | snp | A/C | 0.0663309 | 0.169604 | upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46594479 | TTTACGTAGACTGTT[A/C]ATTTTGTTCCTCAGC | 55626 |
rs28366018 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46594230 | CTTTAACAGCCGGCG[A/G]CCCACAGAAAATGGC | 55626 |
rs28502617 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46470443 | AAATACAAAAAATTA[C/G]CCGGGCGTGGTGGTG | 55626 |
rs28579019 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46418325 | TTTATTATTTATATA[A/T]AAATATGTATTTTAT | 55626 |
rs34032253 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46481874 | GTAAAAATGACAGTG[A/T]ATCATAGCAATGCTG | 55626 |
rs34040432 | in-del | -/T | 0 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46439925 | ATGCCCACATACTAC[-/T]TTTTTTTTTTAACAT | 55626 |
rs34070050 | in-del | -/A/AC/ACACACACACACACACACACAC/CACAC | 0.5 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46419995 | GCACGTGTCCTCAAT[lengthTooLong]CACACACACACACAC | 55626 |
rs34092566 | in-del | -/T | 0.00199481 | 0.0315187 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46510980 | AGGAAAAATACTTCC[-/T]TTTCCAAAAAAACCT | 55626 |
rs34105140 | in-del | -/A | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46475217 | TATAACTTGGAATGC[-/A]AAAGTATTAATTATG | 55626 |
rs34121527 | in-del | -/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46556904 | ACCTTGGGAGGCTGA[-/G]GGCGGGTGGATCACC | 55626 |
rs34127583 | in-del | -/A | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46405571 | AAAAAAATAATGATT[-/A]AAAAAATAGCCAGGC | 55626 |
rs34148812 | in-del | -/A | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46526735 | ACACACAAAAAAAAA[-/A]CCATGAAAAATAACT | 55626 |
rs34171336 | in-del | -/T | 0 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46514641 | GTTTAATTGGCAGGA[-/T]TTTTTTTTTTTTTGA | 55626 |
rs34202792 | in-del | -/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46593619 | CTAAAGAACCACACC[-/G]GGGAAGCCCCAGCAA | 55626 |
rs34217002 | snp | C/T | 0.0298908 | 0.118541 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46500624 | CTGATATCTCTCTCA[C/T]ATCACAAACACTCCA | 55626 |
rs34219076 | in-del | -/A | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46419997 | ACGTGTCCTCAATAC[-/A]CACACACACACACAC | 55626 |
rs34245698 | in-del | -/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46468668 | AAAAAAAAAATAGCC[-/C]GGGTGTGGTGGCGGG | 55626 |
rs34329058 | in-del | -/A | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46485774 | ATATAAAAGGAACAG[-/A]AAAAGTTCATTGACA | 55626 |
rs34329341 | in-del | -/G | | | frameshift-variant, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542783 | TCCTGTCAACCCAGG[-/G]AGCTATTTCTCGGTG | 55626 |
rs34394292 | in-del | -/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46440519 | ATTTTTTAAATTTTT[-/G]GAACAGTAATATCAA | 55626 |
rs34444424 | snp | C/T | 0.0298908 | 0.118541 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46457225 | AATTCAAAGCCTGCT[C/T]CATTCAGGCTAAGGA | 55626 |
rs34445491 | snp | C/G | 0.0410537 | 0.137264 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46402430 | GCGGTGGCGAGATCT[C/G]AGCTCACTACAACCT | 55626 |
rs34446488 | in-del | -/A | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46490384 | GAATAATAGACTATC[-/A]AAAACACTTTTCTCT | 55626 |
rs34457629 | in-del | -/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46431737 | AAAGCAGAGACCAGC[-/T]TTCTGCTTAAGAGAA | 55626 |
rs34466906 | in-del | -/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46444362 | GTATGACATTTTTTT[-/C]CCTTGGTAACCAATT | 55626 |
rs34485813 | in-del | -/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46417184 | GCCTCCTGAGTAGCT[-/G]GGGACTACAGGCACG | 55626 |
rs34485908 | in-del | -/G | | | upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46594341 | CCCCAACTGTTCTAT[-/G]GGACTCCCAACACTC | 55626 |
rs34486418 | snp | A/G | 0.5 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46520425 | TTCTAGCTAAACTAA[A/G]CACACCCTCACTATC | 55626 |
rs34535902 | in-del | -/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46506923 | TTATCCCAGCACTTT[-/G]GGGAGGCCAAGGCAG | 55626 |
rs34538699 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46579044 | GACCACAAGAAAGCA[A/T]TAAAAAAAAAAAAAA | 55626 |
rs34540155 | in-del | -/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46428590 | CTTCTTCTTCTTCTT[-/T]CTTTTTTTTTTAAGG | 55626 |
rs34571249 | in-del | -/G | | | downstream-variant-500B | AMBRA1 | GRCh38.p7 | 11:46396365 | CCCTCACTTCCCAAT[-/G]CCCCACCCCTCCCCC | 55626 |
rs34595875 | in-del | -/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46564536 | TGTATAGTGCTCTAA[-/C]CCATTATACAATACT | 55626 |
rs34674110 | in-del | -/G | | | utr-variant-5-prime, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46548496 | AAGTTGTCCTCATGG[-/G]AAATCTTAAGGAACA | 55626 |
rs34682193 | in-del | -/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46422007 | CCTGAAGCTCCCCAT[-/G]GGGATGTTCAGAACA | 55626 |
rs34694924 | in-del | -/A | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46516795 | GGGAAATGGTAGGAG[-/A]AAAATTGAATGCGAT | 55626 |
rs34740424 | in-del | -/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46515269 | CTGAGCTCAGGAGTT[-/C]CAAGACCAGCCTGGG | 55626 |
rs34770512 | snp | A/G | 0.0232847 | 0.105357 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46522627 | AGGCAGTGTATCCTA[A/G]TTCACTGATTTCCCC | 55626 |
rs34770824 | snp | C/T | | | intron-variant, upstream-variant-2KB | AMBRA1, MIR3160-2 | GRCh38.p7 | 11:46450032 | CCACTGCACTCCAGC[C/T]TGGGCAACAGAGCGA | 55626 |
rs34777348 | snp | C/T | 0.5 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46516424 | AAAGAAAGATCTTTC[C/T]TTTTTTTTTTTTTTT | 55626 |
rs34785738 | in-del | -/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46469857 | TTTTTTTTTTTTTTT[-/T]GGTAGAGATATGGTC | 55626 |
rs34797569 | in-del | -/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46462878 | TGCTTCAAAACTCCC[-/C]AAGTAGCTGGGATTA | 55626 |
rs34824728 | in-del | -/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46547601 | ATTGAGAAACTTTCC[-/C]AAGTTTTGATCCTCT | 55626 |
rs34840317 | in-del | -/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46420241 | GAATTCGTTAAGGCT[-/C]CCTTAAATCTTTGCT | 55626 |
rs34874765 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46543857 | CTAGCTTTAAATCTT[A/G]ACTGGAAAGATAAGA | 55626 |
rs34935608 | in-del | -/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46497022 | AGGTTAAGACACAAG[-/T]AATCGCTTGAACCAG | 55626 |
rs34937038 | in-del | -/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46553493 | GCTCACACCTGTAAT[-/C]CCCAGCACTTTGGGA | 55626 |
rs34958070 | in-del | -/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46404074 | GCCAGGCGTGGTGGC[-/T]GTGTGCCAGGAGGCT | 55626 |
rs34988876 | in-del | -/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46492459 | GATTCTCCAAAACAG[-/T]AATGTCATTTTAAAA | 55626 |
rs35002067 | in-del | -/A | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46432965 | CGTGCCTTAGACAAG[-/A]ACAGGGTCCTAGACA | 55626 |
rs35012433 | in-del | -/A | 0 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46585385 | ATTCCAAAAAAAAAA[-/A]CGCTGGGCATGGTGC | 55626 |
rs35066434 | in-del | -/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46557779 | TGCCACCACACTCCA[-/G]CCTGGGTGACAGAGC | 55626 |
rs35074925 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46564472 | GGCTAAATGATTTAC[C/T]TAAGTGAAGGAGAGA | 55626 |
rs35080820 | in-del | -/A | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46499758 | CCTCCTGTGTTCAAG[-/A]CAATTCTCTGCCTCA | 55626 |
rs35088330 | in-del | -/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46484777 | GCCTCCCGAGTAGCT[-/G]GGGACTACAGGCACC | 55626 |
rs35148999 | in-del | -/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46414839 | TCCTAAGAATTCCTT[-/T]CCCCTGGAGAGATGG | 55626 |
rs35182301 | in-del | -/A | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46410841 | CGCCAGTGGCTCACG[-/A]CCTGTAATCCCAGCA | 55626 |
rs35196145 | in-del | -/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46441041 | TGCCTGATTCACTAC[-/T]TTTTTGCTAACAATC | 55626 |
rs35198694 | in-del | -/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46462837 | CTCACTGCAACCTCC[-/C]GCCTCCCAGGTTCAA | 55626 |
rs35213610 | in-del | -/A | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46520158 | AAAAAAAAAAAAAAA[-/A]TTACGAGGCTCCTAA | 55626 |
rs35217088 | in-del | -/A | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46503088 | AAAAAAAAAAAAAAA[-/A]TGAATTTTTGCTTTG | 55626 |
rs35234634 | snp | C/G | 0.0236746 | 0.106192 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46428851 | CCGAGGCCTGCCAGT[C/G]TCTGGACGGCTACGG | 55626 |
rs35235882 | in-del | -/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46474765 | GGATTAGTACTCATT[-/G]CTGGATTTTCCCTAT | 55626 |
rs35254574 | in-del | -/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46560373 | CTGTAACTATAATAA[-/G]GGGGGGAGAAGTGAA | 55626 |
rs35266625 | snp | C/T | 0.444444 | 0.157135 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46513171 | ACAGAGATTATCACA[C/T]AGTGCTAACATTTAT | 55626 |
rs35307902 | in-del | -/A | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46528940 | CAGAAGAGGCAAAAA[-/A]GAGTCACACGTACCC | 55626 |
rs35310801 | in-del | -/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46488153 | TCACAAAATACATTA[-/C]ATCAAAAATTGACAA | 55626 |
rs35327580 | snp | A/G | 0.317933 | 0.240593 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46584267 | TCTCAGTAAACTATC[A/G]CAAGGACAAAAAACC | 55626 |
rs35357993 | in-del | -/A | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46559299 | TCTCAAAAAAAAAAA[-/A]GAAAGAAAAGAAAAG | 55626 |
rs35385447 | snp | G/T | 0.00795532 | 0.062565 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46415414 | TGGAAGACTGTACAT[G/T]GCTTTCGTCAGAATT | 55626 |
rs35396289 | in-del | -/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46440505 | TATTAATCTTTTATA[-/T]TTTTTTAAATTTTTG | 55626 |
rs35398258 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46565887 | AAGTGATCCTCCCAC[C/T]TCAGCCACCCAAGTA | 55626 |
rs35415731 | in-del | -/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46562804 | ATGCAACATTGGTTC[-/T]TTTTTTTTTTTTTGA | 55626 |
rs35448540 | in-del | -/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46498089 | ATAGAAGGAGACAAA[-/T]TTTGGTCAGGCAGGC | 55626 |
rs35465113 | in-del | -/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46506937 | TGGGAGGCCAAGGCA[-/G]GGCGGATCACAAGGT | 55626 |
rs35469009 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46477496 | AAGCTCAGCTAATTT[C/T]TGGAAAAAAAAAAAA | 55626 |
rs35495492 | in-del | -/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46437825 | AAGGTAGAGAGAAAA[-/G]GGGAGAAGTAAAATA | 55626 |
rs35505602 | in-del | -/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46535517 | CACAGAAACTTAAAG[-/C]AAAAAGCATCAGTAG | 55626 |
rs35526655 | in-del | -/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46437578 | ATTCTCACATTTGCT[-/G]GTTTGTTGTCTATTA | 55626 |
rs35538170 | in-del | -/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46403018 | CAGGCACAGTGGCAG[-/T]ACAGGGGGTTAATTC | 55626 |
rs35587166 | in-del | -/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46522753 | CTACGAAGAATATCC[-/C]TGGTAGAATCATTTA | 55626 |
rs35599081 | in-del | -/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46484547 | GCCTCAATCCAGACA[-/T]TATGGACATTAAGAT | 55626 |
rs35622606 | in-del | -/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46484975 | AAATCTCACTCTTGT[-/G]CCCCCAGGCTGGAGT | 55626 |
rs35623807 | in-del | -/C | | | frameshift-variant, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542653 | CCTGAGAGCCACCTT[-/C]CCTGCTGTCTCAGCA | 55626 |
rs35624125 | in-del | -/A | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46572808 | TTAAAAATAAGTATT[-/A]CTGAGCTGGGTATGG | 55626 |
rs35639064 | in-del | -/A | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46521216 | CAAGGTTTTCAGAAA[-/A]CTGCTTACATCACCT | 55626 |
rs35650286 | in-del | -/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46585111 | TAAATGGATTAAGGG[-/G]CGGTGCAAGATGTGC | 55626 |
rs35656227 | in-del | -/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46495991 | CACAGTGGTGTGCAT[-/G]CTGTAGTCTCAGTTA | 55626 |
rs35662565 | in-del | -/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46419998 | CGTGTCCTCAATACA[-/C]ACACACACACACACA | 55626 |
rs35677037 | in-del | -/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46510541 | TACACTTACTTTATA[-/G]GGCTACCCTAAGTAA | 55626 |
rs35703280 | in-del | -/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46546053 | TTTTTTTTTTTTTTT[-/T]GACAGGGGGTTTCAT | 55626 |
rs35715394 | snp | A/G/T | 0.0298908 | 0.118541 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46436291 | ATGTGATCTGATACT[A/G/T]AAGAGTGATTTGTAA | 55626 |
rs35734487 | in-del | -/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46523844 | CCCACTGACAGTTCC[-/C]TTGTGAGATGTCATA | 55626 |
rs35815676 | in-del | -/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46436934 | TCTATGGGCTTTAAG[-/T]ACAGCTTTGAACAGT | 55626 |
rs35841266 | in-del | -/A | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46405554 | TGAGACCCTATCTCT[-/A]AAAAAAAATAATGAT | 55626 |
rs35851912 | in-del | -/A | | | frameshift-variant, intron-variant | AMBRA1 | GRCh38.p7 | 11:46433613 | GGGACAGGCTCACCG[-/A]AAATGGCATTGGGAC | 55626 |
rs35866058 | in-del | -/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46526495 | TGCTATGTAAGAAGT[-/G]CTGCTATCCCTGTCA | 55626 |
rs35880540 | in-del | -/A | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46463258 | GGGCCAACTCAAAAT[-/A]CTACAAGCCAAGTAT | 55626 |
rs35892223 | in-del | -/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46436463 | GGACCACAAGGATGG[-/G]TTCTGTTTGCTAACT | 55626 |
rs35895608 | in-del | -/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46436457 | GAAGAGGGACCACAA[-/G]GGATGGTTCTGTTTG | 55626 |
rs35935319 | snp | C/T | 0.0298908 | 0.118541 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46441012 | TAATGTACTACAAGG[C/T]TTGGTGCAATGCCCT | 55626 |
rs35957462 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46415626 | CTTACATTTTGGGCC[C/T]TAAGGCTTGAGGCAT | 55626 |
rs35974067 | in-del | -/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46459099 | CCAACTACACCATGG[-/G]AACACCACGCAGCCA | 55626 |
rs35977174 | in-del | -/C | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46478807 | TACAGGCATGCACCA[-/C]CCATGCCCGAAGATA | 55626 |
rs35978491 | in-del | -/A | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46506498 | TTTCTTAAACACACT[-/A]AAAAGCTTTGTTGCA | 55626 |
rs35987296 | in-del | -/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46520786 | ATTTTTTTTTTTTTT[-/T]AGTAGAGACGGGGTT | 55626 |
rs36026838 | in-del | -/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46486474 | AATAAGGCTAATTCC[-/T]TAAAAGTTAGCAAGC | 55626 |
rs36105565 | in-del | -/A | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46573115 | CAAAAAAAAAAAAAA[-/A]GGATTCTGGCCAGGC | 55626 |
rs41530551 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46443844 | GTTGGCACTAAGTAA[A/G]TGTTAAGTAACAATG | 55626 |
rs55708034 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46539401 | CGTCTCTACTAAAAA[A/T]ACAAAATTAGCCAGG | 55626 |
rs55713914 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46556733 | CCATAAAATGTGACT[A/G]TTGATAGTATGTATA | 55626 |
rs55737385 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46590974 | TTCTATCACAAAGCA[C/T]GAGATAAGTTGATTA | 55626 |
rs55750336 | snp | C/T | 0.101301 | 0.200969 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46478978 | CCAAGGTGGTAGGAT[C/T]GCTTGAGCCCAAGAG | 55626 |
rs55806144 | snp | C/G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46595515 | GCACTCCAGCCTGGG[C/G/T]GACACAGCAAGACTC | 55626 |
rs55893883 | snp | A/G | | | intron-variant, upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46592399 | TTTAAATATCTCAAT[A/G]TTTGAATGATTTCTA | 55626 |
rs55933019 | snp | C/T | | | upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46595216 | GCACTCCAGCCTGAT[C/T]TATGGAGCAAGACCC | 55626 |
rs55971594 | snp | A/G | 0.0252325 | 0.109451 | intron-variant, upstream-variant-2KB | AMBRA1, MIR3160-1 | GRCh38.p7 | 11:46453413 | TGGGATTACAGGCAC[A/G]AGCCACTCTGCCTGG | 55626 |
rs56090695 | in-del | -/A | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46552405 | AAAAAAAAAAAAAAA[-/A]GGCCAGGCACGGTAG | 55626 |
rs56218032 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46582906 | CAAGAAATAGTTGTA[A/G]AAGGCCTCACAGGGA | 55626 |
rs56351820 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46587456 | TATCCTTGACTATGT[A/G]AAACCCAGTATTATC | 55626 |
rs56374939 | in-del | -/AC | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46459775 | CACACACACACACAC[-/AC]CCTGGAATACCACAG | 55626 |
rs56393748 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46520226 | TAATTTCAATTTATT[G/T]AAATTAAAACTGAAA | 55626 |
rs56680261 | in-del | -/GTGT | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46425351 | TGTGTGTGTGTGTGT[-/GTGT]AAGAAGTAGTATTTC | 55626 |
rs56707027 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46560824 | AAAAAAGAGTAGCTT[C/T]TGATGGAAGAAATTT | 55626 |
rs56834227 | in-del | -/AATAAATAAATA | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46486944 | ATAAATAAATAAATA[-/AATAAATAAATA]CAAATAAAAGAGATG | 55626 |
rs56851661 | snp | C/G | 0.0391387 | 0.134304 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46482762 | ACGCCTGTAATCCCA[C/G]CACTTTGGGGTGCCG | 55626 |
rs56977210 | snp | C/T | 0.146985 | 0.227789 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46507321 | CATCTCTACTAAAAA[C/T]ACAAAAAATTAGCCA | 55626 |
rs57084695 | in-del | -/TTTT | 0 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46551311 | GTTTGTGGGGACTTT[-/TTTT]ATTTTTATTTTTTAA | 55626 |
rs57125514 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46585940 | CCTCCCGAGTAGCTG[A/G]GATTACAGGCATGCA | 55626 |
rs57293525 | in-del | -/A | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46551115 | AAAAAAAAAAAAAAA[-/A]GAATAGATGTCCAAA | 55626 |
rs57342507 | in-del | -/GTGTGTGTGT | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46425342 | TGTGTGTGTGTGTGT[-/GTGTGTGTGT]AAGAAGTAGTATTTC | 55626 |
rs57416658 | snp | A/C/G | 0.0298908 | 0.118541 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46445384 | GTGTGCTGTCAGTGA[A/C/G]TCCACTGACCTCAAA | 55626 |
rs57535407 | snp | C/T | 0.284209 | 0.247648 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46548736 | AGTGGCTCACGCCTG[C/T]AATCCCCGAACTTTG | 55626 |
rs57618324 | in-del | -/A | 0.499 | 0.0223418 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46428031 | AAAAAAAAAAAAAAA[-/A]GTAACAAATATGCTT | 55626 |
rs57739175 | in-del | -/A | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46507496 | AAAAAAAAAAAAAAA[-/A]GATTGGCTAGCTTAA | 55626 |
rs57770866 | in-del | -/GA | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46531256 | AGTAATTGCAACAGA[-/GA]CTGTACAGCCTCCAA | 55626 |
rs57923752 | snp | A/G | 0.0298908 | 0.118541 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46577679 | AATTCAGCCAGGCGC[A/G]GTGGCTCATGCCTAT | 55626 |
rs58031860 | snp | C/T | 0.039522 | 0.134904 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46575839 | TTTTTCCAGGCACCA[C/T]AAACCAAAAATACAT | 55626 |
rs58147945 | snp | C/G | 0.312837 | 0.241974 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46479104 | CTGGGAGGCTGAGGC[C/G]GGGGAATCACTTGAG | 55626 |
rs58153579 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46557134 | AGAGCGAAACTCCAT[C/T]TCAAAAAAAAAAAAA | 55626 |
rs58157675 | in-del | -/CTT | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46585981 | AGCTAATTTGTATTT[-/CTT]TTAGCAGAGACAGGG | 55626 |
rs58254271 | in-del | -/A | | | upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46595900 | AAAAAAAAAAAAAAA[-/A]GAAAGAAAGAAAACT | 55626 |
rs58268270 | in-del | -/A | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46547899 | CAAAAAAAAAAAAAA[-/A]GTTAAAATACATGAT | 55626 |
rs58314136 | snp | G/T | 0.0314385 | 0.121371 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46466142 | TGTACTTCTTGCTTG[G/T]TTGGAGCCTACAATC | 55626 |
rs58634563 | snp | A/G | 0.0352966 | 0.128072 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46571239 | GAAGTTTGCCAGCTC[A/G]AGTCAGCACAAAGCT | 55626 |
rs58671092 | in-del | -/A | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46447252 | CGCAAAAAAAAAAAA[-/A]GGCCACGCGCAGTAG | 55626 |
rs58748629 | in-del | -/A | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46558574 | AAAAAAAAAAAAAAA[-/A]CCACTACCTACCTAG | 55626 |
rs58770070 | snp | A/C | 0.0298908 | 0.118541 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46510091 | GAATTCCCAAGCAGA[A/C]CAGCTAACAATCTTT | 55626 |
rs59044666 | in-del | -/ATAGATAGATAG | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46447768 | TAGATAGATAGATAG[-/ATAGATAGATAG]TGATGGCAAATACTA | 55626 |
rs59100978 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46586011 | GTTTCTCCACGTTGG[C/T]CAGGCTGGTCATGAA | 55626 |
rs59144630 | snp | A/G | 0.0919752 | 0.193722 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46536306 | AAAGGTAAACAAATA[A/G]TTTTCTGTCATGGGT | 55626 |
rs59261804 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46496682 | CAAGAAGACAACAGA[A/G]AAAAAGGGGCAAACC | 55626 |
rs59352642 | snp | C/T | 0.0271762 | 0.113356 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46560346 | AGATACAAAACTGAG[C/T]AAATTCTAATTACTG | 55626 |
rs59366507 | snp | A/G | 0.0267878 | 0.112589 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46503445 | TACAATTGATCACAG[A/G]TCACCATAACAGATC | 55626 |
rs59385965 | in-del | -/A | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46507177 | CAAGACTCCGTCTCA[-/A]AAAAAAAAAAAAAAA | 55626 |
rs59454111 | snp | A/G | 0.146314 | 0.227484 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46519077 | CACCCAGGCTGGAGT[A/G]CAGTGGCGCGATCTT | 55626 |
rs59488332 | snp | A/G | 0.030278 | 0.119257 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46559451 | ATCACTACCTCAACT[A/G]TAAGTAGGGAAGAAG | 55626 |
rs59510298 | in-del | -/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46545174 | GCCGGGGGGGGGGGG[-/G]TGGTGGTGGGCATGG | 55626 |
rs59531129 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46571814 | CCTGCCTCAGCCTCC[C/T]GAGTAGCTGGGACTA | 55626 |
rs59598381 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46585986 | AATTTGTATTTTTAG[C/T]AGAGACAGGGTTTCT | 55626 |
rs59598480 | in-del | -/TTCT | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46413492 | GCTTTCTTTCTTTCT[-/TTCT]CTATTTTTTTCTGAG | 55626 |
rs59649866 | snp | C/T | 0.146314 | 0.227484 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46484224 | ACTGGAAAATATGGG[C/T]TTTGACCTCACATTT | 55626 |
rs59664414 | snp | C/G | 0.0298908 | 0.118541 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46551357 | TCACTCTATCACCCA[C/G]GCTGGAGTGCGATGG | 55626 |
rs59903160 | in-del | -/A | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46411114 | CAAAAAAAAAAAAAA[-/A]GAAAAAAAAAAAAAA | 55626 |
rs59904013 | in-del | -/A | 0 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46527504 | AAAAAAAAAAAAAAA[-/A]GGCAACCTATGGAAT | 55626 |
rs59930897 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46512236 | ACTCCTTCTTCGGTC[A/G]TCTCTTCCTTTGGGC | 55626 |
rs59967271 | in-del | -/ATAGATAGATAGATAG | 0 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46447764 | TAGATAGATAGATAG[-/ATAGATAGATAGATAG]TGATGGCAAATACTA | 55626 |
rs60234540 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46586039 | GAACTCCCAACCTCA[A/G]GTGATCCACCCGCCT | 55626 |
rs60401088 | snp | C/T | 0.145978 | 0.227331 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46518666 | AGATGTTCGCCCATT[C/T]CTGCTCTAAAACATT | 55626 |
rs60418060 | in-del | -/AAAA | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46445384 | TGTGCTGTCAGTGAG[-/AAAA]TCCACTGACCTCAAA | 55626 |
rs60423999 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46511610 | CCCCACAACTGTAAA[C/T]TACCCTTTTCTTTTG | 55626 |
rs60534052 | snp | C/T | 0.0337553 | 0.125452 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46585194 | CCCTAATCTCAAGTA[C/T]CCAGGGACACAAACA | 55626 |
rs60573183 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46468366 | GCAATATAGTGAGAC[C/T]TCATCTCTTGAAAAA | 55626 |
rs60592464 | in-del | -/A | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46569441 | ATTAAAAAAAAAAAA[-/A]TATATATATATATAT | 55626 |
rs60890473 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46438538 | GCATTAGATACCGAT[C/T]TGGAAAACCCAAGGG | 55626 |
rs60898911 | in-del | -/A | 0 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46466359 | CTAAAAAAAAAAAAA[-/A]GGGCAATGTGAGTAT | 55626 |
rs60987620 | in-del | -/A | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46563862 | AAAAAAAAAAAAAAA[-/A]GGCCAGGCGTGGTGG | 55626 |
rs61137173 | in-del | -/TAAATATGTATTTTATTATTTATATA | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46418325 | TTTATTATTTATATA[-/TAAATATGTATTTTATTATTTATATA]AATATATATTTTATT | 55626 |
rs61241780 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46473674 | TGTTTGTTTTTGAGA[C/T]GGAGTCTCGCACTGT | 55626 |
rs61397837 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46557123 | CCTGGGCAACAAGAG[C/G/T]GAAACTCCATCTCAA | 55626 |
rs61437409 | in-del | -/ACAC/ACACACACACA/ACACACACACACACACACACACACACAC | 0.5 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46420021 | CACACACACACACAC[lengthTooLong]TCTTCCAGGTGTTGT | 55626 |
rs61451984 | snp | A/C | 0.0298908 | 0.118541 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46436811 | GCTCAGAAAAATAAA[A/C]AGAAACTAACAATTT | 55626 |
rs61487456 | in-del | -/ATCA | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46543487 | AACTAACCACTGACA[-/ATCA]TCCAAGGAAAACAAT | 55626 |
rs61588181 | in-del | -/A | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46588624 | TACTAAAAAAAAAAA[-/A]GTACAAAAATTAGCC | 55626 |
rs61733783 | snp | A/T | 0.0253123 | 0.109615 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46397576 | GCTGGGAAGGGAAAC[A/T]GGAATGGGGACAGGG | 55626 |
rs61882690 | snp | G/T | 0.0142736 | 0.0832652 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46400026 | GCACAGCCCAGGCAC[G/T]TGGTCAACGGTGCCT | 55626 |
rs61882691 | snp | A/C | 0.196771 | 0.244268 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46417165 | CAAGCGATTCCCCTG[A/C]CTCAGCCTCCTGAGT | 55626 |
rs61882701 | snp | A/G | 0.282632 | 0.247861 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46421725 | ATTAGCCCTACAGAT[A/G]AGAGACTATCTGGAC | 55626 |
rs61882702 | snp | A/G | 0.204189 | 0.245767 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46429271 | CGCTACTCAGAAATC[A/G]GTGTGTGGGGAGTGG | 55626 |
rs61882703 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46433705 | TTCACTCTTACTCTT[A/G]TCTTTTTCTCTAATC | 55626 |
rs61882704 | snp | C/T | 0.0670745 | 0.170406 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46433983 | AGTCAGGCGTGGTTG[C/T]GCATGCCTGTAATAC | 55626 |
rs61882705 | snp | A/T | 0.5 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46439558 | TCAAAGACTTAACTA[A/T]TAAAAAACTAAAATA | 55626 |
rs61882706 | snp | A/G | 0.202035 | 0.245356 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46441236 | AAGATAAGCTGGGCC[A/G]GGCACGGTGGCTCAC | 55626 |
rs61882708 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46449489 | GTACAAGGTCTATAG[A/G]AGGAAAGCTACAAAA | 55626 |
rs61882709 | snp | A/G | 0.312104 | 0.242163 | intron-variant, upstream-variant-2KB | AMBRA1, MIR3160-2 | GRCh38.p7 | 11:46450864 | AACCCTAATGTAAAC[A/G]CATACTTTGAGTGAT | 55626 |
rs61882710 | snp | A/G | 0.20111 | 0.245173 | intron-variant, upstream-variant-2KB | AMBRA1, MIR3160-1 | GRCh38.p7 | 11:46452392 | CTCACTATGTTGCCC[A/G]GCTTGCCTTGAACTC | 55626 |
rs61882711 | snp | C/T | 0.202343 | 0.245416 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46457930 | AAAAAAAAGACATTC[C/T]ACCCTACTGGCCCAG | 55626 |
rs61882712 | snp | C/T | 0.197082 | 0.244335 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46462398 | ATCTATCTTCCTCTT[C/T]ACTCTCCTCACGTCT | 55626 |
rs61882713 | snp | G/T | 0.5 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46467569 | TTTTTTTTTTTTTGG[G/T]ATGGAGTCTCACTCT | 55626 |
rs61882715 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46510248 | CAAGAGCTAGTTCCT[A/G]AAAGCCTCAACTGGA | 55626 |
rs61882716 | snp | A/T | 0.0154538 | 0.0865337 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46510257 | GTTCCTAAAAGCCTC[A/T]ACTGGAGGAACTTTC | 55626 |
rs61882717 | snp | C/T | 0.5 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46512909 | ATATATAACTTTCCC[C/T]TTTTGCAGCCAGCTA | 55626 |
rs61882718 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46512913 | ATAACTTTCCCCTTT[C/T]GCAGCCAGCTAACGC | 55626 |
rs61882719 | snp | A/G | 0.489608 | 0.0713316 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46517392 | GACCTCAGGTGATCC[A/G]CCCGCCTCGGCCTCC | 55626 |
rs61882720 | snp | A/C | 0.202959 | 0.245534 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46517438 | ACAGGCGTAAGCCAC[A/C]GCGCCCGGCTAGAAA | 55626 |
rs61882721 | snp | G/T | 0.0154538 | 0.0865337 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46518738 | AAAAGAACTTGAAAT[G/T]AAAGTATTGTGCACT | 55626 |
rs61882722 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46519670 | ACCGCTATTTCCATC[C/T]GGGAGCACCAAACCC | 55626 |
rs61882723 | snp | A/G | 0.5 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46524693 | ACAGTCTAATAAACA[A/G]CCATTACTATTTTTT | 55626 |
rs61882743 | snp | C/G | 0.438666 | 0.164028 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46527204 | GAAGTAGGAGGCCAG[C/G]AGCAGTTGCTCACTC | 55626 |
rs61882744 | snp | G/T | 0.0441842 | 0.1423 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46528675 | CAGAGTTTCAGTCAC[G/T]CAAGATGAAGAGGTT | 55626 |
rs61882745 | snp | A/C | 0.5 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46543697 | GGAAGCAAAATGTCA[A/C]CCAGCCAGAGGCACA | 55626 |
rs61882746 | snp | C/T | 0.323197 | 0.239044 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46545925 | GATGTAGAAGATCAG[C/T]GATCTGGTAGTGCCA | 55626 |
rs61882748 | snp | C/G | 0.313326 | 0.241847 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46557051 | TGAGGCAGGAGAATC[C/G]CTTGAACCCGGGAGG | 55626 |
rs61882749 | snp | A/C | 0 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46558576 | AAAAAAAAAAAAAAC[A/C]ACTACCTACCTAGTA | 55626 |
rs61882750 | snp | G/T | 0.323197 | 0.239044 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46562677 | AGCAGATTAAAGGGA[G/T]AAATCAATAGTTTAG | 55626 |
rs61882751 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46583717 | AGTGGGCGAAGGACA[A/T]GAACAGACACTTCTG | 55626 |
rs61882752 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46583779 | ATGAAAAAATGCTCA[C/T]CATCACTGGCCATCA | 55626 |
rs61882753 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46583816 | TGCAAATCAAAACCA[C/T]AATGAGATACCATCT | 55626 |
rs61882754 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46586051 | TCAGGTGATCCACCC[A/G]CCTCAGCCTCCCAAA | 55626 |
rs61882755 | snp | C/T | 0.0429648 | 0.14013 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46588170 | AAACCTGGTCTCTAC[C/T]AAAAATACAAAATTA | 55626 |
rs61882756 | snp | C/T | 0.202651 | 0.245475 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46588733 | TGAGCCGAGATCGCG[C/T]CATTGCACACCAGAT | 55626 |
rs61882757 | snp | A/G | 0.272511 | 0.248984 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46589689 | CAGTGGTGCTAACTC[A/G]GCTAACTGCAAGCTC | 55626 |
rs61882758 | snp | A/G | 0.323434 | 0.238972 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46590255 | GCGCACCTGTAGTCC[A/G]CTTGAACCCAGGAGG | 55626 |
rs61882759 | snp | A/C | | | intron-variant, upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46593101 | AAAAGCAAAACAGCC[A/C]AGAAACCACATGGTT | 55626 |
rs61999319 | snp | A/G | 0.0320498 | 0.122465 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46434894 | GGTTATGGGGGGCCA[A/G]GGAGTACACTGCCAG | 55626 |
rs68002803 | snp | C/T | 0.499946 | 0.00519141 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46517560 | ACTAAACAGGCCGGG[C/T]GCAGTGGCTCACGCC | 55626 |
rs71038902 | in-del | -/A/AAAA | 0 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46428602 | TAGCCAAAAAACCTT[-/A/AAAA]AAAAAAAAAAGAAGA | 55626 |
rs71042606 | in-del | -/A | 0 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46513282 | GTACTCAATTCTCAC[-/A]AAAAAAAAAAAAAAG | 55626 |
rs71042607 | in-del | -/T | 0 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46578908 | CTCAAAGCTCTATAC[-/T]TTTTTTTTTTTTTTT | 55626 |
rs71451648 | in-del | -/A | 0.5 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46405505 | GGGAGGCTTGCTTGA[-/A]GCTAGGAGTTCAAGA | 55626 |
rs71451651 | in-del | -/C | 0.5 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46459705 | ACAGAGCAAGACTCC[-/C]ATCTCCCTCCCAAAA | 55626 |
rs71451652 | in-del | -/G | 0.5 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46489433 | CAGGCGTGAGCCACC[-/G]GCACCTGGCCAGTTT | 55626 |
rs71451653 | in-del | -/A | 0.5 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46507176 | GCAAGACTCCGTCTC[-/A]AAAAAAAAAAAAAAA | 55626 |
rs71451654 | in-del | -/T | 0.5 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46513268 | CTACGCTCTTTTTTC[-/T]TTTTTTTTTTTTTTG | 55626 |
rs71451655 | in-del | -/G | 0.5 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46515335 | AAAGTAGCCAGGCGT[-/G]GGTGGTGCGTGCCTA | 55626 |
rs71455291 | in-del | -/C | 0.5 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46519290 | TGGCCTCCCAACATG[-/C]TGGGATTACAGGCAT | 55626 |
rs71455292 | in-del | -/C | 0.5 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46530923 | ATTCTCGCTCTGTAG[-/C]CCCAGGCTGGAGTGC | 55626 |
rs71455293 | multinucleotide-polymorphism | CG/TA | 0.5 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46553131 | TATTTTTAGTAGAGA[CG/TA]GGGTTTCACCATGTT | 55626 |
rs71474178 | snp | A/G | 0.5 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46431546 | CTGTGCTAAGATGGA[A/G]AACTGGCAGGCTGTG | 55626 |
rs71474179 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46505750 | AGGAAAATCGAGGGG[A/G]AAGGAAGGGGAGAGA | 55626 |
rs71474180 | snp | C/T | 0.5 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46517101 | GAAATATTACAACTT[C/T]TGCTATATAATATAT | 55626 |
rs71474181 | snp | A/G | 0.5 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46518454 | AAAAAAAAAAAAAAA[A/G]GAATTACTCACTTTG | 55626 |
rs71474182 | snp | C/T | 0.5 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46539497 | AGGAGATGGAGGTTG[C/T]GGTGAGCCGAGATCA | 55626 |
rs71474183 | snp | C/G/T | 0.5 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46563831 | AGTCTGGCAACAAAG[C/G/T]GAGACTGTCTCAAAA | 55626 |
rs71474184 | snp | A/C | 0.02016 | 0.0983543 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46564154 | CGTCTCAAAAAAAAA[A/C]AAAAAAAAAACGTAA | 55626 |
rs71474185 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46569886 | GAATCACTTGAACCC[A/G]GAAGGCGGAGGTTGC | 55626 |
rs71481425 | multinucleotide-polymorphism | ATTAGCCGGGTGTGGTGGCAGGCGCCTGTAG/GTTAGCTAGGCGTGATGGTACGCGCCTGTAA | 0.5 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46553080 | ACTAAAAATACAAAA[lengthTooLong]TCCCAGCTACTCGGG | 55626 |
rs72022141 | in-del | -/TAGATAGATAGA | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46447709 | AGCCAGACCATCTTG[-/TAGATAGATAGA]TAGATAGATAGATAG | 55626 |
rs72438253 | in-del | -/CTTT | 0.112983 | 0.209108 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46413478 | TACTGAAACTCTTAG[-/CTTT]CTTTCTTTCTTTCTC | 55626 |
rs72910096 | snp | A/G | 0.0103295 | 0.0711199 | downstream-variant-500B | AMBRA1 | GRCh38.p7 | 11:46396101 | TGTAGTCCTGGGTGG[A/G]AAGCTATTAGGATGA | 55626 |
rs72910097 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46398073 | AAGACTCGCTCCATC[A/T]CTGTGAAAACCAATC | 55626 |
rs72910100 | snp | A/C/G/T | 0.0349297 | 0.127459 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46408531 | CACCAGGACCTGAGG[A/C/G/T]GGCTGTCCCTGGCTC | 55626 |
rs72910102 | snp | G/T | 0.0792508 | 0.182605 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46424246 | GGCAAACAGCAAACA[G/T]CCTTTTTTTTTTTTT | 55626 |
rs72912114 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46474272 | AATATTAGAACCACC[A/G]GAGGAAAATACTTTC | 55626 |
rs72912116 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46475651 | GCCATTCCCAGTTTG[A/G]TAATTTGTTTCAGTT | 55626 |
rs72912118 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46484384 | TATACTGAGTCATTA[C/T]AGATTAGAGAGAATC | 55626 |
rs72912125 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46519420 | GACAACTCCTCCTTA[C/T]TAAAAAATTATAACC | 55626 |
rs72912131 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46528552 | GACAAATACTGCAAG[A/G]TTCCATTAATAAGAG | 55626 |
rs72912134 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46529934 | ATCCTGGGCCCACCC[C/T]CCAACCACTCAATAA | 55626 |
rs72912137 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46534614 | CAAGCCCAACTCTCA[A/G]CGTTATTAGGAAGAA | 55626 |
rs72912138 | snp | A/T | 0.0349115 | 0.127424 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46552909 | TTCACTTTTTAATTT[A/T]AAAAATTATTATTAC | 55626 |
rs72912144 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46574735 | CCAACTCTTGGGCAC[C/T]TCCAAAGAATACTTT | 55626 |
rs73449906 | snp | A/G | 0.0298908 | 0.118541 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46524830 | TGAAGAAGGGTGAAT[A/G]CTATAAAGGTATAAA | 55626 |
rs73449908 | snp | C/T | 0.030278 | 0.119257 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46526201 | ACAAGAGCGAAACAT[C/T]GGCTCAAAAATAAAT | 55626 |
rs73449917 | snp | A/G | 0.0314385 | 0.121371 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46534215 | CACCTGGTGCCAGCC[A/G]GGTGCGGTGGCTCAG | 55626 |
rs73449920 | snp | A/G | 0.0298908 | 0.118541 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46537256 | TGACCTACATGAGCA[A/G]CAGAGGTTTTGACAA | 55626 |
rs73449929 | snp | A/G | 1.67829e-05 | 0.00289675 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46543262 | CCCACCTGGATGCCA[A/G]AAGAGCGGGAGGACA | 55626 |
rs73449937 | snp | C/T | 0.030278 | 0.119257 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46549716 | TCAAAACTCAAGCAA[C/T]GACTTTGGACGTTTA | 55626 |
rs73449939 | snp | C/T | 0.030278 | 0.119257 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46555302 | ATTAGAAGTTAGATT[C/T]AGAGGTTCCTTGTGC | 55626 |
rs73449943 | snp | A/T | 0.0298908 | 0.118541 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46558065 | CCTTCTTAGACCTTC[A/T]AACCTAGCCCAACCA | 55626 |
rs73449949 | snp | C/G | 0.0298908 | 0.118541 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46560980 | TTTCAAATCATAAAG[C/G]ATCACATCTTTCTAT | 55626 |
rs73449951 | snp | C/T | 0.0298908 | 0.118541 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46561590 | TTCCTTCAGATAGTA[C/T]CAGAGCTACACTCCC | 55626 |
rs73449956 | snp | A/G | 0.0298908 | 0.118541 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46564402 | CCTCACAATGATACT[A/G]TGAAGATGGGTACTG | 55626 |
rs73449974 | snp | A/C | 0.0298908 | 0.118541 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46578965 | ATAGAAATAAGAGCC[A/C]ATAAACAAGTGAATG | 55626 |
rs73449978 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46587100 | AAACACAACTTCAGG[G/T]CAGGCACAGTGGCTC | 55626 |
rs73449983 | snp | A/G | 0.314301 | 0.241589 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46590782 | CGGGCATGGTGGCAC[A/G]CGCCTGTAATCCCAG | 55626 |
rs73466034 | snp | C/T | 0.131038 | 0.219882 | utr-variant-3-prime, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46397321 | GATCTTCCTCTCCAC[C/T]CTGACCCTCTTCCTC | 55626 |
rs73466036 | snp | A/C | 0.131038 | 0.219882 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46399809 | CCGGAAAAGAGTCAA[A/C]TGACCAGCACAGGAC | 55626 |
rs73466042 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46404813 | CCTCTGTCCCCATCC[C/T]CCCAAAAGAATGAAA | 55626 |
rs73466069 | snp | A/C | 0.0314385 | 0.121371 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46441060 | TTGCTAACAATCTGA[A/C]AGAAGACAGAAAAGC | 55626 |
rs73466072 | snp | A/G | 0.5 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46443199 | AAAAGAAGAGAAAGA[A/G]AAGGGAGTGTAGGAT | 55626 |
rs73466080 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46447932 | AATAGTGATGGCAAA[C/T]ACTAAGTGTCTAATA | 55626 |
rs73466088 | snp | C/T | 0.0314385 | 0.121371 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46465484 | TAAGTTTTTACCATA[C/T]TTTCTCAGAGAGTTC | 55626 |
rs73466094 | snp | C/T | 0.0298908 | 0.118541 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46466379 | AATGTGAGTATCTAA[C/T]GAGGAGACCAACCAC | 55626 |
rs73466095 | snp | A/G | 0.031825 | 0.122064 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46471960 | AGGATTTGTTGCCTC[A/G]TTTCACATCCACATT | 55626 |
rs73466099 | snp | C/T | 0.0314385 | 0.121371 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46477735 | AGAGCCCCCAGCCCA[C/T]CAGCGACTGAGGTGG | 55626 |
rs73467915 | snp | A/C | 0.136847 | 0.222927 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46488466 | CAAAACAAAACAAAA[A/C]AAAAAACTGACAAAA | 55626 |
rs73467917 | snp | C/T | 0.0298908 | 0.118541 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46488613 | CCAAGTAGATTTAAC[C/T]GACATCTACAGGACA | 55626 |
rs73467919 | snp | C/T | 0.0298908 | 0.118541 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46493854 | CCAAGATTGGTCCTT[C/T]CGCAGATTTGTATCT | 55626 |
rs73467920 | snp | A/G/T | 0.0298908 | 0.118541 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46499351 | AAGCACAATCCAGAC[A/G/T]TGTTCCATTTTCTTT | 55626 |
rs73467929 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46503138 | TATAGCAGAAGAGGA[C/T]TAGCTTCTGGCCTAT | 55626 |
rs73467936 | snp | C/G | 0.0298908 | 0.118541 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46506598 | CCCCAGACCTGACCC[C/G]GCTATGTCAAGATGG | 55626 |
rs73467938 | snp | C/T | 0.0298908 | 0.118541 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46506872 | AACCCAGCAATAAGA[C/T]TGGCTAGCTTAGGCT | 55626 |
rs73467941 | snp | A/G | 0.030278 | 0.119257 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46506892 | TAGCTTAGGCTGGGC[A/G]TGGTTGCTCACACCT | 55626 |
rs73467944 | snp | C/T | 0.0298908 | 0.118541 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46509212 | ACATTCTTCAAACTA[C/T]GGCTTTAATATCTTG | 55626 |
rs73467946 | snp | C/T | 0.0410537 | 0.137264 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46511338 | TGCCTGTTTTAAAGT[C/T]ATCAATCCTTATGTT | 55626 |
rs73467947 | snp | C/T | 0.0352966 | 0.128072 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46514411 | CCCATACTTAGACAC[C/T]TGTAACAATCCTACC | 55626 |
rs73467950 | snp | A/G | 0.0298908 | 0.118541 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46516141 | GTGCCTACTTACTAC[A/G]GAATGTGTTGGCAAC | 55626 |
rs73467963 | snp | C/G | 0.0314385 | 0.121371 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46519825 | TTTACAAACTTTTTG[C/G]TCCCAGGACTCCTTT | 55626 |
rs73467964 | snp | A/G | 0.0298908 | 0.118541 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46522939 | GTAAAATCTTAGGAC[A/G]AATATCAGAAAGGCA | 55626 |
rs73467966 | snp | A/G | 0.0298908 | 0.118541 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46524260 | AGTGGAATGCCCCCC[A/G]GAAATGTGGCAATGT | 55626 |
rs74236421 | snp | C/T | 0.0111196 | 0.0737302 | downstream-variant-500B | AMBRA1 | GRCh38.p7 | 11:46396319 | CACCAGAAACAGTGC[C/T]GGGAGAACCTGGGCC | 55626 |
rs74324759 | snp | A/T | 0.5 | 0 | upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46595062 | GACTCCAGTCTCTAT[A/T]AAAAAAAAATAAATA | 55626 |
rs74337824 | snp | A/C | 0.5 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46517833 | CAGACTCTGTCTCAA[A/C]AAAAAAAAAAAAAAA | 55626 |
rs74362589 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46465438 | ACGTTACTACAGTTA[C/T]GTGTAGGTGTTTTTT | 55626 |
rs74374232 | snp | A/G | 0.5 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46533167 | GACTCTGTCTCAAAA[A/G]AAAAAAAAAAAAGGA | 55626 |
rs74419278 | in-del | -/TAG | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46401259 | TCTCAGCTCTTTTCG[-/TAG]AGACAGAGTCTCGCT | 55626 |
rs74493944 | snp | A/C | 0.5 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46557300 | AGTGAGACTCCATCT[A/C]AAAAAAAAAAAAAAA | 55626 |
rs74553660 | snp | C/T | 0.0150606 | 0.0854603 | upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46594132 | AAACAGCTCAACTCC[C/T]ACTCAAGGTCCGGCT | 55626 |
rs74563206 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46585360 | AATAAAAATAAATAA[A/T]TAAATAAATAATTCC | 55626 |
rs74587022 | snp | A/C | 0.5 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46527799 | AAAAAGAAAAAAAAA[A/C]CAGGAAATAACAAGT | 55626 |
rs74648942 | snp | A/C/G | 0.00914647 | 0.0670416 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46550240 | ACCTTTATTTCCTGT[A/C/G]AACAGCAGGTTAGGT | 55626 |
rs74650395 | snp | A/G | 0.0150606 | 0.0854603 | upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46594578 | CCTTAAGGCAGGGGG[A/G]AAAAAAGCACACGGA | 55626 |
rs74687384 | snp | A/G | 0 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46567491 | CTGCCTCAGCCTTCC[A/G]AGTAGCTGGGAGTAC | 55626 |
rs74717050 | snp | A/T | 0 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46525763 | CTCAAAAAAAAAAAA[A/T]TTAGCCAGCATGGTG | 55626 |
rs74775768 | snp | A/G | 0.112631 | 0.208878 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46539752 | GACTTGCATAGAGTC[A/G]TTGTTGAAGGCAGAA | 55626 |
rs74816158 | snp | A/G | 0.0898077 | 0.191933 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46432186 | GGAGAAGAGAGTGAC[A/G]TGGAAACAAATAACT | 55626 |
rs74821485 | snp | C/G | 0.111224 | 0.207945 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46472592 | AGTCAGGAGAACAAC[C/G]TGTCAACTTCTAGTT | 55626 |
rs74866322 | snp | C/T | 0.089084 | 0.191327 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46398435 | GCTGTCTTCCTTCAG[C/T]GTAGTTTTGTGTTAC | 55626 |
rs74910564 | in-del | -/AA | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46488471 | CAAAACAAAAAAAAA[-/AA]CTGACAAAATTGAAG | 55626 |
rs74912487 | snp | C/T | 0.0418186 | 0.138422 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46579617 | GGCAAGATACCAAGC[C/T]AAGCAGCCAAGAATA | 55626 |
rs74933558 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46513093 | ATCTTCTTTCTATTT[A/G]CAGTACCTCCAGTAG | 55626 |
rs74973609 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46562121 | GTGAAAGAAAACAAC[A/G]CACCCTTTTACCTGG | 55626 |
rs74974187 | snp | C/G | 0.0298908 | 0.118541 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46472388 | GCAAATAACCTGGGT[C/G]CTAGGACATATATTT | 55626 |
rs75140599 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46585354 | ATGATCAATAAAAAT[A/T]AATAAATAAATAAAT | 55626 |
rs75217035 | snp | A/C | 0.104504 | 0.2033 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46533284 | ATCTCTGAGCAGTGG[A/C]TTTAAGAGGATATCC | 55626 |
rs75307275 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46551601 | CGACACCAGGCGCGA[C/T]GGCTCACGCCTGTAA | 55626 |
rs75318032 | snp | A/C | 0.5 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46536891 | CAGTCTTCATCTATC[A/C]TGAGAGAAAAAGACC | 55626 |
rs75331995 | snp | A/G | 0.0298908 | 0.118541 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46437171 | GGAGAGTACAAGTAA[A/G]ATTTTCCTTCTTCTG | 55626 |
rs75349647 | in-del | -/G | 0.0829062 | 0.185956 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46456477 | AATGCAGCTGCTTAA[-/G]GGGGTGCCTCAGCAG | 55626 |
rs75385039 | snp | A/C | 0.5 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46582110 | ACAGAGACCCTGTCT[A/C]AAAAAAAAAAAAAAA | 55626 |
rs75480787 | snp | A/G | 0.0916144 | 0.193427 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46490521 | GGGAGGAAGTAGAAC[A/G]GATCTTGATTTTCCG | 55626 |
rs75481159 | snp | A/C | 0 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46588777 | CGAAACTCCATCTCA[A/C]AAAAAAAAAAAAAAA | 55626 |
rs75486765 | snp | C/G | 0.0389884 | 0.134067 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46543945 | AGAACTCACAGTTTA[C/G]CTGGAATTGGAACTG | 55626 |
rs75494138 | snp | C/T | 0.0596104 | 0.162024 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46443811 | TGTGGAAATATAATC[C/T]CATTCATCAGTCCTT | 55626 |
rs75516281 | snp | A/C | 0.5 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46527800 | AAAAGAAAAAAAAAA[A/C]AGGAAATAACAAGTG | 55626 |
rs75625771 | snp | A/G | 0 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46520143 | AAACTCCGCCTCGAA[A/G]AAAAAAAAAAAAAAA | 55626 |
rs75656553 | snp | A/C | 0.5 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46434115 | AGTGAAACTCCGTCT[A/C]AAAAAAAAAAAAAAA | 55626 |
rs75680994 | snp | A/C | 0.0916144 | 0.193427 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46590540 | ACGATATACAAAACT[A/C]ATCTTTTTCAAGTGA | 55626 |
rs75704361 | snp | C/G | 0.5 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46537875 | TTTCAAGTACAATCA[C/G]CTTTTATGAACTCCA | 55626 |
rs75707167 | snp | C/T | 0.5 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46454344 | AACTGTGAAATATTC[C/T]TATGTATCACAGCTT | 55626 |
rs75721114 | snp | A/G | 0.5 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46590468 | GACCTCATCTCTTCA[A/G]GAAAAAAAAAAAATT | 55626 |
rs75743621 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46563153 | ATCACACCTGTAACC[C/T]AGCTAACTCAGGAGG | 55626 |
rs75748389 | snp | C/G | 0.271972 | 0.249033 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46435709 | CAATGTCCATGACAG[C/G]CCTAGTCTGCACTTT | 55626 |
rs75762469 | snp | A/G | 0.0916144 | 0.193427 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46497541 | GAGAGGACCCAGCAC[A/G]ACCAGGAAAATGTGA | 55626 |
rs75833560 | snp | C/T | 0.0391387 | 0.134304 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46522325 | TGTAAGACTTGAATG[C/T]ATAATAAAAACTCAC | 55626 |
rs76008953 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46562107 | AGAAAATATGGCAGG[G/T]GAAAGAAAACAACAC | 55626 |
rs76018124 | snp | C/T | 0.0930568 | 0.194599 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46461409 | AAATTTCTGGGCATA[C/T]GTTTGCAAGTATTTT | 55626 |
rs76034988 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46557959 | CCTGGGCGACTGAGC[A/G]AGACTCAGAGAGGAC | 55626 |
rs76039883 | snp | C/T | 0.0418186 | 0.138422 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46500521 | ATCAGAGTTAGCTGC[C/T]TAAAATATATATTGG | 55626 |
rs76119949 | snp | C/G | 0.0154538 | 0.0865337 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46558170 | AAATTCCTAACCTGA[C/G]TAATTATGAGACAAA | 55626 |
rs76149764 | snp | C/T | 0.0387552 | 0.1337 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46448198 | GCCAAGACAGACCAC[C/T]TTCTGGGCCACAAAA | 55626 |
rs76191706 | snp | A/C/T | 0.00953873 | 0.0683987 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46525765 | CAAAAAAAAAAAAAT[A/C/T]AGCCAGCATGGTGGC | 55626 |
rs76266079 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46444740 | TTTCTTTTAGAGAGC[A/G]GCATTTATTGCACTG | 55626 |
rs76269141 | snp | A/C | 0.5 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46557303 | GAGACTCCATCTCAA[A/C]AAAAAAAAAAAAAAG | 55626 |
rs76335951 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46427262 | CTATAGTTACCACTA[A/G]TTTGAGAAGTCTGGA | 55626 |
rs76419346 | snp | A/C | | | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46548374 | TCTTTTCTGGGACAA[A/C]CTTCATGGCGCTCAG | 55626 |
rs76486823 | snp | A/C/G | 1.654e-05 | 0.00287571 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46547152 | CCCATCTAGGCAGCC[A/C/G]GAAGCAATAAGGCCT | 55626 |
rs76496500 | snp | A/G | 0.5 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46500294 | TAGCATTTTTTTTTT[A/G]GACAAGAAAAGTAAG | 55626 |
rs76553194 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46576584 | CTTCATAATATCCCT[C/T]GGTAACAACATTTCA | 55626 |
rs76564523 | snp | A/C | 0.5 | 0 | intron-variant, upstream-variant-2KB | AMBRA1, MIR3160-2 | GRCh38.p7 | 11:46450056 | AGAGCGAGACTGTCT[A/C]AAAAAAAAAAAAAAA | 55626 |
rs76641616 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46402353 | CTGCCCATTGTGGGA[A/G]AAGCATTTATTTTAT | 55626 |
rs76650979 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46444333 | GGTTTAACTTTCTCT[A/G]AGATATATTCTTCTG | 55626 |
rs76713300 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46513542 | AGGTATGACTACATA[C/T]ATGAGAACACTGGGC | 55626 |
rs76745806 | snp | A/G | 0.5 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46430238 | CAGACAGCCAAAAAA[A/G]CTGAGTTTGGTAGGA | 55626 |
rs76746241 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46477500 | TCAGCTAATTTCTGG[A/G]AAAAAAAAAAAAAAA | 55626 |
rs76752406 | snp | C/G/T | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46424536 | ATACTGAGGCACTCA[C/G/T]GGCTTCTGGAATTCC | 55626 |
rs76755912 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46576838 | GATTAAGAGTCTTAA[A/G]TTCCTAATTCCATCA | 55626 |
rs76758799 | snp | A/G | 0.0387552 | 0.1337 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46530850 | TTTATCTCCATAAAT[A/G]GTTTTTTTGGAACAC | 55626 |
rs76776926 | snp | A/T | 0 | 0 | intron-variant, upstream-variant-2KB | AMBRA1, MIR3160-2 | GRCh38.p7 | 11:46450436 | CAGGTGAGCACAAGA[A/T]TTTTTTTTTTTTTCT | 55626 |
rs76886784 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46570662 | TGATTGCTGTTAATA[A/C/T]TTTTTTTTAAGCCAG | 55626 |
rs77004997 | snp | A/C/G | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46561056 | ACCACATTGCCCCCA[A/C/G]TTCTTCCTGGAAACC | 55626 |
rs77040995 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46521620 | ATTATGATTTCCAAA[C/T]TGACATCTCTGCTCT | 55626 |
rs77047001 | snp | A/G | 0.5 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46507497 | AAAAAAAAAAAAAAA[A/G]ATTGGCTAGCTTAAA | 55626 |
rs77068727 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46580734 | TAACCATACTTCCCC[A/G]ATTTCTTCTCTTTCC | 55626 |
rs77161239 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46432878 | CGTTCACTCAGGCAC[A/G]TTAGTCTGGCTGAGG | 55626 |
rs77180536 | snp | A/C | 0 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46548994 | CAAGACTCCATCTCA[A/C]AAAAAAAAAGATTAT | 55626 |
rs77191199 | snp | C/T | 0.0418186 | 0.138422 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46445832 | TCAGTACATGATGAA[C/T]AAAATGCTAGTTGCT | 55626 |
rs77222873 | snp | C/T | 0.5 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46459739 | AAAAAAAAATACACA[C/T]ACACACACACACACA | 55626 |
rs77240132 | snp | G/T | 0.5 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46403805 | ATGAGAAGTAGCCTA[G/T]GAGCCCTTTGGTGCT | 55626 |
rs77244134 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46590061 | CACATATTGAAAATA[C/T]TGTGAAAATTATACA | 55626 |
rs77255340 | in-del | -/TAGATCTC | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46419407 | ACAAAACAATATCTC[-/TAGATCTC]AACTTAGAACAAACA | 55626 |
rs77271839 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46455571 | ATATAACCTCTTGAT[C/T]TGTCATGGCCAGAAT | 55626 |
rs77311007 | snp | G/T | 0.5 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46520614 | TTTTTTTTTTTTTTT[G/T]AGACGGAGTCTCGCT | 55626 |
rs77312978 | snp | G/T | 0.5 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46467566 | TTTTTTTTTTTTTTT[G/T]GGGATGGAGTCTCAC | 55626 |
rs77360195 | snp | A/G | 0.5 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46478026 | GTTTACTGGTGAATG[A/G]AAAAAAAAAAGAATG | 55626 |
rs77438943 | snp | G/T | 0.5 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46454892 | TTTTTTTTTTTTTTT[G/T]AGATGGAGATGGGTT | 55626 |
rs77450193 | snp | C/G | 0.00260005 | 0.035962 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542715 | TCTGGGCGGGGGCAT[C/G]GATTCCGCCTCAGAG | 55626 |
rs77457592 | snp | C/T | | | intron-variant, downstream-variant-500B, upstream-variant-2KB | AMBRA1, MIR3160-1, MIR3160-2 | GRCh38.p7 | 11:46451484 | AAAACAGCTTCACAG[C/T]TTCTCTCTAAGATTT | 55626 |
rs77473419 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46573102 | GCAAAACTCTGTCTC[A/C]AAAAAAAAAAAAAGG | 55626 |
rs77515479 | snp | A/T | 0.5 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46500284 | AAAAAGGACTTAGCA[A/T]TTTTTTTTTAGACAA | 55626 |
rs77536620 | snp | A/C | 0.5 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46400300 | CCAGCAGCTATTTTT[A/C]TGAGACTTTCTTTGC | 55626 |
rs77561648 | snp | C/T | 0.0387552 | 0.1337 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46462174 | TCTCCCAGAAAACCC[C/T]GGACCTGCTATCACA | 55626 |
rs77604651 | snp | C/T | 0.5 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46477323 | TTTAAAGATACTTCT[C/T]TTTTTTTTTTTTGAG | 55626 |
rs77680372 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46418787 | TGGCTCTAATAATGC[A/G]CTCTCCTTAGAGCCT | 55626 |
rs77689289 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46398097 | ACCAATCCGAGTCTT[A/G]AAAGCTAGACAAAAC | 55626 |
rs77752201 | snp | A/T | 0.5 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46439560 | AAAGACTTAACTATT[A/T]AAAAACTAAAATATA | 55626 |
rs77763301 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46582181 | ATCCTCATTCTATGC[C/T]TCTTTCCTCCATCCC | 55626 |
rs77774199 | snp | A/G | 0.0726307 | 0.176182 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46505454 | ACTACTAATGTTGAG[A/G]TGACTAATCCACAGC | 55626 |
rs77814874 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46455038 | GTGTACGCCACCCCA[C/T]ACCCAGCTAATTAAA | 55626 |
rs77817298 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46506102 | ACCGTATCTACAGGA[A/G]AACATATTTCACTGT | 55626 |
rs77887980 | snp | A/G | 0.5 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46425308 | TCTTTTGCTTGATCC[A/G]TTTGTGTGTGTGTGT | 55626 |
rs77895324 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46535202 | TGCCGAACTTCTAAC[C/T]AAGAAGAACTCAGAA | 55626 |
rs77916020 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46495447 | TAAATGACAAATCAA[C/T]ACCAGGGATATTGGA | 55626 |
rs77940349 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46566872 | CGCCATTGTAAAACT[A/G]ATAAAAGGCCCCAAG | 55626 |
rs78009650 | in-del | -/GTT | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46533258 | ACACACACACAAATT[-/GTT]AATAGCAGATCTCTG | 55626 |
rs78022549 | snp | C/T | 0.0387552 | 0.1337 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46495600 | AGAGATAAGACTATA[C/T]GGAATGTAAAAGGGG | 55626 |
rs78063664 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46432299 | AGATGGATGCCACAG[A/G]AAGTAAAAAGCTTGC | 55626 |
rs78099039 | snp | A/T | 0 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46557151 | CAAAAAAAAAAAAAA[A/T]TTAGCCAGGCATGGT | 55626 |
rs78132848 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46423025 | AATGATGGGAATTAA[A/G]GAAGGCTTAAGGTTT | 55626 |
rs78171794 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant, upstream-variant-2KB | AMBRA1, MIR3160-2 | GRCh38.p7 | 11:46450270 | CAAAAAGACATGGAG[A/G]AACCTTAAGTGCATG | 55626 |
rs78185204 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46430237 | GCAGACAGCCAAAAA[A/G]GCTGAGTTTGGTAGG | 55626 |
rs78185731 | snp | G/T | 0.5 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46460338 | TCTTTTTTTTTTTTT[G/T]TGAGACGGAGTCTCG | 55626 |
rs78271057 | snp | G/T | 0.00835141 | 0.0640778 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46466842 | CCAGAGGCAATCACT[G/T]TTCAAACCTTTTTTT | 55626 |
rs78301726 | snp | A/T | 0.00993419 | 0.0697739 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46558265 | AACACTACTAACCTA[A/T]TATCACCGGGCGCAG | 55626 |
rs78383566 | snp | A/G | 0.111928 | 0.208413 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46423193 | AGAGTGGCAGTGGGA[A/G]AAATACCTTGGCCAT | 55626 |
rs78405538 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46553423 | CTGGAGTACTAAGAT[A/G]TAAAAGTCAGAAAGA | 55626 |
rs78447019 | snp | G/T | 0.0418186 | 0.138422 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46485365 | TCAAAAGATGAACGG[G/T]GACACATTTGCAGAG | 55626 |
rs78463585 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46585358 | TCAATAAAAATAAAT[A/T]AATAAATAAATAATT | 55626 |
rs78522042 | snp | A/T | 0.00676609 | 0.0577691 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46435850 | ACAACAGCACCAATG[A/T]GATGTTAACTGGCAC | 55626 |
rs78533782 | snp | G/T | 0.5 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46477336 | CTTTTTTTTTTTTTT[G/T]AGACAGGATCTTGCT | 55626 |
rs78538355 | snp | A/C | 0.5 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46564144 | AGCAAAACTCCGTCT[A/C]AAAAAAAAAAAAAAA | 55626 |
rs78591129 | in-del | -/AAA | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46547897 | GACAAAAAAAAAAAA[-/AAA]GTTAAAATACATGAT | 55626 |
rs78591608 | snp | C/T | 0.5 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46467551 | ACTCTATGTTACTCT[C/T]TTTTTTTTTTTTTTT | 55626 |
rs78594871 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46505303 | CTCCTCACAGAGCAC[A/G]TGGACACTCAGAGGA | 55626 |
rs78612907 | snp | C/G | 0.0410537 | 0.137264 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46410153 | ACACAAAAGATCAAG[C/G]AGGTGCTGCTCTGGT | 55626 |
rs78613375 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46488033 | ATATAAGAAAAAATT[C/G]ACTTTAAGACAAAAA | 55626 |
rs78627461 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46498204 | AGGGTGCTAAATACC[A/G]GGCTCTAACAACATA | 55626 |
rs78629321 | snp | A/G | 0.000543581 | 0.0164771 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46542722 | GGGGGCATGGATTCC[A/G]CCTCAGAGCGGGAGT | 55626 |
rs78632050 | snp | A/G | 0.0298908 | 0.118541 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46478481 | CAGAAATACAGGGCT[A/G]TATCCTAGAAAATAC | 55626 |
rs78714510 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46582833 | TTCTGATCAGAACCA[A/G]TATTTGCTAGATAAA | 55626 |
rs78789499 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46424139 | TTTAAAAAATCAAAA[A/T]AACAAGTCACCTAAC | 55626 |
rs78800354 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant, downstream-variant-500B | AMBRA1 | GRCh38.p7 | 11:46430598 | TAGCAATTAGCAATT[C/T]ATTTTCAGAAGAGTT | 55626 |
rs78805594 | snp | C/T | 0 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46531609 | CAGCTACTTGGGAGG[C/T]TGAGGCAAGAGAATC | 55626 |
rs78807356 | snp | G/T | 0.0150606 | 0.0854603 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46575120 | TTAAAAGTACCAGTG[G/T]TATCAGTAACTCCCT | 55626 |
rs78879884 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46594871 | TACCTTACCTGCTCC[C/T]AGGGAGGTTTACACC | 55626 |
rs78912304 | snp | A/G | 0.5 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46590470 | CCTCATCTCTTCAGG[A/G]AAAAAAAAAAATTAA | 55626 |
rs78916919 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46570613 | AAACCCTAGCTCAAC[A/G]TGATGTTACTTGCCC | 55626 |
rs78945435 | snp | C/T | 0.105924 | 0.204309 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46485391 | CAGAGCTTCTTCAAA[C/T]TGTACGAAAGACAAA | 55626 |
rs78957082 | snp | C/T | 0.0387552 | 0.1337 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46460904 | CCTGTCTGGGCAACA[C/T]AGTGAGACCACATCT | 55626 |
rs78977331 | snp | A/G | 0 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46405800 | GCAGTGGCATATCAC[A/G]GCTCACTGCAGTCGC | 55626 |
rs79001013 | snp | A/T | 0 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46500293 | TTAGCATTTTTTTTT[A/T]AGACAAGAAAAGTAA | 55626 |
rs79014257 | snp | C/T | 0.105214 | 0.203807 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46485969 | ATAGGTAAAAGGCCC[C/T]GGGTGCTATAAGGCA | 55626 |
rs79048336 | snp | A/T | 0 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46426072 | CTCCATCTCAAAATA[A/T]AAAAAAAAAAAAAAG | 55626 |
rs79078082 | snp | A/G | 0.067446 | 0.170804 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46464509 | CTTGGGTCTACAGAT[A/G]GGCTTCAGGTGGTTC | 55626 |
rs79154577 | snp | C/G | 0.0310518 | 0.120672 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46479941 | GGACTCATTGGGCTA[C/G]AAGAAAGGTGTTGGC | 55626 |
rs79174531 | snp | A/G | 0.5 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46564260 | TATGTATCCAATTAC[A/G]TATGAACTGATAAAG | 55626 |
rs79175840 | snp | A/C | 0 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46583680 | AAAAAAAAAAAAAAA[A/C]AACAAAACAACCCCA | 55626 |
rs79187162 | snp | G/T | 0.5 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46535851 | GCAGACCCTGAGTCA[G/T]CAGTGTAAAGCCAAT | 55626 |
rs79193955 | snp | A/G | 0.5 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46516944 | TCACTGAAGCTGAAG[A/G]AAAAAAAAATACAAA | 55626 |
rs79203530 | snp | C/T | 0.102014 | 0.201495 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46580054 | AGACCATCTCCACTT[C/T]GTCCCTTCCCATGCC | 55626 |
rs79221994 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46398230 | GCCTCAATGAGTTCT[C/T]TCAGCACCAGTGGCA | 55626 |
rs79261622 | in-del | -/AA | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46527506 | AAAAAAAAAAAAAGG[-/AA]CAACCTATGGAATGG | 55626 |
rs79313314 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46491210 | CTCCCTCTTATAAAG[A/T]CCTAAGAAAAAGAAT | 55626 |
rs79317058 | snp | A/C | 0.375 | 0.216506 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46583651 | AACTCAAACAAATTT[A/C]CAAAAAAAAAAAAAA | 55626 |
rs79325007 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46492725 | CATGCCTCACAGCCG[A/G]AAAACATCTGTCACT | 55626 |
rs79350465 | snp | A/G | 0.5 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46533168 | ACTCTGTCTCAAAAG[A/G]AAAAAAAAAAAGGAA | 55626 |
rs79357176 | snp | C/T | 0.0418186 | 0.138422 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46448859 | ATGCAATGGACTAAC[C/T]TTCCTTGAAAGACAC | 55626 |
rs79398446 | snp | A/G | 0.0916144 | 0.193427 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46528805 | GATAAAAAGGGTTAC[A/G]TGTGCCAACAGAACA | 55626 |
rs79402106 | snp | A/G | 0.0310518 | 0.120672 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46442524 | AGAAGCAGTCAAGCA[A/G]AGGCTGGACCATCCC | 55626 |
rs79413317 | in-del | -/TTA | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46532331 | TCAAGGTGGCAATTA[-/TTA]GAATAAAACAAAAGT | 55626 |
rs79445785 | snp | C/T | 0.197082 | 0.244335 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46569393 | TACCCTGCAGCCTAC[C/T]TTTTTCACCTATTAT | 55626 |
rs79446647 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46438819 | ACTTTTTTCAGGAAA[G/T]CAATTTCAAAATTAT | 55626 |
rs79447200 | snp | C/T | 0.039522 | 0.134904 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46408966 | TCACTCAGTCATGCC[C/T]TTCAACAACAGGCCC | 55626 |
rs79454270 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46462512 | CACTGAGGTAGACTC[A/G]TTGGTCTTCAAGGCC | 55626 |
rs79505812 | snp | A/G | 0.102014 | 0.201495 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46572832 | GGTATGGTGGCTCAC[A/G]CCTGTAATCACAGCA | 55626 |
rs79565082 | snp | A/T | 0.00874735 | 0.0655527 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46546431 | CTAGGACAAAGAGGA[A/T]CTTGCTTTGATGATC | 55626 |
rs79567606 | snp | A/T | 0.0298908 | 0.118541 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46468370 | TATAGTGAGACCTCA[A/T]CTCTTGAAAAAAAAG | 55626 |
rs79611418 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46562100 | GCTAGAAAGAAAATA[C/T]GGCAGGTGAAAGAAA | 55626 |
rs79642636 | snp | A/C | 0 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46558574 | AAAAAAAAAAAAAAA[A/C]CCACTACCTACCTAG | 55626 |
rs79669516 | snp | C/G | 0.0322114 | 0.122752 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46576722 | TTAACACCACCTGAA[C/G]AATATCCCTCCAAGA | 55626 |
rs79673815 | snp | A/T | 0 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46406376 | TATCTTTAAATTAAA[A/T]AAAAAAAAAAAAAAA | 55626 |
rs79751353 | snp | A/G | 0.5 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46477498 | GCTCAGCTAATTTCT[A/G]GAAAAAAAAAAAAAA | 55626 |
rs79777974 | snp | A/C | 0.0103295 | 0.0711199 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46476078 | GCACTCAGTGCCTGA[A/C]AACAATGACTGATGA | 55626 |
rs79796688 | snp | C/T | 0.0425829 | 0.139564 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46510806 | GCTCTGACCTATACA[C/T]AGTGTATAGGGTGAA | 55626 |
rs79803993 | snp | A/G | 0 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46447252 | TCGCAAAAAAAAAAA[A/G]GGCCACGCGCAGTAG | 55626 |
rs79810475 | snp | C/T | | | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46547151 | CCCCATCTAGGCAGC[C/T]AGAAGCAATAAGGCC | 55626 |
rs79825300 | snp | A/T | 0 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46557153 | AAAAAAAAAAAAAAT[A/T]AGCCAGGCATGGTGA | 55626 |
rs79858428 | snp | A/C | 0.5 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46556414 | ACATTCCCGAAGGCA[A/C]ACACACCTAGAAGCA | 55626 |
rs79879794 | snp | G/T | 0.5 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46460340 | TTTTTTTTTTTTTTT[G/T]AGACGGAGTCTCGCT | 55626 |
rs79893165 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46463388 | TCTTTATATAAAATA[C/T]ATAGATGCTCTGCTG | 55626 |
rs79899566 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46443434 | AATTTTTGAGTTCTG[A/G]CTCACCAGCAAATAT | 55626 |
rs79913909 | snp | A/C | 0.0345262 | 0.126772 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46444997 | ATGATACTTCTAGAT[A/C]ATGCATTCTCAACAT | 55626 |
rs79918375 | in-del | -/AA | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46526562 | TAAAAAAAAAAAAAA[-/AA]GCCTGGCTACTCTCT | 55626 |
rs79928554 | snp | C/T | 0.039522 | 0.134904 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46410627 | CAAGCCTAACCGGCT[C/T]CTCCTCGGAGCTAAG | 55626 |
rs79963008 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46540203 | ATTTCTCAGAATAGC[A/G]CATGAAGAGGTACTA | 55626 |
rs79967052 | snp | A/G | 0.0836354 | 0.186609 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46434319 | TCATTTGTTTAGTCA[A/G]CTCTTAAAAAAAAAA | 55626 |
rs80014291 | snp | C/T | 0.5 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46418556 | CCCTCCCCACTCCCC[C/T]TACCCCACAACAGGC | 55626 |
rs80015663 | snp | C/T | 0.0364509 | 0.129988 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46498750 | TCTGACTTGGGCCTT[C/T]ATAAATGAAGCTCTT | 55626 |
rs80028330 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46593525 | AAAGGAAGGAGGGTC[A/C]AAGTGCGCAAAGCTC | 55626 |
rs80031726 | snp | C/T | 0.226484 | 0.248892 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46459709 | GAGCAAGACTCCATC[C/T]CCCTCCCAAAAAGAA | 55626 |
rs80056236 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46429655 | TTCATCAGTAATTTT[C/G]TATTTTTGTTATTAT | 55626 |
rs80098617 | snp | C/G | 0.00336426 | 0.0408756 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46434889 | GCCCAGGTTATGGGG[C/G]GCCAGGGAGTACACT | 55626 |
rs80110861 | snp | C/T | 0.0387552 | 0.1337 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46465502 | TCTCAGAGAGTTCAC[C/T]GTTCTCTAAAGATTA | 55626 |
rs80110871 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46550717 | CAATAGCAAAAACTG[A/C]GGATAACCAAGTGTC | 55626 |
rs80138829 | snp | C/T | 0.00159617 | 0.0282053 | downstream-variant-500B | AMBRA1 | GRCh38.p7 | 11:46396066 | ATCCAGGTTTCTGGC[C/T]AGTTACATCACTTCA | 55626 |
rs80155985 | snp | A/C | 0.5 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46525750 | AGCAAGACTCCGTCT[A/C]AAAAAAAAAAAAATT | 55626 |
rs80179555 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46560963 | GGCTGGAGTAGGGCC[A/G]ATTTCAAATCATAAA | 55626 |
rs80208695 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46511108 | AGGAGGATAAATCAT[A/G]GTCGTTAAGTATCCT | 55626 |
rs80211369 | snp | G/T | 0.5 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46425310 | TTTTGCTTGATCCAT[G/T]TGTGTGTGTGTGTGT | 55626 |
rs80237103 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46430042 | CTGACTTACCCATCA[A/G/T]TAAAACTGGGAGGAC | 55626 |
rs80271229 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46506003 | TGAGAGAAAGTCACC[C/T]AGGCTTTTCAGCAGC | 55626 |
rs80278791 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46424140 | TTAAAAAATCAAAAT[A/G]ACAAGTCACCTAACT | 55626 |
rs80289660 | snp | A/C | 0.5 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46564147 | AAAACTCCGTCTCAA[A/C]AAAAAAAAAAAAAAA | 55626 |
rs111227408 | in-del | -/A | 0.0337553 | 0.125452 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46570912 | GGGATAGAGAACTGG[-/A]AAAAAAAATAAATGA | 55626 |
rs111298601 | snp | A/G | 0.00119737 | 0.0244387 | downstream-variant-500B | AMBRA1 | GRCh38.p7 | 11:46395913 | TAGAGCAGGCCTTTC[A/G]GCCACTGTAGGGAAG | 55626 |
rs111312158 | in-del | -/A | 0.5 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46525750 | GCAAGACTCCGTCTC[-/A]AAAAAAAAAAAAATT | 55626 |
rs111312716 | in-del | -/CACACACAAAAAAACG | 0.5 | 0 | intron-variant, upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46591865 | CCGTCTCAAAAAACA[-/CACACACAAAAAAACG]CTCTCTTACTGATTC | 55626 |
rs111328862 | snp | A/G | 0 | 0 | intron-variant, upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46592768 | CTTAAAAAAAAAAAA[A/G]AAAAAAGAGAGACAG | 55626 |
rs111360734 | snp | A/C | 0.0115144 | 0.0749975 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46502978 | AGGCAGGAGAATGGC[A/C]TGAACCTGGGAGGCG | 55626 |
rs111367204 | snp | A/C | 0.5 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46528709 | GAGATCTATTGAACA[A/C]TAATGTGTACTGTAC | 55626 |
rs111377053 | snp | C/G | 0.5 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46400533 | GTCTCGCTATGTCAC[C/G]TAAACTGGAGTGCAA | 55626 |
rs111377759 | snp | C/T | 0.5 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46467026 | GGATCCAGGCGATTC[C/T]CCTGTCTCAGCCTCC | 55626 |
rs111378257 | snp | G/T | 0.5 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46432207 | ACAAATAACTGCAGT[G/T]TGGTGTGACAAGTAC | 55626 |
rs111387831 | snp | G/T | 0.0314385 | 0.121371 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46471298 | AAATATAAAAATTCG[G/T]CTGGGCACGGTGGCT | 55626 |
rs111449703 | snp | C/T | 0.0020175 | 0.0316966 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46494215 | TGTCCCTGAAAAAAA[C/T]AAAAACACTACACAT | 55626 |
rs111449880 | snp | A/G | 0.287346 | 0.247195 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46406305 | TGATCTGCCCACCTC[A/G]GCCTCCCAAAGTTGC | 55626 |
rs111475696 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46524476 | AGACTAACCAAGAAA[A/C]CTCTGAGTAACTAAA | 55626 |
rs111482052 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46577776 | ACCAATATGGAGAAA[C/T]CCTGTCTCTACTAAA | 55626 |
rs111513238 | snp | C/T | 0.5 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46409805 | TTATCAACAACCCAG[C/T]GCTTTGTTCCAGTCT | 55626 |
rs111525722 | snp | A/G | 0.0298908 | 0.118541 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46532570 | GCCTCCCAAATAGCT[A/G]GGACTACAGGCACCC | 55626 |
rs111542162 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46422482 | GCTTGCCTCTCTACC[C/T]CTCAAACTCTAATAG | 55626 |
rs111565811 | in-del | -/A | 0.0298908 | 0.118541 | intron-variant, upstream-variant-2KB | AMBRA1, MIR3160-2 | GRCh38.p7 | 11:46449863 | CAGGAGTTTAAGACC[-/A]GCCTGACCAACATAG | 55626 |
rs111573205 | snp | A/G | 0.5 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46556136 | TAAAACTGCCCCAGT[A/G]CTCTTTGGAAACTCC | 55626 |
rs111581892 | snp | A/C | 0.0154538 | 0.0865337 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46522244 | AGTTATTTTTAATAC[A/C]TTTGTAAGATGACTG | 55626 |
rs111598350 | snp | A/G | 0.5 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46523712 | GCTTTATTTAGAAAA[A/G]TCAGAGACAAAAGAC | 55626 |
rs111600181 | snp | C/T | 0.0425829 | 0.139564 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46449748 | CACAAAATTGGAGGA[C/T]TGACACAACCCAACT | 55626 |
rs111617127 | snp | A/C | 0 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46488462 | AAAACAAAACAAAAC[A/C]AAAAAAAAAACTGAC | 55626 |
rs111629797 | snp | A/T | 0.5 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46408900 | CCCAAGGTTAGTCTA[A/T]ACCCTAGAACAATGA | 55626 |
rs111660556 | snp | A/C | 0 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46567200 | CCTCAGCCTCCCGAG[A/C]AGCTGGAATTACAGG | 55626 |
rs111667759 | snp | G/T | 0.0418186 | 0.138422 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46557899 | ATCACTTGAACCCAG[G/T]AGGTGGGGGTTGCAG | 55626 |
rs111677905 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46551128 | AAAGAATAGATGTCC[A/G]AAATATATTGTCGAG | 55626 |
rs111680500 | snp | C/G | 0.0422008 | 0.138995 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46540621 | CATACCATACCCTTT[C/G]CTCCCTTAACATGTG | 55626 |
rs111698982 | snp | C/T | 0.5 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46446900 | AACTTCAATTTTCCA[C/T]ATCTGCCAATGGGAT | 55626 |
rs111705135 | snp | A/G | 0.0310518 | 0.120672 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46473852 | AGACGGTGTTTCACC[A/G]TGTTAGCCACGATGG | 55626 |
rs111707177 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46526736 | CACCCCACACACACA[A/C]AAAAAAACCATGAAA | 55626 |
rs111710050 | snp | A/G | 0.0310518 | 0.120672 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46552410 | AAAAAAAAAAAGGCC[A/G]GGCACGGTAGCTCAC | 55626 |
rs111720421 | snp | C/T | 0.0337553 | 0.125452 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46586482 | ATTTGAACCTATATC[C/T]TTTTACTTTATTTTG | 55626 |
rs111752355 | snp | C/G | 0 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46587012 | TAGGTATATATACCT[C/G]TGATCTATTCTAGAG | 55626 |
rs111797924 | in-del | -/C | 0.0298908 | 0.118541 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46398384 | ACCCTATGGGTGTGG[-/C]CCAAAGGGAAACAGT | 55626 |
rs111807821 | snp | A/T | 0.0376037 | 0.131863 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46503181 | CATGTCTTGCTCACT[A/T]ATCATTTGTAGCTTT | 55626 |
rs111816575 | snp | G/T | 0.5 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46441464 | AGATTGCAGTACACC[G/T]AGATCATGCGACTGC | 55626 |
rs111916841 | snp | A/G | 0 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46511875 | TTCTTTTTTTTTTGA[A/G]ACAGAGTCTTGCTCT | 55626 |
rs111924211 | in-del | -/TGTT | 0.5 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46567065 | AAGCATATTAAGTAG[-/TGTT]TGTTTGTTTGTTTGT | 55626 |
rs111933477 | snp | A/G | 0.106278 | 0.204558 | intron-variant, upstream-variant-2KB | AMBRA1, MIR3160-1 | GRCh38.p7 | 11:46453071 | TCTCCCCTAAATACC[A/G]TACCCATTAACAGTC | 55626 |
rs111934995 | snp | C/T | 0.5 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46489132 | CAGGTTTGTTACATA[C/T]GTATACATGTGCCAT | 55626 |
rs111942470 | snp | C/T | 0.5 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46413689 | AGAGACAGTGTTTCG[C/T]CATGTTGGCCAGGCT | 55626 |
rs111946670 | snp | A/C | 0.5 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46444958 | TGTAAGGAAAAGTAC[A/C]AATAACAGTTCATTT | 55626 |
rs112036748 | snp | C/T | 0.5 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46421873 | TTCCACGGGGACTGG[C/T]TCTGTAAACCCAAAG | 55626 |
rs112060320 | snp | A/C | 0.0788843 | 0.182262 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46426039 | GTAGTCCCAGCTACT[A/C]GGGAGGCTGAGGCGA | 55626 |
rs112082125 | snp | A/G | 0 | 0 | utr-variant-3-prime, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46397045 | CCCAACAGGTGGACA[A/G]GGCAAAGCTGCCTCG | 55626 |
rs112092850 | in-del | -/A | 0 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46447240 | TGAGACTCTTATCGC[-/A]AAAAAAAAAAAAGGC | 55626 |
rs112141417 | snp | C/T | 0.5 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46543574 | GATTCAAAATAATCA[C/T]ATGGTATTAAATTTT | 55626 |
rs112144478 | snp | C/T | 0.0298908 | 0.118541 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46516518 | TCACTGCAAGCTCCG[C/T]CTCCTGGGTTCGAGC | 55626 |
rs112145742 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46471870 | TGTCCTCATGATCCA[C/T]CCACCTCGGCCTCCC | 55626 |
rs112154656 | snp | C/T | 0.5 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46513421 | AAACTCAACTGATCA[C/T]ATGTGATACGTACAT | 55626 |
rs112161113 | snp | G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46583299 | AACTGGCTAGCCATA[G/T]GTAGAAAGCTGAAAC | 55626 |
rs112164044 | snp | C/T | 0.5 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46549530 | ATCAAGACACTTTAA[C/T]CCTGCATATTTAATT | 55626 |
rs112198143 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46553170 | CTGGTCTCGAACTCC[A/T]GACCTCAGGTGATCC | 55626 |
rs112221009 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46506276 | GAGAGAACCATGACC[C/T]CTGCTCCATTTGCCA | 55626 |
rs112233553 | snp | C/T | 0.000182344 | 0.00954666 | synonymous-codon, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46548258 | TACCTTGCCCTCCCA[C/T]TTCATCCACCGGGTT | 55626 |
rs112246496 | snp | C/T | 0.5 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46556264 | ATATAGAACCAAAGT[C/T]CAAACTGTAAGCACC | 55626 |
rs112256056 | snp | C/T | 0.5 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46473916 | CAGCTTCCCAAAGTG[C/T]TGGGATTACAGGCGT | 55626 |
rs112277531 | snp | C/T | 0.0314385 | 0.121371 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46484891 | ACCTCATGATCCACC[C/T]GCCTCGGCCTCTGAA | 55626 |
rs112299227 | snp | C/T | 0.5 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46563902 | GTAATCTCAGCACTT[C/T]GGGAGGCTGGGGTGT | 55626 |
rs112323391 | snp | A/G | 0.5 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46544845 | GAGGCGGCCAGGTGC[A/G]GTGGCTCATACCTAT | 55626 |
rs112323696 | snp | A/G | 0.0901694 | 0.192235 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46538767 | CCTCTCAAAGTGCTG[A/G]GATTACAGGCGTGAG | 55626 |
rs112327359 | snp | C/T | 0.0298908 | 0.118541 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46567574 | CCATGTTGGCCAAGC[C/T]GGTCTCGAACTCCTG | 55626 |
rs112357959 | snp | C/G | 0.0418186 | 0.138422 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46459537 | CCAACATGGTGAAAC[C/G]CCGTCTCTACTAAAA | 55626 |
rs112360857 | in-del | -/T | 0.5 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46565938 | CATCACATCGGCTAA[-/T]TTTTTTTTGTATTTT | 55626 |
rs112409363 | snp | A/G | 0.0298908 | 0.118541 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46575271 | GAGATCGGCCTGACC[A/G]ACATGGTGTAATCCC | 55626 |
rs112419908 | snp | A/G | 0.202651 | 0.245475 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46531849 | CCAGCTGGGAGAGGT[A/G]GCTCACGCCTGTAAT | 55626 |
rs112460328 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46580136 | TTGCTATAATCATCA[A/G]TGATCTCTGTGCTGA | 55626 |
rs112578969 | snp | C/T | 0.093777 | 0.195178 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46488001 | ACAACCATAAAAGAA[C/T]TGCAGTAGCTATATT | 55626 |
rs112581658 | snp | C/T | 0.5 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46459751 | ACATACACACACACA[C/T]ACACACACACACACA | 55626 |
rs112609169 | snp | A/G | 0.030278 | 0.119257 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46515837 | TGCGCCACCACACCC[A/G]GCTAATTTTTGTACT | 55626 |
rs112660289 | snp | C/T | 0 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46583220 | CAACTATCTGATCTT[C/T]GACAAACCTGAGAAA | 55626 |
rs112675340 | snp | A/G | 0.5 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46512654 | AGAGGCACAGAACGG[A/G]GCTTCCAACAGTGTG | 55626 |
rs112698925 | snp | C/T | 0.00626953 | 0.0556368 | missense, intron-variant | AMBRA1 | GRCh38.p7 | 11:46518383 | TGCAGTGAGCCAAGA[C/T]AGCGCCGCTGTACTC | 55626 |
rs112705011 | snp | C/T | 0.198634 | 0.244666 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46567557 | GTAGAGATGGGGTTT[C/T]GCCATGTTGGCCAAG | 55626 |
rs112728012 | snp | G/T | 0.5 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46502959 | TCAGCTACTCAGGAG[G/T]CTGAGGCAGGAGAAT | 55626 |
rs112746390 | snp | C/T | 0.0337553 | 0.125452 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46572042 | GCGTGGTAGCTCACG[C/T]CTATAATCCCAGGAC | 55626 |
rs112748031 | snp | A/C | 0.0298908 | 0.118541 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46517369 | GCTGGAGCTGGTCTC[A/C]ATCTTCTGACCTCAG | 55626 |
rs112752165 | snp | C/T | 0.0298908 | 0.118541 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46441279 | AGCACTTTGGGAGGC[C/T]GAGGTGGGTGGATCA | 55626 |
rs112820516 | snp | A/G | 0.5 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46543667 | ACATCTCCCCATGAC[A/G]TGGAAGCAGTGAGGG | 55626 |
rs112831686 | snp | A/G | 0.5 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46508019 | AACTGCCAGAGGTGG[A/G]AGTGCTCTGGGCATC | 55626 |
rs112852286 | snp | C/T | 0.5 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46410097 | AGCAGAGCTTTTGTT[C/T]TCTTTCTTAGCCACA | 55626 |
rs112897300 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46565956 | TTTTTTGTATTTTTC[A/G]TAAAGACAGATTGCC | 55626 |
rs112899549 | snp | G/T | 0.0142736 | 0.0832652 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46575277 | GGCCTGACCAACATG[G/T]TGTAATCCCATCTCT | 55626 |
rs112900064 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46512136 | GATGGGATTACAGGC[A/G]TGAGCCACCATGCCC | 55626 |
rs112915728 | snp | A/G | 0.030278 | 0.119257 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46532626 | ATTTTTAGCAGAGAT[A/G]GGGTTTCACCATGTT | 55626 |
rs112937161 | in-del | -/ACGTATTTGCAGCAC | 0.0130921 | 0.0798413 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46530171 | GGGAAATTACTCCCA[-/ACGTATTTGCAGCAC]ACATACAGACGTCAC | 55626 |
rs112946135 | in-del | -/T | 0.329783 | 0.236927 | upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46595241 | AGACCCTATCTTAAA[-/T]TTTTTTTTTTTTAAA | 55626 |
rs112958863 | snp | A/G | 0.5 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46465400 | TCCTTACCATATTGG[A/G]ATAAAAACAAAATCC | 55626 |
rs112959855 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46533116 | TGCAGTGAGCCAAGA[C/T]TGCACCACTGCACTC | 55626 |
rs112982888 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46587939 | CCTCAGAAAAAAACA[C/T]GGTACCAAAACAACA | 55626 |
rs112987436 | snp | A/C | 0.5 | 0 | intron-variant, upstream-variant-2KB | AMBRA1, MIR3160-1 | GRCh38.p7 | 11:46453127 | TGCCCTAGCCCTAGG[A/C]AATCACTAATTGCTT | 55626 |
rs113039520 | snp | A/G | 0.021333 | 0.101051 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46515023 | ATGGAAGCAAGGTCT[A/G]GGAGCAGCTGACTAT | 55626 |
rs113053306 | in-del | -/ACAA | 0.030665 | 0.119967 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46445382 | GGTGTGCTGTCAGTG[-/ACAA]AGTCCACTGACCTCA | 55626 |
rs113073011 | snp | A/G | 0.5 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46493434 | AAACATTTTTCTTCA[A/G]CCCTGCCATTTCCTG | 55626 |
rs113115425 | snp | C/T | 0.5 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46549726 | AGCAACGACTTTGGA[C/T]GTTTATGTCTCTTTA | 55626 |
rs113118060 | snp | C/T | 0 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46585719 | ATATATATATATATA[C/T]ATATTCCTAGCTTCC | 55626 |
rs113130368 | snp | A/C | 0 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46582376 | AGTTTAATTCAGGTT[A/C]CCCTACTATAATCTC | 55626 |
rs113137464 | snp | A/G | 0.0425829 | 0.139564 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46568445 | CTTGGGTGACAAGAG[A/G]GAAACTCAAAAACAA | 55626 |
rs113142628 | snp | A/T | 0 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46554422 | AGAGTAGCTACAAAT[A/T]TCAATACCAAGAAAA | 55626 |
rs113179649 | snp | C/G | 0.5 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46475171 | CCCTAGTCAGCCTAT[C/G]TGGCAGGCAGCCTCC | 55626 |
rs113182863 | snp | C/T | 0.5 | 0 | intron-variant, downstream-variant-500B, upstream-variant-2KB | AMBRA1, MIR3160-1, MIR3160-2 | GRCh38.p7 | 11:46451350 | AATCATAATAATCAT[C/T]ACAGTCACATGATAG | 55626 |
rs113206642 | in-del | -/TTT | 0.5 | 0 | intron-variant, upstream-variant-2KB, downstream-variant-500B | AMBRA1, MIR3160-1, MIR3160-2 | GRCh38.p7 | 11:46452332 | TTTGTTATTTTAAGG[-/TTT]TTTTTTGTTGTTGTT | 55626 |
rs113211612 | in-del | -/AA | 0.0298908 | 0.118541 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46553744 | GTGAGACTCCATCTC[-/AA]AAAAAAAAAACACAA | 55626 |
rs113236040 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46572687 | CAGCTAGTATTTTGG[A/G]GTGTTTACTCTGAAC | 55626 |
rs113238967 | in-del | -/T | 0.5 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46400655 | ACCACTCCTGGCTAA[-/T]TTTTTGTACTTTTTG | 55626 |
rs113262475 | snp | A/G | 0.0425829 | 0.139564 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46568900 | CAACCTCCGCCTCCC[A/G]GGTTCAATCGATTCT | 55626 |
rs113291219 | snp | A/G | 0.0298908 | 0.118541 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46575231 | GGGAGGCTGAGGCAG[A/G]TGTATCACCTGAGGT | 55626 |
rs113305101 | in-del | -/AGAAC | 0.0295035 | 0.117819 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46439361 | ATCAGACAGATCACT[-/AGAAC]AGAACAGAGAGTCCA | 55626 |
rs113314955 | snp | C/T | 0.0298908 | 0.118541 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46568214 | TGTAATCCCAGCACT[C/T]TGGGTGGCCGAGGCA | 55626 |
rs113317338 | snp | A/T | 0.5 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46466594 | CAAAGGCTTATATAA[A/T]TAATAATAGAGATCA | 55626 |
rs113318629 | snp | A/G | 0.5 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46427009 | AATACTCTGGATTGA[A/G]CTAGAATTCTAGGTC | 55626 |
rs113338110 | snp | A/G | 0.030278 | 0.119257 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46567581 | GGCCAAGCCGGTCTC[A/G]AACTCCTGGCCTCAA | 55626 |
rs113338170 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46412943 | ACTTGTCAAGATGTA[C/T]TGACAGGTTGCAATA | 55626 |
rs113370226 | snp | G/T | 0.0170251 | 0.090679 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46587863 | TCTTCATAGGTAAGG[G/T]TTGAAACACACAGTC | 55626 |
rs113397161 | snp | C/G | 0.5 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46574812 | CTCTACCATTTGCCA[C/G]CTGTATAACCTTTGA | 55626 |
rs113402465 | snp | A/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46400501 | TTTTTTTTTTTTTTT[A/T]TTTTTTTTGAGACCA | 55626 |
rs113423810 | snp | C/T | 0.5 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46544412 | ATATGGCAGCTACAC[C/T]GGCAAGAAGCATGAA | 55626 |
rs113425036 | snp | A/G | 0.0825414 | 0.185628 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46514441 | CACTGAACAGAGAGA[A/G]CACAATGTAAACAAG | 55626 |
rs113434992 | snp | C/T | 0.5 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46455277 | AAGTGTACAGTTCAG[C/T]AGAACTGTATGTATG | 55626 |
rs113438042 | snp | C/T | 0.5 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46417530 | TTAAGTTAAAGTCTA[C/T]GGTATTTACTCAAAC | 55626 |
rs113443490 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46516484 | TGCCCAGGCTGGAGT[A/G]CAGTGGCACGATCTC | 55626 |
rs113446918 | snp | C/T | 0.0792508 | 0.182605 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46568107 | AAGCTGAGATCCTGC[C/T]GCTGCACTCCAGCCT | 55626 |
rs113495508 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46532131 | CTCAGAAATAAATTA[A/G]TTAATTAATTAATAT | 55626 |
rs113514757 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46402417 | CCCAGGCTGGAGTGC[A/G]GTGGCGAGATCTCAG | 55626 |
rs113531907 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46583037 | CAAATGAATGACTGT[C/T]GCCAAGTCAATCCTA | 55626 |
rs113533721 | snp | A/T | 0.5 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46554581 | TCTCTCTTTCATCTG[A/T]AGAAAAATATTTGCT | 55626 |
rs113539602 | snp | C/T | 0.5 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46426416 | TTTTGTTCACTGCTG[C/T]ATTCCTAGACCAATG | 55626 |
rs113550513 | snp | C/T | 0.5 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46399015 | CTGACCTCAGGTGAT[C/T]CACCCTCCTCGGCCT | 55626 |
rs113572880 | in-del | -/T | 0.5 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46589787 | ACCATTCCCCGCTAA[-/T]TTTTTTTGTATTTTT | 55626 |
rs113627815 | snp | C/T | | | intron-variant, upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46592682 | GGAATCGCTTGAACC[C/T]GGGAGGCAGAGGTTG | 55626 |
rs113658126 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46516489 | AGGCTGGAGTGCAGT[A/G]GCACGATCTCGGCTC | 55626 |
rs113705973 | snp | C/T | 0.030278 | 0.119257 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46567607 | CTCAAGTGATTCGCC[C/T]GCCTCAGCCTCCCAA | 55626 |
rs113728549 | snp | A/C | 0 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46541762 | GCCAACTGACTCATA[A/C]TGCTAGGCCCTATCC | 55626 |
rs113794943 | in-del | -/C | 0 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46571729 | AGTGTCCCTCTGTCG[-/C]CCCAGGCTGGAGTGC | 55626 |
rs113838489 | snp | C/T | 0.0437281 | 0.141251 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46551706 | CAAAACCTACTCTAC[C/T]AAAAATACAAAATTT | 55626 |
rs113871254 | snp | A/G | 0.5 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46567780 | AGGACCATTTCACAT[A/G]TGCCTATGATTGCAA | 55626 |
rs113883754 | in-del | -/CAAT | 0.0298908 | 0.118541 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46543485 | AAAACTAACCACTGA[-/CAAT]CATCCAAGGAAAACA | 55626 |
rs113891937 | snp | A/C | 0.00809703 | 0.0631106 | missense, intron-variant | AMBRA1 | GRCh38.p7 | 11:46518352 | GGAGAATGGCATGAA[A/C]CTGGGAGGCGGAGCT | 55626 |
rs113950773 | snp | A/G | 0.0298908 | 0.118541 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46587174 | CACCTAAAGTCAGGA[A/G]TTCGAGATCTGCCTG | 55626 |
rs113953350 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46470689 | ATTGCTTGAGCCCAG[A/G]AGTTGGGTGCTTGCA | 55626 |
rs113981669 | snp | A/G | 0.5 | 0 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46492110 | ACACAGAAGTGCCAG[A/G]CAAGGAGAGGCACGG | 55626 |
rs113999970 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46536489 | GAGAGATTAGATATC[A/G]AAACTCTTTAGACTC | 55626 |
rs114012541 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46434505 | CTTTGTATAGTTTTC[C/T]GATTATTTCCTTAAA | 55626 |
rs114014123 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46530566 | CATCAAAGAATCCCA[C/T]AAGAGCCAATACTTA | 55626 |
rs114016381 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46545037 | AAGACTGAGGTGGGA[A/G]GATTGCTTGGGCCCA | 55626 |
rs114032209 | snp | C/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46411201 | CTGAGCGGAGGAAGA[C/G]AAACTTCACCAAAAG | 55626 |
rs114045375 | snp | A/G | 0.0154538 | 0.0865337 | missense, intron-variant | AMBRA1 | GRCh38.p7 | 11:46518148 | AGAAGAATTACTCAC[A/G]GCCAGGCGCGGTGGC | 55626 |
rs114050866 | snp | A/G | 0.0414363 | 0.137845 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46568958 | ACTACAGGCATGTGC[A/G]ACCAAGACCAGCTAA | 55626 |
rs114070111 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46557380 | AATAAAAAGTTTAGG[A/C]CACAAAGCCCTGTAA | 55626 |
rs114101563 | snp | C/G | 0.00835141 | 0.0640778 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46529162 | GGTGCTCTGCAAAAG[C/G]TGCAGGCATTCTTCT | 55626 |
rs114121345 | snp | C/G/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46503562 | GTGCCAACTGCTCAA[C/G/T]GTCGGGTTGCCACAA | 55626 |
rs114177937 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46405510 | GCTTGCTTGAAGCTA[A/G]GAGTTCAAGACCAGC | 55626 |
rs114209492 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46412301 | CAAATAGTTATTATA[C/T]TGTATTGCATCTCAC | 55626 |
rs114266792 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46565017 | ATCCCACCACTTTAG[A/G]AGGCCAAGGCTTGAA | 55626 |
rs114328254 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46416128 | AAGAAAGGCCTGTAA[C/T]TGAAGTGTAAGTAAG | 55626 |
rs114332783 | snp | C/T | 0.0310518 | 0.120672 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46467411 | TAAATTCGTATTTCC[C/T]TTCACATGCAATTTT | 55626 |
rs114370180 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | AMBRA1, MIR3160-1 | GRCh38.p7 | 11:46453349 | CAGCTCACTGCAGCC[C/T]TGAACTACTGGGCTC | 55626 |
rs114473139 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46549638 | CTTCAATTATCATTC[A/G]AATTTTCCCCATTGT | 55626 |
rs114499737 | snp | A/G | 0.0425829 | 0.139564 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46501446 | GGATAGGCTCCAGCC[A/G]CCTGTGAGCCAGAAT | 55626 |
rs114530516 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46586124 | TAATAATGATTTTTA[A/G]AACTGGACGCACTGG | 55626 |
rs114560741 | snp | A/G | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46492579 | GGCAGTGGAGGTGGG[A/G]GGGAGGTAGGGAAAG | 55626 |
rs114618008 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46578553 | ATAAATATGGCTAAT[G/T]AGACTCTGGGCAAAG | 55626 |
rs114701128 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46430157 | GAAAAGACTCCAGCA[C/T]ATACAGCTATTCAAG | 55626 |
rs114817824 | snp | C/T | 0.039522 | 0.134904 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46400677 | TACTTTTTGCAGAGA[C/T]GGTTTCGCCGTGTTG | 55626 |
rs114858150 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46577497 | GCTTAACTGGTAAGG[G/T]GTTTTACTTTGCAGA | 55626 |
rs114880741 | snp | A/G | 0.039522 | 0.134904 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46578358 | CAGGCGTGGTCATGT[A/G]CGCTTGTAATCCCAG | 55626 |
rs114894179 | snp | A/G | 0.0414363 | 0.137845 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46536476 | CCAAAGAAACTGGGA[A/G]AGATTAGATATCGAA | 55626 |
rs114950537 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46513522 | TCACCACAACCTAGA[A/C]AGGTAGGTATGACTA | 55626 |
rs114996161 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46468193 | ATAGATGATAAAGAA[C/T]ATGCAGCAAGCAGTG | 55626 |
rs115161104 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46434339 | TAAAAAAAAAACAAA[A/G]AACACTTAAATTCAA | 55626 |
rs115213649 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46405811 | TCACAGCTCACTGCA[A/G]TCGCCACCTTCCAGG | 55626 |
rs115226706 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46556465 | TGAATTGTGTATCTA[C/T]TGTGTGCAAAAGATA | 55626 |
rs115249405 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46476725 | CAGAATCCAGAAAAA[C/T]ATTTAGACCAAGAAA | 55626 |
rs115292163 | snp | G/T | 0.0134861 | 0.0810011 | intron-variant, upstream-variant-2KB, downstream-variant-500B | AMBRA1, MIR3160-1, MIR3160-2 | GRCh38.p7 | 11:46452336 | GTTATTTTAAGGTTT[G/T]TTGTTGTTGTTGTTG | 55626 |
rs115301577 | snp | A/C | 0.0115144 | 0.0749975 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46537618 | CACCACTCAAGTTGC[A/C]ATGTAGCGTCAGACT | 55626 |
rs115413079 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46514371 | ACTATCAAGTAATGT[C/T]TTCTCTCTAGACAAG | 55626 |
rs115425595 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46490722 | GCAAAAGTTCCACTT[A/G]TGTCTGGAGTAAGAC | 55626 |
rs115427912 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46438982 | TGCTGAACTCATCAG[C/T]AAAACACAGAATCAG | 55626 |
rs115472122 | snp | G/T | 0.0150606 | 0.0854603 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46503566 | CAACTGCTCAATGTC[G/T]GGTTGCCACAAACCT | 55626 |
rs115495577 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46525678 | ATCATTTGAATCCGG[A/G]AGGCGGAAGTTGCAG | 55626 |
rs115529587 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46445103 | AAAAAAACTTAGTGT[A/T]ATCATTTGTTCCCCT | 55626 |
rs115631020 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46510303 | CCCTGTTCCCATGCA[C/T]TTTGCAAGGATGAAC | 55626 |
rs115672488 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46519016 | AAGAAAAGAACCTTC[A/G]CTTCATTATTTTATT | 55626 |
rs115684996 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46456937 | CAGCACATGACAAGA[C/G]AGTTAAAGCAAGAAA | 55626 |
rs115741598 | snp | A/G | 0.039522 | 0.134904 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46551736 | TACTCTACTAAAAAG[A/G]CAAAAATTAGGCCAG | 55626 |
rs115747504 | snp | G/T | 0.00131911 | 0.0256479 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46543943 | AAAGAACTCACAGTT[G/T]AGCTGGAATTGGAAC | 55626 |
rs115845226 | snp | A/C | 0.00835141 | 0.0640778 | intron-variant, upstream-variant-2KB | AMBRA1, MIR3160-2 | GRCh38.p7 | 11:46450531 | GGAAGCCTCAATTTT[A/C]TGGGCTCAGATGATC | 55626 |
rs115848873 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46531031 | TGGGAAAACAGGTGC[C/T]TGCCACCATGTCAGC | 55626 |
rs115851790 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46428272 | GATTTGTCTGGGTAA[C/T]ACTCACTCAACTCTT | 55626 |
rs115877937 | snp | C/T | | | intron-variant | AMBRA1 | GRCh38.p7 | 11:46541036 | GAGAAATTTCAGTTG[C/T]TTCGACAGAGGATGT | 55626 |
rs115952800 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46419236 | TCTAAGTATGTAGGG[C/T]TTGGGCTGAAGGTAA | 55626 |
rs115961727 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46481040 | CAACTTAATGTCCTC[C/T]TGGCTCTTTTGGCTG | 55626 |
rs116030238 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46537948 | AAAAGAACCAACCTC[A/G]TACACAAACAGCAGG | 55626 |
rs116039343 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46472791 | TTATCTGGTGGCCTT[C/T]GGAACTATGTCACTG | 55626 |
rs116040948 | snp | A/T | 0.00716266 | 0.059414 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46562973 | ACCTAATTTTTTATA[A/T]TTTTAGTGGAAACAG | 55626 |
rs116134193 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46474560 | CGCCTGGCTGACTTC[A/G]TATTTTTAGTAGAGT | 55626 |
rs116242611 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46448526 | ACGAAAGATCTAAAA[C/T]CTGTAATTTAAGCAC | 55626 |
rs116263221 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46538435 | ACCACAATGCATATA[C/T]TTTTTGGCACCAGAA | 55626 |
rs116389159 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46562666 | GCGGGTGGGGGAGCA[A/G]ATTAAAGGGATAAAT | 55626 |
rs116391569 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46498476 | GGAAGGAGTAGGGGG[A/G]AAAATACTTTCTTAT | 55626 |
rs116404642 | snp | A/G | 0.0383715 | 0.133092 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46507536 | CCTGGGGCTGACCCT[A/G]CTCCTTTAGCGCATC | 55626 |
rs116483398 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46580025 | GCCTACACATGTCAA[C/T]AATCAAAATACACAG | 55626 |
rs116484253 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46502015 | TTTTGTAAAGACATT[C/T]GACCACTACAAAAAT | 55626 |
rs116498699 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46523407 | CTAAAGTACAATTAG[C/T]AGAGAAACTGCAATT | 55626 |
rs116520914 | snp | A/G | 0.135484 | 0.22223 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46582134 | AAAAAAAAAAAATTC[A/G]AAAGCCTTGACATAG | 55626 |
rs116643004 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46401228 | GTGCACTGTGCCAGG[C/T]GCTGTGCCTAGTGAA | 55626 |
rs116755720 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46461021 | GCTGAGGCGGGAGGA[A/C]CCCTTGAGCTCAGGA | 55626 |
rs116792388 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46492734 | CAGCCGAAAAACATC[A/T]GTCACTAAGCTATTC | 55626 |
rs116807427 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46514720 | CCTCAAGTGATCCTC[C/T]TGCCTCGGCCTCCCA | 55626 |
rs116843384 | snp | A/G | 0.0193772 | 0.0965046 | upstream-variant-2KB | AMBRA1 | GRCh38.p7 | 11:46594872 | ACCTTACCTGCTCCT[A/G]GGGAGGTTTACACCC | 55626 |
rs116888818 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46437383 | ACTGCAATGAGCTCA[C/T]AGAGATATGCAAAGG | 55626 |
rs116917714 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46476382 | TTTCACTTAGATGGT[G/T]TATTTTTAGGGGTGG | 55626 |
rs116919080 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46414252 | TGCCTGGTGTCTCTG[C/T]AGCGCGGGAAAGAGC | 55626 |
rs116926294 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46439848 | ACACAAATGGCTGTG[C/T]ATATGAAGAGGCATG | 55626 |
rs116977134 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46572789 | TACATTTGTGGTCAC[C/T]AGATTTAAAAATAAG | 55626 |
rs117021349 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46412868 | CTCTGTTTTTGGTGA[A/G]CAAATCCTGTCTGTG | 55626 |
rs117023752 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46480199 | CTCAAGATCTATAAT[C/G]TTAATCATAACTGCA | 55626 |
rs117032845 | snp | A/C | 0.0788843 | 0.182262 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46515498 | AACAAACAAACAAAC[A/C]AACAAAAATACATCC | 55626 |
rs117051584 | snp | G/T | 0.00914312 | 0.0669923 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46442130 | TGTACGCCACCATGC[G/T]CAATTAATTGTGTGT | 55626 |
rs117082751 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46551368 | CCCAGGCTGGAGTGC[A/G]ATGGTGCAATCATGG | 55626 |
rs117100314 | snp | A/T | 0.0142736 | 0.0832652 | utr-variant-3-prime, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46396874 | CTTACCCCACAGTAG[A/T]CCCCCATTAGTAAAT | 55626 |
rs117105335 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46433321 | CAAATGAAGCCTGCT[G/T]GTCATGGATGGGCTT | 55626 |
rs117147261 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant, upstream-variant-2KB | AMBRA1, MIR3160-2 | GRCh38.p7 | 11:46450800 | TACAATGTTGGATAC[A/T]TGGCACATACATTTG | 55626 |
rs117148611 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46407360 | CTCCATTGAGAAGCC[C/T]GTGGTGGTTCCCTTT | 55626 |
rs117152017 | snp | C/G | 0.00953873 | 0.0683987 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46402237 | ACGTGGGTTTACACT[C/G]GGCGTGTATTTGTCA | 55626 |
rs117178898 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46471956 | CTTCAGGATTTGTTG[C/T]CTCGTTTCACATCCA | 55626 |
rs117222671 | snp | C/T | 0.0165278 | 0.0893908 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46545946 | GGTAGTGCCACTAAT[C/T]TATCAGATAAATACT | 55626 |
rs117266228 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46545512 | TTGCCCTGAGCAGGG[A/G]TAACAACCTGACTTC | 55626 |
rs117356785 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46484237 | GGTTTTGACCTCACA[A/T]TTGGCCTTCTCTTTC | 55626 |
rs117359589 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46557872 | AGCTACTGGAGAGGC[C/T]GAGGCAAGAGAATCA | 55626 |
rs117376578 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46579729 | TTGTTTTGTTTTGTT[C/T]TGAGATGGATTCTTG | 55626 |
rs117377924 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46415201 | ACTTCCCTATTTGTT[C/T]TCCTCATTTGAGACT | 55626 |
rs117386288 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46446020 | GACTCCCAAATCCCG[C/G]CTCCAGAGGCATCCT | 55626 |
rs117396687 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46580019 | CGCCCAGCCTACACA[A/G/T]GTCAATAATCAAAAT | 55626 |
rs117425994 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46409622 | AATGCTAGCATCCCC[C/T]TTCCTTGGGCATCTC | 55626 |
rs117427739 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46526204 | AGAGCGAAACATCGG[C/T]TCAAAAATAAATAAA | 55626 |
rs117438791 | snp | C/T | 0.000350816 | 0.0132395 | missense, nc-transcript-variant | AMBRA1 | GRCh38.p7 | 11:46397676 | CGGGGGCTTAGGCCT[C/T]GCTCTGCCAGTTGCC | 55626 |
rs117447018 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46465207 | TACTTAGCCTCACCC[A/T]TCCCTTCCCCTAGAA | 55626 |
rs117528979 | snp | C/G | 0.0111196 | 0.0737302 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46512902 | GGGAGAGATATATAA[C/G]TTTCCCCTTTTGCAG | 55626 |
rs117574045 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46449147 | GCAAGGAAGCCCCTT[C/T]TTACCAATACTTTTC | 55626 |
rs117580788 | snp | A/C | 0.0111196 | 0.0737302 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46515962 | TACAGGTGTGAGCCA[A/C]TGTGCTGGCCTTAAT | 55626 |
rs117653287 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46575918 | TAAAGAATTAAGAAT[C/T]CATTGCCGTGGTCTA | 55626 |
rs117659675 | snp | A/G | 0.0376037 | 0.131863 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46548972 | CTCCAGTGCCTGGGC[A/G]ACAGAGCAAGACTCC | 55626 |
rs117674325 | snp | C/G | 0.0142736 | 0.0832652 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46413467 | CCCTCTCTGGCTACT[C/G]AAACTCTTAGCTTTC | 55626 |
rs117690052 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46441048 | ATTCACTACTTTTTG[C/T]TAACAATCTGACAGA | 55626 |
rs117749211 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46442289 | CTGGGAAAACAGGCA[G/T]GCACCACCACACTCA | 55626 |
rs117769389 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46529935 | TCCTGGGCCCACCCC[C/G]CAACCACTCAATAAA | 55626 |
rs117908706 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46427741 | AGGCCGGGAGCGCTG[A/G]CTCATGCCTGTAATC | 55626 |
rs117925059 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | AMBRA1 | GRCh38.p7 | 11:46554388 | AACCTCAGATTCCTA[A/C]AGGATTCAGAAAGGG | 55626 |