SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs1136062 | snp | A/G | 0.311614 | 0.242289 | intron-variant | CCNF | GRCh38.p7 | 16:2452640 | GAAAGTGAAAATGTC[A/G]TCAATTTGATTGTTG | 899 |
rs1802723 | snp | A/T | | | utr-variant-3-prime, intron-variant | CCNF, LOC105371050 | GRCh38.p7 | 16:2457683 | GATGGCGTCAATGTG[A/T]ACACCTCTCTTTGTG | 899 |
rs3810795 | snp | A/G | 0 | 0 | utr-variant-3-prime, intron-variant | CCNF, LOC105371050 | GRCh38.p7 | 16:2457928 | CTCAGATGTTACAGA[A/G]GACTTGAAGTTTTTT | 899 |
rs4305017 | snp | C/T | 0.311369 | 0.242351 | intron-variant | CCNF | GRCh38.p7 | 16:2435191 | gggaggcggagcttg[C/T]agtgagccgagattg | 899 |
rs4306510 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | CCNF | GRCh38.p7 | 16:2434950 | ataattcgtATTTGA[C/T]TACATGTTATTAAGA | 899 |
rs4354939 | snp | A/G | 0.313082 | 0.241911 | intron-variant, upstream-variant-2KB | CCNF, MIR6767 | GRCh38.p7 | 16:2444504 | atggggtttcatcgt[A/G]ttagccaggatggtc | 899 |
rs4354942 | snp | C/T | 0.313082 | 0.241911 | intron-variant, downstream-variant-500B | CCNF, MIR6767 | GRCh38.p7 | 16:2445928 | AGAGACGGGGTTTCA[C/T]CATGTTGGTCAGGCT | 899 |
rs4371158 | snp | A/G | 0.31721 | 0.240796 | intron-variant | CCNF | GRCh38.p7 | 16:2446075 | TGTCCCACCTGGTCA[A/G]ACATGGAGTGCCACG | 899 |
rs4387603 | snp | C/T | 0.313082 | 0.241911 | intron-variant | CCNF | GRCh38.p7 | 16:2436614 | GGAGCCGAGGTCCTA[C/T]CCCTACCCTCCCATC | 899 |
rs4412969 | snp | C/T | 0.355096 | 0.226837 | upstream-variant-2KB, intron-variant | CCNF | GRCh38.p7 | 16:2428252 | CTGTGATCACCTGTT[C/T]ACTCTGTCTCTTGCC | 899 |
rs4494541 | snp | C/T | 0.311614 | 0.242289 | intron-variant | CCNF | GRCh38.p7 | 16:2435067 | ccatcctggctaaca[C/T]ggtgaaaccccgtct | 899 |
rs4534842 | snp | A/G | 0.31014 | 0.242659 | intron-variant | CCNF | GRCh38.p7 | 16:2435262 | ctcaaaaaaaaaaaa[A/G]aaaagaaaagaaaaa | 899 |
rs4542665 | snp | A/C | 0.312837 | 0.241974 | intron-variant | CCNF | GRCh38.p7 | 16:2446143 | TTCAGCGTGTGGGGG[A/C]CGCTGTGTGGGGTGC | 899 |
rs4544244 | snp | C/G | 0.315758 | 0.241197 | intron-variant | CCNF | GRCh38.p7 | 16:2446424 | GTGGGTGTCTCTCAG[C/G]AGCAGCGTGCGTCCT | 899 |
rs4578647 | snp | G/T | 0.298651 | 0.24522 | upstream-variant-2KB, intron-variant | CCNF | GRCh38.p7 | 16:2428186 | CCGGGACAGGGAATA[G/T]TCCCAACTTCCAGAC | 899 |
rs4589553 | snp | A/G | 0.00835909 | 0.0641067 | intron-variant, missense | CCNF | GRCh38.p7 | 16:2433009 | CACGCCAGTGTGTGG[A/G]CATGTGCCAGCTTCC | 899 |
rs4602040 | snp | G/T | 0.312348 | 0.242101 | intron-variant | CCNF | GRCh38.p7 | 16:2435144 | tggtcccagctactc[G/T]ggaggctgaggcagg | 899 |
rs4786282 | snp | A/G | 0.312837 | 0.241974 | intron-variant, upstream-variant-2KB | CCNF, MIR6767 | GRCh38.p7 | 16:2444019 | CCGCCTCCTGGGTTC[A/G]AGCAATTCTCCTGCC | 899 |
rs4786283 | snp | C/T | 0.359364 | 0.22481 | intron-variant, upstream-variant-2KB | CCNF, MIR6767 | GRCh38.p7 | 16:2444163 | TGACCTCGTGATCCG[C/T]CCGCTTTGGCCTCCC | 899 |
rs6600206 | snp | A/T | 0.309648 | 0.24278 | upstream-variant-2KB, intron-variant | CCNF | GRCh38.p7 | 16:2428549 | ACAGCTCAGATGGGC[A/T]CTGCCCAAGACAAGA | 899 |
rs7194278 | snp | C/T | 0.0271762 | 0.113356 | intron-variant | CCNF | GRCh38.p7 | 16:2452835 | tttccctcgcggtaa[C/T]gtttgctgggtttgt | 899 |
rs7201859 | snp | C/T | 0.359364 | 0.22481 | intron-variant | CCNF | GRCh38.p7 | 16:2439105 | gattttgagaccagc[C/T]tggccaacatggtga | 899 |
rs8052046 | snp | A/C | 0.311859 | 0.242226 | intron-variant | CCNF | GRCh38.p7 | 16:2434782 | cccacaatcctggaa[A/C]ctctagacaacccct | 899 |
rs8060813 | snp | C/T | 0.400522 | 0.199607 | intron-variant | CCNF | GRCh38.p7 | 16:2449010 | TTTTCCTTATTAATC[C/T]TCGTTGTCGCTGTGC | 899 |
rs9673516 | snp | G/T | 0.368324 | 0.220226 | intron-variant | CCNF | GRCh38.p7 | 16:2435598 | TCAGAGAGAGAGAGA[G/T]ATATATATATATATG | 899 |
rs9931062 | snp | A/G | 0 | 0 | intron-variant | CCNF | GRCh38.p7 | 16:2455273 | ATCTTCTTCGTAGCA[A/G]AACCTTTGGGAGCAC | 899 |
rs9934102 | snp | C/T | 0.0322114 | 0.122752 | intron-variant | CCNF | GRCh38.p7 | 16:2433179 | TGTTGCTGTCTCCCA[C/T]GACATTGCCTCATAC | 899 |
rs9936014 | snp | C/G | 0.0244596 | 0.10785 | intron-variant | CCNF | GRCh38.p7 | 16:2431103 | AATTTTTCATCTTAT[C/G]AAGGCTTCTGTCTTT | 899 |
rs9937793 | snp | A/G | 0.117886 | 0.21224 | intron-variant | CCNF | GRCh38.p7 | 16:2435280 | aagaaaagaaaaaaa[A/G]AAAGAAATGTTCTAG | 899 |
rs11248924 | snp | C/T | 0.0314385 | 0.121371 | intron-variant | CCNF | GRCh38.p7 | 16:2439969 | GGGACACCCTAAGAT[C/T]GGTTCAGCACTGGAA | 899 |
rs11552572 | snp | C/T | 0.00478085 | 0.0486577 | utr-variant-3-prime, intron-variant | CCNF, LOC105371050 | GRCh38.p7 | 16:2457521 | TCGGCCTGCATGGGG[C/T]ACCCACTTCCTTCTG | 899 |
rs11639797 | snp | C/T | 0.311614 | 0.242289 | intron-variant | CCNF | GRCh38.p7 | 16:2441264 | agctggatgtggtgg[C/T]gtgtgccttgtagtg | 899 |
rs11639853 | snp | G/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2449033 | CGCTGTGCTGGAGGG[G/T]GGGGGTGGGCATTCA | 899 |
rs11642437 | snp | C/T | 0.316726 | 0.240931 | intron-variant | CCNF | GRCh38.p7 | 16:2448336 | GTCTGCCTAACAGCC[C/T]TGCTGCTTTCTGTCT | 899 |
rs11643319 | snp | A/G | 0.312104 | 0.242163 | intron-variant | CCNF | GRCh38.p7 | 16:2441244 | tctcaaaaaaaaaaa[A/G]aattagctggatgtg | 899 |
rs11643323 | snp | C/G | 0.311614 | 0.242289 | intron-variant | CCNF | GRCh38.p7 | 16:2441322 | gatcacttgagcctg[C/G]gaggtcaaagctgca | 899 |
rs11643674 | snp | C/G | 0.312348 | 0.242101 | intron-variant | CCNF | GRCh38.p7 | 16:2442082 | acaatctcggctcac[C/G]acaagctccgcctcc | 899 |
rs11643922 | snp | C/T | 0.312348 | 0.242101 | intron-variant | CCNF | GRCh38.p7 | 16:2442028 | ttgttttgttttTga[C/T]ggagtcttgctctgt | 899 |
rs11644790 | snp | A/G | 0.312348 | 0.242101 | intron-variant | CCNF | GRCh38.p7 | 16:2442359 | tttataatatctatt[A/G]ttatattataacata | 899 |
rs11647333 | snp | C/T | 0.316243 | 0.241064 | intron-variant, downstream-variant-500B | CCNF | GRCh38.p7 | 16:2447364 | CTGATGTGGGCGGAT[C/T]GTGAGGTCAGGAGTT | 899 |
rs11647929 | snp | C/G | 0.359364 | 0.22481 | intron-variant, upstream-variant-2KB | CCNF, MIR6767 | GRCh38.p7 | 16:2444474 | ccagctaattttttt[C/G]tatttttagtagaga | 899 |
rs11648521 | snp | C/T | 0.316243 | 0.241064 | intron-variant, downstream-variant-500B | CCNF | GRCh38.p7 | 16:2447682 | CTTGAACCTGGGAGG[C/T]GGAGGTTGCAGTGAG | 899 |
rs11648784 | snp | G/T | 0.316243 | 0.241064 | intron-variant | CCNF | GRCh38.p7 | 16:2448203 | TCACCCACCTTCTGG[G/T]TCTATAACATTTCTA | 899 |
rs12596168 | snp | A/T | 0.0142736 | 0.0832652 | intron-variant | CCNF | GRCh38.p7 | 16:2442466 | atataattataatat[A/T]ataatataatatatA | 899 |
rs12598626 | snp | A/C | 0 | 0 | intron-variant | CCNF | GRCh38.p7 | 16:2452079 | TTTCCTCGTGCGCTC[A/C]CAGCTTGGGGACTGG | 899 |
rs12919256 | snp | A/G | 0.316243 | 0.241064 | intron-variant | CCNF | GRCh38.p7 | 16:2450380 | gctgggcgtggtggc[A/G]tgcgcctgcaatccc | 899 |
rs12919823 | snp | A/C | | | intron-variant | CCNF | GRCh38.p7 | 16:2442840 | atgtaatattatatt[A/C]tattatatataatat | 899 |
rs12919892 | snp | C/G | 0.316243 | 0.241064 | intron-variant | CCNF | GRCh38.p7 | 16:2450070 | AAATTAGCCAGGCGT[C/G]GTGGTGCACGCCTAT | 899 |
rs12920281 | snp | A/G | | | upstream-variant-2KB, intron-variant | CCNF | GRCh38.p7 | 16:2429077 | GTCGCCGGGGTCAGC[A/G]GCGAAGCCCGAACCC | 899 |
rs12921396 | snp | A/T | 0.312593 | 0.242037 | intron-variant | CCNF | GRCh38.p7 | 16:2436997 | ATCCTGGAGGGCTCT[A/T]CTCTCCTGAAACACA | 899 |
rs12922325 | snp | A/G | 0.304438 | 0.244001 | intron-variant | CCNF | GRCh38.p7 | 16:2456022 | AAAAATTAGCTGGGC[A/G]TCGTGGCGTGCGCCT | 899 |
rs12923030 | snp | A/G | 0.165527 | 0.235296 | intron-variant | CCNF | GRCh38.p7 | 16:2430947 | TCTGTAATTTGTGCA[A/G]TGCCACTCCTTTACA | 899 |
rs12923576 | snp | C/G | 0.255782 | 0.249933 | intron-variant | CCNF | GRCh38.p7 | 16:2456129 | TCATGCCACTGCACT[C/G]TAGCCTGGGCGTTCT | 899 |
rs12924201 | snp | G/T | | | upstream-variant-2KB, intron-variant | CCNF | GRCh38.p7 | 16:2429204 | GGGTTCCACCAATCA[G/T]CGGCCAATGTTCGAA | 899 |
rs12924238 | snp | G/T | | | upstream-variant-2KB, intron-variant | CCNF | GRCh38.p7 | 16:2429277 | GGGAGGGCGTGGAGG[G/T]CGGTAAATGAGGCGA | 899 |
rs12924302 | snp | A/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2442834 | taatatatgtaatat[A/T]atattctattatata | 899 |
rs12924306 | snp | A/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2442844 | aatattatattctat[A/T]atatataatatatat | 899 |
rs12924374 | snp | G/T | | | upstream-variant-2KB, intron-variant | CCNF | GRCh38.p7 | 16:2429311 | CAGGGCGGGACATgg[G/T]cggggccggcggcgg | 899 |
rs12924383 | snp | G/T | | | upstream-variant-2KB, intron-variant | CCNF | GRCh38.p7 | 16:2429323 | Tgggcggggccggcg[G/T]cggcccccccgggcA | 899 |
rs12924403 | snp | C/G | | | upstream-variant-2KB, intron-variant | CCNF | GRCh38.p7 | 16:2429365 | GGGCCGGGTGCGTTT[C/G]AAAACTGGGGTGGGC | 899 |
rs12924405 | snp | A/G | | | upstream-variant-2KB, intron-variant | CCNF | GRCh38.p7 | 16:2429375 | CGTTTGAAAACTGGG[A/G]TGGGCGGCGGGGCGG | 899 |
rs12924408 | snp | A/G | | | upstream-variant-2KB, intron-variant | CCNF | GRCh38.p7 | 16:2429382 | AAACTGGGGTGGGCG[A/G]CGGGGCGGGGTCTGC | 899 |
rs12925160 | snp | C/G/T | | | upstream-variant-2KB, intron-variant | CCNF | GRCh38.p7 | 16:2429150 | CGGGAAGCGCTCCTA[C/G/T]GGGACCCCAGCCCCG | 899 |
rs12925730 | snp | C/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2431403 | TGGGGCAGAggccag[C/G]cacggtggctcatgc | 899 |
rs12926008 | snp | C/T | 0.312593 | 0.242037 | intron-variant | CCNF | GRCh38.p7 | 16:2438210 | AGCAGCAGAAGGGGG[C/T]GTCCAAGGCCCAAAA | 899 |
rs12926827 | snp | C/T | 0.311369 | 0.242351 | intron-variant | CCNF | GRCh38.p7 | 16:2438692 | TGGTGAGTAGAGTGA[C/T]TGAACATCAAGTAAA | 899 |
rs12926965 | snp | A/T | 0.316 | 0.241131 | intron-variant, utr-variant-3-prime | CCNF | GRCh38.p7 | 16:2446965 | CATTCCCATGGAAGG[A/T]GGGAGCAAACCCTGC | 899 |
rs12926991 | snp | C/T | 0.316243 | 0.241064 | intron-variant, utr-variant-3-prime | CCNF | GRCh38.p7 | 16:2447009 | AGCTGTCTTCAGATG[C/T]GCTCTTGGGCCTGAA | 899 |
rs12927391 | snp | A/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2431401 | GTTGGGGCAGAggcc[A/G]ggcacggtggctcat | 899 |
rs12928724 | snp | G/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2434549 | ccaggaggcagaggt[G/T]gcagtgagccgagat | 899 |
rs12928789 | snp | A/G | 0.398987 | 0.200768 | intron-variant | CCNF | GRCh38.p7 | 16:2435895 | CCTCACCCCACCTGC[A/G]TGTTGGCGCTTCAGA | 899 |
rs12932220 | snp | C/G | 0.362313 | 0.223351 | intron-variant | CCNF | GRCh38.p7 | 16:2450603 | TCATTGCACAGGCAG[C/G]AGAACATACTAGAAA | 899 |
rs12932533 | snp | C/G | 0.316 | 0.241131 | intron-variant | CCNF | GRCh38.p7 | 16:2450824 | TCATAGTGCAGCGGA[C/G]ACCACGTGGCCCCCA | 899 |
rs12932646 | snp | A/G | 0.328148 | 0.237472 | intron-variant | CCNF | GRCh38.p7 | 16:2450843 | ACGTGGCCCCCAGTC[A/G]GGAAAATACTCCCCT | 899 |
rs12932700 | snp | A/G | 0.311369 | 0.242351 | intron-variant | CCNF | GRCh38.p7 | 16:2436181 | CCTGCCCTGTGCGCC[A/G]TGAGCACGCAGACCT | 899 |
rs12933696 | snp | A/G | 0.316243 | 0.241064 | intron-variant | CCNF | GRCh38.p7 | 16:2450446 | aacccgggaggcaga[A/G]gttgcggtgagccga | 899 |
rs12933758 | snp | C/T | 0.305436 | 0.243776 | intron-variant | CCNF | GRCh38.p7 | 16:2435576 | GGCAACAGAGCAAGA[C/T]CCTGTCTCAGAGAGA | 899 |
rs12933884 | snp | C/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2435646 | gcacacacacacaca[C/T]atatatatgcacaca | 899 |
rs12933887 | snp | C/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2435648 | acacacacacacata[C/T]atatatgcacacaca | 899 |
rs12933944 | snp | A/C | | | intron-variant | CCNF | GRCh38.p7 | 16:2441872 | AAATTGGAATGTTCA[A/C]CCTTACTACTAGTCA | 899 |
rs13329909 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | CCNF | GRCh38.p7 | 16:2433844 | GGCGGGCATTTTTCT[C/G]ACAGGGATTCGCTGT | 899 |
rs13331211 | snp | C/G | 0.0729998 | 0.176553 | intron-variant | CCNF | GRCh38.p7 | 16:2434546 | aacccaggaggcaga[C/G]gttgcagtgagccga | 899 |
rs13331598 | snp | C/G | 0.166616 | 0.235684 | utr-variant-5-prime, intron-variant | CCNF | GRCh38.p7 | 16:2429481 | CGACGCGAGCGCGGC[C/G]ATGGGGAGCGGCGGC | 899 |
rs13334470 | snp | A/G | 0.191775 | 0.243125 | intron-variant | CCNF | GRCh38.p7 | 16:2454826 | GCACTTTGGGAGGCC[A/G]AGGTGGGCGGATCAC | 899 |
rs13334755 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | CCNF | GRCh38.p7 | 16:2454824 | cagcactttgggagg[C/T]cgaggtgggcggatc | 899 |
rs13337091 | snp | A/C | 0.308661 | 0.24302 | intron-variant | CCNF | GRCh38.p7 | 16:2429711 | GCCCGAGCCCCTCGG[A/C]GCCTTCCCCCGCGGC | 899 |
rs28417759 | snp | A/G | 0.401428 | 0.198921 | intron-variant | CCNF | GRCh38.p7 | 16:2448827 | CAGGAAGTGGGCTCC[A/G]CCCTGAGACCCCTTC | 899 |
rs28483668 | snp | A/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2443169 | ATATATTATATATAA[A/T]ATATATATAATATAT | 899 |
rs28509233 | snp | A/G | 0.0456336 | 0.143994 | intron-variant | CCNF | GRCh38.p7 | 16:2456305 | GTTGCTTGCTTCTGC[A/G]TCCACTTGGCTTGAG | 899 |
rs28534068 | snp | A/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2442752 | TAATTATATAATAAT[A/T]ATAATAATATAATAT | 899 |
rs28550541 | snp | G/T | 0.36315 | 0.222928 | intron-variant | CCNF | GRCh38.p7 | 16:2437419 | ACCCTGGAAAGTCAG[G/T]AGCCTAAGGGAAGTG | 899 |
rs28562606 | snp | A/G | 0.0322114 | 0.122752 | intron-variant | CCNF | GRCh38.p7 | 16:2435458 | AGCATGGTGGCACAT[A/G]CCTGTAGTCCTAGCT | 899 |
rs28581299 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | CCNF | GRCh38.p7 | 16:2438859 | AAAAATTAGCCGGGC[A/G]TGGTGGTGGGCACCT | 899 |
rs28616628 | snp | A/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2443178 | ATATAATATATATAT[A/T]ATATATAATATATAT | 899 |
rs28625380 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant, utr-variant-3-prime | CCNF | GRCh38.p7 | 16:2446759 | ATGTTTTTTGTTTCA[C/T]GAGGAAGCAGAGGAG | 899 |
rs28628258 | snp | G/T | 0.0166325 | 0.0896639 | intron-variant, utr-variant-3-prime | CCNF | GRCh38.p7 | 16:2446723 | ACCCAGAGGCAGAGG[G/T]TCCAGGCTCAGGTCA | 899 |
rs28642228 | snp | A/C | 0.0146672 | 0.084371 | intron-variant | CCNF | GRCh38.p7 | 16:2454121 | AGCACCATGTGCACC[A/C]GTAACCTTCCCAAGG | 899 |
rs28647184 | snp | G/T | 0.312104 | 0.242163 | intron-variant | CCNF | GRCh38.p7 | 16:2439532 | TGGTCCTTGGATGCG[G/T]TTCTGTCCACAAAAG | 899 |
rs28663296 | snp | G/T | 0.312104 | 0.242163 | intron-variant, downstream-variant-500B | CCNF, MIR6767 | GRCh38.p7 | 16:2445729 | GTTTTGTTTTGTGTT[G/T]TTTTTTTTTTTTTCC | 899 |
rs28666998 | snp | A/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2443176 | ATATATAATATATAT[A/G]TAATATATAATATAT | 899 |
rs28670436 | snp | A/G | 0.412807 | 0.189721 | intron-variant | CCNF | GRCh38.p7 | 16:2448848 | AGACCCCTTCTCGGC[A/G]TTGCAGGTTTATCAG | 899 |
rs28700212 | snp | A/G | 0 | 0 | intron-variant | CCNF | GRCh38.p7 | 16:2442975 | TTTATATATTTATAT[A/G]TTATATATTATTTAT | 899 |
rs28754702 | snp | C/T | 0.0482946 | 0.147699 | intron-variant | CCNF | GRCh38.p7 | 16:2451673 | CTTTTGTGTCAGCCT[C/T]CCGAGTAGCAGAAAC | 899 |
rs28758190 | snp | C/T | 0.311369 | 0.242351 | intron-variant | CCNF | GRCh38.p7 | 16:2437483 | AACGCATCTGGAAAT[C/T]AGCTGGCACAGAGGA | 899 |
rs34068510 | in-del | -/A | | | intron-variant | CCNF | GRCh38.p7 | 16:2437922 | AAAAAAAAAAAAAAA[-/A]GACTGAAATCTGGGA | 899 |
rs34141593 | in-del | -/A | | | intron-variant | CCNF | GRCh38.p7 | 16:2456011 | CAAAAAATTTAAAAA[-/A]TTAGCTGGGCATCGT | 899 |
rs34183952 | in-del | -/G | | | intron-variant, downstream-variant-500B | CCNF | GRCh38.p7 | 16:2447778 | AGATTTTAAAGGCTG[-/G]AGCTGCCCCCCACCT | 899 |
rs34262718 | in-del | -/C | | | intron-variant | CCNF | GRCh38.p7 | 16:2455840 | CGTGTTGGGAGGACC[-/C]TCACTAGGATGAGGG | 899 |
rs34319199 | in-del | -/A | | | intron-variant | CCNF | GRCh38.p7 | 16:2456152 | GCGTTCTTTCTAGAA[-/A]TGTTGTTTGAGGTGT | 899 |
rs34401552 | in-del | -/C | 0.31014 | 0.242659 | upstream-variant-2KB, intron-variant | CCNF | GRCh38.p7 | 16:2428745 | CCGCGGGGGAGACTT[-/C]CCAGCGTCAGCTCCG | 899 |
rs34430433 | in-del | -/TT | | | intron-variant, downstream-variant-500B | CCNF, MIR6767 | GRCh38.p7 | 16:2445742 | TGTTTTTTTTTTTTT[-/TT]CCCGAGACCAAGTCT | 899 |
rs34456414 | in-del | -/T | 0.484841 | 0.0857308 | intron-variant | CCNF | GRCh38.p7 | 16:2437011 | ACTCTCCTGAAACAC[-/T]AGCTGCTTTGCACTA | 899 |
rs34792935 | in-del | -/C | | | upstream-variant-2KB, intron-variant | CCNF | GRCh38.p7 | 16:2427818 | GAAATTTGCCTGTCC[-/C]ATGTTGAAAGGAGAG | 899 |
rs34899969 | in-del | -/A | | | intron-variant | CCNF | GRCh38.p7 | 16:2440720 | ATGCTAGGGACAAAA[-/A]TTACAAATTGATAAT | 899 |
rs34956143 | in-del | -/T | 0.31721 | 0.240796 | intron-variant | CCNF | GRCh38.p7 | 16:2435424 | CTAGAAAAGAAAATA[-/T]TTTTTTTTTGACTAG | 899 |
rs35053021 | in-del | -/AT | 0.5 | 0 | intron-variant | CCNF | GRCh38.p7 | 16:2437855 | ATGAGCCGTGACTAT[-/AT]GCCAATGCACTCCAG | 899 |
rs35090353 | in-del | -/T | 0.329084 | 0.237162 | intron-variant, upstream-variant-2KB | CCNF, MIR6767 | GRCh38.p7 | 16:2444901 | AACACATTGAACATC[-/T]TTTTTTTTTTTTTGA | 899 |
rs35214798 | snp | A/T | 0.000165098 | 0.00908415 | missense, downstream-variant-500B | CCNF, MIR6767 | GRCh38.p7 | 16:2445550 | AGCCTCCTCCGCAGG[A/T]ACCGGTCCACACACT | 899 |
rs35258963 | in-del | -/T | | | intron-variant, upstream-variant-2KB | CCNF, MIR6767 | GRCh38.p7 | 16:2443925 | CCTTTTTTTTTTTTT[-/T]GAAGTGGAGTCTCGC | 899 |
rs35354034 | in-del | -/T | | | intron-variant, utr-variant-3-prime | CCNF | GRCh38.p7 | 16:2446960 | GTGTCATTCCCATGG[-/T]AAGGAGGGAGCAAAC | 899 |
rs35354174 | in-del | -/G | | | utr-variant-3-prime, upstream-variant-2KB, intron-variant | CCNF, C16orf59, LOC105371050 | GRCh38.p7 | 16:2458503 | ATCCGCCCACTTCGG[-/G]TCTCCCAAAGTGCTG | 899 |
rs35654985 | in-del | -/CT | 0.313814 | 0.241719 | intron-variant, upstream-variant-2KB | CCNF, MIR6767 | GRCh38.p7 | 16:2444983 | TGTAACCTCTGCCTC[-/CT]GGGCTCAAGCCTTTC | 899 |
rs35757483 | in-del | -/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2433438 | CGTTTCACTCACTGG[-/G]CTGATCCCACCCCAA | 899 |
rs35774042 | in-del | -/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2437012 | CTCTCCTGAAACACA[-/T]GCTGCTTTGCACTAT | 899 |
rs36008785 | snp | A/C | 0.00174644 | 0.0294986 | missense | CCNF | GRCh38.p7 | 16:2448948 | CAAGGCGGAGACGAT[A/C]TCGCCCATCATTCTC | 899 |
rs55737759 | in-del | -/ATATATATATATATATAT | | | intron-variant | CCNF | GRCh38.p7 | 16:2441965 | TATATATATATATAT[-/ATATATATATATATATAT]GTTTTTGTTTTTGTT | 899 |
rs56025006 | in-del | -/A | | | intron-variant | CCNF | GRCh38.p7 | 16:2450510 | GTGAAACTCCATCTC[-/A]AAAAAAAAAAAAAAA | 899 |
rs56677463 | snp | A/G | 0.497736 | 0.0335688 | intron-variant | CCNF | GRCh38.p7 | 16:2449785 | CCCTCCATCCCCTCC[A/G]TCCCCTCCATCCCCT | 899 |
rs56708126 | snp | C/G | 0.0872718 | 0.189788 | intron-variant, upstream-variant-2KB | CCNF, MIR6767 | GRCh38.p7 | 16:2444201 | TGGGATTACAGGCGT[C/G]AGCCACCGCGCCCAG | 899 |
rs56716750 | in-del | -/CATATATATGCACACACA | | | intron-variant | CCNF | GRCh38.p7 | 16:2435628 | GCACACACACACACA[-/CATATATATGCACACACA]TATATATATGCACAC | 899 |
rs57863682 | snp | A/C/T | 0.14455 | 0.22847 | intron-variant | CCNF | GRCh38.p7 | 16:2442469 | ATAATATAATATTAT[A/C/T]ATATATAATATATAA | 899 |
rs57972250 | in-del | -/AT | 0.314544 | 0.241524 | intron-variant | CCNF | GRCh38.p7 | 16:2435597 | CTCAGAGAGAGAGAG[-/AT]ATATATATATATATG | 899 |
rs58394198 | in-del | -/AT | | | intron-variant | CCNF | GRCh38.p7 | 16:2441982 | TATATATATATATAT[-/AT]GTTTTTGTTTTTGTT | 899 |
rs58466261 | in-del | -/TAT | | | intron-variant | CCNF | GRCh38.p7 | 16:2442616 | ATAATATAATATTAT[-/TAT]ATATAATATATAATA | 899 |
rs58471778 | snp | C/G | 0.410061 | 0.192043 | intron-variant | CCNF | GRCh38.p7 | 16:2430428 | CTGAGAAGCATGTCC[C/G]GGCTGCCTGCCTGGT | 899 |
rs58763550 | in-del | -/A | | | intron-variant | CCNF | GRCh38.p7 | 16:2442435 | TATAATATTATTATA[-/A]TATAATATATAATAT | 899 |
rs58800938 | snp | A/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2442494 | ATATAATATTATATA[A/T]TATAATATTATTATA | 899 |
rs59027174 | snp | A/G | 0.313326 | 0.241847 | intron-variant | CCNF | GRCh38.p7 | 16:2443158 | TTGTATATAATATAT[A/G]TTATATATAATATAT | 899 |
rs59129256 | snp | C/T | 0.35809 | 0.225425 | upstream-variant-2KB, intron-variant | CCNF | GRCh38.p7 | 16:2429060 | TGGCACCGCAGATGC[C/T]GGTCGCCGGGGTCAG | 899 |
rs59606108 | snp | A/C | | | intron-variant | CCNF | GRCh38.p7 | 16:2452221 | ACTCCCTGGGGGTCT[A/C]GATGCCCTTGAGCAG | 899 |
rs60029686 | snp | A/C | 0.029116 | 0.117091 | intron-variant | CCNF | GRCh38.p7 | 16:2440592 | AGAGCAAGACTCTGT[A/C]TGAAGGAAAAAAAAA | 899 |
rs60354639 | in-del | -/TAT | | | intron-variant | CCNF | GRCh38.p7 | 16:2442543 | ATAATATAATATTAT[-/TAT]ATATAATATATAATA | 899 |
rs60998614 | snp | C/G | | | missense | CCNF | GRCh38.p7 | 16:2455399 | CCACCTTGCAGGAAG[C/G]GGGAGAACAGCCTCC | 899 |
rs61432051 | snp | A/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2442439 | AATATTATTATATAT[A/T]ATATATAATATTATA | 899 |
rs61568968 | in-del | -/CACATATATATA | | | intron-variant | CCNF | GRCh38.p7 | 16:2435664 | ATATATGCACACACA[-/CACATATATATA]TATATATATATATAT | 899 |
rs61728452 | in-del | -/ATATATAATATATATATA | | | intron-variant | CCNF | GRCh38.p7 | 16:2443179 | TATAATATATATATA[-/ATATATAATATATATATA]TTTCTCTGTTTTTGG | 899 |
rs61755288 | snp | A/G | 0.0197763 | 0.0974528 | missense, downstream-variant-500B | CCNF, LOC105371050 | GRCh38.p7 | 16:2456799 | AGTCCCACAAGCTCC[A/G]TGGACGGTGGCTTGG | 899 |
rs62040704 | snp | A/G | 0.0667028 | 0.170006 | intron-variant | CCNF | GRCh38.p7 | 16:2430079 | AATCTTTGAGAATTC[A/G]TCGCCCTGGAATACG | 899 |
rs71148135 | in-del | -/ATATATATAT | 0 | 0 | intron-variant | CCNF | GRCh38.p7 | 16:2435704 | TGTTCCCTGAATTGA[-/ATATATATAT]ATATATATATATATA | 899 |
rs71386672 | snp | A/C | 0.00874735 | 0.0655527 | intron-variant, upstream-variant-2KB | CCNF, MIR6767 | GRCh38.p7 | 16:2444180 | CGCTTTGGCCTCCCA[A/C]AGTGCTGGGATTACA | 899 |
rs71386673 | snp | A/G | 0.5 | 0 | intron-variant | CCNF | GRCh38.p7 | 16:2454584 | AGGCCCTGGGGTCAG[A/G]AAGTGGAAAGGCTCA | 899 |
rs71386674 | snp | A/G | 0.5 | 0 | intron-variant, downstream-variant-500B, upstream-variant-2KB | CCNF, C16orf59, LOC105371050 | GRCh38.p7 | 16:2459343 | CACCAACTACATGGG[A/G]CCCTGCTGCCTTCCT | 899 |
rs71394738 | in-del | -/A | 0.5 | 0 | intron-variant | CCNF | GRCh38.p7 | 16:2435702 | TATATATATATATAT[-/A]TATATATATATTCAA | 899 |
rs71394739 | in-del | -/T | 0.5 | 0 | intron-variant | CCNF | GRCh38.p7 | 16:2435705 | TATATATATATATAT[-/T]CAATTCAGGGAACAA | 899 |
rs72526700 | in-del | -/CC/CT | | | intron-variant, upstream-variant-2KB | CCNF, MIR6767 | GRCh38.p7 | 16:2444982 | CTGTAACCTCTGCCT[-/CC/CT]CGGGCTCAAGCCTTT | 899 |
rs72768719 | snp | C/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2452303 | CAGGGGACCTGGTGG[C/T]ATCTCCCGGGCTTTG | 899 |
rs73488284 | snp | C/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2434680 | GTATACTGAGAGTTG[C/T]ACAGACATCACCAGT | 899 |
rs73490247 | snp | A/G | 0.02016 | 0.0983543 | utr-variant-3-prime, intron-variant | CCNF, LOC105371050 | GRCh38.p7 | 16:2457462 | GTTTGGGGCTTCAGT[A/G]GGGAGCTGACAGCTG | 899 |
rs74003003 | snp | A/G | 0.0356815 | 0.128715 | intron-variant, downstream-variant-500B | CCNF, LOC105371050 | GRCh38.p7 | 16:2456412 | CCCACGCTTCTCACC[A/G]CAGGAGGGTAACACA | 899 |
rs74006624 | snp | A/C/T | 0.0314385 | 0.121371 | intron-variant | CCNF | GRCh38.p7 | 16:2446573 | CCTAAACCAGCTGTC[A/C/T]CCAGCATGGTCTACA | 899 |
rs74006627 | snp | A/G | 0.0314385 | 0.121371 | intron-variant | CCNF | GRCh38.p7 | 16:2452777 | TTCTGTACATTCCAT[A/G]TAAATGGCGTCATCG | 899 |
rs74622580 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | CCNF | GRCh38.p7 | 16:2455261 | AGCTTCACCGGCATC[A/T]TCTTCGTAGCAGAAC | 899 |
rs75100731 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | CCNF | GRCh38.p7 | 16:2430473 | TCTCACCTTTAATGA[C/T]TGCATCTGTACACAA | 899 |
rs75101417 | snp | C/G | 0.00993419 | 0.0697739 | intron-variant | CCNF | GRCh38.p7 | 16:2435718 | ATTCAATTCAGGGAA[C/G]AAGTATTCTGACTTC | 899 |
rs75167067 | snp | C/G | 0.5 | 0 | intron-variant | CCNF | GRCh38.p7 | 16:2434396 | AAGGCGGGCGGATCA[C/G]GAGGTCAAGAGTTTG | 899 |
rs75177396 | snp | A/G | 0.0581099 | 0.160244 | intron-variant | CCNF | GRCh38.p7 | 16:2430442 | CGGGCTGCCTGCCTG[A/G]TGGGTGGAATGCCCG | 899 |
rs75680089 | in-del | -/CTTT | | | utr-variant-3-prime, upstream-variant-2KB, intron-variant | CCNF, C16orf59, LOC105371050 | GRCh38.p7 | 16:2458253 | AGTGTCCCCCAGATG[-/CTTT]TTTTTTTTTTTTTTT | 899 |
rs75733444 | snp | C/T | 0.309894 | 0.242719 | intron-variant | CCNF | GRCh38.p7 | 16:2435628 | GCACACACACACACA[C/T]ATATATATGCACACA | 899 |
rs76161396 | snp | C/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2434818 | ATTTTCTGTCTCTCC[C/G]GATTTGCCTTTTGTG | 899 |
rs76327579 | snp | C/G | 0.0256215 | 0.110247 | utr-variant-3-prime, intron-variant | CCNF, LOC105371050 | GRCh38.p7 | 16:2457897 | CAAAAAGAATTTTCC[C/G]AGATAGGCTAGCCAG | 899 |
rs76363370 | snp | G/T | 0 | 0 | intron-variant, upstream-variant-2KB | CCNF, MIR6767 | GRCh38.p7 | 16:2444318 | TTTTTTTTTTTTTTT[G/T]AGACGGAGTCTTGCT | 899 |
rs76453499 | snp | C/T | 0.040671 | 0.13668 | intron-variant | CCNF | GRCh38.p7 | 16:2432148 | AGTACCCTTTTATGG[C/T]AGTGAAATTTGCATC | 899 |
rs76549515 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | CCNF | GRCh38.p7 | 16:2431426 | GCTCATGCCTTAATC[C/G]TAGCACTTTGGGAGG | 899 |
rs76888533 | snp | C/T | | | intron-variant, upstream-variant-2KB | CCNF, MIR6767 | GRCh38.p7 | 16:2444078 | GCACCCACCACCATG[C/T]CCGGCTAATTTTTTG | 899 |
rs77093646 | snp | A/C | 0.5 | 0 | intron-variant | CCNF | GRCh38.p7 | 16:2455083 | AAAAAAAAAAAAAAA[A/C]ACTGGAAGGTGGCAT | 899 |
rs77375192 | snp | A/C | 0.057006 | 0.159019 | intron-variant | CCNF | GRCh38.p7 | 16:2452268 | TCTGCTTTTTCTCCC[A/C]CCATGCTGTGCTCCA | 899 |
rs77490966 | snp | C/T | 0.0244538 | 0.107838 | intron-variant | CCNF | GRCh38.p7 | 16:2452265 | CCATCTGCTTTTTCT[C/T]CCACCATGCTGTGCT | 899 |
rs77508260 | snp | C/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2434819 | TTTTCTGTCTCTCCG[C/G]ATTTGCCTTTTGTGA | 899 |
rs77576598 | snp | G/T | 0 | 0 | intron-variant, upstream-variant-2KB | CCNF, MIR6767 | GRCh38.p7 | 16:2443937 | CCCTTTTTTTTTTTT[G/T]GAAGTGGAGTCTCGC | 899 |
rs77641229 | snp | G/T | 0 | 0 | intron-variant, upstream-variant-2KB | CCNF, MIR6767 | GRCh38.p7 | 16:2444317 | TTTTTTTTTTTTTTT[G/T]GAGACGGAGTCTTGC | 899 |
rs78443348 | snp | A/G | 0.0433465 | 0.140692 | upstream-variant-2KB, intron-variant | CCNF | GRCh38.p7 | 16:2428877 | GGCCGTGCAAGCTGG[A/G]GGTGAGGGTCGCGGG | 899 |
rs78604417 | snp | C/T | 0.5 | 0 | intron-variant, utr-variant-3-prime | CCNF | GRCh38.p7 | 16:2447276 | CTCTGCCTTATTATC[C/T]TTTTTTTTTTTTTTT | 899 |
rs78649157 | snp | A/C/G/T | 0.00159617 | 0.0282053 | intron-variant | CCNF | GRCh38.p7 | 16:2439910 | TGGGCTCCCACATTG[A/C/G/T]GGGGCAGGACTATCT | 899 |
rs78667058 | snp | C/T | 0.5 | 0 | intron-variant, utr-variant-3-prime | CCNF | GRCh38.p7 | 16:2447275 | ACTCTGCCTTATTAT[C/T]TTTTTTTTTTTTTTT | 899 |
rs78671515 | snp | A/G | 0.0225045 | 0.103662 | intron-variant, upstream-variant-2KB | CCNF, MIR6767 | GRCh38.p7 | 16:2445288 | GCTGGGACCCACGGA[A/G]CCTCCCGGGCTTCCT | 899 |
rs79038845 | snp | C/T | 0.0228947 | 0.104514 | upstream-variant-2KB, intron-variant | CCNF | GRCh38.p7 | 16:2429212 | CCAATCAGCGGCCAA[C/T]GTTCGAATTCGCGTC | 899 |
rs79484787 | snp | A/G | | | upstream-variant-2KB, intron-variant | CCNF | GRCh38.p7 | 16:2428296 | AGCCTGCACGCCAGG[A/G]CTCCTGTCTGTGTGC | 899 |
rs79593033 | snp | C/G | 0.0174175 | 0.0916809 | intron-variant | CCNF | GRCh38.p7 | 16:2430176 | AATCGCTAGGAAGTC[C/G]TAGCAAGGCGGGGAG | 899 |
rs79713355 | snp | A/G | 0.00313082 | 0.0394412 | intron-variant | CCNF | GRCh38.p7 | 16:2453585 | AATGCTGGCATCCTC[A/G]TGCCGGCCCAGTTCC | 899 |
rs79965049 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | CCNF, LOC105371050 | GRCh38.p7 | 16:2457290 | GGCACCTCTCTGTCC[C/T]TTCCGTGTCTCACTG | 899 |
rs79971552 | snp | A/C/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2435143 | GTGGTCCCAGCTACT[A/C/T]GGGAGGCTGAGGCAG | 899 |
rs80103765 | snp | A/C | 0.5 | 0 | intron-variant | CCNF | GRCh38.p7 | 16:2441234 | CGATACTCCATCTCA[A/C]AAAAAAAAAAAATTA | 899 |
rs80106090 | snp | A/T | 0.0283406 | 0.115616 | intron-variant | CCNF | GRCh38.p7 | 16:2452672 | CCAAAGGGACAACAC[A/T]CCCCTCAGCTGTCAC | 899 |
rs80281995 | snp | C/G | 0 | 0 | intron-variant | CCNF | GRCh38.p7 | 16:2452204 | TCCAGGATGAGATCA[C/G]AACTCCCTGGGGGTC | 899 |
rs80290294 | snp | A/G | | | utr-variant-3-prime, upstream-variant-2KB, downstream-variant-500B, nc-transcript-variant | CCNF, C16orf59, LOC105371050 | GRCh38.p7 | 16:2458851 | TGTGAGGAGGATAGT[A/G]GCAGATGAGTGATGG | 899 |
rs80306735 | snp | C/T | | | intron-variant, upstream-variant-2KB | CCNF, MIR6767 | GRCh38.p7 | 16:2444557 | CGCCTGCCTCCGCCT[C/T]CCAAAGTGCTGGGAT | 899 |
rs111218516 | snp | C/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2442910 | ATATTATATAATATA[C/T]AAATATATATTAATA | 899 |
rs111218519 | snp | C/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2442653 | AATATAATATTATTA[C/T]ATATAATATATAATA | 899 |
rs111218534 | snp | A/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2442809 | ATTCTATAATATATA[A/T]TATATTCTATAATAT | 899 |
rs111348985 | snp | A/C/G | 0.00199481 | 0.0315187 | intron-variant | CCNF | GRCh38.p7 | 16:2449572 | CCTGGTTACTTCTTG[A/C/G]GGGGTGAGATACAGC | 899 |
rs111364812 | snp | A/G | 0.5 | 0 | intron-variant | CCNF | GRCh38.p7 | 16:2451359 | GGCTGGGGGCCATGA[A/G]TGGAGTCATGGCAGT | 899 |
rs111520609 | snp | C/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2435666 | ATATGCACACACACA[C/T]ATATATATATATATA | 899 |
rs111543933 | snp | A/G | 0.000649583 | 0.0180103 | synonymous-codon | CCNF | GRCh38.p7 | 16:2449296 | GGTCCCCACTGTGGT[A/G]GATTACAAGGAGGTC | 899 |
rs111549830 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CCNF | GRCh38.p7 | 16:2430562 | ACTCCGCATTCTACA[A/G]TAGAGGGCACACTGA | 899 |
rs111583860 | snp | A/G | 0.0267878 | 0.112589 | intron-variant, downstream-variant-500B | CCNF | GRCh38.p7 | 16:2447569 | AGCCTGGGCAATGGC[A/G]CAAGACTCTGTCTCA | 899 |
rs111591563 | in-del | -/GA | 0.5 | 0 | intron-variant | CCNF | GRCh38.p7 | 16:2432824 | TTACTTTCACACAGA[-/GA]TTGGGGACCTCAACT | 899 |
rs111602976 | snp | A/G | | | upstream-variant-2KB, intron-variant | CCNF | GRCh38.p7 | 16:2428245 | CCCTGTGCTGTGATC[A/G]CCTGTTTACTCTGTC | 899 |
rs111630863 | snp | A/G | 0.5 | 0 | intron-variant | CCNF | GRCh38.p7 | 16:2431699 | AAAAAAAAAAAAAAA[A/G]GAGGGCAAAAAGGAA | 899 |
rs111632439 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CCNF | GRCh38.p7 | 16:2441623 | ACTGCAACCTCTGAC[A/G]CCTGGGTTCAAGCCT | 899 |
rs111637411 | snp | G/T | 0.0154538 | 0.0865337 | intron-variant | CCNF | GRCh38.p7 | 16:2455156 | CCACAGCTGAGCCGG[G/T]TGGGCTGGGCTTCAC | 899 |
rs111704404 | snp | A/C/T | 0 | 0 | splice-acceptor-variant | CCNF | GRCh38.p7 | 16:2431128 | GTCTTTTTTTCCTTC[A/C/T]GTGGTCCACTGTAGG | 899 |
rs111853417 | in-del | -/A | 0.312348 | 0.242101 | intron-variant | CCNF | GRCh38.p7 | 16:2443098 | ATATATAATAGATAT[-/A]TTTTATATATAATAT | 899 |
rs112038429 | snp | A/G | 0.5 | 0 | intron-variant | CCNF | GRCh38.p7 | 16:2450821 | AGCTCATAGTGCAGC[A/G]GACACCACGTGGCCC | 899 |
rs112050866 | snp | G/T | 0.5 | 0 | intron-variant | CCNF | GRCh38.p7 | 16:2436927 | GGGCATTGATCACAA[G/T]GACCCACCTGTTCTA | 899 |
rs112075806 | snp | A/C | 0.5 | 0 | intron-variant | CCNF | GRCh38.p7 | 16:2449613 | CCTTCAGTGATGTCC[A/C]AGATTTCTGACCATG | 899 |
rs112243581 | snp | G/T | 0.5 | 0 | intron-variant | CCNF | GRCh38.p7 | 16:2452637 | TCACAACAATCAAAT[G/T]GATGACATTTTCACT | 899 |
rs112284643 | snp | C/T | 0.0441095 | 0.141807 | intron-variant | CCNF | GRCh38.p7 | 16:2451608 | CAGGCTGGAGTGCAG[C/T]GGCACCATCCTAGCT | 899 |
rs112285350 | snp | A/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2451621 | AGTGGCACCATCCTA[A/G]CTCACTGCAGCCCTG | 899 |
rs112322351 | in-del | -/AGATAT | 0.5 | 0 | intron-variant | CCNF | GRCh38.p7 | 16:2435595 | GTCTCAGAGAGAGAG[-/AGATAT]ATATATATATATGCA | 899 |
rs112415601 | snp | C/T | 0.077417 | 0.180873 | intron-variant | CCNF | GRCh38.p7 | 16:2451019 | TCCCTCCACCTGCCC[C/T]GGCCCCTCCGCCCTT | 899 |
rs112459938 | in-del | -/T | 0.5 | 0 | intron-variant | CCNF | GRCh38.p7 | 16:2431837 | ACCTTTTTTTTTTTT[-/T]GAGACAGAGTCTCGC | 899 |
rs112506440 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2430647 | CTTCTCTCCAGGGCC[C/G]ACCCTTCTAATTTGG | 899 |
rs112566974 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | CCNF | GRCh38.p7 | 16:2455349 | GGCCTGGCCTCCCAG[C/T]GCCGCCGTCCATGAC | 899 |
rs112608915 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | CCNF | GRCh38.p7 | 16:2440922 | AGTGAGACTCCATCT[C/T]GACAAAAAATTTTAA | 899 |
rs112736040 | snp | A/G | 0.5 | 0 | intron-variant, downstream-variant-500B | CCNF | GRCh38.p7 | 16:2447529 | GCAGAGGTTGCAGTG[A/G]GCCAAGATTACACCA | 899 |
rs112748256 | snp | A/T | 0.5 | 0 | intron-variant | CCNF | GRCh38.p7 | 16:2431735 | GATGATATCATTACC[A/T]GATGCTTTCTTTAAG | 899 |
rs112769291 | snp | C/G/T | 6.61813e-05 | 0.00575207 | missense, downstream-variant-500B | CCNF, LOC105371050 | GRCh38.p7 | 16:2456835 | CTGCCCCAACCTACC[C/G/T]CAGTGCTGTCCCTGG | 899 |
rs112939661 | snp | A/G | 0.000330826 | 0.012857 | intron-variant | CCNF | GRCh38.p7 | 16:2449073 | CTGTGGGAGGGCCTC[A/G]TGGACTCAGAGAGCA | 899 |
rs113037686 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2431448 | TTTGGGAGGCCGAAG[C/G/T]GGGGTGGATCACCTG | 899 |
rs113141391 | snp | A/C | 0.5 | 0 | utr-variant-3-prime, upstream-variant-2KB, intron-variant | CCNF, C16orf59, LOC105371050 | GRCh38.p7 | 16:2458296 | TTTGCTCTTGTCTCC[A/C]CGGCTGGAGTGCAGT | 899 |
rs113200947 | snp | A/G | 0.5 | 0 | intron-variant | CCNF | GRCh38.p7 | 16:2440030 | AGAGCTGGGAAATGC[A/G]TTATTCATCTCTGCC | 899 |
rs113220942 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | CCNF | GRCh38.p7 | 16:2441224 | GGCAACAGAGCGATA[C/T]TCCATCTCAAAAAAA | 899 |
rs113222489 | snp | C/G | 0.5 | 0 | intron-variant | CCNF | GRCh38.p7 | 16:2437475 | ATATGGGGAACGCAT[C/G]TGGAAATCAGCTGGC | 899 |
rs113278292 | snp | C/T | 0.00137242 | 0.0261596 | intron-variant, downstream-variant-500B | CCNF, MIR6767 | GRCh38.p7 | 16:2445670 | CGTGCTGGCCTTTCC[C/T]GGGTTCAGGGTCACC | 899 |
rs113365553 | snp | C/T | 0.5 | 0 | intron-variant | CCNF | GRCh38.p7 | 16:2451816 | GTCTCCCTTCCCACC[C/T]ACCCCAAGGGGCCCC | 899 |
rs113377497 | snp | C/T | 0.0766824 | 0.180169 | intron-variant | CCNF | GRCh38.p7 | 16:2431775 | TTACAGAAATTCCTA[C/T]TGCTGTCTCCTAGCA | 899 |
rs113432361 | in-del | -/AAAAAAAAAAAA | 0 | 0 | intron-variant | CCNF | GRCh38.p7 | 16:2455058 | GAGCAAGAACACCTC[-/AAAAAAAAAAAA]AAAAAAAAAAAAACA | 899 |
rs113434351 | snp | C/T | 0.5 | 0 | intron-variant | CCNF | GRCh38.p7 | 16:2437356 | CAGCACCTGCGAGGC[C/T]ACCTGCAGGGTCCCA | 899 |
rs113528306 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | CCNF | GRCh38.p7 | 16:2455334 | GAGGCAGGTGTGGAG[A/G]GCCTGGCCTCCCAGC | 899 |
rs113578655 | in-del | -/A | 0.5 | 0 | intron-variant, downstream-variant-500B | CCNF | GRCh38.p7 | 16:2447754 | GGGAAACTCTGTCTC[-/A]AAAAAAAAAAGATTT | 899 |
rs113579900 | snp | A/G | 0.5 | 0 | intron-variant | CCNF | GRCh38.p7 | 16:2448028 | GCCTTGCGGGGGGCC[A/G]CTGGAGCAGCGTGTT | 899 |
rs113592037 | snp | C/G | 0.5 | 0 | intron-variant | CCNF | GRCh38.p7 | 16:2453857 | GTCATGCGCGTCCTG[C/G]ACTTCTCTGCTCCAT | 899 |
rs113675906 | snp | C/T | 0.000417578 | 0.0144435 | intron-variant, nc-transcript-variant | CCNF, MIR6767 | GRCh38.p7 | 16:2445398 | AGGTGGGGTTGAAAT[C/T]GCAGACAGGGACACA | 899 |
rs113705886 | snp | C/T | 0.5 | 0 | utr-variant-3-prime, upstream-variant-2KB, intron-variant | CCNF, C16orf59, LOC105371050 | GRCh38.p7 | 16:2458295 | TTTTGCTCTTGTCTC[C/T]CCGGCTGGAGTGCAG | 899 |
rs113742704 | snp | C/T | 0.5 | 0 | intron-variant | CCNF | GRCh38.p7 | 16:2449491 | CTTCCCAGGGATGCC[C/T]GTGTCGGGGAAGGTG | 899 |
rs113819011 | snp | C/T | 0.0524604 | 0.153226 | intron-variant | CCNF | GRCh38.p7 | 16:2453985 | TCTCAGCACCTTGGC[C/T]GTTCCTCCTGGAGTT | 899 |
rs113831092 | snp | A/G | 0.0741063 | 0.177655 | intron-variant | CCNF | GRCh38.p7 | 16:2437792 | TAGTCCCAGCTACTC[A/G]GGAGGCTGCGGTGGG | 899 |
rs114007390 | snp | A/C/T | 0.0225045 | 0.103662 | intron-variant | CCNF | GRCh38.p7 | 16:2439907 | ATCTGGGCTCCCACA[A/C/T]TGGGGGGCAGGACTA | 899 |
rs114102737 | snp | A/G | 0.0341408 | 0.126114 | intron-variant | CCNF | GRCh38.p7 | 16:2450746 | TGGGGTTTTCTTGGC[A/G]GCAGCCACCCTCACT | 899 |
rs114568350 | snp | A/G | 0.0166325 | 0.0896639 | utr-variant-3-prime, intron-variant | CCNF, LOC105371050 | GRCh38.p7 | 16:2457311 | TGTCTCACTGTCTCT[A/G]GAAGCTTCAGCCCAT | 899 |
rs114805858 | snp | C/T | 0.00636936 | 0.0560724 | upstream-variant-2KB, intron-variant | CCNF | GRCh38.p7 | 16:2427467 | CTCTCATTCCTCCCA[C/T]GCCCCTCTCTGCCTC | 899 |
rs115003111 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant, downstream-variant-500B, upstream-variant-2KB | CCNF, C16orf59, LOC105371050 | GRCh38.p7 | 16:2459123 | TGATGGAGGGGCCCA[C/T]CCGGAGCGCTGGGCC | 899 |
rs115100621 | snp | A/G | 0.00515924 | 0.0505272 | synonymous-codon, nc-transcript-variant | CCNF, LOC105371050 | GRCh38.p7 | 16:2456861 | CCTGGACAGTGACTC[A/G]CACACACAGCCCTGC | 899 |
rs115509745 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | CCNF | GRCh38.p7 | 16:2454461 | CCTGTGCTCAGCCTC[A/G]CTGTGTTAAACCCGC | 899 |
rs115883599 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | CCNF | GRCh38.p7 | 16:2451024 | CCACCTGCCCCGGCC[C/T]CTCCGCCCTTCTCTC | 899 |
rs116176597 | snp | A/G | 0.0146401 | 0.0842955 | intron-variant | CCNF | GRCh38.p7 | 16:2439327 | AAGAATAAGGGAACA[A/G]TGAACTCTGCTGGGA | 899 |
rs116787796 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | CCNF | GRCh38.p7 | 16:2446657 | GGATAGGCTTGGCTG[C/T]ACACAGCATATGTGT | 899 |
rs116789260 | snp | A/G | 0.00291318 | 0.0380539 | intron-variant | CCNF | GRCh38.p7 | 16:2453360 | TGCTGGGGTGTGGGC[A/G]GGCCTCACCCTCGGG | 899 |
rs116939419 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant, downstream-variant-500B | CCNF | GRCh38.p7 | 16:2447559 | ATTGCACTGCAGCCT[A/G]GGCAATGGCGCAAGA | 899 |
rs117095504 | snp | A/G | 0.152778 | 0.230321 | intron-variant | CCNF | GRCh38.p7 | 16:2449767 | CACCACAGCCCCTCC[A/G]TCCCCTCCATCCCCT | 899 |
rs117232772 | snp | C/T | 0.00361289 | 0.0423485 | synonymous-codon | CCNF | GRCh38.p7 | 16:2455530 | CTCTGGCTATGAAGG[C/T]GACCAGGAGAGTGAG | 899 |
rs117246451 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2454161 | GGGTGGCTGGGTCTT[C/T]CCTGTCAATATAGGA | 899 |
rs117395112 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant, utr-variant-3-prime | CCNF | GRCh38.p7 | 16:2446748 | AGGTCATTGGCATGT[C/T]TTTTGTTTCATGAGG | 899 |
rs117691134 | snp | A/G | 9.80729e-05 | 0.00700192 | intron-variant | CCNF | GRCh38.p7 | 16:2449076 | TGGGAGGGCCTCATG[A/G]ACTCAGAGAGCAGCT | 899 |
rs117924154 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | CCNF | GRCh38.p7 | 16:2434169 | AAATTAGCTGGATGC[A/G]GTGATGGGCACTTGT | 899 |
rs118131564 | snp | A/T | 0.0101229 | 0.07042 | missense | CCNF | GRCh38.p7 | 16:2455489 | ACGCTGCTGGGCAGC[A/T]TCCTCGACTGGAGCC | 899 |
rs118173479 | snp | A/G | 0.00235605 | 0.0342414 | synonymous-codon | CCNF | GRCh38.p7 | 16:2455452 | TACCACCCCCACTGC[A/G]GAGCTGTCCAGCCAG | 899 |
rs137889833 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CCNF | GRCh38.p7 | 16:2436763 | TTAGAATATTCTCCT[C/T]GTCCCAAAAAGAACC | 899 |
rs137912941 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | CCNF, MIR6767 | GRCh38.p7 | 16:2445252 | AGGAACACAGTCGAA[A/G]GATGTGGGGCCTGCT | 899 |
rs137960953 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | CCNF | GRCh38.p7 | 16:2448331 | TGTGAGTCTGCCTAA[C/G]AGCCTTGCTGCTTTC | 899 |
rs138178557 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | CCNF | GRCh38.p7 | 16:2440028 | GAAGAGCTGGGAAAT[A/G]CGTTATTCATCTCTG | 899 |
rs138224180 | snp | A/G | 1.78261e-05 | 0.00298542 | missense, intron-variant | CCNF, LOC105371050 | GRCh38.p7 | 16:2456982 | CTATGCATACACAGT[A/G]AGGAGGAGGACATGA | 899 |
rs138243657 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | CCNF | GRCh38.p7 | 16:2455708 | CAGCTCCTGCCCCGC[C/T]GGGGAGTGTGTCCAG | 899 |
rs138327199 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | CCNF | GRCh38.p7 | 16:2432490 | CCTGGACACTCCTGC[G/T]TTGGCCCAGCGCTTA | 899 |
rs138459868 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | CCNF | GRCh38.p7 | 16:2454928 | AGCTGGGTGTGATGG[C/T]GGGCACCTGTAGTCC | 899 |
rs138583693 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CCNF | GRCh38.p7 | 16:2452177 | CGTCACCCAGGGCCT[C/T]GCTGTCCGGCTTCCA | 899 |
rs138778799 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2435881 | TGAAGGCCGTAAGTC[C/T]TCACCCCACCTGCAT | 899 |
rs138884988 | snp | C/T | 8.37009e-05 | 0.00646865 | intron-variant | CCNF | GRCh38.p7 | 16:2448809 | TCCGCCCCACCCCTG[C/T]CCCAGGAAGTGGGCT | 899 |
rs138913390 | snp | C/T | 4.97006e-05 | 0.00498476 | utr-variant-5-prime, missense | CCNF | GRCh38.p7 | 16:2437179 | GGCCTGAAGGCCTCT[C/T]GCTTCTTCAGTCTCG | 899 |
rs138971439 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2436494 | GCCTCCCACATTTGT[A/G]CTTCTAAACGATCTG | 899 |
rs139018313 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | CCNF | GRCh38.p7 | 16:2452742 | CCAGTAGTCTACTTT[C/T]TGTCCATGGATGTTT | 899 |
rs139107867 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, upstream-variant-2KB, intron-variant | CCNF, C16orf59, LOC105371050 | GRCh38.p7 | 16:2458432 | TTTTTGTATTTTCGG[C/T]AGAGACGGGATTTCA | 899 |
rs139143672 | snp | A/G | 3.29489e-05 | 0.00405874 | utr-variant-5-prime, missense, upstream-variant-2KB | CCNF, MIR6767 | GRCh38.p7 | 16:2443715 | AGAGCTTCCAGTGAG[A/G]TCGTCTGCCAGCTAT | 899 |
rs139261240 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2446371 | GTTAGAGAGTTTTTC[A/G]TCCCCCACTGGTGCC | 899 |
rs139303228 | snp | C/G | 1.73009e-05 | 0.00294111 | missense | CCNF | GRCh38.p7 | 16:2455511 | ACTGGAGCCTGGACT[C/G]CTGCTCTGGCTATGA | 899 |
rs139373868 | snp | A/G | 1.64871e-05 | 0.00287111 | synonymous-codon | CCNF | GRCh38.p7 | 16:2448870 | GTTTATCAGTAAAGA[A/G]ATCCTGACCATCCGG | 899 |
rs139442838 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CCNF | GRCh38.p7 | 16:2453897 | GTCACTCCCGGCACT[C/T]GAGCTGTGACCTGAG | 899 |
rs139489397 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CCNF | GRCh38.p7 | 16:2437471 | GCAGATATGGGGAAC[A/G]CATCTGGAAATCAGC | 899 |
rs139519274 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | CCNF | GRCh38.p7 | 16:2430255 | GAAGGATGGATAGAA[A/C]GGTAGATTTGTAGAT | 899 |
rs139582105 | snp | C/T | 0.00619443 | 0.0553068 | intron-variant | CCNF | GRCh38.p7 | 16:2449942 | CCGGGCGCAGAGGCT[C/T]ATGCCTGTAACCCCA | 899 |
rs139587469 | snp | C/T | 6.60447e-05 | 0.00574613 | missense, downstream-variant-500B | CCNF, MIR6767 | GRCh38.p7 | 16:2445546 | GTGGAGTGTGTGGAC[C/T]GGTACCTGCGGAGGA | 899 |
rs139608155 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CCNF | GRCh38.p7 | 16:2434605 | AACAGAGCGAGACTC[C/T]GTCTCAAAATAAATA | 899 |
rs139783276 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2437744 | TCTACAAAAAATACA[A/C]AAAAGTTAGCCAGGG | 899 |
rs139828844 | snp | A/G | 8.78418e-05 | 0.0066267 | missense | CCNF | GRCh38.p7 | 16:2455561 | GGCGAGAAGGAGGGC[A/G]ACGGTGAGTGTGGGG | 899 |
rs139948554 | snp | G/T | 0.0138799 | 0.0821421 | intron-variant | CCNF | GRCh38.p7 | 16:2441785 | GCCTCCCAAAGTGTT[G/T]GGATTACAGGAGTGA | 899 |
rs139949328 | snp | C/T | 0.00199481 | 0.0315187 | utr-variant-3-prime, intron-variant | CCNF, LOC105371050 | GRCh38.p7 | 16:2457653 | TGTCCCAGAGGCGTT[C/T]GTATGTGACCCACAG | 899 |
rs140236588 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | CCNF | GRCh38.p7 | 16:2448114 | CAGTCAGGATTCCTG[C/T]GGCCACACAGTGCCG | 899 |
rs140248806 | snp | C/T | 3.60568e-05 | 0.00424583 | intron-variant, synonymous-codon | CCNF | GRCh38.p7 | 16:2432996 | CCTGGTGGACAACCA[C/T]GCCAGTGTGTGGGCA | 899 |
rs140394912 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CCNF | GRCh38.p7 | 16:2450160 | TGCAGTGAGTTGATA[C/T]CACGTCACTGGACTC | 899 |
rs140447786 | in-del | -/T/TCCCCTCCATCCCCTCCC/TCCCCTCCC | 0.000189861 | 0.0097415 | intron-variant | CCNF | GRCh38.p7 | 16:2449803 | CCTCCATCCCCTCCA[lengthTooLong]CCCCTGGCCTGCTTT | 899 |
rs140456910 | snp | A/G | 6.61605e-05 | 0.00575116 | missense, nc-transcript-variant | CCNF, LOC105371050 | GRCh38.p7 | 16:2456911 | CATGTTTACAGTGTC[A/G]TCCCCCAAGTCCCCC | 899 |
rs140493876 | snp | A/C/G | 0.000183732 | 0.00958307 | utr-variant-5-prime, missense | CCNF | GRCh38.p7 | 16:2439455 | AGCGACAGGAGGACA[A/C/G]ATGTGAGTGGTGCCT | 899 |
rs140530762 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | CCNF | GRCh38.p7 | 16:2432163 | CAGTGAAATTTGCAT[C/G]CCTTAAAAAATAGGA | 899 |
rs140537659 | in-del | -/AT | | | intron-variant | CCNF | GRCh38.p7 | 16:2437854 | AATGAGCCGTGACTA[-/AT]TGCCAATGCACTCCA | 899 |
rs140562343 | snp | A/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2433896 | CCAGAAATCCAGATC[A/G]ACAGCCAACCAGGGC | 899 |
rs140563930 | snp | A/G | 1.6951e-05 | 0.00291122 | missense | CCNF | GRCh38.p7 | 16:2449399 | CACACCAGCCTGTCC[A/G]CCTACGCCCCAGCCC | 899 |
rs140770913 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime | CCNF | GRCh38.p7 | 16:2446923 | TGTAGTCTCTTCGGG[A/C]CTGTGTGTGCCAGCT | 899 |
rs140822341 | snp | A/C | 0.0103295 | 0.0711199 | intron-variant | CCNF | GRCh38.p7 | 16:2454558 | GCTCTCTCCACCCCC[A/C]GCCCTCCACCAGGCC | 899 |
rs140856384 | snp | A/G | 0.000610768 | 0.0174646 | utr-variant-5-prime, synonymous-codon | CCNF | GRCh38.p7 | 16:2435839 | TTTCGAAGCTGCTGT[A/G]AAGCTGGGCATAGCC | 899 |
rs140865437 | snp | C/T | 0.000271839 | 0.0116553 | intron-variant | CCNF | GRCh38.p7 | 16:2449513 | GGGAAGGTGCTGACA[C/T]AGGAGGAGGCTGTGG | 899 |
rs141102044 | in-del | -/TA | 0.0441095 | 0.141807 | intron-variant | CCNF | GRCh38.p7 | 16:2437852 | GCAATGAGCCGTGAC[-/TA]TATGCCAATGCACTC | 899 |
rs141201197 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2440814 | TACAAGAAGGCCAGA[C/T]GTGATGGCTCACGCC | 899 |
rs141266536 | snp | A/G | 0.000302984 | 0.0123045 | synonymous-codon | CCNF | GRCh38.p7 | 16:2455476 | CAGCCAGGAGGAGAC[A/G]CTGCTGGGCAGCTTC | 899 |
rs141290345 | in-del | -/TT | | | intron-variant, downstream-variant-500B | CCNF, MIR6767 | GRCh38.p7 | 16:2445726 | TGGTTTTGTTTTGTG[-/TT]TTGTTTTTTTTTTTT | 899 |
rs141420377 | snp | A/G | 0.00337045 | 0.0409129 | intron-variant | CCNF | GRCh38.p7 | 16:2455594 | AGGGTGCACCAGAAG[A/G]GACATCACACAGAGG | 899 |
rs141610633 | snp | C/T | 0.000247981 | 0.0111323 | utr-variant-5-prime, missense | CCNF | GRCh38.p7 | 16:2437200 | TTCAGTCTCGCTGAG[C/T]GGCTGAATGTGGGTG | 899 |
rs141718863 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | CCNF | GRCh38.p7 | 16:2433507 | ATGGTCCCAGGTACC[C/T]GCCGCCCTCAGAACA | 899 |
rs141747145 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CCNF | GRCh38.p7 | 16:2427934 | GGCTAATGTGCTCAT[A/G]GCTGGCTCTAGTTGA | 899 |
rs142081758 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | CCNF, LOC105371050 | GRCh38.p7 | 16:2457908 | TTCCCAGATAGGCTA[A/G]CCAGAAAAAACTTCA | 899 |
rs142132500 | snp | A/G | 3.34476e-05 | 0.00408934 | synonymous-codon | CCNF | GRCh38.p7 | 16:2449347 | GGAGCTGAGAACCCA[A/G]CACCTGTGCAGCTTC | 899 |
rs142188142 | snp | C/T | 0 | 0 | intron-variant | CCNF | GRCh38.p7 | 16:2453762 | GAGGCTATTGCCTCT[C/T]GCTCTGACTGGGCTC | 899 |
rs142241270 | snp | C/T | 3.29462e-05 | 0.00405857 | utr-variant-5-prime, synonymous-codon | CCNF | GRCh38.p7 | 16:2431164 | CAAGTGTTTCTGTTA[C/T]CCTACAAAGCGAAGA | 899 |
rs142249495 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CCNF | GRCh38.p7 | 16:2438902 | ACTTGGGAGGCTGAG[A/G]CATGAGAGTTGCTTG | 899 |
rs142389062 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CCNF | GRCh38.p7 | 16:2434992 | GAGCGTGGTGGCTCA[C/T]GCTTGTAATCCCAGC | 899 |
rs142455439 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CCNF | GRCh38.p7 | 16:2448526 | ATCCTCCCACCTTAG[C/T]GTCCCAAGTAACTGA | 899 |
rs142532028 | snp | C/T | 0.000578345 | 0.0169952 | missense, nc-transcript-variant | CCNF, LOC105371050 | GRCh38.p7 | 16:2456910 | TCATGTTTACAGTGT[C/T]GTCCCCCAAGTCCCC | 899 |
rs142557915 | snp | C/T | 0.00398564 | 0.0444627 | utr-variant-3-prime, upstream-variant-2KB, intron-variant | CCNF, C16orf59, LOC105371050 | GRCh38.p7 | 16:2458492 | TGACCTCAAGTGATC[C/T]GCCCACTTCGGTCTC | 899 |
rs142589897 | snp | C/G | 1.65318e-05 | 0.002875 | synonymous-codon | CCNF | GRCh38.p7 | 16:2453252 | CAGGCAAGTCTCTCT[C/G]ACCGCCGTGAAGCAG | 899 |
rs142661106 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | CCNF | GRCh38.p7 | 16:2454929 | GCTGGGTGTGATGGC[A/G]GGCACCTGTAGTCCC | 899 |
rs142675674 | snp | G/T | | | splice-donor-variant | CCNF | GRCh38.p7 | 16:2438125 | TGAGTCTGTTCGAGG[G/T]GAGTCAAGTTGTTCT | 899 |
rs142841189 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | CCNF | GRCh38.p7 | 16:2433297 | TCACGCCACTGACAC[A/G]GGCCCGTGGTGCCTC | 899 |
rs142891251 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | CCNF | GRCh38.p7 | 16:2436583 | ACCATGAGCAACACC[C/G]TCCTCCAGAATCAGG | 899 |
rs142923904 | snp | A/G | 8.31262e-05 | 0.00644641 | missense, downstream-variant-500B | CCNF, LOC105371050 | GRCh38.p7 | 16:2456772 | TCAGGGTACTCCTCC[A/G]TCAGCACCGCAAGTC | 899 |
rs142961190 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2453009 | TTCTGTGTGGACATA[A/G]TTTTTCCTTTTTCCT | 899 |
rs142970159 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | CCNF, MIR6767 | GRCh38.p7 | 16:2445298 | ACGGAGCCTCCCGGG[C/T]TTCCTGTGACATGGC | 899 |
rs142982582 | snp | C/T | 4.96438e-05 | 0.00498191 | missense | CCNF | GRCh38.p7 | 16:2453519 | TCCTCAGCTCTCCCT[C/T]GGGGCGGAGAACCAA | 899 |
rs143110704 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2436430 | AGCACCCCAAGGAAC[A/G]AGCCCATGATCTGTC | 899 |
rs143155692 | snp | C/G | 1.64754e-05 | 0.00287009 | utr-variant-5-prime, missense, upstream-variant-2KB | CCNF, MIR6767 | GRCh38.p7 | 16:2443735 | CTGCCAGCTATTTCA[C/G]GCTTCCCAGGCTGTC | 899 |
rs143566750 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2433464 | CCCAACCTGCACCCC[A/G]CACCCTGGCCCCTGT | 899 |
rs143849552 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2440198 | TTGAGAGCAGAGGGG[C/T]GTGGAGAGTCCCTTC | 899 |
rs143891459 | in-del | -/A | | | intron-variant | CCNF | GRCh38.p7 | 16:2450839 | CACCACGTGGCCCCC[-/A]GTCAGGAAAATACTC | 899 |
rs143974143 | snp | A/G | 0.000368114 | 0.0135618 | intron-variant, missense | CCNF | GRCh38.p7 | 16:2433046 | TGTGGCCGTCTCCAG[A/G]GAACCTGAAGCTCTT | 899 |
rs144015404 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2450199 | GTGACAGAGCAAGAC[C/T]CTGTCTCTAAAAACA | 899 |
rs144092255 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CCNF | GRCh38.p7 | 16:2452382 | TGCCTTCTGGGCAAG[A/G]AACGAGGCTGACAGT | 899 |
rs144142827 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | CCNF | GRCh38.p7 | 16:2454288 | TGCTGCTGCTTCCTC[C/T]CCAAGAAGCGTGACA | 899 |
rs144172354 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | CCNF | GRCh38.p7 | 16:2429954 | GTGGAAAGCAGCGTT[C/G]GGCCCCGCGCGCGTT | 899 |
rs144374996 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | CCNF | GRCh38.p7 | 16:2441615 | CTCAGCTCACTGCAA[A/C]CTCTGACGCCTGGGT | 899 |
rs144568021 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2455972 | AGGCTAGAAGTTCAA[A/G]ACCAGCCTGGGTGAC | 899 |
rs144631476 | snp | G/T | 0.000115908 | 0.00761188 | synonymous-codon, downstream-variant-500B | CCNF, MIR6767 | GRCh38.p7 | 16:2445575 | GAGGCTGGTGCCGCG[G/T]TACAGGCTCCAGCTG | 899 |
rs144671828 | snp | A/G | 1.65151e-05 | 0.00287355 | utr-variant-5-prime, missense | CCNF | GRCh38.p7 | 16:2435865 | TAGCCTACCTCTACA[A/G]TGAAGGCCGTAAGTC | 899 |
rs144735305 | snp | A/G | 3.31455e-05 | 0.00407083 | intron-variant | CCNF | GRCh38.p7 | 16:2453354 | ATGGGGTGCTGGGGT[A/G]TGGGCGGGCCTCACC | 899 |
rs144850622 | snp | C/T | 0.00701438 | 0.0588047 | intron-variant | CCNF | GRCh38.p7 | 16:2449155 | CGTCGCCATCTGCGC[C/T]GGTGCGCTACGCGTG | 899 |
rs144998617 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, utr-variant-3-prime | CCNF | GRCh38.p7 | 16:2447116 | CATCACTGCAACCTA[C/T]GACAAAGCTCCTGGG | 899 |
rs145125251 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2448712 | ACAGGCAGCTGGCTC[C/T]ATTATGAAGCCTCTG | 899 |
rs145199301 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CCNF | GRCh38.p7 | 16:2448325 | GACATTTGTGAGTCT[A/G]CCTAACAGCCTTGCT | 899 |
rs145266442 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant, utr-variant-3-prime | CCNF | GRCh38.p7 | 16:2446988 | AACCCTGCCACAAGC[A/C]TCCAGAGCTGTCTTC | 899 |
rs145333714 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | CCNF | GRCh38.p7 | 16:2446445 | CGTGCGTCCTTACAC[A/G]GCAGCCTGTCCTTTT | 899 |
rs145370728 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2434668 | CATTGGTTTTTAGTA[C/T]ACTGAGAGTTGTACA | 899 |
rs145373353 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | CCNF, MIR6767 | GRCh38.p7 | 16:2445132 | CCCGCTCCCTGCACG[C/G]CCCGAGGGTCAGGGT | 899 |
rs145432131 | snp | C/T | 0.0269805 | 0.11297 | intron-variant, upstream-variant-2KB | CCNF, MIR6767 | GRCh38.p7 | 16:2443622 | ATGGCTGCTGTCTCA[C/T]GCTCATGTTTGTCTT | 899 |
rs145521789 | snp | C/T | 8.38188e-05 | 0.0064732 | stop-gained, downstream-variant-500B | CCNF, LOC105371050 | GRCh38.p7 | 16:2456664 | GGACCCCAGGACCCA[C/T]AGGCACTGGCGCTGG | 899 |
rs145600387 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | CCNF | GRCh38.p7 | 16:2430884 | AGTTACATGACATGC[A/G]CTATTTGCCATAAAT | 899 |
rs145635947 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2450149 | GAAGCAGAGGTTGCA[A/G]TGAGTTGATATCACG | 899 |
rs145848123 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CCNF | GRCh38.p7 | 16:2432121 | AGGCATGAGCCACTG[C/T]ACCCGGCTGAAAGTA | 899 |
rs145924064 | snp | C/T | | | synonymous-codon, downstream-variant-500B | CCNF, MIR6767 | GRCh38.p7 | 16:2445545 | CGTGGAGTGTGTGGA[C/T]CGGTACCTGCGGAGG | 899 |
rs146026073 | snp | A/G | 1.72341e-05 | 0.00293543 | missense | CCNF | GRCh38.p7 | 16:2455531 | TCTGGCTATGAAGGC[A/G]ACCAGGAGAGTGAGG | 899 |
rs146030951 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | CCNF, LOC105371050 | GRCh38.p7 | 16:2457294 | CCTCTCTGTCCCTTC[C/T]GTGTCTCACTGTCTC | 899 |
rs146106729 | in-del | -/CT | | | intron-variant, upstream-variant-2KB | CCNF, MIR6767 | GRCh38.p7 | 16:2444984 | GTAACCTCTGCCTCG[-/CT]GGCTCAAGCCTTTCT | 899 |
rs146155135 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | CCNF | GRCh38.p7 | 16:2441781 | CTCGGCCTCCCAAAG[G/T]GTTGGGATTACAGGA | 899 |
rs146372164 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CCNF | GRCh38.p7 | 16:2440868 | TTGAGTTGGGAGGAT[C/T]GCTTGAGCCCAGGAG | 899 |
rs146413013 | in-del | -/CACACACACATATATATG | | | intron-variant | CCNF | GRCh38.p7 | 16:2435620 | ATATATATGCACACA[-/CACACACACATATATATG]CACACACATATATAT | 899 |
rs146438723 | snp | A/G | 0.00636585 | 0.0560571 | missense | CCNF | GRCh38.p7 | 16:2448977 | TGGAAGGGAAGATTC[A/G]AGTAAGCAGCGGTTC | 899 |
rs146508306 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2454383 | CTCCCTGGGGCCAGG[G/T]TCATCACGAGGAAAG | 899 |
rs146626160 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2438319 | CTGGCTCCATGACCC[A/G]CCTGGCAGGGGAGTG | 899 |
rs146684439 | snp | C/T | 0.00358779 | 0.0422022 | utr-variant-3-prime, upstream-variant-2KB, downstream-variant-500B, intron-variant | CCNF, C16orf59, LOC105371050 | GRCh38.p7 | 16:2458734 | TTGGAACTGTAGACC[C/T]GTCCTGTCGACTGTG | 899 |
rs147234069 | snp | A/G | 5.02374e-05 | 0.0050116 | utr-variant-5-prime, missense | CCNF | GRCh38.p7 | 16:2439765 | TGTCAGATCCTGGGC[A/G]ATGCCTCCACAGCTT | 899 |
rs147242999 | snp | C/G/T | 0.000946098 | 0.0217294 | missense, synonymous-codon | CCNF | GRCh38.p7 | 16:2449455 | GGCCAGACTGACGCA[C/G/T]GGGCAGAGTAAGGAG | 899 |
rs147276022 | in-del | -/AG | 0.00835141 | 0.0640778 | intron-variant, downstream-variant-500B | CCNF, LOC105371050 | GRCh38.p7 | 16:2456427 | ACAGGAGGGTAACAC[-/AG]GGGACCGTAGCAAGG | 899 |
rs147350163 | snp | A/C | 0.0232847 | 0.105357 | intron-variant | CCNF | GRCh38.p7 | 16:2434565 | GCAGTGAGCCGAGAT[A/C]GCACCACTGCACTCC | 899 |
rs147350588 | in-del | -/ACATATATATATATATAT | 0.404559 | 0.196498 | intron-variant | CCNF | GRCh38.p7 | 16:2435665 | TATATGCACACACAC[-/ACATATATATATATATAT]ATATATATATATATA | 899 |
rs147359389 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2436694 | CTAAAGCCTGCAATT[C/G]TGTGGTTTTTTAGGA | 899 |
rs147579473 | snp | A/G | 0.00159617 | 0.0282053 | utr-variant-3-prime, upstream-variant-2KB, intron-variant | CCNF, C16orf59, LOC105371050 | GRCh38.p7 | 16:2458464 | CATGTTGGCCAGGCT[A/G]GTCTCGAACTCATGA | 899 |
rs147684222 | snp | C/G | 1.65441e-05 | 0.00287607 | intron-variant, upstream-variant-2KB | CCNF, MIR6767 | GRCh38.p7 | 16:2443807 | CACAATGAGGTGAGG[C/G]ATTCAGGCCGGGGCT | 899 |
rs147693684 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | CCNF | GRCh38.p7 | 16:2446861 | ACATTCACCTTTGCA[C/T]TGAGCTTAGTCTTGT | 899 |
rs147731099 | snp | C/G | 1.6585e-05 | 0.00287962 | missense, downstream-variant-500B | CCNF, LOC105371050 | GRCh38.p7 | 16:2456791 | GCACCGCAAGTCCCA[C/G]AAGCTCCGTGGACGG | 899 |
rs147968073 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B, upstream-variant-2KB | CCNF, C16orf59, LOC105371050 | GRCh38.p7 | 16:2459149 | GGGCCAGAGCTGCCT[A/G]GGTCCCAACCTCCCT | 899 |
rs148030604 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CCNF | GRCh38.p7 | 16:2433495 | TCACATGTGCTCATG[A/G]TCCCAGGTACCCGCC | 899 |
rs148105729 | snp | C/G | 7.24008e-05 | 0.00601624 | missense | CCNF | GRCh38.p7 | 16:2455453 | ACCACCCCCACTGCG[C/G]AGCTGTCCAGCCAGG | 899 |
rs148159882 | snp | A/G | 8.5626e-05 | 0.0065426 | utr-variant-5-prime, missense | CCNF | GRCh38.p7 | 16:2437263 | CCGTGGTCGGTGAGC[A/G]GAAGCTGCTGCAAGG | 899 |
rs148212310 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | CCNF | GRCh38.p7 | 16:2451245 | GGCAGGTGGCGCGGG[C/T]GGGGGCGACTCCCTT | 899 |
rs148230210 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CCNF | GRCh38.p7 | 16:2440774 | ACATTGTGGTGTTCA[C/T]GTCCAAAAAGCCAGT | 899 |
rs148386337 | in-del | -/ATATATAATATATATATA | 0.313326 | 0.241847 | intron-variant | CCNF | GRCh38.p7 | 16:2443161 | TATATAATATATATT[-/ATATATAATATATATATA]ATATATAATATATAT | 899 |
rs148419125 | snp | A/G | 0.000734668 | 0.0191519 | missense, downstream-variant-500B | CCNF, LOC105371050 | GRCh38.p7 | 16:2456731 | TGGTCCGCACCAGCC[A/G]GGAGCCAGGGAAGGA | 899 |
rs148523749 | snp | A/C/T | 0.00247234 | 0.0350755 | intron-variant | CCNF | GRCh38.p7 | 16:2453562 | CCTGCGTTCTGGCTG[A/C/T]GCCATACAATGCTGG | 899 |
rs148573205 | snp | C/T | 0.00721501 | 0.0596276 | intron-variant | CCNF | GRCh38.p7 | 16:2449177 | CTACGCGTGCAGCAT[C/T]GGCGTGAACATCATC | 899 |
rs148774454 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | CCNF | GRCh38.p7 | 16:2434976 | TAAGAAATGTTCGAC[C/T]GAGCGTGGTGGCTCA | 899 |
rs148810003 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | CCNF, MIR6767 | GRCh38.p7 | 16:2445673 | GCTGGCCTTTCCCGG[C/G]TTCAGGGTCACCTGC | 899 |
rs148847295 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | CCNF | GRCh38.p7 | 16:2454789 | GAGGGGCCGGGTGCG[A/G]TTGCTCATGCCTGTA | 899 |
rs148977637 | snp | C/T | 1.65332e-05 | 0.00287512 | utr-variant-5-prime, synonymous-codon | CCNF | GRCh38.p7 | 16:2437193 | TCGCTTCTTCAGTCT[C/T]GCTGAGCGGCTGAAT | 899 |
rs149086596 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2435994 | TATCCGATGGCCTGC[C/T]TCCCCATTCCCTCTC | 899 |
rs149236423 | snp | A/C/T | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | CCNF, MIR6767 | GRCh38.p7 | 16:2445130 | CTCCCGCTCCCTGCA[A/C/T]GCCCCGAGGGTCAGG | 899 |
rs149458467 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2440059 | CCTATCCACTCTTGC[C/T]TCTCAGCCAGCCAAC | 899 |
rs149583622 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2455811 | AGGCCACACCTATCC[A/G]GCTCCTGCTCATTCC | 899 |
rs149600932 | snp | G/T | 2.10329e-05 | 0.00324284 | missense, intron-variant | CCNF, LOC105371050 | GRCh38.p7 | 16:2457014 | CCTGGGCCTTGTGAG[G/T]CTGTAAGTGTGTCAG | 899 |
rs149653783 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | CCNF | GRCh38.p7 | 16:2454628 | CTTTTCCCAGGCTCA[C/T]GCCCACACACTGGCC | 899 |
rs149659964 | snp | C/T | 3.69672e-05 | 0.0042991 | synonymous-codon, downstream-variant-500B | CCNF, LOC105371050 | GRCh38.p7 | 16:2456576 | CATCCTCGATGTCAC[C/T]GTGGTCTACCTGAAC | 899 |
rs149782877 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | CCNF | GRCh38.p7 | 16:2441814 | GAGCCACTGCACCTG[A/G]CCAAAAAAAATTAAT | 899 |
rs149826921 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | CCNF | GRCh38.p7 | 16:2437542 | GAGTTCTGGGTACAC[A/G]TGCTGACAGCTGGAA | 899 |
rs149898676 | snp | A/G | 0.0444908 | 0.142359 | intron-variant | CCNF | GRCh38.p7 | 16:2434606 | ACAGAGCGAGACTCC[A/G]TCTCAAAATAAATAA | 899 |
rs149900630 | snp | C/T | 0.0111196 | 0.0737302 | utr-variant-3-prime, upstream-variant-2KB, intron-variant | CCNF, C16orf59, LOC105371050 | GRCh38.p7 | 16:2458438 | TATTTTCGGTAGAGA[C/T]GGGATTTCACCATGT | 899 |
rs150074698 | in-del | -/CC | 0.0154538 | 0.0865337 | intron-variant | CCNF | GRCh38.p7 | 16:2440505 | CCTGATACTCAGGAA[-/CC]GTTGAGGCAGGAGAA | 899 |
rs150153245 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2439536 | CCTTGGATGCGTTTC[C/T]GTCCACAAAAGGGAG | 899 |
rs150266909 | snp | A/C | 0.00953873 | 0.0683987 | intron-variant | CCNF | GRCh38.p7 | 16:2431600 | CGGGAAAATTGCTTG[A/C]ACCTGGGAGGCAGAG | 899 |
rs150393278 | snp | C/G | 9.92359e-05 | 0.0070433 | missense, nc-transcript-variant | CCNF, LOC105371050 | GRCh38.p7 | 16:2456917 | TACAGTGTCGTCCCC[C/G]AAGTCCCCCGGAGAG | 899 |
rs150444428 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2451933 | TGCCACCCCCCTGCC[A/G]GCGTGACTCAGCCAA | 899 |
rs150447372 | snp | C/T | 0.000732969 | 0.0191297 | missense | CCNF | GRCh38.p7 | 16:2449414 | GCCTACGCCCCAGCC[C/T]GCCTGGCTGCCGCAG | 899 |
rs150541774 | snp | C/T | 7.18559e-05 | 0.00599356 | utr-variant-5-prime, synonymous-codon | CCNF | GRCh38.p7 | 16:2437280 | AAGCTGCTGCAAGGC[C/T]GTGGTTCACGAGAGC | 899 |
rs150571268 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CCNF | GRCh38.p7 | 16:2449637 | GACCATGAGCCTGCA[C/T]GCCCTATGTATGGGT | 899 |
rs150595466 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | CCNF | GRCh38.p7 | 16:2433743 | GGCACGCGCTACCAC[A/G]CCCATCTAATTTTTG | 899 |
rs150760364 | snp | C/T | 0.00358779 | 0.0422022 | upstream-variant-2KB, intron-variant | CCNF | GRCh38.p7 | 16:2428201 | TTCCCAACTTCCAGA[C/T]CCTCTCTGGGGCCAC | 899 |
rs150770898 | snp | C/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2453886 | ATGATGCTGCTGTCA[C/T]TCCCGGCACTCGAGC | 899 |
rs150822354 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | CCNF | GRCh38.p7 | 16:2455621 | GAGGGTGGCTCTCAC[C/T]GAGGGCCTCTGGGCA | 899 |
rs150834162 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | CCNF | GRCh38.p7 | 16:2446021 | AGGCACAAGCCACTG[C/T]GCCTGGCCCTCACTG | 899 |
rs150848033 | snp | C/T | 0.000429007 | 0.0146397 | synonymous-codon, downstream-variant-500B | CCNF, MIR6767 | GRCh38.p7 | 16:2445524 | AAGCCTGTGCCTGCA[C/T]CTGACCGTGGAGTGT | 899 |
rs151088729 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | CCNF | GRCh38.p7 | 16:2430950 | GTAATTTGTGCAATG[A/C]CACTCCTTTACATAA | 899 |
rs151141585 | snp | C/T | 0.00597247 | 0.0543191 | utr-variant-3-prime, intron-variant | CCNF, LOC105371050 | GRCh38.p7 | 16:2457995 | CGTGTCCTGGCTGAT[C/T]CCAACTGCAGCTCTG | 899 |
rs151164394 | snp | C/T | 0.000585299 | 0.017097 | synonymous-codon | CCNF | GRCh38.p7 | 16:2449350 | GCTGAGAACCCAGCA[C/T]CTGTGCAGCTTCCTC | 899 |
rs151214953 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | CCNF | GRCh38.p7 | 16:2447789 | GGCTGAGCTGCCCCC[A/C/T]ACCTCTGCTCTCAGA | 899 |
rs151217933 | snp | A/G | 0.00351903 | 0.0417987 | utr-variant-5-prime, synonymous-codon | CCNF | GRCh38.p7 | 16:2431224 | CTTGAGTCTCCCCGA[A/G]GATGTGCTCTTTCAC | 899 |
rs180707939 | snp | A/C/G | 4.96507e-05 | 0.0049823 | synonymous-codon, downstream-variant-500B | CCNF, MIR6767 | GRCh38.p7 | 16:2445479 | TCTGATCGACTGGCT[A/C/G]GTGGAAGTTGCCACC | 899 |
rs181011369 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | CCNF | GRCh38.p7 | 16:2442168 | TGCACCACCACGCCC[A/G]GCTAAATTTTTTGTA | 899 |
rs181021092 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | CCNF | GRCh38.p7 | 16:2432072 | CTTGACCTCGTGATC[C/T]GCCCGCCTCGGCCTC | 899 |
rs181025821 | snp | C/T | 0.000550601 | 0.016583 | intron-variant | CCNF | GRCh38.p7 | 16:2449271 | GCCCACACCCCGTCC[C/T]GGCTGTCTAGGTCCC | 899 |
rs181270515 | snp | A/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2442567 | TATATAATATTATAT[A/T]ATATAATATTATTAT | 899 |
rs181326448 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2450316 | CCAACCTGGTCAACG[A/T]GGCAAAACCCTGTCT | 899 |
rs181441047 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CCNF | GRCh38.p7 | 16:2442039 | TTGATGGAGTCTTGC[A/T]CTGTTGCCCAGGCTG | 899 |
rs181460056 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | CCNF | GRCh38.p7 | 16:2432338 | ATGGGGAAATGCCAG[C/G]AAGAACCCATTTTCT | 899 |
rs181474080 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B, upstream-variant-2KB, nc-transcript-variant | CCNF, C16orf59, LOC105371050 | GRCh38.p7 | 16:2458927 | AACTCTGCATGGAGT[C/T]AGTTCTCTGCTTTCT | 899 |
rs181508506 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CCNF | GRCh38.p7 | 16:2433648 | CTGGAGTGCAGTGGT[A/G]CAATCTCAGCTCACT | 899 |
rs181618361 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | CCNF, MIR6767 | GRCh38.p7 | 16:2445746 | TTTTTTTTTTTTCCC[G/T]AGACCAAGTCTCGCT | 899 |
rs181629025 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2450649 | CCTGACCCGTGGTAA[A/C]TTGTGCGTGTTGTCA | 899 |
rs181898681 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2453603 | CCGGCCCAGTTCCCT[C/T]AGCGCTTCCTCACAC | 899 |
rs181967550 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CCNF | GRCh38.p7 | 16:2437654 | AGCACTTTGGGAGGC[A/C]GAGGCTGGAGAATTG | 899 |
rs181988754 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CCNF | GRCh38.p7 | 16:2454298 | TCCTCCCCAAGAAGC[A/G]TGACAGCACTTTCCA | 899 |
rs182167548 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CCNF | GRCh38.p7 | 16:2437070 | CCAAGACCATGGAGA[A/G]CTTTCCACATTCCGT | 899 |
rs182187641 | snp | C/T | 0.000369599 | 0.0135891 | intron-variant, upstream-variant-2KB | CCNF, MIR6767 | GRCh38.p7 | 16:2443845 | AGAGCGGCGCGGAAG[C/T]CAGCCTCCAGGGGAA | 899 |
rs182254632 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CCNF | GRCh38.p7 | 16:2427689 | GAAACGGGCCCACAC[C/T]CTGGAGGAGCCACTT | 899 |
rs182262642 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant, downstream-variant-500B | CCNF | GRCh38.p7 | 16:2447318 | GACCAGGCACGGTGG[C/T]TCACGCCTGTAATCC | 899 |
rs182382278 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2434077 | TTGGGAGGCCAAGGC[A/G]GGTGGATCACTTGAG | 899 |
rs182386024 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CCNF | GRCh38.p7 | 16:2438382 | GGAGGCATCGAACCT[C/T]GATGCTCACTCGTCT | 899 |
rs182421386 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | CCNF | GRCh38.p7 | 16:2451109 | GCTTCCCTTCAGCCC[A/G]CGTTGGTTTGTTCCA | 899 |
rs182817534 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2455311 | CAGGCTGGGGCACGC[A/G]GGTGTTAGAGGCAGG | 899 |
rs182865872 | snp | A/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2442714 | ATTATATATAAATAT[A/G]TATTTATATATTGTA | 899 |
rs182878285 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | CCNF | GRCh38.p7 | 16:2435510 | GAATGGCTTAAGCCC[A/C]GGAGGTTGAGGCTGC | 899 |
rs182981048 | snp | A/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2442931 | TATATTAATATATAT[A/G]ATTATTATATATTAT | 899 |
rs183008387 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2438826 | ATGTGTTGAAACCAC[A/G]TCTTTACTAAAAAAC | 899 |
rs183018303 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2452217 | CAGAACTCCCTGGGG[G/T]TCTCGATGCCCTTGA | 899 |
rs183239891 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CCNF | GRCh38.p7 | 16:2455897 | GGAGATCCTTCTAGG[C/T]CTGTAGTCTCATGCC | 899 |
rs183262744 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | CCNF | GRCh38.p7 | 16:2440132 | ATTTGTGCCATTCTT[C/G]AAAGTTGTCCCATAG | 899 |
rs183355106 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2434893 | GCTTCTTTCACGGAC[A/C]CTGATGTTTTCAAGG | 899 |
rs183559779 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | CCNF | GRCh38.p7 | 16:2432081 | GTGATCCGCCCGCCT[C/T]GGCCTCCCAAAGTGC | 899 |
rs183565847 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CCNF | GRCh38.p7 | 16:2449589 | GGGTGAGATACAGCA[C/T]GGCTCCTACCTTCAG | 899 |
rs183586946 | snp | A/G | 0.000399281 | 0.0141238 | synonymous-codon | CCNF | GRCh38.p7 | 16:2455482 | GGAGGAGACGCTGCT[A/G]GGCAGCTTCCTCGAC | 899 |
rs183681445 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2452694 | AGCTGTCACCCTCCC[A/G]TTCCCCCCAACTTCC | 899 |
rs183962468 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2446346 | TGCCAGAGTTTCCTA[C/T]ACTCTTGGAGTTAGA | 899 |
rs184017595 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CCNF | GRCh38.p7 | 16:2441444 | GTAGTTCTCGTGGAA[A/G]TTCAAGGGGCCTCAG | 899 |
rs184054887 | snp | A/C | 0.00716266 | 0.059414 | utr-variant-3-prime, intron-variant | CCNF, LOC105371050 | GRCh38.p7 | 16:2458020 | GCTCTGCTGTGGGGG[A/C]CCGTGGGAGGGAGGC | 899 |
rs184183907 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | CCNF, MIR6767 | GRCh38.p7 | 16:2443436 | GGCCACTGACATTTC[A/G]TTATATATCTTTTCT | 899 |
rs184325082 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CCNF | GRCh38.p7 | 16:2440634 | GAATCAAAGAAAGCT[C/T]CTATTTGCCAAATGG | 899 |
rs184457545 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2456304 | GGTTGCTTGCTTCTG[C/T]GTCCACTTGGCTTGA | 899 |
rs184563660 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | CCNF | GRCh38.p7 | 16:2452908 | ATAATATTCCCCTGC[A/C]TGGACCACATGTGTT | 899 |
rs184578609 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | CCNF | GRCh38.p7 | 16:2436289 | AGCCAGGCTTCTAAA[C/T]GGGAAGCAGGTACAG | 899 |
rs184746860 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2448128 | GCGGCCACACAGTGC[C/G]GGGCACAGACTTTCC | 899 |
rs184804277 | snp | C/T | 0.000116045 | 0.00761636 | intron-variant | CCNF | GRCh38.p7 | 16:2453547 | CAAACGGTTAGTTAC[C/T]CTGCGTTCTGGCTGC | 899 |
rs184933003 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | CCNF | GRCh38.p7 | 16:2436934 | GATCACAATGACCCA[C/T]CTGTTCTAGACATTA | 899 |
rs184941836 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CCNF | GRCh38.p7 | 16:2454710 | ACCGCCCAAGGCCAG[A/G]CCATTCCATGCAATC | 899 |
rs185081490 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B, upstream-variant-2KB | CCNF, C16orf59, LOC105371050 | GRCh38.p7 | 16:2459211 | GCGATGGCACCTTCC[C/T]ATTAACGACTATGGA | 899 |
rs185086673 | snp | C/G/T | 0.000400643 | 0.0141483 | intron-variant, upstream-variant-2KB | CCNF, MIR6767 | GRCh38.p7 | 16:2443834 | GGCTTCTAATCAGAG[C/G/T]GGCGCGGAAGCCAGC | 899 |
rs185243642 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2434248 | CAGGTGGAGGTTGCA[A/G]TGAGCCAAGATTGCG | 899 |
rs185288878 | snp | A/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2442587 | AATATTATTATATAT[A/T]ATATATAATATTATA | 899 |
rs185301736 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2429949 | GCTCTGTGGAAAGCA[A/G]CGTTCGGCCCCGCGC | 899 |
rs185375254 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CCNF | GRCh38.p7 | 16:2451606 | CCCAGGCTGGAGTGC[A/G]GTGGCACCATCCTAG | 899 |
rs185577412 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CCNF, MIR6767 | GRCh38.p7 | 16:2444751 | ACAGATGCACACCAC[C/T]ATGCACAGCTAATTG | 899 |
rs185599843 | snp | C/T | 6.15505e-05 | 0.0055472 | intron-variant | CCNF | GRCh38.p7 | 16:2449097 | GAGAGCAGCTGTCTC[C/T]GCTGTGCCCAAAGCC | 899 |
rs185695813 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2431406 | GGCAGAGGCCAGGCA[C/T]GGTGGCTCATGCCTT | 899 |
rs186002048 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2437437 | CCTAAGGGAAGTGAA[C/G]ATGCAGAAAACTGAG | 899 |
rs186006935 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | CCNF | GRCh38.p7 | 16:2453849 | CCGTGCCTGTCATGC[A/G]CGTCCTGGACTTCTC | 899 |
rs186251518 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2432736 | TCCTCCTTCCCAGAT[C/G]ATTGTCCTCTGCCCT | 899 |
rs186292694 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2454976 | GAGGCAGGAGACTCA[C/G]TTGAACCCGGGAGGT | 899 |
rs186342694 | snp | C/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2437686 | TTGTGGCCAGGTGTT[C/T]GAGACCAGTCTGGGC | 899 |
rs186390448 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | CCNF | GRCh38.p7 | 16:2450419 | AGGAGGCTGAGACAG[C/G]AGAATCACTTGAACC | 899 |
rs186465450 | snp | C/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2442074 | GCAGTGGCACAATCT[C/T]GGCTCACCACAAGCT | 899 |
rs186558357 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CCNF | GRCh38.p7 | 16:2433734 | AGGATTACAGGCACG[C/T]GCTACCACGCCCATC | 899 |
rs186677755 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | CCNF, MIR6767 | GRCh38.p7 | 16:2445747 | TTTTTTTTTTTCCCG[A/T]GACCAAGTCTCGCTC | 899 |
rs186754506 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2438469 | AAATGGTGAAACCAC[A/G/T]TCTTTACTAAAAAAC | 899 |
rs187015836 | snp | C/T | 0.00795532 | 0.062565 | intron-variant, upstream-variant-2KB | CCNF, MIR6767 | GRCh38.p7 | 16:2443489 | AAAAGGAATAATAAT[C/T]AAAACCTGAGCCATC | 899 |
rs187329364 | snp | A/G | | | upstream-variant-2KB, intron-variant | CCNF | GRCh38.p7 | 16:2428760 | CCCAGCGTCAGCTCC[A/G]ACCTCCTCTTTCTCT | 899 |
rs187337068 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2447834 | ACCAGCCATCTCACA[C/T]CCCACGCTGGGCTCT | 899 |
rs187422644 | snp | A/G | 0.000198515 | 0.00996082 | intron-variant | CCNF | GRCh38.p7 | 16:2455582 | GAGTGTGGGGCCAGG[A/G]TGCACCAGAAGGGAC | 899 |
rs187435379 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CCNF | GRCh38.p7 | 16:2438953 | TAGTTAGCCAAGATC[A/G]TGCCACTATACTTTG | 899 |
rs187562850 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CCNF | GRCh38.p7 | 16:2456034 | GGCATCGTGGCGTGC[A/G]CCTGTGGTCCCAGCT | 899 |
rs187792410 | snp | A/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2434984 | GTTCGACCGAGCGTG[A/G]TGGCTCACGCTTGTA | 899 |
rs187867648 | snp | A/G | 0.000668684 | 0.0182728 | intron-variant | CCNF | GRCh38.p7 | 16:2435759 | GTAGTAGTTCATAAC[A/G]TTTGTGGCATAAAAT | 899 |
rs187876184 | snp | A/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2452750 | CTACTTTCTGTCCAT[A/G]GATGTTTCCCATTCT | 899 |
rs188232864 | snp | A/G | 0.00403771 | 0.0447499 | intron-variant | CCNF | GRCh38.p7 | 16:2453367 | GTGTGGGCGGGCCTC[A/G]CCCTCGGGGCCTCTG | 899 |
rs188248345 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | CCNF | GRCh38.p7 | 16:2436382 | AGAAACTTGCGCAGC[A/C]TTTTCTTCTACCAGT | 899 |
rs188468924 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CCNF | GRCh38.p7 | 16:2448221 | TATAACATTTCTACC[C/T]CACTGATAGAGCTGT | 899 |
rs188626640 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2440346 | TGTTAGGGCCAGGTG[C/T]GGTGGCTCACGCCTG | 899 |
rs188668905 | snp | C/T | 0.000576782 | 0.0169723 | intron-variant | CCNF | GRCh38.p7 | 16:2449954 | GCTCATGCCTGTAAC[C/T]CCAGCACTTTGGGAG | 899 |
rs188683684 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2432272 | TATTTTCTAGATATT[A/G]GAACCATAGGCTTAC | 899 |
rs188866309 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | CCNF | GRCh38.p7 | 16:2446913 | AACTGGGAGGTGTAG[C/T]CTCTTCGGGCCTGTG | 899 |
rs188936670 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | CCNF | GRCh38.p7 | 16:2453850 | CGTGCCTGTCATGCG[C/T]GTCCTGGACTTCTCT | 899 |
rs189087229 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B, upstream-variant-2KB, nc-transcript-variant | CCNF, C16orf59, LOC105371050 | GRCh38.p7 | 16:2458900 | GCCCCTTGTCCAGGG[C/G]CTCTTAATCCCAACT | 899 |
rs189194179 | snp | A/G | 0.000132851 | 0.00814909 | intron-variant, nc-transcript-variant | CCNF, MIR6767 | GRCh38.p7 | 16:2445454 | CGTGCTTCTCTTTCC[A/G]CAGGTACATTCTGAT | 899 |
rs189291369 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | CCNF | GRCh38.p7 | 16:2431900 | CAGTAGCGCAATCTC[A/G]GCTCACTGCAAGTTC | 899 |
rs189295282 | snp | C/T | 0.000655082 | 0.0180862 | intron-variant | CCNF | GRCh38.p7 | 16:2449244 | GCACCAAGGAGCCCC[C/T]GAGCGCTGAGAGCCC | 899 |
rs189523069 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2436974 | GGGGAGAAAAGACAG[A/G]TGCCCCCATCCTGGA | 899 |
rs189592797 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | CCNF | GRCh38.p7 | 16:2437541 | GGAGTTCTGGGTACA[C/T]GTGCTGACAGCTGGA | 899 |
rs189703997 | snp | A/G | 0.00306056 | 0.0389989 | utr-variant-3-prime, intron-variant | CCNF, LOC105371050 | GRCh38.p7 | 16:2457053 | CCGCAGTGGATGTGT[A/G]CTGAGGGGGCTGGAG | 899 |
rs189742397 | snp | C/G | 0.0107246 | 0.0724382 | intron-variant | CCNF | GRCh38.p7 | 16:2451917 | CATCTCAACCTTGAC[C/G]TGCCACCCCCCTGCC | 899 |
rs189803829 | snp | A/C/T | 0.000334291 | 0.0129244 | intron-variant | CCNF | GRCh38.p7 | 16:2453589 | CTGGCATCCTCGTGC[A/C/T]GGCCCAGTTCCCTCA | 899 |
rs189879148 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | CCNF | GRCh38.p7 | 16:2446986 | CAAACCCTGCCACAA[A/G]CATCCAGAGCTGTCT | 899 |
rs189945479 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CCNF | GRCh38.p7 | 16:2441060 | AATGTGGTGAAACCC[C/T]GTCTTTACTAAAAAT | 899 |
rs189995213 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CCNF | GRCh38.p7 | 16:2450568 | TTTTCACATTGAGAG[C/T]AGCTGCTCCCAACCC | 899 |
rs190102717 | snp | C/T | 5.00104e-05 | 0.00500027 | synonymous-codon, downstream-variant-500B | CCNF, MIR6767 | GRCh38.p7 | 16:2445599 | CCAGCTGCTGGGCAT[C/T]GCCTGCATGGTCATC | 899 |
rs190345807 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CCNF | GRCh38.p7 | 16:2442091 | GCTCACCACAAGCTC[C/T]GCCTCCTGGGTTCAT | 899 |
rs190543774 | snp | A/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2442658 | AATATTATTATATAT[A/T]ATATATAATATTATA | 899 |
rs190632938 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, downstream-variant-500B, upstream-variant-2KB | CCNF, C16orf59, LOC105371050 | GRCh38.p7 | 16:2459339 | TTAACACCAACTACA[C/T]GGGGCCCTGCTGCCT | 899 |
rs190643724 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2434514 | TATTCAGGAGGCTGA[A/G]GCAGGAGAATTGCTT | 899 |
rs190773640 | snp | A/G/T | 0.00102332 | 0.022597 | intron-variant, upstream-variant-2KB | CCNF, MIR6767 | GRCh38.p7 | 16:2443838 | TCTAATCAGAGCGGC[A/G/T]CGGAAGCCAGCCTCC | 899 |
rs190822428 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2455267 | ACCGGCATCTTCTTC[A/G/T]TAGCAGAACCTTTGG | 899 |
rs190902829 | snp | C/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2442506 | ATAATATAATATTAT[C/T]ATATATAATATATAA | 899 |
rs191021221 | snp | C/G | 0.0170251 | 0.090679 | intron-variant | CCNF | GRCh38.p7 | 16:2450966 | TTGCGCCGTCGTGCC[C/G]GGATGTGACCCCCTG | 899 |
rs191041595 | snp | G/T | 0.00447271 | 0.0470781 | intron-variant | CCNF | GRCh38.p7 | 16:2438155 | TCTGCACTGGGACTT[G/T]GTGTTCGATACATCC | 899 |
rs191093580 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2438645 | GACTCAGTCTCAGAA[A/G]AAAAAAAAAAAAGTA | 899 |
rs191312845 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | CCNF, MIR6767 | GRCh38.p7 | 16:2443412 | CTGAGACCTGAGCCA[C/T]GGTGGAAAGGCCACT | 899 |
rs191346450 | snp | C/T | 0.00328831 | 0.0404146 | synonymous-codon | CCNF | GRCh38.p7 | 16:2455461 | CACTGCGGAGCTGTC[C/T]AGCCAGGAGGAGACG | 899 |
rs191688502 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | CCNF | GRCh38.p7 | 16:2446128 | GGTGGCAGAACAGCC[A/T]TCAGCGTGTGGGGGC | 899 |
rs191718527 | snp | A/G/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2441125 | TAGAGTCCCAGCTAC[A/G/T]CGGGAGGCTGAGGCA | 899 |
rs191728753 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2447869 | GGCCACTGACATCTT[C/G]TCTTTTTGGCGTCTG | 899 |
rs191881140 | snp | A/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2442890 | ATATTATAATTATAT[A/G]TTATATATTATATAA | 899 |
rs191891396 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2433425 | ATTCTATCCTATAGC[A/G]TTTCACTCACTGGCT | 899 |
rs191963214 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | CCNF | GRCh38.p7 | 16:2455816 | ACACCTATCCGGCTC[C/G]TGCTCATTCCGTGTT | 899 |
rs191983251 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2440063 | TCCACTCTTGCCTCT[C/T]AGCCAGCCAACCTCT | 899 |
rs192155372 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CCNF | GRCh38.p7 | 16:2436542 | AGTCCCTACCTGGCC[A/G]GCTGGCAGAATTGTG | 899 |
rs192314535 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, missense, upstream-variant-2KB | CCNF, MIR6767 | GRCh38.p7 | 16:2443668 | CTTTAGCCAAAGCCT[A/G]TGCAAATGCAAACCA | 899 |
rs192421999 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | CCNF | GRCh38.p7 | 16:2452776 | ATTCTGTACATTCCA[C/T]ATAAATGGCGTCATC | 899 |
rs192437539 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | CCNF | GRCh38.p7 | 16:2436189 | GTGCGCCATGAGCAC[A/G]CAGACCTGCCTGTGG | 899 |
rs192481968 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2456253 | CTGCGGGGTCCTTGC[C/T]AGAAGCCCAGTTAGT | 899 |
rs192518497 | snp | C/T | 0.000911494 | 0.0213288 | intron-variant | CCNF | GRCh38.p7 | 16:2453372 | GGCGGGCCTCACCCT[C/T]GGGGCCTCTGCACCC | 899 |
rs192801071 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CCNF | GRCh38.p7 | 16:2440393 | GGAGGCCAAGGTGGG[C/T]GGATGACCTGAGGTC | 899 |
rs192845060 | snp | A/G | 0.000148394 | 0.00861248 | utr-variant-5-prime, missense | CCNF | GRCh38.p7 | 16:2431276 | GAGGACATCCTGGCC[A/G]TCCGAGCTGTAAGTC | 899 |
rs192864152 | snp | A/G | 0.0722614 | 0.17581 | intron-variant | CCNF | GRCh38.p7 | 16:2429799 | ATCGGGTCCCGGGGC[A/G]GCGATCGGGTCTCGG | 899 |
rs192944609 | snp | C/G | 0.00159617 | 0.0282053 | utr-variant-3-prime, intron-variant | CCNF, LOC105371050 | GRCh38.p7 | 16:2457848 | AACAAAAATCTTACT[C/G]CAGCCCCTCAATGCC | 899 |
rs192987045 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2452497 | TCTGGGCTGCGTTTA[C/T]TCTCTTCCTCCTGAA | 899 |
rs193020110 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | CCNF | GRCh38.p7 | 16:2449038 | TGCTGGAGGGTGGGG[G/T]TGGGCATTCAGCTTT | 899 |
rs193163268 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CCNF | GRCh38.p7 | 16:2435167 | GAGGCAGGAGAATGG[C/T]GTGAACCTGGGAGGC | 899 |
rs199502728 | snp | A/C | 0.00199792 | 0.0315431 | missense, nc-transcript-variant | CCNF, LOC105371050 | GRCh38.p7 | 16:2456922 | TGTCGTCCCCCAAGT[A/C]CCCCGGAGAGCAGTG | 899 |
rs199743115 | snp | C/T | 8.28096e-05 | 0.00643412 | missense | CCNF | GRCh38.p7 | 16:2453536 | GGGCGGAGAACCAAA[C/T]GGTTAGTTACCCTGC | 899 |
rs199744155 | in-del | -/T | | | upstream-variant-2KB, intron-variant | CCNF | GRCh38.p7 | 16:2428744 | TCCGCGGGGGAGACT[-/T]CCCAGCGTCAGCTCC | 899 |
rs199750563 | snp | G/T | 3.31631e-05 | 0.00407191 | missense, downstream-variant-500B | CCNF, MIR6767 | GRCh38.p7 | 16:2445581 | GGTGCCGCGGTACAG[G/T]CTCCAGCTGCTGGGC | 899 |
rs199799224 | snp | C/T | 0.000143051 | 0.00845607 | intron-variant | CCNF | GRCh38.p7 | 16:2437083 | GAGCTTTCCACATTC[C/T]GTCCCTAAGAGACAT | 899 |
rs199846397 | snp | C/T | 0.000136698 | 0.00826623 | intron-variant | CCNF | GRCh38.p7 | 16:2439835 | AGCGCAGGTGAGGTG[C/T]GGGGCTGGGATGACG | 899 |
rs199857541 | snp | C/T | 1.67978e-05 | 0.00289804 | synonymous-codon | CCNF | GRCh38.p7 | 16:2449368 | GTGCAGCTTCCTCTG[C/T]GAGCTCTCCCTGCTG | 899 |
rs199894140 | snp | C/T | 1.83818e-05 | 0.0030316 | synonymous-codon | CCNF | GRCh38.p7 | 16:2455434 | AGACAGAGGCAGCTT[C/T]GTTACCACCCCCACT | 899 |
rs200091447 | snp | C/T | 3.35599e-05 | 0.00409619 | intron-variant | CCNF | GRCh38.p7 | 16:2449025 | TTCGTTGTCGCTGTG[C/T]TGGAGGGTGGGGGTG | 899 |
rs200106833 | snp | A/G | 1.64811e-05 | 0.00287059 | intron-variant | CCNF | GRCh38.p7 | 16:2438143 | GTCAAGTTGTTCTCT[A/G]CACTGGGACTTTGTG | 899 |
rs200166258 | snp | A/G | 3.37963e-05 | 0.0041106 | missense, downstream-variant-500B | CCNF, LOC105371050 | GRCh38.p7 | 16:2456643 | GAGGCTTGTCCAGAG[A/G]ACAAGGGACCCCAGG | 899 |
rs200209194 | snp | C/T | 5.82044e-05 | 0.00539433 | synonymous-codon, downstream-variant-500B | CCNF, LOC105371050 | GRCh38.p7 | 16:2456558 | AGTGACAGCTCCCAG[C/T]GGCATCCTCGATGTC | 899 |
rs200223187 | snp | C/T | 0.00199792 | 0.0315431 | utr-variant-5-prime, missense | CCNF | GRCh38.p7 | 16:2431259 | TGAAATGGCTTTCTG[C/T]AGAGGACATCCTGGC | 899 |
rs200292802 | snp | C/G | 1.81266e-05 | 0.00301048 | intron-variant | CCNF | GRCh38.p7 | 16:2449481 | AGGAGTGGCCCTTCC[C/G]AGGGATGCCTGTGTC | 899 |
rs200331327 | snp | A/G | 0.00199792 | 0.0315431 | utr-variant-5-prime, missense | CCNF | GRCh38.p7 | 16:2435856 | AGCTGGGCATAGCCT[A/G]CCTCTACAATGAAGG | 899 |
rs200448070 | snp | A/G | 0.000206359 | 0.0101556 | intron-variant | CCNF | GRCh38.p7 | 16:2432918 | GTGTGGGGCTTTTGG[A/G]TGGTGCCTCCATCAC | 899 |
rs200485108 | snp | A/G | | | intron-variant, missense | CCNF | GRCh38.p7 | 16:2433066 | CTGAAGCTCTTTGAA[A/G]GGTATCTCTGCACCC | 899 |
rs200540114 | snp | C/T | 0.000314791 | 0.0125418 | utr-variant-5-prime, synonymous-codon | CCNF | GRCh38.p7 | 16:2437223 | TGTGGGTGCCGCACC[C/T]TTCATCTGGCTCTTC | 899 |
rs200540209 | snp | A/T | 0.000644122 | 0.0179345 | missense, nc-transcript-variant | CCNF, LOC105371050 | GRCh38.p7 | 16:2456869 | GTGACTCGCACACAC[A/T]GCCCTGCCACCATCA | 899 |
rs200571246 | snp | C/T | 0.0032255 | 0.0400293 | intron-variant | CCNF | GRCh38.p7 | 16:2453340 | CACCTGGGCGTCTCA[C/T]GGGGTGCTGGGGTGT | 899 |
rs200658437 | snp | A/G | 0.00195776 | 0.0312257 | intron-variant | CCNF | GRCh38.p7 | 16:2438021 | GGAGTGGTGGCCCCC[A/G]GGCAGTTCTCTGTGC | 899 |
rs200662201 | in-del | -/G | | | intron-variant, downstream-variant-500B | CCNF, MIR6767 | GRCh38.p7 | 16:2445729 | GTTTTGTTTTGTGTT[-/G]TTTTTTTTTTTTTCC | 899 |
rs200670134 | snp | A/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2434092 | GGGTGGATCACTTGA[A/G]GTCGGGAGTTCGAGA | 899 |
rs200870073 | snp | A/G | 0.00236381 | 0.0342975 | intron-variant, upstream-variant-2KB | CCNF, MIR6767 | GRCh38.p7 | 16:2443623 | TGGCTGCTGTCTCAC[A/G]CTCATGTTTGTCTTT | 899 |
rs200891175 | snp | A/G | 0.000122336 | 0.00782004 | synonymous-codon | CCNF | GRCh38.p7 | 16:2449452 | CCTGGCCAGACTGAC[A/G]CACGGGCAGAGTAAG | 899 |
rs200908912 | snp | A/C | 0.00013235 | 0.00813371 | missense | CCNF | GRCh38.p7 | 16:2453515 | GCCTTCCTCAGCTCT[A/C]CCTCGGGGCGGAGAA | 899 |
rs200973445 | snp | A/G/T | 1.64735e-05 | 0.00286993 | utr-variant-5-prime, missense | CCNF | GRCh38.p7 | 16:2431175 | GTTATCCTACAAAGC[A/G/T]AAGAATAAGGAGGAG | 899 |
rs200978756 | snp | C/T | 0.000281357 | 0.0118575 | utr-variant-5-prime, synonymous-codon | CCNF | GRCh38.p7 | 16:2437217 | GCTGAATGTGGGTGC[C/T]GCACCTTTCATCTGG | 899 |
rs201038398 | snp | C/T | 1.73069e-05 | 0.00294162 | missense, downstream-variant-500B | CCNF, LOC105371050 | GRCh38.p7 | 16:2456617 | ATTGCTGCCAGGAAT[C/T]CAGTGATGAGGAGGC | 899 |
rs201097939 | in-del | -/CTAG | | | intron-variant, upstream-variant-2KB | CCNF, MIR6767 | GRCh38.p7 | 16:2444512 | CATCGTATTAGCCAG[-/CTAG]GATGGTCTCAATCTC | 899 |
rs201108509 | snp | C/G | 0.000209486 | 0.0102323 | intron-variant | CCNF | GRCh38.p7 | 16:2437123 | CTGTCCTGTCTGTCC[C/G]CGCAGTGTCTGTGTC | 899 |
rs201114363 | snp | C/T | 1.77492e-05 | 0.00297898 | missense | CCNF | GRCh38.p7 | 16:2455478 | GCCAGGAGGAGACGC[C/T]GCTGGGCAGCTTCCT | 899 |
rs201180045 | snp | G/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2447990 | AGCAGCCAAGGGACT[G/T]GGCCTCAGTCCAAGG | 899 |
rs201271212 | snp | A/G/T | 0.000350987 | 0.0132431 | missense | CCNF | GRCh38.p7 | 16:2449456 | GCCAGACTGACGCAC[A/G/T]GGCAGAGTAAGGAGT | 899 |
rs201290179 | snp | C/T | 4.96389e-05 | 0.00498166 | missense | CCNF | GRCh38.p7 | 16:2453224 | GCTTCCATGATGACG[C/T]CCCCAAGGACTACAG | 899 |
rs201347478 | in-del | -/A | 0.0197687 | 0.0974348 | intron-variant | CCNF | GRCh38.p7 | 16:2453778 | CTCTGACTGGGCTCC[-/A]CTGTGGAGGAAGATG | 899 |
rs201361389 | snp | C/T | 4.94662e-05 | 0.00497299 | synonymous-codon | CCNF | GRCh38.p7 | 16:2448945 | GGTGAGAATGATGGG[C/T]GAGATCGTCTCCGCC | 899 |
rs201372661 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, synonymous-codon | CCNF | GRCh38.p7 | 16:2439790 | CAGCTTCCGAAAACT[C/G]AGGGACTACGCTGCC | 899 |
rs201460257 | snp | C/T | 0.00010006 | 0.00707248 | missense, downstream-variant-500B | CCNF, LOC105371050 | GRCh38.p7 | 16:2456752 | CAGGGAAGGACGTCA[C/T]GACCTCAGGGTACTC | 899 |
rs201540325 | snp | G/T | 0.0139422 | 0.0823209 | missense, downstream-variant-500B | CCNF, MIR6767 | GRCh38.p7 | 16:2445481 | TGATCGACTGGCTGG[G/T]GGAAGTTGCCACCAT | 899 |
rs201655281 | in-del | -/C | | | intron-variant | CCNF | GRCh38.p7 | 16:2437010 | TACTCTCCTGAAACA[-/C]CAGCTGCTTTGCACT | 899 |
rs201692958 | snp | C/G/T | 0.000232043 | 0.010769 | intron-variant | CCNF | GRCh38.p7 | 16:2453546 | CCAAACGGTTAGTTA[C/G/T]CCTGCGTTCTGGCTG | 899 |
rs201721282 | snp | C/G/T | 0.000408214 | 0.0142809 | intron-variant | CCNF | GRCh38.p7 | 16:2439726 | CACAGTTGTACAAAG[C/G/T]CTCGGTGATCTCCCA | 899 |
rs201788118 | snp | A/G | 6.9062e-05 | 0.0058759 | missense | CCNF | GRCh38.p7 | 16:2449441 | GCAGCCCTGCTCCTG[A/G]CCAGACTGACGCACG | 899 |
rs201795637 | snp | A/C | | | intron-variant | CCNF | GRCh38.p7 | 16:2436263 | AGAGTTCAGCGTGCC[A/C]TGTAACACAGAGCCA | 899 |
rs201813739 | snp | C/G/T | 4.94224e-05 | 0.00497083 | utr-variant-5-prime, missense, synonymous-codon, upstream-variant-2KB | CCNF, MIR6767 | GRCh38.p7 | 16:2443717 | AGCTTCCAGTGAGAT[C/G/T]GTCTGCCAGCTATTT | 899 |
rs201815006 | snp | A/G | 0.000383829 | 0.013848 | intron-variant, upstream-variant-2KB | CCNF, MIR6767 | GRCh38.p7 | 16:2443835 | GCTTCTAATCAGAGC[A/G]GCGCGGAAGCCAGCC | 899 |
rs201858204 | snp | A/G | 1.65765e-05 | 0.00287888 | intron-variant, upstream-variant-2KB | CCNF, MIR6767 | GRCh38.p7 | 16:2443817 | TGAGGCATTCAGGCC[A/G]GGGCTTCTAATCAGA | 899 |
rs201977657 | snp | A/C | 0.0191251 | 0.0958999 | missense, downstream-variant-500B | CCNF, MIR6767 | GRCh38.p7 | 16:2445508 | CCATGAAGGACTTCA[A/C]AAGCCTGTGCCTGCA | 899 |
rs201996443 | snp | C/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2435682 | ATATATATATATATA[C/T]ATATATATATATATA | 899 |
rs202050678 | snp | A/G | 0.000115763 | 0.0076071 | utr-variant-5-prime, missense | CCNF | GRCh38.p7 | 16:2437209 | GCTGAGCGGCTGAAT[A/G]TGGGTGCCGCACCTT | 899 |
rs202212196 | in-del | -/TGTGG | 0.0197687 | 0.0974348 | intron-variant | CCNF | GRCh38.p7 | 16:2453780 | TCTGACTGGGCTCCC[-/TGTGG]AGGAAGATGGTTTCG | 899 |
rs202217366 | snp | G/T | 0.000302084 | 0.0122862 | intron-variant | CCNF | GRCh38.p7 | 16:2449809 | ATCCCCTCCACCCCT[G/T]GCCTGCTTTCCTCCC | 899 |
rs367545509 | snp | A/G | | | intron-variant, downstream-variant-500B | CCNF | GRCh38.p7 | 16:2447640 | CCTGTAGTCCCATCT[A/G]CTTGGGAGGCTGAGG | 899 |
rs367591984 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | CCNF | GRCh38.p7 | 16:2431108 | TTCATCTTATCAAGG[C/T]TTCTGTCTTTTTTTC | 899 |
rs367642337 | snp | C/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2454343 | GGAGACCTGACCCTC[C/T]TGTGTCACTCCACAC | 899 |
rs367714569 | snp | A/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2442605 | ATATAATATTATATA[A/T]TATAATATTATATAT | 899 |
rs367823441 | snp | C/T | 0.00014832 | 0.00861035 | intron-variant | CCNF | GRCh38.p7 | 16:2438161 | CTGGGACTTTGTGTT[C/T]GATACATCCCTAGCC | 899 |
rs367856930 | snp | A/G/T | 3.32797e-05 | 0.00407908 | utr-variant-5-prime, synonymous-codon | CCNF | GRCh38.p7 | 16:2437169 | AGAAGTGAATGGCCT[A/G/T]AAGGCCTCTCGCTTC | 899 |
rs367906067 | snp | A/G | | | intron-variant, downstream-variant-500B, upstream-variant-2KB | CCNF, C16orf59, LOC105371050 | GRCh38.p7 | 16:2458959 | CCAGCTTGCACCTGA[A/G]GGAGGAAACCACTCC | 899 |
rs367911877 | snp | C/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2437775 | GTGGTGGTGCATACC[C/T]ATAGTCCCAGCTACT | 899 |
rs368003068 | snp | C/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2454311 | GCGTGACAGCACTTT[C/G]CATTGTGTGGAAGGC | 899 |
rs368016460 | in-del | -/A | | | intron-variant | CCNF | GRCh38.p7 | 16:2441084 | AAAAATACAAAAAAA[-/A]TTAGCTGGGCCTGGT | 899 |
rs368033051 | snp | A/G | 0.000128302 | 0.00800841 | utr-variant-3-prime, intron-variant | CCNF, LOC105371050 | GRCh38.p7 | 16:2457040 | GTCAGCACATTTGCC[A/G]CAGTGGATGTGTACT | 899 |
rs368055352 | snp | A/G | 0.000116297 | 0.00762464 | intron-variant | CCNF | GRCh38.p7 | 16:2453563 | CTGCGTTCTGGCTGC[A/G]CCATACAATGCTGGC | 899 |
rs368061011 | snp | A/C/T | 3.32696e-05 | 0.00407844 | intron-variant | CCNF | GRCh38.p7 | 16:2449014 | CCTTATTAATCTTCG[A/C/T]TGTCGCTGTGCTGGA | 899 |
rs368071746 | snp | G/T | 1.64743e-05 | 0.00287 | utr-variant-5-prime, missense, upstream-variant-2KB | CCNF, MIR6767 | GRCh38.p7 | 16:2443706 | CTGGAGGTGAGAGCT[G/T]CCAGTGAGATCGTCT | 899 |
rs368201621 | snp | A/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2451252 | GGCGCGGGCGGGGGC[A/G]ACTCCCTTCAGGGAG | 899 |
rs368324012 | snp | A/G | 1.66588e-05 | 0.00288602 | intron-variant | CCNF | GRCh38.p7 | 16:2453172 | AAAAATGGGGTGGGG[A/G]TGCCTCACATGTCCA | 899 |
rs368482479 | snp | C/T | 3.29902e-05 | 0.00406128 | synonymous-codon | CCNF | GRCh38.p7 | 16:2448957 | GGGCGAGATCGTCTC[C/T]GCCTTGGAAGGGAAG | 899 |
rs368492122 | in-del | -/TGTG | 0.0023933 | 0.0345097 | intron-variant | CCNF | GRCh38.p7 | 16:2438812 | GACCAACCTGGCCAA[-/TGTG]TTGAAACCACGTCTT | 899 |
rs368589562 | snp | G/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2454930 | CTGGGTGTGATGGCG[G/T]GCACCTGTAGTCCCA | 899 |
rs368592695 | snp | A/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2452618 | CACACAGTTGTGCTT[A/G]TCATCACAACAATCA | 899 |
rs368742607 | in-del | -/CACACA | | | intron-variant | CCNF | GRCh38.p7 | 16:2435637 | ACACACATATATATG[-/CACACA]CACACACATATATAT | 899 |
rs368783935 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CCNF | GRCh38.p7 | 16:2435476 | TGTAGTCCTAGCTAC[G/T]TGGGATGCCGGGGTG | 899 |
rs368809136 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2450242 | TGGTGGCTCACACCT[A/G]TAATCCCAGCACTTT | 899 |
rs368874011 | snp | C/T | 0.000164764 | 0.00907495 | intron-variant | CCNF | GRCh38.p7 | 16:2449923 | AAGAAGTGGTGAGTT[C/T]TGGCCGGGCGCAGAG | 899 |
rs368886262 | snp | A/C/G | 8.28639e-05 | 0.00643633 | intron-variant | CCNF | GRCh38.p7 | 16:2453351 | CTCATGGGGTGCTGG[A/C/G]GTGTGGGCGGGCCTC | 899 |
rs368889723 | snp | A/G | 5.01962e-05 | 0.00500955 | intron-variant, nc-transcript-variant | CCNF, MIR6767 | GRCh38.p7 | 16:2445440 | CCCACCAGTTCCCAC[A/G]TGCTTCTCTTTCCGC | 899 |
rs369041340 | snp | A/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2436099 | CCTCTTGTTTTAGCA[A/G]ACCCTTTAATTTCAG | 899 |
rs369103056 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | CCNF | GRCh38.p7 | 16:2440488 | TGGGCGTGGTGGCAG[C/G]CACCTGATACTCAGG | 899 |
rs369116649 | snp | C/T | 6.69691e-05 | 0.0057862 | missense, downstream-variant-500B | CCNF, LOC105371050 | GRCh38.p7 | 16:2456674 | ACCCACAGGCACTGG[C/T]GCTGGACACCCAGAT | 899 |
rs369118022 | snp | C/T | | | synonymous-codon, nc-transcript-variant | CCNF, LOC105371050 | GRCh38.p7 | 16:2456942 | GGAGAGCAGTGTTCC[C/T]CAGCAACAGGTGAAG | 899 |
rs369144402 | snp | A/G | 7.06015e-05 | 0.00594102 | missense | CCNF | GRCh38.p7 | 16:2449462 | CTGACGCACGGGCAG[A/G]GTAAGGAGTGGCCCT | 899 |
rs369236896 | snp | A/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2449814 | CTCCACCCCTGGCCT[A/G]CTTTCCTCCCCAGCA | 899 |
rs369245530 | snp | C/G | 3.61422e-05 | 0.00425086 | intron-variant, missense | CCNF | GRCh38.p7 | 16:2432994 | GACCTGGTGGACAAC[C/G]ACGCCAGTGTGTGGG | 899 |
rs369290461 | snp | A/G | 3.40449e-05 | 0.00412568 | intron-variant | CCNF | GRCh38.p7 | 16:2430989 | TGGGACAAGAAGCAT[A/G]GTTCCATCTTTTGTG | 899 |
rs369296450 | snp | A/G/T | 0.00011566 | 0.00760381 | missense | CCNF | GRCh38.p7 | 16:2453259 | GTCTCTCTGACCGCC[A/G/T]TGAAGCAGCGGTTTG | 899 |
rs369391906 | snp | A/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2433900 | AAATCCAGATCGACA[A/G]CCAACCAGGGCAGGC | 899 |
rs369514974 | snp | C/T | 3.21053e-05 | 0.00400645 | intron-variant | CCNF | GRCh38.p7 | 16:2439494 | TCGGGGGGAGTTATG[C/T]TGGACAAAGGCGTAG | 899 |
rs369575128 | snp | A/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2431335 | ATTGTTGATTATACC[A/T]TCAGGCCTTGTGTTC | 899 |
rs369608868 | snp | C/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2435244 | CAACAGAGCAGACTC[C/T]GTCTCAAAAAAAAAA | 899 |
rs369719151 | snp | C/T | 3.34068e-05 | 0.00408684 | synonymous-codon, downstream-variant-500B | CCNF, LOC105371050 | GRCh38.p7 | 16:2456726 | ACCCCTGGTCCGCAC[C/T]AGCCGGGAGCCAGGG | 899 |
rs369725393 | snp | A/G | 1.65048e-05 | 0.00287265 | utr-variant-5-prime, missense, upstream-variant-2KB | CCNF, MIR6767 | GRCh38.p7 | 16:2443790 | CAGAAGGGACTCAAT[A/G]ACACAATGAGGTGAG | 899 |
rs369730776 | snp | A/G | 0.000138284 | 0.00831401 | missense | CCNF | GRCh38.p7 | 16:2455400 | CACCTTGCAGGAAGC[A/G]GGAGAACAGCCTCCA | 899 |
rs369771851 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | CCNF, MIR6767 | GRCh38.p7 | 16:2445218 | TCGAGGTCTCAAAGC[A/G]CTTGTGTTTGGGAGC | 899 |
rs369819157 | snp | A/G | 0.000205458 | 0.0101335 | intron-variant | CCNF | GRCh38.p7 | 16:2439316 | TAAAAATGAAAAAGA[A/G]TAAGGGAACAATGAA | 899 |
rs369890297 | snp | C/T | 0.000595356 | 0.0172431 | synonymous-codon | CCNF | GRCh38.p7 | 16:2453225 | CTTCCATGATGACGC[C/T]CCCAAGGACTACAGG | 899 |
rs369932788 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | CCNF | GRCh38.p7 | 16:2449796 | CTCCGTCCCCTCCAT[C/T]CCCTCCACCCCTGGC | 899 |
rs369973675 | snp | A/G | 0.000153988 | 0.00877328 | missense | CCNF | GRCh38.p7 | 16:2453416 | TCCCCTCAGGTGCTG[A/G]GCTACAGCCAGTTGT | 899 |
rs369985302 | snp | A/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2449607 | CTCCTACCTTCAGTG[A/G]TGTCCCAGATTTCTG | 899 |
rs370036552 | snp | C/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2432798 | GCTCTTTTATCTGCT[C/T]AAAGTGACAGTTACT | 899 |
rs370108585 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | CCNF | GRCh38.p7 | 16:2451055 | TGGTGAGCCTGGCCC[C/G]GCCCTCGCCACATCT | 899 |
rs370117441 | snp | A/G | 0.000153988 | 0.00877328 | missense | CCNF | GRCh38.p7 | 16:2453509 | ATCCACGCCTTCCTC[A/G]GCTCTCCCTCGGGGC | 899 |
rs370124813 | snp | A/G | 1.66796e-05 | 0.00288782 | intron-variant | CCNF | GRCh38.p7 | 16:2449276 | CACCCCGTCCCGGCT[A/G]TCTAGGTCCCCACTG | 899 |
rs370154810 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2437785 | ATACCTATAGTCCCA[A/G]CTACTCAGGAGGCTG | 899 |
rs370263039 | snp | A/G | 3.31906e-05 | 0.0040736 | intron-variant | CCNF | GRCh38.p7 | 16:2453552 | GGTTAGTTACCCTGC[A/G]TTCTGGCTGCGCCAT | 899 |
rs370297503 | snp | A/G | 1.66538e-05 | 0.00288559 | synonymous-codon, downstream-variant-500B | CCNF, LOC105371050 | GRCh38.p7 | 16:2456762 | CGTCACGACCTCAGG[A/G]TACTCCTCCGTCAGC | 899 |
rs370340261 | snp | A/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2435048 | TCATGAGATCAGATC[A/G]AGACCATCCTGGCTA | 899 |
rs370349434 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | CCNF | GRCh38.p7 | 16:2437092 | ACATTCCGTCCCTAA[A/G]AGACATCCCTGGGCT | 899 |
rs370404418 | snp | C/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2451061 | GCCTGGCCCGGCCCT[C/T]GCCACATCTAAGCCC | 899 |
rs370448527 | snp | C/T | 0.000182275 | 0.00954485 | missense, nc-transcript-variant | CCNF, LOC105371050 | GRCh38.p7 | 16:2456926 | GTCCCCCAAGTCCCC[C/T]GGAGAGCAGTGTTCC | 899 |
rs370544708 | snp | A/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2438427 | TCGTGGGCCTCTCCT[A/G]CTCGTGTGGACCTCT | 899 |
rs370555054 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CCNF | GRCh38.p7 | 16:2454332 | TGTGGAAGGCAGGAG[A/G]CCTGACCCTCCTGTG | 899 |
rs370623539 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | CCNF, MIR6767 | GRCh38.p7 | 16:2444552 | TGATCCGCCTGCCTC[C/T]GCCTCCCAAAGTGCT | 899 |
rs370702853 | snp | A/C/G | 3.304e-05 | 0.00406437 | splice-donor-variant | CCNF | GRCh38.p7 | 16:2435874 | TCTACAATGAAGGCC[A/C/G]TAAGTCCTCACCCCA | 899 |
rs370713307 | snp | A/G | 0.000166981 | 0.00913579 | intron-variant | CCNF | GRCh38.p7 | 16:2449267 | GAGAGCCCACACCCC[A/G]TCCCGGCTGTCTAGG | 899 |
rs370765591 | snp | A/G | 0.000571755 | 0.0168982 | intron-variant | CCNF | GRCh38.p7 | 16:2455609 | GGACATCACACAGAG[A/G]GTGGCTCTCACCGAG | 899 |
rs370903607 | snp | C/T | 3.29625e-05 | 0.00405958 | intron-variant | CCNF | GRCh38.p7 | 16:2438134 | TCGAGGTGAGTCAAG[C/T]TGTTCTCTGCACTGG | 899 |
rs371006053 | snp | C/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2434186 | TGATGGGCACTTGTA[C/G]TCCCAGCTACTCTGG | 899 |
rs371013033 | snp | A/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2453892 | CTGCTGTCACTCCCG[A/G]CACTCGAGCTGTGAC | 899 |
rs371050277 | snp | A/G | 0.000132192 | 0.00812887 | missense, downstream-variant-500B | CCNF, MIR6767 | GRCh38.p7 | 16:2445559 | ACCGGTACCTGCGGA[A/G]GAGGCTGGTGCCGCG | 899 |
rs371078328 | snp | C/T | 0.000307953 | 0.0124049 | intron-variant, upstream-variant-2KB | CCNF, MIR6767 | GRCh38.p7 | 16:2443600 | TTCAGAAATGGAAAA[C/T]TGCAACATGGCTGCT | 899 |
rs371121254 | snp | C/T | 1.64836e-05 | 0.0028708 | synonymous-codon | CCNF | GRCh38.p7 | 16:2448891 | GACCATCCGGGAGGC[C/T]GTATGGCTCACGGAC | 899 |
rs371188956 | snp | C/T | 0.000582165 | 0.0170512 | intron-variant | CCNF | GRCh38.p7 | 16:2437334 | GAGGGTGAGTCTGGG[C/T]GAGGGGCAGCACCTG | 899 |
rs371204156 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | CCNF | GRCh38.p7 | 16:2450913 | GGATAGAGCTATCCT[C/T]TGTCTCACTGAGAAG | 899 |
rs371285950 | snp | C/T | 0.000149233 | 0.00863679 | intron-variant | CCNF | GRCh38.p7 | 16:2453359 | GTGCTGGGGTGTGGG[C/T]GGGCCTCACCCTCGG | 899 |
rs371389975 | snp | A/G/T | 8.2401e-05 | 0.00641833 | intron-variant | CCNF | GRCh38.p7 | 16:2438162 | TGGGACTTTGTGTTC[A/G/T]ATACATCCCTAGCCG | 899 |
rs371391701 | snp | C/T | 0.000109739 | 0.00740659 | utr-variant-3-prime, intron-variant | CCNF, LOC105371050 | GRCh38.p7 | 16:2457070 | TGAGGGGGCTGGAGG[C/T]GAAGGGTGGGAGCAT | 899 |
rs371399576 | snp | A/G | 0.00375418 | 0.0431625 | intron-variant | CCNF | GRCh38.p7 | 16:2439506 | ATGCTGGACAAAGGC[A/G]TAGTTGATGCTGGTC | 899 |
rs371593737 | snp | C/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2456139 | GCACTGTAGCCTGGG[C/T]GTTCTTTCTAGAATG | 899 |
rs371599778 | snp | A/C | | | intron-variant | CCNF | GRCh38.p7 | 16:2449214 | AGACCCTGCGCTGGG[A/C]CTGCATGCGGCACTG | 899 |
rs371643212 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | CCNF | GRCh38.p7 | 16:2439570 | GCTCTTGCTGCTCCC[A/G]GTCTCTCAGCCTCCG | 899 |
rs371687851 | snp | A/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2431884 | CACCCAGGCTGGAGT[A/G]CAGTAGCGCAATCTC | 899 |
rs371699142 | snp | A/G | 8.4791e-05 | 0.00651063 | utr-variant-5-prime, missense | CCNF | GRCh38.p7 | 16:2437150 | TGTCTGATGAGGCCC[A/G]CGCAGAAGTGAATGG | 899 |
rs371783851 | snp | A/G | 8.26713e-05 | 0.00642875 | utr-variant-5-prime, missense | CCNF | GRCh38.p7 | 16:2437201 | TCAGTCTCGCTGAGC[A/G]GCTGAATGTGGGTGC | 899 |
rs371813732 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CCNF | GRCh38.p7 | 16:2429722 | TCGGAGCCTTCCCCC[A/G]CGGCGACGTTTTCCG | 899 |
rs371876390 | snp | A/G | 0.000185403 | 0.00962639 | intron-variant | CCNF | GRCh38.p7 | 16:2437335 | AGGGTGAGTCTGGGC[A/G]AGGGGCAGCACCTGC | 899 |
rs371901886 | snp | C/G/T | 4.94184e-05 | 0.00497063 | utr-variant-5-prime, missense, stop-gained | CCNF | GRCh38.p7 | 16:2431195 | ATAAGGAGGAGGCCC[C/G/T]GAAACCTGACCATCT | 899 |
rs371914315 | snp | G/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2435222 | CGCCACTGCACTCCA[G/T]CCTGGGCAACAGAGC | 899 |
rs371917368 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CCNF | GRCh38.p7 | 16:2451583 | TTTTTCCTTTTTTGA[A/G]TTGGGGGCCCAGGCT | 899 |
rs372004931 | snp | C/T | 0.000248973 | 0.0111546 | intron-variant | CCNF | GRCh38.p7 | 16:2453186 | GGTGCCTCACATGTC[C/T]ACTCCACGTGACTCT | 899 |
rs372100662 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | CCNF | GRCh38.p7 | 16:2454734 | TGCAATCTGCCTGGC[A/G]CCGGGCTAAGCACTG | 899 |
rs372168494 | snp | A/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2455108 | TGGCATCATCCTAGA[A/G]GTTTCCAGGGGACCA | 899 |
rs372292640 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2438698 | GTAGAGTGATTGAAC[A/G]TCAAGTAAAGAATAA | 899 |
rs372430287 | snp | A/G | 1.65392e-05 | 0.00287564 | intron-variant | CCNF | GRCh38.p7 | 16:2449007 | CCATTTTCCTTATTA[A/G]TCTTCGTTGTCGCTG | 899 |
rs372434396 | snp | C/G | 0.000229974 | 0.0107207 | utr-variant-5-prime, intron-variant | CCNF | GRCh38.p7 | 16:2429472 | CGGCGGCAGCGACGC[C/G]AGCGCGGCGATGGGG | 899 |
rs372474233 | snp | A/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2441593 | GGCTAGAGCACAGTG[A/G]TGCGATCTCAGCTCA | 899 |
rs372530306 | snp | A/G | | | upstream-variant-2KB, intron-variant | CCNF | GRCh38.p7 | 16:2429151 | GGGAAGCGCTCCTAC[A/G]GGACCCCAGCCCCGT | 899 |
rs372531268 | snp | C/T | 0.000308259 | 0.0124111 | intron-variant, downstream-variant-500B | CCNF, MIR6767 | GRCh38.p7 | 16:2445655 | CCCAGCTGGCAGGGA[C/T]GTGCTGGCCTTTCCC | 899 |
rs372548792 | snp | C/T | 0.000960217 | 0.0218903 | intron-variant | CCNF | GRCh38.p7 | 16:2453333 | CTCCCGCCACCTGGG[C/T]GTCTCATGGGGTGCT | 899 |
rs372591776 | snp | A/C | | | intron-variant | CCNF | GRCh38.p7 | 16:2449699 | CCCTGAGCTCCAAGA[A/C]ACTCCACAGCAGAGC | 899 |
rs372723774 | snp | G/T | 0.000562541 | 0.0167617 | missense | CCNF | GRCh38.p7 | 16:2453414 | CTTCCCCTCAGGTGC[G/T]GAGCTACAGCCAGTT | 899 |
rs372808586 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | CCNF | GRCh38.p7 | 16:2435303 | TGTTCTAGAGCCGGG[C/T]ATGATGGCTCAAGCC | 899 |
rs372892772 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | CCNF, MIR6767 | GRCh38.p7 | 16:2443958 | GGAGTCTCGCTCTGT[C/T]GCCCAGGCTGGAGTG | 899 |
rs372916893 | snp | A/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2442606 | TATAATATTATATAA[A/T]ATAATATTATATATA | 899 |
rs373001781 | snp | C/T | 1.89662e-05 | 0.0030794 | synonymous-codon, downstream-variant-500B | CCNF, LOC105371050 | GRCh38.p7 | 16:2456564 | AGCTCCCAGCGGCAT[C/T]CTCGATGTCACCGTG | 899 |
rs373108191 | snp | A/C | | | intron-variant | CCNF | GRCh38.p7 | 16:2452352 | GCTGCTTTCTCCTGC[A/C]GTGCCCGGACCCTGT | 899 |
rs373269867 | snp | C/T | 6.91934e-05 | 0.00588149 | intron-variant, nc-transcript-variant | CCNF, MIR6767 | GRCh38.p7 | 16:2445421 | GGGACACATGGAGAA[C/T]GCCCCCACCAGTTCC | 899 |
rs373272884 | snp | A/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2452830 | GGTGATTTCCCTCGC[A/G]GTAACGTTTGCTGGG | 899 |
rs373302631 | snp | C/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2456051 | CTGTGGTCCCAGCTA[C/T]TCAGGAGGCTGAGGT | 899 |
rs373303237 | in-del | -/C | 0.00119737 | 0.0244387 | intron-variant | CCNF | GRCh38.p7 | 16:2454553 | GGATAGCTCTCTCCA[-/C]CCCCCGCCCTCCACC | 899 |
rs373388890 | snp | C/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2449823 | TGGCCTGCTTTCCTC[C/G]CCAGCACAGCCCTGG | 899 |
rs373412669 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2449798 | CCGTCCCCTCCATCC[C/T]CTCCACCCCTGGCCT | 899 |
rs373559092 | snp | C/T | 8.31857e-05 | 0.00644871 | intron-variant, nc-transcript-variant | CCNF, MIR6767 | GRCh38.p7 | 16:2445450 | CCCACGTGCTTCTCT[C/T]TCCGCAGGTACATTC | 899 |
rs373727270 | snp | C/T | 0.000648449 | 0.0179946 | synonymous-codon, downstream-variant-500B | CCNF, LOC105371050 | GRCh38.p7 | 16:2456771 | CTCAGGGTACTCCTC[C/T]GTCAGCACCGCAAGT | 899 |
rs373734213 | snp | A/G | 1.65031e-05 | 0.00287251 | utr-variant-5-prime, missense, upstream-variant-2KB | CCNF, MIR6767 | GRCh38.p7 | 16:2443788 | TGCAGAAGGGACTCA[A/G]TGACACAATGAGGTG | 899 |
rs373805200 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | CCNF | GRCh38.p7 | 16:2450397 | GCGCCTGCAATCCCA[C/G]CTACTCAGGAGGCTG | 899 |
rs373826341 | snp | A/G | | | utr-variant-3-prime, intron-variant | CCNF, LOC105371050 | GRCh38.p7 | 16:2457508 | CCCCTCATCCACCTC[A/G]GCCTGCATGGGGCAC | 899 |
rs373827778 | snp | C/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2430413 | GAGGAGAGAGCACAT[C/T]TGAGAAGCATGTCCG | 899 |
rs373833071 | snp | C/T | 4.9657e-05 | 0.00498257 | intron-variant | CCNF | GRCh38.p7 | 16:2448836 | GGCTCCACCCTGAGA[C/T]CCCTTCTCGGCGTTG | 899 |
rs373857853 | snp | C/T | 1.66899e-05 | 0.00288871 | synonymous-codon, downstream-variant-500B | CCNF, LOC105371050 | GRCh38.p7 | 16:2456747 | GGAGCCAGGGAAGGA[C/T]GTCACGACCTCAGGG | 899 |
rs373859621 | snp | A/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2440646 | GCTCCTATTTGCCAA[A/G]TGGATAGAAGCTTGT | 899 |
rs373865670 | snp | A/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2437826 | ATCGCTTGAGCCTGG[A/G]AGGTTGAGCTTGCAA | 899 |
rs373869359 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2454200 | GGCTGCCTCCAGAAG[C/T]GTTGTGTCGGGAGTG | 899 |
rs373872375 | snp | A/G | 0.000110544 | 0.00743369 | missense, downstream-variant-500B | CCNF, LOC105371050 | GRCh38.p7 | 16:2456577 | ATCCTCGATGTCACC[A/G]TGGTCTACCTGAACC | 899 |
rs373873685 | snp | A/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2433912 | ACAGCCAACCAGGGC[A/T]GGCAGCCATGTTGCC | 899 |
rs373935407 | snp | C/G/T | 5.13539e-05 | 0.00506703 | synonymous-codon | CCNF | GRCh38.p7 | 16:2449425 | AGCCCGCCTGGCTGC[C/G/T]GCAGCCCTGCTCCTG | 899 |
rs373963885 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | CCNF | GRCh38.p7 | 16:2453925 | GAGTCACATCCCCAG[C/G]ACTTCCCTCGCCACC | 899 |
rs373992181 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CCNF | GRCh38.p7 | 16:2450957 | GTGGGTCCCTTGCGC[C/T]GTCGTGCCCGGATGT | 899 |
rs374015103 | in-del | -/TCCCCCCCA/TCCCCTCCA/TCCCCTCCATCCCCTCCA/TCCCCTCCATCCCCTCCATCCCCTCCA/TCCCCTCCATCCCCTCCGTCCCCTCCA | 0.404272 | 0.196814 | intron-variant | CCNF | GRCh38.p7 | 16:2449785 | CCTCCATCCCCTCCG[lengthTooLong]TCCCCTCCATCCCCT | 899 |
rs374039070 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | CCNF | GRCh38.p7 | 16:2451246 | GCAGGTGGCGCGGGC[A/G]GGGGCGACTCCCTTC | 899 |
rs374043839 | snp | C/G | 2.62954e-05 | 0.00362588 | utr-variant-3-prime, intron-variant | CCNF, LOC105371050 | GRCh38.p7 | 16:2457045 | CACATTTGCCGCAGT[C/G]GATGTGTACTGAGGG | 899 |
rs374100567 | snp | A/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2453799 | GAGGAAGATGGTTTC[A/G]AGCACGCGGGAGCCT | 899 |
rs374118703 | snp | A/G | 1.70697e-05 | 0.00292139 | missense, nc-transcript-variant | CCNF, LOC105371050 | GRCh38.p7 | 16:2456959 | AGCAACAGGTGAAGC[A/G]GATAAACCTATGCAT | 899 |
rs374120930 | snp | C/T | 6.6096e-05 | 0.00574836 | missense | CCNF | GRCh38.p7 | 16:2453283 | CGGTTTGAGGACAAG[C/T]GCTATGGAGAAATCA | 899 |
rs374133804 | snp | A/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2442601 | TAATATATAATATTA[A/T]ATAATATAATATTAT | 899 |
rs374224977 | snp | C/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2438474 | GTGAAACCACGTCTT[C/T]ACTAAAAAACACAAA | 899 |
rs374228248 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CCNF | GRCh38.p7 | 16:2454711 | CCGCCCAAGGCCAGG[C/T]CATTCCATGCAATCT | 899 |
rs374295127 | snp | G/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2439846 | GGTGCGGGGCTGGGA[G/T]GACGTGGGGAGCTGG | 899 |
rs374319260 | snp | A/C/G | 0.000208819 | 0.0102162 | intron-variant | CCNF | GRCh38.p7 | 16:2437125 | GTCCTGTCTGTCCCC[A/C/G]CAGTGTCTGTGTCTG | 899 |
rs374324488 | snp | C/T | 1.64811e-05 | 0.00287059 | intron-variant | CCNF | GRCh38.p7 | 16:2438144 | TCAAGTTGTTCTCTG[C/T]ACTGGGACTTTGTGT | 899 |
rs374347098 | snp | C/T | 0.000251935 | 0.0112207 | intron-variant | CCNF | GRCh38.p7 | 16:2439480 | GTGCCTGCTCTGGGT[C/T]GGGGGGAGTTATGCT | 899 |
rs374485469 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant, upstream-variant-2KB | CCNF, MIR6767 | GRCh38.p7 | 16:2443602 | CAGAAATGGAAAACT[A/G]CAACATGGCTGCTGT | 899 |
rs374486523 | snp | C/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2447871 | CCACTGACATCTTGT[C/G]TTTTTGGCGTCTGCA | 899 |
rs374561010 | snp | C/G | 0.000149023 | 0.00863071 | intron-variant | CCNF | GRCh38.p7 | 16:2453399 | ACCCCCTAACTCTAG[C/G]TTCCCCTCAGGTGCT | 899 |
rs374687701 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CCNF, MIR6767 | GRCh38.p7 | 16:2444493 | TTTTAGTAGAGATGG[C/G]GTTTCATCGTATTAG | 899 |
rs374735211 | snp | C/G | | | intron-variant, upstream-variant-2KB | CCNF, MIR6767 | GRCh38.p7 | 16:2443983 | GGAGTGCAGTGGCGC[C/G]ATCTCAGCTCACTGC | 899 |
rs374738398 | snp | C/T | 5.27005e-05 | 0.00513298 | intron-variant | CCNF | GRCh38.p7 | 16:2437117 | TGGGCTCTGTCCTGT[C/T]TGTCCCCGCAGTGTC | 899 |
rs374785734 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | CCNF | GRCh38.p7 | 16:2449016 | TTATTAATCTTCGTT[A/G]TCGCTGTGCTGGAGG | 899 |
rs374851448 | snp | C/T | 1.65285e-05 | 0.00287471 | synonymous-codon | CCNF | GRCh38.p7 | 16:2453255 | GCAAGTCTCTCTGAC[C/T]GCCGTGAAGCAGCGG | 899 |
rs374972864 | in-del | -/TATATATATA | | | intron-variant | CCNF | GRCh38.p7 | 16:2441938 | ATGATATTAGCAAAT[-/TATATATATA]TATATATATATATAT | 899 |
rs374999333 | snp | C/G/T | 5.71363e-05 | 0.00534461 | intron-variant | CCNF | GRCh38.p7 | 16:2433098 | GAGAATGGCTCAGTC[C/G/T]TCTCCTGCCTTGGCC | 899 |
rs375048974 | snp | A/G | 0.000153988 | 0.00877328 | utr-variant-5-prime, synonymous-codon | CCNF | GRCh38.p7 | 16:2431260 | GAAATGGCTTTCTGT[A/G]GAGGACATCCTGGCC | 899 |
rs375100764 | snp | A/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2430987 | TTTGGGACAAGAAGC[A/G]TAGTTCCATCTTTTG | 899 |
rs375114742 | snp | C/T | | | upstream-variant-2KB, intron-variant | CCNF | GRCh38.p7 | 16:2428913 | GAGCGACCCCGGGAC[C/T]CGGGCAGGGCACGGC | 899 |
rs375251632 | snp | A/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2435246 | ACAGAGCAGACTCCG[A/T]CTCAAAAAAAAAAAA | 899 |
rs375260823 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | CCNF, MIR6767 | GRCh38.p7 | 16:2444170 | GTGATCCGCCCGCTT[C/T]GGCCTCCCAAAGTGC | 899 |
rs375261111 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CCNF | GRCh38.p7 | 16:2438176 | CGATACATCCCTAGC[C/T]GAGATCCTGGAACTG | 899 |
rs375320785 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CCNF | GRCh38.p7 | 16:2437545 | TTCTGGGTACACGTG[C/T]TGACAGCTGGAAACA | 899 |
rs375380091 | snp | A/C | | | intron-variant | CCNF | GRCh38.p7 | 16:2443373 | ACTTAACACAGCTTC[A/C]CCAGGCATTAGCCAT | 899 |
rs375454117 | snp | C/T | 0.000148328 | 0.00861056 | intron-variant | CCNF | GRCh38.p7 | 16:2431111 | ATCTTATCAAGGCTT[C/T]TGTCTTTTTTTCCTT | 899 |
rs375467600 | snp | C/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2448607 | TTTGAAGAGATAGGG[C/T]CTTGCTTTGTTGCCC | 899 |
rs375501461 | snp | A/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2438300 | CTGGCCACGGGCTCC[A/G]ATCCTGGCTCCATGA | 899 |
rs375523895 | snp | C/G | 1.64781e-05 | 0.00287033 | missense | CCNF | GRCh38.p7 | 16:2449838 | CCCAGCACAGCCCTG[C/G]ACCACTCAGCTGTGG | 899 |
rs375714600 | snp | A/T | 2.24772e-05 | 0.00335233 | utr-variant-5-prime, missense | CCNF | GRCh38.p7 | 16:2439402 | TTGAGGAGGCTGCTC[A/T]TCAGGGATGTCTGAC | 899 |
rs375754971 | snp | C/T | 0.000153988 | 0.00877328 | synonymous-codon | CCNF | GRCh38.p7 | 16:2453436 | CAGCCAGTTGTGTGC[C/T]GCATTAGGAGTGACA | 899 |
rs375755671 | snp | A/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2441726 | TTCACCATGTTGGCC[A/T]GGCTGGTCTAAAACT | 899 |
rs376056912 | snp | C/G | 1.68275e-05 | 0.0029006 | utr-variant-5-prime, missense | CCNF | GRCh38.p7 | 16:2437155 | GATGAGGCCCGCGCA[C/G]AAGTGAATGGCCTGA | 899 |
rs376090217 | snp | C/G/T | 0.00358779 | 0.0422022 | intron-variant | CCNF | GRCh38.p7 | 16:2437470 | TGCAGATATGGGGAA[C/G/T]GCATCTGGAAATCAG | 899 |
rs376142462 | snp | A/G | 3.18588e-05 | 0.00399104 | intron-variant | CCNF | GRCh38.p7 | 16:2437349 | CGAGGGGCAGCACCT[A/G]CGAGGCCACCTGCAG | 899 |
rs376192800 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CCNF | GRCh38.p7 | 16:2429328 | GGGGCCGGCGGCGGC[A/C]CCCCCGGGCAGGCCA | 899 |
rs376206216 | snp | A/G | 1.6666e-05 | 0.00288664 | intron-variant | CCNF | GRCh38.p7 | 16:2453171 | TAAAAATGGGGTGGG[A/G]GTGCCTCACATGTCC | 899 |
rs376214130 | in-del | -/TG | | | intron-variant, upstream-variant-2KB | CCNF, MIR6767 | GRCh38.p7 | 16:2443398 | AGCCATGTAAGAAAC[-/TG]AGACCTGAGCCACGG | 899 |
rs376235797 | in-del | -/A | 0.0115144 | 0.0749975 | intron-variant | CCNF | GRCh38.p7 | 16:2431384 | CTTTGGCTAAAAAAG[-/A]GGTTGGGGCAGAGGC | 899 |
rs376261035 | snp | A/G/T | 0.000189247 | 0.00972574 | intron-variant, nc-transcript-variant | CCNF, MIR6767 | GRCh38.p7 | 16:2445422 | GGACACATGGAGAAC[A/G/T]CCCCCACCAGTTCCC | 899 |
rs376290671 | snp | C/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2433866 | ATTCGCTGTGAGCCT[C/T]GTCCATCTGAGTTGC | 899 |
rs376294554 | snp | C/G/T | 3.31544e-05 | 0.0040714 | intron-variant, upstream-variant-2KB | CCNF, MIR6767 | GRCh38.p7 | 16:2443618 | CAACATGGCTGCTGT[C/G/T]TCACGCTCATGTTTG | 899 |
rs376297532 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | CCNF | GRCh38.p7 | 16:2436102 | CTTGTTTTAGCAAAC[C/G]CTTTAATTTCAGTTG | 899 |
rs376344984 | snp | C/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2441020 | GGGCGGATCACGAGG[C/T]CAAGAGGTCGAGACC | 899 |
rs376429792 | snp | C/T | 0.000166182 | 0.00911391 | intron-variant, nc-transcript-variant | CCNF, MIR6767 | GRCh38.p7 | 16:2445453 | ACGTGCTTCTCTTTC[C/T]GCAGGTACATTCTGA | 899 |
rs376455710 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2451028 | CTGCCCCGGCCCCTC[C/T]GCCCTTCTCTCTGGT | 899 |
rs376485139 | in-del | -/ATATATGTT | | | intron-variant | CCNF | GRCh38.p7 | 16:2443178 | TATAATATATATATA[-/ATATATGTT]ATATATAATATATAT | 899 |
rs376486180 | snp | A/G | 3.36802e-05 | 0.00410353 | utr-variant-5-prime, synonymous-codon | CCNF | GRCh38.p7 | 16:2439823 | AGGCTGCTGGGAAGC[A/G]CAGGTGAGGTGCGGG | 899 |
rs376492968 | snp | C/T | 4.60713e-05 | 0.00479932 | intron-variant | CCNF | GRCh38.p7 | 16:2455382 | GGTCTCCTGGGCTCT[C/T]TCCACCTTGCAGGAA | 899 |
rs376535750 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2452591 | GATTGTGTGATTTAA[C/T]GGGCTTTTATTCACA | 899 |
rs376574463 | snp | A/T | | | intron-variant, upstream-variant-2KB | CCNF, MIR6767 | GRCh38.p7 | 16:2445188 | CTGTGGGCTGACTTT[A/T]CACTTTGCGTCAGGT | 899 |
rs376665678 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CCNF | GRCh38.p7 | 16:2456235 | GTGCAAACCCCAGGC[A/G]GACTGCGGGGTCCTT | 899 |
rs376699320 | snp | C/T | 0.000153988 | 0.00877328 | utr-variant-5-prime, synonymous-codon | CCNF | GRCh38.p7 | 16:2435827 | TGAAAAGGGGAATTT[C/T]GAAGCTGCTGTGAAG | 899 |
rs376708449 | snp | A/G | 0.000117539 | 0.00766524 | intron-variant | CCNF | GRCh38.p7 | 16:2449245 | CACCAAGGAGCCCCC[A/G]AGCGCTGAGAGCCCA | 899 |
rs376761785 | snp | A/C | 0.000253746 | 0.0112609 | utr-variant-3-prime, intron-variant | CCNF, LOC105371050 | GRCh38.p7 | 16:2457028 | GGCTGTAAGTGTGTC[A/C]GCACATTTGCCGCAG | 899 |
rs376827215 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2453626 | CCTCACACAGAGAGG[C/T]CCCCAAGGCTTGTCA | 899 |
rs376874490 | snp | A/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2437752 | AAATACAAAAAAGTT[A/G]GCCAGGGGTGGTGGT | 899 |
rs376889526 | snp | A/G | 1.74894e-05 | 0.00295709 | intron-variant | CCNF | GRCh38.p7 | 16:2439850 | CGGGGCTGGGATGAC[A/G]TGGGGAGCTGGCCTT | 899 |
rs376927048 | snp | A/C | 1.658e-05 | 0.00287919 | intron-variant | CCNF | GRCh38.p7 | 16:2453369 | GTGGGCGGGCCTCAC[A/C]CTCGGGGCCTCTGCA | 899 |
rs376935289 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | CCNF, LOC105371050 | GRCh38.p7 | 16:2457613 | CAGGCCCACTCCCTA[C/T]GACACGTGACTCGTT | 899 |
rs376999110 | snp | A/C/G | | | intron-variant, downstream-variant-500B, upstream-variant-2KB | CCNF, C16orf59, LOC105371050 | GRCh38.p7 | 16:2459196 | CCCTCCTTCCCCTCT[A/C/G]CGATGGCACCTTCCC | 899 |
rs377030852 | snp | A/G | 3.45006e-05 | 0.00415321 | synonymous-codon | CCNF | GRCh38.p7 | 16:2449440 | CGCAGCCCTGCTCCT[A/G]GCCAGACTGACGCAC | 899 |
rs377102842 | snp | C/T | 3.30518e-05 | 0.00406507 | missense, nc-transcript-variant | CCNF, LOC105371050 | GRCh38.p7 | 16:2456860 | CCCTGGACAGTGACT[C/T]GCACACACAGCCCTG | 899 |
rs377117663 | snp | A/G | 0.00014227 | 0.00843295 | intron-variant | CCNF | GRCh38.p7 | 16:2439481 | TGCCTGCTCTGGGTC[A/G]GGGGGAGTTATGCTG | 899 |
rs377119279 | snp | A/G/T | 0.000164815 | 0.00907661 | intron-variant | CCNF | GRCh38.p7 | 16:2449949 | CAGAGGCTCATGCCT[A/G/T]TAACCCCAGCACTTT | 899 |
rs377121613 | snp | C/T | 1.69315e-05 | 0.00290955 | missense | CCNF | GRCh38.p7 | 16:2449396 | CTGCACACCAGCCTG[C/T]CCGCCTACGCCCCAG | 899 |
rs377169714 | snp | C/T | | | upstream-variant-2KB, intron-variant | CCNF | GRCh38.p7 | 16:2428798 | TCCCGGCCAGCATCC[C/T]CGCCCAGCAGCGGCT | 899 |
rs377183702 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | CCNF | GRCh38.p7 | 16:2429200 | ACGCGGGTTCCACCA[A/G]TCAGCGGCCAATGTT | 899 |
rs377390030 | snp | C/T | 0.00119559 | 0.0244206 | intron-variant | CCNF | GRCh38.p7 | 16:2439505 | TATGCTGGACAAAGG[C/T]GTAGTTGATGCTGGT | 899 |
rs377394838 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | CCNF | GRCh38.p7 | 16:2448723 | GCTCCATTATGAAGC[C/T]TCTGTTTGTCACCAA | 899 |
rs377522066 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CCNF | GRCh38.p7 | 16:2430531 | CCTGAGCAACAACCT[C/T]ACTGCGTAGCTGTCA | 899 |
rs377612641 | snp | C/T | 4.94238e-05 | 0.00497086 | missense | CCNF | GRCh38.p7 | 16:2449887 | TATGAAGACCTCATT[C/T]CCTGCGTCTTGAGCC | 899 |
rs377617038 | snp | C/T | 0.000100668 | 0.00709392 | intron-variant | CCNF | GRCh38.p7 | 16:2449248 | CAAGGAGCCCCCGAG[C/T]GCTGAGAGCCCACAC | 899 |
rs377668471 | snp | A/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2453805 | GATGGTTTCGAGCAC[A/G]CGGGAGCCTAGCCTG | 899 |
rs377726132 | snp | C/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2434721 | AGAACGTTCTCCTTA[C/T]CCCAAGAAGAAAGCT | 899 |
rs377764848 | in-del | -/A | | | intron-variant, utr-variant-3-prime | CCNF | GRCh38.p7 | 16:2447270 | AATCAACTCTGCCTT[-/A]TTATCTTTTTTTTTT | 899 |
rs386384070 | in-del | -/TT | | | intron-variant, downstream-variant-500B | CCNF, MIR6767 | GRCh38.p7 | 16:2445741 | TTGTTTTTTTTTTTT[-/TT]TCCCGAGACCAAGTC | 899 |
rs386787828 | in-del | AC/CTGTGG | | | intron-variant | CCNF | GRCh38.p7 | 16:2453779 | CTCTGACTGGGCTCC[AC/CTGTGG]AGGAAGATGGTTTCG | 899 |
rs397705371 | in-del | -/T | | | intron-variant, upstream-variant-2KB | CCNF, MIR6767 | GRCh38.p7 | 16:2443937 | CCTTTTTTTTTTTTT[-/T]GAAGTGGAGTCTCGC | 899 |
rs397854957 | in-del | -/T | | | intron-variant, upstream-variant-2KB | CCNF, MIR6767 | GRCh38.p7 | 16:2444914 | TCTTTTTTTTTTTTT[-/T]GAGGCAGGCTGTCTG | 899 |
rs397855780 | in-del | -/C | 0 | 0 | upstream-variant-2KB, intron-variant | CCNF | GRCh38.p7 | 16:2428747 | GCGGGGGAGACTTCC[-/C]AGCGTCAGCTCCGAC | 899 |
rs527349381 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2440131 | AATTTGTGCCATTCT[G/T]GAAAGTTGTCCCATA | 899 |
rs527354294 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2434132 | CCAACATGGCAAAAC[C/T]CTGTCTCTATTAAAA | 899 |
rs527396156 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2434889 | GCTGGCTTCTTTCAC[A/G]GACCCTGATGTTTTC | 899 |
rs527460111 | snp | A/C | 0 | 0 | intron-variant | CCNF | GRCh38.p7 | 16:2451480 | TCCCACCTCTCGGCA[A/C]CCCCACTCCCTGGTC | 899 |
rs527471283 | snp | C/T | 5.01542e-05 | 0.00500745 | missense, downstream-variant-500B | CCNF, LOC105371050 | GRCh38.p7 | 16:2456721 | CCCAAACCCCTGGTC[C/T]GCACCAGCCGGGAGC | 899 |
rs527510153 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2452145 | CTGTGGCAGCCGCCC[C/T]GCACATGTCCCGTGT | 899 |
rs527589620 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | CCNF | GRCh38.p7 | 16:2441746 | GGTCTAAAACTCCTG[A/C]CCTCAAGTAATCTGC | 899 |
rs527661477 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2455178 | GGGCTTCACACCCAG[A/G]CCTGGGGCCTGAGTT | 899 |
rs527743818 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | CCNF | GRCh38.p7 | 16:2433227 | GGTGGCAGACCTCAC[A/G]CATCAGGCCGCACAA | 899 |
rs527865414 | snp | A/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2454738 | ATCTGCCTGGCGCCG[A/G]GCTAAGCACTGCCTG | 899 |
rs527878465 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | CCNF, MIR6767 | GRCh38.p7 | 16:2445809 | CTTGGCTCACCGCAA[C/T]CTCTGCCTCCCAGGT | 899 |
rs527901312 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CCNF | GRCh38.p7 | 16:2430006 | GTGGTTTCAGCTATT[A/G]TCATAGTATCTGTCC | 899 |
rs527907894 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | CCNF, LOC105371050 | GRCh38.p7 | 16:2457674 | TGACCCACAGATGGC[A/G]TCAATGTGAACACCT | 899 |
rs528091230 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2448281 | GTCTTTTAGCAAACT[A/G]AATGCTCAGGGCACT | 899 |
rs528237255 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | CCNF, LOC105371050 | GRCh38.p7 | 16:2457680 | ACAGATGGCGTCAAT[A/G]TGAACACCTCTCTTT | 899 |
rs528269678 | snp | A/C/G/T | 3.76783e-05 | 0.00434024 | intron-variant, upstream-variant-2KB | CCNF, MIR6767 | GRCh38.p7 | 16:2445359 | TGATTCCAGAGCTAG[A/C/G/T]CAGCTTATTTGGTCG | 899 |
rs528328535 | snp | A/T | 0.0107246 | 0.0724382 | intron-variant | CCNF | GRCh38.p7 | 16:2442760 | TAATAATTATAATAA[A/T]ATAATATATATCATA | 899 |
rs528483350 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | CCNF | GRCh38.p7 | 16:2447403 | GCCTGGCCAACATGG[C/T]GAAACCCTGTCTCTA | 899 |
rs528531463 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2441953 | TATATATATATATAT[A/T]TATATATATATATAT | 899 |
rs528755519 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2436027 | GAGCTCGTGCCCAGA[C/T]GTACCCTGCTGAGGG | 899 |
rs528792259 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-5-prime, intron-variant | CCNF | GRCh38.p7 | 16:2429458 | TCTCAGGCGGGCTCC[A/G]GCGGCAGCGACGCGA | 899 |
rs528913150 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2432702 | TGTTGAACCCTCTTT[C/T]TCAGCCTAGGTGTTT | 899 |
rs529050068 | in-del | -/GGT | 0.00318978 | 0.0398085 | intron-variant | CCNF | GRCh38.p7 | 16:2450798 | TGCTTTTGCTCTGGC[-/GGT]GGCTGAGCTCATAGT | 899 |
rs529121551 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2455289 | AACCTTTGGGAGCAC[A/G]TGGTGACAGGCTGGG | 899 |
rs529156518 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2433389 | ACTCAGCCTTCCTTC[C/T]CTTTGGTCAAAACCA | 899 |
rs529186585 | snp | C/T | | | utr-variant-3-prime, upstream-variant-2KB, intron-variant | CCNF, C16orf59, LOC105371050 | GRCh38.p7 | 16:2458517 | GGTCTCCCAAAGTGC[C/T]GGGATTACAGGCATG | 899 |
rs529254347 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B, upstream-variant-2KB | CCNF, C16orf59, LOC105371050 | GRCh38.p7 | 16:2459098 | GGCCACCGTCACCCT[C/T]CCCCACCGCTGATGG | 899 |
rs529342910 | snp | C/G/T | 1.6473e-05 | 0.00286988 | utr-variant-5-prime, synonymous-codon | CCNF | GRCh38.p7 | 16:2431221 | CATCTTGAGTCTCCC[C/G/T]GAAGATGTGCTCTTT | 899 |
rs529400884 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | CCNF | GRCh38.p7 | 16:2431899 | GCAGTAGCGCAATCT[C/T]GGCTCACTGCAAGTT | 899 |
rs529445674 | snp | C/T | 3.39012e-05 | 0.00411697 | synonymous-codon | CCNF | GRCh38.p7 | 16:2449398 | GCACACCAGCCTGTC[C/T]GCCTACGCCCCAGCC | 899 |
rs529469021 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2454684 | GACCCCAGTTGGGTG[G/T]GGGTGTCAGCACCGC | 899 |
rs529602556 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2454227 | AGTGGGCTCCTGGCA[A/G]GAGACCTCAACTCCT | 899 |
rs529759006 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CCNF | GRCh38.p7 | 16:2428288 | CCGGCTGAAGCCTGC[A/T]CGCCAGGGCTCCTGT | 899 |
rs529766156 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CCNF | GRCh38.p7 | 16:2427546 | AAGCTACTTCACTTT[A/C]CCTTCTCTCCCCTGC | 899 |
rs529878523 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | CCNF | GRCh38.p7 | 16:2447509 | GAATTGCTTGAACCC[A/G]AGAGGCAGAGGTTGC | 899 |
rs530057836 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CCNF | GRCh38.p7 | 16:2451227 | CAGCAGGCAGGCGCG[C/T]GGGGCAGGTGGCGCG | 899 |
rs530126325 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | CCNF, MIR6767 | GRCh38.p7 | 16:2445873 | GCTGGGACTGCAGGC[A/G]TGCGCCACCATGCCC | 899 |
rs530225564 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CCNF | GRCh38.p7 | 16:2440204 | GCAGAGGGGCGTGGA[A/G]AGTCCCTTCCTGCTT | 899 |
rs530265024 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CCNF | GRCh38.p7 | 16:2434972 | TTATTAAGAAATGTT[C/T]GACCGAGCGTGGTGG | 899 |
rs530285818 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2439647 | CCACCATTTGAGAGA[C/G]AAGAGGTGGGAAGTT | 899 |
rs530420264 | snp | C/G | 1.64855e-05 | 0.00287097 | missense | CCNF | GRCh38.p7 | 16:2448878 | GTAAAGAGATCCTGA[C/G]CATCCGGGAGGCCGT | 899 |
rs530559226 | snp | A/C/T | 0.0014759 | 0.0271255 | intron-variant | CCNF | GRCh38.p7 | 16:2449222 | CGCTGGGCCTGCATG[A/C/T]GGCACTGCACCAAGG | 899 |
rs530579159 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2453606 | GCCCAGTTCCCTCAG[C/T]GCTTCCTCACACAGA | 899 |
rs530658883 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CCNF | GRCh38.p7 | 16:2432055 | CAGGATGGTCTCTAT[C/T]TCTTGACCTCGTGAT | 899 |
rs530660647 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CCNF | GRCh38.p7 | 16:2437811 | GGCTGCGGTGGGAGG[A/G]TCGCTTGAGCCTGGG | 899 |
rs530785783 | snp | A/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2447855 | GCTGGGCTCTCATTG[A/G]CCACTGACATCTTGT | 899 |
rs530923736 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CCNF | GRCh38.p7 | 16:2436075 | TGACTTTGCAGGTTA[C/T]GAAAGTCGCCTCTTG | 899 |
rs530962466 | snp | G/T | 0.0153668 | 0.0862975 | intron-variant | CCNF | GRCh38.p7 | 16:2429506 | GGCGGCGGTGAGTGC[G/T]GGGCGATGTCCGCTG | 899 |
rs530990344 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2448129 | CGGCCACACAGTGCC[A/G]GGCACAGACTTTCCA | 899 |
rs531108030 | snp | C/T | 0.00159617 | 0.0282053 | utr-variant-3-prime, intron-variant | CCNF, LOC105371050 | GRCh38.p7 | 16:2457824 | ACCATTATTTAGGTT[C/T]ACCTGCAAAACAAAA | 899 |
rs531146892 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, upstream-variant-2KB, intron-variant | CCNF, C16orf59, LOC105371050 | GRCh38.p7 | 16:2458288 | GAGACAGTTTTGCTC[G/T]TGTCTCCCCGGCTGG | 899 |
rs531194758 | snp | A/C | 0.0023933 | 0.0345097 | utr-variant-3-prime, upstream-variant-2KB, intron-variant | CCNF, C16orf59, LOC105371050 | GRCh38.p7 | 16:2458709 | TGTGGTCGGGGTGAG[A/C]ACCCAAGCGTTGGAA | 899 |
rs531201702 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2430240 | TTTCAGGACTGGAAG[A/G]AAGGATGGATAGAAA | 899 |
rs531206169 | snp | C/T | 3.08713e-05 | 0.0039287 | intron-variant | CCNF | GRCh38.p7 | 16:2439492 | GGTCGGGGGGAGTTA[C/T]GCTGGACAAAGGCGT | 899 |
rs531239350 | snp | A/C | 0.000775072 | 0.0196707 | intron-variant | CCNF | GRCh38.p7 | 16:2431089 | TGTGTATATAGAATA[A/C]TTTTTCATCTTATCA | 899 |
rs531334907 | snp | C/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2450912 | GGGATAGAGCTATCC[C/T]CTGTCTCACTGAGAA | 899 |
rs531375971 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2433857 | CTGACAGGGATTCGC[C/T]GTGAGCCTCGTCCAT | 899 |
rs531402944 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CCNF | GRCh38.p7 | 16:2438718 | GTAAAGAATAAGGGC[C/T]GGTCATGGTGGCTCA | 899 |
rs531458604 | in-del | -/T | 0.39709 | 0.20215 | intron-variant | CCNF | GRCh38.p7 | 16:2431836 | AACAAAGAAAGTACC[-/T]TTTTTTTTTTTTGAG | 899 |
rs531519107 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CCNF | GRCh38.p7 | 16:2455639 | GGGCCTCTGGGCACC[C/T]GGCCCTGTGCGAGCG | 899 |
rs531617658 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2454713 | GCCCAAGGCCAGGCC[A/G]TTCCATGCAATCTGC | 899 |
rs531672957 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CCNF | GRCh38.p7 | 16:2432551 | TGGGTGTTGTTCTTT[A/G]CCCTGAGTCCCTGTG | 899 |
rs531811946 | snp | A/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2452551 | AGATAAATTAGAAAC[A/G]TTATTTAGAAACTAC | 899 |
rs531844453 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | CCNF | GRCh38.p7 | 16:2455069 | CCTCAAAAAAAAAAA[A/C]AAAAAAAAAAAAACA | 899 |
rs531998268 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | CCNF, LOC105371050 | GRCh38.p7 | 16:2457180 | CTCCGCGGGAGTCCC[A/G]TGCAAGCCATCAGAA | 899 |
rs532058886 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CCNF | GRCh38.p7 | 16:2429237 | CGCGTCCTGGCGCGG[C/T]CAATGGCGGGTCCCG | 899 |
rs532155074 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, intron-variant | CCNF, LOC105371050 | GRCh38.p7 | 16:2457649 | GCTCTGTCCCAGAGG[C/T]GTTCGTATGTGACCC | 899 |
rs532213171 | snp | C/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2435119 | AGACAGGCGTGGTGG[C/T]GGGCACCTGTGGTCC | 899 |
rs532234364 | snp | A/T | 0.00993419 | 0.0697739 | intron-variant | CCNF | GRCh38.p7 | 16:2442638 | TATATAATATTATAT[A/T]ATATAATATTATTAT | 899 |
rs532234831 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2453098 | GGAACTGCCAGGTCA[A/G]ATTCCAGAGTGACTG | 899 |
rs532235217 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | CCNF | GRCh38.p7 | 16:2447622 | CAGACGTGGTAGTGG[G/T]CGCCTGTAGTCCCAT | 899 |
rs532353542 | snp | A/C | | | intron-variant | CCNF | GRCh38.p7 | 16:2452192 | CGCTGTCCGGCTTCC[A/C]GGATGAGATCAGAAC | 899 |
rs532387753 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CCNF | GRCh38.p7 | 16:2428585 | CAGATACGACACTTC[C/T]CGCGGCGAGCAGCTC | 899 |
rs532548022 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2451925 | CCTTGACCTGCCACC[C/T]CCCTGCCAGCGTGAC | 899 |
rs532565704 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | CCNF | GRCh38.p7 | 16:2440255 | GCTTGTCATGTCACC[G/T]GGTCACCAAGTCATC | 899 |
rs532611430 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | CCNF | GRCh38.p7 | 16:2428570 | CAAGACAAGAGTGAG[C/T]AGATACGACACTTCC | 899 |
rs532611937 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CCNF | GRCh38.p7 | 16:2451247 | CAGGTGGCGCGGGCG[A/G]GGGCGACTCCCTTCA | 899 |
rs532661433 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2441169 | AACCCAGGAGGAGGA[A/G]GTTGCAGTGAGCCGA | 899 |
rs532798980 | in-del | -/A | 0.305934 | 0.243663 | intron-variant | CCNF | GRCh38.p7 | 16:2442889 | ATATTATAATTATAT[-/A]ATTATATATTATATA | 899 |
rs532807846 | in-del | -/TA | 0.00159617 | 0.0282053 | intron-variant | CCNF | GRCh38.p7 | 16:2442312 | CACCCAGCCCTTAAT[-/TA]TATATATATATAATA | 899 |
rs532898317 | snp | A/G | | | missense, downstream-variant-500B | CCNF, MIR6767 | GRCh38.p7 | 16:2445471 | AGGTACATTCTGATC[A/G]ACTGGCTGGTGGAAG | 899 |
rs532945825 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CCNF, MIR6767 | GRCh38.p7 | 16:2444188 | CCTCCCAAAGTGCTG[A/G]GATTACAGGCGTGAG | 899 |
rs533012240 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | CCNF | GRCh38.p7 | 16:2439584 | CGGTCTCTCAGCCTC[C/T]GGGAACCACTGGTCA | 899 |
rs533078433 | in-del | -/CT | 0.00119737 | 0.0244387 | intron-variant | CCNF | GRCh38.p7 | 16:2439220 | GAGAATTGGTTGAAC[-/CT]CCAGGAGGCGGAGGT | 899 |
rs533216370 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CCNF | GRCh38.p7 | 16:2437938 | GACTGAAATCTGGGA[A/G]TGGCCCTCTGCAGGG | 899 |
rs533234618 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2436435 | CCCAAGGAACGAGCC[C/T]ATGATCTGTCCCAGC | 899 |
rs533340702 | snp | C/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2433895 | GCCAGAAATCCAGAT[C/T]GACAGCCAACCAGGG | 899 |
rs533405080 | snp | C/T | 4.94303e-05 | 0.00497119 | intron-variant | CCNF | GRCh38.p7 | 16:2431127 | TGTCTTTTTTTCCTT[C/T]AGTGGTCCACTGTAG | 899 |
rs533431238 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CCNF, MIR6767 | GRCh38.p7 | 16:2443494 | GAATAATAATTAAAA[C/T]CTGAGCCATCCTTGT | 899 |
rs533495240 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, upstream-variant-2KB, intron-variant | CCNF, C16orf59, LOC105371050 | GRCh38.p7 | 16:2458429 | TAATTTTTGTATTTT[C/T]GGTAGAGACGGGATT | 899 |
rs533557214 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2455650 | CACCCGGCCCTGTGC[A/G]AGCGCTGTGGGAGGA | 899 |
rs533752855 | snp | C/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2431596 | GAGGCGGGAAAATTG[C/T]TTGAACCTGGGAGGC | 899 |
rs533883191 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2450967 | TGCGCCGTCGTGCCC[A/G]GATGTGACCCCCTGT | 899 |
rs533910112 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CCNF | GRCh38.p7 | 16:2449973 | GCACTTTGGGAGGCC[A/G]AGGCGGGCAGATCAT | 899 |
rs533918371 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CCNF, MIR6767 | GRCh38.p7 | 16:2444439 | TCAGGAGCTGGGACT[A/G]CAGGTGCCTGCCACC | 899 |
rs533955457 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CCNF, MIR6767 | GRCh38.p7 | 16:2445082 | GGGGCATCATTTACC[A/G]TATTGGGGCATTCCC | 899 |
rs533996698 | snp | C/T | | | intron-variant, downstream-variant-500B, upstream-variant-2KB | CCNF, C16orf59, LOC105371050 | GRCh38.p7 | 16:2459209 | CTGCGATGGCACCTT[C/T]CCATTAACGACTATG | 899 |
rs533999289 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2446509 | TGGATCCCCTAGTTC[C/T]GCCTTTGGAAATAAC | 899 |
rs534000888 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2439862 | GACGTGGGGAGCTGG[A/C]CTTTCTCCCTCCAGC | 899 |
rs534066691 | snp | C/G | 1.78912e-05 | 0.00299086 | intron-variant | CCNF | GRCh38.p7 | 16:2449472 | GGCAGAGTAAGGAGT[C/G]GCCCTTCCCAGGGAT | 899 |
rs534074030 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CCNF | GRCh38.p7 | 16:2454781 | CAACACCAGAGGGGC[C/T]GGGTGCGGTTGCTCA | 899 |
rs534162781 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2433548 | CCACAGCTCAGGCGG[A/G]GATTTTTCTTTTTTG | 899 |
rs534293532 | in-del | -/GCCACTGCGCCT | 0.00557542 | 0.0525036 | intron-variant | CCNF | GRCh38.p7 | 16:2446014 | GGATTACAGGCACAA[-/GCCACTGCGCCT]GGCCCTCACTGGTTC | 899 |
rs534338784 | snp | A/T | 0.151334 | 0.229706 | intron-variant | CCNF | GRCh38.p7 | 16:2442432 | ATAATATAATATTAT[A/T]ATATATAATATATAA | 899 |
rs534453418 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | CCNF | GRCh38.p7 | 16:2447272 | TCAACTCTGCCTTAT[G/T]ATCTTTTTTTTTTTT | 899 |
rs534465527 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2438318 | CCTGGCTCCATGACC[C/T]GCCTGGCAGGGGAGT | 899 |
rs534513041 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2429792 | TCCGGCGATCGGGTC[C/G]CGGGGCGGCGATCGG | 899 |
rs534549622 | snp | A/C | 9.91834e-05 | 0.00704144 | missense | CCNF | GRCh38.p7 | 16:2453474 | GCCCCGACCCCCCGA[A/C]TTTCCTCAGCACAGG | 899 |
rs534572533 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CCNF | GRCh38.p7 | 16:2436188 | TGTGCGCCATGAGCA[C/T]GCAGACCTGCCTGTG | 899 |
rs534654142 | snp | A/G | | | intron-variant, upstream-variant-2KB | CCNF, MIR6767 | GRCh38.p7 | 16:2443431 | GGAAAGGCCACTGAC[A/G]TTTCATTATATATCT | 899 |
rs534707687 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CCNF | GRCh38.p7 | 16:2435026 | TTGGGAGGCCGAGGC[A/G]GGTGGATCATGAGAT | 899 |
rs534744196 | snp | C/G | 0.00557542 | 0.0525036 | upstream-variant-2KB, intron-variant | CCNF | GRCh38.p7 | 16:2427698 | CCACACCCTGGAGGA[C/G]CCACTTATCACCCCA | 899 |
rs534755948 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2452714 | CCCCAACTTCCTCAG[C/T]GCTAGATGACCCCCA | 899 |
rs534910480 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2452311 | CTGGTGGCATCTCCC[A/G]GGCTTTGGCATGTGC | 899 |
rs535018416 | snp | A/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2440515 | CAGGAAGTTGAGGCA[A/G]GAGAATCGCTTGAAC | 899 |
rs535078707 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2434590 | CACTCCAGCCTGAGC[A/G]ACAGAGCGAGACTCC | 899 |
rs535162009 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | CCNF | GRCh38.p7 | 16:2431494 | GACCAGCCTGGCCAA[C/G]TTGGCAAAACCCCCA | 899 |
rs535254452 | snp | C/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2440330 | ACAGCTATAAATAAG[C/T]TGTTAGGGCCAGGTG | 899 |
rs535301844 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | CCNF | GRCh38.p7 | 16:2428735 | GGTCAGCGTTCCGCG[A/G]GGGAGACTTCCCAGC | 899 |
rs535424414 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, upstream-variant-2KB, intron-variant | CCNF, C16orf59, LOC105371050 | GRCh38.p7 | 16:2458439 | ATTTTCGGTAGAGAC[A/G]GGATTTCACCATGTT | 899 |
rs535449480 | snp | C/T | 0.000399281 | 0.0141238 | missense | CCNF | GRCh38.p7 | 16:2453480 | ACCCCCCGACTTTCC[C/T]CAGCACAGGGGAGAT | 899 |
rs535487605 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2448501 | AGCCTCAACTTCCTG[A/G]GCTTAAGCAATCCTC | 899 |
rs535583469 | snp | A/T | 0.00199481 | 0.0315187 | utr-variant-3-prime, intron-variant | CCNF, LOC105371050 | GRCh38.p7 | 16:2457970 | GCAGAAGAGCAGAGC[A/T]GTCGGGGGCCGTGTC | 899 |
rs535792586 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CCNF | GRCh38.p7 | 16:2454438 | CCAGGAGGGGGCCTG[A/G]CCCTGGCCCTGTGCT | 899 |
rs535847894 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2453798 | GGAGGAAGATGGTTT[C/T]GAGCACGCGGGAGCC | 899 |
rs535874598 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | CCNF | GRCh38.p7 | 16:2450773 | CACTGGTTTCCACAT[C/T]GTCTGCTGCTGCTTT | 899 |
rs535989228 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2455690 | CAGAGTGCGGGGTGG[G/T]GCCAGCTCCTGCCCC | 899 |
rs536039715 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CCNF, MIR6767 | GRCh38.p7 | 16:2443898 | CAGTTACCTGTGACA[C/G]GGCGGCATAGAGTTC | 899 |
rs536076193 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | CCNF, MIR6767 | GRCh38.p7 | 16:2444208 | ACAGGCGTGAGCCAC[C/T]GCGCCCAGCCTTGGG | 899 |
rs536237460 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2438403 | TCACTCGTCTGCTGG[C/G]CCTGCTCCTCGTGGG | 899 |
rs536266786 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CCNF | GRCh38.p7 | 16:2438925 | GTTGCTTGAACCCGG[G/T]AAGCTGAGGTTTTAG | 899 |
rs536384102 | in-del | -/A | 0.00438332 | 0.0466095 | intron-variant, upstream-variant-2KB | CCNF, MIR6767 | GRCh38.p7 | 16:2443895 | CCCCAGTTACCTGTG[-/A]CAGGGCGGCATAGAG | 899 |
rs536393374 | snp | A/C | | | intron-variant | CCNF | GRCh38.p7 | 16:2446377 | GAGTTTTTCGTCCCC[A/C]ACTGGTGCCCTGCAG | 899 |
rs536443758 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2440522 | TTGAGGCAGGAGAAT[C/T]GCTTGAACCCGGGAG | 899 |
rs536506399 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CCNF | GRCh38.p7 | 16:2433626 | GGAGTCTCGCTCTGT[C/T]ACCAGGCTGGAGTGC | 899 |
rs536587278 | snp | A/G | 0.000107333 | 0.00732494 | intron-variant | CCNF | GRCh38.p7 | 16:2455574 | GCGACGGTGAGTGTG[A/G]GGCCAGGGTGCACCA | 899 |
rs536642249 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2436243 | CCTCTTAGAACTCTC[A/G]AGACAGAGTTCAGCG | 899 |
rs536701168 | snp | A/T | 0.0232847 | 0.105357 | intron-variant | CCNF | GRCh38.p7 | 16:2442435 | ATATAATATTATTAT[A/T]TATAATATATAATAT | 899 |
rs536821997 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | CCNF, LOC105371050 | GRCh38.p7 | 16:2458009 | TCCCAACTGCAGCTC[C/T]GCTGTGGGGGCCCGT | 899 |
rs536915893 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2437049 | CTTCAGGCATTACAC[A/T]TTCCACCAAGACCAT | 899 |
rs536951280 | snp | A/G | 0.00031341 | 0.0125143 | intron-variant | CCNF | GRCh38.p7 | 16:2431287 | GGCCGTCCGAGCTGT[A/G]AGTCCCTGCATGAAA | 899 |
rs537041791 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | CCNF | GRCh38.p7 | 16:2442937 | AATATATATGATTAT[A/T]ATATATTATTATATT | 899 |
rs537137213 | in-del | -/GGG | 0.00517822 | 0.0506191 | intron-variant | CCNF | GRCh38.p7 | 16:2451586 | TTCCTTTTTTGAGTT[-/GGG]GGCCCAGGCTGGAGT | 899 |
rs537152093 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CCNF | GRCh38.p7 | 16:2428894 | GTGAGGGTCGCGGGC[C/T]CAGGAGCGACCCCGG | 899 |
rs537268129 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2447890 | TTGGCGTCTGCAGCC[C/T]CCACGCTGGCAGGTG | 899 |
rs537335252 | in-del | -/AATAATAA | 0.00279162 | 0.0372561 | intron-variant | CCNF | GRCh38.p7 | 16:2434312 | CTGTCTCAAAAAAAT[-/AATAATAA]AATAATAAAATATGG | 899 |
rs537427531 | snp | A/G | | | intron-variant, upstream-variant-2KB | CCNF, MIR6767 | GRCh38.p7 | 16:2443598 | GCTTCAGAAATGGAA[A/G]ACTGCAACATGGCTG | 899 |
rs537518989 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CCNF | GRCh38.p7 | 16:2428008 | CCTCTGCCCTAGGGG[A/G]AGACAGGTAACAGTG | 899 |
rs537679553 | in-del | -/T | 0.327445 | 0.237702 | intron-variant, utr-variant-3-prime | CCNF | GRCh38.p7 | 16:2447276 | CTCTGCCTTATTATC[-/T]TTTTTTTTTTTTTTT | 899 |
rs537715211 | in-del | -/C | | | intron-variant | CCNF | GRCh38.p7 | 16:2431679 | AGCGAGACTCTGTCT[-/C]AAAAAAAAAAAAAAA | 899 |
rs537789131 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CCNF | GRCh38.p7 | 16:2452418 | GGTTCGCATGGGTCT[C/T]GTCCCACCCACCTTT | 899 |
rs537834175 | snp | A/G | 4.1389e-05 | 0.00454893 | intron-variant | CCNF | GRCh38.p7 | 16:2449108 | TCTCTGCTGTGCCCA[A/G]AGCCATGGAGCAGGA | 899 |
rs537867107 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CCNF, MIR6767 | GRCh38.p7 | 16:2443917 | GGCATAGAGTTCCCT[C/T]ATCACCCTTTTTTTT | 899 |
rs537870896 | snp | C/G/T | 8.72782e-05 | 0.00660548 | missense | CCNF | GRCh38.p7 | 16:2449451 | TCCTGGCCAGACTGA[C/G/T]GCACGGGCAGAGTAA | 899 |
rs537908514 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CCNF | GRCh38.p7 | 16:2432820 | ACAGTTACTTTCACA[C/T]AGAGATTGGGGACCT | 899 |
rs537990831 | snp | A/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2455154 | CCCCACAGCTGAGCC[A/G]GGTGGGCTGGGCTTC | 899 |
rs538024859 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2450460 | AGGTTGCGGTGAGCC[A/G]AGATTGCGCCATTGC | 899 |
rs538045327 | snp | C/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2454037 | CCGCCTGGAGAACTC[C/G]TACTGATTCCACAAG | 899 |
rs538046634 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CCNF, MIR6767 | GRCh38.p7 | 16:2444835 | CTCCTGGGCTCAAGC[A/G/T]AACCTCCTGCCCCAG | 899 |
rs538085033 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2438205 | TGAAAAGCAGCAGAA[G/T]GGGGTGTCCAAGGCC | 899 |
rs538259821 | snp | G/T | | | upstream-variant-2KB, intron-variant | CCNF | GRCh38.p7 | 16:2427649 | GACTTTTCCAACAAG[G/T]TCTCACCTTCCTGAA | 899 |
rs538271552 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | CCNF | GRCh38.p7 | 16:2447127 | CCTACGACAAAGCTC[C/T]TGGGCCACAACCGGC | 899 |
rs538321186 | snp | C/T | | | intron-variant | CCNF | GRCh38.p7 | 16:2454458 | GGCCCTGTGCTCAGC[C/T]TCGCTGTGTTAAACC | 899 |
rs538384129 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2451671 | TTCTTTTGTGTCAGC[A/C]TCCCGAGTAGCAGAA | 899 |
rs538423296 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2437687 | TGTGGCCAGGTGTTC[A/G]AGACCAGTCTGGGCA | 899 |
rs538444194 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | CCNF | GRCh38.p7 | 16:2435615 | TATATATATATATGC[A/C]CACACACACACACAT | 899 |
rs538484045 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CCNF, MIR6767 | GRCh38.p7 | 16:2444393 | CAAGCTCCACCTCCC[A/G]GGTTCACACCATTCT | 899 |
rs538507571 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2441537 | TTTGGGAGGCTGAGG[C/T]GGGAGGATCACTTGA | 899 |
rs538602237 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2453775 | CTCGCTCTGACTGGG[A/C]TCCCTGTGGAGGAAG | 899 |
rs538660211 | in-del | -/TAT | 0.354235 | 0.227234 | intron-variant | CCNF | GRCh38.p7 | 16:2442781 | ATATATCATATATAA[-/TAT]TATATATTATATTCT | 899 |
rs538709929 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2446014 | GGATTACAGGCACAA[A/G]CCACTGCGCCTGGCC | 899 |
rs538853330 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CCNF | GRCh38.p7 | 16:2436169 | CTGTTTGGGCTCCCT[C/G]CCCTGTGCGCCATGA | 899 |
rs538863564 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CCNF | GRCh38.p7 | 16:2428961 | ACGTCGAGGCTGTCC[A/C]AGGCTGGATCACGGC | 899 |
rs538947913 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CCNF | GRCh38.p7 | 16:2427678 | AAGCCCAGTGGGAAA[C/T]GGGCCCACACCCTGG | 899 |
rs539202338 | snp | C/T | | | upstream-variant-2KB, intron-variant | CCNF | GRCh38.p7 | 16:2429158 | GCTCCTACGGGACCC[C/T]AGCCCCGTTGGGGAG | 899 |
rs539251324 | snp | C/G | | | intron-variant | CCNF | GRCh38.p7 | 16:2437485 | CGCATCTGGAAATCA[C/G]CTGGCACAGAGGAGG | 899 |